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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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页数:11
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