JPS60118729A - Stretch film - Google Patents

Stretch film

Info

Publication number
JPS60118729A
JPS60118729A JP22558983A JP22558983A JPS60118729A JP S60118729 A JPS60118729 A JP S60118729A JP 22558983 A JP22558983 A JP 22558983A JP 22558983 A JP22558983 A JP 22558983A JP S60118729 A JPS60118729 A JP S60118729A
Authority
JP
Japan
Prior art keywords
film
chloride resin
stretch film
tensile load
weight
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
Application number
JP22558983A
Other languages
Japanese (ja)
Inventor
Shinzo Otsu
晋三 大津
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.)
Mitsubishi Plastics Inc
Original Assignee
Mitsubishi Plastics Inc
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 Mitsubishi Plastics Inc filed Critical Mitsubishi Plastics Inc
Priority to JP22558983A priority Critical patent/JPS60118729A/en
Publication of JPS60118729A publication Critical patent/JPS60118729A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a stretch film of vinyl chloride resin having improved printability on the surface of the film, obtained by blending polyvinyl chloride resin with specific amounts of specified stabilizer and anti-fogging agent, providing the blend with specific elongation characteristics. CONSTITUTION:(A) 100pts.wt. polyvinyl chloride resin is blended with (B) 15- 60pts.wt. plasticizer (e.g., adipic acid ester of higher alcohol, etc.) to give a stretch film, which is blended with (C) Ca-Zn liquid stabilizer and (D) 2-3pts.wt. total amounts of D1 and D2 of anti-fogging agent consisting of D1: polyoxyethylene alkyl ether having 4-20mol of ethylene oxide addition and 12-20C alkyl group and D2: sorbitan fatty acid ester comprising a fatty acid containing 9- 17C alkyl group in a ratio of D1:D2 of (1:1)-(1:1.5). The composition is melted under heating, and molded to give a film having 120-300g/cm longitudinal tensile load and 30-60g/cm lateral tensile load at 25% elongation measured at 200mm./ min stress rate.

Description

【発明の詳細な説明】 本発明はストレンチフィルムに係り、特にフィルム表面
への印刷適性に優れた塩化ビニル樹脂製ストレッチフィ
ルムに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a stretch film, and particularly to a stretch film made of vinyl chloride resin that has excellent printability on the film surface.

食品等の包装手段として、フィルムを引き伸ばしつつ物
品を包み込み、該フィルムの折返し端部な指などで軽く
圧着するだけで該フィルムの端部同志を粘着(自己粘着
)させて包装する、いわゆるストレンチ包装がスーパー
マーケット等で一般的に行なわれている。
So-called stretch packaging is used as a means of packaging foods, etc., in which the product is wrapped while being stretched, and the ends of the film are made to stick (self-adhesive) together by simply pressing the folded ends of the film lightly with fingers or the like. This is commonly done in supermarkets, etc.

上記ストレンチ包装には、ポリ塩化ビニル樹脂に可塑剤
を添加した塩化ビニル樹脂製ストレンチフィルムが、透
明性及び自己粘着性等に優れており、最も多用されてい
る。
For the above-mentioned trench packaging, a vinyl chloride resin trench film, which is made by adding a plasticizer to polyvinyl chloride resin, is most commonly used because it has excellent transparency and self-adhesiveness.

一方、包装料においては、包装内容物の表示等を表面に
印刷することが、その品質表示、宣伝機能として要望さ
れる。しかしながら、上記の塩化ビニル樹脂製ストレン
チフィルムに印刷を施す場合、フィルム自体の特性でお
るフィルムの伸ひ易さのため印刷柄ずれが起とりやすく
、また印刷後には、添加した可塑剤等がフィルム表面に
吹出す(ブリード)ため、印刷インキが表面から剥離し
他フィルムへ転写(裏写シ)するというトラブルが起こ
りやすい。
On the other hand, for packaging materials, it is desired to print information such as the contents of the package on the surface as a quality display and advertising function. However, when printing on the above-mentioned PVC resin stretch film, misalignment of the printed pattern is likely to occur due to the ease of stretching of the film due to the characteristics of the film itself, and after printing, the added plasticizer etc. Since the printing ink is blown out onto the film surface (bleed), troubles such as the printing ink peeling off from the surface and being transferred to other films (bleeding) are likely to occur.

