Ce to enhance photocatalytic performance by CuO/CeO2 of peroxymonosulfate activation for rapid degradation of tetracycline hydrochloride

被引:2
作者
Li, Z. L. [1 ]
Liu, X. R. [1 ]
Liu, Y. B. [2 ]
Li, S. Y. [1 ]
Yuan, S. Y. [1 ]
Zhang, Z. R. [1 ]
Qi, X. N. [1 ]
机构
[1] Ningxia Normal Univ, Coll Chem & Chem Engn, Guyuan 756000, Peoples R China
[2] Nanjing Polytech Inst, Nanjing 210000, Peoples R China
关键词
OXYGEN VACANCIES; CATALYTIC DEGRADATION; HETEROJUNCTION; NANOSTRUCTURES; NANOPARTICLES; NANOCOMPOSITES; MORPHOLOGY; MECHANISM; BIOCHAR; GROWTH;
D O I
10.1007/s10854-022-09775-5
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
CuO/CeO2 microsphere was viewed as an economical and environment-friendly heterogeneous photocatalyst, which was synthesized via a co-precipitation technique. The physicochemical properties of as-prepared samples were characterized by various methods. 20 mg/L of TC-HCl was degraded completely within 20 min at 1 mmol peroxymonosulfate (PMS) under UV-visible light. The scavenging experiments and electron paramagnetic resonance (EPR) technologies revealed that SO4 center dot -, O-2(center dot -) and center dot OH were involved as active species in the CuO/CeO2/PMS system, which were responsible for efficient decomposition of TC-HCl. Moreover, it was applied to treat raw water containing TC-HCl, all the removal efficiencies were more than 89% within 22 min. The possible photocatalytic degradation mechanism for the TC-HCl was investigated. CuO/CeO2 exhibited significant light trapping enhancement after Ce introduced, which lead to enhance the photocatalytic performance. Therefore, the CuO/CeO2 can be utilized as an economical photocatalyst to activate PMS and decompose TC-HCl in aqueous solution.
引用
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页数:13
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