US3494949A - Aluminum salts of alkyl orthophosphates - Google Patents

Aluminum salts of alkyl orthophosphates Download PDF

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US3494949A
US3494949A US606578A US3494949DA US3494949A US 3494949 A US3494949 A US 3494949A US 606578 A US606578 A US 606578A US 3494949D A US3494949D A US 3494949DA US 3494949 A US3494949 A US 3494949A
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oil
aluminum
viscosity
oleyl
orthophosphates
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US606578A
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Roger F Monroe
Bob E Rooker
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Dow Chemical Co
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Dow Chemical Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/08Esters of oxyacids of phosphorus
    • C07F9/09Esters of phosphoric acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L7/00Fuels produced by solidifying fluid fuels
    • C10L7/02Fuels produced by solidifying fluid fuels liquid fuels
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/042Metal salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2070/00Specific manufacturing methods for lubricant compositions
    • C10N2070/02Concentrating of additives

Definitions

  • the viscosity-temperature relationship of a hydrocarbon fluid is one of its more important characteristics in that it is this relationship which is indicative of the relative change in viscosity with temperature.
  • the oil in motor oils of the type known as crankcase oils, it is desirable for the oil to have a viscosity that is sufficiently high at an elevated temperature to provide adequate lubrication and to prevent excessive oil consumption.
  • the motor oil should have a viscosity sufficiently low at atmospheric temperature to provide ease of engine starting. Increasing the high temperature viscosity of an oil while decreasing its low temperature viscosity can be accomplished only by improving the viscosity-temperature relationship, or stated differently, by raising the viscosity index of the oil.
  • aluminum soaps are presently being used as thickeners for gasoline, kerosene, and petroleum oils.
  • the soaps have to be prepared in situ and the gelled gasoline, kerosene or petroleum oil is not stable to extended'periods of storage or to heat.
  • the lubricating oil to which the viscosity index improving agent is added according to the invention is preferably and advantageously a highly refined parafiinic oil.
  • highly refined parafiinic oil we mean a petroleum lubricating oil which has been refined by one of the more drastic refining methods known in the art, for example, by conventional aluminum chloride refining or by solvent extraction adapted to remove all or substantially all of the unsaturated and naphthenic constituents of the oil.
  • Aluminum chloride refined or solvent extracted parafiinic base oil such as a Pennsylvania oil, provides an excellent base oil for the composition of the invention. However, drastically refined Mid-Continent and Gulf Coastal oil may also be used.
  • Organic phosphates that form suitable aluminum salts for the purposes of this invention are bis-hexadecyl, n-butyl, n-dodecyl, n-butyl, n-hexadecyl, isobutyl dodecyl, ethyl n-dodecyl and the C to C alkyl oleyl orthophosphates.
  • Aluminum ethyl oleyl orthophosphate has been found to be particularly advantageous for improving the viscosity of the lubricating oils and for gelling gasoline.
  • the aluminum o-phosphate ester products can be employed per se or they can be added to the fluid in the form of a concentrate.
  • the aluminum product can be prepared in an organic solvent which can be flashed from the oil after formation of the concentrate.
  • Organic solvents suitable for this purpose include hexane, isooctane, naphtha, benzene, toluene, and the like.
  • the concentrate can be added directly to the oil to be improved or it can be admixed with one or more other improving agents. Regardless of whether products are employed per se or in the form of a mineral oil concentrate, an amount is used suflicient to improve the viscosity index and/or pour point of the oil.
  • the products are useful when employed in amounts of about 0.1 to about 5 percent by weight. Amounts in excess of 5 percent are generally undesirable because the oil becomes too viscous for satisfactory use as crankcase lubricant. Excellent results have been obtained by the use in petroleum distillates, such as SAE 10 and SAE 25 lubricating oil, of amounts of the products between 0.1 and 0.5 percent by weight of the composition. It will be understood that the optimum amount will vary according to the particular mineral oil and according to the conditions to which the oil is subjected.
  • the lubricating oil composition of this invention can contains other addition agents normally added to lubricating oils for a specific purpose such as an oiliness and extreme pressure agent, an anti-oxidant, a corrosion inhibitor, a foam suppressant, a dye, a sludge inhibitor, and the like.
  • Aluminum alkyl orthophosphates when dissolved in gasoline, kerosene or other hydrocarbon fluid, in concentrations from 0.15% will cause them to gel.
  • Gelled gasoline or kerosene can be stored for extended periods of time and is stable to heat.
  • the degree of gelling can be controlled by the concentration of the orthophosphate salt in the fluid. For example, a one percent solution of aluminum ethyl oleyl orthophosphate in gasoline will flow like molasses and has good adhesion properties, whereas the present thickeners used for napalm bombs will not flow and have poor adhesion properties.
