JP3218066B2 - Heat shrinkable foam composite sheet - Google Patents

Heat shrinkable foam composite sheet

Info

Publication number
JP3218066B2
JP3218066B2 JP2088892A JP2088892A JP3218066B2 JP 3218066 B2 JP3218066 B2 JP 3218066B2 JP 2088892 A JP2088892 A JP 2088892A JP 2088892 A JP2088892 A JP 2088892A JP 3218066 B2 JP3218066 B2 JP 3218066B2
Authority
JP
Japan
Prior art keywords
heat
acid
shrinkable
sheet
composite sheet
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.)
Expired - Lifetime
Application number
JP2088892A
Other languages
Japanese (ja)
Other versions
JPH06240037A (en
Inventor
木 和 彦 鈴
辺 孝 行 渡
原 泰 広 北
岡 正 伸 味
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.)
Mitsui Chemicals Inc
Original Assignee
Mitsui Chemicals 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 Mitsui Chemicals Inc filed Critical Mitsui Chemicals Inc
Priority to JP2088892A priority Critical patent/JP3218066B2/en
Publication of JPH06240037A publication Critical patent/JPH06240037A/en
Application granted granted Critical
Publication of JP3218066B2 publication Critical patent/JP3218066B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Laminated Bodies (AREA)
  • Biological Depolymerization Polymers (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明は熱収縮性発泡複合シート
に関する。さらに詳しくは、乳酸ポリマーを主体とする
熱可塑性ポリマー組成物からなる、自然環境下での分解
性を持った熱収縮性複合発泡シートに関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat-shrinkable foamed composite sheet. More specifically, the present invention relates to a heat-shrinkable composite foamed sheet made of a thermoplastic polymer composition mainly composed of a lactic acid polymer and having degradability in a natural environment.

【0002】[0002]

【従来の技術】従来、ワンウェイ用ガラス壜のラベルと
して使用されている熱収縮性発泡複合シートは、発泡ポ
リスチレン系樹脂や発泡ポリプロピレン系樹脂が主流を
なしている。しかしこのような樹脂から製造された熱収
縮性発泡複合シートは、廃棄する際、ゴミの量を増すう
えに、従来の物は自然環境下での分解速度がきわめて遅
いため、埋設処理された場合、半永久的に地中に残留す
る。また投棄されたプラスチック類により、景観が損な
われ海洋生物の生活環境が破壊されるなどの問題もあ
る。然しながら、これまで、自然環境下で容易に分解し
てしまう熱収縮性発泡複合シートは知られていない。
2. Description of the Related Art Conventionally, as a heat-shrinkable foamed composite sheet used as a label for a one-way glass bottle, a foamed polystyrene resin or a foamed polypropylene resin is mainly used. However, heat-shrinkable foamed composite sheets made from such a resin increase the amount of garbage when discarded.In addition, conventional products have a very low decomposition rate in the natural environment. , Remains in the ground semi-permanently. There is also a problem that the dumped plastics damage the landscape and destroy the living environment of marine life. However, a heat-shrinkable foamed composite sheet that is easily decomposed in a natural environment has not been known.

【0003】一方、熱可塑性で生分解性のあるポリマー
として、ポリ乳酸または乳酸とヒドロキシカルボン酸
コポリマーが知られている。この乳酸ポリマーは、動物
の体内で数ケ月から1年の内に100%生分解する。ま
た、土壌や海水中に放置された場合、湿った環境下では
数週間で分解を始め、約1年で消滅する。分解生成物
は、乳酸と二酸化炭素と水であり、すべて無害である。
On the other hand, polylactic acid or a copolymer of lactic acid and hydroxycarboxylic acid is known as a thermoplastic and biodegradable polymer. This lactic acid polymer is 100% biodegradable in the body of an animal within a few months to a year. When left in soil or seawater, it starts to decompose in a few weeks in a humid environment and disappears in about one year. The decomposition products are lactic acid, carbon dioxide and water, all harmless.

