Ion Concentration Research Articles

Effect of the global electroneutrality condition on electromigration Taylor-Aris dispersion in a microcapillary with finite Debye layer thickness.

In this work, the electromigration dispersion (EMD) due to the charged electrolytes in microchannels is considered without using the thin electrical double layer assumption. The electrokinetic flow and transport of ions are actuated within a rectangular micro-/nanochannel having a negative surface charge density under the influence of an external electric field. Due to the local variation of the conductivity and the nonvalidity of the electroneutrality condition, the local electric field varies as a function of the solute concentration, wall surface charge density, valency, and Debye layer length. The resulting electrokinetic flow due to the external electric field drives the fluid along with the charged species, where the Taylor-Aris dispersion separates the solutes into their different constituents. The local concentration dependence of the electric field leads to the formation of concentration profiles that are slightly asymmetric with respect to the standard Gaussian distribution. Including a finite Debye layer thickness has an effect on the advection of the species as well as the diffusion of the species. It is found that in cases where Debye layers are thicker, the species advects faster within the microchannel. This might give valuable insights into the nature of the EMD. Our model aims to predict the evolution of ionic concentration at all positions within the channel. A study of the higher-order statistics in skewness and kurtosis has also been conducted to obtain a better understanding of the idealized model consisting of a buffer solution.

Evaluation of total, soluble and ionic fluoride concentration in whitening and desensitizing toothpastes.

Due to the popularity and increasing launch of toothpastes with whitening and sensitivity properties on the market, this study aimed to evaluate the fluoride concentrations in these products, since the concentrations of fluoride directly interfere with the anti-caries potential. This is an experimental, invitro study, where 37 samples from different batches (n = 3) purchased in different countries, were analysed in duplicate, via the ion-selective electrode technique to verify the concentration (μg/g or ppm F-) of total fluoride (TF), total soluble fluoride (TSF) and ionic fluoride (IF). For a comparative data analysis, ANOVA was applied followed by a Tukey's test for multiple comparisons. The level of confidence adopted was 95%. In the 37 assessed toothpastes, 45.9% contained NaF and 54.1% sodium monofluorophosphate (MFP). The TF found in the formulations ranged from 902.8 to 1539.4 ppm of F (mean: 1165.2 ± 179.3); fluoride concentration in the TSF fraction ranged from 708.8 to 1306.7 ppm of F (mean: 959.5 ± 162.4); IF results ranged from 101.9 to 1162.3 ppm of F (642.2 ± 294.1). Significant differences (p < 0.05) were found in the concentrations of the 59.5% assessed toothpastes in comparisons between declared and measured total fluoride (TF) concentrations, as well as in 62.2% when total fluoride (TF) and total soluble fluoride (TSF) were compared. In this study, most of the samples evaluated showed discrepancies when compared to the information declared by the manufacturers. In addition, the soluble concentrations found in half of the samples were lower than total concentrations and this may affect anti-caries effectiveness.

A Zero-Voltage-Writing Artificial Nervous System Based on Biosensor Integrated on Ferroelectric Tunnel Junction.

The artificial nervous system proves the great potential for the emulation of complex neural signal transduction. However, a more bionic system design for bio-signal transduction still lags behind that of physical signals, and relies on additional external sources. Here, we present a zero-voltage-writing artificial nervous system (ZANS) that integrates a bio-source-sensing device (BSSD) for ion-based sensing and power generation with a hafnium-zirconium oxide-ferroelectric tunnel junction (HZO-FTJ) for the continuously adjustable resistance state. The BSSD can use ion bio-source as both perception and energy source, and then output voltage signals varied with the change of ion concentrations to the HZO-FTJ, which completes the zero-voltage-writing neuromorphic bio-signal modulation. In view of in-/ex-vivo biocompatibility, we show the precise muscle control of a rabbit leg by integrating the ZANS with a flexible nerve stimulation electrode. The independence on external source enhances the application potential of ZANS in robotics and prosthetics. This article is protected by copyright. All rights reserved.

Exogenous zinc application mitigates negative effects of salinity on barley (Hordeum vulgare) growth by improving root ionic homeostasis.

