CN102977976B - 星形聚合物润滑组合物 - Google Patents
星形聚合物润滑组合物 Download PDFInfo
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- CN102977976B CN102977976B CN201210487178.4A CN201210487178A CN102977976B CN 102977976 B CN102977976 B CN 102977976B CN 201210487178 A CN201210487178 A CN 201210487178A CN 102977976 B CN102977976 B CN 102977976B
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- diacrylate
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- 239000000203 mixture Substances 0.000 title claims abstract description 184
- 230000001050 lubricating effect Effects 0.000 title claims abstract description 122
- 229920000642 polymer Polymers 0.000 title claims abstract description 64
- 150000002148 esters Chemical class 0.000 claims abstract description 92
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 53
- 239000011574 phosphorus Substances 0.000 claims abstract description 53
- 150000003839 salts Chemical class 0.000 claims abstract description 53
- 238000000034 method Methods 0.000 claims abstract description 45
- 239000002253 acid Substances 0.000 claims abstract description 42
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000002270 dispersing agent Substances 0.000 claims abstract description 28
- -1 alkyl methacrylate Chemical compound 0.000 claims description 165
- 239000000126 substance Substances 0.000 claims description 124
- 239000003795 chemical substances by application Substances 0.000 claims description 76
- 239000000178 monomer Substances 0.000 claims description 68
- 239000006185 dispersion Substances 0.000 claims description 49
- 125000000217 alkyl group Chemical group 0.000 claims description 42
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 35
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 34
- 239000000314 lubricant Substances 0.000 claims description 32
- 230000007246 mechanism Effects 0.000 claims description 32
- 229910052799 carbon Inorganic materials 0.000 claims description 31
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 31
- 150000001412 amines Chemical class 0.000 claims description 29
- 229920000193 polymethacrylate Polymers 0.000 claims description 28
- 239000003607 modifier Substances 0.000 claims description 24
- 230000005540 biological transmission Effects 0.000 claims description 23
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 19
- 229920002554 vinyl polymer Polymers 0.000 claims description 18
- 238000006116 polymerization reaction Methods 0.000 claims description 17
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- 238000010560 atom transfer radical polymerization reaction Methods 0.000 claims description 15
- 239000007822 coupling agent Substances 0.000 claims description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
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- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 claims description 13
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 13
- 229920002367 Polyisobutene Polymers 0.000 claims description 11
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 11
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 claims description 10
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
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- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 8
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 8
- 150000008431 aliphatic amides Chemical class 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 claims description 7
- 239000000047 product Substances 0.000 claims description 7
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 7
- GZBSIABKXVPBFY-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)CO GZBSIABKXVPBFY-UHFFFAOYSA-N 0.000 claims description 6
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 6
- 125000004386 diacrylate group Chemical group 0.000 claims description 6
- LGPAKRMZNPYPMG-UHFFFAOYSA-N (3-hydroxy-2-prop-2-enoyloxypropyl) prop-2-enoate Chemical compound C=CC(=O)OC(CO)COC(=O)C=C LGPAKRMZNPYPMG-UHFFFAOYSA-N 0.000 claims description 5
- OGBWMWKMTUSNKE-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C OGBWMWKMTUSNKE-UHFFFAOYSA-N 0.000 claims description 5
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 claims description 5
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 claims description 5
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 5
- 229930195725 Mannitol Natural products 0.000 claims description 5
