GB2092561A - Sintered high density spherical ceramic pellets - Google Patents
Sintered high density spherical ceramic pellets Download PDFInfo
- Publication number
- GB2092561A GB2092561A GB8205575A GB8205575A GB2092561A GB 2092561 A GB2092561 A GB 2092561A GB 8205575 A GB8205575 A GB 8205575A GB 8205575 A GB8205575 A GB 8205575A GB 2092561 A GB2092561 A GB 2092561A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pellets
- ceramic
- impeller
- density
- bauxite
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000008188 pellet Substances 0.000 title claims abstract description 65
- 239000000919 ceramic Substances 0.000 title claims abstract description 38
- 229910001570 bauxite Inorganic materials 0.000 claims abstract description 24
- 101100234822 Caenorhabditis elegans ltd-1 gene Proteins 0.000 claims 1
- 239000002245 particle Substances 0.000 abstract description 21
- 239000000843 powder Substances 0.000 abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 12
- 230000003116 impacting effect Effects 0.000 abstract description 10
- 238000000034 method Methods 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000003129 oil well Substances 0.000 abstract description 2
- 208000002565 Open Fractures Diseases 0.000 abstract 1
- 230000035699 permeability Effects 0.000 description 17
- 238000005245 sintering Methods 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 239000007789 gas Substances 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 239000000440 bentonite Substances 0.000 description 6
- 229910000278 bentonite Inorganic materials 0.000 description 6
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 229910010293 ceramic material Inorganic materials 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 3
- 229910010271 silicon carbide Inorganic materials 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000005056 compaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XGNZNBRDPPLKTC-UHFFFAOYSA-N aluminium diboride Chemical compound [Al]1B=B1 XGNZNBRDPPLKTC-UHFFFAOYSA-N 0.000 description 1
- FFBGYFUYJVKRNV-UHFFFAOYSA-N boranylidynephosphane Chemical compound P#B FFBGYFUYJVKRNV-UHFFFAOYSA-N 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
- C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
- C01F7/021—After-treatment of oxides or hydroxides
- C01F7/025—Granulation or agglomeration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/14—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic in rotating dishes or pans
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/80—Compositions for reinforcing fractures, e.g. compositions of proppants used to keep the fractures open
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/25—Methods for stimulating production
- E21B43/26—Methods for stimulating production by forming crevices or fractures
- E21B43/267—Methods for stimulating production by forming crevices or fractures reinforcing fractures by propping
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/30—Particle morphology extending in three dimensions
- C01P2004/32—Spheres
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/10—Solid density
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Mining & Mineral Resources (AREA)
- Fluid Mechanics (AREA)
- Environmental & Geological Engineering (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Geochemistry & Mineralogy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Cosmetics (AREA)
Abstract
Spherical sintered ceramic pellets, for example of bauxite, have a density in excess of 95% of the maximum theoretical density of the ceramic and repeated random samples of such pellets indicate an average sphericity of greater than 0.82 with 95% confidence limits. In a process for manufacturing spherical sintered ceramic pellets a sinterable ceramic powder composition having an average particle size up to 5 microns is added to a rotatable table mixer provided with a rotatable impacting impeller. The table is rotated at 10-60 rpm and the impeller is rotated with a tip speed of 25-50 meters per second. Sufficient water is added to cause spherical ceramic pellets to form and 5 to 15 per cent of additional ceramic powder is added. The impeller is then rotated with a tip speed of 5-20 meters per second for 1 to 6 minutes while the table is rotated at 10-60 rpm. The pellets are dried at 100-300 DEG C and subsequently furnaced to maximum density. If bauxite is the selected sinterable ceramic powder it will preferably have a maximum average particle size of 4 microns. The pellets may be used for propping open fractures in a gas or oil well.
Description
1 GB2092561A 1
SPECIFICATION
Sintered high density spherical ceramic pellets for gas and oil well proppants and their process of manufacture This invention relates to oil and gas well proppants and more particularly relates to sintered ceramic proppants and a method for maintaining a fracture in a subterreanean formation in a propped condition by utilizing the proppant.
