JPS61281142A - Resin composition for extrusion molding - Google Patents

Resin composition for extrusion molding

Info

Publication number
JPS61281142A
JPS61281142A JP61099796A JP9979686A JPS61281142A JP S61281142 A JPS61281142 A JP S61281142A JP 61099796 A JP61099796 A JP 61099796A JP 9979686 A JP9979686 A JP 9979686A JP S61281142 A JPS61281142 A JP S61281142A
Authority
JP
Japan
Prior art keywords
component
weight
film
zeolite
resin composition
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
JP61099796A
Other languages
Japanese (ja)
Other versions
JPS648018B2 (en
Inventor
Koji Yamamoto
孝二 山本
Akinori Onishi
大西 明憲
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.)
Mitsubishi Petrochemical Co Ltd
Original Assignee
Mitsubishi Petrochemical Co 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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP61099796A priority Critical patent/JPS61281142A/en
Publication of JPS61281142A publication Critical patent/JPS61281142A/en
Publication of JPS648018B2 publication Critical patent/JPS648018B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a resin composition obtained by compounding a specific ethylene copolymer with zeolite and an organic amide compound, and having excellent transparency, well-balanced slipperiness and printability and practically acceptable blocking property. CONSTITUTION:The objective composition is produced by compounding (A) 100pts.(wt.) of an ethylene copolymer produced by the use of a Ziegler catalyst and having a density of 0.910-0.940g/cm<3>, a melt flow rate of 0.01-20g/10min and a comonomer content of 1-10wt% with (B) 0.01-1pt. of zeolite having an average particle diameter of <=20mu and (C) 0.01-1pt. of an organic amide compound obtained by mixing a saturated fatty acid amide to an unsaturated fatty acid amide at a ratio of about 3:1.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、実用性に供しえるブロッキング性を有しなが
ら透明性、スリップ性及び印刷性のバランスの良好な線
型のエチレン共重合体の押出成形用樹脂組成物に関する
Detailed Description of the Invention [Industrial Application Field] The present invention is directed to the extrusion of a linear ethylene copolymer that has blocking properties suitable for practical use and has a good balance of transparency, slip properties, and printability. The present invention relates to a molding resin composition.

〔従来の技術〕[Conventional technology]

透明性の良好なフィルムなどの押出し成形品材料として
、従来からポリプロピレンが知られている。このポリプ
ロピレンフィルムは、剛性等も優れることから各種包装
材として広く用いられている。
Polypropylene has been known as a material for extruded products such as films with good transparency. This polypropylene film is widely used as various packaging materials because of its excellent rigidity.

ところが、ポリプロピレンフィルムは、一方で空冷イン
フレーション成形といった汎用的加工法に適していない
ことや、衝撃強度(特に低温衝撃強度)や低温ヒートシ
ール性が劣る欠点を有しているので、その用途分野は限
定されてきた。従って、汎用的フィルム分野では、これ
らの欠点を補う・樹脂である高圧法低密度ポリエチレン
及び低圧法高密度ポリエチレンが広く用いられるように
なってきた。
However, polypropylene film is not suitable for general-purpose processing methods such as air-cooled inflation molding, and has the disadvantages of poor impact strength (especially low-temperature impact strength) and low-temperature heat sealability, so its application fields are limited. has been limited. Therefore, in the general-purpose film field, high-pressure low-density polyethylene and low-pressure high-density polyethylene, which are resins that compensate for these drawbacks, have come to be widely used.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかしながら、これ等樹脂は上記の欠点を補うには有効
であるが、透明性が劣る欠点を有している。
However, although these resins are effective in compensating for the above drawbacks, they have the drawback of poor transparency.

