DSI-NRF Centre of Excellence in Strong Materials, University of the Witwatersrand, 2050, Johannesburg, South Africa.
Molecular Sciences institute, School of Chemistry, University of the Witwatersrand, 2050, Johannesburg, South Africa.
ChemistryOpen. 2021 Jun;10(6):618-626. doi: 10.1002/open.202000312. Epub 2021 May 2.
Cobalt oxide nanoparticles (6 nm) supported both inside and outside of hollow carbon spheres (HCSs) were synthesized by using two different polymer templates. The oxidation of benzyl alcohol was used as a model reaction to evaluate the catalysts. PXRD studies indicated that the Co oxidation state varied for the different catalysts due to reduction of the Co by the carbon, and a metal oxidation step prior to the benzyl alcohol oxidation enhanced the catalytic activity. The metal loading influenced the catalytic efficiency, and the activity decreased with increasing metal loading, possibly due to pore filling effects. The catalysts showed similar activity and selectivity (to benzaldehyde) whether placed inside or outside the HCS (63 % selectivity at 50 % conversion). No poisoning was observed due to product build up in the HCS.
钴氧化物纳米粒子(6nm)同时负载在空心碳球(HCS)的内外表面,通过使用两种不同的聚合物模板合成。以苯甲醇氧化为模型反应来评估催化剂。PXRD 研究表明,由于碳对 Co 的还原作用,不同催化剂的 Co 氧化态不同,并且在苯甲醇氧化之前的金属氧化步骤可以提高催化活性。金属负载量影响催化效率,并且随着金属负载量的增加,活性降低,这可能是由于孔填充效应。催化剂无论置于 HCS 内部还是外部,其活性和选择性(对苯甲醛)都相似(在 50%转化率下选择性为 63%)。由于产物在 HCS 中的积累,没有观察到中毒现象。