Heat Capacity and Other Properties of Body-Centered CubicHe4

Abstract
The heat capacity at constant volume, Cv, of bcc He4 has been measured for a number of molar volumes covering most of the bcc region of the phase diagram. The results can be represented to within 3% of Cv by a constant Debye Θ of 16.95°K. Using the discontinuities in the heat capacity at the phase boundaries measured in this and in previous work, the compressibility κ is found to be (3.8±0.2)×103 atm1 and substantially independent of temperature, while values of the expansion coefficient α found by the same method are between 5×103 and 13×103 deg1. The values of α are consistent with a Gruneisen equation with a Gruneisen constant γ2.6, the value found previously for hcp He4. The latent heats at constant volume at the lower and upper triple points T1 and T2 have been measured as a function of volume and give for the maximum entropy change at T1, where (hcp+liq) → (bcc), the value ΔS1R=(9±1)×103. The maximum entropy change at T2, where bcc → (hcp+liq), has the value ΔS2R=(32±2)×103. The triple-point temperatures were found to be T1=1.463±0.002°K and T2=1.7715±0.001°K. The intersection of the λ line with the bcc phase boundary has been confirmed to be ∼10 mdeg below the upper triple point. The entropy of the bcc phase at the transition line has been computed from the heat-capacity results and the latent-heat measurements, and is found to vary from SR=0.037±0.002 at T1 to SR=0.068±0.003 at T2. The relation between S and Cv is the same as for the other low-pressure structures of solid He3 and He4, indicating that the variation of Θ with T and therefore the lattice spectra are similar. On the supposition that bcc He4 is indeed like the other forms of solid helium, it is estimated that bcc He4 would have a Debye Θ at 0°K, Θ0, of 21°K for a molar volume of 21 cm3. This value of Θ0, when compared with the measured velocity of sound, indicates that bcc He4 is elastically highly anisotropic, in agreement with the recent theory of Nosanow and Werthamer.

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