Search Results (257)

The stability of nitrogen gas foam hinders its applicability in petroleum applications. Fly ash nanoparticles and clay improve the N₂ foam stability, and flue gas foams provide a cost-effective solution for carbon capture, utilization, and storage (CCUS). This study examines the stability, volume, and bubble structure of foams formed using two anionic surfactants, sodium dodecyl sulfate (SDS) and sodium dodecylbenzene sulfonate (SDBS), along with the cationic surfactant cetyltrimethylammonium bromide (CTAB), selected for their comparable interfacial tension properties. Analysis of foam stability and volume and bubble structure was conducted under different CO₂/N₂ mixtures, with half-life and initial foam volume serving as the evaluation criteria. The impact of fly ash and clay on SDS-N₂ foam was also evaluated. The results showed that foams created with CTAB, SDBS, and SDS exhibit the greatest stability in pure nitrogen, attributed to low solubility in water and limited gas diffusion. SDS showed the highest foam strength attributable to its comparatively low surface tension. The addition of fly ash and clay significantly improved foam stability by migrating to the gas–liquid interface, creating a protective barrier that reduced drainage. Both nano fly ash and clay improved the half-life of nitrogen foam by 11.25 times and increased the foam volume, with optimal concentrations identified as 5.0 wt% for fly ash and 3.0 wt% for clay. This research emphasizes the importance of fly ash nanoparticles in stabilizing foams, therefore optimizing a foam system for enhanced oil recovery (EOR). Full article

Commercially available bismuth subcarbonate (Bi₂O₂CO₃) was treated with nitric acid and the surfactant cetyltrimethylammonium bromide. The treated catalysts exhibited enhanced photocatalytic activity compared to pure Bi₂O₂CO₃ in the decolorization of rhodamine B (RhB) under visible light irradiation. The absorbance at 554 nm gradually decreased over time and disappeared completely within 80 min. The crystal structure, morphology, and optical properties of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The improved photocatalytic activity of the treated catalysts was attributed to partial carbonate removal and the formation of Bi⁵⁺ species. Scavenger experiments indicated that superoxide radicals (·O₂⁻) and photogenerated holes (h⁺) played significant roles in the photocatalytic decolorization of RhB. Full article

Due to widespread use of silver nanoparticles (AgNPs), the assessment of their potential harm to microalgal photosynthesis is crucial, as microalgae, together with cyanobacteria, contribute to approximately 50% of global oxygen production. This study investigated photosynthetic pigments, photosynthetic rate, chlorophyll a fluorescence, and the expression of photosynthesis-related genes and proteins in green alga Chlorella vulgaris after 72 h exposure to citrate- and cetyltrimethylammonium bromide (CTAB)-stabilized AgNPs, as well as silver ions (AgNO₃), at concentrations allowing 75% cell survival (EC₂₅). All treatments impaired photosynthetic performance. The most pronounced decreases in chlorophyll fluorescence parameters and photosynthetic rate, alongside elevated energy dissipation, were observed after exposure to AgNP-CTAB and AgNO₃. AgNP-citrate had milder effects and induced compensatory responses, reflected in an increased performance index and upregulation of photosynthesis-related proteins. AgNP-CTAB induced the strongest downregulation of gene and protein expression, likely due to its higher EC₂₅ concentration and cationic surface promoting interaction with photosynthetic structures. Although AgNO₃ caused fewer molecular changes, it significantly disrupted photosynthetic function, suggesting a direct effect of Ag⁺ ions on photosynthesis-related proteins. Overall, the results highlight the role of AgNPs’ surface coatings and dosage in determining their phytotoxicity, with photosystem disruption and oxidative stress emerging as key mechanisms of action. Full article

