Examination of Perovskite Structure CaMnO 3-δ with MgO Addition as Oxygen Carrier for Chemical Looping with Oxygen Uncoupling Using Methane and Syngas
Artikel i vetenskaplig tidskrift, 2013

Perovskite structure oxygen carriers with the general formula CaMn x Mg 1-x O 3-δ were spray-dried and examined in a batch fluidized bed reactor. The CLOU behavior, reactivity towards methane, and syngas were investigated at temperature 900°C to 1050°C. All particles showed CLOU behavior at these temperatures. For experiments with methane, a bed mass corresponding to 57 kg/MW was used in the reactor, and the average CH 4 to CO 2 conversion was above 97% for most materials. Full syngas conversion was achieved for all materials utilizing a bed mass corresponding to 178 kg/MW. SEM/EDX and XRD confirmed the presence of MgO in the fresh and used samples, indicating that the Mg cation is not incorporated into the perovskite structure and the active compound is likely pure CaMnO 3-δ . The very high reactivity with fuel gases, comparable to that of baseline oxygen carriers of NiO, makes these perovskite particles highly interesting for commercial CLC application. Contrary to NiO, oxygen carriers based on CaMnO 3-δ have no thermodynamic limitations for methane oxidation to CO 2 and H 2 O, not to mention that the materials are environmentally friendly and can utilize much cheaper raw materials for production. The physical properties, crystalline phases, and morphology information were also determined in this work. © 2013 Dazheng Jing et al.

Författare

Dazheng Jing

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Tobias Mattisson

Chalmers, Energi och miljö, Energiteknik

Henrik Leion

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Magnus Rydén

Chalmers, Energi och miljö, Energiteknik

Anders Lyngfelt

Chalmers, Energi och miljö, Energiteknik

International Journal of Chemical Engineering

1687-806X (ISSN) 1687-8078 (eISSN)

Vol. 2013 679560

Ämneskategorier

Materialteknik

Kemiteknik

Styrkeområden

Energi

Materialvetenskap

DOI

10.1155/2013/679560