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Selective phenol hydrogenation under mild condition over Pd catalysts supported on Al2O3 and SiO2

机译:在Al 2 O 3和SiO2上负载的Pd催化剂的温和条件下的选择性酚氢化

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摘要

Cyclohexanone (CHONE) is the key intermediate in the manufacture of nylon-6 and nylon-66. Selective hydrogenation of phenol into CHONE was investigated over Pd/SiO2 and Pd/Al2O3. The results show that the yield of CHONE reaches 98% or more over Pd/Al2O3 and Pd/SiO2 at 333K under atmospheric pressure in cyclohexane solvent. High activity of Pd/Al2O3 is promoted by Lewis acidity, and phenol can be converted 100% within 300min. The hydrogenation of CHONE occurs until the conversion of phenol approaches completion. Pd/SiO2 with smaller Pd nano-particles presents higher selectivity. For polar solvent, such as ethanol and dichloromethane, the activity of Pd catalysts decreases greatly. Auxiliary experiments verify that phenol adsorbs on Pd catalysts via the formation of -c with an aromatic ring. Increased hydrogen pressure not only promotes significantly the rates of hydrogenation, but also increases the selectivity for CHONE, especially over Pd/SiO2-1 catalyst.
机译:环己酮(CHONE)是尼龙-6和尼龙-66制造的关键中间体。 研究了Pd / SiO 2和Pd / Al 2 O 3上研究了苯酚中苯酚的选择性氢化。 结果表明,在环己烷溶剂的大气压下,CoNe的产率在333K下在333K上达到98%或更多。 通过路易斯酸度促进Pd / Al2O3的高活性,并且苯酚可以在300ml内转化为100%。 浓缩ChOne的氢化直到苯酚接近完成的转化。 具有较小PD纳米颗粒的Pd / SiO2具有更高的选择性。 对于极性溶剂,例如乙醇和二氯甲烷,Pd催化剂的活性大大降低。 辅助实验通过用芳环的形成,通过形成-C,辅助实验证明苯酚对Pd催化剂进行脂肪。 增加的氢气压力不仅促进了氢化的速率,而且还增加了Chone的选择性,特别是在Pd / SiO 2 1催化剂上。

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