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EN
The density and surface tension of melts of the systems CaO-FeO-Fe2O3 MgO at the temperature 1623 K, CaO-FeO-Fe2O3-ZnO at 1573 K, and CaO-Fe2O3-Cu2O at 1573 K were determined using the maximum bubble pressure method. The molar volume, the excess molar volume, and the excess surface tension were calculated on the basis of the obtained data. From these properties information on the interactions of components and possible chemical reactions between them was obtained. Due to the absence of silica and the low concentration of other network-forming oxides, only isolated FeO45− tetrahedra and the CaO·FeO ionic pairs are formed in these basic melts, the donor of the oxygen atoms being either CaO, FeO, or both CaO+FeO oxides. Even the observed ternary interactions may be attributed to the formation of the anions FeO45− only.
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issue 3
471-480
EN
A simple theoretical model considering cell membrane mechanosensitivity can accurately describe published experimental data on membrane area creeping and recovery, and on osmotic expansion and rupture. The model to data fit reveals real values of membrane tension and elasticity modulus, and the parameters describing membrane organization and kinetics of mechanosensitive membrane traffic, including small solute transport, water permeability, endocytosis, exocytosis, and caveolae formation. This estimation allows for separation and quantitative analysis of the participation of different processes constituting the response of plasmalemma to short time-scale membrane load. The predicted properties of the model were verified for membrane stretching at different osmotic pressures. Finally, a simple hypothesis concerning stressed cell membrane breakdown is postulated.
Open Physics
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2005
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vol. 3
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issue 2
247-257
EN
The problem of size dependence of surface tension was investigated in view of a more general problem of the applicability of Gibbs’ thermodynamics to nanosized objects. For the first time, the effective surface tension (coinciding with the specific excess free energy for an equimolecular dividing surface) was calculated within a wide temperature range, from the melting temperature to the critical point, using the thermodynamic perturbation theory. Calculations were carried out for Lennard-Jones and metallic nanosized droplets. It was found that the effective surface tension decreases both, with temperature and particle size.
7
51%
EN
The problem of applicability of thermodynamics to small objects has been investigated. It is shown that the Gibbs surface phase method may be extended to nanoparticles if the effective surface tension (the specific excess free energy) is interpreted as a function of the particle radius.
Open Physics
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2003
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vol. 1
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issue 2
344-354
EN
Thermodynamic stability conditions for nanoparticles (resulting from non-negativity of the second variation of the free energy) have been analyzed for two cases: (i) a nonvolatile nanosized particle with the size-dependent surface tension; (ii) the limiting case of larger objects when the surface tension takes its macroscopic value. It has been shown that the mechanical stability of a nanoparticle, i.e. its stability relative to the volume fluctuations, is defined by an interplay between the excess (“surface”) free energy and the volumetric elastic energy. According to the results obtained, noble gas clusters and metal nanoparticles satisfy the mechanical stability condition. At the same time, water nanodrops, as well as nanoparticles presented by nonpolar organic molecules, correspond to the stability limit. Among the investigated systems, the stability condition is not carried out for n-Pentane clusters.
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