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dc.contributor.authorVela Díaz, Francisco Javier
dc.contributor.authorPalos Urrutia, Roberto
dc.contributor.authorRodríguez Plaza, Suní
dc.contributor.authorAzkoiti Elustondo, Miren Josune
dc.contributor.authorBilbao Elorriaga, Javier
dc.contributor.authorGutiérrez Lorenzo, Alazne ORCID
dc.date.accessioned2023-06-22T17:37:54Z
dc.date.available2023-06-22T17:37:54Z
dc.date.issued2023-03
dc.identifier.citationJournal of Analytical and Applied Pyrolysis 170 : (2023) // Article ID 105928es_ES
dc.identifier.issn0165-2370
dc.identifier.issn1873-250X
dc.identifier.urihttp://hdl.handle.net/10810/61567
dc.description.abstractPursuing the aim of improving the current waste plastics management strategy, we have investigated the co-hydrocracking of high-density polyethylene (HDPE) with vacuum gasoil (VGO) over a PtPd/HY catalyst for converting this blend into high-quality fuels. In particular, the work was focused on assessing the effects of the reaction time on the product yields and on the composition of the gas, naphtha and light cycle oil (LCO) fractions, which was determined by chromatographic means. The experimental runs were carried out in a 100 mL semi continuous stirred tank reactor varying the reaction time between 15 and 120 min and maintaining constant the rest of the variables at 420 °C (temperature reached using an electrical heating jacket and following a 5 °C min−1 heating ramp), 80 bar and a catalyst to oil mass ratio of 0.075 gcat goil−1. The results shown that at 120 min a naphtha fraction rich in 1-ring aromatics and with a RON value of 92.5 was obtained, while the LCO fraction was mainly iso-paraffinic with a cetane index of 43.8. Hence, these fractions could be used in the corresponding blending stages of commercial gasoline and diesel. Furthermore, the coke deposited on the catalyst was analyzed by means of TPO, obtaining that it was mainly formed at short contact times (< 15 min) and that its nature evolved with contact time being less condensed at long contact times.es_ES
dc.description.sponsorshipThis work has been carried out with the following financial support: (i) grant PID2021–125255OB-I00 funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”; (ii) the European Union’s Horizon 2020 Research and Innovation Program under the Marie Skłodowska-Curie Actions (grant No 823745); and, (iii) the Basque Government (grant IT1645-22).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/823745es_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2021–125255OB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjecthydrocrackinges_ES
dc.subjectplastices_ES
dc.subjectvacuum gasoiles_ES
dc.subjectwaste refineryes_ES
dc.subjectfueles_ES
dc.titleStudy on the role of the reaction time in the upcycling of HDPE by co-hydrocracking it with VGOes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/)es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0165237023000724es_ES
dc.identifier.doi10.1016/j.jaap.2023.105928
dc.contributor.funderEuropean Commission
dc.departamentoesIngeniería químicaes_ES
dc.departamentoesIngeniería química y del medio ambientees_ES
dc.departamentoeuIngeniaritza kimikoaes_ES
dc.departamentoeuIngeniaritza kimikoa eta ingurumenaren ingeniaritzaes_ES


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© 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-
nc-nd/4.0/)
Except where otherwise noted, this item's license is described as © 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/)