Water Solution Research Articles

New Insights into ZIF-90 Synthesis

Zeolitic imidazolate frameworks (ZIFs) are traditionally synthesized using N, N-dimethylformamide (DMF). However, DMF is toxic and hazardous to human health and the environment, hence other alternative solvents need to be considered. Herein, three different solvents like methanol, water and acetone were used to replace DMF and to explore the syntheses of ZIF-90 using a conventional and a microwave-assisted solvothermal method to obtain hydrothermally stable products, which also exhibit an increased water uptake. Pure ZIF-90 was synthesized under ambient pressure at 60 °C for 90 min using the conventional solvothermal method in an acetone–water solution, while under microwave irradiation it was formed in only 5 min at 80 °C. Altering methanol, water and acetone in the reaction mixture significantly affected the structural and water adsorption properties of ZIF-90s, which were monitored via PXRD, TGA, nitrogen and water sorption, and SEM. The highly efficient, less toxic, low-cost and activation-free microwave synthesis resulted in the formation of ZIF-90 nanoparticles that exhibited the highest maximum water adsorption capacity (0.37 g/g) and the best hydrothermal stability between water adsorption at 30 °C and desorption at 100 °C at 12.5 mbar among all the products obtained.

The effect of carbon coating on the arsenite sorption by magnetic carbon nanocomposites

AbstractArsenic pollution has emerged through anthropogenic activities and natural mineral leaching processes. This study aims to advance the use of magnetic carbon nanocomposites (MCNs) in the sorption of arsenic, studying the influence of feedstock and the presence of carbon coating on magnetic nanoparticles. Previous works have shown that post-pyrolysis treatment improves the stability of MCNs by reducing iron leaching due to the formation of a carbon coating that encapsulates the iron oxide nanoparticles. However, this carbon coating could influence the adsorption properties of MCNs. This investigation deals with arsenic adsorption by four MCNs prepared by co-precipitation of magnetite (Fe3O4) nanoparticle into four carbonaceous matrixes, followed by a post-pyrolysis treatment. The pristine carbonaceous matrixes used in the present work were commercial activated carbon (CAC), charcoal (CC), hydrochar from the orange residue (HCOR), and biochar from sunflower husk (BCSFH). Pristine carbonaceous materials and MCNs without post-pyrolyzed were also used as arsenic sorbents in water solutions. Additionally, kinetic studies were carried out to explore the sorption properties of different MCNs and pristine materials, concerning the removal efficiencies (expressed as a percentage) and adsorption capacities, determining the equilibrium time. The results demonstrated that the presence of magnetite increases the adsorption of arsenic, being higher in the case of materials obtained by direct co-precipitation than in materials subjected to a post-pyrolysis process. The presence of a carbon layerprotecting the magnetite slightly decreases the adsorption of arsenic.

Ac/dc conductivity and ML-based evaluation of electric characteristics of methylene blue solution

Utilizing a precision LCR meter, the complex permittivity ε*(f) of methylene blue (MB) solutions in distilled water (DW) was determined at various temperatures and concentrations in the lower frequency range from 20 Hz to 2 MHz. The complex ac conductivity σ*(f) of the liquid samples was calculated using ε*(f). DC conductivity, σdc of the samples was also calculated. The effect of changes in temperature and concentration on the σ*(f) and ε*(f) of solutions are examined. A solution of MB in DW, ranging from diluted to concentrated, greatly enhances the electrical conductivity σdc. The empirical Casteel-Amis (CA) formula was employed to fit the experimental σdc values at different concentrations. Accurate measurement of complex permittivity of liquid solutions over wide range of concentration at broad range of frequencies and temperature is laborious and uneconomical. Therefore, we performed the complex permittivity measurement of the aqueous solution of MB over a limited concentration and temperature range over 201 frequency point. Then we used this experimental data in CatBoost regression model to predict the dielectric properties at intermediate frequencies and various concentrations. This model was employed to assess the performance of material characteristics using R-squared score. The study demonstrated that the CatBoost regression model can predict material performance at intermediate frequencies and concentrations while decreasing measurement resource needs by 60 %.

