Search Results (453)

The textile industry’s reliance on synthetic dyes contributes significantly to pollution, highlighting the need for sustainable alternatives like biopigments. This study investigates the production and application of the biopigment prodigiosin, which was produced by Pseudomonas putida with a yield of 1.85 g/L. Prodigiosin was prepared under acidic, neutral, and alkaline conditions, resulting in varying protonation states that influenced its affinity for cotton and polyester fibers. Three surfactants (anionic, cationic, non-ionic) were tested, with non-ionic Tween 80 yielding a promising color strength (above 4) and fastness results with neutral prodigiosin at 1.3 g/L. Cotton and polyester demonstrated good washing (color difference up to 14 for cotton, 5 for polyester) and light fastness (up to 15 for cotton, 16 for polyester). Cellulose acetate, used in the conventional printing process as a thickener, produced superior color properties compared to commercial thickeners. Neutral prodigiosin achieved higher color strength, and cotton fabrics displayed halochromic properties, distinguishing them from polyester, which showed excellent fastness. Prodigiosin-printed samples also exhibited strong antimicrobial activity against Pseudomonas aeruginosa and retained halochromic properties over 10 pH cycles. These findings suggest prodigiosin as a sustainable dye alternative and pH sensor, with potential applications in biomedical materials, such as antimicrobial and pH-responsive wound dressings. Full article

Relaxation behavior of water confined in reverse micelles under temperature-induced micelle clustering is undertaken using broadband dielectric spectroscopy in frequency range 1 Hz–20 GHz. All microemulsion systems with sufficiently noticeable micelle water pool (water/surfactant molar ratio W > 10) depict three relaxation processes, in low, high and microwave frequencies, anchoring with relaxation of shell (bound) water, orientation of surfactant anions at water-surfactant interface and relaxation of bulk water confined in reverse micelles. The analysis of dielectric relaxation processes in AOT-based w/o microemulsions under temperature induced clustering of reverse micelles were made according to structural information obtained in NMR and conductometry experiments. The “wait and switch” relaxation mechanism was applied for the explanation of results for water in the bound and bulk states under spatial limitation in reverse micelles. It was shown that surfactant layer predominantly influences the bound water. The properties of water close to AOT interface are determined by strong interactions between water and ionic AOT molecules, which perturb water H-bonding network. The decrease in micelle size causes a weakening of hydrogen bonds, deformation of its steric network and reduction in co-operative relaxation effects. Full article

This study presents the first quantitative comparison of catastrophic phase inversion behavior of water-in-oil emulsions stabilized by nanocrystalline cellulose (NCC) and molecular surfactants with different headgroup charge types: anionic (sodium dodecyl sulfate referred to as SDS), cationic (octadecyltrimethylammonium chloride referred to as OTAC), nonionic (C12–14 alcohol ethoxylate referred to as Alfonic), and zwitterionic (cetyl betaine referred to as Amphosol). By using conductivity measurements under controlled mixing and pendant drop tensiometry, this study shows that NCC markedly delays catastrophic phase inversion through interfacial jamming, whereas surfactant-stabilized systems exhibit concentration-dependent inversion driven by interfacial saturation. Specifically, NCC-stabilized emulsions exhibited a nonlinear increase in the critical aqueous phase volume fraction required for inversion, ranging from 0.253 (0 wt% NCC) to 0.545 (1.5 wt% NCC), consistent with enhanced resistance to inversion typically associated with the formation of rigid interfacial layers in Pickering emulsions. In contrast, surfactant-stabilized systems exhibited a concentration-dependent inversion trend with opposing effects. At low concentrations, limited interfacial coverage delayed inversion, while at higher concentrations, increased surfactant availability and interfacial saturation promoted earlier inversion and favored the formation of oil-in-water structures. Pendant drop tensiometry confirmed negligible surface activity for NCC, while all surfactants significantly lowered interfacial tension. Despite its weak surface activity, NCC imparted strong coalescence resistance above 0.2 wt%, attributed to steric stabilization. These findings establish distinct mechanisms for governing phase inversion in particle- versus surfactant-stabilized systems. To our knowledge, this is the first study to quantitively characterize the catastrophic phase inversion behavior of water-in-oil emulsions using NCC. This work supports the use of NCC as an effective stabilizer for emulsions with high internal phase volume. Full article

