JPS6088049A - Biaxially oriented polypropylene film - Google Patents

Biaxially oriented polypropylene film

Info

Publication number
JPS6088049A
JPS6088049A JP19680183A JP19680183A JPS6088049A JP S6088049 A JPS6088049 A JP S6088049A JP 19680183 A JP19680183 A JP 19680183A JP 19680183 A JP19680183 A JP 19680183A JP S6088049 A JPS6088049 A JP S6088049A
Authority
JP
Japan
Prior art keywords
film
biaxially oriented
oriented polypropylene
polypropylene film
crystalline
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
JP19680183A
Other languages
Japanese (ja)
Other versions
JPS646655B2 (en
Inventor
Seiji Murakami
村上 征次
Mamoru Furuko
守 古胡
Kiroku Taniguchi
谷口 紀六
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP19680183A priority Critical patent/JPS6088049A/en
Publication of JPS6088049A publication Critical patent/JPS6088049A/en
Publication of JPS646655B2 publication Critical patent/JPS646655B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:The titled film having excellent transparency, slipperiness, and blocking resistance, obtained by molding a resin composition, consisting of a specified crystalline PP, nucleator, and Si compound, in the form of a film. CONSTITUTION:0.01-1.0pts.wt. nucleator (e.g. sodium adipate), and 0.05-2.0pts. wt. inorganic or organic Si compound having an average diameter of 0.2-5.0mu (e.g. synthetic zeolite) are incorporated into 100pts.wt. crystalline PP, having an intrinsic viscosity [eta] of tetralin solution at 135 deg.C of 1.0-2.0, an isotactic index of at least 98%, to obtain the resin composition. Then, the composition is molded in the form of a film, which is stretched biaxially, 3-7 times longitudinally and 5-15 times transversely, producing a biaxially oriented PP film having a gloss value of at least 145 and a thickness of 5-150mu.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は二軸延伸ポリプロピレンフィルムに関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to biaxially oriented polypropylene films.

〔従来の技術〕[Conventional technology]

従来の二軸延伸ポリプロピレンフィルムとしては通常の
ポリプロピレンに造核剤を添カII して透明性を改良
したものが知られている。しかしこのフィルムは光沢度
の大巾改良がなく、滑シ性、耐ブロッキング性に劣って
いたので有機滑剤(例えば脂肪酸アミド)、無機滑剤を
添加しなければならが生じていた。
As a conventional biaxially oriented polypropylene film, one in which a nucleating agent is added to ordinary polypropylene to improve transparency is known. However, this film did not significantly improve gloss and was poor in lubricity and anti-blocking properties, necessitating the addition of an organic lubricant (eg fatty acid amide) or an inorganic lubricant.

〔発明の目的〕[Purpose of the invention]

本発明の目的は上記欠点を解消せしめ、光沢度145以
上で透明性に優れ、滑べりやすく、プロツキ/グしにく
い二軸延伸ポリプロピレンフィルムを提供せんとするも
のである。
The object of the present invention is to eliminate the above-mentioned drawbacks and to provide a biaxially oriented polypropylene film which has a gloss level of 145 or more, has excellent transparency, is easy to slip, and is difficult to scratch/print.

〔発明の構成〕[Structure of the invention]

本発明は上記目的を達成するため次の構成、すなわち、
極限粘度[v)1.0〜20.アインタクチック度98
%以上の結晶性ポリプロピレン100重量部に対し、造
核剤0.01〜1,0重量部、ケイ素化合物0・05〜
2O7JL歇部を含有し、光沢度が145以上の二軸延
伸ポリプロビレ/フィルム’t4I徴とするものである
In order to achieve the above object, the present invention has the following configuration, namely:
Intrinsic viscosity [v) 1.0-20. Intactic degree 98
% or more of crystalline polypropylene, 0.01 to 1.0 parts by weight of a nucleating agent, and 0.05 to 1.0 parts by weight of a silicon compound.
It is a biaxially oriented polypropylene/film 't4I containing 2O7JL edge part and having a gloss level of 145 or more.

