Abstract

In this study, two reactants (ruthenium chloride and sodium borohydrate) were premicellized in two separate microemulsions and brought into contact through intermicellar exchange to conduct the reaction. As a result, ruthenium nanoparticles were formed. The overall reaction rate was governed by the intermicellar exchange rate. Particle size was controlled by varying surfactant concentration, water-to-surfactant molar ratio (ω), precursor (ruthenium chloride) concentration, and molar ratio of reducing agent-to-reagent (R). Dynamic light scattering and transmission electron microscopy were used to determine the size, size distribution, and structure of the synthesized ruthenium nanoparticles. The molar ratio ω was varied from 3 to 7; sizes of the particles were found to be in the range of 17.08–25.09 nm. The precursor (ruthenium chloride) concentration was varied in the range of 0.1–0.3 M; particle size was observed to decrease up to 0.2 M then increase due to particle agglomeration at higher precursor concentrations. Smaller nanoparticles were obtained at higher R values due to faster intramicellar nucleation and growth rate. Dispersion destabilization of colloidal ruthenium nanoparticles was detected by Turbiscan.

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