Methanol decomposition to synthesis gas over supported Pd catalysts prepared from synthetic anionic clays

Citation
R. Shiozaki et al., Methanol decomposition to synthesis gas over supported Pd catalysts prepared from synthetic anionic clays, CATAL LETT, 58(2-3), 1999, pp. 131-140
Citations number
26
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
CATALYSIS LETTERS
ISSN journal
1011372X → ACNP
Volume
58
Issue
2-3
Year of publication
1999
Pages
131 - 140
Database
ISI
SICI code
1011-372X(1999)58:2-3<131:MDTSGO>2.0.ZU;2-D
Abstract
Supported Pd or Rh catalysts were prepared by the solid-phase crystallizati on method starting from hydrotalcite anionic clay minerals based on [Mg6Al2 (OH)(16)CO32-]. 4H(2)O as the precursors. The precursors were prepared by a coprecipitation method from the raw materials containing Pd2+ and various trivalent metal ions which can replace each site of Mg2+ and Al3+ in the hy drotalcite. Rh3+ was also used for preparing the catalyst as comparison. Th e precursors were then thermally decomposed and reduced to form supported P d or Rh catalysts and used for the methanol decomposition to synthesis gas. Among the precursors tested, use of Mg-Cr hydrotalcite containing Pd2+ res ulted in the formation of efficient Pd supported catalysts for the producti on of synthesis gas by selective decomposition of methanol at low temperatu re. Although Pd2+ cannot well replace the Mg2+ site in the hydrotalcite, th e Pd supported catalyst (Pd/Mg-Cr) prepared by the solid-phase crystallizat ion method formed highly dispersed Pd metal particles and showed much highe r activity than that prepared by the conventional impregnation method. When the precursor was prepared under mild conditions, more fine particles of P d metal were formed over the catalyst, resulting in high activity. It is li kely that the high activity may be due to the highly dispersed and stable P d metal particles assisted by the role of Cr as the co-catalyst.