Electrolyte Concentration Research Articles

Effect of changes in organo-silicon electrolyte concentration and composition on SiO2 ceramic coating prepared by plasma electrolytic oxidation on 6061 aluminum alloy

An amorphous SiO2 ceramic coating with a thickness of ∼72 μm is prepared within 13 min in organo-silicon electrolyte, which is stable in strong acid solutions, reducing corrosion current density of 6061 aluminum alloy by 3 orders of magnitude. With the aim to reveal influence of the electrolyte concentration, NaOH content and additive (NaPO3)6 on microstructure and corrosion resistance of the coatings, SEM/EDS, XRD, electrochemical tests were used to characterize their thickness, surface and cross-sectional morphology and structure, and corrosion performance prepared by using different electrolytes under the same electric control parameters. The results show that they significantly affect the surface morphology, structure and corrosion resistance of the coatings. Dilution of the electrolyte results in a significant decrease in coating thickness and surface porosity, reduction of NaOH content leads to coating thinning, increased porosity but reduced pore size. Coatings with lower porosity or smaller pore sizes are more effective in resisting corrosive media penetration for long term immersion. Whereas, the additive (NaPO3)6 promotes coating thickening, widening of the transition layer, which helpfully improves the corrosion resistance of the coating.

Study on the efficacy and mechanism of treatment of manganese-containing wastewater by pulse-alternating current coagulation

ABSTRACT To assess the effectiveness and underlying mechanism of pulse-alternating current coagulation (PACC) for treating manganese-laden wastewater, we examined the influence of various parameters. Specifically, we investigated the impact of current density, initial pH, initial Mn2+ concentration, electrolyte concentration, and alternating current frequency on the removal efficacy. The removal mechanism was meticulously examined using an adsorption kinetics analysis, Scanning Electron Microscope (SEM), Energy Dispersive Spectroscopy (EDS), Fourier Transform Infrared Spectrum (FTIR), and X-ray Photoelectron Spectroscopy (XPS). The findings indicated that the concentration of Re (Mn2+) was 99.09% under the specified conditions: j = 2.5 A·m−2, pH0 = 7, c 0(Mn2+) = 50 mg·dm−3, f = 500 Hz, c 0(NaCl) = 500 mg·dm−3 and t = 40 min. When Re (Mn2+) = 98%, the energy consumption (EEC) was significantly lower for PACC at 1.23 kWh·m−3, compared to 1.52 kWh·m−3 for direct current condensation (DCC). This indicated a reduction in EEC by 19.1% when using PACC over DCC. The adsorption process of Mn2+ by the iron sol adheres to the principles of pseudo-second order kinetics. The primary component of flocs generated in the PACC process is α-FeOOH. The mechanism of Mn2+ removal in the PACC process involved the synthesis of Mn oxides, the formation of metal hydroxide precipitates and adsorption by nano-iron sol. This study provides a theoretical basis and technical support for the application of PACC technology in the field of manganese-containing wastewater treatment.

Decrease in electrolyte after vitrectomy surgery may affect the results of forensic investigations using vitreous humor

PurposeVitreous humor (VH) is used for postmortem biochemical studies because it is well protected in an uncontaminated state even after death. The goal of this research was to investigate electrolyte concentrations in the VH from human eyes with and without a history of vitrectomy surgery.MethodsWe analyzed the sodium (Na), potassium (K), chloride (Cl) and magnesium (Mg) concentrations from 34 VH samples from 34 patients. Eleven samples were from eyes with a history of vitrectomy, and the remaining 23 eyes had no history of vitrectomy. The correlations of Na, K, Cl and Mg concentrations with patient age, interval between first and second vitrectomy, and lens status (history of cataract surgery) were also evaluated.ResultsThe Na, K, Cl and Mg concentrations in VH from vitrectomized eyes were 134.1 ± 7.9 mmol/L, 3.7 ± 0.2 mmol/L, 99.7 ± 6.7 mmol/L and 0.59 ± 0.09 mmol/L, respectively; all were significantly lower than the corresponding concentrations in VH from control eyes (lower by 5.0%, 11.0%, 11.7%, and 22.6%, respectively). Na, K, Cl and Mg concentrations in VH from vitrectomized eyes did not show significant correlations with patient ages or the interval between their first and second vitrectomies. There were no significant differences in Na, K, Cl and Mg concentrations in VH between phakic eyes and intraocular lens-implanted eyes.ConclusionsWith the increasing number of vitrectomies being performed, it is necessary to consider the history of vitrectomy when using a subject’s VH in forensic examination.