  • the gelled hydrocarbons can be thinned by the addition of more hydrocarbons. Also a mixture of hydrocarbons can be gelled i.e.-gasoline, kerosene and petroleum oil.
  • Example I.-Preparation of aluminum ethyl oleyl orthophosphate Into a two liter flask equipped with a mechanical stirrer, a dropping funnel and a thermometer are placed 178 gms. of ethyl oleyl orthophosphate, 400 ml. of water and 250 ml. of 95% ethanol. To this mixture is added 19 gms. of sodium hydroxide in 200 ml. of water. The temperature of the reaction mixture is maintained at C. while 68 gms. of aluminum sulfate 18 H O in 200 ml. of water is added slowly with rapid stirring. A finely dispersed precipitate is formed, which is filtered and left wet. The decomposition point of the solid was 237 C.
  • Example II Preparation of aluminum ethyl oleyl orthophosphate in situ in kerosene
  • the concentrate is prepared by adding 752 gms. (2 mols.) of ethyl oleyl phosphoric acid to 5248 gms. of
  • Example IV Preparation of N-butyl dodecyl phosphoric acid Into a 2-liter, 3-necked round bottom flask, equipped with a stirrer, reflux condenser, dropping funnel, thermometer, and means for cooling, there were charged 400 mls. of n-hexane. Then, 142 grams (1 mol.) of phosphorus pentoxide (P 0 were gradually added to the hexane with stirring to form a slurry.
  • P 0 phosphorus pentoxide
  • reaction mixture was gradually heated to 66 C., the reflux temperature of hexane, and held there for one hour to complete the reaction.
  • the hexane solvent was removed by distillation under reduced pressure.
  • the recovered dialkyl phosphoric acid is a white grease with melting point of 30-33 C. and a refractive index at 25 C. of 1.4446.
  • the aluminum salt of the above product is readily formed by the methods shown in the above examples.
  • Example V Following the procedure and using the test oil of Example III, the indicated aluminum orthophosphates, which were prepared by the same procedure illustrated in Example IV, were tested at the concentrations and with the results set out in the table.
  • Patent 2,983,679 the following experiments were run employing Amoco Test Oil SUS-l (SAE) having a kinematic viscosity
  • SAE Amoco Test Oil SUS-l
  • the elfect of the novel compounds of this invention in depressing the pour point of hydrocarbon fiuids was determined by placing an 8 02. round bottle, which was half-filled with the fluid containing a minor proportion of the desired additive, in a deep freeze at 5 F. for a specified time, removing the bottle, laying it horizontal and recording the time it takes the fluid to move one inch.
  • Amoco Test Oil SUS- with no additive does not move in 60 seconds after 24 hours at 5 F.
  • When containing 0.19 weight percent of aluminum ethyl oleyl orthophosphate the oil moved the one inch in 4.8 seconds after standing for 60 hours at 5 F. Similar results are obtained when employing other novel compounds of this invention.

Description

United States Patent Office 3,494,949 Patented Feb. 10, 1970 ABSTRACT OF THE DISCLOSURE This invention relates to certain novel aluminum salts of alkyl-orthophosphates and to hyrocarbon fluid compositions containing such salts, which compositions have improved viscosity characteristics.
BACKGROUND OF THE INVENTION Field of the invention The viscosity-temperature relationship of a hydrocarbon fluid is one of its more important characteristics in that it is this relationship which is indicative of the relative change in viscosity with temperature. Thus, in motor oils of the type known as crankcase oils, it is desirable for the oil to have a viscosity that is sufficiently high at an elevated temperature to provide adequate lubrication and to prevent excessive oil consumption. On the other hand, the motor oil should have a viscosity sufficiently low at atmospheric temperature to provide ease of engine starting. Increasing the high temperature viscosity of an oil while decreasing its low temperature viscosity can be accomplished only by improving the viscosity-temperature relationship, or stated differently, by raising the viscosity index of the oil.
Description of the prior art In order to reduce excessive change in viscosity with temperature, various viscosity index improvers have been developed. In the past, for example, polymerized esters of the acrylic series have been used to improve the viscosity-temperature relationship of mineral oils but these esters have not been entirely satisfactory inasmuch as their viscosity index improving characteristics is lost or substantially reduced when the oil in which they are incorporated is subjected to vigorous agitation and high shear rates and stresses. It is believed that the lowering of the viscosity index of an oil containing a long chain polymer as a viscosity index improving agent is a result of such polymer being split into polymers of shorter chain length by the shearing stress, the shorter chain polymers being less effective as viscosity index improvers.
