JPH02142877A - Polyvinyl chloride resin self-adhesive film - Google Patents

Polyvinyl chloride resin self-adhesive film

Info

Publication number
JPH02142877A
JPH02142877A JP29703488A JP29703488A JPH02142877A JP H02142877 A JPH02142877 A JP H02142877A JP 29703488 A JP29703488 A JP 29703488A JP 29703488 A JP29703488 A JP 29703488A JP H02142877 A JPH02142877 A JP H02142877A
Authority
JP
Japan
Prior art keywords
film
chloride resin
vinyl chloride
polyvinyl chloride
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.)
Granted
Application number
JP29703488A
Other languages
Japanese (ja)
Other versions
JP2587280B2 (en
Inventor
Kazuo Tanaka
一雄 田中
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.)
Bando Chemical Industries Ltd
Original Assignee
Bando Chemical Industries 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 Bando Chemical Industries Ltd filed Critical Bando Chemical Industries Ltd
Priority to JP29703488A priority Critical patent/JP2587280B2/en
Publication of JPH02142877A publication Critical patent/JPH02142877A/en
Application granted granted Critical
Publication of JP2587280B2 publication Critical patent/JP2587280B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the title film prevented from plasticizer migration to the self-adhesive layer and from decreasing in adhesive force with the lapse of time without detriment to the printability, heat resistance, weathering resistance, etc., by forming an acryl self-adhesive layer on a specified vinyl chloride resin film. CONSTITUTION:100 pts.wt. vinyl chloride polymer comprising vinyl chloride and at most 20wt.% other monomers is mixed with 10-45 pts.wt. liquid plasticizer (e.g., dioctyl adipate) and 0.1-5.0 pts.wt. hydrotalcite compound, and the mixture is molded into a film to obtain a vinyl chloride resin film. An acrylic self-adhesive is applied to this film and dried.

Description

【発明の詳細な説明】 崖1」JIり肥別黙 本発明は、半硬質ポリ塩化ビニル系樹脂粘着フィルムに
関し、詳しくは、種々のマーキングフィルム、マスキン
グテープ、保護フィルム等に適する半硬質ポリ塩化ビニ
ル系樹脂粘着フィルムであって、経時的に粘着力の低下
のない半硬質ポリ塩化ビニル系樹脂粘着フィルムに関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a semi-rigid polyvinyl chloride resin adhesive film, and more specifically, a semi-rigid polyvinyl chloride adhesive film suitable for various marking films, masking tapes, protective films, etc. This invention relates to a semi-rigid polyvinyl chloride resin adhesive film that does not lose its adhesive strength over time.

従来■吸血 看板、ウィンドー・デイスプレィ、車両、各種塔槽類、
配管、プラント機器等に用いられるマーキングフィルム
、自動車や各種機器類の塗装置1.’lに非塗装領域に
貼着されるマスキングテープ、各種基材の表面保護に用
いられる保護フィルム等は、多くは、液状の可塑剤を含
有する半硬質塩化ビニル系樹脂からなるフィルムにアク
リル系粘着剤層を設けて形成されている。
Conventional ■ Vampire signs, window displays, vehicles, various towers and tanks,
Marking film used for piping, plant equipment, etc., coating equipment for automobiles and various equipment 1. Masking tapes that are applied to non-painted areas, protective films that are used to protect the surface of various base materials, etc. are often made of semi-rigid vinyl chloride resin containing liquid plasticizer and acrylic. It is formed with an adhesive layer.

しかし、かかる従来のポリ塩化ビニル系樹脂粘着フィル
ムにおいては、フィルムに含有される液状可塑剤が粘着
剤層に移行して、粘着力が経時的に大幅に低下する。
However, in such conventional polyvinyl chloride resin adhesive films, the liquid plasticizer contained in the film migrates to the adhesive layer, resulting in a significant decrease in adhesive strength over time.

