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US3493507A - Grease compositions - Google Patents

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US3493507A
US3493507A US527754A US3493507DA US3493507A US 3493507 A US3493507 A US 3493507A US 527754 A US527754 A US 527754A US 3493507D A US3493507D A US 3493507DA US 3493507 A US3493507 A US 3493507A
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grease
thickening agent
alkyl
lithium
thiophosphate
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US527754A
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Alfred R Haak
John M Tims
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
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    • 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
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    • 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
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/144Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
    • 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
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/146Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings having carboxyl groups bound to carbon atoms of six-membeered aromatic rings having a hydrocarbon substituent 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
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/108Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
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    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/109Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
    • 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/045Metal containing thio derivatives
    • 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
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/08Groups 4 or 14
    • 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
    • C10N2050/10Form in which the lubricant is applied to the material being lubricated semi-solid; greasy

Definitions

  • a lubricating grease containing a combination of a thiophosphate, salicylic acid or a metal salt thereof and an alkyl-substituted aryl sulfonic acid or a metal salt thereof forms a nonstaining grease having good extreme pressure properties, wear resistance, oxidation and corrosion resistance.
  • the invention relates to grease compositions, and is particularly concerned with those grease compositions which are thickened with a lithium salt of a fatty acid, more particularly lithium l2-hydroxy-stearate.
  • Greases having good high temperature performance are well known.
  • Such greases comprise a suitable base oil, such as a refined hydrocarbon oil of lubricating grade, a thickening agent such as a fatty acid soap or salt or a non-soap thickening agent, a polar structure modifier for the thickening agent, if necessary, for example glycerol, and conventional additives for improving oxidation re sistance, extreme pressure properties and/or corrosion resistance.
  • Such additives include diaryl amines such as phenyl a-naphylamine for oxidation resistance, metal alkyl or aryl thiophosphates, such as zinc or cadmium dialkyl dithiophosphate for a combination of oxidation resistance and extreme pressure properties, and a metal (e.g., lead) naphthenate for anti-corrosion properties. It has not hitherto been found possible, however, to achieve a completely satisfactory combination of all these properties.
  • a grease composition comprising a base oil; a thickening agent; a metal dialkyl thiophosphate, a metal diaryl thiophosphate, or a metal monoalkyl, monoaryl thiophosphate; salicylic acid or a metal salt thereof; and an oilsoluble alkyl-substituted aryl sulphonic acid or a metal salt thereof.
  • the thickening agent is preferably a lithium salt or soap of a fatty acid, more preferably lithium 12-hydroxy stearate, which is incorporated in the grease in an amount necessary to give the required consistency.
  • a lithium salt or soap of a fatty acid more preferably lithium 12-hydroxy stearate
  • aluminium complex soaps could be used.
  • the amount of lithium 12-hydroxy stearate used is between about 7 and 12% by weight based on the total of base oil plus thickening agent. Preferred amounts are between 9 and 11% but as little as 1% or as much as 15%, by weight based on the total of base oil plus thickening agent can be used in some instances.
  • the corresponding proportion is preferably between 6% and 12% by weight.
  • a polar structure modifier such as glycerol
  • glycerol may be included in the composition in an amount of up to 25 e.g., from 5 to 25% by weight based on the thickening agent or up to 4%, e.g., from 0.5 to 4% by weight based on the total composition.
  • Other polar structure modifiers which may be used include diand poly-hydroxy compounds wherein the hydroxy groups are attached to carbon atoms which are adjacent or separated by not more than one carbon atom.
  • the structure modifiers therefore include a large number of diols or polyalcohols and also ethoxylated derivatives of fatty alcohols, fatty acids, or diols.
  • the metal dialkyl or diaryl thiophosphate is preferably an oil-soluble zinc dialkyl dithiophosphate in which the alkyl groups may be the same or different.
  • Zinc isobutyl/ amyl dithiophosphate and zinc ethyl-isobutyl/isopropyl dithiophosphate are preferred.
  • These thiophosphates are preferably incorporated in amount of from 0.2 to 5.0% by weight based on the total of the base oil plus thickening agent and polar structure modifier (if any).
  • a metal monoalkyl, monoaryl thiophosphate, e.g., zinc isobutyl, phenyl dithiophosphate could be used.
  • the thiophosphate should be fully esterified so that the two hydrocarbyl groups attached to the oxygen atoms in the thiophosphate radical should be either both alkyl or both aryl groups or one an alkyl and the other an aryl group.
  • a salt of salicylic acid is used, more preferably lead salicylate, but other salts such as monoor di-lithium salicylate or free salicylic acid may be used.
  • the preferred amount of salicylic acid or salicylate is from 0.1 to 5.0% by Weight based on the total of base oil plus thickening agent and polar structure modifier (if any), and amounts from 0.25 to 4.0% by weight are particularly preferred.
  • a salt of an oil-soluble alkyl-substituted aryl sulphonic acid is used, more preferably an alkaline earth metal salt of an alkyl-substituted naphthalene sulphonic acid in which the alkyl group or groups each contain from 2 to 22 carbon atoms, in amount of from 0.1 to 5.0% by weight based on the total of base oil plus thickening agent and polar structure modifier (if any).
  • the preferred salts are barium salts but other salts such as calcium or mag nesium sulphonates or alkali metal salts, or the free sulphonic acid or amine salts thereof may be used in equivalent amounts if desired.
  • a grease composition was prepared by mixing, under the normal conditions for preparing such greases well known to those skilled in the art, the following components:
  • Timken load test (Il).Fed. M 791-6505.
  • Tinken wear test (III).Fed. M 79l6505.

