CN104945611B - 含有氟聚醚的聚合物 - Google Patents
含有氟聚醚的聚合物 Download PDFInfo
- Publication number
- CN104945611B CN104945611B CN201510147606.2A CN201510147606A CN104945611B CN 104945611 B CN104945611 B CN 104945611B CN 201510147606 A CN201510147606 A CN 201510147606A CN 104945611 B CN104945611 B CN 104945611B
- Authority
- CN
- China
- Prior art keywords
- polymer
- perfluoroalkyl polyether
- fluoro
- polymer containing
- containing perfluoroalkyl
- 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.)
- Active
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 55
- 125000005010 perfluoroalkyl group Chemical group 0.000 title claims abstract description 26
- 229920000570 polyether Polymers 0.000 title claims abstract description 26
- 239000004721 Polyphenylene oxide Substances 0.000 title claims abstract description 25
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 230000003252 repetitive effect Effects 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 9
- 230000004048 modification Effects 0.000 abstract description 8
- 238000012986 modification Methods 0.000 abstract description 8
- 229910000077 silane Inorganic materials 0.000 abstract description 8
- 239000005871 repellent Substances 0.000 abstract 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 17
- 229910052731 fluorine Inorganic materials 0.000 description 17
- 239000011737 fluorine Substances 0.000 description 17
- 239000002904 solvent Substances 0.000 description 16
- -1 siloxanes Chemical class 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 239000003153 chemical reaction reagent Substances 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- RMRFFCXPLWYOOY-UHFFFAOYSA-N allyl radical Chemical compound [CH2]C=C RMRFFCXPLWYOOY-UHFFFAOYSA-N 0.000 description 9
- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
- 150000002222 fluorine compounds Chemical class 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 229910052749 magnesium Inorganic materials 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 150000001721 carbon Chemical group 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 3
- 125000005370 alkoxysilyl group Chemical group 0.000 description 3
- 125000001118 alkylidene group Chemical group 0.000 description 3
- 125000000746 allylic group Chemical group 0.000 description 3
- 230000031709 bromination Effects 0.000 description 3
- 238000005893 bromination reaction Methods 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 239000004519 grease Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000005702 oxyalkylene group Chemical group 0.000 description 3
- 239000013557 residual solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- PZHIWRCQKBBTOW-UHFFFAOYSA-N 1-ethoxybutane Chemical compound CCCCOCC PZHIWRCQKBBTOW-UHFFFAOYSA-N 0.000 description 2
- FNUBKINEQIEODM-UHFFFAOYSA-N 3,3,4,4,5,5,5-heptafluoropentanal Chemical compound FC(F)(F)C(F)(F)C(F)(F)CC=O FNUBKINEQIEODM-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- LEUZQDVZEOKCCV-UHFFFAOYSA-N N=NC=NN.N=NC=NN.C(COCCOCCOCCO)O Chemical compound N=NC=NN.N=NC=NN.C(COCCOCCOCCO)O LEUZQDVZEOKCCV-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000026030 halogenation Effects 0.000 description 2
