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JP2003165189A - Composite film - Google Patents

Composite film

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Publication number
JP2003165189A
JP2003165189A JP2001366051A JP2001366051A JP2003165189A JP 2003165189 A JP2003165189 A JP 2003165189A JP 2001366051 A JP2001366051 A JP 2001366051A JP 2001366051 A JP2001366051 A JP 2001366051A JP 2003165189 A JP2003165189 A JP 2003165189A
Authority
JP
Japan
Prior art keywords
layer
film
thickness
composite film
resin layer
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
JP2001366051A
Other languages
Japanese (ja)
Other versions
JP3904906B2 (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 Chemical Corp
Original Assignee
Mitsubishi Plastics Industries 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 Mitsubishi Plastics Industries Ltd filed Critical Mitsubishi Plastics Industries Ltd
Priority to JP2001366051A priority Critical patent/JP3904906B2/en
Publication of JP2003165189A publication Critical patent/JP2003165189A/en
Application granted granted Critical
Publication of JP3904906B2 publication Critical patent/JP3904906B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

(57)【要約】 【課題】 成形性、シール性、及びイージーピール性が
良好で、座薬包装用に好適に使用できる複合フィルムを
提供する。 【解決手段】 少なくとも外層よりポリブチレンテレフ
タレート樹脂層、非晶性ポリエステル樹脂層、凝集破壊
層、シール層の順に積層され、ポリブチレンテレフタレ
ート樹脂層の厚さが全体の1〜20%、非晶性ポリエス
テル樹脂層の厚さが全体の30〜90%であることを特
徴とする複合フィルム。
PROBLEM TO BE SOLVED: To provide a composite film which has good moldability, sealability and easy peelability and can be suitably used for suppository packaging. SOLUTION: A polybutylene terephthalate resin layer, an amorphous polyester resin layer, a cohesion failure layer, and a seal layer are laminated in this order from at least an outer layer, and the thickness of the polybutylene terephthalate resin layer is 1 to 20% of the whole, A composite film, wherein the thickness of the polyester resin layer is 30 to 90% of the whole.

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】本発明は主に成形性、シール
性、及びイージーピール性が良好で、座薬包装用に好適
に使用できる複合フィルムに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composite film having good moldability, sealing property and easy peeling property, which can be suitably used for suppository packaging.

【0002】[0002]

【従来の技術】従来、座薬包装用フィルムには、成形性
およびシール時の耐熱性が良好なポリ塩化ビニル樹脂
(PVC)フィルムを基材とするものが使用されてい
た。主にはPVCフィルムにポリエチレン(PE)樹脂
を押出ラミネートし、座薬を包装後そのPVCフィルム
とPE層の層間で剥離させ開封させるというものであっ
た。
2. Description of the Related Art Conventionally, as a suppository packaging film, a film made of a polyvinyl chloride resin (PVC) film, which is excellent in moldability and heat resistance during sealing, has been used. Mainly, a polyethylene (PE) resin was extrusion-laminated on a PVC film, a suppository was packaged, and then peeled between the PVC film and the PE layer and opened.

【0003】[0003]

【発明が解決しようとする課題】従来使用されていた上
記のPVC構成品は、塩素を含む化合物として廃棄物の
問題等により敬遠されてきた。しかし成形性、腰、シー
ル時の耐熱性の点でPVC代替となる基材がなかった。
また生産性向上のため共押出のみで一度に生産する方式
を取った場合、イージーピールによる開封時の膜残り等
の問題があった。座薬用包装機は一般に成形とシール工
程が一体構造となっており、成形とシール工程を同じ温
度で行う必要となるため、基材の選択が非常に難しいも
のとなっている。基材にPVC以外の樹脂を使用した場
合、成形性は良好であるがシール時の耐熱性が不十分で
シールの熱板にフィルムが融着してしまう現象すなわち
熱板取られ現象を起こすトラブルや、シール時の耐熱性
は良好であるが、成形性が悪くなってしまうという問題
があった。
The above-mentioned PVC components that have been used conventionally have been shunned as a compound containing chlorine due to the problem of waste. However, there is no base material that can substitute for PVC in terms of moldability, stiffness, and heat resistance during sealing.
Further, when a method of producing only one time by co-extrusion is adopted for improving productivity, there is a problem such as a film remaining at the time of opening due to easy peel. Since the packaging machine for suppositories generally has an integral structure for the molding and sealing steps, and the molding and sealing steps must be performed at the same temperature, it is very difficult to select the base material. When a resin other than PVC is used as the base material, the moldability is good, but the heat resistance at the time of sealing is insufficient and the phenomenon that the film is fused to the hot plate of the seal, that is, the problem of the hot plate being removed, Although the heat resistance at the time of sealing is good, there is a problem that the moldability is deteriorated.

