JPS6127421B2 - - Google Patents
Info
- Publication number
- JPS6127421B2 JPS6127421B2 JP13362877A JP13362877A JPS6127421B2 JP S6127421 B2 JPS6127421 B2 JP S6127421B2 JP 13362877 A JP13362877 A JP 13362877A JP 13362877 A JP13362877 A JP 13362877A JP S6127421 B2 JPS6127421 B2 JP S6127421B2
- Authority
- JP
- Japan
- Prior art keywords
- cement
- emulsion
- added
- resistant
- water
- 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.)
- Expired
Links
- 238000000576 coating method Methods 0.000 claims description 37
- 239000004568 cement Substances 0.000 claims description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 239000000839 emulsion Substances 0.000 claims description 30
- 239000010426 asphalt Substances 0.000 claims description 27
- 238000002156 mixing Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 16
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 229920003002 synthetic resin Polymers 0.000 claims description 7
- 239000000057 synthetic resin Substances 0.000 claims description 7
- 229920001971 elastomer Polymers 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims 2
- 239000011248 coating agent Substances 0.000 description 35
- 238000002474 experimental method Methods 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- -1 polyoxyethylene Polymers 0.000 description 2
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BWLKKFSDKDJGDZ-UHFFFAOYSA-N [isocyanato(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(N=C=O)C1=CC=CC=C1 BWLKKFSDKDJGDZ-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- LADVLFVCTCHOAI-UHFFFAOYSA-N isocyanic acid;toluene Chemical compound N=C=O.CC1=CC=CC=C1 LADVLFVCTCHOAI-UHFFFAOYSA-N 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Aftertreatments Of Artificial And Natural Stones (AREA)
- Paints Or Removers (AREA)
Description
本発明は、コンクリート建築物に対する防水塗
装法に関する。
従来、アスフアルトを主材としてこれを乳化し
た水性エマルジヨンから成る防水塗装剤がある
が、コンクリート下地面に塗布後、その含有水分
のため塗膜の乾燥に時間がかゝり、特にコンクリ
ート表面の凹部や建造物の隅部に塗装された表面
には水が滞溜し易く乾燥に更に時間がかゝる。通
常、その塗膜の厚みは最小2〜3mmを必要とする
が、その塗布後、その表面の水分蒸発が早くその
表面に乾燥皮膜を生成して内部の水分の蒸発を妨
げる傾向があるので、極めて薄く塗布し、その乾
燥を持つてその上に塗布することを何回も繰り返
して2〜3mm以上の所要の厚さの防水塗装とする
ことを要し、その塗装作業が難儀で且つ非能率的
となる。
更に、このようにして得られたアスフアルト防
水塗層は、気温が上昇すると軟化、流動等を生じ
易い。従てこれを改良するために例えばこれにセ
メントを混ぜることが考えられるが、延伸性が乏
しくなり、振動、衝撃等により亀裂を生じ易くな
り、防水塗膜として不適となる。
本発明は、かゝる従来の防水塗装剤による防水
塗装の上記欠点を除去し、従来のようにコンクリ
ートの凹部や建造物の隅部に対応する部分にも水
が滞溜することなく防水塗装ができ、而も一度に
2〜3mm以上に塗装してもその表面に乾燥皮膜が
できないので、内部からの水分蒸発を妨げられ
ず、而も水硬性の迅速な硬化塗膜を生成し、その
塗膜は耐振動、衝撃性、耐候性等の優れたもので
ある防水塗装を提供するもので、主材であるセメ
ント混合抵抗性のあるアスフアルト水性エマルジ
ヨンに、或はこれにセメント混合抵抗性のあるゴ
ムエマルジヨン又は及び合成樹脂エマルジヨンを
添加したものに、セメントと水硬性ウレタンプレ
ポリマーとを添加し、均一に混合したものを下地
面に直接又は下地面に塗着したシート面に塗布し
たことを特徴とする。
次に本発明の実施例につき詳述する。
本発明の防水塗装に用いる主材であるセメント
混合抵抗性あるアスフアルト水性エマルジヨン
は、これにセメントを加えたとき、乳化アスフア
ルトが直ちにゲル化することなくその均一な混合
の間、乳化状態を保持する性質を有し、従来公知
の方法でつくられる。このアスフアルト水性エマ
ルジヨン中のアスフアルト分は55〜65%になるよ
うにアスフアルトと乳化剤水とを配合して製造す
る。アスフアルト分が65%以上になるとセメント
混合抵抗性が悪くなり、55%以下であると水分が
多くなりすぎ良好な塗膜形成が困難となる。
セメント混合抵抗性あるアスフアルト水性エマ
ルジヨンを得るためには、乳化剤として従来公知
のセメント混合用アスフアルト水性エマルジヨン
用乳化剤を用いることが出来る。例えばポリオキ
シエチレンアルキフエノール系の非イオン性乳化
剤、又はアルキル第4級アンモニウム系、アルキ
ルイミダゾリン系の陽イオン性乳化剤が、気温の
変化による粘度変化が少く安定していて作業性が
良好で最適である。これに混入するセメントとし
ては、普通のポルトランドセメント、早強セメン
ト、超早強セメント等が用いられる。セメントの
最大の吸水性能、即ち、水と反応硬化し硬化塗膜
の表面に遊離水が滞溜せずに硬化成形塗膜を得る
ためには、水と略同量までの添加により得られ
る。これは、通常のセメントと水との混和物の硬
化成形物を得る場合と同様である。
又該アスフアルト水性エマルジヨンに混入され
るウレタンプレポリマーは、末端水酸基2〜3個
を有する平均分子量1000〜10000のポリアルキレ
ングリコールに有機ポリイソシアネート化合物を
NCO/OH当量比2〜8で反応させて得られるも
のが適当である。(例えば商品名「ハイセル
OH−1、東邦化学工業(株)製、商品名「ポリグラ
ウト W−1」第一工業薬品(株)製)
前述したポリアルキレングリコールは公知の製
造法で調製されるもので、活性水酸基を2〜3個
有する化合物例えばプロピレングリコールジおよ
びトリプロピレングリコール、ブタンジオール、
エチレングリコール、グリセリン、トリメチロー
ルプロパン、ヒマシ油、等に、エチレンオキシド
と他の炭素数3以上のアルキレンオキシド類例え
ば、プロピレンオキシド、ブチレンオキシド、ス
チレンオキシド等を付加重合させることにより得
られる。又、有機ポリイソシアネート化合物と
は、トルエケンイソシアネート、ジフエニルメタ
ンイソシアネート、ナフタレンジイソシアネー
ト、ポリメチレンポリフエニルイソシアネート等
の芳香族系の有機ポリイソシアネート等である。
NCH/OH当量比は2〜8が好ましい。
この水硬性ポリウレタンは、最大、その重量の
約10倍の吸水性能を有し、且つその吸水に於て水
の1部と化学反応し炭酸ガスを発生して独立気泡
のゴム様乃至寒天様の弾性固化物を形成する性能
がある。
而して、本発明を実室するに当り、その混合物
の調製に当りその所定量のアスフアルト水性エマ
ルジヨン中の水分量を考慮し、これを実質上全て
吸収するに足る量のセメントと水硬性プレポリマ
ーとを混合するようにすることが好ましい。又こ
のアスフアルト水性エマルジヨンに加えゴム又は
及び合成樹脂の水性エマルジヨンを併用した場合
は、これらに含まれる水分の総和量を考慮し、こ
れに応じてセメントと水硬性プレポリマーの混合
量を増大せしめることは勿論である。その実際の
配合例により説明するに、水分約40%を含むよう
に作られたアスフアルト水性エマルジヨン100重
量部(水分40重量部)に対し、ポルトランドセメ
ント30重量部と水硬性ウレタンプレポリマー1重
量部とを添加し良く混合しこれを施工すべきコン
クリート面に流し2mm以上の均一な厚さに塗布す
る。然るときは、表面に全く遊離水の滞溜のない
良好な防水塗層が得られ、そのまゝ僅か2〜3時
間の放置で、弾性をもつ硬化防水塗膜が得られ
る。而してこの場合、従来のように、表面に乾燥
皮膜を生せず、従て内部からの水分の蒸発が良好
にでき良好均一な乾燥塗膜として得られる。上記
の配合に見るように、セメントは最大でその重量
の約100%の水を吸収する性能をもつので、その
30重量%の添加はアスフアルト水性エマルジヨン
の含有水分の約30重量%を吸収し、1方水硬性ウ
レタンプレポリマーの1重量部の添加は、その含
有水分の約10重量%の吸水を吸収し、過剰に遊離
水が生成塗膜の表面に生成されず、良好な塗装が
得られる。上記の配合の混合物は、スラリー状で
その塗布作業を容易にする。勿論、上記の水硬性
添加物の配合量を増大し或はその配合割合を適当
に変更して適当な流動性と粘性をもつ混合物とし
て使用することが出来る。
尚、更に、ゴムラテツクスや合成樹脂エマルジ
ヨンを追加配合する場合は、その追加される水分
の含量を考慮してセメント及び又は水硬性ウレタ
ンプレポリマーの添加量を増大せしめることは勿
論で、この場合は、そのゴム又は合成樹脂の添加
で、塗膜の延伸性の増大、コンクリート表面又は
防水材基材の表面に対する付着性耐候性、耐腐蝕
性等の一層の向上が得られる。
尚、前記の配合組成中には、少量の無機又は有
機繊維又はその混合繊維を添加せしめることも出
来る。
而して、発明者の試験研究によれば、アスフア
ルト水性エマルジヨンに対し、セメントだけ、或
はプレポリマーだけを混合したものを塗布しても
本発明の目的とする塗膜が得られず、両添加剤を
併用する必要があり、好ましい塗膜を得るには、
夫々その添加量に適当な範囲があることを見出し
た。次にその比較実験結果を下記表に示す。
The present invention relates to a waterproof coating method for concrete buildings. Conventionally, there are waterproof coatings made of a water-based emulsion made by emulsifying asphalt as its main material, but after being applied to the concrete base, the coating takes a long time to dry due to the moisture content, especially in the concave areas of the concrete surface. Water tends to accumulate on painted surfaces and corners of buildings, making it take longer to dry. Normally, the thickness of the coating film needs to be at least 2 to 3 mm, but after application, the water on the surface evaporates quickly and a dry film tends to form on the surface, preventing the evaporation of internal water. It is necessary to apply a very thin layer of water and then wait for it to dry before applying it over and over again to obtain a waterproof coating of 2 to 3 mm or more, making the painting process difficult and inefficient. become a target. Furthermore, the asphalt waterproof coating layer obtained in this manner tends to soften, flow, etc. when the temperature rises. Therefore, in order to improve this, for example, it is possible to mix cement into this, but