このような問題を解決するために、従来、例えば、フィ
ルムに予めプライマー処理を施した後、これにアクリル
系粘着剤層を設ける方法が提案されているが、製造工程
数を増加させ、製造費用を高くする。また、特開昭60
−4543号公報や特開昭60−195146号公報、
特開昭60195147号公報等に記載されているよう
に、ポリ塩化ビニルに液状可塑剤と共に、低分子量のア
クリル樹脂や、或いはエチレン/酢酸ビニル共重合体、
エチレン/酢酸ビニル/−酸化炭素共重合体等を加える
等の方法も擢案されているが、上記の方法と同様に、製
造費用を高くするほか、粘着力の経時低下を十分に抑え
ることができない。
In order to solve these problems, a method has been proposed in the past, for example, to apply a primer treatment to the film and then apply an acrylic adhesive layer thereon. However, this method increases the number of manufacturing steps and increases the manufacturing cost. make it higher. Also, JP-A-60
-4543 publication and JP-A-60-195146 publication,
As described in JP-A-60195147, etc., polyvinyl chloride is combined with a liquid plasticizer, a low molecular weight acrylic resin, or an ethylene/vinyl acetate copolymer.
Methods such as adding ethylene/vinyl acetate/-carbon oxide copolymer have also been proposed, but like the above method, they increase production costs and are difficult to sufficiently suppress the decline in adhesive strength over time. Can not.

が ′ しようとする課 本発明者は、従来のアクリル系粘着剤層を有する半硬質
ポリ塩化ビニル系樹脂粘着フィルムにおける上記した問
題を解決するために鋭意研究した結果、基材半硬質ポリ
塩化ビニル系樹脂フィルムに所定量のハイドロタルサイ
)l化合物を配合することによって、マーキングフィル
ム、マスキングテープ、保護フィルム等に要求される印
刷性、耐熱性、耐候性等を低下させることなく、十記可
塑剤の粘着剤層の移行を防止して、粘着力の経時低下を
よく抑えることができることを見出して、本発明に至っ
たものである。
As a result of intensive research to solve the above-mentioned problems in conventional semi-rigid polyvinyl chloride resin adhesive films having an acrylic adhesive layer, the present inventors discovered that the semi-rigid polyvinyl chloride base material By blending a predetermined amount of hydrotalcyl compound into a resin film, it is possible to improve the properties of the above plasticizers without reducing the printability, heat resistance, weather resistance, etc. required for marking films, masking tapes, protective films, etc. The present invention was developed based on the discovery that it is possible to effectively suppress the deterioration of adhesive strength over time by preventing migration of the adhesive layer.

従って、本発明は、経時的に粘着力の低下のない半硬質
ポリ塩化ビニル系樹脂粘着フィルムを提供することを目
的とする。
Therefore, an object of the present invention is to provide a semi-rigid polyvinyl chloride resin adhesive film that does not lose its adhesive strength over time.

課題)邂訣するためq1段 本発明による半硬質ポリ塩化ビニル系樹脂粘着フィルム
は、塩化ビニル系重合体100重量部について、液状可
塑剤を10〜45重量部とノ\イトロタルサイト類化合
物を0.1〜5重量部含有する塩化ビニル系樹脂からな
るフィルムにアクリル系粘着剤層を設けてなることを特
徴とする。
The semi-rigid polyvinyl chloride resin adhesive film according to the present invention is prepared by adding 10 to 45 parts by weight of a liquid plasticizer and a notrotalcite compound to 100 parts by weight of a vinyl chloride polymer. It is characterized by being formed by providing an acrylic adhesive layer on a film made of a vinyl chloride resin containing 0.1 to 5 parts by weight.

本発明において、塩化ビニル系重合体とは、塩化ビニル
の単独重合体のほか、塩化ビニルと種々の単量体との共
重合体を含むものとする。かかる共単量体としては、例
えば、エチレン、プロピレン、ブチレン等のα−オレフ
ィン、フッ化ビニル、塩化ビニリデン等の塩化ビニル以
外のハロゲン化ビニル及びハロゲン化ビニリデン、酢酸
ビニル、プロピオン酸ビニル等のビニルエステル等の1
種又は2種以上を挙げることができる。これら共単量体
は、塩化ビニル共重合体において、通常、20重量%以
下であることが好ましい。
In the present invention, the vinyl chloride polymer includes not only vinyl chloride homopolymers but also copolymers of vinyl chloride and various monomers. Examples of such comonomers include α-olefins such as ethylene, propylene, and butylene, vinyl halides other than vinyl chloride such as vinyl fluoride and vinylidene chloride, and vinyl such as vinylidene halides, vinyl acetate, and vinyl propionate. 1 of ester etc.
A species or two or more species may be mentioned. The content of these comonomers in the vinyl chloride copolymer is usually preferably 20% by weight or less.

