Adsorption of CHClF2 on a series of alkali metal (Li+, Na+, K+, Rb+, C
s+) ion-exchanged ZSM-5 zeolites have been studied by the analysis of
adsorption isotherms and IR spectroscopy. At low temperature (273 K),
physisorbed CHClF2 molecules filled up the pore of ZSM-5 zeolites wher
eas the isosteric heats of adsorption were much larger than the heat o
f condensation of CHClF2 irrespective of the cation incorporated in th
e zeolite. It was indicated, therefore, the adsorption in these system
s was governed by the dispersion force of pore wall. The microscopic c
haracter of admolecules was, however, strongly affected by the electri
c field of the cation. IR spectra of adsorbed CHClF2 indicated that th
e C-H bond of the admolecule was oriented in the parallel direction wi
th the electric field exerted by cation site, and these orientation re
sulted in a decrease in the intensity of nu(C-H) band and the low freq
uency shifts of nu(C-Cl) band. At high adsorption temperature (469 K),
surface analysis showed that a part of adsorbed CHClF2 reacted with A
l in the zeolite framework In a manner to form a surface compound cont
aining F and Al atoms.