Electrolyte Concentration Research Articles

Investigation of the influence of electrolytic milling machining parameters on the machining accuracy of thin-walled parts.

Aircraft parts are often designed as thin-walled structures to reduce the weight of the aircraft. However, thin-walled structures are prone to deformation during the milling process, leading to a decrease in machining accuracy. To address this problem, a method combining milling and electrochemical machining, known as electrolytic milling, is proposed to minimize deformation and enhance the accuracy of thin-walled parts. The factors that affect the machining accuracy of electrolytic milling were analysed, and a model for predicting the thickness of the material removed was established. Electrolytic milling experiments were designed, and the model was solved. Based on the built model, the influences of feed rate, spindle speed, radial cutting depth, voltage and electrolyte concentration on material removal thickness were investigated. Compared with the milling method, the electrolytic milling method can improve the machining accuracy of thin-walled parts. Electrolytic milling experiments were conducted on box-shaped parts to verify the reliability of the proposed method.

Electrochemical Reactions Affected by Electric Double Layer Overlap in Conducting Nanopores.

When a potential is applied to an electrode immersed in an electrolyte solution, ions with opposite charges accumulate around the electrode, forming an electrical double layer (EDL). Unlike flat electrodes, nanoporous electrodes with pore sizes comparable to the EDL thickness experience overlapping EDLs, altering the electrochemically effective surface area. Although previous research has primarily examined the ion charging dynamics and EDL formation in nanoporous electrodes, the impact of EDL overlap on Faraday reactions remains underexplored. In this study, we examined the influence of EDL overlap on electrochemical reactions within nanoporous electrodes using chronoamperometry and DC and AC voltammetry. We used the electrolyte concentration, measurement duration, overpotential, and electrode material as variables to determine the relationship between the extent of EDL overlap and the electrochemical reaction. The electrolyte concentration-dependent electrochemical reaction due to the EDL overlap was more pronounced for electrodes with faster potential changes, shorter measurement times, lower overpotentials, and slower catalytic activity. This is a unique nanoporous electrochemical phenomenon that is not observed on flat electrodes. These findings provide insight into the utilization of nanoporous electrodes in catalytic and sensor applications.

Parameter Analysis of Anion Exchange Membrane Water Electrolysis System by Numerical Simulation

Anion exchange membrane electrolysis, which combines the advantages of both alkaline electrolysis and proton-exchange membrane electrolysis, is a promising technology to reduce the cost of hydrogen production. The present work focused on the study of the electrochemical phenomena of AEM electrolysis and the investigation of the key factors of the AEM hydrogen production system. The numerical model is established according to electrochemical reactions, polarization phenomena, and the power consumption of the balance of plant components of the system. The effects of operation parameters, including the temperature and hydrogen pressure of the electrolyzer, electrolyte concentration, and hydrogen supply pressure on the energy efficiency are studied. The basic electrochemical phenomena of AEM water electrolysis cells are analyzed by simulations of reversible potential and activation, and ohmic and concentration polarizations. The results reveal that increasing the operating temperature and hydrogen production pressure of the AEM electrolyzer has positive effects on the system’s efficiency. By conducting an optimization analysis of the electrolyzer temperature—which uses the heat energy generated by the electrochemical reaction of the electrolyzer to minimize the power consumption of the electrolyte pump and heater—the AEM system with an electrolyzer operating at 328 K and 30 bar can deliver hydrogen of pressure up to 200 bar under an energy efficiency of 56.4%.

Deciphering supramolecular arrangements, micellization patterns, and antimicrobial potential of bacterial rhamnolipids under extreme treatments of temperature and electrolyte

