JPH07188620A - Film for surface protection - Google Patents
Film for surface protectionInfo
- Publication number
- JPH07188620A JPH07188620A JP33324393A JP33324393A JPH07188620A JP H07188620 A JPH07188620 A JP H07188620A JP 33324393 A JP33324393 A JP 33324393A JP 33324393 A JP33324393 A JP 33324393A JP H07188620 A JPH07188620 A JP H07188620A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- film
- pressure
- 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
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、塗装を施した鋼板、合
成樹脂成形品、あるいは、自動車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 a coated steel plate, a synthetic resin molded product, or an automobile.
【0002】[0002]
【従来の技術】従来より、塗装を施した鋼板、ステンレ
ス板、アルミサッシ板、機械部品、金属製家庭用品、合
成樹脂成形品等の汚染や外傷を防止する為に(1)ポリ
エステル樹脂、塩化ビニル樹脂、ポリエチレン樹脂等の
基材に再剥離性を有するゴム系、アクリル系等の粘着剤
を塗布した積層体や、(2)ポリオレフィン系樹脂に酸
化チタン等の無機系微粒子を0.1〜10重量%添加し
て波長300〜360nmの紫外線透過率を10%以下
にしたポリオレフィン系樹脂フィルムに感圧性粘着剤を
塗布してなる表面保護用粘着テープ(特開平4−153
287)等が提案されている。2. Description of the Related Art Conventionally, in order to prevent contamination and external damage of painted steel plates, stainless steel plates, aluminum sash plates, machine parts, metal household products, synthetic resin molded products, etc. (1) Polyester resin, chloride A laminate in which a base material such as vinyl resin or polyethylene resin is coated with a releasable rubber-based or acrylic-based pressure-sensitive adhesive, or (2) a polyolefin-based resin containing 0.1 to 5 inorganic fine particles such as titanium oxide. Adhesive tape for surface protection, which is obtained by applying a pressure-sensitive adhesive to a polyolefin resin film having 10% by weight of ultraviolet ray transmittance of 10% or less at a wavelength of 300 to 360 nm (JP-A-4-153).
287) and the like have been proposed.
【0003】しかし、塗装鋼板、合成樹脂成形品及び輸
出用自動車等は需要者の手にわたるまでに、屋外に数ケ
月〜1年にわたって一時保管される場合があり、このよ
うな場合には、(1)のような積層体を表面保護フィル
ムとして使用すると、一時保管の間に密着した部分とそ
うでない部分(気泡の入った部分)とで、塗面状態に差
が生じ、表面保護フィルムを剥がした後に光沢の異なる
模様となって現れるという問題を有している。又、
(2)の粘着テープを使用した場合には、紫外線および
可視光線の遮蔽が不十分で、粘着剤の熱劣化等がおこ
り、粘着テープを剥離した後の被着体の塗装表面に粘着
剤が糊残りするという問題があった。この(2)の場
合、無機系微粒子の添加量を増せば紫外線等の遮蔽性は
改善されるが、逆に微粒子が表面にブリードすることに
よる汚染等の新たな問題を生ずる。However, coated steel sheets, synthetic resin molded products, automobiles for export, etc. may be temporarily stored outdoors for several months to a year before reaching the demand of consumers. In such a case, ( When a laminate such as 1) is used as a surface protection film, a difference occurs in the coating surface state between the part that is not in close contact and the part that is not (the part containing air bubbles) during temporary storage, and the surface protection film is peeled off. After that, it has a problem that it appears as a pattern with different gloss. or,
When the pressure-sensitive adhesive tape of (2) is used, the ultraviolet rays and visible rays are not sufficiently shielded, heat deterioration of the pressure-sensitive adhesive occurs, and the pressure-sensitive adhesive remains on the coated surface of the adherend after peeling the pressure-sensitive adhesive tape. There was a problem of adhesive residue. In the case of this (2), the shielding property against ultraviolet rays and the like is improved by increasing the addition amount of the inorganic fine particles, but on the contrary, a new problem such as contamination due to bleeding of the fine particles on the surface occurs.
