Direct conversion of synthesis gas to light olefins using dual bed reactor

被引:33
|
作者
Park, Jo-Yong [1 ,2 ]
Lee, Yun-Jo [1 ]
Jun, Ki-Won [1 ]
Bae, Jong Wook [1 ]
Viswanadham, Nagabhatla [1 ]
Kim, Young Ho [2 ]
机构
[1] KRICT, Petr Displacement Technol Res Ctr, Taejon 305600, South Korea
[2] Chungnam Natl Univ, Dept Fine Chem Engn & Appl Chem, Taejon 305764, South Korea
关键词
FT; HZSM-5; Chain termination; Selective cracking; Light olefins; Propylene; FISCHER-TROPSCH SYNTHESIS; IRON-BASED CATALYSTS; MIDDLE ISO-PARAFFINS; PD/BETA; HYDROCARBONS; ISOPARAFFINS; TEMPERATURE; CRACKING; ZSM-5; CU;
D O I
10.1016/j.jiec.2009.09.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fe-Cu-Al based FT catalyst and ZSM-5 cracking catalysts are employed in a consecutive dual bed reactor system for the production of C-2-C-4 olefins directly from synthesis gas. Effect of properties of FT and cracking catalysts on the CO conversion and product selectivity has been studied. The carburization and hydrogenation properties of catalysts related to chain propagation and termination reactions of FT catalyst are balanced by optimizing the K loading on Cu promoted Fe-Al FT catalyst. Alkalization with K resulted in the formation of Fe2O3 crystalline phase in FT catalyst, identified by XRD and this phenomenon has coincided with the suppression of chain termination reactions to yield enhanced C5+ hydrocarbons with minimum methane in synthesis gas conversion. Interestingly the olefinicity of light hydrocarbons is increased significantly after the K loading. The conceptualization of achieving higher C5+ olefinic products in FT followed by selective cracking of the C5+ into C-2-C-4 olefins has been realized by optimization of the properties of FT as well as ZSM-5 catalysts. The studies report an enthusiastic result that claims about 52% selectivity to C-2-C-4 hydrocarbon rich in olefins (77% selectivity). (C) 2009 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:847 / 853
页数:7
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