JPH07138544A - Pressure-sensitive acrylic adhesive composition - Google Patents

Pressure-sensitive acrylic adhesive composition

Info

Publication number
JPH07138544A
JPH07138544A JP28902393A JP28902393A JPH07138544A JP H07138544 A JPH07138544 A JP H07138544A JP 28902393 A JP28902393 A JP 28902393A JP 28902393 A JP28902393 A JP 28902393A JP H07138544 A JPH07138544 A JP H07138544A
Authority
JP
Japan
Prior art keywords
sensitive adhesive
pressure
acrylic
adhesive composition
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP28902393A
Other languages
Japanese (ja)
Inventor
Masateru Fukuoka
正輝 福岡
Hidekazu Sawada
英一 澤田
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP28902393A priority Critical patent/JPH07138544A/en
Publication of JPH07138544A publication Critical patent/JPH07138544A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To obtain the title compsn. which has a stable cross-linkability and exhibits excellent adhesive properties, esp. resistance to peeling, in bonding low-polar adherends. CONSTITUTION:The title compsn. contains 100 pts.wt. acrylic copoymler obtd. by copolymerizing 99.5-90wt.% 2-18C alkyl (meth)acrylate with 0.5-10wt.% polymerizable unsatd. carboxylic acid, 5-40 pts.wt. pentaerythritol ester of polymerized rosin, and 0.01-5 pts.wt. aziridine compd. having at least two aziridine rinds.

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、例えば粘着ラベル、粘
着テープ、粘着シート等の粘着加工製品に好適に使用さ
れるアクリル系感圧性接着剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an acrylic pressure-sensitive adhesive composition suitable for use in adhesive processed products such as adhesive labels, adhesive tapes and adhesive sheets.

【0002】[0002]

【従来の技術】従来、粘着ラベル、粘着テープ、粘着シ
ート等の粘着製品用感圧性接着剤としては、アクリル系
共重合体を主成分とするアクリル系感圧性接着剤や天然
ゴム、合成ゴムなどを主成分とするゴム系感圧性接着剤
等が使用されている。
2. Description of the Related Art Conventionally, pressure-sensitive adhesives for pressure-sensitive adhesive products such as pressure-sensitive adhesive labels, pressure-sensitive adhesive tapes, pressure-sensitive adhesive sheets, etc. have mainly been acrylic pressure-sensitive adhesives containing acrylic copolymers, natural rubber, synthetic rubber, etc. A rubber-based pressure-sensitive adhesive containing as a main component is used.

【0003】前者のアクリル系感圧性接着剤は、アクリ
ル系共重合体のモノマー成分を選択することによって粘
着性能を容易に調整できる利点を有しており多用されて
いる。
The former acrylic pressure-sensitive adhesive is widely used because it has the advantage that the adhesive performance can be easily adjusted by selecting the monomer component of the acrylic copolymer.

【0004】ところが、通常のアクリル系感圧性接着剤
は、ポリエチレンやポリプロピレン等の低極性表面を有
する被着体に対する接着力は充分とは言えず、これに対
処する為、アクリル系感圧性接着剤に粘着付与樹脂を配
合する方法が一般的に行われている。
However, ordinary acrylic pressure-sensitive adhesives do not have sufficient adhesive force to adherends having a low polarity surface such as polyethylene and polypropylene, and in order to deal with this, acrylic pressure-sensitive adhesives are used. A method of blending a tackifying resin with is generally used.

【0005】この様なアクリル系感圧性接着剤の一例と
して、アクリル系共重合体100重量部に対して、粘着
付与樹脂として重合ロジンのペンタエリスリトールエス
テルを2〜50重量部と架橋剤としてイソシアネート化
合物を0.2〜3重量部含有させる方法が提案されてい
る(特公平5−60511号公報)が、この方法の場
合、イソシアネート化合物を架橋剤としているので、環
境条件例えば湿度の影響を受けて架橋に長時間を要した
り、架橋度そのものが均一性を欠き、その結果得られる
感圧性接着剤の接着特性、例えば加温時の保持力や耐ク
リープ性等が充分でなかったりばらつくと言う問題点が
ある。
As an example of such an acrylic pressure-sensitive adhesive, 100 parts by weight of an acrylic copolymer, 2 to 50 parts by weight of pentaerythritol ester of polymerized rosin as a tackifying resin, and an isocyanate compound as a crosslinking agent are used. Is proposed (Japanese Patent Publication No. 5-60511), but in the case of this method, since an isocyanate compound is used as a crosslinking agent, it is affected by environmental conditions such as humidity. It is said that it takes a long time to crosslink, or the degree of crosslink itself lacks uniformity, and as a result, the adhesive properties of the pressure sensitive adhesive, such as holding power during heating and creep resistance, are insufficient or vary. There is a problem.

【0006】[0006]

【発明が解決しようとする課題】本発明は、上記従来の
問題点を解決するため、環境条件に影響されない安定的
な架橋性と短時間に架橋反応が終結するという生産性を
有し、各種被着体に対して優れた接着特性、特に加温時
の保持力や耐クリープ性を発現すると共に、低極性被着
体に対する接着諸特性、特に耐剥離性に優れるアクリル
系感圧性接着剤組成物を提供することを目的とする。
In order to solve the above-mentioned conventional problems, the present invention has stable crosslinkability that is not affected by environmental conditions and productivity that the crosslinking reaction is terminated in a short time, and Acrylic pressure-sensitive adhesive composition that exhibits excellent adhesive properties to adherends, especially holding power and creep resistance when heated, and excellent adhesive properties to low-polar adherends, especially excellent peel resistance. The purpose is to provide things.

