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Wildfires affect soils in multiple ways, leading to numerous challenges for colonizing microorganisms. Although it is thought that fire-adapted microorganisms lie at the forefront of postfire ecosystem recovery, the specific strategies that these organisms use to thrive in burned soils remain largely unknown. Through bioactivity screening of bacterial isolates from burned soils, we discovered that several Paraburkholderia spp. isolates produced a set of unusual rhamnolipid surfactants with a natural methyl ester modification. These rhamnolipid methyl esters (RLMEs) exhibited enhanced antimicrobial activity against other postfire microbial isolates, including pyrophilous Pyronema fungi and Amycolatopsis bacteria, compared to the typical rhamnolipids made by organisms such as Pseudomonas spp. RLMEs also showed enhanced surfactant properties and facilitated bacterial motility on agar surfaces. In vitro assays further demonstrated that RLMEs improved aqueous solubilization of polycyclic aromatic hydrocarbons, which are potential carbon sources found in char. Identification of the rhamnolipid biosynthesis genes in the postfire isolate, Paraburkholderia kirstenboschensis str. F3, led to the discovery of rhlM, whose gene product is responsible for the unique methylation of rhamnolipid substrates. RhlM is the first characterized bacterial representative of a large class of integral membrane methyltransferases that are widespread in bacteria. These results indicate multiple roles for RLMEs in the postfire lifestyle of Paraburkholderia isolates, including enhanced dispersal, solubilization of potential nutrients, and inhibition of competitors. Our findings shed new light on the chemical adaptations that bacteria employ to navigate, grow, and outcompete other soil community members in postfire environments.

Azoarene isomerization lies at the heart of numerous applications, from catalysis or energy storage to photopharmacology. While efficient switching between their E and Z isomers predominantly relies on UV light, a recent study by Klajn and co‐workers introduced visible light sensitization of E azoarenes and their subsequent isomerization as a tool coined disequilibration by sensitization under confinement (DESC) to obtain high yields of the Z isomer. This host–guest approach is, however, still constrained to minimally substituted azoarenes with limited applicability in advanced molecular systems. Herein, we expand DESC for the assembly of surfactants at the air–water interface. Leveraging our expertise with photoswitchable amphiphiles, we induce substantial alterations of the water surface tension through reversible arylazopyrazole isomerization. After studying the binding of charged surfactants to the host, we find that the surface activity differences upon visible light switching for both isomers are comparable to those obtained by UV light excitation. The method is demonstrated on a large concentration range and can be activated using green or red light, depending on the sensitizer chosen. The straightforward implementation of photoswitch sensitization in a complex molecular network showcases how DESC enables the improvement of existing systems and the development of novel applications driven by visible light. [ABSTRACT FROM AUTHOR]

Hypothesis Atomistically-detailed models of surfactants provide quantitative information on the molecular interactions and spatial distributions at fluid interfaces. Hence, it should be possible to extract from this information, macroscopical thermophysical properties such as interfacial tension, critical micelle concentrations and the relationship between these properties and the bulk fluid surfactant concentrations. Simulations and Experiments Molecular-scale interfacial of systems containing n- dodecyl β -glucoside (APG 12) are simulated using classical molecular dynamics. The bulk phases and the corresponding interfacial regions are all explicitly detailed using an all-atom force field (PCFF+). During the simulation, the behaviour of the interface is analyzed geometrically to obtain an approximated value of the critical micelle concentration (CMC) in terms of the surfactant area number density and the interfacial tension is assessed through the analysis of the forces amongst molecules. New experimental determinations are reported for the surface tension of APG 12 at the water/air and at the water/ n -decane interfaces. Findings We showcase the application of a thermodynamic framework that inter-relates interfacial tensions, surface densities, CMCs and bulk surfactant concentrations, which allows the in silico quantitative prediction of interfacial tension isotherms. • We present a method to relate molecular observations to interfacial tensions. • Atomistic simulation results are provided for n -dodecyl β -glucoside; (APG 12). • New experimental determinations are reported for the water/air and water/ n -decane interfacial tension. • Consistency is seen between simulations, experiments and machine learning predictions. [ABSTRACT FROM AUTHOR]

There is a substantial body of literature exploring the challenges associated with exploring and exploiting these underground resources. Unconventional resources, particularly heavy oil reservoirs, are critical for meeting ever-increasing global energy demand. By injecting surfactants into heavy oil, chemically enhanced oil recovery (EOR) may enable emulsification, which may reduce the viscosity of heavy oil and facilitate extraction and transportation. In this work, a large experimental dataset, containing 2020 data points, was extracted from the literature for modeling oil-in-water (O/W) emulsion viscosity using machine learning (ML) methods. The algorithms used pressure, temperature, salinity, surfactant concentration, type of surfactant, shear rate, and crude oil density as inputs. For this purpose, five ML algorithms were selected and optimized, including adaptive boosting (AB), convolutional neural network (CNN), ensemble learning (EL), artificial neural network (ANN), and decision tree (DT). A combined simulated annealing (CSA) method was utilized to optimize all algorithms. With AARE, R2, MAE, MSE, and RMSE values of 8.982, 0.996, 0.004, 0.0002, and 0.0132, respectively, the ANN predictor exhibited higher accuracy in predicting O/W emulsion viscosity for total data (train and test subsets combined). A Monte-Carlo sensitivity analysis was also performed to determine the impact of input features on the model output. By using the proposed ML predictor, expensive and time-consuming experiments can be eliminated and emulsion viscosity predictions can be expedited without the need for costly experiment. [ABSTRACT FROM AUTHOR]

To solve the severe coal dust pollution and dust hazards in underground coal mines, this study utilized graft copolymerization modification technology and compound technology to develop a mining composite consolidation dust suppressant. On this basis, analysis of its consolidation wettability and dust suppression mechanism was conducted through characterization tests and molecular dynamics simulation methods. The results show that polyacrylamide (PAM) had been successfully grafted onto the soybean protein isolate (SPI) molecule, and form a SPI‐PAM complex. After the dust suppressant acted on the coal dust surface, it utilized its wealthy hydrophilic groups, for the adsorption of water molecules and the positive amide group for binding to produce a large area of agglomeration of coal dust particles at the interface, exhibiting good wetting and consolidation into a shell. At the same time, molecular dynamic simulation verified that the diffusivity of water molecules in the dust suppressant‐coal system was 0.30Å2/ps, decreased by 43.3%, and the interaction energy with coal molecules was −200.27 kcal/mol, absolute value increased by 41.35%, which made the dust suppressant molecules more easily adsorb and agglomerate on the surface, demonstrated an excellent solidification and dust suppression effect. [ABSTRACT FROM AUTHOR]

Bubble coalescence plays a critical role in optimizing biological and industrial processes, impacting efficiency in areas such as fermentation, wastewater treatment, and foaming control. While the relationship between chemical structure and bubble coalescence has been thoroughly explored for inorganic ions, limited data exist on organic ions and surfactants, despite their widespread use in these industries. This study addresses this gap by investigating the effects of surfactant hydrophobicity and bubble size on coalescence behavior at a flat air–liquid interface and within a bubble column. Surface tension measurements were employed to assess surfactant hydrophobicity, while bubble size and coalescence time were analyzed to determine their respective influences. The results reveal a novel quantitative relationship between surfactant hydrophobicity and the half-coalescence inhibition concentration (HCIC), a new variable introduced in this study. This relationship demonstrates that as hydrophobicity increases, the HCIC also rises, providing a new relationship between surfactant hydrophobicity and bubble coalescence. While it is well-known that more hydrophobic molecules delay coalescence, this is the first time a direct, proportional relationship has been established with HCIC, offering a new parameter for predicting and controlling coalescence phenomena. [ABSTRACT FROM AUTHOR]

