JPH069850B2 - Method for forming polypropylene resin film - Google Patents

Method for forming polypropylene resin film

Info

Publication number
JPH069850B2
JPH069850B2 JP63041602A JP4160288A JPH069850B2 JP H069850 B2 JPH069850 B2 JP H069850B2 JP 63041602 A JP63041602 A JP 63041602A JP 4160288 A JP4160288 A JP 4160288A JP H069850 B2 JPH069850 B2 JP H069850B2
Authority
JP
Japan
Prior art keywords
film
cooling
sheet
polypropylene
water
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.)
Expired - Lifetime
Application number
JP63041602A
Other languages
Japanese (ja)
Other versions
JPH01214422A (en
Inventor
淳也 佐藤
征次 村上
喜久治 佐々木
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 JP63041602A priority Critical patent/JPH069850B2/en
Publication of JPH01214422A publication Critical patent/JPH01214422A/en
Publication of JPH069850B2 publication Critical patent/JPH069850B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
    • B29C48/9135Cooling of flat articles, e.g. using specially adapted supporting means
    • B29C48/915Cooling of flat articles, e.g. using specially adapted supporting means with means for improving the adhesion to the supporting means
    • B29C48/917Cooling of flat articles, e.g. using specially adapted supporting means with means for improving the adhesion to the supporting means by applying pressurised gas to the surface of the flat article
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
    • B29C48/9135Cooling of flat articles, e.g. using specially adapted supporting means
    • B29C48/914Cooling of flat articles, e.g. using specially adapted supporting means cooling drums

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)

Description

【発明の詳細な説明】 本発明は、ポリプロピレン系樹脂の製膜方法に関し、詳
しくは透明性、表裏面の均一性、すべり性、延伸性等の
優れたポリプロピレンフィルム等のシート状物が得られ
るポリプロピレン系樹脂の製膜方法に関するものであ
る。
The present invention relates to a method for forming a polypropylene resin, and more specifically, a sheet-like material such as a polypropylene film excellent in transparency, uniformity of front and back surfaces, slipperiness, and stretchability can be obtained. The present invention relates to a method for forming a polypropylene resin film.

〔従来の技術〕[Conventional technology]

従来、ポリプロピレン樹脂を溶融してT型ダイ法で押出
したシート物を冷却成型する方法としては、冷却ドラム
に該シート状物を接触させ、シート状物接地点に空気を
吹付け強制密着によるドラムからの冷却と空冷を狙った
エアーナイフ法や、ロールで冷却ドラムに密着させ冷却
成型するロール法などがある。また、インフレーシヨン
法でも、溶融状態のチューブに空気を吹付ける冷却法
や、水をリング状に流し、チューブ外周に接触させる水
冷法などが知られている。
Conventionally, as a method for cooling and molding a sheet material obtained by melting polypropylene resin and extruding it by a T-type die method, the sheet material is brought into contact with a cooling drum, and air is blown to a grounding point of the sheet material to forcibly adhere to the drum. There is an air knife method aimed at cooling from the air and air cooling, and a roll method in which a roll is brought into close contact with a cooling drum to perform cooling molding. Also known as the inflation method is a cooling method in which air is blown onto a molten tube, or a water cooling method in which water is caused to flow in a ring shape and is brought into contact with the outer circumference of the tube.

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

しかしながら、T型ダイ法によるエアーナイフ法やロー
ル法では、冷却ドラムからの冷却速度と空気吹き付け側
およびロール側からの冷却速度とに差があり、製膜され
たポリプロピレンフィルム表裏における高分子の結晶化
が異なつてくる。これはポリプロピレンフィルム厚みが
厚くなったり、製膜スピードが上がったりする程顕著に
なる。
However, in the air knife method and the roll method by the T-type die method, there is a difference between the cooling speed from the cooling drum and the cooling speed from the air blowing side and the roll side, and the polymer crystals on the front and back of the formed polypropylene film are different. There are different things. This becomes more prominent as the thickness of the polypropylene film increases and the film forming speed increases.

