JPH03182577A - Surface covering material - Google Patents

Surface covering material

Info

Publication number
JPH03182577A
JPH03182577A JP32439189A JP32439189A JPH03182577A JP H03182577 A JPH03182577 A JP H03182577A JP 32439189 A JP32439189 A JP 32439189A JP 32439189 A JP32439189 A JP 32439189A JP H03182577 A JPH03182577 A JP H03182577A
Authority
JP
Japan
Prior art keywords
adhesive
self
adhesive layer
base material
water
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
JP32439189A
Other languages
Japanese (ja)
Inventor
Seinosuke Horiki
堀木 清之助
Kuninori Ito
邦矩 伊藤
Nobuhiko Kinooka
宣彦 紀岡
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.)
Nagoya Oil Chemical Co Ltd
Original Assignee
Nagoya Oil 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 Nagoya Oil Chemical Co Ltd filed Critical Nagoya Oil Chemical Co Ltd
Priority to JP32439189A priority Critical patent/JPH03182577A/en
Publication of JPH03182577A publication Critical patent/JPH03182577A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To obtain a surface covering material which can prevent a self-adhesive layer from being separated from a base material and transferred to a surface of an object when it is used to stick to a surface of an object and then peeled by applying an emulsified self-adhesive having a water-soluble proteinaceous polymer incorporated therein to one side of a base material comprising a polyolefin and drying it to form a self-adhesive layer thereon. CONSTITUTION:This surface covering material is prepared by applying an emulsified self-adhesive having a water-soluble proteinaceous polymer incorporated therein to one side of a base material comprising a polyolefin and drying it to form a self-adhesive layer thereon. As the emulsified self-adhesive, a natural or synthetic rubber latex or synthetic resin emulsion which shows self- adhesiveness at ordinary temperature is used. Examples of the water-soluble proteinaceous polymer include glue, casein, and albumin. The amount of the water-soluble proteinaceous polymer to be incorporated into the self-adhesive is usually about 0.1-30wt.%.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はマスキング材、包装材等に用いられる表面被覆
材に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a surface coating material used for masking materials, packaging materials, etc.

〔発明の背景〕[Background of the invention]

この種のマスキング材、包装材等の表面被覆材は紙、プ
ラスチックシート等の基材の表面に粘着層を設けたもの
であり、マスキング対象、包装対象等の表面に該粘着層
を介して貼着され5表面処理や輸送等の後剥離されるも
のである。そして剥離の際には粘着層が基材から剥離し
て上記対象の表面に移行しないことが要求される。しか
しながら該基材がポリエチレンやポリプロピレン等のポ
リオレフィンのような粘着層との親和性の低いプラスチ
ックを材料としたり、表面処理中に高温に曝されたり長
期にわたる保管や輸送の後に粘着層の上記対象表面への
移行を防止することは極めて困難なものである。
This type of surface covering material such as masking materials and packaging materials is made by providing an adhesive layer on the surface of a base material such as paper or plastic sheet, and is pasted onto the surface of the masking object, packaging object, etc. via the adhesive layer. It is then peeled off after surface treatment, transportation, etc. During peeling, it is required that the adhesive layer does not peel off from the base material and transfer to the surface of the object. However, if the base material is made of plastic with low affinity for the adhesive layer, such as polyolefin such as polyethylene or polypropylene, or if the target surface of the adhesive layer is exposed to high temperatures during surface treatment or after long-term storage or transportation, It is extremely difficult to prevent this transition.

