JPH04216044A - Manufacture of composite panel - Google Patents
Manufacture of composite panelInfo
- Publication number
- JPH04216044A JPH04216044A JP2410728A JP41072890A JPH04216044A JP H04216044 A JPH04216044 A JP H04216044A JP 2410728 A JP2410728 A JP 2410728A JP 41072890 A JP41072890 A JP 41072890A JP H04216044 A JPH04216044 A JP H04216044A
- Authority
- JP
- Japan
- Prior art keywords
- wood
- metal foil
- layers
- wooden
- fibers
- 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
- 239000002131 composite material Substances 0.000 title claims abstract description 34
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 239000002023 wood Substances 0.000 claims abstract description 67
- 229910052751 metal Inorganic materials 0.000 claims abstract description 40
- 239000002184 metal Substances 0.000 claims abstract description 40
- 239000011888 foil Substances 0.000 claims abstract description 33
- 239000000853 adhesive Substances 0.000 claims abstract description 31
- 230000001070 adhesive effect Effects 0.000 claims abstract description 31
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 14
- 238000001035 drying Methods 0.000 claims abstract description 8
- 238000010030 laminating Methods 0.000 claims abstract description 8
- 238000003825 pressing Methods 0.000 claims abstract description 8
- 229920002522 Wood fibre Polymers 0.000 claims description 74
- 239000002025 wood fiber Substances 0.000 claims description 71
- 238000000034 method Methods 0.000 claims description 19
- 230000002265 prevention Effects 0.000 claims description 4
- 239000000835 fiber Substances 0.000 abstract description 9
- 238000010438 heat treatment Methods 0.000 abstract description 6
- 230000009970 fire resistant effect Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 46
- 239000007788 liquid Substances 0.000 description 39
- 150000002484 inorganic compounds Chemical class 0.000 description 18
- 229910010272 inorganic material Inorganic materials 0.000 description 18
- 239000011148 porous material Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 210000004027 cell Anatomy 0.000 description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 239000011094 fiberboard Substances 0.000 description 9
- -1 CaB r2 Chemical compound 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000002699 waste material Substances 0.000 description 5
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000011093 chipboard Substances 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000004254 Ammonium phosphate Substances 0.000 description 3
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 3
- 235000019289 ammonium phosphates Nutrition 0.000 description 3
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Inorganic materials [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 3
- WAKZZMMCDILMEF-UHFFFAOYSA-H barium(2+);diphosphate Chemical compound [Ba+2].[Ba+2].[Ba+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O WAKZZMMCDILMEF-UHFFFAOYSA-H 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000013049 sediment Substances 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 239000010875 treated wood Substances 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-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
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 235000008577 Pinus radiata Nutrition 0.000 description 2
- 241000218621 Pinus radiata Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- JLDSOYXADOWAKB-UHFFFAOYSA-N aluminium nitrate Chemical compound [Al+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JLDSOYXADOWAKB-UHFFFAOYSA-N 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 2
- 229910001626 barium chloride Inorganic materials 0.000 description 2
- LYSTYSFIGYAXTG-UHFFFAOYSA-L barium(2+);hydrogen phosphate Chemical compound [Ba+2].OP([O-])([O-])=O LYSTYSFIGYAXTG-UHFFFAOYSA-L 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 235000011148 calcium chloride Nutrition 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000004079 fireproofing Methods 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 241000218645 Cedrus Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000218691 Cupressaceae Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- 229910003252 NaBO2 Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000219000 Populus Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-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
- PQLAYKMGZDUDLQ-UHFFFAOYSA-K aluminium bromide Chemical compound Br[Al](Br)Br PQLAYKMGZDUDLQ-UHFFFAOYSA-K 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- NKQIMNKPSDEDMO-UHFFFAOYSA-L barium bromide Chemical compound [Br-].[Br-].[Ba+2] NKQIMNKPSDEDMO-UHFFFAOYSA-L 0.000 description 1
- 229910001620 barium bromide Inorganic materials 0.000 description 1
- 150000001553 barium compounds Chemical class 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 238000007600 charging Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- QSDQMOYYLXMEPS-UHFFFAOYSA-N dialuminium Chemical compound [Al]#[Al] QSDQMOYYLXMEPS-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- 229910001623 magnesium bromide Inorganic materials 0.000 description 1
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Inorganic materials [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- NFMWFGXCDDYTEG-UHFFFAOYSA-N trimagnesium;diborate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]B([O-])[O-].[O-]B([O-])[O-] NFMWFGXCDDYTEG-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、防火性能に優れた建材
用又は家具用部材として用いられる複合板を効率的に製
造することのできる方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for efficiently producing a composite board having excellent fireproof performance and used as a building material or furniture member.
【0002】0002
【従来の技術】一般に挽材、合板、単板積層板(LVL
,LVB)と呼ばれる木質板は、適宜その表面に塗装、
紙張り等の加工を施した上で、建築用及び家具用部材と
して多種多様な用途に用いられている。[Prior art] Generally, sawn timber, plywood, veneer laminate (LVL)
, LVB) is coated on its surface as appropriate.
After being processed such as papering, it is used for a wide variety of purposes as construction and furniture components.
【0003】近年これら木質板に対する防火性能の向上
が要求されるようになり、この目的のために種々の提案
がなされている。例えば、木質単板と金属板とを積層複
合して複合板とする方法(特公昭53−39号公報)や
板又は単板状態で木材固有の細胞孔内に不燃性無機化合
物を分散定着することによって難燃化する方法(特開昭
61−244502号公報)等が知られている。[0003] In recent years, there has been a demand for improvements in the fireproof performance of these wood boards, and various proposals have been made for this purpose. For example, a method of laminating a wood veneer and a metal plate to make a composite board (Japanese Patent Publication No. 1983-39), or dispersing and fixing a nonflammable inorganic compound into the cell pores of wood in the form of a board or veneer. A method of making the material flame retardant (Japanese Unexamined Patent Publication No. 61-244502) is known.
