Direct Determination Research Articles

An improved dual shear unified strength model (IDSUSM) considering strain softening effect

This study proposes an improved dual shear unified strength model by introducing the plastic internal variable which reflects the collective effects of strain softening, intermediate principal stress and unequal strength under tension and compression. The improved model is then simplified into simple forms for typical stress states, including uniaxial tension and compression, plane stress pure shear and tri-axial stress states. The smooth method and conjugate gradient method are utilized to facilitate its numerical implementation, avoiding numerical singularity and non-convergence in the solution process. The physical meanings of the parameters are further clarified and their values for self-compacting concrete are determined from the results of triaxial compression tests through a combination of direct determination, equation solution and back propagation (BP) neural network optimization. Validated against the test results, the improved model gives a more accurate prediction than the traditional dual shear unified strength model and Mohr-Coulomb model, in terms of both the overall trend and representative values. Validation results show that the improved model is applicable to materials for which the compressive strength is greater than the tensile strength and the tensile strength is greater than the shear strength.

Uneven changes in air and crown temperatures associated with snowpack changes affect the phenology of overwintering cereals

Time series analysis of overwintering cereals in snowy areas has revealed several phenological patterns associated with climate changes in winter. Herein, to investigate the recent effect of climatic variations on overwintering cereals, we investigated the phenology over multiple decades at three snowy region sites with an air temperature (Tair) increase trend of 0.48–1.09 °C/decade. Our findings were as follows: heading trends differed within the same cultivar at different sites; phenology was promoted with increasing temperatures in cooler regions and decreasing snow duration in regions with heavy snow; crown temperature (Tcrown) was a more direct determinant than Tair in phenology estimation model in regions with heavy snow. A thermal gap of more than a few degrees Celsius between Tair and Tcrown, owing to the insulation effect of snowpack, affected the phenology of overwintering cereals. A shorter snow cover period promoted phenology in locations with temperatures >0 °C. Subsequently, we found that when the thermal gap was >0 °C of the growing temperature range, Tcrown directly helped determine the phenology of overwintering cereals, and irrespective of the warming trend, the periodic inflow of cold air into the northern mid-latitudes of the Northern Hemisphere and associated snow cover changes dominated Tcrown, resulting in annual phenological anomalies with a range of fluctuations of approximately 1 month. The trend of increasing Tair during spring in northern Japan is consistent with the global trend, with a pronounced trend of advancing phenology reaching >4 days/decade in a typical cooler location experiencing snowmelt in March.

Practical high-resolution spectroscopy with a spatial heterodyne spectrometer: Determination of instrumental function for lineshape recovery

The spatial heterodyne spectrometer (SHS) is a well-recognized platform for its high resolving power in various use cases of spectroscopy. Same as other spectrometer topologies, the SHS, unfortunately, also suffers from classical challenges such as distorted lineshape due to the instrumental function. The goal of this work is to tackle this persisting issue through a simple numerical approach. With the inherent characteristics of an SHS interferogram, we report the direct extraction and determination of the instrumental function in its numerical representation from an SHS interferogram; this instrumental function was further used for spectral data processing that enables significant improvements in spectral resolution through deconvolution algorithms.Here, we systematically discuss the recognition of the embedded instrumental function among various ingredients within an interferogram. To verify the numerical approach, lithium was chosen as the model sample, resembling the use of SHS in an isotopic analysis application. Specifically, the resonance transition of lithium D-lines (2P1/2,3/2 ← 2S1/2) was selected to assess the performance of the spectral processing. With the spectral deconvolution, the spectral features that represent the 6Li and 7Li were nearly baseline-separated, allowing for the accurate measure of the isotopic abundance without external references or algorithm adjustments (e.g., curve fitting).

Direct determination of chronic myeloid leukemia prevalence in Lombardy-Italy: Global implications.

Lombardy represents the largest region of Italy by population, with almost 10 million residents, a dimension similar to a medium size country like Sweden or Belgium. The CML subcommittee of the Lombardy Hematology Network (REL-CML) conducted a study at the beginning of 2023. Prevalence was calculated by direct input from the 21 centers participating in REL-CML. Tyrosine Kinase Inhibitors (TKI) prescription records collected from the ARIA regional registry were used to estimate the number of CML patients followed in smaller centers not participating in REL-CML. A total of 2285 patients were registered, representing a prevalence of 0.23 ‰. These data were compared to a similar census conducted in 2005, at the beginning of the TKI era, where a prevalence of 0.029‰ was calculated. This indicates that an almost 10 times increase took place during this period of time. Imatinib represents the most frequently prescribed first-line TKI; its use in 2022 still represented 75% of total first line prescriptions. An increased concentration of the care of CML patients in specialized REL centers with a decreased dispersion of patients in small centers was also evident over this 18year period of time. Nineteen % of patients discontinued treatment, highlighting persisting logistical and biological challenges; one some recommendations on CML management are included to this aim.

