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Kinetics and Mechanism of the Oxidation of Ammonia by Ferrate(VI) in Aqueous Solutions

  • Fengqin Wang
  • , Lin Li
  • , Hui-Mei Shan
  • , Xinru Li
  • , Sushan Feng
  • , Tai-Chu Lau*
  • , Yingying Liu*
  • , Qian Wang*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

Metal oxo complexes are potentially useful for the catalytic oxidation of ammonia to produce nitrite/nitrate or for the construction of ammonia fuel cell. In the work we have studied the kinetics and mechanisms of the oxidation of ammonia by ferrate(VI) (FeO42–), a well-defined metal oxo species. The kinetics was investigated over a pH range of 7.5 to 10, the rate-law is rate=k2[ferrate][ammonia]. k2 decrease with increasing pH, the results indicated that at pH 7.5 the reacting species are HFeO4– and NH4+, while at pH >9 the reacting species are FeO42– and NH3. At pH 7.5 the reaction occurs according to the following stoichiometry: 8HFeO4– + 3NH4+ + 3H2O →8Fe(OH)3 + 3NO3– + 2OH–. Nitrate is also formed as the predominantly product at higher pHs. Based on the experimental results and DFT calculations, the proposed mechanism involves an oxygen-atom transfer from ferrate(VI) to ammonia to produce hydroxylamine, which is then rapidly oxidized by excess ferrate to nitrate. © 2025 Wiley-VCH GmbH.
Original languageEnglish
Article numbere202400733
JournalEuropean Journal of Inorganic Chemistry
Volume28
Issue number6
Online published10 Jan 2025
DOIs
Publication statusPublished - 21 Feb 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Research Keywords

  • Ammonium oxidation
  • DFT
  • Ferrate
  • Nitrate
  • Oxygen-atom transfer

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