The potential of Gd doping as a promising approach for enhancing the adsorption properties of nickel-cobalt ferrites.

The study shows that the addition of gadolinium ions has a significant impact on the structure, morphology, and adsorption properties of Ni-Co spinel ferrite that was synthesized by the sol-gel auto-combustion method. The research also indicates that the higher the Gd content, the greater the increase in the lattice parameter, which suggests that Gd3+ ions uniformly replaced the octahedral Fe3+ ions. The morphology and chemical composition of Gd-doped Ni-Co ferrites have been studied using SEM and EDS. Gd adding to the NiCoFe matrix increases the BET surface area by 50% (from 48 to 72 m2/g) and promotes the formation of mesopores with an average radius from 3.9 to 4.9 nm. The pHPZC values of Gd-doped ferrites are in the range of 7.22-7.39, which means that the ferrite surface will acquire a positive charge at natural pH, so this will promote the adsorption of Congo red anionic dye through electrostatic interaction forces. Langmuir, Freundlich, and Dubinin-Radushkevich models were used to explain the mechanism of CR adsorption on the Ni0.5Co0.5GdxFe2-xO4 adsorbent surface. The ionic-covalent parameter has been estimated to describe the surface acid-base properties. Overall, this study highlights the potential of Gd3+ doping as a promising approach for enhancing the adsorption properties of nickel-cobalt ferrites.

On-site extraction of phenoxycarboxylic acid herbicides in environmental waters utilizing monolith-based in-tip microextraction technique.

On-site extraction plays a significant role in the reliable quantification of strong polar phenoxycarboxylic acid herbicides (PCAs) in aqueous samples. In current study, a new technique for the field sample preparation of PCAs was developed by means of three channels in-tip microextraction device (TCIM). To capture PCAs effectively, an extraction phase based on monolith (EPM) using vinylimidazole and divinylbenzene/ethylene dimethacrylate as monomer and cross-linkers, respectively, was in-situ synthesized in pipette tips. The EPM fabricated at optimal conditions were characterized by a series of techniques and employed as the adsorbent of TCIM for the on-site extraction of PCAs. The adsorption isotherm was studied so as to inspect the extraction behaviors of EPM towards PCAs. Results revealed that the proposed EPM/TCIM presented satisfactory extraction performance towards PCAs through multiple interactions. The enrichment factors and adsorption capacity were 74-277 and 20 mg g-1, respectively. Under the most beneficial extraction parameters, the developed EPM/TCIM was successfully employed to on-site extract PCAs, and then combining with HPLC equipped with diode array detector to monitor trace PCAs in actual waters. The limits of detection (LODs) towards investigated PCAs varied from 0.071 µg/L to 0.30 µg/L. In addition, the accuracy of established approach was inspected with documented method. Compared with existing lab-based sample preparation approaches, the introduced field sample preparation technique exhibits some merits such as avoidance of transporting large volume of water, prevention of analytes loss during sampling procedure, less usage of organic solvent and achievement of satisfactory efficient in sample preparation.

Efficient adsorption of acid orange 7 from wastewater using novel bio-natural granular bentonite-sawdust-corncob (GBSC): Mixture optimization, adsorption kinetic and regeneration.

The removal of dyes from industrial wastewater is one of the most environmental challenges that should be addressed through sustainable technologies. In this study, a novel green and cost-effective granular from bentonite and bio-wastes of sawdust and corncob (GBSC) was prepared for sustainable treatment of acid orange 7 (AO7) dye wastewater. The d-optimal mixture method was employed to determine the optimum combination of the GBSC in terms of dye adsorption and structure stability. Characterizations of the GBSC were investigated using SEM, XRD, FTIR and BET analyses and compared with bentonite powder (BP), modified bentonite powder (MBP), and granular modified bentonite (GMB). According to the results, a mixture of bentonite 60 wt.%, sawdust 20 wt.% and corncob 20 wt.% at 550°C yielded the optimal combination of the GBSC which resulted to the highest adsorption capacity 135.22 mg/g, the lowest mass loss 3.1% and maximum crushing strength 12.275 N. The kinetic and isotherm of the adsorption data were fitted well by the pseudo-second-order model and Langmuir isotherm. Our finding suggested a green circular economy model by utilizing agriculture wastes (sawdust and corncob) to synthesize GBSC for sustainable dye wastewater treatment, which offers a cost-effective adsorbent (0.907 $/g) with high regeneration (4 times reusability with 40.5% removal rate) to keep them in circulation for as long as possible.

