US2586693A - Lubricating grease - Google Patents

Lubricating grease Download PDF

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US2586693A
US2586693A US124941A US12494149A US2586693A US 2586693 A US2586693 A US 2586693A US 124941 A US124941 A US 124941A US 12494149 A US12494149 A US 12494149A US 2586693 A US2586693 A US 2586693A
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acid
grease
soap
molecular weight
carbon atoms
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Arnold J Morway
Louis A Mikeska
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Standard Oil Development Co
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Standard Oil Development 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
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • 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
    • 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
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • 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
    • 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
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
    • 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
    • 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
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • 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
    • 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
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/124Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms containing hydroxy groups; Ethers thereof
    • 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
    • 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
    • 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
    • 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
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • 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
    • 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
    • C10M2215/065Phenyl-Naphthyl amines
    • 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
    • C10N2010/02Groups 1 or 11
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention relates to lubricating greases. It relates particularly to lubricating greases having excellent structural stability to mechanical working over long periods of time when thickened with relatively small amounts of soap.
  • an improved lubricating grease having improved structural stability and freedom from syneresis may be made b combining with the alkali metal soaps of high and low molecular weight fatty acids a soap of an aryl-aliphatic acid.
  • these improved greases are obtained when employing much lesser amounts of soap than are required in the greases of the prior art.
  • the improved lubricating grease of this invention consists essentially, in addition to the lubricating oil from which the grease is made, of three components. These components are:
  • the three soaps present in the grease as listed in the foregoing paragraph may be of the same alkali metal or they may be of different metals. Of the alkali metals, lithium and sodium are preferred. The preferred embodiment also contemplates that the three soap components be of the same alkali metal.
  • the high molecular weight fatty acid of component (1) may be any of the ordinary fatty acids used in grease making. Among a list of these will be found stearic acid, hydroxy-stearic acid, hy-
  • drogenated fish oil acids beef fat acids, tallow acids, the saturated or unsaturated glycerides of the various fatty acids or mixtures of the above. These acids having a carbon chain length of from 16 to 20 carbon atoms are preferred.
  • acrylonitrile As the low molecular weight acid in compopounds which yield such acids, for example acrylonitrile, may be used.
  • the acid chosen must have an aliphatic chain of at least 8 carbon atoms in length and there must be dependent from that chain an aryl group which may or may not contain substituent groups.
  • These acids may be formed by the Friedel-Crafts condensation of an unsaturated acid and an aryl compound. Using as an example xylyl-stearic acid as a final product, their preparations may be illustrated by the following equation:
  • aryl-aliphatic acid soap the most part it will be desirable to utilize, only minor proportions of the aliphatic-aryl soap component, it being the most expensive of the three soaps. It has been found that with increasing amounts of the aryl-aliphatic acid soap, the final grease product increases in elasticity and cohesiveness. For .optimum results, especially in the case of lithium soap greases, about 0.25% to 2.0% of the aryl-aliphatic acid soap should be used with from 2.25% to 17.0% by weight of the high molecular weight fatty acid soap and from 0.5% to 4.0% of the low molecular weight acid soap. In the case of sodium soap greases, greater amounts of aryl-aliphatic acid may be employed, for example equal to but preferably not greater than the amount of fatty acid employed. The mol ratio of low molecular weight acid to the combined aryl-aliphatic and fatty acids is preferably 1/1 or greater, for example, 2/1 or 3/1.
  • the grease formed was very hard and of an elastic-cohesive nature. Using this grease material as a base, successive additions of the same oil used in the manufacture of the base were made (heating to 500 F. after each addition and cooling to room temperature), thus, in effect, forming a series of greases with decreasing amounts of the xylyl-stearic acid soap contained therein. For convenience in examination the following table gives a chart of these greases and their components along with the properties of the greases so formed:
  • the sodium soap greases containing the xylyl-stearic acid soap shows a slightly higher unworked penetration than does the lithium soap greases (153 mm./ for grease (b) of Example IV compared to 105 mm./10 for grease (a) of Example III). This indicates some slightly lower thickening effect of the sodium soap of the xylyl-stearic acid.
  • the sodium based greases are very satisfactory from the point of view of both structural and thermal stability.
  • this invention comprises an improved lubricating grease which is made by combining with a lubricating oil a mixture of the alkali metal soaps of ,a high molecular weight substantially saturated fatty acid, a low molecular Weight fatty acid and an aryl-aliphatic acid.
  • a lubricating oil a mixture of the alkali metal soaps of ,a high molecular weight substantially saturated fatty acid, a low molecular Weight fatty acid and an aryl-aliphatic acid.
  • the use of the aryl-aliphatic acid soap permits better soap dispersion in the oil and is obviously an economic advantage since it permits the manufacture of a mixed acid base soap grease with excellent structural stability with a smaller proportion of soap than was heretofore believed pos- What is claimed is:
  • An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the alkali metal soaps of a mixture of about 2.25% to 17% by weight of a high molecular weight substantially saturated fatty acid having from 16 to 20 carbon atoms, from about 0.5% to 4.0% by weight of a low molecular weight fatty acid having from 1 to 4 carbon atoms, and about 0.25% to 2% by weight of an aryl-aliphatic acid containing in the aliphatic portion a hydrocarbon chain of from 8 to 20 carbon atoms.
  • An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the alkali metal soaps of a mixture of about 2.25% to 17% by weight of a high molecular weight substantially saturated fatty acid having from 16 to 20 carbon atoms per molecule, from about 0.5% to 4.0% by weight of a low molecular weight fatty acid having from 1 to 4 carbon atoms per molecule, and about 0.25% to 2% by weight of an aryl-aliphatic acid wherein the aliphatic portion contains 17 carbon atoms and the aryl portion is selected from the class consisting of substituted and unsubstituted benzenes.
  • An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with about 4.5% by weight of the lithium soap of hydrogenated fish oil acid, about 1.3% by weight of the lithium soap of a low molecular weight fatty acid having from 1 to 4 carbon atoms per molecule and about 0.5 by weight of the lithium soap of an aryl-aliphatic acid wherein the aliphatic portion contains from 8 to 20 carbon atoms, said weight percents being based on the weight of the total grease composition.
  • An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the sodium soaps of a mixture of acids, said mixture es sentially of equal proportions of an aryl-aliphatic acid wherein the aliphatic portion contains from 8 to 20 carbon atoms and a high molecular weight substantially saturated fatty acid having from 16 to 20 carbon atoms per molecule combined with a low molecular weight fatty acid having from 1 to 4 carbon atoms per molecule, the mol ratio of the low molecular weight fatty acid to the combined aryl-aliphatic acid and high molecular weight acid being within a range of from 1/1 to 3/1.
  • An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the sodium soap of a mixture of acids, said mixture consisting essentially of about 10.0% hydrogenated fish oil acids, about 3.5% acetic acid, and about 10.0% xylyl-stearic acid, said percentages being by weight based on the weight of the total composition.

