JPH0948090A - Veneer manufacturing method - Google Patents
Veneer manufacturing methodInfo
- Publication number
- JPH0948090A JPH0948090A JP20192295A JP20192295A JPH0948090A JP H0948090 A JPH0948090 A JP H0948090A JP 20192295 A JP20192295 A JP 20192295A JP 20192295 A JP20192295 A JP 20192295A JP H0948090 A JPH0948090 A JP H0948090A
- Authority
- JP
- Japan
- Prior art keywords
- decorative
- wood
- thermosetting resin
- curable composition
- sheet
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 30
- 239000000463 material Substances 0.000 claims abstract description 119
- 239000002023 wood Substances 0.000 claims abstract description 117
- 239000000203 mixture Substances 0.000 claims abstract description 73
- 229920005989 resin Polymers 0.000 claims abstract description 69
- 239000011347 resin Substances 0.000 claims abstract description 69
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 65
- 238000000034 method Methods 0.000 claims abstract description 25
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 24
- 239000003505 polymerization initiator Substances 0.000 claims abstract description 23
- 239000012466 permeate Substances 0.000 claims abstract description 17
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 13
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 13
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 10
- 150000008065 acid anhydrides Chemical class 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000003825 pressing Methods 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 2
- 150000007519 polyprotic acids Polymers 0.000 claims description 2
- 238000005299 abrasion Methods 0.000 abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 11
- 238000002156 mixing Methods 0.000 description 26
- 239000000123 paper Substances 0.000 description 18
- 238000000465 moulding Methods 0.000 description 14
- 238000004898 kneading Methods 0.000 description 9
- 238000007598 dipping method Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 7
- 239000002537 cosmetic Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 238000007731 hot pressing Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- -1 chaff Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 229920002678 cellulose Polymers 0.000 description 4
- 235000010980 cellulose Nutrition 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 3
- LSWYGACWGAICNM-UHFFFAOYSA-N 2-(prop-2-enoxymethyl)oxirane Chemical compound C=CCOCC1CO1 LSWYGACWGAICNM-UHFFFAOYSA-N 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 239000011120 plywood Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- HCXVPNKIBYLBIT-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 3,5,5-trimethylhexaneperoxoate Chemical compound CC(C)(C)CC(C)CC(=O)OOOC(C)(C)C HCXVPNKIBYLBIT-UHFFFAOYSA-N 0.000 description 2
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 2
- KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 2
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 2
- UBRWPVTUQDJKCC-UHFFFAOYSA-N 1,3-bis(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC(C(C)(C)OOC(C)(C)C)=C1 UBRWPVTUQDJKCC-UHFFFAOYSA-N 0.000 description 2
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 2
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 2
- CVIDTCAFIMQJAZ-UHFFFAOYSA-N 4,5,6-tris(tert-butylperoxy)triazine Chemical compound CC(C)(C)OOC1=NN=NC(OOC(C)(C)C)=C1OOC(C)(C)C CVIDTCAFIMQJAZ-UHFFFAOYSA-N 0.000 description 2
- 241000609240 Ambelania acida Species 0.000 description 2
- 241000218691 Cupressaceae Species 0.000 description 2
- 241000196324 Embryophyta Species 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
- 239000010905 bagasse Substances 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 2
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 2
- 229960001826 dimethylphthalate Drugs 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000010902 straw Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 2
- 239000010875 treated wood Substances 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- AYMDJPGTQFHDSA-UHFFFAOYSA-N 1-(2-ethenoxyethoxy)-2-ethoxyethane Chemical compound CCOCCOCCOC=C AYMDJPGTQFHDSA-UHFFFAOYSA-N 0.000 description 1
- KUAOCBMZHIQAQE-UHFFFAOYSA-N 2,4,4-trimethylpentoxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOCC(C)CC(C)(C)C KUAOCBMZHIQAQE-UHFFFAOYSA-N 0.000 description 1
- IFXDUNDBQDXPQZ-UHFFFAOYSA-N 2-methylbutan-2-yl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CC IFXDUNDBQDXPQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Chemical class 0.000 description 1
- 241000218645 Cedrus Species 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical class CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 241000218652 Larix Species 0.000 description 1
- 235000005590 Larix decidua Nutrition 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Chemical class 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 229920006225 ethylene-methyl acrylate Polymers 0.000 description 1
- 229920005680 ethylene-methyl methacrylate copolymer Polymers 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000012978 lignocellulosic material Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229940098458 powder spray Drugs 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Laminated Bodies (AREA)
Abstract
(57)【要約】
【目的】 優れた美観を有し、かつ表面硬度や耐摩耗性
および耐水性などに優れた化粧板を工業的に有利に製造
する方法を提供すること。
【構成】 化学修飾木質材、熱硬化性樹脂および重合開
始剤から成る硬化性組成物を木質基材上に載置し、さら
にその上に未硬化状態の熱硬化性樹脂が浸透、透過しう
る化粧材を載置して、熱圧する。さらに、より好ましく
は化学修飾木質材、熱可塑性樹脂、熱硬化性樹脂および
重合開始剤から成る組成物をシート化し、次いで、得ら
れたシート状の硬化性組成物を木質基材に載置し、さら
にその上に未硬化状態の熱硬化性樹脂が浸透、透過しう
る化粧材を載置して熱圧する。(57) [Summary] [Object] To provide a method for industrially advantageously producing a decorative sheet having an excellent aesthetic appearance and excellent surface hardness, abrasion resistance, and water resistance. [Structure] A curable composition comprising a chemically modified wood material, a thermosetting resin and a polymerization initiator is placed on a wood base material, on which an uncured thermosetting resin can penetrate and permeate. Place the decorative material and heat it. Furthermore, more preferably, a composition comprising a chemically modified wood material, a thermoplastic resin, a thermosetting resin and a polymerization initiator is formed into a sheet, and then the obtained sheet-shaped curable composition is placed on a wood base material. Further, a decorative material through which the uncured thermosetting resin can permeate and permeate is placed thereon and hot pressed.
Description
【0001】[0001]
【産業上の利用分野】本発明は、優れた美観を有し、か
つ表面硬度や耐摩耗性および耐水性などに優れた化粧板
を工業的に有利に製造する方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for industrially producing a decorative board having an excellent appearance and excellent surface hardness, abrasion resistance and water resistance.
【0002】[0002]
【従来の技術】従来、木材の美観、表面硬度、耐摩耗性
および耐水性などを向上させるために、木材に熱硬化性
樹脂を減圧または加圧下で含浸させ、加熱硬化せしめ
る、いわゆるWPC(Wood Plastic Combination)処理す
る方法が知られている。しかしながら、このWPC処理
は工程が繁雑で、設備が大がかりとなり製造費が高くつ
くという欠点があった。また、得られた処理木材の表面
には十分な表面硬度、耐摩耗性をもたらすほどの樹脂膜
層が形成されないという問題があった。また、木材の表
面に熱硬化性樹脂を含浸させた紙、不織布、あるいは、
布等ををオーバーレイする方法がある。しかしながら、
この方法では紙、不織布、あるいは、布等に含浸された
樹脂の流動性が悪く、道管や仮道管の大きな木材では、
接着が不良となり、浮き現象が生じるなどの問題があっ
た。さらに、木材表面を直接、熱硬化性樹脂で被覆する
方法がある。この方法は道管、仮道管の大きな木材、あ
るいは、その表面が粗面となっているような木材の表面
を被覆するのに好適である。しかしながら、熱硬化性樹
脂の硬化を熱圧によって行おうとした場合、熱硬化性樹
脂の架橋による硬化が始まる前に、熱硬化性樹脂の急激
な粘度低下を伴うために、該熱硬化性樹脂が木材の側面
から外部に流出するという欠点があった。また、得られ
る処理木材の表面の樹脂層の耐クラック性が悪く、割れ
を生じやすいという欠点を有していた。2. Description of the Related Art Conventionally, in order to improve the aesthetics, surface hardness, abrasion resistance and water resistance of wood, so-called WPC (Wood) is used in which wood is impregnated with a thermosetting resin under reduced pressure or pressure and heat-cured. Plastic Combination) processing method is known. However, this WPC process has a drawback that the process is complicated, the equipment is large, and the manufacturing cost is high. In addition, there is a problem that a resin film layer having sufficient surface hardness and abrasion resistance is not formed on the surface of the obtained treated wood. In addition, paper, non-woven fabric, which is made by impregnating the surface of wood with thermosetting resin, or
There is a method of overlaying cloth etc. However,
With this method, the fluidity of the resin impregnated in paper, non-woven fabric, or cloth is poor, and with large timbers such as conduits and temporary conduits,
There were problems such as poor adhesion and floating phenomenon. Further, there is a method of directly coating the wood surface with a thermosetting resin. This method is suitable for coating a large piece of wood such as a conduit or a temporary conduit, or a surface of wood having a rough surface. However, when the thermosetting resin is to be cured by heat and pressure, the thermosetting resin is rapidly reduced in viscosity before the curing by the crosslinking of the thermosetting resin is started. There was a drawback that it leaked out from the side of the wood. Further, the resin layer on the surface of the obtained treated wood has poor crack resistance and has a drawback that cracking is likely to occur.