一方、線型のエチレン共重合体は、上記の汎用樹脂より
格段に良好な衝撃強度、低温衝撃強度および環境応力破
壊(E S CR)といった機械的強度やヒートシール
性ホットタック性等に優れた樹脂である。この共重合体
の高透明フィルムの成形法としては、良く知られたTダ
イ成形法および水冷インフレ成形法の外に、急冷させる
ニアリングを有した空冷インフレ成形法(例えば特開昭
53−146764)等の汎用加工法が知られている。
On the other hand, linear ethylene copolymers are resins with excellent mechanical strength such as impact strength, low-temperature impact strength, and environmental stress fracture (ESCR), as well as heat sealability and hot tack properties, which are much better than the general-purpose resins mentioned above. It is. In addition to the well-known T-die molding method and water-cooled inflation molding method, methods for molding a highly transparent film of this copolymer include an air-cooled inflation molding method with a near ring for rapid cooling (for example, Japanese Patent Application Laid-Open No. 146764-1983). General-purpose processing methods such as

ところが、これら成形法を用いて線型のエチレン共重合
体を単にフィルムに成形したのでは、フィルム透明性だ
けlは良好となるものの、フィルムのアンチブロッキン
グ性およびスリップ性の点から全く実用性のないものと
なってしまう。これながら、これでは透明性が不満足と
なってしまったり、各物性のバランスがとれないなどの
欠点が生じてしまう。
However, if a linear ethylene copolymer is simply molded into a film using these molding methods, although the film transparency is good, it is completely impractical in terms of the anti-blocking and slip properties of the film. It becomes a thing. However, this results in disadvantages such as unsatisfactory transparency and inability to maintain a balance between physical properties.

本発明は、これらの欠点を解消することを目的とするも
のであり、線型のエチレン共重合体の良い性質を保ちな
がら上記の諸品質のバランスを良好にしたものである。
The purpose of the present invention is to eliminate these drawbacks, and to improve the balance of the above-mentioned qualities while maintaining the good properties of linear ethylene copolymers.

〔問題点を解決するための手段〕[Means for solving problems]

すなわち本発明は、下記(a)〜(c)の各成分を含み
、(al成分100重量部に対し、(b)成分が0.0
1〜1重量部および(c1成分が0.01〜1重量部の
配合割合であることを特徴とする押出成形用樹脂組成物
である。
That is, the present invention includes each of the following components (a) to (c), and the component (b) is 0.0 parts by weight per 100 parts by weight of the Al component.
This is a resin composition for extrusion molding, characterized in that the blending ratio of the c1 component is 1 to 1 part by weight and 0.01 to 1 part by weight.

(a)  チーグラー系触媒を用いて製造された密度0
.910=0.940 g/crn” 、メルト7!:
l−1/ −)0.01〜20g/10分かつ共単量体
含量1〜10重量%のエチレン共重合体 (bl  平均粒径20μ以下のゼオライト(c)  
有機アミド化合物 本発明の組成物は、上記の点で優れているので、押出成
形品の中でも特にフィルムやラミネート材料に適してい
る。
(a) Density 0 produced using Ziegler catalyst
.. 910=0.940 g/crn”, Melt 7!:
l-1/-) 0.01 to 20 g/10 min and a comonomer content of 1 to 10% by weight ethylene copolymer (bl Zeolite (c) with an average particle size of 20 μ or less
Organic amide compound The composition of the present invention is excellent in the above points and is therefore particularly suitable for extrusion molded products, such as films and laminate materials.

〔作 用〕[For production]

本発明で用いられる上記(a)成分は、チーグラー系触
媒を用いて製造された密度0.910〜0.940g/
Cm3、メルトフローレート0.01〜20g/10分
かつ共単量体含量1〜10重量%のエチレン共重合体が
適する。
The above component (a) used in the present invention is produced using a Ziegler catalyst and has a density of 0.910 to 0.940 g/
Ethylene copolymers having a melt flow rate of 0.01 to 20 g/10 min and a comonomer content of 1 to 10% by weight are suitable.

好ましくは、密度0.915〜0.930 g/am’
、メルトフローレート0.1〜15g/10分かつ共単
量体含量2〜8重量%のものである。
Preferably, the density is 0.915 to 0.930 g/am'
, a melt flow rate of 0.1 to 15 g/10 minutes and a comonomer content of 2 to 8% by weight.

