CN101087823A - 星形聚合物及其组合物 - Google Patents
星形聚合物及其组合物 Download PDFInfo
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- CN101087823A CN101087823A CNA2005800447279A CN200580044727A CN101087823A CN 101087823 A CN101087823 A CN 101087823A CN A2005800447279 A CNA2005800447279 A CN A2005800447279A CN 200580044727 A CN200580044727 A CN 200580044727A CN 101087823 A CN101087823 A CN 101087823A
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- alkyl
- methyl
- group
- star polymer
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- 229920000642 polymer Polymers 0.000 title claims abstract description 150
- 239000000203 mixture Substances 0.000 title claims abstract description 133
- 239000000178 monomer Substances 0.000 claims abstract description 92
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 87
- -1 acrylate ester Chemical class 0.000 claims abstract description 77
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 37
- 150000002367 halogens Chemical class 0.000 claims abstract description 37
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 32
- 150000003254 radicals Chemical class 0.000 claims abstract description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 31
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 19
- 125000000524 functional group Chemical group 0.000 claims abstract description 18
- 230000001050 lubricating effect Effects 0.000 claims abstract description 18
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 125000004429 atom Chemical group 0.000 claims abstract description 12
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
- 239000001301 oxygen Substances 0.000 claims abstract description 10
- 230000007246 mechanism Effects 0.000 claims abstract description 9
- 239000000126 substance Substances 0.000 claims description 88
- 229910052799 carbon Inorganic materials 0.000 claims description 75
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 58
- 239000003921 oil Substances 0.000 claims description 57
- 238000005461 lubrication Methods 0.000 claims description 36
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 30
- 238000006116 polymerization reaction Methods 0.000 claims description 26
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 238000005516 engineering process Methods 0.000 claims description 23
- DOTMOQHOJINYBL-UHFFFAOYSA-N molecular nitrogen;molecular oxygen Chemical compound N#N.O=O DOTMOQHOJINYBL-UHFFFAOYSA-N 0.000 claims description 20
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 18
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 13
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 13
- 239000000654 additive Substances 0.000 claims description 13
- 230000000996 additive effect Effects 0.000 claims description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 12
- 239000007822 coupling agent Substances 0.000 claims description 12
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 12
- 230000008569 process Effects 0.000 claims description 12
- 150000001412 amines Chemical class 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 229910052698 phosphorus Inorganic materials 0.000 claims description 10
- 239000011574 phosphorus Substances 0.000 claims description 10
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
- 239000012530 fluid Substances 0.000 claims description 9
- 239000003999 initiator Substances 0.000 claims description 9
