JP2016535814A5 - - Google Patents
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- Publication number
- JP2016535814A5 JP2016535814A5 JP2016552218A JP2016552218A JP2016535814A5 JP 2016535814 A5 JP2016535814 A5 JP 2016535814A5 JP 2016552218 A JP2016552218 A JP 2016552218A JP 2016552218 A JP2016552218 A JP 2016552218A JP 2016535814 A5 JP2016535814 A5 JP 2016535814A5
- Authority
- JP
- Japan
- Prior art keywords
- emulsifier
- fluorinated
- polyhydroxy
- item
- curable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 claims description 20
- 239000003995 emulsifying agent Substances 0.000 claims description 15
- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- 229920002313 fluoropolymer Polymers 0.000 claims description 9
- 239000004811 fluoropolymer Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 7
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 6
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 6
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 5
- RRZIJNVZMJUGTK-UHFFFAOYSA-N 1,1,2-trifluoro-2-(1,2,2-trifluoroethenoxy)ethene Chemical class FC(F)=C(F)OC(F)=C(F)F RRZIJNVZMJUGTK-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- -1 perfluoro allyl ethers Chemical class 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000012986 chain transfer agent Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 239000003999 initiator Substances 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 238000007348 radical reaction Methods 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 125000002015 acyclic group Chemical group 0.000 description 3
- 229930182470 glycoside Natural products 0.000 description 3
- 150000002338 glycosides Chemical class 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13190890.7 | 2013-10-30 | ||
| EP13190890.7A EP2868674B1 (en) | 2013-10-30 | 2013-10-30 | Peroxide curable fluoropolymers obtainable by polymerization using non-fluorinated polyhydroxy emulsifiers |
| PCT/US2014/062878 WO2015066166A1 (en) | 2013-10-30 | 2014-10-29 | Peroxide curable fluoropolymers obtainable by polymerization using non-fluorinated polyhydroxy emulsifiers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016535814A JP2016535814A (ja) | 2016-11-17 |
| JP2016535814A5 true JP2016535814A5 (enExample) | 2017-12-14 |
Family
ID=49510006
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016552218A Pending JP2016535814A (ja) | 2013-10-30 | 2014-10-29 | 非フッ素化ポリヒドロキシ乳化剤を使用した重合によって得ることができる過酸化物硬化性フルオロポリマー |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US10087307B2 (enExample) |
| EP (1) | EP2868674B1 (enExample) |
| JP (1) | JP2016535814A (enExample) |
| CN (1) | CN105722874A (enExample) |
| WO (1) | WO2015066166A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3059265B1 (en) * | 2015-02-23 | 2020-10-07 | 3M Innovative Properties Company | Peroxide curable fluoropolymers obtainable by polymerization with non-fluorinated emulsifiers |
| EP3350237B1 (en) | 2015-09-18 | 2020-07-08 | Solvay Specialty Polymers Italy S.p.A. | Fluoroelastomer composition |
| CN109563397B (zh) | 2016-08-10 | 2021-03-16 | 3M创新有限公司 | 氟化压敏粘合剂及其制品 |
| CN109963887A (zh) * | 2016-11-09 | 2019-07-02 | 3M创新有限公司 | 可过氧化物固化的部分氟化聚合物 |