Anion‐Derived Solid Electrolyte Interphase Enabled by Diluent Modulated Dimethyl Carbonate‐Based Localized High Concentration Electrolytes for Lithium Metal Batteries

AbstractCarbonate‐based electrolytes generally suffer from low Coulombic efficiency and poor cycling stability in lithium metal batteries. In this work, localized high concentration electrolytes (LHCEs) based on dimethyl carbonate (DMC) with varying diluent additions are designed. LHCEs demonstrate higher Li+ transference numbers and a greater proportion of contact ion pairs (CIPs) and ion pair aggregates (AGGs) in the solvation structures, facilitating the formation of anion‐derived solid electrolyte interphase (SEI). Furthermore, LHCEs enhance the Coulombic efficiency of Li||Cu cells and improve the anodic stability against lithium. One of these LHCEs, prepared with appropriate diluent addition, exhibits excellent capacity retention in Li||NCM622 cells at 0.5 C after 150 cycles, thus presenting promising possibilities for the development of high energy density lithium metal batteries.

Dynamics of Urine Electrolytes in Term Neonates during the 1st Week of Life

Background: Urine electrolyte assessment is vital for diagnosing and managing neonatal conditions. However, the challenge of urine collection in neonates has resulted in a lack of standardized urine electrolyte reference values. Aim: This study seeks to explore the reference levels and potential trends in serum and urine electrolytes to better understand how the kidneys handle these substances. Methods: Healthy neonates were prospectively enrolled following normal births. Using biochemical methods, blood and urine samples were collected and analyzed on the 1st and 5th postnatal days. Statistical analysis was performed using descriptive statistics and the Wilcoxon matched-pairs signed-rank test. Results: This prospective study enrolled 55 healthy neonates. Significant changes in serum electrolyte concentrations were observed between the 1st and 5th days after birth. Notably, sodium, creatinine, urea nitrogen, and uric acid levels decreased, whereas potassium, calcium, and phosphate levels increased. Urine analysis revealed significant increases in the tubular maximum phosphate reabsorption per glomerular filtration rate and decreases in the fractional excretion of potassium and uric acid by Day 5. Conclusion: This study challenges prevailing assumptions about the stability of neonatal urine electrolytes and highlights dynamic changes in the first postnatal week. These insights lay the groundwork for further research into electrolyte disorders in newborns and have potential implications for improving neonatal care practices.

Detailed characterizations of proton permeability properties through commercial Nafion® films under various acidic electrolytes

Nafion® film has been widely used as a representative cationic ion exchange membrane for electrochemical systems including water splitting. However, detailed H+ permeability properties have been poorly understood thus far. We here attempt to relate the H+ permeability with the material properties of Nafion® films. For that, four samples representing two casting types were selected to study the H+ permeability. We conducted the pretreatment to see the effect of the new alignment of the water clusters on the H+ permeability. Although the studied membranes show individual transport features, we observed the increased H+ permeability from 0.05 to 0.5 M concentrations in acidic electrolytes. Such a feature is caused by the increased chemical-potential gradient along with the osmotic de-swelling. We also found that a H+ diffusion channel is associated with the ionic cluster size of the films, which can explain the higher H+ permeability after the pretreatment. Lastly, the individual H+ permeability was obtained when measuring at different electrolytes, revealing that the H+ permeability is strongly influenced by the anionic mobility rather than the acidic dissociation constants. Our results provide a fundamental understanding of the H+ transports through the commercial Nafion® membrane, which gives a guideline for the rational design of ion exchange membranes.

