Synthesis of g-C3N4-based photocatalysts with recyclable feature for efficient 2,4-dichlorophenol degradation and mechanisms

光催化 吸附 2,4-二氯苯酚 降级(电信) 化学 材料科学 双酚A 化学工程 表面光电压 催化作用 光化学 有机化学 光谱学 电信 物理 量子力学 生物 细菌 计算机科学 环氧树脂 遗传学 工程类
作者
Mingna Chu,Kang Hu,Jinshuang Wang,Yanduo Liu,Sharafat Ali,Chuanli Qin,Liqiang Jing
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:243: 57-65 被引量:109
标识
DOI:10.1016/j.apcatb.2018.10.008
摘要

Abstract It is highly desired to produce more O2− by regulating photogenerated electrons for efficiently degrading organic pollutants with recyclable feature. In this work, g-C3N4/active carbon fiber (ACF) photocatalysts with high activities for degrading 2,4-dichlorophenol (2,4-DCP) and bisphenol A (BPA) have been successfully fabricated via an in-situ thermal polycondensation method, attributed to the enhanced charge separation and promoted reactant adsorption from ACF. Moreover, the photocatalytic activities of optimized g-C3N4/ACF photocatalyst could be improved by introducing the carbon layer between them, especially for the nickel-regulated one. It is attributed to the promoted charge transfer and separation by improving the interface contacts between g-C3N4 and ACF, and the function of introduced Ni species to O2 activation, mainly based on the fluorescence spectra related to the formed hydroxyl radical amounts, and the electrochemical oxygen reduction. Furthermore, the photocatalytic activities could be further improved by modifying phosphoric acid to promote the capture of photogenerated electrons by the increased adsorbed oxygen based on the O2 temperature-programmed desorption curves. Interestingly, it is shown that the optimal photocatalyst exhibits 10-time higher photocatalytic activities for 2,4-DCP degradation compared to bare g-C3N4. It is demonstrated through the radical-trapping experiments that O2− is the dominant active species to induce the degradation of 2,4-DCP, along with a suggested decomposition pathway according to the detected main intermediates. This further verifies this point that the photocatalytic activities for degrading organic pollutants could be efficiently improved by mediating electrons. As for the ACF-supported photocatalysts, a specific device has been designed to efficiently purify polluted water with convenient and continuous features. This work opens up a feasible route to develop a high-efficiency photocatalytic technology for recyclable degradation of environmental contaminants.

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