4.7 Article

Aerobic oxidative esterification of primary alcohols over Pd-Au bimetallic catalysts supported on mesoporous silica nanoparticles

Journal

CATALYSIS TODAY
Volume 306, Issue -, Pages 81-88

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cattod.2017.01.046

Keywords

Mesoporous silica nanoparticles; Bimetallic catalysis; Oxidative esterification; Tandem catalysisa

Funding

  1. U.S. Department of Energy under Center for Catalytic Hydrocarbon Functionalization, an Energy Frontier Research Center [DE-SC0001298]

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We have prepared a series of mesoporous silica nanoparticle (MSN) supported Pd-Au bimetallic catalysts using a newly developed sequential impregnation method. These catalysts were fully characterized by various techniques including nitrogen sorption, powder X-ray diffraction, inductively coupled plasma mass spectrometry (ICP-MS), transmission electron microscopy (TEM) and high angle annular dark-field scanning transmission electron microscopy (HADDF-STEM). By using this synthetic approach, we observed metal nanoparticles (NP) with diameters of 1-2 nm homogeneously supported on the MSN. Thecatalytic performance of these MSN supported metal NPs was tested by aerobic oxidative esterificationin a tandem reaction where primary alcohols are oxidized to their corresponding aldehydes and to esters in a subsequent reaction. We determined that Pd NPs are very efficient in the first step of oxidation; however, stagnant in the subsequent oxidation. On the contrary, Au NPs show slow reactivity in converting alcohols to aldehydes, but extraordinarily efficient in the oxidation of aldehydes to esters. By fine tuning the metal ratio, the bimetallic catalyst exhibits better reactivity and selectivity toward a variety of primary alcohols than the corresponding monometallic catalysts. In addition, we also found that the bimetallic Pd-Au@MSN catalysts can be recycled three times without a significant loss in activity. (c) 2017 Elsevier B.V. All rights reserved.

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