催化作用
吸附
活化能
降水
化学
氧化还原
动能
无机化学
物理化学
有机化学
物理
气象学
量子力学
作者
Hongling Guan,Jian Lin,Lin Li,Xiaodong Wang,Tao Zhang
标识
DOI:10.1016/j.apcatb.2015.11.040
摘要
Abstract A novel catalyst formulation of 3.1 wt.% Rh/Fe(OH) x was prepared via a co-precipitation method and investigated for CO preferential oxidation in H 2 -rich stream. This catalyst exhibited a wider temperature range of 20–70 °C for CO total removal and better resistance to CO 2 and H 2 O compared with the standard gold catalyst, standing out as the best Rh-based catalyst ever. The Rh species were highly dispersed in a subnano scale of ∼1 nm and improved the reducibility of Fe(OH) x support. The adsorption of O 2 was thus promoted over the reduced support, together with the weakened CO adsorption over the Rh clusters, permitting a non-competitive Langmuir–Hinshelwood mechanism through the elementary reaction of CO (ad) + O (ad) . The reaction rate equation of r = k [CO] 0.73 [O 2 ] 0.64 and small apparent activation energy of 24 kJ mol −1 were then derived from the kinetic studies.
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