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dc.contributor.authorTabernilla, Zuria
dc.contributor.authorAteka Bilbao, Ainara
dc.contributor.authorBilbao Elorriaga, Javier
dc.contributor.authorAguayo Urquijo, Andrés Tomás ORCID
dc.contributor.authorEpelde Bejerano, Eva ORCID
dc.date.accessioned2024-10-25T12:57:20Z
dc.date.available2024-10-25T12:57:20Z
dc.date.issued2023-12
dc.identifier.citationEnergy 284 : (2023) // Article ID 128703es_ES
dc.identifier.issn1873-6785
dc.identifier.issn0360-5442
dc.identifier.urihttp://hdl.handle.net/10810/70187
dc.description.abstractEthylene oligomerization into liquid fuels at slightly over atmospheric pressure has been studied due to its interest to valorize online the excess of ethylene in sustainable olefins production processes and to intensify the production of fuel from refinery secondary streams. Runs were carried out in a fixed-bed reactor under the following conditions: 1.5 bar; 275–375 °C; space time, 2.7–16.2 gcatalyst h molC−1; time on stream, 5 h. The catalyst was prepared by agglomerating a HZSM-5 zeolite (SiO2/Al2O3 of 30) in a mesoporous matrix (γ-Al2O3/α-Al2O3). The hierarchical porous structure of the catalyst enables to reach a pseudo-steady state with a remarkable remnant activity after an initial deactivation period of 2–3 h. Temperature shows a relevant effect on ethylene conversion and product distribution, where a C5+ liquid fuel yield of 55% above 325 °C and 10.6 gcatalyst h molC−1 is obtained. At 325 °C, gasoline yield is 60%, with high olefin content (49%), which decreases at higher temperature, due to an increase in aromatic and paraffin concentration. Soft and hard coke analysis reveal the role of the matrix to attenuate deactivation. Moreover, above 325 °C the cracking of hard coke precursors deposited in the zeolite micropores prevails respect to their formation.es_ES
dc.description.sponsorshipThis work has been carried out with the financial support of the Ministry of Economy and Competitiveness of the Spanish Government (Project PID2022-140584OB-I00); the Basque Government (Project IT1645-22); and the European Regional Development Funds (ERDF) and the European Commission (HORIZON H2020-MSCA RISE 2018. Contract No. 823745). Z. Tabernilla is grateful for the PhD grant from the Department of Education, University and Research of the Basque Government (PRE_2022_2_0136). The authors thank for technical and human support provided by SGIker (UPV/EHU).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2022-140584OB-I00es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/823745es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectoligomerizationes_ES
dc.subjectethylenees_ES
dc.subjectHZSM-5 zeolitees_ES
dc.subjecthierarchical structurees_ES
dc.subjectfuelses_ES
dc.subjectcoke deactivationes_ES
dc.titlePerformance of HZSM-5 agglomerated in a mesoporous matrix in the fuel production from ethylene at atmospheric pressurees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND licensees_ES
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0360544223020972es_ES
dc.identifier.doi10.1016/j.energy.2023.128703
dc.contributor.funderEuropean Commission
dc.departamentoesIngeniería químicaes_ES
dc.departamentoeuIngeniaritza kimikoaes_ES


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© 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
Except where otherwise noted, this item's license is described as © 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license