JP2003276145A - Stainproof coated decorative material and method for manufacturing thereof - Google Patents

Stainproof coated decorative material and method for manufacturing thereof

Info

Publication number
JP2003276145A
JP2003276145A JP2002084661A JP2002084661A JP2003276145A JP 2003276145 A JP2003276145 A JP 2003276145A JP 2002084661 A JP2002084661 A JP 2002084661A JP 2002084661 A JP2002084661 A JP 2002084661A JP 2003276145 A JP2003276145 A JP 2003276145A
Authority
JP
Japan
Prior art keywords
layer
decorative
coating
undercoat layer
producing
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
JP2002084661A
Other languages
Japanese (ja)
Inventor
Mitsuo Ando
三津雄 安藤
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.)
Aica Kogyo Co Ltd
Original Assignee
Aica Kogyo 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 Aica Kogyo Co Ltd filed Critical Aica Kogyo Co Ltd
Priority to JP2002084661A priority Critical patent/JP2003276145A/en
Publication of JP2003276145A publication Critical patent/JP2003276145A/en
Pending legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To decompose a contaminant attaching to the surface of a decorative material by light. <P>SOLUTION: This decorative material is constituted of a decorative paper 2 bonded to a base material 1 and a urethane coated layer 5, a aqueous undercoat layer 6 and a photocatalytic layer 7 sequentially formed on the decorative surface. When the aqueous undercoat layer 6 is formed, the urethane coated layer 5 has no dry tack and is formed before its complete curing. <P>COPYRIGHT: (C)2003,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は光触媒機能を有する防汚
性塗装化粧材及びその製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antifouling coating cosmetic material having a photocatalytic function and a method for producing the same.

【0002】[0002]

【従来の技術】従来,光触媒機能を有する化粧材とし,
光触媒機能を有する酸化チタンと有機系バインダーを直
接接触しないカプセルタイプのものを用いたものが知ら
れている。また,PET,カーボネート,アクリル等の
フィルムにはフィルムの分解を防ぐアンダーコートを塗
布した上に光触媒層を設けた光触媒担持フィルムが知ら
れている。
2. Description of the Related Art Conventionally, a cosmetic material having a photocatalytic function is used.
It is known to use a capsule type that does not directly contact titanium oxide having a photocatalytic function with an organic binder. In addition, a photocatalyst-carrying film in which a photocatalyst layer is provided on a film of PET, carbonate, acrylic or the like, which is coated with an undercoat for preventing film decomposition, is known.

【0003】[0003]

【発明が解決しようとする課題】しかしながら,前者の
化粧材は,分解性,親水性といった全ての光触媒機能を
有するものではなく,後者の光触媒担持フィルムは全て
の触媒機能を有するものはあるが,光分解性を保持させ
るため支持基材のフィルムは透明であるため保護シート
としての機能に留まり,表面に意匠性がなく,色,柄を
コーディネートできないため住宅用としては不向きであ
った。また,化粧基材の意匠性を十分に引き出す方法と
してウレタン塗装を施す方法があるが,この塗装層の上
に全ての光触媒機能を付与する方法は見いだされていな
かった。
However, the former cosmetic material does not have all the photocatalytic functions such as degradability and hydrophilicity, while the latter photocatalyst-supporting film has all the catalytic functions, Since the film of the supporting base material is transparent in order to maintain photodegradability, it only functions as a protective sheet, and it is unsuitable for residential use because the surface has no design and the colors and patterns cannot be coordinated. Moreover, although there is a method of applying urethane coating as a method of sufficiently bringing out the designability of the decorative base material, a method of imparting all photocatalytic functions on this coating layer has not been found.

【0004】かような問題を解決する方法として,一般
的にウレタン塗装の上にアンダーコート層を形成し,更
に光触媒層を形成する方法を試みたものの,非水系のア
ンダーコート剤では,アンダーコートは容易に施せるが
光触媒機能が十分発揮されるものではなかった。
As a method for solving such a problem, a method of forming an undercoat layer on a urethane coating and then forming a photocatalyst layer is generally tried. Was easily applied, but the photocatalytic function was not sufficiently exhibited.