【0004】原料となる乳酸は、コーンスターチやコー
ンシロップのような安価な材料の発酵から得られ、ま
た、エチレンのような石油化学原料からも得られる。ポ
リ乳酸または乳酸のコポリマーの製造に関しては、米
国特許 1,995,970に開示されており、通常ラクタイドと
呼ばれる乳酸の環状2量体から合成されている。この乳
酸系ポリマーは、その生体適合と分解性から手術用の縫
合糸や、医学用の徐放性材料として用いられているが、
熱収縮性発泡複合シートとして用いることはいまだ知ら
れていない。
[0004] The raw material lactic acid is obtained from fermentation of inexpensive materials such as corn starch and corn syrup, and also from petrochemical raw materials such as ethylene. The preparation of polylactic acid or copolymers with lactic acid is disclosed in U.S. Pat. No. 1,995,970, which is synthesized from a cyclic dimer of lactic acid commonly called lactide. This lactic acid-based polymer is used as a surgical suture or a sustained-release material for medicine because of its biocompatibility and degradability.
Use as a heat-shrinkable foamed composite sheet has not yet been known.

【0005】[0005]

【発明が解決しようとする課題】本発明は、自然環境下
で分解可能な熱収縮性を有する発泡ポリ乳酸系シートと
ポリ乳酸系フィルムを貼り合わせた複合シートを提供す
ることにある。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a composite sheet in which a foamed polylactic acid-based sheet and a polylactic acid-based film, which are decomposable in a natural environment and have heat shrinkability, are bonded to each other.

【0006】[0006]

【課題を解決するための手段】本発明者らは、自然環境
下で分解可能な熱収縮性発泡複合シートを得る目的で、
乳酸系ポリマに着目し、乳酸ポリマーを主体とする樹
脂からなる熱収縮性発泡シートと該樹脂からなるフィル
ムを貼り合わせた複合シートを得、更にポリマーの持っ
ている分解性を損なうことなく熱収縮性発泡複合シート
が得られることを見い出し本発明を完成した。即ち、本
発明は、ポリ乳酸または乳酸とヒドロキシカルボン酸の
コポリマーよりなる熱可塑性ポリマー組成物からなる熱
収縮性発泡シートと該熱可塑性ポリマー組成物からなる
フィルムより構成されていることを特徴とする熱収縮性
発泡複合シートである。
Means for Solving the Problems The inventors of the present invention aimed at obtaining a heat-shrinkable foamed composite sheet which can be decomposed in a natural environment.
Heat without paying attention to lactic acid-based polymer over, lactate polymer obtained the bonded composite sheet film comprising a heat-shrinkable foamed sheet and the resin made of a resin mainly composed of, impairing degradability have further the polymer It has been found that a shrinkable foamed composite sheet can be obtained, and the present invention has been completed. That is, the present invention is characterized in that it is constituted by a film made of a heat-shrinkable foamed sheet and a thermoplastic polymer composition comprising a thermoplastic polymer composition comprising a copolymer of polylactic acid or lactic acid and hydroxycarboxylic acid It is a heat-shrinkable foamed composite sheet.

【0007】本発明に用いられるポリマーは、ポリ乳酸
と他のヒドロキシカルボン酸のポリマーとの混合物、ま
たは乳酸と他のヒドロキシカルボン酸とのコポリマーで
ある。他のヒドロキシカルボン酸としては、グリコール
酸、3−ヒドロキシ酪酸、4−ヒドロキシ酪酸、4−ヒ
ドロキシ吉草酸、5−ヒドロキシ吉草酸、6−ヒドロキ
シカプロン酸等が用いられる。
[0007] The polymer used in the present invention is a mixture of polylactic acid and a polymer of another hydroxycarboxylic acid, or a copolymer of lactic acid and another hydroxycarboxylic acid. As other hydroxycarboxylic acids, glycolic acid, 3-hydroxybutyric acid, 4-hydroxybutyric acid, 4-hydroxyvaleric acid, 5-hydroxyvaleric acid, 6-hydroxycaproic acid and the like are used.

【0008】これらのポリマーは、乳酸、あるいは他の
ヒドロキシカルボン酸から直接脱水重縮合することによ
って合成したものでも良いし、ラクタイド、またはグリ
コライドやε−カプロラクトン、またはそれらの混合物
を開環重合することによって得られた物でも良い。また
ポリ乳酸と他のヒドロキシカルボン酸のポリマーを高温
下エステル交換反応することによって合成したコポリマ
ーでも良い。ポリマーを構成する乳酸は、L−乳酸また
はD−乳酸またはそれらの混合物のいずれでもよい。
[0008] These polymers may be those synthesized by direct dehydration polycondensation from lactic acid or other hydroxycarboxylic acids, or ring-opening polymerization of lactide, or glycolide or ε-caprolactone, or a mixture thereof. A product obtained by doing so may be used. Alternatively, a copolymer synthesized by subjecting a polymer of polylactic acid and another hydroxycarboxylic acid to a transesterification reaction at a high temperature may be used. The lactic acid constituting the polymer may be L-lactic acid, D-lactic acid or a mixture thereof.

【0009】ポリマーの平均分子量は、1万から100
万が好ましい。これより低い分子量ではフィルム等の成
形品にしたときの強度が小さく実用に適さない。また、
これより分子量が高いと、熱的溶融した状態での粘度が
高く成形加工性が劣る。また本発明のポリマー組成物は
可塑剤、改質剤等を含んでいてもよい。
The average molecular weight of the polymer is between 10,000 and 100
10,000 is preferred. If the molecular weight is lower than this, the strength of a molded article such as a film is small and is not suitable for practical use. Also,
If the molecular weight is higher than this, the viscosity in a thermally molten state is high and the moldability is poor. Further, the polymer composition of the present invention may contain a plasticizer, a modifier and the like.

【0010】本発明でいう熱収縮性発砲シートは、厚み
が0.1〜1.0mm、好ましくは、0.15〜0.5
mmであって、160℃に加熱した際、シートの巻き上
げ方向に大きく収縮するものであって、好ましくは、一
方方向に30%以上収縮し、また、それと直角方向が1
0%未満の収縮する性質を有するものである。一方方向
に30%未満の収縮では、ポリ乳酸系のフィルムを貼り
合わせた複合シートを矩形に裁断し、端面をシールして
円筒状体を作成した後、容器に装着して加熱した際、容
器に密着しない。また、容器に密着した円筒状体で高さ
方向が10%を越えた収縮性能を有していると、収縮後
の装着位置がズレて商品価値を損なう。熱収縮性発泡シ
ートは、任意の方法を用いて実施することができる。通
常は、発泡剤を用いた押出機から押し出すと同時に発泡
させるいわゆる押出発泡を用いることが好ましい。
The heat-shrinkable foam sheet according to the present invention has a thickness of
Is 0.1 to 1.0 mm, preferably 0.15 to 0.5
mm, when heated to 160 ° C., shrinks greatly in the winding direction of the sheet, and preferably shrinks by 30% or more in one direction, and the direction perpendicular to the direction is 1% or more.
It has the property of shrinking less than 0%. When the shrinkage is less than 30% in one direction, the composite sheet laminated with the polylactic acid-based film is cut into a rectangular shape, and the end surface is sealed to form a cylindrical body. Does not adhere to In addition, if the cylindrical body in close contact with the container has a shrinkage performance in which the height direction exceeds 10%, the mounting position after shrinkage is shifted and the commercial value is impaired. The heat-shrinkable foam sheet can be implemented using any method. Usually, it is preferable to use what is called extrusion foaming, in which foaming is performed simultaneously with extrusion from an extruder using a foaming agent.

