JPH01289875A - Coating composition - Google Patents

Coating composition

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Publication number
JPH01289875A
JPH01289875A JP11844088A JP11844088A JPH01289875A JP H01289875 A JPH01289875 A JP H01289875A JP 11844088 A JP11844088 A JP 11844088A JP 11844088 A JP11844088 A JP 11844088A JP H01289875 A JPH01289875 A JP H01289875A
Authority
JP
Japan
Prior art keywords
water
dew condensation
condensation
parts
coating film
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
JP11844088A
Other languages
Japanese (ja)
Inventor
Masahiro Asami
浅見 正廣
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.)
Daicel Corp
Original Assignee
Daicel Chemical Industries 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 Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Priority to JP11844088A priority Critical patent/JPH01289875A/en
Publication of JPH01289875A publication Critical patent/JPH01289875A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a coating composition which can absorb moisture and water formed by condensation in good efficiency and can prevent dew condensation from occurring on the surface of a coating film under conditions of dew condensation by mixing a specified synthetic resin emulsion with a water-soluble complex compound and a porous inorganic substance. CONSTITUTION:A porous inorganic substance (e.g., zeolite or silica gel) is added to a mixture formed by dispersing a water-soluble complex compound comprising a bivalent or higher valent metal salt and a volatile complexing agent [e.g., one formed by adding ZnO and (NH4)2CO3 in water and adding ammonia water thereto so that the pH is 7 or above and agitating the mixture] and a synthetic emulsion comprising 0.1-30wt.% ethylenically unsaturated carboxylic acid [e.g., (meth)acrylic acid or maleic acid (anhydride)] and 99.9-70wt.% monomer copolymerizable therewith (e.g., methyl (meth)acrylate). A coating composition which can absorb moisture or water formed by condensation in good efficiency under conditions of dew condensation and can prevent dew condensation from occurring on the surface of a coating film can be obtained.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は建築物の壁面、天井、配管などの結露の生じや
すい箇所の結露を防止する塗料組成物に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a coating composition that prevents dew condensation on areas where condensation is likely to occur, such as walls, ceilings, and piping of buildings.

(従来の技術) 従来より結露を防止する方法として、種々の方法が提案
されているが、手軽に処置できる方法として、特公昭6
2−15108号公報に開示されているような塗料、即
ち合成樹脂エマルジョンの塗膜形成要素中にゼオライト
、珪藻土、シリカゲル等多孔質の無機物材料を充填材と
した塗料を塗装し、その塗膜中に湿気や結露水を含水さ
せることにより、水滴状の結露を防止する方法があった
(Prior art) Various methods have been proposed to prevent dew condensation.
A paint as disclosed in Publication No. 2-15108, that is, a paint containing a porous inorganic material such as zeolite, diatomaceous earth, or silica gel as a filler is applied to the film-forming element of a synthetic resin emulsion. There is a method to prevent condensation in the form of droplets by adding moisture or condensation water to the surface.

(発明が解決しようとする課題) しかしながら、合成樹脂エマルジョンは本質的に親水性
であるため、長時間塗膜中に多量の結露水を含水したり
、あるいは浴室等で水がかかるような場合には、親水性
成分部分が流失し、多孔質の充填材を結合する力、即ち
バインダーとしての性能が弱まり、塗膜が損失してしま
うという問題があった。
(Problem to be Solved by the Invention) However, since synthetic resin emulsions are essentially hydrophilic, they may contain a large amount of condensed water in the coating film for a long period of time, or may be exposed to water in the bathroom etc. However, there was a problem in that the hydrophilic component part was washed away, the ability to bind the porous filler, that is, the performance as a binder was weakened, and the coating film was lost.

本発明の目的は、長時間塗膜中に多量の結露水を含水し
たり、水が塗面にかかっても塗膜の損失がなく、結露を
防止する塗料組成物を提供することにある。
An object of the present invention is to provide a coating composition that prevents dew condensation and does not cause loss of the coating film even if a large amount of dew water is contained in the coating film for a long period of time or water is splashed onto the coated surface.

