A highly stable and selective Pt-modified mordenite catalyst for the skeletal isomerization of n-butane

José Ignacio Villegas, Narendra Kumar, Teemu Heikkilä, Agáta Smiešková, Pavol Hudec, Tapio Salmi, Dmitry Yu Murzin*

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

11 Citations (Scopus)

Abstract

The aim of this work is to investigate the skeletal isomerization of n-butane to isobutane over Pt-modified mordenite zeolite catalysts and proton form mordenite with different SiO2/Al2 O3 ratios. The 2-wt% Pt-H-MOR-20 and 2-wt% Pt-H-MOR-12.8 catalysts were synthesized by impregnation method, while H-MOR-12.8 and H-MOR-20 were obtained by calcinations of their ammonium-form counterparts. The influence of reaction temperature, carrier gas and dilution of the feed stream on the conversion of n-butane and yield of isobutane during time-on-stream has been studied. The Pt-modified mordenite catalysts have been characterized using XRD, scanning electron microscopy (SEM), nitrogen adsorption, CO chemisorption and FTIR of adsorbed pyridine. Pt-H-MOR-12.8 exhibited the highest yield and selectivity to isobutane and it was the most stable towards catalyst deactivation. Typically, an excess of propane with respect to pentanes was formed and the selectivity to pentanes remained constant for the different Pt-H-MOR and conditions tested. Selectivity to propane was inversely dependent on the H2 concentration in the feed and the SiO2 Al2O3 ratio.

Original languageEnglish
Pages (from-to)223-230
Number of pages8
JournalApplied Catalysis A: General
Volume284
Issue number1-2
DOIs
Publication statusPublished - 28 Apr 2005
MoE publication typeA1 Journal article-refereed

Keywords

  • Acidity
  • Isobutane
  • Mordenite
  • n-Butane
  • Platinum
  • Skeletal isomerization
  • Stability

Fingerprint Dive into the research topics of 'A highly stable and selective Pt-modified mordenite catalyst for the skeletal isomerization of n-butane'. Together they form a unique fingerprint.

Cite this