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Aerobic oxidation of cyclohexane by gold-based catalysts: New mechanistic insight by thorough product analysis

机译:金基催化剂有氧氧化环己烷:通过全面的产品分析获得新的机械原理

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摘要

The selective oxidation of cyclohexane to cyclohexanone and cyclohexanol with air over Au/Al_2O_3, Au/TiO_2, and Au/SBA-15 catalysts was investigated and compared with the industrial autoxidation process. In contradiction with the literature results, the Au-based catalysts did not exhibit excellent catalytic performance and the combined selectivity toward cyclohexanone and cyclohexanol decreased to ~70% with the increasing conversion above 5%. In addition, the observed product evolution and by-product evolution were typical for the autoxidation process, although a significant increase in adipic acid and CO_2 formation was observed. Additional oxidation experiments containing a radical scavenger completely inhibited the reaction and provided proof that the oxidation follows a radical-chain mechanism instead of a catalytic mechanism. This explains the low selectivity at increasing conversion. This important deviation from the literature results can be clarified by the complicated but necessary product analysis of both the gas and the liquid phases.
机译:研究了空气在Au / Al_2O_3,Au / TiO_2和Au / SBA-15催化剂上用空气将环己烷选择性氧化为环己酮和环己醇的方法,并将其与工业自氧化工艺进行了比较。与文献结果相反,金基催化剂没有表现出优异的催化性能,并且随着转化率的增加超过5%,对环己酮和环己醇的组合选择性降低至〜70%。另外,尽管观察到己二酸和CO_2形成显着增加,但是观察到的产物演变和副产物演变对于自氧化过程是典型的。包含自由基清除剂的其他氧化实验完全抑制了反应,并提供了证明氧化遵循自由基链机理而非催化机理的证据。这解释了增加转化率时的低选择性。与文献结果的重要偏离可以通过对气相和液相的复杂但必要的产物分析来阐明。

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