JPH07116410B2 - Adhesive film for surface protection - Google Patents
Adhesive film for surface protectionInfo
- Publication number
- JPH07116410B2 JPH07116410B2 JP59226463A JP22646384A JPH07116410B2 JP H07116410 B2 JPH07116410 B2 JP H07116410B2 JP 59226463 A JP59226463 A JP 59226463A JP 22646384 A JP22646384 A JP 22646384A JP H07116410 B2 JPH07116410 B2 JP H07116410B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- film
- surface protection
- present
- polyolefin resin
- 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 - Lifetime
Links
- 239000002313 adhesive film Substances 0.000 title claims description 13
- 239000012790 adhesive layer Substances 0.000 claims description 14
- 229920005672 polyolefin resin Polymers 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 description 22
- 230000001070 adhesive effect Effects 0.000 description 21
- 238000004873 anchoring Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 7
- -1 polyethylene Polymers 0.000 description 6
- 239000010410 layer Substances 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 229920002633 Kraton (polymer) Polymers 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、金属板、ガラス板、合成樹脂板などの板状物
品の表面に剥離自在に粘着されて、これら物品の表面が
傷付けられたり、ゴミなどが付着したりするのを防止す
る表面保護用接着フィルムに関するものである。さらに
詳しくは、板状物品に粘着されて比較的長時間放置され
ても接着力の経日変化が少なく、常時容易に剥離除去で
きる程度の接着力を維持することができる表面保護用接
着フィルムに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention is such that the surface of a plate-like article such as a metal plate, a glass plate, a synthetic resin plate or the like is releasably adhered to the article so that the surface of the article may be damaged. The present invention relates to an adhesive film for surface protection which prevents dust and the like from adhering. More specifically, the present invention relates to an adhesive film for surface protection which is adhered to a plate-like article and has little change with time in adhesive strength even when left for a relatively long time, and which can maintain an adhesive strength that can be easily peeled and removed at all times. .
従来、表面保護用接着フィルム用の粘着剤としては、ア
クリル系粘着剤や天然ゴム、ポリイソブチレンなどのゴ
ムを主体とするゴム系粘着剤が汎用されてきたが、これ
らは溶剤系のものであるため、表面保護用接着フィルム
製造時の安全衛生性、公害、経済性などに問題点があっ
た。近年、これらの問題点を改善するために粘着剤の無
溶剤化が要望されており、その有力な手段の一つとして
接着剤層と支持体フィルム(ポリオレフィン樹脂フィル
ム)を共押出しによって製造する手法が種々検討されて
いる。しかしながら、この共押出しによる製造方式で
は、難接着材料の代表であるポリエチレン、ポリプロピ
ロピレン等のオレフィン樹脂フィルムと接着剤層との接
着性(投錨性)を上げるための有力な手段であるコロナ
処理、アルカリ処理、火炎処理等が行えない為、投錨性
の良好な共押出フィルムを得ることが極めて困難であ
る。従って、当該フィルムを金属板などに仮着して板金
加工を施すと投錨力が小さいため、支持層フィルムと接
着剤層との間で界面破壊を生じ、糊残りが発生するとい
う問題点がある。Conventionally, as a pressure-sensitive adhesive for an adhesive film for surface protection, an acrylic pressure-sensitive adhesive, a natural rubber, a rubber-based pressure-sensitive adhesive mainly composed of rubber such as polyisobutylene has been widely used, but these are solvent-based. Therefore, there are problems in safety and hygiene, pollution, economy, etc. during the production of the surface protection adhesive film. In recent years, solvent-free adhesives have been demanded in order to improve these problems, and as one of the effective means, a method of producing an adhesive layer and a support film (polyolefin resin film) by coextrusion Are being studied. However, in this manufacturing method by co-extrusion, polyethylene, which is a representative of difficult-to-adhesive materials, corona treatment, which is a powerful means for increasing the adhesiveness (anchoring property) between an olefin resin film such as polypropylene and polypropylene and an adhesive layer, Since alkali treatment, flame treatment, etc. cannot be performed, it is extremely difficult to obtain a coextruded film having good anchoring properties. Therefore, when the film is temporarily attached to a metal plate or the like and subjected to sheet metal processing, the anchoring force is small, so that there is a problem that interface destruction occurs between the support layer film and the adhesive layer, and adhesive residue occurs. .
