Nanosorbent based on coprecipitation of ZnO in goethite for competitive sorption of Cd(II)-Pb(II) and Cd(II)-Pb(II)-Ni(II) systems.

Amongst the various water pollutants, heavy metal ions require special attention because of their toxic nature and effects on humans and the environment. Preserving natural resources will have positive impacts on living conditions by reducing diseases and water treatment by nanotechnology is effective in solving this problem owing to the properties of nanomaterials. In this study, a goethite nanoparticle was prepared by hydrothermal method, while ZnO/goethite nanocomposite by co-precipitation was developed. The nanoparticles were characterized using Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Transform Electron Microscopy (TEM), Thermogravimetric Differential Thermal Analysis (TGA-DTA), Dynamic Light Scattering (DLS), and Breunner-Emmet-Teller (BET) surface area analysis. The adsorption of Cd(II)-Pb(II) and Cd(II)-Pb(II)-Ni(II) ions systems on ZnO/goethite nanocomposite was investigated in a batch mode. The findings of the study showed that nanoparticles ZnO/goethite composite were mixed of spherical and rod-like shapes. The BET results revealed average particle sizes of 41.11 nm for nanoparticles for ZnO/goethite while TGA/DTA confirmed the stability of the adsorbents. The optimum adsorption capacities of the nanocomposite for Pb(II), Cd(II), and Ni(II) ions from the Pb-Cd-Ni ternary system were 415.5, 195.3, and 87.13 mg g-1, respectively. The adsorption isotherm data fitted well with the Langmuir isotherm model. The study concluded that the nanoparticle adsorbents are efficient for the remediation of toxic pollutants and are, therefore, recommended for wastewater treatment.

Comparative evaluation of liquid-liquid extraction and nanosorbent extraction for HPLC-PDA analysis of cabazitaxel from rat plasma.

A precise, sensitive, accurate, and validated reverse-phase high-performance liquid chromatography (RP-HPLC) method with a bioanalytical approach was utilized to analyze Cabazitaxel (CBZ) in rat plasma. Comparative research on extraction recoveries was performed between traditional liquid-liquid extraction (LLE) and synthesized graphene oxide (GO) based magnetic solid phase extraction (GO@MSPE). The superparamagnetic hybrid nanosorbent was synthesized using the combination of iron oxide and GO and subsequently applied for extraction and bioanalytical quantification of CBZ from plasma by (HPLC-PDA) analysis. Fourier- transform infrared spectroscopy (FT-IR), particle size, scanning electron microscopy (SEM), and x-ray diffraction (XRD) analysis were employed in the characterization of synthesized GO@MSPE nanosorbent. The investigation was accomplished using a shim pack C18 column (150 mm×4.6 mm, 5 µm) with a binary gradient mobile phase consisting of formic acid: acetonitrile: water (0.1:75:25, v/v/v) at a 0.8 mL/min flow rate, and a λmax of 229 nm. The limits of detection (LOD) and quantitation (LOQ) have been determined to be 50 and 100 ng/mL for both LLE and SPE techniques. The linearity range of the approach encompassed from 100 to 5000 ng/mL and was found to be linear (coefficient of determination > 0.99) for CBZ. The proposed method showed extraction recovery of 76.8-88.4% for the synthesized GO@MSPE and 69.3-77.4% for LLE, suggesting that the proposed bioanalytical approach was robust and qualified for all validation parameters within the acceptable criteria. Furthermore, the developed hybrid GO@MSPE nanosorbent with the help of the proposed RP-HPLC method, showed a significant potential for the extraction of CBZ in bioanalysis.

Magnetic silica nanoparticles adorned with a metal-organic framework; a novel nanosorbent for elimination of aqueous Pb ions contaminant.

