A novel approach to the synthesis of unsupported nickel phosphide catalysts using nickel thiophosphate as precursor

被引:44
|
作者
Loboue, Hermione
Guillot-Deudon, Catherine [2 ]
Popa, Aurelian Florin [2 ]
Lafond, Alain [2 ]
Rebours, Bernadette [3 ]
Pichon, Christophe [3 ]
Cseri, Tivadar [3 ]
Berhault, Gilles [1 ]
Geantet, Christophe [1 ]
机构
[1] Univ Lyon 1, IRCELYON, CNRS, UMR 5256, F-69626 Villeurbanne, France
[2] Univ Nantes, Inst Mat Jean Rouxel, IMN, CNRS,UMR 6502, F-44322 Nantes, France
[3] Inst Francais Petr Lyon, F-69360 Vernaison, France
关键词
hydrodesulfurization; NiPS3; nickel phosphide; soft chemistry;
D O I
10.1016/j.cattod.2007.07.005
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Nickel thiophosphate, NiPS3 synthesized at room temperature using a soft chemistry approach (a-NiPS3) has been successfully used as precursor for low-temperature preparation of unsupported nickel phosphide. Using Raman spectroscopy and EXAFS, comparison with a wellcrystallized NiPS3 reference (c-NiPS3) first Confirmed that nickel thiophosphate can be effectively obtained at low temperatures of preparation. In situ XRD diffraction and EXAFS showed that Ni2P was obtained by the reduction of a-NiPS3 at a temperature as low as 573 K. For c-NiPS3, slower kinetics of reduction first led to the formation of an intermediate richer phosphorus-containing nickel phosphide phase, Ni5P4 at a temperature of reduction of 623 K while Ni2P started being formed at 773 K. Under hydrodesulfurization (HDS) thiophene catalytic conditions (613 K, 2.8 mol% thiophene/H-2), a-NiPS3 was decomposed into a mixture of Ni2P and Ni5P4 while c-NiPS3 was converted into Ni5P4. Both nickel phosphide catalysts exhibit much higher activities compared to a MoS2 reference. Ni5P4 exhibited a specific activity (per gram of catalyst) seven times as high as for MoS2. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 68
页数:6
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