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Infrared study of methyl formate and formaldehyde adsorption on reduced and oxidised silica-supported copper catalysts

机译:还原和氧化的二氧化硅负载的铜催化剂上甲酸甲酯和甲醛吸附的红外研究

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摘要

Infrared spectra are reported of methyl formate and formaldehyde adsorbed at 300 K on silica, Cu/SiO2 reduced in hydrogen and Cu/SiO2 which had been oxidised by exposure to nitrous oxide after reduction. Silanol groups on silica form hydrogen bonds with carbonyl groups in weakly adsorbed methyl formate molecules. Methyl formate ligates via its carbonyl groups to Cu atoms in the surface of reduced copper. A low residual concentration of surface oxygen on copper promoted the slow reaction of ligated methyl formate to give a bridging formate species on copper and adsorbed methoxy groups. Methyl formate did not ligate to an oxidised copper surface but was rapidly chemisorbed to give unidentate formate and methoxy species. Formaldehyde slowly polymerises on silica to form trioxane and other oxymethylene species. The reaction is faster over Cu/SiO2 which, in the reduced state, also catalyses the formation of bridging formate anions adsorbed on copper. The reaction between formaldehyde and oxidised Cu/SiO2 leads to both unidentate and bidentate formate and adsorbed water.
机译:红外光谱报道了在300 K吸附在二氧化硅上的甲酸甲酯和甲醛,氢中还原的Cu / SiO2和在还原后暴露于一氧化二氮而被氧化的Cu / SiO2的红外光谱。二氧化硅上的硅烷醇基团与弱吸附的甲酸甲酯分子中的羰基形成氢键。甲酸甲酯通过其羰基与还原的铜表面的Cu原子连接。铜上表面氧的低残留浓度促进了连接的甲酸甲酯的缓慢反应,从而在铜和吸附的甲氧基上形成桥连的甲酸类。甲酸甲酯未结扎至氧化的铜表面,但迅速被化学吸附,产生了未知的甲酸和甲氧基。甲醛在二氧化硅上缓慢聚合,形成三恶烷和其他甲醛。该反应比Cu / SiO 2更快,后者在还原状态下也催化吸附在铜上的桥连甲酸根阴离子的形成。甲醛和氧化的Cu / SiO2之间的反应会导致身份不明和二齿甲酸盐和吸附水。

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