JP2768616B2 - Heat shrinkable film for food packaging - Google Patents

Heat shrinkable film for food packaging

Info

Publication number
JP2768616B2
JP2768616B2 JP5034737A JP3473793A JP2768616B2 JP 2768616 B2 JP2768616 B2 JP 2768616B2 JP 5034737 A JP5034737 A JP 5034737A JP 3473793 A JP3473793 A JP 3473793A JP 2768616 B2 JP2768616 B2 JP 2768616B2
Authority
JP
Japan
Prior art keywords
film
ethylene
packaging
methacrylic acid
copolymer 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 - Lifetime
Application number
JP5034737A
Other languages
Japanese (ja)
Other versions
JPH06226926A (en
Inventor
賢郎 滝沢
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.)
Shin Etsu Polymer Co Ltd
Original Assignee
Shin Etsu Polymer 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 Shin Etsu Polymer Co Ltd filed Critical Shin Etsu Polymer Co Ltd
Priority to JP5034737A priority Critical patent/JP2768616B2/en
Publication of JPH06226926A publication Critical patent/JPH06226926A/en
Application granted granted Critical
Publication of JP2768616B2 publication Critical patent/JP2768616B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、食品または食品容器な
どの被包装物を包装するための食品包装用フィルムに関
するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a food packaging film for packaging a food or an object to be packaged such as a food container.

【0002】[0002]

【従来の技術】従来、青果物、鮮魚、精肉、惣菜等の食
品の包装やプラスチック等の軽量トレー上に食品を載せ
たものの包装、あるいは蓋付きの容器に食品を入れたも
のの包装等は、通常、フィルムでストレッチ包装により
行われている。ストレッチ包装とは、フィルムを伸ばし
た状態で被包装物を包装するものである。このようなフ
ィルムは、いわゆるプリパッケージ用フィルムと呼ば
れ、ポリ塩化ビニル樹脂(PVC)を素材としたフィル
ムが広く使われている。前記フィルムは、透明性と防曇
性があるので、水分の含む食品を包装しても曇ることな
く中身がよく見え、さらに自己粘着性があるので食品な
どを包装したあと、フィルムがバラけることがない。さ
らに弾性回復性があるのでフィルムを押したあと、シワ
や弛みなどが生じない特性がある。しかし、ポリ塩化ビ
ニル樹脂からなるフィルムは自動包装機械の適性や作業
適性等には優れている反面、近年、特に重要視されてい
る環境面あるいは安全衛生面で問題がある。このため、
上記フィルムの素材であるポリ塩化ビニル樹脂に代えて
環境面あるいは安全衛生面での問題の少ないポリオレフ
ィン系樹脂からなるフィルムが盛んに用いられている。
2. Description of the Related Art Conventionally, packaging of foods such as fruits and vegetables, fresh fish, meat, prepared foods, packaging of foods placed on lightweight trays of plastics, and packaging of foods in containers with lids, etc., are usually carried out. This is done by stretch wrapping with film. Stretch wrapping is to wrap an object to be wrapped with the film stretched. Such a film is called a so-called pre-packaging film, and a film made of a polyvinyl chloride resin (PVC) is widely used. The film has transparency and anti-fogging properties, so even when packaging food containing moisture, the contents can be seen well without fogging, and since it has self-adhesiveness, after packaging foods etc., the film may be loose. There is no. Furthermore, since it has elastic recovery properties, there is a characteristic that wrinkles and loosening do not occur after pressing the film. However, films made of polyvinyl chloride resin are excellent in suitability and workability of an automatic packaging machine, but have a problem in environmental or safety and hygiene, which has been particularly emphasized in recent years. For this reason,
In place of the polyvinyl chloride resin as a material of the above-mentioned film, a film made of a polyolefin-based resin having few problems on the environment or safety and health is widely used.

