US2953528A - Lubricating grease thickened with lithium soap of styrenated fatty acid - Google Patents

Lubricating grease thickened with lithium soap of styrenated fatty acid Download PDF

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US2953528A
US2953528A US666222A US66622257A US2953528A US 2953528 A US2953528 A US 2953528A US 666222 A US666222 A US 666222A US 66622257 A US66622257 A US 66622257A US 2953528 A US2953528 A US 2953528A
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grease
fatty acid
styrenated
lithium
grams
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John B O'neil
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Texaco Inc
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Texaco Inc
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125—Carboxylix 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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/082—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type monocarboxylic
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/086—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/102—Polyesters
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064—Di- and triaryl amines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064—Di- and triaryl amines
    • C10M2215/065—Phenyl-Naphthyl amines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/067—Polyaryl amine alkanes
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/02—Unspecified siloxanes; Silicones
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04—Siloxanes with specific structure
    • C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/02—Groups 1 or 11
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/02—Bearings
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10—Semi-solids; greasy

Definitions

  • This invention relates to improved lubricating greases, and more particularly to lubricating greases thickened with lithium soaps of styrenated fatty acids.
  • styrenated fatty acid materials may be employed very successfully 'in the preparation of lithium base lubricating greases, either as the sole saponifiable material or in admixture with other saponifiable materials of conventionaltypes.
  • Lubricatinggreases are obtained in this manner having very superior shear resistance and other special properties as compared with lithium base greases prepared from conventionalfatty acid materials, and in addition the use of such saponifiable materials permits the grease preparationto be carried out by the convenient low temperature method, wherein the saponification and: dehydration are carried out at temperatures belowthe melting point of the soap.
  • the styrenated fatty acid materials which are employed as the' saponifiablematerials forproducing the greases of this invention are additionproducts of unsaturated highmolecularweight fattyacidsand their esters with styrene; They are readily obtained by heating together the unsaturated fatty acid material and styrene, as described'for example, by P. Powers, Industrial and Engineering-Chemistry, volume 42, page2097-99 (1950). Thereaction apparently proceeds wtih saturation of the styrene double bond, producing unsaturated i United States Patent 0 fatty acids having a phenyl ethyl groupattached to one of the carbonatoms linkedbythe double bonds.
  • the reaction product may containvarious polymeric compounds containing more than one styreneparticle for each fatty acid molecule'and also compounds containing'two or more carboxylic acid groups, obtained by cross-linking reactions.
  • Suitable starting materials forthestyrenationireaction are unsaturated fatty acids containing atleast 12. carbon atoms, such as from 12 to about 32 carbon. atomsper molecule, and one or more olefinic double bonds per molecule, and the glycerides or other esters of such acids. form or in naturally occurring mixtures with each other and with minor proportions of saturated fatty'acids' and their esters derived from animal, vegetable or marine oils, such as, for example, lard. oil, cottonseed oil, linseed oil,-castor oil, menhaden oil, whale oil,' etc.
  • the preferred starting materials are .those' consisting of at least a predorninantiproportion ofunsaturated fatty'a'cids containing: from about 16' to about 24 carbon atoms They may be. employed either in relatively pure andeither l or 2 olefinic double 'bondspermolecule, such ice ylenic acid, erucic acid and ricinoleic acid, and the esters-of such acids.
  • The'lubricating greases of this invention suitably contain from about 5 to about 50 percent by Weight of the lithium soap of a styrenated fatty acid material as described above, either alone or in conjunctionwith other thickening agents such as different fatty acid soaps.
  • the thickening agent may comprise a lithium soap of styrenated fatty acid material together with a lithium soap of a different fatty acid material, such as unsubstituted fatty acids and hydroxy fatty acids of the types which have been employed heretofore in grease making, in a ratio of from about 1 to 3 to about nowadays to 1- by-weight, and preferably in a ratio of from about-1 to 2 to about 2 to 1 by Weight.
  • the oleaginous liquids employed in these greases may be any oils suitablefor use in grease making generally, such as mineral oils obtained by any of the conventional refining processes in the lubricating oil viscosity range, preferably those'having'viscosities from about seconds Saybolt Universal at F; to about 225 seconds at 210 F.
  • various synthetic oils may be employed with advantage, such as high molecular weight ethers; esters, and silicone polymer oils.
  • Particularly suitable synthetic esters are dicarboxylic acid esters, such as, for example, di-Z-ethylhexyl sebacate, di (s'econdary amyl) sebacate, and di-2-ethylhexyl azelate.
  • the greases may also contain various additives of the usual types employed in lubricating greases, such as corrosion inhibitors, oxidation inhibitors, antiwear agents, etc.
  • they contain an oxidation inhibitor, which may suitably be an oxidation inhibitor of the amine type; such as diphenylamine, phenyl naphthylamine or tetramethyl diamino diphenyl methane.
  • the grease preparation may be carried out by any suitable grease making procedure: It is preferably carried out byvthemethod involving saponification in situ,
  • the saponification of the styrenated fatty acid material, or a mixture of such material with other saponifiablesfatty' acid material as described above is carried out in a portion of the lubricating oil employed as the liquid base.
  • the oil employed in the saponification is preferably a mineral oil or other oil which is not hydrolyzed under the saponification conditions.
  • the saponification mass is heated at a higher temperature to dehydrate, and the main portion of" theoleaginous liquid component and any additives employed are mixed in While the grease is allowed to cool.
  • the styrenated fatty acid material may be prepared by heating together the unsaturated fatty acid material and styrene at temperatures in about the range to 300 -C., employing the fatty acid material and styrene in a ratio from about 1 to 2 to 2 to 1 by weight. It is preferably carried out at temperatures in about a range ISO-260 C. employing the fatty acid material and styrene in about equal amounts by weight.
