KR900701720A - 교체되는 폴리알킬렌과 호박산 그룹을 갖는 신규 중합 분산제 - Google Patents
교체되는 폴리알킬렌과 호박산 그룹을 갖는 신규 중합 분산제Info
- Publication number
- KR900701720A KR900701720A KR1019900701134A KR900701134A KR900701720A KR 900701720 A KR900701720 A KR 900701720A KR 1019900701134 A KR1019900701134 A KR 1019900701134A KR 900701134 A KR900701134 A KR 900701134A KR 900701720 A KR900701720 A KR 900701720A
- Authority
- KR
- South Korea
- Prior art keywords
- copolymer
- molecular weight
- polysuccinimide
- lower alkyl
- carbon atoms
- Prior art date
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- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Laminated Bodies (AREA)
Abstract
내용 없음
Description
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Claims (70)
- 생성된 공중합체가 윤활유중에 용해될 수 있을만큼 충분히 많은 탄소원자를 함유하며 총 올레핀의 20%이상이 알키비닐리덴 이성체로 이루어진 고분자량의 올레핀과 불포화 산성 반응물과의 공중합체.
- 제1항에 있어서, 총 올레핀의 50%이상이 알킬비닐리덴 이성체인 공중합체.
- 제2항에 있어서, 불포화 산성 반응물이 다음 일반식으로 표시되는 공중합체;상기식에서, X 및 X′는 각각 독립적으로 -OH, -Cl, 및 -0-저급 알킬로 이루어진 그룹중에서 선택되거나, X와 X′는 함께 취할 경우 -O-이다.
- 제3항에 있어서, 평균 중합도가 1.0이상인 공중합체.
- 제4항에 있어서, 올레핀의 평균 분자량이 약 500 내지 약 500인 공중합체.
- 제5항에 있어서, 올레핀이 폴리이소부텐인 공중합체.
- 제6항에 있어서, 평균 중합도가 약 1.5 내지 약 10인 공중합체.
- 제7항에 있어서, 산성반응물이 말레산 무수물로 이루어진 공중합체.
- 제8항에 있어서, 폴리이소부텐의 평균분자량이 약 900내지 약 200인 공중합체.
- 제9항에 있어서, 총 올레핀중 약 70%이상이 알킬비닐리덴 이성체로 이루어진 공중합체.
- 제10항에 있어서, 알킬비닐리덴 이성체가 메틸비닐리덴인 공중합체.
- 다음 일반식의 공중합체 :상기식에서, n은 1이상이고, R1, R2, R3및 R4는 수소, 탄소수 1 내지 6의 저급알킬 및 고분자량의 폴리알킬중에서 선택되거나; R1및 R2가 수소이고, R3및 R4중 하나가 저급알킬이며, 다른 하나가 고분자량의 폴리알킬이거나; R3및 R4가 수소이고, R1및 R2중 하나가 저급알킬이며, 다른 하나가 고분자량의 폴리알킬이다.
- 제12항에 있어서, 고분자량의 폴리알킬이 탄소원자 약50개 이상으로 이루어진폴리이소부티그룹 공중합체.
- 제13항에 있어서, 폴리이소부틸그룹의 평균분자량이 약 500 내지 5000인 공중합체.
- 제14항에 있어서, 폴리이소부틸그룹의 평균분자량이 약 900 내지 2500인 공중합체.
- 제15항에 있어서, 평균 중합도가 약 1.1 내지 약 20인 공중합체.
- 제16항에 있어서, 저급알킬이 메틸인 공중합체.
- 총 고분자량의 올레핀 중 약20%이상이 알킬비닐리덴 이성체로 이루어져 있고 상기 고분자량의 올레핀이 생성물이 윤활유중에 용해될 수 있을 만큼 충분히 많은 탄소원자를 함유하는 고분자량의 올레핀을 유리기 개시제의 존재하에서 불포화 산성반응물과 반응시킴을 특징으로 하는 방법에 의하여 제조된 생성물.
- 제18항에 있어서, 불포화 산성반응물의 일반식이 다음과 같은 생성물 :상기식에서, X 및 X′는 각각 독립적으로 -OH, -Cl, 및 -0-저급 알킬로 이루어진 그룹중에서 선택되거나, X와 X′는 함게 취할 경우 -0-이다.
- 제19항에 있어서, 총 올레핀중 50%이상이 알킬비닐리덴 이성체로 이루어진 생성물.