Carbon dots-loaded cellulose nanofibrils hydrogel incorporating Bi2O3/BiOCOOH for effective adsorption and photocatalytic degradation of lignin.

A novel photocatalytic adsorbent, a cellulose nanofibrils based hydrogel incorporating carbon dots and Bi2O3/BiOCOOH (designated as CCHBi), was developed to address lignin pollution. CCHBi exhibited an adsorption capacity of 435.0 mg/g, 8.9 times greater than that of commercial activated carbon. This enhanced adsorption performance was attributed to the 3D porous structure constructed using cellulose nanofibrils (CNs), which increased the specific surface area and provided additional sorption sites. Adsorption and photocatalytic experiments showed that CCHBi had a photocatalytic degradation rate constant of 0.0140 min-1, 3.1 times higher than that of Bi2O3/BiOCOOH. The superior photocatalytic performance of CCHBi was due to the Z-scheme photocatalytic system constructed by carbon dots-loaded cellulose nanofibrils and Bi2O3/BiOCOOH, which facilitated the separation of photoinduced charge carriers. Additionally, the stability of CCHBi was confirmed through consecutive cycles of adsorption and photocatalysis, maintaining a removal efficiency of 85 % after ten cycles. The enhanced stability was due to the 3D porous structure constructed by CNs, which safeguarded the Bi2O3/BiOCOOH. This study validates the potential of CCHBi for high-performance lignin removal and promotes the application of CNs in developing new photocatalytic adsorbents.

Superparamagnetic composites of lignin regenerated from ionic liquid solutions for the efficient and selective removal of cationic dyes.

Magnetic lignin nanoparticles (MLNs) were prepared by inducing their self-assembly through lignin regeneration in the [N-methyl-2-pyrrolidone][C1-C4 carboxylic acid] ionic liquids ([NMP]ILs), which are low-cost protic ionic liquid. [NMP]ILs are self-assembling solvent that can enhance the adsorption capacity of MLNs to a greater degree than tetrahydrofuran or H2O. Additionally, the anion types of [NMP]IL greatly influence the physiochemical properties of MLNs. The MLNs prepared through self-assembly with [NMP][formate] (MLN/[NMP][For]) exhibited a higher maximum adsorption capacity (134.53 mg/g) than the [NMP]ILs of C2-C4 carboxylate anions. MLN/[NMP][For] demonstrated stable adsorption within a pH range of 6-10 or at high salt concentrations (0.01-0.5 mol/L), retaining over 80 % of its regeneration efficiency after 5 cycles. In addition, MLN/[NMP][For] selectively removed cationic dyes in mixed binary anionic-cationic dye solutions. This work demonstrated the feasibility of preparing magnetic biosorbents with good selectivity and stability though regeneration and by adjusting the anions of ionic liquids.

A novel approach for the modification of eggshell powder and its application for lead and methylene blue removal.