Additional applications of the Lambert W function to solid state physics

Analytical solutions are always desirable in physics for the sake of mathematical exactness and physical insight. In this study, I obtain closed-form analytical expressions for various physical quantities taken from solid state physics. More precisely, I derive analytical expressions in terms of the Lambert W function for the work function and the field-enhancement factor of a field emitting material from the Fowler–Nordheim equation. Additionally, I derive similar analytical expressions for the localization length and the density of states in amorphous semiconductors from the Mott hopping conductivity. Similarly, I also derive analytical formulae based on the Lambert W function to compute the extrinsic-intrinsic transition temperature in a partially compensated semiconductor and the Kondo exchange coupling constant. All the obtained results are exact and explicit. Moreover, some of them allow a direct determination of some physical quantities of interest compared to their indirect determination from semi-logarithmic experimental plots. The findings of this paper are accessible and suitable for students enrolled in graduate solid state physics courses.

The moss growth optimization (MGO): concepts and performance

Abstract Metaheuristic algorithms are increasingly utilized to solve complex optimization problems because they can efficiently explore large solution spaces. The moss growth optimization (MGO), introduced in this paper, is an algorithm inspired by the moss growth in the natural environment. The MGO algorithm initially determines the evolutionary direction of the population through a mechanism called the determination of wind direction, which employs a method of partitioning the population. Meanwhile, drawing inspiration from the asexual reproduction, sexual reproduction, and vegetative reproduction of moss, two novel search strategies, namely spore dispersal search and dual propagation search, are proposed for exploration and exploitation, respectively. Finally, the cryptobiosis mechanism alters the traditional metaheuristic algorithm’s approach of directly modifying individuals’ solutions, preventing the algorithm from getting trapped in local optima. In experiments, a thorough investigation is undertaken on the characteristics, parameters, and time cost of the MGO algorithm to enhance the understanding of MGO. Subsequently, MGO is compared with 10 original and advanced CEC 2017 and CEC 2022 algorithms to verify its performance advantages. Lastly, this paper applies MGO to four real-world engineering problems to validate its effectiveness and superiority in practical scenarios. The results demonstrate that MGO is a promising algorithm for tackling real challenges. The source codes of the MGO are available at https://aliasgharheidari.com/MGO.html and other websites.

Total organic carbon quantification in soils and sediments: Performance test of a modified sample preparation method

The total organic carbon (TOC) concentration of particulate samples is a key parameter to characterize soils and sediments. To demonstrate the applicability and reliability of a modified sample preparation method for the direct measurement of TOC contents in suspended particulate samples, we analyzed five certified reference materials (CRMs) with varying TOC concentrations using a Shimadzu TOC-L CPH analyzer. Measured values were calibrated with a multi-point curve that cover the full range of the expected TOC concentrations and the results were validated using statistical values and measures. The method validation reveals that the measurements are accurate and precise for CRMs from marine and soil contexts, but show a low accuracy for the CRM containing polycyclic aromatic hydrocarbons (PAHs). This demonstrates the applicability and reliability of the modified preparation method for direct TOC determination of suspended particulate samples. Therefore, it is relevant for a broader community, beyond geosciences, and for users employing devices of other manufacturers to analyze TOC in suspended particulate samples.•Modified preparation method uses reduced sample weights and yields accurate and precise results.•Cost-efficient and environmentally friendly alternative: reduces waste by saving acid and ultrapure water.•Avoids incomplete dissolution of dolomite by heating acidified samples.

