Electrophoretic mobility of SiO nanoparticles in a n-hexadecane-chloroform mixture depending on AOT concentration and chloroform content was determined. It was shown that an increase in chloroform content and a decrease in AOT concentration cause a growth in electrophoretic mobility. The use of the values of Debye lengths (characteristic thickness) of the diffuse part of the electric double layer (EDL) that were determined previously allowed us to calculate the electrokinetic potential and to evaluate the stability of organosols.
View Article and Find Full Text PDFThe structure and conductivity of AOT (sodium bis(2-ethylhexyl) sulfosuccinate) solutions (2.5 × 10 -2.5 × 10 M) in n-hexadecane-chloroform mixture at the chloroform concentration from 50 to 100 vol% were studied.
View Article and Find Full Text PDFThe electrophoretic mobility of Ag and Au nanoparticles in n-hexadecane-chloroform mixtures was studied as a function of the chloroform content (from 0 to 100 vol%). The nanoparticles were stabilized by sodium bis-(2-ethylhexyl)sulfosuccinate (AOT, Aerosol OT) with a concentration of 2.5 × 10-4 mol L-1.
View Article and Find Full Text PDFIn this work, we tried to combine the advantages of microemulsion and emulsion synthesis to obtain stable concentrated organosols of Ag nanoparticles, promising liquid-phase materials. Starting reagents were successively introduced into a micellar solution of sodium bis-(2-ethylhexyl)sulfosuccinate (AOT) in n-decane in the dynamic reverse emulsion mode. During the contact of the phases, Ag passes into micelles and Na passes into emulsion microdroplets through the cation exchange AOTNa + AgNO = AOTAg + NaNO.
View Article and Find Full Text PDFStable organosols of TiO nanoparticles were prepared by hydrolysis of titanium tetraisopropoxide (TTIP) in microemulsions of sodium bis(2-ethylhexyl)sulfoxynate (АОТ) in n-decane with increasing the content of aqueous pseudophase from 0.15 to 0.85 vol.
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