Water pollution is one of the major concerns due to rapid industrialization and urbanization. Wastewater treatment has been an area of great interest for the researchers and among many technologies developed for water treatment, adsorption is the most preferred due to its efficiency and ability of been economical method. In this research, eggshell powder (ESP) is converted into modified eggshell powder (MESP) through chemical and thermal treatment (at 550 °C for 2 h) to use it as an adsorbent to remediate Pb2+ and Methylene blue (MB) from water, then it is transferred into modified eggshell powder magnetic composite (MESPMC) with iron coating to resolve the separation challenges and to boost the MESP's adsorption efficiency. FTIR analysis identified the functional groups of ESP, MESP, and MESPMC. XRD analysis reveals a hexagonal crystal structure of calcite in MESP and a combination of the hexagonal crystal structure of calcite and the cubic crystal structure of iron in MESPMC. The Scherrer equation is used to determine the average crystallite sizes of MESP and MESPMC, which are 22.59 nm and 12.15 nm, respectively. The SEM image shows the irregular shape of the MESP and MESPMC particles, as well as the active coating layer in MESPMC. EDX analysis reveals that Ca (20.92 %), O (56.83 %), and Fe (41.03 %), O (48.83 %) are the most abundant elements in MESP and MESPMC respectively. TGA analysis points out that MESPMC outperforms MESP in terms of thermal stability between 600 and 750 °C. MESP and MESPMC were found to be very efficient adsorbent for lead and methylene blue in aqueous medium. At 40 mg/mL adsorbent dosage, ESP, MESP, and MESPMC had the highest yields of Pb2+ removal, with 46.996 %, 99.27 %, and 99.78 % respectively at 200 rpm for 60 min with 25 °C. Furthermore, at the 0.5 mg/mL adsorbent dosage, ESP, MESP, and MESPMC have the maximum removal efficiency of methylene blue, with 47.19 %, 90.1 %, and 92 %, respectively at 200 rpm for 30 min with 25 °C. In both cases, the removal efficiency of MESPMC is slightly higher than that of MESP and much higher than that of ESP. Additionally, the results confirm that MESP and MESPMC are potential environment-friendly bio sources to remediate heavy metal (Pb2+) and methylene blue dye from water.

Nano-tentacled interconnected channels organic gel for rapid uranium extraction from seawater.

Due to dwindling terrestrial uranium resources and escalating ecological pressures, the long-term viability of uranium supply has become a critical concern. The immense uranium reserves in seawater present a potential solution, yet extraction technology faces dual challenges of efficiency and adaptability to complex marine environments. Current interconnected porous adsorbents, despite their high flux properties, are limited by low specific surface area and weak mechanical strength, which constrain their effectiveness. Here, inspired by the unique hierarchical structures of marine organisms, we describe an organic gel adsorbent with supermacroporous and interconnected channels (10 ∼ 100 µm) adorned with "nano-tentacle" structures. This design significantly enhances the specific surface area by 18 times, increasing adsorption sites and imparting antibacterial properties. Notably, this adsorbent maintains structural integrity and superior mechanical strength (1.32 MPa tensile and 2.44 MPa compressive strength) even when fully saturated. During a 23-day trial in natural seawater, a uranium adsorption rate of 0.332 mg g⁻¹ day⁻¹ was achieved. This work offers a pioneering approach for the design and fabrication of hierarchical structured adsorbents, highlighting the immense potential of extracting uranium from seawater for sustainable energy production.

Facile synthesis of ATTM@ZIF-8 modified pullulan hydrogels for enhanced adsorption of Congo red and malachite green.

Efficient capture of dyes from wastewater is of great importance for environmental remediation. Yet constructing adsorbents with satisfactory adsorption efficiency and low cost remains a major challenge. This work reports a simple and scalable method for the fabrication of functionalized porous pullulan hydrogel adsorbent decorated with ATTM@ZIF-8 for the adsorption of congo red (CR) and malachite green (MG). The embedding of ammonium tetrathiomolybdate (ATTM) into the ZIF-8 nanoclusters offered additional adsorption sites and enlarged the pore size of the resulting ATTM@ZIF-8. The homogeneous dispersion of the nanoparticles in the three-dimensional network of polysaccharide gels prevents their agglomeration and thus improves the affinity for dye molecules. The resulting adsorbent AZP-20 at optimized composite ratios exhibits high activity, selectivity, interference resistance, reusability and cytocompatibility in dye adsorption applications, and possesses high removal rate of dye in real water systems. Batch experiments demonstrated that the adsorption rate of AZP-20 for MG and CR was 1645.28 mg g-1 and 680.33 mg g-1, and would be influenced by pH conditions. Adsorption kinetics followed pseudo-second-order model. Adsorption isotherms followed Langmuir model for MG and Freundlich model for CR. The adsorption of dye molecules primarily relied on electrostatic interaction (MG) and π-π stacking interaction (CR). Conclusively, the prepared AZPs adsorbent illuminated good application prospects in the treatment of complex component dye wastewater.

Discovery of a new volcanic soil material, "Akahoya," as an adsorbent for bacterial and viral pathogens and its application to environmental purification.

