Abstract

The incorporation of an extracting agent di-(2-ethylhexyl)phosphoric acid (D2EHPA) into non-ionic surfactant, Triton X-100 (TX-100) micelles was investigated by monitoring the microstructural changes using light scattering (LS) and small angle neutron scattering (SANS) techniques. Dynamic light scattering (DLS) studies indicate a gradual increase in the apparent diffusion coefficient (Da) of the micelles upon addition of D2EHPA, suggesting the incorporation of D2EHPA molecules into TX-100 micelles. Quantitative analysis of the SANS data for D2EHPA containing micelles indicates that the effective surface charge on the micelles increases with increasing concentration of D2EHPA, while the dimensions of the micelles remain almost same. Thus, the observed increase in Da of the micelles is attributed to the changes in the intermicellar interactions. The increase in repulsive interaction with addition of D2EHPA is also evident from an increase in the cloud point of the micellar solutions. The microstructural and cloud point changes occurred in D2EHPA containing micelles in the presence of an inorganic salt, sodium chloride (NaCl) further support the inclusion of D2EHPA molecules into TX-100 micelles. The binding of uranyl ions (UO22+) to TX-100–D2EHPA mixed micelles was ensured by monitoring a decrease in the intermicellar repulsion upon addition of uranyl nitrate hexahydrate and a subsequent decrease in the cloud point of the micelles. A red-shift in the absorption peaks of uranyl nitrate hexahydrate in the presence of TX-100–D2EHPA mixed micelles also confirms the binding of UO22+ to mixed micelles. The quantitative estimation of UO22+ bound to TX-100–D2EHPA mixed micelles was carried by cloud point extraction (CPE) method followed by spectrophotometric determination.

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