(課題を解決するための手段) 塗料の可使時間が長く耐水性の良好な塗膜を与える合成
樹脂エマルジョンについて検討した結果、エチレン性不
飽和カルボン酸0:1〜30重量%と、エチレン性不飽
和カルボン酸と共重合可能な単量体99.9〜70重量
%とからなる合成樹脂エマルジョンと、二価以上の金属
塩と揮発性錯化剤とからなる水溶性錯化物との混合物が
長時間安定でかつ、その塗膜の耐水性が良いことを知り
、上記混合物に多孔質無機物を配合することにより耐水
性の良い結露防止用塗料が得られることを見出だし、本
発明を完成しな。
(Means for solving the problem) As a result of studying synthetic resin emulsions that provide a paint film with a long pot life and good water resistance, we found that 0:1 to 30% by weight of ethylenically unsaturated carboxylic acid and ethylenic A mixture of a synthetic resin emulsion consisting of an unsaturated carboxylic acid and 99.9 to 70% by weight of a copolymerizable monomer, and a water-soluble complex consisting of a divalent or higher valent metal salt and a volatile complexing agent. After learning that the paint film was stable for a long time and had good water resistance, he discovered that by adding a porous inorganic substance to the above mixture, a water-resistant anti-condensation paint could be obtained, and thus completed the present invention. Na.

本発明で使用される、エチレン性不飽和カルボン酸とし
ては、アクリル酸、メタクリル酸、イタコン酸、クロト
ン酸、マレイン酸、無水マレイン酸等のエチレン性不飽
和カルボン酸等が含まれる。
The ethylenically unsaturated carboxylic acids used in the present invention include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, maleic acid, and maleic anhydride.

エチレン性不飽和カルボン酸の使用量としては、0.1
〜30重量%で、好ましくは1.5〜5重量%である。
The amount of ethylenically unsaturated carboxylic acid used is 0.1
-30% by weight, preferably 1.5-5% by weight.

0,1重量%未満の場合は水溶性錯化物との架橋が不十
分であり、耐水性、造膜性が悪くなる。
If it is less than 0.1% by weight, crosslinking with the water-soluble complex will be insufficient, resulting in poor water resistance and film-forming properties.

また、30重量%を越える場合は耐水性が落ちてきて実
用上使用に耐えない。
Moreover, if it exceeds 30% by weight, the water resistance decreases and it is not suitable for practical use.

本発明で使用される、エチレン性不飽和カルボン酸と共
重合可能な単量体としては、アクリル酸メチル、アクリ
ル酸エチル、アクリル酸ブチル、アクリル酸2−エチル
ヘキシル、メタクリル酸メチル、メタクリル酸ブチル、
メタクリル酸2−エチルヘキシル、メタクリル酸ステア
リル等のエチレン性不飽和カルボン酸のアルキルエステ
ル、メタクリル酸2−ヒドロキシエチル等のエチレン性
不飽和カルボン酸のヒドロキシアルキルエステル、メタ
クリル酸グリシジル等のエチレン性不飽和カルボン酸の
グリシジルエステル、アクリルアミド、N−メチロール
アクリルアミド、N−ブチロ−ルアクリルアミド等のエ
チレン性不飽和カルボン酸のアミド化合物、酢酸ビニル
等のビニルエステル、酢酸アリル等のアリルエステル、
ビニルメチルエーテル等のビニルエーテル、塩化ビニリ
デン、塩化ビニル、アクリロニトリル、エチレン等が挙
げられる。
Monomers copolymerizable with ethylenically unsaturated carboxylic acids used in the present invention include methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, butyl methacrylate,
Alkyl esters of ethylenically unsaturated carboxylic acids such as 2-ethylhexyl methacrylate and stearyl methacrylate, hydroxyalkyl esters of ethylenically unsaturated carboxylic acids such as 2-hydroxyethyl methacrylate, and ethylenically unsaturated carboxylic acids such as glycidyl methacrylate. Glycidyl esters of acids, amide compounds of ethylenically unsaturated carboxylic acids such as acrylamide, N-methylolacrylamide, N-butyrolacrylamide, vinyl esters such as vinyl acetate, allyl esters such as allyl acetate,
Examples include vinyl ethers such as vinyl methyl ether, vinylidene chloride, vinyl chloride, acrylonitrile, and ethylene.

