(619d) Sintering of Copper-Based Catalysts for Methanol Synthesis From Carbon Dioxide | AIChE

(619d) Sintering of Copper-Based Catalysts for Methanol Synthesis From Carbon Dioxide


Abdelsayed, V., National Energy Technology Laboratory
Ohodnicki, P. R. Jr., National Energy Technology Laboratory
Howard, B. H., National Energy Technology Laboratory
Lekse, J., US DOE, National Energy Technology Laboratory
Deng, X., Lawrence Berkeley National Laboratories
Matranga, C., National Energy Technology Laboratory

Hydrogenation of carbon dioxide to methanol over Cu-based catalysts has been considered a viable pathway to reduction of greenhouse gas emissions.  Under typical reaction conditions, catalyst deactivation is primarily attributed to loss of active surface area and is accelerated by water vapor byproduct.  Therefore, Cu sintering remains one of the most significant technical barriers to the effective use of these catalytic systems.

Our approach for enhancing sintering resistance is to add promoters that can help suppress the crystallization of active catalytic phases during thermal treatment.  We have examined the sintering of Cu-based catalysts designed specifically for methanol synthesis from CO2 using various techniques including N2O decomposition, X-ray diffraction (XRD), and transmission electron microscopy (TEM).  The incorporation of gallium and yttrium oxides into our catalyst formulations is effective in maintaining high Cu dispersion, therefore leading to significant improvement in the overall performance.  Interestingly, ZnO remains well-dispersed or XRD-amorphous in best-performing catalysts.  We have also attempted to fit sintering data to a model that can predict a limiting Cu dispersion at infinite time.  Kinetic parameters such as rate constant and deactivation order obtained from curve fitting provide new insight into possible sintering mechanisms.  These findings have important implications for the rational design of robust catalytic systems for CO2 conversion to fuels and chemicals.

See more of this Session: Catalyst Deactivation II

See more of this Group/Topical: Catalysis and Reaction Engineering Division