Mesoporous EU-1 zeolite as a highly active catalyst for ethylbenzene hydroisomerization
DC Field | Value | Language |
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dc.contributor.author | F. Marques Mota | - |
dc.contributor.author | P. Eliasova | - |
dc.contributor.author | J. Jung | - |
dc.contributor.author | R. Ryoo | - |
dc.date.available | 2017-01-06T02:07:01Z | - |
dc.date.created | 2016-06-20 | - |
dc.date.issued | 2016-04 | - |
dc.identifier.issn | 2044-4753 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/3177 | - |
dc.description.abstract | The 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.language | 영어 | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.title | Mesoporous EU-1 zeolite as a highly active catalyst for ethylbenzene hydroisomerization | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000374790200023 | - |
dc.identifier.scopusid | 2-s2.0-84966262708 | - |
dc.identifier.rimsid | 55861 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | F. Marques Mota | - |
dc.contributor.affiliatedAuthor | P. Eliasova | - |
dc.contributor.affiliatedAuthor | J. Jung | - |
dc.contributor.affiliatedAuthor | R. Ryoo | - |
dc.identifier.doi | 10.1039/c5cy02027a | - |
dc.identifier.bibliographicCitation | CATALYSIS SCIENCE & TECHNOLOGY, v.6, no.8, pp.2735 - 2741 | - |
dc.relation.isPartOf | CATALYSIS SCIENCE & TECHNOLOGY | - |
dc.citation.title | CATALYSIS SCIENCE & TECHNOLOGY | - |
dc.citation.volume | 6 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 2735 | - |
dc.citation.endPage | 2741 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 4 | - |
dc.description.scptc | 3 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |