JP2006070178A - Biodegradable foam container - Google Patents
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Abstract
Description
本発明は、生分解性発泡容器に関し、更に詳しくは、直接地中に埋設可能または廃棄時にサーマルリサイクル、コンポスト、バイオガス等の方法でリサイクル可能であり、土壌埋設や微生物処理時に生分解速度が速く、軽量で強度があり、断熱性を有する、樹木、種苗育成用の生分解性発泡容器に関する。 The present invention relates to a biodegradable foam container, and more specifically, it can be buried directly in the ground or can be recycled by a method such as thermal recycling, compost, biogas at the time of disposal, and has a biodegradation rate when buried in soil or treated with microorganisms. The present invention relates to a biodegradable foam container for growing trees and seedlings that is fast, lightweight, strong, and has heat insulation properties.
従来、発泡容器としては、発泡スチレン系合成樹脂が使用されているが、これらは使用後に廃棄物となるために、その処理が問題となっていた。その改善方法としては発泡スチレン系合成樹脂にわら等を加えた材料によって作成されているものが知られている(例えば、特許文献1参照。)。しかしながら、これらの材料は、サーマルリサイクルのみでしかリサイクルできず、しかも使用中劣化・破壊したものは土壌に拡散し、環境を汚染することが懸念される。
また、リサイクル性、環境への負荷等を考慮して、オール生分解性の素材で作られている容器も知られている。例えば、生分解性脂肪族ポリエステル樹脂と紙粉からなり、苗木等のポットごとそのまま土中に移植できる植生ポット(例えば、特許文献2参照。)や、もみ殻と生分解性プラスチックを加熱・加圧プレスして作成した容器(例えば、特許文献3参照。)が知られている。これらの容器は、植物材料や生分解性樹脂を利用した点では、リサイクル性も良く、強度もある程度確保できる。しかしながら、これらの容器は、取り扱い時の強度が弱く、苗を植えるときや、ハンドリングの際に、衝撃で割れやすいという欠点があるばかりでなく、使用中に強度低下が大きく壊れやすい欠点がある。また、土壌にそのまま埋めても、分解性が遅く、苗の根の生育を阻害する可能性があり、廃棄時にコンポストや微生物処理する場合に分解し難いという問題がある。
In addition, containers made of all biodegradable materials are also known in consideration of recyclability and environmental burden. For example, a vegetation pot made of biodegradable aliphatic polyester resin and paper powder, which can be transplanted into the soil as it is with a pot of seedlings (see, for example, Patent Document 2), rice husk and biodegradable plastic are heated and added. A container (see, for example, Patent Document 3) created by pressure pressing is known. These containers have good recyclability and can secure a certain degree of strength in terms of using plant materials and biodegradable resins. However, these containers are weak in handling and have the disadvantage that they are easily broken by impact when planting seedlings and handling, and also have the disadvantage that the strength is greatly reduced during use. Moreover, even if it is buried in the soil as it is, there is a problem that it is slow to decompose and may hinder the growth of seedling roots, and it is difficult to decompose when it is composted or treated with microorganisms at the time of disposal.
本発明は、上記問題点に鑑み、軽量で、取り扱い時の強度が強く、使用中の強度低下が小さく、土壌にそのまま埋めても分解性が早く、苗の根の生育を阻害せず、また、廃棄時にコンポストや微生物処理する場合に分解し易い生分解性発泡容器を提供することを目的とする。 In view of the above problems, the present invention is light in weight, strong in handling, small in strength reduction during use, is quick to decompose even if buried in soil as it is, and does not inhibit the growth of seedling roots. An object of the present invention is to provide a biodegradable foam container that is easily decomposed when composting or microbial treatment at the time of disposal.
本発明者らは、上記課題を解決すべく鋭意検討を重ねた結果、生分解性樹脂と有機化層状ケイ酸塩を含有する樹脂組成物を炭酸ガス等により発泡成形した容器は、軽量、かつ使用時の強度、形状保持等の機械物性、断熱性、土壌埋設時の分解性に優れた生分解性の発泡容器となり、特に、通常使用状態での耐久性に優れ、容器に植生土壌を入れて苗を育成する間は生分解せず、土壌に埋設した後では、問題なく分解する発泡容器が得られることを見出し本発明を完成させた。 As a result of intensive studies to solve the above-mentioned problems, the present inventors have obtained a lightweight and lightweight container formed by foaming a resin composition containing a biodegradable resin and an organically modified layered silicate with carbon dioxide gas, etc. It becomes a biodegradable foam container with excellent mechanical properties such as strength during use, shape retention, thermal insulation, and degradability when buried in soil, and is particularly durable in normal use conditions. The present invention has been completed by finding that a foamed container that does not biodegrade during seedling growth and can be decomposed without problems after being embedded in soil.
