JP2006015613A - Laminated plywood - Google Patents
Laminated plywood Download PDFInfo
- Publication number
- JP2006015613A JP2006015613A JP2004195920A JP2004195920A JP2006015613A JP 2006015613 A JP2006015613 A JP 2006015613A JP 2004195920 A JP2004195920 A JP 2004195920A JP 2004195920 A JP2004195920 A JP 2004195920A JP 2006015613 A JP2006015613 A JP 2006015613A
- Authority
- JP
- Japan
- Prior art keywords
- plywood
- resin
- laminated
- glass transition
- transition temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011120 plywood Substances 0.000 title claims abstract description 52
- 229920005989 resin Polymers 0.000 claims abstract description 46
- 239000011347 resin Substances 0.000 claims abstract description 46
- 239000000126 substance Substances 0.000 claims abstract description 35
- 239000000839 emulsion Substances 0.000 claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 25
- 230000009477 glass transition Effects 0.000 claims abstract description 23
- 239000000203 mixture Substances 0.000 claims abstract description 23
- 239000000178 monomer Substances 0.000 claims description 33
- 239000007787 solid Substances 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
- 238000001035 drying Methods 0.000 abstract description 6
- 150000001875 compounds Chemical class 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 2
- 239000004568 cement Substances 0.000 description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000005336 cracking Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 239000011398 Portland cement Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- -1 pH adjusters Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000945 filler Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000010440 gypsum Substances 0.000 description 4
- 229910052602 gypsum Inorganic materials 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000011505 plaster Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000001023 inorganic pigment Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 150000004760 silicates Chemical class 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011400 blast furnace cement Substances 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000011083 cement mortar Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 150000002826 nitrites Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000011433 polymer cement mortar Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003829 resin cement Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- XDRLAGOBLZATBG-UHFFFAOYSA-N 1-phenylpenta-1,4-dien-3-one Chemical compound C=CC(=O)C=CC1=CC=CC=C1 XDRLAGOBLZATBG-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 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
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000047703 Nonion Species 0.000 description 1
- 241000238633 Odonata Species 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QROGIFZRVHSFLM-QHHAFSJGSA-N [(e)-prop-1-enyl]benzene Chemical compound C\C=C\C1=CC=CC=C1 QROGIFZRVHSFLM-QHHAFSJGSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 1
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 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
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012948 isocyanate Substances 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
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000013053 water resistant agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Finished Plywoods (AREA)
- Laminated Bodies (AREA)
Abstract
Description
本発明は合板表面に例えばセメント系セルフレベリング(以下SLと略)材、石膏系SL材等を塗布・乾燥させた時に、セメント硬化物または石膏硬化物の耐ワレ、密着性が良好な合板に関するものである。さらに詳しくは合板表面に水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)とガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)とからなる配合物を、積層された合板に関する。 The present invention relates to a plywood having good crack resistance and adhesion of a hardened cement or a gypsum hardened material when, for example, a cement-based self-leveling (hereinafter abbreviated as SL) material or a gypsum-based SL material is applied to the plywood surface and dried. Is. More specifically, a composition comprising one or more curable substances (1) selected from a hydraulic substance and a pneumatic substance on the plywood surface and a resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or lower, It relates to laminated plywood.
合板表面に各種SL材を塗布・乾燥させたものは、建築部材の床、壁などに使われている。従来、合板と各種SL材耐ワレ性及びSL材との密着性性を向上させるために、樹脂エマルジョン等を塗布することがあった。
しかしながら、近年床、壁の使用条件の多様化によるSL材のワレの発生が起き易くなっている。また合板からのホルムアルデヒド放散を防止するために合板作製時にパラフィン等の成分を配合する等の処理を施していることがあり、パラフィンの表面への移行等が問題となる場合がある。その結果、従来の樹脂エマルジョンと合板の間に一層増えることになり、結果として合板とSL材の密着性が不良となることが起きている。
The various plywood surfaces coated with various SL materials and dried are used on the floors and walls of building materials. Conventionally, a resin emulsion or the like is sometimes applied in order to improve the adhesion between the plywood and various SL materials and the SL material.