【0005】[0005]

【課題を解決するための手段】本発明はかかる状況に鑑
み検討されたもので,以下のことを特徴とするものであ
る。すなわち,基材に化粧紙が接着され,化粧表面に,
順次,ウレタン塗装層,水系アンダーコート層,光触媒
層が形成されてなることを特徴とする防汚性塗装化粧
材,基材に化粧紙を接着し,化粧表面に,順次,ウレタ
ン塗装層,水系アンダーコート層,光触媒層を形成する
ことを特徴とする防汚性塗装化粧材の製造方法,該水系
アンダーコート層を形成する際は,該ウレタン塗装層に
指触タックがなく,かつ,完全に硬化するまでの間に形
成することを特徴とする請求項2記載の防汚性塗装化粧
材の製造方法,前記指触タックがなく,かつ,完全に硬
化するまでの間を有機溶剤による光沢度の変化で判断し
て,該水系アンダーコート層を形成することを特徴とす
る請求項3記載の防汚性塗装化粧材の製造方法,前記光
沢度の変化を示す度合いを式1で示される指数とするこ
とを特徴とする請求項4記載の防汚性塗装化粧材の製造
方法,
The present invention has been studied in view of the above situation, and is characterized by the following. That is, the decorative paper is adhered to the base material, and the decorative surface is
A urethane coating layer, a water-based undercoat layer, and a photocatalyst layer are formed in that order, and an antifouling coating material is applied to the base material. A method for producing an antifouling coating decorative material characterized by forming an undercoat layer and a photocatalyst layer, and when forming the water-based undercoat layer, the urethane coating layer has no finger tack and is completely 3. The method for producing an antifouling coating decorative material according to claim 2, wherein it is formed before being cured, and the glossiness of the organic solvent is free from the finger-tacking and completely curing. The method for producing an antifouling coating cosmetic material according to claim 3, wherein the water-based undercoat layer is formed according to the change in the index, and the degree of change in the glossiness is an index represented by the formula 1. Claims characterized by 4 antifouling method for producing a coated decorative material according,

【式1】 該指数が0.9以下の時に該水系アンダーコート層を形
成することを特徴とする請求項5記載の防汚性塗装化粧
材の製造方法,である。以下,本発明について詳細に説
明する。
[Formula 1] The method for producing an antifouling coating decorative material according to claim 5, wherein the water-based undercoat layer is formed when the index is 0.9 or less. Hereinafter, the present invention will be described in detail.

【0006】本発明の防汚性塗装化粧材は,合板,木
材,MDF等の木質系基板,熱硬化性樹脂積層板などの
基材に,熱硬化性樹脂化粧板用に供される坪量80〜1
40g/m2の化粧紙や,プリント合板用に供される坪
量20〜40g/m2の薄葉紙など通常公知のものを接
着し,順次,サンディングシーラーを塗布して,塗装を
施して,水系アンダーコート層を設け,更に光触媒層を
形成したものである。
The antifouling coating decorative material of the present invention is used as a base material such as plywood, wood, wood-based substrate such as MDF, thermosetting resin laminated board, etc. 80-1
40 g / m 2 decorative paper or thin paper with a basis weight of 20 to 40 g / m 2 used for printed plywood is adhered, and then a sanding sealer is applied in sequence, followed by painting An undercoat layer is provided and a photocatalyst layer is further formed.

【0007】熱硬化性樹脂積層板としては,例えばメラ
ミン樹脂含浸紙とフェノール樹脂含浸紙とを通常公知の
方法で熱圧成形したメラミン樹脂化粧板,メラミン樹脂
含浸紙を同様の方法で熱圧成形したメラミン樹脂積層
板,フェノール樹脂含浸紙を同様の方法で熱圧成形した
フェノール樹脂積層板などが挙げられ,化粧紙,壁面な
どの下地との接着性を考慮して表裏両面をサンディング
処理する。
As the thermosetting resin laminate, for example, melamine resin-impregnated paper and melamine resin-impregnated paper obtained by thermocompression molding of melamine resin-impregnated paper and phenol resin-impregnated paper by a conventionally known method are thermocompression-molded by the same method. Examples include melamine resin laminates, phenolic resin-impregnated papers thermoformed by the same method, and phenol resin laminates. Sanding treatment is applied to both the front and back surfaces in consideration of adhesion to decorative paper, wall and other substrates.

【0008】ウレタン塗装に用いるポリウレタンは,一
般に市販されているポリオールをイソシアネート系硬化
剤で硬化させるタイプで液状のものであればよく,特に
制約はない。
The polyurethane used for urethane coating is not particularly limited as long as it is a liquid type which is a type in which a commercially available polyol is cured with an isocyanate curing agent.

【0009】アンダーコート層は,光触媒を固着するた
めのバインダーであり,このバインダーとしては,少な
くともシリコンを二酸化ケイ素換算で2重量%〜60重
量%含有するシリコン変性樹脂,コロイダルシリカを二
酸化ケイ素換算で5重量%〜40重量%含有する樹脂,
ポリシロキサンを二酸化ケイ素換算で3重量%〜60重
量%含有する樹脂や,あるいはアルカリ金属シリカ化合
物又はこのアルカリ金属シリカ化合物を含有するアモル
ファス型過酸化チタンゾル,アモルファス型酸化チタン
ゾルもしくはアモルファス型チタン水酸化物,光触媒能
を有さないアモルファス型過酸化チタン及び/又はアモ
ルファス型酸化チタンなどを水分散エマルジョンに混合
したものが挙げられる。
The undercoat layer is a binder for fixing the photocatalyst, and as the binder, a silicon-modified resin containing at least 2 to 60% by weight of silicon in terms of silicon dioxide, and colloidal silica in terms of silicon dioxide. Resin containing 5% to 40% by weight,
Resin containing 3 wt% to 60 wt% of polysiloxane in terms of silicon dioxide, or alkali metal silica compound or amorphous titanium peroxide sol, amorphous titanium oxide sol or amorphous titanium hydroxide containing the alkali metal silica compound , An amorphous titanium peroxide having no photocatalytic ability and / or an amorphous titanium oxide mixed with an aqueous dispersion emulsion.

【0010】アンダーコート層に非水系である溶剤タイ
プシリコーン樹脂を用いると下地のウレタン塗装層とな
じみがよく,概ね密着性は悪くないものの,表1の比較
例2,3,4に示すように光触媒分解性が劣り好ましく
ない。
When a non-aqueous solvent type silicone resin is used for the undercoat layer, it has good compatibility with the underlying urethane coating layer and the adhesiveness is not bad in general, but as shown in Comparative Examples 2, 3 and 4 of Table 1. Photocatalytic degradability is inferior, which is not preferable.

【0011】アンダーコート層を形成する際は下地のウ
レタン塗装層が指触タックがなく,かつ,完全に硬化す
るまでの間に塗布するのが重要で,指触タックのある状
態で塗布するとウレタン塗料と混ざり合い光触媒の固着
が不充分となりやすく,また,完全に硬化した後に塗布
すると,はじかれてアンダーコート層が形成されないと
いう不都合が生じる。この適度な状態はウレタン塗装を
施した後,完全に硬化するまでの間に有機溶剤により塗
膜が侵される性質を利用して判断することができ,塗装
後のウレタン塗装層の光沢度と,ジオキサン,ジメチル
フォルムアミド,ジメチルスルフォンオキサイドなど塗
膜を侵食しやすい有機溶剤で処理した後の光沢度とを比
較することにより判断でき,式1の指数が0.9以下が
好ましい。この値が0.9を超えると塗膜の濡れ性が悪
くなる結果,密着性が劣り光触媒を固着できなくなり光
触媒分解性が劣りやすくなる。
When the undercoat layer is formed, it is important to apply it before the urethane coating layer as the base has no finger touch tack and is completely cured. If it is applied with the finger touch tack, urethane is applied. The photocatalyst is liable to be insufficiently fixed due to mixing with the paint, and when the photocatalyst is completely cured and then applied, it is repelled and the undercoat layer is not formed. This proper state can be judged by utilizing the property that the coating film is corroded by the organic solvent after the urethane coating is applied and before it is completely cured. The glossiness of the urethane coating layer after coating, It can be judged by comparing with the glossiness after the coating film is treated with an organic solvent which easily corrodes dioxane, dimethylformamide, dimethylsulfone oxide, and the index of the formula 1 is preferably 0.9 or less. If this value exceeds 0.9, the wettability of the coating film deteriorates, and as a result, the adhesion becomes poor and the photocatalyst cannot be fixed, and the photocatalytic decomposability tends to become poor.

