KR930000557A - 선형 중합체 제조 방법 - Google Patents
선형 중합체 제조 방법 Download PDFInfo
- Publication number
- KR930000557A KR930000557A KR1019920009406A KR920009406A KR930000557A KR 930000557 A KR930000557 A KR 930000557A KR 1019920009406 A KR1019920009406 A KR 1019920009406A KR 920009406 A KR920009406 A KR 920009406A KR 930000557 A KR930000557 A KR 930000557A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- group
- range
- aromatic
- phenylphosphonite
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims 4
- 238000004519 manufacturing process Methods 0.000 title claims 3
- 238000000034 method Methods 0.000 claims 18
- 150000001875 compounds Chemical class 0.000 claims 9
- -1 (4-methoxyphenyl) phenylphosphonite Chemical compound 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 150000001993 dienes Chemical class 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 239000003999 initiator Substances 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- 150000001491 aromatic compounds Chemical class 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 229930195733 hydrocarbon Natural products 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- HORNXRXVQWOLPJ-UHFFFAOYSA-N 3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1 HORNXRXVQWOLPJ-UHFFFAOYSA-N 0.000 claims 1
- CDOMXXVCZQOOMT-UHFFFAOYSA-N [phenoxy(phenyl)phosphoryl]oxybenzene Chemical compound C=1C=CC=CC=1OP(C=1C=CC=CC=1)(=O)OC1=CC=CC=C1 CDOMXXVCZQOOMT-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- YWHLZTFSVXCILP-UHFFFAOYSA-N bis(3-chlorophenoxy)-phenylphosphane Chemical compound ClC1=CC=CC(OP(OC=2C=C(Cl)C=CC=2)C=2C=CC=CC=2)=C1 YWHLZTFSVXCILP-UHFFFAOYSA-N 0.000 claims 1
- 239000006227 byproduct Substances 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- IMDXZWRLUZPMDH-UHFFFAOYSA-N dichlorophenylphosphine Chemical compound ClP(Cl)C1=CC=CC=C1 IMDXZWRLUZPMDH-UHFFFAOYSA-N 0.000 claims 1
- QXKPLZDCTKREIA-UHFFFAOYSA-N diphenoxy(phenyl)phosphane Chemical compound C=1C=CC=CC=1OP(C=1C=CC=CC=1)OC1=CC=CC=C1 QXKPLZDCTKREIA-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000004437 phosphorous atom Chemical group 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/42—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
- C08C19/44—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups of polymers containing metal atoms exclusively at one or both ends of the skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/48—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
- C07F9/4808—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof the acid moiety containing a substituent or structure which is considered as characteristic
- C07F9/4841—Aromatic acids or derivatives (P-C aromatic linkage)
-
- 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
- C08F8/40—Introducing phosphorus atoms or phosphorus-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Inorganic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (19)
- 유기알칼리 금속 개시제 화합물 및 적어도 탄화수소 희석제의 존재하에서 적어도 공역디엔 및/또는 모노알킬렌 방향족 화합물을 중합반응시키고, 연속해서 리빙 중합체 사슬을 하기 일반식(Ⅰ)의 화합물과 접촉시킴으로 구성되는 선형 중합체의 제조 방법 :RP(X)n(OR1)2(Ⅰ)상기 식에서 R은 인원자에 연결된 탄소 원자가 이차 또는 삼차 탄소 원자인 히드로카르빌기이고; R1은 임의적으로 치환된 히드로카르빌기이고; X는 0 또는 s 원자를 나타내며; n은 0 또는 1이다.
- 제1항에 있어서, R이 방향족 히드로카르빌기, 및 바람직하게 페닐인 방법.
- 제1 또는 2항에 있어서, R1이 방향족기, 및 바람직하게 페닐기인 방법.
- 제3항에 있어서, 방향족기 R1이 극성 치환기를 운반하는 방법.
- 제4항에 있어서, 극성 치환기는 알콕시기 또는 할로겐인 방법.
- 제1-5항 중 어느 한 항에 있어서, n이 0인 방법.
- 제1-5항 중 어느 한 항에 있어서, n이 1인 경우 x가 0원자를 나타내는 방법.
- 제1-7항 중 어느 한 항에 있어서, R 및 R1이 동시에 방향족기 및 바람직하게는 페닐기를 나타내는 방법.
- 제1-3항 중 어느 한 항에 있어서, 일반식 Ⅰ의 화합물은 디페닐 페닐포스포나이트, 버스(4-메톡시페닐) 페닐포스포나이트 및 비스(3-클로로페닐) 페닐포스포나이트로 구성된 군으로부터 선택되는 방법.
- 제1-3항 중 어느 한 항에 있어서, 일반식 Ⅰ의 화합물은 디페닐 페닐포스포네이트인 방법.
- 제1-10항 중 어느 한 항에 있어서, 일반식 Ⅰ의 화합물은 개시제의 몰당 0.3-0.7몰의 범위내의 양으로 사용되는 방법.
- 제11항에 있어서, 화합물의 양이 개시제의 몰 당 0.4-0.6몰의 범위내 및 보다 바람직하게는 0.45-0.55의 범위내인 방법.
- 제1-12항 중 어느 한 항에 있어서, 공역디엔은 1, 3-부타디엔, 이소프렌 또는 이들의 혼합물인 방법.
- 제1-12항 중 어느 한 항에 있어서, 모노알킬렌 방향족 화합물은 스티렌인 방법.
- 제1-14항 중 어느 한 항에 있어서, 탄화수소 희석제는 시클로헥산인 방법.
- 제1-15항 중 어느 한 항에 있어서, -20 내지 150℃범위내 및 바람직하게는 30 내지 90℃범위내의 온도에서 수행되는 방법.
- 화합물 버스(4-메톡시페닐) 페닐포스포나이트 및 버스(3-클로로페닐) 페닐포스포나이트.
- 실온에서 디클로로 페닐포스핀을 4-메톡시페놀 또는 3-클로로페놀의 몰 초과량과 혼합시키고, 연속해서 상기 혼합물을 180-200℃범위의 온도로 서서히 가열시키고, 원하는 생성물이 형성되도록 충분히 오랜 시간 동안 반응혼합물을 유지시키는 한편, 부산물 HCl은 반응기로부터 누출되도록 하며, 마지막으로 감압하에서 잔류물을 증류시킴으로 구성된 제17항에 청구된 화합물의 제조 방법.
- 제1-16항 중 어느 한 항에서 청구한 방법에 따라 제조된 적어도 공역 디엔 및/또는 모노 알킬렌 방향족 화합물로부터 유도된 선형 중합체.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB919111872A GB9111872D0 (en) | 1991-06-03 | 1991-06-03 | Polymer process |
GB9111872.9 | 1991-06-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR930000557A true KR930000557A (ko) | 1993-01-15 |
Family
ID=10695985
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920009406A KR930000557A (ko) | 1991-06-03 | 1992-05-30 | 선형 중합체 제조 방법 |
Country Status (12)
Country | Link |
---|---|
US (1) | US5268429A (ko) |
EP (1) | EP0517317B1 (ko) |
JP (1) | JPH05209003A (ko) |
KR (1) | KR930000557A (ko) |
CN (1) | CN1067434A (ko) |
BR (1) | BR9202096A (ko) |
DE (1) | DE69207486T2 (ko) |
ES (1) | ES2082343T3 (ko) |
GB (1) | GB9111872D0 (ko) |
MX (1) | MX9202605A (ko) |
RU (1) | RU2073691C1 (ko) |
TW (1) | TW224977B (ko) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69510477T2 (de) * | 1994-03-14 | 2000-03-16 | Studiengesellschaft Kohle Mbh | Verfahren zur Herstellung von hoch verstreuten Metall-Kolloiden und von auf einem Substrat gebundenen Metall-Clusters durch elektrochemische Reduktion von Metallsalzen |
CN1271103C (zh) | 2001-01-18 | 2006-08-23 | 克拉通聚合物研究有限公司 | 粘合剂组合物 |
JP4560998B2 (ja) | 2001-02-05 | 2010-10-13 | 味の素株式会社 | 発酵法によるl−グルタミンの製造法及びl−グルタミン生産菌 |
ES2643078T3 (es) | 2003-12-22 | 2017-11-21 | Kraton Polymers U.S. Llc | Formulaciones adhesivas de los polímeros (S-I/B)X radiales |
CN101306249B (zh) * | 2008-05-30 | 2011-09-14 | 北京中星微电子有限公司 | 动作分析装置和方法 |
CN103254231B (zh) * | 2013-06-05 | 2016-02-24 | 苏州科技学院 | 苯基亚膦酸二异丙酯化合物及其制备方法 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2726226A (en) * | 1952-11-12 | 1955-12-06 | Monsanto Chemicals | Composition comprising polystyrene, butadiene-styrene copolymer, and a phosphite ester |
US3147313A (en) * | 1959-07-13 | 1964-09-01 | Phillips Petroleum Co | Process for introducing phosphinic and thionophosphinic acid end groups on alkali terinated polymers |
US3278464A (en) * | 1961-12-08 | 1966-10-11 | Hooker Chemical Corp | Phosphonated polymers |
US3341629A (en) * | 1964-05-12 | 1967-09-12 | Weston Chemical Corp | Polyphosphites and process of making same |
US3419524A (en) * | 1965-01-04 | 1968-12-31 | Weston Chemical Corp | Polyphosphites as stabilizers for hydrocarbon polymers |
US3676393A (en) * | 1968-10-14 | 1972-07-11 | Goodyear Tire & Rubber | Polyesters stabilized by phosphorus compounds |
US3778490A (en) * | 1969-04-23 | 1973-12-11 | Phillips Petroleum Co | Polar compound adjuvants for improved block polymers prepared with primary hydrocarbyllithium initiators |
US3697620A (en) * | 1970-04-22 | 1972-10-10 | American Cyanamid Co | Vulcanizable elastomer composition containing triarylphosphine and triallylcyanurate |
