WO1996029373A1 - Composition d'adhesif autocollant dispersable dans l'eau, son procede de production, et articles adhesifs autocollants fabriques a partir de cette composition - Google Patents
Composition d'adhesif autocollant dispersable dans l'eau, son procede de production, et articles adhesifs autocollants fabriques a partir de cette composition Download PDFInfo
- Publication number
- WO1996029373A1 WO1996029373A1 PCT/JP1996/000740 JP9600740W WO9629373A1 WO 1996029373 A1 WO1996029373 A1 WO 1996029373A1 JP 9600740 W JP9600740 W JP 9600740W WO 9629373 A1 WO9629373 A1 WO 9629373A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- sensitive adhesive
- pressure
- water
- compound
- Prior art date
Links
- 239000004820 Pressure-sensitive adhesive Substances 0.000 title claims abstract description 187
- 239000000203 mixture Substances 0.000 title claims abstract description 76
- 238000004519 manufacturing process Methods 0.000 title claims description 38
- 238000000034 method Methods 0.000 title description 28
- 150000001875 compounds Chemical class 0.000 claims abstract description 128
- 239000002270 dispersing agent Substances 0.000 claims abstract description 101
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 94
- 125000000524 functional group Chemical group 0.000 claims abstract description 77
- 229910052751 metal Inorganic materials 0.000 claims abstract description 25
- 239000002184 metal Substances 0.000 claims abstract description 25
- 229920000642 polymer Polymers 0.000 claims description 98
- 239000000178 monomer Substances 0.000 claims description 60
- -1 acrylate ester Chemical class 0.000 claims description 38
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 33
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 25
- 125000003277 amino group Chemical group 0.000 claims description 23
- 239000010410 layer Substances 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 claims description 17
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 16
- 125000003172 aldehyde group Chemical group 0.000 claims description 15
- 125000004069 aziridinyl group Chemical group 0.000 claims description 15
- 125000005968 oxazolinyl group Chemical group 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 5
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 abstract description 3
- 230000001070 adhesive effect Effects 0.000 description 40
- 239000000853 adhesive Substances 0.000 description 35
- 239000006185 dispersion Substances 0.000 description 34
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 18
- 238000006116 polymerization reaction Methods 0.000 description 17
- 239000003995 emulsifying agent Substances 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- 238000007720 emulsion polymerization reaction Methods 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 12
- 238000007654 immersion Methods 0.000 description 12
- 239000002390 adhesive tape Substances 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000010556 emulsion polymerization method Methods 0.000 description 6
- 150000002736 metal compounds Chemical class 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000002194 synthesizing effect Effects 0.000 description 6
- 230000002087 whitening effect Effects 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- PMBXCGGQNSVESQ-UHFFFAOYSA-N 1-Hexanethiol Chemical compound CCCCCCS PMBXCGGQNSVESQ-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 239000013522 chelant Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 3
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 2
- 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 2
- FRQQKWGDKVGLFI-UHFFFAOYSA-N 2-methylundecane-2-thiol Chemical compound CCCCCCCCCC(C)(C)S FRQQKWGDKVGLFI-UHFFFAOYSA-N 0.000 description 2
- VUTBELPREDJDDH-UHFFFAOYSA-N 4-amino-5-hydroxymethyl-2-methylpyrimidine Chemical compound CC1=NC=C(CO)C(N)=N1 VUTBELPREDJDDH-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
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 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
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N alpha-ketodiacetal Natural products O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000012662 bulk polymerization Methods 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- GNWBLLYJQXKPIP-ZOGIJGBBSA-N (1s,3as,3bs,5ar,9ar,9bs,11as)-n,n-diethyl-6,9a,11a-trimethyl-7-oxo-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydro-1h-indeno[5,4-f]quinoline-1-carboxamide Chemical compound CN([C@@H]1CC2)C(=O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H](C(=O)N(CC)CC)[C@@]2(C)CC1 GNWBLLYJQXKPIP-ZOGIJGBBSA-N 0.000 description 1
- YTLYLLTVENPWFT-UPHRSURJSA-N (Z)-3-aminoacrylic acid Chemical compound N\C=C/C(O)=O YTLYLLTVENPWFT-UPHRSURJSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- YKNKBBMRKMLLJS-UHFFFAOYSA-N 1-phenylaziridine Chemical compound C1CN1C1=CC=CC=C1 YKNKBBMRKMLLJS-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- FXWFZIRWWNPPOV-UHFFFAOYSA-N 2-aminobenzaldehyde Chemical compound NC1=CC=CC=C1C=O FXWFZIRWWNPPOV-UHFFFAOYSA-N 0.000 description 1
- VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 description 1
- XSXYESVZDBAKKT-UHFFFAOYSA-N 2-hydroxybenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1O XSXYESVZDBAKKT-UHFFFAOYSA-N 0.000 description 1
- GUXJXWKCUUWCLX-UHFFFAOYSA-N 2-methyl-2-oxazoline Chemical compound CC1=NCCO1 GUXJXWKCUUWCLX-UHFFFAOYSA-N 0.000 description 1
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
- ZXTHWIZHGLNEPG-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1 ZXTHWIZHGLNEPG-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- ZWENZDHVANLDQS-UHFFFAOYSA-N 4-(aziridine-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CC1 ZWENZDHVANLDQS-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- CUXGDKOCSSIRKK-UHFFFAOYSA-N 7-methyloctyl prop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C=C CUXGDKOCSSIRKK-UHFFFAOYSA-N 0.000 description 1
- DEVXQDKRGJCZMV-UHFFFAOYSA-K Aluminum acetoacetate Chemical compound [Al+3].CC(=O)CC([O-])=O.CC(=O)CC([O-])=O.CC(=O)CC([O-])=O DEVXQDKRGJCZMV-UHFFFAOYSA-K 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 102100026735 Coagulation factor VIII Human genes 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920001744 Polyaldehyde Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 description 1
- YBCVMFKXIKNREZ-UHFFFAOYSA-N acoh acetic acid Chemical compound CC(O)=O.CC(O)=O YBCVMFKXIKNREZ-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 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
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000001541 aziridines Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 238000009835 boiling Methods 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
- 239000001273 butane Substances 0.000 description 1
- SKGVGRLWZVRZDC-UHFFFAOYSA-N butyl 2-sulfanylacetate Chemical compound CCCCOC(=O)CS SKGVGRLWZVRZDC-UHFFFAOYSA-N 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 125000002704 decyl group Chemical group [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])* 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- YTQHSQQSLTYMSL-UHFFFAOYSA-N dodecanohydrazide Chemical compound CCCCCCCCCCCC(=O)NN YTQHSQQSLTYMSL-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- ALPIESLRVWNLAX-UHFFFAOYSA-N hexane-1,1-dithiol Chemical compound CCCCCC(S)S ALPIESLRVWNLAX-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 229960004251 hydroquinine Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- ZUHZZVMEUAUWHY-UHFFFAOYSA-N n,n-dimethylpropan-1-amine Chemical compound CCCN(C)C ZUHZZVMEUAUWHY-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- MDYPDLBFDATSCF-UHFFFAOYSA-N nonyl prop-2-enoate Chemical compound CCCCCCCCCOC(=O)C=C MDYPDLBFDATSCF-UHFFFAOYSA-N 0.000 description 1
- QJAOYSPHSNGHNC-UHFFFAOYSA-N octadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCCCS QJAOYSPHSNGHNC-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 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
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- DYFXGORUJGZJCA-UHFFFAOYSA-N phenylmethanediamine Chemical compound NC(N)C1=CC=CC=C1 DYFXGORUJGZJCA-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 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
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 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
- C09J201/00—Adhesives based on unspecified macromolecular compounds
-
- 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
- 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
- C09J133/062—Copolymers with monomers not covered by C09J133/06
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/28—Non-macromolecular organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
Definitions
- the present invention relates to a water-dispersed pressure-sensitive adhesive composition having excellent balance between water resistance and adhesive strength, balance between moisture resistance and adhesive strength, balance between cohesive strength and adhesive strength, and excellent substrate adhesion.
