CN1926226A - 用于改善抗磨损保护的含有h桥形成官能团的聚合物 - Google Patents
用于改善抗磨损保护的含有h桥形成官能团的聚合物 Download PDFInfo
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- CN1926226A CN1926226A CNA2005800062609A CN200580006260A CN1926226A CN 1926226 A CN1926226 A CN 1926226A CN A2005800062609 A CNA2005800062609 A CN A2005800062609A CN 200580006260 A CN200580006260 A CN 200580006260A CN 1926226 A CN1926226 A CN 1926226A
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- Prior art keywords
- ester
- vinyl
- weight
- methyl
- methacrylic acid
- Prior art date
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- 230000004224 protection Effects 0.000 title claims abstract description 20
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- 239000000203 mixture Substances 0.000 claims abstract description 99
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- 125000000217 alkyl group Chemical group 0.000 claims abstract description 53
- 239000010687 lubricating oil Substances 0.000 claims abstract description 32
- 239000000654 additive Substances 0.000 claims abstract description 31
- 229920000578 graft copolymer Polymers 0.000 claims abstract description 21
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- -1 ester compound Chemical class 0.000 claims description 97
- 239000000126 substance Substances 0.000 claims description 78
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 77
- 229910052739 hydrogen Inorganic materials 0.000 claims description 58
- 239000001257 hydrogen Substances 0.000 claims description 57
- 238000000034 method Methods 0.000 claims description 49
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- 239000003795 chemical substances by application Substances 0.000 claims description 27
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 24
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 20
- 230000000996 additive effect Effects 0.000 claims description 20
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 15
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
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- 238000002360 preparation method Methods 0.000 claims description 10
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- 239000000463 material Substances 0.000 claims description 9
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 claims description 8
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- 230000015572 biosynthetic process Effects 0.000 claims description 8
- 238000010526 radical polymerization reaction Methods 0.000 claims description 8
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 6
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- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims description 5
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 claims description 5
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- LEWNYOKWUAYXPI-UHFFFAOYSA-N 1-ethenylpiperidine Chemical class C=CN1CCCCC1 LEWNYOKWUAYXPI-UHFFFAOYSA-N 0.000 claims description 4
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- LKLNVHRUXQQEII-UHFFFAOYSA-N 5-ethenyl-2,3-dimethylpyridine Chemical compound CC1=CC(C=C)=CN=C1C LKLNVHRUXQQEII-UHFFFAOYSA-N 0.000 claims description 4
- VCKHUTJVGJBGFO-UHFFFAOYSA-N C(=C)C=1NC=CN1.CC1=C(C(=O)O)C=CC=C1C(=O)O Chemical compound C(=C)C=1NC=CN1.CC1=C(C(=O)O)C=CC=C1C(=O)O VCKHUTJVGJBGFO-UHFFFAOYSA-N 0.000 claims description 4
- 125000001118 alkylidene group Chemical group 0.000 claims description 4
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 claims description 4
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 claims description 4
- 229920005604 random copolymer Polymers 0.000 claims description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 3
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- ZNAOFAIBVOMLPV-UHFFFAOYSA-N hexadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(C)=C ZNAOFAIBVOMLPV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- YOTGRUGZMVCBLS-UHFFFAOYSA-N pentadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCOC(=O)C(C)=C YOTGRUGZMVCBLS-UHFFFAOYSA-N 0.000 claims description 3