US3803266A (en) * | 1972-10-30 | 1974-04-09 | Phillips Petroleum Co | Phosphorous esters as coupling agents for lithium terminated resinous polymer |
FR2251567A1 (en) * | 1973-11-19 | 1975-06-13 | Anvar | Phosphorus contg. oligomers and (co) polymers - with improved adhesion, surface activity and compatibility |
US3898209A (en) * | 1973-11-21 | 1975-08-05 | Exxon Research Engineering Co | Process for controlling rheology of C{HD 3{B {30 {0 polyolefins |
FR2367098A1 (fr) * | 1976-10-06 | 1978-05-05 | Rhone Poulenc Ind | Compositions de polystyrene ignifugees |
US4248984A (en) * | 1979-05-11 | 1981-02-03 | Arco Polymers, Inc. | Clear impact resistant thermoplastic star-block copolymers |
US4233207A (en) * | 1979-07-09 | 1980-11-11 | Ciba-Geigy Corporation | Hydrolytically stable ortho-alkylated phenyl phosphonites and stabilized compositions |
US4369260A (en) * | 1981-04-20 | 1983-01-18 | Atlantic Richfield Company | Phosphorus-containing alternating copolymers |
JPS57177012A (en) * | 1981-04-23 | 1982-10-30 | Sumitomo Chem Co Ltd | Preparation of chelate resin |
US4474914A (en) * | 1981-08-31 | 1984-10-02 | Ciba-Geigy Corporation | Ortho-alkylated phenyl phosphonites and stabilized organic compositions |
US4537932A (en) * | 1983-06-03 | 1985-08-27 | Phillips Petroleum Company | Rubbery conjugated diene polymers terminated with hydrocarbyl phosphites |
US4485833A (en) * | 1983-06-03 | 1984-12-04 | Phillips Petroleum Company | Rubbery conjugated diene polymers terminated with hydrocarbyl phosphites |
GB8326014D0 (en) * | 1983-09-28 | 1983-11-02 | Shell Int Research | Preparation of branched polymers |
US4581415A (en) * | 1983-11-03 | 1986-04-08 | Allied Corporation | Polymer-bound alkyl diarylphosphinite catalyst compositions and processes for making same |
DE3504646A1 (de) * | 1985-02-12 | 1986-08-14 | Basf Ag, 6700 Ludwigshafen | Halogenfreie, selbstverloeschende thermoplastische formmasse |
-
1991
- 1991-06-03 GB GB919111872A patent/GB9111872D0/en active Pending
-
1992
- 1992-05-12 TW TW081103682A patent/TW224977B/zh active
- 1992-05-28 US US07/889,346 patent/US5268429A/en not_active Expired - Fee Related
- 1992-05-30 KR KR1019920009406A patent/KR930000557A/ko not_active Application Discontinuation
- 1992-06-01 BR BR929202096A patent/BR9202096A/pt not_active Application Discontinuation
- 1992-06-01 CN CN92104404A patent/CN1067434A/zh active Pending
- 1992-06-01 DE DE69207486T patent/DE69207486T2/de not_active Expired - Fee Related
- 1992-06-01 RU SU925011881A patent/RU2073691C1/ru active
- 1992-06-01 MX MX9202605A patent/MX9202605A/es not_active IP Right Cessation
- 1992-06-01 EP EP92201559A patent/EP0517317B1/en not_active Expired - Lifetime
- 1992-06-01 JP JP4140548A patent/JPH05209003A/ja active Pending
- 1992-06-01 ES ES92201559T patent/ES2082343T3/es not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH05209003A (ja) | 1993-08-20 |
US5268429A (en) | 1993-12-07 |
EP0517317B1 (en) | 1996-01-10 |
MX9202605A (es) | 1992-12-01 |
EP0517317A1 (en) | 1992-12-09 |
BR9202096A (pt) | 1993-02-02 |
ES2082343T3 (es) | 1996-03-16 |
DE69207486D1 (de) | 1996-02-22 |
TW224977B (ko) | 1994-06-11 |
CN1067434A (zh) | 1992-12-30 |
GB9111872D0 (en) | 1991-07-24 |
RU2073691C1 (ru) | 1997-02-20 |
DE69207486T2 (de) | 1996-06-27 |
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WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |