Nanoporous gold as an active low temperature catalyst toward CO oxidation in hydrogen-rich stream

被引:0
|
作者
Li, Dongwei [1 ,2 ]
Zhu, Ye [1 ,2 ]
Wang, Hui [1 ,2 ]
Ding, Yi [1 ,2 ,3 ]
机构
[1] Shandong Univ, Ctr Adv Energy Mat & Technol Res AEMT, Jinan 250100, Peoples R China
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[3] Shandong Appl Res Ctr Gold Technol Au SDARC, Yantai 264005, Peoples R China
来源
SCIENTIFIC REPORTS | 2013年 / 3卷
基金
美国国家科学基金会; 高等学校博士学科点专项科研基金;
关键词
PREFERENTIAL OXIDATION; SELECTIVE OXIDATION; CARBON-MONOXIDE; H-2; AU; H2O; AU/ALPHA-FE2O3; DEACTIVATION; PERFORMANCE; METHANOL;
D O I
10.1038/srep03015
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Preferential CO oxidation (PROX) was investigated by using dealloyed nanoporous gold (NPG) catalyst under ambient conditions. Systematic investigations were carried out to characterize its catalytic performance by varying reaction parameters such as temperature and co-existence of CO2 and H2O, which revealed that NPG was a highly active and selective catalyst for PROX, especially at low temperature. At 20 degrees C, the exit CO concentration could be reduced to less than 2 ppm with a turnover frequency of 4.1 x 10(-2) s(-1) at a space velocity of 120,000 mL h(-1) g(cat)(-1). and its high activity could retain for more than 24 hours. The presence of residual Ag species in the structure did not seem to improve the intrinsic activity of NPG for PROX; however, they contributed to the stabilization of the NPG structure and apparent catalytic activity. These results indicated that NPG might be readily applicable for hydrogen purification in fuel cell applications.
引用
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页数:7
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