This work presents the results of a study on the effect of ionic surfactants: cationic hexadecyltriammonium bromide (CTAB) and anionic sodium salt of sulfonic acid (1OSASS) on the Bi(III) electroreduction process in mixed aqueous–organic supporting electrolyte solutions containing methanol. This study showed that the composition of the supporting electrolyte solution, particularly the methanol and surfactant concentrations, significantly affects the mechanism and rate of the Bi(III) ion electroreduction. Analysis of the influence of the indicated factors on the mechanisms and kinetics of metal ion electroreduction can contribute not only to the optimization of industrial electrochemical processes but also to the development of innovative technological solutions, such as advanced electrochemical materials and novel sensors. In these experiments, an innovative electrode made of cyclic renewable liquid silver amalgam (R-AgLAFE) was used as a working electrode, which stands out among classic mercury electrodes (HMDE type) due to the significant reduction in mercury consumption while maintaining similar performance. [ABSTRACT FROM AUTHOR]

In this brief review, we have discussed various physical chemical principles that guide the functions of surfactants in solution. The surfactants have special functions at the air/liquid and air/solid interfaces forming Gibbs and Langmuir monomolecular films by way of spreading at the interfaces. Their self‐aggregation or micelle formation, a remarkable and useful phenomenon has been presented and elaborated. The application of fundamental physical chemistry principles for the understanding of the energetics of the micelle formation has been discussed. The involvement of surfactants in the formation of soft assembled (condensed) matters namely, vesicles, emulsions, foams, reverse micelles (or, microemulsions), gels, and so forth has been presented. The uniqueness of the "critical micelle concentration" (CMC), and its determination have been briefly presented. Applications of surfactants are numerous. We have briefly cited several applications namely, nano‐material synthesis, detergency, agrochemical formulations, drug delivery, retardation of water evaporation, and so forth. A short account of bio‐related surfactants namely, lung surfactants, bile salts, plant‐and microbe‐generated bio‐surfactants, and their utilities have been also presented. [ABSTRACT FROM AUTHOR]

As the single largest class of specialty chemicals, surfactants are consumed in huge quantities in our daily life and in many industrial areas. In the past, the attention was focused entirely on technical performance. However, starting from the 1970s and 80s, surfactant related environmental concerns have become the main driving force to upgrade surfactant production technology to make more benign or "greener" products. For this reason, environmental issues, dermatological effects, and oral toxicity are the main priorities when surfactants are considered for a specific purpose. In this paper, we present five cases to demonstrate how the surfactant industry tackles these challenges to mitigate the environmental and health effects associated with surfactant consumption. We also discuss the important role played by surfactants in a current carbon capture and storage (CCS) strategy to reduce the CO2 level in the atmosphere. Surfactant-based stable CO2 foam flooding is a well-established enhanced oil recovery technique. It has been considered to be an economically realistic procedure to sequester large amounts of CO2 in geological formations. [ABSTRACT FROM AUTHOR]

The permeability of ore is a key factor affecting the leaching effect of uranium ore, and the addition of surfactants can significantly improve the permeability of ore, thereby strengthening uranium ore leaching. This article simulates two infiltration leaching processes, atmospheric heap leaching and pressurized in-situ leaching, and explores the effect of surfactant cetyltrimethylammonium bromide on uranium leaching rate and ore permeability coefficient in both processes. The results showed that in the atmospheric heap leaching test, adding surfactants increased the ore leaching rate by 30.31% during the same 13 day test cycle, and the leaching process was mainly controlled by surface chemical reactions. In the pressurized in-situ leaching test, based on the results of a leaching cycle of 13 days, the average permeability coefficient increased by 72.89% and 64.07% after adding surfactants to the drained and water containing uranium deposits, respectively. In addition, the peak uranium concentration in the leaching solution appeared 2 days earlier, indicating that the addition of surfactants has a significant promoting effect on in-situ leaching of uranium, improving the leaching efficiency of uranium, and can improve the leaching rate of uranium within the same leaching cycle. [ABSTRACT FROM AUTHOR]

Perfluorooctanoic acid (PFOA) is a surfactant that is detected in small quantities across various environments away from its manufacturing zones. Despite the widespread detection of PFOA in aquatic ecosystems, the impact of this compound on phytoplankton populations remains poorly understood. This study aimed to determine the physiological effects of PFOA on Microcystis aeruginosa. The cyanobacterium was exposed to 1‒10 000 μg l‒1 PFOA for 7 days under controlled laboratory conditions. The EC50 of PFOA for the test species after 7 days of exposure was 30.03 μg l‒1. Cell density significantly decreased at all PFOA concentrations (1‒10 000 μg l‒1). Chlorophyll a and carotenoid concentrations increased on day 1 (except for 1 μg l‒1, the lowest PFOA treatment) but then decreased across all treatment concentrations on day 7 of the experiment. When M. aeruginosa was exposed to PFOA, the total lipid, protein and carbohydrate content generally increased across all treatment concentrations. The concentration of intracellular hydrogen peroxide increased with increasing surfactant concentrations. In different treatments, lipid peroxidation increased, with 100 μg l‒1 PFOA producing the highest malondialdehyde content. Peroxidase and glutathione S-transferase activities increased across all treatment concentrations, demonstrating progressive changes consistent with the increase in reactive oxygen species observed. Total microcystin concentration increased in cultures exposed to 1000 and 10 000 µg l‒1 PFOA. These findings suggest that PFOA can adversely affect the survival of M. aeruginosa populations in contaminated aquatic ecosystems, with potential cascading effects on the general health of the environment. [ABSTRACT FROM AUTHOR]

In this study, a new method was introduced to induce micellar transitions by using vesicles formed from mixed surfactants, which offer enhanced stability. Different physicochemical analysis methods were used to study the transition mechanism and the aggregation behavior of the mixed aqueous system composed of the double‐chain cationic didodecyldimethylammonium bromide (DDAB) and a single‐chain nonionic fluorinated surfactant undecafluoro n‐pentyl decaoxyethylene ether (C5F11(EO)10), by varying the fraction of DDAB, then the total surfactant concentration of DDAB/C5F11(EO)10 mixed system at XDDAB = 0.9. The obtained results indicated that the addition of the fluorinated surfactant C5F11(EO)10 to the mixed system resulted in a reduction of the surface tension (γ) and a decrease in the Electrical conductivity (K). Furthermore, even at high total concentrations of the mixed system, the conductivity and charge density at the surface remained stable. As XDDAB values increased, a higher degree of dissociation (α) was observed, along with negative values in the thermodynamic parameters of micellization (ΔGCMC°$$ {G}_{\mathrm{CMC}}^{{}^{\circ}} $$, ΔGCVC°$$ {G}_{\mathrm{CVC}}^{{}^{\circ}} $$, and ΔGads°$$ {G}_{\mathrm{ads}}^{{}^{\circ}} $$), confirming the transition from micelles to vesicles. The dynamic light scattering (DLS) analysis revealed the formation of two stable types of aggregates at both low and high concentrations, as supported by the zeta potential (ζ). Upon increasing the concentration of surfactants, UV–Vis absorption measurements indicated that small spherical micelles grow into large multilamellar vesicles, as evidenced by an increase in turbidity and confirmed transmission electron microscopy images. [ABSTRACT FROM AUTHOR]