本発明において用いる基材である半硬質ポリ塩化ビニル
系樹脂は、液状可塑剤を含有する。かかる液状可塑剤と
しては、エステル系可塑剤が好ましく、特に、例えば、
ジオクチルアジペート、ジオクチルフタレート等のフタ
ル酸ジエステル系可塑剤や、ポリエステル系可塑剤が好
適に用いられる。ポリエステル系可塑剤は、よく知られ
ているように、マレイン酸、アジピン酸、フタル酸、ア
ゼライン酸、セバシン酸等の二塩基酸と、エチレングリ
コール、1.2−プロピレングリコール、13−ブチレ
ングリコール、1,4−ブタンジオール、ネオペンチル
グリコール、ジプロピレングリコール、1,6−ヘキサ
ンジオール等のグリコールとをn−オクチルアルコール
、n−デシルアルコール等の適宜の停止剤の存在下に反
応させて得られる可塑剤である。
The semi-rigid polyvinyl chloride resin that is the base material used in the present invention contains a liquid plasticizer. As such liquid plasticizers, ester plasticizers are preferable, and in particular, for example,
Phthalate diester plasticizers such as dioctyl adipate and dioctyl phthalate, and polyester plasticizers are preferably used. As is well known, polyester plasticizers include dibasic acids such as maleic acid, adipic acid, phthalic acid, azelaic acid, and sebacic acid, and ethylene glycol, 1,2-propylene glycol, 13-butylene glycol, Obtained by reacting glycols such as 1,4-butanediol, neopentyl glycol, dipropylene glycol, and 1,6-hexanediol in the presence of an appropriate terminator such as n-octyl alcohol or n-decyl alcohol. It is a plasticizer.

また、上記以外にも、例えば、ジ−n−ブチルアジペー
ト、ジ(2−エチルへキシル)アジペート、ジイソデシ
ルアジペート等のアジピン酸ジアルキルエステル、トリ
 (2−エチルへキシル)トリメリテート、トリ (n
−オクチル)トリメリテート、トリ (イソデシル)ト
リメリテート等のトリメリド酸トリアルキルエステル等
も用いられる。
In addition to the above, examples include adipic acid dialkyl esters such as di-n-butyl adipate, di(2-ethylhexyl) adipate, and diisodecyl adipate, tri(2-ethylhexyl) trimellitate, tri(n
Trimelidic acid trialkyl esters such as -octyl) trimellitate and tri(isodecyl) trimellitate are also used.

かかる液状可塑剤は、塩化ビニル系重合体100重量部
について、10〜45重量部の範囲で配合される。液状
可塑剤の配合量が塩化ビニル系重合体100重量部につ
いて、10重量部よりも少ないときは、得られるフィル
ムの剛性が大きく、伸びが小さいために、前記した用途
に用いるに適さない。しかし、45重量部を耐えるとき
は、得られるフィルムが過度に柔軟であって、所謂腰が
ないので、同様に、前記した用途に用いるに適さない。
Such a liquid plasticizer is blended in an amount of 10 to 45 parts by weight per 100 parts by weight of the vinyl chloride polymer. If the amount of liquid plasticizer is less than 10 parts by weight per 100 parts by weight of the vinyl chloride polymer, the resulting film will have high rigidity and low elongation, making it unsuitable for use in the above-mentioned applications. However, when it withstands 45 parts by weight, the resulting film is too flexible and has no stiffness, and is therefore similarly unsuitable for the above-mentioned applications.

本発明によれば、基材である半硬質ポリ塩化ビニル系樹
脂は、更に、ハイドロタルサイト類化合物を含有する。
According to the present invention, the semi-rigid polyvinyl chloride resin that is the base material further contains a hydrotalcite compound.

かかるハイドロタルサイl−類化合物は、合成品が、例
えば、協和化学工業−から1アルカマイザー■」やrD
HT−4AJとして市販されており、本発明においては
、かかる市販品を好適に用いることができる。
Such hydrotalcium-1-class compounds are synthesized by, for example, Kyowa Kagaku Kogyo's 1 Alkamizer ■ and rD.
It is commercially available as HT-4AJ, and such a commercial product can be suitably used in the present invention.

