JPS6325016A - Manufacture of thermoplastic resin film - Google Patents
Manufacture of thermoplastic resin filmInfo
- Publication number
- JPS6325016A JPS6325016A JP61167883A JP16788386A JPS6325016A JP S6325016 A JPS6325016 A JP S6325016A JP 61167883 A JP61167883 A JP 61167883A JP 16788386 A JP16788386 A JP 16788386A JP S6325016 A JPS6325016 A JP S6325016A
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- cooling roll
- film
- thermoplastic resin
- resin film
- 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.)
- Pending
Links
- 229920005992 thermoplastic resin Polymers 0.000 title claims description 33
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 238000001816 cooling Methods 0.000 claims abstract description 62
- 239000007788 liquid Substances 0.000 claims abstract description 40
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 abstract description 23
- 229920005989 resin Polymers 0.000 abstract description 20
- 239000011347 resin Substances 0.000 abstract description 20
- 238000000465 moulding Methods 0.000 abstract description 8
- 238000009835 boiling Methods 0.000 abstract description 7
- 239000010408 film Substances 0.000 description 61
- 230000000052 comparative effect Effects 0.000 description 7
- 230000007547 defect Effects 0.000 description 7
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 230000003068 static effect Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 230000037303 wrinkles Effects 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- ZAOJWJAARUYTMA-UHFFFAOYSA-N 4-chloro-2-(5-chloro-2-hydroxy-3-nitrophenyl)sulfanyl-6-nitrophenol Chemical compound C1=C(Cl)C=C([N+]([O-])=O)C(O)=C1SC1=CC(Cl)=CC([N+]([O-])=O)=C1O ZAOJWJAARUYTMA-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/9175—Cooling of flat articles, e.g. using specially adapted supporting means by interposing a fluid layer between the supporting means and the flat article
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion 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
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/914—Cooling 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)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は熱可塑性樹脂フィルム(本願明細書ではミート
もフィルムの類に入れるものとする)の製造方法に関し
、更に詳しくは溶融熱可塑性樹脂をダイから移動冷却ロ
ール面上に押出し熱可塑性樹脂フィルムを製造する際、
該フィルムと移動冷却ロール間の密着性を向上せしめ、
表面品質の極めてすぐれた熱可塑性樹脂フィルムを高速
で製造する方法に関するものである。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a method for producing a thermoplastic resin film (in the present specification, meat is also included in the category of film), and more specifically relates to a method for producing a thermoplastic resin film (in this specification, meat is also included in the category of film). When producing the extruded thermoplastic film from the die onto the cooling roll surface,
Improving the adhesion between the film and the moving cooling roll,
The present invention relates to a method for producing thermoplastic resin films with extremely excellent surface quality at high speed.
一般に熱可塑性樹脂フィルムは、押出ダイよシ熱可塑性
樹脂が溶融状態で押出され、これが強制的に冷却されて
いる移動冷却ロール上に流延せしめられて冷却固化し、
しかるのちに該ロールから剥ぎとられることによって製
造される。Generally, thermoplastic resin films are produced by extruding a molten thermoplastic resin through an extrusion die, casting it onto a moving cooling roll that is forcibly cooled, and solidifying it by cooling.
It is then manufactured by peeling off the roll.
しかしながら、かかる方法においては種々のトラブルが
ちυ、所望の品質を有する樹脂フィルムを得ることは事
実上不可能であった。However, such a method is prone to various troubles, and it has been virtually impossible to obtain a resin film having the desired quality.