【0003】[0003]

【発明が解決しようとする課題】しかし、前記ポリオレ
フィン系樹脂フィルムは、環境および安全衛生面で問題
視されることは少ないが、上記したポリ塩化ビニル樹脂
に比べ、弾性回復力が劣るため、トレーに食品を載せた
トレーを包装した後にフィルムを手で押したりするとフ
ィルム表面にシワや弛みが発生し、綺麗な包装仕上がり
となりにくく商品価値を著しく低下させてしまうという
問題があった。
However, although the polyolefin resin film is rarely regarded as a problem in terms of the environment and health and safety, it is inferior in elastic recovery power to the polyvinyl chloride resin described above, so that the polyolefin resin film cannot be used. If the film is pressed by hand after packaging the tray on which the food is placed, the surface of the film is wrinkled or loosened, resulting in a problem that a beautiful package finish is hardly obtained and the commercial value is significantly reduced.

【0004】この欠点を解消するには、ポリオレフィン
系樹脂からなるフィルムに加熱収縮性を付与し、包装仕
上がりを向上させるために2軸延伸により延伸配向を行
うことによりフィルムにシュリンク性を持たせることが
考えられるが、加熱収縮性を得るには融点に近い温度で
ないと効果のないものが多く、また延伸配向が強くかか
っているため、フィルム自体の伸びが悪くフィルム幅に
対する被包装物の適応範囲が狭く、さらに強延伸のため
フィルムが配向しフィルムの方向性がはっきりして、フ
ィルムに一度穴が開くとそこから裂けが伝播し、収拾が
つかなくなるという問題があった。
In order to solve this drawback, it is necessary to impart heat shrinkage to a film made of a polyolefin resin, and to give the film a shrink property by performing biaxial stretching to improve the packaging finish. However, in order to obtain heat shrinkability, there are many things that are not effective unless the temperature is close to the melting point, and because the stretching orientation is strongly applied, the elongation of the film itself is poor and the applicable range of the packaged material to the film width However, the orientation of the film becomes clear due to the strong stretching, and the directionality of the film becomes clear, and once a hole is formed in the film, tears propagate from the hole, making it difficult to collect.

【0005】したがって、本発明は上記従来の問題点を
解決するもので、適度なシュリンク包装適性を有し、し
かもストレッチ包装適性をも兼ね備えた、包装の適用範
囲が広く、裂けに対する伝播の小さいポリオレフィン系
の食品包装用フィルム(以下、フィルムとする。)の提
供を課題とする。
Accordingly, the present invention solves the above-mentioned conventional problems, and has a suitable shrink wrapping suitability and also has a stretch wrapping suitability. An object of the present invention is to provide a system-based food packaging film (hereinafter, referred to as a film).

【0006】[0006]

【課題を解決するための手段】本発明者は、上記課題を
解決するため種々検討を重ねた結果、フィルムに不可欠
な特性である透明性、防曇性、自己粘着性、弾性回復性
をも有し、しかも上記課題を解決できる実用的に望まし
いポリオレフィン系のフィルムを開発した。
The present inventors have conducted various studies to solve the above-mentioned problems, and as a result, have found that the essential properties of the film are transparency, antifogging property, self-adhesiveness and elastic recovery. We have developed a practically desirable polyolefin-based film that has this and can solve the above problems.

【0007】すなわち、本発明は、メタクリル酸含有量
が8〜12重量%のエチレン−メタクリル酸共重合樹脂
を主成分とする中間層の両面に、酢酸ビニル含有量3.
5〜30重量%のエチレン−酢酸ビニル共重合体を主成
分とする樹脂層を設け、これをブロー比5以上でインフ
レーション成形してなる食品包装用熱収縮性フィルムを
要旨とするものである。
That is, according to the present invention, a vinyl acetate content of 3.about.12% by weight is contained on both surfaces of an intermediate layer mainly composed of an ethylene-methacrylic acid copolymer resin having a methacrylic acid content of 8 to 12% by weight.
A resin layer containing 5 to 30% by weight of an ethylene-vinyl acetate copolymer as a main component is provided.
SUMMARY OF THE INVENTION A heat-shrinkable film for food packaging formed by ration molding .

