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dc.contributor.authorMei, Danhua
dc.contributor.authorLiu, Shiyun
dc.contributor.authorYanik, Jale
dc.contributor.authorLópez Zabalbeitia, Gartzen ORCID
dc.contributor.authorOlazar Aurrecoechea, Martin
dc.contributor.authorFang, Zhi
dc.contributor.authorTu, Xin
dc.date.accessioned2022-09-07T10:35:42Z
dc.date.available2022-09-07T10:35:42Z
dc.date.issued2022
dc.identifier.citationACS Sustainable Chemistry & Engineering 10(27) : 8958-8969 (2022)es_ES
dc.identifier.issn2168-0485
dc.identifier.urihttp://hdl.handle.net/10810/57458
dc.description.abstract[EN] Biomass gasification is a promising and sustainable process to produce renewable and CO2-neutral syngas (H2 and CO). However, the contamination of syngas with tar is one of the major challenges to limit the deployment of biomass gasification on a commercial scale. Here, we propose a hybrid plasma-catalytic system for steam reforming of tar compounds over honeycombbased catalysts in a gliding arc discharge (GAD) reactor. The reaction performances were evaluated using the blank substrate and coated catalytic materials (gamma-Al2O3 and Ni/gamma-Al2O3). Compared with the plasma alone process, introducing the honeycomb materials in GAD prolonged the residence time of reactant molecules for collision with plasma reactive species to promote their conversions. The presence of Ni/gamma-Al2O3 gave the best performance with the high conversion of toluene (86.3%) and naphthalene (75.5%) and yield of H2 (35.0%) and CO (49.1%), while greatly inhibiting the formation of byproducts. The corresponding highest overall energy efficiency of 50.9 g/kWh was achieved, which was 35.4% higher than that in the plasma alone process. Characterization of the used catalyst and long-term running indicated that the honeycomb material coated with Ni/gamma-Al2O3 had strong carbon resistance and excellent stability. The superior catalytic performance of Ni/gamma-Al2O3 can be mainly ascribed to the large specific surface area and the in situ reduction of nickel oxide species in the reaction process, which promoted the interaction between plasma reactive species and catalysts and generated the plasma-catalysis synergy.es_ES
dc.description.sponsorshipThe support of this work by the National Natural Science Foundation of China (no. 51907087), the Natural Science Foundation of Jiangsu Province (no. BK20190675), the Postdoctoral Science Foundation of China (no. 2020M671289), and the Natural Science Foundation for Colleges in Jiangsu Province (no. 19KJB470005) is gratefully acknowledged. The authors acknowledge the funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement (no. 823745). X.T. thanks the support of the Royal Society Newton Advanced Fellowship (NAF/R1180230) and the British Council (No. 623389161). J.Y. acknowledges funding from the Scientific and Technological Research Council of Turkey (TUBITAK Project Contract No. 219M123).es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/823745es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectgliding arces_ES
dc.subjecthoneycomb catalystes_ES
dc.subjectbiomass gasificationes_ES
dc.subjecttar reforminges_ES
dc.subjectplasma catalysises_ES
dc.titlePlasma-Catalytic Reforming of Naphthalene and Toluene as Biomass Tar over Honeycomb Catalysts in a Gliding Arc Reactores_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 The Authors. Published by American Chemical Society. Attribution 4.0 International (CC BY 4.0)es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acssuschemeng.2c02495es_ES
dc.identifier.doi10.1021/acssuschemeng.2c02495
dc.contributor.funderEuropean Commission
dc.departamentoesIngeniería químicaes_ES
dc.departamentoeuIngeniaritza kimikoaes_ES


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© 2022 The Authors. Published by American Chemical Society.
Attribution 4.0 International (CC BY 4.0)
Except where otherwise noted, this item's license is described as © 2022 The Authors. Published by American Chemical Society. Attribution 4.0 International (CC BY 4.0)