The micellization properties of rhamnolipids (RLs) in extreme electrolyte concentrations and temperatures have gained considerable attention due to their broad industrial applications. In this study, the aggregation behavior, specifically the micellization pattern (critical micelle concentration (CMC)) of RLs produced from a newly isolated thermophilic strain of Pseudomonas aeruginosa from a harsh environment of an oil field, was investigated by a spectrophotometric method at various temperatures (293–393 K) and electrolyte concentrations (NaCl: 2–20%). The result indicated that the CMC values (0.267–0.140 mM⋅dm−3) were both electrolyte- and temperature-dependent exhibiting a U-shaped trend as temperature and NaCl concentration increased. Variations in NaCl concentration and temperature also affected the standard Gibbs free energy (ΔGomic), enthalpy (ΔHomic), and entropy (ΔSomic) of micellization. The molecule also showed stability at a broad range of temperatures, pH, and NaCl concentrations. Thin-layer chromatography (TLC) and Fourier-transform infrared (FTIR) analysis confirmed the similarity in composition between the crude extract and the commercial RL with Rf values of 0.72 for mono-rhamnolipids and 0.28 for di-rhamnolipids. FTIR analysis confirmed the chemical nature particularly key aliphatic functional groups present in the fatty acid tail of RLs and the -COC- bond in the structure of the rhamnose moiety. Additionally, LC-ESI-QTOF analysis confirmed corresponding ionic fragments of mono- and di-rhamnolipids congeners. Furthermore, the antimicrobial potential was determined against different human pathogens in the absence and presence of NaCl by measuring zones of inhibition. The result revealed enhanced inhibitory effects against Gram-positive pathogens (S. aureus, S. epidermidis, and L. monocytogene), with zones of inhibition of 26, 30, and 20 mm in the presence of NaCl. These findings underline the role of NaCl in the micellization of RL molecules and highlight their importance in environmental applications, pharmaceuticals, and various life science sectors.

The Donnan equilibrium is still valid in high-volume HDF.

Clinical studies have shown that hemodiafiltration reduces morbidity and mortality of dialysis patients compared to hemodialysis alone. This is attributed to its superior middle molecule clearance compared to standard hemodialysis. However, doubts arose as to whether a high convective flux through the dialyzer membrane has an influence on the equilibrium concentration of small ions, especially that of sodium. Due to the presence of negatively charged impermeable proteins on the blood side, the Gibbs-Donnan effect leads to an asymmetric distribution of membrane permeable ions on both sides of the membrane. In thermodynamic equilibrium, the concentrations of those ions can easily be calculated. However, the convective fluid flow leads to deviations from thermodynamic equilibrium. In this article, the effect of a convective flow on the ion distribution across a semipermeable membrane is analyzed in a theoretical model. Starting from the extended Nernst-Planck equation, including diffusive, convective, and electrostatic effects, a set of differential equations is derived. An approximate solution for flow speeds up to 0.1 ms-1 as well as a numerical solution are given. The results show that in any practical dialysis setting the convective flow has negligible influence on the electrolyte concentrations.

Nonlinear conductivity of aqueous electrolytes: Beyond the first Wien effect.

The conductivity of strong electrolytes increases under high electric fields, a nonlinear response known as the first Wien effect. Here, using molecular dynamics simulations, we show that this increase is almost suppressed in moderately concentrated aqueous electrolytes due to the alignment of the water molecules by the electric field. As a consequence of this alignment, the permittivity of water decreases and becomes anisotropic, an effect that can be measured in simulations and reproduced by a model of water molecules as dipoles. We incorporate the resulting anisotropic interactions between the ions into a stochastic density field theory and calculate ionic correlations as well as corrections to the Nernst-Einstein conductivity, which are in qualitative agreement with the numerical simulations.

Serum electrolyte abnormalities in cats with chronic inflammatory enteropathy.

Limited information is available on electrolyte abnormalities in cats with chronic inflammatory enteropathy (CIE). Report the prevalence of electrolyte abnormalities in cats with CIE compared to other gastrointestinal disorders, and determine their association with disease and outcome variables in cats with CIE. Three hundred twenty-eight client-owned cats from 2 referral hospitals: CIE (132), alimentary small cell lymphoma (29), acute gastroenteritis (48), and healthy controls (119). Retrospective study comparing serum electrolyte concentrations at time of diagnosis among the 4 groups of cats, and associations with clinical signs, intestinal mucosal fibrosis scores, treatment subclassification and outcome in CIE. Cats with CIE had lower sodium and higher potassium concentrations and lower sodium: potassium ratios compared with healthy cats (P < .001, P = .01, and P < .001, respectively). Cats with CIE and a duodenal mucosal fibrosis score of 2 had lower sodium and lower total calcium concentrations compared with cats that had a score of 0 (P = .02 and P = .01). Cats with CIE and a colonic mucosal fibrosis score of 1 had higher potassium concentrations and lower sodium: potassium ratios compared with cats that had a score of 0 (P = .03 and P = .01). Cats with CIE that died as a result of their disease had higher potassium concentrations and lower sodium: potassium ratios compared to cats that were alive (P = .02 and P = .01). Electrolyte abnormalities occur with CIE and, in particular, in cats with higher fibrosis scores and worse outcomes. Further research should aim to determine the pathogenesis of these findings and identify novel therapeutic targets for cats with CIE.