【0008】以下、本発明のフィルムについて詳細に説
明する。本発明のフィルムは、エチレン−メタクリル酸
共重合樹脂を主成分とする中間層と、その両面に積層さ
れるエチレン−酢酸ビニル共重合体を主成分とする樹脂
からなり、しかも各層中に含まれるメタクリル酸または
酢酸ビニルの含有量が特定の範囲内にあり、かつブロー
比5以上でインフレーション成形することに技術的な特
徴がある。
Hereinafter, the film of the present invention will be described in detail. The film of the present invention comprises an intermediate layer mainly composed of an ethylene-methacrylic acid copolymer resin and a resin mainly composed of an ethylene-vinyl acetate copolymer laminated on both surfaces thereof, and is contained in each layer. the content of methacrylic acid or vinyl acetate Ri certain range near and blow
There is a technical feature in inflation molding at a ratio of 5 or more .

【0009】まず、本発明のフィルムに用いられるエチ
レン−メタクリル酸共重合樹脂には、8〜12重量%の
メタクリル酸が含有される。このメタクリル酸含有量が
8重量%未満になるとフィルムの透明性および伸びが悪
くなるので好ましくなく、逆に12重量%を超えるとシ
ュリンク特性が発揮されず、包装したときにフィルムに
シワや弛みが発生するので好ましくない。また、このエ
チレン−メタクリル酸共重合樹脂には、必要に応じて所
望の添加剤等を配合して中間層としてもよい。
First, the ethylene-methacrylic acid copolymer resin used in the film of the present invention contains 8 to 12% by weight of methacrylic acid. When the methacrylic acid content is less than 8% by weight, the transparency and elongation of the film are deteriorated, which is not preferable. On the other hand, when the content exceeds 12% by weight, shrink properties are not exhibited, and when the film is wrapped, wrinkles or looseness occur. It is not preferable because it occurs. The ethylene-methacrylic acid copolymer resin may be mixed with a desired additive or the like as necessary to form an intermediate layer.

【0010】本発明のフィルムに用いられるエチレン−
酢酸ビニル共重合樹脂には、3.5〜30重量%の酢酸
ビニルが含有される。この酢酸ビニルの含有量が3.5
重量%未満の場合にはフィルムの透明性、伸び、自己粘
着性が悪くなるので好ましくなく、逆に30重量%を超
えるとフィルム同士のブロッキング現象が大きくなるた
め、フィルムとして巻き戻しにくくなるので好ましくな
い。このエチレン−酢酸ビニル共重合樹脂には、防曇
性、帯電防止性、適度の滑り性を付与することを目的と
してグリセリン脂肪酸エステル系、ソルビタン脂肪酸エ
ステル系、ポリグリセリン脂肪酸エステル系、エチレン
オキサイド付加物系の界面活性剤を添加することができ
る。また、上記エチレン−酢酸ビニル共重合樹脂に代え
てエチレン−エチルアクリレート共重合樹脂及びエチレ
ン−メチルメタクリレート共重合樹脂を用いてもよい。
The ethylene used in the film of the present invention
The vinyl acetate copolymer resin contains 3.5 to 30% by weight of vinyl acetate. When the content of this vinyl acetate is 3.5
When the content is less than 30% by weight, the transparency, elongation and self-adhesiveness of the film are deteriorated. On the other hand, when the content is more than 30% by weight, the blocking phenomenon between the films becomes large, and it becomes difficult to rewind the film. Absent. This ethylene-vinyl acetate copolymer resin has glycerin fatty acid ester type, sorbitan fatty acid ester type, polyglycerin fatty acid ester type, ethylene oxide adduct for the purpose of imparting antifogging property, antistatic property, and moderate slip property. A system surfactant can be added. Further, instead of the ethylene-vinyl acetate copolymer resin, an ethylene-ethyl acrylate copolymer resin and an ethylene-methyl methacrylate copolymer resin may be used.