【0004】0004
【発明が解決しようとする課題】しかしながら、これら
複合された木質板は一定の繊維方向を有するため、水分
の吸放出により膨張収縮が発生し、特に繊維方向に対し
て垂直の方向における膨張率が大きくなって寸法安定性
に欠け、更に表面塗装、紙張り等の加工の際に金属表面
に酸処理等の下地処理を施す必要がある等の問題点を有
していた。[Problems to be Solved by the Invention] However, since these composite wood boards have a fixed fiber direction, expansion and contraction occur due to absorption and release of moisture, and the expansion coefficient in the direction perpendicular to the fiber direction is particularly low. The metal surface becomes large and lacks dimensional stability, and furthermore, it is necessary to perform base treatment such as acid treatment on the metal surface when processing the surface, such as painting or papering.
【0005】また、木質板を板又は単板状態にて難燃化
する方法は、不燃性無機化合物を木材の絶乾重量に対し
て40%以上含浸分散させるためには、断面形状の大き
さ等にもよるが、不燃性無機化合物を溶解した溶液中に
木質板を長時間浸漬する必要があり、効率性が悪かった
。また、不燃性無機化合物は木質板の表裏面及び木口近
辺の周辺部に多く含浸され、長時間浸漬したとしても、
内部まで十分に且つ均一に分散定着させることは極めて
困難であった。不燃性無機化合物溶液中に浸漬処理した
後、木質板の外周部に付着した粉状の不燃性無機化合物
は水洗除去されるが、このようにして除去された不燃性
無機化合物を回収して再利用することが困難であるため
、不経済であると共に廃液の処理工程も必要となる、等
多くの問題点を有するものであった。[0005] In addition, in the method of making wood boards flame retardant in the form of a board or a veneer, in order to impregnate and disperse a nonflammable inorganic compound in an amount of 40% or more based on the absolute dry weight of the wood, the size of the cross-sectional shape must be adjusted. However, it was necessary to immerse the wooden board in a solution containing a nonflammable inorganic compound for a long time, which was inefficient. In addition, nonflammable inorganic compounds are impregnated in large quantities on the front and back surfaces of the wood board and in the peripheral area near the end of the wood board, so even if it is immersed for a long time,
It was extremely difficult to sufficiently and uniformly disperse and fix the particles inside. After being immersed in a nonflammable inorganic compound solution, the powdery nonflammable inorganic compounds that adhere to the outer periphery of the wood board are washed away with water. Since it is difficult to utilize, it is uneconomical and has many problems, such as requiring a waste liquid treatment process.
【0006】[0006]
【課題を解決するための手段】このような現状に鑑み、
本発明者は、防火性能に優れ且つ寸法安定性にも優れた
建築用板を提供すべく鋭意研究を重ねた結果、本発明を
完成するに至ったものである。[Means to solve the problem] In view of the current situation,
The present inventor has completed the present invention as a result of extensive research in order to provide a construction board with excellent fire protection performance and excellent dimensional stability.
【0007】即ち、本発明者は、廃材から得られる木質
繊維又は木削片を原料として一体成形する木質繊維板又
は木削片板の優れた寸法安定性に着目し、複数枚の木質
繊維板及び/又は木削片板と金属箔とを積層し複合化す
ることによって防火性能に優れた複合板を得ようと考え
、複数の木質繊維板/木削片板と金属箔とを交互に配し
接着剤を介して加熱圧締による接着を試みたが、加熱圧
締の途中で板材中の水分に起因するパンク現象が生じて
しまい、目的とする複合板を得ることができなかった。That is, the present inventor focused on the excellent dimensional stability of wood fiberboard or wood chip board that is integrally molded using wood fibers or wood chips obtained from waste wood, And/or with the idea of obtaining a composite board with excellent fire protection performance by laminating and compositing wood particle boards and metal foil, a plurality of wood fiberboards/wood particle boards and metal foil were arranged alternately. Attempts were made to bond the sheets by heat pressing using an adhesive, but a puncture caused by moisture in the board material occurred during heat pressing, and the desired composite board could not be obtained.
【0008】このパンク現象について木質繊維板を例に
して更に説明すると以下の通りである。まずチップを解
繊して得られた木質繊維に接着剤を塗布し乾燥した後、
この木質繊維を堆積してマット化したものを加熱成形し
て木質繊維板を得る。この木質繊維板について調湿を行
って大気中の水分を吸収させることにより平衡含水率に
至るまで養生された後、表面のサンディング加工及び定
寸への切断が行われる。この調湿養生は、加熱圧締によ
り得られた木質繊維板の含有水分両が非常に低く絶乾状
態に近くなっているため、そのままの状態でサンディン
グ加工及び切断加工を行うと、加工後に木質繊維板が水
分を吸収して膨張に伴う反りが発生してしまうため、こ
れを防ぐ目的で行われる。このように木質繊維板として
得られるものは平衡含水率まで水分を含有しているため
、このような木質繊維板を複数積層して接着剤を介して
加熱圧締すると、板材中の水分が蒸発して外に出ようと
する力が生じ、解圧の際に水蒸気の放出に伴うパンクが
発生してしまうことが判明した。この現象は木削片板を
用いた場合も同様である。This puncture phenomenon will be further explained below using a wood fiber board as an example. First, the wood fibers obtained by defibrating the chips are coated with adhesive, dried, and then
The wood fibers are piled up and made into a mat, which is then heated and molded to obtain a wood fiberboard. After the wood fiberboard is cured to an equilibrium moisture content by controlling the humidity and absorbing moisture from the atmosphere, the surface is sanded and cut to size. With this humidity control curing, the moisture content of the wood fiberboard obtained by heat pressing is very low and it is close to an absolutely dry state, so if sanding and cutting are performed in that state, the wood will become This is done to prevent the fiberboard from absorbing moisture and causing warping due to expansion. Wood fiberboards obtained in this way contain water up to the equilibrium moisture content, so when multiple wood fiberboards are laminated and heat pressed together with an adhesive, the water in the wood fiberboards evaporates. It was discovered that a force was generated that tried to escape from the tank, causing punctures due to the release of water vapor during depressurization. This phenomenon is the same when a wood chip board is used.
