Rational Design of Nickel Phosphide Hydrodesulfurization Catalysts: Controlling Particle Size and Preventing Sintering

被引:85
作者
Savithra, Galbokka H. Layan [1 ]
Muthuswamy, Elayaraja [1 ]
Bowker, Richard H. [2 ]
Carrillo, Bo A. [2 ]
Bussell, Mark E. [2 ]
Brock, Stephanie L. [1 ]
机构
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
[2] Western Washington Univ, Dept Chem, Bellingham, WA 98225 USA
基金
美国国家科学基金会;
关键词
Ni2P nanoparticles; hydrodesulfurization; supported catalyst; sintering; mesoporous silica shell; THIOPHENE HYDRODESULFURIZATION; METAL PHOSPHIDES; NANOPARTICLES; PHOSPHORUS; REDUCTION; GROWTH;
D O I
10.1021/cm302680j
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 size-dependent catalytic activity of Ni2P for hydrodesulfurization (HDS) remains unstudied because the traditional temperature programmed reduction (TPR) method used in catalyst preparation results in highly polydisperse Ni2P particles. The ability to control the Ni2P particle size in the range 5-20 nm by varying the quantity of oleylamine in solution-phase arrested precipitation reactions is reported. Particles were introduced to a high surface area silica support (Cab-O-Sil, M-7D grade, 200 m(2)/g) via incipient wetness, and HDS activity was probed against dibenzothiophene (DBT). All samples were less active than TPR prepared materials, and the smallest particles were the least active, contrary to expectation. This is attributed in part to particle sintering under HDS conditions. Sintering occurs independently of wt% loading of catalyst, time, incipient wetness procedure, and ionic additives, at all temperatures greater than 200 degrees C. Sintering is minimized by encapsulation of Ni2P nanoparticles in a mesoporous silica shell, achieved by sol-gel silica formation around Ni2P-containing surfactant liquid crystal assemblies and subsequent calcination, resulting in a doubling of HDS activity.
引用
收藏
页码:825 / 833
页数:9
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