Elemental composition and potential health risk of vegetable cultivated in residential area situated close to abandoned gold mine dump: Characteristics of soil quality on the vegetables.

The presence of toxic metals in residential areas near abandoned gold mine tailings is a major environmental issue. This study mainly aimed to investigate the elemental distribution of both toxic and essential elements in soils and leafy vegetables (Brassica oleracea) collected from eight different sites around the Davidsonville residential area, located closer to the abandoned Princess gold mine dump, Johannesburg, South Africa. The nutritional value of vegetables in the human diet was determined to assess their value to their health. The vegetables contained metals in the following descending order: Ca > Mg > Ca > Sb > Pb > Fe > Mo > Cr > Se > As > V > Ni > Co > Cd. The bioaccumulation factor (BAF) revealed that vegetables tend to accumulate most metals even (toxic) during the transfer and translocation process. Based on the recommended daily allowance (%RDA) the vegetables showed to contribute 152%, 84% and 75% toward RDA for Se, V and Ca, respectively for most adults and these play a role in human metabolic activities. The vegetables were found to be a good source of essential elements (Ca, Mg, Ni, Na, Fe) but with some traces of toxic metals such as Pb, As and Sb. Based on the health risk assessment, the vegetable posed an adverse health hazard for human consumption due to metals with high HRI >1.

The importance and status of the micronutrient selenium in South Africa: a review.

Selenium (Se) is a vital micronutrient with widespread biological action but leads to toxicity when taken in excessive amounts. The biological benefits of Se are mainly derived from its presence in active sites of selenoproteins such as glutathione peroxidase (GPx). An enzyme whose role is to protect tissues against oxidative stress by catalysing the reduction of peroxidase responsible for various forms of cellular damage. The benefits of Se can be harvested when proper regulations of its intake are used. In South Africa, Se distribution in people's diets and animals are low with socio-economic factors and heterogeneous spread of Se in soil throughout the country playing a significant role. The possible causes of low Se in soils may be influenced by underlying geological material, climatic conditions, and anthropogenic activities. Sedimentary rock formations show higher Se concentrations compared to igneous and metamorphic rock formations. Higher Se concentrations in soils dominates in humid and sub-humid areas of South Africa. Furthermore, atmospheric acid deposition dramatically influences the availability of Se to plants. The studies reviewed in this article have shown that atomic absorption spectroscopy (AAS) is the most utilised analytical technique for total Se concentration determination in environmental samples and there is a lack of speciation data for Se concentrations. Shortcomings in Se studies have been identified, and the future research directions of Se in South Africa have been discussed.

Beta-Cyclodextrin-Decorated Magnetic Activated Carbon as a Sorbent for Extraction and Enrichment of Steroid Hormones (Estrone, ß-Estradiol, Hydrocortisone and Progesterone) for Liquid Chromatographic Analysis.

A ß-cyclodextrin-decorated magnetic activated carbon adsorbent was prepared and characterized using various analytical techniques (X-ray diffraction (XRD), scanning electron microscopy-electron diffraction spectroscopy (SEM-EDS) and transmission electron microscopy (TEM)), and the adsorbent was used in the development of a magnetic solid-phase microextraction (MSPE) method for the preconcentration of estrone, ß-estradiol, hydrocortisone and progesterone in wastewater and river water samples. This method was optimized using the central composite design in order to determine the experimental parameters affecting the extraction procedure. The quantification of hormones was achieved using high-performance liquid chromatography equipped with a photodiode array detector (HPLC-DAD). Under optimum conditions, the linearity ranged from 0.04 to 300 µg L-1 with a correlation of determinations of 0.9969-0.9991. The limits of detection and quantification were between 0.01-0.03 and 0.033-0.1 µg L-1, with intraday and interday precisions at 1.1-3.4 and 3.2-4.2. The equilibrium data were best described by the Langmuir isotherm model, and high adsorption capacities (217-294 mg g-1) were obtained. The developed procedure demonstrated high potential as an effective technique for use in wastewater samples without significant interferences, and the adsorbent could be reused up to eight times.

Adsorptive Removal of Cd, Cu, Ni and Mn from Environmental Samples Using Fe3O4-Zro2@APS Nanocomposite: Kinetic and Equilibrium Isotherm Studies.

