JP6859344B2 - 感圧接着剤のための熱可逆性ポリマーの架橋 - Google Patents
感圧接着剤のための熱可逆性ポリマーの架橋 Download PDFInfo
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- JP6859344B2 JP6859344B2 JP2018526258A JP2018526258A JP6859344B2 JP 6859344 B2 JP6859344 B2 JP 6859344B2 JP 2018526258 A JP2018526258 A JP 2018526258A JP 2018526258 A JP2018526258 A JP 2018526258A JP 6859344 B2 JP6859344 B2 JP 6859344B2
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- adhesive composition
- acrylate
- thermoreversible
- furfuryl
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 title claims description 18
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- 238000004132 cross linking Methods 0.000 title description 2
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- 230000001070 adhesive effect Effects 0.000 claims description 51
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- 239000000178 monomer Substances 0.000 claims description 23
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 claims description 21
- 229920003192 poly(bis maleimide) Polymers 0.000 claims description 21
- 229920001577 copolymer Polymers 0.000 claims description 18
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 12
- 230000004913 activation Effects 0.000 claims description 11
- 238000000576 coating method Methods 0.000 claims description 9
- 239000003431 cross linking reagent Substances 0.000 claims description 9
- DWXAVNJYFLGAEF-UHFFFAOYSA-N furan-2-ylmethyl 2-methylprop-2-enoate Chemical group CC(=C)C(=O)OCC1=CC=CO1 DWXAVNJYFLGAEF-UHFFFAOYSA-N 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 8
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- 238000012360 testing method Methods 0.000 description 8
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
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- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
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- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
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- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
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- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004626 polylactic acid Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
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- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
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- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-UHFFFAOYSA-N 0.000 description 1
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- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
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- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- 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 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 238000006845 Michael addition reaction Methods 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical class OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 1
- 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 1
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- 238000013019 agitation Methods 0.000 description 1
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
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- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
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- MBAQOFIMVJQPOE-UHFFFAOYSA-N butane;pyrrole-2,5-dione Chemical compound CCCC.O=C1NC(=O)C=C1 MBAQOFIMVJQPOE-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
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- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
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- 239000000839 emulsion Substances 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
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- 229910052742 iron Inorganic materials 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
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- 239000010893 paper waste Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
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- 229920000098 polyolefin Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
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- 239000006254 rheological additive Substances 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
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- 239000007858 starting material Substances 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
-
