Search Results (290)

In this study, the rapidly setting and hardening high-belite sulfoaluminate cement (HBSAC) is used as the cementitious material, with natural river sand as the fine aggregate, and a high-performance repair mortar is prepared through the synergistic use of different polymers and admixtures. The influences of two polymers (VAE and HPMC) on the working performance, mechanical properties, and hydration characteristics of HBSAC mortars are systematically studied. The results showed that the two polymers had a significant improvement effect on the setting time, mortar flowability, and water retention rate of HBSAC mortar. Among them, VAE had a significant effect on the mortar flowability, and a 5% content could increase the flowability of HBSAC mortar by 29.8%. HPMC has a significant improvement effect on setting time and water retention rate; at 0.1% content, it can delay the initial setting time by 6.5 min and achieve a water retention rate of over 90%. As the polymer to binder ratio increases, both polymers, except for 2.5% VAE, which can slightly improve the flexural strength of mortar, will reduce the flexural and compressive strength of mortar, with VAE causing greater damage to strength. On the contrary, the polymer significantly enhanced the bond strength of the mortar. Compared with the cement control group, the 28 d bond strength of 5% VAE and 0.1% HPMC groups increased by 56.7% and 15.1%, respectively. Moreover, the addition of polymers delayed the occurrence of the exothermic peaks of HBSAC dissolution and ettringite formation, but the total amount of hydration heat released within 48 h was higher than that of pure cement. The diffraction peaks of AFt in the hydration products of VAE-HBSAC paste at 3d and 28d showed significant enhancement, and the peak intensity increased with higher doping levels, while the diffraction peak intensity of C₂S showed a certain decrease. The polymer significantly increased the weight loss peak intensity and mass loss after heating of AFt, AH₃, AFm, and C-S-H gel. The SEM images indicate that VAE can form a mesh on the surface of hydration products and refine the crystal size of AFt; HPMC wraps more flocculent substances around the hydration products, thereby improving the compactness of paste. This study can provide scientific reference for improving the performance and promoting the practical application of high-performance rapid repair mortar for concrete structure damage. Full article

Sodium caseinate (SC)-stabilized emulsions are highly susceptible to flocculation and phase separation near the protein isoelectric point (pI), limiting their application in acidified food systems. In this study, high acyl gellan gum (HA) was introduced to construct pH-responsive protein–polysaccharide complexes to modulate the interfacial assembly and stability of SC emulsions. Results demonstrated that HA interacts with SC primarily through electrostatic attraction and multi-site hydrogen bonding. This interaction induces protein conformational rearrangement and, as evidenced by combined structural and computational analyses, facilitates the assembly of a denser, interconnected composite network. The formation of HA–SC complexes significantly enhanced interfacial adsorption, reduced oil–water interfacial tension. Rheological and microrheological analyses revealed the composite system formed an elasticity-dominated weak gel network, restricting droplet mobility and suppressing aggregation. Consequently, HA–SC emulsions exhibited markedly improved pH tolerance and physical stability compared to SC-only emulsions, particularly near the pI, evidenced by reduced droplet size, lower Turbiscan stability indices, and more homogeneous microstructures. Crucially, utilizing a well-defined mechanistic model of fixed HA and SC concentrations, this study quantitatively links molecular interactions, interfacial network reconstruction, and macroscopic emulsion stability across a broad pH continuum. Rank-correlation analysis of pH-resolved descriptors shows the molecular charge state co-varies monotonically with the interfacial network and macroscopic stability, and is inversely coupled to droplet mobility. These findings provide new insights into protein–polysaccharide interfacial engineering, establishing the essential physical-stability foundation for the future rational design of acid-tolerant food emulsions and functional delivery systems. Full article

