Deep hydrodesulfurization of 4,6-dimethydibenzothiophene over CoMoS/TiO2 catalysts: Impact of the TiO2 treatment

被引:16
作者
Roy, Teddy [1 ]
Rousseau, Julie [1 ]
Daudin, Antoine [2 ]
Pirngruber, Gerhard [2 ]
Lebeau, Benedicte [3 ]
Blin, Jean-Luc [4 ]
Brunet, Sylvette [1 ]
机构
[1] Univ Poitiers, IC2MP, CNRS, UMR 7285, F-86073 Poitiers 9, France
[2] IFP Energies Nouvelles, Rond Point Echangeur Solaize, BP 3, F-69360 Solaize, France
[3] Univ Haute Alsace UHA, IS2M, CNRS, UMR 7361, F-68093 Mulhouse, France
[4] Univ Lorraine, UMR7053, L2CM, CNRS, F-54506 Vandoeuvre Les Nancy, France
关键词
Mesoporous titania; Bronsted acidity; Hydrodesulfurization; Dismutation; Isomerization; 4,6-Dimethyldibenzothiophene; SULFUR-COMPOUNDS; GAS OIL; NIMO; DESULFURIZATION; REACTIVITIES; SPECTROSCOPY; TITANIA; PROBE; COMO;
D O I
10.1016/j.cattod.2020.05.052
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Mesostructured titania as support for the CoMoS active phase in deep hydrodesulfurization (HDS) of 4,6-dimethydibenzothiophene (4,6-DMDBT) leads to an increase of the intrinsic HDS activity and a higher selectivity for direct desulfurization (DDS) for HDS reaction in contrast with the conventional CoMoS/alumina catalyst. The temperature treatment of the mesostructured TiO2 support, modifies the catalyst's activity for the transformation of 4,6-DMDBT. The higher total and HDS activities were obtained after treatment at 380 degrees C corresponding to the higher specific surface area and to a mesostructured TiO2 material with a semi-crystalline anatase framework. Beyond 550 degrees C, the specific surface area decreases strongly corresponding to a complete crystallization of the mesopores walls into anatase structure. Moreover, the temperature under which the support is treated prior its impregnation has no impact on the selectivity of the transformation routes of the sulfur compound.
引用
收藏
页码:17 / 25
页数:9
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