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In this research, the solubility of amlodipine besylate was studied in the propylene glycol + ethanol mixtures at different temperatures (293.2–313.2 K). The study showed that the solubility increases with an increase in propylene glycol concentration, reaching its highest point at w1 = 0.8. Additionally, the solubility values have a positive correlation with temperature, which is typical for the solid solutes. The experimental solubility data were correlated with some well known cosolvency models and the accuracy of these models was investigated with the mean relative deviations (MRDs%) of the back-calculated data. MRDs were 1.2% for the van't Hoff model, 4.3 and 4.6% for the Jouyban–Acree and Jouyban–Acree–van't Hoff equations, 1.4% for the MRS model and 2.1% for the modified Wilson model. The apparent thermodynamic parameters (standard state Gibbs energy, enthalpy, and entropy) of dissolution of ADB in the non-aqueous saturated mixtures were also calculated with the van't Hoff and Gibbs equations at Thm = 303.0 K. [ABSTRACT FROM AUTHOR]

The increasing demand for sustainable chemical processes has led to the exploration of binary mixtures of ionic liquids (ILs) and cyclic ethers (CEs) as alternative solvent systems. This paper examines the environmental impacts, economic feasibility, and future implications of these mixtures. The environmental benefits of IL-CE mixtures include reduced toxicity, enhanced biodegradability, and lower overall ecological footprints compared to traditional solvents. Economically, while initial production costs may be higher, operational efficiencies, waste reduction, and potential market growth present compelling arguments for their adoption. Future implications highlight the importance of interdisciplinary research, regulatory developments, and innovations in synthesis and formulation. As industries move towards greener practices, understanding the full potential of IL-CE mixtures is essential for advancing sustainability in the chemical sector. [ABSTRACT FROM AUTHOR]

To unravel the intricacies of two-phase gas-liquid flow characteristics and heat transfer behavior, an array mini-channel gravity plate heat pipe (AMGPHP) is proposed in this work, which allows for observing the internal changes in the state of the working fluids. The flow patterns such as pool flow, columnar flow, and slug flow, are experimentally explored and analyzed in detail. It is found that the optimal volume fill ratio is 20% by utilizing start-up time and thermal resistance as performance evaluation metrics. With this fill ratio, a medium optimization strategy by blending ethanol within R141b is proposed and evaluated. In comparison to pure working fluids, the heat transfer performance of AMGFHP in the binary fluid has been significantly augmented due to temperature and concentration shifts resulting from disparate boiling points. Under the 10% volume fraction ethanol blending condition, the equivalent thermal conductivity of the heat pipe is dramatically elevated, with a value of 3110 W/(m·°C), along with the reduction of the minimum start-up power to 4 W. In general, applying such a medium to heat pipes has considerable potential in practical applications. [ABSTRACT FROM AUTHOR]

This paper reports new experimental data involving density (ρ), viscosity (η), and ultrasonic velocity (u) for four binary mixtures consisting of methyl methacrylate (MMA) with heptane, decane, dodecane, and tridecane at temperatures 303.15, 308.15, and 313.15 K and atmospheric pressure measured over entire composition range. The experimental data have been used to calculate excess or deviation parameters such as excess molar volume , deviation in viscosity (Δη) and the acoustical parameters namely isentropic compressibility (Ks), free volume (Vf), free length (Lf), and internal pressure (πi). The excess or deviation properties have been fitted to the Redlich–Kister polynomials and the variation of these parameters with composition were discussed from the viewpoint of molecular interactions prevailing in the mixtures. The properties reported are found to be either positive or negative depending upon nature of liquid mixture and associated molecular interactions of the binary mixtures. [ABSTRACT FROM AUTHOR]

In recent years, the presence of Pharmaceutical Active Compounds (PhACs) in ecosystems has become a serious environmental problem due to their capacity to induce harmful effects at extremely low concentrations in both humans and wildlife. Water treatment plants have not been designed to remove these types of compounds efficiently. Thus, the detection of these pollutants is essential to evaluate their negative impacts and is one of the emerging issues in environmental chemistry. The main objective of this study is to determine the bacterial toxicity of two PhACs (both individually and as a mixture) through the quantification of bioluminescence inhibition in the marine bacteria Aliivibrio fischeri, a commonly used method in short-term toxicity tests. In this work, Acetaminophen and Edaravone, two drugs approved by the Food and Drug Administration, have been studied. The acute toxicity of these PhACs has been tested at two exposure times (5 and 15 min) and different concentrations, by estimation of the median effective concentration (EC50) for each individual compound or in combination at different concentrations. Moreover, the EC50 of the binary mixtures Acetaminophen/Edaravone have been forecast using two traditional predictive models, Concentration Addition and Independent Action. The results show that toxicity decreases with exposure time and depends on the concentration tested. Furthermore, a novel semi-empirical Van Laar-based model has been proposed and validated with the experimental data from this study and literature data, obtaining satisfactory estimations of the EC50 for binary mixtures. Highlights: The bacterial toxicity of Acetaminophen and Edaravone, as well as their binary mixtures, was evaluated using an Aliivibrio fischeri bioluminescence assay. The predictive power of Concentration Addition and Independent Action models was evaluated for combined bacterial toxicity of PhACs. A new semi-empirical Van Laar-based model was developed and validated to predict the bacterial toxicity of binary mixtures of Acetaminophen and Edaravone, providing accurate estimations with limited experimentation. [ABSTRACT FROM AUTHOR]

The article is an erratum for a previous publication that introduced the CompSol database, which contains solvation energy data. The erratum states that anomalies were detected in the database, specifically in the solvation energies of pure species. The errors were found to be caused by incorrect calculation procedures and the number of temperatures considered for each pure species. The authors corrected the errors and updated the database using a recent version of the DIPPR801 databank. The conclusions reached in the original publication remain unchanged. The corrected versions of the figures from the original publication are provided in the erratum. The CompSol database is available as an Excel file, containing separate spreadsheets for pure components and binary mixtures. [Extracted from the article]