本発明で使用される合成樹脂エマルジョンはエチレン性
不飽和カルボン酸とエチレン性不飽和カルボン酸と共重
合可能な単量体を用いて、公知の乳化重合方法によって
製造できる。なおエマルジョン中の樹脂濃度は通常20
〜65%の範囲で使用される。
The synthetic resin emulsion used in the present invention can be produced by a known emulsion polymerization method using an ethylenically unsaturated carboxylic acid and a monomer copolymerizable with the ethylenically unsaturated carboxylic acid. The resin concentration in the emulsion is usually 20
It is used in the range of ~65%.

本発明で使用される二価以上の金属塩と揮発性アミンと
からなる水溶性錯化物とは、亜鉛、ニッケル、銅、チタ
ン、モリブデン、コバルト、鉄等の炭酸塩、リン酸塩、
亜リン酸塩等の無機物の塩、あるいはフェノールカルボ
ン酸、ソルビン酸、フミン酸等の有機物の塩と、アンモ
ニアあるいはトリメチルアミン、ジエチルアミン、トリ
エチルアミン、トリエタノールアミン、モルホリン等の
揮発性アミン等の揮発性錯1ヒ剤との水溶性錯化物であ
る。特に限定されるものではないが、水溶性錯化物の製
造方法の一例を挙げると、水に酸化亜鉛、炭酸アンモニ
ウムを分散させ、このものにPHが7以上になるように
アンモニア水を加えて、撹拌すれば水溶性開化物の水溶
液が得られる。上記水溶性錯化物については、特開昭4
9−96033号公報、特開昭62−257972号公
報にも開示されている。
The water-soluble complexes consisting of divalent or higher metal salts and volatile amines used in the present invention include carbonates, phosphates, etc. of zinc, nickel, copper, titanium, molybdenum, cobalt, iron, etc.
Salts of inorganic substances such as phosphites, or salts of organic substances such as phenol carboxylic acids, sorbic acids, and humic acids, and volatile complexes such as ammonia or volatile amines such as trimethylamine, diethylamine, triethylamine, triethanolamine, and morpholine. It is a water-soluble complex with 1 drug. Although not particularly limited, an example of a method for producing a water-soluble complex is to disperse zinc oxide and ammonium carbonate in water, and add aqueous ammonia to this so that the pH becomes 7 or more. By stirring, an aqueous solution of the water-soluble compound can be obtained. Regarding the water-soluble complexes mentioned above, JP-A No. 4
It is also disclosed in Japanese Patent Application Laid-open No. 9-96033 and Japanese Patent Application Laid-Open No. 62-257972.

上記水溶性錯化物は合成樹脂エマルジョンに含まれるエ
チレン性不飽和カルボン酸に由来するカルボキシル基1
モル当り、0.2〜1.5モルの割合で使用するのが好
ましい、水溶性錯化物の割合が0.2モル未満の場合は
水溶性錯化物との架橋の程度が不十分であり、耐水性が
劣り、1.5モルを越える場合は必要以上の親水性成分
が塗膜に存在し、その結果耐水性が落ちてきて実用上使
用に耐えないこともある。
The above-mentioned water-soluble complex has a carboxyl group derived from ethylenically unsaturated carboxylic acid contained in the synthetic resin emulsion.
It is preferable to use the water-soluble complex in a proportion of 0.2 to 1.5 moles per mole; if the proportion of the water-soluble complex is less than 0.2 mole, the degree of crosslinking with the water-soluble complex is insufficient; Water resistance is poor, and if the amount exceeds 1.5 mol, more hydrophilic components than necessary will be present in the coating film, resulting in decreased water resistance and may not be suitable for practical use.

