Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/409
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRani, P.-
dc.contributor.authorSrivastava, R.-
dc.contributor.authorBiswarup, S.-
dc.date.accessioned2016-11-18T05:38:10Z-
dc.date.available2016-11-18T05:38:10Z-
dc.date.issued2016-11-17-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/409-
dc.description.abstractA novel, dual template mediated, one-step direct synthesis route is reported here for the preparation of nanocrystalline zeolites of different framework structures (such as ZSM-5, mordenite, and sodalite). In this synthesis strategy, a suitably designed dicationic/tetra-cationic soft template was used along with a conventional zeolite structure director to obtain nanocrystalline zeolites with nanosheet morphology. Nanocrystalline zeolites exhibited large surface area, pore volume, and intercrystalline mesopores. The long hydrophobic chain containing a multiammonium template cooperatively participates in the zeolite crystallization process along with a conventional microporous zeolite structure director to form the ultrathin microporous zeolite framework, while the hydrophobic interaction between the long chains restricted the excessive growth of zeolites and induced the formation of intercrystalline mesopores. Nanocrystalline zeolites exhibited exceptionally high activity in the acid-catalyzed reactions involving large molecules when compared with conventional zeolites. This synthesis strategy can be extended for the preparation of zeolites of different framework structures or other porous materials in the future.en_US
dc.language.isoen_USen_US
dc.titleOne-step dual template mediated synthesis of nanocrystalline zeolites of different framework structuresen_US
dc.typeArticleen_US
Appears in Collections:Year-2016

Files in This Item:
File Description SizeFormat 
Full Text.pdf8.55 MBAdobe PDFView/Open    Request a copy


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