Akahoya is a volcanic soil rich in alumina, primarily deposited in Kyushu, Japan. We have found that Akahoya adsorbs bacteria in the water surrounding cattle grazing areas, suggesting a potential for environmental purification. This study investigated the spectrum of microorganisms adsorbed by Akahoya using a column filled with Akahoya through which a suspension of microorganisms was passed. Shirasu soil, another volcanic soil with a different chemical composition, was used as a control. Akahoya effectively adsorbed a diverse range of microorganisms including Escherichia coli, Campylobacter jejuni, Vibrio parahaemolyticus, Salmonella Enteritidis, Staphylococcus aureus, Clostridium perfringens, spores of Bacillus subtilis and Bacillus anthracis, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), murine norovirus, and avian influenza virus (H3N2), whereas Shirasu soil did not adsorb any of the organisms examined. Moreover, bacteria naturally present in river water, such as aerobic bacteria, total coliforms, and Enterobacteriaceae as indicators of river contamination, as well as E. coli added artificially to sterilized river water, were reduced to below the detection limit (<1 CFU/mL) after being passed through Akahoya. Additionally, the number of viable E. coli continued to decrease after contact with Akahoya for 1 month, suggesting bactericidal effects. Notably, the adsorption of E. coli to Akahoya was influenced by the concentration of phosphate and the pH of the suspension due to the interaction between the surface phosphorylation of organisms and Al2O3, the major chemical component of Akahoya. The present results demonstrate the remarkable ability of Akahoya to remove phosphate and microbes, suggesting that Akahoya could be used for water purification processes.IMPORTANCEAlthough a safe and sufficient water supply is essential for the maintenance of hygienic conditions, a major challenge is to develop a comprehensive effective, sustainable, and cost-effective technological approach for the treatment and purification of contaminated water. In this study, we demonstrated that a novel volcanic soil, Akahoya, which has unlimited availability, is a highly effective adsorbent for a wide range of bacterial and viral pathogens, suggesting its potential as a sustainable resource for this purpose. It was suggested that the adsorption of microorganisms on Akahoya was mediated by phosphate groups present on the surface structures of microorganisms, which bind to the alumina component of Akahoya according to the phosphate concentration and pH of the liquid phase. The present findings highlight the exceptional ability of Akahoya to eliminate or reduce phosphate and microorganisms effectively in water purification processes, thus contributing to the development of efficient and sustainable solutions for addressing water pollution challenges.

Silicone-modified black peanut shell (BPS) biochar adsorbents: Preparation and their adsorptions for copper(II) from water.

Novel silicone-modified biochar adsorbents (BPS-MBCs) were prepared by utilizing waste black peanut shell (BPS) as a raw biochar and gamma-amino-propyl triethoxysilane (silicone) as an inorganic modifier. The novelty of this work is that the incorporation of silicone into BPS can rise the specific surface area and porosity of BPS-MBCs and elevate their adsorptions for copper (II). Sorption kinetics data for copper (II) were molded using five kinetic equations [i.e. Lagergren 1st-order and 2nd-order, intraparticle diffusion (IN-D), Elovich, and Diffusion-chemisorption]. The equilibrium adsorption data for copper (II) were analyzed using two-parameter isotherm equations [i.e. Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin] and three-parameter Sips, Redlich-Peterson and Toth isotherm models. It was validated that copper (II) sorption on BPS-MBCs matched better with pseudo-2nd-order kinetic, Diffusion-chemisorption and Langmuir isotherm models. The maximal qmLan of BPS-MBC-400 was near 284 mg/g at 45 °C. By multi-phase fitting of IN-D modelling, intra-particle diffusion coefficient (kin-d) and diffusion coefficient of external mass-transfer (DEx-Di) for copper (II) were calculated. The low sorption energy from Temkin and mean free energy from D-R modellings implied that copper (II) sorption was initiated by weak non-covalent bond interactions. Thermodynamic parameters indicated that copper (II) on BPS-MBCs was an endothermic and spontaneous process. Recycling of BPS-MBC-400 for copper (II) suggested it has excellent reusability. The major mechanism of copper (II) on BPS-MBCs is possibly comprised of multiple processes, such as physical adsorption (electrostatic attraction), chemical adsorption (adsorption from functional groups, chelation, and ion exchange) and diffusion-chemisorption. Based on these findings, it is expects that BPS-MBCs are promising sorbents for copper (II) eradication from Cu(II)-including wastewater.

