JPS62260870A - Sealer composition for inorganic porous substrate - Google Patents

Sealer composition for inorganic porous substrate

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Publication number
JPS62260870A
JPS62260870A JP10382686A JP10382686A JPS62260870A JP S62260870 A JPS62260870 A JP S62260870A JP 10382686 A JP10382686 A JP 10382686A JP 10382686 A JP10382686 A JP 10382686A JP S62260870 A JPS62260870 A JP S62260870A
Authority
JP
Japan
Prior art keywords
water
monomer
parts
inorganic porous
polymerizable monomer
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
JP10382686A
Other languages
Japanese (ja)
Inventor
Teruo Kikuta
照夫 菊田
Kohei Hori
堀 耕平
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Shokubai Co Ltd
Original Assignee
Nippon Shokubai Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Shokubai Co Ltd filed Critical Nippon Shokubai Co Ltd
Priority to JP10382686A priority Critical patent/JPS62260870A/en
Publication of JPS62260870A publication Critical patent/JPS62260870A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide the title compsn. which has excellent safety and gives a coating film having excellent reinforcibility, durability, etc., containing a water-soluble resin obtd. by copolymerizing a monomer having a carboxyl group with a monomer having an epoxy group and other monomer in a specified weight ratio. CONSTITUTION:2-40wt% polymerizable monomer (A) having a carboxyl group (e.g., acrylic acid), 0.1-20wt% polymerizable monomer (B) having an epoxy group (e.g., glycidyl acrylate) and 40-97.9wt% other polymerizable monomer (C) (e.g., methyl acrylate) are used in such a proportion that the combined amount of the components A, B and C is 100wt% to copolymerize them. The resulting water-soluble resin is used as an essential ingredient and additives such as a pigment, a filler, etc. are added thereto to obtain the desired sealer compsn. for inorg. porous substrates. The compsn. is non-toxic, has no fear of catching a fire and penetrates well into substrates such as mortar, concrete, etc.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は無機多孔質基材用シーラー組成物に関する。更
に詳しくは無機多孔質Lt材、例えばモルタル、コンク
リート等の基材へ通用した場合に良く含浸し、しかも優
れた補強性、耐久性及び上塗り適性を右する塗膜を与え
る無機多孔?’i基材用シーラー組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a sealer composition for inorganic porous substrates. More specifically, inorganic porous Lt materials, such as inorganic porous Lt materials, which when used in base materials such as mortar and concrete, impregnate well and provide a coating film with excellent reinforcing properties, durability, and suitability for overcoating. 'I relates to a sealer composition for base materials.

(従来の技術および発明が解決しようとする問題点) 従来無機多孔質u月のシーラーに使用する樹脂としては
比較的低分子間の湿気硬化型ウレタン、溶剤系樹脂等が
用いられていたが、前者はその11X性が、又1殻者は
有機溶剤の使用による火災の危険性や環境汚染等が問題
となってJ3す、水性化の要望が強くなっている。水系
シーラーとしては、水溶性樹脂や水分散性樹脂を主成分
とするしのが種々検討されているが、水溶性樹脂を主成
分とするものは耐水性が、又、水分散性樹脂を主成分と
するものは基材へのΩ温性や密着性が悪く、長期の耐久
性を右する水系シーラーは10られていないのが現状で
ある。
(Prior art and problems to be solved by the invention) Conventionally, moisture-curing urethane, solvent-based resins, etc. with relatively low molecular weights have been used as resins for inorganic porous sealers. The former has become a problem due to its 11X property, and the former has become a problem due to the risk of fire and environmental pollution due to the use of organic solvents, and there is a strong demand for water-based products. As water-based sealers, various types of sealers based on water-soluble resins and water-dispersible resins have been studied. Currently, there are no water-based sealers available that are important for long-term durability, as the ingredients have poor Ω temperature resistance and adhesion to the base material.

