School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing, 100083, China; Beijing Key Laboratory on Resource-oriented Treatment of Industrial Pollutants, Beijing, 100083, China.
School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing, 100083, China; Beijing Key Laboratory on Resource-oriented Treatment of Industrial Pollutants, Beijing, 100083, China.
Chemosphere. 2022 Jan;287(Pt 2):132211. doi: 10.1016/j.chemosphere.2021.132211. Epub 2021 Sep 13.
In this study, MoS@Z photocatalysts were synthesized by combining ultrasonic and hydrothermal methods, and used for the degradation of tetracycline. The structure characteristics and photocatalytic degradation mechanism of photocatalysts were also systematically investigated. The obtained MoS@Z-5 exhibits the highest photo-degradation efficiency of tetracycline (87.23%), which is 3.58 times more than alkali-modified zeolite (24.34%) and 1.80 times more than pure MoS (48.53%). Furthermore, the MoS@Z-5 showed significant stability in three times photocatalytic recycles and the removal efficiency only decrease by 9.03%. Crystal structure and micromorphology analysis show modified zeolite with collapsed structure can regulate the morphology of nano-MoS and make MoS appear fault structure, which can expose more active sites. In addition, low Si/Al ratio zeolite increases the hydrophilia of MoS@Z-5. Reactive-species-trapping experiments show that the hole is the main reactive oxidizing species. The superior photo-degradation efficiency is mainly attributed to outstanding hydrophilia, exposure of the edge active sites, and efficient separation of photogenerated charge and holes. A possible photocatalytic mechanism and degradation pathways of tetracycline were proposed. The results indicate that MoS@Z-5 may become an efficient, stable, and promising photocatalyst in tetracycline wastewater treatment.
在这项研究中,通过结合超声和水热法合成了 MoS@Z 光催化剂,并将其用于四环素的降解。还系统地研究了催化剂的结构特征和光催化降解机理。所得的 MoS@Z-5 对四环素的光降解效率最高(87.23%),是碱改性沸石(24.34%)的 3.58 倍,是纯 MoS(48.53%)的 1.80 倍。此外,MoS@Z-5 在三次光催化循环中表现出显著的稳定性,去除效率仅下降 9.03%。晶体结构和微观形貌分析表明,具有坍塌结构的改性沸石可以调节纳米 MoS 的形态,使 MoS 呈现出缺陷结构,从而可以暴露更多的活性位点。此外,低 Si/Al 比沸石增加了 MoS@Z-5 的亲水性。自由基捕获实验表明,空穴是主要的活性氧化物质。优异的光降解效率主要归因于出色的亲水性、边缘活性位点的暴露以及光生载流子和空穴的有效分离。提出了一种可能的光催化机制和四环素的降解途径。结果表明,MoS@Z-5 可能成为处理四环素废水的一种高效、稳定且有前景的光催化剂。