In this study, Fe3O4-ZrO2 functionalized with 3-aminopropyltriethoxysilane (Fe3O4-ZrO2@APS) nanocomposite was investigated as a nanoadsorbent for the removal of Cd(II), Cu(II), Mn (II) and Ni(II) ions from aqueous solution and real samples in batch mode systems. The prepared magnetic nanomaterials were characterized using X-ray powder diffraction (XRD), scanning electron microscopy/energy dispersion x-ray (SEM/EDX) Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). Factors (such as adsorbent dose and sample pH) affecting the adsorption behavior of the removal process were studied using the response surface methodology. Under optimized condition, equilibrium data obtained were fitted into the Langmuir and Freundlich isotherms and the data fitted well with Langmuir isotherms. Langmuir adsorption capacities (mg/g) were found to be 113, 111, 128, and 123 mg/g for Cd, Cu, Ni and Mn, respectively. In addition, the adsorption kinetics was analyzed using five kinetic models, pseudo-first order, pseudo-second order, intraparticle diffusion and Boyd models. The adsorbent was successfully applied for removal of Cd(II), Cu(II), Mn (II) and Ni(II) ions in wastewater samples.

In-Syringe Micro Solid-Phase Extraction Method for the Separation and Preconcentration of Parabens in Environmental Water Samples.

In this study, a simple, rapid and effective in-syringe micro-solid phase extraction (MSPE) method was developed for the separation and preconcetration of parabens (methyl, ethyl, propyl and butyl paraben) in environmental water samples. The parabens were determined and quantified using high performance liquid chromatography and a photo diode array detector (HPLC-PDA). Chitosan-coated activated carbon (CAC) was used as the sorbent in the in-syringe MSPE device. A response surface methodology based on central composite design was used for the optimization of factors (eluent solvent type, eluent volume, number of elution cycles, sample volume, sample pH) affecting the extraction efficiency of the preconcentration procedure. The adsorbent used displayed excellent absorption performance and the adsorption capacity ranged from 227⁻256 mg g−1. Under the optimal conditions the dynamic linear ranges for the parabens were between 0.04 and 380 µg L−1. The limits of detection and quantification ranged from 6⁻15 ng L−1 and 20⁻50 ng L−1, respectively. The intraday (repeatability) and interday (reproducibility) precisions expressed as relative standard deviations (%RSD) were below 5%. Furthermore, the in-syringe MSPE/HPLC procedure was validated using spiked wastewater and tap water samples and the recoveries ranged between from 96.7 to 107%. In conclusion, CAC based in-syringe MSPE method demonstrated great potential for preconcentration of parabens in complex environmental water.

Selective and precise solid phase extraction based on a magnetic cellulose gold nanocomposite followed by ICP-OES analysis for monitoring of total sulfur content in liquid fuels.

This study describes the synthesis and characterization of a magnetic cellulose gold nanocomposite (MCNC@Au) for magnetic solid phase (m-SPE) extraction of total sulfur content in liquid fuel samples followed by analysis using inductively coupled plasma-optical emission spectroscopy (ICP-OES). The nanocomposite was prepared using an in situ co-precipitation method and characterization results from FTIR, P-XRD, TEM and SEM-EDX techniques confirmed the formation of the targeted nanocomposite. To achieve good extraction efficiency, the 2-level half-fractional factorial design and central composite design were used to investigate the most influential parameters of the proposed m-SPE method. The multivariate optimization results showed that efficient extraction was obtained when 27.5 mg sorbent mass, 35 minutes sorption time, 200 µL eluent volume and 8 min elution time were used. The optimal parameters resulted in excellent accuracy (98.8%), precision (1.7%), LOD (0.039 mg L-1), LOQ (0.129 mg L-1), MDL (0.014 µg g-1) and MQL (0.047 µg g-1). The optimized and validated m-SPE method was applied in real fuel oil samples, revealing a total sulfur content range of 13.20 ± 0.05-15.70 ± 0.02 µg g-1 for crude oil, 7.32 ± 0.01-9.12 ± 0.03 for µg g-1, 8.41 ± 0.02-9.15 ± 0.06 µg g-1 for gasoline and 9.10 ± 0.02 and 9.70 ± 0.04 µg g-1 for kerosene samples, sugesting high concentration levels of sulfur in crude oils. However, the obtained sulfur content levels are within the accepted standards in fuel oils, except for those of crude oil and kerosene samples. Therefore, the proposed m-SPE method followed by ICP-OES analysis has proven to be an alternative procedure for rapid and selective quantification of total sulfur in fuel samples.

