Biomass pyrolysis TGA assessment with an international round robin

Journal Article (2020)
Author(s)

Andrés Anca-Couce (Graz University of Technology)

C. Tsekos (TU Delft - Large Scale Energy Storage)

Stefan Retschitzegger (BEST – Bioenergy and Sustainable Technologies )

Francesco Zimbardi (ENEA)

Axel Funke (Karlsruhe Institut für Technologie)

Scott Banks (Aston University)

Tzouliana Kraia (Centre for Research and Technology Hellas)

Paula Marques (Unidade de Bioenergia)

Robert Scharler (BEST – Bioenergy and Sustainable Technologies , Graz University of Technology)

W. de Jong (TU Delft - Large Scale Energy Storage)

Norbert Kienzl (BEST – Bioenergy and Sustainable Technologies )

Research Group
Large Scale Energy Storage
Copyright
© 2020 Andrés Anca-Couce, C. Tsekos, Stefan Retschitzegger, Francesco Zimbardi, Axel Funke, Scott Banks, Tzouliana Kraia, Paula Marques, Robert Scharler, W. de Jong, Norbert Kienzl
DOI related publication
https://doi.org/10.1016/j.fuel.2020.118002
More Info
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Publication Year
2020
Language
English
Copyright
© 2020 Andrés Anca-Couce, C. Tsekos, Stefan Retschitzegger, Francesco Zimbardi, Axel Funke, Scott Banks, Tzouliana Kraia, Paula Marques, Robert Scharler, W. de Jong, Norbert Kienzl
Research Group
Large Scale Energy Storage
Volume number
276
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Abstract

The large variations found in literature for the activation energy values of main biomass compounds (cellulose, hemicellulose and lignin) in pyrolysis TGA raise concerns regarding the reliability of both the experimental and the modelling side of the performed works. In this work, an international round robin has been conducted by 7 partners who performed TGA pyrolysis experiments of pure cellulose and beech wood at several heating rates. Deviations of around 20 – 30 kJ/mol were obtained in the activation energies of cellulose, hemicellulose and conversions up to 0.9 with beech wood when considering all experiments. The following method was employed to derive reliable kinetics: to first ensure that pure cellulose pyrolysis experiments from literature can be accurately reproduced, and then to conduct experiments at different heating rates and evaluate them with isoconversional methods to detect experiments that are outliers and to validate the reliability of the derived kinetics and employed reaction models with a fitting routine. The deviations in the activation energy values for the cases that followed this method, after disregarding other cases, were of 10 kJ/mol or lower, except for lignin and very high conversions. This method is therefore proposed in order to improve the consistency of data acquisition and kinetic analysis of TGA for biomass pyrolysis in literature, reducing the reported variability.