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JPH05140361A - Cushioning material - Google Patents

Cushioning material

Info

Publication number
JPH05140361A
JPH05140361A JP30058791A JP30058791A JPH05140361A JP H05140361 A JPH05140361 A JP H05140361A JP 30058791 A JP30058791 A JP 30058791A JP 30058791 A JP30058791 A JP 30058791A JP H05140361 A JPH05140361 A JP H05140361A
Authority
JP
Japan
Prior art keywords
acid
lactic acid
cushioning material
foam
lactide
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
JP30058791A
Other languages
Japanese (ja)
Other versions
JP3311371B2 (en
Inventor
Kazuhiko Suzuki
和彦 鈴木
Takayuki Watanabe
孝行 渡辺
Yasuhiro Kitahara
泰広 北原
Masanobu Ajioka
正伸 味岡
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 Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu 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 Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP30058791A priority Critical patent/JP3311371B2/en
Priority to CA002064410A priority patent/CA2064410A1/en
Priority to DE69214183T priority patent/DE69214183T2/en
Priority to EP92302840A priority patent/EP0507554B1/en
Publication of JPH05140361A publication Critical patent/JPH05140361A/en
Priority to US08/186,920 priority patent/US5447962A/en
Application granted granted Critical
Publication of JP3311371B2 publication Critical patent/JP3311371B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • C08J9/14Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
    • C08J9/143Halogen containing compounds
    • C08J9/147Halogen containing compounds containing carbon and halogen atoms only
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/04Polyesters derived from hydroxy carboxylic acids, e.g. lactones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

(57)【要約】 【目的】 ポリ乳酸または乳酸とヒドロシキカルボン酸
のコポリマーを主成分とする熱可塑性ポリマー組成物の
発泡体からなる緩衝材。 【効果】 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。
(57) [Abstract] [Purpose] A cushioning material made of a foam of a thermoplastic polymer composition containing polylactic acid or a copolymer of lactic acid and hydroxycarboxylic acid as a main component. [Effect] When it is buried in the ground as waste or dumped in the sea or river, it becomes harmless water and carbon dioxide gas in a relatively short period in the natural environment like natural products such as paper and trees. Disassemble.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は緩衝材に関する。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緩衝材
に関するものである。
FIELD OF THE INVENTION The present invention relates to a cushioning material. More specifically, the present invention relates to a cushioning material which is composed of a thermoplastic polymer composition mainly containing lactic acid polymer and has degradability in a natural environment.

【0002】[0002]

【従来の技術】従来、青果、生鮮食料品等傷つき易い物
の包装には、ポリスチレン系、ポリオレフィン系の発泡
シートをダンボール箱の角や中仕切りに使用したり、ネ
ット状になった発泡体を中仕切り板としたり、直接被せ
たりして広く用いている。特にこれらの発泡性の緩衝材
は、少量の樹脂で成形されており、目的を達成した後、
使い捨てられているのが現状である しかし、このような樹脂から成形した緩衝材は、廃棄す
る際、かさばり、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起こっている。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緩衝
材は知られていない。
2. Description of the Related Art Conventionally, polystyrene and polyolefin foam sheets have been used for the corners and partitions of cardboard boxes, and net foams have been used for the packaging of fragile items such as fruits and vegetables and fresh foods. Widely used as a partition plate or directly covered. In particular, these foamable cushioning materials are molded with a small amount of resin, and after achieving the purpose,
However, the cushioning material molded from such a resin is bulky and increases the amount of dust when discarded, and the conventional material has a very slow decomposition rate in the natural environment. Therefore, if buried, it will remain in the ground semipermanently. In addition, the discarded plastics have caused problems such as damage to the landscape and the living environment of marine life. However, hitherto, there is no known cushioning material that easily decomposes in a natural environment.

【0003】一方、分解性のある熱可塑性ポリマーとし
て、ポリ乳酸または乳酸のコポリマーが知られている。
この乳酸系ポリマーは、自然環境下で分解性があり、土
壌や海水中に置かれた場合、数週間で分解を始め、約一
年で消滅する。また分解生成物は乳酸と二酸価炭素と水
であり、すべて無害である。また原料となる乳酸は、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容
易に製造される。
On the other hand, polylactic acid or a copolymer of lactic acid is known as a degradable thermoplastic polymer.
This lactic acid-based polymer is degradable in a natural environment, and when placed in soil or seawater, it begins to decompose in a few weeks and disappears in about a year. The decomposition products are lactic acid, carbon dioxide and water, all of which are harmless. Lactic acid as a raw material is obtained from inexpensive fermentation such as corn starch and corn syrup, and is easily produced from petrochemical raw materials such as ethylene.