Removal of crocein orange G from water solutions by trimetallic nanoparticles [Co/Cu/M (M=Ni, Zn)] prepared by chemical reduction method

Co-Cu-Ni and Co-Cu-Zn trimetallic nanoparticles (NPs) were prepared by chemical reduction method which were then used as adsorbent to remove Crocein Orange G dye from solution. The elemental composition of the fabricated NPs was determined by EDX analysis, surface morphology was assessed by SEM, and its crystalline nature was confirmed by XRD analysis. The functional groups on nanoparticles were confirmed by FT-IR analysis. The optimum dosage was found to be 0.01 g. Langmuir model as well as linear pseudo 2nd order kinetics models best explained the obtained data. The maximum adsorption capabilities were found to be around 497.618 mg/g and 683.093 mg/g, respectively for Co-Cu-Ni and Co-Cu-Zn trimetallic NPs. The adsorption process was exothermic, as evidenced from the positive ΔH° values. The negative values of ΔG° at the corresponding temperatures support the spontaneous nature of the adsorption processes. The positive entropy changes (ΔS°) suggested that there is more disorderness at the interface between the solid and the solution during the adsorption. The fabricated trimetallic nanoparticles have effectively adsorbed Crocein Orange G, which may be considered as an attractive option in wastewater treatment and environmental remediation applications due to diversity of metal ions on surface offering differential attractive forces for pollutant.

A Coordinating Small Organic Molecule with Tunable Lower Critical Solution Temperature for Efficient Management of Solar Radiation.

Structurally well-defined small molecules with lower critical solution temperature (LCST) behavior offer enormous prospects for fine-tuning their phase transition properties to be "on-demand" applied in the specific scene but are still underexplored. Herein, a novel amphiphilic small LCST molecule is rationally designed and synthesized. The molecule, namely TG, features a conjugation of multiple short ethylene glycol (EG) chains with the functional coordinating terpyridine (Tpy) moiety. The molecule TG demonstrates excellent LCST behavior down to 0.05× 10-3 m in a water solution. And a cloud point Tcp = 30.9°C with a very short thermal hysteresis ΔT = 0.2°C and good reversibility can be achieved when c = 0.1× 10-3 m. The excellent LCST properties of TG have enabled its successful performance as the smart window for solar radiation management with the ∆Tlum, ∆TIR, and ∆Tsol being 83.6%, 49.1%, and 67.2%, respectively. Moreover, the presence of Tpy moiety in TG enables its coordination with Ru3+ and the resulting complex also exhibits modulated LCST behavior with different concentration-dependent Tcp. These studies would provide novel small-molecule-based scaffolds for constructing better solar radiation management systems as well as other thermal-responsive smart materials.

A laser-induced superhydrophobic surface with multiple microstructures for stable drag reduction

To address the issue of water resistance in ship navigation, we developed a drag-reducing surface based on the microstructure of shark skin and a superhydrophobic coating. First, grooves with various microstructures were fabricated on the substrate surface using laser processing. Then, a mixture of octadecyltrichlorosilane, water, and silica solution was uniformly sprayed onto the grooved substrate surface to achieve superhydrophobicity. To enhance and stabilize the drag reduction effect, we optimized the width and spacing of the grooves by adjusting the laser processing parameters, achieving a high drag reduction rate under various flow conditions. In the Reynolds number range of 2 × 105 to 5 × 105, the drag reduction rate of the superhydrophobic coated surface with grooves reached over 66.57 %, which is an improvement of 7 % to 26.51 % compared to the superhydrophobic coated surface without grooves. Additionally, the oxides accumulated on the ribs after laser ablation can slow down the wear of the superhydrophobic coating, significantly enhancing the surface's mechanical durability. This simple and cost-effective surface provides a new approach for laser preparation of drag-reducing surfaces.

Development of a fast and low-cost aqueous based-extraction protocol for the simultaneous extraction and characterization of SiO2 and TiO2 (nano)particles in confectionary products.

