Search Results (269)

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 work represents the first use of a phosphonium salt-functionalized β-Cyclodextrin polymer (β-CDP) as a highly selective sensing membrane for monitoring the safety of drinking water against perchlorate ions (ClO₄⁻) using electrochemical impedance spectroscopy (EIS). Structural confirmation via ¹H NMR, ¹³C NMR, ³¹P NMR, and FT-IR spectroscopies combined with AFM and contact angle measurements demonstrate how the enhanced solubility of modified cyclodextrin improves thin film quality. The innovation lies in the synergistic combination of two detection mechanisms: the “Host-Guest” inclusion in the cyclodextrin cavity and anionic exchange between the bromide ions of the phosphonium groups and perchlorate anions. Under optimized functionalization conditions, EIS reveals high sensitivity and selectivity, achieving a record-low detection limit (LOD) of ~10⁻¹² M and a wide linear range of detection (10⁻¹¹ M–10⁻⁴ M). Sensing mechanisms at the functionalized transducer interfaces are examined through numerical fitting of Cole-Cole impedance spectra via a single relaxation equivalent circuit. Real water sample analysis confirms the sensor’s practical applicability, with recoveries between 96.9% and 109.8% and RSDs of 2.4–4.8%. Finally, a comparative study with reported membrane sensors shows that β-CDP offers superior performance, wider range, higher sensitivity, lower LOD, and simpler synthesis. Full article

In this study, natural kaolin was modified with hexadecyltrimethylammonium bromide (HDTMA-Br) at two levels corresponding to 50% and 90% of its cation exchange capacity. The resulting materials, designated as HKR-50 and HKR-90, were used as adsorbents for the mycotoxins ochratoxin A (OCHRA) and zearalenone (ZEN). The characterization of the HKRs with several methods (X-ray diffraction, DRIFT spectroscopy, thermal analysis (DTA/TG), SEM, zeta potential measurements, and the determination of the point of zero charge and textural properties) confirmed the presence of surfactant ions on the organokaolinites’ surfaces. The adsorption of ZEN and OCHRA by HKRs followed nonlinear adsorption isotherms, suggesting a complex adsorption mechanism. The adsorption capacities of ZEN and OCHRA were similar for HKR-50 and HKR-90 at pH 3, with higher adsorption observed for ZEN (~13.0 mg/g for HKR-50 and HKR-90 for ZEN and ~8.0 mg/g for HKR-50 and HKR-90 for OCHRA). At pH 7, the adsorption of ZEN and OCHRA was lower than at pH 3, especially for OCHRA, but slightly increased with increased amounts of surfactant on the kaolinite surface (8.5 mg/g for HKR-50 and 10.8 mg/g for HKR-90 for ZEN and 2.6 mg/g for HKR-50 and 4.1 mg/g for HKR-90 for OCHRA). Special attention was paid to the safety assessment of the natural kaolin and HKR-90, and toxicological tests confirmed the safety of both materials, as no adverse effects were observed in rats. 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

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

This study examined a proposed system integrating waste power plants, a utility grid, and battery technologies to optimize energy operations for the On-nut community in Bangkok. The system was modeled through experimental, mathematical, and schematic approaches to identify the most efficient energy generation and cost management strategies utilizing lithium, flow, and zinc bromide batteries. This was achieved by employing industrial smart grid analysis, closed-loop algorithms, and feedback control systems to manage energy flow econometrics through switching operations, thereby maximizing electric cost efficiency and network service from the integrated system architectures (grid/lithium/biogas, grid/flow/biogas, and grid/zinc bromide/biogas systems). The proposed configuration of the biogas generator/grid/lithium-ion storage network demonstrated the highest technical efficiency in energy purchases, totaling 239,764 kWh, with energy sales to the grid amounting to 1,959,426 kWh and the lowest net energy purchase from the grid at 1,719,661 kWh. Conversely, the biogas generator/grid/zinc bromide storage configuration achieved the most economical network, reflected in an overall current cost of USD 8,647,863.00, an operating cost of USD 143,974.00, an investment return rate of 17.00%, an internal return rate of 20.30%, and a payback period of 4.83 years. The biogas generator/grid/zinc bromide network exhibited the highest performance ratio at 80.55%, surpassing the flow battery at 79.65% and lithium-ion at 78.89% in terms of energetic configurations. Full article