- KEROTHRUZYBWCY-UHFFFAOYSA-N tridecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C(C)=C KEROTHRUZYBWCY-UHFFFAOYSA-N 0.000 claims description 3
- 239000004711 α-olefin Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims 2
- ORNUPNRNNSVZTC-UHFFFAOYSA-N 2-vinylthiophene Chemical compound C=CC1=CC=CS1 ORNUPNRNNSVZTC-UHFFFAOYSA-N 0.000 claims 2
- ZWAPMFBHEQZLGK-UHFFFAOYSA-N 5-(dimethylamino)-2-methylidenepentanamide Chemical compound CN(C)CCCC(=C)C(N)=O ZWAPMFBHEQZLGK-UHFFFAOYSA-N 0.000 claims 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 24
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- GFNHASIYLNRZIC-UHFFFAOYSA-N phosphono 2-methyl-3-propylhex-2-enoate Chemical compound CCCC(CCC)=C(C)C(=O)OP(O)(O)=O GFNHASIYLNRZIC-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
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- 239000002798 polar solvent Substances 0.000 description 1
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- 229920001451 polypropylene glycol Polymers 0.000 description 1
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- 150000003141 primary amines Chemical class 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BVMNCGXSFZQPNI-UHFFFAOYSA-N prop-2-ynyl but-2-enoate Chemical compound CC=CC(=O)OCC#C BVMNCGXSFZQPNI-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical group CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
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- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- BWESROVQGZSBRX-UHFFFAOYSA-N pyrido[3,2-d]pyrimidine Chemical compound C1=NC=NC2=CC=CN=C21 BWESROVQGZSBRX-UHFFFAOYSA-N 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- XKXIQBVKMABYQJ-UHFFFAOYSA-N tert-butyl hydrogen carbonate Chemical compound CC(C)(C)OC(O)=O XKXIQBVKMABYQJ-UHFFFAOYSA-N 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- DIGWSCGMTNOSDZ-UHFFFAOYSA-N tetradec-13-enoic acid Chemical compound OC(=O)CCCCCCCCCCCC=C DIGWSCGMTNOSDZ-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
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Classifications
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- 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
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- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
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- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/16—Ethers
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- 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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- 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
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- C10M145/14—Acrylate; Methacrylate
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- 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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- C10M2209/084—Acrylate; Methacrylate
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- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/102—Polyesters
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/022—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
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- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/024—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
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- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/028—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
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- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/04—Molecular weight; Molecular weight distribution
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- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C10N2040/25—Internal-combustion engines
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- Graft Or Block Polymers (AREA)
Abstract
Description
油 | Paratone8002含量 | 聚丙烯酸酯各3重量% | CEC-L-51-A-98,凸轮磨损平均值100h后[μm] |
ABCDE | 11.5重量%8.5重量%8.5重量%8.5重量%8.5重量% | -对比实施例1对比实施例2实施例1实施例3 | 47.418.639.95.714.9 |
油 | Paratone80O2含量[重量%] | 聚丙烯酸酯各3重量% | KV40℃ | KV100℃ | VI | TBN | CCS | HTHS |
ABCDE | 11.58.58.58.58.5 | -对比实施例1对比实施例2实施例1实施例3 | 68.6167.1065.5566.44 | 11.3811.3811.5611.4411.50 | 161169171169 | 9.29.3n.b.n.b. | 44405225n.b.n.b. | 3.253.333.33n.b. |
油 | 聚丙烯酸酯 | 腐蚀 | |||
ASTM D 5968 | ASTM D 130 | ||||
Pb | Cu | Sn | Cu | ||
ABC | -对比实施例1对比实施例2 | 109.5120.0440.5 | 445 | 000 | 1b1b1b |
油 | 所用的聚合物溶液 | 重量%聚合物溶液 | 重量%KPE100 | 重量%APECore600 | 重量%PPD | 重量%Oloa4992 | 40℃的动力学粘度[cSt] | 100℃的动力学粘度[cSt] | 粘度指数(VI) |
FGHI | 实施例6对比实施例3-- | 6.96.9-- | 66.666.650.426 | 25.925.948.873.2 | --0.20.2 | 0.60.60.60.6 | 45.4746.2944.7468.28 | 7.9398.216.7878.787 | 146152105100 |
油F | 油G | 油H | 油I | |
工作压力(bar)容器中的液体温度(℃)输送流速(l/min)运行时间(h)物料改变环(mg)叶片(mg) | 140792625094 | 14080282502897 | 14074282503128 | 14085282501748 |
Claims (24)
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DE102004018094.6 | 2004-04-08 | ||
DE102004018094A DE102004018094A1 (de) | 2004-04-08 | 2004-04-08 | Polymere mit H-Brücken bildenden Funktionalitäten zur Verbesserung des Verschleißschutzes |
PCT/EP2005/001905 WO2005097956A1 (de) | 2004-04-08 | 2005-02-24 | POLYMERE MIT H-BRÜCKEN BILDENDEN FUNKTIONALITÄTEN ZUR VERBESSERUNG DES VERSCHLEIßSCHUTZES |
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CN1926226A true CN1926226A (zh) | 2007-03-07 |
CN1926226B CN1926226B (zh) | 2010-05-05 |
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US (1) | US8722600B2 (zh) |
EP (1) | EP1733011A1 (zh) |
JP (1) | JP4881293B2 (zh) |
KR (1) | KR101184484B1 (zh) |
CN (1) | CN1926226B (zh) |
BR (1) | BRPI0509664B1 (zh) |
CA (1) | CA2561175C (zh) |
DE (1) | DE102004018094A1 (zh) |
WO (1) | WO2005097956A1 (zh) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004034618A1 (de) * | 2004-07-16 | 2006-02-16 | Rohmax Additives Gmbh | Verwendung von Pfropfcopolymeren |
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FR2921517B1 (fr) * | 2007-09-26 | 2010-12-03 | Commissariat Energie Atomique | Membranes conductrices de protons pour pile a combustible presentant un gradient de protons et procedes de preparation desdites membranes |
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SG176054A1 (en) * | 2009-06-12 | 2011-12-29 | Evonik Rohmax Additives Gmbh | A fluid having improved viscosity index |
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EP2695932A1 (en) | 2012-08-08 | 2014-02-12 | Ab Nanol Technologies Oy | Grease composition |
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Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1694224A1 (de) | 1967-12-06 | 1971-07-22 | Hoechst Ag | Schwingungsgedaempfte Verbundsysteme mit Zwischenschichten aus Pfropfpolymerisaten von Styrol oder Styrol/Acrylsaeure auf Vinylacetat/2-AEthylhexylacrylat/Dibutylmaleinat/Crotonsaeure-Copolymerisaten |
US3554913A (en) * | 1969-08-15 | 1971-01-12 | Us Army | Friction reduction by copolymer of n-alkyl methacrylates and methacrylic acid in solution |
US3970725A (en) | 1972-09-26 | 1976-07-20 | Dai Nippon Toryo Co., Ltd. | Powdery coating composition and process for preparing the same |
JPS533423B2 (zh) | 1972-10-28 | 1978-02-06 | ||
IT1181905B (it) * | 1984-06-15 | 1987-09-30 | Anic Spa | Additivo multifunzionale per oli lubrificanti e procedimento per la sua preparazione |
US4916171A (en) | 1984-07-25 | 1990-04-10 | Rohm And Haas Company | Polymers comprising alkali-insoluble core/alkali-soluble shell and copositions thereof |
JPS61268610A (ja) * | 1985-05-24 | 1986-11-28 | G C Dental Ind Corp | 歯科用接着性補綴材料 |
CA2090200C (en) | 1992-03-20 | 2005-04-26 | Chung Y. Lai | Ashless dispersant polymethacrylate polymers |
FR2726828A1 (fr) | 1994-11-10 | 1996-05-15 | Rohm & Haas France | Additifs dispersants ameliorant l'indice de viscosite pour huiles lubrifiantes |
US5821313A (en) * | 1995-06-19 | 1998-10-13 | The Lubrizol Corporation | Dispersant-viscosity improvers for lubricating oil compositions |
US5969068A (en) | 1995-06-19 | 1999-10-19 | The Lubrizol Corporation | Dispersant-viscosity improvers for lubricating oil compositions |
EP1048711A1 (en) | 1999-03-03 | 2000-11-02 | Ethyl Petroleum Additives Limited | Lubricant compositions exhibiting improved demulse performance |
