首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Highly Efficient and Stable Vanadia-Titania-Sulfate Catalysts for Methanol Oxidation to Methyl Formate: Synthesis and Mechanistic Study
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Highly Efficient and Stable Vanadia-Titania-Sulfate Catalysts for Methanol Oxidation to Methyl Formate: Synthesis and Mechanistic Study

机译:高效稳定的钒钛-二氧化钛-硫酸盐催化剂催化甲醇氧化为甲基甲酸酯:合成及机理研究

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摘要

Vanadia-titania-sulfate nanocatalysts for methanol oxidation to methyl formate (ME) were prepared by coprecipitation. When calcinated at 400 degrees C, both methanol conversion and MF selectivity reached similar to 98.5% at reaction temperatures of 140-145 degrees C. Characterizations with several experimental techniques revealed the catalysts as highly dispersed vanadia supported by anatase titania with acidic sites of significant strength and density. The catalysts also showed very high stability with lifetime exceeding 4500 h. Extensive density functional theory calculations using both cluster and surface models revealed MF to form via the hemiacetal mechanism, involving the condensation of methanol and formaldehyde at acidic sites and methanol and hemiacetal oxidations at redox sites. The alternative formyl mechanism was predicted kinetically much less favorable, showing these catalysts to work in a distinct mechanism from the rutile titania photocatalyst. Interestingly, methanol chemisorption at redox sites leads to the formation of acidic sites capable of catalyzing the condensation reaction.
机译:通过共沉淀法制备了钒氧化钛-硫酸钛纳米催化剂,用于甲醇氧化为甲酸甲酯(ME)。在400摄氏度下煅烧时,在140-145摄氏度的反应温度下,甲醇转化率和MF选择性均达到98.5%左右。几种实验技术的表征表明,该催化剂为高度分散的钒,由锐钛矿型二氧化钛支撑,具有明显强度的酸性位点和密度。催化剂还显示出非常高的稳定性,使用寿命超过4500小时。使用簇模型和表面模型进行的广泛密度泛函理论计算表明,MF是通过半缩醛机理形成的,涉及酸性位点上甲醇和甲醛的缩合以及氧化还原位点上甲醇和半缩醛的氧化。预测动力学上不利的甲酰机理,表明这些催化剂以不同于金红石型二氧化钛光催化剂的机理起作用。有趣的是,甲醇在氧化还原位点的化学吸附导致形成能够催化缩合反应的酸性位点。

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