Search Results (116)

Smectite clay minerals are known to readily form thixotropic physical gels in aqueous media, even at low volume fractions. Although the rheological properties of these gels are closely related to the microstructure of the network, the influence of the clay’s physicochemical characteristics remains insufficiently understood. In this study, we systematically investigated the relationships between particle size, cation exchange capacity, and zeta potential, and the rheological behavior of aqueous dispersions of four synthetic smectites. After thorough deionization, dispersions were prepared at controlled NaCl concentrations. We found that the zeta potential strongly correlates with the fineness of the network structure and governs macroscopic rheological responses such as viscosity, yield stress, and gelation behavior. Even under identical conditions, gel transparency and structural coarseness varied significantly among clay types. Furthermore, the storage modulus was influenced not only by network density but also by the intrinsic stiffness of the clay branches. These findings demonstrate that zeta potential serves as a unified indicator of structure and function in smectite dispersions and offer useful insights for gel design in colloidal and soft matter systems. Full article

Composite electrodeposited coatings hold significant potential for marine and aerospace applications due to their synergistic corrosion resistance and wear durability, yet nanoparticle agglomeration and interfacial incompatibility persistently undermine their performance. Conventional dispersion techniques—mechanical agitation, surfactants, or high-energy methods—fail to resolve these issues, often introducing residual stresses, organic impurities, or thermal damage to substrates. This study addresses these challenges through a novel thermal-assisted alkaline etching (TAE) protocol that synergistically removes surface oxides and enhances colloidal stability in β-SiC nanoparticles. By combining NaOH-based etching with low-temperature calcination (250 °C), the method achieves oxide-free SiC surfaces with elevated hydrophilicity and a ζ-potential of −25 mV, enabling submicron clustering (300 nm) without surfactants. Electrodeposited Co/SiC coatings incorporating TAE-SiC exhibited current-modulated reinforcement, achieving optimal SiC incorporation (5.9 at% Si) at 8 A/dm² through electrophoretic–hydraulic synergy, along with uniform cross-sectional distribution validated by SEM. Tribological assessments revealed shorter wear tracks in TAE-SiC-enhanced coatings compared to their untreated counterparts, suggesting enhanced interfacial coherence despite a comparable mass loss. Demonstrating scalability through cost-effective aqueous-phase chemistry, this methodology provides a generalized framework applicable to other ceramic-reinforced systems (e.g., Al₂O₃ and TiC), offering transformative potential for next-generation protective coatings in harsh operational environments. Full article

The drying structures of droplets of colloidal aqueous dispersions exhibit a wide variety of patterns depending on experimental conditions. It has been established by previous researchers that capillary flows and Marangoni convection significantly influence the macroscopic pattern formation. To the best of our knowledge, this study is the first to focus on sessile droplets of aqueous dispersions containing hollow particles. These hollow particles have a lower density than water and thus float in the medium. The drying pattern of these droplets was markedly different from the well-known ring pattern. Instead, a bump-shaped structure—often referred to as a “coffee-eye”—was formed due to the accumulation of particles at the center of the dried film. While a ring pattern was still present, it was extremely narrow and barely noticeable. This behavior is attributed to the dominance of the buoyant motion of the hollow particles, which prevented their transport by capillary flow. The findings of this study provide fundamental and important insights into the drying structures of various types of colloidal droplets. Full article

Wool textiles with multifunctional properties such as self-cleaning, antibacterial, electrical conductivity, UV blocking etc. have recently attracted interest. Among the materials employed towards their development, carbon nanotubes (CNTs) have been widely investigated due to their unique chemical, mechanical and electrical properties, exhibiting also notable UV-blocking properties. However, their limited dispersibility in solvents, particularly in water, has hindered their extensive industrial application and diminished their significant potential. In this work, two guanidinylated derivatives of hyperbranched polyethyleneimine (GPEI5k and PEI 25K) functionalized oxCNTs (oxCNTs@GPEI5K and oxCNTs@GPEI5K), with exceptional aqueous compatibility and colloidal stability, developed in our recent publication, were evaluated as to their antibacterial activity on Gram (-) Escherichia coli and Gram (+) Staphylococcus aureus bacteria and their cytotoxicity against mammalian cells, and the most promising, i.e., oxCNTs@GPEI5K, was subsequently used as finishing agent of wool fabric. The resulting wool textiles were evaluated for color, wash fastness, antibacterial properties, and UV-blocking performance. The GPEI-functionalized oxCNTs derivative, exhibited uniform distribution and good adhesion onto the wool fabrics yielding multifunctional wool fabrics with sustained antibacterial properties even after multiple washing cycles. Additionally, the modified textiles exhibited improved ultraviolet protection, highlighting their potential for multifunctional applications in antibacterial and UV-shielding textiles. Full article

