WO2007045629A9 - Composition d’huile lubrifiante - Google Patents
Composition d’huile lubrifianteInfo
- Publication number
- WO2007045629A9 WO2007045629A9 PCT/EP2006/067444 EP2006067444W WO2007045629A9 WO 2007045629 A9 WO2007045629 A9 WO 2007045629A9 EP 2006067444 W EP2006067444 W EP 2006067444W WO 2007045629 A9 WO2007045629 A9 WO 2007045629A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- lubricating oil
- oil composition
- base oils
- phenyl
- composition according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 90
- 239000010687 lubricating oil Substances 0.000 title claims abstract description 67
- 239000002199 base oil Substances 0.000 claims abstract description 59
- 239000000314 lubricant Substances 0.000 claims abstract description 40
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 claims abstract description 26
- 125000003118 aryl group Chemical group 0.000 claims abstract description 21
- 229920013639 polyalphaolefin Polymers 0.000 claims abstract description 12
- 230000001050 lubricating effect Effects 0.000 claims abstract description 10
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 24
- 239000000654 additive Substances 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 7
- 239000007866 anti-wear additive Substances 0.000 claims description 6
- 150000002790 naphthalenes Chemical class 0.000 claims description 6
- 230000007797 corrosion Effects 0.000 claims description 4
- 238000005260 corrosion Methods 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000006260 foam Substances 0.000 claims description 3
- 239000005069 Extreme pressure additive Substances 0.000 claims description 2
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 125000006267 biphenyl group Chemical class 0.000 claims description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 2
- -1 diphenyl amines Chemical class 0.000 abstract description 11
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 14
- 239000003921 oil Substances 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- 239000003963 antioxidant agent Substances 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 5
- 229920001515 polyalkylene glycol Polymers 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical class C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- GLEAJEPGOSMZLQ-UHFFFAOYSA-N 1-octyl-n-(4-octylphenyl)naphthalen-2-amine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(C=CC=C2)C2=C1CCCCCCCC GLEAJEPGOSMZLQ-UHFFFAOYSA-N 0.000 description 1
- OIWIYLWZIIJNHU-UHFFFAOYSA-N 1-sulfanylpyrazole Chemical compound SN1C=CC=N1 OIWIYLWZIIJNHU-UHFFFAOYSA-N 0.000 description 1
- QVXGKJYMVLJYCL-UHFFFAOYSA-N 2,3-di(nonyl)-N-phenylaniline Chemical compound C(CCCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCCC QVXGKJYMVLJYCL-UHFFFAOYSA-N 0.000 description 1
- FCQAFXHLHBGGSK-UHFFFAOYSA-N 4-nonyl-n-(4-nonylphenyl)aniline Chemical compound C1=CC(CCCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCCC)C=C1 FCQAFXHLHBGGSK-UHFFFAOYSA-N 0.000 description 1
- UUNBFTCKFYBASS-UHFFFAOYSA-N C(CCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCC Chemical compound C(CCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCC UUNBFTCKFYBASS-UHFFFAOYSA-N 0.000 description 1
- 241000282461 Canis lupus Species 0.000 description 1
- QAPVYZRWKDXNDK-UHFFFAOYSA-N P,P-Dioctyldiphenylamine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCC)C=C1 QAPVYZRWKDXNDK-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XYRMLECORMNZEY-UHFFFAOYSA-B [Mo+4].[Mo+4].[Mo+4].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S Chemical compound [Mo+4].[Mo+4].[Mo+4].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S XYRMLECORMNZEY-UHFFFAOYSA-B 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000005078 molybdenum compound Substances 0.000 description 1
- 150000002752 molybdenum compounds Chemical class 0.000 description 1
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical class C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 1
- JSIRUVGNQVWPSE-UHFFFAOYSA-N n-(2-dodecylphenyl)naphthalen-1-amine Chemical compound CCCCCCCCCCCCC1=CC=CC=C1NC1=CC=CC2=CC=CC=C12 JSIRUVGNQVWPSE-UHFFFAOYSA-N 0.000 description 1
- XEJIYLJRGKVDPF-UHFFFAOYSA-N n-(4-dodecylphenyl)naphthalen-1-amine Chemical compound C1=CC(CCCCCCCCCCCC)=CC=C1NC1=CC=CC2=CC=CC=C12 XEJIYLJRGKVDPF-UHFFFAOYSA-N 0.000 description 1