- 제20항에 있어서, 고분자량의 올레핀의 평균분자량이 약 500 내지 약 5000인 생성물.
- 제21항에 있어서, 고분자량의 올레핀이 폴리이소부테인 생성물.
- 제22항에 있어서, 평균중합도가 약 1.5 내지 약 10인 생성물.
- 제23항에 있어서, 산선반응물이 말레산무수물이고, 알킬비닐리덴 이성체가 메틸비닐리덴인 생성물.
- 제1항, 제6항 또는 제11항에 있어서, 적외선 스펙트로스코피로 측정할 때 특이한 적외선 숙신산 무수물 스트레취가 약 1775㎝-1내지 약 1784㎝-1의 범위에 있는 공중합체.
- 제1항, 제6항 또는 제11항의 공중합체을 하나이상의 염기성 절소원자를 함유하는 폴리아민과 반응시켜 제조한 폴리숙신이미드.
- 제26항에 있어서, 적외선 스텍트로스코피로 측정할 때 특이한 적외선 숙신아미드 스트레취가 약 1697㎝-1내지 약 1703㎝-1의 범위에 있는 폴리 숙신이미드.
- 제26항에 있어서, 폴리아민이 약 2 내지 약 12개의 아민질소원자 및 약 2 내지 약 40개의 탄소원자를 함유하는 폴린숙신이미드.
- 제28항에 있어서, 폴리아민이 일반식 H2N(YNH)pH를 가지며, 이때 Y가 탄소수 2 내지 6의 알킬렌이고, p가 1 내지 6의 정수인 폴리숙신이미드.
- 제29항에 있어서, 공중합체중의 폴리아민 대 숙신산그룹의 충전몰비가 약 1내지 약0. 1인 폴리숙신이미드.
- 제29항에 있어서, 공중합체중의 폴리아민 대 숙신산그룹의 충전몰비가 약 0.5인 폴리숙신이미드.
- 다음 일반식의 화합물 :상기식에서, n은 1이상이고: Am은 0 내지 약 10개의 아민질소원자 및 약 2 내지 약40개의 탄소원자를 함유하며: R1, R2, R3및 R4는 수소, 탄소수 1 내지 6의 저급알킬 및 고분자량의 폴리알킬 중에서 선택되거나; R1및 R2가 수소이고, R3및 R4중 하나는 저급알킬이며, 다른 하나는 고분자량의 폴리알킬이거나; R3및 R4가 수소이고, R1및 R2중 하나가 저급알킬이고, 다른 하나가 고분자량의 폴리알킬이며, R5및 R6는 독립적으로 수소, 탄소수 1 내지 5의 저급알킬, 또는 페닐이거나, 함께 취할 경우 탄소수 3 내지 6의 알킬렌으로 환을 형성한다.
- 제32항에 있어서, 고분자량의 폴리알킬이 탄소수 약50개 이상의 폴리이소부틸그룹으로 이루어진 화합물.
- 제33항에 있어서, 폴리이소부틸그룹의 평균분자량이 약 500 내지 약 5000인 화합물.
- 제34항에 있어서, Am이 일반식 〔(ZNH0pZ′)〕를 가지며 Z 및 Z′가 독립적으로 탄소수 2 내지 6의 알킬렌이고, P가 1 내지 6의 정수이며 R 및 R가 수소인 화합물.
- 제35항에 있어서, 평균중합도가 약 1.1 내지 약 20인 화합물.
- 제36항에 있어서, 폴리이소부틸그룹의 평균분자량이 약 900 내지 약 2500인 화합물.
- 제37항에 있어서, 저급알킬이 메틸인 화합물.
- 제38항에 있어서, 평균중합도가 약 1.5 내지 약 10인 화합물.
- 제37항에 있어서, Z 및 Z′가 에틸렌이고, P가 2, 3 또는 4인 화합물.
