Search Results (1,111)

Background: The addition of chlorhexidine in dental restorative materials is a promising strategy to reduce the recurrence of tooth decay lesions. However, the main challenge is to develop materials with antimicrobial activity in the long term. Objective: This study analyses the effect of filler type and concentration of resin composites supplemented with chlorhexidine loaded in carrier montmorillonite particles (MMT/CHX) regarding their chemical, physical, and short- and long-term antimicrobial proprieties. Materials: Experimental composites were synthesized with 0, 30, or 60% filler in two ratios, 70/30 and 80/20, of barium glass/colloidal silica, respectively, and 5 wt% MMT/CHX. Conversion was measured using near Fourier-transform infrared spectrometry. Sorption and solubility were determined by specimen weight before and after drying and immersing in water. Flexural strength (FS) and elastic modulus (E) were determined by three bending tests using a universal test machine. Chlorhexidine release was monitored for 50 days. Streptococcus mutans UA159 was used in all microbiological assays. Inhibition halo assay was performed for 12 months and, also, biofilm growth for the specimens and colony-forming unit (CFU). Remineralization assay was used on restored teeth using measurements of microhardness Knoop and CFUs. Results: Conversion, sorption, and solubility were not affected by filler type and concentration. FS and E increase with the filler concentration, independent from filler type. Chlorhexidine was significantly released for 15 days for all experimental materials, and the increase in filler concentration decreased its release. Halo inhibition was observed for a longer time (12 months) in materials with 60 wt% filler at 70/30 proportion. Also, 60 wt% filler materials, independent from the filler ratio, reduced the CFU in relation to the control group from 8 to 12 months. In the remineralization assay, besides the absence of differences in hardness among the groups, after biofilm growth, the CFU was also significantly lower in materials with 60 wt% filler. Conclusions: Materials with 60% filler, preferentially with 70% barium glass and 30% silica, and 5% MMT/CHX particles demonstrated long-term antimicrobial activity, reaching 12 months of effectiveness. Also, this formulation was associated with higher mechanical properties and similar conversion, sorption, and solubility compared to the other materials. Full article

Extensive studies have established that ultrasonic micro-jets and acoustic cavitation selectively intensify interfacial interactions at multiphase boundaries, thereby enhancing the flotation of soluble salt minerals and oxide ores. Although a growing body of evidence shows that pulp-borne nanoparticles (i.e., nanosolids, colloids, and nanoscale gas nuclei) mediate these effects, their role in the flotation of ultrafine smithsonite after collector addition has not yet been systematically examined. To fill this gap, we compared the flotation response of ultrafine smithsonite under conventional stirring (SC) and ultrasonic conditioning (UC), using sodium oleate (NaOL) as the collector, and dissected the governing mechanisms across three pillars, mineral–NaOL interaction, particle aggregation, and frothability, with particular attention paid to how nanoparticles modulate each dimension. The flotation results show that flotation performance under UC is dictated by NaOL concentration. At low NaOL levels (i.e., below 4 × 10⁻⁴ M), UC depresses both recovery and kinetics relative to SC, while at high NaOL levels, the trend reverses and UC outperforms SC. Mechanistic analysis reveals that sonication erodes mineral surfaces and generates cavitation, flooding the pulp with various nanoparticles. When NaOL is scarce, zinc-containing components and zinc-rich nanosolids sequester the collector through non-selective adsorption and precipitation, leaving smithsonite poorly hydrophobized. Consequently, particle aggregation and pulp frothability are markedly inferior to those in the SC system, so the flotation recovery and kinetics remain lower. As the NaOL concentration rises, smithsonite becomes adequately hydrophobized, and the pulp fills with hydrophobic zinc-rich nanosolids, along with cavitation-induced gas nuclei or tiny bubbles. These nanoparticles now act as bridges, accelerating the aggregation of ultrafine smithsonite once sonication stops and agitation begins, while simultaneously improving frothability. Although the strong dispersive action of ultrasound still suppresses initial flotation kinetics, cumulative recovery ultimately surpasses that of SC. The findings delineate a nanoparticle-regulated flotation paradigm and establish a critical NaOL concentration window for effective UC in ultrafine smithsonite flotation. This framework is readily transferable to the beneficiation of other ultrafine, soluble oxidized minerals (rhodochrosite, dolomite, etc.). Full article

