JPH10114021A - Laminated finishing material - Google Patents
Laminated finishing materialInfo
- Publication number
- JPH10114021A JPH10114021A JP24189797A JP24189797A JPH10114021A JP H10114021 A JPH10114021 A JP H10114021A JP 24189797 A JP24189797 A JP 24189797A JP 24189797 A JP24189797 A JP 24189797A JP H10114021 A JPH10114021 A JP H10114021A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- sheet
- sheet material
- decorative
- base material
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 100
- 239000011347 resin Substances 0.000 claims abstract description 29
- 229920005989 resin Polymers 0.000 claims abstract description 29
- 239000003365 glass fiber Substances 0.000 claims abstract description 13
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 12
- 239000005011 phenolic resin Substances 0.000 claims description 8
- 239000002023 wood Substances 0.000 claims description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 229920003002 synthetic resin Polymers 0.000 claims description 2
- 239000000057 synthetic resin Substances 0.000 claims description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 2
- 239000007779 soft material Substances 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 description 18
- 239000004745 nonwoven fabric Substances 0.000 description 9
- 239000000123 paper Substances 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 239000011120 plywood Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 238000007731 hot pressing Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000003014 reinforcing effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 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 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 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
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011521 glass 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
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002990 reinforced plastic Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- -1 veneer Substances 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
Landscapes
- Panels For Use In Building Construction (AREA)
- Laminated Bodies (AREA)
- Finished Plywoods (AREA)
- Finishing Walls (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】この発明は、建築用内装材と
して床,壁,天井等に用いられ、あるいは家具や自動車
の内装材、さらには各種造作の表面仕上材等として使用
される積層仕上材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a laminated finishing material used as a building interior material for floors, walls, ceilings, etc., or as a furniture or automobile interior material, or as a surface finishing material for various works. About.
【0002】[0002]
【従来の技術】内装の仕上材に関しては、合板等の表面
に薄い化粧板を貼った積層仕上材が広く用いられてい
る。あるいは、パーティクルボードや合板の表面に塩化
ビニルシート、印刷された紙やプラスチックシート等を
貼ったりしたものが知られている。2. Description of the Related Art As an interior finishing material, a laminated finishing material in which a thin decorative board is stuck on the surface of a plywood or the like is widely used. Alternatively, a material in which a vinyl chloride sheet, printed paper, a plastic sheet, or the like is attached to the surface of a particle board or a plywood is known.
【0003】[0003]
【発明が解決しようとする課題】内装仕上材に関して
は、用途上物に接触することが多く、その為、仕上げ表
面に傷(特にヘコミ)がつき、外観が悪くなる欠点があ
った。特に化粧材が突き板,紙等のような薄ものの場
合、ヘコミによる表面の破れ等が防止できなかった。However, the interior finishing material often comes into contact with an object for the purpose of use, so that the finished surface is scratched (especially dents) and the appearance is deteriorated. In particular, when the decorative material is a thin material such as veneer, paper, or the like, it is impossible to prevent the surface from being broken due to dents.
【0004】そこで、この発明は、化粧材の直下の層に
硬質な層を形成することにより、化粧材が薄板あるいは
軟質材であっても、仕上材として傷のつきにくい材料に
することができるようにした、すなわち耐傷性に優れた
積層仕上材を安価に提供することを目的とする。Therefore, according to the present invention, by forming a hard layer directly below the decorative material, even if the decorative material is a thin plate or a soft material, it can be made a material which is hardly damaged as a finishing material. In other words, an object of the present invention is to provide a laminated finishing material having excellent scratch resistance at low cost.
【0005】[0005]
【課題を解決するための手段】上述の目的を達成するた
め、この発明は、基材上にガラス繊維を含むシート材を
重ね合わせ、基材とシート材の両者の全体又は一部に熱
硬化性樹脂を含浸させて互いに接着し、シート材上に化
粧材を貼着したものである。SUMMARY OF THE INVENTION In order to achieve the above-mentioned object, the present invention relates to a method of laminating a sheet material containing glass fibers on a base material, and thermally curing the whole or a part of both the base material and the sheet material. It is impregnated with a conductive resin and adhered to each other, and a decorative material is stuck on a sheet material.
【0006】[0006]
【発明の実施の形態】以下に、この発明の好適な実施例
を図面を参照にして説明する。Preferred embodiments of the present invention will be described below with reference to the accompanying drawings.
【0007】図1に示す実施例は、基材1上にガラス繊
維を含むシート材2を重ね合わせ、基材1とシート材2
の両者の全体又は一部に熱硬化性樹脂3を含浸させて互
いに接着し(基材1とシート材2とが接着されたものを
符号10で示す)、この部材10のシート材2上に化粧
材4を貼着したものを示す。In the embodiment shown in FIG. 1, a sheet material 2 containing glass fibers is superimposed on a base material 1, and the base material 1 and the sheet material 2
Are impregnated with the thermosetting resin 3 on the whole or a part thereof and adhered to each other (the base material 1 and the sheet material 2 are adhered to each other by reference numeral 10). Shown is a decorative material 4 attached.
【0008】基材1としては、熱硬化性樹脂の含浸を可
能とする材質、例えば合板,木質系繊維ボード,パーテ
ィクルボード,ウェハーボード等あるいはこれらの複合
板が好適に使用できる。As the base material 1, a material that can be impregnated with a thermosetting resin, for example, a plywood, a wood fiber board, a particle board, a wafer board, or a composite board thereof can be suitably used.
【0009】シート材2としては、ガラス繊維を含む織
布,不織布が好適に使用できる。織布としては、例えば
1200デニールのガラス繊維を縦方向に3本/cm、横
方向に3本/cmとしたものが使用でき、ガラス繊維を含
む不織布としては、含浸性,脱泡性,シート基材強度,
ハンドリング,成形品の耐傷性の点から、坪量が10〜
1000g/m2 、より好ましくは50〜250g/m
2 で、繊維長の短い短繊維(3mm以上)と10mm以上の
長繊維(50mm以下)の混合されたものが好適である。
ガラス不織布は、坪量が10g/m2 より少ないと、耐
傷性が発現しにくく、1000g/m2 より多いと、樹
脂の含浸が困難となる。ガラス繊維の長さも3mm未満の
短繊維では、補強効果が低く、一方50mmを越える長繊
維では、均一シート化が困難であり、結果として優れた
補強効果が得られない。また、3〜15mmの短繊維が全
繊維中20〜100%であることが、強度(補強性)、
不織布の均一性の観点からは好ましい。短繊維が20%
より少ないと不織布の均一性が図れない。これら繊維材
料の他に短繊維のセルロースパルプ等を混合することは
差し支えない。また、ガラス繊維を用いる場合は、繊維
表面をシランカップリング剤でコートしておくことによ
り、補強効果を高めることができる。ガラス繊維を含む
不織布は、原料繊維を接着もしくは絡み合わせ或いはそ
の双方を用いて機械的,化学的,加熱的もしくは溶媒を
用いる方法、或いはそれらの組合せによってシート状に
形成される。繊維原料を湿式抄紙もしくは乾式不織布製
造法によりマット化したものをバインダー樹脂で結合し
たものが好適に使用できる。As the sheet material 2, a woven or non-woven fabric containing glass fibers can be suitably used. As the woven cloth, for example, a glass fiber of 1200 denier having a length of 3 fibers / cm in the longitudinal direction and a width of 3 fibers / cm in the horizontal direction can be used. Substrate strength,
From the viewpoint of handling and the scratch resistance of the molded product, the basis weight is 10
1000 g / m 2 , more preferably 50 to 250 g / m
2 , a mixture of short fibers having a short fiber length (3 mm or more) and long fibers having a length of 10 mm or more (50 mm or less) is preferable.
If the basis weight of the glass nonwoven fabric is less than 10 g / m 2 , it is difficult to develop scratch resistance, and if the basis weight is more than 1000 g / m 2 , it becomes difficult to impregnate the resin. Short fibers having a glass fiber length of less than 3 mm have a low reinforcing effect, while long fibers exceeding 50 mm make it difficult to form a uniform sheet, and as a result, an excellent reinforcing effect cannot be obtained. In addition, that the short fiber of 3 to 15 mm accounts for 20 to 100% of the total fiber, the strength (reinforcement),
It is preferable from the viewpoint of the uniformity of the nonwoven fabric. 20% short fibers
If the amount is less, uniformity of the nonwoven fabric cannot be achieved. Mixing short fiber cellulose pulp or the like in addition to these fiber materials may be used. When using glass fibers, the reinforcing effect can be enhanced by coating the fiber surface with a silane coupling agent. The non-woven fabric containing glass fibers is formed into a sheet by a method of mechanically, chemically, thermally or using a solvent by bonding and / or entanglement of raw fibers, or a combination thereof. A material obtained by matting fiber raw materials by a wet papermaking or dry nonwoven fabric manufacturing method and bonding them with a binder resin can be suitably used.
【0010】熱可塑性樹脂3のシート材2と基材1への
含浸は、シート材2に予め半硬化状態で含浸させてお
き、この半硬化状態の樹脂が含浸されたシート材2(プ
リプレグ)を基材1に重ね合わせて熱プレスすることで
実現できる。シート材2に含浸させる樹脂は、例えば、
フェノール類とアルデヒド類との反応により得られるフ
ェノール樹脂,末端に反応性のエポキシ基を持つオリゴ
マーに硬化剤を添加して得られるエポキシ樹脂,ユリア
樹脂,ウレタン樹脂が好適に使用できる。これらの樹脂
は単独もしくは複数混合されて主として含浸により繊維
材料(シート材2)と複合化する。シート材2に含浸す
る樹脂溶液として、水溶液,溶剤ワニス,エマルジョン
等いずれでもよく、固形樹脂粉末を散布するやり方でも
よい。この中でもコスト、安全性の点から水,アルコー
ル等に溶解もしくは分散させたものを用いることが好ま
しい。さらにこれらに各種の充填剤、例えばステアリン
酸鉛,ジブチル錫ジラウレート,カーボンブラック,炭
酸カルシウム,チタンホワイト,雲母,ガラス球,水酸
化アルミニウム,酸化アンチモン,トリ(2,3ジプロ
モプロピル)ホスフェート,脂肪族スルフォン酸塩,高
級アルコール酸塩エステル等、熱安定剤,強化剤,難燃
剤,帯電防止剤等が配合されて使用される。また、フェ
ノール樹脂の製造に必要な触媒としては、アルキルアミ
ン,アンモニア,水酸化ナトリウム,水酸化バリウム等
が好ましい。特に、アルキルアミン,アンモニアについ
ては他の2つに比べ分子量も大きく、分子構造上、水和
性が低いので貼り合わせ後の耐水性が飛躍的に向上す
る。この時、フェノール樹脂は、固形分20〜75%と
なるように水又はアルコールに溶解もしくは分散されて
いることが含浸の容易さの点から好ましい。アルコール
を用いる場合、沸点が低く乾燥しやすいので、MeOH
が好適である。固形分が20%未満だと必要量含浸する
ことが困難となり、75%より多いと粘度上昇により含
浸が困難となる。また、シート材2へ含浸させる樹脂
は、対繊維比率(重量比)50%以上含有し、望ましく
は100〜300%である。またシート材2への含浸時
において、固形分50〜500g/m2 、好ましくは1
50〜350g/m2 になるようにすることが好まし
い。50g/m2 未満だと充分な耐傷性を発現しにく
く、500g/m2 以下でなければ硬化時間がかかり、
端部からのはみだし等外観上も問題がある。The sheet material 2 and the base material 1 are impregnated with the thermoplastic resin 3 in a semi-cured state beforehand, and the sheet material 2 (prepreg) impregnated with the semi-cured resin is used. Can be realized by superimposing on the base material 1 and hot pressing. The resin to be impregnated in the sheet material 2 is, for example,
Phenol resins obtained by the reaction of phenols and aldehydes, and epoxy resins, urea resins, and urethane resins obtained by adding a curing agent to an oligomer having a reactive epoxy group at the terminal can be suitably used. These resins may be used alone or as a mixture of two or more, and are mainly combined with the fiber material (sheet material 2) by impregnation. The resin solution to be impregnated into the sheet material 2 may be any of an aqueous solution, a solvent varnish, an emulsion, and the like, or may be a method of spraying solid resin powder. Among these, it is preferable to use those dissolved or dispersed in water, alcohol, or the like from the viewpoint of cost and safety. Furthermore, various fillers such as lead stearate, dibutyltin dilaurate, carbon black, calcium carbonate, titanium white, mica, glass spheres, aluminum hydroxide, antimony oxide, tri (2,3 dibromopropyl) phosphate, fat A heat stabilizer, a reinforcing agent, a flame retardant, an antistatic agent, and the like are used in combination. As a catalyst required for the production of a phenol resin, alkylamine, ammonia, sodium hydroxide, barium hydroxide and the like are preferable. In particular, alkylamine and ammonia have higher molecular weights than the other two and have low hydration properties in terms of molecular structure, so that the water resistance after bonding is remarkably improved. At this time, the phenol resin is preferably dissolved or dispersed in water or alcohol so as to have a solid content of 20 to 75% from the viewpoint of easy impregnation. When alcohol is used, it has a low boiling point and is easy to dry.
Is preferred. If the solid content is less than 20%, it becomes difficult to impregnate the required amount, and if it is more than 75%, the impregnation becomes difficult due to an increase in viscosity. The resin to be impregnated into the sheet material 2 contains 50% or more of a fiber ratio (weight ratio), and desirably 100 to 300%. When the sheet material 2 is impregnated, the solid content is 50 to 500 g / m 2 , preferably 1 to 500 g / m 2 .
It is preferable that the amount be 50 to 350 g / m 2 . If it is less than 50 g / m 2, it is difficult to exhibit sufficient scratch resistance, and if it is less than 500 g / m 2 , it takes a long curing time,
There is also a problem in appearance such as protruding from the end.
【0011】上述の如くシート材2に樹脂溶液を含浸さ
せた後、一定条件下で乾燥させて樹脂を半硬化状態にす
る。すなわちプリプレグ化する。プリプレグは、繊維補
強材と熱硬化性樹脂、その他必要に応じ熱可塑性樹脂,
着色剤,硬化触媒等を混和してなる強化プラスチック
の、接着性と成形性の能力を残した硬化終了前の半硬化
状態の成形素材であり、好ましいゲルタイムは150℃
で30〜800秒である。After impregnating the sheet material 2 with the resin solution as described above, the sheet material 2 is dried under a certain condition to bring the resin into a semi-cured state. That is, the prepreg is formed. Pre-preg is made of fiber reinforced material and thermosetting resin, other thermoplastic resin if necessary,
This is a semi-cured molding material before the completion of curing, which is a reinforced plastic obtained by admixing a coloring agent, a curing catalyst, etc., while maintaining the adhesiveness and moldability. The preferred gel time is 150 ° C.
30 to 800 seconds.
【0012】シート材2に含浸させた熱硬化性樹脂を、
含浸後半硬化状態にするための乾燥条件として、プリプ
レグ状態の溶媒含有率を3〜15重量%、さらには5〜
10重量%にすることが好ましく、3重量%未満では基
材1との接着不良をおこし、15重量%以下でない場合
は、プリプレグ同士ブロッキングをおこす。90〜12
0℃の温度で乾燥時間2.5〜20分で好ましい半硬化
状態のプリプレグを得ることができる。The thermosetting resin impregnated in the sheet material 2 is
As the drying conditions for setting the cured state in the latter half of the impregnation, the solvent content in the prepreg state is 3 to 15% by weight, more preferably 5 to 15% by weight.
The content is preferably set to 10% by weight, and if it is less than 3% by weight, poor adhesion to the substrate 1 is caused, and if it is not less than 15% by weight, blocking between prepregs is caused. 90-12
A preferable semi-cured prepreg can be obtained at a temperature of 0 ° C. and a drying time of 2.5 to 20 minutes.
【0013】プリプレグの引張強度としては、十分な耐
傷性発現のためには、破断強度10kgf以上であるこ
とが好ましい。10kgf未満では十分な耐傷性が発現
しない。破断強度の測定は、プリプレグを2枚の離型紙
間に挟み、150℃、5分、10kgf/cm2 の条件下
で熱プレスして樹脂を硬化させた後のものについて行っ
た。[0013] The tensile strength of the prepreg is preferably 10 kgf or more in order to sufficiently develop scratch resistance. If it is less than 10 kgf, sufficient scratch resistance is not exhibited. The measurement of the breaking strength was performed after the prepreg was sandwiched between two release papers and the resin was cured by hot pressing at 150 ° C. for 5 minutes under a condition of 10 kgf / cm 2 .
【0014】上述のようにしてシート材2に半硬化状態
の熱硬化性樹脂を含浸させたプリプレグを基材1上に重
ね合わせ、熱プレスする場合の条件としては、温度13
0℃〜180℃が好ましく、さらには140〜160℃
が好ましい。130℃より低いと樹脂の硬化が充分でな
く、180℃より高いと樹脂の硬化が速すぎて基材1と
の接触が不十分となり、かつ基材1の反りも大きくなっ
てしまうためである。また、圧力としては、1〜20k
gf/cm2 が好ましく、さらに好ましくは5〜15kg
f/cm2 であり、1kgf/cm2 より低いと樹脂の基材
1へのしみ出しが充分でないために接着力が低下し、2
0kgf/cm2 より大きいと基材1の反りが大きくなる
等の不都合が生ずる。さらにまた、プレス時間として
は、2.5〜20分間が好ましく、さらに好ましくは3
〜12.5分である。2.5分より短いと樹脂の硬化が
充分ではなく、20分より長いと樹脂の劣化が生じ、基
材1の反りも大きくなる。As described above, when the prepreg, in which the sheet material 2 is impregnated with the thermosetting resin in a semi-cured state, is overlaid on the base material 1 and hot pressed, the conditions are as follows.
0 ° C. to 180 ° C. is preferred, and 140 ° C. to 160 ° C.
Is preferred. If the temperature is lower than 130 ° C., the curing of the resin is not sufficient, and if the temperature is higher than 180 ° C., the curing of the resin is too fast, the contact with the substrate 1 becomes insufficient, and the warpage of the substrate 1 increases. . The pressure is 1 to 20 k
gf / cm 2 is preferable, and more preferably 5 to 15 kg.
f / cm 2 , and if it is lower than 1 kgf / cm 2 , the resin will not sufficiently exude to the base material 1 and the adhesive strength will be reduced.
If it is greater than 0 kgf / cm 2, problems such as an increase in the warpage of the substrate 1 occur. Further, the pressing time is preferably 2.5 to 20 minutes, more preferably 3 to 20 minutes.
~ 12.5 minutes. If the time is shorter than 2.5 minutes, the curing of the resin is not sufficient, and if the time is longer than 20 minutes, the resin is deteriorated and the warpage of the substrate 1 is increased.
【0015】ガラス繊維を含む織布又は不織布を単独で
シート材2とし、これに半硬化状態の熱硬化性樹脂を含
浸させたもの(プリプレグ)を単独で用いず、例えば紙
に熱硬化性樹脂を含浸させたものに上記プリプレグを貼
り合わせたものを用いることもできる。例えば、未硬化
のフェノール樹脂を紙に含浸させ、これに上記プリプレ
グを貼り合わせたものを用いれば全体の強度や寸法安定
性が飛躍的に向上する。A woven or non-woven fabric containing glass fibers is used alone as the sheet material 2, and a material impregnated with a semi-cured thermosetting resin (prepreg) is not used alone. Can also be used. For example, if the uncured phenol resin is impregnated into paper and the prepreg is bonded to the paper, the overall strength and dimensional stability are dramatically improved.
【0016】上述したように部材10を製造したなら
ば、化粧材4を尿素・メラミン系等の接着剤でシート材
2に接着する。化粧材4としては、木質系薄板である突
き板,紙,不織布,織布,塩化ビニル等の合成樹脂シー
トが好適に使用でき、厚さは1mm程度を超えないものが
よい。紙としては、木目を印刷したもので木目に沿って
凹凸加工が施されたものは、質感が高く、使用に好適で
ある。After the member 10 is manufactured as described above, the decorative material 4 is bonded to the sheet material 2 with an adhesive such as urea / melamine. As the decorative material 4, a veneer made of a thin wooden board, paper, a nonwoven fabric, a woven fabric, a synthetic resin sheet such as vinyl chloride or the like can be suitably used, and a material having a thickness not exceeding about 1 mm is preferable. As the paper, one printed with wood grain and subjected to unevenness processing along the wood grain has a high texture and is suitable for use.
【0017】熱プレスして硬化後の熱硬化性樹脂3は、
シート材2の全部に含浸することが好ましく、基材1に
は基材1の厚さが薄いときは全部、厚いときは一部に含
浸することとなる。The thermosetting resin 3 which has been hardened by hot pressing is:
It is preferable that the entirety of the sheet material 2 is impregnated. The base material 1 is impregnated entirely when the thickness of the base material 1 is thin, and partially when the thickness of the base material 1 is thick.
【0018】図2は、基材1の周囲に本実加工5,6を
施したものを示し、フローリングとして好適に使用でき
るものである。FIG. 2 shows the actual processing 5 and 6 applied to the periphery of the substrate 1, which can be suitably used as flooring.
【0019】基材1として厚さ12mmの合板を用い、化
粧材4として厚さ0.3mmの楢単板を用い、繊維長3mm
のガラス繊維からなる坪量100g/m2 の不織布をシ
ート材2とし、ガラス繊維の重量比で50%のフェノー
ル樹脂をシート材2に含浸させたプリプレグを用いて図
2に示すフローリングを製造し、これを実施例1とし
た。ガラス繊維の繊維長12mmでその他の条件は実施例
1と全く同一としたものを実施例2とし、実施例1のフ
ェノール樹脂を150%としたものを実施例3とし、実
施例2のフェノール樹脂を150%としたものを実施例
4とし、実施例4のフェノール樹脂を300%としたも
のを実施例5とした。また、基材1(厚さ12mmの合
板)に直接化粧材4として、厚さ0.3mmの楢単板を尿
素・メラミン系の接着剤で接着したものを比較例とし
た。A plywood having a thickness of 12 mm was used as the base material 1, a veneer veneer having a thickness of 0.3 mm was used as the decorative material 4, and a fiber length of 3 mm
The nonwoven fabric having a basis weight of 100 g / m 2 made of the above glass fiber was used as the sheet material 2, and the flooring shown in FIG. This was designated as Example 1. Example 2 was a glass fiber having a fiber length of 12 mm and the other conditions were completely the same as in Example 1, and Example 3 was a case where the phenol resin of Example 1 was 150%, and Example 3 was a phenol resin of Example 2. Was set as 150%, and Example 5 was set as the phenol resin of Example 4 with 300%. A comparative example was obtained by directly bonding a 0.3 mm thick oak veneer with a urea-melamine adhesive as a decorative material 4 directly to the base material 1 (12 mm thick plywood).
【0020】これら実施例1ないし5と比較例に対しJ
IS K−5400に基づき鉛筆のひっかき値をテスト
するとともに、直径6.35mm、重量150gの球を3
cmの高さから50回落下させたのちの凹み穴径を測定す
るテスト(落球試験 JISA−1408)を行った。
その結果は次の表1に示す通りであった。鉛筆ひっかき
値において評価が「H」は×、「2H」は△、「3H」
は○、「4H以上」は◎として評価した。また、落球試
験において凹み穴の径が5mm以上は×、4mm〜5mm未満
は△、3mm〜4mm未満は○、3mm未満は◎として評価し
た。In Examples 1 to 5 and Comparative Example, J
The scratch value of the pencil was tested according to IS K-5400, and a ball having a diameter of 6.35 mm and a weight of 150 g
A test (drop test JISA-1408) for measuring the diameter of the pit after dropping 50 times from the height of cm was performed.
The results were as shown in Table 1 below. In the pencil scratch value, "H" is evaluated as "X", "2H" is evaluated as "△", and "3H".
Was evaluated as ○, and “4H or more” was evaluated as ◎. In the ball drop test, the diameter of the pit was 5 mm or more, x: 4 mm to less than 5 mm, ○: 3 mm to less than 4 mm, ○: less than 3 mm.
【0021】[0021]
【表1】 [Table 1]
【0022】[0022]
【発明の効果】以上説明したように、この発明によれ
ば、基材上にガラス繊維を含むシート材を重ね合わせ、
基材とシート材の両者の全体又は一部に熱硬化性樹脂を
含浸させて互いに接着し、シート材上に化粧材を貼着し
たので、化粧材の下層に硬質な層が形成されるので、耐
傷性を向上させ、しかも安価かつ容易に製造することが
できる。また、温度や湿度の変化に対してもシートの存
在により寸法安定性に優れ、強度面でも向上する。As described above, according to the present invention, a sheet material containing glass fibers is overlaid on a base material,
Since the whole or part of both the base material and the sheet material is impregnated with the thermosetting resin and adhered to each other, and the decorative material is stuck on the sheet material, a hard layer is formed under the decorative material. In addition, the scratch resistance can be improved, and it can be manufactured inexpensively and easily. Also, the presence of the sheet provides excellent dimensional stability against changes in temperature and humidity, and improves strength.
【図1】この発明の好適な実施例を示す断面図。FIG. 1 is a sectional view showing a preferred embodiment of the present invention.
【図2】他の実施例を示す説明図。FIG. 2 is an explanatory view showing another embodiment.
1 基材 2 シート材 3 熱硬化性樹脂 4 化粧材 Reference Signs List 1 base material 2 sheet material 3 thermosetting resin 4 cosmetic material
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI E04C 2/24 E04C 2/24 Q E04F 13/08 E04F 13/08 A ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI E04C 2/24 E04C 2/24 Q E04F 13/08 E04F 13/08 A
Claims (4)
ね合わせ、 基材とシート材の両者の全体又は一部に熱硬化性樹脂を
含浸させて互いに接着し、 シート材上に化粧材を貼着したことを特徴とする積層仕
上材。1. A sheet material containing glass fiber is superimposed on a base material, and both or a part of the base material and the sheet material are impregnated with a thermosetting resin and adhered to each other, and a decorative material is formed on the sheet material. Laminated finishing material characterized by having affixed thereto.
キシ樹脂,ウレタン樹脂,ユリア樹脂のいずれか単独又
は2以上の混合物であることを特徴とする請求項1に記
載の積層仕上材。2. The laminated finishing material according to claim 1, wherein the thermosetting resin is any one of phenol resin, epoxy resin, urethane resin and urea resin, or a mixture of two or more thereof.
特徴とする請求項1又は2に記載の積層仕上材。3. The laminated finishing material according to claim 1, wherein the base material is paper or wood-based material.
化ビニル等の合成樹脂シートのいずれかであることを特
徴とする請求項1ないし3のいずれか1項に記載の積層
仕上材。4. The laminated finish according to claim 1, wherein the decorative material is any one of a veneer made of a thin wooden board, paper, and a synthetic resin sheet such as vinyl chloride. Wood.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24189797A JPH10114021A (en) | 1996-08-23 | 1997-08-22 | Laminated finishing material |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24106096 | 1996-08-23 | ||
JP8-241060 | 1996-08-23 | ||
JP24189797A JPH10114021A (en) | 1996-08-23 | 1997-08-22 | Laminated finishing material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10114021A true JPH10114021A (en) | 1998-05-06 |
Family
ID=26535058
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24189797A Pending JPH10114021A (en) | 1996-08-23 | 1997-08-22 | Laminated finishing material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10114021A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007077726A (en) * | 2005-09-16 | 2007-03-29 | Dainippon Printing Co Ltd | Flooring |
JP2007077763A (en) * | 2005-09-16 | 2007-03-29 | Dainippon Printing Co Ltd | Flooring |
JP2009202376A (en) * | 2008-02-26 | 2009-09-10 | Panasonic Electric Works Co Ltd | Fibre board and manufacturing method of decorative material |
-
1997
- 1997-08-22 JP JP24189797A patent/JPH10114021A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007077726A (en) * | 2005-09-16 | 2007-03-29 | Dainippon Printing Co Ltd | Flooring |
JP2007077763A (en) * | 2005-09-16 | 2007-03-29 | Dainippon Printing Co Ltd | Flooring |
JP2009202376A (en) * | 2008-02-26 | 2009-09-10 | Panasonic Electric Works Co Ltd | Fibre board and manufacturing method of decorative material |
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