The annual growth of water pollution resulting from the uncontrolled entry of heavy metals, like Pb2+ ions, is one of the most critical global concerns due to its direct and indirect effects on human life. The absorption of this component by the body could affect the nervous system via oxidative stress production or disturbing cellular biological mechanism. So, it is important to find an effective method for purifying the existing waters. This study aims to fabricate and compare the effect of two new nano-adsorbents (Fe3O4@ZIF-8 and Fe3O4@SiO2@ZIF-8) on removing Pb2+ ions from the aqueous solution. Accordingly, iron oxide nanoparticles were synthesized via co-precipitation method at first and then coated with a silica shell through the sol-gel method. Both nanoparticles were coated with a layer of metal-organic framework (MOF), ZIF-8, and analyzed with different physicochemical tests. In the following parts, the Pb2+ ion removal capability of the nano-adsorbents was evaluated in the presence of different parameters, including nanosorbent concentrations, contact time, pH, and pollutant concentrations. Results confirmed preparation of nanoparticles with a mean size of about 110 ± 10 nm and 80 ± 10 nm for Fe3O4@ZIF-8 and Fe3O4@SiO2@ZIF-8, respectively. Both nanoparticles showed the highest amount of pollutants removal (near 90% for both nanoparticles) at pH = 6 within 15 min of contact in the presence of 100 ppm Pb2+ ions. Besides, in the case of real samples, with a concentration of about 150 ppm of Pb2+ ions, they showed maximum adsorption of about 93.61% and 99.2% for Fe3O4@ZIF-8 and Fe3O4@SiO2@ZIF-8, respectively. The presence of iron oxide nanoparticles in the structure of this adsorbent makes it easy to separate them in a user-friendly method. A brief comparison between these nanosorbents indicates that Fe3O4@SiO2@ZIF-8 nanoparticles have better performance due to their higher porosity and surface area ratio and so it could be used as a cost-effective ideal nanosorbent candidate for easy removal of heavy metals from water.

Mussel - Inspired biosorbent combined with graphene oxide for removal of organic pollutants from aqueous solutions.

In this work, we develop a mussel-inspired biosorbent combined with graphene oxide for removal of organic dyes in water sources. The composite was prepared via self-polymerization of dopamine in weak alkaline solution containing graphene oxide at ambient condition. Morphological and structural studies revealed that polydopamine has gradually grown to cover the surface of graphene oxide flakes, partially reduced these flakes, and somehow form many grains (size around 20 nm) on the flakes instead of making very large aggregates as usual. The mass ratio between two components of the composite was also investigated to find the optimal one which provides enough surface area (20 m2.g-1) and maintain adhesive sites in order to ensure high-efficiency removal of organic molecules. The adsorption kinetics and isotherms of as-prepared adsorbent towards methylene blue were found to fit well with pseudo-first order kinetics model and Langmuir isotherm. The maximum adsorption capacity (qm) and Langmuir constant (kL) were estimated to be 270 mg.g-1 and 0.49 L. mg-1. The as-prepared bio-sorbent is very promising for remediation of water sources contaminated with cationic organic molecules and heavy metal ions.

Chitosan Nanoparticles as Potential Nano-Sorbent for Removal of Toxic Environmental Pollutants.

Adsorption is the most widely used technique for advanced wastewater treatment. The preparation and application of natural renewable and environmentally friendly materials makes this process easier and more profitable. Chitosan is often used as an effective biomaterial in the adsorption world because of its numerous functional applications. Chitosan is one of the most suitable and functionally flexible adsorbents because it contains hydroxyl (-OH) and amine (-NH2) groups. The adsorption capacity and selectivity of chitosan can be further improved by introducing additional functions into its basic structure. Owing to its unique surface properties and adsorption ability of chitosan, the development and application of chitosan nanomaterials has gained significant attention. Here, recent research on chitosan nanoparticles is critically reviewed by comparing various methods for their synthesis with particular emphasis on the role of experimental conditions, limitations, and applications in water and wastewater treatment. The recovery of pollutants using magnetic nanoparticles is an important treatment process that has contributed to additional development and sustainable growth. The application of such nanoparticles in the recovery metals, which demonstrates a "close loop technology" in the current scenarios, is also presented in this review.

Effect of graphene oxide on the uptake, translocation and toxicity of metal mixture to Lepidium sativum L. plants: Mitigation of metal phytotoxicity due to nanosorption.

