JPH0337505B2 - - Google Patents
Info
- Publication number
- JPH0337505B2 JPH0337505B2 JP20544983A JP20544983A JPH0337505B2 JP H0337505 B2 JPH0337505 B2 JP H0337505B2 JP 20544983 A JP20544983 A JP 20544983A JP 20544983 A JP20544983 A JP 20544983A JP H0337505 B2 JPH0337505 B2 JP H0337505B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- nylon
- thickness
- composite film
- polyamide resin
- 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.)
- Expired
Links
Landscapes
- Laminated Bodies (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Description
本発明は、スライスハム等の食品の包装に適
し、特に外観の優れた深絞り成形用複合フイルム
に関する。
スライスハム等を包装するための深絞り成形用
複合フイルムとしては、耐ピンホール性を付与す
るポリアミド樹脂層及び蓋材とのヒートシール性
を付与するシール性樹脂層を必須の構成要素と
し、好ましくはガスバリアー性樹脂層を有する各
種構成のものが一般に使用されている。
深絞り成形用複合フイルムの重要な品質の一つ
として、深絞り成形後の成形品の天部にしわ入り
等がない外観の優れたものが要求される。従来、
上記構成のもので成形品の天部にしわ入り等がな
い外観上満足できるものはなかつた。
本発明者は成形品の天部に発生するしわ入り等
の原因につき、種々検討した結果、複合フイルム
を構成する樹脂の一つであるポリアミド樹脂が最
も関与していることが判つた。そこで、通常ポリ
アミド樹脂として使用されている6ナイロン、66
ナイロン、6−66ナイロン等からなるポリアミド
樹脂層の肉厚をできるかぎり薄くし影響を少なく
することを検討したが、薄くすることによつて耐
ピンホール性が低下し、成形条件によつてはピン
ホールが発生し易いという欠点がある。
本発明は、特定の組成からなる共重合ポリアミ
ド樹脂を使用することによつて、ポリアミド樹脂
層の肉厚を薄くすることなく、外観を向上させた
ものである。
本発明に使用する共重合ポリアミド樹脂は、6
ナイロンを主体とし、他成分をヘキサメチレンジ
アミンとテレフタル酸との重縮合物としたもの
(以下「6−6Tナイロン」という。)又は同様に
6ナイロンを主体とし、他成分をヘキサメチレン
ジアミンとイソフタル酸との重縮合物としたもの
(以下「6−6Iナイロン」という。)である。また
上記両酸を併用したものでもよい。上記共重合ポ
リアミド樹脂の組成比率は、両者とも6ナイロ
ン、95〜80重量%に対し、他成分の6Tナイロン
又は6Iナイロンあるいはそれらの混合物を5〜20
重量%の範囲とすることが好ましく、他成分が5
重量%未満のものは外観改良の効果が見られず、
また他成分が20重量を越すものについては共重合
体の製造が困難な為不都合である。
本発明の複合フイルムにおけるポリアミド樹脂
層以外の層構成については、各種樹脂の使用や組
合せが可能である。
シール性樹脂としてはアイオノマー樹脂、ポリ
エチレン、エチレンと他の成分との共重合体が好
適に使用でき、またガスバリアー性樹脂層として
は、エチレン−酢酸ビニル共重合体けん化物等が
使用できる。更に層間の接着強度を向上させる目
的で変性ポリオレフイン等の接着性樹脂を介在さ
せてもよい。
本発明の複合フイルムの製造方法については、
各樹脂層を共押出し法により積層する方法が得ら
れるフイルムの特性や生産性の点から好ましい。
以下本発明を実施例にて説明する。
実施例
後述する各構成の複合フイルムを第1層が外側
になるよう、三菱重工(株)製の深絞り成形機MVP
−401型で100℃×2秒間加熱した後、3.0Kg/cm2
のゲージ圧力で直径100mm深さ30mmの大きさに絞
り成形した。ただちに成形加工した孔の中に直径
98mmのスライスハム200gを充填し、下記の蓋材
を被せて真空包装した後、160mm×130mmの矩形に
裁断して各包装体とした。得られた各包装体を1
週間放置(5℃、100%相対湿度の雰囲気中)後
の外観(天部のしわ等)及び耐ピンホール性の評
価結果を表−1に示す。なお天部のしわについて
は、深絞り成形時の加熱条件を90℃×2秒間とし
たものについても評価した。蓋材としては、無延
伸のポリプロピレン(厚さ20μ)/塩化ビニリデ
ンをコートしたセロフアン(30μ)/アイオノマ
ー樹脂(30μ)からなるフイルムを使用した。外
観の評価については、肉眼観察し、該当の欠点が
全くなく極めて優れているもの(◎)、欠点がほ
とんどなく良好なもの(〇)、欠点が見られる問
題のあるもの(△)とした。
耐ピンホール性の評価は、上述した成形条件に
おいて、深さの異なる2種の金型を用いて絞り成
形を行ない評価した。深さ40mmまでピンホールの
生じないもの(◎)、深さ30mmまでピンホールの
生じないもの(〇)とした。
発明品1
第1層(外側層)のガスバリアー性樹脂層にエ
チレン含有率45モル%、けん化度99.5モル%のエ
チレン−酢酸ビニル共重合体けん化物、第2層の
ポリアミド樹脂層として6Tナイロンの含率が10
重量%の6−6Tナイロンを、第3層として変性
ポリオレフイン(アドマ−LF−305、三井石油化
学工業(株)製)を、第4層のシール性樹脂層とし
て、酢酸ビニル含有率5%のエチレン−酢酸ビニ
ル共重合体の構成となるように、各樹脂を設定温
度230℃の共押出し環状口金内で積層した後、冷