本発明で使用する多孔質無機物としては、ゼオライト、
珪藻土、シリカゲル、パーライト等であり、合成樹脂エ
マルジョンの固形分100重量部に対して、多孔質無機
物を100〜600重量部、好ましくは150〜400
重量部配合すれば配合、多孔質熱ti物の量が100重
量部未満では、相対的に合成樹脂エマルジョンの量が多
くなるため、多孔質熱ti物の表面の大部分が被覆され
てしまい、吸水能力が低下し、その結果結露防止性が悪
くなる。また、600重量部を越えると、相対的に合成
樹脂エマルジョンの量が少なくなり、結合力に乏しく、
塗膜の耐水性が悪くなる。
Porous inorganic substances used in the present invention include zeolite,
diatomaceous earth, silica gel, perlite, etc., and the porous inorganic material is 100 to 600 parts by weight, preferably 150 to 400 parts by weight, per 100 parts by weight of the solid content of the synthetic resin emulsion.
If the amount of porous hot Ti material is less than 100 parts by weight, the amount of synthetic resin emulsion will be relatively large, and most of the surface of the porous hot Ti material will be covered. Water absorption capacity decreases, resulting in poor dew condensation prevention. Moreover, if it exceeds 600 parts by weight, the amount of synthetic resin emulsion will be relatively small, and the binding strength will be poor.
The water resistance of the paint film deteriorates.

本発明の塗料組成物は本発明の目的を損なわない範囲で
一般的な水性塗料に使用する各種添加剤を配合すること
ができる。これらの添加剤としては、分散剤、消泡剤、
湿潤剤、乳化剤、帯電防止剤、造膜助剤、凍結安定剤、
可逆剤、増粘剤、防腐剤、顔料、染料、骨材等が挙げら
れる。
The coating composition of the present invention may contain various additives used in general water-based coatings as long as the purpose of the present invention is not impaired. These additives include dispersants, antifoaming agents,
Wetting agents, emulsifiers, antistatic agents, coating aids, freeze stabilizers,
Examples include reversible agents, thickeners, preservatives, pigments, dyes, and aggregates.

(発明の効果) 本発明の塗料組成物は、含有する多孔質無機物により、
結露発生条件下において、湿気または結露水を効率よく
吸収でき、塗膜表面での結露の発生を防ぐことができる
。さらに、合成樹脂エマルジョン中に含まれるカルボン
キシル基と二価以上の金属が強固なイオン結合を生じ、
耐水性の優れた塗膜を形成し、そのためこの塗膜は多量
の結露水を吸収したり、また浴室等に塗装され水が塗面
にかかったりしても、塗膜が損傷しない耐水性を有して
いる。また、本発明の塗料組成物は水性であるため火災
の危険が少なく、有機溶剤の多量の蒸散による大気の汚
染が無い。
(Effects of the invention) The coating composition of the present invention has
Under conditions where condensation occurs, moisture or condensed water can be efficiently absorbed, and dew condensation can be prevented from occurring on the coating surface. Furthermore, the carboxyl group contained in the synthetic resin emulsion and the divalent or higher valent metal form a strong ionic bond,
It forms a coating film with excellent water resistance, so even if this coating film absorbs a large amount of condensed water, or if it is painted in a bathroom or other area and gets wet with water, the coating film will not be damaged. have. Furthermore, since the coating composition of the present invention is water-based, there is little risk of fire, and there is no air pollution due to transpiration of large amounts of organic solvents.

(実施例) 次に実施例にて本発明をさらに説明する。なお、実施例
、比較例、合成例において部及び%は、各々重量部及び
重量%を示す。
(Example) Next, the present invention will be further explained with reference to Examples. In Examples, Comparative Examples, and Synthesis Examples, parts and % indicate parts by weight and % by weight, respectively.