【0003】また、特公平7-35109号 にはプリントコー
ト紙の裏面と木質基材との間にシート状に形成された熱
硬化性樹脂材を介在させ、熱圧して前記熱硬化性樹脂材
を介してプリントコート紙と木質基材とを固着させる複
合板の製造方法が開示されている。この方法は、熱圧
時、粘度低下を起こす熱硬化性樹脂がプリントコート紙
の表面にしみ出し、装置周辺を汚染するのを避けるため
に、プリントコート紙を用いることを特徴としている。
しかしながら、この方法によってもやはり粘度低下を起
こした硬化性樹脂が木質基材の側面から外部に流出する
ことは避けられなかった。Further, in Japanese Patent Publication No. 7-35109, a thermosetting resin material formed in a sheet shape is interposed between the back surface of the print coated paper and the wood base material, and the thermosetting resin material is heated and pressed. A method of manufacturing a composite board is disclosed in which a print-coated paper and a wood-based material are fixed to each other via a sheet. This method is characterized in that the print coated paper is used in order to prevent the thermosetting resin, which causes a decrease in viscosity when hot pressed, from seeping out to the surface of the print coated paper and contaminating the periphery of the apparatus.
However, even with this method, it was unavoidable that the curable resin, which had decreased in viscosity, also flowed out from the side surface of the wooden base material.
【0004】[0004]
【発明が解決しようとする課題】本発明は、上記したよ
うな状況に鑑み、木質板材、とりわけ、美観的に十分で
ない、あるいは、表面硬度の低い木質板材と化粧紙、化
粧単板等(以下化粧材と称する)との間に、硬化性組成
物を載置し、熱圧することにより、優れた美観を有し、
かつ表面硬度、耐摩耗性および耐水性などに優れた化粧
板を工業的に有利に製造する方法を提供することをその
目的とする。SUMMARY OF THE INVENTION In view of the above situation, the present invention provides a wood board material, particularly a wood board material that is not aesthetically sufficient or has a low surface hardness, a decorative paper, a decorative veneer, etc. It has an excellent aesthetics by placing a curable composition between it and a hot press.
It is an object of the present invention to provide a method for industrially advantageously manufacturing a decorative sheet having excellent surface hardness, abrasion resistance, water resistance and the like.
【0005】[0005]
【課題を解決するための手段】本発明者らは、上記課題
を解決する方法につき鋭意研究を行った。この結果、化
学修飾木質材、熱硬化性樹脂および重合開始剤を添加混
合した硬化性組成物を、木質基材と化粧材の間に位置さ
せ、硬化性組成物中の化学修飾木質材が可塑化するのに
必要な圧力を以て熱圧することにより、該硬化性組成物
中の化学修飾木質材の可塑化と、熱硬化性樹脂の架橋を
行わせしめ、これらによって木質基材と化粧材を一体化
させると同時に、主として該硬化性組成物中の熱硬化性
樹脂を化粧材に浸透、透過、さらに反対の面にまでしみ
出させ、そして硬化せしめることにより、優れた美観を
有し、しかも、表面硬度、耐摩耗性および耐水性に優れ
た化粧板が得られることを見い出し、本発明を完成する
に至った。[Means for Solving the Problems] The inventors of the present invention have conducted extensive studies on a method for solving the above problems. As a result, the curable composition in which the chemically modified wood material, the thermosetting resin and the polymerization initiator were added and mixed was placed between the wood base material and the decorative material, and the chemically modified wood material in the curable composition was plasticized. By heat-pressing with the pressure necessary for the curing, the chemically modified wood material in the curable composition is plasticized and the thermosetting resin is cross-linked, thereby integrating the wood base material and the decorative material. At the same time, the thermosetting resin in the curable composition has an excellent aesthetic appearance by permeating the cosmetic material into the cosmetic material, permeating the cosmetic material, exuding to the opposite surface, and curing. It has been found that a decorative board excellent in hardness, abrasion resistance and water resistance can be obtained, and the present invention has been completed.
【0006】即ち本発明によれば、化学修飾木質材、熱
硬化性樹脂および重合開始剤から成る硬化性組成物を木
質基材上に載置し、さらにその上に未硬化状態の熱硬化
性樹脂が浸透、透過しうる化粧材を載置して、熱圧する
ことを特徴とする化粧板の製造方法が提供され、また、
より好ましくは、化学修飾木質材、熱可塑性樹脂、熱硬
化性樹脂および重合開始剤から成るシート状の硬化性組
成物を木質基材に載置し、さらにその上に未硬化状態の
熱硬化性樹脂が浸透、透過しうる化粧材を載置して、熱
圧することを特徴とする化粧板の製造方法が提供され、
また、未硬化状態の熱硬化性樹脂が浸透、透過しうる化
粧材が普通化粧紙、あるいは、化粧単板であることを特
徴とする化粧板の製造方法が提供され、また、熱可塑性
樹脂が、化学修飾木質材100重量部に対して1〜20
重量部添加混合されたことを特徴とする化粧板の製造方
法が提供され、また、より好ましくは、熱可塑性樹脂
が、エチレン−酢酸ビニル共重合体であることを特徴と
する化粧板の製造方法が提供され、また、熱硬化性樹脂
が、化学修飾木質材100重量部に対して1〜60重量
部添加混合されたことを特徴とする化粧板の製造方法が
提供され、また、より好ましくは、熱硬化性樹脂が、不
飽和ポリエステル樹脂であることを特徴とする化粧板の
製造方法が提供され、また、化学修飾木質材が、木質材
に多塩基酸無水物およびエポキシ化合物を反応させて得
られるオリゴエステル化木質材であることを特徴とする
化粧板の製造方法が提供され、また、より好ましくは、
オリゴエステル化木質材の製造段階において、熱可塑性
樹脂を添加混合し、得られたオリゴエステル化木質材と
熱可塑性樹脂との混合物に熱硬化性樹脂および重合開始
剤を添加混合し、シート化することによりシート状の硬
化性組成物を得ることを特徴とする化粧板の製造方法が
提供される。That is, according to the present invention, a curable composition comprising a chemically modified wood material, a thermosetting resin and a polymerization initiator is placed on a wood base material, and further, an uncured thermosetting composition is placed thereon. Provided is a method for manufacturing a decorative board, which comprises placing a decorative material through which a resin penetrates and permeates, and applying heat.
More preferably, a sheet-shaped curable composition comprising a chemically modified wood material, a thermoplastic resin, a thermosetting resin and a polymerization initiator is placed on a wood base material, and the uncured thermosetting composition is further placed thereon. A method for manufacturing a decorative board is provided, in which a resin-penetrating or permeable cosmetic material is placed and hot pressed.
Further, there is provided a method for producing a decorative board, characterized in that the decorative material which can be penetrated and penetrated by the uncured thermosetting resin is ordinary decorative paper or a decorative veneer, and the thermoplastic resin is , 1 to 20 per 100 parts by weight of chemically modified wood
Provided is a method for producing a decorative board characterized by being mixed by adding parts by weight, and more preferably, the thermoplastic resin is an ethylene-vinyl acetate copolymer, and a method for producing a decorative board. And a thermosetting resin is added and mixed in an amount of 1 to 60 parts by weight with respect to 100 parts by weight of the chemically modified wood material, and a method for manufacturing a decorative board is provided, and more preferably , A thermosetting resin is an unsaturated polyester resin, a method for manufacturing a decorative board, characterized in that the chemically modified wood material, the wood material is reacted with a polybasic acid anhydride and an epoxy compound. There is provided a method for producing a decorative board, which is characterized in that it is an oligoesterified wood material, and more preferably,
At the production stage of the oligoesterified wood material, a thermoplastic resin is added and mixed, and the resulting mixture of the oligoesterified wood material and the thermoplastic resin is added and mixed with a thermosetting resin and a polymerization initiator to form a sheet. Thus, a method for producing a decorative board is provided, which comprises obtaining a sheet-shaped curable composition.
【0007】本発明で用いられる化学修飾木質材とは、
木質材中の水酸基に化学物質を反応させたものであっ
て、この化学物質の種類と量によっては、木質材そのも
のには本来備わっていなかった熱可塑性を付与すること
ができる。本発明においては化学修飾木質材のうち熱可
塑性が高いものを使用するのが好ましい。これらの例と
しては、特開昭57-103804号、特開昭60-206602号、特開昭
58-32807号、特開昭60-188401号、 白石信夫:木材学会誌
vol.32,No.10,P755-762(1986)、大越誠 :木材学会誌vo
l.36,No.1,P57-63(1990)、等において開示されたエステ
ル化木材、エーテル化木材、アセチル化木材、アリル化
木材、ベンジル化木材、ラウロイル化木材、エチル化木
材、シアノエチル化木材、さらに、特開平2-145339号に
おいて開示されている木質成分中の水酸基に二塩基酸無
水物および重合性二重結合を有するモノエポキシ化合物
を反応させたオリゴエステル化木材、またさらに、アセ
チルセルロース、エチルセルロース、カルボキシメチル
セルロース等のセルロース誘導体等を用いることができ
る。これらの化学修飾木質材のうちでも、製造工程が簡
単で、反応後、系から除去する必要がある副生物がない
という理由から、オリゴエステル化木質材が特に好適に
用いられる。The chemically modified wood material used in the present invention is
A chemical substance is made to react with the hydroxyl group in the wood material, and depending on the type and amount of this chemical material, it is possible to impart thermoplasticity that was not originally provided in the wood material itself. In the present invention, it is preferable to use a chemically modified wood material having high thermoplasticity. Examples of these include JP-A-57-103804, JP-A-60-206602, and JP-A-60-206602.