  • Example I A grease was prepared having the following composition in percent by weight:
  • Lithium soap of styrenated oleic acid 16.5 Phenyl alpha naphthylamine 0.4
  • Mineral lubricating oil Remainder The mineral lubricating oil was a refined naphthene base distillate oil having a Saybolt Universal viscosity of 312 seconds at 100 F. g
  • the styrenated oleic acid was prepared by heating together 1000 grams of oleic acid, having a neutralization number of 195, a saponification number of 197 and an iodine number of 84, and 1000 grams of styrene at 150 C. under reflux for hours and then for anadditional 16 hours at 150-260 C. The product was then cooled quickly by drawing in thin layers. A hard brittle solid was obtained having a neutralization number of 84, an iodine number of 41 and a melting point (Fisher Block) of 158176 F.
  • the grease preparation was carried out in the following manner: A laboratory grease kettle was charged with 290 grams of the styrenated oleic acid, 300 grams of the mineral lubricating oil and 138 grams of 10 percent aqueous solution of lithium hydroxide. This mixture was heated for 1 hour at 200 F. until the saponification was complete and then at 300 F. for an additional hour to dehydrate. An additional 300 grams of the mineral lubricating oil was added While the temperature of the mass was maintained at 300 F., and 904 grams more of the oil was added gradually While the mixture was cooling from 300 F. to 220 F. The inhibitor was then added, and the grease finally drawn at 210 F. and finished by milling with two passes through a Premier Colloid Mill at 0.002 inch clearance.
  • the Grease Breakdown Machine Test is a test for determining the ability of a grease to lubricate ball bearings at high rotative speeds and elevated temperatures. It is carried out as described in US. 2,600,058, column 6, lines 11-70, by rotating a ball bearing lubricated with the grease under test at 3450 r.p.m. at increasing temperatures up to 300 F. The grease rating depends upon the amount of change which the grease has undergone in the test.
  • Example 11 A grease was prepared having the following composition in percent by weight:
  • the mineral lubricating oil was a refined paraffinic distillate oil having a viscosity of about 105 seconds Saybolt Universal at 100 F.
  • the synthetic ester was a commercial di-2-ethylhexyl sebacate, having a Flash Point, COC, of 410 F., a kinematic viscosity of 100 F. of 1.83 centistokes, and a Four Point below -65 F.
  • the styrenated oleic acid was the same as that described in Example I.
  • the grease preparation was carried out substantially as described in Example I, employing a kettle charge consisting of 580 grams of styrenated oleic acid, 400 grams of mineral oil and 515 grams of 10 percent aqueous solution of lithium hydroxide.
  • the synthetic ester was added following the dehydration and during the cooling. The milling step was omitted.
  • the grease obtained had a dropping point of 400 F. and an ASTM worked penetration of 342. It gave a pressure drop of 3 pounds in the Norma-Hoffman oxidation test at 210 F.
  • Example III A grease was prepared having the following composition in percent by weight:
  • Lithium soap of styrenated oleic acid 9.7 Lithium stearate 9.7 Phenyl alpha naphthylamine 0.5
  • Mineral lubricating oil Remainder The mineral lubricating oil was the same as that described in Example I.
  • the styrenated oleic acid was prepared by heating together 1,000 grams of oleic acid, having a neutralization and saponification number of 201 and an iodine number of 98, and 1,000 grams of styrene at about 150 C. under reflux for 5 hours, and then shock cooling the reaction product.
  • a hard brittle solid was obtained having a neutralization number of about 20 and a saponification number of about 105.
  • the grease preparation was carried out employing a kettle charge consisting of 198 grams of the styrenated oleic acid, 196 grams of stearic acid, 260 grams of 10 percent aqueous lithium hydroxide solution, 400 grams of mineral oil and 400 grams of water.
  • the saponification was carried out by heating the mixture for 2 hours at 210 F. and the dehydration was accomplished by heating for an additional hour at 310 F. After the dehydration, 400 grams more of the mineral oil were added while the temperature was maintained at 310 F., and an additional 850 grams were added during the cooling to 210 F. The inhibitor was then added and the grease was finally drawn at 204 F.
  • the uniform fibrous grease was obtained by the above procedure which gave the following tests.
  • Miniature penetration- The dynamic shear test is a test for measuring the resistance of a grease to texture change when worked under high shearing stress.
  • the test apparatus comprises a perforated piston reciprocating within a closed cylinder maintained at a constant temperature. The test was carried out by charging a sample of the grease to the cylinder maintained at 225 F. and reciprocating the piston at 49 strokes per minute for 8 hours. Miniature penetrations were taken upon the grease both before and after the test.
  • the miniature penetration test is described in Industrial and Engineering Chemistry, Analytical Edition, volume II, page 108 (February 15, 1939). As shown by the data, the grease of this invention gave only a small change in miniature penetration in this test, indicative of excellent shear stability. Greases thickened with lithium stearate break down in this test and become liquid or semi-liquid products.
  • the greases of the above examples which are representative of the greases of this invention, had high dropping points of above 350" F., good oxidation resistance and resistance to water washing and absorption, and excellent working stability. In addition, they gave very good bearing lubrication in engine testsunder actual service conditions.
  • a lubricating grease composition consisting essential-ly of a lubricating oil thickened to a grease consistency by a lithium fatty acid soap comprising at least 25 percent by weight of the lithium soap of a styrenated high molec/ ular weight unsaturated fatty acid.
  • composition according to claim 1 wherein the said styrenated unsaturated fatty acid is stytenated oleic acid.
  • composition according to claim 1 wherein the said lubricating oil is a mineral lubricating oil.
  • a lubricating grease composition consisting essentially of a lubricating oil thickened to a grease consistency by a mixture in about 1:3 to 3:1 ratio by weight of lithium soap of a styrenated high molecular weight unsaturated fatty acid and lithium soap of an unsubstituted high molecular weight fatty acid.
  • a lubricating grease consisting essentially of a mineral lubricating oil thickened to a grease consistency by about 5 to 50 percent by weight of a mixture in about a 1:2 to 2:1 ratio by weight of lithium soap of styrenated oleic acid and lithium stearate.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

