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Biodegradability of conventional and bio-based plastics and natural fiber composites during composting, anaerobic digestion and long-term soil incubation

机译:常规和生物基塑料以及天然纤维复合材料在堆肥,厌氧消化和长期土壤培养过程中的生物降解性

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Plastics are a major constituent of municipal solid waste that pose a growing disposal and environmental pollution problem due to their recalcitrant nature. To reduce their environmental impacts and allow them to be transformed during organic waste recycling processes, various materials have recently been introduced to improve the biodegradability of plastics. These include conventional plastics amended with additives that are meant to enhance their biodegradability, bio-based plastics and natural fiber composites. In this study, the rate and extent of mineralization of a wide range of commercially available plastic alternative materials were determined during composting, anaerobic digestion and soil incubation. The biodegradability was assessed by measuring the amount of carbon mineralized from these materials during incubation under conditions that simulate these three environments and by examination of the materials by scanning electron micrography (SEM). The results showed that during a 660 day soil incubation, substantial mineralization was observed for polyhydroxyalkanoate plastics, starch-based plastics and for materials made from compost. However, only a polyhydroxyalkanoate-based plastic biodegraded at a rate similar to the positive control (cellulose). No significant degradation was observed for polyethylene or polypropylene plastics or the same plastics amended with commercial additives meant to confer biodegradability. During anaerobic digestion for 50 days, 20-25% of the bio-based materials but less than 2% of the additive containing plastics were converted to biogas (CH_4 + CO_2). After 115 days of composting, 0.6% of an additive amended polypropylene, 50% of a plas-tarch material and 12% of a soy wax permeated paper pulp was converted to carbon dioxide. SEM analysis showed substantial disintegration of polyhydroxyalkanoate-based plastic, some surface changes for other bio-based plastics and coconut coir materials but no evidence of degradation of polypropylene or polypropylene containing additives. Although certain bio-based plastics and natural fibers biodegraded to an appreciable extent in the three environments, only a polyhydroxyalkanoate-based resin biodegraded to significant extents during the time scale of composting and anaerobic digestion processes used for solid waste management.
机译:塑料是城市固体废物的主要成分,由于其顽强的性质,导致其处置和环境污染问题日益严重。为了减少它们对环境的影响并允许它们在有机废物回收过程中进行转化,最近引入了各种材料来改善塑料的生物降解性。这些包括常规塑料和旨在增强其生物降解性的添加剂,生物基塑料和天然纤维复合材料。在这项研究中,在堆肥,厌氧消化和土壤培养过程中确定了多种可商购的塑料替代材料的矿化速率和程度。通过在模拟这三种环境的条件下温育期间测量从这些材料中矿化的碳量,并通过扫描电子显微镜(SEM)检查材料,来评估生物降解性。结果表明,在660天的土壤培养中,聚羟基链烷酸酯塑料,淀粉基塑料和由堆肥制成的材料均观察到大量矿化作用。然而,仅基于聚羟基链烷酸酯的塑料以类似于阳性对照(纤维素)的速率生物降解。对于聚乙烯或聚丙烯塑料或用商业添加剂改性的具有赋予生物降解性的相同塑料,未观察到明显的降解。在厌氧消化50天期间,将20-25%的生物基材料转化为沼气(CH_4 + CO_2),但少于2%的含塑料添加剂。堆肥115天后,将0.6%的添加剂改性聚丙烯,50%的增塑剂和12%的大豆蜡渗透纸浆转化为二氧化碳。 SEM分析显示,基于聚羟基链烷酸酯的塑料会大量崩解,其他生物基塑料和椰子椰壳材料的表面也会发生一些变化,但没有证据表明聚丙烯或含聚丙烯的添加剂会降解。尽管某些生物基塑料和天然纤维在这三种环境中会发生一定程度的生物降解,但在用于固体废物管理的堆肥和厌氧消化过程中,只有聚羟基链烷酸酯基树脂会发生很大程度的生物降解。

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