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首页> 外文期刊>chemistryselect >Selective Phenol Production by Hydrothermal Dehydrogenation of Cyclohexanone over Pd/C without External Oxygen and Hydrogen
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Selective Phenol Production by Hydrothermal Dehydrogenation of Cyclohexanone over Pd/C without External Oxygen and Hydrogen

机译:环己酮在Pd/C上水热脱氢选择性生产苯酚,无需外界氧氢

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摘要

An efficient and greener method for the hydrothermal dehydrogenation of cyclohexanone to phenol using recyclable Pd/C catalyst without external O-2 and H-2 was first reported. Pd/C as catalyst exhibited an excellent catalytic performance and hydrothermal stability for the present transformation, and phenol from cyclohexanone was produced in 60.4 yield with 100 selectivity. TON of 8.27 and TOF of 3.31 h(-1) were achieved, respectively. A poisoning experiment with Hg indicated that Pd/C catalyst was a heterogenous active species. Moreover, Pd/C can be recycled several times without loss of its activity. The scope of substrates, such as substituted ethyl, methyl, phenyl groups and diketones, were investigated under the optimized conditions, and the results showed that more bulky groups exerted a significant influence on the formation of phenol. A possible mechanism for the hydrothermal dehydrogenation of cyclohexanone to phenol was also proposed.
机译:首次报道了一种高效、更环保的环己酮水热脱氢制苯酚的方法,该方法采用可回收的Pd/C催化剂,无需外部O-2和H-2。Pd/C作为催化剂,在转化过程中表现出优异的催化性能和水热稳定性,以60.4%的收率和100%的选择性制备了环己酮苯酚。TON分别为8.27和TOF为3.31 h(-1)。汞中毒实验表明,Pd/C催化剂是一种异质活性物质。此外,Pd/C可以多次回收而不会损失其活性。在优化条件下研究了取代乙基、甲基、苯基和二酮等底物的范围,结果表明,更大的基团对苯酚的形成有显著影响。还提出了环己酮水热脱氢制苯酚的可能机理。

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