JPS61174282A - Adhesive for anticorrosive tape - Google Patents

Adhesive for anticorrosive tape

Info

Publication number
JPS61174282A
JPS61174282A JP1357785A JP1357785A JPS61174282A JP S61174282 A JPS61174282 A JP S61174282A JP 1357785 A JP1357785 A JP 1357785A JP 1357785 A JP1357785 A JP 1357785A JP S61174282 A JPS61174282 A JP S61174282A
Authority
JP
Japan
Prior art keywords
adhesive
hydroxyl group
tape
diene polymer
anticorrosive
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
JP1357785A
Other languages
Japanese (ja)
Other versions
JPH0361713B2 (en
Inventor
Yuzo Kurashige
倉重 友三
Matsunori Yasuyoshi
松則 安吉
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.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical 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 Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP1357785A priority Critical patent/JPS61174282A/en
Publication of JPS61174282A publication Critical patent/JPS61174282A/en
Publication of JPH0361713B2 publication Critical patent/JPH0361713B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Adhesives Or Adhesive Processes (AREA)
  • Adhesive Tapes (AREA)

Abstract

PURPOSE:To provide an adhesive for an anticorrosive tape having an excellent adhesion which does not require the use of any solvent and heating at the time of using it and can be used in a wide temperature range, by mixing a liquid diene polymer having a hydroxyl group with a polyisocyanate compound and a bituminous substance. CONSTITUTION:A liquid diene polymer (A) having at its terminal a hydroxyl group and having a number-average molecular weight of about 300 - about 25,000 (e.g. butadiene homopolymer or butadiene-styrene copolymer) is mixed with a polyisocyanate compound (B) (e.g. tolylene diisocyanate) and a bituminous substance (C) (e.g. straight asphalt or tar) in such an amount as will provide 1.5-10 equivalents of the isocyanate group contained in the component (B) per equivalent of the hydroxyl group contained in the component (A), to thereby obtain a desired adhesive for an anticorrosive tape. The above-obtained adhesive exhibits an excellent adhesion by merely applying it to an anticorrosive tape made of polyethylene etc., and wrapping the tape around steel pipes etc.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は防食テープ用接着剤に関し、詳しくは使用時に
溶剤、加熱等を必要とせず、しかも使用温度域が広く、
幅広い温度域にわたり接着性の良好な防食テープ用接着
剤に関する。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to an adhesive for anticorrosion tape, and more specifically, it does not require solvents, heating, etc. during use, and has a wide operating temperature range.
This invention relates to an adhesive for anticorrosive tapes that has good adhesion over a wide temperature range.

〔従来技術及び発明が解決しようとする問題点〕従来よ
り、鋼管、殊に水道、ガス等の地下埋設鋼管の表面にテ
ープを巻着して防食を図ることが行なわれている。この
防食テープとしては主にポリエチレンなどのプラスチッ
クが用いられ、その接着剤としてはブチルゴムが用いら
れてきた。しかしながら、このブチルゴJ、を防食テー
プの接着剤として使用するとぎは、ヘンセン。トルエン
等の有′a溶媒に溶解して溶液として用いるか、または
加熱融解させて用いる必要があった。また、特に高温下
では接着性が十分でなく夏期などにおいては剥離現象を
生ずるなど接着性にも改良の余地があるものであった。
[Prior Art and Problems to be Solved by the Invention] Conventionally, corrosion prevention has been carried out by wrapping tape around the surface of steel pipes, especially underground steel pipes for water, gas, etc. pipes. Plastics such as polyethylene have been mainly used for this anticorrosion tape, and butyl rubber has been used as the adhesive. However, when using this Butylgo J as an adhesive for anticorrosion tape, Hensen. It was necessary to use it as a solution by dissolving it in an a-containing solvent such as toluene, or to use it by heating and melting it. In addition, there is room for improvement in adhesion, as the adhesion is insufficient particularly at high temperatures and peeling occurs during summer.

そこで本発明者らは、上記欠点の解消された防食テープ
用接着剤を開発すべく、鋭意検討した結果、特定の物質
を組合せてなる組成物が溶媒、加熱等の必要がなく、接
着剤として良好であることを見出し、本発明を完成する
に至った。
In order to develop an adhesive for anticorrosive tapes that eliminates the above-mentioned drawbacks, the inventors of the present invention have made extensive studies and found that a composition made by combining specific substances does not require solvents, heating, etc., and can be used as an adhesive. It was found that the present invention was successful, and the present invention was completed.

