JPS63162239A - Manufacture of laminate with cured resin layer - Google Patents
Manufacture of laminate with cured resin layerInfo
- Publication number
- JPS63162239A JPS63162239A JP61311692A JP31169286A JPS63162239A JP S63162239 A JPS63162239 A JP S63162239A JP 61311692 A JP61311692 A JP 61311692A JP 31169286 A JP31169286 A JP 31169286A JP S63162239 A JPS63162239 A JP S63162239A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- base material
- thermosetting resin
- resin layer
- laminate
- 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
- 229920005989 resin Polymers 0.000 title claims description 56
- 239000011347 resin Substances 0.000 title claims description 56
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 239000000463 material Substances 0.000 claims description 41
- 229920001187 thermosetting polymer Polymers 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 8
- 238000010030 laminating Methods 0.000 claims description 6
- 238000003825 pressing Methods 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 14
- 238000000576 coating method Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 7
- 238000003475 lamination Methods 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 239000004800 polyvinyl chloride Substances 0.000 description 5
- 229920000915 polyvinyl chloride Polymers 0.000 description 5
- 239000004568 cement Substances 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000010440 gypsum Substances 0.000 description 4
- 229910052602 gypsum Inorganic materials 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000007756 gravure coating Methods 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920006337 unsaturated polyester resin Polymers 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- 229920009204 Methacrylate-butadiene-styrene Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 238000007754 air knife coating Methods 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920006284 nylon film Polymers 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005670 poly(ethylene-vinyl chloride) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、熱硬化性樹脂層付きのシートを板状の別の
基材上にラミネートする際などにラミネート時の熱を利
用して、熱硬化性樹脂層の硬化を行なう、硬化梼脂層を
存するラミネート体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 utilizes heat during lamination when laminating a sheet with a thermosetting resin layer onto another plate-shaped base material. The present invention relates to a method for producing a laminate having a cured resin layer, in which a thermosetting resin layer is cured.
従来、基材上に別の基材をラミネートし、その更に上に
熱硬化性樹脂層を形成する際には、予め上側になる基材
の表面に熱硬化性樹脂の未硬化層を設け、充分硬化させ
てから、下側になる基材とラミネートする方法がとられ
ている。Conventionally, when laminating another base material on top of another base material and forming a thermosetting resin layer on top of it, an uncured layer of thermosetting resin is previously provided on the surface of the upper base material. The method used is to allow the material to harden sufficiently and then laminate it with the underlying substrate.
しかし、熱硬化性樹脂層を硬化させるには高い温度と長
い時間を必要とし、しかも通常のコーター付属の乾燥装
置は単に乾燥を行なう目的で設けられているので、コー
ターを使用しただけでは充分な硬化が行なえず、逆に、
硬化を充分に行なおうとすると塗布速度が遅(なるため
に、塗料の乾燥性や粘度を大幅に変えなければならず、
コーターで塗布可能な塗料の性質の範囲を外れる。However, curing a thermosetting resin layer requires high temperatures and a long time, and the drying equipment that comes with a normal coater is provided solely for the purpose of drying, so using a coater alone is not sufficient. Hardening cannot be performed, and on the contrary,
If sufficient curing is to be achieved, the coating speed will be slow (this will require drastic changes in the drying properties and viscosity of the paint).
The properties of the paint that can be applied with a coater are outside the range.
また、硬化に高い温度と長い時間を必要とするために、
基材として耐熱性の低いもの、特に−aのプラスチック
フィルムは事実上、使用できない。Also, because it requires high temperature and long time for curing,
As a base material, materials with low heat resistance, especially plastic films of -a, cannot be used in practice.
従って、この発明で解決すべき点は、硬化樹脂層を有す
るラミネート体を製造する際に、従来、塗布工程を通常
のコーターとコーターに適した性質の塗料を使用して熱
硬化性樹脂を行なうことができない点である。Therefore, the problem to be solved by this invention is that when producing a laminate body having a cured resin layer, the coating process for thermosetting resin was conventionally carried out using a normal coater and a paint with properties suitable for the coater. This is something that cannot be done.
この発明では、ラミネートを熱を利用して行なわせ、そ
の際の熱を利用して、表面の熱硬化性樹脂層の硬化も行
なわせることにより、問題点の解消が可能になった。In this invention, the problem can be solved by laminating using heat and by using the heat at that time to also cure the thermosetting resin layer on the surface.
