Nanoparticle Growth in Supported Nickel Catalysts during Methanation Reaction-Larger is Better

被引:98
|
作者
Munnik, Peter [1 ]
Velthoen, Marjolein E. Z. [1 ]
de Jongh, Petra E. [1 ]
de Jong, Krijn P. [1 ]
Gommes, Cedric J. [2 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, NL-3584 CG Utrecht, Netherlands
[2] Univ Liege, Dept Chem Engn, B-4000 Liege, Belgium
关键词
crystal growth; heterogeneous catalysis; nanoparticles; nickel; supported catalysts; FISCHER-TROPSCH CATALYSTS; CO HYDROGENATION; PARTICLE-SIZE; THERMAL-DECOMPOSITION; KINETICS; CARBONYL; TEMPERATURE; REDUCTION; PLATINUM; SURFACES;
D O I
10.1002/anie.201404103
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A major cause of supported metal catalyst deactivation is particle growth by Ostwald ripening. Nickel catalysts, used in the methanation reaction, may suffer greatly from this through the formation of [Ni(CO)(4)]. By analyzing catalysts with various particle sizes and spatial distributions, the interparticle distance was found to have little effect on the stability, because formation and decomposition of nickel carbonyl rather than diffusion was rate limiting. Small particles (3-4 nm) were found to grow very large (20-200 nm), involving local destruction of the support, which was detrimental to the catalyst stability. However, medium sized particles (8 nm) remained confined by the pores of the support displaying enhanced stability, and an activity 3 times higher than initially small particles after 150 h. Physical modeling suggests that the higher [Ni(CO)(4)] supersaturation in catalysts with smaller particles enabled them to overcome the mechanical resistance of the support. Understanding the interplay of particle size and support properties related to the stability of nanoparticles offers the prospect of novel strategies to develop more stable nanostructured materials, also for applications beyond catalysis.
引用
收藏
页码:9493 / 9497
页数:5
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