KR830006157A - 플루오로카본 비닐 에테르의 제조방법 및 생성플리머 - Google Patents
플루오로카본 비닐 에테르의 제조방법 및 생성플리머 Download PDFInfo
- Publication number
- KR830006157A KR830006157A KR1019810002077A KR810002077A KR830006157A KR 830006157 A KR830006157 A KR 830006157A KR 1019810002077 A KR1019810002077 A KR 1019810002077A KR 810002077 A KR810002077 A KR 810002077A KR 830006157 A KR830006157 A KR 830006157A
- Authority
- KR
- South Korea
- Prior art keywords
- integer
- acid group
- formula
- group
- acid
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 title 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000002253 acid Substances 0.000 claims 9
- 239000000203 mixture Substances 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000000178 monomer Substances 0.000 claims 3
- -1 trifluoromonochloroethylene, trifluoroethylene Chemical group 0.000 claims 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- FGUGXWGCSKSQFY-UHFFFAOYSA-N 1,1,1,2,2-pentafluoro-2-nitrosoethane Chemical compound FC(F)(F)C(F)(F)N=O FGUGXWGCSKSQFY-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 238000006114 decarboxylation reaction Methods 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- DAFIBNSJXIGBQB-UHFFFAOYSA-N perfluoroisobutene Chemical group FC(F)=C(C(F)(F)F)C(F)(F)F DAFIBNSJXIGBQB-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims 1
- PGOMVYSURVZIIW-UHFFFAOYSA-N trifluoro(nitroso)methane Chemical compound FC(F)(F)N=O PGOMVYSURVZIIW-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/235—Saturated compounds containing more than one carboxyl group
- C07C59/305—Saturated compounds containing more than one carboxyl group containing ether groups, groups, groups, or groups
- C07C59/315—Saturated compounds containing more than one carboxyl group containing ether groups, groups, groups, or groups containing halogen
-
- 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
- C08F216/00—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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/12—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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F216/14—Monomers containing only one unsaturated aliphatic radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/15—Unsaturated ethers containing only non-aromatic carbon-to-carbon double bonds
- C07C43/16—Vinyl ethers
-
- 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
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- 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
- C08F16/00—Homopolymers and 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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F16/12—Homopolymers and 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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F16/14—Monomers containing only one unsaturated aliphatic radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (3)
- 다음 구조식(Ⅱ)의 화합물을 탈카복실화 하여 구조식(Ⅰ)의 화합물을 제조하는 방법.상기 구조식에서n은 1 또는 1이상의 정수;x'는 Cl 또는 Br;x는 F,C;,Br 또는 n〉1일 때는 이들의 혼합물을 나타내며;a는 0 또는 0 이상의 정수;b는 0 또는 0 이상의 정수;Y는 산그릅 또는 산그릅으로 쉽게 전환될 수 있는 산 유도체;Rf와 R'f는 각각 F,Cl, 퍼플루오로알킬 및 플루오로클로로알킬기 중에서 선택된 것이며;z는 F,Cl,Br,OH,NRR' 또는 OA;R 및 R'는 각각 수소, 탄소수 1이상의 알킬 및 아릴중에서 선택된 것이며;A는 알칼리금속, 4급질소 또는 R을 나타낸다.
- 적어도 한가지의 모노머는 다음 (A)그룹에서 선택한 것이며 또 다른 적어도 한가지의 모노머는 (B)그룹에서 선택한 것인, 적어도 두가지 다른 형태의 모노머들을 개시제 존재하에, 중합이 일어나기에 충분한 시간 및 온도에서 반응시켜 중합시키는 방법.(A) 다음 일반식으로 표시되는 화합물상기 구조식에서n은 1 또는 1 이상의 정수;X는 Cl,Br 또는 n〉1일때는 이들의 혼합물을 나타내며;Y는 산 그릅 또는 산그릅으로 쉽게 전환될 수 있는 산 유도체;Rf와 R'f는 각각 F,Cl, 퍼플루오로알킬 및 플루오로클로로알킬기 중에서 선택된 것이며;a는 0 또는 0 이상의 정수;b는 0 또는 0 이상의 정수;(B) 테트라플루오로에틸렌, 트리플루오로모노클로로에틸렌, 트리플루오로에틸렌, 비닐리맨 플루오라이드, 1,1-디플루오로-2,2-디클로로에틸렌, 1,1-디플루오로-2-클로로에틸렌, 헥사플루오로프로필렌, 1,1,1,3,3-펜타플루오로프로필렌, 옥타플루오로이소부틸렌, 에틸렌, 비닐클로라이드, 트리플루오로니트로소메탄, 퍼플루오로니트로소에탄 및 알킬비닐 에텔ㅡ.