【0004】[0004]

【課題を解決するための手段】本発明は上記問題点を解
消できる複合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、少なくとも外層よりポリブチレンテ
レフタレート樹脂層、非晶性ポリエステル樹脂層、凝集
破壊層、シール層の順に積層され、ポリブチレンテレフ
タレート樹脂層の厚さが全体の1〜20%、非晶性ポリ
エステル樹脂層の厚さが全体の30〜90%であること
を特徴とする複合フィルムにある。
DISCLOSURE OF THE INVENTION The present invention has found a composite film capable of solving the above problems, and its gist is to provide a polybutylene terephthalate resin layer and an amorphous polyester resin layer at least from the outer layer. The cohesive failure layer and the seal layer are laminated in this order, and the polybutylene terephthalate resin layer has a thickness of 1 to 20% of the total thickness, and the amorphous polyester resin layer has a thickness of 30 to 90% of the total. It is in a composite film.

【0005】[0005]

【発明の実施の形態】以下、本発明を詳細に説明する。
最外層のポリブチレンテレフタレート樹脂(以下「PB
T」と略記する)層の厚さは全体の1〜20%である必
要があるが、PBTは熱板取られを防止するために配し
ているので表面層に僅かな厚みがあれば良く、成形性を
阻害しない範囲の厚さとすればよく、好ましくは、PB
T層の厚さは全体の1〜10%、更に好ましくは1〜5
%の範囲である。1%未満では熱板取られ防止効果の安
定性に問題があり、20%を越えると成形性を阻害する
可能性が大きいという問題がある。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.
The outermost polybutylene terephthalate resin (hereinafter "PB
The thickness of the layer (abbreviated as "T") needs to be 1 to 20% of the whole, but since PBT is arranged to prevent hot plate removal, it suffices if the surface layer has a slight thickness. The thickness may be within a range that does not impair the moldability, and preferably PB
The thickness of the T layer is 1 to 10% of the whole, more preferably 1 to 5
% Range. If it is less than 1%, there is a problem in the stability of the hot plate removal prevention effect, and if it exceeds 20%, there is a large possibility that the moldability is impaired.

【0006】上記PBT層に隣接する非晶性ポリエステ
ル樹脂層に用いるポリエステル樹脂はホモタイプ、共重
合タイプ樹脂に限定されないが、成形性が要求されるた
め結晶化度を極力低く抑える必要がある。特に結晶性の
高いホモタイプ樹脂の場合、製膜後急冷して無定形状態
とする必要がある。また酸成分としてテレフタル酸、ア
ルコール成分としてエチレングリコール、1,4−シク
ロヘキサンジメタノールを使用した共重合ポリエステル
樹脂である、イーストマンケミカル社製「PETG」が
非晶性であり好適に使用できる。ここで非晶性ポリエス
テル樹脂層の厚さは全体の30〜90%であることが必
要であるが、これは成形性の悪い外層PBTの成形性を
カバーするためであり、30%未満では成形性が不十分
となる可能性が極めて高く、また腰も低くなるため好ま
しくない。逆に80%を越えるとシール層、イージーピ
ール層並びにそれらを接着する接着樹脂層の厚さが薄く
なり、シール性、イージーピール性、層間接着強度等の
本来必要な性能が付与できなくなるため好ましくない。
成形性を考慮すると50〜90%の範囲とすることがよ
り好ましく、さらには非晶性ポリエステル樹脂層の厚さ
をポリブチレンテレフタレート樹脂層の厚さの5倍以上
に設定することが好ましい。
The polyester resin used for the amorphous polyester resin layer adjacent to the PBT layer is not limited to homotype and copolymer type resins, but the moldability is required and the crystallinity must be suppressed as low as possible. Particularly in the case of a homotype resin having a high crystallinity, it is necessary to rapidly cool the film after forming it into an amorphous state. Further, "PETG" manufactured by Eastman Chemical Co., which is a copolyester resin using terephthalic acid as an acid component and ethylene glycol and 1,4-cyclohexanedimethanol as an alcohol component, is amorphous and can be preferably used. Here, the thickness of the amorphous polyester resin layer is required to be 30 to 90% of the whole, because this is to cover the moldability of the outer layer PBT having poor moldability, and if it is less than 30%, There is a very high possibility that the property will be insufficient and the waist will also be low, which is not preferable. On the contrary, if it exceeds 80%, the thickness of the seal layer, the easy peel layer and the adhesive resin layer for adhering them becomes thin, and the originally required performances such as sealing property, easy peel property and interlayer adhesive strength cannot be imparted, which is preferable. Absent.
Considering the moldability, it is more preferably in the range of 50 to 90%, and further, it is preferable to set the thickness of the amorphous polyester resin layer to 5 times or more the thickness of the polybutylene terephthalate resin layer.

【0007】シール層はMIが5〜30(JIS K
7210 試験温度:190℃、試験荷重:2.16k
gf(21.18N)の低密度ポリエチレンが好適に使
用できる。これは座薬包装機の機構上、成形の予熱時成
形部が若干融着する現象が見られ、その融着した部分が
成形されたとき成形の力でフィルムが層間剥離を起こす
ことを防止するため、ホットタック性の劣る高圧法で重
合された低密度ポリエチレンが融着した部分の剥離強度
が低く優れていることによるものである。さらにMIが
5〜30、より好ましくは10〜25の範囲であること
が、溶融時の流動性が高く、融着部が剥がれやすくなる
ため好適である。MIが5未満となると融着部の剥がれ
が悪くフィルムの層間剥離を起こす危険性がある。また
フィルムの破断強度が強くなり、凝集破壊層の破壊によ
る開封時にフィルムが破断し難くなり、膜残り現象を発
生させやすくなる。逆にMIが30を越えると製膜し難
くなるという問題がある。また厚さは1〜15μmさら
に好ましくは1〜10μmであることが望まれるが、1
5μmを越えるような場合は前述したようにフィルムの
破断強度が強くなり、凝集破壊層の破壊による開封時に
フィルムが破断し難く、膜残り現象を発生させ易くなる
ためである。
The seal layer has an MI of 5 to 30 (JIS K
7210 Test temperature: 190 ° C, test load: 2.16k
A low density polyethylene of gf (21.18N) can be preferably used. This is due to the mechanism of the suppository packaging machine, a phenomenon in which the molding part is slightly fused during preheating of the molding is observed, and when the fused part is molded, the force of molding prevents the film from delaminating. This is because the peel strength of the fused portion of the low-density polyethylene polymerized by the high-pressure method having poor hot tack property is low and excellent. Further, it is preferable that MI is in the range of 5 to 30, more preferably 10 to 25 because the fluidity at the time of melting is high and the fused portion is easily peeled off. When the MI is less than 5, peeling of the fusion-bonded portion is poor and there is a risk of delamination of the film. Further, the breaking strength of the film is increased, the film is less likely to be broken at the time of opening due to the breakage of the cohesive failure layer, and the film residual phenomenon is likely to occur. On the other hand, when the MI exceeds 30, it is difficult to form a film. The thickness is desired to be 1 to 15 μm, more preferably 1 to 10 μm.
This is because when the thickness exceeds 5 μm, the breaking strength of the film becomes strong as described above, the film is less likely to break at the time of opening due to the breakage of the cohesive failure layer, and the film residual phenomenon is likely to occur.

