A 1-D non-isothermal dynamic model for the thermal decomposition of a gibbsite particle

Amirpiran Amiri*, Andrey V. Bekker, Gordon D. Ingram, Iztok Livk, Nicoleta E. Maynard

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


A 1-D mathematical model describing the thermal decomposition, or calcination, of a single gibbsite particle to alumina has been developed and validated against literature data. A dynamic, spatially distributed, mass and energy balance model enables the prediction of the evolution of chemical composition and temperature as a function of radial position inside a particle. In the thermal decomposition of gibbsite, water vapour is formed and the internal water vapour pressure plays a significant role in determining the rate of gibbsite dehydration. A thermal decomposition rate equation, developed by closely matching experimental data reported previously in the literature, assumes a reaction order of 1 with respect to gibbsite concentration, and an order of -1 with respect to water vapour pressure. Estimated values of the transformation kinetic parameters were k0=2.5×1013mol/(m3s) for the pre-exponential factor, and Ea=131kJ/mol for the activation energy. Using these kinetic parameters, the gibbsite particle model is solved numerically to predict the evolution of the internal water vapour pressure, temperature and gibbsite concentration. The model prediction was shown to be very sensitive to the values of heat transfer coefficient, effective diffusivity, particle size and external pressure, but relatively less sensitive to the mass transfer coefficient and particle thermal conductivity. The predicted profile of the water vapour pressure inside the particle helps explain some phenomena observed in practice, including particle breakage and formation of a boehmite phase.

Original languageEnglish
Pages (from-to)485-496
Number of pages12
JournalChemical Engineering Research and Design
Issue number3
Early online date18 Oct 2012
Publication statusPublished - Mar 2013


  • alumina production
  • distributed dehydration model
  • gibbsite calcination
  • particle breakage
  • water vapour pressure


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