JPH01272672A - Coating composition - Google Patents

Coating composition

Info

Publication number
JPH01272672A
JPH01272672A JP10188188A JP10188188A JPH01272672A JP H01272672 A JPH01272672 A JP H01272672A JP 10188188 A JP10188188 A JP 10188188A JP 10188188 A JP10188188 A JP 10188188A JP H01272672 A JPH01272672 A JP H01272672A
Authority
JP
Japan
Prior art keywords
coating
film
coating composition
colored
paint
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
JP10188188A
Other languages
Japanese (ja)
Inventor
Osamu Kuramitsu
修 倉光
Kashi Fujimoto
藤本 樫
Tateki Maikuma
毎熊 干城
Fumiaki Kobayashi
文明 小林
Shinji Noguchi
晋治 野口
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP10188188A priority Critical patent/JPH01272672A/en
Publication of JPH01272672A publication Critical patent/JPH01272672A/en
Pending legal-status Critical Current

Links

Landscapes

  • Paints Or Removers (AREA)

Abstract

PURPOSE:To obtain the coating composition for protective coating of illuminator component, etc., containing a coloring substance and capable of forming colorless and transparent coating film after coating and checking film thickness by a shade of color of coating composition on a product to be coated. CONSTITUTION:The aimed composition, e. g., obtained by adding (B) an acid- base indicator (e.g., pentamethoxy red) capable of coloring in acidity and (C) an acidic reagent (e. g., hydrochloric acid) to (A) coating composition, capable of readily providing an uniform transparent protection film, because of being able to carry out coating while controlling film thickness of coating film and usable for various raw materials to be coated such as metal, paper, etc.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、透明な塗膜を形成する塗料組成物に関する
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] This invention relates to a coating composition that forms a transparent coating film.

〔従来の技術〕[Conventional technology]

従来、照明器具の装飾等に使用されるメツキ部品(たと
えば、フランジ、アーム等)や反射板等には、耐食性を
付与するための保護コートが施されている。この保護コ
ートには、一般に、被塗物の光学的特性に影響を及ぼさ
ないよう、透明な塗料が用いられ、透明な塗膜が形成さ
れるようになっている。
Conventionally, plated parts (eg, flanges, arms, etc.), reflectors, and the like used for decoration of lighting equipment have been coated with a protective coat to impart corrosion resistance. Generally, a transparent paint is used for this protective coat so as not to affect the optical properties of the object to be coated, so that a transparent coating film is formed.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

ところが、保護コート用塗料が透明であることから、上
記メツキ部品や反射板等に均一な塗膜を形成するのは容
易なことではな(、塗装作業者には高度な熟練が要求さ
れる。仮に、保護コートの膜厚が不均一になってしまう
と、メツキ部品の変色や、反射板の反射率の低下等につ
ながりかねないため、好ましくない。
However, since the protective coating paint is transparent, it is not easy to form a uniform coating on the plated parts, reflectors, etc. (and requires a high level of skill from the painter. If the thickness of the protective coat were to become non-uniform, this would be undesirable because it could lead to discoloration of the plated parts and a decrease in the reflectance of the reflector.

保護コートの膜厚を管理する方法としては、膜厚計(う
ず電流方式、超音波方式等)による接触測定を行うこと
が考えられるが、下記のような問題点を孕んでいること
から、実用的ではない。
One possible way to control the film thickness of the protective coat is to perform contact measurement using a film thickness meter (eddy current method, ultrasonic method, etc.), but it is not practical due to the following problems. Not the point.

■ 部品全体を1箇所、1箇所測定する必要があるため
、非常に手間がかかり、不良箇所の検出精度および測定
効率に問題がある。
■ Since it is necessary to measure the whole part one by one, it is very time-consuming and there are problems with the detection accuracy and measurement efficiency of defective parts.

■ 塗膜の膜厚測定は、塗膜が硬化した後でなければ行
うことができず、塗装時点で膜厚のバラツキをチエツク
することができない。
■ The thickness of the paint film can only be measured after the paint film has hardened, and it is not possible to check for variations in film thickness at the time of painting.