ポリプロピレンフィルム表裏の結晶化が異なった場合、
当然のことながら、結晶サイズや結晶化度が変り、その
後の延伸過程における球晶変形量や変形度合がフィルム
表裏で違ってくる。このため、フィルム表裏の表面形態
が違ったり、カールを起こしたりする原因となる。ま
た、透明性が悪化したボイドの多いフィルムとなったり
する。
If the crystallization of the front and back of the polypropylene film is different,
As a matter of course, the crystal size and the crystallinity change, and the spherulite deformation amount and the deformation degree in the subsequent stretching process are different between the front and back of the film. For this reason, the surface morphology of the front and back of the film may be different, or curling may occur. In addition, the film may have many voids with poor transparency.

このため、特開昭59−49937号公報で示されるよ
うな、水溶性又は水分散液で多数の泡抹をつくり、溶融
状態のプラスチックに泡抹を接触せしめることによって
冷却する方法が考え出されている。しかし、この方法で
は、フィルム品質として重要なフィルム厚みを均一化す
る手段がなく、例えばT型ダイ法における冷却成型で
は、ダイスから冷却ドラムまでの距離が長いため、この
間に起るシート状物の振動、シート状物の自重による垂
れ下がりが、得られるポリプロピレンフィルムの厚みム
ラ悪化原因となる。更にインフレーシヨン法において
も、チューブ外面の冷却は速いが内面からの冷却はでき
ておらず、フィルム内外面の結晶化が異なる。
For this reason, a method has been devised, as disclosed in JP-A-59-49937, in which a large number of foam particles are made from a water-soluble or water-dispersed liquid and the foam particles are brought into contact with molten plastic to cool the plastic particles. ing. However, in this method, there is no means for uniformizing the film thickness, which is important for film quality. For example, in cooling molding in the T-type die method, the distance from the die to the cooling drum is long, so that the sheet-like material that occurs during this period. Vibration and sagging of the sheet-like material due to its own weight cause deterioration of the thickness unevenness of the obtained polypropylene film. Further, also in the inflation method, the outer surface of the tube is cooled rapidly, but the inner surface is not cooled, and the crystallization of the inner and outer surfaces of the film is different.

また、実開昭53−134262号公報には、フィルム
面のフローマークやボイルマークのない外観上均一なフ
ィルムを得るために、溶融押出し後のフィルムにエアー
混合噴霧ノズルで水滴を付与する装置が示されている。
Further, Japanese Utility Model Application Laid-Open No. 53-134262 discloses a device for imparting water droplets to a film after melt extrusion with an air mixing spray nozzle in order to obtain a film having a uniform appearance without flow marks or boil marks on the film surface. It is shown.

この装置で開示している手段によれば、フィルム面のフ
ローマークやボイルマークは解消されるが、透明性、均
一性、延伸性などにおいてまだ満足できるものは得られ
ないという問題点が残る。
According to the means disclosed in this apparatus, the flow mark and the boil mark on the film surface are eliminated, but there is a problem that transparency, uniformity, stretchability and the like cannot be obtained yet.

またポリプロピレン系樹脂の場合、溶融押出後冷却する
過程で結晶化が進行するが、冷却効率が悪いと徐冷とな
り、結晶がより大きく成長した透明性の悪いフィルムに
なるという問題が生ずる。
Further, in the case of a polypropylene resin, crystallization progresses in the process of cooling after melt extrusion, but if the cooling efficiency is poor, the film is gradually cooled, resulting in a problem that the film becomes larger and the film has poor transparency.

一方、ポリプロピレン系延伸フィルムにおいては、特開
昭60−88049号公報に示されているごとく、延伸
フィルムにすべり性、透明性、抗ブロッキング性を付与
する目的で無機粒子および造核剤等を添加することが行
われる。しかし、無機粒子と造核剤のみでは無機粒子の
添加による透過光の散乱により透明性が悪化するという
欠点がある。
On the other hand, in a polypropylene-based stretched film, as disclosed in JP-A-60-88049, inorganic particles and a nucleating agent are added for the purpose of imparting slipperiness, transparency and anti-blocking property to the stretched film. Is done. However, there is a drawback in that the transparency is deteriorated due to the scattering of transmitted light due to the addition of the inorganic particles when only the inorganic particles and the nucleating agent are used.