(問題点を解決するための技術的手段)本発明は上記の
様な問題点即ち、湿気硬化型ウレタンや溶剤系樹脂等を
主成分とするシーラーが有するm性、火災の危険性、環
境汚染等の問題や水系シーラが有する耐水性、含浸不良
、密着性不足の問題を一挙に解決したものである。
(Technical Means for Solving the Problems) The present invention solves the above-mentioned problems, namely, the thermal properties of sealers whose main components are moisture-curing urethane, solvent-based resins, etc., the danger of fire, and the environmental pollution. This solution solves the problems of water-based sealers such as water resistance, poor impregnation, and insufficient adhesion all at once.

即ち、本発明は、 カルボキシル基を含有する重合性1m体(a)2〜40
ffiffi%、エポキシ基を含有する重合性単量体(
b)0.1〜20重扮%及びその他の重合性単量体(c
)40〜97.91M%(但し、(a)+ (b)+ 
(c)は100重量%である)を重合して得られる水溶
性樹脂(I)を必須成分として含む無機多孔質基材用シ
ーラー組成物にI!I′rjるものである。
That is, the present invention provides 2 to 40 polymerizable 1m bodies (a) containing carboxyl groups.
ffiffi%, polymerizable monomer containing epoxy group (
b) 0.1 to 20% polymerizable monomer (c
)40 to 97.91M% (however, (a) + (b) +
(c) is 100% by weight)) is added to a sealer composition for inorganic porous substrates containing as an essential component a water-soluble resin (I) obtained by polymerizing I! I'rj.

本発明の無機多孔質基材用シーラー組成物は水溶性樹脂
(I)を主成分としてなる為に、無機多孔質基材への含
浸性が著しく優れている。しかも該水溶性樹脂(I)が
分子中にカルボキシル基とエポキシ基とを含有しており
、成膜過程においてエポキシ基同士あるいはカルボキシ
ル基とエポキシ基とが架橋反応して硬化被膜を形成する
為に、優れた耐久性を有するものである。
Since the sealer composition for inorganic porous substrates of the present invention contains water-soluble resin (I) as a main component, it has extremely excellent impregnation properties into inorganic porous substrates. Moreover, the water-soluble resin (I) contains carboxyl groups and epoxy groups in its molecules, and during the film forming process, epoxy groups or carboxyl groups and epoxy groups crosslink to form a cured film. , has excellent durability.

本発明に使用するカルボキシル基を含有する重合性単量
体(a)は分子内にカルボキシル基を有する重合性単量
体であれば特に制限されず、例えばアクリル酸、メタク
リル酸、クロトン酸、イタコン酸、マレイン酸及びモノ
メチルマレエートなどの不飽和カルボン酸類又はその誘
導体などを挙げる事ができ、これらの群から選ばれる1
種又は2種以上の混合物を使用する事ができる。該単量
体(a)は重合した後の樹脂に水溶性を付与したり、エ
ポキシ基と架橋反応する為の必須成分で、2〜40重量
%の範囲で使用する。使用量が2重重%未満の場合は得
られるalrtが水溶性となり(りず、逆に40重蚤%
を越えて多ω用いた場合は耐水性が低下するので好まし
くない。
The carboxyl group-containing polymerizable monomer (a) used in the present invention is not particularly limited as long as it is a polymerizable monomer having a carboxyl group in the molecule, such as acrylic acid, methacrylic acid, crotonic acid, itacon acid, unsaturated carboxylic acids such as maleic acid and monomethyl maleate, or derivatives thereof, and one selected from these groups.
Seeds or mixtures of two or more types can be used. The monomer (a) is an essential component for imparting water solubility to the polymerized resin and for crosslinking with epoxy groups, and is used in an amount of 2 to 40% by weight. If the amount used is less than 2% by weight, the resulting alrt will be water-soluble (on the contrary, it will be 40% by weight).
It is not preferable to use a large amount of ω in excess of ω because the water resistance decreases.