すなわち、本発明の第1の発明によれば、生分解性樹脂と有機化層状ケイ酸塩を含有する樹脂組成物からなる生分解性発泡容器であって、容器の密度が0.2〜0.85g/cm3であることを特徴とする生分解性発泡容器が提供される。 That is, according to the first invention of the present invention, a biodegradable foam container comprising a resin composition containing a biodegradable resin and an organically modified layered silicate, wherein the density of the container is 0.2-0. A biodegradable foam container is provided, characterized in that it is .85 g / cm 3 .
また、本発明の第2の発明によれば、第1の発明において、生分解性樹脂が脂肪族ポリエステル系樹脂であることを特徴とする生分解性発泡容器が提供される。 According to a second aspect of the present invention, there is provided a biodegradable foam container according to the first aspect, wherein the biodegradable resin is an aliphatic polyester resin.
また、本発明の第3の発明によれば、第1又は2の発明において、有機化層状ケイ酸塩の配合量が樹脂組成物全体の0.01〜5重量%であることを特徴とする生分解性発泡容器が提供される。 According to the third invention of the present invention, in the first or second invention, the compounding amount of the organically modified layered silicate is 0.01 to 5% by weight of the entire resin composition. A biodegradable foam container is provided.
本発明の生分解性発泡容器は、生分解性樹脂と有機化層状ケイ酸塩を含有する樹脂組成物からなり、容器の密度が0.2〜0.85g/cm3であるので、土壌中での分解性が促進され、しかも軽量で通常の取り扱い時に割れ等の問題がなく、苗の生育に好適な生分解性発泡容器とすることができる。 The biodegradable foam container of the present invention comprises a resin composition containing a biodegradable resin and an organically modified layered silicate, and the density of the container is 0.2 to 0.85 g / cm 3. The biodegradable foamed container is suitable for growing seedlings because it is lightweight and has no problems such as cracking during normal handling.
本発明は、生分解性樹脂に有機化層状ケイ酸塩を含有する樹脂組成物を発泡成形した生分解性発泡容器である。以下、本発明について詳細を述べる。 The present invention is a biodegradable foam container obtained by foam-molding a resin composition containing an organically modified layered silicate in a biodegradable resin. Hereinafter, the present invention will be described in detail.
1.生分解性樹脂
本発明の生分解性樹脂からなる発泡容器に使用される生分解性樹脂としては、発泡成形可能な生分解性樹脂であればどのようなものでも使用できる。例えば、脂肪族ポリエステル、ポリアミノ酸、ポリアミド/ポリエステル共重合体、ポリペプチド、セルロース、または熱可塑性変成でん粉等が挙げられ、それらからなる群から選ばれる少なくとも一つの樹脂もしくはそれらの誘導体が挙げられる。
これらの中では、特に好ましくは、脂肪族ポリエステルが挙げられ、ポリグリコール酸、ポリ乳酸または乳酸と他のヒドロキシルカルボン酸とのコポリマーあるいはこれらの混合物、ポリ(ε−カプロラクトン)、ポリエチレンサクシネート、ポリテトラメチレンサクシネート、ポリ−β−プロピオラクトン、ポリ−β−ブチロラクトン、ポリ−γ−ブチロラクトン、ポリブチレンサクシネート(PBS)および他のジカルボン酸との共重合物であるL乳酸共重合物(PBSL),カプロン酸共重合物(PBSCL)、ポリブチレンサクシネート−カーボネート、ポリブチレンサクシネート−アジペート、およびこれら脂肪族ポリエステル樹脂のイシソアネート架橋物またはそれら化合物の混合物、脂肪族ポリエステルとポリアミドとの共重合体が用いられる。
本発明に用いられる上記生分解性の脂肪族ポリエステル系樹脂は、どのようなものでも良いが、好ましくはフィルムグレード、発泡グレードに用いられるもの、またはメルトインデックス(MI値)が2〜15のもの、さらに好ましくはひずみ硬化性を発現するものが良い。
1. Biodegradable Resin Any biodegradable resin that can be foam-molded can be used as the biodegradable resin used in the foam container made of the biodegradable resin of the present invention. Examples thereof include aliphatic polyesters, polyamino acids, polyamide / polyester copolymers, polypeptides, celluloses, thermoplastic modified starches, and the like, and at least one resin selected from the group consisting of them or derivatives thereof.
