JPS61123520A - Manufacture of plastic film improved in slip property - Google Patents
Manufacture of plastic film improved in slip propertyInfo
- Publication number
- JPS61123520A JPS61123520A JP59245814A JP24581484A JPS61123520A JP S61123520 A JPS61123520 A JP S61123520A JP 59245814 A JP59245814 A JP 59245814A JP 24581484 A JP24581484 A JP 24581484A JP S61123520 A JPS61123520 A JP S61123520A
- Authority
- JP
- Japan
- Prior art keywords
- film
- plastic
- resin
- inorganic filler
- plastic 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
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、電子機材として適するフィルムに関するもの
であ妙、更に詳しくハ、滑ゆ性が改良され、かつ絶縁破
壊電圧の優れたフィルムの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a film suitable for electronic equipment. Regarding the method.
(従来の技術と発明が解決しようとする問題点)従来か
ら、コンデンサーの誘電体、プラスチック圧’を素子等
の電子機材用として洩々の用途にプラスチックフィルム
が使用されている。(Prior Art and Problems to be Solved by the Invention) Plastic films have been widely used in the past as dielectrics for capacitors and plastic film for electronic equipment such as elements.
特に電子機材用プラスチックフィルムは、小型化、高性
能下を得るため、最近までは益々薄いものが指向されて
いる。In particular, plastic films for electronic equipment have been becoming thinner and thinner in order to achieve smaller size and higher performance.
薄A電子機材用金属蒸着フィルムコンデンサーの製造に
あたっては、フィルムの物理的性能C厚み精(、強伸蜜
4)だけでなく、金属蒸着工程、細巾スリット工程、巻
回工程萼にお込で、フィルムとフィルムとの間やフィル
ムと接触する物体との間の滑りがよくないと、巻喉りが
困難となり、加工工程でしわ等のトラブルが発生し、製
品の歩留ゆが低下するため、滑りの改良されたフィルム
が不可欠となっている。In the production of metal-deposited film capacitors for thin A electronic equipment, we not only pay attention to the physical performance of the film C, thickness, and thickness, but also the metal deposition process, narrow slitting process, and winding process. If there is poor slippage between the films or between the film and the objects that come into contact with it, it will be difficult to roll the film, causing problems such as wrinkles during the processing process, and reducing the yield of the product. , films with improved slippage have become essential.
滑り性の改良方法としては、改良すべきフィルムvC環
機充填剤を6加してそのフィルム表面に適当な凹凸を付
与せしめる方法や、サンドブラスト等で表面に凹凸を付
与する方法等提案されている。As methods for improving the slipperiness, there have been proposed methods such as adding suitable unevenness to the surface of the film by adding vC ring filler to the film to be improved, and adding unevenness to the surface by sandblasting, etc. .
しかしながら前者の方法は、充填剤に含まれる微量な金
属・憤、分散剤が電気特性に望ましくない影響を与え、
また、コンデンサー用に一般的に使用されているポリエ
ステルフィルムやポ1)プロピレンフィルム等は、二軸
延伸加工が行なわれるため、上記問題点に加え、充填剤
の廻りにボイドが発生し、フィルムの絶縁破壊電圧を低
下?しめることとなる。また、ボイドの発生を回避する
ための鏝者の方法では、フィルム表面に多量の異物等が
付着するために洗滌等が必要となる。However, in the former method, trace amounts of metals, particles, and dispersants contained in the filler have an undesirable effect on the electrical properties.
In addition, polyester films and poly(1)propylene films that are commonly used for capacitors are biaxially stretched, so in addition to the above problems, voids are generated around the filler, and the film Reduce breakdown voltage? It will be concluded. Further, in the method of using a trowel to avoid the generation of voids, a large amount of foreign matter adheres to the surface of the film, so cleaning or the like is required.
かかる理由から、マーケットニーズに充分対応し得る解
決が要請されている。For these reasons, there is a need for a solution that can fully meet market needs.
(発明の概要)
本、明龜、上述。現状[1iみ、4り性。改良ヶれた、
か負絶縁破壊電圧の優れた電子機材用フィルムを提供す
ることを目的としてなされたものでちって、フィルムの
材料プラスチックと、環機充填剤を含有する樹脂を、前
記材料プラスチックの少なくとも接着側表面が溶融状態
下に接着せしめて積l−フィルムを形成し、次いでこれ
を剥離することを特徴とする滑り性の改良されたプラス
チックフィルムの製造法を提供するものである。(Summary of the Invention) The present invention, clearly described above. Current situation [1i, 4ri. Improved,
The purpose of this film is to provide a film for electronic equipment with excellent negative dielectric breakdown voltage, and the film material plastic and a resin containing a ring filler are added to at least the adhesion side surface of the plastic material. The present invention provides a method for producing a plastic film with improved slipperiness, which comprises adhering under molten conditions to form a laminated film, which is then peeled off.
本発明によるときは、無機充填剤を含む樹弓旨1―が添
加された無機充填剤により凹凸が形成され、これがプラ
スチックフィルム表面に転写されると共に、核フィルム
自体には無機充填剤を含まない為に、−軸又は二軸に延
伸し薄膜化してもボイド等の発生のない絶縁破壊電圧の
優れたフィルムが得られる。According to the present invention, unevenness is formed by the inorganic filler to which the inorganic filler is added, and this is transferred to the surface of the plastic film, and the core film itself does not contain the inorganic filler. Therefore, even if the film is thinned by stretching in the -axis or biaxial direction, a film with excellent dielectric breakdown voltage without generation of voids etc. can be obtained.
C問題点を解決するための手段)
本発明のプラスチックフィルムを形成するために材料と
して用いられるプラスチックは@に制限がなく、ポリエ
チレン、ポリプロピレン、エチレン−フロピレン共重合
体、エチレン−ブテン−1共重合体等ポリオレフィン系
、ポリアミド、ポリエステル、ポIIK化ビニール、ポ
リフェニレンエーテル、ポリ7フ化ビニリデン、ポリメ
チルペンテン等フィルム成形用に用いられる熱可塑性樹
脂を用Aることができる。C) The plastic used as a material to form the plastic film of the present invention is not limited, and includes polyethylene, polypropylene, ethylene-propylene copolymer, and ethylene-butene-1 copolymer. Thermoplastic resins used for film molding, such as polyolefins, polyamides, polyesters, poly(IIK) vinyl, polyphenylene ether, polyvinylidene heptafluoride, and polymethylpentene, can be used.
本発明は、フィルムの材料プラスチックと、無機充填剤
を含有する樹脂を、フィルムの材料用グラスチックの少
なくとも接着側表面が溶融状標下に積層される。In the present invention, a plastic material for the film and a resin containing an inorganic filler are laminated with at least the adhesive side surface of the glass material for the film in a molten state.
材料プラスチックと積層用樹脂の接着は、積層後の各工
程においてfil一部が剥離しない程度であゆ、かつ蒸
着1穐、スリットエ穆での剥離時に被11層の一部が成
形体に残ったり、逆に成形体の一部が被覆層に残ったり
しない程度の密着積、1i状態が望ましい。The adhesion between the plastic material and the resin for lamination is such that a part of the film does not peel off in each step after lamination, and a part of the layer 11 remains on the molded body when peeled off during vapor deposition and slit removal. On the contrary, it is desirable that the adhesion area is 1i such that no part of the molded body remains on the coating layer.
ここでいう密着積層状態とは、例えば樹脂A及び他のl
et脂Bの界百から剥離し得る程度の積層を云う。The closely laminated state here refers to, for example, resin A and other lubricants.
It refers to the lamination to the extent that it can be peeled off from the surface of etal fat B.
積層に用いる樹脂は、プラスチックフィルム用檄唸と互
いに接着性の不良な樹脂を用い積層すればよい。互いに
接着性の不良な樹脂としては、例えば、プラスチックの
臨界表面張力を比較することによって選択される。As for the resin used for lamination, it is sufficient to use a resin that has poor adhesion to the resin film for plastic film. Resins with poor adhesion to each other are selected, for example, by comparing the critical surface tensions of plastics.
