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Ashina, C., Pugazhenthiran, N., Sathishkumar, P., Selvaraj, M., Assiri, M. A., Rajasekaran, C., et al. (2023). Ultra-small Ni@NiFe2O4/TiO2 magnetic nanocomposites activated peroxymonosulphate for solar light-driven photocatalytic mineralization of Simazine. J. Environ. Chem. Eng., 11(6), 111342.
Abstract: In the heterogeneous photocatalytic degradation of environmental contaminants the recovery, reuse of employed nanocatalyst was crucial and it is essentially required for the scale up applications. Besides, designing a magnetic material with heterojunction that can effectively oxidize the toxic organic contaminants to non-toxic substance under different reaction conditions including direct solar light irradiation remains a challenge. Considering the above facts, herein, we tailored heterojunction between the magnetic materials and non-magnetic materials with ultra-small Ni nanoparticles modified NiFe2O4/TiO2 nanostructures (Ni@NiFe2O4/TiO2 magnetic nanocomposites) through a simple sonochemical route. The Raman phonons at similar to 540 cm(-1) consistent to nickel metal nanoparticles and the spinel ferrites crystal structure confirmed the formation of Ni@NiFe2O4/TiO2 magnetic nanocomposites. The reduced optical bandgap of the resulting nanocomposites indicated the effective absorption of direct solar light irradiation when compared to the bare TiO2. Thus in-turn, enhanced the photocatalytic efficiency of simazine degradation in the presence of Ni@NiFe2O4/TiO2 magnetic nanocomposites (k= 11.0 x 10(-4) s(-1)) and augmented the activation of peroxymonosulphate (PMS) in the presence of Ni@NiFe2O4/TiO2 magnetic nanocomposites (k= 32.5 x 10(-4) s(-1)). Ni@NiFe2O4/TiO2 +PMS exhibited 3 folds enhanced efficiency in the presence of sunlight. The as-prepared NiFe2O4/TiO2 magnetic nanocatalysts were more stable and the efficiency of simazine oxidation was approximately same for the continuous five cycles at the optimized experimental conditions. The Ni@NiFe2O4/TiO2 magnetic nanocomposites preparation and the activation of PMS may promise the applications in an efficient wastewater treatment.
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Ortega-Martinez, E., Toledo-Alarcon, J., Fernandez, E., Campos, J. L., Oyarzun, R., Etchebehere, C., et al. (2024). A review of autotrophic denitrification for groundwater remediation: A special focus on bioelectrochemical reactors. J. Environ. Chem. Eng., 12(1), 111552.
Abstract: Groundwater is an important resource that can help in climate change adaptation. However, the pollution of these aquifers with nitrate is a widespread problem of growing concern. Biological denitrification using inorganic electron donors shows significant advantages in treating nitrate-polluted groundwater where organic matter presence is negligible. However, mass transfer limitations and secondary contamination seem to be the major hinderance to spread the use of these technologies. This could be solved by the use of bioelectrochemical systems (BES), which emerge as an attractive technology to solve these problems due to the reported low energy demand and high denitrification rates. However, technical and operational issues must be considered to replicate these results at full-scale. This review summarizes the biological basis of autotrophic denitrification and the key aspects of its application in bioelectrochemical systems. In addition, an estimation of the capital costs required for the implementation of a BES considering different population sizes and initial nitrate concentration in the ground-water is made.
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