JPH09169960A - Tacky label or tape and production thereof - Google Patents

Tacky label or tape and production thereof

Info

Publication number
JPH09169960A
JPH09169960A JP34913795A JP34913795A JPH09169960A JP H09169960 A JPH09169960 A JP H09169960A JP 34913795 A JP34913795 A JP 34913795A JP 34913795 A JP34913795 A JP 34913795A JP H09169960 A JPH09169960 A JP H09169960A
Authority
JP
Japan
Prior art keywords
tape
platinum
sensitive adhesive
agent layer
pressure
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
JP34913795A
Other languages
Japanese (ja)
Other versions
JP3047803B2 (en
Inventor
Toshio Oba
敏夫 大庭
Shinji Irifune
真治 入船
Kenichi Isobe
憲一 磯部
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.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu 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 Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP7349137A priority Critical patent/JP3047803B2/en
Publication of JPH09169960A publication Critical patent/JPH09169960A/en
Application granted granted Critical
Publication of JP3047803B2 publication Critical patent/JP3047803B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

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

Abstract

PROBLEM TO BE SOLVED: To produce a tacky label or tape capable of carrying out the in-line coating even in the combination of an addition reactional curing type silicone composition with an acrylic tacky agent and provide a method for producing the tacky label or tape. SOLUTION: This tacky label or tape is obtained by successively laminating a mold release agent layer 2 comprising a cured film of an addition reactional curing type silicone composition and an acrylic tacky agent layer 3 containing 0.01-1wt.% platinum-based catalyst poisoning substance. The tacky label or tape has excellent peeling characteristics and is capable of carrying out the in-line coating and excellent in productivity.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、商品などに貼り付
けされる粘着ラベルや荷造り用などの粘着テープ及びそ
の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an adhesive label attached to a product or the like, an adhesive tape for packing, and a method for producing the same.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】従来、
紙、加工紙、プラスチックフィルムなどの基材と粘着剤
との接着、固着を防止することを目的として、基材面に
シリコーン組成物の皮膜を形成し、離型性を付与するこ
とが行われている。
2. Description of the Related Art
For the purpose of preventing adhesion and sticking of a pressure sensitive adhesive to a base material such as paper, processed paper or plastic film, a silicone composition film is formed on the surface of the base material to impart releasability. ing.

【0003】この場合、基材面にシリコーン皮膜を形成
する方法としては、白金系化合物を触媒として、脂肪
族不飽和基を含有するオルガノポリシロキサンとオルガ
ノハイドロジェンポリシロキサンとを付加反応させて離
型性皮膜を形成する方法、有機錫化合物などの有機酸
金属塩触媒を使用してオルガノポリシロキサンを縮合反
応させて離型性皮膜を形成する方法などが知られてい
る。これらの方法において使用するシリコーン組成物
は、いずれも加熱によって皮膜を形成させる熱キュアー
タイプと称されるものであり、その性状によってシリコ
ーンをトルエンなどの有機溶剤に溶解した溶剤タイプ、
水に分散させたエマルジョンタイプ、シリコーンのみか
らなる無溶剤タイプに分類される。また、粘着剤として
は(イ)溶剤型ゴム系、(ロ)溶剤型アクリル系、
(ハ)エマルジョン型アクリル系、(ニ)ホットメルト
型に分類されるが、の付加反応硬化型シリコーンとア
クリル系粘着剤(特に(ロ)の溶剤型)の組合せにおい
ては、シリコーン塗工と粘着剤加工を同一ラインで行う
インライン方式で粘着ラベルもしくは粘着テープを製造
すると、剥離力が極端に重く、場合によっては剥離不能
となることがあった。このため上記組合せにおいては、
シリコーン塗工後エージングし、粘着剤を塗工するオフ
−ライン方式が通常行われている。
In this case, as a method for forming a silicone film on the surface of a substrate, an organopolysiloxane containing an aliphatic unsaturated group and an organohydrogenpolysiloxane are subjected to an addition reaction by using a platinum compound as a catalyst and then separated. A method of forming a moldable film, a method of forming a mold-releasing film by subjecting an organopolysiloxane to a condensation reaction using an organic acid metal salt catalyst such as an organic tin compound, are known. Silicone compositions used in these methods are all called a heat cure type for forming a film by heating, a solvent type in which silicone is dissolved in an organic solvent such as toluene depending on its properties,
It is classified into an emulsion type dispersed in water and a solventless type consisting only of silicone. As the adhesive, (a) solvent type rubber type, (b) solvent type acrylic type,
(C) Emulsion type acrylic type, (d) hot melt type, but in combination of addition reaction curing type silicone and acrylic adhesive (particularly (b) solvent type), silicone coating and adhesion When an adhesive label or adhesive tape is manufactured by an in-line method in which the agent processing is performed on the same line, the peeling force is extremely heavy, and in some cases, the peeling may not be possible. Therefore, in the above combination,
An off-line method of aging after silicone coating and coating an adhesive is usually used.