【0004】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、医学用の除放性材料とし
て用いられているが、緩衝材として用いることはいまだ
知られていない。
The preparation of polylactic acid or a copolymer of lactic acid is disclosed in US Pat. No. 1,995,970 and is synthesized from a cyclic dimer of lactic acid commonly referred to as lactide. Because of its biocompatibility and degradability, this lactic acid-based polymer is used as a surgical suture and a medical sustained-release material, but its use as a cushioning material 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
分解可能な緩衝材を提供することである。
SUMMARY OF THE INVENTION The present invention is to provide a cushioning material which can be decomposed in a natural environment.

【0006】[0006]

【課題を解決するための手段】本発明者らは、自然環境
下で分解可能な緩衝材を得る目的で、乳酸系ポリマーに
着目し、乳酸ポリマーを主体とする樹脂から発泡シート
またはネット状の発泡体を得、単独で使用するか、ある
いは紙等と貼り合わせて用いることにより、分解性を損
なうことなく緩衝性能を有するもの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を主成分と
する熱可塑性ポリマー組成物からなる緩衝材に関する。
The present inventors have focused their attention on lactic acid-based polymers for the purpose of obtaining a cushioning material that can be decomposed in a natural environment. It was found that a foam having a cushioning property can be obtained without impairing the decomposability by obtaining a foam and using it alone or laminating it with paper or the like, and completed the present invention. That is, the present invention relates to a buffer material composed of a thermoplastic polymer composition containing polylactic acid or a copolymer of lactic acid and hydroxycarboxylic acid as a main component.

【0007】本発明に用いられ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は、原料として乳酸
または乳酸の環状2量体であるラクタイド、さらにヒド
ロキシカルボン酸を用いるか、場合によってこの他のモ
ノマーを適宜使用できる。乳酸を用いる場合には脱水縮
合によるが、高分子量の物を得るにはラクタイドの開環
重合によるのが好ましい。開環重合に用いるラクタイド
は、L−ラクタイド、D−ラクタイド、mesoラクタ
イド、あるいはそれらの混合物が用いられるが、Dまた
はL−ラクタイドに、反対の光学活性が混ざった物が好
ましい。その混合割合は、DまたはL−ラクタイド/光
学対掌体=95/5〜50/50が好ましい。
The polylactic acid or the copolymer of lactic acid and hydroxycarboxylic acid used in the present invention uses lactic acid or lactide, which is a cyclic dimer of lactic acid, and hydroxycarboxylic acid as a raw material, or optionally other monomers as appropriate. Can be used. When lactic acid is used, dehydration condensation is used, but to obtain a high molecular weight product, ring-opening polymerization of lactide is preferable. As the lactide used in the ring-opening polymerization, L-lactide, D-lactide, meso lactide, or a mixture thereof is used, but a compound in which D and L-lactide have opposite optical activities is preferable. The mixing ratio is preferably D or L-lactide / optical antipode = 95/5 to 50/50.

【0008】乳酸系ポリマーの重合度は、150から2
0,000である。これより低い重合度ではフィルム等
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、重合度が高過ぎると、熱時溶融した状態での粘度が
高く、成形加工性が劣る。重合方法は、溶媒を用いる方
法でも、溶媒を用いない方法でも良いが、溶媒の回収の
問題から、工業的には溶媒を用いない塊状重合がよい。
開環重合の触媒は、一般に亜鉛、錫の塩化物またはカル
ボン酸塩等が用いられるが、特に限定されない。生体適
合性材料や食品関係に用いる場合は毒性を考慮する必要
がある。また、本発明による乳酸系ポリマーには可塑
剤、改質剤等を含んでいてもよい。
The degree of polymerization of the lactic acid type polymer is 150 to 2
It is 10,000. If the degree of polymerization is lower than this, the strength of a molded product such as a film is small and it is not suitable for practical use. On the other hand, if the degree of polymerization is too high, the viscosity in the molten state during heating is high and the moldability is poor. The polymerization method may be a method using a solvent or a method not using a solvent, but in view of the problem of solvent recovery, industrially bulk polymerization without a solvent is preferable.
As the ring-opening polymerization catalyst, zinc, tin chloride, carboxylate or the like is generally used, but the catalyst is not particularly limited. Toxicities should be considered when used in biocompatible materials and food products. The lactic acid-based polymer according to the present invention may contain a plasticizer, a modifier and the like.