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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

Patented Feb. 19, 1952 LUBRICATING GREASE Arnold J. Moi-way, Rahway, and Louis A. Mikeska,
Westfield, N. J., assignors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application November 1, 1949, Serial No. 124,941
7 Claims.
This invention relates to lubricating greases. It relates particularly to lubricating greases having excellent structural stability to mechanical working over long periods of time when thickened with relatively small amounts of soap.
Prior art has shown greases thickened with the alkali metal soaps of combinations of high and low molecular weight fatty acids. The art has also shown that in order to obtain the desiredstructural stability and freedom from syneresis, or oil separation, these greases must have a soap content of at least 10%. Even in those cases in which this minimum amount of the mixed soap of low and high molecular weight fatty acids is present, structural stability to oil separation is generally poor.
It has now been found, and comprises the object of this invention, that an improved lubricating grease having improved structural stability and freedom from syneresis may be made b combining with the alkali metal soaps of high and low molecular weight fatty acids a soap of an aryl-aliphatic acid. In certain cases these improved greases are obtained when employing much lesser amounts of soap than are required in the greases of the prior art.
The improved lubricating grease of this invention consists essentially, in addition to the lubricating oil from which the grease is made, of three components. These components are:
(1) An alkali metal soap of a substantially saturated fatty acid of high molecular weight;
(2) An alkali metal salt of a fatty acid of low molecular weight; and
(3) An alkali metal soap of an aryl-aliphatic acid wherein the aliphatic portion has a carbon chain of from 8 to 20 carbon atoms.
The three soaps present in the grease as listed in the foregoing paragraph may be of the same alkali metal or they may be of different metals. Of the alkali metals, lithium and sodium are preferred. The preferred embodiment also contemplates that the three soap components be of the same alkali metal.
The high molecular weight fatty acid of component (1) may be any of the ordinary fatty acids used in grease making. Among a list of these will be found stearic acid, hydroxy-stearic acid, hy-
drogenated fish oil acids, beef fat acids, tallow acids, the saturated or unsaturated glycerides of the various fatty acids or mixtures of the above. These acids having a carbon chain length of from 16 to 20 carbon atoms are preferred.
As the low molecular weight acid in compopounds which yield such acids, for example acrylonitrile, may be used.
There are two requirements outstanding which must be met when choosing the acid for component (3) The acid chosen must have an aliphatic chain of at least 8 carbon atoms in length and there must be dependent from that chain an aryl group which may or may not contain substituent groups. These acids may be formed by the Friedel-Crafts condensation of an unsaturated acid and an aryl compound. Using as an example xylyl-stearic acid as a final product, their preparations may be illustrated by the following equation:
a cnacmpcu=on ompc I on A10]; OH
CH CH3 CH3 CH3 istics of the final grease composition desired. For
the most part it will be desirable to utilize, only minor proportions of the aliphatic-aryl soap component, it being the most expensive of the three soaps. It has been found that with increasing amounts of the aryl-aliphatic acid soap, the final grease product increases in elasticity and cohesiveness. For .optimum results, especially in the case of lithium soap greases, about 0.25% to 2.0% of the aryl-aliphatic acid soap should be used with from 2.25% to 17.0% by weight of the high molecular weight fatty acid soap and from 0.5% to 4.0% of the low molecular weight acid soap. In the case of sodium soap greases, greater amounts of aryl-aliphatic acid may be employed, for example equal to but preferably not greater than the amount of fatty acid employed. The mol ratio of low molecular weight acid to the combined aryl-aliphatic and fatty acids is preferably 1/1 or greater, for example, 2/1 or 3/1.