〔問題点を解決するだめの手段〕[Failure to solve the problem]

すなわち、本発明は水酸基含有液状ジエン系重合体、ポ
リイソシアネート化合物および瀝青物質からなる防食テ
ープ用接着剤である。
That is, the present invention is an adhesive for anticorrosive tapes comprising a liquid diene polymer containing hydroxyl groups, a polyisocyanate compound, and a bituminous substance.

本発明において、水酸基含有液状ジエン系重合体として
は分子末端に水酸基を有する数平均分子量が300〜2
5000、好ましくは500〜100 (10の液状ジ
エン系重合体である。これらの液状ジエン系重合体とは
炭素数4〜12のジエン重合体、ジエン共重合体、さら
にはこれらジェ7モ/?−と炭in2〜22のα−オレ
フィン性付加重合性モノマーとの共重合体などがある。
In the present invention, the hydroxyl group-containing liquid diene polymer has a hydroxyl group at the molecular end and has a number average molecular weight of 300 to 2.
5000, preferably 500 to 100 (10).These liquid diene polymers include diene polymers having 4 to 12 carbon atoms, diene copolymers, and furthermore, these diene polymers having 4 to 12 carbon atoms. - and an α-olefinic addition polymerizable monomer having a carbon number of 2 to 22.

具体的にはブタジェンホモポリマー、イソプレンホモポ
リマー、ブタジェン−スチレンコポリマー。
Specifically, butadiene homopolymer, isoprene homopolymer, butadiene-styrene copolymer.

ブタジェン−イソプレンコポリマー、ブタジェン−アク
リロニトリルコポリマー、ブタジェン−2−エチルへギ
シルアクリレートコポリマー、ブタツエン−n−オクク
デシルアクリレートコボリマーなどを例示することがで
きる。
Examples include butadiene-isoprene copolymer, butadiene-acrylonitrile copolymer, butadiene-2-ethylhedyl acrylate copolymer, butatsuene-n-occudecyl acrylate copolymer, and the like.

次にポリイソシアネートとしては、1分子中に2個若し
くはそれ以上のイソシアネート基を有する有機化合物で
あって、上記水酸基含有液状ジエン系重合体の水#基に
対する反応性イソシアネート基を有するものである。こ
のようなポリイソシアネート化合物はよく知られており
、またポリオールとポリイソシアネ−1・を予め反応せ
しめて得られる末端にイソシアネート基を有するプレポ
リマーの形の化合物であってもよい。ポリイソシアネー
ト化合物の例としては、通常の芳香族、脂肪族および指
環族のものをあげることができ、たとえばトリレンジイ
ソシアネート、ヘキサメチレンジイソシアネート、ジフ
ェニルメタンジイソシアネート、液状変性ジフェニルメ
タンジイソシアネート、ポリメチレンポリフェニルイソ
シアネート。
Next, the polyisocyanate is an organic compound having two or more isocyanate groups in one molecule, and has an isocyanate group reactive with the water group of the hydroxyl group-containing liquid diene polymer. Such polyisocyanate compounds are well known, and may be in the form of a prepolymer having isocyanate groups at the ends obtained by reacting a polyol with polyisocyanate-1. Examples of polyisocyanate compounds include the customary aromatic, aliphatic and cyclic ones, such as tolylene diisocyanate, hexamethylene diisocyanate, diphenylmethane diisocyanate, liquid modified diphenylmethane diisocyanate, polymethylene polyphenylisocyanate.

キシリレンジイソシアネート、シクロへキシルジイソシ
アネート、シクロヘキザンフェニレンジイソシアネート
、ナフタリン−1,5−ジイソシアネート、イソプロビ
ルヘンゼンー2.4−ジイソシアネート、ポリプロピレ
ングリコールとトリレンジイソシアネート付加反応物な
どがある。
Examples include xylylene diisocyanate, cyclohexyl diisocyanate, cyclohexanephenylene diisocyanate, naphthalene-1,5-diisocyanate, isopropyrhenzene-2,4-diisocyanate, and addition reaction products of polypropylene glycol and tolylene diisocyanate.

また、瀝青物質としては特に制限なく、ストレードアス
フアル1へ、セミブIIンアスファルト、ブロンアスフ
ァルト、タールあるいはこれらの混合物を例示すること
ができ、好ましくは加工上あまり高温を必要としないス
トレートアスファルトもしくはストレートアスファルト
と他のアスファルトを併用すべきである。
Further, the bituminous substance is not particularly limited, and examples thereof include stranded asphalt, semi-build asphalt, blown asphalt, tar, and mixtures thereof. Preferably, straight asphalt or Straight asphalt and other asphalts should be used together.

