Pt-based graphene quantum dots for water dissociation.

It is widely recognized that Pt nanostructures exhibit favorable catalytic properties for several important technological reactions. Furthermore, selecting an appropriate support has the potential to enhance the catalytic activity of these materials. In this study, we investigate Pt nanoparticles deposited on quantum dots using quantum chemical calculations. We explore the utilization of low-dimensional carbonaceous support by employing graphene quantum dots (GQDs), which offer abundant active sites, such as edges, and diverse conformations. This provides excellent tuning possibilities for both chemical and physical properties. Our goal is to gather information on the alterations in electronic properties, charge redistribution and reactivity of platinum particles on GQD, also analyzing their potential role as catalysts in the water dissociation reaction. Based on thermodynamic and kinetic considerations, our calculations suggest that a Pt3nanoparticle adsorbed on the edge of the GQD exhibits favorable energetics, leading to a promising catalytic material.

Treatment of Cyanide-Free Wastewater from Brass Electrodeposition with EDTA by Electrodialysis: Evaluation of Underlimiting and Overlimiting Operations.

Growing environmental concerns have led to the development of cleaner processes, such as the substitution of cyanide in electroplating industries and changes in the treatment of wastewaters. Hence, we evaluated the treatment of cyanide­free wastewater from the brass electroplating industry with EDTA as a complexing agent by electrodialysis, aimed at recovering water and concentrated solutions for reuse. The electrodialysis tests were performed in underlimiting and overlimiting conditions. The results suggested that intense water dissociation occurred at the cathodic side of the commercial anion­exchange membrane (HDX) during the overlimiting test. Consequently, the pH reduction at this membrane may have led to the reaction of protons with complexes of EDTA-metals and insoluble species. This allowed the migration of free Cu2+ and Zn2+ to the cation-exchange membrane as a result of the intense electric field and electroconvection. These overlimiting phenomena accounted for the improvement of the percent extraction and percent concentration, since in the electrodialysis stack employed herein, the concentrate compartments of cationic and anionic species were connected to the same reservoir. Chronopotentiometric studies showed that electroconvective vortices minimized fouling/scaling at both membranes. The electrodialysis in the overlimiting condition seemed to be more advantageous due to water dissociation and electroconvection.