JPS60115608A - Thermosetting resin composition - Google Patents

Thermosetting resin composition

Info

Publication number
JPS60115608A
JPS60115608A JP22288883A JP22288883A JPS60115608A JP S60115608 A JPS60115608 A JP S60115608A JP 22288883 A JP22288883 A JP 22288883A JP 22288883 A JP22288883 A JP 22288883A JP S60115608 A JPS60115608 A JP S60115608A
Authority
JP
Japan
Prior art keywords
meth
acrylate
parts
thermosetting resin
resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP22288883A
Other languages
Japanese (ja)
Inventor
Keigo Morishita
森下 佳悟
Kimio Yasuda
安田 公男
Yoshiharu Tachibana
橘 喜春
Makoto Nakahara
誠 中原
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanken Kako KK
Original Assignee
Sanken Kako KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sanken Kako KK filed Critical Sanken Kako KK
Priority to JP22288883A priority Critical patent/JPS60115608A/en
Publication of JPS60115608A publication Critical patent/JPS60115608A/en
Pending legal-status Critical Current

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  • Graft Or Block Polymers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

PURPOSE:The titled composition capable of forming a good coating film without inhibition of curing when applied to the surface of resinous wood, prepared by mixing an unsaturated polyester resin or a like resin with a compound having at least three (meth)acryloyl groups. CONSTITUTION:Use is made of a compound having at least three (meth)acryloyl groups in the molecule, such as tri(acryloyl-oxyethyl) isocyanurate, pentaerythitol tetra(meth)acrylate, or dipentaerythritol hexa(meth)acrylate. Namely, 100pts.wt. at least one thermosetting resin selected from the group consisting of unsaturated polyester resisns, epoxyacrylate resins, and allyl resins is mixed with 10- 200pts.wt. above compound. The obtained thermosetting resin composition is dissolved or dispersed in an organic solvent and then mixed with a polymerizable monomer such as styrene, a curing catalyst and other additives to form the composition for painting wood.

Description

【発明の詳細な説明】 て、硬化明害を受けず、而も秀れた塗膜を形成せしめる
熱硬化性樹脂組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a thermosetting resin composition that does not suffer from curing light damage and yet forms an excellent coating film.

従来、ローズウノド、ウA−ルナノト、マホガニーなと
ヤニ分の多い木材においては、不飽件1ポリエステル樹
脂等の熱硬化慴樹脂を塗装する場合硬化111i害か起
こり、美麗な塗膜は?j4られない。そのため塗膜と木
材表面との間にウレクン樹脂のシーラーを塗布するか、
又はメタノール等の溶媒で硬化阻害成分を抽出分離して
から塗装するかなとの対策がとられている。しかし、前
者の場合はウレタン樹脂の塗布、乾燥の手間かはいるた
め煩雑となり、コスト的にも問題である。又、後者の場
合は溶媒で硬化阻害成分を抽出分離する時に硬化阻害成
分たけでなく他の成分も抽出されるため、この種の木材
の特徴である黒っぽい感しかなくなってしまい、商品価
値を著しく低下させてしまう。そへこて、シー□ラー処
理せず又、抽出処理せずに改良する方法の出現か望まれ
ていた。
Conventionally, when painting wood with a high resin content such as rosewood, porcelain, and mahogany with thermosetting resin such as polyester resin, curing 111I damage may occur, resulting in a beautiful coating film. j4 I can't. Therefore, either apply a Urekun resin sealer between the paint film and the wood surface, or
Alternatively, measures have been taken to extract and separate curing-inhibiting components using a solvent such as methanol before painting. However, in the former case, the urethane resin is coated and dried, which is complicated, and also poses a problem in terms of cost. In addition, in the latter case, when the hardening inhibiting components are extracted and separated using a solvent, not only the hardening inhibiting components but also other components are extracted, so the only characteristic of this type of wood is the blackish appearance, which significantly reduces the commercial value. It will lower it. There was a desire for an improved method without using a trowel, sealer treatment, or extraction treatment.

