JPH01110581A - Reactive tacky agent composition - Google Patents

Reactive tacky agent composition

Info

Publication number
JPH01110581A
JPH01110581A JP62266899A JP26689987A JPH01110581A JP H01110581 A JPH01110581 A JP H01110581A JP 62266899 A JP62266899 A JP 62266899A JP 26689987 A JP26689987 A JP 26689987A JP H01110581 A JPH01110581 A JP H01110581A
Authority
JP
Japan
Prior art keywords
acrylic
room temperature
solid
meth
ordinary temperature
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
JP62266899A
Other languages
Japanese (ja)
Other versions
JP2739152B2 (en
Inventor
Kiyoshi Ono
清 小野
Yoshio Kishimoto
芳男 岸本
Tetsuto Sato
佐藤 哲人
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.)
Nichiban Co Ltd
Original Assignee
Nichiban 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 Nichiban Co Ltd filed Critical Nichiban Co Ltd
Priority to JP62266899A priority Critical patent/JP2739152B2/en
Priority to EP88117576A priority patent/EP0313071B1/en
Priority to DE8888117576T priority patent/DE3880427T2/en
Publication of JPH01110581A publication Critical patent/JPH01110581A/en
Priority to US08/066,929 priority patent/US5326605A/en
Application granted granted Critical
Publication of JP2739152B2 publication Critical patent/JP2739152B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a reactive tacky agent composition, consisting of a saturated polyester resin which is a solid at ordinary temperature, etc., (meth)acrylic urethane monomer having a specific viscosity at ordinary temperature, etc., having moderate tackiness at ordinary temperature and curable with light, etc., to provide strong adhesive force. CONSTITUTION:A reactive tacky agent composition, obtained by dissolving (A) one or more of a saturated polyester resin, acrylic rubber, acrylic elastomer, polybutadiene and acrylic tacky agent and (B) one or more of an acrylic or methacrylic urethane monomer, oligomer and other (meth)acrylic monomers and oligomers which are a solid at ordinary temperature having >=10<2>cP viscosity at ordinary temperature in a solvent and drying the solvent and suitable as sealing media. Furthermore, one or more of photo- or thermosetting catalyst or further magnetic substance, electric conductor, fluorescent substance, etc., are preferably contained in the above-mentioned components.

Description

【発明の詳細な説明】 此の発明は、熱や電離放射線によって硬化する反応性粘
着剤組成物に関するものである。更に詳しくは、この組
成物は初めは粘着力があるが、熱あるいは光(二より硬
化して接着力を生じる反応性粘着剤組成物である。
DETAILED DESCRIPTION OF THE INVENTION This invention relates to a reactive adhesive composition that is cured by heat or ionizing radiation. More specifically, this composition is a reactive pressure-sensitive adhesive composition that initially has adhesive strength but is cured by heat or light (secondary heat or light) to generate adhesive strength.

粘着テープは常温で粘着性を有しており、何の予備操作
もなしく一目的物に貼付できる。しかも、貼り直しが可
能であるという利点から多方面で使用されている。しか
し粘着テープにはその接着力は一般的に接着剤に較べて
弱いという欠点がある。
Adhesive tape is sticky at room temperature and can be attached to a single object without any preliminary operations. Moreover, it is used in many fields because of its ability to be reattached. However, adhesive tapes have the disadvantage that their adhesive strength is generally weaker than that of adhesives.

また通常、テープ基材に粘着剤を塗布したものがテープ
となっているため、複雑な形状の部位、例えば段差のあ
る部位、へこんだり、つきだしたりしている部位には、
基材のもつ厚み、硬さや腰等のため隙なく貼り付けるこ
とが不可能である。また粘着テープは耐水性、耐溶剤性
や耐熱性にも問題がある。
Also, since the tape is usually made by applying an adhesive to the tape base material, it can be used on areas with complex shapes, such as areas with steps, dents, or protrusions.
Due to the thickness, hardness, stiffness, etc. of the base material, it is impossible to paste it without gaps. Adhesive tapes also have problems with water resistance, solvent resistance, and heat resistance.

