JPH10138411A - Composite film - Google Patents

Composite film

Info

Publication number
JPH10138411A
JPH10138411A JP29875096A JP29875096A JPH10138411A JP H10138411 A JPH10138411 A JP H10138411A JP 29875096 A JP29875096 A JP 29875096A JP 29875096 A JP29875096 A JP 29875096A JP H10138411 A JPH10138411 A JP H10138411A
Authority
JP
Japan
Prior art keywords
layer
resin layer
composite film
thickness
vinyl acetate
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
JP29875096A
Other languages
Japanese (ja)
Other versions
JP3586526B2 (en
Inventor
Kazuhide Ishii
和秀 石井
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 JP29875096A priority Critical patent/JP3586526B2/en
Publication of JPH10138411A publication Critical patent/JPH10138411A/en
Application granted granted Critical
Publication of JP3586526B2 publication Critical patent/JP3586526B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Laminated Bodies (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a composite film suitable for obtaining a package which has favorable transparency, whose shrinkage at a molded portion at the time of boiling is small, and whose curling and waviness at a surface seal portion with a lid are small. SOLUTION: This composite film comprises a polypropylene resin layer or a nylon 12 resin layer as a first layer, an adherent resin layer as a second layer, a polyamide resin layer as a third layer, an adherent resin layer as a fourth layer, a low-density polyethylene resin layer or an ethylene vinyl acetate resin layer having a vinyl acetate content of at most 5mol%, or a layer of a blended article whose principal raw materials are composed of these polyethylene resin and ethylene vinyl acetate resin, as a fifth layer, and a straight-chain, low-density polyethylene resin layer whose thickness is 3-15μm, and whose Vicat softening point is in the range of 105-145 deg.C according to JIS K7206, or a polypropylene resin layer, as a sixth layer.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は主として食品の深絞
り包装用底材に使用できる複合フイルムであって、透明
性が良好でかつボイル時の成形部の収縮が少なく、蓋材
とのシール部のカールや波打ちが少ない包装体を得るの
に好適な複合フイルムに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composite film which can be used mainly as a bottom material for deep drawing packaging of foods, has good transparency, has a small shrinkage of a molded portion at the time of boiling, and has a sealing portion with a lid material. The present invention relates to a composite film suitable for obtaining a package having less curl and waving.

【0002】[0002]

【従来の技術】従来、ボイル用の深絞り包装用底材とし
てはナイロン樹脂と直鎖状低密度ポリエチレン樹脂層と
の積層体やナイロン樹脂層とポリプロレン樹脂層との積
層体等が使用されている。
2. Description of the Related Art Conventionally, as a bottom material for deep drawing packaging for boiling, a laminate of a nylon resin and a linear low-density polyethylene resin layer or a laminate of a nylon resin layer and a polypropylene resin layer has been used. I have.

【0003】またハイガスバリアー性のタイプとしては
ナイロン樹脂層/エチレン酢酸ビニル共重合体ケン化物
樹脂層/直鎖状低密度ポリエチレン樹脂層からなる積層
体、ポリプロピレン樹脂層/エチレン酢酸ビニル共重合
体ケン化物樹脂層/ナイロン樹脂層/直鎖状低密度ポリ
エチレン樹脂層からなる積層体及びエチレン酢酸ビニル
共重合体ケン化物樹脂層/ナイロン樹脂層/エチレン酢
酸ビニル共重合体樹脂層との積層体のエチレン酢酸ビニ
ル共重合体ケン化物樹脂層側にポリプロピレンフイルム
をドライラミネートした積層体等が使用されている。
The high gas barrier type is a laminate comprising a nylon resin layer / a saponified ethylene vinyl acetate resin layer / a linear low density polyethylene resin layer, a polypropylene resin layer / an ethylene vinyl acetate copolymer. Of a laminate consisting of a saponified resin layer / nylon resin layer / linear low-density polyethylene resin layer and a laminated body of a saponified ethylene vinyl acetate copolymer resin layer / nylon resin layer / ethylene vinyl acetate copolymer resin layer Laminated products in which a polypropylene film is dry-laminated on the saponified ethylene vinyl acetate copolymer resin layer side are used.

