JPS63214573A - Seal material - Google Patents

Seal material

Info

Publication number
JPS63214573A
JPS63214573A JP4628087A JP4628087A JPS63214573A JP S63214573 A JPS63214573 A JP S63214573A JP 4628087 A JP4628087 A JP 4628087A JP 4628087 A JP4628087 A JP 4628087A JP S63214573 A JPS63214573 A JP S63214573A
Authority
JP
Japan
Prior art keywords
parts
foam
coated
foaming layer
seal member
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
JP4628087A
Other languages
Japanese (ja)
Other versions
JP2634591B2 (en
Inventor
Nozomi Ohashi
大橋 望
Sadayuki Inagaki
稲垣 定行
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.)
Nitto Denko Corp
Original Assignee
Nitto Electric Industrial 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 Nitto Electric Industrial Co Ltd filed Critical Nitto Electric Industrial Co Ltd
Priority to JP62046280A priority Critical patent/JP2634591B2/en
Publication of JPS63214573A publication Critical patent/JPS63214573A/en
Application granted granted Critical
Publication of JP2634591B2 publication Critical patent/JP2634591B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To maintain good waterproofness for a long time by providing a coated foaming layer on at least one face of a porous seal member which has a rough surface and exerts the waterproofness when compressed. CONSTITUTION:A coated foaming layer with the same or preferably more flexibility than a porous seal member and a practically smooth surface is provided on the surface (the face to be brought into contact with the stuck body face at the application position) of this porous seal member such as a polyurethane foaming body and felt. Thereby, the porous seal member and the coated foaming layer are integrated at the interface, both of them are firmly stuck, and the adhesion between the stuck body face and the coated foaming layer constituting a seal material at the application position is excellent. In addition, the coated foaming layer absorbs the bending distortion and generates no wrinkle, thus good waterproofness is maintained for a long time.

Description

【発明の詳細な説明】 〈産業上′の利用分野〉 本発明はシール材料に関するもので、更に詳しくは特に
シール材料を湾曲或いは屈曲させて使用した場合に良好
な防水特性を発揮するシール材料を提供するものである
[Detailed Description of the Invention] <Industrial Field of Application> The present invention relates to a sealing material, and more particularly to a sealing material that exhibits good waterproof properties when used in a curved or bent manner. This is what we provide.

〈従来技術及びその問題点〉 従来、ポリウレタン発泡体にアスファルトやコールター
ルを含浸してなるタイプや、エチレン−プロピレン−タ
ーポリマーゴムに撓水性及び粘着性にすぐれる樹脂を添
加してなる混和物をシート状に成形して発泡加硫してな
るタイプなどの多孔質系のシール材料は知られている。
<Prior art and its problems> Conventionally, there have been types made of polyurethane foam impregnated with asphalt or coal tar, and mixtures made of ethylene-propylene-terpolymer rubber with the addition of resins with excellent water repellency and adhesiveness. Porous sealing materials, such as those made by molding into a sheet and foaming and vulcanizing, are known.

かかる多孔質系シール材料は、施工場所がほぼ直線上で
あれば1例えば30〜95%まで圧縮することにより目
的とする防水特性が得られるものであるが、施工場所が
湾曲或いは屈曲している場合は、シール材料の折り曲げ
によって、シール材料の表面に微細なシワが入り、これ
が水ミチの役割を果すために漏水するという欠点があっ
た。
Such porous sealing materials can obtain the desired waterproof properties by compressing them to, for example, 30 to 95% if the construction site is on a substantially straight line, but if the construction site is curved or bent. In this case, the bending of the sealing material creates minute wrinkles on the surface of the sealing material, which act as water grooves and cause water to leak.

かかるシール材料のシワを防止するために、シール材料
の表面にプラスチックフィルムを接着剤。
Glue the plastic film on the surface of the sealing material to prevent wrinkles of the sealing material.

融着、溶着などの接着手段を用いて貼着する試みもなさ
れているが1両者の強固な接着が得られないこと、フィ
ルムの貼着によって発泡体の柔軟性が減少して目的とす
る追従性が得られないこと。
Attempts have been made to attach using adhesive means such as fusion and welding, but 1. Strong adhesion between the two parts cannot be obtained, and the flexibility of the foam decreases due to the attachment of the film, making it difficult to achieve the desired tracking. Not being able to have sex.

