US2586693A - Lubricating grease - Google Patents
Lubricating grease Download PDFInfo
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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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- Prior art keywords
- acid
- grease
- soap
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- carbon atoms
- Prior art date
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- Expired - Lifetime
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- 239000004519 grease Substances 0.000 title claims description 35
- 230000001050 lubricating effect Effects 0.000 title claims description 15
- 239000000344 soap Substances 0.000 claims description 43
- 239000002253 acid Substances 0.000 claims description 40
- 239000000203 mixture Substances 0.000 claims description 29
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 17
- 229930195729 fatty acid Natural products 0.000 claims description 17
- 150000004665 fatty acids Chemical class 0.000 claims description 17
- 229910052783 alkali metal Inorganic materials 0.000 claims description 14
- 150000001340 alkali metals Chemical class 0.000 claims description 13
- 239000010687 lubricating oil Substances 0.000 claims description 8
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 125000004432 carbon atom Chemical group C* 0.000 description 14
- 150000007513 acids Chemical class 0.000 description 12
- HWKILGJHKYLMHJ-UHFFFAOYSA-N 2-(2,3-dimethylphenyl)octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C(O)=O)C1=CC=CC(C)=C1C HWKILGJHKYLMHJ-UHFFFAOYSA-N 0.000 description 10
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 229910052744 lithium Inorganic materials 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 7
- 235000021323 fish oil Nutrition 0.000 description 7
- 230000035515 penetration Effects 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 3
- -1 alkali metal salt Chemical class 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 2
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003760 tallow Chemical class 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms 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
- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
-
- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/124—Carboxylix 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
-
- 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/22—Acids obtained from polymerised unsaturated 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
- 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
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-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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US124941A US2586693A (en) | 1949-11-01 | 1949-11-01 | Lubricating grease |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US124941A US2586693A (en) | 1949-11-01 | 1949-11-01 | Lubricating grease |
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US2586693A true US2586693A (en) | 1952-02-19 |
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US124941A Expired - Lifetime US2586693A (en) | 1949-11-01 | 1949-11-01 | Lubricating grease |
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Cited By (5)
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)
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 |
-
1949
- 1949-11-01 US US124941A patent/US2586693A/en not_active Expired - Lifetime
Patent Citations (5)
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)
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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