{"title":"MOF-derived CuCo carbon microspheres assembled with nitrogen-doped carbon nanotubes as PMS activator for the efficient degradation of p-nitrophenol","authors":"Qingqing Shi, Yaqi Hou, Qiting Zhu, Yongmei Hao","doi":"10.1016/j.seppur.2024.129107","DOIUrl":null,"url":null,"abstract":"<div><p>Due to the complex structure of metal–carbon-based catalysts derived from metal-organic frameworks (MOFs), it is difficult to clarify the active sites and catalytic mechanisms. Constructing of structure–activity relationship is conducive for identifying active center, but there is still a gap in the bimetal-carbon-based catalysts/PMS systems. Here, we report a highly efficient and stable CuCo bimetal-nitrogen doped carbon catalyst (CuCo@C-N) for the activation of PMS for efficient degradation of PNP. By manipulating the catalyst structure, establishing the structure–activity relationship and combining with DFT calculation, the non-metallic active centers were determined, including defects, C=O and graphite N. Co was the only metal active center, and the presence of Cu accelerated the redox cycle of the system. The degradation of PNP was dependent on electron transfer and ROS activation. The metal active center was used to generate sulfate radicals (SO<sub>4</sub><sup>•−</sup>), and the non-metal active sites accelerated electron transfer and non-radical pathways to generate <sup>1</sup>O<sub>2</sub>.</p></div>","PeriodicalId":427,"journal":{"name":"Separation and Purification Technology","volume":"354 ","pages":"Article 129107"},"PeriodicalIF":9.0000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Separation and Purification Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1383586624028466","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Due to the complex structure of metal–carbon-based catalysts derived from metal-organic frameworks (MOFs), it is difficult to clarify the active sites and catalytic mechanisms. Constructing of structure–activity relationship is conducive for identifying active center, but there is still a gap in the bimetal-carbon-based catalysts/PMS systems. Here, we report a highly efficient and stable CuCo bimetal-nitrogen doped carbon catalyst (CuCo@C-N) for the activation of PMS for efficient degradation of PNP. By manipulating the catalyst structure, establishing the structure–activity relationship and combining with DFT calculation, the non-metallic active centers were determined, including defects, C=O and graphite N. Co was the only metal active center, and the presence of Cu accelerated the redox cycle of the system. The degradation of PNP was dependent on electron transfer and ROS activation. The metal active center was used to generate sulfate radicals (SO4•−), and the non-metal active sites accelerated electron transfer and non-radical pathways to generate 1O2.
期刊介绍:
Separation and Purification Technology is a premier journal committed to sharing innovative methods for separation and purification in chemical and environmental engineering, encompassing both homogeneous solutions and heterogeneous mixtures. Our scope includes the separation and/or purification of liquids, vapors, and gases, as well as carbon capture and separation techniques. However, it's important to note that methods solely intended for analytical purposes are not within the scope of the journal. Additionally, disciplines such as soil science, polymer science, and metallurgy fall outside the purview of Separation and Purification Technology. Join us in advancing the field of separation and purification methods for sustainable solutions in chemical and environmental engineering.