JPH0734052A - Pressure-sensitive adhesive and adhesive sheet using the same - Google Patents

Pressure-sensitive adhesive and adhesive sheet using the same

Info

Publication number
JPH0734052A
JPH0734052A JP20111493A JP20111493A JPH0734052A JP H0734052 A JPH0734052 A JP H0734052A JP 20111493 A JP20111493 A JP 20111493A JP 20111493 A JP20111493 A JP 20111493A JP H0734052 A JPH0734052 A JP H0734052A
Authority
JP
Japan
Prior art keywords
adhesive
group
pressure
sensitive adhesive
meth
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
JP20111493A
Other languages
Japanese (ja)
Other versions
JP3491298B2 (en
Inventor
Makoto Kojima
誠 小島
Masayuki Satake
正之 佐竹
Tetsuo Komata
哲夫 小俣
Hozumi Tanaka
穂積 田中
Eiichiro Fukuzaki
英一郎 福崎
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 Denko Corp
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 Denko Corp filed Critical Nitto Denko Corp
Priority to JP20111493A priority Critical patent/JP3491298B2/en
Publication of JPH0734052A publication Critical patent/JPH0734052A/en
Application granted granted Critical
Publication of JP3491298B2 publication Critical patent/JP3491298B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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

Abstract

PURPOSE:To obtain the subject adhesive containing an acrylic polymer obtained by copolymerization of an acrylic monomer and a specific monomer as a main component, having good adhesiveness to various adherends, excellent in moisture proof characteristics and having high reliability. CONSTITUTION:This adhesive is obtained by copolymerizing a monomer mixture of (A) 60-97wt.% of an acrylic monomer expressed by formula I (R<1> is H or methyl; R<2> is a 2-4C alkyl), (B) 3-30wt.% of a maleimide compound expressed by formula II (R<3> is H or a monovalent organic group) and (C) 3-30wt.% of other monomer [e.g. (meth)acrylic acid or carboxyethyl acrylate] copolymerizable with the components A and B.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、アクリル系重合体を主
成分とした接着性能および耐湿特性にすぐれる感圧性接
着剤と、これをシ―ト状やテ―プ状などの形態とした接
着シ―ト類とに関するものである。
TECHNICAL FIELD The present invention relates to a pressure-sensitive adhesive containing an acrylic polymer as a main component and having excellent adhesive performance and moisture resistance, and a sheet-shaped or tape-shaped adhesive. It is related to adhesive sheets.

【0002】[0002]

【従来の技術】アクリル系重合体を主成分とした感圧性
接着剤は、上記重合体に起因して、耐光性、耐候性、耐
油性などにすぐれるという利点がある。また、プラスチ
ツクや紙などを表面基材としたアクリル系の感圧性接着
テ―プでは、接着力、凝集力などの接着性能や、耐熱
性、耐候性などの耐老化性能にすぐれていることから、
各種の分野で幅広く利用されている。
2. Description of the Related Art A pressure sensitive adhesive containing an acrylic polymer as a main component has an advantage that it is excellent in light resistance, weather resistance and oil resistance due to the above polymer. In addition, acrylic pressure-sensitive adhesive tape with plastic or paper as the surface substrate has excellent adhesive performance such as adhesive strength and cohesive strength, and aging resistance such as heat resistance and weather resistance. ,
Widely used in various fields.

【0003】最近では、作業の簡便化や作業環境の向上
を目的として、液状タイプの接着剤に代えて、シ―ト状
やテ―プ状などの形態とした感圧性接着剤を用いて接着
処理することが、定着してきており、これら処理に際
し、接着力、凝集力などの各種性能の更なる向上が望ま
れている。
Recently, for the purpose of simplifying the work and improving the working environment, a pressure-sensitive adhesive in the form of a sheet or tape is used instead of the liquid type adhesive. The treatment has become established, and further improvements in various properties such as adhesive force and cohesive force are desired in these treatments.

【0004】このような要望に対し、とくに接着力、凝
集力などの接着性能の改善には、アクリル系重合体の合
成に際し、アクリル系単量体とともに、各種の極性基含
有単量体を併用することが、よく行われている。
In order to meet such demands, in particular, in order to improve the adhesive performance such as adhesive force and cohesive force, various polar group-containing monomers are used together with the acrylic monomer during the synthesis of the acrylic polymer. It is often done.

