Deactivation by coke deposition on the HZSM-5 catalysts in the methanol-to-hydrocarbon conversion

被引:37
作者
Lee, Ki-Yong [1 ]
Kang, Min-Young [1 ]
Ihm, Son-Ki [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
关键词
Inorganic compounds; Microporous materials; Chemical synthesis; ZEOLITE ZSM-5; MESOPOROSITY; SELECTIVITY; PROPYLENE; STABILITY; H-ZSM-5; ACIDITY; SHAPE;
D O I
10.1016/j.jpcs.2012.09.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
HZSM-5 used to be the main catalyst component for the MTG process of Exxonmobil Co. Catalyst deactivation by coke in methanol-to-hydrocarbon (MTH) over HZSM-5 was studied in a fixed-bed reactor by observing the activity and selectivity with time-on-stream at 500 degrees C and WHSV=4.25 h(-1). The HZSM-5 with SiO2/Al2O3 ratios of 40 and 280 were synthesized and characterized with XRD. N-2 adsorption/desorption and NH3-TPD. The used catalysts were investigated by N-2 adsorption/desorption, XRD, elemental analysis (EA) and UV-vis spectroscopy to identify the nature of coke. If the acidity of HZSM-5 is low (SiO2/Al2O3=280), the coke deposited is mainly mono- or bi-aromatic which did not affect the catalyst activity significantly. On the other hand when the acidity is high (SiO2/Al2O3=40), the coke deposited is polycyclic aromatics with 3 or 4 fused rings which leads to significant deactivation after 24 h. It is presumed that the coke on the HZSM-5 with low acidity must be located inside the pores and/or in the framework, since the coke particles without polycyclic aromatics should be small. The deactivation of HZSM-5 with high acidity is mainly caused by the bulky coke molecules, most probably inducing the topological blocking of the zeolite pores and channels. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1542 / 1545
页数:4
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