LUBRICATING GREASE THICKENED WITH LITH- IUM SOAP OF STY-RENATED FATTY ACID John B. ONeil, Duxbury, Mass., assignor to Texaco Inc., a corporation of Delaware No Drawing. FiledJune 17, 1957, Ser. No. 666,222.
6 Claims. (Cl. 25242) This invention relates to improved lubricating greases, and more particularly to lubricating greases thickened with lithium soaps of styrenated fatty acids.
I have found that styrenated fatty acid materials may be employed very successfully 'in the preparation of lithium base lubricating greases, either as the sole saponifiable material or in admixture with other saponifiable materials of conventionaltypes. Lubricatinggreases are obtained in this manner having very superior shear resistance and other special properties as compared with lithium base greases prepared from conventionalfatty acid materials, and in addition the use of such saponifiable materials permits the grease preparationto be carried out by the convenient low temperature method, wherein the saponification and: dehydration are carried out at temperatures belowthe melting point of the soap.
The styrenated fatty acid materials which are employed as the' saponifiablematerials forproducing the greases of this invention are additionproducts of unsaturated highmolecularweight fattyacidsand their esters with styrene; They are readily obtained by heating together the unsaturated fatty acid material and styrene, as described'for example, by P. Powers, Industrial and Engineering-Chemistry, volume 42, page2097-99 (1950). Thereaction apparently proceeds wtih saturation of the styrene double bond, producing unsaturated i United States Patent 0 fatty acids having a phenyl ethyl groupattached to one of the carbonatoms linkedbythe double bonds. Styrenated oleic acid is considered'to be represented by the formula In addition to the sample monomeric addition" products represented by this formula, the reaction product may containvarious polymeric compounds containing more than one styreneparticle for each fatty acid molecule'and also compounds containing'two or more carboxylic acid groups, obtained by cross-linking reactions.
Suitable starting materials forthestyrenationireaction are unsaturated fatty acids containing atleast 12. carbon atoms, such as from 12 to about 32 carbon. atomsper molecule, and one or more olefinic double bonds per molecule, and the glycerides or other esters of such acids. form or in naturally occurring mixtures with each other and with minor proportions of saturated fatty'acids' and their esters derived from animal, vegetable or marine oils, such as, for example, lard. oil, cottonseed oil, linseed oil,-castor oil, menhaden oil, whale oil,' etc. The preferred starting materials are .those' consisting of at least a predorninantiproportion ofunsaturated fatty'a'cids containing: from about 16' to about 24 carbon atoms They may be. employed either in relatively pure andeither l or 2 olefinic double 'bondspermolecule, such ice ylenic acid, erucic acid and ricinoleic acid, and the esters-of such acids.
The'lubricating greases of this invention suitably contain from about 5 to about 50 percent by Weight of the lithium soap of a styrenated fatty acid material as described above, either alone or in conjunctionwith other thickening agents such as different fatty acid soaps. With particular advantage, the thickening agent may comprise a lithium soap of styrenated fatty acid material together with a lithium soap of a different fatty acid material, such as unsubstituted fatty acids and hydroxy fatty acids of the types which have been employed heretofore in grease making, in a ratio of from about 1 to 3 to about?! to 1- by-weight, and preferably in a ratio of from about-1 to 2 to about 2 to 1 by Weight.
The oleaginous liquids employed in these greases may be any oils suitablefor use in grease making generally, such as mineral oils obtained by any of the conventional refining processes in the lubricating oil viscosity range, preferably those'having'viscosities from about seconds Saybolt Universal at F; to about 225 seconds at 210 F. For certain purposes, such as for producing greases suitable for high'temperatureoperations, various synthetic oils may be employed with advantage, such as high molecular weight ethers; esters, and silicone polymer oils. Particularly suitable synthetic esters are dicarboxylic acid esters, such as, for example, di-Z-ethylhexyl sebacate, di (s'econdary amyl) sebacate, and di-2-ethylhexyl azelate.
The greases may also contain various additives of the usual types employed in lubricating greases, such as corrosion inhibitors, oxidation inhibitors, antiwear agents, etc. Preferably, they contain an oxidation inhibitor, which may suitably be an oxidation inhibitor of the amine type; such as diphenylamine, phenyl naphthylamine or tetramethyl diamino diphenyl methane.
