Enhanced methane dehydroaromatization in the presence of CO2 over Fe- and Mg-modified Mo/ZSM-5

被引:29
作者
Cheng, Xu [1 ]
Yan, Peng [1 ,2 ]
Zhang, Xinzhuang [1 ,2 ]
Yang, Fan [2 ]
Dai, Chengyi [1 ]
Li, Dapeng [2 ]
Ma, Xiao-Xun [1 ]
机构
[1] Northwest Univ, Int Sci & Technol Cooperat Base Clean Utilizat Hy, Minist Educ Adv Use Technol Shanbei Energy,Sch Ch, Chem Engn Res Ctr,Minist Sci & Technol,Res Ctr En, Xian 710069, Peoples R China
[2] Yanchang Petr Grp Co Ltd, Hydrocarbon High Efficiency Utilizat Technol Res, Xian 710069, Peoples R China
基金
中国国家自然科学基金;
关键词
Mg-modified Mo/ZSM-5; Methane dehydroaromatization; CO2; co-reactants; DEHYDRO-AROMATIZATION; NONOXIDATIVE AROMATIZATION; CATALYTIC PERFORMANCE; MO/HMCM-22; CATALYSTS; ACID SITES; MAS NMR; MO/HZSM-5; OXYGEN; MOLYBDENUM; ZEOLITE;
D O I
10.1016/j.mcat.2017.05.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of metal-modified (i.e., Fe or Mg) Mo/ZSM-5 were prepared by the impregnation method and subsequently tested in the aromatization of CH4-CO2 mixtures in a continuous flow fluidized-bed quartz reactor. Mg modification improved both the catalytic activity (9.7 vs. 12.3% conversion) and the selectivity to benzene (65.7 vs. 68.4%) while inhibiting carbon deposition (13.9 vs 10.1% carbon deposited, as determined by thermogravimetry, TG) during the dehydroaromatization of methane in the presence of CO2. SEM confirmed that the carbon species deposited over Mo/HZSM-5 and Fe-Mo/HZSM-5 catalysts were mainly carbon nanotubes. In contrast, carbon nanotubes were not detected over Mg-Mo/HZSM-5. The TG profiles and the XPS spectra revealed that the introduction of Mg likely favored the generation of Mo2C species which are considered active sites for methane dehydroaromatization. The present work provides a strategy for greatly improving the catalytic performance in the methane dehydroaromatization in the presence of CO2. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:114 / 120
页数:7
相关论文
共 46 条
[1]  
Bai J, 2004, CHINESE J CATAL, V25, P70
[2]   Metastable fcc α-MoC1-x supported on HZSM5:: preparation and catalytic performance for the non-oxidative conversion of methane to aromatic compounds [J].
Bouchy, C ;
Schmidt, I ;
Anderson, JR ;
Jacobsen, CJH ;
Derouane, EG ;
Hamid, SBDA .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2000, 163 (1-2) :283-296
[3]   XPS STUDY OF THE ADHERENCE OF REFRACTORY CARBIDE, SILICIDE, AND BORIDE RF-SPUTTERED WEAR-RESISTANT COATINGS [J].
BRAINARD, WA ;
WHEELER, DR .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY, 1978, 15 (06) :1800-1805
[4]  
Cao Z., 2013, Angewandte Chemie, V125, P14039
[5]   Promotional effect of Pt on non-oxidative methane transformation over Mo-HZSM-5 catalyst [J].
Chen, LY ;
Lin, LW ;
Xu, ZS ;
Zhang, T ;
Li, XS .
CATALYSIS LETTERS, 1996, 39 (3-4) :169-172
[6]  
Dai C., 2015, ADV FUNCT MATER, V25, P13
[7]   Hollow zeolite encapsulated Ni-Pt bimetals for sintering and coking resistant dry reforming of methane [J].
Dai, Chengyi ;
Zhang, Shaohua ;
Zhang, Anfeng ;
Song, Chunshan ;
Shi, Chuan ;
Guo, Xinwen .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (32) :16461-16468
[8]   The effects of silanation of external acid sites on the structure and catalytic behavior of Mo/H-ZSM5 [J].
Ding, WP ;
Meitzner, GD ;
Iglesia, E .
JOURNAL OF CATALYSIS, 2002, 206 (01) :14-22
[9]   Identification of molybdenum oxide nanostructures on zeolites for natural gas conversion [J].
Gao, Jie ;
Zheng, Yiteng ;
Jehng, Jih-Mirn ;
Tang, Yadan ;
Wachs, Israel E. ;
Podkolzin, Simon G. .
SCIENCE, 2015, 348 (6235) :686-690
[10]   Aromatization of methane over zeolite supported molybdenum: active sites and reaction mechanism [J].
Ha, VTT ;
Tiep, LV ;
Meriaudeau, P ;
Naccache, C .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2002, 181 (1-2) :283-290