JP2005220294A - Adhesive composition - Google Patents
Adhesive composition Download PDFInfo
- Publication number
- JP2005220294A JP2005220294A JP2004031705A JP2004031705A JP2005220294A JP 2005220294 A JP2005220294 A JP 2005220294A JP 2004031705 A JP2004031705 A JP 2004031705A JP 2004031705 A JP2004031705 A JP 2004031705A JP 2005220294 A JP2005220294 A JP 2005220294A
- Authority
- JP
- Japan
- Prior art keywords
- emulsion
- adhesive composition
- weight
- parts
- polymerizable unsaturated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000853 adhesive Substances 0.000 title claims abstract description 86
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 86
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 239000000839 emulsion Substances 0.000 claims abstract description 69
- 239000000178 monomer Substances 0.000 claims abstract description 44
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 38
- 239000000057 synthetic resin Substances 0.000 claims abstract description 38
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 claims abstract description 30
- 150000001875 compounds Chemical group 0.000 claims abstract description 26
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229920001567 vinyl ester resin Polymers 0.000 claims abstract description 19
- 150000004676 glycans Chemical class 0.000 claims abstract description 17
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 17
- 239000005017 polysaccharide Substances 0.000 claims abstract description 17
- 239000000084 colloidal system Substances 0.000 claims abstract description 15
- 238000007720 emulsion polymerization reaction Methods 0.000 claims abstract description 15
- 230000001681 protective effect Effects 0.000 claims abstract description 15
- 239000011342 resin composition Substances 0.000 claims abstract description 9
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 24
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 19
- 238000002156 mixing Methods 0.000 claims description 16
- 239000002023 wood Substances 0.000 claims description 12
- 239000011120 plywood Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 125000004185 ester group Chemical group 0.000 claims description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 27
- 238000009835 boiling Methods 0.000 abstract description 5
- 239000003960 organic solvent Substances 0.000 abstract description 4
- 238000011109 contamination Methods 0.000 abstract 1
- 230000007613 environmental effect Effects 0.000 abstract 1
- 230000007774 longterm Effects 0.000 abstract 1
- 229920001290 polyvinyl ester Polymers 0.000 abstract 1
- -1 isocyanate compound Chemical class 0.000 description 24
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 20
- 239000012948 isocyanate Substances 0.000 description 16
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
- 150000003254 radicals Chemical class 0.000 description 13
- 239000011122 softwood Substances 0.000 description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000000499 gel Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000013329 compounding Methods 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 238000003825 pressing Methods 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000003822 epoxy resin Substances 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 150000005846 sugar alcohols Polymers 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
- 229920003169 water-soluble polymer Polymers 0.000 description 4
- DGXAGETVRDOQFP-UHFFFAOYSA-N 2,6-dihydroxybenzaldehyde Chemical compound OC1=CC=CC(O)=C1C=O DGXAGETVRDOQFP-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000003912 environmental pollution Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000011121 hardwood Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 244000215068 Acacia senegal Species 0.000 description 2
- 241000218631 Coniferophyta Species 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
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920000084 Gum arabic Polymers 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000000205 acacia gum Substances 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003786 synthesis reaction Methods 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
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- AUIWZRLALNEDGC-UHFFFAOYSA-N (2-methylprop-2-enoylamino)methyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCNC(=O)C(C)=C AUIWZRLALNEDGC-UHFFFAOYSA-N 0.000 description 1
- DDKMFQGAZVMXQV-UHFFFAOYSA-N (3-chloro-2-hydroxypropyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CCl DDKMFQGAZVMXQV-UHFFFAOYSA-N 0.000 description 1
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- IOOZKHMFNNJCMG-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)propan-2-yl 3-oxobutanoate Chemical compound CC(=C)C(=O)OCC(C)OC(=O)CC(C)=O IOOZKHMFNNJCMG-UHFFFAOYSA-N 0.000 description 1
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 description 1
- NGZDFOYYIXAAPC-UHFFFAOYSA-N 1-prop-2-enoyloxypropan-2-yl 3-oxobutanoate Chemical compound C=CC(=O)OCC(C)OC(=O)CC(C)=O NGZDFOYYIXAAPC-UHFFFAOYSA-N 0.000 description 1
- CRRYHGFIJXAGHN-UHFFFAOYSA-N 2-(2-methylprop-2-enoylamino)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCNC(=O)C(C)=C CRRYHGFIJXAGHN-UHFFFAOYSA-N 0.000 description 1
- CZVMDPUTEUXCPK-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 2-cyano-3-oxobutanoate Chemical class CC(=O)C(C#N)C(=O)OCCOC(=O)C(C)=C CZVMDPUTEUXCPK-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
- RUYYZQCJUGZUCW-UHFFFAOYSA-N 2-(prop-2-enoylamino)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCNC(=O)C=C RUYYZQCJUGZUCW-UHFFFAOYSA-N 0.000 description 1
- QYVVXYNXJQERRN-UHFFFAOYSA-N 2-hydroxyethyl 2-methylprop-2-enoate;2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C.CC(=C)C(=O)OCCO QYVVXYNXJQERRN-UHFFFAOYSA-N 0.000 description 1
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- XLLXMBCBJGATSP-UHFFFAOYSA-N 2-phenylethenol Chemical compound OC=CC1=CC=CC=C1 XLLXMBCBJGATSP-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- ZGLJYJVYUYQOHR-UHFFFAOYSA-N 3-oxobutanoyl 4-hydroxy-2-methylidenebutanoate Chemical compound CC(=O)CC(=O)OC(=O)C(=C)CCO ZGLJYJVYUYQOHR-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- VNGLVZLEUDIDQH-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;2-methyloxirane Chemical compound CC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 VNGLVZLEUDIDQH-UHFFFAOYSA-N 0.000 description 1
- WPSWDCBWMRJJED-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;oxirane Chemical compound C1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 WPSWDCBWMRJJED-UHFFFAOYSA-N 0.000 description 1
- YKXAYLPDMSGWEV-UHFFFAOYSA-N 4-hydroxybutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCO YKXAYLPDMSGWEV-UHFFFAOYSA-N 0.000 description 1
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 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
- 229920002907 Guar gum Polymers 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 241000534018 Larix kaempferi Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- WMTLVUCMBWBYSO-UHFFFAOYSA-N N=C=O.N=C=O.C=1C=CC=CC=1OC1=CC=CC=C1 Chemical compound N=C=O.N=C=O.C=1C=CC=CC=1OC1=CC=CC=C1 WMTLVUCMBWBYSO-UHFFFAOYSA-N 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000196435 Prunus domestica subsp. insititia Species 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- 150000004729 acetoacetic acid derivatives Chemical class 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- IBVAQQYNSHJXBV-UHFFFAOYSA-N adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 239000000305 astragalus gummifer gum Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-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
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- ZEYMDLYHRCTNEE-UHFFFAOYSA-N ethenyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC=C ZEYMDLYHRCTNEE-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 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
- 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
- JESXATFQYMPTNL-UHFFFAOYSA-N mono-hydroxyphenyl-ethylene Natural products OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- MADOXCFISYCULS-UHFFFAOYSA-N octyl 2-sulfanylacetate Chemical compound CCCCCCCCOC(=O)CS MADOXCFISYCULS-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-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
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 208000008842 sick building syndrome Diseases 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010025 steaming Methods 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
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Veneer Processing And Manufacture Of Plywood (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
本発明は接着剤組成物に関し、詳しくは特定の合成エマルジョンにアセトアセチル基を導入することで針葉樹に対し優れた接着性を有し、かつホルムアルデヒドを含まない接着剤組成物に関するものである。 The present invention relates to an adhesive composition, and more particularly to an adhesive composition having excellent adhesiveness to softwood by introducing an acetoacetyl group into a specific synthetic emulsion and not containing formaldehyde.