即ち、この発明は、
X1第1の基杓の一方の面には熱硬化性樹脂の未硬化層
を設け、その反対面側に第2の基材が来るようにして第
1、第2の基材を加熱および加圧することにより、第1
、第2の基材をラミ享−トすると共に第1の基材の一方
の面上の熱硬化性樹脂の未硬化層を硬化させることを特
徴とする硬化樹脂層を有するラミネート体の製造方法J
を要旨とするものである。That is, in the present invention, an uncured layer of thermosetting resin is provided on one surface of the first base ladle, and the first and second base materials are placed on the opposite surface thereof. By heating and pressurizing the base material, the first
A method for manufacturing a laminate having a cured resin layer, which comprises laminating a second base material and curing an uncured layer of thermosetting resin on one side of the first base material. J
The main points are as follows.
この発明では、予め熱硬化性樹脂を硬化させる替わりに
、前段階では硬化させず単に乾燥させて固化するにとど
め、次のラミネート時の熱を利用して硬化を行なわせる
方法を採用したことにより、塗布後長い時間をかけて加
熱する必要がない。また、塗布直後には硬化を行わず単
に乾燥するのみであるので、耐熱性の低い基材であって
も、熱変形にいたる程の過大な熱を受けない。In this invention, instead of curing the thermosetting resin in advance, it is simply dried and solidified without curing in the previous stage, and the curing is performed using the heat during the next lamination. , there is no need to heat it for a long time after application. Further, since the coating is simply dried without curing immediately after application, even a base material with low heat resistance will not receive excessive heat to the extent that it causes thermal deformation.
以下、この発明を実施例に基づいて具体的に説明する。 Hereinafter, this invention will be specifically explained based on examples.
玉且
この発明で用いる第1、第2の基材は、原則的には、次
のような素材からなる:
薄葉紙、晒クラフト紙、チタン紙、リンター紙、板紙、
石膏ボード紙などの紙、
ポリエチレンフィルム、ポリピロピレンフィルム、ポリ
塩化ビニルフィルム、ポリ塩化ビニリデンフィルム、ポ
リビニルアルコールフィルム、ポリエチレンテレフタレ
ートフィルム、ポリカーボネートフィルム、ナイロンフ
ィルム、ポリスチレンフィルム、エチレン−酢酸ビニル
共重合体フィルム、エチレン−ビニルアルコール共重合
体フィルム、アイオノマーなどのプラスチックフィルム
、または、これらプラスチックのシート、
プラスチックパネルとして、AAS樹脂、ABS樹脂、
AC3樹脂、アミノ樹脂、酢酸セルロース樹脂、酪酢酸
セルロース、エチルセルロースなどのセルロース樹脂、
アリル樹脂、エチレン−α−オレフィン共重合体、エチ
レン−酢酸ビニル−塩化ビニル共重合体、エチレン−塩
化ビニル共重合体、エチレン、酢酸ビニル共重合体、ア
イオノマー、MBS樹脂、メタクリル−スチレン共重合
体、ニトリル樹脂、フェノール樹脂、ポリアミド樹脂、
ポリアクリレート樹脂、ポリカーボネート樹脂、ポリブ
タジェン樹脂、ポリブチレンテレフタレート樹脂、ポリ
エチレン樹脂、ポリエチレンテレフタレート樹脂、ポリ
メチルメタクリレート樹脂、ポリプロピレン樹脂、ポリ
フェニレンオキシド樹脂、ポリスチレン樹脂、AS樹脂
、ポリウレタン樹脂、ポリ塩化ビニル樹脂、アクリル変
性ポリ塩化ビニル樹脂、不飽和ポリエステル樹脂などの
プラスチックのパネル、
木、合板、バーチクルボードなどの木質の基材、
石膏ボード、石膏スラグボードなどの石膏系基材、
パルプセメント板、石綿セメント板、木片セメント板な
どの繊維セメント板、
GRCおよびコンクリート、
鉄、アルミニウム、銅などの金属箔もしくはシート。The first and second base materials used in this invention are basically made of the following materials: tissue paper, bleached kraft paper, titanium paper, linter paper, paperboard,
Paper such as gypsum board paper, polyethylene film, polypropylene film, polyvinyl chloride film, polyvinylidene chloride film, polyvinyl alcohol film, polyethylene terephthalate film, polycarbonate film, nylon film, polystyrene film, ethylene-vinyl acetate copolymer film , ethylene-vinyl alcohol copolymer film, ionomer, or other plastic films, or sheets of these plastics.As plastic panels, AAS resin, ABS resin,
Cellulose resins such as AC3 resin, amino resin, cellulose acetate resin, cellulose butyrate acetate, ethyl cellulose,
Allyl resin, ethylene-α-olefin copolymer, ethylene-vinyl acetate-vinyl chloride copolymer, ethylene-vinyl chloride copolymer, ethylene, vinyl acetate copolymer, ionomer, MBS resin, methacrylic-styrene copolymer , nitrile resin, phenolic resin, polyamide resin,
Polyacrylate resin, polycarbonate resin, polybutadiene resin, polybutylene terephthalate resin, polyethylene resin, polyethylene terephthalate resin, polymethyl methacrylate resin, polypropylene resin, polyphenylene oxide resin, polystyrene resin, AS resin, polyurethane resin, polyvinyl chloride resin, acrylic modification Plastic panels such as polyvinyl chloride resin and unsaturated polyester resin, wood base materials such as wood, plywood and verticle board, gypsum base materials such as gypsum board and gypsum slag board, pulp cement board, asbestos cement board, Fiber cement boards such as wood cement boards, GRC and concrete, metal foils or sheets of iron, aluminum, copper etc.
上記の素材はいずれを第1、第2の基材に使用してもよ
いが、適用頻度の多い例としては、第1の基材が紙、プ
ラスチック、金属箔などの比較的薄いものであり、第2
の基材が比較的厚い板状のものであるケースが挙げられ
る。Any of the above materials may be used for the first and second base materials, but in most cases, the first base material is a relatively thin material such as paper, plastic, or metal foil. , second
An example of this is a case where the base material is a relatively thick plate.
第1の基材に塗布する熱硬化性樹脂は、例えば、フェノ
ール樹脂、ユリア樹脂、メラミン樹脂、不飽和ポリエス
テル系樹脂、ポリウレタン系樹脂、アミノアルキッド樹
脂、メラミン−エリア共縮合系樹脂、ジアクリルフタレ
ート系樹脂、シリコーン系樹脂などの熱硬化性樹脂、あ
るいは、それらの初期縮合物を主成分とする樹脂液を使
用する。Examples of the thermosetting resin applied to the first base material include phenol resin, urea resin, melamine resin, unsaturated polyester resin, polyurethane resin, amino alkyd resin, melamine-area cocondensation resin, and diacryl phthalate resin. A resin liquid whose main component is a thermosetting resin such as a thermosetting resin, a silicone resin, or an initial condensate thereof is used.
熱硬化性樹脂は必要に応じ、塗布に適した粘度になるよ
う希釈した後、公知のコーティング方法である、例えば
、ロールコート、グラビアコート、バーコード、エアナ
イフコート、フローコート、ディ7ブコート、スプレィ
コートなどの方法により、塗布する。If necessary, the thermosetting resin is diluted to a viscosity suitable for coating, and then coated with a known coating method such as roll coating, gravure coating, barcode coating, air knife coating, flow coating, dip coating, or spray coating. Apply by coating or other methods.
塗布の際には、例えばコーク−付属の乾燥装置を使用し
乾燥させる。この乾燥は、風乾、もしくは若干加熱して
行なうが、加熱の程度は、熱硬化性樹脂を塗布する際の
塗料中に含まれた溶剤を蒸発させれば足りる。加熱の温
度は、コーターにより、また、使用する熱硬化性樹脂の
硬化開始温度にもよるが、25℃〜200℃℃程度であ
り、好ましくは、40℃〜120℃である。At the time of application, it is dried using, for example, a drying device attached to Coke. This drying is performed by air-drying or by slightly heating, but the degree of heating is sufficient to evaporate the solvent contained in the paint when applying the thermosetting resin. The heating temperature is about 25°C to 200°C, preferably 40°C to 120°C, depending on the coater and the curing start temperature of the thermosetting resin used.
このようにして熱硬化性樹脂を塗布した第1の基材の反
対面(非塗布面)側に第2の基材が来るようにして両者
を加熱および加圧してラミネートを行なう。In this way, the second base material is placed on the opposite side (non-coated surface) of the first base material coated with the thermosetting resin, and the two are heated and pressurized to perform lamination.
加熱および加圧は、フラットプレスもしくはロールプレ
スなどの熱プレスで行ない、第2の基材の片面もしくは
両面に、熱硬化性樹脂層を設けた第1の基材を重ねて、
必要に応して最終製品の仕上げ面の艶を調整する意味で
鏡面板、艶消し板、型板などを介して行なう。このとき
接着剤を第1の基材もしくは第2の基材に、または、そ
れらの両方に塗布しておくことができる。Heating and pressurization are performed using a hot press such as a flat press or a roll press, and the first base material provided with the thermosetting resin layer is stacked on one or both sides of the second base material,
This is done using a mirror plate, matte plate, template, etc. to adjust the gloss of the finished surface of the final product as necessary. At this time, the adhesive can be applied to the first base material, the second base material, or both.
接着剤としては、ポリイソブチレンゴム、ポリイソブチ
ルゴム、スチレンブタジェンゴム、ブタジェンアクリロ
ニトリルゴムなどのゴム系樹脂、(メタ)アクリル酸エ
ステル系樹脂、ポリビニルエーテル系樹脂、ポリ酢酸ビ
ニル系樹脂、塩化ビニル−酢酸ビニル共重合体系樹脂、
ポリスチレン系樹脂、ポリエステル系樹脂、ポリアミド
系樹脂、ポリ塩素化オレフィン系樹脂、ポリビニルブチ
ラール系樹脂などの任意の接着性樹脂が使用できる。更
に必要に応じて、硬化剤、充填剤、老化防止剤などの各
種添加剤も添加することができる。Adhesives include rubber resins such as polyisobutylene rubber, polyisobutyl rubber, styrene butadiene rubber, butadiene acrylonitrile rubber, (meth)acrylic acid ester resins, polyvinyl ether resins, polyvinyl acetate resins, and vinyl chloride. -vinyl acetate copolymer resin,
Any adhesive resin such as polystyrene resin, polyester resin, polyamide resin, polychlorinated olefin resin, polyvinyl butyral resin, etc. can be used. Furthermore, various additives such as a curing agent, a filler, and an anti-aging agent can be added as necessary.
この場合、必要であれば、プライマー処理もしくはコロ
ナ処理のような接着性を向上させる前処理を施すことが
できる。In this case, if necessary, pretreatment to improve adhesion such as primer treatment or corona treatment can be performed.
あるいは、ポリ塩化ビニル板とポリ塩化ビニルフィルム
もしくはアクリルフィルムをラミネートするときは接着
剤を用いずに熱溶融によりラミネートすることができる
。Alternatively, when laminating a polyvinyl chloride plate and a polyvinyl chloride film or an acrylic film, the lamination can be carried out by hot melting without using an adhesive.
熱プレスは例えば、80〜200℃程度の温度、20〜
80 Kg7cm”程度の圧力で行ない、熱プレスの時
間としては5〜40分程度である。For example, the heat press is performed at a temperature of about 80 to 200°C, 20 to 200°C.
The hot pressing is carried out at a pressure of about 80 kg and 7 cm, and the hot pressing time is about 5 to 40 minutes.
であるが、140〜180℃の温度、30〜50Kg/
cIIl!の圧力で10〜30分熱プレスし、10〜2
0分程度冷却する方法をとるのが、得られる製品の外観
、物性上好ましい。However, at a temperature of 140-180℃, 30-50Kg/
cIIl! Heat press for 10-30 minutes at a pressure of 10-2
It is preferable to use a method of cooling for about 0 minutes in terms of the appearance and physical properties of the resulting product.
ラミネートの他の方法として、Tダイから押し出した溶
融樹脂を接着剤として用いて、あるいは、これを第1の
基材として用い、押し出し後ロールを用いて行なうこと
ができる。この方法では連続的に、しかも能率よくラミ
ネートを行なうことができる。また、このときも必要に
応じ、第1、第2の基材の接着面を前処理してもよい。Other methods of lamination include using a molten resin extruded from a T-die as an adhesive, or by using this as the first base material and using a roll after extrusion. With this method, lamination can be carried out continuously and efficiently. Also, at this time, the adhesive surfaces of the first and second base materials may be pretreated if necessary.
この発明では、第1の基材に熱硬化性樹脂層を設け、単
に乾燥させたのみの未硬化の状態のものを、第2の基材
とラミネートし、ラミネートの際の熱で硬化を行わせる
ので、熱硬化性樹脂の塗布上の問題がなく、また、第2
の基材として耐熱性の低い物を使用しても、乾燥時に過
大な熱がかからないから、熱変形などの熱による劣化が
起こらない利点がある。In this invention, a thermosetting resin layer is provided on a first base material, and the uncured layer is simply dried and then laminated with a second base material, and cured by heat during lamination. There is no problem in applying the thermosetting resin, and the second
Even if a material with low heat resistance is used as the base material, excessive heat is not applied during drying, so there is an advantage that deterioration due to heat such as thermal deformation does not occur.
以下に、この発明のより具体的な実施例を掲げる。More specific examples of this invention are listed below.
