NZ200759A - Producing hydrogen-and carbon monoxide-containing gas mixtures by partial oxidation of carbonaceous fuels - Google Patents
Producing hydrogen-and carbon monoxide-containing gas mixtures by partial oxidation of carbonaceous fuelsInfo
- Publication number
- NZ200759A NZ200759A NZ200759A NZ20075982A NZ200759A NZ 200759 A NZ200759 A NZ 200759A NZ 200759 A NZ200759 A NZ 200759A NZ 20075982 A NZ20075982 A NZ 20075982A NZ 200759 A NZ200759 A NZ 200759A
- Authority
- NZ
- New Zealand
- Prior art keywords
- burner
- fuel
- flow
- annular
- central
- Prior art date
Links
- 239000000446 fuel Substances 0.000 title claims description 342
- 239000000203 mixture Substances 0.000 title claims description 147
- 238000007254 oxidation reaction Methods 0.000 title claims description 41
- 230000003647 oxidation Effects 0.000 title claims description 35
- 229910002091 carbon monoxide Inorganic materials 0.000 title description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title 1
- 239000007789 gas Substances 0.000 claims description 229
- 239000001301 oxygen Substances 0.000 claims description 146
- 229910052760 oxygen Inorganic materials 0.000 claims description 146
- 239000002002 slurry Substances 0.000 claims description 117
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 claims description 113
- 239000007788 liquid Substances 0.000 claims description 108
- 239000007787 solid Substances 0.000 claims description 106
- 238000006243 chemical reaction Methods 0.000 claims description 93
- 239000000376 reactant Substances 0.000 claims description 84
- 239000000463 material Substances 0.000 claims description 66
- 238000011144 upstream manufacturing Methods 0.000 claims description 62
- 229910001868 water Inorganic materials 0.000 claims description 57
- 239000012530 fluid Substances 0.000 claims description 52
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 43
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 34
- 229910052799 carbon Inorganic materials 0.000 claims description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 238000013461 design Methods 0.000 claims description 31
- 238000002156 mixing Methods 0.000 claims description 30
- 239000004215 Carbon black (E152) Substances 0.000 claims description 25
- 229930195733 hydrocarbon Natural products 0.000 claims description 25
- 150000002430 hydrocarbons Chemical class 0.000 claims description 25
- 230000003247 decreasing effect Effects 0.000 claims description 21
- 239000003245 coal Substances 0.000 claims description 16
- 238000002485 combustion reaction Methods 0.000 claims description 11
- 230000000153 supplemental effect Effects 0.000 claims description 10
- 238000007599 discharging Methods 0.000 claims description 7
- -1 and Substances 0.000 claims description 5
- 239000008246 gaseous mixture Substances 0.000 claims description 5
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 239000000571 coke Substances 0.000 claims description 3
- 239000003077 lignite Substances 0.000 claims description 3
- 239000004058 oil shale Substances 0.000 claims description 3
- 239000002006 petroleum coke Substances 0.000 claims description 3
- 238000011161 development Methods 0.000 claims description 2
- 244000093965 Triphasia trifolia Species 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000010802 sludge Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 description 29
- 238000001816 cooling Methods 0.000 description 26
- 239000000047 product Substances 0.000 description 19
- 230000015572 biosynthetic process Effects 0.000 description 17
- 238000003786 synthesis reaction Methods 0.000 description 16
- 239000002737 fuel gas Substances 0.000 description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- 229910002092 carbon dioxide Inorganic materials 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 9
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 8
- 238000004891 communication Methods 0.000 description 8
- 230000001276 controlling effect Effects 0.000 description 8
- 238000006073 displacement reaction Methods 0.000 description 8
- 239000007800 oxidant agent Substances 0.000 description 8
- 230000001590 oxidative effect Effects 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 239000011368 organic material Substances 0.000 description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 6
- 229910010271 silicon carbide Inorganic materials 0.000 description 6
- 239000004449 solid propellant Substances 0.000 description 6
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000010426 asphalt Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 239000002826 coolant Substances 0.000 description 4
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 125000006850 spacer group Chemical group 0.000 description 4
- 238000009834 vaporization Methods 0.000 description 4
- 230000008016 vaporization Effects 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000010791 quenching Methods 0.000 description 3
- 230000000171 quenching effect Effects 0.000 description 3
- 239000004071 soot Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 2
- 239000003830 anthracite Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 229910002090 carbon oxide Inorganic materials 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000001311 chemical methods and process Methods 0.000 description 2
- 239000011280 coal tar Substances 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- 238000004231 fluid catalytic cracking Methods 0.000 description 2
- 239000002803 fossil fuel Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 239000003502 gasoline Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000003915 liquefied petroleum gas Substances 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 239000010742 number 1 fuel oil Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 238000013021 overheating Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000010801 sewage sludge Substances 0.000 description 2
- 239000003079 shale oil Substances 0.000 description 2
- 238000011064 split stream procedure Methods 0.000 description 2
- 239000011269 tar Substances 0.000 description 2
- 239000011275 tar sand Substances 0.000 description 2
- 230000003685 thermal hair damage Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- 101100494773 Caenorhabditis elegans ctl-2 gene Proteins 0.000 description 1
- 101100112369 Fasciola hepatica Cat-1 gene Proteins 0.000 description 1
- 101100005271 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cat-1 gene Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000007514 turning Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/466—Entrained flow processes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
- C10J3/485—Entrained flow gasifiers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
- C10J3/485—Entrained flow gasifiers
- C10J3/487—Swirling or cyclonic gasifiers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
- C10J3/50—Fuel charging devices
- C10J3/506—Fuel charging devices for entrained flow gasifiers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/723—Controlling or regulating the gasification process
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/74—Construction of shells or jackets
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/74—Construction of shells or jackets
- C10J3/76—Water jackets; Steam boiler-jackets
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/78—High-pressure apparatus
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/82—Gas withdrawal means
- C10J3/84—Gas withdrawal means with means for removing dust or tar from the gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/093—Coal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/0943—Coke
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/0946—Waste, e.g. MSW, tires, glass, tar sand, peat, paper, lignite, oil shale
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0953—Gasifying agents
- C10J2300/0956—Air or oxygen enriched air
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0953—Gasifying agents
- C10J2300/0959—Oxygen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0953—Gasifying agents
- C10J2300/0973—Water
- C10J2300/0976—Water as steam
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/18—Details of the gasification process, e.g. loops, autothermal operation
- C10J2300/1807—Recycle loops, e.g. gas, solids, heating medium, water
- C10J2300/1823—Recycle loops, e.g. gas, solids, heating medium, water for synthesis gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/18—Details of the gasification process, e.g. loops, autothermal operation
- C10J2300/1846—Partial oxidation, i.e. injection of air or oxygen only
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
Description
% %
200759
Priority Dsisfa): .
Compfeto Specification Fnsd:% /v; £?•
Class: C-l?^^ {.£?-. . * J^\j
Publication Date: ■
P.O. Journal, Net:
Patents form No. 5 •
Patents Act 1953
J COMPLETE SPECIFICATION
"Partial Oxidation Process"
WE, TEXACO DEVELOPMENT CORPORATION, a Corporation organised and existing under the laws oi' the State of Delaware, United States of' America, of 2000 Westchester Avenue, White Plains, New York, 10650, United States of America, hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly descrined in and by the following statement
\
20P759
PARTIAL OXIDATION PROCESS
This invention relates to the manufacture of gaseous mixtures comprising and CO, e.g., synthesis gas, fuel gas, 5 ana reducing gas by the partial oxidation of pumpable slurries P. L. B. & A. 0£ solid carbonaceous fuels in a liquid carrier and/or liquid li-rp (.her<\oafter -to <m 'KvicIroca/bcAatcenfi pai* QS...... or gaseous hydrocarbon fuels. In one of its more specific aspects, the present invention pertains to switching from one type of fuel to another without interruption of the 10 process.
In the operation of a partial oxidation synthesis gas generator when the principal fuel becomes unavailable or in short supply and it is desired to operate the gas generator with a substitute or stand-by fuel, then previously 15 it was necessary to depressurize the system and shut down the gas generator while the burner is changed and other adjustments are made to the system to provide for the new fuel.
By the subject process, such costly down-time is avoided.
Annulus-type burners have been employed for introducing 20 liquid hydrocarbonaceous fuels into a partial oxidation gas generator. For example, U.S. Patent 3,528,930 shows a single annulus burner, and U.S. Patents 3,758,037 and 3,847,564 show double annulus burners. To obtain proper mixing, atomization, and stability of operation a burner is sized for a 25 specific throughput. Should the type of fuel feedstream car required output of product gas change substantially, ordinarily shut-dov.Ti of the systen is required to replace one burner with another. Such costly shut-downs are avoided by the subject process and control system. The more complex process for preheating a gas generator by means 30 of a preheat burner, removing the preheat burner from the gasifier, and inserting a separate production burner is described in U.S. Patent No. 4,113,445.
A partial oxidation process and control system for continuously producing synthesis gas, fuel gas or reducing 35 gas while changing from one type of fuel to another without -—"7"' " shutting down or depressurizing the gas generator is described.
— .-rl"
■ This multifuel process is not tied to one particular fuel and reacts slurries of solid carbonaceous fuel and/or liquid or
200759
#'
gaseous hydrocarbonaceous fuels. Problems of fuel availability are reduced due to the wide selection of fuels that are suitable for the subject process. By the subject process the total output from the partial oxidation gas generator may be maintained substantially constant while the feed is changed from one fuel to another.
f.L B & a T^e sukject invention pertains to a process for producing gaseous mixtures comprising Hj/ CO, CO^/ entrained particulate t"rZ carbon, and at least one material from the group consisting f IQ /3N flr
of 1^0, N£, H2S, COS, CH^, A^, and ash in a free-flow non-
catalytic partial oxidation gas generator, including employ-P L B & a a °ne °r two~sect^on burner having at least one first
11 fluid conduit or group of conduits to provide a first fluid
H"?"1 aA\ace*^r
D^r MT~
UJtlG LZ*
AajaceAT
passage or passages, and at least one goiatod radially spaced '15 second fluid conduit surrounding said first fluid conduit or group of conduits to provide at least one annular second fluid passage therebetween and having either a central or a central and annular exit orifice at the tip of the burner, and changing from one reactant feedstream to another without 20 shutting down or depressurizing the system, the process comprising the combination of the steps of:
r* , dba (1) passing a first reactant stream of first solid
P. L. d. « "•
,/—• carbonaceous fuel slurry or hydrocarbonaceous fuel with or
_nar -
r ifM without mixture with a temperature moderator through either » /" fluid posso^«s at Ieasr orve of- soUd s«eov»d ftuiol
at least one of said first or cocond fluid paGsagssf f«6sajcsj
(2) simultaneously passing a separate reactant stream of free-oxygen containing gas with or without mixture with
*
a temperature moderating gas through the unused passage or it passages in said burner which are rolatod to a passage
. L. B. & A30 through which said first reactant stream in (1) is flowing; p^r_tb- (3) mixing together said reactant streams from (1)
oL*CI Q> / and (2) to produce a well-distributed blend, and reacting said mixture by partial oxidation in the reaction zone of' said gas generator at an autogenous temperature in the range 35 of about 1700° to 3500°F., a pressure in the range of about to 300 atmospheres, an atomic ratio of oxygen/carbon in the —- '—-fange of about 0.5 to 1.7, and a weight ratio H20/fuel in the r 2 range of about 0 to 5.0;
(4) phasing out of the fluid passage or passages in which it is flowing in said burner said stream of first solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with a temperature moderator, said
phasing out being with a uniformly decreasing rate of flow that varies from maximum to 0 over a period of time in the range of about 1-3600 seconds; and simultaneously phasing said stream of second solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with 10 temperature moderator into the same fluid passage in said burner at a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time, and mixing the phased-in stream with the remaining portion of said stream of first solid carbonaceous fuel slurry or 15 hydrocarbonaceous fuel with or without mixture with a temperature moderator flowing therein; and
(5) adjusting the flow rate of the reactant stream of free-oxygen containing gas with or without mixture with a temperature moderator passing through the burner and if
necessary introducing supplemental 1^0 into the reaction zone, so as to adjust the free oxygen/carbon atomic ratio and the weight ratio I^O/fuel in the reaction zone to design conditions for the partial oxidation reaction.
Manual or automatic control means are included for 25 switching and controlling the fuel, oxidant, and steam streams. By this means, the principal and stand-by fuels may be switched and the stream of free-oxygen containing gas and/or temperature moderator may be controlled up or down - to maintain the gasifier output while retaining 30 efficiency and stability.
in order to illustrate the invention in greater detail, reference is made to several embodiments as shown in the figures of the drawing wherein:
Fig. 1 is a schematic representation of one embodiment 35 of the invention showing control means for replacing one fuel with another while maintaining continuous operation;
Figs. 2 and 3 are vertical longitudinal schematic representations of two preferred burners for use in the subject process;
. Fig." 4 is. a schematic representation of another embodiment of the invention; and 300 s
Fig. 5 is a vertical, longitudinal schematic representation of a two section burner suitable for the subject process.
The present invention pertains to a continuous process for the manufacture of gas mixtures comDrisina H?, P.L.B.SA. 2
,, CO, CO.,, particulate carbon and at least one material
P *rJX7r z ' f\r ■
£$/ £ i ^ selected from the group consisting of H20, , K2S'
COS, and ash such as synthesis gas, fuel gas, and reducing 10 gas, by the partial oxidation of one reactant stream of fuel which is then replaced by a different reactant stream of fuel without shutting down or depressurizing the cas generator. Further, there may be substantially no change in the amount of gas produced. This multifuel process is not restricted to 15 one particular fuel. Problems of fuel availability are reduced. The two reactant fuel streams may be selected from the group consisting of a pumpable slurry of solid carbonaceous
P-L. B.&A.
- fuel in a liquid carrier, jfc-iauid or gaGCOuo hydrocarbonaceous
P«rJ£>_
£$^1 g fuel, and mixtures thereof with or without admixture with a 20 temperature moderator. The fuels are reacted by partial oxidation with a reactant stream of free-oxygen containing gas with or without admixture with a temperature moderator. The product gas mixture is produced in the reaction zone of a noncatalytic, refractory-lined, free-flow partial oxidation 1 25 gas generator, such as described in coassigned U. S. Patent
No. 2,809,104 issued to Dale M. Strasser et al at a temperature in the range of about 17 00 to 3500°F. and a pressure in the range of about 1 to 300 atmospheres, such as about 5 to 250 atmospheres, say about 10 to 100 atmospheres.
^ - \ -[yf Cw-,
~3'0 , During operation of the partial oxidation cas
.generator, it may be necessary to change from one fuel
■ - -)
^ y y 7 -5 9
^ e - -
to another without replacing the burner and without sacrificing stable operation and efficiency. Changing the burner requires a costly shut-down period with resultant delay. Further, the burner should operate with a variety of liquid, solid, and gaseous fuels, and mixtures thereof. Combustion instability and poor efficiency can be encountered when certain prior art burners are used for the gasification of liquid phase slurries of solid carbonaceous fuels. Further, feedstreams may be poorly mixed and solid fuel particles may pass through the gasifier without contacting significant amounts of oxygen. Unreacted oxygen in the reaction zone may then react with the product gas.
A novel burner that may be employed in the subject process is shown in Fig. 2 of the drawing and comprises: a retracted central conduit means coaxial with the central longitudinal axis of the burner and having an upstream inlet through which a first feedstream may be separately introduced and a downstream discharge outlet means; an outer coaxial conduit concentric with said central conduit and having an upstream inlet through which a second feedstream may be separately introduced,
and a converging at least partially frusto-conical shaped exit nozzle terminating said outer conduit at the downstream tip of the burner; wherein said central conduit downstream discharge outlet means is retracted upstream from the downstream" face of the burner a distance of two or more times say 3 to 10 times the minimum diameter of said outer conduit downstream exit nozzle to provide a pre-mix zone; and means for radially spacing said central and outer conduits from each other to provide a coaxial annular
- Q ^
2C:07 59
passage through which said second feedstream may separately pass concurrently with said first feedstream into said.
pre-mix zone where a multiphase mixture is produced prior to being discharged through said outer conduit exit nozzle.
Another novel burner that may be employed in the subject process is shown in Fig. 3 of the drawing and comprises: a central conduit coaxial with the central longitudinal axis of the burner and having an upstream inlet through which a first feedstream may be introduced and a 10 circular downstream discharge outlet, and said central conduit discharge outlet is retracted upstream from the downstream face of the burner a distance of 3 to 10 times the minimum diameter of an outer conduit downstream exit nozzle to be further described so as to provide a pre-mix zone comprising 2 to 5 cylindrically shaped pre-mix chambers in serie and coaxial with the central longitudinal axis of said burner; an intermediate coaxial conduit concentric with said central conduit and having an upstream inlet through which a second feedstream may be introduced, and a converging at least partiall; 20 frusto-conical shaped downstream exit nozzle terminating said intermediate conduit, and the tip of said intermediate conduit exit nozzle is retracted upstream from the downstream face of the burner a distance of 1 to 5 times the minimum diameter of said outer conduit downstream exit nozzle; an outer coaxial conduit concentric with said central and intermediate conduits ana having an upstream inlet through which a third feedstream may be introduced,
and a converging downstream exit nozzle terminating said outer conduit and comprising a frusto-conical shaped rear portion and 30 a right cylindrical shaped front portion at the downstream
tip of the burner; and means for radially spacing said central, intermediate, and outer conduits with respect to each other to provide intermediate and outer coaxial annular passages, and said intermediate annular passage is situated between the outside diameter of the central conduit and the inside diameter of the intermediate conduit and is the passage through which said second feedstream may separately pass concurrently with said first feedstream into a pre-mix zone where a multiphase mixture of said 10 first and second feedstreams is produced, and said outer annular passage is situated between the outside diameter of said intermediate conduit and the inside diameter of said outer conduit and is the passage through which said third feedstream may separately pass concurrently with said first and second feedstreams and then mix with said multiphase mixture of said first and second feedstreams upstream from the downstream face of the burner. Optionally, the walls of said intermediate conduit may contain a plurality of small diameter holes or passages in a 20 plurality of circumferential rings along its length to permit at least a portion of said third feedstream flowing in said outer annular conduit to pass through and mix with one or more of the other materials simultaneously flowing at a lower pressure through the other passages or pre-mix zone of the burner. Optionally, blocking means may be provided at the downstream outlet of said outer annular passage for completely or partially closing the downstream outlet of said outer annular passage. The blocking means may comprise an annular plate disposed perpendicular to 30 the central longitudinal axis of the burner with or
-s -
2007 —
without a plurality of small diameter holes. Said third feedstream may be a temperature moderator selected from the group consisting of 1^0, CC^j Ng and mixtures thereof. Alternatively, a recycle portion of cooled and cleaned product gas or a stream of free-oxygen containing gas may comprise the third feedstream.