本発明は−1−記問題点を一挙に解決しうる熱硬化性樹
脂組成物に関するものである。即ちa)不飽和ポリエス
テル樹脂、エポキシアクリレート樹脂、アリル樹脂から
選ばれる少なくとも一種の熱硬化性樹脂100重眼部に
対して、b)1分子中に3個以トのアクリロイル基又は
メタクロイル基を含有する化合物を10〜200重M部
をkWすることを特徴とする木材のヤニ止め効果の優れ
た熱硬化性樹脂組成物に関するものである。
The present invention relates to a thermosetting resin composition that can solve the problems listed in -1- all at once. That is, a) at least one type of thermosetting resin selected from unsaturated polyester resins, epoxy acrylate resins, and allyl resins, and b) containing three or more acryloyl groups or methacryloyl groups in one molecule. The present invention relates to a thermosetting resin composition having an excellent tar-preventing effect on wood, characterized in that it contains 10 to 200 parts by weight of a compound containing a kW of a compound.

本発明に使用される不飽和ポリエステル樹脂としては特
に制限されるものでなく、無水フタル酸、イソフタル酸
、テレフタル酸なとの多塩基性飽和酸、無水マレイン酸
、フマル酸、イタコン酸なとの多塩基性不飽和酸、及び
エチレングリコール、プロピレングリコール、ネオペン
チルグリコール、ブタンジオール、2.2−ノ(4′−
ヒドロキシプロポキシフェノール)プロパン、水素化ビ
スフェノールA、トリメチロールプロパンなとの多価ア
ルコールを用いて、脱水縮合したポリエステル樹脂をい
う。
The unsaturated polyester resin used in the present invention is not particularly limited, and includes polybasic saturated acids such as phthalic anhydride, isophthalic acid, and terephthalic acid, maleic anhydride, fumaric acid, and itaconic acid. polybasic unsaturated acids, and ethylene glycol, propylene glycol, neopentyl glycol, butanediol, 2,2-(4'-
It refers to a polyester resin that has been dehydrated and condensed using polyhydric alcohols such as hydroxypropoxyphenol (propane), hydrogenated bisphenol A, and trimethylolpropane.

本発明に使用されるエポキシアクリレート樹脂としては
、エポキシ樹脂と不飽和−塩基酸とを中心に反応させた
もので特に限定されるものではない。エポキシ樹脂とし
ては、ビスフェノール系のエポキシ樹脂、ノボラック型
のエポキシ樹脂等があげられる。又不飽和−塩基酸とし
てはアクリル酸、メタクリル酸等があけられる。不飽和
−塩基酸の一部を二塩基酸、例えばフタル酸、アジピン
酸、フマル酸、コハク酸等に置き換えて使用することも
てきる。
The epoxy acrylate resin used in the present invention is not particularly limited, and is a resin made by reacting an epoxy resin with an unsaturated basic acid. Examples of the epoxy resin include bisphenol-based epoxy resins and novolak-type epoxy resins. Examples of unsaturated basic acids include acrylic acid and methacrylic acid. A portion of the unsaturated basic acids may be replaced with dibasic acids such as phthalic acid, adipic acid, fumaric acid, succinic acid, etc.

本発明に使用されるアリル樹脂は樹脂中にアリル基を含
有しているものを指し、ジアリルフタレート、ジアリル
イソフタレート、ジアリルマレート等のプレポリマーか
例示される。
The allyl resin used in the present invention refers to a resin containing an allyl group, and examples thereof include prepolymers such as diallyl phthalate, diallyl isophthalate, and diallyl maleate.

本発明に使用される1分子中に3個pノ、上のアクリロ
イル基又はメタクロイル基を含イ丁する化合物としては
、トリメチロールプロパントリ(メタ)アクリ1ノート
、ペンタエリスリトールトリ(メタ)アクリレート、ペ
ンタエリスリトールテトラ(メタ)アクリレート、ジペ
ンタエリスリトールテトラ(メタ)アクリレート、ジペ
ンタエリスリトールペンタ(メタ)アクリレート、ジペ
ンタエリスリトールヘキサ(メタ)アクリレート、トリ
ス(メタ)アクリロイルオキシエチルホスフェート、ト
リ((メタ)アクリロイロキシエチル)イソシアヌレー
トなどのアクリル酸、メタクリル酸のエステル類及びト
リアクリルフォルマールなとの多官能モノマーがあげら
れる。これらの合化物のヤニ止め効果の原理は充分に把
握されているわけてはないか、これらの化合物の官能基
の多い稈又融点か高い程好ましい結果を示す。
Compounds containing 3 or more acryloyl or methacryloyl groups in one molecule used in the present invention include trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, Pentaerythritol tetra(meth)acrylate, dipentaerythritol tetra(meth)acrylate, dipentaerythritol penta(meth)acrylate, dipentaerythritol hexa(meth)acrylate, tris(meth)acryloyloxyethyl phosphate, tri((meth)acrylate) Examples include polyfunctional monomers such as esters of acrylic acid and methacrylic acid such as (royloxyethyl) isocyanurate, and triacryl formal. The principle of the tar-preventing effect of these compounds is not fully understood, but the more functional groups the compounds have and the higher the melting point, the better the results.

これら化合物の使用量としては通常、不飽和ポリエステ
ル樹脂、エポキシアクリレート樹脂、アリル樹脂から選
ばれる少なくとも一種の熱硬化性樹脂100@量部に対
して10〜200重量部、好ましくは20〜100重M
部である。10重M部未満の使用量ではヤニ止め効果か
充分でなく、又200重年部を趣えると樹脂のライフか
短かくなるばかりでなく、コストアンプとなる。
The amount of these compounds used is usually 10 to 200 parts by weight, preferably 20 to 100 parts by weight, per 100 parts of at least one thermosetting resin selected from unsaturated polyester resins, epoxy acrylate resins, and allyl resins.
Department. If the amount used is less than 10 parts by weight, the tar-preventing effect will not be sufficient, and if more than 200 parts by weight is used, the life of the resin will not only be shortened, but the cost will be increased.

軒に、これらの組成物はアセトン、メチルエチルケトン
、メチルイソブチルケトン、酢エチ、酸ブチ、ベンゼン
、トルエン、キシレン等の溶媒やスチレン、ジビニルベ
ンゼン、メチルメタクリレート、エチルアクリレート、
エチレングリコールジメタクリレート、ジアリルフタレ
−ト等の重合性単量体を混合して使用されることか多い
In general, these compositions contain solvents such as acetone, methyl ethyl ketone, methyl isobutyl ketone, ethyl acetate, butyl acid, benzene, toluene, xylene, styrene, divinylbenzene, methyl methacrylate, ethyl acrylate,
It is often used in combination with polymerizable monomers such as ethylene glycol dimethacrylate and diallyl phthalate.

更に目的に応じて、揺変剤、耐摩耗向上剤、着色剤、ゲ
ル化防1F剤、無機充填剤等を添加することかできる。
Furthermore, depending on the purpose, a thixotropic agent, an abrasion resistance improver, a coloring agent, an anti-gelling agent, an inorganic filler, etc. may be added.

この熱硬化性樹脂組成物を木材に加工する方法としては
ベンゾイルパーオキサイド、ターシャリ−ブチルパーベ
ンゾエート、ジクミルパーオキサイド、ラワロイルパー
オキサイド等の重合開始剤を用いる加熱硬化の方法、メ
チルエチルケントパーオキサイド、メチルイソブチルケ
ントバー オ+サイド等の硬化剤とナフテン酸コバルト
等の硬化促進剤とを併用する常7!ll!硬化の方法、
ベンゾイン、ベンジル、ベンゾインエーテル等の光増感
剤を使用する光硬化の方法及び電子線硬化の方法かある
Methods for processing this thermosetting resin composition into wood include heat curing using a polymerization initiator such as benzoyl peroxide, tert-butyl perbenzoate, dicumyl peroxide, and rawaloyl peroxide; Always use a curing agent such as oxide, methyl isobutyl chloride + side, etc. together with a curing accelerator such as cobalt naphthenate! ll! method of curing,
There are photocuring methods using photosensitizers such as benzoin, benzyl, benzoin ether, etc., and electron beam curing methods.

使用される木材としてはインドローズ、アンデスローズ
、パープルローズ、アメリカンウオールナツト、マホガ
ニー、チーク、コクタン、カブール等の重合μ■害醪分
であるヤニ分の多い樹種が対象となる。これらの木材は
通常その木材の薄単板を合板等に貼り合せたツキ板とし
て用いられることが、最近多くなっている。
The wood species used include Indian rose, Andean rose, purple rose, American walnut, mahogany, teak, ebony, and Kabul, which have a high resin content, which is a harmful substance. Recently, these woods have been increasingly used as veneer boards, which are usually made by laminating thin veneers of these woods to plywood or the like.

木材に塗装する方法としては直接木材にロールコータ−
等で塗布する方法、一旦フイルムに塗装し、それを木材
表面に転写する方法、スプレーアンプで吹きつける方法
等があり、最後にEl−上げをよくするために加熱プレ
スする事が多い。通常膜厚は50〜1000ミクロン好
ましくは100〜500ミクロンである。
The method for painting wood is to use a roll coater directly on the wood.
There are several methods, such as coating it on a film and then transferring it to the wood surface, and spraying it with a spray amplifier.Finally, heat pressing is often used to improve the El-raising. The film thickness is usually 50 to 1000 microns, preferably 100 to 500 microns.

以下実施例により本発明を具(1的に説明するか、本発
明はそれらに限定されるものではない尚実施例、比較例
における部及び%は特に記載のない限り、すへて重惜部
及び瑣事%を表わす。
The present invention will be explained below with reference to Examples (although the present invention is not limited thereto), parts and percentages in Examples and Comparative Examples are given with no hesitation unless otherwise specified. and represents a trivial %.

実施例 1 イソフタル酸04モル、無水マレイン酸06モル、ネオ
ペンチルグリコール0.3モル、フロピレンゲリコール
075モルを脱水縮合して、酸価12の不飽和ポリエス
テル樹脂を得た。この樹脂100部に対して、ペンタエ
リスリトールテトラアクリレート60部、アセトン10
0部、トルエン60部、ベンゾイルパーオキサイド3部
を加えて、樹脂組成物となし、これをポリエステルフィ
ルム上に塗布し、80℃で乾燥し膜+9: 200μの
塗膜を得た。これをアンデスローズ1.lt板を貼り合
せた板の表面に塗膜か板と接するように置き、120℃
、10に97−で15分間プレスした。
Example 1 04 moles of isophthalic acid, 06 moles of maleic anhydride, 0.3 moles of neopentyl glycol, and 075 moles of furopylene gellicol were subjected to dehydration condensation to obtain an unsaturated polyester resin having an acid value of 12. For 100 parts of this resin, 60 parts of pentaerythritol tetraacrylate, 10 parts of acetone.
0 parts of toluene, 60 parts of toluene, and 3 parts of benzoyl peroxide were added to prepare a resin composition, which was coated on a polyester film and dried at 80°C to obtain a coating film with a thickness of +9: 200μ. Add this to Andes Rose 1. Place the LT board on the surface of the board so that it is in contact with the paint film or the board, and heat at 120°C.
, 10 and 97- for 15 minutes.

街られたプレス品の表面には硬化阻害に基つく白い斑点
は見られず、光沢も優れていた。
No white spots due to curing inhibition were observed on the surface of the pressed product, and the gloss was excellent.

:1′ I11+) 例 2 スミエポキシF、 S A −011(エポキシ当用4
70、住友化学丁業社品)04モルとメタクリル酸08
モルとを付加反応して、酸価2のエポキシアクリレート
樹脂を得た。この樹脂j。
:1' I11+) Example 2 Sumiepoxy F, S A-011 (Epoxy purpose 4
70, Sumitomo Chemical Co., Ltd. product) 04 mol and methacrylic acid 08
An epoxy acrylate resin having an acid value of 2 was obtained by addition reaction with molar. This resin j.

0部に対してンペンタエリスリト−ルヘキサメタクリレ
ート20部、エチレングリコールジメタクリレート10
0部、ベンゾインメチルエーテル10部を加えて樹脂組
成物とした。これをインドローズ単板を貼り合せたツキ
板の表向に塗装しその表面にポリエステルフィルムを置
いて紫外線照射装置で5分照射して硬化せしめた。
0 parts, 20 parts of empentaerythritol hexamethacrylate, 10 parts of ethylene glycol dimethacrylate
0 parts and 10 parts of benzoin methyl ether were added to prepare a resin composition. This was applied to the surface of a veneer board to which Indian rose veneers were bonded, a polyester film was placed on the surface, and the film was irradiated with ultraviolet rays for 5 minutes to cure it.

表面は白い斑点は見られず、光沢も良好てあったっ実施
例 3 ジアリルフタレート樹脂(グイソーダノブA、大阪曹達
玉業社品)100部に対して、トリ(メタアクリロイロ
キシエチル)インシアヌレ−)100部、アセトン12
0部、ベンゼン80部、ベンゾイルパーオキサイド3部
を11■えて樹脂組成物となし、これをチーク単板を貼
り合せたツキ板の表面に塗布し、80℃で乾燥し、+1
.J厚3 n +1μの塗膜を得た。この上にポリエス
テルフィルムを置き140℃、10にり/4で10分間
プレスした。
No white spots were observed on the surface, and the gloss was good.Example 3: 100 parts of diallyl phthalate resin (Guisoda Nobu A, Osaka Soda Gyokugyo Co., Ltd.) was mixed with 100 parts of tri(methacryloyloxyethyl) incyanure). part, acetone 12
0 parts, 80 parts of benzene, and 3 parts of benzoyl peroxide were mixed in 11 parts to make a resin composition. This was applied to the surface of a veneer board with teak veneer laminated, dried at 80°C, and +1
.. A coating film with a thickness of 3 n + 1 μm was obtained. A polyester film was placed on top of this and pressed at 140° C. and 10/4 for 10 minutes.

得られたプレス品の表面は白い斑点もなく光沢も良好で
あった。
The surface of the obtained pressed product had no white spots and had good gloss.

実施例 4 実Ifli例1と同様の不飽和ポリエステル樹脂100
部に対[7てジペンタエリスリトールペンタアクリレー
ト30部、スチレン110部、揺変剤(酸化珪素)2部
、ナフテン酸コバルト1部、メチルエチルケントパーオ
キサイド3部を加えて樹脂組成物とした。これをマホカ
二−ノ単板を貼り合せたツキ板の表面にスプレー法で塗
装し、その上にポリエステルフィルム置きローラーで均
一な塗膜となし、宇高て4時間放置して硬化せしめた。
Example 4 Unsaturated polyester resin 100 similar to actual Ifli example 1
30 parts of dipentaerythritol pentaacrylate, 110 parts of styrene, 2 parts of thixotropic agent (silicon oxide), 1 part of cobalt naphthenate, and 3 parts of methyl ethyl kent peroxide were added to [7] to prepare a resin composition. This was applied by spraying onto the surface of a veneer board to which Mahocanino veneer was bonded, and a polyester film was placed on top of it with a roller to form a uniform coating, which was then left at Utaka for 4 hours to harden.

