Co promotion of sonochemically prepared MoS2/Al2O3 by impregnation with Co(acac)2•2H2O

被引:4
|
作者
Lee, Sang Il [1 ,2 ]
Cho, Ara [1 ,2 ]
Koh, Jae Hyun [3 ]
Oh, Seung Hoon [3 ]
Moon, Sang Heup [1 ,2 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[2] Seoul Natl Univ, Inst Chem Proc, Seoul 151744, South Korea
[3] SK Energy Co Ltd, Inst Technol, Taejon 305712, South Korea
关键词
Hydrodesulfurization; CoMo; Sonochemical synthesis; Co-acetylacetonate; Dibenzothiophene; 4,6-Dimethyldibenzothiophene; VAPOR-DEPOSITION METHODS; HYDRODESULFURIZATION CATALYSTS; DEEP DESULFURIZATION; ACTIVE-SITES; DIBENZOTHIOPHENE; ALKYLDIBENZOTHIOPHENES; PERFORMANCE; SUPPORT; OIL;
D O I
10.1016/j.apcatb.2010.09.025
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
A highly active CoMoS/Al2O3 catalyst was prepared by sonochemically synthesizing MoS2 crystallites dispersed on Al2O3 and subsequently impregnating the prepared MoS2/Al2O3 with Co(acac)(2)center dot 2H(2)O. The formation of the catalytically active CoMoS phase was promoted when Co(acac)(2)center dot 2H(2)O, instead of relatively common Co(NO3)(2)center dot 6H(2)O, was used as a Co precursor. As a result, the newly prepared catalyst exhibited about two times higher activity for the hydrodesulfurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT) than in the case of a catalyst prepared by the sonochemical synthesis of MoS2/Al2O3 followed by impregnation with Co(NO3)(2)center dot 6H(2)O, and even about four times higher than the activity of a catalyst prepared by sequential impregnation with Mo and Co compounds. The newly prepared catalyst enhanced the direct desulfurization (DDS) route to a greater extent than the hydrogenation route (HYD). (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:220 / 225
页数:6
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