Thus,' in this embodiment of the burner, as shown in Pig. 3» a plurality of high pressure high velocity jet streams of said third feedstream may be passed through tl^p 10 walls of the intermediate conduit and into the annular passage and pre-mix chambers at various locations along their length. By this means atomizing of the fuel feedstream and, optionally, mixing it with the oxidant stream may be facilitated. For example, the third feedstream may be passed through a plurality of small diameter passages or holes i.e. about .032 to 0.50 diameter that lead into said annular passage and pre-mix chambers.
In other embodiments an annular-type burner such as shown and described in coassigned U. S. Patent 3*87^,592 20 was employed. Further, the central and/or annular conduit means may include a plurality of parallel or helical tubes.
Alignment pins, fins, centering vanes, spacers and other conventional means are used to symmetrically space the burner conduits with respect to each other and to hold same in stable alignment without obstructing the free-flow of the feedstreams in the central conduit means and annular passage means.
The outer and/or intermediate conduit exit nozzle may comprise a frusto-conical rear portion having a 30 converging angle in the range of about 15° to 90° from the
100 7 5 9
central longitudinal axis of the burner. The rear portion may develop into a normal cylindrical front portion which terminates at the downstream face of the burner. The cylindrical front portion may have a height in the range of about 0 to 1.5 times its own diameter. In one embodiment, the outer conduit exit orifice is in the shape of or is generated by an American Society of Mechanical Engineer's standard long-radius nozzle. A further description of said nozzle may be found in "Thermodynamics Fluid Flow and Heat 10 Transmission" by Huber 0. Croft, page 155> First Edition, 1938 McGraw-Hill Book Company.
The burner may be cooled on the outside by means of cooling coils that encircle the outside barrel of the burner along its length. The downstream end of the burner may be provided with a cored face plate through which a coolant is circulated. For example, an annular cooling chamber may encircle the outer conduit downstream exit nozzle. The cooling chamber and the outer conduit exit nozzle may constitute a single piece of thermal and wear 20 resistant material such as tungsten carbide or silicon carbide. Any suitable coolant may be employed e.g. water. Preferably, the downstream end of the central conduit means may be retracted upstream from the entrance to the first pre-mix chamber in the line. For example, the set back of the end of the central conduit means from the entrance to the first pre-mix chamber may be in the range of about 0.1-2.0 times the diameter of the first pre-mix chamber.
In one embodiment, each of the pre-mix chambers in the central conduit except the first are cylindrical
- to /
shaped and comprises a coaxial cylindrical body portion followed by a coaxial at least partially converging outlet portion. The first cylindrical-shaped pre-mix chamber in the central conduit comprises a normal coaxial cylindrical body portion that discharges directly into the next in line coaxial cylindrical shaped pre-mix chamber. The converging outlet portions of said pre-mix chambers may be made from tungsten carbide or silicon carbide for increased wear resistance.
The size relationship between successive pre-mix chambers in the subject burners may be expressed in the following manner: For burners in which the pre-mix chambers in the central conduit means are successively numbered 1 to
then the ratio of the diameter of any one of said central chambers to the diameter of the next central chamber in the line i.e. D.. :D_; D_:D_; D-, D,, D,. :DC may
1 2 2 3 3;i+jor 4 5
be in the range of about 0.2-1.2. The ratio of the length of any one central pre-mix chamber in said central conduit means to the length of the next central pre-mix chamber in 20 the line i.e. 1^:1^ J or L^:L^ may be in the range of about 0.1-1.0.
In the operation of the embodiment of the burner employing pre-mix chambers flow control means may be used to control the flow of the feedstreams to the passages in the burner in the same manner as described previously. The feedstreams entering the burner and simultaneously ana concurrently passing through at different velocities impinge and mix with each other in the first pre-mix chambers. The impingement of one reactant stream, such 30 as the liquid slurry of solid carbonaceous fuel in a
"II'
• ■ .u: 2 007 5 9
liquid medium optionally in admixture with a temperature moderator, with another reactant stream, such as a gaseous stream of free-oxygen containing gas optionally in admixture with a temperature moderator at a higher velocity, causes the liquid slurry to break up into a fine spray. The multiphase mixture produced then successively passes through any remaining pre-mix chambers where additional mixing takes place. As the mixture passes freely through the subject unobstructed burner its velocity changes many times. For 10 example, at various points in the burner the velocity of the mixture may range from about 20 to 600 ft. per sec. As the mixture flows from one pre-mix chamber to the next, the velocity changes are mainly the result of changes in the diameter of the flow path and the temperature of the mixture. This promotes a thorough mixing of the components. By operating in the region of turbulent flow, mixing may be maximized. Further, direct heat exchange between the materials takes place within the burner. From 0-100 vol. %, say about 5-25 vol. % of the liquids in the feedstreams 20 may be vaporized before the feedstreams leave the burner. By means of converging exit orifices, the feedstreams may be accelerated directly into the reaction zone of the partial oxidation gasifier.
Burning of the combustible materials while passing through the pre-mix zone of the burner may be prevented by discharging the multiphase mixtures at the outer conduit exit nozzle at the tip of the burner with a discharge velocity which is greater than the flame propagation velocity. Flame speeds are a function of such factors as 30 composition of the mixture, temperature and pressure. They may be calculated by conventional methods or determined
-IX -
2 007^9.
-
experimentally. Advantageously, by means of the subject burner, the exothermic partial oxidation reactions take place a sufficient distance downstream from the burner face so as to protect the burner from thermal damage.
Depending on such factors as the temperature, velocity, dwell time and composition of the feedstreams; the desired amount of vaporization of liquid carrier; the temperature and amount of recycle gases in the generator; and the desired life of the burner; cooling coils may or 10 may not encircle the outside barrel of the burner along its length. For similar reasons, the burner may or may not be provided with an annular shaped cooling chamber at the downstream end.
Liquid hydrocarbon fuels and/or pumpable slurries of solid carbonaceous fuels having a dry solids content in the range of about 30 to 75 wt. f3 say about 40 to 70 wt. % may be passed through the inlet passages of the subject burner. For example, the fuel streams with or without mixture with the temperature moderator i.e. HgO may be 20 passed through the central conduit means or through the annular passage means. The inlet temperature of the liquid hydrocarbon fuel or the slurry is in the range of about ambient to 500°F., but preferably below the vaporization temperature of the liquid hydrocarbon at the given inlet pressure in the range of about 1 to 300 atmospheres, such as 5 to 250 atmospheres, say about 10 to 100 atmospheres. Simultaneously the free-oxygen containing gas with or without mixture with the temperature moderator is passed through the corresponding unoccupied passage in the burner. 30 Thus, if the principal or first fuel flowing through a central conduit means of the burner or through
0759
the coaxial annular passage means of the burner becomes unavailable and it is desired to switch to a stand-by or second fuel, or for any reason whatsoever it is desired to switch from a first solid carbonaceous fuel slurry or hydrocarbonaceous fuel to a second solid carbonaceous fuel slurry or hydrocarbonaceous fuel without shutting down or depressurizing the system, one may proceed as follows:
(1) separately sensing the flow rates of four feedstreams 1-4 respectively consisting of steam, stand-by
fuel, principal fuel, and free-oxygen containing gas, and providing signals s, m, a, and b corresponding respectively to the actual flow rates of feedstreams 1-4 to a control unit;
(2) comparing said actual flow rate signals s, m,
a, and b respectively with manual or automatically computed and inserted input signals representing the desired flow rate or set point for that moment for each of the four feedstreams, and providing a corresponding adjustment signal to a flow rate control means for controlling the flow rate of each feedstream 1-4 in accordance with the respective
set point of each;
(3) passing a feedstream of said principal fuel into the reaction zone of a free-flow noncatalytic partial oxidation gas generator, by way of a burner comprising a central conduit means radially spaced from a concentric coaxial outer conduit means having a downstream exit nozzle and providing a coaxial annular passage means therebetween and wherein said feedstream of principal fuel is passed through either the central conduit means of the burner or through the coaxial annular passage means;
(4) simultaneously passing a separate feedstream of free-oxygen containing gas with or without mixture with
a separate feedstream of steam through the unoccupied fluid passage means in said burner;
(.51 mixing together said reactant streams from (31 and (_4)_ to produce a well-distributed blend, and reacting said mixtures by partial oxidation in the reaction zone of said gas generator at an autogenous temperature in the range of about 1700° to 3500°F. , a pressure in the range of about 1 to 300 atmospheres, an atomic ratio of oxygen/ carbon in the range of about 0-5 to 1.7> and a weight ratio 10 I^O/fuel in the range of about 0 to 5-0, such as about 0.1 to 3-0;
(6) replacing in said central conduit means or annular passage means said feedstream of principal fuel with a replacement feedstream of stand-by fuel by phasing out of the fluid passage means in which it is flowing said stream of principal fuel comprising first solid carbonaceous fuel slurry or hydrocarbonaceous fuel, said phasing out being with a uniformly decreasing rate of flow that varies from maximum to 0 over a period of time in the range of 20 about 1-3600 seconds; and simultaneously phasing said stream of stand-by fuel comprising second solid carbonaceous fuel slurry or hydrocarbonaceous fuel into the same fluid passage means at a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time and mixing with the remaining portion of and replacing the phased out portion of said stream of first solid carbonaceous fuel slurry or hydrocarbonaceous fuel; and simultaneously with or after the completion of said replacement of feedstreams; and simultaneously with or following C6);
* 2 00JS"'
(.7) adjusting the flow rate of the feedstream of free-oxygen containing gas passing through the burner, and . if necessary introducing supplemental H^O into the reaction zone so as to adjust the free oxygen/carbon atomic ratio and the weight ratio I^O/fuel in the reaction zone at design conditions partial oxidation reaction.
By means of the subject process the temperature in the reaction zone may be maintained substantially constant i.e. a variation of less than - 100°F., and the 10 weight ratio ^O/fuel may be maintained in the range of about 0.1 to 3-0.
In the subject flow control means a manual or automatically controlled flow recorder-controller with transmitter is employed to provide signals to a flow rate controller located in each feed line. For slurry fuel feed lines, a signal from the flow recorder-controller is provided to a speed control for a positive displacement pump. For liquid or gaseous hydrocarbon fuel feed lines and for oxidant feed lines, the signal from the flow 20 recorder-controller is provided to a flow control valve. Responsive to said signal(s), the speed of said pump(s) is varied, or alternatively the opening in said flow control valve(s) is changed. By this means, the flow rate for each stream of fuel passing through the burner may be adjusted up or down depending on whether it is being phased in or out.
The velocity of the reactant stream through the central conduit means or annular passage means is In the range of about 0.5-100, such as 10-50 feet per second, 30 say 2-20 ft. per sec. at the face of the burner when said
-a.
2 0.0/59
reactant stream is a liquid hydrocarbon fuel or liquid slurry of solid carbonaceous fuel, or mixtures thereof, and in the range of about 85 feet per second to s.onic velocity, say 100-600 feet per second when said reactant stream is a gaseous hydrocarbon fuel or a free-oxygen containing gas with or without admixture with a temperature moderator or a temperature moderating gas. The velocity of a stream of reactant fuel or a stream of a mixture of reactant fuels exceeds the flame propagation velocity for that fuel or 10 fuel mixture.
The term solid carbonaceous fuels, as used herein to describe suitable solid carbonaceous feedstocks, is intended to include various materials and mixtures thereof from the group consisting of coal, coke from coal, char from coal, coal liquefaction residues, petroleum coke, particulate carbon soot, and solids derived from oil shale, tar sands, and pitch. All types of coal may be used including anthracite, bituminous, sub-bituminous, and lignite. The particulate carbon may be that which is obtained as a 20 by-product of the subject partial oxidation process, or that which is obtained by burning fossil fuels. The term solid carbonaceous fuel also includes by definition bits of garbage, dewatered sanitary sewage sludge, and semi-solid organic materials such as asphalt, rubber and rubber-like materials including rubber automobile tires which may be ground or pulverized to the proper particle size. Any suitable grinding system may be used to convert the solid carbonaceous fuels or mixtures thereof to the proper size.
The solid carbonaceous fuels are preferably 30 ground to a particle size so that 100# of the material passes through an ASTM E 11-70. Sieve Designation Standard
-n-
• 200759
1.4 mm {.Alternative No. 14) -and at least 80$ passes through an ASTM E 11-70 Sieve Designation Standard 425 wm (Alternative No. 40).
The moisture content of the solid carbonaceous fuel particles is in the range of about 0 to 40 wt. %3 such as 2 to 20 wt. %.
The term liquid carrier, as used herein as the suspending medium to produce pumpable slurries of solid carbonaceous fuels is intended to include various materials 10 from the group consisting of water, liquid hydrocarbonaceous material, and mixtures thereof. However, water is the preferred carrier for the particles of solid carbonaceous fuel. In one embodiment, the liquid carrier is liquid carbon dioxide. In such case, the liquid slurry may comprise 40-70 wt. % of solid carbonaceous fuel and the remainder is liquid C02. The C02-solid fuel slurry may be introduced into the burner at a* temperature in the range of about -67°F to 100°P depending on the pressure.
The term liquid hydrocarbonaceous material as used 20 herein to describe suitable liquid carriers and fuels is intended to include various liquid hydrocarbon materials, : such as those selected from the group consisting of liquefied petroleum gas, petroleum distillates and residues, gasoline, naphtha, kerosine, crude petroleum, asphalt, gas oil, residual oil, tar sand oil and shale oil, coal derived oil, aromatic hydrocarbons (such as benzene, toluene,
xylene fractions), coal tar, cycle gas oil from fluid-catalytic-cracking operation, furfural extract of coker gas oil and mixtures thereof.
' - 2 JrJLiv34
■ -- . IS
The term liquid hydrocarbonaceous material as used herein to describe suitable liquid fuels is also intended to include various oxygen containing liquid hydrocarbonaceous organic materials, such as those selected from the group consisting of carbohydrates, cellulosic materials, aldehydes, organic acids, alcohols, ketones, oxygenated fuel oil, waste liquids and by-products from chemical processes for producing oxygenated hydrocarbonaceous organic materials, and mixtures thereof.
For example in one embodiment, the feedstream comprises a slurry of liquid hydrocarbonaceous material and solid carbonaceous fuel. H20 in liquid phase may be mixed with the liquid hydrocarbonaceous carrier, for example as an emulsion. A portion of the H20 i.e., about 0 to 25 weight % of the total amount of H20 present may be introduced as steam in admixture with the free-oxygen containing gas. The weight ratio of H20/fuel may be in the range of about 0 to 5, say about 0.1 to 3»
The term gaseous hydrocarbonaceous material as 20 used herein to describe suitable gaseous hydrocarbonaceous fuels is intended to include a gaseous feedstock from the group consisting of ethane, propane, butane, pentane,
methane, natural gas, coke-oven gas, refinery gas,
acetylene tail gas, ethylene off-gas, and mixtures thereof.
Simultaneously with the fuel stream(s), a free-oxygen containing gas stream is supplied by way of a free passage(s) in the burner. The free-oxygen containing gas may be passed through the central and/or annular conduits at a temperature in.the range of about ambient to 1500°F. ,
. 2 C 0 7 5 9
and preferably in the range of about ambient to 300°F., for oxygen-enriched air, and about 500° to 1200°F., for air, and a pressure in the range of above about 1 to 300 atmospheres, such as 5 to 250 atmospheres, say 10 to 100 atmospheres. The atoms of free-oxygen plus atoms of organically combined oxygen in the solid carbonaceous fuel per atom of carbon in the solid carbonaceous fuel (0/C atomic ratio) may be in the range of 0-5 to 1.95. With free-oxygen containing gas in the reaction zone the broad range of 10 said 0/C atomic ratio may be about 0.5 to 1.7, such as about
0.7 to 1.4. More specifically, with air feed to the reaction zone, said 0/C atomic ratio may be about 0.7 to 1.6, such as about 0.9 to 1.4.
The term free-oxygen containing gas, as used herein is intended to include air, oxygen-enriched air,
1.e., greater than 21 mole % oxygen, and substantially pure oxygen, i.e., greater than 95 mole % oxygen, (the remainder comprising and rare gases).
The free-oxygen containing gas may be supplied 20 with or without mixture with a temperature moderating gas. The term temperature moderator or temperature moderating gas as employed herein is intended to include by definition a member of the group consisting of H20, C02, N2, a recycle portion of the cooled and cleaned effluent gas stream from the gas generator, and mixtures thereof. When supplemental steam is employed as a temperature moderator, all of the steam may be passed through one passageway. Alternatively, about 0 to 25 volume percent of the steam may be mixed with the stream of free-oxygen containing gas and passed 30 through one passageway, and the remainder of the steam may be passed through the remaining passageway.
7C0759
The subject single and multi-annulus pre-mix burners may be operated with the feedstreams passing through alternate passages in the burner. Typical modes of operation are summarized in Tables I to III below.
Table I lists the materials being introduced into the gasifier by way of the burner and their corresponding symbol. The solid carbonaceous fuel (B), water (C)3 and liquid hydrocarbonaceous material (E) may be mixed together in various combinations upstream from the burner inlet to 10 produce a pumpable slurry which may be introduced into the burner and then passed through one of the several free-flow passages of the burner as shown in Table II for the single annulus pre-mix burner (see Figures 1 and 2); and as shown in Table III for the double annulus pre-mix burner (see Figure 3). For examples the first entry in Table II shows that a pumpable slurry stream comprising solid carbonaceous fuel (B) in admixture with water (C) may be passed through the retracted central conduit 15 of a single annulus pre-mix burner i.e. Fig. 1 and 2 while simultaneously a stream of 20 free-oxygen containing gas may be passed through annular passage 17-
Other modes of operation of the subject invention are possible in addition to those shown in Tables II and III.
With respect to the operation of a double annulus embodiment of the burner shown in Fig. 3a the second entry of Table III shows that free-oxygen containing gas (A)
may be passed through both annular passages. In such case, any member of the following group may be simultaneously 30 passed through one or both annular passages 17 and 51:
-<2.1-
air, oxygen-enriched air, and substantially pure oxygen.
Also3 as shown in the seventh entry in Table III, free-oxygen containing gas (A) in admixture with steam (D)_ (say up to 25 vol. % of the total amount of ^0) may be passed through the central conduit 15 and the remainder of the 1^0 as water (C) may be passed through the intermediate annulus 17 as part of the liquid carrier for the slurry.
