Guangzhou Key Laboratory Environmental Catalysis and Pollution Control, Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control, School of Environmental Science and Engineering, Institute of Environmental Health and Pollution Control, Guangdong University of Technology, Guangzhou 510006, China.
Guangdong Province Solid Waste Recycling and Heavy Metal Pollution Control Engineering Technology Research Center, Guangdong Polytechnic of Environmental Protection Engineering, Foshan 528216, China.
J Hazard Mater. 2022 Jul 5;433:128768. doi: 10.1016/j.jhazmat.2022.128768. Epub 2022 Mar 24.
Heterogeneous catalytic ozonation (HCO) has been widely applied for the treatment of wastewater. In order to maintain the structural stability and surface catalytic activity of heterogeneous catalysts during the HCO treatment of electroless nickel plating effluent (ENPE), a MnFeO-C@AlO catalyst with a core-shell structure was synthesized. MnFeO-C@AlO was characterized and applied in the removal of total nickel (T) and organic contaminants from actual ENPE, using a coupled system of HCO combined with a magnetic dithiocarbamate chelating resin (MnFeO-C@AlO/O-MDCR). Results show that embedding AlO with C and MnFeO significantly increased the T removal efficiency (99.3%), enhanced the O-utilization efficiency and improved the generation of reactive oxygen species (ROS). The reaction rate (k = 0.7641 min) and O-utilization efficiency established for T removal (ΔT/ΔO =0.221) by the MnFeO-C@AlO/O-MDCR system, were 220% and 140% higher than the AlO/O-MDCR system, respectively. Catalytic mechanism analysis demonstrated that surface hydroxyl groups, oxygen vacancy, metals, the carbon surface and its functional groups, can all potentially serve as catalytic active sites, with O and •OH considered to the predominant ROS. Overall, these findings verify that the synthesized MnFeO-C@AlO catalyst possesses excellent catalytic capabilities and outstanding structural stability, making it suitable for practical application in the treatment of wastewater effluent.
多相催化臭氧氧化(HCO)已广泛应用于废水处理。为了在化学镀镍废水(ENPE)的 HCO 处理过程中保持多相催化剂的结构稳定性和表面催化活性,合成了具有核壳结构的 MnFeO-C@AlO 催化剂。对 MnFeO-C@AlO 进行了表征,并将其应用于实际 ENPE 中总镍(T)和有机污染物的去除,采用 HCO 与磁性二硫代氨基甲酸盐螯合树脂(MnFeO-C@AlO/O-MDCR)耦合系统。结果表明,嵌入 C 和 MnFeO 的 AlO 显著提高了 T 的去除效率(99.3%),提高了 O 的利用率并增强了活性氧物质(ROS)的生成。MnFeO-C@AlO/O-MDCR 系统中 T 去除的反应速率(k=0.7641 min)和 O 利用率(ΔT/ΔO=0.221)分别比 AlO/O-MDCR 系统高 220%和 140%。催化机理分析表明,表面羟基、氧空位、金属、碳表面及其官能团都可能作为催化活性位点,O 和•OH 被认为是主要的 ROS。总的来说,这些发现证明了合成的 MnFeO-C@AlO 催化剂具有优异的催化能力和出色的结构稳定性,使其适合于实际废水处理中的应用。