JP2006198931A - Biodegradable laminated film and sealed bag - Google Patents

Biodegradable laminated film and sealed bag Download PDF

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Publication number
JP2006198931A
JP2006198931A JP2005013982A JP2005013982A JP2006198931A JP 2006198931 A JP2006198931 A JP 2006198931A JP 2005013982 A JP2005013982 A JP 2005013982A JP 2005013982 A JP2005013982 A JP 2005013982A JP 2006198931 A JP2006198931 A JP 2006198931A
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laminated film
bag
film
sealed bag
lactic acid
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Takashi Moriya
貴史 森谷
Takashi Sumiki
隆 隅木
Shoichi Yoshida
章一 吉田
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DIC Corp
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Dainippon Ink and Chemicals Co Ltd
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Priority to JP2005013982A priority Critical patent/JP2006198931A/en
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W90/00Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
    • Y02W90/10Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics

Abstract

<P>PROBLEM TO BE SOLVED: To provide a biodegradable laminated film which not only indicates flexibility and impact resistance but also has an appearance excellent in transparency and glossiness, increases the commercial value of an article to be packaged, is capable of a good bag making aptitude by a bag making machine especially when used as a melt-cut sealed bag film for packaging, and prevents the breakage of the bag when contents is put in the obtained sealed bag and the sealed bag obtained by using the laminated film. <P>SOLUTION: The biodegradable laminated film comprises a layer containing poly(butylene succinate adipate) between layers containing polylactic acid. The sealed bag is obtained by melt-cutting/sealing the laminated film. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、透明で包装用フィルムとして好適な柔軟性と耐衝撃性を有する生分解性積層フィルムとこの積層フィルムから得られるシール袋に関するものである。   The present invention relates to a biodegradable laminated film that is transparent and suitable as a packaging film and has impact resistance and a sealing bag obtained from the laminated film.

一般に包装用フィルムは、内容物がよく見えるように透明性を有するポリプロピレンやポリエチレンテレフタレートのフィルムが用いられ、商品の陳列効果を高めるべく、より光沢のある透明フィルムが求められている。しかしながら、上記ポリプロピレンやポリエチレンテレフタレートといった樹脂は、使用後焼却処分あるいは埋め立て処分するしかなく、近年の環境保護の観点からは環境負荷の少ない材料への転換が求められている。   In general, a packaging film is made of a transparent polypropylene or polyethylene terephthalate film so that the contents can be seen well, and a transparent film with higher gloss is required to enhance the display effect of the product. However, the above-mentioned resins such as polypropylene and polyethylene terephthalate can only be disposed of by incineration or landfill after use, and from the viewpoint of environmental protection in recent years, conversion to a material with less environmental load is required.

環境に配慮する観点から、土中あるいは水中で加水分解や生分解によって最終的には二酸化炭素と水に分解される生分解性樹脂が注目されている。
かかる生分解性樹脂において、ポリ乳酸に代表されるガラス転移点が室温以上の硬質タイプは、透明性は良好であり、前記包装用フィルムの要求に応えるものであるが、非常に硬くて脆い材料であり、包装用フィルムとしての性能を満足するものではない。
From the viewpoint of consideration for the environment, biodegradable resins that are finally decomposed into carbon dioxide and water by hydrolysis or biodegradation in soil or water are drawing attention.
In such a biodegradable resin, a hard type having a glass transition point represented by polylactic acid having a glass transition temperature of room temperature or higher has good transparency and meets the requirements of the packaging film, but is a very hard and brittle material. Therefore, the performance as a packaging film is not satisfied.

