KR920701264A - 중합방법 및 촉매 - Google Patents
중합방법 및 촉매Info
- Publication number
- KR920701264A KR920701264A KR1019910701430A KR910701430A KR920701264A KR 920701264 A KR920701264 A KR 920701264A KR 1019910701430 A KR1019910701430 A KR 1019910701430A KR 910701430 A KR910701430 A KR 910701430A KR 920701264 A KR920701264 A KR 920701264A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- catalyst
- magnesium
- resorcinol
- nitrogen
- Prior art date
Links
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
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/65—Pretreating the metal or compound covered by group C08F4/64 before the final contacting with the metal or compound covered by group C08F4/44
- C08F4/652—Pretreating with metals or metal-containing compounds
- C08F4/654—Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
-
- 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (35)
- a)전자 공여체의 존재하에 진행되는 마그네슘 옥시 화합물과 4가 티타늄 호합물의 반응 생성물; b)오르가루미늄 하합물; c)최소한 하나의 질소원자에 인접한 탄소원자상에 존재하는 치환체에 의해 부적당하게 장애를 받지 않는 방향족 헤테로고리 질소 화합물로 이루어진 촉매 존재하에 탄소원자의 수가 최소한 3인 α-올레핀을 지니고 있고, 평균 블록길이가 짧은 것이 특징인 엘라스토머계, 주로 입체규칙성 폴리-α-올레핀을 제조하는 방법.
- 제1항에서, 방향족 헤테로고리 질소 화합물의 질소가 효과적으로 장애를 받는 엘라스토머계, 주로 신디오탁틱 폴리프로필렌을 제조하는 방법.
- 2항에서, 질소 화합물이 2,3-디메틸퀴녹살린, 퀴날딘, 2,6-루타딘, 2,4,6-코리딘 또는 테트라메틸피라진으로 이루어진 그룹에서 선택된 방법.
- 3항에서, 4가 티타늄 할라이드가 티타늄 테트라클로라이드인 방법.
- 4항에서, 마그네슘 화합물이 MgR1R2(여기서 R1은 알콕사이드 또는 아릴옥사이드 그리고 R2는 알킬, 아릴, 알콕사이드, 아릴옥사이드 또는 할로겐)인 화합물인 방법.
- 5항에서, R1과 R2가 에톡사이드인 방법.
- 5항에서, 마그네슘 화합물이 Mg4(OCH3)6(CH3OH)10X|2(여기서, X는 레졸시놀 또는 치환된 레졸시놀 모노음이온)인 방법.
- 1항에서, 방향족 헤테로고리 질소 화합물의 각 질소가 최소한 하나의 인접한 탄소원지상에 클로로 또는 메톡시기가 존재함으로 인해 덜 장애를 받는 엘라스토머계, 주로 이소탁틱 폴리-α-올레핀을 제조하는 방법.
- 8항에서, 질소 화합물이 2,6-디클로로피리딘, 2-클로로퀴놀린, 2,4,6-트리클로로피리미딘, 2,4,5,6-테트라클로로피리미딘인 방법.
- 9항에서, 4가의 티타늄 할라이드가 티타늄 클로라이드인 방법.
- 10항에서, 마크네슘 화합물이 MgR1R2(여기서 R1은 알콕사이드, 또는 아릴옥사이드 그리고 R2는 알킬, 아릴, 알콕사이드, 아릴옥사이드 또는 할로겐)인 화합물인 방법.
- 11항에서, R1과 R2가 에톡사이드인 방법.
- 11항에서, 마그네슘 화합물이 Mg4(OCH3)6(CH3OH)10X|2(여기서, X는 레졸시놀 또는 치환된 레졸시놀 모노음이온)인 방법.
- 8항에서, α-올레핀이 프로필레인 방법.
- 8항에서, α-올레핀이 1-부텐인 방법.
- 1항에서, 방향족 헤테로고리 질소 화합물 최소한 하나의 질소가 장애를 받지 않는 엘라스토머계, 주로 이소탁틱 폴리-α-올레핀을 제조하는 방법.
- 16항에서, 질소 화합물이 피라진, 3,4,5-트리클로로피리다진, 1,3,5-트리아진, 페나진, 피리딘, 2,6-디메틸피라진, 퀴나졸린, 4,6-디클로로피리미딘, 2-피콜린, 2,3,5-트리메틸피라진, 아크리딘, 2-메틸피라진, 2,5-디메틸피라진, 2,6-디메틸피라진, 2,3-디클로로퀴녹살린, 퀴놀린, 피리다진 또는 2,4-디클로로피리미딘의 방법.
- 17항에서, 4가의 티타늄 할라이드가 티타늄 클로라이드인 방법.