- BQLZCNHPJNMDIO-UHFFFAOYSA-N n-(4-octylphenyl)naphthalen-1-amine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=CC2=CC=CC=C12 BQLZCNHPJNMDIO-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- SRWPBFLLYKIZTL-UHFFFAOYSA-N n-hexyl-n-phenylnaphthalen-2-amine Chemical compound C=1C=C2C=CC=CC2=CC=1N(CCCCCC)C1=CC=CC=C1 SRWPBFLLYKIZTL-UHFFFAOYSA-N 0.000 description 1
- RQVGZVZFVNMBGS-UHFFFAOYSA-N n-octyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(CCCCCCCC)C1=CC=CC=C1 RQVGZVZFVNMBGS-UHFFFAOYSA-N 0.000 description 1
- SNWVRVDHQRBBFG-UHFFFAOYSA-N n-phenyl-n-(2,4,4-trimethylpentan-2-yl)naphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(C(C)(C)CC(C)(C)C)C1=CC=CC=C1 SNWVRVDHQRBBFG-UHFFFAOYSA-N 0.000 description 1
- MHJCZOMOUCUAOI-UHFFFAOYSA-N n-tert-butyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(C(C)(C)C)C1=CC=CC=C1 MHJCZOMOUCUAOI-UHFFFAOYSA-N 0.000 description 1
- 230000036542 oxidative stress Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/12—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
- C10M2203/065—Well-defined aromatic compounds used as base material
-
- 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
- C10M2203/104—Aromatic fractions
- C10M2203/1045—Aromatic fractions used as base material
-
- 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
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
- C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
-
- 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
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
-
- 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
- C10M2205/22—Alkylation reaction products with aromatic type compounds, e.g. Friedel-crafts
- C10M2205/223—Alkylation reaction products with aromatic type compounds, e.g. Friedel-crafts used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
-
- 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
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
-
- 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
- C10N2040/30—Refrigerators lubricants or compressors lubricants
Definitions
- the present invention relates to lubricating compositions, more specifically to lubricating compositions for lubricating rotary air compressors.
- the lubrication of compressors in particular rotary air compressors, can expose the lubricant to high temperature conditions .
- Lubricating oil compositions for use in such compressors have to meet a combination of requirements in order to satisfactorily lubricate each component. Accordingly, in order that the need for oil changes can be minimised in such compressors, i.e. in order that the oil drain interval is favourable, such lubricating oil compositions must exhibit not only good deposit control, but also good thermal and oxidative stability.
- WO-A-01/64820 describes a lubricating oil composition comprising a lubricating basestock which comprises a blend of (A) at least one polyalkylene glycol (PAG) and (B) at least one alkyl aromatic compound.
- said lubricating oil composition can be used as a positive displacement compressor lubricant.
- WO-A-01/64820 exemplifies lubricating oil compositions comprising a PAG in combination with an alkyl naphthalene and various antioxidants .
- EP-A-0387979 discloses specific alkyl-substituted diphenylamines as antioxidants, i.e. p,p'- dinonyldiphenylamines .
- EP-A-0387979 further discloses the use of said antioxidants in lubricating oil compositions comprising mineral oil having an aromatic content of 30% by weight or below and/or synthetic oil containing no aromatic rings in its structural units . That is to say, EP-A-0387979 teaches away from the use of said antioxidants with aromatic lubricant base oils .
- EP-A-0387979 discloses a composition comprising a p, p' -dinonyldiphenylamine, N-p-dodecylphenyl- ⁇ - naphthylamine, and, as base oil, either a purified mineral oil having an aromatic content of 7% by weight or a poly- oc-olefin oil.
- base oil either a purified mineral oil having an aromatic content of 7% by weight or a poly- oc-olefin oil.
- Table 2 of EP-A-0387979 discloses a composition comprising p, p' -branched dinonyldiphenylamine (Ex. 5) and N-p-branched dodecylphenyl- ⁇ -naphthylamine in said purified mineral oil which has an oxidation-inhibiting performance (according to ASTM D2272) of 2154 minutes.