【0004】しかし、この場合においても、シリコーン
のエージング条件(温度、時間、湿度)により剥離力が
変化するため、一定の品質の粘着ラベルもしくは粘着テ
ープを製造するには、剥離力が安定する1週間程度のエ
ージングが必要であった。
However, even in this case, since the peeling force changes depending on the aging conditions (temperature, time, humidity) of silicone, the peeling force is stable in order to manufacture an adhesive label or adhesive tape of a certain quality. Weekly aging was required.

【0005】本発明は、上記事情に鑑みなされたもの
で、付加反応硬化型シリコーン組成物とアクリル系粘着
剤の組合せにおいてもインライン塗工が可能な粘着ラベ
ル又はテープ及びその製造方法を提供することを目的と
する。
The present invention has been made in view of the above circumstances, and provides an adhesive label or tape capable of in-line coating even in the combination of an addition reaction-curable silicone composition and an acrylic adhesive, and a method for producing the same. With the goal.

【0006】[0006]

【課題を解決するための手段及び発明の実施の形態】本
発明者は、上記目的を達成するため鋭意検討を行った結
果、基材上にアルケニル基を含有するオルガノポリシロ
キサンと、オルガノハイドロジェンポリシロキサンと、
白金系触媒とを主成分とする付加反応硬化型シリコーン
組成物の硬化皮膜(離型剤層)を形成した後、この上に
白金系触媒被毒物質を0.01〜1%(重量%、以下同
じ)添加したアクリル系粘着剤を塗布した場合、剥離が
重くなることがなく、上記離型剤層の形成とアクリル系
粘着剤層の形成とを同一ライン(インライン)で行うこ
とができることを見い出した。
Means for Solving the Problems and Modes for Carrying Out the Invention As a result of intensive studies to achieve the above object, the present inventor has found that an organopolysiloxane containing an alkenyl group on a substrate and an organohydrogen Polysiloxane,
After forming a cured film (release agent layer) of an addition reaction curable silicone composition containing a platinum-based catalyst as a main component, 0.01 to 1% (wt%, platinum-based catalyst poisoning substance) of a platinum-based catalyst poisoning substance is formed thereon. The same shall apply hereinafter) When an added acrylic pressure-sensitive adhesive is applied, peeling does not become heavy, and it is possible to perform the formation of the release agent layer and the formation of the acrylic pressure-sensitive adhesive layer on the same line (in-line). I found it.

【0007】即ち、上記付加反応硬化型シリコーン組成
物に含まれる白金系触媒はオルガノポリシロキサンの硬
化反応に有効な触媒として作用するが、反応後も活性を
維持しており、シリコーン硬化皮膜中のSiH基とアク
リル系粘着剤中のアクリル基との付加反応触媒としても
作用するため、シリコーン硬化皮膜中のSiH基の残存
量が多いとアクリル系粘着剤では剥離が重くなる。これ
に対し、アクリル系粘着剤に白金系触媒被毒物質を添加
した場合、シリコーン硬化皮膜中の白金系触媒の触媒作
用が阻害され、シリコーン硬化皮膜中のSiH基とアク
リル系粘着剤中のアクリル基との付加反応が抑制され
て、離型剤層の形成とアクリル系粘着剤層の形成をイン
ラインで行っても、軽い剥離力が得られることを知見
し、本発明をなすに至ったものである。
That is, although the platinum-based catalyst contained in the addition reaction-curable silicone composition acts as an effective catalyst for the curing reaction of the organopolysiloxane, it retains its activity even after the reaction and the Since it also acts as an addition reaction catalyst between the SiH group and the acrylic group in the acrylic pressure-sensitive adhesive, if the residual amount of SiH group in the cured silicone film is large, the acrylic pressure-sensitive adhesive will be peeled off heavily. On the other hand, when the platinum-based catalyst poisoning substance is added to the acrylic adhesive, the catalytic action of the platinum-based catalyst in the silicone cured coating is inhibited, and the SiH group in the silicone cured coating and the acrylic adhesive in the acrylic adhesive are It was found that a light peeling force can be obtained even when the addition reaction with a group is suppressed and the release agent layer and the acrylic pressure-sensitive adhesive layer are formed in-line, and the present invention has been accomplished. Is.

【0008】なお、周囲温度ではヒドロシリル化反応を
抑制し、基材に薄膜塗工後加熱された場合は速やかにヒ
ドロシリル化反応を進行させるため、付加反応硬化型シ
リコーン組成物にはアセチレン化合物のような反応制御
剤が添加されているが、一般に沸点は200℃以下のも
のが使用されており、シリコーン硬化皮膜中の残存量は
少なく、かつ触媒を被毒させる作用が弱いため、SiH
基とアクリル系粘着剤との反応を防止する効果はほとん
どない。
In addition, since the hydrosilylation reaction is suppressed at ambient temperature and the hydrosilylation reaction proceeds rapidly when the substrate is heated after being applied as a thin film, the addition reaction-curable silicone composition is similar to an acetylene compound. Although a reaction control agent is added, the boiling point of 200 ° C or less is generally used, the residual amount in the cured silicone film is small, and the effect of poisoning the catalyst is weak.
There is almost no effect of preventing the reaction between the base and the acrylic adhesive.