- the present invention relates to a production method and a pressure-sensitive adhesive product using the same. Background art
- the line-up of pressure-sensitive adhesives can be supplied from solvent type (using organic solvent as solvent) to solventless type. (Using no organic solvent) has become a major trend.
- solvent type using organic solvent as solvent
- solventless type Using no organic solvent
- water-dispersed, so-called emulsion-type pressure-sensitive adhesives are particularly preferably used among solvent-free types.
- the water-dispersed pressure-sensitive adhesive requires a dispersant such as an emulsifier in order to disperse the pressure-sensitive adhesive polymer in an aqueous medium. Since this dispersant is a water-soluble substance, There is a major problem that the water resistance of the pressure-sensitive adhesive is inferior to that of the solvent type.
- Japanese Patent Application Laid-Open No. 1222402 by the applicant of the present application discloses that a water-dispersed pressure-sensitive adhesive using a polymer having a specific structure as an emulsifier has an adhesive property, water resistance and moisture resistance.
- a monomer having a functional group capable of reacting with the carboxyl group of the dispersant as a monomer for a pressure-sensitive adhesive polymer.
- the emulsifier reacts with the pressure-sensitive adhesive polymer to further improve the water resistance. Is described.
- Japanese Patent Application Laid-Open No. 1-2221402 is not yet satisfactory.
- the inventors of the present application continued to study to improve the water resistance, but simply increasing the content of the functional group in the pressure-sensitive adhesive polymer reduced the adhesive strength and caused a difference in water resistance and adhesive strength. This is not preferred because it causes a problem in the performance and lowers the polymerization stability.
- Japanese Patent Publication No. 2-33432 discloses a pressure-sensitive adhesive water dispersion synthesized by emulsion polymerization using an emulsifier having a functional group capable of reacting with an isocyanate group.
- the pressure-sensitive adhesive of this invention is said to have excellent adhesive strength and moisture-resistant holding power.
- the functional group of the emulsifier reacts with the isocyanate compound in the form of aqueous dispersion, the two are reacted until the isocyanate group is no longer detected. More than holding the state Must still remain high in hydrophilic groups in the emulsifier.
- the pressure-sensitive adhesive of the present invention is described as having excellent adhesive strength and moisture-resistant holding power.
- the moisture-resistant holding power is a value measured at a level of at most 65% humidity. Judging from the severe water resistance test such as immersion in water, the value was obtained under fairly mild conditions, and could not be said to be very excellent in “water resistance”. Furthermore, since the isocyanate group has a very high reactivity with water, it is also consumed by water, which is a dispersion medium, so that the reproducibility of performance such as adhesive strength and moisture resistance can be reduced. Was also prone to problems.
- a water-dispersed pressure-sensitive adhesive composition capable of significantly improving the water resistance of a water-dispersed pressure-sensitive adhesive and exhibiting the same or higher level of water resistance as a solvent-type pressure-sensitive adhesive composition.
- a pressure-sensitive adhesive product that is excellent in water resistance, moisture resistance, balance between cohesive strength and adhesive strength, and has good substrate adhesion.
- Compound (B) is selected from the group consisting of a carboxyl group, an amino group, a glycidyl group, an aziridinyl group, an acetoacetyl group, an oxazolinyl group, a mercapto group, a hydrazide group and an aldehyde group. It is a preferred embodiment of the composition of the present invention that the compound [B-2] has at least one kind of functional group selected in its molecule.
- the compound [B] can also be referred to as a trapping agent for capturing a functional group of the dispersant [C], or a capping agent for blocking the functional group.
- the compound [B] and the dispersant [C] do not substantially react with each other in the state of the water dispersion, and the composition is coated.
- the reaction between the compound [B] and the dispersant [C] occurs when or after drying to disperse the water. Therefore, in the state of an aqueous dispersion, the stable dispersion state is maintained by the hydrophilic functional group of the dispersant [C], and when the product is used as a pressure-sensitive adhesive product after coating and drying, it is dispersed. Since all the hydrophilic functional groups of the agent [C] have been hydrophobized by the compound [B], they exhibit extremely excellent water resistance.
- a polymerizable monomer which is a raw material of the pressure-sensitive adhesive polymer [A] in the presence of water and the dispersant [C] is used.
- One example is a method in which a body component is polymerized and obtained by adding a compound [B]. After synthesizing the pressure-sensitive adhesive polymer [A] and dispersing it in water using a dispersant [C], the compound
- the method of adding [B] can also be adopted.
- the pressure-sensitive adhesive product of the present invention comprises a pressure-sensitive adhesive polymer (A),
- a water-dispersible pressure-sensitive adhesive obtained by polymerizing a polymerizable monomer component as a raw material of the pressure-sensitive adhesive polymer [A] in the presence of water and the dispersant [C], and then adding the compound [B].
- a preferred embodiment is a pressure-sensitive adhesive product provided with a pressure-sensitive adhesive layer using the agent composition.
- a pressure-sensitive adhesive product comprising a pressure-sensitive adhesive layer, wherein the pressure-sensitive adhesive layer substantially comprises a pressure-sensitive adhesive polymer (A), the compound (B), and the compound A film composed of a water-dispersible pressure-sensitive adhesive composition containing a dispersant (C) having a functional group that reacts with (B), wherein the compound (B) reacts with the dispersant (C) to form a dispersant.
- the present invention also includes a pressure-sensitive adhesive product whose hydrophilicity has been reduced.
- the present invention relates to a compound (B) capable of reacting a hydrophilic functional group of a dispersant (C) used for converting a pressure-sensitive adhesive polymer (A) into an aqueous dispersion with the functional group.
- the characteristic is that the hydrophilicity of the dispersant [C] is lost by the reaction, and the water resistance of the pressure-sensitive adhesive can be remarkably improved.
- the present invention will be described in detail.
- the pressure-sensitive adhesive polymer (A) which is an essential component of the water-dispersed pressure-sensitive adhesive composition of the present invention, is generally referred to as a pressure-sensitive adhesive in a temperature range where a pressure-sensitive adhesive product is used.
- Any polymer can be used without particular limitation as long as it is a polymer that can exhibit water dispersion without being dissolved in water.
- a polymer mainly composed of alkyl polyacrylate, natural rubber, styrene-isoprene-styrene (SIS) block copolymer, styrene-butadiene Diene styrene (SBS) block copolymers and other synthetic rubbers are examples of the most easily available pressure-sensitive adhesive polymers.