本発明は上記問題点を解消するため特定の組成物を使用
し、特定の引張り伸び特性を有するストレッチフィルム
を見出したものであって、その要旨とするところは、 ポリ塩化ビニル系樹脂100重量部に対し可塑剤を73
−〜乙0重量部混合してなるストレンチフィルムにおい
て、安定剤としてC!a−Zn 系液状安定剤、並びに
防曇剤として (A) ポリオキシエチレンアルキルエーテル、及び (B) ソルビタン脂肪酸エステル を添加してなり、上記(Nと(Blの重量比が/:/〜
/ : /、3の範囲内で、かつ(AlとCB+との合
計量が2.0〜3.0重量部の範囲内にあり、該フィル
ムの引張速度、xoown1分で測定した2t%伸長時
の引張荷重が縦方向/20〜J 00117cm、横方
向30〜60?/cmであること−を特徴とするストレ
ッチフィルムにある。
In order to solve the above-mentioned problems, the present invention uses a specific composition and has discovered a stretch film having specific tensile elongation characteristics. 73% plasticizer
-~ In the trench film formed by mixing 0 parts by weight of C, as a stabilizer! It is made by adding (A) polyoxyethylene alkyl ether and (B) sorbitan fatty acid ester as an a-Zn-based liquid stabilizer and an antifogging agent, and the weight ratio of the above (N and (Bl) is /:/ ~
/: /, within the range of 3, and (the total amount of Al and CB+ is within the range of 2.0 to 3.0 parts by weight, and the tensile speed of the film is 2t% elongation measured at xoown 1 minute) The stretch film is characterized by having a tensile load of 20 to 60 cm in the longitudinal direction and 30 to 60 cm in the transverse direction.

本発明フィルムの主成分であるポリ塩化ビニル系樹脂(
以下rPVOJという。)及び可塑剤は、通常用いられ
ているものでよく、pvcとしては単独重合体または少
量の他成分を含む共重合体が使用される。また、可塑剤
としては、高級アルコールのアジピン酸エステノペエボ
キシ化植物油等が挙げられ、その量はPVO100重量
部に対し75〜60重量部の範囲とする。
Polyvinyl chloride resin (
Hereinafter referred to as rPVOJ. ) and plasticizers may be those commonly used, and the PVC used may be a homopolymer or a copolymer containing small amounts of other components. Further, examples of the plasticizer include adipic acid ester epoxylated vegetable oil, which is a higher alcohol, and the amount thereof is in the range of 75 to 60 parts by weight per 100 parts by weight of PVO.

本発明フィルムの安定剤は、CaZn系液状安定剤を使
用する。該安定剤は常温で液状であることが必要であっ
て、ステアリン酸Oa等の粉末状金属石鹸類の使用は、
添加剤のフィルム表面への吹出しを促進するため不都合
である。
As the stabilizer for the film of the present invention, a CaZn-based liquid stabilizer is used. The stabilizer must be liquid at room temperature, and the use of powdered metal soaps such as stearic acid Oa
This is disadvantageous because it promotes blowing of the additive onto the film surface.

本発明フィルムに防曇性及び適度の滑り性を付与するた
めの防曇剤としては、前記(A)ポリオキシエチレンア
ルキルエーテルと(B)ソルビタン脂肪酸エステルの組
合せのものを使用する必要がある。(AJのポリオキシ
エチレンアルキルエ−テル 75=<z〜.?0で、炭素数/2〜.20のアルキル
基からなるもので、具体的には、ポリオキンエチレンラ
ウリルエーテルやポリオキシエチレンステアリルエーテ
ル等が挙げられる。(Blのソルビタン脂肪酸エステル
としては、炭素数7〜/7のアルキル基を有する脂肪酸
からなるものであり、具体的にはソルビタンラウリン酸
エステルやソルビタンミリスチン酸エステル等が挙げら
れる。
As the antifogging agent for imparting antifogging properties and appropriate slipperiness to the film of the present invention, it is necessary to use a combination of the above-mentioned (A) polyoxyethylene alkyl ether and (B) sorbitan fatty acid ester. (AJ polyoxyethylene alkyl ether 75=<z~.?0 and consists of an alkyl group with carbon number/2~.20, specifically, polyoxyethylene lauryl ether and polyoxyethylene stearyl (The sorbitan fatty acid ester of Bl is composed of a fatty acid having an alkyl group having 7 to 7 carbon atoms, and specific examples thereof include sorbitan laurate and sorbitan myristate. .