Copyright of Baghdad Science Journal is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Describing fat phase behavior is of significant interest for food and non-food applications. One recognized approach to understand the behavior of complex fatty systems is to simplify the fat matrix and to emphasize only the main triacylglycerol (TAG) components. In this context, the kinetic phase behavior and phase transformation paths of binary mixtures of selected saturated monoacids (trilaurin (LaLaLa), trimyristin (MMM), and tripalmitin (PPP)) and of mixed saturated triacylglycerols containing lauric (La) and myristic (M) acids (MMLa and LaLaM) typical from lauric fats were investigated. Kinetic phase diagrams were constructed based on DSC heating thermograms (fast cooling and reheating at 5 °C min−1) and powder X-ray diffraction data. The investigated binary kinetic phase diagram presented an apparently typical eutectic behavior, with a eutectic point that varies depending on the blend composition. Introducing mixed saturated TAGs (MMLa or LaLaM) in binary blends led to a shift in the position of the eutectic point. Considering the binary blends made of LaLaLa, it was shifted from XLaLaLa = 0.7 in the LaLaLa–MMM system to XLaLaLa = 0.5 for the LaLaLa–MMLa mixture, and to XLaLaLa = 0.25 for the LaLaLa–LaLaM blend. Finally, the blend made of the two mixed TAGs (MMLa–LaLaM) also presented a complex non-ideal behavior. [ABSTRACT FROM AUTHOR]

In the current context of increasing energy demand, ionic liquids (ILs) are presented as possible candidates to replace conventional electrolytes and to develop more efficient energy storage devices. The IL 1-Methyl-1-propylpyrrolidinium bis(trifluoromethanesulfonyl)imide has been selected for this work, due to the good thermal and chemical stabilities and good electrochemical performance of the pyrrolidinium cation based ILs. Binary mixtures of this IL and lithium salt with the same anion, [TFSI], have been prepared with the aim of assessing them, as possible electrolytes for lithium batteries. These mixtures were thermally and electrochemically characterised through DSC and dielectric spectroscopy studies. The ionic conductivity decreases as the salt concentration increases, finding values ranging between 0.4 S/m and 0.1 S/m at room temperature. Additionally, a wide liquid range was found for the mixtures, which would reduce or even eliminate some of the most common problems of current electrolytes, such as their crystallisation at low temperatures and flammability. Finally, the toxicity of pure IL and the intermediate salt concentration was also evaluated in terms of the bioluminescence inhibition of the Alivibrio Fischeri bacteria, observing that, although the toxicity increases with the salt addition, both samples can be classified as practically harmless. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Faculty of Pharmacy of Ankara University / Ankara Üniversitesi Eczacilik Fakültesi Dergisi is the property of Ankara University and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Mass transfer through fluid interfaces is an important phenomenon in industrial applications as well as in naturally occurring processes. In this work, we investigate the mass transfer across vapor–liquid interfaces in binary mixtures using molecular dynamics simulations. We investigate the influence of interfacial properties on mass transfer by studying three binary azeotropic mixtures known to have different interfacial behaviors. Emphasis is placed on the effect of the intermolecular interactions by choosing mixtures with the same pure components but different cross-interactions such that different azeotropic behaviors are obtained. The molar flux is created by utilizing a non-stationary molecular dynamics simulation approach, where particles of one component are inserted into the vapor phase over a short period of time before the system's response to this insertion is monitored. From a direct comparison of the density profiles and the flux profiles in close proximity to the interface, we analyze the particles' tendency to accumulate in the interfacial region throughout the different stages of the simulation. We find that for mixtures with strong attractive cross-interactions, the inserted particles are efficiently transported into the liquid phase. For systems with weak attractive cross-interactions, the inserted particles show a tendency to accumulate in the interfacial region, and the flux through the system is lower. The results from this work indicate that the accumulation of particles at the interface can act as a hindrance to mass transfer, which has practical relevance in technical processes. [ABSTRACT FROM AUTHOR]

The present work demonstrates the accessibility of the Fick diffusion coefficient D11 and/or the thermal diffusivity a of the binary mixtures dicyclohexylmethane/diphenylmethane, n-hexane/carbon dioxide, 1-hexanol/carbon dioxide, and methane/propane by the analysis of the dynamics of non-equilibrium fluctuations using the shadowgraph method. It is evidenced that D11 and a can be simultaneously determined for binary mixtures with Lewis numbers Le = a/D11 ranging over two orders of magnitude down to Le ≈ 5 or in the presence of minor advection for binary mixtures possessing a negative Soret coefficient in the investigated temperature and pressure ranges from (298.15 to 473.15) K and from about (0.5 to 25) MPa. The determined diffusivities are compared with those measured by heterodyne dynamic light scattering or obtained from the literature, with a focus on achievable uncertainties. By this comparison, it is shown that the determination of a by the shadowgraph method was hindered by mode-coupling effects for Le ≈ 5, whereas a determination of D11 was always possible for mixtures with Le ≥ 5. Furthermore, it is demonstrated that even in the presence of solutal advection, the description of the purely diffusive behavior of non-equilibrium fluctuations in concentration remains valid. [ABSTRACT FROM AUTHOR]

The line tension of two immiscible liquids under two-dimensional and quasi-two dimensional conditions is calculated as a function of temperature, using mesoscale numerical simulations, finding that it decays linearly. The liquid–liquid correlation length, defined as the thickness of their interface, is also predicted as the temperature is varied, and it diverges as the temperature becomes close to the critical temperature. These results are compared with recent experiments on lipid membranes and good agreement is obtained. The scaling exponents of the line tension (μ) and the spatial correlation length (ν) with temperature are extracted, finding that they fulfill the hyperscaling relationship, μ = d − 1 ν , where d is the dimension. The scaling of specific heat with temperature of the binary mixture is obtained as well. This is the first report of the successful test of the hyperscaling relation between μ and ν for d = 2 and for the non-trivial case of quasi-two dimensions. This work can help to understand experiments that test properties of nanomaterials using simple scaling laws, without needing to know specific chemical details of those materials. [ABSTRACT FROM AUTHOR]

Thermochromic sensors employing cholesteric liquid crystal droplets offer customizable temperature and spectral responses through molecular adjustments of nematic mesogens. Embedded in a polymer matrix, these portable sensors enable direct, reversible temperature visualization on the skin, demonstrating potential for advanced sensing applications. [Display omitted] Rapid and accurate detection and visualization of temperature variations near the human body hold significant importance. This study presents thermochromic colloids capable of adjusting the detectable temperature range and reflection wavelength over a wide spectrum. The systematic investigation focuses on understanding the influence of the molecular structure of nematic mesogens on the morphological dynamics of cholesteric liquid crystal droplets and their associated thermochromic behaviors. A tunable colorimetric temperature range (i.e., from 10 to 40 °C) and high sensitivity (i.e., Δ λ Δ T −1 > 100nm °C−1) are realized through precise modulation of the alkyl chain lengths in cyanobiphenyls molecules, combined with a cholesteryl oleyl carbonate as a chiral dopant. We demonstrate the efficiency of a binary mixture of different mesogens, enabling customized structural colors with desired temperature responses. Finally, inspired by the ability of the octopus to camouflage through the elongation or contraction of its pigment cells, thermochromic droplets are embedded within a polymer matrix, resulting in a portable skin patch that offers quick, reversible, and direct temperature visualization of the human body. [ABSTRACT FROM AUTHOR]

