US3245909A - Lubricating composition - Google Patents
Lubricating composition Download PDFInfo
- Publication number
- US3245909A US3245909A US324205A US32420563A US3245909A US 3245909 A US3245909 A US 3245909A US 324205 A US324205 A US 324205A US 32420563 A US32420563 A US 32420563A US 3245909 A US3245909 A US 3245909A
- Authority
- US
- United States
- Prior art keywords
- lubricating
- corrosion
- compositions
- detergent
- corrosive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 230000001050 lubricating effect Effects 0.000 title claims description 12
- 239000000203 mixture Substances 0.000 title description 27
- 230000007797 corrosion Effects 0.000 claims description 20
- 238000005260 corrosion Methods 0.000 claims description 20
- 239000003599 detergent Substances 0.000 claims description 17
- 239000000314 lubricant Substances 0.000 claims description 14
- 239000010687 lubricating oil Substances 0.000 claims description 10
- 239000003921 oil Substances 0.000 claims description 7
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 6
- 229960002317 succinimide Drugs 0.000 claims description 4
- YVWBQGFBSVLPIK-UHFFFAOYSA-N cyclohex-2-ene-1-carboxylic acid Chemical compound OC(=O)C1CCCC=C1 YVWBQGFBSVLPIK-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 description 16
- UIAFKZKHHVMJGS-UHFFFAOYSA-N 2,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1O UIAFKZKHHVMJGS-UHFFFAOYSA-N 0.000 description 15
- 239000003112 inhibitor Substances 0.000 description 14
- -1 amine compounds Chemical class 0.000 description 9
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 8
- 229940114055 beta-resorcylic acid Drugs 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229940014800 succinic anhydride Drugs 0.000 description 4
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 239000002199 base oil Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 230000003749 cleanliness Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 description 1
- JWOLVTCKNXRZOD-UHFFFAOYSA-N 2-phenylcyclohexa-2,4-diene-1,1-dicarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CC=CC=C1C1=CC=CC=C1 JWOLVTCKNXRZOD-UHFFFAOYSA-N 0.000 description 1
- YAXXOCZAXKLLCV-UHFFFAOYSA-N 3-dodecyloxolane-2,5-dione Chemical class CCCCCCCCCCCCC1CC(=O)OC1=O YAXXOCZAXKLLCV-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910002065 alloy metal Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 230000003137 locomotive effect Effects 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003504 terephthalic acids Chemical class 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Images
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/024—Propene
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- 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
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/141—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings monocarboxylic
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- 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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
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- 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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
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- 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
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
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- 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
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/044—Polyamides
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/045—Polyureas; Polyurethanes
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/02—Esters of silicic acids
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol-fuelled engines
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
Definitions
- This invention relates to novel lubricating compositions. More particularly, it relates to lubricant compositions having superior non-corrosive and non-deposit forming properties.
- Lubricating oils under normal operating conditions, generally undergo oxidative deterioration resulting in the production of substances highly corrosive to metal parts of modern engine and like machinery. Particularly susceptible to such corrosion are the alloy metal (usually copper-lead) bearings employed in todays internal combustion engines.
- a new and superior lubricating composition having excellent non-corrosive and non-deposit forming characteristics can be prepared from a major proportion of an oil of lubricating viscosity in combination with a high molecular weight nitrogen-containing detergent type additive, said combination being corrosive to metal surfaces in normal use, and a minor portion sufficient to inhibit corrosion of 2,-4-dihydroxy benzoic acid.
- novel lubricating compositions of this invention are characterized by remarkable corrosion inhibiting properties over extended operational periods and by greatly improved lubricating of bearings and other sliding surfaces.
- An outstanding advantage of the particular inhibitor lies in the fact that its addition results in no increase in the deposit-forming characteristics of the compositions, a result common with the inhibitors of the prior art.
- of particular advantage is the ability of these compositions to provide superior lubrication for particular bearings such as silver-containing bearings without the usually concommitant tendency to form underhead deposits in such heavy duty diesel service.
