File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

박영빈

Park, Young-Bin
Functional Intelligent Materials Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.startPage 111893 -
dc.citation.title MICROPOROUS AND MESOPOROUS MATERIALS -
dc.citation.volume 336 -
dc.contributor.author Biswas, Subir -
dc.contributor.author Baruah, Manash J. -
dc.contributor.author Gogoi, Gautam -
dc.contributor.author Hoque, Nazimul -
dc.contributor.author Lee, Seonghwan -
dc.contributor.author Park, Young-Bin -
dc.contributor.author Saikia, Lakshi -
dc.contributor.author Bania, Kusum K. -
dc.date.accessioned 2023-12-21T14:11:23Z -
dc.date.available 2023-12-21T14:11:23Z -
dc.date.created 2022-05-31 -
dc.date.issued 2022-05 -
dc.description.abstract An economically viable approach for the synthesis of different alpha, 8-unsaturated aldehydes through modified cross-aldol condensation reaction has been developed. In this synthetic process, acetaldehyde is generated in situ through the catalytic dehydrogenation of the ethanol. The dehydrogenation reaction is found to occur over copper oxide nanoparticles supported on magnesium exchanged zeolite-Y. The formation of acetaldehyde through dehydrogenation of ethanol is confirmed by the modified Hantzsch reaction. Different kinetic studies have been performed to predict the rate of acetaldehyde as well as cinnamaldehyde formation. The formation of alpha, 8-unsaturated aldehydes through the dehydrogenative cross-aldol reaction of ethanol with various aldehydes are found to be dependent on different reaction parameters viz temperature, catalyst amount, time, and the nature of bases. The catalytic dehydrogenation process is found to occur within 80-100 C. TDDFT calculations are used to correlate the electronic spectra of Hantzsch reaction product with the experimental one. -
dc.identifier.bibliographicCitation MICROPOROUS AND MESOPOROUS MATERIALS, v.336, pp.111893 -
dc.identifier.doi 10.1016/j.micromeso.2022.111893 -
dc.identifier.issn 1387-1811 -
dc.identifier.scopusid 2-s2.0-85127811642 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/58645 -
dc.identifier.url https://www.sciencedirect.com/science/article/pii/S1387181122002116?via%3Dihub -
dc.identifier.wosid 000793654600003 -
dc.language 영어 -
dc.publisher ELSEVIER -
dc.title Dehydrogenation of ethanol over CuO-Mg-Y for cross-aldol condensation with aryl aldehydes -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Applied; Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Science & Technology - Other Topics; Materials Science -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor CuO-Mg-Y -
dc.subject.keywordAuthor Ethanol dehydrogenation -
dc.subject.keywordAuthor Cross-aldol reaction -
dc.subject.keywordAuthor Cinnamaldehyde -
dc.subject.keywordPlus COPPER-OXIDE NANOPARTICLES -
dc.subject.keywordPlus DENSITY-FUNCTIONAL THEORY -
dc.subject.keywordPlus EXCITATION-ENERGIES -
dc.subject.keywordPlus GEOMETRIC DERIVATIVES -
dc.subject.keywordPlus SELECTIVE OXIDATION -
dc.subject.keywordPlus ACTIVE-SITES -
dc.subject.keywordPlus CATALYSTS -
dc.subject.keywordPlus METHANOL -
dc.subject.keywordPlus QUANTIFICATION -
dc.subject.keywordPlus RESONANCE -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.