JPH0142984B2 - - Google Patents

Info

Publication number
JPH0142984B2
JPH0142984B2 JP60112679A JP11267985A JPH0142984B2 JP H0142984 B2 JPH0142984 B2 JP H0142984B2 JP 60112679 A JP60112679 A JP 60112679A JP 11267985 A JP11267985 A JP 11267985A JP H0142984 B2 JPH0142984 B2 JP H0142984B2
Authority
JP
Japan
Prior art keywords
polyvinyl acetate
glycidyl ether
degree
parts
treatment agent
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.)
Expired
Application number
JP60112679A
Other languages
Japanese (ja)
Other versions
JPS61271372A (en
Inventor
Kihachi Suzuki
Hiroshi Yamamoto
Takanobu Tomomoto
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 JP60112679A priority Critical patent/JPS61271372A/en
Publication of JPS61271372A publication Critical patent/JPS61271372A/en
Publication of JPH0142984B2 publication Critical patent/JPH0142984B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Adhesive Tapes (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明は、ポリ酢酸ビニル―長鎖アルキルグリ
シジルエーテル系の親水性基材に対しても接着性
にすぐれる剥離性処理剤に関するものである。 従来の技術 基材の片面に粘着剤層を設けてなる粘着テープ
のように巻重物の形態で保存され、使用時にこれ
を巻戻すものにあつてはその自背面よりの巻戻し
を容易とするために、基材の背面に剥離性処理剤
からなる剥離性処理層が設けられている。 この剥離性処理剤に要求される一般的性能とし
ては種々あるなかでも殊に、その剥離性処理層が
基材より脱落しないこと(接着性)、該処理層中
の成分が粘着剤側に移行して糊面を汚染しないこ
と(糊面の接着力低減の防止性)、糊面との接着
性と剥離性とが適度にバランスしていて巻重テー
プのタケノコ現象等の形態くずれや粘着剤の基材
背面側への移行現象を起さないことが重要であ
る。 従来、その剥離性処理剤としては加熱硬化型シ
リコーン系のもの、オクタデシルアクリレート―
アクリル酸共重合体系のもの(特公昭29−3144号
公報)、ポリビニルアルコール―オクタデシルイ
ソシアネート系のもの(特公昭29−7333号公報)、
ポリビニルアルコール―オクタデシルイソシアネ
ート―多官能性イソシアネート系のもの(特開昭
54−56638号公報)などが知られていた。 発明が解決しようとする問題点 しかしながら、加熱硬化型シリコーン系のもの
にはその処理層が剥離性に勝り過ぎて、重ね貼り
不能や巻重物の形態くずれなどの問題があり、オ
クタデシルアクリレート―アクリル酸共重合体系
のもの及びポリビニルアルコール―オクタデシル
イソシアネート系のものには、セルロース系フイ
ルムのような親水性基材に対する接着性に劣つて
その処理層が基材より脱落するという問題があつ
た。一方、前記オクタデシルイソシアネート系の
ものの該親水性基材に対する接着不良性を改善し
たものとして提案されているポリビニルアルコー
ル―オクタデシルイソシアネート―多官能性イソ
シアネート系のものには接着性に勝つて剥離に要
する力が大きいという問題があつた。 問題点を解決するための手段 本発明者らは上記の問題を克服し、親水性基材
に対ても満足できる接着性を有し、かつ、基材背
面―粘着剤表面間における剥離―接着バランスに
すぐれる処理層を形成できる剥離性処理剤を開発
するために鋭意研究を重ねた結果、ポリ酢酸ビニ
ル―長鎖アルキルグリシジルエーテル系のものに
よりその目的を達成しうることを見出し、本発明
をなすに至つた。 すなわち、本発明は、ケン化系ポリ酢酸ビニル
と長鎖アルキルグリシジルエーテルとの反応生成
物からなる剥離性処理剤を提供するものである。 本発明において用いられるケン化系ポリ酢酸ビ
ニルとしてはケン化度が30〜90%のものが好まし
い。ケン化度が過少のものであると得られる剥離
性処理剤による処理層が剥離性に乏しいものとな
り、他方過多のものであると反応完結性に劣つて
均一な反応生成物が得にくくなる。また、ケン化
系ポリ酢酸ビニルとしては平均重合度が100〜
3000のものが好ましい。その平均重合度が過少の
ものであると得られる剥離性処理剤による処理層
が耐熱性に劣るものとなり、他方過多のものであ
ると反応性、溶解性に劣つて実用上好ましくな
い。 本発明において用いられ、一般式
INDUSTRIAL APPLICATION FIELD The present invention relates to a releasable treatment agent that exhibits excellent adhesion even to polyvinyl acetate-long chain alkyl glycidyl ether-based hydrophilic substrates. PRIOR TECHNOLOGY When an adhesive tape is stored in the form of a roll, such as an adhesive tape with an adhesive layer on one side of a base material, and is unwound when used, it is easy to unwind it from its own back side. In order to do this, a releasable treatment layer made of a releasable treatment agent is provided on the back side of the base material. Among the various general performances required of this releasable treatment agent, in particular, the releasable treatment layer does not fall off from the base material (adhesion), and the components in the treatment layer migrate to the adhesive side. It does not contaminate the adhesive surface (prevents reduction in adhesive strength on the adhesive surface), and has a suitable balance between adhesion and peelability to the adhesive surface, preventing deformation such as bamboo shoot phenomenon of rolled tape and adhesive. It is important that no migration phenomenon occurs to the back side of the base material. Conventionally, the releasable treatment agents used are heat-curing silicone-based ones and octadecyl acrylate.
Acrylic acid copolymer-based products (Japanese Patent Publication No. 29-3144), polyvinyl alcohol-octadecyl isocyanate-based products (Japanese Patent Publication No. 7333-1987),
Polyvinyl alcohol-octadecyl isocyanate-polyfunctional isocyanate type (JP-A-Sho
54-56638) were known. Problems to be Solved by the Invention However, heat-curable silicone-based products have problems such as the treatment layer having too much releasability, making it impossible to apply multiple layers and deforming rolled products.Octadecyl acrylate-acrylic Acid copolymer-based materials and polyvinyl alcohol-octadecyl isocyanate-based materials have a problem in that they have poor adhesion to hydrophilic substrates such as cellulose films, resulting in the treated layer falling off from the substrate. On the other hand, polyvinyl alcohol-octadecyl isocyanate-polyfunctional isocyanate-based products, which have been proposed to improve the poor adhesion of the octadecyl isocyanate-based products to the hydrophilic substrate, overcome the adhesion and have the force required for peeling. The problem was that it was large. Means for Solving the Problems The present inventors have overcome the above problems, have satisfactory adhesion even to hydrophilic substrates, and have peeling-adhesion between the back surface of the substrate and the surface of the adhesive. As a result of extensive research in order to develop a releasable treatment agent that can form a well-balanced treatment layer, it was discovered that the objective could be achieved with a polyvinyl acetate-long chain alkyl glycidyl ether type agent, and the present invention was developed. I was able to accomplish this. That is, the present invention provides a stripping treatment agent comprising a reaction product of saponified polyvinyl acetate and a long-chain alkyl glycidyl ether. The saponified polyvinyl acetate used in the present invention preferably has a degree of saponification of 30 to 90%. If the degree of saponification is too low, the layer treated with the releasable treatment agent obtained will have poor releasability, while if it is too high, the reaction completion will be poor and it will be difficult to obtain a uniform reaction product. In addition, as saponified polyvinyl acetate, the average degree of polymerization is 100~
3000 is preferred. If the average degree of polymerization is too low, the resulting layer treated with the release treatment agent will have poor heat resistance, while if it is too high, the reactivity and solubility will be poor, which is not preferred in practice. Used in the present invention, the general formula

