Comparing the CO oxidation activity of free PdO and Pd2+ ions over PdO-CeO2/SiO2 catalysts

被引:21
|
作者
Wang, Shu-Yuan [1 ]
Li, Na [1 ]
Zhou, Ren-Mei [1 ]
Jin, Ling-Yun [1 ]
Hu, Geng-Shen [1 ]
Lu, Ji-Qing [1 ]
Luo, Meng-Fei [1 ]
机构
[1] Zhejiang Normal Univ, Inst Phys Chem, Minist Educ Adv Catalysis Mat, Key Lab, Jinhua 321004, Peoples R China
关键词
PdO-CeO2/SiO2; catalyst; CO oxidation; Active site; TOF; LOW-TEMPERATURE OXIDATION; RAMAN-SPECTROSCOPY; DOPED ALPHA-FE2O3; OXYGEN VACANCIES; SOLID-SOLUTION; X-RAY; GOLD; CEO2; CERIA; IDENTIFICATION;
D O I
10.1016/j.molcata.2013.03.019
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
Aiming at comparing the CO oxidation activity of free PdO and Pd2+ ions, a series of PdO-CeO2/SiO2 catalysts were prepared via an impregnation method and the turnover frequencies of them were quantitatively evaluated. The catalysts were further characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), temperature-programmed reduction (TPR), Raman technique and CO chemisorption. It was found that free PdO species and Pd2+ ions could be segregated efficiently by nitric acid treatment. The PdO-CeO2/SiO2 catalyst calcined at 600 degrees C showed the highest activity. The results of CO chemisorption suggested that free PdO species had a higher activity than Pd2+ ions, and the turnover frequencies of them were 3.27 x 10(-2) s(-1) and 0.49 x 10(-2) s(-1), respectively. The activity of PdO-CeO2/SiO2 catalyst was higher than that of PdO/SiO2 catalyst. Moreover, the CO catalytic activity of PdO-CeO2/SiO2 catalyst could be assigned to the synergetic effect of free PdO and Pd2+ ions, and this effect could improve the CO catalytic activity of catalysts. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 58
页数:6
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