TY - JOUR
T1 - Ruthenium substituted pyrochlore metal oxide catalysts Y2Ce2-xRuxO7-δ (x = 0–0.4) for oxidative steam reforming of ethanol
AU - Hsieh, Ho Chen
AU - Chen, Yun Sheng
AU - Weng, Sheng Feng
AU - Hsieh, Yu Ping
AU - Lee, Chi-Shen
PY - 2020/7/31
Y1 - 2020/7/31
N2 - Metal oxides Y2Ce2-xRuxO7-δ (x = 0–0.4) with partial substitution of Run+ cations in the host structure were synthesized to study their catalytic activity on oxidative steam reforming of ethanol (OSRE). The samples were characterized using X-ray diffraction (XRD), X-ray photoelectron spectra (XPS) and temperature-programmed reduction (TPR). The performances investigated by varied temperatures, Ru ion content, carbon-to-oxygen ratios and long-term stability. The lowest activation temperature on OSRE is 300 °C, which is significantly lower than that of La2Ce2-xRuxO7-δ (400 °C). The cell dimension of Y2Ce2-xRuxO7-δ was reduced compare to La2Ce2-xRuxO7-δ for the replacement of the Y3+ ion with La3+ ion. The reduced unit cell in the host structure not only increase the surface composition of the Ce4+ ions, but also induce the synergetic effect of Run+/Ru4+ (n > 4) and Ce4+/Ce3+, which lead to the enhanced OSRE activity. The optimized catalyst Y2Ce1.6Ru0.4O7-δ showed selectivity of hydrogen SH2 = 84(4)% (YH2 = 2.5(1) mol/mol EtOH) and carbon monoxide SCO = 48(1)% for long-term stability test at T = 300 °C, C/O = 0.5, and O2/C2H5OH = 1.5.
AB - Metal oxides Y2Ce2-xRuxO7-δ (x = 0–0.4) with partial substitution of Run+ cations in the host structure were synthesized to study their catalytic activity on oxidative steam reforming of ethanol (OSRE). The samples were characterized using X-ray diffraction (XRD), X-ray photoelectron spectra (XPS) and temperature-programmed reduction (TPR). The performances investigated by varied temperatures, Ru ion content, carbon-to-oxygen ratios and long-term stability. The lowest activation temperature on OSRE is 300 °C, which is significantly lower than that of La2Ce2-xRuxO7-δ (400 °C). The cell dimension of Y2Ce2-xRuxO7-δ was reduced compare to La2Ce2-xRuxO7-δ for the replacement of the Y3+ ion with La3+ ion. The reduced unit cell in the host structure not only increase the surface composition of the Ce4+ ions, but also induce the synergetic effect of Run+/Ru4+ (n > 4) and Ce4+/Ce3+, which lead to the enhanced OSRE activity. The optimized catalyst Y2Ce1.6Ru0.4O7-δ showed selectivity of hydrogen SH2 = 84(4)% (YH2 = 2.5(1) mol/mol EtOH) and carbon monoxide SCO = 48(1)% for long-term stability test at T = 300 °C, C/O = 0.5, and O2/C2H5OH = 1.5.
KW - Oxidative ethanol steam reforming
KW - Pyrochlore structure
KW - Solid oxide catalyst
KW - Solid solution structure
UR - http://www.scopus.com/inward/record.url?scp=85086031115&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2020.05.080
DO - 10.1016/j.ijhydene.2020.05.080
M3 - Article
AN - SCOPUS:85086031115
SN - 0360-3199
VL - 45
SP - 19291
EP - 19303
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 38
ER -