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 239000005864 Sulphur Substances 0.000 claims description 8
- 239000006185 dispersion Substances 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
- 239000007788 liquid Substances 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 claims description 8
- 229920000768 polyamine Polymers 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 239000012208 gear oil Substances 0.000 claims description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 7
- 229910052723 transition metal Inorganic materials 0.000 claims description 7
- 150000003624 transition metals Chemical class 0.000 claims description 7
- 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 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 230000005540 biological transmission Effects 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 239000007859 condensation product Substances 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 239000003446 ligand Substances 0.000 claims description 5
- 239000010687 lubricating oil Substances 0.000 claims description 5
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 230000000379 polymerizing effect Effects 0.000 claims description 5
- 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 4
- 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 4
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims description 4
- 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 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 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 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 238000002485 combustion reaction Methods 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 230000000994 depressogenic effect Effects 0.000 claims description 4
- 239000000839 emulsion Substances 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000003112 inhibitor Substances 0.000 claims description 4
- 238000012546 transfer Methods 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
- 125000001118 alkylidene group Chemical group 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 150000001733 carboxylic acid esters Chemical class 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 claims description 3
- 230000007797 corrosion Effects 0.000 claims description 3
- 125000004386 diacrylate group Chemical group 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 239000011630 iodine Substances 0.000 claims description 3
- 238000000746 purification Methods 0.000 claims description 3
- 238000010526 radical polymerization reaction Methods 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 230000008961 swelling Effects 0.000 claims description 3
- 125000002769 thiazolinyl group Chemical group 0.000 claims description 3
- KFQPRNVTVMCYEH-UHFFFAOYSA-N 1-amino-3-(4-methoxyphenoxy)propan-2-ol Chemical compound COC1=CC=C(OCC(O)CN)C=C1 KFQPRNVTVMCYEH-UHFFFAOYSA-N 0.000 claims description 2
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims description 2
- MFGALGYVFGDXIX-UHFFFAOYSA-N 2,3-Dimethylmaleic anhydride Chemical compound CC1=C(C)C(=O)OC1=O MFGALGYVFGDXIX-UHFFFAOYSA-N 0.000 claims description 2
- PUGOMSLRUSTQGV-UHFFFAOYSA-N 2,3-di(prop-2-enoyloxy)propyl prop-2-enoate Chemical compound C=CC(=O)OCC(OC(=O)C=C)COC(=O)C=C PUGOMSLRUSTQGV-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 2
