KR870003126A - 황경화성 실리콘 고무 - Google Patents
황경화성 실리콘 고무 Download PDFInfo
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- KR870003126A KR870003126A KR1019860007545A KR860007545A KR870003126A KR 870003126 A KR870003126 A KR 870003126A KR 1019860007545 A KR1019860007545 A KR 1019860007545A KR 860007545 A KR860007545 A KR 860007545A KR 870003126 A KR870003126 A KR 870003126A
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- South Korea
- Prior art keywords
- carbon atoms
- chlorothio
- radicals
- silicone rubber
- phenyl
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- 229920002379 silicone rubber Polymers 0.000 title claims 21
- 239000004945 silicone rubber Substances 0.000 title claims 19
- 238000004383 yellowing Methods 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 21
- -1 N-fluorothio-sulfonamide Chemical compound 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- UNOPJOFCFSFPCK-UHFFFAOYSA-N ClNS(=O)=S Chemical compound ClNS(=O)=S UNOPJOFCFSFPCK-UHFFFAOYSA-N 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 229920000459 Nitrile rubber Polymers 0.000 claims 3
- 239000007795 chemical reaction product Substances 0.000 claims 3
- 229920003244 diene elastomer Polymers 0.000 claims 3
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 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 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- WHPASJHILRGNCY-UHFFFAOYSA-N (n-(4-methylphenyl)sulfonylanilino) thiohypochlorite Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N(SCl)C1=CC=CC=C1 WHPASJHILRGNCY-UHFFFAOYSA-N 0.000 claims 1
- SZKCUXJDOKLMQQ-UHFFFAOYSA-N 1,2,8-thiadiazocane 1,1-dioxide Chemical compound O=S1(=O)NCCCCCN1 SZKCUXJDOKLMQQ-UHFFFAOYSA-N 0.000 claims 1
- YCMLQMDWSXFTIF-UHFFFAOYSA-N 2-methylbenzenesulfonimidic acid Chemical compound CC1=CC=CC=C1S(N)(=O)=O YCMLQMDWSXFTIF-UHFFFAOYSA-N 0.000 claims 1
- 244000043261 Hevea brasiliensis Species 0.000 claims 1
- 239000005062 Polybutadiene Substances 0.000 claims 1
- SQHFOJGTLRUIJQ-UHFFFAOYSA-N [(4-chlorophenyl)sulfonyl-propylamino] thiohypochlorite Chemical compound CCCN(SCl)S(=O)(=O)C1=CC=C(Cl)C=C1 SQHFOJGTLRUIJQ-UHFFFAOYSA-N 0.000 claims 1
- RKURYNQAEZHSEQ-UHFFFAOYSA-N [benzenesulfonyl(methyl)amino] thiohypochlorite Chemical compound ClSN(C)S(=O)(=O)C1=CC=CC=C1 RKURYNQAEZHSEQ-UHFFFAOYSA-N 0.000 claims 1
- LARWKEHJBYUNQQ-UHFFFAOYSA-N [dimethylsulfamoyl(methyl)amino] thiohypochlorite Chemical compound CN(C)S(=O)(=O)N(C)SCl LARWKEHJBYUNQQ-UHFFFAOYSA-N 0.000 claims 1
- ZSXOAFADVREZAE-UHFFFAOYSA-N [ethyl-(4-methylphenyl)sulfonylamino] thiohypochlorite Chemical compound CCN(SCl)S(=O)(=O)C1=CC=C(C)C=C1 ZSXOAFADVREZAE-UHFFFAOYSA-N 0.000 claims 1
- KEXXTLGOPKSSHB-UHFFFAOYSA-N [ethylsulfonyl(methyl)amino] thiohypochlorite Chemical compound CCS(=O)(=O)N(C)SCl KEXXTLGOPKSSHB-UHFFFAOYSA-N 0.000 claims 1
