JPH01133737A - Polyethylene composite film - Google Patents

Polyethylene composite film

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Publication number
JPH01133737A
JPH01133737A JP62291952A JP29195287A JPH01133737A JP H01133737 A JPH01133737 A JP H01133737A JP 62291952 A JP62291952 A JP 62291952A JP 29195287 A JP29195287 A JP 29195287A JP H01133737 A JPH01133737 A JP H01133737A
Authority
JP
Japan
Prior art keywords
film
layer
crosslinked
heat
polyethylene
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
JP62291952A
Other languages
Japanese (ja)
Other versions
JPH0528989B2 (en
Inventor
Yasushi Itaba
板場 康
Hiroshi Yoshifuji
吉藤 寛
Takayoshi Kondo
隆義 近藤
Ichiro Sakamoto
阪本 一郎
Tadao Yoshino
忠雄 吉野
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.)
Tonen General Sekiyu KK
Original Assignee
Toa Nenryo Kogyyo KK
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 Toa Nenryo Kogyyo KK filed Critical Toa Nenryo Kogyyo KK
Priority to JP62291952A priority Critical patent/JPH01133737A/en
Priority to US07/268,498 priority patent/US5006378A/en
Priority to KR1019880014792A priority patent/KR910008697B1/en
Priority to EP19880310726 priority patent/EP0317237A3/en
Publication of JPH01133737A publication Critical patent/JPH01133737A/en
Publication of JPH0528989B2 publication Critical patent/JPH0528989B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To contrive improvements in moisture resistance, flexocrack resistance, cutting properties and heat-sealing properties, by a method wherein a kind of a laminating material having a specific shrinkage factor is laminated to one side of a polyethylene stretched film whose degree of crosslinking has been deteriorated inward in the direction of a thickness. CONSTITUTION:A BOPE film which becomes a base material layer is of a polyethylene biaxially stretched film whose degree of crosslinking has been deteriorated inward in the direction of a film thickness. It is preferable that the inside lowest gel content rate is 0%, gel content rate of an outside crosslinked layer falls within a range of 20-70% both sides of which are crosslinked identically, a crosslinked layer/an uncrosslinked layer/the crosslinked layer are constituted in the direction of the film thickness and a constituted ratio among layers each falls within a range of the uncrosslinked layer : both the side crosslinked layers = 1:0.1-10. Then paper or Al foil or cellophane or heat-resistant resin film whose heat shrinkage factor at 140 deg.C is less than 5% is made a laminating material. A thickness of a composite film obtained by laminating the BOPE film of the base material and at least a kind of the above-mentioned laminating material together is selected appropriately according to the purpose and use of packaging and it is normally about 20-200mum.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、防湿性に優れ耐フレキンクラック性、カット
性及びヒートシール性を合せ持った、包装用に好適なポ
リエチレン複合フィルムに関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a polyethylene composite film suitable for packaging, which has excellent moisture resistance, flexible crack resistance, cuttability, and heat sealability.

従来の技術 従来、一般包装用フイルムとしては、表基材が紙、ポリ
エチレンテレフタレートフィルム(PKTF)、二軸延
伸ポリプロピレンフィルム(OP p ) 、セロファ
ン、延伸ポリアミドフィルム(opA)等の耐熱性基材
、中間基材がエチレン−酢酸ビニル共重合体ケン化物の
フイにム(BVAケン化物)、アルミニウム(ht)箔
等のガスバリヤ−層及びシール基材の3層構成となるも
のが知られている。しかし、これらの表基材は、耐フレ
キソクラック性、防湿性、カット性等が十分でなく、中
間基材の性能を十分に補えないという問題がある。又、
上記表基材は、例えばガセット袋等表基材同士のシール
性が要求される用途においてはシール性がなく、さらに
クール基材を設けることが必要となるためコストアンプ
につながる。
Conventional technology Conventionally, general packaging films include paper, heat-resistant base materials such as polyethylene terephthalate film (PKTF), biaxially oriented polypropylene film (OPp), cellophane, oriented polyamide film (OPA), etc. A three-layer structure is known in which the intermediate base material is a film of saponified ethylene-vinyl acetate copolymer (saponified BVA), a gas barrier layer such as aluminum (HT) foil, and a seal base material. However, these front base materials have a problem in that they do not have sufficient flexo crack resistance, moisture resistance, cuttability, etc., and cannot sufficiently compensate for the performance of the intermediate base material. or,
The above-mentioned front base material does not have sealing performance in applications such as gusset bags that require sealing performance between the front base materials, and furthermore, it is necessary to provide a cool base material, which leads to cost increase.