従来、木材用の耐水性接着剤組成物として、ユリア−ホルムアルデヒド樹脂接着剤、メラミン−ホルムアルデヒド樹脂接着剤、フェノール−ホルムアルデヒド樹脂接着剤、レゾルシノール−ホルムアルデヒド樹脂接着剤等のホルムアルデヒド樹脂系接着剤が知られている。しかし、前記ホルムアルデヒド樹脂系接着剤は、遊離のホルムアルデヒドが残存しているために、該ホルムアルデヒド樹脂系接着剤を用いて接着した建築材製品等からホルムアルデヒドが放出され、これによる健康障害、いわゆるシックハウス症候群の問題がクローズアップされてきた。 Conventionally, formaldehyde resin adhesives such as urea-formaldehyde resin adhesive, melamine-formaldehyde resin adhesive, phenol-formaldehyde resin adhesive, resorcinol-formaldehyde resin adhesive are known as water-resistant adhesive compositions for wood. ing. However, since the formaldehyde resin-based adhesive remains free formaldehyde, formaldehyde is released from the building material product or the like bonded with the formaldehyde resin-based adhesive, resulting in health problems, so-called sick house syndrome. The problem has been close up.
また、前記ホルムアルデヒド樹脂系接着剤のうち、ユリア−ホルムアルデヒド樹脂接着剤、メラミン−ホルムアルデヒド樹脂接着剤、フェノール−ホルムアルデヒド樹脂接着剤の3種の接着剤は、接着の際に加熱圧締する必要があり、厚物材料の接着、特に集成材の接着には適していない。これに対して前記レゾルシノール−ホルムアルデヒド樹脂接着剤は前記加熱圧締は必要としないが、雰囲気温度20℃にて16時間という長時間の冷熱圧締を必要とするために、作業能率が低い。さらに、前記レゾルシノール−ホルムアルデヒド樹脂接着剤は、接着剤自身が赤褐色であり接着層が同色に着色して製品の商品価値を低減するために、用途が限定されるとの問題がある。 Of the formaldehyde resin adhesives, three types of adhesives, urea-formaldehyde resin adhesive, melamine-formaldehyde resin adhesive, and phenol-formaldehyde resin adhesive, need to be heat-pressed during bonding. It is not suitable for the adhesion of thick materials, especially for laminated wood. On the other hand, the resorcinol-formaldehyde resin adhesive does not require the heat pressing, but requires a long-time cold pressing for 16 hours at an atmospheric temperature of 20 ° C., and therefore has a low work efficiency. Further, the resorcinol-formaldehyde resin adhesive has a problem that its use is limited because the adhesive itself is reddish brown and the adhesive layer is colored in the same color to reduce the commercial value of the product.
前記ホルムアルデヒド樹脂系接着剤の問題を解決するために、水溶性高分子水溶液、水性ラテックス、水性エマルジョン等を主剤とし、該主剤に硬化剤としてイソシアネート化合物を配合した水性高分子−イソシアネート系接着剤組成物が知られている。前記水性高分子−イソシアネート系接着剤組成物は、ホルムアルデヒド樹脂を含まないので、遊離のホルムアルデヒドの放出による環境汚染の虞がなく、冷熱圧締が可能であり、接着層が着色することもない。 In order to solve the problems of the formaldehyde resin-based adhesive, an aqueous polymer-isocyanate-based adhesive composition comprising a water-soluble polymer aqueous solution, an aqueous latex, an aqueous emulsion, etc. as a main agent, and an isocyanate compound as a curing agent in the main agent. Things are known. Since the aqueous polymer-isocyanate adhesive composition does not contain a formaldehyde resin, there is no risk of environmental pollution due to the release of free formaldehyde, cold pressing is possible, and the adhesive layer is not colored.
前記水性高分子−イソシアネート系接着剤組成物として、例えば、(A)ポリビニルアルコールの水溶液とエチレン含有量が10〜45重量%であるエチレン−酢酸ビニル共重合体系樹脂エマルジョンの存在化に該共重合体系樹脂エマルジョン中の固形分100重量部当たり、酢酸ビニル及び酢酸ビニル100重量部当たり0〜40重量部の他のビニル重合可能な単量体を合計で100〜600重量部をシード重合してなるエマルジョン、(B)ポリビニルアルコール等の水溶性高分子を含む水溶液、(C)イソシアネート化合物と反応する充填剤、(D)多価イソシアネート化合物からなる水系接着剤(特許文献1)、分子内にアセトアセチル基を有する高分子化合物1重量部に対し、ゴムラテックスおよび/または合成樹脂エマルジョンを固形分として10重量部を上限とする範囲で混合して得られる水溶液または水性エマルジョンであるA液、およびアジピン酸ジヒドラジド等のヒドラジン化合物を含む水溶液または分散液であるB液からなる2液性接着剤(特許文献2)、水溶性高分子水溶液、水性ラテックス、水性エマルジョンの1種または2種以上からなる主剤と、2,4’−ジフェニルメタンジイソシアネート等のイソシアネート化合物からなる硬化剤とを含む接着剤組成物であって、前記硬化剤の全量に対して、ポリメチレンポリフェニルポリイソシアネートを0〜40重量%の範囲で含むことを特徴とする高度耐水性接着剤組成物(特許文献3)等多くの提案がなされている。 Examples of the aqueous polymer-isocyanate-based adhesive composition include (A) an aqueous solution of polyvinyl alcohol and the presence of an ethylene-vinyl acetate copolymer resin emulsion having an ethylene content of 10 to 45% by weight. 100 to 600 parts by weight of a total of 100 to 600 parts by weight of vinyl acetate and 0 to 40 parts by weight of other vinyl polymerizable monomers per 100 parts by weight of solid content in the system resin emulsion Emulsions, (B) aqueous solutions containing water-soluble polymers such as polyvinyl alcohol, (C) fillers that react with isocyanate compounds, (D) aqueous adhesives composed of polyvalent isocyanate compounds (Patent Document 1), Rubber latex and / or synthetic resin emulsion to 1 part by weight of polymer compound having acetyl group A two-part adhesive comprising a liquid A or an aqueous emulsion obtained by mixing within a range of up to 10 parts by weight as a solid content, and a liquid B containing an hydrazine compound such as adipic acid dihydrazide or a dispersion. (Patent Document 2), a water-soluble polymer aqueous solution, an aqueous latex, an adhesive containing a main agent composed of one or more of an aqueous emulsion, and a curing agent composed of an isocyanate compound such as 2,4'-diphenylmethane diisocyanate A highly water-resistant adhesive composition characterized by containing polymethylene polyphenyl polyisocyanate in the range of 0 to 40% by weight with respect to the total amount of the curing agent (Patent Document 3) and many others Proposals have been made.
イソシアネート化合物は、一般に水溶液または水性エマルジョンのように水を含む溶液に直接配合すると、水と激しく反応して、著しく発泡するという性質がある。イソシアネート化合物を疎水性有機溶剤に溶解することにより、該イソシアネート化合物と水との反応を抑制することができ、塗布作業性を改善し、使用可能な時間を延長することができるが、疎水性有機溶剤を使用したために臭気の発生、有機溶剤の揮散に伴う環境汚染の問題が避けられない。 In general, when an isocyanate compound is directly blended into a solution containing water such as an aqueous solution or an aqueous emulsion, it reacts violently with water and foams significantly. By dissolving the isocyanate compound in a hydrophobic organic solvent, the reaction between the isocyanate compound and water can be suppressed, coating workability can be improved, and the usable time can be extended. Due to the use of solvents, odor generation and environmental pollution problems associated with volatilization of organic solvents are inevitable.
水性であっても高接着強度、優れた耐久性、耐水性及び耐熱水性を有ししかも可使時間の長い接着剤組成物として、(A)多糖類を保護コロイドとして、ラジカル重合性不飽和単量体を乳化重合して得られる合成樹脂エマルジョン、(B)ポリビニルアルコールおよび(C)イソシアネート基を有する化合物を含有してなる接着剤組成物が提案(特許文献4参照)されている。 As an adhesive composition that has high adhesive strength, excellent durability, water resistance and hot water resistance even when it is aqueous, and has a long pot life, (A) a polysaccharide as a protective colloid, a radically polymerizable unsaturated monomer An adhesive composition comprising a synthetic resin emulsion obtained by emulsion polymerization of a monomer, (B) polyvinyl alcohol, and (C) a compound having an isocyanate group has been proposed (see Patent Document 4).
