Evaluation of the Electrochemical Behavior of CeCl3 in Molten LiCl-KCl Eutectic Utilizing Metallic Ce as an Anode

Marsden, K. C.; Pešić, Batrić

doi:10.1149/1.3575637

Cited by 74 publications

(52 citation statements)

References 33 publications

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“…In most of the studies, measurements have been made simply by visual determination of the immersion depth, 4,14,17,[22][23][24][25][26][27][28]32,33,39,42,[49][50][51][52][53]58 which has an error associated with capillary effects and wetting between the electrode and the salt at different temperatures. Several studies used wires encased in alumina or other insulating material tubes with a known apparent surface area.…”

Section: Resultsmentioning

confidence: 99%

Method Development for Quantitative Analysis of Actinides in Molten Salts

Tylka

Willit

Prakash

et al. 2015

J. Electrochem. Soc.

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This paper describes how electrochemical techniques have been used to develop a method for high-precision, real-time quantitative measurements of the concentration of actinides, present in in molten salts as actinide chlorides, for pyrochemical process monitoring applications. Possible reasons for discrepancies between reported measurements obtained with electrochemical techniques have been investigated and a combination of methods to improve their precision has been established. The combination of methods consists of selecting a suitable electroanalytical measurement technique, experimentally verifying assumptions used in its theoretical analysis, ensuring reproducible conditions at the electrode/electrolyte interface, and using an improved method to eliminate the need to know the electrode surface area. By following the developed procedures and refining both experimental techniques and data analysis methods, precise and reproducible measurements were obtained for U and Pu in LiCl/KCl eutectic at 773 K. Preliminary results showed that cyclic voltammetry, along with a method of standard area addition, are very promising tools for in situ quantitative measurements with a degree of precision comparable to destructive analysis techniques. Electrorefining is the main step in pyrochemical reprocessing. During this process, actinides are separated from the bulk of the fission product elements by electrochemical dissolution and electrotransport onto a solid or liquid cathode. The goal of the process is to maximize the separation and recovery of actinides from chlorinated fission products so that minimal amounts of actinides are lost to the process waste stream. [1][2][3][4][5] In addition to efficient actinide recovery, there is a need to address the safeguarding the recycle system. 5 Highprecision, real-time concentration measurements of actinides, present as actinide chlorides, in molten salts are required for process monitoring and control and could be used to support traditional material control and accountability techniques. Development of these measurements is essential to implement and operate a commercial fuel reprocessing facility. [6][7][8][9][10] Electrochemical techniques are well suited for in situ monitoring because they allow rapid, real-time measurements, are compatible with remote handling operations, and do not require the use of standards. Also, the equipment is not affected by the high radiation field present in a fuel processing operation.9,10 Unlike offline destructive analysis techniques, in situ methods do not require representative sample collection and preparation, and therefore avoid problems with sample contamination and degradation. In addition, analytical results can be received in a relatively short period (for example, less than 2 minutes).In an electrochemical cell, the measured potential (E), current (i), or charge (Q) is related to the quantity of the analyte in the solution; therefore, it can serve as an analytical signal for concentration measurements. 11,12 Depending on the applied...

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Section: Resultsmentioning

confidence: 99%

Method Development for Quantitative Analysis of Actinides in Molten Salts

Tylka

Willit

Prakash

et al. 2015

J. Electrochem. Soc.

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“…On the contrary, there have been many quantitative studies completed for the electrodeposition of lanthanide elements (Er, Ce, Tb, Gd, etc.). Both, A-S and S-H theoretical models have been used to study the electrodeposition of cerium (Ce 3+ /Ce 0 ), 22 26 reported, in CV studies of LiCl-KCl-ErCl 3 on a tungsten electrode, an observable "crossover" between the positive and negative scan curves. The reason for this behavior has been linked to the difference between the potential required for the formation of stable nuclei on an inert surface…”

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confidence: 99%

Electrochemical Nucleation and Growth of Uranium and Plutonium from Molten Salts

Tylka¹,

Willit²,

Williamson³

2017

J. Electrochem. Soc.

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This work examines the nucleation and growth behavior of uranium and plutonium from molten LiCl-KCl eutectic on inert electrodes using electrochemical techniques. Current-time transients obtained from chronoamperometric experiments were compared with theoretical models to characterize the type of nucleation (progressive or instantaneous) for deposition of U and Pu, and co-deposition of U-Pu, from molten LiCl-KCl at inert electrodes. It was established that the nucleation mode of actinides present as chlorides in molten chloride salts changes from progressive to instantaneous with an increasing concentration of the trivalent actinide ions in the salt. The effect of the material of the working electrode was investigated, and it was found that changing the material from tungsten to silver improves resolvability of the nucleation peaks and allows more accurate analysis of the experimental measurements. Using the nucleation data, diffusion coefficients were obtained for U 3+ and Pu 3+ , and were found to be in very good agreement with the values obtained from other studies. The density of nuclei produced during instantaneous nucleation, the rate of nucleation for progressive nucleation, and the radius of the deposited nuclei were evaluated and examined at different overpotentials. Pyrochemical reprocessing technology represents a promising alternative to aqueous processes for separating actinides from irradiated fuel by applying electrolytic methods to the molten salt media. [1][2][3][4][5][6][7] Electrorefining is the main step in pyrochemical reprocessing. During this process, actinides are separated from the bulk of the fission product elements by electrotransport onto a solid or liquid cathode. Electrochemical deposition that takes place at the electrode/electrolyte interface occurs by a process of nucleation and growth and is strongly dependent on the overpotential. [8][9][10][11] Nuclei initially form at active sites of the substrate, consistent with some nucleation rate law, and then grow via the incorporation of additional ions from the electrolyte. Determination of the fundamental parameters of the nucleation and growth phenomena and a very good physical understanding of these processes are essential for improved control and efficiency of pyroprocesses.Electrochemical methods are widely used to study nucleation and growth phenomena in aqueous or molten media because the driving force of nucleation can be easily changed by varying the applied potential.12 Chronoamperometry (CA) is the most frequently used technique for quantitative analysis of the deposition process; it entails applying potential step pulses and observing the resulting currenttime transients. Immediately after applying the potential step, there is a decreasing current transient corresponding to the charging of the double layer, followed by a current due to the formation of the new phase, and an increase in the number of nuclei. As the nuclei grow, the coalescence of adjacent diffusion zones gives rise to a current maximum, followed by a decay...

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“…The cost of instrumentation is relatively low, thus inexpensive [25], and some of these techniques like stripping voltammetry are highly sensitive [26] and selective which can be used up to ppm and ppb level determinations [27]. Therefore, stripping voltammetry is a promising technique for the determination of palladium in high level nuclear waste since dealing with the least amount of nuclear materials is also important because of the radioactivity issue [28].…”

Section: Introductionmentioning

confidence: 99%