Waste coconut shell-derived carbon monolith as an efficient binder-free cathode for electrochemical advanced oxidation treatment of endocrine-disrupting compounds.

J Environ Manage

School of Environmental Science and Engineering, Indian Institute of Technology Kharagpur, Kharagpur, 721302, India; Department of Civil Engineering, Indian Institute of Technology Kharagpur, Kharagpur, 721302, India. Electronic address:

Published: December 2023

AI Article Synopsis

  • Discharge of endocrine disruptors like methylparaben into water bodies harms aquatic life, and electrochemical methods like electrochemical oxidation (EO) and electro-Fenton (EF) are effective for removing such contaminants.
  • Researchers used carbonized coconut shell (CCS) as an affordable cathode in these processes, achieving nearly complete removal of methylparaben within 60 minutes for EO and 45 minutes for EF at specific conditions.
  • The CCS-based system outperformed commercial alternatives in contaminant removal and demonstrated effective treatment of real sewage, maintaining high efficiency over multiple cycles while supporting eco-friendly degradation pathways.

Article Abstract

Discharge of endocrine-disrupting compounds such as methylparaben (MePa) into natural water bodies deteriorates the aquatic ecosystem. In this regard, electrochemical oxidation (EO) and electro-Fenton (EF) processes are acknowledged as effective methods to eliminate biorecalcitrant compounds from different wastewater matrices. In these systems, the HO-producing ability of carbon-based cathodes is put to advantage for producing homogenous hydroxyl radicals by simulating Fenton's reaction, which dramatically augments the contaminant removal efficiency. However, commercial carbon based cathodes are not economically affordable, especially for voluminous treatment. Hence in the present work, waste-derived carbonised coconut shell (CCS) monolith was employed as a cathode in EO and EF treatment of MePa. Almost the entire MePa with initial concentration of 10 mg/L was removed in 60 min by EO and 45 min by EF process at neutral pH, applied current density of 7.5 mA/cm, NaCl concentration of 1.0 g/L and 10 mg/L of FeO dosing. The MePa removal efficiency of the CCS cathode-fitted system after 60 min was better than the commercial graphite plate and Ti-based mixed metal oxide employing system due to higher HO electrosynthesis (HO = 9.0 ± 0.6 mg/L after 60 min). Moreover, the same setup was used for treating 10 mg/L of MePa-spiked real sewage and demonstrated MePa and total organic carbon removal efficiency of 80.16 ± 2.31% and 37.42 ± 3.50%, respectively, in 45 min. Further, the CCS-mediated EF treatment achieved >90% removal of MePa for eight continuous batch cycles and recorded a current density drop of just 0.23% per cycle. The degradation pathway and toxicity assessment of the intermediates using the Ecological Structure Activity Relationships (ECOSAR) tool supported the eco-friendliness of the current treatment scheme.

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http://dx.doi.org/10.1016/j.jenvman.2023.119328DOI Listing

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