Search Results (262)

The intense demand for alternatives to conventional plastics has increasingly motivated the development of biodegradable packaging. However, the ecological impact of these materials when discarded in natural settings has not yet been evaluated. Therefore, this study investigated the effects of films based on chia mucilage in different aquatic environments. The solubilization time varied according to water type, ranging from 40 min in ultrapure, deionized, and distilled water to 230 min in saline water. After solubilization, all water samples exhibited increased turbidity (from 1.04 to 15.73 NTU in deionized water) and apparent color (from 0 to 44 PCU in deionized water) as well as pH variations depending on ionic strength. Deionized water also showed the highest viscosity increase (>350 Pa·s at 1 s⁻¹). UV–Vis spectra revealed a moderate rise in absorbance between 236 and 260 nm, indicating organic compound release. Regarding phytotoxicity, the solubilized films had no toxic effect and promoted a biostimulating effect on root elongation, with Relative Germination Index values exceeding 140% in most samples. These results reinforce the potential of chia-based films for controlled disposal, particularly in low-salinity environments, while highlighting the importance of evaluating post-solubilization interactions with aquatic systems. Full article

The interactions of Fe³⁺ with some ligands (Tranexamic (TXA⁻), Indole-3-acetic (IAA⁻), and Aminomethylphosphonic (AMPA²⁻) acids) of biological and environmental interest were studied. The speciation studies were performed in NaNO_3(aq) and NaCl_(aq) using potentiometric and, only for IAA⁻, spectrophotometric titrations at T = 298.15 K and 0.01 ≤ I/mol dm⁻³ ≤ 1.0. The proposed speciation models are as follows: Fe(TXA)H³⁺, Fe(TXA)₂⁺, Fe(TXA)(OH)⁺, and Fe(TXA)(OH)_2(aq) for TXA⁻; Fe(IAA)²⁺ for IAA⁻; and Fe(AMPA)H₂³⁺, Fe(AMPA)H²⁺, and Fe(AMPA)⁺ for AMPA²⁻. A comparison of logβ for the common FeL species gives logβ_FeIAA = 6.56 and logβ_FeAMPA = 14.84 (at I = 1.00 mol dm⁻³ and T = 298.15 K), suggesting that AMPA²⁻ has a higher complexing ability towards Fe³⁺ than IAA⁻. The dependence on the ionic strength of the formation constants was modeled by means of a Debye–Hückel type equation and the SIT model, whilst the sequestering ability of the investigated ligands towards Fe³⁺ was quantified at various pHs, ionic strengths, and in the different supporting electrolytes by means of an empirical pL_0.5 parameter. To complete this study of the behavior of the different Fe³⁺/ligand systems, various simulations in biological fluids and natural waters were conducted. Full article

Six activated carbons from tomato (Solanum lycopersicum L.) stems (TS-AC) were synthesized by carbonization and chemical activation using potassium hydroxide (KOH) and sodium hydroxide (NaOH) at temperatures of 550, 650, and 750 °C. These TS-ACs were then evaluated as adsorbents to remove 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chlorophenoxyacetic acid (MCPA) from aqueous solutions. The adsorption kinetics of both herbicides followed the pseudo-second-order model, closely correlating with the mesopore volume of the TS-AC. The Langmuir isotherm accurately described the adsorption process for both 2,4-D and MCPA. The porous structure of TS-AC, characterized by micropore volume and specific surface area, significantly influenced the maximum adsorption capacities. The adsorption of both herbicides was pH dependent, but ionic strength had no significant effect. Regeneration testing, conducted over three cycles, showed less than a 15% reduction in herbicide adsorption capacity. This study demonstrates that agricultural waste, specifically tomato stems, can be effectively valorized by using simple activation techniques in TS-AC that are efficient adsorbents to remove organic pollutants, such as herbicides, from aqueous media. Full article