【0009】従って、本発明は、(1)基材上の少なく
とも一面に、付加反応硬化型シリコーン組成物の硬化皮
膜からなる離型剤層及び白金系触媒被毒物質が0.01
〜1%添加されたアクリル系粘着剤層が順次積層されて
なることを特徴とする粘着ラベル又はテープ、(2)基
材上の少なくとも一面に、付加反応硬化型シリコーン組
成物の硬化皮膜からなる離型剤層を形成した後、これと
同一ラインで白金系触媒被毒物質が0.01〜1%添加
されたアクリル系粘着剤層を上記離型剤層上に形成する
ことを特徴とする粘着ラベル又はテープの製造方法を提
供する。
Therefore, according to the present invention, (1) a release agent layer composed of a cured film of an addition reaction curable silicone composition and a platinum-based catalyst poisoning substance of 0.01 are formed on at least one surface of a substrate.
A pressure-sensitive adhesive label or tape comprising an acrylic pressure-sensitive adhesive layer added in an amount of 1% to 1%, and (2) a cured film of an addition reaction-curable silicone composition on at least one surface of a substrate. After the release agent layer is formed, an acrylic pressure-sensitive adhesive layer containing 0.01 to 1% of a platinum catalyst poisoning substance is formed on the release agent layer in the same line as the release agent layer. A method for manufacturing an adhesive label or tape is provided.

【0010】以下、本発明につき更に詳しく説明する
と、本発明において、基材としては上質紙、グラシン
紙、ポリエチレンラミネート紙、クレーコート紙などの
紙基材やポリエチレン、ポリプロピレン、ポリエステル
などのフィルム基材が使用される。
The present invention will be described in more detail below. In the present invention, as the base material, a paper base material such as high-quality paper, glassine paper, polyethylene laminated paper, clay coated paper, or a film base material such as polyethylene, polypropylene or polyester. Is used.

【0011】本発明に使用される付加反応硬化型シリコ
ーン組成物は、1分子中に少なくとも2個のケイ素原子
に結合したアルケニル基を有するオルガノポリシロキサ
ンと、1分子中に少なくとも3個以上のケイ素原子に結
合した水素原子を有するオルガノハイドロジェンポリシ
ロキサンと、白金系触媒とを主成分とし、必要に応じて
ヒドロシリル化反応制御剤などを配合してなるもので、
この組成物としては公知のものを使用し得る。
The addition reaction curable silicone composition used in the present invention comprises an organopolysiloxane having an alkenyl group bonded to at least two silicon atoms in one molecule and at least three or more silicon atoms in one molecule. An organohydrogenpolysiloxane having a hydrogen atom bonded to an atom, a platinum-based catalyst as a main component, and a hydrosilylation reaction control agent and the like if necessary,
Known compositions can be used as this composition.

【0012】なお、アルケニル基を有するオルガノポリ
シロキサンにおいて、アルケニル基としてはビニル基、
アリル基、ヘキセニル基、ドデセニル基などが例示さ
れ、経済性から好ましいアルケニル基としてはビニル基
である。このアルケニル基は、オルガノポリシロキサン
中のケイ素原子に結合する全有機基に対して0.05〜
50モル%、特に0.2〜10モル%の割合で含有する
ことが好ましい。アルケニル基量が0.05モル%に満
たないと実質的な硬化速度が得られない場合があり、5
0モル%を超えると合成が困難になる上、剥離力も重く
なる。また、ケイ素原子に結合するアルケニル基以外の
有機基としては、例えば、メチル基、エチル基、プロピ
ル基等のアルキル基、フェニル基、トリル基等のアリー
ル基、あるいはこれらの炭素原子に結合した水素原子の
一部又は全部をハロゲン原子、シアノ基などで置換した
同種又は異種の置換又は非置換の一価炭化水素基などが
挙げられる。なお、ケイ素原子に結合するアルケニル基
以外の有機基は、全有機基に対して50モル%以上がメ
チル基であることが望ましい。
In the organopolysiloxane having an alkenyl group, the alkenyl group is a vinyl group,
Examples thereof include an allyl group, a hexenyl group, and a dodecenyl group, and the economically preferable alkenyl group is a vinyl group. This alkenyl group is from 0.05 to 0.05 with respect to all the organic groups bonded to the silicon atom in the organopolysiloxane.
The content is preferably 50 mol%, particularly 0.2 to 10 mol%. If the amount of alkenyl groups is less than 0.05 mol%, a substantial curing rate may not be obtained, and 5
If it exceeds 0 mol%, the synthesis becomes difficult and the peeling force becomes heavy. Examples of the organic group other than the alkenyl group bonded to the silicon atom include an alkyl group such as a methyl group, an ethyl group and a propyl group, an aryl group such as a phenyl group and a tolyl group, or a hydrogen bonded to these carbon atoms. Examples thereof include substituted or unsubstituted monovalent hydrocarbon groups of the same type or different types in which some or all of the atoms are substituted with halogen atoms, cyano groups and the like. It is desirable that 50 mol% or more of the organic groups other than the alkenyl group bonded to the silicon atom are methyl groups with respect to all the organic groups.