【0004】しかしながらヒートシール層に直鎖状低密
度ポリエチレン樹脂を用いたものではヒートシール時に
直鎖状低密度ポリエチレン樹脂の結晶化によるフイルム
の白化を生じ、シール部の透明性を著しく低下させてし
まうという欠点があった。
However, in the case where the linear low-density polyethylene resin is used for the heat-sealing layer, the film is whitened due to crystallization of the linear low-density polyethylene resin during heat sealing, and the transparency of the sealing portion is remarkably reduced. There was a disadvantage that it would.

【0005】また直鎖状低密度ポリエチレン樹脂自体が
非常に収縮し易い樹脂であり、通常深絞り成形は直鎖状
低密度ポリエチレン樹脂の融点以下で行うため、蓋材を
シールした包装体のシール部のカールや波打ちが防止で
きないという欠点があった。
[0005] In addition, since the linear low-density polyethylene resin itself is a resin that is very easily shrunk, and usually deep drawing is performed at a temperature equal to or lower than the melting point of the linear low-density polyethylene resin, the sealing of the package with the lid material sealed is performed. There is a disadvantage that curling and waving of the part cannot be prevented.

【0006】一方ヒートシール層にエチレン酢酸ビニル
共重合体樹脂を用いたものでは深絞り成形時、成形温度
が高いとシール部側から加熱する熱板に、ヒートシール
層が溶けてとられてしまい、そのため、低温成形せざる
を得なくなり、このため低温成形ではナイロン樹脂等他
の高融点樹脂に成形歪が強く残り、ボイル時に収縮し易
いという欠点があった。さらにナイロン樹脂層とポリプ
ロピレン樹脂層との構成では成形温度が上げられ、収縮
も押えられるが柔らかさ及び耐ピンホール性に問題があ
った。
On the other hand, in the case where the ethylene-vinyl acetate copolymer resin is used for the heat seal layer, if the forming temperature is high at the time of deep drawing, the heat seal layer is melted and taken off by the hot plate heated from the seal portion side. For this reason, low-temperature molding must be performed, so that high-melting-point resin such as nylon resin has strong molding distortion during low-temperature molding, and has a disadvantage that it is easily shrunk during boiling. Further, in the configuration of the nylon resin layer and the polypropylene resin layer, the molding temperature is increased and the shrinkage is suppressed, but there is a problem in softness and pinhole resistance.

【0007】[0007]

【発明が解決しようとする課題】本発明は従来技術の前
記の問題点を解決した新規の複合フイルムを提供するこ
とを目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide a novel composite film which solves the above-mentioned problems of the prior art.

【0008】[0008]

【課題を解決するための手段】前記の目的は以下の手段
によって達成される。
The above object is achieved by the following means.

【0009】すなわち、本発明は、第1層がポリプロピ
レン樹脂層、あるいは12ナイロン樹脂層、第2層が接
着樹脂層、第3層がポリアミド樹脂層、第4層が接着樹
脂層からなり、第5層が低密度ポリエチレン樹脂層また
は酢酸ビニル含量5モル%以下のエチレン酢酸ビニル樹
脂層、あるいはそれらを主原料とするブレンド物層であ
り、第6層が厚みが3〜15μmでJISK7206に
よるビカット軟化点が105℃〜145℃の範囲の直鎖
状低密度ポリエチレン樹脂層またはポリプロピレン樹脂
層からなることを特徴とする複合フイルムを提案するも
のであり、また本発明は前記の複合フイルムのポリアミ
ド樹脂層に隣接、または接着樹脂層を介して、エチレン
酢酸ビニル共重合体ケン化物樹脂層を設けたことを特徴
とする複合フイルム提案するものである。さらに、本発
明は前記第1層のポリプロピレン樹脂層を共押出法によ
り積層した共押出複合フイルム表面にドライラミネート
してなることを含む。
That is, according to the present invention, the first layer comprises a polypropylene resin layer or a 12 nylon resin layer, the second layer comprises an adhesive resin layer, the third layer comprises a polyamide resin layer, and the fourth layer comprises an adhesive resin layer. Five layers are a low-density polyethylene resin layer, an ethylene vinyl acetate resin layer having a vinyl acetate content of 5 mol% or less, or a blend layer containing them as a main material, and a sixth layer is 3 to 15 μm thick and is Vicat softened according to JIS K7206. The present invention proposes a composite film comprising a linear low-density polyethylene resin layer or a polypropylene resin layer having a temperature in the range of 105 ° C. to 145 ° C., and the present invention provides a polyamide resin layer of the composite film. Characterized in that a saponified ethylene-vinyl acetate copolymer resin layer is provided adjacent to or via an adhesive resin layer. It is intended to propose. Further, the present invention includes that the first polypropylene resin layer is dry-laminated on the surface of a co-extruded composite film obtained by laminating by a co-extrusion method.

