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Synthesis and Characterization of Hexamethylenediammonium Thiometallates as Precursors of MoS2 and WS2 Catalysts: In situ Activation During HDS of DBT
被引:14
作者:
Alonso-Nunez, G.
[1
]
Huirache-Acuna, R.
[2
]
Paraguay-Delgado, F.
[3
,4
]
Lumbreras, J. A.
[5
]
Garcia-Alamilla, R.
[6
]
Castillo-Mares, A.
[6
]
Romero, R.
[7
]
Somanathan, R.
[8
]
Chianelli, R. R.
[9
]
机构:
[1] Univ Nacl Autonoma Mexico, Ctr Nanociencias & Nanotecnol, Ensenada 22800, Baja California, Mexico
[2] Univ Nacl Autonoma Mexico, CFATA, Juriquilla Queretaro 76230, Mexico
[3] Ctr Invest Mat Avanzados SC, Chihuahua 31109, Mexico
[4] Natl Inst Nanotechnol, Edmonton, AB T6G 2M9, Canada
[5] Univ Istmo, Sto Domingo Tehuantepec 70760, Oaxaca, Mexico
[6] Inst Tecnol Ciudad Madero, Cd Madero 89440, Tamps, Mexico
[7] UABC, Fac Ciencias Quim, Tijuana 22390, BC, Mexico
[8] Ctr Grad & Invest ITT, Tijuana 22000, BC, Mexico
[9] Univ Texas El Paso, MRTI, El Paso, TX 79968 USA
关键词:
Aqueous solution;
Hexamethylenediammonium thiometallates;
In situ-activated;
MoS2;
WS2;
catalysts;
MOLYBDENUM SULFIDE CATALYSTS;
TETRAALKYLAMMONIUM THIOMOLYBDATES;
ELECTRONIC-STRUCTURE;
DECOMPOSITION;
AMMONIUM;
HYDRODESULFURIZATION;
DIBENZOTHIOPHENE;
THIOTUNGSTATES;
COMPLEXES;
MO3S92;
D O I:
10.1007/s10562-009-9934-x
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:
Hexamethylenediammonium thiometallate (HeDaT) of molybdenum and tungsten were synthesized using the aqueous solution method. This method improved significantly the yield of the catalysts. The HeDaT precursors were in situ activated during the hydrodesulfurization (HDS) of dibenzothiophene (DBT) generating MoS2 and WS2 catalysts. To characterize the precursors Fourier Transform Infra Red (FTIR), Ultraviolet (UV-Vis) and Nuclear Magnetic Resonance (H-1 NMR) spectroscopy techniques were used to determine their chemical structures. In addition, thermal analysis (TGA-DTA) were performed to study the fragmentation and decomposition behavior of their molecular structures. Catalysts were studied by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) which showed the shapes of the particles and the characteristic fringes of the layered MoS2 and WS2 phases, respectively. Specific surface areas were determined by the BET method with values of 5 and 19 m 2/g with type I and IV adsorption-desorption nitrogen isotherms for both catalysts. The X-ray diffraction study showed poorly crystalline catalysts with weak (002) intensity for the MoS2 and a better-defined (002) reflection for the WS2.
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页码:318 / 326
页数:9
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