When the liquid carrier for the slurry of solid carbonaceous fuel is a liquid hydrocarbonaceous material 10 premature combustion within the burner may be avoided by one or more of the following:
(1) keeping the fuel below its autoignition temperature,
(2) including water in the solid fuel slurry,
(3) using air or air enriched with oxygen i.e. up to about 40 vol. % 02,
(4) mixing steam with the air,
(5) employing a double annulus pre-mix burner (Fig. 3) in which the tip of the intermediate exit nozzle has about 0 retraction from the face of the burner. In such
case, the free-oxygen containing gas such as substan tially pure oxygen may be separately passed through the outer annular passage of the burner and into the reaction zone of the gas generator where it reacts by partial oxidation with the multiphase mixture discharged from the pre-mix zone of the burner, and
(6) discharging the multiphase mixture at the exit orifice at the tip of the burner with a discharge velocity which is greater than the flame propagation velocity.
- 3LX
TABLE I
Material
Free-Oxygen Containing Gas Solid Carbonaceous Fuel Water Steam
Liquid Hydrocarbonaceous Material Temperature Moderating Gas
? 0 0 7 5 9
Symbol
A B C D E F
TABLE II
SINGLE ANNULUS PRE-MIX BURNER (See Figures 1 and 2)
Central Conduit Means 15
Annular Passage Means 17
B B B A A A
C C C
+ E
+ D
A A A B B B
D C C E
+ E
TABLE III
DOUBLE ANNULUS PRE-MIX BURNER (See Figure 3)
Intermediate Central Conduit 15 Annulus 17
40
Outer Annulus 51
A
B
+
C
A
B
+
C
A
A
B
+
C
A
F
A
B
+
C
+
E
A
A
B
+
c
+
E
A
+
D
D
B
+
c
+
E
A
A
+
D
B
+
c
+
E
A
B
+
C
+
E
A
A
B
+
C
+
E
D
A
B
+
C
+
E
A
D
A
B
+
E
A
+
D
A
+
D
B
+
E
A
A
+
D
B
+
E
A
+
D
D
B
+
E
A
A
B
+
E
D
B
+
E
A
+
D
A
+
D
B
+
E
A
A
+
D
B
+
E
D
A
B
+
E
A
D
A
B
+
E
F
F
B
+
C
A
A
B
+
C
F
E
B
+
c
A
B
+
C
E
A
200759
The subject burner .assembly is inserted downward through a top inlet port of a compact unpacked free-flow noncatalytic refractory lined synthesis gas generator, for example as shown in Figure 1. The burner extends along the central longitudinal axis of the gas generator with the downstream end discharging a multiphase mixture of fuel, free-oxygen containing gas, and temperature moderator directly into the reaction zone.
The relative proportions of solid or solid and
liquid fuel, water and oxygen in the feedstream to the gas generator are carefully regulated to convert a substantial portion of the carbon in the fuel e.g., up to about 90% or more by weight, to carbon oxides; and to maintain an autogenous reaction zone temperature in the range of about 1700° to 3500°F., preferably in the range of 2000 to 2800°F.
The dwell time in the reaction zone is in the range of about 1 to 10 seconds, and preferably in the range of about 2 to 8. With substantially pure oxygen feed to the gas generator, the composition of the effluent gas from the
gas generator in mole % dry basis may be as follows: H2 10 ^ L 8. gf a
,, * to 60, CO 20 to 60, CO, 5 to 40, CH. 0.01 to 5, H9S+COS 0 to fv c^p-/Q 5, N2 nil to 5, and ^ nil to 1.5. With air feed to the gas generator, the composition of the generator effluent gas in mole % dry basis may be about as follows: H2 2 to 20, CO 5
pip
A. to 35, C02 5 to 25, CH4 0 to 2, H2s+C0S 0 to 3, N, 45 to 80, P*r ffr- flr
IQ /plj to I'S- Unconverted carbon and ash are contained in the effluent gas stream.
2 0yV ^
The hot gaseous effluent stream from the reaction zone of the synthesis gas generator Is quickly cooled below the reaction temperature to a temperature in the range of about 250° to 700°F. by direct quenching in water, or by indirect heat exchange for example with water to produce steam in a gas cooler. The gas stream may be cleaned and purified by conventional methods.
A more complete understanding of the invention may be had by reference to the accompanying schematic drawing which shows the subject invention in detail. Although the drawing illustrates preferred embodiments of the invention, it is not intended to limit the subject invention to the particular apparatus or materials described.
Referring to the figures in the drawing, FIG. 1 is a schematic representation of one embodiment of the invention showing control means for the continuous operation of a synthesis gas generator while phasing out one fuel and simultaneously phasing in another without depressurizing the gas generator. Further, the control means may be used for rapidly changing throughput levels - up or down over the flow range for which the burner shown is designed. By this means adjustments may be made to control the amount of raw effluent gas produced, and to provide for a change in demand for the pr-oduct gas. Further, another use for the control system is to maintain the desired composition of the product gas when possible to do so by adjustments to the flow rates of one or more of the reactant streams. Thus, by the subject flow control system, the flow rates for all of the reactant streams are separately and
200/5
Independently controlled so that the temperature and weight ratio of to fuel in the reaction zone are maintained at design conditions and within desired operating ranges for the fuel being reacted. If necessary the atomic ratio of free-oxygen to carbon in the fuel in the reaction zone may also be controlled within design conditions.
While the control system shown in Figure 1 is specifically designed for the combination of feedstocks comprising a solid carbonaceous fuel slurry and a liquid 10 hydrocarbonaceous fuel, by simple modifications to the means for changing the flow rate of the fuel stream as described below, the system may be used to control other combinations of solid carbonaceous fuel slurries, and liquid, or gaseous hydrocarbonaceous fuels.
In Figure 1, burner 1 is mounted in central flanged inlet 30 which is located in the upper head of conventional refractory lined free-flow synthesis gas generator 41 along the central longitudinal axis. The reactant streams enter through the upstream end of burner 1 20 pass downward therethrough, and are discharged through downstream end 42. Burner 1 is designed so that the required system output for steady-state operation may be achieved or even exceeded by a specified amount when the flow rate through all passages Is a maximum. The control system can independently change the flow rate of any one or more of the feedstreams in lines 181, l6l, 43 and 63-By this means the temperature In the reaction zone 31 Is
-at -
200759
maintained at the desired operating temperature. Further, the weight ratio E^O to fuel, and if necessary the atomic ratio of free-oxygen to carbon in the fuel in the reaction zone may be maintained at design conditions.
Operation of the process and control system shown in Figure 1 follows. For purposes of illustration, the principal fuel may be for example a solid carbonaceous fuel slurry i.e. coal-water or coal-oil slurry In line 43* The stand-by fuel Is a liquid hydrocarbonaceous fuel 10 i.e. residual oil in line 161. Of course, the principal fuel may have been chosen to be any liquid or gaseous hydrocarbonaceous fuel.
In the subject process, the remaining portions of the principal fuel stream being phased out of line 50 is mixed in line 14 with the stand-by fuel stream being phased into line 167■ E^O may be in admixture with the fuels in lines l6l and 43 or the free-oxygen containing gas in line 63. Alternatively, as shown in Fig. 1, at least • a portion i.e. 10-100 vol. % of the 1^0 may be provided 20 as the temperature moderator, for example steam. Thus, as shown in Fig. 1, steam in line 187 preferably may be mixed in line 18 with the free-oxygen containing gas flowing in line 70. By this scheme, controlled amounts of steam may be introduced into and mixed with the stream of free-oxygen containing gas and/or fuel upstream from the burner.
Valves 183, 163, 77, and 65 may be manually or
t ■■■■ i 1 Q
//.. %.') '-w / -
• _
automatically operated to obtain a wide open position to a completely closed position. The rates that each valve may be opened and closed is also controllable. The slurry feedstream in line 43 is pumped into the reaction zone 31 of synthesis gas generator 41 by way of positive displacement pump 45 equipped with speed control 46, line 47, flow measurer and transmitter .48, line 49, valve 77, lines 50 and 14, and inlet 8 of burner 1. The slurry flow rate through line 43 is controlled by the speed of positive 10 displacement pump 45. In order to phase out the slurry flowing through line 43, this speed is continuously decreased from maximum to zero over a period in the range of about 1 to 3600 seconds, such as about 60 to 1800 seconds, say about 300 to 1000 seconds. Flow recorder-controller with transmitter 51 includes a microcomputer means which is programmed with the desired time vs. decreasing flow rate curve. The rate of slurry flow in line 47 is measured and a signal a is provided by flow transmitter 48 corresponding to the flow rate of the slurry In line 43. Flow recorder-20 controller 51 receives signal a, compares it with a signal representing the desired flow rate for that moment, and provides a corresponding adjustment signal to speed control 46 to adjust the speed of pump 45 downward so that the charge slurry flowing in line 49 assumes a given decreased flow rate for that moment in the phase-out period. The
"24*
p- L- B. & A. /py
200759
new slurry rate is measured and the cycle is repeated. By this means, repeated adjustments to the rate of flow are made and the slurry flowing in line 50 is phased out.
Simultaneously with the phasing out of the principal slurry fuel flowing in line 43, the stand-by liquid hydrocarbonaceous fuel flowing in line 161 is phased in over the same period of time. Flow recorder-controller with transmitter 171 includes a microcomputer means which is programmed with the desired time vs. increasing flow rate 10 curve. The rate of oil flow in line 161 is measured and a signal m is provided by flow transmitter 165 corresponding to the flow rate of the oil in line 161. Flow recorder-controller 171 receives signal m, compares it with a signal representing the desired flow rate for that moment and n provides a corresponding adjustment signal to valve 163 to
P«r~JXZL lfc>*7
open wider so that the charge oil in line 3r6-6 assumes a given increased flow rate for that moment in the phase-in period. The new oil rate is measured and the cycle is repeated. By this means, repeated adjustments to the rates 20 of flow of the principal and stand-by fuels may be made so that the oil flowing in line 167 may be phased into line 14 in an amount that compensates for the reduced amount of solid carbonaceous fuel slurry flowing in line 50.
During or following the period that the portion of principal solid carbonaceous slurry fuel from line 4 3 is phased out and the portion of stand-by liquid hydrocarbon fuel from line 161 is phased in, the weight ratio of I^O to fuel in the reaction zone may be controlled at design conditions or maintained substantially constant i.e. less 30 than +10% variation, by increasing or decreasing the flow rate of the temperature moderator. AccordinglyATu>.7,
0.^ v -2JL*;J934
2 0 07 5
in the subject example, simultaneously with the phase-out of the coal-water slurry a supplemental amount of H20 from an external source may be phased in over the same period of time. Thus, in Fig. 1, a portion of the steam in line 181 is passed through line 187 and phased into line 18 where it mixes with the free-oxygen containing gas from line 70. Flow recorder-controller with transmitter 191 includes a microcomputer means which is programmed with the desired time vs. increasing flow rate curve.
The rate of steam flow in line 181 is measured and a signal s is provided by flow transmitter 185 corresponding to the flow rate of the steam in line 181. Flow recorder-controller 191 receives signal s, compares it with a signal representing the desired flow rate for that moment and provides a corresponding adjustment signal to valve 183 to open wider so that the charge steam in line 186 assumes a given increased flow rate for that moment in the phase-in period. The new steam rate is measured and the cycle is repeated. By this means, repeated adjustments to the rate 20 of steam flow are made and the steam flowing in line 187 is phased into line 18 in an amount that will maintain the weight ratio of H20 to fuel in the reaction zone at design conditions, for example substantially constant. In smother embodiment the weight ratio I^O/fuel in the reaction zone is adjusted up or down by controlling the steam rate as described previously in order to obtain a desired temperature in the reaction zone and composition of the product gas.
Simultaneously with or after the phasing out of the principal fuel, the phasing in of the stand-by fuel, and 30 optionaly with or without the phasing in or out of the steam depending on the nature of the fuels, the free-oxygen
~3>o ^
containing gas may be adjusted up or down. By this means the temperature in the reaction zone may be controlled at design conditions, or maintained substantially constant i.e. less than +200°F. variation. Thus, in the present example in Fig. 1, a portion of the free-oxygen containing gas in line 63 is passed through line 70 and phased into line 18 where it mixes with the .steam, if any, from line 187 as previously described. Flow controller 74 is programmed with the desired time vs. flow rate curve. The period of adjustment is the same as that for the fuel and steam streams. The adjustment to the oxygen flow rate may be up or down depending on the nature of the fuel streams and the addition of steam, if any. In the subject-example, the oxygen flow rate will be increased to satisfy the additional requirements for the partial oxidation of a liquid hydrocarbon in comparison with a solid carbonaceous fuel.
The rate of free-oxygen containing gas in line 63 is measured and a signal b is provided by flow transmitter 67 corresponding to the flow rate of the free-oxygen containing gas in line 63. Flow recorder-controller with transmitter 74 includes a microcomputer means which receives signal b, compares it with a signal representing the desired flow rate for that moment, and provides a corresponding adjustment signal to valve 65 to open wider so that the charge free-oxygen containing gas in line 68 assumes a given increased flow rate for that moment in the phase-in period. The new free-oxygen containing gas rate is measured and the cycle is repeated. By this means repeated adjustments to the rate of oxygen flow are made and the free-oxygen containing gas flowing in line 70 is phased into line 18 in an amount that
2.00759
i J
will maintain the temperature in the reaction zone at design conditions or substantially constant. In ontb embodiment in which the burner shown in Figure 3 is employed, a portion of the temperature moderator, for example steam in line 187, is passed through inlet 13 of the burner.
In another embodiment, the free-oxygen containing gas rate is adjusted up or down to obtain a desired temperature in the reaction zone and composition of the product gas. Alternatively, by the previously described means, the atomic 10 ratio of oxygen to carbon in the reaction zone may be controlled at design conditions i.e. in the range of about 0.5 to 1.7.
The previously mentioned time vs. flow rate curves for programming conventional flow recorder-controllers 191, 171, 51, and 74 may be determined by conventional calculations based on heat and weight balances for the entire system.
In another embodiment, the parameters for said calculations and any others may be measured by conventional detectors and the signals responsive thereto may be fed to 20 an overall control system means 40. The input to system control means 40 may be manual or a signal from a computer, analyzer, or sensor. Control means 40 comprises conventional circuits and components for providing or converting signals i.e. pneumatic or electronic to operate said speed controls and valves.
-3>v
In control means 40, the computer calculated values or the manually inserted set points for the desired rates of flow at specific moments for the various streams are compared respectively with the signals a, m, s and b. For example, responsive to signal a, control means 40 may automatically control pump speed control 46 by sending signal c to flow-recorder-controller 51. Alternatively,
signal c may be fed directly to speed control 46. In another embodiment, for example flow recorder-controller 51 may 10 receive signal a from flow transmitter 48 and signal c from control means 40 and compute the speed adjustment signal for the operation of speed control 46. In still another embodiment, the flow of the feedstream may be stopped by a signal i from control means 40 to valve 77.
Similarly, responsive to signal m, control means 40 may automatically control liquid hydrocarbonaceous fuel valve 163 by sending signal w to flow-recorder-controller 171.
In a similar manner, responsive to signal s, 20 control means 40 may automatically control steam valve 183 by sending signal u to flow-recorder-controller 191.
Also, similarly, responsive to signal b, control means 40 may automatically control free-oxygen containing gas valve 65 by sending signal j to flow-recorder-controller 74.
Two suitable burners for use in the subject
<S
process and control system are shown in Figures 1-3-Corresponding parts of the burner shown in Figures 1 and 2 have the same reference number.
Burner 1 is shown in greater detail in Fig. 2 and substantially comprises unobstructed inner coaxial retracted central conduit means 15 and outer concentric coaxial conduit 16 which is disposed longitudinally about inner central conduit means 15- Disc flange 10 is attached 10 to the outside circumference of outer coaxial conduit 16
and supports burner 1 In a vertical longitudinal direction. The central longitudinal axes of burner 1 and gasifier 41 are coaxial. Spacing means 18 provide a free-flow annular passage means 17 between the outside diameter of central cylindrical conduit means 15 and the inside diameter of outer cylindrical conduit 16. Exit orifice 20 at the downstream tip of central conduit 15, is preferably straight, circular in cross-section, and perpendicular to the longitudinal axis of the burner. Alternatively, exit 20 orifice 20 may be converging or diverging. Outer conduit 16 terminates at the downstream end of the burner with converging nozzle 21. A vertical cross-section of exit orifice 21 may be frusto-conically shaped, which may or may not merge into a right cylinder. Preferably for wear resistance, as shown in Fig. 2, nozzle 21 comprises a frusto-conical rear portion 22 that develops Into a right cylindrical front portion 23 which terminates at the downstream face 6 of the burner. The cylindrical exit section will permit: (1) additional burner life because of
\
200759
increased surface available for abrasion, and (_2) fabrication of a ceramic or refractory insert or an entire cooling chamber from a thermal and abrasion resistant material i.e., tungsten or silicon carbide in order to reduce damage and to extend burner life.
The height of the front cylindrical portion 23 of exit nozzle 21 is in the range of about 0 to 1.5j say about 0.1 to 1.0 times, its own diameter i.e. the minimum diameter of converging nozzle 21. The diameter of exit orifice 20 of 10 central conduit 15 is in the range of about 0-2 to 1-5, say about 0.5 to 0.8 times the minimum diameter of converging nozzle 21.
The downstream end of the burner may or may not be cooled. Preferably, as shown in Fig. 2, coaxial annular shaped cooling chamber 2 surrounds exit orifice 21 at the burner tip. By passing water through cored section 24 of cooling chamber 2, the tip of burner 1 may be prevented from overheating. Optionally for similar reasons, outer conduit 16 may be kept cool by passing water through coils 4 which 20 encircle the outside surface of outer conduit 16 along its length. Suitable converging angles for orifice 21 are in the range from about 15° to 90° from the central longitudinal axis of the burner. The downstream tip of exit orifice 20 of central conduit means 15 is severely retracted upstream from face 6 of burner 1 a distance of two or more times the minimum diameter of converging exit nozzle 21. For example, the setback of tip 20 of central conduit 15 from burner face 6 may be in the range of about 3 to 10 times the minimum diameter of converging exit nozzle 21. The space between
^ /T\
tip 20 of central conduit 15 and burner face 6 constitutes the unobstructed pre-mix £one.
