{"title":"Oxygen-vacancy-rich N-doped NiFe2O4 activates peroxymonosulfate for efficient water purification","authors":"Donglei Fu, Zhengxiong Zhao, Pengwei Yan, Zhonglin Chen, Jinxiang Zuo","doi":"10.1016/j.seppur.2025.134061","DOIUrl":null,"url":null,"abstract":"An efficient catalyst with abundant oxygen vacancies (OVs) was obtained via nitrogen (N) doping NiFe<sub>2</sub>O<sub>4</sub> for peroxymonosulfate (PMS) activation to achieve durable water purification. The N-NiFe<sub>2</sub>O<sub>4</sub> activated process enhanced the formation of SO<sub>4</sub><sup><img alt=\"radical dot\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/rad.gif\" style=\"vertical-align:middle\"/>−</sup> and ·OH, thus endowing the system with high decontamination performance compared to pristine NiFe<sub>2</sub>O<sub>4</sub>. The influence of complex aquatic matrices on the N-NiFe<sub>2</sub>O<sub>4</sub>/PMS system towards 2,4-dichlorophenoxyacetic acid (2,4-D) removal was investigated in detail. The systematic evaluation revealed that the 5.0 % N-doped NiFe<sub>2</sub>O<sub>4</sub>/PMS system demonstrated optimal catalytic activity, achieving an 86.9 % removal efficiency of 2,4-D within 15 min. Radical quenching experiments identified SO<sub>4</sub><sup><img alt=\"radical dot\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/rad.gif\" style=\"vertical-align:middle\"/>−</sup> and ·OH were predominantly responsible for 2,4-D degradation. According to the in situ tests and Density functional theory (DFT) calculation, the constructed OVs on N-NiFe<sub>2</sub>O<sub>4</sub> greatly promoted the adsorption of PMS, and next served as reactive sites for electron transfer via the Fe<sup>3+</sup> or Ni<sup>2+</sup> sites, which further activated PMS for the formation of SO<sub>4</sub><sup><img alt=\"radical dot\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/rad.gif\" style=\"vertical-align:middle\"/>−</sup>. In short, this work gives an effective strategy to prepare high-performance catalysts for durable water purification system construction.","PeriodicalId":427,"journal":{"name":"Separation and Purification Technology","volume":"12 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-06-19","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://doi.org/10.1016/j.seppur.2025.134061","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
An efficient catalyst with abundant oxygen vacancies (OVs) was obtained via nitrogen (N) doping NiFe2O4 for peroxymonosulfate (PMS) activation to achieve durable water purification. The N-NiFe2O4 activated process enhanced the formation of SO4− and ·OH, thus endowing the system with high decontamination performance compared to pristine NiFe2O4. The influence of complex aquatic matrices on the N-NiFe2O4/PMS system towards 2,4-dichlorophenoxyacetic acid (2,4-D) removal was investigated in detail. The systematic evaluation revealed that the 5.0 % N-doped NiFe2O4/PMS system demonstrated optimal catalytic activity, achieving an 86.9 % removal efficiency of 2,4-D within 15 min. Radical quenching experiments identified SO4− and ·OH were predominantly responsible for 2,4-D degradation. According to the in situ tests and Density functional theory (DFT) calculation, the constructed OVs on N-NiFe2O4 greatly promoted the adsorption of PMS, and next served as reactive sites for electron transfer via the Fe3+ or Ni2+ sites, which further activated PMS for the formation of SO4−. In short, this work gives an effective strategy to prepare high-performance catalysts for durable water purification system construction.
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.