密度が上記範囲を下廻るものは、組成物にしたときのフ
ィルム等のブロッキング低下が大きくて本発明の効果が
低く、また範囲を上廻るものは、透明性や衝撃強度が悪
化するといった欠点を存する。
If the density is below the above range, the blocking of the film or the like when made into a composition will be greatly reduced and the effect of the present invention will be low, and if the density is above the range, there will be disadvantages such as poor transparency and impact strength. Exists.

、また、メルトフローレートが上記範囲を下廻るものは
、加工性が悪く、上廻るものは、加工性及びフィルム等
の衝撃強度が低下する欠点を有する。
Also, those with a melt flow rate below the above range have poor processability, and those with a melt flow rate above the above range have the disadvantage of reduced processability and impact strength of the film, etc.

また、共単量体含量が上記範囲をはずれるものは、最終
目的の組成物の透明性、衝撃強度、剛性の点で好ましく
ないといった欠点を有する。
Furthermore, comonomer contents outside the above range have disadvantages such as undesirable clarity, impact strength, and rigidity of the final target composition.

さらに好ましくは、フローレーシオが6〜15であるも
のが、押出加工性や透明性の点で望ましい。
More preferably, those having a flow ratio of 6 to 15 are desirable in terms of extrusion processability and transparency.

このような共重合体は、エチレンと、共重合体としてプ
ロピレン、ブテン−1、ヘキセン−1,4−メチルペン
テン−11オクテン−1等の1種または2種以上を圧カ
フ、Qkg/cm”程度以下で重合して得られるもので
、製造法としては、例えば特公昭56− 18132等
の公報に記載された方法が知られている。
Such a copolymer is produced by combining ethylene with one or more copolymers such as propylene, butene-1, hexene-1,4-methylpentene-11-octene-1, etc., using a pressure cuff, Qkg/cm. It is obtained by polymerizing at a low temperature, and the method described in Japanese Patent Publication No. 56-18132 is known as a manufacturing method.

本発明で用いる上記山)成分は、平均粒径20μ以下、
好ましくは5μ以下のゼオライトである。
The above-mentioned component (top) used in the present invention has an average particle size of 20 μm or less,
Preferably it is a zeolite with a diameter of 5μ or less.

20μより大きなものはフィルムの外観を阻害する。Anything larger than 20μ will impair the appearance of the film.

ゼオライトは、天然のものでも合成のものでも差し支え
ない。例えば、C3100(日本化学工業社製商品名)
やU47(水沢化学社製商品名)がある。
The zeolite may be natural or synthetic. For example, C3100 (product name manufactured by Nihon Kagaku Kogyo Co., Ltd.)
and U47 (trade name manufactured by Mizusawa Chemical Co., Ltd.).

更に、本発明で用いる上記(c1成分は、有機アミド化
合物である。好ましい具体例に、不飽和脂肪酸アミド、
飽和脂肪酸アミドがある。
Furthermore, the above (c1 component) used in the present invention is an organic amide compound. Preferred specific examples include unsaturated fatty acid amide,
Contains saturated fatty acid amides.

これらの(al〜(c)成分の配合割合は、(al成分
100重量部に対し、(bl成分が0.01〜1重量部
、好ましくは0.1〜0.6重量部であり、および(c
)成分が0.01〜1重量部、好ましくは0.05〜0
.3重量部である。
The mixing ratio of these components (al to (c)) is such that the (bl component is 0.01 to 1 part by weight, preferably 0.1 to 0.6 part by weight, per 100 parts by weight of the (al component), and (c
) component is 0.01 to 1 part by weight, preferably 0.05 to 0
.. It is 3 parts by weight.

(bl成分の量が上記の範囲を下廻ると、フィルムにし
たときのブロッキング性が悪化して好ましくなく、上廻
るとフィルムにしたときの透明性が著しく低下する。
(If the amount of the BL component is less than the above range, the blocking property when formed into a film will deteriorate, which is undesirable; if it exceeds the above range, the transparency when formed into a film will decrease significantly.