Research on Strategies for Enhancing the Ideological and Political Education Ability of College Counselors under the New Situation: A Case Study of Wenzhou Polytechnic

With the rapid development of higher vocational education, higher vocational colleges play a more and more important role in training high-quality technical talents and serving regional economic development. In this context, as the backbone of ideological and political education of students in higher vocational colleges, counselors bear the heavy responsibility of guiding students to shape a correct world outlook, outlook on life and values. The construction of their team is not only related to the depth and breadth of students' ideological and political education, but also a direct determinant of the effectiveness of ideological and political education. Under the new historical conditions, it has become an urgent task to strengthen the ideological and political education ability of counselors in higher vocational colleges. This paper is committed to analyzing the current situation of ideological and political education of counselors in higher vocational colleges under the new situation, and deeply discussing how to improve the ideological and political education quality of counselors in multiple dimensions.

Determination of chromium traces by atomic ionization spectroscopy in aqueous standard solutions and in gallium arsenide using the «rod – flame» atomization system

The results of the determination of trace amounts of chromium in aqueous standard solutions of chromium and in high purity gallium arsenide using atomic ionization spectroscopy are presented. Single — and two-step schemes of chromium atom excitation from the ground state 3d54s 7S3 to septet states 3d54p 7P2,3,4, 3d44s4p 7P2,3,4 were studied using a «rod – flame» atomizer. A mechanism of forming atomic-ionization signal for two-step excitation schemes is revealed. The most effective two step excitation schemes for chromium atoms were determined and experimentally studied at different wavelengths λ1 = 425.4 nm, λ2 = 451.4 nm; λ1 = 425.4 nm, λ2 = 426.1 nm. The low limit of chromium detection in aqueous water solutions was 50 pg/ml. The analytical potentiality of the «rod – flame» system for determining traces of chromium in gallium arsenide solutions has been demonstrated. The possibility of determining traces of chromium in gallium arsenide using a flame – rod atomizer at a level of 5 × 10–7 % is demonstrated. Two methods are proposed to increase the selectivity and sensitivity of atomic-ionization determination of chromium: optimization of the temperature program of the flame – rod atomizer and the use of two-stage excitation of chromium atoms. It is shown that the main interfering factor is the background attributed to the matrix ionization. Methods are proposed to reduce or eliminate the matrix impact, which ensure direct determination of elements in samples.

Refining Children's exposure assessment to NO2, SO2, and O3: Incorporating indoor-to-outdoor concentration ratios and individual daily routine

Exposure to air pollutants like sulfur dioxide (SO2), nitrogen oxides (NOx), and ozone (O3) is associated with adverse health effects, particularly with exacerbations of asthma symptoms and new asthma cases in both children and adults. While fixed-site monitoring (FSM) stations are commonly used in air pollutant exposure studies, they may not fully capture personal exposures due to limitations such as inadequate consideration of daily routines and indoor/outdoor concentration variations. In this study, to enhance the accuracy of personal exposure calculated by using FSM data, individual's daily activity routine, encompassing both indoor and outdoor environments, were incorporated by using indoor-to-outdoor concentration ratios. Three methodologies were compared to assess the accuracy of exposure calculations: (i) direct exposure determination employing passive samplers (PS), (ii) personal exposure calculated using FSM data alone, and (iii) personal exposure calculated using FSM data refined by integrating local average individual daily activity routines and indoor-to-outdoor ratios. The results demonstrate that the refined method (iii) yields substantial improvements in estimated exposure levels, reducing the average error from 1.4% to 0.4% for NO2, from 72.1% to 12.7% for SO2, and from 323.4% to 24.9% for O3.

Comparison and review of international guidelines for treating asthma in children.

Asthma, the most common chronic disease, is characterized by airway inflammation and airflow obstruction. The World Health Organization estimates that approximately 300 million people worldwide have asthma, 30% of whom are pediatric patients. Asthma is a major cause of morbidity that can lead to hospitalization or death in severe pediatric cases. Therefore, it is necessary to provide children with objective and reliable treatment according to consistent guidelines. Several institutes, such as the Global Institute for Asthma, National Heart, Lung, and Blood Institute, British Thoracic Society, Japanese Society of Pediatric Allergy and Clinical Immunology, and Korean Academy of Asthma, Allergy, and Clinical Immunology have published and revised asthma guidelines. However, since recommendations differ among them, confusion persists regarding drug therapy for pediatric asthma patients. Additionally, some guidelines have changed significantly in recent years. This review investigated the latest changes in each guideline, compared and analyzed the recommendations, and identified the international trends in pediatric asthma drug therapy. The findings of this review may aid determinations of the future direction of the Korean guidelines for childhood asthma.

Substrate-Based Ligand Design for Phenazine Biosynthesis Enzyme PhzF.

The phenazine pyocyanin is an important virulence factor of the pathogen Pseudomonas aeruginosa, which is on the WHO list of antibiotic resistant "priority pathogens". In this study the isomerase PhzF, a key bacterial enzyme of the pyocyanin biosynthetic pathway, was investigated as a pathoblocker target. The aim of the pathoblocker strategy is to reduce the virulence of the pathogen without killing it, thus preventing the rapid development of resistance. Based on crystal structures of PhzF, derivatives of the inhibitor 3-hydroxyanthranilic acid were designed. Co-crystal structures of the synthesized derivatives with PhzF revealed spacial limitations of the binding pocket of PhzF in the closed conformation. In contrast, ligands aligned to the open conformation of PhzF provided more room for structural modifications. The intrinsic fluorescence of small 3-hydroxyanthranilic acid derivatives enabled direct affinity determinations using FRET assays. The analysis of structure-activity relationships showed that the carboxylic acid moiety is essential for binding to the target enzyme. The results of this study provide fundamental structural insights that will be useful for the design of PhzF-inhibitors.

Refined determination of the weak mixing angle at low energy

The weak mixing angle is a fundamental parameter of the electroweak theory of the standard model whose measurement in the low-energy regime is still not precisely determined. Different probes are sensitive to its value, including atomic parity violation, coherent elastic neutrino-nucleus scattering, and parity-violating electron scattering on different nuclei. In this work, we attempt for the first time to combine all these various determinations by performing a global fit that also takes into account the unavoidable dependence on the experimentally poorly known neutron distribution radius of the nuclei employed, for which a new measurement using proton-cesium elastic scattering became available. By using all present direct determinations of the neutron distribution radius of cesium, we find sin2ϑW=0.2396−0.0019+0.0020, which should supersede the previous value determined from atomic parity violation on cesium. When including electroweak only, but also indirect, determinations of the neutron distribution radius of cesium, the uncertainty reduces to 0.0017, maintaining the same central value and showing excellent agreement independently of the method used. Published by the American Physical Society 2024

Direct Determination of POSS Cage Structure in a Self-Assembled Ionic Bridged Silsesquioxane by Using the Total Pair Distribution Function G(r) and Density Functional Theory.

In the present study, both short-range and long-range structural features of an ionic bridged silsesquioxane, specifically one containing the 1,4-diazoniabicyclo[2.2.2]octane chloride group (ISSQ), were elucidated. This ionic silsesquioxane was synthesized via direct polycondensation of a bridged organosilane precursor, without any additional functionalization step. Si-O-Si cage structures typical of Polyhedral Oligomeric Silsesquioxanes (POSS) were identified. The average interatomic distances of the POSS cages, including the open T8 cage and the T12 cage for the ISSQ, as well as the T8 cage for a commercially available pendant POSS were determined. It is the first report of the interatomic distance determination of POSS cage; achieved by using total pair distribution function G(r) values obtained through high-resolution synchrotron X-ray diffraction combined with density functional theory (DFT) calculations. The application of DFT was crucial for accurately assigning X-ray peaks and verifying structural details. Furthermore, the analysis of X-ray diffraction peaks and the examination of crystalline domains via transmission electron microscopy enabled the proposal of a hexagonal arrangement of Si-O-Si cages over long ranges within the ionic bridged silsesquioxane. This proposed arrangement highlights a distinctive structural organization that could impact the material's properties and applications.

Development of novel electrochemical sensor based on Co-Fe layered double hydroxide for simultaneous determination of Hydroquinone, Catechol, and Resorcinol

In this work, a novel electrochemical sensor was developed using a glassy carbon electrode modified with Co-Fe-layered double hydroxides (Co/Fe-LDH/GCE) for the detection of dihydroxybenzene isomers (Hydroquinone (HQ), Catechol (CC), and Resorcinol (RS) due to the large active surface area, facile electronic transport, and high electrocatalytic activity features of LDH. X-ray diffraction (XRD), X-ray energy dispersive spectroscopy (EDX), and scanning electron microscopy (SEM) techniques were used to characterize the modifier. Under the optimized conditions, the differential pulse voltammetry (DPV) method was used as a sensitive and efficient method to measure dihydroxybenzene isomers. Well-separated oxidation peak potentials corresponding to HQ, CC, and RS were observed at 0.04 V, 0.150 V, and 0.560 V, respectively. The linear range was 2.5 × 10−9 to 1.2 × 10−5 M for hydroquinone and catechol and 7.5 × 10−9 to 4.2 × 10−6 M for resorcinol, with a detection limit of 0.001, 0.001, and 0.005 µM (S/N=3) for hydroquinone, catechol, and resorcinol, respectively. The Co/Fe-LDH sensor demonstrated a fast response, high sensitivity, excellent stability, and satisfactory repeatability. The modified electrode was successfully applied to the direct determination of DBIs in river water, providing reliable recovery data.