かかるハイドロタルサイト類化合物は、塩化ビニル系重
合体100重量部について、0.1〜5.0重量部の範
囲で配合される。ハイドロタルサイト類化合物の配合量
が塩化ビニル系重合体100重量部について、0.1重
量部よりも少ないときは、目的とする粘着フィルムの粘
着力の経時低下を十分に抑えることができず、他方、5
.0重量部を越えるときは、得られるフィルムの伸びの
低下が著しく、前記した用途への使用に適さない。
The hydrotalcite compound is blended in an amount of 0.1 to 5.0 parts by weight based on 100 parts by weight of the vinyl chloride polymer. When the amount of the hydrotalcite compound is less than 0.1 part by weight per 100 parts by weight of the vinyl chloride polymer, it is not possible to sufficiently suppress the deterioration of the adhesive strength of the desired adhesive film over time. On the other hand, 5
.. When the amount exceeds 0 parts by weight, the elongation of the resulting film is significantly reduced, making it unsuitable for use in the above-mentioned applications.

本発明においては、基材である半硬質ポリ塩化ビニル系
樹脂は、更に、必要に応じて、安定剤、滑剤、充填剤、
着色剤、加工助剤、軟化剤、金属粉、防曇剤、紫外線吸
収剤、酸化防止剤、帯電防止剤、難燃剤等を適宜に含有
していてもよい。安定剤としては、例えば、Ba−Zn
系、Cd −Ba系、Sn系等のものが用いられ、或い
はこれらがエポキシ化人豆油、エポキシ樹脂等と併用さ
れる。また、軟化剤としては、例えば、エチレン/酢酸
ビニル共重合体やエチレン/酢酸ビニル/−酸化炭素共
重合体等が用いられる。
In the present invention, the semi-rigid polyvinyl chloride resin that is the base material may further contain stabilizers, lubricants, fillers,
It may contain a colorant, a processing aid, a softener, a metal powder, an antifogging agent, an ultraviolet absorber, an antioxidant, an antistatic agent, a flame retardant, etc. as appropriate. As the stabilizer, for example, Ba-Zn
epoxidized human bean oil, epoxy resin, etc. are used. Further, as the softening agent, for example, ethylene/vinyl acetate copolymer, ethylene/vinyl acetate/-carbon oxide copolymer, etc. are used.

上記したような基材半硬質ポリ塩化ビニル系樹脂フィル
ムは、カレンダー加工、押出加工、キャスト加工等によ
ってフィルムに加工することができる。かかるフィルム
にアクリル系粘着剤を塗布し、乾燥すれば、本発明によ
るポリ塩化ビニル系樹脂粘着フィルムを得ることができ
る。アクリル系粘着剤は、従来よりポリ塩化ビニル系樹
脂粘着フィルムに用いられている通常の粘着剤を用いる
ことができる。
The base semi-rigid polyvinyl chloride resin film as described above can be processed into a film by calendering, extrusion, casting, or the like. By applying an acrylic adhesive to such a film and drying it, a polyvinyl chloride resin adhesive film according to the present invention can be obtained. As the acrylic adhesive, a common adhesive conventionally used for polyvinyl chloride resin adhesive films can be used.

光馴V杉丸果 以上のように、本発明によれば、アクリル系粘着剤層を
有する半硬質ポリ塩化ビニル系樹脂粘着フィルムにおい
て、基材を構成する塩化ビニル系樹脂に液状可塑剤と共
に所定量のハイドロタルザイ)M化合物を配合すること
によって、上記可塑剤の粘着剤層の移行を防止し、粘着
力の経時紙トをよく抑えることができ、しかも、かくし
て得られるフィルムは、印刷性、耐熱性、耐候性等にも
すぐれるので、マーキングフィルム、マスキングテープ
、保護フィルム等に好適に用いることができる。
As described above, according to the present invention, in a semi-rigid polyvinyl chloride resin adhesive film having an acrylic adhesive layer, a predetermined amount of a liquid plasticizer is added to the vinyl chloride resin constituting the base material. By blending the hydrotarzai) M compound, it is possible to prevent the transfer of the above-mentioned plasticizer to the adhesive layer and to suppress the deterioration of adhesive strength over time, and the film thus obtained has excellent printability, Since it has excellent heat resistance, weather resistance, etc., it can be suitably used for marking films, masking tapes, protective films, etc.