【0011】本発明のフィルムを構成する中間層は、フ
ィルム全体層の厚さの30%以上であり、しかも中間層
の両面に積層されるエチレン−酢酸ビニル共重合樹脂層
の厚みが1μm以上であることが好ましい。中間層の厚
さが全体層の30%未満の場合には、延伸時のバブル安
定性が悪くなり、また上記樹脂層の厚みが1μm未満の
場合には、粘着性、透明性が発揮できないので好ましく
ない。
The thickness of the intermediate layer constituting the film of the present invention is at least 30% of the thickness of the entire film layer, and the thickness of the ethylene-vinyl acetate copolymer resin layer laminated on both surfaces of the intermediate layer is at least 1 μm. Preferably, there is. If the thickness of the intermediate layer is less than 30% of the entire layer, bubble stability during stretching is deteriorated, and if the thickness of the resin layer is less than 1 μm, adhesiveness and transparency cannot be exhibited. Not preferred.

【0012】上記のような構成のフィルムは、通常知ら
れている溶融共押出しインフレーション成形によりフィ
ルムに成形されるが、この時のブロー比は5以上でなけ
ればならない。このブローが5未満であると加熱収縮
性を付与することが困難であり、このためできるだけブ
ロー比を大きくして加熱収縮特性を付与することが望ま
しい。
[0012] The configuration of the film as described above, Fi by melt co-extrusion inflation molding commonly known
But the blow ratio at this time must be 5 or more.
I have to. If the blow ratio is less than 5, it is difficult to impart heat shrinkage. Therefore, it is desirable to increase the blow ratio as much as possible to impart heat shrink characteristics.

【0013】上記のように成形された本発明のフィルム
は、100℃における加熱収縮率が縦方向5%以上で、
横方向3%以上であり、120℃における加熱収縮率が
縦方向20%以上で、横方向20%以上であることが好
ましい。この100℃における加熱収縮率が縦方向5%
未満で、横方向3%未満である場合には、一般に食品の
包装工程上での高温加熱を嫌い、できるだけ低温度での
加熱収縮特性が求められているにもかかわらず、加熱収
縮時のフィルム温度を所定の温度まで上昇させないと収
縮が開始しないため、結果として高温加熱をしなければ
ならないという欠点があり、また所定の温度以下では加
熱収縮が不完全となり、シワなどが発生し包装仕上げが
綺麗にならないので好ましくない。また120℃におけ
る加熱収縮率が縦方向20%未満で、横方向20%未満
である場合には、加熱収縮後の包装仕上がりが綺麗に仕
上がらず、フィルムの張りが弱くシワや弛みの多く発生
するフィルムとなってしまうので好ましくない。
The film of the present invention formed as described above has a heat shrinkage at 100 ° C. of 5% or more in the machine direction,
It is preferably 3% or more in the horizontal direction, and the heat shrinkage at 120 ° C. is preferably 20% or more in the vertical direction and 20% or more in the horizontal direction. The heat shrinkage at 100 ° C. is 5% in the vertical direction.
If it is less than 3% in the transverse direction, it generally dislikes high-temperature heating in the packaging process of food, and although heat shrinkage properties at as low a temperature as possible are required, the film at the time of heat shrinkage Since the shrinkage does not start unless the temperature is raised to the predetermined temperature, there is a drawback that high-temperature heating must be performed as a result.At a temperature lower than the predetermined temperature, the heat shrinkage becomes incomplete, wrinkles are generated, and the packaging finish is finished. It is not preferable because it does not become clean. When the heat shrinkage rate at 120 ° C. is less than 20% in the vertical direction and less than 20% in the horizontal direction, the packaging finish after the heat shrinkage is not beautifully finished, the film is weak in tension, and many wrinkles and looseness are generated. It is not preferable because it becomes a film.