Due to its unique structure and exceptional properties, graphene oxide (GO) is increasingly used in various fields of industry and therefore is inevitably released into the environment, where it interacts with different contaminants. However, the information relating to the ability of GO to affect the toxicity of contaminants is still limited. Therefore, the aim of our study was to synthesize GO, to examine the phytotoxicity of different concentrations of GO and its co-exposure with the metal mixture using garden cress (Lepidium sativum L.) as a test organism and to evaluate the potential of GO to affect toxicity of metals and their uptake by plants. The metal mixture (MIX) containing Ni (II), Zn (II), Cr (III) and Cu (II) was prepared in accordance with the maximum-permissible-concentrations (MPC) accepted for the inland waters in the EU. Additionally, the capacity of GO to adsorb metals was studied in specific conditions of the phytotoxicity test and assessed using adsorption isotherms. Our data indicate that in most cases the tested concentrations of MIX, GO and MIX + GO did not affect seed germination, root growth and biomass of roots and seedlings, however, they were found to alter photosynthesis processes, enhance production of carotenoids and H2O2 as well as to activate lipid peroxidation. Additionally, our study revealed that GO affects the accumulation of tested metals in roots and shoots of the MIX-exposed L. sativum. This is due to the capacity of GO to adsorb metals from the growth medium. Therefore, low concentrations of GO can be used for water decontamination.

Evaluation of Heavy Metal Removal of Nanoparticles Based Adsorbent Using Danio rerio as Model.

Nanoparticles are potential candidates for wastewater treatment especially for the removal of heavy metals due to their strong affinity. Many biopolymers are used as adsorbents and encapsulation of nanoparticle onto them can increase their efficiency. In this study, SPIONs, alginate, and SPIONs incorporated on alginate beads have been synthesized and characterized both microscopically and spectroscopically. These were then used for the removal of chromium metal and the percentage of removal was evaluated using a batch adsorption study. The percent removal of chromium using SPIONs, alginate and alginate-SPIONs beads were recorded to be 93%, 91% and 94%, respectively. The adsorption of chromium using SPIONs and alginate-SPIONs beads followed the Tempkin isotherm, whereas adsorption of chromium metal by alginate beads was found to be homogeneous in nature and followed the Langmuir isotherm with an R2 value of 0.9784. An in-vivo study using Danio rerio as a model organism was done to examine the toxicity and the removal efficiency of the samples. It was observed that chromium water treated with alginate-SPIONs beads, which were removed after water treatment showed less damage to the fishes when compared to SPIONs and alginate beads treated with chromium water where the SPIONs and alginate beads were not removed after the treatment period.

Microwave-assisted synthesis of MnO2 nanosorbent for adsorptive removal of Cs(I) and Sr(II) from water solutions.

In this study, a flower-like porous δ-MnO2 nanostructure was synthesized by a microwave-assisted hydrothermal process for adsorptive removal of strontium (Sr(II)) and cesium (Cs(I)) from wastewater. The prepared δ-MnO2 nanosorbent exhibited superior affinity for Sr(II) over Cs(I) in the single-solute system, with partition coefficient (PC) values of 10.2 and 2.3 L/g, respectively, at pH 6.0. In the two-solute system, the flower-like δ-MnO2 also adsorbed Sr(II) (PC = 3.81 L/g) more selectively than Cs(I) (PC 1.15 L/g). Further, their adsorption capacities decreased by 12 and 16%, respectively, relative to the single-solute system. In contrast, adsorption of the ions onto δ-MnO2 was affected less sensitively in dual than in single system when changes occurred in environmental variables such as pH (2-8) and ionic strength (1-100 mM). Adsorption kinetics, thermodynamics, and isotherm studies demonstrated the pivotal role of the monolayer surface active sites of endothermic δ-MnO2 (e.g., a complexation interaction with Mn-OH). Furthermore, the δ-MnO2 nanosorbent exhibited good regenerability, retaining more than 80% of its adsorption capacity when tested over four reuse cycles. The overall results of this study are expected to help establish strategies to effectively remove metal contaminants from wastewater using a green and low-cost hierarchical nanosorbent.

Hexavalent chromium removal from aqueous solutions using biogenic iron nanoparticles: Kinetics and equilibrium study.

Green mediated biosynthesis of iron oxide nanoparticles utilising Rosa indica flower petal extracts (RIFP-FeONPs) was used in this investigation. The RIFP-FeONPs were evaluated by the UV-Visible Spectroscopy, FTIR, SEM, EDX, XRD, Zeta potentials, and DLS, and been engaged than for the elimination of Cr (VI) from the contaminated environments. At 269 nm, the RIFP-FeONPs surface plasmon vibration bands were observed, which attributed to the Fe3+. XRD patterns of RIFP-FeONPs depicted the intense diffraction peak of face-centered cubic (fcc) iron at a 2θ value of 45.33° from the (311) lattice plane indisputably revealed that the particles are constituted of pure iron. The fabricated nanomaterials are spherical and polydisperse with a diameter of 70-120 nm, and various agglomeration clusters are attributable to intermolecular interaction. Zeta potential measurement and particle size distribution of RIFP-FeONPs showed a mean average size of 115.5 ± 29 nm and a polydispersity index (PDI) of 0.420. The study aims to analyse the appropriateness of RIFP-FeONPs for removing hexavalent chromium from the aqueous environment and the application of adsorption isotherm and statistical models in the experiment. The sorption of Cr (VI) on RIFP-FeONPs was observed to fit well with the isothermal models (R2 = 0.98). The linear correlation between processing parameters and time demonstrated that the adsorption efficiency of Cr (VI) well correlated with the pseudo-first order kinetic model and isothermal adsorption with the Langmuir and Freundlich isothermal models, so that the RIFP-FeONPs could be a prospective nanosorbent for hexavalent chromium removal from industrial waste.

Decontamination of fenitrothion from aqueous solutions using rGO/MoS2/Fe3O4 magnetic nanosorbent: synthesis, characterization and removal application.

In the present work, rGO/MoS2/Fe3O4 nanocomposite was synthesized and after confirmation of the structure by FTIR, XRD, and FESEM techniques, its performance as nanosorbent was investigated for the removal of fenitrothion pesticide from the aqueous media. The parameters affecting the removal process including agitation time, pH of the reaction medium, adsorbent content, initial analyte concentration as well as desorption parameters were investigated and optimized. Under optimum conditions (pH = 7, adsorbent amount: 30 mg, adsorption and desorption time: 5 min, eluent type and volume: 0.01 M ethanol-acetic acid and 4 mL), the synthesized adsorbent was able to remove fenitrothion pesticide up to 98% with an adsorption capacity of 33.4 mg/g. By investigation of the line equation and the correlation coefficient value, it was found that the adsorption process, in this study, follows the Langmuir model.

Highly Efficient Methylene Blue Dye Removal by Nickel Molybdate Nanosorbent.

Removing methylene blue (MB) dye from aqueous solutions was examined by the use of nickel molybdate (α-NiMoO4) as an adsorbent produced by an uncomplicated, rapid, and cost-effective method. Different results were produced by varying different parameters such as the pH, the adsorbent dose, the temperature, the contact time, and the initial dye concentration. Adsorbent dose and pH had a major removal effect on MB. Interestingly, a lower amount of adsorbent dose caused greater MB removal. The amount of removal gained was efficient and reached a 99% level with an initial methylene blue solution concentration of ≤160 ppm at pH 11. The kinetic studies indicated that the pseudo-second-order kinetic model relates very well with that of the obtained experimental results. The thermodynamic studies showed that removing the MB dye was favorable, spontaneous, and endothermic. Impressively, the highest quantity of removal amount of MB dye was 16,863 mg/g, as shown by the Langmuir model. The thermal regeneration tests revealed that the efficiency of removing MB (11,608 mg/g) was retained following three continuous rounds of recycled adsorbents. Adsorption of MB onto α-NiMoO4 nanoparticles and its regeneration were confirmed by Fourier transform infrared spectroscopy (FTIR) analysis and scanning electron microscopy (SEM) analysis. The results indicated that α-NiMoO4 nanosorbent is an outstanding and strong candidate that can be used for removing the maximum capacity of MB dye in wastewater.

Vortex-assisted Dispersive Solid-phase Extraction Using Schiff-base Ligand Anchored Nanomagnetic Iron Oxide for Preconcentration of Phthalate Esters and Determination by Gas Chromatography and Flame Ionization Detector.

