Enhanced reactivity and stability in methane dehydro-aromatization over Mo/HZSM-5 physically mixed with NiO

被引:31
作者
Nam, Kihun [1 ]
Ryu, Hae Won [1 ]
Gim, Min Yeong [1 ]
Kim, Do Heui [1 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
Methane dehydro-aromatization; Mo; HZSM-5; NiO; Physical mixing; Carbon nanotube; OXYGEN-FREE CONVERSION; NATURAL-GAS; CARBON NANOTUBES; CATALYTIC STABILITY; NONOXIDATIVE CONVERSION; RAMAN-SPECTROSCOPY; ACID SITES; DEHYDROAROMATIZATION; MO; FE;
D O I
10.1016/j.apcatb.2021.120377
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
While Mo/HZSM-5 is known as a catalyst for methane dehydro-aromatization (MDA), low activity and rapid deactivation have been considered issues to be overcome. In order to improve catalytic performance, NiO was physically mixed with Mo/HZSM-5, which significantly enhanced the yield for aromatic compounds (benzene and toluene), and improved catalytic stability. Combined XRD, CH4-TPSR, CO chemisorption, TEM-EDS, NH3-TPD, pyridine FT-IR, TPO, visible Raman, and N2 physisorption analysis confirmed that NiO promoted the dispersion of MoCx active sites and suppressed coke formation on MoCx, by converting coke precursors to carbon nanotube (CNT) on itself. As a result, after the reaction, the pore size and pore volume did not change much, which is attributed to the improved stability. This study demonstrates that physically mixed NiO can act as an excellent catalyst promotor for MDA.
引用
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页数:12
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