【0007】[0007]

【課題を解決するための手段】本発明のアクリル系感圧
性接着剤組成物は、アルキル基の炭素数が2〜18の
(メタ)アクリル酸アルキルエステル99.5〜90重
量%と重合性不飽和カルボン酸0.5〜10重量%とを
共重合して得られるアクリル系共重合体の固形分100
重量部に対し、重合ロジンのペンタエリスリトールエス
テル5〜40重量部及び1分子中に2個以上のアジリジ
ン環を有するアジリジン系化合物0.01〜0.5重量
部が含有されていることを特徴とし、そのことにより上
記目的が達成される。尚、本発明において、(メタ)ア
クリルとはアクリル又はメタクリルを表すものとする。
The acrylic pressure-sensitive adhesive composition of the present invention comprises 99.5 to 90% by weight of a (meth) acrylic acid alkyl ester having an alkyl group having 2 to 18 carbon atoms and a polymerizable non-polymerizable adhesive. Solid content 100 of acrylic copolymer obtained by copolymerizing with 0.5 to 10% by weight of saturated carboxylic acid
5 to 40 parts by weight of pentaerythritol ester of polymerized rosin and 0.01 to 0.5 parts by weight of an aziridine compound having two or more aziridine rings in one molecule are contained per part by weight. Therefore, the above object is achieved. In addition, in this invention, (meth) acryl shall mean acryl or methacryl.

【0008】本発明のアクリル系感圧性接着剤組成物を
構成するアクリル系共重合体の重合に使用されるアルキ
ル基の炭素数が2〜18の(メタ)アクリル酸アルキル
エステルとしては、(メタ)アクリル酸エチルエステ
ル、(メタ)アクリル酸n−プロピルエステル、(メ
タ)アクリル酸iso−プロピルエステル、(メタ)ア
クリル酸n−ブチルエステル、(メタ)アクリル酸n−
オクチルエステル、(メタ)アクリル酸2−エチルヘキ
シルエステル、(メタ)アクリル酸ノニルエステル、
(メタ)アクリル酸ドデシルエステル等が挙げられ、な
かでもアクリル酸エチルエステル、アクリル酸n−ブチ
ルエステル、アクリル酸2−エチルヘキシルエステル等
が好適に使用される。アルキル基の炭素数が2〜18の
範囲外であると、得られる感圧性接着剤組成物の粘着性
能が損なわれるので好ましくない。
The (meth) acrylic acid alkyl ester having 2 to 18 carbon atoms in the alkyl group used for the polymerization of the acrylic copolymer constituting the acrylic pressure-sensitive adhesive composition of the present invention includes (meth ) Acrylic acid ethyl ester, (meth) acrylic acid n-propyl ester, (meth) acrylic acid iso-propyl ester, (meth) acrylic acid n-butyl ester, (meth) acrylic acid n-
Octyl ester, (meth) acrylic acid 2-ethylhexyl ester, (meth) acrylic acid nonyl ester,
Examples thereof include (meth) acrylic acid dodecyl ester, and among them, acrylic acid ethyl ester, acrylic acid n-butyl ester, acrylic acid 2-ethylhexyl ester and the like are preferably used. When the number of carbon atoms of the alkyl group is outside the range of 2 to 18, the pressure-sensitive adhesive composition obtained is impaired in tackiness, which is not preferable.

【0009】上記アクリル系共重合体に共重合成分とし
て使用される重合性不飽和カルボン酸としては、(メ
タ)アクリル酸、イタコン酸等が挙げられる。
Examples of the polymerizable unsaturated carboxylic acid used as a copolymerization component in the acrylic copolymer include (meth) acrylic acid and itaconic acid.

【0010】本発明においては、上記重合性不飽和カル
ボン酸の共重合比率は0.5〜10重量%の範囲にある
ことが必要であり、特に1〜5重量%が好ましい。重合
性不飽和カルボン酸の共重合比率が0.5重量%未満で
あると得られるアクリル系感圧性接着剤組成物の架橋度
が上昇しないので充分な保持力や耐クリープ性が発現さ
れず、逆に10重量%を超えると得られるアクリル系感
圧性接着剤組成物の初期接着力が低下する。
In the present invention, the copolymerization ratio of the above polymerizable unsaturated carboxylic acid needs to be in the range of 0.5 to 10% by weight, preferably 1 to 5% by weight. When the copolymerization ratio of the polymerizable unsaturated carboxylic acid is less than 0.5% by weight, the degree of crosslinking of the acrylic pressure-sensitive adhesive composition obtained does not increase, so that sufficient holding power and creep resistance are not expressed. On the contrary, when it exceeds 10% by weight, the initial adhesive strength of the obtained acrylic pressure-sensitive adhesive composition is lowered.

【0011】本発明のアクリル系感圧性接着剤組成物に
は、粘着付与樹脂として重合ロジンのペンタエリスリト
ールエステルが含有されていることが必要である。
The acrylic pressure-sensitive adhesive composition of the present invention must contain a pentaerythritol ester of polymerized rosin as a tackifying resin.