Phthalate esters are synthetic chemicals that are widely used in plastic industries as plasticizer. They are harmful to humans and could be carcinogenic. In this research, a new nanosorbent was prepared via a Schiff-base reaction between p-dimethylaminobenzaldehyde and Fe3O4@SiO2-NH2 nanoparticles. A characterization of the sorbent was performed by Fourier-transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, and energy-dispersive spectroscopy. A modified nanosorbent has a core shell structure, and shows a great tendency towards the sorption of phthalate esters. Hence, it was utilized for the dispersive solid-phase extraction of six phthalate esters and determination by gas chromatography-flame ionization detection. Several variables, such as the pH, sorbent amount, salt effects, extraction and desorption time, extraction solvent type and volume, were investigated to establish the optimal conditions. Calibration graphs were linear in the range of 1.0 - 150.0 µg L-1 for dimethyl phthalate, bis-(2-ethylhexyl) phthalate, di-n-octyl phthalate and 0.1 - 200.0 µg L-1 for diethyl phthalate, di-n-butyl phthalate and butyl benzyl phthalate, respectively. The obtained limits of detections (S/N = 3) were in the range of 0.02 - 0.31 µg L-1. Application of the method for the enrichment and determination of phthalate esters in mineral water, natural low fat yogurt and sodium chloride infusion (0.9%, w/v) was investigated.

Iron Molybdate Fe2(MoO4)3 Nanoparticles: Efficient Sorbent for Methylene Blue Dye Removal from Aqueous Solutions.

The present study investigated iron molybdate (Fe2(MoO4)3), synthesized via a simple method, as a nanosorbent for methylene blue (MB) dye removal from aqueous solutions. Investigations of the effects of several parameters like contact time, adsorbent dose, initial dye concentration, temperature and pH were carried out. The results showed that MB removal was affected, significantly, by adsorbent dose and pH. Interestingly, lower values of adsorbent dose resulted in the removal of higher amounts of MB. At the optimum pH, the removal efficiency of 99% was gained with an initial MB concentration of ≤60 ppm. The kinetic study specified an excellent correlation of the experimental results with the pseudo-second-order kinetics model. Thermodynamic studies proved a spontaneous, favorable and endothermic removal. The maximum amount of removal capacity of MB dye was 6173 mg/g, which was determined from the Langmuir model. The removal efficiency was shown to be retained after three cycles of reuse, as proven by thermal regeneration tests. The presence and adsorption of the dye onto the Fe2(MoO4)3 nanoparticle surface, as well as the regeneration of the latter, was ascertained by scanning electron microscopy (SEM) and Fourier-transform infrared spectroscopy (FTIR). These findings are indicative that the investigated nanosorbent is an excellent candidate for the removal of MB in wastewater.

Electrodeposition of poly-ethylenedioxythiophene-graphene oxide nanocomposite in a stainless steel tube for solid-phase microextraction of letrozole in plasma samples.

Coated stainless steel was used as an in-tube solid-phase microextraction for the extraction of letrozole from plasma samples. The coating process on the inner surface of the stainless steel was conducted by a simple electrodeposition process. The coated composite was prepared from 3,4-ethylenedioxythiophene and graphene oxide. In this composite, graphene oxide acts as an anion dopant and sorbent. The coated nanostructured polymer was characterized using different techniques. The operational factors affecting the extraction process, including pH, adsorption, and desorption time, the recycling flow rate of the sample solution, sample volume, desorption solvent type and its volume, and ionic strength were optimized to achieve the best extraction efficiency of the analyte. The total extraction time including adsorption and desorption steps was about 15.0 min. The developed method demonstrated a linear range of 5.0-1500.0 µg/L with a limit of detection of 1.0 µg/L. The repeatability of the developed extraction approach in terms of intraday, interday, and fiber to fiber was attained in the range of 4.9-8.3%. After finding the optimal conditions, the potential of the described approach for letrozole quantitation was investigated in plasma samples, and satisfactory results were obtained.

In-tube stir bar sorptive extraction based on 3-aminopropyl triethoxysilane surface-modified Ce-doped ZnAl layered double hydroxide thin film for determination of nonsteroidal anti-inflammatory drugs in saliva samples.

