Uptake of iron (III)-ethylenediamine-N, N, N', N'-tetraacetic acid complex by phosphatidylcholine lipid film. Part II. Effect of film curvature.

Mixed micelles formed in a ternary-solute aqueous solution of NaOH, iron (III)-ethylenediamine-N, N, N', N'-tetraacetic acid complex (Fe-EDTA) and 1,2-diheptanoyl-sn-glycero-3-phosphatidyl choline (DHPC) were studied and compared with the mixed adsorbed film reported in Part I of this series to clarify the effect of the curvature of molecular assemblies on the interactions between their Fe-EDTA and DHPC constituents. The critical micelle concentrations (CMCs), surface tension at the CMC, and solution pH were measured as functions of the mole fractions of NaOH and DHPC. Rigorous thermodynamic equations were derived, in which the overall proton dissociation equilibria of Fe-EDTA and DHPC were taken into consideration, and applied to experimental data to obtain phase diagrams of micelle formation and the micelle-adsorbed film equilibrium.

Uptake of iron (III)-ethylenediamine-N,N,N',N'-tetraacetic acid complex by phosphatidylcholine lipid film: Part I. Effect of bulk pH.

We studied a ternary solutes aqueous solution of NaOH, iron (III)-ethylenediamine-N,N,N',N'-tetraacetic acid complex (Fe-edta), and 1,2-diheptanoyl-sn-glycero-3-phosphatidylcholine (DHPC)/air interface system to clarify the interactions between iron complexes and lipids with a phosphatidylcholine head group. The solution surface tension and pH were measured as functions of the total molality of NaOH, Fe-edta and DHPC, and the mole fractions of NaOH and DHPC. Rigorous thermodynamic equations were derived, in which the overall proton dissociation equilibria of Fe-edta and DHPC were taken into consideration, and applied to experimental data to obtain phase diagram of adsorption.

Adsorption and phase transition of alkanol and fluoroalkanol at electrified mercury/aqueous solution interface.

The adsorption behavior and the phase transition of alkanol and fluoroalkanol at the electrified mercury/aqueous solution interface were investigated by the interfacial tension measurements and the thermodynamic analysis. In the alkanol system, it is found that the phase transitions in low interfacial densities occur: the ones from the zero adsorption to the gaseous or the expanded state and the gaseous to the expanded state at the electrified interface depending on the electrostatic nature as well as the concentration in the bulk phase. These phase transitions were verified by the thermodynamic equations derived by the assumption of coexistence of two phases at the electrified interface.