Steam Reforming of Bio-Ethanol to Produce Hydrogen over Co/CeO2 Catalysts Derived from Ce1-xCoxO2-y Precursors

被引:18
作者
Liu, Yanyong [1 ]
Murata, Kazuhisa [1 ]
Inaba, Megumu [1 ]
机构
[1] AIST, Natl Inst Adv Ind Sci & Technol, Res Inst Energy Frontier, Onogawa 16-1, Tsukuba, Ibaraki 3058569, Japan
关键词
bio-ethanol; steam reforming; hydrogen; urea hydrolysis; homogeneous precipitation; Co; CeO2; catalyst; Ce1-xCoxO2-y mixed oxide; solid-phase crystallization; SUPPORTED COBALT CATALYSTS; LOW-TEMPERATURE; METHANOL DECOMPOSITION; REACTION-MECHANISM; MIXED ALCOHOLS; IN-SITU; CU/ZNO; SYNGAS; CO; OXIDE;
D O I
10.3390/catal6020026
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
A series of Ce1-xCoxO2-y precursors were prepared by homogeneous precipitation using urea as a precipitant. The Co/CeO2 catalysts obtained from the Ce1-xCoxO2-y precursors were used for the steam reforming of ethanol to produce hydrogen. Co ions could enter the CeO2 lattices to form Ce1-xCoxO2-y mixed oxides at x 0.2 using the homogeneous precipitation (hp) method. CeO2 was an excellent support for Co metal in the steam reforming of ethanol because a strong interaction between support and metal (SISM) exists in the Co/CeO2 catalysts. Because Co/CeO2 (hp) prepared by homogeneous precipitation possessed a high BET surface area and small Co metal particles, Co/CeO2 (hp) showed a higher ethanol conversion than the Co/CeO2 catalysts prepared using the co-precipitation (cp) method and the impregnation (im) method. The selectivity of CO2 over Co/CeO2 (hp) increased with increasing reaction temperature at from 573 to 673 K, and decreased with increasing reaction temperature above 673 K due to the increase of CO formation. The carbonaceous deposits formed on the catalyst surface during the reaction caused a slow deactivation in the steam reforming of ethanol over Co/CeO2 (hp). The catalytic activity of the used catalysts could be regenerated by an oxidation-reduction treatment, calcined in air at 723 K and then reduced by H-2 at 673 K.
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页数:14
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