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나노물질및화학반응연구단
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Mesoporous EU-1 zeolite as a highly active catalyst for ethylbenzene hydroisomerization

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dc.contributor.authorF. Marques Mota-
dc.contributor.authorP. Eliasova-
dc.contributor.authorJ. Jung-
dc.contributor.authorR. Ryoo-
dc.date.available2017-01-06T02:07:01Z-
dc.date.created2016-06-20-
dc.date.issued2016-04-
dc.identifier.issn2044-4753-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/3177-
dc.description.abstractThe hydroisomerization of ethylbenzene is an important industrial reaction to maximize the production of xylenes, and in particular, para-xylene. Zeolite EU-1 (with EUO topology) is commercially utilized in a physical mixture with a metallic phase (Pt/Al2O3). Herein, we have developed a micro-mesoporous EUO zeolite with a significant volume of intercrystalline mesoporosity to improve its catalytic performance in the industrial hydroisomerization of ethylbenzene. The use of a multivalent cationic surfactant as a capping agent was ideal to prevent uniform crystal growth and their aggregation, and to ensure the potential industrial applicability of the strategy. The corresponding mesoporosity and textural properties of nanosponge-like EUO were tuned according to the amount of the capping agent. The catalytic performance reflected the remarkable impact of a large exposed surface area (up to 55%) and a high amount of easily accessible Brønsted acid sites (up to 29%) in the EU-1 nanosponge on the catalytic yield. Our best catalyst revealed a three-fold increase in the conversion of ethylbenzene with no detrimental effects on the attained hydroisomerization yield. This approach presents a potential industrial capability in a wide range of catalytic applications as evidenced here in the hydroisomerization of ethylbenzene. © The Royal Society of Chemistry 2016-
dc.language영어-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleMesoporous EU-1 zeolite as a highly active catalyst for ethylbenzene hydroisomerization-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000374790200023-
dc.identifier.scopusid2-s2.0-84966262708-
dc.identifier.rimsid55861ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorF. Marques Mota-
dc.contributor.affiliatedAuthorP. Eliasova-
dc.contributor.affiliatedAuthorJ. Jung-
dc.contributor.affiliatedAuthorR. Ryoo-
dc.identifier.doi10.1039/c5cy02027a-
dc.identifier.bibliographicCitationCATALYSIS SCIENCE & TECHNOLOGY, v.6, no.8, pp.2735 - 2741-
dc.relation.isPartOfCATALYSIS SCIENCE & TECHNOLOGY-
dc.citation.titleCATALYSIS SCIENCE & TECHNOLOGY-
dc.citation.volume6-
dc.citation.number8-
dc.citation.startPage2735-
dc.citation.endPage2741-
dc.date.scptcdate2018-10-01-
dc.description.wostc4-
dc.description.scptc3-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for Nanomaterials and Chemical Reactions(나노물질 및 화학반응 연구단) > 1. Journal Papers (저널논문)
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Catal. Sci. Technol., 2016, 6, 2735–2741.pdfDownload

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