【0009】本発明による緩衝材は乳酸系ポリマーを主
成分とする熱可塑性ポリマー組成物から製造されるが、
通常、上記熱可塑性ポリマーを用いて発泡シートまたは
発泡体を製造し、これを任意の形状にして緩衝材として
用いられる。発泡シートまたは発泡体の製造は通常の方
法を用いて実施することが出来る。即ち、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
発泡法を用いて製造でき、、発泡体の形状は押出機先端
に取り付けた金型を選択することで、所望のものが得ら
れる。発泡剤としては、蒸発により発泡させる蒸発発泡
剤、例えばエタン、ブタン、ペンタン、ヘキサン、ヘプ
タン、エチレン、プロピレン、石油エーテル等の炭化水
素、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
等のハロゲン化炭化水素や炭酸ガス、窒素ガス、水等が
挙げられる。これらの発泡剤の添加量は、熱可塑性ポリ
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。
The cushioning material according to the present invention is manufactured from a thermoplastic polymer composition containing a lactic acid-based polymer as a main component.
Usually, a foamed sheet or a foamed body is produced using the above-mentioned thermoplastic polymer, and this is formed into an arbitrary shape and used as a cushioning material. The production of the foamed sheet or foam can be carried out by using a usual method. That is, it can be produced by using a so-called extrusion foaming method in which foaming is simultaneously performed by extruding from an extruder using a foaming agent, and the shape of the foam can be obtained by selecting a mold attached to the tip of the extruder. Be done. Examples of the foaming agent include evaporative foaming agents that are foamed by evaporation, such as hydrocarbons such as ethane, butane, pentane, hexane, heptane, ethylene, propylene, petroleum ether, methyl chloride, monochlorotrifluoromethane, dichlorodifluoromethane, dichlorotetramethane. Examples thereof include halogenated hydrocarbons such as fluoroethane, carbon dioxide gas, nitrogen gas, and water. The amount of these foaming agents added is 0.1 to 30% by weight, particularly 0.5 to 30% by weight, based on the thermoplastic polymer composition.
10% by weight is preferred.

【0010】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
ペタメチレンテトラミン、p,p’−オキシビス(ベン
ゼンスルホニルカルバジド)、アゾビスイソブチロニト
リル、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、アルミナ、クレイ、カオリン、ケイソウ土
等を適当量加えてもよい。発泡成形品の着色その他の変
成のために、顔料、難燃剤、充填剤等を適当量加えるこ
とも何ら差し支えない。
If necessary, a decomposition-type foaming agent which decomposes to generate gas when heated, for example, an inorganic foaming agent such as sodium bicarbonate, azodicarbonamide, N, N'-dinitropetamethylenetetramine, p, p'- Organic foaming agents such as oxybis (benzenesulfonylcarbazide), azobisisobutyronitrile, benzenesulfonylhydrazide, foaming aids or nucleating agents such as stearic acid, oxalic acid, salicylic acid, phthalic acid, benzoic acid, citric acid, tartaric acid An appropriate amount of an inorganic acid such as the above, a salt of the organic acid or the inorganic acid, a carbonate such as sodium carbonate, zinc oxide, calcium oxide, titanium oxide, silica, alumina, clay, kaolin, diatomaceous earth and the like may be added. For coloring or other modification of the foamed molded product, it is also possible to add an appropriate amount of pigment, flame retardant, filler or the like.

【0011】発泡体の押出温度は、ポリマーの組成によ
って異なるが、通常溶融粘度が10,000〜100,
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。発泡倍率は緩衝材の性能によっ
て異なるが、5倍から25倍が好ましい。5倍未満の場
合、緩衝性能が不足し、被包装物を傷める。また、逆に
25倍を超えると発泡体の表面が脆くなる。発泡体の気
泡の大きさは0.1〜5mmΦが好ましい。0.1mm
Φ未満では、発泡体の製造時のロスが多い。また、5m
mΦを越えると表面が脆くなる。発泡体シートの場合、
シートを再加熱して軟化させた後、真空あるいは圧空成
形等の熱成形によって所望の形状に出来る。好ましく
は、部分的に穴を設けてシートの端面を多く有すること
が好ましい。発泡体がネット状のものは、所定の長さに
して被包装物に接触させて使用したり、紙と貼り合わせ
て中仕切り板や下敷き板として使用される。
The extrusion temperature of the foam varies depending on the composition of the polymer, but the melt viscosity is usually 10,000 to 100,
Perform at a temperature of 000 poise. If it is lower than this, the viscosity of the melted polymer is high, the formation of bubbles is slow, and the expansion ratio does not increase. On the other hand, if the viscosity of the polymer is too low at a temperature higher than this, bubbles cannot be retained, and a foamed sheet of uniform quality cannot be obtained. The expansion ratio depends on the performance of the cushioning material, but is preferably 5 to 25 times. If it is less than 5 times, the buffer performance is insufficient and the packaged item is damaged. On the other hand, when it exceeds 25 times, the surface of the foam becomes brittle. The bubble size of the foam is preferably 0.1 to 5 mmΦ. 0.1 mm
If it is less than Φ, there are many losses during the production of the foam. Also, 5m
If it exceeds mΦ, the surface becomes brittle. For foam sheets,
After the sheet is reheated to be softened, it can be formed into a desired shape by thermoforming such as vacuum or pressure forming. Preferably, it is preferable that the sheet has a large number of end faces by partially providing holes. The foam having a net shape is used by bringing it into a predetermined length so as to be brought into contact with an object to be packaged, or by being bonded to paper to be used as an intermediate partition plate or an underlay plate.

