JPS5998147A - Polyolefin composition - Google Patents

Polyolefin composition

Info

Publication number
JPS5998147A
JPS5998147A JP20730482A JP20730482A JPS5998147A JP S5998147 A JPS5998147 A JP S5998147A JP 20730482 A JP20730482 A JP 20730482A JP 20730482 A JP20730482 A JP 20730482A JP S5998147 A JPS5998147 A JP S5998147A
Authority
JP
Japan
Prior art keywords
film
feldspar
silica
acid amide
density polyethylene
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
JP20730482A
Other languages
Japanese (ja)
Other versions
JPH0149302B2 (en
Inventor
Yoshio Matsumoto
良雄 松本
Toshio Fujii
敏雄 藤井
Koichi Hasegawa
幸一 長谷川
Iwao Seki
関 巌
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 Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP20730482A priority Critical patent/JPS5998147A/en
Publication of JPS5998147A publication Critical patent/JPS5998147A/en
Publication of JPH0149302B2 publication Critical patent/JPH0149302B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:A composition for molding a film, not causing blocking even by film molding through guenching, obtained by blending a polyolefin resin with finely divided silica, finely divided feldspar as fillers and a fatty carboxylic acid amide as lubricant in specific amounts, respectively. CONSTITUTION:A polyolefin resin (preferably linear low-density polyethylene) is blended with 0.05-1wt%, preferably 0.1-0.8wt% finely divided silica(preferably 3-8mu average particle diameter) and 0.05-1wt%, preferably 0.1-0.8wt% finely divided feldspar as fillers and 0.01-0.5wt%, preferably 0.05-0.2wt% fatty carboxylic acid amide(preferably unsaturated fatty acid amide such as oleic amide, etc.), to give the desired composition. EFFECT:A film having improved transparency is obtained.

Description

【発明の詳細な説明】 本発明はポリオレフィン組成物に閃する。詳しくはフィ
ルムを成形するに用いて好適なポリオレフィン組成物に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to polyolefin compositions. Specifically, the present invention relates to a polyolefin composition suitable for use in forming a film.

従来よシ、ポリオレフィン樹脂f脂は錘々の用途に多用
されておシ、特にフィルムは、わl々の物品の包装用累
材として広く用いられている。
Conventionally, polyolefin resins have been widely used for weight applications, and in particular, films have been widely used as packaging materials for everyday articles.

ポリオレフィン樹脂+脂を用いてフィルムを製造する方
法は例えばTダイ成形、インフレーション成形等が多く
用いられており、特に袋状の成形品を得ようとする場合
に筒状で押し出すインフレーション成形が便利なため多
用されている。
For example, T-die molding, inflation molding, etc. are often used to manufacture films using polyolefin resin + fat, and inflation molding, which extrudes in a cylindrical shape, is especially convenient when trying to obtain a bag-shaped molded product. It is often used for this reason.

インフレーション成形等によシフイルムを成形する場合
フィルムを透明にするためにはダイから押出されたフィ
ルムを水等の冷媒を用いて急冷することが行なわれてb
る。
When forming a film by inflation molding etc., in order to make the film transparent, the film extruded from the die is rapidly cooled using a coolant such as water.
Ru.

し力)シ、この急冷によりフィルムを透明にすると、得
られたフィルムの表面が平滑とカシ、密度も低下するの
でフィルムの腰か弱くなる(剛性が低下する)。この結
果シリカ等の添加剤を若干配合してもフィルム表面を凹
凸とすることができず、むしろ添加剤はフィルム内部に
取り込まれてしまいフィルム同志が密着現象(ブロッキ
ング)すなわち、筒状のフィルムを偏平に押しつぶし密
着させた場合や、一枚のフィルムをロール状に巻回した
場合にフィルム同志がくっついてしまい剥れなくなる現
象、を起し例えば袋とした場合の開口性が恋〈なp実用
上大変不都合であった。
When the film is made transparent by this rapid cooling, the surface of the resulting film becomes smooth and stiff, and the density also decreases, making the film less stiff (reduced rigidity). As a result, even if a small amount of additives such as silica are added, the surface of the film cannot be made uneven; instead, the additives are incorporated into the film, causing the films to adhere to each other (blocking), or forming a cylindrical film. When flattened and pressed together, or when a single film is wound into a roll, the films stick together and cannot be peeled off. It was extremely inconvenient.