- UQLZIIAOPHDAJV-UHFFFAOYSA-N [methyl(methylsulfonyl)amino] thiohypochlorite Chemical group ClSN(C)S(C)(=O)=O UQLZIIAOPHDAJV-UHFFFAOYSA-N 0.000 claims 1
- NAWQKWLDGDPPJR-UHFFFAOYSA-N [methyl-(4-methylphenyl)sulfonylamino] thiohypochlorite Chemical group ClSN(C)S(=O)(=O)C1=CC=C(C)C=C1 NAWQKWLDGDPPJR-UHFFFAOYSA-N 0.000 claims 1
- AJNATCSYYVYJAI-UHFFFAOYSA-N [methylsulfonyl(propan-2-yl)amino] thiohypochlorite Chemical compound CC(C)N(SCl)S(C)(=O)=O AJNATCSYYVYJAI-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000003245 coal Substances 0.000 claims 1
- 239000011280 coal tar Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000003106 haloaryl group Chemical group 0.000 claims 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims 1
- 229920003052 natural elastomer Polymers 0.000 claims 1
- 229920001194 natural rubber Polymers 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 229920002857 polybutadiene Polymers 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims 1
- 229920003048 styrene butadiene rubber Polymers 0.000 claims 1
- 150000003464 sulfur compounds Chemical class 0.000 claims 1
- 229920003051 synthetic elastomer Polymers 0.000 claims 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/392—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
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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)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Belt Conveyors (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (18)
- 펜던트 비닐 그룹을 함유하는 실리콘 고무과 하기 일반식의 N-클로로티오-설폰아미드와의 반응생성물로 이루어짐을 특징으로 하는 황경화성 실리콘 고무.상기식에서,R1및 R2는 탄소수 1 내지 20의 알킬 라디칼, 탄소수 7 내지 20의 아르알킬라디칼, 탄소수 7 내지 20의알크아릴 라디칼 및 탄소수 6 내지 10의 할로아릴 라디칼 중에서 선택되고, R1은 또한 일반식[여기서, R3및 R4는 각각 상기의 알킬, 아르알킬 및 할로아릴 라디칼 중에서 선택되고, R3및 R4는 함께 결합되어 -CH2-n(여기서 n은 4 내지 7의 정수이다) 및 (CH2)x0(CH2)x(여기서, x는 2 내지 6의 정수이다) 주에서 선택된 라디칼을 나타낼 수 있다]의 라디칼로부터 선택된다.
- 펜던트 비닐 그룹을 함유하는 실리콘 고무와 하기 일반식의 N-클로로티오-설폰아미드와의 반응생성물로 이루어지는 황경화성 실리콘 고무와 1종 이상의 디엔고무를 함유함을 특징으로 하는 탄성중합성 혼합물상기식에서,R1및 R2는 탄소수 1 내지 20의 알킬 라디칼, 탄소수 7 내지 20의 아르알킬 라디칼, 탄소수 7 내지 20의 알크아릴 라디칼 및 탄소수 6 내지 10의 할로아릴 라디칼 중에서 선택되고, R1은 또한 일반식-[여기서, R3및 R4는 각각 상기의 알킬, 아르알킬 및 할로아릴 라디칼 중에서 선택되고, R3및 R4는 함께 결합되어 -CH2-n(여기서, n은 4 내지 7의 정수이다) 및 (CH2)x-0(CH2)x(여기서, x는 2 내지 6의 정수이다)중에서 선택된 라디칼을 나타낼 수 있다]의 라디칼로부터 선택된다.
- 제2항에 있어서, 혼합물이 황경화된 가황화물의 형태인 탄성중합성 혼합물.
- 펜던트 비닐 그룹을 함유하는 실리콘 고무와 하기 일반식의 N-클로로티오-설폰아미드와의 반응생성물로 이루어지는 황경화성 실리콘 고무와 니트릴 이루어짐을 특징으로 하는, 콜 타로 수송에 특히유용한 컨베이어 벨트.상기식에서,R1및 R2는 탄소수 1 내지 20의 알킬 라디칼, 탄소수 7 내지 20의 아르알킬 라디칼, 탄소수 7 내지 20의 알크아릴 라디칼 및 탄소수 6 내지 10의 할로아릴 라디칼 중에서 선택되고, R1은 또한 일반식[여기서, R3및 R4는 각각 상기의 알킬, 아르알킬 및 할로아릴 라디칼 중에서 선택되고, R3및 R4는 함께 결합되어 -CH2-n(여기서, n은 4 내지 7의 정수이다) 및 (CH2)xO(CH2)x(여기서, x는 2 내지 6의 정수이다)중에서 선택된 라디칼을 나타낼수 있다]의 라디칼로부터 선택된다.
- 제4항에 있어서, N-플로로티오-설폰아미드 중의 R1및 R2가 메틸그룹, 에틸그룹, 프로필그룹, 부틸그룹, 페닐그룹 및 p-클로로페닐그룹 중에서 선택되는 컨베이어 벨트.