【0009】そこで本発明者は、木質繊維板/木削片板
に代えて、木質繊維/木削片に熱硬化性樹脂接着剤を添
加し乾燥したものをコンベア上に落下堆積して得られる
木質堆積層と金属箔層とを交互に積層した後に加熱圧締
して接着一体成形することに想到し、本発明に至ったも
のである。[0009] Therefore, the inventor of the present invention proposed that instead of the wood fiber board/wood chip board, a thermosetting resin adhesive was added to the wood fiber/wood chip board, and the dried material was dropped and deposited on a conveyor. The present invention was developed based on the idea of alternately laminating wood deposit layers and metal foil layers and then heat-pressing them to form an integral piece of adhesive.
【0010】即ち本発明は、木質繊維又は木削片に熱硬
化性樹脂接着剤を添加し乾燥したものをコンベア上に落
下堆積して得られる木質堆積層と金属箔層とを交互に配
し、表裏に該木質堆積層が配置されるよう積層した後、
加熱圧締して接着一体成形することを特徴とする、複合
板の製造方法である。[0010] That is, the present invention alternately arranges wooden deposited layers obtained by adding a thermosetting resin adhesive to wood fibers or wood chips and drying them and depositing them on a conveyor and metal foil layers. , After laminating so that the woody deposited layer is placed on the front and back,
This is a method for manufacturing a composite board, which is characterized by integrally molding the composite board by heat-pressing and bonding.
【0011】本発明によって製造される複合板は図1に
略示されるように、金属箔層2の表面側及び裏面側に夫
々木質繊維層及び/又は木削片層(以下これらを総称し
て木質堆積層と言う)1a,1bが夫々積層接着された
サンドイッチ構造をなす。図1の構成例では、表面側及
び裏面側の木質堆積層1a,1bが略同一の厚さであっ
て、金属箔層2が複合板全体の厚さ方向において略中央
に配置されているが、図2に示すように、表面側の木質
堆積層1aを裏面側の木質堆積層1bよりも薄層として
金属箔層2が複合板の表面近傍に配置されるよう構成し
ても良い。また、表面側と裏面側の木質堆積層1a,1
bは、共に木質繊維層であっても、また共に木削片層で
あっても良く、或は表面層1aを木質繊維層として裏面
層1bを木削片層とし、或はその逆であっても良い。こ
れらの組み合わせは複合板の用途に応じて任意選択され
る。また木質堆積層及び金属箔層の数は限定的ではなく
、図3に示されるように複数の金属箔層2a,2bと複
数の木質堆積層1a,1b,1cとを交互に積層して表
裏面に木質堆積層が配置されるような構成のものであっ
ても良い。上記したような可変要因によって、同一厚さ
であっても種々の構成態様の複合板をその用途に応じて
得ることができる。As schematically shown in FIG. 1, the composite board manufactured according to the present invention has a wood fiber layer and/or a wood chip layer (hereinafter collectively referred to as these) on the front and back sides of the metal foil layer 2, respectively. (referred to as woody sedimentary layers) 1a and 1b form a sandwich structure in which layers 1a and 1b are laminated and bonded. In the configuration example shown in FIG. 1, the wood deposited layers 1a and 1b on the front side and the back side have approximately the same thickness, and the metal foil layer 2 is arranged approximately at the center in the thickness direction of the entire composite board. As shown in FIG. 2, the wood deposit layer 1a on the front side may be thinner than the wood deposit layer 1b on the back side, and the metal foil layer 2 may be arranged near the surface of the composite board. In addition, the woody deposited layers 1a, 1 on the front side and the back side
b may both be wood fiber layers or both wood chip layers, or the surface layer 1a may be a wood fiber layer and the back layer 1b a wood chip layer, or vice versa. It's okay. Any combination of these may be selected depending on the use of the composite plate. Furthermore, the number of wood deposited layers and metal foil layers is not limited, and as shown in FIG. It may also have a structure in which a woody deposited layer is placed on the back surface. Depending on the above-mentioned variable factors, it is possible to obtain composite plates with various configurations depending on their uses even if they have the same thickness.
【0012】本発明の製造方法において、例えばラワン
、カポール、栗、ポプラ等の広葉樹材又は松、杉、桧等
の針葉樹材をチップにした後、常法に従って解繊するこ
とによって得られる木質繊維、或は小径木、製材廃材、
原木むき芯、廃材チップ等を原料として切削及び破砕し
て得られる木削片を原料として用いる。[0012] In the production method of the present invention, wood fibers obtained by making chips from hardwoods such as lauan, capor, chestnut, and poplar, or from softwoods such as pine, cedar, and cypress, and then defibrating them according to a conventional method. , or small diameter wood, waste lumber,
Wood shavings obtained by cutting and crushing raw wood cores, waste wood chips, etc. are used as raw materials.
【0013】得られた木質繊維又は木削片に、尿素樹脂
系接着剤、フェノール樹脂系接着剤、メラミン樹脂系接
着剤、エポキシ樹脂系接着剤、ポリイソシアネート樹脂
系接着剤又はこれら複合樹脂接着剤等の熱硬化性樹脂接
着剤を添加する。これら熱硬化性樹脂接着剤の添加量は
、木質繊維又は木削片に対して10〜20重量%、その
樹脂率を30〜60%とすることが好ましい。接着剤は
低樹脂率の方が木質繊維に対して均一に混入することが
できる。[0013] A urea resin adhesive, a phenol resin adhesive, a melamine resin adhesive, an epoxy resin adhesive, a polyisocyanate resin adhesive, or a composite resin adhesive thereof is applied to the obtained wood fibers or wood chips. Add a thermosetting resin adhesive such as The amount of these thermosetting resin adhesives added is preferably 10 to 20% by weight based on the wood fibers or wood chips, and the resin percentage is preferably 30 to 60%. The adhesive can be more uniformly mixed into the wood fibers if the resin content is low.