Valorization and Upcycling of Acid Mine Drainage and Plastic Waste via the Preparation of Magnetic Sorbents for Adsorption of Emerging Contaminants.

Plastic waste poses a serious environmental risk, but it can be recycled to produce a variety of nanomaterials for water treatment. In this study, poly(ethylene terephthalate) (PET) waste and acid mine drainage were used in the preparation of magnetic mesoporous carbon (MMC) nanocomposites for the adsorptive removal of pharmaceuticals and personal care products (PPCPs) from water samples. The latter were then characterized using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET), and ζ potential. The results of Brunauer-Emmett-Teller isotherms revealed high specific surface areas of 404, 664, and 936 m2/g with corresponding pore sizes 2.51, 2.28, and 2.26 nm for MMC, MMAC-25%, and MMAC-50% adsorbents, respectively. Under optimized conditions, the equilibrium studies were best described by the Langmuir and Freundlich models and kinetics by the pseudo-second-order model. The maximum adsorption capacity for monolayer adsorption from the Langmuir model was 112, 102, and 106 mg/g for acetaminophen, caffeine, and carbamazepine, respectively. The composites could be reused for up to six cycles without losing their adsorption efficiency. Furthermore, prepared adsorbents were used to remove acetaminophen, caffeine, and carbamazepine from wastewater samples, and up to a 95% removal efficiency was attained.

From polyethylene waste bottles to UIO-66 (Zr) for preconcentration of steroid hormones from river water.

Metal-organic framework (UiO-66 (Zr) was synthesized using polyethylene terephthalate (PET) and used as an adsorbent for extraction and preconcentration of steroid hormones in river water. Polyethylene waste bottles were used as the source of polyethylene terephthalate (PET) ligands. The UIO-66(Zr), which the PET was made from recycled waste plastics, was used for the first time for the extraction and preconcentration of four different types of steroid hormones in river water samples. Various analytical characterization techniques were employed to characterize the synthesized material. The steroid hormones were detected and quantified using high-performance liquid chromatography coupled with diode array detector (HPLC-DAD). The results were further validated using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Experimental variables, such as sample pH, the mass of adsorbent and extraction time, were optimized using Box-Behnken design (BBD). The dispersive solid phase extraction method combined with HPLC-DAD, displayed good linearity (0.004-1000 µg/L) low limits of detections (LODs, 1.1-16 ng/L for ultrapure water and 2.6-5.3 ng/L for river water) and limits of quantification (LOQs, 3.7-5.3 ng/L for ultrapure water and 8.7-11.0 ng/L for river water samples) and acceptable extraction recoveries (86-101%). The intraday (n = 10) and interday (n = 5) precisions expressed in terms of relative standard deviations (%RSD) were all less than 5%. The steroid hormones were detected in most of the river water samples (Vaal River and Rietspruit River). The DSPE/HPLC method offered a promising approach for simultaneous extraction, preconcentration and determination of steroid hormones in water.

Hybrid porous material supported in a cellulose acetate polymeric membrane for the direct immersion thin-film microextraction of parabens in water.

A simple and sensitive direct immersion thin-film microextraction (DI-TFME) method based on MIL-101(Cr) modified with carbon nanofibers supported in cellulose acetate (CA-MIL-101(Cr)@CNFs) polymeric membrane was developed for the extraction and preconcentration of parabens in environmental water samples. A high-performance liquid chromatography-diode array detector (HPLC-DAD) was used for the determination and quantification of methylparaben (MP) and propylparaben (PP). The factors affecting the DI-TFME performance were investigated using central composite design (CCD). The linearity of the DI-TFME/HPLC-DAD method obtained under optimal conditions was 0.04-0.04-500 µg/L with a correlation coefficient (R2) greater than 0.99, respectively. The limits of detection (LOD) and quantification (LOQ) for methylparaben were 11 ng/L and 37 ng/L; for propylparaben, they were 13 ng/L and 43 ng/L, respectively. The enrichment factors were 93.7 and 123 for methylparaben and propylparaben. The intraday (repeatability) and interday (reproducibility) precisions expressed as relative standard deviations (%RSD) were less than 5%. Furthermore, the DI-TFME/HPLC-DAD method was validated using real water samples spiked with known concentrations of the analytes. The recoveries ranged from 91.5 to 99.8%, and intraday and interday trueness values were less than ±15%. The DI-TFME/HPLC-DAD approach was effectively used for the preconcentration and quantification of parabens in river water and wastewater samples.