In addition, aluminum soaps are presently being used as thickeners for gasoline, kerosene, and petroleum oils. The soaps have to be prepared in situ and the gelled gasoline, kerosene or petroleum oil is not stable to extended'periods of storage or to heat.
SUMMARY OF THE INVENTION We have found that certain aluminum salts of alkyl orthophosphates gel hydrocarbon fluids and impart excellent, viscosity index characteristics to a mineral oil, and that the oil thus improved retains its high viscosity index even when subjected to vigorous agitation and high shear rates and stresses. We have found further that a lubricating composition comprising a major amount of a lubricating oil and a minor amount of these aluminum salts of alkyl orthophosphates has a greatly improved pour point.
The lubricating oil to which the viscosity index improving agent is added according to the invention is preferably and advantageously a highly refined parafiinic oil. By the term highly refined parafiinic oil we mean a petroleum lubricating oil which has been refined by one of the more drastic refining methods known in the art, for example, by conventional aluminum chloride refining or by solvent extraction adapted to remove all or substantially all of the unsaturated and naphthenic constituents of the oil. Aluminum chloride refined or solvent extracted parafiinic base oil, such as a Pennsylvania oil, provides an excellent base oil for the composition of the invention. However, drastically refined Mid-Continent and Gulf Coastal oil may also be used. While the highly refined paraffinic oils are particularly desirable for use in forming crankcase lubricants, we do not wish to limit the invention to these oils alone, inasmuch as the aluminum alkyl orthophosphates are also useful in improving the viscosity index and/or pour point of oils derived from naphthenic and asphaltic crudes.
Organic phosphates that form suitable aluminum salts for the purposes of this invention are bis-hexadecyl, n-butyl, n-dodecyl, n-butyl, n-hexadecyl, isobutyl dodecyl, ethyl n-dodecyl and the C to C alkyl oleyl orthophosphates. Aluminum ethyl oleyl orthophosphate has been found to be particularly advantageous for improving the viscosity of the lubricating oils and for gelling gasoline.
The aluminum o-phosphate ester products can be employed per se or they can be added to the fluid in the form of a concentrate. In preparing a mineral oil concentrate, the aluminum product can be prepared in an organic solvent which can be flashed from the oil after formation of the concentrate. Organic solvents suitable for this purpose include hexane, isooctane, naphtha, benzene, toluene, and the like. When a mineral oil concentrate is prepared first, the concentrate can be added directly to the oil to be improved or it can be admixed with one or more other improving agents. Regardless of whether products are employed per se or in the form of a mineral oil concentrate, an amount is used suflicient to improve the viscosity index and/or pour point of the oil. For example, the products are useful when employed in amounts of about 0.1 to about 5 percent by weight. Amounts in excess of 5 percent are generally undesirable because the oil becomes too viscous for satisfactory use as crankcase lubricant. Excellent results have been obtained by the use in petroleum distillates, such as SAE 10 and SAE 25 lubricating oil, of amounts of the products between 0.1 and 0.5 percent by weight of the composition. It will be understood that the optimum amount will vary according to the particular mineral oil and according to the conditions to which the oil is subjected.
The lubricating oil composition of this invention can contains other addition agents normally added to lubricating oils for a specific purpose such as an oiliness and extreme pressure agent, an anti-oxidant, a corrosion inhibitor, a foam suppressant, a dye, a sludge inhibitor, and the like.
Aluminum alkyl orthophosphates when dissolved in gasoline, kerosene or other hydrocarbon fluid, in concentrations from 0.15% will cause them to gel. Gelled gasoline or kerosene can be stored for extended periods of time and is stable to heat. The degree of gelling can be controlled by the concentration of the orthophosphate salt in the fluid. For example, a one percent solution of aluminum ethyl oleyl orthophosphate in gasoline will flow like molasses and has good adhesion properties, whereas the present thickeners used for napalm bombs will not flow and have poor adhesion properties.
The gelled hydrocarbons can be thinned by the addition of more hydrocarbons. Also a mixture of hydrocarbons can be gelled i.e.-gasoline, kerosene and petroleum oil.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Example I.-Preparation of aluminum ethyl oleyl orthophosphate :Into a two liter flask equipped with a mechanical stirrer, a dropping funnel and a thermometer are placed 178 gms. of ethyl oleyl orthophosphate, 400 ml. of water and 250 ml. of 95% ethanol. To this mixture is added 19 gms. of sodium hydroxide in 200 ml. of water. The temperature of the reaction mixture is maintained at C. while 68 gms. of aluminum sulfate 18 H O in 200 ml. of water is added slowly with rapid stirring. A finely dispersed precipitate is formed, which is filtered and left wet. The decomposition point of the solid was 237 C.