【0014】金属箔層としては、鉄、アルミニウム、ス
テンレス、銅等の金属又は合金であって厚さ20〜10
0μの金属箔が好適に用いられる。この金属箔の表面に
は必要に応じてメッキ処理等の防錆処理が施される。ま
た、金属箔に微小孔を複数設けてメッシュ状としたもの
や、金属糸を用いて織った金属織布を、本発明における
金属箔層として用いることもできる。このようにして微
小孔等により通気性を持たせた金属箔を用いることによ
り、接着剤を添加乾燥した木質繊維又は木削片中に残存
する水分が加熱圧締の際に外に逃げようとする動きが規
制されなくなるので、解圧の際に生ずるパンク現象を有
効に防止することができる。The metal foil layer is made of metal or alloy such as iron, aluminum, stainless steel, copper, etc., and has a thickness of 20 to 10
0μ metal foil is preferably used. The surface of this metal foil is subjected to antirust treatment such as plating treatment, if necessary. Further, metal foil with a plurality of micropores formed into a mesh shape, or a metal woven fabric woven using metal threads can also be used as the metal foil layer in the present invention. By using metal foil that has air permeability through micro holes, etc., moisture remaining in the wood fibers or wood shavings that have been added with adhesive and dried will be able to escape during heating and compaction. Since the movement of the pump is no longer restricted, it is possible to effectively prevent a puncture phenomenon that occurs when the pressure is released.
【0015】本発明方法に従って複合板を製造する工程
について、木質繊維層を設ける場合を例としてより詳細
に説明すると、前記針葉樹材又は広葉樹材のチップを高
温高圧蒸気下で蒸煮して脱脂軟化処理した後、解繊装置
によって解繊して木質繊維を得る。この木質繊維は長さ
が1〜30mm、太さが直径2〜300μ程度のものが
大半を占め、木材の細胞や導管孔或は仮導管孔から成る
細胞孔が数本ないし数十本束になった形をしており、繊
維外周部の細胞壁は引き裂かれたり割れ目を生じたりし
ていることが多いため、湿気や水分を多く吸収する。To explain in more detail the process of manufacturing a composite board according to the method of the present invention, taking as an example the case where a wood fiber layer is provided, the softwood or hardwood chips are steamed under high temperature and high pressure steam to be degreased and softened. After that, it is defibrated using a defibrating device to obtain wood fibers. Most of these wood fibers are 1 to 30 mm long and 2 to 300 μm in diameter, and are bundled with several to dozens of cell pores consisting of wood cells, duct pores, or tracheid pores. It has a rounded shape, and the cell walls around the fibers are often torn or cracked, so they absorb a lot of moisture and moisture.
【0016】得られた木質繊維を乾燥装置により乾燥し
た後、混合装置に投入して、前記熱硬化性樹脂接着剤を
添加混合する。混合装置においては必要に応じてサイズ
剤、発水剤、減煙剤等任意添加剤を同時に混合すること
ができる。After the obtained wood fibers are dried in a drying device, they are put into a mixing device, and the thermosetting resin adhesive is added and mixed therein. In the mixing device, arbitrary additives such as a sizing agent, a water generating agent, a smoke reducing agent, etc. can be mixed at the same time as necessary.
【0017】熱硬化性樹脂接着剤を付着された木質繊維
は、次いで熱風ダクト中を風送搬送しながら乾燥する。
この際の風送速度は木質繊維の比重、送り量、前後の工
程の処理能力等によって広範囲に調整されるが、一般に
約15〜20m/秒とされる。この熱風による風送で木
質繊維は6〜15%程度の水分量まで乾燥される。The wood fibers to which the thermosetting resin adhesive has been adhered are then dried while being conveyed through a hot air duct. The air blowing speed at this time can be adjusted over a wide range depending on the specific gravity of the wood fiber, the amount of feed, the processing capacity of the previous and subsequent steps, etc., but is generally about 15 to 20 m/sec. This hot air blowing dries the wood fibers to a moisture content of about 6 to 15%.
【0018】乾燥された木質繊維はフォーミング装置に
投入され、コンベア上に落下させて木質繊維堆積層を形
成する。図4は図3に示される構成の複合板を製造する
際に用いられる装置全般の概略構成を示し、木質繊維を
落下堆積させるフォーミング装置10a,10b,10
cの間に金属箔を供給する金属箔ロール20a,20b
を夫々配置し、木質繊維堆積層と金属箔とが交互に積層
された積層体12を形成した後、切断機14によって適
宜寸法に切断して定寸積層体16とし、これをホットプ
レス18に投入して加熱圧締することによって目的とす
る図3の如き複合板が得られる。木質繊維堆積層と金属
箔とを積層する際に、金属箔の表裏面に、木質繊維に添
加混合した接着剤と同様の熱硬化性樹脂接着剤を予め塗
布しておくことにより、複合板の接着強度を更に向上さ
せることができる。The dried wood fibers are put into a forming device and dropped onto a conveyor to form a wood fiber pile layer. FIG. 4 shows a schematic configuration of the overall apparatus used when manufacturing the composite board having the configuration shown in FIG.
Metal foil rolls 20a and 20b supplying metal foil between c.
After forming a laminate 12 in which wood fiber deposited layers and metal foils are alternately laminated, the cutter 14 cuts the laminate 16 into a fixed size laminate 16, which is then placed in a hot press 18. The desired composite plate as shown in FIG. 3 is obtained by charging and heating and pressing. When laminating the wood fiber deposit layer and the metal foil, by applying a thermosetting resin adhesive similar to the adhesive mixed with the wood fibers on the front and back surfaces of the metal foil, the composite board Adhesive strength can be further improved.
【0019】本発明によって製造される複合板を高度の
防火性能が要求される場面に使用する場合には、少なく
とも表面側に配される木質繊維層/木削片層1aを得る
に当たって、その木質繊維又は木削片に予め防火処理を
施しておくことが好ましい。この防火処理は、例えば、
熱硬化性樹脂接着剤が添加される前の木質繊維又は木削
片の、細胞孔内の空隙部及び/又は細胞孔内壁面及び/
又は該木質繊維又は木削片の外周部に不燃性無機化合物
を充填又は付着或は固着せしめるべく処理するものであ
って、この処理について木質繊維の場合を例として詳述
すると以下の通りである。When the composite board manufactured by the present invention is used in a situation where a high degree of fire prevention performance is required, the wood fiber layer/wood chip layer 1a arranged at least on the surface side is obtained by It is preferable that the fibers or wood chips are subjected to fireproofing treatment in advance. This fire prevention treatment is, for example,
The voids within the cell pores and/or the inner wall surface of the cell pores and/or the wood fibers or wood chips before the thermosetting resin adhesive is added.
Alternatively, the outer periphery of the wood fibers or wood chips is treated with a nonflammable inorganic compound to be filled with, adhered to, or fixed to the outer periphery of the wood fibers or wood chips, and the details of this treatment are as follows, taking the case of wood fibers as an example. .
【0020】即ち、熱硬化性樹脂接着剤が添加される前
であって乾燥装置において適宜乾燥処理された直後の木
質繊維を水溶性無機塩の水溶液(以下「第1液」と称す
)中に十分に浸漬させて含浸させる。この際、減圧又は
加圧を加えて含浸処理を強制的に促進させると有効であ
る。また木質繊維を乾燥することなく高含水率状態とし
て、或は一旦乾燥した後に水または温水に浸漬して吸水
させこれを飽水状態とした後に、第1液中に浸漬させて
拡散含浸させても良い。第1液としては、MgCl2,
MgBr2,MgSO4・H2O,Mg(NO3)2・
6H2O,AlCl3,AlBr3,Al2(SO4)
3,Al(NO3)3・9H2O,CaCl2,CaB
r2,Ca(NO3)2,ZnCl2,BaBr2,B
aCl2・2H2O,Ba(NO3)2等の水溶液が例
示される。木質繊維を第1液に浸漬含浸せしめることに
よって溶質の無機塩のイオンが拡散により木質繊維の細
胞孔内にまで入り込む。That is, before the thermosetting resin adhesive is added, the wood fibers have just been properly dried in a drying device and are placed in an aqueous solution of a water-soluble inorganic salt (hereinafter referred to as the "first liquid"). Soak and soak thoroughly. At this time, it is effective to forcibly accelerate the impregnation treatment by applying reduced pressure or increased pressure. Alternatively, the wood fibers may be brought into a high moisture content state without being dried, or once dried, immersed in water or warm water to absorb water to saturate the wood fibers, and then immersed in the first liquid for diffusion impregnation. Also good. As the first liquid, MgCl2,
MgBr2, MgSO4・H2O, Mg(NO3)2・
6H2O, AlCl3, AlBr3, Al2(SO4)
3, Al(NO3)3・9H2O, CaCl2, CaB
r2, Ca(NO3)2, ZnCl2, BaBr2, B
Examples include aqueous solutions such as aCl2.2H2O and Ba(NO3)2. By immersing the wood fibers in the first solution, ions of the inorganic salt of the solute diffuse into the cell pores of the wood fibers.
【0021】次いで余剰分の第1液を除去するために脱
液処理を行う。脱液処理は例えば遠心脱液或はシャワー
、どぶ漬けの水洗い等の手段によって行われ、余剰分の
第1液を除去することによって木質繊維表面において不
燃性無機化合物が過剰に生成されることを抑制し、次に
含浸される水溶液の拡散含浸を良好にする。また木質繊
維に付着又は固着されない遊離状態で不燃性無機化合物
が生成されることを防止する。脱液処理後、必要に応じ
て、表面に析出した第1液の成分結晶を除去する。[0021] Next, a liquid removal process is performed to remove the excess first liquid. The liquid removal treatment is carried out by means such as centrifugal liquid removal, showering, and soaking in water, and by removing the excess first liquid, it is possible to avoid excessive production of nonflammable inorganic compounds on the surface of the wood fibers. suppresses and improves diffusion impregnation of the aqueous solution to be impregnated next. It also prevents nonflammable inorganic compounds from being produced in a free state that is not attached or fixed to wood fibers. After the liquid removal treatment, component crystals of the first liquid deposited on the surface are removed, if necessary.
【0022】次いで、第1液と反応して水不溶性の不燃
性無機化合物を生成するような化合物液(以下「第2液
」と称す)をブレンダー,スプレー等を用いて木質繊維
に添加混合し或は浸漬せしめることによって、該第2液
を木質繊維に含浸させる。第1液の場合と同様に、減圧
又は加圧処理によって木質繊維に対する第2液の含浸を
促進せしめることができる。第2液としては、Na2C
O3,H2SO4,(NH4)2CO3,Na2SO4
,(NH4)2SO4,H2PO4,Na2HPO4,
(NH4)2HPO4,H3BO3,NaBO2,NH
4BO2等が例示される。第2液を塗布ないし浸漬する
ことにより木質繊維の細胞孔内に該第2液が拡散含浸さ
れ、木質繊維中で第1液と第2液とが反応し、不燃性無
機化合物が生成される。生成される不燃性無機化合物と
しては、リン酸マグネシウム,リン酸カルシウム,リン
酸バリウム,リン酸アルミニウム,ホウ酸マグネシウム
,炭酸マグネシウム,炭酸カルシウム,リン酸亜鉛,炭
酸バリウム,硝酸カルシウム,硝酸バリウム等のカルシ
ウム化合物、マグネシウム化合物、アルミニウム化合物
、バリウム化合物、鉛化合物、亜鉛化合物、ケイ酸化合
物等が例示される。例えば第1液として塩化バリウムを
用い、第2液としてリン酸水素アンモニウムを用いて反
応させると、バリウムのカチオンとリン酸のアニオンと
が反応して、リン酸バリウムとリン酸水素バリウムとが
生成される。Next, a compound liquid that reacts with the first liquid to produce a water-insoluble, nonflammable inorganic compound (hereinafter referred to as the "second liquid") is added to and mixed with the wood fibers using a blender, spray, etc. Alternatively, the wood fibers are impregnated with the second liquid by dipping. As in the case of the first liquid, impregnation of the second liquid into the wood fibers can be promoted by reducing or pressurizing the wood fibers. As the second liquid, Na2C
O3, H2SO4, (NH4)2CO3, Na2SO4
, (NH4)2SO4, H2PO4, Na2HPO4,
(NH4)2HPO4, H3BO3, NaBO2, NH
An example is 4BO2. By applying or dipping the second liquid, the second liquid is diffused and impregnated into the cell pores of the wood fiber, and the first liquid and the second liquid react in the wood fiber, producing a nonflammable inorganic compound. . Nonflammable inorganic compounds produced include calcium compounds such as magnesium phosphate, calcium phosphate, barium phosphate, aluminum phosphate, magnesium borate, magnesium carbonate, calcium carbonate, zinc phosphate, barium carbonate, calcium nitrate, and barium nitrate. , magnesium compounds, aluminum compounds, barium compounds, lead compounds, zinc compounds, silicate compounds, and the like. For example, if barium chloride is used as the first liquid and ammonium hydrogen phosphate is used as the second liquid, the barium cations and phosphoric acid anions will react, producing barium phosphate and barium hydrogen phosphate. be done.
