JP2000063757A - Water-based water-repellent paint and surface-finishing method for exposed concrete using the same - Google Patents

Water-based water-repellent paint and surface-finishing method for exposed concrete using the same

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Publication number
JP2000063757A
JP2000063757A JP10236910A JP23691098A JP2000063757A JP 2000063757 A JP2000063757 A JP 2000063757A JP 10236910 A JP10236910 A JP 10236910A JP 23691098 A JP23691098 A JP 23691098A JP 2000063757 A JP2000063757 A JP 2000063757A
Authority
JP
Japan
Prior art keywords
water
aqueous
parts
powder
coating material
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.)
Granted
Application number
JP10236910A
Other languages
Japanese (ja)
Other versions
JP4264146B2 (en
Inventor
Nobuhito Hirata
信人 平田
Makoto Ueda
誠 上田
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.)
Kansai Paint Co Ltd
Original Assignee
Kansai Paint 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 Kansai Paint Co Ltd filed Critical Kansai Paint Co Ltd
Priority to JP23691098A priority Critical patent/JP4264146B2/en
Publication of JP2000063757A publication Critical patent/JP2000063757A/en
Application granted granted Critical
Publication of JP4264146B2 publication Critical patent/JP4264146B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a water-based water-repellent paint that gives a coating layer having excellent resistance to alkali, water and weather and is suitably useful for surface finishing of fair-faced concrete by using a water-based silicone resin or the like, silica powder, and fluorine resin powder. SOLUTION: The objective painting material includes (A) a water-based silicone resin and/or a water-based fluorine resin such as polysiloxane complex water-based emulsion or the like that has the core part of a cross-linked polymer and the shell part that cover the core part with a non-crosslinking polymer, and has polysiloxane close to the shell surface, (B) a silica powder, preferably in an amount of 5-20 pts.wt. (based on 100 pts.wt. of the solid part of the component A) and (C) a fluorine resin powder, preferably in an amount of 5-30 pts.wt. The weight ratio of the component B to the component C is 2/1-1/4. In addition, the water-based water-repellent paint preferably contains a fungicide and an algaecide and the fair-faced concrete coated with this paint preferably gives a unique feeling and high finishing quality.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、打放しコンクリ−
トの表面に高い仕上り質感を付与し得る水性防水塗材及
びこれを用いた打放しコンクリ−トの表面仕上げ工法に
関する。
BACKGROUND OF THE INVENTION The present invention relates to an exposed concrete.
The present invention relates to a water-based waterproof coating material capable of imparting a high finish texture to the surface of a sheet and a surface finishing method for an exposed concrete using the same.

【0002】[0002]

【従来技術及びその課題】打放しコンクリ−トは、その
素材の持つ質感を生かした外壁材として広く使用されて
おり、通常、その表面には、水分の侵入を防止するため
に撥水材や溶剤型のクリヤ−が塗布されてきた。これ
は、素材面のままでは、空気中の水分により、コンクリ
−トの中性化が進行し耐久性が低下すると共に、カビや
藻が発生・付着して美観を損ね、さらに外部からもたら
される塩化物が内部の鉄筋まで侵入し腐食が進めば構造
物そのものの倒壊につながる恐れもあるためである。
BACKGROUND OF THE INVENTION Exposed concrete is widely used as an outer wall material that takes advantage of the texture of the material, and its surface is usually a water repellent material or a solvent to prevent water from entering. Mold clear has been applied. This is because when the material surface is left as it is, moisture in the air causes the concrete to neutralize and the durability to decline, and mold and algae to be generated and adhere to the aesthetics to impair the aesthetic appearance and be brought from the outside. This is because if chloride penetrates into the internal reinforcing bars and corrosion progresses, the structure itself may collapse.

【0003】従来の撥水材や溶剤型のクリヤ−を夫々単
独で用いた場合、撥水材単独では撥水保護効果の持続性
に乏しく、溶剤型クリヤ−単独では保護性はあるものの
コンクリ−ト表面が濡れ色となり素材の質感を損ね、塗
工事での有機溶剤臭や安全衛生上の問題もあった。
When conventional water-repellent materials and solvent-type clears are used individually, the water-repellent materials alone have poor sustainability of water-repellent protection, and solvent-type clears alone have a protective property but are concrete. The surface of the coating became wet and the texture of the material was impaired, and there were problems with organic solvent odor during the coating work and safety and hygiene.

【0004】これらを解決するために、例えば特公平6
−89589号、特開平5−124880号、特開平9
−173969号公報などでにおいて、撥水材と溶剤型
クリヤ−を種々塗り重ねる方法が提案されており、濡れ
色防止に効果が認められている。しかしながら特公平6
−89589号の方法では、3層仕上げで塗布工程が多
く、仕上げに溶剤型のクリヤ−を用いるため有機溶剤臭
や安全衛生上の問題があった。また特開平5−1248
80号、特開平9−173969号の方法では、撥水・
防水能がいまだ不十分であった。
In order to solve these problems, for example, Japanese Patent Publication No.
-89589, JP-A-5-124880, JP-A-9
In Japanese Patent No. 173969 and the like, a method of applying various types of water-repellent materials and solvent-type clears has been proposed, and the effect of preventing wet color is recognized. However, Tokuhei 6
In the method of No. 89895, there are many coating steps in three-layer finishing, and since a solvent type clear is used for finishing, there are problems with organic solvent odor and safety and hygiene. In addition, JP-A-5-1248
No. 80 and JP-A-9-173969, water repellency
Water resistance was still insufficient.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記問題
を解決すべく鋭意検討した結果、水性シリコ−ン系樹脂
及び/又は水性フッ素系樹脂に特定の微粉末を配合して
なる水性クリヤ−が、打放しコンクリ−トの表面の仕上
げ用として、コンクリ−トの劣化を防止するだけでな
く、独特の風合いと高い仕上り質感を付与し得ることを
見出し本発明に到達した。
Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that an aqueous silicone resin and / or an aqueous fluororesin prepared by blending a specific fine powder The present inventors have found that the clearer can not only prevent the deterioration of the concrete as a finish for the surface of the exposed concrete but also impart a unique texture and a high finished texture to the present invention.

【0006】即ち本発明は、(A)水性シリコ−ン系樹
脂及び/又は水性フッ素系樹脂、(B)シリカ粉、及び
(C)フッ素系樹脂パウダ−を含有することを特徴とす
る水性防水塗材、及び打放しコンクリ−トの表面に下塗
り材を塗布し、乾燥後、上記水性防水塗材を塗布してな
る打放しコンクリ−トの表面仕上げ工法を提供するもの
である。
That is, the present invention is characterized by containing (A) an aqueous silicone resin and / or an aqueous fluorine resin, (B) silica powder, and (C) a fluorine resin powder. The present invention provides a surface finish construction method for an exposed concrete, which comprises applying an undercoat material on the surface of a coating material and an exposed concrete, drying and then applying the above-mentioned water-based waterproof coating material.

