• Sanz, Francisco Javier Escudero
• Guizani, Chamseddine
• Gadiou, R.
• Jeguirim, M.
• Salvador, Sylvain

Abstract

Despite the huge literature on biomass char gasification with CO2 or H2O, ambiguity still hovers over the issue of char gasification in complex atmospheres. Gas alternation gasification experiments, in which the reacting gas is changed during the reaction, were performed with CO2/H2O at 900 degrees C for small (200 mu m) and large (13 mm) Low Heating Rate (LHR) beech wood char particles to assess the potential influences that CO2 and H2O can have on each other during the char gasification reaction. The results showed no influence of a first gasification atmosphere on the char reactivity under the second one. The char reactivity to a specific gas at a certain conversion level was the same as if the gasification reaction was operated from the beginning with the same atmosphere composition. The purpose of this paper is to bring understanding keys to this lack of influence of previous gasification conditions on the char reactivity. Characterization of the chars throughout the conversion by measuring the total surface area and the active surface area was first performed. Then a transport limitation analysis based on the Thiele modulus was considered. It was concluded that the two gasses develop different porosities in the char, however, the Thiele modeling results and active surface area analysis indicate respectively that gasses diffuse preferentially in large macro-pores and that the concentration of active sites evolves similarly during both gasification reactions. This similarity in the diffusion mechanism as well as in the evolution of the concentration of active sites could be a plausible explanation for the only-dependent conversion reactivity observed in the gas alternation gasification experiments.

Topics

• impedance spectroscopy
• pore
• surface
• experiment
• wood
• gasification