Abstract
The diffusion of He3 and He4 in vitreous silica was experimentally measured in the temperature range 100-760°C. The ratio of the diffusion coefficients is given by D(He3)D(He4)=(1.205±0.003) exp[(131±7calgat.)RT]. These results cannot be explained by classical diffusion theory, which does not predict an isotope effect in the activation energy for diffusion. The quantum corrections proposed by LeClaire for the special case of low-atomic-mass isotope diffusion satisfactorily explain the observed results.

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