Search

A comprehensive study has been carried out to evaluate the extraction of heavy metals mixture (Co2+, Cr3+, Cu2+, Ni2+) from aqueous media by Winsor II non-ionic microemulsion, containing polyoxyethylene (4) lauryl ether as non-ionic surfactant and butyl acetate as organic phase. The extraction mechanism is based on the formation of thiocyanate complexes of metals and their transfer from aqueous to microemulsion phase, either towards the interfacial film of surfactant (Co2+) or into the core of micelles (Cr3+, Cu2+, Ni2+). The value of the distribution coefficient for Co2+ was higher than for the other studied metals and its extraction efficiency was not dependent on the working conditions, showing a maximum value (99.99%) in all cases. By using successive extractions, chromium, nickel and copper ions that remained in the aqueous phase after first extraction were transported into the microemulsion phase, leading to an increase in the extraction efficiency up to 99.99% for chromium and copper, and 85% for nickel. Based on pH influence, a selective extraction of Co2+ and Cr3+ can be achieved, since the cobalt ions were completely extracted into the microemulsion phase at pH = 1, and the chromium ions still remained in the aqueous phase. Keywords: Nonionic microemulsion, Thiocyanate complexes of heavy metals, Simultaneous heavy metals extraction, Microinterfacial effect, Synergism

A class of fluorescent Au@SiO2 and SiO2@Au core–shell fluorescent nanoparticles has been synthesized using microemulsion assisted sol–gel method coupled with photoreduction reaction as an easy, rapid and versatile “one-pot” procedure. In the case of Au@SiO2-RhB (gold nanoparticles core coated with silica-Rhodamine B shell) different silica shell sizes were obtained ranging from 3 to 116 nm, while for RhB-SiO2@Au (Rhodamine B-silica core coated with gold nanoparticles shell) the size of gold shell falls within 3–38 nm interval. The synthesized core–shell nanoparticles have been characterized by a variety of techniques including Dynamic Light Scattering (DLS), High-Resolution Transmission Electron Microscopy (HR-TEM) coupled with Energy-Dispersive X-ray spectroscopy (EDX), Scanning Electron Microscopy (SEM), X-ray Diffractometry (XRD) and UV–VIS–NIR spectroscopy to confirm the size, shape, stability and topographic structure of the both core–shell nanostructures. The fluorescence enhancement of Rhodamine B (RhB) dye in the presence of gold nanoparticles (AuNPs) was demonstrated for the core–shell nanostructures synthesized in the present study, for different silica or gold shells. These interesting fluorescent core–shell nanoparticles provide ideal candidates for a variety of applications in materials science, biology, catalysis and optical fields.

The interactions of two ionic dyes, Crystal Violet and Methyl Orange, with different charged surfactants and also with a nonionic surfactant were investigated using surface tension measurements and visible spectroscopy in pre-micellar and post-micellar regions. It was found that for the water dominant phase systems the dye was localized between the polar heads, at the exterior of the direct micelle shells for all the systems. For the oil dominant phase systems, in case of the same charged dye/surfactant couples, the dye was localized in the micelle shell between the hydrocarbon chain of the surfactant nearby the hydrophilic head groups while for nonionic surfactant and oppositely charged dye/surfactant, localization of dye was between the oxyethylenic head groups towards the interior of the micelle core. Mixed aggregates of the dye and surfactant (below the critical micellar concentration of cationic surfactant), dye-surfactant ion pair and surfactant-micelles were present. The values of equilibrium constants (for TX-114/MO and TX-114/CV systems were 0.97 and 0.98, respectively), partition coefficients between the micellar and bulk water phases and standard free energy (for the nonionic systems were −12.59 kJ/mol for MO and −10.97 kJ/mol for CV) were calculated for all the studied systems. The partition processes were exothermic and occurred spontaneously.