Catalytic gasification of glycerol in supercritical water

dc.contributor.author
May Masnou, Anna
dc.contributor.author
Salvadó i Rovira, Joan
dc.contributor.author
Torras, Carles
dc.contributor.author
Montané i Calaf, Daniel
dc.date.issued
2015-02-11T10:06:27Z
dc.date.issued
2015-02-11T10:06:27Z
dc.date.issued
2010
dc.date.issued
2015-02-11T10:06:27Z
dc.identifier
1385-8947
dc.identifier
https://hdl.handle.net/2445/62753
dc.identifier
625735
dc.description.abstract
The conversion of glycerol in supercritical water (SCW) was studied at 510-550 °C and a pressure of 350 bars using both a bed of inert and non-porous ZrO2 particles (hydrothermal experiments), and a bed of a 1% Ru/ZrO2 catalyst. Experiments were conducted with a glycerol concentration of 5 wt% in a continuous isothermal fixed-bed reactor at a residence time between 2 and 10 s. Hydrothermolysis of glycerol formed water-soluble products such as acetaldehyde, acetic acid, hydroxyacetone and acrolein, and gases like H2, CO and CO2. The catalyst enhanced the formation of acetic acid, inhibited the formation of acrolein, and promoted gasification of the glycerol decomposition products. Hydrogen and carbon oxides were the main gases produced in the catalytic experiments, with minor amounts of methane and ethylene. Complete glycerol conversion was achieved at a residence time of 8.5 s at 510 °C, and at around 5 s at 550 °C with the 1 wt% Ru/ZrO2 catalyst. The catalyst was not active enough to achieve complete gasification since high yields of primary products like acetic acid and acetaldehyde were still present. Carbon balances were between 80 and 60% in the catalytic experiments, decreasing continuously as the residence time was increased. This was attributed partially to the formation of methanol and acetaldehyde, which were not recovered and analyzed efficiently in our set-up, but also to the formation of carbon deposits. Carbon deposition was not observed on the catalyst particles but on the surface of the inert zirconia particles, especially at high residence time. This was related to the higher concentration of acetic acid and other acidic species in the catalytic experiments, which may polymerize to form tar-like carbon precursors. Because of carbon deposition, hydrogen yields were significantly lower than expected; for instance at 550 °C the hydrogen yield potential was only 50% of the stoichiometric value.
dc.format
25 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
University College London, Faculty of Mathematical and Physical Sciences, Department of Mathematics
dc.relation
Versió postprint del document publicat a: http://dx.doi.org/10.1016/j.cej.2010.04.005
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Chemical Engineering Journal, 2010, vol. 160, num. 2, p. 751-759
dc.relation
http://dx.doi.org/10.1016/j.cej.2010.04.005
dc.rights
(c) University College London, Faculty of Mathematical and Physical Sciences, Department of Mathematics, 2010
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Enginyeria Química i Química Analítica)
dc.subject
Biotecnologia
dc.subject
Gasificació de la biomassa
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Hidrogen
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Producció
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Ruteni
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Catalitzadors
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Biotechnology
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Biomass gasification
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Hydrogen
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Production
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Ruthenium
dc.subject
Catalysts
dc.title
Catalytic gasification of glycerol in supercritical water
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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