Study of Dibenzothiophene Adsorption Over Carbon Nanotube Supported CoMo HDS Catalysts

来源 :Journal of Natural Gas Chemistry | 被引量 : 0次 | 上传用户:mingliqq
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Adsorption properties of dibenzothiophene (DBT) on a CNT (carbon nanotube) support as well as on CoMoS/CNT and CoMoO/CNT catalysts have been studied. Consecutive desorption of adsorbates was measured by TGA. The commonly used carriers AC (activated carbon), γ-Al_2O_3, and their supported catalysts (CoMoO/AC, CoMoS/AC, CoMoO/γ-Al_2O_3, CoMoS/γ-Al_2O_3)were also subjected to analysis for comparison. The acidic properties of the samples were characterized using the NH_3-TPD technique. Correlation between the adsorption of DBT and the acidic properties of the catalysts has been established. It was found that the Co-Mo catalysts in the sulfide state adsorbed much more DBT molecules than the corresponding Co-Mo catalysts in the oxide state. The CoMoS/CNT catalyst exhibited very high HDS activity and selectivity, as compared with the CoMoS/γ-Al)_2O_3 catalysts. Based on the BET data and the high hydrogenolysis/hydrogenation selectivity of the CoMoS/CNT, it was deduced that more than 90% of the DBT molecules Adsorption properties of dibenzothiophene (DBT) on a CNT (carbon nanotube) support as well as CoMoS / CNT and CoMoO / CNT catalysts have been studied. Consecutive desorption of adsorbates was measured by TGA. The commonly used carriers AC (activated carbon) The acidic properties of the samples were characterized using the NH 3-TPD (CoMoO / AC, CoMoS / AC, CoMoO / γ- Al 2 O 3, CoMoS / Correlation between the adsorption of DBT and the acidic properties of the catalysts has been established. It was found that the Co-Mo catalysts in the sulfide state adsorbed much more DBT molecules than the corresponding Co-Mo catalysts in the oxide state. Based on the BET data and the high hydrogenolysis / hydrogenation selectivity of the CoMoS / CNT, it was deduced that the more than 90% CoMoS / CNT catalyst was very high HDS activity and selectivity, as compared with the CoMoS / γ- % o f the DBT molecules
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