Degradation of naphthalene and anthracene using the CdS/ZnO with enhanced photocatalytic activities

光催化 X射线光电子能谱 反应速率常数 扫描电子显微镜 光化学 纳米复合材料 材料科学 降级(电信) 激进的 可见光谱 核化学 化学 催化作用 化学工程 纳米技术 有机化学 动力学 复合材料 电信 计算机科学 工程类 物理 光电子学 量子力学
作者
Tianjiao Qiu,Guangzhou Chen
出处
期刊:Environmental Technology and Innovation [Elsevier]
卷期号:36: 103741-103741 被引量:3
标识
DOI:10.1016/j.eti.2024.103741
摘要

Naphthalene and anthracene, as two common substances of polycyclic aromatic hydrocarbons (PAHs), have the harmful effects on human health (carcinogenic and mutagenic activity), and it is of great significance to remove them. In this paper, the CdS/ZnO nanocomposites were fabricated by the chemical bath deposition method. Its morphology and structure were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and so on. In addition, the photocatalytic degradation efficiency of naphthalene and anthracene was studied under different experimental conditions, including CdS-loading doses, pH, the dosage of photocatalyst and the initial concentrations of solution. Under the condition of pH 7.5, visible light irradiation and the optimal 4 mg nanocomposite, for 2 mg/L naphthalene solution, a maximum photocatalytic degradation efficiency was 98.75 % after 180 min and the corresponding pseudo-first order rate constant was 0.0214 min−1. Under the condition of pH 7.5, visible light irradiation and the optimal 8 mg nanocomposite, for 2 mg/L anthracene solution, the maximum photocatalytic degradation efficiency was 96.13 % after 300 min, and the rate constant was 0.0118 min−1. The above two rate constants were higher than those of their parent catalysts. Based on the free radical trapping experiments, the photocatalytic mechanism showed that •O2- and h+ were the major active radicals in the degradation process with the type-II heterostructure.
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