Surfactant monolayers modify the surface tension of fluid surfaces, and they confer to the surfaces a resistance to mechanical perturbances, such as compression or dilatation. The resistance can be characterized by elastic and viscous moduli, that affect the phenomena involving the motion of liquid surfaces such as wetting, two‐phase flow, foaming and emulsification, rheology and stability of foams and emulsions. Some of these phenomena, for instance coalescence of bubbles or drops, are extremely rapid, and although coalescence seems correlated with the elastic compression modulus, no quantitative comparison has been made. Indeed, this modulus is frequency dependent, and cannot be measured by most conventional devices at the short timescales during which coalescence events occur. In this paper, we first review the current understanding on foam and emulsion stability, highlighting the role of surface rheology in the stability of these systems, important for their formulation. We present tension measurements for various surfactant systems, nonionic and cationic, at oil–water interfaces. We show calculations of the high frequency elastic modulus using the Gibbs adsorption equation and compare the results to previous measurements at air–water interfaces. The moduli measured imposing a rapid expansion of the monolayers are consistently smaller, in particular at oil–water interfaces. We discuss the possible origin of the differences between the two types of interfaces. [ABSTRACT FROM AUTHOR]

Superalloys, specifically Inconel 617 (IN617), have distinctive properties, yet it is extremely hard to machine through traditional processes. Electric discharge machining (EDM) has been considered a viable option considering the characteristics and shape intricacy required in the applications of the said alloy. However, EDM's low material removal rate (MRR) impedes its use. Therefore, the machining performance of five different transformer oil (TO) based modified dielectrics and cryogenically treated (CT) tools have been thoroughly investigated herein, which has never been examined so far. A total of 30 experiments were executed employing a full factorial design considering three kinds of electrodes and five different modified dielectrics. CT Cu (CuCT) electrode has given the highest magnitude of MRR (19.65 mm3/min) in the blend of tween 80 and TO, and minimum surface roughness (Rz) 11.0 µm in pure TO. The maximum MRR obtained with the CT electrode is 28% greater in comparison to that recorded for non-treated (NT) electrodes. Among the different electrodes, the CuCT tool performed well in TO-based dielectrics by giving the high MRR compared to the other NT and CT electrodes. CT electrodes yield higher MRR in TO-based dielectrics than kerosene oil (KO) based ones. The highest value of MRR noticed with TO-based dielectric is 20.3% than the maximum MRR noted for the KO-based dielectric. A significant amount of improvement in the MRR (98.56%) and Rz (78.88%) has been observed when the mono-objective optimization is utilized to obtain the optimal set of input variables. Finally, an artificial neural network (ANN) has been modelled to accurately forecast the MRR and Rz value for various input conditions, obviating the necessity for tests, effectively modelling the complicated and nonlinear phenomenon of MRR and Rz. [ABSTRACT FROM AUTHOR]

The present work aimed to evaluate whether the use of an innovative method such as hydrodynamic cavitation (HC) is suitable for the simultaneous removal of surfactants of different chemical natures (non-ionic, anionic and cationic) from actual car wash wastewater at different numbers of passes through the cavitation zone and different inlet pressures. An additional novelty was the use of multi-criteria decision support, which enabled the selection of optimal HC conditions that maximized the removal of each group of surfactants and chemical oxygen demand (COD) with minimal energy input. For the optimal HC variants, Fourier transform infrared spectroscopy (FT-IR/ATR) as well as investigations of surface tension, zeta potential, specific conductivity, system viscosity and particle size were carried out. The highest reduction of non-ionic surfactants was found at 5 bar inlet pressure and reached 35.5% after 120 min. The most favourable inlet pressure for the removal of anionic surfactants was 3 bar and the removal efficiency was 77.2% after 120 min, whereas the most favourable inlet pressure for cationic surfactant removal was 3 bar, with the highest removal of 20% after 120 min. The obtained results clearly demonstrate that HC may constitute an effective, fast and cost-efficient method for removing surfactants from real industrial wastewater. [ABSTRACT FROM AUTHOR]

The chemical enhanced oil recovery (cEOR) uses substances to improve the mobility of petroleum in reservoirs. Among these substances are the surfactants, whose purpose is to change the wettability and interfacial tension (IFT). We focus on experiments of surfactants in rocks from Chicontepec Paleochannel. CTAB, DTAB and SDS surfactants in brines of NaCl and KCl and mineral oil were investigated for reduction of IFT and contact angle alteration. The sessile and pendant drop methods were used to determine the IFT. The electrical affinity of the rock surface, dissolved ions, and the surfactant molecules, play key roles in the alteration of wettability and IFT. Thus, one scheme of interactions between the electrical charges is proposed on the basis of the rocky characterization and the following results: the lowest contact angle was 106° with CTAB at 0.01 wt% in brines at 9.25 g/L NaCl, and 108° with SDS at 0.01 wt% in brines at 20 g/L NaCl. The smallest IFT was 0.813 dyn/cm with CTAB at 0.5 wt% in brines at 5 g/L KCl. This work serves as first assessments of these surfactants to enhance the production in Chicontepec, employing cheap tensoactives to increase the applicability. Besides, these results will guide future displacement tests as cEOR lab simulation. [ABSTRACT FROM AUTHOR]

Comprehensive Summary Oil‐in‐oil nonaqueous emulsions are of great interest for developing emulsion‐templated polymers and encapsulation systems that are incompatible with water‐sensitive substances. Tailor‐made amphiphilic block copolymers are by far the most efficient stabilizers for oil‐in‐oil emulsions while less attention is given to copolymers with more complex architectures. Here, we report the stabilization of DMSO‐silicone oil interface by bottlebrush random copolymers (BRCPs) containing norbornene backbones with densely grafted poly(methyl methacrylate) (PMMA) and polystyrene (PS) side chains. The assembly kinetics of BRCPs at the DMSO‐silicone oil interface can be divided into three processes, including diffusion, reconfiguration and reorganization, and can be varied by tuning the degree of polymerization of the backbone (NB). Due to the high efficiency of BRCPs in reducing the interfacial tension, when using BRCPs as stabilizers, stable silicone oil‐in‐DMSO traditional emulsions and high internal phase emulsions (HIPEs) can be successfully obtained, while no stable emulsions can be achieved with linear PMMA‐b‐PS serving as the stabilizer. This study, for the first time, underscores the great potential of amphiphilic bottlebrush copolymers in preparing oil‐in‐oil emulsions. Given the advances in polymerization strategy, a broad variety of amphiphilic bottlebrush copolymers are expected to be synthesized and applied in the stabilization of nonaqueous biphasic systems. [ABSTRACT FROM AUTHOR]

