JPH07505431A - 紫外線硬化性アクリレート感圧接着剤組成物 - Google Patents
紫外線硬化性アクリレート感圧接着剤組成物Info
- Publication number
- JPH07505431A JPH07505431A JP5517493A JP51749393A JPH07505431A JP H07505431 A JPH07505431 A JP H07505431A JP 5517493 A JP5517493 A JP 5517493A JP 51749393 A JP51749393 A JP 51749393A JP H07505431 A JPH07505431 A JP H07505431A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- free radical
- polymer
- composition
- 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.)
- Pending
Links
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- 125000003118 aryl group Chemical group 0.000 description 1
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- MRVHGCMXWNDJBQ-UHFFFAOYSA-N benzyl carbamodithioate Chemical compound NC(=S)SCC1=CC=CC=C1 MRVHGCMXWNDJBQ-UHFFFAOYSA-N 0.000 description 1
- HLZBIKHKXIJIHX-UHFFFAOYSA-N benzyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SCC1=CC=CC=C1 HLZBIKHKXIJIHX-UHFFFAOYSA-N 0.000 description 1
- ISIHGMPTSUWCKF-UHFFFAOYSA-N benzyl n-ethylcarbamodithioate Chemical compound CCNC(=S)SCC1=CC=CC=C1 ISIHGMPTSUWCKF-UHFFFAOYSA-N 0.000 description 1
- BVBCEEGYULUZFK-UHFFFAOYSA-N benzyl n-methylcarbamodithioate Chemical compound CNC(=S)SCC1=CC=CC=C1 BVBCEEGYULUZFK-UHFFFAOYSA-N 0.000 description 1
- RBGLVWCAGPITBS-UHFFFAOYSA-L bis(trifluoromethylsulfonyloxy)tin Chemical compound [Sn+2].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F RBGLVWCAGPITBS-UHFFFAOYSA-L 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NRJXPXBNIOUCGG-UHFFFAOYSA-N butyl n,n-dimethylcarbamodithioate Chemical compound CCCCSC(=S)N(C)C NRJXPXBNIOUCGG-UHFFFAOYSA-N 0.000 description 1
- RFJZMPMMBCKYGX-UHFFFAOYSA-N butyl prop-2-enoate;methyl prop-2-enoate Chemical compound COC(=O)C=C.CCCCOC(=O)C=C RFJZMPMMBCKYGX-UHFFFAOYSA-N 0.000 description 1
- CSNJTIWCTNEOSW-UHFFFAOYSA-N carbamothioylsulfanyl carbamodithioate Chemical compound NC(=S)SSC(N)=S CSNJTIWCTNEOSW-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000013078 crystal 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
- 235000013367 dietary fats Nutrition 0.000 description 1
- 125000005805 dimethoxy phenyl group Chemical group 0.000 description 1
- MZGNSEAPZQGJRB-UHFFFAOYSA-N dimethyldithiocarbamic acid Chemical compound CN(C)C(S)=S MZGNSEAPZQGJRB-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- DAPKEMXFFNUVPN-UHFFFAOYSA-N ethylcarbamothioyl n-ethylcarbamodithioate Chemical compound CCNC(=S)SC(=S)NCC DAPKEMXFFNUVPN-UHFFFAOYSA-N 0.000 description 1
- KUDUQBURMYMBIJ-UHFFFAOYSA-N ethylene glycol diacrylate Substances C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000010520 ghee Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000008863 intramolecular interaction Effects 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
- 238000003475 lamination Methods 0.000 description 1
- 230000014759 maintenance of location Effects 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
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- URLKBWYHVLBVBO-UHFFFAOYSA-N p-dimethylbenzene Natural products CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- GKROKAVBUIADBS-UHFFFAOYSA-N phenanthrene-2-carbaldehyde Chemical compound C1=CC=C2C3=CC=C(C=O)C=C3C=CC2=C1 GKROKAVBUIADBS-UHFFFAOYSA-N 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920006264 polyurethane film Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 229920005609 vinylidenefluoride/hexafluoropropylene copolymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block 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
- 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
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)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86124292A | 1992-03-31 | 1992-03-31 | |
| US861,242 | 1992-03-31 | ||
| PCT/US1993/002528 WO1993020164A1 (fr) | 1992-03-31 | 1993-03-19 | Compositions auto-adhesives d'acrylate durcissables par rayonnement ultraviolet |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07505431A true JPH07505431A (ja) | 1995-06-15 |
Family
