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Performance of bimetallic PdRu catalysts supported on gamma alumina for 2-ethylanthraquinone hydrogenation

机译:γ氧化铝上负载的双金属PdRu催化剂对2-乙基蒽醌加氢的性能

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A series of bimetallic PdRu catalysts supported on γ-Al2O3 were prepared by incipient wetness impregnation method and were assessed in the 2-ethylanthraquinone hydrogenation process. It is found that the addition of Ru to Pd can improve the catalyst's activity and maintain high selectivity at the same time for 2-ethylanthraquinone hydrogenation. Several analysis techniques including N2 adsorption–desorption, ICP-AES, XRD, TEM, H2-TPR, H2-TPD and XPS were adopted for characterizing the structural and electronic properties of the samples. It is revealed that PdRu bimetallic system shows stronger hydrogen desorption behavior in contrast to the monometallic catalysts. In addition, the higher fraction of Pd2+ and the presence of Ru4+ in the PdRu system may act as the electrophilic sites for the adsorption and activation of the CO of the 2-ethylanthraquinone molecule through the lone electron pair of the oxygen atom. These factors may be attributed to the superior performance of PdRu bimetallic samples for 2-ethylanthraquinone hydrogenation.
机译:采用初期湿润浸渍法制备了一系列负载在γ-Al 2 O 3 上的双金属PdRu催化剂,并在2-乙基蒽醌氢化过程中进行了评估。发现将Ru添加到Pd中可以提高催化剂的活性并同时维持2-乙基蒽醌氢化的高选择性。 N 2 吸附-解吸,ICP-AES,XRD,TEM,H 2 -TPR等几种分析技术,H 2 -TPD和XPS用来表征样品的结构和电子性能。揭示了与单金属催化剂相比,PdRu双金属体系表现出更强的氢解吸行为。此外,PdRu系统中较高比例的Pd 2 + 和Ru 4 + 的存在可能通过氧原子的孤电子对充当2-乙基蒽醌分子的CO的吸附和活化的亲电部位。这些因素可能归因于PdRu双金属样品对2-乙基蒽醌氢化的优异性能。

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