一方、塗料、接着剤、シーラー剤などは複雑な形状、曲
面、穴、突起、段差、隙間等に対して適応可能であり、
硬化反応も利用できるため、耐水性、耐溶剤性、耐熱性
を向上させるのに有利である。しかし、これらは使用前
に硬化剤を混ぜ合わせたりする前処理が必要であるうえ
に、通常は溶剤に°含むゾル状あるいはペースト状であ
るため、その取り扱いは手で直接触れられなかったり、
水平な面の上の容器中でないといけないため煩わしい。
On the other hand, paints, adhesives, sealants, etc. can be applied to complex shapes, curved surfaces, holes, protrusions, steps, gaps, etc.
Since a curing reaction can also be utilized, it is advantageous for improving water resistance, solvent resistance, and heat resistance. However, these require pretreatment such as mixing a hardening agent before use, and because they are usually in the form of a sol or paste containing a solvent, they cannot be handled directly by hand.
It is cumbersome because it has to be in a container on a horizontal surface.

又、施工時の流れ、たれ、しぶき(二よる目的個所以外
の部分への汚染を注意しなければならないし、−度汚染
をした場合の除去は極めて繁雑であり、不可能な場合も
多くある。
In addition, care must be taken to avoid contamination of areas other than the intended area due to construction flow, drips, and spray (2), and removal of contamination is extremely complicated and often impossible. .

以上の状況を鑑み、粘着剤の良いところと、塗料、接着
剤、シーラーの良いところだけを兼ね持ち、これら欠点
を取り除いたものを得るべく、鋭意努力した結果、本発
明を完成するに至った。本発明で発明されたものは、何
ら予備操作なしに目的物に貼付し、硬化が終了するまで
固定できる粘着力があり、そのうえ、−度貼付に失敗し
ても何らの汚染もなく貼り直しが可能で、何らかの手段
で硬化した後は、塗料、接着剤、シーラー剤、保護被膜
形成剤、もしくは有機粉末のバインダー剤と同様の品質
・性能をもつものである。硬化方法は目的・工程・顔料
の性質・経済性(=含ませ、熱、光、電離放射線が使用
できる。
In view of the above circumstances, we have worked diligently to create a product that combines the advantages of adhesives, paints, adhesives, and sealers, and eliminates these drawbacks, and as a result we have completed the present invention. . The product invented by the present invention has adhesive strength that allows it to be applied to the target object without any preliminary operation and fixed until curing is completed, and furthermore, even if pasting fails, it can be reapplied without any contamination. If possible, and after curing by some means, it has the same quality and performance as a paint, adhesive, sealer, protective film forming agent, or organic powder binder. The curing method depends on the purpose, process, properties of the pigment, and economic efficiency (= impregnation, heat, light, and ionizing radiation can be used.

従来までに、熱硬化性シートやホットメルト接着剤等は
既に市販されているが、常態で粘着力があり、硬化する
ものは未だない。
Until now, thermosetting sheets, hot melt adhesives, and the like have already been commercially available, but there are still none that are adhesive and harden under normal conditions.

本発明は、粘度が常温で102CpS以上であるアクリ
ルウレタンモノマー若しくはオリゴマーで形成される硬
化性樹脂と凝集力があり常温では固体ァあ、□。! 2
 #騙W7尖7゛にLz”ニア”AT’アクリル粘着剤
から選ばれる少なくとも一種を含有していることを特徴
としている。これらの組み合わせから常温で適当な粘着
特性、すなわち初期のタック、保持力、粘着力をもち、
熱、光、電離放射線で容易に硬化することができ、硬化
後は極めて強靭なあるいは弾力性のある物性を有するも
のを得ることができた。本発明の特徴は、低分子量の粘
着付与樹脂を全く使用せずに粘着性を出しているところ
である。従って、硬化後の耐溶剤性、耐熱性が優れてい
る。上記のアクリル粘着剤はアクリル系重合体、アクリ
ル系共重合体等である。
The present invention is a curable resin formed from an acrylic urethane monomer or oligomer that has a viscosity of 102 CpS or more at room temperature and has cohesive force and is solid at room temperature. ! 2
It is characterized by containing at least one type selected from Lz "Near"AT' acrylic adhesive on the tip 7 of #DameW7. From these combinations, it has suitable adhesive properties at room temperature, namely initial tack, holding power, and adhesion.
It can be easily cured by heat, light, or ionizing radiation, and after curing, it was possible to obtain a product with extremely strong or elastic physical properties. A feature of the present invention is that it achieves tackiness without using any low molecular weight tackifier resin. Therefore, it has excellent solvent resistance and heat resistance after curing. The above-mentioned acrylic pressure-sensitive adhesive is an acrylic polymer, an acrylic copolymer, or the like.

