Multispecies reaction-diffusion systems

Multispecies reaction-diffusion systems, for which the time evolution equation of correlation functions become a closed set, are considered. A formal solution for the average densities is found. Some special interactions and the exact time dependence of the average densities in these cases are also studied. For the general case, the large time behaviour of the average densities has also been obtained.Comment: LaTeX file, 15 pages, to appear in Phys. Rev.

Mass transfer and chemical reaction in gas-liquid-liquid systems

Gas-liquid-liquid reaction systems may be encountered in several important fields of application as e.g. hydroformylation, alkylation, carboxylation, polymerisation, hydrometallurgy, biochemical processes and fine chemicals manufacturing. However, the reaction engineering aspects of these systems have only been considered occasionally. For systems with very slow reaction kinetics this is not surprising, as the three phases will be at physical equilibrium. In reaction systems with fast parallel and consecutive reactions the effects of mass transfer and mixing on the product yield can be significant. A fascinating example of such a reaction system is the Koch synthesis of Pivalic Acid. In this work this reaction system was chosen as model system to study these effects

Reaction-diffusion systems with constant diffusivities: conditional symmetries and form-preserving transformations

Q-conditional symmetries (nonclassical symmetries) for a general class of two-component reaction-diffusion systems with constant diffusivities are studied. Using the recently introduced notion of Q-conditional symmetries of the first type (R. Cherniha J. Phys. A: Math. Theor., 2010. vol. 43., 405207), an exhaustive list of reaction-diffusion systems admitting such symmetry is derived. The form-preserving transformations for this class of systems are constructed and it is shown that this list contains only non-equivalent systems. The obtained symmetries permit to reduce the reaction-diffusion systems under study to two-dimensional systems of ordinary differential equations and to find exact solutions. As a non-trivial example, multiparameter families of exact solutions are explicitly constructed for two nonlinear reaction-diffusion systems. A possible interpretation to a biologically motivated model is presented

Reaction-diffusion systems and nonlinear waves

The authors investigate the solution of a nonlinear reaction-diffusion equation connected with nonlinear waves. The equation discussed is more general than the one discussed recently by Manne, Hurd, and Kenkre (2000). The results are presented in a compact and elegant form in terms of Mittag-Leffler functions and generalized Mittag-Leffler functions, which are suitable for numerical computation. The importance of the derived results lies in the fact that numerous results on fractional reaction, fractional diffusion, anomalous diffusion problems, and fractional telegraph equations scattered in the literature can be derived, as special cases, of the results investigated in this article.Comment: LaTeX, 16 pages, corrected typo

Resonantly Forced Inhomogeneous Reaction-Diffusion Systems

The dynamics of spatiotemporal patterns in oscillatory reaction-diffusion systems subject to periodic forcing with a spatially random forcing amplitude field are investigated. Quenched disorder is studied using the resonantly forced complex Ginzburg-Landau equation in the 3:1 resonance regime. Front roughening and spontaneous nucleation of target patterns are observed and characterized. Time dependent spatially varying forcing fields are studied in the 3:1 forced FitzHugh-Nagumo system. The periodic variation of the spatially random forcing amplitude breaks the symmetry among the three quasi-homogeneous states of the system, making the three types of fronts separating phases inequivalent. The resulting inequality in the front velocities leads to the formation of ``compound fronts'' with velocities lying between those of the individual component fronts, and ``pulses'' which are analogous structures arising from the combination of three fronts. Spiral wave dynamics is studied in systems with compound fronts.Comment: 14 pages, 19 figures, to be published in CHAOS. This replacement has some minor changes in layout for purposes of neatnes

From chemical Langevin equations to Fokker-Planck equation: application of Hodge decomposition and Klein-Kramers equation

The stochastic systems without detailed balance are common in various chemical reaction systems, such as metabolic network systems. In studies of these systems, the concept of potential landscape is useful. However, what are the sufficient and necessary conditions of the existence of the potential function is still an open problem. Use Hodge decomposition theorem in differential form theory, we focus on the general chemical Langevin equations, which reflect complex chemical reaction systems. We analysis the conditions for the existence of potential landscape of the systems. By mapping the stochastic differential equations to a Hamiltonian mechanical system, we obtain the Fokker-Planck equation of the chemical reaction systems. The obtained Fokker-Planck equation can be used in further studies of other steady properties of complex chemical reaction systems, such as their steady state entropies.Comment: 6 pages, 0 figure, submitted to J. Phys. A: Math. Theo

Reaction-Diffusion Systems as Complex Networks

The spatially distributed reaction networks are indispensable for the understanding of many important phenomena concerning the development of organisms, coordinated cell behavior, and pattern formation. The purpose of this brief discussion paper is to point out some open problems in the theory of PDE and compartmental ODE models of balanced reaction-diffusion networks.Comment: A discussion paper for the 1st IFAC Workshop on Control of Systems Governed by Partial Differential Equation