JPS5920702B2 - Leak prevention agent - Google Patents

Leak prevention agent

Info

Publication number
JPS5920702B2
JPS5920702B2 JP51151465A JP15146576A JPS5920702B2 JP S5920702 B2 JPS5920702 B2 JP S5920702B2 JP 51151465 A JP51151465 A JP 51151465A JP 15146576 A JP15146576 A JP 15146576A JP S5920702 B2 JPS5920702 B2 JP S5920702B2
Authority
JP
Japan
Prior art keywords
weight
water
latex emulsion
urethane prepolymer
resin
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
Application number
JP51151465A
Other languages
Japanese (ja)
Other versions
JPS5377250A (en
Inventor
信輔 紀藤
伸夫 東條
正彦 石田
道昭 飛田
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.)
Taiho Kogyo Co Ltd
Original Assignee
Taiho Kogyo 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 Taiho Kogyo Co Ltd filed Critical Taiho Kogyo Co Ltd
Priority to JP51151465A priority Critical patent/JPS5920702B2/en
Publication of JPS5377250A publication Critical patent/JPS5377250A/en
Publication of JPS5920702B2 publication Critical patent/JPS5920702B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Polyurethanes Or Polyureas (AREA)
  • Sealing Material Composition (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 本発明は工業排水、下水道、工業用水、農業用水など主
に水を通す管材の接合部に使用する漏水防止剤に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a water leakage prevention agent that is used at the joints of pipe materials that mainly pass water such as industrial wastewater, sewerage systems, industrial water, and agricultural water.

周知の様に上記目的の管材としては例えばヒユーム管、
コンクリート管などがあり、適宜の長さの管材を順次接
合して長尺なものとし、内部に水を通すのである。
As is well known, examples of pipe materials for the above purpose include Huyum pipes,
There are concrete pipes, etc., and pipes of appropriate length are successively joined to make a long pipe, and water is passed inside.

したがつて水の通路には多数の接合部が有り、各接合部
は確実に封水しないと漏水の危険が有る。
Therefore, there are many joints in the water passage, and there is a risk of water leakage if each joint is not reliably sealed.

従来の管材の接合部の封水手段としては、接合部にアス
ファルトを充填したり、或いは合成樹脂や合成ゴム質の
シート材若しくは環材を接合部に介在したり、外周面を
バンド締めしたり、又は上記各手段を適宜に組合せたり
化学剤を充填している。しかし、いずれの手段も完成さ
れたものではなく、何等かの欠点が有る。
Conventional water sealing methods for joints of pipe materials include filling the joint with asphalt, interposing a synthetic resin or synthetic rubber sheet or ring material in the joint, or tightening the outer circumferential surface with a band. , or by appropriately combining the above-mentioned means or filling the container with a chemical agent. However, none of these methods is perfect and has some drawbacks.

この欠患としては封水効果が確実でなくて長期間経過す
ると地盤変動やずれにより漏水が生じたり、接合部にお
ける封水作業が面倒なため多数の接合部を封水処理する
のに多くの人間と期間を要したり、低価格で供すること
ができないこと等である。これらの欠点を解消する手段
としては特開昭49−125924号公報で示すように
、管材の一端のベル部に他の管材の他端のスピゴツト部
を嵌着して接続するいんろう型継手において、あらかじ
めNCO10Hのモル比を1.0〜2.0の基に反応さ
せたプレポリマー又はこれと充填剤との混合物をベル部
とスピゴツト部で囲まれる内部にパッキングとともに充
填する方法である。
These deficiencies include the fact that the water sealing effect is not reliable, and after a long period of time, water leaks may occur due to ground movement or displacement, and the sealing work at joints is troublesome, so it takes a lot of time to seal many joints. These include the fact that it requires time and human resources, and that it cannot be provided at a low price. As a means to solve these drawbacks, as shown in Japanese Patent Application Laid-Open No. 49-125924, there is a spigot type joint in which a bell part at one end of a pipe material is fitted into a spigot part at the other end of another pipe material. This is a method in which a prepolymer or a mixture of the prepolymer and a filler, which has been reacted in advance with a NCO10H molar ratio of 1.0 to 2.0, is packed together with packing into the interior surrounded by the bell part and the spigot part.

