Magnetic Fe3O4 /Al2O3 /MnO2 ternary nanocomposite: Synthesis and characterization for phosphorus desorption from acidic soils using dialysis membrane tube.

Monitoring phosphorus fertilization is crucial for controlling the concentration of biologically available soil P. Over the years, several methodologies have been used, including successive cropping in a greenhouse or field, as well as extractions employing P sink procedures. The latter procedures are ideal laboratory experiments to show the soil's ability to supply P and to explore the P-residual release kinetics. Following these methodologies, long-term P desorption studies have been developed using dialysis membrane tubes filled with nanomaterial solutions. In this study, a magnetic nanocomposite (Fe3O4/Al2O3/MnO2) was synthesized and characterized utilizing cutting-edge instruments such as XRD, FTIR, FAAS, BET, SEM, and EDX. The resulting material had a crystalline size and surface area of 22.75 nm and 203.69 m2/g, respectively, and was employed for long-term P-desorption and kinetics experiments while filled in dialysis membrane tubes. The P-desorption experiment was conducted on four separate acidic soil samples that were cultured for 122 days with four different P concentrations. The findings demonstrated a direct relationship between P-desorbed and P-treatment, as well as with desorption time. The minimum desorption was obtained from the control of Boji Dirmaji soil P0 (1.16-9.36) and the highest desorption from Nedjo soil with P3 (5.23-30.35 mg/kg) treatment over 1-28 days. The rate of P release from soil to solution or diffusion through the membrane was determined by pseudo-first-order kinetics with a rate constant (0.021-0.028 hr-1). This method has the potential to measure fixed-P availability by mimicking it as a plant would, with high P-desorption efficiency and quick P-release capacity.

The non-edible and disposable parts of oyster mushroom, as novel adsorbent for quantitative removal of atrazine and its degradation products from synthetic wastewater.

In this study, the non-edible part of oyster mushroom was utilized for quantitative removal of the most commonly used s-triazine herbicide; atrazine and its breakdown products including deethylatrazine (DEA), hydroxyatrazine (ATOH) and deisopropylatrazine (DIA) from aqueous samples. The functional groups available on the oyster mushroom were studied applying FTIR before and after adsorption. Experimental parameters influencing the uptake process including acidity, sorbent mass, sorption time, initial analyte quantities, and agitation speed were analysed and the maximum removal was found at 4, 0.3 g, 120 min, 0.5 mg L-1, and 150 rpm, respectively. Accordingly, the adsorption capacities of 0.994, 1.113, 0.991 and 1.016 mg g-1 were obtained for DIA, DEA, ATOH and atrazine, respectively. The adsorption characteristics were discussed utilizing Langmuir and Freundlich isotherm models. The fundamental characteristic of the Langmuir isotherm, which can be elaborated using separation factor or equilibrium parameter, RL, and coefficient of variation, R2, were (0.761, 0.996), (0.884, 0.975), (0.908, 0.983) and (0.799, 0.984) for DIA, DEA, ATOH and Atrazine, respectively. These findings showed that all analytes' adsorption processes were fitted well to the Langmuir adsorption isotherm, indicating that the adsorbent surface was covered in a monolayer. The kinetics was also evaluated using the pseudo-first and pseudo-second order models. The coefficient of determination, r2, were found to be 0.09703, 0.9989, 0.9967 and 0.9998 for DIA DEA, ATOH and atrazine, respectively, for pseudo-second order, signifying that, all analytes were found to follow the pseudo-second order rate model showing that the rate limiting step is chemisorption in the sorption process. Based on these findings, the non-edible and disposable part of the oyster mushrooms can be utilized as a preferred alternative biosorbent for the uptake of the target compounds analysed and other pollutants possessing comparable physicochemical characteristics occurring in various water bodies.

Impact of source water quality on total organic carbon and trihalomethane removal efficiency in a water treatment plant: A case study of Upper Awash, Ethiopia.