This study centers on the adsorption–flotation coupling extraction of rubidium (Rb⁺) and cesium (Cs⁺) within a titanium silicate (CTS)–cetyltrimethylammonium bromide (CTAB) system, systematically investigating the impacts of pH, aeration rate, CTAB concentration, and flotation time on the extraction efficiency of these elements. Single-factor experiments revealed that the optimal flotation efficiency was achieved when the pH ranged from 6 to 10, the aeration rate was set at 1000 r/min, the CTAB concentration was 0.2 mmol/L, and the flotation duration was 18 min. Under these conditions, the adsorption capacities for Rb⁺ and Cs⁺ were recorded as 128.32 mg/g and 185.47 mg/g, respectively. Employing the response surface optimization method to analyze the interactive effects of these four factors, we found that their order of significance was as follows: pH > aeration rate > CTAB concentration > flotation time. The optimized parameters were determined as pH 8.64, bubble formation rate 1121 r/min, CTAB concentration 0.26 mmol/L, and flotation time 18.47 min. Under these refined conditions, the flotation efficiency for both CTS–Rb and CTS–Cs surpassed any single-factor experiment scenario, with the flotation efficiencies for Rb⁺ and Cs⁺ reaching 95.05% and 94.82%, respectively. This methodology effectively extracts Rb⁺ and Cs⁺ from low-concentration liquid systems, while addressing the challenges of solid–liquid separation for powdered adsorption materials. It holds significant theoretical and practical reference value for enhancing the separation processes of low-grade valuable components and boosting overall separation performance. Full article

Cu-based nanomaterials have received considerable attention as promising and cost-effective substrates for surface-enhanced Raman spectroscopy (SERS) applications despite their relatively low enhancement factor (EF) compared to noble metals like gold and silver. In this study, a fast and affordable synthesis route is proposed to obtain a three-dimensional porous copper film (NPC) via an electrodeposition technique based on the dynamic hydrogen bubbling template (DHBT). Two sets of NPC film were synthesized, one without additives and the other with cetyltrimethylammonium bromide (CTAB). The impacts of deposition time on the NPCs’ porous morphology, thickness, and SERS performance were systematically investigated. With the optimal deposition time, the nanopore sizes could be tailored from 26.8 to 73 μm without additives and from 12.8 to 24 µm in the presence of CTAB. The optimal additive-free NPC film demonstrated excellent SERS performance at 180 s of deposition, while the CTAB-modified film showed strong enhancement at 120 s towards methylene blue (MB), a highly toxic dye, achieving a detection limit of 10⁻⁶ M. Additionally, the samples with CTAB showed better efficiency than those without CTAB. The calculated EF of NPC was found to be 5.9 × 10³ without CTAB and 2.5 × 10³ with the CTAB, indicating the potential of NPC as a cost-effective candidate for high-performance SERS substrates. This comprehensive study provides insights into optimizing the structural morphology of the NPCs to maximize their SERS enhancement factor and improve their detection sensitivity toward MB, thus overcoming the limitations associated with conventional copper-based SERS substrates. Full article

This study prepared epoxy–clay nanocomposites (ECNs) by incorporating organophilic clays modified with either non-redox cetyltrimethylammonium bromide (CTAB) or redox-active aniline pentamer (AP), then compared their anticorrosion performance on metal substrates in saline environments. The test solution contained 2 wt% alkaline copper quaternary (ACQ) wood preservatives. Cold-rolled steel (CRS) panels coated with the ECNs were evaluated via electrochemical impedance spectroscopy (EIS) in saline media both with and without ACQ. For CRS coated with unmodified epoxy, the Nyquist plot showed impedance dropping from 255 kΩ to 121 kΩ upon adding 2 wt% ACQ—indicating that Cu²⁺ ions accelerate iron oxidation. Introducing 1 wt% CTAB–clay into the epoxy increased impedance from 121 kΩ to 271 kΩ, while 1 wt% AP–clay raised it to 702 kΩ. This improvement arises because the organophilic clay platelets create a more tortuous path for Cu²⁺ and O₂ diffusion, as confirmed by ICP–MS measurements of Cu²⁺ after EIS and oxygen permeability tests (GPA), thereby slowing iron oxidation. Moreover, ECN coatings containing AP–clay outperformed those with CTAB–clay in corrosion resistance, suggesting that AP not only enhances platelet dispersion but also promotes formation of a dense, passive metal oxide layer at the coating–metal interface, as shown by TEM, GPA, and XRD analyses. Finally, accelerated salt-spray exposure following ASTM B-117 yielded corrosion behavior consistent with the EIS results. Full article

