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Catalytic ozonation of ammonia using biomass char and wood fly ash

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dc.contributor.author Kastner, JR en
dc.contributor.author Miller, J en
dc.contributor.author Kolar, P en
dc.contributor.author Das, KC en
dc.date.accessioned 2014-06-06T06:48:55Z
dc.date.available 2014-06-06T06:48:55Z
dc.date.issued 2009 en
dc.identifier.issn 00456535 en
dc.identifier.uri http://dx.doi.org/10.1016/j.chemosphere.2009.01.035 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/4336
dc.subject Ammonia en
dc.subject Biomass en
dc.subject Catalytic ozonation en
dc.subject Room temperature en
dc.subject Wood fly ash en
dc.subject.other Air streams en
dc.subject.other Biomass chars en
dc.subject.other Catalytic ozonation en
dc.subject.other Commercial catalysts en
dc.subject.other End products en
dc.subject.other Gaseous ammonias en
dc.subject.other Oxidation activities en
dc.subject.other Oxidation rates en
dc.subject.other Ozone concentrations en
dc.subject.other Power rates en
dc.subject.other Pseudo-zero-order kinetics en
dc.subject.other Residence time en
dc.subject.other Room temperature en
dc.subject.other Ammonia en
dc.subject.other Biological materials en
dc.subject.other Biomass en
dc.subject.other Catalysis en
dc.subject.other Catalysts en
dc.subject.other Fly ash en
dc.subject.other Industrial applications en
dc.subject.other Nitric oxide en
dc.subject.other Oxidation en
dc.subject.other Ozone en
dc.subject.other Ozone water treatment en
dc.subject.other Ozonization en
dc.subject.other Water vapor en
dc.subject.other Wood en
dc.subject.other Catalytic oxidation en
dc.subject.other ammonia en
dc.subject.other water en
dc.subject.other ammonia en
dc.subject.other biomass en
dc.subject.other catalyst en
dc.subject.other nitric oxide en
dc.subject.other oxidation en
dc.subject.other wood ash en
dc.subject.other article en
dc.subject.other biomass en
dc.subject.other catalysis en
dc.subject.other chemical reaction kinetics en
dc.subject.other fly ash en
dc.subject.other oxidation en
dc.subject.other ozonation en
dc.subject.other room temperature en
dc.subject.other water vapor en
dc.subject.other wood en
dc.subject.other Ammonia en
dc.subject.other Biomass en
dc.subject.other Carbon en
dc.subject.other Charcoal en
dc.subject.other Ozone en
dc.subject.other Particulate Matter en
dc.subject.other Temperature en
dc.subject.other Ammonia en
dc.subject.other Biomass en
dc.subject.other Catalysts en
dc.subject.other Fly Ash en
dc.subject.other Oxidation en
dc.subject.other Ozone en
dc.subject.other Temperature en
dc.subject.other Water Treatment en
dc.subject.other Water Vapor en
dc.subject.other Wood en
dc.title Catalytic ozonation of ammonia using biomass char and wood fly ash en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.chemosphere.2009.01.035 en
heal.publicationDate 2009 en
heal.abstract Catalytic ozonation of gaseous ammonia was investigated at room temperature using wood fly ash (WFA) and biomass char as catalysts. WFA gave the best results, removing ammonia (11 ppmv NH3, 45% conversion) at 23 °C at a residence time of 0.34 s, using 5 g of catalyst or ash at the lowest ozone concentration (62 ppmv). Assuming pseudo zero order kinetics in ozone, a power rate law of - rNH3 = 7.2 × 10- 8 CNH3 0.25 (r, mol g-1 s-1, CNH3 mol L-1) was determined at 510 ppmv O3 and 23 °C for WFA. Water vapor approximately doubled the oxidation rate using WFA and catalytic ozonation activity was not measured for the char without humidifying the air stream. Overall oxidation rates using the crude catalysts were lower than commercial catalysts, but the catalytic ozonation process operated at significantly lower temperatures (23 vs. 300 °C). Nitric oxide was not detected and the percentage of NO2 formed from NH3 oxidation ranged from 0.3% to 3% (v/v), with WFA resulting in the lowest NO2 level (at low O3 levels). However, we could not verify that N2O was not formed, so further research is needed to determine if N2 is the primary end-product. Additional research is required to develop techniques to enhance the oxidation activity and industrial application of the crude, but potentially inexpensive catalysts. © 2009 Elsevier Ltd. All rights reserved. en
heal.journalName Chemosphere en
dc.identifier.issue 6 en
dc.identifier.volume 75 en
dc.identifier.doi 10.1016/j.chemosphere.2009.01.035 en
dc.identifier.spage 739 en
dc.identifier.epage 744 en


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