ス」1舛 以下に実施例を挙げて本発明を説明するが、本発明はこ
れら実施例により何ら限定されるものではない。
The present invention will be described below with reference to Examples, but the present invention is not limited to these Examples in any way.

第1表に示す配合にて塩化ビニル樹脂組成物を調製し、
175℃、12インチ、2本ロールにて5分間混練し、
これを厚さ0.11−のフィルムに加工した。これらフ
ィル1、について、以下の試験を行なった。
A vinyl chloride resin composition was prepared with the formulation shown in Table 1,
Knead for 5 minutes at 175°C, 12 inches, with two rolls,
This was processed into a 0.11-thick film. The following tests were conducted on these films 1.

粘着力保持性 フィルムにアクリル系粘着剤(東洋インキ■製BPS−
5213/BH3−8515(10/2)の混合物)を
厚さ30μmに塗布し、乾燥硬化させ、この粘着剤層の
上に離型紙を貼着した。
Acrylic adhesive (BPS- manufactured by Toyo Ink ■) on adhesive strength film
5213/BH3-8515 (10/2 mixture)) was applied to a thickness of 30 μm, dried and cured, and a release paper was pasted on the adhesive layer.

この粘着フィルムを約80℃のオーブン中にて7日間放
置した後、2511幅の短冊状に裁断し、離型紙を剥離
し、ステンレス鋼(SUS304)板上にゴムロールを
用いて貼り付けた。次いで、ショツパー試験装置を用い
て、室温にて200鶴/分の速度にてフィルムの剥離接
着力を測定した。
This adhesive film was left in an oven at about 80° C. for 7 days, then cut into strips with a width of 2511 mm, the release paper was peeled off, and the strips were pasted onto a stainless steel (SUS304) plate using a rubber roll. The peel adhesion of the film was then measured using a Schopper tester at room temperature and at a rate of 200 per minute.

この加熱処理後のフィルムの剥離接着力と加熱処理前の
それとから、次式に基づいて、粘着力保持性(%)を求
めた。
Based on the peel adhesive strength of the film after the heat treatment and that before the heat treatment, the adhesive force retention (%) was determined based on the following formula.

印刷性 フィルムを温度約70℃、湿度約90%の恒温恒湿槽に
14日間放置した後、フィルムに印刷インキ(大日本イ
ンキ化学工業■性105Y紅)を厚さ約20μmに塗布
し、1日間放置した。この後、印刷インキ上にセロハン
テープを圧着し、次いで、速やかにセロハンテープを剥
がして、インキの剥離状況を目視にて観察した。Oはイ
ンキの剥離がなかったことを示す。
After the printable film was left in a constant temperature and humidity chamber at a temperature of about 70°C and a humidity of about 90% for 14 days, printing ink (Dainippon Ink Chemical Industry 105Y Red) was applied to the film to a thickness of about 20 μm. I left it for days. Thereafter, a cellophane tape was pressed onto the printing ink, and then the cellophane tape was immediately peeled off, and the state of ink peeling was visually observed. O indicates that there was no ink peeling.

耐候性 フィルムをアルミニウム板に貼り付け、サンシャイン・
ウエザオ・メーター(スガ試験機■製WE−5UN−I
C型サンシャイン・ウェザ−・メーター)63℃、降雨
12分/60分で1000時間照射して、かかる照射を
しなかった試料との色差を色差計(日本重色工業■製S
Z−Σ80型)にて測定した。
A weather-resistant film is pasted on an aluminum plate, and sunshine
Weathero meter (WE-5UN-I made by Suga Test Instruments)
C-type Sunshine Weather Meter) 63℃, 12 minutes of rain/60 minutes of irradiation for 1,000 hours, and the color difference between the sample and the sample that was not irradiated was measured using a color difference meter (S
Z-Σ80 type).

(第1表の注) 1)チッソ■製ニポリットSL。(Note to Table 1) 1) Nipolit SL manufactured by Chisso ■.

