Proton-loaded zeolites. 2. Dehydrohalogenation versus decationization kinetics: Cation and acidity effects


Ozin G. A., Özkar S., McMurray L.

Journal of Physical Chemistry, vol.94, no.21, pp.8289-8296, 1990 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 94 Issue: 21
  • Publication Date: 1990
  • Doi Number: 10.1021/j100384a054
  • Journal Name: Journal of Physical Chemistry
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.8289-8296
  • Ankara University Affiliated: No

Abstract

The work presented in part 1 of this study established that the sorption of anhydrous HX into dehydrated Na56Y progresses through a sequence of steps involving HX ionization and charge separation, oxygen framework protonation, formation of α-cage confined cation-anion contact ion pairs, and proton solvation by HX. A logical extension, which is the subject of this study, concerns the effect of extraframework alkali metal cation type (M = Li+, Na+, K+, Rb+, Cs+) on the sorption process. The question of the acidity of proton-loaded zeolites compared to Brønsted acid zeolites is addressed by using probe reactions with weak bases like ethane and cyclopropane. Additional insight into these systems is also obtained from a quantitative comparison of the kinetic and thermodynamic activation parameters for the dehydrohalogenation of proton-loaded zeolites exemplified by (HX)8Na56Y relative to the decationization (dehydroxylation) of Brønsted acid zeolites represented by H8Na48Y. © 1990 American Chemical Society.