KR20010032077A - 수소첨가 블록 공중합체 - Google Patents
수소첨가 블록 공중합체 Download PDFInfo
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- KR20010032077A KR20010032077A KR1020007005200A KR20007005200A KR20010032077A KR 20010032077 A KR20010032077 A KR 20010032077A KR 1020007005200 A KR1020007005200 A KR 1020007005200A KR 20007005200 A KR20007005200 A KR 20007005200A KR 20010032077 A KR20010032077 A KR 20010032077A
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- South Korea
- Prior art keywords
- block copolymer
- weight
- hydrogenated
- hydrogenated block
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- 229920001400 block copolymer Polymers 0.000 title claims abstract description 74
- 229920000642 polymer Polymers 0.000 claims abstract description 45
- -1 polypropylene Polymers 0.000 claims abstract description 35
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000004743 Polypropylene Substances 0.000 claims abstract description 23
- 229920001155 polypropylene Polymers 0.000 claims abstract description 23
- 229920005989 resin Polymers 0.000 claims abstract description 21
- 239000011347 resin Substances 0.000 claims abstract description 21
- 239000011342 resin composition Substances 0.000 claims abstract description 20
- 238000002425 crystallisation Methods 0.000 claims abstract description 19
- 230000008025 crystallization Effects 0.000 claims abstract description 19
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 19
- 150000002430 hydrocarbons Chemical group 0.000 claims abstract description 8
- 239000000178 monomer Substances 0.000 claims description 19
- 229920002554 vinyl polymer Polymers 0.000 claims description 9
- 238000011156 evaluation Methods 0.000 claims 1
- 229920005629 polypropylene homopolymer Polymers 0.000 abstract description 10
- 229920001577 copolymer Polymers 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 description 27
- 230000000903 blocking effect Effects 0.000 description 20
- 230000002087 whitening effect Effects 0.000 description 16
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 11
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 238000005481 NMR spectroscopy Methods 0.000 description 8
- 239000005062 Polybutadiene Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000008188 pellet Substances 0.000 description 6
- 229920002857 polybutadiene Polymers 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 229920005604 random copolymer Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000002981 blocking agent Substances 0.000 description 2
- 238000012661 block copolymerization Methods 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229920005673 polypropylene based resin Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 1
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 150000002642 lithium compounds Chemical class 0.000 description 1
- 238000010551 living anionic polymerization reaction Methods 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- ZWYDDDAMNQQZHD-UHFFFAOYSA-L titanium(ii) chloride Chemical compound [Cl-].[Cl-].[Ti+2] ZWYDDDAMNQQZHD-UHFFFAOYSA-L 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
- C08F297/04—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes
- C08F297/042—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes using a polyfunctional initiator
-
- 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
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
- C08F297/04—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/04—Reduction, e.g. hydrogenation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- 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
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- 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
