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Oxidation of cyclohexanol and cyclohexene with triazenido complexes of chromium immobilized in biosorption FAU supports

机译:固定在生物吸附FAU载体中的铬的三氮烯配合物氧化环己醇和环己烯

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摘要

This work presents the recovery of biosorption supports as an alternative source of benign production of heterogeneous catalysts for oxidation reactions in mild conditions. Cr-containing FAU zeolite, in sodium form (NaY) and in proton form (HY), was recovered from biosorption studies and reused as support for the preparation of heterogeneous catalysts by the flexible ligand method, using 1,3-diphenyltriazene derivatives. Results showed that the ligand play an important role in the coordination of Cr inside the zeolite. The catalysts showed good activity for the oxidation of cyclohexanol, reaching a maximum of 63.5% conversion. Cr leaching was evaluated and it was found that the Cr-FAU supports lost some of the Cr into the reaction medium, whereas immobilization of Cr-complexes reduced the referred leaching. For the cyclohexene oxidation, a maximum 72.9% conversion was achieved with a HY zeolite-based catalyst.
机译:这项工作提出了生物吸附载体的回收,作为温和条件下氧化反应良性生产非均相催化剂的替代来源。从生物吸附研究中回收了钠形式(NaY)和质子形式(HY)的含铬FAU沸石,并使用1,3-二苯基三氮烯衍生物通过挠性配体法将其用作制备多相催化剂的载体。结果表明,配体在沸石内部Cr的配位中起重要作用。该催化剂对环己醇的氧化表现出良好的活性,最大转化率为63.5%。评价了Cr的浸出,发现Cr-FAU载体将一些Cr损失到反应介质中,而Cr-络合物的固定化减少了所述的浸出。对于环己烯氧化,使用HY沸石基催化剂可获得最高72.9%的转化率。

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