One of the most significant environmental problems in the world is the massive release of dye wastewater from the dyeing industry. Therefore, the treatment of dyes effluents has received significant attention from researchers in recent years. Calcium peroxide (CP) from the group of alkaline earth metal peroxides acts as an oxidizing agent for the degradation of organic dyes in water. It is known that the commercially available CP has a relatively large particle size, which makes the reaction rate for pollution degradation relatively slow. Therefore, in this study, starch, a non-toxic, biodegradable and biocompatible biopolymer, was used as a stabilizer for synthesizing calcium peroxide nanoparticles (Starch@CPnps). The Starch@CPnps were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Brunauer–Emmet–Teller (BET), dynamic light scattering (DLS), thermogravimetric analysis (TGA), energy dispersive X-ray analysis (EDX) and scanning electron microscopy (SEM). The degradation of organic dyes, methylene blue (MB), using Starch@CPnps as a novel oxidant was studied using three different parameters: initial pH of the MB solution, calcium peroxide initial dosage and contact time. The degradation of the MB dye was carried out via a Fenton reaction, and the degradation efficiency of Starch@CPnps was successfully achieved up to 99%. This study shows that the potential application of starch as a stabilizer can reduce the size of the nanoparticles as it prevents the agglomeration of the nanoparticles during synthesis. Full article

The main objectives of this present paper were to indicate the immobilization of nano zerovalent iron (nZVI) onto a polymeric material (Purolite A400) and the synthesis of the polymeric material (A400-nZVI) through sodium borohydride (NaBH₄) reduction. The obtained polymeric material (A400-nZVI) was used for the nitrate ions removal from a simulated groundwater at different conditions. The polymeric materials, without and with nano zerovalent iron (A400 and A400-nZVI), were characterized trough the FTIR, SEM-EDAX, XRD, and TGA analysis. The analysis confirmed the presence of nano zerovalent iron (nZVI) onto the polymeric material (A400). The adsorption capacity of A400-nZVI, used as polymeric adsorbent, was evaluated by kinetic and thermodynamic studies. The obtained experimental results indicated that the nitrate ions reduction was fitted well by models: pseudo-second-order kinetic and Freundlich isotherm. According to the kinetic model results, a reaction mechanism could exist in the stage of reactions. The higher value of removal nitrate (>80%) was obtained under acidic condition. The results indicated that the obtained polymeric material (A400-nZVI) can be considered as a potential polymeric adsorbent for different pollutants from groundwater and wastewater. Full article

Waste from electrical and electronic equipment (WEEE) is constantly increasing in quantity and becoming more and more heterogeneous as technology is rapidly advancing. The negative impacts it has on human and environment safety, and its richness in valuable rare earth elements (REEs), are accelerating the necessity of innovative methods for recycling and recovery processes. The aim of this work is to comprehend the adsorption and release mechanisms of two different solid sorbents, activated carbon (AC) and its pentaethylenehexamine (PEHA)-modified derivative (MAC), which were deemed adequate for the treatment of REEs deriving from WEEE. Experimental data from adsorption and release tests, performed on synthetic mono-ionic solutions of yttrium, neodymium, and lanthanum, were modelled via linear regression to understand the better prediction between the Langmuir and the Freundlich isotherms for each REE-sorbent couple. The parameters extrapolated from the mathematical modelling were useful to gain an a priori knowledge of the REEs–sorbents interactions. Intraparticle diffusion was the main adsorption mechanism for AC. PEHA contributed to adsorption by means of coordination on amino groups. Release was based on protons fostering both a cation exchange mechanism and protonation. The investigated materials confirmed their potential suitability to be employed in real processes on WEEE at the industrial level. Full article