However, in recent years, cracking of the SL material has become more likely to occur due to diversification of usage conditions of floors and walls. Moreover, in order to prevent formaldehyde emission from a plywood, the process of mix | blending components, such as paraffin, may be given at the time of plywood preparation, etc., and the transfer | transfer to the surface of paraffin etc. may become a problem. As a result, there is a further increase between the conventional resin emulsion and the plywood, resulting in poor adhesion between the plywood and the SL material.
本発明は0℃以下の樹脂を含む樹脂エマルジョンを硬化性物質と組み合わせ、合板表面に塗布・乾燥することにより、各種SL材の(1)ワレの発生を防止し、(2)優れた合板との密着性を発揮する積層合板を提供することを目的とする。 In the present invention, a resin emulsion containing a resin of 0 ° C. or lower is combined with a curable substance, and applied to the plywood surface and dried to prevent (1) cracking of various SL materials, and (2) excellent plywood and An object of the present invention is to provide a laminated plywood that exhibits the adhesiveness of the above.
本発明は、前記(1)〜(2)の課題を同時に解決するために、特定のガラス転移温度を持つ樹脂エマルジョンと硬化性物質を組み合わせ合板表面に塗布・硬化させた積層合板を見出し、本発明をなすに至った。
すなわち、本発明は、
[1]水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)とガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)とからなる配合物を、合板の少なくとも一方の表面に積層されてなることを特徴とする積層合板、
[2]水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)とガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)との比率は、(1)が100質量部に対し、(2)が5〜50質量部(固形分)であることを特徴とする上記[1]に記載の積層合板、
[3]上記[1]1または[2]記載のガラス転移温度が0℃以下の樹脂含む樹脂エマルジョンが、芳香族ビニル系単量体及び(メタ)アクリル酸エステル単量体から選ばれる1種以上の単量体を含む単量体組成物を乳化重合して得られることを特徴とする積層合板、
である。
In order to solve the above problems (1) to (2) at the same time, the present invention finds a laminated plywood in which a resin emulsion having a specific glass transition temperature and a curable substance are applied and cured on the surface of the plywood. Invented the invention.
That is, the present invention
[1] A composition comprising at least one curable substance (1) selected from a hydraulic substance and a pneumatic substance, and a resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or lower, is added to at least a plywood. Laminated plywood, characterized by being laminated on one surface,
[2] The ratio of at least one curable material (1) selected from hydraulic materials and pneumatic materials to the resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or less is 100 (1). The laminated plywood according to [1] above, wherein (2) is 5 to 50 parts by mass (solid content) with respect to parts by mass,
[3] The resin emulsion containing a resin having a glass transition temperature of 0 ° C. or lower as described in [1] 1 or [2] above is selected from aromatic vinyl monomers and (meth) acrylic acid ester monomers Laminated plywood obtained by emulsion polymerization of a monomer composition containing the above monomers,
It is.
本発明の積層合板は、各種SL材を塗布・硬化させた時、ワレの発生もなく、またSL材と合板との優れた密着性を発現する効果を有する。 The laminated plywood of the present invention has the effect of exhibiting excellent adhesion between the SL material and the plywood without occurrence of cracking when various SL materials are applied and cured.
本発明について、以下具体的に説明する。
本発明に用いられる合板は、JASで規定される各種の合板を指し、特にその種類は限定されない。
本発明に用いられる水硬性物質は、空気中あるいは水中において水和反応により硬化する物質を指し、例えばセメント挙げられる。セメントは例えば、JIS R5210(ポルトランドセメント)、R5211(高炉セメント)、R5212(シリカセメント)、R5213(フライアッシュセメント)に規定されている、普通ポルトランドセメント、早強ポルトランドセメント、超早強ポルトランドセメント、中庸熱ポルトランドセメント、耐硫酸塩ポルトランドセメント、高炉セメント、シリカセメント、フライアッシュセメントが使用でき、また社団法人セメント協会が、セメントの常識(1994年3月発行)に記載している、特殊セメント、白色ポルトランドセメント、セメント系固化材、アルミナセメント、超速硬セメント、コロイドセメント、湯井セメント、地熱井セメント、膨張セメント、その他特殊セメント等種々のセメントを使用できる。
The present invention will be specifically described below.