添加比率については、(A)と(131の重量比が/:
/〜/ : /.!;で、かつ(A)と(B)との合側
量を2.0〜3.0重沿部の範囲とする。上記比率で(
Blが7未満のものは防曇性に劣り、/.jを越えるも
のについては、フィルム表面に吹出しが多くなシ印刷イ
ンキの転写が起こシやすい。
Regarding the addition ratio, the weight ratio of (A) and (131 is /:
/〜/:/. ! ; and the amount of joining of (A) and (B) is in the range of 2.0 to 3.0 folds. At the above ratio (
Those with Bl less than 7 have poor antifogging properties, and /. If the value exceeds j, transfer of printing ink is likely to occur with many blowouts on the film surface.

なお、上述した添加剤の他に必要に応じて、キレ−クー
や着色剤等を添加してもよい。
In addition to the above-mentioned additives, a coloring agent or the like may be added as necessary.

つき゛に、上記内容からなる組成物を加熱溶融後、押出
機から押出して製膜する。
First, a film is formed by heating and melting the composition having the above contents and then extruding it from an extruder.

製膜後のフィルムは、特定の引張伸び特性を有すること
が必要であシ、引張速度20θ咽/分で測定した、2t
%伸長時の引張荷重を縦方向7、20〜3oof/er
r.、横方向30〜乙O f/cmの範囲とする。
The film after film formation must have a specific tensile elongation property, which is 2t measured at a tensile rate of 20θ/min.
% elongation tensile load in longitudinal direction 7, 20 to 3 oof/er
r. , in the range of 30 to 30 f/cm in the lateral direction.

この特性を付与する理由は、フィルム表面にグラビア印
刷等の方法により印刷を施す場合、フィルム縦方向に印
刷機のロール間の張力が加わりフィルムが伸びて、柄ず
れが発生するため、フィルム縦方向の伸びは出来るだけ
小さい方が良く、上記引張荷重で/2θ!/lyn以上
が必要である。しかし、3009/lynを越えるもの
では、印刷工程で不均一なしわ入りが発生し易く、不都
合である。また最終的にストレソナ包装を行なう場合、
通常フィルム横方向に引き伸ばして包装するため、フィ
ルム横方向へは適度の伸びやすさを有するものが包装時
の作業性がよく、上記引張荷重で6097cm以下とす
る必要がある。
The reason for giving this property is that when printing on the film surface using a method such as gravure printing, tension between the rolls of the printing machine is applied in the longitudinal direction of the film, stretching the film and causing pattern misalignment. It is better to have the elongation as small as possible, and at the above tensile load /2θ! /lyn or higher is required. However, if it exceeds 3009/lyn, uneven wrinkles are likely to occur during the printing process, which is disadvantageous. In addition, when final packaging is performed,
Since the film is usually stretched in the transverse direction for packaging, a film that has moderate stretchability in the transverse direction has good workability during packaging, and the above tensile load must be 6097 cm or less.

しかし、3t)97cm未満では縦方向のフィルレム伸
びへ影響し、縦伸びが大きくなるため不都合である。
However, if it is less than 3t)97cm, it will affect the fillem elongation in the longitudinal direction and increase the longitudinal elongation, which is disadvantageous.

上記の引張伸び特性を付与するためのフィルム製造条件
は、使用する成形機によって異なるが、Tダイ法による
場合、押出機口金直後の冷却ロール速度と最終の巻取ロ
ール速度との比をへ/S〜/、j程度とすることにより
得ることができる。
The film manufacturing conditions for imparting the above tensile elongation properties vary depending on the molding machine used, but when using the T-die method, the ratio of the cooling roll speed immediately after the extruder mouth to the final take-up roll speed is set to / It can be obtained by setting it to about S~/,j.

つぎに、本発明を実施例にょシ詳細に説明する。Next, the present invention will be explained in detail using examples.

実施例/ PVO/θθ重量部に、可塑剤4I−5重量部(ジイソ
ノニルアジペート30重量部、エポキシ化大豆油/ J
’ fi 置部) C!a−Zn系液状安定剤7重量部
、及び防曇剤として表−/記載の内容物からなる組成物
を加熱混合して、押出様から溶融押出して、厚さ/gμ
のストレンチフィルムを得た。なお、比較品−について
は、上記0a−Zn系液状安定剤の代わりに粉末のステ
アリン酸Oa及びステアリン酸Znを各々0.7重量部
添加したものである。得られた各フィルムの防曇性、イ
ンキ印刷性及びインキ転写性の評価結果を表−/に示し
た。
Example / PVO/θθ weight parts, plasticizer 4I-5 weight parts (diisononyl adipate 30 weight parts, epoxidized soybean oil/J
'fi Okabe) C! A composition consisting of 7 parts by weight of a-Zn liquid stabilizer and the contents listed in Table 1 as an antifogging agent was heated and mixed, and the mixture was melt-extruded in an extrusion mode to obtain a thickness/gμ.
A trench film was obtained. As for the comparative product, 0.7 parts by weight of each of powdered stearic acid Oa and stearic acid Zn were added instead of the Oa-Zn liquid stabilizer. The evaluation results of the antifogging properties, ink printability, and ink transferability of each film obtained are shown in Table 1.

各性能の評価方法は次の通シである。The evaluation method for each performance is as follows.

/)防曇性 7に一20℃のたて切シきゆうシをトレーに入れ、各フ
ィルムで開口部を覆って約S℃冷蔵ケースに入れた。1
0分後にとシ出してフィルムの曇り度合をみて全く曇り
のないもの(◎)、フィルム内面に大きな水滴が付着し
ているが、中味はきれいに見えるもの(○)、中味がよ
く見えないもの(×)とした。
/) Anti-fogging property 7: Place the freshly cut pieces at -20°C into a tray, cover the openings with each film, and place in a refrigerated case at about S°C. 1
After 0 minutes, remove the film and check the degree of cloudiness. There is no clouding at all (◎), there are large water droplets on the inside of the film but the contents are clearly visible (○), and the contents are not clearly visible (○). x).

りインキ印刷性 東洋インキ製造■製インキ、xgo、:zvcを使用し
グラビア印刷を施した各フィルムの印刷面に市販のセロ
ファンテープを貼着し、このテープを剥した時のインキ
の剥れ具合をみた。全くインキの剥れかないもの(◎)
、わずかに剥れがみられるもの(○)、テープを剥した
印刷面の約半分のインキが剥れたもの(×)とした。
Ink printing properties Commercially available cellophane tape was attached to the printed surface of each film that was gravure printed using Toyo Ink Manufacturing ■ ink, XGO, :ZVC, and the degree of ink peeling when the tape was peeled off. I saw it. Ink that does not peel off at all (◎)
, those with slight peeling (○), and those with about half of the ink peeled off from the printed surface from which the tape was removed (x).

3〕 インキ転写性 東洋インキ製造■製インキ、xro、zvaを使用しグ
ラビア印刷したフィルムを巻物として、jj℃の雰囲気
中に!日間放置した後インキの転写の有無をみた。印刷
面に接触したフィルムにインキの転写が全くないもの(
◎)、わずかにインキの転写がみもれるが、実用上問題
がないもの(○)、印刷面のほぼ半分くらいが転写した
もの(△)とした。
3] Ink transferability A roll of gravure-printed film using Toyo Ink Manufacture's ink, XRO, and ZVA is placed in an atmosphere at JJ℃! After leaving it for a day, the presence or absence of ink transfer was checked. There is no transfer of ink to the film that comes into contact with the printing surface (
◎), a slight ink transfer was observed but there was no practical problem (○), and approximately half of the printed surface was transferred (△).