本発明に使用するエポキシ基を含有する重合性単量体(
b)は分子内にエポキシ基を有する但合性単m体であれ
ば特に制限されず、例えばグリシジルアクリレート、グ
リシジルメタクリレート及びアリルグリシジルエーテル
などを挙げる事ができ、これらの群から選ばれる1種又
は2種以上の混合物を使用する事ができる。該単量体(
b)は樹脂の基材に対する密着性を向上したり、それ同
士であるいはカルボキシル基と架橋反応する為の゛必須
成分で0.1〜20重量%の範囲で使用する。
Polymerizable monomer containing epoxy group used in the present invention (
b) is not particularly limited as long as it is a merging monomer having an epoxy group in the molecule, examples include glycidyl acrylate, glycidyl methacrylate, and allyl glycidyl ether, and one selected from these groups or A mixture of two or more types can be used. The monomer (
b) is an essential component for improving the adhesion of the resin to the substrate and crosslinking the resins with each other or with carboxyl groups, and is used in an amount of 0.1 to 20% by weight.

使用量が0.1重足%未満の場合は密着性の向上や架橋
反応性の付与の為の実質有効岳となり得ず、逆に20m
fji%を越えて多&用いた場合は液の保存安定性が低
下するので好ましくない。
If the amount used is less than 0.1% by weight, it will not be effective for improving adhesion or imparting crosslinking reactivity;
If it is used in an amount exceeding fji%, the storage stability of the liquid will decrease, which is not preferable.

本発明に使用できるその他の重合性単量体(C)は、前
記重合性tp m体(a)および(b)と共重合しうる
重合性単量体であれば特に制限されず、例えばメチルア
クリ、レート、エチルアクリレート、ブチルアクリレー
ト、2−エチルへキシルアクリレート、シクロへキシル
アクリレート、メチルメタクリレート、エチルメタクリ
レ−1・、スチレン、α−クロルスチレン、ビニルトル
エン、フッ化ビニル、塩化ビニル、アクリロニ1−リル
、メククリ口二トリル、酢酸ビニル、プロピオン酸ビニ
ル、アクロレイン、ヒドロキシエチルアクリレート、ヒ
ドロキシエチルメタクリレート、ヒドロキシプロピルア
クリレート、アクリルアミド、メタクリルアミド、ジメ
チルアミノエチルアクリレート及びジメチルアミノエチ
ルメタクリレートなどを挙げる事ができ、これらの群か
ら選ばれる1種又は2種以上の混合物を使用する事がで
きる。
Other polymerizable monomers (C) that can be used in the present invention are not particularly limited as long as they are copolymerizable with the polymerizable TP m forms (a) and (b), such as methyl acrylate. , rate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, cyclohexyl acrylate, methyl methacrylate, ethyl methacrylate-1, styrene, α-chlorostyrene, vinyltoluene, vinyl fluoride, vinyl chloride, acryloni-1 - Ryl, mekkuri nitrile, vinyl acetate, vinyl propionate, acrolein, hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, acrylamide, methacrylamide, dimethylaminoethyl acrylate and dimethylaminoethyl methacrylate, etc. One type or a mixture of two or more types selected from these groups can be used.

本発明の無機多孔質基材用シーラー組成物の必須成分で
ある水溶性樹脂(I)は上記重合性単量体(a)、(b
)及び(C)を公知の手順に従って水溶液重合してでき
る。重合開始剤としては過硫酸アンモニウム、過@酸カ
リウム、過酸化水素、ブチルハイドロパーオキサイド等
公知の水溶性もしくは水分散性の重合開始剤が使用でき
る。
The water-soluble resin (I) which is an essential component of the sealer composition for inorganic porous substrates of the present invention is composed of the above polymerizable monomers (a) and (b).
) and (C) by aqueous solution polymerization according to known procedures. As the polymerization initiator, known water-soluble or water-dispersible polymerization initiators such as ammonium persulfate, potassium persulfate, hydrogen peroxide, and butyl hydroperoxide can be used.