- CQHKDHVZYZUZMJ-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-prop-2-enoyloxypropyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(CO)COC(=O)C=C CQHKDHVZYZUZMJ-UHFFFAOYSA-N 0.000 claims description 5
- 125000001118 alkylidene group Chemical group 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- 239000003925 fat Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 239000000594 mannitol Substances 0.000 claims description 5
- 235000010355 mannitol Nutrition 0.000 claims description 5
- 229920001610 polycaprolactone Polymers 0.000 claims description 5
- 239000004632 polycaprolactone Substances 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 239000007859 condensation product Substances 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 230000026731 phosphorylation Effects 0.000 claims description 4
- 238000006366 phosphorylation reaction Methods 0.000 claims description 4
- 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 description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- 150000001414 amino alcohols Chemical class 0.000 claims description 2
- 238000005885 boration reaction Methods 0.000 claims description 2
- OSPSWZSRKYCQPF-UHFFFAOYSA-N dibutoxy(oxo)phosphanium Chemical compound CCCCO[P+](=O)OCCCC OSPSWZSRKYCQPF-UHFFFAOYSA-N 0.000 claims description 2
- 150000002314 glycerols Chemical class 0.000 claims description 2
- 150000002462 imidazolines Chemical class 0.000 claims description 2
- 150000002632 lipids Chemical class 0.000 claims description 2
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 claims description 2
- 101710141544 Allatotropin-related peptide Proteins 0.000 claims 4
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- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical class S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 claims 3
- 150000002118 epoxides Chemical class 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 229960001860 salicylate Drugs 0.000 claims 1
- 239000003921 oil Substances 0.000 description 75
- 239000002585 base Substances 0.000 description 31
- 150000001721 carbon Chemical group 0.000 description 19
- 239000000654 additive Substances 0.000 description 14
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- 239000003446 ligand Substances 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000004215 Carbon black (E152) Substances 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 11
- 229930195733 hydrocarbon Natural products 0.000 description 11
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$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 11
- LDHQCZJRKDOVOX-UHFFFAOYSA-N 2-butenoic acid Chemical compound CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 10
- ZGRWZUDBZZBJQB-UHFFFAOYSA-N benzenecarbodithioic acid Chemical compound SC(=S)C1=CC=CC=C1 ZGRWZUDBZZBJQB-UHFFFAOYSA-N 0.000 description 10
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 10
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- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([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
- 238000003756 stirring Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
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- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
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- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- VZGDMQKNWNREIO-OUBTZVSYSA-N tetrachloromethane Chemical group Cl[13C](Cl)(Cl)Cl VZGDMQKNWNREIO-OUBTZVSYSA-N 0.000 description 1
- QHKIWQPIFXRUOW-UHFFFAOYSA-N tetracosan-1-amine Chemical group CCCCCCCCCCCCCCCCCCCCCCCCN QHKIWQPIFXRUOW-UHFFFAOYSA-N 0.000 description 1
- NCYNWQDLQJUTIY-UHFFFAOYSA-N tetradecyl but-2-enoate Chemical compound CCCCCCCCCCCCCCOC(=O)C=CC NCYNWQDLQJUTIY-UHFFFAOYSA-N 0.000 description 1
- JZALLXAUNPOCEU-UHFFFAOYSA-N tetradecylbenzene Chemical compound CCCCCCCCCCCCCCC1=CC=CC=C1 JZALLXAUNPOCEU-UHFFFAOYSA-N 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- VSAISIQCTGDGPU-UHFFFAOYSA-N tetraphosphorus hexaoxide Chemical compound O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
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- 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
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/085—Phosphorus oxides, acids or salts
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2209/084—Acrylate; Methacrylate
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- C10M2209/086—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 polycarboxylic, e.g. maleic acid
