JPH01272672A - Coating composition - Google Patents
Coating compositionInfo
- 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
Links
- 239000008199 coating composition Substances 0.000 title claims abstract description 20
- 238000000576 coating method Methods 0.000 claims abstract description 38
- 239000011248 coating agent Substances 0.000 claims abstract description 36
- 239000000126 substance Substances 0.000 claims abstract description 14
- 238000004040 coloring Methods 0.000 abstract description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 6
- 239000002696 acid base indicator Substances 0.000 abstract description 3
- 239000012445 acidic reagent Substances 0.000 abstract description 3
- 239000002184 metal Substances 0.000 abstract description 3
- 229910052751 metal Inorganic materials 0.000 abstract description 3
- CMYZTJCWFRFRIW-UHFFFAOYSA-N 1-bromo-4-(4-methoxyphenyl)benzene Chemical compound C1=CC(OC)=CC=C1C1=CC=C(Br)C=C1 CMYZTJCWFRFRIW-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000011253 protective coating Substances 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 description 23
- 230000002378 acidificating effect Effects 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 238000010422 painting Methods 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- CAUBWLYZCDDYEF-UHFFFAOYSA-N N-Nitroso-N-methylurethane Chemical compound CCOC(=O)N(C)N=O CAUBWLYZCDDYEF-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- DGQLVPJVXFOQEV-NGOCYOHBSA-N carminic acid Chemical compound OC1=C2C(=O)C=3C(C)=C(C(O)=O)C(O)=CC=3C(=O)C2=C(O)C(O)=C1[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DGQLVPJVXFOQEV-NGOCYOHBSA-N 0.000 description 2
- 229940114118 carminic acid Drugs 0.000 description 2
- 235000012730 carminic acid Nutrition 0.000 description 2
- 239000004106 carminic acid Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- WOAHJDHKFWSLKE-UHFFFAOYSA-N 1,2-benzoquinone Chemical compound O=C1C=CC=CC1=O WOAHJDHKFWSLKE-UHFFFAOYSA-N 0.000 description 1
- KETQAJRQOHHATG-UHFFFAOYSA-N 1,2-naphthoquinone Chemical compound C1=CC=C2C(=O)C(=O)C=CC2=C1 KETQAJRQOHHATG-UHFFFAOYSA-N 0.000 description 1
- 229940105324 1,2-naphthoquinone Drugs 0.000 description 1
- CPBJMKMKNCRKQB-UHFFFAOYSA-N 3,3-bis(4-hydroxy-3-methylphenyl)-2-benzofuran-1-one Chemical compound C1=C(O)C(C)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C=C(C)C(O)=CC=2)=C1 CPBJMKMKNCRKQB-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- LDKDGDIWEUUXSH-UHFFFAOYSA-N Thymophthalein Chemical compound C1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C(=CC(O)=C(C(C)C)C=2)C)=C1C LDKDGDIWEUUXSH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- NCYVXEGFNDZQCU-UHFFFAOYSA-N nikethamide Chemical compound CCN(CC)C(=O)C1=CC=CN=C1 NCYVXEGFNDZQCU-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- GLQWRXYOTXRDNH-UHFFFAOYSA-N thiophen-2-amine Chemical compound NC1=CC=CS1 GLQWRXYOTXRDNH-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
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、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.
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.
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.
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.
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. .
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)
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.
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)
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 |
-
1988
- 1988-04-25 JP JP10188188A patent/JPH01272672A/en active Pending
Cited By (2)
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 |
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