- 238000005658 halogenation reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000005647 linker group Chemical group 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical group CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- ZPFKRQXYKULZKP-UHFFFAOYSA-N butylidene Chemical group [CH2+]CC[CH-] ZPFKRQXYKULZKP-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003682 fluorination reaction Methods 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002939 oilproofing Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/002—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds
- C08G65/005—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/002—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds
- C08G65/005—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens
- C08G65/007—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
- C08G65/3322—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterized by the type of post-polymerisation functionalisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/46—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing halogen
- C08G2650/48—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing halogen containing fluorine, e.g. perfluropolyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyethers (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2014074126A JP6119656B2 (ja) | 2014-03-31 | 2014-03-31 | フルオロポリエーテル基含有ポリマー |
| JP2014-074126 | 2014-03-31 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104945611A CN104945611A (zh) | 2015-09-30 |
| CN104945611B true CN104945611B (zh) | 2018-11-02 |
Family
ID=52726991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510147606.2A Active CN104945611B (zh) | 2014-03-31 | 2015-03-31 | 含有氟聚醚的聚合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9534082B2 (enExample) |
| EP (1) | EP2927261B1 (enExample) |
| JP (1) | JP6119656B2 (enExample) |
| KR (1) | KR102244788B1 (enExample) |
| CN (1) | CN104945611B (enExample) |
| TW (1) | TWI656144B (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3085749B1 (en) * | 2015-04-20 | 2017-06-28 | Shin-Etsu Chemical Co., Ltd. | Fluoropolyether-containing polymer-modified silane, surface treating agent, and treated article |
| JP6260579B2 (ja) * | 2015-05-01 | 2018-01-17 | 信越化学工業株式会社 | フルオロポリエーテル基含有ポリマー変性シラン、表面処理剤及び物品 |
| WO2017077833A1 (ja) * | 2015-11-06 | 2017-05-11 | 信越化学工業株式会社 | 表面処理された樹脂製品 |
| JP6521091B2 (ja) * | 2015-11-06 | 2019-05-29 | 信越化学工業株式会社 | フルオロポリエーテル基含有ポリマー変性有機ケイ素化合物、表面処理剤及び物品 |
| KR102648009B1 (ko) * | 2015-12-14 | 2024-03-18 | 신에쓰 가가꾸 고교 가부시끼가이샤 | 플루오로폴리에터기 함유 폴리머 변성 실레인, 표면처리제 및 물품 |
| EP3508513B1 (en) | 2016-08-30 | 2022-11-23 | Agc Inc. | Processes for producing fluorinated ether compounds |
| WO2019044479A1 (ja) * | 2017-08-31 | 2019-03-07 | Ａｇｃ株式会社 | 含フッ素エーテル化合物、含フッ素エーテル組成物、コーティング液、物品およびその製造方法 |
| EP3981823A4 (en) * | 2019-06-06 | 2022-12-28 | Shin-Etsu Chemical Co., Ltd. | POLYMER CONTAINING FLUOROPOLYETHER GROUP AND METHOD FOR PRODUCTION |
| CN118725281A (zh) * | 2019-09-26 | 2024-10-01 | 大金工业株式会社 | 含氟代聚醚基化合物 |
| KR20220151662A (ko) | 2020-03-09 | 2022-11-15 | 에이지씨 가부시키가이샤 | 함불소 에테르 화합물 및 그 제조 방법, 화합물 및 그 제조 방법, 함불소 에테르 조성물, 코팅액, 그리고 물품 및 그 제조 방법 |
| WO2022209674A1 (ja) * | 2021-03-30 | 2022-10-06 | ダイキン工業株式会社 | フルオロポリエーテル基含有シラン化合物 |
| CN120322485A (zh) * | 2022-12-09 | 2025-07-15 | 信越化学工业株式会社 | 含有氟聚醚基的聚合物、表面处理剂和物品 |
| WO2024247807A1 (ja) * | 2023-06-01 | 2024-12-05 | 信越化学工業株式会社 | フルオロポリエーテル基含有ポリマー及びその製造方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102558877A (zh) * | 2010-09-28 | 2012-07-11 | 信越化学工业株式会社 | 含氟氧基亚烷基聚合物组成物及含该组成物的表面处理剂、及由该表面处理剂进行表面处理的物品 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1632516B1 (en) * | 2000-07-19 | 2008-04-02 | E.I.Du pont de nemours and company | Perfluoropolyethers and processes therefor and therewith |
