催化学报 ›› 2008, Vol. 29 ›› Issue (6): 559-565.

• 研究论文 • 上一篇    下一篇

Cu-Fe基催化剂上CO加氢反应过程中物相的转化行为

林明桂1,2,房克功1,李德宝1,孙予罕1   

  1. 1 中国科学院山西煤炭化学研究所煤转化国家重点实验室, 山西太原 030001; 2 中国科学院研究生院, 北京 100049
  • 收稿日期:2008-06-25 出版日期:2008-06-25 发布日期:2012-04-28

Phase Transformation in Cu-Fe-Based Catalyst during CO Hydrogenation

LIN Minggui1,2, FANG Kegong1, LI Debao1, SUN Yuhan1*   

  1. 1 State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, The Chinese Academy of Sciences, Taiyuan 030001, Shanxi, China; 2 Graduate University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2008-06-25 Online:2008-06-25 Published:2012-04-28

摘要: 研究了Cu-Fe基催化剂上CO加氢反应过程中各组分尤其是铁的体相和表面微观结构的转化行为. 通过XRD、Mssbauer谱、XPS和Raman光谱等表征手段全程跟踪铁形态的变化. 结果表明,还原后体相的铁发生了明显的碳化,物相以Fe3O4和χ-Fe5C2为主,随着反应温度的升高, χ-Fe5C2的含量出现最大值. 而还原后催化剂表面没有检测到明显的铁的碳化. 这种表面性质与体相的差异来源于铁独特的还原方式,这种还原方式造成锌和锰等组分在催化剂表面富集. 而在反应过程中,系统中还原/氧化气氛的变化导致铁组分在催化剂表面富集. 还原后自由碳原子在催化剂表面沉积,并随着反应的进行,碳原子的形态发生变化,显著抑制了Cu和Fe之间的协同作用,削弱了Cu-Fe基催化剂的链增长能力.

关键词: 低碳醇合成, 铜-铁基催化剂, 物相转化, 一氧化碳, 加氢反应

Abstract: Phase transformation, especially the state of iron, in the Cu-Fe-based catalyst during CO hydrogenation was investigated byX-raydiffraction, Mssbauer spectroscopy,X-rayphotoelectron spectroscopy, and laser Raman spectroscopy. Fe2O3 transformed into a mixture of Fe3O4 and χ-Fe5C2 upon syngas pretreatment at 300 ℃, and the percentage of χ-Fe5C2 went through a maximum during the reaction. The exposure of the reduced catalyst to the reaction conditions clearly influenced its morphology. However, no clear carburization of iron was observed on the surface of the reduced catalyst. The obvious discrepancy was due to the unique reduction characteristic of iron, leading to the enrichment of zinc and manganese atoms on the surface. Instead, iron atoms were enriched on the surface during the CO hydrogenation, which was resulted from the change of oxidation-reduction properties. After reduction, some free carbon deposited on the catalyst surface, and their graphitization took place when the reaction was carried out at 220 ℃ and was enhanced with increasing reaction temperature. This process significantly weakened the synergistic effect between copper and iron and therefore restrained the chain growth ability of the Cu-Fe-based catalyst.

Key words: higher alcohol synthesis, copper-iron catalyst, phase transformation, carbon monoxide, hydrogenation