表−/ POELE ; ポリオギンエチレンラウリルエーテル
SML ; ソルビタンモノラウレートPGMO; ポ
リグリセリンモノオレー1・GMO; グリセリンモノ
オレー1・ 表−/から明らかなように、本発明の実施品/、スは、
3つの性能ともに優れていることが判る。
Table - / POELE; Polyogine ethylene lauryl ether SML; Sorbitan monolaurate PGMO; Polyglycerin monoole 1 GMO; Glycerin monoole 1 As is clear from Table - /, the products of the present invention are:
It can be seen that all three performances are excellent.

これに対し、本発明の防曇剤を使用しているが、添加部
数の少ない比較品/及び粉末状安定剤を使用している比
較品ノについて&′:1、防曇性に劣り、本発明と防赫
剤が異なる比較品3〜3についても3つの性能のいずれ
かが劣っていることが判る。
On the other hand, the comparative products using the antifogging agent of the present invention but with a small number of additives/and the comparative products using powdered stabilizers were inferior in antifogging properties; It can be seen that Comparative Products 3 to 3, which have different anti-fouling agents from those of the invention, are also inferior in one of the three performances.

実施例! 配合内容を実施例/の実施品/と同一とし、高速ミキサ
ーで加熱混合後、Tダイ法にて押出温度200℃で押出
ノ成形した。
Example! The composition was the same as that of the product in Example/, and after heating and mixing with a high speed mixer, extrusion molding was performed using a T-die method at an extrusion temperature of 200°C.

この場合、Tダイ口金直後の冷却ロール速度と最終の巻
取ロール速度との比を表−!に示した比とし、口金ギヤ
ツブや温度条件等を適宜変えて、各々/gμの厚みを有
するフィルムを得た。各フィルムについて、引張速度、
200 ran/分で引張試験を行ない、2j%伸長時
の引張荷重をフィルムの縦方向と横方向で測定した。ま
た各フィルムにつき、東洋インキ製造■製、Xg02V
C3色を使用しグラビア多色印刷機により印刷を施し、
印刷の柄ずれを測定した。
In this case, the ratio between the cooling roll speed immediately after the T-die die and the final take-up roll speed is shown in the table below. By using the ratios shown in , and changing the mouth gear, temperature conditions, etc. as appropriate, films having a thickness of /gμ were obtained. For each film, the tensile speed,
A tensile test was conducted at 200 ran/min, and the tensile load at 2j% elongation was measured in the longitudinal and transverse directions of the film. In addition, for each film, manufactured by Toyo Ink Manufacturing ■, Xg02V
Printed using a gravure multicolor printing machine using C3 colors,
The pattern misalignment in printing was measured.

測定結果を表−一に示した。柄ずれが0.7m以下の優
れたものは(◎〕、09.!〜0.11 amで良好な
もの(○)、O,S〜0.ly m++1で見苦しいも
の(△)、θ、6閾を越すもので非常に見苦しいもの(
×)としだ。
The measurement results are shown in Table 1. Excellent ones with pattern deviation of 0.7 m or less (◎), good ones with 09.!~0.11 am (○), unsightly ones with O,S~0.ly m++1 (△), θ, 6 Something that crosses the threshold and is extremely unsightly (
×) Toshida.

表−2 表−ノから、本発明の範囲である試料阻3〜jについて
は柄ずれが少なく良好であることが判る。縦方向の引張
荷重が小さい試料醜/、λ及び横方向の引張仇重が小さ
すき゛る試料N116については柄ずれが大きいことが
判る。1だ縦方向の引張荷重が太きすぎる試料M7につ
いては、印刷時フィルムに不均一なしわ入りが発生し、
良好な印刷が出来なかった。
Table 2 From Table 2, it can be seen that samples 3 to j, which are within the scope of the present invention, are good with little pattern deviation. It can be seen that the handle misalignment is large for the sample N116, which has a small tensile load in the longitudinal direction, and the sample N116, which has a small tensile load in the horizontal direction. For sample M7, in which the tensile load in the longitudinal direction was too thick, uneven wrinkles occurred in the film during printing.
Good printing was not possible.