【式】 (Rはアルキル基で ある) で表わされる長鎖アルキルグリシジルエーテルと
しては、例えばヘキサデシルグリシジルエーテ
ル、ヘプタデシルグリシジルエーテル、オクタデ
シルグリシジルエーテル、ノナデシルグリシジル
エーテル、エイコシルグリシジルエーテルなどで
代表されるアルキル基の炭素数が16〜20のものが
望ましい。 本発明の剥離性処理剤は、例えば有機溶媒中、
アルカリの存在下に加熱してケン化系ポリ酢酸ビ
ニルに長鎖アルキルグリシジルエーテルをそのグ
リシジル基を介してグラフト化反応させるなどし
て得られる、ケン化系ポリ酢酸ビニルと長鎖アル
キルグリシジルエーテルとの反応生成物からなる
ものである。この剥離性処理剤による処理層の剥
離性、ひいては剥離―接着バランス性は長鎖アル
キルグリシジルエーテルの導入割合によりントロ
ールされる。一方、長鎖アルキルグリシジルエー
テルの導入割合はケン化系ポリ酢酸ビニルのケン
化度と、このポリ酢酸ビニルに対する長鎖アルキ
ルグリシジルエーテルの反応時における配合割合
により決定される。本発明においては該ポリ酢酸
ビニルのケン化基に対し該エーテルを当量的に用
い、該エーテルの導入割合を該ポリ酢酸ビニルに
おけるケン化度でコントロールする反応方式が得
られる剥離性処理剤による処理層の親水性基材に
対する接着性などの物性ないし性能の点で望まし
い。この観点よりも反応に際して用いる該ポリ酢
酸ビニルのケン化度は30〜90%が適当である。 本発明の剥離性処理剤の基材に対する適用は、
例えば有機溶媒溶液とするなどして行われる。 発明の効果 本発明のポリ酢酸ビニル―長鎖アルキルグリシ
ジルエーテル系の剥離性処理剤によれば、例えば
セロハン系基材、ポリビニルアルコール系基材の
ような親水性基材に対しても接着性(投錨性)に
すぐれて基材より脱落しにくく、かつ、剥離―接
着バランス性にもすぐれる剥離性処理層を形成す
ることができる。 実施例 実施例 1 還流冷却器を付設した三ツ口フラスコにケン化
度88%、平均重合度500のポリ酢酸ビニル20部
(重量部、以下同様)とキシレン205部とを入れて
120℃に加温したのち水酸化カリウムのキシレン
溶液を少量加えて系をアルカリ性とし、これにオ
クタデシルグリシジルエーテル117部を加えて10
時間反応を行わせ、目的生成物としての剥離性処
理剤を得た。 実施例 2〜5 ケン化度88%、平均重合度1400のポリ酢酸ビニ
ル20部とオクタデシルグリシジルエーテル117部
(実施例2)、 ケン化度88%、平均重合度2300のポリ酢酸ビニ
ル20部とオクタデシルグリシジルエーテル117部
(同3)、 ケン化度80%、平均重合度500のポリ酢酸ビニ
ル20部とエイコシルグリシジルエーテル105部
(同4)、 ケン化度38%、平均重合度1400のポリ酢酸ビニ
ル20部とエイコシルグリシジルエーテル38部(同
5)を用いたほかは実施例1に準じて剥離性処理
剤を得た。 比較例 1、2 ケン化度88%、平均重合度500のポリ酢酸ビニ
ル20部とオクタデシルイソシアネート105部(比
較例1)、 ケン化度88%、平均重合度1400のポリ酢酸ビニ
ル20部とオクタデシルイソシアネート105部(同
2)を用いたほかは実施例1に準じて剥離性処理
剤を得た。 評価試験 実施例、比較例で得た剥離性処理剤を含有する
反応液にトルエンを加えて固形分1重量%の溶液
とし、これをセロハンフイルムの片面に0.05g/
m2の塗布量になるように塗布し乾燥させて剥離性
処理フイルムを得た。 次に、その剥離性処理フイルムの処理面にポリ
エステル粘着テープ(日東電気工業社製、No.
31B)を、2Kgローラを1往復させることにより
圧着させたのち常態で該粘着テープを180度ピー
ル方式で引き剥がし、その際の剥離力を測定し
た。 一方、該フイルムの処理面を指で摩擦すること
により処理層の基材よりの脱落性を調べた。そし
て、脱落が全くない場合を〇、脱落があつた場合
を×として評価した。結果を表に示した。
[Formula] (R is an alkyl group) Long chain alkyl glycidyl ethers include, for example, hexadecyl glycidyl ether, heptadecyl glycidyl ether, octadecyl glycidyl ether, nonadecyl glycidyl ether, eicosyl glycidyl ether, etc. It is desirable that the alkyl group has 16 to 20 carbon atoms. The strippable treatment agent of the present invention can be used, for example, in an organic solvent.
Saponified polyvinyl acetate and long chain alkyl glycidyl ether obtained by heating in the presence of an alkali to graft a long chain alkyl glycidyl ether onto saponified polyvinyl acetate via its glycidyl group. It consists of the reaction product of The releasability of the treated layer using this releasable treatment agent, and ultimately the release-adhesion balance, is controlled by the proportion of long-chain alkyl glycidyl ether introduced. On the other hand, the introduction ratio of the long-chain alkyl glycidyl ether is determined by the degree of saponification of the saponified polyvinyl acetate and the blending ratio of the long-chain alkyl glycidyl ether to the polyvinyl acetate during the reaction. In the present invention, the ether is used in an equivalent amount to the saponification group of the polyvinyl acetate, and the treatment with a stripping agent provides a reaction method in which the introduction ratio of the ether is controlled by the degree of saponification of the polyvinyl acetate. It is desirable in terms of physical properties and performance such as adhesion of the layer to the hydrophilic base material. From this point of view, it is appropriate that the degree of saponification of the polyvinyl acetate used in the reaction is from 30 to 90%. Application of the releasable treatment agent of the present invention to a base material is as follows:
