Search results for "supporting electrolyte"
showing 9 items of 49 documents
Electrochemical technology for the treatment of real washing machine effluent at pre-pilot plant scale by using active and non-active anodes
2018
Abstract Real effluent of washing machine is one of the major sources of microplastics and fabrics in municipal and surface water. The effluents constitute large volume of wastewater with different surfactants since every household and industries nowadays use washing machine rather than traditional hand washing. In this work, a real effluent of washing machine was treated by electrooxidation (EO) in a pre-pilot plant scale electrochemical flow reactor using active (Ti/Pt) or non-active (boron doped diamond (BDD)) anodes and Ti cathode. The effect of anode material (Ti/Pt or BDD) and the applied current density (16.6, 33.3 and 66.6 mA cm−2) on the decay of the organic matter, in terms of che…
Electrochemical synthesis of sulfamides.
2021
Herein we demonstrate the first electrochemical synthesis protocol of symmetrical sulfamides directly from anilines and SO2 mediated by iodide. Sulfamides are an emerging functional group in drug design. Highlights are the direct use of SO2 from a stock solution and no necessity of any supporting electrolyte. Overall, the reaction has been demonstrated for 15 examples with yields up to 93%.
Metal‐Free Electrochemical Synthesis of Sulfonamides Directly from (Hetero)arenes, SO2, and Amines
2021
Abstract Sulfonamides are among the most important chemical motifs in pharmaceuticals and agrochemicals. However, there is no methodology to directly introduce the sulfonamide group to a non‐prefunctionalized aromatic compound. Herein, we present the first dehydrogenative electrochemical sulfonamide synthesis protocol by exploiting the inherent reactivity of (hetero)arenes in a highly convergent reaction with SO2 and amines via amidosulfinate intermediate. The amidosulfinate serves a dual role as reactant and supporting electrolyte. Direct anodic oxidation of the aromatic compound triggers the reaction, followed by nucleophilic attack of the amidosulfinate. Boron‐doped diamond (BDD) electro…
The correlation between electrochemical impedance spectra and voltammograms of PB films in aqueous NH4Cl and CsCl
1998
Abstract Voltammetric curves of reduction of Prussian Blue Films to the Everitt’s Salt form and oxidation to the Prussian Yellow form show important differences depending on the supporting electrolyte countercation. The rate of the overall electron-hopping depends on the countercation. Apparent diffusion coefficients are evaluated from impedance spectra at different stabilization potentials. The dependence of the apparent diffusion coefficients on the stabilization potential can help understand the dependence of the voltammograms shape on the countercation nature.
Electrochemical Oxidation of Carboxylic Acids in Water at Boron-Doped Diamond (BDD) Anodes in the Range of Potential of Oxygen Evolution: Detection M…
2013
The electrochemical oxidation in water solutions of selected carboxylic acids (namely oxalic, formic, acetic, maleic, and succinic) at boron-doped diamond (BDD) anodes was investigated by polarization and chronoamperometric measurements. In the presence of low concentrations of carboxylic acids, current densities changed approximately linearly with the acid concentrations. Furthermore, when the current densities were plotted as a function of the chemical oxygen demand, a similar response was observed for all the investigated acids with the exception of oxalic acid. For high carboxylic acid concentrations, the linear variation is often loosen and different behaviors are observed depending on…
Electrochemical behaviour of inorganic redox substances dispersed into Nafion® films
1999
Abstract The voltammetric response of a Nafion ® film deposited on an indium tin oxide (ITO) electrode was studied. It was observed that the response is affected by the thickness of the Nafion ® layer. Also, the voltammograms show differences depending on the concentration and composition of the supporting electrolyte solution. The ITO–Nafion ® system can be stabilised by repetitive cyclic voltammetry, and then the inner hydrogen reduction is not detected by electrochemical impedance spectroscopy. Different substances were dispersed into the Nafion ® matrix in order to study their electrochemical response.
Studien zum Vorgang der Wasserstoffübertragung, 41. Elektroreduktion von Acetophenon unter Mitwirkung optisch aktiver Leitsalze
1977
Die Anderung des Carbinol/Pinakol-Verhaltnisses2) (C/P) und der optischen Induktion bei der Elektroreduktion von Acetophenon mit (1 R, 2S)-N-(3-Cyanpropyl)-N-methylephedriniumbromid (1) und (1 R, 2 S)-N,N-Dimethylephedriniumbromid (2) als Leitsalze wird untersucht in Abhangigkeit: a) vom Potential (Tabelle 1), b) von der Stromdichte (Tabelle 2), c) von Pulsbedingungen (Tabelle 3), d) vom pH (Tabelle 4), e) von der Anwesenheit anderer Kationen (Tabelle 5), f) vom Losungsmittel (Tabelle 6), g) von der Temperatur (Tabelle 7) und h) von der Art des Elektrodenmaterials (Tabelle 8). — Es werden tensammetrische und cyclovoltammetrische Messungen durchgefuhrt. Die in trockenem Dimethylformamid erha…
The electrochemistry of carbon monoxide reductive cyclotetramerization to squarate anion
1978
Abstract The electrochemical reduction, of carbon monoxide to C4O2−4 squarate anion is investigated. Particular attention is devoted to the influence that solvents, electrolytes, electrodes and carbon monoxide pressure have on the yields. The main feature appears to be that strictly controlled conditions are not necessary for cyclotetramerization. In dmf — Bu4NBr the following yields vs reacted CO and circulated charge were obtained with different cathodes: Pt(49%, 34%); Au(48%, 29%); Al(47%, 38%); stainless steel (36%, 33%); graphite (39%, 31%). A distinct influence of the supporting electrolyte (inorganic and tetraalkylammonium halides) was however observed.
Tuning the Electrochemistry of Free-Base Porphyrins in Acidic Nonaqueous Media: Influence of Solvent, Supporting Electrolyte, and Ring Substituents
2016
International audience; A detailed study of reduction potentials, electroreduction mechanisms and acid-base chemistry was carried out on two series of free-base porphyrins in nonaqueous media. The first series is represented by four-pyrrole substituted tetraphenylporphyrin (TPP) derivatives, two of which are planar and two of which are nonplanar in their non-protonated form. The second comprises porphyrins with 0-4 meso-phenyl groups on the macrocycle. Equilibrium constants for conversion of each neutral porphyrin to its diprotic [H4P] 2+ form were determined and the electrochemistry was then elucidated as a function of: (i) type of nonaqueous solvent, (ii) anion of supporting electrolyte, …