これらの、前記各公報記載の接着剤組成物の中には、比重の小さな木材からなる合板の接着には有効であるが、カバ材等のように比重の大きな木材からなる集成材の接着では、集成材に関する日本農林規格の浸せきはく離試験を十分に満足できる耐水性が得られないケース、昨今の高度化した接着剤への要求に対し、耐水性、耐熱性及び耐久性に関して満足せしめられないものも見受けられる。
しかし、近年広葉樹資源が不足し入手難になっており、針葉樹を素材とした合板の比率が年々増加している。針葉樹は特にヤニ成分が多いため、酢酸ビニル樹脂系や水性高分子−イソシアネート系接着剤では針葉樹への密着性、耐水性、耐熱水接着性、耐久性、安定性等の点が極めて不十分なものであり、合板に対し厳しい耐煮沸水性が要求されるJAS特類規格には到底合格しないものであった。
Among these adhesive compositions described in each of the above publications, it is effective for bonding plywood made of wood having a small specific gravity, but in bonding of laminated wood made of wood having a high specific gravity, such as birch material. , Cases where water resistance that can sufficiently satisfy the Japanese Agricultural Standards for wood laminates cannot be obtained, and water resistance, heat resistance and durability cannot be satisfied in response to the recent demand for advanced adhesives Things can also be seen.
However, in recent years, hardwood resources have become scarce and it has become difficult to obtain, and the proportion of plywood made from conifers is increasing year by year. Since softwood has a particularly large amount of spider components, vinyl acetate resin-based and water-based polymer-isocyanate-based adhesives are extremely inadequate in terms of adhesion to softwood, water resistance, hot water adhesion, durability, stability, etc. Therefore, it did not pass JAS special standards that required severe boiling water resistance for plywood.
本発明の目的は、針葉樹等の難接着合板に対し優れた接着性を有し、さらにホルムアルデヒドを放散せず作業性に優れ、とりわけ可使時間が極めて長いという特徴を有する接着剤組成物を提供することにある。 The object of the present invention is to provide an adhesive composition having excellent adhesion to hard-to-adhere plywood such as conifers, excellent workability without releasing formaldehyde, and especially having a very long pot life. There is to do.
本発明は、
[1] (A)保護コロイドに多糖類を使用してラジカル重合性不飽和単量体とアセトアセチル基を有するラジカル重合性不飽和単量体を乳化重合得られたアセトアセチル基を有する合成樹脂エマルジョン(以下単に「アセトアセチル基を有する合成樹脂エマルジョン」という。)、(B)ポリビニルアルコールおよび(C)ビニルエステルエマルジョンからなる樹脂組成物に(D)イソシアネート基を有する化合物を配合したことを特徴とする接着剤組成物、
The present invention
[1] (A) A synthetic resin having an acetoacetyl group obtained by emulsion polymerization of a radically polymerizable unsaturated monomer and a radically polymerizable unsaturated monomer having an acetoacetyl group using a polysaccharide as a protective colloid A resin composition comprising an emulsion (hereinafter simply referred to as “synthetic resin emulsion having an acetoacetyl group”), (B) polyvinyl alcohol and (C) vinyl ester emulsion, and (D) a compound having an isocyanate group is blended. An adhesive composition,
[2] (A)合成樹脂エマルジョンに使用するアセトアセチル基を有するラジカル重合性不飽和単量体は、全ラジカル重合性不飽和単量体100重量部に対して、1〜15重量部の範囲である上記[1]に記載の接着剤組成物、
[3] (A)合成樹脂エマルジョンのゲル分率が、20%以上である上記[1]に記載の接着剤組成物、
[4](A)保護コロイドに多糖類を使用した、ラジカル重合性不飽和単量体およびアセトアセチル基を有するラジカル重合性不飽和単量体を乳化重合で得られたアセトアセチル基を有する合成樹脂エマルジョンの固形分100重量部に対して、(B)ポリビニルアルコールの固形分2〜300重量部の割合で使用した、上記[1]に記載の接着剤組成物、
[5] (A)合成樹脂エマルジョンの固形分100重量部に対して(C)ビニルエステルエマルジョンを固形分として10〜30重量部の割合で配合してなる上記[1]に記載の接着剤組成物、
[6] (D)イソシアネート基を有する化合物が(A)合成樹脂エマルジョンの固形分100重量部に対して2〜200重量部の割合で配合してなる上記[1]に記載の接着剤組成物、
[2] (A) The radical polymerizable unsaturated monomer having an acetoacetyl group used in the synthetic resin emulsion is in the range of 1 to 15 parts by weight with respect to 100 parts by weight of the total radical polymerizable unsaturated monomer. The adhesive composition according to the above [1],
[3] (A) The adhesive composition according to [1], wherein the gel fraction of the synthetic resin emulsion is 20% or more,
[4] (A) Synthesis having radical polymerizable unsaturated monomer and radical polymerizable unsaturated monomer having acetoacetyl group obtained by emulsion polymerization using polysaccharide as protective colloid The adhesive composition according to the above [1], which is used in a proportion of 2 to 300 parts by weight of solid content of (B) polyvinyl alcohol with respect to 100 parts by weight of solid content of the resin emulsion,
[5] The adhesive composition according to the above [1], wherein (A) vinyl ester emulsion is blended in a proportion of 10 to 30 parts by weight as a solid content with respect to 100 parts by weight of a solid content of the synthetic resin emulsion. Stuff,
[6] The adhesive composition according to the above [1], wherein (D) the compound having an isocyanate group is blended at a ratio of 2 to 200 parts by weight with respect to 100 parts by weight of the solid content of the (A) synthetic resin emulsion. ,
[7] 保護コロイドとして多糖類を使用し、ラジカル重合性不飽和単量体とアセトアセチル基を有するラジカル重合性不飽和単量体を乳化重合で得られた合成樹脂エマルジョンにポリビニルアルコールおよびビニルエステル基を有する化合物のエマルジョンを加えて混合して樹脂組成物を得、これにイソシアネート基を有する化合物を配合することからなる接着剤組成物の製造方法、および
[8] 保護コロイドとして多糖類を使用し、ラジカル重合性不飽和単量体とアセトアセチル基を有するラジカル重合性不飽和単量体を乳化重合で得られた合成樹脂エマルジョンにポリビニルアルコールおよびビニルエステル基を有する化合物のエマルジョンを加えて混合して樹脂組成物を得、これにイソシアネート基を有する化合物を配合して製造した接着剤組成物を使用した針葉樹の木質系合板または木質系集成材、を開発することにより上記の課題を解決した。
[7] Using a polysaccharide as a protective colloid, polyvinyl alcohol and vinyl ester are added to a synthetic resin emulsion obtained by emulsion polymerization of a radical polymerizable unsaturated monomer and a radical polymerizable unsaturated monomer having an acetoacetyl group. A method for producing an adhesive composition comprising adding a compound having a group and mixing to obtain a resin composition, and blending the compound having an isocyanate group with the emulsion, and [8] using a polysaccharide as a protective colloid Then, a radically polymerizable unsaturated monomer and a radically polymerizable unsaturated monomer having an acetoacetyl group are mixed with a synthetic resin emulsion obtained by emulsion polymerization by adding an emulsion of polyvinyl alcohol and a compound having a vinyl ester group. To obtain a resin composition, which is blended with a compound having an isocyanate group. Woody plywood or wood-based laminated timber of coniferous using an adhesive composition, have solved the above problems by developing.
本発明によれば、広葉樹のみならず、問題のある針葉樹基材であっても密着性、接着性、耐水性、耐煮沸性が得られ、さらにホルムアルデヒドを放散せず作業性に優れ、可使時間が長いという特徴を有する接着剤組成物が提供できた。 According to the present invention, adhesiveness, adhesiveness, water resistance, boiling resistance can be obtained not only for hardwoods but also problematic softwood base materials, and it has excellent workability without releasing formaldehyde. An adhesive composition having a feature of long time could be provided.
本発明者らは、前記問題点を解決することを目的として鋭意研究を重ねた結果、アセトアセチル基を有するラジカル重合性不飽和単量体を共重合した合成樹脂エマルジョン、ポリビニルアルコールおよびビニルエステルエマルジョンを混合した樹脂組成物に、使用に先立ってイソシアネート基含有化合物を配合して接着剤組成物としたときに始めて前記課題を解決し得ることを見出して本発明を完成した。 As a result of intensive studies aimed at solving the above-mentioned problems, the present inventors have found that a synthetic resin emulsion, a polyvinyl alcohol, and a vinyl ester emulsion obtained by copolymerizing a radical polymerizable unsaturated monomer having an acetoacetyl group The present invention was completed by finding out that the above-mentioned problems could be solved only when an isocyanate group-containing compound was blended into a resin composition mixed with an isocyanate composition prior to use to obtain an adhesive composition.
以下、本発明についてさらに詳細に説明する。
(A)アセトアセチル基を有する合成樹脂エマルジョン
本発明の接着剤組成物に使用する(A)アセトアセチル基を有する合成樹脂エマルジョンは、多糖類を保護コロイドとして用い、アセトアセチル基を有するラジカル重合性不飽和単量体およびこれらと共重合可能な他のラジカル重合性不飽和単量体とを乳化重合することによって得ることができる。
該合成樹脂エマルジョンを調整するにあたって使用される前記多糖類としては、アラビアゴム、ガッティゴム、トラガカントガム、ダムソンゴム、サクラゴム、セイヨウスモモゴム、グアーガムなどが挙げられる。これらの多糖類は、保護コロイドとしての役割を果たすことができる。多糖類を保護コロイドとして用いたときは、(B)ポリビニルアルコールおよび(C)イソシアネート基を有する化合物と組み合わせた接着剤組成物の可使時間を、通常の乳化重合で使用されるアニオン性、カチオン性、両性、および非イオン性界面活性剤や、各種ポリビニルアルコール、ヒドロキシエチルセルロースなどの多糖類以外の水溶性高分子を用いた接着剤組成物に比べて、飛躍的に長くすることが可能となる(特許文献4参照)。
Hereinafter, the present invention will be described in more detail.
(A) Synthetic resin emulsion having an acetoacetyl group (A) The synthetic resin emulsion having an acetoacetyl group used in the adhesive composition of the present invention uses a polysaccharide as a protective colloid and has radical polymerization properties having an acetoacetyl group. It can be obtained by emulsion polymerization of unsaturated monomers and other radical polymerizable unsaturated monomers copolymerizable therewith.
Examples of the polysaccharide used in preparing the synthetic resin emulsion include gum arabic, gutty gum, tragacanth gum, damson gum, cherry gum, peach gum gum, guar gum and the like. These polysaccharides can serve as protective colloids. When a polysaccharide is used as a protective colloid, the usable time of the adhesive composition combined with (B) polyvinyl alcohol and (C) a compound having an isocyanate group is changed to an anionic cation used in ordinary emulsion polymerization. Compared to adhesive compositions using water-soluble polymers other than polysaccharides such as hydrophilic, amphoteric, and nonionic surfactants, various polyvinyl alcohols, and hydroxyethyl cellulose, the length can be dramatically increased. (See Patent Document 4).
(A)ラジカル重合性不飽和単量体とアセトアセチル基を有するラジカル重合性不飽和単量体を乳化重合して合成樹脂エマルジョンを得る際に、保護コロイドとして用いる多糖類の配合量は、全ラジカル重合性不飽和単量体100重量部に対して0.1〜20重量部、好ましくは0.5〜15重量部である。多糖類の配合量が、0.1重量部未満であると、得られた(A)合成樹脂エマルジョンの安定性が悪く、凝集、ゲル化してしまい、20重量部を越えると最終的に得られる接着剤の耐水性が著しく低下するために好ましくない。また、可使時間や接着性能に支障がない範囲で、保護コロイドとして各種ポリビニルアルコール、ヒドロキシエチルセルロースなどを多糖類を併用して用いることも可能である。 (A) When the radical polymerizable unsaturated monomer and the radical polymerizable unsaturated monomer having an acetoacetyl group are emulsion-polymerized to obtain a synthetic resin emulsion, the amount of polysaccharide used as a protective colloid is It is 0.1-20 weight part with respect to 100 weight part of radically polymerizable unsaturated monomers, Preferably it is 0.5-15 weight part. When the blending amount of the polysaccharide is less than 0.1 parts by weight, the obtained (A) synthetic resin emulsion is poorly stable and aggregates and gels, and when it exceeds 20 parts by weight, it is finally obtained. This is not preferable because the water resistance of the adhesive is significantly reduced. In addition, various polyvinyl alcohols, hydroxyethyl cellulose, and the like can be used in combination with polysaccharides as protective colloids within the range that does not hinder the pot life and adhesion performance.
ラジカル重合性不飽和単量体とアセトアセチル基を有するラジカル重合性不飽和単量体を乳化重合して得られる合成樹脂エマルジョンは、アセトアセチル基を含有する単量体、例えばアリルアセトアセテート、ビニルアセトアセテート;2−アセトアセトキシエチルアクリレート、2−アセトアセトキシエチルメタクリレート、2−アセトアセトキシプロピルアクリレート、2−アセトアセトキシプロピルメタクリレート、2−シアノアセトアセトキシエチルメタクリレート等のアルキレングリコールの(メタ)アクリル酸アセト酢酸エステル;2−アセトアセトキシエチルクロトネート、2−アセトアセトキシプロピルクロトネート等のアルキレングリコールのクロトン酸アセト酢酸エステル;N−(アセトアセトキシメチル)アクリルアミド、N−(アセトアセトキシメチル)メタクリルアミド、N−(アセトアセトキシエチル)アクリルアミド、N−(アセトアセトキシエチル)メタクリルアミド等のN−アルキロール(メタ)アクリルアミドのアセト酢酸エステル;2−ヒドロキシエチルアクリレート、2−ヒドロキシエチルメタクリレート、ヒドロキシプロピルアクリレート、2−ヒドロキシ−3−クロロプロピルメタクリレート、1,4−ブチレングリコールモノアクリレート、1,4−ブチレングリコールモノメタクリレート、N−メチロールアクリルアミド、N−メチロールメタクリルアミド、ヒドロキシスチレン等の水酸基を有するエチレン性不飽和単量体等のアセトアセチル化物が例示され、これらは単独又は2種以上が併用される。 A synthetic resin emulsion obtained by emulsion polymerization of a radically polymerizable unsaturated monomer and a radically polymerizable unsaturated monomer having an acetoacetyl group is a monomer containing an acetoacetyl group, such as allyl acetoacetate, vinyl Acetoacetate; (meth) acrylic acid acetoacetate of alkylene glycol such as 2-acetoacetoxyethyl acrylate, 2-acetoacetoxyethyl methacrylate, 2-acetoacetoxypropyl acrylate, 2-acetoacetoxypropyl methacrylate, 2-cyanoacetoacetoxyethyl methacrylate Esters; Crotonic acetoacetate esters of alkylene glycols such as 2-acetoacetoxyethyl crotonate and 2-acetoacetoxypropyl crotonate; N- (acetoacetoxymethyl) acrylic acid Acetoacetate of N-alkylol (meth) acrylamide such as N- (acetoacetoxymethyl) methacrylamide, N- (acetoacetoxyethyl) acrylamide, N- (acetoacetoxyethyl) methacrylamide; 2-hydroxyethyl acrylate 2-hydroxyethyl methacrylate, hydroxypropyl acrylate, 2-hydroxy-3-chloropropyl methacrylate, 1,4-butylene glycol monoacrylate, 1,4-butylene glycol monomethacrylate, N-methylol acrylamide, N-methylol methacrylamide, Examples include acetoacetylated products such as ethylenically unsaturated monomers having a hydroxyl group such as hydroxystyrene, and these may be used alone or in combination of two or more.
