JP2005530025A - 輻射線硬化性、無溶剤型および印刷可能な接着剤前駆物質 - Google Patents
輻射線硬化性、無溶剤型および印刷可能な接着剤前駆物質 Download PDFInfo
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- JP2005530025A JP2005530025A JP2004515718A JP2004515718A JP2005530025A JP 2005530025 A JP2005530025 A JP 2005530025A JP 2004515718 A JP2004515718 A JP 2004515718A JP 2004515718 A JP2004515718 A JP 2004515718A JP 2005530025 A JP2005530025 A JP 2005530025A
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- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 239000003490 Thiodipropionic acid Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229960002130 benzoin Drugs 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
- 230000008033 biological extinction Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 238000010504 bond cleavage reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- KOMDZQSPRDYARS-UHFFFAOYSA-N cyclopenta-1,3-diene titanium Chemical compound [Ti].C1C=CC=C1.C1C=CC=C1 KOMDZQSPRDYARS-UHFFFAOYSA-N 0.000 description 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- UKASIOIEWZDBIT-UHFFFAOYSA-N phenyl-(2,3,4-trimethylphenyl)methanone Chemical compound CC1=C(C)C(C)=CC=C1C(=O)C1=CC=CC=C1 UKASIOIEWZDBIT-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 125000005156 substituted alkylene group Chemical group 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 235000019303 thiodipropionic acid Nutrition 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229960000834 vinyl ether Drugs 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- 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
- C08F290/067—Polyurethanes; Polyureas
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02013605A EP1375618A1 (en) | 2002-06-19 | 2002-06-19 | Radiation-curable, solvent-free and printable precursor of an adhesive |
| PCT/US2003/016607 WO2004000962A1 (en) | 2002-06-19 | 2003-05-28 | Radiation-curable, solvent-free and printable precursor of an adhesive |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005530025A true JP2005530025A (ja) | 2005-10-06 |
| JP2005530025A5 JP2005530025A5 (https=) | 2006-07-13 |
Family
ID=29716794
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004515718A Withdrawn JP2005530025A (ja) | 2002-06-19 | 2003-05-28 | 輻射線硬化性、無溶剤型および印刷可能な接着剤前駆物質 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20050209360A1 (https=) |
| EP (2) | EP1375618A1 (https=) |
| JP (1) | JP2005530025A (https=) |
| CN (1) | CN1285688C (https=) |
| AU (1) | AU2003231859A1 (https=) |
| WO (1) | WO2004000962A1 (https=) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005530024A (ja) * | 2002-06-19 | 2005-10-06 | スリーエム イノベイティブ プロパティズ カンパニー | 放射線硬化性、無溶剤型および印刷可能な感圧接着剤前駆物質 |
| JP2009001765A (ja) * | 2007-05-23 | 2009-01-08 | Hitachi Chem Co Ltd | 接着剤組成物、回路接続構造体及び半導体装置 |
| JP2009527392A (ja) * | 2006-02-23 | 2009-07-30 | スリーエム イノベイティブ プロパティズ カンパニー | 装飾面を有する物品の形成方法 |
| WO2010079584A1 (ja) * | 2009-01-07 | 2010-07-15 | ディーエイチ・マテリアル株式会社 | 粘着剤及び粘着フィルム |
| JP2012136557A (ja) * | 2010-12-24 | 2012-07-19 | Dic Corp | 紫外線硬化型粘着剤用樹脂組成物、粘着剤及び積層体 |