- C08L53/025—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 modified
-
- 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
- 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
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
구조 | 1 개의 말단중합체 블록B1 의 양 (wt%) | 수소첨가율 | 스티렌양 (wt%) | MFR(g/10분) | 1,2결합량(몰%) | △Tc(℃) | |
SEBS 1 | B1-A-B2-A | 4.8 | 99.7 | 14.1 | 3.0 | 73.1 | 3.4 |
SEBS 2 | B1-A-B2-A | 11.2 | 99.7 | 14.8 | 2.8 | 73.2 | 3.5 |
SEBS 3 | B1-A-B2-A | 4.8 | 99.8 | 14.3 | 3.0 | 34.0 | 0.1 |
SEBS 4 | B1-A-B2-A | 4.8 | 99.8 | 35.0 | 3.1 | 72.0 | 2.4 |
SEBS 5 | A-B2-A | 0 | 99.7 | 9.2 | 14.1 | 72.3 | 3.7 |
SEBS 6 | A-B2-A | 0 | 99.8 | 12.1 | 6.0 | 76.5 | 3.4 |
SEBS 7 | B1-A-B2-A | 4.8 | 99.7 | 14.9 | 3.1 | 63.0 | 1.4 |
실시예1 | 비교예1 | 비교예2 | 비교예3 | 비교예4 | 비교예5 | 실시예2 | 비교예6 | ||
배합 | (1)폴리프로필렌계 수지 | PC600S80중량부 | PC600S80중량부 | PC600S80중량부 | PC600S80중량부 | PC600S80중량부 | PC600S80중량부 | FG46480중량부 | FG46480중량부 |
(2)수소첨가블록공중합체 | SEBS 120중량부 | SEBS 220중량부 | SEBS 320중량부 | SEBS 420중량부 | SEBS 620중량부 | SEBS 720중량부 | SEBS 120중량부 | SEBS 520중량부 | |
물성 | 영율 (MD)(kg/㎠) | 4000 | 4400 | 5000 | 7000 | 4800 | 4500 | 3500 | 3500 |
응력백화성(%) | 4.8 | 5.2 | 33.3 | 19.0 | 16.0 | 14.0 | 1.0 | 1.1 | |
혼탁도 (%) | 4.8 | 6.3 | 16.9 | 19.5 | 13.0 | 9.0 | 2.3 | 2.5 | |
필름 블로킹성(g/43mm) | 5 | 25 | 8 | 5 | 8 | 6 | 9 | 40 |
Claims (9)
- 비닐방향족 탄화수소 화합물 단량체 단위를 주체로 하는 2 개 이상의 중합체 블록 A 와, 수소첨가된 부타디엔 단량체 단위를 주체로 하는 2 개 이상의 중합체 블록 B 로 구성되고, 수소첨가되기 전의 부타디엔 단량체 단위를 주체로 하는 중합체 블록 중의 올레핀성 불포화 이중 결합 중, 90% 이상이 수소첨가된 수소첨가 블록 공중합체에 있어서, 말단에 있는 블록 중, 1 개 이상이 중합체 블록 B 이고, 또한 말단에 있는 중합체 블록 B 는 각각 수소첨가 블록 공중합체 중에서 차지하는 비율이 0.1 중량% 이상 9.1 중량% 미만이고, 수소첨가 블록 공중합체에 있어서 비닐방향족 탄화수소 화합물이 수소첨가 블록 공중합체 중에서 차지하는 비율이 10 중량% 초과 25 중량% 미만이고, 수소첨가 전의 부타디엔 단량체 단위를 주체로 하는 중합체 블록의 1,2 결합량의 평균이 62 몰% 이상 99 몰% 미만이고, 동일배열(isotactic) 호모폴리프로필렌의 결정화 개시 온도 (Tc1) 와 상기 수소첨가 블록 공중합체를 첨가한 경우의 결정화 개시 온도 (Tc2) 의 차 △Tc (Tc1-Tc2) 가 1.5℃ 이상인 것을 특징으로 하는 수소첨가 블록 공중합체.
- 제 1 항에 있어서, 비닐방향족 탄화수소 화합물이 수소첨가 블록 공중합체 중에서 차지하는 비율이 12 중량% 이상 25 중량% 미만인 수소첨가 블록 공중합체.
- 제 1 항에 있어서, △Tc (Tc1-Tc2) 가 2.0℃ 이상인 수소첨가 블록 공중합체.
- 제 1 항에 있어서, 말단에 있는 중합체 블록 B 가 수소첨가 블록 공중합체 중에서 차지하는 비율이 0.5 중량% 초과 5.0 중량% 미만인 수소첨가 블록 공중합체.
- 하기 성분 (1) 및 (2) 로 이루어지는 수지 조성물:(1) 폴리프로필렌계 수지 5 내지 99 중량부,(2) 제 1 항에 기재된 수소첨가 블록 공중합체 1 내지 95 중량부.
- 제 5 항에 있어서, 성분 (2) 에서 비닐방향족 탄화수소 화합물이 수소첨가 블록 공중합체 중에서 차지하는 비율이 12 중량% 이상 25 중량% 미만인 수지 조성물.
- 제 5 항에 있어서, 성분 (2) 에서 △Tc (Tc1-Tc2) 가 2.0℃ 이상인 수지 조성물.
- 제 5 항에 있어서, 성분 (2) 에서 말단에 있는 중합체 블록 B 가 수소첨가 블록 공중합체 중에서 차지하는 비율이 0.5 중량% 초과 5.0 중량% 미만인 수지 조성물.
- 제 5 항에 기재된 수지 조성물로 이루어지는 시트 및 필름.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP98-259667 | 1998-09-14 | ||
JP25966798 | 1998-09-14 | ||
PCT/JP1999/004988 WO2000015681A1 (en) | 1998-09-14 | 1999-09-13 | Hydrogenated block copolymer |
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Publication Number | Publication Date |
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KR20010032077A true KR20010032077A (ko) | 2001-04-16 |
KR100349959B1 KR100349959B1 (ko) | 2002-08-24 |
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Application Number | Title | Priority Date | Filing Date |
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KR1020007005200A KR100349959B1 (ko) | 1998-09-14 | 1999-09-13 | 수소첨가 블록 공중합체 |
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US (1) | US6455635B1 (ko) |
EP (1) | EP1031586B1 (ko) |
JP (1) | JP4902047B2 (ko) |
KR (1) | KR100349959B1 (ko) |
TW (1) | TW483902B (ko) |
WO (1) | WO2000015681A1 (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100554292B1 (ko) * | 2002-11-08 | 2006-02-24 | 금호석유화학 주식회사 | 가공성이 우수하고 경도 조절이 용이한 수첨된 스티렌계블록공중합체 수지조성물 및 그 성형품 |
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JP3938270B2 (ja) * | 2000-06-29 | 2007-06-27 | 三菱電機株式会社 | 光中継増幅装置 |
