US2877181A - Stabilized calcium fatty acid base grease - Google Patents

Stabilized calcium fatty acid base grease Download PDF

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US2877181A
US2877181A US582091A US58209156A US2877181A US 2877181 A US2877181 A US 2877181A US 582091 A US582091 A US 582091A US 58209156 A US58209156 A US 58209156A US 2877181 A US2877181 A US 2877181A
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grease
fatty acid
estolide
calcium
mixture
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John P Dilworth
Uhrig Karl
Harry C Becker
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Texaco Inc
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    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/067Polyaryl amine alkanes
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    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention relates to novel anhydrous calcium fatty acid greases. More particularly, this invention discloses a novel additive that stabilizes anhydrous calcium fatty acid greases.
  • Anhydrous calcium fatty acid greases require the presence of a stabilizer such as glycerol monostearate or calcium acetate to prevent separation of the components.
  • This invention involves the discovery of a novel stabilizer for calcium fatty acid greases which has the additional advantage of increasing grease yields.
  • the anhydrous calcium base grease compositions of this invention comprise an oleaginous lubricating base as the major component, a calcium salt of a C to C fatty acid as the thickening agent and 0.5 to 3.0 Weight percent estolide of a C to C hydroxy fatty acid. It is necessary to shock cool the estolide-containing calcium fatty acid greases of this invention from a temperature of 190 to about 100 F. in order for the estolide to act as a stabilizer.
  • estolide of a hydroxy fatty acid as a stabilizer for calcium fatty acid greases has the additional advantage that the preferred estolide concentration elfects a substantial improvement in the yield of a calcium fatty acid base grease.
  • Estolide concentrations falling between 1 and 2.5 weight percent of the total grease composition substantially harden the grease mixtures so that it is possible to obtain the desired grease grade with less soap concentration.
  • the action of the estolides in calcium fatty acid base greases in this re spect is similar to their action on sodium fatty acid base greases as disclosed in the commonly assigned copending application Serial No. 533,232, filed September 8, 1955, by J. R. Roach, J. F. Lyons and J. P. Dilworth.
  • estolides which act as stabilizers for the anhydrous calcium fatty acid greases of this invention are intermolecular esters and polyesters of C to C hydroxy fatty acidshaving the following general formula HO imo-i50 wherein R is an alkyl group of 6' carbon atoms and n is an integer having a value of 2 to 12.
  • the estolides eral formula . areformed by heat treatment of 12-hydroxy stearic acid at temperatures between 200 and 300 F. and subsequent extractionof the estolides from the heat-treated hydroxy stearic acid with an aliphatic hydrocarbon solvent such as hexane.
  • the preferred estolides of 12-hydroxy stearic acid have an average molecular weight between 800 and 3000, indicating that the estolide fraction comprises mainly trimers, tetramers, pentamers and hexamers.
  • the minimum estolide concentration required for stabilization of the anhydrous calcium fatty acid greases is 0.5 weight percent of the total grease composition.
  • the upper concentration limit is' placed at 3 weight percent of the total grease composition because higher concentrations of estolide result in decrease of the grease yield.
  • the preferred estolide concentration for both stabilization and yield increase falls between 1.0 and 2.5 Weight percent of the grease composition.
  • Grease stabilization and hardening are effected Whether the estolide,.in the prescribed amount, is added during the grease manufacture or to the finished grease. Regardless of whether the estolide is added with the charge, after dehydration or to the grease mixture on reheating to 320 F., stabilization and hardening are obtained as long as the estolide-containing grease mixture is shock cooled from 190 to about F. When.
  • the estolide is added to a mixture of oil and calcium soap, which has separated because of the absence of stabilizer, stabilization is obtained by heating the estolidecontaining mixture to about 300 F. with stirring to effect uniform distribution of the estolide throughout the grease mixture, cooling to about200 F. without regard to the rate of cooling, and then shock cooling from about 190 to about 100 F.
  • the calcium salt of theestolide is present in the finished grease composition.