Reducing Dead Species by Electrochemically-Densified Cathode-Interface-Reaction Layer towards High-Rate-Endurable Zn||I-Br Batteries.

Interhalogen-involved aqueous Zn||halogen batteries (AZHBs) are latent high-energy systems for grid-level energy storage, yet usually suffer from poor high-rate endurability caused by the formation of "dead species". Herein, via an electrochemically-densified cathode-interface-reaction layer (CIRL), Zn||I-Br batteries involving interhalogen reactions between the I2 cathode and Br- from the electrolytes are initially achieved with excellent high-rate endurability. Different from that in diluted electrolytes, the CIRL formed in Br--concentrated electrolyte is denser and water-lean, which enables halogen species conversion with a more rapid charge transfer and lower activation energy. More importantly, the CIRL robustly affords a decent I2 conservation by accelerated conversion kinetics and limited species diffusion, thereby endowing the Zn||I-Br batteries with an ultralong high-rate lifespan. The electrochemical mechanism is sufficiently verified by multiple spectral characterizations. Consequently, Zn||I-Br batteries in Br--concentrated (20 m) electrolytes exhibit an overwhelming rate capability and lifespan to those in Br--diluted (2 m) electrolytes. Typically, when cycled at a large current density of 10 A g-1, an ultralong lifespan of over 25,000 cycles is achieved with a high retention of 98.3%. This study provides new insight into the CIRL-dictated active species conservation for high-rate endurable AZHBs, which could apply to other high-energy interhalogen batteries.

Modified Debye-Hückel-Onsager theory for electrical conductivity in aqueous electrolyte solutions: Account of ionic charge nonlocality.

This paper presents a mean field theory of electrolyte solutions, extending the classical Debye-Hückel-Onsager theory to provide a detailed description of the electrical conductivity in strong electrolyte solutions. The theory systematically incorporates the effects of ion specificity, such as steric interactions, hydration of ions, and their spatial charge distributions, into the mean-field framework. This allows for the calculation of ion mobility and electrical conductivity, while accounting for relaxation and hydrodynamic phenomena. At low concentrations, the model reproduces the well-known Kohlrausch's limiting law. Using the exponential (Slater-type) charge distribution function for solvated ions, we demonstrate that experimental data on the electrical conductivity of aqueous 1:1, 2:1, and 3:1 electrolyte solutions can be approximated over a broad concentration range by adjusting a single free parameter representing the spatial scale of the nonlocal ion charge distribution. Using the fitted value of this parameter at 298.15K, we obtain good agreement with the available experimental data when calculating electrical conductivity across different temperatures. We also analyze the effects of temperature and electrolyte concentration on the relaxation and electrophoretic contributions to total electrical conductivity, explaining the underlying physical mechanisms responsible for the observed behavior.

Electrochemical dissolution of titanium under alternating current polarization to obtain its dioxide