- Comparative Example 4 in said Table describes a composition comprising p, p' -branched dioctyldiphenylamine and N-p-branched octylphenyl-OC- naphthylamine in said purified mineral oil which has an oxidation-inhibiting performance (according to ASTM D2272) of 2127 minutes.
- US-B1-6180575 describes lubricating oil compositions which may be used in the lubrication of bearings, gears and in other industrial applications such as in wet clutch systems, cooling gear boxes and rotary screw compressors .
- Said lubricating oil compositions comprise a base fluid which comprises at least 50 wt . % of a hydrocarbon base fluid; and an additive combination comprising: (1) an adduct of a substituted triazole and a hydrocarbon amine phosphate in an amount below about 5 wt . % of the total composition and (2) a tri-hydrocarbyl phosphate in an amount up to
- US-B1-6180575 lists an number of conventional additives including viscosity index improvers, antioxidants, anti-wear additives and corrosion inhibitors which may also be present in said lubricating oil compositions. It is of note that whilst US-Bl- 6180575 lists a number of different kinds of antioxidants in the description thereof, the antioxidants are not a critical feature of the Examples in US-B1-6180575 and they are not described in detail therein.
- Example 3 of US-B1-6180575 is said to be an ISO grade 32 oil comprising 20.00 %wt . C14 alkyl naphthalene, 76.78 %wt . of a mixture of PAO and 0.75 %wt . of an amine antioxidant. Said oil is indicated to have a RBOT value of 1750 minutes according to ASTM D2272.
- lubricating oil compositions have been surprisingly found which not only exhibit good deposit control, but which also exhibit excellent oxidative and thermal stability.
- the lubricating oil composition according to the present invention comprises one or more hydrocarbyl- substituted aromatic lubricant base oils in combination with (a) one or more phenyl-naphthylamines and (b) one or more diphenylamines, wherein said lubricating oil composition comprises one or more additional lubricant base oils comprising polyalphaolefins and/or Fischer- Tropsch derived base oils .
- the lubricating composition according to the present invention can comprise a single compound or a mixture of compounds for each of components (a) and (b) .
- the one or more phenyl-naphthylamines (a) which are used in the present invention, can be either substituted or non-substituted, or a mixture of both.
- the one or more phenyl-naphthylamines can be used as such or in the form of a salt. Examples of such phenyl-naphthylamines are phenyl-alpha-naphthylamines and phenyl-beta- naphthylamines .
- the phenyl-naphthylamine preferably is a phenyl-alpha-naphthylamine .
- a preferred substituted phenyl-naphthylamine is a mono-alkylated phenyl-alpha-naphthylamine.
- phenyl-naphthylamines examples include octylphenyl-beta-naphthylamine, t-octylphenyl-alpha-naphthylamine, phenyl-alpha- naphthylamine, phenyl-beta-naphthylamine, phenyl-beta- naphthylamine, p-octylphenyl-alpha-naphthylamine, 4-octylphenyl-l-octyl-beta-naphthylamine, n-t-dodecylphenyl-1-naphthylamine, N-hexylphenyl-2- naphthylamine .
- a particularly preferred phenyl-alpha- naphthylamine is a monooctylated phenyl alpha- naphthylamine,
- Another preferred phenyl-naphthylamine is a non- substituted phenyl-alpha-naphthylamine .
- phenyl- naphthylamines that may be conveniently used in the lubricating oil composition of the present invention include that available from Ciba Specialty Chemicals under the trade designation "IRGANOX L-06".
- the lubricating oil composition according to the present invention further comprises one or more diphenylamines (b) .
- the one or more diphenylamines can be substituted or non-substituted. It is preferred to use a hydrocarbyl-substituted diphenylamine, more preferably an alkyl-substituted diphenylamine.
- a preferred diphenylamine is 4,4'-dialkyl diphenylamine.
- the alkyl group preferably contains in the range of from 2 to 15 carbon atoms, more preferably in the range of from 3 to 12 carbon atoms.
- Preferred diphenylamines include dialkyldiphenylamines such as p, p ' -dioctyl-diphenylamine, p, p ' -di- ⁇ -methylbenzyl-diphenylamine and N-p-butylphenyl- N-p ' -octylphenylamine, monoalkyldiphenylamines such as mono-t-butyldiphenylamine and mono-octyldiphenylamine, bis (dialkylphenyl) amines such as di-(2,4- diethylphenyl) amine and di (2-ethyl-4-nonylphenyl) amine .
