An Effect of Bismuth Ion on the Reduction of Terbium Ion in Molten LiCl-KCl Eutectic Salt

Author(s):  
Beom Kyu Kim ◽  
Byung Gi Park ◽  
Hwa Jeong Han ◽  
Ji Hye Park ◽  
Won Ki Kim

A salt waste generated from the pyroprocess contains residual actinides and needs to be purified for recycling of the salt and waste conditioning. A co-reduction process could be considered for removal of residual actinides from the salt waste, which contains lanthanides and residual actinides. In the study, specifically, an effect of Bi(III) ion on the electrochemical reaction of Tb(III) ion was investigated in the molten LiCl-KCl eutectic with BiCl3 and TbCl3 at 773 K using electrochemical techniques of cyclic voltammetry, square wave voltammetry and open circuit chronopotentiometry. Tb(III) has a single redox couple without Bi(III). However, the cyclic voltammograms obtained at tungsten electrode in LiCl-KCl-BiCl3-TbCl3 showed four redox couples. The square wave voltammogram in same condition also showed five reduction peaks. Cyclic voltammogram and square wave voltammogram was resolved to find the accurate peaks for redox reaction. Each peak indicates the formation of Tb-Bi intermetallic compound except Tb(III) reduction peak. From the phase diagram of Tb-Bi, it is inferred that each peak corresponds to TbBi2, TbBi, Tb4Bi3, and Tb5Bi3. The open circuit chronopotentiometry was conducted to estimate Gibbs free energy of formation of Tb-Bi intermetallic compound. The experimental results obtained from three kind of the electrochemical techniques showed that Tb-Bi intermetallic compounds were electrochemically formed under potential of Tb(III) reduction potential by co-reduction of Bi(III) and Tb(III). These results indicate that underpotential deposition by co-reduction could be used for Tb(III) removal from the salt waste with Bi(III).

2007 ◽  
Vol 546-549 ◽  
pp. 571-574
Author(s):  
Xing Wu Guo ◽  
Jian Wei Chang ◽  
Shang Ming He ◽  
Peng Huai Fu ◽  
Wen Jiang Ding

The corrosion behavior of GW63 (Mg-6wt.%Gd-3wt.%Y-0.4wt.%Zr) alloys in 5% NaCl aqueous solution has been investigated by PARSTAT 2273 instrument. The Open Circuit Potential (ECORR) vs. time curve, cyclic polarization (Pitting Scans) curve and Electrochemical Impedance Spectroscopy (EIS) was measured for the GW63 alloys in as-cast and T6 heat treatment conditions. The EIS results indicated that the tendency of impedance variation for as-cast condition was monotonic decreasing, however, the tendency of variation for T6 condition was not completely monotonic but the total tendency was decreasing. The values of impedance of GW63 alloy at 0.1 Hz are about 103 ohm-cm2 for as-cast and T6 condition.


2019 ◽  
Vol 107 (2) ◽  
pp. 95-104
Author(s):  
Ru-Shan Lin ◽  
You-Qun Wang ◽  
Zhao-Kai Meng ◽  
Hui Chen ◽  
Yan-Hong Jia ◽  
...  

Abstract In this study, UCl4 was prepared by the reaction of HCl gas with UO2 in the LiCl-KCl eutectic. Then, the electrochemical behavior of U4+ and U3+ on a Mo cathode was investigated by various electrochemical techniques. The reduction process of U4+ was regarded as two steps: U4++e=U3+; U3++3e=U. Diffusion coefficients of U4+ and U3+, the apparent standard potential of U4+/U3+, U3+/U as well as U4+/U in the LiCl-KCl molten salt on the Mo electrode was determined by numerous electrochemical methods. The thermodynamic functions of formation of Gibbs free energy of UCl4 and UCl3 are calculated as well.