A polemic is given regarding several of the volumetric properties that Touazi and coworkers reported in their published paper. A critical analysis of the published excess molar volumes for binary decalin + tridecane and decalin + tetradecane mixtures revealed that the values determined at low decalin mole fraction compositions were not consistent with values measured at higher decalin compositions. The analysis further showed that the excess molar volumes for the decalin + tridecane and decalin + tetradecane systems differ significantly from published data reported by independent research groups for binary decalin mixtures containing both smaller (C5 to C12) and larger (C16) linear alkane molecules. [ABSTRACT FROM AUTHOR]

The density and viscosity of the pseudo-binary mixtures of eutectic solvent (ES) composed of choline chloride and ethylene glycol ([ChCl/EG]) with dimethylsulfoxide (DMSO) were measured. In order to understand the effect of the mole ratio of ChCl:EG, two ChCl/EG ESs with the mole ratio of 1:3 and 1:4 (abbreviated as [ChCl/EG](1:3) and [ChCl/EG](1:4) in this work) were prepared. The measurements were carried out by digital vibrating U-tube density meter and Ubbelohde capillary viscometer from 303.15 to 323.15 K at atmospheric pressure (98.5 kPa). The Jouyban–Acree model was applied to correlate the experimental density and viscosity data of DMSO/[ChCl/EG](1:3) and DMSO/[ChCl/EG](1:4) mixtures. In addition, based on the experimental data, the derived properties of the mixtures, such as excess molar volume and viscosity deviation, were calculated. The comparison and analysis of excess molar volume and viscosity deviation for DMSO/[ChCl/EG](1:2) reported in literature and the results obtained in this work were carried out. [ABSTRACT FROM AUTHOR]

Cinnamomum verum (Cinnamomum zeylanicum or Ceylon cinnamon) is an aromatic medicinal plant, popularly used as a culinary spice and in various herbal commodities. The increasing demand and high economic value make C. verum a vulnerable target of substitution by its allied plant species. The present study is aimed at developing highly specific qualitative PCR and quantitative real-time PCR (qPCR) methods to authenticate and quantify C. verum in cinnamon-containing food products. The method targeted the ITS2-26S rRNA region of C. verum, demonstrating acceptable performance criteria and a sensitivity down to 1.24 ng. Moreover, the qPCR method was developed employing binary sample mixtures, spanning the linear dynamic range (100 to 1%, w/w) of C. verum in an adulterant species (C. cassia). The trueness (− 8.67 to − 20.69%) of the quantitative approach was effectively evaluated using blind sample mixtures. The developed method was applied to analyze 10 commercial cinnamon products, which reflected the practice of both complete and partial substitution of the higher-cost C. verum with its related, lower-cost plant species. In conclusion, the established method with specificity could not only detect but also quantify C. verum products, thus providing an accurate and powerful tool for the authentication of cinnamon-containing foods. [ABSTRACT FROM AUTHOR]

Refractive index (n) and density (ρ) are important physical parameters which are highly susceptible to the solution chemistry of liquids and their binary mixtures. The refractive index (n) and density (ρ) data of pure liquids are readily available in the literature, but the mixture data are often scarce. Therefore, in the present study, measurements of the refractive index (n) and density (ρ) of binary mixtures of n-hexanol (n-HxOH) with N,N-dimethylformamide (DMF) were performed over the composition range of 0–1 at a fixed temperature of 313.15 K. The volumetric and refractive parameters of binary mixtures were calculated using experimentally measured values of the density and refractive index. The excess parameters were evaluated and fitted to the Redlich–Kister (RK) polynomial to estimate the binary coefficients and the standard deviations. The variations in these parameters are discussed in light of molecular interactions in the mixture species. Their conformational study is supported by Fourier transform infrared (FTIR) spectroscopy. The refractive index (n) of the binary mixtures is predicted using the Lorentz–Lorentz (L–L), Weiner (Wi), Eyring–John (E–J), Gladstone–Dale (G–D), Arago–Biot (A–B), Newton (Nw), Oster (Ost), and Eykman (Eyk) mixture models. A comparison of various mixture models with experimental values of refractive indices is conducted, expressed in terms of average percentage deviation. [ABSTRACT FROM AUTHOR]

Diffusion of hydrocarbon species in an MFI‐type zeolite was investigated using a coarse‐grained approach combined with Kinetic Monte Carlo (KMC) simulations. The model was employed to capture and isolate the essential characteristics of hydrocarbon diffusion such as molecular pushing, passing, and blocking. A modified Lennard‐Jones type forcefield was used to approximate interactions between molecules, and molecules with the oxygen in the zeolite lattice. The basis for the rate expressions is configurational diffusion theory, which has been adjusted to account for an accurate representation of the motions of hydrocarbon molecules trapped in the zeolite. Diffusion coefficients were estimated for low and high loading of single hydrocarbons as well as binary mixtures. In all cases studied, reasonable agreement was achieved with reported experimental data and molecular dynamics simulations. The model is conceptualized as an analytical tool that may be used to address key engineering topics such as applications of zeolites as size‐selective barriers. [ABSTRACT FROM AUTHOR]