- AXGOOCLYBPQWNG-UHFFFAOYSA-N 3-ethylfuran-2,5-dione Chemical compound CCC1=CC(=O)OC1=O AXGOOCLYBPQWNG-UHFFFAOYSA-N 0.000 claims description 2
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 claims description 2
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 claims description 2
- ZWAPMFBHEQZLGK-UHFFFAOYSA-N 5-(dimethylamino)-2-methylidenepentanamide Chemical compound CN(C)CCCC(=C)C(N)=O ZWAPMFBHEQZLGK-UHFFFAOYSA-N 0.000 claims description 2
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- 239000005069 Extreme pressure additive Substances 0.000 claims description 2
- 229930195725 Mannitol Natural products 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 2
- 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 2
- MDMKOESKPAVFJF-UHFFFAOYSA-N [4-(2-methylprop-2-enoyloxy)phenyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=C(OC(=O)C(C)=C)C=C1 MDMKOESKPAVFJF-UHFFFAOYSA-N 0.000 claims description 2
- 125000002723 alicyclic group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims description 2
- 125000005647 linker group Chemical group 0.000 claims description 2
- 239000000594 mannitol Substances 0.000 claims description 2
- 235000010355 mannitol Nutrition 0.000 claims description 2
- CKIBIKFBPKFOQX-UHFFFAOYSA-N n-butyl-n',n'-dimethylprop-2-enehydrazide Chemical compound CCCCN(N(C)C)C(=O)C=C CKIBIKFBPKFOQX-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 229920001610 polycaprolactone Polymers 0.000 claims description 2
- 239000004632 polycaprolactone Substances 0.000 claims description 2
- FAIDIRVMPHBRLT-UHFFFAOYSA-N propane-1,2,3-triol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OCC(O)CO FAIDIRVMPHBRLT-UHFFFAOYSA-N 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 2
- 101710141544 Allatotropin-related peptide Proteins 0.000 claims 2
- 150000008064 anhydrides Chemical class 0.000 claims 2
- 239000004034 viscosity adjusting agent Substances 0.000 abstract description 10
- 239000002270 dispersing agent Substances 0.000 abstract 2
- 239000002243 precursor Substances 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 description 52
- 150000002148 esters Chemical class 0.000 description 34
- 239000002585 base Substances 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 20
- 239000002253 acid Substances 0.000 description 18
- 229920001577 copolymer Polymers 0.000 description 17
- 230000008859 change Effects 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 13
- ZGRWZUDBZZBJQB-UHFFFAOYSA-N benzenecarbodithioic acid Chemical compound SC(=S)C1=CC=CC=C1 ZGRWZUDBZZBJQB-UHFFFAOYSA-N 0.000 description 12
- 238000012712 reversible addition−fragmentation chain-transfer polymerization Methods 0.000 description 12
- LDHQCZJRKDOVOX-UHFFFAOYSA-N 2-butenoic acid Chemical compound CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 10
- 229920000193 polymethacrylate Polymers 0.000 description 10
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000004793 Polystyrene Substances 0.000 description 6
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
- 238000010008 shearing Methods 0.000 description 6
- 239000012986 chain transfer agent Substances 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 230000009466 transformation Effects 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- 229920006222 acrylic ester polymer Polymers 0.000 description 4
- 125000005907 alkyl ester group Chemical group 0.000 description 4