The plywood used in the present invention refers to various plywoods defined by JAS, and the type is not particularly limited.
The hydraulic substance used in the present invention refers to a substance that hardens by a hydration reaction in air or water, and includes, for example, cement. The cement is defined by, for example, JIS R5210 (Portland cement), R5211 (blast furnace cement), R5212 (silica cement), R5213 (fly ash cement), ordinary Portland cement, early-strength Portland cement, ultra-early-strength Portland cement, Medium-heated Portland cement, sulfate-resistant Portland cement, blast furnace cement, silica cement, fly ash cement can be used, and a special cement described in the common sense of cement (issued in March 1994) by the Japan Cement Association Various cements such as white Portland cement, cement-based solidified material, alumina cement, super-hard cement, colloid cement, Yui cement, geothermal cement, expanded cement, and other special cements can be used.
本発明に用いられる気硬性物質は、空気中の炭酸ガスと反応し硬化する物質であり、また石膏のように水分が蒸発して始めて硬化する物質などを指す。空気中の炭酸ガスと反応し硬化する物質としては石灰系プラスターが挙げられ、例えばJIS A6902に規定する左官用消石灰、JIS A6903に規定するドロマイトプラスターなどが挙げられる。
本発明に用いられるガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョンは、その種類に特に制限はない。例えばアクリル系、アクリル−スチレン系、スチレン−ブタジエン系、アクリロニトリル−ブタジエン系、酢酸ビニル系、エチレン−酢酸ビニル系、ウレタン系、クロロプレン系等が挙げられる。
The air-hardening substance used in the present invention is a substance that cures by reacting with carbon dioxide in the air, and also refers to a substance that hardens only after moisture evaporates, such as gypsum. Examples of the substance that reacts with carbon dioxide in the air and hardens include lime-based plaster, such as plaster slaked lime as defined in JIS A6902, dolomite plaster as defined in JIS A6903, and the like.
The type of the resin emulsion containing a resin having a glass transition temperature of 0 ° C. or lower used in the present invention is not particularly limited. Examples include acrylic, acryl-styrene, styrene-butadiene, acrylonitrile-butadiene, vinyl acetate, ethylene-vinyl acetate, urethane, chloroprene, and the like.
本発明において水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)とガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)との比率は、(1)が100質量部に対し、(2)が5〜50質量部(固形分)である。(1)が100質量部に対し、(2)が5質量部(固形分)以上で耐ワレ性、密着性が良好であり、(2)が50質量部(固形分)以下で耐ワレ性、密着性が良好である。さらに好ましくは、(1)が100質量部に対し、(2)が10〜40質量部(固形分)である。
本発明においてガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)は、芳香族ビニル系単量体及び(メタ)アクリル酸エステル単量体から選ばれる1種以上の単量体を含む単量体組成物を乳化重合して得られるアクリル系エマルジョン、スチレン−アクリル系エマルジョンが好ましい。
In the present invention, the ratio of one or more curable substances (1) selected from hydraulic substances and pneumatic substances to the resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or less is (1) being 100. (2) is 5-50 mass parts (solid content) with respect to mass parts. When (1) is 100 parts by mass, (2) is 5 parts by mass (solid content) or more and crack resistance and adhesion are good, and (2) is 50 parts by mass (solid content) or less and crack resistance. Good adhesion. More preferably, (1) is 10 to 40 parts by mass (solid content) with respect to 100 parts by mass.
In the present invention, the resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or lower contains one or more monomers selected from aromatic vinyl monomers and (meth) acrylic acid ester monomers. An acrylic emulsion obtained by emulsion polymerization of the monomer composition and a styrene-acrylic emulsion are preferred.