【0012】上記重合ロジンのペンタエリスリトールエ
ステルは、ロジンを重合して融点を高めた重合ロジンを
ペンタエリスリトールでエステル化して得られるカルボ
キシル基を含む粘着付与樹脂であり、具体的市販品とし
ては、商品名「ペンセルD125」、「ペンセルD13
5」、「ペンセルD160」(以上、荒川化学工業社
製)、「ペンタリンC」(理化ハーキュレス社製)等が
挙げられる。
The above-mentioned pentaerythritol ester of polymerized rosin is a tackifying resin containing a carboxyl group obtained by esterifying polymerized rosin obtained by polymerizing rosin to raise the melting point with pentaerythritol. Specific commercial products include commercial products. Name "Pencel D125", "Pencel D13
5 ”,“ Pencel D160 ”(above, manufactured by Arakawa Chemical Industry Co., Ltd.),“ Pentaline C ”(manufactured by Rika Hercules Co., Ltd.) and the like.

【0013】本発明においては、上記重合ロジンのペン
タエリスリトールエステルの含有量は、前記アクリル系
共重合体の固形分100重量部に対し5〜40重量部の
範囲にあることが必要である。アクリル系共重合体の固
形分100重量部に対する重合ロジンのペンタエリスリ
トールエステルの含有量が5重量部未満であると粘着付
与樹脂添加の効果が得られず、逆に40重量部を超える
と得られるアクリル系感圧性接着剤組成物の初期接着力
や耐熱性が低下する。
In the present invention, the content of the pentaerythritol ester of the polymerized rosin needs to be in the range of 5 to 40 parts by weight with respect to 100 parts by weight of the solid content of the acrylic copolymer. If the content of the pentaerythritol ester of the polymerized rosin is less than 5 parts by weight based on 100 parts by weight of the solid content of the acrylic copolymer, the effect of adding the tackifying resin cannot be obtained, and if it exceeds 40 parts by weight, it is obtained. The initial adhesive strength and heat resistance of the acrylic pressure-sensitive adhesive composition are reduced.

【0014】本発明のアクリル系感圧性接着剤組成物に
は、架橋剤として1分子中に2個以上のアジリジン環を
有するアジリジン系化合物が含有されていることが必要
である。
The acrylic pressure-sensitive adhesive composition of the present invention needs to contain an aziridine compound having two or more aziridine rings in one molecule as a crosslinking agent.

【0015】一般に、アクリル系感圧性接着剤の架橋剤
としてはイソシアネート系化合物が多用される。しか
し、イソシアネート系化合物はアクリル系重合体中の水
酸基やカルボキシル基と非選択的に反応するが、これら
の反応は前述の如く環境条件例えば湿度の影響を受けや
すいので架橋に長時間を要したり、得られる感圧性接着
剤の接着特性のばらつきが大きくなったりする欠点があ
る。これに対し、本発明で用いる1分子中に2個以上の
アジリジン環を有するアジリジン系化合物は、アクリル
系共重合体中のカルボキシル基と選択的且つ速やかに反
応するので湿度のような環境条件の影響を受けにくく、
架橋が短時間で安定的に進行すると共に、得られる感圧
性接着剤組成物の接着特性も安定化する利点がある。
Generally, an isocyanate compound is often used as a cross-linking agent for acrylic pressure-sensitive adhesives. However, an isocyanate compound non-selectively reacts with a hydroxyl group or a carboxyl group in an acrylic polymer, but since these reactions are easily affected by environmental conditions such as humidity, it takes a long time to crosslink. However, there is a drawback that the obtained pressure-sensitive adhesive has a large variation in adhesive properties. On the other hand, the aziridine-based compound having two or more aziridine rings in one molecule used in the present invention selectively and rapidly reacts with the carboxyl group in the acrylic copolymer, so that it can be used under environmental conditions such as humidity. Less affected,
There are advantages that the crosslinking proceeds stably in a short time and the adhesive properties of the obtained pressure-sensitive adhesive composition are also stabilized.

【0016】上記アジリジン系化合物とは1分子中にア
ジリジン環を2個以上有する化合物であり、具体的に
は、N,N’−ジフェニルメタン−4,4’−ビス(1
−アジリジンカルボキシアミド)、トリメチロールプロ
パン−トリス−β−アジリジニルプロピオネート、N,
N’−ヘキサメチレン−1,6−ビス(1−アジリジン
カルボキシアミド)等の2官能以上のアジリジン系化合
物等が挙げられるが、勿論これらに限定されるものでは
ない。
The aziridine compound is a compound having two or more aziridine rings in one molecule, and specifically, N, N'-diphenylmethane-4,4'-bis (1
-Aziridinecarboxamide), trimethylolpropane-tris-β-aziridinylpropionate, N,
Examples thereof include bifunctional or higher-functional aziridine compounds such as N′-hexamethylene-1,6-bis (1-aziridinecarboxamide), but are not limited thereto.

