JPS60183127A - Heat-fusing painting - Google Patents

Heat-fusing painting

Info

Publication number
JPS60183127A
JPS60183127A JP3862384A JP3862384A JPS60183127A JP S60183127 A JPS60183127 A JP S60183127A JP 3862384 A JP3862384 A JP 3862384A JP 3862384 A JP3862384 A JP 3862384A JP S60183127 A JPS60183127 A JP S60183127A
Authority
JP
Japan
Prior art keywords
resin
coating
film
coated
heat
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
JP3862384A
Other languages
Japanese (ja)
Inventor
Toshio Kobayashi
俊夫 小林
Hiroo Muramoto
博雄 村本
Tomoaki Kawagishi
川岸 外茂明
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.)
Nippon Soda Co Ltd
Original Assignee
Nippon Soda Co Ltd
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 Nippon Soda Co Ltd filed Critical Nippon Soda Co Ltd
Priority to JP3862384A priority Critical patent/JPS60183127A/en
Publication of JPS60183127A publication Critical patent/JPS60183127A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To prevent a toxicity and an air pollution caused from diffusion of solvents by applying and fixing, with heat and pressure, a resin layer surface of a resin film which is coated upon either one side or both sides of a substrate strip over a surface of an object to be painted. CONSTITUTION:A coated resin film which has been obtained by application of resin on either one or both sides of a substrate strip is used, and by applying and fixing, with heat and pressure, the surface of resin layer of the coated resin film over the surface of an object to be painted a painting film layer which contains a coated resin is formed. As for coating resin to be used on a substrate strip, urea resin, polyethylene resin, polystyrene resin etc. are quoted. Heat and pressure adhesion between the coated resin film and the object to the painted can be easily performed by using various types of heat press, heat press rolls and the like.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は、熱融着塗装法に関する。さらに詳しくは、フ
ィルム状支持体に樹脂を塗布して得られるコーティング
樹脂フィルムの樹脂層面を被塗物の表面にあてて熱圧着
により、コーティング樹脂を被塗面上に融着せしめてフ
ィルム状支持体を含む塗膜層を形成する塗装法に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a thermal fusion coating method. More specifically, the resin layer side of a coating resin film obtained by applying a resin to a film-like support is applied to the surface of the object to be coated, and the coating resin is fused onto the surface to be coated by thermocompression bonding. The present invention relates to a coating method for forming a coating layer including a body.

〔発明の従来技術とその問題点) 従来、使用されている表面の保護、美観、標示等を目的
とした枦装方法としては、液状型塗装法では刷毛m”)
、エアースプレー、エアレススプレー、ロールコータ−
、フローコーター、静ite装、電着塗装等が挙げられ
、また粉体型塗装では被塗物の加熱による流動浸漬、静
電塗装後の溶融塗装等罠よって行われ1いるが、これら
の塗装方法においては多くの問題点が残されている。例
えば、溶剤型塗料を用いた場合、塗料中に含まれる有機
溶剤のために人体への悪影響や大気汚染が懸念され、ま
た乾燥硬化工程に長時間を要し、さらに塗膜も溶剤の揮
発に伴って収縮、肉やせが起り、このため表面多孔質の
被塗物等には数回の重ね塗り工程を要し生産性が著しく
悪い等の問題があった。
[Prior art of the invention and its problems] Conventionally used methods of covering surfaces for the purpose of surface protection, aesthetics, marking, etc. include liquid coating methods such as brush m'')
, air spray, airless spray, roll coater
, flow coater, static coating, electrodeposition coating, etc., and in powder type coating, there are methods such as fluid immersion by heating the object to be coated, melt coating after electrostatic coating, etc.1, but these coatings Many problems remain with the method. For example, when using solvent-based paints, there are concerns about negative effects on the human body and air pollution due to the organic solvents contained in the paints, the drying and curing process takes a long time, and the paint film is also affected by the volatilization of the solvent. As a result, shrinkage and thinning of the coating material occur, which causes problems such as the need for several recoating steps for objects with porous surfaces, resulting in extremely poor productivity.

一方、無溶剤型塗料を用いた場合、溶剤型塗料に比べて
高粘度用塗装機例えば、エアレススプレー、フローコー
ター、p−ルコーターなどカ必要であり、また粉体型塗
料においては流動浸漬塗装機等の大型設備と高エネルギ
ーが必要で木材、プラスチック等の加温時に変形し易い
被塗物への塗装は困難であると言う問題があった。
On the other hand, when using solvent-free paints, a high viscosity coating machine such as an airless sprayer, flow coater, or p-lu coater is required compared to solvent-based paints, and fluid-dip coating machines are required for powder-type paints. This method requires large equipment and high energy, making it difficult to coat materials that easily deform when heated, such as wood and plastic.

これらの問題点を解決する方法として、近年電子線、γ
線、紫外線照射等による放射線、光硬化型塗料が開発さ
れているが、膨大な設備投資、装置の大型化が必要であ
り、一般的に容易に使用するには問題がある。また、前
述の塗装法の他K。
In recent years, electron beams, γ
Radiation-curable coatings, such as UV rays, and photocurable coatings, have been developed, but they require a huge amount of equipment investment and large-sized equipment, and there are problems in general ease of use. In addition to the above-mentioned painting method, K.