【0012】[0012]

【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 表−Iに示す分子量約10万のポリD,L−ラクタイド
とポリL−ラクタイド混合物に気泡調整剤としてタルク
0.5重量%を添加し、50mmΦの押出機で200℃
の温度で溶融混練した後、ブタンを樹脂100gに対し
0.065molの割合で圧入した。圧入後の押出機の
シリンダー温度を140〜175℃にして樹脂混合物を
冷却し、スリットより大気中に放出して厚みが2〜3m
m、650mm巾の発泡シートを得た。得られた発泡シ
ートの見掛け密度と緩衝性能(5/8の鋼球を46cm
の高さより落下させ、跳ね返る高さで判定;JIS K
−6382に準ずる)をそれぞれ表−Iに示した。この
発泡体を温度35℃、水分30%の土壌中に埋設して分
解試験を行った。分解性の評価は、重量の減少率で判定
した。結果を表−Iに併記した。
The present invention will be described in detail below with reference to examples. Examples 1 to 3 0.5% by weight of talc was added as a cell regulator to a mixture of poly D, L-lactide and poly L-lactide having a molecular weight of about 100,000 shown in Table-I, and the temperature was 200 ° C. in an extruder of 50 mmΦ.
After melt-kneading at the temperature of, butane was injected under pressure at a ratio of 0.065 mol to 100 g of the resin. After press fitting, the cylinder temperature of the extruder is set to 140 to 175 ° C. to cool the resin mixture, and the resin mixture is discharged into the atmosphere through the slit to have a thickness of 2 to 3 m.
A foamed sheet having a width of m and a width of 650 mm was obtained. Apparent density and cushioning performance of the obtained foamed sheet (46 cm for 5/8 steel balls)
Judgment from the height of the object and judgment by the height at which it bounces; JIS K
(Corresponding to -6382) are shown in Table-I. This foam was embedded in a soil having a temperature of 35 ° C. and a water content of 30% to perform a decomposition test. The degradability was evaluated by the weight reduction rate. The results are also shown in Table-I.

【0013】実施例4〜6 表−IIに示したL−ラクタイドとオキシカルボン酸のコ
ポリマーに変えた以外は実施例1と同様にして、発泡シ
ートを成形した。
Examples 4 to 6 Foam sheets were molded in the same manner as in Example 1 except that the copolymer of L-lactide and oxycarboxylic acid shown in Table II was used.

【0014】[0014]

【表1】 [Table 1]

【0015】[0015]

【表2】 [Table 2]

【0016】[0016]

【発明の効果】本発明の乳酸の主成分とするポリマーを
主体とする緩衝材は、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。
INDUSTRIAL APPLICABILITY The buffer material of the present invention, which is mainly composed of a polymer containing lactic acid as a main component, is the same as a natural product such as paper or wood when it is buried in the ground as waste or dumped in the sea or river. It decomposes into harmless water and carbon dioxide within a relatively short period of time in the natural environment.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 味岡 正伸 神奈川県横浜市栄区笠間町1190番地 三井 東圧化学株式会社内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Masanobu Amioka 1190 Kasama-cho, Sakae-ku, Yokohama-shi, Kanagawa Mitsui Toatsu Chemical Co., Ltd.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ポリ乳酸または乳酸とヒドロキシカルボ
ン酸のコポリマーを主成分とする熱可塑性ポリマー組成
物からなる緩衝材。
1. A buffer material comprising a thermoplastic polymer composition containing polylactic acid or a copolymer of lactic acid and hydroxycarboxylic acid as a main component.
【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記載の緩衝
材。
2. The cushioning material according to claim 1, wherein the lactic acid is L-lactic acid, D-lactic acid or a mixture 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記載の緩衝材。
3. The cushioning material according to claim 1, wherein the hydroxycarboxylic acid is glycolic acid.
JP30058791A 1991-04-01 1991-11-15 Cushioning material Expired - Lifetime JP3311371B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP30058791A JP3311371B2 (en) 1991-11-15 1991-11-15 Cushioning material
CA002064410A CA2064410A1 (en) 1991-04-01 1992-03-30 Degradable foam and use of same
DE69214183T DE69214183T2 (en) 1991-04-01 1992-03-31 Degradable foam, process for its production and its use
EP92302840A EP0507554B1 (en) 1991-04-01 1992-03-31 Degradable foam, process for its preparation and use of same
US08/186,920 US5447962A (en) 1991-04-01 1994-01-27 Degradable foam and use of same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30058791A JP3311371B2 (en) 1991-11-15 1991-11-15 Cushioning material