A study on soil aggregate stability and splash erosion under exogenous electrolyte conditions in the karst region of Southwest China

Study areaKarst region in Guangxi Province, Southwest China. Study focusBoth soil properties and rainfall characteristics have a critical influence on splash erosion and aggregate stability. However, the impact of electrolytes on splash erosion has received less attention. In this study, soils from 4 typical land use types (cropland, orchard, artificial forest and secondary forest) in karst region were utilized as the research objects. NaCl, KCl, and MgCl2 solutions of different concentrations were used to determine the stability of the aggregates via fast wetting (FW) treatment of Le Bissonnais (LB) method and the characteristics of splash erosion via simulated rainfall experiments. New hydrological insights for the regionResults revealed that both the land use types and electrolyte significantly influenced the soil aggregate stability and splash characteristics. Specifically, the change in land use from cropland to orchard, artificial forest and secondary forest significantly increased the aggregate stability, thus decreasing soil erodibility. The aggregate stability decreased and the total splash rate increased as the electrolyte concentration increased. The total splash erosion rate of the 4 soils was positively correlated with the <0.5 mm particle size released by aggregate fragmentation under simulated rainfall conditions. The results can provide a theoretical basis for soil erosion control and soil quality improvement in the karst region of Southwest China.

Double-Salts Super Concentrated Carbonate Electrolyte Boosting Electrochemical Performance of Ni-Rich LiNi0.90Co0.05Mn0.05O2 Lithium Metal Batteries.

Current lithium-ion batteries cannot meet the requirement of higher energy density with further large-scale application of electrical vehicles. Lithium metal batteries combined with Ni-rich layered oxides cathode are expected as the one of promising solutions, while the poor electrode and electrolyte interface impedes the commercial development of lithium metal batteries. A new double-salts super concentrated (DSSC) carbonate electrolyte is proposed to improve the electrochemical performance of LiNi0.90Co0.05Mn0.05O2 (NCM9055)||Li metal battery which exhibits stable cycling performance with the capacity retention of 93.04% and reversible capacity of 173.8 mAh g-1 after 100 cycles at 1 C, while cells with conventional 1m diluted electrolyte remains only 60.55% and capacity of 114.2 mAh g-1. The double salts synergistic effect in super concentrated electrolyte promotes the formation for more balanced stable cathode electrolyte interface (CEI) inorganic compounds of CFx, LiNOx, SOF2, Li2SO4, and less LiF by X-ray photoelectron spectroscopy (XPS)test, and the uniform 2-3nm rock-salt phase protection layer on the cathode surface by transmission electron microscope (TEM) characterization, improving the cycling performance of the Ni-rich NCM9055 layered oxide cathode. The DSSC electrolyte also can relief the Li dendrite growth on Li metal anode, as well as exhibit better flame retardance, promoting the application of more safety Ni-rich NCM9055||Li metal batteries.

BDD-persulfate-based anodic oxidation process for progestin degradation: Optimization of conditions, eco-compatibility tests, and cost evaluation

Considering the increasing presence of the hormones levonorgestrel (LNG) and gestodene (GES) in wastewater, the limited effectiveness of conventional treatment methods, and the demand for advanced complementary processes, our study aimed to optimize an anodic oxidation treatment with a focus on low specific energy consumption (SEC) and costs. An electrochemical system coupled to a boron-doped diamond anode (BDD) was continuously used to treat synthetic and real pharmaceutical wastewater from contraceptive production. The central design composite and response surface methodology were the tools employed for optimization. The lowest SEC was obtained as a response to the main process variables: current density, initial pH, and the concentration of the support electrolyte ([Na2S2O8]). The optimal condition ([Na2S2O8]0 = 0.07 mol L−1; [LNG]0,RPW = 1.02±0.05 mg L−1 and [GES]0,RPW = 1.05±0.05 mg L−1; j = 37.5 mA cm−2; pH = 6.75) was established considering an SEC ≤ 3.6 ± 0.8 kWh g−1 and progestins removal ≥70%, which was the experimental condition used to evaluate acute toxicity to Daphnia similis and the effect on estrogenic activity removal using the YES assay. Notably, our study evaluated, for the first time, a comparative investigation that highlights the substantial effect of support electrolytes over the eco-compatibility assessment of the anodic oxidation process investigated. The adaptability of the operation indicates the prospective suitability for the implementation of the process in wastewater treatment facilities in the pharmaceutical industry.