Removal of methylene blue using MnO2@rGO nanocomposite from textile wastewater: Isotherms, kinetics and thermodynamics studies.

In this study, the adsorptive removal of methylene blue dye, which is commonly used in textile industries, was investigated using the MnO2@reduced graphene oxide (rGO) adsorbent. The sonication-assisted synthesis from rGO nanosheets and MnO2 nanoparticles resulted to the MnO2@rGO nanocomposite with improved physicochemical properties. The characterization results showed the improved surface area, porous structure and adsorption sites from the nitrogen adsorption-desorption studies, improved morphology from the Scanning Electron Microscope (SEM) and Transmission Electron Microscope (TEM) and the improved crystal structure from X-ray powder diffraction (XRD). The improved physicochemical properties on the MnO2@rGO nanocomposite played a significant role in enhancing the dye removal in textile wastewater. The equilibrium experimental data was best described by the Langmuir isotherm model with a maximum adsorption capacity of 156 mg g-1, suggesting a monolayer adsorption. The kinetic data best fitted the pseudo-second order kinetic model, suggesting a chemisorption adsorption process. The thermodynamic data (ΔG°, ΔH° and ΔS°) confirmed the feasibility, randomness and spontaneous nature of the adsorption process. The mechanism of adsorption involved the hydrogen bonding, π-π interactions and electrostatic interactions. The removal of methylene blue using MnO2@rGO nanocomposite in spiked textile wastewater yielded a 98-99% removal. The method demonstrated competitiveness when compared with literature reported results, paving way for further investigations towards industrial scale applications.

Combination of zeolitic imidazolate framework-67 and magnetic porous porphyrin organic polymer for preconcentration of neonicotinoid insecticides in river water.

A nanostructured material composed of zeolitic imidazolate framework-67 and magnetic porous porphyrin organic polymer (ZIF-67@MPPOP) was successfully synthesized and applied for the enrichment of neonicotinoid insecticides in river water. The analytes were detected and quantified using high performance liquid chromatography coupled with diode array detector (HPLC-DAD) and liquid chromatography mass spectrometry (LC-MS). Influential experimental parameters were optimized using response surface methodology based on Box Behnken design. The adsorption capacities were 69.46, 80.53, 85.39 and 90.0 mg g-1 for thiamethoxam, imidacloprid, acetamiprid and clothianidin, respectively. At optimal experimental conditions, low limit of detection (LOD), limit of quantification (LOQ) and linearity were 0.0091-0.04 µg L-1, 0.04-0.13 µg L-1 and (0.04-600 µg L-1), respectively. The relative standard deviation used to evaluate the reproducibility and repeatability of the method was less than 5%. Finally, the method was employed for determination of four neonicotinoid insecticides in river water.

Advanced Polymeric Nanocomposites for Water Treatment Applications: A Holistic Perspective.

Water pollution remains one of the greatest challenges in the modern era, and water treatment strategies have continually been improved to meet the increasing demand for safe water. In the last few decades, tremendous research has been carried out toward developing selective and efficient polymeric adsorbents and membranes. However, developing non-toxic, biocompatible, cost-effective, and efficient polymeric nanocomposites is still being explored. In polymer nanocomposites, nanofillers and/or nanoparticles are dispersed in polymeric matrices such as dendrimer, cellulose, resins, etc., to improve their mechanical, thermophysical, and physicochemical properties. Several techniques can be used to develop polymer nanocomposites, and the most prevalent methods include mixing, melt-mixing, in-situ polymerization, electrospinning, and selective laser sintering techniques. Emerging technologies for polymer nanocomposite development include selective laser sintering and microwave-assisted techniques, proffering solutions to aggregation challenges and other morphological defects. Available and emerging techniques aim to produce efficient, durable, and cost-effective polymer nanocomposites with uniform dispersion and minimal defects. Polymer nanocomposites are utilized as filtering membranes and adsorbents to remove chemical contaminants from aqueous media. This study covers the synthesis and usage of various polymeric nanocomposites in water treatment, as well as the major criteria that influence their performance, and highlights challenges and considerations for future research.

Synthesis of molecularly imprinted polymers for extraction of fluoroquinolones in environmental, food and biological samples.

In recent years, fluoroquinolones have been found present in important water resources and food sources which compromises the food quality and availability, thereby, causing risks to the consumer. Despite the recent advancement in the development of analytical instrumentation for routine monitoring of fluoroquinolones in water, food, and biological samples, sample pre-treatment is still a major bottleneck of the analytical methods. Therefore, fast, selective, sensitive, and cost-effective sample preparation methods prior to instrumental analysis for fluoroquinolones residues in environmental, food and biological samples are increasingly important. Solid-phase extraction using different adsorbents is one of the most widely used pre-concentration/clean-up techniques for analysis of fluoroquinolones. Molecularly imprinted polymers (MIPs) serve as excellent effective adsorbent materials for selective extraction, separation, clean-up and preconcentration of various pollutants in different complex matrices. Therefore, synthesis of MIPs remains crucial for their applications in sample preparation as this offers much-needed selectivity in the extraction of compounds in complex samples. In this study, the progress made in the synthesis of MIPs for fluoroquinolones and their applications in water, food and biological samples were reviewed. The present review discusses the selection of all the elements of molecular imprinting for fluoroquinolones, polymerization processes and molecular recognition mechanisms. In conclusion, the related challenges and gaps are given to offer ideas for future research focussing on MIPs for fluoroquinolones.

Magnetic Mesoporous Carbon/ß-Cyclodextrin-Chitosan Nanocomposite for Extraction and Preconcentration of Multi-Class Emerging Contaminant Residues in Environmental Samples.

This study reports the development of magnetic solid-phase extraction combined with high-performance liquid chromatography for the determination of ten trace amounts of emerging contaminants (fluoroquinolone antibiotics, parabens, anticonvulsants and ß-blockers) in water systems. Magnetic mesoporous carbon/ß-cyclodextrin-chitosan (MMPC/Cyc-Chit) was used as an adsorbent in dispersive magnetic solid-phase extraction (DMSPE). The magnetic solid-phase extraction method was optimized using central composite design. Under the optimum conditions, the limits of detection (LODs) ranged from 0.1 to 0.7 ng L-1, 0.5 to 1.1 ng L-1 and 0.2 to 0.8 ng L-1 for anticonvulsants and ß-blockers, fluoroquinolone and parabens, respectively. Relatively good dynamic linear ranges were obtained for all the investigated analytes. The repeatability (n = 7) and reproducibility (n = 5) were less than 5%, while the enrichment factors ranged between 90 and 150. The feasibility of the method in real samples was assessed by analysis of river water, tap water and wastewater samples. The recoveries for the investigated analytes in the real samples ranged from 93.5 to 98.8%, with %RSDs under 4%.

Magnetic Cellulose-Chitosan Nanocomposite for Simultaneous Removal of Emerging Contaminants: Adsorption Kinetics and Equilibrium Studies.

The presence of pharmaceuticals in water systems threatens both terrestrial and aquatic life across the globe. Some of such contaminants are ß-blockers and anticonvulsants, which have been constantly detected in different water systems. Various methodologies have been introduced for the removal of these emerging pollutants from different waters. Among them, adsorption using nanomaterials has proved to be an efficient and cost-effective process for the removal of pharmaceuticals from contaminated water. In this this study, a firsthand/time approach applying a recyclable magnetic cellulose-chitosan nanocomposite for effective simultaneous removal of two ß-blockers (atenolol (ATN)) and propranolol (PRP) and an anticonvulsant (carbamazepine (CBZ)) is reported. A detailed characterization of the eco-friendly, biocompatible cellulose-chitosan nanocomposite with magnetic properties was performed at various rates of synthesis using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), and Fourier transform infrared (FTIR) spectroscopy. A N2c adsorption-desorption test showed that the prepared nanocomposite is mesoporous, with a BET area of 112 m2 g-1. The BET isotherms results showed that the magnetic cellulose-chitosan nanocomposite has a pore size of 24.1 nm. The adsorption equilibrium of PRP and CBZ fitted with the Langmuir isotherm was consistent with the highest coefficient of determination (R2 = 0.9945) and (R2 = 0.9942), respectively, while the Sips model provided a better fit for ATN, with a coefficient of determination R2 = 0.9956. The adsorption rate was accompanied by a pseudo-second-order kinetics. Moreover, the swelling test showed that up to 100 percent swelling of the magnetic cellulose-chitosan nanocomposite was achieved.