【0005】[0005]

【発明が解決しようとする課題】しかし、極性基含有単
量体の使用は、感圧性接着剤の耐湿特性を損なう、つま
り多湿環境下で接着力が経時的に低下する弊害を生じや
すく、信頼性に劣る。このため、上記単量体の使用によ
る接着性能の改善には、限度がある。
However, the use of a polar group-containing monomer tends to impair the moisture resistance of the pressure-sensitive adhesive, that is, the adhesive strength tends to decrease with time in a humid environment, which is a problem in reliability. Inferior in sex. Therefore, there is a limit to the improvement of the adhesive performance by using the above monomer.

【0006】本発明は、上記従来の事情に鑑み、接着性
能にすぐれるとともに、耐湿特性の改善された、信頼性
の高い感圧性接着剤と、これをシ―ト状やテ―プ状など
の形態とした接着シ―ト類を提供することを目的として
いる。
In view of the above-mentioned conventional circumstances, the present invention provides a highly reliable pressure-sensitive adhesive having excellent adhesive performance and improved moisture resistance, and a sheet-like or tape-like adhesive. The purpose is to provide adhesive sheets in the form of.

【0007】[0007]

【課題を解決するための手段】本発明者らは、上記の目
的を達成するために、鋭意検討した結果、アクリル系単
量体と特定の単量体との共重合体からなるアクリル系重
合体を用いることにより、接着性能および耐湿特性にす
ぐれる信頼性の高い感圧性接着剤が得られることを知
り、本発明を完成するに至つた。
Means for Solving the Problems As a result of intensive studies to achieve the above object, the inventors of the present invention have found that an acrylic polymer composed of a copolymer of an acrylic monomer and a specific monomer is used. The inventors have found that a highly reliable pressure-sensitive adhesive having excellent adhesiveness and moisture resistance can be obtained by using the combined material, and have completed the present invention.

【0008】すなわち、本発明は、アクリル系重合体と
して、下記のa〜c成分; a)つぎの式(I); CH2 =C(R1 )COOR2 …(I) (式中、R1 は水素またはメチル基、R2 は炭素数 2〜14のアルキル基である)で表されるアクリル系単
量体50〜98重量% b)つぎの式(II); (式中、R3 は水素または1価の有機基である)で表さ
れるマレイミド化合物2〜50重量% c)上記のa,b成分と共重合可能な他の単量体0〜3
0重量%からなる単量体混合物の共重合体を主成分とす
る感圧性接着剤と、この感圧性接着剤からなる層を支持
体の片面または両面に有するシ―ト状やテ―プ状などの
形態とした接着シ―ト類とに係るものである。
That is, the present invention provides, as an acrylic polymer, the following components a to c; a) the following formula (I); CH 2 ═C (R 1 ) COOR 2 ... (I) (wherein R 1 is hydrogen or a methyl group, and R 2 is an alkyl group having 2 to 14 carbon atoms) 50 to 98% by weight of an acrylic monomer b) The following formula (II); (In the formula, R 3 is hydrogen or a monovalent organic group) 2 to 50 wt% of maleimide compound c) Other monomers 0 to 3 copolymerizable with the above-mentioned a and b components
A pressure-sensitive adhesive containing a copolymer of a monomer mixture of 0% by weight as a main component, and a sheet-like or tape-like having a layer of this pressure-sensitive adhesive on one or both sides of a support. The present invention relates to adhesive sheets in the form of the above.

【0009】[0009]

【発明の構成・作用】本発明におけるa成分としてのア
クリル系単量体は、前記の式(I)中のR2が、たとえ
ば、ブチル基、イソブチル基、イソアミル基、ヘキシル
基、ヘプチル基、2−エチルヘキシル基、イソオクチル
基、イソノニル基、イソデシル基などのアルキル基から
なるアクリル酸またはメタクリル酸のエステルである。
2 の炭素数が2未満となると、ガラス転移温度、いわ
ゆるTgの高い材料となつて、感圧性接着剤としての濡
れ性が低下し、初期接着性(タツク)が悪くなり、また
14を超えると、接着力に劣る問題がある。
In the acrylic monomer as the component a in the present invention, R 2 in the above formula (I) is, for example, butyl group, isobutyl group, isoamyl group, hexyl group, heptyl group, It is an ester of acrylic acid or methacrylic acid composed of an alkyl group such as a 2-ethylhexyl group, an isooctyl group, an isononyl group, and an isodecyl group.
When the carbon number of R 2 is less than 2, it becomes a material having a high glass transition temperature, so-called Tg, and the wettability as a pressure-sensitive adhesive decreases, the initial adhesiveness (tack) deteriorates, and it exceeds 14 Then, there is a problem of poor adhesion.

