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碳酸钙激活 HO-HCO 降解污染物。

Activation of HO-HCO by CaCoO for pollutant degradation.

机构信息

School of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan, 430200, P. R. China.

Hubei Key Laboratory of Biomass Fibers and Eco-Dyeing & Finishing, Wuhan Textile University, Wuhan, 430200, P. R. China.

出版信息

Environ Sci Pollut Res Int. 2024 Jul;31(35):48450-48459. doi: 10.1007/s11356-024-34398-0. Epub 2024 Jul 20.

DOI:10.1007/s11356-024-34398-0
PMID:39031318
Abstract

The bicarbonate-activated hydrogen peroxide (BAP) system is widely studied for organic pollutant degradation in wastewater treatment. CaCoO, a heterogeneous catalyst containing multivalent cobalt including Co(II) and Co(III), was herein investigated as a BAP activator, and Acid Orange 7 (AO7) was used as a model pollutant. CaCoO exhibited good activation performance. The degradation rate and the initial rate constant of the CaCoO-activated BAP system were 5.4 and 11.2 times as high as the BAP system, respectively. The removal rate of AO7 reached 90.9% in 30 min under optimal conditions (AO7 20 mg/L, CaCoO 0.2 g/L, HO 1 mM, NaHCO 5 mM, pH 8.5, 25℃). The CaCoO catalyst exhibited good stability and recyclability, retaining 85% of AO7 removal rate in the fifth run. Compared to the BAP system, a lower dosage of HO was required and a higher initial concentration of pollutants allowed for effective degradation in the CaCoO-BAP system. X-ray photoelectron spectroscopy was used to analyze the catalytic mechanism. The analysis showed that the good catalytic performance of CaCoO attributes to its high proportion of oxygen vacancies and Co(III) species, and the presence of Ca. The active species O, •OH, and O are responsible for the degradation, as indicated by the quenching experiments. The degradation mechanism of AO7 was speculated based on UV-Vis spectral analysis and the identification of degradation intermediates. The azo form, naphthalene and benzoic rings in the AO7 structure are destroyed in the decomposition. This research provides a feasible approach to designing effective and reusable BAP activators for pollutant degradation in wastewater treatment.

摘要

过碳酸盐激活过氧化氢(BAP)体系在废水处理中广泛用于有机污染物降解。CaCoO 是一种含有多价钴(包括 Co(II) 和 Co(III))的多相催化剂,本文将其作为 BAP 激活剂进行研究,以酸性橙 7(AO7)作为模型污染物。CaCoO 表现出良好的激活性能。与 BAP 体系相比,CaCoO 激活的 BAP 体系的降解速率和初始速率常数分别提高了 5.4 倍和 11.2 倍。在最佳条件下(AO7 20mg/L、CaCoO 0.2g/L、HO 1mM、NaHCO 5mM、pH 8.5、25℃),30min 内 AO7 的去除率达到 90.9%。CaCoO 催化剂表现出良好的稳定性和可回收性,在第五次运行中仍保留 85%的 AO7 去除率。与 BAP 体系相比,CaCoO-BAP 体系需要更少的 HO 用量和更高的污染物初始浓度,即可实现有效降解。X 射线光电子能谱用于分析催化机制。分析表明,CaCoO 的高比例氧空位和 Co(III)物种以及 Ca 的存在是其良好催化性能的原因。淬灭实验表明,活性物质 O、•OH 和 O 是导致降解的原因。根据 UV-Vis 光谱分析和降解中间体的鉴定,推测了 AO7 的降解机制。AO7 结构中的偶氮形式、萘和苯甲酸环在分解过程中被破坏。本研究为设计用于废水处理中污染物降解的有效且可重复使用的 BAP 激活剂提供了一种可行的方法。

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