Abstract
Monometallic palladium catalysts were synthesized using different titanium supports and tested for the reduction of nitrates from aqueous solutions using hydrogen as a reductant. The Pd/TiO2 catalysts were characterized by electron paramagnetic resonance (EPR), low-temperature Fourier transform infrared (FTIR) spectroscopy of adsorbed CO, and X-ray diffraction (XRD). The catalysts studied exhibited a high activity for nitrate removal with a lower tendency for nitrite formation than the conventional bimetallic Pd catalysts. Although ammonium formation was greater than desired, the use of a monometallic catalyst for this two-step reduction process is significant and suggests that a single site may be responsible for both reduction stages. The titanium support (particularly the Ti3+ centers generated during prereduction in the presence of Pd) appear to play an important role in the nitrate degradation process. The potential role of Pd beta-hydride in generating these Ti3+ centers is discussed. (c) 2005 Elsevier Inc. All rights reserved.
Original language | English |
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Pages (from-to) | 282-291 |
Number of pages | 9 |
Journal | Journal of Catalysis |
Volume | 234 |
DOIs | |
Publication status | Published - Jun 2005 |
Keywords
- Pd/TiO2
- low-temperature Fourier transform infrared spectroscopy
- nitrate reduction
- aqueous solutions
- METAL-SUPPORT INTERACTION
- ELECTRON-PARAMAGNETIC-RES
- PD-CU CATALYSTS
- DRINKING-WATER
- SELECTIVE HYDROGENATION
- PD/TIO2 CATALYSTS
- CARBON-MONOXIDE
- CO ADSORPTION
- PALLADIUM
- TITANIUM