KR20170116113A - 아이소시아네이트-유도된 (메트)아크릴레이트-함유 중합체성 화합물을 포함하는 불소-무함유 조성물을 사용하여 섬유질 기재를 처리하는 방법 - Google Patents
아이소시아네이트-유도된 (메트)아크릴레이트-함유 중합체성 화합물을 포함하는 불소-무함유 조성물을 사용하여 섬유질 기재를 처리하는 방법 Download PDFInfo
- Publication number
- KR20170116113A KR20170116113A KR1020177025319A KR20177025319A KR20170116113A KR 20170116113 A KR20170116113 A KR 20170116113A KR 1020177025319 A KR1020177025319 A KR 1020177025319A KR 20177025319 A KR20177025319 A KR 20177025319A KR 20170116113 A KR20170116113 A KR 20170116113A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- meth
- acrylate
- carbon atoms
- derived
- 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.)
- Withdrawn
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title claims abstract description 89
- 239000000203 mixture Substances 0.000 title claims abstract description 68
- 238000000034 method Methods 0.000 title claims abstract description 64
- 229920000642 polymer Polymers 0.000 title claims abstract description 62
- 239000000758 substrate Substances 0.000 title claims abstract description 44
- 239000012948 isocyanate Substances 0.000 title claims abstract description 31
- 150000002513 isocyanates Chemical class 0.000 title claims abstract description 30
- 230000008569 process Effects 0.000 title description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 99
- 239000000178 monomer Substances 0.000 claims abstract description 46
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 39
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 28
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 8
- -1 carpet Substances 0.000 claims description 32
- 125000002947 alkylene group Chemical group 0.000 claims description 26
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 15
- 239000004744 fabric Substances 0.000 claims description 14
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- 239000003054 catalyst Substances 0.000 description 4
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
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- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- VHIZYFAEPDWBFM-UHFFFAOYSA-M bis(2-hexadecanoyloxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC(=O)OCC[N+](C)(C)CCOC(=O)CCCCCCCCCCCCCCC VHIZYFAEPDWBFM-UHFFFAOYSA-M 0.000 description 1
- NSPSPMKCKIPQBH-UHFFFAOYSA-K bismuth;7,7-dimethyloctanoate Chemical compound [Bi+3].CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O NSPSPMKCKIPQBH-UHFFFAOYSA-K 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- UJGLEDCKGRRXHS-UHFFFAOYSA-N dioctadecyl 2-methylidenebutanedioate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CC(=C)C(=O)OCCCCCCCCCCCCCCCCCC UJGLEDCKGRRXHS-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- MJEMIOXXNCZZFK-UHFFFAOYSA-N ethylone Chemical compound CCNC(C)C(=O)C1=CC=C2OCOC2=C1 MJEMIOXXNCZZFK-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 1
- WHIVNJATOVLWBW-SNAWJCMRSA-N methylethyl ketone oxime Chemical compound CC\C(C)=N\O WHIVNJATOVLWBW-SNAWJCMRSA-N 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Polymers CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- ROEHNQZQCCPZCH-UHFFFAOYSA-N tert-butyl 2-tert-butylperoxycarbonylbenzoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1C(=O)OC(C)(C)C ROEHNQZQCCPZCH-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical group CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/267—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
-
- 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
- C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F120/10—Esters