などの不都合を有するものである。It has the following disadvantages.

く問題点を解決するための手段〉 本発明はかかる従来技術の欠点を解決した新規なシール
材料を提供するものであって、その要旨とするところは
、圧縮することによって防水性を発揮する、表面が粗面
である多孔性シール部材の少なくとも一方の面に、塗設
発泡層を設けてなることにある。
Means for Solving the Problems> The present invention provides a new sealing material that solves the drawbacks of the prior art, and its gist is that it exhibits waterproof properties by being compressed. A coating foam layer is provided on at least one surface of a porous sealing member having a rough surface.

本発明によれば、多孔性シール部材と塗設発泡層との接
着が強固で、しかも施工場所の被着体面吸収してシワを
起生ずることがないので、長期に亘って良好な防水性を
維持するという特徴を有する。
According to the present invention, the adhesion between the porous sealing member and the applied foam layer is strong, and it does not absorb the surface of the adherend at the installation site and cause wrinkles, so good waterproof properties can be maintained for a long time. It has the characteristic of maintaining.

本発明の実施に当って用いられる多孔性シール部材は、
通常30〜95%まで圧縮することによシ防水性を発揮
するが1表面は発泡体のスライス面又はシート状繊維体
面の如き表面が粗面であるものである。前記部材には一
方の表面がスライス面で他方の表面が緻密なスキン様面
である発泡体も含まれる。
The porous sealing member used in carrying out the present invention is
Normally, waterproof properties are exhibited by compressing the material to 30 to 95%, but one surface is rough, such as the sliced surface of a foam or the surface of a sheet-like fibrous material. The member may also include a foam having a sliced surface on one surface and a dense skin-like surface on the other surface.

このような多孔性シート部材としては、ポリウレタン発
泡体、フェルト、厚手不織布単体或いはこれら多孔性材
料にアスファルト、コールタール。
Such porous sheet members include polyurethane foam, felt, thick nonwoven fabric alone, or these porous materials with asphalt or coal tar.

合成ゴム、合成樹脂の如き防水性組成物を含浸保持させ
たもののほか、或いはエチレン−プロピレン−ターポリ
マーゴム、ブチルゴムに代表されるゴム類などに、椀水
性及び粘着性を有する軟化物質及び/又は樹脂類を添加
してなる混和物をシート状等に成形して発泡加硫後所定
の厚み或いは幅にスライス(切断)することによって得
られたものが挙げられる。
In addition to impregnated and retained waterproof compositions such as synthetic rubbers and synthetic resins, or rubbers such as ethylene-propylene-terpolymer rubber and butyl rubber, softening substances and/or adhesives that have water resistance and adhesive properties can be used. Examples include those obtained by molding a mixture with resins into a sheet shape, foaming and vulcanizing it, and then slicing (cutting) it into a predetermined thickness or width.

このように構成された多孔性シート部材の表面(施工場
所の被着体面に当接される面)には、該部材と同等、好
ましくはそれ以上の柔軟性を有し。
The surface of the porous sheet member configured in this way (the surface that comes into contact with the surface of the adherend at the construction site) has flexibility equal to, and preferably greater than, that of the member.

しかも表面が実質的に平滑な塗設発泡層が設けられ1本
発明のシール材料とされる。
Moreover, a coated foam layer with a substantially smooth surface is provided, making it a sealing material of the present invention.

このような表面が実質的に平滑な塗設発泡j−は、以下
の((イ)〜((ホ)示すような方法によって形成され
た塗設発泡層が柔軟性と平滑性及び撓水性にすぐれるの
で好ましいものである。
Such coated foam j- with a substantially smooth surface has a coated foam layer formed by the following methods ((a) to (e)) that has flexibility, smoothness, and water repellency. It is preferable because it is excellent.

(イ)コムラテックスを主成分とし、これに起泡剤。(a) Com latex as the main ingredient, plus a foaming agent.

