JP7116171B2 - フレキシブルコーティング用硬化性組成物 - Google Patents
フレキシブルコーティング用硬化性組成物 Download PDFInfo
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- JP7116171B2 JP7116171B2 JP2020528805A JP2020528805A JP7116171B2 JP 7116171 B2 JP7116171 B2 JP 7116171B2 JP 2020528805 A JP2020528805 A JP 2020528805A JP 2020528805 A JP2020528805 A JP 2020528805A JP 7116171 B2 JP7116171 B2 JP 7116171B2
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- Prior art keywords
- hard coat
- group
- oxyethylene
- film
- curable composition
- Prior art date
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- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 125000006356 alkylene carbonyl group Chemical group 0.000 description 2
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- 229910052799 carbon Inorganic materials 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
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- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
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- 238000005259 measurement Methods 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
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- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/062—Polyethers
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- 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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
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- 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
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
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- 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
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
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- 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
- C08F222/00—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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
-
- 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
- C08F222/00—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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- C08F222/103—Esters of polyhydric alcohols or polyhydric phenols of trialcohols, e.g. trimethylolpropane tri(meth)acrylate
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- 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
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Paints Or Removers (AREA)
- Laminated Bodies (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Polymerisation Methods In General (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Polyethers (AREA)
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| WO2020162326A1 (ja) * | 2019-02-06 | 2020-08-13 | 日産化学株式会社 | フレキシブルハードコート用硬化性組成物 |
| KR102868546B1 (ko) * | 2019-02-06 | 2025-10-13 | 닛산 가가쿠 가부시키가이샤 | 대전방지 하드코트용 경화성 조성물 |
| JP7332989B2 (ja) * | 2019-02-06 | 2023-08-24 | 日産化学株式会社 | 防眩性ハードコート用硬化性組成物 |
| WO2020162329A1 (ja) * | 2019-02-06 | 2020-08-13 | 日産化学株式会社 | ハードコート用硬化性組成物 |
| WO2020162322A1 (ja) * | 2019-02-06 | 2020-08-13 | 日産化学株式会社 | 耐光性ハードコート用硬化性組成物 |
| JP7587201B2 (ja) * | 2020-09-14 | 2024-11-20 | 日産化学株式会社 | 特定のウレタン（メタ）アクリレートを含むハードコート層形成用硬化性組成物 |
| JP7074825B1 (ja) | 2020-11-16 | 2022-05-24 | 株式会社ダイセル | 積層フィルム、及びフォルダブルデバイス |
| JP2022093249A (ja) * | 2020-12-11 | 2022-06-23 | 東亞合成株式会社 | 活性エネルギー線硬化型抗ウイルス用組成物 |
