| 碱土及锰系复合氧化物担载Fe-K催化剂的费-托合成性能 |
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| 引用本文： | 刘振新,赵晨曦,贾高鹏,田红美,高玉集,邢宇.碱土及锰系复合氧化物担载Fe-K催化剂的费-托合成性能[J].石油学报(石油加工),2021,37(4):757-770. |
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| 作者姓名： | 刘振新 赵晨曦 贾高鹏 田红美 高玉集 邢宇 |
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| 作者单位： | 郑州轻工业大学 材料与化学工程学院 河南省表界面科学重点实验室，河南 郑州 450002 |
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| 基金项目： | 国家自然科学基金项目（21571161），河南省高等学校重点科研项目资助计划项目（20A150044）,省属高校基本科研业务费专项资金项目（19KYYWF0402），郑州轻工业大学博士科研基金项目（2016BSJJ034/CLY20170069/LZX2016），郑州轻工业大学博士单位建设财政配套资助经费项目（13308000212）资助 |
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| 摘 要： | 制备了铝氧化物(Al-O)基体分别与Mn或碱土元素构成的复合氧化物型高温钝化系列载体，担载Fe-K后制成Fe-K2O/MAl2O4 (M为Mg、Ca、Sr、Ba、Mn)催化剂，用于费-托合成反应。采用X射线粉末衍射(XRD)、电感耦合等离子体发射光谱(ICP-OES)、N2物理吸附、CO2化学吸附 程序升温脱附(CO2-TPD)、场发射电子显微镜等分析方法表征了Fe-K2O/MAl2O4催化剂的物理化学性质。采用固定床加压反应器进行了催化剂的合成气费-托转化催化性能评价。结果表明：不同元素种类(Mg、Ca、Sr、Ba、Mn)造成Fe-K2O/MAl2O4催化剂的CO2-TPD高温脱附峰面积占总脱附峰面积百分比、高温脱附峰温度等出现显著差异。对Fe-K2O/MAl2O4催化剂来说，表面碱性位的碱性越强，则催化剂的活性越高。发现所制备的5种Fe-K2O/MAl2O4催化剂的C2~C4烯/烷比、C-C偶合能力、低碳烯烃烃类选择性均与其CO2-TPD高温脱附峰温度大致呈反向关系，即当CO2-TPD高温脱附峰温度越高时，三者的数值将趋于越低。CO2-TPD高温脱附峰温度位于669～692 ℃的Fe-K2O/Mg Al2O4、Fe-K2O/MAl2O4催化剂比位于744～749 ℃的Fe-K2O/CaAl2O4、Fe-K2O/Sr Al2O4、Fe-K2O/BaAl2O4催化剂更有利于促使反应生成低碳烯烃。
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| 关 键 词： | 费-托合成 CO加氢 低碳烯烃 铁催化剂 复合氧化物 |
| 收稿时间： | 2020-06-11 |
Catalytic Performance of Fe-K Catalysts Supported on Alkaline Earth or Manganese-Containing Composite Oxides in Fischer-Tropsch Synthesis |
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| LIU Zhenxin,ZHAO Chenxi,JIA Gaopeng,TIAN Hongmei,GAO Yuji,XING Yu.Catalytic Performance of Fe-K Catalysts Supported on Alkaline Earth or Manganese-Containing Composite Oxides in Fischer-Tropsch Synthesis[J].Acta Petrolei Sinica (Petroleum Processing Section),2021,37(4):757-770. |
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| Authors: | LIU Zhenxin ZHAO Chenxi JIA Gaopeng TIAN Hongmei GAO Yuji XING Yu |
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| Affiliation: | Henen Provincial Key Laboratory of Surface and Interface Science, School of Materials and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450006, China |
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| Abstract: | A series of composite oxide type supports composed of
aluminum oxide (Al-O) matrix, manganese or alkaline earth elements were
synthesized and then passivated at high temperature. When Fe-K supported, the Fe-K2O/MAl2O4 (M=Mg, Ca, Sr, Ba, Mn) catalysts were prepared and employed by Fischer-Tropsch
(F-T) reactions. The Fe-K2O/MAl2O4 catalysts
were characterized by X-rays diffraction (XRD), inductively coupled plasma
optical emission spectrometry (ICP-OES), N2 physisorption, CO2 chemical adsorption-temperature programmed desorption (CO2-TPD), and
field emission electron microscopy. The F-T conversion of syngas was evaluated
in a fixed bed pressurized reactor to determine the performance of catalysts.
Different element (M) types cause significant differences in each percentage of
high temperature desorption peak area to total desorption peak area, as well as
the temperature of CO2-TPD high temperature desorption peaks. Strong
surface basicity favors high catalytic activity. It was determined that the C2-C4 olefin to paraffin ratio, C-C coupling ability, and the hydrocarbon selectivity
of light olefins of the five Fe-K2O/MAl2O4 catalysts
were generally contrary to the temperature of CO2-TPD high temperature
desorption peaks, that is to say, the higher the high temperature desorption
peak temperature of CO2-TPD, the lower the values of the three parameters.
The catalysts (M=Mg, Mn) with CO2-TPD high temperature desorption
peak temperature of 669-692℃ are favorable to the
production of light olefins than the catalysts (M = Ca, Sr, Ba) with desorption
peak temperature of 744-749 ℃. |
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| Keywords: | Fischer-Tropsch synthesis CO hydrogenation light olefin iron catalyst composite oxide |
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