熱硬化性樹脂板を接着する方法も用いられ1いるが、塗
装材料自体の持っている本来の感触、材質感の表現は、
列置塗装仕上げされたものにおよばない。
A method of gluing thermosetting resin plates is also used1, but the original feel and texture of the coating material itself cannot be expressed.
It is not as good as the one that has been painted in a row.

以上のように現在用いられている塗装方装および被塗物
の表面に硬化樹脂板を接着する表面保護と美観の表現方
法には、各々種々の問題が内在している。
As described above, there are various problems inherent in the currently used painting methods and surface protection and aesthetic expression methods of adhering a cured resin plate to the surface of the object to be coated.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

本発明は、前述した従来の塗装法の問題点を解消したも
ので溶剤、揮散による毒性や大気汚染問題がなく、また
特殊な塗装装置を要すことなしに塗装工程に要する時間
を大巾に短縮せしめ、しかも強x兎で仕上り性良好な塗
膜層を形成せしめる塗装方法を提供することにある。
The present invention solves the above-mentioned problems of the conventional painting method, eliminates the toxicity and air pollution problems caused by solvents and volatilization, and greatly reduces the time required for the painting process without requiring special painting equipment. It is an object of the present invention to provide a coating method capable of forming a coating layer that is short, strong, and has a good finish.

〔発明の概要〕[Summary of the invention]

本発明者らは、前述した問題点に留意しなから′鋭意検
討を重ねた結果、予じめフィルム状支持体の片面または
両面に樹脂を塗布して得られたコーティング樹脂フィル
ムを用い、該コーティング樹脂フィルムの樹脂層面を被
塗物の表面にあてχ熱圧着することKより、コーティン
グ樹脂を被塗面上に融着せしめてフィルム状支持体を含
む塗膜層を形成する熱融着塗装法を採用することにより
、本発明の所期の目的を達成しうろことを見い出し、本
発明を完成するに至った。
The inventors of the present invention have conducted intensive studies while keeping the above-mentioned problems in mind, and as a result, the present inventors have discovered that a coated resin film obtained by coating a resin on one or both sides of a film-like support in advance is used. Heat-fusion coating in which the resin layer side of the coating resin film is applied to the surface of the object to be coated and subjected to thermal compression bonding to fuse the coating resin onto the surface to be coated to form a coating layer containing a film-like support. By employing this method, the inventors discovered that the intended purpose of the present invention could be achieved and completed the present invention.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明においてフィルム状支持体に塗布する樹脂は、通
常塗料用として用いられる樹脂類および硬化剤、促進剤
、溶剤、顔料、染料、安定剤、増感剤、各種充填剤等を
配合した樹脂組成物が使用され、これらは通常の塗工法
、例えばバーコーター、ナイフコーター、ロールコータ
−、フローコーター、浸漬性等圧より均一に所定のフィ
ルム状支持体上にコーティングせしめた後、該樹脂組成
物中に含まれる揮発分を乾燥除去し、または必要に応じ
、半硬化あるいは完全に硬化せしめてコーティング樹脂
フィルムが作成される。
In the present invention, the resin applied to the film support is a resin composition containing resins commonly used for coatings, curing agents, accelerators, solvents, pigments, dyes, stabilizers, sensitizers, various fillers, etc. These resin compositions are coated uniformly on a predetermined film-like support using a conventional coating method such as a bar coater, knife coater, roll coater, flow coater, immersion isostatic pressure, etc. A coating resin film is prepared by drying and removing the volatile components contained therein, or by semi-curing or completely curing as required.

上記のフィルム状支持体への樹脂コーティングは、通常
膜厚が100μm以下であれば1〜2回コーティングで
良いが、厚い塗膜層を必要とする場合は、塗布乾燥を数
回繰り返すか、または塗布後加熱などにより半硬化ある
いは完全に樹脂層を硬化せしめた後、再び前述の塗工法
によりコーティングを行い所定の膜厚を有する複合樹脂
層よりなる熱融着用コーティング樹脂フィルムを作成す
ることができる。
The above resin coating on the film-like support usually requires coating once or twice if the film thickness is 100 μm or less, but if a thick coating layer is required, coating and drying may be repeated several times or After coating, the resin layer is semi-cured or completely cured by heating, etc., and then coated again by the above-mentioned coating method to create a heat-sealing coating resin film consisting of a composite resin layer having a predetermined thickness. .

