The intrinsic thermal decomposition kinetics of SrCO3 by a nonisothermal technique |
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Authors: | I Arvanitidis Du Sichen S Seetharaman H Y Sohn |
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Affiliation: | (1) Division of Theoretical Metallurgy, Royal Institute of Technology, S-100 44 Stockholm, Sweden;(2) the Department of Metallurgical Engineering, University of Utah, 84112 Salt Lake City, UT |
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Abstract: | The kinetics of the decomposition of SrCO3 in argon to SrO and CO2 were studied in the temperature range 1000 to 1350 K. The thermal decomposition was followed simultaneously by thermogravimetric
analysis (TGA) and differential thermal analysis (DTA) during linear heating. By using a nonisothermal method, the complete
rate expression was determined from a relatively small number of experimental runs. Shallow beds of fine synthetic powder
as well as thin flakes of pressed powder were employed to obtain the kinetics of decomposition in the absence of heat- and
mass-transfer effects. The thermal decomposition started at about 1000 K. The recommended rate expression for the SrCO3 decomposition is where α is the ratio between the actual weight change and the theoretical final weight change, dα/dt is the time derivative of α, B is a rate constant in s−1, E is the activation energy in J·mol−1, R is the gas constant in J·K−1·mol−1, T is the temperature in kelvin, and n is a factor depending on the geometry of the particles. The activation energy, E, for the decomposition of SrCO3 was evaluated to be 210 kJ/mol. Curves of calculated α vs temperature agree well with the experimental results. |
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