【0014】本発明のフィルムは、上記のような加熱収
縮率の範囲に加え、100%伸張時の応力が縦方向55
0Kgf/cm2 以下で、横方向350Kgf/cm2
以下であることが望ましい。この応力が縦方向550K
gf/cm2 を超え、横方向350Kgf/cm2 を超
えるとストレッチ包装を行う時に非常に大きな抵抗が起
こり、手で包装する際に腕や肩などに負担がかかる。ま
た自動包装機で包装する場合も包装物に対する機械の調
整幅が狭くなり、包装物のサイズ変更時ごとに機械調整
を行う必要が発生し、作業が繁雑になるので好ましくな
い。
In the film of the present invention, in addition to the above-mentioned range of the heat shrinkage, the stress at the time of 100% elongation is 55% in the longitudinal direction.
0 kgf / cm 2 or less, lateral 350 kgf / cm 2
It is desirable that: This stress is 550K in the vertical direction
If it exceeds gf / cm 2 and exceeds 350 kgf / cm 2 in the lateral direction, a very large resistance occurs when performing stretch packaging, and a burden is placed on the arms and shoulders when packing by hand. Also, in the case of packaging with an automatic packaging machine, the range of adjustment of the machine for the package is narrowed, and it is necessary to perform the machine adjustment every time the size of the package is changed, which is not preferable because the operation becomes complicated.

【0015】[0015]

【作用】本発明のフィルムは、加熱収縮特性がよく、機
械物性の優れたエチレン−メタクリル酸共重合樹脂を中
間層とし、その両面に透明性、自己粘着性等の優れたエ
チレン−酢酸ビニル共重合体の樹脂層を積層しているの
で、フィルム幅に対する被包装物の適応範囲が広く、裂
けに対する伝播も小さくした非PVC系フィルムが得ら
れる。
The film of the present invention has an intermediate layer of an ethylene-methacrylic acid copolymer resin having good heat shrinkage properties and excellent mechanical properties, and has an ethylene-vinyl acetate copolymer having excellent transparency and self-adhesiveness on both surfaces. Since the polymer resin layer is laminated, a non-PVC-based film having a wide range of applicability of the package to the film width and a small propagation to tear can be obtained.

【0016】[0016]

【実施例】【Example】

(実施例1)メタクリル酸含有量が9%のエチレン−メ
タクリル酸共重合樹脂を中間層とし、酢酸ビニル含有量
が19%のエチレン−酢酸共重合樹脂に界面活性剤を添
加した樹脂を中間層の両面に設け、ブロー条件を7、全
層の肉厚を10μm(中間層を7μm、それ以外を3μ
m)とし、インフレーション成形により、フィルムを製
造した。得られたフィルムの物性を下記に示す方法によ
り測定し、表1に示す結果を得た。表1から明らかなよ
うに、加熱収縮率、100%伸張時の応力は本発明を十
分満足し、フィルム成形性、自己粘着性、弾性回復力等
いずれも良好な結果が得られた。
(Example 1) An ethylene-methacrylic acid copolymer resin having a methacrylic acid content of 9% was used as an intermediate layer, and a resin obtained by adding a surfactant to an ethylene-acetic acid copolymer resin having a vinyl acetate content of 19% was used as an intermediate layer. And the thickness of all layers is 10 μm (7 μm for the intermediate layer, 3 μm for the other layers).
m), and a film was produced by inflation molding. The physical properties of the obtained film were measured by the following methods, and the results shown in Table 1 were obtained. As is clear from Table 1, the heat shrinkage and the stress at the time of 100% elongation sufficiently satisfied the present invention, and good results were obtained in all of the film formability, self-adhesiveness, and elastic recovery force.