BACKGROUND: The highland barley, Hordeum vulgare L., is a staple food crop with superior nutritional functions in Xizang, China. It is often damaged by the black cutworm, Agrotis ipsilon (Hufnagel), which is an underground pest and difficult to effectively manage. To introduce a novel insecticide with unique mode of action, broflanilide (BFL) and its binary mixtures with chlorantraniliprole (CAP), fluxametamide, β‐cypermethrin or imidacloprid were screened out as seed treatment to control black cutworm in highland barley in the present study. RESULTS: In the laboratory bioassays, BFL had outstanding insecticidal activity to black cutworm with a median lethal dose (LD50) of 0.07 mg kg−1. The mixture of BFL × CAP at the concentration ratio of 7:40 exhibited the highest synergistic effect with a co‐toxicity coefficient of 280.48. In the greenhouse pot experiments, BFL and BFL × CAP seed treatments at 8 g a.i. kg−1 seed could effectively control black cutworm, with a low percentage of injured seedlings <20% and high control efficacies of 93.33–100% during a period of 3–12 days after seed emergence. Moreover, BFL and BFL × CAP seed treatments could promote the seed germination and seedling growth of highland barley at the tested temperatures of 15, 20 and 25 °C. CONCLUSION: Our results indicated that BFL and BFL × CAP were effective and promising insecticides as seed treatment to control black cutworm in highland barley. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Leveraging the anisotropic shape of DNA-functionalized nanoparticles holds potential for shape-directed crystallization of a wide collection of superlattice structures. Using coarse-grained molecular dynamics simulations, we study the self-assembly of a binary mixture of cubic gold nanoparticles, which are functionalized by complementary DNA strands. We observe the spontaneous self-assembly of simple cubic (SC), plastic body-centered tetragonal (pBCT), and compositionally disordered plastic body-centered tetragonal (d-pBCT) phases due to hybridization of the DNA strands. We systematically investigate the effect of length, grafting density, as well as rigidity of the DNA strands on the self-assembly behavior of cubic nanoparticles. We measure the potential of mean force between DNA-functionalized nanocubes for varying rigidity of the DNA strands and DNA lengths. Using free-energy calculations, we find that longer and flexible DNA strands can lead to a phase transformation from SC to the pBCT phase due to a gain in entropy arising from the orientational degrees of freedom of the nanocubes in the pBCT phase. Our results may serve as a guide for self-assembly experiments on DNA-functionalized cubic nanoparticles. [ABSTRACT FROM AUTHOR]

Newton's third law, action = reaction, is a foundational statement of classical mechanics. However, in natural and living systems, this law appears to be routinely violated for constituents interacting in a nonequilibrium environment. Here, we use computer simulations to explore the macroscopic phase behavior implications of breaking microscopic interaction reciprocity for a simple model system. We consider a binary mixture of attractive particles and introduce a parameter that is a continuous measure of the degree to which interaction reciprocity is broken. In the reciprocal limit, the species are indistinguishable, and the system phase separates into domains with distinct densities and identical compositions. Increasing nonreciprocity is found to drive the system to explore a rich assortment of phases, including phases with strong composition asymmetries and three-phase coexistence. Many of the states induced by these forces, including traveling crystals and liquids, have no equilibrium analogs. By mapping the complete phase diagram for this model system and characterizing these unique phases, our findings offer a concrete path forward toward understanding how nonreciprocity shapes the structures found in living systems and how this might be leveraged in the design of synthetic materials. [ABSTRACT FROM AUTHOR]

The physical mechanisms governing molecular mobility in liquids remain unresolved. Whether distinct mechanisms govern mobility in the Arrhenian and super-cooled regions, and whether the mobility in these regions can be unified remain open questions. Here, molecular dynamics simulations were used to search for a structural property with a temperature dependence related by a simple functional form to the temperature dependent translational diffusion coefficient, Dtrans. The logarithm of Dtrans was found to be a two-parameter function of F 2 , where F 2 is the mean squared-force per molecule. The relationship is demonstrated for all systems investigated: a three-bead model of ortho-terphenyl, an 80:20 binary mixture of Lennard-Jones spheres, and a system of Lennard-Jones dumbbells. For each system, the relationship holds for the entire range of temperatures under both constant pressure and constant density conditions. The same F 2 -based expression describes the translational diffusion coefficient in the Arrhenian, crossover, and super-Arrhenian regions. [ABSTRACT FROM AUTHOR]

Nucleation in systems with a metastable liquid–gas critical point is the prototypical example of a two-step nucleation process in which the appearance of the critical nucleus is preceded by the formation of a liquid-like density fluctuation. So far, the majority of studies on colloidal and protein crystallization have focused on one-component systems, and we are lacking a clear description of two-step nucleation processes in multicomponent systems, where critical fluctuations involve coupled density and concentration inhomogeneities. Here, we examine the nucleation process of a binary mixture of patchy particles designed to nucleate into a diamond lattice. By combining Gibbs-ensemble simulations and direct nucleation simulations over a wide range of thermodynamic conditions, we are able to pin down the role of the liquid–gas metastable phase diagram on the nucleation process. In particular, we show that the strongest enhancement of crystallization occurs at an azeotropic point with the same stoichiometric composition of the crystal. [ABSTRACT FROM AUTHOR]

We study low-salt, binary aqueous suspensions of charged colloidal spheres of size ratio Γ = 0.57, number densities below the eutectic number density nE, and number fractions of p = 1.00–0.40. The typical phase obtained by solidification from a homogeneous shear-melt is a substitutional alloy with a body centered cubic structure. In strictly gas-tight vials, the polycrystalline solid is stable against melting and further phase transformation for extended times. For comparison, we also prepare the same samples by slow, mechanically undisturbed deionization in commercial slit cells. These cells feature a complex but well reproducible sequence of global and local gradients in salt concentration, number density, and composition as induced by successive deionization, phoretic transport, and differential settling of the components, respectively. Moreover, they provide an extended bottom surface suitable for heterogeneous nucleation of the β-phase. We give a detailed qualitative characterization of the crystallization processes using imaging and optical microscopy. By contrast to the bulk samples, the initial alloy formation is not volume-filling, and we now observe also α- and β-phases with low solubility of the odd component. In addition to the initial homogeneous nucleation route, the interplay of gradients opens various further crystallization and transformation pathways leading to a great diversity of microstructures. Upon a subsequent increase in salt concentration, the crystals melt again. Wall-based, pebble-shaped β-phase crystals and facetted α-crystals melt last. Our observations suggest that the substitutional alloys formed in bulk experiments by homogeneous nucleation and subsequent growth are mechanically stable in the absence of solid–fluid interfaces but thermodynamically metastable. [ABSTRACT FROM AUTHOR]

The present work contributes to the development of the shadowgraph method for its routine application for an accurate determination of the Fick diffusion coefficient D11 of binary fluid mixtures. In this context, measurement and data evaluation strategies for thermodiffusion experiments where confinement and advection are potentially present are elaborated by studying two binary liquid mixtures with positive and negative Soret coefficients, i.e., 1,2,3,4-tetrahydronaphthalene/n-dodecane and acetone/cyclohexane. For obtaining accurate D11 data, the dynamics of non-equilibrium fluctuations in concentration is analyzed considering recent theory by data evaluation procedures that are demonstrated to be suitable for different experimental configurations. [ABSTRACT FROM AUTHOR]