さらに、特公昭56−53489号には、造核剤を添加
したポリプロピレンフィルムを鏡面仕上げされた冷却ロ
ールで冷却することにより、透明性と平滑性を付与する
ことが開示されている。しかし、この方法でも冷却効率
が悪いため、透明性の面でまだ不十分である。
Further, Japanese Patent Publication No. 56-53489 discloses that a polypropylene film containing a nucleating agent is cooled with a mirror-finished cooling roll to impart transparency and smoothness. However, this method is still inadequate in terms of transparency because the cooling efficiency is poor.

従って本発明の目的は、上記欠点を解消し、透明性、す
べり性、延伸性に優れ、表裏面が均一でカールのないポ
リプロピレン系フィルムが得られるポリプロピレン系樹
脂の製膜方法を提供せんとするものである。
Therefore, an object of the present invention is to provide a method for forming a polypropylene resin, which solves the above-mentioned drawbacks, is excellent in transparency, slipperiness, and stretchability, and obtains a polypropylene film having uniform front and back surfaces and no curl. It is a thing.

〔課題を解決するための手段〕[Means for Solving the Problems]

本発明は、上記目的を達成させるため、次の構成を有す
る。すなわち、ポリプロピレン系樹脂をダイより溶融押
出ししシート状物とし、該シート状物を冷却ドラムに接
触させて冷却固化してポリプロピレン系樹脂を製膜する
方法において、該ポリプロピレン系樹脂に造核剤および
平均粒径0.1〜10μmの無機粒子を0.05〜1.
0重量%添加し、前記シート状物が鏡面仕上げされた冷
却ドラムに接触した後、前記シート状物の該冷却ドラム
に接触している面とは反対側の表面に、水を微粒子の霧
状にして吹きつけることを特徴とするポリプロピレン系
樹脂の製膜方法である。
The present invention has the following configuration in order to achieve the above object. That is, a polypropylene resin is melt-extruded from a die to form a sheet, and the sheet is brought into contact with a cooling drum to be cooled and solidified to form a polypropylene resin. Inorganic particles having an average particle diameter of 0.1 to 10 μm are added in an amount of 0.05 to 1.
After the addition of 0% by weight, the sheet-like material comes into contact with a mirror-finished cooling drum, and then water is sprayed on the surface of the sheet-like material opposite to the surface in contact with the cooling drum to atomize fine particles. It is a method for forming a polypropylene resin film, which comprises spraying.

本発明でいうポリプロピレン系樹脂とは、ポリプロピレ
ン成分が80重量%以上を含有する樹脂をいう。
The polypropylene-based resin in the present invention means a resin containing a polypropylene component in an amount of 80% by weight or more.

本発明においては、ポリプロピレン系樹脂に樹脂の結晶
造核効果を持つ造核剤を少量添加する必要があり、それ
によって後述するごとく、ポリプロピレンフィルムの透
明性が著しく向上するようになる。なお、造核剤の種類
としては、ポリプロピレン系樹脂の結晶造核効果を持つ
安息香酸アルミニウム、1,3,2,4−ジベンジリジ
ン−D−ソルビトール等であるが、これに限定されな
い。その添加量としては0.01〜1.0重量%程度が
好ましい。
In the present invention, it is necessary to add a small amount of a nucleating agent having a crystal nucleation effect of the resin to the polypropylene-based resin, which will significantly improve the transparency of the polypropylene film as described later. The type of nucleating agent is aluminum benzoate, which has the crystal nucleating effect of polypropylene resin, 1,3,2,4-dibenzilidine-D-sorbitol, but is not limited thereto. The amount added is preferably about 0.01 to 1.0% by weight.

また、本発明でいう無機粒子とは、シリカ、サイロイ
ド、カオリナイト、ゼオライト、酸化チタン、炭酸カル
シウム等である。そしてポリプロピレンフィルムのすべ
り性および透明性の両面から、この無機粒子の平均粒径
を0.1〜10μmの範囲とし、添加量を0.05〜
1.0重量%の範囲とすることが必要である。
Further, the inorganic particles referred to in the present invention are silica, siloid, kaolinite, zeolite, titanium oxide, calcium carbonate and the like. From the viewpoints of slipperiness and transparency of the polypropylene film, the average particle diameter of the inorganic particles is set to 0.1 to 10 μm, and the addition amount is set to 0.05 to
It is necessary to set it in the range of 1.0% by weight.

