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JP3401110B2 - Surface protection film - Google Patents

Surface protection film

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Publication number
JP3401110B2
JP3401110B2 JP04827795A JP4827795A JP3401110B2 JP 3401110 B2 JP3401110 B2 JP 3401110B2 JP 04827795 A JP04827795 A JP 04827795A JP 4827795 A JP4827795 A JP 4827795A JP 3401110 B2 JP3401110 B2 JP 3401110B2
Authority
JP
Japan
Prior art keywords
protective film
surface protective
film
adhesive layer
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP04827795A
Other languages
Japanese (ja)
Other versions
JPH08245934A (en
Inventor
茂 小沼
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
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Filing date
Publication date
Application filed by Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP04827795A priority Critical patent/JP3401110B2/en
Publication of JPH08245934A publication Critical patent/JPH08245934A/en
Application granted granted Critical
Publication of JP3401110B2 publication Critical patent/JP3401110B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は表面保護フィルムに関す
る。 【0002】 【従来の技術】表面保護フィルムは、表面保護機能の良
否を支配するフィルム全体の物性もさることながら、接
着層の特性が被保護体の種類によっては重要となる。即
ち、被保護体の製造時に貼付けられた表面保護フィルム
は、その被保護体の運搬、加工、保管中の移動等の取扱
を受けるときに剥離することのないよう確実に接着され
ていなければならないが、被保護体の使用時には、表面
保護フィルムは被保護体の表面に糊残り等の汚染を与え
ることなく簡単に剥離できることが必要である。 【0003】ポリカーボネート板、アクリル樹脂板等の
合成樹脂板は、表面硬度が比較的小さく傷付き易いもの
であるので、製造時に表面保護フィルムが貼付けられ
る。この際、貼付けられる表面保護フィルムとしては、
数多く提案されているが、近年最も一般的に使用されて
いるのは、エチレン−酢酸ビニル共重合体もしくは直鎖
状低密度ポリエチレンからなる粘着層を有するものであ
る。 【0004】通常、合成樹脂板から表面保護フィルムを
簡単に剥離できるというときの両者の接着力は80g/
25mm幅以下、できれば50g/25mm幅以下であ
ることが必要とされている。しかし、合成樹脂板等の被
保護体表面に貼付けられた表面保護フィルムの接着力
は、経時的に増加(接着昂進)し、温度(特に100℃
以上の高温)、圧力、紫外線等の高エネルギー照射によ
ってその傾向は一層加速される。従って、被保護体表面
に貼付される当初の表面保護フィルムの接着力が適当で
あっても、経時により使用時には接着昂進しており、剥
離しにくくなっていたり、被保護体の表面に糊残り、曇
り等の汚染を与えたりすることが多々あるのである。 【0005】表面保護フィルムを貼付けたままで高温に
加熱して被保護体を加工する場合、保護フィルムが接着
昂進して剥離し難くなるので、これを抑えるために初期
接着力を低く設定しておくと、表面保護フィルム貼付時
や流通過程で、貼付性が悪かったり、自然に剥離したり
して、表面保護フィルムの機能を全うできない。このよ
うな理由から表面保護フィルムの初期接着力は5g/2
5mm幅以上、できれば10g/25mm幅以上にする
ことが必要とされている。 【0006】上記機能を満足する表面保護フィルムとし