This work aimed to investigate the degradation performance of natural cellulose acetate (CA) membranes filled with ZnO nanostructures. Photocatalytic degradation of reactive toxic dye methylene blue (MB) was studied as a model reaction using UV light. A CA membrane was previously casted and fabricated through the phase inversion processes and laboratory-synthesized ZnO microparticles as filler. The prepared membrane was characterized for pore size, ultrafiltration (UF) performance, porosity, morphology using scanning electron micrographs (SEM), water contact angle and catalytic degradation of MB. The prepared membrane shows a significant amount of photocatalytic oxidation under UV. The photocatalytic results under UV-light radiation in CA filled with ZnO nanoparticles (CA/ZnO) demonstrated faster and more efficient MB degradation, resulting in more than 30% of initial concentration. The results also revealed how the CA/ZnO combination effectively improves the membrane’s photocatalytic activity toward methylene blue (MB), showing that the degradation process of dye solutions to UV light is chemically and physically stable and cost-effective. This photocatalytic activity toward MB of the cellulose acetate membranes has the potential to make these membranes serious competitors for removing textile dye and other pollutants from aqueous solutions. Hence, polymer–ZnO composite membranes were considered a valuable and attractive topic in membrane technology. Full article

This study is a starting point for the development of an efficient method for rare earths (REs) and transition metals (TMs) recovery from waste electrical and electronic equipment (WEEE) via a hydrometallurgical process. The capture and release capability of mineral clays (STx) and activated carbons (AC), pristine and modified (STx-L6 and AC-L6) with a linear penta-ethylene-hexamine (L6), towards solutions representative of the process, are assessed in the lab-scale. The solids were contacted with synthetic mono- and bi-ionic solutions containing Ni(II) and La(III) in a liquid/solid adsorption process. Contacting experiments were carried out at room temperature for 90 min by fixing a La concentration at 19 mM and varying the Ni one in the range of 19–100 mM. The four solids were able to capture Ni(II) and La(III), both in single- and bi-ionic solutions; however, the presence of the polyamine always results in a large improvement in the capture capability of the pristine sorbents. For all the four solids, capture behaviour is ascribable to an adsorption or ion-sorbent interaction process, because no formation of aquo- and hydroxy-Ni or La can be formed. The polyamine, able to capture Ni ions via coordination, allowed to differentiate ion capture behaviour, thus bypassing the direct competition between Ni and La ions for the capture sites found in the pristine solids. Release values in the 30–100% range were found upon one-step treatment with concentrated HNO₃ solution. However, also, in this case, different metals recovery was found depending on both the sorbent and the ions, suggesting a possible selective recovery. Full article

Hazardous chemicals like toxic organic dyes are very harmful to the environment and their removal is quite challenging. Therefore there is a necessity to develop techniques, which are environment friendly, cost-effective and easily available in nature for water purification and remediation. The present research work is focused on the development` and characterization of the ecofriendly semi-interpenetrating polymer network (semi-IPN) nanocomposite hydrogels composed of polyvinyl alcohol (PVA) and alginate (Alg) hydrogel beads incorporating natural bentonite (Bent) clay as a beneficial adsorbent for the removal of toxic methylene blue (MB) from aqueous solution. PVA−Alg/Bent nanocomposite hydrogel beads with different Bent content (0, 10, 20, and 30 wt%) were synthesized via external ionic gelation method. The designed porous and steady structure beads were characterized by the use of Fourier transform infrared spectroscopy (FTIR), energy-dispersive X-ray spectroscopy (EDX), and scanning electron microscopy (SEM). The performance of the beads as MB adsorbents was investigated by treating aqueous solutions in batch mode. The experimental results indicated that the incorporation of Bent (30 wt%) in the nanocomposite formulation sustained the porous structure, preserved water uptake, and increased MB removal efficiency by 230% compared to empty beads. Designed beads possessed higher affinity to MB at high pH 8, 30 °C, and fitted well to pseudo-second-order kinetic model with a high correlation coefficient. Moreover, the designed beads had good stability and reusability as they exhibited excellent removal efficiency (90%) after six consecutive adsorption-desorption cycles. The adsorption process was found be combination of both monolayer adsorption on homogeneous surface and multilayer adsorption on heterogeneous surface. The maximum adsorption capacity of the designed beads system as calculated by Langmuir isotherm was found to be 51.34 mg/g, which is in good agreement with the reported clay-related adsorbents. The designed semi-IPN PVA−Alg/Bent nanocomposite hydrogel beads demonstrated good adsorbent properties and could be potentially used for MB removal from polluted water. Full article

The goal of the present paper was to synthesize, characterize, and evaluate the performance of the modified composite based on magnetite (Fe₃O₄) and polyvinyl alcohol (PVA). The obtained composite was used to degrade Methyl Orange dye from synthetic wastewater by a laboratory photocatalytic reactor. Various parameters of the photodegradation process were tested: composite dosage, amount of hydrogen peroxide (H₂O₂), and pH. The composite was characterized by Fourier Transform Infrared (FTIR) Spectroscopy, X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). The degradation experiments indicated that the complete dye decolorization depended on the amount of H₂O₂. In addition, the H₂O₂ could accelerate Methyl Orange degradation to more highly oxidized intermediates in the presence of UV light (99.35%). The results suggested that the obtained modified composite could be used to treat wastewater containing various types of dyes. Full article

A new class of conductive metal-organic framework (MOF), polyaniline- aluminum succinate (PANI@Al-SA) nanocomposite was prepared by oxidative polymerization of aniline monomer using potassium persulfate as an oxidant. Several analytical techniques such as FTIR, FE-SEM, EDX, XRD, XPS and TGA-DTA were utilized to characterize the obtained MOFs nanocomposite. DC electrical conductivity of polymer-MOFs was determined by four probe method. A bare glassy carbon electrode (GCE) was modified by nafion/PANI@Al-SA, and examined for Zn (II) ion detection. Modified electrode showed improved efficiency by 91.9%. The modified electrode (PANI@Al-SA/nafion/GCE) exhibited good catalytic property and highly selectivity towards Zn(II) ion. A linear dynamic range of 2.8–228.6 µM was obtained with detection limit of LOD 0.59 µM and excellent sensitivity of 7.14 µA µM⁻¹ cm⁻². The designed procedure for Zn (II) ion detection in real sample exhibited good stability in terms of repeatability, reproducibility and not affected by likely interferents. Therefore, the developed procedure is promising for quantification of Zn(II) ion in real samples. Full article

The effect of copper oxide and zinc oxide nanoparticles (NPs) on the mechanical and thermal properties of ground waste concrete inorganic polymers (GWC IPs) has been investigated. NPs are added to GWC IPs at loadings of 0.1, 0.5, 1, and 2% w/w. The phase composition and microstructure of NPs GWC IPs have also been examined using X-ray diffraction (XRD), Raman spectroscopy and scanning electron microscope (SEM/EDS) techniques. Results show that the mechanical properties of GWC IPs are improved (23 MPa) due to addition of NPs (1% ZnO). In particular, GWC IPs embedded with 0.5% CuO and 1% ZnO NPs exhibited relatively improved compressive strength. The addition of NPs decreases the macroporosity and increases the mesoporosity of IPs matrix and decreases relatively the ability of IPs matrix to water absorption. The antimicrobial activity of GWC IPs doped with 0.5 and 1% CuO NPs against E. coli was also determined. Full article

In this work, we report the synthesis of copper nanoparticles (Cu NPs), employing the chemical reduction method in an aqueous medium. We used copper sulfate pentahydrate (CuSO₄·5H₂O) as a metallic precursor; polyethylenimine (PEI), allylamine (AAM), and 4-aminobutyric acid (AABT) as stabilizing agents; and hydrated hydrazine as a reducing agent. The characterization of the obtained nanoparticles consisted of X-ray, TEM, FTIR, and TGA analyses. Through these techniques, it was possible to detect the presence of the used stabilizing agents on the surface of the NPs. Finally, a zeta potential analysis was performed to differentiate the stability of the nanoparticles with a different type of stabilizing agent, from which it was determined that the most stable nanoparticles were the Cu NPs synthesized in the presence of the PEI/AAM mixture. The antimicrobial activity of Cu/PEI/AABT toward P. aeruginosa and S. aureus bacteria was high, inhibiting both bacteria with low contact times and copper concentrations of 50–200 ppm. The synthesis method allowed us to obtain Cu NPs free of oxides, stable to oxidation, and with high yields. The newly functionalized Cu NPs are potential candidates for antimicrobial applications. Full article

