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实验室模拟光照辐照揭示了原生大型塑料对风化的强抵抗力。

Laboratory-Simulated Photoirradiation Reveals Strong Resistance of Primary Macroplastics to Weathering.

机构信息

The University of Texas at Austin─Marine Science Institute, Port Aransas, Texas 78373, United States.

Coastal Ocean Vision, North Falmouth, Massachusetts 02556, United States.

出版信息

Environ Sci Technol. 2024 Aug 20;58(33):14775-14785. doi: 10.1021/acs.est.3c09891. Epub 2024 Aug 6.

Abstract

The photodegradation of macroplastics in the marine environment remains poorly understood. Here, we investigated the weathering of commercially available plastics (tabs 1.3 × 4.4 × 0.16 cm), including high-density polyethylene, low-density polyethylene, polypropylene, polystyrene, and polycarbonate, in seawater under laboratory-simulated ultraviolet A radiation for 3-9 months, equivalent to 25-75 years of natural sunlight exposure without considering other confounding factors. After the exposure, the physical integrity and thermal stability of the tabs remained relatively intact, suggesting that the bulk polymer chains were not severely altered despite strong irradiation, likely due to their low specific surface area. In contrast, the surface layer (∼1 μm) of the tabs was highly oxidized and eroded after 9 months of accelerated weathering. Several antioxidant additives were identified in the plastics through low temperature pyrolysis coupled with gas chromatography/mass spectrometry (Pyr-GC/MS) analysis. The Pyr-GC/MS results also revealed many new oxygen-containing compounds formed during photodegradation, and these compounds indicated the dominance of chain scission reactions during weathering. These findings highlight the strong resistance of industrial macroplastics to weathering, emphasizing the need for a broader range of plastics with varying properties and sizes to accurately estimate plastic degradation in the marine environment.

摘要

在海洋环境中,大块塑料的光降解仍然知之甚少。在这里,我们研究了在实验室模拟的紫外线 A 辐射下,海水中包括高密度聚乙烯、低密度聚乙烯、聚丙烯、聚苯乙烯和聚碳酸酯在内的市售塑料(薄片 1.3×4.4×0.16 厘米)经过 3-9 个月的风化作用,相当于在不考虑其他混杂因素的情况下,自然阳光暴露 25-75 年。暴露后,薄片的物理完整性和热稳定性相对完整,这表明尽管受到强烈的辐射,但大块聚合物链并没有受到严重的改变,这可能是由于其比表面积低。相比之下,在加速风化 9 个月后,薄片的表面层(约 1μm)高度氧化和侵蚀。通过低温热解与气相色谱/质谱联用(Pyr-GC/MS)分析,在塑料中鉴定出几种抗氧化添加剂。Pyr-GC/MS 结果还表明,在光降解过程中形成了许多新的含氧化合物,这些化合物表明在风化过程中主要发生了链断裂反应。这些发现强调了工业用大块塑料对风化的强烈抵抗力,这表明需要更广泛的具有不同性质和尺寸的塑料来准确估计海洋环境中的塑料降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26fa/11339922/95cf23abf070/es3c09891_0001.jpg

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