〔従来の技術〕[Conventional technology]

従来、このような対象表面への粘着層の移行を防止する
には、粘着層を微架橋構造にして凝集力を向上させたり
、離型剤を添加して離型性を付与したりする方法が行な
われていた。
Conventionally, methods to prevent such migration of the adhesive layer to the target surface include creating a slightly crosslinked structure in the adhesive layer to improve cohesive strength, or adding a release agent to impart release properties. was being carried out.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら粘着層を微架橋構造にする方法では架橋密
度の調節が極めて微妙であり、適正架橋密度より若干高
いと粘着性が極端に低下したり、逆に若干低いと凝集力
が向上せず対象表面への粘着層の移行が防止出来ないし
、Ill型剤を添加する方法では粘着性の低下をきたし
たり、耐熱性、耐候性が低下したりする。
However, in the method of making the adhesive layer into a slightly crosslinked structure, the adjustment of the crosslinking density is extremely delicate, and if the crosslinking density is slightly higher than the appropriate crosslinking density, the adhesiveness will be extremely reduced, and conversely, if it is slightly lower than the appropriate crosslinking density, the cohesive force will not improve and the target surface It is not possible to prevent the transfer of the adhesive layer to the adhesive layer, and the method of adding an Ill-type agent causes a decrease in adhesiveness, and a decrease in heat resistance and weather resistance.

特にポリエチレンやポリプロピレン等のポリオレフイン
を基材とする場合には微架橋構造を形成したり、離型剤
を添加したりする従来の方法では完全に粘着層の対象表
面への移行を防止することが出来ない。しかしポリオレ
フィンは耐溶剤性を有しかつ安価であり、マスキング材
の基材としては好ましい材料である。
In particular, when the base material is polyolefin such as polyethylene or polypropylene, conventional methods such as forming a slightly crosslinked structure or adding a release agent cannot completely prevent the adhesive layer from transferring to the target surface. Can not. However, polyolefin has solvent resistance and is inexpensive, making it a preferred material as a base material for masking materials.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は上記従来の課題を解決するための手段として、
粘着層に蛋白質系水溶性高分子を添加するものである。
The present invention, as a means for solving the above-mentioned conventional problems,
A protein-based water-soluble polymer is added to the adhesive layer.

本発明に用いる基材はポリエチレン、ポリプロピレン、
エチレン−プロピレン共重合体等のポリオレフィンを材
料とする。上記基材は被覆対象の表面形状に適合する形
状に成形されていてもよい。
The base material used in the present invention is polyethylene, polypropylene,
The material is polyolefin such as ethylene-propylene copolymer. The base material may be formed into a shape that matches the surface shape of the object to be coated.

上記ポリオレフィンのシートまたはポリオレフィンの発
泡体のシートには無機充填材が混合されてもよい、上記
ポリオレフィンのシートまたはポリオレフィンの発泡体
のシートに混合される無機充填材とは炭酸カルシウム、
タルク、ベントナイト、チタン白、カーボン黒、ベンガ
ラ、ガラス粉、セラミック粉、高炉スラグ、フライアッ
シュ等の無機質の粉末である。そして該無機充填材は通
常上記ポリオレフィンのシートまたはポリオレフィンの
発泡体のシートに5〜80重量%望ましくは10〜60
重量%程度混合される。このようにポリオレフィンのシ
ートまたはポリオレフィンの発泡体のシートに無機充填
材を混合すると、マスキング材の強度や耐熱性が向上し
、またポリオレフィン材料やポリオレフィン発泡体材料
が無機充填材を添加した分節的されて、マスキング材の
材料費が低減する。また使用後のマスキング材を焼却す
る時にも燃焼エネルギーが無機充填材を添加した分減少
して焼却炉の損傷がそれだけ少なくなる。
An inorganic filler may be mixed in the polyolefin sheet or polyolefin foam sheet. The inorganic filler mixed in the polyolefin sheet or polyolefin foam sheet includes calcium carbonate,
Inorganic powders such as talc, bentonite, titanium white, carbon black, red iron, glass powder, ceramic powder, blast furnace slag, and fly ash. The inorganic filler is usually added to the polyolefin sheet or polyolefin foam sheet in an amount of 5 to 80% by weight, preferably 10 to 60% by weight.
About % by weight is mixed. Mixing an inorganic filler into a polyolefin sheet or a polyolefin foam sheet in this way improves the strength and heat resistance of the masking material, and also allows polyolefin materials or polyolefin foam materials to be mixed with segmented inorganic fillers. This reduces the cost of masking materials. Furthermore, when incinerating the masking material after use, the combustion energy is reduced by the amount of inorganic filler added, and damage to the incinerator is reduced accordingly.