To more clearly explain the concept of this invention, "the following examples are given.
EXAMPLE 1 A grease composition having the following formulation was prepared:
Percent by weight conventionally refined Coastal distillate having a viscosity at 210 F. of 55 S. U. S 92.7
One-third of the oil, all of the hydrogenated fish oil acids, and the xylyl-stearic acid were charged to a fire-heated grease kettle and heated to 150 F. The acetic acid was then added and the acids co-neutralized with the lithium hydroxide dissolved in boiling water. The temperature was then raised. to 225-250 F. to dehydrate the mixture. After dehydration the balance of the oil was added and the temperature raised to 450-500 F. The fluid molten grease was then rapidly chilled in thin layers. was then returned to the kettle for homogenization.
This grease was tested in accordance with the ASTM procedure for testing penetration and a test result of 250 mm./l at 77 F. After working for 100,000 strokes in an ASTM worker using the fine hole plate (having 325 1%" holes) the penetration at 77 F. increased only 5 mm./i0 (255 mm./). This indicates an outstanding structure stability. The dropping point of this grease was 370 F. Employing the same formulation as Example I excluding the xylyl stearatc,
The cold grease Inspection tests on this grease composition were as follows:
Dropping point, F., 375
Unworked penetration, 260 mm./10
Worked penetration (100,000 strokes 325 hole worker plate), 347 mm./10
Percent free alkalinity, 0.08 as NaOl-I EXAMPLE III The elfect of the presence of the aryl-aliphatic acid soap upon a grease structure is clearly shown by the following:
According to the method outlined in Example I above a grease with the following formulation was prepared.
Percent by weight Hydrogenated fish oil acids 10.0 Xylyl-stearic acid 10.0 Acetic acid 3.5 Lithium hydroxide monohydrate 5.1 Phenyl alpha naphthylamine 1.0
conventionally refined Coastal distillate having a viscosity at 210 F. of S. U. S. 70.4
The grease formed was very hard and of an elastic-cohesive nature. Using this grease material as a base, successive additions of the same oil used in the manufacture of the base were made (heating to 500 F. after each addition and cooling to room temperature), thus, in effect, forming a series of greases with decreasing amounts of the xylyl-stearic acid soap contained therein. For convenience in examination the following table gives a chart of these greases and their components along with the properties of the greases so formed:
Table I PROPERTIES OF GREASE STRUCTURES CONTAINING ARYL-ALIPHATIO ACID the product is soft and structurally unstable both to mechanical working and oil separation.
EXAMPLE II A similar grease was prepared employing a mixture of acrylic acid and acetic acid as the low molecular weight constituent:
Percent by weight Acrylonitrile 0.65 Acetic acid 0.50 Xylyl-stearic acid 0.50 Hydrogenated fish oil acid 4.50 Lithium hydroxide monohydrate 1.40
Conventionally refined Coastal distillate having a viscosity at 210 F. of 55 S. U. S- 91.95 Phenyl alpha naphthylamine (oxidation inhibitor) 0.50
The data reported in Table I above shows that reduction of the xylyl-stearic acid content Ivduced the elastic-cohesive nature of the grease structure. It also shows that excessive amounts of the xylyl lithium stearate in combination with lithium aliphatic acid soaps will give products generally unsuitable due to excessive elasticity and cohesiveness. It also shows that greases having stable structures may be obtained with extremely small amounts of soap thickener pres ent, with the elastic cohesive nature practically eliminated in the lower soap content products.
EXAMPLE IV Using sodium hydroxide to form the acid soaps, and following the procedure outlined in Example I above, greases having the following formulation were made:
Per Cent by Weight Xylyl-stearic acid 20. 10.0 Hydrogenated fish oil acid 10.0 Acetic acid 3.0 3. Sodium hydroxide 4. 8 5.0 Phenyl alpha naphthylamine 1.0 l. 0 conventionally refined Coastal distillate having a viscosity at 210 F. of 55 S. U. S 71. 2 70. 5
These sodium soap grease formulations gave the following inspections:-