反応性(メタ)アクリレート樹脂のモノマー、オリゴマ
ー、低分子量物では、常温ではたとえ固体であっても凝
集力に乏しい。また、飽和ポリエステル樹脂、ポリブタ
ジェン樹脂、アクリルエラストマー、アクリルゴムはそ
れ自身が反応性アクリレートのように反応しない。発明
者等はこの2種類の樹脂を組み合わせることによって常
態で粘着力のある硬化性の組成物を得ることに成功した
Monomers, oligomers, and low molecular weight reactive (meth)acrylate resins have poor cohesive force at room temperature even if they are solid. Furthermore, saturated polyester resins, polybutadiene resins, acrylic elastomers, and acrylic rubbers themselves do not react like reactive acrylates. By combining these two types of resins, the inventors succeeded in obtaining a curable composition that is adhesive under normal conditions.

本発明に使用する反応性樹脂は、常温の粘度が/θ2c
ps以上の液体、もしくは固体であり、一方の凝集力の
ある樹脂はガラス転移点が室温以下である常態で固体の
樹脂である。これらの樹脂を溶融あるいは溶解により均
一に分散あるいは相溶させて本発明の反応性粘着剤が得
られる。得られたものは常温では流動性がなく、適当の
粘着性と凝集力をもつため、あらゆる形態で供給できる
。例えば、ひも状、ペレット状、シート状、ブロック状
である。
The reactive resin used in the present invention has a viscosity of /θ2c at room temperature.
A resin having a cohesive force is a liquid or a solid having a glass transition point of less than or equal to room temperature and is normally solid. The reactive pressure-sensitive adhesive of the present invention can be obtained by uniformly dispersing or dissolving these resins by melting or dissolving them. The obtained product has no fluidity at room temperature and has appropriate adhesiveness and cohesive strength, so it can be supplied in any form. For example, they are string-like, pellet-like, sheet-like, and block-like.

また硬化法として上記の組成物の中に適当な光増感剤等
の触媒を加えることで、熱でも電離放射線でも硬化でき
、熱の場合は硬化温度を適当に調節する。前記の触媒を
加えた組成物を例えば、剥離紙上に延展して反応性粘着
剤のシートをつくり、該シートを被着体に貼付した後、
剥離紙を剥がして熱をかければ、厚ぬりのコーティング
ができることになる。また鉄板の継目や凹部に適用すれ
ばシーラーやパテの代用となる。
Further, as a curing method, by adding a suitable catalyst such as a photosensitizer to the above-mentioned composition, it can be cured by heat or ionizing radiation, and in the case of heat, the curing temperature is appropriately adjusted. For example, the composition to which the catalyst has been added is spread on a release paper to make a sheet of reactive adhesive, and after applying the sheet to an adherend,
If you peel off the release paper and apply heat, you'll get a thick coating. It can also be used as a substitute for sealers and putty when applied to the joints and recesses of iron plates.

この反応性粘着剤はシーリング剤として使えば、これま
でガンを用いては困難であったところにも、手軽にシー
リングを行うことができる。また、施工(ニー度失敗し
ても、きれいに剥がせるため汚染がない等作業性は大幅
に改善される。以下実施例によって説明する。
By using this reactive adhesive as a sealant, it is possible to easily seal areas that were previously difficult to apply using a gun. In addition, even if the application fails, the workability is greatly improved, as it can be removed cleanly and there is no contamination.Examples will be explained below.

