Modelling of catalytic oxidation of NH3 and reduction of NO on limestone during sulphur capture

Publication: Research - peer-reviewJournal article – Annual report year: 1996

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A theoretical study of the complex transient system of simultaneous sulphur capture and catalytic reactions of N-containing compounds taking place on a single limestone particle is conducted. The numerical technique developed previously by the authors (Kiil et al. 1994) based on collocation on moving finite elements is used to solve the model equations. To our knowledge, this is the first serious attempt to model such transient systems in detail. The particle is divided into moving zones, described by the reaction between limestone and SO2, and each zone is assigned a certain catalytic activity with respect to each species involved. An existing particle model, the Grain-Micrograin Model, which simulates sulphur capture on limestone under oxidizing conditions is considered in the modelling. Simulation results in good qualitative agreement with experimental data are obtained here for the catalytic chemistry of NH3 during simultaneous sulphur capture on a Stevns Chalk particle. The reduction of NO by NH3 over CaSO4 (which is the product of the reaction between SO2, O2 and limestone) was found to be important because this reaction could explain the change in selectivity with increased solid conversion observed experimentally. Simulations also suggested that it may be advantageous with respect to the emission of NO to use smallinstead of big limestone particles for desulphurisation in fluidised bed combustors due to the ways different sized particles capture SO2.
Original languageEnglish
JournalChemical Engineering Science
Publication date1996
Volume51
Journal number4
Pages587-601
ISSN0009-2509
StatePublished
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