- the detergent additive is obtained by heating an alkenyl succinic anhydride with at least 0.5 mole of an amine.
- the substituted succinic anhydrides contemplated as reactants in the process can be readily obtained by heating maleic anhydride with a high molecular weight olefin or with a chlorinated high molecular weight olefin at a temperature from about -200 C.
- Typical high molecular weight olefins which can be employed are polyethylene, polypropylene, polyisobutylene, etc. Polyisobutylene is preferred.
- Suitable polyamine reactants are ethylenediamine, diethylene triamine, tetrae thylene pentamine, and the like. Tetraethylene pentamine is a preferred polyamine reactant.
- a preferred embodiment of the detergent additive is the product obtained by heating one mole of a polyisobutenyl succinic anhydride having about 65 carbon atoms in the olefin chain with 0.9 mole of tetraethylene pentamine.
- the detergent additive is employed in the lubricant composition in an amount sufiicient to impart detergency. Generally, amounts from 0.1 to 10% by weight are preferred.
- the inhibitor of this invention is employed in an amount suflicient to inhibit corrosion. In general, amounts up -to about 1.0% by weight are sufficient. A preferred range for most lubricant compositions is from about 0.01% to about 0.5% by weight.
- any of the well-known types of lubricating oils can be used as the base oils for the compositions of this invention. These oils are corrosive to metal surfaces under normal operating conditions.
- base oils are naphthenic base, parafiin base, and mixed base mineral oils; synthetic oils, for example, alkylene polymers, such as polymers of propylene, butylene, etc., and mixtures thereof; alkylene oxide type polymers; dicarboxylic acid esters; phosphorous esters; silicon esters such as silicates and polysiloxanes; and alkyl aromatic hydrocarbons.
- the corrosion inhibitor of this invention is effective in lubricant compositions containing additional conventional additives such as oxidation inparatfinic neutral oil of SAE 30 grade.
- hibitors include detergents or dispersants, sludge inhibitors, pour depressants, V.I. improvers, antifoaming agents, rust inhibitors, oiliness agents, Wear inhibitors, dyes, etc.
- the 2,4-dihydroxybenzoic acid corrosion inhibitor of this invention may be prepared by any suitable method and is commercially available, often being sold under the name resorcylic acid.
- EXAMPLE I 0.15% by weight of 2,4-dihydroxybenzoic acid was added to a lubricating composition comprising 3.0% by weight of a polybutenyl succinirnide detergent type additive in a lubricating oil base which was a solvent refined
- the detergent was prepared by heating 1 mole of polybutenyl succinic anhydride having about 65 carbon atoms in the alkenyl chain with 0.9 mole of tetraethylene pentamine.
- the lubricant composition prepared in Example I was subjected to the L4 Engine Test and compared with a sample of base oil containing the same detergent and with a sample containing 0.15% by weight of terephthalic acid as a corrosion inhibitor.
- the corrosion characteristics of a lubricant composition is determined in a Chevrolet standard 6- cylinder engine. Weighed copper-lead test bearings and new piston rings are installed. The test is run at a constant engine speed at about 3000 r.p.m. under a load of 30 brake horsepower for a period of 36 hours after a runin period of 8 hours. The outlet temperature of the jacket coolant is about 200 F. and the oil sump temperature about 280 F. At the conclusion of the test the engine is disassembled and the pistons are removed and inspected for varnish deposits and rated for cleanliness on a basis of to 10, 10 being perfectly clean. The bearings are weighed to determine total weight loss due to corrosion. Table I describes the results of tests performed comparing the additive of this invention with terephthalic acid.
- a lubricant composition comprising a major portion of an oil of lubricating viscosity in combination with a minor portion of an alkenyl succinimide lubricating oil detergent sufficient to impart detergency, said combination being corrosive to metal surfaces in normal use and a minor portion sufiicient to inhibit corrosion, of 2,4-dihydroxybenzoic acid.
- the lubricant composition of claim 1 wherein the minor portion of an alkenyl succinimide lubricating oil 3.
