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

被引:53
作者
Maity, SK [1 ]
Ancheyta, J [1 ]
Soberanis, L [1 ]
Alonso, F [1 ]
Llanos, ME [1 ]
机构
[1] Inst Mexicano Petr, Mexico City 07730, DF, Mexico
关键词
Al2O3-TiO2; Maya crude; XRD; TPR; HDM; HDS; HDN; HDAsp; deactivation;
D O I
10.1016/S0926-860X(02)00571-9
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
Three different methods are applied to prepare alumina-titania binary mixed oxide supports. These supports are used to prepare catalysts for hydrotreating of Maya heavy crude. Sequential incipient wetness and co-impregnation techniques were employed for preparation of catalysts. Ammonium heptamolybdenum was used as precursor for MoO3. Catalysts are characterized by XRD, TPR and 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. Catalyst deactivation rate is also studied. A combined method of urea hydrolysis and pH variation is suitable to prepare bigger size of pore diameter and more pore volume support. XRD results indicate that prepared alumina-titania oxides are amorphous or very poor crystalline in nature. Very complex nature of TPR profiles is observed. Two catalysts (C and D) show very high activities and also give very good stability compared to reference catalyst. We observe an average correlation between pore diameter of catalyst with HDM and HDAsp conversions. It indicates that bigger pore diameter catalyst is suitable for removal of metals and asphaltenes, but bigger pore size is not only criterion to show good HDM activity. Total pore volume is also an important parameter in this regard. Enhancement of activities is observed on P containing catalyst. Coke is deposited on the catalyst pore mouth and it caused a drastic reduction of specific surface area of spent catalyst. Coke deposition is more on the catalyst having bigger pore diameter. We also observe that rate of V removal is higher than rate of Ni removal. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:141 / 153
页数:13
相关论文
共 30 条
[1]   COKE FORMATION ON CATALYSTS DURING THE HYDROPROCESSING OF HEAVY OILS-ALPHA [J].
ABSIHALABI, M ;
STANISLAUS, A ;
TRIMM, DL .
APPLIED CATALYSIS, 1991, 72 (02) :193-215
[2]   HYDRODEMETALATION OF NICKEL AND VANADIUM PORPHYRINS .1. INTRINSIC KINETICS [J].
AGRAWAL, R ;
WEI, J .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1984, 23 (03) :505-514
[3]  
[Anonymous], HYDROTREATING CATALY
[4]   EFFECT OF PHOSPHORUS ON THE SURFACE CONCENTRATION OF MOLYBDENUM AND NICKEL IN THE OXIDE FORM OF NICKEL MOLYBDENUM ALUMINA CATALYSTS AND ON THEIR HYDRODESULFURIZATION ACTIVITY [J].
ATANASOVA, P ;
HALACHEV, T ;
UCHYTIL, J ;
KRAUS, M .
APPLIED CATALYSIS, 1988, 38 (02) :235-240
[5]   Comparison of the performance of upflow and downflow small-reactors in hydrodesulfurization reactions [J].
Castañeda-López, LC ;
Alonso-Martínez, F ;
Ancheyta, J ;
Maity, SK ;
Rivera-Segundo, E ;
Matus-Guerra, MN .
ENERGY & FUELS, 2001, 15 (05) :1139-1144
[6]   Kinetics of resid hydrotreating reactions [J].
Chang, J ;
Liu, JS ;
Li, DD .
CATALYSIS TODAY, 1998, 43 (3-4) :233-239
[7]   Hydrodemetalation of residue oil over CoMo/alumina aluminum phosphate catalysts in a trickle bed reactor [J].
Chen, YW ;
Hsu, WC .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1997, 36 (07) :2526-2532
[8]  
EIJISBOUTS S, 1991, J CATAL, V131, P412
[9]   Deactivation of hydroprocessing catalysts [J].
Furimsky, E ;
Massoth, FE .
CATALYSIS TODAY, 1999, 52 (04) :381-495
[10]   COMMENTS ON THE HDS, HDM AND HDN ACTIVITIES OF COMMERCIAL CATALYSTS IN THE HYDROTREATING OF HEAVY CRUDE OILS [J].
GAJARDO, P ;
PAZOS, JM ;
SALAZARGUILLEN, A .
APPLIED CATALYSIS, 1982, 2 (4-5) :303-313