  • the estolides and the calcium salts are equivalent in function in producing a stable product and in improving the yield.
  • a surprising feature of this invention is thenecessity of shock cooling the grease from a temperature of about 190 to about 100 F. in order to produce a stable product.
  • Shock cooling denotes cooling at an average rate above 2 F. per minute.
  • Cooling of the grease mixture from 190 F. can; be effected in a number of ways. vOne procedure involves drawing the grease into shallow cooling pans. Another procedure involves passing the grease over a heat exchangesurface in a thin film. The use of a shallow cooling pan is the most convenient procedure for obtaining the shock cooling necessary in this invention.
  • the remaining procedure for preparing the grease products of this invention is conventional.
  • a recommended procedure involves mixing oleaginous lubricating base, fatty acid, lime and a small amount of water, saponifying the mixture at a temperature about to 200 F. and dehydrating the saponified mixture at a temperature in the range of 270 to 320 F.
  • the remainder of oleaginous lubricating base is added during stirred cooling of the grease to a temperature above F. at which time the grease is drawn and shock cooled as described above.
  • the thickening agents of the grease compositions of this invention are calcium soaps of fatty acids containing 12 to 24 carbon atoms.
  • the calcium soaps can be prepared from fats and fatty oils, the fatty acids per so are preferably employed.
  • Calcium salts of hydroxy fatty acids are specifically excluded from the thickening agents contemplated in this invention. Examples of fatty acids that are used in this invention are stearic acid, myristic acid, palmitic acid, arachidic acid, behenic acid, lauric acid, oleic acid and mixtures thereof.
  • the concentration of the calcium soap varies within wide limits depending upon the grade of grease desired. In general, the soap concentration falls within the range of 5 to'3O percent of the total grease composition with concentrations between 6 and 15 percent usually being employed.
  • the oleaginous lubricating base may be a conventional mineral lubricating oil, a synthetic lubricating oil prepared by cracking and polymerizing products of the Fischer-Tr'opsch process and the like or a synthetic oleaginous compound possessing lubricating characteristics and having an SUS viscosity within the lubricating oil viscosity range.
  • the oleaginous base is usually a conventional mineral lubricating oil because of the cost factor, but a synthetic base material can be substituted in all or in part therefor.
  • the mineral lubricating oils can be a distillate or residual oil and can be derived from a paraflin base, naphthene base or mixed paraffin-naphthene base crude. These mineral lubricating oils are subjected to greater or lesser degrees of refining and solvent dewaxing, depending upon the use intended for the grease composition.
  • the greases of-this invention can be formulated with mineral lubricating oils having an SUS viscosity at 100 F. between 50 and 1000, but are usually prepared with base oils having an SUS viscosity at 100 F. between 50 and 300.
  • the synthetic lubricating bases are usually of the ester or other type.
  • High boiling esters of aliphatic dicarboxylic acids find particularly wide-spread use in greases adapted for extreme temperature lubrication, that is, lubrication at both high and low temperatures.
  • Examples of the synthetic polyester lubricating bases are: di-Z-ethylhexyl sebacate, di-2-ethylhexyl azelate, di-n-amyl sebacate, di-Z-ethylhexyl adipate, and di-n-nonyl azelate.
  • Polyalkyleneethers such as polyethylene glycol, polypropylene glycol, modified by etherification and esterification of the terminal hydroxy radicals, are also useful synthetic lubricating bases.
  • Aromatic amine type inhibitors have been found particularly effective anti-oxidants; aromatic amines such as N,N,N',N'-tetramethyl 4,4'-diamino diphenyl methane, diphenyl amine and phenyl alphanaphthyl amine are preferred.
  • Extreme pressure additives which may be incorporated in the greases are sulfurized fats, sulfurized oils, chlorinated organic compounds such as chloro-substituted waxes, chloro-substituted aromatic compounds and chlorinated olefin polymers and sulfo-chlorinated compounds such as sulfo-chlorinated olefin polymers and olefins derived from waxes.
  • the concentration of oleaginous lubricating bases varies between 60 and 94 percent of the total grease composition and usually falls between 85 and 90 percent of the composition.
