JPS6253011B2 - - Google Patents

Info

Publication number
JPS6253011B2
JPS6253011B2 JP57110084A JP11008482A JPS6253011B2 JP S6253011 B2 JPS6253011 B2 JP S6253011B2 JP 57110084 A JP57110084 A JP 57110084A JP 11008482 A JP11008482 A JP 11008482A JP S6253011 B2 JPS6253011 B2 JP S6253011B2
Authority
JP
Japan
Prior art keywords
film
heat
stretching
foamed
ionomer 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
Application number
JP57110084A
Other languages
Japanese (ja)
Other versions
JPS591540A (en
Inventor
Akira Mita
Nobutaka Kishikawa
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.)
Gunze Ltd
Original Assignee
Gunze 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 Gunze Ltd filed Critical Gunze Ltd
Priority to JP11008482A priority Critical patent/JPS591540A/en
Publication of JPS591540A publication Critical patent/JPS591540A/en
Publication of JPS6253011B2 publication Critical patent/JPS6253011B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D23/00Details of bottles or jars not otherwise provided for
    • B65D23/08Coverings or external coatings
    • B65D23/0842Sheets or tubes applied around the bottle with or without subsequent folding operations
    • B65D23/0878Shrunk on the bottle

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Details Of Rigid Or Semi-Rigid Containers (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Description

