dc.contributor.author | Crespo Briones, Iratxe | |
dc.contributor.author | Palos Urrutia, Roberto | |
dc.contributor.author | Trueba Fraile, Juan David | |
dc.contributor.author | Bilbao Elorriaga, Javier | |
dc.contributor.author | Arandes Esteban, José María | |
dc.contributor.author | Gutiérrez Lorenzo, Alazne | |
dc.date.accessioned | 2024-05-24T15:06:41Z | |
dc.date.available | 2024-05-24T15:06:41Z | |
dc.date.issued | 2023-02 | |
dc.identifier.citation | Fuel 334(Part 1) : (2023) // Article ID 126579 | es_ES |
dc.identifier.issn | 0016-2361 | |
dc.identifier.issn | 1873-7153 | |
dc.identifier.uri | http://hdl.handle.net/10810/68161 | |
dc.description.abstract | Motivated by the necessity of intensifying the valorization of secondary refinery streams and of extending the life cycle of the catalysts, this study aims to obtain high quality gasoline in the hydrocracking of a pre-hydrotreated light cycle oil (HT-LCO) using noble metals catalysts supported on a spent fluid catalytic cracking (FCC) catalyst. Hydrocracking runs have been carried out in a fixed bed reactor with two different catalysts (Pt/FCC and Pd/FCC) under the following conditions: 320–400 °C; 80 bar; hydrogen to HT-LCO ratio, 1000 NmL mL−1; weight hourly space velocity (WHSV), 4.48 h−1; and time on stream (TOS), 8 h. The results have exposed that 400 °C is the optimal temperature for hydrocracking the HT-LCO, since the yield of gasoline is clearly maximized (yielding up to 80 wt%) at the same time that the formation of gases is minimized. Comparing both catalysts, the Pt/FCC catalyst has offered better performance as its high hydrogenation capacity has allowed for obtaining an isoparaffinic gasoline fraction with a RON of 93.0. These good results lay on two facts that avoid the blocking of the micropores of the zeolite HY by the deposition of coke: (i) the hydrocracking of the coke precursors; and (ii) the matrix of the FCC catalyst where a fraction of the coke is deposited. In this way, after an initial deactivation period, the catalysts have reached a pseudo-stable state with a notorious remaining catalytic activity (higher for the Pt/FCC catalyst). | es_ES |
dc.description.sponsorship | his work has been carried out with the financial support of the Ministry of Science and Innovation of the Spanish Government (grant PID2021-125255OB-I00), the European Union’s ERDF funds and Horizon 2020 research and innovation program under the Marie Skłodowska-Curie Actions (grant No 823745) and the Basque Government (grant IT1645-22). Iratxe Crespo and David Trueba thank the University of the Basque Country UPV/EHU for their PhD grants (PIF 2021 and PIF 2018, respectively).
The authors thank for technical and human support provided by SGIker of UPV/EHU and European funding (ERDF and ESF). The authors also acknowledge Petronor refinery for providing the feed and the FCC catalyst used in the work. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Elsevier | es_ES |
dc.relation | info:eu-repo/grantAgreement/EC/H2020/823745 | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/PID2021-125255OB-I00 | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/es/ | * |
dc.subject | LCO | es_ES |
dc.subject | hydrocracking | es_ES |
dc.subject | FCC catalyst | es_ES |
dc.subject | deactivation | es_ES |
dc.subject | gasoline | es_ES |
dc.title | Intensifying gasoline production in the hydrocracking of pre-hydrotreated light cycle oil by means of Pt and Pd supported on a spent FCC catalyst | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | © 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-
nc/4.0/) | es_ES |
dc.rights.holder | Atribución-NoComercial 3.0 España | * |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0016236122034032 | es_ES |
dc.identifier.doi | 10.1016/j.fuel.2022.126579 | |
dc.contributor.funder | European Commission | |
dc.departamentoes | Ingeniería química | es_ES |
dc.departamentoeu | Ingeniaritza kimikoa | es_ES |