  • estolides stabilizes calcium fatty acid greases and improves the yields thereof when present in the preferred amount.
  • the necessity of shock cooling the grease from a temperature of 190 F. is also demonstrated in the following examples.
  • Example 1 Example 2 Using the same oil, an attempt was made to prepare a. stable calcium stearate grease employing as a stabilizer an estolide of 12-hydroxy stearic acid having an average molecular weight of about 2500. To this end 1430 grams .of stearic acid, 131 grams of estolide, 222 grams of lime and 2.5 lbs. of water were added to 3.5 lbs. of the aforeidentified paraflin base oil. After saponification at a tem- 4 perature of to 200 F. for 4 hours, the grease mixture was dehydrated at a temperature of 270 to 275 F. for 3 hours.
  • the mixture was allowed to cool statically from 190 F. to room temperature from midnight to 8:00 a. m. in the kettle.
  • the mixture separated into soap and oil on standing.
  • Example 3 This example was a duplicate of Example 2 with the exception that the estolide-containing grease mixture was shock cooled.
  • a reaction mixture was formed comprising 1430 grams of stearic acid, 131 grams of estolide, 222 grams of lime, 2.5 lbs. of water and 3.5 lbs. of paraflin base oil.
  • the reaction mixture was saponified at a temperature of 180 to 200 F. for 4 hours and then dehydrated at a temperature of 270 to 275 F. for 3 hours.
  • the remainder of the paraffin base oil, 19.3 lbs., and 64 grams of diphenylamine were added during the stirred cooling at a rate of 012 F. per minute to about 190 F.
  • the mixture was drawn into shallow cooling pans having a depth of A to /2 inch and shock cooled from 190 F. to room temperature.
  • the average cooling rate was more than 2 F. per minute.
  • the resulting grease was dark brown, stifi and glossy and became smooth and buttery-like on working.
  • the product was a No. 3 grade grease having a worked penetration of 232. Its
  • composition was as follows:
  • a stable anhydrous calcium grease comprising an oleaginous lubricating base as the major component, a calcium salt of a C to C unsubstituted fatty acid as the thickening agent and 0.5 to 3 weight percent of a compound selected from the group consisting of an estolide of a hydroxy fatty acid containing 12 to 24 cafbon atoms, a calcium salt of said estolide and a mixture thereof said estolide having an average molecular weight between 500 and 3500 said grease having been shock cooled from a-temperature of 190 F. to about 100 F.
  • estolide has the following general formula and the estolide is derived from 12-hydroxy stearic acid 5 and has an average molecular weight of between 800 and 3000.
  • a process for preparing a stable anhydrous calcium grease of a C to C unsubstituted fatty acid which comprises adding a compound selected from the group consisting of estolides, calcium salts thereof and mixtures thereof, said estolide being derived from a hydroxy fatty acid containing 12 to 24 carbon atoms and having an average molecular weight between 500 and 3500 to an anhydrous grease mixture, comprising an oleaginous lubricating base and the calcium soap of said C to C fatty acid as the thickening agent, heating the resulting grease mixture to a temperature of about 300 F., cooling said mixture to a temperature of about 190 6 F. and shock cooling said mixture from a temperature of 190 F. to about 100 F.
  • shock cooling is effected by drawing said grease at a temperature of 190 E. into shallow cooling pans.

Description

United States Paten 2,877,181 Patented Mar. 10, 1959 [ice STABILIZED CALCIUM FATTY ACID BASE GREASE John P. Dilworth, Fishkill, Karl Uhrig, Beacon, and Harry C. Becker, Fishkill, N. Y., assignors to The Texas Company, New York, N. Y., a corporation of Delaware No Drawing. Application May 2, 1956 Serial No. 582,091
7 Claims. (Cl. 252-405) This invention relates to novel anhydrous calcium fatty acid greases. More particularly, this invention discloses a novel additive that stabilizes anhydrous calcium fatty acid greases.
