Mesoporous molecular sieve MCM-41 supported Co-Mo catalyst for hydrodesulfurization of petroleum resids

被引:85
|
作者
Reddy, KM
Wei, BL
Song, CS
机构
[1] Penn State Univ, Dept Mat Sci & Engn, Fuel Sci Program, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Mat Sci & Engn, Lab Hydrocarbon Proc Chem, University Pk, PA 16802 USA
关键词
hydrodesulfurization; petroleum resid; dibenzothiophene; Co-Mo; MCM-41;
D O I
10.1016/S0920-5861(98)00155-2
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work, we explored the potential of mesoporous zeolite-supported Go-Mo catalyst for hydrodesulfurization of petroleum resids, atmospheric and vacuum resids at 350-450 degrees C under 6.9 MPa of H-2 pressure. A mesoporous molecular sieve of MCM-41 type was synthesized; which has SiO2/Al2O3 ratio of about 41. MCM-41 supported Co-Mo catalyst was prepared by co-impregnation of Co(NO3)(2). 6H(2)O and (NH4)(6)Mo7O24 followed by calcination and sulfidation. Commercial Al2O3 supported Co-Mo (criterion 344TL) and dispersed ammonium tetrathiomolybdate (ATTM) were also tested for comparison purposes. The results indicated that Co-Mo/MCM-41(H) is active for HDS, but is not as good as commercial Co-Mo/Al2O3 for desulfurization of petroleum resids, It appears that the pore size of the synthesized MCM-41 (28 Angstrom) is not large enough to convert large-sized molecules such as asphaltene present in the petroleum resids. Removing asphaltene from the resid prior to HDS has been found to improve the catalytic activity of Co-Mo/MCM-41(H). The use of ATTM is not as effective as that of Co-Mo catalysts, but is better for conversions of >540 degrees C fraction as compared to noncatalytic runs at 400-450 degrees C. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:261 / 272
页数:12
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