冷却ドラムはポリプロピレンフィルムの優れた透明性お
よび均一性を付与するために鏡面仕上げされている必要
がある。その材質としてはドラム表面にハードクロム
(HCr)を巻いたものや、セラミック、シリコーンゴ
ム等を加工しドラム表面としたものが使用できる。
The cooling drum must be mirror-finished to give the polypropylene film excellent transparency and uniformity. As the material, a material in which hard chrome (HCr) is wound on the drum surface or a material obtained by processing ceramic, silicone rubber or the like to form the drum surface can be used.

ドラム表面を冷却する方法としては、ドラム内部に常水
やチルド水または温水を通して内部から冷却するのが良
く、本発明における冷却ドラムの表面温度は、5℃から
80℃の範囲が好ましい。冷却ドラムの表面温度が5℃
未満になると、外気との温度差から露滴が発生し、フィ
ルム表面に欠点として残る。また、冷却ドラムの表面温
度が80℃を越えた場合、冷却効果が劣りボイドの多い
透明性の悪化したフィルムとなる。
As a method for cooling the surface of the drum, it is preferable to cool the inside of the drum by passing ordinary water, chilled water or warm water, and the surface temperature of the cooling drum in the present invention is preferably in the range of 5 ° C to 80 ° C. Surface temperature of the cooling drum is 5 ℃
When it is less than the above, dew drops are generated due to the temperature difference from the outside air, and remain as a defect on the film surface. Further, when the surface temperature of the cooling drum exceeds 80 ° C., the film is poor in cooling effect and has many voids, resulting in poor transparency.

本発明においては、特に限定するものではないが、ダイ
より溶融押出しされたシート状物を、エアーナイフ法又
はロール法でドラムに密着させることができる。
In the present invention, although not particularly limited, the sheet-like material melt-extruded from the die can be adhered to the drum by an air knife method or a roll method.

この時ダイから冷却ドラムまでの距離は、成型上支障の
ない限り近づけた方が良く、シート状物の振動やバタツ
キをなくすとともに、結晶化時間を短くできる。
At this time, the distance from the die to the cooling drum should be close as long as there is no hindrance in molding, so that the vibration and fluttering of the sheet-like material can be eliminated and the crystallization time can be shortened.

また、エアーナイフ法のエアー風速やロール法のロール
温度は、成形上支障のない限り冷却側になるよう設定す
るのが良い。
In addition, the air velocity of the air knife method and the roll temperature of the roll method are preferably set on the cooling side as long as there is no hindrance in molding.

エアーナイフ法やロール法で、冷却ドラムに密着された
シート状物の非冷却ドラム面側に、水を微粒子の霧状に
して吹付ける。本発明に適用できる、水を微粒子の霧状
にする方法としては、例えば静電塗装機などに用いられ
る、空気霧化、静電霧化、空気併用静電霧化、液圧霧化
およびスプレーガン式、旋回気流式があり、更に、超音
波加湿器による霧化などがある。吹付ける水粒子の径は
特に限定しないが、100μm以下が好ましい。水粒径
が100μmを越えると液玉になり易く、フィルム表面
に欠点として残る。また、本発明の作用である蒸発潜熱
による冷却が成しがたいものとなる。すなわち、流水に
よる冷却では、熱量の移動は水の吸熱のみであるが、水
を蒸発させた場合、吸熱と蒸発潜熱による熱移動が起こ
る。これは、流水による冷却に比べ10倍以上の冷却効
果がある。それ故、水粒子は表面積が大きく蒸発し易い
よう、小さくとるのが好ましい。
By an air knife method or a roll method, water is atomized into fine particles and sprayed on the non-cooling drum surface side of the sheet-like material that is in close contact with the cooling drum. As a method for atomizing water into fine particles, which can be applied to the present invention, for example, used in an electrostatic coating machine, air atomization, electrostatic atomization, electrostatic atomization with air, hydraulic atomization and spraying. There are a gun type and a swirling airflow type, and further atomization by an ultrasonic humidifier. The diameter of water particles to be sprayed is not particularly limited, but is preferably 100 μm or less. If the water particle size exceeds 100 μm, liquid droplets tend to be formed and remain as a defect on the film surface. Further, the cooling by the latent heat of vaporization, which is the function of the present invention, is difficult to achieve. That is, in cooling with running water, the amount of heat is transferred only by absorbing heat of water, but when water is evaporated, heat transfer due to heat absorption and latent heat of evaporation occurs. This has a cooling effect 10 times or more compared with the cooling by running water. Therefore, it is preferable to make the water particles small so that they have a large surface area and are easily evaporated.