又、水溶性樹脂(1)は水に可溶性の有機溶剤中で溶液
重合した後、水で稀釈してもできる。この際使用できる
溶剤としては、例えばメチルアルコール、エチルアルコ
ール、n−ブチルアルゴール、イゾブチルアルコール、
n−プロビルアルコ−ル、イソプロピルアルコール、メ
チルエチルケトン、メチルイソブチルケトン、エチレン
グリコール、プロピレングリコール、エチレングリコー
ルモノメチルエーテル等を挙げる事ができ、これらの群
から選ばれる1種又は2種以上の混合物を使用する事が
できる。又、重合開始剤としては、アゾビスイソブチロ
ニトリル、ベンゾイルパーオキサイド、ブチルハイドロ
パーオキサイド等公知の重合開始剤が使用できる。
The water-soluble resin (1) can also be produced by solution polymerizing in a water-soluble organic solvent and then diluting with water. Examples of solvents that can be used in this case include methyl alcohol, ethyl alcohol, n-butyl algol, isobutyl alcohol,
Examples include n-propyl alcohol, isopropyl alcohol, methyl ethyl ketone, methyl isobutyl ketone, ethylene glycol, propylene glycol, ethylene glycol monomethyl ether, etc., and one type or a mixture of two or more types selected from these groups is used. I can do that. Further, as the polymerization initiator, known polymerization initiators such as azobisisobutyronitrile, benzoyl peroxide, butyl hydroperoxide, etc. can be used.

水溶性樹脂(I)は上記手順に従って重合した後必要に
応じ塩基性化合物で中和しても良い。使用できる塩基性
化合物としては、例えばアンモニア、トリメチルアミン
、トリエチルアミン、ジメチルエタノールアミン、ジエ
チルエタノールアミン、トリエタノールアミン、水酸化
プトリウム及び水酸化カリウム等を挙げる事ができ、こ
れらの1種又は2種以上の混合物を使用できる。
After the water-soluble resin (I) is polymerized according to the above procedure, it may be neutralized with a basic compound if necessary. Examples of basic compounds that can be used include ammonia, trimethylamine, triethylamine, dimethylethanolamine, diethylethanolamine, triethanolamine, putrium hydroxide, and potassium hydroxide, and one or more of these can be used. Mixtures can be used.

本発明の無機多孔質基材用シーラー組成物は、前記水溶
性樹脂(I)だけで構成されても良いが、必要に応じて
公知の添加剤、例えば顔料、充填剤、トナー、湿潤剤、
帯電防止剤等を配合する事は自由である。又、ポリアミ
ン等を添加して架Iユを促進する事もできる。
The sealer composition for inorganic porous substrates of the present invention may be composed only of the water-soluble resin (I), but if necessary, known additives such as pigments, fillers, toners, wetting agents,
It is free to add antistatic agents and the like. It is also possible to add a polyamine or the like to promote cross-linking.

(発明の効果) 本発明の無機多孔質基材用シーラー組成物は、水溶性樹
脂(I)を必須成分としてなる為に、毒性、火災の危険
性、環境汚染等の問題を全く右しない。そして、該シー
ラー組成物をモルタル面、コンクリート面、スレート基
材等の無機多孔質基材に塗布した場合に基材によく含浸
し、しかも必須成分たる水溶性樹脂(、I)中に含有さ
れる特定の官能基によって、基材に対する密着性、耐久
性、上塗り適性が著しく優れたものであり、従来から公
知の溶剤系樹脂や水系樹脂を主成分とするシーラーが有
していた問題点を一挙に解決したものである。
(Effects of the Invention) Since the sealer composition for inorganic porous substrates of the present invention contains the water-soluble resin (I) as an essential component, it does not pose any problems such as toxicity, fire danger, and environmental pollution. When the sealer composition is applied to an inorganic porous substrate such as a mortar surface, a concrete surface, or a slate substrate, it is well impregnated into the substrate and is not contained in the water-soluble resin (I) which is an essential component. Due to its specific functional groups, it has extremely excellent adhesion to substrates, durability, and suitability for overcoating, and it overcomes the problems of conventional sealers whose main ingredients are solvent-based resins or water-based resins. It was resolved all at once.

