JPH02223441A - Manufacture of decorative laminate - Google Patents
Manufacture of decorative laminateInfo
- Publication number
- JPH02223441A JPH02223441A JP23308088A JP23308088A JPH02223441A JP H02223441 A JPH02223441 A JP H02223441A JP 23308088 A JP23308088 A JP 23308088A JP 23308088 A JP23308088 A JP 23308088A JP H02223441 A JPH02223441 A JP H02223441A
- Authority
- JP
- Japan
- Prior art keywords
- emulsion
- adhesive
- thermosetting
- decorative
- layer
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 239000000839 emulsion Substances 0.000 claims abstract description 32
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 32
- 239000000853 adhesive Substances 0.000 claims abstract description 31
- 230000001070 adhesive effect Effects 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000004202 carbamide Substances 0.000 claims abstract description 8
- 239000002245 particle Substances 0.000 claims abstract description 8
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 6
- 239000000057 synthetic resin Substances 0.000 claims abstract description 6
- 239000011094 fiberboard Substances 0.000 claims abstract description 4
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 4
- 150000003839 salts Chemical class 0.000 claims abstract description 3
- 239000000758 substrate Substances 0.000 claims description 18
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 239000002023 wood Substances 0.000 abstract description 12
- 239000010410 layer Substances 0.000 abstract description 10
- 239000012790 adhesive layer Substances 0.000 abstract description 7
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 238000003825 pressing Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract 1
- 230000035939 shock Effects 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 239000000123 paper Substances 0.000 description 12
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 7
- 229920001807 Urea-formaldehyde Polymers 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000010936 titanium Substances 0.000 description 7
- 229910052719 titanium Inorganic materials 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 101100228790 Schizosaccharomyces pombe (strain 972 / ATCC 24843) yip11 gene Proteins 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- UJVRJBAUJYZFIX-UHFFFAOYSA-N nitric acid;oxozirconium Chemical compound [Zr]=O.O[N+]([O-])=O.O[N+]([O-])=O UJVRJBAUJYZFIX-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000007261 regionalization Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、化粧板の製造方法に関するものである。[Detailed description of the invention] [Industrial application field] The present invention relates to a method for manufacturing decorative laminates.
[従来技術とその欠点]
従来、この種の化粧板の製造方法において、パーティク
ルボード等の木質基板の上にロールコータ等のスペレッ
ダーで常用接着剤を塗布した後、化粧シートを載置し、
ロールプレスや平板プレス等で加圧接着して化粧板を製
造していた。[Prior Art and Its Disadvantages] Conventionally, in the manufacturing method of this type of decorative board, a common adhesive is applied onto a wooden substrate such as a particle board using a spreader such as a roll coater, and then a decorative sheet is placed.
Decorative boards were manufactured by bonding under pressure using a roll press or flat plate press.
しかしながら、上記化粧板をランニングソー等の鋸でカ
ットした時、鋸の衝撃で化粧板の側端部が欠ける(以下
、木端欠けと称す)という問題を生じていた。とりわけ
、50g/m2以下の薄い化粧紙を用いて貼着した場合
、木端欠けが顕著に現れていた。However, when the decorative board is cut with a saw such as a running saw, the impact of the saw causes the side edges of the decorative board to chip (hereinafter referred to as wood edge chipping). Particularly, when a thin decorative paper of 50 g/m 2 or less was used for pasting, chipping of wood edges was noticeable.
[発明の目的コ
本発明は、上記木端欠けを解消し、加えてエンボス加工
によるエンボスも明瞭に入るようにすることを目的とす
る。[Object of the Invention] The object of the present invention is to eliminate the above-mentioned chipping of the wood end, and also to enable the embossing to be clearly embossed.
[発明の構成]
本発明は、パーティクルボードやファイバーボード等の
木質基板に熱硬化型エマルジョンを塗布し乾燥させた後
に、尿素・酢酸ビニル系合成樹脂、尿素系合成樹脂、尿
素・メラミン系合成樹脂、酢酸ビニル系合成樹脂等を上
記熱硬化型エマルジョンの上に塗布し、次いで化粧シー
トを載置し、加圧接着して所望の化粧板を製造する方法
である。[Structure of the Invention] The present invention applies a thermosetting emulsion to a wooden substrate such as a particle board or a fiberboard and then dries it. In this method, a vinyl acetate-based synthetic resin or the like is applied onto the thermosetting emulsion, and then a decorative sheet is placed and bonded under pressure to produce a desired decorative board.