| JP2014005368A (ja) * | 2012-06-25 | 2014-01-16 | Dic Corp | 紫外線硬化型粘着剤用樹脂組成物及び粘着剤 |
| JP2021165329A (ja) * | 2020-04-06 | 2021-10-14 | 東亞合成株式会社 | 活性エネルギー線硬化型接着剤組成物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6949297B2 (en) | 2001-11-02 | 2005-09-27 | 3M Innovative Properties Company | Hybrid adhesives, articles, and methods |
| US6887917B2 (en) * | 2002-12-30 | 2005-05-03 | 3M Innovative Properties Company | Curable pressure sensitive adhesive compositions |
| US7927703B2 (en) | 2003-04-11 | 2011-04-19 | 3M Innovative Properties Company | Adhesive blends, articles, and methods |
| JP2005058288A (ja) * | 2003-08-19 | 2005-03-10 | Three M Innovative Properties Co | 医療用粘着テープのための粘着剤組成物及び粘着テープ |
| US7691437B2 (en) * | 2003-10-31 | 2010-04-06 | 3M Innovative Properties Company | Method for preparing a pressure-sensitive adhesive |
| EP1922378B1 (en) | 2005-09-09 | 2010-05-19 | Avery Dennison Corporation | Heat shrinkable film with (meth)acrylate resin curable adhesive |
| WO2007030584A1 (en) * | 2005-09-09 | 2007-03-15 | Dyna-Tech Adhesives, Incorporated | (meth)acrylate resin curable adhesive |
| US8093322B2 (en) * | 2005-10-27 | 2012-01-10 | Corning Incorporated | Non-reactive additives for fiber coatings |
| US20080121341A1 (en) * | 2006-11-28 | 2008-05-29 | Applied Extrusion Technologies | Radiation curable adhesive with high molecular weight oligomer |
| KR100963497B1 (ko) | 2008-01-31 | 2010-06-17 | 한국다이요잉크 주식회사 | 인쇄회로기판의 잉크젯 마킹용 잉크 조성물과인쇄회로기판의 잉크젯 마킹용 잉크 제조방법 및 마킹방법 |
| US8137957B2 (en) * | 2008-10-22 | 2012-03-20 | Milliken & Company | Non-woven cover for containing and abating odiferous organic emanations |
| EP2382244A1 (en) * | 2008-12-26 | 2011-11-02 | Bomar Specialties Company | Monoisocyanate-acrylate monomers and products utilizing the same |
| KR101740536B1 (ko) * | 2011-01-12 | 2017-05-26 | 동우 화인켐 주식회사 | 광학용 점착제 조성물 |
| DE102011014149B4 (de) * | 2011-03-16 | 2013-04-04 | Wilde Cosmetics Gmbh | Lichthärtender Nagellack |
| KR20120119442A (ko) * | 2011-04-21 | 2012-10-31 | 동우 화인켐 주식회사 | 광학용 감압 점착제 조성물 |
| KR101886432B1 (ko) * | 2011-12-23 | 2018-09-07 | 엘지디스플레이 주식회사 | 유기전계발광표시장치 및 이의 제조 방법 |
| JP5449464B2 (ja) * | 2012-06-27 | 2014-03-19 | シャープ株式会社 | タッチパネルコントローラ、タッチパネル装置および電子情報機器 |
| KR20150095746A (ko) * | 2012-12-10 | 2015-08-21 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 액체 광학 접착제 조성물 |
| GB201310808D0 (en) * | 2013-06-17 | 2013-07-31 | Lumina Adhesives Ab | Medical skin coverings, surgical incision drapes, bacterial barriers for coverin wounds, skin closure devices and methods of treatment using same |
| TWI586780B (zh) | 2015-03-23 | 2017-06-11 | 阿科瑪法國公司 | 壓敏性黏合劑 |
| KR102655948B1 (ko) * | 2015-12-29 | 2024-04-09 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 접착제를 위한 적층 제조 방법 및 접착 물품 |
| KR20190022777A (ko) * | 2016-06-30 | 2019-03-06 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 고점성 성분을 포함하는 인쇄가능 조성물 및 그로부터 3d 물품을 생성하는 방법 |
| US10526511B2 (en) | 2016-12-22 | 2020-01-07 | Avery Dennison Corporation | Convertible pressure sensitive adhesives comprising urethane (meth)acrylate oligomers |
