On the use of electrochemical techniques to monitor free oxide content in molten fluoride media

The electrochemical behaviour of oxide ions has been studied in fluoride melts(LiF/NaF eutectic) by cyclic voltammetry, square wave voltammetry and chronopotentiometry. The purpose is to determine whether these techniques can be used for titration of free oxide ions (O2-) in molten fluorides released by lithium oxide additions. Cyclic voltammetry is shown to be unsuitable for this purpose due to oxygen bubbling disturbing the oxidation peak, while square wave voltammetry is far more appropriate because the observed signal is a well defined oxidation peak with a height proportional to the oxide content. Thus, the present work is focused on a strategy of oxide ions titration by square wave voltammetry. In addition, this work allows assessing that the electrochemical reduction of oxide ions proceeds by diffusion of these species, and the O2- diffusion coefficient is estimated by chronopotentiometry

Opportunities for mesoporous nanocrystalline SnO2 electrodes in kinetic and catalytic analyses of redox proteins

PFV (protein film voltammetry) allows kinetic analysis of redox and coupled-chemical events. However, the voltammograms report on the electron transfer through a flow of electrical current such that simultaneous spectroscopy is required for chemical insights into the species involved. Mesoporous nanocrystalline SnO2 electrodes provide opportunities for such ‘spectroelectrochemical’ analyses through their high surface area and optical transparency at visible wavelengths. Here, we illustrate kinetic and mechanistic insights that may be afforded by working with such electrodes through studies of Escherichia coli NrfA, a pentahaem cytochrome with nitrite and nitric oxide reductase activities. In addition, we demonstrate that the ability to characterize electrocatalytically active protein films by MCD (magnetic circular dichroism) spectroscopy is an advance that should ultimately assist our efforts to resolve catalytic intermediates in many redox enzymes

An Overview of Carbon Fiber Electrodes Used in Neurochemical Monitoring

Neurochemistry has always been a topic that many scientists are interested in researching because the brain is such a fascinating and complex organ. Electrochemical methods have proven to be a successful tool for scientists to use for their brain-researching endeavors. Many types of probes and analytical devices have been invented and used in conjunction with electrochemical methods over the past several decades to investigate the inner workings of the brain. In particular, the carbon fiber electrode has become a popular device among scientists due to its favorable qualities.The carbon fiber electrode has several unique characteristics to give it an advantage over other techniques. Carbon fiber electrodes have the ability to monitor in a subsecond time frame and record in real time. Because they are so small, carbon fiber electrodes are also able to sample very small environments, such as a single cell or vesicular volumes, where other devices cannot because they are too big. Evidence has shown that carbon fiber electrodes appear to cause less disruptive tissue damage when implanted into a brain than other devices, for instance a microdialysis probe. On top of that, carbon fiber electrodes are also excellent devices for those seeking greater sensitivity and selectivity by making electrode modifications tailored for the analyte of interest. In addition, carbon fiber electrodes provide a wider range of detectable species, again by simply making slight modifications. One can clearly see that the future for neurochemical monitoring lies heavily in the hands of the carbon fiber electrode. Its advantages over other devices make it superior in many aspects. Researchers will no doubt continue to use the carbon fiber electrode and keep improving it to make it suitable for countless more experiments

Voltammetry at porous electrodes: A theoretical study

Theory is presented to simulate both chronoamperometry and cyclic voltammetry at porous electrodes fabricated by means of electro-deposition around spherical templates. A theoretical method to extract heterogeneous rate constants for quasireversible and irreversible systems is proposed by the approximation of decoupling of the diffusion within the porous electrode and of bulk diffusion to the electrode surface

Electrochemical study of the Eu(III)/Eu(II) system in molten fluoride media

The electrochemical behaviour of the Eu(III)/Eu(II) system was examined in the molten eutectic LiF-CaF2 on a molybdenum electrode, using cyclic voltammetry, square-wave voltammetry and chronopotentiometry. It was observed that EuF3 is partly reduced into EuF2 at the operating temperatures (1073-1143 K). The electrochemical study allowed to calculate both the equilibrium constant and the formal standard potential of the Eu(III)/Eu(II) system. The reaction is limited by the diffusion of the species in the solution; their diffusion coefficients were calculated at different temperatures and the values obey Arrhenius' law. The second system Eu(II)/Eu takes place out of the electrochemical window on an inert molybdenum electrode, which inhibits the extraction of Eu species from the salt on such a substrate

The Electrochemical Oxidation of Organic Selenides and Selenoxides

The electrochemical oxidation of alkyl and aryl selenides was investigated in acetonitrile. The oxidation of diphenyl selenide and di(4‐methylphenyl) selenide led primarily to the formation of their respective selenoxides, which were identified by exhaustive coulometric oxidation and and analysis of the products. The selenoxide itself was not observed in the cyclic voltammetry of the selenide for two reasons: first, the protonation of the selenoxide by the acid formed from the reaction of water with the cation radical and second, the formation of a selenoxide hydrate. The formation of the hydrate with diphenyl selenoxide was verified by isolation of the dimethoxy derivative. In addition to the selenoxide, selenonium compounds, formed by the coupling of the oxidized material, were also observed. The alkyl selenides were generally oxidized at a lower potential than the aryl selenides. This trend is different from the sulfur analogues, where the aryl sulfides are easier to oxidize than their alkyl counterparts. As a result, the difference in their redox potentials is relatively small. These differences may occur because the oxidation of aryl sulfides is more likely to take place on the aromatic ring, which leads to a greater yield of the coupled products (about 100%) when compared to the selenide analogue

Serotonin, how to find it...

Serotonin or 5-hydroxytryptamine (5-HT) is a monoamine neurotransmitter. Biochemically derived from tryptophan, serotonin is primarily found in the gastrointestinal tract, platelets, and in the central nervous system (CNS) of animals, including humans. Discovered and crystallized over sixty years ago, serotonin operates as a short-range neurotransmitter as well as a long-range signalling modulator, with multiple effects on whole organism functions via plasma, platelet and neuroendocrine, gut, adrenal and other peripheral systems across many species. All of the important functions of serotonin in the brain and body were identified over the ensuing years by neurochemical, physiological and pharmacological investigations. Mainly, all these investigations have been performed via invasive methodologies, particularly in the CNS studies. Here we present a rapid overview of such methodological approaches focussing on voltammetry, one of the most recent technical approaches for serotonin analysis in vivo, in situ and in real time. Furthermore, we introduce a late technical evolution in the attempt to obtain in vivo non invasive measurement of brain serotonin.peer-reviewe

Iron redox pathway revealed in ferritin via electron transfer analysis.

Ferritin protein is involved in biological tissues in the storage and management of iron - an essential micro-nutrient in the majority of living systems. While there are extensive studies on iron-loaded ferritin, its functionality in iron delivery is not completely clear. Here, for the first time, differential pulse voltammetry (DPV) has been successfully adapted to address the challenge of resolving a cascade of fast and co-occurring redox steps in enzymatic systems such as ferritin. Using DPV, comparative analysis of ferritins from two evolutionary-distant organisms has allowed us to propose a stepwise resolution for the complex mix of concurrent redox steps that is inherent to ferritins and to fine-tune the structure-function relationship of each redox step. Indeed, the cyclic conversion between Fe3+ and Fe2+ as well as the different oxidative steps of the various ferroxidase centers already known in ferritins were successfully discriminated, bringing new evidence that both the 3-fold and 4-fold channels can be functional in ferritin