JPH07179830A - Surface protection film - Google Patents
Surface protection filmInfo
- Publication number
- JPH07179830A JPH07179830A JP32846093A JP32846093A JPH07179830A JP H07179830 A JPH07179830 A JP H07179830A JP 32846093 A JP32846093 A JP 32846093A JP 32846093 A JP32846093 A JP 32846093A JP H07179830 A JPH07179830 A JP H07179830A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- base material
- block copolymer
- protective film
- sensitive adhesive
- 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
Links
- 239000010410 layer Substances 0.000 claims abstract description 65
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 21
- 239000000463 material Substances 0.000 claims abstract description 20
- 230000001681 protective effect Effects 0.000 claims abstract description 16
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 15
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 15
- 229920001400 block copolymer Polymers 0.000 claims abstract description 14
- -1 polypropylene Polymers 0.000 claims abstract description 9
- 229920001971 elastomer Polymers 0.000 claims abstract description 8
- 229920005989 resin Polymers 0.000 claims abstract description 8
- 239000011347 resin Substances 0.000 claims abstract description 8
- 229920001384 propylene homopolymer Polymers 0.000 claims abstract description 7
- 229920001155 polypropylene Polymers 0.000 claims abstract description 6
- 239000004743 Polypropylene Substances 0.000 claims abstract description 5
- 239000005060 rubber Substances 0.000 claims abstract description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 abstract description 6
- 239000010959 steel Substances 0.000 abstract description 6
- 229920003002 synthetic resin Polymers 0.000 abstract description 4
- 239000000057 synthetic resin Substances 0.000 abstract description 4
- 239000012790 adhesive layer Substances 0.000 abstract description 3
- 239000000758 substrate Substances 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000003851 corona treatment Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011120 plywood Substances 0.000 description 3
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005673 polypropylene based resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
Landscapes
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
(57)【要約】
【目的】 プライマー処理や背面処理を施すことなく、
再剥離性や巻き戻し性に優れた、合成樹脂板、化粧板、
塗装鋼板等の表面保護フィルムの提供。
【構成】 ポリプロピレン系樹脂よりなる基材層の片面
にゴム系粘着剤層が形成されてなる表面保護フィルムに
おいて、基材層がプロピレンホモポリマー層と、プロピ
レンブロックコポリマー層を含む2層以上の積層体であ
り、プロピレンブロックコポリマー層上に粘着剤層を形
成することを特徴とする表面保護フィルム。(57) [Summary] [Purpose] Without applying primer treatment or back treatment,
Synthetic resin plate, decorative plate, which has excellent removability and rewindability,
Providing surface protection films for painted steel sheets, etc. A surface protective film having a rubber-based pressure-sensitive adhesive layer formed on one surface of a base material layer made of polypropylene resin, wherein the base material layer is a laminate of two or more layers including a propylene homopolymer layer and a propylene block copolymer layer. A surface protective film, which is a body and has an adhesive layer formed on a propylene block copolymer layer.
Description
【0001】[0001]
【産業上の利用分野】本発明は、合成樹脂板、化粧合
板、塗装を施した鋼板等の汚染防止及び外傷防止の目的
に使用する表面保護フィルムに関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a surface protective film used for the purpose of preventing contamination and external damage of synthetic resin plates, decorative plywood, coated steel plates and the like.
【0002】[0002]
【従来の技術】従来より、合成樹脂板、化粧合板、塗装
を施した鋼板等の汚染や外傷を防止する為にポリエステ
ル樹脂、ポリ塩化ビニル樹脂、ポリエチレン樹脂等の熱
可塑性樹脂基材に、再剥離性を有するゴム系、アクリル
系等の粘着剤層を形成した積層体が使用されている。2. Description of the Related Art Conventionally, in order to prevent contamination and external damage of synthetic resin plates, decorative plywood, coated steel plates, etc., thermoplastic resins such as polyester resin, polyvinyl chloride resin, polyethylene resin, etc. A laminated body having a peelable rubber-based or acrylic-based pressure-sensitive adhesive layer is used.