【0017】本発明においては上記アジリジン系化合物
の含有量は、前記アクリル系共重合体の固形分100重
量部に対し0.01〜0.5重量部の範囲にあることが
必要である。アクリル系共重合体の固形分100重量部
に対するアジリジン系化合物の含有量が0.01重量部
未満であると架橋度が低くなるので良好な耐熱性が得ら
れず、逆に0.5重量部を超えると架橋度が高くなり過
ぎ初期接着力が低下する。
In the present invention, the content of the aziridine compound must be in the range of 0.01 to 0.5 parts by weight based on 100 parts by weight of the solid content of the acrylic copolymer. If the content of the aziridine compound is less than 0.01 parts by weight based on 100 parts by weight of the solid content of the acrylic copolymer, the degree of crosslinking will be low and good heat resistance cannot be obtained. If it exceeds, the degree of cross-linking becomes too high and the initial adhesive strength is lowered.

【0018】本発明のアクリル系感圧性接着剤組成物を
構成するアクリル系共重合体の重合方法は特別なもので
はなく、通常の溶液重合法、乳化重合法、分散重合法、
塊状重合法等の公知の重合方法を用いれば良いが、一般
的には溶液重合法が簡便で好適である。
The method of polymerizing the acrylic copolymer constituting the acrylic pressure-sensitive adhesive composition of the present invention is not special, and a usual solution polymerization method, emulsion polymerization method, dispersion polymerization method,
A known polymerization method such as a bulk polymerization method may be used, but a solution polymerization method is generally simple and suitable.

【0019】溶液重合法の場合、例えば、所定の配合の
モノマー類を酢酸エチルのような有機溶剤に所定の濃度
で溶解し、過酸化ベンゾイルや過酸化ラウロイルのよう
な過酸化物を重合触媒として、窒素還流下で攪拌しなが
ら、60〜80℃程度の温度で6〜10時間程度重合反
応を行うことにより所望のアクリル系共重合体溶液を容
易に得ることが出来る。
In the case of the solution polymerization method, for example, monomers having a predetermined composition are dissolved in an organic solvent such as ethyl acetate at a predetermined concentration, and a peroxide such as benzoyl peroxide or lauroyl peroxide is used as a polymerization catalyst. A desired acrylic copolymer solution can be easily obtained by carrying out a polymerization reaction at a temperature of about 60 to 80 ° C. for about 6 to 10 hours while stirring under nitrogen reflux.

【0020】本発明のアクリル系感圧性接着剤組成物に
は、本発明の目的を阻害しない範囲で、可塑剤、軟化
剤、充填剤、染料、顔料、安定剤等の添加剤を適宜含有
させてもよい。
The acrylic pressure-sensitive adhesive composition of the present invention may appropriately contain additives such as a plasticizer, a softening agent, a filler, a dye, a pigment and a stabilizer, as long as the object of the present invention is not impaired. May be.

【0021】本発明の感圧性接着剤組成物で粘着製品を
作成する時の基材に対する塗工厚みは、特に限定される
ものではなく、基材の種類や粘着加工製品の用途にもよ
るが、一般的には乾燥後の膜厚で片面10〜100μm
程度が好ましい。
The coating thickness of the pressure-sensitive adhesive composition of the present invention on a substrate when producing a pressure-sensitive adhesive product is not particularly limited, and depends on the type of the substrate and the use of the pressure-sensitive adhesive processed product. Generally, the film thickness after drying is 10 to 100 μm on one side.
A degree is preferable.

【0022】又、本発明の感圧性接着剤組成物を粘着テ
ープに用いる場合、各種基材の片面のみに感圧性接着剤
層を有する片面粘着テープであっても良いし、又、各種
基材の両面に感圧性接着剤層を有する両面粘着テープで
あっても良い。更にまた、基材を用いないノンサポート
型の粘着テープであっても良い。
When the pressure-sensitive adhesive composition of the present invention is used in a pressure-sensitive adhesive tape, it may be a single-sided pressure-sensitive adhesive tape having a pressure-sensitive adhesive layer on only one side of various base materials, or various base materials. It may be a double-sided pressure-sensitive adhesive tape having pressure-sensitive adhesive layers on both sides. Furthermore, a non-support type adhesive tape that does not use a substrate may be used.

【0023】[0023]

【作用】本発明のアクリル系感圧性接着剤組成物は、架
橋剤としてアジリジン系化合物を用いるので架橋が安定
的且つ速やかに進行するため安定性、生産性に富む。ア
クリル系重合体中及び重合ロジンのペンタエリスリトー
ルエステル中に存在するカルボキシル基とを、架橋剤で
あるアジリジン系化合物を介して結合することにより、
粘着付与樹脂を高分子鎖中に導入し粘着付与樹脂全体の
極性を低めることで低極性被着体に対する接着性が向上
する。又、バルキーな構造を有する粘着付与樹脂を高分
子鎖中に導入するため粘着剤の弾性率を高く設定するこ
とが可能となり、粘着特性、特に耐剥離性を向上させる
ことが可能となる。
In the acrylic pressure-sensitive adhesive composition of the present invention, since the aziridine compound is used as the crosslinking agent, the crosslinking proceeds stably and rapidly, so that the acrylic pressure-sensitive adhesive composition is excellent in stability and productivity. By bonding the carboxyl group present in the acrylic polymer and the pentaerythritol ester of the polymerized rosin through the aziridine compound which is a cross-linking agent,
By introducing the tackifying resin into the polymer chain to reduce the polarity of the tackifying resin as a whole, the adhesion to the low-polar adherend is improved. Further, since the tackifying resin having a bulky structure is introduced into the polymer chain, the elastic modulus of the pressure sensitive adhesive can be set high, and the pressure sensitive adhesive property, especially the peeling resistance can be improved.

