Adsorption and degradation of tetracycline hydrochloride in aqueous solutions using activated carbon with Fe/Ag nanoparticles

被引:8
作者
Li, Wenbin [1 ]
Zhou, Zhijian [1 ]
Chen, Zhili [1 ]
Chen, Li [1 ]
Tang, Jin [1 ]
Zhang, Lizhao [1 ]
机构
[1] Guilin Univ Technol, Coll Environm Sci & Engn, Guilin 541004, Peoples R China
关键词
Nano zero-valent iron/nano silver; Activated carbon carriers; Tetracycline hydrochloride; Degradation mechanism; ZERO-VALENT IRON; REMOVAL; ANTIBIOTICS; KINETICS; WATER; CONTAMINANTS; REDUCTION; BEHAVIOR; FE/NI;
D O I
10.1016/j.mtcomm.2024.108504
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this study, a new adsorbent denoted as nAg/nZVI/AC was developed using activated carbon (AC) loaded with nanosized zero-valent iron (nZVI) and nanosilver (nAg). Then, the adsorption and degradation of tetracycline hydrochloride (TCH) in aqueous solutions using nAg/nZVI/AC was examined. At pH 3.8, the adsorbed amount of TCH on nAg/nZVI/AC was 191.18 mg/g, which is 78.95 mg/g higher than that adsorbed on the pristine AC support. The adsorption process could be explained adequately using the Freundlich (R2 = 0.9641) and pseudosecond-order kinetic models (R2 = 0.9967). Thermodynamic analyses revealed that TCH removal is a spontaneous chemisorption-dominated process. Free-radical-quenching experiments and electron paramagnetic resonance spectroscopic studies revealed that hydroxyl (& sdot;OH) and superoxide (& sdot;O2- ) radicals are the main species involved in the degradation of TCH. Finally, the intermediates generated during the degradation were examined using liquid chromatography-mass spectrometry, and possible deterioration pathways are proposed.
引用
收藏
页数:15
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