58-32807, JP-A-60-188401, Nobuo Shiraishi: Journal of the Wood Research Society
vol.32, No.10, P755-762 (1986), Makoto Ogoshi: Journal of the Wood Research Society vo
L.36, No.1, P57-63 (1990), etc., esterified wood, etherified wood, acetylated wood, allylated wood, benzylated wood, lauroylated wood, ethylated wood, cyanoethylated wood Wood, further, oligoesterified wood obtained by reacting a hydroxyl group in a wood component with a dibasic acid anhydride and a monoepoxy compound having a polymerizable double bond disclosed in JP-A-2-145339, and further, acetyl. Cellulose, ethyl cellulose, carboxymethyl cellulose, and other cellulose derivatives can be used. Among these chemically modified wood materials, oligoesterified wood materials are particularly preferably used because the production process is simple and there are no by-products that need to be removed from the system after the reaction.
【0008】一方、化学修飾木質材の原料となる木質材
に関しては、樹種や形状に特に制限はなく、木粉、木材
繊維、木材チップ等の木材を粉砕したものが使用可能で
あるし、セルロース、パルプ等も使用可能である。さら
には、未利用のまま大量に廃棄される麦わら、稲わら、
もみがら、古紙、リンター、バガス等の植物繊維、ある
いは、その他のセルロースやリグニンを主成分とするリ
グノセルロース材料を粉砕したもの等も使用可能であ
る。On the other hand, with respect to the wood material which is a raw material of the chemically modified wood material, there is no particular limitation on the species and shape of the wood material, and wood powder such as wood powder, wood fiber and wood chips can be used, and cellulose can be used. , Pulp, etc. can also be used. Furthermore, a large amount of unused straw, rice straw,
It is also possible to use plant fibers such as chaff, waste paper, linters and bagasse, or other crushed lignocellulosic materials containing cellulose or lignin as a main component.
【0009】熱硬化性樹脂としては、不飽和ポリエステ
ル樹脂、ユリア樹脂、メラミン樹脂、フェノール樹脂、
ケイ素樹脂、エポキシ樹脂、ポリウレタン樹脂、ジアリ
ルフタレート樹脂などが使用可能である。As the thermosetting resin, unsaturated polyester resin, urea resin, melamine resin, phenol resin,
Silicon resin, epoxy resin, polyurethane resin, diallyl phthalate resin, etc. can be used.
【0010】一方、重合開始剤としては公知の有機過酸
化物が使用でき、例えば、:ビス−3,5,5−トリメチ
ルヘキサノイルパーオキサイド、ラウロイルパーオキサ
イド、p−ベンゾイルパーオキサイド、等のジアシルパ
ーオキサイド:ジクミルパーオキサイド、2,5−ジメ
チル−2,5−ジ−(t−ブチルパーオキシ)−ヘキサ
ン、 1,3−ビス−(t−ブチルパーオキシ−イソプロ
ピル)−ベンゼン、t−ブチルクミルパーオキサイド、
ジ−t−ブチルパーオキサイド、2,5− ジメチル−
2,5−ジ−(t−ブチルパーオキシ)−ヘキセン−
3、トリス−(t− ブチルパーオキシ)トリアジン等
のジアルキルパーオキサイド:2,4,4−トリメチルペ
ンチルパーオキシ2−エチルヘキサノエート、t−アミ
ルパーオキシ2−エチルヘキサノエート、t−ブチルパ
ーオキシ−2−エチルヘキサノエート、t−ブチルパー
オキシ−イソブチレート、ジ−t−ブチルパーオキシ−
ヘキサヒドロテレフタレート、t−ブチルパーオキシ
3,5,5−トリメチルヘキサノエート、t−ブチルパー
オキシアセテート、t−ブチルパーオキシベンゾエー
ト、ジ−t−ブチルパーオキシ−トリメチル−アジペー
ト等のアルキルパーエステル:ジ−3−メトキシブチル
パーオキシジカーボネート、ジ−2−エチルヘキシルパ
ーオキシジカーボネート、ビス(4−t−ブチルシクロ
ヘキシル)パーオキシジカーボネート、ジイソプロピル
パーオキシジカーボネート、t−ブチルパーオキシイソ
プロピルカーボネート等のパーカーボネート等が単独
で、あるいは、複数種組み合わせて使用可能である。そ
の配合量は熱硬化性樹脂100重量部に対して、0.1
〜20重量部、さらに好ましくは1.0〜10重量部で
ある。On the other hand, known organic peroxides can be used as the polymerization initiator, and examples thereof include: diacyl such as: bis-3,5,5-trimethylhexanoyl peroxide, lauroyl peroxide and p-benzoyl peroxide. Peroxide: dicumyl peroxide, 2,5-dimethyl-2,5-di- (t-butylperoxy) -hexane, 1,3-bis- (t-butylperoxy-isopropyl) -benzene, t- Butyl cumyl peroxide,
Di-t-butyl peroxide, 2,5-dimethyl-
2,5-di- (t-butylperoxy) -hexene-
3, dialkyl peroxides such as tris- (t-butylperoxy) triazine: 2,4,4-trimethylpentylperoxy 2-ethylhexanoate, t-amylperoxy 2-ethylhexanoate, t-butyl Peroxy-2-ethylhexanoate, t-butylperoxy-isobutyrate, di-t-butylperoxy-
Alkyl peresters such as hexahydroterephthalate, t-butylperoxy 3,5,5-trimethylhexanoate, t-butylperoxyacetate, t-butylperoxybenzoate, di-t-butylperoxy-trimethyl-adipate : Di-3-methoxybutyl peroxydicarbonate, di-2-ethylhexyl peroxydicarbonate, bis (4-t-butylcyclohexyl) peroxydicarbonate, diisopropyl peroxydicarbonate, t-butyl peroxyisopropyl carbonate, etc. These percarbonates and the like can be used alone or in combination of two or more kinds. The blending amount is 0.1 with respect to 100 parts by weight of the thermosetting resin.
To 20 parts by weight, and more preferably 1.0 to 10 parts by weight.
【0011】なお、後述するように、本発明において
は、より好ましい実施形態として、化学修飾木質材、熱
可塑性樹脂、熱硬化性樹脂および重合開始剤から成る硬
化性組成物をあらかじめシート化し、次いで得られたシ
ート状の硬化性組成物を木質基材に接触させ、さらにそ
の上に化粧材を載置して熱圧する。この方法を用いる際
には、化学修飾木質材、熱可塑性樹脂、熱硬化性樹脂、
重合開始剤を添加混合してシート状とする工程におい
て、重合開始剤が分解しにくい方が好ましい。この意味
から、ジクミルパーオキサイド、2,5−ジメチル−2,
5−ジ−(t−ブチルパーオキシ)−ヘキサン、 1,3
−ビス−(t−ブチルパーオキシ−イソプロピル)−ベ
ンゼン、t−ブチルクミルパーオキサイド、ジ−t−ブ
チルパーオキサイド、2,5−ジメチル−2,5−ジ−
(t−ブチルパーオキシ)−ヘキセン−3、トリス−
(t−ブチルパーオキシ)トリアジン、t−ブチルパー
オキシ 3,5, 5−トリメチルヘキサノエート、t−ブ
チルパーオキシアセテート、t−ブチルパーオキシベン
ゾエート、t−ブチルパーオキシイソプロピルカーボネ
ート等、1分間での半減期温度が140℃以上のものが
より好適に用いられる。As will be described later, in the present invention, as a more preferred embodiment, a curable composition comprising a chemically modified wood material, a thermoplastic resin, a thermosetting resin and a polymerization initiator is formed into a sheet in advance, and then, The obtained sheet-shaped curable composition is brought into contact with a wooden base material, and a decorative material is placed thereon and hot pressed. When using this method, chemically modified wood material, thermoplastic resin, thermosetting resin,
In the step of adding and mixing the polymerization initiator to form a sheet, it is preferable that the polymerization initiator is less likely to decompose. From this meaning, dicumyl peroxide, 2,5-dimethyl-2,
5-di- (t-butylperoxy) -hexane, 1,3
-Bis- (t-butylperoxy-isopropyl) -benzene, t-butylcumyl peroxide, di-t-butyl peroxide, 2,5-dimethyl-2,5-di-
(T-Butylperoxy) -hexene-3, tris-
(T-butylperoxy) triazine, t-butylperoxy 3,5,5-trimethylhexanoate, t-butylperoxyacetate, t-butylperoxybenzoate, t-butylperoxyisopropyl carbonate, etc. for 1 minute Those having a half-life temperature of 140 ° C. or higher are more preferably used.
【0012】本発明において木質基材に熱圧、積層され
る化粧材としては、未硬化状態の熱硬化性樹脂が浸透、
透過しうるものであればよく、その代表的なものとし
て、普通化粧紙(未処理化粧紙)、突き板、化粧単板、
不織布などが挙げられる。これらのうちでも、美的観点
から普通化粧紙、化粧単板が特に好適に用いられる。ま
た、木質基材としては、その樹種を問わず、さらに、木
材から直接切り出された板、合板、パーティクルボー
ド、ファイバーボード、OSB、集成材、LVL、およ
びバガス、モミガラなどから成形された植物繊維系木質
基材であるかを問わず、あらゆる木質板が使用可能であ
るが、カラマツ、スギ、ヒノキ、シナ、ホウ、カツラな
どの表面の軟らかい樹木、木目柄の不鮮明な樹木から得
られる木質板が本発明の効果をより有効的に享受でき
る。また、上記木質基材に前もってモノマー、プレポリ
マー、ポリマーなどを注入したもの、あるいは注入後、
さらに硬化させたものを用いることもできる。In the present invention, an uncured thermosetting resin is infiltrated as a decorative material which is hot-pressed and laminated on a wood base material,
Any transparent material may be used, and typical ones include plain decorative paper (untreated decorative paper), veneer, decorative veneer,
Examples include non-woven fabric. Among these, plain decorative paper and decorative veneer are particularly preferably used from the aesthetic point of view. Further, as the wood base material, regardless of the tree species, further, plant fibers directly formed from wood, plywood, particle board, fiber board, OSB, laminated wood, LVL, bagasse, chaff, etc. Any wood board can be used regardless of whether it is a wood-based material, but wood boards obtained from trees with soft surfaces such as larch, cedar, cypress, cypress, hou, and wigs, and trees with unclear grain patterns. Can more effectively enjoy the effect of the present invention. In addition, a monomer, prepolymer, polymer, etc. previously injected into the above-mentioned wood base material, or after injection,
It is also possible to use a cured product.