【0013】このオルガノポリシロキサンは直鎖状が望
ましいが、分岐状であってもよい。その末端のケイ素原
子に結合する置換基は、例えば、アルケニル基、アルキ
ル基、水酸基、アルコキシ基等のいずれの基であっても
よいが、アルケニル基が1個以上あることが好ましい。
The organopolysiloxane is preferably linear, but may be branched. The substituent bonded to the silicon atom at the terminal may be, for example, any group such as an alkenyl group, an alkyl group, a hydroxyl group, and an alkoxy group, but it is preferable that there is at least one alkenyl group.

【0014】なお、このオルガノポリシロキサンの粘度
は、通常25℃で100センチポイズ以上であることが
好ましい。
The viscosity of the organopolysiloxane is preferably 100 centipoise or higher at 25 ° C.

【0015】次に、オルガノハイドロジェンポリシロキ
サンは水素原子以外のケイ素原子に結合する有機基に特
に制限はなく、種々の有機基とすることができ、上記と
同様の有機基を挙げることができるが、全有機基の90
モル%以上はメチル基であることが望ましい。
Next, the organohydrogenpolysiloxane is not particularly limited in the organic groups bonded to silicon atoms other than hydrogen atoms, and various organic groups can be used, and the same organic groups as those mentioned above can be mentioned. However, 90 of all organic groups
It is desirable that the mol% or more is a methyl group.

【0016】このようなオルガノハイドロジェンポリシ
ロキサンとしては、具体的に(CH3)HSiO単位、
HSiO3/2単位、(CH32SiO単位、(CH33
SiO1/2単位からなるホモポリマー又はコポリマーな
どが例示され、これらは直鎖状、分岐状、環状のいずれ
であってもよい。
Specific examples of such an organohydrogenpolysiloxane include (CH 3 ) HSiO units,
HSiO 3/2 unit, (CH 3 ) 2 SiO unit, (CH 3 ) 3
Examples thereof include homopolymers or copolymers composed of SiO 1/2 units, which may be linear, branched or cyclic.

【0017】なお、このオルガノハイドロジェンポリシ
ロキサンの粘度は、通常25℃で10〜100センチポ
イズであることが好ましい。
The viscosity of the organohydrogenpolysiloxane is preferably 10 to 100 centipoise at 25 ° C.

【0018】オルガノハイドロジェンポリシロキサンの
配合量はアルケニル基含有オルガノポリシロキサンのア
ルケニル基量に応じて調整され、SiH基/アルケニル
基はモル比で1.2〜3.0であることが硬化性、基材
との密着性、剥離特性の面から望ましい。1.2未満で
は剥離性、皮膜形成性が損なわれ、3.0を超えると剥
離が重くなる。
The amount of the organohydrogenpolysiloxane blended is adjusted according to the amount of alkenyl groups in the alkenyl group-containing organopolysiloxane, and the SiH group / alkenyl group is in a molar ratio of 1.2 to 3.0. It is desirable in terms of adhesion to the substrate and peeling properties. If it is less than 1.2, the peeling property and film-forming property are impaired, and if it exceeds 3.0, the peeling becomes heavy.

【0019】更に、白金系触媒は付加反応を進めるため
の触媒であり、付加反応触媒として公知のものが使用で
きる。例えば塩化白金酸、塩化白金酸のアルコール溶液
やアルデヒド溶液、塩化白金酸と各種オレフィン、ビニ
ルシロキサンとの錯体などが挙げられ、アルケニル基含
有オルガノポリシロキサン100重量部に対して白金と
して0.001〜0.1重量部の範囲で使用される。
Further, the platinum-based catalyst is a catalyst for promoting the addition reaction, and a known addition reaction catalyst can be used. Examples thereof include chloroplatinic acid, alcoholic solutions of chloroplatinic acid, aldehyde solutions, complexes of chloroplatinic acid with various olefins and vinyl siloxanes, and 0.001 to 0.001 as platinum based on 100 parts by weight of alkenyl group-containing organopolysiloxane. Used in the range of 0.1 parts by weight.

【0020】一方、アクリル系粘着剤としては、従来か
ら粘着ラベル又はテープに用いられている公知のものを
使用することができ、例えばアクリル樹脂の有機溶剤溶
液である溶剤型アクリル系粘着剤や、アクリル樹脂の乳
化水分散体であるエマルジョン型アクリル系粘着剤など
が使用し得る。
On the other hand, as the acrylic pressure-sensitive adhesive, a known one conventionally used for pressure-sensitive adhesive labels or tapes can be used. For example, a solvent-type acrylic pressure-sensitive adhesive which is an organic solvent solution of acrylic resin, An emulsion type acrylic pressure-sensitive adhesive which is an emulsified water dispersion of an acrylic resin can be used.

