Search results for " electrolyte"
showing 10 items of 106 documents
Speciation of chitosan with low and high molecular weight carboxylates in aqueous solution
2009
Quantitative data on the speciation of chitosan (310 kDa) with low and high molecular weight carboxylates in aqueous solution are reported. The following carboxylic ligands were considered: monocarboxylate (butyrate); dicarboxylates (malonate, succinate, azelate); tricarboxylate (1,2,3-propa- netricarboxylate); tetracarboxylate (1,2,3,4-butanetetracarboxylate); polyacrylates (2.0 and 20 kDa); polymethacrylate (5.4 kDa). The investigation was performed by potentiometry at t 1/4 25 C, at low ionic strength (without addition of supporting electrolyte) and at I 1/4 0:15 mol L 1 (NaCl). For all the systems the formation of (chitosan)LHi species was found (L 1/4 carboxylic ligand; i 1/4 1 to 4 de…
ELECTROCHEMICAL CONVERSION OF DICHLOROACETIC ACID TO CHLOROACETIC ACID IN A MICROFLUIDIC STACK AND IN A SERIES OF MICROFLUIDIC REACTORS
2015
The electrochemical conversion of dichloroacetic acid to chloracetic acid was performed in three different micro devices: a simple micro fluidic cell; a microfluidic stack equipped with various electrode chambers in series and three micro fluidic cells in series. The electrochemical synthesis of chloracetic acid was performed successfully with high yields and selectivity under a single-pass mode without supporting electrolyte at low cell voltages. An increase of the productivity and of the final concentration of the target product was achieved by using a stack with two or three electrode chambers in series. The utilization of three micro reactors in series open interesting new perspectives,…
Metal-free electrochemical fluorodecarboxylation of aryloxyacetic acids to fluoromethyl aryl ethers
2020
Electrochemical decarboxylation of aryloxyacetic acids followed by fluorination provides easy access to fluoromethyl aryl ethers. This electrochemical fluorodecarboxylation offers a sustainable approach with electric current as traceless oxidant. Using Et3N·5HF as fluoride source and as supporting electrolyte, this simple electrosynthesis affords various fluoromethoxyarenes in yields up to 85%.
Abatement of Acid Orange 7 in macro and micro reactors. Effect of the electrocatalytic route
2014
Abstract The electrochemical treatment of aqueous solutions contaminated by Acid Orange 7 (AO7) was widely studied with the main objective to evaluate as the electrocatalytic route affects the performances of the degradation process in macro and microfluidic cells. Direct anodic oxidation (EO), electro-Fenton (EF), electro-generation of active chlorine (IOAC) and coupled processes were investigated in macro and microfluidic reactors in order to select more effective conditions for the treatment of such compound. The effect of numerous operative parameters (such as nature of the electrode materials, coupling of processes, flow rate, current density and inter-electrode distance) on the perfor…
Determination of rate constants of ion transfer kinetics across immiscible electrolyte solutions
1998
Abstract The rotating diffusion cell was used to study ion transfer across the interface between two immiscible electrolyte solutions. Tetrabutylammonium was chosen as the transferring cation and lithium chloride as the supporting electrolyte in aqueous phase. Tetrabutylammonium tetrakis-(4-fluorophenyl)-borate in 2-nitrophenyl-octylether was used as the organic electrolyte solution supported in the porous membrane. The quasi-steady state current–voltage curves were measured both by applying potential steps and by imposing a slow potential sweep. The analysis of experimental results was based on the comparison with the theoretical current–voltage curves and on the Koutecky–Levich plots. The…
A stacked interleaved DC-DC buck converter for proton exchange membrane electrolyzer applications: Design and experimental validation
2019
Abstract Since the two last decades, hydrogen production has been attracting the attention of the scientific community thanks to its inherent very low pollution when energy coming from renewable energy sources (RESs) are used. However, it implies the use of DC/DC converters to interface source and load. These conversion systems must meet several requirements from current ripple point of view, energy efficiency, and performance to preserve the sustainability of hydrogen production. This article proposes the design and realization of a stacked interleaved buck converter to supply a proton exchange membrane electrolyzer. The converter is designed to ensure a low output current ripple and a sui…
Generalization of a finite-difference numerical method for the steady-state and transient solutions of the nernst—planck flux equations
1985
Abstract A generalization of the numerical method of Brumleve and Buck for the solution of Nernst—Planck equations when convective flux and electric current are involved has been developed. The simulation procedure was applied to a specific case: transport of strong electrolytes in a wide-pore membrane with simultaneous diffusion, convection and electric current. Good agreement was found between experimental data and computed results.
Cathodic reduction of hexavalent chromium coupled with electricity generation achieved by reverse-electrodialysis processes using salinity gradients
2014
Abstract A new approach for the simultaneous generation of electric energy and the treatment of waters contaminated by recalcitrant pollutants using salinity gradients was proposed. Reverse electrodialysis allows for the generation of electric energy from salinity gradients. Indeed, the utilization of different salt concentrations gives a potential difference between the electrodes which allows the generation of electric energy by using suitable electrolytes and an external circuit. The simultaneous generation of electric energy and the treatment of waters contaminated by Cr(VI) was successfully achieved for the first time by reverse electrodialysis processes using salinity gradients and pr…
Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
2019
Abstract We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.
Electrochemical impedance spectroscopy of thin films with two mobile charge carriers: effects of the interfacial charging
1999
In the electrochemical systems containing an excess of the background electrolyte, the faradaic process and the interfacial (‘double-layer’) charging are coupled to the fluxes of different charge carriers, the former being related to the diffusional transport of electroactive entities while the latter being realized mostly by ions of the supporting electrolyte. As a result, the interfacial capacitance Cdl may simply be added in parallel to the faradaic impedance specific for each particular system (Randles & Ershler). This simple treatment is not justified in the absence of an indifferent electrolyte, if the same charged species take part in both the electrode reaction and the double layer …