【0004】[0004]
【発明が解決しようとする課題】屋外に長期間放置され
ても、基材および粘着剤の劣化がなく、被着体の塗装表
面に影響を及ぼすこともなく、また、配合剤がブリード
アウトすることもない表面保護フィルムの提供。Even when left outdoors for a long period of time, the base material and the adhesive are not deteriorated, the coated surface of the adherend is not affected, and the compounding agent bleeds out. Providing a surface protection film that never happens.
【0005】[0005]
【課題を解決するための手段】本発明者等は、ポリオレ
フィン系樹脂に特定量の酸化チタンおよび紫外線吸収剤
を配合することにより、上記課題を解決できることを見
出し、本発明を完成した。即ち、本発明の要旨とすると
ころは、ポリオレフィン系樹脂100重量部に酸化チタ
ン10〜30重量部及び紫外線吸収剤0.1〜5重量部
を配合し製膜してなるポリオレフィン系樹脂基材層の片
面に、粘着剤層が形成されてなることを特徴とする表面
保護フィルム、に存する。The present inventors have completed the present invention by finding that the above problems can be solved by blending a specific amount of titanium oxide and an ultraviolet absorber in a polyolefin resin. That is, the gist of the present invention is that a polyolefin-based resin base layer formed by mixing 10 to 30 parts by weight of titanium oxide and 0.1 to 5 parts by weight of an ultraviolet absorber with 100 parts by weight of a polyolefin-based resin to form a film. And a pressure-sensitive adhesive layer formed on one surface thereof.
【0006】以下、本発明について詳述する。本発明に
おいて用いられるポリオレフィン系樹脂としては、ポリ
エチレン、ポリプロピレン、ポリエチレン・ポリプロピ
レンブロックコポリマー、エチレン・酢酸ビニル共重合
体またはこれらの混合物等が挙げられる。酸化チタンと
しては、ルチル型酸化チタンがそれ自体の耐候性がよい
ので好ましく、酸化チタンは、ポリオレフィン系樹脂1
00重量部に対して10〜30重量部好ましくは10〜
20重量部配合する。酸化チタンが10重量部より少な
いと、紫外線及び/または可視光線の遮蔽が十分でな
く、粘着剤の劣化がおこり、表面保護フィルム(以下、
「フィルム」という)の再剥離性、フィルム剥離後の塗
装表面汚染防止性が劣り、30重量部より多いと酸化チ
タンがブリードアウトし、フィルムの初期粘着力が低下
し、また、剥離後の塗装表面汚染防止性も劣る。The present invention will be described in detail below. Examples of the polyolefin resin used in the present invention include polyethylene, polypropylene, polyethylene / polypropylene block copolymers, ethylene / vinyl acetate copolymers, and mixtures thereof. As the titanium oxide, rutile type titanium oxide is preferable because it has good weather resistance, and the titanium oxide is preferably the polyolefin resin 1
10 to 30 parts by weight, preferably 10 to 100 parts by weight
Add 20 parts by weight. If the amount of titanium oxide is less than 10 parts by weight, the ultraviolet and / or visible light is not sufficiently shielded, and the pressure-sensitive adhesive is deteriorated.
Removability of "(film)" and coating surface contamination prevention property after film peeling are inferior, and when it is more than 30 parts by weight, titanium oxide bleeds out, the initial adhesive strength of the film decreases, and coating after peeling The surface contamination preventive property is also inferior.