【0011】発泡剤としては、蒸発により発泡させる蒸
発型発泡剤、例えばブタン、ペタン、プロパン等の炭化
水素や、塩化メチル、モノクロルトリフルオロメタン、
ジクロルジフルオロメタン、ジクロルテトラフルオロエ
タン等のハロゲン化合物や炭酸ガス、窒素ガスがあげら
れる。これらの発泡剤の添加量は、ポリマー組成物に対
して0.1〜30重量%、特に0.5〜10重量%が好
ましい。
Examples of the foaming agent include evaporative foaming agents that foam by evaporation, for example, hydrocarbons such as butane, petane and propane, methyl chloride, monochlorotrifluoromethane,
Examples thereof include halogen compounds such as dichlorodifluoromethane and dichlorotetrafluoroethane, carbon dioxide gas, and nitrogen gas. The addition amount of these blowing agents is preferably 0.1 to 30% by weight, particularly preferably 0.5 to 10% by weight , based on the polymer composition.

【0012】また必要に応じて、加熱すると分解してガ
スを発生する分解型発泡剤、例えば重炭酸ソーダ等の無
機発泡剤、アゾジカルボンアミド、N,N’−ジニトロ
ソペンタメチレンテトラミン、p,p’オキシビス(ベ
ンゼンスルホニルヒドラジド)等の有機発泡剤や発泡助
剤あるいは核剤、例えばステアリン酸、シュウ酸、サリ
チル酸、フタル酸、安息香酸、クエン酸、酒石酸等の無
機酸、前記有機酸または無機酸の塩、炭酸ソーダ等の炭
酸塩、酸化亜鉛、酸化カルシュウム、酸化チタン、シリ
カ、クレイ等を適当量加えてもよい。
If necessary, a decomposition-type blowing agent that decomposes to generate a gas upon heating, for example, an inorganic blowing agent such as sodium bicarbonate, azodicarbonamide, N, N'-dinitrosopentamethylenetetramine, p, p ' Organic blowing agents such as oxybis (benzenesulfonyl hydrazide), foaming aids or nucleating agents such as stearic acid, oxalic acid, salicylic acid, phthalic acid, benzoic acid, citric acid, tartaric acid, etc .; Salts, carbonates such as sodium carbonate, zinc oxide, calcium oxide, titanium oxide, silica, clay and the like may be added in appropriate amounts.

【0013】熱収縮性発泡シートの押出温度は、ポリマ
ーの組成によって異なるが、通常溶融粘度が10,00
0〜100,000ポイズになる温度で行う。これより
低いと溶融したポリマーの粘度が高く気泡の生成が遅く
発泡倍率が上がらない。逆にこれより高い温度でポリマ
ーの粘度が小さすぎると気泡を保持できなくなり、均一
な品質の発泡シートが得られない。発泡倍率は1.5〜
10倍が好ましい。
The extrusion temperature of the heat-shrinkable foam sheet varies depending on the composition of the polymer.
Performed at a temperature of 0-100,000 poise. If it is lower than this, the viscosity of the molten polymer is high and the generation of bubbles is slow, and the expansion ratio does not increase. Conversely, if the viscosity of the polymer is too low at a temperature higher than this, bubbles cannot be retained, and a uniform quality foam sheet cannot be obtained. Foaming ratio is 1.5 ~
10 times is preferred.

【0014】熱収縮性発泡シートの収縮性能は、前記原
料を押出機にて加熱混合した後、大気中に放出してシー
トを引取る工程で付与する。
The shrinkage performance of the heat-shrinkable foamed sheet is imparted in a step of heating and mixing the raw materials in an extruder and then releasing the raw materials into the atmosphere to take out the sheet.

【0015】ポリ乳酸系フィルムは、厚みが0.01〜
0.05mm、好ましくは0.015〜0.03mmで
あり、発泡剤と核剤等を使用せずポリ乳酸系ポリマー
で、フィルムとしたものを、一方方向に延伸したもので
ある。尚、ポリ乳酸系フィルムは熱収縮性発泡シート
類似の熱収縮性能を有するものが好ましい。
The polylactic acid-based film has a thickness of 0.01 to
It is 0.05 mm, preferably 0.015 to 0.03 mm, and is obtained by stretching a film made of a polylactic acid-based polymer without using a foaming agent and a nucleating agent in one direction. Incidentally, the polylactic acid-based film preferably has a heat shrinkage performance similar to that of the heat shrinkable foam sheet .

