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The synthesis of mesoporous material by utilizing palm oil boiler ash (POBA) waste as the silica source and methyl ester sulfonate (MES) surfactant as the template for a high-porosity was investigated for free fatty acids (FFA) adsorption. The research was initiated with silica extraction from POBA by sodium hydroxide addition through the sol-gel precipitation method. Silica modification was carried out with MES surfactant and 3-aminopropyltrimethoxysilane (APTMS) as the co-structure-directing agent (CSDA) in different calcination temperatures. Mesoporous silica-POBA (MS-POBA) free template had a surface area, pore diameter, and pore volume (41.033 m2/g, 4.180 nm, and 0.250 cm3/g) lower than MS-POBA with the template (71.0147 m2/g, 7.923 nm, and 0.524 cm3/g). The ability of MS-POBA to adsorb FFA reached its optimum conditions with an adsorption time of 20 min and an adsorbent dosage of 0.24 g. The FFA removal by MS-POBA with the template was found to have higher adsorption ability, which was 35.54%, compared to the MS-POBA free template of 26.68%. The high porosity of MS-POBA with a template makes the FFA adsorption capacity of this material higher than MS-POBA free template.

In this study, we explored traditional methods commonly found in the literature to analyze how surfactants and polymers interact during the synthesis of polyesters in emulsion systems. The study justifies its focus on micellar catalysis by exploring its effectiveness and suggesting methods for enhancing the synergy among surfactants, reactants, and catalys. We looked at factors like surface tension, critical micelle concentration, micelle shapes, aggregation numbers, and interfacial phenomena in the process of macromolecular packing in emulsion polycondensation. A surfactant-water system consisting of dodecylbenzenesulfonic acid and sodium dodecyl sulfate was employed. Polyesters were prepared from glycerol, ethylene glycol, diethylene glycol, and dicarboxylic acids in a surfactant-water system under mild conditions ranging from 70-150 °C. FTIR and 1H NMR confirmed the esterification. Differential scanning calorimetry indicated no crystallinity and a glass transition temperature range of –53 to –46 °C, typical of soft matter. The resulting polymers had molecular weights ranging from 1180 – 6800 g/mol. We found that these polymer aggregate shapes are able to respond by changing their sizes, both in bulk and at the air-solution interface, when the concentration of surfactant is increased above the critical micelle concentration. The results showed narrow spherical and ellipsoidal polymer aggregates, and the system was found to be suitable for green chemistry applications.

The use of the cholinesterase enzyme as a component of the analytical system has made it possible to develop a new kinetic-spectrophotometric method, which is alternative to the pharmacopoeial method, for determining the quaternary ammonium salt – ethonium in the substance and a dosage form. This method is characterized by high sensitivity and specificity, and is relatively cheap. The relative standard deviation of the procedure does not exceed 2.7 %, and the limit of quantification is 17 ng/mL.

The residual oil left behind after water flooding in petroleum reservoirs can be mobilized by surfactant formulations that yield ultralow interfacial tension (IFT) with oil. However, finding ultralow IFT surfactant formulations is difficult for high-temperature, off-shore, carbonate reservoirs. These reservoirs are often water-flooded with seawater (with a lot of divalent ions), which is often incompatible with many surfactants at high temperatures. The goal of this research is to develop a surfactant formulation for an off-shore carbonate reservoir at 100°C previously flooded by seawater. Surfactant–oil–brine phase behavior was studied for formulations, starting from a single surfactant to mixtures of surfactants and a co-solvent. Mixtures of three surfactants and one co-solvent were needed to produce ultralow IFT formulations for the oil of interest. The surfactant system with polymer mobility control was tested in crushed reservoir rock packs. The cumulative oil recovery was >99% for the surfactant–polymer (SP) flood with an optimal salinity gradient. The constant salinity SP floods with seawater increased oil recovery significantly beyond the water flood (cumulative oil recovery >91%), even though the recovery was lower than that of the optimal salinity gradient SP flood. Our experimental work demonstrates the effectiveness of the surfactant formulation for a high-temperature carbonate reservoir at seawater salinity.

The dyeing process with natural dyes has disadvantages, including poor color fastness. A mordanting process is required to overcome these disadvantages. Conventional mordanting processes often use metal salts. This research will substitute the mordanting process using surfactants as mordant substances. The pH of the process influences the application of dyeing with natural dyes. This study aims to determine the effect of the pre-mordant process using surfactants and the pH of the dyeing process on the color characteristics of cotton and silk fabrics dyed with Cocos nucifera L dye extract. The surfactants used were cationic and non-ionic polymeric surfactants. This study was conducted in phases. The first phase involved the extraction of coconut fiber, and the second phase involved pre-mordanting the fiber with surfactants. The third stage is the dyeing process, which has variations in pH 3, 7, and 9. The evaluation results show that cationic surfactants have the potential to be used as a mordant and provide an increased anti-bacterial effect on processed fabrics. The optimal use of cationic surfactants was obtained using a concentration of 9 g/L and pH 7 for the cotton dyeing process. The optimum concentration was obtained at 9 g/L for the silk dyeing process, and the dyeing pH was 3.

Acute lung Injury leads to alterations in surfactant lipid composition and metabolism. Although several mechanisms contribute to dysregulated surfactant metabolism, studies investigating in vivo surfactant metabolism are limited. The aim of this study is to characterise surfactant phospholipid composition and flux utilising a stable isotope labelling technique in mechanically ventilated paediatric patients. Paediatric patients (methyl-D9-choline chloride followed by the endotracheal instillation of 100 mg/kg of exogenous surfactant after 24 h. Bronchioalveolar fluid samples were taken at baseline and 12, 24, 36, 48, 72 and 96 h after methyl-D9-choline infusion. Nine participants (median age of 48 days) were recruited. The primary phosphatidylcholine (PC) composition consisted of PC16:0/16:0 or DPPC (32.0 ± 4.5%). Surfactant supplementation resulted in a 30% increase in DPPC. Methyl-D9 PC enrichment was detected after 12 h and differed significantly between patients, suggesting variability in surfactant synthesis/secretion by the CDP-choline pathway. Peak enrichment was achieved (0.94 ± 0.15% of total PC) at 24 h after methyl-D9-choline infusion. There was a trend towards reduced enrichment with the duration of mechanical ventilation prior to study recruitment; however, this was not statistically significant (p = 0.19). In this study, we demonstrated the fractional molecular composition and turnover of surfactant phospholipids, which was highly variable between patients.

Abstract Using household detergents to clean oil stains has always caused global concerns, as these detergents negatively impact the ecosystem and are toxic. Therefore, it is essential to effectively attenuate the adhesion force between oil stains and substrates to create an easy and detergent‐saving cleaning pathway. To address this challenge, we herein develop a strategy to reduce the strength of oil adhesion on common substrates by ∼20 times through a lamination layer, which contains phase‐transitioned lysozyme nanofilm (PTL) and cellulose nanocrystals (CNCs). The resultant CNC/PTL coating significantly enhances the capability of cleaning oil stains in an underwater detergent‐free manner; this strategy is applicable to edible oil packaging material and tableware, without impairing the usability and aesthetics of these materials. This coating exhibits excellent mechanical stability and regeneration characteristics through simple soaking, ensuring its robustness in real applications in an infinite life cycle. By eliminating 100% detergent in routine cleaning, the CNC/PTL coating demonstrated remarkable cost‐effectiveness, saving 57.7% of water and 83.3% of energy when washing tableware only with water. This work presents an ingenious design to create oil‐repellent packaging materials and tableware toward detergent‐free water‐cleaning pathways, thereby greatly reducing the negative environmental impact of surfactant emissions.