In this study, the effects of biochar and compost on the amelioration of coastal saline soil were investigated through indoor leaching experiments and soil culture experiments. The results revealed that the multivoid structure of biochar and compost, when applied to soil, effectively improved soil hydraulic conductivity, promoted the leaching of salt ions, and reduced soil electrical conductivity. Owing to the high pH value of biochar and the lower pH value of compost, the combined application of the two has a complementary effect on improving the pH value of coastal saline soils. The calcium (Ca²⁺) and magnesium (Mg²⁺) contained in biochar and compost are exchanged with Na⁺ adsorbed by soil colloids, which reduces the sodium (Na⁺) adsorption ratio (SAR) value of the soil. Biochar and compost improve the physical properties of the soil, and the organic matter they contain helps soil particles aggregate with each other and form stable clusters, thus promoting the formation of soil agglomerates, which are conducive to the formation of clusters with a diameter of ≤0.25 mm. Biochar and compost are rich in nutrients, and their application significantly increased the contents of available nutrients and organic matter as well as the activities of urease, phosphatase, and dehydrogenase in saline soils. However, too high of an application rate of biochar increases the soil pH value, and excessive application of compost can lead to greater soil conductivity, which inhibits the activities of soil urease, phosphatase and dehydrogenase. Therefore, rational control of application rates is essential for improving coastal saline soils. Future research should further explore the synergistic effects of biochar and compost in improving soil structure, nutrient effectiveness, and microbial activity to promote their effective application in coastal saline–alkaline soil improvement. Full article

Fracture-induced loss poses severe challenges to drilling operations, particularly under high-temperature and high-salinity conditions encountered in deep wells. Conventional plugging materials, characterized by relatively large particle sizes and poor structural integrity, often exhibit insufficient thermal stability and salt tolerance under extreme drilling conditions, making them prone to structural degradation and loss of adhesion, which ultimately leads to drilling fluid deterioration and downhole complications. To address this issue, a core–shell-structured microgel, ANDT-70 (named after the acronyms of 2-acrylamido-2-methylpropane sulfonic acid, N-vinyl-2-pyrrolidinone, N, N-dimethylacrylamide, dimethyl diallyl ammonium chloride, and titanium dioxide nanoparticles), was synthesized and systematically evaluated for its thermal stability, salt resistance, and interfacial adhesion capabilities. The structural evolution, dispersion behavior, and colloidal stability of the microgel were thoroughly characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), Raman spectroscopy, and Zeta potential analysis. Experimental results indicate that ANDT-70 exhibits excellent thermal stability and resistance to salt-induced degradation at 260 °C, maintaining its fundamental structure and performance under harsh high-temperature and high-salinity conditions, with a viscosity retention of 81.10% compared with ambient conditions. Compared to representative materials reported in the literature, ANDT-70 exhibited superior tolerance to ionic erosion in saline conditions. AFM analysis confirmed that ANDT-70 significantly improves bentonite slurry dispersion and reduces salt sensitivity risks. ANDT-70 stably adsorbs onto bentonite lamellae via the synergistic action of electrostatic interactions and hydrogen bonding, thereby forming a dense cementation network that markedly enhances the structural stability and adhesion of the system. This network significantly enhances the cohesion and structural integrity of drilling fluid systems under extreme conditions. In conclusion, ANDT-70 demonstrates strong potential as a high-performance functional microgel for enhancing the stability and effectiveness of advanced drilling fluids under complex geological environments. Full article

Cutin is a natural plant polyester, a constituent of the cuticle that covers aerial plant surfaces. Following the trends of agricultural and food waste reduction and the growing demand for plant-derived nanomaterials, cutin was extracted from tomato peels, a by-product of tomato processing. Subsequently, dispersions of cutin particles in the nano- and colloidal size range were prepared by pH-dependent precipitation. Four types of the dispersions were obtained, i.e., dispersion from cutin extract—NP E dispersion, dispersions from a solution of different cutin isolates, dialyzed cutin isolate–NP D dispersion, washed cutin isolate–NP W dispersion, and standard cutin isolate–NP S dispersion. Cutin precipitation occurred at pH lower than 7 and cutin dispersions with final pH 3–7 were formed. Zeta potential, particle size, and recovery of four cutin dispersions were investigated. All types of cutin particles bear a negative charge which increases on pH increase from 3 to 7, resulting in decrease in cutin nanoparticle size upon pH increase. In addition to that, the influence of cutin solution concentration and storage time on cutin dispersion particle size was found to be mitigated at pH ≥ 6. Among four dispersions, NP S had the highest cutin nanoparticle recovery at all pHs investigated. Full article