一方、既にフィルムの厚さ方向の架橋度が特定構成をし
た防湿性及び透明性に優れる架橋ポリエチレン延伸フィ
ルムと低密ポリエチレン等のシーラント層とからなるポ
リエチレン複合フィルムが提案された(特開昭60−1
71149号公報)。しかし、このポリエチレン複合フ
ィルムも、架橋ポリエチレン延伸フィルム同士のヒート
シール性においては問題が残されている。
On the other hand, a polyethylene composite film consisting of a cross-linked polyethylene stretched film with excellent moisture resistance and transparency with a specific cross-linking degree in the film thickness direction and a sealant layer such as low-density polyethylene has already been proposed (Japanese Unexamined Patent Application Publication No. 1989-1999). -1
71149). However, this polyethylene composite film also has a problem in heat sealability between stretched crosslinked polyethylene films.

本発明は、上記従来の問題点を解消すべくなされたもの
であ勺、防湿性に優れ耐フレーンク2ツク性、カット性
及びヒートシール性を合せ持った包装用途に好適なポリ
エチレン複合フィルムを提供することを目的とする。
The present invention has been made to solve the above-mentioned conventional problems, and provides a polyethylene composite film suitable for packaging applications that has excellent moisture resistance, flake resistance, cuttability, and heat sealability. The purpose is to

問題点を解決するための手段 上記目的を達成する本発明は、架橋度がフィルムの厚さ
方向において内側に低下したポリエチレン延伸フィルム
(以下、単にBOPEフイA/Aという。)の−面に、
140℃における熱収縮率5優未満の積層材(以下、単
に積層材という。)の少くとも1種を積層してなること
全特徴とするポリエチレン複合フィルムを要旨とする。
Means for Solving the Problems The present invention achieves the above-mentioned objects by using a stretched polyethylene film (hereinafter simply referred to as BOPE film A/A) having a polyethylene stretched film (hereinafter simply referred to as BOPE film A/A) whose degree of crosslinking decreases inward in the thickness direction of the film.
The gist of the present invention is a polyethylene composite film that is formed by laminating at least one type of laminate material (hereinafter simply referred to as laminate material) having a heat shrinkage rate of less than 5 at 140°C.

本発明において基材層となるBOPBフィルムは、架橋
度がフィルムの厚さ方向において内側に低下したポリエ
チレンニ軸延伸フィルムである。その架橋度は、ゲル分
率(沸とうp−キシ抽出による不溶部分の割合)で表わ
されるが、内側最低ゲル分率が5%未満で、外側架橋層
ゲル分率に5%以上である。特に内側最低ゲル分率がO
qbで、外側架橋層のゲル分率が20〜70チの範囲で
両側同一に架橋し、フィルムの厚さ方向に架橋層/未架
橋層/架橋層を構成し、各層の構成比が未架橋層:両側
架橋層=1:0.1〜10の範囲であることが好ましい
。又、延伸倍率が一方向に3倍以上、面積倍率9倍以上
に二軸延伸されたものである。上記のBOPKフィルム
は、用途により種類を選択すればよい。
The BOPB film serving as the base layer in the present invention is a biaxially stretched polyethylene film in which the degree of crosslinking decreases inward in the thickness direction of the film. The degree of crosslinking is expressed by the gel fraction (ratio of insoluble portion by boiling p-oxygen extraction), and the lowest inner gel fraction is less than 5% and the outer crosslinked layer gel fraction is 5% or more. In particular, the inner minimum gel fraction is O
qb, the gel fraction of the outer crosslinked layer is in the range of 20 to 70cm, and both sides are crosslinked in the same manner, and the thickness direction of the film constitutes a crosslinked layer/uncrosslinked layer/crosslinked layer, and the composition ratio of each layer is uncrosslinked. Layer: both side crosslinked layer=1: It is preferable that it is in the range of 0.1-10. Further, it is biaxially stretched at a stretching ratio of 3 times or more in one direction and at a stretching ratio of 9 times or more in an area. The type of BOPK film mentioned above may be selected depending on the intended use.