Oil and natural gas are produced from wells having porous and permeable subterranean formation. The porosity of the formation permits the formation to store oil or gas and the 10 permeability of the formation permits the oil or gas fluid to move through the formation. Permeability of the formation is essential to permit oil and gas to flow to a location where it can be pumped from the well. Sometimes, the permeability of the formation holding the gas or oil is insufficient for economic recovery of oil and gas. In other cases during the operation of the well, the permeability of the formation drops to the extent that further recovery becomes uneconomi- 15 cal. In such cases, it is necessary to fracture the formation and prop the fractures in an open condition by means of a proppant material or popping agent. Such fracturing is usually accomplished by hydraulic pressure and the proppant material or propping agent is a particulate material such as sand, glass beads or ceramic particles which are carried into the fracture by means of a fluid.
Spherical particles of uniform size are generally acknowledged to be the most effective proppants due to maximized permeability. For this reason, assuming other properties to be equal, spherical or essentially spherical proppants such as rounded sand grains, metallic shot, glass beads and fused tabular alumina are preferred.
Unfortunately, in deep wells, where high pressures are encountered; e.g., above about 5000 25 psi, the foregoing specifically mentioned proppants are either entirely ineffective or have greatly reduced permeability. The best of the foregoing specifically mentioned proppants at high pressures, as disclosed in U.S. Patent 3,976,138 to Colpoys, Jr. et al, is fused alumina.
However, even fused alumina, as disclosed in U.S. Patent 3,976,138, has dramatically reduced permeability at pressures in excess of 5000 psi.
As disclosed in U.S. Patent 4,068,718 to Cook, Jr. et al, it has recently been discovered that sintered bauxite unexpectedly has a permeability which is superior to the previously mentioned proppant materials at pressures as high as 10,000 psi or higher.
Unfortunately, the sintered bauxite material actually used in making the measurements disclosed in U.S. Patent 4,068,718, does not have the most desired spherical shape for highest 35 permeability since prior to the present invention, it was not possible to commerically manufac ture spherical sintered bauxite particles having a specific gravity in excess of about 3.5 which is required to have sufficient compression strength.
The prior art sintered bauxite particles were elongated pellets which were tumbled to form rounded edges in order to increase permeability. In addition, the yields of such pellets were low 40 compared to the amount of material processed. Rolling the particles prior to sintering, as disclosed in column 4 of U.S. Patent 4,068,718, was entirely ineffective since particles having insufficient density were invariably obtained.
There is therefore provided, in accordance with the present invention, speherical ceramic pellets or particles having densities in excess of 95 percent of the theoretical density of the ceramic material, which spherical particle is useful as an oil and gas well proppant and which may be additionally useful, in certain circumstances, as a lubricant, abrasive, filter media, catalyst support material or bearing material. When the particle is used as a proppant, the ceramic material is preferably sintered bauxite, although other ceramics such as aluminium silicate clays containing aluminium and iron may be used.
The invention further includes a process for propping fractures in oil and gas wells utilizing the particle of the invention by introducing the particle of the invention as a proppant or propping agent into a fluid such as oil or water and introducing the propping agent containing fluid into a fracture in the subterranean fromation containing the well, the compaction pressure upon the fracture being at least 4,000 psi and usually 10,000 psi or higher, said propping 55 agent having an average particle size between 0.1 and 2 millimejers. It has been found that permeability at 4,000 psi or greater is superior to the permeability of prior art essentially spherical sintered bauxite material.
The invention additionally includes a novel efficient process for manufacturing the spherical sintered ceramic pellet in accordance with the invention which comprises adding a sinterable 60 ceramic powder composition, which is most desirably bauxite when the pellet is to be used as a proppant material, having an average particle size of between 0 and about 5 microns to a rotatable table mixer provided with a rotatable impacting impeller which is the same or similar to the one described in U.S. Patent 3,690,622.
The table is rotated from about 10 to about 60 rpm and the impacting impeller is rotated to 65 GB2092561A obtain an impeller tip speed of from about 25 to about 50 meters per second. Sufficient water is added to cause essentially spherical ceramic pellets to form and after such pellets have formed, from about 5 to about 15 percent of additional ceramic powder by weight of pellets is added and the impeller is rotated at a tip speed of between about 5 and about 20 meters per second for from about 1 to about 6 minutes while rotating the table at from about 10 to about 5 rpm.
The resulting pellets are then dried at between about 100 and about 300 degrees centigrade and furnaced at sintering temperature until maximum density is obtained.