Long-life potassium metal batteries enabled by anion-derived solid electrolyte interphase using concentrated ionic liquid electrolytes

Potassium metal batteries (PMBs) show great potential as next-generation energy storage systems yet face challenges such as the dendritic growth of the potassium anode, leading to issues with cycle life and safety. This study reports a potassium salt-concentrated ionic liquid electrolyte (PCIL) consisting of potassium bis(fluorosulfonyl)imide (KFSI) and 1-methyl-1-propyl pyrrolidinium bis(fluorosulfonyl)imide (Pyr13FSI) to achieve long-life and, safe PMBs. PCIL presents several advantages including outstanding oxidation stability (≈5.2 V), decent ionic conductivity (4.0 mS cm−1 at 25 °C), and negligible flammability. Moreover, PCIL promotes the development of anion-derived solid-electrolyte interphase (SEI) with high inorganic content. This not only hinders the growth of potassium dendrites but also facilitates facile interfacial charge transfer kinetics. Benefiting from these advantages, PMBs (K||KVPO4F) employing PCIL exhibit remarkable cycle performances at both ambient and elevated temperatures (capacity retention after 300 cycles: 74.8% at 25 °C and 82.9% at 45 °C), surpassing the performance of conventional carbonate (1 M KPF6 EC/PC) and dilute potassium ionic liquid electrolyte (PIL). This work demonstrates the tangible capability of PCIL in realizing practical PMBs.

Salt gradient enhanced sensitivity in nanopores for intracellular calcium ion detection

Intracellular calcium ion detection is of great significance for understanding the cell metabolism and signaling pathways. Most of the current ionic sensors either face the size issue or sensitivity limit for the intracellular solution with high background ion concentrations. In this paper, we proposed a calmodulin (CaM) functionalized nanopore for sensitive and selective Ca2+ detection inside living cells. A salt gradient was created when the nanopore sensor filled with a low concentration electrolyte was in contact with a high background concentration solution, which enhanced the surface charge-based detection sensitivity. The nanopore sensor showed a 10 × sensitivity enhancement by application of a 100-fold salt gradient, and a detection limit of sub nM. The sensor had a wide detection range from 1 nM to 1 mM, and allowed for quick calcium ion quantification in a few seconds. The sensor was demonstrated for intracellular Ca2+ detection in A549 cells in response to ionomycin.

How Metal/Insulator Interfaces Enable an Enhancement of the Hydrogen Evolution Reaction Kinetics

AbstractThe nanostructuring of electrodes is a common way of increasing electrocatalytic activity. Yet, the fact that the presence of insulating material in nanostructured composites can have a positive effect on efficiency was an unexpected recent finding. The rate enhancement has been linked to different electric fields at the insulator and metal interfaces, facilitating enhanced transport of reaction products into the bulk electrolyte. In this article, we further uncover the origin of the rate enhancement with parameter studies and simulations. We experimentally investigate various parameter dependencies of the alkaline Hydrogen Evolution Reaction (HER) on well‐defined nanometer‐sized Au arrays embedded in a silicon nitride insulating layer. We find a significant enhancement of the HER for all experimental conditions and opposite activity trends with pH, electrolyte concentration and the cationic species compared to a continuous Au electrode. Using a mean field model, we quantify the electrostatic interfacial pressure above the Au and the insulator patches. Combining the double layer simulations with rate equations, we demonstrate that all parameter variations can be consistently explained by the fact that the double layer structure above the insulator patches is much less rigid than above the metal islands and is independent of the applied potential.