なお、本発明の方法では結晶造核剤を添加するひつよう
があるが、それによりポリプロピレン系樹脂の結晶化す
る温度範囲が高く、また結晶化が早くなる。従って、冷
却ドラムに密着されたシート状物の非冷却ドラム面側に
水を微粒子の霧状にして吹付け、冷却を強化することに
より、溶融押出し後の冷却過程で生成する結晶の核がよ
り多く、また結晶化が早くなるため結晶がより微細にな
り透明性が著しく向上するようになる。また、同時に表
裏の冷却結晶化の差が小さくなってカールの小さいフィ
ルムとなる。
In the method of the present invention, it is necessary to add a crystal nucleating agent, but the temperature range in which the polypropylene resin is crystallized is high and the crystallization is fast. Therefore, by spraying water in the form of fine particles onto the non-cooling drum surface side of the sheet-like material adhered to the cooling drum to intensify the cooling, the nuclei of crystals generated in the cooling process after melt extrusion are further improved. In many cases, the crystallization becomes faster, so that the crystals become finer and the transparency is significantly improved. At the same time, the difference in cooling and crystallization between the front and the back becomes small, resulting in a film with small curl.

また、吹付ける位置は、該シート状物が冷却ドラムに接
地した後であるが、接地点からできるだけ近くが、結晶
化抑制およびフィルム表裏の結晶化差を小さくできて良
い。
The sheet is sprayed at a position after the sheet is grounded on the cooling drum, but as close as possible to the grounding point, crystallization can be suppressed and the difference in crystallization between the front and back of the film can be reduced.

本発明における吹付け方法は、霧化発生装置から、ホー
ス管等継手を介して、スリツト型ノズル幅方向均一噴霧
が良い。
The spraying method according to the present invention is preferably a uniform spray in the width direction of the slit type nozzle from the atomization generator through a joint such as a hose pipe.

スリット型ノズルを使用した場合、吹付け角度θ(ノズ
ルの方向と重力方向の角度)は、45〜90゜の範囲内
にするのがよい。θをこの範囲外にすると、凝集した液
玉がシート状物上へ飛んだり、冷却効果が薄れたりす
る。例えば、θを105゜とすると、ノズルの先に凝集
した液玉が飛んで、その液玉がシート状物表面に付着
し、液玉の付着したところが製膜後のフィルムの表面欠
点となることがある。
When a slit type nozzle is used, the spraying angle θ (angle between the nozzle direction and the gravity direction) is preferably in the range of 45 to 90 °. If θ is out of this range, agglomerated liquid beads may fly onto the sheet-like material or the cooling effect may be weakened. For example, if θ is 105 °, the liquid droplets that have agglomerated at the tip of the nozzle will fly, and the liquid droplets will adhere to the surface of the sheet-like material, and the places where the liquid droplets adhere will be surface defects of the film after film formation. There is.

なお、本発明におけるシート状物には押出ラミネーショ
ンによって得られラミネートも含まれる。その場合もラ
ミネートが冷却ドラムに接した後、冷却ドラムに接して
いるラミネートの面とは反対側の表面に、水を微粒子の
霧状にして吹付ける。
The sheet material in the present invention includes a laminate obtained by extrusion lamination. Also in this case, after the laminate comes into contact with the cooling drum, water is sprayed in the form of fine particles onto the surface of the laminate opposite to the surface in contact with the cooling drum.

また、冷却ドラム速度、フィルム成型速度やフィルム厚
みの変更により、噴霧流速、噴霧流量を適宜選択するの
が良い。
Further, it is preferable to appropriately select the spray flow rate and the spray flow rate by changing the cooling drum speed, the film forming speed, and the film thickness.