the stretchability becomes poor and cracks are likely to occur due to vibrations, shocks, etc., making it unsuitable as a waterproof coating film. The present invention eliminates the above-mentioned drawbacks of waterproof coating using conventional waterproof coating agents, and enables waterproof coating without the accumulation of water in areas corresponding to concave parts of concrete or corners of buildings as in the past. Even if it is applied more than 2 to 3 mm at a time, a dry film is not formed on the surface, so moisture evaporation from the inside is not prevented, and a rapidly curing hydraulic film is produced. The coating film provides a waterproof coating with excellent vibration resistance, impact resistance, weather resistance, etc. It is made of asphalt water-based emulsion, which is the main material, and has a cement mixture resistance. Cement and hydraulic urethane prepolymer are added to a certain rubber emulsion or synthetic resin emulsion, and the mixture is uniformly applied to the base surface directly or to the sheet surface coated on the base surface. shall be. Next, examples of the present invention will be described in detail. The asphalt aqueous emulsion that is resistant to cement mixing, which is the main material used in the waterproof coating of the present invention, maintains an emulsified state during uniform mixing without immediately gelling when cement is added to the emulsified asphalt. It has properties and can be produced by conventionally known methods. This aqueous asphalt emulsion is produced by blending asphalt and emulsifier water so that the asphalt content in the asphalt aqueous emulsion is 55 to 65%. If the asphalt content exceeds 65%, the cement mixing resistance will deteriorate, and if the asphalt content exceeds 55%, there will be too much moisture, making it difficult to form a good coating film. In order to obtain an asphalt aqueous emulsion that is resistant to cement mixing, a conventionally known emulsifier for asphalt aqueous emulsion for cement mixing can be used as an emulsifier. For example, polyoxyethylene alkyphenol-based nonionic emulsifiers, or alkyl quaternary ammonium-based or alkylimidazoline-based cationic emulsifiers are optimal because they have little change in viscosity due to changes in temperature, are stable, and have good workability. be. As the cement to be mixed in, ordinary Portland cement, early strength cement, ultra early strength cement, etc. are used. In order to obtain the maximum water absorption performance of cement, that is, to obtain a cured coating film by reacting with water and curing without stagnation of free water on the surface of the cured coating film, the amount of cement to be added is approximately the same as that of water. This is similar to the case of obtaining a cured molded product of a normal mixture of cement and water. The urethane prepolymer mixed into the asphalt aqueous emulsion is a polyalkylene glycol having an average molecular weight of 1,000 to 10,000 and having 2 to 3 terminal hydroxyl groups and an organic polyisocyanate compound.
