JP5703233B2 - その場生成されるフッ素化イオノマーの分散した微粒子を使用する水性重合によって製造されるフルオロポリマー - Google Patents
その場生成されるフッ素化イオノマーの分散した微粒子を使用する水性重合によって製造されるフルオロポリマー Download PDFInfo
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- JP5703233B2 JP5703233B2 JP2011543670A JP2011543670A JP5703233B2 JP 5703233 B2 JP5703233 B2 JP 5703233B2 JP 2011543670 A JP2011543670 A JP 2011543670A JP 2011543670 A JP2011543670 A JP 2011543670A JP 5703233 B2 JP5703233 B2 JP 5703233B2
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- 150000001340 alkali metals Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- ORBBVPFDROYXQS-UHFFFAOYSA-N ammonium perfluorononanoate Chemical compound N.OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ORBBVPFDROYXQS-UHFFFAOYSA-N 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005311 autocorrelation function Methods 0.000 description 1
- YOALFLHFSFEMLP-UHFFFAOYSA-N azane;2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoic acid Chemical compound [NH4+].[O-]C(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YOALFLHFSFEMLP-UHFFFAOYSA-N 0.000 description 1
- HYGWNUKOUCZBND-UHFFFAOYSA-N azanide Chemical compound [NH2-] HYGWNUKOUCZBND-UHFFFAOYSA-N 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000005341 cation exchange Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000003843 chloralkali process Methods 0.000 description 1
- 229910001902 chlorine oxide Inorganic materials 0.000 description 1
- QABCGOSYZHCPGN-UHFFFAOYSA-N chloro(dimethyl)silicon Chemical compound C[Si](C)Cl QABCGOSYZHCPGN-UHFFFAOYSA-N 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 229920001198 elastomeric copolymer Polymers 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010096 film blowing Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- UODYGZNFOZNALS-UHFFFAOYSA-N fluoro 2-ethenoxyethanesulfonate Chemical compound FOS(=O)(=O)CCOC=C UODYGZNFOZNALS-UHFFFAOYSA-N 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 239000004446 fluoropolymer coating Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000004966 inorganic peroxy acids Chemical class 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000004702 methyl esters Chemical group 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- GSWAOPJLTADLTN-UHFFFAOYSA-N oxidanimine Chemical compound [O-][NH3+] GSWAOPJLTADLTN-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- ZWBAMYVPMDSJGQ-UHFFFAOYSA-N perfluoroheptanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZWBAMYVPMDSJGQ-UHFFFAOYSA-N 0.000 description 1
- 229920005548 perfluoropolymer Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
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
- C08F14/00—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 a halogen
- C08F14/18—Monomers containing fluorine
-
- 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
- C08F214/00—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 a halogen
- C08F214/18—Monomers containing fluorine
-
- 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
- C08F259/00—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00
- C08F259/08—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing fluorine
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14011808P | 2008-12-23 | 2008-12-23 | |