EP1258498B1 (en) * | 2000-10-25 | 2014-04-02 | Asahi Kasei Kabushiki Kaisha | Hydrogenated polymer |
JP3723472B2 (ja) | 2000-10-31 | 2005-12-07 | 三ツ星ベルト株式会社 | スラッシュ成形用熱可塑性エラストマー組成物、粉末物およびこれを用いた表皮体 |
CN100347205C (zh) * | 2001-04-11 | 2007-11-07 | 旭化成株式会社 | 氢化聚合物及其生产方法 |
EP1492830B1 (en) * | 2002-03-28 | 2010-01-06 | Kraton Polymers Research B.V. | Novel tetrablock copolymer and compositions containing same |
US7439301B2 (en) | 2004-03-03 | 2008-10-21 | Kraton Polymers U.S. Llc | Block copolymers having high flow and high elasticity |
EP2058345B1 (en) * | 2006-08-16 | 2013-02-20 | Asahi Kasei Chemicals Corporation | Process for producing block copolymer, and block copolymer or hydrogenated product thereof |
WO2009151029A1 (ja) * | 2008-06-09 | 2009-12-17 | Jsr株式会社 | 封止材料およびそれを用いた太陽電池モジュール |
ES2543189T3 (es) | 2011-05-27 | 2015-08-17 | Asahi Kasei Chemicals Corporation | Método para producir un copolímero de dieno conjugado hidrogenado |
TWI495670B (zh) | 2012-06-26 | 2015-08-11 | Asahi Kasei Chemicals Corp | Hydrogenated block copolymer pellets, polyolefin resin compositions and shaped articles thereof |
JP2014034625A (ja) * | 2012-08-08 | 2014-02-24 | Asahi Kasei Chemicals Corp | 水添ブロック共重合体、ポリオレフィン系樹脂組成物、及びその成形体 |
WO2016002764A1 (ja) | 2014-07-01 | 2016-01-07 | 旭化成ケミカルズ株式会社 | ポリオレフィン系樹脂組成物、フィルム、医療用バッグ及びチューブ |
TWI612067B (zh) | 2015-08-24 | 2018-01-21 | Asahi Chemical Ind | 氫化嵌段共聚物與使用其之聚丙烯系樹脂組合物及其成型體 |
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US4386125A (en) * | 1981-02-20 | 1983-05-31 | Asahi Kasei Kogyo Kabushiki Kaisha | Film, sheet or tube of a block copolymer or a composition containing the same |
JPH0615649B2 (ja) * | 1984-07-26 | 1994-03-02 | 旭化成工業株式会社 | 水素添加したブロツク共重合体組成物 |
EP0173380A1 (en) * | 1984-08-31 | 1986-03-05 | Shell Internationale Researchmaatschappij B.V. | Modified block copolymers and processes for the preparation therefore. |
EP0263678B1 (en) | 1986-10-07 | 1992-01-15 | Mitsubishi Petrochemical Co., Ltd. | Polyphenylene ether composition |
US5189110A (en) | 1988-12-23 | 1993-02-23 | Asahi Kasei Kogyo Kabushiki Kaisha | Shape memory polymer resin, composition and the shape memorizing molded product thereof |
CA2056206C (en) * | 1990-11-29 | 1996-02-06 | Norio Onofusa | Cover for accomodating air bag in air bag system |
JP3555257B2 (ja) | 1995-06-29 | 2004-08-18 | 旭化成ケミカルズ株式会社 | 樹脂組成物 |
DE69613405T2 (de) | 1996-02-27 | 2002-05-02 | Asahi Kasei Kabushiki Kaisha, Osaka | Überzug für airbagvorrichtung mit einer thermoplastischen elastomerzusammensetzung |
DE19815895C2 (de) | 1997-04-09 | 2000-04-13 | Asahi Chemical Ind | Hydrierte Blockcopolymere, diese enthaltende Zusammensetzungen und Formkörper |
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1999
- 1999-09-13 WO PCT/JP1999/004988 patent/WO2000015681A1/ja active IP Right Grant
- 1999-09-13 US US09/554,310 patent/US6455635B1/en not_active Expired - Lifetime
- 1999-09-13 JP JP2000570218A patent/JP4902047B2/ja not_active Expired - Lifetime
- 1999-09-13 EP EP99943311.3A patent/EP1031586B1/en not_active Expired - Lifetime
- 1999-09-13 KR KR1020007005200A patent/KR100349959B1/ko active IP Right Grant
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KR100554292B1 (ko) * | 2002-11-08 | 2006-02-24 | 금호석유화학 주식회사 | 가공성이 우수하고 경도 조절이 용이한 수첨된 스티렌계블록공중합체 수지조성물 및 그 성형품 |
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EP1031586A1 (en) | 2000-08-30 |
WO2000015681A1 (en) | 2000-03-23 |
JP4902047B2 (ja) | 2012-03-21 |
US6455635B1 (en) | 2002-09-24 |
KR100349959B1 (ko) | 2002-08-24 |
TW483902B (en) | 2002-04-21 |
EP1031586A4 (en) | 2001-06-27 |
EP1031586B1 (en) | 2018-12-26 |
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