This work focuses on the stability analysis of water-in-oil macroemulsions with a crude oil from the Sacha Field in Ecuador. This field is an important hydrocarbon resource in Ecuador with a typical bottom freshwater drive. The comprehensive stability analysis includes coalescence, water resolution or phase separation, and water–oil interfacial tension and interfacial dilatational viscoelastic modulus measurements over time. Two main parameters, due to their relevance, were controlled in these experiments: water salinity and temperature. The analysis reported here is the first focused on this important resource in Ecuador. Findings shed light on which mechanisms more likely control the stability of these water-in-oil macroemulsions. Results herein suggest that regardless of temperature, low-salinity water favors emulsion stability, likely due to the tendency of a stiffer interface formation at low-ionic strength, as interfacial viscoelasticity measurements show. This implies that the low-ionic strength water from the aquifer can enable the formation of stable emulsions. In contrast, water resolution depends significantly on temperature, possibly due to higher sedimentation rates. The implication is that if emulsions do not break up before cooling off, the emulsion can become more stable. Finally, analysis of the interface buildup rates could explain the observed increase in emulsion stability over time. Full article

Cu matrix composites, because of their high mechanical strength, are often used as conductors in high-performance electrical applications. These composites are manufactured through thermomechanical processing, which introduces a high density of particles that act as obstacles to dislocation motion. Increasing the density of these particles enhances the mechanical strength of the conductors, which we tested under static loading. Under cyclic loading, especially pulsed electrical mechanical loading, conductors may soften, harden, or even fail. Failure is likely to occur whenever the applied stress exceeds the flow stress of the conductors. Understanding and predicting the performance of conductors under cyclic loading can help researchers estimate the lifespan of any apparatus made from these conductors. The performance of conductors depends on whether the strengthening particles are characterized by ionic interatomic bonding or metallic bonding. During fabrication, we observed both the accumulation of dislocations and the dissolution of particles (which added more solute atoms to the matrix). Because both dislocations and solute atoms tend to migrate at room temperature or higher, the complexity of microstructure changes increases in composites under cyclic loading. To minimize such complexity, we designed our test to determine fatigue properties at 77 K. We subjected the conductors to cyclic fatigue tests using a load-controlled mode (the mode most commonly used in applications). This work sheds light on the correlation between tensile properties and fatigue properties in our composite conductors. We found that the correlation varied, depending on whether the conductors had been strengthened by ionic bond or metallic bond particles. Full article

The co-occurrence of microplastics (MPs) and antibiotics as emerging contaminants demonstrates significant ecological perturbations in soil matrices. Of particular scientific interest is the potential for MPs to mediate the environmental fate and transport dynamics of co-existing antibiotics. This study investigated MP-mediated ciprofloxacin (CIP) adsorption in lateritic soils. Batch experiments with polyethylene (PE), polypropylene (PP), and poly (ethylene-terephthalate) (PET) revealed soil components dominated CIP retention, while 10% (w/w) MPs reduced soil adsorption capacity by ≥10.8%, with inhibition intensity following PET > PE > PP. Adsorption thermodynamics exhibited significant pH dependence, achieving maximum sorption efficiency at pH 5.0 (± 0.2), which was approximately 83%. Competitive adsorption analysis demonstrated inverse proportionality between ionic strength and CIP retention, with trivalent cations exhibiting superior competitive displacement capacity compared to mono- and divalent counterparts. Isothermal modeling revealed multilayer adsorption mechanisms governed by hybrid chemisorption/physisorption processes in both soil and MP substrates. Spectroscopic characterization suggested differential adsorption pathways: MP-CIP interactions were primarily mediated through hydrophobic partitioning and π-π electron coupling, while soil–MP composite systems exhibited dominant cation exchange capacity and surface complexation mechanisms. Notably, electrostatic attraction/repulsion forces modulated adsorption efficiency across all experimental conditions, particularly under varying pH regimes. This work advances understanding of co-contaminant dynamics in soil ecosystems, informing risk assessment frameworks. Full article

