Activation of Surface ReOx Sites on Al2O3 Catalysts for Olefin Metathesis

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• 作者：Soe Lwin ; Yuanyuan Li ; Anatoly I. Frenkel ; Israel E. Wachs
• 刊名：ACS Catalysis
• 出版年：2015
• 出版时间：November 6, 2015
• 年：2015
• 卷：5
• 期：11
• 页码：6807-6814
• 全文大小：533K
• ISSN：2155-5435

文摘

The nature of activated surface ReO_x sites and surface reaction intermediates for supported ReO_x/Al₂O₃ catalysts during propylene self-metathesis were systematically investigated for the first time using in situ spectroscopy (Raman, UV鈥搗is, XAS (XANES/EXAFS) and IR). In situ Raman spectroscopy reveals that olefins selectively interact with the surface dioxo ReO₄ sites anchored at acidic alumina hydroxyls. In situ UV鈥搗is indicates that surface Re⁵⁺ and some Re⁶⁺ sites form, and in situ XAS indicates a reduction in the number of Re鈺怬 bond character in the propylene self-metathesis reaction environment, especially as the temperature is increased. The appearance of oxygenated products during propylene activation supports the conclusion that catalyst activation involves removal of oxygen from the surface rhenia sites (pseudo-Wittig mechanism). Isotopic CD₃CD鈺怌D₂ 鈫?CH₃CH鈺怌H₂ switch experiments demonstrate the presence of surface Re鈺怌D₂ and Re鈺怌DCD₃ reaction intermediates, with the surface Re鈺怌D₂ species being the most abundant reaction intermediate. In situ IR spectroscopy indicates the presence of significant surface propylene 蟺 complexes on alumina and rhenia sites of the catalyst, which complicates analysis of surface reaction intermediates during propylene self-metathesis.