JPS61126191A - Three-component releasable treatment layer - Google Patents
Three-component releasable treatment layerInfo
- Publication number
- JPS61126191A JPS61126191A JP59247148A JP24714884A JPS61126191A JP S61126191 A JPS61126191 A JP S61126191A JP 59247148 A JP59247148 A JP 59247148A JP 24714884 A JP24714884 A JP 24714884A JP S61126191 A JPS61126191 A JP S61126191A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- copolymer
- long
- releasable
- 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
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- Laminated Bodies (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Adhesive Tapes (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔利用分野〕
本発明は、水溶性ポリエステV樹脂と長鎖アMキル系化
合物と特殊な共重合体からなり、基材殊にホlJエステ
V系基材に対する接着性に優れて、剥離性をコントロー
ルすることができる新規で剥離剤として好適な剥離性処
理剤からなる剥離性処理りに関するものである。Detailed Description of the Invention [Field of Application] The present invention consists of a water-soluble polyester V resin, a long-chain alkyl compound, and a special copolymer, and is suitable for adhesion to substrates, especially HolJ Esthe V-based substrates. The present invention relates to a releasability treatment comprising a new releasability treatment agent suitable as a release agent, which has excellent properties and can control releasability.
粘着テープやラベル等における粘着面を保護ないし保存
する目的で剥離紙が用いられている。剥離紙は一般にグ
ラシン紙やクラフト紙などからなる紙基材、あるいはポ
リエステルフィルムなどからなる1フスナツクフイルム
等に、剥離性を付与するための剥離剤ないし剥離性処理
剤からなる蟹を設けたものよりなっている。Release paper is used to protect or preserve the adhesive surface of adhesive tapes, labels, etc. Release paper is generally a paper base material such as glassine paper or kraft paper, or a film made of polyester film, etc., which is provided with a release agent or release treatment agent to impart release properties. It's getting better.
ところで、剥離紙には機械的衝撃力によって剥離性処理
層が基材より簡単に脱落しない程度の基材に対する接着
力と、その剥離紙を粘着剤等の粘着性物質より引き剥す
際に剥離性処理剤の粘着性物質層への移着あるいは粘着
性物質の剥離性処理智への移行などを伴わすに手軽に引
き剥せる程度の剥離性とが姿求される。By the way, the release paper has enough adhesion to the base material to prevent the releasable treated layer from easily falling off from the base material due to mechanical impact force, and a releasability that is sufficient to prevent the release paper from falling off from the base material when the release paper is peeled off from a sticky substance such as an adhesive. Releasability to the extent that the treatment agent can be easily peeled off is desired due to the transfer of the treatment agent to the adhesive substance layer or the transfer of the adhesive substance to the releasability treatment layer.
従来、その剥離紙を形成するための剥離住処′理剤とし
ては、エチレン尿素基又はN−メチロール基を有する長
鎖アルキル化合物が知られていた(特開昭52−688
5号公報、特開昭52−788:13号公報)。Conventionally, long-chain alkyl compounds having an ethylene urea group or an N-methylol group have been known as release treatment agents for forming the release paper (Japanese Patent Laid-Open No. 52-688).
No. 5, JP-A-52-788:13).
しかしながら、上記発明の剥離性処理剤ではポリエステ
ルフィルム等のポリエステル糸基材に対しては満足でき
る十分な接着力を有していなかった。However, the releasable treatment agent of the above invention did not have sufficient adhesion to polyester thread base materials such as polyester films.
すなわち、これをポリエステル系基材に適用した場合そ
の接着力に劣って、形成された剥離性処理層が基材より
簡単に脱落し、基材に対する接着力と粘着剤等からの剥
離性のバランス性に劣るという問題があまた。そのため
、この剥離性処理層を設けたポリエステル系基材からな
る剥離材にあってはこれを粘着テープやラベル等に貼付
け、その後剥がしたときに剥離性処理剤が粘着性物質V
−の面に移着して、粘着テープやヲベV等の接着力が低
下するなどの不都合が6つ九。In other words, when this is applied to a polyester base material, its adhesive strength is poor, and the formed releasable treated layer easily falls off from the base material, resulting in a balance between adhesive strength to the base material and releasability from adhesives, etc. There is also the problem of being inferior in gender. Therefore, in the case of a release material made of a polyester base material provided with this releasable treatment layer, when it is attached to an adhesive tape or label, etc., and then peeled off, the releasability treatment agent is removed from the adhesive substance V.