- alkyl with 4 to 14 carbon atoms A polymer of a monomer component essentially containing at least one (meth) alkyl acrylate monomer having a group and at least one monomer having a solubility parameter of 11 or more. It is preferable to use it as the pressure-sensitive adhesive polymer [A].
- the solubility parameter for example, the calculation method and the calculated value are described in Chapter II ( ⁇ 39 or later) of “Plastic Paint Printing Handbook”.
- Alkyl (meta) acrylates with alkyl groups of 4 to 14 carbon atoms Specific examples of the ester monomer include (meth) butyl acrylate, (meth) amino acrylate, (meth) acrylic acid heptyl ester, (Meth) acrylinoleic acid 2—ethylhexyl, (meth) acrylinoleic acid n—methyl octyl, (meth) isooctyl acrylate, (meth) nonyl acrylate, (meta) ) Isononyl acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, tridecyl (meth) acrylate, and one or more of these may be used.
- (meth) acrylic acid alkyl esters are preferably used in an amount of 50% by weight or more of all the monomer components constituting the pressure-sensitive adhesive polymer [A]. If the amount is less than 50% by weight, it is difficult to obtain good adhesive properties.
- monomers having a solubility parameter of 11 or more include N, N—dimethylaminorea, acrylamide, methanorea, and N—isopropylaque. Lilamide, N—vinylpyrrolidone, 2-hydroxyhydroxymethyl acrylate, 2—hydroxymethylic methacrylate, N, N—dimethylaminoethyl (meth) acrylate No.
- solubility parameters of the monomers for example, the calculation method and the calculated values are described in Chapter II of the “Plastic Painting and Printing Handbook” (P39 and after).
- these monomers are preferably contained in an amount of 0.1% by weight or more based on all the monomer components constituting the pressure-sensitive adhesive polymer [A]. It is preferable to use an unsaturated monomer having a solubility parameter of at least 1 1 1 as an essential component because a balance between water resistance and tackiness can be easily obtained.
- the upper limit of the solubility parameter is preferably 15 or less in consideration of the adhesive property.
- Acrylic esters aromatic unsaturated hydrocarbons such as styrene and n-methylstyrene; aliphatic unsaturated hydrocarbons such as ethylene and butadiene; vinyl esters such as vinyl acetate; Vinyl ethers such as tyl vinyl ether; and unsaturated cyanide compounds such as acrylonitrile.
- a functional group capable of reacting with the functional group of compound [B] or dispersant [C] must be used (meta).
- all three components such as the pressure-sensitive adhesive polymer [A], the compound [B] and the dispersant [C] can be crosslinked.
- the adhesiveness may decrease slightly due to bonding.
- any amount may be used as long as the amount does not impair the adhesiveness.
- the Tg (glass transition temperature) of the pressure-sensitive adhesive polymer [A] is preferably in the range of -70 ° C to 120 ° C. Note that T g (K) is calculated by the following equation.
- the T g (K) pressure-sensitive adhesive polymer [A] of a homopolymer of each monomer a conventionally known method can be used. Polymerization method, suspension polymerization method, bulk polymerization method, solution polymerization method, etc.
- the pressure-sensitive adhesive polymer [A] is an aqueous dispersion
- the method of synthesis by the emulsion polymerization method is most preferred. It is simple.
- an aqueous dispersion may be formed using the dispersant [C].
- any conventionally known emulsion polymerization method can be applied.
- a method in which a dispersant [C] described below is used as an emulsifier, and a polymerization initiator, deionized water, and monomers are mixed and polymerized at one time or a monomer sequential addition polymerization method, Methods such as a monomer emulsion polymerization method and a seed polymerization method can be applied.
- the polymerization temperature is from 0 to 100 ° C, preferably from 50 to 90, and the preferred polymerization time is from 1 to 10 hours.
- Addition of a hydrophilic solvent or addition of a known emulsifier other than the dispersant (C) during emulsion polymerization does not adversely affect the performance of the water-dispersed pressure-sensitive adhesive composition of the present invention. It is possible in the range.
- the initiator for emulsion polymerization examples include inorganic peroxides such as ammonium persulfate, potassium persulfate, and hydrogen peroxide; organic peroxides such as t-butyl hydroperoxide and succinic baroxide: azobis Water-soluble azo compounds, such as cyanovaric acid, can be used. Also, these peroxides can be used as a redox initiator in combination with a reducing agent such as sodium sulfite, sodium formaldehyde sulfoquinate, and ascorbic acid. An alkyl mercaptan such as dodecylmercaptan may be used as a molecular weight regulator so that the molecular weight is not excessively increased during polymerization.
- inorganic peroxides such as ammonium persulfate, potassium persulfate, and hydrogen peroxide
- organic peroxides such as t-butyl hydroperoxide and succinic baroxide:
- a dispersant (C) for stably dispersing the pressure-sensitive adhesive polymer (A) in water.
- the compound [B] is a trapping agent for the hydrophilic functional group of the dispersant [C] or a capping agent for blocking the functional group. It can be said.
- Compound (B) comprises a carboxyl group, an amino group, a glycidyl group, an aziridinyl group, an acetoacetyl group, an oxazolinyl group, a mercapto group, a hydrazide group, and an aldehyde group in the molecule. It is a compound containing at least one functional group selected from the group, or a metal-containing compound having two or more valences.
- Compound [B] is a compound having only one functional group selected from the above-mentioned functional groups in the molecule [compound [B-1]] and a compound having two or more functional groups described above. [B-2] and di- or higher valent metal-containing compounds [B-3].
- the monofunctional compound [B-1] loses hydrophilicity by capturing one of the hydrophilic functional groups of the dispersant [C] by reacting with the dispersant [C]. Since the polyfunctional compound [B-2] is capable of reacting with two or more molecules of the dispersant [C], the dispersant [C] is substantially combined with the dispersant [C-2] via the compound [B-2]. The molecular weight of the dispersant [C] increases. As the molecular weight of the dispersant [C] increases, the hydrophobicity increases, and the effect of capturing a hydrophilic group is added, whereby the hydrophilicity of the dispersant [C] can be more reliably lost.
- the functional groups of the compound [B-2] may be the same or different.
- the divalent or higher valent metal-containing compound [B-3] has the same effect as the compound [B-2]. Therefore, of the compound [B], the compound [B-2] or the metal-containing compound [B-3] is more preferably used than the compound [B-1
- Examples of the compound [B-1] include the following.
- Compound containing a lipoxyl group
- Aliphatic amines such as butylamine, aromatic amines such as phenylamine
- Aliphatic oxides such as propylene oxide, aromatic oxides such as styrene oxide, alicyclic epoxides such as cyclohexenoxide, butyl dalicydyl ether, “Evolite M—1 230 (Manufactured by Kyoeisha Yushi Kagaku Kogyo Co., Ltd.), aromatic glycidyl ethers such as phenyldaricidyl ether, and glycidyl esters such as glycidyl (meth) acrylate. etc.
