An alginate-based eutectogel impregnated with polyvinylpyrrolidone/benzoic acid deep eutectic solvent and magnetic carboxylated multiwalled carbon nanotubes: Evaluated as sorbent in green microextraction of pesticides.

This article presents the synthesis and application of a novel magnetic eutectogel constituting a polymeric deep eutectic solvent (PDES), carboxylated multiwall carbon nanotube (MWCNT-COOH), and super-dispersible/super-paramagnetic polyvinylpyrrolidone coated-Fe3O4 nanocrystals incorporated in alginate gel. Different methods were used for the characterization of novel polymeric based DES gel including FT-NMR, ATR-FTIR, and SEM were used. The novel DES eutectogel was used for the extraction of pesticides from honey. The modified eutectogel with PDES, MWCNT, and PDES-MWCNT showed 1.8-, 1.4-, and 2.5-fold enhancement in the sorption efficiency under green magnetic micro-solid-phase extraction (MSPE) method before GC-MS analysis. Important factors including the acidity of the samples, adsorption and desorption conditions, and the ionic strength of the preparation solution were investigated. The matrix effect, specificity, the quantification limits (0.023-1.023 µg kg-1), linear dynamic range (0.023-500 µg kg-1 with R2 of 0.9845-0.9986), relative standard deviations (<8.4%), were evaluated. In addition, the method was used to analyze 12 pesticides in four samples of honey. In the spiked concentration range of 0.1 to 10 µg kg-, the obtained recoveries were between 73.2 and 110.8% (RSD% = 8.1%, n = 3).

Removal of mercury ions from aqueous by functionalized LUS-1 with Bis [3-(triethoxysilyl) propyl] tetrasulfide as an effective nanocomposite using response surface methodology (RSM).

In this study, LUS-1, as a mesoporous silica material, was functionalized using sulfur-containing ligand (Bis [3-(triethoxysilyl) propyl] tetrasulfide, TESPT) and used for mercury removal from the aqueous solution. Different characterizations such as N2 adsorption-desorption (BET), TGA, XRD, FT-IR, and SEM were used to verify the nanocomposite synthesis. In addition, the effects of several independent parameters like pH, the contact time of reaction, and adsorbent dose on the removal efficiency of mercury from aqueous in a batch system were studied using response surface methodology (RSM). Based on the results and after both theoretical and experimental studies, the optimum conditions using the LUS-1-TESPT were contact time of reaction of 23.16 min, sorbent dose of 51.12 mg, and pH of 4.5. The kinetic and isotherm models for the adsorption process showed a maximum adsorption capacity of adsorbent which was 136.73 mg g-1 with 99% removal of Hg(II) via the Langmuir model. Meanwhile, the sorbent's reusability and efficiency verified that the sorbent could be used five times after recovery with 99% efficiency.

Removal of lead ions from wastewater using magnesium sulfide nanoparticles caged alginate microbeads.

In this study, an adsorbent made of alginate (Alg) caged magnesium sulfide nanoparticles (MgS) microbeads were used to treat lead ions (Pb2+ ions). The MgS nanoparticles were synthesized at low temperatures, and Alg@MgS hydrogel microbeads were made by the ion exchange process of the composite materials. The newly fabricated Alg@MgS was characterized by XRD, SEM, and FT-IR. The adsorption conditions were optimized for the maximum removal of Pb2+ ions by adjusting several physicochemical parameters, including pH, initial concentration of lead ions, Alg/MgS dosage, reaction temperature, equilibration time, and the presence of co-ions. This is accomplished by removing the maximum amount of Pb2+ ions. Moreover, the adsorbent utilized more than six times with a substantial amount (not less than 60%) of Pb2+ ions was eliminated. Considering the ability of sodium alginate (SA) for excellent metal chelation and controlled nanosized pore structure, the adsorption equilibrium of Alg@MgS can be reached in 60 min, and the highest adsorption capacity for Pb2+ was 84.7 mg/g. The sorption mechanism was explored by employing several isotherms. It was found that the Freundlich model fits the adsorption process quite accurately. The pseudo-second-order model adequately described the adsorption kinetics.

Sulfide-Doped Magnetic Carbon Nanotubes Developed as Adsorbent for Uptake of Tetracycline and Cefixime from Wastewater.