【0013】また、後述するように、本発明において
は、より好ましい実施形態として、化学修飾木質材、熱
可塑性樹脂、熱硬化性樹脂および重合開始剤から成る硬
化性組成物をあらかじめシート化し、次いで得られたシ
ート状の硬化性組成物を木質基材に載置し、さらにその
上に未硬化状態の熱硬化性樹脂が浸透、透過しうる化粧
材を載置して熱圧する。ここにおいて用いられる熱可塑
性樹脂としては、低密度ポリエチレン、高密度ポリエチ
レン、直鎖状低密度ポリエチレン、超低密度ポリエチレ
ン、ポリプロピレン、ポリブテン−1、エチレン−酢酸
ビニル共重合体、ポリエチレンオキサイドやメタクリル
酸メチル−ブタジエン−スチレン共重合体、軟質ポリ塩
化ビニル、エチレン−エチルアクリレート共重合体、エ
チレン−エチルアクリレート−無水マレイン酸共重合
体、エチレン−アクリル酸共重合体、エチレン−メチル
アクリレート共重合体、エチレン−メチルメタアクリレ
ート共重合体、熱可塑性ポリウレタン、アイオノマー、
芳香族ポリエステル、脂肪族ポリエステル等が挙げら
れ、これらが単独で、あるいは、複数種ブレンドされて
使用される。本発明において用いられる熱可塑性樹脂
は、化学修飾木質材、熱硬化性樹脂、重合開始剤を効率
よく包含でき、さらに、重合開始剤の分解を避けること
ができる温度で混練できるものが好ましい。この意味か
ら、上記熱可塑性樹脂の中でもビカット軟化点が120
℃以下のものがより好ましく、さらにはビカット軟化点
が90℃以下のエチレン−酢酸ビニル共重合体がより好
ましく、またさらには、酢酸ビニル含量が10〜50重
量%のエチレン−酢酸ビニル共重合体が、ビカット軟化
点が80℃以下であるためより好ましい。なお、熱可塑
性樹脂の配合量は化学修飾木質材100重量部に対して
1〜20重量部であることが、さらには好ましくは2〜
10重量部であることが望ましい。熱可塑性樹脂の配合
量が1〜20重量部の範囲内であれば化学修飾木質材、
熱硬化性樹脂、重合開始剤と混合し、シート化する際、
これらを効率よく包含でき、さらに得られる化粧板の耐
熱変形性を損なわず好ましい。As will be described later, in the present invention, as a more preferred embodiment, a curable composition comprising a chemically modified wood material, a thermoplastic resin, a thermosetting resin and a polymerization initiator is formed into a sheet in advance, and then, The obtained sheet-shaped curable composition is placed on a wood-based substrate, and a decorative material through which an uncured thermosetting resin can permeate and permeate is further placed thereon and hot pressed. Examples of the thermoplastic resin used here include low-density polyethylene, high-density polyethylene, linear low-density polyethylene, ultra-low-density polyethylene, polypropylene, polybutene-1, ethylene-vinyl acetate copolymer, polyethylene oxide and methyl methacrylate. -Butadiene-styrene copolymer, soft polyvinyl chloride, ethylene-ethyl acrylate copolymer, ethylene-ethyl acrylate-maleic anhydride copolymer, ethylene-acrylic acid copolymer, ethylene-methyl acrylate copolymer, ethylene -Methyl methacrylate copolymer, thermoplastic polyurethane, ionomer,
Aromatic polyesters, aliphatic polyesters, etc. may be mentioned, and these may be used alone or in a mixture of plural kinds. The thermoplastic resin used in the present invention is preferably one that can efficiently contain a chemically modified wood material, a thermosetting resin, and a polymerization initiator, and that can be kneaded at a temperature at which decomposition of the polymerization initiator can be avoided. From this meaning, the Vicat softening point is 120 among the above thermoplastic resins.
C. or less, more preferably a Vicat softening point of 90.degree. C. or less, more preferably an ethylene-vinyl acetate copolymer, and further, an ethylene-vinyl acetate copolymer having a vinyl acetate content of 10 to 50% by weight. However, it is more preferable because the Vicat softening point is 80 ° C. or lower. The blending amount of the thermoplastic resin is 1 to 20 parts by weight, more preferably 2 to 100 parts by weight of the chemically modified wood material.
It is preferably 10 parts by weight. If the blending amount of the thermoplastic resin is within the range of 1 to 20 parts by weight, the chemically modified wood material,
When mixed with a thermosetting resin and a polymerization initiator to form a sheet,
These are preferable because they can be included efficiently and the resulting decorative plate does not impair the heat distortion resistance.
【0014】その他本発明においては、硬化性組成物の
硬化特性、および、硬化物の特性を低下させない範囲内
において該硬化性組成物に公知の可塑剤、内部離型剤、
無機充填剤、難燃剤、抗菌剤、顔料、染料、酸化防止
剤、紫外線吸収剤、光安定剤、香料等を配合することを
妨げるものではない。Others In the present invention, the curing characteristics of the curable composition, and a plasticizer, an internal release agent, known to the curable composition within a range that does not deteriorate the characteristics of the cured composition,
It does not prevent the compounding of inorganic fillers, flame retardants, antibacterial agents, pigments, dyes, antioxidants, ultraviolet absorbers, light stabilizers, fragrances and the like.
【0015】次いで、本発明の化粧板の製造方法の具体
的製造手順について説明する。まず、化学修飾木質材
に、熱硬化性樹脂および重合開始剤を添加混合し、硬化
性組成物を調製する。これらを混合する手段は特に限定
されるものでなく例えば、ブレンダー、ニーダー、ミキ
シングロール、バンバリーミキサーなどの混練機、ある
いは、単軸、二軸押出機を用いて行うことができる。な
お、混練作業の作業性を良好なものとするため熱硬化性
樹脂の粘度を低下させたい場合には、重合開始剤の分解
が起こらない程度の加温を行ってもよい。Next, a specific manufacturing procedure of the method for manufacturing a decorative board of the present invention will be described. First, a thermosetting resin and a polymerization initiator are added to and mixed with a chemically modified wood material to prepare a curable composition. The means for mixing these is not particularly limited, and for example, a kneader such as a blender, a kneader, a mixing roll, a Banbury mixer, or a single-screw or twin-screw extruder can be used. When it is desired to reduce the viscosity of the thermosetting resin in order to improve the workability of the kneading work, heating may be performed to such an extent that decomposition of the polymerization initiator does not occur.
【0016】また、本発明においては、より好ましい実
施形態として、化学修飾木質材、熱硬化性樹脂、重合開
始剤、および熱可塑性樹脂から成るシート状の硬化性組
成物が用いられる。このように熱可塑性樹脂がつけ加え
られることにより硬化性組成物の混練が非常に有効にな
されるとともに、シートの厚み調整も比較的容易である
ことから、得られるシート状の硬化性組成物の厚みの均
一性が良好なものとなる。従って、木質基材に該シート
状の硬化性組成物を載置し、さらにその上に化粧材を載
置し、熱圧成形して得られる化粧板の表面平滑性がさら
に良好なものとなる。さらに、熱圧成形時における硬化
性組成物の流動性がより良好であるため、熱圧時の圧力
をより低く設定できるという利点も生じる。一方、これ
らを混合する手段も特に限定されるものでなく例えば、
ブレンダー、ニーダー、ミキシングロール、バンバリー
ミキサーなどの混練機、あるいは、単軸、二軸押出機を
用いて行うことができる。混練のためミキシングロール
を用いたときには、混練と同時にシート化が行え効率的
である。さらに単軸、二軸押出機にTダイを取り付けT
ダイに設けられたスリットを介して押し出すことによっ
ても混練と同時にシート化が行え効率的である。また、
混練とシート化を同時に行わず、混練の後、シート化を
二次的に行う場合には、混練された硬化性組成物をカレ
ンダー製膜装置、ミキシングロール等に供給することに
よりこれを行う。なおシート化する際の温度についてで
あるが、熱可塑性樹脂が軟化して均一に分散でき、しか
も熱硬化性樹脂の架橋反応が進行しない温度範囲に設定
することが望ましい。In the present invention, as a more preferred embodiment, a sheet-shaped curable composition comprising a chemically modified wood material, a thermosetting resin, a polymerization initiator, and a thermoplastic resin is used. By thus adding the thermoplastic resin, the kneading of the curable composition becomes very effective, and the thickness of the sheet can be adjusted relatively easily. The uniformity of is good. Therefore, the sheet-like curable composition is placed on the wooden base material, the decorative material is further placed on it, and the surface smoothness of the decorative sheet obtained by thermocompression molding is further improved. . Further, since the fluidity of the curable composition at the time of hot pressing is better, there is an advantage that the pressure at hot pressing can be set lower. On the other hand, the means for mixing these is not particularly limited, for example,
It can be carried out using a kneader such as a blender, a kneader, a mixing roll, a Banbury mixer, or a single-screw or twin-screw extruder. When a mixing roll is used for kneading, it is efficient because it can be formed into a sheet simultaneously with kneading. Furthermore, attach a T die to a single-screw or twin-screw extruder.
