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Comparative Study of the Effect of Doping ZnTiO with Rare Earths (La and Ce) on the Adsorption and Photodegradation of Cyanide in Aqueous Systems. | LitMetric

Comparative Study of the Effect of Doping ZnTiO with Rare Earths (La and Ce) on the Adsorption and Photodegradation of Cyanide in Aqueous Systems.

Int J Mol Sci

Ingeniería Química, Facultad de Ciencias Exactas y Naturales, Universidad Técnica Particular de Loja, San Cayetano Alto, Loja 1101608, Ecuador.

Published: February 2023

Cyanide is a highly toxic compound that can pose serious health problems to both humans and aquatic organisms. Therefore, the present comparative study focuses on the removal of total cyanide from aqueous solutions by photocatalytic adsorption and degradation methods using ZnTiO (ZTO), La/ZnTiO (La/ZTO), and Ce/ZnTiO (Ce/ZTO). The nanoparticles were synthesized by the sol-gel method and characterized by X-ray powder diffractometry (XRD), Scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDS), Diffuse reflectance spectroscopy (DRS), and Specific surface area (SSA). The adsorption equilibrium data were fitted to the Langmuir and Freundlich isotherm models. Adsorption kinetics were also evaluated using the pseudo-first-order and pseudo-second-order models and the intraparticle diffusion model. Likewise, the photodegradation of cyanide under simulated sunlight was investigated and the reusability of the synthesized nanoparticles for cyanide removal in aqueous systems was determined. The results demonstrated the effectiveness of doping with lanthanum (La) and cerium (Ce) to improve the adsorbent and photocatalytic properties of ZTO. In general, La/ZTO showed the maximum percentage of total cyanide removal (99.0%) followed by Ce/ZTO (97.0%) and ZTO (93.6%). Finally, based on the evidence of this study, a mechanism for the removal of total cyanide from aqueous solutions using the synthesized nanoparticles was proposed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9960395PMC
http://dx.doi.org/10.3390/ijms24043780DOI Listing

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