US3926823A - Turbine oil compositions - Google Patents
Turbine oil compositions Download PDFInfo
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- US3926823A US3926823A US512766A US51276674A US3926823A US 3926823 A US3926823 A US 3926823A US 512766 A US512766 A US 512766A US 51276674 A US51276674 A US 51276674A US 3926823 A US3926823 A US 3926823A
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- turbine oil
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- 239000000203 mixture Substances 0.000 title claims abstract description 87
- 239000010723 turbine oil Substances 0.000 title claims abstract description 41
- 239000010687 lubricating oil Substances 0.000 claims abstract description 28
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 26
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims abstract description 20
- 150000002148 esters Chemical class 0.000 claims abstract description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 15
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 15
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 15
- 239000012964 benzotriazole Chemical class 0.000 claims abstract description 14
- 229920001577 copolymer Polymers 0.000 claims abstract description 14
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 claims abstract description 13
- -1 alkenyl succinic anhydride Chemical compound 0.000 claims abstract description 12
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229940014800 succinic anhydride Drugs 0.000 claims abstract description 10
- 150000001565 benzotriazoles Chemical class 0.000 claims abstract description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 6
- 239000011707 mineral Substances 0.000 claims abstract description 6
- 239000004711 α-olefin Substances 0.000 claims abstract 2
- 239000000463 material Substances 0.000 claims description 28
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 22
- 239000000314 lubricant Substances 0.000 claims description 13
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims description 13
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 12
- 150000005673 monoalkenes Chemical class 0.000 claims description 9
- 239000002480 mineral oil Substances 0.000 claims description 5
- 235000010446 mineral oil Nutrition 0.000 claims description 5
- 150000003852 triazoles Chemical class 0.000 claims description 5
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 4
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 3
- 239000002199 base oil Substances 0.000 abstract description 13
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 abstract description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 34
- 238000012360 testing method Methods 0.000 description 24
- 239000003921 oil Substances 0.000 description 15
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000010688 mineral lubricating oil Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000003879 lubricant additive Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 238000013112 stability test Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 241001647090 Ponca Species 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000011436 cob Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- HXQHRUJXQJEGER-UHFFFAOYSA-N 1-methylbenzotriazole Chemical compound C1=CC=C2N(C)N=NC2=C1 HXQHRUJXQJEGER-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- JKXJLONVJLKCNA-UHFFFAOYSA-N [2,3-di(nonyl)phenyl] dihydrogen phosphite Chemical compound CCCCCCCCCC1=CC=CC(OP(O)O)=C1CCCCCCCCC JKXJLONVJLKCNA-UHFFFAOYSA-N 0.000 description 1
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- VCAFTIGPOYBOIC-UHFFFAOYSA-N phenyl dihydrogen phosphite Chemical class OP(O)OC1=CC=CC=C1 VCAFTIGPOYBOIC-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000276 potassium ferrocyanide Substances 0.000 description 1
- PDEDQSAFHNADLV-UHFFFAOYSA-M potassium;disodium;dinitrate;nitrite Chemical compound [Na+].[Na+].[K+].[O-]N=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PDEDQSAFHNADLV-UHFFFAOYSA-M 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000010736 steam turbine oil Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- FEVFLQDDNUQKRY-UHFFFAOYSA-N tris(4-methylphenyl) phosphite Chemical compound C1=CC(C)=CC=C1OP(OC=1C=CC(C)=CC=1)OC1=CC=C(C)C=C1 FEVFLQDDNUQKRY-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
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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
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon only
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/30—Heterocyclic compounds
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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
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/028—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
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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
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
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- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/135—Steam engines or turbines
Definitions
- ABSTRACT Lubricating oil compositions particularly suitable for [21] Appl' 5l2766 use in steam turbines or gas turbines, are disclosed.
- the turbine oil compositions comprise a major [52] US. Cl. 252/499; 252/50; 252/51; amount f a r l r y h i hydroc r n base il 252/5 A; 252/78; 252/79 and aminor, but effective, amount of a combination [51] Int.
- the turbine oil compositions may contain, additionally, a small, but effective, amount of tricresyl
- Field of the Invention The invention is in the field of lubricating oils which are particularly suitable for use in gas turbine engines, including aircraft and automotive, and stationary steam turbine engines.
- lubricant additives which work in mineral lubricating oils or synthetic hydrocarbon lubricating oils.
- the lubricant compositions of our invention work is either steam turbines or gas turbines. They are particularly suitable for use in gas turbines. Because of this, our lubricant compositions provide an important advance in the art.
- the present invention is directed to a lubricating oil composition which comprises a major amount of a mineral or synthetic hydrocarbon base oil and an effective amount of a combination of the following materials: (a) copolymer of N-vinyl-2-pyrrolidone and an oz-olefin; (b) triphenyl phosphite or a trialkylsubstituted phenyl phosphite; (c) benzotriazole or alkyl-substituted benzotriazole.
- the lubricating oil composition contains, additionally, a minor but effective amount of tricresyl phosphate or a partial ester of an alkyl or alkenyl succinic anhydride.
- the lubricating oil compositions of our invention have properties which render them particularly useful in steam or gas turbines.
- the base oil can be a conventionally refined mineral lubricating oil or a synthetic hydrocarbon lubricating oil.
- the mineral lubricating oils are well known to those skilled in the art. Both light viscosity (e.g., pale oils) and heavy viscosity (e. g.. bright stock) oils can be used.
- a complete description of mineral lubricating oils is provided by Nelsons Petroleum Refinery Engineering” (McGraw-Hill. New York, 1958).
- Suitable synthetic hydrocarbon lubricating oils include di-n-long-chain alkaryls. as described hereinafter. linear mono-olefin oligomers. and a composition consisting essentially of di-n-long-chain alkaryls and trialkyl-substituted tetrahydronaphthalenes.
- Linear mono-olefin oligomers which are suitable as lubricating oils, are described in several US. Pat. Nos, e.g., 3,382,291, 3,149,178, and 3,808,134.
- a particularly suitable linear mono-olefin oligomer composition is prepared from a-olefins containing 6 to 16 carbon atoms, more suitably 8 to 12 carbon atoms, and preferably 10 carbon atoms.
- the linear mono-olefin oligomer composition contains at least 50 weight percent, more usually at least 60 weight percent, of materials containing 24 to 60 carbon atoms.
- di-n-long-chain alkaryl refers to materials represented by the formula wherein R and R, are alkyl groups containing from 6 to 18 carbon atoms, more suitably from about 9 to about 15 carbon atoms, and preferably from about 10 to 14 carbon atoms, with the sum of R and R, being from about 20 to about 28 carbon atoms and wherein A and A, are hydrogen or a C, or C alkyl group, but preferaby are hydrogen.