【0023】反応終了後、遠心脱液或はシャワー、どぶ
漬け等による水洗い等の手段によって脱液処理して余剰
分の第2液を除去する。第2液の浸漬処理及び脱液処理
は必要に応じて複数回反復して行っても良い。脱液処理
後、乾燥してその含水率を25%以下、好ましくは7〜
15%とする。この不燃性無機化合物は水不溶性である
ため、乾燥後において、木質繊維の細胞孔内又は細胞孔
内壁面に充填ないし付着或は固着されると共に木質繊維
外周部にも付着或は固着される。これにより、木質繊維
表面に現出される空隙孔や割れ目を閉塞ないし充填する
ような形で不燃性無機化合物が存在することとなる。[0023] After the reaction is completed, the excess second liquid is removed by deliquification treatment by means such as centrifugal deliquidation or washing with water such as showering or soaking. The second liquid immersion process and the liquid removal process may be repeated multiple times as necessary. After the liquid removal treatment, dry to reduce the moisture content to 25% or less, preferably 7 to 7%.
It shall be 15%. Since this nonflammable inorganic compound is water-insoluble, after drying, it fills in, adheres to, or adheres to the inside of the cell pores of the wood fibers or the inner wall surface of the cell pores, and also adheres to or adheres to the outer periphery of the wood fibers. As a result, the nonflammable inorganic compound is present in a form that blocks or fills the pores and cracks appearing on the surface of the wood fibers.
【0024】不燃性無機化合物は、木質繊維に対して3
3重量%以上の割合で混入されることが好ましく、これ
以下では十分な防火性能が得られない。また第1液と第
2液との反応効率を高めるために、第2液の添加混合は
加熱雰囲気下、特に40℃以上更に好ましくは50℃以
上の温度で行うことが好ましい。また第1液と第2液を
温水状態としてこれに木質繊維を浸漬せしめ、あるいは
第1液及び第2液の浸漬時に超音波やバイブレータ等に
よって電気的或は機械的振動を与えるようにすると、木
質繊維中への処理液の拡散並びに反応が良好に行われる
。なお第1液と第2液とによる処理順序は問わず、先に
第2液による処理を行っても勿論良い。[0024] The nonflammable inorganic compound is
It is preferable that it is mixed in at a ratio of 3% by weight or more, and if it is less than this, sufficient fire protection performance cannot be obtained. Further, in order to increase the reaction efficiency between the first liquid and the second liquid, it is preferable that the addition and mixing of the second liquid is carried out under a heated atmosphere, particularly at a temperature of 40°C or higher, more preferably 50°C or higher. Furthermore, if the first liquid and the second liquid are heated and the wood fibers are immersed therein, or when the wood fibers are immersed in the first liquid and the second liquid, electrical or mechanical vibrations are applied using ultrasonic waves, a vibrator, etc. Diffusion and reaction of the treatment liquid into the wood fibers are carried out well. Note that the order of processing with the first liquid and the second liquid does not matter, and it goes without saying that the processing with the second liquid may be performed first.
【0025】かくして、木質繊維の細胞孔内または内壁
面に不燃性無機化合物が固着され且つその外周部にも不
燃性無機化合物が固着または付着されて防火処理された
木質繊維が得られる。この防火処理された木質繊維は前
記したように混合装置に投入されて熱硬化性樹脂接着剤
が添加混合される。[0025] In this manner, a fireproof treated wood fiber is obtained in which the nonflammable inorganic compound is fixed to the cell pores or the inner wall surface of the wood fiber, and the nonflammable inorganic compound is also fixed or attached to the outer periphery of the wood fiber. The fireproof treated wood fibers are put into a mixing device as described above, and a thermosetting resin adhesive is added and mixed therein.
【0026】なお木質繊維又は木削片に対する防火処理
は上記した方法以外の方法によっても良い。例えば、従
来より防火薬剤として公知の物質、例えば、リン酸アン
モニウム、硫酸アンモニウム、臭化アンモニウム等のア
ンモニウム塩、炭酸カリウム、炭酸ナトリウム、リン酸
カリウム等のアルカリ金属塩、塩化カルシウム、塩化マ
グネシウム等のアルカリ土類金属塩、塩化アルミニウム
、硫酸アルミニウム等の金属化合物等の溶液中に木質繊
維又は木削片を浸漬含浸させた後乾燥することによって
も行うことができる。[0026] The fire prevention treatment for the wood fibers or wood chips may be performed by a method other than the above-mentioned method. For example, substances conventionally known as fire retardants, such as ammonium salts such as ammonium phosphate, ammonium sulfate, and ammonium bromide, alkali metal salts such as potassium carbonate, sodium carbonate, and potassium phosphate, and alkalis such as calcium chloride and magnesium chloride. It can also be carried out by impregnating wood fibers or wood chips in a solution of metal compounds such as earth metal salts, aluminum chloride, aluminum sulfate, etc., followed by drying.
【0027】[0027]
[実施例1]
ラジアータパインのチップを160℃、7kg/cm2
で5分間煮沸して脱脂軟化処理を行った。このチップを
デファイブレータ式リファイナで解繊し、得られた木質
繊維を乾燥した。この木質繊維を塩化バリウム30%水
溶液に10分間浸漬し、拡散処理した後脱液した。これ
を熱風乾燥してその含水率を7%に調整した。この木質
繊維をブレンダ装置に投入してリン酸アンモニウム40
%水溶液を添加混合し、該木質繊維の細胞孔等の孔内及
び木質繊維外周部に水不溶性のリン酸バリウムとリン酸
水素バリウムとから成る不燃性無機化合物を生成させた
後脱液水洗し、熱風乾燥してその含水率を6%に調整し
た。この防火処理による木質繊維の重量増加率は40%
であった。[Example 1] Radiata pine chips at 160°C and 7 kg/cm2
It was boiled for 5 minutes to perform a defatting and softening treatment. The chips were defibrated using a defibrator refiner, and the resulting wood fibers were dried. This wood fiber was immersed in a 30% barium chloride aqueous solution for 10 minutes, subjected to a diffusion treatment, and then drained. This was dried with hot air to adjust its moisture content to 7%. This wood fiber is put into a blender device and ammonium phosphate is mixed with 40% of ammonium phosphate.