Microemulsion based fuels (MBF) have gained significant attention in recent years due to their potential to enhance combustion efficiency, reduce emissions, and improve overall engine performance. This research paper enlightens the effects of physiochemical properties on the emission characteristics of CI engine. The microemulsions are formulated using surfactants, co‐surfactants, water or alcohols, and fuel components. The effects of density, viscosity, calorific value, cold flow properties, and cetane number along with the stability and the multi‐component characteristics of (MBF) has been taken into consideration to examine its effects on Emission characteristics such as nitrogen oxides (NOx), sulfur oxides (SOx), carbon monoxide (CO), particulate matter (PM), and unburned hydrocarbons (UHC). Microemulsion‐based fuels lower emissions of NOx and PM, recognized to the more complete combustion. The review highlights various studies that have investigated the benefits of microemulsion fuels, including reduced emissions of different pollutants and thus reduce the adverse effect on environment. In conclusion, microemulsion‐based fuels show likely physiochemical properties, as well as favorable emission characteristics, with reduced NOx, SOx, CO, PM, and UHC emissions. This study highlights the potential of microemulsion‐based fuels as environment friendly alternatives, flagging the way for further research. [ABSTRACT FROM AUTHOR]

Nano- and micro-sized vesicular and colloidal structures mediate cell–cell communication. They are important players in the physiology of plants, animals, and humans, and are a subject of increasing interest. We investigated the effect of three surfactants, N-cetylpyridinium chloride (CPC), sodium dodecyl sulfate (SDS), and Triton X-100 (TX100), and two anionic polyelectrolytes, sodium polystyrene sulfonate (NaPSS) and sodium polymethacrylate (NaPMA), on nanoliposomes. In addition, the effect of SDS and TX100 on selected biological membranes (erythrocytes and microalgae) was investigated. The liposomes were produced by extrusion and evaluated by microcalorimetry and light scattering, based on the total intensity of the scattered light (Itot), hydrodynamic radius (Rh), radius of gyration (Rg), shape parameter p (=Rh/Rg,0), and polydispersity index. The EPs shed from erythrocytes and microalgae Dunaliella tertiolecta and Phaeodactylum tricornutum were visualized by scanning electron microscopy (SEM) and analyzed by flow cytometry (FCM). The Rh and Itot values in POPC liposome suspensions with added CPC, SDS, and TX100 were roughly constant up to the respective critical micelle concentrations (CMCs) of the surfactants. At higher compound concentrations, Itot dropped towards zero, whereas Rh increased to values higher than in pure POPC suspensions (Rh ≈ 60–70 nm), indicating the disintegration of liposomes and formation of larger particles, i.e., various POPC–S aggregates. Nanoliposomes were stable upon the addition of NaPSS and NaPMA, as indicated by the constant Rh and Itot values. The interaction of CPC, SDS, or TX100 with liposomes was exothermic, while there were no measurable heat effects with NaPSS or NaPMA. The SDS and TX100 increased the number density of EPs several-fold in erythrocyte suspensions and up to 30-fold in the conditioned media of Dunaliella tertiolecta at the expense of the number density of cells, which decreased to less than 5% in erythrocytes and several-fold in Dunaliella tertiolecta. The SDS and TX100 did not affect the number density of the microalgae Phaeodactylum tricornutum, while the number density of EPs was lower in the conditioned media than in the control, but increased several-fold in a concentration-dependent manner. Our results indicate that amphiphilic molecules need to be organized in nanosized particles to match the local curvature of the membrane for facilitated uptake. To pursue this hypothesis, other surfactants and biological membranes should be studied in the future for more general conclusions. [ABSTRACT FROM AUTHOR]

In this study, we demonstrate the electrodeposition of copper nanoparticles (NPs) on pencil graphite electrodes (PGEs) utilizing sodium dodecyl sulphate (SDS) as a soft template. The utilization of the surfactant had an impact on both the physical arrangement and electrochemical characteristics of the modified electrodes. The prepared Cu-SDS/PGE electrodes had hierarchical dendritic structures of copper NPs, thereby increasing the surface area and electrochemical catalytic activity in comparison with Cu/PGE electrodes. The Cu-SDS/PGE electrode showed excellent catalytic activity in reducing hydrogen peroxide, resulting in the sensitive and selective detection of hydrogen peroxide. The electrode exhibited a good sensitivity of 21.42 µA/µM/cm2, a lower limit of detection 0.35, and a response time of less than 2 s over a wide range spanning 1 µM to 1 mM of hydrogen peroxide concentrations. The electrodes were also highly selective for H2O2 with minimal interference from other analytes even at concentrations higher than that of H2O2. The approach offers the benefit of electrode preparation in just 5 min, followed by analysis in 10 min, and enables for the quantitative determination of hydrogen peroxide within 30 min. This can be achieved utilizing a newly prepared, cost-effective electrode without the need for complex procedures. [ABSTRACT FROM AUTHOR]

The removal of caesium radionuclides from an aqueous solution by flotation using rice straw (RS) agricultural waste as a low-cost and eco-friendly adsorbent in the presence of potassium ferrocyanide (KFC) was investigated. The influence of many adsorption parameters and flotation was evaluated on the removal efficiency of 137Cs. The adsorption results demonstrated that the concerned radionuclide was efficiently removed in the presence of 2 × 10−4 mol/L KFC using 10 g/L RS at pH ≥ 7. The double exponential kinetic model and the Freundlich model were the best models for fitting the adsorption kinetic and isotherm data, respectively. The maximum adsorption capacity of RS, calculated from the Langmuir model, was 280.405 mg/g. after being transferred to the flotation cell, 137Cs loaded onto ferrocyanide-modified rice straw (FMRS) was successfully floated at pH 7 using 3 × 10−4 mol/L cetyltrimethylammonium bromide (CTAB) surfactant in the presence of 4% ethanol. Removal percentages of 56% and > 99.5% were achieved for 137Cs-loaded FMRS within 5 min using sodium dodecyl sulphate (SDS) and CTAB, respectively. The results obtained in this investigation indicate the efficiency of the suggested strategy and hence its applicability for the removal of 137Cs+ from radioactive liquid wastes. [ABSTRACT FROM AUTHOR]

Polar organic chemical integrative samplers (POCIS) are promising devices for measuring the time‐weighted average concentrations of hydrophilic compounds in aquatic environments. However, the mechanisms underlying compound uptake by POCIS remain unclear. We investigated the permeation kinetics of polyethersulfone and polytetrafluoroethylene membrane filters, and the sorption kinetics of Oasis HLB (Waters), Envi‐Carb (Supelco), and Oasis WAX (Waters) sorbents. The log octanol−water partition coefficient (KOW) values of the 19 targeted compounds ranged from −0.55 to 6.0. The overall mass‐transfer coefficients were negatively correlated with KOW, indicating that interactions between hydrophobic compounds and the membrane inhibit permeation. The sorption rate coefficient showed no correlation with KOW and depended on the type of sorbent used. These results imply that the uptake of highly hydrophilic compounds by POCIS is determined by both the membrane and the sorbent kinetics; however, membrane kinetics dominate the uptake of hydrophobic compounds. Environ Toxicol Chem 2024;43:2115–2121. © 2024 SETAC [ABSTRACT FROM AUTHOR]