Among these, particularly preferred are aliphatic polyesters such as polyglycolic acid, polylactic acid or copolymers of lactic acid with other hydroxyl carboxylic acids or mixtures thereof, poly (ε-caprolactone), polyethylene succinate, poly L-lactic acid copolymer which is a copolymer of tetramethylene succinate, poly-β-propiolactone, poly-β-butyrolactone, poly-γ-butyrolactone, polybutylene succinate (PBS) and other dicarboxylic acids ( PBSL), caproic acid copolymer (PBSCL), polybutylene succinate-carbonate, polybutylene succinate-adipate, and isothiocyanate cross-linked products of these aliphatic polyester resins or mixtures of these compounds, aliphatic polyester and polyamide copolymer polymerization It is used.
The biodegradable aliphatic polyester-based resin used in the present invention may be any one, but is preferably used for film grade, foam grade, or has a melt index (MI value) of 2 to 15. More preferably, a material exhibiting strain hardening is preferable.
本発明で用いる生分解性樹脂には、さらには、生分解性を損なわない範囲で架橋剤を添加しても良い。架橋剤の添加割合は5%以下が好ましく、これ以上では生分解性が低下すると共に、発泡の気泡成長を妨げる。架橋剤としては、多価カルボン酸、イソシアネート化合物、有機過酸化物、エポキシ化合物、シランカップリング剤、金属錯体等またはシェラック、ひまし油等の天然の熱硬化成分などが用いられる。 A cross-linking agent may be added to the biodegradable resin used in the present invention as long as the biodegradability is not impaired. The addition ratio of the crosslinking agent is preferably 5% or less, and if it is more than this, the biodegradability is lowered and the bubble growth of the foam is hindered. As the crosslinking agent, a polyvalent carboxylic acid, an isocyanate compound, an organic peroxide, an epoxy compound, a silane coupling agent, a metal complex, or a natural thermosetting component such as shellac or castor oil is used.
2.有機化層状ケイ酸塩
本発明で用いる層状ケイ酸塩とは、層間に交換性陽イオンを有する珪酸塩鉱物を意味し、通常、厚さが約1nm、平均アスペクト比がおよそ20〜200程度の微細な薄片状結晶がイオン結合により凝集してなるものである。
層状珪酸塩の種類は、特に限定されず、モンモリロナイト、サポナイト、ヘクトライト、バイデライト、スティブンサイト、ノントロナイトなどのスメクタイト系粘土鉱物のほか、バーミキュライト、ハロイサイト、及び膨潤性マイカなどが挙げられ、天然のものでも合成されたものでも用いることが出来る。
2. Organized layered silicate The layered silicate used in the present invention means a silicate mineral having exchangeable cations between layers, and usually has a thickness of about 1 nm and an average aspect ratio of about 20 to 200. Fine flaky crystals are aggregated by ionic bonds.
The type of layered silicate is not particularly limited, and examples include smectite clay minerals such as montmorillonite, saponite, hectorite, beidellite, stevensite, nontronite, vermiculite, halloysite, and swellable mica. Either natural or synthesized can be used.
本発明おける有機化層状ケイ酸塩は、上記層状ケイ酸塩をカチオン系界面活性剤により処理したものである。カチオン系界面活性剤としては、特に限定されるものではないが、4級アンモニウム塩、4級ホスホニウム塩等が挙げられ、好ましくは炭素数8以上のアルキル鎖を有する4級アンモニウム塩が用いられる。炭素数が8以上のアルキル鎖を含有しない場合には,アルキルアンモニウムイオンの親水性が強く、層状珪酸塩の層間を十分に非極性化することが困難となり、生分解性樹脂、特に脂肪族ポリエステル系生分解性樹脂との分散性が低下し、発泡性が低下する。 The organically modified layered silicate in the present invention is obtained by treating the above layered silicate with a cationic surfactant. Although it does not specifically limit as a cationic surfactant, A quaternary ammonium salt, a quaternary phosphonium salt, etc. are mentioned, Preferably the quaternary ammonium salt which has a C8 or more alkyl chain is used. When the alkyl chain having 8 or more carbon atoms is not contained, the hydrophilicity of the alkylammonium ion is strong and it becomes difficult to sufficiently depolarize the layer of the layered silicate, and biodegradable resin, particularly aliphatic polyester Dispersibility with the system biodegradable resin is lowered, and foamability is lowered.