This study focuses on the design and optimization of a monopolar electrode configuration for the hybrid electrochemical treatment of real washing machine wastewater. A combined electrocoagulation (EC) and electro-oxidation (EO) system was optimized to maximize pollutant removal efficiency while minimizing energy consumption. The monopolar setup employed mixed metal oxide (MMO) and aluminum anodes, along with a stainless steel cathode, operating under controlled conditions with sodium chloride as the supporting electrolyte. An applied current density of 15 mA cm⁻² achieved 90% chemical oxygen demand (COD) removal, 98% surfactant degradation, complete turbidity reduction within 120 min, and pH stabilization near 8. Additionally, electrochemical disinfection achieved <2 MPN/100 mL, with no detectable phenols and the presence of organic anions such as oxalate and acetate. These results demonstrate the effectiveness of an optimized monopolar EC–EO system as a cost-efficient and sustainable strategy for wastewater treatment and potential water reuse. Further studies should focus on refining energy consumption and monitoring reaction by-products to enhance large-scale applicability. Full article

In this paper, the basic concept of surfactants as chemical additives and their diversified classification system are first expounded, laying a theoretical foundation for the subsequent study of their application in demulsification technology. Then, the specific application cases of various types of surfactants in the field of demulsification are deeply analyzed, and ways in which they achieve effective separation of emulsions through their unique physical and chemical properties are revealed. Further, the internal action mechanism of surfactant demulsifier, including how to destroy the stability of emulsion and promote the separation of oil and water phase, is systematically described. On this basis, the significant advantages of surfactant demulsifier compared with traditional methods are summarized, including high cost-effectiveness, high demulsifier efficiency, strong stability, wide adaptability, and easy operation. Finally, the development direction and challenges of surfactant demulsifier in the future are prospected. Full article

This study proposes a method for separating asphalt and aggregates in recycled asphalt pavement (RAP) materials using surfactants as solvents. This method utilizes surfactants to soften the asphalt by reducing its surface tension, separating the RAP clusters, and washing away the asphalt from the RAP. The wastewater is recycled during the emulsification–separation process without discharge. Factors affecting the separation effect of RAP, including the type of anionic surfactants, the surfactant concentration, the emulsion-to-RAP ratio, temperature, the rotation rate and time, and the RAP’s particle size, were investigated in depth, and the separation effect and its influence on the aggregate properties were evaluated. The experimental results indicate that when using the optimal process to mix and treat 13.2 mm and 9.5 mm RAP clusters, it is possible to achieve 100% separation of the coarse RAP above 4.75 mm, with a 64.58% reduction in the asphalt content. The angularity of the aggregate remained unchanged after separation. It was observed from scanning electron microscopy (SEM) images that the asphalt on the surface of the coarse aggregate had been eluted, and the morphology of the aggregate surface was completely exposed. This environmentally friendly separation method provides new possibilities for high-content RAP recycling in pavement engineering. Full article

The paper is devoted to the plasticization mechanisms of alkali-activated cement system Na₂O-CaO-Al₂O₃-SiO₂-H₂O. The fundamentals and basic factors determining the effectiveness of plasticizing surfactants for alkali-activated cement materials are discussed. The factors under consideration in the study were alkali-activated cement basicity (the content of granulated blast furnace slag), the anion of the alkaline component or activator, and the degree of dispersing of the cement particles in the system. The action effect of plasticizers was determined by finding the interrelation between the stability of its molecular structure, degree of adsorption, and molecular weight depending on mentioned basic factors. A systematic approach to the systematization of surfactants and their choice to be taken into consideration to control technology-related and physico-mechanical properties of alkali-activated cement-based heavyweight concretes, building mortars, and lightened grouts has been proposed. Full article

Piping is a severe threat to dikes, which can lead to dike failure, and cause significant economic and human casualties. However, conventional measures necessitate substantial labor and material resources. A novel foam-based method for the rapid mitigation of piping was proposed to enhance piping emergency control efficiency, which demonstrates significant application potential. This study aims to develop a novel foam formulation and evaluate its performance in controlling piping in dikes. Through a combination of foam static-property characterization experiment and foam plugging capacity assessment experiment, a compounded anionic–cationic surfactant composed of sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) is optimized. The formulation, at a 9:1 mass ratio and 1.5% total concentration, exhibits superior foam stability and plugging performance. An experiment on the ability of the foam to restrain piping demonstrated that, compared to single-component SDS foam, the compounded SDS-CTAB foam increased the critical hydraulic gradient for piping from 2.35 to 2.70, a 15% improvement. It also reduces the extent of piping channel development under equivalent hydraulic conditions. The foam storage area exhibits enhanced scour resistance and better preservation under prolonged water flow. Mechanistically, the SDS-CTAB foam benefits from synergistic hydrophobic interactions, electrostatic attraction, and hydrogen bonding between surfactant molecules, which enhance foam stability. Full article