本発明における結晶性ポリプロピレンとは、165°C
テトラリン溶液での極限粘度〔η〕が10〜2、0の範
囲にあシ、好ましくは1.1〜1.95の範囲であり沸
騰n−へブタンで12時間抽出後の残渣の100分率(
アイソタクチツク度)98チ以上のプロピレン重合体を
いう。二軸延伸ポリプロピレンの極限粘度〔η〕が本発
明の範囲に入る結晶性ポリプロピレンのベレット〔η〕
は11〜2.1にあることが、熱誠性による低下からみ
て必要であるが、好ましい結晶性ポリプロピレンベレッ
トの〔η〕 は12〜20の範囲にあるものである。
In the present invention, crystalline polypropylene means 165°C
The intrinsic viscosity [η] in a tetralin solution is in the range of 10 to 2.0, preferably in the range of 1.1 to 1.95, and is 100% of the residue after extraction with boiling n-hebutane for 12 hours. (
A propylene polymer with an isotactic degree of 98 degrees or higher. Crystalline polypropylene pellet [η] whose intrinsic viscosity [η] of biaxially oriented polypropylene falls within the range of the present invention
It is necessary that [η] be in the range of 11 to 2.1 in view of the decrease in thermal integrity, but it is preferable that [η] of the crystalline polypropylene pellet be in the range of 12 to 20.

但しアイソタクチツク度は本発明の範囲を同時に満足す
ることが必須要件である。
However, it is essential that the degree of isotacticity satisfies the scope of the present invention.

ベレット段階での〔η〕 がここにいう範囲にするには
1重合段階でこの範囲になるよう規制し。
In order for [η] at the pellet stage to be within the range mentioned here, it must be regulated to be within this range for one polymerization stage.

結晶性ポリプロピレンを得ることができるが、高い〔η
〕 の結晶性ポリプロピレンを熱誠性、あるいは有機過
酸化物(例えば2−6ジターシヤリブチルパーオキシヘ
キサン)を添加しての熱誠性によって、ここにいう〔η
〕 の範囲の結晶性ポリプロピレンを得ることができる
。延伸においては後者が好ましいことがある。
Although crystalline polypropylene can be obtained, the high [η
] The crystalline polypropylene of [η
] It is possible to obtain crystalline polypropylene in the range of . The latter may be preferred in stretching.

本発明において、極限粘度〔η〕 が上記の範囲を外れ
るものは延伸し難いものであったり、光沢クチツク度が
98nl)を下まわるものは、光沢度。
In the present invention, those whose intrinsic viscosity [η] is outside the above range are difficult to stretch, and those whose glossiness is less than 98 nl) are considered glossy.

透明性が低い、劣ったものとなり、高光沢の透明性のす
ぐれたものになりにくい。
The transparency becomes low and inferior, and it is difficult to achieve high gloss and excellent transparency.

造核剤とは結晶の核となって、結晶を成長させるのに効
果のある物質をいい、具体的には、アジヒン酸ナトリウ
ム、安息香酸ナトリウム、アジピン酸アルミニウム、タ
ーシャリ安息香酸アルミニウム、安息香酸アルミニウム
や、ジベンジリテンンルビトール及びその誘導体が望葦
しい。
A nucleating agent is a substance that acts as a nucleus for a crystal and is effective in growing the crystal.Specifically, it includes sodium adiphate, sodium benzoate, aluminum adipate, aluminum tertiary benzoate, and aluminum benzoate. , dibenzyritene rubitol and its derivatives are desirable.

造核剤の添加量は、前記結晶性ポリプロピレン100重
量部に対し、001〜1.0重量部、好ましくは002
〜05N量部であシ、この範囲に414たないと造核剤
の効果が小さく、またこの範囲を越えると、フィルム表
面からにじみ出し、フィルムの製造過程でロール等へ何
着転移し、フィルム表面を汚し、透明性、光沢度を落と
すことになる。
The amount of the nucleating agent added is 0.001 to 1.0 parts by weight, preferably 0.02 to 1.0 parts by weight, based on 100 parts by weight of the crystalline polypropylene.
If the amount is less than 414 N, the effect of the nucleating agent will be small, and if it exceeds this range, it will ooze out from the film surface, transfer to rolls etc. during the film manufacturing process, and cause the film to deteriorate. It stains the surface and reduces transparency and gloss.

