Abstract
The attenuation α, the velocity u, and the dispersion D=u(ω)u(0) of first sound have been determined in He3-He4 mixtures (molar He3 concentrations X3=0, 0.070, 0.194, 0.377, and 0.517) at frequencies 2.3ω2π627 kHz, and in the temperature range 1 μK ≤ |TTλ| ≤ 10 mK. From the measured velocities we calculate the thermodynamic velocity u(0), as well as (SP)λ and (VP)λ. The attenuation and the dispersion are considerably reduced when the He3 concentration is increased. They are interpreted as arising from a relaxation process occurring only below Tλ, and a fluctuation process occurring on both sides of the λ transition. Both contributions have about equal strength. The strength AR of the relaxation process decreases nearly three orders of magnitude with increasing X3 in our concentration range. Using the obtained relaxation time τ=τ0tx (with t=|TTλ|Tλ), and published data for the correlation length ξ, and for the second-sound velocity u2, we find τ=ξu2 for T<Tλ. The amplitude