〔実施例/〕〔Example/〕

飽和ポリエステル LP−02,27部部(日本合成)
         種1部以下同じ)ウレタンアクリレ
ート ビスコート ♂7.2 3部部(大阪有機) インブチルパーオキサイド     7部を固形分が3
0部程度になるよう(ニトルエン)二溶かした。この溶
液を剥離紙で作った箱に流し込み、溶剤を乾燥させて!
00μmの粘着フィルムを作った。得られたフィルムを
シーリング剤として使用するため、鉄板の継目(=貼り
、剥離紙を剥がした後、750℃で、30分加熱硬化さ
せた。
Saturated polyester LP-02, 27 parts (Nippon Gosei)
(same as below 1 part seed) Urethane acrylate viscoat ♂7.2 3 parts (Osaka Organic) Inbutyl peroxide 7 parts with a solid content of 3
Two parts (nitoluene) were dissolved so that the amount was about 0 parts. Pour this solution into a box made of release paper and let the solvent dry!
A 00 μm adhesive film was made. In order to use the obtained film as a sealant, it was pasted on the seam of iron plates, and after peeling off the release paper, it was heated and cured at 750° C. for 30 minutes.

上記組成物は硬化油は粘着性があり、再貼りが可能であ
った。また硬化時C二組酸物は溶けてシートの角がとれ
鉄板の隙間をうめた。硬化したちのは沸騰水に7時間浸
けても変化しなかった。
The hydrogenated oil in the above composition was sticky and could be reapplied. Also, during curing, the C2 acid melted, the corners of the sheet came off, and the gaps between the iron plates were filled. The hardened material did not change even after being soaked in boiling water for 7 hours.

〔実施例2〕 実施例/において得られた5008mの粘着フィルムを
打ち抜き加工により、内径乙mに3のドーナツツ型(=
打ち抜いた。これを外径がjwtsBボルトにワッシャ
ーのかわりとして用い、ナツトで鉄板に締め付けたこの
後、760℃、20分で加熱硬化させた。
[Example 2] The 5008 m long adhesive film obtained in Example 2 was punched to form a donut shape (=3) with an inner diameter of m.
Punched out. This was used as a washer for a bolt with an outer diameter of JWTS B, and was tightened to an iron plate with a nut, and then heated and hardened at 760° C. for 20 minutes.

組成物は溶融硬化し、ゆるみどめ、もしくは耐水若しく
は防水シーラーとして適当であるとわかった。
The compositions were found to be melt hardening and suitable as a loosening or waterproof sealer.

〔実施例3〕 飽和ポリエステル パイロン20θ  20部ウレタン
アクリレート アロニツクス M−110030部(東
亜合成■) シリカ微粉末 アエロジル R−2722部部(日本ア
エロジル■) 顔料 チタン白 平均粒径θ、!μm 2部部インブチ
ルパーオキサイド     /部上記(:記した原料を
ニーダ−により混合し、自動車の車体からとったエンブ
レムのシリコンゴム型へ射出成形機を使用して流し込ん
だ。冷えた後エンブレム成形体をシリコンゴムの型から
取り出した。このエンブレム成形体を自動車の車体(−
貼り、790℃、20分の条件で加熱硬化させたところ
、エンブレム成形体は硬化し車体に強固(;接着した。
[Example 3] Saturated polyester Pylon 20θ 20 parts Urethane acrylate Aronix M-1100030 parts (Toagosei ■) Silica fine powder Aerosil R-2722 parts (Nippon Aerosil ■) Pigment Titanium white Average particle size θ,! μm 2 parts Inbutyl peroxide / part Above (: The raw materials listed above were mixed in a kneader and poured into a silicone rubber mold for an emblem taken from a car body using an injection molding machine. After cooling, the emblem was molded. The body was taken out from the silicone rubber mold.This emblem molded body was molded into a car body (-
When the emblem molded product was pasted and cured by heating at 790° C. for 20 minutes, it was cured and firmly adhered to the vehicle body.

またこの上より塗料を吹きかけたところ密着も一層良好
(二なった。
Also, when I sprayed paint on top of this, the adhesion was even better.

父上記の配合原料中(:螢光体を混合し、同じようにエ
ンブレムの型をしたti体を作って車体に貼り付けた。
My father mixed the above-mentioned ingredients with the phosphor, made a Ti body in the same emblem shape, and pasted it on the car body.

貼られたエンブレムは暗くすると螢光を発光し、文字が
浮かび上がった。
When the emblem was pasted on, it emitted fluorescent light when it was darkened, and the letters appeared.

〔実施例ダ〕[Example D]

実施例/により得られたシートについて、あらかじめシ
ーリングを施す部位の形をかたどり、シートを打ち抜き
加工した。これにより、シーリングを施す作業性は更に
改良することができた。
The sheet obtained in Example 1 was punched out in the shape of the area to be sealed. This made it possible to further improve the workability of sealing.

〔実施例!〕〔Example! ]

飽和ポリエステル LP−022,gO部(日本合成) フレタンアクリレート樹脂 アートレジン UN−9000(機上工業)  グθ部
顔料 チタン白 平均粒径4tOμm   30部パー
ロイル IPP  (日本浦脂)    2部上記の配
合を実施例/に示したと同様にトルエン溶液を作り、形
に流し込んで厚さ200μmのフィルムを作った。これ
を鉄板の上(=貼り、硬化させて鉄板との密着性を調べ
た。
Saturated polyester LP-022, gO part (Nippon Gosei) Frethane acrylate resin art resin UN-9000 (Kigami Kogyo) Gu θ part Pigment Titanium white Average particle size 4tOμm 30 parts Perloyl IPP (Nippon Urashi) 2 parts Above formulation A toluene solution was prepared in the same manner as shown in Example 1, and poured into a mold to form a film with a thickness of 200 μm. This was pasted on an iron plate, allowed to harden, and its adhesion to the iron plate was examined.

鉄板上で硬化したフィルムは塗料の基板目試験で10θ
//θOの密着性があることがわかった。
The film cured on the iron plate has 10θ in the paint board test.
It was found that there was an adhesion of //θO.

〔実施例6〕 アクリルゴム  ドアアクロン PS−210+θ部(
東亜ペイント) アクリレート S−/22      90部(日本油
脂) tertブチルパーベンゾエート    3部を固形分
濃度が20チ程度になるように酢酸エチルC二とかし、
厚みが25μmのポリエステルフィルム ティングした。このテープを紙の上(二貼り、/りθ℃
のアイロンを2秒あてた。
[Example 6] Acrylic rubber door Acron PS-210 + θ part (
Toa Paint) Acrylate S-/22 90 parts (Nippon Oil & Fats) 3 parts of tert-butyl perbenzoate were dissolved with ethyl acetate C to a solid concentration of about 20%,
A polyester film having a thickness of 25 μm was used. Place this tape on the paper (double paste, / θ℃
I applied the iron for 2 seconds.

/グ0℃のアイロンを2秒あてると粘着剤は硬化して、
紙(=密着した。テープが冷えた後、ポリエステルフィ
ルムを剥がすと硬化した粘着剤は紙に残り耐粘着性の被
膜ができた。
The adhesive will harden by applying an iron at 0°C for 2 seconds.
Paper (= adhered to the tape. After the tape had cooled, the polyester film was peeled off and the hardened adhesive remained on the paper, creating a tack-resistant film.

〔実施例7〕 アクリルゴム ドアアクロン P S −2/ 0 6
0部(東亜ペイント) アクリレート UAS−1090部 (山陽国栄パルプ) イルガキュア 907      3部上記の配合を酢
酸エチルに溶かし、厚さが2よμmのポリエステルフィ
ルムの上にコーティングした。このテープを銅板の上に
貼り、♂θW/iの高圧水銀ランプで紫外線を照射した
。粘着面は硬化して、銅板の上に貼り付いた。この膜の
電気抵抗は、1013Ω口であった。
[Example 7] Acrylic rubber Door Acron PS-2/06
0 parts (Toa Paint) Acrylate UAS-1090 parts (Sanyo Kokuei Pulp) Irgacure 907 3 parts The above formulation was dissolved in ethyl acetate and coated on a polyester film having a thickness of 2 μm. This tape was pasted on a copper plate and irradiated with ultraviolet rays using a ♂θW/i high-pressure mercury lamp. The adhesive surface hardened and stuck to the copper plate. The electrical resistance of this film was 1013Ω.

〔実施例♂〕[Example ♂]

アクリル系粘着剤        60部アクリレート
 NKエステルU−4tHA    4tQ部(新中村
) パーロイル IPP  (日本油脂)    /部上記
の原料を酢酸エチルに溶し、剥離処理されたPETフィ
ルムにコーティングして両面テープを作った。この両面
テープを2板の金属板の間に貼り付け、750℃、20
分で硬化させ、剪断接着力を測定した。剪断接着力は/
 00 Kg/c、であった。
Acrylic adhesive 60 parts Acrylate NK ester U-4tHA 4tQ part (Shin Nakamura) Perloil IPP (NoF) / part The above raw materials were dissolved in ethyl acetate and coated on a release-treated PET film to make a double-sided tape. Ta. Paste this double-sided tape between two metal plates and heat at 750℃ for 20 minutes.
The adhesive was cured for 1 minute and the shear adhesion was measured. The shear adhesive strength is /
00 Kg/c.

〔実施例ワ〕[Example wa]

飽和ポリエステル LP−θ114t70部アクリレー
ト樹脂 C−9034t30部(サートマー) パーロイル IPP  (日本油脂)    2部上記
の原料を酢酸エチルに溶かし、デコレーションシートの
裏側にコーティングした。これを鉄板に貼付し、赤外線
のヒーターで7.0分間温めて接着させた。
Saturated polyester LP-θ114t 70 parts Acrylate resin C-9034t 30 parts (Sartomer) Perloyl IPP (NOF) 2 parts The above raw materials were dissolved in ethyl acetate and coated on the back side of the decoration sheet. This was pasted on an iron plate and heated with an infrared heater for 7.0 minutes to bond it.

〔実施例10〕 実施例7に示した組成物を厚さが70μmの銅のホイル
(=塗工した。そして、スリッターにより幅<1rrs
に裁断し、まきはじめにリード線を取りつけて、径7イ
ンチ芯に700θm巻き、厚に巻き終わり(=リード線
をつけた。これを加熱オーブンに入れ、750℃、90
分で加熱硬化させて、薄形のコイルを作った。
[Example 10] The composition shown in Example 7 was coated on a copper foil with a thickness of 70 μm.
Attach a lead wire at the beginning of winding, wrap it 700θm around a 7-inch diameter core, and finish winding thickly (= the lead wire is attached.) Place this in a heating oven at 750℃, 90℃.
I made a thin coil by heating and curing it in minutes.

特許出願人  ニチバン株式会社 手続補正書 昭和に3年7 月79日Patent applicant: Nichiban Co., Ltd. Procedural amendment July 79, 3rd year of Showa era

Claims (1)

