TWI294896B - - Google Patents
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- TWI294896B TWI294896B TW092129172A TW92129172A TWI294896B TW I294896 B TWI294896 B TW I294896B TW 092129172 A TW092129172 A TW 092129172A TW 92129172 A TW92129172 A TW 92129172A TW I294896 B TWI294896 B TW I294896B
- Authority
- TW
- Taiwan
- Prior art keywords
- thermoplastic elastomer
- component
- elastomer composition
- polymer
- weight
- Prior art date
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- 229920002725 thermoplastic elastomer Polymers 0.000 claims abstract description 82
- 239000000203 mixture Substances 0.000 claims abstract description 70
- 229920000642 polymer Polymers 0.000 claims abstract description 69
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims abstract description 44
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 30
- 229920005989 resin Polymers 0.000 claims abstract description 27
- 239000011347 resin Substances 0.000 claims abstract description 27
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 23
- 150000001875 compounds Chemical class 0.000 claims abstract description 20
- -1 aromatic vinyl Compound Chemical class 0.000 claims description 63
- 238000006116 polymerization reaction Methods 0.000 claims description 28
- 239000004743 Polypropylene Substances 0.000 claims description 21
- 229920001155 polypropylene Polymers 0.000 claims description 21
- 150000001336 alkenes Chemical class 0.000 claims description 19
- 229920005672 polyolefin resin Polymers 0.000 claims description 18
- 229920001971 elastomer Polymers 0.000 claims description 16
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 16
- 229920001400 block copolymer Polymers 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 229920001903 high density polyethylene Polymers 0.000 claims description 8
- 239000004700 high-density polyethylene Substances 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 238000006467 substitution reaction Methods 0.000 claims description 6
- 239000000806 elastomer Substances 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 239000004902 Softening Agent Substances 0.000 claims description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 229920000428 triblock copolymer Polymers 0.000 claims description 2
- JSESLGVOWSWBSB-UHFFFAOYSA-N 1-(2-methylpropyl)-9h-fluorene Chemical compound C1C2=CC=CC=C2C2=C1C(CC(C)C)=CC=C2 JSESLGVOWSWBSB-UHFFFAOYSA-N 0.000 claims 1
- 241000736285 Sphagnum Species 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 229910021653 sulphate ion Inorganic materials 0.000 claims 1
- 239000012815 thermoplastic material Substances 0.000 claims 1
- 238000004132 cross linking Methods 0.000 abstract description 33
- 238000007906 compression Methods 0.000 abstract description 28
- 230000006835 compression Effects 0.000 abstract description 28
- 238000004898 kneading Methods 0.000 abstract description 10
- 238000013016 damping Methods 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 24
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 22
- 230000000052 comparative effect Effects 0.000 description 19
- 238000002156 mixing Methods 0.000 description 19
- 230000000704 physical effect Effects 0.000 description 14
- 239000003054 catalyst Substances 0.000 description 13
- 239000000178 monomer Substances 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 239000005060 rubber Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- 230000035939 shock Effects 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
- 239000003431 cross linking reagent Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 229920003023 plastic Polymers 0.000 description 8
- 239000004033 plastic Substances 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 239000001117 sulphuric acid Substances 0.000 description 7
- 235000011149 sulphuric acid Nutrition 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000002808 molecular sieve Substances 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 6
- 229920006132 styrene block copolymer Polymers 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- UHKPXKGJFOKCGG-UHFFFAOYSA-N 2-methylprop-1-ene;styrene Chemical compound CC(C)=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 UHKPXKGJFOKCGG-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 3
- 238000003723 Smelting Methods 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 239000004809 Teflon Substances 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 229920000092 linear low density polyethylene Polymers 0.000 description 3
- 239000004707 linear low-density polyethylene Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 229910052707 ruthenium Inorganic materials 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 3
- 238000001291 vacuum drying Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 229920005601 base polymer Polymers 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 235000011089 carbon dioxide Nutrition 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 230000000979 retarding effect Effects 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- 239000012748 slip agent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 239000000052 vinegar Substances 0.000 description 2
- 235000021419 vinegar Nutrition 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- YCTDZYMMFQCTEO-FNORWQNLSA-N (E)-3-octene Chemical compound CCCC\C=C\CC YCTDZYMMFQCTEO-FNORWQNLSA-N 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- ZRPAUEVGEGEPFQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2 ZRPAUEVGEGEPFQ-UHFFFAOYSA-N 0.000 description 1
- YJLUBHOZZTYQIP-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=N2 YJLUBHOZZTYQIP-UHFFFAOYSA-N 0.000 description 1
- PMAAOHONJPSASX-UHFFFAOYSA-N 2-butylperoxypropan-2-ylbenzene Chemical compound CCCCOOC(C)(C)C1=CC=CC=C1 PMAAOHONJPSASX-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- FKOZPUORKCHONH-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid Chemical compound CC(C)CS(O)(=O)=O FKOZPUORKCHONH-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
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- FCMDQPNIHLOMHL-UHFFFAOYSA-N 4-tert-butyldodecane Chemical compound CCCCCCCCC(CCC)C(C)(C)C FCMDQPNIHLOMHL-UHFFFAOYSA-N 0.000 description 1
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- PVMXUMGAUIMMFA-UHFFFAOYSA-N C1(=CCCCC1)OOC(C)(C)C Chemical compound C1(=CCCCC1)OOC(C)(C)C PVMXUMGAUIMMFA-UHFFFAOYSA-N 0.000 description 1
- YJOBGXITWVSGQV-UHFFFAOYSA-N CC(C)(C)OOC(C)(CCC(C)(OOC(C)(C)C)S)S Chemical compound CC(C)(C)OOC(C)(CCC(C)(OOC(C)(C)C)S)S YJOBGXITWVSGQV-UHFFFAOYSA-N 0.000 description 1
- LJUXHQWZXBCQJL-UHFFFAOYSA-N C[Ru](C)(C)C Chemical compound C[Ru](C)(C)C LJUXHQWZXBCQJL-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000241257 Cucumis melo Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 206010021703 Indifference Diseases 0.000 description 1
- 229910021638 Iridium(III) chloride Inorganic materials 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 244000147568 Laurus nobilis Species 0.000 description 1
- 235000017858 Laurus nobilis Nutrition 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 241000361919 Metaphire sieboldi Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- C08L23/22—Copolymers of isobutene; Butyl rubber; Homopolymers or copolymers of other iso-olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (4)
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| JP2002326407A JP4287126B2 (ja) | 2002-11-11 | 2002-11-11 | 熱可塑性エラストマー組成物 |
| JP2002376757A JP4287137B2 (ja) | 2002-12-26 | 2002-12-26 | 熱可塑性エラストマー組成物 |