本発明者等は上述のようなポリオレフィン樹脂の欠点を
解消するべく、独々検剖を重ねた結果、ポリオレフィン
樹脂に2釉の特定の勲侵質充填剤を併用配合し、さらに
特定の滑剤を配合、することによシ、急冷によるフィル
ム成形を行なってもブロッキングを起さず−且つ透明性
にすぐれたフィルムが得られることを見出し、本発明を
完成するに至った。
In order to eliminate the above-mentioned drawbacks of polyolefin resin, the inventors of the present invention have conducted autopsies on their own and have combined two glazes of specific erosive fillers with polyolefin resin, and also added a specific lubricant. The present inventors have discovered that by blending, a film with excellent transparency can be obtained that does not cause blocking even when film is formed by rapid cooling, and the present invention has been completed.

す々わち、本発明の少旨はポリオレフィン樹脂中に微粉
状シリカをθ、Oj〜/ in 量%、微粉状長石を0
.05〜7重量%、脂肪族カルボン酸アミドを0.0/
−0,3重量%配合させてなるポリオレフィン組成物に
存する。
In other words, the gist of the present invention is to add fine powder silica to a polyolefin resin by θ, Oj~/in amount%, and fine powder feldspar to 0%.
.. 05-7% by weight, aliphatic carboxylic acid amide 0.0/
-0.3% by weight of the polyolefin composition.

本発明に用込るポリオレフィン樹脂とは、高密度ポリエ
チレン、低密度ポリエチレン、線状低密度ポリエチレン
、ポリプロピレン、エチレン−プロピレン共重合体、ポ
リブテン−/、エチレン−酢酸ビニル共重合体等であり
、特に密度θ、りθl〜θ、タグθft’/dの中低密
度ポリエチレン、線状低密度ポリエチレンが好適であシ
、中でも線状低密度ポリエチレンが最適である。
The polyolefin resin used in the present invention includes high density polyethylene, low density polyethylene, linear low density polyethylene, polypropylene, ethylene-propylene copolymer, polybutene/, ethylene-vinyl acetate copolymer, etc. Suitable are medium-low density polyethylene and linear low-density polyethylene with a density θ, θl to θ, and a tag θft'/d, with linear low-density polyethylene being most suitable.

線状低密度ポリエチレンきはエチレント他のα−オレフ
ィンとの共重合物であり、従来の高圧法によシ製造され
た低密度ポリエチレンhh Jllとは異なる。線状低
密度ポリエチレンは、例工はエチレンと、他のα−オレ
フィンとしてブテン、ヘキセン、オクテン、デセン等と
の共1合体であり、中低圧法高苦度ポリエチレン製造に
用いられるチーグラー弗触謀又はフィリップヌ型触媒を
用いて製造されたものであり、従来の高密度ポリエチレ
ンを共1合によシ短かb枝分かれ構造とし、密度もとの
短鎖枝分かれを利用して適当に低下させθ、り/〜O9
り、;tsy/ctA程度としたものであり、従来の低
密度ポリエチレンより@鎖性があシ、高密度ポリエチレ
ンより枝分かれが多い構造のポリエチレンである。
Linear low-density polyethylene is a copolymer of ethylene and other α-olefins, and is different from low-density polyethylene hh Jll produced by conventional high-pressure methods. Linear low-density polyethylene is a combination of ethylene and other α-olefins such as butene, hexene, octene, decene, etc., and is a Ziegler compound used in the production of high-bitterness polyethylene by a medium-low pressure method. Alternatively, it is produced using a Philippe type catalyst, in which conventional high-density polyethylene is made into a short or b-branched structure by combining, and the density is appropriately lowered by utilizing the original short chain branching. ,ri/~O9
tsy/ctA, and is a polyethylene with a structure that is more chain-like than conventional low-density polyethylene and more branched than high-density polyethylene.

このようなポリオレフィン樹脂に併用配合される無機質
充填剤は微粉状のシリカと長石である。
The inorganic fillers that are blended together with such polyolefin resins are finely powdered silica and feldspar.

微粉状シリカは二酸化ケイ紫(5in2)を主成分とす
る略球形の微粉状を呈するものであり、天然に産するも
のと人工的に合成されるものがある。
Powdered silica is a roughly spherical fine powder whose main component is purple silicon dioxide (5in2), and there are naturally occurring types and artificially synthesized types.