| US61/140,118 | 2008-12-23 | ||
| PCT/US2009/069370 WO2010075496A1 (en) | 2008-12-23 | 2009-12-23 | Fluoropolymer produced by aqueous polymerization using dispersed particulate of fluorinated ionomer produced in situ |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012513534A JP2012513534A (ja) | 2012-06-14 |
| JP2012513534A5 JP2012513534A5 (enExample) | 2013-02-07 |
| JP5703233B2 true JP5703233B2 (ja) | 2015-04-15 |
Family
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| JP2011543670A Expired - Fee Related JP5703233B2 (ja) | 2008-12-23 | 2009-12-23 | その場生成されるフッ素化イオノマーの分散した微粒子を使用する水性重合によって製造されるフルオロポリマー |
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| EP (1) | EP2367861B1 (enExample) |
| JP (1) | JP5703233B2 (enExample) |
| CN (1) | CN102264775B (enExample) |
| WO (1) | WO2010075496A1 (enExample) |
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| US20100036053A1 (en) * | 2008-08-08 | 2010-02-11 | E.I. Du Pont De Nemours And Company | Aqueous Polymerization Process for the Manufacture of Fluoropolymer Comprising Repeating Units Arising from a Perfluoromonomer and a Monomer Having a Functional Group and a Polymerizable Carbon-Carbon Double Bond |
| US8153738B2 (en) * | 2008-12-23 | 2012-04-10 | E I Du Pont De Nemours And Company | Fluoropolymer produced by aqueous polymerization using dispersed particulate of fluorinated ionomer |
| US9012025B2 (en) * | 2012-04-05 | 2015-04-21 | Xerox Corporation | Fuser member |
| JP5665800B2 (ja) | 2012-06-22 | 2015-02-04 | 三井・デュポンフロロケミカル株式会社 | テトラフルオロエチレン／パーフルオロ（アルキルビニルエーテル）共重合体 |
| EP2882705B1 (en) | 2012-08-10 | 2018-02-21 | Solvay Specialty Polymers Italy S.p.A. | Allyl-bearing fluorinated ionomers |
| US9243080B2 (en) * | 2012-11-30 | 2016-01-26 | Daikin Industries, Ltd. | Production method for polytetrafluoroethylene aqueous dispersion |
| US20150210787A1 (en) * | 2012-12-18 | 2015-07-30 | E. I. Du Pont De Nemours And Company | Process for Producing Fluoroelastomers |
| EP3027684B1 (en) * | 2013-07-30 | 2017-05-17 | Solvay Specialty Polymers Italy S.p.A. | Fluorine-containing thermoplastic elastomer composition |
| US10644339B2 (en) | 2013-11-29 | 2020-05-05 | Asahi Kasei Kabushiki Kaisha | Polymer electrolyte membrane |
| KR20160090381A (ko) * | 2013-11-29 | 2016-07-29 | 아사히 가세이 가부시키가이샤 | 고분자 전해질막 |
| US11084895B2 (en) | 2013-11-29 | 2021-08-10 | Daikin Industries, Ltd. | Modified polytetrafluoroethylene fine powder and uniaxially stretched porous body |
| EP3075767B1 (en) | 2013-11-29 | 2025-04-16 | Daikin Industries, Ltd. | Porous body, polymer electrolyte membrane, filter material for filter, and filter unit |
| JP6395411B2 (ja) * | 2014-03-25 | 2018-09-26 | 三井・ケマーズ フロロプロダクツ株式会社 | テトラフルオロエチレンとパーフルオロ（エチルビニルエーテル）との共重合体を含む複合成形体 |
| WO2019055791A1 (en) | 2017-09-14 | 2019-03-21 | 3M Innovative Properties Company | FLUORINATED COPOLYMER HAVING SULFONYL PENDANT GROUPS AND COMPOSITIONS AND ARTICLES COMPRISING SAID FLUORINATED COPOLYMER |
| CN116622018A (zh) | 2018-03-01 | 2023-08-22 | 大金工业株式会社 | 含氟聚合物的制造方法 |
| US12195617B2 (en) | 2018-11-19 | 2025-01-14 | Daikin Industries, Ltd. | Composition and stretched body |
| CN113039213B (zh) * | 2018-11-19 | 2023-07-28 | 大金工业株式会社 | 改性聚四氟乙烯的制造方法和组合物 |