例えば、防湿性、カット性、耐屈曲ピンホール性を必要
とする立場からに、密度Q、935v/α3以上の高密
度ポリエチレンペースが好ましい。特に好ましい物性と
しては、透湿度(y)が下記式で求めた数値以下で、ヘ
イズが5%以下のものである。
For example, high-density polyethylene paste with a density Q of 935v/α3 or more is preferred from the standpoint of requiring moisture resistance, cutability, and bending pinhole resistance. Particularly preferable physical properties include a moisture permeability (y) of not more than a value determined by the following formula, and a haze of 5% or less.

7=17X−棒 〔但し、yU透湿度(17m”/ 24 hrs )、
 Xは延伸フィルムの厚さ(μ)ft表わす。]又、シ
ーラント層として用いる場合には、積層フィルムのカー
ルが少り、低温ヒートシールすることができる線状低密
度ポリエチレンをペースとするものを用いてもよい。
7=17X-rod [However, yU moisture permeability (17m”/24 hrs),
X represents the thickness (μ) ft of the stretched film. ] When used as a sealant layer, a laminated film based on linear low-density polyethylene, which has less curl and can be heat-sealed at low temperatures, may be used.

なお、BOHDフィルムの厚さは、目的用途により適宜
選択されるが、通常10〜50μ程度のものが用いられ
る。
The thickness of the BOHD film is appropriately selected depending on the intended use, but is usually about 10 to 50 μm.

上記のようなりOPBフィルムは、例えば特開昭59−
17432’2号公報、同61− ’74819号公報
等に開示される方法によって製造することができる。例
えば、各種密度のポリエチレン、又防湿性を向上させる
立場からは密度193517cm”以上、メルトインデ
ックス(JよりK6760 、温度190℃、荷重2.
16に9で測定、以下M工)[L5〜202/10分、
ハイロードメルトインデックス(J工8K 6760 
、温度190℃、荷重21.6ゆで測定、以下HLM工
という)/M工 40〜200のポリエチレンを用いた
ものが好ましい。さらにはこれらに水添系石油樹脂を添
加したものが好ましい。な訃、ポリエチレンは混合物で
用いてもよい。このポリエチレンを用いて溶融押出し成
形したシート状又はチューブ状原反を、その厚さ方向に
おいて架橋度が内側に低下するように両側から電子線照
射等によシ架橋し、次いでポリエチレンの融点以下の温
度で二軸方向に延伸する方法があげられる。
The above-mentioned OPB film is, for example, JP-A-59-
It can be manufactured by the methods disclosed in JP-A No. 17432'2, JP-A No. 61-'74819, and the like. For example, from the standpoint of improving moisture resistance, polyethylene of various densities, density 193517 cm or more, melt index (K6760 from J, temperature 190 ° C, load 2.
Measured at 16 to 9, hereafter M-work) [L5 to 202/10 minutes,
High Road Melt Index (J Engineering 8K 6760
, temperature: 190° C., load: 21.6 boiling measurements, hereinafter referred to as HLM work)/M work: Preferably, polyethylene having a rating of 40 to 200 is used. Furthermore, it is preferable to add a hydrogenated petroleum resin to these. However, polyethylene may be used in mixtures. A sheet-like or tube-like original fabric formed by melt extrusion using this polyethylene is cross-linked from both sides by electron beam irradiation, etc. so that the degree of cross-linking decreases toward the inside in the thickness direction, and then An example is a method of biaxially stretching at temperature.

