Review—Concentration Measurements In Molten Chloride Salts Using Electrochemical Methods

2021 ◽  
Author(s):  
Tyler Bruce Williams ◽  
Rankin Shum ◽  
Devin Rappleye
Keyword(s):  
Electrochemical Techniques ◽  
Electrochemical Measurement ◽  
Open Circuit ◽  
Measure Concentration ◽  
Molten Chloride ◽  
Accuracy And Precision ◽  
Low Concentrations ◽  
Improve Measurement ◽  
Concentration Measurements ◽  
Chloride Salts

Abstract The electrochemical measurement of concentration in molten chloride salts is a valuable tool for the control of existing and potential industrial processes, recycling of precious materials and energy production. The electrochemical techniques commonly used to measure concentration and each techniques’ associated theory are discussed. Practices which improve measurement accuracy and precision are set forth. Exceptionally accurate and precise measurements published in the literature are evaluated based on their performance in specified concentration ranges. The strengths and weaknesses of the most accurate measurements are briefly explored. Chronopotentiometry (CP) and square wave voltammetry (SWV) are accurate and precise with low concentration measurements. SWV was accurate at low concentrations, even in multi-analyte mixtures. CP was accurate for only single analyte mixtures. Open-circuit potentiometry (OCP) is accurate and precise in single-analyte mixtures but yields large errors in multianalyte mixtures. Cyclic voltammetry (CV), chronoamperometry (CA) and normal pulse voltammetry (NPV) are accurate and precise across all concentration ranges. NPV is exceptionally well suited for measurements in melts with multiple electroactive species.

scholarly journals Thermal and Transport Properties of Molten Chloride Salts with Polarization Effect on Microstructure

Energies ◽  
2021 ◽  
Vol 14 (3) ◽  
pp. 746
Author(s):  
Jianfeng Lu ◽  
Senfeng Yang ◽  
Gechuanqi Pan ◽  
Jing Ding ◽  
Shule Liu ◽  
...  
Keyword(s):  
Heat Capacity ◽  
Polarization Effect ◽  
Chloride Salt ◽  
Coulombic Interaction ◽  
Molten Chloride ◽  
Self Diffusion ◽  
Local Structures ◽  
Property Data ◽  
Chloride Salts ◽  
And Storage

Molten chloride salt is recognized as a promising heat transfer and storage medium in concentrating solar power in recent years, but there is a serious lack for thermal property data of molten chloride salts. In this work, local structures and thermal properties for molten chloride salt—including NaCl, MgCl2, and ZnCl2—were precisely simulated by Born–Mayer–Huggins (BMH) potential in a rigid ion model (RIM) and a polarizable ion model (PIM). Compared with experimental data, distances between cations, densities, and heat capacities of molten chloride slats calculated from PIM agree remarkably better than those from RIM. The polarization effect brings an extra contribution to screen large repulsive Coulombic interaction of cation–cation, and then it makes shorter distance between cations, larger density and lower heat capacity. For NaCl, MgCl2, and ZnCl2, PIM simulation deviations of distances between cations are respectively 3.8%, 3.7%, and 0.3%. The deviations of density and heat capacity for NaCl between PIM simulation and experiments are only 0.6% and 2.2%, and those for MgCl2 and ZnCl2 are 0.7–10.7%. As the temperature rises, the distance between cations increases and the structure turns into loose state, so the density and thermal conductivity decrease, while the ionic self-diffusion coefficient increases, which also agree well with the experimental results.

Corrosion behavior of carburized 316 stainless steel in molten chloride salts

Solar Energy ◽  
2021 ◽  
Vol 223 ◽  
pp. 1-10
Author(s):  
Sen Ren ◽  
Yanjun Chen ◽  
Xiang-Xi Ye ◽  
Li Jiang ◽  
Shuai Yan ◽  
...  
Keyword(s):  
Stainless Steel ◽  
Corrosion Behavior ◽  
Molten Chloride ◽  
316 Stainless Steel ◽  
Chloride Salts

Application of Electrochemical Techniques to Characterization of the Corrosion Behaviors of GW63 Alloys

2007 ◽  
Vol 546-549 ◽  
pp. 571-574
Author(s):  
Xing Wu Guo ◽  
Jian Wei Chang ◽  
Shang Ming He ◽  
Peng Huai Fu ◽  
Wen Jiang Ding
Keyword(s):  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Open Circuit ◽  
Cyclic Polarization ◽  
Time Curve ◽  
Completely Monotonic ◽  
Treatment Conditions ◽  
Impedance Variation ◽  
Corrosion Behaviors

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.

