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US2695264A - Visbreaking of heavy hydrocarbonaceous materials - Google Patents

Visbreaking of heavy hydrocarbonaceous materials Download PDF

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Publication number
US2695264A
US2695264A US203112A US20311250A US2695264A US 2695264 A US2695264 A US 2695264A US 203112 A US203112 A US 203112A US 20311250 A US20311250 A US 20311250A US 2695264 A US2695264 A US 2695264A
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tar
zone
temperature
flashing
collecting
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US203112A
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Wilfred O Taff
Weikart John
Richard W Eustis
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Standard Oil Development Co
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Standard Oil Development Co
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Priority to US203112A priority Critical patent/US2695264A/en
Priority to GB22815/51A priority patent/GB700137A/en
Priority to FR1048640D priority patent/FR1048640A/en
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils

Definitions

  • the present invention relates hydrocarbons.
  • the presentinvention provides: anaoperation'of; this type.
  • An increase inf'the gasolinefyieldfof 2.-'l-0%ffonifeedinay represent, depending on the type of feed, a 20-100% increase ⁇ in ⁇ gasoline yield.
  • Visbreaking fori this purpose include temperatures of about 780- 950 F., pressures of about 200-1500 p. s. i. g. and visbreaker feed rates of 1-75 volumes per hour of oil at 60@ F. per cracking volume above 750 F.
  • the temperature maybe about 20-50 F. higher than that conventionally used-for-the same feed,
  • a virgin crude distillation residuum boiling3above about 800 F. may be supplied from line 1 by feed pump 3 via line 5 to visbreaking coil 7 substantially at the' temperature at which it is recovered from the crude still, sayrat about 500-750 F.
  • Coil 7 is arranged in furnace: 9 in such a manner as to provide a preheating sectionfmaintained at about 700-850 F., a heating sec- Y 3 d tion maintained at about 780-950 F. and a relatively similar temperature distribution.
  • Other modifications short soaking section maintained substantially at the within the spirit of the invention will appear to those temperature of the heating section.
  • the feed is heated skilled in the art.
  • API liquid volume of residuum feed may be supplied through gsfsgrfggffog at 210 F 2g 43(1)?) line 13 at a temperature of about 400-650 F. as will Surinam,percent f f: 3 03 2, 71 appear more clearly hereinafter.
  • the quenched product Conradson Carbon. wt. prcen 15.7 19.7 is flashed by means of pressure release valve 14 into a 20 10 mfgvcmm DStuaton 513 698 lower portion of the baled section of tiash tower 15 at 5%, i F 879 93o a temperature of about 450-800 F. and a pressure of FBP.
  • a throughput tial pressure controllers e.g., a throughput tial pressure controllers.
  • the tar level in tar pot 21 is of 15 v./v./hr. in the visbreaking coil section mantaine so adjusted that a substantially constant tar hold up and above 750 F. and a ash tower pressure of about l0() a tar residence time of about 0.5-5 minutes, preferably p. s. i. g.
  • Other reaction conditions and the results obclosely approaching the lower limit, is provided at the tained using residuum A are tabulated below.
  • a stream of tar is Comparison of runs F and G indicates that run G which circulated from the bottom of tar pot 21 via line 29 by employed the lower tar pot temperature, 603 vs. 794
  • the improvement which comprises carrying out said treatzone at a temperature of about 400-600 F. said ashing temperature and for a residence time of about 0.5-5

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Processing Of Solid Wastes (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

