As a single phase, doped BaCeO3 exhibits one of the highest proton stability and conductivity up to 600-700 °C, although it is chemically instable due to carbonation formation by exposure to moist reducing atmospheres. [1] Contrarily, some ion conducting doped CeO2 has demonstrated to be stable in CO2, SO2, H2O containing atmospheres at high temperature. [2, 3] Several authors have shown the chemical compatibility and stability in fuel cell operation and syngas conditions of systems based on doped BaCe1-xMxO3-δ and Ce1-xMxO2-δ containing similar dopants in both phases. [4-6]
The present work shows the evaluation of stability of composite membranes made of nominal BaCe0.8M0.2O3-δ (BCMO, M= Y, Eu, Sm, Tb, Gd, Nd ) and Ce0.8X0.2O2-δ (CXO, X= Y, Eu, Sm, Tb, Gd, Nd) in operating gases for WGSR. The two crystalline phases were synthesized separately via the conventional solid-state route at 1400 °C and combined in a cer-cer composite with 50:50 volume ratio. Dense pellets were prepared by calcining uniaxially pressed pellets at 1600 °C. Although both perovskite and fluorite phases are well distinguished, Rietveld refinement on XRD patterns in addition to SEM-EDS analysis of fresh-reference pellets revealed the migration of the M to the ceria phase, in disagreement with previously cited literature. However, the electrochemical properties of these composites measured by AC-conductivity still show a substantial improvement regarding the pristine single phase materials.
The highest conductivity among the tested composites was found for BaCe0.8Eu0.2O3-δ (BCEO):Ce0.8Y0.2O2-δ (CYO). Thus, a more comprehensive study was made. DC conductivity was measured in dry and wet H2, and D2 atmospheres (where H2 and D2 were 5% in He, and pH2O and pD2O correspond to 0.025 atm). Results suggested that electrons and/or oxygen ions are the predominant charge carriers in the studied temperature range. Hydrogen permeation higher than 0.6 ml·cm-2·min-1 was achieved at 700 °C, when 50% H2 in He was used as feed gas and humidified Ar for sweeping (pH2O=0.042 atm). This value approaches the target of 1 ml·cm-2·min-1 for proton conducting ceramics. By adding 15 vol% CO2 in the feeding stream, chemical stability was demonstrated at 700 °C.
The stability tests have been performed at 600-900 °C in syngas (WGSR feed) that contained 15% H2, 34% CO and 51% H2O (volume %); and in retentate simulating conditions that contained 0.1% H2, 90% CO2 and 9.9% H2O. XRD and SEM analysis after the exposure shows the decomposition of the BCLnO phase at low temperatures and the formation of carbonates. However, the carbonate peaks disappear at 900 °C and 800 °C for some of the compounds. As evidenced in former studies [4] materials with this dual phase sustain their microstructures and phase characteristics under selected conditions (15 vol% CO2 at 700 °C). This entails these materials as suitable for other catalytic membrane reaction applications.
References
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[2] M. Balaguer, C. Solís, J.M. Serra, Structural–Transport Properties Relationships on Ce1–xLnxO2−δ System (Ln = Gd, La, Tb, Pr, Eu, Er, Yb, Nd) and Effect of Cobalt Addition, The Journal of Physical Chemistry C, 116 (2012) 7975-7982.
[3] M. Balaguer, J. García-Fayos, C. Solís, J.M. Serra, Fast Oxygen Separation Through SO2- and CO2-Stable Dual-Phase Membrane Based on NiFe2O4–Ce0.8Tb0.2O2-δ, Chemistry of Materials, 25 (2013) 4986-4993.
[4] S. Elangovan, B.G. Nair, T.A. Small, Ceramic mixed protonic/electronic conducting membranes for hydrogen separation, in, Google Patents, 2007.
[5] S. Ricote, A. Manerbino, N.P. Sullivan, W.G. Coors, Preparation of dense mixed electron- and proton-conducting ceramic composite materials using solid-state reactive sintering: BaCe0.8Y0.1M0.1O3−δ–Ce0.8Y0.1M0.1O2−δ (M=Y, Yb, Er, Eu), J Mater Sci, 49 (2014) 4332-4340.
[6] D. Medvedev, E. Pikalova, A. Demin, A. Podias, I. Korzun, B. Antonov, P. Tsiakaras, Structural, thermomechanical and electrical properties of new (1 − x)Ce0.8Nd0.2O2−δ–xBaCe0.8Nd0.2O3−δ composites, Journal of Power Sources, 267 (2014) 269-279.