The grease preparation may be carried out by any suitable grease making procedure: It is preferably carried out byvthemethod involving saponification in situ,
wherein the saponification of the styrenated fatty acid material, or a mixture of such material with other saponifiablesfatty' acid material as described above, is carried out in a portion of the lubricating oil employed as the liquid base. The oil employed in the saponification is preferably a mineral oil or other oil which is not hydrolyzed under the saponification conditions. Following the saponification, the saponification mass is heated at a higher temperature to dehydrate, and the main portion of" theoleaginous liquid component and any additives employed are mixed in While the grease is allowed to cool.
The styrenated fatty acid material may be prepared by heating together the unsaturated fatty acid material and styrene at temperatures in about the range to 300 -C., employing the fatty acid material and styrene in a ratio from about 1 to 2 to 2 to 1 by weight. It is preferably carried out at temperatures in about a range ISO-260 C. employing the fatty acid material and styrene in about equal amounts by weight.
The following examples are illustrative of the lubricating greases of this invention.
Example I A grease was prepared having the following composition in percent by weight:
Lithium soap of styrenated oleic acid 16.5 Phenyl alpha naphthylamine 0.4 Mineral lubricating oil Remainder The mineral lubricating oil was a refined naphthene base distillate oil having a Saybolt Universal viscosity of 312 seconds at 100 F. g
The styrenated oleic acid was prepared by heating together 1000 grams of oleic acid, having a neutralization number of 195, a saponification number of 197 and an iodine number of 84, and 1000 grams of styrene at 150 C. under reflux for hours and then for anadditional 16 hours at 150-260 C. The product was then cooled quickly by drawing in thin layers. A hard brittle solid was obtained having a neutralization number of 84, an iodine number of 41 and a melting point (Fisher Block) of 158176 F.
The grease preparation was carried out in the following manner: A laboratory grease kettle was charged with 290 grams of the styrenated oleic acid, 300 grams of the mineral lubricating oil and 138 grams of 10 percent aqueous solution of lithium hydroxide. This mixture was heated for 1 hour at 200 F. until the saponification was complete and then at 300 F. for an additional hour to dehydrate. An additional 300 grams of the mineral lubricating oil was added While the temperature of the mass was maintained at 300 F., and 904 grams more of the oil was added gradually While the mixture was cooling from 300 F. to 220 F. The inhibitor was then added, and the grease finally drawn at 210 F. and finished by milling with two passes through a Premier Colloid Mill at 0.002 inch clearance.
The product obtained as described above was a tan slightly stringy grease which gave the following tests:
The Grease Breakdown Machine Test is a test for determining the ability of a grease to lubricate ball bearings at high rotative speeds and elevated temperatures. It is carried out as described in US. 2,600,058, column 6, lines 11-70, by rotating a ball bearing lubricated with the grease under test at 3450 r.p.m. at increasing temperatures up to 300 F. The grease rating depends upon the amount of change which the grease has undergone in the test.
Example 11 A grease was prepared having the following composition in percent by weight:
Lithium soap of styrenated oleic acid 8.7 Phenyl alpha naphthylamine 0.2 Mineral lubricating oil 5.6 Synthetic ester Remainder The mineral lubricating oil was a refined paraffinic distillate oil having a viscosity of about 105 seconds Saybolt Universal at 100 F. The synthetic ester was a commercial di-2-ethylhexyl sebacate, having a Flash Point, COC, of 410 F., a kinematic viscosity of 100 F. of 1.83 centistokes, and a Four Point below -65 F.
The styrenated oleic acid was the same as that described in Example I.
The grease preparation was carried out substantially as described in Example I, employing a kettle charge consisting of 580 grams of styrenated oleic acid, 400 grams of mineral oil and 515 grams of 10 percent aqueous solution of lithium hydroxide. The synthetic ester was added following the dehydration and during the cooling. The milling step was omitted.
The grease obtained had a dropping point of 400 F. and an ASTM worked penetration of 342. It gave a pressure drop of 3 pounds in the Norma-Hoffman oxidation test at 210 F.
