Tian Na, Giannakis Stefanos, Akbarzadeh Leila, Hasanvandian Farzad, Dehghanifard Emad, Kakavandi Babak
School of Environmental Studies, China University of Geosciences, Wuhan, 430074, PR China; Universidad Politécnica de Madrid, E.T.S. de Ingenieros de Caminos, Canales y Puertos, Departamento de Ingeniería Civil: Hidráulica, Energía y Medio Ambiente, Unidad Docente Ingeniería Sanitaria, C/ Profesor Aranguren, S/n, ES, 28040, Madrid, Spain.
Universidad Politécnica de Madrid, E.T.S. de Ingenieros de Caminos, Canales y Puertos, Departamento de Ingeniería Civil: Hidráulica, Energía y Medio Ambiente, Unidad Docente Ingeniería Sanitaria, C/ Profesor Aranguren, S/n, ES, 28040, Madrid, Spain.
J Environ Manage. 2023 Mar 1;329:117022. doi: 10.1016/j.jenvman.2022.117022. Epub 2022 Dec 20.
In this study, a ternary ZnO@spinel cobalt ferrite@carbon nanotube magnetic photocatalyst (ZSCF@CNT) was successfully synthesized and used to activate peroxymonosulfate (PMS) for Cefixime (CFX) antibiotic degradation under UVC irradiation. The morphology, optical, structural, and physicochemical properties of ZSCF@CNT were characterized and analyzed by XPS, XRD, FESEM-EDX, TEM, BET, VSM, UV-vis DRS and PL analysis. The results indicated that the ternary ZSCF@CNT photocatalyst exhibited superior catalytic activity on CFX elimination than that of individual components and binary composite catalysts, in which CFX with was rapidly removed under UVC irradiation and PMS. The effect of operational parameters including initial PMS, catalyst, and CFX concentrations and solution pH on the catalytic activity was investigated in detail; the optimal conditions were: pH: 7.0, catalyst: 0.3 g/L, PMS: 3.0 mM, leading to total CFX (10 mg/L) elimination in ∼20 min. Based on the radical scavenger tests, various radicals and non-radical species including sulfate, hydroxyl and superoxide radicals, singlet oxygen and electrons were involved in the ZSCF@CNT/PMS/UVC system. The high surface area, reduced agglomeration formation and excellent separation of photogenerated electron-hole pairs embodied in ZSCF@CNT photocatalyst conferred its superior catalytic activity and stability. The results from the tests in real water matrices revealed that ZSCF@CNT could be a promising photocatalyst to activate PMS for actual aqueous matrices' treatment.
在本研究中,成功合成了一种三元ZnO@尖晶石型钴铁氧体@碳纳米管磁性光催化剂(ZSCF@CNT),并用于在紫外光照射下活化过一硫酸盐(PMS)以降解头孢克肟(CFX)抗生素。通过XPS、XRD、FESEM-EDX、TEM、BET、VSM、UV-vis DRS和PL分析对ZSCF@CNT的形貌、光学、结构和物理化学性质进行了表征和分析。结果表明,三元ZSCF@CNT光催化剂对CFX的去除表现出比单个组分和二元复合催化剂更高的催化活性,其中CFX在紫外光照射和PMS存在下被快速去除。详细研究了初始PMS、催化剂、CFX浓度和溶液pH等操作参数对催化活性的影响;最佳条件为:pH:7.0,催化剂:0.3 g/L,PMS:3.0 mM,在约20分钟内可实现对总CFX(10 mg/L)的去除。基于自由基清除剂测试,ZSCF@CNT/PMS/UVC体系涉及多种自由基和非自由基物种,包括硫酸根、羟基和超氧自由基、单线态氧和电子。ZSCF@CNT光催化剂具有高比表面积、减少团聚形成以及优异的光生电子-空穴对分离性能,赋予了其卓越的催化活性和稳定性。实际水体基质测试结果表明,ZSCF@CNT可能是一种有前景的光催化剂,可用于活化PMS处理实际水体基质。