MnO2@Reduced Graphene Oxide Nanocomposite-Based Electrochemical Sensor for the Simultaneous Determination of Trace Cd(II), Zn(II) and Cu(II) in Water Samples.

The rapid detection of trace metals is one of the most important aspect in achieving environmental monitoring and protection. Electrochemical sensors remain a key solution for rapid detection of heavy metals in environmental water matrices. This paper reports the fabrication of an electrochemical sensor obtained by the simultaneous electrodeposition of MnO2 nanoparticles and RGO nanosheets on the surface of a glassy carbon electrode. The successful electrodeposition was confirmed by the enhanced current response on the cyclic voltammograms. The XRD, HR-SEM/EDX, TEM, FTIR, and BET characterization confirmed the successful synthesis of MnO2 nanoparticles, RGO nanosheets, and MnO2@RGO nanocomposite. The electrochemical studies results revealed that MnO2@RGO@GCE nanocomposite considerably improved the current response on the detection of Zn(II), Cd(II) and Cu(II) ions in surface water. These remarkable improvements were due to the interaction between MnO2 nanomaterials and RGO nanosheets. Moreover, the modified sensor electrode portrayed high sensitivity, reproducibility, and stability on the simultaneous determination of Zn(II), Cd(II), and Cu(II) ions. The detection limits of (S/N = 3) ranged from 0.002-0.015 µg L-1 for the simultaneous detection of Zn(II), Cd(II), and Cu(II) ions. The results show that MnO2@RGO nanocomposite can be successfully used for the early detection of heavy metals with higher sensitivity in water sample analysis.

Magnetic Fe3O4@Mg/Al-layered double hydroxide adsorbent for preconcentration of trace metals in water matrices.

A magnetic Fe3O4@MgAl-layered double hydroxide (MLDH) nanocomposite was successfully synthesized and applied as an effective adsorbent for preconcentration of trace As(III), Cd(II), Cr(III), Co(II), Ni(II), and Pb(II) ions from complex matrices. The quantification of the analytes was achieved using the inductively coupled plasma optical emission spectrometry (ICP-OES) technique. The nanocomposite was then characterized using BET, FTIR, SEM, and EDS. Due to its high adsorption surface area, compared to traditional metal oxide-based adsorbents, MLDH nanocomposite exhibited high extraction efficiency. Several experimental parameters controlling the preconcentration of the trace metals were optimized using response surface methodology based on central composite design. Under optimum conditions, the linearity ranged from 0.1 to 500 µg L-1 and the correlation of coefficients (R2) were higher than 0.999. The limits of detection (LODs) and quantification (LOQs) were 0.11-0.22 µg L-1 and 0.35-0.73 µg L-1, respectively. The intra-day (n = 10) and inter-day precisions (n = 5 working days) expressed in the form of percent relative standard deviations (%RSDs) were below 5%. The proposed method was successfully applied for the analysis of the As(III), Cd(II), Cr(III), Co(II), Ni(II), and Pb(II) ions in different environmental water samples.

Magnetic Ion Imprinted Polymers (MIIPs) for Selective Extraction and Preconcentration of Sb(III) from Environmental Matrices.