There are six nine inconveniences, such as the adhesion of adhesive tapes and tapes, etc., decreasing due to adhesion to the - side.
本発明者らは、上記の問題点を克服し、ポリエステV系
基材に対しても満足できる接着力を有し、かつ、剥離性
とのバランス性にも優れ、しかも剥離性を適宜にコント
ロールできる剥離性処理剤からなる処環豐を開発するた
めに鋭意研究を重ねた結果、水溶性ポリエステル樹脂と
長鎖アルキル系化合物と特殊な共重合体からなるものに
よりその目的を達成しうろことを見出し、本発明をなす
に至った。The present inventors have overcome the above problems, have satisfactory adhesion even to polyester V-based substrates, have excellent balance with releasability, and can control releasability as appropriate. As a result of intensive research to develop a releasable treatment agent, it was discovered that this objective could be achieved with a product consisting of a water-soluble polyester resin, a long-chain alkyl compound, and a special copolymer. This finding led to the present invention.
すなわち、本発明は体)水溶性ポリエステル樹脂100
重量部、β)エチレン尿素基又はN−メチロール基を有
する長鎖アVキV化合物5〜100重量部、0カルボキ
シル基を有する単量体とこれとは別種の単量体との共重
合体30〜800重量部及びO液媒体からなる剥離性処
理剤で形成されてなる剥離性処理II!を提供するもの
である。That is, the present invention is based on water-soluble polyester resin 100
Parts by weight, β) 5 to 100 parts by weight of a long-chain A-V compound having an ethylene urea group or an N-methylol group, a copolymer of a monomer having 0 carboxyl groups and a different type of monomer Peelability treatment II formed with a peelability treatment agent consisting of 30 to 800 parts by weight and an O liquid medium! It provides:
本発明において水溶性ポリエステル樹脂樹脂■は、主に
基材殊にポリエステル系基材に対する接着力は与剤とし
て、長鎖アIレキル系化合物に)は主に剥離性は与剤と
して、該共重合体(Qけ主に長鎖アMキIし系化合物の
捕獲剤として用いられる。また、水溶性ytFIJエス
テ〜樹脂は水液系の処理剤の調製を可能とするためにも
用いられている。剥離性処理剤を水液系のものとするこ
とにより、公害、爆発・火災などを回避できること、有
機溶剤の回収が不要となって生産労力を低減できること
、基材の劣化を防止できることなどの利点がある。In the present invention, the water-soluble polyester resin (1) is mainly used as an agent to provide adhesion to the base material, particularly to the polyester base material, and is used as an agent to provide long-chain alexyl compounds (2) to the long-chain alexyl compound, mainly to provide release properties. Polymers (Q) are mainly used as capture agents for long-chain A/M compounds.Water-soluble ytFIJ resins are also used to enable the preparation of aqueous treatment agents. By using a water-based stripping treatment agent, pollution, explosions, fires, etc. can be avoided, there is no need to recover organic solvents, reducing production labor, and deterioration of the base material can be prevented. There are advantages.
一方、剥離性処理剤における長鎖アMキM系化合物の配
合割合を変えることにより、基材に対する接着力と粘着
性物質からの剥離性とのバランスが調節でれる。すなわ
ち、液媒体を介して各成分(A、B及びC)を混合して
なる本発明における剥離性処理剤を基材に塗布し、これ
を乾燥させて形成した剥離性処理層は、その乾燥過程に
おける相分離現象に起因して、該共重合体における力V
ボキシV基と反応した長鎖アルキル系化合物が該処理層
の表面側に多く分布する層状態から水溶性ポリエステル
樹脂曹中に点在する善状態までその長鎖アVキV系化合
物の含有割合に基づいて変化し、これにより接着力と剥
離性とのバランスが変化する。その結果、接着力と剥離
性とのバランスのコントロールが可能となる。On the other hand, by changing the blending ratio of the long-chain A/M compound in the releasable treatment agent, the balance between adhesive strength to the substrate and releasability from the adhesive substance can be adjusted. That is, the releasable treatment layer formed by applying the releasable treatment agent of the present invention, which is formed by mixing each component (A, B, and C) through a liquid medium to a base material and drying it, Due to the phase separation phenomenon in the process, the force V in the copolymer
The content ratio of long-chain alkyl-based compounds ranging from a layer state in which the long-chain alkyl-based compounds reacted with the boxy V group are largely distributed on the surface side of the treated layer to a good state in which they are scattered throughout the water-soluble polyester resin. This changes the balance between adhesive strength and releasability. As a result, it becomes possible to control the balance between adhesive strength and releasability.
