4.7 Article

Hydrogenation of quinolines, alkenes, and biodiesel by palladium nanoparticles supported on magnesium oxide

Journal

DALTON TRANSACTIONS
Volume 41, Issue 48, Pages 14490-14497

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt31533e

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Funding

  1. Donors of the American Chemical Society Petroleum Research Fund [47472-AC3]
  2. US Department of Energy [DEEE0003129]

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A new catalyst composed of Pd nanoparticles supported on MgO has been prepared by the room temperature NaBH4 reduction of Na2PdCl4 in methanol in the presence of the support. TEM measurements reveal well-dispersed Pd particles of mean diameter 1.7 nm attached to the MgO surface. Further characterization was achieved by ICP-AES, XPS, XRD, H-2 pulse chemisorption and H-2-TPR. The new catalyst is efficient for the regioselective hydrogenation of the heterocyclic ring of quinolines, as well as for the mild reduction of a variety of alkenes representative of fuel components, and the partial saturation of biodiesel. The new material is considerably more reactive than commercial Pd/SiO2 and Pd/Al2O3 catalysts under analogous reaction conditions.

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