The present work investigates the rheological behavior of ceramic slurries made of hydroxyapatite powders doped with magnesium and strontium ions and selected as particularly relevant for biomedical applications. The incorporation of doping ions into the apatite crystal structure is a well-known way to enhance the bioactivity of hydroxyapatite through compositional and structural changes, however, this also affects the rheological properties relevant to the fabrication of ceramic devices by forming techniques based on the manipulation of aqueous slurries. We analyzed the effect of different apatitic chemical compositions, powder content, and dispersant amount on the shear behavior and flowability of slurries, thus finding that the structural changes in hydroxyapatite induced by ion doping significantly affected the colloidal stability of the apatite powders and the viscoelasticity of the slurries. This leads to improved rheological behavior in the hydroxyapatite suspensions, which is suitable for the future development of ceramic slurries, particularly for achieving novel ceramic devices by extrusion-based techniques. Full article

Paint loss is one of the main forms of deterioration in historical wall paintings, generally restored by the application of chromatic reintegration. In the specific case of outdoor exposed paintings, it is essential to find a binder that will withstand diverse weather conditions. Since chromatic reintegrations have to be compatible with the original painting, fresco paint mock-ups were manufactured and compared to chromatic reintegrations made with an aqueous colloidal dispersion of silica nanoparticles as binder. The physical compatibility was studied by colour spectrophotometry and measurements of static contact angle, gloss, and roughness values, together with a peeling test, stereomicroscopy, and polarised light microscopy. They were also characterised from a mineralogical, chemical, and molecular point of view using X-ray diffraction, X-ray fluorescence and Fourier-transform infrared spectroscopy. The microtexture was studied by scanning electron microscopy with energy-dispersive X-ray spectroscopy. Chromatic reintegrations showed similar roughness and lower gloss values than frescoes, and the nano-silica binder ensured the natural breathability of the wall. Overall, the chemical nature of pigments was highly influential. The reintegrations with silicate-based pigments were more homogenous, with hardly any fissures, while those carried out with sulphide- or oxide-based pigments were severely cracked. The use of verdigris is discouraged due to the lack of affinity between the binder and the pigment. Full article

This study explored the formation of soft colloidal particles from a diblock ionomer (DI) with the monomeric composition (acrylonitrile)_x-co-(glycidyl methacrylate)_y-b-(3-sulfopropyl methacrylate potassium)_z—abbreviated as (A_xG_y)S_z, where x >> z > y. A colloidal dispersion was generated by introducing water into the pre-prepared DMSO solutions of DI, which led to micelle formation and subsequent coagulation. The assembly of the hydrophobic (A_xG_y) blocks was influenced by water content and chain conformational flexibility (the ability to adopt various forms of conformation). The resulting microgel structure (in particle form) consists of coagulated micelles characterized by discrete internal hydrophobic gel domains and continuous external hydrophilic gel layers. Characterization methods included light scattering, zeta potential analysis, and particle size distribution measurements. In contrast, the copolymer (A_xG_y) chains form random coil aggregates in DMSO–H₂O mixtures, displaying a chain packing state distinct from the hydrophobic gel domains as aforementioned. Additionally, the amphiphilic glycidyl methacrylate (G) units within the (A_xG_y) block were found to modulate the microgel dimensions. Notably, the nanoscale hydrogel corona exhibits high accessibility to reactive species in aqueous media. The typical microgel has a spherical shape with a diameter ranging from 50 to 120 nm. It exhibits a zeta potential of −65 mV in a neutral aqueous medium; however, it may precipitate if the metastable colloidal dispersion state cannot be maintained. Its properties could be tailored through adjusting the internal chain conformation, highlighting its potential for diverse applications. Full article

When a horizontal electric field is applied, the sedimentation velocity of particles increases, a phenomenon known as Electrically Induced Rapid Separation (ERS). Hollow particles with a lower density than water exhibit an increased flotation velocity under an electric field. This study investigates the ERS effect in mixed suspensions containing particles denser than water and hollow particles with lower density. In the absence of an electric field, the denser particles settle while the hollow particles float, and their behavior is independent of the ratio of hollow particles to the total number of particles (α). However, when a DC electric field of 0.4 V/mm is applied, the behavior becomes dependent on α. For α < ~0.90, all particles sediment, whereas for α > ~0.93, all particles float. This suggests that the electric field induces a co-floc formation between the denser and hollow particles. Additionally, for the first time, a co-floc formation under an electric field was directly observed using a digital microscope. By adjusting α and applying an electric field, it is possible to control the sedimentation, flotation, or stabilization of the particle system. This study provides new insights into electric field-assisted particle separation and highlights its potential applications in colloidal science and materials science. Full article