本発明に用いる粘着剤は蛋白質系水溶性高分子を均一に
混合するためにエマルジョン型が採用されるが、このよ
うな粘着剤を例示すれば天然ゴム、スチレン−ブタジェ
ンゴム、スチレン−ブタジェンブロック共重合体、スチ
レン−イソプレンブロック共重合体、アクリロニトリル
−ブタジェンゴム、イソプレンゴム、クロロプレンゴム
、ブチルゴム、ポリイソブチレンゴム、ポリブテンゴム
The adhesive used in the present invention is of an emulsion type in order to uniformly mix the protein-based water-soluble polymer. Examples of such adhesives include natural rubber, styrene-butadiene rubber, and styrene-butadiene block. Polymers, styrene-isoprene block copolymers, acrylonitrile-butadiene rubber, isoprene rubber, chloroprene rubber, butyl rubber, polyisobutylene rubber, polybutene rubber.

グラフトゴム等の天然もしくは合成ゴムのラテックス、
アクリル酸エステル系樹脂、メタクリル酸エステル系樹
脂、酢酸ビニル系樹脂、プロピオン酸ビニル系樹脂、酢
酸ビニル−エチレン共重合体系樹脂、酢酸ビニル−マレ
イン酸共重合体系樹脂。
natural or synthetic rubber latex, such as grafted rubber;
Acrylic acid ester resin, methacrylic acid ester resin, vinyl acetate resin, vinyl propionate resin, vinyl acetate-ethylene copolymer resin, vinyl acetate-maleic acid copolymer resin.

スチレン系樹脂、塩化ビニル系樹脂、塩化ビニル−エチ
レン共重合体系樹脂、塩化ビニル−酢酸ビニル共重合体
系樹脂、塩化ビニリデン系樹脂、ポリビニルエーテル系
樹脂等の合成樹脂エマルジョンであって常温で粘着性を
示すものが用いられる。
Synthetic resin emulsions such as styrene resins, vinyl chloride resins, vinyl chloride-ethylene copolymer resins, vinyl chloride-vinyl acetate copolymer resins, vinylidene chloride resins, polyvinyl ether resins, etc., and are sticky at room temperature. The one shown is used.

上記合成ゴムラテックスおよび合成樹脂エマルジョンは
二種以上混合されてもよく、その場合には混合物として
常温で粘着性を示す配合であればよく1個々のラテック
スもしくはエマルジョンが必ずしも常温で粘着性を示す
必要はない、更に上記ラテックスもしくはエマルジョン
にはジブチルフタレート、ヂオクチルフタレート、トリ
クレジルホスフェイト、テルペンダイマー等の可塑剤も
しくは軟化剤が添加されてもよく、この場合も可塑剤も
しくは軟化剤の配合物が常温で粘着性を示せばよく1個
々のラテックスもしくはエマルジョンが必ずしも常温で
粘着性を示す必要はない。
Two or more of the above synthetic rubber latexes and synthetic resin emulsions may be mixed, and in that case, it is sufficient that the mixture exhibits tackiness at room temperature.1 Each individual latex or emulsion does not necessarily need to show tackiness at room temperature. In addition, plasticizers or softeners such as dibutyl phthalate, dioctyl phthalate, tricresyl phosphate, terpene dimers, etc. may be added to the latex or emulsion; It is not necessary for each latex or emulsion to exhibit tackiness at room temperature, as long as it shows tackiness at room temperature.

