JPH0892400A - Surface treatment for thermoplastic resin sheet - Google Patents
Surface treatment for thermoplastic resin sheetInfo
- Publication number
- JPH0892400A JPH0892400A JP6229676A JP22967694A JPH0892400A JP H0892400 A JPH0892400 A JP H0892400A JP 6229676 A JP6229676 A JP 6229676A JP 22967694 A JP22967694 A JP 22967694A JP H0892400 A JPH0892400 A JP H0892400A
- Authority
- JP
- Japan
- Prior art keywords
- film
- ethylene
- vinyl alcohol
- corona discharge
- alcohol copolymer
- 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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Physical Vapour Deposition (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Laminated Bodies (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、食品、電子部品等を保
護するために用いられるガスバリア性の優れた包装用樹
脂成形品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin molded product for packaging which is used for protecting foods, electronic parts and the like and has an excellent gas barrier property.
【0002】[0002]
【従来の技術】食品、電子工業部品等をフィルム、容器
で包装し酸素の透過を抑制することにより内容物の酸化
を防止し、品質を長期間保つことが提案されている。例
えば、特公昭53−12953号、特開平4−3535
32号公報には、厚さが5〜300μmのポリエチレン
テレフタレート、セロファン、ナイロン、ポリプロピレ
ン、ポリエチレン等のフレキシブルプラスチックフィル
ムの少なくとも片面に一般式SixOy(x=1,2,
y=0,1,2,3)なる組成の珪素酸化物の厚さ10
0〜3000オングストロームの透明ガラス質薄膜層を
設けた高度の耐透気性と耐透湿性を有する透明フレキシ
ブルプラスチックフィルムが開示されている。2. Description of the Related Art It has been proposed to wrap foods, electronic industrial parts and the like in a film or a container to suppress oxygen permeation to prevent oxidation of the contents and maintain quality for a long time. For example, Japanese Patent Publication No. 53-12953, JP-A-4-3535.
No. 32 discloses a general formula SixOy (x = 1, 2, on at least one surface of a flexible plastic film such as polyethylene terephthalate, cellophane, nylon, polypropylene, or polyethylene having a thickness of 5 to 300 μm.
thickness of silicon oxide having a composition of y = 0, 1, 2, 3) 10
Disclosed is a transparent flexible plastic film having a high degree of air permeation resistance and moisture permeation resistance, which is provided with a transparent vitreous thin film layer of 0 to 3000 angstrom.
【0003】また、特開昭63−23794号公報に
は、上記フレキシブルプラスチックフィルムの少なくと
も一方の面に、In,Sn,Zn,ZrおよびTiから
なる群から選ばれた一種の金属の金属酸化物がスパッタ
リングにより形成され、更にこの上に透明なヒートシー
ル性樹脂膜がコートされた透明なガスバリア性樹脂フィ
ルムが開示されている。フィルム素材がポリエチレンテ
レフタレート、ナイロン、セロファンのような極性基を
有する樹脂である時は、フィルムと無機酸化膜との密着
力が十分で、ガスバリア性も良好である。Further, in Japanese Patent Laid-Open No. 63-23794, a metal oxide of one kind of metal selected from the group consisting of In, Sn, Zn, Zr and Ti on at least one surface of the flexible plastic film. There is disclosed a transparent gas-barrier resin film in which a transparent heat-sealable resin film is coated thereon by sputtering. When the film material is a resin having a polar group such as polyethylene terephthalate, nylon, and cellophane, the film and the inorganic oxide film have sufficient adhesion and good gas barrier properties.
【0004】しかし、ポリプロピレン、ポリエチレンの
ような極性基を有しないポリオレフィンの成形品の表面
に、上記のような無機酸化物からなる蒸着膜を形成させ
ても、実用に耐えられる安定したガスバリア性は得られ
ない。すなわち、ポリオレフィン成形品と薄膜との密着
力が弱いので、この蒸着物にヒートシール性を付与する
ために成形品を構成するポリオレフィンの融点よりも低
い融点を有するヒートシール性樹脂をラミネートする場
合や、このラミネート物を用い、製袋や蓋シールの二次
加工を行う際や、これら袋を用いたり、容器内に収容物
を充填し、更にはレトルト殺菌する際に外部応力や熱が
成形品に加わって無機酸化薄膜がポリオレフィン成形品
より剥離し、ガスバリア性が低下し、実用に耐えない問
題がある。However, even if a vapor-deposited film made of the above-mentioned inorganic oxide is formed on the surface of a molded product of a polyolefin having no polar group such as polypropylene or polyethylene, it has a stable gas barrier property that can withstand practical use. I can't get it. That is, since the adhesion between the polyolefin molded product and the thin film is weak, when laminating a heat-sealable resin having a melting point lower than the melting point of the polyolefin constituting the molded product in order to impart heat-sealing property to this vapor deposit, , When this laminate is used for secondary processing such as bag making or lid sealing, or when these bags are used, or when the contents are filled in a container and further sterilized by retort, external stress or heat is applied to the molded product. In addition, the inorganic oxide thin film is peeled off from the polyolefin molded product, the gas barrier property is deteriorated, and there is a problem that it cannot be put to practical use.
【0005】[0005]
【発明が解決しようとする課題】本発明は、無機酸化薄
膜が蒸着されたオレフィン系樹脂成形品で、ガスバリア
性に優れ、更にこれの二次加工時や使用時に無機酸化薄
膜が剥離せず、ガスバリア性が低下しない樹脂成形品を
提供することを目的とするものである。DISCLOSURE OF THE INVENTION The present invention is an olefin resin molded article having an inorganic oxide thin film deposited thereon, which is excellent in gas barrier properties, and the inorganic oxide thin film does not peel off during secondary processing or use of the product. It is an object of the present invention to provide a resin molded product that does not deteriorate in gas barrier property.
【0006】[0006]
【課題を解決するための手段】本発明は、オレフィン系
樹脂を溶融押出して得た未延伸のフィルムを縦方向に延
伸したのち、60〜100℃に加熱し、30〜100w
・分/m2 のコロナ放電処理を行い、ついで該縦延伸フ
ィルムのコロナ処理面にエチレン含量が20〜45モル
%のエチレン−ビニルアルコール共重合体の塗液をコー
ティングし、乾燥後、テンターで横方向に延伸し、更に
このコーティング面に30〜100w・分/m2 のコロ
ナ放電処理を行って得た積層フィルムのエチレン−ビニ
ルアルコール共重合体の延伸フィルム面上に、無機酸化
物の蒸着膜を形成した構造のガスバリア性の付与された
樹脂成形品を提供するものである。According to the present invention, an unstretched film obtained by melt-extruding an olefin resin is stretched in the machine direction and then heated to 60 to 100 ° C. for 30 to 100 w.
Min / m 2 corona discharge treatment is performed, and then the corona-treated surface of the longitudinally stretched film is coated with an ethylene-vinyl alcohol copolymer coating solution having an ethylene content of 20 to 45 mol%, dried and then in a tenter. Stretching in the transverse direction and further subjecting this coating surface to a corona discharge treatment of 30 to 100 w · min / m 2 for vapor deposition of an inorganic oxide on the stretched film surface of the ethylene-vinyl alcohol copolymer of the laminated film obtained. It is intended to provide a resin molded article having a gas barrier property having a film-formed structure.
【0007】[0007]
【作用】エチレン−ビニルアルコール共重合体と無機酸
化物を組み合わせることにより良好なガスバリア性が得
られ、更にエチレン−ビニルアルコール共重合体の塗膜
の薄い延伸物のコロナ放電処理物が有するアルコール性
水酸基とカルボキシル基の存在により、基材と無機酸化
物蒸着膜の密着性がより強固となる。[Function] By combining an ethylene-vinyl alcohol copolymer and an inorganic oxide, a good gas barrier property can be obtained, and further, the alcoholicity of a corona discharge treated product of a thin stretched film of the ethylene-vinyl alcohol copolymer is obtained. Due to the presence of the hydroxyl group and the carboxyl group, the adhesion between the substrate and the inorganic oxide vapor deposition film becomes stronger.
【0008】[0008]
【発明の具体的な説明】基材層用のオレフィン系樹脂は
プロピレンホモポリマー、プロピレン・エチレン共重合
体、プロピレン・ブテン−1共重合体、プロピレン・4
−メチルペンテン−1共重合体等のプロピレン系樹脂、
分岐低密度ポリエチレン、リニア−ポリエチレン等のエ
チレン系樹脂、あるいは、α,β−不飽和カルボン酸で
変性したオレフィン系樹脂が利用できる。これらは2種
以上混合して用いてもよいし、あるいは、積層して用い
てもよい。更に、抗ブロッキング剤、核剤、安定剤、滑
剤等を0.01〜2重量%含有していてもよい。DETAILED DESCRIPTION OF THE INVENTION The olefin resin for the base material layer is propylene homopolymer, propylene / ethylene copolymer, propylene / butene-1 copolymer, propylene / 4.
-Propylene-based resin such as methylpentene-1 copolymer,
Ethylene resins such as branched low-density polyethylene and linear polyethylene, or olefin resins modified with α, β-unsaturated carboxylic acid can be used. These may be used as a mixture of two or more kinds, or may be used by being laminated. Further, it may contain 0.01 to 2% by weight of an anti-blocking agent, a nucleating agent, a stabilizer, a lubricant and the like.
【0009】エチレン・ビニルアルコール共重合体の塗
液 塗液用のエチレン・ビニルアルコール共重合体は、エチ
レンが20〜45モル%、好ましくは25〜35モル
%、ビニルアルコールが80〜55モル%、好ましくは
75〜65モル%の共重合体であって、通常は、エチレ
ン(20〜45モル%)と酢酸ビニル(80〜55モル
%)との共重合体を苛性ソーダ、苛性カリ等のアルカリ
でケン化度が86モル%以上、好ましくは90〜100
%となるように加水分解して得られるものである。 Coating of ethylene / vinyl alcohol copolymer
The ethylene / vinyl alcohol copolymer for liquid coating liquid is a copolymer of ethylene of 20 to 45 mol%, preferably 25 to 35 mol%, and vinyl alcohol of 80 to 55 mol%, preferably 75 to 65 mol%. Usually, a copolymer of ethylene (20 to 45 mol%) and vinyl acetate (80 to 55 mol%) is treated with an alkali such as caustic soda or caustic so that the saponification degree is 86 mol% or more, preferably 90% or more. ~ 100
It is obtained by hydrolyzing so that the content becomes%.
【0010】ビニルアルコールが共重合体中に占める割
合が55モル%未満では、無機酸化物蒸着層との接着力
が十分でない。逆に、80モル%を越えるとフィルムの
延伸性が損なわれる。エチレン・ビニルアルコール共重
合体の融点は178〜205℃である。エチレン・ビニ
ルアルコール共重合体の塗液はエチレン・ビニルアルコ
ール共重合体を水、または水とエチレンアルコール、イ
ソプロピレンアルコール等のアルコールとの混合液に樹
脂固型分濃度が5〜50重量%となるように溶解するこ
とにより得られる。When the proportion of vinyl alcohol in the copolymer is less than 55 mol%, the adhesive force with the inorganic oxide vapor deposition layer is insufficient. On the contrary, when it exceeds 80 mol%, the stretchability of the film is impaired. The melting point of the ethylene / vinyl alcohol copolymer is 178 to 205 ° C. The coating liquid of the ethylene / vinyl alcohol copolymer is prepared by adding the ethylene / vinyl alcohol copolymer to water or a mixed liquid of water and an alcohol such as ethylene alcohol or isopropylene alcohol to have a resin solid content of 5 to 50% by weight. It is obtained by dissolving so that
【0011】塗液には乳化剤、帯電防止剤、ブロッキン
グ防止剤、粘度調整剤等の各種添加物を目的に応じて適
宜添加することができる。塗液の粘度は20℃で10〜
5,000センチポイズ、40℃で300〜60,00
0センチポイズ(B型粘度計)である。基材層用フィル
ムへのエチレン・ビニルアルコール共重合体の塗液の塗
布は、例えばグラビヤロール法、インバースロール法、
リバースロール法、エアナイフコート法、メタリングバ
ーコート法またはこれらの組み合わせによる各種コーテ
ィング方式を採用することができる。Various additives such as an emulsifier, an antistatic agent, an antiblocking agent, and a viscosity modifier can be appropriately added to the coating liquid according to the purpose. The viscosity of the coating solution is 10 at 20 ° C.
5,000 centipoise, 300-60,000 at 40 ° C
It is 0 centipoise (B-type viscometer). Application of the coating liquid of the ethylene / vinyl alcohol copolymer to the base layer film is performed by, for example, a gravure roll method, an inverse roll method,
Various coating methods such as a reverse roll method, an air knife coating method, a metalling bar coating method, or a combination thereof can be adopted.
【0012】塗布の厚みはウエット膜厚みで10〜60
μの範囲で、最終の延伸物の肉厚が0.05〜4μmと
なるように選択される。コーティングに用いる塗布液は
60〜100℃に加温して用いるのが好ましい。60℃
未満ではエチレン・ビニルアルコール共重合体の塗液の
適性粘度保持が困難の為、均一な塗布を得ることが難し
い、100℃を越えるとエチレン・ビニルアルコール共
重合体の塗液中の溶剤が蒸発し、粘度が上がりすぎ、均
一塗布が困難となる。The thickness of application is 10 to 60 in terms of wet film thickness.
In the range of μ, the thickness of the final stretched product is selected to be 0.05 to 4 μm. The coating liquid used for coating is preferably heated to 60 to 100 ° C. before use. 60 ° C
If it is less than 100, it is difficult to maintain the proper viscosity of the coating solution of ethylene / vinyl alcohol copolymer, so it is difficult to obtain a uniform coating. If it exceeds 100 ° C, the solvent in the coating solution of ethylene / vinyl alcohol copolymer evaporates. However, the viscosity becomes too high, making uniform coating difficult.
【0013】積層延伸フィルムの製造方法 本発明のガスバリア性フィルムは、前記オレフィン系樹
脂を、単層、または多層で、フィルム状に溶融押し出
し、この未延伸フィルムをロール群の周速差またはテン
ターを利用して2〜7倍縦方向に延伸したのち、該延伸
フィルムに加熱し、30〜100w・分/m2 のコロナ
放電処理を行い、該縦延伸フィルムのコロナ処理面にエ
チレン・ビニルアルコール共重合体の塗液をコーティン
グし、乾燥後、テンターで横方向に3.5〜12倍に延
伸し、更にこのコーティング面に30〜100w・分/
m2 のコロナ放電処理を行うことにより製造される。上
記前後のコロナ放電処理の量が30w・分/m2 未満で
はエチレン・ビニルアルコール共重合樹脂の塗膜にピン
ホールが発生したり、均一な塗膜が得られない。 Method for Producing Laminated Stretched Film In the gas barrier film of the present invention, the above-mentioned olefin resin is melt-extruded into a film in a single layer or a multilayer, and the unstretched film is subjected to a peripheral speed difference between roll groups or a tenter. After stretching in the machine direction 2 to 7 times in the longitudinal direction, the stretched film is heated and subjected to a corona discharge treatment of 30 to 100 w · min / m 2 and the corona-treated surface of the longitudinally stretched film is treated with ethylene / vinyl alcohol. After coating with a coating solution of the polymer, after drying, it is stretched in the transverse direction 3.5 to 12 times with a tenter, and further 30 to 100 w · min / min on this coating surface
It is manufactured by performing a corona discharge treatment of m 2 . If the amount of corona discharge treatment before and after the above is less than 30 w · min / m 2 , pinholes are generated in the coating film of the ethylene / vinyl alcohol copolymer resin, and a uniform coating film cannot be obtained.
【0014】逆に100w・分/m2 を越えると放電ス
パークが大きく、塗膜に白化筋模様が生じ、塗布ムラの
原因になる。コロナ放電処理前の加熱は、加熱金属ロー
ル、熱風オーブン、遠赤外ヒーター等が使用される。前
段の加熱は60〜100℃、後段の加熱は、20〜11
0℃、好ましくは80〜110℃である。後段のコロナ
放電処理量が30w・分/m2 未満では、エチレン・ビ
ニルアルコール共重合樹脂層と無機酸化物蒸着膜層との
密着性が劣り、また、100w・分/m2 越えるとブロ
ッキングしやすく、フィルムの白化ムラが生じ、外観の
劣るものとなる。On the other hand, when it exceeds 100 w · min / m 2 , discharge sparks are large and a whitening pattern is formed on the coating film, which causes uneven coating. For heating before the corona discharge treatment, a heating metal roll, a hot air oven, a far infrared heater or the like is used. The first-stage heating is 60 to 100 ° C, and the second-stage heating is 20 to 11
The temperature is 0 ° C, preferably 80 to 110 ° C. If the amount of corona discharge treatment in the latter stage is less than 30 w · min / m 2 , the adhesion between the ethylene / vinyl alcohol copolymer resin layer and the inorganic oxide vapor deposition film layer will be poor, and if it exceeds 100 w · min / m 2 , blocking will occur. It is easy to cause uneven whitening of the film, resulting in poor appearance.
【0015】積層延伸フィルムは、基材層が肉厚10〜
100μmの二軸延伸ポリオレフィンフィルムで表面層
が肉厚0.05〜4.0μmのエチレン・ビニルアルコ
ール共重合体の一軸延伸フィルムの積層物である。該積
層樹脂フィルムの総肉厚は10.05〜104μm、透
明度は霞み度(JIS K7105)5%以下、好まし
くは1〜3%である。The laminated stretched film has a base material layer having a thickness of 10 to 10.
It is a laminate of a uniaxially stretched film of an ethylene / vinyl alcohol copolymer having a thickness of 0.05 to 4.0 μm and a biaxially stretched polyolefin film of 100 μm in thickness. The total thickness of the laminated resin film is 10.05 to 104 μm, and the transparency is 5% or less, and preferably 1 to 3%, in the degree of haze (JIS K7105).
【0016】無機酸化物の蒸着 無機酸化物の蒸着した薄膜としては、SiOx ,SnO
x ,ZnOx ,IrO x 等の200〜4,000オング
ストローム、好ましくは300〜3,000オングスト
ロームのものが利用される。蒸着膜の厚み200〜4,
000オングストロームは、透明性、蒸着速度、ガスバ
リア性、フィルムの巻き取り性等から制約される。[0016]Inorganic oxide deposition As the thin film on which the inorganic oxide is deposited, SiO is used.x, SnO
x, ZnOx, IrO x200-4,000 ang of etc.
Strom, preferably 300-3,000 angstroms
ROHM's one is used. Vapor deposition film thickness 200-4
000 Å is for transparency, deposition rate, gas bar
It is restricted by the rear property and the film winding property.
【0017】蒸着法としては、高周波誘導加熱方式の蒸
着機内で成形品を真空下(1×10 -8〜1×106 トー
ル)で無機酸化物を蒸着する方法(特公昭53−129
63号);予め排気し、真空化した蒸着機内で揮発した
有機シリコン化合物、酸素及び不活性ガスを含むガス流
をマグネトロングロー放電によってプラズマを発生させ
てSiOx を該蒸着機内で成形品に蒸着させる方法(特
開昭64−87772号、USP4,557,946
号、USP4,599,678号)等がある。又、19
90年11月発刊の工業材料、第38巻、第14号の第
104〜105頁で、イオンプレーティング法、高周波
プラズマCVD法、電子ビーム(EB)蒸着法、スパッ
タリング法として分類され、その原理が紹介されてい
る。As the vapor deposition method, a high frequency induction heating method is used.
Molded product under vacuum (1 x 10 -8~ 1 × 106toe
Method for depositing an inorganic oxide (Japanese Patent Publication No. 53-129).
No. 63); volatilized in a vapor deposition machine which was evacuated and evacuated in advance.
Gas flow containing organosilicon compounds, oxygen and inert gas
To generate plasma by magnetron glow discharge
SiOxMethod of depositing the
Kai 64-87772, USP 4,557,946
No., USP 4,599,678) and the like. Also, 19
Industrial materials published in November 1990, Vol. 38, No. 14
Pages 104-105, ion plating method, high frequency
Plasma CVD method, electron beam (EB) vapor deposition method, spatter
It is classified as the Taling method and its principle is introduced.
It
【0018】[0018]
【実施例】以下、実施例により、本発明を詳細に説明す
るが、これにより本発明の範囲は特に限定されるもので
はない。 実施例1 押出機を用い、ポリプロピレン(MFR2.3g/10
分、融点164〜167℃)樹脂を210℃で溶融し、
Tダイよりシート状に押し出し、これを60℃に冷却
し、未延伸のシートを得た。この未延伸シートを周速の
異なる加熱ロール群からなる縦延伸機で、130℃の温
度で5倍に延伸し、続いて、この縦延伸シートを90℃
に加熱ロールで熱加温し、次いでコーティングする面側
を90w・分/m2 の条件でコロナ放電処理を施した。
次に、80℃に加熱したエチレン(29モル%)−ビニ
ルアルコール(71モル%)ランダム共重合樹脂(日本
合成化学工業(株)ソアノール30L(商品名);融点
188℃)塗布液(樹脂濃度30重量%)をメタリング
バーコーターを用いてウエット膜15μm厚さにコーテ
ィングし、搬送ローラを介して155℃のテンターオー
ブン内に導入し、横方向に10倍延伸し、160℃で熱
セットし、このフィルムを105℃に加温しコーティン
グ面にコロナ処理量50w・分/m2 になるようにコロ
ナ放電処理を行い、厚さ20μmのコーティングフィル
ム(コート層の厚さは0.45μm)を得た。The present invention will be described in detail below with reference to examples, but the scope of the present invention is not particularly limited thereby. Example 1 Using an extruder, polypropylene (MFR 2.3 g / 10
Min, melting point 164-167 ° C.) melt the resin at 210 ° C.,
The sheet was extruded from a T-die and cooled to 60 ° C. to obtain an unstretched sheet. This unstretched sheet was stretched 5 times at a temperature of 130 ° C. by a longitudinal stretching machine composed of a group of heating rolls having different peripheral speeds, and then this longitudinally stretched sheet was heated to 90 ° C.
Then, the surface side to be coated was subjected to corona discharge treatment under the condition of 90 w · min / m 2 .
Next, ethylene (29 mol%)-vinyl alcohol (71 mol%) random copolymer resin (Nippon Gosei Kagaku Kogyo Co., Ltd. Soarnol 30L (trade name); melting point 188 ° C.) coating liquid (resin concentration) heated to 80 ° C. 30% by weight) was coated to a thickness of 15 μm with a metalling bar coater, introduced into a tenter oven at 155 ° C. via a conveying roller, stretched 10 times in the transverse direction, and heat set at 160 ° C. Then, this film was heated to 105 ° C., and a corona discharge treatment was applied to the coated surface so that the corona treatment amount was 50 w · min / m 2, and a coating film having a thickness of 20 μm (coat layer thickness 0.45 μm) was obtained. Obtained.
【0019】このフィルムを、プラズマ蒸着装置(BP
−1;サムコインターナショナル研究所)内に置き、装
置内を1.33×10-4Paの減圧下にしたのち、ヘキ
サメチルジシロキサン3容量部、酸素3容量部、ヘリウ
ム20容量部、アルゴン13容量部の混合気体を同装置
内に導き、不平衡型マグネトロンよりグロー放電を行っ
てプラズマを発生させSiO2 蒸着させた。このSiO
2 蒸着積層延伸樹脂フィルムの酸素透過度を測定した。This film was applied to a plasma deposition device (BP
-1; Samco International Laboratories), and the inside of the apparatus under reduced pressure of 1.33 × 10 −4 Pa, hexamethyldisiloxane 3 parts by volume, oxygen 3 parts by volume, helium 20 parts by volume, argon 13 The mixed gas in the capacity part was introduced into the apparatus, and glow discharge was performed from the unbalanced magnetron to generate plasma to deposit SiO 2 . This SiO
2 The oxygen permeability of the vapor-deposited laminated stretched resin film was measured.
【0020】実施例2 ポリプロピレン(MFR2.3g/10分;融点165
〜170℃)樹脂と接着性樹脂;無水マレイン酸(0.
35重量%)グラフトポリプロピレン(MFR3g/1
0分;融点165〜170℃)を、別々の押出機で各々
220℃で溶融したものを一台の共押出ダイに供給し、
ダイ内で層状に重ね、これを押し出し、以下、実施例1
と同様にして縦方向に5倍延伸後、接着性樹脂側にコロ
ナ処理を施し、エチレン−ビニルアルコールランダム共
重合樹脂塗布液をコーティングし、横方向に10倍延伸
後、コロナ放電処理を施し、厚さ20μmの延伸フィル
ムを得た。このフィルムに実施例1と同様に、SiO2
を蒸着し、酸素透過度を測定した。Example 2 Polypropylene (MFR 2.3 g / 10 min; melting point 165)
~ 170 ° C) resin and adhesive resin; maleic anhydride (0.
35% by weight) Grafted polypropylene (MFR 3g / 1
0 min; melting point 165 to 170 ° C.) melted at 220 ° C. in separate extruders and fed to one coextrusion die,
Layered in a die and extruded, the following Example 1
In the same manner as above, after stretching 5 times in the longitudinal direction, corona treatment is applied to the adhesive resin side, ethylene-vinyl alcohol random copolymer resin coating liquid is coated, and after stretching 10 times in the transverse direction, corona discharge treatment is applied, A stretched film having a thickness of 20 μm was obtained. This film was coated with SiO 2 in the same manner as in Example 1.
Was vapor-deposited and the oxygen permeability was measured.
【0021】比較例1 エチレン・ビニルアルコール共重合樹脂の塗液を塗布し
ない及び前段のコロナ放電処理を行わない以外は、実施
例1と同様にして二軸延伸フィルムを製造し、SiO2
を蒸着し、酸素透過度を測定した。 比較例2 二軸延伸フィルムSiO2 を蒸着しない以外は、実施例
1と同様にして二軸延伸フィルムを製造し、酸素透過度
を測定した。Comparative Example 1 A biaxially stretched film was produced in the same manner as in Example 1 except that the coating liquid of ethylene / vinyl alcohol copolymer resin was not applied and the corona discharge treatment in the previous stage was not performed, and SiO 2 was used.
Was vapor-deposited and the oxygen permeability was measured. Comparative Example 2 A biaxially stretched film was produced in the same manner as in Example 1 except that the biaxially stretched film SiO 2 was not deposited, and the oxygen permeability was measured.
【0022】評価 (1)二次加工に対する変化 実施例1,2、および比較例1,2で得た二軸延伸フィ
ルムのSiO2 蒸着面、あるいはコロナ放電処理前に、
ラミネータ装置を用い、MFRが5g/10分、密度
0.922g/cm3 の低密度ポリエチレンを320℃
で20μmの肉厚のフィルム状にT−ダイより押し出
し、ラミネートした。このラミネート物の酸素透過率を
表1に示す。Evaluation (1) Change with respect to secondary processing The SiO 2 vapor-deposited surface of the biaxially stretched films obtained in Examples 1 and 2 and Comparative Examples 1 and 2 or before corona discharge treatment,
Using a laminator apparatus, MFR is 5 g / 10 min, a low density polyethylene having a density of 0.922g / cm 3 320 ℃
Was extruded from a T-die into a film having a thickness of 20 μm and laminated. The oxygen transmission rate of this laminate is shown in Table 1.
【0023】(2)外応力に対する変化 実施例1〜2、および比較例1〜2で得た二軸延伸フィ
ルム、および低密度ポリエチレンとのラミネートフィル
ムを、名立計器(株)製ゲルボテスターを用い、フィル
ムを筒状に丸めたのち、この筒の両端をテスターの把持
器具に固定し、10回、±90度回転ねじりの繰り返し
を行った後、酸素透過率を測定した。その測定値を表1
に示す。(2) Change with respect to external stress The biaxially stretched films obtained in Examples 1 and 2 and Comparative Examples 1 and 2 and the laminated film with low density polyethylene were used in a gelbot tester manufactured by Meitetsu Keiki Co., Ltd. After the film was rolled into a tubular shape, both ends of the tubular tube were fixed to a gripping device of a tester, and a twist of ± 90 ° was repeated 10 times, and then the oxygen transmission rate was measured. The measured values are shown in Table 1.
Shown in.
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【発明の効果】本発明の無機酸化物が蒸着した二軸延伸
フィルムは、二次加工時や使用時に、熱や力が加わって
もガスバリア性が低下しない樹脂成形品である。INDUSTRIAL APPLICABILITY The biaxially stretched film on which the inorganic oxide is vapor-deposited according to the present invention is a resin molded product which does not deteriorate in gas barrier property even when heat or force is applied during secondary processing or during use.
フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C09D 129/04 PEV C23C 14/10 8939−4K // B29K 23:00 B29L 9:00 Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI Technical display location C09D 129/04 PEV C23C 14/10 8939-4K // B29K 23:00 B29L 9:00
Claims (1)
延伸のフィルムを縦方向に延伸したのち、60〜100
℃に加熱し、30〜100w・分/m2 のコロナ放電処
理を行い、ついで該縦延伸フィルムのコロナ処理面にエ
チレン含量が20〜45モル%のエチレン−ビニルアル
コール共重合体の塗液をコーティングし、乾燥後、テン
ターで横方向に延伸し、更にこのコーティング面に30
〜100w・分/m2 のコロナ放電処理を行って得た積
層延伸フィルムのエチレン−ビニルアルコール共重合体
の延伸フィルム面上に、無機酸化物の蒸着膜を形成した
構造のガスバリア性の付与された樹脂成形品。1. An unstretched film obtained by melt-extruding an olefin resin is stretched in the machine direction, and then 60-100.
℃ heated to perform the corona discharge treatment of 30~100W · min / m 2, and then the ethylene content in the corona-treated surface of the vertical oriented film is 20 to 45 mole percent ethylene - a coating liquid of a vinyl alcohol copolymer After coating and drying, stretch in the transverse direction with a tenter,
A gas barrier property of a structure in which a vapor-deposited film of an inorganic oxide is formed on the stretched film surface of the ethylene-vinyl alcohol copolymer of the laminated stretched film obtained by performing a corona discharge treatment of about 100 w · min / m 2 Resin molded products.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6229676A JPH0892400A (en) | 1994-09-26 | 1994-09-26 | Surface treatment for thermoplastic resin sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6229676A JPH0892400A (en) | 1994-09-26 | 1994-09-26 | Surface treatment for thermoplastic resin sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0892400A true JPH0892400A (en) | 1996-04-09 |
Family
ID=16895947
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6229676A Pending JPH0892400A (en) | 1994-09-26 | 1994-09-26 | Surface treatment for thermoplastic resin sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0892400A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997047678A1 (en) * | 1996-06-12 | 1997-12-18 | Hoechst Trespaphan Gmbh | Method of priming polyolefin articles for coating |
US6086991A (en) * | 1996-06-12 | 2000-07-11 | Hoechst Trespaphan Gmbh | Method of priming poly(ethylene terephthalate) articles for coating |
US6254994B1 (en) | 1996-06-12 | 2001-07-03 | Hoechst Trespaphan Gmbh | Method of priming polyolefin articles for coating |
JP2001191460A (en) * | 1999-11-05 | 2001-07-17 | Tohcello Co Ltd | Laminate and method of manufacturing the same |
JP2002309022A (en) * | 2001-04-13 | 2002-10-23 | Mitsubishi Chemicals Corp | Method for producing gas barrier film |
JP2005290108A (en) * | 2004-03-31 | 2005-10-20 | Kuraray Co Ltd | Resin film for surface treatment and multilayered film using it |
KR100845365B1 (en) * | 2005-04-19 | 2008-07-10 | 세이코 엡슨 가부시키가이샤 | Electronic device substrate, liquid crystal panel, and electronic apparatus |
KR100845364B1 (en) * | 2005-04-19 | 2008-07-10 | 세이코 엡슨 가부시키가이샤 | Method of treating inorganic oxide film, electronic device substrate, method of manufacturing electronic device substrate, liquid crystal panel, and electronic apparatus |
JP2022009162A (en) * | 2019-09-30 | 2022-01-14 | 大日本印刷株式会社 | Barrier laminate, heat-sealable laminate having the barrier laminate, and packaging container having the heat-sealable laminate |
-
1994
- 1994-09-26 JP JP6229676A patent/JPH0892400A/en active Pending
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1086398C (en) * | 1996-06-12 | 2002-06-19 | 赫彻斯特-特拉丝帕番有限公司 | Method of priming polyolefin articles for coating |
US6086991A (en) * | 1996-06-12 | 2000-07-11 | Hoechst Trespaphan Gmbh | Method of priming poly(ethylene terephthalate) articles for coating |
AU733291B2 (en) * | 1996-06-12 | 2001-05-10 | Trespaphan Gmbh | Method of priming polyolefin articles for coating |
US6254994B1 (en) | 1996-06-12 | 2001-07-03 | Hoechst Trespaphan Gmbh | Method of priming polyolefin articles for coating |
US6368677B2 (en) * | 1996-06-12 | 2002-04-09 | Hoechst Trespaphan Gmbh | Method of priming polyolefin articles for coating |
WO1997047678A1 (en) * | 1996-06-12 | 1997-12-18 | Hoechst Trespaphan Gmbh | Method of priming polyolefin articles for coating |
JP2001191460A (en) * | 1999-11-05 | 2001-07-17 | Tohcello Co Ltd | Laminate and method of manufacturing the same |
JP2002309022A (en) * | 2001-04-13 | 2002-10-23 | Mitsubishi Chemicals Corp | Method for producing gas barrier film |
JP2005290108A (en) * | 2004-03-31 | 2005-10-20 | Kuraray Co Ltd | Resin film for surface treatment and multilayered film using it |
JP4593153B2 (en) * | 2004-03-31 | 2010-12-08 | 株式会社クラレ | Resin film for surface treatment and method for producing multilayer film using the same |
KR100845365B1 (en) * | 2005-04-19 | 2008-07-10 | 세이코 엡슨 가부시키가이샤 | Electronic device substrate, liquid crystal panel, and electronic apparatus |
KR100845364B1 (en) * | 2005-04-19 | 2008-07-10 | 세이코 엡슨 가부시키가이샤 | Method of treating inorganic oxide film, electronic device substrate, method of manufacturing electronic device substrate, liquid crystal panel, and electronic apparatus |
JP2022009162A (en) * | 2019-09-30 | 2022-01-14 | 大日本印刷株式会社 | Barrier laminate, heat-sealable laminate having the barrier laminate, and packaging container having the heat-sealable laminate |
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