A thin-film based on 3-aminopropyl triethoxysilane surface-modified Ce-doped zinc-aluminum layered double hydroxide was synthesized on the inner surface of an aluminum tube. It has been applied to in-tube stir bar sorptive extraction of nonsteroidal anti-inflammatory drugs in saliva samples followed by high-performance liquid chromatography. The sorbent was characterized by scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, and elemental mapping. The extraction parameters including sample pH (4.2), extraction time (10 min), stirring speed (800 rpm), type of eluent (acidified tetrahydrofuran), eluent volume (100 µL), and desorption time (6 min) were thoroughly optimized. Under the optimum conditions, limits of detection were found to be less than 5.0 ng mL-1. Calibration plots were linear within the range 10-1000 ng mL-1 (R2 > 0.9982). Absolute recoveries were calculated in the range 63.5 to 72.4%. The repeatability (intra- and inter-day precision) and reproducibility (tube-to-tube precision) at concentrations of 50, 250, and 500 ng mL-1 were less than 7.6% and 9.4%, respectively. The method accuracy based on the relative error was calculated at these concentrations and ranged from - 4.9 to - 9.3% for intra-day relative error (%) and - 6.8 to - 11% for inter-day relative error (%). Finally, the method applicability was examined for the determination of nonsteroidal anti-inflammatory drugs in saliva samples, and good relative recoveries were obtained within the range 86.5 to 95.2%. As a result, the introduced method can be applied as a suitable alternative to measuring nonsteroidal anti-inflammatory drugs in biological fluids. Graphical abstract A surface-modified Ce-doped ZnAl LDH thin film was synthesized on the inner surface of an Al tube and applied for in-tube stir bar sorptive extraction of NSAIDs in saliva.

Combining graphite with hollow-fiber liquid-phase microextraction for improving the extraction efficiency of relatively polar organic compounds.

In this study, we have developed a simple and effective hybrid extraction method based on the incorporation of raw carbon nanosorbents and octanol in the pores of a hollow-fiber membrane for improving the extraction efficiency of relatively polar organic compounds. Trihalomethanes (THMs) were used as model analytes. Three types of carbon nanosorbents (graphite, graphene, and multi-walled carbon nanotubes) were studied. The carbon sorbent incorporating membrane was used in a two-phase mode liquid-phase microextraction, with 1-octanol as the acceptor solution. Using a graphite-reinforced hollow-fiber membrane and an extraction time of 10 min, enrichment factors of 40-71 were obtained for trichloromethane, bromodichloromethane, bromoform, and chlorodibromomethane. Linear working ranges of 0.2-100 µg L-1 and limits of detection ranging from 0.01 µg L-1 (for CHCl2Br and CHClBr2) to 0.1 µg L-1 (for CHCl3) were achieved. The minimum detectable concentrations were far below the maximum concentration levels (60-200 µg L-1) set by the WHO for drinking water. The carbon-sorbent-reinforced hollow-fiber liquid-phase microextraction afforded higher extraction efficiency and shorter extraction time compared with conventional hollow-fiber liquid-phase microextraction. Finally, the method was applied to the analysis of real water samples, such as drinking water, tap water, and swimming pool water samples.

Polyacrylonitrile/MIL-53(Fe) electrospun nanofiber for pipette-tip micro solid phase extraction of nitrazepam and oxazepam followed by HPLC analysis.

Nanofibers were prepared from a nanocomposite consisting of polyacrylonitrile and a metal-organic framework of type MIL-53(Fe) by electrospinning. They are shown to be a viable sorbent for pipette-tip solid-phase extraction for the extraction of the benzodiazepine drugs nitrazepam and oxazepam. The nanofibers were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy and X-ray diffraction. The effects of sample pH value and volume, composition, and amount of electrospun nanofibers, the number of adsorption cycles and the type and volume of the eluent were optimized. Following extraction the drugs were quantified by HPLC. Under the optimized conditions, response is linear for both drugs in the 5.0-1000 ng mL-1 concentration range. The limits of detection for oxazepam and nitrazepam are 1.5 and 2.5 ng mL-1, respectively, and the relative standard deviations at the levels of 50, 100 and 250 ng mL-1 (for n = 3) are ≤7.6%. The method was successfully applied for determination of drugs in spiked wastewater and biological fluids. Graphical abstractSchematic representation of polyacrylonitrile/MIL-53(Fe) composite nanofiber synthesis by electrospinning, and the use of them as the sorbent in pipette-tip microsolid-phase extraction (PT-µSPE) for the preconcentration of Nitrazepam and Oxazepam before HPLC-DAD analysis.