【0021】本発明においては、このアクリル系粘着剤
に対し、白金系触媒被毒物質を添加する。この白金系触
媒被毒物質としては、トリフェニルホスフィン、ポリオ
キシエチレンアルキルエーテルのリン酸エステルなどの
リン原子含有化合物、ジブチル錫ジオクトエート、ジブ
チル錫ジアセテートなどの錫化合物、ジプロピルアミ
ン、ベンゾチアゾールなどのチッ素原子やイオウ原子を
有する化合物が例示される。なかでもリン系化合物が白
金系触媒に対する被毒作用が強いため優れている。ここ
で、白金系触媒被毒物質は粘着剤に添加され、この白金
系触媒被毒物質が添加された粘着剤は10〜50ミクロ
ンメーターの膜厚に塗工されるが、加熱後も白金系触媒
被毒物質が粘着剤層中に残存する必要があり、このため
白金系触媒被毒物質の沸点は常圧で200℃以上がよ
い。
In the present invention, a platinum catalyst poisoning substance is added to the acrylic pressure-sensitive adhesive. Examples of the platinum catalyst poisoning substance include phosphorus atom-containing compounds such as triphenylphosphine, phosphoric acid ester of polyoxyethylene alkyl ether, tin compounds such as dibutyltin dioctoate and dibutyltin diacetate, dipropylamine, benzothiazole, etc. Examples thereof include compounds having a nitrogen atom or a sulfur atom. Among them, phosphorus compounds are excellent because they have a strong poisoning effect on platinum catalysts. Here, the platinum-based catalyst poisoning substance is added to the pressure-sensitive adhesive, and the platinum-type catalyst poisoning substance-added pressure-sensitive adhesive is applied to a film thickness of 10 to 50 μm. It is necessary for the catalyst poisoning substance to remain in the pressure-sensitive adhesive layer. Therefore, the boiling point of the platinum-based catalyst poisoning substance is preferably 200 ° C. or higher under normal pressure.

【0022】粘着剤に添加する白金系触媒被毒物質の量
は粘着剤の固形分100重量部に対し、0.01〜1%
使用される。0.01%より少ないと、白金系触媒の働
きを防止する効果が少なく、1%より多いと粘着剤の特
性を損なうからである。なお、より好ましい範囲は0.
1〜0.5%である。
The amount of the platinum-based catalyst poisoning substance added to the adhesive is 0.01 to 1% with respect to 100 parts by weight of the solid content of the adhesive.
used. This is because if it is less than 0.01%, the effect of preventing the action of the platinum-based catalyst is small, and if it is more than 1%, the characteristics of the pressure-sensitive adhesive are impaired. A more preferable range is 0.
1 to 0.5%.

【0023】本発明の粘着ラベルもしくは粘着テープを
製造する場合、付加反応硬化型シリコーン組成物を紙、
プラスチックフィルム等の基材にドライで0.1〜3ミ
クロンメーターになるよう塗布し、加熱することにより
硬化皮膜を形成する。更にシリコーン硬化皮膜上に白金
系触媒被毒物質が添加されたアクリル系粘着剤を所定量
塗布乾燥後、粘着ラベルにおいては上紙を貼り付け、粘
着テープにおいてはそのまま巻き取ることにより、それ
ぞれ製造することが可能であり、図1,2に示すような
粘着テープ又は粘着ラベルを製造することができる。な
お、図中1は基材、2は離型剤層、3は粘着剤層、4は
表面紙である。
In the case of producing the pressure-sensitive adhesive label or tape of the present invention, the addition reaction-curable silicone composition is applied to paper,
A dry coating is applied to a substrate such as a plastic film so as to have a thickness of 0.1 to 3 μm, and the coating is heated to form a cured film. Further, a predetermined amount of an acrylic adhesive containing a platinum-based catalyst poisoning substance is applied on a cured silicone film, and after drying, a top paper is attached to the adhesive label and the adhesive tape is wound up as it is to produce each. It is possible to manufacture an adhesive tape or an adhesive label as shown in FIGS. In the figure, 1 is a base material, 2 is a release agent layer, 3 is an adhesive layer, and 4 is a surface paper.

【0024】ここで、シリコーン硬化皮膜を形成した直
後に同一ラインにおいて粘着剤を加工するいわゆるイン
ライン塗工は、エネルギー効率が高く、中間ストックが
不要であるなど生産上の利点が大きい。
Here, so-called in-line coating, in which the pressure-sensitive adhesive is processed in the same line immediately after forming the silicone cured film, has high energy efficiency and has great production advantages such as the need for intermediate stock.

【0025】[0025]

【発明の効果】以上説明したように、本発明の粘着ラベ
ルもしくは粘着テープは優れた剥離特性を有すると共
に、インライン塗工が可能で生産性にも優れる。
As described above, the pressure-sensitive adhesive label or pressure-sensitive adhesive tape of the present invention has excellent peeling properties, and in-line coating is also possible, resulting in excellent productivity.

【0026】[0026]

【実施例】以下、実施例及び比較例を示して本発明を具
体的に説明するが、本発明は下記実施例に制限されるも
のではない。なお、以下の例において部はいずれも重量
部であり、粘度は25℃の値である。
EXAMPLES The present invention will be described in detail below with reference to examples and comparative examples, but the present invention is not limited to the following examples. In the following examples, all parts are parts by weight, and the viscosity has a value of 25 ° C.

【0027】〔実施例1〕ポリエチレンラミネート紙基
材(1)のポリエチレンラミネート面に付加反応硬化型
シリコーン組成物KS847(信越化学工業(株)製)
100部をトルエン500部に溶解し、白金触媒Cat
−PL−50T(信越化学工業(株)製)1部を添加し
た剥離性塗工液をグラビアコーターを用いて、膜厚(ド
ライ)0.6ミクロンメーターになるよう塗工し、熱風
循環式乾燥器にて140℃で20秒間乾燥し、離型剤層
(2)を得た。
[Example 1] Addition reaction curable silicone composition KS847 (manufactured by Shin-Etsu Chemical Co., Ltd.) on the polyethylene laminated surface of the polyethylene laminated paper substrate (1).
Dissolve 100 parts in 500 parts of toluene, and use platinum catalyst Cat
-PL-50T (manufactured by Shin-Etsu Chemical Co., Ltd.) 1 part of a releasable coating liquid was applied using a gravure coater to a film thickness (dry) of 0.6 micrometer, and hot air circulation type The release agent layer (2) was obtained by drying at 140 ° C. for 20 seconds in a dryer.

【0028】この離型剤層(2)上に、溶剤型アクリル
系粘着剤BPS8170(東洋インキ製造(株)製)1
00部にベンゾチアゾール0.01部、0.1部、1部
を混合したものをそれぞれアプリケータを用いて膜厚2
5ミクロンメーターになるよう、硬化皮膜形成直後と2
5℃で24時間後に塗布し、100℃で3分間乾燥後、
粘着剤層(3)を設け、図1に示す粘着テープを得た。
On this release agent layer (2), a solvent-type acrylic pressure-sensitive adhesive BPS8170 (manufactured by Toyo Ink Mfg. Co., Ltd.) 1
A mixture of 00 parts with 0.01 parts, 0.1 parts and 1 part of benzothiazole was used to form a film having a film thickness of 2 using an applicator.
Immediately after forming the cured film and 2
After 24 hours at 5 ° C, apply and dry at 100 ° C for 3 minutes,
An adhesive layer (3) was provided to obtain the adhesive tape shown in FIG.

【0029】得られたテープを25℃で24時間熟成
後、180度方向へ0.3m/分の速度で剥離した時に
要する力を測定し、剥離力とした。また、剥離した粘着
面をステンレス板へ貼り付け、2kgのローラーで圧着
後、25℃で3時間放置し、180度方向へ0.3m/
分の速度で剥離した時に要する力を測定し、接着力とし
た。また、剥離した粘着面のタックをJ.DOW法に基
づき、停止するスチールボールの最大径で測定した。そ
れらの結果を表1に示す。
After the resulting tape was aged at 25 ° C. for 24 hours, the force required for peeling in the direction of 180 ° at a speed of 0.3 m / min was measured and used as the peeling force. Further, the peeled adhesive surface was attached to a stainless steel plate, pressure-bonded with a 2 kg roller, and left at 25 ° C. for 3 hours to give 180 m in a direction of 0.3 m /
The force required when peeling at a speed of minutes was measured and used as the adhesive force. Moreover, the tack of the peeled adhesive surface was measured by J. Based on the DOW method, the maximum diameter of the steel ball that stopped was measured. Table 1 shows the results.

【0030】〔実施例2〕グラシン紙基材(1)の片面
に付加反応硬化型シリコーン組成物KS847(信越化
学工業(株)製)100部をトルエン400部に溶解
し、白金触媒Cat−PL−50T(信越化学工業
(株)製)1部を添加した剥離性塗工液をグラビアコー
ターを用いて、膜厚(ドライ)0.9ミクロンメーター
になるよう塗工し、熱風循環式乾燥器にて120℃で3
0秒間乾燥し、離型剤層(2)を得た。
Example 2 On one side of the glassine paper base material (1), 100 parts of an addition reaction curable silicone composition KS847 (manufactured by Shin-Etsu Chemical Co., Ltd.) was dissolved in 400 parts of toluene, and a platinum catalyst Cat-PL was used. Using a gravure coater, a releasable coating solution containing 1 part of -50T (manufactured by Shin-Etsu Chemical Co., Ltd.) was applied to a film thickness (dry) of 0.9 micrometer, and a hot air circulation dryer was used. At 120 ° C for 3
It was dried for 0 seconds to obtain a release agent layer (2).