By extruding through a slit provided in the die, kneading and sheet formation can be performed efficiently. Also,
When the kneading and the sheeting are not simultaneously performed and the kneading and the sheeting are secondarily performed after the kneading, the kneading curable composition is supplied to a calender film forming apparatus, a mixing roll or the like. Regarding the temperature at the time of forming into a sheet, it is desirable to set it in a temperature range in which the thermoplastic resin is softened and can be uniformly dispersed, and the crosslinking reaction of the thermosetting resin does not proceed.
【0017】次に、このようにして得られる硬化性組成
物を木質基材に載置する。そして、さらにその上に未硬
化状態の熱硬化性樹脂が浸透、透過しうる化粧材を載置
する。次いで所要時間、熱圧成形することにより、木質
基材と化粧材とを一体化させるとともに、主として硬化
性組成物中の熱硬化性樹脂を化粧材に浸透、さらにその
反対の面にまでしみ出させ、硬化せしめる。なお当然の
ことながら、ここにおいて化粧材、硬化性組成物、木質
基材の順番に載置を行ってもいっこうに構わない。Next, the curable composition thus obtained is placed on a wood base material. Then, a decorative material through which the uncured thermosetting resin can permeate and permeate is placed thereon. Then, by thermocompression molding for a required time, the wooden base material and the decorative material are integrated, and at the same time, the thermosetting resin in the curable composition penetrates into the decorative material and exudes to the opposite surface. Let it cure. Of course, it does not matter if the decorative material, the curable composition, and the wood base material are placed in this order.
【0018】さらに、熱圧成形の際、木質基材が圧密化
するほどの圧力をかけてもかまわない。こうすることに
よって、木質基材の硬度、強度が向上する。なお、熱圧
成形の際、シート状の硬化性組成物の表面に平滑な鏡面
板をあてがってから熱圧成形すれば、得られる化粧板の
表面がより平滑となり、美観的に好ましい。また、同じ
く熱圧成形の際、シート状の硬化性組成物の表面にエン
ボス模様が施された板をあてがってから熱圧成形すれ
ば、エンボス模様が、得られる化粧板の表面に転写さ
れ、意匠性のあるものとなる。Furthermore, during thermocompression molding, a pressure may be applied to the wood base material so as to consolidate it. By doing so, the hardness and strength of the wooden base material are improved. In the thermocompression molding, if a smooth mirror plate is applied to the surface of the sheet-shaped curable composition and then the thermocompression molding is performed, the surface of the obtained decorative plate becomes smoother, which is aesthetically preferable. In the same manner, in the thermocompression molding, if a sheet having an embossed pattern on the surface of the sheet-shaped curable composition is applied and then thermocompression molded, the embossed pattern is transferred to the surface of the obtained decorative board, It becomes a design thing.
【0019】なお、硬化性組成物の載置量は木質基材の
材質、厚さ、表面状態または、化粧材の材質、厚さおよ
び製造しようとする化粧板の外観などによって異なる。
化粧板が平滑な化粧を得ようとする場合には硬化性組成
物の積層量は0.05kg/m2から1.0kg/m2 で十分で
あり、エンボス模様を施す場合には1.0kg/m2 以上の
硬化性組成物を積層させることが好ましい。また、厚み
の薄い木質基材を用いた時などにおいて見られる硬化性
組成物の硬化収縮応力に起因するソリの問題を解消する
ため、木質基材の裏面に、本発明において使用する硬化
性組成物、熱硬化性樹脂の液体を噴霧塗布した木粉、あ
るいは、熱硬化性樹脂含浸紙などを位置させて熱圧する
ようにしてもよい。このようにすることにより化粧板の
ソリを防ぐことができる。The amount of the curable composition to be placed differs depending on the material and thickness of the wood base material, the surface condition, the material and thickness of the decorative material, the appearance of the decorative plate to be manufactured, and the like.
The amount of lamination of the curable composition when the veneer is to be obtained a smooth makeup is sufficient from 0.05 kg / m 2 at 1.0kg / m 2, when subjected to the embossed pattern is 1.0kg It is preferable to laminate a curable composition of / m 2 or more. Further, in order to solve the problem of warping due to the curing shrinkage stress of the curable composition that is seen when using a thin wood base material, the curable composition used in the present invention on the back surface of the wood base material. An object, a wood powder spray-coated with a liquid of a thermosetting resin, or a thermosetting resin-impregnated paper may be positioned and heated. By doing so, warping of the decorative plate can be prevented.
【0020】加熱加圧条件は化粧板の種類、重合開始剤
の種類、熱硬化性樹脂の種類、化学修飾木質材の種類に
よって適宜設定されるが、一般的には 加熱温度は10
0〜200℃の範囲が適当である。また圧力は化学修飾
木質材成分がその温度で可塑化するのに必要な圧力でよ
く、一般的には10〜200kg/cm2であり、好ましくは
20〜50kg/cm2である。加圧時間は1〜20分程度で
よい。これらの熱圧条件下で、該シート状の硬化性組成
物の可塑化と架橋が行われるとともに、該シート状の硬
化性組成物の一部が該木質基材に含浸され、硬化するこ
とによって該木質基材が強化される。The heating and pressurizing conditions are appropriately set depending on the type of decorative board, the type of polymerization initiator, the type of thermosetting resin, and the type of chemically modified wood material. Generally, the heating temperature is 10
A range of 0 to 200 ° C is suitable. The pressure may be the pressure required for the chemically modified wood material component to plasticize at that temperature, generally 10 to 200 kg / cm 2 , and preferably 20 to 50 kg / cm 2 . The pressing time may be about 1 to 20 minutes. Under these hot-pressing conditions, the sheet-shaped curable composition is plasticized and crosslinked, and a part of the sheet-shaped curable composition is impregnated into the wood base material and cured. The wood substrate is reinforced.
【0021】また、化学修飾木質材としてオリゴエステ
ル化木質材を使用する場合においては、オリゴエステル
化木質材の製造段階において熱可塑性樹脂を添加混合す
ることが望ましい。このようにすることによって硬化性
組成物中の各成分がさらに一層均一に分散するので、最
終的な化粧面のむらをより少なくすることができる。When an oligoesterified wood material is used as the chemically modified wood material, it is desirable to add and mix a thermoplastic resin at the production stage of the oligoesterified wood material. By doing so, the respective components in the curable composition are evenly dispersed, so that the unevenness of the final cosmetic surface can be further reduced.
【0022】また、本発明においては、熱硬化性樹脂の
配合量が、化学修飾木質材100重量部に対して1〜6
0重量部であることが望ましい。熱硬化性樹脂の配合量
をこの範囲に設定することにより得られる化粧板の表面
硬度、耐摩耗性が良好なものとなり、さらに、熱圧成形
時、粘度低下を起こした熱硬化性樹脂が木質基材の側面
から外部に流出することがなく好ましい。また、化学修
飾木質材との親和性が良好であるという理由により、熱
硬化性樹脂として、不飽和ポリエステル樹脂を上記配合
量用いることがさらに好ましい。Further, in the present invention, the blending amount of the thermosetting resin is 1 to 6 with respect to 100 parts by weight of the chemically modified wood material.
It is preferably 0 parts by weight. By setting the blending amount of the thermosetting resin in this range, the surface hardness and wear resistance of the decorative board obtained will be good, and the thermosetting resin whose viscosity has decreased during thermocompression molding is wood-based. It is preferable because it does not flow out from the side surface of the base material. Further, it is more preferable to use an unsaturated polyester resin as the thermosetting resin in the above blending amount because it has a good affinity with the chemically modified wood material.
【0023】[0023]
【作用】本発明の特徴は、化学修飾木質材、熱硬化性樹
脂および重合開始剤から成る硬化性組成物を木質基材上
に載置し、さらにその上に未硬化状態の熱硬化性樹脂が
浸透、透過しうる化粧材を載置して、熱圧することにあ
る。このようにすることにより、主として該硬化性組成
物中の熱硬化性樹脂が化粧材に浸透し、さらに、その反
対面にまでしみ出して硬化する。このため木質基材と化
粧材が、熱硬化性樹脂、および化学修飾木質材によって
強固に一体化される。この結果、従来問題となってい
た、接着不良によって浮き現象を生じるという問題が解
消される。またこのようにして得られる化粧板は優れた
美観を有し、しかも表面平滑性、表面硬度、耐摩耗性お
よび耐浸せき剥離性に優れた表面を与える。A feature of the present invention is that a curable composition comprising a chemically modified wood material, a thermosetting resin and a polymerization initiator is placed on a wood base material, and further, an uncured thermosetting resin is placed thereon. It is to place a cosmetic material that can penetrate and permeate and heat it. By doing so, the thermosetting resin in the curable composition mainly permeates the decorative material, and further exudes to the opposite surface to be cured. Therefore, the wood base material and the decorative material are firmly integrated by the thermosetting resin and the chemically modified wood material. As a result, the problem that a floating phenomenon occurs due to defective adhesion, which has been a problem in the past, is solved. In addition, the decorative sheet thus obtained has an excellent appearance and gives a surface excellent in surface smoothness, surface hardness, abrasion resistance and dipping resistance.
【0024】また、この方法によれば、表面が平滑でな
い木質基材を用いても、あるいは、化粧板の表面に硬化
処理を施さなくても、表面に平滑で透明な被膜層を形成
できる。そして該化粧板は、化粧材が有する木目などの
模様が、被膜層を通して非常に鮮明に現出され、美しい
外観を呈する。Further, according to this method, a smooth and transparent coating layer can be formed on the surface of a decorative board without using a wood base material having a non-smooth surface or without applying a hardening treatment to the surface of the decorative board. Then, the decorative board has a beautiful appearance in which the pattern such as wood grain of the decorative material is very clearly revealed through the coating layer.
【0025】さらに、硬化性組成物中に化学修飾木質材
が含まれることによって、熱圧工程において、熱硬化性
樹脂の架橋による硬化が始まる前に、熱硬化性樹脂の急
激な粘度低下が起こり、該熱硬化性樹脂が木質基材の側
面から外部に流出するという問題点が解消される。加え
て、熱圧時、化粧材に浸透、透過する硬化性組成物中の
熱硬化性樹脂を適度な量に保つことができるという利点
をもたらす。これは熱圧成型工程時、熱硬化性樹脂が急
激な粘度低下を起こす時点において化学修飾木質材は、
まだ十分な可塑化状態にはなく、依然、粉体の性質を残
しているため、粘度低下した熱硬化性樹脂を吸収し、流
出を防止する作用をするためと考えられる。Further, the chemically modified wood material contained in the curable composition causes a rapid decrease in viscosity of the thermosetting resin before the curing by the crosslinking of the thermosetting resin starts in the hot pressing step. The problem that the thermosetting resin flows out from the side surface of the wooden base material is solved. In addition, there is an advantage that the thermosetting resin in the curable composition that permeates and permeates into the cosmetic material during hot pressing can be maintained in an appropriate amount. This is because when the thermosetting resin undergoes a rapid decrease in viscosity during the thermocompression molding process, the chemically modified wood material
Since it is not yet in a sufficiently plasticized state and still retains the properties of powder, it is considered that it absorbs the thermosetting resin whose viscosity has been lowered and acts to prevent outflow.
【0026】[0026]
・不飽和ポリエステル((株)日本触媒製、「N−34
0HV」) 〔重合開始剤〕 ・ジクミルパーオキサイド(化薬アクゾ(株)製、「三
井DCP」、1分間での半減期温度:179℃) 〔熱可塑性樹脂〕 ・エチレン−酢酸ビニル共重合体(住友化学工業(株)
製、「スミテートKA−3」、酢酸ビニル含量:28w
t%、ビカット軟化点:39℃) ・エチレン−エチルアクリレート−無水マレイン酸共重
合体(住友シーディエフ(株)製、「ボンダインTX8
030」、ビカット軟化点:68℃) 一方、以下の実施例、比較例で示す物性値の測定は次の
規格に準拠した。 ・引きかき硬度試験B試験 :JAS特殊合板 ・1類浸せきはくり試験 :JAS特殊合板 ・耐摩耗性試験 :JIS A1453(総回転数1000回) ・耐衝撃性試験 :JIS A5908・ Unsaturated polyester (N-34 manufactured by Nippon Shokubai Co., Ltd.)
0HV ") [Polymerization initiator] -Dicumyl peroxide (manufactured by Kayaku Akzo Co., Ltd.," Mitsui DCP ", half-life temperature in 1 minute: 179 ° C) [Thermoplastic resin] -Ethylene-vinyl acetate copolymer Combined (Sumitomo Chemical Co., Ltd.)
Made, "Smitate KA-3", vinyl acetate content: 28w
t%, Vicat softening point: 39 ° C) -Ethylene-ethyl acrylate-maleic anhydride copolymer (manufactured by Sumitomo CDF, "Bondaine TX8"
030 ", Vicat softening point: 68 ° C) Meanwhile, the measurement of physical properties shown in the following Examples and Comparative Examples complied with the following standards.・ Scratch hardness test B test: JAS special plywood ・ Type 1 immersion peeling test: JAS special plywood ・ Abrasion resistance test: JIS A1453 (total number of revolutions 1000 times) ・ Impact resistance test: JIS A5908
【0027】[実施例1]乾燥木粉(商品名:LIGNOCEL
S-150TR;J.Rettenmaier & Sohne社製)750g、無
水マレイン酸100g、およびエチレン−酢酸ビニル共
重合体50gを加圧型ニーダーに充填して、115℃で
1時間撹拌下に反応せしめた。その後、アリルグリシジ
ルエーテル(ダイソー(株)製、「ネオアリルG」)1
50gを添加し、さらに、115℃で1時間撹拌下に反
応せしめた。次に、得られたオリゴエステル化木質材と
エチレン−酢酸ビニル共重合体混合物300g、不飽和
ポリエステル樹脂120g、およびジクミルパーオキサ
イド9gをミキシングロールにより均一になるまで混合
し、次いで該混合物を厚さ0.4mm、幅30cmのシ
ート状で取り出すことによって、シート状の硬化性組成
物を得た。なお、ミキシングロールによる混合にあたっ
ては意図的な加温は行わなかった。次に、普通化粧紙
(30g/m2 )を鏡面板上に置き、その上に該シート
状の硬化性組成物を載置し、さらにその上に大きさ30
cm×30cm×1.5cmのパーティクルボードを載
置し、プレス機の熱板間に挿入して、温度150℃、圧
力20kgf/cm2 の熱圧条件で5分間熱圧成形を行
った。このようにして得られた化粧板は表面が強靭で硬
く、緻密性を有し、光沢のあるプラスチック様の優れた
美観を有するものであった。さらに、この化粧板の硬
度、耐浸せきはくり性、耐摩耗性、耐衝撃性を評価し
た。その結果を表1に示す。[Example 1] Dry wood powder (trade name: LIGNOCEL
S-150TR; manufactured by J. Rettenmaier & Sohne) 750 g, maleic anhydride 100 g, and ethylene-vinyl acetate copolymer 50 g were charged in a pressure type kneader and reacted at 115 ° C. for 1 hour with stirring. Then, allyl glycidyl ether (manufactured by Daiso Co., Ltd., "Neoallyl G") 1
50 g was added, and the mixture was further reacted at 115 ° C. for 1 hour with stirring. Next, 300 g of the obtained oligoesterified wood material, ethylene-vinyl acetate copolymer mixture, 120 g of unsaturated polyester resin, and 9 g of dicumyl peroxide were mixed with a mixing roll until uniform, and then the mixture was thickened. A sheet-shaped curable composition was obtained by taking out a sheet having a size of 0.4 mm and a width of 30 cm. Note that no intentional heating was performed during mixing with the mixing roll. Next, ordinary decorative paper (30 g / m 2 ) is placed on a mirror plate, the curable composition in sheet form is placed thereon, and the size 30
A cm × 30 cm × 1.5 cm particle board was placed and inserted between the hot plates of the press machine, and thermocompression molding was performed for 5 minutes under the heat and pressure conditions of a temperature of 150 ° C. and a pressure of 20 kgf / cm 2 . The surface of the decorative board thus obtained was tough, hard, dense, and had an excellent aesthetic appearance like a glossy plastic. Further, the hardness, dipping resistance, abrasion resistance, and impact resistance of this decorative plate were evaluated. Table 1 shows the results.
【0028】[実施例2]パーティクルボードの乾燥サ
ンダー粉(含水率:0.5%、80メッシュ篩を通過し
たもの)750g、無水マレイン酸100g、およびエ
チレン−酢酸ビニル共重合体50gを加圧型ニーダーに
充填して、115℃で1時間撹拌下に反応せしめた。そ
の後、アリルグリシジルエーテル(ダイソー(株)製、
「ネオアリルG」)150gを添加し、さらに、115
℃で1時間撹拌下に反応せしめた。次に、得られたオリ
ゴエステル化木質材とエチレン−酢酸ビニル共重合体の
混合物300g、不飽和ポリエステル樹脂100g、お
よびジクミルパーオキサイド7.5gをミキシングロー
ルにより均一になるまで混合し、次いで該混合物を厚さ
0.4mm、幅30cmのシート状で取り出すことによ
って、シート状の硬化性組成物を得た。なお、ミキシン
グロールによる混合にあたっては意図的な加温は行わな
かった。次に、普通化粧紙(30g/m2 )を鏡面板上
に置き、その上に該シート状の硬化性組成物を載置し、
さらにその上に大きさ30cm×30cm×1.5cm
のパーティクルボードを載置し、プレス機の熱板間に挿
入して、温度150℃、圧力20kgf/cm2 の熱圧
条件で5分間熱圧成形を行った。このようにして得られ
た化粧板は表面が強靭で硬く、緻密性を有し、光沢のあ
るプラスチック様の優れた美観を有するものであった。
さらに、この化粧板の硬度、耐浸せきはくり性、耐摩耗
性、耐衝撃性を評価した。その結果を表1に示す。[Example 2] 750 g of dried sander powder of particle board (water content: 0.5%, which passed through 80 mesh sieve), 100 g of maleic anhydride, and 50 g of ethylene-vinyl acetate copolymer were pressurized. The mixture was charged in a kneader and reacted at 115 ° C. for 1 hour with stirring. After that, allyl glycidyl ether (manufactured by Daiso Co., Ltd.,
"Neoallyl G") 150 g, and then 115
The mixture was reacted at 0 ° C. for 1 hour with stirring. Next, 300 g of the mixture of the obtained oligoesterified wood material and ethylene-vinyl acetate copolymer, 100 g of the unsaturated polyester resin, and 7.5 g of dicumyl peroxide were mixed with a mixing roll until uniform, and then the mixture was mixed. A sheet-shaped curable composition was obtained by removing the mixture into a sheet having a thickness of 0.4 mm and a width of 30 cm. Note that no intentional heating was performed during mixing with the mixing roll. Next, ordinary decorative paper (30 g / m 2 ) is placed on the mirror surface plate, and the curable composition in sheet form is placed thereon,
Furthermore, the size is 30 cm x 30 cm x 1.5 cm.