本発明における積層材は、140℃における熱収縮率が
5%未満のものである。140℃における熱収縮率が5
%を越える場合は、EOPICフィルムどうしのヒート
クールにおいて熱収縮が発生し、十分なヒートシールが
できない。積層材の具体例としては、紙、ht箔、セロ
ファン、耐熱性樹脂フィルム等があげられる。紙として
は、塗工紙、両更包装紙、薄葉紙、化粧板用あるいは食
品容器用等の加工原紙があげられる。又、At箔として
は厚さが7〜12μ程度のものが用いられる。又、耐熱
性樹脂フィルムの例としては、ポリエステル、ポリアミ
ド、ポリイミド、ポリパラバン酸、エチレン・ポリビニ
ルアルコール共重合体からなるものがあげられる。これ
ら、耐熱性樹脂フィルムの厚さに通常12〜50μ程度
のものが用いられる。セロファンとしては300番手程
度のものが用いられる。
The laminate material in the present invention has a heat shrinkage rate of less than 5% at 140°C. Heat shrinkage rate at 140℃ is 5
If it exceeds %, thermal shrinkage occurs during heat cooling of the EOPIC films, and sufficient heat sealing cannot be achieved. Specific examples of the laminated material include paper, HT foil, cellophane, heat-resistant resin film, and the like. Examples of the paper include coated paper, double-sided wrapping paper, tissue paper, processed base paper for decorative boards, food containers, and the like. Further, as the At foil, one having a thickness of about 7 to 12 μm is used. Examples of heat-resistant resin films include those made of polyester, polyamide, polyimide, polyparabanic acid, and ethylene/polyvinyl alcohol copolymer. The thickness of these heat-resistant resin films is usually about 12 to 50 microns. Cellophane of approximately 300 count is used.

本発明のポリエチレン複合フイルムハ、基材のEOPB
フィルムと積層材の紙、ムを箔又に耐熱性樹脂フィルム
の少くとも1種との積層フィルムを基本構成とするが、
さらにこの積層フィルムの紙、ht箔又は耐熱性樹脂フ
ィルム面側にシーラント層を設けたものでおってもよい
Polyethylene composite film of the present invention, EOPB as base material
The basic structure is a laminated film consisting of a film and at least one type of laminated material such as paper, a film or a heat-resistant resin film,
Furthermore, a sealant layer may be provided on the paper, HT foil, or heat-resistant resin film side of the laminated film.

シーラントとしては、低密度ポリエチレン、線状低密度
ポリエチレン、エチレン−酢酸ビニル共重合体、エチレ
ン−アクリル酸エチル、アイオノマー、ポリプロピレン
(無延伸のもの)等がめげられる。
Examples of the sealant include low density polyethylene, linear low density polyethylene, ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate, ionomer, polypropylene (unstretched), and the like.

本発明において、基材となるBOPBフィルムに紙、A
t箔又は耐熱性樹脂フィルムを積層する方法とじては、
(1)ウェットラミネート法、(2)ホットメルトラミ
ネート法、(3)ドライラミネート法、(4)押出コー
ティングラミネート法のいずれの方法を用いてもよい。
In the present invention, paper, A
The method of laminating T-foil or heat-resistant resin film is as follows:
Any of the following methods may be used: (1) wet lamination, (2) hot melt lamination, (3) dry lamination, and (4) extrusion coating lamination.

又、積層した複合フィルムの厚さに、目的、用途により
適宜選択されるが、通常に20〜200μ程度でおる。
The thickness of the laminated composite film is appropriately selected depending on the purpose and use, but is usually about 20 to 200 microns.

実施例 以下、本発明を実施例で詳細に説明する。なお、実施例
における試験方法に次の通シである。
EXAMPLES Hereinafter, the present invention will be explained in detail using examples. The following general rules apply to the test methods used in the examples.

(1)透湿度 : JIS Z 0208、温度40℃
、相対湿度90%準拠 (2)ヘイズ :JIS K 6714  準拠(3)
  ヒートシール強度二J工S Z 025B(4)熱
収縮率:140℃の恒温槽(空気)中に、長さ10甑及
び310+mに標線を入れた試験片(巾101×長場3
50日)の2枚(縦方向及び横方向に採取したもの)を
10分間放した後、試験片の加熱前の長さり、  と加
熱後の長さLl からそれぞれの熱収縮率を求めた。
(1) Moisture permeability: JIS Z 0208, temperature 40℃
, relative humidity 90% compliant (2) Haze: JIS K 6714 compliant (3)
Heat sealing strength 2 J engineering S Z 025B (4) Heat shrinkage rate: A test piece with a marked line at length 10 and 310+m (width 101 x length 3
50 days) (taken in the longitudinal and transverse directions) for 10 minutes, the heat shrinkage rate of each test piece was determined from the length before heating, and the length after heating Ll.

熱収縮率”” (L6  Ll / Lo ) X 1
00(5)ゲル分率: A8TM D 2765、A法
準拠(6)  フレキソクランク後のピンホール数:理
学工業(株)製ゲルポフレックステスターを用いて、4
40°角往復/サイクル、40サイクル/分で100回
屈曲させた試験片のピンホール数を数えた。
Heat shrinkage rate "" (L6 Ll / Lo) X 1
00 (5) Gel fraction: A8TM D 2765, compliant with A method (6) Number of pinholes after flexo crank: 4 using Gelpo Flex Tester manufactured by Rigaku Kogyo Co., Ltd.
The number of pinholes in the test piece was counted after it was bent 100 times at 40° angle reciprocation/cycle and 40 cycles/min.

(カ カット性:1型ノツチを入れ手で切って直線にカ
ットできるものを○、その他を×とした。カットの際に
切口がクリアなものを○、僅かにギザギザのものを△、
その他のものを×とした。
(Cutability: Type 1 notches are cut by hand and cut in a straight line as ○, others are marked as ×. Cutting edges that are clear when cut are marked as ○, and those that are slightly jagged are marked as △.
Other items were marked as ×.

(1)高密度ポリエチレン(密度:0.957f1国、
M工:tor/io分、融点:154℃)iTダイ押出
シート成形機により厚さ480μのシート状原反全成形
した。この原反シートラミ子線照射装置(ES’I社製
)を用い、窒素ガス雰囲気下で表裏それぞれに150K
V −’8 mAの条件下で20メガランド照射した。
(1) High-density polyethylene (density: 0.957f1 country,
M process: tor/io min, melting point: 154° C.) A sheet-like original fabric with a thickness of 480 μm was entirely molded using an iT die extrusion sheet molding machine. Using this original sheet laminated beam irradiation equipment (manufactured by ES'I), 150K was applied to each of the front and back sides in a nitrogen gas atmosphere.
20 Megaland irradiation was performed under the condition of V-'8 mA.

この原反シートの照射面およびシートの厚さ方向内部の
架橋度を、厚さ20μの薄いフィルムを24枚重ねて厚
さ480μの試験片とし、同一条件で照射して各々の薄
いフィルムの架橋度を調べたところ、照射面両側の薄い
フィルムの架橋度はゲル分率各々50%、厚さ方向内部
の最低架橋度はゲル分率0%でおった。また、架橋して
いる層および未架橋層の厚さの構成比は、架橋層:未加
橋層:架橋層=1:t75:1であった。
The degree of crosslinking on the irradiated surface of this raw sheet and inside the sheet in the thickness direction was determined by stacking 24 thin films of 20μ thick to form a 480μ thick test piece and irradiating each thin film under the same conditions. When the degree of crosslinking was investigated, the degree of crosslinking of the thin films on both sides of the irradiated surface was 50% gel fraction each, and the lowest degree of crosslinking inside the thickness direction was 0% gel fraction. Further, the composition ratio of the thicknesses of the crosslinked layer and the uncrosslinked layer was crosslinked layer:uncrosslinked layer:crosslinked layer=1:t75:1.

この架橋した原反シー1−’1127℃に加熱した後、
テンター式2軸延伸機で縦方向に4倍、横方向に6倍逐
次延伸して厚さ20μの延伸フィルムを得た。このフィ
ルム(BOHD−1)の特性全表−1rc示した。
After heating this crosslinked raw sheet 1-' to 1127°C,
A stretched film having a thickness of 20 μm was obtained by sequentially stretching 4 times in the machine direction and 6 times in the transverse direction using a tenter type biaxial stretching machine. The complete characteristics table-1rc of this film (BOHD-1) is shown.

伐) 上記のフィルム(BOHD−1)の製造において
電子線照射量を15メガランドとした以外は同様にして
延伸フィルムを得た。このフィルム(BOHD−2)の
特性を表−1に併記した。
A stretched film was obtained in the same manner as in the production of the above film (BOHD-1), except that the electron beam irradiation dose was changed to 15 Megaland. The characteristics of this film (BOHD-2) are also listed in Table-1.