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Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005126453A (ja) | 2003-10-21 | 2005-05-19 | Tdk Corp | ハードコート剤組成物及びこれを用いた光情報媒体 |
| JP2009256597A (ja) | 2008-03-26 | 2009-11-05 | Jsr Corp | パーフルオロポリエーテル基、ウレタン基及び（メタ）アクリロイル基を有する化合物 |
| JP2013076029A (ja) | 2011-09-30 | 2013-04-25 | Tdk Corp | ハードコート剤組成物及びこれを用いたハードコートフィルム |
| JP2013163765A (ja) | 2012-02-10 | 2013-08-22 | Toyo Ink Sc Holdings Co Ltd | 活性エネルギー線硬化性組成物 |
| WO2013187528A1 (ja) | 2012-06-15 | 2013-12-19 | 三菱レイヨン株式会社 | 物品および活性エネルギー線硬化性樹脂組成物 |
| JP2015160902A (ja) | 2014-02-27 | 2015-09-07 | デクセリアルズ株式会社 | 表面調整剤及びそれを用いた物品 |
| WO2016163479A1 (ja) | 2015-04-07 | 2016-10-13 | 日産化学工業株式会社 | 耐擦傷性コーティング用硬化性組成物 |
| JP2017008128A (ja) | 2015-06-16 | 2017-01-12 | ユニマテック株式会社 | 活性エネルギー線硬化性樹脂組成物 |
| WO2018123463A1 (ja) | 2016-12-26 | 2018-07-05 | Dic株式会社 | 含フッ素活性エネルギー線硬化型樹脂、界面活性剤、活性エネルギー線硬化型樹脂組成物及び硬化塗膜 |
| WO2019045096A1 (ja) | 2017-09-01 | 2019-03-07 | 日産化学株式会社 | 延伸性耐擦傷性コーティング用硬化性組成物 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5098741B2 (ja) * | 2008-03-26 | 2012-12-12 | Ｊｓｒ株式会社 | ハードコート形成用硬化性組成物、硬化膜及び積層体 |
| JP5581943B2 (ja) | 2010-09-29 | 2014-09-03 | Ｄｉｃ株式会社 | 含フッ素重合性樹脂、活性エネルギー線硬化型塗料組成物及びその硬化物 |
| JP6203715B2 (ja) | 2012-06-22 | 2017-09-27 | ソマール株式会社 | エネルギー線硬化型樹脂組成物、硬化物及び積層体 |
| WO2015060458A1 (ja) * | 2013-10-25 | 2015-04-30 | 日産化学工業株式会社 | ヒドロキシ基を有するパーフルオロポリエーテルを含む重合性組成物 |
| CN109715685B (zh) * | 2016-09-21 | 2022-05-10 | 日产化学株式会社 | 耐擦伤性硬涂材 |
-
2019
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- 2019-06-24 WO PCT/JP2019/024994 patent/WO2020008937A1/ja not_active Ceased
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- 2019-07-02 TW TW108123197A patent/TWI791863B/zh active
-
2022
- 2022-07-27 JP JP2022119788A patent/JP7397412B2/ja active Active
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005126453A (ja) | 2003-10-21 | 2005-05-19 | Tdk Corp | ハードコート剤組成物及びこれを用いた光情報媒体 |
| JP2009256597A (ja) | 2008-03-26 | 2009-11-05 | Jsr Corp | パーフルオロポリエーテル基、ウレタン基及び（メタ）アクリロイル基を有する化合物 |
| JP2013076029A (ja) | 2011-09-30 | 2013-04-25 | Tdk Corp | ハードコート剤組成物及びこれを用いたハードコートフィルム |
| JP2013163765A (ja) | 2012-02-10 | 2013-08-22 | Toyo Ink Sc Holdings Co Ltd | 活性エネルギー線硬化性組成物 |
| WO2013187528A1 (ja) | 2012-06-15 | 2013-12-19 | 三菱レイヨン株式会社 | 物品および活性エネルギー線硬化性樹脂組成物 |
| JP2015160902A (ja) | 2014-02-27 | 2015-09-07 | デクセリアルズ株式会社 | 表面調整剤及びそれを用いた物品 |
| WO2016163479A1 (ja) | 2015-04-07 | 2016-10-13 | 日産化学工業株式会社 | 耐擦傷性コーティング用硬化性組成物 |
| JP2017008128A (ja) | 2015-06-16 | 2017-01-12 | ユニマテック株式会社 | 活性エネルギー線硬化性樹脂組成物 |
| WO2018123463A1 (ja) | 2016-12-26 | 2018-07-05 | Dic株式会社 | 含フッ素活性エネルギー線硬化型樹脂、界面活性剤、活性エネルギー線硬化型樹脂組成物及び硬化塗膜 |
| WO2019045096A1 (ja) | 2017-09-01 | 2019-03-07 | 日産化学株式会社 | 延伸性耐擦傷性コーティング用硬化性組成物 |
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| KR102791030B1 (ko) | 2025-04-07 |
| CN112368305B (zh) | 2023-03-28 |
| TWI791863B (zh) | 2023-02-11 |
| JP2022164666A (ja) | 2022-10-27 |
| JPWO2020008937A1 (ja) | 2021-08-05 |
| TW202016211A (zh) | 2020-05-01 |
| KR102547870B1 (ko) | 2023-06-27 |
| WO2020008937A1 (ja) | 2020-01-09 |
| JP7397412B2 (ja) | 2023-12-13 |
| CN112368305A (zh) | 2021-02-12 |
| KR20230093369A (ko) | 2023-06-27 |
| KR20210029768A (ko) | 2021-03-16 |
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