The continuous deepening of coal-seam extraction has sharply increased both gas pressure and content. The use of viscoelastic surfactant fracturing fluids (VESFFs) has been demonstrated to effectively improve coal-seam permeability and mitigate the occurrence of gas disasters. After injection into coal, VESFFs interact with the coal and affect its surface characteristics. In this study, to characterize changes in zeta potential, oxygen-containing functional groups, and the microcrystalline structure of hard and soft coal surfaces under the influence of VESFFs with different formulations, zeta potential measurements and Fourier-transform infrared and Raman spectroscopies were performed. The VESFFs enhanced the electrostatic repulsion between the pore wall and coal particles, which is favorable for the removal of coal particles from hard and soft coal surfaces. The combination of cationic with zwitterionic viscoelastic surfactants (VESs) in the VESFFs exposed more hydrophilic functional groups on the surfaces of hard and soft coal, increasing wettability and affecting nanometer pores. A VESFF based on anionic and zwitterionic VESs as the primary agents could enhance the extension of the aromatic layer (La) of the aromatic crystal nuclei and reduce the interlayer spacing (d002) of hard and soft coal, thereby increasing the volume of micropores. This research offers theoretical guidance for optimizing the primary components of VESFFs and elucidates the mechanism through which VESFFs act on nanopores in coal from a microscopic perspective.

Due to their high surface area and low weight, silica aerogels are ideally suited for several uses, including drug delivery, catalysis, and insulation. Oil–water–oil (OWO) double emulsion is a simple and regulated technique for encasing a volatile oil phase in a silica shell to produce hollow silica (SiO2) aerogel particles by using hydrophilic and hydrophobic emulsifiers. In this study, the oil–water–oil (OWO) double emulsion method was implemented to synthesize surface-modified hollow silica (SiO2) aerogel particles in a facile and effective way. This investigation mainly focused on the influence of the N-hexane-to-water glass (OW) ratio (r) in the first emulsion, silica (water glass) content concentration (x), and surfactant concentration (s) variations. Furthermore, surface modification techniques were utilized to customize the aerogel’s characteristics. The X-ray diffraction (XRD) patterns showed no imprints of impurities except SiO2. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images highlight the hollow microstructure of silica particles. Zeta potential was used to determine particle size analysis of hollow silica aerogel particles. The oil–water–oil (OWO) double emulsion approach was successfully employed to synthesize surface-modified hollow silica (SiO2) aerogel particles, providing precise control over the particle characteristics. By the influence of the optimization condition, this approach improves the aerogel’s potential applications in drug delivery, catalysis, and insulation by enabling surface modifications.

Self-assembly of surfactants into complex structures is key to the performance of many formulated products, which form a significant fraction of the world’s manufactured goods. Here we adopt the dissipative particle dynamics simulation approach to explore the self-assembly process of surfactants, with the aim of understanding what information can be obtained that may correlate with an increased zero-shear viscosity of surfactant based products. To this end we experimentally measured the zero-shear viscosity of mixed micelle systems comprised of cocoamidopropyl betaine (CAPB) and sodium lauryl sarcosinate (SLSar), as a function of the CAPB/SLSar mass ratio and pH, and characterised the early stages of self-assembly of the same systems computationally. From simulation we identify three distinct behaviors in the micellar self-assembly process (logarithmic, linear and cubic growth) which we find show some degree of correlation with the experimental zero-shear viscosity. Owing to the relatively short simulation times required, this may provide formulation scientists with a practical route to identify regions of interest (i. e. those with a desired zero-shear viscosity) prior to synthesising de novo (potentially natural) surfactants.

The performance of Candida antarctica lipase B (CALB) has been evaluated in 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4)/water mixtures in a wide range of molar fractions (χBMIMBF4) with and without 1-dodecyl-3-methylimidazolium tetrafluoroborate (C12-MIMBF4), a surfactant derived from BMIMBF4. The main aim of this work is to evaluate the influence of χBMIMBF4 over micellar aggregates to assess the activity of enzymatic reactions. The investigated reaction corresponds to the hydrolysis of the substrate p-nitrophenyl laureate in each χBMIMBF4. The kinetic study for χBMIMBF4 at around 0.2 proved to be a border point in enzymatic activity. At χBMIMBF4 = 0.1, the lipase activity increases in the presence of C12-MIMBF4. However, at higher concentrations, BMIMBF4 has a negligible effect over the lipase activity. These results suggest specific interactions between water and BMIMBF4 molecules in relation to CALB. This research highlights the superactivity phenomenon driven by the reaction media and the micelle interface. In this interfacial interaction, BMIMBF4 acts directly on the changes induced on the enzyme upon its interaction with the micellar interface. This study opens a green perspective toward the biocatalysis field.

By utilizing the reaction of lauryl chloride, potassium thiocynate, and 2,4-dinitroaniline, the novel non-ionic surfactant 1-(2, 4-dinitrophenyl)-3-dodecanoylthiourea (DDT) was produced in high yield. Various spectroscopic techniques (1HNMR, 13CNMR, and UV-V) have been used to elucidate the chemical structure of DDT. Additionally, its electrochemical behaviour (electrochemical fate) was elucidated using a cyclic, square wave, and differential pulse voltammetry through a wide pH range. The limit of detection (LOD) and limit of quantification (LOQ) values of the compound were also determined using Square wave voltammetry (SWV). A fascinating fact observed is that the electroactive moieties in the compound are getting oxidized and reduced at a potential very close to 0.0 V, and the potential of the human body is 0.07 V, so the compound investigated can serve as an efficient candidate for the drug deliveries and metabolism processes.

Photo-galvanic cells are based on the diffusion of ions in the electrolyte (a mixture of sensitizer, reductant, alkali, surfactant, and solvent). The photogalvanics is characterized by the abrupt jump in the photo-potential during charging of the cell. Photo-galvanic cells have been widely studied using the complete electrolyte. The migration of current by ions gives impression that any of the ionic species individually (like sensitizer/reductant/etc.) may show current, potential, and photogalvanics. This aspect of photogalvanics of individual chemical components is missing in the literature. Therefore, the photogalvanics of the individual chemicals, mixtures of the chemicals, and complete electrolyte have been studied in present research to have insight into (i) the genesis of the current and potential generated from the cell in non-illuminated state (dark conditions), and (ii) the necessary chemical conditions required for the photogalvanics.The average open-circuit potential (Voc) and short-circuit current (Isc) in dark conditions for water, Lactic acid reductant, Cocamidopropyl betaine surfactant, Carmoisine-A dye, NaOH alkali, complete electrolyte (at low pH), and complete electrolyte (at very high pH) is 286 mV, 4 µA; 214 mV, 3 µA; 278 mV, 4 µA; 268 mV, 9 µA; 295 mV, 8 µA; 278 mV, 8 µA; and 463 mV, 253 µA, respectively. The average Voc and Isc from illuminated water, Lactic acid reductant, Cocamidopropyl betaine surfactant, Carmoisine-A dye, NaOH alkali, complete electrolyte (at low pH), and complete electrolyte (at very high pH) is 296 mV, 3 µA; 182 mV, 4 µA; 218 mV, 4 µA; 135 mV, 3 µA; 275 mV, 9 µA; 167 mV, 6 µA; and 731 mV, 2500 µA, respectively. Thus, no photogalvanics has been observed for individual chemical components, and mixtures of two or more chemical components of the electrolyte. The photogalvanics is observed only for complete electrolyte at high pH.