【0010】このa成分のアクリル系単量体は、単量体
全体量の50〜98重量%、好ましくは60〜97重量
%の範囲で、その1種または2種以上が用いられる。5
0重量%未満となると、前記したアルキル基の炭素数が
2未満である場合と同様に、Tgの低い成分が少なくな
りすぎて感圧性接着剤としての性能を発揮できず、また
98重量%を超えると、そのぶん後述するb成分の絶対
量が不足し、接着性能および耐湿特性を両立させること
が難しくなる。
The acrylic monomer as the component a is used in the range of 50 to 98% by weight, preferably 60 to 97% by weight, based on the total amount of the monomers, and one or more of them are used. 5
When it is less than 0% by weight, as in the case where the number of carbon atoms of the alkyl group is less than 2, the component having a low Tg becomes too small to exhibit the performance as a pressure-sensitive adhesive, and the amount of 98% by weight is reduced. If it exceeds, the absolute amount of the component b, which will be described later, is insufficient, and it becomes difficult to achieve both adhesive performance and moisture resistance.

【0011】本発明におけるb成分としてのマレイミド
化合物は、前記の式(II)中のR3が、水素(マレイミ
ドそのもの)であるか、あるいはアルキル基、シクロア
ルキル基、アリル基、アラルキル基またはこれらの基に
さらに官能基が導入された1価の有機基、たとえば、メ
チル基、エチル基、プロピル基、ブチル基、ヘキシル
基、オクチル基、ラウリル基、シクロヘキシル基、フエ
ニル基、メチルフエニル基、メトキシフエニル基、クロ
ロフエニル基、ニトロフエニル基、カルボキシフエニル
基などが挙げられる。
In the maleimide compound as the component b in the present invention, R 3 in the above formula (II) is hydrogen (maleimide itself), or an alkyl group, a cycloalkyl group, an allyl group, an aralkyl group or these A monovalent organic group in which a functional group is further introduced into, for example, methyl group, ethyl group, propyl group, butyl group, hexyl group, octyl group, lauryl group, cyclohexyl group, phenyl group, methylphenyl group, methoxyphenyl group. Examples thereof include an enyl group, a chlorophenyl group, a nitrophenyl group and a carboxyphenyl group.

【0012】このb成分のマレイミド化合物は、単量体
全体量の2〜50重量%、好ましくは3〜30重量%の
範囲で、その1種または2種以上が用いられる。2重量
%未満となると、本発明の目的とする耐湿特性の改善効
果が得られず、また50重量%を超えると、感圧性接着
剤として望まれる低いTgに保ちにくくなり、初期接着
力が不足することになる。
The maleimide compound as the component b is used in the range of 2 to 50% by weight, preferably 3 to 30% by weight, based on the total amount of the monomers, and one or more types thereof are used. If it is less than 2% by weight, the desired effect of improving the moisture resistance of the present invention cannot be obtained, and if it exceeds 50% by weight, it is difficult to maintain the low Tg desired as a pressure-sensitive adhesive, and the initial adhesive strength is insufficient. Will be done.

