Study on Reversible Solubilization by Adjusting Surfactant Properties.

Solubilization allows us to dissolve hydrophobic materials in water and to carry them to where they are needed. The purpose of this study is to control solubilization, especially the release of solubilized materials, via external stimulation. An amphoteric surfactant, dodecyldimethyl(3-sulfopropyl)ammonium hydroxide inner salt (SB-12), was employed, and a pH change was chosen as the external stimulus.

Effect of Hydrophobic Chains on Solubilization of Hydrocarbon and Fluorocarbon Surfactant Mixtures in Aqueous Solution.

We investigated the solubilization behavior of the hydrocarbon surfactant lithium dodecyl sulfate (LiDS) and the fluorocarbon surfactant lithium 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-1-octanesulfonate (LiFOS) in an aqueous solution to determine the controlled release mechanism of solubilizate. The LiDS system solubilized Sudan III, a hydrocarbon compound, whereas the LiFOS system did not, because of the immiscibility of the hydrocarbon and fluorocarbon compounds. The solubilization ability of the LiDS and LiFOS mixtures gradually decreased with increasing LiFOS bulk composition because the micelles mainly composed of LiDS transformed into micelles mainly composed of LiFOS.

Study on Colloid Vibration Current in Aqueous Solution of Binary Surfactant Mixtures: Effects of Counterions and Hydrophobic Chains.

In order to elucidate an electroacoustic phenomenon of mixed micelles in an aqueous solution, we measured the colloid vibration current (CVI) in aqueous solutions of binary surfactant mixtures. Based on the thermodynamic treatment of critical micelle concentration (cmc) values determined by conductivity measurements, it was expected that dodecyltrimethylammonium bromide (DTAB) and dodecyltrimethylammonium chloride (DTAC) molecules would mix ideally in the micelle. However, the micelle composition as evaluated from the CVI measurement, based on the linear dependence of the CVI value on the micelle composition, differed from the aforementioned ideality.

Effect of ionic surfactants on ion vibration current and colloid vibration current.

In order to clarify the effect of constituent ions on an electroacoustic phenomenon in an aqueous solution of ionic surfactant, we measured the total vibration current (TVI) as a function of the molarity of aqueous solution of several ionic surfactants at 298.15 K under atmospheric pressure. The different counterion caused the remarkable change in TVI, while the difference in alkyl chain length of surfactant ion hardly affected TVI.

Micelle formation effect on electroacoustics in an aqueous surfactant solution: colloid vibration current and ion vibration current.

We measured the ultrasonic vibration current of aqueous solution of dodecyltrimethylammonium bromide (DTAB) and dodecyltrimethylammonium chloride (DTAC) as a function of surfactant concentration at 298.15 K under atmospheric pressure. The dependence of vibration current on the surfactant concentration exhibited a break point around the critical micelle concentration (CMC) in the DTAB system, whereas no break point was observed in the DTAC system.

Impacts of papain and neuraminidase enzyme treatment on electrohydrodynamics and IgG-mediated agglutination of type A red blood cells.

The stability of native and enzyme-treated human red blood cells of type A (Rh D positive) against agglutination is investigated under conditions where it is mediated by immunoglobuline G (IgG) anti-D antibody binding. The propensity of cells to agglutinate is related to their interphasic (electrokinetic) properties. These properties significantly depend on the concentration of proteolytic papain enzyme and protease-free neuraminidase enzyme that the cells are exposed to.

Adsorption of surfactant ions and binding of their counterions at an air/water interface.

An expression for the surface tension of an aqueous mixed solution of surfactants and electrolyte ions in the presence of the common ions was derived from the Helmholtz free energy of an air/water surface. By applying the equation to experimental data for the surface tension, the adsorption constant of surfactant ions onto the air/water interface, the binding constant of counterions on the surfactants, and the surface potential and surface charge density of the interface were estimated. The adsorption constant and binding constant were dependent on the species of surfactant ion and counterion, respectively.

Study on the surface density of surface-active substances through total-reflection X-ray absorption fine structure measurement.

The total-reflection X-ray absorption fine structure (XAFS) method previously employed for the adsorption of dodecyltrimethylammonium bromide (DTAB) at the air/water interface was applied to that in the presence of NaBr. The surface concentration of the bromide ions Gamma(X)(B) of DTAB and NaBr was evaluated by using the Br K-edge absorption jump values of the total-reflection XAFS spectra and was compared to the corresponding value Gamma(H)(B) estimated from the dependence of surface tension on the bulk concentrations of DTAB m(1) and NaBr m(2). The Gamma(X)(B) values trace almost perfectly the Gamma(X)(B) versus m(1) curve up to a concentration near the critical micelle concentration (cmc) and deviate gradually above the concentration.

Effect of omega-hydrogenation on the adsorption of fluorononanols at the hexane/water interface: miscibility in the adsorbed film of fluorononanols.

The interfacial tension of the hexane solution of 1H,1H-perfluorononanol (FDFC9OH) and its omega-hydrogenated analogue, 1H,1H,9H-perfluorononanol (HDFC9OH), against water was measured as a function of the total molality and composition of the mixture at 298.15 K under atmospheric pressure. The existence of omega-dipole in HDFC9OH makes the interfacial density larger in the gaseous and expanded states and smaller in the condensed state compared to FDFC9OH.

Line tension and wetting behavior of an air/hexadecane/aqueous surfactant system.

The line tension of an air/hexadecane/aqueous solution of an dodecyltrimethylammonium bromide (DTAB) system was measured as a function of the molality of DTAB at 298.15 K by means of a newly constructed apparatus. It was estimated to be on the order of 10(-10)-10(-12) N, which is comparable to the theoretical estimation.

Selective determination of surface density of bromide ion through XAFS and its application to verification of a criterion of an ideal mixing of surfactant mixture.

The mole fraction of chloride ion of dodecyltrimethylammonium bromide (DTAB) and dodecyltrimethylammonium chloride (DTAC) mixture in the adsorbed film XHC was estimated not only by the thermodynamic analysis of the surface tension data but also by analyzing the Br K-edge jump of the XAFS spectrum under the total reflection condition (TRXAFS method). The phase diagrams of adsorption (PDA) at several surface tensions from the two methods were in good agreement. On the basis of the PDA obtained, it was clearly shown that the criterion of an ideal mixing for the DTAB-DTAC system is not given by the linear relation between the total molality of surfactant mixture m and XHC, m = m0B + (m0C - m0B)XHC, but by the one between m2 and XHC, m2 = (m0B)2 + [(m0C)2 - (m0B)2]XHC.

Aggregate formation in oil and adsorption at oil/water interface: thermodynamics and its application to the oleyl alcohol system.

The thermodynamic equations for examining aggregate formation in an oil phase and adsorption at the oil/water interface of a nonionic solute were derived. The total differentials of chemical potentials of species and the oil/water interfacial tension were expressed as functions of temperature, pressure, and the total concentration of solute in the oil phase after explicit consideration of aggregate formation. The partial derivatives of the chemical potentials and the interfacial tension with respect to the independent variables were found to provide the thermodynamic quantities of aggregate formation and adsorption from oil phase to the interface by introducing the concept of an ideally dilute associated solution.