JPH0333840B2 - - Google Patents
Info
- Publication number
- JPH0333840B2 JPH0333840B2 JP58030791A JP3079183A JPH0333840B2 JP H0333840 B2 JPH0333840 B2 JP H0333840B2 JP 58030791 A JP58030791 A JP 58030791A JP 3079183 A JP3079183 A JP 3079183A JP H0333840 B2 JPH0333840 B2 JP H0333840B2
- Authority
- JP
- Japan
- Prior art keywords
- fiberboard
- fibers
- resins
- molded
- synthetic resin
- 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.)
- Expired - Lifetime
Links
- 239000000835 fiber Substances 0.000 claims description 40
- 239000011094 fiberboard Substances 0.000 claims description 32
- 229920003002 synthetic resin Polymers 0.000 claims description 22
- 239000000057 synthetic resin Substances 0.000 claims description 22
- 229920001169 thermoplastic Polymers 0.000 claims description 20
- 239000004416 thermosoftening plastic Substances 0.000 claims description 20
- 239000002775 capsule Substances 0.000 claims description 18
- 239000000126 substance Substances 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 238000004513 sizing Methods 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 239000002002 slurry Substances 0.000 claims description 6
- 238000007731 hot pressing Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 235000013311 vegetables Nutrition 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 19
- 239000011347 resin Substances 0.000 description 19
- 239000004088 foaming agent Substances 0.000 description 13
- 230000005484 gravity Effects 0.000 description 11
- 238000000465 moulding Methods 0.000 description 10
- 238000005187 foaming Methods 0.000 description 9
- 230000001070 adhesive effect Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000006260 foam Substances 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- -1 polyethylene Polymers 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 3
- 235000017491 Bambusa tulda Nutrition 0.000 description 3
- 241001330002 Bambuseae Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000011425 bamboo Substances 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N 2,2-dimethylbutane Chemical compound CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- UOYIYWCAYFTQLH-UHFFFAOYSA-N 3,7-dinitro-1,3,5,7-tetrazabicyclo[3.3.1]nonane Chemical compound C1N2CN([N+](=O)[O-])CN1CN([N+]([O-])=O)C2 UOYIYWCAYFTQLH-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000005056 compaction Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- SLBOQBILGNEPEB-UHFFFAOYSA-N 1-chloroprop-2-enylbenzene Chemical compound C=CC(Cl)C1=CC=CC=C1 SLBOQBILGNEPEB-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- MEJAPGGFIJZHEJ-UHFFFAOYSA-N 5-acetamido-1,3,4-thiadiazole-2-sulfonyl chloride Chemical compound CC(=O)NC1=NN=C(S(Cl)(=O)=O)S1 MEJAPGGFIJZHEJ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229930188104 Alkylresorcinol Natural products 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- WKYAPGVTFGNPSP-UHFFFAOYSA-N benzene;chloroethene Chemical compound ClC=C.C1=CC=CC=C1 WKYAPGVTFGNPSP-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 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
- 239000011121 hardwood Substances 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- UMIPWJGWASORKV-UHFFFAOYSA-N oct-1-yne Chemical compound CCCCCCC#C UMIPWJGWASORKV-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Description
【発明の詳細な説明】
本発明は成型フアイバーボードの製造方法に関
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of manufacturing molded fiberboard.
(従来技術)
従来の成型フアイバーボードは次のようにして
製造される。(Prior Art) A conventional molded fiberboard is manufactured as follows.
通常の湿式法で得られた比重0.6以上のフアイ
バーボードを用い、直かにあるいは該フアイバー
ボード面に水または浸透剤を添加された水を塗布
し浸透して一次フアイバーボードとし、この一次
フアイバーボードを型盤プレスにて熱圧成型し成
型フアイバーボードとする。 Using a fiberboard with a specific gravity of 0.6 or more obtained by a normal wet method, water or water to which a penetrant has been added is applied directly or permeated to the surface of the fiberboard to form a primary fiberboard. This is then hot-press molded using a mold press to form a molded fiberboard.