| ES2970716T3 (es) * | 2017-04-04 | 2024-05-30 | Arkema France | Composiciones curables y adhesivos autoadherentes de baja adhesividad preparados a partir de las mismas |
| US11795314B2 (en) | 2017-09-12 | 2023-10-24 | Lg Chem, Ltd. | Encapsulating composition |
| CN109554155B (zh) * | 2017-09-25 | 2021-04-02 | 3M创新有限公司 | 可印刷、可辐射固化的粘合剂组合物及其应用 |
| CN111548739B (zh) * | 2019-02-11 | 2022-03-01 | 3M创新有限公司 | 紫外光固化胶粘剂 |
| CN110283539A (zh) * | 2019-04-25 | 2019-09-27 | 中山布瑞特环保油墨有限公司 | 一种紫外光固化覆膜胶及其制备方法 |
| CN116023596B (zh) * | 2021-10-26 | 2025-09-26 | 明基材料股份有限公司 | 用于牙体修复的成型装置的树脂组合物 |
| WO2025145319A1 (en) * | 2024-01-03 | 2025-07-10 | Henkel Ag & Co. Kgaa | Anti-static photocurable adhesive composition |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53285A (en) * | 1976-06-24 | 1978-01-05 | Gen Electric | Curable composition and coated substances |
| US5475038A (en) * | 1993-08-11 | 1995-12-12 | National Starch And Chemical Investment Holding Corporation | U.V. curable laminating adhesive composition |
| DE19853813A1 (de) * | 1997-12-10 | 1999-06-17 | Henkel Kgaa | Klebstoff mit mehrstufiger Aushärtung und dessen Verwendung bei der Herstellung von Verbundmaterialien |
| WO2004074391A1 (ja) * | 1998-05-08 | 2004-09-02 | Takafumi Iida | 光ディスク貼り合わせ用紫外線硬化型接着剤 |
-
2002
- 2002-06-19 EP EP02013605A patent/EP1375618A1/en not_active Withdrawn
-
2003
- 2003-05-28 AU AU2003231859A patent/AU2003231859A1/en not_active Abandoned
- 2003-05-28 WO PCT/US2003/016607 patent/WO2004000962A1/en not_active Ceased
- 2003-05-28 EP EP03761034A patent/EP1543087A1/en not_active Withdrawn
- 2003-05-28 CN CNB038142562A patent/CN1285688C/zh not_active Expired - Fee Related
- 2003-05-28 US US10/513,123 patent/US20050209360A1/en not_active Abandoned
- 2003-05-28 JP JP2004515718A patent/JP2005530025A/ja not_active Withdrawn
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005530024A (ja) * | 2002-06-19 | 2005-10-06 | スリーエム イノベイティブ プロパティズ カンパニー | 放射線硬化性、無溶剤型および印刷可能な感圧接着剤前駆物質 |
| JP2009527392A (ja) * | 2006-02-23 | 2009-07-30 | スリーエム イノベイティブ プロパティズ カンパニー | 装飾面を有する物品の形成方法 |
| JP2009001765A (ja) * | 2007-05-23 | 2009-01-08 | Hitachi Chem Co Ltd | 接着剤組成物、回路接続構造体及び半導体装置 |
| WO2010079584A1 (ja) * | 2009-01-07 | 2010-07-15 | ディーエイチ・マテリアル株式会社 | 粘着剤及び粘着フィルム |
| JP4794691B2 (ja) * | 2009-01-07 | 2011-10-19 | ディーエイチ・マテリアル株式会社 | 粘着剤及び粘着フィルム |
| JP2012136557A (ja) * | 2010-12-24 | 2012-07-19 | Dic Corp | 紫外線硬化型粘着剤用樹脂組成物、粘着剤及び積層体 |
| JP2014005368A (ja) * | 2012-06-25 | 2014-01-16 | Dic Corp | 紫外線硬化型粘着剤用樹脂組成物及び粘着剤 |
| JP2021165329A (ja) * | 2020-04-06 | 2021-10-14 | 東亞合成株式会社 | 活性エネルギー線硬化型接着剤組成物 |
| JP7452206B2 (ja) | 2020-04-06 | 2024-03-19 | 東亞合成株式会社 | 活性エネルギー線硬化型接着剤組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1375618A1 (en) | 2004-01-02 |
| CN1662621A (zh) | 2005-08-31 |
| CN1285688C (zh) | 2006-11-22 |
| US20050209360A1 (en) | 2005-09-22 |
| EP1543087A1 (en) | 2005-06-22 |
| AU2003231859A1 (en) | 2004-01-06 |
| WO2004000962A1 (en) | 2003-12-31 |
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