- 18항에서, 마그네슘 화합물이 MgR1R2(여기서 R1은 알콕사이드 또는 아릴옥사이드 그리고 R2는 알킬, 아릴, 알콕사이드, 아릴옥사이드 또는 할로겐)인 화합물인 방법.
- 19항에, R1과 R2가 에톡사이드인 방법.
- 19항에서, 마그네슘 화합물이 Mg4(OCH3)6(CH3OH)10X|2(여기서, X는 레졸시놀 또는 치환된 레졸시놀 모노음이온)인 방법.
- 16항에서, α-올레핀이 프로피레인 방법.
- 16항에서, α-올레핀이 1-부텐인 방법.
- a)전자 공여체의 존재하에 진행되는 마그네슘 옥시 화합물과 4가 티타늄 호합물의 반응 생성물; b)오르가노알루미늄 화합물; c)최소한 하나의 질소원자에 인접한 탄소원자상에 존재하는 치환체에 의해 부적당하게 장애를 받지 않는 방향족 헤테로고리 질소 화합물로 이루어진 탄소 원자의 수가 최소한 3인 α-올레핀을 지니고 있고, 평균 블록길이가 짧은 것이 특징인 엘라스토머계, 주로 입체규칙성 폴리-α-올레핀 제조용 촉매.
- 24항에서, 4가의 티타늄 할라이드가 티타늄 테트라클로라이드인 촉매.
- 제25항에서, 마그네슘 옥시 화합물이 MgR1R2(여기서 R1은 알콕사이드 또는 아릴옥사이드 그리고 R2는 알킬, 아릴, 알콕사이드, 아릴옥사이드 또는 할로겐)인 화합물인 촉매.
- 26항에서, 질소 화합물이 2,3-디메틸퀴녹살린, 퀴날딘, 2,6-루타딘, 2,4,6-콜리딘 또는 2,4-디메틸퀴놀린인 촉매.
- 27항에서, R1과 R2가 에톡시인 촉매.
- 27항에서, 마그네슘 옥시 화합물이 Mg4(OCH3)6(CH3OH)10X2(여기서, X는 레졸시놀 또는 치환된 레졸시놀 모노음이온)인 방법.
- 26항에서, 질소 화합물이 2,6-디클로로피리딘, 2-클로로퀴놀린, 2,4,6-트리클로로피리미딘, 2-클로로-6-메톡시피리딘, 2,3-디클로로퀴녹살린 또는 2,4,5,6-테트라클로로피리미딘인 촉매.
- 30항에, R1과 R2가 에톡시인 촉매.
- 30항에서, 마그네슘 옥시 화합물이 Mg4(OCH3)6(CH3OH)10X2(여기서, X는 레졸시놀 또는 치환된 레졸시놀 모노음이온)인 촉매.
- 26항에서, 질소 화합물이 파라진, 3,4,5-트리클로로피리다진, 1,3,5-트리아진, 페나진, 피리딘, 2,6-디메틸피라진, 퀴나졸린, 4,6-디클로로피리미딘, 2-피콜린, 2,3,5-트리메틸피라진, 아크리딘, 2-메틸피라진 2,5-디메틸피라진, 2,3-디메틸피라진, 2,3-디클로로퀴녹살린, 퀴놀린, 피리다진 또는 2,4-디클로로피리미딘인 촉매.
- 33항에서, R1과 R2가 에톡시인 촉매.