上記方法によって作成されたコーティング樹脂−フィル
ムは、該コーティング樹脂フィルムの樹脂層面を塗装目
的とする被塗物の表面にあてて熱圧着を行うが、この熱
圧着は一般に使用されている各種熱プレス、熱プレスロ
ール等を用い又容易代行5ことができ、熱圧着条件は用
いるコーティング樹脂フィルム、被塗物等によって異な
るが、通常、圧着圧力1〜30KP/I!!、圧着温度
・時間 60〜b 圧着をすることにより、コーティング樹脂な被塗面に融
着せしめ、フィルム状支持体を含む塗膜層を形成させる
The coating resin film produced by the above method is thermocompressed by applying the resin layer surface of the coating resin film to the surface of the object to be coated. , can be easily carried out using a hot press roll, etc., and the thermocompression bonding conditions vary depending on the coating resin film used, the object to be coated, etc., but usually the compression pressure is 1 to 30 KP/I! ! , Pressure bonding temperature/time 60-b By press-bonding, the coating resin is fused to the surface to be coated to form a coating layer including a film-like support.

本発明におけるフィルム状支持体としては、紙、剥離紙
のような加工紙、化学繊維、熱可塑性樹脂フィルム等で
樹脂が均一にコーティング可能なものであれば、特にこ
れらに限定されるものではな%S。
The film-like support used in the present invention is not particularly limited to paper, processed paper such as release paper, chemical fiber, thermoplastic resin film, etc., as long as it can be uniformly coated with resin. %S.

フィルム状支持体は製造略画および取扱い作業性、熱伝
導性を考慮した場合、出来るだけ薄いものが好ましい。
It is preferable that the film-like support be as thin as possible in consideration of manufacturing scheme, handling efficiency, and thermal conductivity.

また該フィルム状支持体が熱融着塗装後、塗膜層中に残
留して塗膜層の一部となり、靭 形成される塗膜層をより強らなものにする。また、塗装
目的によって透明な塗膜層を必要とする場合は、紙、繊
維等のフィルム状支持体は中の空隙を完全に樹脂で充填
し、かつ樹脂とフィルム状支持体は互に屈折率の近いも
のを選択して用いられる。
Further, the film-like support remains in the coating layer after heat-fusion coating and becomes a part of the coating layer, thereby making the coating layer tougher. In addition, if a transparent coating layer is required depending on the purpose of painting, the voids in the film support such as paper or fibers should be completely filled with resin, and the refractive index of the resin and film support should be The closest one is selected and used.

なお、用途によっては、フィルム状支持体に着色、模様
付け、エンボス加工したものを用いて被塗装面の着色、
模様付け、変り塗り等に応用することも可能である。
Depending on the application, colored, patterned, or embossed film supports may be used to color the surface to be painted.
It can also be applied to patterning, different painting, etc.

本発明における前述のフィルム状支持体への塗布樹脂と
しては、通常の塗料用樹脂類、例えばフェノール樹脂、
尿素樹脂、エポキシ樹脂、アルキッド樹脂、メラミン樹
脂、ポリウレタン樹脂、不飽和ポリエステル樹脂、ブチ
ラール樹脂、ポバール樹脂、アクリル樹脂、塩化ゴム樹
脂、塩化ビニル樹脂、酢酸ビニル樹脂、ポリエチレン樹
i旨、ポリプロピレン樹脂、ポリブタジェン系樹脂、ポ
リスチレン系樹脂、塩化ビニル−酢酸ビニル共重合体樹
脂、アクリル共重合体樹脂、ポリプタジエ/共重合体樹
脂、硝化綿樹脂、石油樹脂、ケトン樹脂等の熱硬化性ま
たは熱可塑性樹脂が挙げられる。
In the present invention, the resin to be applied to the film-like support mentioned above may be a common resin for coating, such as a phenol resin,
Urea resin, epoxy resin, alkyd resin, melamine resin, polyurethane resin, unsaturated polyester resin, butyral resin, poval resin, acrylic resin, chlorinated rubber resin, vinyl chloride resin, vinyl acetate resin, polyethylene resin, polypropylene resin, polybutadiene Examples include thermosetting or thermoplastic resins such as polystyrene resins, vinyl chloride-vinyl acetate copolymer resins, acrylic copolymer resins, polyptadiene/copolymer resins, nitrified cotton resins, petroleum resins, and ketone resins. It will be done.

これらの塗料用樹脂は単独または2種以上の混合系で用
いられる。
These coating resins may be used alone or in a mixture of two or more.

なお、熱硬化性樹脂を用いる場合、併用される硬化剤と
しては、ラジカル重合開始剤としてジアシルパーオキサ
イド、ジアルキルパーオキサイド、“パーオキシエステ
ル、ハイドロパーオキサイド、ケトンパーオキサイド、
パーオキシケタール等の有機過酸化物類およびこれらの
促進剤としてジメチルアニリン等のアミン化合物、ナフ
テン酸コバルトなどのカルボン酸金属塩類が挙げられ、
またエポキシ樹脂硬化剤として、ジエチレントリアミン
などのアミン類、無水フタル酸等のカルボン酸無水物類
、BF、系化合物、分子内に一8H基、−NCO基、−
C0NH基のいずれかを1個以上有する化合物およびこ
れらの促進剤として2−エチルイミダゾール、ベンジル
ジメチルアミン、臭化テトラエチルアンモニウム、塩化
コリン、苛性カリ等の公知のものが用いられる。
In addition, when using a thermosetting resin, curing agents used in combination include diacyl peroxide, dialkyl peroxide, "peroxy ester, hydroperoxide, ketone peroxide," as a radical polymerization initiator.
Organic peroxides such as peroxyketal and their promoters include amine compounds such as dimethylaniline, carboxylic acid metal salts such as cobalt naphthenate,
In addition, as an epoxy resin curing agent, amines such as diethylene triamine, carboxylic acid anhydrides such as phthalic anhydride, BF, type compounds, 18H group, -NCO group, -
Known compounds such as 2-ethylimidazole, benzyldimethylamine, tetraethylammonium bromide, choline chloride, and caustic potash are used as compounds having one or more of C0NH groups and promoters thereof.