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 4
- NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 4
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000012989 trithiocarbonate Substances 0.000 description 4
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 239000004435 Oxo alcohol Substances 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000008431 aliphatic amides Chemical class 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- ZCKPFAYILJKXAT-UHFFFAOYSA-N benzyl benzenecarbodithioate Chemical compound C=1C=CC=CC=1C(=S)SCC1=CC=CC=C1 ZCKPFAYILJKXAT-UHFFFAOYSA-N 0.000 description 3
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 3
- 229940073608 benzyl chloride Drugs 0.000 description 3
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 3
- 150000002924 oxiranes Chemical class 0.000 description 3
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000005077 polysulfide Substances 0.000 description 3
- 229920001021 polysulfide Polymers 0.000 description 3
- 150000008117 polysulfides Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 3
- 239000012991 xanthate Substances 0.000 description 3
- PTYXPKUPXPWHSH-UHFFFAOYSA-N 1-(butyltetrasulfanyl)butane Chemical compound CCCCSSSSCCCC PTYXPKUPXPWHSH-UHFFFAOYSA-N 0.000 description 2
- IUXIOXCOPJFKMQ-UHFFFAOYSA-N 2-bromo-4-methylpentane Chemical compound CC(C)CC(C)Br IUXIOXCOPJFKMQ-UHFFFAOYSA-N 0.000 description 2
- MONMFXREYOKQTI-UHFFFAOYSA-N 2-bromopropanoic acid Chemical compound CC(Br)C(O)=O MONMFXREYOKQTI-UHFFFAOYSA-N 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
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- RWIVICVCHVMHMU-UHFFFAOYSA-N n-aminoethylmorpholine Chemical compound NCCN1CCOCC1 RWIVICVCHVMHMU-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- 238000012705 nitroxide-mediated radical polymerization Methods 0.000 description 1
- AOAFIKNGZOOCRX-UHFFFAOYSA-N o-ethyl 1-phenylethylsulfanylmethanethioate Chemical compound CCOC(=S)SC(C)C1=CC=CC=C1 AOAFIKNGZOOCRX-UHFFFAOYSA-N 0.000 description 1
- HYURBBIIHCNUSC-UHFFFAOYSA-N o-ethyl cyanomethylsulfanylmethanethioate Chemical compound CCOC(=S)SCC#N HYURBBIIHCNUSC-UHFFFAOYSA-N 0.000 description 1
- DKKUKDFFFUHZPG-UHFFFAOYSA-N o-phenyl benzylsulfanylmethanethioate Chemical compound C=1C=CC=CC=1CSC(=S)OC1=CC=CC=C1 DKKUKDFFFUHZPG-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 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
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229910000065 phosphene Inorganic materials 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-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
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- HIZCIEIDIFGZSS-UHFFFAOYSA-L trithiocarbonate Chemical compound [S-]C([S-])=S HIZCIEIDIFGZSS-UHFFFAOYSA-L 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
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- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
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- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/005—Hyperbranched macromolecules
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- 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
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2438/00—Living radical polymerisation
- C08F2438/01—Atom Transfer Radical Polymerization [ATRP] or reverse ATRP