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

Studying the wettability of plant growth regulators on crop leaf surfaces is essential for enhancing crop yield. In this study, the wetting behavior of the plant growth regulator 28-homo-brassinolide (28-HB), supplemented with different surfactants, was investigated on the adaxial and abaxial surfaces of pepper leaves at the seedling, early flowering, and fruiting stages. The microstructure of the leaf surface was characterized using an ultra-depth field microscope. The surface free energy (SFE) of the leaves was calculated using the Owens-Wendt-Rabel-Kaelble (OWRK) method. Additionally, the surface tension of the 28-HB solutions containing various surfactants, as well as the contact angles on pepper leaves at different growth stages, were measured. The experimental results indicate that the surface free energy (SFE) of pepper leaves significantly decreases with plant maturation. Specifically, the SFE of the adaxial leaf surface declined from 43.4 mJ/m² at the seedling stage to 26.6 mJ/m² at the fruiting stage, while the abaxial surface decreased from 27.5 mJ/m² to 22.5 mJ/m². At all growth stages, the relative polar component (R_P) of the adaxial surface was consistently higher than that of the abaxial surface and showed a gradual decline from 94.70% to 57.34% as development progressed. The contact angle measurement showed that the addition of surfactant decreased the contact angle of 28-HB on the leaf surface and increased the wetting area. Among the tested formulations, the addition of fatty alcohol ethoxylates (AEO-9) significantly reduced the contact angle to below 45°, and resulted in an adhesion tension below 30 mN/m and adhesion work lower than 105 mJ/m². These values indicate superior wetting performance compared to formulations containing sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB). This study integrates the surface free energy characteristics of pepper leaves at different growth stages with the wetting performance of various surfactant systems, providing a quantitative basis for the selection and optimization of surfactants in agricultural spray formulations. The findings offer theoretical support for precise pesticide application strategies, enhancing pesticide adhesion and absorption on leaf surfaces, thereby improving pesticide utilization efficiency throughout the crop growth cycle. Full article

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

Per- and polyfluoroalkyl substances (PFASs) are a family of synthetic chemicals that were used to improve the quality of several commercial products by making them resistant to heat, oil, stains, and grease. By containing a fluorinated carbon tail and a hydrophilic head (-COOH, -SO₃H), PFASs act as surfactants that are attracted to bubble–water interfaces. Foam fractionation is the process of facilitating PFAS–air bubble interactions for the purpose of removing contaminants from tainted water. In this paper, we report on the use of foam fractionation and electrochemical oxidation (EO) under stirred batch conditions (200 mL) to remediate PFAS-contaminated water. We used radiolabeled PFOA (perfluorooctanoic acid; ¹⁴C-PFOA) as a representative surrogate to quickly screen treatment variables of flow rate, pH, temperature, and soap mass. Using radiolabeled PFASs eliminated the possibility of cross-contamination and greatly reduced analytical costs and processing time. The results showed that foam fractionation can remove 80 to 90 percent of PFOA from water within 30 min and that 90 to 100 percent of the PFOA in the concentrated foamate can be oxidized via electrochemical oxidation (-¹⁴COOH → ¹⁴CO₂). We also tested the efficacy of the combined foam fractionation–EO treatment in natural waters by spiking ¹⁴C-PFOA and a cosolvent (CTAB) into PFAS-contaminated water obtained from two field sites with divergent PFAS concentrations and differing sources of PFAS contamination (natural drainage ditch vs. WWTP). Using a larger-scale tank (3500 mL), we observed that foam fractionation was 90% effective in removing ¹⁴C-PFOA from the WWTP effluent but only 50% effective for the drainage ditch water. Regardless, EO was highly effective in oxidizing ¹⁴C-PFOA in the foamate from both sources with half-lives (T_1/2) ranging from 8.7 to 15 min. While water chemistry differences between source waters may have influenced foam fractionation and require additional investigations, tank experiments provide the first proof-of-concept experiment using ¹⁴C-PFASs that foam fractionation and electrochemical oxidation can be used in tandem to treat PFAS-contaminated water. Full article