In the operation of burner 1, either reactant stream i.e. see Table II supra, may enter burner 1 by way of inlet 9 of Fig. 1 and pass directly from the upstream portion down through free-flow central conduit 15, through exit orifice 20, and into pre-mix zone 25, as shown in Fig. 2. Cover plate 11 seals off the upper end of annular passage means 17• The upstream inlet end 9 of central conduit 15 is coupled to a feed line and the downstream end passes through cover plate 11 and is sealed thereto. Simultaneously, the other reactant stream may enter burner 1 by way of inlet 8 and pass directly from the upstream portion 30 of outer conduit 16 down through free-flow annular passage 17 and into pre-mix zone 25 where intimate mixing of the two reactant streams takes place. Inlet 8 may or may not be tangential to outer conduit 16. Further, direct heat exchange between the two reactant streams takes place in pre-mix zone 25. The temperature in the pre-mix zone is controlled so that a controlled amount of the liquid carrier may be vaporized without burning i.e. from 0 to 100 vol. % say about 2 to 80 vol. %. Temperature control in the pre-mix zone may be effected by controlling such factors as dwell time and heat content of the entering streams, and amount of external cooling such as by coils 4, if any. Pre-mix zone 25 is substantially free from any obstruction to the free-flow of the materials passing therethrough.
In the burner shown in Figs. 1 and 2, streams of different materials flowing down through coaxial retracted central conduit 15 and simultaneously down through annular passage 17 are successively mixed together in tandem pre-mix chambers 25 and 40'. While the pre-mix zone in this embodiment is shown as comprising two separate coaxial pre-mix chambers 25 and 40' in series, the pre-mix zone for other embodiments of the subject invention may actually comprise one or more,
such as 2 to 5 coaxial pre-mix chambers. For example, three pre-mix chambers 25, 40', and 41 are included in the embodiment of the burner shown in Fig. 3. Each pre-mix chamber in Figures 1, 2 and 3, except for the first chamber in the line, comprises a coaxial cylindrical body portion 45 followed by a coaxial at least partially converging outlet portion 22 or 46 in Fig. 3 that may optionally develop into a straight cylindrical portion 23 or 49, respectively. Optionally,
such outlets may be made from a thermal and wear resistant material i.e. silicon or tungsten carbide, such as previously described. In embodiments having a plurality of pre-mix chambers, the first pre-mix chamber in the line may have a straight coaxial cylindrical body portion 47, that discharges through circular orifice 39 directly into the next in line coaxial pre-mix chamber 40'. Alternatively, one or more of the pre-mix chambers may be a converging frusto-conical shaped section. Preferably, the mixture leaving one pre-mix chamber expands into the next successive pre-mix chamber.
When the mixture is accelerated and expanded through a final exit nozzle at the tip of the burner into the combustion chamber, a more stable and efficient combustion pattern results. The temperature, pressure and velocity ranges for
-"V7 -
P., L. B. & A.
V -200759 ■
the streams of materials passing through the various passages of the burner are substantially, the same as those discussed previously. The inlet to the first pre-mix chamber 25 may have a converging inlet 48 as shown in Figures 1, 2 and 3.
FIG. 3 is a vertical sectional view of an embodiment of the retracted central conduit 15 pre-mix burner similar to burner 1, as shown in Fig. 2, but modified to provide two coaxial annular passages i.e. intermediate annular passage 17 and outer annular passage 51. Further, the pre-mix zone comprises three successive free-flow coaxial pre-mix chambers 25, 40', and 41. By spacing means 18, concentric coaxial outer conduit'52, retracted coaxial intermediate conduit 53, and retracted coaxial central conduit 15 may be radially spaced from each other to provide said separate annular passages and pre-mix chambers with substantially no obstruction to the free-flow of materials therethrough. The downstream tip 20 of central conduit 15 is retracted upstream from face 6 of the burner a distance in the range of 2 or more, say 3 to 10 times the minimum diameter of converging exit orifice 21.- The downstream tip 54 of intermediate conduit 53 is retracted upstream from face 6 of the burner a distance in the range of 0 to 12, say 1 to 5 times the minimum diameter of converging exit orifice 21.
Central conduit 15, and annular passages 17 and 51 of the burner in Fig. 3 are respectively connected upstream to separate inlets in a manner similar to that shown in Fig.
per.
I C> IT"1 T^us' t^le upstream inlet end f of inlet pipe 9 of fIZ.lrATiZAT
2 JUL -934
*?;
7 5
central conduit 15 is coupled to a feed line and the downstream end passes through cover plate 12 and is sealed thereto. Cover plate 12 seals off the upper ends of annular passages 51 and 17. Simultaneously, the other feedstreams may enter burner 1 by way of upstream inlet 8 that leads into annular passage 17, and upstream inlet 13 which leads into annular passage 51. Optionally, annular disc 56, with or without a plurality of small diameter holes 57, may close off the downstream end of annular passage 51. Inlets 8 and 13 may or may not be tangential to coaxial intermediate conduit 53 and outer conduit 52, respectively. The burner tip may be cooled by passing water through cored section 24 of annular cooling chamber 2 which is coaxial with the central longitudinal axis of the burner at the downstream end in the manner shown. Alternatively, cooling chamber 2 may be eliminated. Cooling coils 4 may encircle the burner along its length.
In the operation of the embodiment of the burner shown in Figure 3, the feedstreams simultaneously passing down through central conduit 15 and intermediate annular passage 17 at different velocities impinge and mix with each other in the first pre-mix chamber 25. The impingement of one reactant stream, such as the liquid slurry of solid carbonaceous fuel in a liquid medium with another reactant stream, such as a gaseous stream of free-oxygen containing gas, steam, or temperature moderator at a higher velocity causes the liquid slurry to break up into a fine spray. The multiphase mixture then passes into the second pre-mix chamber 40' for additional mixing. Leaving chamber 40' by way of converging exit nozzle 46 and circular orifice 54 at
'7>ci-
the downstream tip of chamber 4 0', the multiphase mixture passes into the third pre-mix chamber 41. The third feed-stream enters the burner upstream through a separate inlet 13, and passes down outer annular passage 51. Optionally, at least a portion of the third feedstream in annular passage 51 may be mixed with the other feedstreams in annular passage 17 and pre-mix chamber 25, 40', and 41 by being passed through a plurality of rings of small diameter passages or holes 60, 61, 62 and 57 located in the wall of intermediate conduit 53 and annular disc 56. When the set back of orifice 54 at the tip of intermediate conduit 53 from face 6 of the burner is greater than 0, say in the range of about 1.0 to 5 times the minimum diameter of exit orifice 21, then the third feedstream may mix with the first and second feed-streams in pre-mix chamber 41 to produce a multiphase mixture. Further, in such embodiment, there may be 2 or more say 2 to 5 cylindrical coaxial pre-mix chambers in series. The multiphase mixture passes through converging nozzle 21 at the downstream tip of the burner into the reaction zone of the gas generator.
In the embodiment of the burner shown in Fig. 3
t with a set back of orifice 54 of about 0, the third feedstream passing through outer annular passage 51 will contact and mix with the multiphase mixture of the other two feedstreams from the pre-mix zone downstream from face 6 of the burner, say about 1 to 2 4 inches. Further, in such embodiment,
there may be one or more say 2 to 5 cylindrical coaxial pre-mix chambers in series. For example, the stream of free-oxygen containing gas may be passed through either central conduit 15 or intermediate passage 17 and the fuel feedstream may be passed through the other passage i.e. the central
200759
conduit or intermediate passage whichever is free. Simultaneously, a stream of temperature moderator may be passed through the outer annulus passage 51.
Reference will now be made to Figures 4 and 5 of the generator, it may be necessary to rapidly turndown the production of the effluent gas to about 1/8 to 3/4 of the plant-design output, without replacing the burner. Changing the burner requires a costly shut-down period with resultant 10 delay. Thus, in combined cycle operation for power generation a durable burner is required which offers minimum pressure drop and with which throughput levels may be rapidly changed - up and down - without sacrificing stable operation and efficiency. Further, the burner should 15 operate with a variety of liquid, solid, and gaseous fuels, and mixtures thereof. Combustion instability and poor efficiency can be encountered when prior art burners are
drawings. During operation of the partial oxidation gas
2 00 7
used for the gasification of liquid phase slurries of solid carbonaceous fuels. Further, feedstreams may be poorly mixed and solid fuel particles may pass through the gasifier without contacting significant amounts of oxygen. Unreacted oxygen in the reaction zone may then react with the product gas.
These problems and others are avoided by a novel two-section burner employed in the subject process comprising: a central conduit, said central conduit being 10 closed at the upstream end and having a downstream circular exit orifice at the tip of the burner; an outer conduit coaxial and concentric with said central conduit and forming an annular passage therebetween, said outer conduit and annular passage being closed at the upstream end and having a downstream annular exit orifice at the tip of the burner; a central bundle of open-ended parallel or helical tubes passing through the closed end of said central conduit and making a gas tight seal therewith; means for supporting said central bundle of parallel or helical tubes so that the 20 external surfaces of said central bundle of parallel or helical tubes forms a plurality of passages within said central conduit; upstream inlet means including a manifold for splitting and introducing a first reactant feedstream into the upstream ends of said central bundle of parallel or helical tubes; and wherein the downstream ends through which said first feedstream is discharged are retracted upstream from the burner face a distance of 0 to 12 say about 3 to 10 times the minimum diameter of the central conduit exit orifice at the tip of the burner; upstream 30 inlet means for introducing a second reactant feedstream
-o) f- /• c '>/ fr0 /V •>
into said central conduit and dovm through said plurality of passages within said central conduit; an annular bundle of open-ended parallel or helical tubes passing through the closed end of said annular passage and making a gas tight seal therewith, so that the external surfaces of said annular bundle of parallel or helical tubes forms a plurality of „ passages within said annular passage; upstream inlet means including a manifold for splitting and introducing a third reactant feedstream into the upstream ends of said annular 10 bundle of parallel or helical tubes, and wherein the downstream tube ends through which said third rsactant feedstream is discharged are retracted upstream from the burner face a distance of 0 to 12 say about 3 to 10 times the minimum width of the annular exit nozzle at the tip of the burner;
means for supporting said annular bundle of parallel or helical tubes with respect to the inside wall of said annular passage and to each other so that the external surfaces of said annular bundle of parallel or helical tubes forms a plurality of passages within said annular passage; and upstream inlet 20 means for introducing a fourth reactant feedstream into said annular passage and down through said plurality of passages within said annular passage.
Advantageously, by means of the subject burner,
three ranges of flow through the burner may be obtained by using one or both bunches of tubes and their surrounding conduits. Throughput levels may be rapidly changed -up and down - without sacrificing stable operation.
In one embodiment of the aforesaid burner in which the downstream ends of the central and/or annular 30 bundles of parallel or helical tubes are retracted upstream
007 59
from the burner face, additional mixing of the feedstreams may be obtained by providing at least one coaxial cylindrical shaped pre-mix chambers in series in said central conduit in which said first and second feedstreams are mixed, and/or at least one coaxial annular shaped pre-mix chambers in series in said annular passage in which said third and fourth feedstreams are mixed.
longitudinal gas conduits parallel to the burner axis and 10 radially spaced between said central conduit and said annular passage. Said gas conduits are closed at the downstream end near the burner tip and are connected to a gaseous feedstream at the upstream end. A plurality of feeder lines connect said gas conduits to said pre-mix chambers in said central conduit and/or to said annular passage. A gaseous feedstream selected from the group consisting of steam, free-oxygen containing gas, CO^, N , fuel gas, a recycle portion of the product gas, and mixtures thereof may be thereby passed through said 20 longitudinal gas conduit and feeder lines and into said pre-mix chambers to improve mixing, break-up packed passages, or to introduce a gaseous constituent which will influence the reaction going on in the gasifier.
and/or annular bundle(_s)_ of tubes, or alternatively through the conduitC.s)_. surrounding the tubes in the central and/or annular sections of the burner. Simultaneously the free-oxygen containing gas is passed through the corresponding unoccupied passageOI in the central ana/or annular sections 30 of the burner. In one embodiment, one type of fuel is
The burner may be provided with a plurality of
The fuel may be passed through either the central
? 00
7
passed through one section of the burner i.e. central or annular section, while a second type of fuel is passed through the remaining section of the burner.
Preferably, in the subject two-section burner said first and third reactant feedstreams and said second and fourth reactant feedstreams are respectively made up of split streams from the fuel stream(s), and the gaseous oxidant stream. By this means, fuel is passed through the central and annular bundles of tubes, while simultaneously 10 free-oxygen containing gas is passed through the corresponding central and annular conduits. In one embodiment, however, the first and fourth feedstreams, and the second and third feedstreams are respectively made up of split streams from the fuel stream (.s), and the stream of gaseous oxidant. By this means, fuel is passed through the central bundle of tubes and the annular conduit, while simultaneously free-oxygen containing gas is passed through the corresponding central conduit and annular bundle of tubes.
process for controlling the introduction of said reactant feedstreams Into the burner. Further, means are provided for changing fuels without shutting down or depressurizing the gas generator.
tubes or surrounding passages in the central and/or annular sections of the burner, some preferred embodiments of the subject process for replacing the principal fuel with the stand-by fuel follow:
CQ the replacement of the principal fuel with the 30 stand-by fuel may take place simultaneously In the central
Flow control means are provided In the subject
When the principal fuel is flowing through the
'T) ^ // ir v:
'and/or annular sections of the burner.
(2) alternatively3 the replacement of the principal fuel with the stand-by fuel may take place sequentially, and first in either one of the sections of the burner. This is then followed by the substitution of the fuels in the remaining section of the burner.
When a stream of the principal fuel is flowing through only one section of the burner and the other section is unused, then first a stream of the stand-by fuel may be 10 introduced into the unused section of the burner. The principal fuel may be stopped in the section in which it is flowing along with the related stream of free-oxygen containing gas with or without mixture with a temperature moderating gas. The principal fuel stream may be stopped simultaneously with or after the introduction of the stand-by fuel stream. In such case, after the stand-by fuel replaces the principal fuel only one section of the two-section burner is in use. Alternatively, the principal fuel may be also replaced in the section in which it was 20 originally flowing by a stream of said second solid carbonaceous fuel slurry or hydrocarbonaceous fuel. In such case, after the stand-by fuel replaces the principal fuel both sections of the burner are in use.
In the above schemes, the principal and/or stand-by fuels may or may not be in admixture with ^0. Adjustments are made to the free-oxygen containing gas stream with or without mixture with a temperature moderating gas flowing in the tubes or surrounding passages that are related to the corresponding surrounding passages or tubes 30 in which the fuel stream is flowing and if necessary
-Wt-
2 007 59
supplemental H^O is introduced into the reaction zone so as to maintain the weight ratio of the H^O to fuel and the temperature in the reaction zone at design conditions. For example, the temperature in the reaction zone may be maintained substantially constant I.e. less than 1 200°F. variation; and, the weight ratio H^O/fuel in the reaction zone may be maintained in the range of about 0-2-3.0.
Thus, if the principal or first fuel flowing through a first or second fluid passage in the central or
first section of the burner and/or through the third or fourth fluid passage in the annular or second section of the burner becomes unavailable and it is desired to switch to a stand-by or second fuel, or for any reason whatsoever it is desired to switch from a first solid carbonaceous fuel slurry or hydrocarbonaceous fuel to a second solid carbonaceous fuel slurry or hydrocarbonaceous fuel, one may proceed as follows:
/
(1) passing a first reactant stream of first solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with H^O through either the first or second
fluid passage means in the central or first section of said burner, and/or simultaneously passing a second reactant stream of said first solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with H^0 through either the third or fourth fluid passage means in the annular or second section of said burner;
(2) simultaneously passing a separate reactant stream of free-oxygen containing gas with or without mixture with a temperature moderating gas through the unused fluid passage means in each of the central and/or annular sections
of said burner which are related to said fluid passage
t
O fii 7
c' iy l; y *
means through which said stream(s) of first solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with H20 are passing;
(3) mixing together said reactant streams from (1) and (2) to produce a well-distributed blend, and reacting said mixtures by partial oxidation in the reaction zone of said gas generator at an autogenous temperature in the range of about 1700° to 3500°F., a pressure in the range of about 1 to 300 atmospheres, an atomic ratio of oxygen/carbon in the range of about 0.5 to 1.7, and a weight ratio i^O/fuel in the range of. about 0 to 5.0;
(4) phasing out of the fluid passage means in which it is flowing in said central and/or annular section(s) said stream(s) of first solid carbonaceous fuel slurry or hydro-
carbonaceous fuel with or without mixture with B^O, said phasing out being with a uniformly decreasing rate of flow that varies from maximum to 0 over a period of time in the range of about 1 - 3600 seconds; and simultaneously phasing said stream(s) of second solid carbonaceous fuel slurry or 20 hydrocarbonaceous fuel with or without mixture with H20 into the same fluid passage means at a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time and mixing with the remaining portion of and replacing the phased out portion of said stream of first 25 solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with H20 flowing therein, and
(5) controlling the temperature and weight ratio H20/fuel in the reaction zone at design conditions by adjusting the flow rate(s) of the reactant stream(s) of free-oxygen
containing gas with or without mixture with a temperature moderating gas passing through the burner, and if necessary introducing supplemental H20 into the reaction zone.
For example, by means of the subject process the temperature in the reaction zone may be maintained substantially 35 constant i.e. a variation of less than - 200°F., and the weight ratio H20/fuel may be maintained in the range of about 0.2 to 3.0.
? QQ7 59
In the subject flow control means a manual or automatically controlled fluid-controller is placed in each feed line. For slurry fuel feed lines, a signal from the controller is transmitted to a speed control for 5 a positive displacement pump. For liquid or gaseous hydrocarbon fuel feed lines and for oxidant feed lines, the signal from the controller is transmitted to a flow control valve. Responsive to said signal(s), the speed of said pump(s) is varied, or alternatively the opening in said flow control 10 valve(s) is changed. By this means, the flow rate for the streams of fuel and/or oxidant passing through the burner may be
-4^ -
adjusted up or down, say up to about 50% of the Design Conditions. Alternatively, a flow control valve may be inserted in each of the feedstreams to start or stop the flow of the feedstreams to the central conduit and/or the annular passage and to their respective bundles of tubes.
By this means, three ranges of flow through the burner may be obtained. Further, both of these flow control schemes may be combined.
By means of the subject burner a large volume of 10 the first reactant stream is split into a plurality of separate streams of reactant fluid flowing through the central bunch of helical or parallel tubes. This permits the introduction of the second stream of reactants passing concurrently through the central conduit into the interstices and/or passages surrounding the central bunch of helical or parallel tubes. Similarly, a large volume of the third reactant stream is split into a plurality of separate streams of reactant fluid flowing through the annular bunch of helical or parallel tubes. The fourth stream of reactants 20 passing concurrently through the annular passage is introduced into the Interstices and/or passages surrounding the annular bunch of helical or parallel tubes. The greater the number of tubes in a bunch, the better the distribution of one reactant within the other reactant. The mixing of the reactant streams which takes place downstream of the ends of the tubes is facilitated by this improved distribution.