- 다음 일반식 A 및 B중에서 선택된 단위로 이루어진 랜덤 폴리숙신이미드:상기식에서, Am은 약 0 내지 약 10개의 아민질소원자 및 약 2 내지 약 40개의 탄소원자를 함유하는 연결 그룹이고: R1, R2, R3, R4, R1′, R2′, R3′, R4′, R1″, R2″, R3″, 및 R4″는 수소, 탄소수1 내지 6의 저급알킬 및 저분자량의 폴리알킬 중에서 선택되거나: R1및 R2는 수소이고, R3및 R4중 하나는 저급알킬이고, 다른 하나는 폴리알킬이거나, R3및 R4는 수소이고, R1및 R2중 하나는 저급알킬이고 다른 하나는 폴리알킬이고; R3및 R4중 하나는 R3및 R4중 하나는 저급알킬이고 다른 하나는 폴리알킬이거나, R3′ 및 R4′는 수소이고, R1′ 및 R2′중 하나는 저급알킬이고 다른 하나는 폴리알킬이며, R1″ 및 R2″는 수소이고, R3″ 및 R4″중 하나는 저급알킬이고 다른 하나는 폴리알킬이거나 R3″ 및 R4″중 수소이고 R1″ 및 R|2″중 하나는 저급알킬이고, 다른 하나는 폴리알킬이고: R5및 R6는 독립적으로 수소, 탄소수 1 내지 6의 저급알킬, 또는 페닐이거나 함께 결합할 경우 탄소수 3 내지 6의 알킬렌으로서 환을 형성하며; a, a′, b, b′는 공유결합을 위한 위치이며, 단 각 단위의 하나 이상의 a 또는 a′위치는 하나의 b 또는 b′위치에 공유결합되어야 한다.
- 제41항에 있어서, 고분자량의 폴리알킬이 탄소수 약50이상의 이소부틸그룹을 함유하는 랜덤 폴리숙신이미드.
- 제42항에 있어서, 폴리이소부틸그룹의 평균분자량이 약 500 내지 5000인 랜덤 폴리숙신이미드.
- 제43항에 있어서, Am이 일반식 -〔(ZNH0pZ′)〕-을 가지며 Z가 탄소수 2 내지 6의 알킬렌이고, Z′가 탄소수 2 내지 6의 알킬렌이며, P가 0 내지 5의 정수이고, R5및 R6가 수소인 랜덤폴리숙신이미드.
- 제44항에 있어서, A 및 B단위의 합의 평균이 약 2 내지 약 50인 랜덤 폴리숙신이미드.
- 제45항에 있어서, 폴리이소부틸그룹의 평균분자량이 약 900 내지약 2500인 랜덤 폴리신이미드.
- 제46항에 있어서, 저급 알킬이 메틸인 랜덤 폴리신이미드.
- 제47항에 있어서, A단위 보다 약 10배 만큼 많은 B단위를 함유하는 랜덤 폴리신이미드.
- 제48항에 있어서, Z 및 Z′가 에틸렌이고 P가 1, 2 또는 3인 랜덤 폴리숙신이미드.
- 개솔린 또는 디이젤 범위에서 비등하는 탄화수소 및 약30 내지 약5000ppm의 제11항에 따른 공중합체를 함유하는 연료조성물.
- 개솔린 또는 디이젤 범위에서 비등하는 탄화수소 및 약30내지 약5000ppm의 제29항에 따른 공중합체를 함유하는 연료조성물.
- 개솔린 또는 디이젤 범위에서 비등하는 탄화수소 및 약30 내지 약5000ppm의 제40항에 따른 화합물을 조성하는 연료조성물.
- 개솔린 또는 디이젤 범위에서 비등하는 탄화수소 및 약30 내지 약5000ppm의 제49항에 따른 렌덤 폴리 숙신 이미드를 함유하는 연료조성물.
- 150℉ 내지 400℉의 범위에서 비등하는 불활성의 안정한 친유성 유기용매 및 약 5 내지 약 50중량%의 제11항에 따른 공중합체를 함유하는 연료농축물.
- 150℉ 내지 400℉의 범위에서 비등하는 불활성의 안정한 친유성 유기용매 및 약 5 내지 약 50중량%의 제29항에 따른 폴리숙신 이미드를 함유하는 연료농축물.
- 150℉ 내지 400℉의 범위에서 비등하는 불활성의 안정한 친유성 유기용매 및 약 5 내지 약 50중량%의 제40항에 따른 화합물을 함유하는 연료농축물.
- 150℉ 내지 400℉의 범위에서 비등하는 불활성의 안정한 친유성 유기용매 및 약 5 내지 약 50중량%의 제49항에 따른 렌덤 폴리숙신 이미드를 함유하는 연료농축물.
- 윤활점성 있는 오일 및 분산제 유효량의 제11항에 따른 공중합체를 함유하는 윤활유 조성물.
- 윤활점성 있는 오일 및 분산제 유효량의 제29항에 따른 폴리숙신 이미드를 함유하는 윤활유 조성물.
