High Metal-Acid Balance and Selective Hydrogenation Activity Catalysts for Hydrocracking of 1-Methylnaphthalene to Benzene, Toluene, and Xylene

被引:29
作者
Wu, Tao [1 ,2 ,3 ]
Chen, Sheng-Li [1 ,2 ]
Yuan, Gui-mei [1 ,4 ]
Pan, Xuejun [3 ]
Du, Jianan [1 ,2 ]
Zhang, Yanting [1 ,2 ]
Zhang, Nini [1 ,2 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] China Univ Petr, Dept Chem Engn & Environm, Beijing 102249, Peoples R China
[3] Univ Wisconsin, Dept Biol Syst Engn, Madison, WI 53706 USA
[4] China Univ Petr, Dept Sci, Beijing 102249, Peoples R China
关键词
LIGHT CYCLE OIL; DEPOSITION-PRECIPITATION; GAS OIL; HYDRODESULFURIZATION; DIBENZOTHIOPHENE; PERFORMANCE;
D O I
10.1021/acs.iecr.9b06158
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Hydrocracking of 1-methylnaphthalene to benzene (B), toluene (T), and xylene (X) was performed over a series of bi-functional catalysts (W/Beta) at 420 degrees C and 6 MPa. The reaction results and kinetic study indicated that metal-acid balance (metal-acid interaction and metal-acid ratio) and metal dispersion had a great impact on the cracking, hydrogenation, and selective hydrogenation activity, which directly determine the BTX yield. An inappropriate metal-acid ratio would lead to producing plenty of intermediates or by-products, and poor metal dispersion would result in low hydrogenation activity. However, good metal dispersion usually accompanies the strong metal-acid interaction, which reduces the sulfidation of metal. In this work, a new tungsten precursor, W-complex, was used to prepare the catalysts with good dispersion of metal oxides and high hydrogenation activity. The external surface acidity of zeolite was modified to regulate the metal-acid interaction by forming a layer of SiO2 on acid sites through chemical liquid deposition.
引用
收藏
页码:5546 / 5556
页数:11
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