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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

United States Patent Oflice 3,493,507 Patented Feb. 3, 1970 3,493,507 GREASE COMPOSITIONS Alfred R. Haak, Mohnwey, Germany, and John M. Tims,
Wantage, England, assignors to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Feb. 16, 1966, Ser. No. 527,754 Claims priority, application Great Britain, Feb. 24, 1965, 8,0 13/ 65 Int. Cl. ClOm 5/24, 5/14, 5/22 US. Cl. 252--32.7 1 Claim ABSTRACT OF THE DllSCLOSURE A lubricating grease containing a combination of a thiophosphate, salicylic acid or a metal salt thereof and an alkyl-substituted aryl sulfonic acid or a metal salt thereof forms a nonstaining grease having good extreme pressure properties, wear resistance, oxidation and corrosion resistance.
The invention relates to grease compositions, and is particularly concerned with those grease compositions which are thickened with a lithium salt of a fatty acid, more particularly lithium l2-hydroxy-stearate.
Greases having good high temperature performance are well known. Such greases comprise a suitable base oil, such as a refined hydrocarbon oil of lubricating grade, a thickening agent such as a fatty acid soap or salt or a non-soap thickening agent, a polar structure modifier for the thickening agent, if necessary, for example glycerol, and conventional additives for improving oxidation re sistance, extreme pressure properties and/or corrosion resistance. Such additives include diaryl amines such as phenyl a-naphylamine for oxidation resistance, metal alkyl or aryl thiophosphates, such as zinc or cadmium dialkyl dithiophosphate for a combination of oxidation resistance and extreme pressure properties, and a metal (e.g., lead) naphthenate for anti-corrosion properties. It has not hitherto been found possible, however, to achieve a completely satisfactory combination of all these properties.
It is an object of the present invention to provide a grease having good high temperature performance, good extreme-pressure properties, good rust inhibition and good wear resisting properties. It is also an object of the invention to provide such a grease which does not stain new paint surfaces.
According to the present invention, there is provided a grease composition comprising a base oil; a thickening agent; a metal dialkyl thiophosphate, a metal diaryl thiophosphate, or a metal monoalkyl, monoaryl thiophosphate; salicylic acid or a metal salt thereof; and an oilsoluble alkyl-substituted aryl sulphonic acid or a metal salt thereof.
The thickening agent is preferably a lithium salt or soap of a fatty acid, more preferably lithium 12-hydroxy stearate, which is incorporated in the grease in an amount necessary to give the required consistency. Alternatively as thickening agent, aluminium complex soaps could be used. Normally, the amount of lithium 12-hydroxy stearate used is between about 7 and 12% by weight based on the total of base oil plus thickening agent. Preferred amounts are between 9 and 11% but as little as 1% or as much as 15%, by weight based on the total of base oil plus thickening agent can be used in some instances. With an aluminium complex the corresponding proportion is preferably between 6% and 12% by weight. Optionally, a polar structure modifier such as glycerol, may be included in the composition in an amount of up to 25 e.g., from 5 to 25% by weight based on the thickening agent or up to 4%, e.g., from 0.5 to 4% by weight based on the total composition. Other polar structure modifiers which may be used include diand poly-hydroxy compounds wherein the hydroxy groups are attached to carbon atoms which are adjacent or separated by not more than one carbon atom. The structure modifiers therefore include a large number of diols or polyalcohols and also ethoxylated derivatives of fatty alcohols, fatty acids, or diols.
The metal dialkyl or diaryl thiophosphate is preferably an oil-soluble zinc dialkyl dithiophosphate in which the alkyl groups may be the same or different. Zinc isobutyl/ amyl dithiophosphate and zinc ethyl-isobutyl/isopropyl dithiophosphate are preferred. These thiophosphates are preferably incorporated in amount of from 0.2 to 5.0% by weight based on the total of the base oil plus thickening agent and polar structure modifier (if any). As an alternative to a dialkyl or diaryl thiophosphate, a metal monoalkyl, monoaryl thiophosphate, e.g., zinc isobutyl, phenyl dithiophosphate could be used. The thiophosphate should be fully esterified so that the two hydrocarbyl groups attached to the oxygen atoms in the thiophosphate radical should be either both alkyl or both aryl groups or one an alkyl and the other an aryl group.
