JPH0222048A - Composite polyester film - Google Patents
Composite polyester filmInfo
- Publication number
- JPH0222048A JPH0222048A JP17306788A JP17306788A JPH0222048A JP H0222048 A JPH0222048 A JP H0222048A JP 17306788 A JP17306788 A JP 17306788A JP 17306788 A JP17306788 A JP 17306788A JP H0222048 A JPH0222048 A JP H0222048A
- Authority
- JP
- Japan
- Prior art keywords
- film
- composite
- polyester film
- deposited
- layer
- 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
- 229920006267 polyester film Polymers 0.000 title claims abstract description 23
- 239000002131 composite material Substances 0.000 title abstract description 27
- -1 poly(1,4-cyclohexylene dimethylene terephthalate Chemical compound 0.000 claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 10
- 239000002184 metal Substances 0.000 claims abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 abstract description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 7
- 239000012770 industrial material Substances 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 229920006254 polymer film Polymers 0.000 abstract description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000011701 zinc Substances 0.000 abstract description 2
- 229910052725 zinc Inorganic materials 0.000 abstract description 2
- 238000007740 vapor deposition Methods 0.000 abstract 4
- 239000000853 adhesive Substances 0.000 abstract 2
- 230000001070 adhesive effect Effects 0.000 abstract 2
- 239000004411 aluminium Substances 0.000 abstract 1
- VEIOBOXBGYWJIT-UHFFFAOYSA-N cyclohexane;methanol Chemical group OC.OC.C1CCCCC1 VEIOBOXBGYWJIT-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 26
- 229920000139 polyethylene terephthalate Polymers 0.000 description 18
- 239000005020 polyethylene terephthalate Substances 0.000 description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 230000008018 melting Effects 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 239000008188 pellet Substances 0.000 description 7
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- LZFNKJKBRGFWDU-UHFFFAOYSA-N 3,6-dioxabicyclo[6.3.1]dodeca-1(12),8,10-triene-2,7-dione Chemical compound O=C1OCCOC(=O)C2=CC=CC1=C2 LZFNKJKBRGFWDU-UHFFFAOYSA-N 0.000 description 1
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical compound O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、複合ポリエステルフィルムに関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a composite polyester film.
更に詳しくは、主として工業材料用の複合ポリエステル
フィルムに関するものである。More specifically, the present invention mainly relates to composite polyester films for industrial materials.
[従来の技術]
従来、複合ポリエステルフィルムとしては、ポリエチレ
ンテレフタレートフィルムの片面にポリエチレンイソフ
タレートと、ポリエチレンテレフタレートを共重合した
フィルムを複合し、蒸着金属を設けたフィルムや、特公
昭58−12153号に示されるように、特定の結晶融
解熱を有するフィルムを複合したフィルムが知られてい
る。[Prior Art] Conventionally, composite polyester films include films in which a polyethylene terephthalate film is composited with a film made by copolymerizing polyethylene isophthalate and polyethylene terephthalate on one side, and a vapor-deposited metal is provided on one side, and a film is disclosed in Japanese Patent Publication No. 58-12153. As shown, composite films of films having a specific heat of crystal fusion are known.
[発明が解決しようとする課題]
しかし、上記従来の複合ポリエステルフィルムは、蒸着
膜の付着力が悪い、静電容量変化率が大きいという問題
があった。[Problems to be Solved by the Invention] However, the above-mentioned conventional composite polyester film has problems in that the adhesion of the deposited film is poor and the rate of change in capacitance is large.
本発明は、かかる問題点を改善し、蒸着膜の付着力及び
静電容量変化率の優れた複合ポリエステルフィルムを提
供することを目的とする。An object of the present invention is to improve such problems and provide a composite polyester film with excellent adhesion of a deposited film and excellent capacitance change rate.
[課題を解決するため手段]
本発明は、ポリエステルフィルムの少なくとも片面にポ
リ(1,4−シクロヘキシレンジメチレンテレフタレー
ト)フィルムが設けられ、かつ該ポリ(1,4−シクロ
ヘキシレンジメチレンテレフタレート)の表面に蒸着金
属が設けられてなる複合ポリエステルフィルムを特徴と
するものである。[Means for Solving the Problems] The present invention provides a polyester film with a poly(1,4-cyclohexylene dimethylene terephthalate) film provided on at least one side thereof, and a poly(1,4-cyclohexylene dimethylene terephthalate) film. It is characterized by a composite polyester film with vapor-deposited metal on its surface.