This study addresses the limited understanding of factors affecting the efficiency of water treatment plants in reducing trihalomethane (THM) formation through total organic carbon (TOC) removal, highlighting significant challenges in improving treatment effectiveness. The aim of this study was to examine the influence of water quality on the efficiency of water treatment plants to remove TOC and reduce THM formation. Linear regression and correlation analyses were conducted to examine the relationship between water quality parameters and THM concentrations. The results showed that there was a negative relationship between turbidity, metals, and TOC concentration with TOC removal efficiency. Positive correlations were found between parameters and the formation of THMs in water. Of these parameters, water temperature was observed to have relatively less influence on THM formation. It was observed that seasonal variations in water quality affect the efficiency of TOC removal and THM content in treated water. THM levels in chlorinated water were found to be within the permissible range of the World Health Organization's drinking water quality guidelines. However, it is still important to maintain continuous monitoring and take measures to reduce THMs. The model demonstrated a strong correlation (R2 = 0.906) between predicted and measured THM values.

Plasmon-based colorimetric assay using green synthesized gold nanoparticles for the detection of bisphenol A.

Herein, we report a green synthesized gold nanoparticle (AuNPs) based colorimetric detection of bisphenol A (BPA). The AuNPs were synthesized using khat leaf extract as a reducing agent by optimizing factors affecting the AuNPs synthesis, including gold precursor concentration (1 mM), and reaction temperature (60 °C). The AuNPs characterization was carried out using ultraviolet-visible spectrophotometry and transmission electron microscopy, and it was found spherical with an average particle size of 17.3 ± 3.7 nm. A colorimetric nanosensor was developed by conjugation of bio-inspired AuNPs with BPA-specific aptamer for a quick and easy detection of BPA in plastic bottled water. The colorimetric assay relies on the strong affinity of BPA for aptamer, which causes detachment of the aptamer from the AuNPs surface in the presence of BPA inducing AuNPs aggregation. To achieve the colorimetric detection of BPA, the concentrations of NaCl and aptamer were optimized. The detection of BPA was monitored visually using a naked eye, as well as quantitatively using an ultraviolet-visible spectrophotometer. The method visual limit of detection (LOD) was determined to be 0.1 ng/mL and reached 0.09 ng/mL using ultraviolet-visible spectrophotometer. The method demonstrated very good linearity (R2 = 0.9986) in the range of 0.1-100 ng/mL. The proposed method showed high sensitivity to BPA detection in plastic bottled water with 86.7-98.0%, recovery. Therefore, the proposed colorimetric nanosensor can be used for determination of BPA in plastic bottled waters with reliable performance at lower concentrations.

Contents and health risk assessments of selected heavy metals in vegetables produced through irrigation with effluent-impacted river.

The widely consumed vegetables, khat, lettuce, and Swiss chard, in Hirna town, West Hararghe, Ethiopia, are extensively cultivated through irrigation with an effluent-impacted river that flows through the town which denotes that monitoring the safety of the vegetables is crucial. Herein, the contents of Pb, Zn, Cu, Cr, and Cd in vegetables, water, and soils were determined by flame atomic absorption spectrometry after a wet digestion procedure based on a mixture of HNO3 and HClO4 at 200 °C. pH and electrical conductivity of the water and soil, and health risks associated with vegetable consumption were determined. The pH of the water (6.64) and soil (6.67) was slightly acidic, and electrical conductivity values were 0.416 and 0.024 mS/cm, respectively, indicating both are in good condition. The metal concentrations were in the range of ND-3.12, 3.43-9.22, and 0.15-10.6 mg/L in the water, soil, and vegetables, respectively, and the contents followed a trend of Cu > Zn > Cr > Pb > Cd. The irrigation water contained all metals above the guidelines except Cd, and the soil contained safe levels except Cd which is above the guideline. The obtained metal levels in the vegetables were below the safe limits. Estimated daily intakes and the total target cancer risks were below the guidelines, and the target hazard quotient and the hazard index were below 1 indicating that the vegetables are safe for consumption. In general, the obtained results suggest that the vegetables are safe for consumption. However, continuous monitoring and policy development are required to mitigate contamination of the river.

Preparation and Adsorption Behavior of Ce(III)-MOF for Phosphate and Fluoride Ion Removal from Aqueous Solutions.