得られた硬化塗膜には白い斑点は児られす光沢も良好で
あった。
The resulting cured coating had no white spots and had good gloss.

比較例 1 イソフタル酸04モル、無水マレイン酸06モル、ネオ
ペンチルグリコール03モル、プロピレングリコール0
75モルを脱水縮合して、酸価12の6飽和ポリエステ
ル樹脂を得た。この樹脂100部に対してジアリルフタ
レートモノマー20部、アセトン70部、トルエン50
M≦、ヘンソイルパーオキサイド2部を加えて樹脂組成
物をつくった。この樹脂液をポリエステルフィルム1−
に塗布し80℃て乾燥して、そRをアンデスローズ単板
を貼り合せたツキ板の表面に塗膜か板と接するように置
き120°C10に9 / cAて15分間プレスした
Comparative Example 1 Isophthalic acid 04 mol, maleic anhydride 06 mol, neopentyl glycol 03 mol, propylene glycol 0
75 moles were subjected to dehydration condensation to obtain a 6-saturated polyester resin with an acid value of 12. For 100 parts of this resin, 20 parts of diallyl phthalate monomer, 70 parts of acetone, 50 parts of toluene
M≦, a resin composition was prepared by adding 2 parts of Hensoil peroxide. This resin liquid was applied to the polyester film 1-
After drying at 80°C, SoR was placed on the surface of a veneer board to which Andes Rose veneer was bonded so that the coating film was in contact with the board, and pressed at 120°C, 10°C, and 9/cA for 15 minutes.

得られたプレス品の表面には硬化[l害のヤニ分に基つ
く白い斑点か各所に見られた。jl’; i< f’l
は全熱劣っていた。
On the surface of the obtained pressed product, white spots due to hardened tar were seen in various places. jl';i<f'l
The overall fever was inferior.

比較例 2 比較例1のジアリルフタレートモノマー20部の代りに
ペンタエリスリト ルナトラアクリレート5部を用いる
点ld外は比較例1と(11様の方法でプレス品を得た
。プレス品の表向の白い斑点は比較例1よりは少なかっ
たか、少し見られ実用上問題かあった。又光沢性も充分
てなかった。
Comparative Example 2 A pressed product was obtained in the same manner as Comparative Example 1 and (11) except that 5 parts of pentaerythritolunatraacrylate was used instead of 20 parts of diallyl phthalate monomer in Comparative Example 1. The white spots were fewer or slightly visible than in Comparative Example 1, posing a practical problem.Also, the gloss was not sufficient.

Claims (1)

【特許請求の範囲】 1、a)不飽和ポリエステル樹脂、エポキシアクリレー
ト樹脂、アリル樹脂から選はれる少なくとも一種の熱硬
化性樹脂100重111部に対して1))1分子中に3
個以上のアクリロイル基又はメタクロイル基を含有する
化合物を10〜200 @帽部を含有することを特徴と
する木材のヤニ市め効果の優れた熱(i1j化↑11樹
脂糾成物。 21分子中に3個以」二のアクリロイル基又はメタクロ
イル基を含有する化合物かトリ((メタ)アクリロイロ
キシエチル)インシアヌレートである特許請求の範囲第
1伯記載の熱硬化性樹脂組成物。 31分子中に3個リドのアクリロイル基又はメタクロイ
ル基を含有する化合物かペンタエリスリトールテトラ(
メrり)アクリレートである特許請求の範囲第1項記4
曳の熱硬化性樹脂組成物。 41分子中に3個以」二のアクリロイル基又はメタクロ
イル基を含有する化合物かジペンタエリスリトールテト
ラ(メタ)アクリレート、ジペンタエリスリトールペン
タ(メタ)アクリレート、ジペンタエリスリトールヘキ
サ(−メタ)アクリレートから選はれる少なくとも一種
である特許請求の範囲第1項記載の熱1i!II化性樹
脂糾成物。
[Claims] 1. a) At least one thermosetting resin selected from unsaturated polyester resins, epoxy acrylate resins, and allyl resins, based on 100 parts by weight and 111 parts: 1)) 3 per molecule
10 to 200 compounds containing acryloyl groups or methacryloyl groups or more in the cap part. The thermosetting resin composition according to claim 1, which is a compound containing three or more acryloyl or methacryloyl groups or tri((meth)acryloyloxyethyl)in cyanurate. 31 molecules Compounds containing three acryloyl or methacryloyl groups or pentaerythritol tetra (
Claim 1, item 4, which is acrylate
Hiki's thermosetting resin composition. 41 Compounds containing 3 or more acryloyl or methacryloyl groups in the molecule, selected from dipentaerythritol tetra(meth)acrylate, dipentaerythritol penta(meth)acrylate, dipentaerythritol hexa(-meth)acrylate The heat 1i! according to claim 1, which is at least one type of heat 1i! II-formable resin compact.
JP22288883A 1983-11-25 1983-11-25 Thermosetting resin composition Pending JPS60115608A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22288883A JPS60115608A (en) 1983-11-25 1983-11-25 Thermosetting resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22288883A JPS60115608A (en) 1983-11-25 1983-11-25 Thermosetting resin composition