また、アセトアセチル基を有するラジカル重合性不飽和単量体と共重合可能な他のラジカル重合性不飽和単量体としては、特に限定されるものではないが、(メタ)アクリル酸メチル、(メタ)アクリル酸エチル、(メタ)アクリル酸n−プロピル、(メタ)アクリル酸イソプロピル、(メタ)アクリル酸n−ブチル、(メタ)アクリル酸イソブチル、(メタ)アクリル酸sec−ブチル、(メタ)アクリル酸t−ブチル、(メタ)アクリル酸n−ペンチル、(メタ)アクリル酸2−エチルヘキシル、(メタ)アクリル酸n−オクチル、(メタ)アクリル酸ラウリル、(メタ)アクリル酸ステアリル、(メタ)アクリル酸シクロヘキシル、(メタ)アクリル酸2−メトキシエチル、(メタ)アクリル酸2−エトキシエチル、(メタ)アクリル酸2−メトキシプロピル、(メタ)アクリル酸3−メトキシプロピル、(メタ)アクリル酸2−メトキシブチル、(メタ)アクリル酸3−メトキシブチル、(メタ)アクリル酸4−メトキシブチル、(メタ)アクリル酸ヒドロキシエチル、(メタ)アクリル酸ヒドロキシプロピル、(メタ)アクリル酸ヒドロキシブチルなどの(メタ)アクリル酸エステル類、およびこれと共重合可能な単量体、たとえばアクリル酸、メタクリル酸、クロトン酸、イタコン酸などのα、β−エチレン性不飽和カルボン酸類、スチレン、ビニルスチレンなどの芳香族ビニル化合物、などが挙げられる。なお該共重合体中のアセトアセチル基を含有する単量体の含有量は全ラジカル重合性不飽和単量体100重量部に対して1〜15重量部、好ましくは2〜10重量部配合する。 Further, the other radical polymerizable unsaturated monomer copolymerizable with the radical polymerizable unsaturated monomer having an acetoacetyl group is not particularly limited, but methyl (meth) acrylate, ( (Meth) ethyl acrylate, (meth) acrylic acid n-propyl, (meth) acrylic acid isopropyl, (meth) acrylic acid n-butyl, (meth) acrylic acid isobutyl, (meth) acrylic acid sec-butyl, (meth) T-butyl acrylate, n-pentyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, (meth) Cyclohexyl acrylate, 2-methoxyethyl (meth) acrylate, 2-ethoxyethyl (meth) acrylate, (meth) acrylic 2-methoxypropyl, (meth) acrylic acid 3-methoxypropyl, (meth) acrylic acid 2-methoxybutyl, (meth) acrylic acid 3-methoxybutyl, (meth) acrylic acid 4-methoxybutyl, (meth) acrylic acid (Meth) acrylic esters such as hydroxyethyl, hydroxypropyl (meth) acrylate, hydroxybutyl (meth) acrylate, and monomers copolymerizable therewith, such as acrylic acid, methacrylic acid, crotonic acid, itacone Examples include α, β-ethylenically unsaturated carboxylic acids such as acids, aromatic vinyl compounds such as styrene and vinyl styrene, and the like. The content of the monomer containing an acetoacetyl group in the copolymer is 1 to 15 parts by weight, preferably 2 to 10 parts by weight, based on 100 parts by weight of all radical polymerizable unsaturated monomers. .
さらに、本発明における(A)アセトアセチル基を有する合成樹脂エマルジョンのゲル分率は、20%以上となるように調製する。ゲル分率が20%より小さいと、最終的に得られた接着剤の接着強度は小さく、耐水性は著しく低下してしまい、好ましくない。
ここで、合成樹脂エマルジョンのゲル分率は次の様にして測定したものである。
Further, the gel fraction of the synthetic resin emulsion (A) having an acetoacetyl group in the present invention is prepared to be 20% or more. When the gel fraction is less than 20%, the adhesive strength of the finally obtained adhesive is small, and the water resistance is remarkably lowered, which is not preferable.
Here, the gel fraction of the synthetic resin emulsion was measured as follows.
合成樹脂エマルジョンをガラス板上に流延して、20℃、湿度65%の下で6日間乾燥し、厚さ約0.3mmのフィルムを作成する。この乾燥フィルムを精秤(この時の重量をW1とする)した。次いでこれを金網で包み、20℃のテトラヒドロフラン(フィルム0.5gに対しTHF50mlの割合)中に24時間浸漬してから引き上げて、風乾しフィルムの重量を精秤する(この時の重量をW2とする)。
ゲル分率は下式で算出した。
(W2/W1)×100 =ゲル分率(%)
The synthetic resin emulsion is cast on a glass plate and dried at 20 ° C. and a humidity of 65% for 6 days to form a film having a thickness of about 0.3 mm. The dry film was precisely weighed (the weight at this time is W1). This is then wrapped in a wire mesh, immersed in tetrahydrofuran at 20 ° C. (ratio of 50 ml of THF to 0.5 g of the film) for 24 hours, pulled up, air-dried, and the weight of the film is precisely weighed (the weight at this time is W 2 And).
The gel fraction was calculated by the following formula.
(W 2 / W 1 ) × 100 = Gel fraction (%)
本発明の接着剤において、(A)アセトアセチル基を有する合成樹脂エマルジョンは通常の乳化重合法に従って製造することができる。重合に際しては、通常一般に用いられている重合開始剤が使用される。具体例としては、過酸化水素、過硫酸カリウム、過硫酸アンモニウム等の水溶性無機過酸化物または過硫酸塩、クメンハイドロパーオキサイド、ベンゾイルパーオキサイドなどの有機過酸化物、アゾビスイソブチルニトリルなどのアゾ化合物が挙げられる。また、前記重合開始剤は、酒石酸、蟻酸、シュウ酸、酸性亜硫酸ソーダ、ロンガリットなどの還元剤と併用することも通常行われる。重合開始剤の使用量は、全ラジカル重合性不飽和単量体100重量部に対して0.1〜2.0重量部が好ましい。またラジカル重合性不飽和単量体は、これを一括もしくは分割して、あるいは連続的に滴下して反応に供することができる。重合温度は、通常の60〜90℃で行うことができる。 In the adhesive of the present invention, (A) a synthetic resin emulsion having an acetoacetyl group can be produced according to a usual emulsion polymerization method. In the polymerization, a generally used polymerization initiator is used. Specific examples include water-soluble inorganic peroxides or persulfates such as hydrogen peroxide, potassium persulfate, and ammonium persulfate, organic peroxides such as cumene hydroperoxide and benzoyl peroxide, and azo such as azobisisobutylnitrile. Compounds. Further, the polymerization initiator is usually used in combination with a reducing agent such as tartaric acid, formic acid, oxalic acid, acidic sodium sulfite, or longalite. As for the usage-amount of a polymerization initiator, 0.1-2.0 weight part is preferable with respect to 100 weight part of all radically polymerizable unsaturated monomers. Further, the radically polymerizable unsaturated monomer can be subjected to the reaction by batch or divided or continuously dropped. The polymerization temperature can be carried out at a normal temperature of 60 to 90 ° C.
また一般に乳化重合に際して用いられる分子量調整剤として、ラウリルメルカプタン、オクチルメルカプタン、2−メルカプトエチルアルコール、2−メルカプトプロピオン酸、チオグリコール酸オクチル等の連鎖移動剤を用いることが出来る。また、合成樹脂エマルジョンで多用される造膜助剤その他の添加剤も必要に応じて添加することができる。 In addition, chain transfer agents such as lauryl mercaptan, octyl mercaptan, 2-mercaptoethyl alcohol, 2-mercaptopropionic acid, and octyl thioglycolate can be used as molecular weight regulators generally used in emulsion polymerization. Moreover, the film-forming aid and other additives frequently used in the synthetic resin emulsion can be added as necessary.