本発明において用いられる水溶性ポリエステル樹脂(3
)は、例えばテレフタル酸、トリメリット酸のような多
塩基酸と、エチレング17コー〃、グリセリンのような
多価アルコ−Vとの縮合反応生成物であるポリエステル
樹脂を硫酸、発!!硫酸、三酸化イオウのようなスMホ
ン化剤でそのベンゼン環をスルホン化し、これを水酸化
ナトリウム水溶液、水酸化カリウム水溶液、アンモニア
水のような中和剤で中和して水溶性のものとしたものな
どをあげることができる。その具体例としては、「ガグ
センEI9−903J、「ガ1センES−904J、「
ガブセンE8−905J、「ガプセンE8−2011J
(いずれも商品名:帝国化学産業社製)などをあげるこ
とができる。本発明においては、25重量%水溶液とし
た場合にその25°Cにおける粘度が100〜1011
011七ンチボイズ、なかんずく200〜8000セン
チポイズとなるものが、得られる剥離性処理剤の塗工性
、形成される剥離性処理−の物性(接着力と剥離性との
バランス性など)、殊にポリエステル系基材に適用した
場合のその物性などの点で好ましく用いられる。Water-soluble polyester resin used in the present invention (3
) is a polyester resin, which is a condensation reaction product of a polybasic acid such as terephthalic acid or trimellitic acid, and a polyhydric alcohol such as ethylene glycol or glycerin. ! The benzene ring is sulfonated with a sulfonating agent such as sulfuric acid or sulfur trioxide, and this is neutralized with a neutralizing agent such as an aqueous sodium hydroxide solution, an aqueous potassium hydroxide solution, or aqueous ammonia to create a water-soluble product. You can give examples such as: Specific examples include "Gagsen EI9-903J,""GagsenES-904J,"
Gabsen E8-905J, “Gabsen E8-2011J
(Both product names: Teikoku Kagaku Sangyo Co., Ltd.). In the present invention, when it is made into a 25% by weight aqueous solution, the viscosity at 25°C is 100 to 1011.
011 Seven centipoise, especially those with 200 to 8000 centipoise, are the coating properties of the resulting release treatment agent, the physical properties of the release treatment to be formed (balance between adhesive strength and releasability, etc.), especially polyester It is preferably used in terms of its physical properties when applied to a base material.
一方、長鎖アルキル化合物(ロ)としては下記する共重
合体と反応させるためにエチレン尿素基又はN−メチロ
ール基を有するものが用いられる。この化合物における
長鎖アシキル基は、その炭素数が16〜24であること
が得られる剥離性処理剤の性状、形成される剥離性処理
すの物性などの点で望ましい。その代表例としては、オ
クタデンルエチレン尿素、N−メチロ−M高級脂肪酸ア
ミドなどをあげることができる。On the other hand, as the long-chain alkyl compound (b), one having an ethylene urea group or an N-methylol group is used in order to react with the copolymer described below. It is desirable that the long-chain acyl group in this compound has 16 to 24 carbon atoms in terms of the properties of the releasable treatment agent obtained and the physical properties of the releasable treatment sheet formed. Typical examples thereof include octadenylethylene urea and N-methylo-M higher fatty acid amide.
他方、本発明において主に前記長鎖アルキル化合物の捕
獲剤として用いる共重合体0としては、例えばアクリル
酸、メタクリル酸、クロトン酸などで代表される力Vホ
キシル基を有するエチレン性不飽和単量体などと、例え
ばメタクリル酸メチル、アクリル酸エチル、アクリM酸
ブチル、アクリV酸オクチル、酢酸ビニル、アクリロニ
トリv1スチレンなどで代表されるアクリV系、メタク
リル系、ビニルエステル系などのエチレン性不飽和単量
体のような、前記カルボキシル基を有する単量体とは別
種で、かつ、これと共重合可能な単量体とからなるもの
をあげることができる。On the other hand, in the present invention, the copolymer 0 mainly used as a trapping agent for the long-chain alkyl compound is an ethylenically unsaturated monomer having a V-phoxyl group represented by acrylic acid, methacrylic acid, crotonic acid, etc. and ethylenic unsaturated compounds such as acrylic V-based, methacrylic-based, vinyl ester-based, represented by methyl methacrylate, ethyl acrylate, butyl acrylic acid, octyl acrylic acid, vinyl acetate, acrylonitriv1 styrene, etc. Examples include monomers that are different from the monomer having a carboxyl group and that are copolymerizable with the monomer.
