Qi Jin, Zhu Kai, Li Ming, Liu Yucan, Duan Pingzhou, Huang Lihua
College of Resources and Environment, Linyi University, Linyi 276000, China.
School of Civil Engineering, Yantai University, Yantai 264005, China.
Molecules. 2025 Jul 30;30(15):3194. doi: 10.3390/molecules30153194.
Steel pickling sludge serves as a valuable iron source for synthesizing Fe-based catalysts in heterogeneous advanced oxidation processes (AOPs). Here, MoS@CoFeO catalyst derived from steel pickling sludge was prepared via a facile solvothermal approach and utilized to activate peroxymonosulfate (PMS) for tetracycline hydrochloride (TCH) degradation. Comprehensive characterization using scanning electron microscopy (SEM)-energy dispersive spectrometer (EDS), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD) confirmed the supported microstructure, composition, and crystalline structure of the catalyst. Key operational parameters-including catalyst dosage, PMS concentration, and initial solution pH-were systematically optimized, achieving 81% degradation efficiency within 30 min. Quenching experiments and electron paramagnetic resonance (EPR) analysis revealed SO as the primary oxidative species, while the catalyst maintained high stability and reusability across cycles. TCH degradation primarily occurs through hydroxylation, decarbonylation, ring-opening, and oxidation reactions. This study presents a cost-effective strategy for transforming steel pickling sludge into a high-performance Fe-based catalyst, demonstrating its potential for practical AOP applications.
钢酸洗污泥是多相高级氧化工艺(AOPs)中合成铁基催化剂的宝贵铁源。在此,通过简便的溶剂热法制备了源自钢酸洗污泥的MoS@CoFeO催化剂,并将其用于活化过一硫酸盐(PMS)以降解盐酸四环素(TCH)。使用扫描电子显微镜(SEM)-能量色散光谱仪(EDS)、X射线光电子能谱(XPS)和X射线衍射(XRD)进行的综合表征证实了催化剂的负载微观结构、组成和晶体结构。对包括催化剂用量、PMS浓度和初始溶液pH值在内的关键操作参数进行了系统优化,在30分钟内实现了81%的降解效率。淬灭实验和电子顺磁共振(EPR)分析表明SO是主要的氧化物种,同时该催化剂在多个循环中保持了高稳定性和可重复使用性。TCH的降解主要通过羟基化、脱羰、开环和氧化反应发生。本研究提出了一种将钢酸洗污泥转化为高性能铁基催化剂的经济有效策略,证明了其在实际AOP应用中的潜力。