In situ monitoring of hydrogen loss during pyrolysis of wood by neutron imaging

Frederik Ossler, Louis J. Santodonato, Jeffrey M. Warren, Charles E.A. Finney, Jean Christophe Bilheux, Rebecca A. Mills, Harley D. Skorpenske, Hassina Z. Bilheux

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Hydrogen is an element of fundamental importance for energy but hard to quantify in bulk materials. Neutron radiography was used to map in situ loss of elemental hydrogen from beech tree wood samples during pyrolysis. The samples consisted of three wood cylinders (finished dowel or cut branch) of approximately 1 cm in length. The samples were pyrolyzed under vacuum in a furnace vessel that was placed inside a cold neutron imaging beamline using a temperature ramp of 5 °C/min from ambient up to 400 °C. Neutron radiographs with exposures of 30 s were sequentially recorded with a charge-coupled device over the course of the experiment. Relative absorbance/scattering of the neutron beam by each sample was based on intensity (or brightness) values as a function of pixel position. The much larger neutron cross section for hydrogen compared to carbon and oxygen enables almost direct conversion of neutron attenuation into sample hydrogen content for each time step during the pyrolysis experiment. Target and vessel temperatures were recorded concurrently with collection of the radiographs so that changes could be directly correlated to different states of pyrolysis. The most visible change appeared at the initial phase of the 400 °C plateau as evidenced by strong hydrogen loss and primarily diametric shrinking of the samples. The loss of elemental hydrogen between initial and final states of pyrolysis was estimated to be about 70%.

Original languageEnglish
Pages (from-to)1273-1280
Number of pages8
JournalProceedings of the Combustion Institute
Volume37
Issue number2
DOIs
StatePublished - 2019

Funding

We want to thank Göran Carlström and Daniel Topgaard for helpful discussions regarding magnentic resonance imaging. Frederik Ossler acknowledges the financial support by the Swedish Energy Agency through the Centre of Combustion Science and Technology (CECOST) and the Lund Laser Centre (LLC). This research used resources at the High Flux Isotope Reactor, a DOE Office of Science User Facility operated by the Oak Ridge National Laboratory. This research was also supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research. Oak Ridge National Laboratory is managed by UT-Battelle, LLC, for the U.S. Department of Energy under contract DE-AC05-1008 00OR22725. The views expressed in this article do not necessarily represent the views of the U.S. Department of Energy or the United States Government.

FundersFunder number
Centre of Combustion Science and Technology
Lund Laser Centre
U.S. Department of Energy
Office of Science
Biological and Environmental Research
Oak Ridge National LaboratoryDE-AC05-1008 00OR22725
Energimyndigheten

    Keywords

    • Biomass
    • Neutron imaging
    • Pyrolysis

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