本発明において使用するシリカは天然シリカでも合成シ
リカでも良い〃ぺ平均粒径が/〜10μ、好1しくは3
〜rμのものが望ましい。シリカの平均粒径がこれ以上
小さいと畝条を起し樹脂中での分散性が悪くなシ、首た
突気中に浮遊し易く力るので環境衛生上問題があり、こ
れ以上大きくなるとポリオレフィンに配合してフィルム
に成形した後ゲル化してしまいフィルムの外観が不良と
なるので使用でき々い。
The silica used in the present invention may be natural silica or synthetic silica, and has an average particle size of /~10μ, preferably 3
~rμ is desirable. If the average particle size of silica is smaller than this, it will cause ridges and its dispersibility in the resin will be poor, and it will easily float in the air and cause stress, causing environmental hygiene problems.If it becomes larger than this, polyolefin After being mixed into a film and formed into a film, it gels and the film has a poor appearance, making it unsuitable for use.

シリカの配合量はポリオレフィン硝脂中にθ、θ!〜/
重量先、好甘しくはO0/〜θ、♂重量%であり、これ
以上少々ければブロッキング防止効果を生起せず、すな
わち、袋とした場合の開口性が悪くなシ、これ以上多い
とフィルムの透明性が損われる。
The amount of silica in the polyolefin resin is θ, θ! ~/
In terms of weight, it is preferably O0/~θ, ♂% by weight; if it is a little more than this, the blocking prevention effect will not occur, that is, if it is made into a bag, the opening property will be poor, and if it is more than this, the film will be damaged. transparency is impaired.

微粉状長石はカルシウム(Ca)sナトリウム(Na 
)、カリウム(K)々どのアルミノケイ酸塩を主成分と
する略平板状の微粉状を呈するものであり、成分によっ
てjカリ長石、ソウ投石、灰是石、斜長石等の柚知に分
けられるが、通常はこれらの混合物である。本発明にお
いて使用する長石は上述のような混合状態のもので良く
、その各種の長石の割合は任慧であって良いが、平均粒
径が7〜/θμ、好1しくは3〜lμのものが良い。
Fine powder feldspar is composed of calcium (Ca)sodium (Na
), potassium (K), and other aluminosilicate as the main components, and is in the form of a roughly tabular fine powder, and is divided into sulfurs such as potassium feldspar, sourstone, scourite, plagioclase, etc. depending on the composition. However, it is usually a mixture of these. The feldspar used in the present invention may be in a mixed state as described above, and the proportion of each type of feldspar may be determined as desired, but the average particle size is 7-/θμ, preferably 3-1μ. Things are good.

長石の平均粒径の測定は長石は上述したように平板状を
呈するものであるため、厚さは考慮せず、顕微鏡で観察
し、七〇長辺と短辺の平均値を求め、これを平均粒径と
した。
To measure the average particle size of feldspar, as mentioned above, feldspar is tabular, so without considering the thickness, it is observed with a microscope, and the average value of the long side and short side is calculated. It was taken as the average particle size.

長石の平均粒径が上記の範囲を外れるとシリカの場合と
同様の欠陥を生じ好ましくない。
If the average grain size of feldspar is outside the above range, it is not preferable because it causes defects similar to those of silica.

長石の配合量はポリオレフィン側脂中にθ、O!〜/重
景%、t重量ましくはo、i〜OI JL!祈%であシ
、これ以上少なければブロッキング防止効果を生起せず
、これ以上多いとフィルムの透明性が損われる。
The amount of feldspar contained in the polyolefin side fat is θ, O! ~/weight %, t weight or o, i~OI JL! However, if the amount is less than this, the anti-blocking effect will not occur, and if it is more than this, the transparency of the film will be impaired.

