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Highly Active Sm2O3-Ni Xerogel Catalysts for CO2 Methanation

机译:高活性SM2O3-Ni Xerogel催化剂用于CO2甲烷化

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摘要

We report on a new synthesis route for pure Sm2O3 andSm(2)O(3)-Ni xerogels by modifying the well-known epoxide addition method. The resulting xerogels are used to prove the suitability of samaria as a highly effective catalyst support and to determine the optimal Ni loading. Therefore, a set of five catalysts with Ni loadings between 4 wt% and 89 wt% Ni was prepared and fully characterized by X-ray diffraction, N-2 physisorption, transmission electron microscopy and H-2 temperature-programmed reduction. Catalytic measurements reveal that the catalyst with 39 wt% Ni shows the best catalytic performance, outperforming even highly active literature known systems. Stability runs indicate that the catalyst deactivates independently of the Ni loading as well as conversion level over 600 min due to, most likely, carbonate formation. This deactivation, however, is reversible by a simple regeneration step. As shown by simultaneous CO2/CO methanation measurements, the Ni-Sm2O3 catalysts are also highly efficient for CO methanation. In this case, CO is preferentially converted to methane compared to CO2.
机译:通过改变众所周知的环氧化物添加方法,我们报告纯SM2O3和SM(2)O(3)-NI Xerogels的新合成路线。所得到的Xerogels用于证明撒玛利亚作为高效催化剂载体的适用性,并确定最佳Ni负荷。因此,通过X射线衍射,N-2物理吸附,透射电子显微镜和H-2温度编程,制备一组具有4wt%和89wt%Ni的Ni载荷,其具有4wt%和89wt%Ni的催化剂,并用X射线衍射,N-2物理吸附,透射电子显微镜和H-2温度减小。催化测量表明,具有39wt%Ni的催化剂显示出最佳的催化性能,甚至优于高活性文献已知的系统。稳定性运行表明催化剂由于最可能碳酸盐的形成,催化剂独立于Ni负载和600分钟的转化水平停用。然而,这种停用是通过简单的再生步骤来回可逆的。如同时CO 2 / CO甲烷化测量所示,Ni-SM2O3催化剂也具有高效的CO甲烷化。在这种情况下,与CO 2相比,CO优先转化为甲烷。

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