以上の事情に鑑み、この発明は、透明な塗膜を形成する
塗料組成物ではあるが、塗装時には着色していることに
より、目視等により膜厚をチエ。
In view of the above circumstances, the present invention is a coating composition that forms a transparent coating film, but because it is colored at the time of coating, it is difficult to check the film thickness by visual inspection or the like.

りしつつ塗装できるような新規な塗料組成物を提供する
ことを課題とする。
An object of the present invention is to provide a new coating composition that can be painted while maintaining the same properties.

〔課題を解決するだめの手段〕[Failure to solve the problem]

上記課題を解決するため、この発明は、着色物質を含み
塗装時には着色している塗料組成物において、前記着色
物質が塗装ののちに無色に変わるか塗膜中から消失する
ことにより、透明な塗膜を形成するようになっている。
In order to solve the above-mentioned problems, the present invention provides a coating composition that contains a colored substance and is colored at the time of coating. It is designed to form a film.

〔作   用〕[For production]

この発明にかかる塗料組成物は、着色物質を含んだ有色
のものであるため、被塗物」二の塗料組成物の色の濃淡
等により膜厚をチエツクしつつ、これの塗装を行うこと
ができる。そし2で、この着色物質は、塗装ののち無色
に変わる、あるいは、塗膜中から消失するものであるた
め、最終的には無色透明な塗膜が形成される。
Since the coating composition according to the present invention is colored and contains a coloring substance, it is possible to apply the coating while checking the film thickness by checking the color shading of the coating composition on the object to be coated. can. In step 2, this colored substance turns colorless or disappears from the coating film after painting, so that a colorless and transparent coating film is ultimately formed.

〔実 施 例〕〔Example〕

まず、この発明にかかる塗料組成物に含まれる着色物質
について説明する。この着色物質は、塗装後、最終的に
無色に変わるか塗膜中から消失するものであって、透明
な塗膜の形成を可能によるものであれば、特に限定はさ
れない。たとえば、具体的には、下記のようなタイプに
分類することができる。
First, the coloring substance contained in the coating composition according to the present invention will be explained. This colored substance is not particularly limited as long as it ultimately turns colorless or disappears from the coating film after coating, and is capable of forming a transparent coating film. For example, specifically, it can be classified into the following types.

(A)  室温では着色しているが、高温(塗料の焼付
は温度)になると無色透明に変化し、その後室温に戻っ
てもそのままの状態を保つ(不可逆変化)もの。あるい
は、経時的に有色から無色へ、不可逆的に変化するもの
(A) A substance that is colored at room temperature, but turns colorless and transparent at high temperatures (the temperature at which paint bakes), and then remains that way even when the temperature returns to room temperature (an irreversible change). Or something that changes irreversibly from colored to colorless over time.

(Bl  塗装後、塗膜が硬化する際等に、分解、藤発
(揮発)あるいは胃華し、硬化塗膜中から消失するもの
(Bl) When the paint film is cured after painting, it decomposes, evaporates (volatizes), or evaporates, and disappears from the cured paint film.

(0酸化あるいは還元反応により、無色透明になるもの
(0) Something that becomes colorless and transparent due to oxidation or reduction reactions.

(D)  低沸点の着色溶剤。(D) Low boiling point colored solvent.

以下に、上記各タイプについて、さらに詳しく説明する
。はじめに、上記(Nタイプとしては、たとえば、酸性
で発色する指示薬と、加熱により蒸発する酸性試薬(た
とえば塩酸等)との組み合わせが挙げられる。この指示
薬は、酸性領域に変色域を有する酸塩基指示薬であり、
酸性色は有色。
Each of the above types will be explained in more detail below. First, the above (N type) includes, for example, a combination of an indicator that develops color under acidity and an acidic reagent (such as hydrochloric acid) that evaporates when heated. This indicator is an acid-base indicator that has a color change region in the acidic region. and
Acidic colors are colored.

