WO2017138544A1 - 透明両面粘着シート及び粘着シート積層体 - Google Patents
透明両面粘着シート及び粘着シート積層体 Download PDFInfo
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- WO2017138544A1 WO2017138544A1 PCT/JP2017/004489 JP2017004489W WO2017138544A1 WO 2017138544 A1 WO2017138544 A1 WO 2017138544A1 JP 2017004489 W JP2017004489 W JP 2017004489W WO 2017138544 A1 WO2017138544 A1 WO 2017138544A1
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- meth
- adhesive sheet
- sensitive adhesive
- image display
- pressure
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- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000003685 thermal hair damage Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/10—Adhesives in the form of films or foils without carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
- C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
-
- 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
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- 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
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
-
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/132—Phenols containing keto groups, e.g. benzophenones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives 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
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/06—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/385—Acrylic polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/40—Adhesives in the form of films or foils characterised by release liners
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
- G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
- G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
- G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
- C09J2301/124—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present on both sides of the carrier, e.g. double-sided adhesive tape
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/312—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
- C09J2301/416—Additional features of adhesives in the form of films or foils characterized by the presence of essential components use of irradiation
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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KR1020247002880A KR20240017413A (ko) | 2016-02-08 | 2017-02-08 | 투명 양면 점착 시트 및 점착 시트 적층체 |
KR1020187025929A KR102652894B1 (ko) | 2016-02-08 | 2017-02-08 | 투명 양면 점착 시트 및 점착 시트 적층체 |
CN201780010541.4A CN108699405B (zh) | 2016-02-08 | 2017-02-08 | 透明两面粘合片及粘合片层叠体 |
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
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JP2016-022113 | 2016-02-08 | ||
JP2016022113 | 2016-02-08 | ||
JP2016038166 | 2016-02-29 | ||
JP2016-038166 | 2016-02-29 | ||
JP2016-057812 | 2016-03-23 | ||
JP2016057812A JP6558287B2 (ja) | 2016-03-23 | 2016-03-23 | 画像表示装置構成用積層体及び画像表示装置の製造方法 |
JP2016-227505 | 2016-11-24 | ||
JP2016227505A JP7197255B2 (ja) | 2016-02-29 | 2016-11-24 | 透明両面粘着シート及び粘着シート積層体 |
Publications (1)
Publication Number | Publication Date |
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WO2017138544A1 true WO2017138544A1 (ja) | 2017-08-17 |
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PCT/JP2017/004489 WO2017138544A1 (ja) | 2016-02-08 | 2017-02-08 | 透明両面粘着シート及び粘着シート積層体 |
Country Status (3)
Country | Link |
---|---|
KR (1) | KR20240017413A (zh) |
TW (1) | TWI799903B (zh) |
WO (1) | WO2017138544A1 (zh) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6360605B1 (ja) * | 2017-08-30 | 2018-07-18 | リンテック株式会社 | 表示体の製造方法 |
JP6438165B1 (ja) * | 2018-06-22 | 2018-12-12 | リンテック株式会社 | 粘着シートおよび表示体 |
WO2019031426A1 (ja) * | 2017-08-08 | 2019-02-14 | 三菱ケミカル株式会社 | 光硬化性粘着シート、光硬化性粘着シート積層体、光硬化性粘着シート積層体の製造方法及び画像表示パネル積層体の製造方法 |
JP2019044024A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 粘着シート、表示体および表示体の製造方法 |
JP2019044023A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 粘着シート、表示体および表示体の製造方法 |
JP2019042965A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 構成体およびその製造方法、表示体、ならびに光学用粘着シート |
WO2020166399A1 (ja) * | 2019-02-12 | 2020-08-20 | 日東電工株式会社 | 補強フィルム |
WO2021131517A1 (ja) * | 2019-12-27 | 2021-07-01 | 日東電工株式会社 | 粘着シート |
WO2021131735A1 (ja) * | 2019-12-27 | 2021-07-01 | 日東電工株式会社 | 粘着シート |