Stainless steel in the industry has many wide-ranging applications, but in some harsh conditions, there is still the possibility of corrosion, and the use of corrosion inhibitors is an economical and effective way to prevent corrosion. In this study, an investigation was conducted on the impact of surfactant hydrocarbon chain length on the corrosion inhibition in 0.5 M sulfuric acid (H2SO4) solution for 304 stainless steel (304SS) using 1 mM alkyl trimethyl ammonium bromide (CnTAB) with varying hydrocarbon chain lengths (from 6 to 18). The inhibition efficiency (IE%) was assessed by loss-in-weight method, electrochemical measurements, and surface analysis. Additionally, the corrosion inhibition mechanism was explored conjunction with quantum chemical calculations. The findings show that these corrosion inhibitors effectively protect 304SS, with the inhibition effect being correlated to hydrocarbon chain length. The corrosion inhibitors exhibit an enhancement in inhibition efficiency with an increase in the length of the hydrocarbon chain, peaking at C16 (weight loss 96.3%, electrochemical results > 72%), but subsequently decreases as the chain length reaches C18. Furthermore, the results of the trials show that the CnTAB's adsorption on the 304SS surface conforms to Langmuir isotherms, which is a hybrid corrosion inhibitor, and appropriate thermodynamic adsorption parameters were determined based on these characteristics. [ABSTRACT FROM AUTHOR]

Biosurfactants (BSs) are surface-active agents (surfactants) produced by microorganisms. In a broad sense, it is understood as surfactants produced by whole living organisms, but most of the surfactants used as BS in the world are fermented products. In recent years, global leading companies have entered the industrial field, increasing competition in the BS business. Additionally, there has been active BS research in the academic field. A group of researchers, mainly from Europe, have held the Biosurfactant International Conference since 2019 and recently opened Research Topics in Frontiers in Bioengineering and Biotechnology, where 15 papers have been published. In this article, we will outline the situation surrounding BSs and then introduce several selected topics. [ABSTRACT FROM AUTHOR]

The sol–gel process is a green method used in the last few decades to synthesize new organic–inorganic phosphorus-containing hybrid materials. The sol–gel synthesis is a green method because it takes place in mild conditions, mostly by using water or alcohol as solvents, at room temperature. Therefore, the sol–gel method is, among others, a promising route for obtaining metal-phosphonate networks. In addition to phosphorus, the obtained hybrid materials could also contain titanium, zirconium, boron, and other elements, which influence their properties. The sol–gel process has two steps: first, the sol formation, and second, the transition to the gel phase. In other words, the sol–gel process converts the precursors into a colloidal solution (sol), followed by obtaining a network (gel). By using the sol–gel method, different organic moieties could be introduced into an inorganic matrix, resulting in organic–inorganic hybrid structures (sometimes they are also referred as organic–inorganic copolymers). [ABSTRACT FROM AUTHOR]

For many decades, natural and modified clay minerals have been used as adsorbents to clean up aquatic and soil ecosystems contaminated with organic and inorganic pollutants. In this study, organoclays based on bentonite and various amphoteric and nonionic surfactants were synthesized and tested as effective sorbents for lead ions. The maximum values of R were obtained when describing the sorption processes using the Langmuir model, which ranged from 0.97 to 0.99. The adsorption of lead ions by these organoclays was investigated using different sorption models including the Langmuir, Freundlich, and BET. It was found that, according to the values of limiting adsorption to the Langmuir equation, the synthesized organoclays formed an increasing series: organoclay with cocamide diethanolamine < bentonite < organoclay with lauramine oxide < organoclay with sodium cocoiminodipropionate < organoclay with disodium cocoamphodiacetate < organoclay with alkyl polyglucoside. The Gibbs energy for all of the analyzed samples was calculated and found to be negative, indicating the spontaneity of the cation adsorption process in the forward direction. The maximum value of the adsorption capacity of lead cations on organoclay-based bentonite with alkyl polyglucoside was 1.49 ± 0.05 mmol/g according to the Langmuir model, and 0.523 ± 0.003 mmol/g as determined by the BET model. In the process of modifying bentonite, there was an increase in negative values of the zeta potential for organoclays compared to the initial mineral, which clearly enhanced their electrostatic interactions with the positively charged lead ions. It was hypothesized, based on the physicochemical principles, that exchange adsorption is the main mechanism for lead absorption. Based on chemical approaches, organoclays based on amphoteric surfactants absorb lead mainly through the mechanisms of electrostatic attraction, ion exchange, and complexation as well as the formation of insoluble precipitates. Organoclays based on nonionic surfactants, on the other hand, absorb lead through mechanisms of complexation (including chelation) and the formation of insoluble chemical precipitates. The comparison of isotherms from different models allows us to find the most accurate match between the model and the experimental data, and to better understand the nature of the processes involved. [ABSTRACT FROM AUTHOR]

Triton X-100 (TX-100) is a commonly used surfactant in the manufacture of biosensors. The factors limiting the use of TX-100 in biosensors are environmental concerns. In this study, the binary system of sodium dodecyl benzene sulfonate (SDBS) and fatty alcohol-polyoxyethlene ether (AEO) was investigated from the physicochemical principle of surfactant interaction and its application in biosensors. The results demonstrated that a mixture of SDBS and AEO at an appropriate molar ratio had a comparable activity to TX-100 in terms of surface activity, micelle formation, dynamic adsorption, foaming, emulsifying, and cell permeability. Theory and experimentation support the idea that SDBS-AEO might take the place of TX-100 in the manufacturing of biosensors. This study contributes to the development of alternatives to TX-100 and provides a new perspective for an in-depth study of the interaction mechanism of additives in biosensor design. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) and their derivatives received more and more attention due to the diverse morphologies, rich porous structures, and tunable metal active sites, which have been widely used in energy-related electrocatalytic reactions. Surfactants, a class of compounds with hydrophilic and hydrophobic portions in the molecular structure, are able to modulate the properties of liquid and solid surfaces. Surfactants play a crucial role in controlling the shape and size of MOFs, which helps optimize electrocatalytic performance, especially in improving the exposure and accessibility of catalytic active sites. In this review, we first outline the types and applications of surfactants. Second, we describe the interface modulation and reaction mechanism of different surfactants during the forming of MOFs and their derivatives. Finally, we discuss the current applications of surfactant-modified MOFs and their derivatives in electrocatalysis. This review provides a better understanding of surfactant-assistant structure regulation and electrocatalytic activity study of MOFs and their derivatives. [ABSTRACT FROM AUTHOR]

For agricultural countries in Aisa, rice straw is a waste product, but also a valuable bioresource, with its recycling methods often drawing widespread attention. In this study, a novel multicomponent extraction method was proposed to perform comprehensive extraction of holocellulose and lignin from rice straw powder (RSP), resulting in modified rice straw powder (MRSP) with different micro‐morphologyies. The results indicate that the cosolvent tetraethylammonium chloride (TEAC) is more effective for extracting holocellulose and lignin compared to others, and different surfactants have decisive impacts on the extraction of holocellulose and lignin from RSP. Among them, anionic surfactants aid in the extraction of holocellulose, with sodium allylate sulfonate (SAS) being superior due to its greater changes in allyl polarity. Conversely, cationic surfactants facilitate the extraction of lignin, with octadearyl trimethyl ammonium chloride (OTAC) being superior due to the length of its alkyl‐carbon chain. And the quantized contribution of hydrophilic and hydrophobic groups of surfactants to the extraction of holocellulose and lignin, as well as, the different micromorphology of MRSP is obtained. Additionally, compared to the traditional PU (polyurethane) modified by eucalyptus wood powder (EWP/PU), the MRSP was used to prepare a series of biomass composite polyurethane synthetic leather (MRSP/PU), its tensile strength and peel strength of MRSP/PU coatings are greatly enhanced at the feedstock of 18 %. [ABSTRACT FROM AUTHOR]