合成例1 撹拌機、環流冷却器、滴下装置及び温度計のついた重合
缶に、水35.6部、及びノニルフェニルエーテルポリ
オキシエチレン硫酸ナトリウム2,8部を仕込み、75
℃まで昇温する。窒素気流中でスチレン19.8部、ア
クリル酸2−エチルヘキシル32.2部、メタクリル酸
メチル4゜7部及びアクリル酸2.3部の混合モノマー
と5%過硫酸アンモニウム水溶液5部及び5%亜硫酸水
素ナトリウム水溶液5部を各々5時間かけて滴下する。
Synthesis Example 1 35.6 parts of water and 2.8 parts of sodium nonylphenyl ether polyoxyethylene sulfate were charged into a polymerization vessel equipped with a stirrer, a reflux condenser, a dropping device, and a thermometer.
Raise the temperature to ℃. In a nitrogen stream, a monomer mixture of 19.8 parts of styrene, 32.2 parts of 2-ethylhexyl acrylate, 4.7 parts of methyl methacrylate, and 2.3 parts of acrylic acid, 5 parts of a 5% ammonium persulfate aqueous solution, and 5% hydrogen sulfite. 5 parts of aqueous sodium solution are added dropwise over 5 hours each.

その後75℃で重合反応を2時間行う、室温まで冷却し
た後、25%アンモニア水を用いて、PH8まで調整す
る。
Thereafter, a polymerization reaction is carried out at 75° C. for 2 hours, and after cooling to room temperature, the pH is adjusted to 8 using 25% aqueous ammonia.

かくして濃度49.6%、粘度80cps  (30°
C)のエマルジョンが得られた。
Thus, the concentration is 49.6% and the viscosity is 80 cps (30°
An emulsion C) was obtained.

合成例2 水16部にアルキルエーテルリン酸エステルナトリウム
0.8部とアルキルフェニールエーテルポリオキシエチ
レン1.2部を溶解し、このものにメタクリル酸メチル
16部、アクリル酸エチル22部及びアクリル酸1.7
部を加えて十分に分散させる。この分散液の10%と水
31部、アルキルエーテルリン酸エステルナトリウム0
.8部及びアルキルフェニルエーテルポリオキシエチレ
ン1゜2部を撹拌機、環流冷却器、滴下装置及び温度計
のついた重合缶に仕込み、窒素気流中で80℃まで昇温
する。5%過硫酸アンモニウム水溶液0.5部及び5%
亜硫酸水素ナトリウム0.5部を加えて、1時間重合を
行う0次いで先に調整した分散液90%と5%過硫酸ア
ンモニウム水溶液4.5部及び5%亜硫酸水素ナトリウ
ム水溶液4.5部を各々3時間かけて滴下する。その後
85℃まで昇温し、重合反応を3時間行なう、室温まで
冷却した後、25%アンモニア水を用いて得られたエマ
ルジョンのPHを8.5に調整する。この時のエマルジ
ョンの濃度は40.1%、粘度は460cps (30
℃)であった。
Synthesis Example 2 0.8 parts of sodium alkyl ether phosphate and 1.2 parts of alkyl phenyl ether polyoxyethylene were dissolved in 16 parts of water, and 16 parts of methyl methacrylate, 22 parts of ethyl acrylate, and 1 part of acrylic acid were dissolved in this solution. .7
of water and disperse thoroughly. 10% of this dispersion, 31 parts of water, 0 sodium alkyl ether phosphate
.. 8 parts and 1.2 parts of alkylphenyl ether polyoxyethylene are charged into a polymerization vessel equipped with a stirrer, a reflux condenser, a dropping device and a thermometer, and the temperature is raised to 80°C in a nitrogen stream. 0.5 parts of 5% ammonium persulfate aqueous solution and 5%
Add 0.5 parts of sodium bisulfite and conduct polymerization for 1 hour. Next, add 3 parts each of the 90% dispersion prepared above, 4.5 parts of 5% ammonium persulfate aqueous solution, and 4.5 parts of 5% sodium bisulfite aqueous solution. Drip over time. Thereafter, the temperature was raised to 85° C. and a polymerization reaction was carried out for 3 hours. After cooling to room temperature, the pH of the obtained emulsion was adjusted to 8.5 using 25% aqueous ammonia. The concentration of the emulsion at this time was 40.1%, and the viscosity was 460 cps (30
℃).