Lyotropic liquid crystals (LLCs) produced by the self-assembly of surfactant in water represent an important class of highly ordered soft materials that have a wide range of applications. This study investigates the LLCs formed by a zwitterionic surfactant (tetradecyldimethylaminoxide, C14DMAO) in water. The organization of C14DMAO within the LLCs was determined based on a detailed analysis of small-angle X-ray scattering measurements and polarized microscopy observations of a typical sample. Additional to the singe-phase region, which has a hexagonal organization, several two-phase regions were observed, exhibiting the coexistence of hexagonal/cubic, cubic/lamellar, and hexagonal/lamellar phases. The phase behavior showed an obvious dependence on temperature, with more pronounced two-phase regions at lower temperatures. Using the LLCs as a matrix, Au nanospheres, nanoellipsoids, and nanorods were prepared without requiring additional reducing reagents. These three- and one-dimensional Au nanomaterials could be converted to two-dimensional plates via the introduction of a small amount of cationic surfactant to the LLCs, such as cetyltrimethylammonium bromide (CTAB) and 1-hexadecyl-3-methylimidazolium bromide ([C16MIm]B), which showed pronounced surface-enhanced Raman scattering activity towards solid rhodamine. The LLCs loaded with CTAB (or [C16MIm]B) and HAuCl4 exhibited slightly different structures and mechanical strength from the original LLCs, thereby forming a new class of highly crowded colloidal materials.

This paper investigates the effects of sodium laureth sulfate (SLES) on the wettability of the surface of the two most common recycled plastics in refrigeration equipment: HIPS (high-impact polystyrene) and ABS (acrylonitrile–butadiene–styrene). These plastics, in the form of flakes, were identified on the basis of their FTIR spectra, and then, they were subjected to a study of contact angles using the sessile droplet method. The solutions for the angle analysis included tap water with the addition of SLES. The results of this study showed that at SLES concentrations of 0.1 g/L and 0.2 g/L, the differences in the contact angles for HIPS and ABS were 10.76° and 10.10°, respectively. This research confirmed the potential of using SLES as a support for the flotation separation of plastics with similar densities and surface characteristics, such as HIPS and ABS.

Recently the urea and urinated wastewater electrolysis process has shown promising technology for hydrogen fuel green production in addition to denitrification of wastewater. However, to make the process economically valuable, the electrocatalysts nanoarchitecture, nanometer size, shape, facets, and composition need to be engineered to boost the urea oxidation reaction (UOR). This work demonstrates a simple and novel approach to the synthesis of mesoporous nickel phosphate nanoparticles (meso-NiPO) via chemical deposition from a surfactant liquid crystal template. Typically, the nickel ions dissolved in the aqueous domain of the hexagonal liquid crystalline phase of the Brij®78 template were chemically reacted with the sodium phosphate solution to precipitate the mesoporous nickel phosphate nanoarchitecture after washing up the surfactant. The physicochemical characterizations show the meso-NiPO exhibits an amorphous highly mesoporous structure with a higher specific surface area (43.50 m2/g) compared to the bare nickel phosphate (bare-NiPO, 4.26 m2/g) prepared in the absence of surfactant. The electrochemical performance of meso-NiPO electrocatalyst for the urea oxidation reaction in alkaline solution exhibits superior activity including a lower oxidation onset potential (0.30 V vs. Ag/AgCl), charge transfer resistance (3.35 O) and mass activity of 700.7 mA/cm2 mg at the oxidation potential of 0.6 V vs. Ag/AgCl. Moreover, the meso-NiPO reveals long-term stability, and 97.5% of the steady-state oxidation current was maintained after the 3-hour urea electrolysis test. Using an H-shape urea electrolyzer, the corresponding cathodic hydrogen production rate reached 415 µmol/h and a Faradic efficiency of 96.8 % at an applied bias of 2.0 V. The electroactivity high performance of the mesoporous nickel phosphate is ascribed to the high specific surface area and mesoporous architecture that provide efficient charge transfer, as well as mass transport of the electroactive species. The chemical deposition from a surfactant liquid crystal template has the advantages of a one-pot template, applicable to the synthesis of a wide range of nanomaterials with various compositions and nanoarchitectures at room temperature for application in electrochemical energy production and storage systems.

Abstract The influence of molecular fragmentation and parameter settings on a mesoscopic dissipative particle dynamics (DPD) simulation of lamellar bilayer formation for a C10E4/water mixture is studied. A “bottom-up” decomposition of C10E4 into the smallest fragment molecules (particles) that satisfy chemical intuition leads to convincing simulation results which agree with experimental findings for bilayer formation and thickness. For integration of the equations of motion Shardlow’s S1 scheme proves to be a favorable choice with best overall performance. Increasing the integration time steps above the common setting of 0.04 DPD units leads to increasingly unphysical temperature drifts, but also to increasingly rapid formation of bilayer superstructures without significantly distorted particle distributions up to an integration time step of 0.12. A scaling of the mutual particle–particle repulsions that guide the dynamics has negligible influence within a considerable range of values but exhibits apparent lower thresholds beyond which a simulation fails. Repulsion parameter scaling and molecular particle decomposition show a mutual dependence. For mapping of concentrations to molecule numbers in the simulation box particle volume scaling should be taken into account. A repulsion parameter morphing investigation suggests to not overstretch repulsion parameter accuracy considerations.

A three-phase foam is considered one of the promising advanced materials for fighting fires. However, the preparation conditions, cost and effect are key factors for industrial applications. In this study, new three-phase foam systems with fly ash and a complex surfactant are proposed. Five types of surfactants alcohol polyoxyethylene ether sodium sulfate, coconut oil diethanolamine, sodium lauryl sulfate, polyacrylamide and polyether-modified silicone resin emulsion were selected as foaming agents. Through laboratory experiments, the effect on the expansion ratio and foam stability of the surfactant type/concentration, fly ash particle concentration/size and pH were investigated. The foaming condition was determined by numerical optimization. The results of this study may serve as a reference for understanding the preparation of a novel threephase foam. It is hoped that this work could provide useful guidance for the preparation of efficient three-phase fire-extinguishing foam for the safe guarding of process safety in the field of chemical production, transportation, and storage suitable for drug delivery than Al12P12 and Al12N12 based on their recovery times.

