| Abstract: | The self-diffusion of water and hexadecane in medium and coarse sands from glacial sand deposits in central Germany were investigated by pulsed field gradient nuclear magnetic resonance (PFG NMR). Due to the restriction of the diffusion path at the pore/grain interface, the measured apparent self-diffusion coefficients (D(Δ)) in the pore space depend on the observation time (Δ) in the PFG NMR experiment. Although the bulk self-diffusion coefficients of water and hexadecane differ by about one order of magnitude, the apparent self-diffusion coefficients in the pore space obey the same characteristic time-behaviour, which depends only on geometrical properties of the pore system. Using the “short-time diffusion” model, surface-to-volume (S/V) ratios and inherent self-diffusion coefficients (D0) of the pore fluids were extracted from these diffusion measurements. The S/V ratios obtained are independent of the pore fluid used and agree with known geometrical properties of the sand grains. Moreover, the D0 values are consistent with the corresponding bulk self-diffusion coefficients measured separately. In contrast to these results of PFG NMR, simultaneous investigations of longitudinal (T1) nuclear magnetic relaxation reveal that the relaxation time of the pore fluid is a less suitable parameter for a quantitative estimation of geometrical properties of the pore/grain interface in these unconsolidated sediments since it depends on chemical properties of the fluid/grain interface. |
