EP1844128B1 - Verfahren zur regulierung der viskosität - Google Patents
Verfahren zur regulierung der viskosität Download PDFInfo
- Publication number
- EP1844128B1 EP1844128B1 EP05853765.5A EP05853765A EP1844128B1 EP 1844128 B1 EP1844128 B1 EP 1844128B1 EP 05853765 A EP05853765 A EP 05853765A EP 1844128 B1 EP1844128 B1 EP 1844128B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- viscosity
- viscosity modifier
- lubricating composition
- crankcase
- lubricating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 238000000034 method Methods 0.000 title claims description 25
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- 238000002485 combustion reaction Methods 0.000 claims description 20
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 14
- 239000000178 monomer Substances 0.000 claims description 14
- 229910052698 phosphorus Inorganic materials 0.000 claims description 14
- 239000011574 phosphorus Substances 0.000 claims description 14
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
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- 239000000654 additive Substances 0.000 description 12
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
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- PTYXPKUPXPWHSH-UHFFFAOYSA-N 1-(butyltetrasulfanyl)butane Chemical compound CCCCSSSSCCCC PTYXPKUPXPWHSH-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
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- 101100219315 Arabidopsis thaliana CYP83A1 gene Proteins 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
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- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 238000005698 Diels-Alder reaction Methods 0.000 description 2
- 101000806846 Homo sapiens DNA-(apurinic or apyrimidinic site) endonuclease Proteins 0.000 description 2
- 101000835083 Homo sapiens Tissue factor pathway inhibitor 2 Proteins 0.000 description 2
- 101100269674 Mus musculus Alyref2 gene Proteins 0.000 description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 101100140580 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) REF2 gene Proteins 0.000 description 2
- 102100026134 Tissue factor pathway inhibitor 2 Human genes 0.000 description 2
- CIBXCRZMRTUUFI-UHFFFAOYSA-N [chloro-[[chloro(phenyl)methyl]disulfanyl]methyl]benzene Chemical compound C=1C=CC=CC=1C(Cl)SSC(Cl)C1=CC=CC=C1 CIBXCRZMRTUUFI-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000007866 anti-wear additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000006078 metal deactivator Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- 150000000178 1,2,4-triazoles Chemical class 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- QDCPNGVVOWVKJG-VAWYXSNFSA-N 2-[(e)-dodec-1-enyl]butanedioic acid Chemical compound CCCCCCCCCC\C=C\C(C(O)=O)CC(O)=O QDCPNGVVOWVKJG-VAWYXSNFSA-N 0.000 description 1
- GASMGDMKGYYAHY-UHFFFAOYSA-N 2-methylidenehexanamide Chemical group CCCCC(=C)C(N)=O GASMGDMKGYYAHY-UHFFFAOYSA-N 0.000 description 1
- LNMBCRKRCIMQLW-UHFFFAOYSA-N 2-tert-butylsulfanyl-2-methylpropane Chemical compound CC(C)(C)SC(C)(C)C LNMBCRKRCIMQLW-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- WVRNUXJQQFPNMN-VAWYXSNFSA-N 3-[(e)-dodec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCC\C=C\C1CC(=O)OC1=O WVRNUXJQQFPNMN-VAWYXSNFSA-N 0.000 description 1
- ZWAPMFBHEQZLGK-UHFFFAOYSA-N 5-(dimethylamino)-2-methylidenepentanamide Chemical compound CN(C)CCCC(=C)C(N)=O ZWAPMFBHEQZLGK-UHFFFAOYSA-N 0.000 description 1
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 description 1
- FKIWNQVAKIZRMW-UHFFFAOYSA-N 6-(dimethylamino)-2-methylidenehexanamide;n-methylmethanamine;propyl 2-methylprop-2-enoate Chemical compound CNC.CCCOC(=O)C(C)=C.CN(C)CCCCC(=C)C(N)=O FKIWNQVAKIZRMW-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- HJRYTDKISXDCLR-UHFFFAOYSA-N C(CCCCCC)C1=C(C=CC=C1)O.[Ba] Chemical compound C(CCCCCC)C1=C(C=CC=C1)O.[Ba] HJRYTDKISXDCLR-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- GLOYGJPNNKTDIG-UHFFFAOYSA-N SC=1N=NSC=1S Chemical class SC=1N=NSC=1S GLOYGJPNNKTDIG-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical compound 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
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- RCLLINSDAJVOHP-UHFFFAOYSA-N n-ethyl-n',n'-dimethylprop-2-enehydrazide Chemical compound CCN(N(C)C)C(=O)C=C RCLLINSDAJVOHP-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- LQNPIBHEOATAEO-UHFFFAOYSA-N octanoate;octylazanium Chemical compound CCCCCCCCN.CCCCCCCC(O)=O LQNPIBHEOATAEO-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical compound OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229910052723 transition metal Chemical class 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- USEBTXRETYRZKO-UHFFFAOYSA-L zinc;n,n-dioctylcarbamodithioate Chemical compound [Zn+2].CCCCCCCCN(C([S-])=S)CCCCCCCC.CCCCCCCCN(C([S-])=S)CCCCCCCC USEBTXRETYRZKO-UHFFFAOYSA-L 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
- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
-
- 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
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
- C10M145/12—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate monocarboxylic
- C10M145/14—Acrylate; Methacrylate
-
- 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
- C10M161/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
-
- 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
- C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular 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
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
-
- 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
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/02—Viscosity; Viscosity index
-
- 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
- C10N2030/02—Pour-point; Viscosity index
-
- 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
- C10N2030/40—Low content or no content compositions
- C10N2030/42—Phosphor free or low phosphor content compositions
-
- 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
- C10N2030/68—Shear stability
-
- 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
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- 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
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01M—LUBRICATING OF MACHINES OR ENGINES IN GENERAL; LUBRICATING INTERNAL COMBUSTION ENGINES; CRANKCASE VENTILATING
- F01M9/00—Lubrication means having pertinent characteristics not provided for in, or of interest apart from, groups F01M1/00 - F01M7/00
- F01M9/02—Lubrication means having pertinent characteristics not provided for in, or of interest apart from, groups F01M1/00 - F01M7/00 having means for introducing additives to lubricant
Definitions
- lubricating oils It is well known for lubricating oils to contain a number of additives used to protect the engine from wear and provide viscosity control.
- Common additives for engine lubricating oils include zinc dialkyldithiophosphate (ZDDP) an antiwear additive. It is believed that ZDDP antiwear additives protect the engine by forming a protective film on metal surfaces.
- ZDDP antiwear additives protect the engine by forming a protective film on metal surfaces.
- Viscosity modifiers with a number average molecular weight above 100,000 are known in crankcase applications as viscosity modifiers because they help control high temperature viscometrics in multi-grade lubricants. Viscosity modifiers in various applications are known from, e.g., U.S. Patent 5,112,509 .
- any reduction in the performance of catalytic converters caused by phosphorus poisoning tends to result in increased amounts of greenhouse gases such as nitric oxide and/or ash formation.
- reducing the amount of ZDDP will increase the amount of wear in an engine crankcase.
- This invention provides a method of lubricating an internal combustion engine comprising a crankcase and at least one of a gear and a wet-clutch, said method comprising supplying to said crankcase and to at least one of the gear and wet-clutch a lubricating composition comprising: (a) an oil of lubricating viscosity; and (b) a viscosity modifier with a number average molecular weight from 1000 to 75,000, wherein the lubricating composition has a SAE viscosity grade from XW-Y, wherein X is from 0 to 20 and Y is from 20 to 50; and wherein the lubricating composition has a phosphorus content from a metal hydrocarbyl dithiophosphate of 0.12 wt % or less.
- the internal combustion engine is suitable for motorcycles for example motorcycles with a 4-stroke internal combustion engine.
- Oils of lubricating viscosity may also be defined as specified in the American Petroleum Institute (API) Base Oil Interchangeability Guidelines.
- the oil of lubricating viscosity comprises an API Group I, II, III, IV, V, VI oil or mixtures thereof, and in another embodiment API Group II, III, IV oil or mixtures thereof.
- the oil of lubricating viscosity is a Group III or IV base oil and in another embodiment a Group IV base oil. If the oil of lubricating viscosity is an API Group II, III, IV, V or VI oil there may be up to 40 wt % and in another embodiment up to a maximum of 5 wt % of the lubricating oil an API Group I oil present.
- Y is chosen from 20, 25, 30, 35, 40, 45 or 50.