Abstract The titanium electrode was polarized under the influence of alternating current (AC) at 50 Hz. The current density was varied between 100 and 5,000 A m−2. Initially, the titanium electrode oxidized, and then, titanium oxides were reduced during the cathodic half-cycle of the AC. When the cathodic half-cycle changes to the anodic half-cycle, titanium is oxidized to the trivalent state: Ti − 3 e ̄ → Ti 3 + {{\rm{Ti}}-3{\rm{e}}{\rm{&amp;#x0304;}}\to {\rm{Ti}}}^{3+} . The direction of the AC changes depending on its frequency, causing the processes occurring on the electrodes to be periodically repeated. The current efficiency of the titanium electrode dissolution depends on the sulfuric acid concentration and electrolyte concentration, reaching up to 63.4% under optimal conditions. Bipolar electrodes were used during AC electrolysis. It was found that the decrease in the mass of titanium electrodes increases almost linearly at first, from 400 to 1,600 A m−2, and then more intensively within the current densities from 1,800 to 2,500 A m−2. It was shown that when using a bipolar electrode, the total mass loss of the electrodes is 1.38 times greater than the total mass loss during polarization without a bipolar electrode. The composition of the titanium dioxide obtained as a result of electrolysis was identified using physico-chemical analysis methods.

Importance of Electrolytes in Exercise Performance and Assessment Methodology After Heat Training: A Narrative Review

Performing exercise in hot environmental conditions presents athletes with potential negative physiological and perceptual implications. Key constituents, such as fluid and electrolytes, are lost during sweating through the process of cooling the human body. The loss of electrolytes impairs exercise performance. Heat training is one strategy to combat sweat electrolyte loss, with decreased sweat electrolyte concentration being a main sudomotor adaptation. To measure sweat electrolyte concentration, two common assessment methods are typically utilized: whole-body washdown and regional sweat patch measurements. The effects of physiological adaptations and sweat electrolyte assessment methodology have been investigated; however, the importance of methodological differences between sweat electrolyte measurements following heat training has yet to be explored. This review explores the differences between sweat electrolyte measurement techniques following adaptations incurred with heat training. Future research directions are also provided.

Anodic Dissolution Behavior of DD6 Nickel-Based Single Crystal Superalloy for Electrochemical Machining Applications

Abstract Nickel-based single crystal superalloys have been widely used in turbomachinery components. Electrochemical machining (ECM) is an essential method for shaping such high-performance alloys. Understanding the fundamentals of ECM for these alloys is crucial for the design and optimization of the process. This study investigated the anodic dissolution of DD6 nickel-based single crystal superalloy in concentrated NaCl and NaNO3 electrolytes under ECM conditions. Polarization curves showed a passive-transpassive transition behavior in both electrolytes. Galvanostatic experiments demonstrated unique current efficiency characteristics contradicting the empirical ECM knowledge. Surface analyses revealed that the anomalous current efficiency of &gt;100% in the NaNO3 electrolyte results from the falling of γ’ phases from anodic surfaces due to the preferential dissolution of the γ matrix phase. The transition from selective to uniform dissolution with increased current density and reduced electrolyte flow velocity leads to decreased current efficiency in NaNO3 electrolyte. The removal of both γ and γ’ phases depends entirely on electrochemical dissolution in NaCl electrolyte, ensuring that current efficiency maintains a normal value. A schematical anodic interface model was proposed to describe the dissolution behavior.

First‐Principles Molecular Dynamics Study on Reductive Stability of High Concentration Electrolyte on Zn Doped Cu Current Collector Surface

AbstractIn enhancing the lifespan of anode‐free Li metal batteries (AFLMBs), current collector (CC) engineering is crucial for achieving uniform and dendrite‐free lithium deposition. The commonly used copper (Cu) CC is unsatisfactory because of its poor lithiophilicity. Here, we consider Zn doping on the Cu CC surface (Zn−Cu) and explore the reductive stability of a high‐concentration electrolyte (HCE), consisting of 3.6 M Lithium Hexafluorophosphate (LiPF6) salt in a mixture of ethylene carbonate (EC) and diethylcarbonate (DEC), on the Zn−Cu (111) surface (HCE|Zn−Cu) using density functional theory (DFT) and ab initio molecular dynamics (AIMD) simulations. The interfacial reactions in the HCE|Zn−Cu system are compared to those on the pristine Cu (111) surface (HCE|Cu). We have also studied the effect of electron‐rich environments on the decomposition mechanism of the HCE mixture on both the CC surfaces. It is found that the HCE mixture is electrochemically stable on both Cu and Zn−Cu surfaces in a neutral environment. However, under electron‐rich conditions, only one DEC molecule has decomposed upon contact with the Cu CC surface, while the two PF6− anion groups from Li salts have decomposed much faster (within 100 fs) when the HCE mixture interacts with the Zn−Cu surface. Our results indicate that Zn doping suppresses undesirable solvent decomposition and improves the quality of the solid electrolyte interphase (SEI) layer.

Unveiling graphite anodic expansion: Insights from electrochemical techniques, mass spectrometry, and kinetic modelling

Anodic expansion of graphite at different pH has been studied by coupling a mass spectrometer to an electrochemical cell. The mass spectrometry technique permits to follow the electrochemical gasification of graphite as well as the reaction products formed from the electrolyte. The current and mass spectrometry signals suggest that the neutral medium is the least aggressive for expansion. In addition, chronoamperometric expansion of graphite at different potentials has been carried out using the neutral medium. This experimental approach permits to get detailed information about the reaction mechanism that produces graphene-oxide based materials. The effect of potential and electrolyte concentration have been studied, and it has been observed that the degree of oxidation of the graphene oxide material obtained can be controlled. In addition, a kinetic model based on a phase-moving boundary has been used to describe the chronoamperometric experiments. Two types of graphene oxide materials have been obtained with the anodic synthesis and have been classified as few-layer graphene oxide (FLGO) and graphene oxide quantum dots (GOQDs). The physicochemical and electrochemical properties of both products have been studied.

Quantitative Analysis of Complex Aluminum Electrolytes by X-Ray Fluorescence.

The future production of electrolytic aluminum will be characterized by low temperature, low carbon emissions, and environmental friendliness, which will result in a more complex electrolyte system. Real-time analysis of electrolytes can significantly enhance the efficiency of the electrolytic process. However, accurately analyzing the composition of complex aluminum electrolytes online has been a technical challenge. This research primarily focuses on determining the ingredient contents of complex aluminum electrolytes based on elemental concentrations measured using X-ray fluorescence (XRF) according to an applicable standard. Calibration curves were established based on 53 standard samples of complex aluminum electrolytes to establish relationships between XRF fluorescence intensity and real concentrations. Analysis conducted on industrial complex electrolytes confirms that these newly constructed curves effectively reduce relative errors to less than 3%. Additionally, a feasible solution is proposed for determining the cryolite ratio (CR) in aluminum electrolytes using XRF. Results demonstrate an average deviation as low as approximately 0.02, fully meeting industrial production requirements. This technique offers numerous benefits including rapid analysis, ease of use, and cost savings.

Study on the electrochemical oxidation mechanism of sulfamethoxazole using three-dimensional boron-doped diamond

In this study, we prepared a novel three-dimensional boron-doped diamond (BDD) electrode. Subsequently, we systematically conducted an electrochemical oxidation reaction on sulfamethoxazole (SMX) using a BDD anode and a platinum plate (Pt) cathode. The effects of initial concentration, current density, initial pH, and carrier electrolyte on SMX degradation were investigated. The SMX was completely removed after 4 h of electrolysis at a current density of 30 mA/cm2, 0.1 mol sodium sulphate as the supporting electrolyte, and a pH of 7. Additionally, the COD removal rate was 65.6 %, while the energy consumption was 40.1 %. Compared with two-dimensional BDD electrode degradation, the energy saving was 54 %. Density functional theory (DFT) and high-performance liquid chromatography (HPLC) were used to analyse the SMX degradation mechanism. Three possible degradation pathways were proposed: ·OH substitution of the amino group in the aromatic ring, oxidation of the amino group to nitrogen dioxide, and addition of ·OH to the isoxazole ring. The active sites detected in the reaction corresponded closely with the calculated results using DFT. Moreover, ECOSAR toxicity analysis was applied to evaluate the toxicity of the intermediates produced during electrolysis. We discovered that the toxicity of SMX and its intermediates decreased significantly during electrolysis.

