disproportionation and isomerization relative to the n-olefin case which together with the lower rate of aromatization is due to greater deactivation.It is well known that coke enhances the p-selectivity of ZSM-5 (Kaeding et al. 1981), p-alkylaromatics having a greater diffusivity than their 0-and m-counterparts, so by eliminating the surface acid sites, the product becomes increasingly p-selective. Thus it is likely that the m-+ pxylene product from 2-methylpropene is predominantly pxylene. Upon adsorption on a Bronsted acid site, the 2-methylpropene forms an isobutyl cation, the tertiary carbenium ion being more stable than the secondary one formed in n-olefin adsorption. van den Berg et al. (1983) have reported that isobutyl carbenium ions form readily on the weakly acidic external acid sites of ZSM-5 and lead to coke formation resulting in pore mouth blockage. The results in Table 2 support pore mouth blockage as the yield decreases more rapidly with time on stream for toluene and the xylenes than for benzene.It follows, then, that for successful upgrading of offgas streams to a BTX product, the amount of iso-olefins in the feed should be kept to a minimum, otherwise the higher coking rates will result in a concomitant loss in activity.
Acknowledgements
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