Anhydrous calcium fatty acid greases require the presence of a stabilizer such as glycerol monostearate or calcium acetate to prevent separation of the components. This invention involves the discovery of a novel stabilizer for calcium fatty acid greases which has the additional advantage of increasing grease yields.
The anhydrous calcium base grease compositions of this invention comprise an oleaginous lubricating base as the major component, a calcium salt of a C to C fatty acid as the thickening agent and 0.5 to 3.0 Weight percent estolide of a C to C hydroxy fatty acid. It is necessary to shock cool the estolide-containing calcium fatty acid greases of this invention from a temperature of 190 to about 100 F. in order for the estolide to act as a stabilizer.
The use of an estolide of a hydroxy fatty acid as a stabilizer for calcium fatty acid greases has the additional advantage that the preferred estolide concentration elfects a substantial improvement in the yield of a calcium fatty acid base grease. Estolide concentrations falling between 1 and 2.5 weight percent of the total grease composition substantially harden the grease mixtures so that it is possible to obtain the desired grease grade with less soap concentration. The action of the estolides in calcium fatty acid base greases in this re spect is similar to their action on sodium fatty acid base greases as disclosed in the commonly assigned copending application Serial No. 533,232, filed September 8, 1955, by J. R. Roach, J. F. Lyons and J. P. Dilworth.
The estolides which act as stabilizers for the anhydrous calcium fatty acid greases of this invention are intermolecular esters and polyesters of C to C hydroxy fatty acidshaving the following general formula HO imo-i50 wherein R is an alkyl group of 6' carbon atoms and n is an integer having a value of 2 to 12. The estolides eral formula .areformed by heat treatment of 12-hydroxy stearic acid at temperatures between 200 and 300 F. and subsequent extractionof the estolides from the heat-treated hydroxy stearic acid with an aliphatic hydrocarbon solvent such as hexane. The preferred estolides of 12-hydroxy stearic acid have an average molecular weight between 800 and 3000, indicating that the estolide fraction comprises mainly trimers, tetramers, pentamers and hexamers.
The minimum estolide concentration required for stabilization of the anhydrous calcium fatty acid greases is 0.5 weight percent of the total grease composition. The upper concentration limit is' placed at 3 weight percent of the total grease composition because higher concentrations of estolide result in decrease of the grease yield. The preferred estolide concentration for both stabilization and yield increase falls between 1.0 and 2.5 Weight percent of the grease composition.
Grease stabilization and hardening are effected Whether the estolide,.in the prescribed amount, is added during the grease manufacture or to the finished grease. Regardless of whether the estolide is added with the charge, after dehydration or to the grease mixture on reheating to 320 F., stabilization and hardening are obtained as long as the estolide-containing grease mixture is shock cooled from 190 to about F. When.
the estolide is added to a mixture of oil and calcium soap, which has separated because of the absence of stabilizer, stabilization is obtained by heating the estolidecontaining mixture to about 300 F. with stirring to effect uniform distribution of the estolide throughout the grease mixture, cooling to about200 F. without regard to the rate of cooling, and then shock cooling from about 190 to about 100 F.
If excess calcium hydroxide is present during the manufacture of the grease, the calcium salt of theestolide is present in the finished grease composition. The estolides and the calcium salts are equivalent in function in producing a stable product and in improving the yield.
A surprising feature of this invention is thenecessity of shock cooling the grease from a temperature of about 190 to about 100 F. in order to produce a stable product. Shock cooling denotes cooling at an average rate above 2 F. per minute.
Cooling of the grease mixture from 190 F. can; be effected in a number of ways. vOne procedure involves drawing the grease into shallow cooling pans. Another procedure involves passing the grease over a heat exchangesurface in a thin film. The use of a shallow cooling pan is the most convenient procedure for obtaining the shock cooling necessary in this invention.
The remaining procedure for preparing the grease products of this invention is conventional. A recommended procedure involves mixing oleaginous lubricating base, fatty acid, lime and a small amount of water, saponifying the mixture at a temperature about to 200 F. and dehydrating the saponified mixture at a temperature in the range of 270 to 320 F. The remainder of oleaginous lubricating base is added during stirred cooling of the grease to a temperature above F. at which time the grease is drawn and shock cooled as described above.