このポリ乳酸の脆い性質を改善するために、可塑剤等を配合して軟質化するなどの技術が知られている(例えば特許文献1参照。)。また、ポリ乳酸系重合体にガラス転移点が0℃以下の生分解性脂肪族ポリエステルを配合して耐衝撃性を向上させる技術が知られている(例えば特許文献2参照。)。
しかしながら、可塑剤を配合したフィルムは、滑り性が悪化するため、製袋機等への適応性が低下したり、長期保管によって可塑剤のブリードによって透明性が悪化し、実用的でない。また、ガラス転移点が0℃以下の脂肪族ポリエステルを配合した場合は、透明性が損なわれ、前記方法用フィルムとしての要求を満足するものではない。
In order to improve the brittle nature of this polylactic acid, a technique of softening by blending a plasticizer or the like is known (for example, see Patent Document 1). In addition, a technique for improving impact resistance by blending a polylactic acid polymer with a biodegradable aliphatic polyester having a glass transition point of 0 ° C. or less is known (see, for example, Patent Document 2).
However, since a film blended with a plasticizer deteriorates in slipperiness, the adaptability to a bag making machine or the like decreases, or transparency deteriorates due to bleeding of the plasticizer due to long-term storage, which is not practical. Further, when an aliphatic polyester having a glass transition point of 0 ° C. or lower is blended, transparency is impaired, and the requirements for the method film are not satisfied.

一方、ポリブチレンサクシネートやポリブチレンアジペート−テレフタレート共重合体に代表されるガラス転移点が0℃以下の脂肪族ポリエステルおよび脂肪族−芳香族ポリエステル等比較的軟質の生分解性樹脂は、柔軟性はあるが白濁するため透明性に欠けるものであり、包装用フィルムとして適用するには美粧性に欠けるものであった。   On the other hand, relatively soft biodegradable resins such as aliphatic polyesters and aliphatic-aromatic polyesters having a glass transition point of 0 ° C. or lower, such as polybutylene succinate and polybutylene adipate-terephthalate copolymer, are flexible. However, since it becomes cloudy, it lacks transparency, and lacks cosmetics when applied as a packaging film.

特開平7−177826号公報(第1−7頁)JP-A-7-177826 (pages 1-7) 特開平9−111107号公報(第1−6頁)JP-A-9-111107 (page 1-6)

本発明は、柔軟性と耐衝撃性を有し、透明性と高い光沢を備えた包装用フィルムとして好適な生分解性を有する積層フィルムとこの積層フィルムを用いてなるシール袋を提供することにある。   The present invention is to provide a laminated film having flexibility and impact resistance, suitable as a packaging film having transparency and high gloss, and having a biodegradability, and a sealing bag using the laminated film. is there.

本発明者等は、上記課題を解決すべく鋭意検討を重ねた結果、乳酸系重合体からなる層間に、特定の脂肪族ポリエステルからなる中間樹脂層を共押出法によって積層させたフィルムが透明性および光沢が良好で、柔軟性と耐衝撃性を有し、且つ、ツイストバッグ製袋機で容易に製袋でき、十分な実用性を備えたシール袋をもたらすことを見出し、本発明を完成するに至った。
すなわち、本発明は、乳酸系重合体を含有する層間にポリ(ブチレンサクシネート−アジペート)を含有してなる層を有する生分解性積層フィルムを提供し、且つこの積層フィルムを溶断シールしてなるシール袋を提供するものである。
As a result of intensive studies to solve the above problems, the present inventors have found that a film in which an intermediate resin layer made of a specific aliphatic polyester is laminated between layers made of a lactic acid polymer by a coextrusion method is transparent. The present invention is completed by finding a sealing bag that has good gloss, flexibility, impact resistance, can be easily made with a twist bag making machine, and has sufficient practicality. It came to.
That is, the present invention provides a biodegradable laminated film having a layer containing poly (butylene succinate-adipate) between layers containing a lactic acid polymer, and the laminated film is fused and sealed. A seal bag is provided.

本発明の積層フィルムは、柔軟性や耐衝撃性の特性を示すばかりでなく、透明、光沢、に優れた外観を有し、包装物品の商品価値を高め、特に包装用溶断シール袋フィルムとして用いた場合、製袋機で良好な製袋適性が可能で、得られるシール袋に内容物を入れる際も袋が破れることないものである。   The laminated film of the present invention not only exhibits flexibility and impact resistance, but also has an excellent appearance in terms of transparency and gloss, enhances the commercial value of packaging articles, and is particularly used as a fusing seal bag film for packaging. If it is, the bag making machine can have good bag making suitability, and the bag is not torn when the contents are put into the obtained seal bag.