Simultaneous quantification of vitamin E and vitamin E metabolites in equine plasma and serum using LC-MS/MS

2021 ◽  
pp. 104063872110054
Author(s):  
Hadi Habib ◽  
Carrie J. Finno ◽  
Ingrid Gennity ◽  
Gianna Favro ◽  
Erin Hales ◽  
...  
Keyword(s):  
Vitamin E ◽  
Normal Growth ◽  
Alpha Tocopherol ◽  
Limits Of Detection ◽  
Phase Gradient ◽  
Equine Plasma ◽  
Accuracy And Precision ◽  
Low Concentrations ◽  
Liquid Chromatography Tandem Mass ◽  
Acquity Uplc

Vitamin E deficiencies can impact normal growth and development in humans and animals, and assessment of circulating levels of vitamin E and its metabolites may be an important endpoint for evaluation. Development of a sensitive method to detect and quantify low concentrations of vitamin E and metabolites in biological specimens allows for a proper diagnosis for patients and animals that are deficient. We developed a method to simultaneously extract, detect, and quantify the vitamin E compounds alpha-tocopherol (α-TP), gamma-tocopherol (γ-TP), alpha-tocotrienol (α-TT), and gamma-tocotrienol (γ-TT), and the corresponding metabolites formed after β-oxidation of α-TP and γ-TP, alpha-carboxymethylbutyl hydroxychroman (α-CMBHC) and alpha- or gamma-carboxyethyl hydroxychroman (α- or γ-CEHC), respectively, from equine plasma and serum. Quantification was achieved through liquid chromatography–tandem mass spectrometry. We applied a 96-well high-throughput format using a Phenomenex Phree plate to analyze plasma and serum. Compounds were separated by using a Waters ACQUITY UPLC BEH C18 column with a reverse-phase gradient. The limits of detection for the metabolites and vitamin E compounds were 8–330 pg/mL. To validate the method, intra-day and inter-day accuracy and precision were evaluated along with limits of detection and quantification. The method was then applied to determine concentrations of these analytes in plasma and serum of horses. Alpha-TP levels were 3–6 µg/mL of matrix; the metabolites were found at much lower levels, 0.2–1.0 ng/mL of matrix.

Phenylcoumarin Glucoside as a Natural Inhibitor in the Protection of Low Carbon Steel Against Corrosion

MRS Advances ◽  
2017 ◽  
Vol 2 (62) ◽  
pp. 3909-3915
Author(s):  
Héctor M. Barbosa Cásarez ◽  
Araceli Espinoza Vázquez ◽  
Francisco J. Rodríguez-Gomez
Keyword(s):  
Carbon Steel ◽  
Inhibition Efficiency ◽  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Low Carbon Steel ◽  
Steel Corrosion ◽  
Low Carbon ◽  
Low Concentrations ◽  
Natural Inhibitor ◽  
Polarization Studies

AbstractPhenylcoumarin glucoside (4-PC) is a compound extracted from the plant Hintona latiflora and was studied as inhibitor for AISI 1018 steel corrosion in 3% NaCl solution using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques, which may find application as eco-friendly corrosion inhibitors. The 4-PC provides inhibitor properties that protect AISI 1018 low carbon steel against corrosion at low concentrations (5 ppm) obtained by EIS. Polarization studies showed that the inhibitor was of mixed type. The inhibition efficiency by the two electrochemical techniques shows similar results. The inhibitor adsorption was demonstrated to be a combined process (physisorption and chemisorption) according to the Langmuir isotherm.

scholarly journals Effect of pH on the Electrochemical Behavior of Hydrogen Peroxide in the Presence of Pseudomonas aeruginosa

2021 ◽  
Vol 9 ◽  
Author(s):  
Javier Espinoza-Vergara ◽  
Paulo Molina ◽  
Mariana Walter ◽  
Miguel Gulppi ◽  
Nelson Vejar ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Pseudomonas Aeruginosa ◽  
Enzymatic Activity ◽  
Electrochemical Behavior ◽  
Electrochemical Techniques ◽  
Stable State ◽  
Reduction Reaction ◽  
Maximum Activity ◽  
Open Circuit ◽  
Mueller Hinton

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.

Thermochemical and Experimental Kinetic Analysis of Potassium Extraction from Ultrapotassic Syenite Using Molten Chloride Salts

2019 ◽  
Vol 58 (17) ◽  
pp. 7397-7407 ◽  
Author(s):  
P. Haseli ◽  
P. Majewski ◽  
F. C. Christo ◽  
B. Hammond ◽  
F. Bruno
Keyword(s):  
Kinetic Analysis ◽  
Molten Chloride ◽  
Chloride Salts

ChemInform Abstract: Stability of YBa2Cu3O7-x in Molten Chloride Salts.

ChemInform ◽  
1990 ◽  
Vol 21 (44) ◽  
Author(s):  
C. H. RAEDER ◽  
D. B. KNORR
Keyword(s):  
Molten Chloride ◽  
Chloride Salts

Prediction and Measurement of Corrosion Rates of Stainless Steel in Concentrated Sulfuric Acid

CORROSION ◽  
10.5006/0709 ◽  
2013 ◽  
Vol 69 (6) ◽  
pp. 543-550 ◽  
Author(s):  
S. Jones ◽  
K. Coley ◽  
J. Kish
Keyword(s):  
Stainless Steel ◽  
Sulfuric Acid ◽  
Corrosion Behavior ◽  
Electrochemical Behavior ◽  
Open Circuit Potential ◽  
Electrochemical Techniques ◽  
Open Circuit ◽  
Corrosion Rates ◽  
Transient Nature ◽  
Concentrated Sulfuric Acid

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.

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