BackgroundThe determination of (nano)particulate content from food additives has been a long-standing concern for authorities since it is of vital importance for ensuring food safety, regulatory adherence, and transparent consumer information. Nonetheless, a critical step in these determinations is the refinement of a careful and quantitative extraction process for particles that may be found within complex matrices such as confectionery products. The development of new technologies and analysis methods for nanoparticles is ongoing. Whereas new technologies and analysis methods for nanoparticles are being developed, the extraction of (nano)particles of different nature has not been adequately addressed in the literature. ResultsA simple aqueous extraction procedure was found to be suitable for the simultaneous extraction of TiO2 and SiO2 (nano)particles from five confectionery products. Neither the extraction agents (water, lipase, pancreatin and Tris-HCl solutions) nor the methods (manual shaking, ultrasonic bath, ultrasonic probe and ultrafiltration) altered the size, morphology, or aggregation state of either type of particle, as revealed by the micrographs obtained by Transmission Electron Microscopy (TEM). Single-particle ICP-MS (spICP-MS) determined that the optimal conditions for extracting both types of particles involve manual shaking using water as the solvent. Furthermore, the use of enzymes seemed to hinder the determination of both types of particles by spICP-MS. (Nano)particles of TiO2 and SiO2 were detected in all the confectionaries, even though the E171 additive was only labelled in one of them. The average percentage of nanoparticulate TiO2 material in the evaluated products was 30 %, while no nanometer-sized particles of SiO2 were detected. SignificanceEnsuring food safety, regulatory compliance and transparent consumer information relies on getting reliable results that connect with the application of sample treatment procedures for detecting unaltered nanoparticles in food products. The presented research introduces an economical, swift, user-friendly, environmentally responsible, and harmonious extraction method for the concurrent analysis of TiO2 and SiO2 particles in confectionery samples. Furthermore, particles from additives not included in the labeling have been detected, characterized, and quantified in the confectionary products.

No signs of microbial-influenced corrosion of cast iron and copper in bentonite microcosms after 400 days

High-level radioactive waste needs to be safely stored for a long time in a deep geological repository by using a multi-barrier system. In this system, suitable barrier materials are selected that ideally show long-term stability to prevent early radionuclide release into the biosphere. In this study, different container matals (copper and cast iron) and pore water compositions (Opalinus Clay pore water and saline cap rock solution) were combined with Bavarian bentonite in static batch experiments to investigate microbial-influenced corrosion. The increasing concentration of iron and copper in the solution as well as detected corrosion products on the metal surface are indicative of anaerobic corrosion of the respective metals during an incubation of 400 days at 37°C. However, although the intrinsic microbial bentonite community was stimulated with either lactate or H2, an acceleration of cast iron- and copper corrosion did not occur. Furthermore, neither corrosive bacteria nor conventional bacterial corrosion products, such as metal sulfides, were detected in any of the analyzed samples. The analyses of geochemical parameters (e.g. ferrous iron-, iron-, copper- and potassium concentrations as well as redox potentials) showed significant changes in some cast iron- and copper-containing setups, but these changes did not correlate with the microbial community structure in the respective microcosms, as confirmed by statistical analyses. Hence, the analyzed Bavarian bentonite (type B25) showed no significant contribution to cast iron and copper corrosion under the applied conditions after 400 days of incubation. From this perspective, bentonite B25 could be a suitable candidate as a geotechnical barrier in future repositories.

Silicon phthalocyanines functionalized withaxial substituents targeting PSMA: synthesisand preliminary assessment of their potential for PhotoDynamic Therapy of prostate cancer.