- 제1항에 있어서, 펜던트 비닐 그룹을 함유하는 실리콘 고무가 하기의 일반식을 갖는 황경의성 실리콘고무.상기식에서,A1,A2및 A3는 동일하거나 상이하며, 탄소수 1 내지 20의 알킬그룹, 탄소수 7 내지 20의 아르알킬그룹, 탄소수 6 내지 10의 할로아릴그룹 및 페닐그룹 중에서 선택되고,Z는 탄소수 0 내지 6의 알킬렌그룹이며,n 및 m은 정수이고,은 반복단위의 분포가 무질서할 수 있음을 나타낸다.
- 제6항에 있어서, R1및 R2가 탄소수 1 내지 6의 알킬 라디칼, 페닐 라디칼, 탄소수 7 내지 10의 모노알킬 치환된 페닐 라디칼 및 탄소수 8 내지 11의 디알킬 치환된 페닐 라디칼 중에서 선택되는 황경화성 실리콘 고무.
- 제7항에 있어서, A1,A2및 A3가 탄소수 1 내지 8의 알킬그룹 및 페닐그룹 중에서 선택되는 황경화성 실리콘 고무.
- 제8항에 있어서, Z가 탄소수 0의 알킬렌그룹인 황경화성 실리콘 고무.
- 제9항에 있어서, A1,A2및 A3가 메틸그룹 및 페닐그룹 중에서 선택되는 황경화성 실리콘 고무.
- 제6항에 있어서, R1이 메틸, 3-급-부틸, 사이클로헥실, 2-에이코실, 벤질, 2-(p-H-운데실페닐)-2-프로필, 페닐, 1-나프틸, p-톨릴, 3-에틸-4-(n-도데실)페닐, p-클로로페닐 및 3-클로로-4-(n-부틸)페닐 라디칼 중에서 선택되고, R2가 메틸, 3급-부틸, 1-에이코실, 사이클로헥실, 벤질, 1-(p-n-도데실페닐)-1-에틸, 페닐, 1-나프틸, m-톨릴, 3,4-디-(n-헵틸)페닐, p-브로모페닐 및 3-클로로-4-(n-부틸)페닐 라디칼 중에서 선택되는 황경화성 실리콘 고무.
- 제10항에 있어서, N-클로로티오-설폰아미드가 N-클로로티오-N-메틸-메탄설폰아미드, N-클로로티오-N-메틸-벤젠설폰아미드, N-클로로티오-N-메틸-p-톨루엔설폰아미드, N-클로로티오-N-에틸-p-톨루엔설폰아미드, N-클로로티오-N-메틸-에탄설폰아미드, N-클로로티오-N-페닐-p-톨루엔설폰아미드, N-클로로티오-N--(2-프로필)-메탄설폰아미드, N-클로로티오-N-(1-프로필)-p-클로로벤젠설폰아미드, N-클로로티오-N-페닐-메탄설아아미드,N-클로로티오-N,N',N'-트리메틸설프아미드, N-클로로티오-N-페닐-N',N'-(펜타메틸렌)설프아미드, N-클로로티오-N-메틸-N',N-디에틸설프아미드 및 N-클로로티오-N-페닐 벤젠설폰아미드 중에서 선택되는 황경화성 실리콘 고무.
- 제12항에 있어서, 펜던트 비닐그룹을 함유하는 실리콘 고무가 하기 일반식을 갖는 황경화성 실리콘 고무.상기식에서,n 및 m은 정수이고,은 반복단위의 분포가 무질서할 수 있음을 나타낸다.
- 제3항에 있어서, 혼합물이 황경화성 실리콘 고무 2 내지 98중량% 및 1종 이상의 디엔고무 2 내지 98중량%로 이루어지는 탄성중합성 혼합물.
- 제14항에 있어서, 디엔고무가 천연고무, 합성폴리이소프렌, 니트릴고무, 폴리부타디엔 및 스티렌-부타디엔고무 중에서 선택되는 탄성중합성 혼합물.
- 제13항에 있어서, N-클로로티오-설폰아미드가 N-클로로티오-N-메틸-p- 톨루엔-설폰아미드인 황경화성 실리콘 고무.
- 제5항에 있어서, 니트릴고무 92 내지 98중량% 및 황경화성 실리콘 고무 내지 28줄양%를 함유하는 컨베이어 벨트.