【0024】[0024]

【実施例】この発明をさらに詳しく説明するため、以下
に実施例をあげる。なお、実施例中の「部」は「重量
部」を意味する。
EXAMPLES In order to explain the present invention in more detail, examples will be given below. In addition, "part" in an Example means a "weight part."

【0025】(実施例1)(Example 1)

【0026】(a)アクリル系共重合体の重合 温度計、攪拌器及び窒素導入管を備えた反応容器に、表
1の実施例1に示されるように、酢酸エチル100部、
アクリル酸2−エチルヘキシルエステル97部、アクリ
ル酸3部及び連鎖移動剤としてラウリルメルカプタン
0.05部を仕込み、さらに重合開始剤として過酸化ベ
ンゾイル0.1部を添加して窒素還流下で攪拌しながら
80℃−8時間重合反応を行い、固形分50%のアクリ
ル系共重合体溶液を得た。
(A ) As shown in Example 1 in Table 1, 100 parts of ethyl acetate was placed in a reaction vessel equipped with a polymerization thermometer of an acrylic copolymer , a stirrer and a nitrogen inlet tube.
Acrylic acid 2-ethylhexyl ester (97 parts), acrylic acid (3 parts) and lauryl mercaptan (0.05 parts) as a chain transfer agent were added, and benzoyl peroxide (0.1 part) was further added as a polymerization initiator, while stirring under nitrogen reflux. Polymerization reaction was carried out at 80 ° C. for 8 hours to obtain an acrylic copolymer solution having a solid content of 50%.

【0027】(b)アクリル系感圧性接着剤組成物の作
得られたアクリル系共重合体溶液200部(固形分10
0部)に対し、粘着付与樹脂として重合ロジンのペンタ
エリスリトールエステル「ペンセルD160」(融点1
60℃、荒川化学工業社製)10部及び架橋剤として
N,N’−ヘキサメチレン−1,6−ビス(1−アジリ
ジンカルボキシアミド)(商品名「HDU」、相互薬工
社製)0.1部を攪拌混合して固形分52.4%のアク
リル系感圧性接着剤組成物を得た。
( B) Preparation of acrylic pressure-sensitive adhesive composition
Adult resultant acrylic copolymer solution, 200 parts (solid content 10
0 parts), a pentaerythritol ester of polymerized rosin “Pencel D160” as a tackifying resin (melting point 1
60 ° C., manufactured by Arakawa Chemical Industry Co., Ltd.) and 10 parts of N, N′-hexamethylene-1,6-bis (1-aziridinecarboxamide) as a cross-linking agent (trade name “HDU”, manufactured by Mutual Pharmaceutical Co., Ltd.). One part was mixed by stirring to obtain an acrylic pressure-sensitive adhesive composition having a solid content of 52.4%.

【0028】(c)評価 得られたアクリル系感圧性接着剤組成物を剥離紙の離型
処理面に乾燥後の膜厚が65μmとなるように塗工し、
110℃で5分間乾燥した。次いで、この剥離紙上の感
圧性接着剤組成物層を不織布の一方の面と貼り合わせロ
ールで圧着した。さらに不織布の他方の面にも同様の操
作を施し、不織布を基材とする両面粘着テープを得た。
( C) Evaluation The obtained acrylic pressure-sensitive adhesive composition was coated on the release treated surface of the release paper so that the film thickness after drying would be 65 μm,
It was dried at 110 ° C. for 5 minutes. Then, the pressure-sensitive adhesive composition layer on the release paper was bonded to one surface of the non-woven fabric and pressure-bonded with a roll. Further, the same operation was performed on the other surface of the non-woven fabric to obtain a double-sided adhesive tape using the non-woven fabric as a base material.

【0029】得られた両面粘着テープを23℃で24時
間養生した後、該両面粘着テープの各種粘着性能を下記
の方法で評価した結果は表1に示すとおりであった。
The resulting double-sided pressure-sensitive adhesive tape was aged at 23 ° C. for 24 hours, and various adhesive properties of the double-sided pressure-sensitive adhesive tape were evaluated by the following methods.

【0030】初期接着力(対SUS):JIS Z−
1528「両面粘着テープ」に準じ、巾20mm、長さ
100mmに裁断した両面粘着テープを厚さ1.5m
m、巾25mm、長さ100mmの冷間圧延ステンレス
鋼板(SUS304板)に接着長さ75mmで貼り合わ
せ、23℃−65%RHの雰囲気下に20分間放置した
後、テンシロン試験機を用いて引張速度300mm/分
で180度角剥離強度(g/20mm)を測定した。
Initial adhesive strength (against SUS) : JIS Z-
According to 1528 "Double-sided adhesive tape", double-sided adhesive tape cut into a width of 20 mm and a length of 100 mm has a thickness of 1.5 m.
m, width 25 mm, length 100 mm, cold-rolled stainless steel plate (SUS304 plate) with a bonding length of 75 mm, and allowed to stand in an atmosphere of 23 ° C.-65% RH for 20 minutes, then pulled using a Tensilon tester The 180-degree angle peel strength (g / 20 mm) was measured at a speed of 300 mm / min.