【0007】紫外線吸収剤としては、波長290〜38
0nmに吸収極大のあるものであればいずれでもよく、
従来公知の紫外線吸収剤、例えば、2−ヒドロキシ−4
−メトキシベンゾフェノン、2−ヒドロキシ−4−n−
オクチルオキシベンゾフェノン、2−ヒドロキシ−4−
n−ドデシルオキシベンゾフェノン、2,2’,4,
4’−テトラヒドロキシベンゾフェノン等のベンゾフェ
ノン系紫外線吸収剤;2−(2’−ヒドロキシ−3’−
メチルフェニル)ベンゾトリアゾール、2−(2’−ヒ
ドロキシ−3’−tert−ブチルフェニル)ベンゾト
リアゾール、2−(2’−ヒドロキシ−3’,5’−ジ
−tert−ブチルフェニル)−5−クロロベンゾトリ
アゾール、2−(2’−ヒドロキシ−3’−tert−
ブチル−5’−メチルフェニル)−5−クロロベンゾト
リアゾール、2−(2’−ヒドロキシ−3’−メチルフ
ェニル)−5−ブトキシカルボニルベンゾトリアゾール
等のベンゾトリアゾール系紫外線吸収剤;フェニルサリ
シレート、p−tert−ブチルフェニルサリシレー
ト、p−メチルフェニルサリシレート、p−オクチルフ
ェニルサリシレート等のサリチル酸エステル系紫外線吸
収剤等が挙げられるが、ポリオレフィン系樹脂と相溶性
が良く塗装鋼板等への汚染性が少ないという点からベン
ゾフェノン系紫外線吸収剤が好ましい。紫外線吸収剤
は、ポリオレフィン系樹脂100重量部に対して0.1
〜5重量部好ましくは0.2〜3重量部配合する。The ultraviolet absorber has a wavelength of 290 to 38.
Any one having an absorption maximum at 0 nm may be used,
Conventionally known ultraviolet absorbers such as 2-hydroxy-4
-Methoxybenzophenone, 2-hydroxy-4-n-
Octyloxybenzophenone, 2-hydroxy-4-
n-dodecyloxybenzophenone, 2,2 ', 4
Benzophenone-based UV absorbers such as 4'-tetrahydroxybenzophenone; 2- (2'-hydroxy-3'-
Methylphenyl) benzotriazole, 2- (2'-hydroxy-3'-tert-butylphenyl) benzotriazole, 2- (2'-hydroxy-3 ', 5'-di-tert-butylphenyl) -5-chloro Benzotriazole, 2- (2'-hydroxy-3'-tert-
Butyl-5'-methylphenyl) -5-chlorobenzotriazole, 2- (2'-hydroxy-3'-methylphenyl) -5-butoxycarbonylbenzotriazole and other benzotriazole ultraviolet absorbers; phenyl salicylate, p- Examples include salicylic acid ester-based UV absorbers such as tert-butylphenyl salicylate, p-methylphenyl salicylate, and p-octylphenyl salicylate, but they have good compatibility with polyolefin-based resins and little pollution to coated steel sheets. Therefore, a benzophenone type ultraviolet absorber is preferable. The ultraviolet absorber is 0.1 per 100 parts by weight of the polyolefin resin.
-5 parts by weight, preferably 0.2-3 parts by weight.
【0008】紫外線吸収剤が0.1重量部より少ない場
合には紫外線の遮蔽が十分でなく、粘着剤の劣化等が起
こり、フィルムの再剥離性、剥離後の塗装表面汚染防止
性が劣る。また5重量部より多いと紫外線吸収剤がブリ
ードアウトする恐れがある。酸化チタンと紫外線吸収剤
の両者あるいは片方が配合されていなかったり、所定の
配合量に満たなかった場合、耐候性が十分でなくなり、
屋外使用後表面保護フィルムを剥がした際、劣化した粘
着剤が塗装鋼板等に残る恐れがある。また、所定の配合
量を超えた場合、フィルムを剥がした際、塗装鋼板等が
汚染されていて、光沢が落ちるという問題がある。When the amount of the ultraviolet absorber is less than 0.1 parts by weight, the ultraviolet ray is not sufficiently shielded, the adhesive is deteriorated, and the removability of the film and the prevention of the coating surface contamination after the peeling are deteriorated. If it is more than 5 parts by weight, the ultraviolet absorbent may bleed out. If both or one of the titanium oxide and the ultraviolet absorber is not blended or if the prescribed blending amount is not met, the weather resistance becomes insufficient,
When the surface protective film is peeled off after outdoor use, the deteriorated adhesive may remain on the coated steel plate or the like. Further, when the content exceeds a predetermined amount, there is a problem that when the film is peeled off, the coated steel sheet and the like are contaminated and the gloss is reduced.