【0008】凝集破壊層に使用される樹脂は特に限定さ
れず、エチレン−酢酸ビニル共重合体(EVA)とポリ
プロピレン(PP)の混合体、直鎖低密度ポリエチレン
(LL)とポリブテン−1(PB−1)の混合体、アイ
オノマーとPPの混合体等、通常知られている樹脂の組
み合わせが可能である。ここで、凝集破壊層の厚さは1
〜15μm、さらに好ましくは1〜10μmである。こ
れは凝集破壊時の糸引きを抑えるため極力凝集破壊層の
厚さを薄くする必要があるためである。しかし1μm以
下ではイージーピール層が薄くなり過ぎ、イージーピー
ル強度の安定性に問題が発生する可能性が出てくる。ま
た15μmを越えると糸引きが多く発生し、剥離外観が
悪くなる問題が発生し易い。
The resin used in the cohesive failure layer is not particularly limited, and is a mixture of ethylene-vinyl acetate copolymer (EVA) and polypropylene (PP), linear low density polyethylene (LL) and polybutene-1 (PB). It is possible to use a combination of commonly known resins such as a mixture of -1) and a mixture of an ionomer and PP. Here, the thickness of the cohesive failure layer is 1
˜15 μm, more preferably 1 to 10 μm. This is because it is necessary to reduce the thickness of the cohesive failure layer as much as possible in order to suppress stringing during cohesive failure. However, if the thickness is 1 μm or less, the easy peel layer becomes too thin, which may cause a problem in stability of the easy peel strength. On the other hand, if it exceeds 15 μm, a large amount of stringing occurs, and the problem of deteriorating the peeled appearance tends to occur.

【0009】本発明フィルムの製膜方法は特に限定され
ないが、各層厚さを最適厚さに設定できる共押出方法が
最も好ましい。また座薬包装用フィルムの場合、非晶性
ポリエステル樹脂層に酸化チタン等を添加し白色等の着
色を施すことができる。座薬用フィルムは一般に同一の
フィルムを成形、シールし包装しているが、本発明のフ
ィルムも同様に使用することが可能である。但し両側に
イージーピールが施されている場合よりも、片側に完全
シールのタイプのフィルム(例:PBT/非晶性ポリエ
ステル樹脂/AD/LDPE)を使用することにより、
イージーピールが単一層で行われるため剥離が安定し、
より膜残り等の発生しない安定したイージーピール性を
得ることができる。
The film forming method of the film of the present invention is not particularly limited, but a coextrusion method capable of setting the thickness of each layer to an optimum thickness is most preferable. Further, in the case of a suppository packaging film, titanium oxide or the like can be added to the amorphous polyester resin layer to give a coloring such as white. The suppository film is generally formed by molding, sealing and packaging the same film, but the film of the present invention can be used in the same manner. However, by using a completely seal type film (eg PBT / amorphous polyester resin / AD / LDPE) on one side rather than the case where easy peel is applied on both sides,
Easy peeling is performed in a single layer, so peeling is stable,
It is possible to obtain a stable easy peeling property in which no film residue is generated.

【0010】また酸素バリアー性の付与のため、層構成
中にエチレン−酢酸ビニル共重合体けん化物等の酸素バ
リアー層を配することもできる。
In order to impart an oxygen barrier property, an oxygen barrier layer such as saponified ethylene-vinyl acetate copolymer may be arranged in the layer structure.

【0011】[0011]

【実施例】以下、本発明の実施例を示すが、本発明はこ
れに限定されるものではない。実施例1〜2及び比較例
1〜6のフィルムを共押出法及び/又は押出ラミネート
法にて製膜し、評価を行った。
EXAMPLES Examples of the present invention will be shown below, but the present invention is not limited thereto. The films of Examples 1 and 2 and Comparative Examples 1 to 6 were formed by a coextrusion method and / or an extrusion laminating method and evaluated.

【0012】(実施例1) [層構成] PBT/PETG/AD/ LL+PP/LDPE (5μm/105μm/10μm/ 5μm/ 5μm) PBT:ノバデュール5010(三菱エンジニアリング
プラスチックス(株)社製) PETG:イースターPETG6763(イーストマン
ケミカル(株)社製) AD:アドマーSF731(三井化学(株)社製) LL+PP: LL:ノバテックLL UF240(日本ポリケム
(株)社製) PP:ノバテックPP FW3E(日本ポリケム(株)
社製) LDPE:ノバテックLD LC720(日本ポリケム
(株)社製) 上記組成の原料樹脂を用いてTダイ共押出法にて製膜し
た。
(Example 1) [Layer constitution] PBT / PETG / AD / LL + PP / LDPE (5 μm / 105 μm / 10 μm / 5 μm / 5 μm) PBT: Novadur 5010 (manufactured by Mitsubishi Engineering Plastics Co., Ltd.) PETG: Easter PETG6763 (manufactured by Eastman Chemical Co., Ltd.) AD: Admer SF731 (manufactured by Mitsui Chemicals, Inc.) LL + PP: LL: Novatec LL UF240 (manufactured by Nippon Polychem Co., Ltd.) PP: Novatec PP FW3E (Japan Polychem Co., Ltd.) )
LDPE: Novatec LD LC720 (manufactured by Nippon Polychem Co., Ltd.) A raw material resin having the above composition was used to form a film by a T-die coextrusion method.

【0013】(実施例2) [層構成] PBT/PETG/AD/EVOH/AD/EVA+P
P/LDPE (5μm/84μm/7μm/15μm/7μm/7μ
m/ 5μm) EVOH:ソアノールAT4403(日本合成化学
(株)社製) EVA+PP: EVA:ノバテックEVA LV350(日本ポリケム
(株)社製) PP:ノバテックPP FW3E(日本ポリケム(株)
社製) 他は実施例1と同じ原料。上記組成の原料樹脂を用いて
Tダイ共押出法にて製膜した。
(Example 2) [Layer structure] PBT / PETG / AD / EVOH / AD / EVA + P
P / LDPE (5μm / 84μm / 7μm / 15μm / 7μm / 7μ
m / 5 μm) EVOH: Soarnol AT4403 (manufactured by Nippon Synthetic Chemical Industry Co., Ltd.) EVA + PP: EVA: Novatec EVA LV350 (manufactured by Nippon Polychem Co., Ltd.) PP: Novatec PP FW3E (Nippon Polychem Co., Ltd.)
Other products are the same as in Example 1. A film was formed by the T-die coextrusion method using the raw material resin having the above composition.

【0014】(比較例1) [層構成] PETG/ AD /LL+PP/LDPE ( 110μm/10μm/ 5μm/ 5μm) 実施例1と同一原料を用いてTダイ共押出法にて製膜し
た。
Comparative Example 1 [Layer Structure] PETG / AD / LL + PP / LDPE (110 μm / 10 μm / 5 μm / 5 μm) The same raw material as in Example 1 was used to form a film by the T-die coextrusion method.

【0015】(比較例2) [層構成] PBT/ AD /LL+PB−1/LDPE (110μm/10μm/ 5μm/ 5μm) 実施例1と同一原料を用いてTダイ共押出法にて製膜し
た。
Comparative Example 2 [Layer Structure] PBT / AD / LL + PB-1 / LDPE (110 μm / 10 μm / 5 μm / 5 μm) The same raw material as in Example 1 was used to form a film by the T-die coextrusion method.

【0016】(比較例3) [層構成] PBT/PETG//LDPE (5μm/95μm//30μm) 実施例1と同一原料を用いてPBT/PETGからなる
共押出シートを製膜し、ついでLDPEを押出ラミネー
トした。PETGとLDPEの層間で剥離して開封す
る。
Comparative Example 3 [Layer Constitution] PBT / PETG // LDPE (5 μm / 95 μm // 30 μm) A coextruded sheet of PBT / PETG was formed using the same raw material as in Example 1, and then LDPE was formed. Was extrusion laminated. The PETG and LDPE layers are separated and opened.

【0017】(比較例4) [層構成] PBT/PETG/ AD/LL+PP/LDPE ( 30μm/80μm/10μm/5μm/ 5μm
) 実施例1と同一原料を用いてTダイ共押出法にて製膜し
た。
(Comparative Example 4) [Layer Structure] PBT / PETG / AD / LL + PP / LDPE (30 μm / 80 μm / 10 μm / 5 μm / 5 μm
) The same raw material as in Example 1 was used to form a film by the T-die coextrusion method.

【0018】(比較例5) [層構成] PBT/ PETG/ AD /LDPE/LL+PP
/LDPE ( 20μm/35μm/10μm/45μm/ 10
μm/10μm ) 実施例1と同一原料を用いてTダイ共押出法にて製膜し
た。
(Comparative Example 5) [Layer constitution] PBT / PETG / AD / LDPE / LL + PP
/ LDPE (20 μm / 35 μm / 10 μm / 45 μm / 10
μm / 10 μm) The same raw material as in Example 1 was used to form a film by T-die coextrusion method.

【0019】(比較例6) [層構成] PBT/PETG/AD/LL+PP/LDPE ( 2μm/120μm/3μm/ 2μm/ 2μm) 実施例1と同一原料を用いてTダイ共押出法にて製膜し
た。
Comparative Example 6 [Layer Structure] PBT / PETG / AD / LL + PP / LDPE (2 μm / 120 μm / 3 μm / 2 μm / 2 μm) The same raw material as in Example 1 was used to form a film by T-die coextrusion method. did.

【0020】<評価方法>上記各フィルムを用い、通常
の座薬包装機により座薬の包装を行い、性能を評価し
た。(フィルムは、両側ともに同一のフィルムを使用し
た)
<Evaluation Method> Using each of the above films, suppositories were packaged by an ordinary suppository packaging machine, and the performance was evaluated. (The film used the same film on both sides)

【0021】・成形性:型どおりの成形が可能か否かを
評価し、型どおりの成形ができたものを○とした。 ・シール性:シール時、熱板取られ現象が発生しないか
どうかを評価し、熱板取られがないものを○とした。 ・イージーピール性:開封時の剥離状態を観察し、膜残
り、糸引き等の問題がなく、きれいに剥離可能なものを
○とした。 評価結果を表1に示した。
Moldability: Whether or not molding according to the mold was possible was evaluated, and those that could be molded according to the mold were evaluated as ◯. -Sealability: When the hot plate was peeled off during sealing, it was evaluated whether or not the phenomenon occurred. -Easy peeling property: The peeling state at the time of opening was observed, and there were no problems such as film residue and stringing, and those that could be peeled off neatly were rated as ◯. The evaluation results are shown in Table 1.

【0022】[0022]

【表1】 [Table 1]

【0023】表1より本発明の複合フィルムを使用した
実施例1、2はいずれの性能にも優れていることが分か
る。これに対して、比較例1乃至6についてはいずれか
の性能に劣り座薬包装用として不都合がなことが分か
る。
It can be seen from Table 1 that Examples 1 and 2 using the composite film of the present invention are excellent in both performances. On the other hand, it is understood that Comparative Examples 1 to 6 are inferior to any of the performances and are inconvenient for suppository packaging.