【0017】(参考例1)実施例1において、エチレン
−酢酸共重合樹脂の代わりにエチレン−エチルアクリレ
ート共重合樹脂を用いて、実施例1と同様にフィルムを
製造した。得られたフィルムの物性を実施例1と同様に
下記に示す方法により測定し、表1に示す結果を得た。
表1から明らかなように、加熱収縮率、100%伸張時
の応力は本発明を十分満足し、フィルム成形性、自己粘
着性、弾性回復力等いずれも良好な結果が得られた。
Reference Example 1 A film was produced in the same manner as in Example 1 except that an ethylene-ethyl acrylate copolymer resin was used instead of the ethylene-acetic acid copolymer resin. The physical properties of the obtained film were measured by the following methods in the same manner as in Example 1, and the results shown in Table 1 were obtained.
As is clear from Table 1, the heat shrinkage and the stress at the time of 100% elongation sufficiently satisfied the present invention, and good results were obtained in all of the film formability, self-adhesiveness, and elastic recovery force.

【0018】(参考例2)実施例1において、エチレン
−酢酸共重合樹脂の代わりにエチレン−メチルメタクリ
レート共重合樹脂を用いて、実施例1と同様にフィルム
を製造した。得られたフィルムの物性を実施例1と同様
に下記に示す方法により測定し、表1に示す結果を得
た。表1から明らかなように、加熱収縮率、100%伸
張時の応力は本発明を十分満足し、フィルム成形性、自
己粘着性、弾性回復力等いずれも良好な結果が得られ
た。
Reference Example 2 A film was produced in the same manner as in Example 1 except that an ethylene-methyl methacrylate copolymer resin was used instead of the ethylene-acetic acid copolymer resin. The physical properties of the obtained film were measured by the following methods in the same manner as in Example 1, and the results shown in Table 1 were obtained. As is clear from Table 1, the heat shrinkage and the stress at the time of 100% elongation sufficiently satisfied the present invention, and good results were obtained in all of the film formability, self-adhesiveness, and elastic recovery force.

【0019】(比較例1)エチレン−メタクリル酸共重
合樹脂のメタクリル酸含有量を4%に変更し、それ以外
の条件を実施例1のままでフィルムを製造した。得られ
たフィルムの物性を実施例1と同様に下記に示す方法に
より測定し、表1に示す結果を得た。表1から明らかな
ように、加熱収縮率、100%伸張率の応力については
十分満足したが、Haze値が大きいため食品包装用として
の使用は困難であった。
Comparative Example 1 A film was produced in the same manner as in Example 1 except that the methacrylic acid content of the ethylene-methacrylic acid copolymer resin was changed to 4%. The physical properties of the obtained film were measured by the following methods in the same manner as in Example 1, and the results shown in Table 1 were obtained. As is evident from Table 1, the heat shrinkage and the stress at the 100% elongation were sufficiently satisfied, but the use of food packaging was difficult due to the large Haze value.

【0020】(比較例2)メタクリル酸含有量が4%の
エチレン−メタクリル酸共重合樹脂を中間層とし、酢酸
ビニル含有量が3%のエチレン−酢酸ビニル共重合樹脂
に界面活性剤を添加した樹脂を中間層の両面に設け、そ
れ以外の条件を実施例1のままでフィルムを製造した。
得られたフィルムの物性を実施例1と同様に下記に示す
方法により測定し、表1に示す結果を得た。表1から明
らかなように、加熱収縮率は十分満足したが、100%
伸張率時の応力が高く、Haze値も大きく、しかも自己粘
着性不足のため食品包装用としての使用は困難であっ
た。
Comparative Example 2 An ethylene-methacrylic acid copolymer resin having a methacrylic acid content of 4% was used as an intermediate layer, and a surfactant was added to an ethylene-vinyl acetate copolymer resin having a vinyl acetate content of 3%. A resin was provided on both surfaces of the intermediate layer, and a film was produced in the same manner as in Example 1 except for the above conditions.
The physical properties of the obtained film were measured by the following methods in the same manner as in Example 1, and the results shown in Table 1 were obtained. As is clear from Table 1, the heat shrinkage ratio was sufficiently satisfied, but was 100%.
It was difficult to use for food packaging due to high stress at elongation, high haze value, and lack of self-adhesion.

【0021】(比較例3)メタクリル酸含有量が13%
のエチレン−メタクリル酸共重合樹脂を中間層とし、酢
酸ビニル含有量が30%のエチレン−酢酸共重合樹脂に
界面活性剤を添加した樹脂を中間層の両面に設け、それ
以外の条件を実施例1のままでフィルムを製造した。得
られたフィルムの物性を実施例1と同様に下記に示す方
法により測定し、表1に示す結果を得た。表1から明ら
かなように、成形時のフィルム表面の粘着性が強すぎる
ため、フィルムを得ることができなかった。
(Comparative Example 3) The content of methacrylic acid is 13%
The ethylene-methacrylic acid copolymer resin of Example 1 was used as an intermediate layer, and a resin obtained by adding a surfactant to an ethylene-acetic acid copolymer resin having a vinyl acetate content of 30% was provided on both surfaces of the intermediate layer. A film was produced as it was. The physical properties of the obtained film were measured by the following methods in the same manner as in Example 1, and the results shown in Table 1 were obtained. As is clear from Table 1, the film could not be obtained because the adhesiveness of the film surface during molding was too strong.

【0022】[0022]

【表1】 [Table 1]

【0023】(物性評価) 1.透明性 フィルム一枚をJIS K−7105による試験方法で
測定し、Haze値を測定した。 2.防曇性 500ccビーカーに60℃のお湯を200cc入れた
後、ビーカー上面をフィルムで覆い、フィルムの曇りが
消える時間を測定する。 ○・・・10秒未満でフィルムの曇りが消える。 △・・・10秒以上でフィルムの曇りが消えるか、永久
に曇りが消えない。 3.自己粘着性 東洋精機製作所社製の「熱傾斜試験機」を使用し、フィ
ルムを重ねて二枚にしてテスト部にセットし、100
℃、1Kg/cm2 の圧力で、1秒間押える条件で試験
を行い、重ね部の溶着性が無理に剥離すると破れる程十
分に溶着しているのが良い。 ○・・・二枚のフィルムを剥そうとしてもなかなか剥れ
ない。 △・・・二枚のフィルムを剥すと容易に剥れる。 4.弾性回復力 茨木精機社製の自動包装機で包装を行い、包装物の中心
部に30gの球を10秒間乗せて外し、フィルムに残っ
たシワの取れるまでの時間を測定する。 ○・・・6秒未満でフィルムのシワが消える。 △・・・6秒以上かかってシワが消えるか、永久にシワ
が残ってしまう。 5.100%伸張率の応力 フィルム一枚をJIS K−6732に準ずる試験方法
で測定し、標線間が100%伸びた時の応力を測定す
る。 6.加熱収縮率 縦横共に10cmの正方形に切り取ったフィルムを10
0℃および120℃の温度のオーブンに1分間放置し、
取り出して縦横の長さを測定し、次式によって算出し
た。 加熱収縮率=(10−A)/100×100・・・% ただし、Aは取り出して測定した縦横の長さ 7.フィルムの伸び フィルム1枚をJIS K−6732に準ずる試験方法
で測定し、フィルム破断時の伸び率をフィルムの伸びと
して評価した。
(Evaluation of Physical Properties) Transparency One film was measured by the test method according to JIS K-7105, and the Haze value was measured. 2. Antifogging property After 200 cc of hot water at 60 ° C. is put into a 500 cc beaker, the upper surface of the beaker is covered with a film, and the time required for the film to be free from fogging is measured.・ ・ ・: Film fogging disappeared in less than 10 seconds. Δ: The fogging of the film disappeared after 10 seconds or more, or the fogging did not disappear forever. 3. Self-adhesiveness Using Toyo Seiki Seisakusho Co., Ltd.'s “Heat gradient tester”, superimpose two films and set them in the test section.
The test was carried out under the condition of pressing at 1 ° C./cm 2 at a pressure of 1 ° C. for 1 second, and it is preferable that the welded portion of the overlapped portion is sufficiently welded to be broken if it is forcibly peeled off.・ ・ ・: The two films are not easily peeled even when they are peeled. Δ: easily peels off when two films are peeled off. 4. Elastic recovery force Packaging is performed by an automatic packaging machine manufactured by Ibaraki Seiki Co., Ltd. A 30 g ball is placed on the center of the package for 10 seconds, removed, and the time until the wrinkles remaining on the film are removed is measured.・ ・ ・: Film wrinkles disappear in less than 6 seconds. Δ: Wrinkles disappear after 6 seconds or more, or wrinkles remain forever. 5. Stress at 100% Elongation Rate One film is measured by a test method according to JIS K-6732, and the stress when the interval between the marked lines is 100% is measured. 6. Heat shrinkage rate A film cut into a square of 10 cm in length and width is 10
Leave in an oven at 0 ° C and 120 ° C for 1 minute,
After being taken out, the length and length were measured and calculated by the following equation. Heat shrinkage rate = (10−A) / 100 × 100...% However, A is taken out and measured in length and width. Elongation of Film One film was measured by a test method according to JIS K-6732, and the elongation at break of the film was evaluated as the elongation of the film.

