Energetic solutions to rate-independent processes are usually constructed via time-incremental minimization problems. In this work we show that all energetic solutions can be approximated by incremental problems if we allow approximate minimizers, where the error in minimization has to be of the order of the time step. Moreover, we study sequences of problems where the energy functionals have a Gamma limit.
This note addresses a three-dimensional model for isothermal stress-induced transformation in shape-memory polycrystalline materials. We treat the problem within the framework of the energetic formulation of rate-independent processes and investigate existence and continuous dependence issues at both the constitutive relation and quasi-static evolution level. Moreover, we focus on time and space approximation as well as on regularization and parameter asymptotics.
This paper deals with error estimates for space-time
discretizations of 3D model for isothermal stress-induced
transformations in shape-memory materials. After recalling
existence and uniqueness results, a fully-discrete approximation is presented and an explicit space-time
convergence rate of order is derived.
We consider systems of reaction-diffusion equations as gradient systems with respect to an entropy functional and a dissipation metric given in terms of a so-called Onsager operator, which is a sum of a diffusion part of Wasserstein type and a reaction part. We provide methods for establishing geodesic $\lambda$-convexity of the entropy functional by purely differential methods, thus circumventing arguments from mass transportation. Finally, several examples, including a drift-diffusion system, provide a survey on the applicability of the theory.
A general abstract approximation scheme for rate-independent processes in the
energetic formulation is proposed and its convergence is proved under various
rather mild data qualifications. The abstract theory is illustrated on several
examples: plasticity with isotropic hardening, damage, debonding,
magnetostriction, and two models of martensitic transformation in
shape-memory alloys.
This paper analyzes a model for phase
transformation in shape-memory alloys
induced by temperature changes and by
mechanical loading. We assume that the temperature is prescribed and
formulate the problem within the framework
of the energetic theory of
rate-independent processes. Existence and uniqueness results are proved.
This paper deals with error estimates for space-time discretizations in the context of evolutionary variational inequalities of rate-independent type. After introducing a general abstract evolution problem, we address a fully-discrete approximation and provide a priori error estimates. The application of the abstract theory to a semilinear case is detailed. In particular, we provide explicit space-time convergence rates for the isothermal Souza-Auricchio model for shape-memory alloys.
We derive thermodynamically consistent models of reaction-diffusion equations
coupled to a heat equation. While the total energy is conserved, the total
entropy serves as a driving functional such that the full coupled system is a
gradient flow. The novelty of the approach is the Onsager structure, which is
the dual form of a gradient system, and the formulation in terms of the
densities and the internal energy. In these variables it is possible to assume
that the entropy density is strictly concave such that there is a unique
maximizer (thermodynamical equilibrium) given linear constraints on the total
energy and suitable density constraints.
We consider two particular systems of this type, namely, a
diffusion-reaction bipolar energy transport system, and a
drift-diffusion-reaction energy
transport system with confining potential. We prove corresponding
entropy-entropy production inequalities with explicitly calculable constants
and establish the convergence to thermodynamical equilibrium, at first in
entropy and further in $L^1$ using Cziszar-Kullback-Pinsker type inequalities.
We derive an optoelectronic model based on a gradient formulation for the relaxation of electron-, hole- and photon-densities to their equilibrium state. This leads to a coupled system of partial and ordinary differential equations, for which we discuss the isothermal and the non-isothermal scenario separately.
Classical gradient systems have a linear relation between rates and driving forces. In generalized gradient systems we allow for arbitrary relations derived from general non-quadratic dissipation potentials. This paper describes two natural origins for these structures.
A first microscopic origin of generalized gradient structures is given by the theory of large-deviation principles. While Markovian diffusion processes lead to classical gradient structures, Poissonian jump processes give rise to cosh-type dissipation potentials.
A second origin arises via a new form of convergence, that we call EDP-convergence. Even when starting with classical gradient systems, where the dissipation potential is a quadratic functional of the rate, we may obtain a generalized gradient system in the evolutionary -limit. As examples we treat (i) the limit of a diffusion equation having a thin layer of low diffusivity, which leads to a membrane model, and (ii) the limit of difusion over a high barrier, which gives a reaction-diffusion system.