The ice sheet and subglacial geological environment in Antarctica have become the focus of scientific exploration. The development of Antarctic drilling technology will serve as a crucial safeguard for scientific exploration. However, the extremely ultra-low temperatures and intricate geological conditions present substantial obstacles for drilling operations in Antarctica, and the existing drilling fluid technology cannot satisfy the requirements of efficient and safe drilling. To ameliorate the wettability and rheology of ultra-low-temperature drilling fluids, a new amide material (HAS) was prepared using dodecylamine polyoxyethylene ether, azelaic acid, and N-ethylethylenediamine as raw materials. Experiments using infrared spectroscopy, nuclear magnetic hydrogen spectroscopy, and contact angle indicated that the target product was successfully synthesized. Performance evaluation showed that 2% HAS could achieve a yield point of 2.5 Pa for drilling fluid at −55 °C, and it also gave the fluid superior shear-thinning characteristics and a large thixotropic loop area. This indicated that HAS significantly enhanced the rheological properties of the drilling fluid, ensuring that it can carry cuttings and ice debris. In addition, 2% HAS could also increase the colloidal rate from 8% to more than 76% at −55 °C in different base oils. Meanwhile, the colloid rate was maintained above 92.4% when the density was 0.92~0.95 g/cm³. Mechanism studies showed that HAS increased the zeta potential and decreased the particle size of organoclay. At the same time, it changed the organoclay state from a clustered state to a uniformly dispersed state, and the particle size decreased. It was found that HAS formed a weak gel grid structure through interactions between polar groups, such as amide and imino groups with organoclays particles, thus improving the rheology and wettability of drilling fluid. In addition, HAS is an environmentally friendly high-performance material. Full article

This study involved developing a Pickering emulsion system based on a composite material comprising zein colloidal particles (ZCPs) and cellulose nanocrystals (CNCs) with the aim of exploring its potential application in fruit preservation by loading carvacrol (CAR). The system (CAR@ZCPE) consists of ZCP particles with an average size of approximately 317 nm in a composite with CNC particles of approximately 85 nm at an optimal mass ratio (ZCP/CNC = 1:3) to form stable particles encapsulating CAR. The results indicate that CAR@ZCPE is an O/W Pickering emulsion that can be diluted indefinitely in water and exhibits excellent environmental stability. Rheological analysis revealed that it exhibits shear-thinning properties and a gel-like network structure, which explains its good stability. Bioactivity evaluation revealed that CAR@ZCPE exhibited inhibitory activity against Botryosphaeria dothidea, with an inhibition rate of 63.60% at a concentration of 50 mg/L. Kiwifruit preservation experiments confirmed that CAR@ZCPE significantly reduced the degree of kiwifruit decay, and cell activity evaluations confirmed its biosafety. The total apoptotic rate of LO2 cells was 2.10%, indicating that the emulsion did not affect the cell growth cycle. This study successfully developed a CAR Pickering emulsion stabilized by ZCP-CNC composite particles. This emulsion system combines high stability, excellent antibacterial activity, and excellent biocompatibility. Kiwifruit preservation experiments validated its potential as a safe and efficient new preservative, providing an innovative method for preserving fruits using ZCP-CNC-composite-stabilized Pickering emulsions. Full article

This study examined a novel ethoxy-segment-regulated hydrophobic associative amphiphilic copolymer, P(AA-AAEO_n), and systematically evaluated its solution self-assembly behavior and enhanced oil recovery (EOR) performance. The influence of ethylene oxide (EO) chain length and polymer concentration on particle size distribution and aggregation morphology was analyzed using dynamic light scattering (DLS). The results revealed a concentration-dependent transition from intramolecular to intermolecular association, accompanied by a characteristic decrease followed by an increase in hydrodynamic diameter. At a fixed AA:AAEO_n molar ratio (400:1), increasing EO segment length increased aggregate size and improved colloidal stability. Viscometric analysis showed that longer EO chains markedly increased molecular chain flexibility and solution viscosity. Interfacial tension measurements demonstrated superior interfacial activity of P(AA-AAEO_n) compared to polyacrylic acid (PAA), and longer EO chains further reduced oil–water interfacial tension. Emulsification tests verified its strong ability to emulsify crude oil. Sandpack flooding experiments and micromodel studies demonstrated effective conformance control and high displacement efficiency, achieving up to 30.65% incremental oil recovery. These findings offered essential insights for designing hydrophobic associative polymers with tunable interfacial properties for EOR applications. Full article

The self-consistent field Poisson–Boltzmann framework is applied for analysis of equilibrium partitioning of ampholytic protein-like nanocolloids between buffer solution and weak (pH-sensitive) versus strong polyelectrolyte (polyanionic) brushes with the same net charge per unit area. The position-dependent nanocolloid net charge and the insertion freeenergy profiles are derived as a function of pH and ionic strength in the solution. It is demonstrated that, similar to strong polyelectrolyte brushes, pH-sensitive brushes are capable of the uptake of nanocolloids in the vicinity of the isoelectric point, that is, when the net charge of the colloid in the buffer has either the opposite or the same sign as the ionized monomer units of the brush. At $pI\ge p{K}_{brush}$ and $pH\ge pI$, the particle absorption patterns by similarly (negatively) charged brushes are qualitatively similar in the cases of strong and weak polyelectrolyte brushes, but the freeenergy barrier at the brush periphery is wider for weak than for strong polyelectrolyte brushes, which may cause stronger kinetic hindrance for the nanocolloid uptake by the brush. A decrease in $pH$ below the IEP leads to a monotonic increase in the depth of the insertion freeenergy minimum inside a strong polyelectrolyte brush, whereas for weak polyelectrolyte brushes, a more peculiar trend is predicted: due to competition between the increasing positive charge of the nanocolloid and the decreasing magnitude of the negative charge of the brush, the absorption is weakened at low $pH$. Full article

Diffusiophoresis of a liquid metal droplet (LMD) in a cylindrical pore is investigated theoretically in this study. A patched pseudo-spectral method based on Chebyshev polynomials combined with a geometric mapping technique is adopted to solve the resulting governing electrokinetic equations in irregular geometries. Several interesting phenomena are found which provide useful guidelines in practical applications involving liquid metal droplets (LMDs) such as drug delivery. In particular, the severe boundary confinement effect brings about unique features of droplet motion, leading to mobility reversal and a “stagnation phenomenon” where droplets cease to move regardless of their surface charge densities in a narrow cylindrical pore. An overwhelming exterior vortex flow nearly enclosing the entire droplet is found to be responsible for this. This finds various practical applications in droplet microfluidics and drug delivery. For instance, a cylindrical pore or blood vessel may be clogged by a droplet much smaller than its radius. In addition, the “solidification phenomenon”, where all droplets move with identical speed regardless of their viscosities like rigid particles with no interior recirculating vortex flows, is also discovered. The electrokinetic mechanism behind it and its potential applications are discussed. Overall, the geometric configuration considered here is a classic one, with many other possible applications yet to be found by experimental researchers and engineers in the field of colloid industry and operations. Full article

Colloidal quantum dots (QDs) are semiconductor crystals a few nanometers in size. Due to their vibrant colors and unique photoluminescence (PL), QDs are widely utilized in displays, where barrier films provide essential shielding. However, one of the primary challenges of QD applications remains achieving sufficient robustness while keeping costs low. Over the past two decades, significant progress has been made in the encapsulation of QDs within silica matrices, aiming to preserve their original PL properties. Research efforts have evolved from bulk forms to thin films. Silica nanoparticles containing multiple embedded QDs have emerged as particularly promising candidates for practical applications. This review highlights recent advancements in silica-based QD encapsulation, incorporating findings from both the authors’ investigations and those of other research groups within the field. Silica glass possesses inherent shielding capabilities, but silane coupling agents such as (3-aminopropyl)trimethoxysilane and (3-mercaptopropyl)trimethoxysilane tend to negatively impact this functionality when they are used alone, partly because of the limited formation of a well-developed glass network structure. However, when judiciously controlled, they can serve as mediators between the QD surface and the surrounding pure silica glass matrix, helping to preserve PL properties and control the morphology of silica particles. This review discusses the potential for achieving exceptional shielding properties through sol–gel glass fabrication at low temperatures, utilizing both tetraethoxysilane and other silane coupling agents. Full article

In this paper, a silver thin film coating on a monolayer polystyrene colloidal crystal (MPCC) hybrid structure was fabricated, and a photonic–surface plasmon coupling mode was established and experimentally researched. The silver thin film was sputtered onto the MPCC to form Ag-MPCC. The silver film effectively excites surface plasmon polariton (SPP) modes upon the incidence of light, and the MPCC has an intrinsic mode. These two modes couple and result in the extraordinary optical transmission (EOT) phenomenon in the transmission spectrum. Reflection suppression arising from this photon coupling effect was discovered in the reflection spectrum. We etched the single-layer colloidal particles to change the period of the colloidal crystal, thereby forming the MPCC metal hybrid structure with different lattices. We discussed and analyzed the results through experiments. The EOT can be controlled by the incident angle, lattice periodicity, and refractive index distribution of the Ag-MPCC, and the diffraction behavior is determined using the lattice structure and refractive index of the MPCC. The coupling effect of the two models leads to wavelength shifts and intensity variations in the spectral eigenvalues. Reflection suppression is achieved when the reflectivity at a specific wavelength is close to 0.1. Full article