Such efficient mixing of the feedstreams facilitates a more uniform partial oxidation of the fuel to produce ana CO. The combustion efficiency of the process is thus increased. 30 By means of the subject Invention, reactions are made to proceed in local regions where there is less
opportunity for overheating the fuel with an insufficient supply of oxygen to result in the formation of soot. Thus, the amount of unconverted particulate carbon produced for a given oxygen to carbon atomic ratio in the feed may be substantially reduced. Further, "overburning" of the fuel to produce carbon dioxide is substantially reduced. The subject burner Is preferably made from heat and corrosion-resistant metal alloys.
The velocity of the reactant stream through the 10 central and annular bunches of tubes, or alternatively through the central conduit or annular passage surrounding said tubes is in the range of about 5-100, say 10-50 feet per second at the face of the burner when said reactant stream is a liquid hydrocarbon fuel or liquid slurry of solid carbonaceous fuel, or mixtures thereof, and in the range of about 150 feet per second to sonic velocity, say 200-500 feet per second when said reactant stream is a gaseous hydrocarbon fuel or a free-oxygen containing gas with or without admixture with a temperature moderator. 20 The velocity of a stream of reactant fuel or a stream of a mixture of reactant fuels exceeds the flame propagation velocity for that fuel or fuel mixture.
The central bunch of tubes may number in the range of about 1-200 or more, such as about 2-180 say about 4-48. The annular bunch of tubes may number in the range of about 1-600, or more, such as about 2-580, say about 8-108.
There may be 1 to 7' or more concentric rings of tubes in the central and/or annular bundles.
The ratio of the total tube cross-sectional area 30 (basis inside diameter)! for the annular bunch of tubes (T^)
' "to the total tube cross-sectional area (basis inside diamete_r)
for the central bunch of tubes (T ) may be in the range of
C
about 2-8. Similarly, the ratio of the annular interstitial cross-sectional area (1 ) surrounding the annular bunch of
A
tubes to the central interstitial cross-sectional area (I ) surrounding the central bunch of tubes may be in the range of about 2-8.
The inside diameter of the tubes in either bunch may range from about 1/16 to 2 inches in diameter. The 10 length of the tubes in the central and annular bunches and their spacing are such as to permit the external reactant stream to flow evenly into the interstices between the tubes. For example, the length of the tubes or the height of the coils in either tube bundle may range from about 1/2 to 36 inches or longer and preferably from about k to 12 inches, with greater lengths required as the number of tubes and the total size of the burner increases. Preferably, the ratio of the length to inside diameter of the tubes should be at least 8. Preferably, the inside diameter and 20 the length of each tube should be the same for all tubes in the central bunch or the annular bunch. By this means equal flow may be obtained through all of the tubes.
Alignment pins, fins, centering vanes, spacers and other conventional means are used to symmetrically space the tubes and conduits with respect to each other and to hold same in stable alignment without obstructing the free-flow of the feedstreams in the central and annular interstitial zones.
The downstream exit ends of the plurality of 30 annular and central bunches of parallel tubes terminate
200759
In the same plane perpendicular to the longitudinal central axis of the burner. In one embodiment employing pre-mix chambers, to be further described, the ends of the central and/or annular bunch of tubes are retracted upstream from the burner face to provide substantial mixing of the reactants and volatilization of the slurry medium prior to discharge.
The central conduit exit orifice and/or the annular exit orifice may have converging sections. For 10 example, the central conduit exit orifice may comprise a frusto-conical rear portion having a converging angle in the range of about 15° to 90° from the central longitudinal axis of the burner. The rear portion may develop into a normal cylindrical front portion which terminates at the downstream face of the burner. The cylindrical front portion may have a height in the range of•about 0 to 1.5 times its own diameter.
In one embodiment the first conduit downstream outlet comprises a converging frusto-conical rear portion that develops Into a diverging frusto-conical front portion 20 that terminates at the downstream tip of the burner. The converging and diverging angles are in the range of about 15° to 90° with the central longitudinal axis of the burner.
Similarly, said annular exit orifice may comprise a generated converging frusto-conical shaped annular rear portion having a converging angle in the range of about 15° to 90° from the central axis of the frusto-conical section,
said central axis being parallel to the central longitudinal axis of the burner. The rear portion may develop into a generated normal cylindrical annular front portion which 30 terminates at the downstream face of the burner. The
200759
cylindrical front portion may have a height in the range of about 0 to 1.5 times its own width.
In one embodiment, the central conduit exit orifice and/or the annular exit orifice are in the shape of or is generated by an American Society of Mechanical Engineer's standard long-radius nozzle. A further description of said nozzle may be found in "Thermodynamics Fluid Flow and Heat Transmission" by Huber 0. Croft, page 155, First Edition, 1938 McGraw-Hill Book Company.
The burner may be cooled on the outside by means of cooling coils that encircle the outside barrel of the burner along its length. The downstream end of the burner may be provided with a cored face plate through which a coolant is circulated. For example, an annular cooling chamber may encircle the annular exit orifice and/or the central conduit exit orifice. The cooling chamber, central conduit exit orifice and/or the annular exit orifice may constitute a single piece of thermal and wear resistant material such as tungsten carbide or silicon carbide. Any 20 suitable coolant may be employed e.g. water.
In one embodiment of the subject burner, a plurality of high pressure high velocity jet streams of a gaseous material is passed into the central conduit and/or annular passage at various locations along their length.
By this means atomizing of the fuel feedstream and, optionally, mixing it with the oxidant stream may be facilitated. For example, the gaseous material may be passed through a plurality of small diameter passages or holes i.e. about .032 to 0-5Q diameter that lead into said central conduit 30 and/or annular passage.
The gaseous material may be selected from the group consisting"of steam, free-oxygen containing gas, CO N , fuel gas, a recycle portion of the product gas, and mixtures thereof. The gaseous material may be introduced into the burner at a temperature in the range of about ambient to 1500°F. and a velocity in the range of about 100 feet per second to sonic velocity. The pressure of the gaseous material may be in the range of about 76 to 4500 psia and is greater than the pressure of the other feedstreams ]_0 passing through the burner.
The discharge velocity for the material leaving through the central exit orifice is in the range of about 0.5 to 1.5 times, and preferably the same as, the discharge velocity of the material leaving through the annular exit orifice. The streams leaving the two exit orifices mix together and atomization may take place immediately downstream from the face of the burner.
In another embodiment of the invention, additional mixing of the reactant streams is effected in at least one, 20 say 2 to 5 coaxial cylindrical shaped pre-mix chambers in series in.the central conduit and/or at least one, say 2 to 5 annular shaped pre-mix chambers in series in the annular passage. In such case, the downstream ends of the central bunch of helical or parallel tubes are retracted upstream from the face of the burner a distance of 0 to 12, such as about 2 or more, say about 3 to 10 times the minimum diameter of the circular exit orifice and/or the downstream ends of the annular bunch of helical or parallel tubes are retracted upstream from the face of the burner a distance of 0 to 12, 30 such as about 2 or more, say about 3 to 10 times the minimum
2 007 5 9
width of the annular exit orifice. Preferably, the downstream ends of the central and annular bunches of helical or parallel tubes are retracted upstream from the entrance to the first pre-mix chamber in the line. For example, the set back of the ends of the tubes from the entrance to the first pre-mix chamber may be in the range of about 0.1-2.0 times the diameter of the first pre-mix chamber.
In one embodiment, each of the pre-mix chambers in the central conduit except the first are cylindrical shaped and comprises a coaxial cylindrical body portion followed by a coaxial at least partially converging outlet portion. The first cylindrical-shaped pre-mix chamber in the central conduit comprises a normal coaxial cylindrical body portion that discharges directly into the next in line coaxial cylindrical shaped pre-mix chamber. Each pre-mix chamber in the annular conduit except the first is annular shaped and comprises a coaxial generated normal cylindrical annular body portion followed by a coaxial generated converging frusto-conical shaped annular outlet portion. The first annular shaped pre-mix chamber comprises a coaxial generated normal cylindrical annular body portion that discharges directly into the next in line coaxial annular shaped pre-mix chamber. The converging outlet portions of said pre-mix chambers may be made from tungsten carbide or silicon carbide for increased wear resistance.
The size relationship between successive pre-mix chambers in the subject burners may be expressed in the following manner: For burners in which the pre-mix chambers in the central conduit are successively numbered 1 to 5 and/or the pre-mix chambers in the annular passage are
numbered 6-10, then the ratio of the diameter of any one of said central chambers to the diameter of the next central chamber in the line i.e. D :D ; D :D ; D :D ; or D :D may
12 23 3 4 45
be in the range of about 0.2-1.2. The ratio of the length of any one central pre-mix chamber in said central conduit to the length of the next central pre-mix chamber in the line i.e. L :L ; L :L ; L :L ; or L :L may be in the range
12 23 34 45
of about 0.1-1.0. The ratio of the annular width of any one of said annular pre-mix chambers to the width of the next
annular chamber in the line i.e. Wg:Wyj Wy:Wg; Wg:W^; or
W :W may be in the range of about 0.1-1.2. The ratio of 9 10
the length of any one annular pre-mix chamber in said annular passage to the length of the next annular pre-mix chamber in the line, i.e. L *.L ; L :L_; Ln:L ; or L :L may be in the
6 7 7 8 8 9 9 10
range of about 0.1-1.0.
In most other respects the design of this pre-mix embodiment of the burner, including the tubes, passages, orifices, water-cooled face-plate and cooling coils, high pressure high velocity jets of a gaseous material entering 20 said central and/or annular pre-mix chambers, and flow control means are substantially the same as previously described. Further, the temperature, pressure and velocity ranges for the streams of materials passing through the various passages of the burner are substantially the same as those discussed previously.
In the operation of the embodiment of the burner employing pre-mix chambers flow control means may be used to control the flow of the four feedstreams to the tubes and passages in the burner in the same manner as described 30 previously. The feedstreams entering the burner and
-n -
simultaneously and concurrently passing through at different velocities impinge and mix with each other in the first pre-mix chambers. The impingement of one reactant stream, such as the liquid slurry of solid carbonaceous fuel in a liquid medium optionally in admixture with a temperature moderator, with another reactant stream, such as a gaseous stream of free-oxygen containing gas optionally in admixture with a temperature moderator at a higher velocity, causes the liquid slurry to break up into a fine spray. The 10 multiphase mixture produced then successively passes through any remaining pre-mix chambers where additional mixing takes place. As the mixture passes freely through the subject unobstructed burner its velocity changes many times. For example, at various points in the burner the velocity of the mixture may range from about 20 to 600 ft. per sec. As the mixture flows from one pre-mix chamber to the next, the velocity changes are mainly the result of changes in the diameter of the flow path and the quantity and temperature of the mixture. This promotes a thorough mixing of the 20 components. By operating in the region of turbulent flow, mixing may be maximized. Further, direct heat exchange between the materials takes place within the burner. From 0-100 vol. %s say about 5-25 vol. % of the liquids in the feedstreams may be vaporized before the feedstreams leave the burner. By means of converging exit orifices, the feedstreams may be accelerated directly into the reaction zone of the partial oxidation gasifier.
Burning of the combustible materials while passing through the pre-mix zone of the burner may be prevented by 30 discharging the multiphase mixtures at the central and
200759
annular exit orifices at the tip of the burner with a discharge velocity which is greater than the flame propagation velocity. Flame speeds are a function of such factors as composition of the mixture, temperature and pressure. They may be calculated by conventional methods or determined experimentally. The ratio of the discharge velocity for the multiphase mixture being discharged through the central exit orifice to the multiphase mixture being discharged through the annular exit orifice may be in the range of about 0.5 to 10 1-5, such as 1.0.
Depending on such factors as the temperature, velocity, dwell time and composition of the feedstreams; the desired amount of vaporization of liquid carrier; the temperature and amount of recycle gases in the generator; and the desired life of the burner; cooling coils may or may not encircle the outside barrel of the burner along its length. For similar reasons, the burner may or may not be provided with an annular shaped cooling chamber at the downstream end.
The multiphase mixtures simultaneously departing from the central orifice and/or the annular orifice at the downstream tip of the burner mix together downstream from the face of the burner.
Advantageously, by means of the subject burner, the exothermic partial oxidation reactions take place a sufficient distance downstream from the burner face so as to protect the burner from thermal damage.
Liquid hydrocarbon fuels and/or pumpable slurries of solid carbonaceous fuels having a dry solids content in 30 the range of about 30 to 75 wt. %s say about 40 to 70 wt. %
may be passed through the Inlet passages of the subject burner. For example, the fuel streams may be passed through the central and/or annular bunch of tubes. The inlet temperature of the liquid hydrocarbon fuel or the slurry is in the range of about ambient to 500°F., but preferably below the vaporization temperature of the liquid hydrocarbon at the given inlet pressure in the range of about 1 to 300 atmospheres, such as 5 to 250 atmospheres, say about 10 to 100 atmospheres.
The term solid carbonaceous fuels, as used herein to describe suitable solid carbonaceous feedstocks, is Intended to. include various materials and mixtures thereof from the group consisting of coal, coke from coal, char from coal, coal liquefaction residues, petroleum coke, particulate carbon soot, and solids derived from oil shale, tar sands, and pitch. All types of coal may be used including anthracite, bituminous,,sub-bituminous, and lignite. The particulate carbon may be that which is obtained as a by-product of the subject partial oxidation process, or that
which is obtained by burning fossil fuels. The term solid carbonaceous fuel also includes by definition bits of garbage, dewatered sanitary sewage sludge, and semi-solid organic materials such as asphalt, rubber and rubber-like materials including rubber automobile tires which may be ground or pulverized to the proper particle size. Any suitable grinding system may be used to convert the solid carbonaceous fuels or mixtures thereof to the proper size.
The solid carbonaceous fuels are preferably ground to a particle size so that 100? of the material passes
through an ASTM E 11-70 Sieve Designation Standard 1.4 mm oo-
(Alternative No. 14) and at least 80/S passes through an ASTM E 11-70 Sieve Designation Standard 425><<m (Alternative No. 40).
The moisture content of the solid carbonaceous fuel particles is in the range of about 0 to 40 wt. %s such as 2 to 20 wt. %.
The term liquid carrier, as used herein as the suspending medium to produce pumpable slurries of solid carbonaceous fuels is intended to include various materials 10 from the group consisting of water, liquid hydrocarbonaceous material, and mixtures thereof. However, water is the preferred carrier for the particles of solid carbonaceous fuel. In one embodiment, the liquid carrier is liquid carbon dioxide. In such case, the liquid slurry may comprise 40-70 wt. % of solid carbonaceous fuel and the remainder is liquid CO2» The C02~solid fuel slurry may be introduced into the burner at a temperature In the range of about -67°F to 100°F depending on the pressure.
The term liquid hydrocarbonaceous material as used 20 herein to describe suitable liquid carriers and fuels is intended to Include various liquid hydrocarbon materials, such as those selected from the group consisting of liquefied petroleum gas, petroleum distillates and residues, gasoline, naphtha, kerosine, crude petroleum, asphalt, gas oil, residual oil, tar sand oil and shale oil, coal derived oil, aromatic hydrocarbons Csuch as benzene, toluene,
xylene fractions)., coal tar, cycle gas oil from fluid-catalytic-cracking operation, furfural extract of coker gas oil and mixtures thereof.
-U-
2007 59
The term liquid hydrocarbonaceous material as used herein to describe suitable liquid fuels is also intended to include various oxygen containing liquid hydrocarbonaceous organic materials, such as those selected from the group consisting of carbohydrates, cellulosic materials, aldehydes, organic acids, alcohols, ketones, oxygenated fuel oil, waste liquids and by-products from chemical processes for producing oxygenated hydrocarbonaceous organic materials, and mixtures thereof. 10 ' For example in one embodiment, the feedstream comprises a slurry of liquid hydrocarbonaceous material and solid carbonaceous fuel. H^O In liquid phase may be mixed with the liquid hydrocarbonaceous carrier, for example as an emulsion. A portion of the H^O i.e., about 0 to 25 weight % of the total amount of H^O present may be Introduced as steam in admixture with the free-oxygen containing gas. The weight ratio of H20/fuel may be in the range of about 0 to 5, say about 0.1 to 3-
The term gaseous hydrocarbonaceous material as 20 used herein to describe suitable gaseous hydrocarbonaceous fuels is intended to include a gaseous feedstock from the group consisting of ethane, propane, butane, pentane,
methane, natural gas, coke-oven gas, refinery gas,
acetylene tail gas, ethylene off-gas, and mixtures thereof.
Simultaneously with the fuel stream(s), one or more free-oxygen containing gas streamCs). is supplied by way of a free passage ("si in the burner. The free-oxygen containing gas may be passed through the central and/or annular sections at a temperature in the range of about ambient to 15Q0°F.,
-62--
200759
and preferably in the range Of about ambient to 300°F., for oxygen-enriched air, and about 500° to 1200°F., for air, and a pressure in the range of above about 1 to 300 atmospheres, such as about 5 to 250 atmospheres, say about 10 to 100 atmospheres. The atoms of free-oxygen plus atoms of organically combined oxygen in the solid carbonaceous fuel per atom of carbon" in the solid carbonaceous fuel (0/C atomic ratio) may be in the range of 0.5 to 1.95. With free-oxygen containing gas in the reaction zone the broad 10 range of said 0/C atomic ratio may be about 0-5 to 1.7» such as about 0.7 to 1.4. More specifically, with air feed to the reaction zone, said 0/C atomic ratio may be about 0.7 to 1.6, such as about 0.9 to 1.4.
The term free-oxygen containing gas, as used herein is intended to Include air, oxygen-enriched air, i.e., greater than 21 mole % oxygen, and substantially pure oxygen, i.e., greater than 95 mole % oxygen, (the"remainder comprising and rare gases).
The free-oxygen containing gas may be supplied 20 with or without mixture with a temperature moderating gas. The term temperature moderating gas as employed herein is intended to include by definition a member of the group consisting of steam, CO^, , a recycle portion of the cooled and cleaned effluent gas stream from the gas generator, and mixtures thereof.
P. L.B.&A. T
The subject burners as shown in Figures 9—4 may be per.
c2P"7 £ /<P"Y °Perate<^ with the feedstreams passing through alternative passages in the burner. Typical modes of operation before P. L. B. & A.
)4_ or after replacement of fuels are summarized in Tables D?
p.r !H'~ *
£f-l i and M. below.