- Aliphatic aziridines such as butylradizine, aromatic aziridines such as phenylaziridin, and unsaturated aziridines such as 2-((1-aziridinyl) ethylmethacrylate)
- Alkyl acetates such as ethyl acetate, and aromatic acetates such as acetate acetate
- aliphatic mercaptans such as hexylmercaptan, aromatic mercaptans such as thiophenol, alkyl mercaptoacetates such as butyl thioglycolate, 1-methyl-5-mercapto-11, 2, 3, 4-heterocyclic mercaptans such as tetrazole Hydrazide group-containing compounds:
- Aliphatic hydrazides such as lauric hydrazide, aromatic hydrazides such as salicylic hydrazide, and heterocyclic hydrazides such as pyrazole
- n Aliphatic aldehydes such as hexyl aldehyde, aromatic aldehydes such as benzaldehyde, etc.
- Examples of the compound [B-2] include the following compounds.
- Aliphatic polycarboxylic acids such as dodecane diacid, aromatic polycarboxylic acids, copolymers of carboxyl group-containing unsaturated monomers (acrylic acid, etc.), etc.
- Aliphatic polyamines such as triethylenetetramine, alicyclic polyamines such as isophorone diamine, and aromatic polyamines such as diamino phenylmethane Products, polyamides, Nippon Shokubai's “Polyment” series, etc.
- Polyglycidylamines such as “TET RAD” series manufactured by Mitsubishi Gas Chemical Co., Ltd.
- polyglycidyl ethers such as “Denacol” series manufactured by Nagase Corporation
- Aliphatic polymercap compounds such as dimercaptohexane, aromatic polymercap compounds such as triazine thiol compounds, etc.
- Dialdehydes such as glyoxal and terephthalaldehyde, and polyaldehydes such as copolymers of acrolein
- Examples of the compound [B-2] containing different functional groups include amino acids such as glycine and phenylalanine having a carboxyl group and an amino group, and carboxylic acid groups such as carboxyl group and mercapbu.
- Carboxyl group such as acetylglycin thioglycolate having amino group, amino thiophenol having amino group and mercapto group, aminobenz aldehyde having amino group and aldehyde group, etc.
- a hydrazide group-containing hydrazinoimidazole-4 (or 5) -propionic acid are examples of the compound [B-2] containing different functional groups.
- Examples of the divalent or higher valent metal-containing compound [B-3] include metal oxides such as zinc oxide, which is an oxide of a divalent metal, and trifluoroacetate chromium acetate, which is a salt of a divalent metal.
- Metal chelates such as aluminum salt (acetyl acetate), which is a chelate for metal salts and trivalent metals, and zircosol, a chelate for tetravalent metals, manufactured by Daiichi Rare Element Chemicals Co., Ltd.
- Examples thereof include compounds, metal halides such as zinc chloride which is a halide of a divalent metal, and the like.
- Dispersant (C) another essential component in the composition of the present invention, is A functional group capable of reacting with the functional group contained in the compound [B-1] or the compound [B-2] or a metal atom of the divalent or higher valent metal compound [B-3];
- the pressure-sensitive adhesive polymer [A] can be dispersed in water.
- a dispersant is a compound having both a hydrophobic (lipophilic) hydrocarbon group of a certain size and a hydrophilic group for imparting dispersion stability in one molecule, and a surfactant or an emulsifier. It can also be said.
- the functional group or metal atom in the compound [B] is chemically bonded to a large number of hydrophilic functional groups of the dispersing agent [C] to form the hydrophilicity of the dispersing agent [C].
- the hydrophilic functional group in the dispersant [C] has a reactivity with the compound [B] and stabilizes the pressure-sensitive adhesive polymer [A]. There is no particular limitation as long as it can be dispersed in water.
- Specific examples of the combination of the functional group of the compound [B] and the functional group of the dispersant [C] capable of reacting with the functional group include carboxyl group and glycidyl group, carboxyl group and amino group, and carboxyl group.
- the former is an example of the functional group of the compound [B].
- the number of functional groups of the dispersant [C] is not limited to one, and the actual combination of the functional groups of the compound [B] and the dispersant [C] will be various.
- the most preferred combination is that compound [B] has at least glycidyl groups and dispersant [C] has at least carboxyl groups, or compound [B] has at least aziridyl. In this case, the dispersant [C] has at least a carboxyl group.
- N-acylamino acids and salts thereof Fatty acid properties, N-acylamino acids and salts thereof, alkyl ether carboxylic acids (eg, “MX-RLM Series J” manufactured by Kao Corporation), etc., acylated peptides, carboxybetaine type Surfactants, aminocarboxylates, and polycarboxylic acid type polymer surfactants (for example, “Latemul”, “Demol”, “Voise”, “Homogenol” manufactured by Kao Corporation) Lease, etc.)
- a polymerizable monomer component containing an unsaturated carboxylic acid as an essential component is polymerized in the presence of an alkylmercaptane having 6 to 18 carbon atoms. It is also a preferred embodiment to use a water-soluble or water-dispersible polymer (c) having an acid value of 200 or more and / or a salt thereof. This is because it has excellent dispersion stability and further improves the water resistance of the pressure-sensitive adhesive.
- the unsaturated carboxylic acid used as an essential component when synthesizing the polymer for a dispersant (C) include (meth) acrylic acid, crotonic acid, maleic acid, and fumaric acid. Or itaconic acid or a half-ester of a dibasic acid thereof or a salt thereof;
- One or a mixture of two or more can be used.
- the polymerizable monomer component for synthesizing the polymer (c) may be composed of only unsaturated carboxylic acid, but if necessary, a monomer other than unsaturated carboxylic acid may be used in combination. Is also good.
- styrene derivatives such as styrene, vinyl toluene, ⁇ -methinorestyrene, chlormethinorestyrene, styrene sulfonic acid and salts thereof; (meta) acrylamide, ⁇ -Monomethyl (meta) acrylamide, ⁇ —monoethyl (meta) acrylylamide, ⁇ .
- (meta) acrylylamide such as dimethyl (meta) acrylylamide
- (Meth) acrylic acid such as (meth) methyl acrylate, (meth) ethyl acrylate, (meth) butyl acrylate, etc.
- the polymerizable monomer other than the unsaturated carboxylic acid is preferably used in such an amount that the acid value of the obtained polymer (c) does not become less than 200. Further, when the pressure-sensitive adhesive polymer [ ⁇ ] is emulsion-polymerized using the obtained polymer (c) as a dispersant, or in water, the pressure-sensitive adhesive polymer [ ⁇ ] is used. It is preferable to select the type and amount of the monomer other than the unsaturated force rubonic acid in consideration of the compatibility with the polymer [A] when dispersing the polymer, and synthesize the polymer (c). New
- alkylmenolecaptan having 6 to 18 carbon atoms in the alkyl group for synthesizing the polymer (c) examples include n-hexylmercaptan, n-octylmenolecaptan, and n-dodecylmercaptan. Examples thereof include butane, cetinolemenolecaptan, and stearylmercaptan, and one or a mixture of two or more of these can be used.
- Alkyl mercaptane is used to introduce an alkyl group into the terminal of the polymer (c) to impart surface activity.
- Alkyl mercaptane having an alkyl group of less than 6 carbon atoms is used for surface active activity.
- the function is too low to use.
- the alkylmercaptane is used in an amount of 2 to 300 parts by weight based on 100 parts by weight of the monomer constituting the polymer (c). If the amount is less than 2 parts by weight or more than 300 parts by weight, the surface activity of the dispersing agent [C] becomes poor, which is not preferable.