【0010】[0010]

【発明の実施の形態】以下、本発明を更に詳細に説明す
る。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described below in more detail.

【0011】本発明の請求項1の複合フイルムの構成が
第1層はポリプロピレン樹脂層(以下PPという)ある
いは、12ナイロン樹脂層(以下12Nyという)であ
り、その厚みは5〜70μmの範囲が好ましい。また第
2層は接着樹脂層、第3層はポリアミド樹脂層(以下N
yという)、第4層は接着樹脂層、第5層は低密度ポリ
エチレン樹脂層(以下LDPEという)あるいは酢酸ビ
ニル含量が5モル%以下のエチレン酢酸ビニル樹脂層
(以下EVAという)あるいはそれらを主原料とするブ
レンド物の層であり、第6層のシール層は厚みが3〜1
5μmでJISK7206によるビカット軟化点が10
5℃〜145℃の範囲の直鎖状低密度ポリエチレン樹脂
層(以下LLDPEという)またはPPからなる複合フ
イルムである。シール層の厚みが3μm未満ではヒート
シール時に熱板にとられ易く、15μmを越えるとシー
ル時の結晶化による白化を低く押えることができないと
いう問題がある。第2層及び第4層の接着樹脂としては
酸変性ポリオレフィン樹脂等が挙げられ厚みは3〜20
μmの範囲が好ましい。また第3層のNyとしては6ナ
イロン、6−66ナイロン、12ナイロン、6−12ナ
イロン等が挙げられるが6ナイロンが成形品の収縮応力
は小さく、ボイル時の収縮がより押えられるのでより好
ましい。
In the composite film according to the first aspect of the present invention, the first layer is a polypropylene resin layer (hereinafter referred to as PP) or a 12 nylon resin layer (hereinafter referred to as 12 Ny), and the thickness thereof is in the range of 5 to 70 μm. preferable. The second layer is an adhesive resin layer, and the third layer is a polyamide resin layer (hereinafter N
y), the fourth layer is an adhesive resin layer, and the fifth layer is a low-density polyethylene resin layer (hereinafter referred to as LDPE) or an ethylene vinyl acetate resin layer having a vinyl acetate content of 5 mol% or less (hereinafter referred to as EVA) or a combination thereof. This is a layer of a blend as a raw material, and the sixth sealing layer has a thickness of 3 to 1
Vicat softening point according to JIS K7206 is 10 at 5 μm
A composite film comprising a linear low-density polyethylene resin layer (hereinafter referred to as LLDPE) or PP in the range of 5 ° C to 145 ° C. If the thickness of the sealing layer is less than 3 μm, it tends to be formed on a hot plate during heat sealing, and if it exceeds 15 μm, there is a problem that whitening due to crystallization during sealing cannot be suppressed low. Examples of the adhesive resin for the second and fourth layers include an acid-modified polyolefin resin and the like.
The range of μm is preferred. As the Ny of the third layer, 6 nylon, 6-66 nylon, 12 nylon, 6-12 nylon and the like can be mentioned, but 6 nylon is more preferable because the shrinkage stress of the molded product is small and the shrinkage during boiling is suppressed more. .

【0012】上記Nyの厚みは5〜70μmの範囲が好
ましい。LDPEもしくはEVAもしくはそれらを主原
料とするブレンド物からなる第5層の厚みは15〜15
0μmの範囲が好ましい。EVAの酢酸ビニル含量は0
〜5モル%の範囲が好ましい。含量5モル%を越えると
収縮率大きくなりボイル時に収縮し易いという問題があ
る。
The thickness of Ny is preferably in the range of 5 to 70 μm. The thickness of the fifth layer made of LDPE or EVA or a blend containing them as a main raw material is 15 to 15
A range of 0 μm is preferred. EVA has a vinyl acetate content of 0
The range of about 5 mol% is preferred. If the content exceeds 5 mol%, there is a problem that the shrinkage rate increases and shrinkage easily occurs during boiling.

【0013】またLDPE、EVAを主原料とするブレ
ンド物の割合は特に制限されず、適宜収縮性を考慮して
決めればよい。
The ratio of the blend mainly composed of LDPE and EVA is not particularly limited, and may be determined in consideration of shrinkage.

