Photoassisted activation of persulfate by Cu2(OH)2CO3 for the degradation of tetracycline hydrochloride

IF 1 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Digest Journal of Nanomaterials and Biostructures Pub Date : 2024-03-01 DOI:10.15251/djnb.2024.191.309
S. J. Li, E. Pang, W. J. Zhao
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Abstract

Cu2(OH)2CO3 (cupric carbonate basic, CCB) is a common copper-based semiconductor compound that can absorb the visible light due to its suitable bandgap structure. Here, CCB was synthesized by a one-pot hydrothermal strategy. The catalyst exhibited excellent activation activity of persulfate (PS) supported by visible light irradiation and can degrade tetracycline hydrochloride (TCH) over a wide pH range from 3.0 to 10.0. Under the condition of 0.1 g/L catalyst and 2 mM PS, the removal rate of TCH (30 mg/L) reached 96% after 60 min of visible light irradiation. Coexisting anions (Cl- , HCO3 - , SO4 2- ) had little effect on the TCH degradation. The synergistic effects of CCB combined with PS and visible light were beneficial for the separation of photogenerated hole-electrons and the generation of more free radicals. Electron paramagnetic resonance (EPR) experiments and quenching experiments show that HO∙ and h+ are the predominant species in the catalytic reaction. Thus, this study proposes a promising approach using the CCB/PS/Vis system for wastewater remediation.
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光助 Cu2(OH)2CO3 活化过硫酸盐以降解盐酸四环素
Cu2(OH)2CO3(碱式碳酸铜,CCB)是一种常见的铜基半导体化合物,由于其合适的带隙结构,可以吸收可见光。本文采用一锅水热法合成了 CCB。该催化剂在可见光照射下对过硫酸盐(PS)具有良好的活化活性,可在 3.0 至 10.0 的宽 pH 值范围内降解盐酸四环素(TCH)。在 0.1 g/L 催化剂和 2 mM PS 的条件下,可见光照射 60 分钟后,TCH(30 mg/L)的去除率达到 96%。共存阴离子(Cl-、HCO3-、SO4 2-)对 TCH 降解的影响很小。CCB 与 PS 和可见光的协同作用有利于分离光生空穴电子和产生更多自由基。电子顺磁共振(EPR)实验和淬灭实验表明,HO∙和 h+ 是催化反应中的主要物种。因此,本研究提出了一种利用 CCB/PS/Vis 系统进行废水修复的可行方法。
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来源期刊
Digest Journal of Nanomaterials and Biostructures
Digest Journal of Nanomaterials and Biostructures 工程技术-材料科学:综合
CiteScore
1.50
自引率
22.20%
发文量
116
审稿时长
4.3 months
期刊介绍: Under the aegis of the Academy of Romanian Scientists Edited by: -Virtual Institute of Physics operated by Virtual Company of Physics.
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