4.7 Article

Performance investigation of electrochemical assisted HClO/Fe2+ process for the treatment of landfill leachate

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 29, Issue 31, Pages 46875-46884

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-022-19174-2

Keywords

Advanced oxidation process; Active chlorine; Electrochemical Fenton-type process; Landfill leachate; COD; NH4+-N

Funding

  1. Fundamental Research Funds for the Central Universities, China [02190052020062]
  2. National Natural Science Foundation of China [52100073]

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This study demonstrates for the first time the feasibility of removing COD and NH4+-N from landfill leachate using an electrochemical assisted HClO/Fe2+ process. The performance of active chlorine generation at the anode was evaluated, and the coexistence of (OH)-O-center dot and (FeO2+)-O-IV in the system was confirmed. The influence of pH, Fe2+ concentration, and current density on COD and NH4+-N removal was investigated, and the reaction mechanism was proposed. The proposed process shows promise as an alternative for treating refractory landfill leachate.
The feasibility of removal of chemical oxygen demand (COD) and ammonia nitrogen (NH4+-N) from landfill leachate by an electrochemical assisted HClO/Fe2+ process is demonstrated for the first time. The performance of active chlorine generation at the anode was evaluated in Na2SO4/NaCl media, and a higher amount of active chlorine was produced at greater chloride concentration and higher current density. The probe experiments confirmed the coexistence of hydroxyl radical ((OH)-O-center dot) and Fe(IV)-oxo complex ((FeO2+)-O-IV) in the HClO/Fe2+ system. The influence of initial pH, Fe2+ concentration, and applied current density on COD and NH4+-N abatement was elaborately investigated. The optimum pH was found to be 3.0, and the proper increase in Fe2+ dosage and current density resulted in higher COD removal due to the accelerated accumulation of (OH)-O-center dot and (FeO2+)-O-IV in the bulk liquid phase, whereas, the NH4+-N oxidation was significantly affected by the applied current density because of the effective active chlorine generation at higher current but was nearly independent of Fe2+ concentration. The reaction mechanism of electrochemical assisted HClO/Fe2+ treatment of landfill leachate was finally proposed. The powerful (OH)-O-center dot and (FeO2+)-O-IV, in concomitance with active chlorine and M((OH)-O-center dot), were responsible for COD abatement, and active chlorine played a key role in NH4+-N oxidation. The proposed electrochemical assisted HClO/Fe2+ process is a promising alternative for the treatment of refractory landfill leachate.

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