Microplastic contamination in soils is an emerging environmental challenge requiring effective and scalable remediation strategies. This review synthesizes advances in physical, chemical, biological, and hybrid approaches, focusing on mechanisms, performance, and practical applicability. Physical methods, particularly adsorption using biochar, achieve removal efficiencies exceeding 86% for 1 μm polystyrene microplastics and maintain > 85% efficiency after multiple reuse cycles, demonstrating strong durability. Filtration and aggregation systems, such as permeable reactive barriers, reach up to 81.55% removal but are less effective in co-contaminated conditions. Chemical strategies exhibit the highest efficiencies. Dielectric barrier discharge plasma achieves 96.5–98.7% degradation within 30–60 min, while electrochemical coagulation reaches ~98% removal via flocculation. Thermal treatments, including pyrolysis, enable near-complete microplastic removal (~100%) at ≥400 °C, although high energy demands limit in situ application. Chemical amendments also improve soil quality, increasing organic matter by ~7.35% and enhancing nutrient availability. Biological approaches offer sustainable but slower remediation. Microbial degradation achieves up to ~60% breakdown within 21 days, while enzyme–microbe systems reach ~21.4% over 60 days. Earthworm activity enhances fragmentation and nutrient cycling (up to 36.1%), whereas phytoremediation alone shows minimal direct degradation (<1% over 12 months). Hybrid strategies, particularly biochar-based systems, provide the most practical solutions by combining adsorption, microbial stimulation, and soil restoration, but their effectiveness in degrading microplastics needs further verification. These systems enhance microbial biomass (up to 57.67%), nutrient availability (up to 66.02%), and crop yield (up to 81.41%). Overall, physicochemical methods ensure rapid removal (>90%), biological approaches support long-term degradation, and hybrid systems offer scalable, sustainable remediation for field applications. Full article

Anaerobic digestion (AD) is an important method for sewage sludge (SS) stabilization and methane recovery. Fe compounds are widely present in SS because they are commonly used for phosphorus removal and organic matter (OM) capture in wastewater treatment plants. Endogenous Fe occurs in different forms, but the roles of these forms in SS AD remain unclear. This study systematically compared the effects of FeCl₃, Poly-FeCl₃, Fe₃O₄, FeOOH, and Fe₅HO₈·4H₂O on AD. The results showed that FeCl₃ and Poly-FeCl₃ decreased methane yield by 9.90% and 11.92%, respectively, whereas Fe₃O₄, FeOOH, and Fe₅HO₈·4H₂O increased it by 18.54%, 15.23%, and 15.09%. The analysis suggested that flocculating salts FeCl₃ and Poly-FeCl₃ groups increased sludge particle size, decreased SCOD concentrations by 10.21% and 12.41%, as well as F₄₂₀ by 16.88% and 28.63%, respectively, thereby inhibited the methanogenesis process. In contrast, Fe₃O₄, FeOOH, and Fe₅HO₈·4H₂O enhanced methane production by promoting OM hydrolysis, with SCOD concentrations increased by 12.71%, 8.99%, and 7.47%, respectively. XRD, CV, and EIS results showed that Fe₃O₄ likely promoted methanogenesis through a stable Fe(III)/Fe(II) cycle and electron transfer. Although FeOOH and Fe₅HO₈·4H₂O also underwent Fe(III)/Fe(II) conversion, their promoting effects were weaker than that of Fe₃O₄, possibly because the lack of a bulk mixed-valence structure reduced the efficiency of continuous electron transfer. This study highlights that the chemical form of Fe in SS fundamentally determines its effects on AD performance. Full article

In oil-rich countries, petroleum contamination of soils frequently occurs during refining, transportation, and exploitation. Such contamination significantly alters soil behavior and properties from a geotechnical perspective. Given that some fine-grained soils exhibit insufficient bearing capacity or excessive settlement, soil improvement is often necessary. The selective use of nanoparticles offers a promising novel approach in this regard. This study investigates the effects of diesel contamination and nanosilica modification on the physical and mechanical properties of clayey sand and aims to interpret the variations in the mechanical properties and the permeability of the treated soil based on microstructural observations. Diesel (0–10% in 2% increments) and nanosilica (0%, 1%, 2%) were added to the soil, preparing a total of 18 mixtures for testing. The microstructural changes directly alter the physical parameters such as specific gravity, optimum moisture content (OMC), and maximum dry unit weight, consequently affecting the permeability and the mechanical behavior. The microstructural analysis via scanning electron microscopy revealed diesel-induced clay flocculation and increasing macroporosity, while the nanosilica at 1% improved the soil fabric through pore filling and interparticle bonding, whereas 2% nanosilica led to partial dispersion and agglomeration. The findings demonstrate that soil behavior is controlled by the interplay between diesel (lubrication, pore blocking, hydrophobicity) and nanosilica (surface activation, micro-bonding, agglomeration). Increasing the diesel content consistently reduces the specific gravity across all the mixtures, due to the replacement of heavier mineral particles by lighter hydrocarbon, diesel adsorption onto the soil grains, the formation of low-density organic films, and increased micro-voids. Diesel addition reduces the OMC but increases the maximum dry unit weight due to its lubrication effect. Mechanically, the unconfined compressive strength (UCS) peaked at approximately 4% diesel contamination, with the addition of 1% nanosilica yielding the highest strength overall. Conversely, the California Bearing Ratio (CBR) increased continuously with diesel due to improved packing and frictional resistance and was further improved by nanosilica. The results show that permeability decreases with increasing diesel content due to hydrophobic diesel molecules coating soil particles, filling micro-voids, and blocking pore channels, while the consolidation parameters exhibit non-monotonic trends, peaking at moderate contamination levels. An optimal nanosilica content effectively mitigated some of the adverse effects of diesel and enhanced the mechanical performance, providing valuable insights for managing hydrocarbon-contaminated soils. Full article