Iron phosphate (FePO₄·2H₂O) was synthesized via anodic oxidation using nickel–iron alloy composition simulates from laterite nickel ore as the anode and graphite electrodes as the cathode, with phosphoric acid serving as the electrolyte. A uniform experimental design was employed to systematically optimize the synthesis parameters including voltage, electrolyte concentration, electrolysis time, and degree of acidity or alkalinity (pH). The results indicate that the addition of cetyltrimethylammonium bromide (CTAB) surfactant effectively modulated the morphology of the anodic oxidation products. The optimized conditions were determined to be an electrolyte concentration of 1.2 mol/L, a voltage of 16 V, a pH of 1.6, an electrolysis time of 8 h, and a 3% CTAB addition. Under these conditions, the synthesized FePO₄·2H₂O exhibited enhanced performance as a lithium-ion battery precursor. Specifically, the corresponding LiFePO₄/C cathode delivered an initial discharge capacity of 157 mA h g⁻¹ at 0.2 C, retaining 99.36% capacity after 100 cycles. These findings provide valuable insights and theoretical foundations for the efficient preparation of iron phosphate precursors, highlighting the significant impact of optimized synthesis conditions on the electrochemical performance of lithium iron phosphate. Full article

CO₂-switchable surfactants, applicable for mitigating CO₂ geological storage efficiency challenges, offer promising control over foam stability under reservoir conditions, but their performance under extreme pressure, temperature, and salinity still needs thorough investigation. This study experimentally characterizes the performance of CO₂-switchable surfactants by evaluating their interfacial tension (IFT) reduction, foamability, and foam stability under reservoir-relevant conditions. Six surfactants, including cationic (cetyltrimethylammonium bromide (CTAB) and benzalkonium chloride (BZK)) and nonionic amine-based surfactants (N,N-Dimethyltetradecylamine, N,N-Dimethyldecylamine, and N,N-Dimethylhexylamine), were assessed using synthetic brine mimicking a depleted North Sea oil reservoir. A fractional factorial design was employed to minimize experimental runs while capturing key interactions between surfactant type, temperature, salinity, and divalent ion concentrations. Foam switchability was analyzed by alternating CO₂ and N₂ injections, and interfacial properties were measured to establish correlations between foam generation and IFT. Experimental findings demonstrate that cationic surfactants (BZK and CTAB) exhibit CO₂-switchability and moderate foam stability. Nonionic surfactants show tail length-dependent responsiveness, where D14 demonstrated the highest foamability due to its optimal hydrophilic–hydrophobic balance. IFT measurements revealed that BZK consistently maintained lower IFT values, facilitating stronger foam generation, while CTAB exhibited higher variability. The inverse correlation between IFT and foamability was observed. These insights contribute to the development of tailored surfactants for subsurface CO₂ storage applications, improving foam-based mobility control in CCS projects. Full article