【0012】[0012]

【式1】 [Formula 1]

【0013】光触媒層を形成するために用いる光触媒コ
ーテング剤は,前述のバインダーに光触媒を混合させた
もので,光触媒は,特定の波長の光が照射されると光化
学反応を起こすことにより有機物を分解する触媒として
作用したり,抗菌または防黴作用等の働きが得られる金
属酸化物のことをいい,例えば,酸化チタン(Ti
2),酸化亜鉛(ZnO),酸化錫(SnO),チタ
ン酸ストロンチウム(SrTiO3),酸化セリウム
(CeO),酸化鉄(Fe23)等が挙げられ,これら
の酸化物のうち,太陽光や日常生活で用いられる照明光
で高い触媒活性を有する酸化チタンがとりわけ望まし
い。
The photocatalyst used to form the photocatalyst layer
As the coating agent, the photocatalyst was mixed with the above-mentioned binder.
Photocatalysts become photocatalytic when they are irradiated with light of a specific wavelength.
As a catalyst that decomposes organic substances by causing biological reactions
Gold that acts and has an antibacterial or antifungal effect
Refers to group oxides such as titanium oxide (Ti
O 2), Zinc oxide (ZnO), tin oxide (SnO), titanium
Strontium acid salt (SrTiO 33), Cerium oxide
(CeO), iron oxide (Fe2O3), Etc., and these
Of the oxides of the sun, illumination light used in daily life and daily life
And titanium oxide with high catalytic activity is particularly desirable.
Yes.

【0014】酸化チタンとしてはルチル型酸化チタン,
アナターゼ型酸化チタン,フルッカイト型酸化チタンな
どが例示されるが,アナターゼ型の方が入手しやすく安
価で特性が安定しており,かつ,人体に無害であり,光
触媒として優れた効果を発揮し好ましい。
As titanium oxide, rutile type titanium oxide,
Examples of anatase type titanium oxide, fluccite type titanium oxide and the like are preferable, and the anatase type titanium oxide is easier to obtain, cheaper and stable in characteristics, harmless to the human body, and excellent in a photocatalyst effect, which is preferable. .

【0015】以下,本発明を実施例,比較例に基づいて
詳細に説明する。
The present invention will be described in detail below based on Examples and Comparative Examples.

【実施例】実施例1 基材として厚み2.5mmの合板を用い,酢酸ビニル系
接着剤を38g/m2塗布して80g/m2の白系の化粧
紙を接着した。次いで,サンディングシーラーとして二
液硬化型ウレタン系樹脂(浜二ペイント株式会社製 商
品名Uコートサンジング)を塗布した後,フローコータ
ーで二液硬化型ウレタン系樹脂(サンユーペイント株式
会社製 商品名 ウレタンフラット)を塗布量が100
g/m2となるように塗布し,乾燥させて,ウレタン塗
装層を形成し,指触タックがなくなった後,60゜入射
角光沢度計の光沢値を測定し,ウレタン塗装層の一部を
ジオキサンで5分処理した後,光沢値を測定し,式2で
示す指数が0.5になった時,アンダーコート剤として
アクリルシリコン樹脂エマルジョン(チタン工業株式会
社製 PCU−103)を10μ塗布した。次いで,酸
化チタン光触媒塗料(チタン工業株式会社製 PC−4
01)1μ塗布して,実施例1の防汚性塗装化粧材を得
た。
Using plywood thickness 2.5mm as EXAMPLE 1 substrate, bonding the decorative paper of whitish of 80 g / m 2 of vinyl acetate-based adhesive 38 g / m 2 coated with. Next, after applying a two-component curing type urethane resin (trade name U-coat sanding manufactured by Hamani Paint Co., Ltd.) as a sanding sealer, a two-component curing type urethane resin (trade name urethane manufactured by Sanyu Paint Co., Ltd.) is applied using a flow coater. Flat) coating amount is 100
Apply the coating to g / m 2 and dry to form a urethane coating layer. After the tack on the finger is removed, measure the gloss value of a 60 ° incident angle gloss meter and measure the urethane coating layer. Was treated with dioxane for 5 minutes, the gloss value was measured, and when the index shown in Formula 2 was 0.5, 10 μm of acrylic silicone resin emulsion (PCU-103 manufactured by Titanium Industry Co., Ltd.) was applied as an undercoat agent. did. Next, titanium oxide photocatalyst paint (PC-4 manufactured by Titanium Industry Co., Ltd.)
01) 1 μ was applied to obtain the antifouling coating decorative material of Example 1.

