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Tin Oxide Nanoparticles via Solar Vapor Deposition for Hexavalent Chromium Remediation

[Image: see text] Tin oxide nanoparticles optimized to capture low concentrations of hexavalent chromium from water were developed through a facile, scalable, and low-cost one-step solar vapor deposition methodology. Considering the preservation of high electron donation capacity as the key to suppo...

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Detalles Bibliográficos
Autores principales: Simeonidis, Konstantinos, Kalaitzidou, Kyriaki, Asimakidou, Theopoula, Martinez-Boubeta, Carlos, Makridis, Antonios, Haeussler, Anita, Vourlias, Georgios, Balcells, Lluis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502794/
https://www.ncbi.nlm.nih.gov/pubmed/37719329
http://dx.doi.org/10.1021/acsanm.3c01567
Descripción
Sumario:[Image: see text] Tin oxide nanoparticles optimized to capture low concentrations of hexavalent chromium from water were developed through a facile, scalable, and low-cost one-step solar vapor deposition methodology. Considering the preservation of high electron donation capacity as the key to support the reduction of mobile Cr(VI) into insoluble forms, the growth of SnO nanoparticles was favored by the co-evaporation of SnO(2) with Fe powders at various mass ratios. Characterization techniques indicated that the percentage and the stability of SnO is proportional to the Fe content in the target with a requirement of at least 50% wt to inhibit the formation of a passive SnO(2) surface layer. The produced particles were evaluated regarding their efficiency to capture Cr(VI) under conditions similar to water treatment for drinking purposes (pH 7). It was revealed that passivation-free SnO nanoparticles deliver significant improvement in the adsorption capacity corresponding to the residual concentration of 25 μg/L, reaching a value of 1.74 mg/g for the sample prepared with 50% wt Fe in the target. The increase of water acidity was found responsible for the activation of more reduction sites on the particle surface, as reflected through the elevation of efficiency by more than 20% at pH 6.