4級アンモニウム塩としては、例えば、ラウリルトリメチルアンモニウム塩、ステアリルトリメチルアンモニム塩、トリオクチルアンモニウム塩、ジステアリルジメチルアンモニウム塩(以下、DSDMと略記する場合がある)、ジ硬化牛脂ジメチルアンモニウム塩、ジステアリルジベンジルアンモニウム塩等が挙げられる。 Examples of the quaternary ammonium salt include lauryl trimethyl ammonium salt, stearyl trimethyl ammonium salt, trioctyl ammonium salt, distearyl dimethyl ammonium salt (hereinafter sometimes abbreviated as DSDM), di-cured tallow dimethyl ammonium salt, di Examples include stearyl dibenzylammonium salt.
また、ケイ酸塩の層間に銀イオンを配位したものでもよい。さらに、場合によっては生分解性樹脂との密着性をあげるために有機化層状ケイ酸塩をシランカップリング剤やチタネート系のカップリング剤で処理したものを用いても良い。 Alternatively, silver ions may be coordinated between silicate layers. Further, in some cases, an organically modified layered silicate treated with a silane coupling agent or a titanate-based coupling agent may be used in order to improve adhesion to the biodegradable resin.
本発明において使用される有機化層状ケイ酸塩の含有量は、樹脂組成物全体量の0.05〜5重量%が好ましく、特に好ましくは0.5〜3重量%である。土壌埋設後の分解性が良好で、埋設前の苗を生育する段階での分解性低下、強度保持、容器の発泡倍率(軽量性)の観点から含有量が0.05〜5重量%であるものが好ましい。
有機化層状ケイ酸塩の含有量が0.05重量%未満の場合は、生分解性樹脂の分解速度と同じで土壌の埋設前でも容器内の植生土壌により徐々に分解され、埋設時には物性低下しハンドリング時に衝撃により壊れやすくなっている。5重量%を超えると、容器発泡成形時の発泡性が大きく低下し、軽量性が確保できなくなる。また、含有量が大きくなると逆に容器の耐衝撃性が極端に低下して、通常のハンドリング時でも壊れやすくなる。分解速度も土壌に埋設後の分解が大きく低下するという不具合が生じる。
The content of the organically modified layered silicate used in the present invention is preferably 0.05 to 5% by weight, particularly preferably 0.5 to 3% by weight, based on the total amount of the resin composition. Degradability after soil embedding is good, and the content is 0.05 to 5% by weight from the viewpoint of degradability degradation at the stage of growing seedlings before embedding, strength retention, and foam expansion ratio (lightness) of the container Those are preferred.
When the organic layered silicate content is less than 0.05% by weight, the degradation rate of the biodegradable resin is the same as that of the biodegradable resin. However, it is fragile due to impact during handling. If it exceeds 5% by weight, the foamability at the time of container foam molding is greatly reduced, and the lightness cannot be secured. On the other hand, when the content is increased, the impact resistance of the container is extremely reduced, and the container is easily broken even during normal handling. There is a problem that the decomposition rate is greatly reduced after being buried in the soil.
3.その他の成分
本発明には、必要に応じて、植物性の繊維を混合してもよい。例えば、スギ、ヒノキ、マツ等の木材の粉末や繊維、または非木質系繊維のケナフ、ジュート、亜麻、ラミー、葦等の靱皮繊維、綿花、カポック等の種子由来繊維、マニラ麻、サイザル麻等の茎または葉の繊維、シュロ繊維等の幹繊維、ここやし繊維等の果実殻繊維および竹、笹繊維等を単一または複数混合しても良い。含有量や、繊維の大きさ等は発泡性が低下しない程度に目的とする強度と分解の程度に応じて決定するのが良い。
3. Other components In this invention, you may mix a vegetable fiber as needed. For example, wood powders and fibers of cedar, cypress, pine, etc., bast fibers such as kenaf, jute, flax, ramie, cocoon of non-wood fibers, cotton, seed fibers such as kapok, manila hemp, sisal hemp, etc. Stem or leaf fibers, stem fibers such as palm fibers, fruit shell fibers such as palm fibers, and bamboo or straw fibers may be used singly or in combination. The content, the size of the fiber, and the like are preferably determined in accordance with the target strength and the degree of decomposition to such an extent that foamability is not lowered.