上述したシリカと長石の併用と共に用いられる特定の滑
剤としては脂肪族カルボン酸アーミドが用いられる。脂
肪族カルボン酸アミドとしては融点が50〜770℃好
ましくは70〜りθる。例えばオレイン隘アミド(融点
(MP)ニア!℃)、エルシン酸アミド(MP :と0
℃)、リシノール酸アミド(up:crc)、エルク酸
アミド(MP : 7♂〜♂/r)、)、ステアリン酸
アミド(MP:/θθ℃)、オキシステアリン酸アミド
(MP : 10sr: )、メチロール酸アミド(M
P:102℃)等を挙げることができる。融点が770
℃以上であるとフィルムに成形した場合に、フィルム表
面にブリードしてくる速度が遅くなりすき゛、フィルム
に良好なflを性を付与せず彪にした場合の開口性に寄
与し細い。融点が!θ℃以下であると、ブリードしすぎ
1例えば成形時に引取ロール等の表面に付光してフィル
ムに転写し、透明性不良の原因になるしべとついた感触
を与える等の問題かある。
Aliphatic carboxylic acid amide is used as a specific lubricant used in conjunction with the above-mentioned combination of silica and feldspar. The aliphatic carboxylic acid amide has a melting point of 50 to 770°C, preferably 70 to θ. For example, oleic acid amide (melting point (MP) near! °C), erucic acid amide (MP: and 0
℃), ricinoleic acid amide (up: crc), erucic acid amide (MP: 7♂~♂/r), ), stearic acid amide (MP: /θθ℃), oxystearic acid amide (MP: 10sr: ), Methylolic acid amide (M
P: 102°C). Melting point is 770
If the temperature is higher than 0.degree. C., the speed at which the film bleeds onto the surface of the film will be slow when it is formed into a film, and it will contribute to the aperture of the film when it is not imparted with properties and is made narrower. The melting point! If the temperature is below θ°C, there may be problems such as excessive bleeding (1), for example, when light is applied to the surface of the take-up roll during molding and transferred to the film, giving a sticky feel that causes poor transparency.

脂肪族カルボン酸アミドの配合−JU−け通常0.0/
〜O,S重量%、好ましくはθ、θS〜θ、21お%で
あシ、これ以上少なげればフィルムに良好な滑性を付与
し得す、これ以上多ければ、ブリードしすぎ上述と同行
の欠陥を生起する。
Blend of aliphatic carboxylic acid amide - JU - usually 0.0/
~O, S weight%, preferably θ, θS ~ θ, 21%. If it is less than this, good lubricity can be imparted to the film. If it is more than this, it will cause excessive bleeding and the above-mentioned problem. Give rise to accompanying defects.

本発明の組成物を用込てフィルム成形を行なツPc ’
M 合s フィルムのブロッキングが良好に防止し得る
理由は完全に解明されてはbないが概路次のような理由
によるものと考えられる。
Forming a film using the composition of the present invention Pc'
Although the reason why the blocking of the M compound film can be effectively prevented has not been completely elucidated, it is thought to be due to the following reasons.

シリカと長石は、その各々は仙腸の充填剤として用いら
れてbる。しかし、これらの物質を各々樹脂に添加して
も、それ)1どのブロッキング防止効果は得られない。
Silica and feldspar are each used as sacroiliac fillers. However, even if each of these substances is added to the resin, no anti-blocking effect can be obtained.

これは、シリカは前述したように略球形の形状を呈する
ため、これによってフィルム表面に形成される凹凸が比
戟的均−でなだらかな凹凸であるためと考えられ、また
長石は前述したように略平板状の形状を呈スルタめフィ
ルム成形時に、フィルムが溶融延伸等の操作を受けると
フィルム表面と略平行に並んでしまいフィルム表面にほ
とんど凹凸を形成しないためと考えられる。Lカ)るに
Qrにの平均粒径を有するシリカと長石とを併用して仙
腸に配合すると、略球形のシリカが長石の間に入シ込み
、フィルムが、溶融延伸等の操作を受けても長石がフィ
ルム表面と略平行に廉ぷこ七を阻止するので、フィルム
表面にシリカと長石による凹凸が極めて多数形成され、
フィルムのブロッキングが良好に防止し得るものと考え
られる。
This is thought to be because silica has a roughly spherical shape as mentioned above, so the unevenness formed on the film surface is relatively uniform and smooth, and feldspar has a roughly spherical shape. This is thought to be because when the film is formed into a substantially flat plate-like shape, when the film is subjected to an operation such as melt-stretching, the film lines up substantially parallel to the film surface, and almost no irregularities are formed on the film surface. When silica and feldspar having an average particle size of However, since the feldspar is approximately parallel to the film surface and prevents it from collapsing, an extremely large number of irregularities due to silica and feldspar are formed on the film surface.
It is considered that blocking of the film can be effectively prevented.

本発明の組成物は上述のように、フィルム表面に細かな
多数の凹凸を形成させブロッキングを防止するものであ
シ、比較的薄肉の、例えば!θμ以下、好ましくはグO
μ以下の厚さのフィルムを製造するのに用いて大変効果
的である。
As mentioned above, the composition of the present invention prevents blocking by forming a large number of fine irregularities on the surface of the film. θμ or less, preferably guO
It is very effective when used to produce films with a thickness of less than μ.