ケイ素化合物とは、無機、有機のケイ素化合物をいう。The silicon compound refers to inorganic and organic silicon compounds.

無機のケイ素化合物としては、二酸化ケイ素、ケイ酸ア
ルミニウム、ケイ酸アルミニウムソーダなどがあシ、具
体的にはサイロイド、シリカ、雲母、クルク、ケイソウ
土、カオリン、カオリナイト、ベントナイト、天然ゼオ
ライト、合成ゼオライトなどがあげられ滑剤の役割を果
たすものである。好ましい平均粒子径は0.2〜5,0
μである。
Inorganic silicon compounds include silicon dioxide, aluminum silicate, aluminum silicate soda, etc., specifically thyroid, silica, mica, curcum, diatomaceous earth, kaolin, kaolinite, bentonite, natural zeolite, synthetic zeolite. These substances play the role of lubricants. The preferred average particle size is 0.2 to 5.0
μ.

有機のケイ素化合物としては、シリコーンオイルが上け
られる。粘度は40〜4[1,O[l[lセンチストー
クス(25℃)のもので具体的には、メチルエチルポリ
シロキサン、メチルハイドロジエボリシロキサン、ジメ
テルポリシロキザン、ジメチルボリシロキザンの一部メ
チル基に他の有機基を導入した変性シリコーンオイル、
それらの例としてアミ7基、カルボキシル基、ポリオギ
シアルキレン基、長鎖アルキル基、エポキシ基などがあ
る。
Silicone oil is cited as an organic silicon compound. The viscosity is 40 to 4[1,0[l[l] centistokes (25°C), and specifically, it is one of methylethylpolysiloxane, methylhydrodievorisiloxane, dimethylpolysiloxane, and dimethylborisiloxane. Modified silicone oil with other organic groups introduced into the methyl group,
Examples of these include amide 7 groups, carboxyl groups, polyoxyalkylene groups, long-chain alkyl groups, and epoxy groups.

この中でもジメチルポリシロキサン、ポリオキシアルキ
レン変性ポリシロキサン、長鎖アルキル変性ポリシロキ
サンなどの−又は混合物が好壕しく。
Among these, dimethylpolysiloxane, polyoxyalkylene-modified polysiloxane, long-chain alkyl-modified polysiloxane, etc. or a mixture thereof are preferred.

滑ベシ性、耐ブロッキング性、さらに[防止性を付与で
きることもある。
Smoothness, anti-blocking properties, and even anti-blocking properties can be imparted in some cases.

添加量としては、前記結晶性ポリプロ2ン7100重量
部に対し0.05〜20重量部、さらに好ましい添力1
1量は0.07〜10重量部の範囲である。005重社
部を下まわる場合は滑ベシ性、耐ブロッキング性に劣シ
、20重量部を越えると。
The amount added is 0.05 to 20 parts by weight, more preferably 1 to 7100 parts by weight of the crystalline polypropylene.
One amount ranges from 0.07 to 10 parts by weight. If the amount is less than 005, the slipping properties and blocking resistance will be poor, and if it exceeds 20 parts by weight.

光沢度が低下し、透明性に劣るものとなる。The gloss level decreases and the transparency becomes inferior.

無機、有機のケイ素化合物を併用添力1] しても良い
が添加量は本発明の範囲内であることは云う壕でもない
Although inorganic and organic silicon compounds may be added in combination, the amount added is within the scope of the present invention.

なお、ケイ素化合物の識別は9発光分光あるいは吸光分
光分析によシケイ素を含有することを判定し1本フィル
ムの灰分(空気中で850 ’Oにて加熱灰化しての灰
分の百分率を測定し、0.045〜1.8 w t%の
範囲に灰分がある場合は、ケイ素化合物が本発明の11
1四内にあると判定する。
In addition, to identify silicon compounds, it is determined that they contain silicon by 9 emission spectroscopy or absorption spectroscopy, and the ash content of one film (by heating and ashing at 850'O in air and measuring the percentage of ash content) is determined. , when the ash content is in the range of 0.045 to 1.8 wt%, the silicon compound is
It is determined that it is within 14.

