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藻类碳催化剂促进过一硫酸盐活化氧化有机染料:实验与理论研究进展

Peroxymonosulfate activation by algal carbocatalyst for organic dye oxidation: Insights into experimental and theoretical.

机构信息

School of Environmental and Civil Engineering, Jiangnan University, Wuxi 214122, PR China.

School of Environmental and Civil Engineering, Jiangnan University, Wuxi 214122, PR China; Jiangsu Key Laboratory of Anaerobic Biotechnology, Wuxi 214122, PR China; Jiangsu Collaborative Innovation Center of Technology and Material of Water Treatment, Suzhou 215011, PR China.

出版信息

Sci Total Environ. 2022 Apr 10;816:151611. doi: 10.1016/j.scitotenv.2021.151611. Epub 2021 Nov 12.

DOI:10.1016/j.scitotenv.2021.151611
PMID:34774953
Abstract

Preparation of nitrogen-doped algal carbocatalyst (NC) for peroxymonosulfate (PMS) activation to oxidative degrade methylene blue (MB), and the mechanism of radical and nonradical pathway in N-C/PMS system are investigated. Firstly, a series of N-doped carbonaceous materials (NC) were prepared using nitrogen-rich Taihu blue algae biomass as precursor at different annealing temperatures. It was found that the NC prepared by annealing at 800 °C (N-C-8) showed an optimal MB degradation performance of over 99% after 60 min. Confirmed by electron paramagnetic resonance (EPR) analyses and radical quenching experiments, radical and nonradical pathway (O oxidation and electron-transfer) are both involved in MB degraded process. Moreover, both graphitic N derived from the intrinsic Taihu blue algae, and nitrogen vacancy evolved from nitrogen dopants decomposition exhibited high correlation with the MB removal rate in the N-C/PMS system. Finally, three possible degradation pathways of MB were proposed based on the Density Functional Theory (DFT) calculation and identified intermediates. Overall, this work provides a new insight into the intrinsic roles of nitrogen-dopants and nitrogen vacancies on the as-prepared carbocatalyst for PMS activation, and advances the understanding of the resource utilization of algal biomass.

摘要

制备氮掺杂藻基碳催化剂(NC)用于过一硫酸盐(PMS)活化以氧化降解亚甲基蓝(MB),并研究了 N-C/PMS 体系中自由基和非自由基途径的机制。首先,使用富氮太湖水生蓝藻生物质作为前体,在不同的退火温度下制备了一系列氮掺杂碳质材料(NC)。结果发现,在 800°C 下退火制备的 NC(N-C-8)在 60 min 后表现出超过 99%的最佳 MB 降解性能。通过电子顺磁共振(EPR)分析和自由基猝灭实验证实,MB 降解过程涉及自由基和非自由基途径(O 氧化和电子转移)。此外,源于太湖水生蓝藻固有石墨 N 和氮掺杂剂分解产生的氮空位都与 N-C/PMS 体系中 MB 去除率高度相关。最后,根据密度泛函理论(DFT)计算和鉴定的中间体,提出了 MB 的三种可能的降解途径。总的来说,这项工作为氮掺杂剂和氮空位在过一硫酸盐活化制备的碳催化剂中的固有作用提供了新的见解,并推进了对藻类生物质资源利用的理解。

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