— : mm *0 jou, i
F.L.B-*7 H - 200759
Table X lists the. materials being Introduced Into p.r_/7"-
. ~ the gasifier by way of the burner and their corresponding ! (? I
symbol. The solid carbonaceous fuel (B), water (C), and liquid hydrocarbonaceous material (E) may be mixed together in various combinations upstream from the burner inlet to produce a pumpable slurry which may be introduced into the burner and then passed through one of the several free-flow P- L. B. & A. 3Z"
passages of the burner as shown in Table "35. For example,
per. (T)~
& j £ /At ^he first entry in Table £■£ shows that a pumpable slurry
stream comprising solid carbonaceous fuel (B) in admixture P. L. B & a with water (C) may be passed through the central ana/or c£#~l annular bunch of tubes In the burner i.e. Fig. \ or
Whenever a fuel stream is introduced into the burner by way of the central and/or bundles of tubes, a corresponding stream of free-oxygen containing gas is simultaneously passed through the related central conduit and/or annular passage. Some additional examples follow:
(1) separate streams of free-oxygen containing gas may be passed through said central and/or annular bunches
of tubes; and simultaneously separate corresponding streams of a pumpable slurry of solid carbonaceous fuel in a liquid carrier or a hydrocarbonaceous fuel may be passed through the related central conduit and/or annular passage.
(2) separate streams of free-oxygen containing gas may be passed through said central conduit and said annular passage; while simultaneously a corresponding stream of liquid hydrocarbonaceous material is passed through the related central and/or annular bunches of tubes; and simultaneously a pumpable slurry of solid carbonaceous fuel
P. L. B. & A.
per
#-/c 18*1
P.L. B.& A.
par
/ C '
40
p. L. B. & A-
VP-
p«r -
&sti c in a liquid carrier may be passed through the bunch of said tubes, if. any.
(3) separate streams of free-oxygen containing gas may be passed through said central and/or annular bunches of tubes; while simultaneously a corresponding stream of liquid hydrocarbonaceous material is passed through the related central conduit and/or annular passage; and simultaneously a pumpable slurry of solid carbonaceous fuel in a liquid carrier may be passed through the unoccupied passage, if any.
TABLE 23
Material
Free-oxygen Containing Gas Solid Carbonaceous Fuel Water Steam
Liquid Hydrocarbonaceous Material Temperature Moderating Gas Gaseous Hydrocarbon Fuel
TABLE MTV
Symbol
A B C D E F G
Central
Central
Annular
Annular
Conduit
Bunch of Tubes
Passaee
Bunch of Tubes
A
B+C
A
B+C
A+D
B+C
A+D
B+C
B+C
A
B+C
A
A
B+C
B+C
/ A
B+C
A
A
B+C
A
B+C+E
A
B+C+E
B+C+E
A+D
B+C+E
A+D
A
E
A
E
A+D
B+E
A+D
B+E
B+E
A+D
B+E
A+D
A+D
E
A
B+C
E
A
E
A
B+C
A
E
A
E
A
B+C
A
A
G
A -
B+C
A
G
A+D
E
A
E+F
A
E+F
E+F
A+D
E+F
A+D
Other modes of operation of the subject invention t?
are possible in addition to those shown in Table 55.
/ : V
2007!
For examplej jet streams of a gaseous material may be simultaneously introduced into the central conduit and/or annular passage, as previously described.
When one of the fuel streams is a liquid hydrocarbon or the liquid carrier for the slurry of solid carbonaceous fuel is a liquid hydrocarbonaceous material premature combustion within the burner may be avoided by -one or more of the following:
(.1) keeping the fuel below its autoignition temperature, 10 (.2) including water in the solid fuel slurry,
(3) using air or air enriched with oxygen i.e. up to about 40 vol. % 02>
(4) mixing steam with the air,
(5) employing about 0 retraction of the ends of the central and annular bunches of tubes from the face of the burner. In such case, the free-oxygen containing gas such as substantially pure oxygen may be separately discharged from the burner without first contacting the fuel stream.
(6) discharging the multiphase mixture at the central and annular exit orifices at the tip of the burner with discharge velocities that exceed the flame propagation velocity.
The subject burner assembly is inserted downward through a top inlet port of a compact unpacked free-flow noncatalytic refractory lined synthesis gas generator, for example as shown in coassigned U. S. Patent No. 3,544,291. The burner extends along the central longitudinal axis of the gas generator with the downstream end discharging 30 directly into the reaction zone.
The relative proportions of the reactant feedstreams and optionally temperature moderator that are introduced into the gas generator are carefully regulated to convert a substantial portion of the carbon in the fuel e.g., uc to about 90# or more by weight, to carbon oxides; and to maintain an autogenous reaction zone temperature in the
-&c-
<r» £
200759
range of about 1700° to 3500°F., preferably in the range of 2000° to 2800°F.
The dwell time in the reaction zone is in tfcf range of about 1 to 10 seconds, and preferably in the range of about 2 to 8. With substantially pure oxygen feed to the gas generator, the composition of the effluent gas from the gas generator in mole % dry basis may be as follows:
P. L. B. & A.
, H0 10 to 60, CO 20 to 60, C0o 5 to 40, CHj, 0.01 to 5,
er //Y fir
H2S+C0S nil to 5, N2 nil to 5, and nil to 1.5. With air
feed to the gas generator, the composition of the generator
P. L. B. & A
fh=
per <& I (o /ffm effluent gas in mole % dry basis may be about as follows:
H0 2 to 30, CO 5 to 35, CO, 5 to 25, CH, nil to 2, 2 2 flr *
H2S+C0S nil to 3, N2 45 to 80, and 0.5 to 1.5. Unconverted carbon and ash are contained in the effluent gas stream.
The hot gaseous effluent stream from the reaction zone of the synthesis gas generator Is quickly cooled below the reaction temperature to a temperature In the range of about 250° to 700°F. by direct quenching in water, or by indirect heat exchange for example with water to produce 20 steam in a gas cooler.
Advantageously, In another embodiment of the subject invention the subject two-section burner may be used as the preheat burner during start-up of the gasifier, as well as the production burner. Start-up procedures are thereby simplified. Previously, time was lost when the gas preheat burner was replaced by the production burner, and the gasifier cooled down. Now the gasifier may be brought up to operating temperature and held there by simultaneously passing a gaseous or liquid hydrocarbonaceous fuel i.e. fuel 30 gas, with or without mixture with H20, through the central icrt
~ 2 j'jl d84
200759
. ana/or annular bundle(s) of tubes and a free-oxygen containing gas, preferably air, with or without mixture with
H 0 through the associated central conduit and/or annular 2
passage. Alternately, the gaseous or liquid hydrocarbonaceous fuel i.e. fuel gas with or without mixture with H^O may be passed through the central conduit and/or annular passage in the burner and the air with or without mixture with H 0
2
may be passed through the associated central and/or annular bundleCs) of tubes. The fuel gas and air are mixed together to produce a well-distributed blend. Burning of the mixture by substantially complete combustion then takes place in the reaction zone of the gas generator at a temperature in the range of about 2000 to 4500°F., such as about 2000 to 3000°F.
and at an absolute pressure In the range of about 0.56 to
,300 atmospheres, and preferably at 1 atmosphere. The products of the complete combustion are removed from the reaction zone.
For example, they may be vented to the atmosphere.
By this means, the reaction zone is heated to the temperature required for ignition of the autothermal partial oxidation reaction of the principal fuel selected from the group consisting of a pumpable slurry of solid carbonaceous fuel, liquid or gaseous hydrocarbon fuel, and mixtures thereof with a free-oxygen containing gas and with or without a temperature moderator. For example, the auto-
ignition temperature may be in the range of about 2000 to
2700°F. At this point, the fuel gas, with or without mixture H 0, is phased out of the tubes or conduits in 2
which it is flowing In the central and/or annular section (.s) of said two-section burner with a uniformly decreasing rate of flow that varies from maximum rate to 0 over a period in the range of about 1-3600 seconds, say about
200759
60-1800 seconds. Simultaneously, the principal solid carbonaceous fuel slurry or liquid hydrocarbonaceous fuel,
with or without mixture with H^O, is phased into the remaining portion of said fuel gas and replaces the phased-out portion of the fuel gas with a uniformly increasing rate of flow that varies from 0 to maximum over the same period of time.
Simultaneously with the replacement of the fuel, or alternatively when the fuel gas has been completely 10 replaced in the burner by the principal fuel, the free-oxygen containing gas i.e. air, with or without mixture with is phased out with a uniformly decreasing'rate of flow that varies from maximum to 0 over a period in the range of 1-3600 seconds, say about 60-1800 seconds. Simultaneously, another free-oxygen containing gas i.e. oxygen-rich gas or substantially pure oxygen for the production of syngas Is phased into the same line to replace the air at a uniformly fincreasing rate of flow that varies from 0 to maximum over the same period of time. Further, the rates of flow of the 20 free-oxygen containing gas with or without mixture with HO and if necessary the weight ratio ^O/fuel in the reaction zone are adjusted so as to continuously maintain the temperature and the weight ratio H^O/fuel in the reaction zone at design conditions for the partial oxidation of said principal fuel.
Partial oxidation of the principal fuel takes place downstream In the reaction zone of the free-flow noncatalytic gas generator at design conditions which include an autogenous temperature in the range of about 1700° to 3500°F. 30 a pressure in the range of about 1 to 300 atmospheres, an
-w -
2
'j b fr3
3
atomic ratio of oxygen to carbon in the range of about 0.5 to 1.7, say to 0.8 to 1,2, and an H20/fuel weight ratio in the range of about 0 to 5.0, such as 0.1 to 3.
The hot gaseous effluent stream from the reaction zone 5 of the synthesis gas generator is quickly cooled below the reaction temperature to a temperature in the range of about 250° to 700°F. by direct quenching in water, or by indirect heat exchange for example with water to produce steam in a gas cooler. The gas stream may be cleaned and 10 purified by conventional methods.
A more complete understanding of the invention may be had by reference to Figures 4 and 5 of the drawings which show the subject invention in detail. Although the drawing illustrates preferred embodiments of the invention, it is 15 not intended to limit the subject invention to the particular apparatus or materials described. Like parts in the embodiments of Figures 1 to 5 are given like reference numerals.
Referring to Figs. 4 and 5, Fig. 4 is a schematic 20 representation of one embodiment of the invention showing control means for the continuous operation of a synthesis gas generator while phasing out one fuel and simultaneously phasing in another without depressurizing. Further, the control means may be used for rapidly changing throughput 25 levels - up or down over the flow range for which the two-
section burner shown in designed. By this means adjustments may be made to control the amount of raw effluent gas produced, and to provide for a change in demand for the product gas. Further, another use for the control system 30 is to maintain the desired composition of the product gas when possible to do so by adjustments to the flow rates of one or more of the reactant streams. Thus, by the subject
-90
200759
" * flow control system, the flow rates for all of the reactant streams are separately ana independently controlled so that the temperature and weight ratio of H^O to fuel in the reaction zone are maintained at design conditions and within desired operating ranges for the fuel being reacted. If necessary the atomic ratio of free-oxygen to carbon in the fuel in the reaction zone may also be controlled within design conditions.
While the control system shown in Figure 4 is 10 specifically designed for the combination of feedstocks comprising a solid carbonaceous fuel slurry and a liquid hydrocarbonaceous fuel, by simple modifications to the means for changing the flow rate of the streams up or down in a manner similar to that as described below, the system may be used to control other combinations of solid carbonaceous fuel slurries, and liquid, or gaseous hydrocarbon fuels.
Two-section burner 1 is mounted in central flanged inlet 30 located In the upper head of conventional refractory lined free-flow synthesis gas generator 41 along 20 the central longitudinal axis. The reactant streams enter through the upstream end of burner 1, pass downward therethrough, and are discharged through the downstream end. Burner 1 is designed so that the required system output for steady-state operation may be achieved or even exceeded by a specified amount when the flow rate through all passages in both sections of the two-section burner is a maximum. The control system can Independently change up or down the flow rate of any one or more of the reactant streams in lines 187, 190, 167, 170, 50, 60, 70 and 73. By this 30 means the temperature in the reaction zone 31 is maintained at the desired operating temperature. Further, the weight
ratio H20 to fuel, and if necessary the atomic ratio of free oxygen to carbon in the fuel in the reaction zone may be maintained at design conditions whether one or both sections of the burner are employed to step-up or step-down production of product gas.
Two-section burner 1 comprises a central section and a concentric annular section. The central section substantially comprises: central cylindrical conduit 2 having a closed upstream end and an open downstream end, 10 central bunch of parallel tubes 3 supported longitudinally in central passage 4 of central conduit 2 and having open upstream ends that pass through and are sealed in the closed upstream end of central conduit 2 and are in communication with central cylindrical shaped manifold 19, Inlet feed pipe 20 connected to and in communication with central manifold 19, and inlet feed pipe 25 connected to and in communication with the closed upstream end of central conduit 2. The annular section comprises: outer cylindrical concentric conduit 5 which is closed at the 20 upstream end and open at the downstream end, annular passage 6 between the outside diameter of central conduit 2 and the inside diameter of outer conduit 5 along its length, annular bunch of parallel tubes 7 supported longitudinally in said annular passage 6 and having open upstream ends that pass through and are sealed in the closed upstream annular end of outer conduit 5 and are in communication with annular manifold 28, inlet feed pipe 29 connected to and in communication with annular manifold 28, and inlet feed pipe 35 connected to and In communication with the upstream 30 closed end of outer conduit 5.
-73-^
I
L. B. & A.
►
2QQ759 :
9 *•
' . i*
While the downstream tips of, central bunch of tubes 3 and annular bunch of' tubes 7 are shown in Fig- 4 as being flush with the face of burner 1, in other embodiments of the two-section burner the downstream tips of the central and/or annular bunch(.es) of tubes may be retracted upstream to provide at least one premix zone as shown in Fig. 5
Although central bunch of tubes 3 and annular bunch of tubes 7 are shown in Fig. 4 as being parallel to each other and to the burner axis, in another embodiment of
the two-compartment burner which is shown and described per No. »<vS?/,V^
c 'ih '
in coassigned U. S. Patent Application-S^N. 21^054 i.e. Fig. 5 thereof,
the central and/or annular bunches of tubes may be helical-shaped. By this means the swirling reactant streams passing down through the central and/or annular bundles of helical tubes; and separately down through the helical passages on the outside of the helical bundles of tubes may impinge together either'in the premix zones or downstream in the reaction zone and may be thereby intimately 2.0 mixed together. Combustion efficiency of the burner is thereby improved.
In Fig. 4 for purposes of illustration, the principal fuel may be for example a solid carbonaceous fuel slurry i.e. coal-water slurry in line 42. The stand-by fuel is a liquid hydrocarbonaceous fuel i.e. residual oil in line 160. Of course, the principal fuel may have been chosen to be any liquid or gaseous hydrocarbonaceous fuel or a coal-oil slurry. The metered feedstream of solid carbonaceous fuel slurry in line 42 is split into two fuel feedstreams 43 and 30 44 by separate flow control means in each line. Similarly,
r.y
72 - 2.^
the metered feedstream of liquid hydrocarbonaceous fuel in line 160 is split into two fuel feedstreams 161 and 162 by separate flow control means in each line. In the subject process, the remaining portions of the principal fuel stream(s) being phased out of line 50 and/or line 60 are respectively mixed in lines 15 and/or 16 with the stand-by fuel stream(s) being phased into line 167 and/or line 170*
In a similar manner, the metered feedstream of free-oxygen containing gas in line 62 i's split into two 10 feedstreams 63 and 64 by separate flow control means in each line.
1^0 may be in admixture with the fuels, in lines 160 and 42 or the free-oxygen containing gas in line 62. Alternatively, as shown in Fig. 1, at least a portion i.e. 10-100 vol. % of the H^O may be provided as steam. Thus,
steam in line 180 is split Into two feedstreams 181 and 182 by separate flow control means in each line. By this means as shown in Fig. 4, steam in linejs) 187 and/or 190 preferably may be mixed respectively in line(s) 18 and/or 17 with the 20 free-oxygen containing gas flowing into one or both sections of the burner. In a similar manner (not shown) steam from line(s) 187 and/or 190 may be respectively supplied to the fuel in line(s) 15 and/or 16. By this scheme, controlled amounts of steam may be Introduced into and mixed with the stream(s) of free-oxygen containing gas and/or fuel upstream from the burner.
The weight or volumetric rate of flow for that portion of the feed flowing through each of the feedlines to the burner Is a function of the burner design. For 30 example, the burner passages may be sized so that one-third
-?h~
of the total quantity of the solid carbonaceous fuel slurry flowing through line 42 plus the liquid hydrocarbonaceous fuel flowing through line 160 may be discharged through central bunch of tubes 3 at a specified velocity range. Simultaneously, the remaining two-thirds of the total quantity of solid carbonaceous fuel slurry plus liquid hydrocarbonaceous fuel may be discharged through annular bunch of tubes 7 at a specified velocity range.
Valves 183, 184, 163, 164, 77, 76, 65 and 66 10 may be manually or automatically operated to obtain a wide open position to a completely closed position. The rates that each valve may be opened and closed is also controllable. In one embodiment to be further described, by closing specific valves one may turndown or sectionalize the burner. The burner may be thereby operated either in the central section i.e. central tubes 3 and annular passage 4, or in the outer annular section I.e. annular tubes 7 and annular passage 6, or with both the central and annular sections of the burner in simultaneous operation. 20 Operation of the system while employing only the central section of the burner will be described first. The portion of the slurry feedstream In line 43 is pumped into the reaction zone 31 of synthesis gas generator 4l by way of positive displacement pump 45 equipped with speed control 46, line 47, flow measurer and transmitter 48, line 49, valve 77, lines 50 and 15, inlet 20 of burner 1, central manifold 19, and central bunch of tubes 3*
The slurry flow rate through line 43 is controlled by the speed of positive displacement pump 45- In order 30 to phase out the slurry flowing through line 43, this speed
<^N ^ '/>
j, . r,
, * is continuously decreased from maximum to zero over a period in the range of about 1 to 3600 seconds, such as about 60 to 1800 seconds, say about 300 to 1000 seconds. Flow recorder-controller with transmitter 51 comprises a microcomputer means which is programmed with the desired time vs. decreasing flow rate curve. The rate of slurry flow in line 47 is measured and a signal a is provided by flow transmitter 48 corresponding to the flow rate of the slurry in line 43. Flow recorder-controller 51 receives signal a, 10 compares it with a signal representing the desired flow rate for that moment, and provides a corresponding adjustment signal to speed control 46 to adjust the speed of pump 45 downward so that the charge slurry flowing in line 49 assumes a given decreased flow rate for that moment in the phase-out period. The new slurry rate is measured and the cycle is repeated. By this means, repeated adjustments to the rate of flow are made and the slurry flowing in line 50 is phased out.
Simultaneously with the phasing out of the portion 20 of principal slurry fuel flowing in line 43, the portion of stand-by liquid hydrocarbonaceous fuel flowing in line 161 is phased In over the same period of time. Flow recorder-controller with transmitter 171 comprises a microcomputer means which Is programmed with the desired time vs. increasing flow rate curve. The rate of oil flow in line 161 is measured and a signal m Is provided by flow transmitter 165 corresponding to the flow rate of the oil in line 161.