- the preferred di-n-long-chain alkaryl is a di-nalkylbenzene wherein the alkyl group contains from about 10 to about 14 carbon atoms.
- the alkyl groups are substantially straight-chain (thus the term n-alkaryls) wherein, preferably, at least 95 percent of the alkyl substituents are bonded to the benzene nucleus through a secondary carbon atom of the respective alkyl groups. While we prefer the term n-alkaryls," other terms such as linear alkaryls or straight-chain alkaryls are equally descriptive.
- the trialkyl-substituted tetrahydronaphthalenes can be represented by the formula wherein R, and R contain from 1 to about 13 carbon atoms each, with the sum of R and R bei'ng'from' about 6 .to about 14 and R and R contain from 1 to addition, they have approximately the same molecular weight.
- the vinyl-pyrrolidone a-olefin copolymers which are suitable for use in our invention are characterized as being the reaction product of N-vinyl-2-pyrrolidone and 0.5 to 12 moles of an a-olefin containing 8 to 30 carbon atoms, preferably 18 to 22 carbon atoms.
- the materials have a molecular weight of about 2,000 to about 20,000, preferably 7,000 to 12,000. Details on the preparation and properties of the copolymers are provided in US. Pat. Nos. 3,296,134 and 3,423,381, whichpatents are made a part of this disclosure.
- the preferred copolymer is the reaction product of 1 mole of N-vinyl-2-pyrrolidone and 1 mole of a C-20 a-olefin.
- An example of a commercially available preferred copolymer is Ganex V-220, which is available from GAE Corporation, 140 West 51st St., New York, NY. This material has the following physical properties:
- Suitable phosphites include triphenyl phosphite and trialky'l-substituted phenyl phosphites, whereinthe phenyl moiety has 1 or 2 alkylsubstituents, each of which contains 1 to 12 carbon atoms.
- Examples of the latter-named phosphites which are suitable include triphenyl phosphite, tritolyl phosphite, tricresyl phosphite, trihexylphenyl phosphite, tributylphenyl phosphite, and tri( mixed monoand dinonylphenyl) phosphite. Tri-(mixed monoand dinonylphenyl) phosphite is particularly suitable.
- Suitable triazoles include benzotriazole and alkylsubstituted benzotriazoles having 1 or 2 alkyl groups containing 1 to carbon atoms, preferably 1 carbon atom.
- Benzotriazole is available under the trade name Cobratec 99 from Sherwin-Williams Chemical.
- a particularly suitable alkyl-substituted benzotriazole is tolyltriazole. which is available under the trade name Cobratec TT100 from Sherwin-Williams Chemical.
- Suitable partial esters of an alkyl or alkenyl succinic anhydride are the products obtained by the reaction of one molar equivalent of a polyhydric alcohol with two molar equivalents of the anhydride. Structurally, these materials are represented by the formula wherein of the radicals R and R, one is hydrogen and the other is an alkyl or alkenyl group'containing from 8 to 15 carbon atoms and R' is the residue of the polyhydric alcohol which generically may contain oxygen, sulfur, or nitrogen in the chain aswell as ester substituents, and preferably contains from 3 to 6 carbon atoms.
- the integer n represents a number from 1 to 4. In so doing, 11 includes, in the residue, derivatives of diols, triols, and other polyhydroxy compounds.
- a preferred partial ester for use in our invention is represented by the formula wherein of R and R, one represents hydrogen and the other a branched chain dodecenyl group and R" is an alkylene group of 3 to 6 carbon atoms.
- a commercially available partial ester which can be used in our invention is I-Iitec E5 36, available from Edwin Cooper Company, St. Louis, M0.
- the preparation of and additional information concerning these partial esters are provided by US. Pat. No. 3,1 17,091, which is made a part of this disclosure.
- Tricresyl phosphate is a well known chemical, being represented by the formula (C H Me)PO Any high quality, commerically available tricresyl phosphate can be used.
- the balance of the composition is the base lubricating oil, it being understood that other conventional lubricant additives can be included, if desired.
- the test apparatus consists of a test tube (to contain the test sample) which is fitted with vertical watercooled condenser and air-delivery tube extending to within one-eighth inch of the bottom of the test tube.
- the tube is submerged its entire length except for the joint and condenser in a constant temperature bath at test temperature.
- a heat stability test was used to measure Cu-Pb hearing corrosion. Briefly, this test can be described as follows.
- a copper-lead faced steel coupon, l X 3 inches, is cleaned in accordance with the established procedure and weighed. Two hundred milliliters of test sample is placed in a 400 ml tall form beaker. The test coupon is placed in the beaker, which is then covered with a watch glass, and placed in a 250F oven for 96 hours. At the end of the specified period of time, the beaker is removed and allowed to cool. The coupon is removed, washed with hexane, dried, and weighed.
- Base oils X and Y were mineral lubricating oils.
- Base oil X was a bright stock having a viscosity of 155 SSU at 210F
- base oil Y was a pale oil having a viscosity of 170 SSU at 100F.
- Base oil 2" was a synthetic hydrocarbon lubricant consisting essentially of di-n-alkylbenzenes and trialkyl-substituted tetrahydronaphthalenes. The alkyl groups of the di-nalkylbenzenes were predominantly C This base oil contained about percent di-n-alkylbenzenes and about 20 percent trialkyl-substituted tetrahydronaphthalenes. It had the following physical properties:
- centistokes and neutralization number change from original are determined on filtered oil.
- Composition C (which corresponds to the broad aspect of our invention) as compared to Compositions A and B shows (a) better viscosity than A, (b) better neutralization number than A, (0) better corrosion than B, and (d) better Cu-Pb bearings than B.
- Composition D which corresponds to Composition C but contains additionally tricresyl phosphate, shows better overall results than composition C except for deposits.
- Composition E is similar to Composition D except that pale oil has been substituted for the synthetic hydrocarbon oil.
- Composition E shows. better viscosity results but higher deposits.
- Composition F corresponds to Composition E but contains additionally a partial ester. As compared to Composition E, Composition F shows better neutralization number, better RBOT, better Cu-Pb bearings, but higher deposits.
- a turbine oil composition comprising a major amount of a mineral or synthetic hydrocarbon base lubricating oil and the following combination of materials in the amounts specified, as weight percent of total composition:
- Viscosit Change +1.86 13.08 contains from about 0.01 to about 0.15 weight percent g gzff fig f g'zf 3 2 32 of a partial ester of an alkyl or alkenyl succinic anhy- Finui Ne N0, 192 dride, which is represented by the formula: Neut. No. Increase 1.77 +5.35 Corrosion. mgs/coupons Silver +1.9 +3.0 C(OJOH C(O)OH Copper +0.4 +0.3 Steel +1.2 +1.0 R- H H-C-R Magnesium +1.7 +2.1 Aluminum +1.9 +1.7 R' H H- R' Deposits (Filtered) Mg/100 gms.