Example III A grease was prepared having the following composition in percent by weight:
Lithium soap of styrenated oleic acid 9.7 Lithium stearate 9.7 Phenyl alpha naphthylamine 0.5 Mineral lubricating oil Remainder The mineral lubricating oil was the same as that described in Example I.
The styrenated oleic acid was prepared by heating together 1,000 grams of oleic acid, having a neutralization and saponification number of 201 and an iodine number of 98, and 1,000 grams of styrene at about 150 C. under reflux for 5 hours, and then shock cooling the reaction product. A hard brittle solid was obtained having a neutralization number of about 20 and a saponification number of about 105.
The grease preparation was carried out employing a kettle charge consisting of 198 grams of the styrenated oleic acid, 196 grams of stearic acid, 260 grams of 10 percent aqueous lithium hydroxide solution, 400 grams of mineral oil and 400 grams of water. The saponification was carried out by heating the mixture for 2 hours at 210 F. and the dehydration was accomplished by heating for an additional hour at 310 F. After the dehydration, 400 grams more of the mineral oil were added while the temperature was maintained at 310 F., and an additional 850 grams were added during the cooling to 210 F. The inhibitor was then added and the grease was finally drawn at 204 F.
The uniform fibrous grease was obtained by the above procedure which gave the following tests.
Dropping point F 371 Penetration, ASTM, 77 F.:
Unworked 247 Worked 60 strokes 275 Worked 100,000 strokes 328 Norma-Hellman oxidation hrs. at 210 F., pressure drop, lbs Dynamic water resistance test, loss, percent 0 Dynamic shear test:
Miniature penetration- The dynamic shear test is a test for measuring the resistance of a grease to texture change when worked under high shearing stress. The test apparatus comprises a perforated piston reciprocating within a closed cylinder maintained at a constant temperature. The test was carried out by charging a sample of the grease to the cylinder maintained at 225 F. and reciprocating the piston at 49 strokes per minute for 8 hours. Miniature penetrations were taken upon the grease both before and after the test. The miniature penetration test is described in Industrial and Engineering Chemistry, Analytical Edition, volume II, page 108 (February 15, 1939). As shown by the data, the grease of this invention gave only a small change in miniature penetration in this test, indicative of excellent shear stability. Greases thickened with lithium stearate break down in this test and become liquid or semi-liquid products.
As shown by the data, the greases of the above examples which are representative of the greases of this invention, had high dropping points of above 350" F., good oxidation resistance and resistance to water washing and absorption, and excellent working stability. In addition, they gave very good bearing lubrication in engine testsunder actual service conditions.
assasas Obviously many modifications and variations of the invention, as hereinbefcre 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.
I claim:
1. A lubricating grease composition consisting essential-ly of a lubricating oil thickened to a grease consistency by a lithium fatty acid soap comprising at least 25 percent by weight of the lithium soap of a styrenated high molec/ ular weight unsaturated fatty acid.
2. A composition according to claim 1 wherein the said styrenated unsaturated fatty acid is stytenated oleic acid.
3. A composition according to claim 1 wherein the said lubricating oil is a mineral lubricating oil.
4. A composition according :to claim 1 wherein the said lubricating oil is a high molecular weight dicarboxylic acid di-ester.
5. A lubricating grease composition consisting essentially of a lubricating oil thickened to a grease consistency by a mixture in about 1:3 to 3:1 ratio by weight of lithium soap of a styrenated high molecular weight unsaturated fatty acid and lithium soap of an unsubstituted high molecular weight fatty acid.
6. A lubricating grease consisting essentially of a mineral lubricating oil thickened to a grease consistency by about 5 to 50 percent by weight of a mixture in about a 1:2 to 2:1 ratio by weight of lithium soap of styrenated oleic acid and lithium stearate.
References Cited in the file of this patent UNITED STATES PATENTS 2,586,693 Morway et a1. ..Feb. 19, 1952 2,692,232 Bartlett et a1. Oct. 19, 1954 2,868,814 Medalia et a1 Jan. 13, 1959 2,874,151 Medalia et a1 Feb. 17, 1959 OTHER REFERENCES Ind. & Eng. Chem., vol. 42, pp. 2097-2099 (1950).