中性付近では無色のもの(たとえばペンタメトキシレッ
ド、ヘキサノ[・キシレッド等)である。上記両者を塗
料に添加すれば、酸性の着色塗料が調製され、塗装時に
は指示薬の酸性色があられれて着色している。しかし、
加熱等により酸性試薬が蒸発すれば、指示薬の酸性色が
消失して無色の中性色があられれるため、出来上がりの
塗膜は無色透明なものとなる。反対に、アルカリ性で発
色する指示薬を、アルカリ性試薬(たとえばアンモニア
水等)と組み合わせて用いることも同様に可能である。
Near neutrality, it is colorless (for example, pentamethoxy red, hexano[xy red, etc.). If both of the above are added to a paint, an acidic colored paint is prepared, and the acidic color of the indicator is abraded during painting, resulting in coloring. but,
When the acidic reagent is evaporated by heating or the like, the acidic color of the indicator disappears and a colorless neutral color is formed, so that the finished coating film becomes colorless and transparent. Conversely, it is also possible to use an indicator that develops color under alkalinity in combination with an alkaline reagent (for example, aqueous ammonia).

この場合の指示薬は、塩基性色が有色。In this case, the basic color of the indicator is colored.

中性色が無色で、アルカリ性領域に変色域を有する酸塩
基指示薬(たとえばフェノールフタレイン、O−クレゾ
ールフタレイン、チモールフタレイン等)である。
It is an acid-base indicator that is colorless as a neutral color and has a color change region in an alkaline region (for example, phenolphthalein, O-cresol phthalein, thymol phthalein, etc.).

つぎに、上記(9)り・イブとしては、たとえば、カル
ミン酸、1.2−ナフトキノン、O−ベンゾキノンのよ
うな、常温では安定な着色化合物であるが、高温になる
と分解して無色透明になるものが挙げられる。また、温
度変化によらなくても経時的に分解していくような着色
化合物であってもよい。
Next, the above (9) Ri-ib is a colored compound that is stable at room temperature, such as carminic acid, 1,2-naphthoquinone, and O-benzoquinone, but decomposes at high temperatures and becomes colorless and transparent. There are several things that can be mentioned. Alternatively, it may be a colored compound that decomposes over time without being affected by temperature changes.

上記(aタイプには、たとえば、酸化(あるいは還元)
により無色になる指示薬(酸化還元指示薬)と、加熱等
により酸化剤(あるいは還元剤)となる試薬との組み合
わせが挙げられる。両者を塗料に添加すれば、焼付は時
等の酸化剤または還元剤の作用を受けて、指示薬の色は
消失される。そのような指示薬とし゛ては、トリス(ジ
ピリジル)fi (II) l化物2メチレンブルー、
ジフェニルアミン等が例示できる。
The above (type a includes, for example, oxidation (or reduction)
Examples include a combination of an indicator that becomes colorless (oxidation-reduction indicator) when heated, and a reagent that becomes an oxidizing agent (or reducing agent) when heated or the like. When both are added to the paint, the color of the indicator disappears due to the action of the oxidizing agent or reducing agent during baking. Such indicators include tris(dipyridyl)fi(II) chloride 2 methylene blue;
Examples include diphenylamine.

さらに、上記の)タイプとしては、2−アミノチオフェ
ン(沸点62℃)、N−ニトロソ−N−メチルウレタン
(沸点65〜65.5℃)等が挙げられる。これらの着
色した低沸点溶剤を添加しておけば、塗装後にこれらが
蕪発し、透明な塗膜が得られる。
Furthermore, examples of the above type include 2-aminothiophene (boiling point: 62°C), N-nitroso-N-methylurethane (boiling point: 65 to 65.5°C), and the like. If these colored low boiling point solvents are added, they will evaporate after coating and a transparent coating film will be obtained.

なお、この発明に用いられる着色物質が、上記(2)〜
■)に限定されないことは1うまでもない。たとえば、
塗料中では着色した錯体や複塩、分子化合物等を形成し
ているが、塗装後、経時的に、あるいは加熱や冷却等の
手段により分解、解離等が起こり、それ自身の化学構造
、あるいは含まれる金属イオンの電子配置等が変化して
無色透明となるような化合物であっ”でもよく、金属指
示薬の利用等も可能である。また、着色という概念には
、そのものの存在が6gLHされる程度に白濁している
ような状態のものも含まれる。
Note that the colored substances used in this invention include the above (2) to
It goes without saying that it is not limited to ■). for example,
Colored complexes, double salts, molecular compounds, etc. are formed in paints, but after painting, decomposition and dissociation occur over time or by means of heating, cooling, etc. It may be a compound that becomes colorless and transparent due to a change in the electronic configuration of the metal ion, and it is also possible to use a metal indicator.Also, the concept of coloration includes the degree to which the presence of the substance causes 6gLH. This includes those that are cloudy.