Claims (1)

【特許請求の範囲】 ポリ塩化ビニル系樹脂700重量部に対し可塑剤を7j
〜60重量部混合してなるストレッチフィルムにおいて
、安定剤としてCa −Zn系液状安定剤、並びに防曇
剤として、 +Al ポリオキンエチレンアルキルエーテル、及び (BJ ンルビタン脂肪酸エステル を添加してな9、上記(A)と(BJの重量比が/二/
〜/ : t、Sの範囲内で、かつ[A)とtB)との
合計量が2,0〜3.0重量部の範囲内にあり、該フィ
ルムの引張速度、:xovtan/分で測定したx、r
%伸長時の引張荷重が縦方向/、2θ〜300117c
m、横方向30〜乙Of7cmであることを特徴とする
ストレンチフィルム。
[Claims] 700 parts by weight of polyvinyl chloride resin and 7j of plasticizer.
In the stretch film formed by mixing ~60 parts by weight, a Ca-Zn liquid stabilizer is added as a stabilizer, and +Al polyquine ethylene alkyl ether and (BJ Nrubitan fatty acid ester) are added as an antifogging agent. The weight ratio of (A) and (BJ is /2/
~/: within the range of t, S, and the total amount of [A) and tB) is within the range of 2.0 to 3.0 parts by weight, and the tensile speed of the film is measured at xovtan/min. x, r
% tensile load at elongation in longitudinal direction /, 2θ ~ 300117c
A stretch film characterized by having a width of 30 to 7 cm in the horizontal direction.
JP22558983A 1983-11-30 1983-11-30 Stretch film Pending JPS60118729A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22558983A JPS60118729A (en) 1983-11-30 1983-11-30 Stretch film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22558983A JPS60118729A (en) 1983-11-30 1983-11-30 Stretch film

Publications (1)

Publication Number Publication Date
JPS60118729A true JPS60118729A (en) 1985-06-26

Family

ID=16831679

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22558983A Pending JPS60118729A (en) 1983-11-30 1983-11-30 Stretch film

Country Status (1)

Country Link
JP (1) JPS60118729A (en)

Similar Documents

Publication Publication Date Title
US4666778A (en) Packaging film and sheet capable of forming peelable seals with good optics
EP0970144B1 (en) Improved antifog composition for polyolefin packaging films
EP0141555A1 (en) Oriented polymeric films, packaging made from such films and methods of making the films and packaging
CN110539538B (en) Cast CPE (chlorinated polyethylene) inflatable automatic packaging composite film and preparation method thereof
JP2010502770A5 (en)
JPH0371465B2 (en)
US5043040A (en) Slitting of plastic film
EP0178061B1 (en) Packaging film or sheet
JPS5836412A (en) Manufacture of film from compound of ethylene/vinyl alcohol copolymer and nylon and film oriented
JPS5920345A (en) Plasticized ethylene/vinyl alcohol copolymer blend, use and product
EP0011930A1 (en) Blends of polyethylene and polybutene and films made from the blends
JPS60118729A (en) Stretch film
US5128205A (en) Improved slitting of plastic film
JP3606652B2 (en) Method for producing stretch film for food packaging
JPH0547384B2 (en)
JP2894120B2 (en) Stretch wrap multilayer film
JP2894121B2 (en) Stretch wrap multilayer film
JPH0673202A (en) Biaxially oriented polypropylene film
JPH05278179A (en) Multilayered stretch-wrap film
JP3124346B2 (en) Stretch wrap multilayer film
JPS6044541A (en) Vinyl chloride resin composition for stretch film
JPS6185457A (en) Propylene copolymer composition
JP2000289158A (en) Film for stretch packaging
JP2003011298A (en) Stretch-packaging film
WO2020262249A1 (en) Stretch packaging film