抄録
Viscosity measurements were made on aqueous solutions of LiCl, Me4NCl, Et4NCl, Me3NBeCl, Et3NBeCl and Me2NBe2Cl in the concentration range 0-3M. The viscosity B coefficients, which were calculated by Vand equation developed for concentrated suspensions, were shown to correlate with the B coefficient of the Jones-Dole equation for dilute solution of the salts. The values of Ve were calculated according to the model of Breslau-Miller. The behavior pattern obtained of Ve as a function of concentration gave indications of the hydration behavior of concentrated solution of the salts. It was suggested that the additivity rule for the B coefficient and for the value of Ve can be applied to the solution of salt mixtures.
Chemical shift of water proton was measured on aqueous solutions of LiCl, Me4NCl, Et4NCl, Me3NBeCl and Et3NBeCl in the concentration range 0-2M. The upfield shift of the water proton decreased in the order, Me4NCI<Et4NCl<Me3NBeCl. This order was consistent with an increase in water structure promotion. The chemical shift of water proton (Δν) was fitted to the equation Δν=am+bm2. It was suggested that additivity rule for the chemical shift of the water proton can not be applied to solutions of salt mixtures, except Me4NCl-Et4NCl mixtures.