- the base lubricating oil is a synthetic hydrocarbon lubricant which is selected from the group consisting of di-nlong-chain alkaryls, linear mono-olefin oligomers, and a composition consisting essentially of di-n-long-chain alkaryls and trialkyl-substituted tetrahydronaphthalenes.
- di-n-long-chain alkaryls refers to materials represented by the formula wherein R and R are substantially straight-chain alkyl groups containing from 6 to 18 carbon atoms, with the sum of R and R being from about 20 to about 28 and wherein A and A are hydrogen or a C or C alkyl group.
- linear mono-olefin oligomer refers to materials prepared from a-olefins containing 6 to 16 carbon atoms and which contain at least 50 weight percent of materials containing 24 to 60 carbon atoms
- trialkyl-substituted tetrahydronaphthalene refers to materials represented by the formula wherein R and R are straight-chain alkyl groups containing from 1 to about 13 carbon atoms each, with the sum of R and R being from about 6 to about 14, and wherein R and R, are straight-chain alkyl groups containing from about 1 to about 16 carbon atoms, with the sum of R and R being from about 9 to about 17.
- the turbine oil composition of claim 5 wherein it contains from about l to about weight percent tricresyl phosphate.
- R and R wherein of the radicals R and R, one is hydrogen and the other is an alkyl or alkenyl group containing from 8 to 15 carbon atoms, R" is a residue of a polydric alcohol containing from 3 to 6 carbon atoms, and n is an integer of at least one but less than five.
- a turbine oil composition comprising a major amount of a mineral or synthetic hydrocarbon base lubricating oil and the following combination of materials in the amounts specified, as weight percent of total composition:
- the turbine oil composition of claim 10 wherein it contains from about 3 to about 8 weight percent tricresyl phosphate.
- R and R one represents hydrogen and the other a branched chain dodecenyl group and R" is an alkylene group of 3 to 6 carbon atoms.
- the turbine oil composition of claim 9 wherein the base lubricating oil is a synthetic hydrocarbon lubricant which is selected from the group consisting of di-n-long-chain alkaryls, linear mono-olefin oligomers, and a composition consisting essentially of di-n-longchain alkaryls and trialkyl-substituted tetrahydronaphthalenes, wherein a.
- di-n-long-chain alkaryls refers to materials represented by the formula wherein R and R are straight-chain alkyl groups containing from 1 to about 13 carbon atoms each, with the sum of R and R being from about 6 to about 14; and wherein R and R are straight-chain alkyl groups containing from about 1 to about 16 carbon atoms, with the sum of R and R being from about 9 to about l7.
- the turbine oil composition of claim 14 wherein the base lubricating oil is a composition consisting essentially of di-n-long-chain alkaryls, which are present in an amount of 61 to 92 weight percent, and trialkyl-substituted tetrahydronaphthalenes which are present in an amount of 5 to 30 weight percent.
- the turbine oil composition of claim 13 wherein it containsfrom about 0.04 to about 0.08 weight percent of a partial ester of succinic anhydride which is represented by the formula ent in an amount of 5 to 30 weight percent.
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Abstract
Lubricating oil compositions, particularly suitable for use in steam turbines or gas turbines, are disclosed. The turbine oil compositions comprise a major amount of a mineral or synthetic hydrocarbon base oil and a minor, but effective, amount of a combination of copolymer of N-vinyl-2-pyrrolidone and an Alpha olefin, triphenyl phosphite or a trialkyl-substituted phenyl phosphite, and benzotriazole or alkyl-substituted benzotriazole. The turbine oil compositions may contain, additionally, a small, but effective, amount of tricresyl phosphate or a partial ester of an alkyl or alkenyl succinic anhydride.
Description
United States Patent Dun et al. Dec. 16, 1975 [5 TURBINE OIL COMPOSITIONS 3,790,478 2/1974 Rudston et al 252/499 Inventors: Albert M- Durr; Robefi A. 3,790,481 2/l974 Byford et a1, 252/499 532 both of Ponca Clty Primary Examiner-Delbert E. Gantz Assistant Examiner-I. Vaughn [73] Assignee'. Continental Oil Company, Ponca Attorney, Agent, or FirmBayless E. Rutherford, Jr.
City, Okla. 22 Filed: on. 7, 1974 [57] ABSTRACT Lubricating oil compositions, particularly suitable for [21] Appl' 5l2766 use in steam turbines or gas turbines, are disclosed. The turbine oil compositions comprise a major [52] US. Cl. 252/499; 252/50; 252/51; amount f a r l r y h i hydroc r n base il 252/5 A; 252/78; 252/79 and aminor, but effective, amount of a combination [51] Int. Cl}, ClOM 1/10; ClOM 3/02; C1OM 5/02; of copolymer of N-vinyl-2-pyrrolidone and an a-ole- (110M 7/02 fin, triphenyl phosphite or a trialkyl-substituted phenyl [58] Field of Search 252/499, 50, 515 A 78, phosphite, and benzotriazole or alkyl-substituted ben- 252/79 zotriazole. The turbine oil compositions may contain, additionally, a small, but effective, amount of tricresyl [56] References Cit d phosphate or a partial ester of an alkyl or alkenyl suc- UNITED STATES PATENTS Clmc anhydrlde' 3,778,376 12/1973 Herber 252/499 17 Claims, N0 Drawings TURBINE OIL COMPOSITIONS BACKGROUND 1. Field of the Invention The invention is in the field of lubricating oils which are particularly suitable for use in gas turbine engines, including aircraft and automotive, and stationary steam turbine engines.
2. General Background It is generally recognized that the operating conditions of gas turbine engines expose the lubricant to extreme conditions. In order to be satisfactory, the lubricant must be resistant to oxidation and corrosion at high temperatures. Moreover, the lubricant must be resistant to deposit-formation at high temperatures.
Normally, gas turbine and steam turbine units require different lubricant types, the former synthetic esterbased oils and the latter petroleum oils.
We have found a particular combination of lubricant additives which work in mineral lubricating oils or synthetic hydrocarbon lubricating oils. Furthermore, the lubricant compositions of our invention work is either steam turbines or gas turbines. They are particularly suitable for use in gas turbines. Because of this, our lubricant compositions provide an important advance in the art.