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- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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- C10M2215/08—Amides
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- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
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- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C10M2223/043—Ammonium or amine salts thereof
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- C10M2223/045—Metal containing thio derivatives
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- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
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- C10N2020/04—Molecular weight; Molecular weight distribution
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- C10N2020/073—Star shaped polymers
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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- C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
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- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
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- Chemical & Material Sciences (AREA)
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Abstract
Description
Claims (36)
Applications Claiming Priority (2)
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US74542206P | 2006-04-24 | 2006-04-24 | |
US60/745,422 | 2006-04-24 |
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CN2007800236351A Division CN101484557B (zh) | 2006-04-24 | 2007-04-12 | 星形聚合物润滑组合物 |
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CN102977976A CN102977976A (zh) | 2013-03-20 |
CN102977976B true CN102977976B (zh) | 2015-06-10 |
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CN2007800236351A Active CN101484557B (zh) | 2006-04-24 | 2007-04-12 | 星形聚合物润滑组合物 |
CN201210487178.4A Active CN102977976B (zh) | 2006-04-24 | 2007-04-12 | 星形聚合物润滑组合物 |
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CN2007800236351A Active CN101484557B (zh) | 2006-04-24 | 2007-04-12 | 星形聚合物润滑组合物 |
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US (1) | US9528070B2 (zh) |
EP (1) | EP2024469B1 (zh) |
JP (1) | JP5230604B2 (zh) |
CN (2) | CN101484557B (zh) |
AU (1) | AU2007243060B2 (zh) |
CA (1) | CA2650396C (zh) |
WO (1) | WO2007127615A2 (zh) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
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US20100099588A1 (en) | 2007-01-30 | 2010-04-22 | The Lubrizol Corporation | Dispersant Combination for Improved Transmission Fluids |
US8507422B2 (en) * | 2007-04-26 | 2013-08-13 | The Lubrizol Corporation | Antiwear polymer and lubricating composition thereof |
KR101775172B1 (ko) | 2009-06-04 | 2017-09-05 | 더루우브리졸코오포레이션 | 고 vi 점도 조정제로서의 폴리메타크릴레이트 |
FR2964115B1 (fr) * | 2010-08-27 | 2013-09-27 | Total Raffinage Marketing | Lubrifiant moteur |
WO2012030616A1 (en) | 2010-08-31 | 2012-03-08 | The Lubrizol Corporation | Star polymer and lubricating composition thereof |
EP3088498A1 (en) | 2011-12-30 | 2016-11-02 | The Lubrizol Corporation | Use of star polymers |
KR20150037750A (ko) * | 2012-07-24 | 2015-04-08 | 제이엑스 닛코닛세키에너지주식회사 | 폴리(메타)아크릴레이트계 점도 지수 향상제, 및 당해 점도 지수 향상제를 함유하는 윤활유 첨가제 및 윤활유 조성물 |
JP6018981B2 (ja) * | 2013-07-05 | 2016-11-02 | Jxエネルギー株式会社 | ポリ(メタ)アクリレート系粘度指数向上剤、並びに該粘度指数向上剤を含有する潤滑油添加剤及び潤滑油組成物 |
CN104395445A (zh) * | 2012-07-24 | 2015-03-04 | 吉坤日矿日石能源株式会社 | 聚(甲基)丙烯酸酯系粘度指数改进剂、以及含有该粘度指数改进剂的润滑油添加剂及润滑油组合物 |
JP6077954B2 (ja) * | 2013-07-05 | 2017-02-08 | Jxエネルギー株式会社 | ポリ(メタ)アクリレート系粘度指数向上剤、並びに該粘度指数向上剤を含有する潤滑油添加剤及び潤滑油組成物 |
JP6077955B2 (ja) * | 2013-07-05 | 2017-02-08 | Jxエネルギー株式会社 | ポリ(メタ)アクリレート系粘度指数向上剤、並びに該粘度指数向上剤を含有する潤滑油添加剤及び潤滑油組成物 |
US20150203782A1 (en) * | 2012-07-24 | 2015-07-23 | Jx Nippon Oil & Energy Corporation | Poly(meth)acrylate viscosity index improver, and lubricating oil composition and lubricating oil additive containing said viscosity index improver |
US9783757B2 (en) | 2012-07-24 | 2017-10-10 | Jx Nippon Oil & Energy Corporation | Poly(meth)acrylate-based viscosity index improver, lubricant additive and lubricant composition containing viscosity index improver |
JP6018982B2 (ja) * | 2013-07-05 | 2016-11-02 | Jxエネルギー株式会社 | ポリ(メタ)アクリレート系粘度指数向上剤、並びに該粘度指数向上剤を含有する潤滑油添加剤及び潤滑油組成物 |
CN104704014B (zh) * | 2012-08-20 | 2017-11-03 | 路博润公司 | 疏松核星型聚合物及其润滑组合物 |
US20160108337A1 (en) | 2013-05-14 | 2016-04-21 | The Lubrizol Corporation | Lubricating Composition and Method of Lubricating a Transmission |
