JP2012526181A - フッ素ポリマー分散液からのフルオロエーテルカルボン酸または塩の熱減量 - Google Patents
フッ素ポリマー分散液からのフルオロエーテルカルボン酸または塩の熱減量 Download PDFInfo
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- JP2012526181A JP2012526181A JP2012509999A JP2012509999A JP2012526181A JP 2012526181 A JP2012526181 A JP 2012526181A JP 2012509999 A JP2012509999 A JP 2012509999A JP 2012509999 A JP2012509999 A JP 2012509999A JP 2012526181 A JP2012526181 A JP 2012526181A
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- acid
- fluoroethercarboxylic
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000002902 bimodal effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical group 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- QABCGOSYZHCPGN-UHFFFAOYSA-N chloro(dimethyl)silicon Chemical compound C[Si](C)Cl QABCGOSYZHCPGN-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 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
- 238000010908 decantation Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 230000000447 dimerizing effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- 238000010130 dispersion processing Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- COHIUILBPQNABR-UHFFFAOYSA-N dodecyl phenylmethanesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)CC1=CC=CC=C1 COHIUILBPQNABR-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- XJWSAJYUBXQQDR-UHFFFAOYSA-M dodecyltrimethylammonium bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)C XJWSAJYUBXQQDR-UHFFFAOYSA-M 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000003988 headspace gas chromatography Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000012417 linear regression Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 238000001139 pH measurement Methods 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
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000013585 weight reducing agent 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
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
- C08F6/16—Purification
-
- 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
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)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17660309P | 2009-05-08 | 2009-05-08 | |
| US61/176,603 | 2009-05-08 | ||
| PCT/US2010/033987 WO2010129842A1 (en) | 2009-05-08 | 2010-05-07 | Thermal reduction of fluoroether carboxylic acids or salts from fluoropolymer dispersions |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014161974A Division JP2014237842A (ja) | 2009-05-08 | 2014-08-08 | フッ素ポリマー分散液からのフルオロエーテルカルボン酸または塩の熱減量 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012526181A true JP2012526181A (ja) | 2012-10-25 |
| JP2012526181A5 JP2012526181A5 (enExample) | 2013-06-20 |
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|---|---|---|---|
| JP2012509999A Pending JP2012526181A (ja) | 2009-05-08 | 2010-05-07 | フッ素ポリマー分散液からのフルオロエーテルカルボン酸または塩の熱減量 |
| JP2014161974A Pending JP2014237842A (ja) | 2009-05-08 | 2014-08-08 | フッ素ポリマー分散液からのフルオロエーテルカルボン酸または塩の熱減量 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014161974A Pending JP2014237842A (ja) | 2009-05-08 | 2014-08-08 | フッ素ポリマー分散液からのフルオロエーテルカルボン酸または塩の熱減量 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8329813B2 (enExample) |
| EP (1) | EP2427506B1 (enExample) |
| JP (2) | JP2012526181A (enExample) |
| CN (1) | CN102428106B (enExample) |
| WO (1) | WO2010129842A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8329813B2 (en) * | 2009-05-08 | 2012-12-11 | E I Du Pont De Nemours And Company | Thermal reduction of fluoroether carboxylic acids or salts from fluoropolymer dispersions |
| 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 |
| US20210108063A1 (en) * | 2016-12-01 | 2021-04-15 | 3M Innovative Properties Company | Ethylene-tetrafluoroethylene copolymer dispersions and coated articles thereof |
| US11473004B2 (en) | 2016-12-02 | 2022-10-18 | University Of Wyoming | Microemulsions and uses thereof to displace oil in heterogeneous porous media |
| JP7674666B2 (ja) | 2021-01-28 | 2025-05-12 | 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 |
| EP4286426A4 (en) | 2021-01-28 | 2025-02-12 | Daikin Industries, Ltd. | Method for producing fluoropolymer composition |
| WO2025024411A1 (en) * | 2023-07-24 | 2025-01-30 | The Chemours Company Fc, Llc | Processes of fluorinated residual reduction in fluoropolymers |
| CN121712810A (zh) | 2023-08-14 | 2026-03-20 | 大金工业株式会社 | 含氟聚合物水性分散液的制造方法和含氟聚合物水性分散液 |
| WO2025217156A1 (en) | 2024-04-09 | 2025-10-16 | The Chemours Company Fc, Llc | Application of fluoropolymer dispersion stabilizers for fluorinated residuals reduction |
| CN121556052B (zh) * | 2026-01-22 | 2026-04-28 | 山东东岳未来氢能材料股份有限公司 | 全氟羧酸及其盐的电催化连续脱羧合成含氢氟醚的方法 |
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| JP2003119204A (ja) * | 2001-10-05 | 2003-04-23 | Daikin Ind Ltd | 含フッ素重合体ラテックスの製造方法 |
| JP2003267900A (ja) * | 2002-03-13 | 2003-09-25 | National Institute Of Advanced Industrial & Technology | フッ素系カルボン酸及びその塩の使用方法 |
| JP2009501808A (ja) * | 2005-07-15 | 2009-01-22 | スリーエム イノベイティブ プロパティズ カンパニー | ペルフルオロポリエーテル界面活性剤を用いるフッ素化モノマー類の水性乳化重合 |
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| DE3708780A1 (de) | 1987-03-18 | 1988-09-29 | Helio Folien Gmbh | Mehrlagige folie |
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| IT1274591B (it) | 1994-08-05 | 1997-07-18 | Ausimont Spa | Processo per la preparazione di poliossiperfluoroalcani idrogeno terminati |
| US5637748A (en) | 1995-03-01 | 1997-06-10 | E. I. Du Pont De Nemours And Company | Process for synthesizing fluorinated nitrile compounds |
| IT1295535B1 (it) | 1996-07-01 | 1999-05-12 | Ausimont Spa | Processo di polimerizzazione di vinilidenfluoruro (vdf) |
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-
2010
- 2010-05-05 US US12/774,030 patent/US8329813B2/en not_active Expired - Fee Related
- 2010-05-07 WO PCT/US2010/033987 patent/WO2010129842A1/en not_active Ceased
- 2010-05-07 EP EP10718806.2A patent/EP2427506B1/en not_active Not-in-force
- 2010-05-07 JP JP2012509999A patent/JP2012526181A/ja active Pending
- 2010-05-07 CN CN201080020380.5A patent/CN102428106B/zh not_active Expired - Fee Related
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2014
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| JP2002514190A (ja) * | 1996-11-01 | 2002-05-14 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | α―分枝フルオロアルキルカルボニルフルオリドおよびその誘導体 |
| JP2003119204A (ja) * | 2001-10-05 | 2003-04-23 | Daikin Ind Ltd | 含フッ素重合体ラテックスの製造方法 |
| JP2003267900A (ja) * | 2002-03-13 | 2003-09-25 | National Institute Of Advanced Industrial & Technology | フッ素系カルボン酸及びその塩の使用方法 |
| JP2009501808A (ja) * | 2005-07-15 | 2009-01-22 | スリーエム イノベイティブ プロパティズ カンパニー | ペルフルオロポリエーテル界面活性剤を用いるフッ素化モノマー類の水性乳化重合 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20100286330A1 (en) | 2010-11-11 |
| CN102428106A (zh) | 2012-04-25 |
| EP2427506A1 (en) | 2012-03-14 |
| EP2427506B1 (en) | 2013-08-14 |
| US8329813B2 (en) | 2012-12-11 |
| WO2010129842A1 (en) | 2010-11-11 |
| CN102428106B (zh) | 2014-08-13 |
| JP2014237842A (ja) | 2014-12-18 |
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