The sintered ceramic pellets, in accordance with the invention, have a density in excess of 95 percent of the theoretical density of the ceramic and are spherical in shape, meaning that the 10 average ratio of the minimum diameter to maximum diameter of pellets (sphericity) of repeated random samples of pellets manufactured in accordance with the present invention is greater than 0.82 almost always greater than 0.85 and frequently greater than 0.9 with 95 percent confidence limits.
In contrast, the average ratio of minimum diameter to maximum diameter of extruded and 15 tumbled sintered bauxite pellets in accordance with the prior art is generally less than about
0.80.
"Essentially spherical' as used herein, is intended to mean an average ratio of minimum diameter to maximum diameter of between 0.7 and 0.82.
"Spherical", as used herein, is intended to mean an average ratio of minimum diameter to 20 maximum diameter of greater than 0.82.
The spherical pellets, in accordance with the present invention, are manufactured by sintering a ceramic powder composition. The spherical pellets are not manufactured, as in prior art, by fusion of ceramic material followed by solidification. The ceramic powder may be any sinterable ceramic powder such as powders of bauxite and silicon carbide. If desired, sintering aids may in 25 incorporated as a part of the sinterable ceramic powder. For example, when bauxite is used, bentonite clay or iron oxide aids sintering, when silicon carbide is used, boron, boron carbide, aluminium diboride, boron nitride, boron phosphide and other boron compounds aid sintering and when aluminium silicate type clays are used, fluxes such as iron oxide aid sintering.
Between 0 and 30 weight percent of such sintering aids may be used. The most desirable range 30 of sintering aid can be readily determined by those skilled in the art depending upon the particular ceramic and aid used. For example, from 0 to 8, preferably 0 to 3 percent and most preferably between 0.2 and 1 percent by weight of bentonite aids the sintering of bauxite, from 0.4 to 5 percent of a sintering aid such as a boron containing compound is required for sintering of silicon carbide and up to 30 weight percent of a flux material such as sodium carbonate, lithium carbonate, feldspar, manganese oxide, titania, iron oxide and sodium silicates aid sintering of aluminium silicate clays.
The process comprises adding a sinterable ceramic powder compostion having an average particle size of from between 0 and about 5 microns to a rotatable table mixer provided with a rotatable impacting impeller. The table may be somewhat inclined from the horizontal. The small 40 particle size is required in order to obtain a finished spherical sintered ceramic pellet having sufficient density. A ceramic powder average particle size of even smaller than four microns is desirable and the average particle size is preferably below 3 microns and usually above 0.5 microns.
The rotatable mixer provided with the rotatable impacting impeller can be any such device such as the device obtainable from Eirich Machines Inc. known as the Eirich Mixer. Such a device is provided with a flat or inclined circular table which can be made to rotate at a speed of from about 10 to about 60 revolutions per minute (rpm) and is provided with a rotatable. impacting impeller which can be made to rotate at a tip speed of from about 5 to about 50 meters per second. The central axis of the impacting impeller is generally located within the mixer at a position off center from the central axis of the rotatable table. The table may be in a horizontal or inclined position wherein the incline, if any, is between 0 and 35 degrees from the horizontal. After the sinterable ceramic powder composition is added to the mixer, the table is rotated at from about 10 to about 60 rpm and preferably from about 20 to about 40 rpm and the impacting impeller is rotated to obtain a tip speed of from about 25 to about 50, preferably 25 to about 35, meters per second and sufficient water is added to cause essentially spherical ceramic pellets of the desired size to form. If desired, the impeller may be initially rotated at from about 5 to about 20 meters per second during addition of one-half of the sufficient water and subsequently rotated at the higher tip speed of 25 to about 50 meters per second during the addition of the balance of the water.
In general, the total quantity of water which is sufficient to cause essentially spherical ceramic pellets to form is from about 17 to about 20 percent by weight of the ceramic powder and usually between about 18 and about 20 percent by weight of the ceramic powder. The total mixing time after addition of an initial quantity of the sufficient water to the formation of essentially spherical pellets of the desired size is from about 2 to about 6 minutes.