- the oil of lubricating viscosity in one embodiment is present from 2 wt % to 99.5 wt % of the lubricating composition, in another embodiment from 29 wt % to 98.25 wt % of the lubricating composition and in another embodiment from 40 wt % to 97 wt % of the lubricating composition.
- suitable amounts of an oil of lubricating viscosity include 55 wt %, 60 wt %, 65 wt %, 70 wt %, 75 wt % or 80 wt %.
- the viscosity modifier in one embodiment is present from 0.5 wt % to 95 wt %, in another embodiment 0.75 wt % to 70 wt % and in another embodiment 1 wt % to 40 wt % of the lubricating composition.
- a suitable amount of viscosity modifier include 8 wt %, 10 wt %, 12 wt %, 14 wt %, 16 wt %, 18 wt %, 20 wt %, 22 wt %, 24 wt %, 30 wt %, 35 wt %, or 55 wt %.
- the viscosity modifiers (which may also be dispersant viscosity modifiers, as further described below) are known in the art and commercially available from a number of corporations, including The Lubrizol Corporation, Degussa AG and Rohmax GmbH.
- the viscosity modifier has a Shear Stability Index (SSI) as determined by CEC L-45-A-99 of 22 or less, 20 or less or 18 or less.
- SSI Shear Stability Index
- the viscosity SSI is 2 or more or 4 or more. Examples of suitable ranges of SSI include 2 to 22 or 4 to 18.
- the poly(meth)acrylate polymeric dispersant viscosity modifier includes a copolymer derived from a (meth)acrylate monomer containing an alkyl group with 1 to 30 carbon atoms, in another embodiment 1 to 26 carbon atoms and in another embodiment 1 to 20 carbon atoms.
- the alkyl group includes mixtures derived from an alcohol containing 1 to 4 carbon atoms, 8 to 10 carbon atoms, 12 to 14 carbon atoms, 12 to 15 carbon atoms, 16 to 18 carbon atoms or 16 to 20 carbon atoms. Examples of commercially available alcohol mixtures include the following products sold under the brand names of DobanolTM 25, NeodolTM 25, LialTM 125, and AlchemTM 125. In one embodiment the alcohol is a single alcohol, i.e., not a mixture.
- the (meth)acrylate monomer includes those derived from natural or synthetic sources. When derived by synthetic sources the (meth)acrylate monomer may be prepared using known direct esterification and/or transesterification processes.
- Upper limits on the amount of methyl (meth)acrylate include 40 wt % of the poly(meth)acrylate, in another embodiment 30 wt% of the poly(meth)acrylate and in another embodiment 20 wt % of the poly(meth)acrylate.
- the composition further contains a metal hydrocarbyl dithiophosphate.
- the amount of the metal hydrocarbyl dithiophosphate present is enough to provide a phosphorus content in the lubricating composition from said metal hydrocarbyl dithiophosphate of 0.12 wt % or less.
- the phosphorus content in the lubricating composition from a metal hydrocarbyl dithiophosphate is below 0.1 wt %, in another embodiment below 0.085 wt %, in another embodiment below 0.06 wt % or lower.
- the lower limit of the phosphorus content in the lubricating composition from a metal hydrocarbyl dithiophosphate is 0 ppm or higher, in another embodiment 50 ppm or higher, in another embodiment 125 ppm or higher and in another embodiment 200 ppm or higher. Examples of suitable ranges include 50 ppm to 0.1 wt % or 125 ppm to 0.085 wt %.
- Examples of a metal hydrocarbyl dithiophosphate include zinc dihydrocarbyl dithiophosphates (often referred to as ZDDP, ZDP or ZDTP).
- ZDDP zinc dihydrocarbyl dithiophosphates
- ZDP zinc dihydrocarbyl dithiophosphates
- ZDTP zinc dihydrocarbyl dithiophosphates
- the number of carbon atoms of each hydrocarbyl group is 2 to 30, 3 to 14 or 4 to 10.
- Suitable zinc hydrocarbyl dithiophosphates compounds may include those with a hydrocarbyl group of octyl, 2-ethylhexyl, methylpentyl-isopropyl. 2-ethylhexyl-isopropyl, pentyl-isobutyl or mixtures thereof.
- the composition optionally includes at least one additional performance additive.