〔実施例〕〔Example〕

以下、本発明の実施例を図面に基づいて説明する。但
し、本発明は以下の実施例に限定されるものではない。
Embodiments of the present invention will be described below with reference to the drawings. However, the present invention is not limited to the following examples.

実施例1 第1図に、本発明の方法に使用する装置の一例を示す。
1は押出機、2は押出機のT型ダイ、3は鏡面仕上げさ
れたハードクロムを表面にもつ冷却ドラム、4はシート
状物を冷却ドラムに密着させるエアーナイフ、5は霧化
発生装置、6は貯水槽、7はスリット型ノズル、8は霧
化発生装置とスリツト型ノズルを継ぐホース管、9はポ
リプロピレン樹脂シート状物であり、矢印は重力方向を
示す。この図では、スリツト型ノズルの重力方向に対す
る角度θを80℃としている。
Example 1 FIG. 1 shows an example of an apparatus used in the method of the present invention.
DESCRIPTION OF SYMBOLS 1 is an extruder, 2 is a T-shaped die of the extruder, 3 is a cooling drum having a mirror-finished hard chrome on its surface, 4 is an air knife for adhering a sheet-like material to the cooling drum, 5 is an atomization generator, 6 is a water tank, 7 is a slit type nozzle, 8 is a hose pipe connecting the atomization generator and the slit type nozzle, 9 is a polypropylene resin sheet, and the arrow indicates the direction of gravity. In this figure, the angle θ of the slit type nozzle with respect to the direction of gravity is 80 ° C.

第1図の装置を用いて、以下のようにポリプロピレンを
製膜した。ポリプロピレン100重量部に無機粒子(シ
リカ、平均粒径3.5μm)0.5重量%および造核剤
として安息香酸アルミニウム0.1重量%を添加した樹
脂を、ホッパーより押出機1に投入し、溶融温度260
℃でT型ダイ2より冷却ドラム3上に押出した。この味
のシート状物9の厚みは1mmあった。
Using the apparatus shown in FIG. 1, polypropylene was formed into a film as follows. A resin obtained by adding 0.5% by weight of inorganic particles (silica, average particle diameter 3.5 μm) and 0.1% by weight of aluminum benzoate as a nucleating agent to 100 parts by weight of polypropylene was charged into the extruder 1 from a hopper, Melting temperature 260
It was extruded from the T-die 2 onto the cooling drum 3 at ℃. The thickness of this taste-like sheet material 9 was 1 mm.

冷却ドラム3上のシート状物4に、重力方向に対して8
0゜の角度で、スリット型ノズル7から水を粒子径約1
μmの霧状にして吹付け、冷却固化せしめた。
On the sheet-shaped material 4 on the cooling drum 3, 8
At an angle of 0 °, water from the slit type nozzle 7 has a particle size of about 1
It was made into a mist of μm and sprayed, and then cooled and solidified.

その後、延伸温度120℃で長手方向に5倍延伸し、次
いでこの一軸延伸フィルムを160℃に保温されたステ
ンタに導き横手方向に7倍に延伸した。
Then, it was stretched 5 times in the longitudinal direction at a stretching temperature of 120 ° C., and then this uniaxially stretched film was introduced into a stenter kept at 160 ° C. and stretched 7 times in the transverse direction.

延伸過程における製膜性は良好であり、フィルム表裏に
おいて結晶化の均一な表裏面形状の異ならない、しかも
ボイドの少ないフィルムが得られた。得られたフィルム
の視覚透明度を測定したところ、NASが3.8で、L
SIが1.8であり、透明性に優れていた。
The film-forming property in the stretching process was good, and a film with uniform crystallization on the front and back sides of the film, with different front and back surface shapes and less voids was obtained. When the visual transparency of the obtained film was measured, the NAS was 3.8, and the L
SI was 1.8 and it was excellent in transparency.

ここで、視覚透明度とは、曇り度合の尺度である。従来
の曇価測定(JIS K6714等)に比べ、より人間
の目に近い受光角で測定する。人間の目の入射角は明所
で0.7゜、暗所で1.4゜であり、ここで用いられて
いるNAS(狭角透過光物性値)とは、−0.4゜〜
0.4゜の透過光、LSI(狭角拡散透過値)とは、−
1.2゜〜−0.4゜および1.2゜〜0.4゜の散乱
光を測定しており、その測定は、東洋精機製作所製の視
覚透明度試験機を用いて行なった。
Here, the visual transparency is a measure of the degree of haze. Compared with the conventional cloudiness value measurement (JIS K6714 etc.), the light receiving angle is closer to the human eye. The incident angle of the human eye is 0.7 ° in a bright place and 1.4 ° in a dark place, and the NAS (narrow-angle transmitted light property value) used here is -0.4 ° to
0.4 ° transmitted light, LSI (narrow angle diffuse transmission value)-
The scattered light of 1.2 ° to −0.4 ° and 1.2 ° to 0.4 ° was measured, and the measurement was performed using a visual transparency tester manufactured by Toyo Seiki Seisakusho.

比較例1 実施例1において、水を霧状にして吹付けることをしな
い点および造核剤を添加しない点以外は実施例1と同様
に行なった。
Comparative Example 1 The procedure of Example 1 was repeated, except that water was not atomized and sprayed, and that no nucleating agent was added.

得られたフィルムの視覚透明度を測定したところ、NA
Sが6.4でLSIが6.7であり、実施例1のフィル
ムに比べ、透明性がかなり劣っていた。
The visual transparency of the obtained film was measured and found to be NA
The S was 6.4 and the LSI was 6.7, and the transparency was considerably inferior to the film of Example 1.

比較例2 実施例1において、水を霧状にして吹付けることをしな
い点以外は、実施例1と同様に行った。すなわち、造核
剤として安息香酸アルミニウム0.1重量%を添加した
樹脂から溶融押出、冷却成形、二軸延伸し、フィルムを
得た。得られたフィルムは、NASが4.5で、LSI
が3.1であり、比較例1と比較すると透明性は改良さ
れたものの実施例1より劣り、カールの大きいものであ
った。
Comparative Example 2 The procedure of Example 1 was repeated, except that the water was not atomized and sprayed. That is, a film was obtained by melt-extruding, cooling-molding and biaxially stretching a resin containing 0.1% by weight of aluminum benzoate as a nucleating agent. The resulting film has a NAS of 4.5 and is an LSI
Is 3.1, which is inferior to that in Example 1 and has a large curl as compared with Comparative Example 1 although the transparency is improved.

〔発明の効果〕〔The invention's effect〕

本発明は、次のような効果を奏する。 The present invention has the following effects.

(1)ポリプロピレンフィルムの表裏において、結晶化
の均一な表裏面形状の異ならないフィルムが得られる。
(1) On the front and back of a polypropylene film, a film having uniform front and back surfaces with uniform crystallization can be obtained.

(2)冷却効果が高いため、透明性の良いポリプロピレ
ンフィルムが得られる。
(2) Since the cooling effect is high, a polypropylene film having good transparency can be obtained.

(3)ポリプロピレンフィルム表裏の結晶化が均一なた
め、二軸延伸を行ってもフィルム表裏の配向が異なら
ず、カールが起こらない、延伸性に優れたフィルムとな
る。
(3) Since the front and back surfaces of the polypropylene film are uniformly crystallized, the orientation of the front and back surfaces of the film does not change even when biaxially stretched, and a curl-free film having excellent stretchability is obtained.

【図面の簡単な説明】[Brief description of drawings]

第1図は、本発明を適用した製膜装置の一実施態様を示
す。 1……押出機、2……T型ダイ、3……冷却ドラム、4
……エアーナイフ、5……霧化発生装置、6……貯水
槽、7……スリット型ノズル、8……ホース管、9……
ポリプロピレン樹脂シート状物
FIG. 1 shows an embodiment of a film forming apparatus to which the present invention is applied. 1 ... Extruder, 2 ... T-die, 3 ... Cooling drum, 4
…… Air knife, 5 …… Atomization generator, 6 …… Water tank, 7 …… Slit nozzle, 8 …… Hose pipe, 9 ……
Polypropylene resin sheet