Properties (a) Per Cent Free Alkalinity (as NaOH) 0.66 0. 34 Unworked Penetration at 77 F. (mm./l0) 179 153 Worked Penetration at 77 F. 63,000 strokes fine hole worker (mm./l0). 195 202 Dropping Point, F 480 496 Physical Appearance 1 Very elastic and cohesive.
1 Smooth, short fiber, good adhesivcness to metal, very slightly cohesive, no tendency to separate oil.
It will be noted that the sodium soap greases containing the xylyl-stearic acid soap shows a slightly higher unworked penetration than does the lithium soap greases (153 mm./ for grease (b) of Example IV compared to 105 mm./10 for grease (a) of Example III). This indicates some slightly lower thickening effect of the sodium soap of the xylyl-stearic acid. However, the sodium based greases are very satisfactory from the point of view of both structural and thermal stability.
To summarize briefly, this invention comprises an improved lubricating grease which is made by combining with a lubricating oil a mixture of the alkali metal soaps of ,a high molecular weight substantially saturated fatty acid, a low molecular Weight fatty acid and an aryl-aliphatic acid. The use of the aryl-aliphatic acid soap permits better soap dispersion in the oil and is obviously an economic advantage since it permits the manufacture of a mixed acid base soap grease with excellent structural stability with a smaller proportion of soap than was heretofore believed pos- What is claimed is:
1. An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the alkali metal soaps of a mixture of about 2.25% to 17% by weight of a high molecular weight substantially saturated fatty acid having from 16 to 20 carbon atoms, from about 0.5% to 4.0% by weight of a low molecular weight fatty acid having from 1 to 4 carbon atoms, and about 0.25% to 2% by weight of an aryl-aliphatic acid containing in the aliphatic portion a hydrocarbon chain of from 8 to 20 carbon atoms.
2. An improved lubricating composition according to claim 1 wherein the alkali metal is lithium.
3. An improved lubricating composition according to claim 1 wherein the alkali metal is sodium.
4. An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the alkali metal soaps of a mixture of about 2.25% to 17% by weight of a high molecular weight substantially saturated fatty acid having from 16 to 20 carbon atoms per molecule, from about 0.5% to 4.0% by weight of a low molecular weight fatty acid having from 1 to 4 carbon atoms per molecule, and about 0.25% to 2% by weight of an aryl-aliphatic acid wherein the aliphatic portion contains 17 carbon atoms and the aryl portion is selected from the class consisting of substituted and unsubstituted benzenes.
5. An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with about 4.5% by weight of the lithium soap of hydrogenated fish oil acid, about 1.3% by weight of the lithium soap of a low molecular weight fatty acid having from 1 to 4 carbon atoms per molecule and about 0.5 by weight of the lithium soap of an aryl-aliphatic acid wherein the aliphatic portion contains from 8 to 20 carbon atoms, said weight percents being based on the weight of the total grease composition.
6. An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the sodium soaps of a mixture of acids, said mixture es sentially of equal proportions of an aryl-aliphatic acid wherein the aliphatic portion contains from 8 to 20 carbon atoms and a high molecular weight substantially saturated fatty acid having from 16 to 20 carbon atoms per molecule combined with a low molecular weight fatty acid having from 1 to 4 carbon atoms per molecule, the mol ratio of the low molecular weight fatty acid to the combined aryl-aliphatic acid and high molecular weight acid being within a range of from 1/1 to 3/1.
7. An improved lubricating composition which comprises a major proportion of a lubricating oil thickened to a grease consistency with the sodium soap of a mixture of acids, said mixture consisting essentially of about 10.0% hydrogenated fish oil acids, about 3.5% acetic acid, and about 10.0% xylyl-stearic acid, said percentages being by weight based on the weight of the total composition.
ARNOLD J. MORWAY. LOUIS A. MIKESKA.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,182,137 Ricketts Dec. 5, 1939 2,197,263 Carmichael et a1. Apr. 6, 1940 2,468,098 Morway et al Apr. 26, 1949 2,468,099 Morway Apr. 26, 1949 2,487,080 Swanson Nov. 8, 1949