The thickening agents of the grease compositions of this invention are calcium soaps of fatty acids containing 12 to 24 carbon atoms. Although the calcium soaps can be prepared from fats and fatty oils, the fatty acids per so are preferably employed. Calcium salts of hydroxy fatty acids are specifically excluded from the thickening agents contemplated in this invention. Examples of fatty acids that are used in this invention are stearic acid, myristic acid, palmitic acid, arachidic acid, behenic acid, lauric acid, oleic acid and mixtures thereof.
The concentration of the calcium soap varies within wide limits depending upon the grade of grease desired. In general, the soap concentration falls within the range of 5 to'3O percent of the total grease composition with concentrations between 6 and 15 percent usually being employed.
The oleaginous lubricating base may be a conventional mineral lubricating oil, a synthetic lubricating oil prepared by cracking and polymerizing products of the Fischer-Tr'opsch process and the like or a synthetic oleaginous compound possessing lubricating characteristics and having an SUS viscosity within the lubricating oil viscosity range. The oleaginous base is usually a conventional mineral lubricating oil because of the cost factor, but a synthetic base material can be substituted in all or in part therefor.
The mineral lubricating oils can be a distillate or residual oil and can be derived from a paraflin base, naphthene base or mixed paraffin-naphthene base crude. These mineral lubricating oils are subjected to greater or lesser degrees of refining and solvent dewaxing, depending upon the use intended for the grease composition. Broadly speaking, the greases of-this invention can be formulated with mineral lubricating oils having an SUS viscosity at 100 F. between 50 and 1000, but are usually prepared with base oils having an SUS viscosity at 100 F. between 50 and 300.
The synthetic lubricating bases are usually of the ester or other type. High boiling esters of aliphatic dicarboxylic acids find particularly wide-spread use in greases adapted for extreme temperature lubrication, that is, lubrication at both high and low temperatures. Examples of the synthetic polyester lubricating bases are: di-Z-ethylhexyl sebacate, di-2-ethylhexyl azelate, di-n-amyl sebacate, di-Z-ethylhexyl adipate, and di-n-nonyl azelate. Polyalkyleneethers such as polyethylene glycol, polypropylene glycol, modified by etherification and esterification of the terminal hydroxy radicals, are also useful synthetic lubricating bases.
Additives to impart anti-oxidant and extreme pressure properties may be incorporated in the greases of the invention. Aromatic amine type inhibitors have been found particularly effective anti-oxidants; aromatic amines such as N,N,N',N'-tetramethyl 4,4'-diamino diphenyl methane, diphenyl amine and phenyl alphanaphthyl amine are preferred. Extreme pressure additives which may be incorporated in the greases are sulfurized fats, sulfurized oils, chlorinated organic compounds such as chloro-substituted waxes, chloro-substituted aromatic compounds and chlorinated olefin polymers and sulfo-chlorinated compounds such as sulfo-chlorinated olefin polymers and olefins derived from waxes.
The concentration of oleaginous lubricating bases varies between 60 and 94 percent of the total grease composition and usually falls between 85 and 90 percent of the composition.
The following examples demonstrate that the presence of estolides stabilizes calcium fatty acid greases and improves the yields thereof when present in the preferred amount. The necessity of shock cooling the grease from a temperature of 190 F. is also demonstrated in the following examples.
Example 1 Example 2 Using the same oil, an attempt was made to prepare a. stable calcium stearate grease employing as a stabilizer an estolide of 12-hydroxy stearic acid having an average molecular weight of about 2500. To this end 1430 grams .of stearic acid, 131 grams of estolide, 222 grams of lime and 2.5 lbs. of water were added to 3.5 lbs. of the aforeidentified paraflin base oil. After saponification at a tem- 4 perature of to 200 F. for 4 hours, the grease mixture was dehydrated at a temperature of 270 to 275 F. for 3 hours. The remainder of the parafiin base oil, namely 19.3 lbs., and 64 grams of diphenylamine were added as the mixture was slowly cooled at about 0.12" F. per minute to about F. The mixture was allowed to cool statically from 190 F. to room temperature from midnight to 8:00 a. m. in the kettle. The mixture separated into soap and oil on standing.
