Search Results (23)

Zero-valent iron (ZVI), particularly in its nanoscale form (nZVI), is now considered a highly promising material for the remediation of toxic metal ions from polluted groundwater owing to its strong reductive potential, significant surface area, and reactive behavior. This review systematically explores the application of pristine and modified ZVI systems—including doped ZVI, bio-stabilized composites, and ZVI supported on advanced materials like MXene and nanocellulose—for effective treatment of water containing metal species like As(III/V), Hg(II), Cr(VI), and Ni(II). Emphasis is placed on understanding the underlying mechanisms, including redox reactions, surface complexation, and synergistic adsorption–reduction pathways. Key factors affecting adsorption efficiency—such as pH, temperature, ZVI dosage, and competing ions—are thoroughly analyzed, alongside adsorption kinetics and isotherm models. Modified ZVI composites exhibit enhanced stability, selectivity, and reusability, demonstrating promising performance even in complex aqueous environments. Despite significant progress, challenges such as nanoparticle passivation, limited field-scale data, and potential toxicity of byproducts remain. The review concludes by highlighting future research directions focused on improving material longevity, regeneration efficiency, selective adsorption, and integration with other advanced remediation technologies for sustainable and scalable groundwater treatment. Full article

Nanoparticles are proposed as alternatives to traditional antimicrobial agents. By manipulating a nanoparticle’s core and surface coating, antimicrobial effects against various microbial populations can be customized, known as the “designer effect”. However, the antimicrobial properties of nanoparticle core–coating combinations are understudied; little research exists on their effects on diverse bacteria. The antimicrobial effects of surface-stabilized zero-valent iron nanoparticles (FeNPs) are particularly interesting due to their stability in water and ferromagnetic properties. This study explores the impact of FeNPs coated with three surface coatings on six diverse bacterial species. The FeNPs were synthesized and capped with L-ascorbic acid (AA), cetyltrimethylammonium bromide (CTAB), or polyvinylpyrrolidone (PVP) using a bottom-up approach. Zone of inhibition (ZOI) values, assessed through the disc diffusion assay, indicated that AA-FeNPs and CTAB-FeNPs displayed the most potent antibacterial activity. Bacteria inhibition results ranked from most sensitive to least sensitive are the following: Bacillus nealsonii > Escherichia coli > Staphylococcus aureus > Delftia acidovorans > Chryseobacterium sp. > Sphingobacterium multivorum. Comparisons using ordinal regression and generalized linear mixed models revealed significant differences in bacterial responses to the different coatings and nanoparticle concentrations. The statistical model results are in agreement, thus increasing confidence in these conclusions. This study supports the feasibility of the “designer nanoparticle” concept and offers a framework for future research. Full article

Amid the pressing challenge of global climate change, biogas (marsh gas) has garnered recognition as a clean and renewable energy source with significant potential to reduce greenhouse gas emissions and support sustainable energy production. Composed primarily of methane (CH₄) and carbon dioxide (CO₂), enhancing the CH₄ content in biogas is essential for improving its quality and expanding its high-value applications. This review examines the mechanisms underlying CH₄ and CO₂ production in anaerobic digestion (AD) processes; investigates the effects of raw material types, process routes, and fermentation conditions on biogas production and CH₄ content; and proposes feasible technical pathways for producing CH₄-rich biogas. Research indicates that CH₄-rich biogas can be produced through various strategies. Raw material pretreatment technologies and co-digestion strategies can enhance substrate performance, stabilize the AD process, and boost CH₄ production. Process optimizations, such as multiphase AD and CH₄ co-production techniques, significantly improve carbon utilization efficiency. Introducing exogenous reinforcement materials, including biochar and zero-valent iron nanoparticles, fosters microbial interactions and facilitates direct interspecies electron transfer (DIET). Furthermore, microbial regulation through genetic engineering and microbial community design presents promising prospects. By reviewing the mechanisms of gas production, influencing factors, and feasible pathways, this work aims to provide valuable insights for the technical research of AD to produce CH₄-rich biogas. Full article

Malic acid-derived polyamides, polyhydrazides, and hydrazides exhibit strong potential for a variety of biological applications. This study demonstrates the synthesis of cobalt, silver, copper, zinc, and iron particles by a facile chemical reduction approach utilizing malic acid-derived polyamides, polyhydrazides, and hydrazides as stabilizing and reducing agents. Comprehensive characterization of the particles was performed using UV–Vis spectroscopy, FTIR, XRD, SEM, and EDX analysis. The synthesized particles included both zero-valent metals and oxides exhibiting mixed-phase compositions that may influence their functional properties. UV–vis analysis confirmed the formation of particles represented by the surface plasmon resonance (SPR) peaks specific to each metal particle. FTIR spectroscopy revealed the interaction of the metal particles with the polymer matrix owing to the significant contribution of functional groups in the processes of reduction and stabilization. Further structural insights were obtained via X-ray diffraction (XRD), which identified crystalline phases, and scanning electron microscopy (SEM), which demonstrated uniform morphologies. Additionally, energy-dispersive X-ray (EDX) analysis provided compositional details, affirming the purity and distribution of metallic elements. These findings highlight the potential of malic acid-derived polymers as versatile agents for nanoparticle synthesis with applications in catalysis, sensing, and biomedical technologies. Full article

Nanocomposites (NCs) consisting of zero-valent iron nanoparticles (nZVI) immobilized in chitosan (CS) were prepared and employed for the removal of hexavalent chromium (Cr(VI)) from both synthetic and real wastewater. Medium (MCS)- and high (HCS)-molecular-weight chitosan and stabilization with carboxymethylcellulose (CMC) and different nZVI loads were explored. Characterization through scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDS) and X-ray diffraction (XRD) revealed millimeter-sized spheres with micrometer-sized nZVI clusters randomly distributed. Better nanoparticle dispersion was observed in NCs from the CMC-MCS and HCS combinations. Fourier-transform infrared spectroscopy (FTIR) analysis indicated that CS binds to Fe(II) or Fe(III) on the surface of nZVI through its functional groups -CONH-, -N-H, and -C-OH and through the -${\mathrm{COO}}^{-}$ functional group of CMC, forming a bidentate bridge complex. Through experiments with synthetic waters, it was found that the elimination of Cr(VI) was favored by lowering the pH, obtaining the maximum percentage of Cr(VI) removal at pH 5.5. With real waters, it was shown that increasing the mass of NCs also improved the removal of Cr(VI), following a pseudo-second-order adsorption kinetics. The synthesized materials show great potential for applications in environmental remediation, showing good efficiency in the removal of Cr(VI) in wastewater. Full article

This review article addresses the increasing environmental concerns posed by synthetic dyes in water, exploring innovative approaches for their removal with a focus on zero-valent iron nanoparticles (nZVIs) synthesized through environmentally friendly methods. The article begins by highlighting the persistent nature of synthetic dyes and the limitations of conventional degradation processes. The role of nanoparticles in environmental applications is then discussed, covering diverse methods for metallic nanoparticle production aligned with green chemistry principles. Various methods, including the incorporation of secondary metals, surface coating, emulsification, fixed support, encapsulation, and electrostatic stabilization, are detailed in relation to the stabilization of nZVIs. A novel aspect is introduced in the use of plant extract or biomimetic approaches for chemical reduction during nZVI synthesis. The review investigates the specific challenges posed by dye pollution in wastewater from industrial sources, particularly in the context of garment coloring. Current approaches for dye removal in aqueous environments are discussed, with an emphasis on the effectiveness of green-synthesized nZVIs. The article concludes by offering insights into future perspectives and challenges in the field. The intricate landscape of environmentally friendly nZVI synthesis has been presented, showcasing its potential as a sustainable solution for addressing dye pollution in water. Full article

Here, a comprehensive investigation was conducted under various operational strategies aimed at enhancing biohydrogen production via dark fermentation, with a specific focus on the lactate metabolic pathway, using powdered cheese whey as a substrate. Initially, a batch configuration was tested to determine both the maximum hydrogen yield (100.2 ± 4.2 NmL H₂/g COD_fed) and the substrate (total carbohydrates) consumption efficiency (94.4 ± 0.8%). Subsequently, a transition to continuous operation was made by testing five different operational phases: control (I), incorporation of an inert support medium for biomass fixation (II), addition of carbon-coated, zero-valent iron nanoparticles (CC-nZVI NPs) at 100 mg/L (III), and supplementation of Fe₂O₃ nanoparticles at concentrations of 100 mg/L (IV) and 300 mg/L (V). The results emphasized the critical role of the support medium in stabilizing the continuous system. On the other hand, a remarkable increase of 10% in hydrogen productivity was observed with the addition of Fe₂O₃ NPs (300 mg/L). The analysis of the organic acids’ composition unveiled a positive correlation between high butyrate concentrations and improved volumetric hydrogen production rates (25 L H₂/L-d). Moreover, the presence of iron-based NPs effectively regulated the lactate concentration, maintaining it at low levels. Further exploration of the bacterial community dynamics revealed a mutually beneficial interaction between lactic acid bacteria (LAB) and hydrogen-producing bacteria (HPB) throughout the experimental process, with Prevotella, Clostridium, and Lactobacillus emerging as the predominant genera. In conclusion, this study highlighted the promising potential of nanoparticle addition as a tool for boosting biohydrogen productivity via lactate-driven dark fermentation. Full article

Batch and transport experiments were used to investigate the remediation of loamy sand soil contaminated with Cr(VI) using zero-valent iron nanoparticles (nZVI) stabilized by carboxymethylcellulose (CMC-nZVI). The effect of pH, ionic strength (IS), and flow rate on the removal efficiency of Cr(VI) were investigated under equilibrium (uniform transport) and non-equilibrium (two-site sorption) transport using the Hydrus-1D model. The overall removal efficiency ranged from 70 to over 90% based on the chemical characteristics of the CMC-nZVI suspension and the transport conditions. The concentration and pH of the CMC-nZVI suspension had the most significant effect on the removal efficiency and transport of Cr(VI) in the soil. The average removal efficiency of Cr(VI) was increased from 24.1 to 75.5% when the concentration of CMC-nZVI nanoparticles was increased from 10 to 250 mg L⁻¹, mainly because of the increased total surface area at a larger particle concentration. Batch experiments showed that the removal efficiency of Cr(VI) was much larger under acidic conditions. The average removal efficiency of Cr(VI) reached 90.1 and 60.5% at pH 5 and 7, respectively. The two-site sorption model described (r² = 0.96–0.98) the transport of Cr(VI) in soil quite well as compared to the uniform transport model (r² = 0.81–0.98). The average retardation of Cr(VI) was 3.51 and 1.61 at pH 5 and 7, respectively, indicating earlier arrival for the breakthrough curves and a shorter time to reach maximum relative concentration at lower pH. The methodology presented in this study, combining column experiment and modeling transport using the Hydrus-1D model, successfully assessed the removal of Cr(VI) from polluted soils, offering innovative, cost-effective, and environmentally friendly remediation methodologies. Full article

Soil heavy metal pollution has become an important environmental problem in the world. Therefore, it is particularly important to find effective remediation methods for heavy metal contaminated soil. Biochar (BC) is a kind of soil heavy metal passivator with a wide range of applications. It also has a good effect on the control of soil heavy metal pollution. However, BC does not have sufficient fixation capacity for para-anionic contaminants. Nano-zero-valent iron (nZVI) has a strong reducing ability, which can make up for this defect of BC. Therefore, to improve the passivation effect of heavy metals, nanomaterial modification is proposed to optimize biochar performance. Nanoparticles are used as carriers to impregnate biochar (BC). Biochar-supported nano-ferric zero-valent materials are prepared to repair soil contaminated by heavy metals. Results show that the physicochemical properties of modified biochar are significantly optimized. At 5%, the modified biochar (1:3) treatment group had the best remediation effect on Cd-contaminated soil, which significantly promoted soil catalase activity. The modified biochar (3:1) treatment group had the best remediation effect on As-contaminated soil, and significantly increased soil pH, Cation Exchange Capacity (CEC), and available Fe content. Modified biochar (1:3) with 3% added content was used to repair actual composite heavy metal contaminated soil, and the relative percentage content of Cu, Zn, As, Cd, and Pb residue state increased by 10.28%, 7.81%, 7.44%, 9.26%, and 12.75%, respectively. The effects of nZVI@BC on the remediation effect and soil enzymes of Cd- and As-contaminated soil under different factors such as mass ratio of carbon and iron and dosage were studied. The remediation mechanism of Cd- and As-contaminated soil was clarified, and a good solidification and stabilization effect was obtained. This provides a theoretical basis for nZVI@BC remediation of soil contaminated by Cd and As. It has good application value in the treatment and remediation of complex heavy metal contaminated soil. Full article

Trichloroethylene (TCE) is a prominent groundwater pollutant due to its stability, widespread contamination, and negative health effects upon human exposure; thus, an immense need exists for enhanced environmental remediation techniques. Temperature-responsive domains and catalyst incorporation in membrane domains bring significant advantages for toxic organic decontamination. In this study, hollow fiber membranes (HFMs) were functionalized with stimuli-responsive poly-N-isopropylacrylamide (PNIPAm), poly-methyl methacrylate (PMMA), and catalytic zero-valent iron/palladium (Fe/Pd) for heightened reductive degradation of such pollutants, utilizing methyl orange (MO) as a model compound. By utilizing PNIPAm’s transition from hydrophilic to hydrophobic expression above the LCST of 32 °C, increased pollutant diffusion and adsorption to the catalyst active sites were achieved. PNIPAm-PMMA hydrogels exhibited 11.5× and 10.8× higher equilibrium adsorption values for MO and TCE, respectively, when transitioning from 23 °C to 40 °C. With dip-coated PNIPAm-PMMA-functionalized HFMs (weight gain: ~15%) containing Fe/Pd nanoparticles (d_p~34.8 nm), surface area-normalized rate constants for batch degradation were determined, resulting in a 30% and 420% increase in degradation efficiency above 32 °C for MO and TCE, respectively, due to enhanced sorption on the hydrophobic PNIPAm domain. Overall, with functionalized membranes containing superior surface area-to-volume ratios and enhanced sorption sites, efficient treatment of high-volume contaminated water can be achieved. Full article

The subsurface injection of nanoscale zero-valent iron particles (nZVI) for the in situ reductive remediation of contaminated aquifers has grown over the last 25 years. However, several efforts are still being made to improve the stability and delivery of nZVI and to simplify the procedure for site-specific injection design. In this study, the injectability and mobility of a commercial nZVI-based reactive gel was tested in a radial geometry laboratory setup. The gel proved to be highly mobile in sandy porous media, allowing for the achievement of a radius of influence (ROI) of 0.7 m with a homogeneous nZVI distribution within the domain. The experimental results therefore confirmed that nZVI permeation injection with a good radius of influence is possible in conductive formations. The software MNMs 2023 (Micro- and Nanoparticle transport, filtration, and clogging Model-Suite) was then applied to model the radial transport experiment and extrapolate results with the aim of developing a new graphical tool for simple and effective nZVI permeation injection design. For this purpose, 1800 numerical simulations were performed to build two multiparametric maps to predict the expected ROI in two typical aquifer lithologies and over a wide range of operating conditions. Full article

In the context of the widespread distribution of zero valent iron nanoparticles (nZVI) in the environment and its possible exposure to many aquatic and terrestrial organisms, this study investigates the effects, uptake, bioaccumulation, localisation and possible transformations of nZVI in two different forms (aqueous dispersion—Nanofer 25S and air-stable powder—Nanofer STAR) in a model plant—Arabidopsis thaliana. Seedlings exposed to Nanofer STAR displayed symptoms of toxicity, including chlorosis and reduced growth. At the tissue and cellular level, the exposure to Nanofer STAR induced a strong accumulation of Fe in the root intercellular spaces and in Fe-rich granules in pollen grains. Nanofer STAR did not undergo any transformations during 7 days of incubation, while in Nanofer 25S, three different behaviours were observed: (i) stability, (ii) partial dissolution and (iii) the agglomeration process. The size distributions obtained by SP-ICP-MS/MS demonstrated that regardless of the type of nZVI used, iron was taken up and accumulated in the plant, mainly in the form of intact nanoparticles. The agglomerates created in the growth medium in the case of Nanofer 25S were not taken up by the plant. Taken together, the results indicate that Arabidopsis plants do take up, transport and accumulate nZVI in all parts of the plants, including the seeds, which will provide a better understanding of the behaviour and transformations of nZVI once released into the environment, a critical issue from the point of view of food safety. Full article

Nano zero-valent iron particles (nZVFe) are known as one of the most effective materials for the treatment of contaminated water. However, a strong tendency to agglomerate has been reported as one of their major drawbacks. The present study describes a green approach to synthesizing stabilized nZVFe, using biomass as a porous support material. Therefore, in the first step, biomass-derived activated carbon was prepared by thermochemical procedure from rice straw (RSAC), and then the RSAC-supported nZVFe composite (nZVFe–RSAC) was employed to extract Pb(II) from aqueous solution and was successfully synthesized by the sodium borohydride reduction method. It was confirmed through scanning electron microscopy (SEM) and X-ray diffraction (XRD) characteristics that the nZVFe particles are uniformly dispersed. Results of the batch experiments showed that 6 (g L⁻¹) of this nanocomposite could effectively remove about 97% of Pb(II) ions at pH = 6 from aqueous solution. The maximum adsorption capacities of the RS, RSAC, and nZVFe–RSAC were 23.3, 67.8, and 140.8 (mg g⁻¹), respectively. Based on the results of the adsorption isotherm studies, the adsorption of Pb(II) on nZVFe–RSAC is consistent with the Langmuir–Freundlich isotherm model ${\mathrm{R}}^2=0.996)$. The thermodynamic outcomes exhibited the endothermic, possible, and spontaneous nature of adsorption. Adsorption enthalpy and entropy values were determined as 32.2 kJ mol⁻¹ and 216.9 J mol⁻¹ K⁻¹, respectively. Adsorption kinetics data showed that Pb(II) adsorption onto nZVFe–RSAC was fitted well according to a pseudo-second-order model. Most importantly, the investigation of the adsorption mechanism showed that nZVFe particles are involved in the removal of Pb(II) ions through two main processes, namely Pb adsorption on the surface of nZVFe particles and direct role in the redox reaction. Subsequently, all intermediates produced through the redox reaction between nZVFe and Pb(II) were adsorbed on the nZVFe–RSAC surface. According to the results of the NZVFe–RSAC recyclability experiments, even after five cycles of recovery, this nanocomposite can retain more than 60% of its initial removal efficiency. So, the nZVFe–RSAC nanocomposite could be a promising material for permeable reactive barriers given its potential for removing Pb(II) ions. Due to low-cost and wide availability of iron salts as well as rice biowaste, combined with the high adsorption capacity, make nZVFe–RSAC an appropriate choice for use in the field of Pb(II) removal from contaminated water. Full article

In the current study, lignin, an abundant natural polymer, was dissolved in ethylene glycol and acidic H₂O to form nanoscale lignin. Then, zero-valent iron (ZVI) nanoparticles were synthesized in nanoscale lignin, producing a nZVI/n-lignin composite, via the borohydride reduction method. The use of nZVI/n-lignin for environmental remediation was tested by the removal of methylene blue in aqueous solutions at room temperature. The nZVI/n-lignin composite achieved a higher methylene blue removal ratio than that achieved by traditional nZVIs. Moreover, its excellent dispersibility in water and stability against oxidation in the air were observed. The functions of the nanoscale lignin in the composite material are (1) prevention of further growth and aggregation of the nZVI nanoparticles, (2) protection of nZVI from serious oxidation by H₂O/O₂, and (3) allowing better dispersibility of nZVI in aqueous solutions. These three functions are important for the field applications of nZVI/n-lignin, namely, to travel long distances before making contact with environmental pollutants. The present method for producing nZVI/n-lignin is straightforward, and the combination of nZVI and lignin is an efficient and environmentally friendly material for environmental applications. Full article

Activated zero-valent iron (Ac-ZVI) coupled with Fe³⁺ was employed to activate peroxymonosulfate (PMS) and peroxydisulfate (PDS) for acid orange 7 (AO7) removal. Fe³⁺ was used to promote Fe²⁺ liberation from Ac-ZVI as an active species for reactive oxygen species (ROS) generation. The factors affecting AO7 degradation, namely, the Ac-ZVI:Fe³⁺ ratio, PMS/PDS dosage, and pH, were compared. In both PMS and PDS systems, the AO7 degradation rate increased gradually with increasing Fe³⁺ concentration at fixed Ac-ZVI loading due to the Fe³⁺-promoted liberation of Fe²⁺ from Ac-ZVI. The AO7 degradation rate increased with increasing PMS/PDS dosage due to the greater amount of ROS generated. The degradation rate in the PDS system decreased while the degradation rate in the PMS system increased with increasing pH due to the difference in the PDS and PMS activation mechanisms. On the basis of the radical scavenging study, sulfate radical was identified as the dominant ROS in both systems. The physicochemical properties of pristine and used Ac-ZVI were characterized, indicating that the used Ac-ZVI had an increased BET specific surface area due to the formation of Fe₂O₃ nanoparticles during PMS/PDS activation. Nevertheless, both systems displayed good reusability and stability for at least three cycles, indicating that the systems are promising for pollutant removal. Full article