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Chitosan Supports Boosting NiCo(2)O(4) for Catalyzed Urea Electrochemical Removal Application

Currently, wastewater containing high urea levels poses a significant risk to human health. Else, electrocatalytic methodologies have the potential to transform urea present in urea-rich wastewater into hydrogen, thereby contributing towards environmental conservation and facilitating the production...

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Detalles Bibliográficos
Autores principales: Alamro, Fowzia S., Hefnawy, Mahmoud A., Nafee, Sherif S., Al-Kadhi, Nada S., Pashameah, Rami Adel, Ahmed, Hoda A., Medany, Shymaa S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384518/
https://www.ncbi.nlm.nih.gov/pubmed/37514447
http://dx.doi.org/10.3390/polym15143058
Descripción
Sumario:Currently, wastewater containing high urea levels poses a significant risk to human health. Else, electrocatalytic methodologies have the potential to transform urea present in urea-rich wastewater into hydrogen, thereby contributing towards environmental conservation and facilitating the production of sustainable energy. The characterization of the NiCo(2)O(4)@chitosan catalyst was performed by various analytical techniques, including scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Furthermore, the activity of electrodes toward urea removal was investigated by several electrochemical techniques. As a function of current density, the performance of the modified NiCo(2)O(4)@chitosan surface was employed to remove urea using electrochemical oxidation. Consequently, the current density measurement was 43 mA cm(−2) in a solution of 1.0 M urea and 1.0 M KOH. Different kinetic characteristics were investigated, including charge transfer coefficient (α), Tafel slope (29 mV dec(−1)), diffusion coefficient (1.87 × 10(−5) cm(2) s(−1)), and surface coverage 4.29 × 10(−9) mol cm(−2). The electrode showed high stability whereas it lost 10.4% of its initial current after 5 h of urea oxidation.