Abstract
Many gold catalysts have been actively surveyed, but Au/SiO2 catalysts that are highly active for CO oxidation still remain evasive. In this work, gold nanoparticles well dispersed on Cab-O-Sil fumed SiO2 were prepared using Au(en)2Cl3 (en = ethylenediamine) as the precursor, and found to be very active for CO oxidation below 0 °C. The catalyst pretreatment via reduction and calcination, effect of gold loading, post-treatment in acidic and basic media, catalyst deactivation, storage, regeneration, and effect of surface modification by other metal oxides were explored. The results provide new perspective on the activation and promotion of active Au/SiO2-based catalysts.
Original language | English |
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Pages (from-to) | 89-99 |
Number of pages | 11 |
Journal | Applied Catalysis A: General |
Volume | 326 |
Issue number | 1 |
DOIs | |
State | Published - Jun 30 2007 |
Funding
This work was supported by the Office of Basic Energy Sciences, U.S. Department of Energy. The Oak Ridge National Laboratory is managed by UT-Battelle, LLC for the U.S. DOE under Contract DE-AC05-00OR22725. This research was supported in part by the appointment for H.G. Zhu, Z. Ma, and J.C. Clark to the ORNL Research Associates Program, administered jointly by ORNL and the Oak Ridge Associated Universities.
Keywords
- Au(en)Cl
- CO oxidation
- Gold catalysis
- Nanoparticles
- Silica