次姉実施例により本発明を更に詳細に、説明するが、本
発明はその要旨を越えない限シ以下の実施例に限定され
るものではない。
The present invention will be explained in more detail with reference to the following embodiments, but the present invention is not limited to the following embodiments unless the gist thereof is exceeded.

実施例中、透明性についてはJ工5K−67/¥に準拠
しくもシ価(Haze ) (九)を測定し、〈もシ価
がQj%以下のものを〔○〕、くもり価がグ、!〜t、
717%のものを〔△〕、<もシ価が6%以上のものを
〔×〕と評価した。
In the examples, regarding transparency, the haze value (9) was measured in accordance with J Engineering 5K-67/¥, and the haze value was Qj% or less [○], the haze value was G, ! ~t,
Those with a value of 717% were evaluated as [△], and those with a value of 6% or more were evaluated as [x].

また、開口性については、得られたフィルムをヒートシ
ールすることによシ製袋し、その後この袋の任意の位置
から/ 、2 cm X / Ocmの2枚に重なった
試験片を切り出し、この試験片を20℃(相対湿度60
%)の恒温室に72時間放置し、次いでこの試験片の長
手方向両端部を1m幅で剥離し、接着面/ OcnlX
 / 0 >の試験片とする。剥離した四枚のフィルム
端部を夫々チャックに固定し、フィルムを引剥す方向に
チヤツクを移動速度30mm1分で移動させ、この際の
フィルムが引豹1される最大強度(2//θ0d)を得
、この値が! Of// 00 cr!以下のものを〔
○〕、jθ〜/ 00 f / cJのものを〔△〕、
/θ09//θOcr1以上のものを〔×〕と評価した
Regarding the openability, the obtained film was made into a bag by heat-sealing, and then two overlapping test pieces of 2 cm x 2 cm were cut out from any arbitrary position of the bag. The test piece was heated to 20°C (relative humidity 60°C).
%) in a constant temperature room for 72 hours, and then peeled off both longitudinal ends of this test piece in a 1 m width to form an adhesive surface/OcnlX.
/ 0 > test piece. The ends of the four peeled films were each fixed to a chuck, and the chuck was moved in the direction of peeling the film at a moving speed of 30 mm 1 minute, and the maximum strength (2//θ0d) at which the film was pulled was Get this value! Of// 00 cr! The following [
○], jθ~/00 f/cJ [△],
/θ09//θOcr1 or more was evaluated as [x].

笑カm例/〜グ、比較例7〜3 線状低密度ポリエチレン(メルトインデックス(/り0
℃): / 1710分、密度二θ、り/ざ9/crl
、共連合成分ニブテン−/、共1合成分量:/θ丘量%
)に第7表に示した通りの添加剤を配合し、Tダイ押出
様(住友恵+々械工業6り製、りθρ押出払に幅クタo
mm、クリアランス、/關のTダイを取シ付けたもの)
を用い収」脂温260℃、スクリュー回転i j Or
、p、m、、押出量26 kfl/hr、で下向きに押
出し、Tダイ直下/θcnlの位置に設けられた水憎(
水温−0℃)で急冷しつつ3θin / mi nの速
度で引取り、厚さ3jμのフィルムを得た。
Laughter Example/~G, Comparative Examples 7-3 Linear low-density polyethylene (melt index (/0)
°C): / 1710 minutes, density 2θ, ri/za 9/crl
, co-association component nibten-/, co-1 synthesis component amount: /θ hill amount %
) with the additives shown in Table 7, and the T-die extrusion type (manufactured by Sumitomo Megumi + Yoshiki Kogyo 6, and the width of the extrusion die θρ).
mm, clearance, / with T-die installed)
Fat temperature 260℃, screw rotation i j Or
, p, m,, extrusion downward at an extrusion rate of 26 kfl/hr, and a water hole (
While quenching at a water temperature of -0°C, the film was taken at a speed of 3θin/min to obtain a film with a thickness of 3jμ.

得られたフィルムの透明性及び開口性を評価し第1表に
示した。
The transparency and openness of the obtained film were evaluated and shown in Table 1.