- C08F120/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F120/36—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate containing oxygen in addition to the carboxy oxygen, e.g. 2-N-morpholinoethyl (meth)acrylate or 2-isocyanatoethyl (meth)acrylate
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F20/36—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate containing oxygen in addition to the carboxy oxygen, e.g. 2-N-morpholinoethyl (meth)acrylate or 2-isocyanatoethyl (meth)acrylate
-
- 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
- C08F214/02—Monomers containing chlorine
- C08F214/04—Monomers containing two carbon atoms
- C08F214/08—Vinylidene chloride
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F220/343—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F220/36—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate containing oxygen in addition to the carboxy oxygen, e.g. 2-N-morpholinoethyl (meth)acrylate or 2-isocyanatoethyl (meth)acrylate
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/12—Hydrophobic properties
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562115937P | 2015-02-13 | 2015-02-13 | |
| US62/115,937 | 2015-02-13 | ||
| PCT/US2016/016713 WO2016130415A1 (en) | 2015-02-13 | 2016-02-05 | Methods for treating fibrous substrates using fluorine-free compositions including isocyanate-derived (meth)acrylate-containing polymeric compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20170116113A true KR20170116113A (ko) | 2017-10-18 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020177025319A Withdrawn KR20170116113A (ko) | 2015-02-13 | 2016-02-05 | 아이소시아네이트-유도된 (메트)아크릴레이트-함유 중합체성 화합물을 포함하는 불소-무함유 조성물을 사용하여 섬유질 기재를 처리하는 방법 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20180016739A1 (OSRAM) |
| EP (1) | EP3256638B1 (OSRAM) |
| JP (1) | JP6932081B2 (OSRAM) |
| KR (1) | KR20170116113A (OSRAM) |
| CN (1) | CN107407047B (OSRAM) |
| BR (1) | BR112017016891A2 (OSRAM) |
| TW (1) | TWI684692B (OSRAM) |
| WO (1) | WO2016130415A1 (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102018117119A1 (de) | 2017-09-11 | 2019-03-14 | Samsung Electronics Co., Ltd. | Betriebsverfahren von nichtflüchtigen Speichervorrichtungen und Betriebsverfahren von Speichersteuerungen |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016130503A1 (en) | 2015-02-13 | 2016-08-18 | 3M Innovative Properties Company | Fluorine-free fibrous treating compositions including isocyanate- derived ethylenically unsaturated monomer-containing oligomers, and treating methods |
| JP6735763B2 (ja) | 2015-02-13 | 2020-08-05 | スリーエム イノベイティブ プロパティズ カンパニー | ポリカルボジイミド及び任意にパラフィンワックスを含むフッ素不含繊維処理組成物、並びに処理方法 |
| CA2989690A1 (en) | 2015-06-17 | 2016-12-22 | Clariant International Ltd | Water-soluble or water-swellable polymers as water loss reducers in cement slurries |
| JP6987847B2 (ja) | 2016-08-12 | 2022-01-05 | スリーエム イノベイティブ プロパティズ カンパニー | フッ素非含有繊維処理組成物、処理された基材、及び処理方法 |
| CN110300573B (zh) | 2016-12-12 | 2023-07-25 | 科莱恩国际有限公司 | 生物基聚合物在化妆、皮肤病学或药物学组合物中的用途 |
| EP3551680A1 (en) | 2016-12-12 | 2019-10-16 | Clariant International Ltd | Polymer comprising certain level of bio-based carbon |
| EP3554646B1 (en) | 2016-12-15 | 2025-03-19 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| EP3554643B1 (en) | 2016-12-15 | 2025-03-19 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| WO2018108663A1 (en) | 2016-12-15 | 2018-06-21 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| ES3032643T3 (en) | 2016-12-15 | 2025-07-22 | Clariant Int Ltd | Water-soluble and/or water-swellable hybrid polymer |