Photodynamic therapy (PDT) is a clinical modality based on the irradiation of different diseases, mostly tumours, with light following the selective uptake of a photosensitiser by the pathological tissue. In this study, two new silicon(IV)phtalocyanines (SiPcs) functionalized at both axial positions with a PSMA inhibitors are reported as candidate photosensitizers for PDT of prostate cancer, namely compounds SiPc-PQ(PSMAi)2 and SiPc-OSi(PSMAi)2. These compounds share the same PSMA-binding motif, but differ in the linker that connects the inhibitor moiety to the Si(IV) atom: an alkoxy (Si-O-C) bond for SiPc-PQ(PSMAi)2, and a silyloxy (Si-O-Si) bond for SiPc-OSi(PSMAi)2. Both compounds were synthesized by a facile synthetic route and fully characterized by 2D NMR, mass spectrometry and absorption/fluorescence spectrophotometry. The PDT agents showed a suitable solubility in water, where they essentially exist in monomeric form. SiPc-PQ(PSMAi)2 showed a higher singlet oxygen quantum yield ΦΔ, higher fluorescence quantum yields ФF and better photostability than SiPc-OSi(PSMAi)2. Both compounds were efficiently taken up by PSMA(+) PC3-PIP cells, but not by PSMA(-) PC3-FLU cells. However, SiPc-PQ(PSMAi)2 showed a more specific photoinduced cytotoxicity in vitro, which is likely attributable to a better stability of its water solutions.

Comprehensive Performance Analysis of Hybrid Solar Water Heating Systems: Synergizing Photovoltaic and Thermal Technologies

Abstract: Solar water heaters are an efficient and sustainable technology for meeting the growing demand for hot water in residential and commercial applications. This abstract presents a comprehensive overview of the performance evaluation of solar water heater systems through an extensive experimental study. The study aims to assess the effectiveness and efficiency of different solar water heater configurations under varying operating conditions. The experimental investigation involved the measurement and analysis of key performance parameters such as solar collector efficiency, heat transfer efficiency, thermal storage capacity, and overall system efficiency. A range of factors including solar radiation intensity, ambient temperature, water flow rate, and collector tilt angle were systematically varied to examine their impact on system performance. The results of the experimental study demonstrated the significant potential of solar water heaters in providing cost-effective and environmentally friendly hot water solutions. The solar collector efficiency was found to be highly influenced by the solar radiation intensity, with higher levels of solar irradiation leading to increased thermal energy generation. The heat transfer efficiency was optimized by adjusting the water flow rate and collector tilt angle, ensuring efficient transfer of heat from the collector to the water. Furthermore, the thermal storage capacity of the system played a crucial role in maintaining a consistent supply of hot water during periods of low solar radiation or high demand. Overall system efficiency was found to be strongly dependent on the integration of efficient heat exchangers and insulation materials. Based on the experimental findings, recommendations for system design and optimization were formulated, highlighting the importance of proper sizing, selection of suitable materials, and appropriate control strategies. The results also identified areas for future research, such as the integration of advanced heat transfer enhancement techniques and the utilization of hybrid solar water heater systems

Comprehensive Performance Analysis of Hybrid Solar Water Heating Systems: Synergizing Photovoltaic and Thermal Technologies

Abstract: Solar water heaters are an efficient and sustainable technology for meeting the growing demand for hot water in residential and commercial applications. This abstract presents a comprehensive overview of the performance evaluation of solar water heater systems through an extensive experimental study. The study aims to assess the effectiveness and efficiency of different solar water heater configurations under varying operating conditions. The experimental investigation involved the measurement and analysis of key performance parameters such as solar collector efficiency, heat transfer efficiency, thermal storage capacity, and overall system efficiency. A range of factors including solar radiation intensity, ambient temperature, water flow rate, and collector tilt angle were systematically varied to examine their impact on system performance. The results of the experimental study demonstrated the significant potential of solar water heaters in providing cost-effective and environmentally friendly hot water solutions. The solar collector efficiency was found to be highly influenced by the solar radiation intensity, with higher levels of solar irradiation leading to increased thermal energy generation. The heat transfer efficiency was optimized by adjusting the water flow rate and collector tilt angle, ensuring efficient transfer of heat from the collector to the water. Furthermore, the thermal storage capacity of the system played a crucial role in maintaining a consistent supply of hot water during periods of low solar radiation or high demand. Overall system efficiency was found to be strongly dependent on the integration of efficient heat exchangers and insulation materials. Based on the experimental findings, recommendations for system design and optimization were formulated, highlighting the importance of proper sizing, selection of suitable materials, and appropriate control strategies. The results also identified areas for future research, such as the integration of advanced heat transfer enhancement techniques and the utilization of hybrid solar water heater systems