Clogging in earth pressure balance (EPB) shield tunnelling through highly cohesive strata critically undermines construction efficiency. Conventional foam agents exhibit limited conditioning effectiveness, even with increased dosage. This study developed a dispersed foam agent by combining anionic surfactant (AES) with nonionic dispersant (HDT). The effects of air pressure (0–2 bar) and HDT content (0–10%) on macro-meso characteristics of foam and adhesion characteristics of conditioned soil were quantified through an evolutionary mechanism investigation of the bubble size distribution of foam, half-life measurements, and mechanical tests on conditioned soils. Results demonstrated that the influence of HDT content on foam exhibited pressure-dependent behavior. Under 0 bar within 0–10 min, HDT increased the proportion of small bubbles while marginally reducing the mean radii. Although HDT accelerated the degradation of small bubbles, it extended the foam half-life. Conversely, under 1 or 2 bar, HDT demonstrated opposite effects on these parameters. The cohesion of conditioned clays was reduced to 1.8–4.3 kPa, and adhesion amounts decreased to 10–15 g, significantly mitigating clogging risks. The optimal injection ratio of dispersed foam was determined for different pressures and clays. Engineering application in an EPB shield tunnelling section of Jinan Metro successfully resolved clogging issues, demonstrating the effectiveness of dispersed foam agent. Full article

Soil washing is an efficient method to remove polybrominated diphenyl ethers (PBDEs) from contaminated soils. The obtained solutions from soil-washing still contain PBDEs, requiring further treatment before disposal or reuse. Although photolysis is effective for PBDE degradation in solutions, the concurrent formation of toxic polybrominated dibenzofurans (PBDFs) may limit its practical application. In this study, 2,8-dibromodibenzofurans (2,8-BDF) formation rate and mechanisms during 2,4,4′-tribromodiphenyl ether (BDE-28) photolysis in various simulated soil-washing solutions was investigated. Results revealed significant effects of solubilizers on 2,8-BDF formation. The nonionic surfactants polysorbate (TW80), polyoxyethylene octylphenyl ether (TX series), and the cationic surfactant cetyltrimethylammonium bromide (CTAB) resulted in low 2,8-BDF formation rate (1–5%), while the β-cyclodextrin led to the highest 2,8-BDF formation rate (about 28%). The nonionic surfactants polyoxyethylene dodecyl ethers (Brij series), and the anionic surfactants sodium dodecylbenzene sulfonate (SDBS) and sodium dodecyl sulfate (SDS), also showed a high level of 2,8-BDF formation rate (7–17%). Solubilizer structure and its interaction with BDE-28 determined the 2,8-BDF formation. The role of the micelle microenvironment on 2,8-BDF formation was verified via an experiment and molecular dynamics simulation. The organic region of micelle exhibited high hydrogen donation ability, which inhibited 2,8-BDF formation. The results indicated distinct risks of PBDE photolysis in various soil-washing solutions, providing an important reference for solubilizer selection and the application of photolysis on the treatment of soil-washing solutions containing PBDEs. Full article

Although the intercalation of sericite with cationic surfactants has been extensively studied, successful intercalation using anionic surfactants has yet to be achieved. This article aims to partially or fully intercalate sericite with an anionic surfactant, and to develop the corresponding sericite/polymer nanocomposite. To achieve this goal, we modified raw sericite by thermal modification, acid activation, and sodium modification. The modified sericite was then co-intercalated by cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and anionic surfactant sodium dodecyl sulfate (SDS). The intercalated sericite was characterized by XRD, FTIR, SEM, DTA-TG, and a contact angle tester. The optimized sample had a layer-to-layer distance of 6.56 nm and an intercalation rate of 95.7%. Compared with raw sericite, the new organo-sericite showed increased hydrophobicity. A proposed mechanism for the intercalation by these surfactants was also discussed. Finally, sericite/epoxy composite was prepared by using the new organo-sericite as the raw material, demonstrating significantly improved mechanical properties compared to pure epoxy resin (72% improved for bending strength and 62% improved for tensile strength, compared with pure epoxy resin). The new organo-sericite is a promising filler in epoxy resin to enhance thermal stability and mechanical performance of the composite. Full article

Natural zeolites are highly effective adsorbents that can remove various metal cations which would otherwise contaminate the environment. However, different metal cations (Cu, Zn, and Ag) within their lattice or quaternary long-chain surfactant cations on their surface modify their affinity towards hazardous anions and promote antibacterial activity in natural zeolites. Specifically, natural zeolites in their non-modified form lack intrinsic antibacterial characteristics. NZ is the most widespread natural zeolite. This review presents the antibacterial efficiency of NZ containing transition metals, nano oxides, and organics. This effect is nonspecific and primarily driven by the nutritional makeup of the medium rather than the species of pathogenic bacteria under study. Studies on using NZ-based disinfectants to clean up contaminated water and soil and using modified and purified NZ to protect health are also considered. By eliminating toxic ions and, when modified by these toxic cations, removing pathogens from the environment, natural NZ can serve a dual function, providing it with the distinctive characteristics of a sustainable material. Full article

