Related Experiment Video
Updated: Nov 27, 2025

Synthesis and Testing of Supported Pt-Cu Solid Solution Nanoparticle Catalysts for Propane Dehydrogenation
Published on: July 18, 2017
Bimetallic AgPd/UiO-66 Hybrid Catalysts for Propylene Glycol Oxidation into Lactic Acid
Sergey Ten1, Viktoriia V Torbina1, Vladimir I Zaikovskii2
1Laboratory of Catalytic Research, Tomsk State University, 36 Lenin Ave., 634050 Tomsk, Russia.
Abstract:
Different methods (the wetness impregnation of Ag and Pd precursors dissolved in water or acetonitrile solution, and the double solvent impregnation technique) were employed to immobilize Ag-Pd nanoparticles (NPs) into the pores of the microporous zirconium-based metal-organic framework known as UiO-66. The obtained materials were characterized by using nitrogen adsorption-desorption at -196 °C, powder X-ray diffraction, UV-Vis diffusion reflectance spectroscopy, and transition electron microscopy measurements. Special attention was paid to the acid and redox properties of the obtained materials, which were studied by using temperature-programmed desorption of ammonia (TPD-NH3) and temperature-programmed reduction (TPR-H2) methods. The use of a drying procedure prior to reduction was found to result in metallic NPs which, most likely, formed on the external surface and were larger than corresponding voids of the metal-organic framework. The formation of Ag-Pd alloy or monometallic Ag and Pd depended on the nature of both metal precursors and the impregnation solvent used. Catalytic activity of the AgPd/UiO-66 materials in propylene glycol oxidation was found to be a result of synergistic interaction between the components in AgPd alloyed NPs immobilized in the pore space and on the external surface of UiO-66. The key factor for consistent transformation of propylene glycol into lactic acid was the proximity between redox and acid-base species.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is activated by...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...

