JPH09209299A - Composite board and its production - Google Patents
Composite board and its productionInfo
- Publication number
- JPH09209299A JPH09209299A JP1615596A JP1615596A JPH09209299A JP H09209299 A JPH09209299 A JP H09209299A JP 1615596 A JP1615596 A JP 1615596A JP 1615596 A JP1615596 A JP 1615596A JP H09209299 A JPH09209299 A JP H09209299A
- Authority
- JP
- Japan
- Prior art keywords
- inorganic filler
- surface area
- cellulosic fiber
- composite plate
- weight
- 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 40
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 239000000835 fiber Substances 0.000 claims abstract description 43
- 239000011256 inorganic filler Substances 0.000 claims abstract description 37
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 37
- 239000010440 gypsum Substances 0.000 claims abstract description 30
- 229910052602 gypsum Inorganic materials 0.000 claims abstract description 30
- 239000002699 waste material Substances 0.000 claims abstract description 23
- 229920005989 resin Polymers 0.000 claims abstract description 22
- 239000011347 resin Substances 0.000 claims abstract description 22
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 21
- 239000002002 slurry Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000003825 pressing Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 238000010030 laminating Methods 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 27
- 239000002023 wood Substances 0.000 abstract description 17
- 239000000203 mixture Substances 0.000 abstract description 10
- 239000002440 industrial waste Substances 0.000 abstract description 3
- 238000007731 hot pressing Methods 0.000 abstract 1
- 239000005011 phenolic resin Substances 0.000 description 23
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- 239000000047 product Substances 0.000 description 15
- 238000005520 cutting process Methods 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 11
- 229910000019 calcium carbonate Inorganic materials 0.000 description 10
- 239000000123 paper Substances 0.000 description 10
- -1 shirasu balloon Substances 0.000 description 10
- 239000002655 kraft paper Substances 0.000 description 9
- 229920001568 phenolic resin Polymers 0.000 description 9
- 125000001743 benzylic group Chemical group 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000011122 softwood Substances 0.000 description 7
- 239000003365 glass fiber Substances 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 238000005452 bending Methods 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 239000011120 plywood Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920003986 novolac Polymers 0.000 description 4
- 229920003987 resole Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000009423 ventilation Methods 0.000 description 4
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 150000004683 dihydrates Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 239000010456 wollastonite Substances 0.000 description 3
- 229910052882 wollastonite Inorganic materials 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
- 239000005995 Aluminium silicate Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 239000004113 Sepiolite Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- UGGQKDBXXFIWJD-UHFFFAOYSA-N calcium;dihydroxy(oxo)silane;hydrate Chemical compound O.[Ca].O[Si](O)=O UGGQKDBXXFIWJD-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910052624 sepiolite Inorganic materials 0.000 description 2
- 235000019355 sepiolite Nutrition 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 244000233967 Anethum sowa Species 0.000 description 1
- 238000004438 BET method Methods 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 206010016807 Fluid retention Diseases 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- OJMOMXZKOWKUTA-UHFFFAOYSA-N aluminum;borate Chemical compound [Al+3].[O-]B([O-])[O-] OJMOMXZKOWKUTA-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- 239000011230 binding agent Substances 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
- 235000009120 camo Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000000779 depleting effect Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000003562 lightweight material Substances 0.000 description 1
- 230000004199 lung function Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、木材系あるいは木
質系材料(以下、単に木材系材料という)の代替材料と
して、セルロース系繊維と無機質フィラー、特に石膏ボ
ード廃材を有効利用してなる軽量で強度に優れ、かつ良
好な加工性を有する複合板及びその製造方法に関するも
のである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is a lightweight material which effectively utilizes cellulosic fibers and inorganic fillers, particularly gypsum board waste materials, as an alternative material for wood-based or wood-based materials (hereinafter simply referred to as wood-based materials). The present invention relates to a composite plate having excellent strength and good workability, and a method for manufacturing the same.
【0002】[0002]
【従来の技術】従来、建築土木分野において多量に用い
られている木材系材料は、世界的な木材資源の枯渇及び
自然環境の保護の観点から近未来には木材の入手が困難
になるものと予測される。2. Description of the Related Art Conventionally, wood-based materials that have been used in large amounts in the field of construction and civil engineering are expected to make it difficult to obtain wood in the near future from the viewpoint of depleting global wood resources and protecting the natural environment. is expected.
【0003】また、かかる木材系材料と同様に多用され
ている繊維質面材付き石膏ボードは、生産量の約20%
が廃材として発生し、そのうち生産現場で発生する一部
のものについては、面材すなわち紙を剥がして微粉砕
し、石膏成分の代替原料として再利用されている。しか
しながら、流通過程ないし工事現場から発生する該石膏
ボード廃材の粉砕物には、一般に面材由来のセルロース
系繊維分が含まれているため、高濃度の石膏スラリーを
用いる現行石膏ボード製法では、生産性に影響を及ぼす
スラリー流動の悪化を生じない10重量%程度が使用限
界とされており、その多くは再利用されることなく産業
廃棄物として処分されている。さらに、近年では処分場
の確保という問題も絡み、由々しき事態として注視され
ている。Further, the gypsum board with the fibrous surface material, which is widely used like the wood-based material, accounts for about 20% of the production amount.
Is generated as a waste material, and a part of the waste material generated at the production site is reused as a substitute raw material for the gypsum component after peeling the face material, that is, the paper, and pulverizing it. However, since the crushed product of the gypsum board waste material generated from the distribution process or the construction site generally contains a cellulose fiber component derived from a face material, the current gypsum board manufacturing method using a high-concentration gypsum slurry produces The limit of use is about 10% by weight, which does not cause deterioration of slurry flow that affects the property, and most of them are disposed of as industrial waste without being reused. Furthermore, in recent years, the problem of securing a disposal site has become involved, and it is being watched as a serious situation.
