Alumina-carbon nanofiber composite as a support for MoCo catalysts in hydrodesulfurization reactions

被引:113
作者
AL-Hammadi, Saddam A. [1 ]
Al-Amer, Adnan M. [1 ]
Saleh, Tawfik A. [2 ]
机构
[1] King Fahd Univ Petr & Minerals, Dept Chem Engn, Dhahran 31261, Saudi Arabia
[2] King Fahd Univ Petr & Minerals, Dept Chem, Dhahran 31261, Saudi Arabia
关键词
CNF; Alumina; Catalysts; Dibenzothiophene; Hydrodesulfurization; HYDROTREATING CATALYSTS; DEEP DESULFURIZATION; ADSORPTIVE DESULFURIZATION; SULFIDE CATALYSTS; ACTIVATED CARBON; CHELATING-AGENTS; GAS OIL; DIBENZOTHIOPHENE; ZEOLITE; HDS;
D O I
10.1016/j.cej.2018.03.106
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Developing more effective catalysts for the hydrodesulfurization (HDS) process has gained more importance in recent decades to produce ultraclean fuel. In the current study, a novel carbon nanofiber doped alumina (AlCNF) was prepared as a support for the MoCo catalyst for the HDS reaction of dibenzothiophene (DBT). The in-situ prepared composites were characterized by using Brunauer-Emmett-Teller (BET), temperature-programmed reduction (TPR) powder X-ray diffraction (XRD), scanning electron microscope (SEM), infrared spectroscopy (FT-IR), and thermogravimetric analysis (TGA). The catalytic activity of the MoCo catalysts supported on nanofiber doped alumina (AlCNFMoCo) was tested and compared with the MoCo catalysts supported on alumina (AlMoCo). The AlCNFMoCo catalyst reduced the sulfur concentration in the liquid fuel down to below the allowed limit in a 6 h reaction time, showing a higher catalytic activity compared to AlMoCo. The improved catalytic activity of AlCNFMoCo can be explained by the high mesoporous surface area and the better dispersion of the MoCo metals on the AlCNF support compared to the alumina support. BET analysis indicated that the textural properties were improved by introducing CNF. The surface areas of AlMoCo and AlCNFMoCo were 166 and 200 m(2)/g. The SEM images indicated that the catalyst nanoparticles were well distributed on the surface of the CNF.
引用
收藏
页码:242 / 251
页数:10
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