Copper nanoparticles (CuNP) were obtained by a green synthesis method using cotton textile fibers and water as solvent, avoiding the use of toxic reducing agents. The new synthesis method is environmentally friendly, inexpensive, and can be implemented on a larger scale. This method showed the cellulose capacity as a reducing and stabilizing agent for synthetizing Cellulose–Copper nanoparticles (CCuNP). Nanocomposites based on CCuNP were characterized by XRD, TGA, FTIR and DSC. Functional groups present in the CCuNP were identified by FTIR analysis, and XRD patterns disclosed that nanoparticles correspond to pure metallic Cu°, and their sizes are at a range of 13–35 nm. Results demonstrated that CuNPs produced by the new method were homogeneously distributed on the entire surface of the textile fiber, obtaining CCuNP nanocomposites with different copper wt%. Thus, CuNPs obtained by this method are very stable to oxidation and can be stored for months. Characterization studies disclose that the cellulose crystallinity index (CI) is modified in relation to the reaction conditions, and its chemical structure is destroyed when nanocomposites with high copper contents are synthesized. The formation of CuO nanoparticles was confirmed as a by-product, through UV spectroscopy, in the absorbance range of 300–350 nm. Full article

Approximately 200,000 tons of water contaminated with dyes are discharged into effluents annually, which in addition to infectious diseases constitute problems that afflict the population worldwide. This study evaluated the mechanical properties, surface structure, antimicrobial performance, and methylene blue dye-contaminant adsorption using the non-woven fabrics manufactured by melt-blowing. The non-woven fabrics are composed of nylon 6 (Ny 6) and zinc oxide nanoparticles (ZnO NPs). The polymer nanocomposites were previously fabricated using variable frequency ultrasound assisted-melt-extrusion to be used in melt-blowing. Energy dispersion spectroscopy (SEM-EDS) images showed a homogeneous dispersion of the ZnO nanoparticles in nylon 6. The mechanical properties of the composites increased by adding ZnO compared to the nylon 6 matrix, and sample Ny/ZnO 0.5 showed the best mechanical performance. All fabric samples exhibited antimicrobial activity against S. aureus and fungus C. albicans, and the incorporation of ZnO nanoparticles significantly improved this property compared to pure nylon 6. The absorption efficiency of methylene blue (MB), during 60 min, for the samples Ny/ZnO 0.05 and Ny/ZnO 0.25 wt%, were 93% and 65%, respectively. The adsorption equilibrium data obeyed the Langmuir isotherm. Full article

Polypyrrole (PPy) and polypyrrole/cerium oxide nanocomposite (PPy/CeO₂) were prepared by the chemical oxidative method in an aqueous medium using anhydrous ferric chloride (FeCl₃) as an oxidant. The successful formulation of materials was confirmed by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and transmittance electron microscopy (TEM). A four-in-line probe device was used for studying DC electrical conductivity and ammonia vapor sensing properties of PPy and PPy/CeO₂. The significant improvement in both the conductivity and sensing parameters of PPy/CeO₂ compared to pristine PPy reveals some synergistic/electronic interaction between PPy and cerium oxide nanoparticles (CeO₂ NPs) working at molecular levels. The initial conductivity (i.e., conductivity at room temperature) was found to be 0.152 Scm⁻¹ and 1.295 Scm⁻¹ for PPy and PPy/CeO₂, respectively. Also, PPy/CeO₂ showed much better conductivity retention than pristine PPy under both the isothermal and cyclic ageing conditions. Ammonia vapor sensing was carried out at different concentration (0.01, 0.03, 0.05, 0.1, 0.2, 0.3, 0.4, and 0.5 vol %). The sensing response of PPy/CeO₂ varied with varying concentrations. At 0.5 vol % ammonia concentration, the % sensing response of PPy and PPy/CeO₂ sensor was found to be 39.1% and 93.4%, respectively. The sensing efficiency of the PPy/CeO₂ sensor was also evaluated at 0.4. 0.3, 0.2, 0.1, 0.05, 0.03, and 0.01 vol % ammonia concentration in terms of % sensing response, response/recovery time, reversibility, selectivity as well as stability at room temperature. Full article