Background: The proposed research study introduces independent concentration extraction (ICE) as a novel UV–Vis spectrophotometric approach. The approach can be used for extracting the concentration of two analytes with severely overlapped spectra from their binary mixtures. ICE is based on spectral extraction platform involving simple smart successive methods that can directly extract the original zero order spectra of the analytes at their characteristic (λmax). Chlorpheniramine maleate (CPM) and Levocloperastine fendizoate (LCF) are two commonly co-formulated drugs in cough preparations. The combined mixture was used to confirm the validity of the developed ICE tool. Another less green HPTLC was developed for the first time to separate both drugs and help also in confirming the proposed tool. Methods: For the simultaneous determination of CPM and LCF, two ecologically friendly techniques were employed. The first approach encompasses the use of the ICE spectrophotometric method that could be successively applied for extracting the concentration of two analytes with severely overlapped unresolved spectra in their binary mixtures. Other complementary methods aiming at original spectral extraction; including spectrum subtraction (SS) and unity subtraction (US) were also successfully employed to resolve the zero order spectra of the combined drugs with all their characteristic features and peaks. The second technique used, a high-performance TLC-densitometric one, was performed on silica plates with silica plates F254 and a mobile phase with a ratio of 3:3:3:1 by volume of toluene, ethanol, acetone, and ammonia as a developing system at 230 nm. Results: The presented extraction approach was executed without any optimization steps or sample pretreatment for the simultaneous determination of CPM and LCF. The method was found to be valid for their determination within concentration range of 3.0–30.0 μg mL−1 for both drugs. For HPTLC method, the resulting Rf values of CPM and LCF were 0.37 and 0.78, within concentration ranges of 0.3–4.0 μg/spot and 0.8–10.0 μg/spot, respectively. Greenness assessment of both developed methodologies showed that the HPTLC method is less green than the spectrophotometric method, yet with comparable sustainability when it comes to the used technique. Conclusion: The procedures were found to be selective, accurate, and precise for analysis of the studied binary mixture. Furthermore, the environmental impact of the introduced methods was assessed using novel greenness metrics, namely AGREE and Green Analytical Procedure Index (GAPI) to prove their ecological safety. In addition, white analytical chemistry (WAC) evaluation metric was employed to ensure the synergy and coherence of analytical, practical, and ecological attributes. [ABSTRACT FROM AUTHOR]

To recharge lithium‐ion batteries quickly and safely while avoiding capacity loss and safety risks, a novel electrode design that minimizes cell polarization at a higher current is highly desired. This work presents a dual‐layer electrode (DLE) technology via sequential coating of two different anode materials to minimize the overall electrode resistance upon fast charging. Electrochemical impedance spectroscopy and distribution of relaxation times analysis revealed the dynamic evolution of electrode impedances in synthetic graphite (SG) upon a change in the state of charge (SOC), whereas the natural graphite (NG) maintains its original impedance regardless of SOC variation. This disparity dictates the sequence of the NG and SG coating layers within the DLE, considering the temporal SOC gradient developed upon fast charging. Simulation and experimental results suggest that DLE positioning NG and SG on the top (second‐layer) and bottom (first‐layer), respectively, can effectively reduce the overall resistance at a 4 C‐rate (15‐min charging), demonstrating two times higher capacity retention (61.0%) over 200 cycles than its counterpart with reversal sequential coating, and is higher than single‐layer electrodes using NG or NG/SG binary mixtures. Hence, this study can guide the combinatorial sequence for multi‐layer coating of various active materials for a lower‐resistivity, thick‐electrode design. [ABSTRACT FROM AUTHOR]

Deep eutectic solvents (DES) represent a promising class of green solvents, offering particular utility in the extraction and development of new formulations of natural compounds such as ferulic acid (FA). The experimental phase of the study undertook a systematic investigation of the solubility of FA in DES, comprising choline chloride or betaine as hydrogen bond acceptors and six different polyols as hydrogen bond donors. The results demonstrated that solvents based on choline chloride were more effective than those based on betaine. The optimal ratio of hydrogen bond acceptors to donors was found to be 1:2 molar. The addition of water to the DES resulted in a notable enhancement in the solubility of FA. Among the polyols tested, triethylene glycol was the most effective. Hence, DES composed of choline chloride and triethylene glycol (TEG) (1:2) with added water in a 0.3 molar ration is suggested as an efficient alternative to traditional organic solvents like DMSO. In the second part of this report, the affinities of FA in saturated solutions were computed for solute-solute and all solute-solvent pairs. It was found that self-association of FA leads to a cyclic structure of the C 2 8 type, common among carboxylic acids, which is the strongest type of FA affinity. On the other hand, among all hetero-molecular bi-complexes, the most stable is the FA-TEG pair, which is an interesting congruency with the high solubility of FA in TEG containing liquids. Finally, this work combined COSMO-RS modeling with machine learning for the development of a model predicting ferulic acid solubility in a wide range of solvents, including not only DES but also classical neat and binary mixtures. A machine learning protocol developed a highly accurate model for predicting FA solubility, significantly outperforming the COSMO-RS approach. Based on the obtained results, it is recommended to use the support vector regressor (SVR) for screening new dissolution media as it is not only accurate but also has sound generalization to new systems. [ABSTRACT FROM AUTHOR]

In the present study, bio-based polymeric blends have been prepared for applications in the field of sustainable food packaging, starting from two furan-based homopolymers, poly(hexamethylene 2,5-furanoate) (PHF) and poly(pentamethylene 2,5-furanoate) (PPeF). PHF and PPeF were synthesized by two-step melt polycondensation—a solvent-free synthetic strategy—and then binary physical mixtures, PHF/PPeF, with different weight compositions were prepared by dissolution in a common solvent. The blends were processed into compression-moulded films, and molecular, morphological, structural, thermal, and mechanical characterizations were subsequently carried out. Blending did not negatively affect the thermal stability of the parent homopolymers, and good compatibility between them was observed. This strategy also allowed for the modulation of the chain rigidity as well as of the crystallinity, simply by acting on the relative weight amount of the homopolymers. From a mechanical point of view, the presence of PPeF led to a reduction in stiffness and an increase in the elongation at break, obtaining materials with an elastomeric behaviour. Evaluation of the gas barrier properties confirmed that the good barrier properties of PHF were preserved by blending. Finally, lab-scale composting tests confirmed a greater weight loss of the mixtures with respect to the PHF homopolymer. [ABSTRACT FROM AUTHOR]