実施例1 合成例1のエマルジョン104部と20%炭酸アンモニ
ウム水溶液16部、酢酸ブチルセロソルブ6部、分散剤
1部、湿潤剤1部、酸化チタン10部、珪藻土120部
、5%ヒドロキシエチルセルロース水溶液6部、消泡剤
1部をデイスパーミルを用いて十分に混合する。この塗
料を結露発生のたびたび見られた浴室の天井面にローラ
バゲで塗装して、結露発生の状態を1fJ月間観察した
が結露の発生は全くみられず、また塗装表面の亀裂、ひ
び割れ等の異状も全くみられなかった。また、7511
1X150nnの鉄板に上記塗料をローラノくケにて厚
さ0゜5nnになるように塗装した後、20°C165
%RHの雰囲気で7日間乾燥した。この試料につ(1て
、塗面状態観察及び耐水性、吸水性について観察した。
Example 1 104 parts of the emulsion of Synthesis Example 1, 16 parts of 20% ammonium carbonate aqueous solution, 6 parts of butyl cellosolve acetate, 1 part of dispersant, 1 part of wetting agent, 10 parts of titanium oxide, 120 parts of diatomaceous earth, 6 parts of 5% hydroxyethylcellulose aqueous solution , 1 part of antifoaming agent is thoroughly mixed using a disper mill. This paint was applied to the ceiling of the bathroom where dew condensation was frequently observed using a roller bagger, and the state of dew condensation was observed for 1fJ months, but no condensation was observed, and there were no abnormalities such as cracks or cracks on the painted surface. was not seen at all. Also, 7511
After applying the above paint to a 1x150nn iron plate with a roller to a thickness of 0°5nn, heat it at 20°C165.
%RH atmosphere for 7 days. Regarding this sample (1), the condition of the painted surface and water resistance and water absorption were observed.

その結果を表2に示す。The results are shown in Table 2.

〈実施例2〜4) 表1に示す配合比に従って実施例1と同様な方法で塗料
を製造し、実施例1と同様の方法で試験した。その結果
を表2に示す。
<Examples 2 to 4> Paints were manufactured in the same manner as in Example 1 according to the compounding ratios shown in Table 1, and tested in the same manner as in Example 1. The results are shown in Table 2.

(比較例1〜2) 表1に示す配合比に従って実施例1と同様な方法で塗料
を製造し、実施例1と同様の方法で試験した。その結果
を表2に示す。
(Comparative Examples 1 and 2) Paints were manufactured in the same manner as in Example 1 according to the compounding ratios shown in Table 1, and tested in the same manner as in Example 1. The results are shown in Table 2.

(評価方法) 1、浴室での結露の発生 結露の発生がたびたび見られた浴室の天井面にローラバ
ゲで塗装して結露の発生状況を1力月間観察する。結露
の発生が見られなかったものはO1結露の発生が見られ
たものは×で示す。
(Evaluation method) 1. Occurrence of dew condensation in the bathroom Paint the ceiling of the bathroom where condensation was frequently observed with a roller bag and observe the occurrence of condensation for one month. Those in which no dew condensation was observed and those in which O1 condensation was observed are indicated by an x.

2、塗面の状態 塗料乾燥後の塗面の状態を肉眼で観察した。亀裂が全く
見られなかったものは◎、亀裂が少し見られたものを○
、亀裂が全面に見られたものを×で示す。
2. Condition of the painted surface The condition of the painted surface after the paint had dried was observed with the naked eye. Items with no cracks at all are ◎, items with some cracks are ○
, Those in which cracks were observed over the entire surface are indicated by an x.

3、耐水性(20℃) 試験片を7日間20℃の水に浸漬し、塗膜の状態を肉眼
で観察した。全く異常が見られなかったものは◎、塗膜
が軟化しただけのものを○、塗膜が水中に溶けだしたも
のをXで示す。
3. Water resistance (20°C) The test piece was immersed in water at 20°C for 7 days, and the state of the coating film was observed with the naked eye. A case where no abnormality was observed is indicated by ◎, a case where the coating film was only softened is indicated by ○, and a case where the coating film began to dissolve into water is indicated by X.