【発明の詳細な説明】 本発明は緩衝効果の優れた熱収縮性を有する発
泡フイルムに関する。 従来、発泡フイルムとしてはポリスチレンから
なるものが既知であり、更に熱収縮性を併せ有す
るポリスチレンからなる発泡フイルムも既知であ
る。後者のフイルムは一般にびん等の容器類の外
装に用いられ、破びん防止や緩衝部材として役立
つていることは周知である。ところが前記のポリ
スチレンからなる熱収縮性発泡フイルムは、その
原料の特性から衝撃に弱く、いわゆる脆いという
性質があり、従つてびん等に外装しても、その輸
送中や取扱い時にフイルム端縁から砕けたりする
ことがあり、緩衝部材としての機能を充分に備え
ているとはいえず、従つて破びん効果をも低下さ
せる原因となつていた。また前記フイルムは熱収
縮させるに比較的高温が必要で、しかも熱収縮可
能な温度範囲が狭いため、熱収縮ミスを起し易く
これを防ぐために収縮工程での温度管理にも細心
の注意が必要でこのことも問題点となつていた。
更に発泡ポリスチレンは延伸の際、その脆さに起
因してか、テンター等による緯延伸がしがたく、
縦延伸ものが主流であるため、こうして製造され
たフイルムを例えばびん等の外装として使用する
際、自動包装機への適応が制限されて、従来から
使用されている緯延伸フイルム用自動包装機に適
応することが出来ず、このような使用面でも問題
点があつた。 本発明は上記のような各問題点を改善すべくな
されたものであり、熱収縮性発泡フイルムとして
第1の発明はナトリウムイオンを含むアイオノマ
ー樹脂と発泡剤とからなる組成物を成膜延伸して
なる点を特徴とするものであり、第2の発明はナ
トリウムイオンを含むアイオノマー樹脂と発泡剤
とからなる組成物を成膜延伸してなるフイルムの
少なくとも片側に熱可塑性フイルムからなるラミ
ネート層を設けた点を特徴とするものである。 以下本発明について詳述する。 本発明におけるアイオノマー樹脂としてαオレ
フインとαβ―エチレン性不飽和カルボン酸とか
ら得られるベース共重合体と水に溶解し得るイオ
ン性金属化合物とを反応させることにより得られ
る金属イオンとカルボン酸基とが結合したイオン
性共重合体を例示できる。この際前記ベース共重
合体としては、エチレン―アクリル酸共重合体、
エチレン―メタクリル酸共重合体、エチレン―マ
レイン酸共重合体、エチレン・アクリル酸―メタ
アクリル酸メチル共重合体等を例示でき、特に制
限はない。 本発明では特に前記アイオノマー樹脂にナトリ
ウムイオンを含むことが必須であり、ナトリウム
イオン以外の、例えば元素周期律表,,,
―A及び族の原子価1〜3価の金属イオン
(…Mg++,Zn++,Al+++等)を用いた場合、延伸
性が欠如し良好な発泡フイルムが得られない。 次に本発明で使用する発泡剤は、有機系のもの
としてアゾジカルボンアミド、無機系のものとし
て重炭酸ナトリウム等の炭酸塩とクエン酸等の有
機酸からなるもの等を例示でき、この他にも公知
のものを使用でき特に制限はない。そしてこの発
泡剤の使用量はアイオノマー樹脂100重量部に対
し0.2〜5重量部、好ましくは0.5〜3重量部であ
り、その用法としてこれを原料樹脂に直接ブレン
ドしたり、濃度の高い発泡剤を含むマスターペレ
ツトを加えたり、予じめ原料樹脂中に発泡剤を適
当量練り込んで用いたりすれば良い。 なお、本発明に係る組成物以外に滑剤、帯電防
止剤、その他適宜の添加剤を加えることがある。 上記のようにして作成された組成物の製膜につ
いては例えば押出成膜を行なうことができ、該組
成物を例えばダイス内で発泡しない程度に条件設
定し、ダイスから吐出すると同時に発泡するよう
にすればよく、この他公知の方法を採用すること
ができる。こうして成膜されたものを延伸するの
であるが、その温度は樹脂の軟化点以上〜融点以
下でよいが、80〜90℃の範囲が好ましい。一方倍
率は縦1軸及び緯1軸とも1.5〜5倍、好ましく
は2〜4倍で行なう。また2軸延伸する際は、縦
及び緯を上記の範囲で行えばよい。この際延伸は
従前の自動包装機、自動シール機等の適応性から
緯1軸で行なうことがより好ましく、本発明では
例えばテンターで緯延伸を行なう際も特別な配慮
を必要とせず円滑に実施できる。なおフイルムは
フラツト状として作成するとより好ましいが、他
の公知の形状で作成してもよい。 本発明は、上記のように作成したフイルムを補
強し、かつ印刷性等を向上させるため、更に適宜
の熱可塑性フイルムを、フイルムの少なくとも片
面に接着層を介し、もしくは介さずしてラミネー
ト層を設けることも可能であり、この際ラミネー
ト層としては特に原発泡フイルムと同種のナトリ
ウムイオンを含むアイオノマー樹脂からなるフイ
ルムであり、かつできるだけその厚さは薄手のも
のを用いると好適である。このラミネート方法は
共押出法、溶融押出ラミネート法その他公知の手
段を適宜採用すればよいが、原発泡フイルムと同
種の予じめ成膜されたフイルムを用いる場合、原
発泡フイルムの押出発泡直後にニツプロールによ
りラミネートすると、原発泡フイルムの押出の際
の熱により、特に加熱を要せずしてラミネートが
可能で便利である。 以上の本発明に係る熱収縮性発泡フイルムは、
その厚さが発泡後ではかなり厚くなりフイルムと
呼ぶにふさわしくないかも知れないが、本発明で
はあくまで成膜工程を経るものである関係上、厚
さに関係なく一様にフイルムという表現で統一し
た。 本発明は以上の通りであるが、このフイルムを
例えばびん等の外装用として用いると特に破びん
防止効果や緩衝効果に優れる等格別の効果を奏す
るものである。更に強度等の諸物性にも優れ、従
前のものの如く脆いという欠点もなく強靭でかつ
低温熱収縮も可能であり、かつ熱収縮の可能な温
度範囲も広いので温度管理が比較的容易で、その
収縮工程において収縮ミスが発生することもなく
極めて取扱いが容易であるという効果を有するの
である。しかも緯1軸延伸がテンターにより極め
て容易に行なえるので、実施例中緯1軸延伸によ
り作成されたフイルムは従来から使用されている
各種自動機へも適応性がよくその効果ははかり知
れぬものがある。なお用途としてはびん等の外装
用ラベルとして最も多用されるが、その他一般容
器、各種物品の包装用熱収縮部材として用いられ
特に制限はない。 次に本発明の実施例と比較例を挙げる。 〈実施例 (1)〉 Na+を含むアイオノマー樹脂100重量部に対
し、濃度の高い発泡剤の入つたマスターペレツト
のダイブローPEM20NK(大日精化(株)製;商品
名)を5重量部加え、Tダイスにより押出成膜し
て厚さ600μの発泡原反を得た。この原反を85℃
の温度でテンター内を通過させて緯方向3倍の延
伸を行い、厚さ200μの熱収縮性発泡フイルムを
得た。 〈実施例 (2)〉 実施例(1)により押出成膜された発泡原反の押出
発泡直後に、別に作成したNa+を含むアイオノマ
ー樹脂を原料とした厚さ90μのフイルムを直接ニ
ツプロールを通してラミネートしたところ、接着
強度の優れた発泡積層原反を得た。この原反を実
施例(1)と同様にテンター内を通過させて緯方向3
倍の延伸を行いラミネート層の施された熱収縮性
発泡フイルムを得た。 〈比較例 (1)〉 ポリスチレンに実施例(1)と同様の発泡剤を同量
加えてTダイスにより押出成膜し、110℃の温度
で3倍にロール延伸を行い、縦方向に熱収縮する
厚さ200μの熱収縮性発泡フイルムを得た。念の
ため、別にテンターにて緯方向に延伸しようとし
たが、き裂が入り延伸できなかつた。 以上の実施例及び比較例で得られた発泡フイル
ムの諸物性を第1表に記す。この表からも明らか
な通り、本発明のものは低温収縮性に優れかつ収
縮可能な温度範囲も広く、強靭な熱収縮性発泡フ
イルムであることが理解できる。これに対し比較
例のものは本発明のフイルムより劣ることが明白
である。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a foamed film having heat shrinkability with excellent cushioning effect. Conventionally, foamed films made of polystyrene are known, and foamed films made of polystyrene that also have heat shrinkability are also known. It is well known that the latter film is generally used for the exterior of containers such as bottles, and is useful for preventing bottle breakage and as a buffer member. However, the aforementioned heat-shrinkable foamed film made of polystyrene is susceptible to impact and is so-called brittle due to the characteristics of its raw material.Therefore, even if it is packaged in a bottle, etc., it may break from the edge of the film during transportation or handling. Therefore, it cannot be said that the buffer member has a sufficient function as a buffer member, and this also causes a decrease in the bottle-breaking effect. In addition, the film requires a relatively high temperature to be heat-shrinked, and the temperature range in which it can be shrunk is narrow, so it is easy to make mistakes in heat-shrinking, so careful attention must be paid to temperature control during the shrinking process to prevent this. This also became a problem.
Furthermore, when polystyrene foam is stretched, it is difficult to weft-stretch it using a tenter, etc., perhaps due to its brittleness.
Because longitudinally stretched films are the mainstream, when using films produced in this way as exterior packaging for bottles, for example, their application to automatic packaging machines is limited, and the conventional automatic packaging machines for weft-stretched films cannot be used. It was not possible to adapt the method, and there were problems in this kind of usage. The present invention has been made in order to improve each of the above-mentioned problems, and the first invention as a heat-shrinkable foamed film is made by forming and stretching a composition consisting of an ionomer resin containing sodium ions and a foaming agent. The second invention is characterized in that a laminate layer made of a thermoplastic film is provided on at least one side of a film formed by forming and stretching a composition made of an ionomer resin containing sodium ions and a foaming agent. It is characterized by the following points. The present invention will be explained in detail below. The ionomer resin used in the present invention includes metal ions and carboxylic acid groups obtained by reacting a base copolymer obtained from α-olefin and αβ-ethylenically unsaturated carboxylic acid with an ionic metal compound that can be dissolved in water. An example is an ionic copolymer in which At this time, as the base copolymer, ethylene-acrylic acid copolymer,
Examples include ethylene-methacrylic acid copolymer, ethylene-maleic acid copolymer, ethylene-acrylic acid-methyl methacrylate copolymer, and there are no particular limitations. In the present invention, it is particularly essential that the ionomer resin contains sodium ions, and other elements other than sodium ions, such as those of the periodic table of elements,...
