Adsorption and diffusion of n-hexane/2-methylpentane mixtures in zeolite silicalite: Experiments and modeling

Citation
D. Schuring et al., Adsorption and diffusion of n-hexane/2-methylpentane mixtures in zeolite silicalite: Experiments and modeling, J PHYS CH B, 105(32), 2001, pp. 7690-7698
Citations number
41
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
105
Issue
32
Year of publication
2001
Pages
7690 - 7698
Database
ISI
SICI code
1520-6106(20010816)105:32<7690:AADONM>2.0.ZU;2-7
Abstract
With the tracer-exchange positron emission profiling (TEX-PEP) technique, t he reexchange process of radioactively labeled molecules with a steady-stat e feed stream can be measured inside a zeolite-packed bed reactor. When the experimental tracer-exchange curves are modeled, values for the micropore diffusion and adsorption constant can be obtained. As one can choose which component to label, this technique is ideally suited for studying multicomp onent diffusion. In the present study, this technique has been used to meas ure the diffusive and adsorptive properties of an n-hexane/2-methylpentane mixture in zeolite silicalite. The measurements were performed at different ratios of n-hexane and 2-methylpentane in the gas phase at a constant tota l hydrocarbon pressure of 6.6 kPa and a temperature of 433 K. A slight pref erence for the adsorption of n-hexane was found because it is entropically more favorable to adsorb these molecules as they have no preferential sitin g in the zeolite pores; The diffusivity of the slowly moving 2-methylpentan e is not strongly affected by the presence of the fast moving n-hexane. The mobility of the linear alkane however strongly decreases with increasing 2 -methylpentane ratio and suddenly drops at a loading of approximately three 2-methylpentane molecules per unit cell. This is caused by the fact that t he branched alkanes are preferentially sited in the intersections between t he straight and zigzag channels of silicalite and therefore effectively blo ck the zeolite pore network. These results show that the adsorptive propert ies of the components and the structure of the zeolite network play an impo rtant role in the behavior of multicomponent mixtures in zeolites.