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Microwave Synthesis of Metallic Nanoparticles Supported on Porous Coordination Polymers: A Bi-functional Catalyst Design for CO2 Activation and Conversion

Published online by Cambridge University Press:  01 March 2011

Victor Abdelsayed
Affiliation:
National Energy Technology Laboratory, 3610 Collins Ferry Rd., Morgantown, WV 26507, USA URS Corporation, 3610 Collins Ferry Rd., Morgantown, WV 26507, USA
Yueying Fan
Affiliation:
National Energy Technology Laboratory, 3610 Collins Ferry Rd., Morgantown, WV 26507, USA URS Corporation, 3610 Collins Ferry Rd., Morgantown, WV 26507, USA
Todd Gardner*
Affiliation:
National Energy Technology Laboratory, 3610 Collins Ferry Rd., Morgantown, WV 26507, USA
*
*Corresponding author.
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Abstract

The efficient separation and conversion of CO2 from power plant flue gases remains a significant and far reaching global goal. Partially, because of the high energy cost associated with CO2 separation which makes technologies, such as amine scrubbing and conventional sorbent materials, less attractive. In this work we have used a microwave-assisted method to prepare Mg-based porous coordination polymers (MOF-74) with open metal sites. The material shows a high CO2 uptake at room temperature mainly due to the high binding energy between the open Mg site (in the coordination polymer) and the oxygen atom of the adsorbed CO2 molecule. Our results show that the microwave-based Mg-MOF-74 shows superior properties compared to thermally prepared samples such as higher surface area, crystallinity and CO2 uptake. Pt nanoparticles (<5-10 nm) were deposited on the Mg-MOF-74 as manifested from the TEM results. The Pt nanoparticles were uniformly dispersed across the sample with more aggregations at higher Pt loadings. Different techniques were used to characterize the materials such as (BET surface area, XRD, SEM, EDS, TEM and TGA). These materials function as a bi-functional catalyst and sorbent material with the Mg-MOF-74 material responsible for CO2 capture and supported Pt nanoparticles responsible for its catalytic activity.

Type
Research Article
Copyright
Copyright © Materials Research Society 2011

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References

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