Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/28477
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dc.contributor.authorGanjala, Venkata Siva Prasad-
dc.contributor.authorMutyala, Suresh-
dc.contributor.authorNeeli, Chinna Krishna Prasad-
dc.contributor.authorKhagga, Mukkanti-
dc.contributor.authorRao, Kamaraju Seetha Rama-
dc.contributor.authorBurri, David Raju-
dc.date.accessioned2014-04-19T12:31:44Z-
dc.date.available2014-04-19T12:31:44Z-
dc.date.issued2014-04-19T12:31:44Z-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/28477-
dc.description545-549en_US
dc.description.abstractA series of triflamide anchored SBA-15 (SBA-NH-TA) catalysts with 5-20 wt% triflic acid (TA) loadings have been synthesized through the functionalization of propylamine on the surface of SBA-15 (SBA-NH2), followed by covalent attachment of triflic acid with –NH2 group of SBA-NH2. With SBA-NH-TA as catalyst and 69% HNO3 as nitrating agent, highly accelerated and safe nitration of aromatic compounds in microwave under solvent-free conditions has been achieved. The structural and textural characteristics of SBA-NH-TA catalysts have been determined from N2 sorption and low-angle XRD techniques. As the loading of TA increases, the conversion of alkylaromatics to their nitrated products increases significantly. Reaction parameters like amount of catalyst, amount of triflic acid loading, substrate to nitric acid ratio, reaction temperature and reaction time have been investigated. en_US
dc.language.isoen_USen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.53A(04-05) [April-May 2014]en_US
dc.subjectCatalystsen_US
dc.subjectNitrationen_US
dc.subjectMetal-free nitrationen_US
dc.subjectTriflamide anchored SBA-15en_US
dc.subjectAlkyl aromaticsen_US
dc.subjectXyleneen_US
dc.titleTriflamide anchored SBA-15 catalyst for nitration of alkyl aromatics in microwaveen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.53A(04-05) [April-May 2014]

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