上記着色物質の添加量については、特に限定はされない
が、塗料焼付は後も塗膜中に残存するような着色物質(
たとえば、上記(2)や(aなど)の場合は、塗装時に
膜厚管理ができる程度の最小限の添加量に留めておくこ
吉が好ましい、 塗料組成物に含まれる塗膜形成主要素(樹脂成分)およ
び溶剤等は、特に限定はされず、あらゆるタイプのもの
を使用できる。たとえば、熱硬化型、熱可塑型、光硬化
型、酸化硬化型の樹脂等を塗膜形成主要素とし、必要に
応じて各種添加剤および/または溶剤が添加されたもの
が挙げられ、その用途、使用方法等に応じて、有機溶剤
型、水分散型、水溶液型、ハイソリッド型、粉体型等の
任意の形態をとりうるちのを対象としている。また、こ
の発明にかかる塗料組成物は、金属、プラスチック、紙
、木材等のあらゆる素材からなる被塗物に使用できる。
There are no particular limitations on the amount of the above-mentioned coloring substances added, but coloring substances that remain in the paint film even after the paint is baked (
For example, in the case of (2) and (a) above, it is preferable to keep the addition amount to a minimum enough to control the film thickness during coating. The resin component) and the solvent are not particularly limited, and any type can be used. For example, there are coatings in which thermosetting, thermoplastic, photocuring, or oxidation-curing resins are the main elements for forming coatings, and various additives and/or solvents are added as necessary. , which can take any form such as organic solvent type, water dispersion type, aqueous solution type, high solid type, powder type, etc., depending on the method of use. Furthermore, the coating composition according to the present invention can be used on objects to be coated made of any materials such as metal, plastic, paper, and wood.

つぎに、さらに詳しい実施例につい”で、比較例と併せ
て説明する。
Next, more detailed examples will be explained in "Examples" together with comparative examples.

一実施例および比較例−一 ■ 蓋L口色邊楕) 実施例の塗料組成物には所定量(第1表参照)の下記0
1〜C3のいずれかを添加し、比較例には添加しないよ
うにした。
Example and Comparative Example - 1 Lid L Mouth color Oval) The coating composition of the example was coated with the following 0 in a predetermined amount (see Table 1).
Any one of No. 1 to C3 was added, and no addition was made to the comparative example.

C1:N−ニトロソ−N−メチルウレタン(半井化学薬
品■製、特級) C2:カルミン酸(同上H製、特級) C3:ベンタメトキシレフド (東京化成工業■製、特級) ■ 皇料皿實d廟以週監 下記P1あるいはP2の市販塗料を用いて、以下のよう
にそれぞれを網製した。
C1: N-Nitroso-N-methylurethane (manufactured by Hanui Chemical ■, special grade) C2: Carminic acid (manufactured by H, same as above, special grade) C3: Bentamethoxyrefed (manufactured by Tokyo Kasei Kogyo ■, special grade) ■ Koryo Sarajitsu Using commercially available paints P1 or P2 below, each was made into a net as follows.

Pl:エポキシ樹脂系塗料 (大揺化学工業■製ファスタイト14ON)*専用シン
ナーにより希釈し、フオードカ・ノブ#4で10〜13
秒になるように粘度調整を行った。その後、第1表に示
した着色剤を添加し、よく攪拌して塗料組成物とした。
Pl: Epoxy resin paint (Fastite 14ON manufactured by Daiyo Kagaku Kogyo ■) * Diluted with special thinner, 10 to 13
The viscosity was adjusted so that it was within seconds. Thereafter, the coloring agents shown in Table 1 were added and thoroughly stirred to obtain a coating composition.

