JPS58108232A - Water-stopping material - Google Patents

Water-stopping material

Info

Publication number
JPS58108232A
JPS58108232A JP20526481A JP20526481A JPS58108232A JP S58108232 A JPS58108232 A JP S58108232A JP 20526481 A JP20526481 A JP 20526481A JP 20526481 A JP20526481 A JP 20526481A JP S58108232 A JPS58108232 A JP S58108232A
Authority
JP
Japan
Prior art keywords
water
foam
hydrogel
hydrophilic additive
weight
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
JP20526481A
Other languages
Japanese (ja)
Inventor
Atsushi Tsutsumi
淳 堤
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.)
NHK Spring Co Ltd
Original Assignee
NHK Spring 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 NHK Spring Co Ltd filed Critical NHK Spring Co Ltd
Priority to JP20526481A priority Critical patent/JPS58108232A/en
Publication of JPS58108232A publication Critical patent/JPS58108232A/en
Pending legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

PURPOSE:To obtain a water-stopping material having improved water-stopping effect, by adding specific amounts of hydrogel and a hydrophilic additive to a foamed article, thereby increasing the permeation of water to the foamed article. CONSTITUTION:A foamed article (e.g. polyurethane resin) is incorporated with (A) 4-109wt% hydrogel, i.e. a water-insoluble water-absorbing resin powder (e.g. crosslinked sodium polyacrylate) and (B) 4-116wt% hydrophilic filler (e.g. starch, glass powder, etc.). The amount of the component (B) is >=1/10 of the component (A), and the sum of the components (A) and (B) is <=120wt%. It is preferable to foam the resin after the addition of the components (A) and (B).

Description

【発明の詳細な説明】 本発明は止水材、特に水不溶性の吸水性樹脂(以下ヒド
ロゲルと言う]粉末を含有させた発泡体からなる止水材
の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a water-stopping material, particularly a water-stopping material made of a foam containing a water-insoluble water-absorbing resin (hereinafter referred to as "hydrogel") powder.

従来、ポリウレタンの製造に際し、ヒドロゲルを加えて
、親水性、吸水性の発泡体を製造することは、広く知ら
れている。
BACKGROUND ART Conventionally, it has been widely known to add hydrogel to produce a hydrophilic, water-absorbing foam when producing polyurethane.

本発明者らはさきに、これらの親水性、吸水性の発泡体
を止木材として利用する技術を開発した。
The present inventors have previously developed a technique for utilizing these hydrophilic and water-absorbing foams as a stopper.

これらの止木材は同等の密度を有する発泡体からなる止
木材に比べて数段優れた止水性を有しているが、更に研
究の結果、更に止水能を高めることができた。
These stoppers have water-stopping properties that are much better than those made of foam having the same density, but as a result of further research, it was possible to further improve the water-stopping ability.

ヒドロゲルを含有する発泡体の止水性は、ヒドロゲルの
水保持力と膨潤力とに起因するので、止水材中に含まれ
る全てのヒドロゲルに水分が均等に浸透した状態で最大
の力を発揮する。ところがこのヒドロゲルの水保持力は
非常に強く、例えばjcII幅にヒドロゲルを密につめ
て、その片側に水をつけると、水はヒドロゲルを徐々に
伝わっていくが、その浸透速度は2cm /月程度であ
る。発泡体中に含まれた場合にも、先に水と接触する外
側部分が水を含んで膨潤し、内部には水は伝わ9@いの
で、理論的には可能な止水力が実際には発揮されない。
The water-stopping properties of foams containing hydrogels are due to the water retention and swelling power of the hydrogels, so maximum strength is exerted when all the hydrogels contained in the water-stopping material are evenly penetrated by water. . However, the water retention power of this hydrogel is very strong. For example, if the hydrogel is densely packed into a jcII width and water is applied to one side, the water will gradually travel through the hydrogel, but the permeation rate is about 2 cm / month. It is. Even when it is contained in a foam, the outer part that comes into contact with water first absorbs water and swells, and the water is transmitted to the inside, so the water stopping power that is theoretically possible does not actually work. Not demonstrated.

通常このような止水材は片面に粘着層を設けてシーリン
グ面に貼抄付けて、これを反対側のシーリング面に押し
つけて密着させて使用する。この場合、止水材の圧縮硬
さが低いと、粘着層を設けていがい止木材面とシーリン
グ面との間を水が通り抜けてしまう。
Usually, such a water-stopping material is used by providing an adhesive layer on one side and pasting it on the sealing surface, and then pressing it against the sealing surface on the opposite side to bring it into close contact. In this case, if the compressive hardness of the water stop material is low, water will pass through between the water stop material surface and the sealing surface even though the adhesive layer is provided.

この水の通9羨けを防水するには、ヒドロゲル含有発泡
体の止水材に、その止水性を最大に発揮させるために、
短時間に発泡体の内部まで水を浸透させることが必要と
なる。
In order to waterproof this water barrier, in order to maximize the water-stopping properties of the hydrogel-containing foam,
It is necessary to allow water to penetrate into the inside of the foam in a short period of time.

本発明はヒドロゲル含有発泡体からなる止水材を短時間
に発泡体の内部まで水を浸透させることができ、止水効
果を向上させた止木材を提供するにある。
The object of the present invention is to provide a water stopper made of a hydrogel-containing foam that allows water to penetrate into the interior of the foam in a short period of time and has an improved water stopper effect.

本発明者は研究の結果、ヒドロゲル含有発泡体中に親水
性の添加剤を分散させると、その表面を伝わって水が内
部に入ヤこむことが分った。この知見に基づいて本発明
を完成した。
As a result of research, the present inventors have found that when a hydrophilic additive is dispersed in a hydrogel-containing foam, water can penetrate into the foam along its surface. The present invention was completed based on this knowledge.

発泡体にヒドロゲルを含ませて止水性を付与するために
は、ヒドロゲルを発泡体に対し、参〜109重量%混在
させることが好ましく、また親水性添加剤の添加量は発
泡体に対し、ダ〜l16重景%で、ヒードロゲルの17
10以上好ましくはi7s以上であ外、また、ヒドロゲ
ルと親水性添加剤の合計添加量は、発泡体に対し、72
0重量%以下であることが好ましい仁とが分った。
In order to impart water-stopping properties to the foam by including the hydrogel, it is preferable to mix the hydrogel in an amount of 109% to 109% by weight with respect to the foam, and the amount of the hydrophilic additive to be added is determined by the amount of the hydrogel relative to the foam. ~l16 % of the hydrogel, 17
10 or more, preferably i7s or more, and the total addition amount of the hydrogel and hydrophilic additive is 72 or more with respect to the foam.
It has been found that the content is preferably 0% by weight or less.

前記の発泡体に対する重量%における発泡体とは、発泡
体中に含有するヒドロゲル、親水性添加剤を除いた発泡
体自身を示す。
The foam in terms of weight % with respect to the foam refers to the foam itself excluding the hydrogel and hydrophilic additives contained in the foam.

親水性添加剤の量がヒドロゲルの量の7770未満にな
ると、水の浸透性を発泡体に付与し得ない。
When the amount of hydrophilic additive is less than 7770 times the amount of hydrogel, it cannot impart water permeability to the foam.

またヒドロゲルと親水性添加剤の合計量が発泡体に対し
120重量%を超えると、発泡体の強度が著しく低下す
るので超えてはならない。
Furthermore, if the total amount of the hydrogel and the hydrophilic additive exceeds 120% by weight based on the foam, the strength of the foam will decrease significantly, so it should not be exceeded.

本発明における発泡体としては、ゴムまたはプラスチッ
クからなるものであればよい。例えばポリアクリル樹脂
、ポリウレタン樹脂、ポリ塩化ビニル−脂、ポリエチレ
ン、ポリプロピレン等のポリオレフィン樹脂、天然ゴム
、エチレン・プロピレンゴム、クロロプレンゴム等の合
成ゴム等の発泡体が挙げられる。なかで本、ポリ塩化ビ
ニル樹彷、エチレン・プロピレンゴム、クロロプレンゴ
ム、ポリウレタン樹脂、特にポリウレタン樹脂の発泡体
が製造の容易性、安定性の点で好ましい。
The foam in the present invention may be made of rubber or plastic. Examples include foamed materials such as polyacrylic resin, polyurethane resin, polyvinyl chloride resin, polyolefin resin such as polyethylene and polypropylene, natural rubber, synthetic rubber such as ethylene/propylene rubber, and chloroprene rubber. Among these, foams of polyvinyl chloride, ethylene/propylene rubber, chloroprene rubber, polyurethane resins, and especially polyurethane resins are preferred in terms of ease of production and stability.

また、発泡体は、0.jK9/c112以上の引張強さ
を有することがシーリング面への貼付は作業を行う上で
好ましい。また、セル数は3.2n当9のセル数がダ〜
tg@であることが好ましく、セル数が参未満では止水
性が低くな19.76個を超えると製造が困−と彦る。
Moreover, the foam is 0. It is preferable to have a tensile strength of jK9/c112 or higher for the purpose of application to a sealing surface. Also, the number of cells is 3.2n per 9 cells.
It is preferable that the cell number is less than 19.76 cells, the water-stopping property is low, and if it exceeds 19.76 cells, production becomes difficult.

ヒドロゲルとしては、例えば澱粉ま九はセルローズにア
クリル系モノマーをグラフト重合させた本のおよびその
アルカリ金属塩、澱粉またはセルローズにアクリルニト
リルをグラフト重合させた後加水分解したもの、ポリア
クリル酸ソーダ架橋物、ポリビニルアルコール無水マレ
イン酸変性物、酢酸ビニル・アクリル酸エステル共重体
けん化物等が挙げられる。しかしこれに限定されるもの
ではなく、自重の数10倍以上の水を吸収する樹脂であ
ればよい。またこれらの粉末粒子径は10メツシユの篩
をパスするものが好ましく、正水性上は細かいものほど
よい。
Hydrogels include, for example, starch maku, which is made by graft polymerizing cellulose with acrylic monomers and its alkali metal salts, starch or cellulose graft polymerized with acrylonitrile and then hydrolyzed, and cross-linked products of sodium polyacrylate. , polyvinyl alcohol modified with maleic anhydride, saponified vinyl acetate/acrylic acid ester copolymer, and the like. However, the material is not limited to this, and any resin that can absorb water several tens of times its own weight or more may be used. Further, the particle size of these powders is preferably one that can pass through a 10-mesh sieve, and the finer the particle size, the better in terms of water quality.

親水性添加剤とは、二価以上のイオンを主成分に含有せ
ず、水との接触角がto0以下、好ましくVip0以下
のものを言う。大別すると有機系と無機系のものとがあ
る。有機系親水性添加剤としては、例えば澱粉、ポリビ
ニルアルコール、カルボキシメチルセルローズ、等が挙
げられる。無機系親水性添加剤としては、ガラス粉、ガ
ラス繊維、ホワイトカーボン、無水けい酸等が挙げられ
る。
A hydrophilic additive is one that does not contain divalent or higher ions as a main component and has a contact angle with water of to0 or less, preferably Vip0 or less. Broadly speaking, there are organic and inorganic types. Examples of organic hydrophilic additives include starch, polyvinyl alcohol, carboxymethyl cellulose, and the like. Examples of the inorganic hydrophilic additive include glass powder, glass fiber, white carbon, and silicic anhydride.

発泡体にヒドロゲルおよび親水性添加剤を加える方法は
、発泡体原料にこれらを混合した後発潜してもよく、あ
るいは発泡体製造後に含浸させてもよい。均一に混合し
たものを得るには前者の方法が好ましい。
The hydrogel and the hydrophilic additive may be added to the foam by mixing them into the foam raw material and then infiltrating them, or by impregnating them after the foam is manufactured. The former method is preferred in order to obtain a uniform mixture.

前記の水との接触角とは、滴形状(松本恒降。The contact angle with water mentioned above refers to the shape of a droplet (Tsunefu Matsumoto).

相好−:高分子化学、 /7 、 !09 (/9JO
> )によって測定した値をいう。
Compatibility: Polymer chemistry, /7, ! 09 (/9JO
> ) refers to the value measured by

実施例1゜ 以下に示す配合比で発泡体を製造した。(部は重量部を
示す。以下同じ) KN−30!OK    三井日曹社ill     
100 部スミカゲル A−u  住友化学社製   
  30  部グラスロン p −32!  旭ファイ
ノく−グラス社製   lS 部F−//l     
 信越化学社製     1 部DABOOJJLV 
  三共エアープOf?、ツ社1%[0,7部水   
                         
 2.2部スタック)  T−9吉富製薬社製    
  。、7部TDI  6!731    日本ポリウ
レタン社製    31.6部得られた発泡体のセル数
は3.2n当′9を個、通気度は0.3 ec/c+w
2. B@c、密度け0.OA!; f /cwt” 
テあった。
Example 1 A foam was manufactured using the following blending ratios. (Parts indicate parts by weight. The same applies hereinafter) KN-30! OK Mitsui Nissosha ill
100 parts Sumikagel A-u manufactured by Sumitomo Chemical Co., Ltd.
Part 30 Glasslon p-32! Asahi Finoku-Glass Co., Ltd. lS part F-//l
Manufactured by Shin-Etsu Chemical Co., Ltd. 1 part DABOOJJLV
Sankyo Airp Of? , Tsusha 1% [0.7 parts water

2.2 parts stack) T-9 manufactured by Yoshitomi Pharmaceutical Co., Ltd.
. , 7 parts TDI 6!731 manufactured by Nippon Polyurethane Co., Ltd. 31.6 parts The number of cells of the obtained foam is 3.2n/'9, and the air permeability is 0.3 ec/c+w
2. B@c, density 0. OA! ;f/cwt”
There was a time.

この発泡体をs cm x s cm X J cs 
(厚す) K 9J り、水槽に浮かべたところ、初期
における重量36コ32であったものが、1時間後に/
J、J 9%2り時間後に31.7 fとなった。
This foam is s cm x s cm X J cs
(Thick) K 9J When I floated it in a water tank, the initial weight was 36 x 32, but after 1 hour it weighed /
J, J It became 31.7 f after 9% 2 hours.

この発泡体を内径B11φ、外径7381φ、厚さ/θ
nに切9、これを1枚は中央に水を通す穴を開けた2枚
のアクリル板で10%圧縮し、アクリル板の中央の穴か
ら0.2’9/C−・minの昇圧速度で水圧をかけ九
ところ、止水圧はλにり/ctn2以上であった。
This foam has an inner diameter of B11φ, an outer diameter of 7381φ, and a thickness of θ
Cut this into n pieces9, compress it by 10% between two acrylic plates, one with a hole in the center for water to pass through, and pressurize at a rate of 0.2'9/C-min from the hole in the center of the acrylic plate. When water pressure was applied at 9, the water stop pressure was more than λ/ctn2.

比較例1゜ 以下に示す配合比で発泡体を製造した。(実施例1に使
用した親水性添加剤のないものンM N −j Oj 
OK     100部スミカゲル A −11730
# F−//ダ      1部 DABOO37LV              O,
7#水                   2.2
#スタツクド ニー9        0J#T D 
I  6373g          J/、t #得
られた発泡体のセル数は3.コ鱈当り7.s q、通気
度は0 、j cc/cm’ 、 66c、密度は0.
06097cmであった。
Comparative Example A foam was manufactured using the following blending ratio: 1°. (The one without the hydrophilic additive used in Example 1)
OK 100 parts Sumikagel A-11730
# F-//da 1 part DABOO37LV O,
7#Water 2.2
#Stacked knee 9 0J#TD
I 6373g J/, t #The number of cells of the obtained foam is 3. 7. per cod. s q, air permeability is 0, j cc/cm', 66c, density is 0.
It was 06097 cm.

この発泡体を実施例1と同様な大きさに切り、水槽試験
を行ったところ、初期の重量3.Ofが7時間後は1.
21f、1時間後け/9.! ?であった。
When this foam was cut into the same size as in Example 1 and subjected to a water tank test, the initial weight was 3. After 7 hours, 1.
21f, 1 hour later/9. ! ? Met.

また実施例1と同様にして止を圧を試験したところ、止
水圧は0.71C97cm2であったっ実施例2 以下に示す配合比で発泡体を製造した。
In addition, when the water stop pressure was tested in the same manner as in Example 1, the water stop pressure was 0.71C97 cm2. Example 2 A foam was manufactured using the blending ratio shown below.

KN−3030に100部 スミカゲル A−俊                
30#p−//ダ                 
   /、Q tDABCOJJ LV       
      O,7部水              
                    2.21ス
タックド丁−?                  
Q、3yT D I  ts/is         
        3.。
100 parts Sumikagel A-Shun in KN-3030
30#p-//da
/,Q tDABCOJJ LV
O, 7 parts water
2.21 Stacked Ding-?
Q, 3yT D I ts/is
3. .

得られた発泡体のセル数は3.コn当り7k個、jM 
気度1lt0.3 cc/c*2− sec 、密度は
0.0t3 f/CI++’ テあった。
The number of cells of the obtained foam was 3. 7k pieces per con, jM
The air temperature was 1lt0.3cc/c*2-sec, and the density was 0.0t3f/CI++'te.

発泡体を実施例1におけると同様にして水槽試験および
止水試験を行った。
The foam was subjected to a water tank test and a water stop test in the same manner as in Example 1.

初期の重量はJ、1k Fであったが、1時間後は/コ
、7f、20時間後はJJ、、2 tとなった。止水圧
はコKy/c−以上であつ九。
The initial weight was J, 1kF, but after 1 hour it was /K, 7f, and after 20 hours it was JJ, 2t. The water stop pressure is ky/c- or more.

以上のように本発明の止水材は優れた止水性を持つもの
である。
As described above, the water-stopping material of the present invention has excellent water-stopping properties.

特許出願人 日本発条株式会社Patent applicant: NHK Spring Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 発泡体に対し、水不溶性の吸水性樹脂粉末(以下ヒドロ
ゲルと言う)を参〜109重量%、親水性添加剤をダ〜
iit重量%、かつ親水性添加剤の添jXlllヒドロ
ゲル量のl/10以上で、ヒドロゲルと親水性添加剤の
合計添加量が発泡体に対しlコO重量重量下であるよう
に発泡体に混在させたことを特徴とする発泡体止水材。
The foam contains ~109% by weight of water-insoluble water-absorbing resin powder (hereinafter referred to as hydrogel) and ~109% by weight of a hydrophilic additive.
iit% by weight, and the amount of hydrophilic additive added is 1/10 or more of the amount of hydrogel, and the total amount of hydrogel and hydrophilic additive is mixed in the foam such that the total amount of added hydrogel and hydrophilic additive is less than 1% by weight of the foam. A foam water stop material characterized by:
JP20526481A 1981-12-21 1981-12-21 Water-stopping material Pending JPS58108232A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20526481A JPS58108232A (en) 1981-12-21 1981-12-21 Water-stopping material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20526481A JPS58108232A (en) 1981-12-21 1981-12-21 Water-stopping material

Publications (1)

Publication Number Publication Date
JPS58108232A true JPS58108232A (en) 1983-06-28

Family

ID=16504097

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20526481A Pending JPS58108232A (en) 1981-12-21 1981-12-21 Water-stopping material

Country Status (1)

Country Link
JP (1) JPS58108232A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62246941A (en) * 1986-04-19 1987-10-28 Daiichi Kagaku:Kk Preparation of crosslinked foam of polyethylene resin having water-absorbing property and retentivity of absorbed water
JPH08157805A (en) * 1994-12-05 1996-06-18 Nhk Spring Co Ltd Water-swelling sealing material having crosslinked and foamed structure
WO1998000181A1 (en) * 1996-07-01 1998-01-08 Woodbridge Foam Corporation Foamed polymer and process for production thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53108165A (en) * 1977-03-03 1978-09-20 Toho Rayon Co Ltd Hygroscopic foam and its preparation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53108165A (en) * 1977-03-03 1978-09-20 Toho Rayon Co Ltd Hygroscopic foam and its preparation

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62246941A (en) * 1986-04-19 1987-10-28 Daiichi Kagaku:Kk Preparation of crosslinked foam of polyethylene resin having water-absorbing property and retentivity of absorbed water
JPH08157805A (en) * 1994-12-05 1996-06-18 Nhk Spring Co Ltd Water-swelling sealing material having crosslinked and foamed structure
WO1998000181A1 (en) * 1996-07-01 1998-01-08 Woodbridge Foam Corporation Foamed polymer and process for production thereof

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