- the detergent additive is a polybutenyl succinimide prepared from a polybutenyl succinic anhydride having about carbon atoms in the alkenyl chain and tetraalkylene pentamine, said detergent additive being present in an amount of from 0.1% to 10% by weight.
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- Lubricants (AREA)
Description
United States Patent 015 ice 3,245,909 Patented Apr. 12, 1966 3,245,909 LUBRICATING COMPOSITION Warren Lowe, Berkeley, Calif., assignor to Chevron Research Company, a corporation of Delaware No Drawing. Filed Nov. 18, 1963, Ser. No. 324,205 3 Claims. (Cl. 25251.5)
This invention relates to novel lubricating compositions. More particularly, it relates to lubricant compositions having superior non-corrosive and non-deposit forming properties.
Lubricating oils, under normal operating conditions, generally undergo oxidative deterioration resulting in the production of substances highly corrosive to metal parts of modern engine and like machinery. Particularly susceptible to such corrosion are the alloy metal (usually copper-lead) bearings employed in todays internal combustion engines.
Therefore, it is necessary to add to the lubricating oils, substances which act to reduce the corrosive effect upon the metal surfaces. Corrosion inhibitors which have been employed in the past have not been completely satisfactory. A number of additives have been employed that were not highly effective, thus allowing corrosion of the parts sought to be protected. Others, while quite effective initially, are used up rapidly in service and lose their effectiveness.
Another problem of many prior art anticorrodents has been the fact that they could not be combined success fully in compositions with additives commonly used to effect Wear inhibition, sludge inhibition, pour point depression, detergency, etc. Thus, a desirable inhibitor may be combined with these types of additives without adversely aifecting the properties of either the anticorrodent or the other additives.
Furthermore, many known corrosion inhibitors contain active sulfur and are thus undesirable for use with bearings containing silver and similar metals. The use of silver-containing bearings has greatly increased in such classes of engines as marine and locomotive diesels. Thus non-sulfur-containing lubricants possessing anticorrodent properties are especially desirable.
The use of phthalic acids, especially isophthalic and terephthalic acids as corrosion inhibiting components of lubricant compositions is described in Stewart et al. U.S. Patent 2,809,160. These compounds represent highly effective corrosion inhibitors possessing many desirable characteristics such as the ability to be used in combination with numerous classes of both lubricating oil bases and lubricant additives of various types. However, in some applications, when these compounds are combined in lubricating compositions with certain nitrogen-containing detergents, while excellent anticorredent properties are displayed, a decrease in detergent activity often results. Thus their use in this commercially important class of detergent lubricant compositions results in an increase in the amount of varnish and other carbonaceous materials deposited upon piston valves and skirts and in piston ring grooves. These deposits are deleterious to engine operation and their elimination is a highly desirable objective evidenced by numerous advances recently made in producing better detergent-type additives.
It has now been found that a new and superior lubricating composition having excellent non-corrosive and non-deposit forming characteristics can be prepared from a major proportion of an oil of lubricating viscosity in combination with a high molecular weight nitrogen-containing detergent type additive, said combination being corrosive to metal surfaces in normal use, and a minor portion sufficient to inhibit corrosion of 2,-4-dihydroxy benzoic acid.
The novel lubricating compositions of this invention are characterized by remarkable corrosion inhibiting properties over extended operational periods and by greatly improved lubricating of bearings and other sliding surfaces. An outstanding advantage of the particular inhibitor lies in the fact that its addition results in no increase in the deposit-forming characteristics of the compositions, a result common with the inhibitors of the prior art. As noted above, of particular advantage is the ability of these compositions to provide superior lubrication for particular bearings such as silver-containing bearings without the usually concommitant tendency to form underhead deposits in such heavy duty diesel service.
The corrosion inhibiting characteristics of 2,4-dihydroxy benzoic acid are obtained in particular in combination with recently developed nitrogen-containing non-me tallic ashless detergents in lubricating oil compositions. Examples of such detergents are those derived from alkenyl succinic anhydrides having 30 or more carbon atoms in the alkenyl group and amine compounds, such as tetraethylene pentamine, N-aminoethyl piperazine, dimethylaminopropylamine, etc.
