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Ceria supported gold-platinum catalysts for the selective oxidation of alkyl ethoxylates

机译:陶瓷支持金铂催化剂,用于选择性氧化烷基乙氧基化的催化剂

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This work covers the development of a ceria based AuPt catalyst for the selective aerobic oxidation of alkyl ethoxylates to their corresponding carboxylic acids. By optimizing metal loading and the Au to Pt ratio the activity of the catalyst could be increased significantly, while maintaining total selectivity. Although the choice of ceria as a support helped to suppress intermediate metal leaching, the catalyst still showed poor long-term stability in repeated batches. The cause for deactivation could finally be identified by TPR studies as over-oxidation. These suspicions were confirmed by a long-term stability study in continuous-mode. It proved to be possible to deactivate the catalyst on purpose by employing unfavourable oxidising reaction conditions, i.e. low substrate concentrations and excess oxygen. By avoiding such unfavourable conditions either in continuous-flow mode or in repeated batches, the long-term stability of the catalyst increased tremendously. A substrate screening of various ethoxylates showed that the catalyst was very well-suited to selectively oxidize a wide range of alkyl ethoxylates.
机译:这项工作涵盖了基于二氧化碳的催化剂的开发,用于将烷基乙氧基化的有氧氧化与其相应的羧酸的选择性有氧氧化。通过优化金属载荷和AU与PT的比率,可以显着增加催化剂的活性,同时保持总选择性。尽管选择二氧化碳作为支持有助于抑制中间金属浸出,但催化剂在重复批处理中仍然表现出较差的长期稳定性。 TPR研究最终可以将失活的原因确定为过度氧化。这些怀疑通过连续模式的长期稳定研究证实。事实证明,通过使用不利的氧化反应条件,即低底物浓度和过量的氧气,可以故意停用催化剂。通过避免在连续流模式下或重复批处理中避免这种不利条件,催化剂的长期稳定性大大增加。对各种乙氧基化物的底物筛选表明,催化剂非常适合选择性地氧化各种烷基乙氧基化的乙氧基化。

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