光催化
降级(电信)
化学
可见光谱
煤
化学工程
异质结
核化学
光化学
材料科学
催化作用
有机化学
计算机科学
光电子学
电信
工程类
作者
Hanxuan Zeng,Haojie Zhang,Lin Deng,Zhou Shi
标识
DOI:10.1016/j.jwpe.2019.101084
摘要
CoAl-LDH/g-C3N4 (CoAl-LDH/CN) heterostructures was prepared through self-assembly method using exfoliated CoAl-LDH and g-C3N4 nanosheets via electrostatic attraction force. The morphology and physicochemical properties characterization verified the success synthesis of layer-by-layer structure of CoAl-LDH/CN. Heterogeneous catalytic degradation of sulfadiazine (SDZ) was assessed using CoAl-LDH/CN combined with peroxymonosulfate (PMS) and visible light irradiation. A remarkable synergistic effect was obtained in SDZ removal. After 15 min, 10 μM SDZ could be removed by 87.1 % at conditions of 0.1 g/L CoAl-LDH/CN, 0.5 mM PMS, and pH = 6.0. The reusability tests signified the excellent reusing potential of CoAl-LDH/CN. Mechanism study suggested that CoAl-LDH in the heterostructures activated PMS to produce SO4– and OH, while g-C3N4 acted as dual roles: electron acceptor and PMS activator. Additionally, density functional theory (DFT) calculations successfully disclosed that the sites with high Fukin index (f0) on SDZ molecule were more vulnerable to radicals attack. Eco-toxicity evaluation signified the generation of less toxic intermediates compared to SDZ after photocatalysis. Our findings demonstrate the integration of CoAl-LDH/CN, visible light and PMS can be applied as a promising approach for efficient degradation of organic compound polluted water.
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