また、必要に応じてトリメチロールプ四パントリメタク
リレート、エチレングリコールジメタクリレート、ジビ
ニルベンゼン、トリアリルイソシアヌレート等のビニル
モノ1−類、フェノール樹脂、尿素樹脂、メラミン樹脂
等を配合することも可能である。
Furthermore, it is also possible to blend vinyl mono-1-s such as trimethylol tetrapane trimethacrylate, ethylene glycol dimethacrylate, divinylbenzene, and triallyl isocyanurate, phenol resin, urea resin, melamine resin, etc., if necessary. .

本発明で用いる塗料用樹脂に安定剤としての酸化防止剤
、紫外線吸収剤等を添加しても良く、酸化防止剤として
、例えばハイドロキノン、芳香族アミン、アルデヒドア
ミン縮金物、フェニル−β−ナフチルアミン; 紫外線吸収剤として、例えばサリチル酸ニスチル系、ヒ
ドロギシペンゾフヱノン系、ベンゾトリアゾール系等が
挙げられ、これらの安定剤の添加tvt、一般的KO,
01〜5重量%である。
Antioxidants, ultraviolet absorbers, etc. as stabilizers may be added to the coating resin used in the present invention, and examples of antioxidants include hydroquinone, aromatic amines, aldehyde amine condensates, phenyl-β-naphthylamine; Examples of ultraviolet absorbers include nistyl salicylate type, hydroxypenzophenone type, benzotriazole type, etc. Addition of these stabilizers tvt, general KO,
01 to 5% by weight.

また、塗料添加剤として用いられる塗膜着色剤としては
、有機顔料、カーボンブラック、無機顔料、染料、金属
粉末等、また必要に応じて前記着色剤の浮き防止剤、色
別れ防止剤、レシチン、ナフテン酸金属塩、脂肪酸、界
面活性剤等が副添加剤として用いられる。
In addition, coating film colorants used as paint additives include organic pigments, carbon black, inorganic pigments, dyes, metal powders, etc., and if necessary, anti-lifting agents, color separation prevention agents, lecithin, etc. Naphthenic acid metal salts, fatty acids, surfactants, etc. are used as sub-additives.

なお、上記塗料添加剤の他に熱圧着時のガスチェツキン
グ剤、酸化型ドライヤー等も用いられる。
In addition to the above paint additives, gas checking agents during thermocompression bonding, oxidation dryers, etc. may also be used.

本発明において用いられる被塗物は前述の如く、金属、
プラスチック、無機材質、木材等の表面塗装とし℃用い
られ、プラスチック、無機材質等の塗膜密着性の低い被
塗物に対しては、予め密着性を付与せしめるプライマー
塗装を本発明による熱融着塗装または一般塗装方法によ
って行った後、熱融着塗装を行うことKよって被塗物と
の密着性の高い塗膜が得られる。また、より高級な塗面
仕上げを要求する場合は、本発明によりて熱融着塗装さ
れ、形成された塗膜層の表面を研磨した後、である。
As mentioned above, the objects to be coated used in the present invention include metals,
It is used for surface coating of plastics, inorganic materials, wood, etc., and for coated objects with low coating film adhesion such as plastics and inorganic materials, the heat fusion method of the present invention is used to apply a primer coating that gives adhesion in advance. A coating film with high adhesion to the object to be coated can be obtained by applying heat fusion coating after coating or a general coating method. Further, if a higher quality coating surface finish is required, the surface of the coating layer formed by heat-fusion coating according to the present invention should be polished.

〔発明の効果〕〔Effect of the invention〕

本発明の熱融着塗装法は、有機溶剤による公害良好な塗
膜層を形成することができる。
The thermal fusion coating method of the present invention can form a coating layer that is free from pollution caused by organic solvents.

〔発明の実施例〕[Embodiments of the invention]

本発明の詳細を実施例により具体的に説明するが、本発
明はその要旨を越えない限り、何らこれらの実施例によ
り制約されるものでない。なお、試料調整、実施例中の
部および%は重量部および重量%を示す。
The details of the present invention will be specifically explained by examples, but the present invention is not limited to these examples in any way unless the gist thereof is exceeded. Note that parts and % in sample preparation and examples indicate parts by weight and % by weight.