【0004】また難燃紙または難燃ボードの製造方法と
して、セルロース繊維、含水無機化合物、粉体状合成樹
脂、およびガラス繊維を配合して抄造し、場合によりこ
の表面に紙を積層した成形体も知られている(特開平4
−185799号公報)。しかしながら、このように繊
維補強効果を得るためにガラス繊維を使用する場合、セ
ルロース繊維と異なり、加工性、特に切削時の抵抗が問
題となる。すなわち、ガラス繊維が単繊維状態で分散し
ているならば問題ないが、数本から数十本収束されたま
ま、成形体内に分散した場合、断続的に大きな抵抗を示
し、円滑な切削が困難になる。またさらに切削を強行す
れば、収束したガラス繊維周辺の硬化体組織を破壊する
可能性が高くなる。また、この成形体中に用いられてい
る直径4μm以下の微細なガラス繊維は、加工に伴い発
生する粉塵中に一部粉状化されて浮遊し、作業環境を悪
化させる。粉状化されたガラス繊維は、作業従事者への
付着、それに伴うかゆみの発症、さらには皮膚疾患へと
人体に対する影響が懸念される。さらに、アスベストと
同様に、肺機能に影響するとの見解もあり、切削、加工
する用途への工業製品としては受け入れられるものでは
ない。Further, as a method for producing flame-retardant paper or flame-retardant board, cellulose fiber, hydrous inorganic compound, powdered synthetic resin, and glass fiber are blended into a papermaking product, and a paper product is laminated on the surface of the molded product in some cases. Is also known (Japanese Patent Laid-Open No. Hei 4)
-185799). However, when the glass fiber is used to obtain the fiber reinforcing effect as described above, unlike the cellulose fiber, the workability, particularly the resistance during cutting becomes a problem. That is, there is no problem if the glass fibers are dispersed in a single fiber state, but when dispersed in the molded body while several to several tens of fibers are converged, a large resistance is intermittently exhibited, and smooth cutting is difficult. become. Further, if cutting is further forced, there is a high possibility that the hardened tissue around the converged glass fiber will be destroyed. Further, the fine glass fibers having a diameter of 4 μm or less used in this molded body are partly powdered and float in the dust generated during processing, which deteriorates the working environment. It is feared that the pulverized glass fiber may adhere to workers, cause itch associated with it, and may cause skin diseases, which may affect the human body. Further, as with asbestos, there is a view that it affects lung function, and it is not acceptable as an industrial product for cutting and processing applications.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記の事情
に鑑み、木材系材料の代替材料として、セルロース系繊
維と無機質フィラー及び熱硬化性樹脂からなる複合板、
特に面材の有無に拘わらず石膏ボード廃材を有効利用し
てなる、軽量で強度に優れかつ良好な加工性(鋸作業性
及びドリル孔空け性等の切削性、釘打ち性)を有する複
合板及びその製造方法を提供することを目的としてなさ
れたものである。SUMMARY OF THE INVENTION In view of the above circumstances, the present invention provides, as an alternative material to a wood-based material, a composite plate composed of a cellulosic fiber, an inorganic filler and a thermosetting resin,
A composite plate that is made of waste gypsum board, whether or not it has a face material, and that is lightweight, has excellent strength, and has good workability (saw workability, machinability such as drilling, and nailing). And to provide a method for manufacturing the same.
【0006】[0006]
【課題を解決するための手段】上記の課題を解決するた
めに、本発明は、セルロース系繊維が15〜80重量
%、無機質フィラーが5〜40重量%及び熱硬化性樹脂
が10〜45重量%からなる配合体を加熱加圧して得ら
れる硬化成形体又はその接合体で、セルロース系繊維の
総表面積Spに対する無機質フィラーの総表面積Sfの
比(Sf/Sp)が0.05〜10.0であることを特徴
とする複合板を提供するものである。本発明はまた、セ
ルロース系繊維、無機質フィラー、熱硬化性樹脂及び水
からなるスラリーを調製する工程(ここで、該セルロー
ス系繊維の総表面積Spに対する該無機質フィラーの総
表面積Sfの比(Sf/Sp)は0.05〜10.0であ
る)、該スラリーを抄造して得られる湿潤成形体を乾燥
させて硬化性成形体を調製する工程、および 該硬化性
成形体を単数で又は複数枚積層後加熱加圧して硬化成形
体又はその接合体を調製する工程とを含む、前記の複合
板の製造方法を提供するものである。以下に本発明を詳
細に説明する。In order to solve the above-mentioned problems, the present invention provides a cellulosic fiber of 15 to 80% by weight, an inorganic filler of 5 to 40% by weight, and a thermosetting resin of 10 to 45% by weight. % Of the total surface area Sp of the cellulosic fiber (Sf / Sp) in a cured molded article or a joined body obtained by heating and pressing a blended body of 0.05 to 10.0. The present invention provides a composite plate characterized by the following. The present invention also provides a step of preparing a slurry composed of a cellulosic fiber, an inorganic filler, a thermosetting resin and water (wherein the ratio of the total surface area Sf of the inorganic filler to the total surface area Sp of the cellulosic fiber (Sf / Sp) is from 0.05 to 10.0), a step of preparing a curable molded article by drying a wet molded article obtained by forming the slurry, and a single or a plurality of the curable molded article. A method of manufacturing the above composite plate, which comprises a step of heating and pressing after lamination to prepare a cured molded article or a joined body thereof. Hereinafter, the present invention will be described in detail.
【0007】[0007]
【発明の実施の形態】本発明において使用されるセルロ
ース系繊維は、複合板に木質感、強度及び加工性を付与
すべく機能するものであり、かかるセルロース系繊維の
好ましい例としては、木材パルプ、リンターパルプ、麻
パルプ、藁パルプ、綿パルプ等に代表されるパルプ類及
びパルプ屑や、新聞紙、雑誌、電話帳、段ボール紙等に
代表される植物繊維系古紙由来の繊維などが挙げられる
が、これらに限定されるものではない。これらは1種用
いてもよく2種以上を組み合わせて用いてもよい。BEST MODE FOR CARRYING OUT THE INVENTION The cellulosic fiber used in the present invention functions to impart wood texture, strength and processability to a composite board. Preferred examples of the cellulosic fiber include wood pulp. , Linter pulp, hemp pulp, straw pulp, cotton pulp, and other pulps and pulp scraps, and fibers derived from plant fiber-based waste paper, such as newspaper, magazines, telephone directories, and corrugated cardboard. However, the present invention is not limited to these. These may be used alone or in combination of two or more.
【0008】本発明において使用される無機質フィラー
は、前記セルロース系繊維との組合せにより複合板の加
工性(特に切削性)の向上を果たすものであり、このよ
うな無機質フィラーとしては、炭酸カルシウム、シリカ
粉、カオリン、クレイ、酸化チタン、硫酸バリウム、石
膏、水酸化アルミニウム、タルク、マイカ、ガラスフレ
ーク、ハイドロサルタイト、ワラストナイト、チタン酸
カリウム、塩基性硫酸マグネシウム、セピオライト、ゾ
ノトライト、ホウ酸アルミニウム、パーライト、シラス
バルーン、廃ガラス発泡体、フライアッシュの他、石膏
ボード廃材粉砕物、高炉スラグ粉砕物、廃ガラス粉砕物
などが例示されるがこれらに限定されるものではない。
なお、ここでいう「石膏ボード廃材粉砕物」とは、石膏
ボードの生産から流通そして工事現場に至る過程で発生
する不良品、ロス品及び使用済み品等の石膏ボード廃材
を繊維質面材の有無に関係なく適当な粉砕機で粉砕し必
要に応じて分級処理して得られた粉末を意味する。The inorganic filler used in the present invention improves the workability (particularly the machinability) of the composite plate by combining it with the above-mentioned cellulosic fibers. Examples of such an inorganic filler include calcium carbonate, Silica powder, kaolin, clay, titanium oxide, barium sulfate, gypsum, aluminum hydroxide, talc, mica, glass flakes, hydrosaltite, wollastonite, potassium titanate, basic magnesium sulfate, sepiolite, xonotlite, aluminum borate In addition to perlite, shirasu balloon, waste glass foam and fly ash, crushed gypsum board waste material, crushed blast furnace slag, crushed waste glass, etc. are exemplified, but not limited thereto.
The term "crushed gypsum board waste material" used here refers to the waste of gypsum board such as defective products, lost products and used products that occur during the process from production of gypsum board to distribution and the construction site. Regardless of the presence or absence, it means a powder obtained by pulverizing with a suitable pulverizer and classifying if necessary.