(3)上記のフィルム(BOHD−1)の製造において
、高密度ポリエチレンに代り線状低密度ポリエチレン(
密度Q、9242/譚3、M工zot/1o分)ft用
い電子線照射量ft10Mrad  にして延伸フィル
ムを得た。このフィルム(EOIIL)の特性全表−1
に併記した。
(3) In the production of the above film (BOHD-1), linear low density polyethylene (
A stretched film was obtained by using a density Q of 9242/Tan 3, M engineering zot/10 min) ft, and an electron beam irradiation amount ft 10 Mrad. Full table of characteristics of this film (EOIIL)-1
Also listed.

実施例1〜12、比較例1〜6 基材層: (1) BOHD−1フィルム、(2)EO
HD−2フイルム、(3)BOLLフィルム 積層材:(1)上質紙(50?/rn” ’)、(2)
At箔(9μ)、(3)EvAL−F(15μ、クラレ
社製、商品名)、(4)P、FTPフィルム(12μ)
、(5)セロファン (300番手)、(6) At蒸着ITPフィルム(1
2μ)、(力LDPF! フィルム(30μ)、(8)
 LLDPI フィルム(30μ)、(g) D P 
pフィルム(20μ) 上記積層材(1)〜(6)ハ、140℃における熱収縮
率が5%未満であった。
Examples 1 to 12, Comparative Examples 1 to 6 Base layer: (1) BOHD-1 film, (2) EO
HD-2 film, (3) BOLL film laminated material: (1) High quality paper (50?/rn''), (2)
At foil (9μ), (3) EvAL-F (15μ, manufactured by Kuraray Co., Ltd., trade name), (4) P, FTP film (12μ)
, (5) Cellophane (300 count), (6) At-deposited ITP film (1
2μ), (Power LDPF! Film (30μ), (8)
LLDPI film (30μ), (g) DP
P film (20μ) The above laminate materials (1) to (6) c) had a heat shrinkage rate of less than 5% at 140°C.

上記の基材層及び積層材とを表−2に示す層構成とし、
]!iVA系エマルジョンタイプもしくはアクリル系の
接着剤によるウェットラミネート法、ウレタン系接着剤
によるドライラミネート法又は押出しコーティングラミ
ネート法によりそれぞれを接着積層した。各複合フィル
ムの特性を表−2に示した。
The base material layer and the laminated material have the layer configuration shown in Table 2,
]! Each was adhesively laminated by a wet lamination method using an iVA emulsion type adhesive or an acrylic adhesive, a dry lamination method using a urethane adhesive, or an extrusion coating lamination method. The characteristics of each composite film are shown in Table-2.

発明の効果 本発明の複合フィルムij、BOPKフィルム面どうし
のヒートシールが可能であると共に防湿性、耐フレキン
クランク性及び直線のカット性に優れるものである。又
、各積層材との組合せにより、さらにその機能を高める
ものである。
Effects of the Invention The composite film ij of the present invention allows for heat sealing of the BOPK film surfaces, and has excellent moisture proofing properties, flexing crank resistance, and straight cutability. In addition, its functionality can be further enhanced by combining it with other laminated materials.

例えば、ムを箔との複合化は耐ピンホール性全補い防湿
性をさらに高め、紙との複合化では紙の防湿性を高める
と共にBOPIICフィルムと紙の糊貼り適性をもたせ
る。又、エチレン−ポリビニルアルコール共重合体のよ
うなガスバリヤ−性を有する積層材との複合化では、高
温多湿時のガスバリヤ−性の改善、さらに[P E T
 Pやセロファンとの複合化では、積層フィルムとして
の光学特性を改善する等の機能向上を加えることができ
る。
For example, combining film with foil completely compensates for pinhole resistance and further increases moisture resistance, and combining film with paper improves the moisture resistance of paper and makes it suitable for adhesive bonding between BOPIIC film and paper. In addition, when combined with a laminate material having gas barrier properties such as ethylene-polyvinyl alcohol copolymer, gas barrier properties at high temperatures and high humidity can be improved, and [PET
When combined with P or cellophane, it is possible to add functional improvements such as improving the optical properties of a laminated film.