【0013】本発明におけるc成分の単量体は、上記の
a,b成分と共重合可能な単量体であればよく、たとえ
ば、(メタ)アクリル酸、カルボキシエチルアクリレ―
ト、イタコン酸、マレイン酸、クロトン酸などのカルボ
キシル基含有単量体;2−ヒドロキシエチル(メタ)ア
クリロイルホスフエイトなどのリン酸基含有単量体;
(メタ)アクリルアミド、N−置換(メタ)アクリルア
ミドなどのアミド系単量体;酢酸ビニル、N−ビニルピ
ロリドン、N−ビニルカルボン酸アミド類、スチレンな
どのビニル系単量体などが挙げられる。
The monomer of the component c in the present invention may be any monomer which can be copolymerized with the above-mentioned components a and b, and examples thereof include (meth) acrylic acid and carboxyethyl acrylate.
Carboxyl group-containing monomers such as glutamine, itaconic acid, maleic acid, and crotonic acid; Phosphoric acid group-containing monomers such as 2-hydroxyethyl (meth) acryloyl phosphate;
Amide-based monomers such as (meth) acrylamide and N-substituted (meth) acrylamide; vinyl-based monomers such as vinyl acetate, N-vinylpyrrolidone, N-vinylcarboxylic acid amides, and styrene.

【0014】また、(メタ)アクリル酸グリシジル、
(メタ)アクリル酸2−ヒドロキシエチル、(メタ)ア
クリル酸2−ヒドロキシプロピル、(メタ)アクリル酸
メチル、テトラヒドロフルフリル(メタ)アクリレ―
ト、ポリエチレングリコ―ル(メタ)アクリレ―ト、ポ
リプロピレングリコ―ル(メタ)アクリレ―ト、フツ素
(メタ)アクリレ―ト、シリコン(メタ)アクリレ―ト
などのa成分以外の(メタ)アクリル酸エステル系単量
体なども使用できる。
Further, glycidyl (meth) acrylate,
2-Hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, methyl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate
(Meth) acryl other than a-component such as polyethylene glycol (meth) acrylate, polypropylene glycol (meth) acrylate, fluorine (meth) acrylate, silicone (meth) acrylate, etc. Acid ester type monomers and the like can also be used.

【0015】さらに、多官能(メタ)アクリレ―トなど
も、電子線などによる無架橋剤下での後架橋を行いたい
場合などに、必要により使用できる。具体的には、ヘキ
サンジオ―ルジ(メタ)アクリレ―ト、(ポリ)エチレ
ングリコ―ルジ(メタ)アクリレ―ト、(ポリ)プロピ
レングリコ―ルジ(メタ)アクリレ―ト、ネオペンチル
グリコ―ルジ(メタ)アクリレ―ト、ペンタエリスリト
―ルジ(メタ)アクリレ―ト、トリメチロ―ルプロパン
トリ(メタ)アクリレ―ト、ペンタエリスリト―ルトリ
(メタ)アクリレ―ト、ジペンタエリスリト―ルヘキサ
(メタ)アクリレ―ト、その他エポキシ(メタ)アクリ
レ―ト、ポリエステル(メタ)アクリレ―ト、ウレタン
(メタ)アクリレ―トなどが挙げられる。
Further, a polyfunctional (meth) acrylate or the like can also be used, if necessary, when post-crosslinking with an electron beam or the like under a non-crosslinking agent is desired. Specifically, hexanediol di (meth) acrylate, (poly) ethylene glycol di (meth) acrylate, (poly) propylene glycol di (meth) acrylate, neopentyl glycol di (meth) ) Acrylate, pentaerythritol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol hexa (meth) acrylate And other epoxy (meth) acrylates, polyester (meth) acrylates, urethane (meth) acrylates and the like.

【0016】このc成分の単量体は、必要により単量体
全体量の30重量%以下、好ましくは25重量%以下の
範囲で、その1種または2種以上が用いられる。30重
量%を超えると、アクリル系としての性能を発現しにく
くなつたり、感圧性接着剤としての特性のバランスがと
れなくなる。
If necessary, one or more monomers of the component c may be used in an amount of 30% by weight or less, preferably 25% by weight or less, based on the total amount of the monomers. If it exceeds 30% by weight, the performance as an acrylic resin is difficult to be expressed, and the properties as a pressure-sensitive adhesive cannot be balanced.

【0017】本発明のアクリル系重合体は、上記のa,
b二成分またはa〜c三成分からなる単量体混合物の共
重合体であつて、この共重合体は、上記の単量体混合物
を、常法により、溶液重合法、乳化重合法、塊状重合
法、けんだく重合法などの方法で共重合させることによ
り、得ることができる。上記重合法の中でも、塊状重合
法では、紫外線照射による重合方式が好ましく採用され
る。
The acrylic polymer of the present invention has the above-mentioned a,
A copolymer of a monomer mixture consisting of two components b or three components a to c, which is obtained by subjecting the above-mentioned monomer mixture to a solution polymerization method, an emulsion polymerization method, or a block method by a conventional method. It can be obtained by copolymerization by a method such as a polymerization method or a kendaku polymerization method. Among the above-mentioned polymerization methods, in the bulk polymerization method, a polymerization method by ultraviolet irradiation is preferably adopted.