すなわち、第一に溶融状態の熱可塑性樹脂が移動冷却ロ
ール入面でスベリな生じ、冷却固化された樹脂フィルム
表面にシワやたるみが生じ易く、第二にこのようなスベ
リが生じない場合にも移動冷却ロール表面での急冷によ
り、フィルム巾が減少して巾の不規則な樹脂フィルムが
生成し易く、第三に溶融熱可塑性樹脂と移動冷却ロール
との間の空気の不規則な巻き込みにより、樹脂フィルム
に凹凸や冷却ムラが生じ易く、第四に溶融熱可塑性樹脂
が移動冷却ロールに接触する位置が安定せず不規則に変
化するため、樹脂フィルムに厚みムラや冷却斑等が発生
し易い等の欠陥があった。しかもこれらの現象は生産量
の増大に伴う移動冷却ロールの移動速度の上昇に伴い一
層顕著化していた。That is, firstly, the thermoplastic resin in the molten state tends to slip on the entrance surface of the moving cooling roll, causing wrinkles and sagging on the surface of the cooled and solidified resin film, and secondly, even when such slipping does not occur, Due to rapid cooling on the surface of the moving cooling roll, the film width tends to decrease and a resin film with irregular width is likely to be produced. Thirdly, due to the irregular entrainment of air between the molten thermoplastic resin and the moving cooling roll, The resin film tends to have unevenness and cooling unevenness.Fourth, the position where the molten thermoplastic resin contacts the moving cooling roll is unstable and changes irregularly, so the resin film tends to have uneven thickness and cooling spots. There were other defects. In addition, these phenomena have become more pronounced as the moving speed of the moving cooling roll increases as the production volume increases.
これらの欠陥はいずれも溶融熱可塑性樹脂と移動冷却ロ
ールとの間の密着性の不充分さに起因するものと考えら
れ、この密着性を向上せしめる試みが従来より種々行な
われてきた。All of these defects are thought to be caused by insufficient adhesion between the molten thermoplastic resin and the moving cooling roll, and various attempts have been made to improve this adhesion.
まず、第一に押出された溶融熱可塑性樹脂光面に空気を
吹付けたシ、あるいは圧着ドラムで機械的に押しつける
方法が知られている。しかしながら、前者にあっては気
流の乱れ、流体圧の変動等によシ樹脂フィルムの表面性
が限定されてし−まう等の欠陥があった。First, a method is known in which the optical surface of the extruded molten thermoplastic resin is mechanically pressed by blowing air or by using a pressure drum. However, the former method has the disadvantage that the surface properties of the resin film are limited due to turbulence in airflow, fluctuations in fluid pressure, etc.
第二に溶融熱可塑性樹脂側の表面もしくはその反対面、
または絶縁被覆した移動冷却ロール面上に静電荷を析出
せしめ、同時に移動冷却ロールを接地させ、溶融熱可塑
性樹脂と移動冷却ロールとの間に異種の静電荷による電
気的引力な生ぜしめて、溶融熱可塑性樹脂を移動冷却ロ
ールに密着せしめようという方法が知られている(たと
えば特公昭37−6142号、特公昭48−3535号
、特公昭48−14786号、特公昭48−14785
号、特公昭48−14786号、特公昭48−2931
1号公報等)。Second, the surface on the molten thermoplastic resin side or the opposite surface,
Alternatively, electrostatic charges are deposited on the surface of the moving cooling roll coated with insulation, and at the same time the moving cooling roll is grounded, and an electric attraction is generated between the molten thermoplastic resin and the moving cooling roll due to different types of static charges, and the melting heat is generated. A method of bringing a plastic resin into close contact with a moving cooling roll is known (for example, Japanese Patent Publication No. 37-6142, Japanese Patent Publication No. 3535-1982, Japanese Patent Publication No. 14786-1973, Japanese Patent Publication No. 14786-1985).
No., Special Publication No. 1978-14786, Special Publication No. 48-2931
Publication No. 1, etc.).