Inland aquatic ecosystems, encompassing lakes, reservoirs, and ponds, serve as vital repositories of water resources and provide essential ecological, social, and cultural services. Water color, a key indicator of water quality, reflects the complex interactions among physicochemical, biological, and environmental drivers. Heilong Pool (HP) in Southwest China, which consists of a Clear Pool (CP) and a Turbid Pool (TP), has recently exhibited an anomalous reddish-brown “pumpkin soup” phenomenon in the CP, while the TP remains unchanged. This unusual phenomenon has raised widespread public concern regarding water resource security and its potential association with geological disasters. To elucidate the ecological and geochemical mechanisms of this phenomenon, we employed a multifaceted analytical approach that included assessing nutrient elements, quantifying heavy metal concentrations, analyzing dissolved substances, characterizing algal community composition, and applying δD-δ¹⁸O isotope analytical models. Our findings illustrated that while Bacillariophyta predominate (>79.3% relative abundance) in the algal community of HP, they were not the primary determinant of water color changes. Instead, Fe(OH)₃ colloidal particles, originating from groundwater–surface water interactions and controlled by redox environment dynamics periodically, emerged as the principal factors of the reddish-brown discoloration. The genesis of the “pumpkin soup” water coloration was attributed to the precipitation-induced displacement of anoxic groundwater from confined karst conduits. Subsequent exfiltration and atmospheric exposure facilitate oxidative precipitation, forming authigenic rust-hued Fe(OH)₃ colloidal complexes. This study provides new insights into the geochemical and hydrological mechanisms underlying water color anomalies in karst-dominated catchments. Full article

Highly alkaline and highly toxic red mud and other bulk industrial solid wastes become severely accumulated, posing huge risks such as soil degradation and environmental pollution. It is urgent to develop a long-term and stable resource disposal method. In the present research, artificial lightweight aggregates were fabricated utilizing industrial solid residues including red mud, phosphate tailing powder, and fly ash as raw materials. The physical characteristics, microstructure, heavy metal leaching attributes, and freeze–thaw resistance under different mixed water and curing conditions were studied. The results showed that, under the optimal curing condition (steam curing temperature of 80 °C and curing time of 10 h), lightweight aggregates exhibited the best comprehensive performance, with favorable trends in bulk density, apparent density, softening coefficient, and 1 h water absorption. In addition, the impact of extending the curing time on the further enhancement of the cylinder crush strength is limited. The microscopic morphology study showed that the hydration products in lightweight aggregates are primarily N-A-S-H and C-(A)-S-H, forming a strong colloidal structure and evenly dispersed on the particle surface, thereby improving its strength. Moreover, the heavy metal leachates (Cr, Pb, As, Cu, and Ni) from the lightweight aggregates met the environmental discharge criteria for non-hazardous substances. Full article

Dye residues from the textile industry constitute a critical wastewater problem. This study aimed to evaluate the removal capacity of methylene blue (MB) in aqueous media, using an adsorbent formulated from activated and sonicated nanoclay (NC) and microatomized Nostoc sphaericum (ANS). NC was obtained by acid treatment, followed by activation with 1 M NaCl and sonication, while ANS was obtained by microatomization in an aqueous medium. NC/ANS was mixed in a 4:1 weight ratio. The NC/ANS synergistic adsorbent was characterized by the point of zero charge (PZC), zeta potential (ζ), particle size, FTIR spectroscopy, and scanning electron microscopy (SEM). NC/ANS exhibited good colloidal stability, as determined by pH_PZC, particle size in the nanometer range, and heterogeneous morphology with functional groups (hydroxyl, carboxyl, and amide), removing between 72.59 and 97.98% from an initial concentration of 10 ppm of MB, for doses of 20 to 30 mg/L of NC/ANS and pH of 5 to 8. Optimal adsorption conditions are achieved at pH 6.8 and 32.9 mg/L of adsorbent NC/ANS. It was observed that the pseudo-first-order (PFO) and pseudo-second-order (PSO) kinetic models best described the adsorption kinetics, indicating a predominance of the physisorption process, with adsorption capacity around 20 mg/g. Isotherm models and thermodynamic parameters of adsorption, ΔS, ΔH, and ΔG, revealed that the adsorption process is spontaneous, favorable, thermodynamically stable, and occurs at the monolayer level, with a regeneration capacity of 90.35 to 37.54% at the fifth cycle. The application of physical activation methods, such as sonication of the clay and microatomization of the algae, allows proposing a novel and alternative synergistic material from organic and inorganic sources that is environmentally friendly and promotes sustainability, with a high capacity to remove cationic dyes in wastewater. Full article