Hu Xiu-Cui, Wang Wei-Wei, Gu Ying-Qiu, Jin Zhao, Song Qi-Sheng, Jia Chun-Jiang
Key Laboratory for Colloid and Interface Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Chempluschem. 2017 Mar;82(3):368-375. doi: 10.1002/cplu.201600444. Epub 2016 Dec 8.
High-surface-area Co-SiO nanocomposites were synthesized by a simple two-step procedure with activated carbon as the template. These materials catalyze the decomposition of ammonia to produce CO -free hydrogen. The fresh and used catalysts were characterized by various techniques including X-ray diffraction, N adsorption-desorption, and transmission electron microscopy. Furthermore, temperature-programmed reduction by hydrogen combined with the corresponding in situ XRD analysis was performed to investigate the redox properties of the as-prepared catalysts. The strong interaction between the cobalt species and silica can effectively prevent the active cobalt nanoparticles from agglomerating during calcination and the ammonia decomposition reaction. The ammonia reaction rate reached about 7000 mol NH mol h with a very high GHSV of 124 000 cm g h at 600 °C; this rate was maintained for 48 h without any observable deactivation of the as-obtained Co-SiO nanocomposite catalyst.
采用以活性炭为模板的简单两步法合成了高比表面积的Co-SiO纳米复合材料。这些材料催化氨分解以产生无CO的氢气。通过包括X射线衍射、N吸附-脱附以及透射电子显微镜在内的各种技术对新鲜催化剂和使用过的催化剂进行了表征。此外,进行了氢气程序升温还原并结合相应的原位XRD分析,以研究所制备催化剂的氧化还原性质。钴物种与二氧化硅之间的强相互作用可有效防止活性钴纳米颗粒在煅烧和氨分解反应过程中团聚。在600℃时,氨反应速率达到约7000 mol NH₃/molₓCo·h,具有124 000 cm³ g⁻¹ h⁻¹的非常高的气体时空速度;该速率在48 h内保持不变,所得到的Co-SiO纳米复合催化剂没有任何可观察到的失活现象。