Claims (1)

1. AN IMPROVED LUBRICATING COMPOSITION WHICH COMPRISES A MAJOR PROPORTION OF A LUBRICATING OIL THICKENED TO A GREASE CONSISTENCY WITH THE ALKALI METAL SOAPS OF A MIXTURE OF ABOUT 2.25% TO 17% BY WEIGHT OF A HIGH MOLECULAR WEIGHT SUBSTANTIALLY SATURATED FATTY ACID HAVING FROM 16 TO 20 CARBON ATOMS, FROM ABOUT 0.5% TO 4.0% BY WEIGHT OF A LOW MOLECULAR WEIGHT FATTY ACID HAVING FROM 1 TO 4 CARBON ATOMS, AND ABOUT 0.25% TO 2% BY WIGHT OF AN ARYL-ALIPHATIC ACID CONTAINING IN THE ALIPHATIC PORTION A HYDROCARBON CHAIN OF FROM 8 TO 20 CARBON ATOMS.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2612473A (en) * 1951-08-04 1952-09-30 Standard Oil Dev Co Lubricating grease compositions
US2712527A (en) * 1952-08-26 1955-07-05 Exxon Research Engineering Co Improved lubricating greases containing dihydroxy stearic acid soap
US2750341A (en) * 1951-12-28 1956-06-12 Exxon Research Engineering Co Lubricating grease comprising a synthetic oil and a complex thickener
US2801974A (en) * 1952-12-22 1957-08-06 Exxon Research Engineering Co Grease process utilizing the alkali fusion products of cyclic alcohols
US2953528A (en) * 1957-06-17 1960-09-20 Texaco Inc Lubricating grease thickened with lithium soap of styrenated fatty acid

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2182137A (en) * 1937-02-01 1939-12-05 Shell Dev Soda soap grease
US2197263A (en) * 1939-02-23 1940-04-16 Socony Vacuum Oil Co Inc Grease composition
US2468099A (en) * 1947-10-01 1949-04-26 Standard Oil Dev Co High-temperature grease
US2468098A (en) * 1948-02-18 1949-04-26 Standard Oil Dev Co Grease composition
US2487080A (en) * 1947-11-28 1949-11-08 Standard Oil Co Grease

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2182137A (en) * 1937-02-01 1939-12-05 Shell Dev Soda soap grease
US2197263A (en) * 1939-02-23 1940-04-16 Socony Vacuum Oil Co Inc Grease composition
US2468099A (en) * 1947-10-01 1949-04-26 Standard Oil Dev Co High-temperature grease
US2487080A (en) * 1947-11-28 1949-11-08 Standard Oil Co Grease
US2468098A (en) * 1948-02-18 1949-04-26 Standard Oil Dev Co Grease composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2612473A (en) * 1951-08-04 1952-09-30 Standard Oil Dev Co Lubricating grease compositions
US2750341A (en) * 1951-12-28 1956-06-12 Exxon Research Engineering Co Lubricating grease comprising a synthetic oil and a complex thickener
US2712527A (en) * 1952-08-26 1955-07-05 Exxon Research Engineering Co Improved lubricating greases containing dihydroxy stearic acid soap
US2801974A (en) * 1952-12-22 1957-08-06 Exxon Research Engineering Co Grease process utilizing the alkali fusion products of cyclic alcohols
US2953528A (en) * 1957-06-17 1960-09-20 Texaco Inc Lubricating grease thickened with lithium soap of styrenated fatty acid

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