A 1 4i 3 GB2092561A 3 From about 5 to about 15 percent and preferably from about 8 to about 10 percent of additional ceramic powder by weight of pellets is then added, followed by rotating the impeller at a tip speed of between about 5 and about 20 meters per second, preferably between about and about 20 meters per second for from about 1 to about 6 minutes while continuing to rotate the table at from about 10 to about 60 rpm and preferably from about 20 to about 40 5 rpm.
If desired, the rotation of the impeller may then be stopped while the table continues to rotate for between about 1 and about 5 minutes.
The impacting impeller is preferably a disc provided with peripheral rods or bars attached to the disc. The longitudinal axis of the rods or bars is desirably essentially parallel with the axis of 10 rotation of the impeller, which is usually a vertical axis. The diameter of the impeller is measured from the axis of rotation to the center of the most distant rod or bar. Tip speed is the speed of the most distant rod or bar.
The diameter of the impeller depends upon the size of the mixer but is usually less than 25 percent of the diameter of the mixer. The impeller in most applications is between 10 and 100 15 centimeters in diameter and usually rotates at from 200 to 3750 rpm at the lower tip speeds of to 20 meters per second depending upon impeller diameter and at from 500 to 6500 rpm at the higher tip speeds of 25 to 35 meters per second depending upon impeller diameter.
The mixer may also be provided with a deflector plate to deflect ceramic material from the mixer wall and preferably to the impeller.
The resulting pellets are dried at a temperature of between about 100 and about 300C until preferably less than 3 percent and most preferably less than 1 percent moisture remains in the pellets. The most preferred drying temperature is between about 175 and 275'C and the drying time usually between about 30 and about 60 minutes. The pellets are then furnaced at sintering temperature until maximum density is obtained. In the case of bauxite having less than about 25 percent alumina with substantial quantities of Fe2031 Si02 and Ti02, the furnacing usually occurs at a temperature of between about 1,450C and 1,550'C for from about 1 to about 10 minutes and preferably occurs at from about 1,485C to about 1,51 5'C for from about 2 to about 4 minutes.
The density which is obtained is in excess of about 95 percent of the theoretical density of the 30 ceramic material used. The theoretical density of bauxite varies somewhat due to the somewhat different bauxite compositions occurring in nature; however, the theorectical density of bauxite is usually about 3.72 and the maximum density obtained as a result of the process of the invention exceeds 3.57 and usually is between about 3.60 and 3.68. Since tumbling for 10 minutes to 1 hour substantially enhances such smoothness, the finished pellets can be tumbled 35 if desired.
When the pellets are used as a propping agent for increasing permeability in a subterranean earth formation penetrated by a well, the spherical pellets are introduced into a fluid and the fluid containing the propping agent is introduced into a fracture which has a compaction pressure of at least 4,000 psi, to deposit a propping distribution of the propping agent in the 40 fracture. The propping distribution is usually, but not necessarily, a multilayer pack and the overall particle size of the propping agent is between 0.1 and 2 millimeters.
The following examples serve to illustrate and not limit the invention. Unless otherwise indicated, parts and percentages are by weight.
EXAMPLE 1.
About 135 kilograms of Surinam bauxite powder having an average particle size of less than 4 microns were added with about 1.35 kilograms of bentonite clay powder to an Brick mixer having a pan diameter of about 115 centimeters, an operating capacity of about 160 kilograms and an impacting impeller diameter of about 27 centimeters.
The pan was rotated at about 35 rpm and the impeller was rotated at about 1090 rpm and about 82 kilograms of water was added. Rotation of the pan and impeller continued for about 1 minute followed by increasing the impeller speed to about 2175 rpm and an additional 82 kilograms of water was added. The pan and impeller continue to rotate until seed pellets are formed which contain less than 5 percent pellets of a size smaller than 35 mesh. (about 3 minutes) The impeller is then reduced to about 1090 rpm and about 9 pounds of the foregoing bauxite powder containing 0.5 percent bentonite clay is added. Rotation of the pan and impeller then continues for an additional 2 minutes to form spherical pellets.
The pellets are then dried for about 30 minutes at about 225C in a rotating tray dryer and are then fired at about 1 500'C for about 3 minutes. The yield of useful pellets having a size 60 between 14 and 60 grit is greater than 90 percent. The resulting pellets have a density of about 3.64 and a sphericity of about 0.9.