【0031】初期接着力(対ポリプロピレン):冷間
圧延ステンレス鋼板の代わりに、厚さ2mm、巾25m
m、長さ100mmのポリプロピレン板を用いたこと以
外は初期接着力(対SUS)の場合と同様にして、1
80度角剥離強度(g/20mm)を測定した。
Initial adhesive strength (against polypropylene) : thickness of 2 mm, width of 25 m instead of cold rolled stainless steel plate
m, the same as the case of the initial adhesive force (against SUS) except that a polypropylene plate with a length of 100 mm was used, 1
The 80-degree angle peel strength (g / 20 mm) was measured.

【0032】保持力(対SUS):JIS Z−15
28に準じ、巾20mm、長さ100mmに裁断した両
面粘着テープを厚さ1.5mm、巾25mm、長さ10
0mmの冷間圧延ステンレス鋼板(SUS304板)に
接着長さ20mmで貼り合わせ、23℃−65%RHの
雰囲気下に20分間、更に80℃の雰囲気下に20分間
放置した後、両面粘着テープを下側にして80℃の恒温
乾燥機中に垂直に懸垂し、両面粘着テープの下端に1k
gの荷重を懸けて垂直に放置し、1時間以内の落下時間
(分)又は1時間後のズレ距離(mm)を測定した。
Holding power (against SUS) : JIS Z-15
According to No. 28, a double-sided pressure-sensitive adhesive tape cut into a width of 20 mm and a length of 100 mm has a thickness of 1.5 mm, a width of 25 mm and a length of 10
A 0 mm cold rolled stainless steel plate (SUS304 plate) was attached with an adhesion length of 20 mm, left in an atmosphere of 23 ° C.-65% RH for 20 minutes, and further in an atmosphere of 80 ° C. for 20 minutes, and then a double-sided adhesive tape was used. Suspend vertically in a constant temperature dryer at 80 ° C and put 1k on the bottom edge of the double-sided adhesive tape.
A load of g was suspended and the sample was left vertically and the dropping time (minute) within 1 hour or the deviation distance (mm) after 1 hour was measured.

【0033】定荷重剥離保持力(対ポリプロピレ
ン):巾20mm、長さ100mmに裁断した両面粘着
テープを厚さ2mm、巾25mm、長さ100mmのポ
リプロピレン板に接着長さ50mmで貼り合わせ、23
℃−65%RHの雰囲気下に20分間放置し、次いで両
面粘着テープを下側にして接着試験片の両端を固定し水
平に置かれた状態で60℃の恒温乾燥機中に20分間放
置した後、両面粘着テープの接着されていない方の端部
に80gの荷重を吊るし90度角剥離方向の荷重を懸け
て、1時間以内の落下時間(分)又は1時間後の剥離距
離(mm)を測定した。
Constant load peeling retention force (against polypropylene
) : A double-sided adhesive tape cut into a width of 20 mm and a length of 100 mm is attached to a polypropylene plate having a thickness of 2 mm, a width of 25 mm and a length of 100 mm with an adhesive length of 50 mm, and 23
20 minutes in an atmosphere of -65% RH, then, with the double-sided adhesive tape on the lower side, both ends of the adhesive test piece were fixed and left horizontally in a constant temperature dryer at 60 ° C for 20 minutes. After that, a load of 80 g is hung on the non-adhesive end of the double-sided pressure-sensitive adhesive tape and a load in the 90 ° angle peeling direction is applied to drop it within 1 hour (minutes) or after 1 hour of peeling distance (mm). Was measured.

【0034】(実施例2〜3)(Examples 2 to 3)

【0035】表1の実施例2及び3に示されるように、
粘着付与樹脂「ペンセルD160」の配合量を変えたこ
と以外は実施例1と同様にして2種類のアクリル系感圧
性接着剤組成物を得た。
As shown in Examples 2 and 3 of Table 1,
Two kinds of acrylic pressure-sensitive adhesive compositions were obtained in the same manner as in Example 1 except that the compounding amount of the tackifying resin "Pencel D160" was changed.

【0036】得られた2種類のアクリル系感圧性接着剤
組成物を実施例1と同様にして評価した結果は表1に示
すとおりであった。
The results of evaluating the two types of acrylic pressure-sensitive adhesive compositions obtained in the same manner as in Example 1 are shown in Table 1.

【0037】(比較例1)(Comparative Example 1)

【0038】表1の比較例1に示されるように、アクリ
ル系共重合体の重合において、モノマー組成をアクリル
酸n−ブチルエステル70部、アクリル酸2−エチルヘ
キシルエステル29.7部及びアクリル酸0.3部とし
たこと以外は実施例1と同様にしてアクリル系感圧性接
着剤組成物を得た。
As shown in Comparative Example 1 in Table 1, in the polymerization of the acrylic copolymer, the monomer composition was 70 parts of acrylic acid n-butyl ester, 29.7 parts of acrylic acid 2-ethylhexyl ester and 0 acrylic acid. An acrylic pressure-sensitive adhesive composition was obtained in the same manner as in Example 1 except that the amount was 0.3 part.

【0039】得られたアクリル系感圧性接着剤組成物を
実施例1と同様にして評価した結果は表1に示すとおり
であった。
The acrylic pressure-sensitive adhesive composition obtained was evaluated in the same manner as in Example 1 and the results are shown in Table 1.

【0040】(比較例2)(Comparative Example 2)

【0041】表1の比較例2に示されるように、アクリ
ル系共重合体の重合において、モノマー組成をアクリル
酸n−ブチルエステル70部、アクリル酸2−エチルヘ
キシルエステル15部及びアクリル酸15部としたこと
以外は実施例1と同様にしてアクリル系感圧性接着剤組
成物を得た。
As shown in Comparative Example 2 of Table 1, in the polymerization of the acrylic copolymer, the monomer composition was 70 parts of acrylic acid n-butyl ester, 15 parts of acrylic acid 2-ethylhexyl ester and 15 parts of acrylic acid. An acrylic pressure-sensitive adhesive composition was obtained in the same manner as in Example 1 except for the above.

【0042】得られたアクリル系感圧性接着剤組成物を
実施例1と同様にして評価した結果は表1に示すとおり
であった。
The results of evaluation of the obtained acrylic pressure-sensitive adhesive composition in the same manner as in Example 1 are shown in Table 1.

【0043】(比較例3〜4)(Comparative Examples 3 to 4)

【0044】表1の比較例3及び4に示されるように、
粘着付与樹脂「ペンセルD160」の配合量を変えたこ
と以外は実施例1と同様にして2種類のアクリル系感圧
性接着剤組成物を得た。
As shown in Comparative Examples 3 and 4 of Table 1,
Two kinds of acrylic pressure-sensitive adhesive compositions were obtained in the same manner as in Example 1 except that the compounding amount of the tackifying resin "Pencel D160" was changed.

【0045】得られた2種類のアクリル系感圧性接着剤
組成物を実施例1と同様にして評価した結果は表1に示
すとおりであった。
The results of evaluating the two types of acrylic pressure-sensitive adhesive compositions obtained in the same manner as in Example 1 are as shown in Table 1.

【0046】(比較例5)(Comparative Example 5)

【0047】表1の比較例5に示されるように、粘着付
与樹脂として「ペンセルD160」の代わりに、不均化
ロジンのペンタエリスリトールエステル「スーパーエス
テルA115」(融点115℃、荒川化学工業社製)を
用いたこと以外は実施例1と同様にしてアクリル系感圧
性接着剤組成物を得た。
As shown in Comparative Example 5 in Table 1, instead of "Pencel D160" as the tackifying resin, pentaerythritol ester "super ester A115" of disproportionated rosin (melting point 115 ° C, manufactured by Arakawa Chemical Industry Co., Ltd. An acrylic pressure-sensitive adhesive composition was obtained in the same manner as in Example 1 except that (1) was used.

【0048】得られたアクリル系感圧性接着剤組成物を
実施例1と同様にして評価した結果は表1に示すとおり
であった。
The results of evaluation of the resulting acrylic pressure-sensitive adhesive composition in the same manner as in Example 1 are shown in Table 1.

【0049】(比較例6〜7)(Comparative Examples 6 to 7)

【0050】表1の比較例6及び7に示されるように、
架橋剤「HDU」の配合量を変えたこと以外は実施例1
と同様にして2種類のアクリル系感圧性接着剤組成物を
得た。
As shown in Comparative Examples 6 and 7 of Table 1,
Example 1 except that the compounding amount of the cross-linking agent "HDU" was changed.
In the same manner as above, two types of acrylic pressure-sensitive adhesive compositions were obtained.

【0051】得られた2種類のアクリル系感圧性接着剤
組成物を実施例1と同様にして評価した結果は表1に示
すとおりであった。
The results of evaluating the two types of acrylic pressure-sensitive adhesive compositions obtained in the same manner as in Example 1 are as shown in Table 1.

【0052】(比較例8)(Comparative Example 8)

【0053】表1の比較例8に示されるように、架橋剤
として「HDU」の代わりに、イソシアネート系化合物
「コロネートL」(有効成分55%、日本ポリウレタン
工業社製)を用い、固形分でアクリル系共重合体100
部に対し「コロネートL」2部を配合したこと以外は実
施例1と同様にしてアクリル系感圧性接着剤組成物を得
た。
As shown in Comparative Example 8 in Table 1, the isocyanate compound "Coronate L" (active ingredient 55%, manufactured by Nippon Polyurethane Industry Co., Ltd.) was used as a cross-linking agent in place of "HDU", and in solid content. Acrylic copolymer 100
An acrylic pressure-sensitive adhesive composition was obtained in the same manner as in Example 1 except that 2 parts of "Coronate L" was added to each part.

【0054】得られたアクリル系感圧性接着剤組成物を
実施例1と同様にして評価した結果は表1に示すとおり
であった。
The results of evaluation of the obtained acrylic pressure-sensitive adhesive composition in the same manner as in Example 1 are shown in Table 1.

