Hexavalent chromium ion removal from wastewater using novel nanocomposite based on the impregnation of zero-valent iron nanoparticles into polyurethane foam.

In this study, we developed a novel nanocomposite, polyurethane foam impregnated with zero-valent iron nanoparticles (PU@nZVI), for the effective removal of chromium(VI) from various water sources. The characterization of nanocomposite (PU@nZVI) was performed by XRD, SEM-EDS, TEM and FT-IR techniques. Using the response surface methodology, we optimized the removal conditions, achieving an optimal pH of 2 and a dose of 0.5 g/L. The PU@nZVI demonstrated an excellent maximum adsorption capacity of 600.0 mg/g for Cr6+. The adsorption kinetics and isotherms were best described by the pseudo-second-order model and the Freundlich isotherm, respectively. Significantly, the nanocomposite removed 99.98% of Cr6+ from tap water, 96.81% from industrial effluent, and 94.57% from treated sewage wastewater. Furthermore, the PU@nZVI maintained its efficiency over five adsorption-desorption cycles, highlighting its reusability. These results suggest that the PU@nZVI nanocomposite is a highly efficient and sustainable option for chromium(VI) removal in water treatment applications.

Development of an optical sensor for the determination of phenolic compounds in environmental samples.

A new optical sensor was developed for the rapid sensing of total phenolic content, which is simple, cheap, and sensitive, using the Eu(III)-(NTA)2-(Phen) complex [NTA = 1-(2-naphthoyl)-3,3,3-trifluoroacetone and Phen = 1,10 phenanthroline] as a luminescent probe at pH 7.5 using PIPES buffer. This method was based on luminescence quenching. The type of quenching during the reaction between the Eu(III)-(NTA)2-(Phen) complex and the phenolic compounds is dynamic quenching; the binding site is close to 1, and the reaction is endothermic, spontaneous, and involves hydrophobic attraction forces. The calibration curves were plotted using a sigmoidal fit giving an LOD of 0.01 µg mL-1, and the correlation coefficients are more than 0.99. For the first time, the time-resolved fluorescence technique was utilized in microtiter plates to enable the determination of 96 samples within two minutes with high sensitivity and selectivity. The proposed method was applied to three industrial wastewater samples and compared with the standard method for phenolic content determination, yielding high recoveries. This is the first luminescence method based on lanthanide complexes as probes for determining the total phenolic content in water samples.

Evaluation of trace elements concentration using sediments and mussels as bioindicators and pollution indices in the Egyptian Red Sea.

The current work was designed to evaluate the pollution status of the coastline region of the Egyptian Red Sea through monitoring the trace elements in sediments and mussels (Brachidontes variabilis and Modiolus auriculatus) that sampled during winter and summer 2019 from nineteen stations along the investigated area. The analyzed elements showed an annual mean of 20.21, 2.08, 4.79, 46.41, 11.35, 18.14, 128.93 and 12,520.07 µg/g (sediments), 1.02, 0.39, 3.35, 23.73, 0.59, 1.14, 1.43 and 81.94 µg/g (B. variabilis) and 1.39, 0.47, 1.70, 24.69, 0.77, 1.66, 2.16 and 119.80 µg/g (M. auriculatus) for Pb, Cd, Cu, Zn, Co, Ni, Mn and Fe, respectively. The summer recorded highest values of all studied elements in the mussels' species with significant temporal variations (p < 0.05) for the most investigated elements. The pollution indices like CF, PLI, MPI, Igeo and EF were calculated to evaluate the elements contamination degree in the examined areas.

Preparation, characterization and pH-metric measurements of 4-hydroxysalicylidenechitosan Schiff-base complexes of Fe(III), Co(II), Ni(II), Cu(II), Zn(II), Ru(III), Rh(III), Pd(II) and Au(III).

The 4-hydroxysalicylidenechitosan Schiff-base (2CS-Hdhba) was prepared by the condensation of 2,4-dihydroxybenzaldehyde with chitosan, and its metal complexes, [M(2CS-dhba)Cl(2)(H(2)O)(2)] (M(III)=Fe, Ru, Rh), [M'(2CS-dhba)(AcO)(H(2)O)(2)] (M'(II)=Co, Ni, Cu, Zn), [Pd(2CS-dhba)Cl(H(2)O)] and [Au(2CS-dhba)Cl(2)], are reported. These complexes were characterized by elemental analysis, by spectral data (FTIR, solid-phase (13)C NMR, UV-vis and ESR spectroscopy), by morphological observations (SEM and XRD), and by magnetic and thermal measurements. The Schiff base (2CS-Hdhba) behaves as a bidentate chelate with a single negative charge. The azomethine nitrogen and the deprotonated 2-hydroxy centres with the pendant glucosamine hydroxy functionality play no role in coordination. The dissociation constants of 2CS-Hdhba and the stability constants of some of its metal complexes have been determined pH-metrically.