WO2022124000A1 (ja) * | 2020-12-10 | 2022-06-16 | 三菱ケミカル株式会社 | 積層体及び積層構造体 |
US11702571B2 (en) | 2018-03-28 | 2023-07-18 | Lg Chem, Ltd. | Adhesive sheet for temporary fixation and method of manufacturing semiconductor device using the same |
TWI834607B (zh) | 2017-08-30 | 2024-03-11 | 日商琳得科股份有限公司 | 顯示體及顯示體的製造方法 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000104026A (ja) * | 1998-07-27 | 2000-04-11 | Nitto Denko Corp | 紫外線硬化型粘着シ―ト |
JP2006512442A (ja) * | 2002-12-30 | 2006-04-13 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性の感圧接着剤組成物 |
JP2008101104A (ja) * | 2006-10-19 | 2008-05-01 | Denki Kagaku Kogyo Kk | 硬化性組成物 |
JP2013104028A (ja) * | 2011-11-15 | 2013-05-30 | Oji Holdings Corp | 光学部材用両面粘着シートおよび積層体 |
JP2013210598A (ja) * | 2012-03-01 | 2013-10-10 | Mitsubishi Plastics Inc | 偏光板保護用ポリエステルフィルム |
JP2014115468A (ja) * | 2012-12-10 | 2014-06-26 | Nitto Denko Corp | 両面粘着剤付き光学フィルム、およびそれを用いた画像表示装置の製造方法 |
JP2014205735A (ja) * | 2013-04-10 | 2014-10-30 | 王子ホールディングス株式会社 | 多層両面粘着シート、積層体、タッチパネル付表示装置、および多層両面粘着シートの剥離方法 |
WO2015080097A1 (ja) * | 2013-11-29 | 2015-06-04 | 三菱樹脂株式会社 | 粘着剤樹脂組成物 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5138898Y2 (zh) | 1972-10-11 | 1976-09-24 | ||
US8008253B2 (en) | 2007-07-03 | 2011-08-30 | Andrew Tasker | Treatment for anxiety |
JP5195175B2 (ja) | 2008-08-29 | 2013-05-08 | 東京エレクトロン株式会社 | 成膜装置、成膜方法及び記憶媒体 |
-
2017
- 2017-02-08 WO PCT/JP2017/004489 patent/WO2017138544A1/ja active Application Filing
- 2017-02-08 TW TW110123337A patent/TWI799903B/zh active
- 2017-02-08 KR KR1020247002880A patent/KR20240017413A/ko active Application Filing
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000104026A (ja) * | 1998-07-27 | 2000-04-11 | Nitto Denko Corp | 紫外線硬化型粘着シ―ト |
JP2006512442A (ja) * | 2002-12-30 | 2006-04-13 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性の感圧接着剤組成物 |
JP2008101104A (ja) * | 2006-10-19 | 2008-05-01 | Denki Kagaku Kogyo Kk | 硬化性組成物 |
JP2013104028A (ja) * | 2011-11-15 | 2013-05-30 | Oji Holdings Corp | 光学部材用両面粘着シートおよび積層体 |
JP2013210598A (ja) * | 2012-03-01 | 2013-10-10 | Mitsubishi Plastics Inc | 偏光板保護用ポリエステルフィルム |
JP2014115468A (ja) * | 2012-12-10 | 2014-06-26 | Nitto Denko Corp | 両面粘着剤付き光学フィルム、およびそれを用いた画像表示装置の製造方法 |
JP2014205735A (ja) * | 2013-04-10 | 2014-10-30 | 王子ホールディングス株式会社 | 多層両面粘着シート、積層体、タッチパネル付表示装置、および多層両面粘着シートの剥離方法 |
WO2015080097A1 (ja) * | 2013-11-29 | 2015-06-04 | 三菱樹脂株式会社 | 粘着剤樹脂組成物 |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019031426A1 (ja) * | 2017-08-08 | 2019-02-14 | 三菱ケミカル株式会社 | 光硬化性粘着シート、光硬化性粘着シート積層体、光硬化性粘着シート積層体の製造方法及び画像表示パネル積層体の製造方法 |
JP7132702B2 (ja) | 2017-08-30 | 2022-09-07 | リンテック株式会社 | 表示体および表示体の製造方法 |
JP2019044025A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 表示体の製造方法 |
JP2019044024A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 粘着シート、表示体および表示体の製造方法 |
JP2019044023A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 粘着シート、表示体および表示体の製造方法 |
JP2019042965A (ja) * | 2017-08-30 | 2019-03-22 | リンテック株式会社 | 構成体およびその製造方法、表示体、ならびに光学用粘着シート |
JP6360605B1 (ja) * | 2017-08-30 | 2018-07-18 | リンテック株式会社 | 表示体の製造方法 |
TWI834607B (zh) | 2017-08-30 | 2024-03-11 | 日商琳得科股份有限公司 | 顯示體及顯示體的製造方法 |
US11702571B2 (en) | 2018-03-28 | 2023-07-18 | Lg Chem, Ltd. | Adhesive sheet for temporary fixation and method of manufacturing semiconductor device using the same |
JP6438165B1 (ja) * | 2018-06-22 | 2018-12-12 | リンテック株式会社 | 粘着シートおよび表示体 |
JP2019044152A (ja) * | 2018-06-22 | 2019-03-22 | リンテック株式会社 | 粘着シートおよび表示体 |
WO2020166399A1 (ja) * | 2019-02-12 | 2020-08-20 | 日東電工株式会社 | 補強フィルム |
CN114846102A (zh) * | 2019-12-27 | 2022-08-02 | 日东电工株式会社 | 粘合片 |
CN114901770A (zh) * | 2019-12-27 | 2022-08-12 | 日东电工株式会社 | 粘合片 |
WO2021131735A1 (ja) * | 2019-12-27 | 2021-07-01 | 日東電工株式会社 | 粘着シート |
EP4083155A4 (en) * | 2019-12-27 | 2023-11-22 | Nitto Denko Corporation | ADHESIVE SHEET |
WO2021131517A1 (ja) * | 2019-12-27 | 2021-07-01 | 日東電工株式会社 | 粘着シート |
WO2022124000A1 (ja) * | 2020-12-10 | 2022-06-16 | 三菱ケミカル株式会社 | 積層体及び積層構造体 |
Also Published As
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KR20240017413A (ko) | 2024-02-07 |
TWI799903B (zh) | 2023-04-21 |
TW202140723A (zh) | 2021-11-01 |
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