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负载型CrO3/ZrO2催化剂上丙烷氧化脱氢的原位紫外-可见-近红外漫反射和拉曼光谱及催化活性研究

In situ UV-vis-NIR diffuse reflectance and Raman spectroscopy and catalytic activity studies of propane oxidative dehydrogenation over supported CrO3/ZrO2 catalysts.

作者信息

Malleswara Rao T V, Deo Goutam, Jehng Jih-Mirn, Wachs Israel E

机构信息

Department of Chemical Engineering, Indian Institute of Technology, Kanpur 208 016, India.

出版信息

Langmuir. 2004 Aug 17;20(17):7159-65. doi: 10.1021/la049590v.

Abstract

The molecular structures, oxidation states, and reactivity of 3 and 6% CrO3/ZrO2 catalysts prepared by incipient wetness impregnation were examined under different conditions. The in situ Raman spectroscopic studies under dehydrated conditions reveal that the 3 and 6% CrO3/ZrO2 catalysts possess equal amounts of monochromate and polychromate species. Consequently, monolayer coverage on this ZrO2 support is about 3% CrO3. The 6% CrO3/ZrO2 possesses an additional Raman band due to Cr2O3 crystals corresponding to the remaining 3% CrO3. Furthermore, during reaction conditions the polychromate species is preferentially reduced, the monochromate species are slightly affected, and the Cr2O3 crystals are not affected. The in situ UV-vis-NIR diffuse reflectance spectroscopy results reveal that under steady-state reaction conditions the extent of reduction and edge energy position of surface Cr6+ cations increase with an increase in reduction environment for the 3 and 6% CrO3/ZrO2 samples. Propane oxidative dehydrogenation (ODH) studies reveal that the catalytic activity expressed in moles of propane converted per gram catalyst per second is similar for the two catalysts, which is consistent with equal amounts of molecularly dispersed chromia present. The turnover frequency for the 6% CrO3/ZrO2 catalyst is, however, smaller than that for the 3% CrO3/ZrO2 sample due to the presence of Cr2O3 crystals, which are relatively inactive for propane ODH. For this catalytic system and for the experimental conditions used, propene, CO, and CO2 are primary products. Furthermore, the 33-39% propene selectivity is not affected by the C3H8/O2 ratio for both catalysts. Structure-reactivity studies suggest that the molecularly dispersed species are present in equal amounts in the 3 and 6% CrO3/ZrO2 samples as Cr6+ monochromate and polychromate species are the most effective catalytic active sites taking part in the propane ODH reaction.

摘要

通过初湿浸渍法制备的3%和6% CrO₃/ZrO₂催化剂的分子结构、氧化态和反应活性在不同条件下进行了研究。脱水条件下的原位拉曼光谱研究表明,3%和6% CrO₃/ZrO₂催化剂具有等量的单铬酸盐和多铬酸盐物种。因此,在该ZrO₂载体上的单层覆盖率约为3% CrO₃。6% CrO₃/ZrO₂由于Cr₂O₃晶体而具有额外的拉曼带,对应于剩余的3% CrO₃。此外,在反应条件下,多铬酸盐物种优先被还原,单铬酸盐物种受到轻微影响,而Cr₂O₃晶体不受影响。原位紫外-可见-近红外漫反射光谱结果表明,在稳态反应条件下,对于3%和6% CrO₃/ZrO₂样品,随着还原环境的增加,表面Cr⁶⁺阳离子的还原程度和边缘能量位置增加。丙烷氧化脱氢(ODH)研究表明,以每克催化剂每秒转化的丙烷摩尔数表示的催化活性对于两种催化剂是相似的,这与存在等量的分子分散氧化铬一致。然而,由于存在对丙烷ODH相对不活泼的Cr₂O₃晶体,6% CrO₃/ZrO₂催化剂的周转频率小于3% CrO₃/ZrO₂样品。对于该催化体系和所使用的实验条件,丙烯、CO和CO₂是主要产物。此外,两种催化剂的33 - 39%的丙烯选择性不受C₃H₈/O₂比的影响。结构-反应活性研究表明,在3%和6% CrO₃/ZrO₂样品中,分子分散物种以等量存在,因为Cr⁶⁺单铬酸盐和多铬酸盐物种是参与丙烷ODH反应的最有效催化活性位点。

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