【0007】[0007]

【発明の実施の形態】本発明において使用される水性シ
リコ−ン系樹脂及び/又は水性フッ素系樹脂(A)は、
防水被膜形成成分であり、従来公知の防水塗料用エマル
ションが特に制限なく使用できる。両者は夫々単独で、
又は併用して用いることができる。該水性シリコ−ン系
樹脂及び/又は水性フッ素系樹脂は透明性に優れている
ことが望ましい。
BEST MODE FOR CARRYING OUT THE INVENTION The water-based silicone resin and / or water-based fluororesin (A) used in the present invention is
It is a component for forming a waterproof film, and conventionally known emulsions for waterproof paints can be used without particular limitation. Both are independent,
Alternatively, they can be used in combination. It is desirable that the aqueous silicone resin and / or the aqueous fluorine resin have excellent transparency.

【0008】水性シリコ−ン系樹脂としては、例えばア
ルコキシシラン化合物やオルガノシロキサン化合物、又
はその縮合物からなるポリシロキサンを水性媒体に分
散、乳化、溶解したもの、さらにアルコキシシリル基含
有ビニルモノマ−を必要に応じて他のビニルモノマ−と
共重合してなる共重合体エマルション、有機重合体にポ
リシロキサンを複合化させてなるエマルションなどが挙
げられ、具体的な市販品としては、例えば「ポリデュレ
ックス」(旭化成社製)、「カネビノ−ル」(日本エヌ
エスシ−社製)、「サンモ−ル」(三洋化成社製)、
「KP3000S」(ジェイエスア−ル社製)、「ゼム
ラック」(鐘淵化学工業社製)などが挙げられる。
As the aqueous silicone resin, for example, a polysiloxane comprising an alkoxysilane compound, an organosiloxane compound or a condensate thereof is dispersed, emulsified or dissolved in an aqueous medium, and an alkoxysilyl group-containing vinyl monomer is required. A copolymer emulsion formed by copolymerization with another vinyl monomer, an emulsion formed by complexing an organic polymer with polysiloxane, and the like are listed as specific commercial products, for example, "Polydurex" ( Asahi Kasei), "Kanebinol" (Nippon NSC), "Sanmor" (Sanyo Kasei),
Examples thereof include "KP3000S" (manufactured by JS-Al Corporation), "Zemlac" (manufactured by Kaneka Corporation).

【0009】上記水性シリコ−ン系樹脂として、特に塗
膜の造膜性や緻密性、耐久性等の点から、架橋重合体で
あるコア部とそれを覆う非架橋重合体であるシェル部と
を有し且つ該シェルの表面近傍にポリシロキサンを有す
るポリシロキサン複合水性エマルションが好適に使用で
きる。
As the above-mentioned aqueous silicone resin, from the viewpoints of film-forming property, compactness, durability, etc. of the coating film, a core part which is a cross-linked polymer and a shell part which is a non-cross-linked polymer covering the core part are provided. And a polysiloxane composite aqueous emulsion having a polysiloxane near the surface of the shell can be preferably used.

【0010】該ポリシロキサン複合水性エマルション
は、粒子表面近傍にポリシロキサンを有する平均粒子径
が50〜1000nmの重合体エマルションである。該
重合体粒子は、1段目にジビニルベンゼンやアリルメタ
クリレ−ト、多価アクリレ−ト等の架橋性モノマ−を
0.01〜5重量%含有するモノマ−混合物を乳化重合
し、その重合体粒子存在下に2段目として該架橋性モノ
マ−を含まないモノマ−混合物を乳化重合して、得られ
る重合体粒子(シ−ド粒子)の存在下に、アルコキシシ
ラン化合物及び/又は低分子量のオルガノシロキサン化
合物を添加し、縮合反応させて得られるものである。
The polysiloxane composite aqueous emulsion is a polymer emulsion having polysiloxane in the vicinity of the particle surface and having an average particle size of 50 to 1000 nm. The polymer particles are emulsion polymerized in a first stage by emulsion polymerization of a monomer mixture containing 0.01 to 5% by weight of a crosslinkable monomer such as divinylbenzene, allyl methacrylate and polyvalent acrylate. As a second step in the presence of coalesced particles, a monomer mixture not containing the crosslinkable monomer is emulsion polymerized to obtain polymer particles (seed particles), and an alkoxysilane compound and / or a low molecular weight compound is obtained. It is obtained by adding the organosiloxane compound (1) and subjecting it to a condensation reaction.

【0011】上記1、2段目の重合に使用される架橋性
モノマ−以外の重合性モノマ−としては、例えばスチレ
ン、エチルビニルベンゼンなどの芳香族モノビニル化合
物;メチル(メタ)アクリレ−ト、エチル(メタ)アク
リレ−ト、ブチル(メタ)アクリレ−ト、2−エチルヘ
キシル(メタ)アクリレ−ト、シクロヘキシル(メタ)
アクリレ−ト、2−ヒドロキシ(メタ)アクリレ−ト、
グリシジル(メタ)アクリレ−ト、N,N−ジメチルア
ミノエチル(メタ)アクリレ−トなどの(メタ)アクリ
ル酸エステルモノマ−;(メタ)アクリル酸、マレイン
酸、無水マレイン酸などの不飽和カルボン酸;(メタ)
アクリロニトリル、ダイアセトンアクリルアミド、ダイ
アセトンメタクリルアミド、(メタ)アクリルアミド、
ビニルトリメトキシシラン、γ−(メタ)アクリロイル
オキシプロピルトリメトキシシラン、これらのマクロモ
ノマ−などが挙げられ、これらは1種又は2種以上併用
することができる。
Examples of the polymerizable monomer other than the crosslinkable monomer used in the first and second stages of polymerization include aromatic monovinyl compounds such as styrene and ethylvinylbenzene; methyl (meth) acrylate and ethyl. (Meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, cyclohexyl (meth)
Acrylate, 2-hydroxy (meth) acrylate,
(Meth) acrylic acid ester monomers such as glycidyl (meth) acrylate and N, N-dimethylaminoethyl (meth) acrylate; unsaturated carboxylic acids such as (meth) acrylic acid, maleic acid and maleic anhydride ; (Meta)
Acrylonitrile, diacetone acrylamide, diacetone methacrylamide, (meth) acrylamide,
Examples thereof include vinyltrimethoxysilane, γ- (meth) acryloyloxypropyltrimethoxysilane, and macromonomers thereof, and these may be used alone or in combination of two or more.

