The negative effect of residual sodium on iron-based catalyst for Fischer-Tropsch synthesis

被引:51
|
作者
An, Xia
Wu, Baoshan
Hou, Wenjuan
Wan, Haijun
Tao, Zhichao
Li, Tingzhen
Zhang, Zhixin
Xiang, Hongwei [1 ]
Li, Yongwang
Xu, Bingfu
Yi, Fan
机构
[1] Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] Wuhan Univ, Dept Phys, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
residual sodium; Fischer-Tropsch synthesis; iron-based catalyst;
D O I
10.1016/j.molcata.2006.09.003
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 residual sodium means remaining in the catalyst if the catalyst precursor has been insufficiently washed after precipitation of Fe and Cu from their nitrate solutions with sodium carbonate. The effect of such residual sodium on the co-precipitated Fe/Cu/K/SiO2 catalyst, has been investigated in connection with the characteristics of textural properties, reduction and carburization behavior. Fischer-Tropsch synthesis (FrS) was performed in a slurry-phase continuously stirred tank reactor (CSTR). As revealed by N-2 physisorption, residual sodium acts as a textural inhibitor, resulting in bigger iron phase particle size and smaller surface area. H-2 or CO temperature-programmed reduction (TPR) indicates that residual sodium suppresses reduction of catalysts in H-2 environment and carburization in CO environment. The residual sodium also inhibits the extent of carburization during in situ reduction and poisons the FrS reaction in syngas (H-2/CO = 0.67), as demonstrated by the test of X-ray diffraction (XRD) and Mossbauer spectroscopy (MES). The FTS reaction results indicate that CO conversion decreases markedly and the product distribution shifts to lighter hydrocarbons slightly with increasing residual sodium content. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:266 / 272
页数:7
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