The quest for scientifically advanced and sustainable solutions is driven by growing environmental and economic issues associated with coal mining, processing, and utilization. Consequently, within the coal industry, there is a growing recognition of the potential of microbial applications in fostering innovative technologies. Microbial-based coal solubilization, coal beneficiation, and coal dust suppression are green alternatives to traditional thermochemical and leaching technologies and better meet the need for ecologically sound and economically viable choices. Surfactant-mediated approaches have emerged as powerful tools for modeling, simulation, and optimization of coal-microbial systems and continue to gain prominence in clean coal fuel production, particularly in microbiological co-processing, conversion, and beneficiation. Surfactants (surface-active agents) are amphiphilic compounds that can reduce surface tension and enhance the solubility of hydrophobic molecules. A wide range of surfactant properties can be achieved by either directly influencing microbial growth factors, stimulants, and substrates or indirectly serving as frothers, collectors, and modifiers in the processing and utilization of coal. This review highlights the significant biotechnological potential of surfactants by providing a thorough overview of their involvement in coal biodegradation, bioprocessing, and biobeneficiation, acknowledging their importance as crucial steps in coal consumption. [ABSTRACT FROM AUTHOR]

The kinetics of hydrate formation in powder hydrogel systems saturated with aqueous surfactant solutions and stabilized with hydrophobic nanoparticles was studied. The systems were also studied for stability in multiple hydrate formation and dissociation cycles, i.e., for their capacity to maintain the original rate and degree of conversion of water to hydrate in the second and subsequent cycles. [ABSTRACT FROM AUTHOR]

Water scarcity, a challenge expected to worsen with climate change, significantly hinders native plant community restoration. Enhancing seed‐based restoration requires methods to increase the water availability for seeds and seedlings. Surfactants and superabsorbent polymers (SAPs) can improve soil water‐holding capacity and infiltration, but their use in seed enhancements remains underexplored. We investigated whether pellets containing surfactants or SAPs could improve seedling emergence of two native species (Rytidosperma caespitosum and Chrysocephalum apiculatum) common in temperate grasslands in south‐eastern Australia under different watering treatments. We used a randomized block design with five watering treatments to simulate predicted changes in precipitation for south‐eastern Australia: ambient, two reducing overall water volume, and two reducing watering frequency while increasing watering volume to maintain ambient treatment water volume. We explored four enhanced pellets (two containing surfactants and two containing SAPs) and non‐pelleted seeds. Our results showed that watering events with larger volumes but reduced frequency increased seedling emergence. Under these conditions, block co‐polymer surfactants further increased seedling emergence of C. apiculatum, while synthetic SAP pellets promoted emergence of R. caespitosum. Block co‐polymer surfactants decreased R. caespitosum emergence, and both SAPs reduced C. apiculatum emergence under reduced watering frequency. A 50% reduction in overall water volume significantly reduced seedling emergence for both species, regardless of seed enhancement. These findings suggest that surfactants and SAP pellets can improve the success of seed‐based restoration under ambient conditions and when rainfall events are larger in volume but reduced in frequency, but not when the overall volume of rainfall is reduced. [ABSTRACT FROM AUTHOR]

The Dynamic Light Scattering (DLS) measurements have been performed on quercetin with dioctyl sodium sulfosuccinate (Aerosol OT, AOT), Triton X-100 in 1,4-dioxane, as well as on the solutions containing water in the core of suitable reversed micelles; the water amount was calculated using the relation R = [H2O]/[surfactant], defining the ratio of water to surfactant concentration. The amount of quercetin in the studied systems as well as the effects of the water presence on the size of the micelles and diffusion effects were discussed. A significant effect of the research was the determination of the maximum amount of water that can be introduced into the AOT micelles in the studied systems. [ABSTRACT FROM AUTHOR]

As the complexity and the cost of infrastructures have risen, the need for a fast, reliable, cost-effective and clean fire extinguishing system has become important. Water mist is a clean and effective technology to deal with most types of fires. Over the years, chemicals have been added to the water to improve the performance of the mist and deal with new types of fires. This review presents an exhaustive state of the art on additives for water mist technology over the last fifty years. Eleven publishers were reviewed to form the corpus of almost one hundred articles. A systematic review of the articles highlighted that alkali metal compounds have been the main focus of research. Metal-based compounds have also proved to be effective. Surfactants remain an additive of choice in the formulation of fire-fighting foams and as additives for water mist but hydrocarbon surfactants should be preferred to fluor-based ones for environmental reasons. Solvents have proved to be a new, clean and potent class of water mist additives worthy of further investigation. Overall, the toxicology and environmental impacts of most additives have not been addressed or are often overlooked as an important criterion for a water mist additive. [ABSTRACT FROM AUTHOR]

Aggregation behaviour of two cationic surfactants octyltrimethylammonium bromide [OTMAB], decyltrimethylammonium bromide [DTMAB] and two surface active ionic liquids 1-methyl-3-octylimidazolium chloride [C8mim][Cl], 1-methyl-3-decylimidazolium chloride [C10mim][Cl] with anionic dye eosin yellow were investigated by conductometry, UV–Visible spectroscopy and fluorescence spectroscopy. Decrease in CMC of SAILs/surfactants is observed in presence of eosin yellow. Spectroscopic analysis demonstrates a shift in spectra of dye which implies SAILs/surfactants interaction with dye. Binding constant (Ka) obtained by UV–Visible spectroscopy and fluorescence spectroscopy follows the sequence [C10mim][Cl] > [C8mim][Cl] and [DTMAB] > [OTMAB]. The binding constant seems to be mostly dependent on the carbon chain length of these SAILs as well as surfactants. [ABSTRACT FROM AUTHOR]

Saponins are a diverse group of compounds (triterpenoid and steroid glycosides), widely distributed, and characterized by their structures, which differ in the number of sugar units linked in various positions. Saponins have emerged as commercially significant compounds with expanding applications in food, cosmetics, and other pharmaceutical applications as a result of consumer demand for their surfactant properties and have received significant attention due to their biological activities (such as anticancer, antimicrobial, antiprotozoal, delivery adjuvant, anticholesterol, and anti-inflammatory properties). To overcome the processing difficulties given by their complexity, new methods for their extraction and purification strategies must be developed in order to realize their full commercial potential. More attention must be paid to this group of metabolites because many of the active mechanisms are still unknown, and plant-derived saponins have great potential for replacing toxic synthetic or animal-derived surfactants in a wide range of modern commercial products. This review provides an update on the sources, structures, and pharmaceutical applications of phytosaponins and discusses the prospects and challenges of future saponin-based formulations or products. [ABSTRACT FROM AUTHOR]

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The appearance of an extrudate formulation was monitored during hot-melt extrusion (HME) continuous manufacturing over 3 days. The formulation matrix consisted of a polymeric component, copovidone, and a low molecular weight surfactant, polysorbate 80. Based on studies prior to the continuous manufacturing, the desired appearance of the target extrudate is translucent. Although process parameters such as feed rate and screw speed were fixed during the continuous manufacturing, the extrudate appearance changed over time from turbid to translucent. For root-cause investigation, the extrudates were analyzed offline by differential scanning calorimetry (DSC) and advanced polymer chromatography (APC™). Although the polysorbate 80 content of both turbid and translucent extrudates was within target, the glass transition temperature of the turbid extrudate was 2 °C above expected value. The observed turbidity was traced to lot-to-lot variability of the polysorbate 80 used in the continuous manufacturing, where APC™ analysis revealed that the relative content of the low molecular weight component varied from 23% to 27% in correlation with the evolution from turbid to translucent extrudates. This work stresses the importance of taking feeding material variability into account during continuous manufacturing. [ABSTRACT FROM AUTHOR]

