Synergistic Photocatalysis by α-MoO3 Nanostructures and SWCNT Nanocomposites for Efficient Cross-Linking and Oxidative Degradation of Polystyrene Nanoplastics

材料科学 光催化 拉曼光谱 纳米复合材料 聚苯乙烯 傅里叶变换红外光谱 化学工程 降级(电信) 透射电子显微镜 扫描电子显微镜 纳米颗粒 光降解 光谱学 辐照 纳米技术 复合材料 聚合物 有机化学 催化作用 化学 光学 电信 工程类 计算机科学 物理 量子力学 核物理学
作者
Shivam Singh,Sakshi Kapoor,J. P. Singh
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (31): 40914-40926 被引量:1
标识
DOI:10.1021/acsami.4c06616
摘要

Nanoplastics (NPs) generated from plastic debris weathering pose a significant threat to ecosystems. The ubiquity of plastics driven by their advantageous physical properties, necessitates the development of efficient degradation and removal methods. Polystyrene (PS), a common and hazardous aquatic NP is a long-chain hydrocarbon with alternating phenyl groups. This study investigates the photooxidative degradation of PS NPs under UV light irradiation using synthesized MoO3 nanoflakes, nanobelts, and MoO3/SWCNT nanocomposites. Raman spectroscopy, X-ray diffraction, atomic force microscopy, high-resolution transmission electron microscopy, energy dispersive X-ray, Brunauer–Emmett–Teller, and UV–vis spectroscopy were employed to characterize the photocatalyst. Field emission scanning electron microscopy was used to visualize morphological changes in the spherical PS NPs upon interaction with the photocatalysts. MoO3 nanoflakes acting as a photocatalyst under UV irradiation for 24 h achieved an impressive degradation efficiency exceeding 19%. This treatment significantly reduced the average diameter of PS NPs from 220 to 178 nm. Notably, even higher degradation efficiencies were observed with MoO3 nanobelts and nanocomposites as a complete change in the spherical morphology of PS NPs is observed. Fourier transform infrared spectroscopy elucidated the chemical transformations of PS during degradation. The observed changes in PS NPs structure due to photocatalytic oxidation at different time intervals indicate a promising approach.
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