In this study, a magnetic solid-phase extraction method was developed based on multi-wall carbon nanotubes decorated by magnetic nanoparticles (Fe3O4) and cadmium sulfide nanoparticles (Fe3O4@MWCNT-CdS) for trace extraction of cefixime and tetracycline antibiotics from urine and drug company wastewater. The adsorbent features were characterized by Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FESEM), and energy dispersive X-ray analysis (EDX). Various effective parameters on the sorption and desorption cycle, such as sorption time, the mass of adsorbent, pH, salt addition, and material ratio, were investigated and optimized. The data were evaluated using isotherm models, and experimental data were well-fitted to both Langmuir (R2 = 0.975) and Freundlich (R2 = 0.985) models. Moreover, kinetic of reaction was agreement with pseudo-second-order (R2 = 0.999) as compared pseudo-first-order (R2 = 0.760). The maximum adsorption capacity for tetracycline and cefixime was achieved at 116.27 and 105.26 mg·g-1, respectively. Hence, the prepared adsorbent can be used as an alternative material for enhanced determination of pharmaceutical substances in biological fluids.

Nano-Size Biomass Derived from Pomegranate Peel for Enhanced Removal of Cefixime Antibiotic from Aqueous Media: Kinetic, Equilibrium and Thermodynamic Study.

Nano-sized activated carbon was prepared from pomegranate peel (PG-AC) via NaOH chemical activation and was fully characterized using BET, FT-IR, FE-SEM, EDX, and XRD. The newly synthesized PG-AC was used for cefixime removal from the aqueous phase. The effective parameters on the adsorption process, including solution pH (2-11), salt effect (0-10%), adsorbent dosage (5-50 mg), contact time (5-300 min), and temperature (25-55 °C) were examined. The experimental adsorption equilibrium was in close agreement with the type IV isotherm model set by the International Union of Pure and Applied Chemistry (IUPAC). The adsorption process was evaluated with isotherm, kinetic, and thermodynamic models and it is were well fitted to the Freundlich isotherm (R2 = 0.992) and pseudo-second-order model (R2 = 0.999). The Langmuir isotherm provided a maximum adsorption capacity of 181.81 mg g-1 for cefixime uptake onto PG-AC after 60 min at pH 4. Hence, the isotherm, kinetic and thermodynamic models were indicated for the multilayer sorption followed by the exothermic physical adsorption mechanism.

Efficient removal of arsenic(III) from aqueous media using magnetic polyaniline-doped strontium-titanium nanocomposite.

In this study, a novel nanocomposite adsorbent based on magnetic polyaniline and strontium-titanium (MP-SrTiO3) nanoparticles was synthesized via a simple and low-cost polymerization method for efficiently removing of arsenic(III) ions from aqueous samples. The chemical structure, surface properties, and morphology of the prepared adsorbent were studied using Fourier transform infrared spectroscopy (FTIR), energy-dispersive X-ray spectroscopy (EDX), and scanning electron microscopy (SEM). The main effective parameters on the removal efficiency, such as pH, adsorbent dosage, salt, and contact time, were studied and optimized. The validity of the proposed method was checked by adsorption isotherm and kinetics models. Consequently, the adsorption kinetics corresponded to the first order (R2 > 0.99), and the experimental equilibrium fitted the Langmuir model with a maximum monolayer adsorption capacity of 67.11 mg/g (R2 > 0.99) for arsenic(III) ions. Corresponding to thermodynamic Vant's Hof model (ΔG° (kJ/mol), ΔH° (kJ/mol), and ΔS° (kJ/mol K) - 8.19, - 60.61, and - 0.17, respectively), the mechanism and adsorption nature were investigated with that suggested exothermic and physisorption mechanism.

Modified Mesoporous Silica (SBA-15) with Trithiane as a new effective adsorbent for mercury ions removal from aqueous environment.

BACKGROUND: Removal of mercury from aqueous environment has been highly regarded in recent years and different methods have been tested for this purpose. One of the most effective ways for mercury ions (Hg(+2)) removal is the use of modified nano porous compounds. Hence, in this work a new physical modification of mesoporous silica (SBA-15) with 1, 3, 5 (Trithiane) as modifier ligand and its application for the removal of Hg(+2) from aqueous environment has been investigated. SBA-15 and Trithiane were synthesized and the presence of ligand in the silica framework was demonstrated by FTIR spectrum. The amounts of Hg(+2) in the samples were determined by cold vapor generation high resolution continuum source atomic absorption spectroscopy. Also, the effects of pH, stirring time and weight of modified SBA-15 as three major parameters for effective adsorption of Hg(+2) were studied. RESULTS: The important parameter for the modification of the adsorbent was Modification ratio between ligand and adsorbent in solution which was 1.5. The results showed that the best Hg(+2) removal condition was achieved at pH = 5.0, stirring time 15 min and 15.0 mg of modified adsorbent. Moreover, the maximum percentage removal of Hg(+2) and the capacity of adsorbent were 85% and 10.6 mg of Hg(+2)/g modified SBA-15, respectively. CONCLUSIONS: To sum up, the present investigation introduced a new modified nano porous compound as an efficient adsorbent for removal of Hg(+2) from aqueous environment.