これらの方法にあっては前述した従来の欠陥の多くは解
消されるものの、静電荷の局部的な集中によシ溶融熱可
塑性樹脂に急激な力が加わり、急激な応力変化を受けて
樹脂フィルム面にシワや厚みムラが生じ易く、密着が強
力であるためにかえって移動冷却ロール表面の欠陥をそ
のまま樹脂フィルムに転写してしまったシ、また密着後
にも残存する静電荷のため塵埃が付着して局部的な斑を
つくり易く、更には生産量増大のために移動冷却ロール
の移動速度を増大したときには溶融熱可塑性樹脂が移動
冷却ロールと押出ダイとの間で膜振動する現象がみられ
、このため樹脂フィルムの巾の周期的変動や冷却斑を発
生し易い等の新たな欠陥が生じ、必ずしも満足し得る品
質の樹脂フィルムを得ることは出来なかった。Although these methods eliminate many of the conventional defects mentioned above, the local concentration of static charge applies a sudden force to the molten thermoplastic resin, causing the resin film to undergo a sudden change in stress. Wrinkles and thickness unevenness tend to occur on the surface, and because the adhesion is so strong, defects on the surface of the moving cooling roll are transferred directly to the resin film.Furthermore, the static charge that remains even after adhesion causes dust to adhere. Furthermore, when the moving speed of the moving cooling roll is increased to increase production, a phenomenon in which the molten thermoplastic resin vibrates between the moving cooling roll and the extrusion die is observed. As a result, new defects such as periodic fluctuations in the width of the resin film and the tendency to generate cooling spots occur, and it is not always possible to obtain a resin film of satisfactory quality.
第三に溶融熱可塑性樹脂と移動冷却ロールとの間に液体
を介在させる方法が知られている〇このうち英国特許第
1,312,519号明細書に開示された方法は、上述
した静電荷を用いる方法を併用しつつ、更に移動冷却ロ
ール表面に熱伝導性液体超極薄被膜を設け、この上に熱
可塑性樹脂を押出すことによって、これまで静電荷によ
る方法の抱えていた強力すぎる密着効果による移動冷却
ロールの表面欠陥の転写という欠陥を除去せんとするも
のである。Thirdly, a method is known in which a liquid is interposed between a molten thermoplastic resin and a moving cooling roll. Of these, the method disclosed in British Patent No. 1,312,519 is a method that eliminates the above-mentioned electrostatic charge. By using a method that uses a static charge in combination, and also applying an ultra-thin layer of thermally conductive liquid on the surface of a moving cooling roll and extruding a thermoplastic resin on top of this, we are able to overcome the excessively strong adhesion that conventional methods using static charges have had. This is intended to eliminate defects such as transfer of surface defects on the moving cooling roll due to the effect.
しかしながら、かかる方法においては、移動冷却ロール
上の熱伝導性液体超極薄被膜が移動冷却ロールを再使用
するとき(冷却ロールが1回転したとき)までに蒸発及
び熱可塑性樹脂の吸収によって移動冷却ロール表面から
消費つくされてしまうことか要求されるが、一般にこの
消費量は極めて少ないために被膜厚は極めて薄くする必
要がめる。この被膜厚は対象とする熱可塑性樹脂の種類
、移動冷却ロールの温度等によシ異なるが、一般に数1
0μ以下であることが要求され、とくにポリエチレンテ
レフタレートの場合には0.5〜10μの範囲にあるこ
とが必要とされる。しかるに、かように薄層の被膜を移
動冷却ロール表面に設けることは一般に極めて困難であ
り、とくに対象とする熱可塑性樹脂について最適な厚み
に被膜厚をコントロールしたり、製造条件の変更に対応
して被膜厚をコントロールしたシすることは不可能に近
いため、事実上このような方法によって所望の品質を有
する熱可塑性樹脂フィルムを得ることは困難であった。However, in this method, the thermally conductive liquid ultra-thin film on the moving cooling roll cools down by evaporation and absorption of thermoplastic resin by the time the moving cooling roll is reused (when the cooling roll makes one rotation). However, since this amount of consumption is generally extremely small, the coating thickness must be extremely thin. The thickness of this film varies depending on the type of thermoplastic resin to be used, the temperature of the moving cooling roll, etc., but it is generally several 1
It is required to be 0μ or less, and in particular, in the case of polyethylene terephthalate, it is required to be in the range of 0.5 to 10μ. However, it is generally extremely difficult to provide such a thin coating on the surface of a moving cooling roll, and it is especially difficult to control the coating thickness to the optimum thickness for the target thermoplastic resin or to respond to changes in manufacturing conditions. Since it is nearly impossible to control the film thickness by using such a method, it has been practically difficult to obtain a thermoplastic resin film having the desired quality by such a method.