構造強化剤、さらに必要に応じて接着性付与樹脂とを配
合してなる配合物を機械撹拌して、3〜500ポイズ、
好ましくは10〜300ボイズ(各れもat25“C)
の粘度に調整してなる微細泡含有水分散高分子材料を多
孔性シール部材上に、厚みが1〜3000μ惟、好まし
くは50〜1000μ惰の範囲となるように直接塗布し
、通常70〜90℃で1〜3分間予備乾燥して後、10
0〜200℃で2〜15分間乾燥することによって塗布
厚と略々同一厚みの発泡層が得られる。
A composition containing a structural reinforcing agent and, if necessary, an adhesion-imparting resin is mechanically stirred to give a pressure of 3 to 500 poise,
Preferably 10 to 300 voices (each at25"C)
A microfoam-containing water-dispersed polymeric material adjusted to a viscosity of After pre-drying for 1-3 minutes at ℃,
By drying at 0 to 200°C for 2 to 15 minutes, a foamed layer having approximately the same thickness as the coating thickness can be obtained.

前記配合物は、天然ゴム(NR)、カルボキシル基変性
スチレン−ブタジェンゴム(C−8BR)。
The blends are natural rubber (NR) and carboxyl group-modified styrene-butadiene rubber (C-8BR).

ニトリルブタジェンゴム(NBR)、7クリルゴムなど
のゴム類或いはポリ塩化ビニル、ポリ塩化ビニリデン、
ポリエチレンなどの合成樹脂類からなるラテックス(固
形分は40〜70重量%が好ましく)の固形分100重
量部に対して、ステアリン酸アンモニウム塩、オレイン
酸カリ、アルキルスルホサクシナメートの如き起泡剤を
3〜8重量部、メトオキシメチロールメラミン、イオウ
、エポキシ樹脂の如き薄層のマトリックス強度を向とさ
せる構造強化剤を2〜10重量部、テルペン系[JIl
l、テルペンフェノール系m脂、ロジン、ロジン誘導体
、石油系樹脂の如き接着性付与樹脂を0〜200重量部
、好ましくは10〜100重量部夫々配合してなるもの
であることが望ましいものである。しかして、この配合
物には更に増粘剤、充填剤、構造強化助剤、pH調整剤
などを添加することができる。
Rubbers such as nitrile butadiene rubber (NBR), 7cryl rubber, polyvinyl chloride, polyvinylidene chloride,
Foaming agents such as ammonium stearate, potassium oleate, and alkyl sulfosuccinamate are added to 100 parts by weight of latex (preferably solids content is 40 to 70% by weight) made of synthetic resins such as polyethylene. 3 to 8 parts by weight of methoxymethylolmelamine, sulfur, 2 to 10 parts by weight of a structural reinforcing agent that improves the matrix strength of the thin layer such as methoxymethylolmelamine, sulfur, and epoxy resin, and terpene-based [JIl
It is desirable that the composition contains 0 to 200 parts by weight, preferably 10 to 100 parts by weight of adhesion-imparting resins such as l, terpene phenol type fat, rosin, rosin derivatives, and petroleum resins. . Thus, further thickeners, fillers, structural reinforcement aids, pH regulators, etc. can be added to the formulation.

このように構成してなる配合物は、1(10〜3000
回転/分する機械撹拌機で通常1〜10分間混合撹拌さ
れて、系中に1〜1000μ惰の微細な起泡を含む、3
〜SOOボイズ(at25℃)の水分散高分子材料とさ
れる。該材料の粘度が3ポイズ(at25℃)未満では
、起泡を含有するとは言え、多孔性シール部材中に含浸
されることがあるために好ましくなく、SOOデイズ(
at25℃)を超えると塗工しずらくなるので好ましく
ないものである。
The composition constituted in this way has a concentration of 1 (10 to 3000
Mixed and stirred for usually 1 to 10 minutes with a mechanical stirrer that rotates per minute, containing fine foam of 1 to 1000μ in the system.
It is considered to be a water-dispersed polymer material with ~SOO voids (at 25°C). If the viscosity of the material is less than 3 poise (at 25°C), although it contains foam, it is not preferable because it may be impregnated into the porous sealing member, and SOO days (
If the temperature exceeds (at 25°C), coating becomes difficult, which is not preferable.