【0003】[0003]
【発明が解決しようとする課題】上記のような熱可塑性
樹脂基材に再剥離性を有する粘着剤層を形成した積層体
では、基材層と粘着剤層との密着性(接着性)が重要と
なる。この密着性が良好でない場合は、再剥離する際、
粘着剤層が被着体側に残留するという問題が生じる。こ
れら問題点を解決する為に基材層表面にコロナ処理やプ
ライマー処理が行われているが、コロナ処理の場合、効
果が小さく、又プライマー処理の場合は、製造工程が増
え、経済的に不利である。DISCLOSURE OF INVENTION Problems to be Solved by the Invention In a laminate in which a releasable pressure-sensitive adhesive layer is formed on a thermoplastic resin substrate as described above, the adhesion (adhesiveness) between the substrate layer and the pressure-sensitive adhesive layer is It becomes important. If this adhesion is not good, when peeling again,
There is a problem that the adhesive layer remains on the adherend side. In order to solve these problems, corona treatment or primer treatment is performed on the surface of the base material layer, but in the case of corona treatment, the effect is small, and in the case of primer treatment, the manufacturing process increases and it is economically disadvantageous. Is.
【0004】また、逆に基材層と粘着剤層との密着性が
良好な場合、表面保護フィルムの保管状態である巻き状
態から巻き戻す際、粘着剤が隣接するフィルムの基材層
側に取られるという現象が生じやすい。これを防止する
ため、剥離紙を挿入したり、基材フィルムに背面処理す
ることが行われているが、操作が繁雑である。そこで、
プライマー処理や背面処理を必要としない表面保護フィ
ルムが望まれていた。On the contrary, when the adhesiveness between the base material layer and the pressure-sensitive adhesive layer is good, when the surface protective film is unwound from the wound state which is the storage state, the pressure-sensitive adhesive is applied to the base material layer side of the adjacent film. The phenomenon of being taken is easy to occur. In order to prevent this, a release paper is inserted or a back surface treatment is performed on the base film, but the operation is complicated. Therefore,
There has been a demand for a surface protective film that does not require primer treatment or back treatment.
【0005】[0005]
【課題を解決するための手段】本発明者等は、上記の課
題を克服すべく鋭意検討した結果、プライマー処理する
ことなく、基材樹脂層と粘着剤層との密着性が良好であ
り、かつ、剥離紙や背面処理を必要としない表面保護フ
ィルムを開発するに至った。しかして本発明の要旨とす
るところは、ポリプロピレン系樹脂よりなる基材層の片
面に、ゴム系粘着剤層が形成されてなる表面保護フィル
ムにおいて、基材層がプロピレンホモポリマー層とプロ
ピレンブロックコポリマー層を含む2層以上の積層体で
あり、プロピレンブロックコポリマー層上に粘着剤層を
形成することを特徴とする表面保護フィルムに存する。Means for Solving the Problems As a result of intensive studies to overcome the above-mentioned problems, the present inventors have found that the adhesion between the base resin layer and the pressure-sensitive adhesive layer is good without primer treatment. In addition, we have developed a surface protection film that does not require release paper or back treatment. Therefore, the gist of the present invention is that in a surface protective film having a rubber-based pressure-sensitive adhesive layer formed on one side of a base material layer made of a polypropylene-based resin, the base material layer is a propylene homopolymer layer and a propylene block copolymer. A surface protective film, which is a laminate of two or more layers including layers, wherein a pressure-sensitive adhesive layer is formed on the propylene block copolymer layer.
【0006】以下、本発明について詳述する。本発明に
おいてプロピレンホモポリマーとは、通常工業的に製造
されているアイソタクティックポリプロピレンをいい、
メルトフローレートが0.5〜10のものを使用する。
更に必要に応じポリエチレンを30重量%以内の割合で
添加した混合物としてもよい。The present invention will be described in detail below. In the present invention, propylene homopolymer refers to isotactic polypropylene that is usually produced industrially,
A melt flow rate of 0.5 to 10 is used.
Further, if necessary, polyethylene may be added in a ratio of within 30% by weight to prepare a mixture.
【0007】また、プロピレンブロックコポリマーと
は、プロピレンと一種以上の異なったモノマーをブロッ
ク共重合したものをいい、メルトフローレートが0.5
〜10のものを使用する。コモノマーとしてはエチレン
が好ましく、具体的には、プロピレンホモポリマーを重
合した後、エチレンを装入あるいは、プロピレン・エチ
レン混合ガスを装入して重合を続け、プロピレン・エチ
レンコポリマーを生成させ、必要に応じEPR(エチレ
ンプロピレンラバー)等のエラストマーを添加したブロ
ック共重合体を用いる。コポリマー全量に対して、装入
するコモノマー成分の量は1〜10重量%が、エラスト
マー成分の量は1〜20重量%が好ましく、また、コモ
ノマー成分とエラストマー成分の合計を1〜30重量%
とするのが好ましい。各成分が所定範囲外の場合、粘着
剤層との密着性が十分でない恐れがあり好ましくない。
更に、本発明のプロピレンブロックコポリマーに対し
て、ポリエチレンやエチレン・酢酸ビニル共重合体等を
20重量%以内の割合で添加した混合物としても良い。The propylene block copolymer is a block copolymer of propylene and one or more different monomers, and has a melt flow rate of 0.5.
Use 10 to 10. Ethylene is preferable as a comonomer, and specifically, after polymerizing a propylene homopolymer, ethylene is charged or a propylene / ethylene mixed gas is charged to continue the polymerization to produce a propylene / ethylene copolymer, which is required. Accordingly, a block copolymer to which an elastomer such as EPR (ethylene propylene rubber) is added is used. With respect to the total amount of the copolymer, the amount of the comonomer component to be charged is preferably 1 to 10% by weight, the amount of the elastomer component is preferably 1 to 20% by weight, and the total amount of the comonomer component and the elastomer component is 1 to 30% by weight.
Is preferred. If each component is out of the predetermined range, the adhesiveness to the pressure-sensitive adhesive layer may be insufficient, which is not preferable.
Further, it may be a mixture obtained by adding polyethylene, an ethylene / vinyl acetate copolymer or the like to the propylene block copolymer of the present invention at a ratio within 20% by weight.
【0008】基材層の層構成としては、プロピレンホモ
ポリマー層を基材外層、プロピレンブロックコポリマー
層を基材内層とする2層の積層体でも、ポリエチレン、
エチレン・酢酸ビニル共重合体、ポリプロピレン接着性
樹脂等のポリオレフィン系樹脂を基材中間層とする3層
以上の積層体でも良い。基材層の厚みは内容物、用途に
応じて適宜決定すればよいが、通常20〜300μm程
度とする。20μm以下では外傷に対する抵抗性に劣る
場合があり、300μm以上では、取り扱い性に劣る場
合がある。また、基材層積層体の各層の厚みは特に制限
はないが、製造上5μm以上とするのがよい。As for the layer structure of the base material layer, a two-layer laminate comprising a propylene homopolymer layer as an outer base material layer and a propylene block copolymer layer as an inner base material layer, polyethylene,
It may be a laminate of three or more layers in which a polyolefin resin such as an ethylene / vinyl acetate copolymer or a polypropylene adhesive resin is used as a substrate intermediate layer. The thickness of the base material layer may be appropriately determined depending on the content and the application, but is usually about 20 to 300 μm. If it is 20 μm or less, resistance to external damage may be poor, and if it is 300 μm or more, handleability may be poor. The thickness of each layer of the base layer laminate is not particularly limited, but is preferably 5 μm or more in terms of production.
【0009】本発明に用いるゴム系粘着剤としては、従
来既知のものを使用すればよいが、天然ゴム系、合成ゴ
ム系粘着剤があり、具体的には、ブチルゴム系、スチレ
ン・ブタジエンゴム系、スチレン・イソプレンゴム系等
の粘着剤があげられる。また、本発明の目的を損なわな
い範囲内で、基材層及び/又は粘着剤層に公知の酸化防
止剤、紫外線吸収剤、光安定剤、無機微粒子、滑剤等の
添加剤を配合することができる。As the rubber-based pressure-sensitive adhesive used in the present invention, conventionally known ones may be used, and there are natural rubber-based and synthetic rubber-based pressure-sensitive adhesives, specifically, butyl rubber-based and styrene-butadiene rubber-based pressure-sensitive adhesives. Adhesives such as styrene and isoprene rubber can be used. In addition, known additives such as antioxidants, ultraviolet absorbers, light stabilizers, inorganic fine particles, and lubricants may be added to the base material layer and / or the pressure-sensitive adhesive layer within a range that does not impair the object of the present invention. it can.
【0010】本発明の基材層は、従来公知の方法、例え
ば多層Tダイ及び多層インフレーション装置等の押出し
機によって成膜・製造される。製造時にコロナ処理を行
ってもよい。また、基材層に粘着剤層を形成するには、
粘着剤をトルエン等の可溶な溶剤に溶解させた塗布液を
リバースコート法等の通常の方法により基材上に塗布
し、乾燥すればよい。The substrate layer of the present invention is formed and manufactured by a conventionally known method, for example, an extruder such as a multilayer T die and a multilayer inflation device. Corona treatment may be performed during manufacturing. Further, in order to form the adhesive layer on the base material layer,
A coating solution prepared by dissolving the pressure-sensitive adhesive in a soluble solvent such as toluene may be coated on the substrate by a usual method such as a reverse coating method and dried.
【0011】[0011]
【実施例】以下、本発明を実施例に基づいて詳細に説明
するが、本発明はその要旨を超えない限り、以下の例に
限定されるものではない。EXAMPLES The present invention will be described in detail below based on examples, but the present invention is not limited to the following examples as long as the gist thereof is not exceeded.
【0012】実施例1 基材外層のプロピレンホモポリマー層として、アイソタ
クティックポリプロピレン(メルトフローレート0.
9)100重量部に酸化防止剤(チバガイギー社、IR
GANOX−1010)0.5重量部を添加してなる樹
脂を用い、また基材内層のプロピレンブロックコポリマ
ー層として、ポリエチレンコポリマーを5重量%、EP
Rを10重量%含むプロピレンブロックコポリマー(メ
ルトフローレート0.8)100重量部に酸化防止剤
(IRGANOX−1010)0.5重量部を添加して
なる樹脂を用いて、2層Tダイ法にて各々の厚さ25μ
m,フィルムの総厚み50μmになるように成膜し、こ
れにポリイソブチレン粘着剤(ドネックス社、LM−M
H−LC100重量部+エクソン化学社、ビスタネック
スLM50重量部)をトルエン溶剤に溶かし、リバース
コート法により乾燥後10μm厚になるように基材内層
に塗布し、乾燥し、表面保護フィルムを得た。Example 1 As a propylene homopolymer layer as an outer layer of a substrate, isotactic polypropylene (melt flow rate: 0.
9) 100 parts by weight of an antioxidant (Ciba Geigy, IR
GANOX-1010) 0.5 part by weight of a resin is used, and 5% by weight of polyethylene copolymer, EP is used as the propylene block copolymer layer of the inner layer of the substrate.
Using a resin obtained by adding 0.5 part by weight of an antioxidant (IRGANOX-1010) to 100 parts by weight of a propylene block copolymer (melt flow rate 0.8) containing 10% by weight of R, a two-layer T-die method is used. And each thickness is 25μ
m, the film is formed so that the total thickness of the film is 50 μm, and a polyisobutylene adhesive (LM-M, manufactured by Donex Co., Ltd.)
H-LC 100 parts by weight + Exxon Chemical Co., Vistanex LM 50 parts by weight) was dissolved in a toluene solvent and applied to the inner layer of the base material by a reverse coating method so as to have a thickness of 10 μm after drying, followed by drying to obtain a surface protective film. .
【0013】比較例1 基材層として、実施例1の基材外層と同様の樹脂を用
い、単層Tダイ法にて厚み50μmのフィルムとし、実
施例1と同様の方法で粘着剤層を形成し、表面保護フィ
ルムを得た。 比較例2 基材層として、実施例1の基材内層と同様の樹脂を用
い、単層Tダイ法にて厚み50μmのフィルムとし、実
施例1と同様の方法で粘着剤層を形成し、表面保護フィ
ルムを得た。 比較例3 基材層を、実施例1と同様の2層フィルムとし、アクリ
ル系粘着剤を乾燥後10μm厚になるように基材内層に
塗布し、表面保護フィルムを得た。Comparative Example 1 As the substrate layer, the same resin as the substrate outer layer of Example 1 was used, and a film having a thickness of 50 μm was formed by the single-layer T-die method, and the pressure-sensitive adhesive layer was formed in the same manner as in Example 1. It formed, and the surface protection film was obtained. Comparative Example 2 As the base material layer, the same resin as the base material inner layer of Example 1 was used to form a film having a thickness of 50 μm by the single-layer T-die method, and the pressure-sensitive adhesive layer was formed by the same method as in Example 1, A surface protection film was obtained. Comparative Example 3 A two-layer film similar to that used in Example 1 was used as the base material layer, and an acrylic pressure-sensitive adhesive was applied to the inner base material layer to a thickness of 10 μm after drying to obtain a surface protective film.
【0014】上記実施例および比較例で得た表面保護フ
ィルムについて、初期粘着力、再剥離性及び巻き戻し性
を評価し、結果を表−1に示した。なお、評価方法は以
下の通りである。 (1)初期粘着力 塗装鋼板(塗料;アクリル−メラミン樹脂)に、得られ
た表面保護フィルムを貼り付け、JIS K6854に
準じ180°剥離強度にて評価した。With respect to the surface protective films obtained in the above Examples and Comparative Examples, the initial adhesive strength, removability and rewindability were evaluated, and the results are shown in Table-1. The evaluation method is as follows. (1) Initial Adhesion Strength The obtained surface protection film was attached to a coated steel sheet (paint; acrylic-melamine resin) and evaluated by 180 ° peel strength according to JIS K6854.
【0015】(2)再剥離性 表面保護フィルムを塗装鋼板に貼り付け、70℃×10
時間の条件下に放置した後、フィルムを剥がし、その時
の再剥離性を評価した。評価基準は次の通りである。 ○・・・良好(粘着剤残りなし) △・・・わずかに粘着剤の残り有り ×・・・粘着剤残り大(2) Removability A surface protective film was attached to a coated steel sheet, and the temperature was 70 ° C. × 10.
After being left under the condition of time, the film was peeled off, and the removability at that time was evaluated. The evaluation criteria are as follows. ○: Good (no adhesive remaining) △: Slight adhesive remaining ×: Large adhesive remaining
【0016】(3)巻き戻し性 表面保護フィルムを巻き状態で50℃×7日間の条件下
に放置した後、約10m/min で巻戻し、そのときの粘
着剤の背面への取られ程度を評価した。評価基準は次の
通りである。 ○・・・良好(粘着剤の背面への取られなし) △・・・わずかに取られる ×・・・著しく取られる(3) Rewinding property The surface protective film is left in a wound state at 50 ° C. for 7 days and then rewound at about 10 m / min. evaluated. The evaluation criteria are as follows. ◯: Good (no pressure-sensitive adhesive was picked up on the back surface) △: Slightly picked up ×: Significantly picked up
【0017】[0017]
【発明の効果】本発明の表面保護フィルムは、プライマ
ー処理や背面処理することなく、再剥離性や巻き戻し性
に優れ、合成樹脂板、化粧合板、塗装鋼板等の表面保護
フィルムとして極めて有用である。The surface protective film of the present invention is excellent in removability and rewindability without any primer treatment or back surface treatment and is extremely useful as a surface protective film for synthetic resin plates, decorative plywood, coated steel plates and the like. is there.
【0018】[0018]
【表1】 [Table 1]
Claims (2)
片面にゴム系粘着剤層が形成されてなる表面保護フィル
ムにおいて、基材層がプロピレンホモポリマー層と、プ
ロピレンブロックコポリマー層を含む2層以上の積層体
であり、プロピレンブロックコポリマー層上に粘着剤層
を形成することを特徴とする表面保護フィルム。1. A surface protective film comprising a base material layer made of polypropylene resin and a rubber-based pressure-sensitive adhesive layer formed on one surface thereof, wherein the base material layer comprises two or more layers including a propylene homopolymer layer and a propylene block copolymer layer. And a pressure-sensitive adhesive layer formed on the propylene block copolymer layer.
ノマー成分としてエチレンを1〜10重量%含有する請
求項1記載の表面保護フィルム。2. The surface protective film according to claim 1, wherein the propylene block copolymer contains 1 to 10% by weight of ethylene as a comonomer component.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32846093A JPH07179830A (en) | 1993-12-24 | 1993-12-24 | Surface protection film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32846093A JPH07179830A (en) | 1993-12-24 | 1993-12-24 | Surface protection film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07179830A true JPH07179830A (en) | 1995-07-18 |
Family
ID=18210518
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP32846093A Pending JPH07179830A (en) | 1993-12-24 | 1993-12-24 | Surface protection film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07179830A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008032691A1 (en) * | 2006-09-13 | 2008-03-20 | Sekisui Chemical Co., Ltd. | Surface-protective film |
| JP2011111551A (en) * | 2009-11-27 | 2011-06-09 | Nitto Denko Corp | Coating film protective sheet |
| JP2011111552A (en) * | 2009-11-27 | 2011-06-09 | Nitto Denko Corp | Coating film protective sheet |
-
1993
- 1993-12-24 JP JP32846093A patent/JPH07179830A/en active Pending
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008032691A1 (en) * | 2006-09-13 | 2008-03-20 | Sekisui Chemical Co., Ltd. | Surface-protective film |
| JPWO2008032691A1 (en) * | 2006-09-13 | 2010-01-28 | 積水化学工業株式会社 | Surface protection film |
| JP2011111551A (en) * | 2009-11-27 | 2011-06-09 | Nitto Denko Corp | Coating film protective sheet |
| JP2011111552A (en) * | 2009-11-27 | 2011-06-09 | Nitto Denko Corp | Coating film protective sheet |
| US9382453B2 (en) | 2009-11-27 | 2016-07-05 | Nitto Denko Corporation | Paint film-protecting sheet |
| US9382454B2 (en) | 2009-11-27 | 2016-07-05 | Nitto Denko Corporation | Paint film-protecting sheet |
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