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Thermodynamics of Methacrylate Synthesis from Methanol and a Propionate

机译:由甲醇和丙酸酯合成甲基丙烯酸酯的热力学

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摘要

Methacrylate monomers can be formed by the reaction of methanol and a propionate, e.g., propionic acid, propionic anhydride, or methyl propionate. Formaldehyde, a necessary reaction intermediate, can be produced from methanol via either dehydrogenation or partial oxidation. The equilibrium compositions for several variations of this chemistry were calculated as a function of temperature, total pressure, and inlet composition using a free-energy minimization technique. The thermodynamic analysis revealed that the methanol dehydrogenation route gave higher propionate conversion and selectivity than the partial oxidation alternative. For the dehydrogenation route, both conversion and selectivity were favored by high temperature and high methanol/propionate feed ratio. The calculations also showed that a methyl propionate feed produces the least amount of water and diethyl ketone, two byproducts which can complicate any process design for this chemistry.
机译:甲基丙烯酸酯单体可以通过甲醇与丙酸酯例如丙酸,丙酸酐或丙酸甲酯的反应形成。甲醛是必要的反应中间体,可以通过脱氢或部分氧化从甲醇中制得。使用自由能最小化技术,根据温度,总压力和进口成分计算出该化学物质几种变化形式的平衡成分。热力学分析表明,与部分氧化替代方法相比,甲醇脱氢途径具有更高的丙酸酯转化率和选择性。对于脱氢路线,高温和高甲醇/丙酸酯进料比有利于转化率和选择性。计算还表明,丙酸甲酯进料产生的水和二乙基酮的量最少,这两种副产物会使该化学反应的任何工艺设计复杂化。

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