-A and group monovalent to trivalent metal ions (...Mg ++ , Zn ++ , Al +++, etc.) lack stretchability and a good foamed film cannot be obtained. Next, the blowing agent used in the present invention can be exemplified by azodicarbonamide as an organic type, and one consisting of a carbonate such as sodium bicarbonate and an organic acid such as citric acid as an inorganic type. Also, any known material can be used and there are no particular limitations. The amount of this blowing agent used is 0.2 to 5 parts by weight, preferably 0.5 to 3 parts by weight, per 100 parts by weight of the ionomer resin. The foaming agent may be used by adding master pellets containing the foam or by kneading an appropriate amount of a blowing agent into the raw resin in advance. In addition to the composition according to the present invention, a lubricant, an antistatic agent, and other appropriate additives may be added. For film formation of the composition created as described above, for example, extrusion film formation can be performed, and conditions are set so that the composition does not foam in a die, so that the composition foams at the same time as it is discharged from the die. Any other known method may be used. The film formed in this way is stretched at a temperature ranging from the softening point to the melting point of the resin, preferably from 80 to 90°C. On the other hand, the magnification is 1.5 to 5 times, preferably 2 to 4 times in both the vertical axis and the latitude axis. Further, when biaxially stretching, the longitudinal and latitudinal stretching may be carried out within the above ranges. At this time, it is more preferable to carry out the stretching in one weft axis from the viewpoint of adaptability to conventional automatic packaging machines, automatic sealing machines, etc. In the present invention, for example, when carrying out weft stretching with a tenter, it can be carried out smoothly without requiring special consideration. can. Although it is more preferable that the film be made in a flat shape, it may be made in other known shapes. In the present invention, in order to reinforce the film produced as described above and improve printability, etc., a suitable thermoplastic film is further coated with a laminate layer on at least one side of the film with or without an adhesive layer. In this case, it is preferable to use a film made of an ionomer resin containing the same kind of sodium ions as the original foamed film and as thin as possible as the laminate layer. For this lamination method, coextrusion, melt extrusion lamination, or other known methods may be adopted as appropriate. However, when using a pre-formed film of the same type as the original foamed film, immediately after the extrusion foaming of the original foamed film, When laminated with Nipprol, the heat generated during extrusion of the original foamed film allows lamination to be carried out without the need for particular heating, which is convenient. The above heat-shrinkable foam film according to the present invention is
The thickness becomes quite thick after foaming, and it may not be appropriate to call it a film, but since the present invention involves a film formation process, the term "film" is used uniformly regardless of the thickness. . The present invention has been described above, and when this film is used for the exterior of bottles, for example, it exhibits exceptional effects such as excellent bottle breakage prevention effects and cushioning effects. Furthermore, it has excellent physical properties such as strength, is strong without the drawback of brittleness like previous products, and can be heat-shrinked at low temperatures.The temperature range in which heat-shrinkage is possible is also wide, so temperature control is relatively easy. This has the advantage of being extremely easy to handle without causing shrinkage errors during the shrinkage process. Moreover, since the weft uniaxial stretching can be carried out extremely easily using a tenter, the film produced by the mid-latitude uniaxial stretching in the example is highly adaptable to various automatic machines that have been used in the past, and its effects are immeasurable. There is. Although it is most frequently used as an exterior label for bottles and the like, it can also be used as a heat-shrinkable member for packaging general containers and various articles, and is not particularly limited. Next, examples of the present invention and comparative examples will be given. <Example (1)> To 100 parts by weight of ionomer resin containing Na + , 5 parts by weight of master pellet Dive-Blow PEM20NK (manufactured by Dainichiseika Kaisha, Ltd.; trade name) containing a highly concentrated blowing agent was added. A foamed original fabric having a thickness of 600 μm was obtained by extrusion using a T die. 85℃
A heat-shrinkable foamed film with a thickness of 200 μm was obtained by passing it through a tenter at a temperature of 3 times the width in the weft direction. <Example (2)> Immediately after extrusion foaming of the foamed fabric formed by extrusion in Example (1), a separately prepared 90μ thick film made from an ionomer resin containing Na + was laminated through a Nitpro roll directly. As a result, a foamed laminated original fabric with excellent adhesive strength was obtained. This original fabric was passed through the tenter in the same manner as in Example (1), and
A heat-shrinkable foamed film with a laminate layer was obtained by stretching the film twice as much. <Comparative example (1)> Add the same amount of the same blowing agent as in Example (1) to polystyrene, extrude it into a film using a T-die, roll stretch it three times at a temperature of 110°C, and heat shrink it in the longitudinal direction. A heat-shrinkable foamed film with a thickness of 200μ was obtained. Just to be sure, I tried to stretch it in the weft direction using a tenter, but cracks appeared and I couldn't stretch it. Table 1 shows the physical properties of the foamed films obtained in the above Examples and Comparative Examples. As is clear from this table, it can be seen that the film of the present invention has excellent low-temperature shrinkability, has a wide range of shrinkable temperatures, and is a strong heat-shrinkable foamed film. On the other hand, it is clear that the films of the comparative examples are inferior to the films of the present invention. 【table】

Claims (1)

【特許請求の範囲】 1 ナトリウムイオンを含むアイオノマー樹脂と
発泡剤とからなる組成物を成膜延伸してなること
を特徴とする熱収縮性発泡フイルム。 2 延伸が緯方向に1軸である特許請求の範囲第
1項記載の熱収縮性発泡フイルム。 3 ナトリウムイオンを含むアイオノマー樹脂と
発泡剤とからなる組成物を成膜延伸してなるフイ
ルムの少なくとも片側に熱可塑性フイルムからな
るラミネート層を設けたことを特徴とする熱収縮
性発泡フイルム。 4 延伸が緯方向に1軸である特許請求の範囲第
3項記載の熱収縮性発泡フイルム。 5 熱可塑性フイルムがナトリウムイオンを含む
アイオノマー樹脂を主成分とする特許請求の範囲
第3項記載の熱収縮性発泡フイルム。
[Scope of Claims] 1. A heat-shrinkable foamed film produced by forming and stretching a composition comprising an ionomer resin containing sodium ions and a foaming agent. 2. The heat-shrinkable foamed film according to claim 1, wherein the stretching is uniaxial in the weft direction. 3. A heat-shrinkable foamed film, characterized in that a laminate layer made of a thermoplastic film is provided on at least one side of a film formed by forming and stretching a composition made of an ionomer resin containing sodium ions and a foaming agent. 4. The heat-shrinkable foamed film according to claim 3, wherein the stretching is uniaxial in the weft direction. 5. The heat-shrinkable foamed film according to claim 3, wherein the thermoplastic film is mainly composed of an ionomer resin containing sodium ions.
JP11008482A 1982-06-25 1982-06-25 Heat-shrinkable expanded film Granted JPS591540A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11008482A JPS591540A (en) 1982-06-25 1982-06-25 Heat-shrinkable expanded film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11008482A JPS591540A (en) 1982-06-25 1982-06-25 Heat-shrinkable expanded film

Publications (2)

Publication Number Publication Date
JPS591540A JPS591540A (en) 1984-01-06
JPS6253011B2 true JPS6253011B2 (en) 1987-11-09

Family

ID=14526619

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11008482A Granted JPS591540A (en) 1982-06-25 1982-06-25 Heat-shrinkable expanded film

Country Status (1)

Country Link
JP (1) JPS591540A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH074190Y2 (en) * 1988-04-06 1995-02-01 東洋製罐株式会社 Hollow container with label

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5336573A (en) * 1970-11-24 1978-04-04 Owens Illinois Inc Sheet of extruded thermal plastic* shrinkable material
JPS5667249A (en) * 1979-11-08 1981-06-06 Sumitomo Bakelite Co Plastic film for packing and its manufacture
JPS57135121A (en) * 1981-02-16 1982-08-20 Sumitomo Bakelite Co Ltd Manufacture of oriented plastic film

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5336573A (en) * 1970-11-24 1978-04-04 Owens Illinois Inc Sheet of extruded thermal plastic* shrinkable material
JPS5667249A (en) * 1979-11-08 1981-06-06 Sumitomo Bakelite Co Plastic film for packing and its manufacture
JPS57135121A (en) * 1981-02-16 1982-08-20 Sumitomo Bakelite Co Ltd Manufacture of oriented plastic film

Also Published As

Publication number Publication date
JPS591540A (en) 1984-01-06

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