本発明の積層フィルムにおいて、乳酸系重合体を含有する樹脂層は表面層及び裏面層を構成し、それぞれ単層構成または多層構成の樹脂層である。かかる表面層及び裏面層は、通常は同じものであるが、本発明の目的を達成すれば異なっていてもよい。また、表面層及び裏面層がそれぞれ多層である場合も、本発明の目的を達成する限りに於いて成分的に相違していてもよい。
前記乳酸系重合体としては、特に限定されないが、ポリ(D−乳酸)と、ポリ(L−乳酸)と、D−乳酸とL−乳酸との共重合体と、D−乳酸と他のヒドロキシカルボン酸との共重合体あるいはL−乳酸と他のヒドロキシカルボン酸との共重合体、あるいはこれらのブレンド物、また、ジカルボン酸およびジオールをエステル反応させて得られたポリエステル成分を乳酸成分と共重合させたものがあげられ、なかでも、主たる構造単位がL−乳酸であるポリ乳酸が成膜安定性の点から特に好ましい。
また、乳酸系重合体を含有する樹脂層としては、本発明の目的を損なわない範囲で上記乳酸系重合体の他にジカルボン酸およびジオールをエステル反応させて得られるポリエステル成分を混合して用いることができる。この際のかかるポリエステル成分の含有量としては、好ましくは該樹脂層中で30重量%以下である。
In the laminated film of the present invention, the resin layer containing a lactic acid polymer constitutes a surface layer and a back surface layer, and is a resin layer having a single layer structure or a multilayer structure, respectively. Such front and back layers are usually the same, but may be different as long as the object of the present invention is achieved. Further, even when the front surface layer and the back surface layer are each multi-layered, they may be different from each other as long as the object of the present invention is achieved.
The lactic acid-based polymer is not particularly limited, but poly (D-lactic acid), poly (L-lactic acid), a copolymer of D-lactic acid and L-lactic acid, D-lactic acid and other hydroxys. A copolymer with a carboxylic acid or a copolymer of L-lactic acid with another hydroxycarboxylic acid, or a blend thereof, or a polyester component obtained by ester reaction of a dicarboxylic acid and a diol with a lactic acid component. Polymerized ones are mentioned, and polylactic acid whose main structural unit is L-lactic acid is particularly preferable from the viewpoint of film formation stability.
In addition, as a resin layer containing a lactic acid polymer, a polyester component obtained by subjecting a dicarboxylic acid and a diol to an ester reaction in addition to the above lactic acid polymer is used within a range not impairing the object of the present invention. Can do. The content of the polyester component at this time is preferably 30% by weight or less in the resin layer.

上記ヒドロキシカルボン酸、ジオールおよびジカルボン酸としては、グリコール酸、ヒドロキシ酪酸、ヒドロキシカプロン酸等のヒドロキシカプロン酸類、カプロラクトン、ブチロラクトン、ラクチド、グリコリド等の環状ラクトン類などのヒドロキシカルボン酸;エチレングリコール、プロピレングリコール、1,4−ブタンジオール、1,4−シクロヘキサンジメタノールなどの脂肪族ジオール;テレフタル酸、イソフタル酸、ナフタレンジカルボン酸などの芳香族ジカルボン酸;コハク酸、アジピン酸、スベリン酸、セバシン酸などの脂肪族ジカルボン酸である。   Examples of the hydroxycarboxylic acid, diol, and dicarboxylic acid include hydroxycaproic acids such as glycolic acid, hydroxybutyric acid, and hydroxycaproic acid, and hydroxycarboxylic acids such as cyclic lactones such as caprolactone, butyrolactone, lactide, and glycolide; ethylene glycol, propylene glycol Aliphatic diols such as 1,4-butanediol and 1,4-cyclohexanedimethanol; aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid and naphthalenedicarboxylic acid; succinic acid, adipic acid, suberic acid and sebacic acid It is an aliphatic dicarboxylic acid.

