Oxidation of glycerol with H2O2 on Pb-promoted Pd/Γ-Al2O3 catalysts (original) (raw)
Related papers
Novel fine-disperse bimetallic Pt-Pd/Al 2 O 3 catalysts for glycerol oxidation with molecular oxygen
IOP Conference Series: Materials Science and Engineering, 2013
Using extractive-pyrolytic method several Pt-Pd bimetallic catalysts supported on plasma-processed alumina nanopowder were synthesized. Pt-Pd loading and glycerol oxidation process parameter influence on catalyst activity and selectivity was determined oxidizing glycerol in mild conditions. Novel bimetallic catalysts in neutral water solutions were practically inactive (glycerol conversion was only 3%) whereas in alkaline solutions they were active and selective to glyceric acid. Using 1.2%Pt-1.2%Pd/Al 2 O 3 catalyst glyceric acid was obtained with 65% selectivity (glycerol conversion was 96%). It was shown that novel finedisperse bimetallic Pt-Pd/Al 2 O 3 catalysts were more active compared to analogous monometallic Pt/Al 2 O 3 and Pd/Al 2 O 3 catalysts.
Catalysts
Ceria-supported Pd catalysts encompassing oxides of Cu, Co, and Fe were synthesized and characterized using XRD, TEM, SEM-EDX, TPR, BET, and Raman. After the incorporation of the metal oxides, the surface area and pore volume of the ceria support decreased. XRD showed the presence of the metal oxide phases as well as the support, CeO2. TPR showed that the bimetallic catalyst had improved reducibility compared to the monometallic Pd/CeO2. TEM images showed irregular-shaped particles with an average size distribution of 2–10 nm. SEM-EDX showed that the metal oxides were evenly distributed over the surface of the support. The electro-oxidation of glycerol in an alkaline environment was evaluated using cyclic voltammetry, and the products formed were identified and quantified using GC-MS. Glyceric acid was the dominant product over Pd-CuO/CeO2, while glyceraldehyde and dihydroxyacetone were dominant over Pd-Co3O4/CeO2 and Pd-Fe2O3/CeO2, respectively.
Glycerol to Glyceraldehyde Oxidation Reaction Over Pt-Based Catalysts Under Base-Free Conditions
Frontiers in Chemistry, 2019
Glycerol valorization through partial oxidation is a good way of obtaining many different molecules with high added value such as glyceric acid, tartronic acid, dihydroxyacetone, etc. Among the potential products, glyceraldehyde is an interesting chemical compound for its various applications in different domains such as organic chemistry, medical, and cosmetic industries. In the present paper, we studied the effect of different supports on the glycerol oxidation reaction in a batch reactor applying base-free conditions. The tested catalysts were Pt-based materials deposited on various supports (i.e., SiO 2 , TiO 2 , ZSM-5, γ-Al 2 O 3), which were synthesized using a deposition method followed by a chemical reduction. The catalysts were extensively characterized (BET, ICP, XRD, TEM, XPS), highlighting differences in terms of specific surface areas, textural properties, and Pt nanoparticles sizes. We evidenced a direct relation between glycerol conversion and glyceraldehyde selectivity (i.e., an increase in glycerol conversion leads to a decrease in glyceraldehyde selectivity). The Pt/γ-Al 2 O 3 catalysts exhibited the highest activity, but their selectivity to glyceraldehyde significantly decreased with time on stream. Pt/SiO 2 presented the highest selectivity to glyceraldehyde owing to a slower reaction rate, which allows envisioning technical opportunities to continuously extract the formed glyceraldehyde from the mixture.
Glycerol oxidation reaction using PdAu/C electrocatalysts
Ionics, 2016
Glycerol oxidation reactions were evaluated using PdAu/C electrocatalysts under alkaline conditions. These electrocatalysts were synthesized in different ratios (100:0, 75:25, 50:50, 25:75, and 0:100), using the borohydride reduction method. The materials were characterized with X-ray diffraction (XRD), transmission electron microscopy (TEM), and electrochemical techniques associated by in situ attenuated total reflectance Fourier transformed infrared spectroscopy (ATR-FTIR). According to the XRD diffractograms, the presence of Pd and Au (face-centered cubic (fcc)) phases and Pd-Au (fcc) alloys were detected. Cyclic voltammetry assisted by ATR-FTIR in situ and chronoamperometry experiments revealed that the addition of Au remarkably enhances the electrocatalytic activity, due to the action of bifunctional effect, with addition of the interactions of alcohoxide with hydroxylate species in gold surface, and the stability of Pd/C catalysts. Highest current density (≈4 mA mg metal −1) was achieved for the catalyst Pd 50 Au 50 /C and Pd 75 Au 25 /C, which is two times higher than that achieved by Pd/C (2 mA mg metal −1), demonstrating the beneficial effect of the PdAu alloy.
Catalysts
The catalytic conversion of glycerol to value-added propanols is a promising synthetic route that holds the potential to overcome the glycerol oversupply from the biodiesel industry. In this study, selective hydrogenolysis of 10 wt% aqueous bio-glycerol to 1-propanol and 2-propanol was performed in the vapor phase, fixed-bed reactor by using environmentally friendly bifunctional Pd/MoO3-Al2O3 catalysts prepared by wetness impregnation method. The physicochemical properties of these catalysts were derived from various techniques such as X-ray diffraction, NH3-temperature programmed desorption, scanning electron microscopy, 27Al NMR spectroscopy, surface area analysis, and thermogravimetric analysis. The catalytic activity results depicted that a high catalytic activity (>80%) with very high selectivity (>90%) to 1-propanol and 2-propanol was obtained over all the catalysts evaluated in a continuously fed, fixed-bed reactor. However, among all others, 2 wt% Pd/MoO3-Al2O3 catalys...
Oxidation of glycerol over AuPt catalysts
", Journal of the South African Institute of Mining and Metallurgy 112 (2012), 577-581
Gold has been demonstrated as a possible catalyst for oxidation reactions. Some evidence for a possible promotion effect of platinum has also been recorded. The influence of platinum as promoter for Au/γ-Al2O3 prepared via anionic ion-exchange for the oxidation of glycerol was investigated in a batch reactor at 60°C. It is inferred that the addition of platinum reduces the catalytic activity and the rate of deactivation, resulting in an overall higher final conversion of glycerol with increasing platinum loading. The addition of platinum to the catalyst favours the formation of the desired product, glyceric acid.