For example, it is carried out as an organic solvent solution. Effects of the Invention According to the polyvinyl acetate-long chain alkyl glycidyl ether-based releasable treatment agent of the present invention, adhesiveness ( It is possible to form a releasable treated layer that has excellent anchoring properties), is difficult to fall off from the base material, and has excellent peel-adhesion balance. Examples Example 1 In a three-necked flask equipped with a reflux condenser, 20 parts of polyvinyl acetate (parts by weight, hereinafter the same) with a degree of saponification of 88% and an average degree of polymerization of 500 and 205 parts of xylene were placed.
After heating to 120°C, a small amount of xylene solution of potassium hydroxide was added to make the system alkaline, and 117 parts of octadecyl glycidyl ether was added to make the system alkaline.
The reaction was carried out for a period of time to obtain a stripping treatment agent as the desired product. Examples 2 to 5 20 parts of polyvinyl acetate with a degree of saponification of 88% and an average degree of polymerization of 1400 and 117 parts of octadecyl glycidyl ether (Example 2), 20 parts of polyvinyl acetate with a degree of saponification of 88% and an average degree of polymerization of 2300 117 parts of octadecyl glycidyl ether (3), 20 parts of polyvinyl acetate with a degree of saponification of 80% and an average degree of polymerization of 500, and 105 parts of eicosyl glycidyl ether (4), a polyvinyl acetate with a degree of saponification of 80% and an average degree of polymerization of 1400. A stripping agent was obtained in the same manner as in Example 1, except that 20 parts of vinyl acetate and 38 parts of eicosyl glycidyl ether (5 parts) were used. Comparative Examples 1 and 2 20 parts of polyvinyl acetate with a degree of saponification of 88% and an average degree of polymerization of 500 and 105 parts of octadecyl isocyanate (Comparative Example 1), 20 parts of polyvinyl acetate with a degree of saponification of 88% and an average degree of polymerization of 1400 and octadecyl A stripping agent was obtained in the same manner as in Example 1, except that 105 parts of isocyanate (same as 2) was used. Evaluation test Toluene was added to the reaction solution containing the strippable treatment agent obtained in the Examples and Comparative Examples to make a solution with a solid content of 1% by weight, and 0.05 g/g of this was applied to one side of a cellophane film.
A releasable treated film was obtained by applying the coating to a coating amount of m 2 and drying it. Next, polyester adhesive tape (manufactured by Nitto Electric Industry Co., Ltd., No.
31B) was pressed by making one reciprocation with a 2 kg roller, and then the adhesive tape was peeled off in a normal state using a 180 degree peel method, and the peeling force at that time was measured. On the other hand, the ability of the treated layer to fall off from the base material was examined by rubbing the treated surface of the film with a finger. The case where there was no falling off was evaluated as ○, and the case where there was some falling off was evaluated as ×. The results are shown in the table.