乳酸系重合体を含有する樹脂層としては、押出成形時に良好な流動性を有する必要からメルトフローレートが190℃において好ましくは0.5〜20g/10min、より好ましくは2〜10g/10minである。かかるメルトフローレートの範囲であると、押出成形が容易であり、また、共押出多層化するときに、隣接層との流動性も良好でより外観に優れた積層フィルムが得られる。   As a resin layer containing a lactic acid-based polymer, the melt flow rate is preferably 0.5 to 20 g / 10 min at 190 ° C., more preferably 2 to 10 g / 10 min, because it needs to have good fluidity during extrusion molding. . When the melt flow rate is within this range, extrusion molding is easy, and when co-extrusion multilayering is performed, a laminated film having good flowability with an adjacent layer and more excellent appearance can be obtained.

本発明の積層フィルムにおいて、ポリブチレンサクシネート−アジペート共重合体を含有する樹脂層は、上記乳酸系重合体を含有する樹脂層の間に積層され、単層構成または多層構成の樹脂層である。ポリブチレンサクシネート−アジペート共重合体を含有する樹脂層が多層である場合、本発明の目的を達成する限りに於いてそれぞれ成分的に相違していてもよい。また、該樹脂層には、実質的に乳酸系重合体を含有しないが、本発明の目的を損なわない範囲、すなわち樹脂層中に乳酸系重合体を30重量%以下で含有することができる。
なお、ポリブチレンサクシネート−アジペート共重合体を含有する樹脂層のメルトフローレート(190℃)は、0.5〜20g/10min程度がフィルム押出成形性の点から好ましく、さらに好ましくは1〜10g/10minである。
In the laminated film of the present invention, the resin layer containing the polybutylene succinate-adipate copolymer is laminated between the resin layers containing the lactic acid-based polymer, and is a resin layer having a single layer configuration or a multilayer configuration. . When the resin layer containing the polybutylene succinate-adipate copolymer is a multilayer, it may be different from each other as long as the object of the present invention is achieved. In addition, the resin layer does not substantially contain a lactic acid polymer, but the resin layer can contain a lactic acid polymer in an amount that does not impair the object of the present invention, that is, 30% by weight or less.
The melt flow rate (190 ° C.) of the resin layer containing the polybutylene succinate-adipate copolymer is preferably about 0.5 to 20 g / 10 min from the point of film extrusion moldability, more preferably 1 to 10 g. / 10 min.

上記ポリブチレンサクシネート−アジペート共重合体としては、例えば、ポリブチレンサクシネートにアジピン酸を共重合して結晶化度を低下させたものであるが、ポリブチレンサクシネート、ポリブチレンアジペート/テレフタレート共重合体、ポリカプロラクトン等のポリエステルを本発明の目的を損なわない範囲で混合して用いても構わない。かかるポリブチレンサクシネート−アジペート共重合体の樹脂層中の含有量は、少なくとも30重量%である。   As the polybutylene succinate-adipate copolymer, for example, polybutylene succinate is copolymerized with adipic acid to reduce the crystallinity, but polybutylene succinate, polybutylene adipate / terephthalate copolymer Polymers and polyesters such as polycaprolactone may be mixed and used as long as the object of the present invention is not impaired. The content of the polybutylene succinate-adipate copolymer in the resin layer is at least 30% by weight.

本発明の積層フィルムの厚さ(全厚)と、乳酸系重合体を含有する樹脂層による表面層および裏面層並びにポリブチレンサクシネート−アジペート共重合体を含有する樹脂層の厚さについては、用途等によって異なり、特に限定されるものではないが、全厚は包装用フィルムとして好適に使用できることから、通常15〜150μmであり、なかでも20〜100μmが好ましい。かかる表面層および裏面層の厚さは、それぞれ2〜20μmであることが好ましく、なかでも透明性を保持するためにも、5μm以上であることがより好ましい。また、ポリブチレンサクシネート−アジペート共重合体を含有する樹脂の厚さは、10μm以上であることが必須であり、なかでも10〜90μmであることが耐衝撃性の点から好ましい。
尚、本発明の積層フィルムは、靱性を損なわないように適度な透明性を有しているものが好ましく、JIS K7105による曇り度が好ましくは20%以下、より好ましくは8〜12%である
About the thickness (total thickness) of the laminated film of the present invention, and the thickness of the resin layer containing the front and back layers and the polybutylene succinate-adipate copolymer by the resin layer containing the lactic acid-based polymer, Although it changes with uses etc. and it is not specifically limited, Since the total thickness can be used conveniently as a film for packaging, it is 15-150 micrometers normally, and 20-100 micrometers is especially preferable. The thickness of each of the surface layer and the back layer is preferably 2 to 20 μm, and more preferably 5 μm or more in order to maintain transparency. Further, the thickness of the resin containing the polybutylene succinate-adipate copolymer is essential to be 10 μm or more, and in particular, 10 to 90 μm is preferable from the viewpoint of impact resistance.
The laminated film of the present invention preferably has moderate transparency so as not to impair toughness, and the haze according to JIS K7105 is preferably 20% or less, more preferably 8 to 12%.

