The diffusion-limited reaction nA +mB → C is studied both for homogeneous and inhomogeneous initial conditions. For the homogeneous case, microscopic arguments are given which allow one to decide when the kinetics is anomalous. These predictions are confirmed by numerical simulations. For the inhomogeneous case, a front is formed, whose properties can be described by scaling theory. Numerical simulations show that the fluctuations play an important role only in one dimension, provided that n+m ⩽ 3 and play a marginal role in two dimensions for n = m = 1
We consider the properties of the diffusion-controlled reaction A+B to OE in the steady state, where...
We study theoretically and numerically the steady state diffusion controlled reaction A+B→∅, where c...
Fluctuations are known to radically alter the behaviour of reaction-diffusion systems. Below a certa...
We study the three component Reaction-Diffusion systems with and without precipitation and crystal g...
Properties of reaction zones resulting from A+B -> C type reaction-diffusion processes are investiga...
The A+B→{circled division slash} diffusion-limited reaction, with equal initial densities a(0)=b(0)=...
The A +B ~ ~ diffusion-limited reaction, with equal initial densities a(0)= b(0)=n0, is studied by ...
Extensive simulations are performed of the diffusion-limited reaction A+B→0 in one dimension, with i...
We investigate the A + B = 0 bimolecular chemical reaction taking place in low-dimensional spaces wh...
The small-time asymptotic properties of the reaction front formed by a reaction A+B→C coupled to dif...
A field-theoretical model describing simple one-species reaction-diffusion systems [A+A→O (inert) or...
The conditions for macroscopic segregation of A and B in a steady-state A+B → 0 reaction are studied...
Abstract. Fluctuations in diffusion-controlled reactions lack the necessary features for a mesoscopi...
Many chemical reactions occur in a viscous solvent and are diffusion-limited, making a mean-field or...
The kinetics laws of diffusion-controlled chemical reactions are drastically different from the conv...
We consider the properties of the diffusion-controlled reaction A+B to OE in the steady state, where...
We study theoretically and numerically the steady state diffusion controlled reaction A+B→∅, where c...
Fluctuations are known to radically alter the behaviour of reaction-diffusion systems. Below a certa...
We study the three component Reaction-Diffusion systems with and without precipitation and crystal g...
Properties of reaction zones resulting from A+B -> C type reaction-diffusion processes are investiga...
The A+B→{circled division slash} diffusion-limited reaction, with equal initial densities a(0)=b(0)=...
The A +B ~ ~ diffusion-limited reaction, with equal initial densities a(0)= b(0)=n0, is studied by ...
Extensive simulations are performed of the diffusion-limited reaction A+B→0 in one dimension, with i...
We investigate the A + B = 0 bimolecular chemical reaction taking place in low-dimensional spaces wh...
The small-time asymptotic properties of the reaction front formed by a reaction A+B→C coupled to dif...
A field-theoretical model describing simple one-species reaction-diffusion systems [A+A→O (inert) or...
The conditions for macroscopic segregation of A and B in a steady-state A+B → 0 reaction are studied...
Abstract. Fluctuations in diffusion-controlled reactions lack the necessary features for a mesoscopi...
Many chemical reactions occur in a viscous solvent and are diffusion-limited, making a mean-field or...
The kinetics laws of diffusion-controlled chemical reactions are drastically different from the conv...
We consider the properties of the diffusion-controlled reaction A+B to OE in the steady state, where...
We study theoretically and numerically the steady state diffusion controlled reaction A+B→∅, where c...
Fluctuations are known to radically alter the behaviour of reaction-diffusion systems. Below a certa...