却して直径270mmのインフレーシヨンフイルムを
得た。各層の厚さ構成は、第1層が30μ、第2層
が10μ、第3層が15μ、第4層が95μである。
発明品2
発明品1と同一の材料を使用し、厚さ構成の異
なる複合フイルムを得た。第1層が30μ、第2層
が30μ、第3層が15μ、第4層が75μである。
発明品3
第2層のポリアミド樹脂層として、6Iナイロン
の含有率が10重量%の6−6Iナイロンを使用した
他は発明品1と同じ材料を使用した複合フイル
ム。第1層が30μ、第2層が10μ、第3層が15μ、
第4層が95μである。
発明品4
発明品3と同一の材料を使用し、厚さ構成の異
なる複合フイルムを得た。第1層が30μ、第2層
が30μ、第3層が15μ、第4層が75μである。
比較品1
第2層のポリアミド樹脂層として66ナイロンの
含有率が15重量%の6−66ナイロンを使用した他
は発明品1と同じ材料を使用した複合フイルム。
第1層が30μ、第2層が10μ、第3層が15μ、第4
層が95μである。
比較品2
比較品1と同一の材料を使用し、厚さ構成の異
なる複合フイルム。第1層が30μ、第2層が30μ、
第3層が15μ、第4層が75μである。
The present invention relates to a composite film for deep drawing, which is suitable for packaging foods such as sliced ham, and particularly has an excellent appearance. A composite film for deep drawing for packaging sliced ham etc. preferably includes a polyamide resin layer that provides pinhole resistance and a sealing resin layer that provides heat sealability with the lid material. Various structures having a gas barrier resin layer are generally used. One of the important qualities of a composite film for deep drawing is that it has an excellent appearance without wrinkles on the top of the molded product after deep drawing. Conventionally,
None of the molded products having the above structure had a satisfactory appearance without wrinkles on the top of the molded product. The inventors of the present invention have conducted various studies on the causes of wrinkles occurring on the top of molded products, and have found that polyamide resin, one of the resins constituting the composite film, is most responsible. Therefore, nylon 6, which is usually used as polyamide resin,
We considered reducing the thickness of the polyamide resin layer made of nylon, 6-66 nylon, etc. to reduce the effect as much as possible, but by making it thinner, the pinhole resistance deteriorates, and depending on the molding conditions, It has the disadvantage that pinholes are likely to occur. The present invention improves the appearance without reducing the thickness of the polyamide resin layer by using a copolyamide resin having a specific composition. The copolyamide resin used in the present invention is 6
A polycondensate of hexamethylene diamine and terephthalic acid with nylon as the main component (hereinafter referred to as "6-6T nylon"); It is a polycondensate with an acid (hereinafter referred to as "6-6I nylon"). Further, a combination of both of the above acids may be used. The composition ratio of the copolymerized polyamide resin is 95 to 80% by weight of 6 nylon, and 5 to 20% by weight of 6T nylon, 6I nylon, or a mixture thereof.