- the additional performance additive includes at least one of metal deactivators, detergents, dispersants, extreme pressure agents, antiwear agents, antioxidants, corrosion inhibitors, foam inhibitors, demulsifiers, pour point depressants, friction modifiers, seal swelling agents and mixtures thereof.
- the additional performance additives may be used alone or in combination.
- the total combined amount of the other performance additive compounds present ranges from 0 wt % to 30 wt %, in another embodiment from 1 wt % to 25 wt % and in another embodiment 2 wt % to 20 wt % or from 3 wt % to 10 wt % of the lubricating composition.
- the other performance additives may be present, it is common for the other additional performance additives to be present in different amounts relative to each other.
- Detergents include neutral or overbased, Newtonian or non-Newtonian, basic salts of alkali, alkaline earth and transition metals with one or more of a phenate, a sulphurised phenate, a sulphonate, a carboxylic acid, a phosphorus acid, a mono- and/or a di- thiophosphoric acid, a saligenin, an alkylsalicylate, a salixarate or mixtures thereof.
- Dispersants include N-substituted long chain alkenyl succinimide as well as post-treated versions thereof.
- Post-treated dispersants include those further treated by reaction with materials such as urea, boron, thiourea, dimercaptothiadiazoles, carbon disulphide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, nitriles, epoxides and phosphorus compounds.
- Lubricating compositions are prepared by blending additives as shown in Table 1 into a 10W-40 lubricant.
- the lubricating compositions have a phosphorus content in the lubricating composition from a metal hydrocarbyl dithiophosphate of less than 0.12 wt %.
- the compositions prepared are: Table 1 Example Polymer Type Number Average Molecular Weight REF1 Commercially available Olefin copolymer Over 100,000 REF2 Commercially available Olefin copolymer 84,000 EX1 Polymethacrylate 15,000
- the presence of the viscosity modifier with a number average molecular weight from 1000 to 75,000 has acceptable shear stability and is suitable for viscosity control in an internal combustion engine comprising a crankcase and at least one of a gear and a wet-clutch. Further, the viscosity modifier is capable of imparting at least one of wear control, acceptable fuel economy, acceptable high temperature viscometrics and increased lubricant oil service drains. Furthermore, the results indicate that a polymer with a low Shear Stability Index of 26 and a number average molecular weight of above 75,000 provides poor a viscosity control performance.
- hydrocarbyl substituent or “hydrocarbyl group,” as used herein are used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group primarily composed of carbon and hydrogen atoms and attached to the remainder of the molecule through a carbon atom and which does not exclude the presence of other atoms or groups in a proportion insufficient to detract from the molecule having a predominantly hydrocarbon character. In general, no more than two, in one aspect no more than one, non-hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; typically, there will be no non-hydrocarbon substituents in the hydrocarbyl group. A more detailed definition of the terms “hydrocarbyl substituent” or “hydrocarbyl group,” is provided in US Patent Number 6,583,092 .
- each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, by-products, derivatives, and other such materials which are normally understood to be present in the commercial grade. It is to be understood that the upper and lower amount, range, and ratio limits set forth herein may be independently combined. Similarly, the ranges and amounts for each element of the invention may be used together with ranges or amounts for any of the other elements.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Claims (11)
- Verfahren zum Schmieren eines Verbrennungsmotors, der ein Kurbelwellengehäuse sowie ein Getriebe und/oder eine Nasskupplung umfasst, wobei das Verfahren das Zuführen einer schmierenden Zusammensetzung zu dem Kurbelwellengehäuse und zu dem Getriebe und/oder der Nasskupplung umfasst, die Folgendes umfasst:(a) ein Öl mit schmierender Viskosität und(b) einen Viskositätsmodifizierer mit einem zahlengemittelten Molekulargewicht von 1000 bis 75.000, wobei es sich bei dem Viskositätsmodifizierer um ein Poly(meth)acrylat handelt, wobei der Viskositätsmodifizierer einen mittels CEC L-45-A-99 bestimmten Scherstabilitätsindex (SSI) von 22 oder weniger aufweist,wobei die schmierende Zusammensetzung einen SAE-Viskositätsgrad von XW-Y aufweist, wobei X 0 bis 20 ist und Y 20 bis 50 ist, und wobei die schmierende Zusammensetzung einen Phosphorgehalt aus einem Metallhydrocarbyldithiophosphat von 0,12 Gew.-% oder weniger aufweist, wobei es sich bei dem Verbrennungsmotor um einen Viertakt-Motorradmotor handelt.