【0016】また、熱収縮性発泡シートにおいて、片面
にポリ乳酸系の樹脂で0.005〜0.05mmの非発
泡層を有する2層構造の共押出発泡シートは接着面に該
非発泡層を配置することとなり、ポリ乳酸系フィルムと
の平滑性を維持し、ポリ乳酸系フィルムとの接着力を増
大させる為好適である。一方、印刷は熱収縮性発泡シー
あるいはポリ乳酸系フィルムの裏側に施し、熱収縮性
発泡シートとポリ乳酸系フィルムで挟まれる様にする。
好ましくはポリ乳酸系フィルムに印刷を施す。
In the heat-shrinkable foamed sheet , a two-layer coextruded foamed sheet having a non-foamed layer of 0.005 to 0.05 mm of a polylactic acid resin on one side is provided with the non-foamed layer disposed on an adhesive surface. This is suitable for maintaining the smoothness with the polylactic acid-based film and increasing the adhesive strength with the polylactic acid-based film. On the other hand, printing is performed on heat-shrinkable foam
Applied to the back side of the bets or polylactic acid film, heat-shrinkable
It is sandwiched between a foam sheet and a polylactic acid-based film.
Preferably, printing is performed on the polylactic acid-based film.

【0017】熱収縮性発泡シートとポリ乳酸系フィルム
の貼り合わせは、通常の方法を用いて実施することが出
来る。即ち、フィルムを加熱して熱収縮性発泡シート
直接溶着したり、接着性の熱可塑性樹脂をバインダーと
して使用して、所望のものが得られる。
The lamination of the heat-shrinkable foam sheet and the polylactic acid-based film can be carried out by a usual method. That is, a desired product can be obtained by heating the film and directly welding it to the heat-shrinkable foamed sheet , or by using an adhesive thermoplastic resin as a binder.

【0018】[0018]

【実施例】以下、実施例により本発明を詳細に説明す
る。 実施例1〜3熱収縮性発泡シート 表−1に示す分子量約10万のポリD、L−ラクタイド
とポリL−ラクタイド混合物100重量部にタルク(ミ
クロエース;日本タルク製)0.5重量部とフロン22
(三井デュポンフロロケミカル製)5重量部を発砲層の
原料とし、一方、分子量約10万のポリD、L−ラクタ
イドとポリL−ラクタイド混合物100重量部を非発砲
層の原料として共押出方法にて得た二層構造の熱収縮性
発泡シートであって、該発泡シートは厚さが発泡層で
0.20mm、非発砲層で0.019mmであり、16
0℃に加熱した際の収縮率が押出方向に50%、それと
直角方向に4%であるシート。
The present invention will be described below in detail with reference to examples. Examples 1 to 3 Heat-shrinkable foam sheet 0.5 parts by weight of talc (Microace; manufactured by Nippon Talc) was added to 100 parts by weight of a mixture of poly D, L-lactide and poly L-lactide having a molecular weight of about 100,000 shown in Table 1. And Freon 22
5 parts by weight (manufactured by Mitsui DuPont Fluorochemicals) was used as a raw material for the foaming layer, while 100 parts by weight of a mixture of poly D, L-lactide and poly L-lactide having a molecular weight of about 100,000 was used as a raw material for the non-foaming layer. The heat-shrinkable foamed sheet having a two-layer structure obtained as described above, wherein the foamed sheet has a thickness of 0.20 mm in the foamed layer, 0.019 mm in the non-foamed layer, and a thickness of 16 mm.
A sheet having a shrinkage ratio of 50% in the extrusion direction when heated to 0 ° C. and 4% in a direction perpendicular thereto.

【0019】ポリ乳酸系フィルム 表−1に示す分子量約10万のポリD、L−ラクタイド
とポリL−ラクタイド混合物100重量部をインフレー
ション成形で成膜したもので、160℃の加熱時、押出
方向の収縮率が35%であり、それと直角方向の収縮率
が8%である、厚み0.020mmのフィルム。ポリ乳
酸系フィルムには、フィルムを通して文字、図柄が読め
る様に印刷を施した。
Polylactic acid-based film A film formed by inflation molding of 100 parts by weight of a mixture of poly D, L-lactide and poly L-lactide having a molecular weight of about 100,000 shown in Table 1. The film having a thickness of 0.020 mm having a shrinkage of 35% and a shrinkage of 8% in a direction perpendicular thereto. The polylactic acid-based film was printed so that characters and designs could be read through the film.