- 윤활점성 있는 오일 및 분산제 유효량의 제40항에 따른 화합물을 함유하는 윤활유 조성물.
- 윤활점성 있는 오일 및 분산제 유효량의 제49항에 따른 렌덤 폴리숙신 이미드를 함유하는 윤활유 조성물.
- 약 90 내지 약 50중량%의 윤활점성 있는 오일 및 약 10 내지 약 50중량%의 제11항에 따른 공중합체를 함유하는 윤활유 농축물.
- 약 90 내지 약 50중량%의 윤활점성 있는 오일 및 약 10 내지 약 50중량%의 제29항에 따른 폴리숙신 이미드를 함유하는 윤활유 농축물.
- 약 90 내지 약 50중량%의 윤활점성 있는 오일 및 약 10 내지 약 50중량%의 제40항에 따른 화합물을 함유하는 윤활유 농축물.
- 약90 내지 약50중량%의 윤활점성 있는오일 및 약10 내지 약50중량%의 제49항에 따른 랜덤 폴리숙신 이미드를 함유하는 윤활유 농축물.
- 하나이상의 1급 또는 2급아민 그룹을 함유하는 제26항에 따른 폴리숙신이미드를 사이클릭카보네이트 또는 직쇄의 모노-또는 폴리-카보네이트와 반응시킴을 특징으로 하는 방법에 의해 제조된 생성물.
- 제66항에 있어서, 폴리숙신이미드를 사이클릭카보네이트와 반응시킨 생성물.
- 제67항에 있어서, 사이클릭카보네이트가 에틸렌 카보네이트인 생성물.
- 제26항에 따른 폴리숙신이미드를 산화붕소, 할로겐화붕소, 붕산 및 붕산의 에스테르로 이루어진 그룹중에서 선택된 붕소화합물과 반응시킴을 특징으로 하는 방법에 의해 제조된 생성물.
- 제69항에 있어서, 붕소화합물이 붕산인 생성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US25161388A | 1988-09-29 | 1988-09-29 | |
US251,613 | 1988-09-29 | ||
PCT/US1989/004270 WO1990003359A1 (en) | 1988-09-29 | 1989-09-29 | Novel polymeric dispersants having alternating polyalkylene and succinic groups |
Publications (1)
Publication Number | Publication Date |
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KR900701720A true KR900701720A (ko) | 1990-12-04 |
Family
ID=22952699
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900701134A KR900701720A (ko) | 1988-09-29 | 1989-09-29 | 교체되는 폴리알킬렌과 호박산 그룹을 갖는 신규 중합 분산제 |
Country Status (10)
Country | Link |
---|---|
EP (2) | EP0387346B1 (ko) |
JP (1) | JP3174305B2 (ko) |
KR (1) | KR900701720A (ko) |
AT (1) | ATE123753T1 (ko) |
AU (1) | AU637332B2 (ko) |
BR (1) | BR8907104A (ko) |
CA (1) | CA1338893C (ko) |
DE (2) | DE68923076T2 (ko) |
FI (1) | FI902652A0 (ko) |
WO (1) | WO1990003359A1 (ko) |
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JPH07309943A (ja) * | 1994-05-16 | 1995-11-28 | Mitsubishi Chem Corp | 酸性アミノ酸系樹脂 |
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US5889072A (en) * | 1997-02-24 | 1999-03-30 | Solutia Inc. | Process for preparing superabsorbing crosslinked polyaspartate salt |
US5834568A (en) * | 1997-03-17 | 1998-11-10 | Solutia, Inc. | Forming crosslinked polysuccinimide |
US5859179A (en) * | 1997-03-17 | 1999-01-12 | Solutia Inc. | Forming superabsorbent polymer |
US5981761A (en) * | 1997-03-27 | 1999-11-09 | Solutia Inc. | Crosslinked polyaspartate salts a process for their production |
US6165235A (en) * | 1997-08-26 | 2000-12-26 | The Lubrizol Corporation | Low chlorine content compositions for use in lubricants and fuels |
US6310134B1 (en) * | 1998-06-30 | 2001-10-30 | Eastman Chemical Company | Adhesion-promoting primer compositions for polyolefin substrates |
US6015776A (en) * | 1998-09-08 | 2000-01-18 | Chevron Chemical Company | Polyalkylene polysuccinimides and post-treated derivatives thereof |
DE19847868C2 (de) * | 1998-10-16 | 2003-09-25 | Clariant Gmbh | Sprengstoffe, enthaltend modifizierte Copolymere aus Polyisobutylen und Maleinsäureanhydrid als Emulgatoren |
DE19901803B4 (de) | 1999-01-19 | 2005-04-07 | Clariant Gmbh | Copolymere und ihre Verwendung als Additiv zur Verbesserung der Kaltfließeigenschaften von Mitteldestillaten |
DE19948111A1 (de) | 1999-10-06 | 2001-04-12 | Basf Ag | Verfahren zur Herstellung Polyisobutenphenol-haltiger Mannichaddukte |