【0014】第6層のシール層はJISK7206によ
るビカット軟化点が105℃〜145℃の範囲とするこ
とが肝要である。
It is important that the sixth sealing layer has a Vicat softening point in the range of 105 ° C. to 145 ° C. according to JIS K7206.

【0015】ビカット軟化点が105℃未満ではNy及
び他の層の成形歪を小さく押えることができず、ボイル
時の成形部の収縮を小さくすることができず、好ましく
なく145℃を越えるとヒートシール性悪くなり好まし
くない。
If the Vicat softening point is lower than 105 ° C., the molding distortion of Ny and other layers cannot be suppressed small, and the shrinkage of the molded portion during boiling cannot be reduced. It is not preferable because the sealing property deteriorates.

【0016】第6層のシール層のPPはランダム共重合
タイプのPPを用いる方がより成形温度を高くすること
ができ好ましいが隣接する第5層との層間接着強度が不
充分となる場合は第5層の樹脂にポリエチレンとα−オ
レフィンの共重合体で密度0.9以下の低結晶性樹脂を
添加することにより層間強度を向上を図ることができて
好ましい。
As the PP for the sixth sealing layer, it is preferable to use a random copolymerization type PP because the molding temperature can be increased more. However, if the interlayer adhesion strength with the adjacent fifth layer becomes insufficient, It is preferable to add a low-crystalline resin of a copolymer of polyethylene and α-olefin having a density of 0.9 or less to the resin of the fifth layer because the interlayer strength can be improved.

【0017】第1の外層のPPはホモポリマーの方が収
縮応力が小さく良好であるが光沢、透明性の良いランダ
ム共重合タイプのPPを用いることもできる。その場合
はPPの厚みを厚めにする方が収縮は小さくなり良好で
ある。
As the PP of the first outer layer, a homopolymer is preferable because it has a small shrinkage stress and is good, but a random copolymer type PP having good gloss and transparency can be used. In that case, the larger the thickness of the PP, the smaller the shrinkage, which is better.

【0018】また請求項2の複合フイルムはガスバリア
ー性を付与するために上記層構成でNyに隣接または接
着樹脂層を介してエチレン酢酸ビニル共重合体ケン化物
樹脂層(以下EVOHという)を設けたものであり、食
品等の長期保存を可能にできる。さらに請求項3の複合
フイルムは、上述した第1層のPPをドライラミネート
により他層の共押出複合フイルムに積層したものであ
り、ボイル時の収縮を低減し易いという利点がある。
The composite film according to claim 2 is provided with a saponified ethylene vinyl acetate copolymer resin layer (hereinafter referred to as EVOH) adjacent to Ny or with an adhesive resin layer interposed therebetween in order to impart gas barrier properties. It is possible to store foods and the like for a long time. Further, the composite film of the third aspect is obtained by laminating the above-mentioned first layer of PP on a co-extruded composite film of another layer by dry lamination, and has an advantage that shrinkage during boiling is easily reduced.

【0019】[0019]

【実施例】以下、本発明を実施例により具体的に説明す
る。
The present invention will be described below in more detail with reference to examples.

【0020】実施例1 層構成が下記6層からなる複合フイルムを共押出して共
押出複合フイルムを得た。PP(厚み40μm)/接着
樹脂(10μm)/Ny(厚み30μm)/接着樹脂
(厚み10μm)/LDPE(厚み50μm)/LLD
PE(厚み10μm)なお、外層のPPはエチレンとの
ランダムコーポリマーであり、LLDPEのビカット軟
化点は110℃であった。得られた共押出複合フイルム
を表1に示す成形可能な上限温度(熱板とのとられが発
生しない上限温度)で大森機械工業社製深絞り包装機F
V6300を使用して1.5秒間加熱して成形し、得ら
れた底材に内容物を充填した後、蓋材を面シールし、包
装体を得、包装体をボイル条件98℃×20分でボイル
し、ボイル時の収縮状態及び面シール部の透明性及び耐
ピンホール性を評価した。結果を表1に示す。
Example 1 A composite film composed of the following six layers was co-extruded to obtain a co-extruded composite film. PP (thickness 40 μm) / adhesive resin (10 μm) / Ny (thickness 30 μm) / adhesive resin (thickness 10 μm) / LDPE (thickness 50 μm) / LLD
PE (thickness: 10 μm) The PP of the outer layer was a random copolymer with ethylene, and the Vicat softening point of LLDPE was 110 ° C. The obtained co-extruded composite film was subjected to molding at the maximum molding temperature shown in Table 1 (the maximum temperature at which the film was not removed from the hot plate), and the deep drawing packaging machine F manufactured by Omori Machinery Co., Ltd.
After heating and molding for 1.5 seconds using V6300 and filling the obtained bottom material with the contents, the lid material was face-sealed to obtain a package, and the package was boiled at 98 ° C for 20 minutes. Then, the shrinkage state at the time of boiling, the transparency of the face seal portion and the pinhole resistance were evaluated. Table 1 shows the results.