この場合の一次フアイバーボードは次のような
性状を有する。すなわち、繊維に水分を与えるこ
とにより柔軟性を増し成型し易くなるとともに型
盤プレス内においては繊維中のセルローズ、リグ
ニン等による接着作用によつて接着成型されるも
のである。 The primary fiberboard in this case has the following properties. That is, by adding moisture to the fibers, the fibers become more flexible and easier to mold, and in the mold press, the fibers are adhesively molded by the adhesive action of cellulose, lignin, etc. in the fibers.
しかしながらこのような一次フアイバーボード
を用いて成型フアイバーボードを製造する方法は
なお次のような問題点を残している。 However, the method of manufacturing a molded fiberboard using such a primary fiberboard still has the following problems.
比重が0.6以下であるとフアイバーボードが
脆弱となるため、型盤プレスまでのハンドリン
グが難かしくフアイバーボード自体損傷による
不良発生が多くなる。 If the specific gravity is less than 0.6, the fiberboard becomes brittle, making it difficult to handle up to the mold press and causing more defects due to damage to the fiberboard itself.
比重0.6以上であるため高温高圧でなくては
ならずまた出来た成型フアイバーボードが高比
重となる。 Since it has a specific gravity of 0.6 or more, it must be heated at high temperature and pressure, and the resulting molded fiberboard has a high specific gravity.
水分を与えるため成型を低温で長時間の熱圧
で行なわなくてはならず、(高温で熱圧を行な
うと水分の蒸発圧によるパンクが発生する)そ
のため繊維中のセルロース、リグニン等による
接着作用があまり期待できず、熱圧後スプリン
グパンクが発生し、きれいな成型ができない。
また成型フアイバーボード自体強度が低いもの
となる。 In order to add moisture, molding must be done under low temperature and long-term heat pressure (if heat pressure is performed at high temperatures, punctures will occur due to the evaporation pressure of the water). Therefore, the adhesive action of cellulose, lignin, etc. in the fibers However, spring punctures occur after hot pressing, and clean molding is not possible.
Furthermore, the strength of the molded fiberboard itself is low.
比重が高いものを成型するため、成型時繊維
の機械的破壊が発生し易く深い成型が行なえな
い。 Since fibers with high specific gravity are molded, mechanical destruction of the fibers is likely to occur during molding, making deep molding impossible.
本発明は上記のような従来の成型フアイバーボ
ードの製造方法の問題点を解決することを目的と
する。すなわち、本発明方法は、植物繊維に発泡
性物質を内蔵する熱可塑性合成樹脂カプセルを混
入した水性スラリーを構成した後、該スラリーを
抄造して植物繊維をマツト状となし、ホツトプレ
スで熱圧仮成型することにより内部繊維間に発泡
構造を形成した一次フアイバーボードを用いたも
のである。 The present invention aims to solve the problems of the conventional molded fiberboard manufacturing method as described above. That is, in the method of the present invention, an aqueous slurry is prepared by mixing plant fibers with thermoplastic synthetic resin capsules containing an expandable substance, and then the slurry is made into a mat shape, and the plant fibers are heated and compressed using a hot press. It uses a primary fiberboard that is molded to form a foamed structure between the internal fibers.
本発明は上記のような構成を有することによ
り、ハンドリングが容易で、低比重、で強度が高
く、かつ成型性能の高い成型フアイバーボードを
得ようとするものである。 The present invention aims to obtain a molded fiberboard having the above-described configuration, which is easy to handle, has a low specific gravity, has high strength, and has high molding performance.
以下本発明方法の実施例について説明する。 Examples of the method of the present invention will be described below.
(実施例の説明)
本発明は成型フアイバーボードの製造方法にお
いて、接着剤中に予め発泡剤を混合し、該発泡剤
を熱圧仮成型時に発泡し、繊維間に発泡構造を形
成せしめ、次に繊維間一部に発泡構造を保持しつ
つ成型することを骨子とするものである。(Description of Examples) The present invention is a method for manufacturing molded fiberboard, in which a foaming agent is mixed in advance into an adhesive, the foaming agent is foamed during hot-pressure pre-molding, and a foamed structure is formed between the fibers. The main idea is to mold the foam while maintaining the foamed structure in some areas between the fibers.
以下その詳細について説明する。 The details will be explained below.
植物繊維原料としては、広葉樹、針葉樹等の
木材、竹、笹、稲葉、バガス、パルプ工場より
多量に副生するノツト粕等があり、これらの原
料はチツプ化され、更に蒸煮もしくは常温浸漬
によつて軟化せしめた後、解繊して繊維化する
かくして得られた植物繊維には発泡性物質を
内蔵する熱可塑性合成樹脂カプセルおよびサイ
ズ剤、水等が添加されて水性スラリーとされ
る。 Plant fiber raw materials include hardwoods, softwoods, bamboo, bamboo, bamboo, rice leaves, bagasse, and knot lees, which are produced in large quantities from pulp mills.These raw materials are made into chips and further processed by steaming or soaking at room temperature. After softening, the plant fibers are defibrated into fibers. A thermoplastic synthetic resin capsule containing a foamable substance, a sizing agent, water, etc. are added to the thus obtained plant fibers to form an aqueous slurry.
発泡性物質を内蔵する熱可塑性合成樹脂カプセ
ルとしては次のようなものが用いられる。 The following thermoplastic synthetic resin capsules containing an expandable substance are used.
熱可塑性合成樹脂たとえばポリエチレン、ポ
リプロピレン、アクリル樹脂、メタクリル樹
脂、スチレン樹脂、塩化ビニル樹脂、塩化ビニ
リデン樹脂、アクリルニトリル樹脂、塩化ビニ
ルベンゾル樹脂などをカプセルとし、
n−ブタン、n−ペンタン、ネオペンタン、n
−ヘキサン、ネオヘキサン、シクロヘキサン、
n−オクタン、iso−オクタン等の鎖式もしく
は環式飽和炭化水素、n−ペンテン、n−ヘキ
セン、シクロヘキセン、n−オクチン等の鎖式
もしくは環式不飽和炭化水素、ベンゼン、トル
エン、キシレン等の芳香族炭化水素、エチルエ
ーテル、エチル、プロピルエーテル等のエーテ
ル類アセトン、メチルエチルケトン等のケトン
類、酢酸メチル、酢酸エチル等の酢酸エステル
類、セロンルブ、アセテート、ブチルセロソル
ブ等のアルコール類の一般に有機溶剤と呼ばれ
る有機化合物が主として含まれる加熱されるこ
とによつて揮発する揮発性物質を発泡性物質と
して内蔵する熱可塑性合成樹脂カプセルからな
る。これらの発泡性物質を内蔵する熱可塑性合
成樹脂カプセルは加熱により熱可塑性合成樹脂
カプセルが軟化されるとともに内蔵される揮発
性物質の揮発に伴なう体積膨張により発泡す
る。 Thermoplastic synthetic resins such as polyethylene, polypropylene, acrylic resins, methacrylic resins, styrene resins, vinyl chloride resins, vinylidene chloride resins, acrylonitrile resins, vinyl chloride benzol resins, etc. are used as capsules, and n-butane, n-pentane, neopentane, n-
-hexane, neohexane, cyclohexane,
Chain or cyclic saturated hydrocarbons such as n-octane, iso-octane, chain or cyclic unsaturated hydrocarbons such as n-pentene, n-hexene, cyclohexene, n-octyne, benzene, toluene, xylene, etc. Aromatic hydrocarbons, ethers such as ethyl ether, ethyl, and propyl ether; ketones such as acetone and methyl ethyl ketone; acetate esters such as methyl acetate and ethyl acetate; and alcohols such as cellolube, acetate, and butyl cellosolve. Generally called organic solvents. It consists of a thermoplastic synthetic resin capsule containing a volatile substance that evaporates when heated, which mainly contains organic compounds, as a foaming substance. The thermoplastic synthetic resin capsule containing these foamable substances is softened by heating and foams due to the volume expansion caused by the volatilization of the contained volatile substance.
この発泡剤については特公昭42−26524号公報
に詳細に記載されている。 This foaming agent is described in detail in Japanese Patent Publication No. 42-26524.
炭酸アンモニウム、重炭酸ソーダ、アゾビス
イソブチロニトリル、ジアゾアミンベンゼン、
トルエンスルホニルヒドラジド、アゾジヘキサ
ハイドロベンゾニトリル、オキソビスベンゼ
ン、スルホヒドラジド(OBSH)、ジニトロペ
ンタメチレンテトラミン(DPT)、アゾジカル
ボンアミド(ADLA)、アゾジカルボン酸ジエ
チルエステルなど加熱されることによつて分解
し、ガスを発し発泡する発泡剤を内蔵する熱可
塑性合成樹脂カプセルからなるもの。 Ammonium carbonate, sodium bicarbonate, azobisisobutyronitrile, diazoaminebenzene,
Toluenesulfonylhydrazide, azodihexahydrobenzonitrile, oxobisbenzene, sulfohydrazide (OBSH), dinitropentamethylenetetramine (DPT), azodicarbonamide (ADLA), azodicarboxylic acid diethyl ester, etc. Decomposes when heated. It consists of a thermoplastic synthetic resin capsule containing a foaming agent that emits gas and foams.
これらの発泡性物質を内蔵する熱可塑性合成樹
脂カプセルは加熱によつて熱可塑性合成樹脂カプ
セルが軟化されるとともに内蔵される発泡剤が加
熱によつて分解し、ガスを発する発泡剤の発泡に
より発泡する。 These thermoplastic synthetic resin capsules containing foamable materials are softened by heating, and the built-in foaming agent is decomposed by heating, causing foaming due to the foaming of the foaming agent that emits gas. do.
上記した熱可塑性合成樹脂カプセルに内蔵さ
れる発泡性物質として加熱することによつて昇
華する昇華性物質を用いても良い。 A sublimable substance that sublimates when heated may be used as the foamable substance contained in the thermoplastic synthetic resin capsule described above.
上記のカプセル外殻を構成する熱可塑性
合成樹脂は内蔵される揮発性物質又は発泡剤に不
溶なもの、または、発泡温度、接着剤の硬化温度
等に応じて任意選択される。 The thermoplastic synthetic resin constituting the capsule shell may be selected depending on the volatile substance or foaming agent contained therein, or depending on the foaming temperature, curing temperature of the adhesive, etc.
たとえばカプセル外殻となる熱可塑性合成樹脂
としてはポリエチレン、ポリプロピレン、アクリ
ル樹脂、スチレン樹脂、塩化ビニル樹脂、メタク
リル樹脂、塩化ビニリデン樹脂、アクリルニトリ
ル樹脂、塩化ビニルベンジル樹脂等が用いられ
る。 For example, polyethylene, polypropylene, acrylic resin, styrene resin, vinyl chloride resin, methacrylic resin, vinylidene chloride resin, acrylonitrile resin, vinylbenzyl chloride resin, etc. are used as the thermoplastic synthetic resin for the capsule shell.
サイズ剤としては、カゼイン、澱粉、ロジン等
の天然樹脂、尿素樹脂、メラミン樹脂、尿素−メ
ラミン共縮合樹脂、フエノール樹脂、アルキルフ
エノール樹脂、レゾルシン樹脂、アルキルレゾル
シン樹脂(油母頁岩等から得られるシエルオイル
レゾルシンと呼ばれるアルキルレゾルシン混合物
からなる樹脂を含む)エポキシ樹脂、ウレタン樹
脂、アルキド樹脂、アクリル樹脂、酢酸ビニル樹
脂、スチレン樹脂等の各種の熱硬化性合成樹脂、
熱可塑性合成樹脂あるいはパラフイン、ワツク
ス、あるいはこれらの混合物が用いられる。 Sizing agents include natural resins such as casein, starch, and rosin, urea resins, melamine resins, urea-melamine cocondensation resins, phenolic resins, alkylphenol resins, resorcinol resins, and alkylresorcinol resins (shell oil resorcinol obtained from oil matrix shale, etc.). various thermosetting synthetic resins such as epoxy resins, urethane resins, alkyd resins, acrylic resins, vinyl acetate resins, styrene resins, etc.
A thermoplastic synthetic resin, paraffin, wax, or a mixture thereof is used.
上記組成以外、例えば炭酸カルシウム、チタン
白、ベントナイト、タルク、木粉、小麦粉、のよ
うな充填剤、酸やアルカリ硬化触媒、ε−カプロ
ラクタム、尿素、レゾルシン等の縮合調節剤、も
しくはホルマリンキヤツチヤー剤、老化防止剤、
紫外線吸収剤、防腐剤、防虫剤、防水剤、難燃
剤、撥水剤、染料、顔料等を混合してもよい。 Compositions other than those mentioned above, such as fillers such as calcium carbonate, titanium white, bentonite, talc, wood flour, wheat flour, acid or alkali curing catalysts, condensation regulators such as ε-caprolactam, urea, resorcinol, or formalin carriers. agent, anti-aging agent,
Ultraviolet absorbers, preservatives, insect repellents, waterproofing agents, flame retardants, water repellents, dyes, pigments, etc. may be mixed.
仮圧締、熱圧締によつてマツト内から排出され
る水と共に、前記発泡剤が流出するおそれがある
場合は、該カプセルの粒径を大きくし植物繊維間
に絡ませて定着するか、凝集剤の添加、前記発泡
剤のイオン化などにより該繊維に吸着せしめても
よい。 If there is a risk that the foaming agent may flow out together with the water discharged from the pine during temporary compaction or heat compaction, the particle size of the capsules should be increased and the capsules should be entangled between plant fibers and fixed, or aggregated. The foaming agent may be adsorbed onto the fibers by adding a foaming agent or by ionizing the foaming agent.
上記組成比率は通常繊維100重量部に対して発
泡性物質を内蔵する熱可塑性合成樹脂カプセルは
0.03〜60重量部、サイズ剤は0.1〜10重量部とす
る。 The above composition ratio is usually 100 parts by weight of fiber for thermoplastic synthetic resin capsules containing a foamable substance.
The amount is 0.03 to 60 parts by weight, and the sizing agent is 0.1 to 10 parts by weight.
上記混合物に水を添加して濃度0.01〜5重量
%程度のスラリーとし、金網、フエルト、不織
布等の多孔質担体からなる抄造機、フローコー
ター、スプレー等によつて流し出してマツト状
とする。 Water is added to the above mixture to form a slurry having a concentration of about 0.01 to 5% by weight, and the slurry is poured out using a paper machine, flow coater, spray, etc. made of a porous carrier such as a wire mesh, felt, or nonwoven fabric to form a mat.
製造されたマツトは必要に応じて適当な寸法に
裁断した後、冷圧もしくは熱圧し仮成型する。 The manufactured pine is cut into appropriate dimensions as required, and then subjected to cold or hot pressing to be temporarily formed.
熱圧する場合、必要に応じてデイスタンスバー
を装置し、通常ロールプレス、盤状プレスなどが
用いられ、そのプレス圧は5〜100Kg/cm2、プレ
ス時間は0.5〜60分、熱圧の表面温度は50〜250℃
とする。 When hot pressing, a distance bar is installed as necessary, and a roll press, plate press, etc. is usually used. Temperature is 50~250℃
shall be.
また冷圧する場合は、マツトは必要な期間経過
後上記熱圧条件で加熱仮成形を行う。 In the case of cold pressing, the mat is heated and preformed under the above hot pressing conditions after the required period of time has elapsed.
このようにして繊維相互の絡み合い、あるいは
サイズ剤による繊維の結合が強化されると同時に
マツト内の発泡性物質が発泡される。発泡性物質
を内蔵する熱可塑性合成樹脂カプセルは内部の発
泡性物質が分解し、発するガスまた加熱によつて
揮発する揮発性物質の揮発に伴ない熱により可塑
化された熱可塑性合成樹脂カプセルを膨張せし
め、気泡が形成される。 In this way, the intertwining of the fibers or the bonding of the fibers by the sizing agent is strengthened, and at the same time the foamable substance within the mat is foamed. A thermoplastic synthetic resin capsule containing a foamable substance is plasticized by heat as the foamable substance inside decomposes and the gas released and the volatile substance volatilizes when heated. It expands and bubbles form.
発泡性物質の発泡に伴なう体積膨張により繊維
マツト内の内部圧力が高くなり、熱盤による外部
圧力と相俟つて繊維が相互に密着し、繊維相互の
接触面積、すなわち接着面積が増大し、または繊
維相互がサイズ剤と熱可塑性樹脂により連結さ
れ、実質的に接着面積が増大され、その接着力が
向上し機械的強度内部結合力が著しく向上する。 The internal pressure inside the fiber mat increases due to the volumetric expansion associated with the foaming of the foamable material, which, together with the external pressure from the heating plate, causes the fibers to adhere to each other, increasing the contact area between the fibers, that is, the bonding area. Alternatively, the fibers are connected to each other by the sizing agent and the thermoplastic resin, and the bonding area is substantially increased, the bonding force is improved, and the mechanical strength and internal bonding force are significantly improved.
更に繊維間に合成樹脂気泡が形成され、該繊維
間の空隙が減少されるため耐水性が向上する。 Furthermore, synthetic resin bubbles are formed between the fibers, and the voids between the fibers are reduced, resulting in improved water resistance.
かくしてフアイバーボード内の繊維間に発泡性
物質を内蔵する熱可塑性合成樹脂カプセルの発泡
に伴なう発泡構造が形成された低比重の一次フア
イバーボードが得られる。 In this way, a primary fiberboard with a low specific gravity is obtained in which a foamed structure is formed due to the foaming of a thermoplastic synthetic resin capsule containing a foamable substance between the fibers in the fiberboard.
一次フアイバーボードは低比重ではあるが、そ
の接着力、機械的強度が向上されているので充分
にハンドリングが出来る。 Although the primary fiberboard has a low specific gravity, its adhesive strength and mechanical strength are improved, so it can be handled satisfactorily.
次に一次フアイバーボードを型盤プレスに挿
入し熱圧成型する。 Next, the primary fiberboard is inserted into a mold press and hot-pressed.
一次フアイバーボードはその内部の繊維間に発
泡構造が形成され、低比重であるので型盤プレス
で容易に成型できる。 Primary fiberboard has a foamed structure formed between its internal fibers and has a low specific gravity, so it can be easily molded using a mold press.
またその熱圧時、発泡構造を構成するカプセル
が熱可塑性合成樹脂であるので低温で容易に可塑
化されるとともに、その圧力によつて発泡構造の
一部を破壊され、しかも該樹脂の接着力によつて
接着力、機械的強度を低下することなく成型が行
なわれる。 In addition, during the heat-pressing process, since the capsules that make up the foam structure are made of thermoplastic synthetic resin, they are easily plasticized at low temperatures, and a portion of the foam structure is destroyed by the pressure, and the adhesive strength of the resin Molding can be carried out without reducing adhesive strength or mechanical strength.
このようにして繊維が互いに絡み合い、かつサ
イズ剤、熱可塑性合成樹脂により接着されてお
り、該繊維間一部に加熱によつて発泡する発泡性
物質が発泡した状態を保持しつつ充填された成型
フアイバーボードが容易に得られる。また繊維間
に形成された発泡構造を全て破壊するように型盤
プレスにて成型しても何ら差し支えなく、この場
合得られる成型フアイバーボードは高比重に仕上
がる。 In this way, the fibers are intertwined with each other and bonded together using a sizing agent and a thermoplastic synthetic resin, and a foaming substance that foams when heated is filled between the fibers while maintaining the foamed state. Fiberboard is easily obtained. Further, there is no problem in molding using a die press so as to completely destroy the foamed structure formed between the fibers, and the molded fiberboard obtained in this case is finished with a high specific gravity.
(本発明の作用効果)
本発明は上記のような構成を有し、その作用効
果を要約すると次の通りである。(Actions and Effects of the Present Invention) The present invention has the above configuration, and its effects are summarized as follows.
第一次フアイバーは内部繊維間に発泡剤が発泡
状態のまま保持され発泡構造が形成され、しかも
繊維の絡み合い、熱可塑性合成樹脂のもつ接着
力、発泡による樹脂被膜の繊維相互の架橋状接
着、発泡剤の発泡に伴なう内部圧力による繊維相
互の接触面積(接着面積)の増大などにより繊維
と熱可塑性合成樹脂が強固に一体化し、低比重で
しかも機械的強度が強く充分にハンンドリングで
きる。そしてこのように第一時フアイバーボード
を型盤プレスで低い成型圧で成型すれば、一部の
発泡構造は破壊されることなく保持されたままの
成型系フアイバーボードが得られる。 The primary fiber has a foamed structure in which the foaming agent is held in a foamed state between the internal fibers, and the fibers are entangled, the adhesive force of the thermoplastic synthetic resin, and the crosslinked adhesion between the fibers of the resin coating due to foaming. Due to the increase in the contact area (adhesion area) between the fibers due to the internal pressure caused by the foaming of the foaming agent, the fibers and thermoplastic synthetic resin are firmly integrated, and the product has a low specific gravity and strong mechanical strength, making it easy to handle. . By molding the first fiberboard with a mold press at a low molding pressure in this manner, a molded fiberboard in which a portion of the foamed structure is retained without being destroyed can be obtained.
かくして得られた成型フアイバーボードは発泡
構造の一部が残存するため軽量であるとともに、
一次フアイバーボードの機械的強度をそのまま受
継ぎ、強度もまた充分である。また、型盤プレス
の金型に正確に一致した成型体を得ることができ
る。もし、発泡構造の一部が破壊されないと、発
泡構造の復元力により金型に一致した形状が得ら
れない。 The molded fiberboard thus obtained is lightweight because a portion of the foam structure remains, and
It inherits the mechanical strength of the primary fiberboard and is also strong enough. Furthermore, it is possible to obtain a molded body that accurately matches the mold of the mold press. If a portion of the foamed structure is not destroyed, a shape matching the mold cannot be obtained due to the restoring force of the foamed structure.
Claims (1)
成樹脂カプセル,サイズ剤を混入した水性スラリ
ーを抄造してマツト状とした後、ホツトプレスで
熱圧仮成型して、発泡構造を有する一次フアイバ
ーボードを構成し、 該一次フアイバーボードを型盤プレスにて熱圧
して繊維間に一部の発泡構造を保持しながら成型
フアイバーボードを得る、 ことを特徴とする成型フアイバーボードの製造方
法。[Scope of Claims] 1. Thermoplastic synthetic resin capsules containing a foamable substance in vegetable fibers, an aqueous slurry mixed with a sizing agent, made into a mat shape, and then preformed under heat and pressure using a hot press to form a foamed structure. A method for producing a molded fiberboard comprising: forming a primary fiberboard having the following properties, and hot pressing the primary fiberboard in a die press to obtain a molded fiberboard while retaining a portion of the foamed structure between the fibers. Method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3079183A JPS59157400A (en) | 1983-02-28 | 1983-02-28 | Production of molded fiberoard |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3079183A JPS59157400A (en) | 1983-02-28 | 1983-02-28 | Production of molded fiberoard |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59157400A JPS59157400A (en) | 1984-09-06 |
JPH0333840B2 true JPH0333840B2 (en) | 1991-05-20 |
Family
ID=12313494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3079183A Granted JPS59157400A (en) | 1983-02-28 | 1983-02-28 | Production of molded fiberoard |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59157400A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0722465B2 (en) * | 1985-04-08 | 1995-03-15 | 井関農機株式会社 | Seedling material |
JP2010236107A (en) * | 2009-03-30 | 2010-10-21 | Daiken Corp | Method for producing inorganic board |
CN102352089B (en) * | 2011-07-01 | 2013-03-20 | 中航复合材料有限责任公司 | Vegetable fiber reinforced biomass resin lamellar material and preparation method thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5230602A (en) * | 1975-09-04 | 1977-03-08 | Kubota Ltd | Tracting device for attachment |
-
1983
- 1983-02-28 JP JP3079183A patent/JPS59157400A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5230602A (en) * | 1975-09-04 | 1977-03-08 | Kubota Ltd | Tracting device for attachment |
Also Published As
Publication number | Publication date |
---|---|
JPS59157400A (en) | 1984-09-06 |
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