ES2547327T3 - Nuevos éteres de alquil-perfluoroalqueno y usos de los mismos - Google Patents
Nuevos éteres de alquil-perfluoroalqueno y usos de los mismos Download PDFInfo
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- ES2547327T3 ES2547327T3 ES10706080.8T ES10706080T ES2547327T3 ES 2547327 T3 ES2547327 T3 ES 2547327T3 ES 10706080 T ES10706080 T ES 10706080T ES 2547327 T3 ES2547327 T3 ES 2547327T3
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- 150000002170 ethers Chemical class 0.000 title description 28
- 125000000217 alkyl group Chemical group 0.000 title description 6
- 239000000203 mixture Substances 0.000 claims abstract description 157
- 229920001774 Perfluoroether Polymers 0.000 claims abstract description 16
- 239000002904 solvent Substances 0.000 claims description 82
- 238000004140 cleaning Methods 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 69
- 150000001875 compounds Chemical class 0.000 claims description 40
- 238000000576 coating method Methods 0.000 claims description 33
- 239000011248 coating agent Substances 0.000 claims description 28
- 238000000151 deposition Methods 0.000 claims description 16
- 238000009835 boiling Methods 0.000 claims description 11
- 238000005238 degreasing Methods 0.000 claims description 9
- 239000010702 perfluoropolyether Substances 0.000 claims description 6
- 239000003380 propellant Substances 0.000 claims description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 66
- 238000001035 drying Methods 0.000 description 52
- 239000000758 substrate Substances 0.000 description 51
- 239000003921 oil Substances 0.000 description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 40
- 238000006243 chemical reaction Methods 0.000 description 31
- -1 unsaturated fluorocarbon ethers Chemical class 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 27
- 239000004094 surface-active agent Substances 0.000 description 24
- 238000007792 addition Methods 0.000 description 19
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 17
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- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 15
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 15
- 238000007654 immersion Methods 0.000 description 14
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 230000004907 flux Effects 0.000 description 7
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 7
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- 150000003983 crown ethers Chemical class 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 6
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- 239000012530 fluid Substances 0.000 description 6
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- NISOCYUAQBTSBZ-UHFFFAOYSA-N n-methyl-n-(2-phenylethyl)prop-2-yn-1-amine Chemical compound C#CCN(C)CCC1=CC=CC=C1 NISOCYUAQBTSBZ-UHFFFAOYSA-N 0.000 description 6
- 230000008569 process Effects 0.000 description 6
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- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 5
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 5
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- 239000007864 aqueous solution Substances 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
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- 238000001816 cooling Methods 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical group [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
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- 229920001515 polyalkylene glycol Polymers 0.000 description 4
- 150000003242 quaternary ammonium salts Chemical group 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
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- UAEWLONMSWUOCA-UHFFFAOYSA-N 1,1,1,2,2,3,4,5,5,6,6,7,7,7-tetradecafluorohept-3-ene Chemical compound FC(F)(F)C(F)(F)C(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F UAEWLONMSWUOCA-UHFFFAOYSA-N 0.000 description 3
- RGBFMLVTZCWFSL-UHFFFAOYSA-N 1,1,1,2,3,4,4,5,5,6,6,7,7,8,8,8-hexadecafluorooct-2-ene Chemical compound FC(F)(F)C(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RGBFMLVTZCWFSL-UHFFFAOYSA-N 0.000 description 3
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 3
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 3
