NIOBIUM OXIDE ACIDITY STUDIED BY PROTON BROAD-LINE NMR AT 4 K AND MASNMR AT ROOM-TEMPERATURE

Citation
P. Batamack et al., NIOBIUM OXIDE ACIDITY STUDIED BY PROTON BROAD-LINE NMR AT 4 K AND MASNMR AT ROOM-TEMPERATURE, Catalysis letters, 36(1-2), 1996, pp. 81-86
Citations number
27
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
1011372X
Volume
36
Issue
1-2
Year of publication
1996
Pages
81 - 86
Database
ISI
SICI code
1011-372X(1996)36:1-2<81:NOASBP>2.0.ZU;2-1
Abstract
The quantitative study of the Bronsted acidity of niobic acid (Nb2O5 . xH(2)O) using broad-line H-1 NMR at 4 K has been performed by interac ting niobic acid, pretreated at 573 K under vacuum, with water molecul es. The number of oxyprotonated species (H3O+, and H2O ... HO species formed, unreacted acidic OH groups or excess H2O molecules) deduced fr om the simulations of the broad-line H-1 NMR spectra shows a continuou s increase in the number of H3O+ species with adsorbed water molecules . This increase may be due to a classical dilution effect or to a syne rgistic interaction between Bronsted and Lewis acid sites. These resul ts are compared with those of some HY zeolites with or without framewo rk defects.