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- C08F2438/00—Living radical polymerisation
- C08F2438/03—Use of a di- or tri-thiocarbonylthio compound, e.g. di- or tri-thioester, di- or tri-thiocarbamate, or a xanthate as chain transfer agent, e.g . Reversible Addition Fragmentation chain Transfer [RAFT] or Macromolecular Design via Interchange of Xanthates [MADIX]
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/04—Broad molecular weight distribution, i.e. Mw/Mn > 6
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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
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
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- 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
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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
- C10M2217/024—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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- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/028—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
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Abstract
Description
实施例 | 臂的Mng/mol | Trigonox21wt% | 比例* | 臂平均数 | %** | 星形聚合物Mw(1000’s) | 星形聚合物Mn(1000’s) | PDI |
1 | 16,000 | 0.7 | 5∶1 | 2 | 8 | 48 | 47 | 1.02 |
2 | 16,000 | 0.7 | 10∶1 | 4 | 49 | 77 | 74 | 1.04 |
3 | 16,000 | 0.7 | 17∶1 | 7 | 78 | 133 | 104 | 1.28 |
4 | 20,000 | 0.5 | 10∶1 | 2 | 16 | 61 | 58 | 1.05 |
5 | 20,000 | 0.5 | 17∶1 | 4 | 57 | 101 | 83 | 1.22 |
6 | 20,000 | 0.5 | 25∶1 | 12 | 76 | 323 | 220 | 1.47 |
7 | 33,000 | 0.5 | 5∶1 | 3 | 20 | 87 | 84 | 1.04 |
8 | 33,000 | 0.3 | 10∶1 | 3 | 38 | 102 | 93 | 1.10 |
9 | 33,000 | 0.3 | 17∶1 | 5 | 68 | 190 | 160 | 1.19 |
10 | 33 000 | 0.3 | 25∶1 | 7 | 76 | 286 | 230 | 1.24 |
11 | 33,000 | 0.3 | 34∶1 | 10 | 79 | 378 | 294 | 1.29 |
12 | 54 000 | 0.2 | 17∶1 | 3 | 10 | 148 | 143 | 1.03 |
13 | 54,000 | 0.2 | 25∶1 | 6 | 66 | 378 | 304 | 1.24 |
14 | 54,000 | 0.2 | 34∶1 | 6 | 63 | 384 | 311 | 1.23 |
实施例 | 聚合物组成 |
15 | 70wt%甲基丙烯酸C12-C15酯;和30wt%甲基丙烯酸2-乙基己酯 |
16 | 80wt%甲基丙烯酸C12-C15酯;和20wt%甲基丙烯酸甲酯 |
17 | 90wt%甲基丙烯酸C12-C15酯;和10wt%甲基丙烯酸甲酯 |
18 | 70wt%甲基丙烯酸C12-C15酯;和30wt%甲基丙烯酸2-乙基己酯 |
19 | 70wt%甲基丙烯酸C12-C15酯;和30wt%甲基丙烯酸2-乙基己酯 |
实施例 | 臂的Mng/mol | T-21wt% | CTA/T-21比例 | 臂平均数 | 向星形聚合物的转化率% | 星形聚合物Mw(1000) | 星形聚合物Mn(x1000) | PDI |
15 | 15300 | 2.3 | 2/1 | 13 | 80 | 262.4 | 209.5 | 1.25 |
16 | 26900 | 0.4 | 2/1 | 8 | 76.5 | 253.3 | 181.3 | 1.4 |
17 | 31800 | 0.3 | 2/1 | 4.2 | 47 | 158.2 | 64.1 | 2.47 |
18 | 29600 | 0.12 | 5/1 | 11 | 76.8 | 467.6 | 365.6 | 1.28 |
19 | 21800 | 0.18 | 5/1 | 13 | 86.9 | 406 | 319 | 1.28 |
实施例 | VMD说明 | GPC | ||
Mn | Mw | PDI | ||
20 | PC12-15MA-b-PS(80∶20wt%) | 33600 | 39700 | 1.18 |
21 | PC12-15MA-b-PMMA(90∶10wt%) | 26200 | 22600 | 1.15 |
22 | PC12-15MA-b-PEHMA(70∶30wt%) | 32700 | 39000 | 1.19 |
23 | P(C12-15MA/2-EHMA)-b-PS(63∶27∶10wt%) | 30000 | 37100 | 1.23 |
24 | P(C12-15MA/2-EHMA)-b-PS(56∶24∶20wt%) | 27600 | 35200 | 1.27 |
25 | P(C12-15MA/MMA)-b-PS(64∶16∶20wt%) | 46500 | 52500 | 1.13 |
实施例 | 嵌段共聚物组成 |
26 | (甲基丙烯酸C12-C15酯)-b-(甲基丙烯酸甲酯)wt%比例80∶20 |
27 | (甲基丙烯酸C12-C15酯)-b-(甲基丙烯酸甲酯)wt%比例70∶30 |
28 | (甲基丙烯酸C12-C15酯-b-甲基丙烯酸2-乙基己酯)-b-(苯乙烯)wt%比例63∶27∶10 |
29 | (甲基丙烯酸C12-C15酯-b-甲基丙烯酸2-乙基己酯)-b-(苯乙烯)wt%比例56∶24∶20 |
实施例 | 臂的Mng/mol | T-21wt% | 臂平均数 | 向星形聚合物的转化率% | 星形聚合物Mw(1000) | 星形聚合物Mn(1000) | PDI |
26 | 26200 | 0.36 | 8 | 35 | 186.5 | 157.4 | 1.18 |