(A)試料調整 試料1 撹拌機、滴下ロート、温度針、環流冷却管、乾燥空気吹
き込み管を付した四ツロ丸底フラスコに平均分子量1,
000、重合体鎖のプタジ≦−位・092%が1.2−
結合からなるポリブタジェンジオールを原料とした遊離
インシアネート3.6%を有するウレタン変性誘導体(
日本曹達社製Nl5SO−PBTL−1,000、酢酸
エチル50%品)700部を入れ、80℃に液温を昇温
させた後、乾燥空気を少量通しながら滴下ロートから2
ヒドロキシ工チルアクリレート71部を2時間かけて滴
下し、滴下終了後さらK 80℃で3り時間反応を継続
した。
(A) Sample preparation Sample 1 A four-sided round bottom flask equipped with a stirrer, dropping funnel, temperature needle, reflux condenser, and dry air blowing tube had an average molecular weight of 1,
000, Ptadi≦-position of the polymer chain・092% is 1.2-
A urethane-modified derivative containing 3.6% free incyanate made from polybutadiene diol consisting of bonds (
Add 700 parts of Nl5SO-PBTL-1,000 (manufactured by Nippon Soda Co., Ltd., 50% ethyl acetate product), raise the temperature of the liquid to 80°C, and then add 700 parts of it from the dropping funnel while passing a small amount of dry air.
71 parts of hydroxyl engineered acrylate was added dropwise over 2 hours, and after the addition was completed, the reaction was continued for 3 hours at 80°C.

次に反応液を室温に冷却した後、酢酸エチル/トルエン
1/1の混合液71部を加えて樹脂濃度50%のコーテ
ィング樹脂試料(’/%1)を調整した。
Next, after the reaction solution was cooled to room temperature, 71 parts of a mixed solution of ethyl acetate/toluene 1/1 was added to prepare a coating resin sample ('/% 1) with a resin concentration of 50%.

また上記コーティング樹脂試料(41)100部に対し
、有機過酸化物(日本油脂■製パーへキサ3M)1部を
配合したコーティング樹脂試料〔/l6l−A)を調整
した。
In addition, a coating resin sample [/l6l-A] was prepared by blending 1 part of an organic peroxide (Perhexa 3M manufactured by NOF ■) with 100 parts of the above coating resin sample (41).

さらにコーティング樹脂試料(161)100部に対し
、有機過酸化物(日本油脂Iff#製 バーブチルZ)
1部、ナフテン酸コバルト(コバ/L−ト純分として)
001部を配合してコーティング樹脂試料〔/161−
B)調整した。
Furthermore, for 100 parts of the coating resin sample (161), an organic peroxide (Barbutyl Z manufactured by NOF Iff#) was added.
1 part, cobalt naphthenate (as pure cobalt/L-to)
Coating resin sample [/161-
B) Adjusted.

試料2 実施例1と同様な丸底フラスコに平均分子量1.000
、重合体鎖のブタジェン単位の92%が1.2−結合か
らなるポリブタジェンジカルボン酸を原料としたエポキ
シ変性誘導体(日本曹達社製Nl5SO−PB−:r−
ホ#シEPB−52M、 x−ホキシ当量2750)4
00部に対し、ジシアンジアミドo、4部ヲ加え、良(
かぎ混ぜて溶解し、コーティング樹脂試料〔A2)を調
整した。
Sample 2 An average molecular weight of 1.000 was placed in a round bottom flask similar to Example 1.
, an epoxy-modified derivative made from polybutadiene dicarboxylic acid in which 92% of the butadiene units in the polymer chain are 1,2-bonds (manufactured by Nippon Soda Co., Ltd., Nl5SO-PB-: r-
H #shi EPB-52M, x-hoxy equivalent weight 2750) 4
To 00 parts, add 4 parts of dicyandiamide o,
The mixture was stirred and dissolved to prepare a coating resin sample [A2].

試料3 平均分子量1,000で重合体鎖の192%が1.2−
結合からなるポリブタジェンジグリコールを原料とし、
溶媒と酸化剤および触媒の存在下で空気を導入して加熱
処理することにより部分酸化龜て得られる重合性樹脂(
日本曹達社製Nl5SO−PB −GQ −1,000
、固形分45%)25部に対しスチレン化アルキッド樹
脂(犬日本インキ化学工業社製スチレゾール4250、
固形分45%)75部を加え良くかき混ぜて均一に混合
溶解し、コーティング樹脂試料(、A3)を調整した。
Sample 3: With an average molecular weight of 1,000, 192% of the polymer chains are 1.2-
Made from polybutadiene diglycol consisting of bonds,
A polymeric resin obtained by partial oxidation by introducing air and heat treatment in the presence of a solvent, an oxidizing agent, and a catalyst.
Nippon Soda Co., Ltd. Nl5SO-PB -GQ -1,000
, solid content 45%) to 25 parts of styrenated alkyd resin (Styresol 4250 manufactured by Inu Nippon Ink Chemical Industry Co., Ltd.).
A coating resin sample (A3) was prepared by adding 75 parts (solid content: 45%) and stirring well to mix and dissolve uniformly.

試料4 試料3で用いた日本曹達社製Nl5SO−PB−αト1
.00080部に対し、ブチル化メラミン樹脂(大日本
インキイヒ学工業社製 スーパーベッカミンJ−820
、固形分60%)20部、6%ナフテン酸マンガン03
部を加え良くかぎ混ぜて均一に混合溶解し、コーティン
グ樹脂試料(A64)を調整した。
Sample 4 Nippon Soda Co., Ltd. Nl5SO-PB-αto1 used in Sample 3
.. 00080 parts, butylated melamine resin (Super Beckamine J-820 manufactured by Dainippon Ink Engineering Co., Ltd.)
, solid content 60%) 20 parts, 6% manganese naphthenate 03
A coating resin sample (A64) was prepared by adding a portion of the mixture and stirring well to mix and dissolve uniformly.

試料5 試料3で用いたNl5SO−PH−GQ −1,000
30部に対し、カーボンブラック15部を加えペイント
ローラーでよく混練して黒色エナメルミルベースを作成
し、これK Nl5SO−PB−(6)−1,0005
0部、スーパーベッカミンJ −820を20部を加え
良くかき混ぜて均一に混合溶解し、黒色コーティング樹
脂試料(AIL5 )を調整した。
Sample 5 Nl5SO-PH-GQ -1,000 used in sample 3
Add 15 parts of carbon black to 30 parts and knead well with a paint roller to create a black enamel mill base.
0 parts and 20 parts of Super Beckamine J-820 were added and stirred well to mix and dissolve uniformly to prepare a black coating resin sample (AIL5).

実施例1 試料1の調整で得られたコーティング樹脂試料(A 1
− A )中に薄葉紙(白州製紙■箔用原紙20 g/
m”、as μm )を浸漬し、紙繊維の内部に樹脂調
整液が浸透するように処理を行い、隙間間隔1露の2本
シゴキロールで余分な樹脂液をシゴキながら1ル努の速
度で引上げ、溶剤分′を揮発乾燥(45℃、N20分)
して厚さ200μmのコーティング樹脂フィルムCP−
1)を得た。
Example 1 Coating resin sample obtained in the preparation of sample 1 (A 1
- A) Thin paper (Hakushu Paper ■ base paper for foil 20 g/
m”, as μm), and treated so that the resin adjustment liquid penetrates into the inside of the paper fibers, and then pulled out at a speed of 1 roll while squeezing the excess resin liquid with two squeeze rolls with a gap of 1 roll. , evaporate and dry the solvent (45℃, N20 minutes)
Coating resin film CP- with a thickness of 200 μm
1) was obtained.

(膜厚は必要に応じて浸漬の繰返し、または塗布の繰返
しまたは浸漬と塗布の併用によっ−C調整)次’K、被
塗物としてラワンベニヤ板(150X50x3sm+)
の被塗面上に上記コーティング樹脂フィルムの樹脂層面
を重ね、その上K 50μmポリエステルフィルム(熱
プレスプレートと樹脂付着を防止のため)載せ、熱プレ
ス機を用いて表−IK示す条件で圧着し1熱融着塗装を
行った。
(The film thickness can be adjusted by repeating dipping, repeating coating, or combining dipping and coating as necessary.)Next, the object to be coated is a lauan plywood board (150 x 50 x 3 sm +)
Lay the resin layer side of the above coating resin film on the surface to be coated, place a K 50 μm polyester film (to prevent the resin from adhering to the heat press plate) on top of it, and press it using a heat press machine under the conditions shown in Table IK. 1 Heat fusion coating was applied.

上記塗装によって得られた塗装被塗物を室温で24時間
放置した後、試験片として塗膜性能を測定した。その結
果を表−IK示す。
After the coated object obtained by the above coating was left at room temperature for 24 hours, the coating film performance was measured as a test piece. The results are shown in Table IK.

実施例2 試料1で得られたコーティング樹脂試料〔腐1−B〕中
に実施例1と同様の薄葉紙を浸漬し、実施例1と同様の
処理を行ってコーティング樹脂フィルムを作成した後、
温風乾燥器で70℃×20分間硬化反応を促進した。次
に試料1で得られたコーティング樹脂試料〔/I61〕
中に浸漬し、隙間間li1%1.5 waのシゴキロー
ルで余分な樹脂液をシゴキながら1ル分の速度で引上げ
、溶剤分を揮発乾燥(45℃×20分)して厚さ300
μmのコーティング樹脂フィルム(P−2)を得た。
Example 2 A thin paper similar to that in Example 1 was immersed in the coating resin sample [Rot 1-B] obtained in Sample 1, and a coating resin film was created by performing the same treatment as in Example 1.
The curing reaction was accelerated in a hot air dryer at 70°C for 20 minutes. Next, the coating resin sample obtained in sample 1 [/I61]
The resin was immersed in the liquid and pulled up at a speed of 1 l while squeezing the excess resin liquid with a squeeze roll with a clearance of 1% 1.5 wa, and the solvent was evaporated and dried (45°C x 20 minutes) to a thickness of 300 mm.
A μm coating resin film (P-2) was obtained.