Example 3 This example was a duplicate of Example 2 with the exception that the estolide-containing grease mixture was shock cooled. A reaction mixture was formed comprising 1430 grams of stearic acid, 131 grams of estolide, 222 grams of lime, 2.5 lbs. of water and 3.5 lbs. of paraflin base oil. The reaction mixture was saponified at a temperature of 180 to 200 F. for 4 hours and then dehydrated at a temperature of 270 to 275 F. for 3 hours. The remainder of the paraffin base oil, 19.3 lbs., and 64 grams of diphenylamine were added during the stirred cooling at a rate of 012 F. per minute to about 190 F. The mixture was drawn into shallow cooling pans having a depth of A to /2 inch and shock cooled from 190 F. to room temperature. The average cooling rate was more than 2 F. per minute. The resulting grease was dark brown, stifi and glossy and became smooth and buttery-like on working. The product was a No. 3 grade grease having a worked penetration of 232. Its
composition was as follows:
Percent by wt. Calcium stear 12.4 Calcium soap of estolide 1.3 Excess calcium hydroxide 0.2 Base oil 85.6 Diphenylamine 0.5
grease from a temperature about 190 F. to room temperature in order for the estolide to be an effective stabilizer.
Obviously, many modifications and variations of the invention, as hereinbefore set forth, may be made without departing from the spirit and scope thereof, and, therefore, only such limitations should be imposed as are indicated in the appended claims.
We claim:
1. A stable anhydrous calcium grease comprising an oleaginous lubricating base as the major component, a calcium salt of a C to C unsubstituted fatty acid as the thickening agent and 0.5 to 3 weight percent of a compound selected from the group consisting of an estolide of a hydroxy fatty acid containing 12 to 24 cafbon atoms, a calcium salt of said estolide and a mixture thereof said estolide having an average molecular weight between 500 and 3500 said grease having been shock cooled from a-temperature of 190 F. to about 100 F.
2. An anhydrous calcium base grease according to claim 1 in which said estolide has the following general formula and the estolide is derived from 12-hydroxy stearic acid 5 and has an average molecular weight of between 800 and 3000.
5. A process for preparing a stable anhydrous calcium grease of a C to C unsubstituted fatty acid which comprises adding a compound selected from the group consisting of estolides, calcium salts thereof and mixtures thereof, said estolide being derived from a hydroxy fatty acid containing 12 to 24 carbon atoms and having an average molecular weight between 500 and 3500 to an anhydrous grease mixture, comprising an oleaginous lubricating base and the calcium soap of said C to C fatty acid as the thickening agent, heating the resulting grease mixture to a temperature of about 300 F., cooling said mixture to a temperature of about 190 6 F. and shock cooling said mixture from a temperature of 190 F. to about 100 F.
6. A process according to claim 5 in which said shock cooling is effected by drawing said grease at a temperature of 190 E. into shallow cooling pans.
7. A process according to claim 5 in which the mixture is cooled from 190 F. to about 100 F. at an average rate above 2 F. per minute.
