Viscosities and densities of highly concentrated aqueous MOH solutions (M+= Na+, K+, Li+, Cs+, (CH3)(4)N+) at 25.0 degrees C

The absolute (dynamic) viscosities (eta) and densities (rho) of carbonate-f ree aqueous tetramethylammonium and alkali metal hydroxides have been deter mined up to saturation concentrations ([NaOH] less than or equal to 19.1 M, [KOH] less than or equal to 14.1 M, [LiOH] less than or equal to 4.8 M, [C sOH] less than or equal to 14.8 M, and [(CH3)(4)NOH] less than or equal to 4.2 M) at 25.00 degrees C using a Ubbelohde viscometer and a vibrating tube densitometer, respectively. The viscosities are believed to be precise to within 0.1% and the densities to within 5 x 10(-6) g cm(-3). Densities of i soplethic MOH solutions increase in the order of (CH3)(4)N+ < Li+ < Na+ < K + << Cs+. Viscosities for [MOH] < 4 M solutions increase in the reverse ord er, but the viscosities of CsOH solutions become extremely large at very hi gh concentrations. The shape of the density vs concentration function of (C H3)(4)NOH solutions is also quite different when compared with the alkali m etal hydroxide solutions. Density data were fitted up to the highest concen trations using the Masson equation. Viscosity vs concentration functions ar e represented in the form of a fifth-order (empirical) polynomial.