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Gold nanoparticles supported on Ce-Zr oxides for the oxidative esterification of aldehydes to esters

机译:在CE-ZR氧化物上支撑的金纳米颗粒,用于将醛的氧化酯化为酯

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Au nanoparticles supported on Ce-Zr oxides were prepared and characterized in order to study the role of the support in the oxidative esterification of aldehydes in the presence of molecular oxygen. Ce-Zr solid solutions were synthesized by using (NH4)(2)Ce(NO3)(6) as a precursor, while the mixed oxides were obtained by using a Ce(NO3)(3) precursor. The solid solutions exhibited a smaller crystallite size, higher BET surface area, larger amount of H-2 consumption, and higher acidity and basicity than the mixed oxides at the same Ce/Zr molar ratio due to the incorporation of Zr4+ into the ceria lattice. The effect of the support was investigated because all the samples presented similar Au particle sizes, as confirmed by the HAADF-STEM study. Supports with higher reducibility showed better performance by activating methanol to methoxy and facilitating the beta-H elimination of hemiacetal. We also found that the formation of hemiacetal was enhanced by the acidic sites and basic sites of Au catalysts supported on solid solutions possessing similar reducibility. A plausible reaction mechanism for the oxidative esterification of aldehydes on Ce-Zr solid solution-supported Au nanoparticles was proposed. The screened catalyst was also applicable to the oxidative esterification of different benzylic aldehydes, producing high yields. This catalyst could be reused after a simple separation eight times, keeping a high selectivity of above 99%.
机译:制备了在CE-ZR氧化物上支撑的Au纳米颗粒并表征以研究在分子氧存在下支持在醛中的氧化酯化中的作用。通过使用(NH4)CE(NO3)(6)作为前体合成CE-ZR固体溶液,而使用CE(NO3)(3)前体获得了混合氧化物。与混合氧化物相比,由于将Zr4+掺入陶瓷晶格中,固体溶液表现出较小的结晶石尺寸,更高的BET表面积,较大的H-2消耗量以及更高的酸度和碱性。根据HAADF-STEM研究证实,研究了支持的效果,因为所有样品都呈现出相似的AU粒径。可降低性较高的支持通过将甲醇激活至甲氧基并促进β-H消除hemaiaIcetal显示出更好的性能。我们还发现,在具有相似可降低性的固体溶液上支撑的AU催化剂的酸性位点和基本位点增强了半斑的形成。提出了一种合理的反应机制,用于在CE-ZR固体溶液支持的Au纳米颗粒上氧化酯化的氧化酯化。筛选的催化剂也适用于不同苯并醛的氧化酯化,产生高产量。该催化剂可以在简单的分离八次后重复使用,使高于99%的高选择性。

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