2)大日本インキ化学工業〔菊製W −305ELS、
3)大日本インキ化学工業■製W −1200El、S
、4)大日本インキ化学工業側製W −100ELS、
5)共同薬品Il製、 6)昭島化学工業■製、 7)日本チバガイギーー製チヌビン326.8)協和化
学工業■製アルカマイザー■(Mgo、67八lo、3
3(OH)2(GO3)0.+as・0.50HzO)
9)協和化学工業■製、DHT−4’A(Mgt、 、
612(Olり +3CO3・3.5H20)温にて2
00m/分の引張速度にて測定した。
2) Dainippon Ink and Chemicals [Kiku W-305ELS,
3) W-1200El, S manufactured by Dainippon Ink and Chemicals
, 4) W-100ELS manufactured by Dainippon Ink and Chemicals,
5) Kyodo Yakuhin Il, 6) Akishima Chemical Industry ■, 7) Japan Ciba Geigy Tinuvin 326.8) Kyowa Chemical Industry ■ Alkamizer ■ (Mgo, 678 lo, 3
3(OH)2(GO3)0. +as・0.50HzO)
9) DHT-4'A (Mgt, , manufactured by Kyowa Chemical Industry ■)
2 at 612 (Ol +3CO3・3.5H20) temperature
The measurement was carried out at a tensile speed of 00 m/min.

以上の結果を第1表に示す。The above results are shown in Table 1.

耐熱性 フィルムを約160°Cのギヤーオーブン中に40分間
放置し、かかる熱処理を行なわなかった試料との色差を
色差計(日本重色工業■製SZ−Σ80型)にて測定し
た。
The heat-resistant film was left in a gear oven at about 160° C. for 40 minutes, and the color difference between it and a sample that had not been subjected to such heat treatment was measured using a color difference meter (Model SZ-Σ80 manufactured by Nippon Heavy Industries Ltd.).

張力強度及び伸びTensile strength and elongation

Claims (1)

【特許請求の範囲】[Claims] (1)塩化ビニル系重合体100重量部について、液状
可塑剤を10〜45重量部とハイドロタルサイト類化合
物を0.1〜5重量部含有する塩化ビニル系樹脂からな
るフィルムにアクリル系粘着剤層を設けてなる半硬質ポ
リ塩化ビニル系樹脂粘着フィルム。
(1) An acrylic pressure-sensitive adhesive is applied to a film made of a vinyl chloride resin containing 10 to 45 parts by weight of a liquid plasticizer and 0.1 to 5 parts by weight of a hydrotalcite compound based on 100 parts by weight of a vinyl chloride polymer. A semi-rigid polyvinyl chloride resin adhesive film with layers.
JP29703488A 1988-11-24 1988-11-24 Polyvinyl chloride resin adhesive film Expired - Fee Related JP2587280B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29703488A JP2587280B2 (en) 1988-11-24 1988-11-24 Polyvinyl chloride resin adhesive film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29703488A JP2587280B2 (en) 1988-11-24 1988-11-24 Polyvinyl chloride resin adhesive film

Publications (2)

Publication Number Publication Date
JPH02142877A true JPH02142877A (en) 1990-05-31
JP2587280B2 JP2587280B2 (en) 1997-03-05

Family

ID=17841364

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29703488A Expired - Fee Related JP2587280B2 (en) 1988-11-24 1988-11-24 Polyvinyl chloride resin adhesive film

Country Status (1)

Country Link
JP (1) JP2587280B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103524927A (en) * 2013-09-29 2014-01-22 苏州华周胶带有限公司 High-strength polyvinyl chloride tape substrate
JPWO2015141171A1 (en) * 2014-03-18 2017-04-06 日本ゼオン株式会社 Vinyl chloride resin composition, vinyl chloride resin molded body and laminate

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103524927A (en) * 2013-09-29 2014-01-22 苏州华周胶带有限公司 High-strength polyvinyl chloride tape substrate
JPWO2015141171A1 (en) * 2014-03-18 2017-04-06 日本ゼオン株式会社 Vinyl chloride resin composition, vinyl chloride resin molded body and laminate

Also Published As

Publication number Publication date
JP2587280B2 (en) 1997-03-05

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