Abstract
Single-pellet moment technique which was initially proposed for the measurement of effective diffusivities in porous catalysts and adsorption rate and equilibrium constants was modified for the analysis of gas-solid reactions. In this technique dynamic version of the Wicke-Kallenbach single-pellet cell was used. A pulse of a tracer gas was introduced into stream flowing over one end face of the pellet. In the modified pulse-double response procedure, experimental moments of the response peaks of both reactant and product gases measured in both top and bottom outlet streams of the single-pellet reactor were used for the evaluation of intrapellet rate and equilibrium parameters. Application of the technique to the reaction of SO 2 with activated soda indicated that the value of Thiele modulus decreased from 6.74 to 0.33 by the increase of fractional conversion of Na 2CO 3 to Na 2SO 3 from zero to 0.63. In this range of conversion values a significant variation in pore structure and also a decrease of effective diffusivity of SO 2 from 0.045 cm 2/s to 0.025 cm 2/s was observed. A cell model which considered the changes in pore length and radius with reaction extent and variations in product layer diffusion resistance was shown to be successfully used in the analysis of experimental observations. A review of single-pellet dynamic reactor studies for catalytic and noncatalytic gas-solid reactions was also given.
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