Towards the utilization of Cu₂O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu₂O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu₂O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu₂O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu₂O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples. Full article

Phenol is regarded as a major pollutant, as the toxicity levels are in the range of 9–25 mg/L for aquatic life and humans. This study embedded silica sodalite (SSOD) and hydroxy sodalite (HSOD) nanoparticles into polysulfone (PSF) for enhancement of its physicochemical properties for treatment of phenol-containing wastewater. The pure polysulfone membranes and sodalite-infused membranes were synthesized via phase inversion. To check the surface morphology, surface hydrophilicity, surface functionality, surface roughness and measure the mechanical properties of the membranes, characterization techniques such as Scanning Electron Microscope (SEM), contact angle measurements, Fourier Transform Infrared, Atomic Force Microscopy (AFM) nanotensile tests were used, respectively. The morphology of the composite membranes showed incorporation of the sodalite crystals decreased the membrane porosity. The results obtained showed the highest contact angle of 83.81° for pure PSF as compared to that of the composite membranes. The composite membranes with 10 wt.% HSOD/PSF and 10 wt.% SSOD/PSF showed mechanical enhancement as indicated by a 20.96% and 19.69% increase in ultimate tensile strength, respectively compared to pure PSF. The performance evaluation of the membranes was done using a dead-end filtration cell at varied feed pressure. Synthetic phenol-containing wastewater was prepared by dissolving one gram of phenol crystals in 1 L of deionized water and used in this study. Results showed higher flux for sodalite infused membranes than pure PSF for both pure and phenol-containing water. However, pure PSF showed the highest phenol rejection of 93.55% as compared to 63.65% and 64.75% achieved by 10 wt.% HSOD/PSF and 10 wt.% SSOD/PSF, respectively. The two sodalite infused membranes have shown enhanced mechanical properties and permeability during treatment of phenol in synthetic wastewater. Full article

Over the years, the persistent occurrence of superfluous endocrine-disrupting compounds (EDCs) (sub µg L⁻¹) in water has led to serious health disorders in human and aquatic lives, as well as undermined the water quality. At present, there are no generally accepted regulatory discharge limits for the EDCs to avert their possible negative impacts. Moreover, the conventional treatment processes have reportedly failed to remove the persistent EDC pollutants, and this has led researchers to develop alternative treatment methods. Comprehensive information on the recent advances in the existing novel treatment processes and their peculiar limitations is still lacking. In this regard, the various treatment methods for the removal of EDCs are critically studied and reported in this paper. Initially, the occurrences of the EDCs and their attributed effects on humans, aquatic life, and wildlife are systematically reviewed, as well as the applied treatments. The most noticeable advances in the treatment methods include adsorption, catalytic degradation, ozonation, membrane separation, and advanced oxidation processes (AOP), as well as hybrid processes. The recent advances in the treatment technologies available for the elimination of EDCs from various water resources alongside with their associated drawbacks are discussed critically. Besides, the application of hybrid adsorption–membrane treatment using several novel nano-precursors is carefully reviewed. The operating factors influencing the EDCs’ remediations via adsorption is also briefly examined. Interestingly, research findings have indicated that some of the contemporary techniques could achieve more than 99% EDCs removal. Full article

Polycyclic aromatic hydrocarbons (PAHs) are a class of naturally occurring chemicals resulting from the insufficient combustion of fossil fuels. Among the PAHs, phenanthrene is one of the most studied compounds in the marine ecosystems. The damaging effects of phenanthrene on the environment are increasing day by day globally. To lessen its effect on the environment, it is essential to remove phenanthrene from the water resources in particular and the environment in general through advanced treatment methods such as photocatalytic degradation with high-performance characteristics and low cost. Therefore, the combination of metals or amalgamation of bimetallic oxides as an efficient photocatalyst demonstrated its propitiousness for the degradation of phenanthrene from aqueous solutions. Here, we reviewed the different nanocomposite materials as a photocatalyst, the mechanism and reactions to the treatment of phenanthrene, as well as the influence of other variables on the rate of phenanthrene degradation. Full article