- a well-known oil-soluble or water-soluble polymerization initiator can be used, but in order to efficiently produce the polymer (c) having a terminal alkyl group, the amount used is limited to an alkyl.
- the ratio is preferably 1 mol or less, more preferably 0.1 mol or less, based on mercaptan.
- the polymer (c) can be produced by any method of bulk polymerization, solution polymerization, and suspension polymerization.
- the polymerization temperature is preferably 50 to 150 ° C, and the polymerization time is preferably 1 to 8 hours.
- any solvent can be used as long as the monomer component, alkylmercaptan, and radical polymerization initiator are dissolved and do not inhibit the radical polymerization.
- the polymer (c) itself has sufficient surface activity, a water-dispersed pressure-sensitive adhesive composition having good polymerization stability and storage stability can be obtained.
- a normal alkali compound can be used.
- sodium hydroxide, alkaline hydroxide metal such as hydroxide hydroxide, etc.
- Metal compounds calcium hydroxide, carbonate Alkaline earth metal compounds such as calcium; ammonia; monomethylamine, dimethylamine, trimethylamine, monoethylamine, getylamine, triethylamine, monopro Water-soluble organic compounds such as pyramin, dimethylpropylamin, monoethanolamine, diethanolamine, triethanolamine, ethylenediamine, diethylamine, etc.
- Amines can be used, and one or a mixture of two or more selected from these groups can be used. If it is desired to further improve the water resistance of the dried film, it is necessary to reduce the amount of ammonia, monomethylamine, dimethylethylamine, trimethylamine, etc. It is preferred to use boiling amines.
- the first method is to form a water dispersion by mechanically stirring the three components of the pressure-sensitive adhesive polymer [A], the dispersant [C], and water, and then add the compound [B]. It is. That is, in this method, the polymerization method of the pressure-sensitive adhesive polymer [A] is not particularly limited.
- a monomer component which is a raw material of the pressure-sensitive adhesive polymer (A) is emulsion-polymerized in the presence of the dispersant (C) to obtain an aqueous dispersion, and then the compound (B) It is a method of adding.
- the second method is simpler and more suitable in terms of workability and work efficiency.
- the dispersant [C] is preferably used in an amount of 0.5 to 10 parts by weight based on 100 parts by weight of the pressure-sensitive adhesive polymer [A].
- the amount is less than 0.5 part by weight, it is difficult to stably disperse the pressure-sensitive adhesive polymer [A] in water.
- the dispersant [C] is used in an amount exceeding 10 parts by weight, the effect of adding the compound [B] is not preferable because the effect of improving the water resistance of the pressure-sensitive adhesive product is not sufficiently exhibited.
- the amount of the compound [B] used is preferably in the range of 0.1 to 10 equivalents to 1 equivalent of the functional group of the dispersant [C]. More preferably, it is 0.5 to 5 equivalents.
- the amount of the compound [B] is less than 0.1, most of the hydrophilic functional groups of the dispersant [C] remain, and the effect of improving the water resistance is not sufficiently exhibited. Conversely, if the compound [B] is used in an amount exceeding 10 equivalents, a large amount of the functional group of the compound [B] will remain, and the effect may be impaired, which is not preferred.
- the resulting water-dispersed pressure-sensitive adhesive composition is stored for a long period of time. Since the reaction with the dispersant [C] may proceed to deteriorate the dispersion stability, it is preferable to apply the compound [B] relatively quickly after compounding.
- the water-dispersed adhesive composition of the present invention contains a known tackifier, a wetting agent, a viscosity regulator, a viscosity modifier, a pH regulator, an antifoaming agent, a modifier, and a tackifier.
- Conventionally known additives such as pigments, colorants, fillers, antioxidants, ultraviolet absorbers, and ultraviolet stabilizers may be added within a range that does not adversely affect water resistance.
- tackifier examples include (polymerized) rosin type, (polymerized) rosin ester type, terpene type, terpene phenol type, coumarone type, coumaroneindene type and styrene.
- examples thereof include a lene resin type, a xylene resin type, a phenol resin type, and a petroleum resin type. Since most of these compounds are oil-soluble, they may be dissolved in an organic solvent and added directly to the water-dispersed pressure-sensitive adhesive composition of the present invention, but the dispersant (C) used in the present invention may be used. It is preferable to use a water-based dispersion of these tackifiers in a composition.
- the method for producing a pressure-sensitive adhesive product from the water-dispersed pressure-sensitive adhesive composition of the present invention is described below.
- the water-dispersed pressure-sensitive adhesive composition is applied to a base material to form a dried film, thereby obtaining a pressure-sensitive adhesive product.
- Examples of the pressure-sensitive adhesive product include a mode in which a pressure-sensitive adhesive layer is formed on one side of a support, a mode in which a pressure-sensitive adhesive layer is formed on both sides of a support, and a mode having no support.
- the water-dispersed pressure-sensitive adhesive composition is directly applied on the support and dried to obtain a pressure-sensitive adhesive.
- the product is obtained.
- the water-dispersed pressure-sensitive adhesive composition is applied to release paper and dried, a pressure-sensitive adhesive layer having no support can be formed.
- a pressure-sensitive adhesive layer having no support is formed and then transferred onto the support, a product in which the pressure-sensitive adhesive layer is formed on one side or both sides of the support can be obtained.
- the support it is preferable to use various materials generally used conventionally, such as paper, synthetic paper, plastic film, foam sheet, and non-woven cloth.
- the pressure-sensitive adhesive products obtained by the present invention include, for example, packaging tapes, masking tapes, industrial single-sided tapes, industrial double-sided tapes, paper labels, film labels, reflective sheets, protective sheets, It can be used in various forms in various fields, such as glass scattering prevention films, heat ray shielding films, medical adhesive products, and office adhesive products.
- water-dispersed pressure-sensitive adhesive composition of the present invention is used in the field of pressure-sensitive adhesives. Not only that, it can also be used for adhesives, paints, paper processing agents, textile processing agents, mortar modifiers, sealing agents, and the like.
- a flask equipped with a stirrer, a reflux condenser, a nitrogen inlet tube, a thermometer, and a dropping funnel was charged with 180 parts of isopropyl alcohol, and the internal temperature was increased to 81 ° C while blowing nitrogen. Isopropyl alcohol was refluxed for 10 minutes.
- 144 parts of acrylic acid prepared in advance, 28.3 parts of n-dodecylmercaptan, 33.6 parts of a mixture of lauric acid ridecyl acrylate and 33.6 parts of a polymerization initiator azobisisobutyl ester A polymerizable monomer mixture consisting of 0.22 parts of lonitrile was added dropwise over 2 hours to carry out polymerization.
- the mixture was aged for 1 hour under reflux to obtain a polymer solution having a solid content of 53.4%.
- Isopropyl alcohol was further removed under reduced pressure to obtain a dispersant [C-11] having a carboxyl group as a functional group.
- the acid value of the dispersant [C-11] was 544, and the number average molecular weight was 1,200.