4、耐水性(80°C) 試験片を1時間80°Cの水に浸漬し、塗膜の状態を肉
眼で観察した。全く異常が見られなかったものは◎、塗
膜が軟化しただけのものを○、塗膜が水中に溶けだした
ものをXで示す。
4. Water resistance (80°C) The test piece was immersed in water at 80°C for 1 hour, and the condition of the coating film was observed with the naked eye. A case where no abnormality was observed is indicated by ◎, a case where the coating film was only softened is indicated by ○, and a case where the coating film began to dissolve into water is indicated by X.

5.吸水性 試験片を3時間20℃の水に浸漬し1、吸水した水量を
測定し、該塗料をill厚で、1Mに塗布した時に吸水
した水量に換算して評価した。吸水した水量が3009
以上であれば結露防止能力があり、○で示し、吸水した
水量が30(13未満であれば結露防止能力がなく、×
で示す。
5. A water absorption test piece was immersed in water at 20° C. for 3 hours, the amount of water absorbed was measured, and the evaluation was made by converting it into the amount of water absorbed when the paint was applied to an illumination thickness of 1M. The amount of water absorbed is 3009
If it is above, there is dew condensation prevention ability, and it is indicated by ○, and if the amount of water absorbed is less than 30, there is no dew condensation prevention ability, and ×
Indicated by

Claims (1)

【特許請求の範囲】 エチレン性不飽和カルボン酸0.1〜30重量%とエチ
レン性不飽和カルボン酸と共重合可能な単量体99.9
〜70重量%とからなる合成樹脂エマルジョンと、 二価以上の金属塩と揮発性錯化剤とからなる水溶性錯化
物と、 多孔質無機物 とからなる塗料組成物
[Claims] 0.1 to 30% by weight of ethylenically unsaturated carboxylic acid and 99.9% of a monomer copolymerizable with ethylenically unsaturated carboxylic acid.
A coating composition comprising a synthetic resin emulsion comprising ~70% by weight, a water-soluble complex comprising a divalent or higher metal salt and a volatile complexing agent, and a porous inorganic substance.
JP11844088A 1988-05-16 1988-05-16 Coating composition Pending JPH01289875A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11844088A JPH01289875A (en) 1988-05-16 1988-05-16 Coating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11844088A JPH01289875A (en) 1988-05-16 1988-05-16 Coating composition

Publications (1)

Publication Number Publication Date
JPH01289875A true JPH01289875A (en) 1989-11-21

Family

ID=14736691

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11844088A Pending JPH01289875A (en) 1988-05-16 1988-05-16 Coating composition

Country Status (1)

Country Link
JP (1) JPH01289875A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111560204A (en) * 2020-06-15 2020-08-21 李艳艳 Self-repairable polycarbonate surface antifogging coating and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4833257A (en) * 1971-08-30 1973-05-08
JPS5339987A (en) * 1976-09-25 1978-04-12 Yuuhou Shiyoukai Kk Floor polish emulsion composition
JPS54141822A (en) * 1978-04-27 1979-11-05 Toyo Soda Mfg Co Ltd Coating composition
JPS63108085A (en) * 1986-05-02 1988-05-12 Shikoku Kaken Kogyo Co Ltd Covering composition for preventing dew condensation

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4833257A (en) * 1971-08-30 1973-05-08
JPS5339987A (en) * 1976-09-25 1978-04-12 Yuuhou Shiyoukai Kk Floor polish emulsion composition
JPS54141822A (en) * 1978-04-27 1979-11-05 Toyo Soda Mfg Co Ltd Coating composition
JPS63108085A (en) * 1986-05-02 1988-05-12 Shikoku Kaken Kogyo Co Ltd Covering composition for preventing dew condensation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111560204A (en) * 2020-06-15 2020-08-21 李艳艳 Self-repairable polycarbonate surface antifogging coating and preparation method thereof

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