【0012】上記シ−ド粒子の1段目と2段目重合体の
重量比が70/30〜30/70の範囲内が適当であ
る。またシ−ド粒子重合体全体のガラス転移温度は、−
20〜80℃の範囲内が適当である。
It is suitable that the weight ratio of the first-stage polymer to the second-stage polymer of the seed particles is within the range of 70/30 to 30/70. The glass transition temperature of the whole seed particle polymer is −
The range of 20 to 80 ° C is suitable.

【0013】上記アルコキシシラン化合物及び低分子量
のオルガノシロキサン化合物としては、例えばテトラエ
トキシシラン、メチルトリメトキシシラン、メチルトリ
エトキシシラン、フェニルトリメトキシシラン、フェニ
ルトリエトキシシラン、ビニルトリメトキシシラン、γ
−グリシドキシプロピルトリメトキシシラン、γ−メル
カプトプロピルトリメトキシシラン、ジメチルジメトキ
シシランなどのアルコキシシラン化合物、「MKCシリ
ケ−トMS−51」(三菱化学社製)、「エチルシリケ
−ト48」(多摩化学社製)などのオルガノシロキサノ
リゴマ−等が挙げられ、これらは1種又は2種以上併用
することができる。
Examples of the alkoxysilane compound and the low molecular weight organosiloxane compound include tetraethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, vinyltrimethoxysilane and γ.
-Alkoxysilane compounds such as glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane and dimethyldimethoxysilane, "MKC silicate MS-51" (manufactured by Mitsubishi Chemical Corporation), "ethyl silicate 48" (Tama (Manufactured by Kagaku Co., Ltd.) and the like, and the like can be used alone or in combination of two or more.

【0014】上記アルコキシシラン化合物及びオルガノ
シロキサン化合物の添加量は、シ−ド粒子100重量部
に対して0.1〜200重量部、好ましくは10〜80
重量部の範囲内が適当である。
The amount of the above-mentioned alkoxysilane compound and organosiloxane compound added is 0.1 to 200 parts by weight, preferably 10 to 80 parts by weight, relative to 100 parts by weight of the seed particles.
A range of parts by weight is suitable.

【0015】上記シ−ド粒子中にアルコキシシラン化合
物及びオルガノシロキサン化合物を吸収させるのは、シ
−ド粒子が分散された水系分散体中にアルコキシシラン
化合物及びオルガノシロキサン化合物を少しずつ又は一
括で添加し、よく攪拌することによる。この吸収前にア
ルコキシシラン化合物及びオルガノシロキサン化合物の
縮合が進まないように、水系分散体をpH4〜10、好
ましくは6〜8、温度90℃以下、好ましくは50℃以
下とするのが望ましい。吸収後の縮合反応は、反応温
度、pHで制御し、得られるポリシロキサンの重合度を
コントロ−ルするものである。
The alkoxysilane compound and the organosiloxane compound are absorbed in the seed particles by adding the alkoxysilane compound and the organosiloxane compound little by little or at once to the aqueous dispersion in which the seed particles are dispersed. And stir well. It is desirable that the pH of the aqueous dispersion is adjusted to 4 to 10, preferably 6 to 8, and the temperature is 90 ° C or lower, preferably 50 ° C or lower so that the condensation of the alkoxysilane compound and the organosiloxane compound does not proceed before the absorption. The condensation reaction after absorption is controlled by the reaction temperature and pH to control the degree of polymerization of the obtained polysiloxane.

【0016】前記水性フッ素系樹脂としては、例えばテ
トラフルオロエチレン、トリフルオロクロロエチレンな
どのフルオロオレフィン、フッ化ビニル、フッ化ビニリ
デン、ヘキサフルオロイソブチレン、パ−フルオロ(メ
タ)アクリル酸又はそのアルキルエステル、(メタ)ア
クリル酸のフルオロアルキルエステル、パ−フルオロビ
ニルエ−テル、パ−フルオロアルキルビニルエ−テルな
どのフッ素含有モノマ−と、シクロヘキシルビニルエ−
テル、アルキルビニルエ−テル、ヒドロキシアルキルビ
ニルエ−テル、脂肪族カルボン酸ビニルエステル、ヒド
ロキシアルキルビニルエステルなどとの共重合体を、水
性媒体に溶解、分散、乳化したものが挙げられる。該水
性フッ素系樹脂の市販品としては、例えば「セフラルコ
−ト」(セントラル硝子社製)、「ゼッフル」(ダイキ
ン工業社製)、「フルオネ−ト」(大日本インキ化学工
業社製)、「ルミフロン」(旭硝子社製)などが使用で
きる。
Examples of the above-mentioned aqueous fluororesins include fluoroolefins such as tetrafluoroethylene and trifluorochloroethylene, vinyl fluoride, vinylidene fluoride, hexafluoroisobutylene, perfluoro (meth) acrylic acid or alkyl esters thereof. Fluorine-containing monomers such as fluoroalkyl ester of (meth) acrylic acid, perfluorovinyl ether, and perfluoroalkyl vinyl ether, and cyclohexyl vinyl ether.
Examples thereof include those obtained by dissolving, dispersing, and emulsifying a copolymer with a ter, an alkyl vinyl ether, a hydroxyalkyl vinyl ether, an aliphatic carboxylic acid vinyl ester, a hydroxyalkyl vinyl ester and the like in an aqueous medium. Commercially available products of the aqueous fluororesin include, for example, "Cefural Coat" (manufactured by Central Glass Co., Ltd.), "Zeffle" (manufactured by Daikin Industries, Ltd.), "Fluoronet" (manufactured by Dainippon Ink and Chemicals Co., Ltd.), Lumiflon "(manufactured by Asahi Glass Co., Ltd.) can be used.

【0017】本発明において使用されるシリカ粉(B)
は、塗面の艶消し感の向上に寄与するものであり、通
常、1.0〜20μmの粒子径を有するものが使用でき
る。該シリカ粉としては、例えば「サイリシア」(富士
シリシア化学社製)、「カ−プレックス」(塩野義製薬
社製)、「シリカフラワ−」(益見製粉社製)、「アエ
ロジル」(日本アエロジル社製)、「フラッティングエ
イジェント」(デグサ社製)などの市販品が使用でき
る。
Silica powder (B) used in the present invention
Contributes to improving the matte feeling of the coated surface, and particles having a particle diameter of 1.0 to 20 μm can be usually used. Examples of the silica powder include "Sylysia" (manufactured by Fuji Silysia Chemical Ltd.), "Carplex" (manufactured by Shionogi Pharmaceutical Co., Ltd.), "Silica Flower" (manufactured by Masumi Milling Co., Ltd.), "Aerosil" (Nippon Aerosil Co., Ltd.) Commercially available products such as "made by" and "Flatting Agent" (made by Degussa) can be used.