| JP2003190111A JP4177186B2 (ja) | 2003-07-02 | 2003-07-02 | 熱可塑性エラストマー組成物 |
| JP2003191722A JP2005023244A (ja) | 2003-07-04 | 2003-07-04 | 熱可塑性エラストマー組成物 |
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| TW200420651A TW200420651A (en) | 2004-10-16 |
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| TWI263657B (en) * | 2002-12-23 | 2006-10-11 | Kaneka Corp | Thermoplastic elastomer composition |
| JP4473094B2 (ja) * | 2004-02-20 | 2010-06-02 | リケンテクノス株式会社 | 熱可塑性エラストマー組成物及びそれを用いた熱可塑性樹脂組成物 |
| JPWO2006095854A1 (ja) * | 2005-03-11 | 2008-08-21 | 株式会社カネカ | 防振材組成物 |
| EP2006328A4 (en) * | 2006-04-13 | 2011-03-02 | Kaneka Corp | COMPOSITION FOR RUBBER STOP AND RADIATION STOPPER FOR MEDICAL APPLICATION |
| WO2008045702A2 (en) * | 2006-10-05 | 2008-04-17 | Polyone Corporation | Thermoplastic elastomers of styrenic block copolymers and aliphatic thermoplastic polyurethanes |
| US7786217B2 (en) * | 2007-04-11 | 2010-08-31 | University Of Massachusetts Lowell | Organometallic-polyisomonoolefin block copolymers |
| EP2172515B1 (en) * | 2007-07-25 | 2012-06-06 | Daikyo Seiko, LTD. | Rubber compound and molded article |
| FR2938543B1 (fr) | 2008-11-19 | 2010-11-12 | Michelin Soc Tech | Nouveau copolymere a bloc elastomerique, son procede de preparation, son utilisation dans une composition elastomere |
| FR2939076B1 (fr) * | 2008-12-03 | 2011-10-21 | Michelin Soc Tech | Stratifie multicouche etanche a l'air pour objet pneumatique |
| FR2948320B1 (fr) | 2009-07-27 | 2011-07-29 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un elastomere thermoplastique et d'une charge lamellaire. |
| FR2953449B1 (fr) | 2009-12-03 | 2011-11-18 | Michelin Soc Tech | Pneumatique comportant une armature de carcasse constituee de cables et de tubes capillaires |
| FR2954336B1 (fr) | 2009-12-23 | 2013-01-04 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un elastomere thermoplastique styrenique et d'un polyphenylene ether |
| FR2954334B1 (fr) | 2009-12-23 | 2013-01-25 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un melange d'un elastomere thermoplastique et d'un caoutchouc butyl |
| FR2954335B1 (fr) | 2009-12-23 | 2013-01-11 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un melange d'un elastomere thermoplastique et d'un caoutchouc butyl partiellement reticule |
| FR2959234B1 (fr) | 2010-04-21 | 2013-09-27 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un elastomere thermoplastique et d'une resine hydrocarbonee. |
| FR2959963B1 (fr) | 2010-05-12 | 2015-04-24 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un elastomere thermoplastique et d'un thermoplastique |
| FR2962368B1 (fr) | 2010-07-09 | 2012-08-31 | Michelin Soc Tech | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un melange d'un caoutchouc butyl et d'un elastomere thermoplastique |
| KR101459120B1 (ko) | 2010-12-31 | 2014-11-12 | 제일모직주식회사 | 내마모성이 우수한 저경도 고강도 열가소성 고무 및 이를 포함하는 다이아프램 |
| TWI453224B (zh) | 2010-12-31 | 2014-09-21 | Chi Mei Corp | 末端改質的共軛二烯－乙烯基芳香烴共聚物及其製備方法 |
| US9156985B2 (en) * | 2011-04-06 | 2015-10-13 | Nok Corporation | Fluororubber composition |
| EP2714798B1 (en) | 2011-05-31 | 2016-04-13 | PolyOne Corporation | Thermoplastic elastomer compounds exhibiting superior compression set properties |
| DE112012003530B4 (de) * | 2011-08-26 | 2017-03-02 | The Yokohama Rubber Co., Ltd. | Kautschukzusammensetzung für Reifenlaufflächen sowie deren Verwendung |
| KR101482027B1 (ko) * | 2011-12-15 | 2015-01-21 | 제일모직주식회사 | 저경도 열가소성 고무 조성물 및 이를 포함하는 다이아프램 |
| FR2984339B1 (fr) | 2011-12-16 | 2018-01-12 | Soc Tech Michelin | Pneumatique pourvu d'une bande de roulement a base d'un melange d'un elastomere dienique et d'un elastomere thermoplastique |
