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dc.contributor.authorNetzer, Corinna
dc.contributor.authorLi, Tian
dc.contributor.authorSeidel, Lars
dc.contributor.authorMauss, Fabian
dc.contributor.authorLøvås, Terese
dc.date.accessioned2020-12-02T09:11:10Z
dc.date.available2020-12-02T09:11:10Z
dc.date.created2020-11-27T15:32:32Z
dc.date.issued2020
dc.identifier.issn0887-0624
dc.identifier.urihttps://hdl.handle.net/11250/2711353
dc.description.abstractBiomass devolatilization and incineration in grate-fired plants are characterized by heterogeneous fuel mixtures, often incompletely mixed, dynamical processes in the fuel bed and on the particle scale, as well as heterogeneous and homogeneous chemistry. This makes modeling using detailed kinetics favorable but computationally expensive. Therefore, a computationally efficient model based on zero-dimensional stochastic reactors and reduced chemistry schemes, consisting of 83 gas-phase species and 18 species for surface reactions, is developed. Each reactor is enabled to account for the three phases: the solid phase, pore gas surrounding the solid, and the bulk gas. The stochastic reactors are connected to build a reactor network that represents the fuel bed in grate-fired furnaces. The use of stochastic reactors allows us to account for incompletely mixed fuel feeds, distributions of local temperature and local equivalence ratio within each reactor and the fuel bed. This allows us to predict the released gases and emission precursors more accurately than if a homogeneous reactor network approach was employed. The model approach is demonstrated by predicting pyrolysis conditions and two fuel beds of grate-fired plants from the literature. The developed approach can predict global operating parameters, such as the fuel bed length, species release to the freeboard, and species distributions within the fuel bed to a high degree of accuracy when compared to experiments.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.titleStochastic Reactor-Based Fuel Bed Model for Grate Furnacesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionacceptedVersionen_US
dc.source.journalEnergy & Fuelsen_US
dc.identifier.doi10.1021/acs.energyfuels.0c02868
dc.identifier.cristin1853481
dc.relation.projectNorges forskningsråd: 267957en_US
dc.description.localcodeLocked until 12.11.2021 due to copyright restrictions. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Energy & Fuels, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see DOI: 10.1021/acs.energyfuels.0c02868en_US
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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