| CN110506084A (zh) | 2017-04-11 | 2019-11-26 | 索尔维特殊聚合物意大利有限公司 | 用于制造包含氟聚合物颗粒的水性胶乳的方法 |
| US11292763B2 (en) | 2017-05-19 | 2022-04-05 | 3M Innovative Properties Company | Methods of making a polyfluorinated allyl ether and compounds relating to the methods |
| JP2021524539A (ja) | 2018-07-20 | 2021-09-13 | スリーエム イノベイティブ プロパティズ カンパニー | ペルフルオロアリルエーテルを含有するフッ化ビニリデンフルオロポリマー |
| CN115956091A (zh) * | 2020-09-07 | 2023-04-11 | 大金工业株式会社 | 改性聚四氟乙烯水性分散液 |
| TW202509090A (zh) | 2023-07-19 | 2025-03-01 | 日商Ａｇｃ股份有限公司 | 含氟彈性體之製造方法、水性分散液、固體組成物 |
| JP7792545B1 (ja) * | 2025-07-14 | 2025-12-25 | ユニマテック株式会社 | フルオロポリマー水性分散液の製造方法、フルオロモノマーの重合方法、フルオロポリマーの製造方法 |
| JP7792546B1 (ja) * | 2025-07-14 | 2025-12-25 | ユニマテック株式会社 | フルオロポリマー水性分散液の製造方法、フルオロモノマーの重合方法、フルオロポリマーの製造方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5188679A (en) | 1990-07-19 | 1993-02-23 | Kretchmer Steven D | Metal compression-spring gemstone mountings |
| WO1992006071A1 (en) | 1990-09-28 | 1992-04-16 | The Procter & Gamble Company | Phase transfer assisted process for glucamide detergents |
| US6841616B2 (en) * | 2003-03-28 | 2005-01-11 | Arkema Inc. | Polymerization of halogen-containing monomers using siloxane surfactant |
| JP5044999B2 (ja) * | 2005-09-26 | 2012-10-10 | 旭硝子株式会社 | パーフルオロエラストマー組成物およびパーフルオロゴム成形品 |
| US8580896B2 (en) * | 2006-05-10 | 2013-11-12 | Daikin Industries, Ltd. | Process for preparing fluorine-containing polymer |
| US8835551B2 (en) * | 2007-09-14 | 2014-09-16 | 3M Innovative Properties Company | Ultra low viscosity iodine containing amorphous fluoropolymers |
| WO2010053056A1 (ja) * | 2008-11-05 | 2010-05-14 | 旭硝子株式会社 | 含フッ素弾性共重合体、その製造方法および架橋ゴム |
| PL2459641T3 (pl) * | 2009-07-31 | 2017-04-28 | 3M Innovative Properties Company | Kompozycje fluoropolimeru zawierającego związek poliolu oraz sposoby ich wytwarzania |
| EP2284200A1 (en) * | 2009-07-31 | 2011-02-16 | 3M Innovative Properties Company | Aqueous fluoropolymer dispersions containing a polyol comprising at least one long chain residue and method for producing them |
| WO2011043246A1 (ja) * | 2009-10-09 | 2011-04-14 | 株式会社クレハ | 新規なフッ化ビニリデン共重合体及びその製造方法 |
| GB201012944D0 (en) | 2010-08-02 | 2010-09-15 | 3M Innovative Properties Co | Peroxide curable fluoroelastomers containing modifiers and iodine or bromine endgroups |
| FI123931B (fi) | 2010-08-05 | 2013-12-31 | Konecranes Oyj | Nostovaunukokoonpano |
| JP6272029B2 (ja) | 2010-09-15 | 2018-01-31 | スリーエム イノベイティブ プロパティズ カンパニー | 置換糖化合物及び歯科用組成物 |
| EP2803690B1 (en) * | 2013-05-17 | 2016-12-14 | 3M Innovative Properties Company | Method for reducing fluorinated emulsifiers from aqueous fluoropolymer dispersions using sugar-based emulsifiers |
| EP2803691B1 (en) * | 2013-05-17 | 2016-04-20 | 3M Innovative Properties Company | Fluoropolymer compositions containing a polyhydroxy surfactant |
-
2013
- 2013-10-30 EP EP13190890.7A patent/EP2868674B1/en active Active
-
2014
- 2014-10-29 WO PCT/US2014/062878 patent/WO2015066166A1/en not_active Ceased
- 2014-10-29 CN CN201480059721.8A patent/CN105722874A/zh active Pending
- 2014-10-29 JP JP2016552218A patent/JP2016535814A/ja active Pending
- 2014-10-29 US US15/033,301 patent/US10087307B2/en not_active Expired - Fee Related
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