- a flask equipped with a stirrer, reflux condenser, nitrogen inlet tube, thermometer, and dropping funnel was charged with 100 parts of isopropyl alcohol, and the internal temperature was raised to 81 ° C while blowing nitrogen. Then, isopropyl alcohol was refluxed for 10 minutes. Next, 27.3 isoprobe2 luxazoline, 17.3 parts, methyl polyethylene glycol acrylate (“AM_90G”: manufactured by Shin-Nakamura Chemical Co., Ltd.) 69 parts prepared in advance, n— Dodeci A polymerizable monomer mixture consisting of 13.7 parts of lumenorecaptan and 0.05 part of azobisisobutyronitrile was added dropwise over 1 hour to polymerize.
- the amount of the dispersant [C-11] obtained in Production Example 1 was 1.5 parts, the amount of tert-dodecylmercaptane was 0.03 parts, and the initiator was V-500.
- the polymerization reaction of the monomer components shown in Table 1 was carried out in the same manner as in Production Example 3 except that potassium persulfate was used in place of ⁇ 1 '', and an aqueous dispersion of the pressure-sensitive adhesive polymer [ CA-3]. The characteristic values are shown in Table 1.
- Production Example 6 (Production example of emulsion polymerization of pressure-sensitive adhesive polymer [A] using dispersant [C-11])
- Production Example 7 Example of emulsion polymerization of pressure-sensitive adhesive polymer [A] using dispersant [C_1])
- Production Example 8 Example of emulsion polymerization of pressure-sensitive adhesive polymer [A] using dispersant [C-12])
- an ether sulfate ammonium salt-based emulsifier (“HITENOL N-08”: Daiichi Pharmaceutical Co., Ltd.), which does not react with the compound [B], is used 2.
- the polymerization reaction of the monomer components shown in Table 1 was carried out in the same manner as in Production Example 3 except that 0 parts was used and the amount of tert-dodecylmercaptan was changed to 0.02 parts.
- An aqueous dispersion [A'-1] of a pressure-sensitive adhesive polymer was obtained.
- T g (° C) of the pressure-sensitive adhesive polymer obtained in each of the production examples was calculated from the T g (K) of the homopolymer of each monomer shown below and the above formula. Value.
- EHA 2—Ethylhexyl acrylate 20 3
- KDMAA N, N—Dimethylacrylorea amide 36 2
- KN V P n—Vinylpyrrolidone 448 K
- GMA Glycidyl methacrylate 3 14 K Manufacturing example Comparison
- Example 2 In the same manner as in Example 1, an aqueous dispersion of the pressure-sensitive adhesive polymer of the type and amount shown in Table 2 and the compound (B) were mixed and stirred, and the water-dispersed pressure-sensitive adhesive composition of the present invention was mixed. [2] to [10] were obtained.
- the aqueous dispersion [CA_1] of the pressure-sensitive adhesive polymer obtained in Production Example 3 was directly used as a comparative water-dispersible pressure-sensitive adhesive composition [12].
- the aqueous dispersion [CA-4] of the pressure-sensitive adhesive polymer obtained in Production Example 6 was directly used as a comparative water-dispersible pressure-sensitive adhesive composition [13].
- Aqueous dispersion of pressure-sensitive adhesive polymer obtained in Comparative Production Example 1 100 parts of the compound [B] of the type and amount shown in Table 2 were mixed and stirred to obtain a comparative water-dispersed pressure-sensitive adhesive composition [14].
- the functional group is a mercapto group.
- Each of the water-dispersed pressure-sensitive adhesive compositions obtained in Examples 1 to 10 and Comparative Examples 1 to 4 was coated on a 25 / zm-thick polyethylene terephthalate film by drying. the thickness was applied respectively so as to 2 5 / im, dried for 2 minutes in 1 0 5 e C hot air dryer, a release paper (K one 8 0 HS: manufactured by Kaken Kogyo) covered with an adhesive It was a tape. These adhesive tapes were aged in an atmosphere at a temperature of 23 ° C. and a humidity of 65% for at least one week, and then their adhesive properties were evaluated by the following method. Table 3 shows the results.
- composition [11] obtained in Example 11 was applied to a stretched polypropylene film which was coated with a release agent “RP15W” manufactured by Nippon Shokubai Co., Ltd. and subjected to release treatment.
- coating thickness is directly applied to be 2 5 im after drying, 1 0 in 5 e C hot air dryer after drying for 2 minutes, Po Li ethylene terephthalamide other thicknesses 2 5 // m
- the film was transferred to a latex film to form an adhesive tape.
- only the adhesive tape using the composition of Example 9 was dried at 120 ° C. for 30 minutes.
- the measuring method of each characteristic is as follows.
- the measurement was performed according to JISZ0237. Adhere an adhesive tape with a width of 25 mm and a length of about 150 mm on a stainless steel plate with an adhesion area of 25 mm and 25 mm, and fold the part without the adhesive tape inward, This is a test piece. The test piece was suspended vertically in a thermostat at 80 C, and then a load of 1 kg was suspended on the folded portion of the adhesive tape and left for 24 hours. The displacement distance (mm) after 24 hours or the time required to fall was measured.
- test piece was prepared in the same manner as the normal holding power, and immersed in water at 23 ° C for 24 hours. Immediately after removal from the water, the specimen is placed in a thermostat at 80 ° C. It was suspended vertically, suspended under a load of 1 kg, and allowed to stand for 24 hours.
- the holding power was evaluated by comparing the value of the holding power after immersion in water with that of the normal state.
- the adhesive strength was determined based on the following criteria.
- the weight of the adhesive tape piece cut into 25 mm x 70 mm is measured. Let this be W a. 2 3 with this piece of adhesive tape. C water 50 cc to 2 4 After immersion for a while, remove from the water, gently wipe off excess water on the surface, and weigh again. This is Wb. The weight of only the 25 mm X 7 O mm polyethylene terephthalate film is separately measured, and is represented by Wc. Using each weight, the water absorption was calculated by the following equation.
- Water absorption (%) [(Wb-Wa) / (Wa-Wc)] x 100 The determination of water absorption is less than 20% and less than 20% and less than 40%. , And 40% or more was defined as X.
- the pressure-sensitive adhesive tape obtained from the water-dispersed pressure-sensitive adhesive composition of the present invention has a balance between the holding power and the adhesive strength, as well as the water resistance, that is, the holding power after immersion in water, It is clear that all of these properties are excellent in adhesive strength, water absorption, and water whitening resistance.
- the comparative water-dispersed pressure-sensitive adhesive composition [12] does not contain the compound [B] that reacts with the carboxyl group of the dispersant [C]. Water resistance such as holding power after crushing, adhesive strength after immersion in water, water absorption, and water whitening resistance is remarkably inferior.
- the water-dispersible pressure-sensitive adhesive composition for comparison [13] also has poor water resistance because it does not contain the compound [B], but the dispersant [C] is contained in the pressure-sensitive adhesive polymer.
- the water-dispersed pressure-sensitive adhesive composition for comparison [14] uses a commercially available emulsifier having no functional group as a dispersant, so that even when compound [B] is combined, no response. It is considered that the compound [B] reacted with the functional group of the pressure-sensitive adhesive polymer [ ⁇ '-1], and the pressure-sensitive adhesive layer was considerably cross-linked. The adhesive strength is low, and the strength is low.
- the pressure-sensitive adhesive tape obtained from the water-dispersible pressure-sensitive adhesive composition for comparison [15] has a coronate having an isocyanate group as the compound [B] capable of reacting with the dispersant [C].
- the adhesive strength, water absorption, and water whitening resistance after immersion in water were poor.
- the water-dispersed pressure-sensitive adhesive composition of the present invention contains a pressure-sensitive adhesive polymer [A] and a functional group capable of reacting with the hydrophilic functional group of the dispersant [C]. And the dispersant (C) having a hydrophilic functional group, the dispersant (C) reacts with the functional group of the dispersant (C) and the functional group of the compound (B).
- the hydrophilic group of was able to be made hydrophobic. For this reason, when the composition of the present invention is formed into a dry film, remarkably improved water resistance is exhibited together with good adhesive strength.
- the pressure-sensitive adhesive product of the present invention has much better water absorption and water whitening resistance than products obtained from the conventional water-dispersed pressure-sensitive adhesive composition, and has a holding power and adhesive strength after immersion in water. No reduction was observed at all, and the level is comparable to the water resistance of the product obtained from the solvent-type pressure-sensitive adhesive composition without using an emulsifier. Therefore, even when used in a place where water resistance is required, the product of the present invention can be used in place of the product obtained from the solvent-type pressure-sensitive adhesive, and the work environment safety, This invention is extremely important and important in terms of global environmental protection and resource saving.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019960706585A KR100349459B1 (ko) | 1995-03-22 | 1996-03-21 | 수분산형감압접착제조성물,그제조방법및그것을사용한감압접착성제품 |
US08/737,590 US6121355A (en) | 1995-03-22 | 1996-03-21 | Water-dispersion type pressure-sensitive adhesive composition, method of production thereof, and pressure-sensitive adhesive product employing the same |
EP96906912A EP0763583B1 (en) | 1995-03-22 | 1996-03-21 | Water-dispersible pressure-sensitive adhesive composition, process for production thereof, and pressure-sensitive adhesive products made therefrom |
DE69626251T DE69626251T2 (de) | 1995-03-22 | 1996-03-21 | Wasserdispergierbare druckempfindliche klebstoffzusammensetzung, verfahren zu deren herstellung und daraus hergestellte druckempfindliche klebeartikel |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7/62966 | 1995-03-22 | ||
JP6296695 | 1995-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996029373A1 true WO1996029373A1 (fr) | 1996-09-26 |
Family
ID=13215594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1996/000740 WO1996029373A1 (fr) | 1995-03-22 | 1996-03-21 | Composition d'adhesif autocollant dispersable dans l'eau, son procede de production, et articles adhesifs autocollants fabriques a partir de cette composition |
Country Status (6)
Country | Link |
---|---|
US (1) | US6121355A (ja) |
EP (1) | EP0763583B1 (ja) |
KR (1) | KR100349459B1 (ja) |
DE (1) | DE69626251T2 (ja) |
TW (1) | TW440604B (ja) |
WO (1) | WO1996029373A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005200958A (ja) * | 2004-01-16 | 2005-07-28 | East Japan Railway Co | 土木構造物及び建築構造物の保護用シート及び該保護用シートを使用した保護方法 |
WO2006064747A1 (ja) * | 2004-12-15 | 2006-06-22 | Saitama Daiichi Pharmaceutical Co., Ltd. | 医療用テープ剤 |
JP2007056248A (ja) * | 2005-07-25 | 2007-03-08 | Nitto Denko Corp | 水分散型粘着剤組成物、粘着型光学フィルムおよび液晶表示装置 |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6518342B1 (en) | 1998-10-29 | 2003-02-11 | Nippon Shokubai Co., Ltd. | Emulsion for pressure-sensitive adhesive |
WO2002086007A1 (en) * | 2001-04-19 | 2002-10-31 | W.F. Taylor Co., Inc. | Low emissions one part adhesive |
US6686425B2 (en) * | 2001-06-08 | 2004-02-03 | Adhesives Research, Inc. | High Tg acrylic polymer and epoxy-containing blend therefor as pressure sensitive adhesive |
RU2418834C2 (ru) * | 2005-05-20 | 2011-05-20 | Эвери Деннисон Копэрейшн | Водостойкий акриловый чувствительный к давлению адгезивный полимер (варианты) и этикетка на его основе (варианты) |
US20110293834A1 (en) * | 2007-08-15 | 2011-12-01 | Allen David P | Thermal Activated Pressure Sensitive Adhesive and Method for Producing the Same and Product therewith |
US20090047514A1 (en) * | 2007-08-15 | 2009-02-19 | Allen David P | Thermal Activated Pressure Sensitive Adhesive and Method for Producing the Same and Product therewith |
JP4966398B2 (ja) * | 2009-08-05 | 2012-07-04 | ローム アンド ハース カンパニー | ウォッシュオフラベル |
TWI507495B (zh) * | 2011-01-18 | 2015-11-11 | Symbio Inc | 具有高黏著力與斬形特性之乳化型感壓黏著劑組成物及其應用 |
EP3303470B1 (en) | 2015-05-29 | 2019-09-18 | 3M Innovative Properties Company | Perfluoroelastomeric compositions comprising oxazoles |
CN109963909A (zh) * | 2016-08-01 | 2019-07-02 | 斯塔尔国际有限公司 | 乙醛释放量降低的聚合物分散体 |
JP6952494B2 (ja) * | 2017-05-25 | 2021-10-20 | 住友化学株式会社 | 接着剤組成物及び偏光板 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6424876A (en) * | 1987-07-20 | 1989-01-26 | Nichiban Kk | Self-adhesive composition |
JPH01221402A (ja) * | 1988-02-29 | 1989-09-04 | Nippon Shokubai Kagaku Kogyo Co Ltd | 粘着剤 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3890292A (en) * | 1973-05-23 | 1975-06-17 | Daubert Chemical Co | Adhesive compositions and tapes |
JPS50130829A (ja) * | 1974-04-05 | 1975-10-16 | ||
US4061611A (en) * | 1976-09-22 | 1977-12-06 | The Sherwin-Williams Company | Aqueous compositions containing starch ester dispersants |
US4250070A (en) * | 1978-01-26 | 1981-02-10 | Basf Aktiengesellschaft | Aqueous dispersions, containing hydrazine derivatives, of carbonyl-containing copolymers |
US4376844A (en) * | 1981-03-19 | 1983-03-15 | Rohm And Haas Company | Hydrocurable ambient curing polyepoxide coating and adhesive compositions and method of using them |
DE3402280C1 (de) * | 1984-01-24 | 1985-07-25 | Dynamit Nobel Ag, 5210 Troisdorf | Waermehaertbare Klebstoff- und Dichtungsmassen |