% aqueous solution is added and mixed to generate a nonflammable inorganic compound consisting of water-insoluble barium phosphate and barium hydrogen phosphate inside the cell pores of the wood fibers and on the outer periphery of the wood fibers, and then deliquified and washed with water. The moisture content was adjusted to 6% by hot air drying. The weight increase rate of wood fibers due to this fireproofing treatment is 40%.
Met.
【0028】防火処理された木質繊維をブレンダーに投
入し、該ブレンダー内において木質繊維量に対して4%
のワックスサイズ剤及び10%のフェノール樹脂接着剤
を添加混合した後、フォーミング装置に搬送し、スクリ
ーンコンベア上に落下させ堆積させて木質繊維堆積層を
形成した。[0028] Fireproof treated wood fibers are put into a blender, and in the blender 4% of the amount of wood fibers is added.
After adding and mixing a wax sizing agent of 10% and a phenolic resin adhesive of 10%, the mixture was conveyed to a forming device and dropped onto a screen conveyor to be deposited to form a wood fiber deposit layer.
【0029】スクリーンコンベア上には、このようにし
て3層の木質繊維堆積層を形成する第1乃至第3のフォ
ーミング装置及び夫々45μm厚の鉄箔を供給する第1
及び第2の鉄箔供給ロールを、図4のように、コンベア
搬送方向下流側から第1のフォーミング装置、第1の鉄
箔供給ロール、第2のフォーミング装置、第2の鉄箔供
給ロール、第3のフォーミング装置の順に配置して、表
面側から木質繊維堆積層/鉄箔/木質繊維堆積層/鉄箔
/木質繊維堆積層の順に堆積された連続状マットを得た
。On the screen conveyor, there are first to third forming devices that form three wood fiber deposit layers in this way, and a first forming device that supplies iron foil each having a thickness of 45 μm.
And the second iron foil supply roll, as shown in FIG. 4, from the downstream side in the conveyor conveyance direction, the first forming device, the first iron foil supply roll, the second forming device, the second iron foil supply roll, The third forming device was arranged in this order to obtain a continuous mat in which wood fiber deposited layer/iron foil/wood fiber deposited layer/iron foil/wood fiber deposited layer was deposited in this order from the surface side.
【0030】このようにして得られた連続状マットを適
当な長さに切断した後、ホットプレスに挿入して200
℃にて5分間熱圧成形して、厚さ13mm、比重0.6
5の複合板を得た。After cutting the continuous mat thus obtained to an appropriate length, it was inserted into a hot press and heated for 200 minutes.
Heat-press molded at ℃ for 5 minutes, thickness 13 mm, specific gravity 0.6
A composite board of No. 5 was obtained.
【0031】この複合板について加熱試験を行ったとこ
ろ、凖不燃材料に合格する防火性能を示すことが確認さ
れた。[0031] When this composite plate was subjected to a heating test, it was confirmed that it exhibited fireproof performance that passed the test as a noncombustible material.
【0032】
[実施例2]
ラジアータパイン原木又は廃材をフレーカに投入してフ
レーク状の木削片を得た。この木削片を乾燥した後仕分
けして、適性フレーク状の木削片を収集した。この木削
片を実施例1の木質繊維の場合と同様にして防火処理し
た後、連続式ミキサーに投入し、該ミキサー内において
木削片量に対し1%のワックスサイズ剤及び8%のフェ
ノール樹脂接着剤を添加混合した後、フォーミング装置
に搬送し、スクリーンコンベア上に落下させ堆積させた
。[Example 2] Radiata pine raw wood or waste wood was put into a flaker to obtain flaky wood chips. After drying, the wood chips were sorted to collect appropriate flaky wood chips. After the wood chips were fireproofed in the same manner as in the case of the wood fibers in Example 1, they were put into a continuous mixer, and in the mixer, 1% wax sizing agent and 8% phenol were added to the amount of wood chips. After the resin adhesive was added and mixed, it was conveyed to a forming device and dropped onto a screen conveyor to be deposited.
【0033】スクリーンコンベア上において、実施例1
と同様にして、表面側から木削片堆積層/鉄箔/木削片
堆積層/鉄箔/木削片堆積層の順に堆積された連続状マ
ットを得た。On the screen conveyor, Example 1
In the same manner as above, a continuous mat was obtained in which the following steps were deposited in the order of wood chip deposit layer/iron foil/wood chip deposit layer/iron foil/wood chip deposit layer from the surface side.
【0034】このようにして得られた連続状マットを適
当な長さに切断した後、ホットプレスに挿入して200
℃にて5分間熱圧成形して、厚さ13mm、比重0.5
の複合板を得た。After cutting the continuous mat thus obtained to an appropriate length, it was inserted into a hot press and heated for 200 minutes.
Heat-press molded at ℃ for 5 minutes, thickness 13 mm, specific gravity 0.5
A composite board was obtained.
【0035】この複合板について加熱試験を行ったとこ
ろ、凖不燃材料に合格する防火性能を示すことが確認さ
れた。[0035] When this composite board was subjected to a heating test, it was confirmed that it exhibited fireproof performance that passed the test as a noncombustible material.
【0036】[0036]
【発明の効果】本発明方法によれば、接着剤を塗布乾燥
させた状態の木質繊維又は木削片を用い、これをフォー
ミング装置によりコンベア上に堆積する際に金属箔と交
互に積層するものであるために、作業効率に優れ、また
熱圧後の解圧時にもパンクを生じさせることがない。従
って寸法安定性に優れ防火性能の向上された複合板を効
率的に製造することができる。[Effects of the Invention] According to the method of the present invention, wood fibers or wood shavings coated with an adhesive and dried are used, and when deposited on a conveyor by a forming device, they are laminated alternately with metal foil. Therefore, it has excellent work efficiency and does not cause punctures even when depressurizing after hot pressing. Therefore, a composite board with excellent dimensional stability and improved fireproof performance can be efficiently produced.
