JP3436935B2 - 結合非対称ポリマーの製造方法 - Google Patents
結合非対称ポリマーの製造方法Info
- Publication number
- JP3436935B2 JP3436935B2 JP50847195A JP50847195A JP3436935B2 JP 3436935 B2 JP3436935 B2 JP 3436935B2 JP 50847195 A JP50847195 A JP 50847195A JP 50847195 A JP50847195 A JP 50847195A JP 3436935 B2 JP3436935 B2 JP 3436935B2
- Authority
- JP
- Japan
- Prior art keywords
- vinyl aromatic
- aromatic hydrocarbon
- molecular weight
- block
- asymmetric
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920000642 polymer Polymers 0.000 title claims description 88
- 238000004519 manufacturing process Methods 0.000 title abstract description 8
- -1 vinyl aromatic hydrocarbon Chemical class 0.000 claims abstract description 59
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 51
- 239000007822 coupling agent Substances 0.000 claims abstract description 35
- 229920001400 block copolymer Polymers 0.000 claims abstract description 28
- 239000000178 monomer Substances 0.000 claims abstract description 22
- 150000001993 dienes Chemical class 0.000 claims abstract description 20
- 239000003505 polymerization initiator Substances 0.000 claims abstract description 18
- 238000010539 anionic addition polymerization reaction Methods 0.000 claims abstract description 9
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 26
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 20
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 11
- 238000005227 gel permeation chromatography Methods 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 abstract description 16
- 238000010168 coupling process Methods 0.000 abstract description 9
- 238000005859 coupling reaction Methods 0.000 abstract description 9
- 230000008878 coupling Effects 0.000 abstract description 8
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 13
- 239000004793 Polystyrene Substances 0.000 description 13
- 229920002223 polystyrene Polymers 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 8
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000000149 argon plasma sintering Methods 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000009826 distribution Methods 0.000 description 5
- 125000000524 functional group Chemical group 0.000 description 5
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229920006216 polyvinyl aromatic Polymers 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000009739 binding Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 229920002959 polymer blend Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000005049 silicon tetrachloride Substances 0.000 description 2
- 150000003440 styrenes Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- DQFAIOJURQGXBT-UHFFFAOYSA-N 1,2,4-tris(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C(C=C)=C1 DQFAIOJURQGXBT-UHFFFAOYSA-N 0.000 description 1
- MPGOMZYTJXESSF-UHFFFAOYSA-N 1,2,5-tris(ethenyl)-3,7-diethylnaphthalene Chemical compound C1=C(CC)C(C=C)=C(C=C)C2=CC(CC)=CC(C=C)=C21 MPGOMZYTJXESSF-UHFFFAOYSA-N 0.000 description 1
- ZJQIXGGEADDPQB-UHFFFAOYSA-N 1,2-bis(ethenyl)-3,4-dimethylbenzene Chemical compound CC1=CC=C(C=C)C(C=C)=C1C ZJQIXGGEADDPQB-UHFFFAOYSA-N 0.000 description 1
- FWFAJEYKHANIJP-UHFFFAOYSA-N 1,3,5-tris(ethenyl)naphthalene Chemical compound C1=CC=C(C=C)C2=CC(C=C)=CC(C=C)=C21 FWFAJEYKHANIJP-UHFFFAOYSA-N 0.000 description 1
- SZEZDFQBIICMNO-UHFFFAOYSA-N 1,3-bis(ethenyl)-5-(4-ethenylphenyl)benzene Chemical group C1=CC(C=C)=CC=C1C1=CC(C=C)=CC(C=C)=C1 SZEZDFQBIICMNO-UHFFFAOYSA-N 0.000 description 1
- PRJNEUBECVAVAG-UHFFFAOYSA-N 1,3-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1 PRJNEUBECVAVAG-UHFFFAOYSA-N 0.000 description 1
- TUDTVAXRTPHZAJ-UHFFFAOYSA-N 1,3-bis(ethenyl)naphthalene Chemical compound C1=CC=CC2=CC(C=C)=CC(C=C)=C21 TUDTVAXRTPHZAJ-UHFFFAOYSA-N 0.000 description 1
- WEERVPDNCOGWJF-UHFFFAOYSA-N 1,4-bis(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C=C1 WEERVPDNCOGWJF-UHFFFAOYSA-N 0.000 description 1
