Alumina-silica binary mixed oxide used as support of catalysts for hydrotreating of Maya heavy crude

被引:33
作者
Maity, SK [1 ]
Ancheyta, J [1 ]
Soberanis, L [1 ]
Alonso, F [1 ]
机构
[1] Inst Mexicano Petr, Mexico City 07730, DF, Mexico
关键词
Al2O3-SiO2; Maya crude; TPR; hydrotreating; deactivation;
D O I
10.1016/S0926-860X(03)00292-8
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
Alumina-silica binary mixed oxide support is used to prepare catalysts for hydrotreating of Maya heavy crude. Support is prepared by urea hydrolysis. Sequential incipient wetness and co-impregnation techniques are employed for preparation of catalysts. Ammonium heptamolybdenum is used as precursor of MoO3. Catalysts are characterized by X-ray diffraction (XRD), temperature-programmed reduction (TPR) and the pore size distribution. Hydrodemetallation (HDM), hydrodesulfurization (HDS), hydrodenitrogenation (HDN), and asphaltene conversion (HDAsp) reactions are studied on these catalysts. One reference catalyst is also taken for comparison. Coke and metals depositions on spent catalysts are measured. The catalyst deactivation rate is also studied. The X-ray diffraction (XRD) results reveal that molybdenum atoms are well dispersed into CoMo catalyst, whereas MoO3 crystalline phases are found in PCoMo and PNiMo catalysts. TPR reduction profiles are different for different catalysts. The laboratory made catalyst is reduced at one temperature, whereas the reference catalyst shows two reduction profiles. The reference catalyst shows the highest activities among four catalysts. The highest HDM and HDAsp activities of the reference catalyst may be due to its bigger pore diameter. The presence of TiO2 in the reference catalyst enhances HDS and HDN activities. The CoMo catalyst shows higher activities than those of PCoMo and PNiMo catalysts. The presence of crystalline MoO3 causes for lower activities of catalysts PCoMo and PNiMo. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 238
页数:8
相关论文
共 18 条
  • [1] COKE FORMATION ON CATALYSTS DURING THE HYDROPROCESSING OF HEAVY OILS-ALPHA
    ABSIHALABI, M
    STANISLAUS, A
    TRIMM, DL
    [J]. APPLIED CATALYSIS, 1991, 72 (02): : 193 - 215
  • [2] Comparison of different Ni-Mo/alumina catalysts on hydrodemetallization of Maya crude oil
    Ancheyta, J
    Maity, SK
    Betancourt-Rivera, G
    Centeno-Nolasco, G
    Rayo-Mayoral, P
    Gómez-Pérez, MT
    [J]. APPLIED CATALYSIS A-GENERAL, 2001, 216 (1-2) : 195 - 208
  • [3] [Anonymous], CATALYST DEACTIVATIO
  • [4] [Anonymous], HYDROTREATING CATALY
  • [5] CHARACTERIZATION OF SUPPORTED MOO3 BY TEMPERATURE-PROGRAMMED REDUCTION
    BRITO, J
    LAINE, J
    [J]. POLYHEDRON, 1986, 5 (1-2) : 179 - 182
  • [6] Comparison of the performance of upflow and downflow small-reactors in hydrodesulfurization reactions
    Castañeda-López, LC
    Alonso-Martínez, F
    Ancheyta, J
    Maity, SK
    Rivera-Segundo, E
    Matus-Guerra, MN
    [J]. ENERGY & FUELS, 2001, 15 (05) : 1139 - 1144
  • [7] Kinetics of resid hydrotreating reactions
    Chang, J
    Liu, JS
    Li, DD
    [J]. CATALYSIS TODAY, 1998, 43 (3-4) : 233 - 239
  • [8] Deactivation of hydroprocessing catalysts
    Furimsky, E
    Massoth, FE
    [J]. CATALYSIS TODAY, 1999, 52 (04) : 381 - 495
  • [9] COMMENTS ON THE HDS, HDM AND HDN ACTIVITIES OF COMMERCIAL CATALYSTS IN THE HYDROTREATING OF HEAVY CRUDE OILS
    GAJARDO, P
    PAZOS, JM
    SALAZARGUILLEN, A
    [J]. APPLIED CATALYSIS, 1982, 2 (4-5): : 303 - 313
  • [10] HILFMAN L, 1974, Patent No. 3825504