The large diffusion coefficients of gases result in significant spin motion
during the application of gradient pulses that typically last a few millis
econds in most NMR experiments. In restricted environments, such as the lun
g, this rapid gas diffusion can lead to violations of the narrow pulse appr
oximation, a basic assumption of the standard Stejskal-Tanner NMR method of
diffusion measurement. We therefore investigated the effect of a common, b
iologically inert buffer gas, sulfur hexafluoride (SF6), on Xe-129 NMR and
diffusion. We found that the contribution of SF6 to Xe-129 T-1 relaxation i
n a 1:1 xenon/oxygen mixture is negligible up to 2 bar of SF6 at standard t
emperature. We also measured the contribution of SF6 gas to Xe-129 T-2 rela
xation, and found it to scale inversely with pressure, with this contributi
on approximately equal to 1 s for 1 bar SF6 pressure and standard temperatu
re. Finally, we found the coefficient of Xe-129 diffusion through SF6 to be
approximately 4.6 x 10(-6) m(2)s(-1) for 1 bar pressure of SF6 and standar
d temperature, which is only 1.2 times smaller than the Xe-129 self diffusi
on coefficient for 1 bar Xe-129 pressure and standard temperature. From the
se measurements we conclude that SF6 will not sufficiently reduce Xe-129 di
ffusion to allow accurate surface-area/volume ratio measurements in human a
lveoli using time-dependent gas diffusion NMR.