EXAMPLE 2 About 450 kilograms of Surinan bauxite powder having an average particle size of less than 4 65 4 GB2092561A microns were blended with about 4.5 kilograms of Bentonite clay and about 164 kilograms of water in a mix muller. The resulting putty-like material is then extruded through an eight inch extruder at room temperature with a water cooled barrel. The die size corresponds to the diameter of a 10 to 12 grit particle. The resulting extruded material is dried for one hour at 260C and granulation is accomplished in a Stokes reciprocating granulator followed by a four minute pass through a Blunger. Dust is removed by sifting and rounded shapes are generated by tumbling. The resulting pellets are sintered as in Example 1.
The yield of useful pellets having a size between 14 and 60 grit is less than 80 percent. The resulting pellets have a density of about 3.64 and have a sphericity of less than about 0.8.
EXAMPLE 3
Bauxite powder containing 3 weight percent bentonite was pelletized by rolling in a FerroTech pelletizer and fired in a rotary kiln at 1 525C for 3 minutes. 1 525C in a rotary kiln was insufficient for densification as indicated by the white colour.
Pellets were then fired at a gas kiln for one hour at 1 525C. This firing treatment resulted in 15 apparent specific gravity of 3.30.
EXAMPLE 4 The permeability in darcies of the pellets manufactured in accordance with Example 1 was compared with the permeability in darcies of the pellets manufactured in accordance with Example 2 in 2% KCL solution at 200'F at various applied pressures. The results are shown in Table A.
i TABLE A
Pressure Permeability psi Example 1 Permeability Example 2 2000 285 304 4000 274 251 30 6000 248 242 8000 233 222 10000 222 213 35 This example clearly shows that the pellets in accordance with the invention show between about 4 and above 9% better flow at pressures of 4000 psi to 10,000 psi.
EXAMPLE 5
The pellets of Example 1 were compared for compresibility with the pellets of Example 2 at 40 16,000 psi under a piston in a confined tube. A bed of about 0.25 inch of the pellets of the invention in the test showed a compressibility of between 40 and 56 thousandths of an inch; whereas, the pellets of Example 2 under the same conditions and thickness showed a compressibility of between 52 and 60 thousandths of an inch.
Claims (7)
- CLAIMS 1. Spherical sintered ceramic pellets having a density in excess of95% of the maximum theoretical density of the ceramic wherein repeated random samples of such pellets indicate an average sphericity of greater than 0.82 with 95% confidence limits. 50
- 2. Spherical sintered bauxite pellets having a density in excess of about
- 3.57 grams per cubic centimeter wherein repeated random samples of such pellets random samples of such pellets indicate an average sphericity of greater than 0.82 with 95% confidence limits. 3. Spherical sintered ceramic pellets in accordance with claim 1 wherein repeated random samples of such pellets indicates an average sphericity of greater than 0.85 with 95% confidence limits.
- 4. Spherical sintered ceramic pellets in accordance with claim 3 wherein repeated random samples of such pellets indicates an average sphericity of greater than 0.9 limits.
- 5. Spherical sintered bauxite pellets in accordance with claim 2 wherein repeated random samples of such pellets indicates an average sphericity of greater than 0. 85 with 95% confidence limits.
- 6. Spherical sintered bauxite pellets in accordance with claim 5 wherein repeated random samples of such pellets indicates an average sphericity of greater than 0.9 with 95% confidence limits.