Herein, a facile strategy was proposed to enhance the gas sensing performance of SnO₂ for H₂ by regulating its crystalline phase composition. Sn-based metal–organic framework (Sn-MOF) precursors with different morphologies were synthesized by introducing the surfactant cetyltrimethylammonium bromide (CTAB). Upon calcination, these precursors yielded either mixed-phase (orthorhombic and tetragonal, SnO₂-C) or single-phase (pure tetragonal, SnO₂-NC) SnO₂ nanoparticles. Structural characterization and gas sensing tests revealed that SnO₂-C exhibited a high response of 7.73 to 100 ppm H₂ at 280 °C, more than twice that of SnO₂-NC (3.75). Moreover, SnO₂-C demonstrated a faster response/recovery time (10/56 s), high selectivity, a ppb-level detection limit (~79 ppb), and excellent long-term stability. Notably, although the addition of CTAB reduced the specific surface area of SnO₂, the resulting lower surface area minimized oxygen exposure during calcination, facilitating the formation of a mixed-phase heterostructure. In addition, the calcination atmosphere of SnO₂-C (flowing air or Ar) was adjusted to further investigate the role of the crystal phase in gas sensing performance. The results clearly demonstrated that mixed-phase SnO₂ exhibited superior sensing performance, achieving a higher sensitivity and a faster response to H₂. These findings underscored the critical role of crystal phase engineering in the design of high-performance gas sensing materials. Full article

This work explores the role of cetyltrimethylammonium bromide (CTAB) as a morphology-directing agent in the hydrothermal synthesis of NiFe₂O₄ electrodes for high-performance supercapacitor applications. By fine-tuning CTAB concentrations (0.5%, 1%, and 1.5%), a tunable nanosheet morphology was achieved, with the NiFe-1 sample exhibiting uniformly interconnected nanosheets that enhanced ion diffusion, charge transport, and surface redox activity. Structural and surface analyses confirmed the formation of single-phase cubic NiFe₂O₄ and the presence of Ni²⁺ and Fe³⁺ oxidation states. Electrochemical characterization in a 2 M KOH electrolyte revealed that the NiFe-1 electrode achieved an areal capacitance of 8.21 F/cm² at 20 mA/cm², with an energy density of 0.34 mWh/cm² and a power density of 5.5 mW/cm². The electrode retained 79.61% of its capacitance after 10,000 cycles, demonstrating excellent stability. An asymmetric pouch-type supercapacitor device (APSD), assembled using NiFe-1 and activated carbon, exhibited an areal capacitance of 1.215 F/cm² and delivered an energy density of 0.285 mWh/cm² at a power density of 6.5 mW/cm² across a wide 0–1.8 V voltage window. These results confirm that CTAB-assisted nanostructuring significantly improves the electrochemical performance of NiFe₂O₄ electrodes, offering a scalable and effective approach for next-generation energy storage applications. Full article

Nanoparticles are proposed as alternatives to traditional antimicrobial agents. By manipulating a nanoparticle’s core and surface coating, antimicrobial effects against various microbial populations can be customized, known as the “designer effect”. However, the antimicrobial properties of nanoparticle core–coating combinations are understudied; little research exists on their effects on diverse bacteria. The antimicrobial effects of surface-stabilized zero-valent iron nanoparticles (FeNPs) are particularly interesting due to their stability in water and ferromagnetic properties. This study explores the impact of FeNPs coated with three surface coatings on six diverse bacterial species. The FeNPs were synthesized and capped with L-ascorbic acid (AA), cetyltrimethylammonium bromide (CTAB), or polyvinylpyrrolidone (PVP) using a bottom-up approach. Zone of inhibition (ZOI) values, assessed through the disc diffusion assay, indicated that AA-FeNPs and CTAB-FeNPs displayed the most potent antibacterial activity. Bacteria inhibition results ranked from most sensitive to least sensitive are the following: Bacillus nealsonii > Escherichia coli > Staphylococcus aureus > Delftia acidovorans > Chryseobacterium sp. > Sphingobacterium multivorum. Comparisons using ordinal regression and generalized linear mixed models revealed significant differences in bacterial responses to the different coatings and nanoparticle concentrations. The statistical model results are in agreement, thus increasing confidence in these conclusions. This study supports the feasibility of the “designer nanoparticle” concept and offers a framework for future research. Full article