従って、本発明の無機多孔:?l!材用シーラー組成物
は、例えばモルタル面、コンクリート面、外壁、屋根等
屋外の補修用に好適に使用できる。又、壁材、スレート
瓦等強!l乾燥して用いる用途にも使用できる。更に、
各種無機多孔質基材用塗料、例えばアクリル系樹脂、酢
酸ビニル系樹脂、ウレタン系樹脂をバインダーとする塗
料を用いる際のブライマーとしても使用する事ができる
Therefore, the inorganic porosity of the present invention: ? l! The material sealer composition can be suitably used for outdoor repairs such as mortar surfaces, concrete surfaces, exterior walls, and roofs. Also, wall materials, slate tiles, etc. are strong! It can also be used after drying. Furthermore,
It can also be used as a brimer when using paints for various inorganic porous substrates, such as paints using acrylic resins, vinyl acetate resins, or urethane resins as binders.

(実 施 例) 以下、実施例によって本発明の詳細な説明するが、本発
明は以下の実施例によって限定されるものではない。尚
、例中の部はすべて1吊による。
(Examples) Hereinafter, the present invention will be explained in detail with reference to Examples, but the present invention is not limited to the following Examples. In addition, all parts in the example are based on one hanging.

〔実施例 1〕 撹拌器、還流冷却器、滴下ロート、′f;A度計を備え
た四ツ目フラスコにエチレングリコールモノブチルエー
テル100部を仕込んだ後、チッ素ガスを吹込みなから
tff 痒下に80℃まで昇温した。しかる後、メタク
リル酸15部、グリシジルメタクリレート10部、スチ
レン40部、エチルアクリレート35部からなる重合性
単量体混合物にアゾビスイソブチロニトリル2.5部を
溶解した混合物を2時間にわたって均一に滴下した。そ
の後更に80℃で2時間反応した。冷却後25%のアン
モニア水を12部添加し、更に水を285.5部加えて
シーラー組成物(1)を1qた。1!7られたシーラー
組成物(1)を第1表に示した無機多孔質基材上に50
CJ/rrt2塗布し、室温で3日間乾燥した後、得ら
れた被膜の密着性及び耐水性を調べた。その結果は第1
表に示した通りであった。
[Example 1] After charging 100 parts of ethylene glycol monobutyl ether into a four-eye flask equipped with a stirrer, a reflux condenser, a dropping funnel, and a temperature meter, nitrogen gas was blown into the flask. The temperature was raised to 80°C. Thereafter, a mixture of 2.5 parts of azobisisobutyronitrile dissolved in a polymerizable monomer mixture consisting of 15 parts of methacrylic acid, 10 parts of glycidyl methacrylate, 40 parts of styrene, and 35 parts of ethyl acrylate was uniformly mixed over 2 hours. dripped. Thereafter, the reaction was further carried out at 80°C for 2 hours. After cooling, 12 parts of 25% aqueous ammonia was added, and further 285.5 parts of water were added to give 1 q of sealer composition (1). 1!7 The sealer composition (1) was applied to the inorganic porous substrate shown in Table 1 for 50 minutes.
After applying CJ/rrt2 and drying at room temperature for 3 days, the adhesion and water resistance of the resulting film were examined. The result is the first
It was as shown in the table.

〔実施例 2〕 実施例1において用いたm合性jti a体温合物をイ
タコン酸5部、グリシジルメタクリレ−1−10部、ス
チレン50部およびブチルアクリレート35部とする(
但しイタコン酸は予かしめエチレングリコールモノブチ
ルエーテルに溶解させておいた。)以外は実施例1と同
じ操作をくり返して、シーラー用組成物(2)の被膜を
19たつこの被膜の密着性及び耐水性は第1表に示した
通りであった。
[Example 2] The m-composite jti a-temperature mixture used in Example 1 is made of 5 parts of itaconic acid, 1-10 parts of glycidyl methacrylate, 50 parts of styrene, and 35 parts of butyl acrylate (
However, itaconic acid was preliminarily dissolved in ethylene glycol monobutyl ether. The same operations as in Example 1 were repeated except for ) to form a film of sealer composition (2).The adhesion and water resistance of this film were as shown in Table 1.

〔実施例 3〕 撹拌器、還流冷却思、滴下ロート、温麿計を備えた四ツ
ロフラスコにイオン交換水200部を仕込んだ後、窒素
ガスを吹込みながら撹拌下に70℃まで44した。しか
る後アクリル酸25部、グリシジルアクリレート15部
、メチルメタクリレ−h 30部、メチルアクリレート
30部からなる重合性型吊体混合物を2時間にわたって
均一に滴下した。この時同時に10%の過硫酸アンモニ
ウム水溶液40部を2時間にわたって均一に滴下した。
[Example 3] After 200 parts of ion-exchanged water was charged into a Yotsuro flask equipped with a stirrer, a reflux condenser, a dropping funnel, and a thermometer, the temperature was raised to 70° C. while stirring while blowing nitrogen gas. Thereafter, a polymerizable suspension mixture consisting of 25 parts of acrylic acid, 15 parts of glycidyl acrylate, 30 parts of methyl methacrylate-h, and 30 parts of methyl acrylate was uniformly dropped over 2 hours. At the same time, 40 parts of a 10% ammonium persulfate aqueous solution was uniformly dropped over 2 hours.

その後更に70℃で2時間反応した。冷却後25%のア
ンモニア水を24部添加してシーラー組成物(3)を1
9だ。1すられたシーラー組成物(3)を第1表に示し
た無機多孔質基材上に30g/m2塗布し、室温で3日
間乾燥した後、得られた被膜の密着性及び耐水性を調べ
た。その結果は第1表に示した通りであった。
Thereafter, the reaction was further carried out at 70°C for 2 hours. After cooling, 24 parts of 25% ammonia water was added to make 1 part of the sealer composition (3).
It's 9. 1. 30 g/m2 of the smoothed sealer composition (3) was applied onto the inorganic porous substrate shown in Table 1, and after drying at room temperature for 3 days, the adhesion and water resistance of the resulting film were examined. Ta. The results were as shown in Table 1.

〔比較例 1〕 実施例1において用いた重合性用m体混合物をメタクリ
ル115部、スチレン40部およびエチルアクリレート
45部とする以外は実施例1と同じ操作をくり返して、
比較用組成物(1)の被膜を19だ。この1膜の密着性
及び耐水性は第1表に示した通りであった。
[Comparative Example 1] The same operation as in Example 1 was repeated except that the polymerizable m-isomer mixture used in Example 1 was changed to 115 parts of methacrylic, 40 parts of styrene, and 45 parts of ethyl acrylate.
The coating of comparative composition (1) was 19. The adhesion and water resistance of this film were as shown in Table 1.

(比較例 2〕 実施例1において用いた小金性単量体混合物をメタクリ
ル酸15部、グリシジルメタクリレート25部、スチレ
ン30部、エチルアクリレート30部とする以外は実施
例1と同じ操作をくり返して、比較用組成物(2)を得
た。この組成物(2)を常温で放置しておくと、ゆっく
りと増粘して行き、1週間後にはゲル化した。
(Comparative Example 2) The same operation as in Example 1 was repeated except that the small metallic monomer mixture used in Example 1 was changed to 15 parts of methacrylic acid, 25 parts of glycidyl methacrylate, 30 parts of styrene, and 30 parts of ethyl acrylate. A comparative composition (2) was obtained.When this composition (2) was left at room temperature, it slowly thickened and gelled after one week.

〔比較例 3〕 実施例1において重合性型吊体混合物をメタクリル酸4
5部、グリシジルメタアクリレ−1・10部、スチレン
10部、ブチルアクリレート35部とする以外は実施例
1と同じ操作をくり返して比較用組成物(3)の被膜を
得た。この被膜の密着性及び耐水性は第1表に示した通
りであった。
[Comparative Example 3] In Example 1, the polymerizable hanging body mixture was mixed with methacrylic acid 4
A film of Comparative Composition (3) was obtained by repeating the same operation as in Example 1, except that 5 parts of glycidyl methacrylate, 1.10 parts of glycidyl methacrylate, 10 parts of styrene, and 35 parts of butyl acrylate were used. The adhesion and water resistance of this coating were as shown in Table 1.

