School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu 225002, China.
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu 225002, China.
J Colloid Interface Sci. 2017 Nov 1;505:789-795. doi: 10.1016/j.jcis.2017.06.081. Epub 2017 Jun 24.
Ordered mesoporous carbon (OMC)-metal composites have attracted great attention owing to their combination of high surface area, controlled pore size distribution and physicochemical properties of metals. Herein, we report the cobalt nanoparticles/ordered mesoporous carbon (CoNPs@OMC) composite prepared by a one-step carbonization/reduction process assisted by a hydrothermal pre-reaction. The CoNPs@OMC composite presents a high specific surface area of 544mg, and the CoNPs are uniformly imbedded or confined in the ordered mesoporous carbon matrix. When used as a non-precious metal-containing catalyst for hydrogenation reduction of p-nitrophenol and nitrobenzene, it demonstrates high efficiency and good cycling stability. Furthermore, the CoNPs@OMC composite can be directly used to catalyze the Fischer-Tropsch synthesis for the high-pressure CO hydrogenation, and presents a good catalytic selectivity for C hydrocarbons. The excellent catalytic performance of the CoNPs@OMC composite can be ascribed to synergistic effect between the high specific surface area, mesoporous structure and well-imbedded CoNPs in the carbon matrix.
有序介孔碳(OMC)-金属复合材料因其高比表面积、可控的孔径分布和金属的物理化学性质而受到广泛关注。本文报道了一种通过水热预反应辅助的一步碳化/还原法制备的钴纳米粒子/有序介孔碳(CoNPs@OMC)复合材料。CoNPs@OMC 复合材料具有 544mg 的高比表面积,CoNPs 均匀地嵌入或限制在有序介孔碳基体中。当用作加氢还原对硝基苯酚和硝基苯的非贵金属含催化剂时,表现出高效和良好的循环稳定性。此外,CoNPs@OMC 复合材料可直接用于高压 CO 加氢的费托合成,对 C 烃具有良好的催化选择性。CoNPs@OMC 复合材料的优异催化性能可归因于高比表面积、介孔结构以及 CoNPs 在碳基质中良好的嵌入协同作用。