カお、実施例及び比較例において「シリカA」は、平均
粒子径:りμ、表面積:220靜/ yrのシリカ(富
士テヴイソン■製、商品名:サイロイド#72)であり
、[シリカBJは、平均粒子径:3.3μ、表面at 
: 300n?/ frのシリカ(富士デヴイソン■製
、商品名:サイロイド4(−za<t)であり、「長石
」とは平均粒子径ニゲ、!μ、表面積:1.グの長石(
白石カルシウム■製、商品名:ミネツクス7)であり、
エルク彪アマイドは日本化成■社製、部品名:ダイヤミ
ッドL2θOである。(以下の実施例、比較例において
も同様) 第1表 注:配合量は全て重量%である。
In the Examples and Comparative Examples, "Silica A" is a silica (manufactured by Fuji Tevison ■, trade name: Thyroid #72) with an average particle diameter of 1 μm and a surface area of 220 m/yr, and [Silica BJ is , average particle size: 3.3μ, surface at
: 300n? / fr silica (manufactured by Fuji Davison ■, product name: Thyroid 4 (-za < t), "feldspar" refers to feldspar with an average particle size of 1.μ, surface area: 1.g
Manufactured by Shiraishi Calcium ■, product name: Minetsu 7),
Elk Biao Amide is manufactured by Nippon Kasei ■, part name: Diamid L2θO. (The same applies to the following Examples and Comparative Examples) Table 1 Note: All compounding amounts are weight %.

実施例!〜2、比較例グ 線状低密度ポリエチレン(メルトインデックス(/り0
℃): / yZio分、密g : 0.9.2/ f
/cIIr、共及合成分ニブテンー11共皿合成分量二
/θ友址%)に第−表に示した通シの添加剤を配合し、
インフレーション成形様(■フラコー社製!θβ押出機
に径/θ0關、スリト間隙/mmの塊状スリットを有す
るインフレーションダイを取り付けたもの)を用い側脂
温λθθ℃、スクリュー回転数j 60 r、p、m、
、押出@ 2 / kg/hr0、ブローアツプ比/、
!で下向きに押出し、ダイス直下、20儒の位置に筒状
フィルムの外側に沿って冷却水(20℃)を流下する冷
却リングを設け、これで急冷しっつ3θm / min
の速度で引取シ、厚さZθμのフィルムを得た。
Example! ~2, Comparative Example Linear low density polyethylene (melt index (/) 0
°C): / yZio min, density g: 0.9.2/f
/cIIr, common synthetic component nibten-11 common synthetic component 2/θ friend%) is blended with the additives shown in Table 1,
Using an inflation molding method (made by Flako Co., Ltd.! A θβ extruder equipped with an inflation die having a block slit with a diameter/θ0 angle and a slit gap/mm), the side fat temperature was λθθ℃, and the screw rotation speed was 60 r, p. ,m,
, extrusion@2/kg/hr0, blow-up ratio/,
! A cooling ring was installed at a position directly below the die at a pressure of 20 degrees Celsius to allow cooling water (20 degrees Celsius) to flow down along the outside of the cylindrical film, allowing rapid cooling at 3θm/min.
A film having a thickness of Zθμ was obtained.

得られたフィルムの透明性及び開口性を評価し第2表に
示した。
The transparency and openness of the obtained film were evaluated and shown in Table 2.

第2表 注二配合量は全てN社九である。Table 2 Note 2 All compounding amounts are from N Company 9.

実施例と〜/θ、比較例−t〜6 線状低密度ポリエチレンに替え、低密度ポリエチレン(
三菱化成工業■製、ツバチック−L−F /3/、メル
トインデツクヌ(/り0℃):/、31710分、密度
二〇、り2グ)を用いたほかは実施例/〜グと同様にフ
ィルムを得た。
Example and ~/θ, Comparative Example-t~6 Instead of linear low density polyethylene, low density polyethylene (
Examples/~g except that Mitsubishi Chemical Corporation ■, Tsubachik-L-F /3/, Melt Index (/0℃): /, 31710 minutes, density 20, 2g) were used. A film was obtained in the same manner.

得られたフィルムの透明性及び開口性を評価し、第3表
に示した。
The transparency and openness of the obtained film were evaluated and shown in Table 3.

第3表 :/韮二l!!l乙、・1コ゛童1モろ≧7更14%7
・・ある。
Table 3: / Nijil! ! l Otsu, 1 child 1 moro ≧ 7 more 14% 7
··be.

