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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17480
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dc.contributor.authorJacobs, P. A.-
dc.contributor.authorUytterhoeven, J. B.-
dc.date.accessioned2025-02-11T07:17:49Z-
dc.date.available2025-02-11T07:17:49Z-
dc.date.issued1973-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17480-
dc.description.abstractThe i.r. absorption curve of “ deep bed ” calcined NH4Y zeolites could be broken down into the same components as HY zeolites. The frequency of the peaks was slightly changed, but their half band width remained constant. In a scries of treatments representing increasing hydrolysis non-acidic OH bands around 3680 and 3600 cm-1 increase in intensity, due to surface OH groups near Al defect locations. Polynuclear Al species bridging the cubo-octahcdra are suggested to be partly responsible for the increased thermal stability. The non-acidic OH bands in synthetic faujasites exchanged with polyvalent cations are explained on the same basis, since they behave in a similar way as the non-acidic bands on “ deep bed ” zeolites after different treatments.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1973, 69 (2)en_US
dc.subjectChemistryen_US
dc.subjectHydroxyl Bandsen_US
dc.subjectInfrared Spectraen_US
dc.subjectZeolites X and Yen_US
dc.subjectPretreatment Effectsen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleAssignment of the Hydroxyl Bands in the Infrared Spectra of Zeolites X and Y: Part 2.—After Different Pretreatmentsen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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