Solar Thermal H2O Splitting Via Cobalt Ferrite Based Thermochemical Cycles

  • Type:
    Conference Presentation
  • Conference Type:
    AIChE Annual Meeting
  • Presentation Date:
    November 11, 2009
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Spinel ferrites of the form MxFe3-xO4, where M generally represents Ni, Zn, Co, Mn, Fe or other transition metals, have been shown to be capable of splitting water to produce H2 using solar energy according to the two step cycle shown below: MxFe3-xO4 xMO + (3-x)FeO + 0.5 O2 (1) xMO + (3-x)FeO + H2O MxFe3-xO4 + H2 (2) The first, high temperature reduction step occurs at temperatures ranging between 1400 oC to 1500 oC. In the second lower temperature step (~1000 oC), the reduced sample is reacted with steam to regenerate the ferrite and produce H2. Currently, little is understood about the kinetics and mechanisms of these reactions. We are reporting the results of a kinetic study of the water oxidation (WO) reaction of cobalt ferrites (CoxFe3-xO4), in which the effect of temperature, water concentration, mass loadings and Co/Fe ratio was studied. Ferrites were synthesized via atomic layer deposition (ALD) on high surface area (50 m2/g and 90 m2/g) ZrO2 monoliths of various surface areas. This technique has the advantage of being able to precisely control the thickness and Co/Fe ratio on the atomic level, resulting in well defined, homogenous samples. A high temperature stagnation flow reactor was used to carry out both the high temperature reduction step, and the lower temperature water splitting step. Preliminary results indicate that both water concentration, as seen in figure 1, and temperature have a significant impact upon the H2 reaction rate. Even though water flowrate is 100 times higher than the H2 reaction rate when flowing only 1% H20, the water concentration was rate limiting up to concentrations of 15%. Additionally, the Co/Fe ratio had an effect on the H2 reaction rate. Fe3O4 was characterized by a rapid H2 increase followed by a rapid decrease. However, CoFe2O4 was characterized by a rapid H2 increase followed by a slow decrease in H2 over time. A shrinking core model, coupled with O2 diffusion coefficients in Fe3O4 found in the literature, has been fit to experimental data, as shown in figure 2. Hydrogen evolution was measured in situ using a mass spectrometer, and oxidation state changes were observed in situ via Raman spectroscopy. Surface area was measured via BET analysis, and film composition was determined by ICP-AES and XRD analysis. Figure 1. H2 reaction rate as function of time for water concentrations ranging from 3.65 to 29.42% Figure 2. Shrinking core model coupled with O2 diffusion characterizes experimental data well&'



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