CO2 gasification of chars prepared from wood and forest residue: A kinetic study

Liang Wang, Judit Sandquist, Gabor Varhegyi, Berta Matas Güell

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27 Citations (Scopus)

Abstract

The CO2 gasification of chars prepared from Norway spruce and its forest residue was investigated in a thermogravimetric analyzer (TGA) at slow heating rates. The volatile content of the samples was negligible; hence the gasification reaction step could be studied alone, without the disturbance of the devolatilization reactions. Six TGA experiments were carried out for each sample with three different temperature programs in 60 and 100% CO2. Linear, modulated, and constant-reaction rate (CRR) temperature programs were employed to increase the information content available for the modeling. The temperatures at half of the mass loss were lower in the CRR experiments than in the other experiments by around 120 C. A relatively simple, well-known reaction kinetic equation described the experiments. The dependence on the reacted fraction as well as the dependence on the CO2 concentration were described by power functions (n-order reactions). The evaluations were also carried out by assuming a function of the reacted fraction that can mimic the various random pore/random capillary models. These attempts, however, did not result in an improved fit quality. Nearly identical activation energy values were obtained for the chars made from wood and forest residues (221 and 218 kJ/mol, respectively). Nevertheless, the forest residue char was more reactive; the temperatures at half of the mass loss showed 20-34 C differences between the two chars at 10 C/min heating rates. The assumption of a common activation energy, E, and a common reaction order, ν, on the CO2 concentration for the two chars had only a negligible effect on the fit quality.

Original languageEnglish
Pages (from-to)6098-6107
Number of pages10
JournalEnergy and Fuels
Volume27
Issue number10
DOIs
Publication statusPublished - Oct 17 2013

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ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Fuel Technology
  • Energy Engineering and Power Technology

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