- 다음 구조식의 펜던트(pendant)그룹을 가지는 폴리머 조성물상기 구조식에서n은 1또는 1이상의 정수;X는 Cl,Br 또는 n〉1일때는 이들의 혼합물을 나타내며;Y는 산 그릅 또는 산그릅으로 쉽게 전환될 수 있는 산 유도체;a는 0 또는 0 이상의 정수;b는 0 또는 0 이상의 정수;Rf와 R'f는 상기에서와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019830005799A KR850000110B1 (ko) | 1980-06-11 | 1983-12-07 | 플루오로카본 비닐에테르의 중합방법 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15853280A | 1980-06-11 | 1980-06-11 | |
US158532 | 1980-06-11 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019830005799A Division KR850000110B1 (ko) | 1980-06-11 | 1983-12-07 | 플루오로카본 비닐에테르의 중합방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830006157A true KR830006157A (ko) | 1983-09-17 |
KR840001981B1 KR840001981B1 (ko) | 1984-10-26 |
Family
ID=22568562
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019810002077A KR840001981B1 (ko) | 1980-06-11 | 1981-06-10 | 플루오로카본 비닐 에테르의 제조방법 |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0041737B1 (ko) |
JP (2) | JPS5728025A (ko) |
KR (1) | KR840001981B1 (ko) |
AT (1) | ATE9153T1 (ko) |
AU (1) | AU541096B2 (ko) |
BR (1) | BR8103714A (ko) |
CA (1) | CA1169439A (ko) |
DE (1) | DE3165764D1 (ko) |
ZA (1) | ZA813896B (ko) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4851161A (en) * | 1981-07-02 | 1989-07-25 | E. I. Du Pont De Nemours And Company | β-substituted polyfluoropropionate salts and derivatives |
US4474700A (en) * | 1981-07-02 | 1984-10-02 | E. I. Du Pont DeNemours and Company | β-Substituted polyfluoropropionate salts and derivatives |
US4576752A (en) * | 1982-07-19 | 1986-03-18 | E. I. Du Pont De Nemours And Company | β-Substituted polyfluoroethyl compounds |
US4766248A (en) * | 1982-07-19 | 1988-08-23 | E. I. Du Pont De Nemours And Company | β-substituted polyfluoroethyl compounds |
US4686300A (en) * | 1983-03-07 | 1987-08-11 | E. I. Du Pont De Nemours And Company | Polyfluoro gamma-ketoesters and 5-hydroxy gamma lactone analogues thereof |
US4513128A (en) * | 1983-06-23 | 1985-04-23 | E. I. Du Pont De Nemours And Company | Fluorinated vinyl ether copolymers having low glass transition temperatures |
US4675453A (en) * | 1983-12-27 | 1987-06-23 | E. I. Du Pont De Nemours And Company | Process and intermediates for fluorinated vinyl ether monomer |
US4595476A (en) * | 1984-07-26 | 1986-06-17 | E. I. Du Pont De Nemours And Company | Ion exchange membranes pre-expanded with di- and poly ether-glycols |
JPH0641494B2 (ja) * | 1984-08-31 | 1994-06-01 | 旭化成工業株式会社 | 架橋可能な含フツ素共重合体 |
US5252193A (en) * | 1991-11-04 | 1993-10-12 | E. I. Du Pont De Nemours And Company | Controlled roughening of reinforced cation exchange membrane |
US6274677B1 (en) * | 1997-03-31 | 2001-08-14 | Daikin Industries Ltd. | Process for the producing perfluorovinyl ethersulfonic acid derivatives and copolymer of the same |
JP2003518139A (ja) * | 1997-07-23 | 2003-06-03 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | オレフィン類の重合 |
US6326436B2 (en) | 1998-08-21 | 2001-12-04 | Dupont Dow Elastomers, L.L.C. | Fluoroelastomer composition having excellent processability and low temperature properties |
EP1109844B1 (en) | 1998-08-21 | 2004-02-18 | Dupont Dow Elastomers L.L.C. | Fluoroelastomer composition having excellent processability and low temperature properties |
JP3786838B2 (ja) * | 1999-04-15 | 2006-06-14 | 有限会社 ミレーヌコーポレーション | 含リン原子フッ素化陽イオン交換膜,その製造方法およびそれを用いたプロトン伝導型燃料電池 |
JP2004010744A (ja) * | 2002-06-06 | 2004-01-15 | Japan Atom Energy Res Inst | 大きなイオン交換容量と優れた耐酸化性を有するフッ素系高分子共重合体及びその製造方法 |
AU2003241664A1 (en) * | 2002-06-14 | 2004-02-02 | Daikin Industries, Ltd. | Method of purifying water-soluble fluorinated vinyl ether |
DE60312515T2 (de) | 2002-06-14 | 2007-10-04 | Daikin Industries, Ltd. | Verfahren zur herstellung fluorierter fluorsulfonylalkyl-vinyl-ether |
US8658707B2 (en) | 2009-03-24 | 2014-02-25 | W. L. Gore & Associates, Inc. | Expandable functional TFE copolymer fine powder, the expanded functional products obtained therefrom and reaction of the expanded products |
US9139669B2 (en) * | 2009-03-24 | 2015-09-22 | W. L. Gore & Associates, Inc. | Expandable functional TFE copolymer fine powder, the expandable functional products obtained therefrom and reaction of the expanded products |
JP5375273B2 (ja) * | 2009-03-31 | 2013-12-25 | ダイキン工業株式会社 | 1,3−ジクロロ−1,2,3,3−テトラフルオロ酸化プロピレン及びその製造方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1341087A (fr) * | 1961-12-08 | 1963-10-25 | Du Pont | Nouveaux polyéthers fluorocarbonés |
GB1038189A (en) * | 1963-08-13 | 1966-08-10 | Du Pont | Fluorocarbon ethers and the preparation thereof |
US3282875A (en) * | 1964-07-22 | 1966-11-01 | Du Pont | Fluorocarbon vinyl ether polymers |
US3321532A (en) * | 1963-10-08 | 1967-05-23 | Du Pont | Fluorocarbon ethers |
US3351619A (en) * | 1966-08-01 | 1967-11-07 | Du Pont | Crosslinkable polymers formed from iodine-containing perfluoroalkyl vinyl ethers |
JPS604806B2 (ja) * | 1975-10-28 | 1985-02-06 | 旭化成工業株式会社 | パーフロロビニルカルボン酸の製造法 |
JPS5278827A (en) * | 1975-12-26 | 1977-07-02 | Asahi Glass Co Ltd | Preparation of ester-group-containing fluorovinyl ethers |
JPS52105118A (en) * | 1976-02-27 | 1977-09-03 | Asahi Glass Co Ltd | Preparation fluorovinylether containing ester group |
GB1550874A (en) * | 1976-10-28 | 1979-08-22 | Asahi Glass Co Ltd | Process for producing fluorinated copolymer having ion-exchange groups |
JPS54109918A (en) * | 1978-02-17 | 1979-08-29 | Asahi Glass Co Ltd | Preparation of perfluorovinyl ether having fluorocarbonyl group |
-
1981
- 1981-06-10 JP JP8830281A patent/JPS5728025A/ja active Granted
- 1981-06-10 AU AU71604/81A patent/AU541096B2/en not_active Ceased
- 1981-06-10 CA CA000379509A patent/CA1169439A/en not_active Expired
- 1981-06-10 ZA ZA00813896A patent/ZA813896B/xx unknown
- 1981-06-10 AT AT81104467T patent/ATE9153T1/de not_active IP Right Cessation
- 1981-06-10 BR BR8103714A patent/BR8103714A/pt unknown
- 1981-06-10 EP EP81104467A patent/EP0041737B1/en not_active Expired
- 1981-06-10 DE DE8181104467T patent/DE3165764D1/de not_active Expired
- 1981-06-10 KR KR1019810002077A patent/KR840001981B1/ko active
-
1990
- 1990-03-23 JP JP2072253A patent/JPH02270842A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
AU7160481A (en) | 1981-12-17 |
ZA813896B (en) | 1983-01-26 |
JPH0258281B2 (ko) | 1990-12-07 |
AU541096B2 (en) | 1984-12-13 |
DE3165764D1 (en) | 1984-10-04 |
JPH0556338B2 (ko) | 1993-08-19 |
ATE9153T1 (de) | 1984-09-15 |
KR840001981B1 (ko) | 1984-10-26 |
CA1169439A (en) | 1984-06-19 |
BR8103714A (pt) | 1982-03-02 |
EP0041737B1 (en) | 1984-08-29 |
JPS5728025A (en) | 1982-02-15 |
JPH02270842A (ja) | 1990-11-05 |
EP0041737A1 (en) | 1981-12-16 |
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