- Verfahren nach Anspruch 1, wobei der Verbrennungsmotor ein allgemeines Ölreservoir aufweist, aus dem dieselbe schmierende Zusammensetzung dem Kurbelwellengehäuse und dem Getriebe und/oder der Nasskupplung zugeführt wird.
- Verfahren nach Anspruch 1, wobei die schmierende Zusammensetzung dem Kurbelwellengehäuse und dem Getriebe oder mehreren Getrieben zugeführt wird.
- Verfahren nach Anspruch 1, wobei die schmierende Zusammensetzung dem Kurbelwellengehäuse und der Nasskupplung zugeführt wird.
- Verfahren nach Anspruch 1, wobei die schmierende Zusammensetzung dem Kurbelwellengehäuse und sowohl dem Getriebe (bzw. den Getrieben) als auch der Nasskupplung zugeführt wird.
- Verfahren nach Anspruch 1, wobei der Viskositätsmodifizierer ein zahlengemitteltes Molekulargewicht von 2000 bis 60.000 oder von 8000 bis 40.000 aufweist.
- Verfahren nach Anspruch 1, wobei der Viskositätsmodifizierer ein zahlengemitteltes Molekulargewicht von 1000 bis 20.000 oder von 25.000 bis 40.000 aufweist.
- Verfahren nach Anspruch 1, wobei es sich bei dem Viskositätsmodifizierer um ein funktionalisiertes Poly(meth)acrylat handelt.
- Verfahren nach Anspruch 8, wobei das Poly(meth)acrylat mit einem stickstoffhaltigen Monomer funktionalisiert ist.
- Verfahren nach Anspruch 1, wobei der Viskositätsmodifizierer in einer Menge von 0,5 Gew.-% bis 95 Gew.-% oder 1 Gew.-% bis 40 Gew.-% der schmierenden Zusammensetzung vorhanden ist.
- Verfahren nach Anspruch 1, wobei der Viskositätsmodifizierer einen mittels CEC L-45-A-99 bestimmten Scherstabilitätsindex (SSI) von 4 bis 18 aufweist.
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US63843704P | 2004-12-22 | 2004-12-22 | |
PCT/US2005/044925 WO2006068866A1 (en) | 2004-12-22 | 2005-12-13 | Method of viscosity control |
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EP1844128A1 EP1844128A1 (de) | 2007-10-17 |
EP1844128B1 true EP1844128B1 (de) | 2017-11-08 |
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EP05853765.5A Active EP1844128B1 (de) | 2004-12-22 | 2005-12-13 | Verfahren zur regulierung der viskosität |
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EP (1) | EP1844128B1 (de) |
JP (1) | JP5004237B2 (de) |
CN (1) | CN101120077B (de) |
ES (1) | ES2648996T3 (de) |
WO (1) | WO2006068866A1 (de) |
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DE102009001301A1 (de) * | 2008-03-11 | 2009-09-24 | Volkswagen Ag | Verfahren zum Schmieren einer Komponente nur für die Kupplung eines automatischen Getriebes, welche Schmierung erfordert |
WO2009125075A1 (fr) * | 2008-04-11 | 2009-10-15 | Total Raffinage Marketing | Fluide lubrifiant multifonctionnel |
EP2333037A4 (de) | 2008-09-19 | 2012-03-21 | Idemitsu Kosan Co | Schmierölzusammensetzung für einen verbrennungsmotor |
DE102010028195A1 (de) | 2010-04-26 | 2011-10-27 | Evonik Rohmax Additives Gmbh | Schmiermittel für Getriebe |
EP2705127A1 (de) | 2011-05-04 | 2014-03-12 | The Lubrizol Corporation | Motorschmiermittel für motorrad |
SG11201401409QA (en) * | 2011-11-01 | 2014-06-27 | Exxonmobil Res & Eng Co | Lubricants with improved low-temperature fuel economy |
CN106661494B (zh) | 2014-06-18 | 2020-06-12 | 路博润公司 | 摩托车发动机润滑剂 |
JP2017066220A (ja) * | 2015-09-29 | 2017-04-06 | Jxエネルギー株式会社 | 潤滑油組成物 |
US20180148663A1 (en) | 2016-11-30 | 2018-05-31 | Chevron Japan Ltd. | Lubricating oil compositions for motorcycles |