更に本発明の粘着剤にはロジン、石油樹脂、クマロン樹
脂、ロジン誘導体、テルペン系樹脂、フェノール系樹脂
、アルキルフェノール系樹脂等の粘着付与剤、トルエン
、キシレン、酢酸エチル、酢酸n−ブチル、7メチルエ
チルケトン、メチルイソブチルケトン、セロソルブアセ
テート、n−ブチルセロソルブ、エチレングリコール、
ジエチレングリコール、プロピレングリコール、グリセ
リン、ポリエチレングリコール、ポリプロピレングリコ
ール等の有機溶剤もしくは湿潤剤、タルク、ベントナイ
ト、炭酸カルシウム等の充填剤等が添加されてもよい、
その他、顔料、染料や防カビ剤、防腐剤等を添加しても
よい。
Furthermore, the adhesive of the present invention includes tackifiers such as rosin, petroleum resin, coumaron resin, rosin derivative, terpene resin, phenol resin, alkylphenol resin, toluene, xylene, ethyl acetate, n-butyl acetate, 7-methyl ethyl ketone. , methyl isobutyl ketone, cellosolve acetate, n-butyl cellosolve, ethylene glycol,
Organic solvents or wetting agents such as diethylene glycol, propylene glycol, glycerin, polyethylene glycol, polypropylene glycol, fillers such as talc, bentonite, calcium carbonate, etc. may be added.
In addition, pigments, dyes, fungicides, preservatives, etc. may be added.

本発明に用いられる蛋白質系水溶性高分子とは、例えば
ニカワ、ゼラチン、カゼイン、アルブミン等である。
Examples of the protein-based water-soluble polymer used in the present invention include glue, gelatin, casein, and albumin.

上記粘着剤に対する上記蛋白質系水溶性高分子の添加量
は通常0.1〜30重量%(以下単に%とする)望まし
くは0.1〜20%である。上記蛋白質系水溶性高分子
の添加量が30%を越えると粘着性が低下する傾向にあ
るが、充分な粘着性を有する粘着剤においては蛋白質系
水溶性高分子の添加量が30%を越えても粘着性が低下
しない場合もあり、上記数値は本発明を限定するもので
はない、また上記蛋白質系水溶性高分子の添加量が0.
1%以下になると粘着層の対象物に対する移行を防止す
る効果が低下する。上記蛋白質系水溶性高分子は通常エ
マルジョン型粘着剤にあとから添加するが、該粘着剤エ
マルジョンの生成(乳化重合または樹脂等の乳化)のさ
い、あらかじめ水相に添加しておいてもよい、また上記
蛋白質系水溶性高分子は粉末等の固形状あるいは水溶液
等の溶液にして添加される。
The amount of the water-soluble protein polymer added to the adhesive is usually 0.1 to 30% by weight (hereinafter simply referred to as %), preferably 0.1 to 20%. If the amount of the above-mentioned water-soluble protein-based polymer added exceeds 30%, the tackiness tends to decrease, but for adhesives with sufficient tackiness, the amount of water-soluble protein-based polymer added exceeds 30%. In some cases, the adhesiveness may not decrease even if the amount of water-soluble protein-based polymer added is 0.
When the amount is less than 1%, the effect of preventing the adhesive layer from transferring to the object decreases. The above protein-based water-soluble polymer is usually added to the emulsion-type adhesive later, but it may be added to the aqueous phase in advance during the production of the adhesive emulsion (emulsion polymerization or emulsification of resin etc.). The water-soluble protein polymer may be added in a solid form such as a powder or in a solution such as an aqueous solution.

本発明の表面被覆材を製造するには上記基材の対象物当
接面に粘着剤エマルジョンに上記蛋白質系水溶性高分子
を添加混合した混合物を塗布し。
To manufacture the surface coating material of the present invention, a mixture of the adhesive emulsion and the above protein-based water-soluble polymer is applied to the object contacting surface of the base material.

所望なれば通常80℃以上で加熱乾燥あるいは常温乾燥
後に80℃以上に加熱することによって粘着層を形成せ
しめる。粘着層としては通常50〜300 g / m
l程度の重量で基材上に形成される。
If desired, an adhesive layer is formed by drying by heating at 80° C. or higher or by heating at 80° C. or higher after drying at room temperature. Adhesive layer is usually 50-300 g/m
It is formed on the base material with a weight of about 1.

上記基材の表面には粘着剤エマルジョン塗布に先立ち放
電処理、プライマー処理が施されてもよい。
The surface of the base material may be subjected to electrical discharge treatment or primer treatment prior to application of the adhesive emulsion.

〔作用〕[Effect]

本発明の作用は下記の通りである。 The effects of the present invention are as follows.

蛋白質系水溶性高分子は粘着剤に混合されて該粘着剤の
凝集性を向上せしめるとともに離型性を付与する。そし
て蛋白質系水溶性高分子は高温時にも軟化しにくいもの
である。
A protein-based water-soluble polymer is mixed into an adhesive to improve the cohesiveness of the adhesive and to impart mold releasability. Protein-based water-soluble polymers do not easily soften even at high temperatures.

〔発明の効果〕〔Effect of the invention〕

したがって本発明の表面被覆材はポリオレフィンを基材
として用いても対象物表面に貼着され、この状態で高温
に曝されたり、かつ長期間経過しても、該表面被覆材を
剥離する時、粘着層が基材から対象物表面に移行するこ
とがない、また高温時に粘着剤の軟化等による被覆材の
基材からのはがれが防止できる。また貼着時における対
象物の表面温度の高低にかトわらず、接着性良好で保存
時のはがれがなく、また該表面被覆材を剥離する時はが
れ易くかつ粘着層の基材から対象物表面への移行は見ら
れない。
Therefore, even if the surface coating material of the present invention is made of polyolefin as a base material, it will stick to the surface of the object, and even if it is exposed to high temperatures in this state and even after a long period of time, when the surface coating material is peeled off, The adhesive layer does not migrate from the base material to the surface of the object, and peeling of the coating material from the base material due to softening of the adhesive at high temperatures can be prevented. In addition, regardless of the surface temperature of the object when it is pasted, it has good adhesion and does not peel off during storage, and when the surface coating material is peeled off, it easily peels off from the base material of the adhesive layer to the surface of the object. No transition is seen.

〔実施例〕〔Example〕

実施例1 50%天然ゴムラテックス70重量部と50%テルペン
樹脂の乳化エマルジョン30重量部からなる粘着剤エマ
ルジョンに対し蛋白質系水溶性高分子を第1表に示す比
率で加えたものを板状のポリエチレンシートの片面に5
0g/rrfで塗布し乾燥して表面被覆材を作成した。
Example 1 A plate-shaped adhesive emulsion consisting of 70 parts by weight of 50% natural rubber latex and 30 parts by weight of an emulsion of 50% terpene resin was added with a protein-based water-soluble polymer at the ratio shown in Table 1. 5 on one side of the polyethylene sheet
A surface coating material was prepared by coating at 0 g/rrf and drying.

該表面被覆材の試験結果を第2表に示す。The test results for the surface coating material are shown in Table 2.

(単位:重釦匍 第 表 第2表 (1)接着力剥離強さ:塗装板に粘着剤塗布面を介して
表面被覆材を貼着し、1日後の20℃における180度
剥離強さを測定する。
(Units: Table 2 (1) Adhesive force and peel strength: A surface coating material is attached to a painted board through the adhesive coated surface, and the 180 degree peel strength at 20°C after 1 day is measured. Measure.

(2)粘着剤残存性:塗装板に粘着剤塗布面を介して表
面被覆材を貼着し、これを20℃に1日および30日放
置後剥離し塗装板への粘着剤の移行の有無を調べた。
(2) Adhesive persistence: A surface coating material is attached to a painted board through the adhesive-applied surface, and it is left at 20°C for 1 and 30 days, then peeled off and whether or not the adhesive has migrated to the painted board. I looked into it.

(3〉加熱時粘着剤残存性=(2)粘着剤残存性と同様
に塗装板に表面被覆材を貼着し、1日後に80℃で1時
間放置し80℃での塗装板への粘着剤の移行の有無を調
べた。
(3> Adhesive persistence when heated = (2) Similar to adhesive persistence, apply the surface coating material to the painted board, leave it for 1 hour at 80°C after 1 day, and stick to the painted board at 80°C. The presence or absence of migration of the agent was investigated.