(c)成分が上記範囲を下廻ると、スリップ性、ブロッ
キング性が著しく低下し、上廻るとスリップしすぎるば
かりでなく、印刷性やヒートシール性が著しく悪化して
好ましくない。
If component (c) is below the above range, the slip properties and blocking properties will be significantly reduced, and if it is above the range, not only will there be too much slip, but the printability and heat sealability will also be significantly deteriorated, which is undesirable.

透明性、ブロッキング性、スリップ性のバランスをこと
さら満足行くものにするには、好ましくは、これら組成
物を製造する過程で、(a)成分として200μ以下の
顆粒状のものを使用し、まず(a)成分と(bl成分と
をヘンシェルミキサー等のブレンダーで良く混合し、こ
の混合物に(c)成分を更に添加して混合したものを押
出機でペレタイズすると言った順序で製造した組成物を
使用することが望ましい。
In order to achieve a particularly satisfactory balance of transparency, blocking properties, and slip properties, preferably, in the process of producing these compositions, granules with a size of 200 μm or less are used as component (a), and first ( Use a composition produced in the following order: Component a) and BL component are thoroughly mixed with a blender such as a Henschel mixer, and component (c) is further added to this mixture and the mixed mixture is pelletized with an extruder. It is desirable to do so.

ブロッキング性、スリップ性、透明性、印刷性のバラン
スをことさら満足の行くものにするには、(c)成分と
して不飽和脂肪酸アミドに飽和脂肪酸アミドを3:1近
傍に混合したものを、上記製造法でペレタイズした組成
物が、特に望ましい。不飽和脂肪酸アミドとしてはエル
シン酸アミド、オレイン酸アミド等、飽和脂肪酸アミド
としてはベヘニン酸アミド、ステアリン酸アミド等が好
ましい。
In order to achieve a particularly satisfactory balance of blocking properties, slip properties, transparency, and printability, a mixture of unsaturated fatty acid amide and saturated fatty acid amide in a ratio of about 3:1 as component (c) is used in the above-mentioned production process. Particularly desirable are compositions that are pelletized by a process. Preferred unsaturated fatty acid amides include erucic acid amide and oleic acid amide, and preferred saturated fatty acid amides include behenic acid amide and stearic acid amide.

本発明においは、通常使用される酸化防止剤、安定剤、
防曇剤、帯電防止剤、UV剤、核剤等の安定剤を配合し
てもよい。
In the present invention, commonly used antioxidants, stabilizers,
Stabilizers such as antifogging agents, antistatic agents, UV agents, and nucleating agents may be added.

また(al成分としては、上記共重合体のみならず、上
記共重合体に高圧法低密度ポリエチレン、高密度ポリエ
チレン、ポリプロピレン、ポリブテン、エチレン酢酸ビ
ニル共重合体等の他の樹脂とのブレンド物も適用できる
。また、タルクを、(b)成分のゼオライトとの合計量
で(a)成分100重量部に対して1重量部以下併用す
るとブロッキングが良好となり、吸湿による発泡現象も
生じることなく、好ましい。
(Al components include not only the above-mentioned copolymers, but also blends of the above-mentioned copolymers with other resins such as high-pressure low-density polyethylene, high-density polyethylene, polypropylene, polybutene, and ethylene-vinyl acetate copolymers). It is also possible to apply talc in combination with the zeolite component (b) in a total amount of 1 part by weight or less per 100 parts by weight of component (a), which is preferable because blocking is good and no foaming phenomenon occurs due to moisture absorption. .

〔発明の効果〕〔Effect of the invention〕

本発明で得られた組成物を用いたフィルム等は、透明性
に優れ、スリップ性、印刷性のバランスが良好かつブロ
ッキング性が実用域にあるものである。
Films using the composition obtained in the present invention have excellent transparency, a good balance between slip properties and printability, and blocking properties that are within the practical range.