A method is proposed for calculating low interfacial tension (IFT) based on molecular dynamics simulation of systems with superdense packing of surfactant molecules at the water–liquid hydrocarbon interface. The interfacial tension was calculated by the molecular dynamics method using the all-atom and coarse-grained models in water–alkane (decane, dodecane) two-phase systems in the presence of various individual surfactants. The following ionic and nonionic surfactants were considered: sodium dodecyl sulfate (SDS), cetyltrimethylammonium chloride (CTAC), sodium dodecylbenzenesulfonate (SDBS), sodium decet-6 sulfate C10E6SO4Na, hexaethylene glycol monodecyl ether (C10E6), triethylene glycol monononadecyl ether (C19E3), and octapropoxypentaethylene glycol monododecyl ether (C12P8E5). It was shown that the interfacial tension decreases to zero when surfactant adsorption increases to the limiting values. [ABSTRACT FROM AUTHOR]

In this review amino acid-surfactant interactions mainly in aqueous solution has been explained. Amino acids and surfactants interactions are important in many studies because of their enhanced effectiveness in both living and non-living worlds. As physicochemical properties are additive, the study of interactions between amino acids and surfactants offer insights into how proteins unfold and denaturate in various media, which further alters with a change in physiological parameters like pH, additives, no of carbon in the chain and temperature. Keeping this in mind, in this review main emphasis has been on conductometric, volumetric and computational studies for detailed exploration of solute–solvent interactions of amino acids and surfactants in aqueous medium and effect of temperature on these interactions. Conductance data has been used to find the critical micelle concentration (CMC) of the surfactant. Using CMC, standard Gibbs free energy of micellization, ( Δ G m 0 ), enthalpy of micellization, ( Δ H m 0 ), entropy of micellization, ( Δ S m 0 ) have been determined for surfactant in presence of amino acids. In volumetric investigation, density data has been utilized to find apparent molar volumes of amino acids, (ϕv) and partial molar volume (ϕ0v), which is used to find soute-solvent interaction. In computational studies the effects of carbon tail length on CMC and aggregation number, (Ag) for the pure Gemini surfactant system were examined and these data were compared with experimental results to find the agreement between different methods. [ABSTRACT FROM AUTHOR]

By combining the unique characteristics of molecular bottlebrushes (MBBs) and the properties of stimuli-responsive polymers, we show that MBBs with randomly grafted poly(n-butyl acrylate) and pH-responsive poly(2-(N,N-diethylamino)ethyl methacrylate) (PDEAEMA) side chains are efficient and robust pH-responsive emulsifiers. Water-in-toluene emulsions were formed at pH 4.0 and disrupted by increasing the pH to 10.0. The emulsion generation and disruption was reversible over the ten cycles investigated, and the bottlebrushes remained intact. The exceptional emulsion stability stemmed from the high interfacial binding energy of MBBs, imparted by their large molecular size and Janus architecture at the interface, as evidenced by the interfacial jamming and wrinkling of the assemblies upon reducing the interfacial area. At pH 10.0, PDEAEMA became water-insoluble, and the MBBs desorbed from the interface, causing de-emulsification. Consequently, we have shown that the judicious design of MBBs can generate properties of particle emulsifiers from their large size, while the responsiveness of the MBBs enables more potential applications.

Abstract There is a substantial body of literature exploring the challenges associated with exploring and exploiting these underground resources. Unconventional resources, particularly heavy oil reservoirs, are critical for meeting ever-increasing global energy demand. By injecting surfactants into heavy oil, chemically enhanced oil recovery (EOR) may enable emulsification, which may reduce the viscosity of heavy oil and facilitate extraction and transportation. In this work, a large experimental dataset, containing 2020 data points, was extracted from the literature for modeling oil-in-water (O/W) emulsion viscosity using machine learning (ML) methods. The algorithms used pressure, temperature, salinity, surfactant concentration, type of surfactant, shear rate, and crude oil density as inputs. For this purpose, five ML algorithms were selected and optimized, including adaptive boosting (AB), convolutional neural network (CNN), ensemble learning (EL), artificial neural network (ANN), and decision tree (DT). A combined simulated annealing (CSA) method was utilized to optimize all algorithms. With AARE, R2, MAE, MSE, and RMSE values of 8.982, 0.996, 0.004, 0.0002, and 0.0132, respectively, the ANN predictor exhibited higher accuracy in predicting O/W emulsion viscosity for total data (train and test subsets combined). A Monte-Carlo sensitivity analysis was also performed to determine the impact of input features on the model output. By using the proposed ML predictor, expensive and time-consuming experiments can be eliminated and emulsion viscosity predictions can be expedited without the need for costly experiment.

This article examines the effect of CTAB on the interfacial rigidity of silica nanoparticle films at the oil/water interface. The authors demonstrate that increasing CTAB concentrations reduce the rigidity of the nanoparticle layer, which in turn influences the structural integrity of bicontinuous interfacially jammed emulsion gels (bijels). [Display omitted] • CTAB charge screening lowers interfacial rigidity of nanoparticle assemblies. • Modulation of charge screening via ionic strength. • Charge screening also promotes CTAB adsorption on silica nanoparticles. • Interfacial rigidity control enhances bijel uniformity and structure. Functionalizing colloidal particles with oppositely charged surfactants is crucial for stabilizing emulsions, foams, all-liquid structures, and bijels. However, surfactants can reduce the attachment energy, the driving force for colloidal self-assembly at interfaces. An open question remains on how the inherent interfacial activity of cationic surfactants influences the interfacial rigidity of particle-laden interfaces. We hypothesize that charge screening among cationic surfactants regulates the rigidity of oil/water interfaces by reducing the attachment energy of nanoparticles. We investigate the interfacial rigidity of cetyltrimethylammonium bromide (CTAB) functionalized silica nanoparticles (Ludox® TMA) by analyzing the shape deformation of 1,4-butanediol diacrylate (BDA) droplets under varying salt and alcohol concentrations. The nanoparticle packing density is assessed using scanning electron microscopy. Attachment energy is characterized through interfacial tension measurements, three-phase contact angle analysis, and CTAB adsorption studies. We also examine the effects of interfacial rigidities on the structure of bijel films formed via roll-to-roll solvent transfer-induced phase separation (R2R-STrIPS) using confocal laser scanning microscopy. Increasing salt and alcohol concentrations decrease the interfacial rigidity of CTAB-functionalized nanoparticle films by reducing the interfacial tension. The contact angle has a minor influence on the rigidity. These results indicate that CTAB charge screening weakens the nanoparticle attachment energy to the interface. Controlling the rigidity enables the mass production of bijel sheets with consistent flatness, which is crucial for their potential applications in catalysis, energy storage, tissue engineering, and filtration membranes. [ABSTRACT FROM AUTHOR]