芳香族ビニル系単量体としては、例えば、スチレン、ビニルトルエン、α−メチルスチレン、β−メチルスチレン等が挙げられる。好ましくはスチレンである。
(メタ)アクリル酸エステル単量体としては、例えば、メチルアクリレート、エチルアクリレート、プロピルアクリレート、イソプロピルアクリレート、ブチルアクリレート、イソブチルアクリレート、ヘキシルアクリレート、シクロヘキシルアクリレート、2−エチルヘキシルアクリレート、ラウリルアクリレート、ベンジルアクリレート、フェニルアクリレート、メチルメタクリレート、エチルメタクリレート、プロピルメタクリレート、イソプロピルメタクリレート、ブチルメタクリレート、イソブチルメタクリレート、ヘキシルメタクリレート、シクロヘキシルメタクリレート、2−エチルヘキシルメタクリレート、ラウリルメタクリレート、ベンジルメタクリレート、フェニルメタクリレート等が挙げられる。好ましくは、ブチルアクリレート、2−エチルヘキシルアクリレート、メチルメタクリレートである。
Examples of the aromatic vinyl monomer include styrene, vinyl toluene, α-methyl styrene, β-methyl styrene and the like. Styrene is preferred.
Examples of (meth) acrylic acid ester monomers include methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, butyl acrylate, isobutyl acrylate, hexyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate, benzyl acrylate, and phenyl. Examples include acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, butyl methacrylate, isobutyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, lauryl methacrylate, benzyl methacrylate, and phenyl methacrylate. Preferred are butyl acrylate, 2-ethylhexyl acrylate, and methyl methacrylate.
様々な品質・物性を改良するために、上記以外の単量体成分を使用することができる。上記以外の単量体として、例えば(イ)アミド基含有ビニル単量体、(ロ)シアノ基含有ビニル単量体、(ハ)架橋性単量体、(ニ)ヒドロキシル基含有ビニル系単量体、(ホ)不飽和カルボン酸単量体、(ヘ)その他のエチレン性不飽和単量体等を挙げることができる。
乳化重合の方法に関しては特に制限はなく、従来公知の方法を用いることができる。すなわち、水性媒体中で単量体組成物、ラジカル重合開始剤、非反応性界面活性剤、反応性界面活性剤、および必要に応じて用いられる連鎖移動剤等の他の添加剤成分などを基本組成成分とする分散系において、単量体組成物を重合する方法である。そして、重合に際しては、供給する単量体組成物の組成を全重合過程で一定にする方法や重合過程で逐次、あるいは連続的に変化させることによって生成するラテックス粒子の形態的な組成変化を与える方法など所望に応じてさまざまな方法が利用できる。
In order to improve various qualities and physical properties, monomer components other than those described above can be used. Examples of monomers other than those described above include (a) amide group-containing vinyl monomers, (b) cyano group-containing vinyl monomers, (c) crosslinkable monomers, and (d) hydroxyl group-containing vinyl monomers. And (e) an unsaturated carboxylic acid monomer, (f) other ethylenically unsaturated monomers, and the like.
There is no restriction | limiting in particular regarding the method of emulsion polymerization, A conventionally well-known method can be used. That is, based on a monomer composition, a radical polymerization initiator, a non-reactive surfactant, a reactive surfactant, and other additive components such as a chain transfer agent used as necessary in an aqueous medium. This is a method of polymerizing a monomer composition in a dispersion system as a composition component. In the polymerization, the composition of the supplied monomer composition is made constant throughout the entire polymerization process, and the morphological composition change of the latex particles produced is changed by changing the polymerization process sequentially or continuously. Various methods can be used as desired.
本発明において樹脂のガラス転移温度は0℃以下が好ましい。ガラス転移温度が0℃以下で耐ワレ性、合板への密着性が良好である。さらに好ましくは、ガラス転移温度が−10℃〜−60℃である。
本発明で言う重合体のガラス転移温度は、単量体のホモ重合体のガラス転移温度と単量体の共重合比率より次式によって定義することが可能である。
1/Tg=W1/Tg1+W2/Tg2+・・・
Tg:単量体1、2・・・よりなる重合体のガラス転移温度(゜K)
W1、W2・・:単量体1、単量体2、・・の質量分率
ここでW1+W2+・・=1
Tg1、Tg2・・:単量体1、単量体2、・・のホモ重合体のガラス転移温度(゜K)
In the present invention, the glass transition temperature of the resin is preferably 0 ° C. or lower. The glass transition temperature is 0 ° C. or less, and the crack resistance and the adhesion to the plywood are good. More preferably, the glass transition temperature is −10 ° C. to −60 ° C.
