NO311137B1 - Fremgangsmåte for herding av en UV-herdbar blokk- kopolymerblanding ved eksponering av blandingen for UV-stråling ien oksygenholdig atmosf¶re - Google Patents
Fremgangsmåte for herding av en UV-herdbar blokk- kopolymerblanding ved eksponering av blandingen for UV-stråling ien oksygenholdig atmosf¶re Download PDFInfo
- Publication number
- NO311137B1 NO311137B1 NO19960130A NO960130A NO311137B1 NO 311137 B1 NO311137 B1 NO 311137B1 NO 19960130 A NO19960130 A NO 19960130A NO 960130 A NO960130 A NO 960130A NO 311137 B1 NO311137 B1 NO 311137B1
- Authority
- NO
- Norway
- Prior art keywords
- block copolymer
- weight
- mixture
- photoinitiator
- parts
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 229920001400 block copolymer Polymers 0.000 title claims abstract description 37
- 230000005855 radiation Effects 0.000 title claims description 20
- 238000000034 method Methods 0.000 title claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims description 11
- 239000001301 oxygen Substances 0.000 title claims description 11
- 229910052760 oxygen Inorganic materials 0.000 title claims description 11
- 239000012298 atmosphere Substances 0.000 title claims description 9
- 229920000642 polymer Polymers 0.000 claims abstract description 17
- 150000001491 aromatic compounds Chemical class 0.000 claims abstract description 9
- 150000001993 dienes Chemical class 0.000 claims abstract description 8
- 125000003118 aryl group Chemical group 0.000 claims abstract description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 7
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 17
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 10
- 239000012965 benzophenone Substances 0.000 claims description 10
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 claims description 9
- 239000003431 cross linking reagent Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 150000003512 tertiary amines Chemical class 0.000 claims description 6
- WXPWZZHELZEVPO-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 WXPWZZHELZEVPO-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000007822 coupling agent Substances 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- HPAFOABSQZMTHE-UHFFFAOYSA-N phenyl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)C1=CC=CC=C1 HPAFOABSQZMTHE-UHFFFAOYSA-N 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 150000001728 carbonyl compounds Chemical class 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 238000009472 formulation Methods 0.000 description 20
- 238000001723 curing Methods 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 230000001070 adhesive effect Effects 0.000 description 11
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 9
- 229920001971 elastomer Polymers 0.000 description 8
- 230000004927 fusion Effects 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 6
- 229920002633 Kraton (polymer) Polymers 0.000 description 6
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000004831 Hot glue Substances 0.000 description 5
- -1 polybutylene Polymers 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 229920006295 polythiol Polymers 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000000565 sealant Substances 0.000 description 4
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000003848 UV Light-Curing Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012943 hotmelt Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- 241000765083 Ondina Species 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 239000010690 paraffinic oil Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000003504 photosensitizing agent Substances 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- AHAREKHAZNPPMI-AATRIKPKSA-N (3e)-hexa-1,3-diene Chemical compound CC\C=C\C=C AHAREKHAZNPPMI-AATRIKPKSA-N 0.000 description 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- HBKBEZURJSNABK-MWJPAGEPSA-N 2,3-dihydroxypropyl (1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(=O)OCC(O)CO HBKBEZURJSNABK-MWJPAGEPSA-N 0.000 description 1
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- IKVYHNPVKUNCJM-UHFFFAOYSA-N 4-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(C(C)C)=CC=C2 IKVYHNPVKUNCJM-UHFFFAOYSA-N 0.000 description 1
- APMOEFCWQRJOPS-UHFFFAOYSA-N 5-ethenyl-1,5-dimethylcyclohexa-1,3-diene Chemical compound CC1=CC=CC(C)(C=C)C1 APMOEFCWQRJOPS-UHFFFAOYSA-N 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000374 eutectic mixture Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229920000428 triblock copolymer Polymers 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
-
- 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
- C08K5/07—Aldehydes; Ketones
