Low temperature CO adsorption on Na-ZSM-5 zeolites: An FTIR investigation

CO was adsorbed at 77 K on two Na-ZSM-5 zeolites which had Si/Al = 14 and Si/Al = 35, respectively. IR spectra in the OH-stretching region showed absorption bands at 3747 and 3673 cm −1 assigned, respectively, to terminal silanols and to hydroxyls located on extraframework aluminium species. These O...

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Veröffentlicht in:Journal of catalysis 1992-09, Vol.137 (1), p.179-185
Hauptverfasser: Bordiga, Silvia, Escalona Platero, Estrella, Otero Areán, Carlos, Lamberti, Carlo, Zecchina, Adriano
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Sprache:eng
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Zusammenfassung:CO was adsorbed at 77 K on two Na-ZSM-5 zeolites which had Si/Al = 14 and Si/Al = 35, respectively. IR spectra in the OH-stretching region showed absorption bands at 3747 and 3673 cm −1 assigned, respectively, to terminal silanols and to hydroxyls located on extraframework aluminium species. These OH groups were more strongly perturbed than silanols by adsorbed CO, thus suggesting a more pronounced Brønsted acidity. The major features of the spectra in the CO-stretching region are two intense absorptions centered, respectively, at 2178 and 2138 cm −1. Neither of them, however, is a single-peak band. The 2178-cm −1 band was assigned to CO molecules polarized by Na + ions. It could be resolved into two components, revealing coordination of Na + ions by one molecule (high-frequency component) or by more than one (low-frequency component). The high-frequency component showed an asymmetric profile which was assigned to the presence of Na + ions in slightly different environments. The 2138-cm −1 band corresponds to liquid-like CO inside the zeolite channels where the molecule behaves as a hindered rotor, thus explaining the fine structure observed. A weak IR absorption was also observed at 2112 cm −1 and assigned to CO simultaneously interacting through both ends with two Lewis acid centres. Finally, a combination mode observed at 2305–2315 cm −1 allowed assignation of a value of ca. 140 cm −1 to the Na +-CO stretching vibration.
ISSN:0021-9517
1090-2694
DOI:10.1016/0021-9517(92)90147-A