本発明者等の知見では、臨界表面張力(ratの差1表
−1参照)が4.0以上のプラスチックを選ぶことによ
り、良好な剥離性を有する積層物を得ることができる。According to the findings of the present inventors, a laminate having good releasability can be obtained by selecting a plastic having a critical surface tension (see rat difference 1 Table 1) of 4.0 or more.
(以下余白)
表−1
例えば、表−1よりポリプロピレン/ポリエステル、ポ
リプロピレン/ポリスチレン、ポリエチレン/ポリフッ
化ビニリデン、ボ11プロピレン/ポリフッ化ビニリデ
ン等の組合せが望ましい。京らに積層後、延伸する場合
には、臨界表面張力以外にも延伸温度、延伸倍率、熱処
理温度等の条件を考慮して組合せる必要がある。(The following is a blank space) Table 1 For example, from Table 1, combinations such as polypropylene/polyester, polypropylene/polystyrene, polyethylene/polyvinylidene fluoride, and polypropylene/polyvinylidene fluoride are desirable. In the case of stretching after laminating Kyo et al., it is necessary to consider and combine conditions such as stretching temperature, stretching ratio, heat treatment temperature, etc. in addition to critical surface tension.
積層用樹脂に添加される無機充填剤としては、粉末状の
雲機物であり、たとえば、炭酸カル7ウム、塩基性炭酸
マグネシウム、硅酸カルシウム、硅酸マグネシウム、水
酸化アルミニウム、水酸化マグネシウム、酸化カルシウ
ム、酸化マグネシウム、酸化チタン、クレー、タルク等
プラスチックに分散可能な無機物質の粉末であり、これ
ら単独もしくは2f!!i以上の混合物であってもよい
。The inorganic filler added to the laminating resin is a powdery mineral filler, such as calcium carbonate, basic magnesium carbonate, calcium silicate, magnesium silicate, aluminum hydroxide, magnesium hydroxide, It is a powder of inorganic substances such as calcium oxide, magnesium oxide, titanium oxide, clay, and talc that can be dispersed in plastics, and these can be used alone or in combination with 2f! ! It may be a mixture of i or more.
本発明にm−る無機充填剤の平均粒径は、とくに限定さ
れるものではないが、0.1〜20μの範囲のものから
撰択するのがよAo
前記プラスチックと前記無機充填剤とから積1脅樹脂組
成物を調整するには、界面活性剤、金属石m類、高級脂
肪酸等の表面処理剤を、また必要に芯じて熱安定剤、光
安定剤、顔料等をさらに添加シテ、バンバリー、ロール
、プラペンf−、−軸押出機等公知の方法で溶融混練す
ればよい。The average particle size of the inorganic filler used in the present invention is not particularly limited, but it is preferably selected from the range of 0.1 to 20μ. To prepare the resin composition, surface treatment agents such as surfactants, metal stones, and higher fatty acids are added, and if necessary, heat stabilizers, light stabilizers, pigments, etc. are further added. The melt-kneading may be carried out using a known method such as a Banbury extruder, a Banbury extruder, a roll extruder, a plastic extruder, or an extruder.
この際、組成物中に前記無機充填剤を0.1重量%以上
であればよく、被覆積層後延伸する場合には、延伸性が
阻害される為60重量壬以下が好ましい。さらに好まし
くは0.5〜30重量係含有するように調整してやれば
よい。At this time, it is sufficient that the inorganic filler is contained in the composition in an amount of 0.1% by weight or more, and in the case of stretching after coating and lamination, the amount of the inorganic filler is preferably 60% by weight or less since stretchability is inhibited. More preferably, the content may be adjusted to 0.5 to 30% by weight.
積層は、使用されるプラスチックの1il@成形体の形
状、延伸加工の有無等によって適宜の手段がとられるが
、フィルムの材料プラスチックと積層用meをダイス内
で溶融密着させた状態で押出す方法が望ましい、、また
、別の押出機から押出された積層樹脂フィルム上に材料
プラスチックをフィルム状に押出し、圧延ロールで圧延
密着する方法を採用することもできる。また薄いフィル
ムを得ようとするときは、積層したフィルムを一軸又は
二軸方向に延伸した後各層を剥離することにより得るこ
とができる。For lamination, an appropriate method is taken depending on the shape of the plastic molded body used, the presence or absence of stretching, etc., but it is a method of extruding the plastic material of the film and the me for lamination in a state in which they are melted and adhered in a die. It is also possible to extrude the plastic material into a film onto a laminated resin film extruded from another extruder, and then roll it into tight contact with a rolling roll. Further, when a thin film is to be obtained, it can be obtained by stretching the laminated film in a uniaxial or biaxial direction and then peeling off each layer.
積層用樹脂は、材料プラスチックの少なくとも片面に積
層され、目的に応じて両面に積1することもできる。The laminating resin is laminated on at least one side of the plastic material, and can be laminated on both sides depending on the purpose.
また、積層する際には、11i1WIJ樹脂が接触する
側の材料プラスチック表面は溶融状態下にあることが必
要である。Furthermore, when laminating, the surface of the plastic material that comes into contact with the 11i1WIJ resin needs to be in a molten state.
溶融状態下とは、材料プラスチックが可塑性をもつ状態
を云い非品性樹脂についてはガラス転移点以上の状態を
指す。The molten state refers to a state in which the plastic material has plasticity, and in the case of non-grade resins, it refers to a state at or above the glass transition point.
なお、本発明は、薄肉フィルムの成形に適するが、フィ
ルムの厚さには制限がなく、肉厚のものにも適用するこ
とができる。従って、本発明のフィルム:は、一般にシ
ートと称される肉厚物も含む。Note that although the present invention is suitable for forming thin films, there is no limit to the thickness of the film, and it can also be applied to thick films. Therefore, the film of the present invention also includes thick-walled materials commonly referred to as sheets.
これらの方法で得られた積I−されたフィルムは、剥離
されながら蒸着して巻取られる工程、コンデンサー用に
細巾にス11ットして巻取る工程、巻回機でコンデンサ
ー素子に巻取る工程等の加工工程において、しわ等の発
生のない安定生産できるものであった。また、得られた
プラスチック成形体の絶縁破壊電圧も大巾に改善された
ものであった。The laminated film obtained by these methods undergoes a step of being vapor-deposited and wound up while being peeled off, a step of rolling it up into a thin strip for use in a capacitor, and a step of winding it around a capacitor element using a winding machine. Stable production was possible without the occurrence of wrinkles in the processing steps such as the stripping process. Furthermore, the dielectric breakdown voltage of the obtained plastic molded article was also greatly improved.
以下に実施例をもって本発明をさらに具体的に説明する
。The present invention will be explained in more detail with reference to Examples below.
実施例1〜4
平均粒径が5μの竹原化学社製炭酸カルシウム「ホワイ
トシールWS−toolと三菱油化社製ポリプロピレン
(メルトフローv −トs、s ? /l。Examples 1 to 4 Calcium carbonate "White Seal WS-tool" manufactured by Takehara Chemical Co., Ltd. with an average particle size of 5 μ and polypropylene manufactured by Mitsubishi Yuka Co., Ltd. (melt flow v-s, s?/l.
分)とをバンバリーミキサ−にて溶融混練し、ペレタイ
ザーにて炭酸カルシウム含有量0.5重量%、5重量憾
及び20重量憾のペレット状の熱可塑性樹脂組成物を得
た。また、同様にして、平均粒径が1μの竹原化学社要
炭酸カルシウム[ホワイトシールWS−3KJを用いて
炭酸カルシウム含有量5重量幅の組成物を得た。) were melt-kneaded in a Banbury mixer, and pelletized thermoplastic resin compositions having a calcium carbonate content of 0.5% by weight, 5% by weight, and 20% by weight were obtained using a pelletizer. Further, in the same manner, a composition having a calcium carbonate content of 5 weight range was obtained using Takehara Chemical Co., Ltd.'s calcium carbonate [White Seal WS-3KJ] having an average particle size of 1 μm.
次に658押出機に上記組成物を、30Fl押出機にペ
ンウォルト社#T KYNA凡)ボ11コツ化ビニ11
デンを夫々供給1.、てその両表面に前記組成物を各層
の厚さが50 / 10 / 50 gの三1−構造物
となるように涜141シた。Next, the above composition was transferred to a 658 extruder, and the above composition was transferred to a 30F extruder using Pennwalt Co., Ltd.
Supply each den 1. Then, the above composition was applied to both surfaces of the structure so that each layer had a thickness of 50/10/50 g to form a 31-structure.
これを120℃′r:5倍に軸延伸を行な・4各1脅の
厚さが夫々10/2/1 (1μの三1ilJ11遣延
伸物を得た。This was axially stretched at 120° C.'r: 5 times to obtain three 11 il J11 stretched products each having a thickness of 10/2/1 (1 μm).
同様にして、積11樹脂に炭酸カルシウムを含まない三
層構造物及びこれの延伸物を得た。また、前記被覆層及
びプラスチック成形体であるPVI)Fに平均粒径5μ
の前記無機充填剤を5重t%を含有してなる三層構造延
伸物を得た。In the same manner, a three-layer structure containing no calcium carbonate in the resin of Product 11 and a stretched product thereof were obtained. In addition, the coating layer and the plastic molded body (PVI) F have an average particle size of 5 μm.
A three-layer stretched product containing 5% by weight of the above-mentioned inorganic filler was obtained.
Claims (1)
樹脂を、前記材料プラスチックの少なくとも接着側表面
が溶融状態下に接着せしめて積層フィルムを形成し、次
いでこれを剥離することを特徴とする滑り性が改良され
たプラスチックフィルムの製造法。A laminated film is formed by adhering a plastic material of the film and a resin containing an inorganic filler while at least the adhesion side surface of the plastic material is in a molten state, and then this is peeled off. Improved method of manufacturing plastic film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59245814A JPS61123520A (en) | 1984-11-20 | 1984-11-20 | Manufacture of plastic film improved in slip property |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59245814A JPS61123520A (en) | 1984-11-20 | 1984-11-20 | Manufacture of plastic film improved in slip property |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61123520A true JPS61123520A (en) | 1986-06-11 |
Family
ID=17139244
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59245814A Pending JPS61123520A (en) | 1984-11-20 | 1984-11-20 | Manufacture of plastic film improved in slip property |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61123520A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005169935A (en) * | 2003-12-12 | 2005-06-30 | Sanko Plastics Kk | Laminated film, thin poyvinylidene fluoride film, electronic component, and production method for the component |
WO2018139264A1 (en) * | 2017-01-25 | 2018-08-02 | 株式会社クレハ | Vinylidene fluoride resin film |
WO2018139262A1 (en) * | 2017-01-25 | 2018-08-02 | 株式会社クレハ | Vinylidene fluoride resin film |
-
1984
- 1984-11-20 JP JP59245814A patent/JPS61123520A/en active Pending
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005169935A (en) * | 2003-12-12 | 2005-06-30 | Sanko Plastics Kk | Laminated film, thin poyvinylidene fluoride film, electronic component, and production method for the component |
WO2018139264A1 (en) * | 2017-01-25 | 2018-08-02 | 株式会社クレハ | Vinylidene fluoride resin film |
WO2018139262A1 (en) * | 2017-01-25 | 2018-08-02 | 株式会社クレハ | Vinylidene fluoride resin film |
KR20190065361A (en) * | 2017-01-25 | 2019-06-11 | 가부시끼가이샤 구레하 | Vinylidene fluoride resin film |
CN110036062A (en) * | 2017-01-25 | 2019-07-19 | 株式会社吴羽 | Vinylidene resin film |
JPWO2018139262A1 (en) * | 2017-01-25 | 2019-07-25 | 株式会社クレハ | Vinylidene fluoride resin film |
JPWO2018139264A1 (en) * | 2017-01-25 | 2019-08-08 | 株式会社クレハ | Vinylidene fluoride resin film |
US10988586B2 (en) | 2017-01-25 | 2021-04-27 | Kureha Corporation | Vinylidene fluoride resin film |
CN110036062B (en) * | 2017-01-25 | 2021-04-30 | 株式会社吴羽 | Vinylidene fluoride resin film |
US11136440B2 (en) | 2017-01-25 | 2021-10-05 | Kureha Corporation | Vinylidene fluoride resin film |
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