The current trend in microbiological research aimed at limiting the development of biofilms of multidrug-resistant microorganisms is increasingly towards the search for possible synergistic effects between various compounds. This work presents a combination of a naturally occurring compound, β-aescin, newly synthesized alkylamidobetaines (AABs) with a general structure—CnTMDAB, and antifungal drugs. The research we conducted consists of several stages. The first stage concerns determining biological activity (antifungal) against selected multidrug-resistant strains of Candida glabrata (C. glabrata) with the highest ability to form biofilms. The second stage of this study determined the activity of β-aescin combinations with antifungal compounds and alkylamidobetaines. In the next stage of this study, the ability to eradicate a biofilm on the polystyrene surface of the combination of β-aescin with alkylamidobetaines was examined. It has been shown that the combination of β-aescin and alkylamidobetaine can firmly remove biofilms and reduce their viability. The last stage of this research was to determine the safety regarding the cytotoxicity of both β-aescin and alkylamidobetaines. Previous studies on the fibroblast cell line have shown that C9 alkylamidobetaine can be safely used as a component of anti-biofilm compounds. This research increases the level of knowledge about the practical possibilities of using anti-biofilm compounds in combined therapies against C. glabrata.

Lipases can catalyze synthesis reactions in a micro aqueous system, producing useful partial glycerides (mono- and diglycerides), and these compounds are commonly utilized in different products as surfactants. Depending on the microbial sources for lipases, immobilization conditions, and starting substrates for synthesis reaction, the composition and yields of the resulting partial glycerides could be variable. These differences could lead to the final efficacy of partial glycerides as surfactants in targeted products. Therefore, it is necessary to establish a group of immobilized lipases from different microbial sources with information about substrate specificity to produce effective partial glycerides for various product types. Here, lipases from thermophilic Geobacillus stearothermophilus and Anoxybacillus flavithermus were prepared with a simple partial purification method, and after immobilization, these lipases were tested to synthesize partial glycerides using different types of decanoic acids. The distinct product patterns were analyzed using HPLC. Both immobilized lipases showed the highest substrate selectivity to decanoic acids in common, producing mainly glyceryl monodecanoate. However, commercial immobilized lipases from Thermomyces lanuginosus produced the largest glyceryl monodecanoate from methyl decanoate. These results indicate the importance of immobilization conditions like different microbial sources and substrates and the need for their optimal combination.

The onset and early stages of dynamic wetting on different hydrophobic surfaces is investigated experimentally for aqueous solutions of two commercial trisiloxane surfacants of similar chemical structure, one of which exhibits superspreading behaviour, in order to investigate the spreading dynamics independently of the surface activity. Superspreading, or the ability of a surfactant solution to spread on a surface beyond the state determined by thermodynamic equilibrium, has been investigated for more than 30 years however its physical mechanism remains poorly understood to date despite its important applications in the formulation of agrochemicals. Surfactant solutions were prepared by dissolving S233 and S240 surfactants (Evonik Industries AG, Essen, Germany) into de-ionised water at a weight concentration of 0.1%. Drops of surfactant solutions and pure water were deposited on three horizontal substrates with different wettability (equilibrium contact angle of water ranging between 55∘ and 100∘), and observed from below with a high-frame rate camera to visualise the advancing contact line. The spreading ratio of drops as a function of time was extracted from high-speed videos by digital image processing. Results reveal that the superspreading solution exhibits an intermittent spreading rate, as well as peculiar features of the contact line, which are not observed for the non-superspreading solution, and confirm the superspreading effect becomes less significant when the surface energy of the substrate is decreased.

Surfactants are widely used in the synthesis of nanoparticles, as they have a remarkable ability to direct their growth to obtain well-defined shapes and sizes. However, their post-synthesis removal is a challenge, and the methods used often result in morphological changes that defeat the purpose of the initial controlled growth. Moreover, after the removal of surfactants, the highly active surfaces of nanomaterials may undergo structural reconstruction by exposure to a different environment. Thus, ex situ characterization after air exposure may not reflect the effect of the cleaning methods. Here, combining X-ray photoelectron spectroscopy, in situ infrared reflection absorption spectroscopy, and environmental transmission electron microscopy measurements with CO probe experiments, we investigated different surfactant-removal methods to produce clean metallic Pt nanoparticles from surfactant-encapsulated ones. It was demonstrated that both ultraviolet-ozone (UV-ozone) treatment and room temperature O2 plasma treatment led to the formation of Pt oxides on the surface after the removal of the surfactant. On the other hand, when H2 was used for plasma treatment, both the Pt0 oxidation state and nanoparticle size distribution were preserved. In addition, H2 plasma treatment can reduce Pt oxides after O2-based treatments, resulting in metallic nanoparticles with clean surfaces. These findings provide a better understanding of the various options for surfactant removal from metal nanoparticles and point toward non-thermal plasmas as the best route if the integrity of the nanoparticle needs to be preserved.

Ropinirole is a non-ergolinic dopamine agonist used to manage Parkinson’s disease and it is characterized by poor oral bioavailability. This study aimed to design and develop advanced drug delivery systems composed of poloxamer 407, a non-ionic surfactant (Tween 80), and cyclodextrins (methyl-β-CD or hydroxy-propyl-β-CD) for possible brain targeting of ropinirole after nasal administration for the treatment of Parkinson’s disease. The hybrid systems were formed by the thin-film hydration method, followed by an extensive physicochemical and morphological characterization. The in vitro cytotoxicity of the systems on HEK293 cell lines was also tested. In vitro release and ex vivo mucosal permeation of ropinirole were assessed using Franz cells at 34 °C and with phosphate buffer solution at pH 5.6 in the donor compartment, simulating the conditions of the nasal cavity. The results indicated that the diffusion-controlled drug release exhibited a progressive increase throughout the experiment, while a proof-of-concept experiment on ex vivo permeation through rabbit nasal mucosa revealed a better performance of the prepared hybrid systems in comparison to ropinirole solution. The encouraging results in drug release and mucosal permeation indicate that these hybrid systems can serve as attractive platforms for effective and targeted nose-to-brain delivery of ropinirole with a possible application in Parkinson’s disease. Further ex vivo and in vivo studies to support the results of the present work are ongoing.

The hybridization of inorganic and organic components is a promising strategy to build functional materials. Among several functions, luminescence is an important function which should be considered for practical usage. Inorganic–organic hybrid luminescent materials have been investigated as phosphors, sensors, and lasers. Organic luminescent centers such as dye molecules have often been hybridized with inorganic matrices. Polyoxometalate anions (POMs) are effective inorganic luminescent centers due to their luminescent properties and structural designability. However, most luminescent POM components are limited to lanthanide-based POMs. In this report, a photoluminescent inorganic–organic hybrid crystal based on a non-lanthanide POM was successfully synthesized as a single crystal. Anderson-type hexamolybdochromate ([CrMo6O18(OH)6]3−, CrMo6) anion exhibiting emission derived from Cr3+ was utilized with n-dodecylammonium ([C12H25NH3]+, C12NH3) surfactant cation to obtain a photoluminescent hybrid crystal. The grown single crystal of C12NH3-CrMo6 comprised a distinct layered structure consisting of inorganic CrMo6 layers and interdigitated C12NH3 layers. In the CrMo6 layers, the CrMo6 anions were associated with water molecules by hydrogen bonding to form a densely packed two-dimensional network. Steady-state and time-resolved photoluminescence spectroscopy revealed that the C12NH3-CrMo6 hybrid crystal exhibited characteristic emission from the CrMo6 anion. Preliminary lasing properties were also observed for C12NH3-CrMo6, which shows the possibility of using the C12NH3-CrMo6 hybrid crystal as an inorganic–organic hybrid laser.