- 제13항의 황경화성 실리콘 고무와 니트릴 고무와의 황경화된 혼합물을 함유함을 특징으로 하는 콜 타르 수송에 특히 유용한 컨베이어 벨트.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US773767 | 1985-09-09 | ||
| US06/773,767 US4617347A (en) | 1985-09-09 | 1985-09-09 | Sulfur curable silicone rubber |
| US773,767 | 1985-09-09 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR870003126A true KR870003126A (ko) | 1987-04-15 |
| KR930007886B1 KR930007886B1 (ko) | 1993-08-21 |
Family
ID=25099249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019860007545A KR930007886B1 (ko) | 1985-09-09 | 1986-09-09 | 황경화성 실리콘 고무 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4617347A (ko) |
| JP (1) | JP2511420B2 (ko) |
| KR (1) | KR930007886B1 (ko) |
| BR (1) | BR8604294A (ko) |
| CA (1) | CA1266944A (ko) |
| FR (1) | FR2587032B1 (ko) |
| MX (1) | MX3626A (ko) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4722379A (en) * | 1984-06-13 | 1988-02-02 | The Goodyear Tire & Rubber Company | Coating material for use on sulfur vulcanized rubber |
| US4722380A (en) * | 1984-06-13 | 1988-02-02 | The Goodyear Tire & Rubber Company | Coating material for use on sulfur vulcanized rubber |
| US5017662A (en) * | 1988-09-15 | 1991-05-21 | Exxon Chemical Patents, Inc. | Selective catalytic process for preparing N-halothiosulfonamide modified EPDM terpolymers |
| SG67536A1 (en) * | 1997-08-13 | 1999-09-21 | Mitsui Chemicals Inc | Curable rubber composition |
| US20030123917A1 (en) * | 2000-01-15 | 2003-07-03 | Boyd Willat | Tubular deformable sleeve and related apparatus |
| US20030051316A1 (en) * | 2001-08-13 | 2003-03-20 | Willat Boyd I. | Deformable grip for a writing implement |
| US7797782B2 (en) * | 2005-06-21 | 2010-09-21 | Goody Products, Inc. | Handle having a ribbed gel grip |
| JP4938586B2 (ja) * | 2007-08-08 | 2012-05-23 | 株式会社クボタ | コンバイン |
| EP2345699A1 (en) | 2010-01-14 | 2011-07-20 | Armacell Enterprise GmbH | Silicone elastomer compounds and siloxane containing elastomer blends |
| EP2351786B1 (en) * | 2010-02-01 | 2015-04-08 | Armacell Enterprise GmbH & Co. KG | Expandable polysiloxanes |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3530160A (en) * | 1968-02-09 | 1970-09-22 | Exxon Research Engineering Co | (organo- or hydrolyzable group substituted)3silyl (unsubstituted chloro- or sulfenyl chloride substituted hydrocarbylene) sulfenyl chlorides |
| US3915907A (en) * | 1974-12-16 | 1975-10-28 | Goodyear Tire & Rubber | Chlorothio-sulfonamide-modified rubbery terpolymers and their blends |
| US3970133A (en) * | 1974-12-16 | 1976-07-20 | The Goodyear Tire & Rubber Company | Chlorothio-sulfonamide-modified rubbery terpolymers and their blends |
| JPS53102949A (en) * | 1977-02-21 | 1978-09-07 | Shin Etsu Chem Co Ltd | Elastomer composition |
| JPS60137645A (ja) * | 1983-12-27 | 1985-07-22 | 横浜ゴム株式会社 | 耐熱性コンベヤベルト |
-
1985
- 1985-09-09 US US06/773,767 patent/US4617347A/en not_active Expired - Lifetime
-
1986
- 1986-08-27 CA CA000516865A patent/CA1266944A/en not_active Expired - Fee Related
- 1986-08-29 FR FR868612225A patent/FR2587032B1/fr not_active Expired - Fee Related
- 1986-09-02 MX MX362686A patent/MX3626A/es unknown
- 1986-09-08 BR BR8604294A patent/BR8604294A/pt not_active IP Right Cessation
- 1986-09-09 JP JP61212541A patent/JP2511420B2/ja not_active Expired - Lifetime
- 1986-09-09 KR KR1019860007545A patent/KR930007886B1/ko not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA1266944A (en) | 1990-03-20 |
| FR2587032B1 (fr) | 1991-01-11 |
| FR2587032A1 (fr) | 1987-03-13 |
| KR930007886B1 (ko) | 1993-08-21 |
| US4617347A (en) | 1986-10-14 |
| BR8604294A (pt) | 1987-05-05 |
| JPS62116634A (ja) | 1987-05-28 |
| JP2511420B2 (ja) | 1996-06-26 |
| MX3626A (es) | 1994-01-31 |
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