- dialkyldiphenylamines such as p, p ' -dioctyl-diphenylamine, p, p ' -di- ⁇ -methylbenzyl-diphenylamine and N-p-butyl
- the one or more hydrocarbyl-substituted aromatic lubricant base oils present in the lubricating oil composition of the present invention are preferably alkylated aromatic lubricant base oils, more preferably alkylated aromatic lubricant base oils selected from one or more of alkylated naphthalenes, alkylated benzenes, alkylated diphenyl compounds and alkylated diphenyl methanes.
- Such base oils are described in US-B1-6180575 and may be conveniently prepared by the methods described therein.
- the one or more hydrocarbyl- substituted aromatic lubricant base oils essentially consist of compounds which only contain hydrogen and carbon. A limited amount of contaminants such as sulphur containing compounds may be present therein.
- more than 80 %wt of the one or more hydrocarbyl- substituted aromatic lubricant base oils consists of compounds consisting of hydrogen and carbon only, more preferably more than 90 %wt .
- Alkylated naphthalenes are preferred hydrocarbyl- substituted aromatic lubricant base oils for use in the lubricating oil compositions of the present invention.
- Said alkylated naphthalenes may be mono-, di-, tri or tetra-alkyl substituted naphthalenes such as those desscribed in US-A-5602086, WO-A-03/048275 and WO-A-03/048276.
- the lubricating oil composition of the present invention comprises one or more additional lubricant base oils comprising polyalphaolefins and/or Fischer-Tropsch derived base oils .
- polyalphaolefins and their manufacture are well known in the art.
- Preferred polyalphaolefins that may be used in lubricating oil compositions of the present invention may be derived from C2 to C32 alpha olefins.
- Particularly preferred feedstocks for said polyalphaolefins are 1- octene, 1-decene, 1-dodecene and 1-tetradecene .
- polyalphaolefins that may be conveniently used in the lubricating oil compositions of the present invention have a kinematic viscosity at 100 0 C in the range of from 3 to 300 mm 2 /s, more preferably in the range of from 4 to 100 mm ⁇ /s.
- Fischer-Tropsch derived base oils which may be conveniently used as the one or more additional base oils in the lubricating oil composition of the present invention include, for example, the Fischer-Tropsch derived base oils disclosed in EP-A-776959, EP-A-668342, WO-A-97/21788, WO-A-00/15736, WO-A-00/14188, WO-A- 00/14187, WO-A-00/14183, WO-A-00/14179, WO-A-00/08115, WO-A-99/41332, EP-A-1029029, WO-A-01/18156 and WO-A- 01/57166.
- said one or more additional lubricant base oils may further comprise mineral and/or other synthetic lubricant base oils .
- Such mineral lubricant base oils include liquid petroleum oils and solvent treated or acid treated mineral lubricating oils of the paraffinic, naphthenic, or mixed paraffinic/naphthenic type which may be further refined by hydrocracking and hydrofinishing processes and/or dewaxing.
- Naphthenic base oils have low viscosity index (VI) (generally 40-80) and a low pour point. Such base oils are produced from feedstocks rich in naphthenes and low in wax content and are used mainly for lubricants in which colour and colour stability are important, and VI and oxidation stability are of secondary importance. Paraffinic base oils have higher VI (generally >95) and a high pour point. Said base oils are produced from feedstocks rich in paraffins, and are used for lubricants in which VI and oxidation stability are important.
- VI viscosity index
- Synthetic processes enable molecules to be built from simpler substances or to have their structures modified to give the precise properties required.
- Other synthetic lubricant base oils which may be present in the one or more additional lubricant base oils include hydrocarbon oils such as polyalkylene glycols (PAGs), polyisobutylenes (PIBs) dibasic acids esters, polyol esters and other complex esters, and dewaxed waxy raffinate. Synthetic hydrocarbon base oils sold by the Shell Group under the designation "XHVI” (trade mark) may be conveniently used.
- Optional additional lubricant base oils are preferably constituted from mineral oils and/or other synthetic base oils which contain more than 80% wt of saturates, more preferably more than 90 % wt., as measured according to ASTM D2007.
- said optional additional lubricant base oils contain less than 1.0 wt . %, more preferably less than 0.1 wt . % of sulphur, calculated as elemental sulphur and measured according to ASTM D2622, ASTM D4294, ASTM D4927 or ASTM D3120.
- the viscosity index of said optional additional lubricant base oils is more than 80, more preferably more than 120, as measured according to ASTM D2270.
- the lubricating oil composition of the present invention has a kinematic viscosity in the range of from 32 to 150 mm ⁇ /s at 40 0 C, more preferably in the range of from 32 to 100 mm ⁇ /s, and most preferably in the range of from 32 to 78 mm ⁇ /s.
- the amount of the additives (a) and (b) present in the lubricating oil composition of the present invention depends on the specific compounds used therein.
- the lubricating oil composition of the present invention preferably comprises a total amount in the range of from 0.1 to 5.0 % by weight, more preferably in the range of from 0.2 to 2.0 % by weight of said one or more phenyl-naphthylamines, based on the total weight of the lubricating oil composition.
- the lubricating oil composition of the present invention preferably comprises a total amount in the range of from 0.1 to 5.0 % by weight, more preferably in the range of from 0.2 to 2.0 % by weight, of said one or more diphenylamines, based on total weight of the lubricating oil composition.
- hydrocarbyl-substituted aromatic lubricant base oils are preferably present in the lubricating oil composition of the present invention in a total amount in the range of from 0.1 to 30 % by weight, more preferably in the range of from 1 to 20 % by weight, based on the total weight of the lubricating oil composition.
- the one or more hydrocarbyl-substituted aromatic lubricant base oils preferably comprise less than 60 wt. % of the total lubricant base oil in the lubricating oil composition of the present invention, more preferably less than 25 wt . % of the total lubricant base oil and most preferably in the range of from 1 to 25 wt .% of the total weight of lubricant base oil, wherein the total weight of lubricant base oil is the total weight of the one or more hydrocarbyl-substituted aromatic lubricant base oils and the one or more additional lubricant base oils .
- the one or more phenyl-naphthylamines (a) and the one or more diphenylamines (b) are present in the lubricating oil composition of the present invention in a weight ratio in the range of from 1:3 to 3:1, more preferably in the range of from 1:2 to 1:1. It is preferred that the lubricating oil composition according to the present invention contains no substantial amount of phenolic antioxidant .
- the amount of phenolic antioxidant present preferably is less than 1 % by weight, more preferably less than 0.5 % by weight, even more preferably less than 0.1 % by weight, and most preferably 0 % by weight, based on total amount of the lubricating oil composition.
- the lubricating oil composition of the present invention can further comprise additives such as extreme pressure additives, anti-wear additives, metal passivators, corrosion inhibitors, foam inhibitors and/or demulsifiers .
- Anti-wear additives that may be conveniently used include zinc dithiophosphate compounds selected from zinc dialkyl-, diaryl- and/or alkylaryl- dithiophosphates, molybdenum-containing compounds, boron-containing compounds and ashless anti-wear additives such as substituted or unsubstituted thiophosphoric acids, and salts thereof.
- Said anti-wear additives may each be conveniently added to the lubricating oil composition of the present invention in an amount in the range of from 0.1 to 3.0 wt. %, based on the total weight of lubricating oil composition.
- molybdenum-containing compounds may conveniently include molybdenum dithiocarbamates, trinuclear molybdenum compounds, for example as described in WO-A-98/26030, sulphides of molybdenum and molybdenum dithiophosphate .
- Boron-containing compounds that may be conveniently used include borate esters, borated fatty amines, borated epoxides, alkali metal (or mixed alkali metal or alkaline earth metal) borates and borated overbased metal salts.
- Compounds such as alkenyl succinic acid or ester moieties thereof, benzotriazole-based compounds and thiodiazole-based compounds may be conveniently used in the lubricating oil composition of the present invention as corrosion inhibitors.
- Compounds such as polysiloxanes, dimethyl polycyclohexane and polyacrylates may be conveniently used in the lubricating oil composition of the present invention as foam inhibitors.
- the present invention further provides the use of the lubricating oil composition according to the present invention for lubricating a rotary air compressor.
- the lubricating composition according to the present invention can be conveniently prepared by blending together the one or more phenyl-naphthylamines, the one or more diphenylamines, the one or more hydrocarbyl- substituted aromatic lubricant base oils and the one or more additional lubricant base oils comprising polyalphaolefins and/or Fischer-Tropsch derived base oils and, optionally, one or more additives as hereinbefore described.
- phenyl-naphthylamine (a) used in the formulations of Tables 1 and 2 was that available from Ciba Specialty Chemicals under the trade designations "IRGANOX L-06".
- the diphenylamine (b) used in the formulations of Tables 1 and 2 was that available from Ciba Specialty Chemicals under the trade designation "IRGANOX L-57”.
- the hydrocarbyl-substituted aromatic lubricant base oil used in the formulations of Tables 1 and 2 was the alkyl naphthalene available under the trade designation "SYNESSTIC 5" from ExxonMobil.
- the PAO 40 base oil used in the formulations of Tables 1 and 2 was that available from Innovene under the trade designation "DURASYN 174".
- PAO 8 base oil used in the formulations of Table 1 was that available from Innovene under the trade designation "DURASYN 168".
- the GTL 8 base oil used in the formulations of Table 2 was a Fischer-Tropsch derived base oil having a kinematic viscosity at 100 0 C of approx. 8 cSt (IHm 2 S "1 ) .
- Said base oil may be conveniently manufactured by the process described in WO-A-02/070631.
- Examples 1 and 2 are according to the present invention whilst the remaining Examples in Tables 1 and 2 are comparative in nature .
- the formulations in Tables 1 and 2 were subjected to the Rotating Pressure Vessel Oxidation Test (RPVOT) (formerly known as the Rotating Bomb Oxidation Test (RBOT)) (ASTM D2272) in order to measure the oxidative stability thereof.
- RVOT Rotating Pressure Vessel Oxidation Test
- RBOT Rotating Bomb Oxidation Test
- ASTM D2272 Standard D2272
- said formulations were also tested in a version of the Wolf Strip Test (formerly known as DIN 51392) performed according to the modifications set out below.
- DIN 51392 formerly measured the tendency of engine oils to produce thermal/oxidative deposits using an inclined metal plate over which the test engine oils were pumped.
- the volume of oil, pumping rate, plate temperature and test duration specified in said test were
- test conditions used in the Examples of Tables 1 and 2 were modified to an oil volume of 150 ml, a pumping rate of 50 ml/hour, a plate temperature of 205 0 C and a test duration of 24 hours. It is apparent from Tables 1 and 2 that the formulations in accordance with the present invention not only exhibit good deposit control but also display outstanding performance in the RPVOT.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Priority Applications (5)
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JP2008536036A JP2009511728A (ja) | 2005-10-17 | 2006-10-16 | 潤滑油組成物 |
AU2006303337A AU2006303337A1 (en) | 2005-10-17 | 2006-10-16 | Lubricating oil composition |
BRPI0617445-0A BRPI0617445A2 (pt) | 2005-10-17 | 2006-10-16 | composiÇço de àleo lubrificante, e, uso da mesma |
CA002626036A CA2626036A1 (fr) | 2005-10-17 | 2006-10-16 | Composition d'huile lubrifiante |
EP06807300A EP1937792A1 (fr) | 2005-10-17 | 2006-10-16 | Composition d huile lubrifiante |
Applications Claiming Priority (2)
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EP05256430 | 2005-10-17 | ||