This study explores the influence of temperature–time conditions, surfactants, and varied waste compositions on the curing of geopolymer gels, a foam formation with the properties of porous geopolymers. Findings reveal that a 6 h curing period leads to a density of 435 kg/m3 and strength of 0.66 MPa, with notable improvements at 12 h. Comparing 12 to 24 h curing, differences in characteristics remain within 5%, highlighting the 12 h period as more energy-efficient. Sodium stearate-based samples exhibit excellent properties, significantly boosting strength while maintaining overall properties. Microwave curing achieves the lowest density (291 kg/m3) and closely parallels properties of samples cured conventionally for 12 h. However, it leads to complete destruction in sodium stearate-modified gels due to the Dumas reaction, making it unsuitable above 200 °C. Optimal properties emerge from compositions using sodium stearate and oven curing, achieving densities of 334 kg/m3 and strengths of 1.08 MPa (Severodvinsk CHPP-1) and 373 kg/m3 and 1.17 MPa (Novocherkassk SDPP). Although microwave curing allows for high energy efficiency, its high temperature demands necessitate careful material selection. This study offers insight into enhancing geopolymer properties while emphasizing the importance of tailored curing methods for sustainable material development.

Objectives. The influence of the technological additive content and accelerated aging conditions on the surface energy and elastic-strength properties of nitrile butadiene rubbers with an average acrylic acid nitrile content and rubbers based on them were studied in the paper.Methods. The free surface energy of the samples was determined under the standard conditions and in the accelerated aging conditions with the use of the Owens, Wendt, Rabel, and Kaelble method.Results. It was shown that the elastomeric materials surface energy is influenced by surfactants such as rosin and stearic acid, which are typical ingredients of rubber compounds. It was also found that the thermal aging effect on the physical and mechanical properties of rubbers based on nitrile butadiene rubbers depends on the method of rubber isolation from latex and on the nature of the surfactant components in the samples.Conclusions. The analysis of the results obtained shows that the change in the vulcanizates physical and mechanical properties, depending on the technological additive content and the temperature effect, occurs along with a change in the critical surface tension.

In this study, we discovered that washing hair with surfactants causes a decrease in the internal density of hair, and we propose a cuticle-sealing strategy to inhibit this phenomenon. This phenomenon was revealed based on optical analyses such as optical microscopy, scanning electron microscopy (SEM), drop shape analysis, atomic force microscopy (AFM), and single hair analysis. Repeated treatment with surfactants creates areas of low density within the hair. Additionally, treatment with low-molecular-weight materials resulted in replenishment of the internal density of the hair. It has been shown that the more severe the degree of cuticle lifting, the more the internal density of the hair is reduced by surfactants. In addition, the study confirmed that a decrease in internal density could be prevented by sealing the cell membrane complex (CMC), and it was suggested that this reduced internal density may reflect the pore structure of hair. This study investigates the mass transfer phenomenon that occurs in hair and proposes a strategy to maintain hair homeostasis.

In this study, a novel and environmental strategy is reported for multicomponent synthesis of pyrrole derivatives in water. We prepare and characterize Fe3O4@CTAB-SDS@Cu2+-Ag+ as a double surfactant-modified magnetic nanocatalyst. We compare catalytic activity of this catalyst with a mono surfactant-modified catalyst in the synthesis of pyrroles. It seems that the addition of Sodium dodecyl sulfate (SDS) as cosurfactant provides better stabilization of the emulsion and leads to the production of adhesive emulsions by the formation of a bilayer. On the other hand, surface decoration of SDS by Cu2+ and Ag+ improves catalytic activity. The magnetic nanocomposite was characterized by TEM, EDS, XRD, VSM and FT-IR techniques and the structure of the synthesized pyrrole was confirmed by FT-IR, 1H NMR and 13C NMR.

Foam fluids are widely used in petroleum engineering, but long-standing foam stability problems have limited the effectiveness of their use. The study explores the synergistic effects and influencing factors of SiO2 nanoparticles (SiO2-NPs) with different wettability properties and three different surfactants. The paper investigates the foaming performance of different types of surfactants and analyzes and compares the stability of foam after adding hydrophilic and hydrophobic SiO2-NPs from macroscopic as well as microscopic perspectives, and the effects of temperature and inorganic salts on the stability of mixed solutions. The experimental results show that: 1) hydrophilic nanoparticles can significantly enhance the foam stability of amphoteric surfactants, with a small increase in the foam stability of anionic and cationic surfactants; 2) The concentration of nanoparticles did not have a significant effect on the stability of the cationic surfactants and this conclusion was verified in the experimental results of the surface tension measured below;3) The cationic surfactants showed better temperature resistance at temperatures of 50–90 °C. Both amphoteric surfactant solutions with the addition of hydrophilic SiO2-NPs or hydrophobic SiO2-NPs significantly improved the temperature resistance of the foam at high temperatures. The anionic surfactant solution with hydrophobic SiO2-NPs did not enhance the solution temperature resistance; 4) The surface tension of the surfactant solution gradually increases with increasing concentration of hydrophilic or hydrophobic SiO2-NPs and then levels off; 5) the hydrophilic SiO2-NPs had a significant effect on the salt tolerance of the anionic and amphoteric surfactant solutions. The salt tolerance of cationic surfactant solutions with hydrophobic SiO2-NPs was better than that of surfactants with hydrophilic SiO2-NPs.

In this study, the micellization behavior of the sodium cholate (SCH) and sodium dodecyl sulfate (SDS), in aqueous solution in pure state, and mixture of them (SCH + SDS) in different mole fractions were investigated by conductometric method at 298.15 K. The obtained data from experimental measurements were used to determination of the critical micelle concentration (CMC) of surfactants in pure and mixed state. Also according to Regular Solution Theory (RST), were calculated the following parameters: the interaction parameter between surfactants in the mixed system ( ), activity coefficient ( ، ), mole fractions of the components in the mixed micelle ( , ) and thermodynamic parameters such as Gibbs free energy of micellization ( ) and excess free energy ( ). The results obtained show that in the anionic-anionic mixture, the interaction parameter is low and the activity coefficients show a small deviation from the ideal state, the standard Gibbs free energy of micellization ( ) are negative values, this shows that the micelle formation process take place spontaneously.

The oil and gas industry is often challenged with serious problems like high cost of oil field chemicals and environmental toxicity issues of commonly used synthetic oil field chemicals, and this has dragged the attention of researchers to the search for more cost effective and environmentally friendly oil field chemicals. Oil field chemicals formulated from various renewable sources (such as plant extracts) have been recognized as an alternative with great environmental advantages, cost advantage, and availability compared to their synthetic counterparts. Cashew nut shell liquid (CNSL), a byproduct of the cashew industry, stands out as a unique renewable starting material amongst others due to its peculiar structural feature, low cost, and availability. It consists of naturally occurring substituted phenolic compounds that can participate in diverse reactions for the manufacture of numerous useful products. A large number of chemicals and products have been developed starting from CNSL by taking advantage of the reactive sites namely phenolic hydroxyl, aromatic ring, the acid functionality, and unsaturation(s) in the C15 alkyl side chain. This update gives highlights on the composition, extraction, isolation, and reactivity of CNSL. It also focuses on the oil field application of CNSL and its derivatives.

Studies show that after acidizing operation of oil wells using the alkali/surfactant/polymer (ASP) flooding technology, the produced fluid is emulsified. Since the produced emulsion is stable, it affects the oil–water separation performance. In order to analyze the generation of stable emulsion in the produced fluid after acidizing an oil well, innovative separation experiments were carried out on real oil wells. During the experiments, solid particles in the middle layer of the emulsifying system in the produced fluid after acidizing ASP flooding were extracted and characterized. The generation of the stable emulsifying system in the produced fluid was studied through stability experiments and molecular dynamics simulations. The results showed that the synergistic effect of ferrous sulfide nanoparticles and surfactants was the fundamental reason for the strong emulsifying stability of the produced liquid after acidizing of the ternary composite system. The generation of ferrous sulfide solid particles mainly included two steps. First, sulfate reducing bacteria in injected water by ASP flooding reacted with sulfate in formation water to form hydrogen sulfide. Then, the hydrogen sulfide reacted with iron metal in oil wells and casing of wellbore to form ferrous sulfide particles. It was found that surfactants are adsorbed on the surface of ferrous sulfide nanoparticles. Subsequently, the control ability of surfactant on oil and water phases in the liquid film was enhanced. The performed analyses demonstrate that the adsorption of solid particles to the oil phase was enhanced, while the free motion of molecules in the oil phase at the liquid film position was weakened. The strength of the interfacial film between oil and water was further increased by the synergistic effect of ferrous sulfide nanoparticles and surfactant. The present study is expected to provide a guideline for a better understanding of the efficient treatment of produced fluids in ASP flooding.

In many modern technologies, surface-active compounds, such as surfactants, polymers, proteins, particles and their mixtures, are essential components. They change the dynamic and equilibrium properties of the inherent interfaces, which is mostly visible in foams and emulsions. The interfacial dilational visco-elasticity is probably the most informative quantity due to its direct interrelation to the equation of state of the corresponding interfacial layers as well as the mechanisms governing the interfacial molecular dynamics. The scientific field of interfacial visco-elasticity, although quite young, has been inspired by the pioneering work of Marangoni, Levich, Lucassen, Lucassen-Reynders, Hansen, van den Tempel and Krotov, and during the last decades, also significantly by Boris Noskov. His contributions to the theoretical foundation and experimental analysis of polymer and mixed surfactant–polymer interfacial layers in particular are essential.

Chelating agents’ application for well stimulation is gaining more and more interest, as they can perform under harsh conditions. However, the mutual influence of surfactants and chelating agents on the wettability alteration of hydrophobic carbonate rock under conditions of high-temperature well stimulation is relatively unexplored. This paper aims to study interfacial processes on the surface of hydrophobic rock in the presence of the EDTA-based chelating agent and surfactants of different classes. Cationic (cetyltrimethylammonium bromide, CTAB, and cetylpyridinium bromide, CPB), anionic (sodium dodecyl sulfate, SDS), and amhoteric (alkyldimethyl aminooxide, AO) surfactants were studied. Wettability alteration of model hydrophobic rock was studied under conditions specific to well stimulation. It was shown that chelating agent (CA) alone and its mixture with SDS could not lead to sufficient wettability alteration. CTAB, CPB, and AO were able to change the wettability effectively. A synergistic effect between CA and these surfactants was observed and a possible mechanism was proposed. AO was selected as the most promising surfactant. The influence of surfactant on the CA’s dissolution capacity towards carbonate rock was investigated; dissolution capacity strongly depends on wettability alteration. Finally, the effect of CA, AO, and their mixture on the wettability of aged reservoir rock was studied and the absence of negative effects was proven.

The assembly of colloidal hyaluronic acid (HyA, as a polysaccharide) based hydrogel particles in an aqueous medium is characterized in the present paper, with an emphasis on the particular case of nanohydrogels formed by surfactant-neutralized polysaccharide networks. The structural changes and particle formation process of polysaccharide- and cationic-surfactant-containing systems were induced by the charge neutralization ability and the hydrophobic interactions of cetyltrimethylammonium bromide (CTAB) under different conditions. Based on the rheological, light scattering, ζ-potential, turbidity, and charge titration measurements, it can be concluded that the preparation of the HyA-CTAB particles can be greatly controlled. The results indicate that more available negative charges can be detected on the polymer chain at smaller initial amounts of HyA (cHyA < 0.10 mg/mL), where a molecular solution can be formed. The change in the pH has a negligible effect on the formation process (particle aggregation appears at nCTAB/nHyA,monomer~1.0 in every case), while the temperature dependence of the critical micelle concentration (c.m.c.) of CTAB determines the complete neutralization of the forming nanohydrogels. The results of our measurements confirm that after the appearance of stable colloidal particles, a structural change and aggregation of the polymer particles take place, and finally the complete charge neutralization of the system occurs.

Liposomes modified with tetradecyltriphenylphosphonium bromide with dual loading of α-tocopherol and donepezil hydrochloride were successfully designed for intranasal administration. Physicochemical characteristics of cationic liposomes such as the hydrodynamic diameter, zeta potential, and polydispersity index were within the range from 105 to 115 nm, from +10 to +23 mV, and from 0.1 to 0.2, respectively. In vitro release curves of donepezil hydrochloride were analyzed using the Korsmeyer–Peppas, Higuchi, First-Order, and Zero-Order kinetic models. Nanocontainers modified with cationic surfactant statistically better penetrate into the mitochondria of rat motoneurons. Imaging of rat brain slices revealed the penetration of nanocarriers into the brain. Experiments on transgenic mice with an Alzheimer’s disease model (APP/PS1) demonstrated that the intranasal administration of liposomes within 21 days resulted in enhanced learning abilities and a reduction in the formation rate of Aβ plaques in the entorhinal cortex and hippocampus of the brain.

This work presented the production and incorporation of calcium-hydrolyzed nano-solutions at three concentrations (1, 2, and 3 wt.%) in alkali-activated gold mine tailings (MTs) from Arequipa, Perú. As the primary activator solution, a sodium hydroxide (NaOH) solution at 10 M was used. Calcium-hydrolyzed nanoparticles with a particle size of 10 nm were localized inside self-assembled molecular spherical systems (micelles) with diameters of less than 80 nm that were well-dispersed in aqueous solutions and acted as secondary activator, and also as additional calcium resource for alkali-activated materials (AAMs) based on low-calcium gold MTs. High-resolution transmission electron microscopy/energy-dispersive X-ray spectroscopy (HR-TEM/EDS) analyses were carried out to characterize the morphology, size, and structure of the calcium-hydrolyzed nanoparticles. Fourier transform infrared (FTIR) analyses were then used to understand the chemical bonding interactions in the calcium-hydrolyzed nanoparticles and in the AAMs. Scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS) and quantitative X-ray diffraction (QXRD) were performed to study the structural, chemical, and phase compositions of the AAMs; uniaxial compressive tests evaluated the compressive strength of the reaction AAMs; and nitrogen adsorption–desorption analyses measured porosity changes in the AAMs at the nanostructure level. The results indicated that the main cementing product generated was amorphous binder gel with low quantities of nanostructured C-S-H and C-A-S-H phases. The surplus production of this amorphous binder gel produced denser AAMs at the micro-level and nano-level (macroporous systems). In addition, each increase in the concentration of calcium-hydrolyzed nano-solution had a direct/proportional effect on the mechanical properties of the AAM samples. AAM with 3 wt.% calcium-hydrolyzed nano-solution had the highest compressive strength, with a value of 15.16 MPa, which represented an increase of 62% compared with the original system without nanoparticles that were aged under the same conditions at 70 °C for seven days. These results provided useful information about the positive effect of calcium-hydrolyzed nanoparticles on gold MTs and their conversion into sustainable building materials through alkali activation.

