Development of a Ni-Pd/CeZrO2/Al2O3 Catalyst for the Effective Conversion of Methane into Hydrogen-Containing Gas

被引:16
|
作者
Kerzhentsev, M. A. [1 ]
Matus, E. V. [1 ]
Rundau, I. A. [1 ,2 ]
Kuznetsov, V. V. [1 ]
Ismagilov, I. Z. [1 ]
Ushakov, V. A. [1 ]
Yashnik, S. A. [1 ]
Ismagilov, Z. R. [1 ,3 ]
机构
[1] Russian Acad Sci, Boreskov Inst Catalysis, Siberian Branch, Novosibirsk 630090, Russia
[2] Novosibirsk State Tech Univ, Novosibirsk 630073, Russia
[3] Russian Acad Sci, Inst Coal Chem & Chem Mat Sci, Siberian Branch, Kemerovo 650000, Russia
关键词
Ni-Pd catalysts; aluminum oxide; autothermal reforming; methane; hydrogen; NI CATALYSTS; NI/MG(AL)O CATALYSTS; STEAM; PD; RH; PERFORMANCE; ECONOMY; FUTURE; FUEL;
D O I
10.1134/S002315841705010X
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
The effects of the Pd content (0-1 wt %) and the synthesis method (joint impregnation with Ni + Pd and Pd/Ni or Ni/Pd sequential impregnation) on the physicochemical and catalytic properties of Ni-Pd/CeZrO2/Al2O3 were studied in order to develop an efficient catalyst for the conversion of methane into hydrogen-containing gas. It was shown that variation in the palladium content and a change in the method used for the introduction of an active constituent into the support matrix make it possible to regulate the redox properties of nickel cations but do not affect the size of NiO particles (14.0 +/- 0.5 nm) and the phase composition of the catalyst ((gamma + delta)-Al2O3, CeZrO2 solid solution, and NiO). It was established that the activity of Ni-Pd catalysts in the reaction of autothermal methane reforming depends on the method of synthesis and increases in the following order: Ni + Pd < Ni/Pd < Pd/Ni. It was found that, as the Pd content of the Ni-Pd/CeZrO2/Al2O3 catalyst was decreased from 1 to 0.05 wt %, the ability for self-activation, high activity, and operational stability of the catalyst under the conditions of autothermal methane reforming remained unaffected: at 850 degrees C, the yield of hydrogen was similar to 70% at a methane conversion of similar to 100% during a 24-h reaction.
引用
收藏
页码:601 / 609
页数:9
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