〔実施例〕〔Example〕

後に記した第1表中にあげた配合成分のうち、(al、
 (b)およびその他の成分をヘンシェルミキサーで混
合し、これに(c1成分を更に添加して混合したものを
、スクリュー径35寵でL/D 28の押出機にて、温
度230℃でペレタイズして組成物を作った。
Among the ingredients listed in Table 1 below, (al,
(b) and other components were mixed in a Henschel mixer, and the mixture was further added with component (c1) and pelletized at a temperature of 230°C in an extruder with a screw diameter of 35 mm and L/D 28. A composition was prepared.

この組成物を用いて、次の三種類の方法でフィルムに加
工した。
This composition was processed into films using the following three methods.

(i)フィルム加工法(11 組成物を一重エアスリットエアリングを用いた線型エチ
レン重合体用空冷インフレーション押出機(40mm径
、スクリューL/D 18)及びスパイラル型グイ75
1層径(リップ幅3龍)を用い、200℃でフィルム厚
み30μに押出す。この時、ブロー比は2.0に調整し
た。
(i) Film processing method (11) A linear air-cooled inflation extruder for ethylene polymer using a single air slit air ring (40 mm diameter, screw L/D 18) and a spiral type Gui 75
Using 1 layer diameter (lip width 3 times), extrude at 200°C to a film thickness of 30μ. At this time, the blow ratio was adjusted to 2.0.

(ii )フィルム加工法(2) 組成物を二重エアスリ・ノドニアリンク゛を用し)で、
上記空冷インフレーションと同様に行なう。
(ii) Film processing method (2) The composition is processed using a double air sliver nodonia link.
Perform the same procedure as for the air cooling inflation above.

(iii )フィルム加工法(3) 組成物を一重エアスリットエアリンク゛を用6”=た空
冷インフレーション押出機(40寵径、スクリューL1
022)及びスパイラル型ダイ1001m径(リップ幅
0.8mm)を用い、180℃でフィルム厚み30μに
押出す。この時、ブロー比を1.5に調整した。
(iii) Film processing method (3) The composition was passed through an air-cooled inflation extruder (40 diameter, screw L1) using a single air slit air link.
022) and a spiral die with a diameter of 1001 m (lip width 0.8 mm) at 180° C. to a film thickness of 30 μm. At this time, the blow ratio was adjusted to 1.5.

このようにして得たフィルムの品質を以下の項目につい
て評価した。測定法は次の通りである。
The quality of the film thus obtained was evaluated on the following items. The measurement method is as follows.

評価結果は、第2表の通りである。The evaluation results are shown in Table 2.

なお、メルトフローレート(MFR)は、ASTMD1
238  (190℃)により、またフローレーシオは
、JIS  K7210−1975により、メルトイン
デクサ−で190℃下、次の式に基ずいて求めた。
The melt flow rate (MFR) is based on ASTM D1.
238 (190°C), and the flow ratio was determined according to JIS K7210-1975 using a melt indexer at 190°C based on the following formula.

また、シリカ、ゼオライトやタルクの平均粒径は、コー
ルタ−カウンター法(分散方法は、28KC超音波5分
間、0.01%へキサメタリンリン酸ソーダによる)に
て求めた数値である。
The average particle diameters of silica, zeolite and talc are values determined by the Coulter Counter method (dispersion method is 28KC ultrasonic wave for 5 minutes, using 0.01% sodium hexametaline phosphate).

合成シリカはサイロイド66、ゼオライトはC8100
を用いた。
Synthetic silica is Thyroid 66, and zeolite is C8100.
was used.

(1)ヘイズ ASTM  D1003−61に準拠して測定。(1) Haze Measured in accordance with ASTM D1003-61.

(2)光散乱指数(LSI) 成形フィルムを23℃±2℃、50±5%RHに24時
間以上状り、調節後、LSI計EvanceElect
roselenium社製)にて、光散乱指数を測定す
る。
(2) Light scattering index (LSI) The formed film was kept at 23°C ± 2°C and 50 ± 5% RH for more than 24 hours, and after adjustment, the LSI meter EvanceElect
(manufactured by Roselenium) to measure the light scattering index.

