共 21 条
Highly Active Cobalt Oxide Catalysts Prepared by SACOP for the Preferential Oxidation of CO in Excess Hydrogen
被引:12
作者:
Lopez, Irene
[1
]
Valdes-Solis, Teresa
[1
]
Marban, Gregorio
[1
]
机构:
[1] Inst Nacl Carban INCAR CSIC, Dept Chem Mat, Funct Porous Mat Grp, Oviedo 33011, Spain
来源:
关键词:
carbon dioxide;
cobalt;
heterogeneous catalysis;
hydrogen;
SELECTIVE OXIDATION;
CARBON-MONOXIDE;
KINETICS;
PROX;
H-2;
D O I:
10.1002/cctc.201000351
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Cobalt based catalysts synthesized by the silica aquagel confined co-precipitation (SACOP) method and analyzed at high spatial velocities (approximate to 39000 h(-1)) for the preferential oxidation (PROX) of CO in the presence of hydrogen showed the highest values of catalytic activity of all the cobalt-based catalysts described in the literature, together with good values of selectivity and stability. The Co(3)O(4)/CoOOH nanocatalysts had specific surface areas of up to 120 m(2)g(-1) depending on the type of precipitation used. The SACOP samples precipitated by pouring aquagel into the NaOH solution (method A) gave rise to samples with less CoOOH than if the NaOH solution was poured over the aquagel (method B). This difference is ascribed to the migration of cobalt out of the aquagel microstructure during precipitation by method A. Precipitation by means of method B produced the most active catalyst, owing to the larger amount of amorphous CoOOH in the fresh sample, which was formed by the removal of silica from the cobalt silicate hydroxide. The CoOOH is gradually reduced to high surface area Co(3)O(4) in the presence of H(2) during the PROX reaction. The mechanisms of formation of CoOOH and Co(3)O(4) by using SACOP are also discussed.
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页码:734 / 740
页数:7
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