【0020】前記の熱収縮性発泡シートとポリ乳酸系フ
ィルムの貼り合わせは190℃の熱ロールでフィルムを
加熱して、発泡シートに直接接着した。ポリ乳酸系フィ
ルムの表面性を損なうことなく平滑で光沢があった。ま
たこの複合シートを100mm巾のリング状にスリット
して、ガラス壜に巻き付けるべくラッピング機で試験し
た。ラベルは安定して裁断され、寸法精度も高くロスが
少なかった。ラベルの巻き付いたガラス壜を200℃の
シュリンクトンネル中を通過させると、壜の肩および低
部に密着するまで収縮した。
The above-mentioned heat-shrinkable foam sheet and the polylactic acid-based film were bonded together by heating the film with a hot roll at 190 ° C. to directly adhere to the foam sheet. The polylactic acid film was smooth and glossy without impairing the surface properties. This composite sheet was slit into a ring having a width of 100 mm and tested by a wrapping machine so as to be wound around a glass bottle. The label was cut stably, with high dimensional accuracy and low loss. When the glass bottle with the label was passed through a 200 ° C. shrink tunnel, it shrunk until it adhered to the shoulder and lower part of the bottle.

【0021】被覆壜を温度35℃、水分30%の土壌中
に埋設して複合シートの分解試験を行った。分解性の評
価は、外観変化と重量の減少率で判定した。結果を表−
1に併記した。 比較例1熱収縮性発泡シート の収縮率が一方方向に25%、それ
と直角方向に3%の性能を有する以外は実施例1と同様
にして複合シートを得た。得られた複合シートを壜に巻
き付け、シュリンクトンネル中を通しても充分収縮せず
収縮ムラが発生した。
The composite sheet was subjected to a decomposition test by burying the coated bottle in soil at a temperature of 35 ° C. and a water content of 30%. Degradability was evaluated based on the change in appearance and the rate of weight loss. Table-Results
Also described in 1. Comparative Example 1 A composite sheet was obtained in the same manner as in Example 1 except that the heat-shrinkable foamed sheet had a performance of 25% in one direction and 3% in a direction perpendicular thereto. The obtained composite sheet was wound around a bottle and did not shrink sufficiently even through a shrink tunnel, resulting in uneven shrinkage.

【0022】[0022]

【表1】 実施例4〜6 表−2に示すL−ラクタイドとオキシカルボン酸のコポ
リマーを用いる他は実施例1と同様にして、熱収縮性発
砲複合シートを製造した。結果は同じく表−2に示す。
[Table 1] Examples 4 to 6 Heat-shrinkable foamed composite sheets were produced in the same manner as in Example 1 except that copolymers of L-lactide and oxycarboxylic acid shown in Table 2 were used. The results are also shown in Table 2.

【0023】[0023]

【表2】 [Table 2]

【0024】[0024]

【発明の効果】本発明によるポリ乳酸または乳酸とヒド
ロキシカルボン酸のコポリマーよりなる熱可塑性ポリマ
ー組成物からなる熱収縮性発泡複合シートは緩衝性、耐
熱性に優れ、更に光沢がよく美しい外観を持った壜被覆
用ラベルを得ることができ、また廃棄物として地中に埋
設されたり海や川に投棄された場合、紙や木等の天然物
と同じように自然環境中で比較的短い期間の内に無害な
水と炭酸ガスに分解する。
The heat-shrinkable foamed composite sheet comprising a thermoplastic polymer composition comprising polylactic acid or a copolymer of lactic acid and hydroxycarboxylic acid according to the present invention has excellent buffering properties and heat resistance, and has good gloss and beautiful appearance. Bottle cover labels and, when buried underground as waste or dumped into the sea or rivers, can be used for a relatively short period of time in the natural environment, similar to natural products such as paper and wood. Decomposes into harmless water and carbon dioxide.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B32B 5/18 B32B 27/36 C08J 9/04 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 7 , DB name) B32B 5/18 B32B 27/36 C08J 9/04