本発明の複合フィルムに、上記のような優れた特性によ
う各種の包装材料として有でおるが、特にBOPKフィ
ルム面を表面層とするガセット袋や箱材、あるい1jB
OPKフィルム面をシーy層とする袋体等に好適である
Due to the above-mentioned excellent properties, the composite film of the present invention can be used as a variety of packaging materials, but in particular, it can be used in gusseted bags, box materials, or 1JB with the BOPK film surface as the surface layer.
It is suitable for bags etc. in which the OPK film surface is the sea layer.

Claims (1)

【特許請求の範囲】 (1)架橋度がフィルムの厚さ方向において内側に低下
したポリエチレン延伸フィルムの一面に、140℃にお
ける熱収縮率が5%未満である積層材の少くとも1種を
積層してなることを特徴とするポリエチレン複合フィル
ム。 (2)架橋度が、フィルムの厚さ方向において架橋層/
未架橋層/架橋層を構成し、架橋層のゲル分率が20〜
70%、未架橋層のゲル分率が0%で、かつ未架橋層:
架橋層が1: 0.1〜10である特許請求の範囲第1項記載のポリエ
チレン複合フィルム。 (3)積層材が、紙、アルミニウム箔、セロファン及び
耐熱性樹脂フィルムから選択される特許請求の範囲第1
項又は第2項に記載のポリエチレン複合フィルム。
[Scope of Claims] (1) At least one type of laminate material having a heat shrinkage rate of less than 5% at 140°C is laminated on one side of a stretched polyethylene film whose degree of crosslinking decreases inward in the thickness direction of the film. A polyethylene composite film characterized by: (2) The degree of crosslinking is the crosslinked layer /
It constitutes an uncrosslinked layer/crosslinked layer, and the gel fraction of the crosslinked layer is 20~
70%, the gel fraction of the uncrosslinked layer is 0%, and the uncrosslinked layer:
The polyethylene composite film according to claim 1, wherein the crosslinked layer has a ratio of 1:0.1 to 10. (3) Claim 1 in which the laminated material is selected from paper, aluminum foil, cellophane, and heat-resistant resin film.
The polyethylene composite film according to item 1 or 2.
JP62291952A 1987-11-13 1987-11-20 Polyethylene composite film Granted JPH01133737A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP62291952A JPH01133737A (en) 1987-11-20 1987-11-20 Polyethylene composite film
US07/268,498 US5006378A (en) 1987-11-13 1988-11-08 Polyethylene composite film
KR1019880014792A KR910008697B1 (en) 1987-11-13 1988-11-12 Polyethylene Composite Film
EP19880310726 EP0317237A3 (en) 1987-11-13 1988-11-14 A polyethylene composite film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62291952A JPH01133737A (en) 1987-11-20 1987-11-20 Polyethylene composite film

Publications (2)

Publication Number Publication Date
JPH01133737A true JPH01133737A (en) 1989-05-25
JPH0528989B2 JPH0528989B2 (en) 1993-04-28

Family

ID=17775586

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62291952A Granted JPH01133737A (en) 1987-11-13 1987-11-20 Polyethylene composite film

Country Status (1)

Country Link
JP (1) JPH01133737A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016135568A (en) * 2015-01-23 2016-07-28 聡 奥山 Sheet which is hardly contaminated
JP2020158722A (en) * 2019-03-28 2020-10-01 大日本印刷株式会社 Base material, laminate, packaging material, packaging bag and stand pouch
JP2024103688A (en) * 2019-03-28 2024-08-01 大日本印刷株式会社 Laminate, packaging material, packaging bag and stand-up pouch

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59174321A (en) * 1983-03-23 1984-10-02 Toa Nenryo Kogyo Kk Stretched polyethylene film

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59174321A (en) * 1983-03-23 1984-10-02 Toa Nenryo Kogyo Kk Stretched polyethylene film

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016135568A (en) * 2015-01-23 2016-07-28 聡 奥山 Sheet which is hardly contaminated
JP2020158722A (en) * 2019-03-28 2020-10-01 大日本印刷株式会社 Base material, laminate, packaging material, packaging bag and stand pouch
JP2024103688A (en) * 2019-03-28 2024-08-01 大日本印刷株式会社 Laminate, packaging material, packaging bag and stand-up pouch

Also Published As

Publication number Publication date
JPH0528989B2 (en) 1993-04-28

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