When one gram (dry weight) of wet aluminum ethyl oleyl orthophosphate is dissolved in 100 ml. of gasoline, a gel is formed. Heat and agitation greatly hastens the gelling of gasoline. The degree of thickening will be determined by the concentration of the additive in gasoline.
Example II.Preparation of aluminum ethyl oleyl orthophosphate in situ in kerosene The concentrate is prepared by adding 752 gms. (2 mols.) of ethyl oleyl phosphoric acid to 5248 gms. of
4 (cs.) at 210 F. of 5.5 and at 100 F. of 35.5. In each case the concentration of additive was 0.2%.
Kinematic viscosity (cs.)
Example IV.Preparation of N-butyl dodecyl phosphoric acid Into a 2-liter, 3-necked round bottom flask, equipped with a stirrer, reflux condenser, dropping funnel, thermometer, and means for cooling, there were charged 400 mls. of n-hexane. Then, 142 grams (1 mol.) of phosphorus pentoxide (P 0 were gradually added to the hexane with stirring to form a slurry.
In the meantime, 372 grams (2 mols) of dodecyl alcohol and 148 gms. (2 mols) of n-butyl alcohol were mixed together to form an equimolecular admixture.
Then the above mixture of alcohols was added slowly to the hexane-phosphorus pentoxide slurry with stirring, keeping the temperature below C. with cooling, the reaction being very exothermic.
After all the alcohol had been added, the reaction mixture was gradually heated to 66 C., the reflux temperature of hexane, and held there for one hour to complete the reaction.
The hexane solvent was removed by distillation under reduced pressure. The recovered dialkyl phosphoric acid is a white grease with melting point of 30-33 C. and a refractive index at 25 C. of 1.4446.
The aluminum salt of the above product is readily formed by the methods shown in the above examples.
Example V Following the procedure and using the test oil of Example III, the indicated aluminum orthophosphates, which were prepared by the same procedure illustrated in Example IV, were tested at the concentrations and with the results set out in the table.
TABLE Decompo- Kinematic Viscosity (es.)
sition Cone, Aluminum orthophosphate point, 0. Physical appearance wt. percent 210 F. 100 F. V.I.
Bis hexadecyl 233 Light tan solid .66 10.02 58. 12 171 Ethyl dodecyL. 255 White, waxy solid 166 12. 2 91. 155 n-Butyl dodeeyL. 219 d0 5 23.09 153. 74 100 n-Butyl hexadecyl 256 White solid G6 28. 58 166 141. 5 iso-Butyl dodecyl 250 White, waxy solid 6G 6. 7 42.52 121 Oetyl oleyl 226 Cream colored rubbery solid 1 6. 25 47. 24 84 Hexyl oleyl. 192 .do 1 6. 38 45. 38 07 Methyl oleyl. 245 Yellow grease 1 6. 02 40. 18 103 n-Propyl oleyl 245 Cream colored rubbery solid. 1 6. 51 45. 3 103 iso-Propyl oleyl. 238 Yellow grease 1 5. s9 38. 82 103 n-Butyl oleyl 248 Cream colored rubbery solid 1 6. 86 46.19 114 Example 111 To illustrate the results obtained when employing aluminum ethyl oleyl orthophosphate in comparison with the results obtained when employing a corresponding rare earth compound such as taught in US. Patent 2,983,679, the following experiments were run employing Amoco Test Oil SUS-l (SAE) having a kinematic viscosity The elfect of the novel compounds of this invention in depressing the pour point of hydrocarbon fiuids was determined by placing an 8 02. round bottle, which was half-filled with the fluid containing a minor proportion of the desired additive, in a deep freeze at 5 F. for a specified time, removing the bottle, laying it horizontal and recording the time it takes the fluid to move one inch. Amoco Test Oil SUS- with no additive does not move in 60 seconds after 24 hours at 5 F. When containing 0.19 weight percent of aluminum ethyl oleyl orthophosphate the oil moved the one inch in 4.8 seconds after standing for 60 hours at 5 F. Similar results are obtained when employing other novel compounds of this invention.
We claim:
References Cited UNITED STATES PATENTS Farrington et al. 25235 Farrington et a1. 260-448 XR Denison et al. 252--38 Denison et al. 25232 6 Farrington et al. 260--448 Ziegler. Heyden 260448 XR Hartle 260-448 XR Mack et al. 260-435 Johnson 260-448 DELBERT E. GANTZ, Primary Examiner 0 H. M. S. SNEED, Assistant Examiner US. Cl. X.R.