- 7.Spherical sintered ceramic pellets substantially as hereinbefore described.with 95% confidence GB2092561A 5 Printed for Her Majesty's Stationery Office by Burgess & Son (Abingdon) Ltd-1 982. Published at The Patent Office, 25 Southampton Buildings, London, WC2A 1AY, from which copies may be obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US96912278A | 1978-12-13 | 1978-12-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2092561A true GB2092561A (en) | 1982-08-18 |
GB2092561B GB2092561B (en) | 1983-10-05 |
Family
ID=25515210
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7940365A Expired GB2037727B (en) | 1978-12-13 | 1979-11-22 | Sintered spherical ceramic pellets for gas and oil well proppants |
GB8205575A Expired GB2092561B (en) | 1978-12-13 | 1979-11-22 | Slintered high density spherical ceramic pellets |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7940365A Expired GB2037727B (en) | 1978-12-13 | 1979-11-22 | Sintered spherical ceramic pellets for gas and oil well proppants |
Country Status (4)
Country | Link |
---|---|
CA (1) | CA1117987A (en) |
DE (1) | DE2948584A1 (en) |
FR (1) | FR2450245A1 (en) |
GB (2) | GB2037727B (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0116369A2 (en) * | 1983-02-07 | 1984-08-22 | Norton Company | Proppant for fractured wells |
AU628700B2 (en) * | 1989-12-22 | 1992-09-17 | Comalco Aluminium Limited | Ceramic microspheres |
US7036591B2 (en) | 2002-10-10 | 2006-05-02 | Carbo Ceramics Inc. | Low density proppant |
US7825053B2 (en) | 2004-09-14 | 2010-11-02 | Carbo Ceramics Inc. | Sintered spherical pellets |
EP3155064A4 (en) * | 2014-06-13 | 2018-03-07 | Imerys Oilfield Minerals, Inc. | Method of making proppants and anti-flowback additives using gear pelletizers |
EP2407525B1 (en) * | 2006-09-01 | 2018-10-10 | Imerys | Rod-shaped proppants and anti-flowback additives comprising Aluminium Titanate |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2079261B (en) * | 1980-07-07 | 1983-06-08 | Niro Atomizer As | Process for the production of sintered bauxite spheres |
US4440866A (en) * | 1980-07-07 | 1984-04-03 | A/S Niro Atomizer | Process for the production of sintered bauxite spheres |
US4518039A (en) * | 1981-08-20 | 1985-05-21 | Graham John W | Method for treating subterranean formations |
CH667223A5 (en) * | 1981-12-23 | 1988-09-30 | Alusuisse | METHOD AND DEVICE FOR ROUNDING DOWN GRANULAR SOLID PARTICLES. |
US4522731A (en) * | 1982-10-28 | 1985-06-11 | Dresser Industries, Inc. | Hydraulic fracturing propping agent |
US4658899A (en) * | 1982-02-09 | 1987-04-21 | Standard Oil Proppants Company, L.P. | Use of uncalcined/partially calcined ingredients in the manufacture of sintered pellets useful for gas and oil well proppants |
US4623630A (en) | 1982-02-09 | 1986-11-18 | Standard Oil Proppants Company | Use of uncalcined/partially calcined ingredients in the manufacture of sintered pellets useful for gas and oil well proppants |
US4427068A (en) * | 1982-02-09 | 1984-01-24 | Kennecott Corporation | Sintered spherical pellets containing clay as a major component useful for gas and oil well proppants |
DE3223024A1 (en) * | 1982-06-19 | 1983-12-22 | Battelle-Institut E.V., 6000 Frankfurt | METHOD FOR PRODUCING A SUPPORT |
US5120455A (en) * | 1982-10-28 | 1992-06-09 | Carbo Ceramics Inc. | Hydraulic fracturing propping agent |
US4537254A (en) * | 1983-01-03 | 1985-08-27 | Chevron Research Company | Steam injection well gravel pack material of sintered bauxite |
US4548269A (en) * | 1983-01-03 | 1985-10-22 | Chevron Research Company | Steam injection well gravel prepack material of sintered bauxite |
US4555493A (en) * | 1983-12-07 | 1985-11-26 | Reynolds Metals Company | Aluminosilicate ceramic proppant for gas and oil well fracturing and method of forming same |
US4680230A (en) * | 1984-01-18 | 1987-07-14 | Minnesota Mining And Manufacturing Company | Particulate ceramic useful as a proppant |
US4944905A (en) * | 1984-01-18 | 1990-07-31 | Minnesota Mining And Manufacturing Company | Particulate ceramic useful as a proppant |
