RESUMO
The Leidenfrost effect is a phenomenon in which a liquid, poured onto a glowing surface significantly hotter than the liquid's boiling point, produces a layer of vapor that prevents the liquid from rapid evaporation. Rather than making physical contact, a drop of water levitates above the surface. The temperature above which the phenomenon occurs is called the Leidenfrost temperature. The reason for the existence of the Leidenfrost temperature, which is much higher than the boiling point of the liquid, is not fully understood and predicted. For water we prove that the Leidenfrost temperature corresponds to a bifurcation in the solutions of equations describing evaporation of a nonequilibrium liquid-vapor interface. For water, the theoretical values of obtained Leidenfrost temperature, and that of the liquid-vapor interface which is smaller than the boiling point of liquid, fit the experimental results found in the literature.
RESUMO
The aim of the paper is the study of fluid mixtures in nanotubes by the methods of continuum mechanics. The model starts from a statistical distribution in mean-field molecular theory and uses a density expansion of Taylor series. We get a continuous expression of the volume free energy with density's spatial derivatives limited at the second order. The nanotubes can be filled with liquid or vapor according to the chemical characteristics of the walls and of liquid or vapor mixture bulks. An example of a two-fluid mixture constituted of water and ethanol inside carbon nanotubes at 20^{∘}C is considered. When diameters are small enough, nanotubes are filled with a liquid mixture whatever are the liquid or vapor mixture bulks. The carbon wall influences the ratio of the fluid components in favor of ethanol. The fluid mixture flows across nanotubes can be much more important than classical ones and if the external bulk is vapor, then the flow can be several hundred thousand times larger than Poiseuille flow.
RESUMO
Thanks to an expansion with respect to densities of energy, mass and entropy, we discuss the concept of thermocapillary fluid for inhomogeneous fluids. The non-convex state law valid for homogeneous fluids is modified by adding terms taking account of the gradients of these densities. This seems more realistic than Cahn and Hilliard's model which uses a density expansion in mass-density gradient only. Indeed, through liquid-vapour interfaces, realistic potentials in molecular theories show that entropy density and temperature do not vary with the mass density as it would do in bulk phases. In this paper, we prove using a rescaling process near the critical point, that liquid-vapour interfaces behave essentially in the same way as in Cahn and Hilliard's model.
RESUMO
We can propound a thermo-mechanical understanding of the ascent of sap to the top of tall trees thanks to a comparison between experiments associated with the cohesion-tension theory and the disjoining pressure concept for liquid thin-films. When a segment of xylem is tight-filled with crude sap, the liquid pressure can be negative although the pressure in embolized vessels remains positive. Examples are given that illustrate how embolized vessels can be refilled and why the ascent of sap is possible even in the tallest trees avoiding the problem due to cavitation. However, the maximum height of trees is limited by the stability domain of liquid thin-films.
Assuntos
Árvores/anatomia & histologia , Árvores/fisiologia , Água , Ar , Movimento (Física) , Pressão , Vapor , TermodinâmicaRESUMO
We present a classical approach to a mixture of compressible fluids when each constituent has its own temperature. The introduction of an average temperature together with the entropy principle dictates the classical Fick law for diffusion and also novel constitutive equations associated with the difference of temperatures between the components. The constitutive equations fit with results recently obtained through a Maxwellian iteration procedure in extended thermodynamics theory of multitemperature mixtures. The differences of temperatures between the constituents imply the existence of a dynamical pressure even if the fluids have a zero bulk viscosity. The nonequilibrium dynamical pressure can be measured and may be convenient in several physical situations, such as, for example, in cosmological circumstances where--as many authors assert--a dynamical pressure played a major role in the evolution of the early universe.