て、例えば、特開平3−47886号公報に、粘着剤
に、密度0.900〜0.920g/cm3 の直鎖状低
密度ポリエチレンに、粘着付与剤として、水添テルペン
樹脂、テルペン樹脂、及びテルペンフェノール樹脂群か
ら選ばれたものを0.1〜5重量%添加したもので、耐
熱性、耐UV性に優れた表面保護フィルムが開示されて
いる。 【0007】しかし、上記公報記載の表面保護フィルム
に用いられている粘着付与剤は同公報に記載されている
ように高温加熱で接着力が昂進してしまうので初期接着
力を低く設定せねばならず貼付性が必ずしもよくない。 【0008】 【発明が解決しようとする課題】本発明は叙上の事実に
鑑みなされたものであって、その目的とするところは、
初期粘着性に優れ、加熱処理を施しても粘着力の昂進が
少なく、その他高温環境下に置かれても被保護体の表面
を汚染することの少ない優れた表面保護フィルムを提供
することにある。 【0009】 【課題を解決するための手段】本発明は、基材フィルム
の一面に、完全水添ロジンのペンタエリスリトールエス
テル樹脂及び/又は芳香族変成テルペン樹脂0.3〜4
重量%と密度0.918〜0.924g/cm3 の低密
度ポリエチレン99.7〜96重量%とからなる粘着層
が形成されてなる表面保護フィルムをその要旨とするも
のである。 【0010】本発明において使用される基材フィルム
は、特に限定されるものではないが、例えば、ポリエチ
レン、ポリプロピレン等のオレフィン系樹脂からなるフ
ィルムが好適に使用される。又、基材フィルムは、1層
のみであってもよいし、2層以上のものであってもよ
い。又、上記基材フィルムは、光安定剤、酸化防止剤、
紫外線吸収剤等の安定剤、シラン系の滑剤、沈降性硫酸
バリウム、タルク、炭酸カルシウム、マイカ、酸化チタ
ン等の充填剤及び着色剤等が添加されてもよい。 【0011】本発明における粘着層の主成分である低密
度ポリエチレンの密度が、0.918g/cm3 未満で
あると、表面保護フィルムを貼付けたままで被保護体を
加工する場合等の高温加熱された後、表面保護フィルム
を剥離すると、被保護体表面に糊残りや曇り等の汚染を
与え、0.924g/cm3 を超えると粘着層表面が粗
となり初期接着力を低下させる傾向にある。 【0012】本発明における低密度ポリエチレンの密度
は、JIS K 6760「ポリエチレンの試験方法」
の5.2比重及び密度に準拠して測定したものをいう。 【0013】本発明における粘着層のもう1つの成分で
ある粘着付与剤は、上記低密度ポリエチレンと相溶性が
よく、表面保護フィルムを貼付けたままで被保護体を加
工する場合等の加工追従性がよい完全水添ロジンのペン
タエリスリトールエステル樹脂及び/又は芳香族変成テ
ルペン樹脂である。 【0014】上記完全水添ロジンのペンタエリスリトー
ルエステル樹脂は、工業粘着テープ工業会出版「粘着ハ
ンドブック」第101頁に水添ロジンの主成分として列
挙されている一つ、テトラヒドロアビエチン酸のペンタ
エリスリトールエステルであって、市販品としては、理
科ハーキュレ社製、商品名「フォーラル105」等があ
る。 【0015】上記芳香族変成テルペン樹脂は、上記「粘
着ハンドブック」第105頁に記載されているように、
芳香族モノマーとテルペンモノマーの共重合によって得
られるものであって、市販品としては、ヤスハラケミカ
ル社製、商品名「TR−105」等がある。 【0016】上記完全水添ロジンのペンタエリスリトー
ルエステル樹脂及び芳香族変成テルペン樹脂は、上記低
密度ポリエチレンに各々単独で添加されてもよいし、両
者を併用してもよい。 【0017】上記粘着付与剤の添加量が0.3重量%未
満の場合、初期接着力及び加熱を伴う加工処理を施した
場合の接着力が低下し、4重量%を超えると、上記加工
処理後の接着力が高くなり、いずれも好ましくない。 【0018】本発明の表面保護フィルムの厚さは、被保
護体を傷、汚れ等から保護し得る機能を有するものであ
れば特に限定されるものではないが、通常、粘着層の厚
さは、10〜30μm、基材層の厚さは30〜70μ
m、全厚さで40〜100μm程度のものが好ましい。 【0019】本発明の表面保護フィルムは、基材フィル
ムと粘着層とを個別にT−ダイ法やインフレーション法
等の成形法によって所定の厚さに成形しておき、その
後、基材フィルムと粘着層とを熱ラミネーションによっ
て一体とする方法、基材フィルム上に押出ラミネーショ
ン法によって粘着層を設ける方法、又は、上記基材フィ
ルムと粘着層とを同時にT−ダイ法やインフレーション
法等の多層押出成形法によって所定の厚さに成形する方
法により得られる。 【0020】 【作用】本発明の樹脂板用表面保護フィルムは、基材フ
ィルムの一面に、芳香族変成テルペン樹脂及び/又は完
全水添ロジンのペンタエリスリトールエステル樹脂0.
3〜4重量%と密度0.918〜0.924g/cm3
の低密度ポリエチレン99.7〜96重量%とからなる
粘着層が形成されてなるものであるので、高温加熱時に
接着昂進せず、逆に高温加熱すると接着力が低下するの
で、初期接着力を高く設定でき、初期粘着性に優れ、加
熱処理を施しても粘着力の昂進が少なく、その他高温環
境下に置かれても被保護体の表面を汚染することが少な
い。 【0021】 【実施例】以下、本発明の実施例を具体的に説明する。 【0022】(実施例1)密度0.918g/cm3
低密度ポリエチレン(住友化学社製、商品名:L−70
5)99.7重量%と完全水添ロジンのペンタエリスリ
トールエステル樹脂(理科ハーキュレ社製、商品名:フ
ォーラル105)0.3重量%とからなる粘着層と高密
度ポリエチレン(旭化成社製、商品名:S−360、密
度0.960g/cm3 )からなる基材層をインフレー
ション法で共押出し、粘着層の厚さ20μm、基材層の
厚さ40μmの表面保護フィルムを作製した。 【0023】(実施例2)密度0.924g/cm3
低密度ポリエチレン(住友化学社製、商品名:CY44
3)96重量%と芳香族変成テルペン樹脂(ヤスハラケ
ミカル社製、商品名「TR−105」)4重量%とから
なる粘着層に変更したこと以外、実施例1と同様にして
粘着層の厚さ20μm、基材層の厚さ40μmの表面保
護フィルムを作製した。 【0024】(比較例1)低密度ポリエチレン99.8
重量%と完全水添ロジンのペンタエリスリトールエステ
ル樹脂0.2重量%とからなる粘着層に変更したこと以
外、実施例1と同様にして粘着層の厚さ20μm、基材
層の厚さ40μmの表面保護フィルムを作製した。 【0025】(比較例2)低密度ポリエチレン95重量
%と完全水添ロジンのペンタエリスリトールエステル樹
脂5重量%とからなる粘着層に変更したこと以外、実施
例1と同様にして粘着層の厚さ20μm、基材層の厚さ
40μmの表面保護フィルムを作製した。 【0026】(比較例3)密度0.910g/cm3
直鎖状低密度ポリエチレン(三井石油化学社製、商品
名:1020L)99重量%と水添テルペン樹脂(ヤス
ハラケミカル社製、商品名:クリアロンP125)1重
量%とからなる粘着層に変更したこと以外、実施例1と
同様にして粘着層の厚さ20μm、基材層の厚さ40μ
mの表面保護フィルムを作製した。 【0027】性能試験 以上の実施例及び比較例によって得られた表面保護フィ
ルムに対し、次の項目について、以下に示す試験方法で
測定した。試験結果を表1に示す。 【0028】1.初期接着力:表面保護フィルムを厚さ
2mmのアクリル板にラミネーターで貼付け、これを温
度23℃、湿度65%RHの環境下に30分放置した
後、剥離幅25mmで180度剥離試験により、初期接
着力を測定した。 【0029】2.接着昂進性評価:表面保護フィルムを
厚さ2mmのアクリル板にラミネーターで貼付け、熱風
循環式オーブン中で、120℃×1時間、150℃×3
0分間、180℃×10分間の3条件で加熱し、常温に
なるまで放冷した後、23℃で30分放置後、剥離幅2
5mmで180度剥離強度を測定し、接着昂進性を評価
した。 3.汚染性評価:前項の接着昂進性評価用の試料につい
て、表面保護フィルムを剥離し、アクリル板表面の糊残
り及び曇りの有無をUVライト下で目視により観察評価
した。その結果を表1に示す。 【0030】 【表1】【0031】表1から明らかな如く、本発明の実施例
1、2の各表面保護フィルムは、いづれも、アクリル樹
脂板に対して十分な初期粘着力を有し、上記各被保護体
の表面に表面保護フィルムを貼付した状態で加熱処理を
行っても、粘着力が上昇することがなく、却って低下
し、用済み後に被保護体の表面から容易に表面保護フィ
ルムを引き剥がすことができる。又、引き剥がした後
も、被保護体の表面にクモリや糊残り等の汚染がない。 【0032】これに対し、比較例1では、初期接着力及
び加熱処理後の接着力ともに低く、貼付性が悪く、且
つ、流通、加工等の過程で自然に剥離するおそれがあ
る。比較例2は初期接着力及び加熱処理後の接着力とも
に高く、剥離が難しい。又、比較例3は接着昂進が若干
みられ、被保護体表面に糊残り及び曇り等の汚染を与え
る。 【0033】 【発明の効果】本発明の表面保護フィルムは、叙上の如
く構成されているので、高温加熱時に接着昂進せず、逆
に高温加熱すると接着力が低下するので、初期接着力を
高く設定でき、初期粘着性に優れ、加熱処理を施しても
粘着力の昂進が少なく、その他高温環境下に置かれても
被保護体の表面を汚染することが少ない。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a surface protective film. 2. Description of the Related Art In a surface protective film, the properties of the adhesive layer are important depending on the type of the object to be protected, in addition to the physical properties of the entire film which governs the quality of the surface protective function. That is, the surface protection film attached at the time of manufacturing the protected object must be securely bonded so as not to be peeled off when the protected object is subjected to handling such as transportation, processing, and movement during storage. However, when the object to be protected is used, it is necessary that the surface protective film can be easily peeled off without causing contamination such as adhesive residue on the surface of the object to be protected. [0003] A synthetic resin plate such as a polycarbonate plate and an acrylic resin plate has a relatively small surface hardness and is easily damaged, and thus a surface protective film is adhered during production. At this time, as the surface protection film to be attached,
Although many proposals have been made, the one most commonly used in recent years has an adhesive layer made of an ethylene-vinyl acetate copolymer or a linear low-density polyethylene. Normally, when the surface protection film can be easily peeled off from the synthetic resin plate, the adhesive strength between them is 80 g /.
It is required that the width be 25 mm or less, preferably 50 g / 25 mm or less. However, the adhesive strength of the surface protective film attached to the surface of the object to be protected such as a synthetic resin plate increases with time (adhesion increases), and the temperature (particularly 100 ° C.)
The tendency is further accelerated by high energy irradiation such as high temperature, pressure, and ultraviolet rays. Therefore, even if the adhesive strength of the initial surface protection film attached to the surface of the protected object is appropriate, the adhesion has increased during use with time, and it has become difficult to peel off, or adhesive remains on the surface of the protected object. In many cases, it causes contamination such as cloudiness. When the object to be protected is processed by heating to a high temperature with the surface protective film adhered, the protective film increases in adhesion and becomes difficult to peel off. Therefore, in order to suppress this, the initial adhesive strength is set low. At the time of sticking the surface protective film or during the distribution process, the sticking property is poor or the film is naturally peeled off, and the function of the surface protective film cannot be fulfilled. For this reason, the initial adhesive strength of the surface protective film is 5 g / 2.
It is required that the width be 5 mm or more, preferably 10 g / 25 mm or more. As a surface protective film satisfying the above functions, for example, JP-A-3-47886 discloses that a pressure-sensitive adhesive is applied to a linear low-density polyethylene having a density of 0.900 to 0.920 g / cm 3. A surface protective film excellent in heat resistance and UV resistance is disclosed in which an agent selected from the group consisting of hydrogenated terpene resin, terpene resin and terpene phenol resin is added in an amount of 0.1 to 5% by weight. I have. However, the tackifier used in the surface protection film described in the above-mentioned publication increases the adhesion by heating at a high temperature as described in the publication, so that the initial adhesion must be set low. Is not always good. [0008] The present invention has been made in view of the above facts, and has as its object
An object of the present invention is to provide an excellent surface protective film having excellent initial adhesiveness, little increase in adhesive strength even when subjected to a heat treatment, and less contamination of the surface of a protected object even in a high-temperature environment. . According to the present invention, a pentaerythritol ester resin of completely hydrogenated rosin and / or an aromatic modified terpene resin 0.3 to 4 is coated on one surface of a substrate film.
The gist of the present invention is a surface protection film on which an adhesive layer comprising a low-density polyethylene having a density of 0.918 to 0.924 g / cm 3 and a low-density polyethylene of 99.7 to 96 weight% is formed. Although the substrate film used in the present invention is not particularly limited, for example, a film made of an olefin resin such as polyethylene or polypropylene is preferably used. Further, the base film may have only one layer, or may have two or more layers. Further, the base film is a light stabilizer, an antioxidant,
A stabilizer such as an ultraviolet absorber, a silane-based lubricant, a filler such as precipitated barium sulfate, talc, calcium carbonate, mica, and titanium oxide, a coloring agent, and the like may be added. When the density of the low-density polyethylene, which is the main component of the pressure-sensitive adhesive layer in the present invention, is less than 0.918 g / cm 3 , the material is heated to a high temperature, for example, when processing an object to be protected with the surface protective film attached. Then, when the surface protective film is peeled off, contamination such as adhesive residue and fogging is given to the surface of the protected object, and when it exceeds 0.924 g / cm 3 , the surface of the pressure-sensitive adhesive layer tends to be rough and the initial adhesive strength tends to be reduced. The density of the low-density polyethylene in the present invention is determined according to JIS K 6760 “Testing method for polyethylene”.
5.2 measured according to specific gravity and density. The tackifier, which is another component of the pressure-sensitive adhesive layer in the present invention, has good compatibility with the above low-density polyethylene, and has a good process-following property when processing a material to be protected while the surface protective film is adhered. Good fully hydrogenated rosin pentaerythritol ester resin and / or aromatic modified terpene resin. The pentaerythritol ester resin of completely hydrogenated rosin is one of the pentaerythritol ester of tetrahydroabietic acid listed as a main component of hydrogenated rosin on page 101 of "Adhesion Handbook" published by Industrial Adhesive Tape Industry Association. Commercial products include "Foral 105" (trade name, manufactured by Rika Hercule Co., Ltd.). [0015] The aromatic modified terpene resin is, as described in the “Adhesion Handbook”, page 105,
It is obtained by copolymerization of an aromatic monomer and a terpene monomer, and commercially available products include "TR-105" (trade name, manufactured by Yasuhara Chemical Co., Ltd.). The completely hydrogenated rosin pentaerythritol ester resin and the aromatic modified terpene resin may be added to the low-density polyethylene alone or in combination. When the amount of the tackifier is less than 0.3% by weight, the initial adhesive strength and the adhesive force when a processing involving heating is performed are reduced. Adhesion afterwards increases, and neither is preferable. The thickness of the surface protective film of the present invention is not particularly limited as long as it has a function of protecting the object to be protected from scratches, dirt and the like. , 10-30 μm, the thickness of the substrate layer is 30-70 μm
m, and those having a total thickness of about 40 to 100 μm are preferable. In the surface protective film of the present invention, the base film and the adhesive layer are individually formed to a predetermined thickness by a forming method such as a T-die method or an inflation method. A method in which the layers are integrated by thermal lamination, a method in which an adhesive layer is provided on a base film by an extrusion lamination method, or a method in which the base film and the adhesive layer are simultaneously subjected to multilayer extrusion such as a T-die method or an inflation method. It is obtained by a method of molding to a predetermined thickness by the method. The surface protective film for a resin plate of the present invention has a modified aromatic terpene resin and / or a completely hydrogenated rosin pentaerythritol ester resin on one surface of a substrate film.
3-4% by weight and density 0.918-0.924 g / cm 3
Of the low-density polyethylene of 99.7 to 96% by weight, the adhesion does not increase when heated at a high temperature, and the adhesion decreases when heated at a high temperature. It can be set high, has excellent initial adhesiveness, has little increase in adhesive strength even when subjected to heat treatment, and has little contamination of the surface of the protected object even when placed in a high-temperature environment. Hereinafter, embodiments of the present invention will be described in detail. Example 1 Low-density polyethylene having a density of 0.918 g / cm 3 (trade name: L-70, manufactured by Sumitomo Chemical Co., Ltd.)
5) An adhesive layer composed of 99.7% by weight and 0.3% by weight of a completely hydrogenated rosin pentaerythritol ester resin (manufactured by Rika Hercule, trade name: Foral 105) and high-density polyethylene (manufactured by Asahi Kasei Corporation, trade name) : S-360, density 0.960 g / cm 3 ), which was co-extruded by an inflation method to produce a surface protective film having a thickness of 20 μm for the adhesive layer and a thickness of 40 μm for the substrate layer. Example 2 Low-density polyethylene having a density of 0.924 g / cm 3 (trade name: CY44, manufactured by Sumitomo Chemical Co., Ltd.)
3) The thickness of the pressure-sensitive adhesive layer was changed in the same manner as in Example 1 except that the pressure-sensitive adhesive layer was changed to 96% by weight and 4% by weight of an aromatic modified terpene resin (trade name: "TR-105" manufactured by Yasuhara Chemical Co., Ltd.). A surface protection film having a thickness of 20 μm and a thickness of the substrate layer of 40 μm was prepared. Comparative Example 1 Low-density polyethylene 99.8
In the same manner as in Example 1, except that the pressure-sensitive adhesive layer was composed of 0.2% by weight of pentaerythritol ester resin of completely hydrogenated rosin and 20% by weight of the pressure-sensitive adhesive layer and 40 μm in thickness of the base material layer. A surface protection film was produced. Comparative Example 2 The thickness of the adhesive layer was changed in the same manner as in Example 1 except that the adhesive layer was composed of 95% by weight of low-density polyethylene and 5% by weight of a completely hydrogenated rosin pentaerythritol ester resin. A surface protection film having a thickness of 20 μm and a thickness of the substrate layer of 40 μm was prepared. Comparative Example 3 99% by weight of a linear low-density polyethylene having a density of 0.910 g / cm 3 (manufactured by Mitsui Petrochemical Co., trade name: 1020L) and a hydrogenated terpene resin (manufactured by Yashara Chemical Co., trade name: Clearon P125) The thickness of the adhesive layer was 20 μm and the thickness of the base material layer was 40 μ in the same manner as in Example 1, except that the adhesive layer was changed to 1% by weight.
m of the surface protective film was prepared. Performance Test The surface protection films obtained in the above Examples and Comparative Examples were measured for the following items by the following test methods. Table 1 shows the test results. 1. Initial adhesive strength: A surface protective film was stuck on an acrylic plate having a thickness of 2 mm with a laminator, and left in an environment of a temperature of 23 ° C. and a humidity of 65% RH for 30 minutes. The adhesion was measured. 2. Evaluation of adhesion enhancement: A surface protective film was stuck on an acrylic plate having a thickness of 2 mm with a laminator, and in a hot air circulating oven, 120 ° C. × 1 hour, 150 ° C. × 3.
After heating at 0 ° C for 3 minutes at 180 ° C for 10 minutes, the mixture was allowed to cool to room temperature, then left at 23 ° C for 30 minutes, and then peeled off width 2
180 degree peel strength was measured at 5 mm, and the adhesion enhancement property was evaluated. 3. Contamination evaluation: The surface protection film was peeled off from the sample for evaluation of adhesion enhancement described in the preceding paragraph, and the presence or absence of glue residue and fogging on the acrylic plate surface was visually observed and evaluated under UV light. Table 1 shows the results. [Table 1] As is clear from Table 1, each of the surface protective films of Examples 1 and 2 of the present invention has a sufficient initial adhesive force to the acrylic resin plate, and the surface of each of the above-mentioned protected objects. Even if the heat treatment is performed in a state where the surface protective film is adhered, the adhesive strength does not increase but rather decreases, and the surface protective film can be easily peeled off from the surface of the protected object after use. Further, even after peeling, there is no contamination such as cloud or glue residue on the surface of the protected object. On the other hand, in Comparative Example 1, both the initial adhesive strength and the adhesive strength after the heat treatment are low, the sticking property is poor, and there is a possibility that the adhesive will spontaneously peel off in the course of distribution, processing and the like. In Comparative Example 2, both the initial adhesive strength and the adhesive strength after the heat treatment were high, and peeling was difficult. In Comparative Example 3, the adhesion was slightly increased, and the surface of the protected object was contaminated with adhesive residue and fogging. Since the surface protective film of the present invention is constituted as described above, the adhesion does not increase when heated at a high temperature, and the adhesion decreases when heated at a high temperature. It can be set high, has excellent initial adhesiveness, has little increase in adhesive strength even when subjected to heat treatment, and has little contamination of the surface of the protected object even when placed in a high-temperature environment.

Claims (1)

(57)【特許請求の範囲】 【請求項1】 基材フィルムの一面に、完全水添ロジン
のペンタエリスリトールエステル樹脂及び/又は芳香族
変成テルペン樹脂0.3〜4重量%と密度0.918〜
0.924g/cm3 の低密度ポリエチレン99.7〜
96重量%とからなる粘着層が形成されてなる表面保護
フィルム。
(57) [Claim 1] 0.3 to 4% by weight of a fully hydrogenated rosin pentaerythritol ester resin and / or an aromatic modified terpene resin and a density of 0.918 on one surface of a base film. ~
0.924 g / cm 3 low density polyethylene 99.7-
A surface protective film on which an adhesive layer consisting of 96% by weight is formed.
JP04827795A 1995-03-08 1995-03-08 Surface protection film Expired - Fee Related JP3401110B2 (en)

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Publication number Priority date Publication date Assignee Title
JP3660747B2 (en) * 1995-11-01 2005-06-15 積水化学工業株式会社 Surface protection film for acrylic plates
WO2010104144A1 (en) * 2009-03-13 2010-09-16 荒川化学工業株式会社 Modifier for resins, adhesive compositions, and thermoplastic resin compositions
CN104136565B (en) * 2012-03-08 2016-06-22 荒川化学工业株式会社 Hot-melt adhesive composition

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