This study presents a detailed thermodynamic investigation on the protonation behavior of tartronic acid in aqueous solutions of various ionic media, including sodium chloride, potassium chloride, tetramethylammonium chloride, and tetraethylammonium iodide. Specifically, potentiometric measurements were performed at temperatures ranging from 288.15 to 310.15 K and ionic strengths between 0.1 and 1.0 mol dm⁻³ to determine stoichiometric protonation constants in different ionic media. The formation of weak complexes between tartronate and alkaline metal cations was obtained by means of the ΔpK method. Moreover, data were modeled using the Debye–Hückel equation and Specific Ion Interaction Theory (SIT), allowing for the calculation of standard thermodynamic parameters and the assessment of the dependence of protonation constants on ionic strength. Additionally, the protonation behavior of tartronic acid was compared with that of structurally related acids, such as malonic and mesoxalic acids, providing insights into the role of molecular structure in acid dissociation. The results emphasize the significant role of entropic contributions in the protonation process and provide a comprehensive model for the thermodynamic properties of tartronic acid across a wide range of experimental conditions. Full article

Chitosan is widely used in drug delivery applications, due to its biocompatibility, bio-degradability, and low toxicity. Nevertheless, its properties can be enhanced through the physical or chemical modification of its amino and hydroxyl groups. This work explores the electrostatic complexation of two chitosan samples of differing lengths with two poly(N-isopropylacrylamide) (PNIPAM) homopolymers of different molecular weight carrying a chargeable carboxyl end group. This interaction enables the electrostatic binding of PNIPAM side chains onto the chitosan backbone through the amino groups, and could be considered as an alternative grafting method. Dynamic and electrophoretic light scattering techniques were employed in order to study the solution/dispersion properties of the formed complexes as a function of the PNIPAM concentration, or, equivalently, the molar/charge ratio of the two components. The obtained results revealed that their mass, size, and charge mostly depend on the length of the two individual constituents, as well as their mixing ratio. Furthermore, their response to changes in their environment, namely temperature and ionic strength, was also examined, demonstrating the effect of either the thermoresponsiveness of PNIPAM or the electrostatic charge screening, respectively. Fluorescence spectroscopy, utilizing pyrene as a probe, provided information regarding the hydrophobicity of the formed complexes, while images from scanning transmission electron and atomic force microscopies further elucidated their morphology, which was found to be closely related to that of the corresponding chitosan molecule. Finally, their potential as drug delivery vehicles was also investigated, utilizing curcumin as a model drug at various loading concentrations. Full article

COVID-19 antibody detection is dependent on highly specialized, time-consuming techniques, such as PCR separation, DNA amplification, and other methods such as spectrophotometric absorption. For these reasons, specialized technical training is necessary because individual diagnostic treatment is difficult. We have attempted to perform rapid sensing with a detection time of only 30 s. Additionally, we used a wearable multi-layer graphene oxide nanocolloid synthetic skin tattoo probe assay for influenza and COVID-19 virus detection with an electrochemical antigen–antibody redox ionic titration circuit. Cyclic voltametric−2 V~2.0 V potential windows were used. The diagnostic detection limit was determined using stripping anodic and cathodic amplifiers, and the working probe was fabricated with a graphene molecule structure with a virus antigen-immobilized amplifier. With redox potential strength obtained within −1.0 V~−1.3 V ionic activity, anodic and cathodic current linearly increased in the phosphate-buffered saline 5 mL electrolyte. The results indicate that instant detection was enabled via individual and wearable tattoo sensors. Full article