- CDAVUOSPHHTNBU-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5,6,6,7,7,7-tetradecafluorohept-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CDAVUOSPHHTNBU-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 241000283973 Oryctolagus cuniculus Species 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical class CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 150000004703 alkoxides Chemical class 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 210000005069 ears Anatomy 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 229920002120 photoresistant polymer Polymers 0.000 description 3
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- 238000005507 spraying Methods 0.000 description 3
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- VVMQLAKDFBLCHB-UHFFFAOYSA-N 1,1,1,2,3,4,4,5,5,5-decafluoropent-2-ene Chemical compound FC(F)(F)C(F)=C(F)C(F)(F)C(F)(F)F VVMQLAKDFBLCHB-UHFFFAOYSA-N 0.000 description 2
- RXTHCRMIJMEURB-UHFFFAOYSA-N 1,1,1,2,3,4,5,5,5-nonafluoro-4-methoxypent-2-ene Chemical compound COC(F)(C(F)(F)F)C(F)=C(F)C(F)(F)F RXTHCRMIJMEURB-UHFFFAOYSA-N 0.000 description 2
- GRAVXMKICSKBIS-UHFFFAOYSA-N 1,1,1,2,3,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-2-methoxyoct-3-ene Chemical compound COC(F)(C(F)(F)F)C(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F GRAVXMKICSKBIS-UHFFFAOYSA-N 0.000 description 2
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 2
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- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- AUFVJZSDSXXFOI-UHFFFAOYSA-N 2.2.2-cryptand Chemical compound C1COCCOCCN2CCOCCOCCN1CCOCCOCC2 AUFVJZSDSXXFOI-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 235000017399 Caesalpinia tinctoria Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
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- HMSWAIKSFDFLKN-UHFFFAOYSA-N Hexacosane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCC HMSWAIKSFDFLKN-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 206010025421 Macule Diseases 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
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- SYJPAKDNFZLSMV-HYXAFXHYSA-N (Z)-2-methylpropanal oxime Chemical compound CC(C)\C=N/O SYJPAKDNFZLSMV-HYXAFXHYSA-N 0.000 description 1
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- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 1
- IBWGNZVCJVLSHB-UHFFFAOYSA-M tetrabutylphosphanium;chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CCCC IBWGNZVCJVLSHB-UHFFFAOYSA-M 0.000 description 1
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- WAGFXJQAIZNSEQ-UHFFFAOYSA-M tetraphenylphosphonium chloride Chemical compound [Cl-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 WAGFXJQAIZNSEQ-UHFFFAOYSA-M 0.000 description 1
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- ADZJWYULTMTLQZ-UHFFFAOYSA-N tritylphosphane;hydrobromide Chemical compound [Br-].C=1C=CC=CC=1C(C=1C=CC=CC=1)([PH3+])C1=CC=CC=C1 ADZJWYULTMTLQZ-UHFFFAOYSA-N 0.000 description 1
- PPQRADLPLZYEKN-UHFFFAOYSA-N tritylphosphanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1C(C=1C=CC=CC=1)([PH3+])C1=CC=CC=C1 PPQRADLPLZYEKN-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C07C43/17—Unsaturated ethers containing halogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
-
- 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
- C07C43/164—Unsaturated ethers containing six-membered aromatic rings
- C07C43/166—Unsaturated ethers containing six-membered aromatic rings having unsaturation outside the aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5018—Halogenated solvents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Lubricants (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15280309P | 2009-02-16 | 2009-02-16 | |
| US152803P | 2009-02-16 | ||
| US28727509P | 2009-12-17 | 2009-12-17 | |
| US287275P | 2009-12-17 | ||
| PCT/US2010/024259 WO2010094019A2 (en) | 2009-02-16 | 2010-02-16 | Novel alkyl perfluoroalkene ethers and uses thereof |
Publications (1)
| Publication Number | Publication Date |
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| ES2547327T3 true ES2547327T3 (es) | 2015-10-05 |
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| ES10706080.8T Active ES2547327T3 (es) | 2009-02-16 | 2010-02-16 | Nuevos éteres de alquil-perfluoroalqueno y usos de los mismos |
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| EP (1) | EP2396294B1 (enExample) |
