The interpretation of the experimental self-diffusion data on normal and supercooled water has been revisited in the light of both the recently reported evidence for a temperature-dependent H-bond cooperativity and the free-volume fluctuations within the water percolative patches. The proposed model, which is consistent wth the presence of a continuity of states between liquid and solid phases, was found to fit the NMR experimental data to an accuracy comparable to that obtained by a power law.
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Lamanna et al. (1992) studied this question.
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