JP4726401B2 - Manufacturing method of non-combustible decorative board - Google Patents
Manufacturing method of non-combustible decorative board Download PDFInfo
- Publication number
- JP4726401B2 JP4726401B2 JP2003166423A JP2003166423A JP4726401B2 JP 4726401 B2 JP4726401 B2 JP 4726401B2 JP 2003166423 A JP2003166423 A JP 2003166423A JP 2003166423 A JP2003166423 A JP 2003166423A JP 4726401 B2 JP4726401 B2 JP 4726401B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- decorative board
- paper
- formula
- combustible decorative
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 229920005989 resin Polymers 0.000 claims description 20
- 239000011347 resin Substances 0.000 claims description 20
- 239000000853 adhesive Substances 0.000 claims description 11
- 230000001070 adhesive effect Effects 0.000 claims description 11
- 229920000877 Melamine resin Polymers 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 238000000465 moulding Methods 0.000 claims description 8
- 239000004745 nonwoven fabric Substances 0.000 claims description 8
- 239000002002 slurry Substances 0.000 claims description 8
- 239000011256 inorganic filler Substances 0.000 claims description 7
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 7
- 239000012792 core layer Substances 0.000 claims description 6
- 230000005484 gravity Effects 0.000 claims description 6
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 5
- 239000003365 glass fiber Substances 0.000 claims description 5
- 239000005011 phenolic resin Substances 0.000 claims description 5
- 239000002344 surface layer Substances 0.000 claims description 3
- 239000012784 inorganic fiber Substances 0.000 description 11
- 239000003822 epoxy resin Substances 0.000 description 9
- 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 9
- 229920000647 polyepoxide Polymers 0.000 description 9
- 239000002585 base Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- ZHNUHDYFZUAESO-OUBTZVSYSA-N aminoformaldehyde Chemical compound N[13CH]=O ZHNUHDYFZUAESO-OUBTZVSYSA-N 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 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
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- -1 octylphenol Chemical compound 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Description
【0001】
【産業上の利用分野】
本発明は、不燃化粧板の製造方法に関する。
【0002】
【特許文献1】
特開昭64−56540号公報
【特許文献2】
特開平03−208632号公報
【特許文献3】
特開2000−104366号公報
【特許文献4】
特開昭53−94578号公報
【0003】
【従来の技術】
従来、防火、不燃性を付与した化粧板が知られており、コア層には無機繊維不織布に有機樹脂をバインダー成分とスラリーが含浸されたプリプレグが用いられ、化粧層と必要に応じて表面層とを積層し、温度120〜140℃、圧力60〜70kg/cm2の条件で熱圧成形され、化粧層には樹脂含浸化粧紙が用いられていた。
【0004】
【発明が解決しようとする課題】
しかしながら、高圧成形するため無機繊維不織布の下地の影響で化粧表面が綺麗に仕上がらない、プリプレグの積層枚数を増やして厚みを大きくしようとしても有機樹脂分が多くなり不燃性の確保ができない、比重が高くなり製品重量が重くなるなどの問題があった。
【0005】
【課題を解決するための手段】
本発明は、かかる状況に鑑み検討されたもので、不燃性能を有し、かつ反りの少ない化粧板を得ることを目的とするもので、以下のことを特徴とする。
【0006】
すなわち、請求項1の記載の発明は、ガラス繊維不織布に、有機樹脂分としてのフェノール樹脂とメラミン−ホルムアルデヒド樹脂と、無機充填材としての水酸化アルミニウムとからなるスラリーを式1で示される含有率(%)が3〜50%となるように含浸したプリプレグからなるコア層と、表面層としてコート紙を接着材を介して積層し、熱圧成形後の比重が1.4〜1.8となるように、圧力15〜40kg/cm 2 の条件で熱圧成形することを特徴とする不燃化粧板の製造方法である。
また、請求項2に記載の発明は、裏面側にバランス紙を配することを特徴とする請求項1記載の不燃化粧板の製造方法である。
以下、本発明について詳細に説明する。
【0007】
本発明の不燃化粧板のコア層に用いる無機繊維基材としては、ガラス繊維、ロックウール、炭素繊維などの無機繊維の不織布、織布などが挙げられ、無機繊維基材の坪量は、10〜200g/m2の範囲が好適であり、とりわけ、耐熱性、耐炎性に優れ、スラリーの含浸性が優れるガラス繊維を用いるのが好ましい。
【0008】
バインダーとしての有機樹脂成分は、具体的にフェノール樹脂、アミノ−ホルムアルデヒド樹脂、ウレタン樹脂、エポキシ樹脂などが挙げられ、二種以上を併用してもよい。
【0009】
フェノール樹脂は、フェノール類とアルデヒド類とをフェノール性水酸基1モルに対してアルデヒド類を1〜3モルの割合で塩基性触媒下或いは酸性触媒下にて反応させて得られるもので、フェノール類としては、フェノール、クレゾール、キシレノール、オクチルフェノール、フェニルフェノール、ビスフェノールA、ビスフェノールS、ビスフェノールFなどが挙げられ、アルデヒド類としては、ホルムアルデヒド、パラホルムアルデヒド、グリオキザール、トリオキザールなどが挙げられる。
また、必要に応じてパラトルエンスルフォンアミド、桐油、燐酸エステル類、グリコール類などの可塑化を促す変性剤で変性されたものも適用でき、塩基性触媒としては、ナトリウム、カリウムなどのアルカリ金属、及びマグネシウム、カルシウムなどのアルカリ土類金属の酸化物や水酸化物、及びトリエチルアミン、トリエタノールアミンなどのアミン類、アンモニアが挙げられ、酸性触媒としては、パラトルエンスルフォン酸、塩酸などが挙げられる。
【0010】
アミノ−ホルムアルデヒド樹脂としてはアミノ化合物、例えばメラミン、尿素、ベンゾグアナミン、アセトグアナミンなどとホルムアルデヒドを反応させた初期縮合物のほか、メチルアルコール、ブチルアルコールなどの低級アルコ−ルによるエ−テル化、パラトルエンスルホンアミドなどの可塑化を促す反応性変性剤で変性されたものが適用でき、中でも耐久性に優れるメラミン−ホルムアルデヒド樹脂が好ましい。
【0011】
ウレタン樹脂は、トリレンジイソシアネート、ジフェニルメタンジイソシアネート、キシリレンジイソシアネート、ヘキサメチレンジイソシアネート、イソホロンジイソシアネート等のイソシアネート基を有する化合物を原料とするプレポリマー、アダクト体、ブロックイソシアネートなどが挙げられる。
【0012】
エポキシ樹脂としては、少なくとも一分子中に2個以上のエポキシ基を有するビスフェノールA型エポキシ樹脂、一分子中に2個以上のエポキシ基を有するフェノールノボラック型エポキシ樹脂、オルソクレゾールノボラック型エポキシ樹脂、ビスフェノールF型エポキシ樹脂、脂環式エポキシ樹脂、3官能以上の多官能エポキシ樹脂及びこれらの臭素化物、さらにこれらの混合物が挙げられ、積層板に用いられる通常のエポキシ樹脂を使用することができる。
【0013】
無機充填剤としては、水酸化アルミニウム、水酸化マグネシウム、炭酸カルシウム、シリカなどが挙げられる。無機繊維不織布の坪量は、10〜200g/m2の範囲が好適である。
無機充填剤の中では、平均粒子径が0.5〜200μmの範囲のものが無機性繊維不織布への含浸が可能であり、水酸化アルミニウムや水酸化マグネシウムなど結晶水を含むものは高温時に分解し、吸熱、結合水を放出するため不燃性の効果の点で最適である。
【0014】
プリプレグ中の有機樹脂成分の含有率は、式1で示される算出方法で3〜50%であればよく、上限を越えると不燃性が悪くなり、下限を超えると強度、密着性が劣りやすくなる。
【式1】
【0015】
無機繊維を基材とするプリプレグとは、無機繊維基材に有機樹脂成分と無機充填剤からなるスラリーを含浸したもので、無機繊維基材、有機樹脂成分、無機充填剤いずれも前述と同様のものを用いることができ、必ずしも同種のものを用いる必要はない。
プリプレグ中のスラリー含有率(%)は式2で示される算出方法で、500〜3000%の範囲が好ましく、上限を超えると固形分の脱落が多くなり取り扱いにくく、また下限に満たないと層間剥離しやすくなる。
【式2】
【0016】
プリプレグからなるコア層の少なくとも片面には、後述のコート紙との密着性を向上させるため接着材が介される。
接着材としては、18〜40g/m2の化粧板用表面紙に熱硬化性樹脂、例えば、アミノ−ホルムアルデヒド樹脂、ジアリルフタレート樹脂、不飽和ポリエステル樹脂、或いはこれらの混合物などを主な成分とする樹脂液が式3で示される含浸率が80〜300%含浸・乾燥された樹脂含浸シートや、酢酸ビニル樹脂系接着剤の如き合成樹脂接着剤を紙に塗布したものなどが挙げられる。
【式3】
【0017】
接着材の上には化粧層としてコート紙が積層される。コート紙は、40〜80g/m2の化粧紙の表面にウレタン樹脂、アミノアルキッド樹脂、アクリレート樹脂などの合成樹脂を塗布したもので、コア層と、接着材とを積層一体化するには平板プレス、連続プレスなどのプレス機を用いて熱圧成形すればよいが、比重が1.4〜1.8となるように、圧力は通常の化粧板を得る場合よりも低圧、具体的には15〜40kg/cm2の範囲で成形する。比重が下限に満たないと、強度不足を生じたり密着性が劣りやすくなる。また、上限を超えると不燃性が劣りやすくなる。
【0018】
尚、硬化収縮に伴う反りを抑制するため最下層にバランス紙を配することが望ましく、バランス紙としては同様の樹脂含浸シートや、紙に酢酸ビニル樹脂系接着剤の如き合成樹脂接着剤を塗布したものが挙げられる。
【0019】
【実施例】
以下、実施例、比較例を挙げてより詳細に説明するが、本発明をより具体的に示すものであって、特に限定するものではない。
実施例1
プリプレグ
50g/m2のガラス繊維不織布に、フェノール樹脂5部に対して、メラミン−ホルムアルデヒド樹脂4部、水酸化アルミニウムを91部配合したスラリーを、式2に示す固形分率が2000%となるように含浸してプリプレグを得た。
接着シート
坪量22g/m2の表面紙に,メラミン−ホルムアルデヒド樹脂を式3で示す含浸率が250%となるように含浸してメラミン樹脂含浸シートを得た。
不燃化粧板
下から順に、メラミン樹脂含浸シートを1枚、プリプレグを4枚、メラミン樹脂含浸シートを1枚、65g/m2の印刷紙に変性アクリレート樹脂15g/m2塗布したコート紙を1枚積層して、フラット仕上げプレートを用いて140℃、35kg/cm2、60分間で熱圧成形して、実施例1の不燃化粧板を得た。
【0020】
実施例2
下から順に、35g/m2の紙に酢酸ビニル樹脂を塗布したシートを1枚、実施例1と同様のプリプレグを4枚積層し、酢酸ビニル樹脂接着剤を介して実施例1と同様のコート紙を1枚積層して、フラット仕上げプレートを用いて140℃、35kg/cm2、60分間で熱圧成形して、実施例2の不燃化粧板を得た。
【0021】
比較例1(成形圧力が下限未満の場合)
実施例1において、成形圧力を10kg/cm2とした以外は同様に実施して、比較例1の化粧板を得た。
【0022】
比較例2(成形圧力が上限を超える場合)
実施例1において、成形圧力を70kg/cm2とした以外は同様に実施して、比較例1の化粧板を得た。
【0023】
評価結果を表1に示す。
【表1】
【0024】
試験方法は以下の通りとした。
不燃性:建築基準法第2条第9号規定「4.9.2 発熱性試験・評価方法」による。(ISO5660準拠したコーンカロリーメーターによる20分試験)強度:500gの鉄球をサンプルの20cm上方より落下させ、割れなかったものを○、割れたものを×とした。
密着性:化粧層にカッターナイフにてクロスカットの切り込みをコア層に達する深さまで入れ、セロハンテープを貼り付け、急激に剥がし、化粧層の剥離がなかったものを○、剥離があったものを×とした。
【0025】
【発明の効果】
本発明は、無機繊維基材に有機樹脂成分と無機充填剤からなるスラリーを含浸し乾燥したプリプレグと、コート紙とを樹脂含浸表面紙を介して、圧力が15〜40kg/cm2と通常より低圧成形し、積層一体化して、比重を1.4〜1.8とすることにより、目的成形品厚みを持ち、軽量且つ十分な強度を持ち、不燃性を持つ不燃化粧材を得ることが出来た。
【図面の簡単な説明】
【図1】 実施例1の不燃化粧板の構成断面図。
【符号の説明】
2 プリプレグ
3 樹脂含浸シート
4 コート紙
6 不燃化粧板[0001]
[Industrial application fields]
The present invention relates to a method for manufacturing a non-combustible decorative board.
[0002]
[Patent Document 1]
Japanese Patent Application Laid-Open No. 64-56540 [Patent Document 2]
Japanese Patent Laid-Open No. 03-208632 [Patent Document 3]
JP 2000-104366 A [Patent Document 4]
Japanese Patent Laid-Open No. 53-94578
[Prior art]
Conventionally, a decorative board imparted with fireproofing and nonflammability is known, and a prepreg in which an inorganic fiber nonwoven fabric is impregnated with a binder component and a slurry is used for a core layer, and a decorative layer and a surface layer as necessary And was hot-press molded under conditions of a temperature of 120 to 140 ° C. and a pressure of 60 to 70 kg / cm 2 , and resin-impregnated decorative paper was used for the decorative layer.
[0004]
[Problems to be solved by the invention]
However, because of high-pressure molding, the decorative surface is not finished cleanly due to the influence of the inorganic fiber nonwoven fabric base, and even if you try to increase the thickness by increasing the number of prepregs laminated, the organic resin content increases and it is impossible to ensure nonflammability, the specific gravity There were problems such as high product weight.
[0005]
[Means for Solving the Problems]
The present invention has been studied in view of such a situation, and an object of the present invention is to obtain a decorative board having nonflammability and less warping, and is characterized by the following.
[0006]
That is, the invention described in claim 1 is a glass fiber nonwoven fabric in which a slurry comprising a phenol resin as an organic resin component, a melamine-formaldehyde resin, and aluminum hydroxide as an inorganic filler is represented by the formula 1. (%) is a core layer made of impregnated prepreg so that 3-50%, the coated paper was laminated with an adhesive material as the surface layer, the specific gravity after the heat molding is 1.4 to 1.8 Thus, the present invention provides a method for producing a non-combustible decorative board , which is hot- press molded under a pressure of 15 to 40 kg / cm 2 .
The invention described in claim 2 is the method for manufacturing a non-combustible decorative board according to claim 1, characterized in that a balance paper is arranged on the back side.
Hereinafter, the present invention will be described in detail.
[0007]
Examples of the inorganic fiber base material used for the core layer of the incombustible decorative board of the present invention include non-woven fabrics and woven fabrics of inorganic fibers such as glass fiber, rock wool, and carbon fiber. The basis weight of the inorganic fiber base material is 10 The range of ˜200 g / m 2 is preferable, and it is particularly preferable to use glass fibers that are excellent in heat resistance and flame resistance and excellent in impregnation of slurry.
[0008]
Specific examples of the organic resin component as the binder include phenol resins, amino-formaldehyde resins, urethane resins, and epoxy resins, and two or more of them may be used in combination.
[0009]
Phenol resins are obtained by reacting phenols and aldehydes at a ratio of 1 to 3 moles of aldehydes with 1 mole of phenolic hydroxyl group under a basic catalyst or an acidic catalyst. Phenol, cresol, xylenol, octylphenol, phenylphenol, bisphenol A, bisphenol S, bisphenol F, and the like. Examples of aldehydes include formaldehyde, paraformaldehyde, glyoxal, and trioxal.
In addition, those modified with a modifying agent that promotes plasticization such as paratoluene sulfonamide, tung oil, phosphoric esters, glycols, etc. can be applied as necessary, and basic catalysts include alkali metals such as sodium and potassium, And oxides and hydroxides of alkaline earth metals such as magnesium and calcium, amines such as triethylamine and triethanolamine, and ammonia. Examples of acidic catalysts include paratoluenesulfonic acid and hydrochloric acid.
[0010]
Amino-formaldehyde resins include initial condensates obtained by reacting amino compounds such as melamine, urea, benzoguanamine and acetoguanamine with formaldehyde, etherification with lower alcohols such as methyl alcohol and butyl alcohol, and paratoluene. Those modified with a reactive modifier that promotes plasticization such as sulfonamide can be applied, and among them, a melamine-formaldehyde resin excellent in durability is preferable.
[0011]
Examples of the urethane resin include prepolymers, adducts, block isocyanates, and the like made from compounds having an isocyanate group such as tolylene diisocyanate, diphenylmethane diisocyanate, xylylene diisocyanate, hexamethylene diisocyanate, and isophorone diisocyanate.
[0012]
Epoxy resins include bisphenol A type epoxy resins having at least two epoxy groups in one molecule, phenol novolac type epoxy resins having two or more epoxy groups in one molecule, orthocresol novolac type epoxy resins, bisphenols. Examples thereof include F-type epoxy resins, alicyclic epoxy resins, trifunctional or higher polyfunctional epoxy resins and brominated products thereof, and mixtures thereof, and ordinary epoxy resins used for laminates can be used.
[0013]
Examples of the inorganic filler include aluminum hydroxide, magnesium hydroxide, calcium carbonate, silica and the like. The basis weight of the inorganic fiber nonwoven fabric is preferably in the range of 10 to 200 g / m2.
Among inorganic fillers, those with an average particle size in the range of 0.5 to 200 μm can be impregnated into inorganic fiber nonwoven fabrics, and those containing crystal water such as aluminum hydroxide and magnesium hydroxide decompose at high temperatures. It is optimal in terms of nonflammability because it absorbs heat and binds water.
[0014]
The content of the organic resin component in the prepreg may be 3 to 50% according to the calculation method shown in Formula 1. If the upper limit is exceeded, the nonflammability becomes worse, and if the lower limit is exceeded, the strength and adhesion tend to be poor. .
[Formula 1]
[0015]
A prepreg based on an inorganic fiber is obtained by impregnating an inorganic fiber base material with a slurry comprising an organic resin component and an inorganic filler, and the inorganic fiber base material, the organic resin component, and the inorganic filler are the same as described above. It is not necessary to use the same type.
The slurry content (%) in the prepreg is calculated by the formula 2 and is preferably in the range of 500 to 3000%. If the upper limit is exceeded, the solid content will drop off and it will be difficult to handle. It becomes easy to do.
[Formula 2]
[0016]
An adhesive is interposed on at least one side of the core layer made of the prepreg in order to improve the adhesion to the coated paper described later.
The main component of the adhesive is 18-40 g / m 2 of decorative paper surface paper and a thermosetting resin such as amino-formaldehyde resin, diallyl phthalate resin, unsaturated polyester resin, or a mixture thereof. Examples thereof include a resin-impregnated sheet obtained by impregnating and drying an impregnation rate of 80 to 300% represented by the formula 3 and a resin resin coated with a synthetic resin adhesive such as a vinyl acetate resin adhesive.
[Formula 3]
[0017]
On the adhesive coated paper is laminated as a facing layer. Coated paper is made by applying synthetic resin such as urethane resin, amino alkyd resin, acrylate resin, etc. to the surface of 40-80 g / m 2 decorative paper. It may be hot-pressed using a press such as a press or a continuous press, but the pressure is lower than that for obtaining a normal decorative board so that the specific gravity is 1.4 to 1.8, specifically, molded in a range of 15~40 k g / cm 2. If the specific gravity is less than the lower limit, insufficient strength or adhesiveness tends to be inferior. Moreover, when it exceeds an upper limit, nonflammability will become inferior easily.
[0018]
In addition, it is desirable to place a balance paper on the bottom layer to suppress warping due to curing shrinkage. As the balance paper, a similar resin-impregnated sheet or a synthetic resin adhesive such as vinyl acetate resin adhesive is applied to the paper. The thing which was done is mentioned.
[0019]
【Example】
Hereinafter, although an Example and a comparative example are given and demonstrated in detail, this invention is shown more concretely and is not specifically limited.
Example 1
A slurry in which 4 parts of melamine-formaldehyde resin and 91 parts of aluminum hydroxide are blended with 5 parts of phenol resin in a glass fiber nonwoven fabric of prepreg 50 g / m 2 so that the solid content ratio shown in Formula 2 is 2000%. To obtain a prepreg.
A melamine resin-impregnated sheet was obtained by impregnating a surface paper having an adhesive sheet basis weight of 22 g / m 2 with a melamine-formaldehyde resin so that the impregnation ratio represented by Formula 3 was 250%.
In order from the bottom of the non-combustible decorative board, 1 sheet of melamine resin impregnated sheet, 4 sheets of prepreg, 1 sheet of melamine resin impregnated sheet, 1 sheet of coated paper coated with 15 g / m 2 of modified acrylate resin on 65 g / m 2 printing paper It laminated | stacked and it hot-press-molded at 140 degreeC and 35 kg / cm < 2 > for 60 minutes using the flat finish plate, and obtained the nonflammable decorative board of Example 1. FIG.
[0020]
Example 2
In order from the bottom, one sheet of 35 g / m 2 paper coated with vinyl acetate resin and four prepregs similar to those in Example 1 are laminated, and the same coating as in Example 1 is applied via a vinyl acetate resin adhesive. One sheet of paper was laminated and hot-press molded at 140 ° C. and 35 kg / cm 2 for 60 minutes using a flat finish plate to obtain a non-combustible decorative board of Example 2.
[0021]
Comparative Example 1 (when the molding pressure is less than the lower limit)
In Example 1, except that the molding pressure was 10 k g / cm 2 is carried out analogously to obtain the decorative board of Comparative Example 1.
[0022]
Comparative Example 2 (when the molding pressure exceeds the upper limit)
In Example 1, except that the molding pressure was 70 k g / cm 2 is carried out analogously to obtain the decorative board of Comparative Example 1.
[0023]
The evaluation results are shown in Table 1.
[Table 1]
[0024]
The test method was as follows.
Nonflammability: According to Article 4, Item 9 of the Building Standards Law, “4.9.2 Exothermic test and evaluation method”. (20-minute test with a cone calorimeter based on ISO 5660) Strength: A 500 g iron ball was dropped from above 20 cm of the sample.
Adhesiveness: Insert a crosscut into the decorative layer with a cutter knife to a depth that reaches the core layer, affix the cellophane tape, and peel off rapidly. X.
[0025]
【The invention's effect】
In the present invention, the inorganic fiber base material is impregnated with a slurry composed of an organic resin component and an inorganic filler and dried, and the coated paper is coated with a resin-impregnated surface paper, and the pressure is 15 to 40 kg / cm 2. Low-pressure molding, layered integration, and specific gravity of 1.4-1.8 can provide a non-combustible cosmetic material with the desired molded product thickness, light weight, sufficient strength, and non-flammability. It was.
[Brief description of the drawings]
FIG. 1 is a cross-sectional view illustrating a configuration of a non-combustible decorative board according to a first embodiment.
[Explanation of symbols]
2 Prepreg 3 Resin impregnated sheet 4 Coated paper 6 Non-combustible decorative board
Claims (2)
【式1】
A glass fiber non-woven fabric is made of a slurry composed of a phenol resin as an organic resin , a melamine-formaldehyde resin, and aluminum hydroxide as an inorganic filler so that the content (%) represented by Formula 1 is 3 to 50%. a core layer made of impregnated prepreg, the coated paper was laminated with an adhesive material as the surface layer, as the specific gravity after the heat molding is 1.4 to 1.8, the pressure 15~40kg / cm A method for producing a non-combustible decorative board , which is hot-press molded under the condition of 2 .
[Formula 1]
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| Application Number | Priority Date | Filing Date | Title |
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| JP2003166423A JP4726401B2 (en) | 2003-06-11 | 2003-06-11 | Manufacturing method of non-combustible decorative board |
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| Application Number | Priority Date | Filing Date | Title |
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| JP2003166423A JP4726401B2 (en) | 2003-06-11 | 2003-06-11 | Manufacturing method of non-combustible decorative board |
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| JP4726401B2 true JP4726401B2 (en) | 2011-07-20 |
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| JP4771776B2 (en) * | 2005-09-21 | 2011-09-14 | アイカ工業株式会社 | Flexible decorative board |
| CN117754929A (en) * | 2023-11-07 | 2024-03-26 | 浙江瑞欣装饰材料有限公司 | An environmentally friendly non-combustible decorative board |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS6456540A (en) * | 1987-08-28 | 1989-03-03 | Aica Kogyo Co Ltd | Nonflammable decorative material |
| JPH0252739A (en) * | 1988-08-18 | 1990-02-22 | Dainippon Printing Co Ltd | Manufacture of decorative sheet having smooth surface |
| JPH06143484A (en) * | 1992-01-10 | 1994-05-24 | Aica Kogyo Co Ltd | Non-flammable decorative board |
| JP3463923B2 (en) * | 1999-08-10 | 2003-11-05 | 旭ファイバーグラス株式会社 | Method for producing cosmetic inorganic moldings |
| JP2002210882A (en) * | 2001-01-18 | 2002-07-31 | Aica Kogyo Co Ltd | Non-combustible molded sheet |
| JP3875846B2 (en) * | 2001-02-22 | 2007-01-31 | タキロン株式会社 | Incombustible decorative board |
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