【0024】[0024]

【発明の効果】本発明のフィルムによれば、適度なシュ
リンク包装適性とストレッチ包装適性とを兼ね備えてい
るので、包装の適応範囲が広く、裂けに対する伝播の小
さい実用上きわめて望ましいポリオレフィン系のフィル
ムを提供することができる。
According to the film of the present invention, since it has both a suitable shrink wrapping suitability and a stretch wrapping suitability, a practically highly desirable polyolefin-based film having a wide application range of the wrapping and a small propagation to the tear is provided. Can be provided.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 メタクリル酸含有量が8〜12重量%の
エチレン−メタクリル酸共重合樹脂を主成分とする中間
層の両面に、酢酸ビニル含有量3.5〜30重量%のエ
チレン−酢酸ビニル共重合体を主成分とする樹脂を
け、これをブロー比5以上でインフレーション成形して
なることを特徴とする食品包装用熱収縮性フィルム。
1. An ethylene-vinyl acetate having a vinyl acetate content of 3.5 to 30% by weight is provided on both surfaces of an intermediate layer mainly containing an ethylene-methacrylic acid copolymer resin having a methacrylic acid content of 8 to 12% by weight. setting the resin composed mainly of a copolymer
A heat-shrinkable film for food packaging, wherein the heat-shrinkable film is formed by inflation molding with a blow ratio of 5 or more .
JP5034737A 1993-01-29 1993-01-29 Heat shrinkable film for food packaging Expired - Lifetime JP2768616B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5034737A JP2768616B2 (en) 1993-01-29 1993-01-29 Heat shrinkable film for food packaging

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5034737A JP2768616B2 (en) 1993-01-29 1993-01-29 Heat shrinkable film for food packaging

Publications (2)

Publication Number Publication Date
JPH06226926A JPH06226926A (en) 1994-08-16
JP2768616B2 true JP2768616B2 (en) 1998-06-25

Family

ID=12422637

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5034737A Expired - Lifetime JP2768616B2 (en) 1993-01-29 1993-01-29 Heat shrinkable film for food packaging

Country Status (1)

Country Link
JP (1) JP2768616B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6537178B2 (en) * 2015-08-07 2019-07-03 信越ポリマー株式会社 Method of manufacturing conductive stretched film

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07102652B2 (en) * 1992-03-05 1995-11-08 理研ビニル工業株式会社 Olefin wrap film

Also Published As

Publication number Publication date
JPH06226926A (en) 1994-08-16

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