共 79 条
Activation of persulfate by CO2-activated biochar for improved phenolic pollutant degradation: Performance and mechanism
被引:230
作者:
Sun, Chen
[1
]
Chen, Tong
[1
]
Huang, Qunxing
[1
]
Zhan, Mingxiu
[1
,2
]
Li, Xiaodong
[1
]
Yan, Jianhua
[1
]
机构:
[1] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China
[2] China Jiliang Univ, Coll Metrol & Measurement Engn, Hangzhou 310018, Zhejiang, Peoples R China
基金:
国家重点研发计划;
中国博士后科学基金;
关键词:
CO2-activated biochar;
Persulfate;
Phenol;
Singlet state oxygen;
Electrons transfer;
Non-radical mechanism;
ADVANCED OXIDATION PROCESSES;
WASTE-WATER TREATMENT;
BASIC PH CONDITIONS;
ORGANIC-COMPOUNDS;
POROUS CARBON;
PEROXYMONOSULFATE ACTIVATION;
ELECTROCHEMICAL ACTIVATION;
HETEROGENEOUS CATALYSIS;
NONRADICAL OXIDATION;
HEATED PERSULFATE;
D O I:
10.1016/j.cej.2019.122519
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Environment-friendly and low-cost catalysts are important for persulfate based advanced oxidation processes. In this study, we reported a CO2-activated biochar (AC) as a low-cost and efficient catalyst for persulfate (PS) activation and the degradation of phenol and chlorophenols. The AC950 showed the best catalytic performance for PS with an oxidant utility of 0.5 mol/mol oxidant/h/g with an activation energy of 15.86 kJ/mol owing to its large surface area, rich surface defects, and well-modified oxygen functional groups. In contrast to a radical-based mechanism, this novel biochar/persulfate system works through a non-radical mechanism that includes singlet state oxygen generation and an electron transfer reaction pathway. The major degradation intermediate of the phenolic pollutant was identified to be benzoquinone; moreover, amongst chlorophenols, the parachlorine substituent was the first to degrade. The durability of the catalyst was low, it was deactivated primarily because of the oxidation of the carbon surface, and thermal regeneration was determined to be efficient for its recovery. Furthermore, HCO3- and HPO4(2)(-) were found to considerably inhibit the performance of the catalytic oxidation system.
引用
收藏
页数:11
相关论文