本発明の積層フィルムには、上記各樹脂層のいずれかあるいは全ての層に他の熱可塑性樹脂、造核剤、熱安定剤、帯電防止剤、アンチブロッキング剤、スリップ剤、防曇剤等を本発明の目的を損なわない範囲で添加しても良い。   In the laminated film of the present invention, other thermoplastic resins, nucleating agents, thermal stabilizers, antistatic agents, antiblocking agents, slip agents, antifogging agents, etc. are added to any or all of the above resin layers. You may add in the range which does not impair the objective of this invention.

本発明の積層フィルムの製造方法としては、上記各樹脂層が隣接して積層される共押出積層成形法であることが必要であり、例えば、2台以上の押出機を用いて溶融押出する、共押出多層ダイス法、フィードブロック法等の公知の共押出法により溶融状態で各樹脂層を積層した後、インフレーション、Tダイ・チルロール法等の方法で長尺巻フィルムに加工する方法が好ましく、Tダイを用いた共押出法がより好ましい。   As a production method of the laminated film of the present invention, it is necessary to be a coextrusion lamination molding method in which the resin layers are laminated adjacent to each other, for example, melt extrusion using two or more extruders, After laminating each resin layer in a molten state by a known coextrusion method such as a coextrusion multilayer die method, a feed block method, etc., a method of processing into a long wound film by a method such as inflation, T-die chill roll method, A coextrusion method using a T die is more preferred.

本発明の共押出積層フィルムの製造に際して最外樹脂層には、印刷の接着性や接着剤との接着性を向上させるために、表面処理を施してもよい。
この表面処理の方法は、本発明の共押出積層フィルムを連続的に処理でき、かつ、製膜時に巻き取る前に容易に実施でき、処理の度合いも任意に調整できるコロナ放電処理が望ましい。なお、表面処理に関しては加熱下または不活性ガスの雰囲気下でコロナ放電もしくはプラズマ放電等の効果促進手法を用いても良い。
In the production of the coextruded laminated film of the present invention, the outermost resin layer may be subjected to a surface treatment in order to improve the adhesiveness for printing and the adhesiveness with the adhesive.
The surface treatment method is preferably a corona discharge treatment that can continuously treat the coextruded laminated film of the present invention, can be easily carried out before winding during film formation, and can arbitrarily adjust the degree of treatment. As for the surface treatment, an effect promoting method such as corona discharge or plasma discharge may be used under heating or in an inert gas atmosphere.

而して、得られる本発明の積層フィルムを製袋機、好ましくはツイストバッグ製袋機を用いて溶断製袋することにより、シール袋を製造することができる。この際、積層フィルムを2つ折りに重ねて、好ましくは加熱温度280〜320℃でシール部分を加熱して接着し、溶断することにより連続的に行われる。勿論、適宜切り出した2枚の積層フィルムを重ねてシール部分を加熱することによりシール袋を製造することもできる。   Thus, a sealed bag can be produced by fusing and making the resulting laminated film of the present invention using a bag making machine, preferably a twist bag making machine. In this case, the laminated film is continuously folded in two, preferably by heating and adhering the sealing portion at a heating temperature of 280 to 320 ° C., and fusing. Of course, a sealing bag can be produced by stacking two laminated films appropriately cut out and heating the sealing portion.

本発明の積層フィルムは、柔軟性や耐衝撃性の特性を有し、透明、光沢に優れた外観を有するため、包装物品、特に包装用シール袋に好適に使用できる。   Since the laminated film of the present invention has flexibility and impact resistance characteristics, and has an appearance that is excellent in transparency and gloss, it can be suitably used for packaging articles, particularly packaging sealing bags.