It is preferable that the other components are in the range of 5% by weight.
If it is less than % by weight, no effect of appearance improvement can be seen.
Moreover, if the weight of other components exceeds 20, it is difficult to produce a copolymer, which is disadvantageous. Regarding the layer structure other than the polyamide resin layer in the composite film of the present invention, various resins can be used or combined. Ionomer resins, polyethylene, and copolymers of ethylene and other components can be suitably used as the sealing resin, and saponified ethylene-vinyl acetate copolymers can be used as the gas barrier resin layer. Furthermore, adhesive resin such as modified polyolefin may be interposed for the purpose of improving the adhesive strength between the layers. Regarding the method for manufacturing the composite film of the present invention,
A method in which each resin layer is laminated by coextrusion is preferred from the viewpoint of the properties and productivity of the resulting film. The present invention will be explained below with reference to Examples. Example: Composite films with each configuration described below were processed using a deep drawing machine MVP manufactured by Mitsubishi Heavy Industries, Ltd. so that the first layer was on the outside.
-3.0Kg/cm 2 after heating at 100℃ for 2 seconds with type 401
It was drawn to a size of 100 mm in diameter and 30 mm in depth using a gauge pressure of . diameter into the hole that is immediately formed.
Each package was filled with 200 g of 98 mm sliced ham, covered with the following lid material, vacuum packaged, and then cut into a 160 mm x 130 mm rectangle. 1 of each package obtained
Table 1 shows the evaluation results of the appearance (wrinkles on the top, etc.) and pinhole resistance after being left for a week (in an atmosphere of 5° C. and 100% relative humidity). Regarding the wrinkles on the top, the heating conditions during deep drawing were also evaluated at 90°C for 2 seconds. As the lid material, a film consisting of unstretched polypropylene (thickness 20μ)/cellophane coated with vinylidene chloride (30μ)/ionomer resin (30μ) was used. The appearance was evaluated by visual observation and was rated as excellent (◎) with no defects, good (◎) with almost no defects, and problematic (△) with visible defects. The pinhole resistance was evaluated by performing draw forming under the above-mentioned forming conditions using two types of molds with different depths. Items with no pinholes up to a depth of 40 mm (◎) and items with no pinholes up to a depth of 30 mm (○) were rated. Invention Product 1 The first gas barrier resin layer (outer layer) is a saponified ethylene-vinyl acetate copolymer with an ethylene content of 45 mol% and a saponification degree of 99.5 mol%, and the second polyamide resin layer is 6T nylon. The content of is 10
% by weight of 6-6T nylon, the third layer was modified polyolefin (ADMER-LF-305, manufactured by Mitsui Petrochemical Industries, Ltd.), and the fourth layer was a sealing resin layer with a vinyl acetate content of 5%. Each resin was laminated in a coextrusion annular die at a set temperature of 230° C. to form an ethylene-vinyl acetate copolymer, and then cooled to obtain a blown film with a diameter of 270 mm. The thickness of each layer is 30μ for the first layer, 10μ for the second layer, 15μ for the third layer, and 95μ for the fourth layer. Invention Product 2 Using the same material as Invention Product 1, a composite film with a different thickness structure was obtained. The first layer has a thickness of 30μ, the second layer has a thickness of 30μ, the third layer has a thickness of 15μ, and the fourth layer has a thickness of 75μ. Invention Product 3 A composite film using the same materials as Invention Product 1, except that 6-6I nylon with a 6I nylon content of 10% by weight was used as the second polyamide resin layer. The first layer is 30μ, the second layer is 10μ, the third layer is 15μ,
The fourth layer is 95μ. Invention Product 4 Using the same material as Invention Product 3, a composite film with a different thickness structure was obtained. The first layer has a thickness of 30μ, the second layer has a thickness of 30μ, the third layer has a thickness of 15μ, and the fourth layer has a thickness of 75μ. Comparative Product 1 A composite film using the same materials as Invention Product 1, except that 6-66 nylon with a 66 nylon content of 15% by weight was used as the second polyamide resin layer.
1st layer 30μ, 2nd layer 10μ, 3rd layer 15μ, 4th layer
The layer is 95μ. Comparison product 2 Composite film using the same material as comparison product 1 but with a different thickness structure. The first layer is 30μ, the second layer is 30μ,
The thickness of the third layer is 15μ, and the thickness of the fourth layer is 75μ.
【表】【table】
【表】
表−1から本発明品1〜4に比較し、発明品と
ポリアミド樹脂層の使用樹脂が異なる比較品1、
2では外観が劣り、成形条件が低温のもの(90℃
×2秒間)では天部のしわ入りが発生することが
判る。
特に肉厚の厚い比較品2では外観が悪くなるこ
とが判る。これに対し、本発明品は肉厚が厚い
(発明品2、4)のものでも外観が優れ、成形条
件が低温でも天部のしわ入りが発生しないことが
判る。
上述したように、本発明は、食品包装に適した
深絞り成形用複合フイルムを提供するものであ
り、その効果は著しく大きい。[Table] From Table-1, compared to the invention products 1 to 4, comparative product 1, which uses a different resin for the polyamide resin layer,
In No. 2, the appearance is inferior and the molding conditions are low (90℃).
x 2 seconds), it can be seen that wrinkles appear on the top. In particular, it can be seen that the comparative product 2, which has a thick wall, has a poor appearance. On the other hand, it can be seen that the products of the present invention, even those with thick walls (Invention Products 2 and 4), have an excellent appearance, and wrinkles do not occur at the top even under low temperature molding conditions. As described above, the present invention provides a composite film for deep drawing that is suitable for food packaging, and its effects are significantly large.
Claims (1)
脂層を有する深絞り成形用複合フイルムにおい
て、上記ポリアミド樹脂層が6ナイロンを主体と
し、他成分をヘキサメチレンジアミンとテレフタ
ル酸及び又はイソフタル酸との重縮合物とした共
重合ポリアミド樹脂からなることを特徴とする深
絞り成形用複合フイルム。1. In a composite film for deep drawing having at least a polyamide resin layer and a sealing resin layer, the polyamide resin layer is mainly composed of nylon 6, and other components are a polycondensate of hexamethylene diamine and terephthalic acid and/or isophthalic acid. A composite film for deep drawing, characterized by being made of a copolymerized polyamide resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20544983A JPS6097850A (en) | 1983-11-01 | 1983-11-01 | Composite film for deep-drawing molding |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20544983A JPS6097850A (en) | 1983-11-01 | 1983-11-01 | Composite film for deep-drawing molding |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6097850A JPS6097850A (en) | 1985-05-31 |
| JPH0337505B2 true JPH0337505B2 (en) | 1991-06-05 |
Family
ID=16507060
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20544983A Granted JPS6097850A (en) | 1983-11-01 | 1983-11-01 | Composite film for deep-drawing molding |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6097850A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62227626A (en) * | 1986-03-31 | 1987-10-06 | Kohjin Co Ltd | Shrinkable polyamide film and manufacture thereof |
| US4800129A (en) * | 1987-03-26 | 1989-01-24 | E. I. Du Pont De Nemours And Company | Multi-layer plastic container |
| JPH069916B2 (en) * | 1987-12-11 | 1994-02-09 | 三井・デュポンポリケミカル株式会社 | Coextrusion composite film |
| EP0755778A1 (en) | 1995-07-28 | 1997-01-29 | Wolff Walsrode Ag | Sterilisable barrier film based on polyamides and polyolefins |
-
1983
- 1983-11-01 JP JP20544983A patent/JPS6097850A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6097850A (en) | 1985-05-31 |
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