Surfactants exhibit many inherent properties, one of the properties is their favorable capacity to absorb at the interface or surface in which surfactant molecules are transferred from bulk phase of solution to the interface. With the evolution in the synthesis routes of nanoparticles (NPs) via colloidal chemistry approaches, now the adsorption capacity of surfactants is being exploited concerning the stabilization of the NPs. In present research work, colloidal mercuric sulfide nanoparticles (HgS NPs) have been synthesized with effective sizes below 15 nm in aqueous solutions of various surfactants through facile chemical precipitation technique. Different head groups and hydrophobic chain length moieties have been tested for various cationic and anionic surfactants. These surfactants have been demonstrated to produce dispersed spherical configured HgS NPs, in which the composition of surfactant has controlled growth assessment. Although, the NPs in the pulverized form exhibit β-HgS form except of the surfactant opted. Surfactant adsorption at the surface of NP has been shown due to change in inter-particle potential and prevents the self-aggregation of NPs. Additionally, it has been demonstrated that the surfactants (stabilizers) have some favorable chemical moiety which promotes the binding at NP surface, generates an adequate size of particles and eventually inhibits their unlimited growth. The kinetics of nucleation and growth of surfactant stabilized HgS NPs follows the first-order rate law in all the surfactants. However, the first order rate constant has shown prominent surfactant dependence.

This study aims to determine the effect of sea sand modification with SDBS for adsorption of Fe3+. Sea sand was treated with 0.1 M HCl solution at 25oC. Organo-quartz was prepared at SDBS concentration of below, equal, and above the CMC value by shaking the mixture for 4 hours at 100 rpm. Characterization by FTIR spectrophotometry showed a change in the spectra pattern. The activation caused increasing of -OH silanol while modifications make them decrease. Characterization with SEM showed that the morphology of the sea sand was not uniform with irregular white chunks. The EDX results showed that the dominant elements were C (13.89% ± 10.86), O (40.48% ± 6.58), Si (16.51% ± 8.13), and Fe (11.68% ± 14.38). Adsorption was carried out using Fe3+ at 50 ppm. The Fe3+ analysis was conducted by AAS. The adsorption value by activated sea sand was 58.22% ± 7.23% whereas without treatment sea sand was 70.46% ± 5.54, and the modified sea sand was 53.24% ± 4.86. The lower adsorption is probably caused by the dissolved iron oxides in sea sand during activation.

Photo-Fenton oxidation is one of the most efficient advanced oxidation process that is used for the treatment of effluents containing recalcitrant compounds. In this research, the removal of an anionic surfactant, sodium dodecyl sulfate, by MnFe2O4/ZnO nanocatalyst using photo-Fenton advanced oxidation process has been investigated. In this study, the MnFe2O4/ZnO nanocomposite was firstly synthesized and characterized, and then applied in the photo-Fenton oxidation process under UV irradiation. The effect of different parameters, such as pH, catalyst dose and the amount of hydrogen peroxide, on the process were investigated. Under the optimum conditions, at pH = 7, with a surfactant concentration of 5 mg/L, at 30 min using 2.24 mL hydrogen peroxide, the surfactant removal efficiency was 100%. The results show that the proposed method using the synthesized nanocatalyst has a high efficiency in the removal of surfactants.

Coarse-grained molecular dynamics simulations that incorporate explicit water-mediated hydrophilic/hydrophobic interactions are employed to track spatiotemporal evolution of diblock copolymer aggregation in initially homogeneous solutions. A phase portrait of the observed morphologies and their quantitative geometric features such as aggregation numbers, packing parameters, and radial distribution functions of solvent/monomers are presented. Energetic and entropic measures relevant to self-assembly such as specific solvent accessible surface area (SASA) and probability distribution functions (pdfs) of segmental stretch of copolymer chains are analyzed. The simulations qualitatively capture experimentally observed morphological diversity in diblock copolymer solutions. Topologically simpler structures predicted include spherical micelles, vesicles (polymersomes), lamellae (bilayers), linear wormlike micelles, and tori. More complex morphologies observed for larger chain lengths and nearly symmetric copolymer compositions include branched wormlike micelles with Y-shaped junctions and cylindrical micelle networks. For larger concentrations, vesicle strands, held together by hydrogen bonds, and “giant” composite aggregates that consist of lamellar, mixed hydrophobic/hydrophilic regions and percolating water cores are predicted. All structures are dynamic and exhibit diffuse domain boundaries. Morphology transitions across topologically simpler structures can be rationalized based on specific SASA measurements. PDFs of segmental stretch within vesicular assemblies appear to follow a log-normal distribution conducive for maximizing configuration entropy.

MnZn ferrite precursor powders were prepared by the nano in situ composite method. Three surfactants, which include polyethylene glycol 400 (PEG-400), cetyltrimethyl ammonium bromide (CTAB), and sodium dodecyl sulfate (SDS), were usedM and the impact of the surfactants on the precursor sol solutions and precursor powders was studied. X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, a field emission scanning electron microscope (FE-SEM), a transmission electron microscope (TEM), a Zeta potential meter, a BET surface analyzer, and a vibrational sample magnetometer (VSM) were used to characterize the precursor sol solutions and the precursor powders. The results showed that these surfactants can improve the dispersion state and Zeta potentials of sol particles and increase the specific surface areas of the precursor powders. Moreover, the precursor powders were composed of MnZn ferrite, and some were amorphous. CTAB was the optimum surfactant and the zeta potential of the sol particles and the specific surface area of the precursor powders named P-0.1CTAB are 10.7 mV and 129.07 m2/g, respectively. In addition, the nano-particles that were made up of the P-0.1CTAB precursor powders had smaller sizes and more uniform particle distributions than the others. The magnetic properties’ improvement was attributed to the addition of surfactants, and CTAB is the optimal type. In addition, the novel nano in situ composite method will inspire fresh thinking and investigation into the research of ferrite.

