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Direct liquid phase hydroxylation of benzene with an inner-circulated H2-O2 mixture over Pd or Pd-V modified Hβ catalysts at ambient conditions

机译:在环境条件下通过Pd或Pd-V改性Hβ催化剂直接苯的苯与内循环的H2-O2混合物的液相羟基化

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The direct liquid phase hydroxylation of benzene with hydrogen (H2)-oxygen (O2) mixture was achieved through a sealed gaseous inner-circulated process in the presence of Pd-V modified H catalyst. The results indicated that Pd-V modified H with an atomic ratio of V to Pd for 4 possessed the best catalytic performance and that acidic acid aqueous solution was the excellent media for direct hydroxylation of benzene with H2 and O2. Under the optimum reaction conditions, a relatively high formation rate of phenol (41.5 mmol PhOH/mmol Pd.h) and highly-efficient utilization of H2-O2 mixture as well as negligible loss of benzene volatilization could be simultaneously realized at 333 K. Besides, a synergistic mechanism was proposed to explain the favorable effects of introducing V oxides and adding water in acetic acid medium.
机译:通过在PD-V改性的H催化剂存在下通过密封的气态内循环过程实现苯的直接液相羟基(H 2) - 氧基(O 2)混合物。结果表明,具有V至Pd的原子比的PD-V改性H具有最佳的催化性能,并且酸性水溶液是具有H 2和O 2的直接羟基化的优异培养基。在最佳反应条件下,在333k的情况下,可以同时实现相对高的苯酚(41.5mmol / mmol pd.h)和高效利用H2-O2混合物的使用以及可忽略的苯挥发的损失。此外,可以同时实现提出了一种协同机制,以解释在乙酸培养基中引入v氧化物和加水的良好影响。

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