Decomposition of molybdate-hexamethylenetetramine complex: One single source route for different catalytic materials

被引:23
作者
Chouzier, Sandra [1 ]
Czeri, Tivadar [2 ]
Roy-Auberger, Magalie [2 ]
Pichon, Christophe [2 ]
Geantet, Christophe [1 ]
Vrinat, Michel [1 ]
Afanasiev, Pavel [1 ]
机构
[1] Univ Lyon 1, CNRS, Inst Rech Catalyse & Environm Lyon UMR5256, F-69626 Villeurbanne, France
[2] IFP Energies Nouvelles, F-69390 Vernaison, France
关键词
Molybdenum; Nitride; Sulfide; Catalyst; Hexamethylenetetramine; SUPPORTED MOLYBDENUM CARBIDE; RAY-ABSORPTION-SPECTROSCOPY; HYDROTREATING CATALYST; BENZENE HYDROGENATION; AMMONIA-SYNTHESIS; REDUCTION ROUTE; METAL NITRIDES; SURFACE-AREA; HYDRODESULFURIZATION; ALUMINA;
D O I
10.1016/j.jssc.2011.08.005
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Decomposition of ammonium heptamolybdate-hexamethylentetramine (HMTA) complex (HMTA)(2)(NH(4))(4)Mo(7)O(24)center dot 2H(2)O was studied as a function of treatment conditions in the range 300-1173 K. The evolution of solid products during decomposition was studied by thermal analysis and in situ EXAFS. Depending on the nature of the gas used for treatment, single phases of highly dispersed nitrides Mo(2)N, carbide Mo(2)C, or oxide MoO(2) can be obtained. The nature of the products obtained was explained by qualitative thermodynamical considerations. Morphology of the solids considerably depends on such preparation parameters as temperature and mass velocity of the gas flow. For the nitride-based materials, catalytic activity was evaluated in the model thiophene HDS reaction. It was demonstrated that NH(3)-treated samples showed better catalytic activity than N(2)-treated ones due to cleaner surface and better morphology. Transmission microscopy, XRD and XPS studies showed that MoS(2) is formed on the surface during HDS reaction or sulfidation with H(2)S. Optimized nitride-derived catalysts showed mass activity several times higher than unsupported MoS(2) or MoS(2)/Al(2)O(3) reference catalyst. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:2668 / 2677
页数:10
相关论文
共 40 条
[1]   New single source route to the molybdenum nitride Mo2N [J].
Afanasiev, P .
INORGANIC CHEMISTRY, 2002, 41 (21) :5317-5319
[2]   Nickel and cobalt hexamethylentetramine complexes (NO3)2Me(H2O)6(HMTA)2•4H2O(Me = CO2+, Ni2+):: New molecular precursors for the preparation of metal dispersions [J].
Afanasiev, Pavel ;
Chouzier, Sandra ;
Czeri, Tivadar ;
Pilet, Guillaume ;
Pichon, Christophe ;
Roy, Magalie ;
Vrinat, Michel .
INORGANIC CHEMISTRY, 2008, 47 (07) :2303-2311
[3]   Synthetic approaches to the molybdenum sulfide materials [J].
Afanasiev, Pavel .
COMPTES RENDUS CHIMIE, 2008, 11 (1-2) :159-182
[4]  
Ankudinov A.L., 2002, Phys. Rev. B, V65, P104
[5]   Influence of the degree of carburization on the density of sites and hydrogenating activity of molybdenum carbides [J].
Choi, JS ;
Bugli, G ;
Djéga-Mariadassou, G .
JOURNAL OF CATALYSIS, 2000, 193 (02) :238-247
[6]  
CHOUZIER S, 2006, PREP AM CHEM SOC DIV, V51, P285
[7]   One-step synthesis of dispersed bimetallic carbides and nitrides from transition metals hexamethylenetetramine complexes [J].
Chouzier, Sandra ;
Afanasiev, Pavel ;
Vrinat, Michel ;
Cseri, Tivadar ;
Roy-Auberger, Magalie .
JOURNAL OF SOLID STATE CHEMISTRY, 2006, 179 (11) :3314-3323
[8]   HDS and HDN activity of (Ni,Co)Mo binary and ternary nitrides prepared by decomposition of hexamethylenetetramine complexes [J].
Chouzier, Sandra ;
Vrinat, Michel ;
Cseri, Tivadar ;
Roy-Auberger, Magalie ;
Afanasiev, Pavel .
APPLIED CATALYSIS A-GENERAL, 2011, 400 (1-2) :82-90
[9]   Tetralin hydrogenation catalyzed by Mo2C/Al2O3 and WC/Al2O3 in the presence of H2S [J].
Da Costa, P ;
Lemberton, JL ;
Potvin, C ;
Manoli, JM ;
Perot, G ;
Breysse, M ;
Djega-Mariadassou, G .
CATALYSIS TODAY, 2001, 65 (2-4) :195-200
[10]   Toluene hydrogenation at low temperature using a molybdenum carbide catalyst [J].
Frauwallner, Maria-Laura ;
Lopez-Linares, Francisco ;
Lara-Romero, J. ;
Scott, Carlos E. ;
Ali, Vieman ;
Hernandez, Eumir ;
Pereira-Almao, Pedro .
APPLIED CATALYSIS A-GENERAL, 2011, 394 (1-2) :62-70