Detrimental effects of salinity could be mitigated by exogenous zinc (Zn) application; however, the mechanisms underlying this amelioration are poorly understood. This study demonstrated the interaction between Zn and salinity by measuring plant biomass, photosynthetic performance, ion concentrations, ROS accumulation, antioxidant activity and electrophysiological parameters in barley (Hordeum vulgare L.). Salinity stress (200mM NaCl for 3weeks) resulted in a massive reduction in plant biomass; however, both fresh and dry weight of shoots were increased by ~30% with adequate Zn supply. Zinc supplementation also maintained K+ and Na+ homeostasis and prevented H2 O2 toxicity under salinity stress. Furthermore, exposure to 10mM H2 O2 resulted in massive K+ efflux from root epidermal cells in both the elongation and mature root zones, and pre-treating roots with Zn reduced ROS-induced K+ efflux from the roots by 3-4-fold. Similar results were observed for Ca2+ . The observed effects may be causally related to more efficient regulation of cation-permeable non-selective channels involved in the transport and sequestration of Na+ , K+ and Ca2+ in various cellular compartments and tissues. This study provides valuable insights into Zn protective functions in plants and encourages the use of Zn fertilisers in barley crops grown on salt-affected soils.

Sequestration of cyanide ions from aqueous medium by physio-chemically fabricated biochar of peels of banana and grape fruit in ecofriendly way.

Pakistan is an agricultural country producing plenty of fruits, like: mango, banana, apple, peaches, grapes, plums, variety of citrus fruits including lemon, grapefruit, and oranges. So far the peels of most of the fruits are usually wasted and not properly utilized anywhere. In this work, the peels of banana and grapefruit are converted into biochar by slow pyrolysis under controlled supply of air and used for sequestering cyanide ions from aqueous medium after chemical modification with ZnCl2 and sodium dodecyl sulfate (SDS). The modified biochar was characterized by various instrumental techniques, like: SEM, FTIR, TGA, and CHNS. Different parameters, like: time, temperature, pH, and dose of adsorbent affecting the adsorption of cyanide ions, onto prepared biochar were optimized and to understand the adsorption phenomenon, kinetic and thermodynamic studies were performed. Concentration of cyanide ions was estimated by employing standard ion selective electrode system and it is found that Sodium Dodecyl Sulfate treated biochar of banana peels shown more adsorption capacity, i.e.,: 17.080 mg/g as compared to all samples. Present work revealed that the biochar produced from the fruit waste has sufficient potential to eliminate trace quantities of cyanide from water, especially after treatment with sodium dodecyl sulfate.

Ionic reverberation modulates the cellular fate of CD8+ tissue resident memory T cells (TRMs) in patients with renal cell carcinoma: A novel mechanism.

In metastatic renal cell carcinoma (mRCC), existing treatments including checkpoint inhibitors are failed to cure and/or prevent recurrence of the disease. Therefore, in-depth understanding of tumor tissue resident memory T cells (TRMs) dysfunction are necessitated to enrich efficacy of immunotherapies and increasing disease free survival in treated patients. In patients, we observed dysregulation of K+, Ca2+, Na2+ and Zn2+ ion channels leads to excess infiltration of their respective ions in tumor TRMs, thus ionic gradients are disturbed and cells became hyperpolarized. Moreover, overloaded intramitochondrial calcium caused mitochondrial depolarization and trigger apoptosis of tumor TRMs. Decreased prevalence of activated tumor TRMs reflected our observations. Furthermore, disruptions in ionic concentrations impaired the functional activities and/or suppressed anti-tumor action of circulating and tumor TRMs in RCC. Collectively, these findings revealed novel mechanism behind dysfunctionality of tumor TRMs. Implicating enrichment of activated TRMs within tumor would be beneficial for better management of RCC patients.

The effects of bathymetry on the long-term carbon cycle and CCD

The shape of the ocean floor (bathymetry) and the overlaying sediments provide the largest carbon sink throughout Earth's history, supporting ~one to two orders of magnitude more carbon storage than the oceans and atmosphere combined. While accumulation and erosion of these sediments are bathymetry dependent (e.g., due to pressure, temperature, salinity, ion concentration, and available productivity), no systemic study has quantified how global and basin scale bathymetry, controlled by the evolution of tectonics and mantle convection, affects the long-term carbon cycle. We reconstruct bathymetry spanning the last 80 Myr to describe steady-state changes in ocean chemistry within the Earth system model LOSCAR. We find that both bathymetry reconstructions and representative synthetic tests show that ocean alkalinity, calcite saturation state, and the carbonate compensation depth (CCD) are strongly dependent on changes in shallow bathymetry (ocean floor ≤600 m) and on the distribution of the deep marine regions (>1,000 m). Limiting Cenozoic evolution to bathymetry alone leads to predicted CCD variations spanning 500 m, 33 to 50% of the total observed variations in the paleoproxy records. Our results suggest that neglecting bathymetric changes leads to significant misattribution to uncertain carbon cycle parameters (e.g., atmospheric CO2 and water column temperature) and processes (e.g., biological pump efficiency and silicate-carbonate riverine flux). To illustrate this point, we use our updated bathymetry for an Early Paleogene C cycle case study. We obtain carbonate riverine flux estimates that suggest a reversal of the weathering trend with respect to present-day, contrasting with previous studies, but consistent with proxy records and tectonic reconstructions.