US4668645A (en) * | 1984-07-05 | 1987-05-26 | Arup Khaund | Sintered low density gas and oil well proppants from a low cost unblended clay material of selected composition |
CA1228226A (en) * | 1984-07-05 | 1987-10-20 | Arup K. Khaund | Sintered low density gas and oil well proppants from a low cost unblended clay material of selected compositions |
US4713203A (en) * | 1985-05-23 | 1987-12-15 | Comalco Aluminium Limited | Bauxite proppant |
US4632876A (en) * | 1985-06-12 | 1986-12-30 | Minnesota Mining And Manufacturing Company | Ceramic spheroids having low density and high crush resistance |
BR0301036B1 (en) | 2003-04-29 | 2013-09-10 | suitable for hydraulic fracturing of oil or gas wells as well as method for reducing or eliminating the flow reversal phenomenon in oil or gas wells | |
AU2006218614A1 (en) | 2005-03-01 | 2006-09-08 | Carbo Ceramics Inc. | Methods for producing sintered particles from a slurry of an alumina-containing raw material |
DE102005045180B4 (en) | 2005-09-21 | 2007-11-15 | Center For Abrasives And Refractories Research & Development C.A.R.R.D. Gmbh | Spherical corundum grains based on molten aluminum oxide and a process for their preparation |
US7828998B2 (en) | 2006-07-11 | 2010-11-09 | Carbo Ceramics, Inc. | Material having a controlled microstructure, core-shell macrostructure, and method for its fabrication |
CN101563525A (en) | 2006-08-30 | 2009-10-21 | 卡博陶粒有限公司 | Low bulk density proppant and methods for producing the same |
RU2344156C2 (en) * | 2007-02-28 | 2009-01-20 | Шлюмбергер Текнолоджи Б.В. | Proppant and method of well efficiency increase |
WO2009009370A1 (en) | 2007-07-06 | 2009-01-15 | Carbo Ceramics Inc. | Proppants for gel clean-up |
DE102010007176A1 (en) * | 2010-02-08 | 2011-08-11 | Polysius AG, 59269 | Method for producing a refractory material from bauxite |
US9227874B2 (en) | 2011-01-25 | 2016-01-05 | Halliburton Energy Services, Inc. | Extrusion process for proppant production |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3437148A (en) * | 1967-01-06 | 1969-04-08 | Union Carbide Corp | Method and article for increasing the permeability of earth formations |
DE1592088A1 (en) * | 1967-06-01 | 1970-12-03 | Dynamit Nobel Ag | Process for the production of pressure- and abrasion-resistant balls |
US3890072A (en) * | 1973-09-04 | 1975-06-17 | Norton Co | Apparatus for forming solid spherical pellets |
CA1045027A (en) * | 1975-09-26 | 1978-12-26 | Walter A. Hedden | Hydraulic fracturing method using sintered bauxite propping agent |
-
1979
- 1979-11-06 CA CA000339222A patent/CA1117987A/en not_active Expired
- 1979-11-22 GB GB7940365A patent/GB2037727B/en not_active Expired
- 1979-11-22 GB GB8205575A patent/GB2092561B/en not_active Expired
- 1979-11-23 FR FR7928939A patent/FR2450245A1/en active Pending
- 1979-12-03 DE DE19792948584 patent/DE2948584A1/en not_active Withdrawn
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0116369A2 (en) * | 1983-02-07 | 1984-08-22 | Norton Company | Proppant for fractured wells |
EP0116369A3 (en) * | 1983-02-07 | 1985-07-03 | Norton Company | Proppant for fractured wells |
AU628700B2 (en) * | 1989-12-22 | 1992-09-17 | Comalco Aluminium Limited | Ceramic microspheres |
US7036591B2 (en) | 2002-10-10 | 2006-05-02 | Carbo Ceramics Inc. | Low density proppant |
US7825053B2 (en) | 2004-09-14 | 2010-11-02 | Carbo Ceramics Inc. | Sintered spherical pellets |
EP2407525B1 (en) * | 2006-09-01 | 2018-10-10 | Imerys | Rod-shaped proppants and anti-flowback additives comprising Aluminium Titanate |
EP2500395B1 (en) * | 2006-09-01 | 2018-10-10 | Imerys | Method of manufacturing rod-shaped proppants and anti-flowback additives comprising aluminium titanate |
EP3155064A4 (en) * | 2014-06-13 | 2018-03-07 | Imerys Oilfield Minerals, Inc. | Method of making proppants and anti-flowback additives using gear pelletizers |
Also Published As
Publication number | Publication date |
---|---|
GB2037727B (en) | 1983-05-05 |
FR2450245A1 (en) | 1980-09-26 |
GB2092561B (en) | 1983-10-05 |
DE2948584A1 (en) | 1980-06-26 |
GB2037727A (en) | 1980-07-16 |
CA1117987A (en) | 1982-02-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19971122 |