【0018】上記の共重合に際して、熱重合開始剤また
は光重合開始剤を、必要により重合原料(固形分)全体
の0.001〜5重量%の範囲で使用できる。熱重合開
始剤としては、過酸化ベンゾイル、アゾビスイソブチロ
ニトリル、tert−ブチルパ―ベンゾエ―ト、クメン
ヒドロパ―オキサイド、ジイソプロピルパ―オキシジカ
―ボネ―ト、ジ−n−プロピルパ―オキシジカ―ボネ―
ト、ジ(2−エトキシエチル)パ―オキシジカ―ボネ―
ト、tert−ブチルパ―オキシネオデカノエ―ト、t
ert−ブチルパ―オキシピバレ―ト、ジ(3,5,5
−トリメチルヘキサノイル)パ―オキサイド、ジラウロ
イルパ―オキサイド、ジプロピオニルパ―オキサイド、
ジアセチルパ―オキサイドなどが挙げられる。
In the above copolymerization, a thermal polymerization initiator or a photopolymerization initiator can be used, if necessary, in the range of 0.001 to 5% by weight based on the whole polymerization raw material (solid content). Examples of the thermal polymerization initiator include benzoyl peroxide, azobisisobutyronitrile, tert-butyl perbenzoate, cumene hydroperoxide, diisopropyl peroxy dicarbonate, di-n-propyl peroxy dicarbonate.
G, di (2-ethoxyethyl) peroxydicarbone
Tert-butyl peroxyneodecanoate, t
ert-butyl peroxypivalate, di (3,5,5
-Trimethylhexanoyl) peroxide, dilauroylperoxide, dipropionylperoxide,
Examples thereof include diacetyl peroxide.

【0019】光重合開始剤としては、4−(2−ヒドロ
キシエトキシ)フエニル(2−ヒドロキシ−2−プロピ
ル)ケトン、α−ヒドロキシ−α,α´−ジメチルアセ
トフエノン、メトキシアセトフエノン、2,2−ジメト
キシ−2−フエニルアセトフエノンなどのアセトフエノ
ン系開始剤;ベンゾインエチルエ―テル、ベンゾインイ
ソプロピルエ―テルなどのベンゾインエ―テル系開始
剤;ベンジルジメチルケタ―ルなどのケタ―ル系開始
剤;その他ハロゲン化ケトン、アシルホスフイノキシ
ド、アシルホスフオナ―トなどが挙げられる。マレイミ
ド化合物は紫外領域の比較的長波長側にまで吸収を有す
るため、上記の開始剤の中でも、とくに長波長側で活性
化する開始剤を用いるのが望ましい。
As the photopolymerization initiator, 4- (2-hydroxyethoxy) phenyl (2-hydroxy-2-propyl) ketone, α-hydroxy-α, α'-dimethylacetophenone, methoxyacetophenone, 2 , 2-Dimethoxy-2-phenylacetophenone and other acetophenone type initiators; benzoin ethyl ether, benzoin isopropyl ether and other benzoin ether type initiators; benzyl dimethyl ketal and other ketal type initiators Initiators: Other examples include halogenated ketones, acyl phosphinoxides, acyl phosphonates and the like. Since the maleimide compound has absorption up to a relatively long wavelength side in the ultraviolet region, it is preferable to use an initiator which is activated particularly on the long wavelength side among the above initiators.

【0020】本発明の感圧性接着剤は、このようにして
得られるアクリル系重合体を主成分とし、必要により天
然または合成の樹脂類、ガラス繊維、ガラスビ―ズ、金
属粉、無機粉末などの充てん剤、顔料、着色剤などの添
加剤を、任意成分として含ませることができる。
The pressure-sensitive adhesive of the present invention contains the acrylic polymer thus obtained as a main component, and if necessary, natural or synthetic resins, glass fibers, glass beads, metal powder, inorganic powder, etc. Additives such as fillers, pigments and colorants can be included as optional components.