JP6927488B2 (ja) * | 2017-03-30 | 2021-09-01 | 出光興産株式会社 | 二輪車用潤滑油組成物、該潤滑油組成物を用いた二輪車の燃費向上方法、及び該潤滑油組成物の製造方法 |
GB201718527D0 (en) | 2017-11-09 | 2017-12-27 | Croda Int Plc | Lubricant formulation & friction modifier additive |
CN114276856B (zh) * | 2021-12-29 | 2022-12-30 | 金丰宏润科技(广东)有限公司 | 一种全合成酯类摩托车油及其制备方法 |
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DE1248643B (de) * | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
US3835053A (en) * | 1972-11-13 | 1974-09-10 | Shell Oil Co | Lubricating compositions |
US4234435A (en) * | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
US5112509A (en) | 1988-12-22 | 1992-05-12 | Texaco, Inc. | Non-dispersant, shear-stabilizing, and wear-inhibiting viscosity index improver |
JPH04282054A (ja) * | 1991-03-07 | 1992-10-07 | Suzuki Motor Corp | 自動二輪車のエンジン潤滑回路 |
US6004910A (en) * | 1994-04-28 | 1999-12-21 | Exxon Chemical Patents Inc. | Crankcase lubricant for modern heavy duty diesel and gasoline fueled engines |
US5789355A (en) * | 1995-06-06 | 1998-08-04 | Exxon Chemical Limited | Low volatility lubricating compositions |
US6124249A (en) * | 1998-12-22 | 2000-09-26 | The Lubrizol Corporation | Viscosity improvers for lubricating oil compositions |
US6408812B1 (en) * | 2000-09-19 | 2002-06-25 | The Lubrizol Corporation | Method of operating spark-ignition four-stroke internal combustion engine |
US6455477B1 (en) * | 2000-12-11 | 2002-09-24 | Infineum International Ltd. | Two-cycle lubricating oil with reduced smoke generation |
US20030013623A1 (en) * | 2001-05-01 | 2003-01-16 | Kwok-Leung Tse | Olefin copolymer viscocity index improvers |
US6583092B1 (en) | 2001-09-12 | 2003-06-24 | The Lubrizol Corporation | Lubricating oil composition |
MY128504A (en) * | 2001-09-25 | 2007-02-28 | Pennzoil Quaker State Co | Environmentally friendly lubricants |
AU2003278888A1 (en) * | 2002-09-30 | 2004-04-23 | Shell Internationale Research Maatschappij B.V. | Continuously variable transmission fluid and method of making same |
JP2005030304A (ja) * | 2003-07-14 | 2005-02-03 | Yamaha Motor Co Ltd | ドライサンプ形4サイクルエンジンの潤滑装置 |
JP2007514040A (ja) * | 2003-12-12 | 2007-05-31 | ザ ルブリゾル コーポレイション | スクシンイミド分散剤を含有する潤滑組成物 |
-
2005
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- 2005-12-13 ES ES05853765.5T patent/ES2648996T3/es active Active
- 2005-12-13 EP EP05853765.5A patent/EP1844128B1/de active Active
- 2005-12-13 JP JP2007548277A patent/JP5004237B2/ja not_active Expired - Fee Related
- 2005-12-13 WO PCT/US2005/044925 patent/WO2006068866A1/en active Application Filing
- 2005-12-13 US US11/722,368 patent/US20080096778A1/en not_active Abandoned
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2010
- 2010-05-04 US US12/773,150 patent/US20100212624A1/en not_active Abandoned
Non-Patent Citations (1)
Title |
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None * |
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WO2006068866A9 (en) | 2008-02-21 |
WO2006068866A1 (en) | 2006-06-29 |
JP5004237B2 (ja) | 2012-08-22 |
US20080096778A1 (en) | 2008-04-24 |
US20100212624A1 (en) | 2010-08-26 |
ES2648996T3 (es) | 2018-01-09 |
CN101120077B (zh) | 2012-07-04 |
CN101120077A (zh) | 2008-02-06 |
EP1844128A1 (de) | 2007-10-17 |
JP2008525583A (ja) | 2008-07-17 |
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