Flow recorder-controller 171 receives signal m, compares it with a signal representing the desired flow rate for that 30 moment and provides a corresponding adjustment signal to valve 163 to open wider so that the charge oil in line 166
.. * assumes a given increased flow rate for that moment in the phase-in period. The new oil rate is measured and the cycle is repeated. By this means, repeated adjustments to the rates of flow of the principal and stand-by fuels may be made so that the oil flowing in line 167 may be phased into line 15 in an amount that compensates for the reduced amount of solid carbonaceous fuel slurry flowing in line 50.
During or after the period that the portion of principal solid carbonaceous slurry fuel from line 43 is 10 phased out and the portion of stand-by liquid hydrocarbon fuel from line 161 is phased in, the weight ratio of temperature moderator to fuel in the reaction zone may be controlled for example at design conditions, or substantially constant i.e. less than - 10% variation, by increasing or decreasing the flow rate of the temperature moderator. Accordingly in the subject example, simultaneously with the phase-out of the coal-water slurry a supplemental amount of H20 from an external source may be phased in over the same period of time. Thus, in Fig. 4, a portion of the steam in line 180 20 is passed through line .181 and is phased into line 18 where it mixes with the free-oxygen containing gas from line 70. Flow recorder-controller with transmitter 191 comprises a microcomputer which is programmed with the desired time vs. increasing flow rate curve.
The rate of steam flow in line 181 is measured and a signal s is provided by flow transmitter 185 corresponding to the flow rate of the steam in line 181.
Flow recorder-controller 191 receives signal s, compares it with a signal representing the desired flow rate for that 30 moment and provides a corresponding adjustment signal to valve 183 to open wider so that the charge steam in line 186 assumes
-11
a given increased flow rate for that moment in the phase-in period. The new steam rate is measured and the cycle is repeated. By this means, repeated adjustments to the rate of steam flow are made and the steam.flowing in line 187 is phased into line 18 in an amount that will maintain the weight ratio of H20 to fuel in the reaction zone at design conditions.
In another embodiment the weight ratio I^O/fuel in the reaction zone is adjusted up or down by controlling the steam rate as described previously in order to obtain a desired temperature in the reaction zone and composition of the product gas.
Simultaneously with or after the phasing out of the principal fuel, the phasing in of the stand-by fuel, and optionally with or without the phasing in or out of the steam depending on the nature of the fuels, the free-oxygen containing gas may be adjusted up or down so as to control the temperature in the reaction zone for example at design
' a j,
p.U- * conditions, or substantially constant I.e. less than -
%*r-"^'Z 2Q 200°F. variation. Thus, in the present example in Fig. It, a portion of the free-oxygen containing gas in line 62 is passed through line 63 and is phased into line 18 where It mixes with the steam, If any, from line 187 as previously described. Flow controller 74 is programmed with the desired time vs.* flow rate curve. The period of adjustment Is the same as that for the fuel and steam streams. The adjustment to the oxygen flow rate may be up or down depending on the nature.of the fuel streams and the addition of steam, if any. In the subject example, the oxygen flow rate will be 3%}° 4 increased to satisfy the_ additional requirements for the
"partial oxidation of a liquid hydrocarbon in comparison with "a solid carbonaceous fuel.
2
>
t •
I ...
The rate of free-oxygen containing gas in line 63 is measured and a signal b is provided by flow transmitter 67 corresponding to the flow rate of the free-oxygen containing gas in line 63- Flow recorder-controller with transmitter 74 comprises a microcomputer means which receives signal b, compares it with a signal representing the desired flow rate for that moment, and provides a corresponding adjustment signal to valve 65 to open wider so that the charge free-oxygen containing gas in line 68 assumes a given 10 increased flow rate for that moment in the phase-in period.
The new free-oxygen containing gas rate is measured and the cycle is repeated. By this means repeated adjustments to the rate of oxygen flow are made and the free-oxygen containing gas flowing in line 70 is phased into line 18 in an amount that will maintain the temperature in the reaction zone substantially constant.
In another embodiment, the free-oxygen containing gas rate is adjusted up or down to obtain a desired temperature in the reaction zone and composition of the 20 product gas. Alternatively, by the previously described means, the atomic ratio of oxygen to carbon in the reaction zone may be controlled at design conditions i.e. in the range of about 0.5 to 1.7.
Operation of the system while employing only the annular section of the burner is similar to that described previously in connection with the central section of the burner. The portion of the slurry feedstream in line 44 Is pumped Into the reaction zone 31 of synthesis gas generator 41 by way of positive displacement pump 55 30 equipped with speed control 56, line 57, flow measurer and
*! 0 0 7 59.
transmitter 58, line 59, valve 76, lines 6Q and 16, Inlet-29 of burner 1, annular manifold 28, and annular bunch of tubes 7-
The slurry flow rate through line 44 is controlled by the speed of positive displacement pump 55- In order to phase out the slurry flowing through line 44, this speed is continuously decreased from maximum to zero over a period in the range of about 1 to 3600 seconds, such as about 60 to 1800 seconds, say about 300 to 1000 seconds. Flow 10 recorder-controller with transmitter 61 comprises a microcomputer which is programmed with the desired time vs. decreasing flow rate curve. The rate of slurry flow in line 57 is measured and a signal d is provided by flow transmitter 58 corresponding to the flow rate of the slurry in line 44. Flow recorder-controller 61 receives signal d, compares it with a signal representing the desired speed at that moment, and provides a corresponding adjustment.signal to speed control 56 to adjust the speed of pump 55 downward so that the charge slurry flowing in line 59 assumes a given 20 decreased flow rate for that moment in the phase-out period. The new slurry rate is measured and the cycle is repeated. By this means, repeated adjustments to the rate of flow are made and the slurry flowing in line 60 is phased out.
Simultaneously with the phasing out of the portion of principal slurry fuel flowing in line 44, the portion of stand-by liquid hydrocarbonaceous fuel flowing in line 162 is phased in over the same period of time. Flow recorder-controller with transmitter 172 comprises a microcomputer means which is programmed with the desired time vs. increasing 30 flow rate curve. The rate of oil flow in line 162 is
-7 tjv
"f v x vj! / ^ v;
# • ■ s ^ ^,-r/ ^
measured and a signal q is provided by flow transmitter 168 corresponding to the flow rate of the oil in line 162. Flow recorder-controller 172 receives signal q, compares it with a signal representing the desired flow rate at that moment, and provides a corresponding adjustment signal to valve 164 to open wider so that the charge oil In line 169 assumes a given increased flow rate for that moment in the phase-in period. The new oil rate is measured and the cycle is repeated. By this means, repeated adjustments to the rates 10 of flow of the principal and stand-by fuels may be made so that the oil flowing in line 170 may be phased Into line 16 in an amount that compensates for the reduced amount of solid carbonaceous fuel slurry flowing in line 60.
During or after the period that the portion of principal solid carbonaceous slurry fuel from line 44 is phased out and the portion of stand-by liquid hydrocarbon fuel from line 162 is phased in the weight ratio of temperature moderator to fuel in the reaction zone may be controlled for example at design conditions, or substantially 20 constant I.e. less than - 10% variation by increasing or decreasing the flow rate of the temperature moderator. Accordingly, in the subject example, simultaneously with the phase-out of the coal-water slurry a supplemental amount of H20 from an external source may be phased in over the same period of time. Thus, In Fig. 4, a portion of the steam in line 180 is passed through line 182 and is phased into line 17 where It mixes with the free-oxygen containing gas from line 73- Flow recorder-controller with transmitter 192 comprises a microcomputer means which is programmed with the 30 desired time vs. increasing flow rate curve.
. 200759
The rate of steam flow In line 182 is measured and a signal t is provided by flow transmitter 188 corresponding to the flow rate of the steam in line 182. Flow recorder-controller 192 receives signal t, compares it with a signal representing the desired flow rate at that moment, and provides a corresponding adjustment signal'to valve 184 to open wider so that the charge steam in line 189 assumes a given increased flow rate for that moment in the phase-in period. The new steam rate is measured and the cycle is 10 repeated. By this means, repeated adjustments to the rate of steam flow are made and the steam flowing in line 190 Is phased into line 17 in an amount that will maintain the weight ratio of E^O to fuel in the reaction zone at design conditions.
In another embodiment the weight ratio I^O/fuel in the reaction zone Is adjusted up or down by controlling the steam rate as described in the manner described previously in order to obtain a desired temperature in the reaction zone and composition of the product gas.
Simultaneously with or after the phasing out of the principal fuel, the phasing in of the stand-by fuel, and optionally with or without the phasing in or out of the steam depending on the nature of the fuels, the free-oxygen containing gas may be adjusted up or down so as to control the temperature In the reaction zone for example at design conditions, or substantially constant i.e. less than - 200°F.
^ ;..•*******"" (r varia-tion* Thus in the present example, In Fig. a portion of the free-oxygen containing gas in line 62 is passed through line 64 and is phased into line 17 where it mixes • —'With the steam, if any, from line 190 as previously described.
VCM
-> i'm
::l~
Flow recorder-controller with transmitter 75 comprises a microcomputer means which is programmed with the desired time vs. flow rate curve. The period of adjustment is the same as that for the fuel and steam streams. The adjustment to the oxygen flow rate may be up or down depending on the nature of the fuel streams and the addition of steam, if any. In the subject example, the oxygen flow rate 'will be increased to satisfy the additional requirements for the partial oxidation of a liquid hydro-10 carbon in comparison with a solid carbonaceous fuel.
The rate of free-oxygen containing gas In line 64 is measured and a signal e is provided by flow transmitter 71 corresponding to the flow rate of the free-oxygen containing gas in line 64. Flow recorder-controller 75 receives signal e, compares it with a signal representing the desired flow-rate for that moment, and provides a corresponding adjustment signal to valve 66 to open wider so that the charge free-oxygen containing gas in line 72 assumes a given increased flow rate for that moment in the phase-in 20 period. The new free-oxygen containing gas rate is measured and the cycle is repeated. By this means repeated adjustments to the rate of oxygen flow are made and the free-oxygen containing gas flowing In line 73 Is phased into line 17 in an amount that will maintain the temperature in the reaction zone substantially constant.
In another embodiment, the free-oxygen containing gas rate Is adjusted up or down to obtain a desired temperature in the reaction zone and composition of the product gas. Alternatively, by the previously described 30 means, the atomic ratio of oxygen to carbon in the reaction zone may be controlled at design conditions i.e. in the
% -
range of about 0.5 to 1.7*
The previously mentioned time vs. flow rate curves for programming flow controllers 191, 192, 171, 172, 51, 6l, 74 and 75 may be determined by conventional calculations based on heat and weight balances for the entire system.
In another embodiment, the parameters for said calculations and any others may be measured by conventional detectors and the signals responsive thereto may be fed to an overall control means or computer 40. The input to flow 10 control means 40 may be manual or a signal from a computer,
analyzer, or sensor. Control means 40 comprises conventional circuits and components for providing signals i.e. pneumatic or electronic to operate said speed controls and valves.
In control means 40, the computer calculated values or the manually inserted set points for the desired rates of flow at specific moments for the various streams are compared respectively with.the signals a, d; s, t; m, q; and b, e. For example, responsive to signal(s) a and/or d, control means 40 may automatically control pump speed control(s) 20 46 and/or 56 by sending signal(s) c and/or f respectively to flow-recorder-controller(s) 51 and/or 61. Alternatively, signal(s) c and/or f may be fed directly to speed control(s) 46 and/or 56 respectively. Signals i and/or g from control means 40 may be employed to close respectively solid carbonaceous fuel slurry valves 77 and/or 76. In another embodiment, for example flow recorder-controller 51 may receive signal a from flow transmitter 48 and signal c from control means 40 and compute the speed adjustment signal for the operation of speed control 46.
In a similar manner, responsive to signal(s) s and/or t, control means 40 may automatically control steam
-sm -
/7 .i ;/ ;
■ j :tv • ■ (J c/^
. valve(s) 183 and/or 184 by sending signal(s) u and/or r respectively to flow-recorder-controller(s) 191 and/or 192.
Similarly j responsive to signalCs). m and/or q,
control means 40 may automatically control liquid hydrocarbonaceous fuel valveCs) 163 and/or 164 by sending signalCs) w and/or x respectively to flow-recorder-controller(.s) 171 and/or 172.
Also, similarly, responsive to signal(s) b and/or e, control means 40 may automatically control 10 free-oxygen containing gas valve(s) 65 and/or 66 by sending signalCs) j and/or h respectively to flow-recorder-controller ( s ) 7^ and/or 75-
FIG. 5 is a vertical longitudinal schematic representation of another embodiment of the subject two-section burner. Two pre-mix chambers in series are located in the central conduit in the central section and also in the annular passage in the annular section. The ends of the central bundle of tubes in the central section and the annular bundle of tubes in the annular section are retracted upstream from 20 the face of the burner. In FIG. 5, burner 80 comprises central conduit 8l which in part constitutes the wall 82 between central passage 83 and coaxial radially spaced annular passage 84, two rows of a central bundle of parallel tubes 85 that pass longitudinally through the upper portion of central passage 83 and having upstream ends 86 that pass through tube sheet 87 making a gastight hermetic seal therewith, and downstream ends 88 which are retracted upstream from face 89 at the downstream end of burner 80, coaxial concentric radially spaced outer conduit 2.0 surrounding said 30 annular passage 84 along its length, two rows of an annular bundle of parallel tubes 95 that pass longitudinally through
annular passage 84 with upstream ends" 96 pass'^^^-'
tube sheet 97 and making a g'astight seal therewith and having downstream ends 98 retracted upstream from face 89,
annular manifold 100 in communication with the upstream ends
96 of said annular bundle of tubes 95, manifold 101 which may be cylindrical-shaped in communication with the upper ends
86 of said central bundle of tubes 85, inlet means 102 for -
introducing a first feedstream into said central manifold
101, Inlet means 103 for introducing a second feedstream into said centra], passage 83 and in the interstices surrounding said central bundle of tubes 85, inlet means 104 for introducing a third feedstream into said annular manifold 100,
inlet means 105 for introducing a fourth feedstream into said annular passage 84 and Into the interstices surrounding the annular bundle of tubes 95, cooling coils 106 which
<?o encircle the outside diameter of outer conduit "&Q. along its length, and cored cooling chamber 107 at the downstream tip of the burner.
• ~
Disc shaped central tube sheet 87 closes off central passage 83 below its upstream end. Similarly,
annular shaped tube sheet 97 closes off annular passage 84 below its upper end. Conventional means i.e. welding,
turning, crimping, threading, rolling may be employed to provide a pressure and gastight hermetic seal or joint where the central and annular bunches of tubes penetrate the respective tube sheets. Mechanical pressure fittings and coupling devices may be also employed.
Plate 108 which may be disc-shaped seals off the upper end of central conduit 81. The space between plate 108 and"tube sheet 87. constitutes said central manifold 101. By this means, for example, a portion of a first reactant
- •"? »
;?54 8(o
. * feedstream in feed pipe 102 may be introduced intone
"5 ri p.
£ .UM
\
manifold 101 and then split into a plurality of streams which pass through tube sheet 87 and the individual tubes in central bundle 85. Annular shaped disc 109 seals off the upper end of annular passage 84. The space between annular disc 109 and annular tube sheet 97 constitutes annular manifold 100. Simultaneously and concurrently with the Introduction of the first reactant feedstream, the third reactant feedstream in feed pipe 104 may be 10 Introduced into annular manifold 100, split into a plurality of streams which pass through tube sheet 97 and the individual tubes in annular bundle 95-
individual tubes in annular tube bundle 95 in a fixed parallel nontouching relationship with respect to each other, the inside of outer conduit 90, and the outside diameter of central conduit 8l. Similarly, wall brackets or tube spacers 116 hold the individual tubes in central tube bundle 85 in a fixed parallel nontouching relationship with 20 respect to each other and the inside diameter of central conduit 81.
FIG. 5 are shown as comprising two separate coaxial central pre-mix chambers 117 and 118 in series in central conduit 83, and two separate coaxial annular pre-mix chambers 119 and 120 In series in annular passage 84, the pre-mix zone of other embodiments of the subject Invention may actually comprise one or more, such as 2 to 5 coaxial central and/or annular pre-mix chambers. Each central pre-mix chamber, 30 except for the first chamber in the line, comprises a coaxial cylindrical body portion 121 followed by a coaxial at least
Wall brackets or tube spacers 115 hold the
While the pre-mix zones in the embodiment in
7 it
. 2 ^ 0
. " partially converging frusto-conical outlet portion 122 that ^ may optionally develop into a normal cylindrical portion 123. This outlet portion is shown in FIG. 5 as a converging central nozzle 124 which terminates at the downstream face of the burner. Optionally, nozzles 124 and 133 to be further described may be made from a thermal and wear resistant material i.e. silicon carbide or tungsten carbide.
The first central pre-mix chamber in the line may have a straight coaxial cylindrical body portion 125j that 10 discharges through circular orifice 126 directly into the next in line central coaxial pre-mix chamber 118. Preferably, the inlet to the first central pre-mix chamber 117 is a portion of a converging frusto-conical shaped section 127-
Each of the coaxial annular shaped pre-mix chambers 120 except the first annular shaped chamber 119 comprises a coaxial generated normal cylindrical annular body portion 130 followed by a coaxial generated at least partially converging frusto-conical shaped annular outlet portion 131 that may optionally develop into a coaxial generated normal 20 cylindrical annular portion 132. This outlet portion is shown in FIG. 5 as a converging annular exit nozzle 133 which terminates at the downstream face of the burner. The first coaxial annular shaped pre-mix chamber 119 comprises a coaxial generated normal cylindrical annular body portion 134 that discharges through annular orifice 135 into the next in line coaxial annular shaped pre-mix chamber 120. Preferably, the inlet to the first annular shaped pre-mix chamber 119 comprises a portion of a coaxial generated converging frusto-conical shaped section 136. 30 Cored faceplate 107 comprises a front portion 137
at the extreme tip of the burner, which may be flat or curved, and which contains a coaxial central annular shaped
-2^
«j • i i i i i k ii
200759
cooling chamber 138 surrounding the central conduit exit nozzle 124 and/or a coaxial radially spaced annular shaped cooling chamber 139 surrounding said annular exit nozzle 133
^.L.B.&A. a1- .j-kg burner. The cooling chamber may be joined
S
P*r L to the otherwise flat burner tip such as shown in FIG. 4, or c#/
it may be an extension of the central and outer conduits.