Why Bubbles Coalesce Faster than Droplets: The Effects of Interface Mobility and Surface Charge.

Air bubbles in pure water appear to coalesce much faster compared to oil emulsion droplets at the same water solution conditions. The main factors explaining this difference in coalescence times could be interface mobility and/or pH-dependent surface charge at the water interface. To quantify the relative importance of these effects, we use high-speed imaging to monitor the coalescence of free-rising air bubbles with the water-air interface as well as free-falling fluorocarbon-oil emulsion droplets with a water-oil interface. We measure the coalescence times of such bubbles and droplets over a range of different water pH values (3.0, 5.6, 11.0). In the case of bubbles, a very fast coalescence (milliseconds) is observed for the entire pH range in pure water, consistent with the hydrodynamics of fully mobile interfaces. However, when the water-air interface is immobilized by the deposition of a monolayer of arachidic acid, the coalescence is significantly delayed. Furthermore, the coalescence times increase with increasing pH. In the case of fluorocarbon-oil droplets, the coalescence is always much slower (seconds) and consistent with immobile interface coalescence. The fluorocarbon droplet's coalescence time is also pH-dependent, with a complete stabilization (no coalescence) observed at pH 11. In the high electrolyte concentration, a 0.6 M NaCl water solution, bubbles, and droplets have similar coalescence times, which could be related to the bubble interface immobilization at the late stage of the coalescence process. Numerical simulations are used to evaluate the time scale of mobile and immobile interface film drainage.

New insights into the photoassisted anodic reactions of n-type 4H SiC semiconductors

This study aims to investigate the photoelectrochemical behavior of the n-type 4H-SiC, focusing on aqueous, hydroxide-based electrolytes. Despite its high stability, this wide-bandgap semiconductor material undergoes electrochemical reactions, such as anodic oxidation or etching, under specific conditions. Since electrons are the majority charge carriers in n-type semiconductors, oxidation processes require above-bandgap illumination. Then, the reaction rate is influenced by the number of electron holes available for an oxidation process and the velocity of the transport of hydroxide ions to/from the surface. The goal is to focus on the essential reaction parameters (i.e., potential and electrolyte concentration) to clarify the reaction mechanism in aqueous (alkaline) electrolytes. Methods with controllable hydrodynamic conditions are required to investigate the transport processes in the electrolyte. Even though the rotating disk electrode (RDE) is a commonly used and powerful method, it is not well suited for our purpose. Photoelectrochemical etching of SiC is extraordinary because it involves both mass transfer phenomena and gas evolution but also needs high-intensity illumination from an appropriate light source. Hence, a new concept for an inverted rotating cell was developed and implemented. This setup was used to study the effect of the mass transport of hydroxide ions on the photoelectrochemical behavior of SiC in each potential region at varying rotation speeds. In order to interpret the experimental findings, a distinct electrical network model was formulated for simulating the results, aiding in unraveling the underlying reaction mechanism. Electrochemical measurements were complemented by surface-sensitive analytical techniques. XPS was the method of choice to investigate the composition of the sample surface before and after etching. SEM and AFM allow the characterization of the surface morphology in the initial stages of etching. The totality of this information provides a complete picture of the complex processes in the vicinity of the semiconductor electrode.Graphical abstract

Impact of Condition Variations on Bioelectrochemical System Performance: An Experimental Investigation of Sulfamethoxazole Degradation.

