Kinetics of the sodium carbonate–sulfur dioxide reaction
Authors:
- 1 September 1987
- journal article
- research article
- Published by Wiley in AIChE Journal
- Vol. 33 (9) , 1522-1532
Abstract
The Kinetics of the SO2‐Na2CO3 reaction were studied at 353 to 413 K and atmospheric pressure with thermal gravimetric analysis data. Since the reaction is very fast, special precautions were taken to operate at conditions such that transport effects did not influence results. The data indicated that Na2SO3 was formed by two paths: direct reaction, and adsorption of SO2 followed by conversion of adsorbed SO2 to adsorbed CO2 and finally desorption to final product. Rate constants were evaluated for each step in the proposed mechanism. Product distribution predicted from the rate constants agreed well with the distribution calculated from the experimental data at temperatures from 353 to 413 K. At 413 K the results suggested a change in mechanism.Keywords
This publication has 13 references indexed in Scilit:
- Kinetics of sodium bicarbonate decompositionAIChE Journal, 1986
- Single‐Pellet, moment method for analysis of gas‐solid reactionsAIChE Journal, 1986
- Analysis of distributed pore closure in gas‐solid reactionsAIChE Journal, 1985
- Modeling of noncatalytic gas‐solid reactionsAIChE Journal, 1982
- A random pore model for fluid‐solid reactions: II. Diffusion and transport effectsAIChE Journal, 1981
- The effect of pore structure on fluid‐solid reactions: Application to the SO2‐lime reactionAIChE Journal, 1981
- The Importance of Pore Structure and Diffusion in the Kinetics of Gas-Solid Non-catalytic Reactions: Reaction of Calcined Limestone with SO2The Chemical Engineering Journal, 1981
- A single‐pore model for gas‐solid noncatalytic reactionsAIChE Journal, 1977
- Reaction of Sulfur Dioxide with Limestone and the Influence of Pore StructureIndustrial & Engineering Chemistry Process Design and Development, 1974
- Kinetics of the reaction between the solid sodium carbonate and the gaseous sulphur dioxide. II. Interpretation of the excess kinetic function by means of a microscopic modelCollection of Czechoslovak Chemical Communications, 1969