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】ポリ乳酸または乳酸とヒドロキシカルボン
酸のコポリマーよりなる熱可塑性ポリマー組成物からな
る熱収縮性発泡シートと該熱可塑性ポリマー組成物から
なるフィルムより構成されていることを特徴とする熱収
縮性発泡複合シート。
1. A heat-shrinkable foamed sheet comprising a thermoplastic polymer composition comprising polylactic acid or a copolymer of lactic acid and hydroxycarboxylic acid, and a film comprising the thermoplastic polymer composition. Shrinkable foam composite sheet.
【請求項2】乳酸がL−乳酸、D−乳酸またはそれらの
混合物であることを特徴とする請求項1記載の熱収縮性
発泡複合シート。
Wherein lactic acid is L- lactate, D- lactic acid or heat-shrinkable foamed composite sheet of claim 1, wherein the mixtures thereof.
【請求項3】ヒドロキシカルボン酸がグリコール酸であ
ることを特徴とする請求項1記載の熱収縮性発泡複合シ
ート。
3. The heat-shrinkable foamed composite sheet according to claim 1, wherein the hydroxycarboxylic acid is glycolic acid.
【請求項4】熱収縮性ポリ乳酸系発泡シートの熱収縮性
能が160℃に加熱した際、一方方向に30%以上収縮
し、それと直角方向が10%未満の収縮する性質を有す
るものであることを特徴とする請求項1項載の熱収縮性
発泡複合シート。
4. The heat-shrinkable polylactic acid-based foamed sheet has a heat-shrinking property in that when heated to 160 ° C., it shrinks by 30% or more in one direction and shrinks by less than 10% in a direction perpendicular thereto.
Heat-shrinkable foamed composite sheet of the mounting according to claim 1, wherein, characterized in that the shall.
JP2088892A 1992-02-06 1992-02-06 Heat shrinkable foam composite sheet Expired - Lifetime JP3218066B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2088892A JP3218066B2 (en) 1992-02-06 1992-02-06 Heat shrinkable foam composite sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2088892A JP3218066B2 (en) 1992-02-06 1992-02-06 Heat shrinkable foam composite sheet

Publications (2)

Publication Number Publication Date
JPH06240037A JPH06240037A (en) 1994-08-30
JP3218066B2 true JP3218066B2 (en) 2001-10-15

Family

ID=12039754

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2088892A Expired - Lifetime JP3218066B2 (en) 1992-02-06 1992-02-06 Heat shrinkable foam composite sheet

Country Status (1)

Country Link
JP (1) JP3218066B2 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3330712B2 (en) * 1994-01-11 2002-09-30 三菱樹脂株式会社 Method for producing polylactic acid-based film
JPH07205278A (en) * 1994-01-11 1995-08-08 Mitsubishi Plastics Ind Ltd Production of stretched film of polylactic acid polymer
JP3328418B2 (en) * 1994-03-28 2002-09-24 三菱樹脂株式会社 Heat-shrinkable polylactic acid film
JP3330273B2 (en) * 1996-01-11 2002-09-30 三菱樹脂株式会社 Heat-shrinkable polylactic acid-based film and method for producing the same
JP4731044B2 (en) * 2001-05-22 2011-07-20 独立行政法人理化学研究所 Stretched film and cell culture substrate using the same
JP2003002984A (en) * 2002-06-14 2003-01-08 Mitsubishi Plastics Ind Ltd Polylactic acid film
JP4583160B2 (en) * 2004-12-20 2010-11-17 日本ポリプロ株式会社 Biodegradable laminated foam sheet and molded body thereof
CN104401078B (en) * 2014-12-17 2017-03-22 南通大学 Multilayer polylactic acid composite plate and preparation method thereof

Also Published As

Publication number Publication date
JPH06240037A (en) 1994-08-30

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