3. Prior Art Each of the lubricant additives used in our lubricant compositions is known to be useful in lubricating oils. However, we have found that certain synergistic relationships are present in the additives which provide improved results in the combinations used. Moreover, we have found that the lubricant compositions of our invention provide superior performance, particularly when compared to commercially available products.
BRIEF SUMMARY OF THE INVENTION Broadly stated, the present invention is directed to a lubricating oil composition which comprises a major amount of a mineral or synthetic hydrocarbon base oil and an effective amount of a combination of the following materials: (a) copolymer of N-vinyl-2-pyrrolidone and an oz-olefin; (b) triphenyl phosphite or a trialkylsubstituted phenyl phosphite; (c) benzotriazole or alkyl-substituted benzotriazole.
In further aspects, the lubricating oil composition contains, additionally, a minor but effective amount of tricresyl phosphate or a partial ester of an alkyl or alkenyl succinic anhydride. The lubricating oil compositions of our invention have properties which render them particularly useful in steam or gas turbines.
MATERIALS USED The base oil can be a conventionally refined mineral lubricating oil or a synthetic hydrocarbon lubricating oil. The mineral lubricating oils are well known to those skilled in the art. Both light viscosity (e.g., pale oils) and heavy viscosity (e. g.. bright stock) oils can be used. A complete description of mineral lubricating oils is provided by Nelsons Petroleum Refinery Engineering" (McGraw-Hill. New York, 1958).
Suitable synthetic hydrocarbon lubricating oils include di-n-long-chain alkaryls. as described hereinafter. linear mono-olefin oligomers. and a composition consisting essentially of di-n-long-chain alkaryls and trialkyl-substituted tetrahydronaphthalenes.
Linear mono-olefin oligomers, which are suitable as lubricating oils, are described in several US. Pat. Nos, e.g., 3,382,291, 3,149,178, and 3,808,134.
A particularly suitable linear mono-olefin oligomer composition is prepared from a-olefins containing 6 to 16 carbon atoms, more suitably 8 to 12 carbon atoms, and preferably 10 carbon atoms. The linear mono-olefin oligomer composition contains at least 50 weight percent, more usually at least 60 weight percent, of materials containing 24 to 60 carbon atoms.
The term di-n-long-chain alkaryl refers to materials represented by the formula wherein R and R, are alkyl groups containing from 6 to 18 carbon atoms, more suitably from about 9 to about 15 carbon atoms, and preferably from about 10 to 14 carbon atoms, with the sum of R and R, being from about 20 to about 28 carbon atoms and wherein A and A, are hydrogen or a C, or C alkyl group, but preferaby are hydrogen.
Thus, the preferred di-n-long-chain alkaryl is a di-nalkylbenzene wherein the alkyl group contains from about 10 to about 14 carbon atoms.
The alkyl groups are substantially straight-chain (thus the term n-alkaryls) wherein, preferably, at least 95 percent of the alkyl substituents are bonded to the benzene nucleus through a secondary carbon atom of the respective alkyl groups. While we prefer the term n-alkaryls," other terms such as linear alkaryls or straight-chain alkaryls are equally descriptive.
A particularly suitable di-n-long-chain alkaryl-trialkyl-substituted tetrahydronaphthalene composition typically contains the following The composition is also characterized as having the following properties:
Viscosity index -1 16 Pour point. F 40 to 80 Molecular weight range 350-526 Preferably 375-480 The di-n-long-chain alkaryls meet the description provided in the foregoing.
The trialkyl-substituted tetrahydronaphthalenes can be represented by the formula wherein R, and R contain from 1 to about 13 carbon atoms each, with the sum of R and R bei'ng'from' about 6 .to about 14 and R and R contain from 1 to addition, they have approximately the same molecular weight.
The vinyl-pyrrolidone a-olefin copolymers which are suitable for use in our invention are characterized as being the reaction product of N-vinyl-2-pyrrolidone and 0.5 to 12 moles of an a-olefin containing 8 to 30 carbon atoms, preferably 18 to 22 carbon atoms. The materials have a molecular weight of about 2,000 to about 20,000, preferably 7,000 to 12,000. Details on the preparation and properties of the copolymers are provided in US. Pat. Nos. 3,296,134 and 3,423,381, whichpatents are made a part of this disclosure. The preferred copolymer is the reaction product of 1 mole of N-vinyl-2-pyrrolidone and 1 mole of a C-20 a-olefin. An example of a commercially available preferred copolymer is Ganex V-220, which is available from GAE Corporation, 140 West 51st St., New York, NY. This material has the following physical properties:
1 Physical Form. 25C waxy solid Relative Viscosity 1) 1.007 Density'(Z) 0.95
, Average Molecular Weight (3) 8.600
, Softening Point 30C MeltingRange (4) Suitable phosphites include triphenyl phosphite and trialky'l-substituted phenyl phosphites, whereinthe phenyl moiety has 1 or 2 alkylsubstituents, each of which contains 1 to 12 carbon atoms. Examples of the latter-named phosphites which are suitable include triphenyl phosphite, tritolyl phosphite, tricresyl phosphite, trihexylphenyl phosphite, tributylphenyl phosphite, and tri( mixed monoand dinonylphenyl) phosphite. Tri-(mixed monoand dinonylphenyl) phosphite is particularly suitable.
Suitable triazoles include benzotriazole and alkylsubstituted benzotriazoles having 1 or 2 alkyl groups containing 1 to carbon atoms, preferably 1 carbon atom. Benzotriazole is available under the trade name Cobratec 99 from Sherwin-Williams Chemical. A particularly suitable alkyl-substituted benzotriazole is tolyltriazole. which is available under the trade name Cobratec TT100 from Sherwin-Williams Chemical.
Suitable partial esters of an alkyl or alkenyl succinic anhydride are the products obtained by the reaction of one molar equivalent of a polyhydric alcohol with two molar equivalents of the anhydride. Structurally, these materials are represented by the formula wherein of the radicals R and R, one is hydrogen and the other is an alkyl or alkenyl group'containing from 8 to 15 carbon atoms and R' is the residue of the polyhydric alcohol which generically may contain oxygen, sulfur, or nitrogen in the chain aswell as ester substituents, and preferably contains from 3 to 6 carbon atoms. The integer n represents a number from 1 to 4. In so doing, 11 includes, in the residue, derivatives of diols, triols, and other polyhydroxy compounds.
A preferred partial ester for use in our invention is represented by the formula wherein of R and R, one represents hydrogen and the other a branched chain dodecenyl group and R" is an alkylene group of 3 to 6 carbon atoms.