The particle board of No. 2 was placed and inserted between the hot plates of the press machine, and thermocompression molding was carried out for 5 minutes under the conditions of a temperature of 150 ° C. and a pressure of 20 kgf / cm 2 . The surface of the decorative board thus obtained was tough, hard, dense, and had an excellent aesthetic appearance like a glossy plastic.
Further, the hardness, dipping resistance, abrasion resistance, and impact resistance of this decorative plate were evaluated. Table 1 shows the results.
【0029】[実施例3]乾燥木粉(含水率:0.7
%、商品名:LIGNOCEL S-150TR ;J.Rettenmaier &Sohne
社製;繊維長:30〜60μ)750g、無水マレイ
ン酸100g、およびエチレン−エチルアクリレート−
無水マレイン酸共重合体100gを加圧型ニーダーに充
填して、115℃で1時間撹拌下に反応せしめた。その
後、アリルグリシジルエーテル(ダイソー(株)製、
「ネオアリルG」)150gを添加し、さらに、115
℃で1時間撹拌下に反応せしめた。次に、得られたオリ
ゴエステル化木質材とエチレン−エチルアクリレート−
無水マレイン酸共重合体の反応物300g、不飽和ポリ
エステル樹脂100g、およびジクミルパーオキサイド
7.5gをミキシングロールにより均一になるまで混合
し、次いで該混合物を厚さ0.4mm、幅30cmのシ
ート状で取り出すことによって、シート状の硬化性組成
物を得た。なお、ミキシングロールによる混合にあたっ
ては意図的な加温は行わなかった。次に、普通化粧紙
(30g/m2 )を鏡面板上に置き、その上に該シート
状の硬化性組成物を載置し、さらにその上に大きさ30
cm×30cm×1.5cmのパーティクルボードを載
置し、プレス機の熱板間に挿入して、温度150℃、圧
力20kgf/cm2 の熱圧条件で5分間熱圧成形を行
った。このようにして得られた化粧板は表面が強靭で硬
く、緻密性を有し、光沢のあるプラスチック様の優れた
美観を有するものであった。さらに、この得られた化粧
板の硬度、耐浸せきはくり性、耐摩耗性、耐衝撃性を評
価した。その結果を表1に示す。 [実施例4][Example 3] Dry wood powder (water content: 0.7
%, Product name: LIGNOCEL S-150TR; J.Rettenmaier & Sohne
KK; Fiber length: 30-60 μ) 750 g, maleic anhydride 100 g, and ethylene-ethyl acrylate-
A maleic anhydride copolymer (100 g) was charged into a pressure type kneader and reacted at 115 ° C. for 1 hour with stirring. After that, allyl glycidyl ether (manufactured by Daiso Co., Ltd.,
"Neoallyl G") 150 g, and then 115
The mixture was reacted at 0 ° C. for 1 hour with stirring. Next, the obtained oligoesterified wood material and ethylene-ethyl acrylate-
300 g of a maleic anhydride copolymer reaction product, 100 g of an unsaturated polyester resin, and 7.5 g of dicumyl peroxide were mixed with a mixing roll until uniform, and then the mixture was formed into a sheet having a thickness of 0.4 mm and a width of 30 cm. The sheet-shaped curable composition was obtained by taking out the curable composition. Note that no intentional heating was performed during mixing with the mixing roll. Next, ordinary decorative paper (30 g / m 2 ) is placed on a mirror plate, the curable composition in sheet form is placed thereon, and the size 30
A cm × 30 cm × 1.5 cm particle board was placed and inserted between the hot plates of the press machine, and thermocompression molding was performed for 5 minutes under the heat and pressure conditions of temperature 150 ° C. and pressure 20 kgf / cm 2 . The surface of the decorative board thus obtained was tough, hard, dense, and had an excellent aesthetic appearance like a glossy plastic. Further, the hardness, dipping resistance, abrasion resistance, and impact resistance of the obtained decorative board were evaluated. Table 1 shows the results. [Example 4]
【0030】セルロースアセテート(含水率:0.5
%、商品名:L−AC、DS2.4、ダイセル化学工業
(株))700g、フタル酸ジメチル300g、および
エチレン−酢酸ビニル共重合体50gを加圧型ニーダー
に充填して、115℃で1時間撹拌せしめた。次に、得
られたセルロースアセテートとフタル酸ジメチルとエチ
レン−酢酸ビニル共重合体の混合物300g、不飽和ポ
リエステル樹脂120g、およびジクミルパーオキサイ
ド9gをミキシングロールにより均一になるまで混合
し、次いで該混合物を厚さ0.4mm、幅30cmのシ
ート状で取り出すことによって、シート状の硬化性組成
物を得た。なお、ミキシングロールによる混合にあたっ
ては意図的な加温は行わなかった。次に、普通化粧紙
(30g/m2 )を鏡面板上に置き、その上に該シート
状の硬化性組成物を載置し、さらにその上に大きさ30
cm×30cm×1.5cmのパーティクルボードを載
置し、プレス機の熱板間に挿入して、温度150℃、圧
力20kgf/cm2 の熱圧条件で5分間熱圧成形を行
った。このようにして得られた化粧板は表面が強靭で硬
く、緻密性を有し、光沢のあるプラスチック様の優れた
美観を有するものであった。さらに、この化粧板の硬
度、耐浸せきはくり性、耐摩耗性、耐衝撃性を評価し
た。その結果を表1に示す。 [比較例1]Cellulose acetate (water content: 0.5
%, Trade name: L-AC, DS2.4, Daicel Chemical Industries Ltd. 700 g, dimethyl phthalate 300 g, and ethylene-vinyl acetate copolymer 50 g were charged in a pressure type kneader, and at 115 ° C. for 1 hour. Stirred. Next, 300 g of the obtained mixture of cellulose acetate, dimethyl phthalate and ethylene-vinyl acetate copolymer, 120 g of unsaturated polyester resin, and 9 g of dicumyl peroxide were mixed with a mixing roll until uniform, and then the mixture was mixed. Was taken out as a sheet having a thickness of 0.4 mm and a width of 30 cm to obtain a sheet-shaped curable composition. Note that no intentional heating was performed during mixing with the mixing roll. Next, ordinary decorative paper (30 g / m 2 ) is placed on a mirror plate, the curable composition in sheet form is placed thereon, and the size 30
A cm × 30 cm × 1.5 cm particle board was placed and inserted between the hot plates of the press machine, and thermocompression molding was performed for 5 minutes under the heat and pressure conditions of temperature 150 ° C. and pressure 20 kgf / cm 2 . The surface of the decorative board thus obtained was tough, hard, dense, and had an excellent aesthetic appearance like a glossy plastic. Further, the hardness, dipping resistance, abrasion resistance, and impact resistance of this decorative plate were evaluated. Table 1 shows the results. [Comparative Example 1]
【0031】乾燥木粉(含水率:0.7%、商品名:LI
GNOCEL S-150TR;J.Rettenmaier & Sohne社製;繊維長:
30〜60μ)300gとエチレン−酢酸ビニル共重合
体20gを加圧型ニーダーに充填して、不飽和ポリエス
テル樹脂120g、およびジクミルパーオキサイド9g
をミキシングロールに添加混合したが、乾燥木粉と不飽
和ポリエステル樹脂とのなじみが悪く粉体状の硬化性組
成物しか得られなかった。次に、普通化粧紙(30g/
m2 )を鏡面板上に置き、その上に該硬化性組成物を散
布(フォーミング)して、さらにその上に大きさ30c
m×30cm×1.5cmのパーティクルボードを載置
し、プレス機の熱板間に挿入して、温度150℃、圧力
20kgf/cm2 の熱圧条件で5分間熱圧成形を行っ
た。このようにして得られた化粧板は表面平滑性がな
く、光沢のないものであった。さらに、この化粧板の硬
度、耐浸せきはくり性、耐摩耗性、耐衝撃性を評価し
た。その結果を表1に示す。Dry wood flour (water content: 0.7%, trade name: LI
GNOCEL S-150TR; made by J. Rettenmaier &Sohne; fiber length:
30-60 μ) 300 g and ethylene-vinyl acetate copolymer 20 g were charged in a pressure type kneader to give unsaturated polyester resin 120 g and dicumyl peroxide 9 g.
Was mixed into a mixing roll, but the dry wood powder and the unsaturated polyester resin were poorly compatible with each other and only a powdery curable composition was obtained. Next, plain decorative paper (30 g /
m 2 ) is placed on a mirror surface plate, the curable composition is sprinkled (forming) thereon, and a size of 30 c is further applied.