Counterion Distribution in the Stern Layer on Charged Surfaces.

Counterion adsorption at the solid-liquid interface affects numerous applications. However, the counterion adsorption density in the Stern layer has remained poorly evaluated. Here we report the direct determination of surface charge density at the shear plane between the Stern layer and the diffuse layer. By the Grahame equation extension and streaming current measurements for different solid surfaces in different aqueous electrolytes, we are able to obtain the counterion adsorption density in the Stern layer, which is mainly related to the surface charge density but is less affected by the bulk ion concentration. The charge inversion concentration is further found to be sensitive to the ion type and ion valence rather than to the charged surface, which is attributed to the ionic competitive adsorption and ion-ion correlations. Our findings offer a framework for understanding ion distribution in many physical and chemical processes where the Stern layer is ubiquitous.

Simultaneous spectrophotometric and chromatographic determination of Ketorolac and Dexamethasone: Overall assessment regarding environmental Impact, Practicality, and functionality principles

Determination of a drug combination that contains a minor component that is also a poorly UV absorbing analyte represents greet challenges in drug analysis. A fixed-dose ophthalmic combination of ketorolac tromethamine (KET) and dexamethasone sodium phosphate (DEX) (in the ratio of 5:1) is used to relieve post-surgical inflammation and seasonal allergic conjunctivitis due to their analgesic and anti-inflammatory activity. Five spectrophotometric methods and a reversed phase chromatographic separation method were developed and validated for simultaneous determination of both drugs in lab-prepared eye drops. Direct spectrophotometric determination of KET (the major, highly UV absorbing analyte) was achieved from the zero-order UV absorption spectra at 323 nm while DEX (which is the minor, poorly UV absorbing analyte) was quantified after applying several spectrophotometric methods. Either fundamental zero-order spectra or ratio spectra were used, and measurements were done at either single or dual wavelengths. The developed methods were: isosbestic point method, absorption factor method, dual wavelength method, ratio difference UV spectrophotometric method, and simultaneous equation method. The developed spectrophotometric methods determine KET in the linearity range of 2.0–12.0 μg/mL and DEX in the range of 5.0 – 35.0 μg/mL. For accurate spectrophotometric determination of DEX in the ratio of the dosage form, multiple standard addition method was applied. HPLC technique was also applied for separation and quantification of both drugs. Chromatographic separation was attained by using Hypersil ODS-C18 (150 x 4.6 mm, 5 μm) column. The mobile phase was composed of 50 % methanol: 50 % phosphate buffer (pH 2.5). The column compartment was maintained at 25 °C. Flow rate was adjusted at 1.2 mL/min and detection was performed by DAD at 254 nm. The linearity of HPLC method was 5.0–100.0 μg/mL, and 5.0–50.0 μg/mL for KET and DEX, respectively. Simultaneous determination of both drugs was applied to lab-prepared eye drops that contain also benzalkonium chloride as inactive ingredient. The developed methods determined the cited drugs with good and acceptable % recovery. The results of the developed methods and a reported HPLC method were compared using one-way ANOVA test, F-test and student’s t-test at confidence level 95 %, and they show no significant statistical difference. Assessment of greenness of the developed methods in comparison with reported HPLC method was performed using different tools, including analytical eco-scale, GAPI and AGREE. HPLC-EAT was also performed to ensure greenness of developed HPLC method. Moreover, assessment of practicality, applicability, and functionality of developed and reported methods was evaluated by BAGI metric tool and WAC calculator, respectively. The developed methods allow simple, rapid, and accurate analysis of quality control samples that contain KET and DEX.

