Non-metal activated peroxydisulfate by straw biochar for tetracycline hydrochloride oxidative degradation: catalytic activity and mechanism

被引:10
作者
Chen, Chen [1 ]
Sun, Hao [1 ]
Zhang, Shengyu [1 ,2 ]
Su, Xiaosi [1 ,2 ]
机构
[1] Jilin Univ, Key Lab Groundwater Resources & Environm, Minist Educ, Changchun 130021, Peoples R China
[2] Jilin Univ, Inst Water Resources & Environm, Changchun 130026, Peoples R China
基金
中国国家自然科学基金;
关键词
Biochar; Tetracycline; Peroxydisulfate; Reactive oxygen species; Degradation; PERSISTENT FREE-RADICALS; WASTE-WATER TREATMENT; PYROLYSIS TEMPERATURE; PERSULFATE; CARBON; SLUDGE; ADSORPTION; PEROXYMONOSULFATE; SULFAMETHOXAZOLE; POLLUTANTS;
D O I
10.1007/s11356-023-25761-8
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, stalk biochar (BC) was prepared by a high-temperature pyrolysis process and used as a non-metallic catalyst to activate peroxydisulfate (PDS) to degrade tetracycline hydrochloride (TCH). Various characterization results showed that BC had a hollow tubular structure, irregular folds, and important active sites such as oxygen-containing functional groups. Under the optimal reaction conditions, the degradation rate of TCH reached 98.1% within 120 min. In addition, the degradation performance was satisfactory and similar under acidic and near neutral pH, and higher temperature promoted the degradation of TCH. The SO4 center dot(-), center dot OH, and O-1(2) generated by PDS activation were reactive oxygen species (ROS), which degraded TCH through free radical/non-radical synergistic pathways. Quenching experiments proved that the generated SO4 center dot(-) and center dot OH might be the dominant reactive oxygen species (ROS) during the oxidative reaction. The research results will provide a theoretical basis for the application of PDS activated by non-metallic catalysts in the remediation of tetracycline antibiotics pollution.
引用
收藏
页码:50815 / 50828
页数:14
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