GB8412423D0 (en) * | 1984-05-16 | 1984-06-20 | Allied Colloids Ltd | Polymeric compositions |
WO1987002369A1 (en) * | 1985-10-11 | 1987-04-23 | Asahi Kasei Kogyo Kabushiki Kaisha | Terminal-modified block copolymer and composition containing said copolymer |
US4820863A (en) * | 1986-03-31 | 1989-04-11 | Union Carbide Corporation | Surface active polycarbodiimides |
US4735981A (en) * | 1986-10-03 | 1988-04-05 | Desoto, Inc. | Combinations of associative thickeners and aqueous latex paints containing the same |
US5116676A (en) * | 1987-04-15 | 1992-05-26 | Minnesota Mining And Manufacturing Company | Removable pressure-sensitive adhesive tape |
DE3720860A1 (de) * | 1987-06-24 | 1989-01-05 | Basf Ag | Lagerstabile waessrige polymerdispersionen |
JPH0757863B2 (ja) * | 1987-12-29 | 1995-06-21 | 日本合成化学工業株式会社 | 感圧性接着剤組成物 |
GB8811436D0 (en) * | 1988-05-13 | 1988-06-15 | Polyvinyl Chemie Holland Bv | Aqueous coating compositions |
US5147938A (en) * | 1991-04-02 | 1992-09-15 | Minnesota Mining And Manufacturing Company | Acrylate adhesives containing polymerizable fluorochemical surfactants |
JPH0641504A (ja) * | 1991-07-12 | 1994-02-15 | Saiden Kagaku Kk | アルカリ可溶型粘着剤組成物 |
CA2121355C (en) * | 1991-10-15 | 2002-09-17 | William Francis Scholz | Improvement in repulpable pressure-sensitive adhesive compositions |
US6251213B1 (en) * | 1992-10-01 | 2001-06-26 | Rohm And Haas Company | Laminating construction adhesive compositions with improved performance |
US5508367A (en) * | 1993-11-29 | 1996-04-16 | Adhesives Research, Inc. | Water-soluble pressure sensitive adhesive |
US5670557A (en) * | 1994-01-28 | 1997-09-23 | Minnesota Mining And Manufacturing Company | Polymerized microemulsion pressure sensitive adhesive compositions and methods of preparing and using same |
US5500470A (en) * | 1994-09-06 | 1996-03-19 | W.R. Grace & Co.-Conn. | Composition for utilizing synthetic polymer packages |
EP0743347B1 (en) * | 1995-05-15 | 2001-12-05 | Central Glass Company, Limited | Water-based fluorine-containing paint |
-
1996
- 1996-03-21 WO PCT/JP1996/000740 patent/WO1996029373A1/ja active IP Right Grant
- 1996-03-21 EP EP96906912A patent/EP0763583B1/en not_active Expired - Lifetime
- 1996-03-21 US US08/737,590 patent/US6121355A/en not_active Expired - Fee Related
- 1996-03-21 KR KR1019960706585A patent/KR100349459B1/ko not_active Expired - Fee Related
- 1996-03-21 DE DE69626251T patent/DE69626251T2/de not_active Expired - Fee Related
- 1996-03-26 TW TW085103588A patent/TW440604B/zh not_active IP Right Cessation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6424876A (en) * | 1987-07-20 | 1989-01-26 | Nichiban Kk | Self-adhesive composition |
JPH01221402A (ja) * | 1988-02-29 | 1989-09-04 | Nippon Shokubai Kagaku Kogyo Co Ltd | 粘着剤 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0763583A4 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005200958A (ja) * | 2004-01-16 | 2005-07-28 | East Japan Railway Co | 土木構造物及び建築構造物の保護用シート及び該保護用シートを使用した保護方法 |
WO2006064747A1 (ja) * | 2004-12-15 | 2006-06-22 | Saitama Daiichi Pharmaceutical Co., Ltd. | 医療用テープ剤 |
JPWO2006064747A1 (ja) * | 2004-12-15 | 2008-06-12 | 埼玉第一製薬株式会社 | 医療用テープ剤 |
US7976865B2 (en) | 2004-12-15 | 2011-07-12 | Nipro Patch Co., Ltd. | Medical tape preparation |
US8128946B2 (en) | 2004-12-15 | 2012-03-06 | Nipro Patch Co., Ltd. | Medical tape preparation |
JP5016309B2 (ja) * | 2004-12-15 | 2012-09-05 | ニプロパッチ株式会社 | 医療用テープ剤 |
KR101242834B1 (ko) | 2004-12-15 | 2013-03-12 | 니프로 패치 가부시키가이샤 | 의료용 테이프제 |
JP2007056248A (ja) * | 2005-07-25 | 2007-03-08 | Nitto Denko Corp | 水分散型粘着剤組成物、粘着型光学フィルムおよび液晶表示装置 |
Also Published As
Publication number | Publication date |
---|---|
KR970703400A (ko) | 1997-07-03 |
TW440604B (en) | 2001-06-16 |
US6121355A (en) | 2000-09-19 |
DE69626251T2 (de) | 2003-11-13 |
DE69626251D1 (de) | 2003-03-27 |
EP0763583A4 (en) | 1998-09-09 |
EP0763583A1 (en) | 1997-03-19 |
KR100349459B1 (ko) | 2005-04-06 |
EP0763583B1 (en) | 2003-02-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5121834B2 (ja) | 両面粘着テープ | |
JP3640921B2 (ja) | 合成樹脂エマルジョン、それを含んでなる易水膨潤性粘着剤組成物、および合成樹脂エマルジョンの製造方法 | |
KR20050067158A (ko) | 재부착가능하며,수-백화에 저항성이 있는 감압성 접착제 | |
WO1996029373A1 (fr) | Composition d'adhesif autocollant dispersable dans l'eau, son procede de production, et articles adhesifs autocollants fabriques a partir de cette composition | |
CN102471658B (zh) | 水性粘结剂组合物、其制备方法及粘结薄膜 | |
EP0797644A1 (en) | Removable pressure sensitive adhesive and article | |
EP0913443A1 (en) | Heat-sensitive and pressure-sensitive adhesive sheet | |
WO1991018739A1 (en) | Water-borne acrylic emulsion pressure sensitive latex adhesive composition | |
JP3568671B2 (ja) | 水性接着剤組成物 | |
JP2002080809A (ja) | 水性エマルジョン型感圧接着剤 | |
JP3834262B2 (ja) | 水性エマルジョン型粘着剤および粘着シート | |
JPH10330693A (ja) | 結露面または湿潤面に対する感圧接着方法および該方法に用いられる水分散型感圧接着剤組成物 | |
JPS6328949B2 (ja) | ||
JP4225388B2 (ja) | 発泡体用水性エマルジョン型粘着剤 | |
JP3535780B2 (ja) | 感圧接着剤用エマルション | |
US20200392381A1 (en) | Polymer additives for pressure-sensitive adhesives | |
JPH0665551A (ja) | 水性感圧接着剤組成物 | |
JP5512119B2 (ja) | アクリルエマルション粘着剤 | |
JPH0456071B2 (ja) | ||
JP2005194448A (ja) | 粘着剤用アクリル系共重合体エマルション及び該エマルションの製造方法、並びに粘着シート | |
JP3611911B2 (ja) | アクリル系エマルジョン型粘着剤 | |
JPH0860117A (ja) | 架橋型アクリル系感圧接着剤 | |
CN114846105A (zh) | 丙烯酸类乳液压敏粘合剂组合物 | |
JPH0465879B2 (ja) | ||
JPH0819395B2 (ja) | 転写塗工が可能な再剥離型粘着剤組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): JP KR US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1019960706585 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 08737590 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1996906912 Country of ref document: EP |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWP | Wipo information: published in national office |
Ref document number: 1996906912 Country of ref document: EP |
|
WWG | Wipo information: grant in national office |
Ref document number: 1996906912 Country of ref document: EP |