また光沢度(as−60)が145以上あるのでグリン
トラミネート用フィルム、離型用フィルム、粘着チーブ
用フィルム、包装材等として、高級で、かつ特殊用途と
することができる。
In addition, since it has a gloss level (AS-60) of 145 or more, it can be used for high-grade and special purposes such as glitter laminating films, release films, adhesive films, packaging materials, etc.

本発明の二軸延伸ポリプロピレンフィルムは。The biaxially oriented polypropylene film of the present invention is.

逐次延伸、同時延伸のいずれであっても良い。延伸倍率
は長手方向6〜7倍、横手方向5〜15倍の範囲が好ま
しい。
Either sequential stretching or simultaneous stretching may be used. The stretching ratio is preferably 6 to 7 times in the longitudinal direction and 5 to 15 times in the transverse direction.

フィルム厚みは特に限定しないが、5〜150μが好筐
しく用いられる。
Although the film thickness is not particularly limited, 5 to 150 μm is preferably used.

なお結晶性ポリプロピレンには、安定剤、酸化防止剤、
紫外線吸収剤、耐候剤、帯電防止剤9着色剤、増白剤等
を添加しても良い。
Crystalline polypropylene contains stabilizers, antioxidants,
Ultraviolet absorbers, weathering agents, antistatic agents, colorants, brighteners, etc. may be added.

本発明の特性値は次の測定法によるものである。The characteristic values of the present invention are determined by the following measurement method.

(1)極限粘度〔η〕 1ろ5 ’Oテトラリン溶液での相対粘度を測定し。(1) Intrinsic viscosity [η] Measure the relative viscosity in a 1-5'O tetralin solution.

極限粘度〔η〕 をめる。Calculate the intrinsic viscosity [η].

(2) アイソタクチック度(工、工)沸騰n−へブタ
ンで12時間抽出後の残渣重量を抽出前の重量で計算し
た百分率をいう。但し。
(2) Isotactic degree (technical, technical) refers to the percentage of the weight of the residue after extraction with boiling n-hebutane for 12 hours based on the weight before extraction. however.

抽出前の重量とは、造核剤等の添加剤を抜いた値をいう
The weight before extraction refers to the value excluding additives such as nucleating agents.

(3) 光沢度 J工S−28741の方法2による値をいい、この値が
高い程、光沢度に優れていることをいう。
(3) Glossiness This refers to the value according to Method 2 of J Engineering S-28741, and the higher the value, the better the glossiness.

(4) ヘイズ(透明性の評価) J工S−に6714によ9.8枚ヘイズとは8枚重ねて
測定した値をいう。ヘイズ値が低いと透明性が優れてい
ることを意味する。
(4) Haze (Evaluation of Transparency) 9.8 sheets were measured using 6714 on J-Ko S-Haze means the value measured by stacking 8 sheets. A low haze value means excellent transparency.

(5)滑ベシ係数 20℃、65%RHの室内で24時間調湿した2枚の試
料の相反する面とおしを重ねて、その上に200gの荷
重金乗せて、一枚の試料を150二/分の速度で移動さ
せてその抵抗値を読み、抵抗値(g)/2DDgの計算
値で示した。
(5) Sliding coefficient: Two samples were conditioned for 24 hours in a room with a humidity of 20°C and 65% RH.The opposite sides of the two samples were stacked on top of each other, and a 200g load was placed on top of the two samples. The resistance value was read while moving at a speed of 1/min, and was expressed as a calculated value of resistance value (g)/2DDg.

(6) ブロッキング剪断力(面1ブロッキング性の評
価〕 幅3cmx長さ10cn1の試料フィルムを長さ4 c
mにわたって重ね合せて、40°0,80%RHの雰囲
気中に40 g 7cm°の荷重で24時間放置した後
(6) Blocking shear force (evaluation of surface 1 blocking property) A sample film of width 3 cm x length 10 cn1 was
After being stacked for 24 hours under a load of 40 g 7 cm ° in an atmosphere of 40 ° 0, 80% RH.