【0009】このような無機質フィラーのなかでも、加
工機具の機械刃摩耗軽減のほか、加工性への寄与の点か
ら、モース硬度が5以下、好ましくは1〜5の無機質フ
ィラーが好適に用いられる。このような無機質フィラー
の例としては、例えば炭酸カルシウム、カオリン、クレ
イ、硫酸バリウム、石膏、タルク、マイカ、ハイドロサ
ルタイト、ワラストナイト、チタン酸カリウム、塩基性
硫酸マグネシウム、セピオライト、ゾノトライト、石膏
ボード廃材粉砕物などが挙げられる。中でも石膏ボード
廃材粉砕物は、廃材の再資源化という社会的なニーズに
も合致し、コストも安く、難燃性の付与機能の点でも特
に好ましいものである。これらの無機質フィラーは1種
用いてもよく、また2種以上を組み合わせて用いてもよ
い。また、かかる無機質フィラーは、粗大粒子の混在に
よる強度低下や表面平滑性の悪化を回避するため、好ま
しくは0.3mm以下の粒子径に調整して用いられる。Among these inorganic fillers, those having a Mohs hardness of 5 or less, preferably 1 to 5, are preferably used from the viewpoints of reducing the mechanical blade wear of the processing machine and contributing to the workability. . Examples of such inorganic fillers include, for example, calcium carbonate, kaolin, clay, barium sulfate, gypsum, talc, mica, hydrosaltite, wollastonite, potassium titanate, basic magnesium sulfate, sepiolite, xonotlite, gypsum board. Examples include crushed waste materials. Among them, the gypsum board waste material pulverized product is particularly preferable from the viewpoints of meeting the social needs of recycling the waste material, low cost, and the function of imparting flame retardancy. These inorganic fillers may be used alone or in combination of two or more. Further, such an inorganic filler is preferably adjusted to a particle diameter of 0.3 mm or less in order to avoid strength reduction and surface smoothness deterioration due to the inclusion of coarse particles.
【0010】本発明において使用される熱硬化性樹脂
は、架橋剤の存在下又は非存在下で熱硬化して、セルロ
ース系繊維及び無機質フィラー等を結合保持する結合機
能を有するものであり、このような熱硬化性樹脂の例と
しては、フェノール樹脂、エポキシ樹脂、不飽和ポリエ
ステル樹脂、メラミン樹脂、尿素樹脂などが挙げられ
る。中でも耐熱性、耐燃性及び剛性に優れるフェノール
樹脂が好ましい。これらは1種で用いてもよく、2種以
上を組み合わせてもよい。熱硬化性樹脂は、通常、粉末
状ないし繊維状固体で使用されるが、必要に応じて溶液
や樹脂液で又は固液組み合わせで用いられる。The thermosetting resin used in the present invention has a binding function of binding and holding the cellulosic fibers and the inorganic filler by thermosetting in the presence or absence of a crosslinking agent. Examples of such thermosetting resins include phenol resins, epoxy resins, unsaturated polyester resins, melamine resins, urea resins and the like. Above all, a phenol resin having excellent heat resistance, flame resistance and rigidity is preferable. These may be used alone or in combination of two or more. The thermosetting resin is usually used in the form of powder or fibrous solid, but if necessary, it may be used in the form of a solution, a resin liquid, or a solid-liquid combination.
【0011】ここでいうフェノール樹脂は、フェノール
類とアルデヒド類との縮合生成物又はその変性物で、硬
化剤の存在下又は非存在下で熱硬化してセルロース系繊
維や無機質フィラーを結合保持する結合剤機能を有する
ものであり、かかる熱硬化性フェノール樹脂としては、
ノボラック型フェノール樹脂、メチロール基含有ノボラ
ック型フェノール樹脂、アルカリレゾール型フェノール
樹脂、アンモニアレゾール型フェノール樹脂、ベンジリ
ックエーテル型フェノール樹脂等があげられる。さらに
また、これらのフェノール樹脂とエポキシ系化合物、キ
シレン系化合物、メラミン系化合物、尿素系化合物、ア
クリル系化合物、酢酸ビニール系化合物等の熱硬化性も
しくは熱可塑性化合物とを混合あるいは反応させて得ら
れる変性フェノール樹脂等が例示される。これらは1種
用いてもよく2種以上を組み合わせて用いてもよい。な
お、ノボラック型フェノール樹脂の単独使用においては
例えばヘキサメチレンテトラミンのような架橋性硬化剤
を用いて熱硬化性を付与する必要がある。The phenolic resin as used herein is a condensation product of phenols and aldehydes or a modified product thereof and is heat-cured in the presence or absence of a curing agent to bond and retain cellulosic fibers and inorganic fillers. As the thermosetting phenolic resin, which has a binder function,
Examples thereof include novolac type phenol resin, methylol group-containing novolac type phenol resin, alkali resol type phenol resin, ammonia resol type phenol resin, and benzylic ether type phenol resin. Furthermore, it is obtained by mixing or reacting these phenolic resins with a thermosetting or thermoplastic compound such as an epoxy compound, a xylene compound, a melamine compound, a urea compound, an acrylic compound, a vinyl acetate compound. Examples include modified phenolic resins. These may be used alone or in combination of two or more. When the novolac type phenol resin is used alone, it is necessary to impart thermosetting property by using a crosslinkable curing agent such as hexamethylenetetramine.
【0012】このような熱硬化性フェノール樹脂のなか
でも、メチロール基含有ノボラック型、アルカリレゾー
ル型、アンモニアレゾール型及びベンジリックエーテル
型フェノール樹脂は、複合板の臭気及び製造簡便さの点
で架橋性硬化剤を併用しなければならないノボラック型
フェノール樹脂より有利である。とりわけベンジリック
エーテル型フェノール樹脂は、他の樹脂より優れた熱安
定性及び着色安定性を有し、後述の湿潤成形体乾燥時の
変質を抑制できることから好適に用いられる。なお、熱
硬化性フェノール樹脂の使用形態は特に限定されない
が、一般的には粉末状ないし繊維状固体で必要に応じて
溶液や樹脂液で又は固液併用で用いられる。Among such thermosetting phenolic resins, the methylol group-containing novolac type, alkali resol type, ammonia resol type and benzylic ether type phenolic resins are crosslinkable in terms of odor of the composite plate and ease of production. It is more advantageous than the novolac type phenolic resin which must use a curing agent together. In particular, the benzylic ether type phenol resin is preferably used because it has heat stability and color stability superior to those of other resins and can suppress deterioration of the wet molded body described later when it is dried. The form of use of the thermosetting phenolic resin is not particularly limited, but it is generally a powdery or fibrous solid, and is used as a solution or a resin liquid or in combination with solid-liquid as required.
【0013】本発明に係る複合板は、前述したセルロー
ス系繊維を15〜80重量%、好ましくは30〜60重
量%、無機質フィラーを5〜40重量%、好ましくは2
0〜40重量%及び熱硬化性樹脂を10〜45重量%、
好ましくは20〜40重量%の範囲でそれぞれ調整配合
することにより製造される。セルロース系繊維の配合量
が15重量%未満又は80重量%を越えると、目標の加
工性又は強度を確保することが困難となる。また、無機
質フィラーの配合量が5重量%未満では加工性の改善効
果が十分でなく、逆に40重量%を越えると強度が悪化
して好ましくない。また、熱硬化性樹脂の配合量が10
重量%未満では目標の強度及び加工性を確保することが
困難であり、逆に45重量%を越えると強度は優れるも
のの加工性が悪化して好ましくない。The composite board according to the present invention contains the above-mentioned cellulosic fibers in an amount of 15 to 80% by weight, preferably 30 to 60% by weight, and an inorganic filler in an amount of 5 to 40% by weight, preferably 2%.