【式2】 [Formula 2]

【0016】実施例2 実施例1において,二液硬化型ウレタン系樹脂の硬化を
進行させ,式2の指数が0.9の時にアンダーコート層
を形成した以外は同様に実施して,実施例2の防汚性塗
装化粧材を得た。
Example 2 The same procedure as in Example 1 was carried out except that the curing of the two-component curing type urethane resin was advanced and the undercoat layer was formed when the index of the formula 2 was 0.9. The antifouling coating decorative material 2 was obtained.

【0017】比較例1 実施例1において,二液硬化型ウレタン系樹脂の硬化を
進行させ,式2の指数が1.0の時にアンダーコート層
を形成した以外は同様に実施して,比較例1の化粧材を
得た。
Comparative Example 1 Comparative Example 1 was carried out in the same manner as in Example 1 except that the two-component curing type urethane resin was cured and the undercoat layer was formed when the index of the formula 2 was 1.0. A cosmetic material of No. 1 was obtained.

【0018】比較例2 実施例1において,アンダーコート層として溶剤タイプ
シリコン樹脂系プライマーを使用した以外は同様に実施
して比較例2の化粧材を得た。
Comparative Example 2 A decorative material of Comparative Example 2 was obtained in the same manner as in Example 1 except that a solvent type silicone resin primer was used as the undercoat layer.

【0019】比較例3 実施例2において,アンダーコート層として溶剤タイプ
シリコン樹脂系プライマーを使用した以外は同様に実施
して比較例3の化粧材を得た。
Comparative Example 3 A decorative material of Comparative Example 3 was obtained in the same manner as in Example 2, except that a solvent type silicone resin-based primer was used as the undercoat layer.

【0020】比較例4 比較例1において,アンダーコート層として溶剤タイプ
シリコン樹脂系プライマーを使用した以外は同様に実施
して比較例4の化粧材を得た。
Comparative Example 4 A decorative material of Comparative Example 4 was obtained in the same manner as in Comparative Example 1, except that a solvent type silicone resin-based primer was used as the undercoat layer.

【0021】評価結果を表1に示す。The evaluation results are shown in Table 1.

【表1】 [Table 1]

【0022】評価方法については以下の通りとした。 アンダーコート層形成時のはじき アンダーコ−ト剤を塗布した時の状態を目視にて判断
し,ハジキのないもの○,ハジキはあるが,外観では判
らないもの△,光触媒コーティング剤を塗布した後も欠
点があらわれるもの×,とした。 光触媒・アンダーコート密着性 実施例1,2の防汚性塗装化粧材,比較例1〜4の塗装
化粧材にセロハンテープを密着させ,剥離後の状態を観
察し,剥離のないものを○,10%未満の剥離部分があ
るものを△,10%以上の剥離部分があるものを×とし
た。 光触媒分解機能 実施例1,2の防汚性塗装化粧材,比較例1〜4の塗装
化粧材に,20倍希釈の赤インクを塗布し,色測計にて
Labを測定し,10Wブラックライト10cm直下に
2時間曝し,Labを測定して色差ΔEを求めた。ΔE
が15以上を○,ΔEが3〜15を△,ΔEが3未満を
×とした。
The evaluation method was as follows. Repelling when forming the undercoat layer By visually observing the state when the undercoating agent is applied, there is no cissing ○, there is cissing but it is not visible in the appearance △, even after applying the photocatalytic coating agent It is said that there are defects. Photocatalyst / Undercoat Adhesion The cellophane tape was adhered to the antifouling coating decorative materials of Examples 1 and 2 and the coating decorative materials of Comparative Examples 1 to 4, and the state after peeling was observed. When there was less than 10% of the peeled portion, Δ was given, and when there was more than 10% of the peeled portion, x was given. Photocatalytic decomposition function A 20-fold diluted red ink was applied to the antifouling coating decorative materials of Examples 1 and 2 and the coating decorative materials of Comparative Examples 1 to 4, and Lab was measured with a colorimeter to obtain 10W black light. The sample was exposed to 10 cm immediately below for 2 hours, and the Lab was measured to determine the color difference ΔE. ΔE
Is 15 or greater, ΔE is 3 to 15, and ΔE is less than 3.

【0023】[0023]

【発明の効果】本発明ではウレタン塗料の硬化状態の判
定として,有機溶剤を用い光沢度の比率を式1に示す指
数とし,この指数が0.9以下の状態の時に,アンダー
コート層として水系のものを塗布することにより,外
観,密着,光触媒分解の良好な防汚性塗装化粧材を得る
ことができる。
EFFECT OF THE INVENTION In the present invention, as a determination of the curing state of a urethane coating, an organic solvent is used and the ratio of glossiness is used as an index shown in Formula 1. When this index is 0.9 or less, the undercoat layer is water-based. By applying the above, it is possible to obtain an antifouling coating decorative material with good appearance, adhesion, and photocatalytic decomposition.

【図面の簡単な説明】[Brief description of drawings]

【図1】 実施例1の防汚性塗装化粧材の構成断面図。FIG. 1 is a cross-sectional configuration diagram of an antifouling coating decorative material of Example 1.

【符号の説明】[Explanation of symbols]

1 基材 2 化粧紙 5 ウレタン塗装層 6 水系アンダーコート層 7 光触媒層 10 防汚性塗装化粧材 1 base material 2 Decorative paper 5 Urethane coating layer 6 Water-based undercoat layer 7 Photocatalyst layer 10 Antifouling paint cosmetics

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C09D 5/00 C09D 5/00 Z 175/04 175/04 E04F 13/08 E04F 13/08 A Fターム(参考) 2E110 AA37 AA65 AB22 BA05 BB04 EA09 GA06W GB53Z 4D075 AE06 BB25Y BB91Y CA13 CA34 DA06 DB18 DB22 DB25 DB46 DB63 DC01 DC31 EA06 EA13 EB38 EB43 EC02 4F100 AA17E AA21 AK22G AK25 AK51C AK52 AP02 AT00A BA05 BA07 BA10A BA10E CC00C CC00D DG10B EH46 EH462 EJ08 EJ082 EJ65D HB00B JK06 JL06 JL08E JL11 JM02 JN21 YY00 4J038 DG051 DG231 DL031 HA146 HA216 MA08 MA10 NA05 PA07 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) C09D 5/00 C09D 5/00 Z 175/04 175/04 E04F 13/08 E04F 13/08 A F term ( reference) 2E110 AA37 AA65 AB22 BA05 BB04 EA09 GA06W GB53Z 4D075 AE06 BB25Y BB91Y CA13 CA34 DA06 DB18 DB22 DB25 DB46 DB63 DC01 DC31 EA06 EA13 EB38 EB43 EC02 4F100 AA17E AA21 AK22G AK25 AK51C AK52 AP02 AT00A BA05 BA07 BA10A BA10E CC00C CC00D DG10B EH46 EH462 EJ08 EJ082 EJ65D HB00B JK06 JL06 JL08E JL11 JM02 JN21 YY00 4J038 DG051 DG231 DL031 HA146 HA216 MA08 MA10 NA05 PA07