The high fluidity and low yield stress of fresh foam concrete affect the shape stability and buildability of foam concrete in the printing process, which is quite a challenge to its application in digital construction. Therefore, this article proposes the preparation and characteristics of 3D printed pre-foaming concrete (3DFC). The rheological properties proved that the addition of 0.1 wt.% Hydroxypropyl methyl cellulose (HPMC) to 3DFCs weakens the fluidity but increases the static yield stress and apparent viscosity, thus enhancing the buildability. More importantly, the influences of surfactant on the rheological property, compressive strength, pore structure and thermal conductivity of 3DFCs were evaluated. Analysis results show that the static yield stress of 3DFCs decreases from 1735 to 687 Pa with surfactant dosage from 0 to 2 wt.%. Moreover, the addition of surfactant significantly reduced the apparent viscosity of 3DFCs (especially at low shear rates), but its viscosity recovery rate was basically unchanged, which is good for buildability. Thanks to the increase of porosity, the volume density of 3DFCs decreased from 2211 to 1159 kg/m3, but the compressive strength of 3DFCs also decreased slightly. The thermal conductivity of 3DFCs shows good thermal insulation performance in the range of 0.2254–0.2879 W/m·K, which is also due to the increase in porosity of 3DFCs. Finally, in order to verify the practical application value of 3DFCs, an industrial printing product with more than 30 layers during the field application is displayed.

Objectives. This study was aimed at the investigation of the supramolecular systems based on cationic surfactants bearing cyclic head groups (imidazolium and pyrrolidinium) and polyanions (polyacrylic acid (PAA) and human serum albumin (HSA)), and factors governing their structural behavior to create functional nanosystems with controlled properties. Research hypothesis. Mixed PE–surfactant complexes based on oppositely charged species are characterized by multifactor behavior strongly affected by the nature of both components. It was expected that the transition from a single surfactant solution to an admixture with PE might provide synergetic effects on structural characteristics and functional activity. To test this assumption, the concentration thresholds of aggregation, dimensional and charge characteristics, and solubilization capacity of amphiphiles in the presence of PEs have been determined by tensiometry, fluorescence and UV-visible spectroscopy, and dynamic and electrophoretic light scattering. Results. The formation of mixed surfactant–PAA aggregates with a hydrodynamic diameter of 100–180 nm has been shown. Polyanion additives led to a decrease in the critical micelle concentration of surfactants by two orders of magnitude (from 1 mM to 0.01 mM). A gradual increase in the zeta potential of HAS–surfactant systems from negative to positive value indicates that the electrostatic mechanism contributes to the binding of components. Additionally, 3D and conventional fluorescence spectroscopy showed that imidazolium surfactant had little effect on HSA conformation, and component binding occurs due to hydrogen bonding and Van der Waals interactions through the tryptophan amino acid residue of the protein. Surfactant–polyanion nanostructures improve the solubility of lipophilic medicines such as Warfarin, Amphotericin B, and Meloxicam. Perspectives. Surfactant–PE composition demonstrated beneficial solubilization activity and can be recommended for the construction of nanocontainers for hydrophobic drugs, with their efficacy tuned by the variation in surfactant head group and the nature of polyanions.

The aim of this study was to evaluate the performance of a reverse osmosis (RO) membrane in surfactant removal using various surfactant model aqueous solutions. The separation tests were performed with laboratory scale units in a dead-end configuration. Cellulose Acetate (CA) and Polyamide (PA) RO membranes were used with nonionic, anionic, or cationic surfactants at a wide range of concentrations. Membrane performance was evaluated using permeate flux and total organic carbon (TOC) rejection. The effects of surfactant type and concentration on RO membranes were assessed. Permeate flux of the PA membrane depended on the surfactant type and concentration. The separation of cationic surfactant aqueous solutions yielded the lowest permeate flux, followed by nonionic and anionic surfactant aqueous solutions, respectively. Surfactant adsorption on the membrane surface occurred at very low concentration of cationic and nonionic surfactants due to electrostatic and hydrophobic interactions, respectively, which affected permeate flux, and micelles did not affect the permeate flux of PA membrane. However, for CA membrane the permeate flux was not affected by the feed solution. Both membranes exhibited satisfactory TOC rejection (92–99%). This study highlights the importance of assessing interactions between membrane material and surfactant molecules to mitigate membrane fouling and guarantee a better performance of the RO membrane.

The surface microstructure of a catalyst coating layer directly affects the active area, hydrophilicity and hydrophobicity, and the high porosity is desirable especially for solid–liquid–gas three-phase catalytic reactions. However, it remains challenging to customize catalyst distribution during the coating process. Here, we report a simple strategy for achieving ultrafine nanocatalyst deposition in a porous structure via introducing the surfactant into coating inks. For a proof-of-concept demonstration, we spin-coated the nanoscale IrO2 sol with a surfactant of sodium dodecyl sulfate (SDS) onto the glassy carbon (GC) electrode for oxygen evolution reaction (OER). Due to the surfactant action, the deposited IrO2 nanocatalyst is evenly distributed and interconnected into a highly porous overlayer, which facilitates electrolyte permeation, gas bubble elimination and active-site accessibility, thus affording high-performance OER in alkaline media. Particularly, the SDS-modified electrodes enable the industrial-level high-current-density performance via enhanced mass transfer kinetics. Such manipulation is effective to improve the coating electrodes’ catalytic activity and stability, and scalable for practical applications and suggestive for other gas-evolving electrodes.

Several approaches quantitatively describe the effect of surfactant micellar solution on the reaction rate. The most used among them are Piszkiewicz’s, Berezin’s, and Pseudophase Ion-Exchange (PIE) models. The last-named was developed by Bunton and Romsted. Piszkiewicz’s model is based on representations of the micellization according to the mass action law with the formation of a catalytic micelle, which consists of some surfactant molecules and a substrate. In our previously paper, this model was used to explain the kinetic micellar effect on the reaction of cationic triphenylmethine dyes with water once again showed the main disadvantages of this approach. Berezin’s model is based on another model of micelle formation viz. the pseudophase model, and the binding of reagents by micelles is considered as the distribution of a substance between two phases. In this work, we aim to consider the applicability of Berezin’s approach for the interaction of malachite green and brilliant green cations with water molecule as a nucleophile in aqueous systems of nonionic, anionic, cationic, and zwitterionic surfactants. On the whole, Berezin's model performed well when applied to the description of the micellar effect on the reaction of similar dye with the hydroxide ion. However, it was revealed that this model does not take into account the change in the local concentration of the HO– ions due to a compression of the double electric layer upon addition of reacting ions to the system, as well as the constant of association of the HO– ions with cationic head groups of surfactant. In this case, when water is used as a nucleophile, the question of the degree of nucleophile binding can be solved differently. The PIE model is also based on a pseudophase model of micellization, but a substrate binding by micelles is considered as an association in a stoichiometric ratio of 1:1, and a nucleophile concentration is expressed in a local concentration based on the neutralization degree of micelles. Given the latter, its approach cannot be applied to the kinetic micellar influence on the reaction of cationic triphenylmethine dyes with water.

Permanent red 24 (1-(2,4-Dinitro-phenylazo)-naphthalen-2-ol) is a family member of azo dyes. Azo dyes have so many industrial applications. In this study, permanent red 24 nano pigments were prepared by microemulsion as a novel method. The effects of different experimental parameters for nano pigment preparation were studied. The investigated parameter include surfactant nature, solvent, surfactant, cosurfactant, and pigment percentage in microemulsion formulation. Optimal formulation determined for nano pigment preparation. Performing the process under the optimal formulation leads to the production of nano pigment with an average size of about 85 nm. The nano pigment was characterized by Transmission Electron Microscopy (TEM) and Dynamic Light Scattering (DLS). The DLS measurements confirm TEM analysis.