【0031】この離型剤層(2)上に、溶剤型アクリル
系粘着剤BPS8170(東洋インキ製造(株)製)1
00部にポリオキシエチレンアルキルエーテルのリン酸
エステル〔フォスファールRD−710(東邦化学工業
(株)製)〕0.1部を混合したものをアプリケータを
用いて膜厚25ミクロンメーターになるよう、硬化皮膜
形成直後と25℃で24時間後に塗布し、100℃で3
分間乾燥後、粘着剤層(3)を設け、その上に上質紙を
貼り付け、表面紙(4)とし、図2に示す粘着ラベルを
得た。
On this release agent layer (2), a solvent-type acrylic pressure-sensitive adhesive BPS8170 (manufactured by Toyo Ink Mfg. Co., Ltd.) 1
A mixture of 0.1 part of phosphoric acid ester of polyoxyethylene alkyl ether [Phospher RD-710 (manufactured by Toho Chemical Industry Co., Ltd.)] in 00 parts so that the film thickness becomes 25 μm using an applicator. Immediately after formation of the cured film and after 24 hours at 25 ° C, apply at 100 ° C for 3
After drying for a minute, a pressure-sensitive adhesive layer (3) was provided, and a high-quality paper was attached onto the pressure-sensitive adhesive layer to form a surface paper (4) to obtain the pressure-sensitive adhesive label shown in FIG.

【0032】得られたラベルを25℃で24時間熟成
後、実施例1と同様に剥離力、接着力、ボールタックを
測定した。結果を表2に示す。
After aging the obtained label at 25 ° C. for 24 hours, the peeling force, the adhesive force and the ball tack were measured in the same manner as in Example 1. Table 2 shows the results.

【0033】〔比較例1〕実施例1において溶剤型アク
リル系粘着剤BPS8170にベンゾチアゾールを添加
しないもので粘着テープを製造した。剥離力、接着力及
びボールタックの結果を表1に示す。
Comparative Example 1 A pressure-sensitive adhesive tape was manufactured by using the solvent-type acrylic pressure-sensitive adhesive BPS8170 in Example 1 without adding benzothiazole. The results of peeling force, adhesive force and ball tack are shown in Table 1.

【0034】〔比較例2〕実施例2において溶剤型アク
リル系粘着剤BPS8170にフォスファールRD−7
10を添加しないもので粘着ラベルを製造した。剥離
力、接着力及びボールタックの結果を表2に示す。
Comparative Example 2 In Example 2, solvent-type acrylic pressure-sensitive adhesive BPS8170 was added to Phosfar RD-7.
An adhesive label was produced without adding 10. The results of peeling force, adhesive force, and ball tack are shown in Table 2.

【0035】[0035]

【表1】 [Table 1]

【0036】[0036]

【表2】 [Table 2]

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の粘着テープの一例を示す断面図であ
る。
FIG. 1 is a cross-sectional view showing an example of an adhesive tape of the present invention.

【図2】本発明の粘着ラベルの一例を示す断面図であ
る。
FIG. 2 is a cross-sectional view showing an example of the adhesive label of the present invention.

【符号の説明】[Explanation of symbols]

1 基材 2 離型剤層 3 粘着剤層 4 表面紙 1 Base Material 2 Release Agent Layer 3 Adhesive Layer 4 Surface Paper

───────────────────────────────────────────────────── フロントページの続き (72)発明者 磯部 憲一 群馬県碓氷郡松井田町大字人見1番地10 信越化学工業株式会社シリコーン電子材料 技術研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kenichi Isobe 1 Hitomi, Oita, Matsuida-cho, Usui-gun, Gunma 10 Shin-Etsu Chemical Co., Ltd. Silicone Electronic Materials Research Laboratory

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 基材上の少なくとも一面に、付加反応硬
化型シリコーン組成物の硬化皮膜からなる離型剤層及び
白金系触媒被毒物質が0.01〜1重量%添加されたア
クリル系粘着剤層が順次積層されてなることを特徴とす
る粘着ラベル又はテープ。
1. An acrylic adhesive in which a release agent layer comprising a cured film of an addition reaction curable silicone composition and 0.01 to 1% by weight of a platinum catalyst poisoning substance are added to at least one surface of a substrate. A pressure-sensitive adhesive label or tape comprising an agent layer sequentially laminated.
【請求項2】 白金系触媒被毒物質が沸点200℃以上
のものである請求項1記載の粘着ラベル又はテープ。
2. The adhesive label or tape according to claim 1, wherein the platinum-based catalyst poisoning substance has a boiling point of 200 ° C. or higher.
【請求項3】 基材上の少なくとも一面に、付加反応硬
化型シリコーン組成物の硬化皮膜からなる離型剤層を形
成した後、これと同一ラインで白金系触媒被毒物質が
0.01〜1重量%添加されたアクリル系粘着剤層を上
記離型剤層上に形成することを特徴とする粘着ラベル又
はテープの製造方法。
3. A release agent layer comprising a cured film of an addition reaction-curable silicone composition is formed on at least one surface of a substrate, and the platinum-based catalyst poisoning substance is added in an amount of 0.01 to 0.01 in the same line. A method for producing a pressure-sensitive adhesive label or tape, comprising forming an acrylic pressure-sensitive adhesive layer added at 1% by weight on the release agent layer.
JP7349137A 1995-12-20 1995-12-20 Adhesive label or tape and method for producing the same Expired - Fee Related JP3047803B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7349137A JP3047803B2 (en) 1995-12-20 1995-12-20 Adhesive label or tape and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7349137A JP3047803B2 (en) 1995-12-20 1995-12-20 Adhesive label or tape and method for producing the same