Study on solubility and solvation thermodynamics for the advancement of biorelevant activities of l-isoleucine and l-serine in aqueous ammonium chloride solutions in the temperature range of 288.15–308.15 K

This study investigated the dissolution behavior of l-isoleucine and l-serine in an aqueous salt solution (ammonium chloride), examining how variations in temperature and electrolyte concentration affect their solubility. We conducted careful experiments and used mathematical calculations to explore interactions at a molecular level. We observed that the structure of these amino acids and salt concentration in the aqueous medium influence their interactions, which affects dissolution. In the presence of electrolytes, l-isoleucine demonstrated a salting-out effect whereas l-serine showed a salting-in effect. This work examines the solute–solvent interactions of these solutes in aqueous ammonium chloride solutions. l-isoleucine exhibits a nonspontaneous reaction with increasing salt concentrations whereas l-serine shows spontaneous behavior. Gibbs free energy analysis revealed greater stability of l-serine. The pH and conductance measurements showed how these factors influence solution properties. This insight helps us comprehend the nature and behavior of these molecules in different situations, which could be helpful in drug formulation or protein purification in the future.

Photoaging-induced variations in heteroaggregation of nanoplastics and suspended sediments in aquatic environments: a case study on nanopolystyrene

Photoaging of nanoplastics (NPs) and heteroaggregate with suspended sediments (SS) determines transport processes and ecological risks of NPs in aquatic environments. This study investigated the disruption of photoaging on the heteroaggregation behavior of polystyrene NPs (PSNPs) and SS in different valence electrolyte solutions and deduced the interaction mechanisms by integrating aggregation kinetics and molecular dynamics (MD) simulation. Increasing the electrolyte concentration significantly enhanced the heteroaggregation between PSNPs and SS, and the divalent electrolytes induced the heteroaggregation more efficiently. MD simulation at the molecular level revealed that PS and SS could spontaneously form clusters, and photoaged PS has a stronger potential to fold into a dense state with SS. Photoaging for 30 d retarded heteroaggregation due to the steric hindrance produced by the leached organic matter in NaCl solutions, and the critical coagulation concentration (CCC) increased by more than 85.44%. Contrarily, photoaging caused more oxygen-containing functional groups produced on the surface of PSNPs through Ca2+ bridging promoting heteroaggregation and thus destabilizing in CaCl2 solutions, the CCC decreased by 23.53% ∼ 35.29%. These findings provide mechanistic insight into the environmental process of NPs and SS and are crucial for a comprehensive understanding of the environmental fate and transport of NPs in aquatic environments.

Investigation of Structural and Thermal Properties of Mg(ClO4)2 Based PVC + ZnO Nanocomposite Polymer Electrolytes

PVC+ZnO+Mg(ClO4)2 nanocompistie polymer electrolyte of differnet concentrations of Mg(ClO4)2 electrolytes were prepared using solution casting technique and further characterized using XRD, FTIR and TGA &amp; DTA. The results of XRD suggests that the high amorphous of the PVC/ZnO nanocomposite with x=50 wt.% Mg(ClO4)2. As it due to high amorphous nature it can show a good ionic conductivity. The FTIR peaks shifting may also representing change of bond length and attaining good amorphous nature. The high heat resistance for all the sample can notice for DGA-DTA. Key word: polymer electrolyte, XRD, FTIR, TGA &amp; DTA, Nanofiller

Tailoring CO2 detection capabilities using Co-ZnO/MoS2 nanocomposites through electrolyte concentration modulation

The current study explores a new approach to investigate the CO2 detection capabilities of cobalt-doped zinc oxide (Co-ZnO) combined with molybdenum sulfide (MoS2) hybrid nanomaterials Co-ZnO/MoS2 (CZM). The hydrothermally synthesized CZM composites provide unique structural and compositional properties, with 25 nm as their longest dimension (length), and specific lattice structure. CZM-based electrodes are developed by preparing the nanomaterial-dispersed ink, and potentiometric studies explore the optimal sensing performance. We found significant enhancements in sensitivity, reaction time, and reduction efficiency by systematically changing the electrolyte concentration in the electrode cell. Bode and Nyquist plots explain the influence of electrolyte concentration and the nanomaterial synergy in CO2 sensing and conversion with the 0.1 N electrolyte with the maximum efficiency. By offering important insights into how the electrolyte content affects the performance of Co-ZnO/MoS2 nanocomposite sensors, this study advances the field of CO2 sensing technology. Further, the nanomaterials extend their applicability in environmental monitoring, evaluating indoor air quality, and industrial processes.