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Direct production of olefins via syngas conversion over Co2C-based catalyst in slurry bed reactor

机译:在浆床反应器中通过基于Co2C的催化剂上的合成气转化直接生产烯烃

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Direct production of olefins via syngas conversion over a Co _(2) C-based catalyst was investigated in a slurry bed reactor (SBR). It was found that the total selectivities to olefins and oxygenates reached 88.8C% at a CO conversion of 29.5% at 250?°C, 5 bar and H _(2) /CO = 0.5. The hydrocarbon distribution greatly deviated from the classical Anderson–Schulz–Flory (ASF) distribution, with only 2.6C% methane selectivity was obtained. XRD and TEM characterization verified that the Co _(2) C nanoprisms with special exposed facts of (101) and (020) constitutes the Fischer–Tropsch to olefins (FTO) active site. The catalytic activity increased gradually with rising the reaction temperature, while the product distribution almost kept unchanged under various reaction condition in SBR. Compared to the reaction in FBR, the Co _(2) C-based catalyst exhibited relative better catalytic performance during FTO process in SBR. Specifically, a higher CO conversion, a lower methane selectivity and a higher total selectivities to olefins and oxygenates were achieved in SBR. In addition, the catalyst can be in situ reduced in slurry bed reactor at mild temperature (300 °C) and no obvious deactivation was found within nearly 100 h time-on-stream, which suggested a promising route for the direct production of olefins via syngas in industrial application.
机译:在淤浆床反应器(SBR)中研究了通过Co_(2)C基催化剂通过合成气转化直接生产烯烃的方法。发现在250℃,5巴和H _(2)/CO=0.5下,在29.5%的CO转化率下,对烯烃和含氧化合物的总选择性达到了88.8%。碳氢化合物的分布大大偏离了经典的安德森-舒尔茨-弗洛里(ASF)分布,仅获得2.6C%的甲烷选择性。 XRD和TEM表征证明,具有特殊暴露事实(101)和(020)的Co _(2)C纳米棱镜构成了费托烯烃合成(FTO)活性位点。随着反应温度的升高,催化活性逐渐提高,而在各种反应条件下,丁苯橡胶中产物的分布几乎保持不变。与FBR中的反应相比,Co_(2)C基催化剂在SBR中的FTO过程中表现出相对更好的催化性能。特别地,在SBR中获得了更高的CO转化率,更低的甲烷选择性以及对烯烃和含氧化合物的更高的总选择性。此外,可以在温和的温度下(300°C)在淤浆床反应器中原位还原催化剂,并且在近100小时的运行时间内未发现明显的失活现象,这为通过碳氢化合物直接生产烯烃提供了有希望的途径合成气在工业上的应用。

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