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   <subfield code="a">Cobalt Ferrite in YSZ for Use as Reactive Material in Solar Thermochemical Water and Carbon Dioxide Splitting, Part II: Kinetic Modeling</subfield>
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   <subfield code="c">[Kyle Allen, Nick Auyeung, Nima Rahmatian, James Klausner, Eric Coker]</subfield>
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   <subfield code="a">The kinetics of 10wt.% cobalt ferrite (CoFe2O4) in 8mol.% yttria-stabilized zirconia, synthesized via the co-precipitation method and formed into a porous structure, are investigated in support of simulating the performance of a solar thermochemical reactor. Kinetic parameters for the thermal reduction (T-R) of CoFe2O4 at temperatures of 1325-1500°C were investigated by thermogravimetry. A nonlinear best fit of a uniform conversion model was used to determine kinetic parameters from experimental data. In the temperature range of 1375-1450°C, the activation energy and preexponential term were found to be 386±13kJmol−1 and 8.8×109±2.0×108min−1, respectively, while increasing at higher temperatures. Simultaneous thermogravimetric analysis and differential scanning calorimetry studies showed an increase in the reaction rate of T-R upon the onset of melting (1440°C). Oxidation studies of the material using CO2 yield an activation energy and preexponential term of 52.1±6.8kJmol−1 and 2.86±0.2min−1, respectively, which is in good agreement with past work. The reaction order for CO2 was determined to be 0.750±0.08. The reaction kinetics for oxidation using CO2 were best described by a 3-D diffusion Jander model.</subfield>
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