scholarly journals Ferrimicrobium acidiphilum Exchanges Electrons With a Platinum Electrode via a Cytochrome With Reduced Absorbance Maxima at 448 and 605 nm

2021 ◽  
Vol 12 ◽  
Author(s):  
Robert C. Blake ◽  
Amit Nautiyal ◽  
Kayla A. Smith ◽  
Noelle N. Walton ◽  
Brealand Pendleton ◽  
...  

Ferrimicrobium acidiphilum is a Gram-positive member of the Actinobacteria phylum that can respire aerobically or anaerobically with soluble Fe(II) or Fe(III), respectively, in sulfuric acid at pH 1.5. Cyclic voltammetry measurements using intact F. acidiphilum at pH 1.5 produced fully reversible voltammograms that were highly reproducible. The maximum current observed with the anodic peak was considerably less than was the maximum current observed with the cathodic peak. This difference was attributed to the competition between the platinum electrode and the soluble oxygen for the available electrons that were introduced by the cathodic wave into this facultative aerobic organism. The standard reduction potential of the intact organism was determined to be 786 mV vs. the standard hydrogen electrode, slightly more positive than that of 735 mV that was determined for soluble iron at pH 1.5 using the same apparatus. Chronocoulometry measurements conducted at different cell densities revealed that the intact organism remained in close proximity to the working electrode during the measurement, whereas soluble ionic iron did not. When the cyclic voltammetry of intact F. acidiphilum was monitored using an integrating cavity absorption meter, the only small changes in absorbance that were detected were consistent with the participation of a cellular cytochrome with reduced absorbance peaks at 448 and 605 nm. The cytochrome that participated in the exchange of electrons between the intact organism and extracellular solid electrodes like platinum was the same cytochrome whose oxidation was previously shown to be rate-limiting when the organism respired aerobically on extracellular soluble iron.

2000 ◽  
Vol 65 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Tomáš Loučka

The aim of this research was to study the oxidation and reduction of the adsorbed thiosulfate on the platinum electrode in a slightly alkaline medium. The adsorption was performed at the open circuit conditions. The reduction of the adsorbed layer in the hydrogen region is slower in a slightly alkaline medium than in acid. The mechanism of reduction and oxidation of adsorbed molecules is probably the same. The nonstationary currents measured in presence of thiosulfates showed that the change in the oxidation number does not take place during the adsorption in the double layer region. In the hydrogen region, thiosulfate replaces the adsorbed hydrogen while beeing reduced. Nonstationary currents at higher concentrations of thiosulfate indicate the presence of more layers on the electrode. Upon reaching higher concentrations of thiosulfate the oxidation reaction takes place between thiosulfate in solution and adsorbed product of its reduction. The open circuit potential of the platinum electrode measured in a thiosulfate solution was 0.780 and 0.783 V against the hydrogen electrode in the same solution.


2018 ◽  
Vol 34 (4) ◽  
pp. 2098-2105
Author(s):  
Raja Beryl J ◽  
Joseph Raj Xavier

Trifluoromethylation of isonicotinic acid hydrazide has been investigated in trifluoroacetic acid containing pyridine, triethylamine and sodium trifluoroacetate dissolved in acetonitrile on platinum and glassy carbon electrodes using cyclic voltammetry. LSVs for isonicotinic acid hydrazide in 0.1 M TFA/ Py/TEA/NaTFA in acetonitrile on platinum electrode show that there is no distinct oxidation peak for the oxidation of isonicotinicacid hydrazide within the voltammetric region of 0.0 to 1.6 V vs Ag and it gets oxidized anodically in the gas evolution region itself. TFA/ NaTFA medium shows slightly higher current density than the other two media for the oxidation of isonicotinic acid hydrazide. CVs for different concentrations of isonicotinic acid hydrazide show that anodic peak becomes broad and flat. It shows that severe adsorption of INAH/product takes place on the glassy carbon electrode during the voltammetry scanning. Galvanostatic electrolysis of INAH in TFA/Py/ACN medium at low current density on Pt shows good conversion with low selectivity.


2017 ◽  
Vol 14 (3) ◽  
pp. 178 ◽  
Author(s):  
Yao Luo ◽  
Yougang Shen ◽  
Lihu Liu ◽  
Jun Hong ◽  
Guohong Qiu ◽  
...  

Environmental contextDissolved sulfide results in soil acidification and subsequent contaminant leaching via oxidation processes, usually involving manganese oxides. In this work, redox processes were monitored in situ by cyclic voltammetry and HS– concentrations were semi-quantitatively determined. The method provides qualitative and semi-quantitative assessment for dissolved sulfide and its oxidation intermediates in aqueous systems. AbstractDissolved sulfide can be oxidised by manganese oxides in supergene environments, while the intermediates including S0, S2O32– and SO32– are easily oxidised by oxygen in air, resulting in some experimental errors in conventional analyses. In this work, the electrochemical behaviours of HS–, S2O32– and SO32– on a platinum electrode were studied by cyclic voltammetry and constant potential electrolysis, and in situ detection of the intermediates was conducted in aqueous systems of HS– and manganese oxides. The results showed that HS– was first oxidised to S0, and then transformed to SO42–. The peak current for the oxidation of HS– to S0 had a positive linear correlation with the used starting HS– concentration. S2O32– and SO32– were directly electrochemically oxidised to SO42–. The oxidation current peak potentials at 0, 0.45 and 0.7V were respectively observed for HS–, S2O32– and SO32– at pH 12.0. Cyclic voltammetry was conducted to monitor the redox processes of HS– and manganese oxides. The oxidation peak current of HS– to S0 decreased, and that of S2O32– to SO42– was observed to increase as the reaction proceeded. The rate of the decrease of the oxidation peak current of HS– indicated that the oxidation activity followed the order of birnessite>todorokite>manganite.


Sensor Review ◽  
2018 ◽  
Vol 38 (3) ◽  
pp. 335-344 ◽  
Author(s):  
Ilhem Ghodbane ◽  
Rochdi Kherrrat ◽  
Saida Zougar ◽  
Rim Lamari ◽  
Redouane Haddadji ◽  
...  

PurposeThe purpose of this work is to explore electrical properties of an electrochemical sensor designed for the detection of malachite green (MG) present in an aqueous solution.Design/methodology/approachThe present sensor consists in the spatial coupling of a polymeric membrane and an ion-sensitive electrode (platinum electrode). The preparation of the polymeric membrane involves the incorporation of an ionophore (D2HPA), a polymer (polyvinylchloride [PVC]) and a plasticizer (dioctyl phthalate [DOP]). Several techniques have been used to characterize this sensor: the cyclic voltammetry, the electrochemical impedance spectroscopy and the optical microscopy. The sensibility, the selectivity and the kinetic study of a modified platinum electrode have been evaluated by cyclic voltammetry.FindingsThe obtained results reveal the possibility of a linear relationship between the current of reduction peaks and MG concentration. A linear response was obtained in a wide-concentration range that stretches from 10−5to 10−13mol L−1, with a good correlation coefficient (0.976) and a good detection limit of 5.74 × 10−14mol L−1(a signal-to-noise ratio of 3). In addition, the voltammetric response of modified electrode can be enhanced by adding a layer of Nafion membrane. Under this optimal condition, a linear relationship was obtained, with a correlation coefficient of 0.986 and a detection limit of 1.92 × 10−18mol L−1.Originality/valueIn the present research, a convenient, inexpensive and reproducible method for the detection of MG was developed. The developed sensor is capable of competing against the conventional techniques in terms of speed, stability and economy.


1969 ◽  
Vol 22 (8) ◽  
pp. 1583 ◽  
Author(s):  
T Biegler

Adsorption of methanol from acid solution onto a smooth platinum electrode is studied using fast anodic potential sweeps to determine coverages. Between 0.15 and 0.6 V (against reversible hydrogen electrode) the coverage is found to be almost independent of potential. Below 0.15 V coverage measurements are unreliable because of the very slow approach to the steady state and competition for the surface by trace impurities. The results are consistent with the hypothesis that chemisorbed methanol is a stable intermediate in a sequence of irreversible oxidation stages and that the steady-stage coverage cannot be considered as a true adsorption equilibrium.


2009 ◽  
Vol 609 ◽  
pp. 249-254 ◽  
Author(s):  
K. Morakchi ◽  
A. Zazoua ◽  
A. Hamel ◽  
Saida Zougar ◽  
R. Kherrat ◽  
...  

In this work, we report the study of functionalized platinum (Pt) electrodes based on a polymeric membrane (PVC) including an ionophore (ethyln diamin tetracetic EDTA) sensitive for mercury ions Hg2+. The optimised working conditions of the sensors have been studied with regard to the sensitivity performances; in particular, the polarisation was adjusted to - 0.2V/SCE. Ion sensitivity of sensors have been tested for Hg(II) via Cd(II) in aqueous solution. A layer of EDTA deposited on platinum electrode has been characterised by impedance spectroscopy and cyclic voltammetry methods.


2021 ◽  
Vol 11 (4) ◽  
pp. 1376
Author(s):  
Bogdan Tutunaru ◽  
Adriana Samide ◽  
Simona Iordache ◽  
Cristian Tigae ◽  
Andreea Simionescu ◽  
...  

The electrochemical stability of ceftriaxone (CFTX), belonging to the third generation of cephalosporin antibiotics, was studied by electrochemical measurements recorded on a platinum electrode (Pt) in aqueous solutions containing sodium halides. The electrochemical behavior of ceftriaxone was investigated by cyclic voltammetry (CV) and constant current density electrolysis assisted by UV-Vis spectrophotometry. Cyclic voltammetry highlighted that the addition of CFTX in sodium halide solutions leads to significant changes in the hysteresis characteristics due to specific interactions with active species from electrolytes, as well as with the platinum electrode surface. After CV, when an exterior electric stimulus in short time (40 s) was applied, the UV-Vis spectra illustrated that CFTX is stable in the presence of F− ions, it is electro(degraded/transformed) in the presence of Cl− and Br− ions and interacts instantly with I− species. Electrolysis at constant current density confirms the results obtained from cyclic voltammetry, showing that (i) in the presence of fluoride ions CFTX gradually decomposes, but not completely, in about 60 min, without identifying a reaction product; (ii) chloride and bromide ions determine the almost complete CFTX electro(degradation/transformation) in 10 and 5 min, respectively, with completion of the electro-transformation reaction after 60 and 30 min, respectively; (iii) instantaneous interactions between CFTX and the iodide ions occurred.


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