Effects of ZSM-5 Morphology and Fe Promoter for Dimethyl Ether Conversion to Gasoline-Range Hydrocarbons

被引:0
|
作者
Ali, Mansoor [1 ]
Kim, Jong Jin [1 ]
Zafar, Faisal [1 ]
Shen, Dongming [1 ]
Wang, Xu [1 ]
Bae, Jong Wook [1 ]
机构
[1] Sungkyunkwan Univ SKKU, Sch Chem Engn, 2066 Seobu Ro, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
conversion of dimethyl ether (DME); gasoline-range hydrocarbons; morphology of ZSM-5; Fe-modified ZSM-5; surface acidity; CATALYTIC PERFORMANCE; HIERARCHICAL ZSM-5; METHANOL SYNTHESIS; ZEOLITE CATALYSTS; BIO-SYNGAS; AROMATICS; H-ZSM-5; SELECTIVITY; MECHANISM; CUO/ZNO/AL2O3;
D O I
10.3390/catal13050910
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
The synthesis of gasoline-range hydrocarbons by gas-phase dimethyl ether (DME) conversion was investigated on various ZSM-5 zeolites with different morphologies and Fe contents. The different morphologies of ZSM-5 significantly altered the distributions of the acidic sites, which showed different selectivities to gasoline-range hydrocarbons. Nanostructured ZSM-5 (N-ZSM-5) revealed the highest C5+ selectivity of 41.7% with an aromatics selectivity of 23.6% at similar to 100% DME conversion. The superior catalytic activity of N-ZSM-5 was attributed to the largest strong Bronsted acidic sites and smaller crystallite sizes, which were beneficial for the faster removal rate of heavy hydrocarbons due to its shorter diffusion pathlength compared to conventional ZSM-5 (C-ZSM-5). In addition, 10 wt% Fe-impregnated N-ZSM-5 revealed an enhanced C5+ selectivity of 60.6% with a smaller C-1-C-4 selectivity of 21.9%, which were attributed to the adjusted acidic sites by suppressing the cracking reactions of the surface intermediates, which are responsible for the selective formation of smaller light hydrocarbons. However, the excess amount of Fe on N-ZSM-5 showed a lower DME conversion of 83.5% with a lower C5+ selectivity of 38.5% due to the blockages of the active acidic sites. Nanostructured N-ZSM-5 possessing a larger amount of strong Bronsted acid sites with 10 wt% Fe modification clearly showed a higher formation rate of gasoline-range hydrocarbons due to an enhanced secondary oligomerization of surface intermediates to form heavier aromatic hydrocarbons.
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页数:14
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