Partial oxidation of methane to synthesis gas over Pt nanoparticles supported on nanocrystalline CeO2 catalyst

被引:53
|
作者
Singha, Rajib Kumar [1 ]
Ghosh, Shilpi [1 ]
Acharyya, Shankha Subhra [1 ]
Yadav, Aditya [1 ]
Shukla, Astha [1 ]
Sasaki, Takehiko [2 ]
Venezia, Anna Maria [3 ]
Pendem, Chandrashekar [1 ]
Bal, Rajaram [1 ]
机构
[1] CSIR Indian Inst Petr, Refining Technol Div, Nanocatalysis Area, Dehra Dun 248005, India
[2] Univ Tokyo, Dept Complex Sci & Engn, Grad Sch Frontier Sci, Kashiwa, Chiba 2778561, Japan
[3] ISMN CNR, Via Ugo La Malfa 153, I-90146 Palermo, Italy
关键词
LOW-TEMPERATURE; MECHANISTIC ORIGINS; PT/CEO2; CATALYSTS; SOLID-SOLUTION; SURFACE-AREA; CO OXIDATION; CERIA; SYNGAS; NICKEL; OXIDE;
D O I
10.1039/c5cy02088c
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
Pt-nanoparticles supported on CeO2 have been prepared by a post synthesis method (Pt-CeO2PS). In the post synthesis method, CeO2 nanoparticles were prepared by a hydrothermal method, followed by the deposition of Pt nanoparticles over the CeO2. The prepared catalyst was characterized by XRD, BET-surface area, TPR, SEM, TEM, XPS and XAFS. It was observed that the catalyst prepared by the post synthesis method contained Pt nanoparticles with sizes between 2-5 nm supported on CeO2 nanoparticles with sizes between 20-60 nm. The catalytic performance of the Pt-CeO2PS catalyst was evaluated in the partial oxidation of methane for synthesis gas production. The Pt-CeO2PS catalyst could activate methane at 350 degrees C. We believe that the nanosized Pt particles and the synergy between the Pt particles, the CeO2 nanoparticles and the presence of a strong metal-support interaction play key roles in the activation of methane at such a low temperature. Different reaction parameters, like Pt-loading, reaction temperature, space velocity, and time on stream, were studied in detail. The Pt-CeO2 PS catalyst does not deactivate till 100 h with a constant H-2/CO mole ratio of 1.9 at 800 degrees C.
引用
收藏
页码:4601 / 4615
页数:15
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