Liu Yang, Wu Dongshuang, Yu Fei, Yang Ruoou, Zhang Hao, Sun Fanfei, Zhong Liangshu, Jiang Zheng
Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201800, China and Shanghai Synchrotron Radiation Facility, Zhangjiang National Lab, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201204, China.
Division of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502, Japan.
Phys Chem Chem Phys. 2019 May 28;21(20):10791-10797. doi: 10.1039/c9cp01298b. Epub 2019 May 14.
Fischer-Tropsch (F-T) synthesis is an effective approach to convert the syngas of H and CO into lower olefin and other valuable products for the chemical industry. Cobalt carbide (CoC), which was regarded as the sign of activity loss in the past, has recently been recognized as a highly-active phase for F-T synthesis. However, systematic study on the formation process of CoC by F-T reaction is still lacking. Herein, for the first time, in situ XAFS (X-ray Absorption Fine Structure) experiments were conducted to elaborate the CoC formation under operando conditions. F-T reaction processes starting from Co and CoO were analysed with the conclusion that CoC could be formed under both conditions. For the CoO process, CoC was transformed directly from CoO as a wavelet transform and EXAFS fitting results revealed that there was no sign of Co metal in the whole process. Thermodynamic analysis indicated that the ΔG value of the CoO process is much smaller than that of the Co process, which means that CoO is thermodynamically easier to transform to CoC. Combining with the shorter reduction time from CoO to CoO, it can be concluded that CoO is more favourable as the precursor to synthesize CoC, which might be applied to the F-T industry. Besides, catalytic evaluation shows that the CO selectivity, CO conversion and the ratio of olefin/paraffin for the CoO process are different from those of the Co process. In addition, the reaction temperatures were also investigated wherein CoC would be partially transformed to metallic Co when the temperature was increased up to 270 °C. This work provides fundamental and applicable guidance towards the synthesis of CoC by F-T reaction.
费托(F-T)合成是一种将H和CO合成气转化为低级烯烃及其他化工行业有价值产品的有效方法。碳化钴(CoC)过去被视为活性损失的标志,最近却被认为是费托合成的高活性相。然而,目前仍缺乏对费托反应生成CoC过程的系统研究。在此,首次进行了原位X射线吸收精细结构(XAFS)实验,以阐述在操作条件下CoC的形成过程。分析了从Co和CoO开始的费托反应过程,得出在两种条件下均可形成CoC的结论。对于CoO过程,CoC直接由CoO转化而来,小波变换和扩展X射线吸收精细结构(EXAFS)拟合结果表明,整个过程中没有Co金属的迹象。热力学分析表明,CoO过程的ΔG值远小于Co过程,这意味着CoO在热力学上更容易转化为CoC。结合从CoO到CoC更短的还原时间,可以得出结论,CoO作为合成CoC的前驱体更有利,这可能应用于费托工业。此外,催化评价表明,CoO过程的CO选择性、CO转化率以及烯烃/石蜡比与Co过程不同。此外,还研究了反应温度,当温度升至270℃时,CoC会部分转化为金属Co。这项工作为通过费托反应合成CoC提供了基础且实用的指导。