このように調整された水分散高分子材料は、前述の如く
、シール部材の片面又は両面に所定の厚みとなるように
直接塗布され、その後乾燥することより水分散高分子材
料中の微細泡が大きさ及び形に実質的な変更なく、1〜
1000μ溝 の微細な泡を含む1〜20倍、好ましく
は2〜13倍発泡の表面が平滑な塗設発泡層とされる。
As mentioned above, the water-dispersed polymer material prepared in this way is directly applied to one or both sides of the sealing member to a predetermined thickness, and then dried to eliminate the microbubbles in the water-dispersed polymer material. 1 to 1 without substantial change in size and shape
The coated foam layer is foamed 1 to 20 times, preferably 2 to 13 times, and has a smooth surface, containing fine bubbles of 1000 micron grooves.

(ロ)(イ)の方法において用いられる配合物にさらに
ワックス、パラフィン、シリコーンオイルの如き接水性
物質を0.1〜70重量%の範囲で添加してなるものを
用いて表面が平滑な塗設発泡層とされる。
(b) A coating with a smooth surface is obtained by adding a water-wetting substance such as wax, paraffin, or silicone oil in a range of 0.1 to 70% by weight to the formulation used in method (a). It is considered to be a foam layer.

この方法にて形成した塗設発泡によれば1層目体にさら
に接水性が付与さiするので防水性がより向とする。
The coating foam formed by this method further imparts water contact properties to the first layer body, thereby improving waterproofness.

(ハ) アクリル系樹脂、ポリ塩化ビニル樹脂、ポリオ
レフィン系樹脂、天然ゴム、エチレンプロピレンターポ
リマー、スチレンブタジェンゴムなどの高分子材料10
0重量部に対して、ジオクチルフタレート、石油系オイ
ル、プロセスオイル、パラフィン、潤滑油、コールター
ル、脂肪族系油、ロウ、低分子量ゴム、アタックチック
ポリプロピレンの如き軟化剤0〜200重量部、ジニト
ロソペンタメチレンテトラミン、アゾジカルボンアミド
(c) Polymer materials 10 such as acrylic resin, polyvinyl chloride resin, polyolefin resin, natural rubber, ethylene propylene terpolymer, styrene butadiene rubber, etc.
0 to 200 parts by weight of a softening agent such as dioctyl phthalate, petroleum oil, process oil, paraffin, lubricating oil, coal tar, aliphatic oil, wax, low molecular weight rubber, attack polypropylene, Nitrosopentamethylenetetramine, azodicarbonamide.

バラトルエンスルフォニルヒドラジン、tj[ナトリウ
ムの如き発泡剤1〜20重量部、硫黄、メチロールメラ
ミン、エポキシ樹脂、キノンジオキシム、パーオキサイ
ドの如き構造強化剤0.5〜10重を部とを含むもので
あり、その他必要に応じて充填剤、顔料、滑剤、紫外線
吸収剤などを配合することができる。
containing 1 to 20 parts by weight of a blowing agent such as balatoluenesulfonylhydrazine, tj[sodium, and 0.5 to 10 parts by weight of a structural reinforcement such as sulfur, methylol melamine, epoxy resin, quinone dioxime, peroxide. Other fillers, pigments, lubricants, ultraviolet absorbers, etc. can be added as necessary.

該高分子材料は、有機溶剤に溶解するか、水に分散せし
めて、3〜500ポイズ(at25°C)の粘度に調整
するか、或いは発泡剤の分解温度以下の温度で溶融し、
多孔性シール部材とに、厚みが1〜3000μ溝、好ま
しくは100〜1000μ溝となるように直接塗布し1
通常60〜200℃で1〜20分間、必要に応じてロー
ル等の圧縮下で加熱することによって発泡加硫し、平滑
な表面を有する塗設発泡層を形成する。
The polymeric material is dissolved in an organic solvent or dispersed in water and adjusted to a viscosity of 3 to 500 poise (at 25°C), or melted at a temperature below the decomposition temperature of the blowing agent,
Directly apply it to the porous sealing member so that the thickness is 1 to 3000μ grooves, preferably 100 to 1000μ grooves.
Foaming and vulcanization is usually carried out by heating at 60 to 200° C. for 1 to 20 minutes, if necessary under compression using a roll, etc., to form a coated foam layer having a smooth surface.

に)(ハ)で用いた高分子材料をトルエン、ヘキサン、
アセトン、酢酸エチルなどの溶液又はジオクチルフタレ
ート、ジブチルフタレートなどの可塑剤などを用いて溶
解し、これにシリコーンオイルの如き界面張力低減剤を
、1〜10重量%となるように添加し、必要に応じて架
橋剤、充填剤、顔料などの配合剤を添加して機械撹拌し
て微細泡含有溶液高分子材料を作成し、以下前記(イ)
と同様の操作にて塗設発泡/11を形成する。
(b) The polymer materials used in (c) are mixed with toluene, hexane,
Dissolve using a solution such as acetone or ethyl acetate or a plasticizer such as dioctyl phthalate or dibutyl phthalate, and add an interfacial tension reducing agent such as silicone oil to a concentration of 1 to 10% by weight, as necessary. Add compounding agents such as crosslinking agents, fillers, and pigments according to the requirements and mechanically stir to create a solution polymeric material containing microbubbles, as described in (a) below.
Coating foam/11 is formed in the same manner as above.

((ホ)(イ)のラテックス又は(ハ)の高分子材料溶
液に、これにマイクロカプセル又はアクリロニトリルか
らなる膨張した中空微小球を分散し、必要に応じて架橋
剤、充填剤などの配合剤を添加し、とfLを乾燥後の厚
みが1〜3000μ常となるように塗布乾燥して塗設発
泡Imを形成する。
((e) Disperse microcapsules or expanded hollow microspheres made of acrylonitrile in the latex of (a) or the polymeric material solution of (c), and add compounding agents such as crosslinking agents and fillers as necessary. and fL are coated and dried so that the thickness after drying is usually 1 to 3000 μm to form a coated foam Im.

このような塗設発泡層は多孔性シール部材の両面がスラ
イス面の如き粗面である場合には、両表面に形成し、さ
らにその一方の面にゴム及び/又は合成樹脂類を主体と
する常温で感圧接着性を示す物質からなる粘着層を約0
.1〜1.5罪の厚みで形成してもよいが、例えば塗設
発泡層を一方の表面に構成し、他方の表面に粘着層を構
成してもよいものである。
When both surfaces of the porous sealing member are rough surfaces such as sliced surfaces, such a coating foam layer is formed on both surfaces, and one surface is coated with rubber and/or synthetic resin as the main material. The adhesive layer made of a material that exhibits pressure-sensitive adhesive properties at room temperature is approximately 0.
.. Although it may be formed to a thickness of 1 to 1.5 mm, for example, a coated foam layer may be formed on one surface and an adhesive layer may be formed on the other surface.

〈効果〉 本発明のシール材料は以上の如く、多孔性シール部材の
表面に1発泡材料を直接塗布して発泡層を形成したので
部材面と発泡層との界面は一体化しており、従って両者
の接着は強固であり、しかもシール材料を湾曲或いは屈
曲させても発泡層が変形による歪を吸収するので水ミチ
が形成されることがなく長期に亘って良好な防水性が得
られるという特徴を有する。
<Effects> As described above, in the sealing material of the present invention, since a foamed material is directly applied to the surface of a porous sealing member to form a foamed layer, the interface between the member surface and the foamed layer is integrated, and therefore both The adhesion is strong, and even if the sealing material is bent or bent, the foam layer absorbs the distortion caused by deformation, so no water grooves are formed and good waterproof properties can be obtained over a long period of time. have

〈実施例〉 以下1本発明の実施例を示す。文中1部或いは%とある
のはそれぞれ重量部或いは重量%を意味する。
<Example> Below, one example of the present invention will be shown. In the text, 1 part or % means part by weight or % by weight, respectively.

実施例1 アクリルゴムラテックス(固型分60%)100部エポ
キシ系樹脂水分散液(固型分80%)10部オレイン酸
カリ石鹸(固型分35%)    5部アルキン酸ソー
ダ水溶液(固型分2%)   1部アンモニア水(固型
分35%)       3部上記配合物を機械撹拌機
で混合撹拌して略3倍に起泡させ、これを発泡倍率約3
0倍の厚さ101mのエーテル系ポリウレタンフォーム
のスライス面に約100μ鴨の厚みとなるようにドクタ
ーナイフを用いて直接塗布し、約80℃で1分間予備加
熱を行い1次いで約140℃で1部分間加熱して塗布層
を架橋し、スライス面に約100μ惰厚の塗設発泡層を
有するシ→ル材を得た。
Example 1 Acrylic rubber latex (solid content 60%) 100 parts Epoxy resin aqueous dispersion (solid content 80%) 10 parts Potassium oleate soap (solid content 35%) 5 parts Sodium alkinate aqueous solution (solid content) 2%) 1 part ammonia water (solid content 35%) 3 parts The above mixture was mixed and stirred with a mechanical stirrer to foam approximately 3 times the volume, and this was foamed to a foaming ratio of approximately 3.
It was applied directly to the sliced surface of 101 m thick ether-based polyurethane foam using a doctor knife to a thickness of about 100 μm, preheated at about 80°C for 1 minute, and then heated at about 140°C for 1 minute. The coated layer was crosslinked by heating between sections to obtain a seal material having a coated foam layer on the sliced surface with a thickness of about 100 μm.

実施例2 カルボキシル基変性スチレン−ブタジェンゴムラテック
ス(固型分60%)       100部メラミン系
樹脂水分散液(固型分80%) 5部ステアリン酸アン
モニウム塩水分散液(固型分35%)        
             2部カルボキシメチルセル
ロース水溶液(固型分2%)2部 アンモニア水(固型分35%)       2部クレ
ー                 50部ワックス
水分散液(固型分50%)10部と記配合物を機械撹拌
機で混合撹拌して略5倍に起泡させ、これをエチレン−
プロピレンターポリマーと炭酸カル:、/:x’)f)
J−との混和物を硫黄加硫して7倍に発泡させた厚さ3
 raw、のゴムフオームのスライス面に約2000μ
溝の厚みとなるようにドクターナイフを用いて直接塗布
し、以下実施例1と同様の操作で、スライス面に約20
00μ悔厚の塗設発泡INを有するシール材を得た。
Example 2 Carboxyl group-modified styrene-butadiene rubber latex (solid content 60%) 100 parts melamine resin aqueous dispersion (solid content 80%) 5 parts ammonium stearate salt aqueous dispersion (solid content 35%)
2 parts carboxymethylcellulose aqueous solution (solid content 2%) 2 parts ammonia water (solid content 35%) 2 parts clay 50 parts Wax aqueous dispersion (solid content 50%) 10 parts and the above mixture were mixed with a mechanical stirrer. Mix and stir to foam approximately 5 times, and add ethylene-
Propylene terpolymer and Cal carbonate:, /:x')f)
Thickness 3 made by sulfur vulcanization of the mixture with J- and foaming to seven times the size.
Approximately 2000μ on the sliced surface of raw rubber foam
Apply directly using a doctor knife so that it has the thickness of the groove, and then apply it to the sliced surface in the same manner as in Example 1.
A sealing material having a coating foamed IN having a thickness of 00 μm was obtained.

実施例3 天然ゴム100部、硫黄3部、酸化亜鉛3部、ジチオカ
ルバメート1部、ジニトロソペンタメチレンテトラミン
5部、ステアリン酸2部1石油系オイル20部及び尿素
5部の配合物をゴム用バンバリーミキサ−にて混練した
後、トルエンを添加して粘度10000CPS (at
 20℃)、固型分50%の溶液を得る。
Example 3 A blend of 100 parts of natural rubber, 3 parts of sulfur, 3 parts of zinc oxide, 1 part of dithiocarbamate, 5 parts of dinitrosopentamethylenetetramine, 2 parts of stearic acid, 20 parts of petroleum oil, and 5 parts of urea was prepared for rubber. After kneading in a Banbury mixer, toluene was added to give a viscosity of 10,000 CPS (at
20° C.) to obtain a solution with a solids content of 50%.

該溶液を実施例2のゴムフオームのスライス面に100
0μ愼の厚みで直接塗布し、170℃で10分加熱して
塗布層を加熱発泡し、スライス面に約1200μ惧の塗
設発泡層を有するシール材を得た。
The solution was applied to the sliced surface of the rubber foam of Example 2 at a rate of 100%.
The sealant was directly applied to a thickness of 0 μm and heated at 170° C. for 10 minutes to heat and foam the applied layer to obtain a sealing material having a foamed layer of about 1200 μm thick on the sliced surface.

実施例4 ポリ塩化ビニル100部、ジオクチルフタレート80部
、二塩性亜リン酸鉛2部及びシリコーンオイル3部から
なる配合物を機械撹拌機にて混合撹拌して略3倍に起泡
させ、これを実施例の?リウレタンフオームのスライス
面に500μ溝の厚ミとなるようにドクターナイフを用
いて直接塗布し、190℃で10分加熱して、スライス
Ill約500μ慣の塗設発泡J−を有するシール材を
得た。
Example 4 A mixture consisting of 100 parts of polyvinyl chloride, 80 parts of dioctyl phthalate, 2 parts of dichloride lead phosphite, and 3 parts of silicone oil was mixed and stirred using a mechanical stirrer to foam approximately three times as much. Is this an example? It was applied directly to the sliced surface of the urethane foam using a doctor knife so as to have a groove thickness of 500μ, and heated at 190°C for 10 minutes to obtain a sealing material having a coating foam J- of about 500μ per slice. Ta.

実施例5 アクリルゴムラテックス(固型分60%)100部 ポリビニルアルコール水溶液(固型分5%)2部 メラミン系樹脂水分散液(固型分80%)2部アンモニ
ア水(固型分35%)      2部アワリロニトリ
ルからなる膨張させた中空微小球(粒径60〜150μ
惰)        3部上記配合物からなる粘度15
000CPS(at 20℃)の溶液を実施例2のゴム
フオームのスライス面に200μ惰の厚みとなるように
ドクターナイフを用いて直接塗布し、120℃で10分
間加熱して。
Example 5 Acrylic rubber latex (solid content 60%) 100 parts Polyvinyl alcohol aqueous solution (solid content 5%) 2 parts Melamine resin aqueous dispersion (solid content 80%) 2 parts Aqueous ammonia (solid content 35%) ) Expanded hollow microspheres consisting of two parts avalylonitrile (particle size 60-150μ
Viscosity 15 consisting of 3 parts of the above formulation
A solution of 000 CPS (at 20° C.) was applied directly to the sliced surface of the rubber foam of Example 2 to a thickness of 200 μm using a doctor knife, and heated at 120° C. for 10 minutes.

比重0,5の塗設発泡層をスライス面に有するシール材
を得た。
A sealing material having a coated foam layer with a specific gravity of 0.5 on the sliced surface was obtained.

第1表に実施例1〜5の特性評価結果を示す。Table 1 shows the characteristics evaluation results of Examples 1 to 5.

第1表中の比較例1は実施例1のポリウレタンフt−A
を、比較例2は実施例2のゴムフオームをシール材料と
して夫々用いたものである。
Comparative Example 1 in Table 1 is the polyurethane foam t-A of Example 1.
In Comparative Example 2, the rubber foam of Example 2 was used as a sealing material.

第1表中の測定法は、第1図及び第2図に示す如く、実
施例1〜5及び比較例1〜2で得た幅1゜關のシール材
料1の非塗設発泡層面(比較例1〜2は片面のみ)に・
厚さ0.3mのブチルゴム系粘着層2を常法により設け
てこれをガラス板3の表面に100 m Hの湾曲を付
けて貼着し、その上にガラス板3′を重ね合せ、図示省
略しである治具を用いて実施例1.4及び比較例1は8
0%まで圧縮し、実施例2,3.・5及び比較例2は5
0%まで圧縮して測定具を作成し、シール材料で構成し
た空洞に水を水深が100fiとなるように注入し。
The measurement method in Table 1 is as shown in FIG. 1 and FIG. Examples 1 and 2 are on one side only)
A butyl rubber-based adhesive layer 2 with a thickness of 0.3 m is provided by a conventional method and adhered to the surface of a glass plate 3 with a curvature of 100 m H, and a glass plate 3' is superimposed on it, not shown. Example 1.4 and Comparative Example 1 were prepared using the same jig.
Compressed to 0%, Examples 2, 3.・5 and comparative example 2 are 5
A measurement tool was created by compressing it to 0%, and water was injected into the cavity made of sealing material to a depth of 100fi.

シール材料とガラス板3との界面からの捕水の有無を所
定時間ごとに観察した。
The presence or absence of water capture from the interface between the sealing material and the glass plate 3 was observed at predetermined intervals.

第  1  表 第1表中の判定は、漏水が全く認められないものを○と
し、僅かに漏水が認められるものを△とし、明らかに漏
水が認められるものを×とした。
Table 1 The evaluation in Table 1 is as follows: ○ indicates that no water leakage is observed, △ indicates that slight water leakage is observed, and × indicates that water leakage is clearly observed.

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

第1図は本発明のシール材料の特性を評価するための測
定具の正面図、第2図は第1図をI −I’線で切断し
た断面図である。 1・・・シール材料  4・・・塗設発泡層第1図 第2wJ 2−−御粘1溝 3.3’−一一汐゛°ンス板 4−−”!設置 手続補正書 昭和62年 6 月 8 日 1、事件の表示 昭和62年特許願第 46280   号2、発明の名
称 シール材料 3、補正をする者 事件との関係  特許出願人 郵便番号    567 4、手続補正指令の日付 昭和62年5月26日5、補
正の対象 発明の名称が「シール材」とあるのを「シール材料」と
補正します。 以上
FIG. 1 is a front view of a measuring tool for evaluating the characteristics of the sealing material of the present invention, and FIG. 2 is a cross-sectional view of FIG. 1 taken along line I-I'. 1... Seal material 4... Coated foam layer Figure 1 2wJ 2--Glue 1 groove 3.3'-11 tidal spring plate 4--"! Installation procedure amendment 1986 June 8th 1, Indication of the case Patent Application No. 46280 of 1988 2, Name of the invention Seal material 3, Person making the amendment Relationship to the case Patent applicant postal code 567 4, Date of procedural amendment order 1988 On May 26, 5, the name of the invention subject to amendment is amended from "Sealing material" to "Sealing material."that's all

Claims (1)

【特許請求の範囲】 1)圧縮することによって防水性を発現する、表面が粗
面である多孔性シール部材の少なくとも一方の面に、塗
設発泡層を設けてなるシール材料。 2)一方の表面に粘着層を設けてなる特許請求の範囲第
1項記載のシール材料。
[Scope of Claims] 1) A sealing material comprising a coated foam layer provided on at least one surface of a porous sealing member with a rough surface that exhibits waterproof properties when compressed. 2) The sealing material according to claim 1, wherein an adhesive layer is provided on one surface.
JP62046280A 1987-02-27 1987-02-27 Seal material Expired - Lifetime JP2634591B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62046280A JP2634591B2 (en) 1987-02-27 1987-02-27 Seal material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62046280A JP2634591B2 (en) 1987-02-27 1987-02-27 Seal material

Publications (2)

Publication Number Publication Date
JPS63214573A true JPS63214573A (en) 1988-09-07
JP2634591B2 JP2634591B2 (en) 1997-07-30

Family

ID=12742819

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62046280A Expired - Lifetime JP2634591B2 (en) 1987-02-27 1987-02-27 Seal material

Country Status (1)

Country Link
JP (1) JP2634591B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017199950A1 (en) * 2016-05-17 2017-11-23 三井化学株式会社 Seal member, manufacturing method therefor, vehicle door, and building door

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51141755U (en) * 1975-05-07 1976-11-15
JPS54159552A (en) * 1978-06-06 1979-12-17 Toyo Cloth Co Gasket and its manufacturing method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51141755U (en) * 1975-05-07 1976-11-15
JPS54159552A (en) * 1978-06-06 1979-12-17 Toyo Cloth Co Gasket and its manufacturing method

Also Published As

Publication number Publication date
JP2634591B2 (en) 1997-07-30

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