Simple Binary Collision Model for Van Hove'sGs(r, t)

Abstract
It is noted that the Van Hove self-correlation function Gs(r, t) for a dilute fluid is determined by a linearized Boltzmann equation identical to that occuring in the theory of neutron diffusion. A simple model for the collision integral, in which a molecule emerges from a collision with a Maxwellian distribution, allows some interesting analytic results to be obtained. The double Fourier transform Ss(κ, ω), of Gs(r, t) is expressible in terms of the probability integral for complex arguments. Since Ss(κ, ω) is directly proportional to the Mössbauer line shape, the transition of the line shape from Doppler broadening to simple diffusion broadening is explicitly exhibited as a function of momentum transfer. The spatial moments of Gs(r, t) are calculated as a function of time. The model used gives the same mean-square displacement as does the Langevin equation. The resulting Gs(r, t) is not, however, Gaussian as is shown by the mean fourth power of the displacement which is 25% greater at intermediate times than would be predicted by the Langevin equation. The non-Gaussian effects lead to an appreciable narrowing of Ss(κ, ω) for intermediate values of κ.