| FR2984335B1 (fr) | 2011-12-16 | 2018-01-12 | Societe De Technologie Michelin | Pneumatique pourvu d'une couche interne a base d'un melange d'un elastomere dienique et d'un elastomere thermoplastique |
| FR2984340B1 (fr) | 2011-12-16 | 2018-01-12 | Soc Tech Michelin | Pneumatique pourvu d'un flanc externe a base d'un melange d'un elastomere dienique et d'un elastomere thermoplastique |
| FR2990157B1 (fr) | 2012-05-03 | 2014-04-25 | Michelin & Cie | Objet pneumatique pourvu d'une couche etanche aux gaz a base d'un elastomere thermoplastique et d'une charge lamellaire |
| FR2993817B1 (fr) | 2012-07-30 | 2014-08-08 | Michelin & Cie | Stratifie multicouche pour pneumatique |
| US9251927B2 (en) * | 2012-08-13 | 2016-02-02 | Joinset Co., Ltd. | Cable having reduced tangle ability |
| US20160031190A1 (en) | 2013-03-05 | 2016-02-04 | Compagnie Generale Des Etablissements Michelin | Elastomeric laminate for a tire |
| FR3049029B1 (fr) | 2016-03-18 | 2018-03-09 | Hutchinson | Dispositif antivibratoire tenant au feu destine a une application ferroviaire |
| CN106589632B (zh) * | 2016-12-02 | 2018-12-28 | 新疆天利高新石化股份有限公司 | 一种微交联热塑性弹性体密封材料及其制备方法 |
| DE102017222256A1 (de) * | 2017-12-08 | 2019-06-13 | Bayerische Motoren Werke Aktiengesellschaft | Kraftstofftank für ein Kraftfahrzeug, insbesondere für ein Motorrad, sowie Verfahren zum Herstellen eines Kraftstofftanks |
| WO2021231362A1 (en) | 2020-05-12 | 2021-11-18 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomer compositions for use in pharmaceutical articles |
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| US5672660A (en) | 1995-12-01 | 1997-09-30 | Advanced Elastomer Systems, L.P. | Hydrosilylation crosslinking |
| JP3545548B2 (ja) * | 1996-10-03 | 2004-07-21 | 鐘淵化学工業株式会社 | 熱可塑性樹脂組成物 |
| CA2221974A1 (en) * | 1996-11-25 | 1998-05-25 | Kaneka Corporation | Curable composition |
| JP3583593B2 (ja) | 1997-09-29 | 2004-11-04 | 鐘淵化学工業株式会社 | 架橋可能なゴム組成物、及びその架橋ゴム |
| JP3540920B2 (ja) * | 1997-09-29 | 2004-07-07 | 鐘淵化学工業株式会社 | 架橋可能なゴム組成物、及びその架橋ゴム |
| JP3941988B2 (ja) * | 1997-12-04 | 2007-07-11 | 株式会社カネカ | アルケニル基含有イソブチレン系ブロック共重合体及びその製造方法 |
| JP2001316483A (ja) * | 2000-05-02 | 2001-11-13 | Advanced Elastomer Syst Lp | オルガノシランで硬化されたブチルゴム／ポリプロピレン熱可塑性加硫ゴム |
| TWI300425B (en) | 2001-06-28 | 2008-09-01 | Kaneka Corp | Thermoplastic elastomer composition |
-
2003
- 2003-10-16 MX MXPA05004529A patent/MXPA05004529A/es active IP Right Grant
- 2003-10-16 CA CA002503805A patent/CA2503805A1/en not_active Abandoned
- 2003-10-16 AU AU2003273031A patent/AU2003273031A1/en not_active Abandoned
- 2003-10-16 WO PCT/JP2003/013274 patent/WO2004044050A1/ja not_active Ceased
- 2003-10-16 AT AT03754161T patent/ATE451424T1/de not_active IP Right Cessation
- 2003-10-16 EP EP03754161A patent/EP1561783B1/en not_active Expired - Lifetime
- 2003-10-16 DE DE60330491T patent/DE60330491D1/de not_active Expired - Lifetime
- 2003-10-16 BR BR0315641-9A patent/BR0315641A/pt not_active IP Right Cessation
- 2003-10-16 US US10/532,893 patent/US7105611B2/en not_active Expired - Fee Related
- 2003-10-21 TW TW092129172A patent/TW200420651A/zh not_active IP Right Cessation
- 2003-10-23 MY MYPI20034045A patent/MY135496A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MY135496A (en) | 2008-04-30 |
| US7105611B2 (en) | 2006-09-12 |
| ATE451424T1 (de) | 2009-12-15 |
| CA2503805A1 (en) | 2004-05-27 |
| AU2003273031A1 (en) | 2004-06-03 |
| TW200420651A (en) | 2004-10-16 |
| DE60330491D1 (de) | 2010-01-21 |
| MXPA05004529A (es) | 2005-07-26 |
| EP1561783B1 (en) | 2009-12-09 |
| EP1561783A1 (en) | 2005-08-10 |
| US20060004144A1 (en) | 2006-01-05 |
| EP1561783A4 (en) | 2006-08-23 |
| WO2004044050A1 (ja) | 2004-05-27 |
| BR0315641A (pt) | 2005-08-30 |
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| MM4A | Annulment or lapse of patent due to non-payment of fees |