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The heavy isotope of hydrogen. The Liversidge Lecture, 1934

Published online by Cambridge University Press:  24 October 2008

R. H. Fowler
Affiliation:
Trinity College

Extract

When I was invited by Christ's College to deliver this year the Liversidge Lecture, it was indicated to me kindly but firmly that I was to talk about heavy hydrogen. I appreciate most deeply the honour you have done me by this invitation, especially by coupling my name (as it were) with this distinguished American newcomer to physical and chemical science. I cannot claim myself to be much more than an interested spectator of the rapid progress which has already been made in the study of this new substance, and the facts that I shall comment on (and the many others which time will force me to neglect) have been established by the collaboration of many workers—some of them our colleagues here, who would be much better qualified to speak at first hand about heavy hydrogen than I. Professor Liversidge laid it down in his deed of gift that his lecturer shall not deal with generalities or give a mere review of his subject, or give an instructional lecture suitable for undergraduates, but shall primarily try to encourage research and to stimulate himself and his audience to think, and to acquire new knowledge. In trying to fulfil his wish I shall not therefore catalogue all the new interesting properties of heavy hydrogen; this will mean, I fear, that I can make little or no further reference to its extremely exciting properties as an atomic projectile in disintegrating lithium and other nuclei, or to the equally exciting prospect that heavy water may have entirely distinct biological properties from ordinary water, being even lethal to many organisms, or to the wonderful possibilities of the new complex organic chemistry.

Type
Research Article
Copyright
Copyright © Cambridge Philosophical Society 1934

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References

* Lewis, G. N. and Macdonald, , J. Chem. Physics, vol. 1, p. 341 (1933)CrossRefGoogle Scholar.

* By a somewhat different use of the same fundamental relations, Lewis and Macdonald first found x = 1/6500 for Berkeley tap water. More recent work by a more accurate method by Bleakney and Gould, using measurements of relative abundance of H and D in a positive ray apparatus, give x = 1/5000. It is easy to understand why in many cases the earlier mistaken value 1/30,000 has been reported. If the hydrogen examined is prepared by electrolysis of water from a recently established cell with the diplogen content will in fact be 1/30,000.

* Bernal: “Lattice constants of ice” (unpublished). Other data from Lewis, G. N. and Macdonald, , J. Amer. Chem. Soc. vol. 55, p. 3057 (1933)CrossRefGoogle Scholar, and other references, that journal and year.

* Rayleigh, , Scientific Papers, vol. 3, p. 397Google Scholar. I have slightly recast Rayleigh's paper by taking explicit account in the factor g (r) of the average radial distribution of neighbours round a given molecule.

* Hückel, , Zeits. f. Elektrochemie, vol. 34, p. 546 (1928).Google Scholar

* I owe to Dr Harteck the most illuminating remark that perhaps the failure to achieve a high separation factor with some electrodes, particularly copper when oxidized or dirty, may be due to the breakdown of the diffusion process in the dirty layer. If this layer eliminates the diffusive readjustment, as it might well do, then the enrichment factor will be controlled by the mobilities as discussed in the text.

* But not necessarily so even then. See Bell, , Nature, Jan. 6 (1934).Google Scholar