S. Ashtekar et al., FT-RAMAN STUDIES OF SINGLE-COMPONENT AND BINARY ADSORPTION IN SILICALITE-1, Journal of the Chemical Society. Faraday transactions, 94(8), 1998, pp. 1157-1161
Citations number
28
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
FT-Raman spectroscopy has been used to probe single-component and bina
ry-component adsorption of benzene, p-xylene and cyclohexane in silica
lite-1. It was shown that FT-Raman is not only able to probe the sorba
te-framework interaction related to the phase transitions commonly obs
erved when organic species are sorbed within silicalite-1, but also pr
ovides a sensitive and direct probe of sorbate-sorbate interactions wi
thin the zeolite framework. Single-component adsorption of benzene, p-
xylene and cyclohexane in silicalite-1 has been considered at various
loadings. In the case of benzene adsorption, FT-Raman spectroscopy was
shown to detect the transformation in sorbate interactions associated
with the transformation in crystal symmetry from monoclinic P2(1)/n.1
.1 to orthorhombic Pnma at a sorbate loading of 4 molecules per unit c
ell. We also confirmed the results of Huang (J. Am. Chem. Sec., 1996,
118, 7233) in detecting the sorbate-induced crystal-phase transition f
rom orthorhombic Pnma to orthorhombic P2(1)2(1)2(1) for the case of p-
xylene adsorption at loadings in excess of 4 molecules per unit cell.
No evidence of a crystal-phase transition as a function of sorbate loa
ding was observed for the case of cyclohexane adsorption, consistent w
ith earlier studies. It was shown that, in the case of benzene-p-xylen
e co-adsorption, benzene and p-xylene access the sites most favoured d
uring the respective single-component adsorption processes. In contras
t, cyclohexane when co-adsorbed with either benzene or p-xylene was se
en to compete for the same sites, forcing benzene and p-xylene into le
ss favoured adsorption sites.