ID=25335262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5517493A Pending JPH07505431A (ja) | 1992-03-31 | 1993-03-19 | 紫外線硬化性アクリレート感圧接着剤組成物 |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0633918A1 (fr) |
| JP (1) | JPH07505431A (fr) |
| KR (1) | KR950700973A (fr) |
| WO (1) | WO1993020164A1 (fr) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001348553A (ja) * | 2000-06-06 | 2001-12-18 | Nitto Denko Corp | 粘着剤組成物とその粘着シ―ト類およびこれらの製造方法 |
| JP2002167566A (ja) * | 2000-12-01 | 2002-06-11 | Nitto Denko Corp | 紫外線架橋型粘着剤組成物とその製造方法ならびに粘着シ―トとその製造方法 |
| JP2009167421A (ja) * | 1997-12-18 | 2009-07-30 | Commonwealth Scientific & Industrial Research Organisation | リビング性を有する重合方法およびその方法で製造されるポリマー |
| JP2013507759A (ja) * | 2009-10-08 | 2013-03-04 | アルケマ フランス | 太陽電池モジュール |
| JP2013527874A (ja) * | 2010-05-03 | 2013-07-04 | アルケマ フランス | Ｕｖ硬化性封止剤 |
| JP2017509714A (ja) * | 2014-02-20 | 2017-04-06 | エルジー・ケム・リミテッド | ゴム系粘着剤組成物およびそれを用いた自動車用ゴム系粘着テープ |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5773485A (en) * | 1994-07-29 | 1998-06-30 | Minnesota Mining And Manufacturing Company | Acrylic syrup curable to a crosslinked viscoelastomeric material |
| FR2771747B1 (fr) * | 1997-12-03 | 2003-09-26 | Atochem Elf Sa | Utilisation de copolymeres a blocs lineaires non-dieniques comme auto-adhesifs ou composants d'auto-adhesifs |
| DE10248380A1 (de) * | 2002-10-17 | 2004-08-05 | Tesa Ag | Haftklebrige Formteile |
| FR2884254B1 (fr) * | 2005-04-08 | 2007-05-25 | Arkema Sa | Copolymere sequence a fonctions acides modulables et composition adhesive et thermoplastique le contenant |
| JP5654876B2 (ja) * | 2009-01-22 | 2015-01-14 | 日本製紙株式会社 | 活性エネルギー線硬化型樹脂組成物 |
| WO2011048802A1 (fr) * | 2009-10-23 | 2011-04-28 | クラレメディカル株式会社 | Composition polymérisable et matériau dentaire |
| JP6949099B2 (ja) * | 2016-07-11 | 2021-10-13 | スリーエム イノベイティブ プロパティズ カンパニー | ポリマー材料及び制御ラジカル開始剤を使用した製造方法 |
| CN110099938B (zh) * | 2016-12-22 | 2021-01-15 | 3M创新有限公司 | 可交联聚合物材料和交联聚合物材料 |
| WO2019123182A1 (fr) * | 2017-12-21 | 2019-06-27 | 3M Innovative Properties Company | Compositions polymères préparées avec un initiateur radicalaire contrôlé |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2553134B2 (ja) * | 1987-04-07 | 1996-11-13 | 三菱化学株式会社 | Ａｂａ型ブロック共重合体 |
| AU614140B2 (en) * | 1988-06-28 | 1991-08-22 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive |
| DE69006472T2 (de) * | 1989-12-21 | 1994-09-01 | Minnesota Mining & Mfg | Zahnärztliche Zusammensetzungen, Verfahren zur Herstellung von geformten, zahnärztlichen Artikeln via "photoiniferte Polymerisation" von zahnärztlichen Zusammensetzungen und dadurch erzeugte geformte, zahnärztliche Artikel. |
| CA2038117A1 (fr) * | 1990-03-29 | 1991-09-30 | Mahfuza B. Ali | Composes adhesifs a photodurcissement controle pour fixer les dispositifs microelectroniques et methode de fixation de dispositifs microelectroniques avec ces composes |
-
1993
- 1993-03-19 EP EP93907594A patent/EP0633918A1/fr not_active Ceased
- 1993-03-19 JP JP5517493A patent/JPH07505431A/ja active Pending
- 1993-03-19 WO PCT/US1993/002528 patent/WO1993020164A1/fr not_active Ceased
-
1994
- 1994-09-29 KR KR1019940703387A patent/KR950700973A/ko not_active Withdrawn
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009167421A (ja) * | 1997-12-18 | 2009-07-30 | Commonwealth Scientific & Industrial Research Organisation | リビング性を有する重合方法およびその方法で製造されるポリマー |
| JP2001348553A (ja) * | 2000-06-06 | 2001-12-18 | Nitto Denko Corp | 粘着剤組成物とその粘着シ―ト類およびこれらの製造方法 |
| JP2002167566A (ja) * | 2000-12-01 | 2002-06-11 | Nitto Denko Corp | 紫外線架橋型粘着剤組成物とその製造方法ならびに粘着シ―トとその製造方法 |
| JP2013507759A (ja) * | 2009-10-08 | 2013-03-04 | アルケマ フランス | 太陽電池モジュール |
| JP2013527874A (ja) * | 2010-05-03 | 2013-07-04 | アルケマ フランス | Ｕｖ硬化性封止剤 |
| JP2017509714A (ja) * | 2014-02-20 | 2017-04-06 | エルジー・ケム・リミテッド | ゴム系粘着剤組成物およびそれを用いた自動車用ゴム系粘着テープ |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1993020164A1 (fr) | 1993-10-14 |
| EP0633918A1 (fr) | 1995-01-18 |
| KR950700973A (ko) | 1995-02-20 |
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