Publications (2)

Publication Number Publication Date
JPH09169960A true JPH09169960A (en) 1997-06-30
JP3047803B2 JP3047803B2 (en) 2000-06-05

Family

ID=18401749

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7349137A Expired - Fee Related JP3047803B2 (en) 1995-12-20 1995-12-20 Adhesive label or tape and method for producing the same

Country Status (1)

Country Link
JP (1) JP3047803B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009214331A (en) * 2008-03-07 2009-09-24 Mitsubishi Plastics Inc Release film
JP2009220462A (en) * 2008-03-18 2009-10-01 Mitsubishi Plastics Inc Mold release film
JP2009220463A (en) * 2008-03-18 2009-10-01 Mitsubishi Plastics Inc Mold release film
JP2009226737A (en) * 2008-03-24 2009-10-08 Mitsubishi Plastics Inc Mold release film
WO2009150045A1 (en) * 2008-06-10 2009-12-17 Tesa Se Method for producing release liners
US20110123797A1 (en) * 2006-07-25 2011-05-26 Meir Soria Laser printer systems, intermediate transfer members, primer layers for intermediate transfer members, and primer layer compositions
JP2011523970A (en) * 2008-06-10 2011-08-25 テーザ・ソシエタス・ヨーロピア Pressure sensitive adhesive with improved release performance

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110123797A1 (en) * 2006-07-25 2011-05-26 Meir Soria Laser printer systems, intermediate transfer members, primer layers for intermediate transfer members, and primer layer compositions
US10072181B2 (en) * 2006-07-25 2018-09-11 Hewlett-Packard Development Company, L.P. Laser printer systems, intermediate transfer members, primer layers for intermediate transfer members, and primer layer compositions
JP2009214331A (en) * 2008-03-07 2009-09-24 Mitsubishi Plastics Inc Release film
JP2009220462A (en) * 2008-03-18 2009-10-01 Mitsubishi Plastics Inc Mold release film
JP2009220463A (en) * 2008-03-18 2009-10-01 Mitsubishi Plastics Inc Mold release film
JP2009226737A (en) * 2008-03-24 2009-10-08 Mitsubishi Plastics Inc Mold release film
WO2009150045A1 (en) * 2008-06-10 2009-12-17 Tesa Se Method for producing release liners
CN102057002A (en) * 2008-06-10 2011-05-11 德莎欧洲公司 Method for producing release liners
US20110186219A1 (en) * 2008-06-10 2011-08-04 Tesa Se Method for producing release liners
JP2011523970A (en) * 2008-06-10 2011-08-25 テーザ・ソシエタス・ヨーロピア Pressure sensitive adhesive with improved release performance
TWI481690B (en) * 2008-06-10 2015-04-21 Tesa Se Adhesive material with improved take-off behavior
US9074110B2 (en) 2008-06-10 2015-07-07 Tesa Se Method for producing release liners

Also Published As

Publication number Publication date
JP3047803B2 (en) 2000-06-05

Similar Documents

Publication Publication Date Title
US4849491A (en) Curable organopolysiloxane composition
KR100304470B1 (en) Composition for improving peeling strength of silicon paper peeling coating and method of manufacturing laminate using the same
JP3198926B2 (en) Curable silicone release agent composition and release paper
JPH0475942B2 (en)
JPH0554848B2 (en)
JPH04339816A (en) Epoxy-functional siloxane resin copolymer as controlled release additive
JPH09278893A (en) Silicone-based release coating composition
EP0103639B1 (en) Vinyl gum cure accelerators for condensation-cure silicone
US5945475A (en) Silicone release coating compositions
JPH0420570A (en) Silicone rubber composition excellent in peelability
JP3024445B2 (en) Silicone composition for release agent and release paper
JPH05186695A (en) Curable organopolysiloxane composition
JPH09169960A (en) Tacky label or tape and production thereof
JP2965231B2 (en) Silicone composition for release paper
JPS6320871B2 (en)
JP2915778B2 (en) Silicone composition for release paper
JP2934118B2 (en) Exposure resistant release agent
JPH0619028B2 (en) Organopolysiloxane composition for release coating
JP2698509B2 (en) Organopolysiloxane composition for release paper
JPH01215857A (en) Organopolysiloxane composition for release paper
JP3290581B2 (en) Peelable silicone composition for silicone adhesive
JP2508898B2 (en) Release paper manufacturing method
JPH0672207B2 (en) Silicone composition for release paper
JP3048470B2 (en) Curable silicone composition for release paper
JP2743739B2 (en) Curable organopolysiloxane composition for release paper

Legal Events

Date Code Title Description
FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100324

Year of fee payment: 10

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100324

Year of fee payment: 10

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110324

Year of fee payment: 11

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110324

Year of fee payment: 11

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120324

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120324

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130324

Year of fee payment: 13

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140324

Year of fee payment: 14

LAPS Cancellation because of no payment of annual fees