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dc.contributor.authorSelvaraj, M-
dc.contributor.authorLee, K-
dc.contributor.authorYoo, KS-
dc.contributor.authorLee, TG-
dc.date.accessioned2024-01-21T04:42:52Z-
dc.date.available2024-01-21T04:42:52Z-
dc.date.created2021-09-03-
dc.date.issued2005-06-06-
dc.identifier.issn1387-1811-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136367-
dc.description.abstractThe mesoporous molecular sieves Al-MCM-41 with Si/Al ratio equal to 16, was synthesized under hydrothermal conditions using cetyltrimethylammonium bromide (CTMA(+)Br(-)) as surfactant. The SO42-/Al-MCM-41(Si/Al = 16) material was synthesized using sulfuric acid under impregnation method, and the resulting material is sulfated Al-MCM-41 (SO42-/Al-MCM-41). The mesoporous materials viz. Al-MCM-41 and SO42-/Al-MCM-41 were characterized using several techniques e.g. ICP-AES, Nephelometer, XRD, FT-IR, TG/DTA, N-2-adsorption, solid-state-NMR, SEM, TEM and TPD-pyridine. By impregnating of sulfuric acid on silica surface, crystallinity, surface area, pore diameter and pore volume of SO42-/Al-MCM-41 decreased except wall thickness. While the Lewis acidity is increased because of the expelling aluminum from the Al-MCM-41 framework by impregnating sulfuric acid. The SO42-/Al-MCM-41 has been used for synthesis of 2-acetyl-6-methoxynaphthalene using 2-methoxynaphthalene with acetic anhydride as acylating agent and 1,2-dichloroethane as solvent. The catalytic results were compared with those obtained using 0.8 N sulfuric acid, amorphous silica-alumina, H-beta, USY and H-ZSM-5 zeolites. From the catalytic results it was concluded that the conversion of 2-methoxynaphthalene and selectivity of 2-acetyl-6-methoxynaphthalene in the S0(4)(2-)/Al-MCM-41 is higher than that in other catalysts due to higher number of Lewis acid sites. Thus the SO42-/Al-MCM-41 is found to be a highly active and recyclable heterogeneous catalyst while the catalyst is a very suitable for the synthesis of 2-acetyl-6-methoxynaphthalene. (c) 2005 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectFRIEDEL-CRAFTS ACYLATION-
dc.subjectACID-CATALYZED ACYLATION-
dc.subjectNAPHTHYL ETHER NEROLINE-
dc.subjectMCM-41/GAMMA-AL2O3 CATALYST-
dc.subjectZEOLITE-BETA-
dc.subjectHBEA ZEOLITE-
dc.subjectP-CYMENE-
dc.subjectMCM-41-
dc.subjectTOLUENE-
dc.subject2-METHOXYNAPHTHALENE-
dc.titleSynthesis of 2-acetyl-6-methoxynaphthalene using mesoporous SO42-/Al-MCM-41 molecular sieves-
dc.typeArticle-
dc.identifier.doi10.1016/j.micromeso.2005.02.017-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMICROPOROUS AND MESOPOROUS MATERIALS, v.81, no.1-3, pp.343 - 355-
dc.citation.titleMICROPOROUS AND MESOPOROUS MATERIALS-
dc.citation.volume81-
dc.citation.number1-3-
dc.citation.startPage343-
dc.citation.endPage355-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000229665200038-
dc.identifier.scopusid2-s2.0-18844442579-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusFRIEDEL-CRAFTS ACYLATION-
dc.subject.keywordPlusACID-CATALYZED ACYLATION-
dc.subject.keywordPlusNAPHTHYL ETHER NEROLINE-
dc.subject.keywordPlusMCM-41/GAMMA-AL2O3 CATALYST-
dc.subject.keywordPlusZEOLITE-BETA-
dc.subject.keywordPlusHBEA ZEOLITE-
dc.subject.keywordPlusP-CYMENE-
dc.subject.keywordPlusMCM-41-
dc.subject.keywordPlusTOLUENE-
dc.subject.keywordPlus2-METHOXYNAPHTHALENE-
dc.subject.keywordAuthorAl-MCM-41-
dc.subject.keywordAuthorSO42- /Al-MCM-41-
dc.subject.keywordAuthorLewis acidity-
dc.subject.keywordAuthorconversion of 2-methoxynaphthalene-
dc.subject.keywordAuthorselectivity of 2-acetyl-6-methoxynaphthalene-
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