Impact of variables on the naphthalene hydrogenation for the tetralin formation towards BTX production

被引:2
|
作者
Vega-Merino, Pedro Martin [1 ]
Quintana-Solorzano, Roberto [1 ]
Laredo-Sanchez, Georgina Cecilia [1 ]
Arzate-Barbosa, Elva [1 ]
Olmos-Cerda, Eli Hazel [1 ]
机构
[1] Inst Mexicano Petr, Direcc Invest Transformac Hidrocarburos, Eje Cent Lazaro Cardenas Norte 152, Mexico City 07730, DF, Mexico
关键词
light cycle oil; LCO; benzene; toluene; and xylenes; BTX; hydrogenation; tetralin; HYDRODESULFURIZATION; CATALYSTS; NITROGEN;
D O I
10.1504/IJOGCT.2020.106146
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
To achieve high naphthalene conversion and selectivity to tetralin as a first step for BTX production, experiments were carried out in a bench-scale setup processing four model mixtures with a commercial CoMo/Al2O3 catalyst at 250 degrees C-375 degrees C, 1.96-7.84 MPa, and 0.7-1.4 h(-1). Model mixtures were prepared by dissolving in n-hexadecane: naphthalene (10 wt%), dibenzothiophene (1.5 wt%) and carbazole (0.05 wt%). Without dibenzothiophene and carbazole, naphthalene conversion and selectivity to tetralin reached 95.6 and 97.2wt%, respectively at 250 degrees C, 1.96 MPa and 1.2 h(-1). With dibenzothiophene and carbazole, naphthalene conversion dropped to 38.3 wt% (selectivity to tetralin = 99.6 wt%) at the same experimental conditions. Temperature and pressure were increased to 300 degrees C and 2.94 MPa to enhance naphthalene conversion (97.4 wt%); (selectivity to tetralin = 87.0 wt%). HDS and HDN were complete yet accompanied by a loss in the catalyst activity due to deactivation by coke. [Received: December 11, 2017; Accepted: May 9, 2018]
引用
收藏
页码:504 / 517
页数:14
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