上記したように本発明においては水液系の剥離性処理剤
とすることが望ましいので、前記した各成分はそれぞれ
、水溶性vl+tエステM樹脂の水溶液、該長鎖アルキ
M化合物の水分散液、該共重合体の水分散液の形態で好
ましく用いられる。その該長鎖アルキM化合物の水分散
液の具体例としては、「オフテックスEMJ (商品名
:保土谷化学社製)、[ユニベヲンWAJ (商品名:
開成化学社製)、「パラジウム8PJ(商品名二大原バ
ヲジウム社製)などの市販品をあげることができる。As mentioned above, in the present invention, it is desirable to use an aqueous stripping treatment agent, so each of the above-mentioned components is an aqueous solution of water-soluble VL+T Esthe M resin, an aqueous dispersion of the long-chain alkyl M compound, The copolymer is preferably used in the form of an aqueous dispersion. Specific examples of the aqueous dispersion of the long-chain alkyl M compound include "Oftex EMJ (trade name: manufactured by Hodogaya Chemical Co., Ltd.), [Unibewon WAJ (trade name:
Commercially available products include Palladium 8PJ (trade name, manufactured by Ni-Ohara Bawodium Co., Ltd.) and Palladium 8PJ (trade name, manufactured by Ni-Ohara Baodium Co., Ltd.).
また、該共重合体の水分散液の例としては、力Vホキシ
ル基を有する単量体10重量部とこれと共重合可能な別
種の単量体40〜990重量部とを水、界面活性剤、重
合開始剤などの存在下に共重合させて得られる、力!レ
イキシル基含有単量体を1〜20重量%含む共重合体の
エマルジッンなどをあげることができる。なお、そのエ
マルジ璽ンには必要に応じポリビニ!レアルコールのよ
うな安定剤、ポリアクリル酸のような増粘剤などが用い
られていてもよい。In addition, as an example of an aqueous dispersion of the copolymer, 10 parts by weight of a monomer having a V-phoxyl group and 40 to 990 parts by weight of another type of monomer copolymerizable therewith are mixed in water, a surface-active Power obtained by copolymerization in the presence of agents, polymerization initiators, etc. Examples include emulsion, a copolymer containing 1 to 20% by weight of a Reixyl group-containing monomer. In addition, the emulsion seal can be made of polyvinyl vinyl if necessary! A stabilizer such as real alcohol, a thickener such as polyacrylic acid, etc. may be used.
本発明における剥離性処理剤は、(6)水溶性ポリエス
テル樹脂を100重量部、の)該長鎖アVキル化合物を
5〜100重量部、0該共重合体ヲ30〜300重量部
(いずれも固形分として)の割合で配合したものである
。The release treatment agent in the present invention includes (6) 100 parts by weight of a water-soluble polyester resin, 5 to 100 parts by weight of the long chain V-kyl compound, and 30 to 300 parts by weight of the copolymer (both (as solid content).
該長鎖アルキル化合物の配合比が5重量部未満であると
十分な剥離性を有する剥離性処理−が形成されないし、
他方、100重量部を超えると該共重体における力Vホ
キシル基と反応できない分が残存することとなる結果、
粘着剤等の接着力を低下させ念ジするなどして好ましく
ない。If the blending ratio of the long-chain alkyl compound is less than 5 parts by weight, a releasable treatment with sufficient releasability will not be formed.
On the other hand, if the amount exceeds 100 parts by weight, a portion that cannot react with the V-phoxyl groups in the copolymer will remain;
This is undesirable because it lowers the adhesive strength of adhesives and causes irritation.
一方、該共重合体の配合比が30重量部未満であるとカ
ルボキシル基不足となって該長鎖アルキル化合物の未反
応物が残存することとなるし、他方、300重量部を超
えると相対的に水溶性ポリエステル樹脂が不足すること
となって、形成される剥離性処理1が接着力不足となり
、ポリエステル系基材に対するものとしては不向きな本
のとなって好ましくない。On the other hand, if the blending ratio of the copolymer is less than 30 parts by weight, there will be a shortage of carboxyl groups and unreacted substances of the long-chain alkyl compound will remain; on the other hand, if the blending ratio exceeds 300 parts by weight, the As a result, the water-soluble polyester resin is insufficient, and the resulting releasable treatment 1 has insufficient adhesive strength, making it unsuitable for use on polyester base materials.