Oなし Oわずかにあり Δ かなりあり X はとんどあり 実施例2 アクリル酸n−ブチル7o重量部と酢酸ビニル30重量
部のモノマー比率で作成した50%粘着エマルジョン1
00重量部に対し蛋白質系水溶性高分子を第3表に示す
比率で加えたものを板状のポリプロピレンシートの片面
に50 g / rrfで塗布し乾燥して表面被覆材を
作成した。該表面被覆材の試験結果を第4表に示す。
O No O Slightly present Δ Very present
00 parts by weight and a protein-based water-soluble polymer added in the ratio shown in Table 3 was coated on one side of a plate-shaped polypropylene sheet at 50 g/rrf and dried to prepare a surface coating material. The test results for the surface coating material are shown in Table 4.

(単位二重電制 第 表 第4表 (4)接着剥離強さニアルミ板に粘着剤塗布面を介して
表面被覆材を貼着し、1日後の20℃における180度
剥離強さを測定する。
(Unit Double Electricity Table 4 Table 4 (4) Adhesive Peel Strength Adhere the surface coating material to the aluminum plate through the adhesive coated surface, and measure the 180 degree peel strength at 20°C one day later. .

(5)粘着剤残存性ニアルミ板に粘着剤塗布面を介して
表面被覆材を貼着し、これを20℃に1日および30日
放置後剥離しアルミ板への粘着剤の移行の有無を調べた
(5) Adhesive Residue A surface coating material is attached to the aluminum plate through the adhesive-coated surface, and after being left at 20°C for 1 day and 30 days, it is peeled off to check whether or not the adhesive has migrated to the aluminum plate. Examined.

(6)加熱時粘着剤残存性:(5)粘着剤残存性と同様
に塗装板に表面被覆材を貼着し、1日後に80℃で1時
間放置し80℃でのアルミ板への粘着剤の移行の有無を
調べた。
(6) Adhesive persistence when heated: Similar to (5) Adhesive persistence, the surface coating material was attached to the painted board, and after one day it was left at 80℃ for 1 hour, and the adhesion to the aluminum plate at 80℃ The presence or absence of migration of the agent was investigated.

・ なし     0 わずかにあり 0 わずかにあり Δ かなりあり X はとんどあり 実施例3 アクリル酸エチル50重量部とメタクリル酸メチル50
重量部のモノマー比率で作成した50%粘着エマルジョ
ン90重量部に、60%口ジン乳化液10重量部を添加
して51%粘着剤エマルジョンを得た。この粘着剤エマ
ルジョン100重量部に対し蛋白質系水溶性高分子を第
5表に示す比率で加えたものを30重量%の炭酸カルシ
ウムを混合したポリプロピレンシートの片面に50g/
ボで塗布し乾燥して表面被覆材を作成した。該表面被覆
材の試験結果を第6表に示す。
・ None 0 Slightly 0 Slightly Δ Quite a bit X Almost always Example 3 50 parts by weight of ethyl acrylate and 50 parts by weight of methyl methacrylate
A 51% adhesive emulsion was obtained by adding 10 parts by weight of a 60% gin emulsion to 90 parts by weight of a 50% adhesive emulsion prepared with a monomer ratio of 1 part by weight. To 100 parts by weight of this adhesive emulsion, a protein-based water-soluble polymer was added in the ratio shown in Table 5, and 50g/g of this was added to one side of a polypropylene sheet mixed with 30% by weight of calcium carbonate.
A surface coating material was created by applying it with a spray bottle and drying it. The test results for the surface coating material are shown in Table 6.

(単位:重釦匍 第 表 第6表 (7)接着力剥離強さ:塗装板に粘着剤塗布面を介して
表面被覆材を貼着し、1日後の20℃における180度
剥離強さを測定する。
(Unit: Table 6 (7) Adhesive force Peel strength: The surface coating material is pasted on the painted board through the adhesive coated surface, and the 180 degree peel strength at 20°C after 1 day is measured. Measure.

