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dc.contributor.authorKu, Xiaoke
dc.contributor.authorLi, Tian
dc.contributor.authorLøvås, Terese
dc.date.accessioned2019-01-21T12:48:17Z
dc.date.available2019-01-21T12:48:17Z
dc.date.created2014-08-25T16:26:21Z
dc.date.issued2014
dc.identifier.citationEnergy & Fuels. 2014, 28 (8), 5184-5196.nb_NO
dc.identifier.issn0887-0624
dc.identifier.urihttp://hdl.handle.net/11250/2581555
dc.description.abstractIn this paper, a multiscale Eulerian–Lagrangian CFD model based on OpenFOAM has been constructed, which takes into account heat and mass transfer, pyrolysis, homogeneous and heterogeneous reactions, radiation, as well as the interactions between the continuous gas phase and discrete particles. The proposed model is validated and applied to a laboratory-scale biomass entrained-flow reactor. The operating temperatures are high (1000–1400 °C) and influences of five operating parameters (reactor temperature, steam/carbon molar ratio, excess air ratio, biomass type, and particle size) on the gasification behavior are explored. Results show that an increase in the reactor temperature has a positive effect on both the H2 and CO productions; increasing the steam/carbon ratio increases the H2 production but decreases the CO production; increasing the excess air ratio decreases both the H2 and CO productions; the variations in the gas product for the four biomasses studied are not so significant, because of similar biomass nature and, hence, one type can be replaced by another without any major consequences in the gasification performance; and both the CO and H2 productions and carbon conversion decrease with an increase in particle size. Moreover, the predicted results follow the same trend as the experimental data available in the literature. Quantitative comparisons are also made, and the agreement is good.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleEulerian–Lagrangian Simulation of Biomass Gasification Behavior in a High-Temperature Entrained-Flow Reactornb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber5184-5196nb_NO
dc.source.volume28nb_NO
dc.source.journalEnergy & Fuelsnb_NO
dc.source.issue8nb_NO
dc.identifier.doi10.1021/ef5010557
dc.identifier.cristin1149229
dc.relation.projectNorges forskningsråd: 193817nb_NO
dc.description.localcode© American Chemical Society 2014. This is the authors accepted and refereed manuscript to the article.nb_NO
cristin.unitcode194,64,25,0
cristin.unitnameInstitutt for energi- og prosessteknikk
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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