Publications (1)

Publication Number Publication Date
JPS60115608A true JPS60115608A (en) 1985-06-22

Family

ID=16789442

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22288883A Pending JPS60115608A (en) 1983-11-25 1983-11-25 Thermosetting resin composition

Country Status (1)

Country Link
JP (1) JPS60115608A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61126179A (en) * 1984-11-22 1986-06-13 Toyo Ink Mfg Co Ltd Electron beam curing coating composition
JPS62149714A (en) * 1985-12-25 1987-07-03 Osaka Soda Co Ltd Resin composition for laminated sheet
JPS62156114A (en) * 1985-12-27 1987-07-11 Osaka Soda Co Ltd Resin composition for laminated sheet
JPS6327554A (en) * 1986-07-22 1988-02-05 Dainippon Ink & Chem Inc Molding material for frp
JPS63150346A (en) * 1986-12-12 1988-06-23 Osaka Soda Co Ltd Resin composition for laminated sheet
JPS63205348A (en) * 1987-02-23 1988-08-24 Dainippon Ink & Chem Inc Nonwaxy unsaturated polyester resin composition for paint
JPS644605A (en) * 1987-06-27 1989-01-09 Daiso Co Ltd Thermosetting molding material
JPS6490210A (en) * 1987-10-01 1989-04-06 Kayaku Noury Corp Hard coating composition and its cure

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61126179A (en) * 1984-11-22 1986-06-13 Toyo Ink Mfg Co Ltd Electron beam curing coating composition
JPH0510395B2 (en) * 1984-11-22 1993-02-09 Toyo Ink Mfg Co
JPS62149714A (en) * 1985-12-25 1987-07-03 Osaka Soda Co Ltd Resin composition for laminated sheet
JPS62156114A (en) * 1985-12-27 1987-07-11 Osaka Soda Co Ltd Resin composition for laminated sheet
JPS6327554A (en) * 1986-07-22 1988-02-05 Dainippon Ink & Chem Inc Molding material for frp
JPS63150346A (en) * 1986-12-12 1988-06-23 Osaka Soda Co Ltd Resin composition for laminated sheet
JPH0511551B2 (en) * 1986-12-12 1993-02-15 Daisow Co Ltd
JPS63205348A (en) * 1987-02-23 1988-08-24 Dainippon Ink & Chem Inc Nonwaxy unsaturated polyester resin composition for paint
JPS644605A (en) * 1987-06-27 1989-01-09 Daiso Co Ltd Thermosetting molding material
JPS6490210A (en) * 1987-10-01 1989-04-06 Kayaku Noury Corp Hard coating composition and its cure

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