Catalysts for the Selective Oxidation of Methanol
AbstractIn industry, one of the main catalysts typically employed for the selective oxidation of methanol to formaldehyde is a multi-component oxide containing both bulk Fe2(MoO4)3 and excess MoO3. It is thought that the excess MoO3 primarily acts to replace any molybdenum lost through sublimation at elevated temperatures, therefore preventing the formation of an unselective Fe2O3 phase. With both oxide phases present however, debate has arisen regarding the active component of the catalyst. Work here highlights how catalyst surfaces are significantly different from bulk structures, a difference crucial for catalyst performance. Specifically, Mo has been isolated at the surface as the active surface species. This leaves the role of the Fe in the catalyst enigmatic, with many theories postulated for its requirement. It has been suggested that the supporting Fe molybdate phase enables lattice oxygen transfer to the surface, to help prevent the selectivity loss which would occur in the resulting oxygen deficit environment. To assess this phenomenon in further detail, anaerobic reaction with methanol has been adopted to evaluate the performance of the catalyst under reducing conditions. View Full-Text
Scifeed alert for new publicationsNever miss any articles matching your research from any publisher
- Get alerts for new papers matching your research
- Find out the new papers from selected authors
- Updated daily for 49'000+ journals and 6000+ publishers
- Define your Scifeed now
Brookes, C.; Bowker, M.; Wells, P.P. Catalysts for the Selective Oxidation of Methanol. Catalysts 2016, 6, 92.
Brookes C, Bowker M, Wells PP. Catalysts for the Selective Oxidation of Methanol. Catalysts. 2016; 6(7):92.Chicago/Turabian Style
Brookes, Catherine; Bowker, Michael; Wells, Peter P. 2016. "Catalysts for the Selective Oxidation of Methanol." Catalysts 6, no. 7: 92.
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.