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Liquid phase oxidation of toluene to benzaldehyde with molecular oxygen over copper-based heterogeneous catalysts

机译:Liquid phase oxidation of toluene to benzaldehyde with molecular oxygen over copper-based heterogeneous catalysts

摘要

We conducted the liquid phase oxidation of toluene with molecular oxygen over heterogeneous catalysts of copper-based binary metal oxides. Among the copper-based binary metal oxides, iron-copper binary oxide (Fe/Cu = 0.3 atomic ratio) was found to be the best catalyst. In the presence of pyridine, overoxidation of benzaldehyde to benzoic acid was partially prevented. As a result, highly selective formation of benzaldehyde (86% selectivity) was observed after 2 h of reaction (7% conversion of toluene) at 463 K and 1.0 MPa of oxygen atmosphere in the presence of pyridine. These catalytic performances were similar or better than those in the gas phase oxidation of toluene at reaction temperatures higher than 473 K and under 0.5-2.5 MPa. It was suggested from competitive adsorption measurements that pyridine could reduce the adsorption of benzaldehyde. At a long reaction time of 4 It, the conversion increased to 25% and benzoic acid became the predominant reaction product (72% selectivity) in the absence of pyridine. The yield of benzoic acid was higher than that in the Snia-Viscosa process, which requires corrosive halogen ions and acidic solvents in the homogeneous reaction media. The catalyst was easily recycled by simple filtration and reusable after washing and drying.
机译:我们在铜基二元金属氧化物的多相催化剂上用分子氧进行了甲苯的液相氧化。在铜基二元金属氧化物中,铁铜二元氧化物(Fe / Cu = 0.3原子比)被认为是最好的催化剂。在吡啶的存在下,部分防止了苯甲醛过氧化为苯甲酸。结果,在吡啶存在下,在463 K和1.0 MPa的氧气气氛下反应2小时(甲苯转化率为7%)后,观察到苯甲醛的高选择性形成(选择性为86%)。在高于473 K和0.5-2.5 MPa的反应温度下,这些催化性能与甲苯的气相氧化相似或更好。从竞争性吸附测量结果表明,吡啶可以减少苯甲醛的吸附。在4 It的较长反应时间下,转化率提高至25%,在不存在吡啶的情况下,苯甲酸成为主要的反应产物(选择性为72%)。苯甲酸的收率高于Snia-Viscosa工艺,后者在均相反应介质中需要腐蚀性的卤素离子和酸性溶剂。该催化剂易于通过简单的过滤而再循环,并且在洗涤和干燥后可重复使用。

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