Bioelectrochemical systems (BESs) are an innovative technology for the efficient degradation of antibiotics. Shewanella oneidensis (S. oneidensis) MR-1 plays a pivotal role in degrading sulfamethoxazole (SMX) in BESs. Our study investigated the effect of BES conditions on SMX degradation, focusing on microbial activity. The results revealed that BESs operating with a 0.05 M electrolyte concentration and 2 mA/cm2 current density outperformed electrolysis cells (ECs). Additionally, higher electrolyte concentrations and elevated current density reduced SMX degradation efficiency. The presence of nutrients had minimal effect on the growth of S. oneidensis MR-1 in BESs; it indicates that S. oneidensis MR-1 can degrade SMX without nutrients in a short period of time. We also highlighted the significance of mass transfer between the cathode and anode. Limiting mass transfer at a 10 cm electrode distance enhanced S. oneidensis MR-1 activity and BES performance. In summary, this study reveals the complex interaction of factors affecting the efficiency of BES degradation of antibiotics and provides support for environmental pollution control.

Physicochemical and electrochemical properties of several readily available anthraquinone aqueous electrolytes

Aqueous organic redox flow batteries (AORFBs) have become a research hotspot due to their resource sustainability and high security. In which, water-soluble anthraquinone derivatives are the most widely used anodic active electrolytes, and their molecular structure, concentration and work temperature have a direct influence on their physicochemical properties and electrochemical performance, while data on such studies are scarce. In this paper, three typical and low-cost anthraquinone derivatives, including sodium anthraquinone-2-sulfonate (AQS) containing −SO3−, 1,4-dihydroxy-9,10-anthraquinone (DHAQ) containing –OH and sodium 3,4-dihydroxy-9,10-anthraquinone-2-sulfonic acid (ARS) containing both −SO3− and –OH are systemically studied. The effects of temperature, concentration of active electrolyte and supporting electrolyte on the viscosity, conductivity, surface tension and electrochemical properties of these most promising anthraquinone-based electrolytes are investigated systematically. The results show that the three anthraquinone derivatives show obvious differences in physicochemical properties and electrochemical reaction kinetics, and their sensitivity to temperature and concentration is also different, which provides useful information for the design of anthraquinone-based AORFBs.

Strategies of regulating Zn2+ solvation structures toward advanced aqueous zinc-based batteries

Rechargeable aqueous zinc-based batteries not only pave the way for environmentally friendly and safe energy storage devices but also hold great promise for reducing the manufacturing costs of next-generation batteries, positioning them as the most promising energy storage system to replace lithium-ion batteries. However, the commercial application of aqueous zinc-based batteries (AZBs) is severely constrained by issues such as zinc dendrites, hydrogen evolution reaction (HER), and electrode corrosion. While significant efforts have been devoted to exploring electrode materials and their storage mechanisms in this system in recent years, research on the nature of Zn2+ solvation in electrolytes remains insufficient. Therefore, this review primarily provides a comprehensive and in-depth elucidation of the existing issues such as dendrite formation, hydrogen/oxygen evolution, electrode corrosion and passivation interactions. Additionally, from the perspective of electrolyte optimization, this review emphasizes existing strategies to address Zn2+ solvation, including adjusting electrolyte concentration, incorporating functional additives or co-solvents, utilizing ionic liquids, and developing hydrogel electrolytes, and summarizes approaches and mechanisms for improving their relevant performance. Finally, prospects for electrolyte modification and innovation directions of AZBs are proposed, providing guidance for future AZB studies.

Heteroaggregation kinetics of nanoplastics and soot nanoparticles in aquatic environments