次に、上記コーティング樹脂フィルムを用い又実施例1
と全く同様に熱融着塗装を行い、その塗膜性能を測定し
、結果を表−IK示す。
Next, using the above coating resin film, Example 1
Heat fusion coating was carried out in exactly the same manner as above, and the coating performance was measured. The results are shown in Table IK.

実施例3 試料2で得られたコーティング樹°脂試料〔腐2〕中に
ガラヌクロス基材(■有沢製作所製EPC030)を浸
漬し、ガラス繊維の内部に樹脂調整液が浸透するように
処理を行い、実施例1と同じ操作、手順に従い、25℃
×24時間乾燥して膜厚300μmコーティング樹脂フ
ィルム(P−3)を得た。
Example 3 Galanucross base material (EPC030 manufactured by Arisawa Seisakusho) was immersed in the coating resin sample [Rot 2] obtained in Sample 2, and treated so that the resin conditioning liquid penetrated into the inside of the glass fiber. , following the same operations and procedures as in Example 1, at 25°C.
After drying for 24 hours, a coating resin film (P-3) having a thickness of 300 μm was obtained.

次に、上記コーティング樹脂フィルム、鋼板(磨鋼板J
IS −3141,150X 50 X O,3m )
を用いる他は実施例1と同様に表−IK示す条件で熱融
着塗装を行い、その塗膜性能を測定し、結果を表−1に
示す。
Next, the above coating resin film, steel plate (polished steel plate J
IS-3141, 150X 50X O, 3m)
Heat fusion coating was carried out under the conditions shown in Table IK in the same manner as in Example 1, except that the coating film performance was measured, and the results are shown in Table 1.

実施例4 試料3で得られたコーティング樹脂試料〔腐3〕中にボ
リエスル繊維不織布(日本バイリーン■H8103、厚
さ70μm)を浸漬し、以下実施例1と全く同じ操作、
手順に従ってフィルム厚さ300μmコーティング樹脂
フィルムのCP−4)を得た。
Example 4 A polyester fiber nonwoven fabric (Nippon Vilene H8103, thickness 70 μm) was immersed in the coating resin sample [Rotation 3] obtained in Sample 3, and the following operations were carried out in exactly the same manner as in Example 1.
A coated resin film CP-4) having a film thickness of 300 μm was obtained according to the procedure.

次に、上記コーティング樹脂フィルムを用い、実施例1
く全く同様にして熱融着塗装を行い、その塗膜性能を測
定し、結果を表−1に示す。
Next, using the above coating resin film, Example 1
Heat fusion coating was performed in exactly the same manner, and the coating performance was measured. The results are shown in Table 1.

実施例5 試料4で得られたコーティング樹脂試料〔腐4〕をシリ
コーン塗布したポリエステル剥離フィルム(藤森工業泗
1 バイナーシート 38E −C0IODW )上に
塗布L ”(120′c/20 分間乾燥シタ後、剥離
して厚さ150μmのフィルムを得た。次いでこのフィ
ルムの片面上にコーティング樹脂試料〔/161〕を塗
布、溶剤を揮発乾燥(45℃×20分)して合計膜厚2
00μmのコーティング樹脂フィルム(P−s)を得た
Example 5 The coating resin sample [Fu 4] obtained in Sample 4 was applied onto a silicone-coated polyester release film (Fujimori Kogyo 1 Biner Sheet 38E-C0IODW) after drying at 120'C/20 minutes. , to obtain a film with a thickness of 150 μm.Next, a coating resin sample [/161] was applied on one side of this film, and the solvent was evaporated and dried (45°C x 20 minutes) to give a total film thickness of 2
A coating resin film (Ps) of 00 μm was obtained.

次に、石綿スレート板(150X 50 X 3腫)の
被塗面に上記コーティング樹脂フィルムのコーティング
樹脂試料(41)樹脂層面を重ねる。以下実施例1と同
様に表−IK示す条件で熱融着塗装を行い、その塗膜性
能測定をし、結果を表−1に示す。
Next, the resin layer surface of the coating resin sample (41) of the coating resin film was placed on the coated surface of an asbestos slate board (150×50×3 size). Thermal adhesive coating was then carried out under the conditions shown in Table IK in the same manner as in Example 1, and the coating film performance was measured, and the results are shown in Table 1.

実施例6 試料5で得られた黒色コーティングエナメル樹脂試料(
I65)にオーバーレイ原紙(大福製紙■ 化粧板用オ
ーバーレイ原紙A)を浸漬し、以下実施例1と全く同じ
操作、手順に従って膜厚300μmの黒色コーティング
樹脂フィルム(P−6)を得た。
Example 6 Black coated enamel resin sample obtained in sample 5 (
Overlay base paper (Daifuku Paper Co., Ltd. Overlay base paper A for decorative boards) was immersed in I65), and the same operations and procedures as in Example 1 were followed to obtain a black coated resin film (P-6) with a thickness of 300 μm.

次に、上記コーティング樹脂フィルムを用いて実施例1
と全く同様にして熱融着塗装を行い、その塗膜性能を測
定し、結果を表−IK示す。
Next, Example 1 was prepared using the above coating resin film.
Heat fusion coating was carried out in exactly the same manner as above, and the coating film performance was measured, and the results are shown in Table IK.

手続補正書 昭和60年 3月JaL日 特許庁長官 志賀 学 殿 1、事件の表示 昭和59年特許願第38623号 2、発明の名称 熱融着塗装法 3、補正する者 事件との関係 特許出願人 8100東京都千代田区大手町2丁目2番1号(430
)日本曹達株式会社 代表者 三宮弐夫 4、代理人 8100東京都千代田区大手町2丁目2番1号日本曹達
株式会社内 電話 (245)6234 −0 1i1+ (71,25)横山吉美1− 明細書 発明の詳細な説明の欄 6、補正の内容 明細書中の発明の詳細な説明の欄を次の通り補正する。
Procedural amendment document March 1985 JaL Commissioner of the Japan Patent Office Manabu Shiga 1, Indication of the case Patent Application No. 38623 of 1988 2, Name of the invention Thermal fusion coating method 3, Person making the amendment Relationship with the case Patent application Person 8100 2-2-1 Otemachi, Chiyoda-ku, Tokyo (430
) Nippon Soda Co., Ltd. Representative Nippon Sannomiya 4, Agent 8100 2-2-1 Otemachi, Chiyoda-ku, Tokyo Nippon Soda Co., Ltd. Phone (245) 6234 -0 1i1+ (71,25) Yoshimi Yokoyama 1- Details Column 6 of Detailed Description of the Invention, Detailed Description of the Invention in the Description of Contents of the Amendment is amended as follows.

(11明細書第3頁第8行目の「塗装材料」を「被塗物
」に訂正する。
("Coating material" on page 3, line 8 of the 11 specification is corrected to "object to be coated."

(2) 同第3頁第11行目の「塗装方装」を「塗装方
法」に訂正する。
(2) "Painting method" on page 3, line 11 is corrected to "painting method."

(3)同第4頁第4行目の「予しめ」を「予め」に訂正
する。
(3) Correct "in advance" in the 4th line of page 4 to "in advance."

(4)同第6頁第11行目の「略儀」を「価格」に訂正
する。
(4) On page 6, line 11, ``Simplified'' is corrected to ``Price.''

(5) 同第9頁第6行目の「ニスチル」を「エステル
」に訂正する。
(5) "Nistil" in the 6th line of page 9 is corrected to "ester".

(61同第9頁第9行目の「一般的に」の次に「樹脂に
対して」を挿入する。
(Insert ``for resins'' after ``generally'' in the 9th line of page 9 of 61.

(7) 同第11頁第12行目の「2ヒドロキシ」を「
2−ヒドロキシ」に訂正する。
(7) Change “2-hydroxy” on page 11, line 12 of the same page to “
2-Hydroxy”.

(8)同第16頁第11行目の「ボリエスル」を「ポリ
エステル」に訂正する。
(8) On page 16, line 11 of the same page, "bolyesul" is corrected to "polyester."

(9) 同第19頁表の最上部の「表1」を「表=1」
に訂正する。
(9) “Table 1” at the top of the table on page 19 of the same page is “Table = 1”
Correct.

Claims (1)

【特許請求の範囲】[Claims] (1)フィルム状支持体の片面または両面に樹脂を塗布
して得られたコーティング樹脂フィルムを用い、該コー
ティング樹脂フィルムの樹脂層面を被塗物の表面にあて
て熱圧着することにより、コーティング樹脂を被塗面上
に融着せしめてフィルム状支持体を含む塗膜層を形成す
ることを特徴としてなる熱融着塗装法。
(1) Using a coating resin film obtained by applying a resin to one or both sides of a film-like support, the resin layer side of the coating resin film is applied to the surface of the object to be coated and bonded under heat, thereby applying the coating resin. A thermal fusion coating method characterized by fusion-bonding on a surface to be coated to form a coating layer containing a film-like support.
JP3862384A 1984-03-02 1984-03-02 Heat-fusing painting Pending JPS60183127A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3862384A JPS60183127A (en) 1984-03-02 1984-03-02 Heat-fusing painting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3862384A JPS60183127A (en) 1984-03-02 1984-03-02 Heat-fusing painting

Publications (1)

Publication Number Publication Date
JPS60183127A true JPS60183127A (en) 1985-09-18

Family

ID=12530363

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3862384A Pending JPS60183127A (en) 1984-03-02 1984-03-02 Heat-fusing painting

Country Status (1)

Country Link
JP (1) JPS60183127A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100421900C (en) * 2004-06-30 2008-10-01 上海瑞欣装饰材料有限公司 Method for producing high pressure decoration layer board of physiochemical thermosetting resin soaked paper

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100421900C (en) * 2004-06-30 2008-10-01 上海瑞欣装饰材料有限公司 Method for producing high pressure decoration layer board of physiochemical thermosetting resin soaked paper

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