Nov. 23, 1954 w. o. TAFF :TAL VISBREAKING OF HEAVY HYDROCARBONACEOUS MATERIA Fild Dee. 28, 1950 m. 1M E lmv mm Mw Hl l LD 5E T No 9 AW s .am i im W D .E E F p o C Q m M o L W n| bo L @c V .l 5. 9
y 2,695,264 Patented Nov. 23, 1954 VISBREAKING -OF I-IEA/"Y: HYDROCARBONA'- 5 CEQUSTMATERIALS:
Wilfred 0. Talr and John^Weiliart, Cranford, and Richard W; Eustis, Fanwood, N. J., assignorsto StandardOil Development Company, a corporation of Delaware Application-December 28,4- 1950,-Serial N o. Y203,112 I s Claims. (ci.Vv 1961-50) to 'a method of Vtreating 15 More specifically, the in vention pertains The present invention relates hydrocarbons.
In relningcrude'oihthe'first stepfisnormally a simple distillation orl topping to produce distillate fractions and "a heavy residue. In-orderto'obtain-rnaximum yields of high quality; motor fuels-, allffractions boiling above distillationboiling"above about 800i F: doesnot,A as such, represent a feed stock suitable forcatalytic-icrackm fatory catalytic cracking feedstocks from'these residues; viscosity reduction or visbreaking. is :one of the mostwidely used.
Visbreaking involves atreatment of reduced crude" or 45 the like at temperatures of about 780-950 F. and pres= suresof vaboutl -200-1500 p; -s.- i. g.V at *feedfrates of--1-75 volumes per hour of oil at 60 F.; per'cracking volume above 750 F. to produce bya mild'type of thermal: crackingrabout 5-'15 vola per -cent of gasoil, about 5 -15 vol. lper cent. of gasoline and about 85-70 volrpercent-'of 50 heavy 'fuel' oil. Specific :conditions 'Within'thef'ranges specified depend onrthe. type of the visbreaker'feed; The
fining. The presentinvention provides: anaoperation'of; this type.
It is, therefore, the principal object of this invention 75 to provide improved means -forvisbreakingvheavyfpetroleum residues lof the type specified, permitting the: production tof maximum yields Tof motorand distillate' fuels andrelatively small..yields. of ahighnualty. heavy, fuel'ioil.
the subsequent description of the invention whereinrefmore-severe than those of Other lobjects and advantages willzfappearvfrom l 80:
2 Y erence will benracle to the.acccunpanyingl drawing;.th`e s xngle .figure of which isl .a (semidiagrammatical illustra? tion of a1system-su-1tabletocarryout a preferred-,embodit hasrnowf been found that the-thermal Azcracking :sevof the*` visbreaking foperationmay; be.- substantially t hezzonejin' \vhichit'is separatedY` from hghtenvlsbreakerv products".v Tar..l temthe effluent of 'the visbreakingzone `from"visbreaking temperatures of .about'78`0'950` F; depending; onzthe type "of'feed'rto'a tempera-tureof about .500g-'800 F: prrorfto f Whenoperatng'in"this manner, the'gasolme -yield-fobtained-finvthe visbrea'king process vitself -rnayibe increasedy by abouti-'10%' on-'feed 'the same' n on feed-of high quality loWfsediment-fuel 1Aoil'. An increase inf'the gasolinefyieldfof 2.-'l-0%ffonifeedinay represent, depending on the type of feed, a 20-100% increase `in` gasoline yield. Visbreaking fori this purpose include temperatures of about 780- 950 F., pressures of about 200-1500 p. s. i. g. and visbreaker feed rates of 1-75 volumes per hour of oil at 60@ F. per cracking volume above 750 F. As in conconventional operation, with- 1n the ranges specified. Particularly, the temperature maybe about 20-50 F. higher than that conventionally used-for-the same feed,
typesuofnoperations,v when incorporated into the rprocess of the invention: The @tube i and tanlc type arrangement providing extensive"soakingsspaceifor the feed-.at Jvis'f` breaking .conditionsnafords definitely less significantim#y provements.
Having :setl'fortli its fobje'cts and general fnatureyf invention will be bestunderstood from'thefmor'edetailed description hereinafter read with refcrenceftofthefdraw ing.A The fsystem illustrated.y thedrawingfhessentially af-'a'shtower V15'fprovicledfwith a'tar pot "21 'and atar pot quench circuit 29, 33, 35. e functions and coaction ofi-these-elements will be presently described in connechydrocarbonaceous residues.
In operation, a virgin crude distillation residuum boiling3above about 800 F. may be supplied from line 1 by feed pump 3 via line 5 to visbreaking coil 7 substantially at the' temperature at which it is recovered from the crude still, sayrat about 500-750 F. Coil 7 is arranged in furnace: 9 in such a manner as to provide a preheating sectionfmaintained at about 700-850 F., a heating sec- Y 3 d tion maintained at about 780-950 F. and a relatively similar temperature distribution. Other modifications short soaking section maintained substantially at the within the spirit of the invention will appear to those temperature of the heating section. The feed is heated skilled in the art. in coil 7 to the temperatures mentioned in the order in The advantages afforded by the present invention will dlcated at a pressure of about 100-1500 p. s. 1. g. C011 5 be further illustrated by the following comparative exdmeusions and oil feed rate are so correlated that the perimental data Two different crude residua were oil residence time at visbreaking temperatures exceeding treated in a pilot plant designed and operated substan- 750 F. will be about 0.8-30 minutes, corresponding to tially as described above with reference to the drawing. an oil throughput of about 75-2 volumes of liquid oil per These feed stocks had the following inspections.
volume of visbreaking coil per hour (v./v./hr.). 10 Table I The visbroken product is withdrawn at visbreaking pressure and a temperature of about '780950 F. in mixed vapor-liquid phase via line 11 wherein it is preferably quenched to a temperature of about 500-800 F. by the addition of product tar from line 13. For this 15 Resduum Residuum A. B