また、発泡性や強度を調整するために、他の天然の無機成分を用いても良く、例えば、タルク、炭酸カルシウム、酸化カルシウムや石灰や貝殻粉砕物またはこれらの焼成物を添加しても良い。そのた、粘土鉱物、粒状シリカ化合物、酸化チタン、炭、ゼオライト化合物、珪藻土やこれらを有機シランカップリング処理したものでも構わない。添加量としては原料や形状により異なるが、発泡性や分解性を低下させないためには10重量%以下が好ましい。 Moreover, in order to adjust foamability and intensity | strength, you may use another natural inorganic component, for example, you may add a talc, a calcium carbonate, a calcium oxide, lime, shell pulverized materials, or these baked products. . In addition, clay minerals, granular silica compounds, titanium oxide, charcoal, zeolite compounds, diatomaceous earth, and those obtained by organic silane coupling treatment may be used. The amount added varies depending on the raw material and shape, but is preferably 10% by weight or less so as not to lower the foamability and decomposability.
さらにまた、生分解性樹脂の分解性を調整するために植物繊維やアセチル化処理等の繊維の表面処理を行った植物繊維を添加しても良い。また、接着性の改良材として、天然物由来の酢酸セルロース系樹脂や変成でんぷん、ポリアミノ酸系樹脂、ポリアミノ酸とポリエステルの共重合物等を添加しても構わない。 Furthermore, in order to adjust the degradability of the biodegradable resin, plant fibers that have been subjected to surface treatment such as plant fibers or acetylation treatment may be added. Moreover, you may add the cellulose acetate resin derived from a natural product, a modified starch, a polyamino acid resin, the copolymer of a polyamino acid and polyester, etc. as an adhesive improvement material.
4.樹脂組成物
本発明において生分解性樹脂に有機化層状ケイ酸塩を混合して樹脂組成物を製造する方法としては、どのような方法でも良く、あらかじめ両者を混練機により混練して混合物またはペレットを作成した後、これを射出発泡機によって発泡成形する方法や直接射出発泡機に両者を導入し、発泡成形する方法がある。また混練り機や直接射出成形装置に有機化層状ケイ酸塩を導入する場合、前もって生分解性樹脂と有機化層状ケイ酸塩をドライブレンドしたのち装置に導入する方法と別々の導入口より装置に導入して混合する方法がある。
4). Resin composition In the present invention, any method may be used as a method for producing a resin composition by mixing an organically modified layered silicate with a biodegradable resin. There are a method of foam molding using an injection foaming machine and a method of foam molding by directly introducing both into an injection foaming machine. In addition, when introducing an organic layered silicate into a kneader or direct injection molding device, a method of dry blending the biodegradable resin and the organic layered silicate in advance and then introducing the device into the device from a separate inlet There is a method of introducing and mixing.
5.発泡容器
本発明の生分解性発泡容器の形状はどのようなものでも良く、使用する目的によって形状が決定される。苗ポットとして利用する場合は、直径が5〜20cm程度、高さが5〜30cm程度ですり鉢状、コーヒーカップ状など円筒状、円錐状のものが一般的に適用されるが、立方体、直方体の容器、三角錐などどのような形状でも構わない。
また、容器の肉厚は発泡体の成形が容易な3〜15mmが好ましい。さらに、容器の底部や側面には任意に孔、スリット等を設けることができる。例えば、苗ポットとして利用する場合は、底部に直径が2〜10mm程度の水抜きの孔やスリットを数個設けることができる。また、側面にも水抜きの孔やスリットを数個配置することができる。
5. Foaming container The biodegradable foaming container of the present invention may have any shape, and the shape is determined depending on the purpose of use. When used as a seedling pot, the diameter is about 5 to 20 cm and the height is about 5 to 30 cm. Cylindrical shapes such as mortar shapes and coffee cup shapes are generally applied. Any shape such as a container or a triangular pyramid may be used.
The wall thickness of the container is preferably 3 to 15 mm, which facilitates foam molding. Furthermore, a hole, a slit, etc. can be arbitrarily provided in the bottom part or side surface of the container. For example, when using it as a seedling pot, several holes and slits having a diameter of about 2 to 10 mm can be provided at the bottom. Also, several drain holes and slits can be arranged on the side surface.