Fabricating whole pine needles biomass with phenylhydrazine-4-sulphonic acid for effective removal of cationic dyes and heavy metal ions from wastewater.

We applied a holistic, sustainable, and green approach to develop an effective multipurpose adsorbent from whole pine needles (PNs), a forest waste lignocellulosic biomass. The PNs were oxidized and modified with phenylhydrazine-4-sulphonic acid (ɸHSO3H) to OPN-ɸHSO3H. The latter was characterized and tested as an adsorbent for cationic dyes, malachite green (MG), methylene blue (MB), crystal violet (CV), and metal ions (Hg2⁺ and Pb2⁺). The adsorption followed different kinetic models: Elovich for MG and MB, pseudo-second-order for CV, and pseudo-first-order for Hg2⁺ and Pb2⁺. Langmuir isotherm indicated maximum adsorption capacities of 303.4 ± 8.91 mgg-1 (MG), 331.4 ± 17.50 mgg-1 (MB), 376.6 ± 22.47 mgg-1 (CV), 210.8 ± 28.86 mgg-1 (Hg2⁺), and 172.9 ± 20.93 mgg-1 (Pb2⁺) within 30 min. Maximum removal efficiencies were 99.0% (MG), 98.0% (MB), 96.04% (CV), 95.5% (Hg2⁺), and 89.8% (Pb2⁺). The adsorbent demonstrated significant regeneration and reusability over ten cycles, proving highly efficient for both cationic dyes and metal ions, with wide potential for practical applications where more than one adsorbate is present.

One-pot fabrication of task specific magnetic adsorbent for the efficient isolation and capture of liquid-crystal monomers pollutants in waters prior to chromatographic quantification.

BACKGROUND: Liquid crystal monomers (LCMs) have been classified as emerging organic pollutants. Efficient isolation and extraction is a critical step in the determination, and then knowing the occurrence and distribution of LCMs in environmental waters. However, the reported sample preparation techniques still suffer some dilemmas such as using large amount of organic solvent, low extraction capacity, tedious operation procedure and employment of expensive extraction column. To circumvent the disadvantages, new extraction format and adsorbent with quickness, less consumption of organic solvent, superior extraction performance and low cost should be developed for the analysis of LCMs. RESULTS: Using 1H,1H,2H,2H-heptadecafluorodecyl acrylate and 9-vinylanthracene as mixed functional monomers, a task specific magnetic adsorbent (TSMA) was prepared by one-pot hydrothermal technique for the highly efficient capture of LCMs under magnetic solid phase extraction (MSPE) format. Due to the abundant functional groups, the developed TSMA/MSPE presented satisfactory capture performance towards LCMs. Satisfactory enrichment factors (132-212) and high adsorption capacity (18 mg/g) were obtained. Additionally, the relevant adsorption mechanism was studied by the combination of density functional theory calculation and experiments about adsorption kinetics and adsorption isotherm. Under the beneficial conditions, a sensitive and reliable method for the monitoring of studied LCMs in environmental waters was established by the combination of TSMA/MSPE with HPLC equipped with diode array detector (DAD). The achieved limits of detection and spiked recoveries were 0.0025-0.0061 µg/L and 81.0-112 %, respectively. Finally, the developed method was employed to monitor LCMs levels in the North Creek watershed of Jiulong River. SIGNIFICANCE AND NOVELTY: The current study provided a new adsorbent for quick and efficient capture of LCMs at trace levels. In addition, a sensitive, reliable and anti-intereference method for the monitoring of trace LCMs in actual waters was established. Moreover, for the first, the contents, occurrence and distribution of LCMs in North Creek watershed was investigated based on the developed method.

Investigation of the potential of pomegranate peel as a treatment option for heavy metal contaminated wastewater: Experimental and modeling approaches.