第   1   表 試験方法 密着性二 被膜をカッターナイフで2腑間隔で10X1
0のゴバン目を切りポリエステル製粘首テープを圧着し
た後、引剥して被膜の残存の状態を調べた。
Table 1 Test method Adhesion 2 Cut the film with a cutter knife at 10x1 intervals.
A polyester adhesive neck tape was applied by cutting a 0 mark and then peeled off to examine the remaining state of the film.

O・・・・・・被膜が全く剥離しない △・・・・・・被膜が一部剥離した ×・・・・・・被膜が全部剥離した 耐水性: 被膜を形成した各試験片を室温で7日間純水
に浸漬し、次いで室温で2日間乾燥した後上記と同様の
方法で密着性を調べた。
O: The film does not peel off at all △: The film partially peels off ×: The film completely peels off Water resistance: Each test piece on which the film was formed was placed at room temperature. After immersing in pure water for 7 days and then drying at room temperature for 2 days, adhesion was examined in the same manner as above.

O・・・・・・被l19が全く剥離しないΔ・・・・・
・被膜が一部剥離した ×・・・・・・被膜が全部剥離した 手  続  補  正  書  (自発)昭和62年 
8月 5日
O...The target l19 does not peel off at all Δ...
・Partially peeled off the coating ×・・・Procedures in which the coating completely peeled off (Voluntary) 1988
August 5th

Claims (1)

【特許請求の範囲】 1、カルボキシル基を含有する重合性単量体(a)2〜
40重量%、 エポキシ基を含有する重合性単量体(b) 0.1〜20重量%及び その他の重合性単量体(c)40〜97.9重量% (但し、(a)+(b)+(c)は100 重量%である。)を重合して得られる水溶 性樹脂(I)を必須成分として含む無機多 孔質基材用シーラー組成物。
[Claims] 1. Carboxyl group-containing polymerizable monomer (a) 2-
40% by weight, epoxy group-containing polymerizable monomer (b) 0.1 to 20% by weight, and other polymerizable monomers (c) 40 to 97.9% by weight (However, (a) + ( b) + (c) is 100% by weight.) A sealer composition for an inorganic porous substrate, which contains as an essential component a water-soluble resin (I) obtained by polymerizing .
JP10382686A 1986-05-08 1986-05-08 Sealer composition for inorganic porous substrate Pending JPS62260870A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10382686A JPS62260870A (en) 1986-05-08 1986-05-08 Sealer composition for inorganic porous substrate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10382686A JPS62260870A (en) 1986-05-08 1986-05-08 Sealer composition for inorganic porous substrate

Publications (1)

Publication Number Publication Date
JPS62260870A true JPS62260870A (en) 1987-11-13

Family

ID=14364217

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10382686A Pending JPS62260870A (en) 1986-05-08 1986-05-08 Sealer composition for inorganic porous substrate

Country Status (1)

Country Link
JP (1) JPS62260870A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0618179A2 (en) * 1993-03-27 1994-10-05 Degussa Aktiengesellschaft Prepolymer solution for protecting and stabilising impregnation of porous building materials
JP2004115678A (en) * 2002-09-26 2004-04-15 Sk Kaken Co Ltd Aqueous undercoat composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5030933A (en) * 1973-07-19 1975-03-27
JPS5035923A (en) * 1973-07-23 1975-04-04
JPS52155628A (en) * 1976-06-22 1977-12-24 Mitsubishi Electric Corp Water paint

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5030933A (en) * 1973-07-19 1975-03-27
JPS5035923A (en) * 1973-07-23 1975-04-04
JPS52155628A (en) * 1976-06-22 1977-12-24 Mitsubishi Electric Corp Water paint

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0618179A2 (en) * 1993-03-27 1994-10-05 Degussa Aktiengesellschaft Prepolymer solution for protecting and stabilising impregnation of porous building materials
EP0618179A3 (en) * 1993-03-27 1994-11-17 Degussa Prepolymer solution for protecting and stabilising impregnation of porous building materials.
JP2004115678A (en) * 2002-09-26 2004-04-15 Sk Kaken Co Ltd Aqueous undercoat composition

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