本発明の発泡容器の密度は、0.2〜0.85g/cm3が好ましく、より好ましくは0.35〜0.6g/cm3である。容器の密度が0.2g/cm3未満であると、苗充填後の容器の強度が不足し、取扱時に容器が破損し易くなり、0.85g/cm3を超えると、軽量性のメリットが出ないばかりでなく、土壌に埋没後の容器の分解性が低下すると共に、通気性が低下するので苗の発育不良の原因となる。 The density of the foamed container of the present invention is preferably 0.2 to 0.85 g / cm 3 , more preferably 0.35 to 0.6 g / cm 3 . When the density of the container is less than 0.2 g / cm 3 , the strength of the container after seedling filling is insufficient, and the container is easily damaged during handling, and when it exceeds 0.85 g / cm 3 , there is a merit of lightness. Not only does not come out, but also the degradability of the container after being buried in the soil is lowered, and the air permeability is lowered, which causes the growth failure of the seedling.
本発明において生分解性の発泡容器の製造方法は、公知の発泡成形方法が適用でき、化学発泡剤を利用する方法、発泡性ガスを利用する方法、および両者を併用する方法のどのような方法でもよいが、好ましくは化学発泡剤を使用せず、炭酸ガスまたは炭酸ガスと窒素ガスの混合ガス、炭酸ガスとブタンまたは低揮発性溶剤を利用する射出発泡成形が適用される。特に好ましくは炭酸ガスのみで発泡する方法がよい。 In the present invention, as a method for producing a biodegradable foam container, a known foam molding method can be applied. Any method of using a chemical foaming agent, a method of using a foaming gas, and a method of using both in combination. However, a chemical foaming agent is preferably used, and injection foam molding using carbon dioxide gas or a mixed gas of carbon dioxide gas and nitrogen gas, carbon dioxide gas and butane, or a low-volatile solvent is applied. A method of foaming only with carbon dioxide gas is particularly preferable.
以下に実施例で本発明を詳細に説明するが、本発明は、実施例に限定されるものではない。 EXAMPLES The present invention will be described in detail below with reference to examples, but the present invention is not limited to the examples.
(実施例1)
原料となる生分解性樹脂として、ポリブチレンサクシネート(三菱化学社製 GSPla)を使用し、有機化層状ケイ酸塩として、メチル基とヒドロキシエチル基を有し、炭素数が18以上のアルキル基を65%以上有する4級アンモニウム塩で処理したモンモリロナイトのクロイサイト30B(ナノコール社製)を用いた。生分解性樹脂と有機化層状ケイ酸塩は、あらかじめ2軸押出装置にて有機化層状ケイ酸塩の配合量が0.5wt%となるように混合し、バレル温度150℃で加熱溶融し、直径が3mm程度のペレットを作成した。次に得られたペレットを射出発泡成形機に導入し、射出速度480mm/s、シリンダー温度170℃、金型温度40℃、ガス圧力7MPa、ガス注入量3.5wt%で発泡射出し、底面の直径70mm、開口部の直径80mm、高さ120mm、肉厚6mmの円筒状の発泡容器を作成した。このときの発泡容器の密度は0.53g/cm3であった。
次に、発泡容器の底部に3mm径の孔28個を開け、植生用の土壌(腐葉土60%、まさ土30%、軽石10%)を充満させ、センリョウを植え、屋外にて一ヶ月栽培後の苗の成長度合いおよび容器の底部の状態を観察した。
また、発泡容器から厚み6mm、幅10mm、長さ20mmの試料片を切り出し標準土壌での生分解性をJISK6953の方法に準拠し、生分解性試験装置MODAにより測定した。この時、設定温度は30℃とし、分解率が20%となる日数を計測した。結果を表1に示す。
Example 1
Polybutylene succinate (GSPla manufactured by Mitsubishi Chemical Co., Ltd.) is used as a raw material biodegradable resin, and an organic layered silicate has a methyl group and a hydroxyethyl group, and an alkyl group having 18 or more carbon atoms. Montmorillonite cloicite 30B (manufactured by Nanocor) treated with a quaternary ammonium salt having 65% or more. The biodegradable resin and the organically modified layered silicate are mixed beforehand in a biaxial extruder so that the blending amount of the organically modified layered silicate is 0.5 wt%, and heated and melted at a barrel temperature of 150 ° C. A pellet having a diameter of about 3 mm was prepared. Next, the obtained pellets were introduced into an injection foam molding machine, and foamed and injected at an injection speed of 480 mm / s, a cylinder temperature of 170 ° C., a mold temperature of 40 ° C., a gas pressure of 7 MPa, and a gas injection amount of 3.5 wt%. A cylindrical foam container having a diameter of 70 mm, an opening diameter of 80 mm, a height of 120 mm, and a wall thickness of 6 mm was prepared. The density of the foamed container at this time was 0.53 g / cm 3 .