(B)ポリビニルアルコール
本発明の接着剤組成物に使用する(B)ポリビニルアルコールは、通常の完全ケン化物または部分ケン化物のいずれも使用することができ、またメルカプト基変性品、アセトアセチル基変性品のような変性ポリビニルアルコールも同様に使用することができる。
(B) Polyvinyl alcohol (B) Polyvinyl alcohol used in the adhesive composition of the present invention can be either a normal fully saponified product or a partially saponified product, and a mercapto group-modified product or an acetoacetyl group-modified product. Modified polyvinyl alcohol such as products can be used as well.
接着剤組成物
本発明の接着剤組成物において、(A)合成樹脂エマルジョンと(B)ポリビニルアルコールの混合物をもって主剤とし、その配合は、前記(A)合成樹脂エマルジョンの固形分100重量部に対して、(B)ポリビニルアルコールの固形分が2〜300重量部、より好ましくは5〜200重量部の範囲となるように配合するのがよい。(B)ポリビニルアルコールが2重量部未満では、以下に説明する(D)イソシアネート基を有する化合物を添加した後の、最終的に得られた接着剤組成物の粘度上昇が大きくなるため好ましくない。また、(B)ポリビニルアルコールが300重量部を超えると最終的に得られた接着剤組成物の耐水性が低下するため好ましくない。
Adhesive composition In the adhesive composition of the present invention, a mixture of (A) a synthetic resin emulsion and (B) polyvinyl alcohol is used as a main agent, and the blending is based on 100 parts by weight of the solid content of the (A) synthetic resin emulsion. (B) The solid content of the polyvinyl alcohol is preferably 2 to 300 parts by weight, more preferably 5 to 200 parts by weight. When (B) the polyvinyl alcohol is less than 2 parts by weight, the viscosity increase of the finally obtained adhesive composition after addition of the compound (D) having an isocyanate group, which will be described below, is not preferable. Moreover, when (B) polyvinyl alcohol exceeds 300 weight part, since the water resistance of the adhesive composition finally obtained falls, it is unpreferable.
(C)ビニルエステルエマルジョン
本発明に使用するビニルエステルは、エポキシ樹脂とα、β−不飽和一塩基酸との反応により得ることができる。エポキシ樹脂は、大別してビスフェノール構造を有するいわゆる「エピ−ビス型」と、ノボラック構造を有する「ノボラックエポキシ型」があり、これ以外にも鬼も環状脂肪族構造を有する「グリシジルエーテル型」、ポリエーテルポリオールの「グリシジルエーテル型」、多価アルコールの「グリシジルエーテル型」、等を挙げることが出来るが、何れも本発明に使用可能である。但し、コスト、物性上から「エピ−ビス型」のエポキシ樹脂が有利である。
(C) Vinyl ester emulsion The vinyl ester used in the present invention can be obtained by the reaction of an epoxy resin and an α, β-unsaturated monobasic acid. Epoxy resins are broadly classified into so-called “epi-bis type” having a bisphenol structure and “novolac epoxy type” having a novolac structure. In addition, the demon has a “glycidyl ether type” having a cyclic aliphatic structure, poly Examples thereof include “glycidyl ether type” of ether polyol and “glycidyl ether type” of polyhydric alcohol, and any of them can be used in the present invention. However, from the viewpoint of cost and physical properties, an “epi-bis type” epoxy resin is advantageous.
エポキシ樹脂と反応させてビニルエステルとするためのα、β−不飽和一塩基酸としては、アクリル酸、メタクリル酸(以下両者を一括して「(メタ)アクリル酸」という。)クロトン酸、マレイン酸モノエステル類、フマル酸モノエステル類、イタコン酸モノエステル類などが挙げられ、要求される樹脂の硬化性の遅速により必要に応じて選択される。一般には(メタ)アクリル酸が使用される。
エポキシ樹脂とα、β−不飽和一塩基酸との反応は、通常空気(酸素)気流下で、3級アミン類、4級アンモニウム類、第4級アンモニウム塩類、トリフェニルフォスフィンなどの触媒の存在下、100〜140℃に加熱して行われる。必要に応じて反応性希釈剤、例えば多価アルコール〜(メタ)アクリレートの共存下で反応を行うこともできる。本発明に使用できる反応性希釈剤の種類並びに使用量には特に制限する必要はないが、耐熱水性を要求される木材接着などに使用する場合にはビニルエステルと反応性希釈剤、例えば多価アルコール〜(メタ)アクリレートの合計量に対し、ビニルエステルの配合量は少なくとも10重量%が必要であり、50重量%以上を配合することが好ましい。
Examples of α, β-unsaturated monobasic acids to be reacted with epoxy resins to form vinyl esters include acrylic acid, methacrylic acid (hereinafter collectively referred to as “(meth) acrylic acid”), crotonic acid, and maleic acid. Examples thereof include acid monoesters, fumaric acid monoesters, itaconic acid monoesters, and the like, which are selected according to the required slowness of curability of the resin. In general, (meth) acrylic acid is used.
The reaction between the epoxy resin and the α, β-unsaturated monobasic acid is usually carried out under a flow of air (oxygen) by a catalyst such as a tertiary amine, a quaternary ammonium, a quaternary ammonium salt, or triphenylphosphine. It is carried out by heating to 100 to 140 ° C. in the presence. If necessary, the reaction can be carried out in the presence of a reactive diluent such as a polyhydric alcohol to (meth) acrylate. The type and amount of the reactive diluent that can be used in the present invention need not be particularly limited. However, when used for wood bonding or the like that requires hot water resistance, a vinyl ester and a reactive diluent such as polyvalent The compounding amount of the vinyl ester is required to be at least 10% by weight with respect to the total amount of alcohol to (meth) acrylate, and preferably 50% by weight or more.
この多価アルコール〜(メタ)アクリレートは、多価アルコールを(メタ)アクリル酸でエステル化することにより得られる。多価アルコールとしては例えばエチレングリコール、ネオペンチルグリコール、1,4−シクロヘキサンジメタノール、ビスフェノールAエチレンオキシド付加物、ビスフェノールAプロピレンオキシド付加物、ポリエチレングリコール、ポリプロピレングリコール、トリメチロールプロパン、グリセリン、ペンタエリスリットなどが挙げられる。 This polyhydric alcohol to (meth) acrylate can be obtained by esterifying polyhydric alcohol with (meth) acrylic acid. Examples of the polyhydric alcohol include ethylene glycol, neopentyl glycol, 1,4-cyclohexanedimethanol, bisphenol A ethylene oxide adduct, bisphenol A propylene oxide adduct, polyethylene glycol, polypropylene glycol, trimethylolpropane, glycerin, pentaerythritol, etc. Is mentioned.
ビニルエステルエマルジョンの配合量は前記(A)合成樹脂エマルジョンの固形分100重量部に対して固形分10〜30重量部、好ましくは15〜25重量部の割合である。ビニルエステルエマルジョンの配合量が10重量部以下の場合は架橋密度が低下し針葉樹基材での耐煮沸性が低下するため好ましくない。
また、ビニルエステルエマルジョンの配合量が30重量部以上の場合は、樹脂配合後のポットライフが短くなるため好ましくない。
The compounding amount of the vinyl ester emulsion is a ratio of 10 to 30 parts by weight, preferably 15 to 25 parts by weight, based on 100 parts by weight of the solid content of the (A) synthetic resin emulsion. When the blending amount of the vinyl ester emulsion is 10 parts by weight or less, the crosslinking density is lowered, and the boiling resistance in the softwood base material is lowered, which is not preferable.
Moreover, when the compounding quantity of a vinyl ester emulsion is 30 weight part or more, since the pot life after resin compounding becomes short, it is unpreferable.