(3)ブロッキング 成形フィルムを高温(45℃)、高荷重(50g/c+
++”)下で24時間フィルム密着性を促進させた後、
ショツパー型引張試験機にて引張速度500 m/mi
nの条件でフィルム接着面10e11”を剪断的に引き
剥がすに要する最大応力(g/locmz)で示す。
(3) Blocking molded film at high temperature (45℃) and high load (50g/c+
After promoting film adhesion for 24 hours under
Tensile speed 500 m/mi using Schopper type tensile testing machine
It is expressed as the maximum stress (g/locmz) required to shearly peel off the film adhesive surface 10e11'' under conditions of n.

(4)静摩擦係数 ASTM  D1894に準拠して測定。(4) Static friction coefficient Measured in accordance with ASTM D1894.

(5)濡れ張力 ASTM  D2578−67に準拠して測定。(5) Wetting tension Measured in accordance with ASTM D2578-67.

(以下余白)(Margin below)

Claims (1)

【特許請求の範囲】 下記(a)〜(c)の各成分を含み、(a)成分100
重量部に対し、(b)成分が0.01〜1重量部および
(c)成分が0.01〜1重量部の配合割合であること
を特徴とする押出成形用樹脂組成物。 (a)チーグラー系触媒を用いて製造された密度0.9
10〜0.940g/cm^3、メルトフローレート0
.01〜20g/10分かつ共単量体含量1〜10重量
%のエチレン共重合体 (b)平均粒径20μ以下のゼオライト (c)有機アミド化合物
[Claims] Contains each of the following components (a) to (c), 100% of component (a)
A resin composition for extrusion molding, characterized in that component (b) is blended in a proportion of 0.01 to 1 part by weight and component (c) is blended in a proportion of 0.01 to 1 part by weight based on parts by weight. (a) Density 0.9 produced using Ziegler catalyst
10~0.940g/cm^3, melt flow rate 0
.. Ethylene copolymer with a comonomer content of 01 to 20 g/10 minutes and a comonomer content of 1 to 10% by weight (b) Zeolite with an average particle size of 20 μ or less (c) Organic amide compound
JP61099796A 1986-04-30 1986-04-30 Resin composition for extrusion molding Granted JPS61281142A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61099796A JPS61281142A (en) 1986-04-30 1986-04-30 Resin composition for extrusion molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61099796A JPS61281142A (en) 1986-04-30 1986-04-30 Resin composition for extrusion molding

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP13303582A Division JPS5922944A (en) 1982-07-30 1982-07-30 Resin composition for extrusion molding

Publications (2)

Publication Number Publication Date
JPS61281142A true JPS61281142A (en) 1986-12-11
JPS648018B2 JPS648018B2 (en) 1989-02-10

Family

ID=14256870

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61099796A Granted JPS61281142A (en) 1986-04-30 1986-04-30 Resin composition for extrusion molding

Country Status (1)

Country Link
JP (1) JPS61281142A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS636037A (en) * 1986-06-26 1988-01-12 Idemitsu Petrochem Co Ltd Polyethylene resin composition
US5346944A (en) * 1990-12-21 1994-09-13 Sumitomo Chemical Company, Limited Polyolefin resin composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6199797A (en) * 1984-10-22 1986-05-17 株式会社 テイエルブイ Disk type steam trap

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6199797A (en) * 1984-10-22 1986-05-17 株式会社 テイエルブイ Disk type steam trap

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS636037A (en) * 1986-06-26 1988-01-12 Idemitsu Petrochem Co Ltd Polyethylene resin composition
US5346944A (en) * 1990-12-21 1994-09-13 Sumitomo Chemical Company, Limited Polyolefin resin composition

Also Published As

Publication number Publication date
JPS648018B2 (en) 1989-02-10

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