以下に実施例と比較例を挙げて、本発明を具体的に説明するが、本発明はこれらに限定されるものではない。尚、例中の部及び%は全て重量基準である。   EXAMPLES The present invention will be specifically described below with reference to examples and comparative examples, but the present invention is not limited to these. In the examples, all parts and% are based on weight.

実施例1
乳酸系重合体を含有する樹脂層による表面層(a)および裏面層(c)としてL−乳酸を主体とする〔三井化学(株)製レイシアH−100:メルトフローレート8g/10min〕を用い、ポリブチレンサクシネート−アジペート共重合体を含有する樹脂層(b)としてポリブチレンサクシネート−アジペート共重合体〔昭和高分子製ビオノーレ#3001:メルトフローレート1.4g/10min〕用い、表面層(a)用押出機(口径30mm)と樹脂層(b)用押出機(口径40mm)と裏面層(c)用押出機(口径30mm)のそれぞれに樹脂を供給し、共押出法により押出温度230℃でTダイから(a)/(b)/(c)の各層の厚さが3μm/24μm/3μmになるように押出し、30℃の水冷金属冷却ロールで冷却し、ロールに巻き取り、35℃の熟成室で48時間熟成させて、全厚が30μmの本発明の共押出積層フィルムを得た。
Example 1
As the surface layer (a) and the back surface layer (c) by the resin layer containing a lactic acid-based polymer, L-lactic acid as a main component [Laisia H-100 manufactured by Mitsui Chemicals, Inc .: melt flow rate 8 g / 10 min] was used. The polybutylene succinate-adipate copolymer-containing resin layer (b) is a polybutylene succinate-adipate copolymer [Showon Polymer Bionore # 3001: Melt Flow Rate 1.4 g / 10 min], surface layer Resin is supplied to each of the extruder for (a) (diameter 30 mm), the extruder for resin layer (b) (diameter 40 mm), and the extruder for back layer (c) (diameter 30 mm), and the extrusion temperature is obtained by coextrusion method. Extrude at 230 ° C. from the T die so that the thickness of each layer (a) / (b) / (c) is 3 μm / 24 μm / 3 μm, cool with a 30 ° C. water-cooled metal cooling roll, Wound into Le, aged in maturing room 35 ° C. 48 h, total thickness was obtained coextruded laminated film of 30μm in the present invention.

実施例2
(a)/(b)/(c)の各層の厚さが4.5μm/21μm/4.5μmになるように押出した以外は実施例1と同様にして実施例2の共押出積層フィルムを得た。
Example 2
The coextruded laminated film of Example 2 was prepared in the same manner as in Example 1 except that each layer of (a) / (b) / (c) was extruded to have a thickness of 4.5 μm / 21 μm / 4.5 μm. Obtained.

比較例1
樹脂層(b)としてL−乳酸を主体とするポリ乳酸〔三井化学(株)製レイシアH−100〕を用いた以外は実施例1と同様にして比較例1の共押出積層フィルムを得た。
Comparative Example 1
A coextruded laminated film of Comparative Example 1 was obtained in the same manner as in Example 1 except that polylactic acid mainly composed of L-lactic acid [Lacia H-100 manufactured by Mitsui Chemicals, Inc.] was used as the resin layer (b). .

比較例2
表面層(a)、樹脂層(b)および裏面層(c)として、全てポリブチレンサクシネート−アジペート共重合体〔昭和高分子製ビオノーレ#3001〕用い用いた以外は実施例1と同様にして比較例2の共押出積層フィルムを得た。
Comparative Example 2
Example 1 except that polybutylene succinate-adipate copolymer [Bionole # 3001 manufactured by Showa Polymer Co., Ltd.] was used as the surface layer (a), resin layer (b) and back layer (c). A coextruded laminated film of Comparative Example 2 was obtained.