【0021】なお、蓋材は延伸NyとEVAのドライラ
ミネート積層体を用いた。
The lid was a dry laminate of stretched Ny and EVA.

【0022】評価法 ・ボイル時の収縮状態 ボイル時に波打ち傾向の全くないものを〇とし、収縮し
て波打ち気味のものを△とし、収縮して波打ちを発生し
たものを×とした。 ・面シール部の透明性 ヒートシール部に白化の全くなかったものを〇とし、白
化の小さいものを△とし、白化したものを×とした。 ・耐ピンホール性 ボイルによりピンホールが全くないものを〇とし、ピン
ホールを発生したものを×とした。
Evaluation method-Shrinking state at the time of boiling Boiled with no tendency to undulate at the time of boiling, 〇 when shrunk and slightly wavy, and X when shrunk and undulated. -Transparency of the face seal portion The heat seal portion having no whitening was marked with 〇, the one with little whitening was marked with △, and the whitened portion was marked with x. -Pinhole resistance The pinholes with no pinholes due to boiling were marked with "〇" and those with pinholes were marked with "x".

【0023】実施例2 層構成が下記7層からなる複合フイルムを共押出して共
押出複合フイルムを得た。
Example 2 A composite film having the following seven layers was co-extruded to obtain a co-extruded composite film.

【0024】PP(厚み40μm)/接着樹脂(厚み1
0μm)/Ny(厚み30μm)/EVOH(厚み10
μm)/接着樹脂(厚み10μm)/LDPE(厚み4
0μm)/LLDPE(厚み10μm) なお、PPとLLDPEは実施例1と同様のものを用い
た。得られた共押出複合フイルムを実施例1と同様に評
価した。結果を表1に示す。
PP (thickness: 40 μm) / adhesive resin (thickness: 1)
0 μm) / Ny (thickness 30 μm) / EVOH (thickness 10
μm) / adhesive resin (thickness 10 μm) / LDPE (thickness 4
0 μm) / LLDPE (thickness: 10 μm) The same PP and LLDPE as in Example 1 were used. The obtained co-extruded composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0025】実施例3 層構成が下記5層からなる複合フイルムを共押出して共
押出複合フイルムを得た。
Example 3 A composite film having the following five layers was co-extruded to obtain a co-extruded composite film.

【0026】EVOH(厚み20μm)/Ny(厚み2
0μm)/接着樹脂(厚み10μm)/EVA(厚み4
0μm)/LLDPE(厚み10μm) 上記共押出複合フイルムのEVOH側に厚み50μmの
PPをドライラミネートして6層の複合フイルムを得
た。
EVOH (thickness 20 μm) / Ny (thickness 2
0 μm) / adhesive resin (thickness 10 μm) / EVA (thickness 4
0 μm) / LLDPE (thickness: 10 μm) PP having a thickness of 50 μm was dry-laminated on the EVOH side of the co-extruded composite film to obtain a six-layer composite film.

【0027】なお、PPとLLDPEは実施例1と同様
のものを用いた。
The same PP and LLDPE as those used in Example 1 were used.

【0028】得られた複合フイルムを実施例1と同様に
評価した。結果を表1に示す。
The obtained composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0029】実施例4 層構成が下記6層からなる複合フイルムを共押出し、共
押出複合フイルムを得た。
Example 4 A composite film having the following six layers was co-extruded to obtain a co-extruded composite film.

【0030】PP1 (厚み40μm)/接着樹脂(厚み
10μm)/Ny(厚み30μm)/接着樹脂(厚み1
0μm)/LL(厚み50μm)/PP2 (厚み10μ
m) なお、PP2 としてエチレンとのランダムコーポリマー
のPPを、PP1 としてホモポリマーのPPを用いた。
PP 1 (thickness 40 μm) / adhesive resin (thickness 10 μm) / Ny (thickness 30 μm) / adhesive resin (thickness 1
0 μm) / LL (thickness 50 μm) / PP 2 (thickness 10 μm)
m) In addition, the PP random copolymer of ethylene as PP 2, using PP homopolymer as PP 1.

【0031】得られた共押出複合フイルムを実施例1と
同様に評価した。結果を表1に示す。
The obtained co-extruded composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0032】実施例5 層構成が下記7層からなる複合フイルムを共押出し、本
発明の複合フイルムを得た。
Example 5 A composite film having the following seven layers was co-extruded to obtain a composite film of the present invention.

【0033】12Ny(厚み10μm)/接着樹脂(厚
み10μm)/Ny(厚み30μm)/EVOH(厚み
10μm)/接着樹脂(厚み10μm)/EVA(厚み
70μm)/LLDPE(厚み10μm) なお、LLDPEは実施例1と同様のものを用いた。E
VAの酢酸ビニル含量は3モル%。
12 Ny (thickness 10 μm) / adhesive resin (thickness 10 μm) / Ny (thickness 30 μm) / EVOH (thickness 10 μm) / adhesive resin (thickness 10 μm) / EVA (thickness 70 μm) / LLDPE (thickness 10 μm) The same one as in Example 1 was used. E
VA has a vinyl acetate content of 3 mol%.

【0034】得られた共押出複合フイルムを実施例1と
同様に評価した。結果を表1に示す。
The obtained co-extruded composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0035】比較例1 層構成が下記5層からなる複合フイルムを共押出し、共
押出複合フイルムを得た。
Comparative Example 1 A composite film having the following five layers was co-extruded to obtain a co-extruded composite film.

【0036】PP(厚み40μm)/接着樹脂(厚み1
0μm)/Ny(厚み30μm)/接着樹脂(厚み10
μm)/LLDPE(厚み60μm) なお、LLDPEは実施例1と同様のものを用いた。
PP (thickness: 40 μm) / adhesive resin (thickness: 1)
0 μm) / Ny (thickness 30 μm) / adhesive resin (thickness 10
μm) / LLDPE (thickness: 60 μm) The same LLDPE as in Example 1 was used.

【0037】得られた複合フイルムを実施例1と同様に
評価した。結果を表1に示す。
The obtained composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0038】比較例2 層構成が下記6層からなる複合フイルムを共押出し、共
押出複合フイルムを得た。
Comparative Example 2 A composite film having the following six layers was coextruded to obtain a coextruded composite film.

【0039】PP(厚み40μm)/接着樹脂(厚み1
0μm)/Ny(厚み30μm)/接着樹脂(厚み10
μm)/LDPE(厚み40μm)/LLDPE(厚み
20μm) なお、LLDPEは実施例1と同様のものを用いた。
PP (thickness: 40 μm) / adhesive resin (thickness: 1)
0 μm) / Ny (thickness 30 μm) / adhesive resin (thickness 10
μm) / LDPE (thickness: 40 μm) / LLDPE (thickness: 20 μm) The same LLDPE as in Example 1 was used.

【0040】得られた複合フイルムを実施例1と同様に
評価した。結果を表1に示す。
The obtained composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0041】比較例3 層構成が下記6層の複合フイルムを共押出し、複合フイ
ルムを得た。
Comparative Example 3 A composite film having the following six layers was co-extruded to obtain a composite film.

【0042】PP(厚み40μm)/接着樹脂(厚み1
0μm)/Ny(厚み30μm)/接着樹脂(厚み10
μm)/LDPE(厚み50μm)/LLDPE(厚み
10μm) なお、LLDPEはビカット軟化点100℃のものを用
いた。
PP (thickness: 40 μm) / adhesive resin (thickness: 1)
0 μm) / Ny (thickness 30 μm) / adhesive resin (thickness 10
μm) / LDPE (thickness 50 μm) / LLDPE (thickness 10 μm) The LLDPE used had a Vicat softening point of 100 ° C.

【0043】得られた複合フイルムを実施例1と同様に
評価した。結果を表1に示す。
The obtained composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0044】比較例4 層構成が下記5層からなる複合フイルムを共押出して複
合フイルムを得た。
Comparative Example 4 A composite film having the following five layers was coextruded to obtain a composite film.

【0045】EVOH(厚み20μm)/Ny(厚み2
0μm)/接着樹脂(厚み10μm)/EVA(厚み4
0μm)/LLDPE(厚み10μm) なお、LLDPEは比較例3と同様のものを用いた。E
VAの酢酸ビニル含量は3モル%。
EVOH (thickness 20 μm) / Ny (thickness 2
0 μm) / adhesive resin (thickness 10 μm) / EVA (thickness 4
0 μm) / LLDPE (thickness: 10 μm) The same LLDPE as in Comparative Example 3 was used. E
VA has a vinyl acetate content of 3 mol%.

【0046】前記の共押出複合フイルムのEVOH側に
厚み50μmのPPをドライラミネートして複合フイル
ムを得た。
A 50 μm-thick PP was dry-laminated on the EVOH side of the co-extruded composite film to obtain a composite film.

【0047】得られた複合フイルムを実施例1と同様に
評価した。その結果を表1に示す。 比較例5 層構成が下記3層からなる複合フイルムを共押出し、複
合フイルムを得た。
The obtained composite film was evaluated in the same manner as in Example 1. Table 1 shows the results. Comparative Example 5 A composite film having the following three layers was co-extruded to obtain a composite film.

【0048】Ny(厚み50μm)/接着樹脂(厚み1
0μm)/PP(厚み90μm)得られた複合フイルム
を実施例1と同様に評価した。その結果を表1に示す。
Ny (thickness: 50 μm) / adhesive resin (thickness: 1)
0 μm) / PP (thickness: 90 μm) The obtained composite film was evaluated in the same manner as in Example 1. Table 1 shows the results.

【0049】表1から本発明の複合フイルムを用いた包
装体である実施例1乃至5はいずれもボイル時に収縮が
発生せず、また面シール部の透明性が良好であり、耐ピ
ンホール性も良好であることが判る。これに対して、シ
ール層の厚みが厚すぎる比較例1、2では面シール部の
透明性に劣り、シール層のLLDPEのビカット軟化点
が低い比較例3、4ではボイル時に収縮して波打ちが発
生し、問題があることが判る。さらに比較例5では、ボ
イル時の収縮はないがシール部の白化や耐ピンホール性
に劣ることが判る。
From Table 1, it can be seen that Examples 1 to 5 which are the packages using the composite film of the present invention do not shrink when boiled, have good transparency of the face seal portion, and have a pinhole resistance. It can also be seen that it is good. On the other hand, in Comparative Examples 1 and 2 in which the thickness of the seal layer is too thick, the transparency of the face seal portion is inferior, and in Comparative Examples 3 and 4 in which the Vicat softening point of the LLDPE of the seal layer is low, shrinkage occurs at the time of boiling and undulation occurs. Occurred and found to be problematic. Further, in Comparative Example 5, although there is no shrinkage at the time of boiling, it is found that the whitening of the seal portion and the pinhole resistance are inferior.

【0050】[0050]

【表1】 [Table 1]

【0051】[0051]

【発明の効果】本発明によれば透明性が良好でかつボイ
ル時の成形部の収縮が少なく、蓋材とのシール部のカー
ルや波打ちが少ない包装体を得るのに好適な複合フイル
ムを提供できる。
According to the present invention, there is provided a composite film which is suitable for obtaining a package having good transparency, little shrinkage of the molded part at the time of boiling, and little curling or waving of the sealing part with the lid material. it can.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 第1層がポリプロピレン樹脂層、あるい
は12ナイロン樹脂層、第2層が接着樹脂層、第3層が
ポリアミド樹脂層、第4層が接着樹脂層からなり、第5
層が低密度ポリエチレン樹脂層または酢酸ビニル含量5
モル%以下のエチレン酢酸ビニル樹脂層、あるいはそれ
らを主原料とするブレンド物層であり、第6層が厚みが
3〜15μmでJISK7206によるビカット軟化点
が105℃〜145℃の範囲の直鎖状低密度ポリエチレ
ン樹脂層またはポリプロピレン樹脂層からなることを特
徴とする複合フイルム。
A first layer comprising a polypropylene resin layer or a 12 nylon resin layer; a second layer comprising an adhesive resin layer; a third layer comprising a polyamide resin layer; a fourth layer comprising an adhesive resin layer;
The layer is a low density polyethylene resin layer or vinyl acetate content 5
Mole% or less of an ethylene vinyl acetate resin layer or a blend layer containing them as a main raw material, wherein the sixth layer has a thickness of 3 to 15 μm and a linear linear shape having a Vicat softening point according to JIS K7206 of 105 ° C. to 145 ° C. A composite film comprising a low-density polyethylene resin layer or a polypropylene resin layer.
【請求項2】 請求項1に記載の複合フイルムのポリア
ミド樹脂層に隣接、または接着樹脂層を介して、エチレ
ン酢酸ビニル共重合体ケン化物樹脂層を設けたことを特
徴とする複合フイルム。
2. A composite film according to claim 1, wherein a saponified ethylene vinyl acetate copolymer resin layer is provided adjacent to the polyamide resin layer of the composite film or via an adhesive resin layer.
【請求項3】 第1層のポリプロピレン樹脂層を共押出
法により積層した共押出複合フイルム表面にドライラミ
ネートしてなる請求項1または請求項2記載の複合フイ
ルム。
3. The composite film according to claim 1, wherein the first polypropylene resin layer is dry-laminated on the surface of a co-extruded composite film obtained by laminating by a co-extrusion method.
JP29875096A 1996-11-11 1996-11-11 Composite film Expired - Lifetime JP3586526B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29875096A JP3586526B2 (en) 1996-11-11 1996-11-11 Composite film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29875096A JP3586526B2 (en) 1996-11-11 1996-11-11 Composite film

Publications (2)

Publication Number Publication Date
JPH10138411A true JPH10138411A (en) 1998-05-26
JP3586526B2 JP3586526B2 (en) 2004-11-10

Family

ID=17863759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29875096A Expired - Lifetime JP3586526B2 (en) 1996-11-11 1996-11-11 Composite film

Country Status (1)

Country Link
JP (1) JP3586526B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11115128A (en) * 1997-10-21 1999-04-27 Mitsubishi Plastics Ind Ltd Easily peelable composite film
JP2000296587A (en) * 1999-02-12 2000-10-24 Sumitomo Bakelite Co Ltd Laminate and sealed vessel
JP2013086512A (en) * 2011-10-14 2013-05-13 Evonik Industries Ag Use of multilayered sheet, having oxygen permeable barrier, for photoelectromotive force module

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11115128A (en) * 1997-10-21 1999-04-27 Mitsubishi Plastics Ind Ltd Easily peelable composite film
JP2000296587A (en) * 1999-02-12 2000-10-24 Sumitomo Bakelite Co Ltd Laminate and sealed vessel
JP2013086512A (en) * 2011-10-14 2013-05-13 Evonik Industries Ag Use of multilayered sheet, having oxygen permeable barrier, for photoelectromotive force module

Also Published As

Publication number Publication date
JP3586526B2 (en) 2004-11-10

Similar Documents

Publication Publication Date Title
EP1377450B1 (en) Coextruded retortable multilayer film
EP0476836B2 (en) Biaxially oriented laminated film
JP2615191B2 (en) Blocking stretch film
JPH11500374A (en) Juice-carton structure with long life and its construction method
AU2002248623A1 (en) Coextruded retortable multilayer film
EP1137534B1 (en) Multilayer heat shrinkable film
US5318824A (en) Packaging structure
CN114423610A (en) Packaging body
JP3586526B2 (en) Composite film
US4973375A (en) Process for producing a composite sheet
JP2003145699A (en) Coextrusion composite film for deep draw packaging, and deep draw package
JP2002103542A (en) Composite film for bottom material of boiling treatment
JP3795205B2 (en) Easy-open composite film
JP4636479B2 (en) Polyolefin multilayer film and package
JPH07256836A (en) Composite film for retort and deep-draw package
JPS6027000Y2 (en) Composite film for deep drawing
JP3789552B2 (en) Bag body for bag in box
JP3573659B2 (en) Multilayer sheets and containers
JP3294762B2 (en) Sealed container
JP3808143B2 (en) Co-extrusion composite film
JP3366735B2 (en) Heat shrinkable composite film
JPH1076616A (en) Co-extruded composite film
JP3790028B2 (en) Deep drawn package
JP3826969B2 (en) Manufacturing method of molded container
JP4330240B2 (en) Multi-layer film and heat sealable film

Legal Events

Date Code Title Description
A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20040330

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20040421

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20040615

RD03 Notification of appointment of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7423

Effective date: 20040615

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20040721

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20040809

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080813

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090813

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100813

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110813

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110813

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120813

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130813

Year of fee payment: 9

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

EXPY Cancellation because of completion of term