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Kinetic Behavior of Torrefied Biomass in an Oxidative Environment

Sammendrag

The combustion of four torrefied wood samples and their feedstocks (birch and spruce) was studied at slow heating programs, under well-defined conditions by thermogravimetry (TGA). Particularly low sample masses were employed to avoid the self-heating of the samples due to the huge reaction heat of the combustion. Linear, modulated and constant-reaction rate (CRR) temperature programs were employed in the TGA experiments in gas flows of 5 and 20% O2. In this way the kinetics was based on a wide range of experimental conditions. The ratio of the highest and lowest peak maxima was around 50 in the experiments used for the kinetic evaluation. A recent kinetic model of Várhegyi et al. [Energy & Fuels 2012, 26, 1323-1335] was employed with modifications. This model consists of two devolatilization reactions and a successive char burn-off reaction. The cellulose decomposition in the presence of oxygen has a self-accelerating (autocatalytic) kinetics. The decomposition of the non-cellulosic parts of the biomass was described by a distributed activation model. The char burn-off was approximated by power-law (n-order) kinetics. Each of these reactions has its own dependence on the oxygen concentration that was expressed by power-law kinetics, too. The complexity of the applied model reflects the complexity of the studied materials. The model contained 15 unknown parameters for a given biomass. Part of these parameters could be assumed common for the six samples without a substantial worsening of the fit quality. This approach increased the average experimental information for an unknown parameter by a factor of 2 and revealed the similarities in the behavior of the different samples. Copyright © 2013 American Chemical Society

Kategori

Vitenskapelig artikkel

Oppdragsgiver

  • Research Council of Norway (RCN) / 193817

Språk

Engelsk

Forfatter(e)

Institusjon(er)

  • Norges teknisk-naturvitenskapelige universitet
  • SINTEF Energi AS / Termisk energi
  • Ungarn

År

2013

Publisert i

Energy & Fuels

ISSN

0887-0624

Forlag

American Chemical Society (ACS)

Årgang

27

Hefte nr.

2

Side(r)

1050 - 1060

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