比較例3
表面層(a)、樹脂層(b)および裏面層(c)として、全てL−乳酸を主体とするポリ乳酸〔三井化学(株)製レイシアH−100〕とポリブチレンサクシネート−アジペート共重合体〔昭和高分子製ビオノーレ#3001〕を60/40の重量比率で混合して用いた以外は実施例1と同様にして比較例3の共押出積層フィルムを得た。
Comparative Example 3
As the surface layer (a), resin layer (b), and back layer (c), polylactic acid mainly composed of L-lactic acid [Lacia H-100 manufactured by Mitsui Chemicals, Inc.] and polybutylene succinate-adipate A coextruded laminated film of Comparative Example 3 was obtained in the same manner as in Example 1 except that the blend [Bionole # 3001 manufactured by Showa Polymer Co., Ltd.] was used by mixing at a weight ratio of 60/40.

得られた共押出多層フィルムの曇り度、剛性、0℃における衝撃強度および成膜性を下記の方法で評価および測定した。
(1)曇り度:JIS K7105
(2)剛性:ASTM−D882による25℃における1%接線モジュラスを測定した。
(3)衝撃強度:0℃に温度調節された恒温室で6時間状態調整したフィルムをその場でフィルムインパクト法によって測定した。
(4)成膜性:成膜中にフィルム切れやフィルム巻き付きなどが起こったものを×とし、成膜性が良好であったものを○とした。
The haze, rigidity, impact strength at 0 ° C. and film formability of the obtained coextruded multilayer film were evaluated and measured by the following methods.
(1) Cloudiness: JIS K7105
(2) Rigidity: 1% tangent modulus at 25 ° C. was measured according to ASTM-D882.
(3) Impact strength: A film conditioned for 6 hours in a temperature-controlled room adjusted to 0 ° C. was measured on the spot by the film impact method.
(4) Film formability: A film breakage or film wrapping occurred during film formation was marked with x, and a film with good film formability was marked with ◯.

得られた共押出多層フィルムの製袋性および溶断シール強度は、フィルムをトタニ技研工業(株)製ツイストバッグ製袋機HK−40Vを用いて、(c)層側を内側にして半折し、溶断刃300℃、製袋速度130枚/分で製袋し、溶断シール袋を得た。溶断シール部を15mm幅に切り出し、引張速度300mm/minで溶断シール強度を測定した。これらの結果を第1表に示す。   The coextrusion multilayer film obtained was made into a bag-forming property and fusing seal strength by using a twist bag bag making machine HK-40V manufactured by Totani Giken Kogyo Co., Ltd. The bag was made at a fusing blade of 300 ° C. and a bag-making speed of 130 sheets / min to obtain a fusing seal bag. The fusing seal part was cut out to a width of 15 mm, and the fusing seal strength was measured at a tensile speed of 300 mm / min. These results are shown in Table 1.

Figure 2006198931
Figure 2006198931

Claims (5)

乳酸系重合体を含有する層間にポリ(ブチレンサクシネート−アジペート)を含有してなる層を有する生分解性積層フィルム Biodegradable laminated film having a layer containing poly (butylene succinate-adipate) between layers containing a lactic acid polymer 前記乳酸系重合体のメルトフローレートが1〜20g/10minである請求項1記載の生分解性積層フィルム The biodegradable laminated film according to claim 1, wherein the lactic acid polymer has a melt flow rate of 1 to 20 g / 10 min. 前記ポリ(ブチレンサクシネート−アジペート)がメルトフローレート2〜10g/10minである請求項1又は2記載の生分解性積層フィルム。 The biodegradable laminated film according to claim 1 or 2, wherein the poly (butylene succinate-adipate) has a melt flow rate of 2 to 10 g / 10 min. JIS K7105による曇り度が20%以下である請求項1〜3のいずれかに記載の生分解性積層フィルム。 The biodegradable laminated film according to any one of claims 1 to 3, wherein the haze according to JIS K7105 is 20% or less. 請求項1〜4のいずれか1項記載の積層フィルムを溶断シールすることにより袋状に成形してなることを特徴とするシール袋。 A sealed bag formed by fusing and sealing the laminated film according to any one of claims 1 to 4 into a bag shape.
JP2005013982A 2005-01-21 2005-01-21 Biodegradable laminated film and sealed bag Pending JP2006198931A (en)

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