この方法によればプレポリマーに含有する遊離・ のN
CO基が水和重合を生じ、炭酸ガスを発生して高分子の
発泡膨張弾性質となり、上記したベル部とスピゴット部
との間に充満して封水効果を高め、漏水を防止するので
ある。
According to this method, free N contained in the prepolymer
The CO group undergoes hydration polymerization, generates carbon dioxide gas, and the polymer expands and becomes elastic, filling the space between the bell section and the spigot section, enhancing the water sealing effect and preventing water leakage. .

しかしこの方法であつても、プレポリマーの硬・ 化時
間が短かいので作業が困難で、コンクリートに対する接
着性が乏しいばかりでなく発泡質が緻密でないから衝撃
などによる物理的要因で変化しコーやすいので十分な封
水効果を期待できず、しかも内部に存在する気泡の径が
大きくなるので長期間の経過で破壊して漏水する危険が
ある。
However, even with this method, it is difficult to work because the prepolymer has a short curing time, and not only does it have poor adhesion to concrete, but the foam is not dense and is susceptible to change due to physical factors such as impact. Therefore, a sufficient water sealing effect cannot be expected, and furthermore, since the diameter of the bubbles existing inside becomes large, there is a risk that they will break and leak water over a long period of time.

本発明者等は上記の欠点を解消すべく研究の結果、本発
明の完成に達したもので、その要旨とするところはイソ
シアネートとポリオールとの反応生成物であつて末端基
に遊離のイソシアネート基を有する水硬性ウレタンプレ
ポリマ一と樹脂ラテツクスエマルジヨンとを混合させ、
該混合物を管材の接合部に充填して発泡質を形成させる
ようにしたことにある。
The present inventors have completed the present invention as a result of research to eliminate the above-mentioned drawbacks. Mixing a hydraulic urethane prepolymer with a resin latex emulsion,
The present invention is characterized in that the mixture is filled into the joints of the pipe materials to form a foamed material.

イソシアネート基を有するウレタンブレポリマ一と樹脂
ラテツクスエマルジヨンとを混合すると、プレポリマ一
と樹脂ラテツクスエマルジヨンに含む水成分との縮合反
応によつて生じる発泡質の内部に樹脂成分が分散して混
入し、樹脂成分が骨材的な作用を生じるので十分な弾性
をもたらせる。
When the urethane polymer having isocyanate groups and the resin latex emulsion are mixed, the resin component is dispersed inside the foam produced by the condensation reaction between the prepolymer and the water component contained in the resin latex emulsion. The resin component acts like an aggregate, providing sufficient elasticity.

したがつて管材の接合部において十分な封水効果をもた
らせることができる。本発明で使用するイソシアネート
としてはトリレン・ジイソシアネート、ナフタレン・1
・5・ジイソシアネート、エチレン・ジイソシアネート
、トリメチレン・ジイソシアネート、テトラメチレン・
ジイソシアネート、ペンタメチレン・ジイソシアネート
、ヘキサメチレン・ジイソシアネート、ヘプタメチレン
・ジイソシアネート、フエニレン・ジイソシアネート、
トルイレン・ジイソシアネートなど2個のイソシアネー
ト基を有するものである。
Therefore, a sufficient water sealing effect can be achieved at the joints of the pipe materials. The isocyanates used in the present invention include tolylene diisocyanate and naphthalene diisocyanate.
・5. Diisocyanate, ethylene diisocyanate, trimethylene diisocyanate, tetramethylene ・
Diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, heptamethylene diisocyanate, phenylene diisocyanate,
It has two isocyanate groups, such as toluylene diisocyanate.

又、本発明で使用するポリオールとしては、エチレング
リコール、ポリエチレングリコール、ビスフエノールジ
オキシエチルエーテル、ビスフエノールジオキシプロピ
ルエーテル、ネオペンチルグリコールなどのジオールな
どであつて、これらを適宜に選択して組み合せることに
より性質が異なつた多種の反応生成物とすることができ
る。
In addition, the polyols used in the present invention include diols such as ethylene glycol, polyethylene glycol, bisphenol dioxyethyl ether, bisphenol dioxypropyl ether, and neopentyl glycol, and these may be appropriately selected and combined. By doing so, a wide variety of reaction products with different properties can be obtained.