This document is a summary of a special issue titled "Macroscopic and Microscopic Thermodynamics: From Fundamentals to Present Applications, 2nd Edition." It explores the broad field of thermodynamics and its applications in various scientific disciplines. The article discusses the historical development of thermodynamics and its expansion into fields such as cosmology, information science, and social sciences. It also highlights the importance of molecular thermodynamics in chemical engineering and the use of computational methods in solving thermodynamic problems. The document provides a list of the contributions included in the special issue, which cover topics such as vapor-liquid equilibrium, clathrate hydrates, binary mixtures, and surface tension. The authors emphasize the importance of thermodynamics in addressing theoretical and practical problems and highlight its potential for further research in fields like process engineering, human health, and environmental preservation. [Extracted from the article]

Clay–gravel mixture is an increasingly popular material used in geotechnical engineering for its engineering adaptability and easy accessibility. Among various granulometric factors, gravel content plays a critical role in the alteration of mixture microstructure. Its influence on mechanical behavior has been comprehensively investigated, yet the hydraulic models accounting for the paired impact of clay and gravel particles are seldomly discussed. In an effort to enhance the permeability prediction capability of this soil, a generalized binary model derived from a theoretical hydraulic conductivity expression is proposed, with the participation of two fundamental compound seepage models. High accuracy between test and calculation results indicates the reliability of this model, as well as its supremacy over conventional models. The parameter sensitivity analysis demonstrates that the proposed model, being of convincing parametric stability regardless of variant particle size distribution characteristics, has the potential to be applicable to a wide range of engineering-adapted CGMs. The predictive formula for cohesive fraction and the anomaly coefficient, as is integrated into the binary model, are explicitly discussed. Suitable for clay–gravel materials under a transitional soil state for engineering applications, this model provides a quantitative and reasonable evaluation of hydraulic conductivity with high practicality. The above findings might work as a perspective for the credible assessment of structure seepage safety behavior, as well as a quantitative evaluation method regarding the mixing quality of CGMs. [ABSTRACT FROM AUTHOR]

Due to the multiple influences of unique physicochemical properties of helium, petrographic characteristics and temperature and pressure conditions, little is known about the helium adsorption behaviors in minerals and rocks at geological conditions. Based on the grand canonical Monte Carlo simulations, this study revealed the adsorption characteristics of pure helium and the competitive adsorption of binary mixtures with different proportions of methane and helium under geological temperature and pressure conditions in quartz slit model. Molecular simulation of pure helium shows that physical adsorption of helium exists in mineral surfaces, which indicates a preservation mechanism of helium in helium source rocks. Binary mixtures simulations indicate that the adsorption capacity of methane in quartz is stronger than that of helium, and the competitive adsorption of methane increases with decreasing burial depth. This means that during the upwards migration processes of natural gas, the adsorbed helium that distributed in the migration pathway will be gradually displaced by methane, then concentrate in the hydrocarbon gases and subsequently accumulate together in favorable traps to form helium-rich natural gas reservoirs. Our results provide a molecular-scale insight into the preservation and accumulation of helium in helium source rocks and are significant for assessing the helium resource potential. [ABSTRACT FROM AUTHOR]

Using smart or low salinity waters known as green processes gained increasing attention due to their unique features and their positive impacts on the environment. In light of this fact and since there is limited knowledge about the effects of salts under engineered concentrations or binary mixtures and crude oil fractions on the interfacial tension (IFT) reduction and wettability alteration of the resinous (RSO) and asphaltenic synthetic oil (ASO), the current investigation is designed and performed for the first time. Moreover, the dynamic behavior of the IFT variation was carefully investigated and the relaxation time was obtained and modeled to see the impact of mono and divalent salts individually and in binary conditions. The relaxation times revealed that the lowest adsorption times were obtained for NaCl/CaCl2 brine regardless of the examined oil types of ASO and RSO due to the high movement affinity of the polar functional groups toward the interface consequently reducing the required time for coverage and packing of active agents at the interface. Finally, the measured contact angle values revealed a significant effect of binary salts on the wettability alteration toward strongly water-wet conditions, especially for the RSO and ASO compared with crude oil. [ABSTRACT FROM AUTHOR]

The list of standard abbreviations for JDS is available at adsa.org/jds-abbreviations-24. Nonstandard abbreviations are available in the Notes. The objective of this study was to examine the sensory interactions between lactones and ketones in a Cheddar simulation matrix through perceptual interaction analysis. The olfactory thresholds of 6 key lactones had values ranging from 8.32 to 58.88 μg/kg, whereas those of the 4 key ketones ranged from 6.61 to 660.69 μg/kg. Both Feller's additive model and σ-τ plots demonstrated complex interactions in 24 binary mixtures composed of the 6 lactones and 4 ketones, including synergy, addition, and masking effects. Specifically, we found that 6 binary mixtures exhibited aroma synergistic effects using both methods. Moreover, the σ-τ plot showed a synergistic effect of aroma in 3 ternary mixtures. The U -model further confirmed the synergistic effects of the 6 groups of binary systems and 3 groups of ternary systems on aroma at actual cheese concentrations. In an aroma addition experiment, the combination of δ-octalactone and diacetyl in binary mixtures had the most pronounced effect on enhancing milk flavor. In ternary mixtures, 2 combinations, namely δ-octalactone/δ-dodecalactone/diacetyl and γ-dodecalactone/δ-dodecalactone/acetoin, significantly enhanced the milky and sweet aroma properties of cheese, while also enhancing the overall acceptability of the cheese aroma. [Display omitted] [ABSTRACT FROM AUTHOR]

The aqueous solution of binary mixtures of amphiphilic copolymers is a potential platform for fabricating mixed polymeric micelles for pharmaceutical applications, particularly in developing drug delivery depots for a poorly water-soluble compound. This study fabricated and investigated binary mixtures of poloxamer 403 (P403) and poloxamer 407 (P407) at varying P403:P407 molar ratios to develop a vehicle for the poorly water-soluble compound, using ibuprofen as a model drug. The cooperative formation of mixed micelles was obtained, and the solubility of ibuprofen in the binary mixtures was enhanced compared to the solubility in pure water and an aqueous single P407 solution. The binary mixture with the P403:P407 molar ratio of 0.75:0.25 at a total polymer concentration of 19% w/v exhibited the temperature dependence of micellization and sol-to-gel characteristics of the thermosensitive mixed micellar gels. It possessed suitable micellization and gelation characteristics for in situ gelling systems. The release of ibuprofen from the thermosensitive mixed micellar depots was sustained through a diffusion-controlled mechanism. The findings can aid in formulating binary mixtures of P403 and P407 to achieve the desired properties of mixed micelles and micellar gels. [ABSTRACT FROM AUTHOR]

This study employs a combined experimental and theoretical approach to investigate the thermophysical properties of eucalyptol (EC) blended with a series of 1-alkanols (ranging from 1-hexanol to 1-nonanol) across a temperature spectrum of 293.15–323.15 K. Density Functional Theory (DFT) calculations at the M05-2x/6-31g(d,p) level of theory are used to optimize the geometry of EC + 1-alkanols and provide insights into the hydrogen bonding interactions between the molecules. The DFT results reveal the significance of alkyl chain length in 1-alkanols on the hydrogen bonding with EC, which is supported by the analysis of geometrical, topological properties, vibrational frequency, NMR, and molecular orbital analysis. The theoretical findings are complemented by experimental measurements of density and viscosity, which show negative deviations from ideality in excess molar volume and viscosity. This study highlights the power of DFT methods in elucidating the molecular-level interactions governing the thermophysical properties of complex binary systems. Furthermore, the DFT results provide a molecular-level understanding of the observed thermophysical behavior, allowing for the development of more accurate predictive models. The integration of experimental and theoretical approaches in this study demonstrates a powerful framework for investigating the properties of complex mixtures. [ABSTRACT FROM AUTHOR]

In this study, we present an operator splitting method (OSM) for the Cahn–Hilliard (CH) equation on a nonuniform mesh. The CH equation is a fourth-order partial differential equation that models phase separation phenomena in binary mixtures. Because the CH equation is applied in various scientific fields, numerous numerical methods have been developed to enhance the computational efficiency and accuracy. In this work, we consider a nonuniform mesh to improve spatial efficiency. To solve the CH equation in two-dimensional (2D) space on a nonuniform mesh, we consider the linear stabilized splitting (LSS) scheme along with the OSM. The LSS scheme is an unconditionally energy gradient stable method. To construct a simple numerical scheme, we consider the OSM in two-dimensional space. We validate that the proposed scheme satisfies the mass-preserving property. Furthermore, we conduct numerical experiments to demonstrate the efficiency and various properties of the proposed scheme. [ABSTRACT FROM AUTHOR]

BACKGROUND: Solid fats are critical to obtaining a wide range of food texture and quality characteristics, but their consumption is strongly associated with higher cardiovascular disease risks. Structuring unsaturated oils with natural waxes into oleogels (OG) is an innovative solution to develop fat mimics with a healthier profile. RESULTS: Soy wax (SW), beeswax (BW) and carnauba wax (CW), have been used in binary mixtures of waxes, aiming to understand their interactions and influence on OG quality properties and microstructural characteristics. In the present study, OGs were produced using binary wax mixtures and analyzed for texture, color, smoke point, microstructure, Fourier‐transform infrared spectroscopy (FTIR) and X‐ray diffraction (XRD). Wax combinations led to antagonistic (mixtures with SW) and synergistic interactions (BW/CW) based on their mechanical properties. At the microstructural level BW/CW blends showed a reduction in crystal size and with a more compact structure. XRD and FTIR spectra revealed a packing of orthorhombic perpendicular subcell for most OGs, whereas SW produced samples with an arrangement with β' crystals, characteristic of edible solid fats. Additionally, when compared to commercial beef fat, BW/CW mixtures showed similar quality attributes indicating that they could act as fat mimic. CONCLUSION: The combined analysis of microstructure, spectroscopic and mechanical properties enhanced the understanding of how the nature of the interactions between waxes and lipid phases impact in the final quality of the structured oils. The study's insights indicate that binary wax combinations can efficiently replace solid fats, offering healthier alternatives at the same time as preserving desired sensory characteristics. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

It is acknowledged that injecting CO2 into oil reservoirs and saline aquifers for storage is a practical and affordable method for CO2 sequestration. Most CO2 produced from industrial exhaust contains impurity gases such as H2S that might impact CO2 sequestration due to competitive adsorption. This study makes a commendable effort to explore the adsorption behavior of CO2/H2S mixtures in calcite slit nanopores. Grand Canonical Monte Carlo (GCMC) simulation is employed to reveal the adsorption of CO2, H2S as well as their binary mixtures in calcite nanopores. Results show that the increase in pressure and temperature can promote and inhibit the adsorption capacity of CO2 and H2S in calcite nanopores, respectively. CO2 exhibits stronger adsorption on calcite surface than H2S. Electrostatic energy plays the dominating role in the adsorption behavior. Electrostatic energy accounts for 97.11% of the CO2-calcite interaction energy and 56.33% of the H2S-calcite interaction energy at 10 MPa and 323.15K. The presence of H2S inhibits the CO2 adsorption in calcite nanopores due to competitive adsorption, and a higher mole fraction of H2S leads to less CO2 adsorption. The quantity of CO2 adsorbed is lessened by approximately 33% when the mole fraction of H2S reaches 0.25. CO2 molecules preferentially occupy the regions near the pore wall and H2S molecules tend to reside at the center of nanopore even when the molar ratio of CO2 is low, indicating that CO2 has an adsorption priority on the calcite surface over H2S. In addition, moisture can weaken the adsorption of both CO2 and H2S, while CO2 is more affected. More interestingly, we find that pure CO2 is more suitable to be sequestrated in the shallower formations, i.e., 500–1500m, whereas CO2 with H2S impurity should be settled in the deeper reservoirs. [ABSTRACT FROM AUTHOR]

Separation of equally sized particles distinguished solely by material properties remains still a very challenging task. Here a simple separation of differently charged, thermo‐responsive polymeric particles (for example microgels) but equal in size, via the combination of pressure‐driven microfluidic flow and precise temperature control is proposed. The separation principle relies on forcing thermo‐responsive microgels to undergo the volume phase transition during heating and therefore changing its size and correspondingly the change in drift along a pressure driven shear flow. Different thermo‐responsive particle types such as different grades of ionizable groups inside the polymer matrix have different temperature regions of volume phase transition temperature (VPTT). This enables selective control of collapsed versus swollen microgels, and accordingly, this physical principle provides a simple method for fractioning a binary mixture with at least one thermo‐responsive particle, which is achieved by elution times in the sense of particle chromatography. The concepts are visualized in experimental studies, with an intend to improve the purification strategy of the broad distribution of charged microgels into fractioning to more narrow distribution microgels distinguished solely by slight differences in net charge. [ABSTRACT FROM AUTHOR]

A more focused scientific approach in the context of a mixture of thermoelastic solids would entail investigating the basic ideas guiding the behavior of the complex materials, including constitutive model development, multi-scale modeling at various length scales, and design optimization for thermoelastic solids with their precise properties. The present work is set up to study the effect of the magnetic field as an external effect on the mixture of two interacting thermoelastic solids. The fundamental mathematical equations were shown and solved by the analytical harmonic wave solution to give the solution of the descriptive functions of the discussed problem. The displacements and stresses for the mixture of the two interreacted thermoelastic solids with the mutual temperature were clarified in the 2-D and 3-D. The results are analyzed and discussed. The obtained solution for the functions is finite everywhere. The solutions for the quantities of practical interest are represented graphically with different choices of the wave number of the harmonic wave as the magnetic field with time. In addition to the numerous physical factors in the governing field equations as depicted in the figures, boundary conditions also play a role in the current damping phenomenon. [ABSTRACT FROM AUTHOR]

Pulsating airflow-driven gas-solid fluidization is an effective method to segregate particles of different densities. The current article presents an elaborate computational study on the development of simulation methodology, and parametric trend identification of pulsating airflow-driven granular segregation for the first time using computational fluid dynamics (CFD), discrete element modeling (DEM) coupled analysis. The rigorous validation of the computational prediction has been produced against the experimental result reported by Li et al. (2021) and an excellent agreement has been observed. Segregation behavior for different density ratios of particles, different patterns of pulsation, and different particle shapes is presented in the current article. The segregation index improves with the density ratio of the binary mixture of particles, but the rate of increment of the segregation index is highly dependent on the airflow rate. Near the optimal value of airflow rate, the rate of increment of the segregation index reduces with the density ratio. Keeping the bed height and material property constant, different patterns of pulsation namely—sinusoidal, triangular, and exponential have been adopted. The segregation index is higher for sinusoidal patterns, whereas it reduces when the pattern is changed to triangular and exponential. Particles of constant volume with different shapes are also considered to understand the effect of particle shape on segregation. The segregation index deteriorates with the increasing surface area of the particle at constant volume. [ABSTRACT FROM AUTHOR]

Fodder Galega (Galega orientalis Lam.) is a perennial legume adapted to the temperate regions of the world. The objective of this research was to compare the performance of fodder Galega to alfalfa (Medicago sativa L.), sainfoin (Onobrychis viciifolia Scop.), and cicer milkvetch (Astragalus cicer L.) in monocultures and grass–legume mixtures. From 2018 to 2020, a multiple-location trial was conducted at Swift Current, Saskatoon, Melfort, SK and Beaverlodge, AB, Canada. The average forage mass of fodder Galega in monoculture was 3226, 1176, and 1678 kg·ha–1 at Melfort, Saskatoon, and Swift Current, respectively, and was lower than alfalfa. However, fodder Galega and alfalfa had similar forage mass at Beaverlodge (7900 and 7670 kg·ha−1, respectively). The proportion of fodder Galega in the grass–legume mixtures was 36%–42% in 2019, decreasing to 3%–27% at Saskatoon. At Swift Current, fodder Galega in the mixtures was 11%–13% in 2019, which almost disappeared from the stand in 2020. At Beaverlodge, fodder Galega maintained 38%–47% in 2019 and increased to 47%–69% in 2020. Fodder Galega had similar acid detergent fiber to cicer milkvetch at two of four sites, which was lower than those of alfalfa and sainfoin. The crude protein of fodder Galega and its mixtures with grasses was lower than other mixtures at the three Saskatchewan sites, but was higher at Beaverlodge. Our results indicate that fodder Galega has potential to be utilized as a forage legume in cooler northern regions, but its productivity was low in the Dark Brown and Brown soil. [ABSTRACT FROM AUTHOR]

The Cahn-Hilliard equation is a fundamental model in the study of phase separation and coarsening phenomena in binary mixtures. The paper investigates the perturbative solutions of the one-dimensional Cahn-Hilliard equation for small spatial and temporal variables. Starting with a uniform state, a small perturbation was introduced and first-order perturbation expansion was derived. Utilizing Fourier transforms, the linearized form of Cahn-Hilliard equation was solved to obtain the general solution. The dispersion relation revealed the growth rates of perturbation modes, providing insight into the early-time dynamics of phase separation. The analytical approach lays the groundwork for understanding the evolution of small perturbations and their impact on the phase separation process in binary systems. This work has potential applications in materials science, particularly in understanding the microstructural development of alloys and polymer blends. [ABSTRACT FROM AUTHOR]

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Glyphosate and 2,4-dichlorophenoxyacetic acid (2,4-D) are the most widely used pesticides in the world. In this work, the cytogenotoxic potential of these herbicides and their binary mixtures was investigated using A. cepa test. 2,4-D was assayed at 0.4 – 400 μg L−1 and glyphosate at 0.65 – 650 μg L−1 concentration range. The concentrations evaluated cover those permitted by Brazilian legislation for the protection of aquatic life and human health. Sixteen binary mixtures were examined to replicate different contamination scenarios. When analyzed separately, 2,4-D at 400 μg L−1 inhibited the mitotic index, while glyphosate at 0.65 and 65 μg L−1 increased it. In addition, the herbicides increased the frequency of chromosomal aberrations (2,4-D at 0.4, 4, and 40 μg L−1 and glyphosate at 0.65, 65, and 650 μg L−1) and micronuclei (2,4-D at 400 μg L−1 and glyphosate at 650 μg L−1). Regarding the mixtures, six of them were cytotoxic while eight were genotoxic. Additive, synergistic, or potentiated effects were observed. However, none of the mixtures tested increased the frequency of micronuclei. The results showed that even concentrations allowed by Brazilian legislation pose a potential risk to exposed organisms. There is little research on the cytogenotoxic effects of 2,4-D + glyphosate mixtures, so this is the first study to analyze a large number of combinations. The detection of additive, synergistic, or potentiated toxicities highlights the need for better pesticide legislation and discussions among regulators and environmental managers regarding pesticide mixtures in water. [ABSTRACT FROM AUTHOR]