Development and experimental evaluation of hybrid K-edge/X-ray fluorescence densitometer for uranium solution measurement

The hybrid K-edge/X-ray fluorescence densitometer (HKED) is a combination of K-edge absorption technology (KED) and characteristic X-ray fluorescence (XRF), which has the advantages of direct, fast and non-destructive determination, and is an ideal non-destructive measurement technology for uranium and plutonium concentrations. In this paper, a new HKED was developed, primarily utilizing an X-ray tube from COMET, alongside high-purity germanium (HPGe) and cadmium telluride (CdTe) detectors from AMETEK ORTEC. This manuscript delves into several variables that influence measurement outcomes under predefined experimental conditions and operational prerequisites to pinpoint critical parameters. It was discerned that the adoption of a 160 kV high voltage setting markedly diminishes experimental interferences, while the beam current, optimally set at 2 mA, not only ensures a linear correlation with the count rate but also maximizes the effective count detected. The incorporation of a 2 cm fixed-length iron rod along the trajectory between the sample and the detector, complemented by an additional 3 mm external absorber before the KED detector, effectively mitigates direct X-ray exposure, thereby enhancing transmittance values to attainable extents. Subsequent to the determination of these pivotal parameters, validation of the HKED system's efficacy was conducted via performance evaluation tests on a laboratory-scale HKED setup. Measurements undertaken for both KED and XRF across an interval ranging from 300 to 3000 s fell within the 2σ boundary, affirming the system's stability. Repeated measurements of 50 g/L and 150 g/L uranium solutions yielded KED precision rates of 0.56% and 0.19%, respectively. Moreover, linear regression analyses linking transmittance, characteristic X-ray fluorescence, and uranium concentrations across a spectrum of 0–150 g/L underscored the laboratory HKED instrument's robust analytical capabilities. Notably, the relative discrepancy between theoretical predictions and empirical findings for the 150 g/L uranium sample was minimized to a commendable 0.58%.

Characterization of Proton Exchange in Protonic Ceramic Electrochemical Cells Using Operando Drifts

The protonic ceramic electrochemical cells (PCECs) have attracted tremendous attention for their fast hydrogen production at intermediate temperatures. This work applied in situ Diffuse reflectance infrared Fourier transform infrared spectroscopy (DRIFTS) together with electrochemical impedance spectroscopy (EIS), to characterizes transport and hydration properties of the state-of-the-art electrolyte materials. The adsorption of water molecules and formation of surface hydroxyl groups on the electrolyte surface as a function of temperature, steam concentration, and electrical potential were systematically investigated by DRIFTS under operando conditions. The quantitative information on the concentration of hydroxyl species on the electrolyte materials before and after exposure to steam were obtained. The determination of OH intensity leads to the direct determination of the proton exchange coefficient k, at different steam concentrations and biases. The results are unique and should be able to provide valuable insights into the mechanisms of proton formation, migration, and evolution under various operating conditions, which is critical to design better electrolyte compositions and optimize the operation conditions for next-generation PCECs.

Highly selective and sensitive potentiometric determination of favipiravir in COVID-19 antiviral drug formulations

In this study, a novel all-solid-state electrochemical sensor based on favipiravir-tetraphenylborate (FAV-TPB) electroactive material was developed and reported for FAV’s highly selective and sensitive potentiometric determination in COVID-19 antiviral drug formulations. All-solid-state FAV selective sensor was fabricated by mixing and properly pressing FAV-TPB, graphite (G), multi-walled carbon nanotube (MWCNT), and paraffin oil (PO). In order to obtain the best sensor response, the sensor component ratios were optimized. The most satisfying response characteristics was obtained with the sensor composition FAV-TPB:G:MWCNT:PO in the ratio 32.5:42.5:5:20 (w/w %). The developed sensor displayed a wide linear near-Nernstian response to FAV over the concentration of 1.0 × 10−6 − 1.0 × 10−1 molL−1 with a slope of 53.6 ± 1.4 mV (R2 = 0.9997). The detection limits of the sensor was calculated as 6.0 × 10−7 molL−1, respectively. The dynamic response time of the sensor was 7 s, and the sensor exhibited fairly reproducible potentiometric responses. In the pH range of 6.0–8.0, the sensor’s potential response was not affected by the pH change of the test solutions. The improved sensor had a wide temperature tolerance, and its response remained unchanged in the 10–40 ℃ temperature range. The interference effect of some chemical and biological species was evaluated by the matched potential method and separate solution method. The sensor worked stable for 12 weeks without any considerable change in its potential response. The analytical applications of the sensor were successfully carried out with the potentiometric titration of FAV with sodium tetraphenylborate solution and also the direct determination of favipiravir in COVID-19 antiviral drug formulations.