ISOMERIZATION AND HYDROCRACKING OF HEPTANE OVER BIMETALLIC BIFUNCTIONAL PTPD H-BETA AND PTPD/USY ZEOLITE CATALYSTS/

Citation
E. Blomsma et al., ISOMERIZATION AND HYDROCRACKING OF HEPTANE OVER BIMETALLIC BIFUNCTIONAL PTPD H-BETA AND PTPD/USY ZEOLITE CATALYSTS/, Journal of catalysis, 165(2), 1997, pp. 241-248
Citations number
33
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
00219517
Volume
165
Issue
2
Year of publication
1997
Pages
241 - 248
Database
ISI
SICI code
0021-9517(1997)165:2<241:IAHOHO>2.0.ZU;2-Y
Abstract
Bifunctional catalysts are prepared by loading NH4-Beta zeolites with platinum, palladium, and platinum-palladium metal combinations via cat ion exchange and incipient wetness impregnation with Pt(NH3)(4)Cl-2 an d Pd(NH3)(4)Cl-2 complexes, followed by calcination and reduction. In comparison to the Pt and Pd loaded acid zeolites, the bimetallic Pd-Pt zeolites are found to be more active and selective in the isomerizati on of heptane. The noble metal phases are characterized with temperatu re programmed reduction and hydrogen chemisorption. The dispersion of platinum is significantly improved in presence of as little as 20 mole % of palladium. The improved Pt dispersion leads to a better intimacy and balance of the acid and hydrogenation-dehydrogenation functions in these bifunctional catalysts and suppression of undesirable hydrogeno lysis and dimerization-cracking activity. On Pt/USY zeolite, the addit ion of palladium has similar beneficial effects on the catalytic perfo rmances. (C) 1997 Academic Press