【図1】本発明方法によって製造される複合板の構成の
一例を示す斜視図である。FIG. 1 is a perspective view showing an example of the structure of a composite plate manufactured by the method of the present invention.
【図2】本発明方法によって製造される複合板の他の構
成例を示す斜視図である。FIG. 2 is a perspective view showing another structural example of a composite plate manufactured by the method of the present invention.
【図3】本発明方法によって製造される複合板の他の構
成例を示す斜視図である。FIG. 3 is a perspective view showing another structural example of a composite plate manufactured by the method of the present invention.
【図4】図3の複合板を製造する際に用いられる装置の
概略構成を示す説明図である。4 is an explanatory diagram showing a schematic configuration of an apparatus used when manufacturing the composite plate of FIG. 3. FIG.
1a 木質堆積層 1b 木質堆積層 1c 木質堆積層 2 金属箔層 2a 金属箔層 2b 金属箔層 1a Woody sediment layer 1b Woody sediment layer 1c Woody sediment layer 2 Metal foil layer 2a Metal foil layer 2b Metal foil layer
Claims (4)
脂接着剤を添加し乾燥させたものをコンベア上に落下堆
積して得られる木質堆積層と、金属箔層とを、交互に配
して表裏に前記木質堆積層が配置されるよう積層した後
、加熱圧締して接着一体成形することを特徴とする、複
合板の製造方法。Claim 1: Wooden deposited layers obtained by adding a thermosetting resin adhesive to wood fibers or wood chips and drying them are deposited on a conveyor, and metal foil layers are alternately arranged. A method for manufacturing a composite board, which comprises laminating the wood deposited layers on the front and back sides, and then heat-pressing and bonding and integrally forming the composite board.
樹脂接着剤を塗布した後、前記木質マットと積層する、
請求項1記載の複合板の製造方法。2. After applying a thermosetting resin adhesive to the front and back surfaces of the metal foil layer, laminating it with the wood mat;
A method for manufacturing a composite board according to claim 1.
数有する金属箔が用いられる、請求項1記載の複合板の
製造方法。3. The method for manufacturing a composite plate according to claim 1, wherein a metal foil having a plurality of micropores is used as the metal foil layer.
火処理を施す、請求項1乃至3のいずれか記載の複合板
の製造方法。4. The method for manufacturing a composite board according to claim 1, wherein the wood fibers or wood chips are subjected to fire prevention treatment in advance.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2410728A JP2663049B2 (en) | 1990-12-14 | 1990-12-14 | Manufacturing method of composite board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2410728A JP2663049B2 (en) | 1990-12-14 | 1990-12-14 | Manufacturing method of composite board |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04216044A true JPH04216044A (en) | 1992-08-06 |
JP2663049B2 JP2663049B2 (en) | 1997-10-15 |
Family
ID=18519842
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2410728A Expired - Fee Related JP2663049B2 (en) | 1990-12-14 | 1990-12-14 | Manufacturing method of composite board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2663049B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4870037A (en) * | 1987-09-23 | 1989-09-26 | Vesuvius Crucible Company | Prevention of Al2 O3 formation in pouring nozzles and the like |
US4871698A (en) * | 1987-11-09 | 1989-10-03 | Vesuvius Crucible Company | Carbon bonded refractory bodies |
KR100431639B1 (en) * | 2001-07-12 | 2004-05-17 | 이순노 | Board binding method and chassis |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61293804A (en) * | 1985-06-21 | 1986-12-24 | Iwakuragumi Mokuzai Kk | Manufacture of particle board for shielding electromagnetic wave |
-
1990
- 1990-12-14 JP JP2410728A patent/JP2663049B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61293804A (en) * | 1985-06-21 | 1986-12-24 | Iwakuragumi Mokuzai Kk | Manufacture of particle board for shielding electromagnetic wave |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4870037A (en) * | 1987-09-23 | 1989-09-26 | Vesuvius Crucible Company | Prevention of Al2 O3 formation in pouring nozzles and the like |
US4871698A (en) * | 1987-11-09 | 1989-10-03 | Vesuvius Crucible Company | Carbon bonded refractory bodies |
KR100431639B1 (en) * | 2001-07-12 | 2004-05-17 | 이순노 | Board binding method and chassis |
Also Published As
Publication number | Publication date |
---|---|
JP2663049B2 (en) | 1997-10-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2663049B2 (en) | Manufacturing method of composite board | |
JP2646158B2 (en) | Manufacturing method of composite board | |
JP2589218B2 (en) | Manufacturing method of composite board | |
JP7041765B1 (en) | A method for manufacturing an impregnated paper for a decorative base material, a method for manufacturing a decorative base material, and a method for manufacturing a decorative board. | |
JP2589217B2 (en) | Manufacturing method of composite board | |
JP2603881B2 (en) | Composite plate and method of manufacturing the same | |
JPH04176642A (en) | Composite sheet | |
JP2603882B2 (en) | Composite plate and method of manufacturing the same | |
JPH04176641A (en) | Composite sheet | |
JP2627133B2 (en) | Improved wood fiber board and method for producing the same | |
JP2663055B2 (en) | Wood fiberboard for molding and method for producing the same | |
JPH04122638A (en) | Composite board and manufacture thereof | |
JPH04122637A (en) | Composite board and manufacture thereof | |
JP2626728B2 (en) | Decorative plate and manufacturing method thereof | |
JPH04216045A (en) | Decorative panel and manufacture thereof | |
JPH03258509A (en) | Non-combustible organic fiber-board and manufacture thereof | |
JP2688602B2 (en) | Decorative plate and manufacturing method thereof | |
JPH03258503A (en) | Non-combustible laminate and manufacture thereof | |
JP2688599B2 (en) | Decorative plate and manufacturing method thereof | |
JPH04351502A (en) | Improved wooden fiber-plate and its manufacture | |
JP2540222Y2 (en) | Laminated board | |
JPH04115081A (en) | Fire door | |
JP2521175B2 (en) | Composite material and manufacturing method thereof | |
JPH03258539A (en) | Composite and its manufacture | |
JPH03258508A (en) | Non-combustible chip-board and manufacture thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |