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Low temperature catalytic oxidation of aldehydes using wood fly ash and molecular oxygen

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dc.contributor.author Kolar, P en
dc.contributor.author Kastner, JR en
dc.contributor.author Miller, J en
dc.date.accessioned 2014-06-06T06:47:25Z
dc.date.available 2014-06-06T06:47:25Z
dc.date.issued 2007 en
dc.identifier.issn 09263373 en
dc.identifier.uri http://dx.doi.org/10.1016/j.apcatb.2007.05.022 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/3584
dc.subject Activated carbon en
dc.subject Aldehydes en
dc.subject Catalytic autoxidation en
dc.subject Room temperature en
dc.subject Wood fly ash en
dc.subject.other Activated carbon en
dc.subject.other Catalyst activity en
dc.subject.other Fly ash en
dc.subject.other Low temperature effects en
dc.subject.other Molecular oxygen en
dc.subject.other Molecular weight en
dc.subject.other Oxidation en
dc.subject.other Solid wastes en
dc.subject.other Catalytic autoxidation en
dc.subject.other Room temperature en
dc.subject.other Wood fly ash en
dc.subject.other Aldehydes en
dc.title Low temperature catalytic oxidation of aldehydes using wood fly ash and molecular oxygen en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.apcatb.2007.05.022 en
heal.publicationDate 2007 en
heal.abstract Aldehydes, such a 2-methylbutanal (2-MB) and 3-methylbutanal (3-MB), are odorous and regulated VOCs generated in the poultry rendering process that are ineffectively removed in chemical wet scrubbers. It was theorized that wood fly ash or selective crystalline phases in the ash could act to catalyze the oxidation of aldehydes at room temperature in the presence of ClO2, resulting in a low-cost/energy air pollution control method. Results indicate that wood fly ash catalyzed the oxidation (i.e., breakdown) of 2-MB and 3-MB both in the presence of ClO2 and with just O2 (i.e., air) itself, potentially via a free radical mechanism. Aldehyde oxidation did not occur at measurable rates without the wood fly ash or activated carbon. The presence of ClO2 did not increase the rate, but altered the end products of oxidation. Wood fly ash also catalyzed the oxidation of 2-MB in the presence of air, leading to the appearance of 2-butanone, compared to acetone from 3-MB. Contact times of 30 s reduced 3-MB levels by ∼40% in bench scale, batch reactors. Similar results were found using activated charcoal (i.e., in terms of contact times), except that higher molecular weight compounds appeared to be formed. Continuous catalytic oxidation of 3-MB using wood fly ash was also demonstrated in a fixed-bed reactor at room temperature; the overall oxidation rate appeared to be first order with respect to 3-MB and a representative conversion of 20% at an inlet concentration of 67 ppmv and 2 s residence time (GHSV 1800 1/h, 25 °C, 1 atm) was measured. Results indicate the potential of using inexpensive solid waste materials to breakdown C5 aldehydes in rendering emissions to CO2, H2O, and less odor offensive compounds, but a carbon balance on the reaction and complete identification of end products are required for implementation. © 2007 Elsevier B.V. All rights reserved. en
heal.journalName Applied Catalysis B: Environmental en
dc.identifier.issue 3-4 en
dc.identifier.volume 76 en
dc.identifier.doi 10.1016/j.apcatb.2007.05.022 en
dc.identifier.spage 203 en
dc.identifier.epage 217 en


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