【0018】上記シリカ粉(B)の含有量は、上記
(A)成分の固形分100重量部に対して5〜20重量
部、好ましくは7〜15重量部が好適である。該含有量
が5重量部未満では、得られる塗面の艶消し感の発現が
不十分であり、一方20重量部を越えると得られる塗膜
の耐アルカリ性、耐水性が低下するので好ましくない。
該シリカ粉の塗材への添加は、水溶性樹脂などの分散樹
脂や界面活性剤などを用いてサンドミル等の分散機で水
分散化して塗材中に添加することにより行なうことがで
きる。
The content of the silica powder (B) is 5 to 20 parts by weight, preferably 7 to 15 parts by weight, based on 100 parts by weight of the solid content of the component (A). When the content is less than 5 parts by weight, the matte feeling of the coated surface obtained is insufficient, while when it exceeds 20 parts by weight, the alkali resistance and water resistance of the obtained coating film are deteriorated, which is not preferable.
The silica powder can be added to the coating material by water-dispersing it with a dispersing machine such as a sand mill using a dispersing resin such as a water-soluble resin or a surfactant.

【0019】本発明において使用されるフッ素系樹脂パ
ウダ−(C)は、艶調整剤として打放しコンクリ−ト面
の質感を向上させるものであり、通常、1.0〜10μ
mの粒子径を有するものが使用できる。該フッ素系樹脂
パウダ−としては、例えば「シャムロック」(シャムロ
ックテクノロジ−社製)、「ホスタフロン」(ヘキスト
ジャパン社製)などの市販品が使用できる。
The fluorine-based resin powder (C) used in the present invention is used as a luster modifier to improve the texture of the concrete surface and is usually 1.0 to 10 μm.
Those having a particle size of m can be used. As the fluororesin powder, commercially available products such as "Shamrock" (manufactured by Shamrock Technology) and "Hostaflon" (manufactured by Hoechst Japan) can be used.

【0020】上記フッ素系樹脂パウダ−(C)の含有量
は、上記(A)成分の固形分100重量部に対して5〜
30重量部、好ましくは7〜20重量部が好適である。
該含有量が5重量部未満では、適度な質感(スリック
感)と艶消し感の発現が不十分となり、一方30重量部
を越えると該塗材を2回塗りする際に1層目と2層目の
密着性が低下するので好ましくない。該フッ素系樹脂パ
ウダ−の塗材への添加は、水溶性樹脂などの分散樹脂や
界面活性剤などを用いてサンドミル等の分散機で水分散
化して粗粒子を除いてから塗材中に添加することにより
行なうことができる。
The content of the fluororesin powder (C) is 5 to 100 parts by weight of the solid content of the component (A).
30 parts by weight, preferably 7 to 20 parts by weight are suitable.
When the content is less than 5 parts by weight, the appropriate texture (slick feeling) and the matte feeling are not sufficiently exhibited, while when it exceeds 30 parts by weight, the first layer and the second layer are applied when the coating material is applied twice. It is not preferable because the adhesiveness of the layers decreases. The fluororesin powder is added to the coating material by water-dispersing it with a disperser such as a sand mill using a dispersion resin such as a water-soluble resin or a surfactant to remove coarse particles and then adding it to the coating material. It can be done by doing.

【0021】本発明では上記シリカ粉(B)とフッ素系
樹脂パウダ−(C)を、重量比で2:1〜1:4、好ま
しくは1:1〜1:2の範囲内で用いることが好まし
い。該重量比よりシリカ粉が少ないと艶消し感の発現が
不十分となり、一方該重量比よりフッ素系樹脂パウダ−
が少ないと質感(スリック感)と艶消し感が不十分なだ
けでなく塗膜の耐アルカリ性、耐水性、耐候性が低下す
るので好ましくない。
In the present invention, the silica powder (B) and the fluororesin powder (C) are used in a weight ratio of 2: 1 to 1: 4, preferably 1: 1 to 1: 2. preferable. When the amount of silica powder is less than the weight ratio, the matte feeling is insufficiently expressed, while on the other hand, the fluorine-based resin powder is used in the weight ratio.
A small amount is not preferable because not only the texture (slick feeling) and matte feeling are insufficient, but also the alkali resistance, water resistance and weather resistance of the coating film deteriorate.

【0022】本発明の水性防水塗材は、上記(A)、
(B)及び(C)成分を含有する水性クリヤ−であり、
さらに必要に応じて防カビ剤及び/又は防藻剤を含有し
てもよい。
The water-based waterproof coating material of the present invention comprises the above (A),
An aqueous clear containing components (B) and (C),
Further, it may contain a fungicide and / or an algaeproofing agent, if necessary.

【0023】防カビ剤及び/又は防藻剤としては、塗材
の透明性を妨げないものであれば特に制限なく従来公知
のものが使用でき、例えば3−(3,4−ジクロロフェ
ニル)−1,1−ジメチルウレア(通称diuron又
はDCMU)、3−(3,4−ジクロロフェニル)−1
−メチルオキシ−1−メチルウレア(通称linuro
n)などのジクロロフェニル尿素化合物;2−メチルチ
オ−4−t−ブチルアミノ−6−シクロプロピルアミノ
−1,3,5−トリアジンなどのトリアジン−チオ化合
物;2−(4−チアゾリル)−ベンゾイミダゾ−ル(通
称チアベンゾ−ル)、2−メトキシカルボニルアミノベ
ンゾイミダゾ−ルなどが挙げられ、また市販品として
は、「バイオカット」(大日本インキ化学工業社製)、
「モニサイド」(武田薬品工業社製)、「プリベント−
ル」(バイエル・ジャパン社製)などが挙げられ、これ
らは1種又は2種以上併用することができる。
As the antifungal agent and / or antialgal agent, any conventionally known one can be used without particular limitation as long as it does not impair the transparency of the coating material, for example, 3- (3,4-dichlorophenyl) -1. , 1-Dimethylurea (commonly known as diuron or DCMU), 3- (3,4-dichlorophenyl) -1
-Methyloxy-1-methylurea (commonly called linuro
n) and other dichlorophenylurea compounds; 2-methylthio-4-t-butylamino-6-cyclopropylamino-1,3,5-triazine and other triazine-thio compounds; 2- (4-thiazolyl) -benzimidazo- (Commonly known as thiabenzol), 2-methoxycarbonylaminobenzimidazole, and the like, and examples of commercially available products include "Biocut" (manufactured by Dainippon Ink and Chemicals, Inc.),
"Moniside" (manufactured by Takeda Pharmaceutical Co., Ltd.), "Prevent-
("Made by Bayer Japan"), and these may be used alone or in combination of two or more.