EP05256430.9 | 2005-10-17 |
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WO2007045629A1 WO2007045629A1 (fr) | 2007-04-26 |
WO2007045629A9 true WO2007045629A9 (fr) | 2008-07-03 |
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PCT/EP2006/067444 WO2007045629A1 (fr) | 2005-10-17 | 2006-10-16 | Composition d’huile lubrifiante |
Country Status (10)
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US (1) | US20070129268A1 (fr) |
EP (1) | EP1937792A1 (fr) |
JP (1) | JP2009511728A (fr) |
KR (1) | KR20080056019A (fr) |
CN (1) | CN101310004A (fr) |
AU (1) | AU2006303337A1 (fr) |
BR (1) | BRPI0617445A2 (fr) |
CA (1) | CA2626036A1 (fr) |
WO (1) | WO2007045629A1 (fr) |
ZA (1) | ZA200803157B (fr) |
Families Citing this family (22)
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US20090181871A1 (en) * | 2007-12-19 | 2009-07-16 | Chevron U.S.A. Inc. | Compressor Lubricant Compositions and Preparation Thereof |
US8187455B2 (en) * | 2008-07-18 | 2012-05-29 | Socomer Nv. | Voltammetric technique to determine the individual concentration of different antioxidants of the same class |
US8227391B2 (en) † | 2008-10-17 | 2012-07-24 | Afton Chemical Corporation | Lubricating composition with good oxidative stability and reduced deposit formation |
WO2010149706A1 (fr) | 2009-06-24 | 2010-12-29 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
US8716201B2 (en) | 2009-10-02 | 2014-05-06 | Exxonmobil Research And Engineering Company | Alkylated naphtylene base stock lubricant formulations |
KR101722380B1 (ko) * | 2009-10-09 | 2017-04-05 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 윤활 조성물 |
EP2192168A1 (fr) * | 2009-11-25 | 2010-06-02 | Shell Internationale Research Maatschappij B.V. | Concentré d'additifs |
US9150812B2 (en) | 2012-03-22 | 2015-10-06 | Exxonmobil Research And Engineering Company | Antioxidant combination and synthetic base oils containing the same |
WO2013146805A1 (fr) * | 2012-03-29 | 2013-10-03 | 出光興産株式会社 | Composition d'huile lubrifiante pour des compresseurs d'air |
BR112014031498A2 (pt) | 2012-06-21 | 2017-06-27 | Shell Int Research | composição lubrificante, e, uso de uma composição lubrificante |
EP2816097A1 (fr) | 2013-06-18 | 2014-12-24 | Shell Internationale Research Maatschappij B.V. | Composition d'huile de lubrification |
EP2816098A1 (fr) | 2013-06-18 | 2014-12-24 | Shell Internationale Research Maatschappij B.V. | Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification |
JP6829601B2 (ja) | 2013-12-24 | 2021-02-10 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイShell Internationale Research Maatschappij Besloten Vennootshap | 潤滑組成物 |
WO2016043800A1 (fr) * | 2014-09-19 | 2016-03-24 | Vanderbilt Chemicals, Llc | Compositions de lubrifiant industriel à base de polyalkylèneglycol |
US10160927B2 (en) | 2014-12-17 | 2018-12-25 | Shell Oil Company | Lubricating oil composition |
US11162048B2 (en) * | 2016-12-27 | 2021-11-02 | The Lubrizol Corporation | Lubricating composition with alkylated naphthylamine |
US20180305633A1 (en) | 2017-04-19 | 2018-10-25 | Shell Oil Company | Lubricating compositions comprising a volatility reducing additive |
WO2020190859A1 (fr) * | 2019-03-20 | 2020-09-24 | Basf Se | Composition lubrifiante |
CN110079375B (zh) * | 2019-04-15 | 2022-10-18 | 北京雅士科莱恩石油化工有限公司 | 一种螺杆压缩机油及其制备方法 |
US11976251B2 (en) * | 2019-12-18 | 2024-05-07 | ExxonMobil Technology and Engineering Company | Method for controlling lubrication of a rotary shaft seal |
CN111575082B (zh) * | 2020-06-16 | 2021-09-07 | 烟台德高石油有限公司 | 一种新能源车载滑片式空气压缩机用压缩机油及其制备方法 |
