过硫酸盐
催化作用
降级(电信)
电化学
双金属片
化学
化学工程
水处理
电子转移
碳纤维
氧化还原
材料科学
无机化学
复合数
光化学
电极
有机化学
废物管理
复合材料
电信
计算机科学
工程类
物理化学
作者
Bin Yao,Yuange Yu,Wancheng Zhu,Jian Yang,Yaoyu Zhou,Dionysios D. Dionysiou
标识
DOI:10.1016/j.cej.2023.146769
摘要
The booming demand for modern medicine has led to the widespread occurrence of antibiotics in aquatic environments. The co-activation of persulfate (PS) by electrochemical and catalytic processes has now drawn increasing interests for the treatment of refractory contaminants in water. Herein, N-doped porous carbon decorated with Fe/Ni bimetallic composite catalyst (FeNi-NC) was prepared with Fe-doped Ni-MOFs as a precursor. The composite catalyst was evaluated for it performance to catalyze PS in the presence of an electric field for the destruction of tetracycline (TC). Thanks to the synergistic effect between the electrochemical and Fe1Ni5-NC-600 catalytic processes to activate PS, the E-Fe1Ni5-NC-600 system exhibited a satisfactory performance for TC degradation, attaining a 91.94 % removal within 90 min. Electric field accelerated the redox cycles of Fe0/Fe2+/Fe3+ and Ni0/Ni2+/Ni3+ to realize the sustainable catalytic activation of PS to form reactive species (OH, SO4−, and 1O2) for enhanced TC degradation. Competition kinetics studies suggested OH was the dominant reactive species, and electron-transfer process also contributed to TC removal. Moreover, the E-Fe1Ni5-NC-600/PS system exhibited a low energy consumption (0.34 kWh/m3-log), wide effectiveness in the elimination of on different organic pollutants, and good applicability for real water treatment. This study provided new insights into the application of PS-based advanced oxidation process for the high-performance treatment of antibiotic-containing wastewater.
科研通智能强力驱动
Strongly Powered by AbleSci AI