【0024】上記防カビ剤及び/又は防藻剤の含有量
は、上記(A)成分の固形分100重量部に対して0.
5〜5重量部、好ましくは1〜2重量部が適当である。
これらは水溶性樹脂などの分散樹脂や界面活性剤などを
用いて水分散化して塗材中に添加することができる。
The content of the antifungal agent and / or the algae preventive agent is 0. 0 based on 100 parts by weight of the solid content of the component (A).
5 to 5 parts by weight, preferably 1 to 2 parts by weight are suitable.
These can be dispersed in water using a dispersion resin such as a water-soluble resin or a surfactant and added to the coating material.

【0025】本発明の水性防水塗材には、さらに必要に
応じて消泡剤、防腐剤、増粘剤、凍結防止剤、造膜助
剤、有機溶剤などの塗料用添加剤を透明性を損なわない
範囲で添加することができる。
If necessary, the water-based waterproof coating material of the present invention may further contain a paint additive such as an antifoaming agent, an antiseptic agent, a thickening agent, an antifreezing agent, a film-forming aid, and an organic solvent for transparency. It can be added within a range that does not impair it.

【0026】本発明の表面仕上げ工法は、打放しコンク
リ−トの表面に、下塗り材を塗布し、乾燥後、上記の通
り得られる水性防水塗材を塗布するものである。
In the surface finishing method of the present invention, the undercoat material is applied to the surface of the exposed concrete, and after drying, the aqueous waterproof coating material obtained as described above is applied.

【0027】上記下塗り材は、コンクリ−ト表面の微細
な斑点やピンホ−ル等の吸水部分を遮断し、撥水性・防
水性を付与するものであり、従来公知の撥水材や防水材
が使用でき、例えば前述のアルキルアルコキシシラン化
合物及び低分子量のオルガノシロキサン化合物などを水
性媒体に分散、乳化、溶解したもの、該アルキルアルコ
キシシラン化合物やフルオロアルキルアルコキシシラン
化合物などを有機溶剤で溶解・希釈したものなどが挙げ
られる。
The above-mentioned undercoating material blocks water-absorbing portions such as fine spots and pinholes on the concrete surface to impart water repellency and waterproofness. It can be used, for example, the above-mentioned alkylalkoxysilane compound and low-molecular-weight organosiloxane compound are dispersed, emulsified and dissolved in an aqueous medium, and the alkylalkoxysilane compound and fluoroalkylalkoxysilane compound are dissolved and diluted with an organic solvent. Things are included.

【0028】該下塗り材の塗布は、従来公知の塗装手
段、例えばロ−ラ−塗り、刷毛塗り、スプレ−塗装など
によって行なわれ、その塗布量は、通常、0.05〜
0.15kg/m2 程度である。
The coating of the undercoat material is carried out by a conventionally known coating means such as roller coating, brush coating, spray coating and the like, and the coating amount thereof is usually from 0.05 to
It is about 0.15 kg / m 2 .

【0029】上記水性防水塗材の塗布も、従来公知の塗
装手段、例えばロ−ラ−塗り、刷毛塗り、スプレ−塗装
などによって行なわれ、その塗布量は、通常、0.08
〜0.16kg/m2 ・回程度である。
The above-mentioned water-based waterproof coating material is also applied by a conventionally known coating means such as roller coating, brush coating, spray coating, etc. The coating amount is usually 0.08.
It is about 0.16 kg / m 2 · times.

【0030】[0030]

【実施例】以下、実施例を挙げて本発明をさらに詳細に
説明する。尚、以下「部」及び「%」はそれぞれ「重量
部」及び「重量%」を示す。
EXAMPLES The present invention will be described in more detail with reference to examples. In the following, "part" and "%" mean "part by weight" and "% by weight", respectively.

【0031】製造例1 2リットルの4つ口フラスコにコンデンサ−、温度計、
滴下ロ−トを取り付け、脱イオン水50部、ドデシルベ
ンゼンスルホン酸ソ−ダ2部を仕込み、内部の空気を窒
素で置換した後、攪拌しつつ内部温度を82℃までに上
げ溶解させた。別容器で脱イオン水20部、ドデシルべ
ンゼンスルホン酸ソ−ダ3.5部、ペルオキシ2硫酸ア
ンモニウム0.15部を添加し、よく攪拌して泡立て、
その中にシクロヘキシルメタクリレ−ト7.5部、メチ
ルメタクリレ−ト21.9部、n−ブチルアクリレ−ト
7.5部、2−エチルヘキシルアクリレ−ト12.9
部、1,6−ヘキサンジオ−ルジアクリレ−ト0.2部
のモノマ−混合液を加えて攪拌し乳化物を作り、それを
2時間を要して連続滴下した。滴下終了後、82℃で1
時間攪拌した。
Production Example 1 A 2 liter four-necked flask was equipped with a condenser, a thermometer,
A dropping funnel was attached, 50 parts of deionized water and 2 parts of sodium dodecylbenzenesulfonate were charged, and after replacing the internal air with nitrogen, the internal temperature was raised to 82 ° C. with stirring to dissolve it. In a separate container, add 20 parts of deionized water, 3.5 parts of sodium dodecyl benzene sulfonate, and 0.15 parts of ammonium peroxydisulfate, and stir well to foam.
Among them, 7.5 parts of cyclohexyl methacrylate, 21.9 parts of methyl methacrylate, 7.5 parts of n-butyl acrylate, 12.9 of 2-ethylhexyl acrylate.
And 0.2 part of 1,6-hexanediol diacrylate were added and stirred to prepare an emulsion, which was continuously added dropwise over 2 hours. After finishing the dropping, 1 at 82 ℃
Stir for hours.