〔実施例1〕
厚み25μmのポリエチレンテレフタレートフィルム(
東しく横裂)を用い、この片面に、完全硬化後に防曇機
能を有する、熱硬化性樹脂(架橋剤としてメラミン樹脂
を配合したポリビニルアルコール樹脂系、第一商工■製
)をグラビアコーティング法により厚み4μmになるよ
う塗布して、100℃の温度で2分間乾燥した。[Example 1] Polyethylene terephthalate film with a thickness of 25 μm (
Using a thermosetting resin (polyvinyl alcohol resin containing melamine resin as a crosslinking agent, manufactured by Daiichi Shoko ■), which has an anti-fog function after complete curing, is coated on one side using the gravure coating method. It was coated to a thickness of 4 μm and dried at a temperature of 100° C. for 2 minutes.
この状態では硬化していないため防曇効果は表れなかっ
た。In this state, the antifogging effect was not exhibited because it was not cured.
次に、上記のフィルムの非コート面に感熱接着剤として
変性ポリエステル樹脂(昭和インク■製)を厚み2μm
になるよう塗布し、乾燥した。Next, a modified polyester resin (manufactured by Showa Ink ■) was applied as a heat-sensitive adhesive to the non-coated surface of the above film to a thickness of 2 μm.
Apply it and let it dry.
上記で得られたものを感熱接着剤層側を下にして、厚み
5mmの無可塑塩化ビニル樹脂板の上に起き、鏡面板を
介してプレスした。このときのプレス条件はプレス熱盤
の表面温度が170℃、圧力30 Kg/cm”であり
、この条件で15分プレスした後、20分間冷却時間を
とり、その後、出来上がった製品を取り出した。The product obtained above was placed on a 5 mm thick non-plastic vinyl chloride resin plate with the heat-sensitive adhesive layer side facing down, and pressed through a mirror plate. The pressing conditions at this time were that the surface temperature of the press hot plate was 170° C. and the pressure was 30 Kg/cm. After pressing under these conditions for 15 minutes, cooling time was taken for 20 minutes, and then the finished product was taken out.
得られた製品は表面の熱硬化製樹脂が硬化しており、防
曇効果が表れた。The thermosetting resin on the surface of the obtained product was cured, and an antifogging effect was exhibited.
なお、ここで防曇効果とは、60℃の湯をビーカーに入
れ、防曇効果を確かめるべき面がこのビーカー側になる
ようにして被検体をかぶせて、60秒間曇りが生じなけ
れば、防45能があると判断するものである。The anti-fog effect here means that if 60°C hot water is poured into a beaker and the test object is placed over the beaker so that the side on which the anti-fog effect is to be checked is facing the beaker, no fogging occurs for 60 seconds. It is judged that the person has 45 abilities.
Claims (2)
層を設け、その反対面側に第2の基材が来るようにして
第1、第2の基材を加熱および加圧することにより、第
1、第2の基材をラミネートすると共に第1の基材の一
方の面上の熱硬化性樹脂の未硬化層を硬化させることを
特徴とする硬化樹脂層を有するラミネート体の製造方法
。(1) An uncured layer of thermosetting resin is provided on one side of the first base material, and the first and second base materials are heated so that the second base material is on the opposite side. and a cured resin layer characterized by laminating the first and second base materials and curing the uncured layer of thermosetting resin on one side of the first base material by applying pressure. A method for manufacturing a laminate body.
ートする特許請求の範囲第1項記載の硬化樹脂層を有す
るラミネート体の製造方法。(2) A method for manufacturing a laminate body having a cured resin layer according to claim 1, wherein the first base material is laminated on both surfaces of the second base material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61311692A JPS63162239A (en) | 1986-12-26 | 1986-12-26 | Manufacture of laminate with cured resin layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61311692A JPS63162239A (en) | 1986-12-26 | 1986-12-26 | Manufacture of laminate with cured resin layer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63162239A true JPS63162239A (en) | 1988-07-05 |
Family
ID=18020316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61311692A Pending JPS63162239A (en) | 1986-12-26 | 1986-12-26 | Manufacture of laminate with cured resin layer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63162239A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0334839A (en) * | 1989-06-30 | 1991-02-14 | Sekisui Chem Co Ltd | Surface treatment of adhered sheet |
US6383328B1 (en) * | 1995-02-07 | 2002-05-07 | Yamaha Corporation | Process for producing decorated article |
-
1986
- 1986-12-26 JP JP61311692A patent/JPS63162239A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0334839A (en) * | 1989-06-30 | 1991-02-14 | Sekisui Chem Co Ltd | Surface treatment of adhered sheet |
US6383328B1 (en) * | 1995-02-07 | 2002-05-07 | Yamaha Corporation | Process for producing decorated article |
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