Nitzschia sp., a diatom isolated from Paposo (Antofagasta, northern Chile), was evaluated as a biological solution for removing kaolinite-type clay minerals from recycled process water in large-scale copper mining. Optimization of culture conditions to maximize extracellular polymeric substance (EPS) production revealed that supplementing with 0.1 gL⁻¹ of glucose yielded the highest EPS levels on day 17, reaching 1285 ± 58.9 mgL⁻¹ (control equal to 237.8 ± 34 mgL⁻¹ on day 17). However, maximum dry weight biomass productivity was achieved in the presence of sodium carbonate at a concentration of 1 gL⁻¹ (319 ± 12.5 mgL⁻¹d⁻¹), significantly exceeding the productivity of the control group (242.7 ± 5.4 mgL⁻¹d⁻¹). Notably, low glucose supplementation enhanced EPS synthesis. Application of control-derived EPS of 1 gL⁻¹ rapidly decreased kaolinite initial turbidity from ~2024 FNU to ~354 ± 0.74 FNU within one minute. Even more glucose-derived EPS (1 gL⁻¹) further reduced turbidity to ~22.2 ± 0.1 FNU at 5 min, achieving a flocculation efficiency of ~98.9% after 15 min. Genomic analysis and KEGG annotation identified abundant genes for EPS and carbohydrate metabolism, including numerous glycosyltransferases, glycoside hydrolases, and multiple copies of UDP-glucose 4-epimerase, consistent with strong polysaccharide-biosynthesis capacity. Physicochemical characterization (particle sizing, HPLC, SEM, zeta-potential and FT-IR) showed EPS comprised mainly of rhamnose, fucose, arabinose, xylose and glucose, featuring functional groups (–OH, C=O/COO–, O-acetyl, uronic/guluronic signatures) that interact with kaolinite to promote aggregation. These findings demonstrate that Nitzschia-derived EPS, especially from glucose-supplemented cultures, represent promising sustainable bioflocculants for treating kaolinite-contaminated recycled water in mining operations. Full article

Soil hydrophysical properties play a key role in processes such as water movement through soil and also affect the amount of water available to plants, thus influencing the sustainability of water management in lowland agricultural landscapes. This study investigated whether the application of calcium sulfate dihydrate (gypsum, CaSO₄·2H₂O) can improve selected hydrophysical properties of a heavy clay agricultural soil from the Eastern Slovak Lowland (Slovakia). In a controlled laboratory experiment, topsoil samples (0–15 cm depth) were treated with four rates of gypsum application (0.5, 1, 2.5 and 10 g core⁻¹; ≈2–40 t ha⁻¹ equivalents) and then repacked in 100 cm³ cores. Gypsum caused a marked apparent shift from “clay” to “silt” in the particle-size analysis, consistent with flocculation and incomplete dispersion rather than a real textural change. Increasing the gypsum dose also led to a gradual increase in saturated hydraulic conductivity (from 0.68 ± 0.21 to 2.00 ± 0.66 cm d⁻¹). Water retention near saturation changed little, but water content at the wilting point decreased at higher doses, increasing plant-available water (maximum ~59% at 2.5 g core⁻¹). Under laboratory conditions, gypsum improved the hydraulic function of the soil, and, at selected doses, increased water availability related to drought, supporting its potential as a structural amendment for enhancing the sustainable management of heavy clay soils. Full article

This study reports the fabrication of Pickering emulsion gels stabilized by zein and curdlan (CU) and systematically elucidates the regulatory mechanisms of oil fraction and shearing parameters (temperature and duration) on their microstructure, mechanical properties, and stability. Results indicated that excessive oil content triggered pronounced flocculation and structural collapse, primarily attributed to insufficient interfacial coverage and compromised network continuity. An optimal dense network with superior cohesiveness was established at a shearing temperature of 60 °C, effectively entrapping oil droplets within the continuous phase. Furthermore, extending the shearing duration enhanced long-term stability by reducing droplet size, yielding a maximum oil binding capacity (OBC) of 78.9%. These emulsion gels exhibited remarkable stability against diverse environmental stressors, including thermal treatments, pH variations, and freeze-thaw cycles. This work expands the application of protein-polysaccharide complexes in food colloid science and provides a theoretical foundation for the development of novel low-fat food formulations based on emulsion gel systems. Full article

Water pollution due to insufficient wastewater treatment is a global concern. In this paper, coagulation and flocculation as a tertiary polishing unit process were investigated to find a solution for a non-compliant wastewater treatment facility. The Palapye Pond Enhanced Treatment and Operation (PETRO) system has not been compliant for a long time with effluent characterised by high turbidity, Biological Oxygen Demand/Chemical Oxygen Demand (BOD/COD), Total Suspended Solids (TSS), Nitrates (NO₃⁻), and Phosphates (PO₄³⁻) The effluent from the plant is released into the stream that drains into the nearby Lotsane dam, posing significant danger to the water quality of the dam. The main objective of the study was to investigate the effect of coagulation and flocculation processes at the tertiary stage of the wastewater treatment process. Response Surface Methodology (RSM), Central Composite Design (CCD) and Multi Response Surface (MRS) were used to optimise the coagulation process and generate regression models to predict the coagulation and flocculation. The performance was evaluated using turbidity, Colour, COD and TSS as response variables. Response surface analysis indicated that the experimental data could be adequately fitted to quadratic polynomial models. Under optimum conditions the removal efficiency for Al₂(SO₄)₃·18H₂O: 91.1% (turbidity), 88.2% (colour), 58.9% (COD), 83.0% (TSS); for FeCl₃·6H₂O: 93.2%, 88.7%, 63.8%, 91.3%; for Moringa: 91.8%, 85.4%, 56.6%, 83.7%. The optimal removals based on MRS for Al₂(SO₄)₃.18H₂O, FeCl₃.6H₂O and Moringa oleifera were 90.7%, 89.7%, 59.9% and 88.5%; 94.7%, 90.8%, 58.1% and 93.8%; 94.0%, 87.2%, 60.1% and 82.1% for turbidity, colour, COD and TSS respectively. This research has demonstrated that the coagulation/flocculation process, operating synergistically with pH-induced precipitation softening, can be incorporated as an enhancement to the secondary treatment stage of the wastewater treatment facility. At the optimal alkaline conditions (pH 12–12.6), the dominant mechanism is the precipitation of native hardness ions (Mg²⁺, Ca²⁺) as Mg(OH)₂ and CaCO₃, which enmesh colloidal particles, while the added coagulants play a refining role by enhancing floc structure and settling. The study introduces a comparative evaluation of three coagulants within a single RSM-CCD optimisation framework, employing desirability functions for multi-response optimisation. Full article

High-liquid-limit clay exhibits pronounced water sensitivity due to the strong electrostatic repulsion and weak interparticle bonding within its microstructure, which often limits its direct engineering uses and complicates the reuse of excavated clayey soils generated during the construction of transportation infrastructure. In this study, inorganic salts (KCl, CaCl₂ and FeCl₃) and carboxyl-containing polymers (PAAS, HPMA and CMC) were screened to construct organic–inorganic composite stabilization systems. Based on the screening results, an organic–inorganic composite system composed of CaCl₂ and sodium polyacrylate (PAAS) was developed to regulate interfacial interactions and induce microstructural reconstruction in clay. The synergistic mechanisms governing particle aggregation and dispersion were systematically investigated through Atterberg limit tests, zeta potential measurements, DLVO theoretical calculations, particle size analysis, scanning electron microscopy (SEM) and immersion disintegration experiments, combined with multivariate statistical modeling. Among the tested salt–polymer formulations, a composite system with 2% CaCl₂ and 0.1% PAAS showed the most favorable overall performance, achieving an optimal balance between electrostatic compression and steric stabilization, leading to enhanced structural integrity and delayed water-induced disintegration. Ca²⁺ ions compress the diffuse double layer and promote particle flocculation, whereas adsorbed PAAS chains introduce steric hindrance and interfacial modification. Their synergistic interaction reconstructs the pore–aggregate framework and regulates the interparticle potential energy landscape. DLVO analysis indicates that the optimized system attains a moderate critical interaction distance (h_c = 7.31 nm) and primary minimum depth (DPM = −2.72 × 10⁻¹⁶ J), reflecting a balanced interfacial bonding state. Multivariate statistical analyses further reveal a dual control pathway, in which consistency primarily governs disintegration duration, with additional contributions from surface electrochemical properties, while surface properties, soil structure and consistency collectively influence disintegration initiation. These findings elucidate the interfacial regulation and structural evolution mechanisms in organic–inorganic composite systems and provide insights into the design of composite modifiers for water-sensitive particulate materials, particularly for the resource reuse of high-liquid-limit clay excavated during the construction of transportation infrastructure and related geotechnical engineering applications. Full article

Micro- and nanoplastic pollution poses an emerging challenge for aquatic environments, driving the need for efficient and scalable removal strategies. Functional polymeric materials (FPMs) have emerged as a versatile platform to address this issue, owing to their tunable chemical composition, structural diversity, and ability to promote multiple removal mechanisms, including adsorption, filtration, and coagulation/flocculation. This review provides an overview of recent advances in polymer-based strategies for the removal of micro- and nanoplastics, with emphasis on material design, interaction mechanisms, and process performance. A broad range of materials, including natural hydrogels, polysaccharide aerogels, synthetic polymer composites, magnetic hybrids, and metal–organic frameworks (MOFs)–polymer systems, have demonstrated high removal efficiencies through electrostatic interactions, hydrogen bonding, hydrophobic effects, π–π stacking, and physical entrapment. Removal performance is strongly influenced by surface functionalization, porosity, surface area, and polymer network architecture, enabling targeted design for specific particle types and water matrices. Hybrid and multifunctional materials further enhance capacity and reusability, while natural polymers offer sustainable alternatives. Despite these advances, challenges remain in standardization, scalability, long-term stability, fouling resistance, and economic feasibility under realistic environmental conditions. Future research should focus on sustainable, multi-target, and scalable FPMs, integrating hybrid architectures, stimuli-responsive functionalities, and bioinspired design strategies. Particular attention should be given to mechanistic studies under environmentally relevant conditions and the establishment of structure–property design criteria to enable efficient removal of heterogeneous MPs/NPs mixtures. Overall, functional polymeric materials represent a flexible and high-performance platform for mitigating micro- and nanoplastic contamination, although their successful implementation will depend on bridging the gap between laboratory-scale performance and real-world water treatment applications. Full article

(1) Background: Flavored craft beer is favored for its diverse and distinctive aroma compounds; however, traditional fermentation processes are often plagued by poor yeast flocculation, which leads to substantial beer losses and compromised production efficiency. Yeast immobilization technology has emerged as a promising strategy to improve fermentation performance, shorten the primary fermentation period, and mitigate beer loss. (2) Methods: In this study, a natural material–based carrier was developed for the immobilization of yeast, and its application in mango craft beer fermentation was systematically investigated. The optimal fermentation conditions were screened, and the physicochemical properties, nutritional composition, and volatile flavor profiles of the resulting mango craft beer were comprehensively evaluated. (3) Results: The results showed that the maximum mass gain of yeast after immobilization on the natural carrier reached 13.3%. Compared with free yeast, the immobilized yeast exhibited a 1.58-fold higher average extract consumption rate and a 1.39-fold higher alcohol production rate based on the overall fermentation system, while the primary fermentation period was shortened by approximately 33%. Under the optimized fermentation conditions, the mango craft beer achieved a sensory score of 81 points, with a β-carotene retention rate of 91.25%. Furthermore, the mango craft beer exhibited a more diverse profile of volatile flavor compounds and enhanced nutritional composition compared with the control. (4) Conclusions: Overall, fermentation conditions were optimized using Response Surface Methodology (RSM) based on Box–Behnken Design (BBD). Natural immobilization carrier developed in this study effectively enhanced yeast fermentation efficiency and shortened the primary fermentation cycle, and these findings demonstrate its significant potential for cost reduction and efficiency enhancement in the production of flavored craft beer, providing a practical technical support for the industrial application of natural carrier-based yeast immobilization technology. Full article

This study provides novel insights into the gradual development of an algal-bacterial self-flocculent biomass in a 400 L pilot-scale raceway pond for wastewater treatment to enhance sustainability and minimize environmental footprint. The synergetic interaction of algal-bacteria consortia improves nutrient removal while enabling biomass concentration increase. Initially, the microalgae-bacteria biomass was gradually developed by increasing the operating volume from 60 to 400 L. After 80 days, the biomass reached a plateau at a concentration of about 4 g L⁻¹, and exhibited excellent settling characteristics. The initial settling velocity was 14.8 cm min⁻¹ and a settling time of 3 min was required to achieve efficient separation. The reactor achieved high treatment efficiency of about 95% for all nutrients (organic matter, nitrogen and phosphorous) after the 80th day. The kinetic analysis showed that nutrient removal followed first-order kinetics, with soluble chemical oxygen demand and ammonia removal reaching 0.017 and 0.020 h⁻¹, respectively. The results demonstrate high pollutant removal efficiencies and design guidelines for the use of increased concentrations of microalgae–bacteria consortia in urban wastewater treatment practice, an alternative green way for solving present-day wastewater treatment problems. Full article

Cadmium contamination of water resources represents a serious environmental and public health challenge, with conventional treatment methods often proving inadequate for industrial-level remediation. In this study, we present a novel, sustainable composite material, functionalized cellulose nanocrystal polyvinyl alcohol zinc oxide ferric chloride (CNC-PVA-ZnOFe) beads for the efficient removal of cadmium from contaminated water. The material integrates adsorption, coagulation, and flocculation mechanisms within a single hybrid platform, with coagulation–flocculation serving as the dominant mechanism given the material’s macroporous structure and limited surface area (1.2–3.3 m²/g). Functionalized cellulose nanocrystals provide supporting adsorptive sites for metal binding, while a PVA matrix incorporating ZnOFe improves structural integrity, mechanical stability, and coagulation performance. Characterization confirmed successful functionalization, enhanced thermal stability, and a macroporous structure (12–52 nm pores) conducive to floc entrapment, though with limited surface area (1.2–3.3 m²/g) for conventional adsorption. Under optimized conditions (pH 7–10, initial Cd²⁺ concentration of 100 mg/L, coagulant dose of 0.1 g, and sedimentation time of 60 min), the functionalized CNC-PVA-ZnOFe beads achieved a cadmium removal efficiency of 78%, achieving significantly higher cadmium removal efficiency than traditional coagulants, such as aluminum sulfate (69%). The beads also demonstrated good reusability, retaining 85% removal efficiency after five regeneration cycles. This work presents a scalable, eco-friendly material for cadmium removal under controlled laboratory conditions using synthetic solutions. However, further evaluation in real wastewater matrices containing competing ions and organic matter is necessary to establish practical applicability for water treatment applications. The study highlights the combined potential of multifunctional hybrid materials while acknowledging the need for validation under environmentally relevant conditions. While the results indicate successful integration of multiple removal mechanisms, direct validation of synergistic interactions through techniques such as zeta potential and XPS analysis remains an important direction for future research. Full article

This study explored the dual chemical modification of starch isolated from red lentils (Lens culinaris) to develop a biodegradable polymer with enhanced functionality for multifaceted applications. Native starch was isolated via combined salt–alkali treatment and sequentially modified through epichlorohydrin-mediated crosslinking, followed by cationization using glycidyl trimethylammonium chloride (GTAC). Utilizing a Quality by Design (QbD) strategy through Response Surface Methodology (RSM), the cationization endured fine-tuning to reach an optimal degree of substitution (DS = 0.572) under foremost conditions (GTAC: 2.1 mol, NaOH: 0.09 mol, reaction time: 18 h). Structural and functional characterization using FTIR, XRD, TGA, SEM, and zeta potential analysis confirmed the successful modification, indicating enhanced thermal stability, a transition to a more amorphous structure, and a moderately positive surface charge (+7.24 mV). The dual modified cationic lentil starch (CLS) demonstrated effective flocculation of kaolin suspensions, achieving a transmittance of up to 94%. Additionally, CLS showed significantly improved emulsion stability, maintaining over 70% stability after 24 h, compared to native starch, which dropped below 30%. These results emphasize the promising potential of CLS as an eco-friendly and high-performance alternative to synthetic polymers for water treatment and stabilization of emulsion-based formulations. Full article