本発明におけるポリエステルフィルムとは、ポリマの結
合連鎖の50モル%以上、好ましくは75モル%以上が
エステル結合で結ばれている重合体あるいは共重合体か
らなるフィルムであり、ポ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、ポリエチレンナフタレー
ト、ポリエチレン・ビス(2−クロルフェノキシ)エタ
ン−4゜4′−ジカルボキシレートフィルムなどが代表
例でおるが、本発明に特に好ましいのは、ポリエチレン
テレフタレートフィルムである。ここでいうポリエチレ
ンテレフタレートとは、エチレンテレフタレート単位が
80モル%以上を占めているものである。換言すれば、
20モル%を越さない範囲で、他の分子単位、例えばエ
チレンイソフタレト、ブチレンテレフタレート、エチレ
ンアジベト、アルキレングリコール、ポリアルキレング
リコールなどが共重合されていてもよい。このポリエチ
レンテレフタレート中には、公知の添加剤、例えば無機
微粒子、着色防止剤などが添加されていてもよい。The polyester film in the present invention is a film made of a polymer or copolymer in which 50 mol% or more, preferably 75 mol% or more of the polymer chains are connected by ester bonds, and includes polyethylene terephthalate,
Typical examples include polybutylene terephthalate, polyethylene naphthalate, and polyethylene bis(2-chlorophenoxy)ethane-4°4'-dicarboxylate film, but polyethylene terephthalate film is particularly preferred in the present invention. The polyethylene terephthalate mentioned here is one in which ethylene terephthalate units account for 80 mol% or more. In other words,
Other molecular units such as ethylene isophthalate, butylene terephthalate, ethylene adibet, alkylene glycol, polyalkylene glycol, etc. may be copolymerized within a range not exceeding 20 mol %. This polyethylene terephthalate may contain known additives, such as inorganic fine particles and color inhibitors.
なお、本発明のポリエステルフィルムとは、上記ポリエ
ステルフィルムを二軸方向に延伸して、配向せしめたも
のである。The polyester film of the present invention is obtained by biaxially stretching and orienting the above-mentioned polyester film.
本発明のポリ(1,4−シクロヘキシレンジメチレンテ
レフタレート)[以下、PCTと略称する]フィルムと
は、シクロヘキサンジメタツール単位が50モル%、好
ましくは70モル%以上からなるエステル結合で結ばれ
ている共重合体、混合体からなるフィルムである。シク
ロヘキサンジメタツール単位のジオール成分としては、
エチレングリコール、ジエチレングリコールなどであり
、酸成分としてはテレフタル酸、イソフタル酸、ナフタ
リンジカルボン酸などが代表例であるが、特に好ましい
のは70モル%以上のテレフタル酸である。The poly(1,4-cyclohexylene dimethylene terephthalate) [hereinafter abbreviated as PCT] film of the present invention is a poly(1,4-cyclohexylene dimethylene terephthalate) [hereinafter abbreviated as PCT] film in which cyclohexane dimetatool units are bonded by ester bonds consisting of 50 mol% or more, preferably 70 mol% or more. It is a film made of a copolymer or mixture of The diol component of the cyclohexane dimetatool unit is:
Typical examples of the acid component include terephthalic acid, isophthalic acid, naphthalene dicarboxylic acid, and the like, with 70 mol% or more of terephthalic acid being particularly preferred.
また、該ポリマの融点は好ましくは245°C以上、よ
り好ましくは255°C以上である。このポリマ中には
、公知の添加剤、例えば無機微粒子、着色防止剤などが
添加されていてもよい。なお、本発明のPCTフィルム
の平均表面粗さは、好ましくは0.005〜0.05μ
m1より好ましくは0.01〜0.04μmである。ま
た、フィルム中の外部粒子含有量は、平均粒径0.1〜
0゜6μmの大きさの粒子が0.05〜0.5%含有さ
れているのが好ましい。Further, the melting point of the polymer is preferably 245°C or higher, more preferably 255°C or higher. Known additives, such as inorganic fine particles and anti-coloring agents, may be added to this polymer. Note that the average surface roughness of the PCT film of the present invention is preferably 0.005 to 0.05μ.
m1 is more preferably 0.01 to 0.04 μm. In addition, the external particle content in the film has an average particle size of 0.1 to
It is preferable that particles having a size of 0.6 μm are contained in an amount of 0.05 to 0.5%.
