Chemical looping combustion (CLC) processes have been shown to be promising and effective in reducing CO2 production from the combustion of various fuels associated with the growing global demand for energy, as it promotes indirect fuel combustion through solid oxygen carriers (SOC). Thus, this study aims to synthesize, characterize and evaluate mixed copper and titanium oxide as a solid oxygen carrier for use in combustion processes with chemical looping. The SOC was synthesized based on stoichiometric calculations by the polymeric precursor method and characterized by: X-ray fluorescence (XRF), X-ray diffraction (XRD), Scanning Electron Microscopy (SEM-FEG) with EDS, and Programmed Temperature Reduction (PTR). The oxygen carrying capacity (ROC) and the speed index of the reduction and oxidation cycles were evaluated by Thermogravimetric Reactivity (TGA). The main reactive phase identified was: The CuO phase for the mixed copper and titanium oxide were identified and confirmed by X-ray diffraction using the Rietveld refinement method. The reactivity of the CuO-TiO2 system was high, obtaining a CH4 conversion rate above 90% and a speed index of 40%/min. Due to the structural characteristics and the reactivity tests of this material, it is concluded that mixed copper and titanium oxide have the necessary requirements to be used in chemical looping combustion (CLC) processes.
Chemical Looping Combustion (CLC) technology has emerged as a promising alternative capable of restricting the effects of global warming due to anthropogenic gas emissions, especially CO2, through its inherent capture. This study aims to synthesize and evaluate Cu-based oxygen carriers supported on natural materials such as diatomite and kaolin, through the incipient wet impregnation method for CLC process applications. Oxygen carriers were characterized by X-ray diffraction (XRD), temperature-programmed reduction (TPR), and scanning electron microscopy with surface energy dispersive x-ray spectroscopy (SEM-EDS). The mechanical strength of the two oxygen carrier particles was determined after the sintering procedure resulting in high crushing force. Reactivity of oxygen carriers was evaluated in a thermobalance with CH4 and H2 gases. Different reaction pathways were attempted when undergoing the redox cycles: total direct reduction of CuO to Cu0 for Cu-K and partial reduction of CuO to Cu2O and CuO to Cu-D. However, the highest reactivity and reaction rate was achieved in Cu-D due to the pore structure of diatomite, the chemical composition and the resulting interaction between CuO and the support. H2 gas reactivity tests showed a higher conversion rate and greater stability between cycles for both oxygen carriers. Thus, the reducible CuO content present in Cu-Diatomite during the reactivity test with H2 as the fuel gas was ideal for achieving high solids conversion, tendency for greater stability and a higher reaction rate.
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