P2:有機シリケート系塗料 (日本合成ゴム■製グラスカ90−Aおよび−B)*2
液型塗料であるため、グラス力90−Aとグラス力90
−Bを3:1の割合で混合し、4時間放置した。その後
、第1表に示した着色剤を添加し、よ(攪拌して塗料組
成物とした。ただし、着色剤が上記C3(ベンクメトキ
シレ・ノド)の場合、C3添加後、塩酸を加えてpl(
3に調整した。
P2: Organic silicate paint (Glaska 90-A and -B manufactured by Japan Synthetic Rubber) *2
Because it is a liquid paint, the glass force is 90-A and the glass force is 90
-B was mixed at a ratio of 3:1 and left for 4 hours. Thereafter, the colorant shown in Table 1 was added and stirred to form a coating composition. However, if the colorant is the above C3 (benchmethoxylenod), after adding C3, add hydrochloric acid. pl(
Adjusted to 3.

■ 1装基板 鉄板(縦横300+m、厚さ2關)に銅メツキをし、さ
らにその上にニッケルメッキを施したものを、塗装基板
とした。
■ A coated board was made by plating a steel plate (300+ m in length and width, 2 m in thickness) with copper, and then plating it with nickel.

■ 1装 調製済みの上記塗料を、スプレーガンを用い、膜厚10
μmとなるように上記基板に塗布した。このとき、重量
法により塗料の塗着重量を測定して、塗装膜厚をチエツ
クしながら塗装を行った。
■ Use a spray gun to apply one coat of the above paint to a film thickness of 10
It was coated on the above substrate so that the thickness was .mu.m. At this time, the applied weight of the paint was measured by a gravimetric method, and the coating was performed while checking the coating film thickness.

■ 血仕り 遠赤外線炉を用い、塗料が上記Pi(ファスタイト)の
場合は150℃×20分間、P2 (グラス力)の場合
は180℃×20分間、それぞれ焼(NJけを行った。
(2) Baking (NJ firing) was performed using a far-infrared furnace at 150°C for 20 minutes when the paint was Pi (Fastite), and at 180°C for 20 minutes when the paint was P2 (Glass Power).

塗装板(縦横300m)を、縦横60mの同じ大きさの
正方形25区画に分割し、各区画の膜厚を電磁式膜厚計
(■サンコラ電子研究所製5M−100)で測定し、平
均値と標準偏差を算出した。
A painted board (300 m in length and width) was divided into 25 square sections of the same size, 60 m in length and width, and the film thickness of each section was measured with an electromagnetic film thickness meter (5M-100 manufactured by Sancora Electronic Research Institute), and the average value was determined. and the standard deviation was calculated.

(イ)   l穴「イ寸二紀す丁1コ4しりtし且会コ
υ(コ芒l基板に所定重量の塗料組成物を塗装した後、
目視により塗膜の着色状態を評価した。
(a) After applying a predetermined weight of the paint composition to the substrate,
The coloring state of the coating film was evaluated visually.

(つ)    1食L(t3リニt(二qλ2zしル〈
伏ia所定条件で焼付けを行2った後の塗膜の着色状態
(tsu) 1 meal L (t3 linit (2qλ2zshiru)
Colored state of the paint film after baking under specified conditions.

を、目視に、より評(而した。was visually evaluated.

以上の結果を、同じく第1表に示す。The above results are also shown in Table 1.

第1表にみるように、01〜c3の着色剤を添加した実
施例の塗料組成物では、塗装時点での目視による膜厚管
理が可能であった。その結果、ムラのない均一な塗装を
行うことができ、実際に焼付けを行った後の膜厚測定結
果からも、膜厚のバラツキが小さく、均一な塗膜が得ら
れたことが確認できた。
As shown in Table 1, in the coating compositions of Examples in which colorants 01 to C3 were added, it was possible to control the film thickness by visual observation at the time of coating. As a result, it was possible to apply a uniform coating without any unevenness, and the film thickness measurement results after actual baking confirmed that a uniform coating film was obtained with little variation in film thickness. .

