Solar light induced photocatalytic degradation of sulfamethoxazole by ZnWO4/CNNs nanocomposites

降级(电信) 光催化 纳米复合材料 磺胺甲恶唑 材料科学 化学工程 光化学 化学 复合材料 计算机科学 有机化学 催化作用 抗生素 工程类 电信 生物化学
作者
V. Faka,M. Griniezaki,G. Kiriakidis,Eleni Grilla,Dionissios Mantzavinos,Samuel S. Mao,Shaohua Shen,Zacharias Frontistis,Vassiliοs Binas
出处
期刊:Journal of Photochemistry and Photobiology A-chemistry [Elsevier BV]
卷期号:432: 114108-114108 被引量:8
标识
DOI:10.1016/j.jphotochem.2022.114108
摘要

• ZnWO 4 /CNNs nanocomposites were successfully prepared by a simple process. • Sulfamethoxazole was effectively photodegraded by ZnWO 4 /CNNs nanocomposites under solar light illumination. • 30% ZnWO 4 /CNNs nanocomposite exhibits higher photoactivities. • Durability tests of the 30% ZnWO 4 /CNNs photocatalysts have confirmed its excellent recyclability after 5 cycles. The preparation of ZnWO 4 /CNNs nanocomposites was achieved through a simple method at room temperature. In order to investigate the optimum loading of carbon nitride nanosheets (CNNs) for the formation of the nanocomposites, a series of ZnWO 4 /CNNs compositions were prepared and studied through a variety of characterization techniques, such as powder X-ray diffractrometry (pXRD), Scanning Electron Microscopy (SEM) and UV–vis optical measurements. The photocatalytic activity of the nanocomposites was investigated by using sulfamethoxazole (SMX) as a model pollutant. It was found that the material with 30 wt% ZnWO 4 /CNNs exhibited the higher photocatalytic activity. The photocatalytic mechanism was further investigated using appropriate scavengers (t-ButOH, Kl) or under Argon atmosphere to examine the contribution of the different reactive species in the observed photocatalytic activity. The photogenerated holes and the superoxides produced following the promotion of electrons to the conduction band were the main responsible for pollutant's degradation. The photocatalytic efficiency after five sequential experiments showed only a slightly decreased implied high stability of the synthesized material.

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