Protolytic reactions on the surface of a titania photocatalyst (TiO₂ P25 containing chlorine impurities) were studied using potentiometric and calorimetric acid-base titration. The impurity was removed by either washing or heat treatment. The efficiency of purification was tested by chlorine (TOX) analysis and acid-base titration. Common intersection points of −0.023 and −0.021 mmol/g were obtained for the original and 400 °C heat-treated samples, which are in good agreement with the measured TOX value of 28 mmol/kg. The point of zero charge of the purified sample was determined to be 6.50. Titration data were fitted to simulate protolytic reactions during isothermal calorimetric titrations of purified titania. The evolved heat was measured, and data points were corrected with the heat of mixing and neutralization. The quantity of charged surface species formed in each step of titration was calculated using the parameters from the constant capacitance model fit. The partial molar enthalpy values of the exothermic and endothermic processes of surface protonation (ΔH_pr, −17.47 to −16.10 kJ/mol) and deprotonation (ΔH_depr, 32.53 to 27.08 kJ/mol) depend slightly on the ionic strength of suspensions. The average standard enthalpy of one proton transfer reaction is −23.54 ± 1.75 kJ/mol, which is consistent with the literature. Full article

Marine polysaccharide hydrogels have emerged as an innovative platform for regulating the in vivo release of natural bioactive compounds for medical purposes. These hydrogels, which have exceptional biocompatibility, biodegradability, and high water absorption capacity, create effective matrices for encapsulating different bioactive molecules. In addition, by modifying the physical and chemical properties of marine hydrogels, including cross-linking density, swelling behavior, and response to external stimuli like pH, temperature, or ionic strength, the release profile of encapsulated bioactive compounds is strictly regulated, thus maximizing therapeutic efficacy and minimizing side effects. Finally, by using naturally sourced polysaccharides in hydrogel formulations, sustainability is promoted by reducing dependence on synthetic polymers, meeting the growing demand for eco-friendly materials. This review analyzes the interaction between marine polysaccharide hydrogels and encapsulating compounds and offers examples of how bioactive molecules can be encapsulated, released, and stabilized. Full article

Nowadays, the application of protective multicomponent coatings based on hard metal nitrides is increasingly used to increase the resistance of structures and tools to wear, corrosion, and oxidation. In the present work, the multicomponent system Ti-Al-Ta-Si-N is studied, which has high hardness and crack resistance combined with thermal stability and oxidation resistance. The process of formation of the nanocrystalline structure of the coating during its deposition on materials plays a key role in the optimization of these properties. The nanocrystalline structure of the coating is formed due to Si impurity, which is poorly soluble in the Ti_1−x−yAl_xTa_yN system based on B1-TiN and segregates mainly along grain boundaries, forming grain boundary amorphous phases of Si_zN type. In order to find the optimal composition of multicomponent coatings with improved physical and mechanical properties, it is necessary to understand the peculiarities of interaction of Si impurity with the surface of B1-TiN phase in the presence of Al and Ta substitutional impurities. In the present work, with the help of first-principles calculations of electronic and atomic structure of (001) and (111) surfaces of the Ti_1−x−yAl_xTa_yN system with adsorbed Si atom and the interatomic bond study apparatus based on the calculation of a crystal orbital Hamilton population and a crystal orbital bond index, the nature of the bonds between adsorbed Si and the N, Ti, Al, and Ta atoms of the Ti_1−x−yAl_xTa_yN surface system has been studied. It was found that the binding energy of Si with the Ti_1−x−yAl_xTa_yN surface system can be both higher and lower than the binding energy of its bonding with the surface of the binary TiN compound depending on the position of the Al and Ta substitution atoms in the surface layers. The Si bonding with the atoms of the Ti_1−x−yAl_xTa_yN surface is ionic–covalent in nature. It is shown that the Si-Ta interaction has the highest degree of covalency and strength, and the Si-Al interaction is predominantly ionic in most cases considered and is weaker than the Si-Ti and Si-N bonds. Impurity atoms of Al or Ta have very little effect on the Si-Ti and Si-N bonds due to the local nature of the bonds in the Ti_1−x−yAl_xTa_yN surface system with adsorbed silicon atoms. Full article