- 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
- C08F220/12—Esters of monohydric alcohols or 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
- 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
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- 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
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- 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
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1808—C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
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- 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
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
-
- 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
- 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
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
-
- 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
- C08F2810/00—Chemical modification of a polymer
- C08F2810/20—Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
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- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/334—Applications of adhesives in processes or use of adhesives in the form of films or foils as a label
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/50—Additional features of adhesives in the form of films or foils characterized by process specific features
- C09J2301/502—Additional features of adhesives in the form of films or foils characterized by process specific features process for debonding adherents
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- C—CHEMISTRY; METALLURGY
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- C09J2433/00—Presence of (meth)acrylic polymer
Description
本出願は、2015年11月23日に出願された米国仮特許出願第62/258,936号の利益を主張する。
本出願が提供する発明として、例えば以下のものが挙げられる。
[1] 熱可逆性接着剤組成物であって、
a)
i)共役ジエンアクリレートまたはメタクリレートと
ii)少なくとも1つのアクリルモノマーと、
のコポリマーと、
b)ビスマレイミド架橋剤と、
を含む、熱可逆性接着剤組成物。
[2] 粘着付与剤をさらに含む、[1]に記載の熱可逆性接着剤組成物。
[3] 前記共役ジエンアクリレートまたはメタクリレートは、フルフリルメタクリレートである、[1]に記載の熱可逆性接着剤組成物。
[4] 前記フルフリルメタクリレート官能基は、0.5重量パーセント〜10重量パーセントの範囲で前記コポリマー中に存在する、[1]に記載の熱可逆性接着剤組成物。
[5] 前記ビスマレイミド架橋剤は、ビス(3−エチル−5−メチル−4−マレイミドフェニル)メタンである、[1]に記載の熱可逆性接着剤組成物。
[6] [1]に記載の熱可逆性接着剤組成物を調製するためのプロセスであって、
a)
i)共役ジエンアクリレートまたはメタクリレートと
ii)少なくとも1つのアクリルモノマーと、
のコポリマーと、
b)ビスマレイミド架橋剤と、
を混合することを含む、プロセス。
[7] 前記共役ジエンアクリレートは、フルフリルメタクリレートである、[6]に記載のプロセス。
[8] [1]に記載の熱可逆性接着剤組成物から調製される、熱活性化感圧接着剤組成物。
[9] [1]に記載の熱可逆性接着剤組成物から調製される、ヒートシールコーティング。
[10] [1]に記載の熱可逆性接着剤組成物から調製される、インモールドラベル。
[11] [1]に記載の熱可逆性接着剤組成物から調製される、ライナーレスラベル。
フルフリルメタクリレートを用いたまたは用いないアクリルモノマーのフリーラジカル重合によって、酢酸エチル中にコポリマーを合成した。80gの酢酸エチルを含む冷却管を備えたフラスコを、窒素ブランケット下で77℃まで加熱した。開始剤として2.85gのVAZO 64(AIBN)、及び27gの酢酸エチルを含有する溶液を0.1mL/分で供給し、5分後に、390gの酢酸エチル及び300gのモノマーを含有するモノマー溶液を3.64g/分で供給した。これらの供給を190分間継続した。モノマーの供給が終了した後、開始剤の供給を同じ速度で30分間続けた。あらゆる未反応モノマーを変換させるために、開始剤の供給量を30分間0.35mL/分まで増加させた。反応終了時に、さらに精製することなく混合物を冷却した。フルフリルメタクリレートポリマーは、重合中に淡黄色に変化した。
1.6ミル間隙のバードバーを用いて、Cheminstrumentsの2ミルPET未処理フィルム上にコーティングを作製し、次いで、空気乾燥させて約0.8ミルのコーティングを作製した。接着剤でコーティングされたフィルムをステンレス鋼パネル上で試験した。PSTC 101 Testの方法A、180度剥離試験を用いて、接着剤でコーティングされたフィルムを除去する力を試料1インチ当たりのニュートンとしてインストロンで測定した。滞留時間は、ステンレス鋼試験パネルに対する接着剤の貼付と、接着剤をコーティングされたフィルムが試験のために除去された時との間の時間を反映している。観察された破壊モード(FM)は、接着剤自体が内側から破壊する凝集破壊(C)、または接着剤が基板からきれいに除去される接着破壊(A)のいずれかであった。活性化は、下の表4及び表5に示される温度及び活性化時間で、Mathisオーブン内で行われた。
Claims (9)
- 熱可逆性接着剤組成物であって、
a)
i)フルフリル(メタ)アクリレートと
ii)少なくとも1つのアクリルモノマーと、
のコポリマーと、
b)ビス(3−エチル−5−メチル−4−マレイミドフェニル)メタンである、ビスマレイミド架橋剤と、
を含み、110℃〜200℃の活性化温度を有する、熱可逆性接着剤組成物。 - 粘着付与剤をさらに含む、請求項1に記載の熱可逆性接着剤組成物。
- 前記フルフリル(メタ)アクリレートは、フルフリルメタクリレートである、請求項1に記載の熱可逆性接着剤組成物。
- 請求項1に記載の熱可逆性接着剤組成物を調製するためのプロセスであって、
a)
i)フルフリル(メタ)アクリレートと
ii)少なくとも1つのアクリルモノマーと、
のコポリマーと、
b)ビス(3−エチル−5−メチル−4−マレイミドフェニル)メタンである、ビスマレイミド架橋剤と、
を混合することを含む、プロセス。 - 前記フルフリル(メタ)アクリレートは、フルフリルメタクリレートである、請求項4に記載のプロセス。
- 請求項1に記載の熱可逆性接着剤組成物から調製される、熱活性化感圧接着剤組成物。
- 請求項1に記載の熱可逆性接着剤組成物から調製される、ヒートシールコーティング。
- 請求項1に記載の熱可逆性接着剤組成物から調製される、インモールドラベル。
- 請求項1に記載の熱可逆性接着剤組成物から調製される、ライナーレスラベル。
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US201562258936P | 2015-11-23 | 2015-11-23 | |
US62/258,936 | 2015-11-23 | ||
PCT/US2016/052735 WO2017091284A1 (en) | 2015-11-23 | 2016-09-21 | Thermally reversible polymer crosslinking for pressure sensitive adhesives |
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JP6859344B2 true JP6859344B2 (ja) | 2021-04-14 |
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US (1) | US10731053B2 (ja) |
EP (1) | EP3380535B1 (ja) |
JP (1) | JP6859344B2 (ja) |
CN (1) | CN108350126B (ja) |
AR (1) | AR106710A1 (ja) |
BR (1) | BR112018010069B1 (ja) |
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DE102018211720A1 (de) | 2018-07-13 | 2020-01-16 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Funktionalisierte Polymere |
US11440868B2 (en) * | 2019-07-22 | 2022-09-13 | Board Of Trustees Of Michigan State University | Reversible adhesive compositions, related articles, and related methods |
US11634616B1 (en) | 2022-06-30 | 2023-04-25 | CreateMe Technologies LLC | Methods of assembling apparel products having boronate adhesives |
US11655397B1 (en) | 2022-06-30 | 2023-05-23 | CreateMe Technologies LLC | Methods of assembling apparel products having cycloalkene adhesives |
US11530336B1 (en) | 2022-06-30 | 2022-12-20 | CreateMe Technologies LLC | Methods of assembling apparel products having cyclodextrin-azobenzene adhesives |
US11752234B1 (en) | 2022-06-30 | 2023-09-12 | CreateMe Technologies LLC | Shape memory adhesives for apparel products |
US11692111B1 (en) | 2022-06-30 | 2023-07-04 | CreateMe Technologies LLC | Methods of disassembling apparel products having shape memory adhesives |
US11857013B1 (en) | 2022-06-30 | 2024-01-02 | Createme Technologies Inc. | Methods of assembling apparel products having shape memory adhesives |
US11530340B1 (en) | 2022-06-30 | 2022-12-20 | CreateMe Technologies LLC | Cyclodextrin-azobenzene adhesives for apparel products |
US11629272B1 (en) | 2022-06-30 | 2023-04-18 | CreateMe Technologies LLC | Methods of assembling apparel products having thioester adhesives |
US11732159B1 (en) | 2022-06-30 | 2023-08-22 | CreateMe Technologies LLC | Methods of disassembling apparel products having boronate adhesives |
US11632995B1 (en) | 2022-06-30 | 2023-04-25 | CreateMe Technologies LLC | Methods of assembling apparel products having disulfide adhesives |
US11712873B1 (en) | 2022-06-30 | 2023-08-01 | CreateMe Technologies LLC | Boronate adhesives for apparel products |
US11653709B1 (en) | 2022-06-30 | 2023-05-23 | CreateMe Technologies LLC | Methods of disassembling apparel products having disulfide adhesives |
US11542412B1 (en) | 2022-06-30 | 2023-01-03 | CreateMe Technologies LLC | Methods of disassembling apparel products having cyclodextrin-azobenzene adhesives |
US11849791B1 (en) | 2022-06-30 | 2023-12-26 | Createme Technologies Inc. | Methods of assembling apparel products having imine adhesives |
US11713405B1 (en) | 2022-06-30 | 2023-08-01 | CreateMe Technologies LLC | Methods of disassembling apparel products having thioester adhesives |
US11730215B1 (en) | 2022-06-30 | 2023-08-22 | CreateMe Technologies LLC | Thioester adhesives for apparel products |
US11730217B1 (en) | 2022-06-30 | 2023-08-22 | CreateMe Technologies LLC | Methods of disassembling apparel products having cycloalkene adhesives |
US11905440B1 (en) | 2022-06-30 | 2024-02-20 | Createme Technologies Inc. | Disulfide adhesives for apparel products |
US11542413B1 (en) | 2022-06-30 | 2023-01-03 | CreateMe Technologies LLC | Methods of disassembling apparel products having imine adhesives |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4104319A1 (de) * | 1991-02-13 | 1992-08-20 | Roehm Gmbh | Reversibel vernetzte, thermoplastisch verarbeitbare polymethacrylat-formmasse |
DE19909212A1 (de) * | 1999-03-03 | 2000-09-07 | Basf Ag | Durch Diels-Alder-Reaktion vernetzbare Polymere |
US7288161B2 (en) | 2004-07-15 | 2007-10-30 | International Business Machines Corporation | Reworkable adhesives containing thermally labile groups |
WO2007083810A1 (ja) * | 2006-01-23 | 2007-07-26 | Hitachi Chemical Co., Ltd. | 接着剤組成物、フィルム状接着剤、接着シート、並びにそれを用いた半導体装置 |
CN102186938B (zh) * | 2008-01-28 | 2013-11-06 | Upm拉弗拉塔克公司 | 标签和用于将该标签贴附到物体上的方法 |
WO2010144774A2 (en) | 2009-06-11 | 2010-12-16 | Henkel Corporation | Thermally reversible hot melt adhesive composition containing multifunctional diene and dienophile compounds |
EP2434528A1 (en) * | 2010-09-28 | 2012-03-28 | Nederlandse Organisatie voor toegepast -natuurwetenschappelijk onderzoek TNO | An active carrier for carrying a wafer and method for release |
US8917510B2 (en) | 2011-01-14 | 2014-12-23 | International Business Machines Corporation | Reversibly adhesive thermal interface material |
JP2013035933A (ja) * | 2011-08-05 | 2013-02-21 | Nitto Denko Corp | 粘着シート |
DE102012222742A1 (de) | 2012-12-11 | 2014-03-27 | Evonik Industries Ag | Funktionsmaterialien mit reversibler Vernetzung |
JP6460367B2 (ja) * | 2014-03-26 | 2019-01-30 | ニッタ株式会社 | 仮固定用両面粘着テープおよびそれを用いた被加工物の仮固定方法 |
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