College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610066, PR China; Collaborative Innovation Center for Advanced Nuclear Energy Technology (INET) Tsinghua University, Beijing 100084, PR China.
Collaborative Innovation Center for Advanced Nuclear Energy Technology (INET) Tsinghua University, Beijing 100084, PR China.
Chemosphere. 2024 Apr;353:141586. doi: 10.1016/j.chemosphere.2024.141586. Epub 2024 Mar 5.
Heterogeneous activation of peroxomonosulfate (PMS) has been extensively studied for the degradation of antibiotics. The cobalt ferrite spinel exhibits good activity in the PMS activation, but suffers from the disadvantage of low PMS utilization efficiency. Herein, the nanocomposites including FeS, CoS, CoFeO and FeO were synthesized by hydrothermal method and used for the first time to activate PMS for the removal of sulfamethoxazole (SMX). The nanocomposites showed superior catalytic activity in which the SMX could be completely removed at 40 min, 0.1 g L nanocomposites and 0.4 mM PMS with the first order kinetic constant of 0.2739 min. The PMS utilization efficiency was increased by 29.4% compared to CoFeO. Both radicals and non-radicals contributed to the SMX degradation in which high-valent metal oxo dominated. The mechanism analysis indicated that sulfur modification, on one hand, enhanced the adsorption of nanocomposites for PMS, and promoted the redox cycles of Fe/Fe and Co/Co on the other hand. This study provides new way to enhance the catalytic activity and PMS utilization efficiency of spinel cobalt ferrite.
过一硫酸盐(PMS)的多相活化已被广泛研究用于抗生素的降解。尖晶石型钴铁氧体在 PMS 活化中表现出良好的活性,但存在 PMS 利用效率低的缺点。本文首次采用水热法合成了包括 FeS、CoS、CoFeO 和 FeO 的纳米复合材料,并用于活化 PMS 去除磺胺甲恶唑(SMX)。纳米复合材料表现出优异的催化活性,在 40 min、0.1 g·L 纳米复合材料和 0.4 mM PMS 条件下,SMX 可完全去除,一级动力学常数为 0.2739 min。与 CoFeO 相比,PMS 的利用率提高了 29.4%。自由基和非自由基都有助于 SMX 的降解,其中高价金属氧自由基起主导作用。机理分析表明,硫修饰一方面增强了纳米复合材料对 PMS 的吸附,另一方面促进了 Fe/Fe 和 Co/Co 的氧化还原循环。本研究为提高尖晶石型钴铁氧体的催化活性和 PMS 利用率提供了新途径。