上記木質基板としては、パーティクルボードやファイバ
ーボード等木質繊維や木粉あるいは木材チップを用いた
ボードが挙られる。また、上記熱硬化型エマルジョンと
して、たとえば、酢酸ビニルに反応性モノマーであるエ
チレングリコールジアクリレート、N−メチロールアク
リルアミド、メチロールメタクリルアミド、あるいはこ
れらをエーテル化したアルコキシメチロールメタクリル
アミドのような反応性モノマーを共重合させた耐熱性の
ある熱硬化型エマルジョンが望ましい。さらに、ポバー
ル、アクリル酸やアクリル酸エチル等のアクリル酸エチ
ル、あるいは酢酸ビニル・アクリル系の樹脂にN−メチ
ロールアクリルアミドを共重合させてえられたエマルジ
ョン、若しくは、酢酸ビニル樹脂や尿素・酢酸ビニル樹
脂等に金属塩、たとえば、硝酸ジルコニルあるいは塩化
亜鉛などを添加して耐熱性を向上させた熱硬化型エマル
ジョンでもよい。上記種々の熱硬化型エマルジョンのガ
ラス転移温度(以下、Tgと記す)は、70°C以上の
温度範囲に入ることが必要となる。70℃未満のTgを
有する熱硬化型エマルジョンでは、後述の加熱圧締時の
熱により接着不良(俗にパンクと称す現象)を生じるの
で好ましくない。Examples of the wood substrate include boards using wood fibers, wood powder, or wood chips, such as particle board and fiberboard. In addition, as the thermosetting emulsion, for example, reactive monomers such as ethylene glycol diacrylate, N-methylol acrylamide, methylol methacrylamide, or alkoxymethylol methacrylamide, which is an etherification of these, may be added to vinyl acetate. A copolymerized, heat-resistant thermosetting emulsion is desirable. Furthermore, poval, acrylic acid, ethyl acrylate such as ethyl acrylate, emulsion obtained by copolymerizing N-methylolacrylamide with vinyl acetate/acrylic resin, vinyl acetate resin, urea/vinyl acetate resin, etc. A thermosetting emulsion with improved heat resistance by adding a metal salt such as zirconyl nitrate or zinc chloride to the emulsion may also be used. The glass transition temperature (hereinafter referred to as Tg) of the various thermosetting emulsions described above is required to be in a temperature range of 70°C or higher. A thermosetting emulsion having a Tg of less than 70° C. is not preferable because it causes adhesion failure (a phenomenon commonly referred to as puncture) due to the heat generated during heating and pressing as described below.
上述した熱硬化型エマルジョンを木質基板に塗布した後
、遠赤外線や熱風などの手段で強制乾燥させた後、更に
尿素φ酢酸ビニル系合成樹脂接着剤等を木質基板に塗布
する。ここで塗布量は、20〜100 gem2の範囲
が好ましく、この塗布量が過多あるいは過少であると接
着不良の原因となり不適当である。上記接着剤が塗布さ
れた木質基板の上に化粧シート、たとえばチタン紙、混
抄紙、樹脂含浸紙などを載置し、加圧接着して化粧板を
得る。上記尿素・酢酸ビニル系合成樹脂接着剤は、木質
基板の上に塗布することのほか、上記化粧シートの裏側
に塗布してもよいし、あるいは、木質基板の上と化粧シ
ートの裏面の両方に塗布してもよいことは言うまでもな
い。After the above-mentioned thermosetting emulsion is applied to a wooden substrate, it is forcedly dried by means such as far infrared rays or hot air, and then a urea φ vinyl acetate-based synthetic resin adhesive or the like is further applied to the wooden substrate. The coating amount is preferably in the range of 20 to 100 gem2, and if the coating amount is too large or too small, it will cause poor adhesion and is inappropriate. A decorative sheet, such as titanium paper, mixed paper, resin-impregnated paper, etc., is placed on the wooden substrate coated with the adhesive and bonded under pressure to obtain a decorative board. In addition to applying the above-mentioned urea/vinyl acetate-based synthetic resin adhesive onto the wooden substrate, it may also be applied to the back side of the above-mentioned decorative sheet, or alternatively, to both the top of the wooden substrate and the back side of the decorative sheet. Needless to say, it may be applied by coating.
上述した方法によって、木端欠けの起こらない化粧板を
得ることができるわけである。すなわち、木質基板の上
に尿素樹脂接着剤等の熱硬化性樹脂接着剤を塗布するの
みでは、接着剤が硬すぎるために鋸の衝撃によって接着
剤の下側の基板のチップ等が欠落する、いわゆる木端欠
けが起こり、また、酢酸ビニル樹脂エマルジョン等の熱
可塑性樹脂接着剤の塗布のみでは、この熱可塑性樹脂接
着剤固有の可撓性によって木端欠けは改善することがで
きるが、仕上った化粧板の表面硬度や紙間強度が劣ると
いう問題は依然として残る。そこで、上記2つの事情に
鑑みて本発明に係る熱硬化型エマルジョン接着剤を木質
基板に塗布して木質基板表面上に熱硬化型エマルジョン
層を形成し、さらに、その上に熱硬化性樹脂接着剤層を
形成し、化粧シートを加圧接着して木端欠けの起こらな
い化粧板を得ることができる。By the method described above, it is possible to obtain a decorative board that does not suffer from wood edge chipping. In other words, simply applying a thermosetting resin adhesive such as a urea resin adhesive onto a wooden substrate will cause the adhesive to be too hard and cause chips, etc. on the substrate underneath the adhesive to come off due to the impact of the saw. So-called wood end chipping occurs, and wood end chipping can be improved by simply applying a thermoplastic resin adhesive such as vinyl acetate resin emulsion due to the inherent flexibility of this thermoplastic resin adhesive. The problem of poor surface hardness and paper-to-paper strength of decorative boards still remains. Therefore, in view of the above two circumstances, the thermosetting emulsion adhesive according to the present invention is applied to a wooden substrate to form a thermosetting emulsion layer on the surface of the wooden substrate, and then a thermosetting resin adhesive is applied on top of the thermosetting emulsion layer. By forming an adhesive layer and adhering a decorative sheet under pressure, a decorative board that does not cause wood edge chipping can be obtained.
また、常用接着剤を1回塗布した後、化粧シーI・を載
置し加圧接着しながらエンボス加工を施した化粧板では
、木質基板表面への上記接着剤の吸い込みむらで接着剤
層自体に厚みむらが生じるため、上記エンボス形状が均
一となりにくい。勢硬化型エマルジョンは、架橋密度が
尿素樹脂等の熱硬化性樹脂の接着剤のそれよりも小さい
ため、それ相応の熱可塑性を有し、18以上の温度で加
熱圧締すると熱による凹凸状のエンボス模様形成が期待
できる。さらに、本発明では、上記熱硬化型エマルジョ
ン層が乾燥してその上から水性熱硬化性樹脂接着剤を塗
布するので、この接着剤中の水分が可塑剤として作用し
、上記熱による凹凸状のエンボス模様形成が助長される
。In addition, with decorative boards that are embossed while applying a common adhesive once and then placing a decorative sheet I and adhering under pressure, the adhesive layer itself may be unevenly sucked into the surface of the wooden substrate. Since thickness unevenness occurs, it is difficult to obtain a uniform embossed shape. Since the crosslinking density of the thermosetting emulsion is lower than that of adhesives made of thermosetting resins such as urea resin, it has corresponding thermoplasticity, and when heated and pressed at a temperature of 18 or higher, it will not cause unevenness due to heat. Formation of embossed patterns can be expected. Furthermore, in the present invention, since the thermosetting emulsion layer is dried and a water-based thermosetting resin adhesive is applied thereon, the moisture in this adhesive acts as a plasticizer, and the unevenness caused by the heat is reduced. Embossed pattern formation is encouraged.
このように、本発明では、乾燥・硬化した熱硬化型エマ
ルジョン層の上に常用の熱硬化性樹脂接着剤の層が形成
されるため、上記常用接着剤の木質基板への浸透が阻止
され均一な厚みの接着剤層が維持される。よって、化粧
シートを上記接着剤層の1−に載置し熱圧締する際、均
一なかつ明瞭なエンボス形状を有する化粧板を得ること
ができる。In this way, in the present invention, since a layer of a commonly used thermosetting resin adhesive is formed on the dried and hardened thermosetting emulsion layer, the penetration of the commonly used adhesive into the wooden substrate is prevented and the adhesive is uniformly coated. The thickness of the adhesive layer is maintained. Therefore, when the decorative sheet is placed on the adhesive layer 1- and heat-pressed, a decorative sheet having a uniform and clear embossed shape can be obtained.
ただ、予め表面硬度や紙間強度を改善したFFシート(
ハードコート紙)を木質基板に加圧接着する場合、上記
熱硬化性樹脂接着剤層の変りに酢酸ビニル樹脂エマルシ
ョン等の熱+if塑性樹脂接着剤も用いることができる
。However, FF sheets with improved surface hardness and interpaper strength (
When adhesively bonding (hard coated paper) to a wooden substrate under pressure, a thermo+if plastic resin adhesive such as a vinyl acetate resin emulsion can also be used instead of the thermosetting resin adhesive layer.
[発明の効果コ
上述したように、本発明は、木質基板の上にます熱硬化
型エマルジョン層を形成し、次いでその上に熱硬化性接
着剤等の常用接着剤層を形成し、そのEに化粧シートを
載置し加圧接着して化粧板を得るので、鋸の衝撃によっ
て化粧板の側端部が欠ける、いわゆる木端欠けが起こら
ない。さらに、1−記化粧板の中に用いられている常用
接着剤が熱硬化性樹脂接着剤であるので、化粧シートの
接着に加えて化粧シート内に浸透し、表面硬度や紙間強
度も向」ニする。また、発明の構成の欄で述べたように
、熱硬化型エマルジョン層の個々の性質により、熱圧締
してエンボス加工を施すとこのエンボス形状も明瞭にし
かも均一に施された化粧板を得ることができる。[Effects of the Invention] As described above, the present invention involves forming a thermosetting emulsion layer on a wooden substrate, then forming a common adhesive layer such as a thermosetting adhesive thereon, and Since the decorative sheet is placed on the board and bonded under pressure to obtain the decorative board, the side edges of the decorative board will not be chipped due to the impact of the saw, so-called wood edge chipping. Furthermore, since the commonly used adhesive used in the decorative board described in 1-1 is a thermosetting resin adhesive, in addition to adhering the decorative sheet, it also penetrates into the decorative sheet and improves surface hardness and interpaper strength. ” In addition, as mentioned in the section of the structure of the invention, due to the individual properties of the thermosetting emulsion layer, when heat-pressed and embossed, a decorative board with a clearly and uniformly embossed shape can be obtained. be able to.
[実施例1]
15tmのパーティクルボードにロールスプレ・、ダ一
でN−メチロールアクリルアミド変性酢酸ビニルエマル
ジョンを40g/m2Pha布し、遠赤外線加熱方式に
よって乾燥させた後、その上に尿素・酢酸ビニル系樹脂
接着剤を50g/m2塗布し、さらにその上にチタン紙
(30g/m2 )を載置・積層し、140°C915
Kgf/mノ、 25秒熱圧し、所望の化粧板を得た。[Example 1] 40g/m2Pha of N-methylolacrylamide-modified vinyl acetate emulsion was applied to a 15tm particle board by roll spray and die, and after drying by far infrared heating method, urea/vinyl acetate emulsion was applied on top of it. 50g/m2 of resin adhesive was applied, and titanium paper (30g/m2) was placed and laminated on top of it, and heated at 140°C915
A desired decorative board was obtained by hot pressing at Kgf/m for 25 seconds.
[実施例2]
実施例1において、チタン紙(50g/m2)を用い、
圧締時間を30秒にするほか同じ方法で所望の化粧板を
得た。[Example 2] In Example 1, using titanium paper (50 g/m2),
A desired decorative board was obtained using the same method except that the pressing time was changed to 30 seconds.
[実施例3]
実施例1において、N−メチロールアクリルアミド変性
酢酸ビニルエマルジョンを20g/m2塗布しチタン紙
(30g/m?)の裏面に尿素樹脂を40g/m2塗布
した後、そのチタン紙を15m+nパーティクルボード
に積層し、梨地エンボス加工を施すほか同じ方法で所望
の化粧板を得た。[Example 3] In Example 1, 20 g/m2 of N-methylolacrylamide-modified vinyl acetate emulsion was applied and 40 g/m2 of urea resin was applied to the back side of titanium paper (30 g/m?), and then the titanium paper was heated to 15 m+n. The desired decorative board was obtained by the same method except for laminating it on particle board and applying matte embossing.
[実施例4コ
実施例1において、熱硬化型エマルジョンとして耐熱性
のある硝酸ジルコニル変性酢酸ビニルエマルジョンを5
0g/B2塗布し乾燥させ、さらにその上に、尿素・メ
ラミン系熱硬化性樹脂接着剤を20g/m2塗布し、梨
地エンホス加、゛Lを施すほか同じ方法で所望の化粧板
を得た。[Example 4] In Example 1, a heat-resistant zirconyl nitrate-modified vinyl acetate emulsion was used as a thermosetting emulsion.
0g/B2 was coated and dried, and then a urea/melamine thermosetting resin adhesive was coated at 20g/m2, and a desired decorative board was obtained in the same manner except for satin finish enhancement and L.
[比較例1]
15mmのパーティクルボードに尿素樹脂90g/mz
を塗布し乾燥させ、次いでチタン紙(30g/m’)を
積層し、次いで140°0 、15Kgf/ml、 2
5秒熱圧し、化粧板を得た。[Comparative Example 1] Urea resin 90g/mz on 15mm particle board
was coated and dried, then laminated with titanium paper (30g/m'), then 140°0, 15Kgf/ml, 2
A decorative board was obtained by hot pressing for 5 seconds.
[比較例2]
比較例1において、尿素樹脂90g/m7の代わりに尿
素・酢酸ビニル系樹脂90g/m7、チタン紙の坪量を
30g/m’から5(Ig/m2に変更し、圧締時間を
30秒にするほか同じ方法で化粧板を得た。[Comparative Example 2] In Comparative Example 1, 90 g/m of urea/vinyl acetate resin was used instead of 90 g/m of urea resin, the basis weight of titanium paper was changed from 30 g/m' to 5 (Ig/m2), and the urea resin was changed to 5 (Ig/m2). A decorative board was obtained in the same manner except that the time was changed to 30 seconds.
[比較例3J
比較例1において、尿素樹脂80g/m2をハードボー
ドに塗布し、梨地エンボス加工を施すほか同じ方法でエ
ンボス化粧板を得た。[Comparative Example 3J In Comparative Example 1, 80 g/m2 of urea resin was applied to a hardboard, and an embossed decorative board was obtained in the same manner except that it was embossed with a satin finish.
「比較試験」
」−記各々実施例、比較例で得た化粧板の表面性状をみ
た。その結果は、次のとおりである。"Comparative Test" - The surface properties of the decorative laminates obtained in Examples and Comparative Examples were examined. The results are as follows.
Claims (2)
基板に接着剤を介して化粧シートを加圧接着して得られ
る化粧板の製造方法において、上記木質基板の表面に熱
硬化型エマルジョンを塗布し乾燥させた後、尿素・酢酸
ビニル系合成樹脂接着剤等の常用接着剤を上記化粧シー
トとの間に介することを特徴とする化粧板の製造方法。(1) In a method for manufacturing a decorative board obtained by pressure-bonding a decorative sheet to a wooden substrate such as particle board or fiberboard using an adhesive, a thermosetting emulsion is applied to the surface of the wooden substrate and dried. After that, a commonly used adhesive such as a urea/vinyl acetate based synthetic resin adhesive is interposed between the decorative sheet and the decorative sheet.
金属塩を添加したものを用いることを特徴とする請求項
1記載の化粧板の製造方法。(2) The method for manufacturing a decorative board according to claim 1, characterized in that the thermosetting emulsion is a thermoplastic resin to which a metal salt is added.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23308088A JPH02223441A (en) | 1988-09-17 | 1988-09-17 | Manufacture of decorative laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23308088A JPH02223441A (en) | 1988-09-17 | 1988-09-17 | Manufacture of decorative laminate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02223441A true JPH02223441A (en) | 1990-09-05 |
Family
ID=16949488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23308088A Pending JPH02223441A (en) | 1988-09-17 | 1988-09-17 | Manufacture of decorative laminate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02223441A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5019294A (en) * | 1973-06-22 | 1975-02-28 | ||
JPS5070509A (en) * | 1973-10-31 | 1975-06-12 | ||
JPS5299204A (en) * | 1976-02-18 | 1977-08-19 | Sumitomo Bakelite Co | Surfaceereinforced plywood |
JPS5844474A (en) * | 1981-09-11 | 1983-03-15 | Ricoh Co Ltd | Transfer paper peeling device of fixing device |
JPS63183841A (en) * | 1987-01-26 | 1988-07-29 | 松下電工株式会社 | Manufacture of printed decorative flitch |
-
1988
- 1988-09-17 JP JP23308088A patent/JPH02223441A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5019294A (en) * | 1973-06-22 | 1975-02-28 | ||
JPS5070509A (en) * | 1973-10-31 | 1975-06-12 | ||
JPS5299204A (en) * | 1976-02-18 | 1977-08-19 | Sumitomo Bakelite Co | Surfaceereinforced plywood |
JPS5844474A (en) * | 1981-09-11 | 1983-03-15 | Ricoh Co Ltd | Transfer paper peeling device of fixing device |
JPS63183841A (en) * | 1987-01-26 | 1988-07-29 | 松下電工株式会社 | Manufacture of printed decorative flitch |
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