【0032】次に別容器で脱イオン水20部、ドデシル
べンゼンスルホン酸ソ−ダ3.5部、ペルオキシ2硫酸
アンモニウム0.15部を添加し、よく攪拌して泡立
て、その中にシクロヘキシルメタクリレ−ト7.5部、
メチルメタクリレ−ト27.5部、n−ブチルアクリレ
−ト4.5部、2−エチルヘキシルアクリレ−ト5部、
ダイアセトンアクリルアミド2.5部、2−ヒドロキシ
エチルアクリレ−ト2部、アクリル酸1部のモノマ−混
合液を加えて攪拌し乳化物を作り、それを2時間を要し
て上記反応容器中へ連続滴下した。滴下終了後、82℃
で2時間攪拌した後、40℃まで冷却し、共重合体エマ
ルションを得た。
Next, 20 parts of deionized water, 3.5 parts of sodium dodecylbenzene sulfonate and 0.15 part of ammonium peroxydisulfate were added in a separate container, and the mixture was well stirred to foam, and cyclohexylmethacrylate was added thereto. -To 7.5 copies,
27.5 parts of methyl methacrylate, 4.5 parts of n-butyl acrylate, 5 parts of 2-ethylhexyl acrylate,
2.5 parts of diacetone acrylamide, 2 parts of 2-hydroxyethyl acrylate, and 1 part of acrylic acid were added to the monomer mixture and stirred to form an emulsion, which was allowed to take 2 hours in the above reaction vessel. Was continuously added dropwise. 82 ° C after completion of dropping
After stirring for 2 hours, the mixture was cooled to 40 ° C. to obtain a copolymer emulsion.

【0033】次に25℃に保った状態で系のpHをアン
モニア水によって7に調整し、フェニルトリメトキシシ
ラン10部を添加し、約1時間にわたって攪拌した。そ
の後、反応容器を80℃に昇温し3時間反応させて水性
エマルション(A−1)を得た。該エマルションの固形
分濃度は53%、粒子径は0.15μmであった。
Next, while maintaining the temperature at 25 ° C., the pH of the system was adjusted to 7 with aqueous ammonia, 10 parts of phenyltrimethoxysilane was added, and the mixture was stirred for about 1 hour. Then, the reaction container was heated to 80 ° C. and reacted for 3 hours to obtain an aqueous emulsion (A-1). The solid content concentration of the emulsion was 53%, and the particle size was 0.15 μm.

【0034】製造例2〜4 製造例1において、各段階のモノマ−、シラン化合物の
配合組成を表1に示す通りとする以外は製造例1と同様
の操作で、各水性エマルション(A−2)〜(A−4)
を得た。これらの性状値も表1に合わせて示す。
Production Examples 2 to 4 Each of the aqueous emulsions (A-2) was prepared in the same manner as in Production Example 1 except that the composition of the monomer and silane compound at each stage was changed as shown in Table 1. ) ~ (A-4)
Got These property values are also shown in Table 1.

【0035】[0035]

【表1】 [Table 1]

【0036】水性防水塗材の作成 実施例1〜11及び比較例1、2 表2に示す配合組成で攪拌・混合して各水性防水塗材を
得た。表2における(注1)〜(注9)は次の通りであ
る。
Preparation of Aqueous Waterproof Coating Material Examples 1 to 11 and Comparative Examples 1 and 2 Aqueous waterproof coating materials were obtained by stirring and mixing with the compounding compositions shown in Table 2. (Note 1) to (Note 9) in Table 2 are as follows.

【0037】(注1)「KP3000S」:シリコ−ン
樹脂エマルション、日本合成ゴム社製、固形分濃度45
% (注2)「ポリデュレックスG633」:シリコ−ン樹
脂エマルション、旭化成社製、固形分濃度46% (注3)「セフラルコ−トWH351D」:フッ素樹脂
エマルション、セントラル硝子社製、固形分濃度45% (注4)「サイリシア400」:シリカ粉、粒径7μ
m、富士シリシア社製 (注5)「シャムロックLF」:フッ素系樹脂パウダ
−、粒径5μm、シャムロックテクノロジ−社製 (注6)「バイオカットHG」:防藻・防カビ剤、大日
本インキ化学工業社製 (注7)「SNデフォ−マ−318」:消泡剤、サンノ
プコ社製 (注8)「アデカノ−ルUH420」:増粘剤、旭電化
工業社製 (注9)「キョ−ワノ−ルD」:造膜助剤、協和発酵社
(Note 1) "KP3000S": Silicone resin emulsion, manufactured by Japan Synthetic Rubber Co., Ltd., solid content concentration 45
% (Note 2) "Polydurex G633": Silicone resin emulsion, manufactured by Asahi Kasei Co., solid content concentration 46% (Note 3) "Sephralcoat WH351D": Fluororesin, Central Glass Co., solid content concentration 45 % (Note 4) "Sylysia 400": Silica powder, particle size 7μ
m, Fuji Silysia's (Note 5) "Shamrock LF": Fluorine resin powder, particle size 5 μm, Shamrock Technology's (Note 6) "Biocut HG": Anti-algae and antifungal agent, large Nippon Ink Chemical Co., Ltd. (Note 7) "SN Defoma-318": Defoamer, San Nopco (Note 8) "Adecan UH420": Thickener, Asahi Denka Kogyo (Note 9) "Kyowanol D": film-forming auxiliary, manufactured by Kyowa Hakko Co., Ltd.

【0038】[0038]

【表2】 [Table 2]

【0039】塗装 実施例12〜24及び比較例3、4 下地板として70×150×5mmのフレキシブル板を
用意し、〜の下塗り材を表3の通り選択し塗布量
0.08〜0.1kg/m2の範囲でローラー塗りし、
室温(20℃)で1日間乾燥させた後、上記実施例及び
比較例で得た水性防水塗材を表3の通り選択しウ−ルロ
−ラ−にて塗布量0.1〜0.12kg/m2の範囲で
2回塗りし、室温・湿度65%下の養生室にて2週間乾
燥させて各試験体を得た。
Coating Examples 12 to 24 and Comparative Examples 3 and 4 A flexible plate of 70 × 150 × 5 mm was prepared as a base plate, the undercoat material of was selected as shown in Table 3, and the coating amount was 0.08 to 0.1 kg. Roller coating in the range of / m 2
After drying at room temperature (20 ° C.) for 1 day, the water-based waterproof coating material obtained in the above Examples and Comparative Examples was selected as shown in Table 3, and the coating amount was 0.1 to 0.12 kg by a wheel roller. Each test piece was obtained by applying twice in the range of / m 2 and drying in a curing room at room temperature and a humidity of 65% for 2 weeks.