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】ポリプロピレン系樹脂をダイより溶融押出
ししシート状物とし、該シート状物を冷却ドラムに接触
させて冷却固化してポリプロピレン系樹脂を製膜する方
法において、該ポリプロピレン系樹脂に造核剤および平
均粒径0.1〜10μmの無機粒子を0.05〜1.0
重量%添加し、前記シート状物が鏡面仕上げされた冷却
ドラムに接触した後、前記シート状物の該冷却ドラムに
接触している面とは反対側の表面に、水を微粒子の霧状
にして吹きつけることを特徴とするポリプロピレン系樹
脂の製膜方法。
A polypropylene resin is melt extruded from a die to form a sheet, and the sheet is brought into contact with a cooling drum to solidify by cooling to form a polypropylene resin into a film. Nucleating agent and inorganic particles having an average particle size of 0.1 to 10 μm are used in an amount of 0.05 to 1.0.
% By weight, and the sheet-like material comes into contact with a mirror-finished cooling drum, and then water is atomized into fine particles on the surface of the sheet-like material opposite to the surface in contact with the cooling drum. A method for forming a polypropylene-based resin film, which comprises spraying.
JP63041602A 1988-02-23 1988-02-23 Method for forming polypropylene resin film Expired - Lifetime JPH069850B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63041602A JPH069850B2 (en) 1988-02-23 1988-02-23 Method for forming polypropylene resin film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63041602A JPH069850B2 (en) 1988-02-23 1988-02-23 Method for forming polypropylene resin film

Publications (2)

Publication Number Publication Date
JPH01214422A JPH01214422A (en) 1989-08-28
JPH069850B2 true JPH069850B2 (en) 1994-02-09

Family

ID=12612927

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63041602A Expired - Lifetime JPH069850B2 (en) 1988-02-23 1988-02-23 Method for forming polypropylene resin film

Country Status (1)

Country Link
JP (1) JPH069850B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0414426A (en) * 1990-05-08 1992-01-20 Mitsubishi Heavy Ind Ltd Apparatus for molding film or sheet
JP4538123B2 (en) * 1999-11-30 2010-09-08 日本ポリプロ株式会社 Propylene polymer sheet thermoformed product

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5353474U (en) * 1976-10-07 1978-05-08
JPS6020710B2 (en) * 1979-10-09 1985-05-23 原子燃料工業株式会社 Support grid for nuclear fuel assembly
JPS6088049A (en) * 1983-10-20 1985-05-17 Toray Ind Inc Biaxially oriented polypropylene film

Also Published As

Publication number Publication date
JPH01214422A (en) 1989-08-28

Similar Documents

Publication Publication Date Title
CN101312818B (en) Thermoplastic resin film and its manufacturing process
CN101312816A (en) Method for manufacturing cellulose resin film
CN101405126A (en) Thermoplastic resin film and method for producing the same
JP2007185898A (en) Biaxially oriented polyester film and its manufacturing process
WO2005090073A1 (en) Layered polypropylene film, process for producing the same, and package comprising the same
JPH069850B2 (en) Method for forming polypropylene resin film
JP2005297544A (en) Polypropylene type laminated film and package using it
JP2011502064A5 (en)
CN101262995A (en) Cellulose-based resin film and production method of the same
JPS6316256B2 (en)
JPS6140539B2 (en)
JPH11320671A (en) Manufacture of and device for stretched film
JPS59150726A (en) Manufacture of thermoplastic resin sheet or film
KR100215480B1 (en) Method of manufacturing propylene-based polymer film
GB894147A (en) Extrusion process and apparatus
KR100193686B1 (en) Propylene Resin Sheet and Manufacturing Method Thereof
JPH0119332B2 (en)
KR20000073060A (en) The Processing Method for Thermoplastic Resin Sheet Manufacture
JPH0939088A (en) Manufacture of polystyrene film
JPH07266417A (en) Production of transparent laminated resin film having non-fogging properties
JPS61219621A (en) Manufacture of thermoplastic resin film
JPS5850173B2 (en) Manufacturing method of polyester film
JPH043897B2 (en)
KR19980017430A (en) Propylene Resin Sheet and Manufacturing Method Thereof
JPS6172509A (en) Forming process of resin sheet