A commercially available partial ester which can be used in our invention is I-Iitec E5 36, available from Edwin Cooper Company, St. Louis, M0. The preparation of and additional information concerning these partial esters are provided by US. Pat. No. 3,1 17,091, which is made a part of this disclosure.
Tricresyl phosphate is a well known chemical, being represented by the formula (C H Me)PO Any high quality, commerically available tricresyl phosphate can be used.
AMOUNTS OF MATERIALS USED The amounts of the various materials used in the turbine oil compositions of our invention are shown below, in both suitable and preferred ranges.
*Each material is used in only one aspect of our invention.
As is implied, the balance of the composition is the base lubricating oil, it being understood that other conventional lubricant additives can be included, if desired.
USE OF OTHER MATERIALS IN OUR INVENTION In describing our invention, we have shown only the essential materials which are used therein. It is to be understood that other conventional lubricating oil additives can be used in the composition, if desired. Examples of other such materials include, but are not limited to, antifoam agents, pour point depressants, viscosity and viscosity index improvers, and dyes.
In order to disclose the nature of the present invention still more clearly, the following examples, both illustrative and comparative, will be given. It is to be understood that the invention is not to be limited to the specific conditions or details set forth in these examples except insofar as such limitations are specified in the appended claims.
TEST METHODS The test methods used to evaluate the various compositions, both illustrative and comparative, were the following:
1. Federal Test Method 5308.6 of Standard 791 b. 2. Rotary Bomb Oxidation Test ASTM-D2272 3. ASTM-D-943 Oxidation Test 4. Heat Stability Test Inasmuch as the first three tests are standard, published tests, it is not believed necessary that they be decribed in detail herein.
Since the data from the Federal Test Method 5308.6
was used more consistently, this test will be described in some detail. Usually in this test, the only values obtained are oil viscosity change, acid number change, and the weight loss of the metal test specimens. In addition to these values, we obtained the amount of solids deposited or formed during the test. This value is expressed as milligrams of solids per 100 grams of oil sample. In our opinion, this value is a good indicator of the tendency to cause residues in operation of a turbine, which, in turn, can impair performance.
A description of Federal Test Method 5308.6 follows:
A 100-ml test sample, on which viscosity in centistokes at 100F and neutralization number have been measured, is subjected to a temperature of 347F for a period of 72 hours in the presence of 5 liters of air per hour and polished, cleaned, weighed copper, silver, steel, magnesium, and aluminum coupons held rigidly in a specific arrangement.
The test apparatus consists of a test tube (to contain the test sample) which is fitted with vertical watercooled condenser and air-delivery tube extending to within one-eighth inch of the bottom of the test tube. The tube is submerged its entire length except for the joint and condenser in a constant temperature bath at test temperature.
At the end of the test period specified, these observations and measurements are made and recorded:
a. Condenser deposits (liquid or solid) appearance. b. Viscosity change, viscosity change from original at c. Deposits or solids contained in oil sample, in test cell. and on coupons are collected on a filter paper and their weight determined to the nearest 0.1 mg.
d. Metal coupons are washed and weighed to establish loss or gain to the nearest 0.1 mg.
e. Deposits adhering to test cell after scraping and washing are rated for appearance in vapor, oil-air interface, and bottom of test cell.
A heat stability test was used to measure Cu-Pb hearing corrosion. Briefly, this test can be described as follows.
A copper-lead faced steel coupon, l X 3 inches, is cleaned in accordance with the established procedure and weighed. Two hundred milliliters of test sample is placed in a 400 ml tall form beaker. The test coupon is placed in the beaker, which is then covered with a watch glass, and placed in a 250F oven for 96 hours. At the end of the specified period of time, the beaker is removed and allowed to cool. The coupon is removed, washed with hexane, dried, and weighed.
In the following examples the materials used were as follows. Base oils X and Y were mineral lubricating oils. Base oil X was a bright stock having a viscosity of 155 SSU at 210F, while base oil Y was a pale oil having a viscosity of 170 SSU at 100F. Base oil 2" was a synthetic hydrocarbon lubricant consisting essentially of di-n-alkylbenzenes and trialkyl-substituted tetrahydronaphthalenes. The alkyl groups of the di-nalkylbenzenes were predominantly C This base oil contained about percent di-n-alkylbenzenes and about 20 percent trialkyl-substituted tetrahydronaphthalenes. It had the following physical properties:
Viscosity. centistokes 2l0F 5.06 I00F 29. l 2 -40F 9.169 Viscosity Index I l l Pour Point, F -70 The materials, other than base oils, used in the com position were as follows:
Copolymer Ganex" V-220 Triazole Cobrated 99 Phosphite Uniroyal Chemicals Polygard"- a tri (mixed monoand dinonylphenol phosphite Partial Ester Hitec E-536 Antifoam agent A commercially available silicone The amounts of the various materials used in the compositions tested, stated in weight percent, were as follows:
COMPOSITION NO.
Material A B C D E F Copolymer 0.80 0.40 0.40 0.40 0.40 Triazole 0.02 0.02 0.0; 0.01 0.02 0.02
Phosphite L50 0.75 0.75 0.75 0.75 Antifoam 0.l0 O.l0 0.l0 0.10 0.10 0.10 Tricresyl Phosphate 5.00 5.00 5.00 Partial Ester 0.06
Base Oil X 6.00 6.00 6.00 600 Base Oil Y 93.73 93.67
Base Oil Z 93.08 92.38 92.73 87.73
100F. centistokes and neutralization number change from original are determined on filtered oil.
The results of the tests conducted on the various compositions are shown in the table which follows.
Composition No.
A B C D E F Results: Fl'M 5308.6-72 Hr Vis-CS. 100F-Orig. 34.65 34.57 34.54 33.21 34.90 34.98 Final 49.03 43.05 43.57 40.15 37.31 37.31 Vis. Change 14.38 8.48 9.03 6.94 2.41 2.33 7: Vis. Change 41.5 24.5 26.1 20.9 6.9 6.7 Neut. No.Original 0.0 0.20 0.09 0.09 0.33 0.44 -Final 8.49 4.34 4.88 3.79 7.44 2.60 Neut. No Change 8.49 4.14 4.79 3.70 7.1 l 2.16 Corrosionv Mg/coupon Silver 0.8 +0.2 1.5 0.7 -0.1 +0.2 Copper +0.1 0.6 +0.7 0.8 +1.6 +2.2 Steel +0.1 +1.0 +0.1 +0.2 +0.6 +0.3 Magnesium +0.1 +1.9 +0.1 +0.1 +0.1 +0.1 Aluminum +0.1 +1.0 0.0 0.0 +01 +0.1 Deposits Vapor Med Lt Med LtMed Lt Lt Interface Nil Lt Tr Lt Lt Tr-Lt Filteredmg/100 gms 3.1 9.1 8.2 8.1 279 380 Misc. Results CuPb Brg-96 Hrs at 250 Wt. Chg-Mg/Coupon 33 +285 0.1 0.2 +0.4 +0.1 RBOT at 150C. Minutes 51 74 66 60 1 125 Heat stability test A brief study of the results in the preceding table indicates the following. Composition C (which corresponds to the broad aspect of our invention) as compared to Compositions A and B shows (a) better viscosity than A, (b) better neutralization number than A, (0) better corrosion than B, and (d) better Cu-Pb bearings than B. Composition D which corresponds to Composition C but contains additionally tricresyl phosphate, shows better overall results than composition C except for deposits. Composition E is similar to Composition D except that pale oil has been substituted for the synthetic hydrocarbon oil. As compared to Composition D, Composition E shows. better viscosity results but higher deposits. Composition F corresponds to Composition E but contains additionally a partial ester. As compared to Composition E, Composition F shows better neutralization number, better RBOT, better Cu-Pb bearings, but higher deposits.
For purposes of comparison, we provide below the results of tests on a commercial high temperature oil and a typical steam turbine oil. Both used a mineral oil as the base oil.
commercial high temperature oil gave a good RBOT result, it gave extremely high deposits.
Thus, having described the invention in detail, it will be understood by those skilled in the art that certain variations and modifications may be made without departing from the spirit and scope of the invention as defined herein and in the appended claims.
We claim:
1. A turbine oil composition comprising a major amount of a mineral or synthetic hydrocarbon base lubricating oil and the following combination of materials in the amounts specified, as weight percent of total composition:
a. about 0.1 to about 1.0 copolymer of 1 mole N-vinyl-2-pyrrolidone and 0.5 to 12 moles of an a-olefin containing 8 to carbon atoms;
b. about 0.05 to about 1.5 triphenyl phosphite or trialkyl-substituted phenyl phosphite, wherein the phenyl moiety has 1 or 2 alkyl groups, each of which contains 1 to 12 carbon atoms; and
c. about 0.002 to about 0.1 benzotriazole or alkylsubstituted benzotriazole having 1 or 2 alkyl groups containing 1 to 10 carbon atoms.
2. The turbine oil composition of claim 1 wherein the Commercial T ical High gfg base lubricating oil is a mineral oil. p g e 3. The turbine oil composition of claim 2 wherein it contains from about 1 to about 15 weight percent tri- Results: FTM 5308.672 Hr. cresyl phosphate. Original Viscosity. CS at 100F 31.80 34.87 Final viscosity CS at 33 4795 4. 'ljhe turbine oil composition of claim wherein it Viscosit Change +1.86 13.08 contains from about 0.01 to about 0.15 weight percent g gzff fig f g'zf 3 2 32 of a partial ester of an alkyl or alkenyl succinic anhy- Finui Ne N0, 192 dride, which is represented by the formula: Neut. No. Increase 1.77 +5.35 Corrosion. mgs/coupons Silver +1.9 +3.0 C(OJOH C(O)OH Copper +0.4 +0.3 Steel +1.2 +1.0 R- H H-C-R Magnesium +1.7 +2.1 Aluminum +1.9 +1.7 R' H H- R' Deposits (Filtered) Mg/100 gms. 2.140 1.231 OR" RBOT at liilC-Minutes 4o 4( a Inspection of the test results for the two commercial oils shows that over all they were inferior to all of the compositions tested, including A and B. While the wherein of the radicals R and R, one is hydrogen and the other is an alkyl or alkenyl group containing from 8 to 15 carbon atoms, and R is a residue of a polydric alcohol containing from 3 to 6 carbon atoms and n is an integer of at least one but less than five.
5. The turbine oil composition of claim 1 wherein the base lubricating oil is a synthetic hydrocarbon lubricant which is selected from the group consisting of di-nlong-chain alkaryls, linear mono-olefin oligomers, and a composition consisting essentially of di-n-long-chain alkaryls and trialkyl-substituted tetrahydronaphthalenes. wherein a. the term di-n-long-chain alkaryls refers to materials represented by the formula wherein R and R are substantially straight-chain alkyl groups containing from 6 to 18 carbon atoms, with the sum of R and R being from about 20 to about 28 and wherein A and A are hydrogen or a C or C alkyl group.
b. the term linear mono-olefin oligomer refers to materials prepared from a-olefins containing 6 to 16 carbon atoms and which contain at least 50 weight percent of materials containing 24 to 60 carbon atoms, and c. the term trialkyl-substituted tetrahydronaphthalene refers to materials represented by the formula wherein R and R are straight-chain alkyl groups containing from 1 to about 13 carbon atoms each, with the sum of R and R being from about 6 to about 14, and wherein R and R, are straight-chain alkyl groups containing from about 1 to about 16 carbon atoms, with the sum of R and R being from about 9 to about 17.
6. The turbine oil composition of claim 5 wherein it contains from about l to about weight percent tricresyl phosphate.
7. The turbine oil composition of claim 6 wherein (a) the amount of said copolymer is about 0.2 to about 0.6 weight percent, (b) the amount of said phosphite is about 0.5 to about 1.0 weight percent, and (c) the amount of said triazole is about 0.01 to about 0.04 weight percent.
8. The turbine oil composition of claim 5 wherein it contains from about 0.01 to about 0.15 weight percent of a partial ester of an alkyl or alkenyl succinic anhydride. which is represented by the formula:
10 wherein of the radicals R and R, one is hydrogen and the other is an alkyl or alkenyl group containing from 8 to 15 carbon atoms, R" is a residue of a polydric alcohol containing from 3 to 6 carbon atoms, and n is an integer of at least one but less than five.
9. A turbine oil composition comprising a major amount of a mineral or synthetic hydrocarbon base lubricating oil and the following combination of materials in the amounts specified, as weight percent of total composition:
a. about 0.2 to about 0.6 copolymer of about 1 mole of N-vinyl-2-pyrrolidone and about 1 mole of a C-20 a-olefin;
b. about 0.1 to about 1.0 triphenyl phosphite or tri (mixed monoand dinonylphenyl) phosphite; and
c. about 0.01 to about 0.04 benzotriazole or tolyltriazole.
10. The turbine oil composition of claim 9 wherein the base lubricating oil is a mineral oil.
11. The turbine oil composition of claim 10 wherein it contains from about 3 to about 8 weight percent tricresyl phosphate.
12. The turbine oil composition of claim 11 wherein it contains from about 0.04 to about 0.08 weight percent of a partial ester of succinic anhydride which is represented by the formula:
wherein of R and R one represents hydrogen and the other a branched chain dodecenyl group and R" is an alkylene group of 3 to 6 carbon atoms.
13. The turbine oil composition of claim 9 wherein the base lubricating oil is a synthetic hydrocarbon lubricant which is selected from the group consisting of di-n-long-chain alkaryls, linear mono-olefin oligomers, and a composition consisting essentially of di-n-longchain alkaryls and trialkyl-substituted tetrahydronaphthalenes, wherein a. the term di-n-long-chain alkaryls refers to materials represented by the formula wherein R and R are straight-chain alkyl groups containing from 1 to about 13 carbon atoms each, with the sum of R and R being from about 6 to about 14; and wherein R and R are straight-chain alkyl groups containing from about 1 to about 16 carbon atoms, with the sum of R and R being from about 9 to about l7.
14. The turbine oil compositions of claim 13 wherein it contains from about 3 to about 8 weight percent tricresyl phosphate.
15. The turbine oil composition of claim 14 wherein the base lubricating oil is a composition consisting essentially of di-n-long-chain alkaryls, which are present in an amount of 61 to 92 weight percent, and trialkyl-substituted tetrahydronaphthalenes which are present in an amount of 5 to 30 weight percent.
12 16. The turbine oil composition of claim 13 wherein it containsfrom about 0.04 to about 0.08 weight percent of a partial ester of succinic anhydride which is represented by the formula ent in an amount of 5 to 30 weight percent.
Claims (17)
1. A TURBINE OIL COMPOSITION COMPRISING A MAJOR AMOUNT OF A MINERAL OR SYNTHETIC HYDROCARBON BASE LUBRICATING OIL AND THE FOLLOWING COMBINATION OF MATERIALS IN THE AMOUNTS SEPCIFIED, AS WEIGHT PERCENT OF TOTAL COMPOSITION: A. ABOUT 0.1 TO ABOUT 1.0 - COPOLYMER OF 1 MOLE N-VINYL-2PYRROLIDONE AND 0.5 TO 12 MOLES OF AN A-OLEFIN CONTAINING 8 TO 30 CARBON ATOMS; B. ABOUT 0.05 TO ABOUT 1.5 - TRIPHENYL PHOSPHITE OR TRIALKYLSUBSTITUTED PHENYL PHOSPHITE, WHEREIN THE PHENYL MOIETY HAS 1 OR 2 ALKYL GROUPS, EACH OF WHICH CONTAINS 1 TO 12 CARBON ATOMS; AND C. ABOUT 0.002 TO ABOUT 0.1 - BENZOTRIAZOLE OR ALKYL-SUBSTITUTED BENZOTRIAZOLE HAVING 1 OT 2 ALKYL GROUPS CONTAINING 1 TO 10 CARBON ATOMS.
2. The turbine oil composition of claim 1 wherein the base lubricating oil is a mineral oil.
3. THE TURBINE OIL COMPOSITION OF CLAIM 2 WHEREIN IT CONTAINS FROM ABOUT 1 TO ABOUT 15 WEIGHT PERCENT TRICRESYL PHOSPHATE.
4. The turbine oil composition of claim 2 wherein it contains from about 0.01 to about 0.15 weight percent of a partial ester of an alkyl or alkenyl succinic anhydride, which is represented by the formula:
5. The turbine oil composition of claim 1 wherein the base lubricating oil is a synthetic hydrocarbon lubricant which is selected from the group consisting of di-n-long-chain alkaryls, linear mono-olefin oligomers, and a composition consisting essentially of di-n-long-chain alkaryls and trialkyl-substituted tetrahydronaphthalenes, wherein a. the term di-n-long-chain alkaryls refers to materials represented by the formula
6. The turbine oil composition of claim 5 wherein it contains from about 1 to about 15 weight percent tricresyl phosphate.
7. The turbine oil composition of claim 6 wherein (a) the amount of said copolymer is about 0.2 to about 0.6 weight percent, (b) the amount of said phosphite is about 0.5 to about 1.0 weight percent, and (c) the amount of said triazole is about 0.01 to about 0.04 weight percent.
8. The turbine oil composition of claim 5 wherein it contains from about 0.01 to about 0.15 weight percent of a partial ester of an alkyl or alkenyl succinic anhydride, which is represented by the formula:
9. A turbine oil composition comprising a major amount of a mineral or synthetic hydrocarbon base lubricating oil and the following combination of materials in tHe amounts specified, as weight percent of total composition: a. about 0.2 to about 0.6 - copolymer of about 1 mole of N-vinyl-2-pyrrolidone and about 1 mole of a C-20 Alpha -olefin; b. about 0.1 to about 1.0 - triphenyl phosphite or tri (mixed mono- and dinonylphenyl) phosphite; and c. about 0.01 to about 0.04 - benzotriazole or tolyltriazole.
10. The turbine oil composition of claim 9 wherein the base lubricating oil is a mineral oil.
11. The turbine oil composition of claim 10 wherein it contains from about 3 to about 8 weight percent tricresyl phosphate.
12. The turbine oil composition of claim 11 wherein it contains from about 0.04 to about 0.08 weight percent of a partial ester of succinic anhydride which is represented by the formula:
13. The turbine oil composition of claim 9 wherein the base lubricating oil is a synthetic hydrocarbon lubricant which is selected from the group consisting of di-n-long-chain alkaryls, linear mono-olefin oligomers, and a composition consisting essentially of di-n-long-chain alkaryls and trialkyl-substituted tetrahydronaphthalenes, wherein a. the term di-n-long-chain alkaryls refers to materials represented by the formula
14. The turbine oil compositions of claim 13 wherein it contains from about 3 to about 8 weight percent tricresyl phosphate.
15. The turbine oil composition of claim 14 wherein the base lubricating oil is a composition consisting essentially of di-n-long-chain alkaryls, which are present in an amount of 61 to 92 weight percent, and trialkyl-substituted tetrahydronaphthalenes which are present in an amount of 5 to 30 weight percent.
16. The turbine oil composition of claim 13 wherein it contains from about 0.04 to about 0.08 weight percent of a partial ester of succinic anhydride which is represented by the formula
17. The turbine oil composition of claim 16 wherein the base lubricating oil is a composition consisting essentially of di-n-long-chain alkaryls, which are present in an amount of 61 to 92 weight percent, and trialkyl-substituted tetrahydronaphthalenes which are present in an amount of 5 to 30 weight percent.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US512766A US3926823A (en) | 1974-10-07 | 1974-10-07 | Turbine oil compositions |
CA225,813A CA1051858A (en) | 1974-10-07 | 1975-04-24 | Turbine oil compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US512766A US3926823A (en) | 1974-10-07 | 1974-10-07 | Turbine oil compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
US3926823A true US3926823A (en) | 1975-12-16 |
Family
ID=24040466
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US512766A Expired - Lifetime US3926823A (en) | 1974-10-07 | 1974-10-07 | Turbine oil compositions |
Country Status (2)
Country | Link |
---|---|
US (1) | US3926823A (en) |
CA (1) | CA1051858A (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4146490A (en) * | 1977-12-02 | 1979-03-27 | Fmc Corporation | Turbine lubricant |
US4162225A (en) * | 1978-04-17 | 1979-07-24 | Mobil Oil Corporation | Lubricant compositions of enhanced antioxidant properties |
US4169800A (en) * | 1977-12-02 | 1979-10-02 | Fmc Corporation | Turbine lubricant |
US4170561A (en) * | 1974-12-12 | 1979-10-09 | Entreprise De Recherches Et D'activities Petrolieres (E.R.A.P.) | Lubricating compositions with lactam or thiolactam-containing copolymers |
US4171272A (en) * | 1977-12-02 | 1979-10-16 | Fmc Corporation | Turbine lubricant |
US4313840A (en) * | 1979-03-07 | 1982-02-02 | Agency Of Industrial Science And Technology | Heat transfer oil and method for driving a Freon turbine |
US4444649A (en) * | 1982-11-15 | 1984-04-24 | Union Oil Company Of California | Antifoulant for high temperature hydrocarbon processing |
US4461713A (en) * | 1983-04-01 | 1984-07-24 | Stauffer Chemical Company | Acid-resistant phosphate ester functional fluids |
US4466894A (en) * | 1983-04-20 | 1984-08-21 | The Lubrizol Corporation | Phosphorus-containing metal salts/sulfurized phenate compositions/aromatic substituted triazoles, concentrates, and functional fluids containing same |
US4626368A (en) * | 1985-12-10 | 1986-12-02 | Mobil Oil Corporation | Benzotriazole derivatives and organic compositions containing same |
US5080817A (en) * | 1990-09-18 | 1992-01-14 | Nalco Chemical Company | Corrosion inhibitor for 2-cycle engine oils comprising dodecenyl succinic anhydride-propylene glycol esters |
US6191078B1 (en) | 1999-09-21 | 2001-02-20 | Exxonmobil Research And Engineering Company | Part-synthetic, aviation piston engine lubricant |
US6207623B1 (en) | 2000-01-14 | 2001-03-27 | Exxonmobil Research And Engineering Company | Industrial oils of enhanced resistance to oxidation |
US6468946B2 (en) | 1998-07-06 | 2002-10-22 | The Lubrizol Corporation | Mixed phosphorus compounds and lubricants containing the same |
US20090186789A1 (en) * | 2006-05-15 | 2009-07-23 | Mitsuhiro Nagakari | Lubricating oil composition |
US9481841B2 (en) | 2004-12-09 | 2016-11-01 | The Lubrizol Corporation | Process of preparation of an additive and its use |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3778376A (en) * | 1966-07-05 | 1973-12-11 | Monsanto Co | Functional fluids |
US3790478A (en) * | 1971-04-30 | 1974-02-05 | British Petroleum Co | Synthetic lubricant for aero gas turbines |
US3790481A (en) * | 1971-04-30 | 1974-02-05 | British Petroleum Co | Synthetic lubricants for aero gas turbines |
-
1974
- 1974-10-07 US US512766A patent/US3926823A/en not_active Expired - Lifetime
-
1975
- 1975-04-24 CA CA225,813A patent/CA1051858A/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3778376A (en) * | 1966-07-05 | 1973-12-11 | Monsanto Co | Functional fluids |
US3790478A (en) * | 1971-04-30 | 1974-02-05 | British Petroleum Co | Synthetic lubricant for aero gas turbines |
US3790481A (en) * | 1971-04-30 | 1974-02-05 | British Petroleum Co | Synthetic lubricants for aero gas turbines |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4170561A (en) * | 1974-12-12 | 1979-10-09 | Entreprise De Recherches Et D'activities Petrolieres (E.R.A.P.) | Lubricating compositions with lactam or thiolactam-containing copolymers |
US4146490A (en) * | 1977-12-02 | 1979-03-27 | Fmc Corporation | Turbine lubricant |
US4169800A (en) * | 1977-12-02 | 1979-10-02 | Fmc Corporation | Turbine lubricant |
US4171272A (en) * | 1977-12-02 | 1979-10-16 | Fmc Corporation | Turbine lubricant |
US4162225A (en) * | 1978-04-17 | 1979-07-24 | Mobil Oil Corporation | Lubricant compositions of enhanced antioxidant properties |
US4313840A (en) * | 1979-03-07 | 1982-02-02 | Agency Of Industrial Science And Technology | Heat transfer oil and method for driving a Freon turbine |
US4444649A (en) * | 1982-11-15 | 1984-04-24 | Union Oil Company Of California | Antifoulant for high temperature hydrocarbon processing |
US4461713A (en) * | 1983-04-01 | 1984-07-24 | Stauffer Chemical Company | Acid-resistant phosphate ester functional fluids |
US4466894A (en) * | 1983-04-20 | 1984-08-21 | The Lubrizol Corporation | Phosphorus-containing metal salts/sulfurized phenate compositions/aromatic substituted triazoles, concentrates, and functional fluids containing same |
US4626368A (en) * | 1985-12-10 | 1986-12-02 | Mobil Oil Corporation | Benzotriazole derivatives and organic compositions containing same |
US5080817A (en) * | 1990-09-18 | 1992-01-14 | Nalco Chemical Company | Corrosion inhibitor for 2-cycle engine oils comprising dodecenyl succinic anhydride-propylene glycol esters |
US6468946B2 (en) | 1998-07-06 | 2002-10-22 | The Lubrizol Corporation | Mixed phosphorus compounds and lubricants containing the same |
US6191078B1 (en) | 1999-09-21 | 2001-02-20 | Exxonmobil Research And Engineering Company | Part-synthetic, aviation piston engine lubricant |
US6207623B1 (en) | 2000-01-14 | 2001-03-27 | Exxonmobil Research And Engineering Company | Industrial oils of enhanced resistance to oxidation |
US9481841B2 (en) | 2004-12-09 | 2016-11-01 | The Lubrizol Corporation | Process of preparation of an additive and its use |
US20090186789A1 (en) * | 2006-05-15 | 2009-07-23 | Mitsuhiro Nagakari | Lubricating oil composition |
Also Published As
Publication number | Publication date |
---|---|
CA1051858A (en) | 1979-04-03 |
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