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Oxidation of Benzyl Alcohol Using Cobalt Oxide Supported Inside and Outside Hollow Carbon Spheres

机译:使用钴氧化物中空碳球的氧化钴氧化

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摘要

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.
机译:通过使用两种不同的聚合物模板合成负载中空碳球内外(HCSS)的氧化钴纳米颗粒(6nm)。苄醇的氧化用作模型反应以评估催化剂。 PXRD研究表明,由于碳的CO的还原,不同催化剂的共氧化状态变化,并且在苄醇氧化之前的金属氧化步骤增强了催化活性。金属负荷影响了催化效率,并且随着金属负荷的增加而降低,可能是由于孔隙填充效果。催化剂显示相似的活性和选择性(对苯甲醛)是否放置在HC(60%转化率下63%选择性63%的选择性)中。由于产品在HCS中累积而没有观察到中毒。

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