【0009】ポリオレフィン系樹脂に上記した酸化チタ
ン及び紫外線吸収剤を配合した後、従来公知の方法、例
えばTダイ及びインフレーション装置等の通常使用され
る押出し機により成膜し、ポリオレフィン系樹脂基材層
(以下、「基材層」という)とする。基材層の厚さは、
配合物、用途に応じて適宜決めればよいが、通常20〜
150μm程度とする。厚さが20μm未満では外傷に
対する抵抗力に劣る場合があり、また、150μmを超
えるとラッピング性に劣る場合や、経済性にも劣る場合
があるので好ましくない。After blending the above-mentioned titanium oxide and ultraviolet absorber with a polyolefin resin, a film is formed by a conventionally known method, for example, a commonly used extruder such as a T-die and an inflation device, and a polyolefin resin substrate layer. (Hereinafter referred to as "base material layer"). The thickness of the base material layer is
It may be appropriately determined depending on the compound and the use, but usually 20 to
It is about 150 μm. If the thickness is less than 20 μm, the resistance to external damage may be poor, and if it exceeds 150 μm, the lapping property may be poor or the economy may be poor, which is not preferable.
【0010】本発明の基材層の光線透過率は、紫外部
(300〜360nm)の透過率が5%以下となるもの
であり、好ましくは2%以下、特に好ましくは1%以下
となるのが良く、また、可視部(400〜700nm)
の透過率は50%以下となるものであり、好ましくは3
0%以下、更に好ましくは20%以下が良い。The light transmittance of the base material layer of the present invention is such that the ultraviolet (300 to 360 nm) transmittance is 5% or less, preferably 2% or less, particularly preferably 1% or less. Good, and visible part (400-700nm)
Has a transmittance of 50% or less, preferably 3
It is preferably 0% or less, more preferably 20% or less.
【0011】本発明において用いる粘着剤としては、再
剥離性がよく、糊残りもしにくいという点で、ゴム系粘
着剤が好ましく、天然ゴム系、合成ゴム系糊着剤が使用
できる。合成ゴム系粘着剤としては、イソブチレン−イ
ソプレン共重合体やポリイソブチレンよりなる粘着剤が
挙げられる。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液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層上に塗布
し、乾燥すればよい。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、光安定剤、ブロッキング防止剤、滑剤等の添加剤を
配合することができる。The pressure-sensitive adhesive used in the present invention is preferably a rubber-based pressure-sensitive adhesive because it has good removability and is less likely to leave an adhesive residue, and natural rubber-based or synthetic rubber-based adhesives can be used. Examples of the synthetic rubber-based pressure-sensitive adhesive include pressure-sensitive adhesives made of isobutylene-isoprene copolymer and polyisobutylene. To form a pressure-sensitive adhesive layer on the base material layer, a coating solution prepared by dissolving the pressure-sensitive adhesive in a soluble solvent such as toluene is applied on the base material layer by a usual method such as a reverse coating method and dried. do it. In addition, known additives such as antioxidants, light stabilizers, antiblocking agents, and lubricants can 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.
【0012】[0012]
【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.
【0013】実施例1 ポリプロピレン(三菱化成(株)製、PF341)10
0重量部に酸化チタン(石原産業(株)製、R−83
0)15重量部、紫外線吸収剤(ベンゾフェノン系、ア
メリカンシアナミド社製、UV−531)1重量部を配
合してなる樹脂組成物をTダイ法にて厚さ50μmのフ
ィルムになるように成膜し、基材層フィルムとした。こ
の基材層フィルムにブチルゴム粘着剤(エクソン化学
(株)製、IIR:100重量部、ビスタネックスL
M:50重量部、トルエン450重量部からなる)をリ
バースコート法により、乾燥後10μm厚になるように
塗布し、表面保護フィルムを得た。 Example 1 Polypropylene (PF341, manufactured by Mitsubishi Kasei Co., Ltd.) 10
0 parts by weight of titanium oxide (R-83 manufactured by Ishihara Sangyo Co., Ltd.)