また同様の考え方に基くと思われる方法として、特開昭
49−99160号公報に開示された方法が知られてい
る。この方法は沸点が150〜220℃で常温における
表面張力が50 dyne/crn以下であるアルコー
ル類を移動冷却ロール表面に塗布し、この口−ル表面に
溶融状態の線状ポリエステル樹脂を押出し、冷却成形せ
んとするものである。Furthermore, as a method that is believed to be based on a similar concept, a method disclosed in Japanese Patent Application Laid-open No. 49-99160 is known. In this method, alcohols with a boiling point of 150 to 220°C and a surface tension of 50 dyne/crn or less at room temperature are applied to the surface of a moving cooling roll, and a molten linear polyester resin is extruded onto the surface of this roll and cooled. It is intended to be molded.
しかしながら、この方法で用いられるアルコール類は沸
点が150〜220℃と蒸発しにくいため、蒸発による
アルコール類の消費が少なく、その結果、前述した英国
特許第1,312,519号明細書に開示された方法と
同様に被膜厚を極めて薄くする必要があり、現実的には
その実施に極めて大きな問題を伴なうという欠陥があっ
た。However, since the alcohols used in this method have a boiling point of 150 to 220°C and are difficult to evaporate, consumption of alcohols by evaporation is small, and as a result, the method disclosed in British Patent No. 1,312,519 mentioned above Similar to the method described above, it is necessary to make the coating thickness extremely thin, and in reality, this method has the drawback of being extremely difficult to implement.
本発明の目的は、上述した従来の欠点を解消し、溶融樹
脂膜の両端部の不安定な収縮流動を防止し、膜両端の冷
却ロール上での確実な固定を図り、両者間の密着性を向
上させ、溶融樹脂膜と冷却ロール間の空気の巻き込みを
抑制し、フィルムにおける厚みムラやシワをなくし、低
光沢、低透明性という問題を解消することのできる、熱
可塑性樹脂フィルムの製造方法を提供することにある。The purpose of the present invention is to eliminate the above-mentioned conventional drawbacks, prevent unstable shrinkage and flow at both ends of a molten resin film, securely fix both ends of the film on a cooling roll, and improve the adhesion between the two. A method for producing a thermoplastic resin film that improves the temperature, suppresses air entrainment between the molten resin film and the cooling roll, eliminates uneven thickness and wrinkles in the film, and solves the problems of low gloss and low transparency. Our goal is to provide the following.
本発明のもう一つの目的は、とくに高速成形時や薄膜フ
ィルム成形時における従来の問題を解決した熱可塑性樹
脂フィルムの製造方法を提供することにある。Another object of the present invention is to provide a method for producing a thermoplastic resin film that solves the conventional problems particularly during high-speed molding and thin film molding.
本発明の上記目的は1、溶融した熱可塑性樹脂をダイか
ら冷却ロール面上に押出してフィルムを製造する方法に
おいて、上記冷却ロールがフィルム巾の両端部に相当す
る部分に40〜250メツシュ、深さ10〜250ミク
ロンの網の目状の彫刻部を有し、かつ該彫刻部の総計巾
がダイ巾の多くとも10チであり、さらに同彫刻部に液
体塗布装置から液体が供給されていることを特徴とする
熱可塑性樹脂フィルムの製造方法によって、達成される
。The above objects of the present invention are as follows: 1. In a method of manufacturing a film by extruding a molten thermoplastic resin from a die onto the surface of a cooling roll, the cooling roll has a mesh of 40 to 250 mesh at a depth corresponding to both ends of the film width. It has a net-like engraved part with a diameter of 10 to 250 microns, and the total width of the engraved part is at most 10 inches of the die width, and furthermore, a liquid is supplied to the engraved part from a liquid application device. This is achieved by a method for producing a thermoplastic resin film characterized by the following.
また本発明の前記目的は、前記冷却ロールに施された彫
刻部に液体を供給したのち過剰な液体をドクターナイフ
により除去することを特徴とする熱可塑性樹脂フィルム
の製造方法によって、達成される。Further, the above-mentioned object of the present invention is achieved by a method for producing a thermoplastic resin film, characterized in that after supplying liquid to the engravings formed on the cooling roll, excess liquid is removed using a doctor knife.
本発明において用いられる熱可塑性樹脂は、公、知のも
のなら全て使用可能であり、たとえばポリエチレン、ポ
リプロピレン等のポリオレフィン樹脂、−リエチレンテ
レフタレート、ポリブチレンテレフタレート等のポリエ
ステル樹脂、ポリヘキサメチレンアジパミド、ポリ−ε
−カプラミド、ポリ−11−アミノウンデカミドおよび
これらの共重合体、ブレンド物のポリアミド樹脂、ポリ
スチレン樹脂、ポリメチルメタアクリレート等のアクリ
ル樹脂、ポリアセタール、ポリカーゴネート、ポリスエ
ニレンオキ°ナイド、ボリアリレート、ポリサルホン、
ポリエーテルサルホン、ポリフェニレンサルファイド、
ポリイミド、ポリアミドイミド、ぼりエーテルイミド等
のポリイミド類、ポリエーテルケトンなどがある。As the thermoplastic resin used in the present invention, any publicly known thermoplastic resin can be used, such as polyolefin resins such as polyethylene and polypropylene, polyester resins such as -lyethylene terephthalate and polybutylene terephthalate, polyhexamethylene adipamide, Poly-ε
- Capramide, poly-11-aminoundecamide and their copolymers, blends of polyamide resins, polystyrene resins, acrylic resins such as polymethyl methacrylate, polyacetals, polycarbonates, polyenylene oxynide, polyethylene arylate, polysulfone,
polyether sulfone, polyphenylene sulfide,
Examples include polyimide, polyamideimide, polyimide such as etherimide, and polyetherketone.
熱可塑性樹脂はダイから冷却ロール面上に押出されるが
、本発明では、その冷却ロールがフィルム巾の両端部に
相当する部分に網の目状彫刻部を有していなければなら
ない。これを第1図で説明すると、図中、lはTダイで
あり、2は溶融状の熱可塑性樹脂フィルム、3が冷却ロ
ールで、この冷却ロール3のフィルム巾の両端部に相当
する部分には、たとえばグラビアロールと同様な網の目
状彫刻部4が施されている。そしてこの彫刻部に液体塗
布装置から水などの液体が均一に供給される。このよう
にすると、フィルム両端部と冷却ロールの密着性が向上
し、溶融フィルムと冷却ロール間の不均一な空気の巻き
込を未然に防止することができる。The thermoplastic resin is extruded from a die onto the surface of a cooling roll, and in the present invention, the cooling roll must have a mesh-like engraved portion at portions corresponding to both ends of the film width. To explain this with reference to Figure 1, in the figure, l is a T-die, 2 is a molten thermoplastic resin film, and 3 is a cooling roll. For example, a net-like engraving portion 4 similar to that of a gravure roll is provided. A liquid such as water is uniformly supplied to this engraving portion from a liquid applicator. In this way, the adhesion between both ends of the film and the cooling roll is improved, and uneven air entrainment between the molten film and the cooling roll can be prevented.
さらに冷却ロールの彫刻部に塗布した液体がロール中心
へ移行するのを防ぐため、たとえばグラビヤロールを例
にとれば第2図0)(ロ)に示す如くドクターナイフ5
を冷却ロール面上に設け、塗布した液体を均一にすると
ともにその高さがロール面より高くならないよう余分な
液体を除去することが必要である。Furthermore, in order to prevent the liquid applied to the engraved part of the cooling roll from migrating to the center of the roll, for example, in the case of a gravure roll, a doctor knife is used as shown in Figure 2 (0) (b).
It is necessary to provide a cooling roll on the surface of the cooling roll, to make the applied liquid uniform, and to remove excess liquid so that the height of the applied liquid is not higher than the roll surface.
因みに冷却ロールに液体を塗布し溶融フィルムとの密着
性を高めるという方法は特開昭49−9916号、特開
昭55−44804号等の公報に開示されているが、こ
れらの方法では塗布した液体の除去の問題がある上、液
体がフィルムのロールの間でつぶされて次第にロール中
心へ移行し、冷却ムラが生じるという問題がちシ、こう
した問題は本発明によって解決される。Incidentally, a method of applying a liquid to a cooling roll to increase the adhesion with the molten film is disclosed in Japanese Patent Application Laid-Open Nos. 49-9916 and 55-44804. In addition to the problem of liquid removal, the liquid tends to be crushed between the rolls of film and gradually migrate to the center of the rolls, resulting in uneven cooling.These problems are solved by the present invention.
本発明に用いる液体は、沸点が50℃(常温)以上で、
粘度が200センチストークス(37,8℃)以下であ
ることが好ましい。液体の沸点が50℃未満では揮発性
が高くて十分な効果が得られないばかシではなく、使用
する液体によっては環境を汚染するという問題がある。The liquid used in the present invention has a boiling point of 50°C (normal temperature) or higher,
Preferably, the viscosity is 200 centistokes (37.8° C.) or less. If the boiling point of the liquid is less than 50° C., it is highly volatile and not only is it impossible to obtain sufficient effects, but also there is a problem that depending on the liquid used, it may pollute the environment.
また、粘度が200センチストークスよシ高い場合は、
フィルムが冷却ロールから引き剥がされるとき大きな抵
抗となるので好ましくない。このような液体としては、
たとえば水、アセトン、エタノール、鉱油、植物油等が
あげられる。Also, if the viscosity is higher than 200 centistokes,
This is undesirable since it creates a large resistance when the film is peeled off from the chill roll. Such a liquid is
Examples include water, acetone, ethanol, mineral oil, vegetable oil, etc.
冷却ロールに施す彫刻部は、網の目の形状に左右されな
い。たとえばフィルム厚み、成形速度、使用する液体に
よって円、楕円、四角形、六角形などが採用できる。彫
刻部の粗さは成形スピード、液体の粘度等によシ選択す
べきであるが、40〜250メツシュ、深さ10〜25
0ミクロンの範囲が必要である。この範囲を外れる場合
は液体の塗布全が過多あるいは過小となシ、本発明の効
果が得られない。彫刻部の総計巾はダイ巾の多くとも1
0チ必要で、0.5〜10チの範囲が好ましい。The engravings made on the cooling roll are not affected by the shape of the mesh. For example, a circle, ellipse, square, hexagon, etc. can be adopted depending on the film thickness, molding speed, and liquid used. The roughness of the engraving should be selected depending on the molding speed, viscosity of the liquid, etc., but it should be 40 to 250 mesh, 10 to 25
A range of 0 microns is required. If the amount is outside this range, the amount of liquid applied will be too much or too little, and the effects of the present invention will not be obtained. The total width of the engraving part is at most 1 of the die width.
0 inches is required, and the range of 0.5 to 10 inches is preferable.
彫刻部の総計巾が10%を越える場合は、フィルムの有
効な巾が狭くなるなど生産性の点で好ましくない。また
彫刻部の巾はフィルム巾の両端部で同−巾でも異なった
巾でもよい。If the total width of the engraved portion exceeds 10%, it is unfavorable from the viewpoint of productivity, as the effective width of the film becomes narrow. Further, the width of the engraved portion may be the same or different at both ends of the film width.
以下、実施例をあげて本発明をさらに詳細に説明する。 Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例1
ぼりプロピレン(kfFllo)を樹脂温度250℃で
Tダイ押出装置(押出機65聾φ、ダイ巾1000m、
リップ間隔0.5 vm )を用いて冷却ロール面上(
20℃)に押出した。Example 1 Foripropylene (kfFlo) was extruded at a resin temperature of 250°C using a T-die extrusion device (extruder 65mm diameter, die width 1000m,
on the cooling roll surface (with a lip spacing of 0.5 vm)
20°C).