引張り試験機で剪断剥離に要する力を迎1定する。The force required for shear peeling is determined using a tensile tester.

数値が小さいほど剛ブロッキング性は良い。The smaller the value, the better the rigid blocking property.

〔発明の効果〕〔Effect of the invention〕

本発明は上述したように、特定の結晶性ポリプロピレン
に造核剤、ケイ素化合物を特定量添加した二軸延伸ポリ
プロピレンフィルムとしたので。
As described above, the present invention is a biaxially oriented polypropylene film in which a specific amount of a nucleating agent and a silicon compound are added to specific crystalline polypropylene.

光沢度145以上で透明性に優れ、滑ベシ性、耐ブロッ
キングを満足するフィルムとすることができたのである
We were able to create a film with a gloss level of 145 or higher, excellent transparency, and satisfactory lubricity and anti-blocking properties.

本発明の二軸延伸ポリプロピレンフィルムは。The biaxially oriented polypropylene film of the present invention is.

プリントラミネート(印刷物への貼合せ)用途。For print lamination (attaching to printed materials).

#型用途、包装材、粘着テープ等の高級、特殊用途に適
したフィルムである。
This film is suitable for high-grade and special uses such as #-type applications, packaging materials, and adhesive tapes.

〔実施例〕〔Example〕

次に実施例に基づいて本発明の実施態様を説明する。 Next, embodiments of the present invention will be described based on Examples.

表−1に示す組成と特性を有する結晶性ポリプロピレン
を押出機に供給し、280℃でTダイよシ押出し冷却ド
ラムに巻付け750μのシートとした。該シートtロー
ル群で120°Cに加熱しつつ長手方向に5倍に延伸、
冷却し、175’Oに加熱したテンター内に導き約10
倍に横手方向に延伸、さらに5%の弛緩率を155°C
の雰囲気であたえ15μの二軸延伸ポリプロピレンフィ
ルムとし1片面にコロナ放電処理を施した。結果につい
ては表−1に1とめて示した。
Crystalline polypropylene having the composition and properties shown in Table 1 was fed to an extruder, extruded through a T-die at 280°C, and wound around a cooling drum to form a 750μ sheet. Stretch the sheet 5 times in the longitudinal direction while heating it to 120°C with a group of T-rolls,
It was cooled and introduced into a tenter heated to 175'O for about 10 minutes.
Stretched twice in the transverse direction and further relaxed at 5% at 155°C.
A biaxially stretched polypropylene film having a thickness of 15 μm was prepared in an atmosphere of 1, and one side of the film was subjected to a corona discharge treatment. The results are listed in Table 1.

本発明の実施例1,2は光沢度が大巾に向上し。In Examples 1 and 2 of the present invention, the glossiness was greatly improved.

ヘイズの低い透明性に優れた。さらには滑べり性。Excellent transparency with low haze. Furthermore, it is slippery.

耐ブロッキング性にも優れたフィルムとなった。The film also has excellent anti-blocking properties.

実施例2においては、帯電防止性をも持ち合せたフィル
ムとなった。
In Example 2, the film also had antistatic properties.

反面、比較例では、ヘイズや光沢度に劣る比較例1.す
ベシ性やブロッキングに劣る比較例2゜添加量が多いた
めにロールに付着し、それがフィルム表面に付着し、ヘ
イズ、光沢度、さらに滑ベシ係数、ブロッキング剪断力
が悪化した比較例6゜多数のボイドとなってヘイズ、光
沢度を悪くさせた比較例4.高〔η〕低エエの比較例5
は光沢度。
On the other hand, Comparative Example 1. is inferior in haze and glossiness. Comparative Example 2, which is inferior in surface properties and blocking; Comparative Example 6, in which the addition amount is large, so it adheres to the roll, and it adheres to the film surface, resulting in poor haze, glossiness, sliding coefficient, and blocking shear force. Comparative Example 4, where a large number of voids were formed, resulting in poor haze and gloss. High [η] low air comparative example 5
is the glossiness.