The glass transition temperature of the polymer referred to in the present invention can be defined by the following formula from the glass transition temperature of the monomer homopolymer and the copolymerization ratio of the monomer.
1 / Tg = W1 / Tg1 + W2 / Tg2 + ...
Tg: Glass transition temperature (° K) of a polymer comprising monomers 1, 2...
W1, W2...: Mass fraction of monomer 1, monomer 2,..., Where W1 + W2 +.
Tg1, Tg2,...: Glass transition temperature (° K) of homopolymer of monomer 1, monomer 2,.
計算に使用する単量体のホモ重合体のTg(゜K)は、例えばポリマーハンドブック(Jhon Willey & Sons)に記載されている。本願において用いた数値を例示する。カッコ内の値がホモ重合体のTgを示す。ポリスチレン(373゜K)、ポリメチルメタクリレート(378゜K)、ポリブチルアクリレート(219゜K)、ポリ2−エチルヘキシルアクリレート(205゜K)、ポリアクリル酸(379゜K)、ポリメタクリル酸(403゜K)、ポリアクリロニトリル(373゜K)、ポリ2−ヒドロキシエチルアクリレート(258゜K)、ポリ2−ヒドロキシエチルメタクリレート(328゜K)である。 The Tg (° K) of the monomer homopolymer used in the calculation is described in, for example, the polymer handbook (Jhon Willy & Sons). The numerical value used in this application is illustrated. The value in parentheses indicates the Tg of the homopolymer. Polystyrene (373 ° K), polymethyl methacrylate (378 ° K), polybutyl acrylate (219 ° K), poly 2-ethylhexyl acrylate (205 ° K), polyacrylic acid (379 ° K), polymethacrylic acid (403 ° K), polyacrylonitrile (373 ° K), poly-2-hydroxyethyl acrylate (258 ° K), and poly-2-hydroxyethyl methacrylate (328 ° K).
本発明の樹脂エマルジョンには性能を向上させるために、以下の材料を配合してもよい。例えば、水溶性樹脂、溶剤、可塑剤、消泡剤、増粘剤、レベリング剤、分散剤、カップリング剤、着色剤、耐水化剤、潤滑剤、pH調整剤、防腐剤、無機顔料、有機顔料、界面活性剤、架橋剤、例えばエポキシ系化合物、多価金属化合物、イソシアネート系化合物などが挙げられる。また、減水剤及び流動化剤(ポリカルボン酸系、メラミンスルホン酸系、ナフタリンスルホン酸系、リグニンスルホン酸系など)、収縮低減剤(グリコールエーテル系、ポリエーテル系等)、耐寒剤(塩化カルシウム、珪酸塩等)、防水剤(ステアリン酸、シリコン系等)、防錆剤(リン酸塩、亜硝酸塩等)、粘度調整剤(メチルセルロース、ヒドロキシエチルセルロース、ポリビニルアルコール等)、凝結調整剤(リン酸塩等)等を配合してもよい。 In order to improve the performance, the following materials may be blended in the resin emulsion of the present invention. For example, water-soluble resins, solvents, plasticizers, antifoaming agents, thickeners, leveling agents, dispersants, coupling agents, colorants, water resistance agents, lubricants, pH adjusters, preservatives, inorganic pigments, organic Examples include pigments, surfactants, and crosslinking agents such as epoxy compounds, polyvalent metal compounds, and isocyanate compounds. Also, water reducing agents and fluidizing agents (polycarboxylic acid, melamine sulfonic acid, naphthalene sulfonic acid, lignin sulfonic acid, etc.), shrinkage reducing agents (glycol ether, polyether, etc.), cold-resistant agents (calcium chloride) , Silicates, etc.), waterproofing agents (stearic acid, silicones, etc.), rust inhibitors (phosphates, nitrites, etc.), viscosity modifiers (methylcellulose, hydroxyethylcellulose, polyvinyl alcohol, etc.), setting modifiers (phosphoric acid) Salt etc.) may be added.
本発明の水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)とガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)とからなる配合物には、様々な品質・物性を改良するために、充填材、先に挙げた減水剤及び流動化剤(ポリカルボン酸系、メラミンスルホン酸系、ナフタリンスルホン酸系、リグニンスルホン酸系など)、収縮低減剤(グリコールエーテル系、ポリエーテル系等)、耐寒剤(塩化カルシウム、珪酸塩等)、防水剤(ステアリン酸、シリコン系等)、防錆剤(リン酸塩、亜硝酸塩等)、粘度調整剤(メチルセルロース、ヒドロキシエチルセルロース、ポリビニルアルコール等)、凝結調整剤(リン酸塩等)、さらに膨張剤(エトリンガイト系、石灰系等)、着色剤(酸化鉄、酸化クロム等)、消泡剤(シリコン系、鉱油系等)、補強材(鋼繊維、ガラス繊維、合成繊維等)、界面活性剤(アニオン、ノニオン、カチオン系等)、増粘剤、レベリング剤、成膜助剤、溶剤、可塑剤、分散剤、耐水化剤、潤滑剤等が挙げられる。 There are various types of formulations comprising one or more curable substances (1) selected from the hydraulic substance and the pneumatic substance of the present invention and a resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or lower. In order to improve quality and physical properties, fillers, water reducing agents and fluidizing agents mentioned above (polycarboxylic acids, melamine sulfonic acids, naphthalene sulfonic acids, lignin sulfonic acids, etc.), shrinkage reducing agents (glycols) Ether-based, polyether-based, etc.), cold-resistant agents (calcium chloride, silicates, etc.), waterproofing agents (stearic acid, silicon-based, etc.), rust inhibitors (phosphates, nitrites, etc.), viscosity modifiers (methylcellulose, Hydroxyethyl cellulose, polyvinyl alcohol, etc.), setting modifiers (phosphate, etc.), swelling agents (etringite, lime, etc.), colorants (iron oxide, chromium oxide, etc.), antifoaming (Silicone, mineral oils, etc.), reinforcing materials (steel fibers, glass fibers, synthetic fibers, etc.), surfactants (anions, nonions, cationics, etc.), thickeners, leveling agents, film-forming aids, solvents, Examples thereof include a plasticizer, a dispersant, a water resistant agent, and a lubricant.
充填材としては一般的にセメントモルタルに用いられる砂、珪砂、寒水砂、天然及び人工軽量骨材等が使用でき、また無機または有機の顔料等も用いることができ例えば、無機顔料ではマグネシウム、カルシウム、亜鉛、バリウム、チタン、アルミニウム、アンチモン、鉛などの各種金属酸化物、水酸化物、硫化物、炭酸塩、硫酸塩または珪酸化合物などが挙げられる。具体的には例えば、炭酸カルシウム、カオリン、タルク、二酸化チタン、水酸化アルミニウム、シリカ、石膏、バライト粉、アルミナホワイト、サチンホワイトなどである。有機顔料ではポリスチレン、ポリエチレン、ポリ塩化ビニルなどの固体高分子微粉末などが挙げられる。 As fillers, sand, silica sand, cold water sand, natural and artificial lightweight aggregates and the like generally used for cement mortar can be used, and inorganic or organic pigments can also be used. For example, inorganic pigments include magnesium and calcium. , Zinc, barium, titanium, aluminum, antimony, lead and other metal oxides, hydroxides, sulfides, carbonates, sulfates or silicate compounds. Specific examples include calcium carbonate, kaolin, talc, titanium dioxide, aluminum hydroxide, silica, gypsum, barite powder, alumina white, and satin white. Examples of organic pigments include solid polymer fine powders such as polystyrene, polyethylene, and polyvinyl chloride.
本発明において充填材の使用量は、(1)100質量部に対して充填材が5〜500質量部であることが好ましい。充填材5質量部以上で、耐ワレ性、密着性が良好である。一方、500質量部以下で耐ワレ性が良好である。好ましくは50〜400質量部の範囲である。
本発明の積層合板の製造方法に関しては特に制限はなく、従来公知の方法で製造することができる。すなわち、水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)とガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)とからなる配合物を作製し、次いで合板の表面に塗布し、積層する。塗布方法は特に制限はなく、例えば現場では刷毛塗り、コテ塗り、スプレー塗布、ローラー塗布、ブラシ塗布、へら塗り、定規塗り、トンボ塗り等が挙げれ、またラインではロール塗布、カーテン塗布、スプレー塗布等が挙げられる。塗布後、乾燥を行うが、乾燥方法、乾燥条件等も特に制限はなく、室温乾燥、強制乾燥等が挙げられる。
In this invention, it is preferable that the usage-amount of a filler is (1) 5-500 mass parts of fillers with respect to 100 mass parts. With 5 parts by mass or more of filler, cracking resistance and adhesion are good. On the other hand, crack resistance is good at 500 parts by mass or less. Preferably it is the range of 50-400 mass parts.
There is no restriction | limiting in particular regarding the manufacturing method of the laminated plywood of this invention, It can manufacture by a conventionally well-known method. That is, a composition comprising one or more curable substances (1) selected from a hydraulic substance and a pneumatic substance and a resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or lower is prepared, and then plywood Apply to the surface of and laminate. There are no particular restrictions on the application method, and examples include brush coating, trowel coating, spray coating, roller coating, brush coating, spatula coating, ruler coating, and dragonfly coating. Is mentioned. After application, drying is performed, but the drying method, drying conditions, and the like are not particularly limited, and examples include room temperature drying and forced drying.
本発明の水硬性物質及び気硬性物質から選ばれる1種以上の硬化性物質(1)ガラス転移温度が0℃以下の樹脂を含む樹脂エマルジョン(2)とからなる配合物を、合板の表面に直接積層されてもよく、必要に応じて多層構成でもよい。例えば、配合物の下に塗料等の層があってもよい。 One or more curable substances selected from the hydraulic substance and the pneumatic substance of the present invention (1) A composition comprising a resin emulsion (2) containing a resin having a glass transition temperature of 0 ° C. or less is applied to the surface of the plywood. They may be laminated directly, or may have a multilayer structure as necessary. For example, there may be a layer of paint or the like under the formulation.
本発明を実施例に基づいて説明する。本発明の実施態様は、これらによって限定されるものではない。なお、例中の部数はすべて有り姿での部数(即ち、樹脂エマルジョンは水を含有したそのものの部数である)を示した。また、「部」は特に断らない限り「質量部」を示すものである。
[物性の測定]
各特性は次のようにして求めた。
(1)ワレ性:
硬化性物質と樹脂エマルジョンとの配合物を積層した合板を、 JIS A6909(建築用仕上塗材)7.11温冷繰り返し試験条件に樹脂セメントモルタル硬化物を放置し、温冷繰り返し20サイクルを実施した。その後、目視によりワレの判定を行った。
(2)密着性:
a.常態密着 硬化性物質と樹脂エマルジョンとの配合物を積層した合板を、JIS A1171−2000(ポリマーセメントモルタルの試験方法)の7.2接着強さ試験に準拠して、合板と硬化配合物との密着性の測定を行った。
b.温冷サイクル後:硬化性物質と樹脂エマルジョンとの配合物を積層した合板を、 JIS A6909(建築用仕上塗材)7.11温冷繰り返し試験条件に樹脂セメントモルタル硬化物を放置し、温冷繰り返し10サイクルを実施した後、a.と同様に密着性の測定を行った。
The present invention will be described based on examples. However, the embodiments of the present invention are not limited thereto. In addition, all the parts in the examples indicate the number of parts as they are (that is, the resin emulsion is the number of parts containing water itself). “Part” means “part by mass” unless otherwise specified.
[Measurement of physical properties]
Each characteristic was calculated | required as follows.
(1) Cracking property:
Plywood laminated with a mixture of curable substance and resin emulsion is subjected to JIS A6909 (finishing coating material for construction) 7.11 Heated / cooled repeated test conditions, and the cured resin cement mortar is left for 20 cycles of repeated heating and cooling. did. Thereafter, cracking was visually determined.
(2) Adhesion:
a. Normal adhesion A plywood laminated with a compound of a curable substance and a resin emulsion is bonded to a plywood and a cured compound in accordance with 7.2 bond strength test of JIS A1171-2000 (Testing method for polymer cement mortar). Adhesion was measured.
b. After heating / cooling cycle: Plywood laminated with a mixture of a curable substance and a resin emulsion is subjected to JIS A6909 (finishing coating material for construction) 7.11 Repeated testing for heating / cooling, and the cured resin cement mortar is left to cool. After 10 repeated cycles, a. The adhesion was measured in the same manner as described above.
[実施例1〜2]
表1に示す配合を用いて、積層合板を作製した。作製は以下のとおり。市販の合板に、配合物を1.5kg/m2となるよう塗布する。室温で1日乾燥させ、次いで市販セメント系SL材を20kg/m2となるよう塗り継ぎ、養生を2週間行った。
その後、(1)ワレ性、(2)密着性の試験を行った。その結果を表1に示す。
[Examples 1-2]
A laminated plywood was produced using the formulation shown in Table 1. The production is as follows. The compound is applied to a commercially available plywood so as to be 1.5 kg / m 2 . It was dried at room temperature for 1 day, and then a commercial cement-based SL material was applied to 20 kg / m 2 and cured for 2 weeks.
Then, (1) cracking property and (2) adhesion test were performed. The results are shown in Table 1.
[実施例3〜4]
合板表面にパラフィン5%トルエン溶液を、1g/m2となるよう塗布し、パラフィン含有合板のモデル合板を作製した。
このモデル合板を用い、実施例1と同様に表1に示す配合を作製して、積層合板を作製した。また、実施例1と同様に、(1)ワレ性、(2)密着性の試験を行った。その結果を表1に示す。
[Examples 3 to 4]
A paraffin 5% toluene solution was applied to the surface of the plywood so as to be 1 g / m 2 to prepare a model plywood of paraffin-containing plywood.
Using this model plywood, the composition shown in Table 1 was produced in the same manner as in Example 1 to produce a laminated plywood. Further, as in Example 1, (1) cracking property and (2) adhesion test were performed. The results are shown in Table 1.
[比較例1〜3]
実施例3で用いたモデル合板を用い、表2に示す配合を作製して、積層合板を作製した。実施例1と同様に(1)ワレ性、(2)密着性の試験を行った。その結果を表2に示す。
尚、比較例1は樹脂エマルジョンを用いない例であり、比較例2は樹脂エマルジョンのみを用いた例である。比較例3はガラス転移温度10℃の樹脂を含む樹脂エマルジョンを用いた例である。
[Comparative Examples 1-3]
Using the model plywood used in Example 3, the composition shown in Table 2 was produced to produce a laminated plywood. In the same manner as in Example 1, (1) cracking property and (2) adhesion test were performed. The results are shown in Table 2.
Comparative Example 1 is an example in which no resin emulsion is used, and Comparative Example 2 is an example in which only a resin emulsion is used. Comparative Example 3 is an example using a resin emulsion containing a resin having a glass transition temperature of 10 ° C.
本発明の積層合板は、各種SL材を表面に塗布・硬化させることで、床、壁の建築部材の分野で好適に利用できる。それ以外では例えばセメントモルタル、またはポリマーセメントモルタル、セメントペースト、石灰系プラスター、等を表面に塗布・硬化させることもでき、建築用意匠材料として使用できる。 The laminated plywood of the present invention can be suitably used in the field of floor and wall building members by applying and curing various SL materials on the surface. In other cases, for example, cement mortar, polymer cement mortar, cement paste, lime-based plaster, or the like can be applied and cured on the surface, and can be used as a building preparation material.
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