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使用双金属CoO/ZnO氧化物高效降解罗丹明B:过一硫酸盐的超快和持久活化

Efficiently Degrading RhB Using Bimetallic CoO/ZnO Oxides: Ultra-Fast and Persistent Activation of Permonosulfate.

作者信息

Sun Bai, Liu Rui, Zhao Fengshou, He Shengnan, Wang Yun, Wang Xiangxiang, Huang Hao, Yi Mingjian, Zhu Shuguang

机构信息

Engineering Research Center of Building Energy Efficiency Control and Evaluation, Ministry of Education, College of Environment and Energy Engineering, Anhui Jianzhu University, Hefei 230601, China.

Environmental Materials and Pollution Control Laboratory, Hefei Institute of Physical Science, Chinese Academy of Sciences, Hefei 230031, China.

出版信息

Molecules. 2025 May 21;30(10):2237. doi: 10.3390/molecules30102237.

Abstract

To address the issues of poor Co regeneration and limited interfacial electron transfer in heterogeneous catalytic systems, this study proposes the synthesis of highly efficient and stable CoO/ZnO composites through the pyrolysis-oxidation reaction of Co/Zn MOFs for the degradation of rhodamine B (RhB) using activated peroxymonosulfate (PMS). The results confirmed that the catalyst exhibited a high electron transfer capacity, and the synergistic effect between the bimetals enhanced the reversible redox cycle of Co/Co. Under optimal conditions, complete removal of RhB was achieved in just 6 min using the CoO/ZnO composite, which demonstrated excellent stability after five cycles. Furthermore, the catalyst exhibited a high degradation efficiency in real water samples with a total organic carbon (TOC) removal rate of approximately 65% after 60 min. The electrochemical measurements, identification of active species, and X-ray photoelectron spectroscopy (XPS) analysis revealed that non-radicals (O and direct charge transfer) played a major role in the degradation of RhB. Finally, the potential mechanisms and degradation pathways for RhB degradation using this catalyst were systematically investigated. This study opens new avenues for the development of efficient and stable PMS catalysts, and provides insights into the preparation of other emerging metal oxides.

摘要

为了解决多相催化体系中钴再生性能差和界面电子转移受限的问题,本研究提出通过钴/锌金属有机框架材料的热解氧化反应合成高效稳定的CoO/ZnO复合材料,用于活化过一硫酸盐(PMS)降解罗丹明B(RhB)。结果证实,该催化剂具有较高的电子转移能力,双金属之间的协同作用增强了Co/Co的可逆氧化还原循环。在最佳条件下,使用CoO/ZnO复合材料仅需6分钟就能完全去除RhB,并且在五个循环后仍表现出优异的稳定性。此外,该催化剂在实际水样中也表现出较高的降解效率,60分钟后总有机碳(TOC)去除率约为65%。电化学测量、活性物种鉴定和X射线光电子能谱(XPS)分析表明,非自由基(O和直接电荷转移)在RhB的降解中起主要作用。最后,系统地研究了使用该催化剂降解RhB的潜在机制和降解途径。本研究为开发高效稳定的PMS催化剂开辟了新途径,并为制备其他新型金属氧化物提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/922d/12114238/c5b3141a0aed/molecules-30-02237-g001.jpg

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