Surfactants are often used in the process of coal dust suppression, and the wetting effect is greatly affected by the surfactant hydrophilic group structures. In order to explore the influence of hydrophilic groups of surfactants on their adsorption states and wetting effect on coal dust, three surfactants with similar hydrophilic groups were selected, namely, anionic surfactant sodium dodecyl sulfate (SDS), anionic-nonionic surfactant alkyl ether sulfate (AES), and nonionic surfactant alkyl polyoxyethylene ether-3 (AEO-3). To assess surfactant efficiency, surface tension, wetting time, infrared spectra, and wetting heat were analyzed. These parameters provide insights into molecular adsorption, interfacial behavior, and energy changes during wetting. The different adsorption states of surfactants on the coal dust surface due to EO and SO₄²⁻ hydrophilic groups were analyzed. Results show that both anionic surfactant SDS and nonionic surfactant AEO-3 form the monolayer adsorption structure on the coal dust surface. Due to the electrostatic repulsion of SO₄²⁻ groups, the adsorption density of SDS is lower than that of AEO-3, which results in the higher wetting heat of AEO-3 compared to SDS. In addition, the EO groups without electrostatic repulsion make AEO-3 molecules more tightly adsorbed at the air–liquid interface, causing the minimal surface tension. Therefore, the wetting time of AEO-3 is shorter than that of SDS. The anionic-nonionic surfactant AES has both EO and SO₄²⁻ groups. Because the EO groups in the inner surfactant adsorption layer can attract Na⁺ ions to distribute around them, the free AES molecules further form the outer adsorption layer under the electrostatic attraction between SO₄²⁻ groups and Na⁺ ions. The double-layer adsorption structure causes the hydrophobic groups of the outer AES molecules to face outward, the hydrophobic sites on the coal dust surface are not completely transformed into hydrophilic sites. Although AES exhibits the highest adsorption density, it has the lowest wetting heat and the longest wetting time. The research results can provide theoretical guidance for the selection of suitable surfactants for coal dust suppression. Full article

The performance of oil–water coalescence separation elements currently fails to meet the increasing demands of the oily wastewater treatment industry. To address this challenge, a series of fiber coalescing filters were developed through an underwater superoleophobic modification process using a simple impregnation technique. The effect of varying surface wettability on the separation efficiency of oil-in-water (O/W) emulsions stabilized with surfactants was investigated. The results demonstrate that, after undergoing underwater superoleophobic modification, the separation efficiency of the fiber filter material improved by 33.9%, the pressure drop was reduced by 46.1%, and the steady-state quality factor increased by 83.3%. Building upon these findings, an oil-repellent pore size gradient structure was introduced for the coalescence separation of surfactant-stabilized oil-in-water emulsions. This structure exhibited outstanding characteristics, including a low pressure drop and a high-quality factor. Furthermore, when processing emulsions stabilized with surfactants such as OP-10 (nonionic), CTAB (cationic), and SDS (anionic), the structure maintained high separation efficiencies of 93.6%, 96.4%, and 97.2%, respectively, after 10 cycles. Finally, based on experimental data and theoretical analysis, a separation mechanism for oil–water coalescence using superoleophobic pore size gradient filtration materials is proposed. This structure demonstrates significant potential for widespread application in liquid–liquid separation technologies. Full article

Antimicrobial resistance (AMR) is a global health threat, with methicillin-resistant Staphylococcus aureus (MRSA) being one of the major resistant pathogens. This study reports the isolation of a novel mangrove-derived bacterium, Virgibacillus chiguensis FN33, as identified through genome analysis and the discovery of a new anionic antimicrobial peptide (AMP) exhibiting anti-MRSA activity. The AMP was composed of 23 amino acids, which were elucidated as NH₃-Glu-Gly-Gly-Cys-Gly-Val-Asp-Thr-Trp-Gly-Cys-Leu-Thr-Pro-Cys-His-Cys-Asp-Leu-Phe-Cys-Thr-Thr-COOH. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) for MRSA were 8 µg/mL and 16 µg/mL, respectively. FN33 AMP induced cell membrane permeabilization, suggesting a membrane-disrupting mechanism. The AMP remained stable at 30–40 °C but lost activity at higher temperatures and following exposure to proteases, surfactants, and extreme pH. All-atom molecular dynamics simulations showed that the AMP adopts a β-sheet structure upon membrane interaction. These findings suggest that Virgibacillus chiguensis FN33 is a promising source of novel antibacterial agents against MRSA, supporting alternative strategies for drug-resistant infections. Full article