Facile Solubilization of Organochalcogen Compounds in Mixed Micelle Formation of Binary and Ternary Cationic−Nonionic Surfactant Mixtures

2009 ◽  
Vol 113 (20) ◽  
pp. 7188-7193 ◽  
Author(s):  
S. K. Mehta ◽  
Savita Chaudhary ◽  
Rajeev Kumar ◽  
K. K. Bhasin
2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Olaseni Segun Esan ◽  
Medinat Olubunmi Osundiya ◽  
Christopher Olumuyiwa Aboluwoye ◽  
Owoyomi Olanrewaju ◽  
Jide Ige

Mixed-micelle formation in the binary mixtures of dodecyltrimethylammonium bromide (DTABr) and cetyltrimethylammonium bromide (CTABr) surfactants in water-ethanolamine mixed solvent systems has been studied by conductometric method in the temperature range of 298.1 to 313.1 K at 5 K intervals. It was observed that the presence of ethanolamine forced the formation of mixed micelle to lower total surfactant concentration than in water only. The synergistic interaction was quantitatively investigated using the theoretical models of Clint and Rubingh. The interaction parameter β12 was negative at all the mole fractions of DTABr in the surfactant mixtures indicating a strong synergistic interaction, with the presence of ethanolamine in the solvent system resulting in a more enhanced synergism in micelle formation than in water only. The free energy of micellization ΔGM values was more negative in water-ethanolamine mixed solvent system than in pure water indicating more spontaneity in mixed micelle formation in the presence of ethanolamine than in pure water.


1996 ◽  
Vol 13 (5) ◽  
pp. 377-395 ◽  
Author(s):  
Ajay K. Vanjara ◽  
Sharad G. Dixit

Mixed micelle formation between the anionic surfactant p-dodecyl benzene sulphonate and the non-ionic surfactants Brij-58, Brij-78 and Brij-99, having the same number of oxyethylene units but a varying number of hydrophobic groups, has been studied using surface tension and NMR spectroscopic measurements. Both hydrophobic–hydrophobic and hydrophilic–hydrophilic interactions play an important role in mixed micelle formation leading to greater non-ideality. The effect of mixed micelle interactions on the adsorption of these surfactants from their mixtures on rutile have been investigated using adsorption and zeta potential measurements. Adsorption above the CMC level is dictated by the relatively higher tendency of mixed micellization over mixed aggregation at the solid/liquid interface.


Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3288
Author(s):  
Ádám Juhász ◽  
László Seres ◽  
Norbert Varga ◽  
Ditta Ungor ◽  
Marek Wojnicki ◽  
...  

While numerous papers have been published according to the binary surfactant mixtures, only a few articles provide deeper information on the composition dependence of the micellization, and even less work attempts to apply the enhanced feature of the mixed micelles. The most important parameter of the self-assembled surfactants is the critical micelle concentration (cmc), which quantifies the tendency to associate, and provides the Gibbs energy of micellization. Several techniques are known for determining the cmc, but the isothermal titration calorimetry (ITC) can be used to measure both cmc and enthalpy change (ΔmicH) accompanying micelle formation. Outcomes of our calorimetric investigations were evaluated using a self-developed routine for handling ITC data and the thermodynamic parameters of mixed micelle formation were obtained from the nonlinear modelling of temperature- and composition- dependent enthalpograms. In the investigated temperature and micelle mole fractions interval, we observed some intervals where the cmc is lower than the ideal mixing model predicted value. These equimolar binary surfactant mixtures showed higher solubilization ability for poorly water-soluble model drugs than their individual compounds. Thus, the rapid and fairly accurate calorimetric analysis of mixed micelles can lead to the successful design of a nanoscale drug carrier.


1995 ◽  
Vol 67 (11) ◽  
pp. 1872-1880 ◽  
Author(s):  
Dolores. Sicilia ◽  
Soledad. Rubio ◽  
Dolores. Perez-Bendito

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Shuaijiang Jin ◽  
Roberto J. Brea ◽  
Andrew K. Rudd ◽  
Stuart P. Moon ◽  
Matthew R. Pratt ◽  
...  

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