〔発明の効果〕〔Effect of the invention〕

この発明にかかる塗料組成物は、透明な塗膜を形成する
ものでありながら、塗装時には有色であることを特徴と
しているため、塗膜の膜厚を管理しながら塗装を行うこ
とができ、より均一な透明塗膜が形成されるようになる
。したがって、この塗料組成物を用いて、たとえば、照
明器具部品等の保護コートを行うと、それらの製品の特
性を損なうことなく、容易に均一な透明保護膜を形成す
ることが可能となる。
The coating composition according to the present invention is characterized in that although it forms a transparent coating film, it is colored at the time of coating, so coating can be performed while controlling the thickness of the coating film, making it more A uniform transparent coating will be formed. Therefore, when this coating composition is used to protect lighting equipment parts, for example, it becomes possible to easily form a uniform transparent protective film without impairing the properties of those products.

代理人 弁理士  松 本 武 彦Agent: Patent Attorney Takehiko Matsumoto

Claims (1)

【特許請求の範囲】[Claims] 1 透明な塗膜を形成する塗料組成物であって、塗装時
には着色している着色物質を含み、同着色物質が塗装の
のちに無色に変わるか塗膜中から消失することにより、
透明な塗膜を形成するようになっていることを特徴とす
る塗料組成物。
1. A coating composition that forms a transparent coating film, which contains a colored substance that is colored at the time of coating, and that the colored substance turns colorless or disappears from the coating film after coating.
A coating composition characterized in that it forms a transparent coating film.
JP10188188A 1988-04-25 1988-04-25 Coating composition Pending JPH01272672A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10188188A JPH01272672A (en) 1988-04-25 1988-04-25 Coating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10188188A JPH01272672A (en) 1988-04-25 1988-04-25 Coating composition

Publications (1)

Publication Number Publication Date
JPH01272672A true JPH01272672A (en) 1989-10-31

Family

ID=14312286

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10188188A Pending JPH01272672A (en) 1988-04-25 1988-04-25 Coating composition

Country Status (1)

Country Link
JP (1) JPH01272672A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001252615A (en) * 2000-03-10 2001-09-18 Nippon Soda Co Ltd Coating method and structure coated by using the same
JP2015057282A (en) * 2014-10-29 2015-03-26 ベック株式会社 Coating film formation method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001252615A (en) * 2000-03-10 2001-09-18 Nippon Soda Co Ltd Coating method and structure coated by using the same
JP2015057282A (en) * 2014-10-29 2015-03-26 ベック株式会社 Coating film formation method

Similar Documents

Publication Publication Date Title
CN109666376B (en) Stimulus-responsive color-changing functional coating and preparation method and application thereof
JP6323932B2 (en) Coating composition and coating film forming method
JPH01272672A (en) Coating composition
Ma et al. Preparation of reversible thermochromic building coatings and their properties
ITTO960897A1 (en) PROCEDURE FOR FORMING A PROTECTIVE LAYER ON A REFLECTIVE METALLIC LAYER WITHOUT COPPER.
CN111892860B (en) Energy-storage luminous powder coating and production construction method
JPH0525899A (en) Coating with transparent coating material
CN107011702A (en) A kind of trbasic zinc phosphate wraps up the synthetic method of heat resistant type ferric oxide yellow pigment
MXPA04011694A (en) Method for determining cure in a polycarboxylic acid bindered material.
CN112795295A (en) Temperature-sensitive color-changing floor and preparation method thereof
CN211606911U (en) Electronic product
KR0135330B1 (en) Transparent cracking paint compositons
CN106916482A (en) A kind of heat resistant type ferric oxide yellow pigment and preparation method thereof
CN113308161A (en) Composition for matte antibacterial and antiviral coating, matte antibacterial and antiviral coating prepared from composition and application of composition
JP6037549B2 (en) Coating material
CN102515876B (en) Resin acid titanium-iron-bismuth system yellow-series electro-optic water and preparation method thereof
Pataki-Hundt Characteristics of natural and synthetic adhesives
JPS62132975A (en) Paint and method for inspecting application of paint
KR20010089978A (en) Coating Material Comprising Aqueous Silicate Solution and a Coating Method Using The Same
JPS61242941A (en) Finish paint for inorganic construction material
JP4098608B2 (en) Designed coating film and building material
JPS6010794B2 (en) Manufacturing method of heat-resistant coating layer
JP4999607B2 (en) Repair agent for lacquer coating
JP2003043161A (en) Clear coating inspection method of external facing building member
JP4254096B2 (en) Method for forming transparent inorganic coating film