Efficient operation of atomic frequency comb optical memory using an optical frequency comb in 167Er3+:Y2SiO5

We demonstrated a highly efficient optical memory operation using an atomic frequency comb (AFC) created from a spectrally flattened optical frequency comb with an isotopically pure 167Er3+:Y2SiO5 crystal under zero magnetic field. Compared with standard AFC creation methods such as pulse train method, our method, called comb transfer method, can create a broadband and high-efficiency AFC at lower power and with less effort. This technique can make a significant improvement in the quality of AFCs in crystals doped with low concentrations of rare-earth ions.

Diversifying Ion-Transport Pathways of Composite Solid Electrolytes for High-Performance Solid-State Lithium-Metal Batteries.

The application of composite solid electrolytes (CSEs) in solid-state lithium-metal batteries is limited by the unsatisfactory ionic conductivity underpinned by the low concentration of free lithium ions. Herein, we propose an interface design strategy where an amine silane linker is employed as a coupling agent to graft the Li7La3Zr2O12 (LLZO) ceramic nanofibers to the poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) polymer matrix to enhance their interaction. The hydrogen bonding between amino-functionalized LLZO (NH2@LLZO) and PVDF-HFP not only effectively induces a uniform incorporation of high-content nanofibers (50 wt %) into the polymer matrix but also furnishes sufficient continuous surfaces to weaken the complexation between PVDF-HFP and Li-ion carriers. Additionally, introduction of the hydrogen bond and Lewis acid-base interplay strengthens the interfacial interactions between NH2@LLZO and lithium salts that release more free lithium ions for efficient interfacial transport. The impact of the linker's structure on the dissociation capacity of lithium salts is systematically studied from the steric effect perspective, which affords insights into interface design. Conclusively, the composite solid electrolyte achieves a high ionic conductivity (5.8 × 10-4 S cm-1) by synergy of multiple transport channels at ceramic, polymer, and their interface, which effectively regulates the lithium deposition behavior in symmetric cells. The excellent compatibility of the electrolyte with both LiFePO4 and LiNi0.8Co0.1Mn0.1O2 cathodes also results in a long lifetime and a high rate capability for full cells.

Enhancing ionic conductivity and controlling lithium dendrite growth via ferroelectric ceramic Bi4Ti3O12

BackgroundSolid polymer electrolytes (SPEs) have gained numerous research interest in the field of lithium metal batteries. Solid polymer electrolytes have improved safety compared to liquid electrolytes. Despite this, their low ionic conductivity remains a major barrier to practical applications. To overcome the challenge of low ionic conductivity in SPEs, our study introduces a novel approach that integrates ferroelectric ceramics with polymer solid electrolytes. MethodsWe used a one-step molten salt method to synthesize Bi4Ti3O12 (BIT), combined with a poly (vinylidene difluoride) matrix to form the composite solid-state electrolyte. Through various electrochemical characterizations and COMSOL Multiphysics simulations, we discovered that the ferroelectric properties of BIT significantly increase the dissociation of lithium salts, leading to a greater concentration of mobile lithium ions and more efficient ion transport. Significant findingsThis electrolyte showed a remarkable improvement in lithium-ion conductivity, reaching a value of 8.5 × 10−4 S cm−1 at room temperature. Batteries made with these composite electrolytes demonstrate superior cycling stability, the capacity retention rates for LFP/SPEs/Li cells remain high, reaching 95 % even after 1,000 cycles at room temperature (25 °C). These findings highlight the promising applications of ferroelectric ceramics in solid-state batteries.

