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WATER RESEARCH · 2025 · IF 12.4

Manipulating Electrochemical Phosphate Recovery from Acidic Wastewater for Synthesizing LiFePO4/C Cathode Material

Bingnan Song,Wei Chen,Ying Pu,Weiquan Li,Zhengshuo Zhan,Haisheng Fang,Yang Lei

Phosphorus (P) recovery from wastewater offers a sustainable solution for mitigating pollution and securing resources for applications like lithium-ion batteries, where ferric phosphate is a valuable precursor. This study evaluates iron electrolysis for P removal and recovery from acidic wastewater with high phosphate concentrations and medium Ca²⁺ levels. The results suggested that effective P removal and high-purity iron phosphate production can be achieved by varying initial pH, current density, and oxidation conditions. Importantly, slow Fe release rates (0.02–0.04 mmol L⁻¹ min⁻¹) favored ferric phosphate formation (71%–77% removal), while faster rates (0.16–0.46 mmol L⁻¹ min⁻¹) predominantly produced vivianite (∼65% removal). In addition, air flush can enhance dissolved oxygen flux, achieving 89% P removal under rapid Fe release but with mixed products. H₂O₂ addition improved in situ Fe(II) oxidation, achieving 92% P removal and purer ferric phosphate. Compared to chemical precipitation, which required pH adjustment and suffered from Ca co-precipitation, iron electrolysis produced purer ferric phosphate directly, without pH pre-adjustment. The recovered ferric phosphate showed excellent potential as a precursor for high-performance LiFePO₄/C cathode material. These findings position iron electrolysis as a promising approach for sustainable P recovery and resource valorization from wastewater.

研究领域: 环境科学 · 电化学 · 材料科学
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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY · 2015 ·Vol. 91 ·期 4 ·938-947 · IF 2.349

Iron electrolysis-assisted peroxymonosulfate chemical oxidation for the remediation of chlorophenol-contaminated groundwater

Nuo Yang,Jiaxin Cui,Lieyu Zhang,Wei Xiao,Akram N Alshawabkeh,Xuhui Mao

BACKGROUND Electrolysis with an iron anode is a novel way to provide ferrous activators for chemical oxidation. The objective of this study is to evaluate the performance of peroxymonosulfate (PMS) for chlorophenol destruction when compared with H 2 O 2 and persulfate (PS), and to see whether the electrolysis mode facilitates the buildup of conditions that favor the activation of PMS and removal of chlorophenols. RESULTS Ferrous species can effectively activate the PMS over a wide pH range. In comparison with H 2 O 2 and PS, PMS is less sensitive to the solution's pH and possesses stronger oxidation capability at alkaline pHs. The optimal molar ratio of PMS to Fe(II) activator is 1:1 for the destruction of 2,4-dichlorophenol (2,4-DCP). The column experiments show that an acidic zone developed downstream from the anode is favorable to maintain ferrous ions and subsequent activation of PMS. The reactivity of the PMS can be manipulated by varying the electrical currents, and the process demonstrates effectiveness for treating organic contaminants. 2,4-DCP contaminated groundwater shows decreased biotoxicity after the chemical oxidation process without considering the residual PMS. CONCLUSIONS Iron electrolysis-assisted peroxymonosulfate chemical oxidation can effectively treat the 2,4-dichlorophenol and mixtures of organic contaminants. This process can be engineered as an in situ chemical oxidation method for groundwater remediation. © 2015 Society of Chemical Industry

CAS / MDL: 1415-93-6 70693-62-8
研究领域: 环境科学 · 化学工程
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