scholarly journals Extended Larché–Cahn framework for reactive Cahn–Hilliard multicomponent systems

Author(s):  
Santiago P. Clavijo ◽  
Luis Espath ◽  
Victor M. Calo

AbstractAt high temperature and pressure, solid diffusion and chemical reactions between rock minerals lead to phase transformations. Chemical transport during uphill diffusion causes phase separation, that is, spinodal decomposition. Thus, to describe the coarsening kinetics of the exsolution microstructure, we derive a thermodynamically consistent continuum theory for the multicomponent Cahn–Hilliard equations while accounting for multiple chemical reactions and neglecting deformations. Our approach considers multiple balances of microforces augmented by multiple component content balance equations within an extended Larché–Cahn framework. As for the Larché–Cahn framework, we incorporate into the theory the Larché–Cahn derivatives with respect to the phase fields and their gradients. We also explain the implications of the resulting constrained gradients of the phase fields in the form of the gradient energy coefficients. Moreover, we derive a configurational balance that includes all the associated configurational fields in agreement with the Larché–Cahn framework. We study phase separation in a three-component system whose microstructural evolution depends upon the reaction–diffusion interactions and to analyze the underlying configurational fields. This simulation portrays the interleaving between the reaction and diffusion processes and how the configurational tractions drive the motion of interfaces.

Author(s):  
H.H. Rotermund

Chemical reactions at a surface will in most cases show a measurable influence on the work function of the clean surface. This change of the work function δφ can be used to image the local distributions of the investigated reaction,.if one of the reacting partners is adsorbed at the surface in form of islands of sufficient size (Δ>0.2μm). These can than be visualized via a photoemission electron microscope (PEEM). Changes of φ as low as 2 meV give already a change in the total intensity of a PEEM picture. To achieve reasonable contrast for an image several 10 meV of δφ are needed. Dynamic processes as surface diffusion of CO or O on single crystal surfaces as well as reaction / diffusion fronts have been observed in real time and space.


2021 ◽  
Author(s):  
Jesús Ildefonso Díaz ◽  
David Gómez-Castro ◽  
Tatiana A. Shaposhnikova

Entropy ◽  
2018 ◽  
Vol 20 (10) ◽  
pp. 802 ◽  
Author(s):  
Sergey Serdyukov

In this work, we consider extended irreversible thermodynamics in assuming that the entropy density is a function of both common thermodynamic variables and their higher-order time derivatives. An expression for entropy production, and the linear phenomenological equations describing diffusion and chemical reactions, are found in the context of this approach. Solutions of the sets of linear equations with respect to fluxes and their higher-order time derivatives allow the coefficients of diffusion and reaction rate constants to be established as functions of size of the nanosystems in which these reactions occur. The Maxwell-Cattaneo and Jeffreys constitutive equations, as well as the higher-order constitutive equations, which describe the processes in reaction-diffusion systems, are obtained.


2005 ◽  
Vol 19 (01n03) ◽  
pp. 299-302 ◽  
Author(s):  
M. YU ◽  
H. Q. LIN

In this paper, we study phase separation in the two-dimensional single-band Hubbard model with the unrestricted Hartree-Fock(UHF) method and the restricted Hartree-Fock (RHF) method. We perform the calculation for square lattices and rectangle lattices. It is observed that the stripe phase exists and it depends on three aspects: geometry of the lattice, Coulomb interaction U and band filling n. To gain more physical insights, we consider the Hubbard model with spin dependent hoppings: t↑ and t↓, and study the effect of varying [Formula: see text] on the phase separation.


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