NH3 AS A PROBE MOLECULE FOR NMR AND IR STUDY OF ZEOLITE CATALYST ACIDITY

Citation
F. Yin et al., NH3 AS A PROBE MOLECULE FOR NMR AND IR STUDY OF ZEOLITE CATALYST ACIDITY, JOURNAL OF PHYSICAL CHEMISTRY B, 101(10), 1997, pp. 1824-1830
Citations number
37
Categorie Soggetti
Chemistry Physical
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
101
Issue
10
Year of publication
1997
Pages
1824 - 1830
Database
ISI
SICI code
1089-5647(1997)101:10<1824:NAAPMF>2.0.ZU;2-2
Abstract
The measurement of the numbers of Bronsted and Lewis acid sites has be en performed quantitatively using NH3 as an infrared molecular probe. The assignment of the deformation NH4+ and NH3 bands has been carried out by comparing the proton MAS NMR spectra with the corresponding inf rared spectra in dealuminated acid ZSM-5 (DHZ). It has been shown that the total number of Bronsted sites is equal to the number of OH bridg ing a silicon to an aluminum in a (4)Q(1A1) cluster. This represents a variable fraction of the content in framework aluminum (FA1), dependi ng on the zeolite composition. The bridging OH in (4)Q(nAI), n > 1, cl usters are not Bronsted sites, in agreement with the results of a rece nt REDOR study. The number of Lewis sites (L:NH3) is a fraction of the nonframework aluminum content (NFAl). The Lewis sites dispersion rati o L:NH3/NFAl is between 75 and 40%, depending upon the temperature (11 5 or 175 degrees C) used for outgassing the sample after NH3 adsorptio n. The quantitative results obtained with NH3 IR are compared to the q ualitative results obtained earlier by low-temperature CO IR. This com parison shows that, in DHZ as well as in USY, two types of Bronsted si tes exist. The strongest Bronsted sites are related to FAl1, a computa ble number representing a bridging OH in a (4)Q(1Al) environment with no next-nearest-neighbor aluminum.