Chelation therapy is currently successfully applied to reduce the aluminum burden and its neurodegenerative consequences. In view of a possible application to aluminum chelation therapy, here we have studied the complexation of hydroxybenzoic acids, namely, vanillic, syringic and gallic acids, towards aluminum ion at physiologically relevant conditions as regards temperature (37 °C) and ionic strength (i.e., 0.16 M NaCl). The solubility values and the protonation constants of the hydroxybenzoic acids were primarily assessed to estimate the competition of these acids towards aluminum and H⁺ ions. Then, potentiometric titrations were carried out, and the speciation analysis indicated a pH-dependent complexation occurring at a 1:1 hydroxybenzoic acid-to-aluminum ratio for vanillic and syringic, and 1:1, 2:1 and 3:1 ligand-to-Al(III) ratios for gallic. Gallic acid forms more stable complexes with Al(III) ion than vanillic and syringic acids and could therefore represent a good candidate for being used as sequestering agents for Al(III) ion. Full article

Using the self-consistent field approach, we studied the salt-controlled vertical segregation of mixed polymer brushes immersed into a selective solvent. We considered brushes containing two types of chains: polyelectrolyte (charged) chains and neutral chains. The hydrophobicity of both types of chains is characterized by the Flory–Huggins parameters ${\chi }_C$ and ${\chi }_N$, respectively. It was assumed that the hydrophobicity is varied only for the polyelectrolyte chains (${\chi }_C$), while other polymer chains in the brush remain hydrophilic (${\chi }_N=0$) and neutral. Thus, in our model, the solvent selectivity ($\chi ={\chi }_C-{\chi }_N$) was varied, which can be controlled in a real experiment, for example, by changing the temperature. At low salt concentrations, the polyelectrolyte chains swell and occupy the surface of the mixed brush. At high salt concentrations, the hydrophobic polyelectrolyte chains collapse and give place to neutral chains on the surface. By changing the selectivity of the solvent and the ionic strength of the solution, the surface properties of such mixed brushes can be controlled. Based on the numerical simulations results, it is shown how the critical selectivity corresponding to the segregation transition in polyelectrolyte/neutral brushes depends on the ionic strength of the solution. It is shown that at the same ionic strength, the critical selectivity increases with an increasing degree of dissociation of charged groups, as well as with an increasing fraction of polyelectrolyte chains in the mixed brush. It has also been shown that at low ionic strengths, the critical selectivity of the solvent decreases with increasing grafting density, while at high ionic strengths, on the contrary, it increases. Within the framework of the mean field theory, a two-parameter model has been constructed that quantitatively describes these dependencies. Full article

A multi-analytical approach was used to comprehensively characterize the acid-base, thermal, and surface properties of agri-food processing wastes (i.e., original and pre-treated bergamot, grape and olive pomaces). These biomasses, often underutilised and inadequately studied in terms of their physicochemical properties, were investigated under varying ionic strength conditions at t = 25 °C. This investigation uniquely integrates multiple advanced techniques: Brunauer–Emmett–Teller porosimetry, Scanning Electron Microscopy, Thermogravimetric Analysis coupled with Fourier Transform Infrared Spectroscopy, Differential Scanning Calorimetry, Attenuated Total Reflectance Fourier-Transform Infrared, and potentiometry to provide a holistic understanding of these biomasses potential for environmental remediation. The modelling of ionic strength-dependent acid-base behaviour, established using an extended Debye–Hückel-type equation, revealed the dominant role of carboxylic groups as active sites across all pomace types, although with variations in abundances across the different samples. Additionally, morphological analysis highlighted the presence of irregularly shaped particles, heterogeneous size distributions, and distinct thermal stability trends, with grape pomace exhibiting the highest mass loss. These findings underscore the significant potential of these biomasses for the remediation of cationic pollutants from natural waters. Moreover, this comprehensive characterisation not only advances the understanding of agri-food waste valorisation but also provides a robust framework for designing targeted strategies in environmental applications. Full article