This work describes the synthesis, crystal structure, and hydrophobicity tests of four bismuth(III)– and silver(I)–bromide complexes using the triammonium cations diethylenetriaminonium (H₃DETA³⁺) and N,N,N′,N″,N‴-pentamethyldiethylenetriammonium (H₃PMDTA³⁺). The prepared compounds are the 0D perovskites (H₃DETA)[BiBr₆] (1), (H₃DETA)₂[AgBr₄]Br₃ (2), and (H₃PMDTA)[BiBr₆] (3), as well as the 1D/2D mixed perovskite with minimum formula (H₃PMDTA)[Ag₃Br₆] (4), being the last three novel materials. Compounds 1 and 3 crystallize in the orthorhombic P2₁2₁2₁ space group and are discrete [BiBr₆]³⁻ units with the cation surrounding them. In both compounds, the bismuth(III) metal ion is found in a distorted octahedral coordination geometry. Compound 2 crystallizes in the monoclinic P2₁/c space group, and it is a mixed salt consisting of (H₃DETA)[AgBr₄] and (H₃DETA)Br₃, whereas the silver(I) complexes are also isolated. Finally, compound 4, which crystallizes in the orthorhombic space group Pbcn, is a combination of a 2D and 1D silver–bromide perovskite, with the cations filling the voids. The 2D structure has the minimal formula [Ag₄Br₇]³⁻, with the 1D coordination polymer [Ag₂Br₅]³⁻ being both built up by a combination of bromide ions acting as tetrahedra corner and edge-sharing bridging ligands. The silver(I) in 2 and 4 is found in a tetrahedral coordination geometry. All compounds were deposited on pristine FTO glass, resulting in an increase in the contact angle from 22° to 44°, 36°, 62°, and 54° for films of 1, 2, 3, and 4, respectively. Compounds 1 and 3 were also deposited onto Cs₂AgBiBr₆ film, and the contact angles were observed to be the same as when deposited directly onto the FTO cover glass. Full article

Groundwater is a critical resource in semi-arid regions like Morocco’s Guire Basin, yet pollution and overexploitation threaten its sustainability. This study evaluates the groundwater quality of the Guire aquifer (Eastern High Atlas) using an integrated approach combining hydrochemical, isotopic (δ¹⁸O, δ²H, δ¹³C), multivariate statistical, and Geographic Information System (GIS) analyses alongside the Water Quality Index (WQI). Sixteen wells were monitored for physicochemical parameters (pH: 7–7.9; EC: 480–3004 μS/cm; BOD5: 1.03–30.5 mg/L; COD: 10.2–45.75 mg/L) and major ions, revealing widespread exceedances of Moroccan standards for Cl⁻, HCO₃⁻, Mg²⁺, Ca²⁺, and NH₄⁺. WQI classified 81% of samples as “Poor” to “Unsuitable for drinking” (WQI: 51–537), driven by elevated Cl⁻, Na⁺, and SO₄²⁻ from Triassic evaporite dissolution and NO₃⁻ (up to 45 mg/L) from agricultural runoff. Stable isotopes (δ¹⁸O: −7.73‰ to −5.08‰; δ²H: −66.14‰ to −44.20‰) indicate Atlantic-influenced recharge at 900–2200 m altitudes, with a δ¹⁸O-δ²H slope of 5.93 reflecting evaporation during infiltration. Strontium (Sr²⁺/Ca²⁺: 0.0024–0.0236) and bromide (Br/Cl: 8.47 × 10⁻⁵–9.88 × 10⁻⁴) ratios further confirm evaporitic dominance over anthropogenic contamination. This work provides actionable insights for policymakers, advocating for targeted restrictions on fertilizers, enhanced monitoring near evaporite zones, and artificial recharge initiatives. By linking geogenic/anthropogenic contamination to governance strategies, this study advances sustainable groundwater management in semi-arid regions. 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