【0024】[0024]

【発明の効果】本発明によれば、成形性、シール性、及
びイージーピール性が良好で、座薬包装用に好適に使用
できる複合フィルムが得られる。
EFFECTS OF THE INVENTION According to the present invention, a composite film having good moldability, sealing property and easy peeling property, which can be suitably used for suppository packaging, can be obtained.

フロントページの続き Fターム(参考) 3E086 AB01 BA04 BA15 BA24 BB51 BB90 CA28 4F100 AK06C AK07D AK41B AK42A AK68D AL05D AR00D BA04 BA07 BA10A BA10C GB15 GB66 JA12B JA20A JA20B JK01D JL01 JL12C JL14 YY00A YY00B YY00C Continued front page    F term (reference) 3E086 AB01 BA04 BA15 BA24 BB51                       BB90 CA28                 4F100 AK06C AK07D AK41B AK42A                       AK68D AL05D AR00D BA04                       BA07 BA10A BA10C GB15                       GB66 JA12B JA20A JA20B                       JK01D JL01 JL12C JL14                       YY00A YY00B YY00C

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 少なくとも外層よりポリブチレンテレフ
タレート樹脂層、非晶性ポリエステル樹脂層、凝集破壊
層、シール層の順に積層され、ポリブチレンテレフタレ
ート樹脂層の厚さが全体の1〜20%、非晶性ポリエス
テル樹脂層の厚さが全体の30〜90%であることを特
徴とする複合フィルム。
1. A polybutylene terephthalate resin layer, an amorphous polyester resin layer, a cohesive failure layer, and a seal layer are laminated in this order from at least the outer layer, and the thickness of the polybutylene terephthalate resin layer is 1 to 20% of the whole, and the amorphous The composite film, wherein the thickness of the conductive polyester resin layer is 30 to 90% of the whole.
【請求項2】 シール層がメルトインデックス(MI)
5〜30の低密度ポリエチレン樹脂であることを特徴と
する請求項1記載の複合フィルム。
2. The seal layer has a melt index (MI).
It is a low-density polyethylene resin of 5-30, The composite film of Claim 1 characterized by the above-mentioned.
【請求項3】 凝集破壊層の厚さが1〜15μm、シー
ル層の厚さが1〜15μmであることを特徴とする請求
項1又は2記載の複合フィルム。
3. The composite film according to claim 1, wherein the cohesive failure layer has a thickness of 1 to 15 μm and the sealing layer has a thickness of 1 to 15 μm.
【請求項4】 座薬包装用であることを特徴とする請求
項1乃至3のいずれか1項記載の複合フィルム。
4. The composite film according to claim 1, which is used for packaging suppositories.
JP2001366051A 2001-11-30 2001-11-30 Composite film Expired - Fee Related JP3904906B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001366051A JP3904906B2 (en) 2001-11-30 2001-11-30 Composite film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001366051A JP3904906B2 (en) 2001-11-30 2001-11-30 Composite film

Publications (2)

Publication Number Publication Date
JP2003165189A true JP2003165189A (en) 2003-06-10
JP3904906B2 JP3904906B2 (en) 2007-04-11

Family

ID=19176005

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001366051A Expired - Fee Related JP3904906B2 (en) 2001-11-30 2001-11-30 Composite film

Country Status (1)

Country Link
JP (1) JP3904906B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2018012201A (en) * 2016-07-19 2018-01-25 三菱ケミカル株式会社 Coextrusion multilayer film for deep-drawn package, and bottom material for deep-drawn package and deep-drawn package using the same
JP2018030255A (en) * 2016-08-22 2018-03-01 三菱ケミカル株式会社 Non-stretched coextrusion film for lid material and package

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2018012201A (en) * 2016-07-19 2018-01-25 三菱ケミカル株式会社 Coextrusion multilayer film for deep-drawn package, and bottom material for deep-drawn package and deep-drawn package using the same
JP2018030255A (en) * 2016-08-22 2018-03-01 三菱ケミカル株式会社 Non-stretched coextrusion film for lid material and package

Also Published As

Publication number Publication date
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