Abstract
Recent measurements of the vapor pressures of He3He4 liquid solutions by Daunt and Heer and by Sommers are used to evaluate the solution non-ideality, for the calculation of which the large deviations of the vapor from ideality are taken into account. Estimation of the standard chemical potential of normal He4 at temperatures below the lambda-point is discussed. Agreement of excess chemical potentials of He4 above the lambda-point and the values obtained from the simple theory demonstrates the usefulness of the theory in discussions of effect of nonideality on the shift of the lambda-point with He3 concentration.

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