そして、本発明によれば水硬性ウレタンプレポリマ一は
、NCO/0Hのモル比が3.0〜7.0の範囲のもの
のイソシアネートとポリオールの反応生成物であること
が望ましい。即ちNCO/0Hの比率が3,0以下であ
れば反応生成物に含まれるNCOの含有量が少くなり、
水和反応による発泡倍率が小さくなる。
According to the present invention, the hydraulic urethane prepolymer is preferably a reaction product of an isocyanate and a polyol having an NCO/OH molar ratio in the range of 3.0 to 7.0. That is, if the ratio of NCO/0H is 3.0 or less, the content of NCO contained in the reaction product will be reduced,
The foaming ratio due to hydration reaction becomes smaller.

したがつて水和反応の結果によつて生じる膨張率が小さ
くなり、十分な弾性特性を備えた発泡質とならない。一
方、NCO/0Hの比率が7.0以上であれば、反応生
成物は低分子量のもの、即ち縮合度の小さいブレポリマ
一であつて、遊離のイソシアネート基が多く存在する。
したがつて水和反応によつて発泡した場合、各気泡の総
容積が著しく大きくなり、漏水防止剤としての物理的強
度を有しなかつたり或いは水和反応により生じるCO2
を混合物の内部に閉じこめておくことができず、外部に
放出して発泡質とならない。
Therefore, the expansion rate caused by the hydration reaction becomes small, and the foam does not have sufficient elastic properties. On the other hand, if the NCO/OH ratio is 7.0 or more, the reaction product is of low molecular weight, ie, a bleed polymer with a low degree of condensation, and contains many free isocyanate groups.
Therefore, when foaming occurs due to the hydration reaction, the total volume of each bubble increases significantly, and the CO2 generated by the hydration reaction may not have the physical strength as a water leakage preventive agent.
cannot be trapped inside the mixture, and cannot be released to the outside to form a foamy substance.

上記したように、NCO/0Hのモル比が3.0〜7.
0の範囲であるイソシアネートとポリオールとの反応生
成物である水硬性ウレタンプレポリマ一はそのまXでも
使用できるが、溶剤に希釈して取り扱いやすく、樹脂ラ
テツクスエマルジヨンと混合しやすい状態に粘度を調整
して使用するのが好ましい。
As mentioned above, the molar ratio of NCO/OH is 3.0 to 7.
Hydraulic urethane prepolymer 1, which is a reaction product of polyol and isocyanate in the range of It is preferable to adjust and use it.

このような溶剤としては、上記プレポリマ一を溶解させ
ることができ、揮発性であり、しかもプレポリマ一に含
有する遊離のイソシアネート基と反応しないものであれ
ばどのようなものでもよいが、例えばメチルエチルケト
ン、アセトン、メチルイソブチルケトン、ベンゼン、ト
ルエン、キシレンなどを利用することができる。
Any solvent may be used as long as it can dissolve the prepolymer, is volatile, and does not react with free isocyanate groups contained in the prepolymer, such as methyl ethyl ketone, Acetone, methyl isobutyl ketone, benzene, toluene, xylene, etc. can be used.

上記した水硬性ウレタンプレポリマ一に混合する樹脂ラ
テツクスエマルジヨンとしては酢酸ビニルエマルジヨン
、塩化ビニルエマルジヨン、アクリルエマルジヨン、エ
ポキシエマルジヨン、スチレンブタジエンラテツクス、
塩化ビニリデンデイスパージヨン、アルキツドエマルジ
ヨン、アクリルアルキツドエマルジヨン、アスフアルト
エマルジヨン等ゴム成分等を含有するものであつて、こ
れらの樹脂ラテツクスエマルジヨンのうちではスチレン
ブタジエンラテツクスが特に有効に使用することができ
る。
Examples of the resin latex emulsion to be mixed with the above-mentioned hydraulic urethane prepolymer include vinyl acetate emulsion, vinyl chloride emulsion, acrylic emulsion, epoxy emulsion, styrene-butadiene latex,
Among these resin latex emulsions, styrene-butadiene latex is particularly effective. can be used.

また樹脂ラテツクスエマルジヨンにおける樹脂成分含有
量は25〜70重量%が望ましく、25重量%以下であ
れば樹脂成分による効果が表われず、70重量%以上で
あれば安定性、取扱上において不利になる。更にウレタ
ンプレポリマ一と樹脂ラテツクスエマルジヨンとの混合
率にも影響されるが、樹脂成分の量が多ければ生成する
弾性発泡質にも悪影響を与える。
In addition, the content of the resin component in the resin latex emulsion is preferably 25 to 70% by weight; if it is less than 25% by weight, the effect of the resin component will not appear, and if it is more than 70% by weight, it will be disadvantageous in terms of stability and handling. become. Furthermore, although it is influenced by the mixing ratio of the urethane prepolymer and the resin latex emulsion, if the amount of the resin component is too large, the quality of the elastic foam produced will be adversely affected.

例えばウレタンプレポリマ一1重量部に対して水成分が
0,5〜4重量部であつて、樹脂成分が0.1〜2重量
部であれば好ましく、ウレタンプレポリマ一1重量部に
対して水成分が0.7〜1.5重量部、樹脂成分が0.
3〜1.0重量部であれば更に好ましい結果を与えるこ
とができる。例え (ば樹脂成分50重量%の樹脂ラテ
ツクスエマルジヨンを用いるとすれば、ウレタンポリマ
ー1重量部に対して約0.25〜3重量部の混合が適し
ている。上記した各条件によつて遊離のイソシアネート
基を有する水硬性ウレタンプレポリマ一と樹脂分散水溶
液とを混合すると、ウレタンプレポリマ一に含有する遊
離のイソシアネート基が樹脂ラテツクスエマルジヨンの
水成分と縮合反応し、その結果CO2を放出して弾性有
る発泡質となる。
For example, it is preferable that the water component is 0.5 to 4 parts by weight per 1 part by weight of the urethane prepolymer, and the resin component is 0.1 to 2 parts by weight. The water component is 0.7 to 1.5 parts by weight, and the resin component is 0.7 to 1.5 parts by weight.
More preferable results can be obtained if the amount is 3 to 1.0 parts by weight. For example, if a resin latex emulsion containing 50% by weight of the resin component is used, it is suitable to mix about 0.25 to 3 parts by weight per 1 part by weight of the urethane polymer. When a hydraulic urethane prepolymer having free isocyanate groups is mixed with an aqueous resin dispersion solution, the free isocyanate groups contained in the urethane prepolymer undergo a condensation reaction with the water component of the resin latex emulsion, resulting in the production of CO2. When released, it becomes an elastic foam.

この場合、樹脂ラテツクスエマルジヨンの分散質である
樹脂成分は発泡質の内部に均一な分散状態で混入して骨
材としての機能を有し、無機質骨材には生じない弾性を
具備する。またコンクリート等に対して接着性が著しく
良好で、しかも樹脂成分によつてイソシアネート基によ
る局部的な急激発泡を抑制することができ、気泡が均一
に分散してしかも緻密な発泡質となる。更にウレタンプ
レポリマ一と樹脂ラテツクスエマルジヨンとを混合した
とき、発泡質の生成反応は適当に緩慢であるから発泡質
の硬化が遅延し、管材の接合部における作業時に扱い易
く、作業能率を高めることができる。
In this case, the resin component, which is the dispersoid of the resin latex emulsion, is mixed in a uniformly dispersed state inside the foam and functions as an aggregate, providing elasticity that does not occur in inorganic aggregates. In addition, it has extremely good adhesion to concrete and the like, and the resin component can suppress localized rapid foaming due to isocyanate groups, resulting in a dense foam with uniformly dispersed air bubbles. Furthermore, when the urethane prepolymer and the resin latex emulsion are mixed, the foam formation reaction is appropriately slow, so the curing of the foam is delayed, making it easier to handle when working at the joints of pipe materials, and improving work efficiency. can be increased.

しかも本発明による弾性有る発泡質はウレタンプレポリ
マ一と水、又はウレタンプレポリマ一と水と無機質の骨
材とからなる発泡質と比較すると、接着力や弾性力が著
しく高くなる。更には発泡質に樹脂成分を含まなければ
収縮するが、本発明のように適宜の量の樹脂成分を含有
させることで長期間経過したとしても収縮することがな
く、特にコンクリート質の管材の漏水防止剤として著し
い効果を有する。次に本発明の漏水防止剤を使用して管
材を接続する方法を図面の実施例に基いて説明する。
Furthermore, the elastic foam according to the present invention has significantly higher adhesive strength and elasticity than foams made of a urethane prepolymer and water, or a urethane prepolymer, water, and an inorganic aggregate. Furthermore, if the foam does not contain a resin component, it will shrink, but by including an appropriate amount of resin component as in the present invention, it will not shrink even after a long period of time, and it will especially prevent water leakage from concrete pipe materials. It has remarkable effects as an inhibitor. Next, a method for connecting pipe materials using the water leakage preventive agent of the present invention will be described based on examples shown in the drawings.

管材1の一端のスピゴツト部2に他の管材1″の他端の
ベル部3を嵌め込んで環状の間隔部4を構成し、該間隔
部4の外側開口部分を合成ゴム、合成樹脂などからなる
リング材5で封じる。又、上記間隔部4の内側開口部分
は複数本の小管6・・・・・・を設けたシール材7で封
じて間隔部4を密に閉塞′し、最下端の小管61を漏水
防止剤の注入用、最上端の小管62を内気放出用、その
他の小管6・・・・・・を注入確認用とする。
The bell portion 3 at the other end of another tube 1'' is fitted into the spigot portion 2 at one end of the tube 1 to form an annular gap 4, and the outer opening portion of the gap 4 is made of synthetic rubber, synthetic resin, etc. The inner opening of the spacer 4 is sealed with a sealing member 7 provided with a plurality of small tubes 6 to tightly close the spacer 4. The small tube 61 is used for injecting the water leakage prevention agent, the small tube 62 at the top end is used for releasing internal air, and the other small tubes 6 are used for confirming injection.

なお各小管6は透明ビニールで作成するのが望ましく、
また小管61はシール材7の近くに開口させ、小管62
はリング材5の近くに開口させるのが好ましい。一方、
イソシアネートとポリオールとの反応生成物であつて末
端基に遊離のイソシアネート基を有する水硬性ウレタン
プレポリマ一の溶液槽8と樹脂ラテツクスエマルジヨン
の溶液槽9とを各々供給管10,11によつて混合器1
2に連結し、該混合器12と小管61とを接続管13で
連結する。
It is preferable that each small tube 6 be made of transparent vinyl.
In addition, the small tube 61 is opened near the sealing material 7, and the small tube 62
is preferably opened near the ring material 5. on the other hand,
A solution tank 8 for a hydraulic urethane prepolymer, which is a reaction product of an isocyanate and a polyol and has a free isocyanate group at the terminal group, and a solution tank 9 for a resin latex emulsion are connected to supply pipes 10 and 11, respectively. Mixer 1
2, and the mixer 12 and the small tube 61 are connected by a connecting tube 13.

そして溶液槽8からは水硬性ウレタンブレポリマ一の溶
液を所望量宛混合器12に圧送し、同時に溶液槽9から
は樹脂ラテツクスエマルジヨン溶液を混合器12に圧送
すれば、混合器12では両溶液が混合して接続管13か
ら小管61を通つて間隔部4に下から注入される。
Then, from the solution tank 8, a solution of hydraulic urethane polymer in a desired amount is pumped to the mixer 12, and at the same time, from the solution tank 9, the resin latex emulsion solution is pumped to the mixer 12. Both solutions are mixed and injected into the spacer 4 from below through the connecting tube 13 and the small tube 61.

上記混合物が間隔部4に次第に注入されると確認用小管
6から流出するので、混合物が流出した小管6を順次止
具(針金、バンド、クリツプ等)で閉塞し、混合物の流
出を止める。
When the mixture is gradually injected into the space 4, it flows out from the confirmation small tube 6, so the small tubes 6 through which the mixture has flowed out are sequentially closed with stoppers (wires, bands, clips, etc.) to stop the mixture from flowing out.

混合物が小管62から流出を開始したとき、混合器12
から間隔部4に混合物を供給するのを止めてそのまX養
生する。
When the mixture begins to flow out of the small tube 62, the mixer 12
From then on, the supply of the mixture to the space 4 is stopped and the X-curing is continued.

養生によつて間隔部4内の混合物が発泡質となつた頃に
シール材5及び各小管6・・・・・・を抜き取る。
When the mixture in the spacer 4 becomes foamy due to curing, the sealing material 5 and each of the small tubes 6 are removed.

これにより間隔部4には弾性有る発泡質が充填され、両
管材1,1′の接合部分を密に封じるのである。なお本
発明は上記したスピゴツト部とベル部とを有する管材に
限らず、他のどのような接続構造の管材にも実施するこ
とができ、また管材も円管ばかりでなく断面が矩形、U
字形など接合部を密に封じることができればどのような
形状のものでもよい。
As a result, the spacing portion 4 is filled with elastic foam, and the joint portion between the two tubes 1 and 1' is tightly sealed. Note that the present invention is not limited to the pipe material having the above-mentioned spigot part and bell part, but can be applied to pipe materials having any other connection structure, and the pipe material is not limited to circular pipes, but also has rectangular cross sections, U-shaped pipes, etc.
It may have any shape, such as a letter shape, as long as it can tightly seal the joint.

以下に本発明の実施例を記載する。Examples of the present invention are described below.

実施例 1 トリレンジイソシアネートとポリエチレングリコールと
をNCO/0Hのモル比が6.5となるように反応させ
た分子量約6000のウレタンプレポリマ一を、メチル
エチルケトン及びトルエンで希釈して粘度2000CP
S/20℃の溶液(第1液)とした。
Example 1 A urethane prepolymer having a molecular weight of about 6,000 made by reacting tolylene diisocyanate and polyethylene glycol so that the NCO/OH molar ratio was 6.5 was diluted with methyl ethyl ketone and toluene to obtain a viscosity of 2,000 CP.
A solution (first solution) was prepared at S/20°C.

一方、樹脂成分含有量が60重量%のスチレンブタジエ
ンラテツクス溶液(第2液)を準備し、第1液と第2液
とを第1図、第2図で示すような手段によつてポンプで
送り出し、途中の混合器で混合してヒユーム管の接合部
に充填した。
On the other hand, a styrene-butadiene latex solution (second liquid) having a resin component content of 60% by weight is prepared, and the first liquid and the second liquid are pumped by the means shown in FIGS. 1 and 2. The mixture was sent out using a mixer, mixed in an intermediate mixer, and filled into the joint of the Huum tube.

第1液と第2液の混合率は、第1液1重量部に対して第
2液1重量部、2重量部、4重量部の3種類として個々
に実施し、また上記とは別に第2液に水を使用して比較
例として各々試験をした。
The mixing ratio of the first liquid and the second liquid is 1 part by weight of the first liquid to 1 part by weight, 2 parts by weight, and 4 parts by weight of the second liquid. Each test was conducted as a comparative example using water as the second liquid.

試験方法はヒユーム管の接合部に混合物を充填して60
分経過後にヒユーム管の内部に通水し、(1)通水試験
、及轄1水圧1kg/Crll保持のま入接合部の屈曲
試験である。その結果は下記の如くである。
The test method is to fill the joint of the humid tube with the mixture and
After a minute had passed, water was passed through the inside of the humid pipe, and (1) water flow test was conducted, followed by a bending test of the internal joint while maintaining a water pressure of 1 kg/Crll. The results are as follows.

実施例 2 トリメチレンジイソシアネートとビスフエノールジオキ
シエチルエーテルとをNCO/0Hのモル比が3.5と
なるように反応させてなるウレタンプレポリマ一を、メ
チルイソブチルケトンに希釈して粘度1000CPS/
20℃の溶液(第1液)とした。
Example 2 A urethane prepolymer prepared by reacting trimethylene diisocyanate and bisphenol dioxyethyl ether such that the molar ratio of NCO/OH was 3.5 was diluted with methyl isobutyl ketone to obtain a viscosity of 1000 CPS/
A solution (first solution) was prepared at 20°C.

一方、樹脂成分含有量35重量%のスチレンプタジエン
ラテツクス溶液(第2液)を準備し、第1液1重量部に
対して第2液を2重量部とし、管材の接合部に充填した
On the other hand, a styrene-ptadiene latex solution (second liquid) having a resin component content of 35% by weight was prepared, and the second liquid was 2 parts by weight per 1 part by weight of the first liquid, and the mixture was filled into the joint of the pipe material. .

なお充填方法及び試験方法は前記実施例1と同様である
The filling method and testing method were the same as in Example 1 above.

試験結果は、(1》水圧試験が5kg/CF7lまで異
常なし、(4屈曲試験が約3試の傾きで異常なく、十分
に効果有ることが認められた。
The test results were as follows: (1) Water pressure test showed no abnormalities up to 5 kg/CF7l, (4 bending tests showed no abnormalities at approximately 3 inclinations, and it was recognized that the product was sufficiently effective.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は本発明の漏水防止剤によつて管材の接合部を封水
する方法の実施例を示す概略図で、第1図は縦断正面図
、第2図は縦断側面図である。
The drawings are schematic diagrams showing an embodiment of a method for sealing joints of pipe materials with the water leakage prevention agent of the present invention, and FIG. 1 is a longitudinal sectional front view, and FIG. 2 is a longitudinal sectional side view.

Claims (1)

【特許請求の範囲】 1 NCO/OHのモル比が3.0〜7.0の範囲内で
のイソシアネートとポリオールとの反応生成物であつて
末端基に遊離のイソシアネート基を有する水硬性ウレタ
ンプレポリマーと、樹脂ラテックスエマルジョンとから
なり、上記水硬性ウレタンプレポリマーと樹脂ラテック
スエマルジョンとは作業時に混合して使用することを特
徴とする漏水防止剤。 2 水硬性ウレタンプレポリマーと樹脂ラテックスエマ
ルジョンとを、水硬性ウレタンプレポリマーが1重量部
に対して樹脂ラテックスエマルジョンの樹脂分が0.1
〜2重量部となるように混合する特許請求の範囲第1項
記載の漏水防止剤。
[Scope of Claims] 1. A hydraulic urethane preform which is a reaction product of an isocyanate and a polyol with an NCO/OH molar ratio within the range of 3.0 to 7.0 and has a free isocyanate group at the terminal group. A water leak prevention agent comprising a polymer and a resin latex emulsion, wherein the hydraulic urethane prepolymer and the resin latex emulsion are used by mixing during work. 2 The hydraulic urethane prepolymer and the resin latex emulsion are mixed so that the resin content of the resin latex emulsion is 0.1 part by weight of the hydraulic urethane prepolymer.
The water leakage preventive agent according to claim 1, which is mixed in an amount of up to 2 parts by weight.
JP51151465A 1976-12-18 1976-12-18 Leak prevention agent Expired JPS5920702B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51151465A JPS5920702B2 (en) 1976-12-18 1976-12-18 Leak prevention agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51151465A JPS5920702B2 (en) 1976-12-18 1976-12-18 Leak prevention agent

Publications (2)

Publication Number Publication Date
JPS5377250A JPS5377250A (en) 1978-07-08
JPS5920702B2 true JPS5920702B2 (en) 1984-05-15

Family

ID=15519117

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51151465A Expired JPS5920702B2 (en) 1976-12-18 1976-12-18 Leak prevention agent

Country Status (1)

Country Link
JP (1) JPS5920702B2 (en)

Also Published As

Publication number Publication date
JPS5377250A (en) 1978-07-08

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