| EP3960713A4 (en) | 2019-04-26 | 2023-01-18 | Daikin Industries, Ltd. | Water treatment method and composition |
| CN113728014B (zh) | 2019-04-26 | 2024-07-26 | 大金工业株式会社 | 含氟聚合物水性分散液的制造方法、排水的处理方法和含氟聚合物水性分散液 |
| JP7368759B2 (ja) | 2019-09-05 | 2023-10-25 | ダイキン工業株式会社 | パーフルオロエラストマーの製造方法および組成物 |
| WO2021045227A1 (ja) | 2019-09-05 | 2021-03-11 | ダイキン工業株式会社 | 組成物およびその製造方法 |
| JP7352110B2 (ja) | 2019-11-19 | 2023-09-28 | ダイキン工業株式会社 | フルオロポリマーの製造方法、ポリテトラフルオロエチレンの製造方法、パーフルオロエラストマーの製造方法および組成物 |
| CN111114836B (zh) * | 2019-12-31 | 2021-07-06 | 上海空间推进研究所 | 大尺寸高基频轻量化表面张力贮箱 |
| CN111690092B (zh) * | 2020-06-03 | 2022-04-19 | 乳源东阳光氟树脂有限公司 | 一种聚偏氟乙烯表面改性的核壳结构锂电池粘结剂及其制备方法和应用 |
| CN112409528B (zh) * | 2020-10-21 | 2021-11-16 | 浙江巨化技术中心有限公司 | 一种核壳结构ptfe分散树脂的制备方法 |
| WO2022107894A1 (ja) | 2020-11-19 | 2022-05-27 | ダイキン工業株式会社 | ポリテトラフルオロエチレンの製造方法およびポリテトラフルオロエチレンを含有する組成物 |
| JP7709062B2 (ja) | 2020-11-19 | 2025-07-16 | ダイキン工業株式会社 | 含フッ素エラストマー水性分散液の製造方法および組成物 |
| EP4249525A4 (en) | 2020-11-19 | 2024-10-16 | Daikin Industries, Ltd. | METHOD FOR PREPARING AN AQUEOUS PERFLUOROLASTOMER DISPERSION, COMPOSITION, CROSS-LINKABLE COMPOSITION AND CROSS-LINKED PRODUCT |
| JP7727213B2 (ja) | 2021-03-10 | 2025-08-21 | ダイキン工業株式会社 | 塗料組成物、塗布膜、積層体および塗装物品 |
| JPWO2022244784A1 (enExample) | 2021-05-19 | 2022-11-24 | ||
| CN117529511A (zh) | 2021-06-11 | 2024-02-06 | 大金工业株式会社 | 含氟弹性体水性分散液的制造方法、组合物和水性分散液 |
| EP4365211A4 (en) | 2021-06-30 | 2025-07-16 | Daikin Ind Ltd | METHOD FOR PRODUCING A COMPOSITION CONTAINING A HIGH-PURITY FLUOROPOLYMER, AND COMPOSITION CONTAINING A HIGH-PURITY FLUOROPOLYMER |
| JP7747987B2 (ja) | 2021-06-30 | 2025-10-02 | ダイキン工業株式会社 | フルオロポリマー組成物の製造方法およびフルオロポリマー組成物 |
| CN113549168B (zh) * | 2021-08-19 | 2023-01-20 | 常熟三爱富中昊化工新材料有限公司 | 聚三氟苯乙烯的制备方法 |
| EP4497762A1 (en) | 2022-03-23 | 2025-01-29 | Daikin Industries, Ltd. | Method for producing fluoropolymer, and composition |
| EP4516819A1 (en) | 2022-04-28 | 2025-03-05 | Daikin Industries, Ltd. | Method for producing fluoropolymer |
| WO2023210818A1 (ja) | 2022-04-28 | 2023-11-02 | ダイキン工業株式会社 | フッ素ゴムを含有する組成物 |
| WO2023210820A1 (ja) * | 2022-04-28 | 2023-11-02 | ダイキン工業株式会社 | フッ素樹脂を含有する組成物の製造方法およびフッ素樹脂を含有する組成物 |
| WO2024154773A1 (ja) | 2023-01-18 | 2024-07-25 | ダイキン工業株式会社 | テトラフルオロエチレン系ポリマー組成物、電気化学デバイス用バインダー、電極合剤、電極、及び、二次電池 |
| CN120548621A (zh) | 2023-01-18 | 2025-08-26 | 大金工业株式会社 | 电化学器件用合剂、电化学器件用合剂片、电极和电化学器件 |
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-
2009
- 2009-12-18 US US12/641,374 patent/US8058376B2/en not_active Expired - Fee Related
- 2009-12-23 EP EP09796576.8A patent/EP2367861B1/en not_active Not-in-force
- 2009-12-23 CN CN200980152388.4A patent/CN102264775B/zh not_active Expired - Fee Related
- 2009-12-23 JP JP2011543670A patent/JP5703233B2/ja not_active Expired - Fee Related
- 2009-12-23 WO PCT/US2009/069370 patent/WO2010075496A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| US20100160510A1 (en) | 2010-06-24 |
| JP2012513534A (ja) | 2012-06-14 |
| CN102264775B (zh) | 2014-05-07 |
| WO2010075496A1 (en) | 2010-07-01 |
| CN102264775A (zh) | 2011-11-30 |
| US8058376B2 (en) | 2011-11-15 |
| EP2367861A1 (en) | 2011-09-28 |
| EP2367861B1 (en) | 2015-02-25 |
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