JPS5815580A - Surface protecting film - Google Patents
Surface protecting filmInfo
- Publication number
- JPS5815580A JPS5815580A JP11458681A JP11458681A JPS5815580A JP S5815580 A JPS5815580 A JP S5815580A JP 11458681 A JP11458681 A JP 11458681A JP 11458681 A JP11458681 A JP 11458681A JP S5815580 A JPS5815580 A JP S5815580A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- film
- layer
- force
- base material
- 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
Landscapes
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は鋼板、化粧板等板材の表面保護フィルムに係る
ものである。鋼板、化粧板等の板材は家具、電化製品等
その用途は多岐に及ぶが、流通、加工時における表面保
護、防錆等の目的で表面保護フィルムをラミネートして
いる場合が多く見られる。表面保護フィルムは通常最終
製品においては板材より剥離して用いられる為、
(1)板材に対し適当な接着強度を有し、流通、エンボ
ス、曲げ等の2次加工時に剥離がなくかつ使用後容易に
剥し得る事。 1(2)板材
に対し汚染性がない事。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a surface protection film for plate materials such as steel plates and decorative plates. Plate materials such as steel plates and decorative laminates have a wide range of uses, including furniture and electrical appliances, but they are often laminated with a surface protection film for purposes such as surface protection and rust prevention during distribution and processing. Since the surface protection film is usually used after being peeled off from the plate material in the final product, (1) it has appropriate adhesive strength to the plate material, does not peel off during secondary processing such as distribution, embossing, bending, etc., and is easy to use after use. Things that can be peeled off. 1(2) No contamination to the plate material.
(3)透明性を有l−板材表面が透視できる事。(3) Transparency - The surface of the plate material can be seen through.
(4)適当な耐候性を有し紫外線、熱等による劣化が少
ない事。(4) Appropriate weather resistance and little deterioration due to ultraviolet rays, heat, etc.
などの性能が要求され、従来この様な保護フィルムの製
造は例えばポリエチレン、ポリ塩化ビニル等&’)フィ
ルムにアクリル系、ゴム系等の粘着剤を塗布する事によ
り行われていたが、表面保循フィルムは前記の如く通常
最終製品に於いては剥離して使用される為板材表面へ貼
り付けた場合の接着強度はあまり大きすぎてはならず、
約数子9/インチ〜数百9/インチの範囲が適当とされ
ている。粘着力に関する十分な理論的解析は現在の所さ
れているとは言い難いが、被着体に対する粘着剤の接着
力は、大まかには被着体に対する濡れ即ち粘着剤の投錨
力と粘着剤のもつ凝集力より形成されていると言ってよ
い。一方表面保論フイルムに望まれている粘着力は前記
の様に比較的弱いものとされているがこの部は、とりも
なおさず粘着剤σ)投錨力もしくは凝集力を弱める他な
らない。Conventionally, such protective films were manufactured by coating polyethylene, polyvinyl chloride, etc. films with acrylic or rubber adhesives, etc. As mentioned above, the circulation film is usually used after being peeled off in the final product, so the adhesive strength when pasting it to the surface of the board must not be too high.
A range of about 9/inch to several hundred 9/inch is considered appropriate. Although it cannot be said that sufficient theoretical analysis regarding adhesive force has been carried out at present, the adhesive force of an adhesive to an adherend is roughly determined by the wetting of the adherend, that is, the anchoring force of the adhesive, and the adhesive's anchoring force. It can be said that it is formed due to the cohesive force that it has. On the other hand, the desired adhesive strength of the surface-adhesive film is said to be relatively weak as described above, but this part has no choice but to weaken the anchoring force or cohesive force of the adhesive σ).
又、表面保護フィルムは被着体である板材表面の保護を
目的とするもので、前記の如く板材表面を汚染するもの
であってはならないが、接着力を調整する為、粘着剤の
凝集力を弱めた場合、剥離時粘着剤の凝集力が弱い為粘
着剤自身θ)凝集破壊や可塑剤等の添加剤のブリード即
ち被着体に粘着力凝集力の大きい粘着剤を使用した場合
、被着体への投錨力を極度に低下させ、有効な接着力が
得られないか、被着体に対する接着力が大きすぎ、剥離
時の作業性を著しくそこねるという問題があった。表面
保護フィルムに供する粘着剤は被着体に対し適当な投錨
力をもちかつ剥離力のより大きな凝集力を有する事が必
要である。In addition, the purpose of the surface protection film is to protect the surface of the plate material to which it is adhered, and as mentioned above, it must not contaminate the surface of the plate material.However, in order to adjust the adhesive strength, the cohesive force of the adhesive If the adhesive is weakened, the cohesive force of the adhesive will be weak during peeling, resulting in cohesive failure of the adhesive itself (θ) or bleeding of additives such as plasticizers. There is a problem in that the anchoring force to the adherend is extremely reduced, and effective adhesive force cannot be obtained, or the adhesive force to the adherend is too large, which significantly impairs workability during peeling. The adhesive used in the surface protection film needs to have a suitable anchoring force to the adherend and a cohesive force with a greater peeling force.
本発明はこσ)様な問題点を解決すべ(考案されたもの
で、粘着剤の持つ大きい凝集力を維持しつつ被着体への
接着力を弱め、適当な強度保持を計るもので、基材層/
粘着層もしくは背面処理された基材層/粘着層の2層以
上より成り、かつ粘着3一
層に粒径5μ乃至301tの無機充填剤をo5〜20重
量係添加して成る表面保護フィルムで力)る。The present invention was devised to solve the above problems, and aims to maintain appropriate strength by weakening the adhesive force to the adherend while maintaining the large cohesive force of the adhesive. Base material layer/
A surface protection film consisting of two or more layers of an adhesive layer or a back-treated base material layer/adhesive layer, and in which an inorganic filler with a particle size of 5 μ to 301 t is added to the adhesive layer in an amount of 05 to 20% by weight. Ru.
本発明は、粘着剤層に無機充填剤を添加して成るため、
粘着剤表面て微細な凹凸を形成せしめ、粘着剤と被着体
の接触面積を減じ、その結果粘着剤の凝集力を維持しつ
つ被着体への接着力を調整せしめるもθ)である。Since the present invention is made by adding an inorganic filler to the adhesive layer,
Fine irregularities are formed on the surface of the adhesive to reduce the contact area between the adhesive and the adherend, thereby adjusting the adhesive force to the adherend while maintaining the cohesive force of the adhesive.
本発明をさらに詳しく説明すれば、用いらAする基材層
は例えばポリエチレン、ポリプロピレン、ポリ塩化ビニ
ル等のフィルムであり、通常60〜200μ程度の厚み
のものが使用されるが、勿論フィルム形成が可能である
ならば、これらに限るものではない。保護フィルムはこ
の様な基材に粘着剤を塗布し、通常剥離紙等を用いず、
そのまま巻取られる事が多く、被着体である板材へ貼付
ける場合、その巻取り状のものを巻きもどして使用する
が、粘着剤と基材層が接着するブロッキング現象が生じ
、巻もどし時の作業性を低下させる事があるため背面処
理を行ってもよい。背面処理とは、基材表面(粘着剤を
塗布していない面)に粘4−
着剤の投錨力を減じさせ、接着力を弱め、巻もどし、作
業性を改良するもので、基材表面にシリコーン誘導体、
長鎖アルキル化合物、パーフロロアルキル化合物等の処
理剤を塗布もしくは脂肪酸アミド、ワックス等の有機滑
剤もしくは後記無機充填剤を配合する事により処理効果
が得られる。To explain the present invention in more detail, the base material layer used is, for example, a film of polyethylene, polypropylene, polyvinyl chloride, etc., and a film having a thickness of about 60 to 200 μm is usually used, but of course it is difficult to form a film. If possible, it is not limited to these. Protective films are made by applying adhesive to such a base material, and usually without using release paper, etc.
It is often rolled up as it is, and when pasting it on a board material to be adhered to, the rolled version is unwound and used, but a blocking phenomenon occurs in which the adhesive and the base material layer adhere, and when unrolled, Since this may reduce workability, back surface treatment may be performed. Back treatment is a process that reduces the anchoring force of the adhesive on the surface of the base material (the side that is not coated with adhesive), weakens the adhesive strength, and improves unwinding and workability. silicone derivatives,
A treatment effect can be obtained by applying a treatment agent such as a long-chain alkyl compound or perfluoroalkyl compound, or by incorporating an organic lubricant such as fatty acid amide or wax, or an inorganic filler as described below.
さらに用いられる粘着剤は、天然ゴム、イソグレンゴム
、スチレンブタジェンゴム、スチレン系ブロック共重合
ゴム(SIS、5BS)、xfvンプロピレンゴム、エ
チレン酢酸ビニル共重合樹脂等のゴムもしくはエラスト
マーに、ロジン、テルペン樹脂、石油樹脂、クマロンイ
ンデン樹脂等の粘着付与剤を配合して成る粘着樹脂、も
しくはアクリル系粘着剤等の粘着樹脂に、メルク(滑石
)ケイソ士、酸化ケイ素、カオリン(陶土)、酸化アル
ミニウム、酸化亜鉛、炭酸カルシウム、炭酸マグネシウ
ム、硫酸カルシウム、硫酸バリウム等の無機充填剤を配
合して成るものである。この無機充填剤は粘着剤に配合
され、粘着剤表面に微細な凹凸を形成せしめる事により
被着体との接着面5−
積を減じ、その結果粘着剤の凝集力を維持しつつ被着体
への接着力を調整せしめるもので、平均粒径5〜30μ
の粉末状のものを添加量01〜20重量係の範囲内で使
用出来るが、こい様な無機系添加剤は添加量を太き(し
た場合、樹脂本来の透明性を低下させる事があるため、
好ましくは15重量係以下の添加量で使用すべきであり
本発明主旨である粘着剤の接着力調整効果は前記無機充
填剤中タルクが最も秀れている。この様な無機充填剤の
粘着剤中への配合は押出機バンバリーミキサ−13本ロ
ール、ニーダ−等の熱溶融混線法、ボールミルアトライ
ター、サンドミル等の溶融混線法等の手段により達成さ
れる。Furthermore, the adhesive used is rubber or elastomer such as natural rubber, isogrene rubber, styrene butadiene rubber, styrene block copolymer rubber (SIS, 5BS), xfv propylene rubber, ethylene vinyl acetate copolymer resin, rosin, terpene, etc. Adhesive resin made by blending a tackifier such as resin, petroleum resin, coumaron indene resin, or adhesive resin such as acrylic adhesive, Merck (talc) silica, silicon oxide, kaolin (pottery clay), aluminum oxide. , zinc oxide, calcium carbonate, magnesium carbonate, calcium sulfate, barium sulfate, and other inorganic fillers. This inorganic filler is blended into the adhesive and forms fine irregularities on the surface of the adhesive, thereby reducing the area of the bonding surface with the adherend, thereby maintaining the cohesive force of the adhesive. It adjusts the adhesive force to
Powdered additives can be used within the range of 0.1 to 20% by weight, but inorganic additives like this can be added in large amounts (as this may reduce the original transparency of the resin). ,
Talc should preferably be used in an amount of 15% by weight or less, and among the inorganic fillers, talc has the best effect of adjusting the adhesive strength of the adhesive, which is the gist of the present invention. Incorporation of such an inorganic filler into the pressure-sensitive adhesive is achieved by means such as a hot melt mixing method using an extruder, a Banbury mixer with 13 rolls, a kneader, etc., a melt mixing method using a ball mill attritor, a sand mill, etc.
この様な本発明に於ける粘着剤は基材ヘグラビアコート
、ロールコート等の溶液コーティング又はホントメルト
コーティング、押出しコーティング等の熱溶融コーティ
ング法により基材へ塗布されるが、共押出し法を用い、
基材層/粘着剤層もしくは背面処理層/基材層/粘着剤
層の6層以上を同時に押出し、フィルム状とする事も可
能であ= 6一
この様にして製造された表面保護フィルムは粘着剤の凝
集力を低下させる事なしに被着体である板材との接着力
を調節したもので保護フィルムとして使用完了後に容易
に剥離する事が可能でしがも被着体への糊残りによる表
面汚染を防止する事が可能となる。The adhesive in the present invention is applied to the substrate by solution coating such as gravure coating or roll coating, or by hot melt coating such as true melt coating or extrusion coating, but it is possible to apply the adhesive to the substrate by using a coextrusion method. ,
It is also possible to simultaneously extrude six or more layers of base material layer/adhesive layer or back treatment layer/base material layer/adhesive layer to form a film = 6 - The surface protection film produced in this way is The adhesive strength to the adherend plate material is adjusted without reducing the cohesive force of the adhesive, and it can be easily peeled off after use as a protective film, but does not leave any adhesive residue on the adherend. This makes it possible to prevent surface contamination caused by
以下本発明による実施例について記載する。Examples according to the present invention will be described below.
実施例−1
(1)粘着剤層 配合比(重重1粘着
剤処方(重量比)
(2)基材層
低密度ポリエチレン
(ミラノン12;三井ポリケミカル■)(3)背面処理
層
低密度ポリエチレン
(ミラノン12;三井ポリケミカル■)タルク(SWA
(平均粒径20μ);朝日製粉■)上記(1)〜(3)
の樹脂配合処方を用いた。(1)の粘着剤層については
、A、Bを配合に■〜■の樹脂処方とした。Example-1 (1) Adhesive layer blending ratio (heavy weight 1 adhesive formulation (weight ratio)) (2) Base material layer low density polyethylene (Milanon 12; Mitsui Polychemical ■) (3) Back treatment layer low density polyethylene ( Milanon 12; Mitsui Polychemical ■) Talc (SWA
(Average particle size 20 μ); Asahi Flour ■) (1) to (3) above
The following resin formulation was used. For the pressure-sensitive adhesive layer (1), A and B were added to the resin formulations ① to ②.
次いで共押出装置を用い、200°C(1)加工温度に
より、接着剤層20μ、基材層30μ、背面処理層10
μの3層溶融フィルムを冷却ロール上に押出し6層フィ
ルムを得た。得られたフィルムをトリクレンで洗浄した
05w++厚みのアルミニウム板にゴムロール間を通し
、アルミニウム板に貼付け、テンシロン(東洋ボールド
ウィン■製)Kより剥離強度を測定した。(表−1)
表−1
実施例−2
アクリル系粘着剤(BPS3841 ;20係酢酸エチ
ル浴液;東洋インキ製造■製)100部に対し、実施例
−1と同様のメルク5重量部を添加し、ボールミルによ
り24時間混合分散を行った(粘着剤■とする)。この
溶液を版深iooμのグラビア版により予め片面にコロ
ナ放電を行い、かつコロナ処理面に対しポリイソシアネ
ート(日本ポリウレタン■;コロネートr、) 10%
酢酸エチル溶液を塗布した低密度ポリエチレンフィルム
60μにコーティングを行った。又比較例としてタルク
を添加していない粘着剤(粘着剤■とする)な上記と同
様手順により低密度ポリエチレンにコーティングを行っ
た。さらに得られた粘着剤塗布フィルムを実施例−1に
示した手順によりアルミニウム板に貼付け、その剥離強
度を測定した(表−2)。Next, using a coextrusion device, a processing temperature of 200°C (1) was used to form an adhesive layer of 20μ, a base material layer of 30μ, and a back treatment layer of 10μ.
The 3-layer molten film of μ was extruded onto a cooling roll to obtain a 6-layer film. The obtained film was passed between rubber rolls on an aluminum plate having a thickness of 05w++ which had been washed with trichlene, and was attached to the aluminum plate, and the peel strength was measured using Tensilon K (manufactured by Toyo Baldwin ■). (Table-1) Table-1 Example-2 5 parts by weight of Merck as in Example-1 was added to 100 parts of acrylic pressure-sensitive adhesive (BPS3841; ethyl acetate bath solution of 20%; manufactured by Toyo Ink Manufacturing Co., Ltd.). Then, mixing and dispersion was carried out for 24 hours using a ball mill (referred to as adhesive ①). This solution was subjected to corona discharge on one side in advance using a gravure plate with a plate depth of ioμ, and 10% polyisocyanate (Japan Polyurethane ■; Coronate R) was applied to the corona-treated side.
A 60μ low density polyethylene film coated with an ethyl acetate solution was coated. As a comparative example, low-density polyethylene was coated with an adhesive to which no talc was added (referred to as adhesive ①) using the same procedure as above. Further, the obtained adhesive-coated film was attached to an aluminum plate according to the procedure shown in Example 1, and its peel strength was measured (Table 2).
表−2 特許出願人Table-2 patent applicant
Claims (1)
層/粘着層の2層以上より成り、かつ粘着層に粒径5μ
乃至30μの無機充填剤を05〜20係添加して成る表
面保護フィルム。(1) Consists of two or more layers: base material layer/adhesive layer, or back-treated base material layer/adhesive layer, and the adhesive layer has a particle size of 5 μm.
A surface protection film containing an inorganic filler with a thickness of 05 to 20 μm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11458681A JPS5815580A (en) | 1981-07-22 | 1981-07-22 | Surface protecting film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11458681A JPS5815580A (en) | 1981-07-22 | 1981-07-22 | Surface protecting film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5815580A true JPS5815580A (en) | 1983-01-28 |
Family
ID=14641554
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11458681A Pending JPS5815580A (en) | 1981-07-22 | 1981-07-22 | Surface protecting film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5815580A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01145471U (en) * | 1988-03-30 | 1989-10-05 | ||
| JPH01145470U (en) * | 1988-03-30 | 1989-10-05 | ||
| JPH03109882U (en) * | 1990-02-26 | 1991-11-12 | ||
| JPH05185768A (en) * | 1992-03-30 | 1993-07-27 | Toppan Moore Co Ltd | Confidential information hiding member |
| JPH079782A (en) * | 1993-06-28 | 1995-01-13 | Toppan Moore Co Ltd | Concealed information possession |
| WO2002036698A3 (en) * | 2000-11-06 | 2003-02-27 | Schulman A Inc | Polyolefin film for use as a non-staining masking film |
| JP2008265307A (en) * | 2007-03-22 | 2008-11-06 | Japan Polypropylene Corp | Propylene surface protective film |
| JP2009196334A (en) * | 2007-03-22 | 2009-09-03 | Japan Polypropylene Corp | Film for surface protection |
| JP2009208416A (en) * | 2008-03-06 | 2009-09-17 | Japan Polypropylene Corp | Propylene resin film for surface protection |
| CN108047588A (en) * | 2017-11-20 | 2018-05-18 | 安徽天安新材料有限公司 | The preparation method of cold lamination film |
| CN108178885A (en) * | 2017-11-20 | 2018-06-19 | 安徽天安新材料有限公司 | The feedstock composition and cold lamination film of cold lamination film |
-
1981
- 1981-07-22 JP JP11458681A patent/JPS5815580A/en active Pending
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01145471U (en) * | 1988-03-30 | 1989-10-05 | ||
| JPH01145470U (en) * | 1988-03-30 | 1989-10-05 | ||
| JPH03109882U (en) * | 1990-02-26 | 1991-11-12 | ||
| JPH05185768A (en) * | 1992-03-30 | 1993-07-27 | Toppan Moore Co Ltd | Confidential information hiding member |
| JPH079782A (en) * | 1993-06-28 | 1995-01-13 | Toppan Moore Co Ltd | Concealed information possession |
| WO2002036698A3 (en) * | 2000-11-06 | 2003-02-27 | Schulman A Inc | Polyolefin film for use as a non-staining masking film |
| JP2008265307A (en) * | 2007-03-22 | 2008-11-06 | Japan Polypropylene Corp | Propylene surface protective film |
| JP2008265308A (en) * | 2007-03-22 | 2008-11-06 | Japan Polypropylene Corp | Propylene surface protective film |
| JP2009196334A (en) * | 2007-03-22 | 2009-09-03 | Japan Polypropylene Corp | Film for surface protection |
| JP2009208416A (en) * | 2008-03-06 | 2009-09-17 | Japan Polypropylene Corp | Propylene resin film for surface protection |
| CN108047588A (en) * | 2017-11-20 | 2018-05-18 | 安徽天安新材料有限公司 | The preparation method of cold lamination film |
| CN108178885A (en) * | 2017-11-20 | 2018-06-19 | 安徽天安新材料有限公司 | The feedstock composition and cold lamination film of cold lamination film |
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