【0055】[0055]

【表1】 [Table 1]

【0056】[0056]

【発明の効果】以上述べたように、本発明のアクリル系
感圧性接着剤組成物は、低極性被着体に対する接着力、
特に耐剥離性に優れるので、広範囲の用途の粘着加工製
品に好適に使用出来るものである。
As described above, the acrylic pressure-sensitive adhesive composition of the present invention has an adhesive force to a low-polar adherend,
In particular, since it has excellent peeling resistance, it can be suitably used for adhesive processed products for a wide range of applications.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 アルキル基の炭素数が2〜18の(メ
タ)アクリル酸アルキルエステル99.5〜90重量%
と重合性不飽和カルボン酸0.5〜10重量%とを共重
合して得られるアクリル系共重合体の固形分100重量
部に対し、重合ロジンのペンタエリスリトールエステル
5〜40重量部及び1分子中に2個以上のアジリジン環
を有するアジリジン系化合物0.01〜0.5重量部が
含有されていることを特徴とするアクリル系感圧性接着
剤組成物。
1. 99.5 to 90% by weight of a (meth) acrylic acid alkyl ester in which the alkyl group has 2 to 18 carbon atoms.
5 to 40 parts by weight and one molecule of pentaerythritol ester of polymerized rosin, based on 100 parts by weight of solid content of the acrylic copolymer obtained by copolymerizing 0.5 to 10% by weight of polymerizable unsaturated carboxylic acid. An acrylic pressure-sensitive adhesive composition containing 0.01 to 0.5 part by weight of an aziridine compound having two or more aziridine rings.
JP28902393A 1993-11-18 1993-11-18 Pressure-sensitive acrylic adhesive composition Pending JPH07138544A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28902393A JPH07138544A (en) 1993-11-18 1993-11-18 Pressure-sensitive acrylic adhesive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28902393A JPH07138544A (en) 1993-11-18 1993-11-18 Pressure-sensitive acrylic adhesive composition

Publications (1)

Publication Number Publication Date
JPH07138544A true JPH07138544A (en) 1995-05-30

Family

ID=17737831

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28902393A Pending JPH07138544A (en) 1993-11-18 1993-11-18 Pressure-sensitive acrylic adhesive composition

Country Status (1)

Country Link
JP (1) JPH07138544A (en)

Cited By (11)

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Publication number Priority date Publication date Assignee Title
US5935711A (en) * 1996-10-23 1999-08-10 3M Innovative Properties Company Organoborane amine complex initiator systems and polymerizable compositions made therewith
US6383655B1 (en) 1998-06-12 2002-05-07 3M Innovative Properties Company Low odor polymerizable compositions useful for bonding low surface energy substrates
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US8148471B2 (en) 2009-11-23 2012-04-03 3M Innovative Properties Company Acrylic pressure-sensitive adhesives with aziridinyl-epoxy crosslinking system
JP2013504664A (en) * 2009-09-11 2013-02-07 エイブリィ デニソン コーポレーション Double cross-linked tackifying pressure sensitive adhesive
US8420214B2 (en) 2008-06-09 2013-04-16 3M Innovative Properties Company Acrylic pressure-sensitive adhesives with aziridine crosslinking agents
US8507612B2 (en) 2009-03-09 2013-08-13 3M Innovative Properties Company Aziridine crosslinking agents for acrylic adhesives
US8524836B2 (en) 2010-01-20 2013-09-03 3M Innovative Properties Company Crosslinkable acrylate adhesive polymer composition
JP2015110724A (en) * 2013-11-07 2015-06-18 積水化学工業株式会社 Adhesive tape
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Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5935711A (en) * 1996-10-23 1999-08-10 3M Innovative Properties Company Organoborane amine complex initiator systems and polymerizable compositions made therewith
US6383655B1 (en) 1998-06-12 2002-05-07 3M Innovative Properties Company Low odor polymerizable compositions useful for bonding low surface energy substrates
US7189303B2 (en) 1998-06-12 2007-03-13 3M Innovative Properties Company Initiator systems and adhesive compositions made therewith
US6812308B2 (en) 2000-11-21 2004-11-02 3M Innovative Properties Company Initiator systems and adhesive compositions made therewith
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WO2003099954A3 (en) * 2002-05-20 2004-03-11 3M Innovative Properties Co Pressure sensitive adhesive composition, articles made therewith and method of use
US6893718B2 (en) 2002-05-20 2005-05-17 3M Innovative Properties Company Pressure sensitive adhesive composition, articles made therewith and method of use
US8420214B2 (en) 2008-06-09 2013-04-16 3M Innovative Properties Company Acrylic pressure-sensitive adhesives with aziridine crosslinking agents
US8507612B2 (en) 2009-03-09 2013-08-13 3M Innovative Properties Company Aziridine crosslinking agents for acrylic adhesives
JP2013504664A (en) * 2009-09-11 2013-02-07 エイブリィ デニソン コーポレーション Double cross-linked tackifying pressure sensitive adhesive
US9321938B2 (en) 2009-09-11 2016-04-26 Avery Dennison Corporation Dual crosslinked tackified pressure sensitive adhesive
US8148471B2 (en) 2009-11-23 2012-04-03 3M Innovative Properties Company Acrylic pressure-sensitive adhesives with aziridinyl-epoxy crosslinking system
US8524836B2 (en) 2010-01-20 2013-09-03 3M Innovative Properties Company Crosslinkable acrylate adhesive polymer composition
JP2015110724A (en) * 2013-11-07 2015-06-18 積水化学工業株式会社 Adhesive tape
CN111777959A (en) * 2020-07-10 2020-10-16 广东弘擎电子材料科技有限公司 Polyurethane foaming double-sided adhesive tape and preparation method thereof
CN111777959B (en) * 2020-07-10 2022-07-29 广东弘擎电子材料科技有限公司 Polyurethane foaming double-sided adhesive tape and preparation method thereof

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