作为催化剂载体的水合钛酸钠离子交换材料的研究

B. Bunker, C. Peden, S. L. Martinez, K. M. Kimball
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引用次数: 2

摘要

了解催化剂的活性与催化剂载体上活性金属的浓度和分散之间的关系,对于设计具有最佳催化性能的材料至关重要。我们开发了控制镍在水合钛酸钠催化剂载体上的浓度和分散的合成技术。该技术要求理解支撑材料和溶解金属(水解产物)的溶液化学。在本文中,我们介绍了三个负载镍的水合钛酸钠样品的研究结果,其中镍的分散范围从原子水平到大(50纳米)簇的规模。通过透射电子显微镜(TEM)、氢化学吸附和BET表面积测量对催化剂进行了表征。此外,还利用Ni催化剂的活性和选择性来监测催化剂中Ni的表面结构。八。参考文献, 7个无花果。, 1页。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies of hydrous sodium titanate ion-exchange materials for use as catalyst supports
Understanding how the activity of a catalyst is related to the concentration and dispersion of active metals on the catalyst support is critical to designing materials having the optimum catalytic properties. We have developed synthetic techniques for controlling both the concentration and dispersion of nickel on hydrous sodium titanate catalyst supports. The techniques require an understanding of the solution chemistry of both the support material and dissolved metal species (hydrolysis products). In this paper, we present the results of a study of three nickel-loaded samples of hydrous sodium titanate in which the scale of the nickel dispersion ranges from the atomic level to the scale of large (50 nm) clusters. The catalysts are characterized by transmission electron microscopy (TEM), hydrogen chemisorption, and BET surface area measurements. In addition, the activity and selectivity of the Ni catalysts for the n-butane hydrogenolysis reaction is used to monitor the surface structures of Ni in the catalysts. 8 refs., 7 figs., 1 tab.
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