Alginate-based magnetic nanosorbent immobilized with aptamer for selective and high adsorption of Hg2+ in water samples.

Alginate-coated magnetic nanocluster (MNC) immobilized with Hg2+-specific aptamer was synthesized to obtain the nanosorbent with high adsorption capacity and high selectivity for trace analysis of inorganic mercury (Hg2+) in water samples. Magnetite nanoparticle was first synthesized by a co-precipitation of iron precursors in the presence of alginate to obtain alginate-coated MNC, followed by immobilization with avidin. Hg2+-Specific DNA aptamer labeled with biotin was then conjugated on the MNC surface via specific avidin-biotin interaction to form aptamer-immobilized MNC. Coating the MNC with alginate can improve its water dispersibility and also increase its adsorption capacity toward Hg2+ (350 mg/g). It exhibited high selectivity through thymine-Hg2+-thymine (T-Hg2+-T) interaction with high tolerance to other foreign ions. This nanosorbent showed linearity over the Hg2+ concentration range of 0.2-10 µg/L with a correlation coefficient of 0.9977, limit of detection of 0.46 µg/L, and enrichment factor of 13. Moreover, it also showed a potential for detection of Hg2+ in drinking and tap water samples with satisfactory recoveries.

Fabrication of novel amine-functionalized magnetic silica nanoparticles for toxic metals: kinetic and isotherm modeling.

In this research, an amine-functionalized magnetic silica nanosorbent was prepared using the co-precipitation technique, and this nanosorbent can be effortlessly detached using an external magnetic field. FTIR and SEM analyses identified that the nanosorbent holds extraordinary adsorption characteristics for toxic metals' (copper, cadmium, zinc, and nickel) removal. The adsorption-affecting parameters were optimized, and the thermodynamic studies assessed that the adsorption process seemed to be spontaneous, feasible, and exothermic. The pseudo-first-order and Freundlich models perfectly fit the kinetic and equilibrium data, respectively. Langmuir monolayer capacity of the nanosorbent was analyzed using nonlinear evaluation methods such as 419.9 mg/g for copper, 321.9 mg/g for nickel, 217.3 mg/g for cadmium, and 137.6 mg/g for zinc. The used adsorbent was simply rejuvenated using the 0.2 N HCl solution subsequently with intense agitation. The result of the present research confirms that the produced nanosorbent can be effectively utilized for industrial wastewater management.

Enhanced adsorption of Cr(VI), Ni(II) ions from aqueous solution using modified Eichhornia crassipes and Lemna minor.

The environment is seriously affected by the release of hazardous heavy metals from the industries. The transformation of aquatic weeds into valuable nanosorbent has been considered as effective and efficient material in the wastewater treatment process. The aim of the study is to analyze the potential of nano-EC and nano-LM for the removal of chromium(VI) and nickel(II) ions. The characteristics of nanosorbent were analyzed using Fourier transform infrared spectroscopy (FTIR), Brunauer Emmett-Teller analysis (BET), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX), and thermo gravimetric analysis (TGA), respectively. Adsorptive performance of nanosorbent was studied with respect to pH, contact time, nano adsorbent dosage, and metal ion concentration. The maximum monolayer adsorption capacity of Cr(VI) and Ni(II) with respect to nano-EC was found to be 79.04 mgg-1 and 85.09 mgg-1, respectively. Adsorption isotherm and kinetic studies were performed and it was reported that adsorption isotherm follows Langmuir model with regression coefficient R2 > 0.9 for nano-EC and nano-LM respectively. The pseudo-second order model was found to fit well with experimental data. Experimental results suggested that nano-EC can be considered as a suitable nanosorbent for the removal of Cr(VI) and Ni(II) ions from effluents.