| JP2005200481A (ja) * | 2004-01-13 | 2005-07-28 | Shin Etsu Chem Co Ltd | 射出成型用フルオロポリエーテルゴム組成物 |
| JP5747699B2 (ja) * | 2011-07-12 | 2015-07-15 | 信越化学工業株式会社 | フルオロオキシアルキレン基含有ポリマー変性シラン及び該シランを含む表面処理剤並びに該表面処理剤で表面処理された物品 |
| EP2756024B1 (en) * | 2011-10-03 | 2015-11-18 | Solvay Specialty Polymers Italy S.p.A. | Linear (per)fluoropolyethers with -cf(cf3)cof end groups and derivatives thereof |
| KR102016195B1 (ko) * | 2012-02-17 | 2019-08-29 | 에이지씨 가부시키가이샤 | 함불소 에테르 화합물, 함불소 에테르 조성물 및 코팅액, 그리고 표면 처리층을 갖는 기재 및 그 제조 방법 |
| JP2014074126A (ja) | 2012-10-05 | 2014-04-24 | Toray Ind Inc | フィルム |
| JP6451279B2 (ja) * | 2014-03-31 | 2019-01-16 | 信越化学工業株式会社 | フルオロポリエーテル基含有ポリマー変性シラン、表面処理剤及び物品 |
-
2014
- 2014-03-31 JP JP2014074126A patent/JP6119656B2/ja active Active
-
2015
- 2015-03-18 EP EP15159694.7A patent/EP2927261B1/en active Active
- 2015-03-25 US US14/668,223 patent/US9534082B2/en active Active
- 2015-03-26 KR KR1020150042342A patent/KR102244788B1/ko active Active
- 2015-03-30 TW TW104110251A patent/TWI656144B/zh active
- 2015-03-31 CN CN201510147606.2A patent/CN104945611B/zh active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102558877A (zh) * | 2010-09-28 | 2012-07-11 | 信越化学工业株式会社 | 含氟氧基亚烷基聚合物组成物及含该组成物的表面处理剂、及由该表面处理剂进行表面处理的物品 |
Non-Patent Citations (1)
| Title |
|---|
| SHEVELEVA, E.E.,etal..SYNTHESIS OF POLYMERS OF 4-HYDROXY-4-PERFLUOROALKYL-1,6-DIENES UNDER HIGH-PRESSURE.《Zhurnal organicheskoĭkhimii》.1994,第30卷(第8期),第1256-1258页. * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20150274888A1 (en) | 2015-10-01 |
| KR20150113880A (ko) | 2015-10-08 |
| TWI656144B (zh) | 2019-04-11 |
| EP2927261A1 (en) | 2015-10-07 |
| KR102244788B1 (ko) | 2021-04-28 |
| TW201605930A (zh) | 2016-02-16 |
| US9534082B2 (en) | 2017-01-03 |
| EP2927261B1 (en) | 2017-02-08 |
| CN104945611A (zh) | 2015-09-30 |
| JP2015196723A (ja) | 2015-11-09 |
| JP6119656B2 (ja) | 2017-04-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104945611B (zh) | 含有氟聚醚的聚合物 | |
| KR102526826B1 (ko) | 함불소 에테르 조성물, 코팅액 및 물품 | |
| KR101685266B1 (ko) | 불소 함유 공중합체, 및 발유성 및/또는 발수성 코팅제 | |
| KR20180044282A (ko) | 함불소 에테르 화합물, 함불소 에테르 조성물, 코팅액 및 물품 | |
| JP7056462B2 (ja) | 含フッ素エーテル化合物、含フッ素エーテル組成物、コーティング液、物品およびその製造方法 | |
| KR102531226B1 (ko) | 함불소 에테르 조성물, 코팅액 및 물품 | |
| JP7180665B2 (ja) | 含フッ素エーテル化合物、含フッ素エーテル組成物、コーティング液、物品及びその製造方法 | |
| JPWO2019049753A1 (ja) | 含フッ素エーテル化合物、組成物および物品 | |
| KR20150138179A (ko) | 함불소 에테르 화합물, 함불소 에테르 조성물 및 코팅액, 그리고 표면층을 갖는 기재 및 그 제조 방법 | |
| KR20160129829A (ko) | 함불소 에테르 조성물, 그 제조 방법, 코팅액, 표면 처리층을 갖는 기재 및 그 제조 방법 | |
| KR102869124B1 (ko) | 함불소 에테르 조성물, 코팅액, 물품 및 그 제조 방법 | |
| EP1127935B1 (en) | Fluorine-containing surface treatment composition | |
| JPWO2019208503A1 (ja) | 含フッ素エーテル化合物、それを含む組成物、コーティング液及び物品 | |
| EP3981823A1 (en) | Fluoropolyether group-containing polymer and production method therefor | |
| CN114957646B (zh) | 一种全氟聚醚胺基化合物及其制备方法与应用 | |
| KR20150130237A (ko) | 함불소 코팅제 및 이 코팅제로 처리된 물품 | |
| JP6993894B2 (ja) | 組成物 | |
| JP6587040B2 (ja) | 蒸着用含フッ素エーテル組成物、ならびに蒸着膜付き物品およびその製造方法 | |
| EP4265413A1 (en) | Surface treatment agent and article treated with said surface treatment agent |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |