JPH1036958A - Metal vapor deposited nylon film - Google Patents

Metal vapor deposited nylon film

Info

Publication number
JPH1036958A
JPH1036958A JP21199796A JP21199796A JPH1036958A JP H1036958 A JPH1036958 A JP H1036958A JP 21199796 A JP21199796 A JP 21199796A JP 21199796 A JP21199796 A JP 21199796A JP H1036958 A JPH1036958 A JP H1036958A
Authority
JP
Japan
Prior art keywords
metal
nylon film
deposited
metal vapor
vapor deposition
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.)
Granted
Application number
JP21199796A
Other languages
Japanese (ja)
Other versions
JP3451389B2 (en
Inventor
Shinya Kusama
震哉 草間
Masakazu Yamamoto
雅一 山本
Hideo Watanabe
英男 渡辺
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toyo Metallizing Co Ltd
Original Assignee
Toyo Metallizing Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyo Metallizing Co Ltd filed Critical Toyo Metallizing Co Ltd
Priority to JP21199796A priority Critical patent/JP3451389B2/en
Publication of JPH1036958A publication Critical patent/JPH1036958A/en
Application granted granted Critical
Publication of JP3451389B2 publication Critical patent/JP3451389B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Physical Vapour Deposition (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a metal vapor deposited nylon film excellent in adhesion for metal vapor deposition and usable in hot water without generating whitening after the coating of pressure sensitive adhesives or adhesives and interference film by successively forming a metal vapor deposition layer with nucleus and a metal vapor deposition layer under plasma discharge on an oriented nylon film. SOLUTION: As a preferable example, on the surface of an oriented nylon film having 12 to 25μm thickness, a metal vapor deposition layer of copper having 0.02 to 1.0nm average film thickness is formed under plasma discharge with 1 to 12kW/m strength in which the discharge gas is composed of oxygen, and on the surface, an Al metal vapor deposition layer having 10 to 100nm average film thickness is formed. This metal vapor deposition nylon film is the one in which the grain size of the metal vapor deposition layer is smaller than that free from metal vapor deposition with nucleus, and the falling resistance of the vapor deposition layers is improved.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は金属蒸着ナイロンフ
ィルムに関し、特に金属蒸着層の密着力の向上により耐
水性および耐熱水性を付与させたことを特徴とする金属
蒸着ナイロンフィルムに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a metal-deposited nylon film, and more particularly to a metal-deposited nylon film wherein water resistance and hot water resistance are imparted by improving the adhesion of a metal-deposited layer.

【0002】[0002]

【従来の技術】ナイロンフィルム上に金属蒸着したナイ
ロンフィルムは包装材料として広く使用されている。し
かし、ナイロンフィルム上に金属蒸着しただけではナイ
ロンフィルムと金属蒸着層間の密着力が不十分であっ
た。この密着力を向上させる方法として、ナイロンフィ
ルム上に予め樹脂からなるアンカ−コ−ト層を設け、そ
の上に金属蒸着を行う方法がすでに知られている。しか
し、この方法で得られる金属蒸着ナイロンフィルムは、
これに粘着剤あるいは接着剤をコ−トするとき、溶剤が
樹脂アンカ−コ−ト層を溶解して白化したり、あるいは
加熱乾燥による熱劣化により干渉膜を生じるという欠点
があった。さらに熱水により樹脂アンカ−コ−ト層を劣
化させ金属蒸着層の密着力が得られないという欠点があ
った。
2. Description of the Related Art Nylon films metal-deposited on nylon films are widely used as packaging materials. However, the adhesion between the nylon film and the metal-deposited layer was insufficient only by depositing the metal on the nylon film. As a method for improving the adhesion, there is already known a method in which an anchor coat layer made of a resin is previously provided on a nylon film, and a metal is vapor-deposited thereon. However, the metallized nylon film obtained by this method,
In this case, when the adhesive or the adhesive is coated, there is a disadvantage that the solvent dissolves the resin anchor coat layer to cause whitening, or an interference film is formed due to thermal deterioration due to heating and drying. Further, there is a disadvantage in that the resin anchor coat layer is deteriorated by the hot water and the adhesion of the metal deposition layer cannot be obtained.

【0003】また、金属蒸着層の密着力向上の処理方法
として単なる核付処理(特公昭52−25868号公
報)及び単なるプラズマ処理(特公平1−294875
号公報)なども知られているが、いずれの方法も性能と
して不十分であった。
Further, as a method of improving the adhesion of the metal deposition layer, a simple nucleation treatment (Japanese Patent Publication No. 52-25868) and a simple plasma treatment (Japanese Patent Publication No. 1-294875).
), But none of these methods has sufficient performance.

【0004】[0004]

【発明が解決しようとする課題】本発明は粘着剤あるい
は接着剤コ−ト後の白化、干渉膜の生じることなく、且
つ金属蒸着層の密着性に優れ、且つ熱水中で使用できる
金属蒸着ナイロンフィルムを提供することにある。
DISCLOSURE OF THE INVENTION The present invention provides a metal vapor deposition that can be used in hot water without causing whitening and interference film after coating of an adhesive or an adhesive, having excellent adhesion of a metal vapor deposited layer. An object of the present invention is to provide a nylon film.

【0005】[0005]

【課題を解決するための手段】本発明者らの鋭意検討の
結果、本発明の上記目的は下記の本発明により工業的に
有利に達成された。
As a result of intensive studies by the present inventors, the above object of the present invention has been industrially advantageously achieved by the following present invention.

【0006】[1]延伸ナイロンフィルム表面に、プラ
ズマ放電下による核付金属蒸着層、およびその上に金属
蒸着層をそれぞれ形成せしめてなる金属蒸着ナイロンフ
ィルム。
[1] A metal-deposited nylon film formed by forming a metal-deposited layer with a nucleus by plasma discharge on a surface of a stretched nylon film and a metal-deposited layer thereon.

【0007】[2]プラズマ放電の強度が1〜12kW
/mであることを特徴とする上記[1]記載の金属蒸着
ナイロンフィルム。
[2] Plasma discharge intensity of 1 to 12 kW
/ M, the metal-deposited nylon film according to the above [1].

【0008】[3]放電ガスが酸素であることを特徴と
する上記[1]もしくは上記[2]記載の金属蒸着ナイ
ロンフィルム。
[3] The metal-deposited nylon film according to the above [1] or [2], wherein the discharge gas is oxygen.

【0009】[4]プラズマ放電下による核付金属蒸着
層の金属が銅であることを特徴とする上記[1]〜
[3]記載の金属蒸着ナイロンフィルム。
[4] The above [1] to [1], wherein the metal of the nucleated metal deposition layer under plasma discharge is copper.
[3] The metal-deposited nylon film according to [3].

【0010】[5]金属蒸着層の金属がアルミニウムで
あることを特徴とする上記[1]〜[4]記載の金属蒸
着ナイロンフィルム。
[5] The metal-deposited nylon film according to the above [1] to [4], wherein the metal of the metal-deposited layer is aluminum.

【0011】[6]核付金属蒸着層の平均膜厚が0.0
2〜1.0nmであることを特徴とする上記[1]〜
[5]記載の金属蒸着ナイロンフィルム。
[6] The average film thickness of the cored metal deposition layer is 0.0
[1] to characterized in that the thickness is 2 to 1.0 nm.
[5] The metal-deposited nylon film according to [5].

【0012】[7]金属蒸着層の平均膜厚が10〜10
0nmであることを特徴とする上記[1]〜[6]記載
の金属蒸着ナイロンフィルム。
[7] The average thickness of the metal deposition layer is 10 to 10
The metal-deposited nylon film according to the above [1] to [6], which has a thickness of 0 nm.

【0013】[8]延伸ナイロンフィルムの厚みが12
〜25μmであることを特徴とする上記[1]〜[7]
記載の金属蒸着ナイロンフィルム。
[8] The stretched nylon film has a thickness of 12
[1] to [7], characterized in that the particle diameter is
The metal-deposited nylon film described in the above.

【0014】本発明の最大の特徴は延伸ナイロンフィル
ム表面に、プラズマ放電下に核付金属蒸着層、好ましく
は平均膜厚0.02〜1.0nmの核付金属蒸着層を形
成せしめ、その上に形成される好ましくは平均膜厚10
〜100nmの金属蒸着層とナイロンフィルムとの間の
密着力を向上せしめた点にある。
The most important feature of the present invention is that a nucleated metal deposition layer, preferably an average thickness of 0.02 to 1.0 nm, is formed on a stretched nylon film surface by plasma discharge. Preferably an average film thickness of 10
The point is that the adhesion between the metal deposited layer of about 100 nm and the nylon film is improved.

【0015】[0015]

【発明の実施の形態】次に本発明を詳しく説明する。Next, the present invention will be described in detail.

【0016】本発明において、ナイロンフィルムとして
は、特に制限はないが、6−ナイロンフィルム、6,6
−ナイロンフィルムが好ましい。その理由として、本発
明の目的は耐水性及び耐熱水性の付与にあり、この条件
に対応できるからであり、かつ安価に入手可能であるか
らである。本発明のナイロンフィルムの厚みは、包装材
料として使用する場合、12〜25μmの範囲であるこ
とが好ましい。また、ナイロンフィルムは、延伸されて
いることが必要である。
In the present invention, the nylon film is not particularly limited.
-Nylon films are preferred. The reason for this is that the object of the present invention is to provide water resistance and hot water resistance, which can cope with this condition, and that it is available at low cost. When used as a packaging material, the thickness of the nylon film of the present invention is preferably in the range of 12 to 25 μm. Further, the nylon film needs to be stretched.

【0017】蒸着されるフィルムは、非蒸着面に公知の
表面処理例えばコロナ放電処理、火炎処理、サンドマッ
ト加工およびヘア−ライン加工等の粗面化処理、あるい
は印刷が施されていても良い。
The film to be deposited may have been subjected to a known surface treatment, for example, a corona discharge treatment, a flame treatment, a roughening treatment such as a sand mat treatment and a hair-line treatment, or a printing on the non-deposited surface.

【0018】本発明におけるプラズマ放電下の核付金属
蒸着は、通常次のように行われる。
The nucleated metal deposition under the plasma discharge in the present invention is usually carried out as follows.

【0019】すなわち、酸素ガス雰囲気で、好ましくは
0.1〜100Paの雰囲気で、高周波電源より供給さ
れた電流をマグネトロン電極のカソ−ド及びアノ−ド間
で放電される。その際カソ−ドに核付金属蒸着層を構成
する銅を用いる。カソ−ドにガス陽イオンが引き寄せら
れ、カソ−ド金属をスパッタする。そのスパッタされた
金属がナイロンフィルムに付着し核付金属蒸着層を形成
する。プラズマ放電の処理強度は1〜12kW/mであ
ることが好ましい。この際放電処理強度が1kW/mよ
り小さい場合、フィルム上に付着するスパッタ金属は
0.1nm未満であり、且つフィルムに対するプラズマ
放電処理の表面処理効果は少なくなるので、処理強度が
1kW/m以上である事が好ましい。また、12kW/
mを越えた場合、ナイロンフィルム上の核付金属蒸着層
の厚みが1nmを越えてしまい、その金属色が確認でき
るようになり、外観上好ましくない。
That is, the current supplied from the high-frequency power supply is discharged between the cathode and the anode of the magnetron electrode in an oxygen gas atmosphere, preferably in an atmosphere of 0.1 to 100 Pa. At this time, copper constituting a metal deposition layer with a nucleus is used as a cathode. Gas cations are attracted to the cathode and sputter the cathode metal. The sputtered metal adheres to the nylon film to form a nucleated metal deposition layer. The processing intensity of the plasma discharge is preferably 1 to 12 kW / m. At this time, when the discharge treatment intensity is less than 1 kW / m, the amount of sputtered metal adhered on the film is less than 0.1 nm, and the surface treatment effect of the plasma discharge treatment on the film is reduced, so that the treatment intensity is 1 kW / m or more. It is preferred that In addition, 12kW /
If it exceeds m, the thickness of the nucleated metal deposition layer on the nylon film exceeds 1 nm, and its metal color can be confirmed, which is not preferable in appearance.

【0020】また、核付金属蒸着層上に蒸着する金属と
しては、特に制限はないが、スズ、クロム、銅及びアル
ミニウムが挙げられる。なかでも、色調及び蒸着適性か
らアルミニウムが最も好ましい。その蒸着方法は特に制
限されていないが、真空蒸着法、イオンプレ−ティング
法、スパッタリング法、イオンビ−ム法などが用いられ
る。この金属蒸着層の平均膜厚は通常10〜100nm
とする。
The metal deposited on the cored metal deposition layer is not particularly limited, but includes tin, chromium, copper and aluminum. Among them, aluminum is most preferable from the viewpoint of color tone and vapor deposition suitability. The vapor deposition method is not particularly limited, but a vacuum vapor deposition method, an ion plating method, a sputtering method, an ion beam method and the like are used. The average thickness of this metal deposition layer is usually 10 to 100 nm.
And

【0021】[0021]

【実施例】以下、本発明を実施例により、更に詳細に説
明するが、本発明は、これらに限定されるものではな
い。
EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited thereto.

【0022】なお、実施例及び比較例中の物性は次によ
うにして測定した。
The physical properties in Examples and Comparative Examples were measured as follows.

【0023】(1)酸素透過率 ASTM D−3985に準じて、酸素透過率測定装置
(モダンコントロ−ル社製OX−TRAN100)を用
いて20℃、0%RHの条件で測定した。
(1) Oxygen Permeability According to ASTM D-3985, oxygen permeability was measured at 20 ° C. and 0% RH using an oxygen permeability measuring device (OX-TRAN100 manufactured by Modern Control Co., Ltd.).

【0024】(2)ラミネ−ト強度 蒸着面にウレタン系2液型接着剤をドライで2μm相当
をコ−トし、60μmの未延伸PPフィルムとラミネ−
トし、18時間、40℃雰囲気でエ−ジングする。その
後、15mm幅×200mm長に切り取り、オリエンテ
ック社製テンシロン万能試験機を用いて引張速度200
mm/min.で90°剥離時の未チャック強度として
評価した。(ドライラミネート強度)また、90°剥離
時剥離界面に蒸留水を2〜3滴滴下して、同様に密着強
度を評価した。(ウェットラミネ−ト強度)蒸着フィル
ムサンプルの調整方法は次の通りである。
(2) Laminate strength A urethane-based two-component adhesive was dry-coated to a thickness of 2 μm on the surface to be vapor-deposited, and an unstretched PP film of 60 μm and a laminate were coated.
And aged at 40 ° C. for 18 hours. After that, it was cut into 15 mm width × 200 mm length, and the tensile speed was set to 200 using an Orientec Tensilon universal testing machine.
mm / min. Was evaluated as the non-chuck strength at 90 ° peeling. (Dry Lamination Strength) Further, 2-3 drops of distilled water were dropped on the peeling interface at the time of peeling at 90 °, and the adhesion strength was evaluated in the same manner. (Wet Laminate Strength) The method of preparing a vapor-deposited film sample is as follows.

【0025】(1)ボイル処理 蒸着フィルムの蒸着面にウレタン2液型接着剤を固型分
2μm厚相当をコ−トし、60μmの未延伸PPフィル
ムとラミネ−トし、40℃で72時間エージングする。
エ−ジング後ラミネ−トフィルムを12cm角にカット
する。60μmの未延伸PPフィルムを内側になるよう
に2枚重ね、三方シ−ルする。袋状になったところに蒸
留水を100ml入れ、さらに空気が入らないようにし
て開放部分をシ−ルし、密封状態にする。このサンプル
を95℃の沸騰水中に30分間放置し、その後取り出し
てシ−ル部をカットし、水蒸気透過率、酸素透過率の測
定用サンプルとした。
(1) Boil treatment A two-part urethane adhesive is coated on the vapor-deposited surface of the vapor-deposited film in an amount equivalent to a thickness of 2 μm for a solid part. Aging.
After aging, the laminate film is cut into 12 cm square. Two unstretched PP films each having a thickness of 60 μm are overlapped so as to face the inside, and three-way sealing is performed. 100 ml of distilled water is put into the bag-shaped portion, and the open portion is sealed so as not to allow air to enter, and the bag is sealed. This sample was allowed to stand in boiling water at 95 ° C. for 30 minutes, and then taken out and cut off the seal portion to obtain a sample for measuring water vapor transmission rate and oxygen transmission rate.

【0026】[実施例1]〜[実施例4]、[比較例
1]〜[比較例6] プラスチックフィルムとして厚さ15μm、1000m
m幅の二軸延伸ナイロンフィルムを用いて通常のロ−ル
・ツ−・ロ−ル型の蒸着機で1×10-3mmHgの真空
下でマグネトロン電極のカソ−ドに純度99.9%の銅
材を用いて酸素0.5l/min.を放電雰囲気で供給
する。更に、マグネトロン電極に電圧をかけ放電電流の
プラズマ放電雰囲気でナイロンフィルム上にそれぞれ次
に示す平均厚みの核付金属蒸着層を形成した。引き続き
1×10-4mmHgの真空下でアルミ蒸着層を40nm
形成させた。
[Example 1] to [Example 4], [Comparative Example 1] to [Comparative Example 6] A plastic film having a thickness of 15 μm and a thickness of 1000 m
Using a biaxially stretched nylon film having a width of m and a roll-to-roll type evaporator under a vacuum of 1 × 10 -3 mmHg, the purity of the magnetron electrode was 99.9%. 0.5 l / min. Is supplied in a discharge atmosphere. Further, a voltage was applied to the magnetron electrode, and a nucleated metal deposition layer having the following average thickness was formed on the nylon film in a plasma discharge atmosphere of a discharge current. Then, under vacuum of 1 × 10 −4 mmHg, the aluminum deposition layer is
Formed.

【0027】 実施例1:0.01nm 実施例2:0.1nm 実施例3:1.0nm 実施例4:2.0nm 一方、比較例1は核付金属蒸着層を形成することなく4
0nmのアルミニウム蒸着層を形成させた。また、比較
例2ではコロナ放電処理面に同様の蒸着層を形成させ
た。比較例3は核付蒸着層を形成させずナイロンフィル
ムをプラズマ放電雰囲気中に通し、引き続き40nmの
アルミニウム蒸着層を形成させた。比較例4では抵抗加
熱方式で銅を1.0nmの厚みで核付金属蒸着層を形成
し、引き続いて40nmのアルミニウム蒸着層を形成さ
せた。比較例5では放電ガスである酸素ガスの代わりに
窒素ガスを用いて1.0nmの核付金属蒸着層を形成さ
せ、引き続いて40nmのアルミニウム蒸着層を形成さ
せた。また、比較例6では放電ガスである酸素ガスの代
わりにアルゴンガスを用いて1.0nmの核付金属蒸着
層を形成させ、引き続いて40nmのアルミニウム蒸着
層を形成させた。
Example 1: 0.01 nm Example 2: 0.1 nm Example 3: 1.0 nm Example 4: 2.0 nm On the other hand, Comparative Example 1 shows 4 without forming a cored metal deposition layer.
An aluminum deposited layer of 0 nm was formed. In Comparative Example 2, a similar vapor deposition layer was formed on the corona discharge treated surface. In Comparative Example 3, a nylon film was passed through a plasma discharge atmosphere without forming a nucleated vapor deposition layer, and a 40 nm aluminum vapor deposition layer was subsequently formed. In Comparative Example 4, a nucleated metal vapor-deposited layer of copper was formed to a thickness of 1.0 nm by a resistance heating method, and subsequently a 40 nm-thick aluminum vapor-deposited layer was formed. In Comparative Example 5, a 1.0-nm nucleated metal vapor-deposited layer was formed using nitrogen gas instead of oxygen gas as a discharge gas, and subsequently a 40-nm aluminum vapor-deposited layer was formed. In Comparative Example 6, a 1.0-nm nucleated metal vapor-deposited layer was formed using argon gas instead of oxygen gas as a discharge gas, and subsequently a 40-nm aluminum vapor-deposited layer was formed.

【0028】表1に実施例1〜4と比較例1〜6の特性
の測定結果をまとめた。
Table 1 summarizes the measurement results of the characteristics of Examples 1 to 4 and Comparative Examples 1 to 6.

【0029】[0029]

【表1】 表1から明らかなように、実施例1〜4により得られた
金属蒸着フィルムは、ガスバリア−性(未処理、ボイル
処理)がいずれの処理を比較しても比較例1〜6よりレ
ベルアップし且つラミネ−ト強度(耐水密着性)につい
ても同様の結果が得られた。
[Table 1] As is clear from Table 1, the metal vapor-deposited films obtained in Examples 1 to 4 have higher gas barrier properties (untreated, boiled) than those of Comparative Examples 1 to 6 regardless of the treatment. The same result was obtained for the laminate strength (water resistance).

【0030】[0030]

【発明の効果】本発明では、プラスチックフィルム上に
特定の核付金属蒸着層及び金属蒸着層を順次形成するこ
とにより、金属蒸着層のグレインサイズが核付蒸着層の
ないものに比べて小さく且つ蒸着層の脱落が改良された
ナイロンフィルムとなる。したがって、本発明はラミネ
−ト強度の必要な食品包装用蒸着フィルムに特に有効で
ある。
According to the present invention, by sequentially forming a specific nucleated metal deposition layer and a metal deposition layer on a plastic film, the grain size of the metal deposition layer is smaller than that without the nucleation deposition layer. The resulting nylon film has an improved removal of the deposited layer. Therefore, the present invention is particularly effective for a vapor-deposited film for food packaging requiring a laminate strength.

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】延伸ナイロンフィルム表面に、プラズマ放
電下による核付金属蒸着層、およびその上に金属蒸着層
をそれぞれ形成せしめてなる金属蒸着ナイロンフィル
ム。
1. A metal-deposited nylon film formed by forming a metal-deposited layer with a nucleus by plasma discharge on a surface of a stretched nylon film and a metal-deposited layer thereon.
【請求項2】プラズマ放電の強度が1〜12kW/mで
あることを特徴とする請求項1記載の金属蒸着ナイロン
フィルム。
2. The metal-deposited nylon film according to claim 1, wherein the intensity of the plasma discharge is 1 to 12 kW / m.
【請求項3】放電ガスが酸素であることを特徴とする請
求項1もしくは請求項2記載の金属蒸着ナイロンフィル
ム。
3. The metal-deposited nylon film according to claim 1, wherein the discharge gas is oxygen.
【請求項4】プラズマ放電下による核付金属蒸着層の金
属が、銅であることを特徴とする請求項1〜3記載のい
ずれかに記載の金属蒸着ナイロンフィルム。
4. The metal-deposited nylon film according to claim 1, wherein the metal of the metal-deposited nucleation layer under plasma discharge is copper.
【請求項5】金属蒸着層の金属がアルミニウムであるこ
とを特徴とする請求項1〜4のいずれかに記載の金属蒸
着ナイロンフィルム。
5. The metal-deposited nylon film according to claim 1, wherein the metal of the metal-deposited layer is aluminum.
【請求項6】核付金属の平均膜厚が0.02〜1.0n
mであることを特徴とする請求項1〜5のいずれかに記
載の金属蒸着ナイロンフィルム。
6. The cored metal has an average thickness of 0.02 to 1.0 n.
The metal-deposited nylon film according to any one of claims 1 to 5, wherein m is m.
【請求項7】金属蒸着層の平均膜厚が10〜100nm
であることを特徴とする請求項1〜6のいずれかに記載
の金属蒸着ナイロンフィルム。
7. The metal deposited layer has an average thickness of 10 to 100 nm.
The metallized nylon film according to any one of claims 1 to 6, wherein
【請求項8】延伸ナイロンフィルムの厚みが12〜25
μmであることを特徴とする請求項1〜7のいずれかに
記載の金属蒸着ナイロンフィルム。
8. The stretched nylon film has a thickness of 12 to 25.
The metal-deposited nylon film according to any one of claims 1 to 7, wherein the thickness is μm.
JP21199796A 1996-07-23 1996-07-23 Manufacturing method of metallized nylon film Expired - Fee Related JP3451389B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21199796A JP3451389B2 (en) 1996-07-23 1996-07-23 Manufacturing method of metallized nylon film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21199796A JP3451389B2 (en) 1996-07-23 1996-07-23 Manufacturing method of metallized nylon film

Publications (2)

Publication Number Publication Date
JPH1036958A true JPH1036958A (en) 1998-02-10
JP3451389B2 JP3451389B2 (en) 2003-09-29

Family

ID=16615191

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21199796A Expired - Fee Related JP3451389B2 (en) 1996-07-23 1996-07-23 Manufacturing method of metallized nylon film

Country Status (1)

Country Link
JP (1) JP3451389B2 (en)

Also Published As

Publication number Publication date
JP3451389B2 (en) 2003-09-29

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