The discharge of inorganic pollutants like phosphate and fluoride is a cause of mounting concern to the world due to the substantial environmental and human health risk. Adsorption is one of the most common and affordable technologies widely utilized for removing inorganic pollutants such as phosphate and fluoride anions. Investigating efficient sorbents for the adsorption of these pollutants is extremely important and challenging. This work aimed at studying the adsorption efficiency of the Ce(III)-BDC metal-organic framework (MOF) for the removal of these anions from an aqueous solution using a batch mode. Powder X-ray diffraction (XRD), Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), and scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDX) techniques evidenced the successful synthesis of Ce(III)-BDC MOF in water as a solvent without any energy input within a short reaction time. The outstanding removal efficiency of phosphate and fluoride was exhibited at an optimized pH (3, 4), adsorbent dose (0.20, 0.35 g), contact time (3, 6 h), agitation speed (120, 100 rpm), and concentration (10, 15 ppm) for each ion, respectively. The experiment on the effect of coexisting ions demonstrated that SO42- and PO43- ions are the primary interfering ions in phosphate and fluoride adsorption, respectively, while the HCO3- and Cl- ions were found to have interfered less. Furthermore, the isotherm experiment showed that the equilibrium data fitted well with the Langmuir isotherm model and the kinetic data correlated well with the pseudo-second-order model for both ions. The results of thermodynamic parameters such as ΔH°, ΔG°, and ΔS° evidenced an endothermic and spontaneous process. The regeneration of the adsorbent made using water and NaOH solution showed the easy regeneration of the sorbent Ce(III)-BDC MOF, which can be reused four times, revealing its potential application for the removal of these anions from aqueous environment.

Ionic-liquid-based dispersive liquid-liquid microextraction combined with high-performance liquid chromatography for the determination of multiclass pesticide residues in water samples.

Ionic-liquid-based dispersive liquid-liquid microextraction in combination with high-performance liquid chromatography and diode array detection has been proposed for the simultaneous analysis of four multiclass pesticide residues including carbaryl, methidathion, chlorothalonil, and ametryn from water samples. The major experimental parameters including the type and volume of ionic liquid, sample pH, type, and volume of disperser solvent and cooling time were investigated and optimum conditions were established. Under the optimum experimental conditions, limits of detection and quantification of the method were in the range of 0.1-1.8 and 0.4-5.9 µg/L, respectively, with satisfactory enrichment factors ranging from 10-20. The matrix-matched calibration curves, which were constructed for lake water, as a representative matrix were linear over wide range with coefficients of determination of 0.996 or better. Intra- and interday precisions, expressed as relative standard deviations, were in the range of 1.1-9.7 and 3.1-7.8%, respectively. The relative recoveries of the spiked environmental water samples at one concentration level were in the range of 77-102%. The results of the present study revealed that the proposed method is simple, fast, and uses environmentally friendly extraction solvent for the analysis of the target pesticide residues in environmental water samples.

Trace level enrichment of lead from environmental water samples utilizing dispersive liquid-liquid microextraction and quantitative determination by graphite furnace atomic absorption spectrometry.

Dispersive liquid-liquid microextraction (DLLME) was developed and successfully applied, as a sample preconcentration and extraction method, for the determination of trace quantities of lead (Pb) in environmental water samples utilizing graphite furnace atomic absorption spectrometer (GFAAS). Experimental parameters optimized include; extraction and disperser solvent types and their volumes, pH, extraction period, effect of the co-existing ions and the amount of chelating agent, ammonium pyrrolidine dithiocarbamate (APDC). Under the optimized conditions, enrichment factor of 195 at 5 µg L(-1) level and detection limit of 0.16 µg L(-1) were obtained. Linearity from 25-75 µg L(-1) with R(2) of 0.995 was achieved. The procedure was validated utilizing four environmental water samples at the spiking levels of 10 and 20 µg L(-1) and the corresponding recoveries ranged from 89.6 to 95.1% and 91.6 to 97.1%, respectively, indicating the reliability and applicability of the method for selective extraction of trace level lead.