KR910014417A - 테이퍼된 블록 공중합체의 제조방법 - Google Patents

테이퍼된 블록 공중합체의 제조방법 Download PDF

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KR910014417A
KR910014417A KR1019900020906A KR900020906A KR910014417A KR 910014417 A KR910014417 A KR 910014417A KR 1019900020906 A KR1019900020906 A KR 1019900020906A KR 900020906 A KR900020906 A KR 900020906A KR 910014417 A KR910014417 A KR 910014417A
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monovinyl aromatic
aromatic monomer
weight percent
monomer
filled
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KR0133058B1 (ko
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제임즈 트레프카 윌리엄
앤소니 목지젬버 조오지
코울맨 파라 쥬니어 랠프
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제이 이이 휘립프스
휘립프스 피트로오리암 캄파니
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/02Macromolecular 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
    • C08F297/04Macromolecular 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F297/00Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
    • C08F297/02Macromolecular 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
    • C08F297/04Macromolecular 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
    • C08F297/044Macromolecular 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2325/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • C08J2325/08Copolymers of styrene
    • C08J2325/10Copolymers of styrene with conjugated dienes

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Manufacturing & Machinery (AREA)
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  • Inorganic Chemistry (AREA)
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  • Graft Or Block Polymers (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

내용 없음

Description

테이퍼된 블록 공중합체의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (14)

  1. (1)모노비닐 방향족 단량체, 랜더마이저(randomizer)및 개시제를 충전시키고, 필수적으로 완전한 중합이 일어나도록 한 후, 임의의 순서로, (2a)부가적인 모노비닐 방향족 단량체 및 개시제를 충전시키고, 필수적으로 완전한 중합이 일어나도록 하는 단계, (2b)모노비닐 방향족 단량체 및 공역 디엔 단량체의 혼합물을 충전시키고, 필수적으로 완전한 중합이 일어나도록 하는 단계, (2c)부가적인 모노비닐 방향족 단량체 및 부가적인 개시제를 충전시키고, 필수적으로 완전한 중합이 일어나도록 하는 단계를 수행시키고 난후 (3)공역 단량체를 충전시키고, 필수적으로 완전한 중합이 일어나도록 하고 마지막으로 (4)커플링제를 첨가시키는 것으로 구성된 중합체의 제조방법.
  2. 제1항에 있어서, 단계(2b)를 단계(2a)후에 수행시키고, 단계(2c)를 단계(2d)후에 수행시키는 방법.
  3. 제1항에 있어서, 상기 모노비닐 방향족 단량체가 C8-C12를 함유하고 상기 공역 디엔은 C4-C6을 함유하며, 상기 단량체를 약 60-87%모노비닐 방향족 단량체 및 13-40중량%공역 디엔 단량체의 비율로 첨가시킴으로써, 수지성 테이퍼된 블록 공중합체를 얻는 방법.
  4. 제1항에 있어서, 상기 충전물(1)의 중합이 완결된 후 그리고 충전물(3) 공역 디엔을 첨가시키기 전 마지막 충전전에 부가적인 공역 디엔을 충전시키는 것을 포함하는 방법.
  5. 제1항에 있어서, (1),(2a)및(2c)의 개시제 첨가가 공정의 경과 동안 유일한 개시제 첨가를 나타내는 방법.
  6. 제1항 내지 제5항중 어느 한 항에 있어서, 단계(2b)내의 상기 모노비닐 방향족 단량체 및 상기 공역 디엔 단량체의 중량 비율이 약 1:0.7-1:1.4의 범위내, 바람직하게 1대 1인 방법.
  7. 제1항 내지 제5항중 어느 한 항에 있어서, 단계(1)내에 충전된 상기 모노비닐 방향족 단량체가 상기 방법내에 충전된 모노 비닐 방향족 단량체의 총 중량%의 약 35-약 60중량%, 바람직하게 약 38-약 55중량%및 가장 바라직하게 약 42-약 50중량%인 방법.
  8. 제1항 내지 제5항중 어느 한 항에 있어서, 단계(2a)내에 충전된 상기 모노비닐 방향족 단량체가 상기 방법내에 충전된 모노비닐 방향족 단량체의 총 중량%의 약 10-약 35중량%인 방법.
  9. 제8항에 있어서, 단계(2a) 내에 충전된 상기 모노비닐 방향족 단량체가 상기 방법내에 충전된 모노비닐 방향족 단량체의 총 중량%의 약 15-약 29중량%, 바람직하게 약 19-약 23%인 방법.
  10. 제1항 내지 제5항중 어느 한 항에 있어서, 단계(2b)내에 충전된 상기 모노비닐 방향족 단량체가 상기 방법내에 충전된 모노비닐 방향족 단량체의 총 중량%의 약 4-약 15중량%(예컨대, 약 5-약 14중량% 또는 약 7-약 13중량%)인 방법.
  11. 제1항 내지 제5항중 어느 한 항에 있어서, 단계(2c)내에 충전된 상기 모노비닐 방향족 단량체가 상기 방법내에 충전된 모노 비닐 방향족 단량체의 총 중량%의 약 10-약 40중량%, 바람직하게 약 12-약 36중량%, 가장 바람직하게 약 15-약 31중량%인 방법.
  12. 제1항 내지 제5항중 어느 한 항에 있어서, 상기 공역 디엔 단량체가 1,3-부다디엔이고, 상기 모노비닐 방향족 단량체는 스티렌이고, 상기 유기 모노 알카리 금속 개시제는 n-부틸리튬이고, 상기 랜더마이저가 테트라히드로푸란인 방법.
  13. 제1항 내지 제5항중 어느 한 항에 있어서, 상기 커플링제가 에폭시화된 대두유이고 중합을 실질적으로 산소 및 물의 존재하지 않은 가운데 탄화수소 희석제내, 온도 -10℃-150℃에서 수행시키고, 상기 커플링제를 상기 중합 생성물과 반응 시킨 후, 계를 종결제 이어서 안정제로 처리시키고, 계속해서 임의의 남아 있는 탄화수소 희석제를 증발 분리시키는 방법.
  14. 제13항에 있어서, 상기 종결제가 물 및 이산화탄소 이고 상기 안정제가 봉쇄된 페놀 또는 유기포스파이트이고, 원한다며, 계를 종결제로 처리시킨 후 그리고 안정제로 처리시키기 전에 산화제로 처리시키는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019900020906A 1990-01-02 1990-12-18 테이퍼된 블록 공중합체의 제조방법 KR0133058B1 (ko)

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US (1) US5130377A (ko)
EP (1) EP0436225B1 (ko)
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KR (1) KR0133058B1 (ko)
AT (1) ATE124059T1 (ko)
CA (1) CA2028410C (ko)
DE (1) DE69020324T2 (ko)
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KR100471716B1 (ko) * 2002-08-03 2005-03-10 금호석유화학 주식회사 연속식 음이온 중합에 의한 내충격 비닐 방향족 고분자의제조방법

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MX23938A (es) 1994-03-31
EP0436225A1 (en) 1991-07-10
CA2028410A1 (en) 1991-07-03
ES2073503T3 (es) 1995-08-16
US5130377A (en) 1992-07-14
CA2028410C (en) 1996-09-17
ATE124059T1 (de) 1995-07-15
EP0436225B1 (en) 1995-06-21
KR0133058B1 (ko) 1998-04-13
JP2641627B2 (ja) 1997-08-20

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