Heavy metals can cause serious environmental and human health problems, and their removal from wastewater is critical to protect our planet and communities. This study investigated the ability of crushed pomegranate peel to remove mercury and cadmium ions from contaminated water as a function of different experimental parameters. The experimental results showed that the pH of the solution influenced the adsorptive removal of heavy metals, with the best performance observed at pH 4.8. Optimization studies and process balance modeling were performed to optimize the process for commercial use. The performance of pomegranate peel was compared with that of other materials, and the highest adsorption capacities for both cadmium (Ca (II)) and mercury (Hg (II)) ions were observed to be 89.59 and 42.125 mg/g, respectively. The results were interpreted using the Langmuir model, which provided the best fit to describe the behavior of the process.

Hydrothermal chemical modification of red mud for efficient adsorption of methylene blue.

Red mud (RM) is the industrial solid waste produced after alumina extraction from bauxite, and most RM is directly discharged to the landfill yards without any treatment. In this study, modified red mud (MRM) was synthesized by a hydrothermal chemical modification method as an efficient adsorbent for methylene blue (MB) removal. The prepared MRM was characterized by X-ray fluorescence spectroscopy, X-ray diffraction, scanning electron microscope, transmission electron microscope, and Fourier transform infrared spectrometer. The effects of reaction time, initial MB concentrations, MRM dosage, temperature, and system pH were investigated in the MB batch adsorption experiments. The results showed that the modification method increased the specific surface area of RM material from 16.72 to 414.47 m2/g. The maximum adsorption capacity of MRM for MB was 280.18 mg/g under the conditions of initial MB concentration of 1000 mg/L, reaction time of 300 min, temperature of 25 ℃, and natural pH of 6.06. Meanwhile, the adsorption kinetics and equilibrium isotherms were demonstrated to fit well with the pseudo-second-order kinetic model and Temkin isotherm, respectively. This study provides a new method for the valorization of RM and demonstrates that MRM can be used as a low cost and environmentally friendly potential adsorbent for the removal of MB from wastewater.

[Determination of 13 perfluorinated and polyfluoroalkyl substances in fishes by QuEChERS-ultra-high performance liquid chromatography-tandem mass spectrometry].

Perfluorinated and polyfluoroalkyl substances (PFASs) are compounds characterized by at least one perfluorinated carbon atom in an alkyl chain linked to side-chain groups. Owing to their unique chemical properties, these compounds are widely used in industrial production and daily life. However, owing to anthropogenic activities, sewage discharge, surface runoff, and atmospheric deposition, PFASs have gradually infiltrated the environment and aquatic resources. With their gradual accumulation in environmental waters, PFASs have been detected in fishes and several fish-feeding species, suggesting that they are bioconcentrated and even amplified in aquatic organisms. PFASs exhibit high intestinal absorption efficiencies, and they bioaccumulate at higher trophic levels in the food chain. They can be bioconcentrated in the human body via food (e. g., fish) and thus threaten human health. Therefore, establishing an efficient analytical technique for use in analyzing PFASs in typical fish samples and providing technical support for the safety regulation and risk assessment of fish products is necessary. In this study, by combining solvent extraction and magnetic dispersion-solid phase extraction (d-SPE), an improved QuEChERS method with ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was developed for the determination of 13 PFASs in fish samples. Fe3O4-TiO2 can be used as an ideal adsorbent in the removal of sample matrix interference and a separation medium for the rapid encapsulation of other solids to be isolated from the solution. Based on the matrix characteristics of the fish products and structural properties of the target PFASs, Fe3O4-TiO2 and N-propyl ethylenediamine (PSA) were employed as adsorbents in dispersive purification. The internal standard method was used in the quantitative analyses of the PFASs. To optimize the sample pretreatment conditions of analyzing PFASs, the selection of the extraction solvent and amounts of Fe3O4-TiO2 and PSA were optimized. Several PFASs contain acidic groups that are non-dissociated in acidic environments, thus favoring their entry into the organic phase. In addition, acidified acetonitrile can denature and precipitate the proteins within the sample matrix, facilitating their removal. Finally, 2% formic acid acetonitrile was used as the extraction solvent, and 20 mg Fe3O4-TiO2, 20 mg PSA and 120 mg anhydrous MgSO4 were used as purification adsorbents. Under the optimized conditions, the developed method exhibited an excellent linearity (R≥0.9973) in the range of 0.01-50 µg/L, and the limits of detection (LODs) and quantification (LOQs) ranged from 0.001-0.023 and 0.003-0.078 µg/L, respectively. The recoveries of the 13 PFASs at low, medium, and high spiked levels (0.5, 10, and 100 µg/kg) were 78.1%-118%, with the intra- and inter-day precisions of 0.2%-11.1% and 0.8%-8.7%, respectively. This method was applied in analyzing real samples, and PFASs including perfluorooctanesulfonic acid, perfluorooctanoic acid, perfluoroundecanoic acid, perfluorododecanoic acid, and perfluorotridecanoic acid, were detected in all 11 samples evaluated. This method is simple, sensitive, and suitable for use in analyzing PFASs in fish samples.

The development of Giant reed biochar for adsorption of Basic Blue 41 and Eriochrome Black T. azo dyes from wastewater.

The textile industry is discharging high concentrations of anionic and cationic azo dyes into the nearby environment, which can cause adverse effects on public health, and the aquatic environment. Therefore, this study aimed to develop giant reed biochar and apply for the removal of Basic blue 41 (BB41) and Eriochrome black T (EBT) azo dyes from water. Characterization techniques such as BET surface area analyzer, Fourier-transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermal gravimetric analyzer (TGA) were applied for biochar description. The biochar exhibits a high fixed carbon content (80.4%), a low ash content (3.8%), a large surface area (429.0 m2/g), and good thermal stability. High removal efficiencies of BB41 98.6% and EBT 82.5% were recorded at the specific experimental condition. The experimental data were fitted with the Langmuir isotherm model at R2 0.99 for both dyes whereas the adsorption kinetics revealed the pseudo-second-order kinetics at R2 ∼ 1 and 0.99 for BB41 and EBT, respectively. Furthermore, four regenerations of biochar with adsorption performances of BB41 and EBT dyes were found to be 94.7% and 79.1%, respectively. Finally, this adsorbent can be considered an economically viable material for the removal of synthetic dyes from wastewater systems. In conclusion, the study findings showed that the adsorbent material is promising to apply for water and wastewater treatment but still, the study of adsorption interaction and modifications of the surface functionalities are essential to accommodate multipollutant removal from real water systems.

Effect of modified Ca-Al adsorbents on heavy metal fixation during co-combustion of coal and coconut shells: Experiments and simulations.

As an alternative fuel, bio-waste coconut shells have shown promise in reducing pollution during the co-combustion process. In this study, a novel metal-mineral adsorbent, Ca-Al (Ca5Al6O14), was prepared and physically (ultrasonic) and chemically (ethylene glycol) modified to enhance its adsorption properties. Thermal adsorption experiments investigated the effect of the adsorbents on the fixation of six heavy metals (HMs): Cr, Cu, Mn, Ni, Pb, and Zn. XRD, SEM, BET, and XPS were used to analyze the adsorbents and the adsorption mechanism was investigated by combining lattice oxygen concentration and Factsage simulation calculations. The ecological risk assessment of heavy metals was used to comprehensively evaluate the fixation effects of the three Ca-Al adsorbents at different additive levels. The results showed that the modification significantly changed the morphological characteristics and oxygen activity of the Ca-Al adsorbents, increased the lattice oxygen and chemisorbed oxygen concentration, and laid the foundation for promoting the chemisorption process in the fixation of heavy metals. In combination with the Er (environmental risk factors), adding all three adsorbents reduced Ri (Risk index). Among them, Ca-Al (EG) at 3% had the best effect on Ri. 3% Ca-Al (EG) reduced the Er value of Ni by 49.02%. 5% Ca-Al (EG) reduced the Er value of Cr by 86.01%. 5% Ca-Al (UM) had the best effect on Mn, with a reduction of 46.13%. The addition of 10% Ca-Al (UM) reduced Er of Ni by 50.43%. Considering the practical application in coal-fired power plants, Ca-Al(EG), which exhibits a higher fixation rate at small additions, is more suitable.

Development of Zeolite Imidazole Framework-Based Adsorbent for Effective Microextraction and Preconcentration of Histamine in Food Samples.

This study is the first to focus on the preconcentration and determination of histamine (HIS) in food samples using zeolite imidazole frameworks (ZIFs) on a solid-phase microextraction (SPME) platform. ZIF was developed on a polypropylene hollow fiber (PPHF) substrate (ZIF@PPHF) and characterized. The extraction performance was optimized by adjusting several parameters, including pH, contact time for adsorption, and desorption conditions. Under the optimized conditions, a wide linear dynamic range (0.05-250 mg/L) with high R2 values (0.9989), low limit of detection (0.019 mg/L), and low limit of quantification (0.050 mg/L) were determined as analytical figures of merit. Additionally, a reusability study confirmed that ZIF@PPHF preconcentrated 83% of the HIS up to the fourth cycle. The developed method was used to preconcentrate HIS in fish and cheese samples. The spiked real samples confirmed the validity and accuracy of this method. The percentage mean recoveries ± relative standard deviation (% RSD, n = 3) at the concentration levels of 5, 10, and 50 mg/L of HIS and the sample amount of 5 g for intra- and inter days ranged from 97 ± 1.10 to 102.80 ± 0.90 and from 96.40 ± 1.82 to 103.40 ± 0.79, respectively. The results suggest that the analytical method validation parameters were acceptable, indicating the repeatability and sensitivity of the method.

Development and Evaluation of a Dry Emulsion of Ostrich Oil as a Dietary Supplement.

This study aimed to develop a high-quality dry emulsion incorporating omega-3, 6, and 9 fatty acid-rich ostrich oil for use as a dietary supplement. Extracted from abdominal adipose tissues using a low-temperature wet rendering method, the ostrich oil exhibited antioxidant properties, favorable physicochemical properties, microbial counts, heavy metal levels, and fatty acid compositions, positioning it as a suitable candidate for an oil-in-water emulsion and subsequent formulation as a dry emulsion. Lecithin was employed as the emulsifier due to its safety and health benefits. The resulting emulsion, comprising 10% w/w lecithin and 10% w/w ostrich oil, was stable, with a droplet size of 3.93 ± 0.11 µm. This liquid emulsion underwent transformation into a dry emulsion to preserve the physicochemical stability of ostrich oil, utilizing Avicel® PH-101 or Aerosil® 200 through a granulation process. Although Aerosil® 200 exhibited superior adsorption, Avicel® PH-101 granules surpassed it in releasing the ostrich oil emulsion. Consequently, Avicel® PH-101 was selected as the preferred adsorbent for formulating the ostrich oil dry emulsion. The dry emulsion, encapsulated with a disintegration time of 3.11 ± 0.14 min for ease of swallowing, maintained microbial loads and heavy metal contents within acceptable limits. Presented as granules containing butylated hydroxytoluene, the dry emulsion showcased robust temperature stability, suggesting the potential incorporation of animal fat into dry emulsions as a promising dietary supplement.

Selective recovery of europium from real acid mine drainage using modified Cr-MIL and SBA15 adsorbents.

The successful adoption and widespread implementation of innovative acid mine drainage treatment and resource recovery methods hinge on their capacity to demonstrate enhanced performance, economic viability, and environmental sustainability compared to conventional approaches. Here, an evaluation of the efficacy of chromium-based metal-organic frameworks and amine-grafted SBA15 materials in adsorbing europium (Eu) from actual mining wastewater was conducted. The adsorbents underwent comprehensive characterization and examination for their affinity for Eu. Cr-MIL-PMIDA and SBA15-NH-PMIDA had a highest Langmuir adsorption capacity of 69 mg/g and 86 mg/g, respectively, for an optimum level of pH 4.8. Preferential adsorption tests followed using real AMD collected at a disused mine in the north of Norway. A comparative study utilizing pH-adjusted real AMD revealed that Cr-MIL-PMIDA (88%) exhibited slightly higher selectivity towards Eu compared to SBA15-NH-PMIDA (81%) in real mining wastewater. While Cr-MIL-PMIDA displays excellent properties for the selective recovery of REEs, practical challenges related to production costs and potential susceptibility to chromium leaching make it less appealing for widespread applications. A cost-benefit analysis was then undertaken to quantify the advantages of employing SBA15-NH-PMIDA material. The study disclosed that 193.2 g of EuCl3 with 99% purity can be recovered by treating 1000 m3 of AMD.