0-40% by weight and thermosetting resin 10-45% by weight,
It is preferably produced by adjusting and compounding each in the range of 20 to 40% by weight. If the blending amount of the cellulosic fiber is less than 15% by weight or exceeds 80% by weight, it becomes difficult to secure the target workability or strength. If the content of the inorganic filler is less than 5% by weight, the workability-improving effect is insufficient, and if it exceeds 40% by weight, the strength is deteriorated, which is not preferable. Further, the blending amount of the thermosetting resin is 10
If it is less than wt%, it is difficult to secure the target strength and workability. On the contrary, if it exceeds 45 wt%, the strength is excellent but the workability is deteriorated, which is not preferable.
【0014】さらに本発明に係る複合板においては、無
機質フィラーがセルロース系繊維の絡まり間隔中に充填
及び/又は繊維表面に付着した形の複合構造を形成して
いるため、熱硬化性樹脂による繊維相互の結合や繊維自
体の剛性化に伴う複合板の強度や硬度の増大が繊維単独
の複合板より緩和される。その結果、木材系材料に匹敵
する加工性(切削性及び釘打ち性)が付与され代替材料
として実用に供し得る。このような効果は、セルロース
系繊維の総表面積Spに対する無機質フィラーの総表面
積Sfの比(Sf/Sp)を好ましくはSf/Sp=
0.05〜10.0、より好ましくは0.1〜7.5に保持
することにより達成される。総表面積の比(Sf/S
p)が0.05未満の場合には、釘打ち性が向上する反
面、切削加工時に摩擦による焼けや焦げを生じ易くな
る。一方、Sf/Spが10.0を越える場合には、加
工性、特に切削抵抗の軽減に寄与し、切削面が平滑にな
り、特別な仕上げ工程を不要にする反面、釘打ち時に亀
裂の発生や割れを生じ易くなる。Further, in the composite plate according to the present invention, since the inorganic filler is filled and / or adhered to the fiber surface in the intertwisted space of the cellulosic fiber, the fiber formed of the thermosetting resin is used. The increase in strength and hardness of the composite plate due to mutual bonding and the rigidity of the fiber itself is relaxed as compared with the composite plate of the fibers alone. As a result, workability (cuttability and nailability) comparable to that of a wood-based material is imparted, and the material can be put to practical use as a substitute material. In order to obtain such an effect, the ratio (Sf / Sp) of the total surface area Sf of the inorganic filler to the total surface area Sp of the cellulosic fiber is preferably Sf / Sp =.
It is achieved by holding at 0.05 to 10.0, more preferably 0.1 to 7.5. Ratio of total surface area (Sf / S
When p) is less than 0.05, nailing performance is improved, but burning or scorching due to friction during cutting is likely to occur. On the other hand, when Sf / Sp exceeds 10.0, it contributes to the reduction of workability, especially cutting resistance, and the cutting surface becomes smooth and no special finishing process is required, but cracks occur during nailing. And cracks easily occur.
【0015】また、前記Sf/Spは、本発明方法の抄
造時における重要な要素である濾水性及び歩留まり特性
のバランスに寄与することを知見した。すなわち、Sf
/Spが0.05未満の場合には、セルロース系繊維自
体の保水性及び無機質フィラーの流出抑制作用により歩
留まりは向上するが、濾水性の低下で生産効率の悪化を
招くことになる。一方、Sf/Spが10.0を越える
場合には、セルロース系繊維の前記作用の弱化により、
濾水性は向上するが歩留まりの低下を招くことになる。It was also found that the Sf / Sp contributes to the balance of drainage and retention characteristics, which are important factors during the papermaking of the method of the present invention. That is, Sf
When / Sp is less than 0.05, the yield is improved due to the water retention of the cellulosic fiber itself and the outflow suppressing effect of the inorganic filler, but the drainage is lowered and the production efficiency is deteriorated. On the other hand, when Sf / Sp exceeds 10.0, the weakening of the above action of the cellulosic fiber causes
The drainage is improved but the yield is reduced.
【0016】このような複合板は、下記の抄造法を適用
した方法により好適に製造することができるがこれに限
定されるものではない。先ず、予め多量の水が投入され
ている離解叩解機(例えばパルパー、ヘンシェルミキサ
ー)内にセルロース系繊維、無機質フィラー及び熱硬化
性樹脂を投入した後、高速撹拌により繊維の離解と共に
各成分の分散混合を図り、必要に応じてさらに撹拌翼付
混合槽で混合してセルロース系繊維、無機質フィラー、
熱硬化性樹脂及び水からなるスラリーを作る。この際ス
ラリー濃度(固形分)は、後記の抄造工程における抄造
作業に応じて適当に調整されるが、一般的には0.01
〜10重量%である。本発明方法では、このような低ス
ラリー濃度を採用するため、繊維質面材付き石膏ボード
廃材粉砕物を従来の石膏ボード製法より多量に使用する
ことができるという利点を有する。また、比較的水溶性
の大きな無機質フィラー、例えば石膏ボード粉砕物を使
用する場合には、水への無機質フィラーの溶出による配
合物の歩留まり低下を回避するため、水の代替として該
無機質フィラーの飽和水溶液又は過飽和水溶液の使用が
推奨される。Such a composite plate can be suitably manufactured by a method applying the following papermaking method, but the invention is not limited thereto. First, after introducing cellulosic fibers, inorganic filler and thermosetting resin into a disintegrating beater (for example, pulper, Henschel mixer) in which a large amount of water has been added in advance, disperse each component together with disaggregation of the fibers by high speed stirring. For mixing, cellulosic fiber, inorganic filler, and further mixed in a mixing tank with stirring blades if necessary.
Make a slurry of thermosetting resin and water. At this time, the slurry concentration (solid content) is appropriately adjusted according to the papermaking operation in the papermaking process described later, but generally 0.01
10 to 10% by weight. Since the method of the present invention employs such a low slurry concentration, it has an advantage that a large amount of the pulverized gypsum board waste material with a fibrous surface material can be used as compared with the conventional gypsum board manufacturing method. Further, in the case of using a relatively water-soluble large inorganic filler, for example, gypsum board crushed product, in order to avoid a decrease in the yield of the formulation due to the elution of the inorganic filler into water, saturation of the inorganic filler as a substitute for water. The use of aqueous or supersaturated aqueous solutions is recommended.
