Pt/SAPO-5 and Pt/SAPO-11 as catalysts for the hydroisomerization and hydrocracking of n-octane
- 1 January 1995
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Faraday Transactions
- Vol. 91 (10) , 1551-1555
- https://doi.org/10.1039/ft9959101551
Abstract
n-Octane hydroisomerization and hydrocracking on SAPO-5 and SAPO-11 catalysts containing 0.5 wt.% Pt have been investigated in a flow reactor over a wide range of temperatures (573–708 K) and pressures (atmospheric, 3 and 5 bar). These studies have shown that hydroisomerization is a function of the total conversion. The primary products obtained with n-octane were the monobranched isomers. Multibranched feed isomers and cracked products were formed in subsequent reactions. In all cases, hydrogen pressure had a strong influence on the activity and time-on-stream deactivation. Hydroisomerization can be considered to be the primary reaction, with hydrocracking occurring to a significant extent only at higher conversions ( > 40% for Pt/SAPO-5 and > 65% for Pt/SAPO-11). The selectivity patterns found in these molecular-sieve catalysts are interpreted in terms of a series of reaction pathways incorporating both confinement effects and shape selectivity factors.This publication has 3 references indexed in Scilit:
- Selectivities in methylcyclopentane and n-hexane conversion on some metal-loaded SAPO-11 catalystsApplied Catalysis A: General, 1992
- Kinetics of the hydroisomerization and hydrocracking of paraffins on a platinum containing bifunctional Y-zeoliteCatalysis Today, 1987
- Electrophilic Substitutions at Alkanes and in Alkylcarbonium IonsPublished by Wiley ,1972