DE19948114A1 (de) | 1999-10-06 | 2001-04-12 | Basf Ag | Verfahren zur Herstellung Polyisobutenphenol-haltiger Mannichaddukte |
US6451920B1 (en) * | 1999-11-09 | 2002-09-17 | Chevron Chemical Company Llc | Process for making polyalkylene/maleic anhydride copolymer |
DE10003297C2 (de) | 2000-01-27 | 2003-08-21 | Clariant Gmbh | Sprengstoffe, enthaltend modifizierte Copolymere aus Polyisobutylen, Vinylestern und Maleinsäureanhydrid als Emulgatoren |
AU5498301A (en) * | 2000-05-12 | 2001-11-20 | Associated Octel Company Limited, The | Diesel fuel stabiliser |
DE102004007501A1 (de) | 2004-02-13 | 2005-09-01 | Basf Ag | Amphiphile Blockcopolymere enthaltende wässrige Polymerdispersionen, Verfahren zu ihrer Herstellung und ihre Verwendung |
US7645728B2 (en) * | 2004-02-17 | 2010-01-12 | Afton Chemical Corporation | Lubricant and fuel additives derived from treated amines |
US7879774B2 (en) * | 2004-07-19 | 2011-02-01 | Afton Chemical Corporation | Titanium-containing lubricating oil composition |
CN101326239A (zh) | 2005-12-05 | 2008-12-17 | 埃克森美孚化学专利公司 | 用于弹性体组合物的加工助剂 |
WO2007070063A1 (en) | 2005-12-16 | 2007-06-21 | Exxonmobil Chemical Patents Inc. | Processing aids for elastomeric compositions |
DE102007044933A1 (de) | 2006-09-20 | 2008-05-29 | Basf Se | Verfahren zur Herstellung von Polyisobuten |
US8859473B2 (en) | 2008-12-22 | 2014-10-14 | Chevron Oronite Company Llc | Post-treated additive composition and method of making the same |
CN102753198B (zh) | 2009-12-18 | 2014-08-27 | 巴斯夫欧洲公司 | 用于加溶低溶解性活性成分的具有疏水性核的超支化聚酯 |
JP2013514402A (ja) | 2009-12-18 | 2013-04-25 | ビーエーエスエフ ソシエタス・ヨーロピア | 難溶性活性成分を可溶化するための疎水性中核部を有する超分岐ポリエステル |
RU2594563C2 (ru) * | 2014-06-20 | 2016-08-20 | Федеральное государственное бюджетное учреждение науки Институт органической химии Уфимского научного центра Российской академии наук (ИОХ УНЦ РАН) | Способ получения алкенилсукцинимидов 1,2-дизамещенных имидазолина |
RU2670453C1 (ru) * | 2017-11-07 | 2018-10-23 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Башкирский государственный университет" | Способ получения алкенилфталамидосукцинимидов |
RU2670452C1 (ru) * | 2017-11-07 | 2018-10-23 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Башкирский государственный университет" | Способ получения алкенилсукцинцианэтилимидов 1,2-дизамещённых имидазолина |
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US2977334A (en) * | 1956-10-04 | 1961-03-28 | Monsanto Chemicals | Derivatives of ethylene/maleic anhydride copolymers |
DE1921362A1 (de) * | 1969-04-26 | 1970-11-19 | Bayer Ag | Verfahren zur Herstellung von sauer anfaerbbaren Polyacrylnitril-Polymerisatmischungen |
US3677725A (en) * | 1970-02-04 | 1972-07-18 | Mobil Oil Corp | Liquid hydrocarbon compositions containing antistatic agents |
US4055581A (en) * | 1974-01-02 | 1977-10-25 | Hooker Chemicals & Plastics Corporation | Heat and light stabilizers for halogen containing polymeric resins |
US4110349A (en) * | 1976-06-11 | 1978-08-29 | The Lubrizol Corporation | Two-step method for the alkenylation of maleic anhydride and related compounds |
US4416668A (en) * | 1978-10-25 | 1983-11-22 | Petrolite Corporation | Antistatic agents for organic liquids |
SE449493B (sv) * | 1979-12-13 | 1987-05-04 | Inst Francais Du Petrole | Sampolymer av en akrylsyraester, en dikarboxiforening och diisobuten, samt dess anvendning som flytegenskapsforbettrande tillsatsmedel i kolveteoljor |
SU900599A1 (ru) * | 1980-02-19 | 1985-01-15 | Институт нефтехимического синтеза им.А.В.Топчиева | Сополимеры малеинового ангирдида с алленовыми углеводородами,обладающие противовирусными свойствами |
GB2081274A (en) * | 1980-08-06 | 1982-02-17 | Orobis Ltd | Polyalkenyl bis(succinic acids or anhydrides) |
GB2081722A (en) * | 1980-08-06 | 1982-02-24 | Orobis Ltd | Alkenyl Succinic Acid/Anhydride |
US4472588A (en) * | 1981-11-25 | 1984-09-18 | Bp Chemicals Limited | Production of polyalkenyl succinic anhydrides |
US4526950A (en) * | 1982-04-20 | 1985-07-02 | The Lubrizol Corporation | Method for preparing interpolymers |
FR2539754A1 (fr) * | 1983-01-25 | 1984-07-27 | Inst Francais Du Petrole | Additifs azotes utilisables comme agents d'abaissement du point de trouble des distillats moyens d'hydrocarbures et compositions de distillats moyens d'hydrocarbures renfermant lesdits additifs |
US4548725A (en) * | 1983-05-18 | 1985-10-22 | Mobil Oil Corporation | Reducing low temperature haze formation of hydrodewaxed base stocks |
US4612132A (en) * | 1984-07-20 | 1986-09-16 | Chevron Research Company | Modified succinimides |
GB8628523D0 (en) * | 1986-11-28 | 1987-01-07 | Shell Int Research | Lubricating composition |
JPH0788370B2 (ja) * | 1986-12-27 | 1995-09-27 | 三菱化学株式会社 | アルケニルコハク酸無水物の製造法 |
-
1989
- 1989-09-29 EP EP89911336A patent/EP0387346B1/en not_active Expired - Lifetime
- 1989-09-29 BR BR898907104A patent/BR8907104A/pt not_active Application Discontinuation
- 1989-09-29 CA CA000615295A patent/CA1338893C/en not_active Expired - Lifetime
- 1989-09-29 KR KR1019900701134A patent/KR900701720A/ko not_active Application Discontinuation
- 1989-09-29 EP EP94118399A patent/EP0644208B1/en not_active Expired - Lifetime
- 1989-09-29 WO PCT/US1989/004270 patent/WO1990003359A1/en active IP Right Grant
- 1989-09-29 AT AT89911336T patent/ATE123753T1/de not_active IP Right Cessation
- 1989-09-29 JP JP51056289A patent/JP3174305B2/ja not_active Expired - Lifetime
- 1989-09-29 AU AU44030/89A patent/AU637332B2/en not_active Ceased
- 1989-09-29 DE DE68923076T patent/DE68923076T2/de not_active Expired - Lifetime
- 1989-09-29 DE DE68928707T patent/DE68928707T2/de not_active Expired - Lifetime
-
1990
- 1990-05-28 FI FI902652A patent/FI902652A0/fi not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
ATE123753T1 (de) | 1995-06-15 |
DE68923076T2 (de) | 1996-02-15 |
AU4403089A (en) | 1990-04-18 |
JPH03502698A (ja) | 1991-06-20 |
EP0644208A3 (en) | 1995-05-24 |
EP0644208A2 (en) | 1995-03-22 |
EP0644208B1 (en) | 1998-06-10 |
FI902652A0 (fi) | 1990-05-28 |
EP0387346A1 (en) | 1990-09-19 |
JP3174305B2 (ja) | 2001-06-11 |
DE68928707D1 (de) | 1998-07-16 |
DE68928707T2 (de) | 1999-01-21 |
DE68923076D1 (de) | 1995-07-20 |
EP0387346B1 (en) | 1995-06-14 |
BR8907104A (pt) | 1991-02-05 |
AU637332B2 (en) | 1993-05-27 |
WO1990003359A1 (en) | 1990-04-05 |
CA1338893C (en) | 1997-02-04 |
EP0387346A4 (en) | 1991-04-10 |
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