Search results for "Electrochemical reduction"
showing 10 items of 21 documents
Electrochemical conversion of CO2 to HCOOH at tin cathode in a pressurized undivided filter-press cell
2018
Abstract The electrochemical reduction of carbon dioxide to formic acid was performed for the first time in a pressurized filter-press cell with a continuous recirculation of the electrolytic solution (0.9 L) at a tin cathode. It was shown that the performances of the system are comparable or slightly better than that of a batch system with a smaller volume (0.05 L). The selection of proper values of both current density and CO2 pressure allowed to achieve quite high values of faradaic efficiencies. Long-time electrolyses have shown that the system is stable and that it can allow to generate quite high concentrations of HCOOH (about 0.4 M).
Development of an Electrochemical Process for the Simultaneous Treatment of Wastewater and the Conversion of Carbon Dioxide to Higher Value Products
2016
Many researchers have shown that selected anodic processes allow effective treatment of a very large amount of wastewater contaminated by pollutants resistant to biological processes. In the meantime, various authors have also shown that carbon dioxide can be converted into higher value products, such as formic acid or synthesis gas, by cathodic reduction at suitable cathodes. These two processes present interesting economic potential that, however, still needs to be improved for further development at an industrial level. Herein, these two kinds of process are combined in the same cell to improve their economic feasibility. In particular, the anodic treatment of wastewater at a boron-doped…
Front Cover: (Photo)electrocatalytic Versus Heterogeneous Photocatalytic Carbon Dioxide Reduction (ChemPhotoChem 9/2021)
2021
Homogeneous Metal-Based Catalysis in Supercritical Carbon Dioxide as Reaction Medium
2016
Above 31.1 degrees C and 73.8 bar, carbon dioxide reaches the supercritical state, being transformed into a fluid (scCO(2)) that has attracted interest in the last few decades as reaction medium for several transition-metal-catalyzed organic transformations. The main feature of this fluid rests on its capability to dissolve large amounts of other gases such as hydrogen, carbon monoxide, ethylene, or even methane and light alkanes. In this manner, very high concentrations of these reactants are available for catalysis. In this contribution a review of the main achievements of the use of transition-metal complexes as catalysts in scCO(2) is presented.
Baeyer–Villiger oxidation of ketones with a silica-supported peracid in supercritical carbon dioxide under flow conditions
2009
[2-Percarboxyethyl]-functionalized silica reacts with ketones in supercritical carbon dioxide at 250 bar and 40 °C under flow conditions to yield the corresponding esters and lactones. The solid reagent can be easily recycled through treatment with 70% hydrogen peroxide in the presence of an acid at 0 °C. This procedure not only simplifies the isolation of the reaction products, but has the advantage of using only water and carbon dioxide as solvents under mild conditions.
Electrochemical reduction of carbon dioxide to formic acid at a tin cathode in divided and undivided cells: effect of carbon dioxide pressure and oth…
2016
Abstract The reduction of carbon dioxide to formic acid at a tin cathode was studied in both divided and undivided cells. In the first stage of the study, the effect of some operating parameters, including the working potential and the nature of the supporting electrolyte and of the cathode, on both the cathodic reduction of CO2 and the anodic oxidation of formic acid was investigated in a divided cell. In a second stage, the reduction of carbon dioxide was performed in an undivided cell with the aim of studying the effect on the generation of formic acid of various operating parameters such as current density, cathode to anode area ratio, mixing rate and nature of the anode and of the supp…
In Situ Regeneration of Copper-Coated Gas Diffusion Electrodes for Electroreduction of CO2 to Ethylene
2021
This research was funded by the European Union’s Horizon 2020 research and innovation program under grant agreement No 768789 as well as by the Polish National Centre of Science under grant no 2017/26/D/ST8/00508. The Institute of Solid State Physics, University of Latvia, as a center of excellence, has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement no. 739508, project CAMART2.
(Photo)electrocatalytic Versus Heterogeneous Photocatalytic Carbon Dioxide Reduction
2021
The present review summarizes some of the main results achieved in electrochemical, photocatalytic, and (photo)-electrocatalytic systems for the reduction of carbon dioxide. After a preliminary survey of the electrocatalytic and photocatalytic systems in terms of materials used, efficiencies, operating conditions, and product distribution, it is shown how the combination of the two approaches affords often higher efficiency than the single technologies and allows better control of the product distribution. In fact, the peculiar energetic distribution at the interface of irradiated semiconductors under opportune electrical bias enables enhancement of the spatial separation of the photogenera…
On the electrochemical reduction of carbon dioxide and ethylene
1973
Die gemeinsame Elektrolyse von Athylen (I) und Kohlendioxid (II) liefert je nach den angewandten Bedingungen Mischungen aus Oxalsaure (III) und Bemsteinsaure (IV).