本発明の防食テープ用接着剤は上記三成分からなり、配
合量は特に制限はないが、ポリイソシアネート化合物に
含まれるイソシアネート基と水酸基含有液状ジエン系重
合体に含まれる水酸基の当量比がイソシアネート基/水
酸基=1.5〜10.0、好ましくは1.5〜6.0と
なるように選定すべきである。この当量比が1.5未満
であると、接着剤の粘度が高くなって塗布が困難となり
、また10.0を超えると、接着剤の硬化速度が遅くな
り実用上好ましくない。
The adhesive for anticorrosion tape of the present invention consists of the above three components, and although there are no particular restrictions on the amount of the compounded components, the equivalent ratio of the isocyanate groups contained in the polyisocyanate compound to the hydroxyl groups contained in the hydroxyl group-containing liquid diene polymer is such that the isocyanate groups are the same. /hydroxyl group=1.5 to 10.0, preferably 1.5 to 6.0. When this equivalent ratio is less than 1.5, the viscosity of the adhesive becomes high and coating becomes difficult, and when it exceeds 10.0, the curing speed of the adhesive becomes slow, which is not preferred in practice.

また、瀝青物質の配合量は水酸基含有液状ジエン系重合
体100重量部に対して30〜1000重量部、好まし
くは50〜500重量部である。
Further, the amount of the bituminous substance blended is 30 to 1000 parts by weight, preferably 50 to 500 parts by weight, based on 100 parts by weight of the hydroxyl group-containing liquid diene polymer.

本発明の防食テープ用接着剤は原則的には上記三成分か
らなるが、必要により他の添加剤を適宜加えることがで
きる。たとえば、組成物の物性を向上させるために1.
4−ブタンジオール、トリメチロールプロパン、エチレ
ングリコール、ビスフェノールAのエチレンオキシド3
モル付加物、N。
The adhesive for anticorrosion tape of the present invention basically consists of the above three components, but other additives can be added as necessary. For example, in order to improve the physical properties of the composition, 1.
4-butanediol, trimethylolpropane, ethylene glycol, ethylene oxide of bisphenol A 3
Molar adduct, N.

N−ビス(2−ヒドロキシプロピル)アニリンなどを加
えることができる。そのほか粘度調整剤としてジオクチ
ルフタレートなどの可ヅ剤;アロマ系、ナフテン系、パ
ラフィン系の軟化剤を加えたり、粘着力、接着力の調整
のために粘着付与樹脂を加えたり、さらにカーボンブラ
ンク、炭酸カルシウム、クレー、タルクなどの充填剤や
各種安定剤を添加することもできる。ここで粘着付与樹
脂としてはアルギルフェノール樹脂、テルペン樹脂。
N-bis(2-hydroxypropyl)aniline and the like can be added. In addition, softeners such as dioctyl phthalate as viscosity modifiers; aromatic, naphthenic, and paraffinic softeners; tackifying resins to adjust adhesive strength; Fillers such as calcium, clay, and talc and various stabilizers can also be added. Here, the tackifying resin is argylphenol resin or terpene resin.

テルペンフェノール樹脂、キシレンホルムアルデヒド樹
脂、ロジン、水添ロジン、クマロン樹脂。
Terpene phenolic resin, xylene formaldehyde resin, rosin, hydrogenated rosin, coumaron resin.

脂肪族および芳香族石油樹脂などを例示することができ
る。また、貯蔵安定剤としてヘンジイルクロライFなど
、硬化促進剤としてジブチルスズジラウレート、第1ス
ズオクトエートおよびポリエチレンジアミンなど、貯蔵
安定剤として塩化ヘンヅイルなど、耐候性向上のために
老化防止剤、消泡剤としてシリコン化合物などを添加す
ることができる。
Examples include aliphatic and aromatic petroleum resins. In addition, storage stabilizers such as hendyl chloride F, curing accelerators such as dibutyltin dilaurate, stannous octoate, and polyethylene diamine, storage stabilizers such as hendyl chloride, anti-aging agents, and antifoaming agents to improve weather resistance. A silicon compound or the like can be added as an agent.

上記の如き原料を混合、混練することによって本発明の
防食テープ用接着剤が得られる。混練は通常行なわれて
いる方法により行なえばよく、たとえばバンバリーミキ
サ−などを用いて0〜120℃、好ましくは10〜90
℃で0.5〜48時間、好ましくは6〜16時間溶融混
練することによって行なうことができる。好ましくは水
酸基含有液状ジエン系重合体と瀝青物質を加熱攪拌後、
冷却し、次いで加熱溶融したポリイソシアネート化合物
を加えて混練したのち冷却することにより本発明の防食
テープ用接着剤が得られる。
The adhesive for anticorrosion tape of the present invention can be obtained by mixing and kneading the above raw materials. Kneading may be carried out by a commonly used method, for example using a Banbury mixer or the like at 0 to 120°C, preferably 10 to 90°C.
This can be carried out by melt-kneading at a temperature of 0.5 to 48 hours, preferably 6 to 16 hours. Preferably, after heating and stirring the hydroxyl group-containing liquid diene polymer and the bituminous material,
The adhesive for anticorrosion tape of the present invention is obtained by cooling, then adding and kneading a heated and melted polyisocyanate compound, and then cooling.

このようにして得られる防食テープ用接着剤は湿気硬化
性を有するプレポリマーであって、空気中の湿気により
ウレア結合を生成してポリマー化して硬化物となると考
えられる。
The adhesive for anticorrosion tape thus obtained is a moisture-curable prepolymer, and is thought to form a urea bond due to moisture in the air and polymerize into a cured product.

〔発明の効果〕〔Effect of the invention〕

この防食テープ用接着剤はポリエチレン等からなる防食
テープに何ら特別な処理を施すことなく単に塗布するだ
けで鋼管等に巻着した際に良好な接着性を示すものであ
る。この塗布において、本発明の接着剤はヘンゼン、ト
ルエンの如き有機溶媒を使用する必要がなく、また加熱
熔融する必要もなく、作業性に優れている。得られた硬
化体の接着力は大きく、しかも低温から高温までの幅広
い温度域にわたり強固な接着性を有している。
This anticorrosion tape adhesive exhibits good adhesion when wrapped around a steel pipe or the like by simply applying it to an anticorrosion tape made of polyethylene or the like without any special treatment. In this application, the adhesive of the present invention does not require the use of organic solvents such as Hensen or toluene, nor does it require heating and melting, and is excellent in workability. The obtained cured product has high adhesive strength and has strong adhesive properties over a wide temperature range from low to high temperatures.

したがって、本発明の防食テープ用接着剤はガス、水道
などの鋼管等の防食テープの接着剤として極めて有用で
ある。
Therefore, the adhesive for anticorrosive tapes of the present invention is extremely useful as an adhesive for anticorrosive tapes for steel pipes for gas, water, etc.

〔実施例〕〔Example〕

次に、本発明を実施例によりさらに詳しく説明する。 Next, the present invention will be explained in more detail with reference to Examples.

実施例1 末端に水酸基を有する液状ポリブタジェン(出光石油科
学側製、  rPoly bd R−45HTj 、水
酸基含有io、 79 meq/ g 、数平均分子i
i2800)100gおよびストレートアスファルト(
針入度150/200)  452.6 gを17!セ
パラブルフラスコに入れ、l ts* Hg、80°C
にて1時間加熱脱水を行なった。その後、40°Cまで
冷却し、60°Cに加熱熔融した4、4′−ジフェニル
メタンジイソシアネー)31.4gを加え、激しく攪拌
し1時間、60℃にて保持した。次いで、80℃に加熱
して3時間攪拌したのちジブチルスズジラウレート0.
5gを添加し、さらに15分間攪拌後、冷却して防水シ
ート用接着剤を得た。このものは黒色、粘度1200ポ
イズ/25℃、イソシアネート基含量0.9重量%であ
った。
Example 1 Liquid polybutadiene having a hydroxyl group at the end (manufactured by Idemitsu Petroleum Science Co., Ltd., rPoly bd R-45HTj, hydroxyl group-containing io, 79 meq/g, number average molecule i
i2800) 100g and straight asphalt (
Penetration 150/200) 452.6 g 17! Place in a separable flask, l ts* Hg, 80°C.
Dehydration was performed by heating for 1 hour. Thereafter, the mixture was cooled to 40°C, and 31.4 g of 4,4'-diphenylmethane diisocyanate heated and melted at 60°C was added, stirred vigorously, and maintained at 60°C for 1 hour. Next, after heating to 80°C and stirring for 3 hours, dibutyltin dilaurate 0.
After adding 5 g of the mixture and stirring for another 15 minutes, the mixture was cooled to obtain an adhesive for a waterproof sheet. This product was black, had a viscosity of 1200 poise/25°C, and had an isocyanate group content of 0.9% by weight.

防食テープにこの接着剤を塗布し、鋼板に温度25℃、
湿度60%にて1週間養生した。この際の180°ビ一
ル接着強度を測定した。結果を第1表に示す。また、4
0℃における180°ビ一ル接着強度を併せて第1表に
示す。
Apply this adhesive to anti-corrosion tape and heat it to a steel plate at a temperature of 25℃.
It was cured for one week at a humidity of 60%. At this time, the 180° vinyl adhesive strength was measured. The results are shown in Table 1. Also, 4
Table 1 also shows the 180° vinyl adhesive strength at 0°C.

比較例 ブチルゴム系粘着剤(ベンゼン含有量 30重量%)を
ロールコータ−によりポリエチレンテープおよびポリプ
ロピレンテープ上に塗布した後、乾燥し、この粘着テー
プを銅板に圧着し、その180’ビ一ル接着強度を測定
した。結果を第1表に示す。
Comparative Example A butyl rubber adhesive (benzene content: 30% by weight) was applied onto polyethylene tape and polypropylene tape using a roll coater, dried, and the adhesive tape was pressed onto a copper plate to determine its 180' vinyl adhesive strength. was measured. The results are shown in Table 1.

Claims (2)

【特許請求の範囲】[Claims] (1)水酸基含有液状ジエン系重合体、ポリイソシアネ
ート化合物および瀝青物質からなる防食テープ用接着剤
(1) An adhesive for anticorrosion tape comprising a hydroxyl group-containing liquid diene polymer, a polyisocyanate compound, and a bituminous substance.
(2)ポリイソシアネート化合物の配合量がイソシアネ
ート基/水酸基(当量比)=1.5〜10.0となる量
である特許請求の範囲第1項記載の接着剤。
(2) The adhesive according to claim 1, wherein the amount of the polyisocyanate compound is such that the isocyanate group/hydroxyl group (equivalent ratio) is 1.5 to 10.0.
JP1357785A 1985-01-29 1985-01-29 Adhesive for anticorrosive tape Granted JPS61174282A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1357785A JPS61174282A (en) 1985-01-29 1985-01-29 Adhesive for anticorrosive tape

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1357785A JPS61174282A (en) 1985-01-29 1985-01-29 Adhesive for anticorrosive tape

Publications (2)

Publication Number Publication Date
JPS61174282A true JPS61174282A (en) 1986-08-05
JPH0361713B2 JPH0361713B2 (en) 1991-09-20

Family

ID=11837019

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1357785A Granted JPS61174282A (en) 1985-01-29 1985-01-29 Adhesive for anticorrosive tape

Country Status (1)

Country Link
JP (1) JPS61174282A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0843761A1 (en) * 1995-07-10 1998-05-27 Interface, Inc. Urethane-modified bitumen sheet material and method for protective moisture barrier
WO2000011111A2 (en) * 1998-08-19 2000-03-02 Urecoats International, Inc. Bituminous polyurethane interpenetrating elastomeric network compositions

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5258U (en) * 1975-06-19 1977-01-05
JPS539778A (en) * 1976-07-13 1978-01-28 Takeda Chem Ind Ltd Preparation of 5-fluorouracil derivativds
JPS5711394U (en) * 1980-06-25 1982-01-21
JPS57182372A (en) * 1981-05-06 1982-11-10 Idemitsu Kosan Co Ltd Self-adhesive composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55154593A (en) * 1979-05-23 1980-12-02 Osaka Soda Co Ltd Diaphragm type alkali chloride electrolytic bath

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5258U (en) * 1975-06-19 1977-01-05
JPS539778A (en) * 1976-07-13 1978-01-28 Takeda Chem Ind Ltd Preparation of 5-fluorouracil derivativds
JPS5711394U (en) * 1980-06-25 1982-01-21
JPS57182372A (en) * 1981-05-06 1982-11-10 Idemitsu Kosan Co Ltd Self-adhesive composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0843761A1 (en) * 1995-07-10 1998-05-27 Interface, Inc. Urethane-modified bitumen sheet material and method for protective moisture barrier
EP0843761A4 (en) * 1995-07-10 1999-12-22 Interface Inc Urethane-modified bitumen sheet material and method for protective moisture barrier
WO2000011111A2 (en) * 1998-08-19 2000-03-02 Urecoats International, Inc. Bituminous polyurethane interpenetrating elastomeric network compositions
WO2000011111A3 (en) * 1998-08-19 2000-06-02 Urecoats International Inc Bituminous polyurethane interpenetrating elastomeric network compositions
US6271305B1 (en) * 1998-08-19 2001-08-07 Urecoats Technologies, Inc. Bituminous polyurethane interpenetrating elastomeric network compositions as coatings and sealants for roofing and other applications

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