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Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3757864A (en) * 1971-05-12 1973-09-11 Dow Chemical Co Friction reducing and gelling agent for organic liquids
US3877972A (en) * 1971-08-11 1975-04-15 Dow Chemical Co Method for coating interior oven surfaces to provide easy soil removal
US4003393A (en) * 1973-02-14 1977-01-18 The Dow Chemical Company Gel-like composition for use as a pig in a pipeline
US4038207A (en) * 1975-11-03 1977-07-26 Borg-Warner Corporation Stabilized hydrocarbon gels and a method for their preparation
US4115285A (en) * 1977-06-13 1978-09-19 Borg-Warner Corporation Cutting oil additives
US4152289A (en) * 1976-02-06 1979-05-01 The Dow Chemical Company Gelling of organic liquids
US4153649A (en) * 1976-02-09 1979-05-08 The Dow Chemical Company Phosphate ester-type reaction product and method of preparing same
US4163018A (en) * 1976-12-18 1979-07-31 Sakai Chemical Industry Company, Ltd. Process for preparing metal salts of alkyl phosphates
US4174283A (en) * 1976-02-06 1979-11-13 The Dow Chemical Company Method of fracturing with gelled organic liquids
US4770814A (en) * 1983-08-31 1988-09-13 The Dow Chemical Company Shear stable antimisting formulations
US4787994A (en) * 1988-04-11 1988-11-29 Petrolite Corporation Method for preparation of hydrocarbon fracturing fluids, fluids prepared thereby, and methods related thereto
US4880565A (en) * 1983-08-31 1989-11-14 The Dow Chemical Company Fluorine containing viscoelastic surfactants
US5057233A (en) * 1988-01-11 1991-10-15 Nalco Chemical Company Hydrocarbon geller and method for making the same
US5110485A (en) * 1990-07-16 1992-05-05 Nalco Chemical Company Liquid aluminum phosphate salt gelling agent
US5202035A (en) * 1990-07-16 1993-04-13 Nalco Chemical Company Liquid aluminum phosphate salt gelling agent
US5514645A (en) * 1992-01-07 1996-05-07 Halliburton Company Method of gelling hydrocarbons and fracturing subterranean formations
US6149693A (en) * 1996-02-06 2000-11-21 Ethox Chemicals, Inc. Hydrocarbon gels useful in formation fracturing
US6184405B1 (en) * 1996-11-04 2001-02-06 Ticona Gmbh Process for preparing aluminum salts of organic phosphoric acids
US6261998B1 (en) * 1998-05-12 2001-07-17 Fracmaster Ltd. Refined oil gelling system
US20030228985A1 (en) * 2001-02-23 2003-12-11 Taylor Robert S. Methods and compositions for treating subterranean formations with gelled hydrocarbon fluids
US20040214728A1 (en) * 2001-02-23 2004-10-28 Taylor Robert S. Methods and compositions for treating subterranean formations with gelled hydrocarbon fluids
US20050250652A1 (en) * 2004-05-05 2005-11-10 Taylor Robert S Gelled invert emulsion compositions and methods of use and manufacture
US20110136705A1 (en) * 2009-12-04 2011-06-09 Elementis Specialties, Inc. Phosphate ester oil gellant
US20110184082A1 (en) * 2010-01-27 2011-07-28 Kraton Polymers U.S. Llc Compositions Containing Styrene-Isobutylene-Styrene And Styrene-Ethylene/Butylene-Styrene Block Copolymers
US8119575B2 (en) 2001-02-23 2012-02-21 Halliburton Energy Services, Inc. Methods and compositions for treating subterranean formations with gelled hydrocarbon fluids

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Cited By (31)

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Publication number Priority date Publication date Assignee Title
US3757864A (en) * 1971-05-12 1973-09-11 Dow Chemical Co Friction reducing and gelling agent for organic liquids
US3877972A (en) * 1971-08-11 1975-04-15 Dow Chemical Co Method for coating interior oven surfaces to provide easy soil removal
US4003393A (en) * 1973-02-14 1977-01-18 The Dow Chemical Company Gel-like composition for use as a pig in a pipeline
US4038207A (en) * 1975-11-03 1977-07-26 Borg-Warner Corporation Stabilized hydrocarbon gels and a method for their preparation
US4174283A (en) * 1976-02-06 1979-11-13 The Dow Chemical Company Method of fracturing with gelled organic liquids
US4152289A (en) * 1976-02-06 1979-05-01 The Dow Chemical Company Gelling of organic liquids
US4153649A (en) * 1976-02-09 1979-05-08 The Dow Chemical Company Phosphate ester-type reaction product and method of preparing same
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