Distinguished Speaker Seminar - Department of Chemistry and Biochemistry
Friday, May 9, 2014
Rm. 0122, Chemistry Bldg. (Marker Seminar Room)
For More Information:
Department of Chemistry & Biochemistry
"Carbon Dioxide Capture and Hydrocarbon Separation in Metal-Organic Frameworks"
Professor Jeffrey R. Long
University of California, Berkeley
Senior Scientist, Materials Science Division
Lawrence Berkely National Laboratory
Owing to their high surface areas, tunable pore dimensions, and adjustable surface functionality, metal-organic frameworks (MOFs) can offer advantages for a variety of gas separation applications. In an effort to help curb emissions from power plants, we are developing new MOFs for use in post- and pre-combustion CO2 capture, and for the separation of O2 from air, as required for oxy-fuel combustion. In particular, MOFs with open metal cation sites or alkylamine-functionalized surfaces are demonstrated to provide high selectivities and working capacities for the adsorption of CO2 over N2 under dry flue gas conditions. Breakthrough measurements further show compounds of the latter type to be effective in the presence of water, while calorimetry data reveal a low regeneration energy compared to aqueous amine solutions. MOFs with open metal sites, such as Mg2(dobdc), are highly effective in the removal of CO2 under conditions relevant to H2 production, while redox-active Fe2+ sites in the isostructural compound Fe2(dobdc) allow the selective adsorption of O2 over N2. Fe2(dobdc) is further demonstrated to be effective for the fractionation of mixtures of C1 and C2 hydrocarbons, and for the separation of ethylene/ethane and propylene/propane mixtures. Finally, it will be shown that certain structural features possible within MOFs, but not in zeolites, can enable the fractionation of hexane isomers according to the degree of branching or octane number.