0) 15 parts by weight and 1 part by weight of an ultraviolet absorber (benzophenone-based, American Cyanamide, UV-531) are mixed to form a film having a thickness of 50 μm by a T-die method. Then, a substrate layer film was obtained. Butyl rubber adhesive (manufactured by Exxon Chemical Co., Ltd., IIR: 100 parts by weight, Vistanex L)
(M: 50 parts by weight, toluene: 450 parts by weight) was applied by a reverse coating method to a thickness of 10 μm after drying to obtain a surface protective film.
【0014】実施例2 ポリプロピレン(PF341)90重量部、低密度ポリ
エチレン(三菱化成(株)製、F141)10重量部に
酸化チタン(R−830)18重量部、紫外線吸収剤
(UV−531)0.6重量部を配合してなる樹脂組成
物をTダイ法にて厚さ40μmのフィルムになるように
成膜し、基材層フィルムとした。この基材層フィルムに
ポリイソブチレン粘着剤(トーネックス社製、LM−M
H−LC:100重量部とエクソン化学(株)製、ビス
タネックスLM:50重量部、トルエン450重量部か
らなる)をリバースコート法により、乾燥後15μm厚
になるように塗布し、表面保護フィルムを得た。 Example 2 90 parts by weight of polypropylene (PF341), 10 parts by weight of low-density polyethylene (F141 manufactured by Mitsubishi Kasei Co., Ltd.), 18 parts by weight of titanium oxide (R-830), and an ultraviolet absorber (UV-531). A resin composition containing 0.6 part by weight was formed into a film having a thickness of 40 μm by a T-die method to obtain a substrate layer film. A polyisobutylene adhesive (LM-M manufactured by Tonex Co., Ltd.) is added to the base layer film.
H-LC: 100 parts by weight and Exxon Chemical Co., Ltd., Vistanex LM: 50 parts by weight and toluene 450 parts by weight) are applied by a reverse coating method to a thickness of 15 μm after drying, and a surface protective film Got
【0015】比較例1〜6 実施例1において、酸化チタン(R−830)と紫外線
吸収剤(UV−531)を表−1に示した配合量とする
以外は実施例1と同様にして、表面保護フィルムを得
た。 Comparative Examples 1 to 6 In the same manner as in Example 1, except that the amounts of titanium oxide (R-830) and ultraviolet absorber (UV-531) used in Example 1 were changed to those shown in Table 1. A surface protection film was obtained.
【0016】比較例7 実施例1と同様にして基材層フィルムを成膜し、これに
アクリル系粘着剤(綜研化学社製、SKダイン1491
H)を乾燥後10μm厚になるように塗布し、表面保護
フィルムを得た。 Comparative Example 7 A substrate layer film was formed in the same manner as in Example 1, and an acrylic pressure-sensitive adhesive (SK Dyne 1491, manufactured by Soken Chemical Co., Ltd.) was formed thereon.
H) was dried and then applied to a thickness of 10 μm to obtain a surface protective film.
【0017】上記実施例および比較例で得た基材層フィ
ルムの(平均)光線透過率を測定し、表面保護フィルム
については初期粘着力、再剥離性及び剥離後の塗装表面
汚染防止性を評価し、結果を表−2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。 (2)再剥離性及び剥離後の塗装表面汚染防止性 表面保護フィルムを塗装鋼板に貼り付け、屋外に6ケ月
間さらした後、フィルムを剥がし、その時の再剥離性及
び塗装表面への汚染防止性を評価した。評価基準は次の
通りである。The (average) light transmittances of the substrate layer films obtained in the above Examples and Comparative Examples were measured, and the surface protective films were evaluated for initial adhesive strength, removability and paint surface contamination prevention after peeling. The results are shown in Table-2. 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. (2) Removability and prevention of paint surface contamination after peeling A surface protective film is attached to a coated steel sheet and exposed outdoors for 6 months, then the film is peeled off, and removability at that time and prevention of contamination on the coated surface The sex was evaluated. The evaluation criteria are as follows.
【0018】再剥離性 ○・・・良好(粘着剤残りなし) △・・・わずかに粘着剤残り有り ×・・・粘着剤残り大 塗装表面汚染防止性 ○・・・良好(外観変化なし) △・・・微少な外観変化有り ×・・・著しい外観変化有り −・・・粘着剤残りのため評価できずRemovability ○ ・ ・ ・ Good (no adhesive residue left) △ ・ ・ ・ Slight adhesive residue left × ・ ・ ・ A large amount of adhesive residue Paint surface contamination prevention property ○ ・ ・ ・ Good (no change in appearance) △: Minor change in appearance ×: Significant change in appearance --- Unable to evaluate due to residual adhesive
【0019】[0019]
【発明の効果】本発明の表面保護フィルムは、初期粘着
力、再剥離性に優れ、また、長期間屋外に放置されて
も、被着体の塗装表面を汚染することなく、塗装を施し
た鋼板、合成樹脂成形品、あるいは自動車等の表面保護
フィルムとして極めて有用であるEFFECTS OF THE INVENTION The surface protective film of the present invention is excellent in initial adhesive strength and removability, and is coated without contaminating the coated surface of the adherend even when it is left outdoors for a long time. Extremely useful as a steel plate, synthetic resin molded product, or surface protection film for automobiles, etc.
【0020】[0020]
【表1】 [Table 1]
【0021】[0021]
【表2】 [Table 2]
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B32B 27/32 Z 8115−4F // C08K 3/22 C08L 23/02 KEC ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location B32B 27/32 Z 8115-4F // C08K 3/22 C08L 23/02 KEC
Claims (2)
化チタン10〜30重量部及び紫外線吸収剤0.1〜5
重量部を配合し製膜してなるポリオレフィン系樹脂基材
層の片面に、粘着剤層が形成されてなることを特徴とす
る表面保護フィルム。1. A polyolefin resin of 100 parts by weight, titanium oxide of 10 to 30 parts by weight, and an ultraviolet absorber of 0.1 to 5 parts by weight.
A surface protection film comprising a pressure-sensitive adhesive layer formed on one surface of a polyolefin-based resin base material layer prepared by blending parts by weight.
載の表面保護フィルム。2. The surface protective film according to claim 1, wherein the adhesive is a rubber-based adhesive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33324393A JPH07188620A (en) | 1993-12-27 | 1993-12-27 | Film for surface protection |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33324393A JPH07188620A (en) | 1993-12-27 | 1993-12-27 | Film for surface protection |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07188620A true JPH07188620A (en) | 1995-07-25 |
Family
ID=18263930
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33324393A Pending JPH07188620A (en) | 1993-12-27 | 1993-12-27 | Film for surface protection |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07188620A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004529007A (en) * | 2001-04-10 | 2004-09-24 | バイエル アクチェンゲゼルシャフト | Heat absorbing coating system |
KR100593564B1 (en) * | 1997-09-27 | 2006-08-30 | 테사 악티엔게젤샤프트 | Self-adhesive protective film with olefin rubber adhesive |
JP2008030462A (en) * | 2006-06-28 | 2008-02-14 | Toray Pef Products Inc | Weather resistant polyolefin resin laminated foam |
-
1993
- 1993-12-27 JP JP33324393A patent/JPH07188620A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100593564B1 (en) * | 1997-09-27 | 2006-08-30 | 테사 악티엔게젤샤프트 | Self-adhesive protective film with olefin rubber adhesive |
JP2004529007A (en) * | 2001-04-10 | 2004-09-24 | バイエル アクチェンゲゼルシャフト | Heat absorbing coating system |
JP2008030462A (en) * | 2006-06-28 | 2008-02-14 | Toray Pef Products Inc | Weather resistant polyolefin resin laminated foam |
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