Degradation of 29 per- and poly-fluoroalkyl substances (PFAS) in water using fenton-assisted electrochemical oxidation process

IF 9 1区 工程技术 Q1 ENGINEERING, CHEMICAL Separation and Purification Technology Pub Date : 2025-02-02 DOI:10.1016/j.seppur.2025.131908
Huynh Do Hieu Nhu , Dao Van Tri , Tran Le Luu , Jana Trippel , Martin Wagner
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Abstract

Per-polyfluoroalkyl compounds (PFAS) are of widespread concern because they persist in water and resist conventional treatment processes, which may pose risks to human health and the environment. Therefore, this study for the first time focused on investigating the effectiveness of the fenton-assisted electrochemical oxidation process combined with a Pt cathode and two anodes (Ti/BDD and Ti/IrO2) in treating 29 PFAS compounds (divided into 8 groups: PFCAs, PFOSA, Linear and branched FOSAA, PFSAs, FTSA, Gen X, NaDONA and F-53B) in a simulated wastewater model based on the surface water content evaluated and quantified by liquid chromatography-tandem mass spectrometry (LC/MS-MS). Experimental results showed that the operating parameters that directly affect the treatment process were optimized, with the Ti/BDD anode demonstrating superior degradation efficiency under optimal operating conditions: [NaCl] 2 g/L, [Fe3O4] 0.5 mM, pH 2.5–3, applied current density 5 mA/cm2, stirring speed 200 rpm, electrolysis time 120 min removed 86.1–100 % PFAS per eight groups in water with an energy consumption of 9.0 kWh/m3. Comparatively, optimal operating conditions for the Ti/IrO2 anode were higher than Ti/BDD: [NaCl] 2 g/L, [Fe3O4] 1 mM, applied current density 15 mA/cm2, pH 3, stirring speed 200 rpm, electrolysis time 180 min, removing 54.5–98.1 % PFAS per eight groups with an energy consumption of 40.5 kWh/m3, respectively. Hydroxyl radicals (OH) generated during the process effectively degraded both long- and short-chain at 29 PFAS compounds, and the long-chain PFCAs and PFSAs groups, along with linear and branched PFAA isomers, were found to be more stable in degradation than the other groups. The hydrolysis mechanism is the proposed pathway for removing typical PFBS and intermediate compounds. This study suggested fenton-assisted electrochemical oxidation process with the Ti/BDD anode as a feasible method to reduce PFAS pollution in surface water, providing a sustainable and effective alternative to conventional treatment methods.

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fenton辅助电化学氧化法降解水中29种全氟和多氟烷基物质(PFAS
全多氟烷基化合物(PFAS)在水中持续存在,并抵抗常规处理工艺,可能对人类健康和环境构成风险,因此受到广泛关注。因此,本研究首次在模拟废水模型中,通过液相色谱-串联质谱(LC/MS-MS)对地表水含量进行评估和定量,研究了fenton辅助电化学氧化工艺处理29种PFAS化合物(分为PFCAs、PFOSA、线性和支链FOSAA、PFSAs、FTSA、Gen X、 NaDONA和F-53B 8组)的有效性。实验结果表明,在[NaCl] 2 g/L, [Fe3O4] 0.5 mM, pH 2.5-3,施加电流密度5 mA/cm2,搅拌速度200 rpm,电解时间120 min下,Ti/BDD阳极表现出优异的降解效率,每8组水中PFAS去除率为86.1-100 %,能耗为9.0 kWh/m3。相比之下,Ti/IrO2阳极的最佳操作条件高于Ti/BDD: [NaCl] 2 g/L, [Fe3O4] 1 mM,施加电流密度15 mA/cm2, pH 3,搅拌速度200 rpm,电解时间180 min,每8组去除54.5-98.1 %的PFAS,能耗分别为40.5 kWh/m3。在此过程中产生的羟基自由基(OH•)可以有效降解29种PFAS化合物的长链和短链,并且发现长链PFCAs和PFSAs基团以及线性和支链PFAA异构体的降解比其他基团更稳定。水解机制是提出的去除典型PFBS和中间化合物的途径。本研究表明,fenton-assisted electrochemical oxidation process with Ti/BDD阳极是一种减少地表水PFAS污染的可行方法,为传统的处理方法提供了一种可持续、有效的替代方法。
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来源期刊
Separation and Purification Technology
Separation and Purification Technology 工程技术-工程:化工
CiteScore
14.00
自引率
12.80%
发文量
2347
审稿时长
43 days
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.
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