The detergent additive is obtained by heating an alkenyl succinic anhydride with at least 0.5 mole of an amine.
The substituted succinic anhydrides contemplated as reactants in the process can be readily obtained by heating maleic anhydride with a high molecular weight olefin or with a chlorinated high molecular weight olefin at a temperature from about -200 C. Typical high molecular weight olefins which can be employed are polyethylene, polypropylene, polyisobutylene, etc. Polyisobutylene is preferred.
Examples of suitable polyamine reactants are ethylenediamine, diethylene triamine, tetrae thylene pentamine, and the like. Tetraethylene pentamine is a preferred polyamine reactant.
A preferred embodiment of the detergent additive is the product obtained by heating one mole of a polyisobutenyl succinic anhydride having about 65 carbon atoms in the olefin chain with 0.9 mole of tetraethylene pentamine.
The detergent additive is employed in the lubricant composition in an amount sufiicient to impart detergency. Generally, amounts from 0.1 to 10% by weight are preferred.
The additives are a class of chemical compounds recognized in the art as possessing the ability to enable a lubricating oil medium to maintain oxidation products, resins, and other insoluble material in suspension or dispersed in the medium. Compositions in which these additives are employed are normally rendered more corrosive probably due to the removal of naturally formed protective films from bearings and other sliding surfaces. Thus, the use of a compatible and efiicient corrosion inhibitor with these types of compounds is especially desirable.
The inhibitor of this invention is employed in an amount suflicient to inhibit corrosion. In general, amounts up -to about 1.0% by weight are sufficient. A preferred range for most lubricant compositions is from about 0.01% to about 0.5% by weight.
Any of the well-known types of lubricating oils can be used as the base oils for the compositions of this invention. These oils are corrosive to metal surfaces under normal operating conditions. Examples of such base oils are naphthenic base, parafiin base, and mixed base mineral oils; synthetic oils, for example, alkylene polymers, such as polymers of propylene, butylene, etc., and mixtures thereof; alkylene oxide type polymers; dicarboxylic acid esters; phosphorous esters; silicon esters such as silicates and polysiloxanes; and alkyl aromatic hydrocarbons.
As previously mentioned, the corrosion inhibitor of this invention is effective in lubricant compositions containing additional conventional additives such as oxidation inparatfinic neutral oil of SAE 30 grade.
hibitors, detergents or dispersants, sludge inhibitors, pour depressants, V.I. improvers, antifoaming agents, rust inhibitors, oiliness agents, Wear inhibitors, dyes, etc.
The 2,4-dihydroxybenzoic acid corrosion inhibitor of this invention may be prepared by any suitable method and is commercially available, often being sold under the name resorcylic acid.
The following example is illustrative of the lubricating compositions of this invention.
EXAMPLE I 0.15% by weight of 2,4-dihydroxybenzoic acid was added to a lubricating composition comprising 3.0% by weight of a polybutenyl succinirnide detergent type additive in a lubricating oil base which was a solvent refined The detergent was prepared by heating 1 mole of polybutenyl succinic anhydride having about 65 carbon atoms in the alkenyl chain with 0.9 mole of tetraethylene pentamine.
In order to demonstrate the efiiectiveness of 2,4-dihydroxybenzoic acid as a non-deposit forming anticorrodent, the lubricant composition prepared in Example I was subjected to the L4 Engine Test and compared with a sample of base oil containing the same detergent and with a sample containing 0.15% by weight of terephthalic acid as a corrosion inhibitor.
In the L4 test, the corrosion characteristics of a lubricant composition is determined in a Chevrolet standard 6- cylinder engine. Weighed copper-lead test bearings and new piston rings are installed. The test is run at a constant engine speed at about 3000 r.p.m. under a load of 30 brake horsepower for a period of 36 hours after a runin period of 8 hours. The outlet temperature of the jacket coolant is about 200 F. and the oil sump temperature about 280 F. At the conclusion of the test the engine is disassembled and the pistons are removed and inspected for varnish deposits and rated for cleanliness on a basis of to 10, 10 being perfectly clean. The bearings are weighed to determine total weight loss due to corrosion. Table I describes the results of tests performed comparing the additive of this invention with terephthalic acid.
Table l L4 ENGINE TEST As shown by the above data, 2,2-biphenyldicarboxylic acid compares favorably with terephthalic acid in its ability to reduce bearing corrosion with this type of lubricant composition. However, its great superiority lies in the fact that it does not contribute to lowering the varnish rating of the engine as does the terephthalic acid. Thus 2,4-dihydroxybenzoic acid provides excellent corrosion inhibition under actual engine operation and aids in maintaining extremely high engine cleanliness ratings.
The L4 Engine Test is more 'fully described in the CRC Handbook, 1946 Edition, Coordinating Research Council, New York, New York.
I claim:
1. A lubricant composition comprising a major portion of an oil of lubricating viscosity in combination with a minor portion of an alkenyl succinimide lubricating oil detergent sufficient to impart detergency, said combination being corrosive to metal surfaces in normal use and a minor portion sufiicient to inhibit corrosion, of 2,4-dihydroxybenzoic acid.
2. The lubricant composition of claim 1 wherein the minor portion of an alkenyl succinimide lubricating oil 3. The lubricant composition of claim 1 wherein the detergent additive is a polybutenyl succinimide prepared from a polybutenyl succinic anhydride having about carbon atoms in the alkenyl chain and tetraalkylene pentamine, said detergent additive being present in an amount of from 0.1% to 10% by weight.
References Cited by the Examiner UNITED STATES PATENTS 1,854,898 4/1932 Gill et al. 252-57 2,194,478 3/1940 Moser et al. 252-57 2,366,074 12/1944 Wasson et al. 252-57 X 2,434,978 1/1948 Zisman et a1 25257 X 2,715,108 8/1955 Francis 252-57 X 2,776,917 1/1957 Shnitzler 252-57 X 2,809,160 10/1957 Stewart et al. 25257 X 2,991,251 7/1961 Rudel et al 25257 X FOREIGN PATENTS 1,254,094 1/1961 France.
612,775 11/1948 Great Britain.
815,050 6/1959 Great Britain.
922,831 4/1963 Great Britain.
DANIEL E. WYMAN, Primary Examiner.
P. P. GARVIN, Assistant Examiner.
Claims (1)
1. A LUBRICANT COMPRISING A MAJOR PORTION OF AN OIL OF LUBRICATING VISCOSITY IN COMBINATION WITH A MINOR PORTION OF AN ALKENYL SUCCINIMIDE LUBRICATING OIL DETERGENT SUFFICIENT TO IMPART DETERGENCY, SAID COMBINATION BEING CORROSIVE TO METAL SUFACES IN NORMAL USE AND A MINOR PORTION SUFFICIENT TO INHIBIT CORROSION, OF 2,4-DIHYDROBENZOIC ACID.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US324205A US3245909A (en) | 1963-11-18 | 1963-11-18 | Lubricating composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US324205A US3245909A (en) | 1963-11-18 | 1963-11-18 | Lubricating composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3245909A true US3245909A (en) | 1966-04-12 |
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| US324205A Expired - Lifetime US3245909A (en) | 1963-11-18 | 1963-11-18 | Lubricating composition |
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Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4107054A (en) * | 1977-06-27 | 1978-08-15 | Continental Oil Company | Lubricating oil compositions |
| US4434066A (en) | 1980-12-30 | 1984-02-28 | Union Carbide Corporation | Water-based energy transmitting fluid compositions |
| US4569777A (en) * | 1985-03-22 | 1986-02-11 | Olin Corporation | Water-based hydraulic fluid compositions containing selected two-component anti-wear agents |
| US4569778A (en) * | 1985-03-22 | 1986-02-11 | Olin Corporation | Water-based hydraulic fluid compositions containing selected two-component anti-wear agents |
| US4569776A (en) * | 1985-03-22 | 1986-02-11 | Olin Corporation | Water-based hydraulic fluid compositions containing selected two-component anti-wear agents |
| US4609406A (en) * | 1984-09-05 | 1986-09-02 | Pennzoil Company | Rust conversion coatings |
| US4945017A (en) * | 1986-07-09 | 1990-07-31 | Pennzoil Products Company | Rust conversion composition |
| US5015507A (en) * | 1986-07-09 | 1991-05-14 | Pennzoil Products Company | Method of converting rusted surface to a durable one |
| US5629434A (en) * | 1992-12-17 | 1997-05-13 | Exxon Chemical Patents Inc | Functionalization of polymers based on Koch chemistry and derivatives thereof |
| US5643859A (en) * | 1992-12-17 | 1997-07-01 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine and secondary of tertiary amines |
| US5646332A (en) * | 1992-12-17 | 1997-07-08 | Exxon Chemical Patents Inc. | Batch Koch carbonylation process |
| US5650536A (en) * | 1992-12-17 | 1997-07-22 | Exxon Chemical Patents Inc. | Continuous process for production of functionalized olefins |
| US5767046A (en) * | 1994-06-17 | 1998-06-16 | Exxon Chemical Company | Functionalized additives useful in two-cycle engines |
| US6043199A (en) * | 1997-08-26 | 2000-03-28 | Exxon Research And Engineering Co. | Corrosion inhibiting additive combination for turbine oils |
| WO2012174075A1 (en) | 2011-06-15 | 2012-12-20 | The Lubrizol Corporation | Lubricating composition containing an ester of an aromatic carboxylic acid |
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| US4434066A (en) | 1980-12-30 | 1984-02-28 | Union Carbide Corporation | Water-based energy transmitting fluid compositions |
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| US4569777A (en) * | 1985-03-22 | 1986-02-11 | Olin Corporation | Water-based hydraulic fluid compositions containing selected two-component anti-wear agents |
| US4569778A (en) * | 1985-03-22 | 1986-02-11 | Olin Corporation | Water-based hydraulic fluid compositions containing selected two-component anti-wear agents |
| US4569776A (en) * | 1985-03-22 | 1986-02-11 | Olin Corporation | Water-based hydraulic fluid compositions containing selected two-component anti-wear agents |
| US4945017A (en) * | 1986-07-09 | 1990-07-31 | Pennzoil Products Company | Rust conversion composition |
| US5015507A (en) * | 1986-07-09 | 1991-05-14 | Pennzoil Products Company | Method of converting rusted surface to a durable one |
| US5646332A (en) * | 1992-12-17 | 1997-07-08 | Exxon Chemical Patents Inc. | Batch Koch carbonylation process |
| US5643859A (en) * | 1992-12-17 | 1997-07-01 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine and secondary of tertiary amines |
| US5629434A (en) * | 1992-12-17 | 1997-05-13 | Exxon Chemical Patents Inc | Functionalization of polymers based on Koch chemistry and derivatives thereof |
| US5650536A (en) * | 1992-12-17 | 1997-07-22 | Exxon Chemical Patents Inc. | Continuous process for production of functionalized olefins |
| US5696064A (en) * | 1992-12-17 | 1997-12-09 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
| US5698722A (en) * | 1992-12-17 | 1997-12-16 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
| US5703256A (en) * | 1992-12-17 | 1997-12-30 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
| US5717039A (en) * | 1992-12-17 | 1998-02-10 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
| US5767046A (en) * | 1994-06-17 | 1998-06-16 | Exxon Chemical Company | Functionalized additives useful in two-cycle engines |
| US6043199A (en) * | 1997-08-26 | 2000-03-28 | Exxon Research And Engineering Co. | Corrosion inhibiting additive combination for turbine oils |
| WO2012174075A1 (en) | 2011-06-15 | 2012-12-20 | The Lubrizol Corporation | Lubricating composition containing an ester of an aromatic carboxylic acid |
| US9534187B2 (en) | 2011-06-15 | 2017-01-03 | The Lubrizol Corporation | Lubricating composition containing an ester of an aromatic carboxylic acid |
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