Claims (2)

1. A LUBRICATING GREASE COMPOSITION CONSISTING ESSENTIALLY OF A LUBRICATING OIL THICKENED TO A GREASE CONSISTENCY BY A LITHIUM FATTY ACID SOAP COMPRISING AT LEAST 25 PERCENT BY WEIGHT OF THE LITHIUM SOAP OF A STYRENATED HIGH MOLECULAR WEIGHT UNSATURATED FATTY ACID.
4. A COMPOSITION ACCORDING TO CLAIM 1 WHEREIN THE SAID LUBRICATING OIL IS A HIGH MOLECULAR WEIGHT DICARBOXYLIC ACID DI-ESTER.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4879054A (en) * 1988-02-29 1989-11-07 Amoco Corporation Process for producing low temperature high performance grease

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2586693A (en) * 1949-11-01 1952-02-19 Standard Oil Dev Co Lubricating grease
US2692232A (en) * 1951-12-11 1954-10-19 Standard Oil Dev Co Lubricating grease compositions from hydroxy phenyl fatty acids
US2868814A (en) * 1953-11-02 1959-01-13 Gen Latex & Chemical Corp Composition of matter
US2874151A (en) * 1955-06-28 1959-02-17 Avrom I Medalia Polymeric emulsifying agents and their derivatives

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2586693A (en) * 1949-11-01 1952-02-19 Standard Oil Dev Co Lubricating grease
US2692232A (en) * 1951-12-11 1954-10-19 Standard Oil Dev Co Lubricating grease compositions from hydroxy phenyl fatty acids
US2868814A (en) * 1953-11-02 1959-01-13 Gen Latex & Chemical Corp Composition of matter
US2874151A (en) * 1955-06-28 1959-02-17 Avrom I Medalia Polymeric emulsifying agents and their derivatives

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4879054A (en) * 1988-02-29 1989-11-07 Amoco Corporation Process for producing low temperature high performance grease

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