Investigation of Pt/γ-Al2O3 catalysts with locally high Pt concentrations for oxidation of CO at low temperatures
Journal article, 2004

A new method for preparing supported catalysts, in which Pt was distributed in locally high concentrations on the γ-Al2O3 support, was studied. These catalysts were compared with a conventionally prepared Pt/γ-Al2O3 catalyst in which Pt was deposited evenly on the support. The object was to ascertain whether it is possible to prepare catalysts that retain heat released from exothermic reactions to a higher extent and thereby become more low-temperature active than a conventionally prepared catalyst. A significant improvement of the activity was observed for the catalysts prepared with locally high Pt concentrations when CO (1%, 1000 and 100 ppm) was oxidized at a constant O2 concentration (10%). The improved activity is discussed in terms of heat transfer, mass transfer, and structure sensitivity. Differences in heat transfer appear to be the least probable reason for the enhanced activity for the catalysts with locally higher Pt concentrations, whereas structural effects also seem to be an unlikely explanation. Differences in mass transfer seem, however, to be a more likely reason for the improved activity.

Alumina

Platinum

CO oxidation

Low temperature

Structure sensitivity

Mass transport

Catalytic activity

Heat transport

Author

Karl Arnby

Competence Centre for Catalysis (KCK)

Chalmers, Chemical and Biological Engineering, Applied Surface Chemistry

A. Torncrona

Eka Chemicals AB

Perstorp Formox

Bengt Andersson

Chalmers, Chemical and Biological Engineering, Chemical Reaction Engineering

Competence Centre for Catalysis (KCK)

Magnus Skoglundh

Competence Centre for Catalysis (KCK)

Chalmers, Chemical and Biological Engineering, Applied Surface Chemistry

Journal of Catalysis

0021-9517 (ISSN) 1090-2694 (eISSN)

Vol. 221 1 252-261

Driving Forces

Sustainable development

Areas of Advance

Nanoscience and Nanotechnology (2010-2017)

Transport

Energy

Materials Science

Subject Categories

Chemical Engineering

Environmental Sciences

DOI

10.1016/j.jcat.2003.08.017

More information

Created

10/7/2017