この問題点を解決するために、ポリオレフィン樹脂フィ
ルムとの親和性の高いエチレンを主成分とする共重合
体、例えばEVAを接着剤層とした共押出フィルムが提案
されているが、酢酸ビニル含有量が極めて低いものにつ
いては十分な投錨力が得られるが、粘着性がほとんどな
く、高接着なものが得られないという問題がある。一
方、SBB.SIS等のブロックポリマーとポリオレフィン樹
脂フィルムとの共押出が提案されており、これらの系で
は比較的投錨力の優れたものは得られるが、長期保存す
ると劣化を生じやすく擬集力の低下により糊残りが生じ
るという問題点があり、いずれの場合においても、糊残
り性について満足できるものが見当たらないというのが
実情である。In order to solve this problem, a copolymer containing ethylene as a main component, which has a high affinity with a polyolefin resin film, for example, a coextrusion film having EVA as an adhesive layer has been proposed. Those having an extremely low value can obtain sufficient anchoring force, but have a problem in that they have almost no tackiness and cannot be highly adhered. On the other hand, coextrusion of a block polymer such as SBB.SIS and a polyolefin resin film has been proposed, and although these systems have relatively excellent anchoring power, they tend to deteriorate when stored for a long period of time, and the pseudo-aggregation force tends to occur. However, there is a problem that adhesive residue is generated due to the decrease in the adhesiveness, and in any case, no satisfactory adhesive residue is found.
本発明の目的は、投錨力が極めて優れ、長期保存しても
糊残りが生じず、かつ共押出による製造も可能な表面保
護フィルムを提供することである。An object of the present invention is to provide a surface protective film that has an excellent anchoring force, does not cause adhesive residue even after long-term storage, and can be manufactured by coextrusion.
本発明者らは、上記の如き困難な問題点を解決すべく種
々の材料について検討した結果、A−B−A(但し、A
はスチレン重合体ブロックを、Bはエチレンとブチレン
との重合体ブロックを示す)を主成分として、これに特
定量以下の粘着付与樹脂を配合してなる接着剤層をポリ
オレフィン樹脂フィルム上に形成させてなる表面保護用
接着フィルムが上記目的を解決しうるものであることを
見出して本発明を完成するに至った。即ち、本発明は一
般式、A−B−A(但し、AおよびBは前記と同意義で
ある)100重量部と粘着性付与樹脂0〜80重量部を含有
する組成物よりなる接着剤層をポリオレフィン樹脂フィ
ルム上に形成させてなる表面保護用接着フィルムよりな
るものである。The present inventors have studied various materials in order to solve the above-mentioned difficult problems, and as a result, A-B-A (however, A
Is a styrene polymer block, B is a polymer block of ethylene and butylene) as a main component, and an adhesive layer is formed on the polyolefin resin film by adding a tackifying resin in a specific amount or less. The present invention has been completed by finding that the adhesive film for surface protection formed as described above can solve the above object. That is, the present invention provides an adhesive layer comprising a composition containing 100 parts by weight of the general formula, A-B-A (where A and B have the same meanings as described above), and 0 to 80 parts by weight of a tackifying resin. Is formed on a polyolefin resin film, and is formed of an adhesive film for surface protection.
本発明で使用されるA−B−AにおけるAは、スチレン
重合体ブロックであるが、その好ましい分子量は2000〜
100000程度であり、またその好ましいガラス転移温度
は、20℃以上である。また、A−B−AにおけるBは、
エチレンとブチレンとの共重合体ブロックであるが、そ
の好ましい分子量は10000〜300000程度であり、またそ
の好ましいガラス転移温度は、−20℃以下である。Aお
よびBの好ましい重量比は、A/B=5/95〜50/50である。
A−B−Aの好ましい例としては、例えば、Shell化学
社製のクレイトンG−1650、クレイトンG−1652等が挙
げられる。A in A-B-A used in the present invention is a styrene polymer block whose preferred molecular weight is 2000-
It is about 100000, and its preferable glass transition temperature is 20 ° C. or higher. Also, B in A-B-A is
Although it is a copolymer block of ethylene and butylene, its preferred molecular weight is about 10,000 to 300,000, and its preferred glass transition temperature is -20 ° C or lower. The preferred weight ratio of A and B is A / B = 5/95 to 50/50.