27 | 32700 | 0.29 | 8 | 55 | 373.3 | 289.9 | 1.29 |
28 | 30000 | 0.28 | 8 | 22 | 263.1 | 228.3 | 1.15 |
29 | 27600 | 0.28 | 9 | 38 | 363.8 | 311.2 | 1.17 |
实施例 | 臂平均数 | 星形聚合物Mw(1000的) | 星形聚合物Mn(1000的) | PDI |
30 | 12 | 24.04 | 14.87 | 1.62 |
聚合物臂的 聚合物组成(单体wt%) | ||||||||||
实施例 | A | B | C | D | 臂的Mng/mol | 臂平均数 | %** | 星形聚合物Mw(1000’s) | 星形聚合物Mn(1000’s) | PDI |
35 | 78.2 | 20 | 1.8 | 0 | 14,100 | 7 | 32 | 161.9 | 129.3 | 1.25 |
36 | 86 | 14 | 0 | 0 | 17,900 | 9 | 73 | 249 | 190.5 | 1.3 |
37 | 78.2 | 20 | 0 | 1.8 | 16,500 | 8 | 70 | 189.5 | 148.8 | 1.27 |
381 | 78.2 | 20 | 0 | 1.8 | 11,800 | 5 | 62 | 76.1 | 65.3 | 1.16 |
392 | 86 | 14 | 0 | 0 | 47,800 | 5 | 34 | 410.2 | 345 | 1.2 |
40 | 78.2 | 20 | 0 | 1.8 | 15,400 | 7 | 63 | 133.7 | 106 | 1.26 |
41 | 78.2 | 20 | 0 | 1.8 | 11,600 | 5 | 54 | 74.5 | 61.6 | 1.2 |
421 | 78.2 | 20 | 0 | 1.8 | 17,700 | 4 | 52 | 88.2 | 75.7 | 1.16 |
43 | 80 | 20 | 0 | 0 | 19,700 | 9 | 72 | 383.3 | 215.9 | 1.31 |
44 | 80 | 20 | 0 | 0 | 19,200 | 9 | 67 | 293.5 | 220.7 | 1.33 |
45 | 80 | 20 | 0 | 0 | 31,300 | 10 | 17 | 561.1 | 474.1 | 1.18 |
463 | 80 | 20 | 0 | 0 | 30,200 | 16 | 75 | 821.5 | 530.5 | 1.55 |
47 | 80 | 20 | 0 | 0 | 14,800 | 6 | 24 | 160.6 | 137.5 | 1.17 |
润滑组合物实施例 | 聚合物实施例 | 处理率(wt%) | BV-40(1000的) | KV100 | 粘度指数 |
1 | 1 | 16.7 | 10.6 | 8.55 | 189 |
2 | 2 | 15.4 | 10.4 | 9.01 | 201 |
3 | 3 | 17.1 | 12.4 | 12.29 | 230 |
4 | 4 | 22.1 | 16.2 | 11.64 | 205 |
5 | 5 | 17.1 | 13.2 | 12.8 | 227 |
6 | 6 | 13.8 | 10.8 | 13.49 | 248 |
7 | 7 | 13 | 12.6 | 11.08 | 214 |
8 | 8 | 14.4 | 13.4 | 10.98 | 209 |
9 | 9 | 10.4 | 11.2 | 11.24 | 225 |
10 | 10 | 9.5 | 10.4 | 11.49 | 231 |
11 | 11 | 9 | 9.95 | 11.82 | 239 |
12 | 12 | 11.7 | 11.4 | 10.94 | 218 |
13 | 13 | 7.7 | 10.4 | 11.25 | 229 |
14 | 14 | 8.7 | 10.4 | 12.49 | 238 |
油实施例 | 聚合物实施例 | 在KRL剪切实验后100℃下的运动粘度 | 剪切后的粘度损失 | 剪切稳定性指数(SSI) |
1 | 1 | 7.92 | 7.4 | 15.87 |
2 | 2 | 7.98 | 11.4 | 23.25 |
3 | 3 | 10.01 | 18.5 | 29.57 |
4 | 4 | 9.63 | 17.3 | 28.47 |
5 | 5 | 9.16 | 28.4 | 44.28 |
6 | 6 | 8.55 | 36.6 | 55.44 |
7 | 7 | 7.76 | 30.0 | 51.08 |
8 | 8 | 8.26 | 24.9 | 42.50 |
9 | 9 | 7.55 | 32.6 | 55.41 |
10 | 10 | 7.15 | 38.0 | 62.81 |
11 | 11 | 7.1 | 40.1 | 65.19 |
12 | 12 | 7.39 | 32.4 | 55.82 |
13 | 13 | 6.81 | 39.5 | 66.57 |
14 | 14 | 6.87 | 45.0 | 71.05 |
ATF实施例 | 聚合物实施例 | 处理率(wt%) | BV-40(1000的) | KV100 | 粘度指数 |
30 | 30 | 5.9 | 5.26 | 7.2 | 255 |
15 | 15 | 10.26 | -a- | 7.2 | 216 |
16 | 16 | 8.01 | 5.67 | 7.2 | 240 |
17 | 17 | 10 | 81.6 | 7.2 | 232 |
ATF实施例 | 聚合物实施例 | 在KRL剪切实验后100℃下的运动粘度 | 剪切后的粘度损失 | 剪切稳定性指数(SSI) |
15 | 15 | 6.0 | 14.5 | 31.4 |
16 | 16 | 5.85 | 21.9 | 35.3 |
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EP (1) | EP1833868B1 (zh) |
JP (2) | JP5078087B2 (zh) |
CN (1) | CN101087823B (zh) |
AU (1) | AU2005299676B2 (zh) |
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EP1833868A2 (en) | 2007-09-19 |
US20170058072A1 (en) | 2017-03-02 |
US10611871B2 (en) | 2020-04-07 |
US20070244018A1 (en) | 2007-10-18 |
CA2584744A1 (en) | 2006-05-04 |
WO2006047398A2 (en) | 2006-05-04 |
AU2005299676A1 (en) | 2006-05-04 |
EP1833868B1 (en) | 2013-04-17 |
JP2011246729A (ja) | 2011-12-08 |
CN101087823B (zh) | 2010-08-18 |
AU2005299676B2 (en) | 2011-02-10 |
US9522972B2 (en) | 2016-12-20 |
JP2008518052A (ja) | 2008-05-29 |
WO2006047398A3 (en) | 2006-08-10 |
CA2584744C (en) | 2013-09-24 |
JP5078087B2 (ja) | 2012-11-21 |
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