In the preferred embodiment of this invention a salt of salicylic acid is used, more preferably lead salicylate, but other salts such as monoor di-lithium salicylate or free salicylic acid may be used. The preferred amount of salicylic acid or salicylate is from 0.1 to 5.0% by Weight based on the total of base oil plus thickening agent and polar structure modifier (if any), and amounts from 0.25 to 4.0% by weight are particularly preferred.
Preferably a salt of an oil-soluble alkyl-substituted aryl sulphonic acid is used, more preferably an alkaline earth metal salt of an alkyl-substituted naphthalene sulphonic acid in which the alkyl group or groups each contain from 2 to 22 carbon atoms, in amount of from 0.1 to 5.0% by weight based on the total of base oil plus thickening agent and polar structure modifier (if any). The preferred salts are barium salts but other salts such as calcium or mag nesium sulphonates or alkali metal salts, or the free sulphonic acid or amine salts thereof may be used in equivalent amounts if desired.
In order to show the nature and advantages of the invention more clearly a number of examples of the invention will now be described.
A grease composition was prepared by mixing, under the normal conditions for preparing such greases well known to those skilled in the art, the following components:
Parts by weight Hydroxystearic acid 10.00 Lithium hydroxide (LiOH.H O) 1.43 Base oil 87.57 Glycerol 1.00
A solvent extracted naphthenic hydrocarbon oil having a viscosity of 450 S.S.U. at F.
There was thus obtained a grease thickened with approximately 10% by weight of lithium 12-hydroxystearate.
To this grease were added various amounts of (A) a zinc dialkyldithiophosphate in which one of the tWo alkyl groups was an isobutyl group while the other was an amyl group (B) lead salicylate, and (C) barium di-(nonyl naphthalene sulphonate), and the compositions thus obtained were subjected to the following tests:
Oxidation test (I ).-ASTM method D942. Pressure drop measured after 100 hours.
Timken load test (Il).Fed. M 791-6505.
Tinken wear test (III).Fed. M 79l6505.
EMCOR corrosion test (IV).DIN method 51802. Corrosion measured after 7 days and in certain cases after 12 and 21 days.
3 SKF high temperature (V).DIN method 51806 extended to 28 days.
The following table lists the results of these tests:
consisting of lithium salicylate, lead salicylate and salicylic acid, and alkaline earth metal dialkyl naphthalene sultonate.
Wt. percent of additive I II III IV V (A) (B) (C) p.s.i. lb. mg. Days Rating C. Cage wreralagr, 013221111;
3 7 3 110 2, 450 4 0.3 7 2-3 110 700 3 0.3 7 2-3 120 500 2-3 1.0 7 2-3 120 400 2-3 1.5 7 3 120 400 2-3 1. s 7 3 120 400 2-3 2.0 7 3 120 400 2-3 0. 2 7 2-3 110 1, 400 3-4 3 7 2-3 120 760 3 4 7 3 120 600 3 7 1 110 2, 000 4 3. 21 0.1 110 2, 000 4 3 21 0 110 2,000 4 16 21 0 110 2,000 4 3 0.1 7 2 130 150 2-3 3 7 7 2 130 100 2-3 2 7 7 2 130 2-3 1 7 2 130 2 1 7 2-3 130 1-2 1 7 2-3 130 fail 0. 5 50 1 21 0 140 tail 1 Below 100. 2 Fail scoring. 3 Below 1.
References Cited It is apparent from the table of results that, although UNITED STATES A TS the use of a Zinc dialkyl dithiophosphate alone gives good 2 549 6/1958 Reeves et a1 extreme pressure properties and wear resistance, good 2944970 7/1960 Peterson 252 18 oxidation and corrosion resistance and high temperature 3015623 1/1962 Loring 252 18 properties are only developed when a salicylate and an 3:075:005 1/1963 Garden at t 252 33 alkyl aryl sulphonate ar a dfi These results are 2,364,283 12/1944 Freuler 25232.7 markable in that the combined eifects of the three ad- 2,951,803 9/1960 N t t 1 252 1g ditives are achieved without any adverse effects on the 3,203,897 8/1965 Ambrose et al 25232.7 other properties of the grease. In addition the grease 40 OTHER REFERENCES formulation containing all three additives is nonstaining to new paint surfaces on automobile bodies and similar articles.
What is claimed is:
1. A grease composition comprising mineral base oil thickened with lithium 12-l1ydroxy sterate and containing synergistic proportions of zinc dihydrocarbyl dithiophosphate, a salicylic acid component selected from the group Rust Preventive Abilities of Greases and Their Improvement, by Calhoun et al. in Lubrication Engineering, July, 1963, pp. 292-296.
DANIEL E. WYMAN, Primary Examiner I. VAUGHN, Assistant Examiner US. Cl. X.R. 25233
US527754A 1965-02-24 1966-02-16 Grease compositions Expired - Lifetime US3493507A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3981810A (en) * 1975-11-11 1976-09-21 The United States Of America As Represented By The Secretary Of The Navy Grease composition
US5672572A (en) * 1993-05-27 1997-09-30 Arai; Katsuya Lubricating oil composition
US20050197260A1 (en) * 2004-02-05 2005-09-08 Montana State University Environmentally friendly grease composition

