催化作用
活化能
纳米颗粒
产量(工程)
棒
反应级数
化学
反应机理
氧化还原
化学工程
材料科学
无机化学
结晶学
物理化学
纳米技术
动力学
反应速率常数
有机化学
冶金
物理
替代医学
病理
工程类
医学
量子力学
作者
Chenwei Li,Yu Sun,Igor Djerdj,Pascal Voepel,Christian Sack,Tobias Weller,Rüdiger Ellinghaus,Joachim Sann,Yanglong Guo,Bernd Smarsly,Herbert Over
标识
DOI:10.1021/acscatal.7b01618
摘要
CeO2 is a promising catalyst for the HCl oxidation (Deacon process) in order to recover Cl2. Employing shape-controlled CeO2 nanoparticles (cubes, octahedrons, rods) with facets of preferential orientations ((100), (111), (110)), we studied the activity and stability under two reaction conditions (harsh: Ar:HCl:O2 = 6:2:2 and mild: Ar:HCl:O2 = 7:1:2). It turns out that both activity and stability are structure-sensitive. In terms of space time yield (STY), the rods are the most active particles, followed by the cubes and finally the octahedrons. This very same trend is reconciled with the complete oxygen storage capacity (OSCc), indicating a correlation between the observed activity STY and the OSCc. The apparent activation energies are about 50 kJ/mol for cubes and rods, while the octahedrons reveal an apparent activation energy of 65 kJ/mol. The reaction order in O2 is positive (0.26–0.32). Under mild reaction conditions, all three morphologies are stable, consistent with corresponding studies of CeO2 powders and CeO2 nanofibers. Under harsh reaction conditions, however, cubes and octahedrons are both instable, forming hydrated CeCl3, while rods are still stable. The present stability and activity experiments in the catalytic HCl oxidation reaction over shape-controlled CeO2 nanoparticles may serve as benchmarks for future ab initio studies of the catalyzed HCl oxidation reaction over well-defined CeO2 surfaces.
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