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Assessing the potential of biochar derived from sewage sludge for photoelectrode fabrication: methods, mechanisms, and conclusions
被引:4
|作者:
Peng, Chuangxin
[1
]
Huang, Jing
[2
]
Ruan, Min
[3
]
Peng, Haihao
[1
]
Jia, Meiying
[4
]
Tong, Jing
[1
]
Xiong, Weiping
[1
]
Yang, Zhaohui
[1
]
机构:
[1] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Peoples R China
[2] Hunan Acad Forestry, State Key Lab Utilizat Woody Oil Resource, Changsha 410004, Peoples R China
[3] Changsha Univ Sci & Technol, Sch Energy & Power Engn, Changsha 410076, Peoples R China
[4] Cent South Univ Forestry Technol, Coll Environm Sci & Engn, Changsha 410004, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CATALYTIC DEGRADATION;
ACTIVE-SITES;
CARBON;
ADSORBENT;
ENERGY;
WATER;
D O I:
10.1039/d3ta03147k
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Previous studies often utilized metal catalysts in the preparation of photoelectrodes. However, this research marks the first instance of utilizing biochar as a catalyst in such a preparation. The biochar catalytic layer was synthesized by loading sewage sludge-derived biochar onto nickel foam using the sol-gel method. The performance of the photoelectrode was evaluated using tetracycline (TC) as a probe. The photoelectrode BCPE-800, prepared using biochar derived at 800 & DEG;C, achieved 98.52% TC degradation within 60 min, with a reaction rate constant of 0.0635 min(-1). It also exhibited excellent stability and recyclability, maintaining 90% removal efficiency after six cycles. Quenching experiments and EPR spectroscopy showed that h(+) acted as the primary active species, while OH and O-1(2) also contributed to the TC degradation. Based on the intermediates identified by LC-MS, the study proposed two degradation pathways. The research effectively recycled sewage sludge and offered cost-effective possibilities for photoelectrocatalytic technology, highlighting its practical applications.
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页码:15256 / 15268
页数:13
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