Author(s):  
Chan Mi Kim ◽  
In Ui Kim ◽  
S. P. Yoon ◽  
Sung Ki Cho

Abstract This study investigates the effect of MgO as an additive in molten Li2CO3-Na2CO3 electrolyte for molten carbonate fuel cells through electrochemical analyses. Addition of MgO (1~5 mol%) increased the electrochemical response in cyclic voltammogram of peroxide in molten Li2CO3-Na2CO3. The diffusion coefficient of peroxide in molten Li2CO3-Na2CO3 containing MgO was determined via the comparison between the peak currents of cyclic voltammograms from microwire electrode and macrowire electrode. The addition of MgO did not impact the diffusion coefficient, indicating that the increase in the electrochemical response with the addition of MgO might be attributed to the increase in the peroxide concentration. The change in peroxide concentration was also confirmed by electrochemical impedance analyses, which exhibited a decrease in the exchange current density. The increase in the concentration of peroxide with the addition of MgO might be associated with the high thermal decomposition constant of MgCO3, implying the high concentration of oxide ion in the molten Li2CO3-Na2CO3. This study suggests that MgO might be an effective additive for increasing the oxygen solubility in the molten Li2CO3-Na2CO3, and subsequently for enhancing the performance of molten carbonate fuel cells.


Author(s):  
Javier Espinoza-Vergara ◽  
Paulo Molina ◽  
Mariana Walter ◽  
Miguel Gulppi ◽  
Nelson Vejar ◽  
...  

The influence of pH on the electrochemical behavior of hydrogen peroxide in the presence of Pseudomonas aeruginosa was investigated using electrochemical techniques. Cyclic and square wave voltammetry were used to monitor the enzymatic activity. A modified cobalt phthalocyanine (CoPc) carbon electrode (OPG), a known catalyst for reducing O2 to H2O2, was used to detect species resulting from the enzyme activity. The electrolyte was a sterilized aqueous medium containing Mueller-Hinton (MH) broth. The open-circuit potential (OCP) of the Pseudomonas aeruginosa culture in MH decreased rapidly with time, reaching a stable state after 4 h. Peculiarities in the E / I response were observed in voltammograms conducted in less than 4 h of exposure to the culture medium. Such particular E/I responses are due to the catalase’s enzymatic action related to the conversion of hydrogen peroxide to oxygen, confirming the authors’ previous findings related to the behavior of other catalase-positive microorganisms. The enzymatic activity exhibits maximum activity at pH 7.5, assessed by the potential at which oxygen is reduced to hydrogen peroxide. At higher or lower pHs, the oxygen reduction reaction (ORR) occurs at higher overpotentials, i.e., at more negative potentials. In addition, and to assess the influence of bacterial adhesion on the electrochemical behavior, measurements of the bacterial-substrate metal interaction were performed at different pH using atomic force microscopy.


CORROSION ◽  
10.5006/0709 ◽  
2013 ◽  
Vol 69 (6) ◽  
pp. 543-550 ◽  
Author(s):  
S. Jones ◽  
K. Coley ◽  
J. Kish

When exposed to concentrated sulfuric acid, stainless steel exhibits unique electrochemical behavior. This behavior can be observed as an oscillation in open-circuit potential between the active and passive states. The transient nature of the corrosion behavior under these conditions results in a distinct challenge for measuring and predicting corrosion rates. Using a series of commercial alloys with various nickel contents, this paper outlines the utilization of electrochemical experimentation to refine the prediction of corrosion rates. The paper also discusses some of the difficulties associated with many traditional electrochemical techniques such as potentiodynamic scans when used for characterizing systems that undergo oscillations in open-circuit potential.


2020 ◽  
Vol 860 ◽  
pp. 15-21
Author(s):  
Lusi Safriani ◽  
Annisa Aprilia ◽  
Sri Suryaningsih ◽  
Fitri Yuliasari ◽  
Muhammad Rizki Nurawan ◽  
...  

The third generation of photovoltaic, called as dye-sensitized solar cells (DSSC) have attracted much attention and currently become an interesting research topics. One important part of DSSC that determines its performance is photoanodes. Recently, graphene has been used to enhance the efficiency of DSSC through the increasing of electronic transportation. Introduction of graphene into DSSC is realized by changing the form of graphene oxide (GO) into reduced graphene oxide (rGO) through the reduction process. In this work, DSSC based on TiO2 photoanodes modified by rGO were fabricated. rGO layer was deposited on TiO2 mesoporous layer using UV-oven spraying method. We found that parameters of DSSC such as open circuit voltage, short circuit current and fill factor increase with the incorporation of rGO layer in TiO2photoanodes. DSSC with TiO2/rGO photoanodes has the highest power conversion efficiency of 11.01% which contributed from the enhancement of short circuit current. The rGO layer found to be an effective layer to block charge recombination in photoanode.


2015 ◽  
Vol 7 (2) ◽  
pp. 27 ◽  
Author(s):  
Francis Tchieno ◽  
Ignas Tonle ◽  
Evangeline Njanja ◽  
Emmanuel Ngameni

We report a simple, sensitive and low-cost electrochemical procedure for the quantification of quercetin (QCT), a flavonoid and an antioxidant, based on 1-ethylpyridinium bromide modified carbon paste electrode. A 1-ethylpyridinium bromide/carbon paste composite electrode was used. The cyclic voltammogram of QCT showed two oxidation peaks at +0.575 V (vs Ag/AgCl/3M KCl) and +0.865 V (vs Ag/AgCl/3M KCl), and a reduction peak at +0.371 V (vs Ag/AgCl/3M KCl) in HCl/KCl solution at pH 1. Differential pulse voltammetry (DPV) analysis in HCl/KCl at pH 1 showed three well-defined oxidation peaks while a single peak was recorded in phosphate buffer at pH 3. The peak currents of QCT significantly increased at the 1-ethylpyridinium bromide modified electrode in comparison with those recorded at the bare carbon paste electrode. This allowed the use of adsorptive stripping voltammetry to develop a simple and sensitive electroanalytical method for the determination of QCT. Key experimental parameters such as pH of the supporting electrolyte, the preconcentration time, the electrolysis potential, electrode composition, QCT concentration and interferents were investigated. The current response was found to be directly proportional to the concentration of QCT in the range from 2.48 x 10-7 M to 7.43 x 10-6 M, leading to a detection limit of 4.48 x 10-8 M. The developed analytical method was successfully applied to the determination of QCT in human urine samples.


2014 ◽  
Vol 68 (7) ◽  
Author(s):  
Yoshihisa Kakuta ◽  
Naoyuki Masuda ◽  
Michihiro Kurushima ◽  
Takashi Hashimoto ◽  
Daisuke Yoshioka ◽  
...  

AbstractThe template reaction of salicylaldehyde and its substituted derivatives and 2-hydroxy-5-bromobenzylamine or 2-hydroxy-5-chlorobenzylamine with copper(II) acetate in dimethyl sulphoxide (dmso) afforded eight dinuclear Cu(II) complexes, [Cu2(L)2(dmso)2] (H2 L = N-salicylidene-2-hydroxy-5-bromobenzylamine, N-salicylidene-2-hydroxy-5-chlorobenzylamine and their 5-bromo, 5-nitro and 5-methyl-substituted salicylidene derivatives). These Cu(II) complexes were characterised by IR and UV-VIS-NIR spectroscopy, electric conductivity, cyclic voltammetry, and temperature dependence of magnetic susceptibilities (4.5–300 K). In the THF solution, the complexes are nonelectrolytes and exhibit a characteristic CT band due to phenoxido-bridging at 360–384 nm. In the cyclic voltammograms, an irreversible reduction process was observed at −1.18–1.54 V vs Fc/Fc+. Single-crystal X-ray crystallography revealed that two Cu(II) ions were bridged by the two phenoxido-oxygen atoms of the two Schiff-base ligands with axial coordination of dmso molecules forming a square pyramid with a Cu-Cu distance of 3.0628(8)–3.0931(6) °A. In accordance with the crystal structures, the magnetic interaction between the two Cu(II) ions is relatively anti-ferromagnetic with −2J value of 386–575 cm−1. The axial coordination effect of the dmso molecule was discussed in relation to the correlation between the Cu-O-Cu angle and the −2J value.


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