Related Child Applications (2)

Application Number Title Priority Date Filing Date
JP2002072467A Division JP2002275303A (en) 2002-03-15 2002-03-15 Foam
JP2002072466A Division JP2002363328A (en) 2002-03-15 2002-03-15 Foam sheet and foam sheet laminated body

Publications (2)

Publication Number Publication Date
JPH05140361A true JPH05140361A (en) 1993-06-08
JP3311371B2 JP3311371B2 (en) 2002-08-05

Family

ID=17886641

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30058791A Expired - Lifetime JP3311371B2 (en) 1991-04-01 1991-11-15 Cushioning material

Country Status (1)

Country Link
JP (1) JP3311371B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6194483B1 (en) 1998-08-31 2001-02-27 Kimberly-Clark Worldwide, Inc. Disposable articles having biodegradable nonwovens with improved fluid management properties
US6197860B1 (en) 1998-08-31 2001-03-06 Kimberly-Clark Worldwide, Inc. Biodegradable nonwovens with improved fluid management properties
US6195975B1 (en) 1997-08-28 2001-03-06 Belmont Textile Machinery Co., Inc. Fluid-jet false-twisting method and product
US6201068B1 (en) 1997-10-31 2001-03-13 Kimberly-Clark Worldwide, Inc. Biodegradable polylactide nonwovens with improved fluid management properties
US6268434B1 (en) 1997-10-31 2001-07-31 Kimberly Clark Worldwide, Inc. Biodegradable polylactide nonwovens with improved fluid management properties
US6306782B1 (en) 1997-12-22 2001-10-23 Kimberly-Clark Worldwide, Inc. Disposable absorbent product having biodisintegratable nonwovens with improved fluid management properties
US6309988B1 (en) 1997-12-22 2001-10-30 Kimberly-Clark Worldwide, Inc. Biodisintegratable nonwovens with improved fluid management properties
US6544455B1 (en) 1997-12-22 2003-04-08 Kimberly-Clark Worldwide, Inc. Methods for making a biodegradable thermoplastic composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6195975B1 (en) 1997-08-28 2001-03-06 Belmont Textile Machinery Co., Inc. Fluid-jet false-twisting method and product
US6201068B1 (en) 1997-10-31 2001-03-13 Kimberly-Clark Worldwide, Inc. Biodegradable polylactide nonwovens with improved fluid management properties
US6268434B1 (en) 1997-10-31 2001-07-31 Kimberly Clark Worldwide, Inc. Biodegradable polylactide nonwovens with improved fluid management properties
US6475418B1 (en) 1997-10-31 2002-11-05 Kimberly-Clark Worldwide, Inc. Methods for making a thermoplastic composition and fibers including same
US6306782B1 (en) 1997-12-22 2001-10-23 Kimberly-Clark Worldwide, Inc. Disposable absorbent product having biodisintegratable nonwovens with improved fluid management properties
US6309988B1 (en) 1997-12-22 2001-10-30 Kimberly-Clark Worldwide, Inc. Biodisintegratable nonwovens with improved fluid management properties
US6544455B1 (en) 1997-12-22 2003-04-08 Kimberly-Clark Worldwide, Inc. Methods for making a biodegradable thermoplastic composition
US6194483B1 (en) 1998-08-31 2001-02-27 Kimberly-Clark Worldwide, Inc. Disposable articles having biodegradable nonwovens with improved fluid management properties
US6197860B1 (en) 1998-08-31 2001-03-06 Kimberly-Clark Worldwide, Inc. Biodegradable nonwovens with improved fluid management properties
US6245831B1 (en) 1998-08-31 2001-06-12 Kimberly-Clark Worldwide, Inc. Disposable articles having biodegradable nonwovens with improved fluid management properties

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