冷却ロールとしては300φの鏡面仕上げロール面上に
60メツシュ、深さ170μの網の目状彫刻部をフィル
ム巾の両端部に相当する部分に20づつ施したものを使
用し、彫刻部にはドクターナイフをあてがった。The cooling roll used was a 300φ mirror-finished roll surface with 60 meshes and 20 net-like engravings of 170μ in depth on each side of the film width, and a doctor was used on the engravings. I put a knife on it.
上記彫刻部に液体塗布装置から20℃の水〔沸点100
℃、粘度約0.660センチストークス(37,8℃)
〕を供給し、引取速度75 m/it+inで厚さ20
μのフィルムを得た。Water at 20℃ [boiling point 100
°C, viscosity approximately 0.660 centistokes (37.8 °C)
] at a take-up speed of 75 m/it+in to a thickness of 20 mm.
A film of μ was obtained.
実施例2
網の目状彫刻部のメツシュを100.深さを100μと
したこと以外は実施例1と同様にして厚さ20μのフィ
ルムを成形した。Example 2 The mesh of the mesh engraving part was 100. A film with a thickness of 20 μm was molded in the same manner as in Example 1 except that the depth was 100 μm.
実施例3
網の目状彫刻部のメツシュを100、深さを100μと
し、液体として沸点が350℃以上の留分からなる。粘
度が約32センチストークス(37,8℃)の鉱油(飽
和炭化水素)を用いた以外は、実施例1と同様にして厚
さ20μのフィルムを成形した。Example 3 The mesh of the mesh-like engravings was 100 mm, the depth was 100 μm, and the liquid was composed of a fraction with a boiling point of 350° C. or higher. A film having a thickness of 20 μm was formed in the same manner as in Example 1, except that mineral oil (saturated hydrocarbon) having a viscosity of about 32 centistokes (37.8° C.) was used.
比較例1
冷却ロールとして彫刻部を設けていない300φの鏡面
仕上げロールを用い、さらにドクターナイフを用いなか
ったこと以外は(実施例1と同様の位置に水を供給)、
実施例1と同様にしてフィルムを成形し、厚さ20μの
フィルムを得た。Comparative Example 1 A 300φ mirror finish roll without engravings was used as the cooling roll, and a doctor knife was not used (water was supplied to the same position as in Example 1).
A film was molded in the same manner as in Example 1 to obtain a film with a thickness of 20 μm.
比較例2
彫刻部に水を供給しないこと以外は比較例1と同様にし
てフィルムを成形し、厚さ20μのフィルムを得た。Comparative Example 2 A film was molded in the same manner as Comparative Example 1 except that water was not supplied to the engraved portion, and a film with a thickness of 20 μm was obtained.
比較例3
ドクターナイフを使用しないこと以外は、実施例1と同
様にして厚さ20μのフィルムを成形した。Comparative Example 3 A film with a thickness of 20 μm was molded in the same manner as in Example 1, except that a doctor knife was not used.
比較例4
網の目状彫刻部を30メツシュ、深さ300μとしたこ
と以外は、実施例1と同様にして厚さ20μのフィルム
を成形した。Comparative Example 4 A film with a thickness of 20 μm was molded in the same manner as in Example 1, except that the mesh-like engraving portion was 30 meshes and the depth was 300 μm.
比較例5
網の目状の彫刻部を300メツシュ、深さ5μとしたこ
と以外は、実施例1と同様にして厚さ20μのフィルム
を成形した。Comparative Example 5 A film with a thickness of 20 μm was molded in the same manner as in Example 1, except that the mesh-shaped engraving portion was 300 meshes and the depth was 5 μm.
以上、実施例1〜3および比較例1〜5で得られたフィ
ルムの性質を表1に示した。Table 1 shows the properties of the films obtained in Examples 1 to 3 and Comparative Examples 1 to 5.
表1
中溶融フィルムと冷却ロールとの密着性〔発明の効果〕
本発明によればダイから押出された溶融樹脂膜が冷却ロ
ールに接し冷却される過程において、溶融樹脂膜を冷却
ロールに均一に接触させることができ、さらに彫刻部か
ら液体を塗布するためドクターナイフによシ余分な液体
を容易に除去することができ、そのため液面が冷却ロー
ル面よシはとんど高くならず、溶融樹脂膜と液体が接触
した際液体が押しつぶされてロール中心へと゛移行する
現象を未然に防ぐことができる。その結果、高速成形時
や薄膜フィルムの成形時においても、溶融樹脂膜と冷却
ロール間の空気のまき込みを十二分に、押えることがで
き、両者間の密着性を向上させることができるので、厚
みムラやシワ、低光沢、低透明性、冷却斑の発生といっ
た問題のない良好なフィルムを得ることが可能になった
。Table 1 Adhesion between the medium molten film and the cooling roll [Effects of the invention] According to the present invention, in the process in which the molten resin film extruded from the die contacts the cooling roll and is cooled, the molten resin film is uniformly applied to the cooling roll. Furthermore, since the liquid is applied from the engraved area, excess liquid can be easily removed using a doctor knife. Therefore, the liquid level is never higher than the cooling roll surface, and the melting This can prevent the liquid from being crushed and transferred to the center of the roll when the resin film comes into contact with the liquid. As a result, even during high-speed molding or thin film molding, the entrainment of air between the molten resin film and the cooling roll can be sufficiently suppressed, and the adhesion between the two can be improved. It became possible to obtain a good film without problems such as uneven thickness, wrinkles, low gloss, low transparency, and occurrence of cooling spots.
図面は本発明方法を実施するだめの代表的な装置の概略
構成図であり、第1図は上面図、第2図(イ)は側面図
、第2図(ロ)は斜視図である。
1・・・ダイ、2・・・溶融樹脂膜、3・・・冷却ロー
ル、4・・・網の目状彫刻部。The drawings are schematic diagrams of a typical apparatus for carrying out the method of the present invention; FIG. 1 is a top view, FIG. 2(a) is a side view, and FIG. 2(b) is a perspective view. DESCRIPTION OF SYMBOLS 1... Die, 2... Molten resin film, 3... Cooling roll, 4... Net-like engraving part.
Claims (2)
に押出してフィルムを製造する方法において、上記冷却
ロールがフィルム巾の両端部に相当する部分に40〜2
50メッシュ、深さ10〜250ミクロンの網の目状彫
刻部を有し、かつ該彫刻部の総計巾がダイ巾の多くとも
10%であり、さらに同彫刻部に液体塗布装置から液体
が供給されていることを特徴とする熱可塑性樹脂フィル
ムの製造方法:(1) In a method of manufacturing a film by extruding a molten thermoplastic resin from a die onto the surface of a cooling roll, the cooling roll has a 40 to
It has a net-like engraving part of 50 mesh and a depth of 10 to 250 microns, and the total width of the engraving part is at most 10% of the die width, and the engraving part is supplied with liquid from a liquid coating device. A method for producing a thermoplastic resin film characterized by:
たのち過剰な液体をドクターナイフにより除去すること
を特徴とする特許請求の範囲第(1)項記載の熱可塑性
樹脂フィルムの製造方法:(2) The method for producing a thermoplastic resin film according to claim (1), characterized in that after supplying liquid to the engravings formed on the cooling roll, excess liquid is removed using a doctor knife. :
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61167883A JPS6325016A (en) | 1986-07-18 | 1986-07-18 | Manufacture of thermoplastic resin film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61167883A JPS6325016A (en) | 1986-07-18 | 1986-07-18 | Manufacture of thermoplastic resin film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6325016A true JPS6325016A (en) | 1988-02-02 |
Family
ID=15857845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61167883A Pending JPS6325016A (en) | 1986-07-18 | 1986-07-18 | Manufacture of thermoplastic resin film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6325016A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002022304A1 (en) * | 2000-09-13 | 2002-03-21 | Baerlocher Gmbh | Tool surfaces comprising defined microstructures for eliminating deposits |
-
1986
- 1986-07-18 JP JP61167883A patent/JPS6325016A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002022304A1 (en) * | 2000-09-13 | 2002-03-21 | Baerlocher Gmbh | Tool surfaces comprising defined microstructures for eliminating deposits |
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