purpose about 0.5-1.5 liquid volumes of product tar per GvitY, API liquid volume of residuum feed may be supplied through gsfsgrfggffog at 210 F 2g 43(1)?) line 13 at a temperature of about 400-650 F. as will Surinam,percent f f: 3 03 2, 71 appear more clearly hereinafter. The quenched product Conradson Carbon. wt. prcen 15.7 19.7 is flashed by means of pressure release valve 14 into a 20 10 mfgvcmm DStuaton 513 698 lower portion of the baled section of tiash tower 15 at 5%, i F 879 93o a temperature of about 450-800 F. and a pressure of FBP. F 948 948 Recovery, wt. percent 13. 0 7. 0
about 1D0-200 p. s. r. g. Stripping steam is admitted to flash tower 15 via lines 17 at a point below the feed point of line 11 to aid in the removal of distillate prod- 25 The tar recovered from the tar pot in each case was ucts including gasoline and gas oil which leave tower 15 blended to a constant Saybolt Furol viscosity of 175 overhead through line 19 to be further worked up in seconds at 122 F. with the same gas oil range iiux stock conventional fractionation and catalytic cracking equipin accordance with accepted conventional practice. ment, not shown. These fuel oil blends were then tested for their sedi- Heavy tar of a boiling range suitable for inclusion in ment characteristics by the same filtration procedure at heavy fuel oil is collected in tar pot 21 and handled the same conditions and the sediment removed was retherein as follows. Product tar is withdrawn via line 23 ported as weight percent. Fuel oil blends indicating and passed to storage at a rate of about (16S-0.95 liquid sediments in excess of .5% are considered unsatisfactory volumes per liquid volume of residuum feed, controlled from sedimentation characteristics. by valve 25 which is operated by conventional level con- 35 The visbreaking experiments were carried out at a trol means 27 such as conventional ball float or diiferenvisbreaking coil pressure of 350 p. s. i. g., a throughput tial pressure controllers. The tar level in tar pot 21 is of 15 v./v./hr. in the visbreaking coil section mantaine so adjusted that a substantially constant tar hold up and above 750 F. and a ash tower pressure of about l0() a tar residence time of about 0.5-5 minutes, preferably p. s. i. g. Other reaction conditions and the results obclosely approaching the lower limit, is provided at the tained using residuum A are tabulated below.
Table Il Quench to Line Flash Tower s d Ot Gasomeerit Run Temp., Rate Flash TM Pot lind .ggf F. Tenga, vxgif- Tzerltrrlie -f-- e neng ma F?" Tage gg' 1 ssn 796 794 19 15. s 1.8
residuum feed rates here specified. A stream of tar is Comparison of runs F and G indicates that run G which circulated from the bottom of tar pot 21 via line 29 by employed the lower tar pot temperature, 603 vs. 794
means of pump 31 through a cooler 33 and via line 3S F., and shorter time, l vs. 19 minutes, produced a fuel back into the tar pot Z1 at a point above the withdrawal oil of satisfactory sedimentation characteristics while run point of the circulating tar stream. The temperature of F with high temperature and long time conditions in the cooler 33 and the tar circulation rate through line 35 are 60 tar pot produced an unsatisfactory product. It has been so adjusted that the tar pot temperature is maintained previously stated that increased cracking severity deat about 400-650 F. This may be accomplished by grades fuel oil quality as to sediment but this does not circulating about 0.25-5 liquid volumes of tar per liquid qualify the results above since cracking severity as measvolume of product tar through line 35 at a temperature ured conventionally by gasoline yield is constant. In of about 2O0Jf50 F. A third tar stream may be with- 65 order to obtain a satisfactory fuel oil without using the drawn from tar pot 21 and passed through line 13 to process of the invention, the cracking severity and conline 11 to serve as the quenching medium in line 11 as version must be reduced and hence gasoline yields will described above. be reduced and heavy fuel oil yield increased.
The system of the drawing permits of various modi- Another example in which a residuum of diiferent lications. For example, the quench could be added at 70 character was used at the operating condition previously the flash zone rather than in the transfer line to provide cited is summarized in Table III below for residuum B.
Table III Quench to Line Flash Tower a/ Sedi- B 'r P t (iwnii/eilt ar o me Ilg Yield Per- Temp cent o F Tsnp., 'l/lime,
Q S 787 786 17 13. 7 (l) R.- 920 530 0. 77 605 530 1 13. 5 0. 42
1 Too high to be determined using this test procedure. Experiments indicate that this value is in the range of 1-2 0.
is, therefore, a preferred embodiment of the present invention.
It has also been found that superior feed stocks for the purposes of the invention compared to tube-and-tank procedures.
The foregoing description What is claimed is:
1. In the process of viscosity breaking heavy hydrocarbonaceous residues by a thermal treatment carried out at temperatures of about 780-950 F., pressures of about 200-1500 p. s. i. g. and treating times corresponding to feed rates of about 1-75 volumes per hour of feed of 60 F. per volume of reactor space above 750 F.
the improvement which comprises carrying out said treatzone at a temperature of about 400-600 F. said ashing temperature and for a residence time of about 0.5-5
and withdrawing distillate fractions from zone.
2. The process of claim 1 in which said material is quenched to a temperature of about 500-800 F. prior to dashing, by the addition of tar withdrawn from said collecting zone.
3. The
he process of claim 1 1'11 Which said collecting zone temperature and residence times are maintained within the lower brackets of the ranges specified.
References Cited in the le of this patent UNITED STATES PATENTS Number Name Date 2,105,122 Kimball et al. Jan. 11, 1938 2,152,147 Nafsinger Mar. 28, 1939 2,187,708 Cibulka et al. Jan. 16, 1940 2,189,016 yMiller et al. Feb. 6, 1940 2,209,154 Downey `Iuly 23, 1940 2,358,150 Cooke Sept. 12, 1944 2,385,325 Bailey Sept. 25, 1945

Claims (1)

1. IN THE PROCESS OF VISCOSITY BREAKING HEAVY HYDROCARBONACEOUS RESIDUES BY A THERMAL TREATMENT CARRIED OUT AT TEMPERATURES OF ABOUT 780-950* F., PRESSURES OF ABOUT 200-1500 P.S.I.G. AND TREATING TIMES CORRESPONDING TO FEED RATES OF ABOUT 1-75 VOLUMES PER HOUR OF FEED OF 60* F. PER VOLUME OF REACTOR SPACE ABOVE 750* F. TO PRODUCE A VISBROKEN MATERIAL AND SEPARATING TAR AND DISTILLATE FRACTIONS INCLUDING GASOLINE FROM SAID MATERIAL, THE IMPROVEMENT WHICH COMPRISES CARRYING OUT SAID TREATMENT AT SEVERE CONDITIONS OF TEMPERATURE, PRESSURE AND TREATING TIMES WITHIN THE RANGES SPECIFIED, CONDUCTIVE TO THE PRODUCTION OF RELATIVELY LARGE AMOUNTS OF GASOLINE AND RELATIVELY SMALL AMOUNTS OF TAR, SAID TREATMENT CONDITIONS BEING SUCH AS TO INITATE DEGRADATION OF THE TAR FRACTION TO PRODUCE AN INTOLERABLE PROPORTION OF SEDIMENT IF THE TEMPERATURE WERE MAINTAINED FOR A SUBSTANTIAL PERIOD OF TIME AFTER LEAVING THE REACTOR, QUENCHING SAID VISBROKEN MATERIAL AFTER LEAVING THE REACTOR AND BEFORE SUBSTANTIAL PRESSURE REDUCTION TO REDUCE ITS TEMPERATURE ABOUT 150* TO 280* F., FLASHING SAID MATERIAL AT SAID REDUCED TEMPERATURE INTO A FLASHING ZONE MAINTAINED AT A PRESSURE BELOW SAID SEVERE VISBREAKING PRESSURE, STRIPPING DISTILLATE FRACTIONS OFF SAID FLASHED MATERIAL WITH STEAM IN SAID FLASHING ZONE, COLLECTING TAR IN A ZONE BELOW SAID FLASHING ZONE, MAINTAINING SAID TAR IN SAID COLLECTING ZONE AT A TEMPERATURE OF ABOUT 400*-600* F, BUT BELOW SAID FLASHING TEMPERATURE AND FOR A RESIDENCE TIME OF ABOUT 0.5-5 MINUTES, MAINTAINING SAID COLLECTING ZONE TEMPERATURE BY CIRCULATING TAR FROM SAID COLLECTING ZONE THROUGH A COOLING ZONE AND BACK TO SAID COLLECTING ZONE WITHDRAWING TAR FROM SAID COLLECTING ZONE AT A RATE ADEQUATE TO LIMIT THE TAR RESIDENCE TIME TO THAT SPECIFIED AND WITHDRAWING DISTILLATE FRACTIONS FROM SAID FLASHING ZONE.
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GB22815/51A GB700137A (en) 1950-12-28 1951-10-01 Improvements in or relating to the reduction in viscosity of heavy hydrocarbon residues
FR1048640D FR1048640A (en) 1950-12-28 1951-10-19 Treatment of heavy hydrocarbons

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3296118A (en) * 1960-06-15 1967-01-03 Universal Oil Prod Co Hydroforming with a platinum catalyst
US3309295A (en) * 1962-01-12 1967-03-14 Exxon Research Engineering Co Distillation of heat sensitive compounds
US3322842A (en) * 1965-05-24 1967-05-30 Universal Oil Prod Co Recycle of hydrodealkylation product for hydrogen enrichment
US4389302A (en) * 1981-05-15 1983-06-21 Kerr-Mcgee Refining Corporation Process for vis-breaking asphaltenes
US4508614A (en) * 1982-11-08 1985-04-02 Mobil Oil Corporation Visbreaker performance for production of heating oil
US4522703A (en) * 1981-07-08 1985-06-11 Mobil Oil Corporation Thermal treatment of heavy hydrocarbon oil
US4533462A (en) * 1983-01-07 1985-08-06 Institut Francais Du Petrole Process for the treatment of highly viscous heavy oils at the oil field to effect desalting and transportability thereof
US4778586A (en) * 1985-08-30 1988-10-18 Resource Technology Associates Viscosity reduction processing at elevated pressure
US20070007175A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007174A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007170A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007169A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007172A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007173A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007171A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20080099371A1 (en) * 2006-10-30 2008-05-01 Mccoy James N Process for upgrading tar
US20110000819A1 (en) * 2009-07-01 2011-01-06 Keusenkothen Paul F Process and System for Preparation of Hydrocarbon Feedstocks for Catalytic Cracking

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2463177A1 (en) * 1979-08-07 1981-02-20 Uop Inc Visbreaking with improved quenching before passing to flash zone - using liq. mixt. having relatively low viscosity

Citations (7)

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Publication number Priority date Publication date Assignee Title
US2105122A (en) * 1933-06-20 1938-01-11 Sinclair Refining Co Art of cracking hydrocarbons
US2152147A (en) * 1937-09-22 1939-03-28 Gasoline Prod Co Inc Conversion of hydrocarbon oils
US2187708A (en) * 1936-01-31 1940-01-16 Standard Oil Dev Co Apparatus for inhibiting tar polymerization
US2189016A (en) * 1936-04-02 1940-02-06 Phillips Petroleum Co Process for treating hydrocarbons
US2209154A (en) * 1937-06-15 1940-07-23 Sinclair Refining Co Manufacture of gasoline and fuel oil
US2358150A (en) * 1941-04-04 1944-09-12 Gulf Oil Corp Cracking hydrocarbon oils
US2385325A (en) * 1944-06-19 1945-09-25 Shell Dev Catalytic cracking of petroleum oils

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2105122A (en) * 1933-06-20 1938-01-11 Sinclair Refining Co Art of cracking hydrocarbons
US2187708A (en) * 1936-01-31 1940-01-16 Standard Oil Dev Co Apparatus for inhibiting tar polymerization
US2189016A (en) * 1936-04-02 1940-02-06 Phillips Petroleum Co Process for treating hydrocarbons
US2209154A (en) * 1937-06-15 1940-07-23 Sinclair Refining Co Manufacture of gasoline and fuel oil
US2152147A (en) * 1937-09-22 1939-03-28 Gasoline Prod Co Inc Conversion of hydrocarbon oils
US2358150A (en) * 1941-04-04 1944-09-12 Gulf Oil Corp Cracking hydrocarbon oils
US2385325A (en) * 1944-06-19 1945-09-25 Shell Dev Catalytic cracking of petroleum oils

Cited By (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3296118A (en) * 1960-06-15 1967-01-03 Universal Oil Prod Co Hydroforming with a platinum catalyst
US3309295A (en) * 1962-01-12 1967-03-14 Exxon Research Engineering Co Distillation of heat sensitive compounds
US3322842A (en) * 1965-05-24 1967-05-30 Universal Oil Prod Co Recycle of hydrodealkylation product for hydrogen enrichment
US4389302A (en) * 1981-05-15 1983-06-21 Kerr-Mcgee Refining Corporation Process for vis-breaking asphaltenes
US4522703A (en) * 1981-07-08 1985-06-11 Mobil Oil Corporation Thermal treatment of heavy hydrocarbon oil
US4508614A (en) * 1982-11-08 1985-04-02 Mobil Oil Corporation Visbreaker performance for production of heating oil
US4533462A (en) * 1983-01-07 1985-08-06 Institut Francais Du Petrole Process for the treatment of highly viscous heavy oils at the oil field to effect desalting and transportability thereof
US4778586A (en) * 1985-08-30 1988-10-18 Resource Technology Associates Viscosity reduction processing at elevated pressure
WO2007008403A3 (en) * 2005-07-08 2008-02-28 Exxonmobil Chem Patents Inc Method for processing hydrocarbon pyrolysis effluent
US20100096296A1 (en) * 2005-07-08 2010-04-22 Robert David Strack Method For Processing Hydrocarbon Pyrolysis Effluent
US20070007170A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007169A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007172A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007173A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007171A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
WO2007008403A2 (en) * 2005-07-08 2007-01-18 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
WO2007008396A2 (en) * 2005-07-08 2007-01-18 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
WO2007008424A1 (en) * 2005-07-08 2007-01-18 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
WO2007008423A1 (en) * 2005-07-08 2007-01-18 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
WO2007008396A3 (en) * 2005-07-08 2007-03-08 Exxonmobil Chem Patents Inc Method for processing hydrocarbon pyrolysis effluent
US20070007175A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US8524070B2 (en) 2005-07-08 2013-09-03 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US7465388B2 (en) 2005-07-08 2008-12-16 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US20090074636A1 (en) * 2005-07-08 2009-03-19 Robert David Strack Method for Processing Hydrocarbon Pyrolysis Effluent
US7674366B2 (en) 2005-07-08 2010-03-09 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US20070007174A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US7718049B2 (en) * 2005-07-08 2010-05-18 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US8092671B2 (en) 2005-07-08 2012-01-10 Exxonmobil Chemical Patents, Inc. Method for processing hydrocarbon pyrolysis effluent
US7749372B2 (en) 2005-07-08 2010-07-06 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US7763162B2 (en) 2005-07-08 2010-07-27 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US7780843B2 (en) 2005-07-08 2010-08-24 ExxonMobil Chemical Company Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US20100230235A1 (en) * 2005-07-08 2010-09-16 Robert David Strack Method For Processing Hydrocarbon Pyrolysis Effluent
US20100276126A1 (en) * 2005-07-08 2010-11-04 Robert David Strack Method for Processing Hydrocarbon Pyrolysis Effluent
US8074707B2 (en) 2005-07-08 2011-12-13 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
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