- 33항에서, 마그네슘 옥시 화합물이 Mg4(OCH3)6(CH3OH)10X2(여기서, X는 레졸시놀 또는 치환된 레졸시놀 모노음이온)인 촉매.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/342,832 US5270276A (en) | 1989-04-25 | 1989-04-25 | Process for the production of elastomeric, primarily syndiotactic polypropylene and catalysts for use in said process |
US07/342832 | 1989-04-25 | ||
PCT/US1990/002036 WO1990012816A1 (en) | 1989-04-25 | 1990-04-19 | Polymerization process and catalyst |
Publications (2)
Publication Number | Publication Date |
---|---|
KR920701264A true KR920701264A (ko) | 1992-08-11 |
KR940003857B1 KR940003857B1 (ko) | 1994-05-04 |
Family
ID=23343460
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910701430A KR940003857B1 (ko) | 1989-04-25 | 1990-04-19 | 중합방법 및 촉매 |
Country Status (10)
Country | Link |
---|---|
US (1) | US5270276A (ko) |
EP (1) | EP0470171B1 (ko) |
JP (1) | JP3021037B2 (ko) |
KR (1) | KR940003857B1 (ko) |
AT (1) | ATE145925T1 (ko) |
AU (1) | AU650234B2 (ko) |
CA (1) | CA2053266C (ko) |
DE (1) | DE69029324T2 (ko) |
ES (1) | ES2097146T3 (ko) |
WO (1) | WO1990012816A1 (ko) |
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US4310439A (en) * | 1979-03-07 | 1982-01-12 | Exxon Research & Engineering Co. | Novel trialkyl aluminum cocatalyst |
DE3064564D1 (en) * | 1979-04-30 | 1983-09-22 | Shell Int Research | Olefin polymerization catalyst compositions and a process for the polymerization of olefins employing such compositions |
CA1141093A (en) * | 1979-05-17 | 1983-02-08 | Brian L. Goodall | Olefin polymerization catalyst compositions and a process for the polymerization of olefins employing such compositions |
US4255281A (en) * | 1979-07-03 | 1981-03-10 | Standard Oil Company (Indiana) | Alpha-olefin polymerization catalyst and process |
FR2460964A1 (fr) * | 1979-07-06 | 1981-01-30 | Naphtachimie Sa | Copolymeres elastomeres d'ethylene et de propylene, leur fabrication et leurs applications |
US4487845A (en) * | 1980-05-09 | 1984-12-11 | Stauffer Chemical Company | Method of enhancing stereospecificity of a catalyst system |
US4347160A (en) * | 1980-06-27 | 1982-08-31 | Stauffer Chemical Company | Titanium halide catalyst system |
US4325836A (en) * | 1980-07-18 | 1982-04-20 | Stauffer Chemical Company | Novel titanium halide containing catalyst |
US4394291A (en) * | 1981-03-04 | 1983-07-19 | Phillips Petroleum Company | Polyolefin polymerization process and catalyst |
US4442276A (en) * | 1982-02-12 | 1984-04-10 | Mitsui Petrochemical Industries, Ltd. | Process for polymerizing or copolymerizing olefins |
US4581342A (en) * | 1984-11-26 | 1986-04-08 | Standard Oil Company (Indiana) | Supported olefin polymerization catalyst |
JPH06104687B2 (ja) * | 1985-06-18 | 1994-12-21 | 東燃株式会社 | オレフイン重合用触媒 |
JPH0725807B2 (ja) * | 1985-12-20 | 1995-03-22 | 東燃株式会社 | オレフイン重合用触媒成分の製造方法 |
US4710482A (en) * | 1986-06-18 | 1987-12-01 | Shell Oil Company | Olefin polymerization catalyst component |
GB8708778D0 (en) * | 1987-04-13 | 1987-05-20 | Ici Plc | Particulate solid |
US5270276A (en) * | 1989-04-25 | 1993-12-14 | Shell Oil Company | Process for the production of elastomeric, primarily syndiotactic polypropylene and catalysts for use in said process |
-
1989
- 1989-04-25 US US07/342,832 patent/US5270276A/en not_active Expired - Fee Related
-
1990
- 1990-04-19 DE DE69029324T patent/DE69029324T2/de not_active Expired - Fee Related
- 1990-04-19 ES ES90907557T patent/ES2097146T3/es not_active Expired - Lifetime
- 1990-04-19 AT AT90907557T patent/ATE145925T1/de not_active IP Right Cessation
- 1990-04-19 KR KR1019910701430A patent/KR940003857B1/ko not_active IP Right Cessation
- 1990-04-19 WO PCT/US1990/002036 patent/WO1990012816A1/en active IP Right Grant
- 1990-04-19 EP EP90907557A patent/EP0470171B1/en not_active Expired - Lifetime
- 1990-04-19 AU AU56557/90A patent/AU650234B2/en not_active Ceased
- 1990-04-19 CA CA002053266A patent/CA2053266C/en not_active Expired - Fee Related
- 1990-04-19 JP JP2507481A patent/JP3021037B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH04504875A (ja) | 1992-08-27 |
AU650234B2 (en) | 1994-06-16 |
WO1990012816A1 (en) | 1990-11-01 |
EP0470171B1 (en) | 1996-12-04 |
CA2053266A1 (en) | 1990-10-26 |
KR940003857B1 (ko) | 1994-05-04 |
DE69029324T2 (de) | 1997-04-30 |
ATE145925T1 (de) | 1996-12-15 |
DE69029324D1 (de) | 1997-01-16 |
ES2097146T3 (es) | 1997-04-01 |
EP0470171A4 (en) | 1992-10-28 |
AU5655790A (en) | 1990-11-16 |
JP3021037B2 (ja) | 2000-03-15 |
EP0470171A1 (en) | 1992-02-12 |
US5270276A (en) | 1993-12-14 |
CA2053266C (en) | 1999-11-30 |
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