Preferable examples of ABA include Kraton G-1650 and Kraton G-1652 manufactured by Shell Chemical Co., Ltd.
本発明においては、A−B−Aに加えて、さらにA−B
を配合してもよい。In the present invention, in addition to A-B-A, further A-B
You may mix | blend.
A−BにおけるAおよびBの定義は前記と同様であり、
AとBの重量比は、A/B=5/95〜50/50が好ましい。A−
B−AとA−Bとの混合物の例としては、例えば、Shel
l化学社製のクレイトンG−1657などが挙げられる。The definitions of A and B in AB are the same as above,
The weight ratio of A and B is preferably A / B = 5/95 to 50/50. A-
As an example of the mixture of BA and AB, for example, Shel
Examples include Kraton G-1657 manufactured by Kagaku.
本発明で使用される粘着付与性樹脂としては、目的に応
じて種々のものを用いることができるが、一般的には、
相溶性がよく、粘着力を向上しうる特性を有するものが
使用される。具体的には、たとえばフェノール樹脂、ロ
ジン、ピネン樹脂、石油樹脂、スチレン樹脂、クマロン
樹脂等が適している。その添加量は、A−B−A(A−
B−AとA−B混合物を含む)100重量部に対して0〜8
0重量部、好ましくは20〜60重量部の範囲である。粘着
付与性樹脂が80重量部を越えると長期貼付け後の接着力
の上昇が著しく、剥離の際に糊残りを生じやすい。As the tackifying resin used in the present invention, various resins can be used depending on the purpose, but generally,
A material having a good compatibility and a property capable of improving the adhesive strength is used. Specifically, for example, phenol resin, rosin, pinene resin, petroleum resin, styrene resin, coumarone resin and the like are suitable. The addition amount is A-B-A (A-
(Including B-A and A-B mixture) 0 to 8 per 100 parts by weight
The amount is 0 part by weight, preferably 20 to 60 parts by weight. If the tackifying resin exceeds 80 parts by weight, the adhesive strength after a long-term sticking will remarkably increase, and adhesive residue tends to occur during peeling.
また、本発明において用いられるポリオレフィン系樹脂
フィルムとしては、溶融押出して表面保護フィルムの支
持体となりうる材料にて構成されていることが好まし
い。かかるものの例としては、コスト面等から、ポリエ
チレン、ポリプロピレンなどよりなるものが好適であ
る。The polyolefin resin film used in the present invention is preferably composed of a material that can be melt-extruded to serve as a support for the surface protection film. As an example of such a material, a material made of polyethylene, polypropylene or the like is preferable in terms of cost.
接着剤層には、さらに目的に応じて、通常用いられる各
種ゴム、軟化剤、充填剤、紫外線吸収剤、老化防止剤の
如き各種材料を本発明の主旨に反しない範囲で使用して
もよい。For the adhesive layer, various materials such as various rubbers, softeners, fillers, ultraviolet absorbers, and antioxidants that are commonly used may be used according to the purpose within the range not departing from the gist of the present invention. .
本発明の表面保護用接着フィルムの各層の厚みは、好ま
しくは次の通りである。即ち、接着剤層は、好ましくは
200μ以下、より好ましくは5〜50μであり、ポリオレ
フィン樹脂フィルム層は、300μ以下、好ましくは10〜1
00μである。The thickness of each layer of the adhesive film for surface protection of the present invention is preferably as follows. That is, the adhesive layer is preferably
200μ or less, more preferably 5 to 50μ, the polyolefin resin film layer is 300μ or less, preferably 10 to 1
It is 00μ.