A m × 30 cm × 1.5 cm particle board was placed and inserted between the hot plates of the press machine, and thermocompression molding was performed for 5 minutes under the heat and pressure conditions of temperature 150 ° C. and pressure 20 kgf / cm 2 . The decorative board thus obtained had no surface smoothness and was not glossy. Further, the hardness, dipping resistance, abrasion resistance, and impact resistance of this decorative plate were evaluated. Table 1 shows the results.
【0032】[比較例2]30cm×30cm×1.5
cmのパーティクルボード上に尿素樹脂を40g/m2
塗布し、その上に普通化粧紙(30g/m2 )を載置
し、プレス機の熱板間に挿入して、温度130℃、圧力
20kgf/cm2 熱圧条件で20秒間熱圧成形を行
い、化粧板を得た。このようにして得られた化粧板の硬
度、耐浸せきはくり性、耐摩耗性、耐衝撃性を評価し
た。その結果を表1に示す。[Comparative Example 2] 30 cm × 30 cm × 1.5
40g / m 2 of urea resin on cm particle board
After coating, put ordinary decorative paper (30 g / m 2 ) on it, insert it between the hot plates of the press machine, and heat-press molding for 20 seconds at a temperature of 130 ° C. and a pressure of 20 kgf / cm 2 hot-pressing. Then, a decorative board was obtained. The hardness, dipping resistance, abrasion resistance, and impact resistance of the thus obtained decorative sheet were evaluated. Table 1 shows the results.
【0033】表1より明らかなように、本発明によって
得られる化粧板は十分な表面硬度、耐浸せきはくり性、
耐摩耗性、耐衝撃性を有している。As is apparent from Table 1, the decorative board obtained by the present invention has sufficient surface hardness, dipping resistance and peeling resistance,
It has abrasion resistance and impact resistance.
【0034】[0034]
【表1】 [Table 1]
【0035】[0035]
【発明の効果】以上説明したように本発明によれば、優
れた美観を有し、かつ表面硬度や耐摩耗性および耐水性
などに優れた化粧板を工業的に有利に製造する方法が提
供される。この製造方法によって得られる化粧板は、表
面が平滑で、優れた美観を有し、かつ表面硬度、耐摩耗
性および耐水性等に優れている。また、本製造方法は木
質基材を選ばず、例えば表面の軟かい樹木、木目柄の不
鮮明な樹木からも優れた美観を有する化粧板を製造する
ことができる。このように本発明は建材分野において好
適に使用される化粧板の製造方法を提供するものであ
る。INDUSTRIAL APPLICABILITY As described above, according to the present invention, there is provided a method for industrially producing a decorative board having an excellent aesthetic appearance and excellent surface hardness, abrasion resistance and water resistance. To be done. The decorative board obtained by this manufacturing method has a smooth surface, has an excellent aesthetic appearance, and is excellent in surface hardness, abrasion resistance, water resistance and the like. In addition, the present production method can produce a decorative board having an excellent aesthetic appearance even from a tree having a soft surface or a tree having a poor grain pattern, regardless of a wooden base material. Thus, the present invention provides a method for manufacturing a decorative board that is preferably used in the field of building materials.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 松田 ▲ひで▼明 香川県丸亀市中津町1515番地 大倉工業株 式会社内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Matsuda ▲ Hide ▼ Akira 1515 Nakatsu-cho, Marugame-shi, Kagawa Inside Okura Industrial Co., Ltd.
Claims (9)
合開始剤から成る硬化性組成物を木質基材上に載置し、
さらにその上に未硬化状態の熱硬化性樹脂が浸透、透過
しうる化粧材を載置して、熱圧することを特徴とする化
粧板の製造方法。1. A curable composition comprising a chemically modified wood material, a thermosetting resin and a polymerization initiator is placed on a wood base material,
A method of manufacturing a decorative board, further comprising placing a decorative material on which an uncured thermosetting resin can penetrate and permeate and heat-pressing it.
性樹脂および重合開始剤から成るシート状の硬化性組成
物を木質基材に載置し、さらにその上に未硬化状態の熱
硬化性樹脂が浸透、透過しうる化粧材を載置して、熱圧
することを特徴とする化粧板の製造方法。2. A sheet-like curable composition comprising a chemically modified wood material, a thermoplastic resin, a thermosetting resin and a polymerization initiator is placed on a wood base material, and further uncured thermosetting is placed thereon. A method for manufacturing a decorative plate, comprising placing a decorative material that allows the resin to permeate and permeate and applying heat.
しうる化粧材が普通化粧紙、あるいは、化粧単板である
ことを特徴とする請求項1乃至2に記載の化粧板の製造
方法。3. The production of a decorative board according to claim 1, wherein the decorative material through which the uncured thermosetting resin can permeate and permeate is a plain decorative paper or a decorative veneer. Method.
重量部に対して1〜20重量部添加混合されたことを特
徴とする請求項2乃至3のいずれかに記載の化粧板の製
造方法。4. The thermoplastic resin is a chemically modified wood material 100.
The method for producing a decorative board according to any one of claims 2 to 3, wherein 1 to 20 parts by weight is added and mixed with respect to parts by weight.
共重合体であることを特徴とする請求項2乃至4のいず
れかに記載の化粧板の製造方法。5. The method for producing a decorative board according to claim 2, wherein the thermoplastic resin is an ethylene-vinyl acetate copolymer.
重量部に対して1〜60重量部添加混合されたことを特
徴とする請求項1乃至5のいずれかに記載の化粧板の製
造方法。6. The thermosetting resin is a chemically modified wood material 100.
The method for producing a decorative board according to any one of claims 1 to 5, wherein 1 to 60 parts by weight is added and mixed with respect to parts by weight.
脂であることを特徴とする請求項1乃至6のいずれかに
記載の化粧板の製造方法。7. The method for manufacturing a decorative board according to claim 1, wherein the thermosetting resin is an unsaturated polyester resin.
水物およびエポキシ化合物を反応させて得られるオリゴ
エステル化木質材であることを特徴とする請求項1乃至
7のいずれかに記載の化粧板の製造方法。8. The chemically modified wood material is an oligoesterified wood material obtained by reacting a wood material with a polybasic acid anhydride and an epoxy compound, according to any one of claims 1 to 7. Manufacturing method of the decorative board.
いて、熱可塑性樹脂を添加混合し、得られたオリゴエス
テル化木質材と熱可塑性樹脂との混合物に熱硬化性樹脂
および重合開始剤を添加混合し、シート化することによ
りシート状の硬化性組成物を得ることを特徴とする請求
項8に記載の化粧板の製造方法。9. A thermoplastic resin is added and mixed in the step of producing an oligoesterified wood material, and a thermosetting resin and a polymerization initiator are added and mixed to the obtained mixture of the oligoesterified wood material and the thermoplastic resin. Then, the sheet-like curable composition is obtained by forming a sheet into a sheet, and the method for producing a decorative board according to claim 8, wherein.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20192295A JP2718910B2 (en) | 1995-08-08 | 1995-08-08 | Manufacturing method of decorative board |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20192295A JP2718910B2 (en) | 1995-08-08 | 1995-08-08 | Manufacturing method of decorative board |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0948090A true JPH0948090A (en) | 1997-02-18 |
| JP2718910B2 JP2718910B2 (en) | 1998-02-25 |
Family
ID=16449025
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20192295A Expired - Fee Related JP2718910B2 (en) | 1995-08-08 | 1995-08-08 | Manufacturing method of decorative board |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2718910B2 (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007090755A (en) * | 2005-09-29 | 2007-04-12 | Dainippon Printing Co Ltd | Decorative plate and method for producing the same |
| WO2007091614A1 (en) * | 2006-02-07 | 2007-08-16 | Dai Nippon Printing Co., Ltd. | Flooring material |
| JP2007224688A (en) * | 2006-02-27 | 2007-09-06 | Dainippon Printing Co Ltd | Floor material |
| JP2007239445A (en) * | 2006-02-07 | 2007-09-20 | Dainippon Printing Co Ltd | Flooring |
| JP2007247386A (en) * | 2006-02-20 | 2007-09-27 | Dainippon Printing Co Ltd | Flooring |
| JP2010234716A (en) * | 2009-03-31 | 2010-10-21 | Victor Co Of Japan Ltd | Wooden molded article and manufacturing method therefor |
| JP2014139400A (en) * | 2007-11-19 | 2014-07-31 | Vaelinge Innovation Ab | Fiber-based panel having abrasion-resistant surface |
-
1995
- 1995-08-08 JP JP20192295A patent/JP2718910B2/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007090755A (en) * | 2005-09-29 | 2007-04-12 | Dainippon Printing Co Ltd | Decorative plate and method for producing the same |
| WO2007091614A1 (en) * | 2006-02-07 | 2007-08-16 | Dai Nippon Printing Co., Ltd. | Flooring material |
| JP2007239445A (en) * | 2006-02-07 | 2007-09-20 | Dainippon Printing Co Ltd | Flooring |
| JP2007247386A (en) * | 2006-02-20 | 2007-09-27 | Dainippon Printing Co Ltd | Flooring |
| JP2007224688A (en) * | 2006-02-27 | 2007-09-06 | Dainippon Printing Co Ltd | Floor material |
| JP2014139400A (en) * | 2007-11-19 | 2014-07-31 | Vaelinge Innovation Ab | Fiber-based panel having abrasion-resistant surface |
| JP2010234716A (en) * | 2009-03-31 | 2010-10-21 | Victor Co Of Japan Ltd | Wooden molded article and manufacturing method therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2718910B2 (en) | 1998-02-25 |
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