Salt assistant bimetallic sludge-derived porous carbon for efficient peroxymonosulfate activation

被引:1
|
作者
Zhao, Wenyu [1 ]
Yao, Yiyuan [1 ]
Wang, Pengfei [2 ]
Zhao, Xiaoyu [1 ]
Fan, Lulu [2 ]
Liu, Chuquan [1 ]
Chen, Zhiwen [1 ]
Xiao, Chengming [1 ]
Qi, Junwen [1 ]
Zhou, Yujun [1 ]
Zhu, Zhigao [1 ]
Yang, Yue [1 ]
Li, Jiansheng [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Jiangsu Key Lab Chem Pollut Control & Resources Re, Nanjing 210094, Peoples R China
[2] Shanxi North Xingan Chem Ind Co Ltd, Taiyuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Sludge-derived porous carbon; Peroxymonosulfate; Bimetallic synergy; Molten salt assistant; Radical pathway; BISPHENOL-A; DEGRADATION; OXIDATION; MECHANISM;
D O I
10.1016/j.seppur.2024.127811
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The development of cost-effective, environmentally benign, and high-performance peroxymonosulfate (PMS) activation towards wastewater treatment is still considered a challenge. In this work, the sludge-derived porous carbon loaded with bimetal oxides (DSC-FeMn) was fabricated by molten salt assistant strategy using the combination of zinc chloride, metal ions and Fe containing sludge. The obtained DSC-FeMn exhibited high catalytic activity for nearly 100 % 4-chlorophenol (4-CP) removal within 30 min with the k of 0.304 min(-1), which was 1.07 and 11.94 times that of the single Fe and Mn-sludge-derived carbon (DSC-Fe, DSC-Mn), respectively. Quenching experiments, electron paramagnetic resonance tests (EPR), X-ray photoelectron spectroscopy (XPS), H-2-temperature programmed reduction (H-2-TPR) and electrochemical experiments proved that the radical pathway, dominated by (OH)-O-center dot and SO4 center dot-, led to the excellent degradation performance of DSC-FeMn, which was attributed to the redox cycling between Fe and Mn. This study provides a new idea for sludge resource utilization, and it deepens the understanding of the mechanism of PMS activation by the synergistic interaction between bimetal.
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收藏
页数:11
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