Claims (5)

【特許請求の範囲】[Claims] (1)  ポリオレフィン樹脂中に微粉状シリカをO8
OS〜/重量%、微粉状長石をO1θ!〜/M量%、脂
肪族カルボン酸アミドをθ、θ/〜0−jNfM−%配
合させて力るポリオレフィン組成物。
(1) Finely powdered silica is added to polyolefin resin at O8
OS~/wt%, fine powdered feldspar O1θ! A polyolefin composition containing ~/M amount % and aliphatic carboxylic acid amide in θ, θ/~0-jNfM-%.
(2)  ポリオレフィン樹脂か低密度ポリエチレンで
ある特許請求の範囲第1項に記載の組成物。
(2) The composition according to claim 1, which is a polyolefin resin or low density polyethylene.
(3)  ポリオレフィン樹脂か線状低密度ポリエチレ
ンである特許請求の範囲第1項に?il′載の組、放物
(3) In claim 1, which is polyolefin resin or linear low density polyethylene? The set il' is a parabola.
(4)  シリカが平均粒径/〜/θμのものである特
許請求の範囲第1項乃至第3項のいずれ力・に記載の組
成物。
(4) The composition according to any one of claims 1 to 3, wherein the silica has an average particle size of /~/θμ.
(5)長石が平均粒径/〜/θμのものである特許請求
の範囲第7項乃至第7項のいずれかに記載の組成物。
(5) The composition according to any one of claims 7 to 7, wherein the feldspar has an average particle size of /~/θμ.
JP20730482A 1982-11-26 1982-11-26 Polyolefin composition Granted JPS5998147A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20730482A JPS5998147A (en) 1982-11-26 1982-11-26 Polyolefin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20730482A JPS5998147A (en) 1982-11-26 1982-11-26 Polyolefin composition

Publications (2)

Publication Number Publication Date
JPS5998147A true JPS5998147A (en) 1984-06-06
JPH0149302B2 JPH0149302B2 (en) 1989-10-24

Family

ID=16537554

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20730482A Granted JPS5998147A (en) 1982-11-26 1982-11-26 Polyolefin composition

Country Status (1)

Country Link
JP (1) JPS5998147A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59210961A (en) * 1983-05-16 1984-11-29 Nippon Petrochem Co Ltd Resin composition for forming film having blocking resistance
JPS61241107A (en) * 1983-10-14 1986-10-27 グレイス・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング Bonding antitack agent and lubricant concentrate
US6029541A (en) * 1994-03-27 2000-02-29 Dr. Schrick Gmbh Reciprocating machine with neutralization of free inertial forces
EP1164162A1 (en) * 2000-06-13 2001-12-19 Wolff Walsrode Aktiengesellschaft Thermoplastic elastomer mixture with an improved processability in extrusion
JP2008111507A (en) * 2006-10-31 2008-05-15 Psc Kk Vibration eliminating device
CN113549262A (en) * 2020-04-26 2021-10-26 合肥杰事杰新材料股份有限公司 Antibacterial polypropylene material and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5743835A (en) * 1980-08-29 1982-03-12 Mitsubishi Chem Ind Ltd Manufacture of polyethylene film

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5743835A (en) * 1980-08-29 1982-03-12 Mitsubishi Chem Ind Ltd Manufacture of polyethylene film

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59210961A (en) * 1983-05-16 1984-11-29 Nippon Petrochem Co Ltd Resin composition for forming film having blocking resistance
JPH0463097B2 (en) * 1983-05-16 1992-10-08 Nippon Petrochemicals Co Ltd
JPS61241107A (en) * 1983-10-14 1986-10-27 グレイス・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング Bonding antitack agent and lubricant concentrate
US6029541A (en) * 1994-03-27 2000-02-29 Dr. Schrick Gmbh Reciprocating machine with neutralization of free inertial forces
EP1164162A1 (en) * 2000-06-13 2001-12-19 Wolff Walsrode Aktiengesellschaft Thermoplastic elastomer mixture with an improved processability in extrusion
JP2008111507A (en) * 2006-10-31 2008-05-15 Psc Kk Vibration eliminating device
CN113549262A (en) * 2020-04-26 2021-10-26 合肥杰事杰新材料股份有限公司 Antibacterial polypropylene material and preparation method thereof
CN113549262B (en) * 2020-04-26 2023-05-09 合肥杰事杰新材料股份有限公司 Antibacterial polypropylene material and preparation method thereof

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