【表】 表より実施例の本発明の剥離性処理剤による処
理層は、基材に対する接着性及び剥離―接着バラ
ンスにすぐれていることがわかる。
[Table] It can be seen from the table that the layer treated with the releasable treatment agent of the present invention in Examples has excellent adhesion to the substrate and excellent release-adhesion balance.

Claims (1)

【特許請求の範囲】 1 ケン化系ポリ酢酸ビニルと長鎖アルキルグリ
シジルエーテルとの反応生成物からなる剥離性処
理剤。 2 ケン化系ポリ酢酸ビニルがケン化度30〜90%
のものである特許請求の範囲第1項記載の処理
剤。 3 ケン化系ポリ酢酸ビニルが平均重合度100〜
3000のものである特許請求の範囲第1項記載の処
理剤。 4 長鎖アルキルグリシジルエーテルにおけるア
ルキル基が炭素数16〜20のものである特許請求の
範囲第1項記載の処理剤。
[Scope of Claims] 1. A stripping treatment agent comprising a reaction product of saponified polyvinyl acetate and long-chain alkyl glycidyl ether. 2 Saponified polyvinyl acetate has a saponification degree of 30-90%
The processing agent according to claim 1, which is a treatment agent according to claim 1. 3 Saponified polyvinyl acetate has an average degree of polymerization of 100~
3000. The processing agent according to claim 1. 4. The processing agent according to claim 1, wherein the alkyl group in the long-chain alkyl glycidyl ether has 16 to 20 carbon atoms.
JP60112679A 1985-05-24 1985-05-24 Strippable treating agent Granted JPS61271372A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60112679A JPS61271372A (en) 1985-05-24 1985-05-24 Strippable treating agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60112679A JPS61271372A (en) 1985-05-24 1985-05-24 Strippable treating agent

Publications (2)

Publication Number Publication Date
JPS61271372A JPS61271372A (en) 1986-12-01
JPH0142984B2 true JPH0142984B2 (en) 1989-09-18

Family

ID=14592759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60112679A Granted JPS61271372A (en) 1985-05-24 1985-05-24 Strippable treating agent

Country Status (1)

Country Link
JP (1) JPS61271372A (en)

Also Published As

Publication number Publication date
JPS61271372A (en) 1986-12-01

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