【特許請求の範囲】 1 常温で固体である飽和ポリエステル樹脂、アクリル
ゴム、アクリルエラストマー、ポリブタジエンおよびア
クリル粘着剤から選ばれる少なくとも1種と、常温で粘
度が10^2cps以上の(メタ)アクリルウレタンモ
ノマー、オリゴマーおよびその他の低分子量物から選ば
れる少なくとも1種を含有する反応性粘着剤組成物。 2 常温で固体である飽和ポリエステル樹脂、アクリル
ゴム、アクリルエラストマー、ポリブタジエンおよびア
クリル粘着剤から選ばれる少なくとも1種と、常温で粘
度が10^2cps以上の(メタ)アクリルウレタンモ
ノマー、オリゴマーおよびその他の低分子量物から選ば
れる少なくとも1種と光若しくは熱硬化触媒を含有する
反応性粘着剤組成物。 3 常温で固体である飽和ポリエステル樹脂、アクリル
ゴム、アクリルエラストマー、ポリブタジエンおよびア
クリル粘着剤から選ばれる少なくとも1種と、常温で粘
度が10^2cps以上の(メタ)アクリルウレタンモ
ノマー、オリゴマーおよびその他の低分子量物から選ば
れる少なくとも1種と、硬化触媒と、磁性体、導電体、
誘電体、螢光体、顔料、有機樹脂微粉末、無機物粉末及
び金属粉末から選ばれる少なくとも1種を含有する反応
性粘着剤組成物。
[Scope of Claims] 1. At least one member selected from saturated polyester resin, acrylic rubber, acrylic elastomer, polybutadiene, and acrylic adhesive that is solid at room temperature, and (meth)acrylic urethane monomer having a viscosity of 10^2 cps or more at room temperature. , oligomers and other low molecular weight substances. 2 At least one selected from saturated polyester resins, acrylic rubbers, acrylic elastomers, polybutadiene, and acrylic adhesives that are solid at room temperature, and (meth)acrylic urethane monomers, oligomers, and other low-temperature viscosity of 10^2 cps or more at room temperature. A reactive pressure-sensitive adhesive composition containing at least one kind selected from molecular weight substances and a photo- or heat-curing catalyst. 3 At least one selected from saturated polyester resins, acrylic rubbers, acrylic elastomers, polybutadiene, and acrylic adhesives that are solid at room temperature, and (meth)acrylic urethane monomers, oligomers, and other low-temperature viscosity of 10^2 cps or more at room temperature. at least one selected from molecular weight substances, a curing catalyst, a magnetic material, an electrical conductor,
A reactive adhesive composition containing at least one selected from dielectrics, fluorescent materials, pigments, organic resin fine powders, inorganic powders, and metal powders.
JP62266899A 1987-10-22 1987-10-22 Reactive adhesive composition Expired - Fee Related JP2739152B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP62266899A JP2739152B2 (en) 1987-10-22 1987-10-22 Reactive adhesive composition
EP88117576A EP0313071B1 (en) 1987-10-22 1988-10-21 Reactive pressure sensitive adhesive composition, sealer tape, sheet or molding by use thereof
DE8888117576T DE3880427T2 (en) 1987-10-22 1988-10-21 REACTIVE ADHESIVE ADHESIVE
US08/066,929 US5326605A (en) 1987-10-22 1993-05-26 Reactive pressure sensitive adhesive composition, sealer tape, sheet or molding by use thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62266899A JP2739152B2 (en) 1987-10-22 1987-10-22 Reactive adhesive composition

Publications (2)

Publication Number Publication Date
JPH01110581A true JPH01110581A (en) 1989-04-27
JP2739152B2 JP2739152B2 (en) 1998-04-08

Family

ID=17437204

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62266899A Expired - Fee Related JP2739152B2 (en) 1987-10-22 1987-10-22 Reactive adhesive composition

Country Status (1)

Country Link
JP (1) JP2739152B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5084346A (en) * 1988-04-30 1992-01-28 Nichiban Company Limited Sealer material

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1178098A4 (en) 2000-02-02 2004-12-15 Honda Motor Co Ltd String type sealing material

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4826232A (en) * 1971-08-09 1973-04-06
JPS50140538A (en) * 1974-02-19 1975-11-11
JPS5428384A (en) * 1977-08-05 1979-03-02 Toyobo Co Ltd Urethane-modified acrylate resin composition
JPS59176370A (en) * 1983-03-28 1984-10-05 Nitto Electric Ind Co Ltd Pressure-sensitive adhesive composition
JPS6013868A (en) * 1983-07-05 1985-01-24 Showa Highpolymer Co Ltd Pressure-sensitive adhesive composition having anaerobic curability
JPS63210182A (en) * 1987-02-26 1988-08-31 Sanyo Chem Ind Ltd Pressure-sensitive adhesive composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4826232A (en) * 1971-08-09 1973-04-06
JPS50140538A (en) * 1974-02-19 1975-11-11
JPS5428384A (en) * 1977-08-05 1979-03-02 Toyobo Co Ltd Urethane-modified acrylate resin composition
JPS59176370A (en) * 1983-03-28 1984-10-05 Nitto Electric Ind Co Ltd Pressure-sensitive adhesive composition
JPS6013868A (en) * 1983-07-05 1985-01-24 Showa Highpolymer Co Ltd Pressure-sensitive adhesive composition having anaerobic curability
JPS63210182A (en) * 1987-02-26 1988-08-31 Sanyo Chem Ind Ltd Pressure-sensitive adhesive composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5084346A (en) * 1988-04-30 1992-01-28 Nichiban Company Limited Sealer material

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