Comparative Evaluation of Antifungal Efficacy of 3% Sodium Hypochlorite, 2% Chlorhexidine Gluconate, Ozonated Water, Alum Water, and Normal Saline Solutions against Endodontopathogenic Microorganism, Candida Albicans: A Microbiological In Vitro Study

Comparative Evaluation of Antifungal Efficacy of 3% Sodium Hypochlorite, 2% Chlorhexidine Gluconate, Ozonated Water, Alum Water, and Normal Saline Solutions against Endodontopathogenic Microorganism, Candida Albicans: A Microbiological In Vitro Study

Early-age hydration of tricalcium aluminate in chloride solutions

Understanding the kinetics and mechanisms involved in early-age hydration of tricalcium aluminate (C3A) in chloride solutions holds promise for implementing seawater-mixed concrete in the marine environment, as C3A remains the most reactive component of Portland cement (PC), affecting both PC and concrete's early-age hardening and long-term durability. Herein, we conducted a series of meticulously designed ex-situ and in-situ experiments to elucidate the intricate hydration behaviors of C3A in various chloride solutions. The results reveal that C3A exhibits distinct hydration kinetics and structural evolution processes in different solutions. The rapid precipitation of alumino-ferrite-mono (AFm) and C3AH6 phases contributes to the swift development of hydration heat and storage modulus in water and NaCl solutions, with a slight acceleration observed in the later one. Conversely, the formation of C3AH6 is delayed in CaCl2 and MgCl2 solutions before 20 min, with the subsequent precipitation of Cl-AFm enhancing its later production, particularly in CaCl2 solutions. Ab-initio calculations further elucidate that the acceleration effect of Cl ions originates from the ionization and structurization of hydrated surface Ca ions. However, this positive effect is significantly offset by Cl pairing with counterions, resulting in a dramatic adverse effect of solution Ca ions originated from the negative entropy effect of structuralized water molecules and electrostatic repulsion with like-charged surface Ca ions and solvent dipoles. Our findings provide valuable insights for sustainable and durable designs on cement-based materials mixed with seawater.

Characterization of human Aquaporin ion channels in a yeast expression system as a tool for novel ion channel discovery.

Aquaporin (AQP) channels found in all domains of life are transmembrane proteins which mediate passive transport of water, glycerol, signaling molecules, metabolites and charged solutes. Discovery of new classes of ion-conducting AQP channels has been slow, likely reflecting time- and labor-intensive methods required for traditional electrophysiology. Work here defines a sensitive mass-throughput system for detecting AQP ion channels, identified by rescue of cell growth in the K+-transport-defective yeast strain CY162 following genetic complementation with heterologously expressed cation-permeable channels, using the well characterized human AQP1 channel for proof of concept. Results showed AQP1 conferred transmembrane permeability to cations which rescued survival in CY162 yeast. Comprehensive testing showed that growth response properties fully recapitulated AQP1 pharmacological agonist and antagonist profiles for activation, inhibition, dose-dependence, and structure-function relationships, demonstrating validity of the yeast screening tool for AQP channel identification and drug discovery efforts. This method also provided new information on divalent cation blockers of AQP1, pH sensitivity of antagonists, and ion permeability of human AQP6. Site-directed mutagenesis of AQP1 channel regulatory domains confirmed that yeast growth rescue was mediated by the introduced channels. Optical monitoring with a lithium-sensitive photoswitchable probe in living cells independently demonstrated monovalent cation permeability of AQP1 channels in yeast plasma membrane. Ion channel properties of AQP1 expressed in yeast were consistent with those of AQP1 expressed in Xenopus laevis oocyte and K+-transport defective Escherichia coli. Outcomes here establish a powerful new approach for efficient screening of phylogenetically diverse AQPs for yet untested functions as cation channels.