- HFOCWQKBVRVPGX-UHFFFAOYSA-N 1,7,8-tributyl-2,4-bis(ethenyl)naphthalene Chemical compound C=CC1=CC(C=C)=C(CCCC)C2=C(CCCC)C(CCCC)=CC=C21 HFOCWQKBVRVPGX-UHFFFAOYSA-N 0.000 description 1
- FTUDIUREWUBVKL-UHFFFAOYSA-N 1,8-bis(ethenyl)naphthalene Chemical compound C1=CC(C=C)=C2C(C=C)=CC=CC2=C1 FTUDIUREWUBVKL-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical class C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- JVXPEVSEOVECRV-UHFFFAOYSA-N 2,4-bis(ethenyl)-1-phenylbenzene Chemical group C=CC1=CC(C=C)=CC=C1C1=CC=CC=C1 JVXPEVSEOVECRV-UHFFFAOYSA-N 0.000 description 1
- WFAQEKGVNQWFTG-UHFFFAOYSA-N 2-ethenyl-1-(2-ethenyl-4-ethylphenyl)-4-propylbenzene Chemical group C=CC1=CC(CCC)=CC=C1C1=CC=C(CC)C=C1C=C WFAQEKGVNQWFTG-UHFFFAOYSA-N 0.000 description 1
- QTTAWIGVQMSWMV-UHFFFAOYSA-N 3,4-dimethylhexa-1,3-diene Chemical compound CCC(C)=C(C)C=C QTTAWIGVQMSWMV-UHFFFAOYSA-N 0.000 description 1
- OCTVDLUSQOJZEK-UHFFFAOYSA-N 4,5-diethylocta-1,3-diene Chemical compound CCCC(CC)C(CC)=CC=C OCTVDLUSQOJZEK-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- KFGGIMLZUQHTMC-UHFFFAOYSA-N ClP1(P(P(C=CN1)(Cl)Cl)(Cl)Cl)Cl Chemical compound ClP1(P(P(C=CN1)(Cl)Cl)(Cl)Cl)Cl KFGGIMLZUQHTMC-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920001744 Polyaldehyde Polymers 0.000 description 1
- 229920002732 Polyanhydride Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000005110 aryl thio group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- KCWYOFZQRFCIIE-UHFFFAOYSA-N ethylsilane Chemical compound CC[SiH3] KCWYOFZQRFCIIE-UHFFFAOYSA-N 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 150000004820 halides Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002900 organolithium compounds Chemical class 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical class C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- GQMOTYMECCJBDG-UHFFFAOYSA-N trichloro(1-trichlorosilylethyl)silane Chemical compound Cl[Si](Cl)(Cl)C(C)[Si](Cl)(Cl)Cl GQMOTYMECCJBDG-UHFFFAOYSA-N 0.000 description 1
- CLXMTJZPFVPWAX-UHFFFAOYSA-N trichloro-[dichloro(trichlorosilyloxy)silyl]oxysilane Chemical compound Cl[Si](Cl)(Cl)O[Si](Cl)(Cl)O[Si](Cl)(Cl)Cl CLXMTJZPFVPWAX-UHFFFAOYSA-N 0.000 description 1
- PPDADIYYMSXQJK-UHFFFAOYSA-N trichlorosilicon Chemical group Cl[Si](Cl)Cl PPDADIYYMSXQJK-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000008096 xylene Substances 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
- C08F297/044—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 coupling agent
-
- 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
- C08F297/046—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 polymerising vinyl aromatic monomers and isoprene, optionally with other conjugated dienes
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compounds Of Unknown Constitution (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/120,116 US5360875A (en) | 1993-09-10 | 1993-09-10 | Method for producing coupled asymmetric polymers |
| US08/120,116 | 1993-09-10 | ||
| PCT/EP1994/003037 WO1995007307A1 (en) | 1993-09-10 | 1994-09-09 | Method for producing coupled asymmetric polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH09502217A JPH09502217A (ja) | 1997-03-04 |
| JP3436935B2 true JP3436935B2 (ja) | 2003-08-18 |
Family
ID=22388363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50847195A Expired - Lifetime JP3436935B2 (ja) | 1993-09-10 | 1994-09-09 | 結合非対称ポリマーの製造方法 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5360875A (enExample) |
| EP (1) | EP0717756B1 (enExample) |
| JP (1) | JP3436935B2 (enExample) |
| KR (1) | KR100346567B1 (enExample) |
| CN (1) | CN1066159C (enExample) |
| AT (1) | ATE164382T1 (enExample) |
| AU (1) | AU7781394A (enExample) |
| BR (1) | BR9407436A (enExample) |
| DE (1) | DE69409246T2 (enExample) |
| DK (1) | DK0717756T3 (enExample) |
