首页> 外文期刊>Journal of Catalysis >SELECTIVE ACTIVATION OF C-H AND C=C BONDS ON METAL CARBIDES - A COMPARISON OF REACTIONS OF N-BUTANE AND 1,3-BUTADIENE ON VANADIUM CARBIDE FILMS ON V(110)
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SELECTIVE ACTIVATION OF C-H AND C=C BONDS ON METAL CARBIDES - A COMPARISON OF REACTIONS OF N-BUTANE AND 1,3-BUTADIENE ON VANADIUM CARBIDE FILMS ON V(110)

机译:金属碳化物上C-H和C = C键的选择性活化-V(110)上碳化钒薄膜上正丁烷和1,3-丁二烯反应的比较

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摘要

We have investigated the adsorption and decomposition of n-butane and 1,3-butadiene on clean and carbide-modified vanadium (110) surfaces. By using high-resolution electron energy loss spectroscopy and thermal desorption spectrometry, we observe that the formation of carbide significantly modifies the reactivities of vanadium. The 1,3-butadiene molecules interact strongly with clean V(110) via the interaction between the d-band of vanadium and the pi orbitals of the adsorbates; the interaction is much weaker on the carbide-modified surfaces. On the other hand, n-butane interacts very weakly and reversibly with the clean surface; the reactivity is enhanced on carbide-modified surfaces. These experimental results are compared to the existing theories on the activation of C-H bonds of alkanes and C=C bonds of unsaturated hydrocarbons on transition metals. Such a comparison indicates that, although the reactivities of clean vanadium agree very well with the theoretical predictions for early transition metals, the properties of carbide-modified surfaces are more similar to those of Group VIIIB metals. (C) 1995 Academic Press, Inc. [References: 50]
机译:我们研究了正丁烷和1,3-丁二烯在清洁的碳化物改性钒(110)表面上的吸附和分解。通过使用高分辨率电子能量损失谱和热脱附谱,我们观察到碳化物的形成显着改变了钒的反应性。 1,3-丁二烯分子通过钒的d-带与被吸附物的pi轨道之间的相互作用而与干净的V(110)强烈地相互作用。在碳化物改性表面上的相互作用弱得多。另一方面,正丁烷与清洁表面的相互作用非常弱且可逆。在碳化物改性的表面上反应性得到增强。将这些实验结果与现有的关于烷烃的C-H键和过渡金属上的不饱和烃的C = C键活化的理论进行了比较。这样的比较表明,尽管清洁钒的反应性与早期过渡金属的理论预测非常吻合,但碳化物改性的表面的性质与VIIIB族金属更为相似。 (C)1995 Academic Press,Inc. [参考:50]

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