本発明表面保護用接着フィルムの製造は、たとえば次に
のようにして行われる。即ち、接着剤成分と熱可塑性合
成樹脂とを、溶融共押出し装置にて、二つの流れにし
て、即ち、支持体フィルム形成用流体と接着剤層形成用
流体とをダイス口内で合流せしめて単一流体を形成して
押出し、接着剤層とポリオレフィン樹脂フィルム層とを
複合することによって製造される。勿論、接着剤層構成
組成物をポリオレフィン樹脂フィルムに塗布することに
よっても容易に製造することが出来る。The surface protective adhesive film of the present invention is produced, for example, as follows. That is, the adhesive component and the thermoplastic synthetic resin are made into two streams by a melt co-extrusion device, that is, the support film forming fluid and the adhesive layer forming fluid are combined in a die opening to form a single stream. It is manufactured by forming one fluid, extruding, and compounding the adhesive layer and the polyolefin resin film layer. Of course, it can be easily produced by applying the adhesive layer constituent composition to the polyolefin resin film.
本発明の方法によって得られた表面保護フィルムは、接
着層のポリオレフィン樹脂フィルムに対する投錨力に優
れており、表面保護フィルム金属板などに仮着して板金
加工したり、長期間そのまま放置したりしても糊残りが
生じない顕著な特徴を有するものである。より具体的に
は、後記実験例から明らかなように、本発明表面保護用
接着フィルムは投錨力がいずれも2000g/20mm以上あり、
加工後の糊残りは全く認められない。また、長期間、貼
合せて保存しても、接着剤層の劣化はほとんどなく、糊
残りは、全く認められず、顕著な効果を有する。The surface protective film obtained by the method of the present invention is excellent in anchoring force to the polyolefin resin film of the adhesive layer, and is temporarily attached to the surface protective film metal plate or the like for sheet metal processing, or may be left as it is for a long time. However, it has a remarkable characteristic that adhesive residue does not occur. More specifically, as is clear from the experimental examples described below, the surface protective adhesive film of the present invention has an anchoring force of 2000 g / 20 mm or more,
No glue residue is observed after processing. Further, even when the pieces are laminated and stored for a long period of time, the adhesive layer is hardly deteriorated, and no adhesive residue is observed at all, which is a remarkable effect.
以下、本発明の実施例を示すが、本発明はこれら実施例
によって何等限定されるものではない。実施例1〜3・
比較例1〜2 第1表に示した接着剤成分、ポリオレフィン樹脂(ポリ
オレフィン樹脂形成用)を用いて第1表に記載の条件下
に第1表記載の各層厚を有する表面保護用接着フィルム
を得た。Examples of the present invention will be shown below, but the present invention is not limited to these examples. Examples 1-3
Comparative Examples 1-2 Using the adhesive components and polyolefin resin (for forming polyolefin resin) shown in Table 1, under the conditions shown in Table 1, adhesive films for surface protection having the respective layer thicknesses shown in Table 1 were prepared. Obtained.
実験例1 上記で得た各表面保護用接着フィルムについて投錨力、
貼付後の糊残り、接着力および加工後の糊残りを調べ、
その結果を第1表に示した。Experimental Example 1 Anchoring force of each surface protection adhesive film obtained above,
Examine the adhesive residue after pasting, adhesive strength and adhesive residue after processing,
The results are shown in Table 1.
第1表中の評価方法 投錨力:試料片を糊面同士で圧着後70℃中に1時間保存
し、20℃×65%相対湿度(R.H.)中で180度引き剥がし
試験を行って測定した。Evaluation method in Table 1 Anchoring force: Measured by performing a 180 degree peeling test in 20 ° C x 65% relative humidity (RH) after storing the sample pieces for one hour after bonding them to each other with glue surfaces .
引き剥がし速度は300mm/minである。The peeling speed is 300 mm / min.
接着力:SUS304ステンレス板に試料片を貼り付け、180度
引き剥がし試験を行って測定した。引き剥がし速度は30
0mm/minである。Adhesion: A sample piece was attached to a SUS304 stainless steel plate, and a 180 degree peeling test was performed to measure. Peeling speed is 30
It is 0 mm / min.
貼り付け後の糊残り:SUS304ステンレス板に試料片を貼
り付けて、40℃中に6ヶ月放置後、20℃×65%相対湿度
(R.H.)中で糊残りの有無を観察した。Adhesive residue after application: A sample piece was attached to a SUS304 stainless steel plate, left at 40 ° C for 6 months, and then observed for adhesive residue at 20 ° C x 65% relative humidity (RH).
加工後の糊残り:厚さ0.4mmのSUS304ステンレス板に試
料片を貼り付け、これを試料片がダイス側になるように
金型にセットし、50mmΦのポンチで20mmの深さに絞りス
テンレス板面への糊残りを観察した。Adhesive residue after processing: Stick a sample piece on a SUS304 stainless steel plate with a thickness of 0.4 mm, set it in the mold so that the sample piece will be on the die side, and squeeze it to a depth of 20 mm with a punch of 50 mmΦ Stainless steel plate The adhesive residue on the surface was observed.
Claims (1)
ロックを、Bはエチレンとブチレンとの共重合体ブロッ
クを示す)100重量部と粘着付与性樹脂0〜80重量部を
含有する組成物よりなる接着剤層を、ポリオレフィン樹
脂フィルム上に形成させてなる表面保護用接着フィル
ム。1. ABA containing 100 parts by weight (where A is a styrene polymer block and B is a copolymer block of ethylene and butylene) and 0 to 80 parts by weight of a tackifying resin. An adhesive film for surface protection, which is formed by forming an adhesive layer made of the composition described above on a polyolefin resin film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59226463A JPH07116410B2 (en) | 1984-10-27 | 1984-10-27 | Adhesive film for surface protection |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59226463A JPH07116410B2 (en) | 1984-10-27 | 1984-10-27 | Adhesive film for surface protection |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61103975A JPS61103975A (en) | 1986-05-22 |
JPH07116410B2 true JPH07116410B2 (en) | 1995-12-13 |
Family
ID=16845490
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59226463A Expired - Lifetime JPH07116410B2 (en) | 1984-10-27 | 1984-10-27 | Adhesive film for surface protection |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07116410B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9873788B2 (en) | 2014-04-08 | 2018-01-23 | Asahi Kasei Kabushiki Kaisha | Composition and surface protection film |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5232787A (en) * | 1990-06-08 | 1993-08-03 | Sekisui Chemical Co., Ltd. | Method of making a pressure sensitive adhesive tape or sheet |
US5571864A (en) * | 1993-03-23 | 1996-11-05 | Regents Of The University Of Minnesota | Miscible polyolefin blends with modifying polyolefin having matching segment lengths |
US5654364A (en) * | 1993-03-23 | 1997-08-05 | Regents Of The University Of Minnesota | Miscible blend of polyolefin and polyolefin block copolymer |
JP2002338918A (en) * | 2001-05-22 | 2002-11-27 | Sekisui Chem Co Ltd | Surface protection film |
JP2005290315A (en) * | 2004-04-05 | 2005-10-20 | Kotou Kogyo Kk | Pressure-sensitive adhesive tape for curing coating |
JP2008208173A (en) | 2007-02-23 | 2008-09-11 | Nitto Denko Corp | Surface protecting sheet |
JP5466852B2 (en) | 2008-12-01 | 2014-04-09 | 出光ユニテック株式会社 | Surface protection film |
JP5682011B2 (en) | 2010-03-31 | 2015-03-11 | 東レフィルム加工株式会社 | Surface protection film |
US20130149525A1 (en) | 2010-03-31 | 2013-06-13 | Toray Advanced Film Co., Ltd. | Surface protection film |
CN105793372B (en) | 2013-11-21 | 2019-07-23 | 株式会社可乐丽 | Surface protective film |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4163077A (en) * | 1978-04-19 | 1979-07-31 | Minnesota Mining And Manufacturing Company | Contamination-tolerant pressure-sensitive adhesive tape |
-
1984
- 1984-10-27 JP JP59226463A patent/JPH07116410B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9873788B2 (en) | 2014-04-08 | 2018-01-23 | Asahi Kasei Kabushiki Kaisha | Composition and surface protection film |
Also Published As
Publication number | Publication date |
---|---|
JPS61103975A (en) | 1986-05-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |