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Heterogeneous Transesterification of Dimethyl Carbonate and Phenol to Diphenyl Carbonate over Vanadium Pentoxide Microstructures

机译:五氧化二钒微观结构上碳酸二甲酯和苯酚的异质酯交换反应生成碳酸二苯酯

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摘要

Vanadium pentoxide (V2O5) microstructures were synthesized by calcining acidtreated NH4VO3 at 773 K in air, which were used as heterogeneous catalysts for the synthesis of diphenyl carbonate (DPC) by the transesterification of dimethyl carbonate (DMC) with phenol. The effects of the types of acid and the transesterification reaction time on catalytic activities were investigated. Under the conditions of reaction temperature of 453 K, a catalyst amount of 0.2% (molar ratio to phenol), molar ratio of DMC/phenol of 1:2 and a reaction time of 13 h, the maximum conversion of DMC and total yields of methyl phenyl carbonate (MPC) and DPC were 23.23 and 23.44%, respectively. The selectivity to the transesterification was nearly 100%. The plausible mechanism of the transesterification catalyzed by the V2O5 microstructures was also probed preliminarily. X-ray diffraction (XRD) and field-emission scanning electron microscopy (FE-SEM) characteristics of the catalyst samples had been recorded.
机译:通过在空气中773 K下煅烧酸处理的NH4VO3来合成五氧化二钒(V2O5)的微结构,这些结构可用作多相催化剂,通过碳酸二甲酯(DMC)与苯酚的酯交换反应合成碳酸二苯酯(DPC)。研究了酸的种类和酯交换反应时间对催化活性的影响。在453 K的反应温度下,催化剂用量为0.2%(与酚的摩尔比),DMC /苯酚的摩尔比为1:2,反应时间为13 h,DMC的最大转化率和总收率为碳酸甲基苯基酯(MPC)和DPC分别为23.23%和23.44%。酯交换反应的选择性接近100%。初步探讨了由V2O5微观结构催化的酯交换反应的合理机制。记录了催化剂样品的X射线衍射(XRD)和场发射扫描电子显微镜(FE-SEM)特性。

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