Early-stage recovery of lithium from spent batteries via CO2-assisted leaching optimized by response surface methodology

Recycling lithium (Li) from spent lithium-ion batteries (LIBs) due to the depletion of natural resources and potential toxicity is becoming a progressively favourable measure to realize green sustainability. Presently, the prevalent recycling technique relying on pyrometallurgy lacks the capability to extract lithium. Meanwhile, conventional hydrometallurgical processes frequently employ robust acidic solutions like sulfuric acid and precipitation agents such as sodium carbonate. Unfortunately, this approach tends to result in the extraction of lithium at the end of a lengthy process chain, leading to associated losses and creating challenges in managing complex waste. This study addresses a cost-effective and environmentally friendly early-stage lithium recovery from the thermally conditioned black mass. In this sense, a thermally conditioned black mass is subjected to the carbonization process in a water solution to transform the water-insoluble Li phase into soluble lithium bicarbonate (LiHCO3) and carbonate (Li2CO3) facilitating its selective separation from other elements. Response surface methodology (RSM)—a statistical tool integrated with central composite design (CCD) is employed to optimize the parameters for Li recovery. Temperature, solid–liquid (S/L) ratio, leaching time and CO2 flow rate are considered as variable factors in modelling the optimum recycling process. A quadratic regression model is developed for Li recovery and based on ANOVA analysis, (S/L) ratio, temperature and time are identified as statistically significant factors. Experimental results demonstrate a maximum leaching efficiency of lithium with optimized parameter set, achieving a recovery rate of 97.18% with a fit response of 93.54%.

Steady State and Time-Resolved Fluorescence Spectroscopy of Cinchonine Dication in Sodium Dodecylsulphate Micellar System.

This paper reports the influence of surface charge of the micelles on to the photophysical properties of a cinchonine dication (C2+) fluorophore in anionic, sodium dodecylsulphate (SDS), surfactant at premicellar, micellar and post-micellar concentrations in aqueous phase at room temperature. The magnitude of edge excitation red shift (EERS) in the fluorescence maximum of C2+ in bulk water solution is 1897cm- 1 whereas, in the case of SDS it is observed to be 1984cm- 1. The fluorescence decay curve of C2+ fits with multi exponential functions in the micellar system. The increase in lifetime of C2+ in SDS has been attributed to the increase in radiative rate due to the incorporation of C2+ at the micelle -water interface. The value of dynamic quenching constant determined is 16.9 M- 1. The location of the probe molecule in micellar systems has been justified by a variety of spectral parameters such as dielectric constant, ET (30), viscosity, EERS, average fluorescence decay time, radiative and non-radiative rate constants. All experimental results suggest that the C2+ molecule binds strongly with the SDS micelles and resides at micellar-water interface. The binding constant (Kb) calculated (3.85 × 105 M- 1) for C2+ in SDS revealed that the electrostatic forces mediate charge probe-micelle association.

Equilibrium vapor pressure of aqueous sodium acetate and potassium acetate solutions used as working fluids in frost-free air–source heat pumps at 263–328 K

Aqueous solutions of sodium acetate (CH3COONa) and potassium acetate (CH3COOK) are considered effective alternative heat exchange media for frost-free air–source heat pumps (FFASHPs) owing to the low corrosiveness, low viscosity, and low cost. Equilibrium vapor pressure is the most crucial property that characterizes freezing point and latent heat transfer. However, studies on this property, especially in subzero temperature ranges are scarce. This study was conducted to experimentally investigate the equilibrium vapor pressure of CH3COONa and CH3COOK solutions. The developed apparatus and procedures were based on the static method, and validated by evaluating the vapor pressure of distilled water, n-heptane, and calcium chloride (CaCl2) aqueous solution. Their average absolute deviations were within 1.94%. As the temperature increased from 263 to 328 K and solute concentration increased from 9.27 to 33.81 wt%, 124 data points of the vapor pressure of the CH3COONa and CH3COOK solutions were obtained, ranging from 0.2759 to 13.2608 kPa. Modified Antoine equation and ion interaction (Pitzer) model were established for correlation of the experimental data. The average absolute deviations of the CH3COONa and CH3COOK solutions produced by Antoine equation were 2.08 and 2.48%, respectively. Those produced by Pitzer model further decreased to 1.36 and 1.45% due to the import of osmotic coefficient and the accuracy improvement. Furthermore, according to the experimental and calculation results, the vapor pressure of the CH3COONa solution was lower than that of the CH3COOK solution. Therefore, under the same antifreezing conditions, the CH3COONa solution facilitates latent heat absorption from ambient air, while the CH3COOK solution is conducive to achieve regeneration. The results of this study provide foundational data for the vapor pressure of the two solutions and can promote their application in FFASHPs.