US20190330553A1 (en) | 2016-06-17 | 2019-10-31 | Akzo Nobel Chemicals International B.V. | Lubricant spray polymers |
WO2017216332A1 (en) * | 2016-06-17 | 2017-12-21 | Akzo Nobel Chemicals International B.V. | Lubricant spray polymers |
CN109536266B (zh) * | 2017-09-21 | 2021-07-30 | 中国石油化工股份有限公司 | 一种降低润滑油酸值的处理方法 |
CN107828481B (zh) * | 2017-10-30 | 2021-08-17 | 江苏龙蟠科技股份有限公司 | 一种电动汽车变速箱用润滑油组合物及其制备方法 |
CN109762537A (zh) * | 2019-02-27 | 2019-05-17 | 郑州智锦电子科技有限公司 | 一种环境普适性多能效油田助剂的制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1321186A (zh) * | 1998-06-23 | 2001-11-07 | 美孚石油公司 | 衍生自选择性氢化聚合物的分散剂和分散剂粘度指数改进剂 |
CN1576359A (zh) * | 2003-07-01 | 2005-02-09 | 英菲诺姆国际有限公司 | 用于润滑油的粘度指数改进剂 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0439254A3 (en) | 1990-01-23 | 1992-02-12 | Rohm And Haas Company | Dispersant polymethacrylate viscosity index improvers |
GB9007267D0 (en) * | 1990-03-30 | 1990-05-30 | Shell Int Research | Process for preparing a dispersant/vi improver |
US5070131A (en) * | 1990-09-28 | 1991-12-03 | Shell Oil Company | Gear oil viscosity index improvers |
US5490945A (en) * | 1991-04-19 | 1996-02-13 | The Lubrizol Corporation | Lubricating compositions and concentrates |
DE4312715A1 (de) * | 1993-04-20 | 1994-10-27 | Roehm Gmbh | Kammpolymere |
JP2787417B2 (ja) * | 1994-06-02 | 1998-08-20 | 三洋化成工業株式会社 | 潤滑油組成物 |
US5665685A (en) * | 1994-06-02 | 1997-09-09 | Sanyo Chemical Industries, Ltd. | Gear and transmission lubricant compositions of improved sludge-dispersibility, fluids comprising the same |
US5552491A (en) | 1995-01-27 | 1996-09-03 | Ethyl Additives Corporation | Star-branched acrylate and methacrylate polymers |
EP0906342B2 (en) | 1996-06-12 | 2015-02-11 | Warwick Effect Polymers Limited | Polymerisation catalyst and process |
US6013735A (en) * | 1998-02-13 | 2000-01-11 | Ethyl Corporation | Process for the preparation of acrylate and methacrylate polymers |
US5955405A (en) * | 1998-08-10 | 1999-09-21 | Ethyl Corporation | (Meth) acrylate copolymers having excellent low temperature properties |
JP2001064286A (ja) * | 1999-08-25 | 2001-03-13 | New Japan Chem Co Ltd | 潤滑油組成物 |
US7034079B2 (en) * | 1999-10-20 | 2006-04-25 | The Lubrizol Corporation | Radial polymers prepared by stabilized free radical polymerization |
JP2002194372A (ja) * | 2000-12-25 | 2002-07-10 | Sanyo Chem Ind Ltd | 粘度指数向上剤および潤滑油組成物 |
JP4673487B2 (ja) * | 2001-02-02 | 2011-04-20 | Jx日鉱日石エネルギー株式会社 | 金属ベルト式無段変速機用潤滑油組成物 |
US6583092B1 (en) * | 2001-09-12 | 2003-06-24 | The Lubrizol Corporation | Lubricating oil composition |
US6586375B1 (en) * | 2002-04-15 | 2003-07-01 | The Lubrizol Corporation | Phosphorus salts of nitrogen containing copolymers and lubricants containing the same |
DE10314776A1 (de) | 2003-03-31 | 2004-10-14 | Rohmax Additives Gmbh | Schmierölzusammensetzung mit guten Reibeigenschaften |
US7297737B2 (en) * | 2003-08-13 | 2007-11-20 | E.I. Du Pont De Nemours And Company | Process for efficiently producing highly plasticized polyamide blends |
WO2005056739A1 (en) * | 2003-11-26 | 2005-06-23 | Arkema Inc. | Controlled radical acrylic copolymer thickeners |
US7439213B2 (en) * | 2004-10-19 | 2008-10-21 | The Lubrizol Corporation | Secondary and tertiary amines as friction modifiers for automatic transmission fluids |
US8513172B2 (en) * | 2004-10-25 | 2013-08-20 | The Lubrizol Corporation | Process for preparing polymers and compositions thereof |
US7906468B2 (en) * | 2005-02-23 | 2011-03-15 | Arkema Inc. | Acrylic block copolymer low temperature flow modifiers in lubricating oils |
-
2007
- 2007-04-12 CN CN2007800236351A patent/CN101484557B/zh active Active
- 2007-04-12 EP EP07760527.7A patent/EP2024469B1/en active Active
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1321186A (zh) * | 1998-06-23 | 2001-11-07 | 美孚石油公司 | 衍生自选择性氢化聚合物的分散剂和分散剂粘度指数改进剂 |
CN1576359A (zh) * | 2003-07-01 | 2005-02-09 | 英菲诺姆国际有限公司 | 用于润滑油的粘度指数改进剂 |
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WO2007127615A2 (en) | 2007-11-08 |
WO2007127615A3 (en) | 2008-01-10 |
JP2009534518A (ja) | 2009-09-24 |
CN101484557B (zh) | 2013-01-02 |
JP5230604B2 (ja) | 2013-07-10 |
AU2007243060B2 (en) | 2011-07-28 |
CN102977976A (zh) | 2013-03-20 |
CA2650396C (en) | 2015-05-26 |
CA2650396A1 (en) | 2007-11-08 |
CN101484557A (zh) | 2009-07-15 |
US20090209440A1 (en) | 2009-08-20 |
US9528070B2 (en) | 2016-12-27 |
AU2007243060A1 (en) | 2007-11-08 |
EP2024469A2 (en) | 2009-02-18 |
EP2024469B1 (en) | 2016-08-03 |
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