-
- 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
- C08K5/17—Amines; Quaternary ammonium compounds
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/378—Thiols containing heterocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polymerisation Methods In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP93202072 | 1993-07-14 | ||
| EP94200599 | 1994-03-08 | ||
| PCT/EP1994/002314 WO1995002640A1 (en) | 1993-07-14 | 1994-07-12 | Uv-curable block copolymer composition |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO960130D0 NO960130D0 (no) | 1996-01-11 |
| NO960130L NO960130L (no) | 1996-03-12 |
| NO311137B1 true NO311137B1 (no) | 2001-10-15 |
Family
ID=26133915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19960130A NO311137B1 (no) | 1993-07-14 | 1996-01-11 | Fremgangsmåte for herding av en UV-herdbar blokk- kopolymerblanding ved eksponering av blandingen for UV-stråling ien oksygenholdig atmosf¶re |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JP3420240B2 (sv) |
| CN (1) | CN1067416C (sv) |
| AT (1) | ATE171972T1 (sv) |
| AU (1) | AU688361B2 (sv) |
| BR (1) | BR9407055A (sv) |
| CA (1) | CA2167185A1 (sv) |
| DE (1) | DE69413823T2 (sv) |
| DK (1) | DK0708802T3 (sv) |
| ES (1) | ES2122320T3 (sv) |
| FI (1) | FI960137A (sv) |
| MX (1) | MX9405293A (sv) |
| NO (1) | NO311137B1 (sv) |
| WO (1) | WO1995002640A1 (sv) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2324303A (en) * | 1997-04-03 | 1998-10-21 | Shell Int Research | Bituminous composition |
| US6326127B1 (en) * | 1998-12-31 | 2001-12-04 | Kraton Polymers U.S. Llc | Photo-curable polymer composition and flexographic printing plates containing the same |
| DE10049669A1 (de) | 2000-10-06 | 2002-04-11 | Tesa Ag | Verfahren zur Herstellung von vernetzten Acrylatschmelzhaftklebemassen |
| CN1934188B (zh) * | 2004-03-25 | 2010-05-05 | 克雷顿聚合物研究公司 | 可通过暴露于辐射而转变成热固性凝胶组合物的热塑性凝胶组合物 |
| US7560503B2 (en) * | 2004-06-03 | 2009-07-14 | Kraton Polymers U.S. Llc | Gels from high molecular weight block copolymers |
| KR100834514B1 (ko) * | 2005-10-17 | 2008-06-02 | 재단법인서울대학교산학협력재단 | 핫멜트형 점착제 성분이 포함된 자외선 경화형 핫멜트점착제조성물 및 점착테이프 |
| CN101547989B (zh) | 2006-12-07 | 2011-07-06 | 3M创新有限公司 | 嵌段共聚物和丙烯酸类粘合剂的共混物 |
| JP2013539072A (ja) * | 2010-09-16 | 2013-10-17 | エルジー・ケム・リミテッド | 感光性樹脂組成物、ドライフィルムソルダーレジスト及び回路基板 |
| EP3357968A4 (en) | 2015-09-30 | 2019-06-12 | Zeon Corporation | BLOCK COPOLYMER COMPOSITION AND THERMOFUSIBLE ADHESIVE COMPOSITION |
| CN107674596B (zh) * | 2016-08-02 | 2020-10-13 | 滕超 | 一种基于可紫外光固化苯乙烯嵌段共聚物胶粘剂的可拉伸剥离胶粘带及其制备方法 |
| CN117417726B (zh) * | 2023-12-15 | 2024-03-15 | 广州鹿山新材料股份有限公司 | Uv固化橡胶系压敏胶及其制备方法和应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4556464A (en) * | 1983-04-04 | 1985-12-03 | Shell Oil Company | Endblock crosslinked block copolymer adhesive composition |
| US5270388A (en) * | 1990-04-27 | 1993-12-14 | Nippon Zeon Co., Ltd. | Shape-memorizing block copolymer composition |
| TW274086B (sv) * | 1992-06-04 | 1996-04-11 | Shell Internat Res Schappej Bv |
-
1994
- 1994-07-12 MX MX9405293A patent/MX9405293A/es not_active IP Right Cessation
- 1994-07-12 JP JP50434695A patent/JP3420240B2/ja not_active Expired - Lifetime
- 1994-07-12 BR BR9407055A patent/BR9407055A/pt not_active IP Right Cessation
- 1994-07-12 CN CN94192754A patent/CN1067416C/zh not_active Expired - Lifetime
- 1994-07-12 ES ES94924758T patent/ES2122320T3/es not_active Expired - Lifetime
- 1994-07-12 AU AU74932/94A patent/AU688361B2/en not_active Ceased
- 1994-07-12 DK DK94924758T patent/DK0708802T3/da active
- 1994-07-12 WO PCT/EP1994/002314 patent/WO1995002640A1/en active IP Right Grant
- 1994-07-12 AT AT94924758T patent/ATE171972T1/de not_active IP Right Cessation
- 1994-07-12 CA CA002167185A patent/CA2167185A1/en not_active Abandoned
- 1994-07-12 DE DE69413823T patent/DE69413823T2/de not_active Expired - Lifetime
-
1996
- 1996-01-11 FI FI960137A patent/FI960137A/sv unknown
- 1996-01-11 NO NO19960130A patent/NO311137B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69413823T2 (de) | 1999-03-18 |
| NO960130D0 (no) | 1996-01-11 |
| DK0708802T3 (da) | 1999-06-21 |
| DE69413823D1 (de) | 1998-11-12 |
| WO1995002640A1 (en) | 1995-01-26 |
| AU7493294A (en) | 1995-02-13 |
| CN1067416C (zh) | 2001-06-20 |
| AU688361B2 (en) | 1998-03-12 |
| CN1127008A (zh) | 1996-07-17 |
| NO960130L (no) | 1996-03-12 |
| ES2122320T3 (es) | 1998-12-16 |
| JPH09500156A (ja) | 1997-01-07 |
| BR9407055A (pt) | 1996-08-13 |
| FI960137A0 (sv) | 1996-01-11 |
| MX9405293A (es) | 1995-01-31 |
| JP3420240B2 (ja) | 2003-06-23 |
| ATE171972T1 (de) | 1998-10-15 |
| CA2167185A1 (en) | 1995-01-26 |
| FI960137A (sv) | 1996-01-11 |
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