| JP (2) | JP2012518010A (enExample) |
| KR (1) | KR101856233B1 (enExample) |
| CN (1) | CN102317245B (enExample) |
| ES (1) | ES2547327T3 (enExample) |
| MY (1) | MY157701A (enExample) |
| SG (1) | SG173696A1 (enExample) |
| TW (1) | TWI418534B (enExample) |
| WO (1) | WO2010094019A2 (enExample) |
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| TW201226377A (en) * | 2010-12-20 | 2012-07-01 | Du Pont | Azeotropic and azeotrope-like compositions of methyl perfluoroheptene ethers and ethanol and uses thereof |
| JP6266983B2 (ja) * | 2011-03-10 | 2018-01-24 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | メチルパーフルオロヘプテンエーテルとトランス−１，２−ジクロロエチレンの共沸および共沸様組成物およびその使用 |
| US20130244922A1 (en) * | 2011-09-13 | 2013-09-19 | E I Du Pont De Nemours And Company | Azeotropic compositions comprising methyl perfluoropentene ethers for cleaning applications |
| JP2014530206A (ja) * | 2011-09-26 | 2014-11-17 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーＥ．Ｉ．Ｄｕ Ｐｏｎｔ Ｄｅ Ｎｅｍｏｕｒｓ Ａｎｄ Ｃｏｍｐａｎｙ | アルキルパーフルオロアルケンエーテル製造において成分を分離する方法 |
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| JP2013170256A (ja) * | 2012-02-22 | 2013-09-02 | Du Pont Mitsui Fluorochem Co Ltd | リンス剤およびリンス方法 |
| MX360992B (es) | 2012-09-14 | 2018-11-23 | Procter & Gamble | Composiciones antitranspirantes en aerosol, productos y metodos. |
| JP5995630B2 (ja) * | 2012-09-27 | 2016-09-21 | 三井・デュポンフロロケミカル株式会社 | 非晶質含フッ素樹脂組成物および薄膜製造方法 |
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| US11186424B2 (en) | 2013-07-16 | 2021-11-30 | The Procter & Gamble Company | Antiperspirant spray devices and compositions |
| US11083915B2 (en) | 2013-07-16 | 2021-08-10 | The Procter & Gamble Company | Antiperspirant spray devices and compositions |
| EP3024810B1 (en) | 2013-07-25 | 2018-06-20 | 3M Innovative Properties Company | Nitrogen containing hydrofluoroethers and methods of making same |
| US9909017B2 (en) * | 2013-11-01 | 2018-03-06 | Zyp Coatings, Inc. | Miscible solvent system and method for making same |
| US9579265B2 (en) | 2014-03-13 | 2017-02-28 | The Procter & Gamble Company | Aerosol antiperspirant compositions, products and methods |
| US9662285B2 (en) | 2014-03-13 | 2017-05-30 | The Procter & Gamble Company | Aerosol antiperspirant compositions, products and methods |
| EP3143118B1 (en) | 2014-05-13 | 2018-10-10 | The Chemours Company FC, LLC | Compositions of methyl perfluoroheptene ethers, 1,1,1,2,2,3,4,5,5,5-decafluoropentane and trans-1,2-dichloroethylene and uses thereof |
| KR102411949B1 (ko) | 2014-07-16 | 2022-06-22 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 하이드로플루오로에테르 올레핀 및 이의 사용 방법 |
| US9840685B2 (en) | 2015-05-08 | 2017-12-12 | The Chemours Company Fc, Llc | Ternary compositions of methyl perfluoroheptene ethers and trans-1,2-dichloroethylene, and uses thereof |
| JP7202082B2 (ja) | 2017-06-23 | 2023-01-11 | 三井・ケマーズ フロロプロダクツ株式会社 | 熱溶融性フッ素樹脂成形品 |
| WO2018237297A1 (en) | 2017-06-23 | 2018-12-27 | Dupont-Mitsui Fluorochemicals Co. Ltd | Melt processible fluororesin molded article |
| CN107602866B (zh) * | 2017-08-28 | 2021-01-12 | 无锡龙驰氟硅新材料有限公司 | 一种氟硅表面活性剂及其制备方法 |
| US11124744B2 (en) | 2017-10-20 | 2021-09-21 | Shellef Holdings Inc. | Compositions containing trans-1,2-dichloroethylene and a hydrofluoroether, and methods of using the same |
| WO2019093350A1 (ja) * | 2017-11-07 | 2019-05-16 | 神戸合成株式会社 | 洗浄剤組成物及びそのエアゾール組成物 |
| JP7086104B2 (ja) * | 2017-12-07 | 2022-06-17 | 関東電化工業株式会社 | 塩素化ビス（３，３，３－トリフルオロ－１－プロペニル）エーテル、その製造方法及びその用途 |
| US11898124B2 (en) * | 2018-04-27 | 2024-02-13 | Threebond Co., Ltd. | Cleaner composition, cleaning aerosol, and method for cleaning contaminated part |
| JP7525481B2 (ja) * | 2018-10-15 | 2024-07-30 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | フッ素化アルコキシビニルエーテル及びフッ素化アルコキシビニルエーテルの調製方法 |
| WO2020136533A1 (en) * | 2018-12-26 | 2020-07-02 | 3M Innovative Properties Company | Hydrochlorofluoroolefins and methods of using same |
| ES3048489T3 (en) * | 2019-10-28 | 2025-12-10 | Chemours Co Fc Llc | Heat transfer fluids for use in low temperature chiller applications |
| TWI879951B (zh) * | 2020-05-19 | 2025-04-11 | 美商科慕Ｆｃ有限責任公司 | 穩定化熱傳流體組成物 |
| JP7643843B2 (ja) | 2020-08-03 | 2025-03-11 | 三井・ケマーズ フロロプロダクツ株式会社 | 樹脂ペレット及びその成形品 |
| US20230323180A1 (en) * | 2020-08-28 | 2023-10-12 | Solvay Specialty Polymers Italy S.P.A. | Heat exchange method using fluorinated vinylethers having a low gwp |
| US20240021889A1 (en) * | 2020-12-11 | 2024-01-18 | Mexichem Fluor S.A. De C.V. | Composition |
| CN119775111A (zh) * | 2025-01-03 | 2025-04-08 | 超聚变数字技术有限公司 | 一种氢氟烯醚类化合物及其制备方法和应用 |
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| NL121693C (enExample) | 1959-05-22 | |||
| JPS58146567A (ja) | 1982-02-25 | 1983-09-01 | Agency Of Ind Science & Technol | イオノフオアとして有用なポリエ−テル誘導体 |
| DE3338300A1 (de) * | 1983-10-21 | 1985-05-02 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von fluoralkylsubstituierten iod-alkanen |
| GB8924057D0 (en) * | 1989-10-25 | 1989-12-13 | Ici Plc | Lubricants |
| US5171902A (en) * | 1990-10-11 | 1992-12-15 | E. I. Du Pont De Nemours And Company | Saturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions |
| US6008179A (en) | 1995-05-16 | 1999-12-28 | 3M Innovative Properties Company | Azeotrope-like compositions and their use |
| US6030934A (en) * | 1997-02-19 | 2000-02-29 | 3M Innovative Properties Company | Azeotropic compositions of methoxy-perfluoropropane and their use |
| US5908822A (en) | 1997-10-28 | 1999-06-01 | E. I. Du Pont De Nemours And Company | Compositions and processes for drying substrates |
| US6849194B2 (en) | 2000-11-17 | 2005-02-01 | Pcbu Services, Inc. | Methods for preparing ethers, ether compositions, fluoroether fire extinguishing systems, mixtures and methods |
| JP2002338631A (ja) * | 2001-03-14 | 2002-11-27 | Asahi Glass Co Ltd | テトラフルオロエチレン重合体の製造方法 |
| US7071154B2 (en) * | 2003-12-18 | 2006-07-04 | 3M Innovative Properties Company | Azeotrope-like compositions and their use |
| US20060122301A1 (en) * | 2004-12-08 | 2006-06-08 | Honeywell International Inc. | Fluorinated divinyl ethers |
| JP4772387B2 (ja) * | 2005-06-08 | 2011-09-14 | 株式会社ネオス | ノニオン系含フッ素界面活性剤及びその製造方法 |
| JP2007039376A (ja) * | 2005-08-03 | 2007-02-15 | Central Glass Co Ltd | ハイドロフルオロエーテルの製造方法 |
| US7691282B2 (en) * | 2005-09-08 | 2010-04-06 | 3M Innovative Properties Company | Hydrofluoroether compounds and processes for their preparation and use |
| JP4786983B2 (ja) * | 2005-09-21 | 2011-10-05 | 株式会社ネオス | 含フッ素ポリエーテル |
| MY145459A (en) * | 2005-11-01 | 2012-02-15 | Du Pont | Solvent compositions comprising unsaturated fluorinated hydrocarbons |
| US7708903B2 (en) * | 2005-11-01 | 2010-05-04 | E.I. Du Pont De Nemours And Company | Compositions comprising fluoroolefins and uses thereof |
| KR20080114757A (ko) * | 2006-02-28 | 2008-12-31 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 세정 분야를 위한 플루오르화 화합물을 포함하는 공비 조성물 |
| US20080008019A1 (en) | 2006-07-06 | 2008-01-10 | Texas Instruments Incorporated | High Speed Read-Only Memory |
| US8486295B2 (en) * | 2010-07-09 | 2013-07-16 | E I Du Pont De Nemours And Company | Alkyl perfluoroalkene ethers and uses thereof |
-
2010
- 2010-02-08 US US12/701,802 patent/US8399713B2/en active Active
- 2010-02-16 CN CN201080007905.1A patent/CN102317245B/zh active Active
- 2010-02-16 MY MYPI2011003315A patent/MY157701A/en unknown
- 2010-02-16 KR KR1020117021475A patent/KR101856233B1/ko active Active
- 2010-02-16 JP JP2011550306A patent/JP2012518010A/ja active Pending
- 2010-02-16 EP EP10706080.8A patent/EP2396294B1/en active Active
- 2010-02-16 SG SG2011058591A patent/SG173696A1/en unknown
- 2010-02-16 WO PCT/US2010/024259 patent/WO2010094019A2/en not_active Ceased
- 2010-02-16 ES ES10706080.8T patent/ES2547327T3/es active Active
- 2010-02-22 TW TW099105027A patent/TWI418534B/zh active
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2011
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2015
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Also Published As
| Publication number | Publication date |
|---|---|
| MY157701A (en) | 2016-07-15 |
| US8399713B2 (en) | 2013-03-19 |
| WO2010094019A3 (en) | 2011-02-17 |
| TW201100367A (en) | 2011-01-01 |
| US20100209600A1 (en) | 2010-08-19 |
| SG173696A1 (en) | 2011-09-29 |
| HK1165786A1 (en) | 2012-10-12 |
| CN102317245A (zh) | 2012-01-11 |
| KR101856233B1 (ko) | 2018-06-25 |
| CN102317245B (zh) | 2015-06-17 |
| JP5881875B2 (ja) | 2016-03-09 |
| EP2396294B1 (en) | 2015-07-22 |
| US20110282104A1 (en) | 2011-11-17 |
| KR20110121635A (ko) | 2011-11-07 |
| JP2012518010A (ja) | 2012-08-09 |
| WO2010094019A2 (en) | 2010-08-19 |
| EP2396294A2 (en) | 2011-12-21 |
| TWI418534B (zh) | 2013-12-11 |
| JP2015110802A (ja) | 2015-06-18 |
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