Cold cooling water in line 140 enters annular shaped cooling chamber 139, splits by means of baffles and flows about
180°, and leaves by way of an opposite outlet which is
connected to outer coils 106. Cooling water is introduced
Into central annular cooling chamber 138 by way of line 145
which is connected to passage 146 that passes longitudinally down through wall 82 in central conduit 8l. The cool water splits by means of baffles, flows about 180° around central cooling channel 138, and leaves by way of an opposite coaxial longitudinal passage (not shown) similar to passage 146 but in another location in wall 82.
Optionally, a gaseous feedstream selected from the group consisting of steam, free-oxygen containing gas, CO2,
N2, fuel gas, recycle portion of the product gas, and mixtures thereof may be introduced into at least one of the central and/or annular pre-mix chambers by way of at least one Inlet pipe 149 which is connected to at least one longitudinal passage 147 in wall 82 of central conduit 81,
"57' and at least one branch passage 148 connecting longitudinal passage 147 with said pre-mix chambers.
While the central bundle of tubes 85 and the annular bundle of tubes 95 are shown in Figure 5 as comprising a plurality of parallel tubes, In another embodiment of the burner depicted In Figure 5 of coassigned $K| b I U-s. Patent No.
patent ?pp"l 1 cat 1 nn Serial No.—212,1'054 filed in Hie U. G-r
200759
P. L. B. S A.
p^j. (£7= PaLenL and Trademark Off-ice on -Docombor 3; 1000 and Figure otyj (0 / I 13 of our published French Patent Application No. 8027516, and which are incorporated herein by reference, the central and annular bundles of tubes may be helical shaped.
Although modifications and variations of the invention" may be made without departing from the spirit and scope thereof, only such limitations should be imposed as are indicated in the appended claims.
•' :?34
<{o
Claims (12)
1. "A process for producing gaseous mixtures comprising H2* CO, CC^f entrained particulate carbon, and at least one material from the group consisting of 1^0, N2, H2S' ^OS, per /£EL- ch4 ' K- and ash in a free-flow non-catalytic partial I 6 oxidation gas generator, including employing a one or two- section burner having at least one first fluid conduit or * p, & A- group of conduits to provide a first fluid passage or ddjc*ceat passages, and at least one rolafccd radially spaced second (j j/M fluid conduit surrounding said first fluid conduit or group of conduits to provide at least one annular second fluid passage therebetween and having either a central or a central and annular exit orifice at the tip of the burner, and changing from one reactant feedstream to another without shutting down or depressurizing the system, the process „ i . B. & comprising the combination of the steps of: r • i-f-l5' (1) passing a first reactant stream of first solid perhenzxnb«fcve defined) jY\ & ) carbonaceous fuel slurry or hydrocarbonaceous fuel^with or ~ i p. & A- without mixture with a temperature moderator through either • "• u' fluid P&sscvgca or le^st oneejr soJ<3 fit*? d r JfJ at least one of said first^ese—second fluid paaoagoc-^ Jsg' jb Pi' simultaneously passing a separate reactant stream of free-oxygen containing gas with or without mixture with a p L. B. & A- temperature moderating gas through the unused passage or ct4iacen(- fw ...» passages in said burner which are related to a passage per g%) I'SM through which said first reactant stream in (1) is flowing^ (3) mixing together said reactant streams from (1) and (2) to produce a well-distributed blend, and reacting said mixture by partial oxidation in the reaction zone of said gas generator at an autogenous temperature in the . in*A range -of nboufc 1700° to 3500°F., a pressure in the range irf qPj (o l^l f L about 1 to 300 atmospheres, an atomic ratio of oxygen/carbon in the range of about 0.5 to 1.7, and a weight ratio / (>" H20//^ue''" in rani3e of obou-t 0 to 5.0; ^ (4) phasing out of the fluid passage or passages in L. B. & A. ''"••'iJ^which it is flowing in said burner said stream of first cArt i ^ solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with a temperature moderator, said _phasing out being with a uniformly decreasing rate of flow . \J W / v.-V t; . that varies from maximum to 0 over a period of time in the ' fty> range of ab#wt 1-3600 seconds; and simultaneously phasing ^ 0 0 7 5 9 said stream of second solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with temperature moderator into the same fluid passage in said burner at a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time, and mixing the phased-in stream with the remaining portion of said stream of first solid carbonaceous fuel slurry or hydrocarbonaceous fuel with or without mixture with a temperature moderator flowing therein; and (5) adjusting the flow rate of the reactant stream of free-oxygen containing gas with or without mixture with a temperature moderator passing through the burner and if necessary introducing supplemental H20 into the reaction zone, so as to adjust the free oxygen/carbon atomic ratio and the weight ratio I^O/fuel in the reaction zone to design conditions for the partial oxidation reaction.
2. A process according to Claim 1 in which in step ^ (5) the temperature in the reaction zone is maintained substantially constant and the weight ratio J^O/fuel is maintained in the range of aboufc. 0.1 to 3.0.
. 3. A process according to Claim 1 or Claim 2 in which •firsV" reaoranl stream said hydrocarbonaocouG- f ue-1- is a pumpable slurry of a solid carbonaceous fuel in a liquid carrier from the group consisting of water, liquid hydrocarbon fuel, and mixture thereof. # v
4. A process according to Claim 3 wherein said solid carbonaceous fuel is selected from the group consisting of coal, lignite, coke from coal, char from coal, coal liquifaction residues, particulate carbon, petroleum coke, solids derived from oil shale, tar sands and pitch, concentrated sewer sludge, bits of garbage, rubber, and , mixtures thereof.
5. A process according to any of Claims 1 to 4 wherein -said burner comprises one-section with the first fluid conduit ^ a per ttbL (pfj c I jf-vj 200^59 P. L. B. & A. retracted upstream from the face of the burner a distance per HlP" about 3 to 10 times the minimum diameter of the central ££I Q exit orifice at the tip of the burner to provide a pre-mix zone.
6. A process according to Claim 5 wherein said pre-mix zone comprises 2 to 5 coaxial cylindrical shaped pre-mix chambers in series.,
7. A process according to any of Claims 1 to 4 wherein said burner comprises two-sections with the first fluid group P L B & A conduits in the first section comprising a bunch of parallel tubes whose downstream tips are retracted upstream from the face of the burner a distance of aboufe 0 to 12 times the minimum diameter of the central exit orifice at the tip of the burner, and the first fluid group of conduits in the second section comprises an annular bunch of parallel tubes whose downstream tips are retracted upstream from the face of the burner a distance of about 0 to 12 times the minimum width of the annular exit nozzle at the tip of the burner.
8. A system for controlling the introduction of a plurality of reactant streams into the reaction zone of a partial oxidation gas generator comprising: a burner comprising at least one first fluid conduit or group of conduits to provide a first fluid passage or passages and a second fluid conduit surrounding each of said first fluid conduit or group of conduits to define a second fluid passage therebetween; two separate burner inlet lines connected to each of said first fluid conduit or conduits and to each of said second fluid conduit, respectively; conduit means including four feed lines for connecting four different material feedstreams to said two burner inlet lines for introducing said feedstreams into the burner, one respective pair of said feed lines being associated with each burner inlet lines, said burner discharging said . . feedstreams or mixtures thereof into said reaction zone; a - 2 ifn separate flow rate sensing means and a separate flow rate ^Li984 controller in each of said feed lines for independently —'-3VE0' ' sensing the flow rate for each material flowing through a 13 p, L. B. & A p.rJtE... Hj 4 /m 200759 P. L. B. & A. particular feed line and providing a signal corresponding to the actual flow rate for that feedstream; and a control means for receiving said signals from said flow rate sending means and for comparing each actual flow rate signal with a manual or automatically computed and inserted input signal representing the desired flow rate or set point at that moment for each feedstream and providing a corresponding adjustment signal for separately operating the flow rate controller in that particular feed Mine, and for independently controlling the flow rate for each feedstream entering the burner at that moment such that one feedstream in each pair of feedstreams is phased out with a uniformly decreasing rate of flow that varies from maximum to 0 over a period of time UT.... per... /. .j-hQ range o£ about 1-3600 seconds; and simultaneously £ /Pxyj ' ' a different feedstream is phased into the same feed line with a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time.
9. A control system according to Claim 8 wherein the P. L. B.&A. „ first feedstream comprises steam, the second feedstream ,\ Cos kvef<)/">bfcfr>T d<fiAmJ P®r comprises a liquid ov gaocous hydrocarbonaceous fuel, the I o 7 f 1 third feedstream comprises a pumpable solid carbonaceous fuel slurry, and the fourth feedstream comprises a free- oxygen containing gas, and each flow rate controller for independently controlling the rate of flow of the first, second, and fourth feedstreams is a flow control valve, and the flow rate controller for independently controlling the rate of flow of the third feedstream is a speed controlled pump.
10. A process for producing gaseous mixtures comprising #2r CO, CO2, entrained particulate carbon, and at least one P.L. B.&A. material from the group consisting of H00, H0, H~S, COS, per CH4' an<^ ask ;'-n free-flow non-catalytic partial I oxidation gas generator, wherein, for starting up and operating the gas generator by employing a two-section burner having a central section and an annular section with two "*.. ,,r separate fluid passage means in each section, and changing ™ from one reactant feedstream to another without shutting " -i-JUL J934 down or depressurizing the system, the process comprises the 075? steps of: a nWh (1) passing a first reactant stream of solid carbonaceous i de^neeo rnjrf fuel slurry or hydrocarbonaceous fuel^with or without mixture w H2O through either the first or second fluid passage means in # the central section of said burner, and/or simultaneously . . - C«i .^VP passing a second reactant stream of hydrocarbonaceous fuel with 2~S\ ] or without mixture with 1^0 through either the third or fourth fluid passage means in the annualar section of said burner; (2) simultaneously passing a separate reactant stream of air with or without mixture with ^0 through the unoccupied fluid passage means in each of the central and/or annular sections of said burner which are associated with said fluid passage means through which said stream of first hydrocarbonaceous fuel with or without mixture with 1^0 are passing; (3) mixing together said reactant streams from (1) and (2) to produce a well-distributed blend, and burning said mixtures by substantially complete combustion in the reaction zone of said gas generator at a temperature in the range 2000° to 3500°F. and i a pressure in the range to 300 atmospheres; (4) phasing out of the fluid passage means in which it is flowing said first reactant stream, said phasing out being with a uniformly decreasing rate of flow that varies from maximum to 0 over a period of time in range 1-3600 seconds; simultaneously phasing in a stream of principal solid carbonaceous fuel slurry or hydrocarbonaceous fuel^with or without mixture with 1^0 into % :\M" the same fluid passage means at a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time and mixing with the remaining portion of and replacing the phased out portion of said first stream; simultaneously phasing out of the ' _ 95 _ 6 2 7 JUL 1984 2J0759 fluid passage means in which it is flowing said separate reactant stream of air said phasing out being with a uniformly decreasing rate of flow that varies from maximum to 0 over a period of time in the range 1-3600 second; and simultaneously phasing in a replacement stream of free-oxygen containing gas with or without mixture with 1^0 into the same fluid passage means at a uniformly increasing rate of flow that varies from 0 to maximum rate over the same period of time and mixing with the remaining portion of and replacing the phased out portion of said separate reactant stream of air; and (5) adjusting the flow rate of the reactant stream of free-oxygen containing gas with or without mixture with 1^0 passing through the burner, and if necessary introducing supplemental 1^0 into the reaction zone so as to adjust the free oxygen/carbon atomic ratio and the weight ratio l^O/fuel in the reaction zone at design conditions for partial oxidation.
11. A process for producing gaseous mixtures comprising H2 and CO, the process being substantially as hereinbefore described with reference to any one of the accompanying drawings.
12. "A system for controlling the introduction of a plurality of reactant streams into the reaction zone of a partial oxidation gas generator, the system being substantially as hereinbefore described with reference to any one of the accompanying drawings. -TEXACO DEVELOPMENT CORPORATION by their authorised agents: P.L.BERRY & ASSOCIATES per: /-j-
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/272,419 US4400180A (en) | 1980-12-03 | 1981-06-10 | Partial oxidation process |
US06/272,420 US4394137A (en) | 1980-12-03 | 1981-06-10 | Partial oxidation process |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ200759A true NZ200759A (en) | 1984-11-09 |
Family
ID=26955506
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ200759A NZ200759A (en) | 1981-06-10 | 1982-05-26 | Producing hydrogen-and carbon monoxide-containing gas mixtures by partial oxidation of carbonaceous fuels |
Country Status (8)
Country | Link |
---|---|
AU (1) | AU549751B2 (en) |
CA (1) | CA1172044A (en) |
DE (1) | DE3220546A1 (en) |
FR (1) | FR2507615B1 (en) |
GB (1) | GB2099843B (en) |
IT (1) | IT1151794B (en) |
NL (1) | NL8202327A (en) |
NZ (1) | NZ200759A (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2141815B (en) * | 1983-06-16 | 1986-07-30 | Boc Group Plc | Method and apparatus for burning fuel |
GB2141532B (en) * | 1983-06-16 | 1986-07-02 | Boc Group Plc | Method of combustion and burners |
GB2164951A (en) * | 1984-09-26 | 1986-04-03 | Shell Int Research | Method and apparatus for producing synthesis gas |
IN167217B (en) * | 1985-04-16 | 1990-09-22 | Dow Chemical Co | |
US5324336A (en) * | 1991-09-19 | 1994-06-28 | Texaco Inc. | Partial oxidation of low rank coal |
DE19928581C2 (en) * | 1999-06-22 | 2001-06-28 | Thermoselect Ag Vaduz | Process and device for the disposal and utilization of waste goods |
CN1295305C (en) * | 2004-12-10 | 2007-01-17 | 华东理工大学 | Pressure gasification reactor and its industrial application |
DE102005018981A1 (en) | 2005-04-23 | 2006-10-26 | Basf Ag | Preparing acetylene by partial thermal oxidation in a reactor exhibiting a burner with execution holes, comprises mixing an use material for bringing it to the reaction directly before the flame reaction zone in the holes of the burner |
FR2900937B1 (en) * | 2006-05-15 | 2008-08-22 | Peugeot Citroen Automobiles Sa | METHOD FOR INHIBITING THE DEPOSITION ON A METAL SURFACE OF PRODUCTS SUCH AS GUMES, AND A METAL PIECE THUS OBTAINED |
JP5166910B2 (en) | 2008-01-29 | 2013-03-21 | 三菱重工業株式会社 | Coal gasifier startup method and starter |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1152783B (en) * | 1961-08-28 | 1963-08-14 | Metallgesellschaft Ag | Burner for the thermal conversion of gaseous and / or vaporous or liquid hydrocarbons and / or other fuel gases with oxygen-containing gases and processes for operating the burner |
US3528930A (en) * | 1968-05-29 | 1970-09-15 | Texaco Inc | Production of synthesis gas |
US3847564A (en) * | 1970-01-23 | 1974-11-12 | Texaco Development Corp | Apparatus and process for burning liquid hydrocarbons in a synthesis gas generator |
US3758037A (en) * | 1971-10-04 | 1973-09-11 | Texaco Development Corp | Fuel burner and process for gas manufacture |
US3929429A (en) * | 1974-09-26 | 1975-12-30 | Texaco Inc | Fuel gas from solid carbonaceous fuels |
DE2703921C3 (en) * | 1977-01-31 | 1980-09-11 | Basf Ag, 6700 Ludwigshafen | Process for commissioning or making a reactor operational for the partial oxidation of non-volatile liquid or solid fuels |
US4144997A (en) * | 1977-10-12 | 1979-03-20 | Phillips Petroleum Company | Control of multiple fuel streams to a burner |
-
1982
- 1982-04-27 GB GB8212202A patent/GB2099843B/en not_active Expired
- 1982-05-26 NZ NZ200759A patent/NZ200759A/en unknown
- 1982-05-26 CA CA000403754A patent/CA1172044A/en not_active Expired
- 1982-06-01 DE DE19823220546 patent/DE3220546A1/en active Granted
- 1982-06-09 AU AU84696/82A patent/AU549751B2/en not_active Ceased
- 1982-06-09 IT IT21788/82A patent/IT1151794B/en active
- 1982-06-09 FR FR8210051A patent/FR2507615B1/en not_active Expired
- 1982-06-09 NL NL8202327A patent/NL8202327A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
GB2099843B (en) | 1985-01-30 |
FR2507615A1 (en) | 1982-12-17 |
AU8469682A (en) | 1982-12-16 |
FR2507615B1 (en) | 1985-11-08 |
GB2099843A (en) | 1982-12-15 |
CA1172044A (en) | 1984-08-07 |
IT1151794B (en) | 1986-12-24 |
NL8202327A (en) | 1983-01-03 |
DE3220546C2 (en) | 1991-10-10 |
DE3220546A1 (en) | 1983-01-27 |
AU549751B2 (en) | 1986-02-13 |
IT8221788A0 (en) | 1982-06-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4490156A (en) | Partial oxidation system | |
US4394137A (en) | Partial oxidation process | |
US4353712A (en) | Start-up method for partial oxidation process | |
EP0127273B1 (en) | Burner and partial oxidation process for slurries of solid fuel | |
US4525175A (en) | High turn down burner for partial oxidation of slurries of solid fuel | |
US4400180A (en) | Partial oxidation process | |
US4400179A (en) | Partial oxidation high turndown apparatus | |
US4491456A (en) | Partial oxidation process | |
US4443228A (en) | Partial oxidation burner | |
US4392869A (en) | High turndown partial oxidation process | |
US4351647A (en) | Partial oxidation process | |
US4351645A (en) | Partial oxidation burner apparatus | |
US4386941A (en) | Process for the partial oxidation of slurries of solid carbonaceous fuel | |
US20170137284A1 (en) | Various methods and apparatuses for multi-stage synthesis gas generation | |
US9663363B2 (en) | Various methods and apparatuses for multi-stage synthesis gas generation | |
US4888031A (en) | Process for partial oxidation of a liquid or solid and/or a gaseous hydrocarbon-containing fuel | |
US3945942A (en) | Fuel burner and process for gas manufacture | |
US4338099A (en) | Process for the partial oxidation of slurries of solid carbonaceous fuels | |
WO2013158343A1 (en) | Various methods and apparatuses for multi-stage synthesis gas generation | |
US5087271A (en) | Partial oxidation process | |
US4479810A (en) | Partial oxidation system | |
US4371379A (en) | Partial oxidation process using a swirl burner | |
US4364744A (en) | Burner for the partial oxidation of slurries of solid carbonaceous fuels | |
US4371378A (en) | Swirl burner for partial oxidation process | |
EP0759886B1 (en) | A process for the manufacture of synthesis gas by partial oxidation of a liquid hydrocarbon-containing fuel using a multi-orifice (co-annular) burner |