US6458750B1 (en) | 1999-03-04 | 2002-10-01 | Rohmax Additives Gmbh | Engine oil composition with reduced deposit-formation tendency |
US6610802B2 (en) * | 2001-05-29 | 2003-08-26 | Rohmax Additives Gmbh | Process for synthesis of polymer compositions, polymer compositionS obtainable by the process, and use of the same |
JP4605750B2 (ja) | 2002-03-01 | 2011-01-05 | エボニック ローマックス アディティヴス ゲゼルシャフト ミット ベシュレンクテル ハフツング | ロウ含有鉱油留出物を溶剤脱ロウするための添加剤の製造に適したコポリマーまたはポリマー混合物を含有する脱ロウ添加剤ならびにパラフィン含有の鉱油留出物を溶剤脱ロウする方法 |
US20040132629A1 (en) * | 2002-03-18 | 2004-07-08 | Vinci James N. | Lubricants containing olefin copolymer and acrylate copolymer |
WO2003080773A1 (fr) | 2002-03-27 | 2003-10-02 | Sanyo Chemical Industries, Ltd. | Regulateur de frottements pour huile de graissage et composition d'huile de graissage |
US20040077509A1 (en) | 2002-08-02 | 2004-04-22 | Tsuyoshi Yuki | Viscosity index improver and lube oil containing the same |
DE10249294A1 (de) | 2002-10-22 | 2004-05-13 | Rohmax Additives Gmbh | Stabile Polymerdispersionen und Verfahren zur Herstellung |
DE10249292A1 (de) | 2002-10-22 | 2004-05-13 | Rohmax Additives Gmbh | Polymerdispersionen mit geringer Viskosität und Verfahren zur Herstellung |
DE10249295A1 (de) | 2002-10-22 | 2004-05-13 | Rohmax Additives Gmbh | Polymerdispersionen mit hoher Stabilität und Verfahren zur Herstellung |
DE10314776A1 (de) * | 2003-03-31 | 2004-10-14 | Rohmax Additives Gmbh | Schmierölzusammensetzung mit guten Reibeigenschaften |
DE102004018093A1 (de) * | 2004-04-08 | 2005-10-27 | Rohmax Additives Gmbh | Polymere mit H-Brücken bildenden Funktionalitäten |
US7429555B2 (en) | 2004-04-30 | 2008-09-30 | Rohmax Additives Gmbh | Lubricating grease with high water resistance |
DE102005015931A1 (de) | 2005-04-06 | 2006-10-12 | Rohmax Additives Gmbh | Polyalkyl(meth) acrylat-Copolymere mit hervorragenden Eigenschaften |
US7648950B2 (en) | 2005-04-22 | 2010-01-19 | Rohmax Additives Gmbh | Use of a polyalkylmethacrylate polymer |
DE102005031244A1 (de) | 2005-07-01 | 2007-02-15 | Rohmax Additives Gmbh | Öllösliche Kammpolymere |
DE102005041528A1 (de) | 2005-08-31 | 2007-03-01 | Rohmax Additives Gmbh | Öllösliche Polymere |
DE102006016588A1 (de) | 2006-04-06 | 2007-10-18 | Rohmax Additives Gmbh | Kraftstoffzusammensetzungen umfassend nachwachsende Rohstoffe |
KR101492289B1 (ko) | 2007-07-09 | 2015-02-12 | 에보니크 오일 아디티페스 게엠베하 | 연료 소비를 감소시키기 위한 콤 중합체의 용도 |
DE102007036856A1 (de) | 2007-08-06 | 2009-02-26 | Evonik Rohmax Additives Gmbh | Verwendung von Estergruppen-umfassenden Polymeren als Antifatigue-Additive |
-
2004
- 2004-04-08 DE DE102004018094A patent/DE102004018094A1/de not_active Withdrawn
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- 2005-02-24 EP EP05715488A patent/EP1733011A1/de not_active Withdrawn
- 2005-02-24 WO PCT/EP2005/001905 patent/WO2005097956A1/de not_active Application Discontinuation
- 2005-02-24 KR KR1020067020797A patent/KR101184484B1/ko active IP Right Grant
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Cited By (5)
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CN109153935A (zh) * | 2016-05-18 | 2019-01-04 | 赢创油品添加剂有限公司 | 抗磨共聚物和润滑剂组合物 |
CN109153935B (zh) * | 2016-05-18 | 2021-10-29 | 赢创运营有限公司 | 抗磨共聚物和润滑剂组合物 |
CN109328226A (zh) * | 2016-06-17 | 2019-02-12 | 道达尔销售服务公司 | 润滑剂聚合物 |
CN114787327A (zh) * | 2019-12-12 | 2022-07-22 | 赢创运营有限公司 | 高粘度聚丙烯酸酯基础流体 |
CN114787327B (zh) * | 2019-12-12 | 2024-01-26 | 赢创运营有限公司 | 高粘度聚丙烯酸酯基础流体 |
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CN1926226B (zh) | 2010-05-05 |
WO2005097956A1 (de) | 2005-10-20 |
JP4881293B2 (ja) | 2012-02-22 |
KR101184484B1 (ko) | 2012-09-20 |
EP1733011A1 (de) | 2006-12-20 |
US8722600B2 (en) | 2014-05-13 |
DE102004018094A1 (de) | 2005-11-03 |
BRPI0509664B1 (pt) | 2015-11-03 |
CA2561175C (en) | 2013-10-01 |
JP2007532703A (ja) | 2007-11-15 |
US20070197409A1 (en) | 2007-08-23 |
KR20070034463A (ko) | 2007-03-28 |
WO2005097956A8 (de) | 2005-12-15 |
BRPI0509664A (pt) | 2007-10-09 |
CA2561175A1 (en) | 2005-10-20 |
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