【0017】次に、前記工程で得られたスラリーに対
し、好ましくは定着剤を加えて混合した後、これを例え
ば長網型ないし円筒型の連続式又はバッチ式抄造機によ
り所望形状、例えばシート状ないし薄板状の湿潤成形体
に抄造し、濾過、減圧、圧搾等により脱水し、乾燥装
置、例えばドラム乾燥機、熱風通気乾燥機、誘電加熱乾
燥機、遠赤外線乾燥機、減圧乾燥機等で乾燥させて未硬
化状態の硬化性成形体を得る。なお、前記抄造工程で作
製された湿潤成形体には必要に応じて架橋性硬化剤(例
えばヘキサメチレンテトラミンや水溶性レゾール型フェ
ノール樹脂)、硬化促進剤等を例えばスプレー含浸によ
り定着させてもよい。又、かかる硬化性成形体の製作に
は、場合によっては、適当な粉砕機で粉砕ないし離解処
理した、セルロース系繊維、無機質フィラー、熱硬化性
樹脂をミキサーにより均一に混合して得られた混合物
を、例えばフリース製造機等の賦形機により所望坪量の
マット状フリースに賦形し、これを焼成機やプレス機等
により樹脂の硬化を抑制しつつ所望厚み(例えばシート
状、薄板状、マット状)に調整して未硬化状態の硬化性
成形体を得る乾式法を採用してもよい。Next, a fixing agent is preferably added to and mixed with the slurry obtained in the above step, and the mixture is mixed with a desired shape, for example, a sheet by a fourdrinier or cylindrical continuous or batch papermaking machine. Paper into a sheet-shaped or thin plate-shaped wet molded body, dehydrated by filtration, decompression, pressing, etc., and dried with a drying device such as a drum dryer, a hot air ventilation dryer, a dielectric heating dryer, a far infrared dryer, a vacuum dryer, etc. It is dried to obtain an uncured curable molded body. If necessary, a crosslinkable curing agent (for example, hexamethylenetetramine or a water-soluble resol-type phenol resin), a curing accelerator, etc. may be fixed to the wet molded article produced in the papermaking step by spray impregnation. . In addition, in order to produce such a curable molded article, a mixture obtained by uniformly mixing a cellulosic fiber, an inorganic filler, and a thermosetting resin, which have been pulverized or disaggregated by an appropriate pulverizer, with a mixer in some cases. Is shaped into a mat-shaped fleece having a desired basis weight with a shaping machine such as a fleece manufacturing machine, and a desired thickness (for example, sheet shape, thin plate shape, while suppressing curing of the resin with a baking machine, a press machine, or the like). A dry method may be employed in which a curable molded body in an uncured state is obtained by adjusting the matte type).
【0018】次に、上記工程で得られた硬化性成形体
は、単数で又は複数積層後、加熱加圧機構を有する成形
機、例えば圧縮成形機、引き抜き成形機、押出機等で硬
化させることにより単層又は積層構造の複合板(硬化成
形体)に形成される。また、前記単層又は積層構造の硬
化成形体は、さらに例えばネジ、クギ、接着剤等の接合
固定化手段、好ましくは接着剤、とりわけ硬化型接着
剤、例えばフェノール樹脂、尿素樹脂、メラミン樹脂、
エポキシ樹脂、ウレタン樹脂等により部分若しくは全面
接着固定した積層構造の複合板(接合体)にすることも
できる。Next, the curable molded product obtained in the above step is singly or plurally laminated and then cured by a molding machine having a heating and pressing mechanism, for example, a compression molding machine, a pultrusion molding machine, an extruder or the like. To form a composite plate (cured molded product) having a single-layer or laminated structure. Further, the cured molded body of the single layer or laminated structure, further, for example, screws, nails, bonding and fixing means such as adhesives, preferably adhesives, especially curable adhesives such as phenolic resin, urea resin, melamine resin,
It is also possible to form a composite plate (joint body) having a laminated structure in which a part or the whole surface is adhesively fixed with an epoxy resin, a urethane resin or the like.
【0019】本発明方法における前記スラリー調製工程
では、必要に応じて各種添加物、例えば架橋性硬化剤、
硬化促進剤、水溶性ポリマー等の糊剤、界面活性剤(分
散剤や消泡剤)、紙力補強剤の他、本発明の要旨を阻害
しない範囲で、適当な強化繊維類、例えばアラミド繊
維、ナイロン繊維、ポリエステル繊維、硬化フェノール
繊維、炭素繊維、アルミニウム繊維等を配合してもよ
い。また、本発明複合板の表裏面及び/又は中芯部に
は、必要に応じてメラミン樹脂化粧紙、ジアリルフタレ
ート樹脂化粧紙等の樹脂含浸化粧紙類、クラフト紙、ア
ルミクラフト紙、プリント紙等の紙類、アクリル樹脂、
塩化ビニール樹脂等のプラスチックシート類、コルクシ
ート、天然木ツキ板等の木質系薄板類、アルミニウム薄
板、ステンレス薄板、エンボス加工金属薄板等の金属系
薄板類、無機質繊維又は有機質繊維の織布又は不織布な
どを設けてもよい。In the slurry preparing step in the method of the present invention, various additives such as a crosslinkable curing agent, if necessary,
A curing accelerator, a sizing agent such as a water-soluble polymer, a surfactant (dispersing agent or defoaming agent), a paper-strengthening agent, and other suitable reinforcing fibers such as aramid fiber within the scope of the present invention. , Nylon fiber, polyester fiber, cured phenol fiber, carbon fiber, aluminum fiber and the like may be blended. Further, on the front and back surfaces and / or the core of the composite plate of the present invention, resin impregnated decorative papers such as melamine resin decorative paper and diallyl phthalate resin decorative paper, kraft paper, aluminum kraft paper, printed paper, etc. Paper, acrylic resin,
Plastic sheets such as vinyl chloride resin, cork sheets, wood-based thin plates such as natural wood plywood, aluminum thin plates, stainless steel thin plates, metal thin plates such as embossed metal thin plates, woven or non-woven fabric of inorganic fibers or organic fibers Etc. may be provided.
【0020】かくして得られた本発明に係る複合板は、
木材系材料の代替適用を主目的としているため、好まし
くは、密度は500〜900kg/m3、好ましくは6
00〜800kg/m3、曲げ強度は200kg/cm2
以上、好ましくは200〜700kg/cm2、より好
ましくは300〜500kg/cm2を有する必要があ
る。密度が500kg/cm3未満では目標の強度及び
加工性の確保が困難であり、逆に900kg/cm3を
越すと重過ぎるし加工性も悪化して好ましくない。ま
た、曲げ強度が200kg/cm2未満では代替材料と
して実用に供し得ない。The composite plate according to the present invention thus obtained is
Since the main purpose is to substitute the wood-based material, the density is preferably 500 to 900 kg / m 3 , preferably 6
00-800 kg / m 3 , bending strength is 200 kg / cm 2
It is necessary to have the above, preferably 200 to 700 kg / cm 2 , and more preferably 300 to 500 kg / cm 2 . If the density is less than 500 kg / cm 3, it is difficult to secure the target strength and workability, while if it exceeds 900 kg / cm 3 , it is too heavy and the workability deteriorates, which is not preferable. If the bending strength is less than 200 kg / cm 2 , it cannot be put to practical use as a substitute material.
【0021】[0021]
【実施例】以下、本発明を実施例により具体的に説明す
るが、本発明はこれらの実施例によって限定されるもの
ではない。なお、本発明において採用した試験方法はそ
れぞれ次のとおりである。 (i) 複合板の密度:JIS Z−2117による。 (ii) 曲げ強度:JIS K−6911による。 (iii) 無機質フィラー及びセルロース系繊維の比表面
積:BET法による。また、セルロース系繊維の総表面
積Spに対する無機質フィラーの総表面積Sfの比(S
f/Sp)は、それぞれ比表面積値に使用量を乗じて算
出した。 (iV) 切削性:ルーターで次の条件により溝加工を施し
た。 切削刃回転数:3000rpm、切削速度20mm/
秒、切削幅10mm、切削深さ5mm、切削長さ200
mm。 評価項目:切削面の焼け、変色、切削溝角面の欠損の有
無等を総合的に観察した。 (V) 釘打ち性:胴部径2.45mm、長さ45mmの鉄
製釘(JIS A5508のN45に相当)を、次の条
件で手でハンマー打ちした。 釘打ち箇所:表裏それぞれについて、面端部から5mm
内側に15mm間隔で5本。両側面それぞれについて、
板厚みの中心に20mm間隔で3本。 評価項目:釘打ち抵抗(釘の屈曲程度)、釘間の亀裂
(表裏)、釘周辺の亀裂(表裏)、板厚みの変化等を総
合的に観察した。 (Vi) 評価の表示:比較のために使用した合板(日本農
林規格規定の普通合板)を基準に、上記切削性及び釘打
ち性を評価し、優れている場合を「◎」、同等程度の場
合は「○」、やや劣るが実用上支障のない場合は
「△」、実用に供し得ない程度に劣る場合は「×」で表
示した。EXAMPLES Hereinafter, the present invention will be described specifically with reference to examples, but the present invention is not limited to these examples. The test methods adopted in the present invention are as follows. (i) Density of composite plate: According to JIS Z-2117. (ii) Bending strength: According to JIS K-6911. (iii) Specific surface area of inorganic filler and cellulosic fiber: According to BET method. Further, the ratio of the total surface area Sf of the inorganic filler to the total surface area Sp of the cellulosic fiber (S
f / Sp) was calculated by multiplying the specific surface area value by the amount used. (iV) Machinability: Grooving was performed on the router under the following conditions. Cutting blade rotation speed: 3000 rpm, cutting speed 20 mm /
Seconds, cutting width 10 mm, cutting depth 5 mm, cutting length 200
mm. Evaluation items: Burning of the cutting surface, discoloration, and the presence or absence of defects in the cutting groove corner surface were comprehensively observed. (V) Nailability: An iron nail (corresponding to N45 of JIS A5508) having a body diameter of 2.45 mm and a length of 45 mm was hammered by hand under the following conditions. Nailed location: 5mm from the edge of the front and back
Five inside with 15mm intervals. For each side,
Three at 20 mm intervals in the center of the plate thickness. Evaluation items: Nail driving resistance (bending degree of nails), cracks between nails (front and back), cracks around nails (front and back), changes in plate thickness, etc. were comprehensively observed. (Vi) Display of evaluation: Based on the plywood used for comparison (ordinary plywood defined by the Japan Agriculture and Forestry Standard), the above-mentioned machinability and nailability were evaluated. If excellent, "◎", equivalent The case was indicated by "○", the case where it was slightly inferior, but there was no problem in practical use, was indicated by "△", and the case where it was inferior to the extent that it could not be put to practical use was indicated by "X".
【0022】(実施例1)ヘンシェルミキサー内に水4
kgと針葉樹クラフトパルプ(比表面積0.7m2/g)
25gを投入して120秒間撹拌離解し、次に炭酸カル
シウム(比表面積1.1m2/g、モース硬度3)10g
とベンジリックエーテル型フェノール樹脂粉末15gを
追加し、更に60秒間撹拌混合してスラリーを得た。な
お、Sf/Spの比は0.63であった。引き続き、こ
のスラリーにポリアクリルアミド系定着剤を加えて撹拌
混合した後、これを東洋精機製標準角型シートマシン
(実験用抄造機、抄造網100メッシュ、250mm×
200mm)に全量注入し、濾過し、更に吸引圧搾脱水
を行って湿潤状態の成形体を得た。次いで、この湿潤成
形体を80℃の熱風通気乾燥機内で乾燥して硬化性成形
体を得た。次いで、高さ10mmの金枠内に前記同様に
して作製した硬化性成形体8枚を積層載置した後、これ
を温度180℃で15分間加熱加圧成形して複合板を得
た。Example 1 Water 4 in a Henschel mixer
kg and softwood kraft pulp (specific surface area 0.7 m 2 / g)
25 g was added, and the mixture was stirred and disintegrated for 120 seconds, and then 10 g of calcium carbonate (specific surface area 1.1 m 2 / g, Mohs hardness 3)
And 15 g of benzylic ether type phenol resin powder were added, and the mixture was further stirred and mixed for 60 seconds to obtain a slurry. The Sf / Sp ratio was 0.63. Subsequently, a polyacrylamide-based fixing agent was added to this slurry with stirring and mixing, and this was then standard square sheet machine made by Toyo Seiki (experimental papermaking machine, papermaking mesh 100 mesh, 250 mm ×
(200 mm), the whole amount was injected, the mixture was filtered, and suction press dehydration was performed to obtain a wet molded body. Next, this wet molded body was dried in a hot air ventilation dryer at 80 ° C. to obtain a curable molded body. Next, eight curable moldings produced in the same manner as described above were stacked and placed in a metal frame having a height of 10 mm, and this was heated and pressed at 180 ° C. for 15 minutes to obtain a composite plate.
【0023】(実施例2)実施例1において、炭酸カル
シウムに代えてタルク(比表面積2.5m2/g、モース
硬度1)10gを使用した以外は実施例1と同様にして
複合板を得た。なお、Sf/Spの比は1.4であっ
た。(Example 2) A composite plate was obtained in the same manner as in Example 1 except that 10 g of talc (specific surface area 2.5 m 2 / g, Mohs hardness 1) was used in place of calcium carbonate. It was The Sf / Sp ratio was 1.4.
【0024】(実施例3)実施例1において、炭酸カル
シウムに代えてワラストナイト(比表面積0.78m2/
g、モース硬度4.5)10gを使用した以外は実施例
1と同様にして複合板を得た。なお、Sf/Spの比は
0.45であった。(Example 3) In Example 1, instead of calcium carbonate, wollastonite (specific surface area 0.78 m 2 /
g, Mohs hardness 4.5) A composite plate was obtained in the same manner as in Example 1 except that 10 g was used. The Sf / Sp ratio was 0.45.
【0025】(実施例4)実施例1において、炭酸カル
シウムに代えて水酸化アルミニウム(比表面積8m2/
g、モース硬度3)10gを使用した以外は実施例1と
同様にして複合板を得た。なお、Sf/Spの比は4.
5であった。Example 4 In Example 1, instead of calcium carbonate, aluminum hydroxide (specific surface area 8 m 2 /
g, Mohs hardness 3) A composite plate was obtained in the same manner as in Example 1 except that 10 g was used. The Sf / Sp ratio is 4.
It was 5.
【0026】(実施例5)実施例1において、炭酸カル
シウムに代えて超微細炭酸カルシウム(比表面積11.
5m2/g、モース硬度3)10gを使用した以外は実
施例1と同様にして複合板を得た。なお、Sf/Spの
比は6.6であった。(Example 5) In Example 1, instead of calcium carbonate, ultrafine calcium carbonate (specific surface area 11.
A composite plate was obtained in the same manner as in Example 1 except that 5 m 2 / g and Mohs hardness 3) 10 g were used. The Sf / Sp ratio was 6.6.