(D)イソシアネート基を有する化合物
本発明の接着剤組成物に使用する(D)イソシアネート基を含有する化合物は、1分子中に2個以上のイソシアネート基を有しているものであれば特に制限はなく、例としては、ヘキサメチレンジイソシアネートのような脂肪族イソシアネート、m−およびp−フェニレンジイソシアネート、トリレン−2,4−および−2,6−ジイソシアネート、ジフェニルメタン−4,4’−ジイソシアネート、ジフェニレン−4,4’−ジイソシアネート、4,4’−ジイソシアネート−3,3’−ジメチルジフェニル、3−メチル−ジフェニルメタン−4,4’−ジイソシアネート、ジフェニルエーテルジイソシアネートのような芳香族イソシアネート、およびシクロヘキサン−2,4−および−2,3−ジイソシアネート、イソホロンジイソシアネートのような脂環族イソシアネートなどが挙げられる。これらは単独または2種以上混合して使用することができる。また過剰のジイソシアネートまたは多官能ポリイソシアネートとヒドロキシル末端ポリエステルまたはヒドロキシル末端ポリエーテルとの反応により生成されたイソシアネート末端プレポリマー、並びに過剰のジイソシアネートまたは多官能ポリイソシアネートとエチレングリコール、トリメチロールプロパンまたは1,3−ブタンジオールのような単量体ポリオールまたはその混合物との反応により得られる生成物も使用可能である。
(D) Compound having isocyanate group The compound containing (D) isocyanate group used in the adhesive composition of the present invention is particularly limited as long as it has two or more isocyanate groups in one molecule. Examples include aliphatic isocyanates such as hexamethylene diisocyanate, m- and p-phenylene diisocyanate, tolylene-2,4- and -2,6-diisocyanate, diphenylmethane-4,4'-diisocyanate, diphenylene- Aromatic isocyanates such as 4,4′-diisocyanate, 4,4′-diisocyanate-3,3′-dimethyldiphenyl, 3-methyl-diphenylmethane-4,4′-diisocyanate, diphenyl ether diisocyanate, and cyclohexane-2,4 -And -2,3-diisocyanate Sulfonates, such as alicyclic isocyanates such as isophorone diisocyanate. These can be used alone or in admixture of two or more. Also, isocyanate-terminated prepolymers formed by reaction of excess diisocyanate or polyfunctional polyisocyanate with hydroxyl-terminated polyester or hydroxyl-terminated polyether, and excess diisocyanate or polyfunctional polyisocyanate with ethylene glycol, trimethylolpropane or 1,3 Products obtained by reaction with monomeric polyols such as butanediol or mixtures thereof can also be used.
(D)イソシアネート基を含有する化合物の配合量は、使用する目的により任意に決定すればよいが、好ましくは(A)合成樹脂エマルジョンと(B)ポリビニルアルコールの組成物(樹脂組成物から(C)成分を除いたもの)の固形分100重量部に対し、固形分で2〜100重量部、好ましくは5〜70重量部の範囲となるように配合するのがよい。(D)イソシアネート基を含有する化合物の配合量が2重量部未満では十分な接着力が得られなくなるため好ましくない。また、(D)イソシアネート基を含有する化合物の配合量が100重量部を超えると配合後の可使時間が短くなり、かつ粘度上昇が大きくなるため好ましくない。 (D) The compounding quantity of the compound containing an isocyanate group may be arbitrarily determined depending on the purpose of use, but preferably (A) a composition of synthetic resin emulsion and (B) polyvinyl alcohol (from the resin composition (C It is preferable to add 2 to 100 parts by weight, preferably 5 to 70 parts by weight with respect to 100 parts by weight of the solid content of the component (excluding the component)). (D) If the compounding quantity of the compound containing an isocyanate group is less than 2 parts by weight, a sufficient adhesive force cannot be obtained, which is not preferable. Moreover, when the compounding quantity of the compound containing (D) isocyanate group exceeds 100 weight part, since the pot life after mixing | blending becomes short and a viscosity raise becomes large, it is unpreferable.
さらに、本発明の接着剤には、必要に応じて炭酸カルシウム、クレー、カオリン、タルク、木粉などの充填剤、小麦粉などの増量剤、酸化チタン等の顔料あるいはその他、防腐剤、防錆剤などの各種添加剤を適宜添加することができる。
また、本発明の接着剤を使用する場合の塗布方法あるいは接着方法などについては、特に制約はなく、従来行われてきたようなものであれば、いかなる方法によっても行うことができる。例えば、木材などの接着面に接着剤組成物を刷毛塗り等で塗布し、接着面を貼り合わせて圧力を加えて固定する圧締法などに使用することができる。また、本発明の接着剤組成物の乾燥方法は加熱圧締法、常温圧締法のいずれの方法でも十分な接着強度を得ることができる。
Furthermore, the adhesive of the present invention includes, as necessary, fillers such as calcium carbonate, clay, kaolin, talc, and wood flour, fillers such as wheat flour, pigments such as titanium oxide, and others, antiseptics, rust inhibitors Various additives such as can be appropriately added.
Moreover, there is no restriction | limiting in particular about the application | coating method in the case of using the adhesive agent of this invention, or an adhesion | attachment method, It can carry out by what kind of method, if it has been performed conventionally. For example, it can be used in a pressing method in which an adhesive composition is applied to an adhesive surface of wood or the like by brush coating, and the adhesive surface is bonded and fixed by applying pressure. In addition, the adhesive composition of the present invention can be dried by any of the heat pressing method and the room temperature pressing method to obtain sufficient adhesive strength.
本発明の接着剤組成物は、優れた耐久性、耐水性および耐熱水接着力を提供することができ、イソシアネート基を有する化合物を添加した後も粘度の上昇が少なく、発泡もほとんどなく、且つ可使時間を著しく長くして作業性を改善したものである。すなわち、本発明の接着剤組成物は、既に記述したようにきわめて大きな利点と特長を有しているので、広範な用途が期待できる。特に可使時間が長いこと、加熱硬化にとどまらず常温硬化が可能なこと、優れた強度や作業性、ホルムアルデヒドを含有しないこと、最大の特徴はヤニ分の多い針葉樹等の接着にも使用可能であることなどから、特に針葉樹の合板、化粧合板さらには繊維ボード、繊維製品、紙製品など、幅広い用途の接着剤として有用である。 The adhesive composition of the present invention can provide excellent durability, water resistance and hot water adhesion, little increase in viscosity after addition of a compound having an isocyanate group, almost no foaming, and Workability has been improved by significantly extending the pot life. That is, since the adhesive composition of the present invention has extremely great advantages and features as described above, a wide range of uses can be expected. In particular, it has a long pot life, can be cured at room temperature as well as heat-cured, has excellent strength and workability, does not contain formaldehyde, and has the greatest features that can be used for bonding softwood and other softwood. For this reason, it is particularly useful as an adhesive for a wide range of applications such as softwood plywood, decorative plywood, fiberboard, fiber products, and paper products.
以下、本発明を実施例および比較例により更に具体的に説明するが、本発明は決してこれら例示例にのみ限定されるものではない。なお、実施例および比較例中、「部」および「%」は特に断りのない限り、重量基準を示すものとする。 EXAMPLES Hereinafter, although an Example and a comparative example demonstrate this invention further more concretely, this invention is not limited only to these illustration examples at all. In the examples and comparative examples, “parts” and “%” are based on weight unless otherwise specified.
(A)合成樹脂エマルジョンの合成
(製造例1)
攪拌機、温度計、還流冷却器、滴下ロートを備えた1リットルセパラブルフラスコに、アラビアゴムの20%水溶液300部とイオン交換水210部を仕込み、窒素ガスを送入しつつ、反応容器内を80℃に昇温した。その後、、メタアクリル酸メチル225部とアクリル酸ブチル225部、2ヒドロキシエチルアクリレート22.5部、アセトアセトキシエチルメタクリレート14.5部との単量体混合液を4時間かけて滴下した。また、過硫酸アンモニウム2部にイオン交換水を加え、全量を50gとした水溶液を、前記単量体混合液と同時に滴下し、乳化重合を行った。
(A) Synthesis of synthetic resin emulsion (Production Example 1)
A 1-liter separable flask equipped with a stirrer, thermometer, reflux condenser, and dropping funnel was charged with 300 parts of a 20% aqueous solution of gum arabic and 210 parts of ion-exchanged water. The temperature was raised to 80 ° C. Thereafter, a monomer mixture of 225 parts of methyl methacrylate, 225 parts of butyl acrylate, 22.5 parts of 2hydroxyethyl acrylate, and 14.5 parts of acetoacetoxyethyl methacrylate was added dropwise over 4 hours. Further, ion exchange water was added to 2 parts of ammonium persulfate, and an aqueous solution with a total amount of 50 g was added dropwise at the same time as the monomer mixture to perform emulsion polymerization.
なお、このときフラスコの内温が80〜85℃になるよう外温をコントロールした。滴下終了後、80〜85℃で1時間保持した後、30℃以下に冷却しエマルジョンを得た。得られた水性エマルジョンの不揮発分(105℃−1時間乾燥)は48.5%、粘度(BH型粘度計、No.ローター、10rpm、23℃)は7,000mPa・s、ゲル分率は35%であった。この配合比を表1に示す。
(製造例2−4)
製造例1と同様にして、表1に示す配合比でエマルジョンを作製した。
At this time, the external temperature was controlled so that the internal temperature of the flask was 80 to 85 ° C. After completion of dropping, the mixture was held at 80 to 85 ° C. for 1 hour, and then cooled to 30 ° C. or lower to obtain an emulsion. The resulting aqueous emulsion had a non-volatile content (dried at 105 ° C. for 1 hour) of 48.5%, a viscosity (BH viscometer, No. rotor, 10 rpm, 23 ° C.) of 7,000 mPa · s, and a gel fraction of 35. %Met. This blending ratio is shown in Table 1.
(Production Example 2-4)
In the same manner as in Production Example 1, emulsions were produced with the blending ratios shown in Table 1.
(実施例1)
製造例1で得られた合成樹脂エマルジョンの固形分100部に対し、ポリビニルアルコールPVA117(クラレ製、完全ケン化)の15%水溶液を固形分が50部、炭酸カルシウム240重量部、60%ビニルエステルエマルジョンを固形分で15重量部を加えて混合したものを主剤とした。主剤100部中の合成樹脂エマルジョンの固形分に対しイソシアネートを含有する化合物、ミリオネートMR−100(日本ポリウレタン製、ポリメチレンポリフェニルイソシアネート)を30部添加し、十分混合して実施例1の接着剤組成物として性能評価を行った。配合比は表2に示す。
(Example 1)
50 parts of a 15% aqueous solution of polyvinyl alcohol PVA117 (manufactured by Kuraray, completely saponified), 50 parts by weight of calcium carbonate, 240 parts by weight of calcium carbonate, 60% vinyl ester with respect to 100 parts of the solid content of the synthetic resin emulsion obtained in Production Example 1 The emulsion was mixed with 15 parts by weight of solid as a main component. 30 parts of an isocyanate-containing compound, Millionate MR-100 (manufactured by Nippon Polyurethane, polymethylene polyphenyl isocyanate) is added to the solid content of the synthetic resin emulsion in 100 parts of the main agent, and the mixture is mixed thoroughly to give the adhesive of Example 1 Performance evaluation was performed as a composition. The blending ratio is shown in Table 2.
(実施例2,比較例1−5)
実施例1と同様にして、表2に示す割合で各種の接着剤組成物を作製した。
(合板による接着試験)
(Example 2, Comparative Example 1-5)
In the same manner as in Example 1, various adhesive compositions were produced at the ratios shown in Table 2.
(Adhesion test with plywood)
実施例1、2および比較例1〜5で得られた接着剤組成物を用いて針葉樹単板を接着し、合板の引張り剪断強度を測定した。測定方法と測定条件を以下に記す。また、測定結果を表3に示す。 Softwood veneers were bonded using the adhesive compositions obtained in Examples 1 and 2 and Comparative Examples 1 to 5, and the tensile shear strength of the plywood was measured. The measurement method and measurement conditions are described below. The measurement results are shown in Table 3.
(1)接着条件
基材;カラ松単板(厚さ0.55/1.2/0.55mm クロス貼り3ply)、含水率8%
塗布量;220g/m2(片面塗布)
圧締;冷圧 10kg/cm2−30分 → 熱圧 120℃×10kg/cm2−2分
(1) Adhesion conditions Base material: Karamatsu single plate (thickness 0.55 / 1.2 / 0.55mm, cross-bonded 3ply), moisture content 8%
Application amount: 220 g / m 2 (single-sided application)
Clamping: Cold pressure 10 kg / cm 2 -30 minutes → Hot pressure 120 ° C x 10 kg / cm 2 -2 minutes
(2)試験方法
JASによる引張りせん断試験
(3)測定方法
常態接着強度;20℃、65%RH下の標準状態で測定
スチーミング処理試験(JAS特類);室温の水中で2時間以上浸漬した後、120℃で3時間スチーミングし冷めるまで室温の水中に浸漬後、濡れたままの状態で測定
また、配合4時間経過後の粘度上昇率も合わせて測定した。
(2) Test method Tensile shear test by JAS (3) Measurement method Normal state adhesive strength; measured under standard conditions at 20 ° C. and 65% RH Steaming test (JAS special); immersed in water at room temperature for 2 hours or more Thereafter, it was steamed at 120 ° C. for 3 hours and immersed in water at room temperature until cooled, and measured in a wet state. The viscosity increase rate after 4 hours of blending was also measured.
本発明は、合成エマルジョンにアセトアセチル基を導入することで、広葉樹のみならず樹脂が多くて接着性に問題のある針葉樹基材であっても、密着性、接着性、耐水性、耐煮沸性のある接着剤組成物とすることが出来た。本接着剤組成物は水性エマルジョンであって、原則的に有機溶剤を含まないため、臭気及び環境汚染が少なく、全くホルムアルデヒドを放散せず、作業性に優れ、可使時間が長いという特徴を有する接着剤組成物が提供できた。 The present invention introduces an acetoacetyl group into a synthetic emulsion, so that the adhesiveness, adhesiveness, water resistance, boiling resistance can be obtained not only for hardwoods but also for softwood base materials that have many resins and have problems with adhesion. It was able to be set as the adhesive composition with. Since this adhesive composition is an aqueous emulsion and does not contain organic solvents in principle, it has the characteristics of low odor and environmental pollution, no formaldehyde emission, excellent workability, and long usable time. An adhesive composition could be provided.
Claims (8)
Synthetic resin emulsion obtained by emulsion polymerization of radical polymerizable unsaturated monomer and radical polymerizable unsaturated monomer having acetoacetyl group using polysaccharide as protective colloid has polyvinyl alcohol and vinyl ester groups A coniferous wood-based plywood or wood-based laminated lumber using an adhesive composition produced by adding and mixing a compound emulsion to obtain a resin composition and blending this with a compound having an isocyanate group.
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Cited By (3)
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JP2009203368A (en) * | 2008-02-28 | 2009-09-10 | Showa Highpolymer Co Ltd | Adhesive composition for wood |
CN103360994A (en) * | 2012-03-26 | 2013-10-23 | 吴祖顺 | Biomass aldehyde-free adhesive for plywood |
JP2015174320A (en) * | 2014-03-14 | 2015-10-05 | 株式会社オーシカ | Manufacturing method of woody composite material, and aqueous adhesive composition used for the same |
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JP2009203368A (en) * | 2008-02-28 | 2009-09-10 | Showa Highpolymer Co Ltd | Adhesive composition for wood |
CN103360994A (en) * | 2012-03-26 | 2013-10-23 | 吴祖顺 | Biomass aldehyde-free adhesive for plywood |
JP2015174320A (en) * | 2014-03-14 | 2015-10-05 | 株式会社オーシカ | Manufacturing method of woody composite material, and aqueous adhesive composition used for the same |
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