When an electric field is applied to or removed from colloidal particle aqueous dispersions, a reversible increase in sedimentation velocity of the colloidal particles, referred to as the Electrically Induced Rapid Separation (ERS) effect, is observed. While electrophoresis and other interfacial electrokinetic phenomena under applied electric fields are well-studied, the phenomena of particle aggregation and re-dispersion caused by the application and removal of the field remain largely unexplored despite their significance. Experiments using mixed aqueous dispersions of poly (methyl methacrylate) (PMMA) particles of different sizes revealed that applying an electric field induced the formation of co-flocs involving both large and small particles, significantly enhancing the sedimentation velocity. It was also observed that slight vibrational deformation hindered the ERS effect. Under uniform electrolyte concentration conditions, the ERS effect was found to depend on pH, with a stronger effect observed when the absolute value of the zeta potential was larger. These findings indicate that the presence of the electric double layer plays a crucial role in the manifestation of the ERS effect. The results of this study provide critical insights for the further application of the ERS effect. Full article

A new nanodevice based on gold nanoparticles (AuNPs) capped with poly(diethylvinylphosphonate) (PDEVP) has been synthesized, showing interesting photophysical and thermoresponsive properties. The synthesis involves a properly designed Yttriocene catalyst coordinating the vinyl-lutidine (VL) initiator active in diethyl vinyl phosphonate polymerization. The unsaturated PDEVP chain ending was thioacetylated, deacetylated, and reacted with tetrachloroauric acid and sodium borohydride to form PDEVP-VL-capped AuNPs. The NMR, UV–Vis, and ESI-MS characterization of the metal nanoparticles confirmed the formation of the synthetic intermediates and the expected colloidal systems. AuNPs of subnanometric size were determined by WAXD and UV–Vis analysis. UV–Vis and fluorescence analysis confirmed the effective anchoring of the thiolated PDEVP to AuNPs. The formation of 50–200 nm globular structures was assessed by SEM and AFM microscopy in solid state and confirmed by DLS in aqueous dispersion. Hydrodynamic radius studies showed colloidal contraction with temperature, demonstrating thermoresponsive behavior. These properties suggest potential biomedical applications for the photoablation of malignant cells or controlled drug delivery induced by light or heat for the novel PDEVP-capped AuNP systems. Full article

The work is devoted to the study of the influence of nitrogenous bases on the composition of oil and the structure of asphaltenes on their colloidal stability in solution. Model petroleum systems with a basic nitrogen content of 1, 2, and 3% wt. were used as objects of study. Asphaltene-like nitrogenous bases were obtained by thermolysis of model petroleum systems with different nitrogen contents. The results were obtained using elemental analysis, non-aqueous potentiometric titration, spectrophotometry, ¹H NMR spectroscopy, and liquid adsorption chromatography. It was established that the content of N_bas in asphaltenes increases by 0.3–1.3% wt. with the increase in quinoline content in petroleum components. Quinoline is incorporated into the supramolecular structure of asphaltenes and increases their average molecular weight by 650 amu. and aromaticity by 2%. The aggregative stability of asphaltenes decreases by 1.5–6 times with an increase in their average molecular weight and an increase in N_bas in their composition as a component of a dispersion medium. The colloidal stability of synthetic asphaltene-like substances, on the contrary, is due to the appearance of their molecular sequence of fragments containing N_bas in aromatic rings. Full article

The green synthesis of silver nanoparticles (AgNPs) can be developed using safe and environmentally friendly routes, can replace potentially toxic chemical methods, and can increase the scale of production. This study aimed to synthesize AgNPs from aqueous extracts of guarana (Paullinia cupana) leaves and flowers, collected in different seasons of the year, as a source of active biomolecules capable of reducing silver ions (Ag⁺) and promoting the stabilization of colloidal silver (Ag⁰). The plant aqueous extracts were characterized regarding their metabolic composition by liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS/MS), phenolic compound content, and antioxidant potential against free radicals. The synthesized AgNPs were characterized by UV/Vis spectrophotometry, dynamic light scattering (DLS), nanoparticle tracking analysis (NTA), transmission electron microscopy (TEM), and scanning electron microscopy coupled to energy-dispersive X-ray spectrometry (EDX). The results demonstrated that the chemical characterization indicated the presence of secondary metabolites of many classes of compounds in the studied aqueous extracts studied, but alkaloids and flavonoids were predominant, which are widely recognized for their antioxidant capabilities. It was possible to notice subtle changes in the properties of the nanostructures depending on parameters such as seasonality and the part of the plant used, with the AgNPs showing surface plasmon resonance bands between 410 and 420 nm using the leaf extract and between 440 and 460 nm when prepared using the flower extract. Overall, the average hydrodynamic diameters of the AgNPs were similar among the samples (61.98 to 101.6 nm). Polydispersity index remained in the range of 0.2 to 0.4, indicating that colloidal stability did not change with storage time. Zeta potential was above −30 mV after one month of analysis, which is adequate for biological applications. TEM images showed AgNPs with diameters between 40.72 to 48.85 nm and particles of different morphologies. EDX indicated silver content by weight between 24.06 and 28.81%. The synthesized AgNPs exhibited antimicrobial efficacy against various pathogenic microorganisms of clinical and environmental interest, with MIC values between 2.12 and 21.25 µg/mL, which is close to those described for MBC values. Therefore, our results revealed the potential use of a native species of plant from Brazilian biodiversity combined with nanotechnology to produce antimicrobial agents. Full article

Conductive polymers, such as polyaniline (PANI), have interesting applications, ranging from flexible electronics, energy storage devices, sensors, antistatic or anticorrosion coatings, etc. However, the full exploitation of conductive polymers still poses a challenge due to their low processability. The use of compatible stabilizers to obtain dispersible and stable colloids is among the possible solutions to overcome such drawbacks. In this work, potato starch was used as a steric stabilizer for the preparation of colloidal polyaniline (emeraldine salt, ES)/starch composites by exploiting the oxidative polymerization of aniline in aqueous solutions with various starch-to-aniline ratios. The polyaniline/starch bio-composites were subjected to structural, spectroscopic, thermal, morphological, and electrochemical analyses. The samples were then tested for their dispersibility/solubility in a range of organic solvents. The results demonstrated the formation of PANI/starch biocomposites with a smaller average size than starch particles, showing improved aqueous dispersion and enhanced solubility in organic solvents. With respect to previously reported PANI-EB (emeraldine base)/starch composites, the novel colloids displayed a lower overall crystallinity, but the conductive nature of PANI-ES enhanced its electrochemical properties, resulting in richer redox chemistry, particularly evident in its oxidation behavior, as observed through cyclic voltammetry. Finally, as proof of the improved processability, the colloids were successfully integrated into a thin polyether sulfone (PES) membrane. Full article

Many physical and chemical properties of solids, such as strength, plasticity, dispersibility, solubility and dissolution are determined by defects in the crystal structure. The aim of this work is to study in situ dynamic, dispersion, chemical, biological and surface properties of lacosamide powder after a complete cycle of mechanical loading by laser scattering, electron microscopy, FR-IR and biopharmaceutical approaches. The SLS method demonstrated the spontaneous tendency toward surface-energy reduction due to aggregation during micronisation. DLS analysis showed conformational changes of colloidal particles as supramolecular complexes depending on the loading time on the solid. SEM analysis demonstrated the conglomeration of needle-like lacosamide particles after 60 min of milling time and the transition to a glassy state with isotropy of properties by the end of the tribochemistry cycle. The following dynamic properties of lacosamide were established: elastic and plastic deformation boundaries, region of inhomogeneous deformation and fracture point. The ratio of dissolution-rate constants in water of samples before and after a full cycle of loading was 2.4. The lacosamide sample, which underwent a full cycle of mechanical loading, showed improved kinetics of API release via analysis of dissolution profiles in 0.1 M HCl medium. The observed activation-energy values of the cell-death biosensor process in aqueous solutions of the lacosamide samples before and after the complete tribochemical cycle were 207 kJmol⁻¹ and 145 kJmol⁻¹, respectively. The equilibrium time of dissolution and activation of cell-biosensor death corresponding to 20 min of mechanical loading on a solid was determined. The current study may have important practical significance for the transformation and management of the properties of drug substances in solid form and in solutions and for increasing the strength of drug matrices by pre-strain hardening via structural rearrangements during mechanical loading. Full article

Nanocellulose, a nanoscale derivative from renewable biomass sources, possesses remarkable colloidal properties in water, mechanical strength, and biocompatibility. It emerges as a promising bio-based dispersing agent for various nanomaterials in water. This mini-review explores the interaction between cellulose nanomaterials (nanocrystals or nanofibers) and water, elucidating how this may enable their potential as an eco-friendly dispersing agent. We explore the potential of nanocellulose derived from top-down processes, nanocrystals, and nanofibers for dispersing carbon nanomaterials, semiconducting oxide nanoparticles, and other nanomaterials in water. We also highlight its advantages over traditional methods by not only effectively dispersing those nanomaterials but also potentially eliminating the need for further chemical treatments or supporting stabilizers. This not only preserves the exceptional properties of nanomaterials in aqueous dispersion, but may even lead to the emergence of novel hybrid functionalities. Overall, this mini-review underscores the remarkable versatility of nanocellulose as a green dispersing agent for a variety of nanomaterials, inspiring further research to expand its potential to other nanomaterials and applications. Full article