催化作用
煅烧
钌
分解
氨
无机化学
氢
制氢
粒径
色散(光学)
氨生产
化学
金属
材料科学
化学工程
有机化学
物理化学
工程类
物理
光学
作者
M. Pinzón,Amaya Romero,A. de Lucas-Consuegra,A. Osa,Paula Sánchez
标识
DOI:10.1016/j.jiec.2020.11.003
摘要
A series of ruthenium catalysts using β-SiC as a support was synthesized with different metal loading (1−5 wt.% of Ru). Catalysts were characterized and tested with hydrogen production by catalytic ammonia decomposition. Additionally, the influence of calcination conditions as well as reduction temperatures (673 K and 873 K) was studied. Ru dispersion and metallic particle size were found to greatly influence catalytic activity. Moreover, calcination in a nitrogen atmosphere could remove a higher proportion of chlorine species derived from the precursor, thereby enhancing catalytic activity. Furthermore, a lower reduction temperature resulted in smaller particle sizes of ruthenium, which were more active in ammonia decomposition. Maximum intrinsic activity was obtained for a Ru size of around 5 nm. The catalyst containing 2.5 wt.% Ru, calcined in a N2 atmosphere and reduced at 673 K resulted in excellent H2 production from ammonia decomposition, with ammonia conversion close to 100% at 623 K was obtained. Porous SiC proved to be a suitable support for the nanosized Ru catalyst and was highly active in hydrogen production from ammonia decomposition. Moreover, this support provided good performance stability after one day of reaction.
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