Issue 0, 1978

Sorption kinetics and time-lag theory. Part 1.—Constant diffusion coefficient

Abstract

The time-lag concept has been applied to sorption kinetics so as to provide an alternative procedure for obtaining diffusion coefficients D, in systems where D is a constant. From the graph of fractional approach to equilibrium, η(t), [0 ⩽η(t) < 1] against tν(ν > 0), the quantity I[triple bond, length as m-dash] [graphic omitted] η(t) d(tν)(obtained as the area beneath the curve) may be found as a function of tν. For large t the curve of I against tν approaches a linear asymptote which intersects the axis of tν to give a time-lag, Lν, where Lν= [graphic omitted] [1 –η(t)]d(tν).

Explicit equations for Lν have been obtained and investigated for various geometries of the diffusion media. Those for ν=½ and ν= 1 in particular often lead to simple relations from which D can be evaluated. Both constant pressure and constant volume sorption kinetics have been considered, in the latter instance when Henry's law governs the sorption isotherm.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 2, 1978,74, 40-56

Sorption kinetics and time-lag theory. Part 1.—Constant diffusion coefficient

R. Ash, R. M. Barrer and R. J. B. Craven, J. Chem. Soc., Faraday Trans. 2, 1978, 74, 40 DOI: 10.1039/F29787400040

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