References Cited in the file of this patent UNITED STATES PATENTS 2,475,589 Bondi July 12, 1949 2,607,734 Sproule et al. Aug. 19, 1952 2,695,878 Entwistle Nov. 30, 1954

Claims (1)

1. A STABLE ANHYDROUS CALCIUM GREASE COMPRISING AN OLEAGINOUS LUBRICATING BASE AS THE MAJOR COMPONENT, A CALCIUM SALT OF A C12 TO C24 UNSUBSTITUATED FATTY ACID AS THE THICKENING AGENT AND 0.5 TO 3 WEIGHT PERCENT OF A COMPOUND SELECTED FROM THE GROUP CONSISTING OF AN ESTOLIDE OF A HYDROXY FATTY ACID CONTAINING 12 TO 24 CARBON ATOMS, A CALCIUM SALT OF SAID ESTOLIDE AND A MIXTURE THEREOF SAID ESTOLIDE HAVING AN AVERAGE MOLECULAR WEIGHT BETWEEN 500 AND 3500 SAID GREASE HAVING BEEN SHOCK COOLED FROM A TEMPERATURE OF 190* F. TO ABOUT 100* F.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3068173A (en) * 1959-08-24 1962-12-11 Texaco Inc Process for preparing complex calcium salt-calcium soap grease
US3068174A (en) * 1959-08-24 1962-12-11 Texaco Inc Process for preparing complex calcium salt-calcium soap grease
US4715973A (en) * 1985-03-15 1987-12-29 Shell Oil Company Lubricating oil compositions
US5427704A (en) * 1994-01-28 1995-06-27 The Lubrizol Corporation Triglyceride oils thickened with estolides of hydroxy-containing triglycerides
US5451332A (en) * 1994-01-28 1995-09-19 The Lubrizol Corporation Estolides of hydroxy-containing triglycerides that contain a performance additive
US5458795A (en) * 1994-01-28 1995-10-17 The Lubrizol Corporation Oils thickened with estolides of hydroxy-containing triglycerides
WO2012177549A1 (en) * 2011-06-21 2012-12-27 The Lubrizol Corporation Lubricating composition containing a dispersant
CN103555397A (en) * 2013-10-23 2014-02-05 中国石油化工股份有限公司 Anhydrous calcium-based lubricating grease composition and preparation method thereof
US20180044605A1 (en) * 2015-02-11 2018-02-15 Shell Oil Company Grease composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475589A (en) * 1947-04-18 1949-07-12 Shell Dev Lubricating grease composition
US2607734A (en) * 1950-05-20 1952-08-19 Standard Oil Dev Co Process of manufacturing hydroxy acid greases and product thereof
US2695878A (en) * 1951-02-17 1954-11-30 Sinclair Refining Co Greases containing a lithium soap of polymerized 12-hydroxy stearic acid and their method of manufacture

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475589A (en) * 1947-04-18 1949-07-12 Shell Dev Lubricating grease composition
US2607734A (en) * 1950-05-20 1952-08-19 Standard Oil Dev Co Process of manufacturing hydroxy acid greases and product thereof
US2695878A (en) * 1951-02-17 1954-11-30 Sinclair Refining Co Greases containing a lithium soap of polymerized 12-hydroxy stearic acid and their method of manufacture

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3068173A (en) * 1959-08-24 1962-12-11 Texaco Inc Process for preparing complex calcium salt-calcium soap grease
US3068174A (en) * 1959-08-24 1962-12-11 Texaco Inc Process for preparing complex calcium salt-calcium soap grease
US4715973A (en) * 1985-03-15 1987-12-29 Shell Oil Company Lubricating oil compositions
US5427704A (en) * 1994-01-28 1995-06-27 The Lubrizol Corporation Triglyceride oils thickened with estolides of hydroxy-containing triglycerides
US5451332A (en) * 1994-01-28 1995-09-19 The Lubrizol Corporation Estolides of hydroxy-containing triglycerides that contain a performance additive
US5458795A (en) * 1994-01-28 1995-10-17 The Lubrizol Corporation Oils thickened with estolides of hydroxy-containing triglycerides
WO2012177549A1 (en) * 2011-06-21 2012-12-27 The Lubrizol Corporation Lubricating composition containing a dispersant
US9249699B2 (en) 2011-06-21 2016-02-02 The Lubrizol Corporation Lubricating composition containing a dispersant
CN103555397A (en) * 2013-10-23 2014-02-05 中国石油化工股份有限公司 Anhydrous calcium-based lubricating grease composition and preparation method thereof
US20180044605A1 (en) * 2015-02-11 2018-02-15 Shell Oil Company Grease composition

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