陈晨, 李海杰, 白杨, 冯富祥, 田磊, 杨勇, 刘源, 郭强. 预硫化温度对煤直接液化催化剂组分转变及其催化性能的影响[J]. 燃料化学学报(中英文), 2022, 50(1): 54-62. DOI: 10.1016/S1872-5813(21)60118-4
引用本文: 陈晨, 李海杰, 白杨, 冯富祥, 田磊, 杨勇, 刘源, 郭强. 预硫化温度对煤直接液化催化剂组分转变及其催化性能的影响[J]. 燃料化学学报(中英文), 2022, 50(1): 54-62. DOI: 10.1016/S1872-5813(21)60118-4
CHEN Chen, LI Hai-jie, BAI Yang, FENG Fu-xiang, TIAN Lei, YANG Yong, LIU Yuan, GUO Qiang. Effect of sulfidation temperature on component transformation and catalytic performance of direct coal liquefaction catalyst[J]. Journal of Fuel Chemistry and Technology, 2022, 50(1): 54-62. DOI: 10.1016/S1872-5813(21)60118-4
Citation: CHEN Chen, LI Hai-jie, BAI Yang, FENG Fu-xiang, TIAN Lei, YANG Yong, LIU Yuan, GUO Qiang. Effect of sulfidation temperature on component transformation and catalytic performance of direct coal liquefaction catalyst[J]. Journal of Fuel Chemistry and Technology, 2022, 50(1): 54-62. DOI: 10.1016/S1872-5813(21)60118-4

预硫化温度对煤直接液化催化剂组分转变及其催化性能的影响

Effect of sulfidation temperature on component transformation and catalytic performance of direct coal liquefaction catalyst

  • 摘要: 在5% H2S/N2气氛,不同预硫化温度下制备了系列硫铁催化剂,并在5 MPa 的1% H2S/H2气氛、360 ℃下研究了其催化萘的加氢活性。借助MES、XRD和XPS等表征手段,探究了催化剂在不同预硫化温度及反应条件下组分转变规律。结果表明,预硫化过程是硫由表面向内部,依照FeS2→FeS、Fe1−xS→Fe3S4→Fe2O3顺序渗硫的过程,而升高温度有利于硫向体相内的传递;接触1% H2S/H2气氛后晶粒由外向内各组分均快速转化为Fe1–xS的过程;调控预硫化条件可以实现活性组分Fe1–xS的含量高、晶粒小,于是可获得最高活性。

     

    Abstract: A series of iron sulfide catalysts were prepared in 5% H2S/N2 atmosphere at different pre-sulfidation temperatures, and their catalytic activity for naphthalene hydrogenation was studied at 360 ℃ in 1% H2S/H2 atmosphere at 5 MPa. The component transformation of the catalyst under varied pre-sulfidation temperature and reaction conditions was researched using MES, XRD and XPS. The results revealed that the sulfidation process was in the form of sulfurizing from surface to interior in the order of FeS2→FeS, Fe1–xS→Fe3S4→Fe2O3 during which transferring sulfur to the body phase was benefited from the rise of temperature. After contacting 1% H2S/H2 gas, the particles rapidly transformed to Fe1–xS from outside to the inside. By adjusting sulfidation conditions, the Fe1–xS content was high while the particle size was small, which made it possible to obtain the greatest activity of the catalyst.

     

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