JPH0827445A - Surface-protecting film - Google Patents

Surface-protecting film

Info

Publication number
JPH0827445A
JPH0827445A JP16106694A JP16106694A JPH0827445A JP H0827445 A JPH0827445 A JP H0827445A JP 16106694 A JP16106694 A JP 16106694A JP 16106694 A JP16106694 A JP 16106694A JP H0827445 A JPH0827445 A JP H0827445A
Authority
JP
Japan
Prior art keywords
film
propylene
rubber component
weight
ethylene
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
JP16106694A
Other languages
Japanese (ja)
Other versions
JP3347884B2 (en
Inventor
Masahiko Hiragori
正彦 平郡
Yoshinori Watanabe
良範 渡辺
Tadashi Kono
忠 甲野
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
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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP16106694A priority Critical patent/JP3347884B2/en
Publication of JPH0827445A publication Critical patent/JPH0827445A/en
Application granted granted Critical
Publication of JP3347884B2 publication Critical patent/JP3347884B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To obtain a surface-protecting film using a polyolefin-based resin film as a substrate and suitably used for applying machining such as drawing. CONSTITUTION:The olefinic resin forming a substrate comprises a propylene- based copolymer copolymerized by a reactor blend method. The propylene-based copolymer contains 30-60wt.% of a rubber component composed of an ethylene- propylene component, and has >=20wt.% of ethylene content in the rubber component and 40-70% crystallinity, 0.885-0.915g/cm<3> density and <=5g MFR/10min.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、ステンレス板、アルミ
ニウム板、カラー鋼板、カラーアルミニウム板等の金属
板の加工時、運搬時或いは保管時に、これら板体の表面
にゴミが付着したり、傷が付いたりするのを防止する為
に使用する表面保護フィルムであって、被着体に貼着し
た状態で絞り加工等の機械加工を施す場合に用いて好適
な表面保護フィルムに関する。
BACKGROUND OF THE INVENTION The present invention relates to a metal plate such as a stainless steel plate, an aluminum plate, a colored steel plate or a colored aluminum plate, which is processed, transported or stored, and has dust or scratches on its surface. The present invention relates to a surface protective film which is used to prevent the occurrence of sticking, and is suitable for use when mechanical processing such as drawing is performed in a state of being adhered to an adherend.

【0002】[0002]

【従来の技術】従来、金属板等の機械加工に適した表面
保護フィルムとしては、これを被着体表面に仮着したま
まで機械加工を施すので、本来、表面保護フィルムに要
求される品質特性である仮着性と再剥離性に加えて、機
械加工性を具えていることが要求される。この機械加工
性を具えた素材として、既存のフィルムの中では、軟質
塩化ビニル樹脂製フィルムが最も適しているので、押出
成形により成形された軟質塩化ビニル樹脂製フィルムを
基材とし、その一面に粘着剤層を設けてこれを被着体に
貼着したり、或いは、ポリ塩化ビニルゾルを被着体に直
接塗布して乾燥皮膜を形成したりする方法が汎用されて
いる。
2. Description of the Related Art Conventionally, as a surface protective film suitable for machining a metal plate or the like, it is mechanically processed while it is temporarily attached to the surface of an adherend. It is required to have machinability in addition to the properties of temporary adhesion and removability. Of the existing films, the soft vinyl chloride resin film is the most suitable material with this machinability, so the soft vinyl chloride resin film formed by extrusion is used as the base material, and one side A method in which a pressure-sensitive adhesive layer is provided and adhered to an adherend, or a polyvinyl chloride sol is directly applied to the adherend to form a dry film is widely used.

【0003】しかしながら、軟質塩化ビニル樹脂製のフ
ィルムは、用済み後の廃棄焼却の際に有毒ガスを発生す
るので衛生上、公害上の問題があり、これを改善するた
めにオレフィン系樹脂フィルムの採用が検討されてき
た。
However, a film made of a soft vinyl chloride resin has a problem in hygiene and pollution since it emits a toxic gas when it is discarded by incineration after it is used. Hiring has been considered.

【0004】例えば、特開昭53−21239号公報に
は、エチレンに炭素数4以上のα−オレフィンを共重合
したコポリマーを基材フィルムの原材料として使用する
技術が開示されている。これは所謂線状低密度ポリエチ
レンであって、この共重合樹脂が具えた機械的強度と柔
軟性とを利用することを狙いとするものである。
For example, Japanese Patent Application Laid-Open No. 53-21239 discloses a technique of using a copolymer obtained by copolymerizing ethylene with an α-olefin having 4 or more carbon atoms as a raw material for a base film. This is so-called linear low-density polyethylene, and its purpose is to utilize the mechanical strength and flexibility of the copolymer resin.

【0005】一方、特公平1−14265号公報には、
ポリエチレンとポリプロピレンとのブレンド物から成形
したフィルムを基材として使用する技術が開示されてい
る。つまり、ポリエチレンの柔軟性とポリプロピレンの
優れた機械的強度とを兼備させることを狙いとするもの
である。
On the other hand, Japanese Patent Publication No. 14265/1989 discloses that
A technique of using a film formed from a blend of polyethylene and polypropylene as a substrate is disclosed. That is, the purpose is to combine the flexibility of polyethylene with the excellent mechanical strength of polypropylene.

【0006】[0006]

【発明が解決しようとする課題】ところが、上記オレフ
ィン系樹脂フィルムを基材とする表面保護フィルムの
内、基材がコポリマーからなるものは、共重合段階にお
いてα−オレフィンの含量を大きくすることは難しく、
得られるフィルムは過度の柔軟性を有するものであり、
一方、基材がブレンド物からなるものは、両方の樹脂を
所定の配合割合のもとで均一に混合することが技術上極
めて難しく、所望する機械的特性を具備したものが得ら
れないという問題があった。
However, among the surface protective films having the above-mentioned olefin resin film as a base material, those having a base material of a copolymer cannot increase the α-olefin content in the copolymerization stage. Difficult,
The resulting film has excessive flexibility,
On the other hand, when the base material is made of a blend, it is technically extremely difficult to uniformly mix both resins at a predetermined mixing ratio, and it is impossible to obtain a material having desired mechanical properties. was there.

【0007】本発明は、上述のような表面保護フィルム
が抱える諸問題を解決し、特に、絞り加工等の機械加工
を施すものに用いて好適であり、衛生上、公害上の問題
も発生しないものを提供することを目的としてなされた
ものである。
The present invention solves various problems of the above-mentioned surface protective film, and is particularly suitable for use in those subjected to mechanical processing such as drawing, and does not cause problems in hygiene and pollution. It was made for the purpose of providing things.

【0008】[0008]

【課題を解決するための手段】本発明の表面保護フィル
ムにおいては、基材を形成するオレフィン系樹脂は、リ
アクターブレンド法により共重合されたプロピレン系共
重合体である。ここで、リアクターブレンド法とは、重
合が1回で終了するのでなく、2段階以上の多段重合を
行うことにより、複数の種類のポリマーを連続して製造
することができる重合法であり、機械的な手法を用いて
異種類のポリマーからなる混合樹脂を得るところの、所
謂、通常のポリマーブレンド法とは全く異なる手法であ
って、分子レベルでのブレンドタイプの共重合樹脂を生
産する方法である。こうして得られた樹脂は、各成分が
微細に分散することにより、混合される各樹脂が具有す
るところの、性質の異なる各機械加工性を忠実に具現し
たものが得られる。具体的な製造方法としては、例え
ば、特開平3−205439号公報に記載された方法で
ある。
In the surface protective film of the present invention, the olefin resin forming the substrate is a propylene copolymer copolymerized by the reactor blending method. Here, the reactor blending method is a polymerization method in which a plurality of types of polymers can be continuously produced by performing multi-stage polymerization of two or more steps instead of completing the polymerization once. It is a completely different method from the so-called ordinary polymer blending method of obtaining a mixed resin composed of different kinds of polymers using a conventional method, and it is a method of producing a blend type copolymer resin at the molecular level. is there. By finely dispersing the components, the resin thus obtained faithfully embodies the machinability having different properties, which the mixed resins have. A specific manufacturing method is, for example, the method described in JP-A-3-205439.

【0009】本発明においては、プロピレン系共重合体
は、エチレン−プロピレン成分よりなるゴム成分(以
下、単にゴム成分という)が30〜60重量%であり、
該ゴム成分中のエチレン量が20重量%以上でなければ
ならない。ゴム成分が、30重量%に満たない場合は、
絞り加工時に切れが発生し易くなり,60重量%を超え
ると過度の柔軟性を帯びたものとなって、機械的強度が
全般的に不足し、機械加工性に乏しいものとなるからで
ある。また、ゴム成分中のエチレン量が、20重量%に
満たない場合は、硬くなって曲げ加工が難しくなり、冷
間加工追従性も悪く、絞り加工時に切れが発生する。
In the present invention, the propylene-based copolymer has a rubber component comprising an ethylene-propylene component (hereinafter simply referred to as a rubber component) in an amount of 30 to 60% by weight,
The amount of ethylene in the rubber component must be 20% by weight or more. If the rubber component is less than 30% by weight,
This is because breakage is likely to occur during the drawing process, and when it exceeds 60% by weight, it becomes excessively flexible and mechanical strength is generally insufficient, resulting in poor machinability. Further, when the amount of ethylene in the rubber component is less than 20% by weight, the rubber component becomes hard and the bending process becomes difficult, the cold-working followability is poor, and a break occurs during the drawing process.

【0010】また、本発明で用いられるプロピレン系共
重合体は、結晶化度が40〜60%であり、密度が0.
885〜0.915g/cm3 であり、MFRが5g/
10分以下でなければならない。
The propylene-based copolymer used in the present invention has a crystallinity of 40 to 60% and a density of 0.
885 to 0.915 g / cm 3 , and MFR is 5 g / cm 3.
Must be 10 minutes or less.

【0011】結晶化度が40%未満であると、基材の弾
性率が低下するため、初期引張強度が低下し、フィルム
成形時、フィルム貼り付け時、引き剥がし時に、延び過
ぎて成形性、作業性が悪くなり、逆に、結晶化度が60
%を超えると、硬くなって応力緩和性が乏しくなり、絞
り加工時に浮きが発生するからである。
When the crystallinity is less than 40%, the elastic modulus of the base material is lowered, so that the initial tensile strength is lowered, and the film is excessively extended at the time of film molding, film sticking and peeling, resulting in moldability, Workability deteriorates, and conversely, the crystallinity is 60
This is because if it exceeds%, the alloy becomes hard and the stress relaxation property becomes poor, and floating occurs during drawing.

【0012】密度が0.885g/cm3 未満であると
機械的特性が全般に低くなり、0.915g/cm3
超えると柔軟性に乏しくなって冷間加工追従性が悪くな
り、絞り加工時に切れが発生するからである。
[0012] Density mechanical properties decreases in general is less than 0.885g / cm 3, 0.915g / cm 3 cold working follow-up property is deteriorated becomes poor flexibility exceeds, drawing This is because a break sometimes occurs.

【0013】また、MFRが5g/10分を超えると、
機械的特性が全般に低くなり、曲げ加工時に切断された
り、剥離時に伸びたりして作業性が低下する。
If the MFR exceeds 5 g / 10 minutes,
The mechanical properties are generally low, and the workability is reduced due to cutting during bending and elongation during peeling.

【0014】前述の原料を用いて、本発明の表面保護フ
ィルムの基材を得る場合、その基材の厚みとしては、適
用される被着体の板厚によっても異なるが、通常30〜
100μmであり、また、絞り加工でよく使われる板厚
1mm以下の被着体の場合は、30〜70μm程度のも
のが好ましい。
When the base material for the surface protective film of the present invention is obtained from the above-mentioned raw materials, the thickness of the base material is usually 30 to 30 although it varies depending on the thickness of the adherend to be applied.
In the case of an adherend having a plate thickness of 1 mm or less, which is 100 μm and is often used in drawing, the thickness is preferably about 30 to 70 μm.

【0015】また、本発明の表面保護フィルムに使用す
る粘着剤としては、表面保護フィルムとしての機能を満
足し得るものであれば、特に、ゴム系、アクリル系何れ
であっても差し支えなく、粘着剤層の形成手段として
も、塗工法、共押出法の何れの方法も採用できる。ま
た、このようにして得られる粘着剤層の厚みは、通常3
〜50μmである。
The pressure-sensitive adhesive used in the surface protective film of the present invention may be either rubber-based or acrylic-based as long as it can fulfill the function of the surface-protective film. As a method for forming the agent layer, either a coating method or a coextrusion method can be adopted. The thickness of the pressure-sensitive adhesive layer thus obtained is usually 3
˜50 μm.

【0016】尚、表面保護フィルムの実用性を高めるた
めに、剥離剤を基材の背面に使用したり、柔軟な基材で
ある関係上表面が滑り難くなるので、片面もしくは両方
の表層部に別の樹脂層を積層したり、基材を形成する原
材料中に、本発明の狙いとする効果を損なわない範囲内
で、他の配合物、例えば低密度ポリエチレン(LDP
E)、直鎖状低密度ポリエチレン(LLDPE)、高密
度ポリエチレン(HDPE)ポリプロピレン等を50重
量%の範囲内で混合使用したり、顔料等の添加剤を使用
するのは任意であるが、ポリプロピレンをベースとする
材料を使用した方がフィルムの応力緩和性能へ与える影
響を少なくしながら、他のフィルム物性を改善しやすい
ので好ましい。また、前述のリアクターブレンド法によ
って所望の共重合体を得る場合、重合釜内で更に他の機
能を付与するために、他のα−オレフインを含めてもよ
い。
In order to enhance the practicality of the surface protection film, a release agent is used on the back surface of the base material, and the soft base material makes the surface less slippery. Other compounds such as low density polyethylene (LDP) may be added to a raw material for laminating another resin layer or forming a base material as long as the effect of the present invention is not impaired.
E), linear low-density polyethylene (LLDPE), high-density polyethylene (HDPE) polypropylene, etc. may be mixed and used within a range of 50% by weight, and additives such as pigments may be optionally used. It is preferable to use a material based on (1) because it is easy to improve other physical properties of the film while reducing the influence on the stress relaxation performance of the film. Further, when the desired copolymer is obtained by the above-mentioned reactor blending method, other α-olefin may be contained in order to impart other functions in the polymerization vessel.

【0017】[0017]

【作用】本発明の表面保護フィルムは、基材を形成する
ポリオレフィン系樹脂として、上記したとおりのものを
使用しているので、曲げ加工、打ち抜き加工、絞り加工
等の各種機械加工性を具えたものとなっている。
The surface protective film of the present invention uses the above-mentioned polyolefin resin as a base material and therefore has various machinability such as bending, punching and drawing. It has become a thing.

【0018】[0018]

【実施例】以下、本発明の実施例について詳細に説明す
る。
EXAMPLES Examples of the present invention will be described in detail below.

【0019】(実施例1)リアクターブレンド法により
共重合されたプロピレン系共重合体として、ハイモント
社製のKS−021P(商品名、ゴム成分量=45重量
%、ゴム成分中のエチレン量=20重量%以上、結晶化
度=48%、密度=0.892g/cm3、MFR=
0.8g/10分)を用いて、インフレーション法によ
り厚みが70μmのオレフィン系樹脂フィルムを成形
し、得られたフィルムの片面にコロナ放電処理を施した
後、粘着剤溶液(綜研化学社製、商品名AG105)を
乾燥厚みで5μmとなるように塗布し、乾燥して、表面
保護フィルムのサンプルを得た。
(Example 1) As a propylene-based copolymer copolymerized by the reactor blending method, KS-021P (trade name, rubber component amount = 45% by weight, ethylene amount in rubber component = 20) manufactured by Highmont Co., Ltd. % By weight, crystallinity = 48%, density = 0.892 g / cm 3 , MFR =
0.8 g / 10 min) was used to mold an olefinic resin film having a thickness of 70 μm by an inflation method, and one side of the obtained film was subjected to corona discharge treatment, and then an adhesive solution (manufactured by Soken Chemical Industry Co., Ltd., A product name AG105) was applied so as to have a dry thickness of 5 μm and dried to obtain a surface protection film sample.

【0020】(実施例2)実施例1と同じプロピレン系
共重合体と、ポリプロピレン〔三菱化成社製AG352
1(商品名)〕とを、重量比3:1の割合となるように
混合した混合樹脂(ゴム成分量=34重量%、エチレン
量=20重量%以上、結晶化度=53%、密度=0.8
93g/cm3 、MFR=2.8g/10分)を使用し
たこと以外は、実施例1と同様にして表面保護フィルム
のサンプルを得た。
(Example 2) The same propylene copolymer as in Example 1 and polypropylene [AG352 manufactured by Mitsubishi Kasei Co., Ltd.
1 (trade name)] in a weight ratio of 3: 1 (rubber component amount = 34 wt%, ethylene amount = 20 wt% or more, crystallinity = 53%, density = 0.8
A surface protection film sample was obtained in the same manner as in Example 1 except that 93 g / cm 3 and MFR = 2.8 g / 10 min) were used.

【0021】(実施例3)実施例1と同じプロピレン系
共重合体を中層形成用樹脂とし、ポリプロピレン〔三菱
化成社製AG3521(商品名)〕を内外層形成用樹脂
として、3層の共押出インフレーション法により、厚み
構成が10:50:10であって且つ合計厚みが70μ
mのオレフィン系樹脂フィルムを成形し、以下実施例1
と同様にして表面保護フィルムのサンプルを得た。
(Example 3) The same propylene-based copolymer as in Example 1 was used as the resin for forming the middle layer, and polypropylene [AG3521 (trade name) manufactured by Mitsubishi Kasei Co., Ltd.] was used as the resin for forming the inner and outer layers, and three layers were coextruded. By the inflation method, the thickness composition is 10:50:10 and the total thickness is 70 μm.
m of the olefin resin film was molded, and
A surface protection film sample was obtained in the same manner as in.

【0022】(比較例1)直鎖状超低密度ポリエチレン
〔三井石油化学工業社製ウルトゼックス3520(商品
名)〕と、ポリプロピレン〔三菱化成社製AG3521
(商品名)〕とを重量比率で3:1の割合となるように
混合した混合樹脂〔ゴム成分量=3重量%未満、エチレ
ン量=20重量%未満、結晶化度=68%、密度=0.
904g/cm3 、MFR=3.3g/10分〕を使用
したこと以外は、実施例1と同様にして表面保護フィル
ムのサンプルを得た。
(Comparative Example 1) Linear ultra-low density polyethylene [Ultzex 3520 (trade name) manufactured by Mitsui Petrochemical Industry Co., Ltd.] and polypropylene [AG3521 manufactured by Mitsubishi Kasei Co., Ltd.]
(Commercial name)] in a weight ratio of 3: 1 [rubber component amount = less than 3% by weight, ethylene amount = less than 20% by weight, crystallinity = 68%, density = 0.
904 g / cm 3 , MFR = 3.3 g / 10 min] was used, and a sample of the surface protective film was obtained in the same manner as in Example 1.

【0023】(比較例2)プロピレン系共重合体〔ハイ
モント社製KS−011P(商品名)、ゴム成分量=2
7重量%、エチレン量=20重量%以上、結晶化度=7
5%、密度=0.892g/cm3 、MFR=10.0
g/10分〕を使用したこと以外は、実施例1と同様に
して表面保護フィルムのサンプルを得た。
(Comparative Example 2) Propylene-based copolymer [KS-011P (trade name) manufactured by Highmont, amount of rubber component = 2]
7% by weight, ethylene amount = 20% by weight or more, crystallinity = 7
5%, density = 0.892 g / cm 3 , MFR = 10.0
g / 10 min], a surface protection film sample was obtained in the same manner as in Example 1.

【0024】(比較例3)プロピレン系共重合体〔ハイ
モント社製KS−051P(商品名)、ゴム成分量=5
0重量%、エチレン量=20重量%以上、結晶化度=3
6%、密度=0.890g/cm3 、MFR=0.8g
/10分〕を使用したこと以外は、実施例1と同様にし
て表面保護フィルムのサンプルを得た。
(Comparative Example 3) Propylene-based copolymer [KS-051P (trade name) manufactured by Highmont, amount of rubber component = 5)
0% by weight, ethylene amount = 20% by weight or more, crystallinity = 3
6%, density = 0.890 g / cm 3 , MFR = 0.8 g
/ 10 min] was used to obtain a surface protection film sample in the same manner as in Example 1.

【0025】(比較例4)プロピレン系共重合体〔ハイ
モント社製KS−021P(商品名)〕と、ポリプロピ
レン〔三菱化成社製AG3521(商品名)〕とを、重
量比率で1:3の割合となるように混合した混合樹脂
〔ゴム成分量=11重量%、エチレン量=20重量%以
上、結晶化度=64%、密度=0.899g/cm3
MFR=4.5g/10分)を使用したこと以外は、実
施例1と同様にして表面保護フィルムのサンプルを得
た。
(Comparative Example 4) A propylene-based copolymer [KS-021P (trade name) manufactured by Highmont Co.] and polypropylene [AG3521 (trade name) manufactured by Mitsubishi Kasei Co.] were mixed at a weight ratio of 1: 3. A mixed resin mixed so that [amount of rubber component = 11% by weight, amount of ethylene = 20% by weight or more, crystallinity = 64%, density = 0.899 g / cm 3 ,
A surface protective film sample was obtained in the same manner as in Example 1 except that MFR = 4.5 g / 10 min) was used.

【0026】(比較例5)プロピレン系共重合体〔ハイ
モント社製KS−021P(商品名)〕と、直鎖状低密
度ポリエチレン〔三井石油化学社製ウルトゼックス35
20L(商品名)〕とを、重量比率で1:3の割合とな
るように混合した混合樹脂〔ゴム成分量=11重量%、
エチレン量=20重量%以上、結晶化度=62%、密度
=0.923g/cm3 、MFR=3.2g/10分)
を使用したこと以外は、実施例1と同様にして表面保護
フィルムのサンプルを得た。
Comparative Example 5 A propylene-based copolymer [KS-021P (trade name) manufactured by Highmont Co.] and a linear low-density polyethylene [Ultox 35 manufactured by Mitsui Petrochemical Co., Ltd.]
20L (trade name)] in a weight ratio of 1: 3, mixed resin [rubber component amount = 11% by weight,
Ethylene amount = 20% by weight or more, crystallinity = 62%, density = 0.923 g / cm 3 , MFR = 3.2 g / 10 minutes)
A sample of the surface protection film was obtained in the same manner as in Example 1 except that was used.

【0027】上記各実施例及び比較例で得られた表面保
護フィルムのサンプルについて、曲げ加工、打ち抜き加
工、絞り加工の各機械加工を行って、その機械加工性に
ついて評価を行い、その結果を表1に示す。尚、表1で
は、併せて、フィルム形成用樹脂についての結晶化度、
密度、MFR、ゴム成分量、エチレン量等を表示した。
また、試験方法、評価については次の通りである。
The surface protection film samples obtained in each of the above Examples and Comparative Examples were subjected to bending, punching and drawing, and their machinability was evaluated, and the results are shown. Shown in 1. In addition, in Table 1, in addition, the crystallinity of the resin for forming a film,
The density, MFR, rubber component amount, ethylene amount, etc. are displayed.
The test method and evaluation are as follows.

【0028】曲げ加工性:各サンプルをステンレス板
(厚み0.6mm、#SUS430BA)に貼着し、プ
レス機により90°の曲げ加工を行い、加工後の曲げ部
近傍フィルムの切れ及び剥離後のステンレス板の状態を
目視により観察。評価は、曲げ部近傍フィルムの切れ及
び剥離後の金属板の状態が両方とも異常が認められない
場合を◎、一方に異常が認められた場合を△、両方に異
常が認められた場合を×とした。
Bending workability: Each sample was adhered to a stainless plate (thickness: 0.6 mm, # SUS430BA), bent at 90 ° by a press machine, and after cutting and peeling of the film in the vicinity of the bent part after processing. Visually observe the condition of the stainless steel plate. The evaluation was ◎ when no abnormality was observed in the state of the metal plate after cutting and peeling of the film in the vicinity of the bent portion, ⊙ when abnormality was observed in one, × when abnormality was observed in both And

【0029】打ち抜き加工性:各サンプルを上記と同じ
ステンレス板に貼着し、プレス機ににより20mm径の
丸孔を打ち抜き、打抜き後の切断面及び剥離後のステン
レス板の状態を目視により観察。評価は、切断面及び剥
離後の金属板の状態が両方とも異常が認められない場合
を◎、一方に異常が認められた場合を△、両方に異常が
認められた場合を×とした。
Punching workability: Each sample was attached to the same stainless steel plate as described above, a circular hole having a diameter of 20 mm was punched out by a pressing machine, and the cut surface after punching and the state of the stainless steel plate after peeling were visually observed. The evaluation was rated as ⊚ when no abnormalities were found in both the cut surface and the state of the metal plate after peeling, Δ when abnormalities were found in one, and X when abnormalities were found in both.

【0030】絞り加工性:各サンプルを上記と同じステ
ンレス板に貼着し、30mm径の円柱状に、深さ15m
mの絞り加工を行い、40℃の恒温室内に1日間放置
後、フィルムの浮き状態を目視により観察し、その後、
フィルムを剥離し、剥離したフィルムの切れの有無を観
察。評価は、フィルムの浮き状態については、浮きのな
いものを◎、浮きのあるものを×とし、フィルムの切れ
の有無については、切れの無いものを◎、切れの有るも
のを×とした。
Drawability: Each sample was adhered to the same stainless steel plate as above, and formed into a cylinder with a diameter of 30 mm and a depth of 15 m.
m squeezing process and leaving it in a constant temperature room at 40 ° C for 1 day, then visually observing the floating state of the film, and then
Peel off the film and observe if the peeled film is broken. In the evaluation, the floating state of the film was evaluated as ⊚ without floating, and the floating condition was evaluated as ×, and the presence or absence of breakage of the film was evaluated as ⊚ and the broken condition was evaluated as x.

【0031】剥離作業性:加工後のフィルムを引き剥が
し、きれいに剥がれた場合を○、伸びてしまった場合を
△、切れてしまった場合を×とした。
Peeling workability: The film after processing was peeled off, and when it was peeled off cleanly, it was marked with ◯, when it was stretched, it was marked with Δ, and when it was broken, it was marked with x.

【0032】[0032]

【表1】 [Table 1]

【0033】表1の結果から明らかなように、各実施例
のものは、各機械加工性に優れた評価が得られたのに対
し、比較例1の場合はゴム成分量が極端に少ないので、
絞り加工時に浮きや切れが発生している。比較例2の場
合は結晶化度が高く、応力緩和性に乏しくて絞り加工時
に浮きが発生し、またMFRが極端に大きく、機械的強
度が全般的に低下しており、曲げ加工性が悪く、絞り加
工時の切れも発生している。比較例3の場合は、結晶化
度が低く、曲げ加工性や打ち抜き加工性は、やや不良で
あり、絞り加工性はよいが、剥離時に伸びてしまってい
る。比較例4の場合はゴム成分量が少ないので、応力緩
和性に乏しくて絞り加工時に浮きが発生し、併せて切れ
も発生している。また、比較例5の場合はゴム成分量が
少なく密度も高いので、応力緩和性に乏しくて絞り加工
時に浮きが発生し、併せて切れも発生している。
As is clear from the results shown in Table 1, in each of the examples, an excellent evaluation was obtained in each machinability, whereas in the case of Comparative Example 1, the amount of the rubber component was extremely small. ,
Lifting or breakage occurs during drawing. In the case of Comparative Example 2, the crystallinity is high, the stress relaxation property is poor, floating occurs during drawing, the MFR is extremely large, the mechanical strength is generally lowered, and the bendability is poor. Also, there are some cuts during drawing. In the case of Comparative Example 3, the crystallinity is low, the bending workability and the punching workability are somewhat poor, and the drawing workability is good, but it is elongated at the time of peeling. In the case of Comparative Example 4, since the amount of the rubber component is small, the stress relaxation property is poor, and the floating occurs during the drawing process, and the cutting also occurs. Further, in the case of Comparative Example 5, since the amount of the rubber component is small and the density is high, the stress relaxation property is poor and the floating occurs during the drawing process, and the cutting also occurs.

【0034】[0034]

【発明の効果】本発明の表面保護フィルムは、基材を形
成するポリオレフィン系樹脂として、前記したとおりの
プロピレン系共重合体を用いているので、曲げ加工性、
打ち抜き加工性、絞り加工性等の機械加工性に優れたも
のとなっている。
EFFECTS OF THE INVENTION The surface protective film of the present invention uses the propylene-based copolymer as described above as the polyolefin-based resin for forming the base material, so that the bendability,
It has excellent machinability such as punching workability and drawing workability.

【0035】従って、金属板加工工程を経る被着体の表
面保護、特に機械加工を施すものに用いて好適なもので
ある。しかも、基材としてオレフィン系樹脂フィルムを
使用するから、軟質塩化ビニル系樹脂製フィルムを基材
とするものに比して、焼却時に有毒ガス発生等の問題が
なく、温度依存性か小さいのでシーズンによる基材組成
の変更・調整の必要がなく、比重が小さいので、製品寸
法の大型化が可能であり、現場作業性にも優れている
等、オレフィン系樹脂フィルム使用によるメリットを活
用することができる。
Therefore, it is suitable for use in surface protection of an adherend that has undergone a metal plate processing step, and in particular, for machining. Moreover, since an olefin resin film is used as the base material, there is no problem of toxic gas generation during incineration and temperature dependence is small compared to the one using a soft vinyl chloride resin film as the base material, so the temperature dependence is small. Since there is no need to change or adjust the base material composition due to, and the specific gravity is small, it is possible to increase the product size, and it is also excellent in on-site workability. it can.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 オレフィン系樹脂フィルムからなる基材
の一面に粘着剤層が形成された表面保護フィルムにおい
て、基材を形成するオレフィン系樹脂が、リアクターブ
レンド法により共重合されたプロピレン系共重合体であ
って、該プロピレン系共重合体は、エチレン−プロピレ
ン成分よりなるゴム成分が30〜60重量%であり、該
ゴム成分中のエチレン量が20重量%以上であり、か
つ、結晶化度40〜70%、密度0.885〜0.91
5g/cm3 、MFR5g/10分以下であることを特
徴とする表面保護フィルム。
1. A surface protective film having an adhesive layer formed on one surface of a base material made of an olefin resin film, wherein the olefin resin forming the base material is propylene-based copolymerized by a reactor blending method. In the propylene-based copolymer, the rubber component comprising an ethylene-propylene component is 30 to 60% by weight, the amount of ethylene in the rubber component is 20% by weight or more, and the degree of crystallinity is 40-70%, density 0.885-0.91
A surface protective film having a MFR of 5 g / cm 3 and an MFR of 5 g / 10 minutes or less.
JP16106694A 1994-07-13 1994-07-13 Surface protection film Expired - Fee Related JP3347884B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16106694A JP3347884B2 (en) 1994-07-13 1994-07-13 Surface protection film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16106694A JP3347884B2 (en) 1994-07-13 1994-07-13 Surface protection film

Publications (2)

Publication Number Publication Date
JPH0827445A true JPH0827445A (en) 1996-01-30
JP3347884B2 JP3347884B2 (en) 2002-11-20

Family

ID=15727974

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16106694A Expired - Fee Related JP3347884B2 (en) 1994-07-13 1994-07-13 Surface protection film

Country Status (1)

Country Link
JP (1) JP3347884B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101503978B1 (en) * 2012-08-30 2015-03-18 (주)엘지하우시스 Olefin resin composition for protective film and protection film comprising the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101503978B1 (en) * 2012-08-30 2015-03-18 (주)엘지하우시스 Olefin resin composition for protective film and protection film comprising the same

Also Published As

Publication number Publication date
JP3347884B2 (en) 2002-11-20

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