TY - JOUR
T1 - Pt-Ce0.9Cu0.1O2/activated carbon as highly active and stable HI decomposition catalyst
AU - Punkrawee, Wachirapun
AU - Yamanaka, Azusa
AU - Matsuda, Junko
AU - Mitoma, Yukiko
AU - Nishiyama, Noriko
AU - Ishihara, Tatsumi
N1 - Funding Information:
This work was supported by the Council for Science, Technology, and Innovation (CSTI), Cross‐ministerial Strategic Innovation Promotion Program (SIP), and “Energy Carriers” (Funding agency JST).
Publisher Copyright:
Copyright © 2017 John Wiley & Sons, Ltd.
PY - 2018/3/10
Y1 - 2018/3/10
N2 - Effects of additives to Pt-CeO2/activated carbon (M563) catalysts on HI decomposition were studied. Among the additives studied, it was found that the addition of Cu to Pt-CeO2 is the most effective for increasing the catalytic activity to HI decomposition. On this catalyst, almost the equilibrium hydrogen iodide (HI) conversion was achieved at temperature higher than 573 K. Cu addition increased Pt dispersion by anchoring effects. Therefore, in spite of decreased Brunauer-Emmett-Teller surface area of the catalyst, dispersion of Pt was much increased by addition of Cu resulting in the increased HI decomposition activity and stability. Because formed I2 adsorbed on the catalyst at initial ca 20 hours, HI conversion was higher than that of the equilibrium one; however, after 20 hours, stable HI decomposition conversion that was almost the same with equilibrium conversion was achieved in the examined temperature range.
AB - Effects of additives to Pt-CeO2/activated carbon (M563) catalysts on HI decomposition were studied. Among the additives studied, it was found that the addition of Cu to Pt-CeO2 is the most effective for increasing the catalytic activity to HI decomposition. On this catalyst, almost the equilibrium hydrogen iodide (HI) conversion was achieved at temperature higher than 573 K. Cu addition increased Pt dispersion by anchoring effects. Therefore, in spite of decreased Brunauer-Emmett-Teller surface area of the catalyst, dispersion of Pt was much increased by addition of Cu resulting in the increased HI decomposition activity and stability. Because formed I2 adsorbed on the catalyst at initial ca 20 hours, HI conversion was higher than that of the equilibrium one; however, after 20 hours, stable HI decomposition conversion that was almost the same with equilibrium conversion was achieved in the examined temperature range.
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U2 - 10.1002/er.3903
DO - 10.1002/er.3903
M3 - Article
AN - SCOPUS:85042111303
SN - 0363-907X
VL - 42
SP - 1088
EP - 1097
JO - International Journal of Energy Research
JF - International Journal of Energy Research
IS - 3
ER -