[Display omitted] Hypothesis: Limited research has been conducted on the influence of chelating agents on the self-assembly process in surfactant solutions. The traditional approach assumes the chelating agent only interferes as a salting-out ion, therefore promoting surfactant separation. However, the opposite behavior has been observed for iminodipropionate based surfactants, in which the presence of chelating agents of the aminopolycarboxylate type increases solubility of nonionic ethoxylated surfactants in mixed micellar systems. Specific interaction between chelating agents-surfactants can be an important parameter in the self-assembly processes. Experiments: Physicochemical properties of solutions containing amphoteric surfactant and tetrasodium glutamatediacetate have been investigated. Macroscopic properties, such as viscosity and cloud point, were evaluated in the presence of a non-water-soluble alkyl ethoxylated surfactant. Interactions between amphoteric surfactant and chelating agent were monitored by NMR spectroscopy, including 13C chemical shift and lineshape analysis as well as 1H diffusometry. Findings: The study reveals that there is an interaction between the head group of the surfactant and the chelating agent forming oligomeric surfactant analogues with larger hydrophilic moieties, which results in smaller, more spherical micelles. The combined interactions provide possibilities for tuning the aggregation behavior of systems containing surfactants and chelating agents, and with that, the macroscopic properties of the system. [ABSTRACT FROM AUTHOR]

The gradients in surfactant distribution at a fluid-fluid interface can induce fluid flow known as the Marangoni flow. Fluid interfaces found in biological and environmental systems are seldom clean, where mixtures of various surfactants are present. The presence of multi-component surfactant mixtures introduces the possibility of interactions among constituents, which may impact Marangoni flows and alter flow dynamics. We employed flow visualization, surface tension and reaction kinetic measurements, and numerical simulations to quantitatively investigate the Marangoni flows induced by the reacting surfactant mixtures. Different binary surfactant mixtures were utilized for comparative analysis. The impact of surfactant interactions on Marangoni flows is confirmed through the observation of diverse complex flow patterns that result from the combination of oppositely charged surfactants in varying composition ratios and concentrations. Unique flow patterns originate from the composition-dependent interfacial phenomena upon mixing surfactants. Our findings provide vital insights that could be used to guide the development of effective oil remediation or the spreading of waterborne pathogens in contaminated regions. [ABSTRACT FROM AUTHOR]

The catalyst's particle size plays a crucial role in enhancing photocatalytic performance. However, it is still unclear to analyse the mechanism by which surfactants affect the particle size of photocatalysts from the perspective of crystal growth. Herein, ZnS nanomaterials with different particle sizes were synthesized using a simple solid-state chemical synthesis method, and the intrinsic influence mechanism between surfactant and catalyst particle size was analyzed from the perspective of crystal growth. It was discovered that the particle size of ZnS kept getting smaller due to changes in polyethylene glycol, cetyltrimethylammonium bromide, and sodium dodecyl sulfate. Analyzing the reasons revealed that the catalyst's particle size was related to the type of surfactant: anionic surfactants could reduce the catalyst size. Correspondingly, the catalyst with a smaller particle size has the optimal performance for photocatalytic hydrogen production. Photocatalysts Z-SDS exhibited outstanding photocatalytic performance, yielding 11.47 mmol/g of hydrogen after a 5 h illumination. Furthermore, the intrinsic influence mechanism between anionic and cationic surfactants, photocatalyst particle size, and catalytic performance was investigated. This investigation provides a new idea for synthesizing small-size and high-performance photocatalysts. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: Chiral covalent organic frameworks (COFs) have shown promising applications in asymmetric catalysis, enantiomer separation and chiral recognition due to their tunable structures and permanent porosity. Currently, synthesis of chiral COFs mainly relies on direct‐ synthesis method which requires asymmetric monomers to polymerize and crystallize with symmetric monomers and post‐synthesis method which has been greatly limited to having complete reactions with the micro‐/meso‐sized pores of COFs. Recently, the synthesis of two‐dimensional COFs by covalent replacement of chiral competitor has been reported. Herein, we present the synthesis of three types of 3D COFs with tunable chirality using chiral amino acid derivative surfactant as inducer in water under ambient conditions. The hydrogen bonds and electrostatic interactions between amino acid derivative surfactant and monomers as well as their precursors facilitate the transfer of the chirality. [ABSTRACT FROM AUTHOR]

Photothermal conversion of light into heat energy is an intrinsic optical property of metal nanoparticles when irradiated using near-infrared radiation. However, the impact of size and shape on the photothermal behaviour of gold nanomakura particles possessing optical absorption within 600–700 nm as well as on incorporation in hydrogels is not well reported. In this study, nanomakura-shaped anisotropic gold nanoparticles (AuNMs) were synthesized via a surfactant-assisted seed-mediated protocol. Quaternary cationic surfactants having variable carbon tail length (n = 16, 14, 12) were used as capping for tuning the plasmon peak of gold nanomakura within a 600–700 nm wavelength. The aspect ratio as well as anisotropy of synthesized gold nanomakura can influence photothermal response upon near-infrared irradiation. The role of carbon tail length was evident via absorption peaks obtained from longitudinal surface plasmon resonance analysis at 670, 650, and 630 nm in CTAB-AuNM, MTAB-AuNM, and DTAB-AuNM, respectively. Furthermore, the impact of morphology and surrounding milieu of the synthesized nanomakuras on photothermal conversion is investigated owing to their retention of plasmonic stability. Interestingly, we found that photothermal conversion was exclusively assigned to morphological features (i.e., nanoparticles of higher aspect ratio showed higher temperature change and vice versa irrespective of the surfactant used). To enable biofunctionality and stability, we used kappa-carrageenan- (k-CG) based hydrogels for incorporating the nanomakuras and further assessed their photothermal response. Nanomakura particles in association with k-CG were also able to show photothermal conversion, depicting their ability to interact with light without hindrance. The CTAB-AuNM, MTAB-AuNM, and DTAB-AuNM after incorporation into hydrogel beads attained up to ≈17.2, ≈17.2, and ≈15.7 °C, respectively. On the other hand, gold nanorods after incorporation into k-CG did not yield much photothermal response as compared to that of AuNMs. The results showed a promising platform to utilize nanomakura particles along with kappa-carrageenan hydrogels for enabling usage on nanophotonic, photothermal, and bio-imaging applications.

Abstract Investigating surfactant effects on the floatability of Wiser bituminous coal holds significant importance in improving coal cleanliness and utilization value. Using density functional theory and molecular dynamics simulation methods, this study constructed models of Wiser bituminous coal and examined the impact of different surfactants, including the anionic surfactant sodium dodecyl benzene sulfonate, the cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB), and the non-ionic surfactant fatty alcohol ethoxylated ether. The focus was on investigating the charge distribution characteristics of these molecules and the modifying effect of binary surfactants on the hydrophobicity of bituminous coal. Results revealed that the maximum electrostatic potential was concentrated near oxygen/nitrogen/sulfur-containing functional groups like sulfonic acid groups, quaternary ammonium cations, ethylene oxide, hydroxyl groups, carboxyl groups, and sulfur bonds. These functional groups exhibited a propensity for accepting/delivering electrons to form hydrogen bonds. Among the surfactants tested, CTAB revealed the slightest difference in frontier orbital energy, measuring 3.187 eV, thereby demonstrating a superior trapping ability compared with the other two surfactants. Adsorption reactions within the system were determined to be spontaneous, with over 60% of the interaction force attributed to electrostatic forces. Moreover, the repulsive force magnitude with water molecules followed the trend: sulfonate group (2.20 Å)