Effect of KOH- and NaOH-modified fly ash on the adsorption of methylene blue and crystal violet dyes: a Box-Behnken design study

ABSTRACT Coal Fly Ash (FA) and modified fly ash (mFA), treated with either KOH or NaOH, were used to remove methylene blue (MB) and crystal violet (CV) dyes from aqueous solution. Several techniques, including Thermogravimetric analysis, X-Ray diffraction analysis, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller, and Scanning Electron Microscopy, were used to characterise both FA and mFA. To optimise the adsorption process, the Response Surface Methodology (RSM) with the Box – Behnken design (BBD) was applied. Key parameters such as solution pH (4–10), initial dye concentration (200–300 mg/L), contact time (15–180 minutes), and temperature (30–50°C) were varied to assess their impact on adsorption efficiency. The adsorption followed the Langmuir model and pseudo-second-order (PSO) kinetic model. The adsorption capacity of mFA for MB dye was 49.5 mg/g at 50°C, while for CV dye, it was 495.5 mg/g at the same temperature. The adsorption mechanism involved electrostatic attraction, n-π interaction, Yoshida hydrogen bonding, and hydrogen bonding. These results highlight the effectiveness of mFA as a high-capacity adsorbent for treating MB and CV dyes in water solutions.

A novel approach to integrate CCHP systems with desalination for sustainable energy and water solutions in educational buildings

ABSTRACT This study presents a novel approach to integrating combined cooling, heating, and power (CCHP) systems with water desalination for enhanced energy and water management in educational buildings. Two distinct layouts for CCHP and desalination systems are introduced: one prioritizing efficient power generation to meet electricity demands while providing waste heat for desalination, and the other focusing on balancing cooling and heating loads alongside water desalination. Both layouts are tailored to meet the building's energy and water demands while considering operational efficiency. Optimization of these layouts against traditional systems using the bat search algorithm emphasizes economic viability and the gas engine's operational flexibility, which are crucial for partial load operation. In addition, an environmental assessment compares the proposed CCHP-desalination systems with conventional setups, assessing CO2 emission reductions and overall sustainability. The evaluation encompasses key environmental metrics, such as resource consumption and the integration of renewable energy sources. Results highlight significant CO2 emission reductions across various gas engine capacities, with notable enhancements in economic and environmental performance achieved by selecting a 3,250 kW gas engine within the CCHP-desalination system. This choice not only maximizes the annual profit but also reduces CO2 emissions by 57% compared to conventional systems, underscoring the system's sustainability benefits.

Early diversification of membrane intrinsic proteins (MIPs) in eukaryotes.

Membrane intrinsic proteins (MIPs), including aquaporins (AQPs) and aquaglyceroporins (GLPs), form an ancient family of transporters for water and small solutes across biological membranes. The evolutionary history and functions of MIPs have been extensively studied in vertebrates and land plants, but their widespread presence across the eukaryotic tree of life suggests both a more complex evolutionary history and a broader set of functions than previously thought. That said, the early evolution of MIPs remains obscure. The presence of four AQP and one GLP clades across both Bacteria and Archaea suggests that the first eukaryotes could have possessed up to five MIPs. Here, we report on a previously unknown richness in MIP diversity across all major eukaryotic lineages, including unicellular eukaryotes, which make up the bulk of eukaryotic diversity. Three MIP clades have likely deep evolutionary origins, dating back to the last eukaryotic common ancestor (LECA), and support the presence of a complex MIP repertoire in early eukaryotes. Overall, our findings highlight the growing complexity of the reconstructed LECA genome: the dynamic evolutionary history of MIPs was set in motion when eukaryotes were in their infancy followed by radiative bursts across all main eukaryotic lineages.