Antimony(III) is a rare element whose chemical and toxicological properties bear a resemblance to those of arsenic. As a result, the presence of Sb(III) in water might have adverse effects on human health and aquatic life. However, Sb(III) exists at very ultra-trace levels which may be difficult for direct quantification. Therefore, there is a need to develop efficient and reliable selective extraction and preconcentration of Sb(III) in water systems. Herein, a selective extraction and preconcentration of trace Sb(III) from environmental samples was achieved using ultrasound assisted magnetic solid-phase extraction (UA-MSPE) based on magnetic Sb(III) ion imprinted polymer-Fe3O4@SiO2@CNFs nanocomposite as an adsorbent. The amount of antimony in samples was determined using inductively coupled plasma optical emission spectrometry (ICP-OES). The UA-MSPE conditions were investigated using fractional factorial design and response surface methodology based on central composite design. The Sb(III)-IIP sorbent displayed excellent selectivity towards Sb(III) as compared to NIIP adsorbent. Under optimised conditions, the enrichment factor, limit of detection (LOD) and limit of quantification (LOQ) of UA-MSPE/ICP-OES for Sb(III) were 71.3, 0.13 µg L-1 and 0.44 µg L-1, respectively. The intra-day and inter-day precision expressed as relative standard deviations (%RSDs, n = 10 and n = 5) were 2.4 and 4.7, respectively. The proposed analytical method was applied in the determination of trace Sb(III) in environmental samples. Furthermore, the accuracy of the method was evaluated using spiked recovery experiments and the percentage recoveries ranged from 95-98.3%.

Occurrence, Fate, Effects, and Risks of Dexamethasone: Ecological Implications Post-COVID-19.

The recent outbreak of respiratory syndrome-coronavirus-2 (SARS-CoV-2), which causes coronavirus disease (COVID-19), has led to the widespread use of therapeutics, including dexamethasone (DEXA). DEXA, a synthetic glucocorticoid, is among the widely administered drugs used to treat hospitalized COVID-19 patients. The global COVID-19 surge in infections, consequent increasing hospitalizations, and other DEXA applications have raised concerns on eminent adverse ecological implications to aquatic ecosystems. Here, we aim to summarize published studies on DEXA occurrence, fate, and effects on organisms in natural and engineered systems as, pre-COVID, the drug has been identified as an emerging environmental contaminant. The results demonstrated a significant reduction of DEXA in wastewater treatment plants, with a small portion, including its transformation products (TPs), being released into downstream waters. Fish and crustaceans are the most susceptible species to DEXA exposure in the parts-per-billion range, suggesting potential deleterious ecological effects. However, there are data deficits on the implications of DEXA to marine and estuarine systems and wildlife. To improve DEXA management, toxicological outcomes of DEXA and formed TPs should entail long-term studies from whole organisms to molecular effects in actual environmental matrices and at realistic exposure concentrations. This can aid in striking a fine balance of saving human lives and protecting ecological integrity.

Effect of the Zwitterion, p(MAO-DMPA), on the Internal Structure, Fouling Characteristics, and Dye Rejection Mechanism of PVDF Membranes.

The zwitterion poly-(maleic anhydride-alt-1-octadecene-3-(dimethylamino)-1-propylamine) (p(MAO-DMPA)) synthesized using a ring-opening reaction was used as a poly(vinylidene fluoride) (PVDF) membrane modifier/additive during phase inversion process. The zwitterion was characterized using proton nuclear magnetic resonance (1HNMR) and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR). Atomic force microscopy (AFM), field emission scanning electron microscope (SEM), FTIR, and contact angle measurements were taken for the membranes. The effect of the zwitterionization content on membrane performance indicators such as pure water flux, membrane fouling, and dye rejection was investigated. The morphology of the membranes showed that the increase in the zwitterion amount led to a general decrease in pore size with a concomitant increase in the number of membrane surface pores. The surface roughness was not particularly affected by the amount of the additive; however, the internal structure was greatly influenced, leading to varying rejection mechanisms for the larger dye molecule. On the other hand, the wettability of the membranes initially decreased with increasing content to a certain point and then increased as the membrane homogeneity changed at higher zwitterion percentages. Flux and fouling properties were enhanced through the addition of zwitterion compared to the pristine PVDF membrane. The high (>90%) rejection of anionic dye, Congo red, indicated that these membranes behaved as ultrafiltration (UF). In comparison, the cationic dye, rhodamine 6G, was only rejected to <70%, with rejection being predominantly electrostatic-based. This work shows that zwitterion addition imparted good membrane performance to PVDF membranes up to an optimum content whereby membrane homogeneity was compromised, leading to poor performance at its higher loading.