Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Pt/Al{sub 2}O{sub 3} catalysts and Pt-Sn/Al{sub 2}O{sub 3} catalysts prepared by two different methods: Hydrogen pressure effects in the reactions of n-hexane

Journal Article · · Journal of Catalysis
; ;  [1]
  1. Institute of Isotopes of the Hungarian Academy of Sciences, Budapest (Hungary); and others

Pt-Sn/Al{sub 2}O{sub 3} catalysts were prepared using two different methods, namely, by {open_quotes}traditional{close_quotes} coimpregnation with H{sub 2}PtCl{sub 6} and SnCl{sub 4} and by a {open_quotes}new{close_quotes} method in which the bimetallic complex precursor [Pt(NH{sub 3}){sub 4}] [SnCl{sub 6}] is prepared on the support. Their catalytic activity and selectivity in n-hexane reactions were studied as a function of the hydrogen pressure (60-480 Torr) and compared with those of monometallic Pt/Al{sub 2}O{sub 3} catalysts using H{sub 2}PtCl{sub 6} or [Pt(NH{sub 3}){sub 4}]Cl{sub 2} as Pt precursors. Pt/Al{sub 2}O{sub 3} ex [Pt(NH{sub 3}){sub 4}]Cl{sub 2} showed very low dispersion and exhibited high selectivity in reactions attributed to multiatomic ensembles. The results with bimetallic catalysts can be rationalized in terms of two phases being present, a PtSn alloy phase plus Pt in fine distribution. The {open_quotes}new{close_quotes} Pt-Sn/Al{sub 2}O{sub 3} from the bimetallic precursor contains the two metals in a better dispersion, resulting in a larger number of atomically dispersed surface Pt active sites. This catalyst gave more isomers (and methylcyclopentane) and fewer fragments and less benzene than the {open_quotes}traditional{close_quotes} sample. The {open_quotes}new{close_quotes} Pt-Sn/Al{sub 2}O{sub 3} sample possessed good long-term stability. The {open_quotes}traditional{close_quotes} sample lost some of its activity and its high hydrogenolysis selectivity during long use; i.e., it approached the catalytic properties of the {open_quotes}new{close_quotes} sample. Both samples are potential candidates as catalysts with high isomerizing and low aromatic selectivities (up to 75% isohexanes plus methylcyclopentane as opposed to a maximum of 20%, benzene). The results could be explained sufficiently with a geometric model, electronic interactions playing a less important role in the catalytic phenomena observed. 59 refs., 9 figs., 5 tabs.

OSTI ID:
539451
Journal Information:
Journal of Catalysis, Journal Name: Journal of Catalysis Journal Issue: 2 Vol. 168; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English

Similar Records

The effects of different preparation techniques on the characteristics of Pt-Sn/Al sub 2 O sub 3
Conference · Sat Aug 01 00:00:00 EDT 1987 · American Chemical Society, Division of Petroleum Chemistry, Preprints; (USA) · OSTI ID:5335954

Effects of the preparation techniques on the properties of Sn-Pt/Al sub 2 O sub 3 reforming catalysts
Conference · Sat Aug 01 00:00:00 EDT 1987 · American Chemical Society, Division of Petroleum Chemistry, Preprints; (USA) · OSTI ID:5426620

Conversion of n-hexane over Pt/Al sub 2 O sub 3 and Sn-Pt/Al sub 2 O sub 3 catalysts. A comprehensive reaction mechanism study
Conference · Sat Aug 01 00:00:00 EDT 1987 · American Chemical Society, Division of Petroleum Chemistry, Preprints; (USA) · OSTI ID:5335549