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 基材に化粧紙が接着され,化粧表面に,
順次,ウレタン塗装層,水系アンダーコート層,光触媒
層が形成されてなることを特徴とする防汚性塗装化粧
材。
1. A decorative paper is adhered to a base material, and the decorative surface is
An antifouling paint decorative material comprising a urethane coating layer, a water-based undercoat layer, and a photocatalyst layer sequentially formed.
【請求項2】 基材に化粧紙を接着し,化粧表面に,順
次,ウレタン塗装層,水系アンダーコート層,光触媒層
を形成することを特徴とする防汚性塗装化粧材の製造方
法。
2. A method for producing an antifouling coating cosmetic material, which comprises adhering a decorative paper to a base material and sequentially forming a urethane coating layer, an aqueous undercoat layer and a photocatalyst layer on the decorative surface.
【請求項3】 該水系アンダーコート層を形成する際
は,該ウレタン塗装層に指触タックがなく,かつ,完全
に硬化するまでの間に形成することを特徴とする請求項
2記載の防汚性塗装化粧材の製造方法。
3. The protective coating according to claim 2, wherein when the water-based undercoat layer is formed, the urethane coating layer has no finger tack and is formed before it is completely cured. Method for manufacturing stain-resistant coating material.
【請求項4】 前記指触タックがなく,かつ,完全に硬
化するまでの間を有機溶剤による光沢度の変化で判断し
て,該水系アンダーコート層を形成することを特徴とす
る請求項3記載の防汚性塗装化粧材の製造方法。
4. The water-based undercoat layer is formed by judging the change in glossiness due to an organic solvent until there is no tackiness on the finger and complete curing. A method for producing the antifouling coating material as described.
【請求項5】 前記光沢度の変化を示す度合いを式1で
示される指数とすることを特徴とする請求項4記載の防
汚性塗装化粧材の製造方法。 【式1】
5. The method for producing an antifouling coating decorative material according to claim 4, wherein the degree of the change in the glossiness is set as an index represented by Formula 1. [Formula 1]
【請求項6】 該指数が0.9以下の時に該水系アンダ
ーコート層を形成することを特徴とする請求項5記載の
防汚性塗装化粧材の製造方法。
6. The method for producing an antifouling coating material according to claim 5, wherein the water-based undercoat layer is formed when the index is 0.9 or less.
JP2002084661A 2002-03-26 2002-03-26 Stainproof coated decorative material and method for manufacturing thereof Pending JP2003276145A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002084661A JP2003276145A (en) 2002-03-26 2002-03-26 Stainproof coated decorative material and method for manufacturing thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002084661A JP2003276145A (en) 2002-03-26 2002-03-26 Stainproof coated decorative material and method for manufacturing thereof

Publications (1)

Publication Number Publication Date
JP2003276145A true JP2003276145A (en) 2003-09-30

Family

ID=29207044

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002084661A Pending JP2003276145A (en) 2002-03-26 2002-03-26 Stainproof coated decorative material and method for manufacturing thereof

Country Status (1)

Country Link
JP (1) JP2003276145A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004291262A (en) * 2003-03-25 2004-10-21 Aica Kogyo Co Ltd Anti-staining decorative sheet
JP2008253942A (en) * 2007-04-06 2008-10-23 Kubota Matsushitadenko Exterior Works Ltd Building plate
JP2018508606A (en) * 2015-02-11 2018-03-29 アライド バイオサイエンス, インコーポレイテッド Antimicrobial coating and method for forming it

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004291262A (en) * 2003-03-25 2004-10-21 Aica Kogyo Co Ltd Anti-staining decorative sheet
JP2008253942A (en) * 2007-04-06 2008-10-23 Kubota Matsushitadenko Exterior Works Ltd Building plate
JP2018508606A (en) * 2015-02-11 2018-03-29 アライド バイオサイエンス, インコーポレイテッド Antimicrobial coating and method for forming it

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