本発明における剥離性処理剤は、上記の各成分(A、B
及びC)をff!媒体を介して混合したものよりなって
いる。その液媒体の使用量は、得られる剥離性処理剤の
塗工性などの点で、固形分濃度が5〜50重量%となる
よう;に用いることが適当である。The releasable treatment agent in the present invention includes each of the above components (A, B
and C) ff! It consists of something mixed through a medium. The amount of the liquid medium to be used is preferably such that the solid content concentration is 5 to 50% by weight, from the viewpoint of coating properties of the resulting releasable treatment agent.
そして、上記の剥離性処理剤を例えば基材に塗布し、加
熱乾燥させることばより水溶性ポリエステル樹脂並びに
該長鎖アルキル化合物と該共重合体との反応生成物から
なる本発明の剥離性処理層が形成される。形成する剥離
性処理層の厚さは0.1〜6pfn、なかんず< 0.
1〜1.5amが適当であるが、これに限定されない。Then, the above-mentioned releasable treatment agent is applied to, for example, a base material, and the releasable treatment layer of the present invention is made of a water-soluble polyester resin and a reaction product of the long-chain alkyl compound and the copolymer. is formed. The thickness of the peelable treated layer to be formed is 0.1 to 6 pfn, especially <0.
1 to 1.5 am is suitable, but not limited thereto.
本発明によれば、水溶性ポリエステ/I/樹脂と特殊な
長鎖アルキM化合物と共重合体とを用いたので、剥離紙
や粘着テープなどの形成に用いられるポリエステIし系
基材に対しても接着力と剥離性とのバランス性に優れた
剥離性処理wを得ることができる。したがって、実用途
において剥離性処理層が基材より簡単に脱落することが
防止されたポリエステル系基材よりなる剥離紙や粘着テ
ープなどを得ることができる。According to the present invention, since a water-soluble polyester/I/resin, a special long-chain alkyl M compound, and a copolymer are used, it can be used for polyester I-based substrates used for forming release papers, adhesive tapes, etc. However, it is possible to obtain a releasable treatment w with an excellent balance between adhesive strength and releasability. Therefore, it is possible to obtain release paper, adhesive tape, etc. made of a polyester base material in which the releasable treated layer is prevented from easily falling off from the base material in practical use.
また、接着力と剥離性とのバランスが適宜にコントロー
ルされた剥離性処理剤を得ることができて、基材ないし
粘着剤等の性質に対応した剥離性処理@を形成すること
ができる。Further, it is possible to obtain a releasability treatment agent in which the balance between adhesive force and releasability is appropriately controlled, and it is possible to form a releasability treatment @ corresponding to the properties of the base material, adhesive, etc.
次に実施例をあげて本発明をさらに詳細に説明する。 Next, the present invention will be explained in more detail with reference to Examples.
参考例1
アクリル酸7重量部、メタクリル酸メチル20重量部、
アク+7 v酸エチ1v80重量部、水100重量部及
び界面活性剤としてノイゲンEA−120i3重量部、
ネオダンR51重量部(いずれも第一工業製薬社製)を
aoox容の四ツロフラスコに入れて40分間チッ素置
換したのちこれを65°Cにまで昇温させ、次いでこれ
に過硫酸アンモニウム0゜3重量部を加えて攪拌下に重
合させた。Reference example 1 7 parts by weight of acrylic acid, 20 parts by weight of methyl methacrylate,
Aku+7 V acid ethyl 1v 80 parts by weight, 100 parts by weight of water, and 3 parts by weight of Neugen EA-120i as a surfactant.
51 parts by weight of Neodan R (all manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) was placed in an aoox four-volume flask and replaced with nitrogen for 40 minutes, then heated to 65°C, and then 0.3 parts by weight of ammonium persulfate was added to it. 1 part was added and polymerized while stirring.
こうして7重合率98.2%、粘t5150cp(25
℃)、固形分濃度51.6重量%の共重合体エマルジョ
ンを得た。In this way, the polymerization rate of 7 was 98.2%, the viscosity was 5150 cp (25
℃), and a copolymer emulsion with a solid content concentration of 51.6% by weight was obtained.