【0021】また、この感圧性接着剤は、適宜架橋処理
を施したものであつてもよい。架橋処理は、アクリル系
重合体を得る際に、内部架橋剤として前記のような多官
能(メタ)アクリレ―トなどを添加するか、あるいはア
クリル系重合体を得たのち、外部架橋剤として多官能の
イソシアネ―ト化合物やエポキシ化合物などを添加する
ことにより、実施できる。その他、電子線照射などの活
性光線による架橋処理を施すようにしてもよい。
Further, the pressure-sensitive adhesive may be one which has been appropriately crosslinked. The cross-linking treatment is carried out by adding the above-mentioned polyfunctional (meth) acrylate as an internal cross-linking agent at the time of obtaining an acrylic polymer, or after obtaining an acrylic polymer, it is added as an external cross-linking agent. It can be carried out by adding a functional isocyanate compound or an epoxy compound. In addition, you may make it perform a bridge | crosslinking process by active rays, such as electron beam irradiation.

【0022】本発明の接着シ―ト類は、このような感圧
性接着剤からなる層を、支持体の片面または両面に所望
厚さに設けることにより、シ―ト状やテ―プ状などの形
態としたものである。上記の支持体としては、プラスチ
ツクフイルム、紙、不織布、発泡体、金属箔などを用い
ることができ、その片面または両面に剥離処理または接
着処理を施したものを使用してもよい。
The adhesive sheet of the present invention is provided with a layer made of such a pressure-sensitive adhesive on one side or both sides of the support so as to have a desired thickness. It is in the form of. As the above-mentioned support, plastic film, paper, non-woven fabric, foam, metal foil and the like can be used, and one having one surface or both surfaces subjected to a peeling treatment or an adhesive treatment may be used.

【0023】このように構成される本発明の感圧性接着
剤とその接着シ―ト類は、接着性能および耐湿特性にす
ぐれて、信頼性の高い接着処理を実現する。この理由
は、必ずしも明らかではないが、アクリル系重合体を構
成する前記b成分としてのマレイミド化合物が耐水性に
すぐれて、かつ適度な極性を有し、これが感圧性接着剤
に適度な凝集力をもたらすことなどによるものと推定さ
れる。
The pressure-sensitive adhesive of the present invention and the adhesive sheets thereof having the above-described structure realize a highly reliable adhesive treatment with excellent adhesive performance and moisture resistance. The reason for this is not clear, but the maleimide compound as the component b constituting the acrylic polymer is excellent in water resistance and has an appropriate polarity, which gives the pressure-sensitive adhesive an appropriate cohesive force. It is presumed that this is due to things such as bringing.

【0024】[0024]

【発明の効果】以上のように、本発明では、アクリル系
単量体と特定の単量体との共重合体からなるアクリル系
重合体を主成分としたことにより、様々な被着体に対し
て良好な接着性を示すとともに、耐湿特性にもすぐれ
る、信頼性の高い感圧性接着剤とその接着シ―ト類を提
供することができる。
As described above, according to the present invention, since the main component is the acrylic polymer which is a copolymer of the acrylic monomer and the specific monomer, various adherends can be obtained. On the other hand, it is possible to provide a highly reliable pressure-sensitive adhesive which exhibits excellent adhesiveness and also has excellent moisture resistance, and its adhesive sheet.

【0025】[0025]

【実施例】つぎに、本発明の実施例を記載して、より具
体的に説明する。なお、以下において、部とあるのは重
量部を意味する。
EXAMPLES Next, examples of the present invention will be described to more specifically describe. In the following, "parts" means "parts by weight".

【0026】実施例1 冷却管、窒素導入管、温度計および撹拌装置を備えた反
応容器内に、酢酸エチル150部、アクリル酸2−エチ
ルヘキシル80部、アクリル酸5部、シクロヘキシルマ
レイミド10部、重合開始剤としてアゾビスイソブチロ
ニトリル0.5部を入れ、60℃で4時間、続いて80
℃で2時間重合して、重合率99重量%の共重合体溶液
を得た。
Example 1 150 parts of ethyl acetate, 80 parts of 2-ethylhexyl acrylate, 5 parts of acrylic acid, 10 parts of cyclohexylmaleimide, polymerization were placed in a reaction vessel equipped with a cooling tube, a nitrogen introducing tube, a thermometer and a stirrer. 0.5 parts of azobisisobutyronitrile was added as an initiator, and the mixture was heated at 60 ° C. for 4 hours and then 80
Polymerization was carried out at 0 ° C. for 2 hours to obtain a copolymer solution having a polymerization rate of 99% by weight.