(8)粘着剤残存性:塗装板に粘着剤塗布面を介して表
面被覆材を貼着し、これを20℃に1日および30日放
置後剥離し塗装板への粘着剤の移行の有無を調べた。
(8) Adhesive persistence: Affix the surface coating material to the painted board through the adhesive-applied surface, leave it at 20°C for 1 day and 30 days, then peel it off and check whether the adhesive has migrated to the painted board. I looked into it.

(9)加熱時粘着剤残存性=(8)粘着剤残存性と同様
に塗装板に表面被覆材を貼着し、1日後に80℃で1時
間放置し80℃での塗装板への粘着剤の移行の有無を調
べた。
(9) Adhesive persistence when heated = (8) Adhesion of the surface coating material to the painted board in the same way as for (8) Adhesive persistence, and after 1 day, left at 80°C for 1 hour, and the adhesion to the painted board at 80°C The presence or absence of migration of the agent was investigated.

Oなし Oわずかにあり Δ かなりあり × はとんどあり 実施例4 50%ブチルゴムラテックス100重量部に対しタルク
3重量部、ポリプロピレングリコール1重量部からなる
51.9%粘着剤エマルジョン100重量部に対し蛋白
質系水溶性高分子を第7表に示す比率で加えたものを実
施例3のポリプロピレンシートの片面に100g/rr
rで塗布し乾燥して表面被覆材を作成した。該表面被覆
材の試験結果を第8表に示す。
O No O Slightly present Δ Very much × Mostly present Example 4 100 parts by weight of a 51.9% adhesive emulsion consisting of 3 parts by weight of talc and 1 part by weight of polypropylene glycol to 100 parts by weight of 50% butyl rubber latex. On the other hand, a protein-based water-soluble polymer was added at the ratio shown in Table 7 to one side of the polypropylene sheet of Example 3 at a rate of 100 g/rr.
A surface coating material was prepared by coating with r and drying. The test results for the surface coating material are shown in Table 8.

(単位:重量制 第 表 第8表 (10)熱老化後詰着剤残存性:塗装板に粘着剤塗布面
を介して表面被覆材を貼着してこれを40℃で熱老化を
加え1日、1ケ月、3ケ月、6ケ月後剥離し塗装板への
粘着剤の移行の有無を調べた。
(Unit: Weight system Table 8 (10) Residuality of adhesive after heat aging: A surface coating material is attached to a painted board through the adhesive coated surface, and then heat aged at 40°C for 1 day. After 1 month, 3 months, and 6 months, the adhesive was peeled off and the presence or absence of transfer of the adhesive to the painted board was examined.

Oなし Oわずかにあり Δ かなりあり × はとんどありNo O O slightly Δ Quite a bit × is almost always

Claims (1)

【特許請求の範囲】[Claims] ポリオレフィンを材料とする基材の一表面に蛋白質系水
溶性高分子を添加したエマルジョン型粘着剤を塗布し乾
燥することによって粘着層を形成したことを特徴とする
表面被覆材
A surface coating material characterized in that an adhesive layer is formed by applying an emulsion type adhesive containing a protein-based water-soluble polymer to one surface of a base material made of polyolefin and drying it.
JP32439189A 1989-12-13 1989-12-13 Surface covering material Pending JPH03182577A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32439189A JPH03182577A (en) 1989-12-13 1989-12-13 Surface covering material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32439189A JPH03182577A (en) 1989-12-13 1989-12-13 Surface covering material

Publications (1)

Publication Number Publication Date
JPH03182577A true JPH03182577A (en) 1991-08-08

Family

ID=18165269

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32439189A Pending JPH03182577A (en) 1989-12-13 1989-12-13 Surface covering material

Country Status (1)

Country Link
JP (1) JPH03182577A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106118587A (en) * 2016-07-15 2016-11-16 启东市和洪农副产品专业合作社 A kind of natural plant collagen adhesive

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106118587A (en) * 2016-07-15 2016-11-16 启东市和洪农副产品专业合作社 A kind of natural plant collagen adhesive

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