Those obtained by reacting at an NCO/OH equivalent ratio of 2 to 8 are suitable. (For example, the product name "Hicel"
OH-1, manufactured by Toho Chemical Industry Co., Ltd., trade name "Polygrout W-1" manufactured by Dai-ichi Kogyo Yakuhin Co., Ltd.) The above-mentioned polyalkylene glycol is prepared by a known manufacturing method, and has two active hydroxyl groups. Compounds having ~3 such as propylene glycol di- and tripropylene glycol, butanediol,
It can be obtained by addition polymerizing ethylene oxide and other alkylene oxides having 3 or more carbon atoms, such as propylene oxide, butylene oxide, styrene oxide, etc., to ethylene glycol, glycerin, trimethylolpropane, castor oil, etc. Further, the organic polyisocyanate compound includes aromatic organic polyisocyanates such as toluene isocyanate, diphenylmethane isocyanate, naphthalene diisocyanate, and polymethylene polyphenyl isocyanate.
The NCH/OH equivalent ratio is preferably 2 to 8. This hydraulic polyurethane has a maximum water absorption capacity of approximately 10 times its weight, and when it absorbs water, it chemically reacts with a portion of the water to generate carbon dioxide gas, forming a closed-cell rubber-like or agar-like structure. It has the ability to form elastic solidified materials. Therefore, when putting the present invention into practice, the amount of water in the predetermined amount of asphalt aqueous emulsion is taken into account when preparing the mixture, and cement and hydraulic preform are added in amounts sufficient to absorb substantially all of the water. It is preferable to mix it with a polymer. In addition, if an aqueous emulsion of rubber or synthetic resin is used in addition to this asphalt aqueous emulsion, the total amount of water contained in these should be considered and the amount of cement and hydraulic prepolymer mixed should be increased accordingly. Of course. To explain with an actual blending example, 100 parts by weight of asphalt aqueous emulsion (40 parts by weight) made to contain about 40% water, 30 parts by weight of Portland cement and 1 part by weight of hydraulic urethane prepolymer. Add and mix well, then pour this onto the concrete surface to be constructed and apply it to a uniform thickness of 2 mm or more. In such a case, a good waterproof coating layer with no accumulation of free water on the surface can be obtained, and a cured waterproof coating film with elasticity can be obtained by leaving it as it is for only 2 to 3 hours. In this case, unlike the conventional method, no dry film is formed on the surface, and therefore moisture can be evaporated from the inside well, resulting in a well-uniform dry coating film. As seen in the above formulation, cement has the ability to absorb up to approximately 100% of its weight in water;
The addition of 30% by weight will absorb about 30% of the water content of the asphalt aqueous emulsion, while the addition of 1 part by weight of hydraulic urethane prepolymer will absorb about 10% of the water content of the asphalt aqueous emulsion. Excessive free water is not generated on the surface of the coating film, resulting in a good coating. The mixture having the above formulation is in the form of a slurry, which facilitates the application process. Of course, it is possible to increase the blending amount of the above-mentioned hydraulic additive or to change the blending ratio appropriately to obtain a mixture having suitable fluidity and viscosity. Furthermore, if rubber latex or synthetic resin emulsion is additionally blended, it goes without saying that the amount of cement and/or hydraulic urethane prepolymer added should be increased in consideration of the added water content; in this case, By adding the rubber or synthetic resin, it is possible to further improve the extensibility of the coating film, the adhesion to the concrete surface or the surface of the waterproof material base material, weather resistance, corrosion resistance, etc. Incidentally, a small amount of inorganic or organic fibers or mixed fibers thereof may be added to the above-mentioned composition. According to the inventor's test research, the coating film targeted by the present invention cannot be obtained even if a mixture of only cement or only prepolymer is applied to asphalt aqueous emulsion; It is necessary to use additives in combination, and to obtain a desirable coating film,
It has been found that there is a suitable range for the amount of each added. Next, the results of the comparative experiment are shown in the table below.
【表】
上記表から明らかなように、セメントのみを添
加した場合は、実験No.1並にNo.2の数値が示すよ
うに、脆く、延伸率小さく、耐候性が不合格の硬
化塗膜や測定できない硬化不良塗膜を生じ、又水
硬性ウレタンプレポリマーのみを添加した場合
は、実験No.7、No.8の数値が示すように、硬化不
良で測定ができないか、耐水性が悪く、防水塗膜
として不適な塗膜が生成する。これに対し、本発
明のように、セメントと水硬性ウレタンプレポリ
マーを併用した場合は、実験No.3,4,5の数値
が示すように、上記のような、セメント又は水硬
性ウレタンプレポリマーを夫々単独を使用した場
合では全く得られない、引張強さ、引裂強さ、延
伸率、耐水性、耐候性(耐オゾン性)の全てに於
て基準に合格した優れた防水塗膜が得られること
が分る。
実験No.6は、耐水性でやゝ劣るが、その他の全
ての点では合格するので、他の防水基材の表面に
ラミネート層とすれば、その機械的特性、耐候性
を向上し得られる。然し乍ら、直接コンクリート
面の塗膜としては不利である。多くの実験によれ
ば、延伸率100%以下、吸水率5%以下の塗膜が
コンクリート構築物の振動、衝撃に対し強く安定
で又耐水性も強いため好ましく、このため、上記
実験No.3,4,5のように、アスフアルト水性エ
マルジヨン100重量部に対しセメント20〜30重量
部及びポリウレタンプレポリマー1〜4重量部の
範囲を配合することにより確実に優れた防水塗膜
が得られることが分つた。
尚、本発明の防水塗装は又、有機質又は無機質
の織布、不織布等のフエルト状シート、アスフア
ルト防水シート等のシートと共に形成しても良
く、この場合は、下地面に本法の上記三者混合か
ら成る防水塗装剤又は通常の任意のアスフアルト
防水剤等を塗布しその完全に硬化乃至乾燥しない
うちに前記シート材を敷設貼着し、その上に本法
防水塗装剤を塗布しその防水塗膜層を形成するよ
うにしてもよい。
このように本発明によるときは、アスフアルト
水性エマルジヨンを主材とし、これにセメントと
水硬性ウレタンプレポリマーを併用添加したもの
を被防水面に塗布するようにしたので、従来のア
スフアルト水性エマルジヨンによる塗装のよう
に、1度に2mm以上の厚さに塗布しても、容易に
乾燥すると共に短時間で自硬硬化塗膜となり、そ
の塗装施工を容易にし、又アスフアルト水性エマ
ルジヨンに、セメントのみ又は水硬性ウレタンプ
レポリマーのみを添加したものを使用した場合に
見られる硬化塗膜とならず、或は硬化塗膜となつ
ても延伸率が著しく小さく、且つ耐候性が不合格
となるような不都合な現象を生ぜずに、優れた水
硬性塗膜を得ることが出来る等の効果を有する。[Table] As is clear from the table above, when only cement was added, the cured coating film was brittle, had a low elongation rate, and failed in weather resistance, as shown by the numbers in Experiment No. 1 and No. 2. In addition, when only hydraulic urethane prepolymer was added, as shown in the values of Experiment No. 7 and No. 8, the coating film was cured poorly and could not be measured, or the water resistance was poor. , a coating film unsuitable as a waterproof coating is formed. On the other hand, when cement and hydraulic urethane prepolymer are used together as in the present invention, as shown by the numerical values of Experiment Nos. 3, 4, and 5, cement or hydraulic urethane prepolymer as described above An excellent waterproof coating film that passes the standards in terms of tensile strength, tear strength, elongation rate, water resistance, and weather resistance (ozone resistance), which cannot be obtained by using each separately, can be obtained. I know that it will happen. Experiment No. 6 is slightly inferior in water resistance, but passes in all other respects, so if a laminate layer is applied to the surface of another waterproof base material, its mechanical properties and weather resistance can be improved. . However, it is disadvantageous as a coating film directly on concrete surfaces. According to many experiments, a coating film with an elongation rate of 100% or less and a water absorption rate of 5% or less is preferable because it is strong and stable against vibrations and impacts of concrete structures, and has strong water resistance. 4 and 5, it has been found that an excellent waterproof coating film can be reliably obtained by blending 20 to 30 parts by weight of cement and 1 to 4 parts by weight of polyurethane prepolymer to 100 parts by weight of asphalt aqueous emulsion. Ivy. The waterproof coating of the present invention may also be formed with sheets such as organic or inorganic woven fabrics, nonwoven fabrics, felt sheets, asphalt waterproof sheets, etc. In this case, the above-mentioned three materials of the present method may be applied to the base surface. A waterproof coating agent consisting of a mixture or any ordinary asphalt waterproofing agent, etc. is applied, and the sheet material is laid and adhered before it completely hardens or dries, and the waterproof coating agent of this method is applied on top of that. A film layer may also be formed. In this way, according to the present invention, the asphalt water-based emulsion is used as the main material, and a mixture of cement and hydraulic urethane prepolymer is applied to the surface to be waterproofed. Even if applied to a thickness of 2 mm or more at a time, it dries easily and becomes a self-hardening coating in a short time, making it easy to apply. There are disadvantages such as the case where a hard urethane prepolymer alone is used, resulting in a hardened coating film, or even if a cured coating film is formed, the stretching ratio is extremely small and the weather resistance is rejected. It has the effect of being able to obtain an excellent hydraulic coating film without causing any phenomenon.
Claims (1)
アルト水性エマルジヨンに、或はこれにセメント
混合抵抗性のあるゴムエマルジヨン又は及び合成
樹脂エマルジヨンを添加したものに、セメントと
水硬化性ウレタンプレポリマーとを添加し、均一
に混合したものを下地面に直接又は下地面に塗着
したシート面に塗布したことを特徴とする防水塗
装法。 2 主材であるセメント混合抵抗性のあるアスフ
アルト水性エマルジヨンに、或はこれにセメント
混合抵抗性のあるゴムエマルジヨン又は及び合成
樹脂エマルジヨンを添加したものに、セメントと
水硬性ウレタンプレポリマーとを前記エマルジヨ
ン中の水分を実質上全部吸収するに足る量を添加
し、均一に混合したものを下地面に直接又は下地
面に塗着したシート面に塗布したことを特徴とす
る特許請求の範囲1に記載の防水塗装法。 3 主材であるセメント混合抵抗性のあるアスフ
アルト水性エマルジヨンに、或はこれにセメント
混合抵抗性のあるエマルジヨン又は及び合成樹脂
エマルジヨンを添加したものに、該セメント混合
抵抗性エマルジヨン100重量部に対して、ポルト
ラン系セメント20〜30重量部と、水硬性ウレタン
プレポリマー1〜4重量部とを添加し均一に混合
したものを下地面に直接又は下地に塗着したシー
ト面に塗布したことを特徴とする特許請求の範囲
1に記載の防水塗装法。[Scope of Claims] 1. Cement and water-curing urethane are added to the main material, an asphalt aqueous emulsion that is resistant to cement mixing, or to which is added a rubber emulsion or a synthetic resin emulsion that is resistant to cement mixing. A waterproof coating method characterized by adding a prepolymer and applying a uniform mixture to the base surface directly or to a sheet surface coated on the base surface. 2. Cement and hydraulic urethane prepolymer are added to the main material, an asphalt aqueous emulsion that is resistant to cement mixing, or to which is added a rubber emulsion or a synthetic resin emulsion that is resistant to cement mixing. Claim 1, characterized in that the mixture is added in an amount sufficient to absorb substantially all of the moisture, and a uniformly mixed mixture is applied directly to the base surface or to a sheet surface coated on the base surface. Waterproof coating method. 3. To the asphalt water-based emulsion that is resistant to cement mixing, which is the main material, or to which an emulsion that is resistant to cement mixing or a synthetic resin emulsion is added, based on 100 parts by weight of the emulsion that is resistant to cement mixing. , characterized in that 20 to 30 parts by weight of Portolan cement and 1 to 4 parts by weight of hydraulic urethane prepolymer are added and mixed uniformly and applied directly to the substrate surface or to the sheet surface coated on the substrate. The waterproof coating method according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13362877A JPS5466938A (en) | 1977-11-09 | 1977-11-09 | Water proof coating and material therefor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13362877A JPS5466938A (en) | 1977-11-09 | 1977-11-09 | Water proof coating and material therefor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5466938A JPS5466938A (en) | 1979-05-29 |
JPS6127421B2 true JPS6127421B2 (en) | 1986-06-25 |
Family
ID=15109254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13362877A Granted JPS5466938A (en) | 1977-11-09 | 1977-11-09 | Water proof coating and material therefor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5466938A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5716070A (en) * | 1980-07-04 | 1982-01-27 | Nippon Oil & Fats Co Ltd | Composition for water-proofing coat |
JPS58144186A (en) * | 1982-02-18 | 1983-08-27 | ジェイエスアール株式会社 | Room temperature waterproofing method |
-
1977
- 1977-11-09 JP JP13362877A patent/JPS5466938A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5466938A (en) | 1979-05-29 |
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