Polyethylene and related hydrocarbon polymers ("plastics") are not biodegradable

被引:0
|
作者
Jendrossek, Dieter [1 ]
机构
[1] Univ Stuttgart, Inst Microbiol, Allmandring 31, D-70569 Stuttgart, Germany
关键词
Polyethylene biodegradation; Polystyrene biodegradation; Polyvinylchloride biodegradation; BIO-DEGRADATION; POLYSTYRENE; MINERALIZATION;
D O I
10.1016/j.nbt.2024.08.503
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Research on the biodegradation of polyethylene (PE), polystyrene (PS) and related polymers has become popular and the number of publications on this topic is rapidly increasing. However, there is no convincing evidence that the frequently claimed biodegradability of these so-called "plastics" really exists. Rather, a diffuse definition of the term "biodegradability" has led to the publication of reports showing either marginal weight losses of hydrocarbon polymers by the action of isolated bacterial strains or mechanical disintegration and polymer surface modification in case of hydrocarbon polymer-consuming insect larvae. Most of the data can be alternatively explained by the utilization of polymer impurities/additives, by the utilization of low molecular weight oligomers, and/or by physical fragmentation and subsequent loss of small fragments. Evidence for a (partial) biotic and/or abiotic oxidation of the amorphous polymer fraction and of surface-exposed hydrocarbon side chains is not sufficient to claim that PE is biodegradable. To the best of my knowledge, no report has been so far published in which substantial biodegradation and mineralization of PE or related (long chain length) hydrocarbon polymers to carbon dioxide has been convincingly demonstrated by the determination of the fate of carbon atoms in isotope-labeled polymers. It is disappointing that publications with a critical view on biodegradation of hydrocarbon polymers are not cited in most of these reports. The possibility should be considered that the rapidly expanding research field of hydrocarbon polymer biodegradation is chasing rainbows.
引用
收藏
页码:231 / 238
页数:8
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