参考例2
メタクリル酸17重量部、アクリル酸ブチ/l/75重
量部、アクリロニトリル14重量部、水100重量部、
ハイテノーtVN −17(界面活性剤;第−工業製薬
社all)8重量部及び過硫酸アンモニウム0.8重量
部を用い、参考例1と同様にして、重合率96.8%、
粘度180Cp(25°C)、固形分濃度50.5重量
%の共重合体エマVシースを得た。Reference Example 2 17 parts by weight of methacrylic acid, 75 parts by weight of butylene acrylic acid, 14 parts by weight of acrylonitrile, 100 parts by weight of water,
Using 8 parts by weight of HytenortVN-17 (surfactant; Dai-Kogyo Seiyaku Co., Ltd. all) and 0.8 parts by weight of ammonium persulfate, a polymerization rate of 96.8% was obtained in the same manner as in Reference Example 1.
A copolymer Emma V sheath with a viscosity of 180 Cp (25°C) and a solid content concentration of 50.5% by weight was obtained.
実施例1
水溶性ポリエステル樹脂(ガグセンE8−904)の2
5重量%水溶液100重量部、固形分25重量%のオク
タデシ〃エチレン尿素のエマルジョン(オフテックスE
M)60重量部、参考例1の共重合体エマルジッン10
0重量部を混合して得た剥離性処理剤を、ポリエステル
フィルム5−tO(東し社製、厚さ25μm)に塗工し
、140°Cで2分間加熱乾燥させて厚さ0.5μmの
剥離性処理−を有する該フィルムを得た。Example 1 Water-soluble polyester resin (Gagsen E8-904) 2
Emulsion of octadecyethylene urea containing 100 parts by weight of a 5% by weight aqueous solution and 25% by weight of solids (Oftex E)
M) 60 parts by weight, copolymer emulsion 10 of Reference Example 1
The release agent obtained by mixing 0 parts by weight was applied to a polyester film 5-tO (manufactured by Toshi Co., Ltd., thickness 25 μm), and dried by heating at 140° C. for 2 minutes to a thickness of 0.5 μm. The film was obtained which had a releasability treatment of .
次いで、得られた該ポリエステルフィルムについて下記
の方法によりその剥離力及び脱落性を調べた。結果を表
に示した。なお、表中の各成分の重量部は固形分(以下
同様)としての値である。Next, the peeling force and shedding property of the obtained polyester film were examined by the following method. The results are shown in the table. Note that the parts by weight of each component in the table are values as solid content (the same applies hereinafter).
剥離性処理1を設けたポリエステルフィルムの処fjj
A−側に、ポリエステル粘着テープ(A 81 B i
日東電気工業社製)を、1M1度25°C1湿度65%
の雰囲気中で荷重’1kg0ロールを用いて貼付け、こ
れを30分間放置したのち、20°C1引張速度311
0 try/分の条件で該フィルムをテンシロン引張試
験機(島津製作所社製)により引き剥しく180度剥#
>、その剥離力を調べた。Treatment of polyester film provided with releasability treatment 1fjj
Polyester adhesive tape (A 81 B i
(manufactured by Nitto Electric Industry Co., Ltd.), 1M, 1 degree, 25°C, 65% humidity.
It was pasted using a roll with a load of '1kg0 in an atmosphere of
The film was peeled off at 180 degrees using a Tensilon tensile tester (manufactured by Shimadzu Corporation) under the condition of 0 try/min.
>The peeling force was investigated.
ホljエステVフィルムに設けた剥離住処f!Al!!
の表面を親指により力強くこすって、剥れるか否かを調
べた。そして、剥れない場合t−0、簡単に剥ぎ取れた
場合を×として評価した。Separation housing f installed in Holj Esthetic V Film! Al! !
The surface of the film was rubbed forcefully with the thumb to see if it would peel off. The evaluation was rated as t-0 if it could not be peeled off, and the evaluation was rated as x if it could be easily peeled off.
実施例2〜4
表に示した組成からなる剥離性処理剤を実施例1と同様
にして調製し、その剥離性処理剤を形成してその評価を
行った。結果を表に示した。Examples 2 to 4 A releasable treatment agent having the composition shown in the table was prepared in the same manner as in Example 1, and the releasable treatment agent was formed and evaluated. The results are shown in the table.
なお、用いた原料の固形分濃度は次の値である。In addition, the solid content concentration of the raw materials used was the following value.
「ガプセンE8−2011J及び「ガグセンE8−90
5J:25重量%、「ユニペランWAJ及び[バヲジウ
ム8PJ:25重量%
比較例1
オフテックスEM60重量部、参考例1の共重合体エマ
Mジ冒ン100重量部を混合してなる剥離性処理剤を調
製し、実施例1と同様にしてその剥離性処理剤を形成し
てその評価を行った。結果を表に示した。"Gapsen E8-2011J and"Gapsen E8-90
5J: 25% by weight, Uniperan WAJ and Baodium 8PJ: 25% by weight, Comparative Example 1: 60 parts by weight of Oftex EM, and 100 parts by weight of the copolymer Emma M Difurin of Reference Example 1. was prepared, and its peelability treatment agent was formed and evaluated in the same manner as in Example 1. The results are shown in the table.
比較例2
オクテ、VクスEM61.9重量部、参考例2の共重合
体エマルジョン50重量部を用い、比較例1と同様にし
て剥離性処理剤を調製し、その剥離性処理層を形成して
その評価を行った。結果を表に示した。Comparative Example 2 A release treatment agent was prepared in the same manner as in Comparative Example 1 using 61.9 parts by weight of Octe, VxEM and 50 parts by weight of the copolymer emulsion of Reference Example 2, and a release treatment layer was formed. and evaluated it. The results are shown in the table.
表より、水溶性ポリエステ/L/樹脂を配合することに
よりポリエステル系基材への接着力(脱落性)が改善さ
れること、長鎖アルキル系化合物の配合割合を変えるこ
とにより剥離力をコントロールできること、本発明の剥
離性処理層は実用上十分な接着力と剥離性とのバランス
性を有していることがわかる。From the table, the adhesion to the polyester base material (shedding property) is improved by blending water-soluble polyester/L/resin, and the peeling force can be controlled by changing the blending ratio of the long-chain alkyl compound. It can be seen that the releasable treated layer of the present invention has a practically sufficient balance between adhesive strength and releasability.
Claims (1)
)エチレン尿素基又はN−メチロール基を有する長鎖ア
ルキル化合物5〜100重量部、(C)カルボキシル基
を有する単量体とこれとは別種の単量体との共重合体3
0〜300重量部及び(D)液媒体からなる剥離性処理
剤で形成されてなる剥離性処理層。 2、剥離性処理剤が水溶性ポリエステル樹脂の水溶液と
、長鎖アルキル化合物の水分散液と、共重合体の水分散
液との混合液からなる水液系のものである特許請求の範
囲第1項記載の処理層。 3、ポリエステル系基材に適用するためのものである特
許請求の範囲第1項記載の処理層。[Claims] 1. (A) 100 parts by weight of water-soluble polyester resin, (B
) 5 to 100 parts by weight of a long-chain alkyl compound having an ethylene urea group or an N-methylol group, (C) a copolymer of a monomer having a carboxyl group and a different type of monomer 3
A releasable treatment layer formed of a releasable treatment agent consisting of 0 to 300 parts by weight and (D) a liquid medium. 2. The release agent is an aqueous solution consisting of a mixture of an aqueous solution of a water-soluble polyester resin, an aqueous dispersion of a long-chain alkyl compound, and an aqueous dispersion of a copolymer. The treatment layer according to item 1. 3. The treatment layer according to claim 1, which is applied to a polyester base material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59247148A JPS61126191A (en) | 1984-11-22 | 1984-11-22 | Three-component releasable treatment layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59247148A JPS61126191A (en) | 1984-11-22 | 1984-11-22 | Three-component releasable treatment layer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61126191A true JPS61126191A (en) | 1986-06-13 |
Family
ID=17159145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59247148A Pending JPS61126191A (en) | 1984-11-22 | 1984-11-22 | Three-component releasable treatment layer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61126191A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5990238A (en) * | 1997-09-19 | 1999-11-23 | 3M Innovative Properties Company | Release coating for adhesive articles and method |
JP2009179719A (en) * | 2008-01-31 | 2009-08-13 | Kyowa Ltd | On-demand printable adhesive tape and printed adhesive tape roll |
-
1984
- 1984-11-22 JP JP59247148A patent/JPS61126191A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5990238A (en) * | 1997-09-19 | 1999-11-23 | 3M Innovative Properties Company | Release coating for adhesive articles and method |
JP2009179719A (en) * | 2008-01-31 | 2009-08-13 | Kyowa Ltd | On-demand printable adhesive tape and printed adhesive tape roll |
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