【0027】(実施例6)ヘンシェルミキサー内に二水
石膏飽和水4kgと実施例1で使用した針葉樹クラフト
パルプ25gを投入して120秒間撹拌離解し、次に紙
面材由来の繊維分1.5重量%を含む二水石膏主体の石
膏ボード廃材粉砕物(比表面積1.9m2/g、モース硬
度2)10gとベンジリックエーテル型フェノール樹脂
粉末15gを追加し、更に60秒間撹拌混合してスラリ
ーを得た。なお、Sf/Spの比は1.1であった。引
き続き、このスラリーにポリアクリルアミド系定着剤を
加えて撹拌混合した後、これを東洋精機製標準角型シー
トマシン(実験用抄造機、抄造網100メッシュ、25
0mm×200mm)全量注入し、濾過し、更に吸引圧
搾脱水を行って湿潤状態の成形体を得た。次いで、この
湿潤成形体を80℃の熱風通気乾燥機内で乾燥して硬化
性成形体を得た。なお、得られた硬化性成形体の歩留ま
りは、総仕込み量に対して93重量%であったが、二水
石膏飽和水に代えて水を用いた場合の歩留まりは75重
量%であった。次いで、高さ10mmの金枠内に前記同
様に作製した硬化性成形体8枚を積層載置した後、これ
を温度180℃で15分間加熱加圧成形して複合板を得
た。Example 6 4 kg of saturated water of gypsum dihydrate and 25 g of the softwood kraft pulp used in Example 1 were put into a Henschel mixer, stirred and disintegrated for 120 seconds, and then a fiber component derived from a paper surface material of 1.5 Add 10 g of pulverized gypsum board waste material mainly containing dihydrate gypsum (specific surface area 1.9 m 2 / g, Mohs hardness 2) containing 15% by weight and 15 g of benzylic ether type phenol resin powder, and stir and mix for 60 seconds to form a slurry. Got The Sf / Sp ratio was 1.1. Subsequently, a polyacrylamide-based fixing agent was added to this slurry, and the mixture was stirred and mixed, and this was then standard square sheet machine (laboratory papermaking machine, papermaking mesh 100 mesh, 25
(0 mm × 200 mm), the whole amount was injected, filtered, and suction-pressed and dehydrated to obtain a molded product in a wet state. Next, this wet molded body was dried in a hot air ventilation dryer at 80 ° C. to obtain a curable molded body. The yield of the obtained curable molded product was 93% by weight with respect to the total amount charged, but the yield was 75% by weight when water was used instead of the gypsum dihydrate saturated water. Next, eight curable molded bodies produced in the same manner as described above were stacked and placed in a metal frame having a height of 10 mm, and then heat-press molded at a temperature of 180 ° C. for 15 minutes to obtain a composite plate.
【0028】(実施例7)実施例6において、針葉樹ク
ラフトパルプに代えて新聞古紙パルプ(比表面積2.7
m2/g)25gを使用した以外は実施例6と同様にし
て複合板を得た。なお、Sf/Spの比は0.28であ
った。(Example 7) In Example 6, instead of the softwood kraft pulp, recycled newspaper pulp (specific surface area 2.7
A composite plate was obtained in the same manner as in Example 6 except that 25 g of m 2 / g) was used. The Sf / Sp ratio was 0.28.
【0029】(比較例1)実施例1において、炭酸カル
シウムに代えて超微細炭酸カルシウム17.5gを使用
し、針葉樹クラフトパルプの使用量を17.5gに変更
した以外は実施例1と同様にして複合板を得た。なお、
Sf/Spの比は16.4であった。Comparative Example 1 The same as Example 1 except that 17.5 g of ultrafine calcium carbonate was used in place of calcium carbonate and the amount of softwood kraft pulp used was changed to 17.5 g. To obtain a composite board. In addition,
The Sf / Sp ratio was 16.4.
【0030】(比較例2)ヘンシェルミキサー内に水4
kgと実施例1で使用した針葉樹クラフトパルプ35g
を投入して120秒間撹拌離解し、次にベンジリックエ
ーテル型フェノール樹脂粉末15gを追加し、更に60
秒間撹拌混合してスラリーを得た。引き続き、このスラ
リーにポリアクリルアミド系定着剤を加えて撹拌混合し
た後、これを東洋精機製標準角型シートマシン(実験用
抄造機、抄造網100メッシュ、250mm×200m
m)に全量注入し、濾過し、更に吸引圧搾脱水を行って
湿潤状態の成形体を得た。次いで、この湿潤成形体を8
0℃の熱風通気乾燥機内で乾燥して硬化性成形体を得
た。次いで、高さ10mmの金枠内に前記同様にして作
製した硬化性成形体8枚を積層載置した後、これを温度
180℃で15分間加熱加圧成形して複合板を得た。(Comparative Example 2) Water 4 in a Henschel mixer
kg and 35 g of the softwood kraft pulp used in Example 1
Is added and stirred and disintegrated for 120 seconds, then 15 g of benzylic ether type phenol resin powder is added, and further 60
The mixture was stirred and mixed for 2 seconds to obtain a slurry. Subsequently, a polyacrylamide-based fixing agent was added to this slurry with stirring and mixing, and this was then standard square sheet machine manufactured by Toyo Seiki (experimental papermaking machine, papermaking mesh 100 mesh, 250 mm × 200 m).
The whole amount was poured into m), filtered, and further suction-pressed and dehydrated to obtain a wet molded body. Then, the wet molded body is
A curable molded body was obtained by drying in a hot air ventilation dryer at 0 ° C. Next, eight curable molded bodies produced in the same manner as described above were stacked and placed in a metal frame having a height of 10 mm, and then heat-press molded at a temperature of 180 ° C. for 15 minutes to obtain a composite plate.
【0031】(比較例3)実施例6において、針葉樹ク
ラフトパルプを5g、石膏ボード廃材粉砕物を40g、
ベンジリックエーテル型フェノール樹脂粉末を5gに変
更した以外は実施例6と同様にして硬化性成形体を作製
した、次いで、高さ10mmの金枠内に前記硬化性成形
体9枚を積層載置し、温度180℃で15分間加熱加圧
成形して複合板を得た。なお、Sf/Spの比は21.
7であった。(Comparative Example 3) In Example 6, 5 g of softwood kraft pulp, 40 g of ground gypsum board waste material,
A curable molded body was produced in the same manner as in Example 6 except that the amount of the benzylic ether type phenolic resin powder was changed to 5 g, and then 9 pieces of the curable molded body were stacked and placed in a metal frame having a height of 10 mm. Then, the composite plate was obtained by heat-press molding at a temperature of 180 ° C. for 15 minutes. The Sf / Sp ratio is 21.
It was 7.
【0032】(比較例4)実施例6において、針葉樹ク
ラフトパルプを15g、石膏ボード廃材粉砕物を7.5
g、ベンジリックエーテル型フェノール樹脂粉末を2
7.5gに変更した以外は実施例6と同様にして硬化性
成形体を作製した、次いで、高さ10mmの金枠内に前
記硬化性成形体8枚を積層載置し、温度180℃で15
分間加熱加圧成形して複合板を得た。なお、Sf/Sp
の比は1.4であった。Comparative Example 4 In Example 6, 15 g of softwood kraft pulp and 7.5 g of ground gypsum board waste material were used.
2 g of benzylic ether type phenol resin powder
A curable molded body was prepared in the same manner as in Example 6 except that the amount of the curable molded body was changed to 7.5 g. Then, 8 pieces of the curable molded body were stacked and placed in a metal frame having a height of 10 mm at a temperature of 180 ° C. 15
A composite plate was obtained by heat-press molding for minutes. In addition, Sf / Sp
The ratio was 1.4.
【0033】次に、前記実施例及び比較例で得た複合板
(実施例1〜7及び比較例1〜4)と本発明と対照比較
のため用いた合板(比較例5)については、冒頭記載の
試験方法により密度、曲げ強さ及び加工性(切削性及び
釘打ち性)について評価した。それらの結果を表1及び
表2に示す。Next, regarding the composite plates (Examples 1 to 7 and Comparative Examples 1 to 4) obtained in the above Examples and Comparative Examples and the plywood (Comparative Example 5) used for comparison between the present invention and the control, The density, bending strength and workability (cuttability and nailability) were evaluated by the test methods described. The results are shown in Tables 1 and 2.
