Adsorption of CO on NaZSM-5 zeolite under moderate temperature and pressure conditions: an FTIR investigation

Shete, B. S. ; Kamble, V. S. ; Gupta, N. M. ; Kartha, V. B. (1999) Adsorption of CO on NaZSM-5 zeolite under moderate temperature and pressure conditions: an FTIR investigation Physical Chemistry Chemical Physics, 1 (1). pp. 191-198. ISSN 1463-9076

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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/1999...

Related URL: http://dx.doi.org/10.1039/A807155A

Abstract

Adsorption of CO on NaZSM-5 zeolite was investigated at temperatures in the range 300-470 K and at pressures of 5-500 Torr using FTIR spectroscopy. The effect of exchanging the charge balancing cation in NaZSM-5 with a proton or calcium was evaluated. Data were also collected on NaY, CaY and CaX zeolites for comparison. We detected the development of six distinct CwO stretching bands with maxima at around 2111, 2130, 2146, 2160, 2176 and 2194 cm-1 during the adsorption of CO on NaZSM-5 zeolite at ambient temperatures. This was accompanied by the appearance of a prominent band at 2356 cm-1 and weak shoulder bands at frequencies around 2336, 2340, 2370 and 2380 cm-1 in the ν3 region of All the ν(CO) bands and CO2 . also the bands in the ν3 region of CO2 exhibited similar behaviour as a function of adsorbate pressure, evacuation, rise in sample temperature, and the exchange of charge balancing cation. For instance, the intensity of all the CwO stretching bands showed a similar growth behaviour with increasing adsorbate pressure, though the extent of this growth was di.erent for the individual IR bands. Similarly, these bands were removed simultaneously on evacuation. Furthermore, while all the vibrational bands in the v(CO) region showed a uniform isotopic shift corresponding to a frequency ratio ν(13C/12C) of ca. 0.977 and ν(18O/16O) of 0.976 for the adsorption of 13C16O and 12C18O, respectively, the bands in the ν3(CO2) region showed a red shift ?(13C/12C) of 0.972 with 13CO and an isotopic shift corresponding to 16O12C18O on 12C18O adsorption. No shift in ν(OH) bands was observed after CO adsorption under the conditions of this study. The results thus indicate that the individual zeolitic surface sites e.g., the Al3+ sites, Bronsted acid sites or the charge balancing cations, may not participate directly in the bonding of CO molecules at room temperature or above. Instead, the cage effect of zeolites plays an important role. The data are interpreted to suggest the formation of weakly bonded clusters of CO and CO2 molecules, occluded in the zeolitic cages and stabilized under the cationic field.

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