Heteroaggregation between polystyrene nanoplastics (PSNPs) and soot nanoparticles (STNPs) in aquatic environments may affect their fate and transport. This study investigated the effects of particle concentration ratio, electrolytes, pH, and humic acid on their heteroaggregation kinetics. The critical coagulation concentration (CCC) ranked CCCPSNPs > CCCPSNPs-STNPs > CCCSTNPs, indicating that heteroaggregation rates fell between homoaggregation rates. In NaCl solution, as the PSNPs/STNPs ratio decreased from 9/1 to 3/7, heteroaggregation rate decreased and CCCPSNPs-STNPs increased from 200 to 220 mM due to enhanced electrostatic repulsion. Outlier was observed at PSNPs/STNPs= 1/9, where CCCPSNPs-STNPs= 170 mM and homoaggregation of STNPs dominated. However, in CaCl2 solution where calcium bridged with STNPs, heteroaggregation rate increased and CCCPSNPs-STNPs decreased from 26 to 5 mM as the PSNPs/STNPs ratio decreasing from 9/1 to 1/9. In composite water samples, heteroaggregation occurred only at estuarine and marine salinities. Acidic condition promoted heteroaggregation via charge screening. Humic acid retarded or promoted heteroaggregation in NaCl or CaCl2 solutions by steric hindrance or calcium bridging, respectively. Other than van der Waals attraction and electrostatic repulsion, heteroaggregation was affected by steric hindrance, hydrophobic interactions, π − π interactions, and calcium bridging. The results highlight the role of black carbon on colloidal stability of PSNPs in aquatic environments.

Nitrous acid electroreduction on macroporous silver foam

In this paper, silver 3D foams have been synthesized using dynamic hydrogen bubble template and thiocyanate-based deposition bath. The material was used as electrocatalyst for nitrous acid (HNO2) reduction. On this material, we found that overpotential of nitrous acid reduction is decreased by at least 300 mV and the in situ formed nitric oxide (NO) reduction becomes the predominant step when the potential is decreased even further, comparing to flat silver polycrystalline electrode. Another difference between this material and the silver polycrystalline electrode concerns the influence of the nature of supporting electrolyte on the preferred reaction. Precisely, while Ag polycrystalline is preferentially reducing HNO2 into NO in low concentration of perchlorate electrolyte, Ag foam preferentially reduces the in situ formed NO into N2O, in all tested electrolytes, if the same potential range is considered. The initial reduction of HNO2 into NO is better evidenced after the partial removal of thiocyanate species. Finally, the use of isotope 15N in the nitrite salt and of a flow thin layer cell enabled the detection of nitrogen among other gaseous products for both silver foam and flat silver electrode.

Development of a consistent geochemical model of the Mg(OH)2–MgCl2–H2O system from 25°C to 120°C

The formation of magnesium chloride-hydroxide salts (magnesium hydroxychlorides) has implications for many geochemical processes and technical applications. For this reason, a thermodynamic database for evaluating the Mg(OH)2–MgCl2–H2O ternary system from 0 °C–120 °C has been developed based on extensive experimental solubility data. Internally consistent sets of standard thermodynamic parameters (ΔGf°, ΔHf°, S°, and CP) were derived for several solid phases: 3 Mg(OH)2:MgCl2:8H2O, 9 Mg(OH)2:MgCl2:4H2O, 2 Mg(OH)2:MgCl2:4H2O, 2 Mg(OH)2:MgCl2: 2H2O(s), brucite (Mg(OH)2), bischofite (MgCl2:6H2O), and MgCl2:4H2O. First, estimated values for the thermodynamic parameters were derived using a component addition method. These parameters were combined with standard thermodynamic data for Mg2+(aq) consistent with CODATA (Cox et al., 1989) to generate temperature-dependent Gibbs energies for the dissolution reactions of the solid phases. These data, in combination with values for MgOH+(aq) updated to be consistent with Mg2+-CODATA, were used to compute equilibrium constants and incorporated into a Pitzer thermodynamic database for concentrated electrolyte solutions. Phase solubility diagrams were constructed as a function of temperature and magnesium chloride concentration for comparisons with available experimental data. To improve the fits to the experimental data, reaction equilibrium constants for the Mg-bearing mineral phases, the binary Pitzer parameters for the MgOH+ — Cl− interaction, and the temperature-dependent coefficients for those Pitzer parameters were constrained by experimental phase boundaries and to match phase solubilities. These parameter adjustments resulted in an updated set of standard thermodynamic data and associated temperature-dependent functions. The resulting database has direct applications to investigations of magnesia cement formation and leaching, chemical barrier interactions related to disposition of heat-generating nuclear waste, and evaluation of magnesium-rich salt and brine stabilities at elevated temperatures.