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JPS6346299A (en) * 1986-01-16 1988-02-27 Ntn Toyo Bearing Co Ltd Grease for constant speed joint
US4822505A (en) * 1987-07-31 1989-04-18 Exxon Research And Engineering Company Load-carrying grease
JP3402407B2 (en) * 1994-10-05 2003-05-06 昭和シェル石油株式会社 Grease for tripod type constant velocity joint

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US2364283A (en) * 1941-10-21 1944-12-05 Union Oil Co Modified lubricating oil
US2837549A (en) * 1955-05-12 1958-06-03 American Cyanamid Co Zinc dialkyl dithiophosphates
US2944970A (en) * 1954-07-12 1960-07-12 Shell Oil Co High temperature grease compositions containing salicylic acid derivatives
US2951808A (en) * 1957-12-31 1960-09-06 Exxon Research Engineering Co Lubricant compositions containing metal salts of aromatic hydroxy carboxylic acids as antioxidants
US3015623A (en) * 1960-06-24 1962-01-02 Sinclair Refining Co Lithium base grease containing lead oleate, sulfurized lard oil and molybdenum disulfide
US3075005A (en) * 1959-10-05 1963-01-22 Continental Oil Co Production of dinonylnaphthalene sulfonates
US3203897A (en) * 1962-09-20 1965-08-31 Gulf Research Development Co Sodium soap grease containing a zinc salt of a dialkyl dithiophosphate

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US2364283A (en) * 1941-10-21 1944-12-05 Union Oil Co Modified lubricating oil
US2944970A (en) * 1954-07-12 1960-07-12 Shell Oil Co High temperature grease compositions containing salicylic acid derivatives
US2837549A (en) * 1955-05-12 1958-06-03 American Cyanamid Co Zinc dialkyl dithiophosphates
US2951808A (en) * 1957-12-31 1960-09-06 Exxon Research Engineering Co Lubricant compositions containing metal salts of aromatic hydroxy carboxylic acids as antioxidants
US3075005A (en) * 1959-10-05 1963-01-22 Continental Oil Co Production of dinonylnaphthalene sulfonates
US3015623A (en) * 1960-06-24 1962-01-02 Sinclair Refining Co Lithium base grease containing lead oleate, sulfurized lard oil and molybdenum disulfide
US3203897A (en) * 1962-09-20 1965-08-31 Gulf Research Development Co Sodium soap grease containing a zinc salt of a dialkyl dithiophosphate

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3981810A (en) * 1975-11-11 1976-09-21 The United States Of America As Represented By The Secretary Of The Navy Grease composition
US5672572A (en) * 1993-05-27 1997-09-30 Arai; Katsuya Lubricating oil composition
US20050197260A1 (en) * 2004-02-05 2005-09-08 Montana State University Environmentally friendly grease composition

Also Published As

Publication number Publication date
GB1089463A (en) 1967-11-01
DE1594427A1 (en) 1969-05-22

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