Session Information
14th Annual Green Chemistry and Engineering Conference
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Carbon capture and utilization through chemical looping dry reforming
Track : June 22, 2010
Program Code: 183
Date: Tuesday, June 22, 2010
Time: 2:40 PM to 3:00 PM  EST
Location: Capital Hilton - Federal B
CONTRIBUTOR (S):
Rahul Solunke, Department of Chemical Engineering, University of Pittsburgh, Pittsburgh, PA, United States
Goetz Veser, Mascaro Center for Sustainable Innovation, University of Pittsburgh, Pittsburgh, PA, United States
Todd Gardner, National Energy Technology Laboratory, U.S. Department of Energy, Pittsburgh, PA, United States
SPEAKER :
Michelle Najera, Department of Chemical Engineering / Mascaro Center for Sustainable Innovation, University of Pittsburgh, Pittsburgh, PA, United States
Description
Chemical looping combustion (CLC) has been demonstrated as a clean combustion technology, which produces high purity, high-pressure, sequestration-ready CO2 streams from both fossil and renewable fuels. CLC is based on a two reactor concept in which flameless, NOx-free combustion is achieved by contacting a fuel with a solid oxygen carrier material in the first reactor, followed by the re-oxidation of the carrier with air in the second reactor. However, while CLC is a highly efficient technology for CO2 capture, it does not present a solution to CO2 sequestration.

Here, an alternate chemical looping concept, Chemical Looping Dry Reforming (CLDR), is proposed. In CLDR, air is replaced by CO2 as the oxidizing gas. This process thus results in the catalytic activation of CO2 via reduction to CO and thus potentially opens a novel pathway towards CO2 utilization.

We will present results from a feasibility study, which includes thermodynamic screening for potential oxygen carriers, synthesis and characterization of promising nanostructured carriers, and kinetic testing of select carrier materials in cyclic thermal gravimetric analysis (TGA) and fixed-bed reactor studies. Our results indicate that it is indeed possible to reduce CO2 to CO with high reaction rates even at very mild temperatures (as low as 200oC) via use of appropriately designed nanostructured carriers, and to integrate this step into a cyclic redox (“looping”) process as described above.


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