{"title":"Self-regenerable zeolite Beta(35) for efficient adsorption and photocatalytic degradation of PFOA under simulated solar irradiation","authors":"Xiaoyu Li, Xuejing Xiao, Shengnan Zhang, Xiaolei Teng, Zunyao Wang, Ruijuan Qu","doi":"10.1016/j.watres.2025.124645","DOIUrl":null,"url":null,"abstract":"<div><div>Perfluorooctanoic acid (PFOA), a priority emerging pollutant, necessitates efficient and green removal methods. While adsorption is cost-effective under mild conditions, the adsorbent treatment often causes additional costs and limits its applicability. This study employs a BEA-topology zeolite (Beta(35)) as a bifunctional adsorbent and photocatalyst for PFOA removal. Beta(35) at a dosage of 0.25 g/L achieved 90.7 % adsorption of 20 mg/L PFOA within 1 h, with adsorption capacities reaching 80 mg/g. Under natural sunlight irradiation, Beta(35) demonstrated 85.2 % degradation efficiency and 63.1 % defluorination efficiency for PFOA within 24 h. Additionally, the feasibility of treating trace PFOA-contaminated water was confirmed, where 2 g of Beta(35) effectively enriched and degraded 4 L of simulated groundwater containing 50 μg/L PFOA, achieving a degradation efficiency of 94.1 % within 48 h. Theoretical calculations and spectral analyses confirmed that PFOA adsorbs onto the acidic sites of Beta(35) through bidentate/bridging coordination, reducing the C<img>C bond dissociation energy at the carboxyl end to facilitate degradation. Besides, the complexation of Beta(35) and PFOA improved the photocatalytic performance of Beta(35), facilitating the formation of <em>h</em><sup>+</sup> and ROS (•OH and •O<sub>2</sub><sup>−</sup>). Beta(35) remove aqueous PFOA via initial adsorption followed by photocatalytic degradation for self-regeneration, offering a sustainable and cost-effective solution for PFAS remediation.</div></div>","PeriodicalId":443,"journal":{"name":"Water Research","volume":"288 ","pages":"Article 124645"},"PeriodicalIF":12.4000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Water Research","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0043135425015489","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Perfluorooctanoic acid (PFOA), a priority emerging pollutant, necessitates efficient and green removal methods. While adsorption is cost-effective under mild conditions, the adsorbent treatment often causes additional costs and limits its applicability. This study employs a BEA-topology zeolite (Beta(35)) as a bifunctional adsorbent and photocatalyst for PFOA removal. Beta(35) at a dosage of 0.25 g/L achieved 90.7 % adsorption of 20 mg/L PFOA within 1 h, with adsorption capacities reaching 80 mg/g. Under natural sunlight irradiation, Beta(35) demonstrated 85.2 % degradation efficiency and 63.1 % defluorination efficiency for PFOA within 24 h. Additionally, the feasibility of treating trace PFOA-contaminated water was confirmed, where 2 g of Beta(35) effectively enriched and degraded 4 L of simulated groundwater containing 50 μg/L PFOA, achieving a degradation efficiency of 94.1 % within 48 h. Theoretical calculations and spectral analyses confirmed that PFOA adsorbs onto the acidic sites of Beta(35) through bidentate/bridging coordination, reducing the CC bond dissociation energy at the carboxyl end to facilitate degradation. Besides, the complexation of Beta(35) and PFOA improved the photocatalytic performance of Beta(35), facilitating the formation of h+ and ROS (•OH and •O2−). Beta(35) remove aqueous PFOA via initial adsorption followed by photocatalytic degradation for self-regeneration, offering a sustainable and cost-effective solution for PFAS remediation.
期刊介绍:
Water Research, along with its open access companion journal Water Research X, serves as a platform for publishing original research papers covering various aspects of the science and technology related to the anthropogenic water cycle, water quality, and its management worldwide. The audience targeted by the journal comprises biologists, chemical engineers, chemists, civil engineers, environmental engineers, limnologists, and microbiologists. The scope of the journal include:
•Treatment processes for water and wastewaters (municipal, agricultural, industrial, and on-site treatment), including resource recovery and residuals management;
•Urban hydrology including sewer systems, stormwater management, and green infrastructure;
•Drinking water treatment and distribution;
•Potable and non-potable water reuse;
•Sanitation, public health, and risk assessment;
•Anaerobic digestion, solid and hazardous waste management, including source characterization and the effects and control of leachates and gaseous emissions;
•Contaminants (chemical, microbial, anthropogenic particles such as nanoparticles or microplastics) and related water quality sensing, monitoring, fate, and assessment;
•Anthropogenic impacts on inland, tidal, coastal and urban waters, focusing on surface and ground waters, and point and non-point sources of pollution;
•Environmental restoration, linked to surface water, groundwater and groundwater remediation;
•Analysis of the interfaces between sediments and water, and between water and atmosphere, focusing specifically on anthropogenic impacts;
•Mathematical modelling, systems analysis, machine learning, and beneficial use of big data related to the anthropogenic water cycle;
•Socio-economic, policy, and regulations studies.