【0034】[0034]
【表1】 [Table 1]
【0035】[0035]
【表2】 [Table 2]
【0036】[0036]
【発明の効果】以上詳しく説明したとおり、本発明に係
る複合板は、合板と遜色のない軽量さ、強度及び加工性
を有するため、木材系材料の代替材料として例えば建築
土木用部材、木工用部材、教材等に使用することができ
る。また、本発明方法によれば、低スラリー濃度の抄造
法を採用するため、従来廃棄処分されていた特に繊維質
面材付き石膏ボード廃材を有効に活用することができ
る。また抄造水として無機質フィラーの飽和もしくは過
飽和水溶液を用いると、品質の安定した複合板を高歩留
まりで製造することができる。さらには、抄造時の重要
な要素である濾水性及び歩留まりをバランスできるとい
う利点を提供できる。このように本発明によれば、産業
廃棄物である石膏ボード廃材を再利用してなる、木材系
材料の代替材料として実用可能な複合板を容易に提供で
きるため、社会的に注視されている石膏ボード廃材問題
の解決及び木材資源の節減による自然環境の保護に寄与
することができる。As described in detail above, the composite board according to the present invention has a weight, strength, and workability comparable to those of plywood. Therefore, as a substitute material for wood-based materials, for example, members for construction civil engineering and woodworking. It can be used for parts, teaching materials, etc. Further, according to the method of the present invention, since the papermaking method with a low slurry concentration is adopted, it is possible to effectively utilize the gypsum board waste material with the fibrous surface material, which has been conventionally discarded. When a saturated or supersaturated aqueous solution of an inorganic filler is used as the papermaking water, a composite plate with stable quality can be produced with a high yield. Furthermore, it is possible to provide the advantage that the drainage and the yield, which are important factors during papermaking, can be balanced. As described above, according to the present invention, it is possible to easily provide a composite board which is a waste material of gypsum board, which is an industrial waste, and which can be practically used as a substitute material for a wood-based material, and thus is paid attention to society. It can contribute to solving the problem of waste gypsum board and protecting the natural environment by saving wood resources.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 永田 憲史 千葉県佐倉市大作二丁目4番2号 秩父小 野田株式会社中央研究所内 (72)発明者 田島 勲 大阪府大阪市西区新町1丁目6番22号 双 和化成株式会社内 (72)発明者 長田 光巨 愛知県丹羽郡扶桑町大字南山名字新津26番 地の4 旭有機材工業株式会社愛知工場内 (72)発明者 甲斐 勲 愛知県丹羽郡扶桑町大字南山名字新津26番 地の4 旭有機材工業株式会社愛知工場内 (72)発明者 兼岩 敏彦 愛知県丹羽郡扶桑町大字南山名字新津26番 地の4 旭有機材工業株式会社愛知工場内 ─────────────────────────────────────────────────── ─── Continued Front Page (72) Inventor Kenji Nagata 2-4-2 Daisaku Sakura, Chiba Prefecture Chichibu Onoda Central Research Institute (72) Inventor Isao Tajima 1-6 Shinmachi, Nishi-ku, Osaka-shi, Osaka No. 22 Sowa Kasei Co., Ltd. (72) Inventor Mitsugi Nagata 4 Azai Organic Materials Co., Ltd. Aichi Plant, No. 26, Niitsu, Fuso-cho, Niwa-gun, Aichi Prefecture 4 Asahi Organic Material Industry Co., Ltd. 26, Niitsu 26, Minamiyama, Fuso-cho, Gunma (72) Inventor, Toshihiko Kaneiwa Toshihiko Iwa 4 4 Asahi Organic Material Co., Ltd., Niiyama, Fuso-cho, Niwa-gun, Aichi Prefecture Aichi factory
Claims (6)
無機質フィラーが5〜40重量%及び熱硬化性樹脂が1
0〜45重量%からなる配合体を加熱加圧して得られる
硬化成形体又はその接合体で、セルロース系繊維の総表
面積Spに対する無機質フィラーの総表面積Sfの比
(Sf/Sp)が0.05〜10.0であることを特徴と
する複合板。1. A cellulosic fiber is 15 to 80% by weight,
5-40% by weight of inorganic filler and 1% of thermosetting resin
A cured molded product obtained by heating and pressing a compounded body of 0 to 45% by weight or a bonded product thereof, and the ratio (Sf / Sp) of the total surface area Sf of the inorganic filler to the total surface area Sp of the cellulosic fiber is 0.05. A composite plate characterized by being in the range of 10.0.
のである請求項1に記載の複合板。2. The composite plate according to claim 1, wherein the inorganic filler has a Mohs hardness of 5 or less.
ボード廃材粉砕物である請求項1又は2に記載の複合
板。3. The composite board according to claim 1, wherein at least a part of the inorganic filler is a pulverized product of gypsum board waste material.
硬化性樹脂及び水からなるスラリーを調製する工程(こ
こで、該セルロース系繊維の総表面積Spに対する該無
機質フィラーの総表面積Sfの比(Sf/Sp)は0.
05〜10.0である)、 該スラリーを抄造して得られる湿潤成形体を乾燥させて
硬化性成形体を調製する工程、および該硬化性成形体を
単数で又は複数枚積層後加熱加圧して硬化成形体又はそ
の接合体を調製する工程とを含む、請求項1記載の複合
板の製造方法。4. A step of preparing a slurry composed of a cellulosic fiber, an inorganic filler, a thermosetting resin, and water (here, a ratio of a total surface area Sf of the inorganic filler to a total surface area Sp of the cellulosic fiber (Sf / Sp) is 0.
05-1.0), a step of preparing a curable molded article by drying a wet molded article obtained by forming the slurry into a sheet, and heating and pressurizing the curable molded article after laminating a single or plural curable molded articles. The manufacturing method of the composite board of Claim 1 including the process of preparing a hardening molded object or its joined body.
のである請求項4に記載の製造方法。5. The method according to claim 4, wherein the inorganic filler has a Mohs hardness of 5 or less.
石膏ボード廃材粉砕物を用いる、請求項4又は5に記載
の製造方法。6. The production method according to claim 4, wherein a crushed product of gypsum board waste material is used as at least a part of the inorganic filler.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP01615596A JP3478651B2 (en) | 1996-01-31 | 1996-01-31 | Composite plate and method of manufacturing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP01615596A JP3478651B2 (en) | 1996-01-31 | 1996-01-31 | Composite plate and method of manufacturing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH09209299A true JPH09209299A (en) | 1997-08-12 |
JP3478651B2 JP3478651B2 (en) | 2003-12-15 |
Family
ID=11908624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP01615596A Expired - Fee Related JP3478651B2 (en) | 1996-01-31 | 1996-01-31 | Composite plate and method of manufacturing the same |
Country Status (1)
Country | Link |
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JP (1) | JP3478651B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017128834A (en) * | 2016-01-22 | 2017-07-27 | 日本製紙株式会社 | Method for making paper |
-
1996
- 1996-01-31 JP JP01615596A patent/JP3478651B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017128834A (en) * | 2016-01-22 | 2017-07-27 | 日本製紙株式会社 | Method for making paper |
Also Published As
Publication number | Publication date |
---|---|
JP3478651B2 (en) | 2003-12-15 |
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