ヘイズに劣り + j% Cη〕。低エエで無添加の比
較例6は全ての面に劣った。
Inferior to haze + j% Cη]. Comparative Example 6 with low air content and no additives was inferior in all aspects.

なお本発明のフィルムをプリントラミネート用途(印刷
物に貼合せ)に加工したところ9鮮明でかつ光沢ある印
刷物となった。
When the film of the present invention was processed for print lamination (laminated onto printed matter), the resulting printed matter was clear and glossy.

手 続 補 正 轡 1.事flの表示 昭和58年特許願第196801J’32、発明の名称 二輪延伸ポリプロピレンフィルム 3、補正をする者 自発 5、補正により増加する発明の数 なし 6、補正の対象 明細書の「発明の詳細な説明」の欄 7、補正の内容 (1) 明IIIfq 第6頁13行L1「百分率を測
定」を1百分率)をat++定」と補正する。
Procedure amendment 轡1. Indication of the matter fl 1982 Patent Application No. 196801J'32, Name of the invention: Two-wheel stretched polypropylene film 3, Amendr's initiative 5, No number of inventions increased by the amendment 6, ``Details of the invention'' in the specification subject to the amendment Column 7, "Explanation", Contents of Correction (1) Mei IIIfq Page 6, Line 13, L1 "Measure percentage" is corrected to "at++ constant" (1%).

(2) 同 第11頁 表−1゛比較6パの行、パペレ
ツ1〜″の1.1”の欄 [9,75Jを+ 97.5Jと補正づる。
(2) Same page 11 Table 1 Comparison 6th row, 1.1" column of paperset 1~" [9,75J is corrected to +97.5J.

Claims (1)

【特許請求の範囲】[Claims] (1) 極限粘度〔η〕1.0〜2.o、アイソタクチ
ック度98%以上の結晶性ポリプロピレン1ooz量部
に対し、造核剤o、 o i 〜i、 ozzff+s
、 クイ素化合物0.05〜20重量部を含有し、光沢
度が145以上の二軸延伸ポリプロピレンフィルム。
(1) Intrinsic viscosity [η] 1.0-2. o, 1 oz part of crystalline polypropylene with an isotactic degree of 98% or more, nucleating agent o, o i ~i, ozzzff+s
, A biaxially oriented polypropylene film containing 0.05 to 20 parts by weight of a quinine compound and having a glossiness of 145 or more.
JP19680183A 1983-10-20 1983-10-20 Biaxially oriented polypropylene film Granted JPS6088049A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19680183A JPS6088049A (en) 1983-10-20 1983-10-20 Biaxially oriented polypropylene film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19680183A JPS6088049A (en) 1983-10-20 1983-10-20 Biaxially oriented polypropylene film

Publications (2)

Publication Number Publication Date
JPS6088049A true JPS6088049A (en) 1985-05-17
JPS646655B2 JPS646655B2 (en) 1989-02-06

Family

ID=16363871

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19680183A Granted JPS6088049A (en) 1983-10-20 1983-10-20 Biaxially oriented polypropylene film

Country Status (1)

Country Link
JP (1) JPS6088049A (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60118727A (en) * 1983-12-01 1985-06-26 Toyo Soda Mfg Co Ltd Soft polypropylene composition for film
JPS62115049A (en) * 1985-11-14 1987-05-26 Sumitomo Chem Co Ltd Impact-resistant polypropylene composition
JPH01141029A (en) * 1987-11-27 1989-06-02 Toray Ind Inc Print laminate and its manufacture
JPH01214422A (en) * 1988-02-23 1989-08-28 Toray Ind Inc Manufacture of thermoplastic resin film
JPH024808A (en) * 1988-06-23 1990-01-09 Toray Ind Inc Polypropylene film for tacky tape
EP0399492A2 (en) * 1989-05-23 1990-11-28 MITSUI TOATSU CHEMICALS, Inc. Stretched films of polypropylene
EP0629632A3 (en) * 1993-06-07 1995-03-08 Mitsui Petrochemical Ind Novel transition metal compound for use as a polymerization catalyst.
EP0732993A4 (en) * 1993-12-09 1997-03-12 Mobil Oil Corp Release film for label stock
SG89428A1 (en) * 2000-11-24 2002-06-18 Sumitomo Chemical Co Polypropylene resin composition and injection molded article
JP2002536520A (en) * 1999-02-10 2002-10-29 トレスパファン、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング Transparent biaxially oriented polyolefin film
US7378467B2 (en) 2003-09-22 2008-05-27 Er Ming Yan Zeolite anti-blocking agents
JP2009520093A (en) * 2005-12-20 2009-05-21 バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ Polypropylene composition for articles to be stretched
WO2009084391A1 (en) * 2007-12-27 2009-07-09 Kureha Corporation Polypropylene resin composition, molded article produced from the resin composition, and method for production of the molded article
JP2015201616A (en) * 2014-03-31 2015-11-12 王子ホールディングス株式会社 Biaxially stretched polypropylene film for capacitor
EP3196235A4 (en) * 2014-09-19 2018-05-09 Toray Industries, Inc. Polypropylene film and film capacitor

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS506650A (en) * 1973-05-22 1975-01-23
JPS51135976A (en) * 1975-05-20 1976-11-25 Matsushita Electric Ind Co Ltd Transmissive films
JPS564642A (en) * 1979-06-26 1981-01-19 Mitsubishi Petrochem Co Ltd Propylene polymer film

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS506650A (en) * 1973-05-22 1975-01-23
JPS51135976A (en) * 1975-05-20 1976-11-25 Matsushita Electric Ind Co Ltd Transmissive films
JPS564642A (en) * 1979-06-26 1981-01-19 Mitsubishi Petrochem Co Ltd Propylene polymer film

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60118727A (en) * 1983-12-01 1985-06-26 Toyo Soda Mfg Co Ltd Soft polypropylene composition for film
JPH0472854B2 (en) * 1983-12-01 1992-11-19 Tosoh Corp
JPS62115049A (en) * 1985-11-14 1987-05-26 Sumitomo Chem Co Ltd Impact-resistant polypropylene composition
JPH01141029A (en) * 1987-11-27 1989-06-02 Toray Ind Inc Print laminate and its manufacture
JPH0528976B2 (en) * 1987-11-27 1993-04-28 Toray Industries
JPH01214422A (en) * 1988-02-23 1989-08-28 Toray Ind Inc Manufacture of thermoplastic resin film
JPH024808A (en) * 1988-06-23 1990-01-09 Toray Ind Inc Polypropylene film for tacky tape
EP0399492A2 (en) * 1989-05-23 1990-11-28 MITSUI TOATSU CHEMICALS, Inc. Stretched films of polypropylene
EP0629632A3 (en) * 1993-06-07 1995-03-08 Mitsui Petrochemical Ind Novel transition metal compound for use as a polymerization catalyst.
EP0732993A4 (en) * 1993-12-09 1997-03-12 Mobil Oil Corp Release film for label stock
SG84481A1 (en) * 1993-12-09 2001-11-20 Mobil Oil Corp Release film for label stock
JP2002536520A (en) * 1999-02-10 2002-10-29 トレスパファン、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング Transparent biaxially oriented polyolefin film
SG89428A1 (en) * 2000-11-24 2002-06-18 Sumitomo Chemical Co Polypropylene resin composition and injection molded article
US7378467B2 (en) 2003-09-22 2008-05-27 Er Ming Yan Zeolite anti-blocking agents
JP2009520093A (en) * 2005-12-20 2009-05-21 バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ Polypropylene composition for articles to be stretched
WO2009084391A1 (en) * 2007-12-27 2009-07-09 Kureha Corporation Polypropylene resin composition, molded article produced from the resin composition, and method for production of the molded article
JPWO2009084391A1 (en) * 2007-12-27 2011-05-19 株式会社クレハ Polypropylene resin composition, molded article comprising the resin composition, and method for producing the molded article
JP2015201616A (en) * 2014-03-31 2015-11-12 王子ホールディングス株式会社 Biaxially stretched polypropylene film for capacitor
EP3196235A4 (en) * 2014-09-19 2018-05-09 Toray Industries, Inc. Polypropylene film and film capacitor

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