| ES (1) | ES2114702T3 (enExample) |
| GR (1) | GR3026736T3 (enExample) |
| TW (1) | TW262477B (enExample) |
| WO (1) | WO1995007307A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210142385A (ko) * | 2020-05-18 | 2021-11-25 | 주식회사 엘지화학 | 블록 공중합체 조성물, 이의 제조방법 및 이를 포함하는 점착제 조성물 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5446093A (en) * | 1993-11-10 | 1995-08-29 | Shell Oil Company | Method for producing statistically coupled asymmetric radial polymers |
| US5616542A (en) * | 1996-04-03 | 1997-04-01 | Shell Oil Company | Oil with asymmetric radial polymer having block copolymer arm |
| DE60031280T2 (de) * | 1999-08-31 | 2007-01-25 | Nippon Soda Co. Ltd. | Sternblockcopolymer |
| JP4623690B2 (ja) * | 1999-08-31 | 2011-02-02 | 日本曹達株式会社 | 星型ブロックコポリマー |
| US6579940B1 (en) | 1999-10-28 | 2003-06-17 | Edwards Lifesciences Corporation | Thermoplastic elastomeric material as a replacement for natural rubber latex |
| DE60030551T2 (de) * | 2000-07-20 | 2007-06-06 | Dynasol Elastomeros, S.A. | Styrol-1,3-Butadienblockcopolymere und Wasserdichtmembranen hergestellt davon |
| US6613838B1 (en) | 2000-08-30 | 2003-09-02 | Edwards Lifesciences Corporation | Synthetic rubber elastomers as replacements for natural rubber latex |
| US8349950B2 (en) * | 2008-03-13 | 2013-01-08 | Kraton Polymers Us Llc | Miktopolymer compositions |
| US8604136B2 (en) | 2009-10-16 | 2013-12-10 | Exxonmobil Research And Engineering Company | Process for making dendritic hydrocarbon polymers |
| US20110214909A1 (en) | 2010-03-05 | 2011-09-08 | International Business Machines Corporation | Hydrophobic Silane Coating for Preventing Conductive Anodic Filament (CAF) Growth in Printed Circuit Boards |
| US8629217B2 (en) | 2011-11-22 | 2014-01-14 | Exxonmobil Chemical Patents Inc. | Modified polyethylene blown film compositions having excellent bubble stability |
| CN103254544B (zh) * | 2012-02-21 | 2015-10-21 | 中国石油化工股份有限公司 | 单乙烯基芳烃-共轭二烯烃共聚物组合物和聚合方法及由该方法制备的聚合物 |
| EP3143056B1 (en) | 2014-05-16 | 2021-01-13 | Kraton Polymers U.S. LLC | Polyalkenyl coupling agent and conjugated diene polymers prepared therefrom |
| TWI604002B (zh) * | 2015-03-09 | 2017-11-01 | 科騰聚合物美國有限責任公司 | 用於固化嵌段共聚物乳膠薄膜之改良硫化系統 |
| US10212812B2 (en) | 2016-01-15 | 2019-02-19 | International Business Machines Corporation | Composite materials including filled hollow glass filaments |
| CN109181813B (zh) * | 2018-07-31 | 2021-07-06 | 沈阳化工研究院有限公司 | 一种用于润滑油的星形黏度指数改进剂及其制备方法 |
| US11608404B2 (en) | 2020-05-22 | 2023-03-21 | Kraton Corporation | Block copolymers and polymer modified bitumen therefrom |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3639517A (en) * | 1969-09-22 | 1972-02-01 | Phillips Petroleum Co | Resinous branched block copolymers |
| US3939112A (en) * | 1974-11-18 | 1976-02-17 | Phillips Petroleum Company | Thermoplastic resin composition having high impact strength |
| US4167545A (en) * | 1975-11-08 | 1979-09-11 | Basf Aktiengesellschaft | Branched block copolymers and their manufacture |
| DE2550226C2 (de) * | 1975-11-08 | 1984-12-13 | Basf Ag, 6700 Ludwigshafen | Verzweigte Blockcopolymerisate und Verfahren zu ihrer Herstellung |
| US4080407A (en) * | 1975-11-10 | 1978-03-21 | Phillips Petroleum Company | Resinous linear copolymers having blocks with a heterogeneity index of 2.3 to 4.5 |
| US4091053A (en) * | 1976-06-24 | 1978-05-23 | Phillips Petroleum Company | Coupled resinous diene copolymer with good integral hinge flex life and high hardness |
| US4248983A (en) * | 1979-02-05 | 1981-02-03 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
| US4180530A (en) * | 1979-02-05 | 1979-12-25 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
| US4248981A (en) * | 1979-04-30 | 1981-02-03 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
| US4248982A (en) * | 1979-04-30 | 1981-02-03 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
| US4248984A (en) * | 1979-05-11 | 1981-02-03 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
| US4221884A (en) * | 1979-05-14 | 1980-09-09 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
| US4390663A (en) * | 1981-02-17 | 1983-06-28 | Atlantic Richfield Company | Semi-continuous process for making star-block copolymers |
| US4391949A (en) * | 1981-11-12 | 1983-07-05 | Shell Oil Company | Asymmetric block copolymers and corresponding adhesive formulations |
| US4788232A (en) * | 1985-03-11 | 1988-11-29 | Phillips Petroleum Company | Pigment concentrates for resins |
| US4600736A (en) * | 1985-03-11 | 1986-07-15 | Phillips Petroleum Company | Pigment concentrates for resins |
| US4720514A (en) * | 1985-03-11 | 1988-01-19 | Phillips Petroleum Company | Pigment concentrates for resins |
| DE3537772A1 (de) * | 1985-10-24 | 1987-04-30 | Basf Ag | Transparente, schlagzaehe styrol-block-polymerisate und verfahren zu ihrer herstellung |
| IT1196517B (it) * | 1986-07-17 | 1988-11-16 | Montedipe Spa | Copolimeri a blocco radiali e bimodali aventi ottime proprieta' ottiche e reistenza agli urti e processo per la loro preparazione |
| CA1335614C (en) * | 1987-10-30 | 1995-05-16 | Ronald James Hoxmeier | Method for preparing asymmetric radial copolymers |
| DE3738748A1 (de) * | 1987-11-14 | 1989-05-24 | Basf Ag | Verfahren zur diskontinuierlichen herstellung von unsymmetrisch aufgebauten, sternfoermig verzweigten blockcopolymerisaten und ihre verwendung |
| DE3833760A1 (de) * | 1988-10-05 | 1990-04-12 | Huels Chemische Werke Ag | Ungesaettigte, elastomere, asymmetrisch gekuppelte blockcopolymere, ein eintopfverfahren zu ihrer herstellung und ihre verwendung zur herstellung von reifenbauteilen |
| US5212249A (en) * | 1991-10-28 | 1993-05-18 | Shell Oil Company | Method for preparing asymmetric radial polymers |
-
1993
- 1993-09-10 US US08/120,116 patent/US5360875A/en not_active Expired - Lifetime
-
1994
- 1994-08-23 TW TW083107740A patent/TW262477B/zh active
- 1994-09-09 AT AT94928333T patent/ATE164382T1/de not_active IP Right Cessation
- 1994-09-09 CN CN94193711A patent/CN1066159C/zh not_active Expired - Lifetime
- 1994-09-09 ES ES94928333T patent/ES2114702T3/es not_active Expired - Lifetime
- 1994-09-09 DE DE69409246T patent/DE69409246T2/de not_active Expired - Lifetime
- 1994-09-09 BR BR9407436A patent/BR9407436A/pt not_active IP Right Cessation
- 1994-09-09 JP JP50847195A patent/JP3436935B2/ja not_active Expired - Lifetime
- 1994-09-09 KR KR1019960701217A patent/KR100346567B1/ko not_active Expired - Lifetime
- 1994-09-09 DK DK94928333.7T patent/DK0717756T3/da active
- 1994-09-09 WO PCT/EP1994/003037 patent/WO1995007307A1/en not_active Ceased
- 1994-09-09 AU AU77813/94A patent/AU7781394A/en not_active Abandoned
- 1994-09-09 EP EP94928333A patent/EP0717756B1/en not_active Expired - Lifetime
-
1998
- 1998-04-28 GR GR980400926T patent/GR3026736T3/el unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210142385A (ko) * | 2020-05-18 | 2021-11-25 | 주식회사 엘지화학 | 블록 공중합체 조성물, 이의 제조방법 및 이를 포함하는 점착제 조성물 |
| KR102849963B1 (ko) | 2020-05-18 | 2025-08-27 | 주식회사 엘지화학 | 블록 공중합체 조성물, 이의 제조방법 및 이를 포함하는 점착제 조성물 |
Also Published As
| Publication number | Publication date |
|---|---|
| GR3026736T3 (en) | 1998-07-31 |
| DE69409246T2 (de) | 1998-07-23 |
| EP0717756B1 (en) | 1998-03-25 |
| ES2114702T3 (es) | 1998-06-01 |
| DK0717756T3 (da) | 1998-05-11 |
| ATE164382T1 (de) | 1998-04-15 |
| EP0717756A1 (en) | 1996-06-26 |
| WO1995007307A1 (en) | 1995-03-16 |
| JPH09502217A (ja) | 1997-03-04 |
| DE69409246D1 (de) | 1998-04-30 |
| CN1133052A (zh) | 1996-10-09 |
| CN1066159C (zh) | 2001-05-23 |
| AU7781394A (en) | 1995-03-27 |
| BR9407436A (pt) | 1996-04-09 |
| KR100346567B1 (ko) | 2002-11-30 |
| TW262477B (enExample) | 1995-11-11 |
| US5360875A (en) | 1994-11-01 |
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