Interaction of Mn(II) and Zn(II) with ciprofloxacin antibiotics

The aim of this study is to check the redox behavior of Mn (II) and Zn (II) metals before and after interaction with ciprofloxacin in potassium chloride solution by using cyclic voltammetry, chronoamperomety and chronocoulometry methods. Equimolar solutions of Mn (II) and ciprofloxacin were mixed to a ratio of 1:2 and that of Zn (II) and ciprofloxacin to a 1:1 ratio. The results showed that the redox couple involved in Mn (II) as well as Mn(II)-ciprofloxacin interaction systems are quasi-reversible. However, the Zn (II) systems showed reversibility and the Zn(II)-ciprofloxacin interaction was quasi-reversible. The results obtained from the chronoamperometric study showed that after interaction with ciprofloxacin the rate of electrolysis in the metal systems decreased. Bangladesh J. Sci. Ind. Res.56(4), 285-292, 2021

Standard rate constants of charge transfer for the redox couple Ti(IV)/Ti(III) in chloride-fluoride melts with the different cationic composition

The influence of the second coordination sphere of titanium complexes on the charge transfer kinetics of the Ti (IV)/Ti (III) redox couple in melts of alkali metal halides was studied by cyclic voltammetry method. Diffusion coefficients in the CsC-CsF (10 wt. %) melt were calculated. The standard rate constants of charge transfer have been determined by the Nicholson method. The activation energies of the charge transfer process in (NaCl- KCl)equimol-NaF (10 wt. %) — K2TiF6, KCl-KF (10 wt. %) — K2TiF6 and CsCl-CsF (10 wt. %) — K2TiF6 melts were calculated.

Electrochemical Study of Butyl-Pyrene Nitrobenzoate Derivatives Trapped on MWCNT Nanostructured Electrodes

In the scope of our studies tending to find new nanostructured electrodic platforms containing nitroaromatic compounds (NACs) capable of generating in situ electrocatalytic redox couples, we synthesized and electrochemically studied three related 4-(pyren-1-yl)-butyl-substituted nitrobenzoates (2-NBPy, 3-NBPy and 4-NBPy). The design of the compounds is based on a combination of a) an adsorptive tail (-butyl-pyrene) capable of interacting via π-π stacking with the MWCNT nanostructured electrodes and b) nitroaromatic compounds (NACs) capable of electrochemically activating to form a RNHOH/NO redox couple trapped on the nanostructured electrodic platform. Morphological and structural analyses of the nanostructured interfaces were performed by SEM and WAXS/SAXS analysis. All of the NBPy compounds trapped on the nanostructured electrodic platform were susceptible to reduction, generating the corresponding hydroxylamine derivative. The order of ease of reduction for the nitrocompounds is 4-NBPy > 2-NBPy > 3-NBPy. After electrochemical activation, all compounds generated an RNHOH/NO redox mediator couple with the following order of stability of the mediator couple: 2-NBPy > 3-NBPy > 4-NBPy. For the 2-NBPy and 3-NBPy derivatives, excellent stability of the couple was observed, and a decrease in the peak current of 6% was observed after 60 minutes.

Some thermodynamic and kinetic properties of H2SO4–H3PO4–H2O–Fe(III) system

The values of the electrode potentials of the redox couple Fe(III) / Fe(II) and the half-wave potentials of the reactions Fe3+ + e– = Fe2+ и Fe2+ — e– = Fe3+ on the cyclic voltammogram of a platinum electrode in acid solutions containing Fe(III) salts have been measured to characterize the oxidizing ability of the H2SO4—H3PO4—H2O—Fe(III) system. The values of these experimentally obtained parameters are close. A decrease in the oxidizing ability of H2SO4 and H3PO4 mixtures containing Fe(III) with an increase in the molar fraction of H3PO4 in them occurs due to the formation of Fe(III) complexes with phosphate anions which are inferior to their hydrate and sulfate complexes in the oxidizing ability. The temperature coefficients of the electrode potential (dE / dt) of the redox couple Fe(III) / Fe(II) in the H2SO4—H2O, H2SO4—H3PO4—H2O and H3PO4–H2O systems were determined experimentally. The diffusion coefficients of Fe(III) in the studied solutions were calculated based on the Randles—Shevchik equation. The temperature dependence of the diffusion coefficients of Fe(III) cations is satisfactorily described by the Arrhenius equation. The parameters of this equation are calculated.

The Use of Nanostructured Calcium Silicate in Solar Cells

<p>Nanostructured calcium silicate (NCaSil) had previously been found to be photoactive and mildly semiconducting. Its use in solar cells was investigated in this project. Many different types of solar cells exist. Most common on the market are silicon-based cells, which generate charge separation through electric fields at p/n junctions. Over the last decade, dye-sensitised solar cells (DSSCs) have been heavily researched. DSSCs depend on effective electron/hole separation at the dye and efficient transfer to the electron- and hole-conducting materials. An older and little-researched form of cells is the photogalvanic cell, of which there are two forms. One contains a semiconducting material, whereas the other comprises of either one or two redox couples, in which at least one species is photoactive. An example of the latter form of cell is the odide/triiodide redox couple, which is commonly the electrolyte of choice in DSSCs and semiconductor-containing photogalvanic cells. This project predominantly investigated the use of NCaSil in conjunction with the iodide/triiodide redox couple and its use in solar cells. The project ascertained that, when used with the iodide/triiodide, the NCaSil did not act as a semiconducting material (either as in a DSSC or semiconductor photogalvanic cell). Rather iodide/triiodide's photogalvanic process dominated the cell, despite the presence of NCaSil. Furthermore, the addition of the stable NCaSils to the iodide/triiodide (with 5 wt% CaCl2) created "soggy sand electrolytes". These electrolytes showed increased conductivities, despite their higher viscosities, due to a synergistic effect. Soggy sand electrolytes show great promise in the development of more solid-like DSSCs. Furthermore, the project observed that the performance of NCaSil cells was maximized with a 70 wt% ethanol (30 wt% water) solvated electrolyte, with 1.5 wt% CaCl2 added to this electrolyte (or 5 wt % CaCl2 in the water content). When used long-term in conjunction with Reinforced NCaSil, a gel was formed, which showed promising activity. This activity was attributed to the interaction of surface-bound Ca2+ to iodine. Similar gels formed from vanadium- and cerium-treated NCaSil also showed great cell performance. Cell performance was further enhanced by backing the cell with a reflective or light scattering material, such as Teflon tape.</p>