Support conductive metal oxide

Wang et al. proposed some strategies to develop durable catalyst supports, using graphitized carbons as scaffolds and protecting die carbon surface with tungsten carbide, oxycarbides, or conductive metal oxides [69]. Unfortunately, no durability results were reported. 

Although catalytic wet oxidation of acetic acid, phenol, and p-coumaric acid has been reported for Co-Bi composites and CoOx-based mixed metal oxides [3-5], we could find no studies of the wet oxidation of CHCs over supported CoO catalysts. Therefore, this study was conducted to see if such catalysts are available for wet oxidation of trichloroethylene (TCE) as a model CHC in a continuous flow fixal-bed reactor that requires no subsequent separation process. The supported CoOx catalysts were characterized to explain unsteady-state behavior in activity for a certain hour on stream. 

The oxides of Si, Al, Ti, Zr, Ca, Mg, and Zn have often served as convenient supports for metal nanoclusters [358-362]. Conductive glassy carbon or graphite materials have proved to be suitable carriers for electrocatalytic applications [363,364]. 

Platinum and Palladium Based Catalysts. Researchers at ANL have also developed an ATR catalyst formulation comprised of a transition metal element supported on an oxide ion-conducting substrate, such as ceria. 

Initially tests were conducted in glass equipment at atmospheric pressure. It was discovered that a more durable catalyst could be made if the Group VI metal oxide were deposited on an alumina support. The best support found for this reaction was alumina, and the first commercial catalyst was made by impregnating a material very similar to activated alumina 1 with a molybdenum salt solution, followed by drying and calcining at a temperature above 1000° F. Interestingly enough, the supported chromia catalyst which showed a marked superiority over the supported molybdena catalyst at atmospheric... 

---