本発明の蒸着金属とは、金属の種類は特に限定されるも
のではないカベアルミニウム、亜鉛、銅、錫などの低融
点金属、あるいはクロム、ニッケル、鉄、チタンなどの
高融点金属のいずれも用いることができ、蒸着する膜の
厚さは、0.02〜0゜2μm程度の範囲が好ましい。The vapor-deposited metal of the present invention is not particularly limited in type, and may be a low melting point metal such as aluminum, zinc, copper, or tin, or a high melting point metal such as chromium, nickel, iron, or titanium. The thickness of the film to be vapor-deposited is preferably in the range of about 0.02 to 0.2 μm.
本発明にお(プる複合ポリエステルフィルムとは、上記
ポリエステルフィルムの片面あるいは両面に、蒸着金属
が設けられたPCTフィルムを複合したものである。蒸
着金属が片面だけに設けられていでもよい。複合ポリエ
ステルフィルムの各層の厚みは、ポリエステルフィルム
層は1〜25μmが好ましく、PC下フィルム層は、0
.2〜5μm1より好ましくは0.5〜3μmで′必る
。PC丁フィルム層の厚みが上記範囲より小さくなると
、耐湿下の静電容量の変化率が大きくなり、また上記範
囲より大きいと、ポリマーフィルムが襞間を、起こした
り、機械的特性が低下したりする。The composite polyester film used in the present invention is a composite of a PCT film in which a vapor-deposited metal is provided on one or both sides of the above-mentioned polyester film.The vapor-deposited metal may be provided on only one side.Composite The thickness of each layer of the polyester film is preferably 1 to 25 μm for the polyester film layer, and 0 to 25 μm for the PC lower film layer.
.. The thickness is preferably 0.5 to 3 μm, more preferably 0.5 to 3 μm. If the thickness of the PC film layer is smaller than the above range, the rate of change in capacitance under humidity resistance will increase, and if it is larger than the above range, the polymer film may develop creases or its mechanical properties may deteriorate. do.
次に本発明の複合ポリエステルフィルムの製造方法につ
いて説明する。Next, the method for manufacturing the composite polyester film of the present invention will be explained.
ポリエチレンテレフタレート(以下、PETと略称する
)及びPCHのペレットを各々別の押出機に供給して2
85°Cで溶融押出し、各々の溶融体をT型口金の中で
合流せしめて、PET/PC下の2層からなるシートを
つくる。このシートを100’Cに加熱して長手方向に
3.2倍延伸し、−旦冷却した後、再度110’Cに加
熱して幅方向に3.3倍延伸し、緊張状態のまま200
’Cの熱風中で5秒間熱処理する。Pellets of polyethylene terephthalate (hereinafter abbreviated as PET) and PCH were each fed to separate extruders.
Melt extrusion was carried out at 85° C. and the respective melts were combined in a T-shaped nozzle to form a sheet consisting of two layers under PET/PC. This sheet was heated to 100'C, stretched 3.2 times in the longitudinal direction, cooled once, heated again to 110'C, stretched 3.3 times in the width direction, and kept under tension for 200
Heat treatment in hot air at 'C for 5 seconds.
熱処理したフィルムを室温まで徐冷して、PET層10
μm5PCT層1μmの複合ポリエステルフィルムを得
る。この複合ポリエステルフィルムのPCT層表面に常
法に従って、アルミニウムを0.05μmの厚さに蒸着
する。The heat-treated film is slowly cooled to room temperature to form the PET layer 10.
A composite polyester film with 5 μm and 1 μm PCT layer is obtained. Aluminum is vapor-deposited to a thickness of 0.05 μm on the surface of the PCT layer of this composite polyester film according to a conventional method.
こうしてできた複合ポリエステルフィルムは、コンデン
サや包装などの工業材料用途に使用される。The composite polyester film produced in this way is used for industrial material applications such as capacitors and packaging.
[発明の効果]
本発明は、ポリエステル/PCTの複合フィルムのPC
T層に蒸着を行なったため、蒸着膜のイ」着、蒸着膜の
配向、蒸着膜の成長状態がポリエステル層に蒸着する場
合と異なり、緻密になったものと推定される。このため
、蒸着膜の付着力が向上し、静電容量変化率が減少した
ものと思われる。[Effect of the invention] The present invention provides a polyester/PCT composite film
It is presumed that because the T layer was vapor-deposited, the deposition of the vapor-deposited film, the orientation of the vapor-deposited film, and the growth state of the vapor-deposited film were different from those in the case of vapor-depositing on the polyester layer, and were denser. This seems to be the reason why the adhesion of the deposited film improved and the rate of change in capacitance decreased.
また、ポリエステル層との複合フィルムでおるため、ポ
リエステル層の機械的特性が保持されたまま、他の特性
が向上できる利点があり、工業材料用途に適する。Furthermore, since it is a composite film with a polyester layer, it has the advantage that other properties can be improved while maintaining the mechanical properties of the polyester layer, making it suitable for industrial material applications.
[特性の測定方法及び効果の評価方法](1) 蒸着
膜の付着力
恒温槽に水を入れ、65°Cの温水にし、これに15分
間蒸着フィルムを浸漬し、蒸着膜の消失度合を観察した
。蒸着膜の変化がないものを○、少し変化したものを△
、蒸着膜がほとんど消失してしまったものを×とし、3
段階で付着力を評価した。[Method for measuring characteristics and evaluating effectiveness] (1) Adhesion of vapor deposited film Fill water in a constant temperature bath, make it warm to 65°C, soak the vapor deposited film in it for 15 minutes, and observe the degree of disappearance of the vapor deposited film. did. ○ means that there is no change in the deposited film, △ means that there is a slight change
, those in which the deposited film has almost disappeared are marked as ×, and 3
Adhesion was evaluated in stages.
(2)静電容量変化率
蒸着したフィルムからコンデンサ素子(1,5μF)を
つくり50’C,95%RHで、35Vの直流印加の条
件で2000時間経過したときの静電容量変化率(ΔC
/C)(%)を測定した。(2) Capacitance change rate A capacitor element (1.5 μF) was made from the deposited film, and the capacitance change rate (ΔC
/C) (%) was measured.
(3〉 機械的特性
JIS C2318−72の方法で破断強伸度を求め
た。また、伸びと応力からヤング率を算出した。(3> Mechanical Properties Breaking strength and elongation were determined by the method of JIS C2318-72. Young's modulus was also calculated from the elongation and stress.
「実施例]
以下、実施例に基づいて、本発明の実施態様を説明する
。"Examples" Hereinafter, embodiments of the present invention will be described based on Examples.
実施例1
PETのペレット(融点260’C1平均粒径O0,3
μmの乾式シリカ0.1重量%を含有)及び酸成分とし
てテレフタル酸85モル%、イソフタル酸15モル%、
ジオール成分としてシクロヘキサンジメタツール100
%で共重合したPCT(融点270’Cで平均粒径0.
4μmの乾式シリカ0.15%を含有)のペレットを各
々別の押出機に供給して、290’Cで溶融押出し、各
々の溶融体をT型口金の中で合流させて、PET層表面
下の2層からなるシートを作った。このシートを100
’Cで長手方向に3.5倍、110°Cで幅方向に3.
5倍延伸し、200’Cで5秒間熱処理し、PET層9
μm、PCT層1μmの複合フィルムを得た。PCTフ
ィルムの表面粗さは、0.03μmであった。この複合
フィルムのPCT層表面にアルミニウムを0.05μm
の厚さに蒸着した。Example 1 PET pellets (melting point 260'C1 average particle size O0,3
85 mol% of terephthalic acid, 15 mol% of isophthalic acid,
Cyclohexane dimetatool 100 as diol component
% copolymerized PCT (melting point 270'C, average particle size 0.
Pellets of 4 μm dry silica (containing 0.15% silica) were each fed into a separate extruder and melt extruded at 290'C, and each melt was combined in a T-type nozzle to form a layer under the surface of the PET layer. A sheet consisting of two layers was made. This sheet is 100
3.5 times in the longitudinal direction at 'C and 3.5 times in the width direction at 110°C.
Stretched 5 times and heat treated at 200'C for 5 seconds to form PET layer 9
A composite film with a PCT layer of 1 μm and a PCT layer of 1 μm was obtained. The surface roughness of the PCT film was 0.03 μm. Aluminum is applied to the surface of the PCT layer of this composite film to a thickness of 0.05 μm.
It was deposited to a thickness of .
できた蒸着複合フィルムの評価結果を第1表に示すが、
蒸着膜の付着力、静電容量変化率ともに良好な結果を示
した。Table 1 shows the evaluation results of the vapor-deposited composite film.
Good results were shown in both the adhesion of the deposited film and the rate of change in capacitance.
比較例1
PETのペレット(融点260°C1平均粒径0゜3μ
mの乾式シリカ0.1重量%を含有)及びイソフタル1
117.5モル%で共重合したPET(融点210°C
〉のペレットを各々別の押出機に供給して、280’C
で溶融押出し、2層シートを作った。このシートを90
’Cで長手方向に3.5倍、100°Cで幅方向に3.
5倍延伸して180°Cで5秒間熱処理し、PET層9
μm、共重合PET層1μmの複合フィルムを得た。こ
の複合フィルムの共重合PET層表面にアルミニウムを
0゜05μmの厚さに蒸着した。Comparative Example 1 PET pellets (melting point 260°C1 average particle size 0°3μ
containing 0.1% by weight of dry silica) and isophthale 1
PET copolymerized with 117.5 mol% (melting point 210°C
> pellets were each fed to separate extruders and heated at 280'C.
A two-layer sheet was made by melt extrusion. This sheet is 90
3.5 times in the longitudinal direction at 'C, 3.5 times in the width direction at 100°C.
Stretched 5 times and heat treated at 180°C for 5 seconds to form PET layer 9
A composite film having a thickness of 1 μm and a copolymerized PET layer of 1 μm was obtained. Aluminum was deposited on the surface of the copolymerized PET layer of this composite film to a thickness of 0.05 μm.
できた蒸着複合フィルム評価結果を第1表に示すが、付
着力、静電容量変化率ともに実施例1より悪くなってい
る。The evaluation results of the vapor-deposited composite film are shown in Table 1, and both the adhesion and the rate of change in capacitance were worse than in Example 1.
比較例2
実施例1のPE下のペレットのみを280’Cで溶融押
出し、単層シートを作った。このシートを90’Cで長
手方向に3.5倍、95°Cで幅方向に3.5倍延伸し
、200 ’Cで5秒間熱処理し10μmの単層フィル
ムを得た。このフィルムのアルミニウムを0.05μm
の厚さに蒸着した。Comparative Example 2 Only the pellet under PE of Example 1 was melt extruded at 280'C to make a single layer sheet. This sheet was stretched 3.5 times in the longitudinal direction at 90'C and 3.5 times in the width direction at 95°C, and heat treated at 200'C for 5 seconds to obtain a 10 μm single layer film. The aluminum of this film is 0.05μm
It was deposited to a thickness of .
できた蒸着フィルムの評価結果を第1表に示すが付着力
、静電容量変化率ともに悪い結果である。The evaluation results of the deposited film are shown in Table 1, and both the adhesion and the rate of change in capacitance were poor.
比較例3
実施例1の原料(但し、PCT共重合ペレットに乾式シ
リカを含有しないもの)を用いて、同様に延伸し、PE
T層2μm、PCT層8μmの2層複合フィルムを得た
。PCTフィルの表面粗さは0.003μmであった。Comparative Example 3 The raw material of Example 1 (however, the PCT copolymer pellets did not contain dry silica) was stretched in the same manner, and PE
A two-layer composite film having a T layer of 2 μm and a PCT layer of 8 μm was obtained. The surface roughness of the PCT film was 0.003 μm.
このフィルムにアルミニウムを0.05μmの厚さに蒸
着した。Aluminum was deposited on this film to a thickness of 0.05 μm.
できた蒸着複合フィルムの評価結果を第1表に示すが、
付着力、静電容量変化率ともに実施例1よりも悪く、機
械的特性が劣っており、使用しにくいものであった。Table 1 shows the evaluation results of the vapor-deposited composite film.
Both adhesion and capacitance change rate were worse than Example 1, mechanical properties were inferior, and it was difficult to use.
第1表Table 1
Claims (1)
−シクロヘキシレンジメチレンテレフタレート)フィル
ムが設けられ、かつ該ポリ(1,4−シクロヘキシレン
ジメチレンテレフタレート)の表面に蒸着金属が設けら
れてなることを特徴とする複合ポリエステルフィルム。At least one side of the polyester film is coated with poly(1,4
- cyclohexylene dimethylene terephthalate) film, and a vapor-deposited metal is provided on the surface of the poly(1,4-cyclohexylene dimethylene terephthalate).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17306788A JPH0222048A (en) | 1988-07-11 | 1988-07-11 | Composite polyester film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17306788A JPH0222048A (en) | 1988-07-11 | 1988-07-11 | Composite polyester film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0222048A true JPH0222048A (en) | 1990-01-24 |
Family
ID=15953595
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17306788A Pending JPH0222048A (en) | 1988-07-11 | 1988-07-11 | Composite polyester film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0222048A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1070539C (en) * | 1994-04-15 | 2001-09-05 | 东丽株式会社 | Metallized films and capacitors containing the same |
-
1988
- 1988-07-11 JP JP17306788A patent/JPH0222048A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1070539C (en) * | 1994-04-15 | 2001-09-05 | 东丽株式会社 | Metallized films and capacitors containing the same |
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