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Insights into the degradation mechanism of PET and PP under marine conditions using FTIR

傅里叶变换红外光谱 聚对苯二甲酸乙二醇酯 聚丙烯 降级(电信) 微塑料 聚乙烯 材料科学 扫描电子显微镜 环境科学 化学工程 环境化学 化学 复合材料 计算机科学 工程类 电信
作者
Sarra N. Dimassi,John Ν. Hahladakis,Mohamed Néjib Daly Yahia,Mohammad I. Ahmad,Sami Sayadi,Mohammad A. Al‐Ghouti
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:447: 130796-130796 被引量:51
标识
DOI:10.1016/j.jhazmat.2023.130796
摘要

Plastics possess diverse functional properties that have made them extremely desirable. However, due to poor waste management practices, large quantities eventually end up in the oceans where their degradation begins. Hence, it is imperative to understand and further investigate the dynamics of this process. Currently, most relevant studies have been carried out under benign and/or controlled weather conditions. This study investigates the natural degradation of polypropylene (PP) and polyethylene terephthalate (PET) in more extreme environments. Simulated and real marine conditions, both in the laboratory (indoors) and outdoors were applied for a duration of 140 days and results were assessed using Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) with energy dispersive X-ray analysis. SEM micrographs revealed variations in the morphologies of both plastic types. Degradation signs were shown in both plastic types, under all conditions. Findings indicated that microplastics (MPs) degraded faster than macroplastics, with PP MPs having higher weight loss (49%) than PET MPs (1%) when exposed to outdoor marine conditions. Additionally, the degradation rates of MPs-PP were higher than MPs-PET for outdoor and indoor treatments, with 1.07 × 10-6 g/d and 4.41 × 10-7 g/d, respectively. FTIR combined with PCA was efficient in determining the most degraded plastic types.
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