NMR Spin-Rotation Relaxation and Diffusion of Methane

Abstract

The translational-diffusion coefficient $D_T$ and the spin-rotation contribution to the $^1$H NMR relaxation time $T_{1J}$ for methane (CH$_4$) are investigated using MD (molecular dynamics) simulations, over a wide range of densities $ρ$ and temperatures $T$, spanning the liquid, supercritical, and gas phases. The simulated $D_T$ agree well with measurements, without any adjustable parameters in the interpretation of the simulations. A minimization technique is developed to compute the angular-velocity for non-rigid spherical molecules, which is used to simulate the autocorrelation function $G_{\!J}(t)$ for spin-rotation interactions. With increasing $D_T$ (i.e. decreasing $ρ$), $G_{\!J}(t)$ shows increasing deviations from the single-exponential decay predicted by the Langevin theory for hard spheres, and the deviations are quantified using inverse Laplace transforms of $G_{\!J}(t)$. $T_{1J}$ is derived from $G_{\!J}(t)$ using the kinetic model "km" for gases ($T_{1J}^{km}$), and the diffusion model "dm" for liquids ($T_{1J}^{dm}$). $T_{1J}^{km}$ shows better agreement with $T_1$ measurements at higher $D_T$, while $T_{1J}^{dm}$ shows better agreement with $T_1$ measurements at lower $D_T$. $T_{1J}^{km}$ is shown to dominate over the MD simulated $^1$H-$^1$H dipole-dipole relaxation $T_{1RT}$ at high $D_T$, while the opposite is found at low $D_T$. At high $D_T$, the simulated spin-rotation correlation-time $τ_J$ agrees with the kinetic collision time $τ_K$ for gases, from which a new relation $1/T_{1J}^{km} \propto D_T$ is inferred, without any adjustable parameters.