Next, 28 holes of 3mm diameter are opened at the bottom of the foam container, filled with vegetation soil (60% humus soil, 30% masa soil, 10% pumice), planted with ginseng, and grown outdoors for one month. The degree of seedling growth and the state of the bottom of the container were observed.
Further, a sample piece having a thickness of 6 mm, a width of 10 mm, and a length of 20 mm was cut out from the foamed container, and the biodegradability in standard soil was measured by a biodegradability test apparatus MODEA in accordance with the method of JIS K6953. At this time, the set temperature was 30 ° C., and the number of days when the decomposition rate was 20% was measured. The results are shown in Table 1.
(実施例2)
実施例1において有機化層状ケイ酸塩の配合量が3wt%となるようにしてペレットを作成し、射出発泡時のシリンダー温度を180℃、ガス注入量を3.2wt%として、射出発泡容器を得た。このとき発泡容器の密度は0.6g/cm3であった。結果を表1に示す。
(Example 2)
In Example 1, pellets were prepared so that the blended amount of the organically modified layered silicate was 3 wt%, the cylinder temperature during injection foaming was 180 ° C., and the gas injection amount was 3.2 wt%. Obtained. At this time, the density of the foamed container was 0.6 g / cm 3 . The results are shown in Table 1.
(実施例3)
実施例1において有機化層状ケイ酸塩として、メチル基を有し、炭素数が18以上のアルキル基を65%以上有する4級アンモニウム塩で処理したモンモリロナイトであるクロイサイト93A含有量が3wt%となるように用いて発泡容器を作成した。このときの発泡容器の密度は0.75g/cm3であった。結果を表1に示す。
(Example 3)
In Example 1, the content of cloisite 93A, which is montmorillonite treated with a quaternary ammonium salt having a methyl group and having an alkyl group having 18 or more carbon atoms of 65% or more, is 3 wt% as the organically modified layered silicate. A foamed container was prepared using the above. The density of the foam container at this time was 0.75 g / cm 3 . The results are shown in Table 1.
(比較例1)
実施例1と同様の生分解性樹脂と成形金型を使用し、射出速度480mm/s、シリンダー温度160℃、金型温度40℃で射出成形し、底面の直径70mm、開口部の直径80mm、高さ120mm、肉厚6mmの円筒状の非発泡の容器を作成した。このときの容器の密度は1.25g/cm3であった。結果を表1に示す。
(Comparative Example 1)
Using the same biodegradable resin and molding die as in Example 1, injection molding was performed at an injection speed of 480 mm / s, a cylinder temperature of 160 ° C., and a mold temperature of 40 ° C., a bottom diameter of 70 mm, an opening diameter of 80 mm, A cylindrical non-foamed container having a height of 120 mm and a wall thickness of 6 mm was prepared. The density of the container at this time was 1.25 g / cm 3 . The results are shown in Table 1.
(比較例2)
実施例1と同様の生分解性樹脂と金型を使用し、射出速度480mm/s、シリンダー温度160℃、金型温度40℃、ガス圧力7MPa、ガス注入量3.5wt%で発泡射出し、底面の直径70mm、開口部の直径80mm、高さ120mm、肉厚6mmの円筒状の発泡容器を作成した。このときの発泡容器の密度は0.48g/cm3であった。結果を表1に示す。
(Comparative Example 2)
Using the same biodegradable resin and mold as in Example 1, the injection speed was 480 mm / s, the cylinder temperature was 160 ° C., the mold temperature was 40 ° C., the gas pressure was 7 MPa, and the gas injection amount was 3.5 wt%. A cylindrical foam container having a bottom diameter of 70 mm, an opening diameter of 80 mm, a height of 120 mm, and a wall thickness of 6 mm was prepared. The density of the foam container at this time was 0.48 g / cm 3 . The results are shown in Table 1.
(比較例3)
実施例1と同様の生分解性樹脂と金型を使用し、有機化層状ケイ酸塩としてクロイサイト30Bを0.03wt%を配合し、射出速度480mm/s、シリンダー温度165℃、金型温度40℃、ガス圧力7MPa、ガス注入量3.5wt%で発泡射出し、底面の直径70mm、開口部の直径80mm、高さ120mm、肉厚6mmの円筒状の発泡容器を作成した。このときの発泡容器の密度は0.48g/cm3であった。結果を表1に示す。
(Comparative Example 3)
The same biodegradable resin and mold as in Example 1 were used, and 0.03 wt% of Closite 30B was blended as an organically modified layered silicate, injection speed 480 mm / s, cylinder temperature 165 ° C., mold temperature Foam injection was performed at 40 ° C., a gas pressure of 7 MPa, a gas injection amount of 3.5 wt%, and a cylindrical foam container having a bottom diameter of 70 mm, an opening diameter of 80 mm, a height of 120 mm, and a wall thickness of 6 mm was prepared. The density of the foam container at this time was 0.48 g / cm 3 . The results are shown in Table 1.
(比較例4)
実施例1において有機化層状ケイ酸塩として、クロイサイト30Bの配合量が6wt%となるようにしてペレットを作成し、射出発泡時のシリンダー温度を180℃、ガス注入量を3.2wt%として、射出発泡容器を得た。このとき発泡容器の密度は1.03g/cm3であった。結果を表1に示す。
(Comparative Example 4)
In Example 1, pellets were prepared so that the compounding amount of closite 30B was 6 wt% as the organic layered silicate, the cylinder temperature at the time of injection foaming was 180 ° C., and the gas injection amount was 3.2 wt%. An injection foam container was obtained. At this time, the density of the foamed container was 1.03 g / cm 3 . The results are shown in Table 1.
表1の結果からわかるように、発泡しない容器に比べて発泡することで土壌中での分解が促進されるが、有機化層状ケイ酸塩を含有することで分解が抑制された。また、土壌に埋設しない通常の保管、育苗期間中では割れ等が無く、通常の取り扱いが可能であった。 As can be seen from the results in Table 1, decomposition in the soil is promoted by foaming compared to a non-foaming container, but decomposition was suppressed by containing an organically modified layered silicate. In addition, there was no cracking during normal storage and seedling periods that were not embedded in soil, and normal handling was possible.
本発明の生分解性発泡容器は、生分解性樹脂と有機化層状ケイ酸塩を含有し、容器の密度が0.2〜0.85g/cm3であるので、土壌中での分解性が抑制され、しかも軽量で通常の取り扱い時に割れ等の問題がないため、水分・微生物が多い環境、例えば堆肥を利用する場合の苗の生育容器として長期間用いることができる。さらに、断熱性に優れ夜間の寒暖の温度変化を受け難く、苗が安定に育ちやすいという特徴を有している。 The biodegradable foam container of the present invention contains a biodegradable resin and an organically modified layered silicate, and the density of the container is 0.2 to 0.85 g / cm 3. Since it is suppressed and is light and free from problems such as cracking during normal handling, it can be used for a long time as a seedling growth container in the case of using an environment with a lot of moisture and microorganisms, for example, compost. Furthermore, it has excellent heat insulation properties, is not easily affected by temperature changes during the night, and has a feature that seedlings are easy to grow stably.
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| JP2004255929A JP2006070178A (en) | 2004-09-02 | 2004-09-02 | Biodegradable foam container |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008101096A (en) * | 2006-10-18 | 2008-05-01 | Aichi Prefecture | POLYLACTIC ACID RESIN COMPOSITION, MOLDED ARTICLE AND METHOD FOR PRODUCING THE SAME |
| WO2010056089A3 (en) * | 2008-11-17 | 2010-08-19 | 제일모직 주식회사 | Clay-reinforced polylactic acid resin composition, a production method for the same, and a moulded article using the same |
| CN101717475B (en) * | 2008-10-09 | 2011-09-14 | 中国科学院化学研究所 | Biodegradable foam plastic and preparation method thereof |
-
2004
- 2004-09-02 JP JP2004255929A patent/JP2006070178A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008101096A (en) * | 2006-10-18 | 2008-05-01 | Aichi Prefecture | POLYLACTIC ACID RESIN COMPOSITION, MOLDED ARTICLE AND METHOD FOR PRODUCING THE SAME |
| CN101717475B (en) * | 2008-10-09 | 2011-09-14 | 中国科学院化学研究所 | Biodegradable foam plastic and preparation method thereof |
| WO2010056089A3 (en) * | 2008-11-17 | 2010-08-19 | 제일모직 주식회사 | Clay-reinforced polylactic acid resin composition, a production method for the same, and a moulded article using the same |
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