【0027】この溶液に、共重合体100部に対して、
架橋剤としてトリメチロ―ルプロパン−トリレンジイソ
シアネ―ト付加物3部を加えて、感圧性接着剤溶液を調
製した。この溶液を、厚さが25μmのポリエステルフ
イルム上に塗布し、乾燥して、厚さが50μmの感圧性
接着剤の層を有する接着シ―トを作製した。
To this solution, with respect to 100 parts of the copolymer,
A pressure sensitive adhesive solution was prepared by adding 3 parts of a trimethylolpropane-tolylene diisocyanate adduct as a crosslinking agent. This solution was coated on a polyester film having a thickness of 25 μm and dried to prepare an adhesive sheet having a layer of pressure-sensitive adhesive having a thickness of 50 μm.

【0028】実施例2〜7 単量体混合物の組成を、表1および表2の如く変更した
以外は、実施例1と同様にして、重合率が98.5〜9
9%の6種の共重合体溶液を得、これに実施例1と同じ
架橋剤を実施例1と同量加えて、6種の感圧性接着剤溶
液を調製した。各溶液を用いて、実施例1と同様にし
て、6種の接着シ―トを作製した。
Examples 2 to 7 The polymerization rate was 98.5 to 9 in the same manner as in Example 1 except that the composition of the monomer mixture was changed as shown in Tables 1 and 2.
6% copolymer solution of 9% was obtained, and the same cross-linking agent as in Example 1 was added thereto in the same amount as in Example 1 to prepare 6 pressure-sensitive adhesive solutions. Six kinds of adhesive sheets were produced in the same manner as in Example 1 using each solution.

【0029】比較例1〜3 単量体混合物の組成を、表3の如く変更した以外は、実
施例1と同様にして、重合率が99%の3種の共重合体
溶液を得、これに実施例1と同じ架橋剤を実施例1と同
量加えて、3種の感圧性接着剤溶液を調製した。各溶液
を用いて、実施例1と同様にして、3種の接着シ―トを
作製した。
Comparative Examples 1 to 3 In the same manner as in Example 1 except that the composition of the monomer mixture was changed as shown in Table 3, three types of copolymer solutions having a polymerization rate of 99% were obtained. The same cross-linking agent as in Example 1 was added thereto to prepare 3 kinds of pressure-sensitive adhesive solutions. Using each solution, three kinds of adhesive sheets were produced in the same manner as in Example 1.

【0030】[0030]

【表1】 [Table 1]

【0031】[0031]

【表2】 [Table 2]

【0032】[0032]

【表3】 [Table 3]

【0033】上記の実施例1〜7および比較例1〜3で
作製した接着シ―トにつき、感圧性接着剤としての接着
性能(とくにタツク)の良否を調べるとともに、下記の
要領で耐湿特性試験を行つた。これらの結果を、後記の
表4に示す。
With respect to the adhesive sheets prepared in Examples 1 to 7 and Comparative Examples 1 to 3 above, the quality of the adhesive performance (particularly tack) as a pressure-sensitive adhesive was examined, and a moisture resistance test was conducted in the following manner. I went. The results are shown in Table 4 below.

【0034】<耐湿特性試験>#280のサンドペ―パ
で表面を研磨し、溶剤で脱脂した清浄なSUS板に、接
着シ―トを20mm幅で貼布し、50℃で5日間加温、エ
―ジングし、接着力が安定したときの接着力(初期の接
着力)と、これを蒸留水に4日間浸漬したのちの接着力
(試験後の接着力)とを、引張速度300mm/分にて1
80度剥離で、測定した。また、(試験後の接着力/初
期の接着力)×100%として、試験後の接着力の保持
率を算出した。
<Moisture resistance test> A clean SUS plate, the surface of which was sanded with # 280 sandpaper and degreased with a solvent, was pasted with an adhesive sheet in a width of 20 mm and heated at 50 ° C. for 5 days. The adhesive force when the adhesive force is aged and the adhesive force is stable (initial adhesive force) and the adhesive force after immersing this in distilled water for 4 days (adhesive force after the test) are drawn at a pulling speed of 300 mm / min. At 1
It was measured by peeling at 80 degrees. In addition, the retention rate of the adhesive force after the test was calculated as (adhesive force after the test / initial adhesive force) × 100%.

【0035】[0035]

【表4】 [Table 4]

【0036】上記の表4の結果から、本発明の実施例1
〜7の接着シ―トは、比較例1〜3の接着シ―トに比べ
て、良好な接着性能を有するとともに、耐湿特性に格段
にすぐれており、信頼性の非常に高いものであることが
わかる。
From the results of Table 4 above, Example 1 of the present invention
The adhesive sheets of Nos. 7 to 7 have excellent adhesive performance as compared with the adhesive sheets of Comparative Examples 1 to 3 and have extremely excellent moisture resistance characteristics, and have extremely high reliability. I understand.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 田中 穂積 大阪府茨木市下穂積1丁目1番2号 日東 電工株式会社内 (72)発明者 福崎 英一郎 大阪府茨木市下穂積1丁目1番2号 日東 電工株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hozumi Tanaka 1-2-2 Shimohozumi, Ibaraki-shi, Osaka Nitto Denko Corporation (72) Inventor Eiichiro Fukusaki 1-2-1, Shimohozumi, Ibaraki-shi, Osaka Nitto Denko Corporation

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 下記のa〜c成分; a)つぎの式(I); CH2 =C(R1 )COOR2 …(I) (式中、R1 は水素またはメチル基、R2 は炭素数 2〜14のアルキル基である)で表されるアクリル系単
量体50〜98重量% b)つぎの式(II); (式中、R3 は水素または1価の有機基である)で表さ
れるマレイミド化合物2〜50重量% c)上記のa,b成分と共重合可能な他の単量体0〜3
0重量%からなる単量体混合物の共重合体を主成分とす
る感圧性接着剤。
1. The following components a to c; a) the following formula (I); CH 2 ═C (R 1 ) COOR 2 (I) (wherein R 1 is hydrogen or a methyl group, and R 2 is 50 to 98% by weight of an acrylic monomer represented by an alkyl group having 2 to 14 carbon atoms) b) the following formula (II); (In the formula, R 3 is hydrogen or a monovalent organic group) 2 to 50 wt% of maleimide compound c) Other monomers 0 to 3 copolymerizable with the above-mentioned a and b components
A pressure-sensitive adhesive whose main component is a copolymer of 0% by weight of a monomer mixture.
【請求項2】 支持体の片面または両面に請求項1に記
載の感圧性接着剤からなる層を有する接着シ―ト類。
2. Adhesive sheets having a layer comprising the pressure-sensitive adhesive according to claim 1 on one side or both sides of a support.
JP20111493A 1993-07-20 1993-07-20 Pressure-sensitive adhesives and their adhesive sheets Expired - Lifetime JP3491298B2 (en)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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JP2001354931A (en) * 2000-06-12 2001-12-25 Nitto Denko Corp Acrylic adhesive and adhesive sheet, or the like
CN1109086C (en) * 2000-07-19 2003-05-21 湖北省化学研究所 Reaction-type flame-retarding adhesive for flexible PCB and its preparing process
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Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001354931A (en) * 2000-06-12 2001-12-25 Nitto Denko Corp Acrylic adhesive and adhesive sheet, or the like
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JP2009203450A (en) * 2008-01-30 2009-09-10 Tokyo Ohka Kogyo Co Ltd Adhesive composition and adhesive film
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US8901234B2 (en) 2008-06-17 2014-12-02 Tokyo Ohka Kogyo Co., Ltd. Adhesive composition
US8901235B2 (en) 2008-06-17 2014-12-02 Tokyo Ohka Kogyo Co., Ltd. Adhesive composition, film adhesive, and heat treatment method
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US11795351B2 (en) 2018-02-20 2023-10-24 Lg Chem, Ltd. Adhesive composition and adhesive film comprising same

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