CN111575084B (zh) * | 2020-06-16 | 2021-10-26 | 烟台德高石油有限公司 | 一种合成抗水型长寿命真空泵油及其制备方法 |
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JPS62124193A (ja) * | 1985-11-25 | 1987-06-05 | Nishi Nippon Tsusho Kk | 冷凍機油組成物 |
JPH01115998A (ja) * | 1987-10-28 | 1989-05-09 | Idemitsu Kosan Co Ltd | 水素含有フロン冷媒用潤滑油及び組成物 |
JP2539677B2 (ja) * | 1989-01-13 | 1996-10-02 | 日本石油株式会社 | 潤滑油組成物 |
JP2587296B2 (ja) * | 1989-09-08 | 1997-03-05 | 日本石油株式会社 | 潤滑油組成物 |
ES2051608T3 (es) * | 1991-01-11 | 1994-06-16 | Mobil Oil Corp | Composiciones lubricantes. |
US5236610A (en) * | 1992-02-03 | 1993-08-17 | The United States Of America As Represented By The Secretary Of The Commerce | Stable high temperature liquid lubricant blends and antioxidant additives for use therewith |
JP3261978B2 (ja) * | 1996-06-03 | 2002-03-04 | 出光興産株式会社 | ウオームギヤ油組成物 |
US6090989A (en) | 1997-10-20 | 2000-07-18 | Mobil Oil Corporation | Isoparaffinic lube basestock compositions |
US6059955A (en) | 1998-02-13 | 2000-05-09 | Exxon Research And Engineering Co. | Low viscosity lube basestock |
US6180575B1 (en) * | 1998-08-04 | 2001-01-30 | Mobil Oil Corporation | High performance lubricating oils |
US6008164A (en) | 1998-08-04 | 1999-12-28 | Exxon Research And Engineering Company | Lubricant base oil having improved oxidative stability |
US6103099A (en) | 1998-09-04 | 2000-08-15 | Exxon Research And Engineering Company | Production of synthetic lubricant and lubricant base stock without dewaxing |
US6475960B1 (en) | 1998-09-04 | 2002-11-05 | Exxonmobil Research And Engineering Co. | Premium synthetic lubricants |
US6080301A (en) | 1998-09-04 | 2000-06-27 | Exxonmobil Research And Engineering Company | Premium synthetic lubricant base stock having at least 95% non-cyclic isoparaffins |
WO2001064820A1 (fr) * | 1999-02-19 | 2001-09-07 | The Lubrizol Corporation | Composition lubrifiante renfermant un melange d'un polyalkylene glycol et d'un alkyle aromatique et procede de lubrification |
FR2798136B1 (fr) | 1999-09-08 | 2001-11-16 | Total Raffinage Distribution | Nouvelle huile de base hydrocarbonee pour lubrifiants a indice de viscosite tres eleve |
US7067049B1 (en) | 2000-02-04 | 2006-06-27 | Exxonmobil Oil Corporation | Formulated lubricant oils containing high-performance base oils derived from highly paraffinic hydrocarbons |
JP4772284B2 (ja) * | 2004-01-08 | 2011-09-14 | Jx日鉱日石エネルギー株式会社 | 潤滑油組成物 |
-
2006
- 2006-10-16 WO PCT/EP2006/067444 patent/WO2007045629A1/fr active Application Filing
- 2006-10-16 KR KR1020087011672A patent/KR20080056019A/ko not_active Ceased
- 2006-10-16 CN CNA2006800423705A patent/CN101310004A/zh active Pending
- 2006-10-16 EP EP06807300A patent/EP1937792A1/fr not_active Withdrawn
- 2006-10-16 CA CA002626036A patent/CA2626036A1/fr not_active Abandoned
- 2006-10-16 JP JP2008536036A patent/JP2009511728A/ja active Pending
- 2006-10-16 AU AU2006303337A patent/AU2006303337A1/en not_active Abandoned
- 2006-10-16 BR BRPI0617445-0A patent/BRPI0617445A2/pt not_active IP Right Cessation
- 2006-10-17 US US11/582,457 patent/US20070129268A1/en not_active Abandoned
-
2008
- 2008-04-10 ZA ZA200803157A patent/ZA200803157B/xx unknown
Also Published As
Publication number | Publication date |
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AU2006303337A1 (en) | 2007-04-26 |
CN101310004A (zh) | 2008-11-19 |
EP1937792A1 (fr) | 2008-07-02 |
JP2009511728A (ja) | 2009-03-19 |
KR20080056019A (ko) | 2008-06-19 |
US20070129268A1 (en) | 2007-06-07 |
BRPI0617445A2 (pt) | 2011-07-26 |
ZA200803157B (en) | 2009-06-24 |
WO2007045629A1 (fr) | 2007-04-26 |
CA2626036A1 (fr) | 2007-04-26 |
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