| KR101962816B1 (ko) * | 2017-06-14 | 2019-03-27 | (주)대동켐텍 | 폴리아크릴계 표면 발수제 및 그를 이용한 발수성 섬유제품 |
| CN111417753A (zh) * | 2017-11-30 | 2020-07-14 | 3M创新有限公司 | 组合物、处理方法和经处理的纤维基底 |
| EP3757187A4 (en) | 2018-02-20 | 2021-10-27 | Daikin Industries, Ltd. | SURFACE TREATMENT AGENT |
| CN109112835A (zh) * | 2018-07-19 | 2019-01-01 | 上海应用技术大学 | 一种与氟系防水剂同浴使用的阳离子硬挺剂及其制备方法 |
| CN108951172B (zh) * | 2018-07-19 | 2021-05-11 | 上海应用技术大学 | 一种与氟系防水剂同浴使用的有机硅柔软剂及其制备方法 |
| EP4317213A4 (en) * | 2021-03-31 | 2025-04-02 | Daikin Industries, Ltd. | Oil-resistant compound containing hydrogen binding site |
| CN119278243A (zh) | 2022-06-02 | 2025-01-07 | 明成化学工业株式会社 | 耐油剂组合物及耐油制品 |
| WO2025249398A1 (ja) * | 2024-05-31 | 2025-12-04 | 株式会社レゾナック | 活性エネルギー線硬化性撥水撥油剤組成物及び撥水撥油基材 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1455905A (fr) * | 1964-05-28 | 1966-10-21 | Nouvelles méthodes pour le traitement des matières fibreuses ainsi que produits obtenus | |
| JPS6024828B2 (ja) * | 1979-08-24 | 1985-06-14 | 積水化学工業株式会社 | 剥離剤 |
| CA2037319A1 (en) * | 1990-03-21 | 1991-09-22 | Chi-Ming Tseng | Water-borne acrylic low adhesion backsize and release coating compositions, methods of making the compositions, and sheet materials coated therewith |
| CN1113913C (zh) * | 1996-06-13 | 2003-07-09 | 大金工业株式会社 | 新型共聚物及其制造方法和用途 |
| US6197378B1 (en) * | 1997-05-05 | 2001-03-06 | 3M Innovative Properties Company | Treatment of fibrous substrates to impart repellency, stain resistance, and soil resistance |
| JP2000129573A (ja) * | 1998-10-23 | 2000-05-09 | Unitika Ltd | 防水性セルロース系繊維布帛およびその製造方法 |
| BRPI0418241A (pt) * | 2003-12-31 | 2007-04-17 | 3M Innovative Properties Co | fluoroacrilato, isocianato fluorado, polìmero acrìlico fluorado, composição de revestimento, e, artigo |
| CN103469904A (zh) * | 2007-12-21 | 2013-12-25 | 3M创新有限公司 | 密封表面的方法 |
| EP2302130A1 (de) * | 2009-09-26 | 2011-03-30 | Huntsman Textile Effects (Germany) GmbH | Zusammensetzung für die Öl- und/oder Wasserabweisende Ausrüstung von Fasermaterialien |
| WO2013162704A1 (en) | 2012-04-24 | 2013-10-31 | 3M Innovative Properties Company | Fluorochemical compounds, compositions, articles, and methods |
| CN104059518A (zh) * | 2014-01-13 | 2014-09-24 | 江苏苏博特新材料股份有限公司 | 一种环保型高性能甲基丙烯酸甲酯自流平涂料及其制备方法与应用 |
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2016
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- 2016-02-05 EP EP16709844.1A patent/EP3256638B1/en active Active
- 2016-02-05 WO PCT/US2016/016713 patent/WO2016130415A1/en not_active Ceased
- 2016-02-05 JP JP2017542144A patent/JP6932081B2/ja active Active
- 2016-02-05 US US15/547,932 patent/US20180016739A1/en not_active Abandoned
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- 2016-02-05 CN CN201680009453.8A patent/CN107407047B/zh active Active
- 2016-02-15 TW TW105104336A patent/TWI684692B/zh active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102018117119A1 (de) | 2017-09-11 | 2019-03-14 | Samsung Electronics Co., Ltd. | Betriebsverfahren von nichtflüchtigen Speichervorrichtungen und Betriebsverfahren von Speichersteuerungen |
Also Published As
| Publication number | Publication date |
|---|---|
| EP3256638A1 (en) | 2017-12-20 |
| TW201704589A (zh) | 2017-02-01 |
| WO2016130415A1 (en) | 2016-08-18 |
| EP3256638B1 (en) | 2022-01-19 |
| US20180016739A1 (en) | 2018-01-18 |
| JP6932081B2 (ja) | 2021-09-08 |
| TWI684692B (zh) | 2020-02-11 |
| BR112017016891A2 (pt) | 2018-03-27 |
| CN107407047B (zh) | 2020-10-27 |
| CN107407047A (zh) | 2017-11-28 |
| JP2018506657A (ja) | 2018-03-08 |
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