Search Results (11)

The oxygen evolution reaction (OER) plays a central role as an anode in electrocatalytic processes such as energy conversion and storage and the generation of molecular oxygen from the electrolysis of water. Currently, precious metal oxides such as IrO₂ and RuO₂ are recognized as reference OER electrocatalysts with reasonably high activity; however, their widespread use in practical devices has been severely hindered by their high cost and scarcity. It is essential to design alternative OER electrocatalysts made of low-cost and abundant earth elements with significant activity and robustness. We report four new nanocellulose-derived Fe–zeolite nanocomposites, namely Fe/Zeolite@CCNC (1), Fe/Zeolite@CCNF (2), Fe/Zeolite/CNT@CCNC (3), and Fe/Zeolite/CNT@CCNF (4). Two different types of nanocellulose were investigated: nanocellulose nanofibrils and nanocellulose nanocrystals. Characterization with TEM, SEM-EDS, PXRD, and XPS is reported. The nanocomposites exhibited electrocatalytic activity for OER that varies based on the origin of biocarbon and the composition content. The effect of adding carbon nanotubes to the nanocomposites was studied, and an improvement in OER catalysis was observed. The electrochemical double-layer capacitance and electrochemical impedance spectroscopy of the nanocomposites are reported. The nanocomposite 3 exhibited the highest performance, with an onset potential value of 1.654 V and an overpotential of 551 mV, which exceeds the activity of RuO₂ for OER catalysis at 10 mA/cm² in the glassy carbon electrode. A 24 h chronoamperometry study revealed that the catalyst is active for ~2 h under continuous operating conditions. BET surface analysis showed that the crystalline nanocellulose-derived composite exhibited 301.47 m²/g, and the fibril nanocellulose-derived composite exhibited 120.39 m²/g, indicating that the increased nanoporosity of the former contributes to the increase in OER catalysis. Full article

Adsorption has emerged as a promising method for removing polyphenols in water remediation. This work explores chlorogenic acid (CGA) adsorption on zeolite-based magnetic nanocomposites synthesized from rice husk waste. In particular, enhanced adsorbing materials were attained using a hydrothermal zeolite precursor (Z18) synthesized from rice husk and possessing a remarkable specific surface area (217.69 m² g⁻¹). A composite material was prepared by immobilizing magnetic copper ferrite on Z18 (Z18:CuFe₂O₄) to recover the zeolite adsorbent. In addition, Z18 was modified (Z18 M) with a mixture of 3-aminopropyltriethoxysilane (APTES) and trimethylchlorosilane (TMCS) to improve the affinity towards organic compounds in the final nanocomposite system (Z18 M:CuFe₂O₄). While the unmodified composite demonstrated inconsequential CGA removal rates, Z18 M:CuFe₂O₄ could adsorb 89.35% of CGA within the first hour of operation. Z18 M:CuFe₂O₄ showed no toxicity for seed germination and achieved a mass recovery of 85% (due to a saturation magnetization of 4.1 emu g⁻¹) when an external magnetic field was applied. These results suggest that adsorbing magnetic nanocomposites are amenable to CGA polyphenol removal from wastewater. Furthermore, the reuse, revalorization, and conversion into value-added materials of agro-industrial waste may allow the opportunity to implement sustainability and work towards a circular economy. Full article

In order to enhance the efficiency of heavy metal ion extraction from aqueous medium, new nanocomposite magnetic sorbents were synthesized on the base of natural zeolite (Zt) and nanoparticles of ZnFe₂O₄ (F). The composition, structure and physical–chemical properties of new composites with 2% (Zt-2F), 8% (Zt-8F) and 16% (Zt-16F) of zinc ferrite were characterized by XRD, BET adsorption–desorption of nitrogen, SEM with elemental mapping, TEM and magnetometry. The sorption capacity of materials was assessed towards Cu²⁺ ions in aqueous solutions, for which kinetic and equilibrium features of sorption were established. The maximal sorption capacity (a_max, mg/g) of the studied materials increased in the order: Zt (19.4) < Zt-2F (27.3) < Zt-8F (30.2) < Zt-16F (32.8) < ZnFe₂O₄ (161.3). The kinetics of the sorption process followed a pseudo-second order kinetic model. The sorption equilibrium at zinc ferrite was successfully described by the Langmuir model, while the Freundlich model better fitted the sorption equilibrium on zeolite and composites. The efficiency of Cu²⁺ ion extraction from 320 mg/dm³ aqueous solution was 63% for composite Zt-16F and 100% for a sample of ZnFe₂O₄. It was established that the proposed composite sorbents provide the operation of several cycles without regeneration, they can be easily recycled with 0.1 N HCl solution and are capable of magnetic separation. The advantages of new composites and the proposed method of synthesis allow recommending these materials as effective sorbents of heavy metals from wastewater. Full article

Many contaminants such as heavy metals, dyes and hydrocarbon compounds are annually generated by industrial activities and discharged into water sources. They have destructive impacts on the environment. To eliminate these toxic contaminants from aqueous media, sorption can be considered a proper and efficient process, as it has indicated high efficiency for removing organic contaminants. This paper entails a comprehensive evaluation of different organic pollutants, pros and cons of the sorption process in removing these pollutants, comparing different types of adsorbents and investigating the recyclability of different types of composites. Moreover, the sorption mechanism and kinetic behavior of organic contaminants are investigated using biocomposites and nanocomposites. Moreover, the future perspectives of biocomposites and nanocomposites in eliminating organic compounds are discussed. Based on investigations, a large number of nanocomposites have been utilized for removing organic contaminants with high performance so far, including SiO₂/MnFe₂O₄/ZIF-8 MOF, magnetite/MWCNTs, nano zerovalent iron, barium/Cobalt/polyethylene glycol (PEG), graphene oxide/Fe₃O₄, kaolin/CuFe₂O₄ and Fe₃O₄@UiO-66. Moreover, polyaniline/sodium alginate/Oscillatoria filamentous cyanobacterium biomass, cow bones/zeolite/coconut biocomposite and AC derived from melamine and sucrose are excellent biocomposites in the removal of organic pollutants. Moreover, the reusability study shows that poly(N-isopropylacrylamide)/Fe₃O₄ and corn stalk biomass/chitosan/Fe₃O₄ biocomposites have significant stability compared to other composites in the elimination of organic pollutants. Full article

A core–shell-derived structural magnetic zeolite imidazolate framework-67 (Fe₃O₄-COOH@ZIF-67) nanocomposite was fabricated through a single-step coating of zeolite imidazolate framework-67 on glutaric anhydride-functionalized Fe₃O₄ nanosphere for the magnetic solid-phase extraction (MSPE) of theophylline (TP). The Fe₃O₄-COOH@ZIF-67 nanocomposite was characterized through scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectrometry, Fourier transform infrared spectroscopy, Zeta potential analysis, X-ray diffraction, Brunauer–Emmett–Teller, and vibrating sample magnetometer. The material has a high specific surface area and good magnetism, which maintains the regular dodecahedron structure of ZIF-67 without being destroyed by the addition of Fe₃O₄-COOH nanospheres. The Fe₃O₄-COOH@ZIF-67 can rapidly adsorb TP mainly through the strong coordination interaction between undercoordinated Co²⁺ on ZIF-67 and –NH from imidazole of TP. The adsorption and desorption conditions, such as the amount of adsorbent, adsorption time, pH value, and elution solvent, were optimized. The kinetics of TP adsorption on Fe₃O₄-COOH@ZIF-67 was found to follow pseudo-second-order kinetics. The Langmuir model fits the adsorption data well and the maximum adsorption capacity is 1764 mg/g. Finally, the developed MSPE-HPLC method was applied in the enrichment and analysis of TP in four tea samples and rabbit plasma. TP was not detected in oolong tea and rabbit plasma, and its contents in jasmine tea, black tea, and green tea are 5.80, 4.31, and 1.53 μg/g, respectively. The recoveries of spiked samples are between 74.41% and 86.07% with RSD in the range of 0.81–3.83%. The adsorption performance of Fe₃O₄-COOH@ZIF-67 nanocomposite was nearly unchanged after being stored at room temperature for at least 80 days and two consecutive adsorption–desorption cycles. The results demonstrate that Fe₃O₄-COOH@ZIF-67 nanocomposite is a promising magnetic adsorbent for the preconcentration of TP in complex samples. Full article

This study presents the synthesis of zeolites derived from coal fly ash (CFA) using the fusion-assisted alkaline hydrothermal method. The zeolites were synthesized by combining CFA and NaOH at a molar ratio of 1:1.2 under fusion temperatures of 500, 600, and 700 °C. Subsequently, the obtained zeolites were subjected to further modifications through the incorporation of magnetic (Fe₃O₄) and silver (Ag⁰) nanoparticles (NPs). The Fe₃O₄ NPs were introduced through co-precipitation of Fe(NO₃)₂ and FeCl₃ at a molar ratio of 1:1, followed by thermal curing at 120 °C. On the other hand, the Ag⁰ NPs were incorporated via ion exchange of Na⁺ with Ag⁺ and subsequent reduction using NaBH₄. The synthesized porous materials exhibited the formation of zeolites, specifically analcime and sodalite, as confirmed by X-ray diffraction (XRD) analysis. Additionally, the presence of Fe₃O₄ and Ag⁰ NPs was also confirmed by XRD analysis. The elemental composition analysis of the synthesized nanocomposites further validated the successful formation of Fe₃O₄ and Ag⁰ NPs. Nitrogen porosimetric analysis revealed the formation of a microporous structure, with the BET surface area of the zeolites and nanocomposites ranging from 48.6 to 128.7 m²/g and pore sizes ranging from 0.6 to 4.8 nm. The porosimetric characteristics of the zeolites exhibited noticeable changes after the modification process, which can be attributed to the impregnation of Fe₃O₄ and Ag⁰ NPs. The findings of this research demonstrate the effectiveness of the fusion-assisted method in producing synthetic zeolites and nanocomposites derived from CFA. The resulting composites were evaluated for their potential application in the removal of mercury ions from aqueous solutions. Among the samples tested, the composite containing Ag⁰ NPs exhibited the highest adsorption capacity, reaching 107.4 mg of Hg²⁺ per gram of composite. The composites modified with Fe₃O₄ NPs and Ag/Fe₃O₄ nanocomposites displayed adsorption capacities of 68.4 mg/g and 71.4 mg/g, respectively. Full article

Magnetic nanoparticles are a promising alternative as a support in adsorption processes, aiming at the easy recovery of the aqueous medium. A faujasite zeolite (FAU) surface was decorated with magnesium ferrite (MgFe₂O₄) nanoparticles. FAU is a porous adsorbent with high specific surface area (SSA) and chemical stability. The FAU:MgFe₂O₄ nanocomposite 3:1 ratio (w w⁻¹) promotes the combination of the surface and magnetic properties. The results showed the effectiveness of the MgFe₂O₄ immobilization on the FAU surface, exhibiting a high SSA of 400 m² g⁻¹. The saturation magnetization (Ms) was verified as 5.9 emu g⁻¹ for MgFe₂O₄ and 0.47 emu g⁻¹ for FAU:MgFe₂O₄, an environmentally friendly system with soft magnetic characteristics. The magnetic nanocomposite achieved high adsorption values of around 94% removal for Co²⁺ and Mn²⁺ ions. Regarding its reuse, the nanocomposite preserved adsorption activity of above 65% until the third cycle. Thus, the FAU:MgFe₂O₄ nanocomposite presented favorable adsorptive, magnetic, and recovery properties for reuse cycles in polluted water. Full article

The emergence of mixed matrix membranes (MMMs) or nanocomposite membranes embedded with inorganic nanoparticles (NPs) has opened up a possibility for developing different polymeric membranes with improved physicochemical properties, mechanical properties and performance for resolving environmental and energy-effective water purification. This paper presents an overview of the effects of different hydrophilic nanomaterials, including mineral nanomaterials (e.g., silicon dioxide (SiO₂) and zeolite), metals oxide (e.g., copper oxide (CuO), zirconium dioxide (ZrO₂), zinc oxide (ZnO), antimony tin oxide (ATO), iron (III) oxide (Fe2O3) and tungsten oxide (WO_X)), two-dimensional transition (e.g., MXene), metal–organic framework (MOFs), covalent organic frameworks (COFs) and carbon-based nanomaterials (such as carbon nanotubes and graphene oxide (GO)). The influence of these nanoparticles on the surface and structural changes in the membrane is thoroughly discussed, in addition to the performance efficiency and antifouling resistance of the developed membranes. Recently, GO has shown a considerable capacity in wastewater treatment. This is due to its nanometer-sized holes, ultrathin layer and light and sturdy nature. Therefore, we discuss the effect of the addition of hydrophilic GO in neat form or hyper with other nanoparticles on the properties of different polymeric membranes. A hybrid composite of various NPs has a distinctive style and high-quality products can be designed to allow membrane technology to grow and develop. Hybrid composite NPs could be used on a large scale in the future due to their superior mechanical qualities. A summary and future prospects are offered based on the current discoveries in the field of mixed matrix membranes. This review presents the current progress of mixed matrix membranes, the challenges that affect membrane performance and recent applications for wastewater treatment systems. Full article

This work presents a novel approach to synthesizing magnetic core-shell nanocomposites, consisting of magnetic nanoparticles and a metal-organic framework, for environmental applications. The synthesis is based on the encapsulation of magnetic Fe₃O₄ nanoparticles with microporous zeolitic imidazolate framework-8 (ZIF-8) nanocrystals via ultrasonic activation under a continuous supply of precursor solutions. This sonochemical approach is proven to be a fast, cost-effective, and controllable route for the preparation of magnet-responsive Fe₃O₄@ZIF-8 nanoparticles with a core-shell structure. The functional nanomaterial possesses a high content of ZIF-8 and combined micro/mesoporosity, and thus can be used as adsorbents that can be easily separated using a magnet. In particular, the sonochemically prepared Fe₃O₄@ZIF-8 exhibits significant adsorption performance for the removal of copper ions from water: a short adsorption time (10 min), high maximum uptake capacity (345 mg g⁻¹), and excellent removal efficiency (95.3%). These performances are interpreted and discussed based on the materials characteristics of Fe₃O₄@ZIF-8 established by microscopy, gas sorption, X-ray diffraction, and thermal analysis. Full article

Corrosion-induced iron rust causes severe danger, pollution, and economic problems. In this work, nanopowders of Fe₂O₃ and Fe₂O₃/zeolite are synthesized for the first time using rusted iron waste and natural zeolite heulandite by chemical precipitation. The chemical composition, nanomorphologies, structural parameters, and optical behaviors are investigated using different techniques. The Fe₂O₃/zeolite nanocomposite showed smaller sizes and greater light absorption capability in visible light than Fe₂O₃ nanopowder. The XRD pattern shows crystalline hematite (α-Fe₂O₃) with a rhombohedral structure. The crystallite sizes for the plane (104) of the Fe₂O₃ and Fe₂O₃/zeolite are 64.84 and 56.53 nm, respectively. The Fe₂O₃ and Fe₂O₃/zeolite have indirect bandgap values of 1.87 and 1.91 eV and direct bandgap values of 2.04 and 2.07 eV, respectively. Fe₂O₃ and Fe₂O₃/zeolite nanophotocatalysts are used for solar photoelectrochemical (PEC) hydrogen production. The Fe₂O₃/zeolite exhibits a PEC catalytic hydrogen production rate of 154.45 mmol/g.h @ 1 V in 0.9 M KOH solution, which is the highest value yet for Fe₂O₃-based photocatalysts. The photocurrent density of Fe₂O₃/zeolite is almost two times that of Fe₂O₃ catalyst, and the IPCE (incident photon-to-current conversion efficiency) reached ~27.34%@307 nm and 1 V. The electrochemical surface area (ECSA) values for Fe₂O₃ and Fe₂O₃/zeolite photocatalysts were 7.414 and 21.236 m²/g, respectively. The rate of hydrogen production for Fe₂O₃/zeolite was 154.44 mmol h⁻¹/g. This nanophotocatalyst has a very low PEC corrosion rate of 7.6 pm/year; it can retain ~97% of its initial performance. Therefore, the present research can be applied industrially as a cost-effective technique to address two issues at once by producing solar hydrogen fuel and recycling the rusted iron wires. Full article

This work reports the synthesis of natural zeolite-based silver and magnetite nanocomposites and their application for the catalytic oxidation of methylene blue in water. The zeolite was impregnated with 5.5 wt.% Fe in the form of magnetite nanoparticles with size of 32 nm, and with 6.4 wt.% Ag in the form of silver oxide and metallic silver nanoparticles with sizes of 42 and 20 nm, respectively. The results showed that physical adsorption contributed to the removal of methylene blue by 25–36% and that Fe₃O₄@NZU is superior to Ag₂O@NZU and Ag⁰@NZU, leading to 55% removal without oxidant and 97% in the presence of H₂O₂. However, there is no evidence of significant mineralization of methylene blue. The application of reaction rate models showed that the reaction order changes from zero to first and second order depending on the H₂O₂ concentration. Full article