Journal
APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 269, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.apcatb.2020.118758
Keywords
Chemical looping; Lattice oxygen; Hydrogen generation; Methanol reforming; Catalytic oxygen carrier
Funding
- National Natural Science Foundation of China [21525626, 51761145012, U1663224]
- Program of Introducing Talents of Discipline to Universities [B06006]
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Auto-thermal reforming of methanol is an attractive route for low-temperature methanol conversion for hydrogen production. This paper describes utilization the lattice oxygen of Cu2O/Ca2Fe2O5 participates the partial oxidation of methanol to achieve the efficient auto-thermal reforming of methanol. ASPEN Plus software was adopted to verify the feasibility of auto-thermal conversion of methanol via Cu <-> Cu2O looping and provided a comprehensive understanding of the associated process via operating parameter optimization. A series of CuO/Ca2Fe2O5 with different contents of copper were prepared as the catalytic oxygen carrier (COC) which goes through the reduction -> catalytic methanol conversion -> re-oxidation. The surface and bulk properties of COCs were characterized by XRD, XPS, TEM-EDS mapping, Raman, and H-2-TPR; the reaction pathways were investigated using CH3OH-pulse and in situ DRIFTS. Results indicate that 40 % Cu-loaded Cu2O-Ca2Fe2O5 shows the highest catalytic activity of the synthesized COCs, and the presence of Ca2Fe2O5 tunes the redox activity and mobility of the lattice oxygen, obtaining a H-2 production rate of 37.6 mu mol.H-2.g(-1).COG.s(-1) at 240 degrees C. The reaction pathways of chemical looping methanol conversion follow the sequence: CH3OH full oxidation -> formaldehyde intermediate -> methyl-formate intermediate as the amount of lattice oxygen decreases gradually.
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