This study extends previous machine learning work on ion constituent simulation in California’s Sacramento–San Joaquin Delta (Delta) to include three critical water intake locations. The developed Artificial Neural Network models demonstrate exceptional accuracy (R² > 0.96) in predicting chloride, bromide, and sulfate concentrations at these strategically important facilities. Water intake location models show substantial improvements in prediction accuracy, with MAE reductions of 60.7–74.0% for chloride, 63.3–72.5% for bromide, and 70.4–87.9% for sulfate, compared to existing methods for the Interior Delta. Performance evaluation through comprehensive cross-validation confirms robust model stability across varied conditions, with remarkably consistent metrics (standard deviation in R² ≤ 0.006). Four complementary interactive dashboards were developed, enabling users, regardless of programming expertise, to simulate ion constituents throughout the Delta system. A Model Interpretability Dashboard specifically addresses the complexity of machine learning models by visualizing parameter sensitivity and prediction behavior, thereby enhancing transparency and building stakeholder trust in the modeling approach. For the first time, spatial coverage limitations are addressed through hybrid modeling that combines DSM2 hydrodynamic simulation with machine learning to enable continuous prediction of ion distributions across several points in the Interior Delta. These advancements provide water managers with accessible, accurate tools for informed decision-making regarding agricultural operations, drinking water treatment, and ecosystem management in this vital water resource. Full article

IR-780 is a heptamethine cyanine dye that exhibits strong absorbance in the near-infrared region. Herein, we report IR-780 dye as a dual sensor for chromogenic cyanide detection and azide’s fluorogenic sensing in acetonitrile. Cyanide and hydroxide cause instant, dramatic color changes in the dye solution from green to yellow and dramatic spectral changes in the UV-Vis spectrum. The interaction of cyanide and hydroxide with the dye caused a dramatic decrease in the intensity of the strong absorption band at 780 nm and a concomitant band appearance at 435 nm. Other monovalent ions, including fluoride, chloride, bromide, iodide, dihydrogen phosphate, thiocyanate, acetate, and dihydrogen arsenate, caused no significant color or spectral changes. UV-Vis studies showed that the IR-780 dye is sensitive and selective to both ions. The detection limits for cyanide and azide are 0.39 µM and 0.50 µM, respectively. Interestingly, the IR-780 dye exhibited strong fluorescence at 535nm upon interaction with azide, while its initial emission at 809 nm was quenched. Both UV-Vis and fluorescence spectroscopy accomplished the detection of cyanide and azide using IR-780. Furthermore, the sensor’s effectiveness in fluorescence imaging of intracellular CN⁻ ions is demonstrated in live HeLa cells. 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

In this article, Pt-Sn_xO_y hybrid nanoparticles encaged in porous silica nanospheres (Pt-Sn_xO_y@PSNs) were prepared by using 1-dodecanethiol (C₁₂-SH) as a coordination agent to confine Pt and Sn ions in a microemulsion system, which is formed by cetyltrimethylammonium bromide (CTAB) and C₁₂-SH as co-surfactants in water. Compared with Pt@PSNs, when different molar ratios of Sn_xO_y were introduced into Pt@PSNs to form Pt-Sn_xO_y@PSNs, the catalytic efficiency of 4-nitrophenol (4-NP) reduction with NaBH₄ can be significantly enhanced. At molar ratios of 4-NP/Pt of 150/1, the 4-NP conversion reached 100% over Pt-Sn_xO_y@PSNs with Pt/Sn molar ratios of 1/0.75 in 8 min. This catalytic performance showed a slight decrease after six reaction cycles. This enhanced catalytic efficiency can be ascribed to the synergistic effect between Pt and Sn_xO_y, and the protection of porous silica nanostructures can effectively improve the stability of the catalyst. Full article

Humidity sensors are widely utilized in meteorological research, industrial production, precision instrument maintenance, agriculture, health care, and other fields. However, the long response time and low sensitivity of current metal oxide and hybrid humidity sensors limit their practical applications. In this study, a humidity sensor was prepared using a simple drop-casting method with 2-hydroxy-2-methylpropiophenone (HOMPP) and 1-vinyl-3-butylimidazolium bromide (C₉H₁₅BrN₂) as the humidity sensing materials. This approach offers advantages such as low cost, high chemisorption capacity, and excellent moisture-sensitive performance. The prepared humidity sensors demonstrate high sensitivity, good repeatability, excellent flexibility, low hysteresis, and response/recovery times of 6/12.5 s, respectively, over a wide relative humidity (RH) range (2–97%). Additionally, the sensor exhibits potential for various multifunctional applications, including humidity detection in daily life, respiratory monitoring, non-contact sensing, and flexible electronics applications. Full article