【0040】比較例5 下地板として70×150×5mmのフレキシブル板
に、を塗布量0.08〜0.1kg/m2の範囲でロ
ーラー塗りし、室温で1日乾燥後、次いで「アレスガ−
ドクリスタル」(関西ペイント社製、ヌレ色防止塗材)
をロ−ラ−にて塗布量0.12〜0.15kg/m2
範囲で塗装し1日間乾燥して、さらに「アレスガ−ドN
Fクリヤ−」(関西ペイント社製、フッ素樹脂系クリヤ
−塗料)をロ−ラ−にて塗布量0.12〜0.13kg
/m2の範囲で2回塗りし、室温・湿度65%下の養生
室にて2週間乾燥させて試験体を得た。
Comparative Example 5 As a base plate, a flexible plate of 70 × 150 × 5 mm was roller coated with a coating amount of 0.08 to 0.1 kg / m 2 and dried at room temperature for 1 day, and then "Aresgar-
De Crystal "(Kansai Paint Co., Ltd., a wet color prevention coating material)
Was coated with a roller at a coating amount of 0.12 to 0.15 kg / m 2 and dried for 1 day.
F clear "(a fluororesin clear paint manufactured by Kansai Paint Co., Ltd.) applied by a roller at an amount of 0.12 to 0.13 kg.
/ M 2 was applied twice, and dried in a curing room at room temperature and a humidity of 65% for 2 weeks to obtain a test body.

【0041】比較例6 下地板として70×150×5mmのフレキシブル板
に、を塗布量0.08〜0.1kg/m2の範囲でロ
ーラー塗りし、室温で1日乾燥後、「ボンフロンACド
ライ中塗り」(旭硝子コ−トアンドレジン社製、ウレタ
ン系中塗り塗料)をロ−ラ−にて塗布量0.1〜0.1
2kg/m2の範囲で塗装し1日間乾燥して、さらに
「ボンフロンAC#1100クリヤ−」(旭ガラスコ−
トアンドレジン社製、フッ素樹脂系クリヤ−塗料)をロ
−ラ−にて塗布量0.1〜0.11kg/m2の範囲で
2回塗りし、室温・湿度65%下の養生室にて2週間乾
燥させて試験体を得た。
Comparative Example 6 A 70 × 150 × 5 mm flexible plate as a base plate was coated with a roller in a coating amount range of 0.08 to 0.1 kg / m 2 and dried at room temperature for 1 day, followed by “Bonflon AC Dry”. "Intermediate coating" (Urethane-based intermediate coating by Asahi Glass Coat Andresin Co., Ltd.) applied by a roller at an amount of 0.1 to 0.1
Painted in the range of 2 kg / m 2 and dried for 1 day, and then "Bonflon AC # 1100 clear" (Asahi Glass Co-
Fluorine resin clear paint manufactured by Toandresin Co., Ltd. was applied twice with a roller at an application amount of 0.1 to 0.11 kg / m 2 and then in a curing room at room temperature and a humidity of 65%. A test body was obtained by drying for a week.

【0042】得られた各試験体を下記性能試験に供し評
価した。結果を表3に示す。
Each of the obtained test pieces was subjected to the following performance test and evaluated. The results are shown in Table 3.

【0043】(下塗り材) 「アレスガ−ドリパルサ−」:関西ペイント社製、撥
水性下塗り材 「アクアシ−ル200S」:住友精化社製、撥水性下
塗り材 「エポクリ−トMH−15」:日本触媒社製、エポキ
シ型下地補強剤 (性能試験) (*1)光沢:60°反射率を測定した。
(Undercoating material) "Alesgard pulsar": manufactured by Kansai Paint Co., Ltd., water-repellent undercoating material "Aqua Acyl 200S": manufactured by Sumitomo Seika, water-repellent undercoating material "Epocrete MH-15": Japan Epoxy type underlayer reinforcing agent manufactured by Catalyst Co., Ltd. (performance test) (* 1) Gloss: 60 ° The reflectance was measured.

【0044】(*2)耐水性:各試験体を室温20℃環
境下の恒温流水水槽に7日間浸漬後の塗膜状態を目視で
判定した。
(* 2) Water resistance: Each test body was visually evaluated for the state of the coating film after being immersed in a constant temperature running water bath at room temperature of 20 ° C. for 7 days.

【0045】 ◎:異常なし ○:フクレ、変色等が極僅か認められるが、実用上の支
障がない △:フクレ、変色等が一部分に認められる ×:フクレ、変色等が著しく認められる (*3)耐アルカリ性:各試験体を室温20℃環境下で
水酸化カルシウムの飽和水溶液を満たした水槽に30日
間浸漬後の塗膜状態を目視で判定した。
⊚: No abnormality ○: Very slight blistering, discoloration, etc., but no problem in practical use △: Blistering, discoloration, etc. partially observed ×: Remarkably blistering, discoloration (* 3) ) Alkali resistance: Each sample was immersed in a water tank filled with a saturated aqueous solution of calcium hydroxide at room temperature of 20 ° C. for 30 days, and the state of the coating film was visually determined.

【0046】 ◎:異常なし ○:フクレ、変色、ツヤ変化等が僅か認められるが実用
上の支障がない △:フクレ、変色、ツヤ変化等が一部分に認められる ×:フクレ、変色、ツヤ変化等が著しく認められる (*4)層間付着性:各試験体で水性防水塗材を2回塗
りした1回目と2回目の間の付着性を、JIS K 5
400のクロスカットに準じて試験を行なった。見づら
い部分については拡大鏡にて確認した。
⊚: No abnormality ○: Slight blistering, discoloration, gloss change, etc. are observed, but there is no problem in practical use △: Swelling, discoloration, gloss change, etc. are partially observed ×: Blistering, discoloration, gloss change, etc. (* 4) Interlayer adhesion: The adhesion between the first and second application of the water-based waterproof coating material twice on each test piece was measured according to JIS K 5
The test was performed according to 400 crosscuts. The part that was difficult to see was confirmed with a magnifying glass.

【0047】 ◎:全く剥離が認められない ○:カッタ−傷の塗膜の一部に剥離が認められるが実用
上の支障がない △:25%以下の塗膜に剥離が認められる ×:25%を越える塗膜に剥離が認められる (*5)促進耐候性:各試験体をサンシャインウェザ−
メ−タ−に2000時間供し、その塗膜状態を目視で判
定した。
⊚: No peeling was observed at all ○: Peeling was observed on a part of the coating film due to the cutter-scratch, but there was no problem in practical use Δ: Peeling was observed on the coating film of 25% or less ×: 25 % Peeling is observed in the coating film exceeding 5% (* 5) Accelerated weathering resistance: Each test piece was sunshine weathered.
The film was put on a meter for 2000 hours, and the state of the coating film was visually judged.

【0048】 ◎:異常なし ○:フクレ、変色、ツヤ変化、ハガレ等が僅か認められ
るが実用上の支障がない △:フクレ、変色、ツヤ変化、ハガレ等が一部分に認め
られる ×:フクレ、変色、ツヤ変化、ハガレ等が著しく認めら
れる (*6)濡れ色性:塗装前のフレキシブル板の色相に対
して、塗装により濡れ色感が生じたかどうかを目視にて
判定した。
⊚: No abnormality ○: Blisters, discoloration, gloss change, peeling, etc. are slightly observed, but there is no problem in practical use Δ: Blisters, discoloration, gloss change, peeling, etc. are partially observed ×: Blisters, discoloration Remarkably, gloss change, peeling, etc. are recognized (* 6) Wetting colorability: It was visually determined whether or not a wet color feeling was caused by coating with respect to the hue of the flexible plate before coating.

【0049】 ◎:全く変化なし ○:濡れ色感が僅かに見られるが実用上の支障がない △:黒味を帯び、濡れ色感が見られる ×:塗装前のフレキシブル板の色相と全く異なり強く黒
味を帯びている (*7)塗装時の臭気:塗装時の有機溶剤臭を評価し
た。
⊚: No change at all ○: Wet color is slightly observed but there is no problem in practical use Δ: Blackish and wet color is seen ×: Completely different from the hue of the flexible plate before coating Strongly blackish (* 7) Odor during coating: The organic solvent odor during coating was evaluated.

【0050】 ◎:全く溶剤臭がない ○:僅かに溶剤臭が感じられるが実用上の支障がない △:溶剤臭がはっきり感じられる ×:溶剤臭が強く不快である[0050] ⊚: No solvent odor ◯: Slight solvent odor is felt, but there is no problem in practical use △: Solvent odor is clearly felt ×: Strong solvent odor and uncomfortable

【0051】[0051]

【発明の効果】本発明の水性防水塗材を、打放しコンク
リ−トの表面の仕上げ用として適用すれば、耐アルカリ
性、耐水性、耐候性に優れた塗膜を形成しコンクリ−ト
の劣化を防止するだけでなく、独特の風合いと高い仕上
り質感を付与し得るものである。
When the water-based waterproof coating material of the present invention is applied for finishing the surface of an exposed concrete, a coating film excellent in alkali resistance, water resistance and weather resistance is formed to prevent deterioration of the concrete. Not only can it be prevented, but it can also impart a unique texture and a high-quality finished texture.

【0052】[0052]

【表3】 [Table 3]

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C09D 5/14 C09D 5/14 127/12 127/12 Fターム(参考) 4D075 CA38 DA06 DB12 DC03 EA06 EA13 EB16 EB43 EB56 EC03 EC54 EC60 4J038 CD092 CD101 CD121 DL031 HA446 KA20 MA02 MA08 MA10 PA07 PC04 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) C09D 5/14 C09D 5/14 127/12 127/12 F term (reference) 4D075 CA38 DA06 DB12 DC03 EA06 EA13 EB16 EB43 EB56 EC03 EC54 EC60 4J038 CD092 CD101 CD121 DL031 HA446 KA20 MA02 MA08 MA10 PA07 PC04

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】(A)水性シリコ−ン系樹脂及び/又は水
性フッ素系樹脂、(B)シリカ粉、及び(C)フッ素系
樹脂パウダ−を含有することを特徴とする水性防水塗
材。
1. An aqueous waterproof coating material comprising (A) an aqueous silicone resin and / or an aqueous fluorine resin, (B) silica powder, and (C) a fluorine resin powder.
【請求項2】 樹脂(A)が、架橋重合体であるコア部
とそれを覆う非架橋重合体であるシェル部とを有し且つ
該シェルの表面近傍にポリシロキサンを有するポリシロ
キサン複合水性エマルションである請求項1記載の水性
防水塗材。
2. A polysiloxane composite aqueous emulsion in which the resin (A) has a core part which is a cross-linked polymer and a shell part which is a non-cross-linked polymer which covers the core part and which has polysiloxane near the surface of the shell. The water-based waterproof coating material according to claim 1.
【請求項3】 シリカ粉(B)の含有量が、樹脂(A)
の固形分100重量部に対して5〜20重量部である請
求項1記載の水性防水塗材。
3. The content of the silica powder (B) is the resin (A).
The water-based waterproof coating material according to claim 1, which is 5 to 20 parts by weight with respect to 100 parts by weight of the solid content.
【請求項4】 フッ素系樹脂パウダ−の含有量(C)
が、樹脂(A)の固形分100重量部に対して5〜30
重量部である請求項1記載の水性防水塗材。
4. A content (C) of a fluorine resin powder.
Is 5 to 30 relative to 100 parts by weight of the solid content of the resin (A).
The water-based waterproof coating material according to claim 1, which is parts by weight.
【請求項5】 シリカ粉(B)とフッ素系樹脂パウダ−
(C)とを、重量比で2:1〜1:4で用いてなる請求
項1記載の水性防水塗材。
5. Silica powder (B) and fluororesin powder
The water-based waterproof coating material according to claim 1, wherein (C) is used in a weight ratio of 2: 1 to 1: 4.
【請求項6】 防カビ剤及び/又は防藻剤を含有する請
求項1記載の水性防水塗材。
6. The water-based waterproof coating material according to claim 1, which contains an antifungal agent and / or an antialgal agent.
【請求項7】 打放しコンクリ−トの表面に、下塗り材
を塗布し、乾燥後、(A)水性シリコ−ン系樹脂及び/
又は水性フッ素系樹脂、(B)シリカ粉、及び(C)フ
ッ素系樹脂パウダ−を含有する水性防水塗材を塗布する
ことを特徴とする打放しコンクリ−トの表面仕上げ工
法。
7. An undercoating material is applied to the surface of an exposed concrete, and after drying, (A) an aqueous silicone resin and / or
Alternatively, a method for finishing the surface of an exposed concrete is characterized in that an aqueous waterproof coating material containing an aqueous fluororesin, (B) silica powder, and (C) fluororesin powder is applied.
JP23691098A 1998-08-24 1998-08-24 Water-based waterproof coating material, and surface finish method for releasing concrete using the same Expired - Lifetime JP4264146B2 (en)

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Country Link
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JP2005218914A (en) * 2004-02-03 2005-08-18 Sk Kaken Co Ltd Coating method for exposed surface of concrete
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Publication number Priority date Publication date Assignee Title
JP2005218914A (en) * 2004-02-03 2005-08-18 Sk Kaken Co Ltd Coating method for exposed surface of concrete
KR100621785B1 (en) 2004-10-27 2006-09-19 (주)디피아이 홀딩스 Aqueous paint composition for preventing sticker from being adhered to wall
US7807744B2 (en) 2005-04-18 2010-10-05 Dow Corning Corporation Architectural coating compositions containing silicone resins
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JP2008179660A (en) * 2007-01-23 2008-08-07 Mitsubishi Electric Corp Coating composition, method for coating and air-conditioner
JP2010111820A (en) * 2008-11-10 2010-05-20 Iwate Industrial Research Center Water-based and water-repellent coating composition
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