Electrochemical ocean iron fertilization and alkalinity enhancement approach toward CO2 sequestration

Achieving net-zero emissions by 2050 requires the development of effective negative emission techniques, including ocean-based approaches for CO2 sequestration. However, the implementation and testing of marine CO2 removal (mCDR) techniques such as ocean iron fertilization (OIF) or ocean alkalinity enhancement (OAE) face significant challenges. Herein, a novel self-operating electrochemical technology is presented that not only combines OIF and OAE, but also recovers hydrogen gas (H2) from seawater, hence offering a promising solution for achieving quantifiable and transparent large-scale mCDR. Experimental results show that the electrochemical OIF (EOIF) can not only increase the concentration of ferrous iron (Fe+2) by 0–0.5 mg/L, but also significantly increases the seawater pH by 8% (i.e., a 25% decrease in the hydrogen ions concentration). The release of iron (Fe+2/Fe+3) can be regulated by adjusting the magnitude of the electric current and its form (e.g., pulsed current and polarity reversal), as well as by optimizing the electrode material and geometry. In certain ocean regions, enhanced iron concentrations stimulate the naturally occurring biological carbon pump (BCP), leading to increased phytoplankton growth, CO2 uptake, and subsequent export of carbon to the deep ocean. Simultaneously, the system increases seawater alkalinity and the buffer capacity, enhancing CO2 solubility and storage in the shallow ocean through the solubility pump. The obtained measurements demonstrate the scalability of EOIF and its ability to operate using solar energy at a lower cost. Overall, the proposed EOIF technology offers a practical, effective, and sustainable solution for addressing climate change on a large scale.

Hypoxia inhibits ferritinophagy-mediated ferroptosis in esophageal squamous cell carcinoma via the USP2-NCOA4 axis.

Esophageal squamous cell carcinoma (ESCC) is a prevalent malignancy of the digestive system. Hypoxia is a crucial player in tumor ferroptosis resistance. However, the molecular mechanism of hypoxia-mediated ferroptosis resistance in ESCC remains unclear. Here, USP2 expression was decreased in ESCC cell lines subjected to hypoxia treatment and was lowly expressed in clinical ESCC specimens. Ubiquitin-specific protease 2 (USP2) depletion facilitated cell growth, which was blocked in USP2-overexpressing cells. Moreover, USP2 silencing enhanced the iron ion concentration and lipid peroxidation accumulation as well as suppressed ferroptosis, while upregulating USP2 promoted ferroptotic cell death in ESCC cells. Furthermore, knockout of USP2 in ESCC models discloses the essential role of USP2 in promoting ESCC tumorigenesis and inhibiting ferroptosis. In contrast, overexpression of USP2 contributes to antitumor effect and ferroptosis events in vivo. Specifically, USP2 stably bound to and suppressed the degradation of nuclear receptor coactivator 4 (NCOA4) by eliminating the Lys48-linked chain, which in turn triggered ferritinophagy and ferroptosis in ESCC cells. Our findings suggest that USP2 plays a crucial role in iron metabolism and ferroptosis and that the USP2/NCOA4 axis is a promising therapeutic target for the management of ESCC.

Spectral studies of thermally stable Dy3+/Sm3+ co-doped Li2Ba5W3O15 phosphors for warm white LEDs

In the current study, a series of Li2Ba5W3O15: RE3+ (RE = Dy, Sm) [LBW:Dy3+/Sm3+] phosphors were prepared using a high-temperature solid-state method. X-ray diffraction, Scanning electron microscopy with energy-dispersive x-ray analysis scans showed that the crystal form was consistent with the standard LBW and comprised small irregularly shaped particles. Diffuse reflectance spectral (DRS) data was utilized to calculate the band gaps. Fluorescence study shows that LBW material doped with Dy3+ and Sm3+ yield distinct colors at 496 nm (blue) for Dy3+ and 582 nm (green-yellow), 612 nm (yellow), and 669 nm (red) for Sm3+ when excited by near-ultraviolet (336 nm) light. The observation of energy transfer between Dy3+ and Sm3+ ions play a role in modifying the luminescence of LBW:Dy3+/Sm3+ co-doped phosphors. With a constant excitation wavelength (λ Ex), different levels of activator doping lead to a change in the emission colors from their neutral white light to a deep orange-red region for LBW:Dy3+/Sm3+ phosphors. The decay curves demonstrate a decrease in lifetime with an increase in the concentration of activator ions (Sm3+). For D3S5 phosphor, the temperature-dependent photoluminescence characteristics were analyzed under λ Ex = 336 nm excitation. The results indicate excellent luminescence thermal stability with an activation energy of 0.16 eV at λ Ex = 336 nm. With its low color-correlated temperature and good thermal stability, the prepared phosphor sample shows potential as a solid-state emitting phosphor that can be used with UV chip stimulation for warm white LED applications.

Numerical modeling of the behavior of concrete exposed to chloride ions by coupling age and mechanical stresses

This study proposes a quantitative examination of the issue of chloride ion infiltration in concrete under mechanical strain in a hostile setting while considering the influence of time, commonly referred to as the aging effect. The relationship between the diffusion coefficient and age, when subjected to specific levels of uniaxial or biaxial stresses for various W/C ratios, has allowed us to assess the concentration of chloride ions and the time needed for corrosion to begin through the coating layer in three dimensions. The numerical model results corroborate the notion that the corrosion process is affected by the fluctuation of the diffusion coefficient, which is directly linked to the age factor and the mechanical stresses exerted on the concrete. The model also emphasizes the extended distribution of chloride ion concentration at a certain depth, which is connected to the ratio of water to cement, influenced by the diffusion coefficient and the degree of mechanical stress in older structures.

Highly sensitive and selective fluorescent "turn-on" sensor for Ag+ detection using MAPbBr3@PCN-221(Fe): An efficient Ag+-bridged energy transfer from perovskite to MOF.

Metal ion-induced water pollution is attracting increasing public attention. Perovskite quantum dots and metal-organic frameworks (MOFs), owing to their outstanding properties, hold promise as ideal probes for detecting metal ions. In this study, a composite material, MAPbBr3@PCN-221(Fe), was prepared by encapsulating MAPbBr3 quantum dots with PCN-221(Fe), demonstrating high chemical stability and good reusability. The composite material shows a sensitive fluorescence turn-on signal in the presence of silver ions. The fluorescence intensity of the composite material exhibits a linear relationship with the concentration of Ag+ in the solution, with a low detection limit of 8.68 µM. Moreover, the fluorescence signal exhibits a strong selectivity for Ag+, enabling the detection of Ag+ concentration. This fluorescence turn-on signal originates from the Ag+-bridged energy transfer from the conductive band of MAPbBr3 to the excited state of the MOF, which is directly proportional to the concentration of silver ions. Simultaneously, this finding may open up a new possibility in artificial controlled energy transfer from perovskite to MOF for future development.

Role of copper chelating agents: between old applications and new perspectives in neuroscience

Abstract The role of copper element has been an Increasingly relevant topic In recent years In the fields of human and animal health, for both the study of new drugs and Innovative food and feed supplements. This metal plays an important role in the central nervous system, where it is associated with glutamatergic signaling, and it is widely involved in inflammatory processes. Thus, diseases involving copper (II) dyshomeostasis often have neurological symptoms, as exemplified by Alzheimer's and other diseases (such as Parkinson's and Wilson's diseases). Moreover, imbalanced copper ion concentrations have also been associated with diabetes and certain types of cancer, including glioma. In this paper, we propose a comprehensive overview of recent results that show the importance of these metal ions in several pathologies, mainly Alzheimer's disease, through the lens of the development and use of copper chelators as research compounds and potential therapeutics if included in multi-target hybrid drugs. Finally, seeing how copper homeostasis is important for the well-being of animals as well as humans, we shortly describe the state of the art regarding the effects of copper and its chelators in agriculture, livestock rearing, and aquaculture, as ingredients for the formulation of feed supplements as well as to prevent the effects of pollution on animal productions.

Recycling of waste coffee grounds as a photothermal material modified with ZnCl2 for water purification

The aim of this study was to develop a photothermal material modified with carbonization and ZnCl2 impregnation and supported by polyvinyl alcohol (PVA) for water purification using the waste coffee grounds. Scanning electron microscopy (SEM) characterization of the prepared material revealed that a significant surface modification was achieved due to the carbonization and ZnCl2 impregnation. X-ray diffraction analysis (XRD) pattern of the samples showed two broad peaks at 18.4° and 22.2°, this is due to the crystal planes of β-crystal phase structure, which indicates the existence of strong hydrogen bonds between the micro-structures and therefore less suspectable to chemical attack. Additionally, thermogravimetric analysis (TGA) result suggests a slight mass reduction between the temperature range of 65–75 °C implying the thermal stability of the prepared material. The produced modified material had a photothermal conversion efficiency of 74% and could produce vapor at a rate of 1.12 kg/m2h under 980 W/m2 irradiation at 1 sun. A significant reduction in Cu2+ ion concentration (83%), turbidity (91%), total dissolved solids (TDS) (61%), microbial load (95.6%), and total hardness (41.2%) were achieved. Therefore, waste coffee grounds can be considered as a future eco-friendly and low-cost candidate for water purification.

Factorial experimental design optimisation of adsorption process for removing chrome ion using crude biomass

ABSTRACT The pollution of water and the environment by heavy metals has recently increased dramatically, creating a severe environmental problem due to their non-biodegradability and high toxicity. Among these metals, we are interested in chromium (Cr), essential for human life but can be toxic in large quantities. It is vital to develop a simple, effective, and inexpensive method for its removal from aqueous media. This work aims to combine two aspects: environmental protection and waste recovery. We studied the adsorption capacity of Cr(VI) by biomass consisting of a mixture of walnut shells, pecan nuts, and peanuts. The ion was quantified using high-resolution magnetic sector inductively coupled plasma mass spectrometry, and several techniques characterised the raw adsorbent. To optimise the removal of Cr(VI), four factors were optimised using a 24-full factorial design, enabling us to determine the optimum adsorption conditions: a contact time of 360 min, an adsorbent mass of 30 mg, an initial ion concentration of 50 mg/L, and a pH of 6. The response efficiency Y (Qe) achieved its optimum at 58.47976 ± 4.168804 (mg/g), resulting in a maximum desirability of 0.957419. The adsorption phenomenon was studied kinetically, and it was found to follow the pseudo-first-order reaction (R 2 = 0.9894); concerning adsorption isotherms, the Freundlich isotherm proved to be the best (R 2 = 1). Overall, the present biosorbent demonstrates excellent capacity to remove Cr (VI) from water and can be used on a large scale.

The Effect of Calcium Ions on the Electrophysiological Properties of Single ANO6 Channels.

Proteins belonging to the anoctamin (ANO) family form calcium-activated chloride channels (CaCCs). The most unusual member of this family, ANO6 (TMEM16F), simultaneously exhibits the functions of calcium-dependent scramblase and the ion channel. ANO6 affects the plasma membrane dynamics and phosphatidylserine transport; it is also involved in programmed cell death. The properties of ANO6 channels remain the subject of debate. In this study, we investigated the effect of variations in the intracellular and extracellular concentrations of calcium ions on the electrophysiological properties of endogenous ANO6 channels by recording single ANO6 channels. It has been demonstrated that (1) a high calcium concentration in an extracellular solution increases the activity of endogenous ANO6 channels, (2) the permeability of endogenous ANO6 channels for chloride ions is independent of the extracellular concentration of calcium ions, (3) that an increase in the intracellular calcium concentration leads to the activation of endogenous ANO6 channels with double amplitude, and (4) that the kinetics of the channel depend on the plasma membrane potential rather than the intracellular concentration of calcium ions. Our findings give grounds for proposing new mechanisms for the regulation of the ANO6 channel activity by calcium ions both at the inner and outer sides of the membrane.

A New Modified Carbon Paste Electrode for Selective Determination of Chromium(III) in Pharmaceutical Drugs and Food Samples

Background and Objective: This study presents a novel potentiometric method for the precise, accurate, selective, and rapid determination of Cr(III) ion concentration in different samples. Methods: A new ionophore, namely macrocyclic tetramide ionophore (MCTA), was synthesized through an inexpensive and straightforward approach, yielding a high-quality product. The (MCTA) ionophore was utilized as the active center in the preparation of modified carbon paste electrodes (MCPEs) to quantify the Cr(III) ion. The paste was made by adding graphite, MCTA, and plasticizer and mixing them in varying weight percent ratios. Results: The proposed electrodes, I and II, exhibited a trivalent Nernstian response of 20.029 ±0.57 and 20.3±0.56 mV decade-1 , respectively, with linearity of 1.0x10-7 – 1.0x10-2 and 1.0x10-5 – 1.0x10- 2 mol L-1 . Electrodes I and II were examined for their pH, response time, and thermal stability. In comparison to other mono-, bi-, and trivalent cations, starch, and sugars, the electrodes demonstrated a high degree of selectivity for Cr(III). The modified electrodes were used to determine the concentration of Cr(III) in various real samples, including drug tablets, juice extractions, and tap water, with acceptable recovery values. Conclusion: The results were compared with those obtained using the previously reported method, with no significant difference observed between them, as indicated by the F and t-test values. The data showed good accuracy and precision, as well as a high percentage of recovery. The adsorption capacity of the MCTA ionophore towards Cr(III) ions was also examined.