Abstract
The relaxation times T1 and T2 of He3 nuclei in pure liquid He3 and in liquid He3 - He4 mixtures have been measured in the temperature range 0.9°K<T<2.6°K. Reproducible relaxation times longer than those previously reported have been obtained by employing an extensive cleaning procedure. The Pyrex sample chamber and filling capillary were repeatedly cleaned in the presence of several mm of pure He4 by heating the glass to almost melting and, at the same time, touching the glass surface with a Tesla coil. This coil creates a high-frequency discharge which drives absorbed gases off the wall. T1 for pure He3 was found to have the value and the temperature dependence predicted by the modified Bloembergen-Purcell-Pound theory to within ±3%. T1 is proportional to the diffusion coefficient, and increases from 350 sec at 1.0°K to 450 sec at 1.8°K. T2 was found to be approximately equal to T1. These long relaxation times were significantly shortened by contamination of the clean chamber with air or by inadequate purification of the He3 sample. Since the work on pure He3 showed that wall effects could be minimized by cleaning, it was considered of interest to measure T1 in He3 - He4 mixtures. The relaxation times of a 33% He3 solution were determined in an extensively cleaned system. Above the λ point, T1 is about 50% greater than for pure He3, while just below this temperature it increases sharply by about 15%. Measurements of T1 of other mixtures were made in partially cleaned systems. The results were affected by wall relaxation and bulk impurities. Some conclusions about T1 are drawn from these data.