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Applying nanotechnology, particularly nano zero-valent iron encapsulated by carboxymethyl cellulose (CMC-nZVI), is considered less expensive and provides high efficiency for the decolorization of textile wastewater. In this study, Congo red dye (CR) was used in synthesized wastewater to evaluate the treatment performance using different composition ratios of CMC-nZVI. At the initial CR concentration of 500 mg/L, decolorization efficiencies increased with the increase of CMC contents. The removal efficiencies reached almost completely at the CMC:Fe2+ ratio of 0.004 within 10 seconds after adding CMC-nZVI to the CR solution. The optimal decolorization rate was observed at the Fe concentration of 1 g/L, with the CR removal efficiency of approximately 90% and a removal capacity of 8.298 g CR/g nZVI. The core principle of dye decolorization is breaking down the chromophore groups (-NN-), which makes the color of the dye, into N–H bonds. CMC-nZVI is a promising key to solving the issues caused by dye-containing wastewater.

Membrane-less single-medium sediment microbial fuel cells (single-SMFC) can remove Cu 2+ from sediment through electromigration. However, the high mass transfer resistance of the sediment and amount of oxygen at the cathode of the SMFC limit its Cu 2+ removal ability. Therefore, this study used an oxygen-releasing bead (ORB) for slow oxygen release to increase oxygen at the SMFC cathode and improve the mass transfer property of the sediment. Resultantly, the copper removal efficiency of SMFC increased significantly. Response surface methodology was used to optimize the nano zero-valent iron (nZVI)-modified biochar as the catalyst to enhance the ability of the modified ORB (ORB m ) to remove Cu 2+ and slow release of O 2 . The maximum Cu 2+ removal (95 %) and the slowest O 2 release rate (0.41 mg O 2 /d·g ORB m ) were obtained when the CaO 2 content and ratio of nZVI-modified biochar to unmodified biochar were 0.99 g and 4.95, respectively. When the optimized ORB m was placed at the single-SMFC cathode, the voltage output and copper removal increased by 4.6 and 2.1 times, respectively, compared with the system without ORB m . This shows that the ORB m can improve the migration of Cu 2+ in the sediment, providing a promising remediation method for Cu-contaminated sediments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

This work combined the stability of the porous structure of metal-organic frameworks with the strong reducibility of nano zero-valent iron, for the controllable integration of NZVI into MOFs to utilize the advantages of each component with enhancing the rapid decontamination and scavenging of Cr(VI) from wastewater. Hence, four kinds of MOFs/NZVI composites namely ZIF67/NZVI, MOF74/NZVI, MIL101(Fe)/NZVI, CuBTC/NZVI, were prepared for Cr(VI) capture. The results indicated that the stable structure of ZIF67, MOF74, MIL101(Fe), CuBTC, was beneficial for the dispersion of NZVI that could help more close contact between MOFs/NZVI reactive sites and Cr(VI), subsequently, MOFs/NZVI was proved to be better scavengers for Cr(VI) scavenging than NZVI alone. The Cr(VI) capture achieved the maximum adsorption capacity at pH ~ 4.0, which might be due to the participation of more H + in the reaction and better corrosion of NZVI at lower pH. Mechanism investigation demonstrated synergy of adsorption, reduction and surface precipitation resulted in enhanced Cr(VI) scavenging, and Fe(0), dissolved and surface-bound Fe(II) were the primary reducing species. The findings of this investigation indicated that the as-prepared composites of ZIF67/NZVI, MOF74/NZVI, MIL101(Fe)/NZVI, CuBTC/NZVI, with high oxidation resistance and excellent reactivity, could provide reference for the decontamination and purification of actual Cr(VI)-containing wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Decabromodiphenyl ether (BDE-209) is a common brominated flame retardant in electronic waste, and nano zero-valent iron (nZVI) is a new material in the field of environmental remediation. Little is known about how BDE-209 and nZVI combined exposure influences soil organisms. During the 28 days study, we determined the effects of single and combined exposures to BDE-209 and nZVI on the oxidative stress and metabolic response of earthworms (Eisenia fetida). On day 7, compared to CK, malondialdehyde (MDA) content increased in most combined exposure groups. To remove MDA and reactive oxygen species (ROS), superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD) activities were induced in most combined exposure groups. On day 28, compared to CK, the activities of SOD and CAT were inhibited, while POD activity was significantly induced, indicating that POD plays an important role in scavenging ROS. Combined exposure to BDE-209 and nZVI significantly affected amino acid biosynthesis and metabolism, purine metabolism, and aminoacyl-tRNA biosynthesis pathways, interfered with energy metabolism, and aggravated oxidative stress in earthworms. These findings provide a basis for assessing the ecological impacts of using nZVI to remediate soils contaminated with BDE-209 from electronic waste., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Carbonized bacterial cellulose embedded with highly dispersed nano zero-valent iron (nZVI), denoted as nZVI@CBC, was prepared through one-step in situ carbothermal treatment of bacterial cellulose adsorbing iron(III) nitrate. The structure characteristics of nZVI@CBC and its performance in removing hexavalent chromium Cr(VI) were investigated. Results showed the formation of nZVI@CBC with a surface area of 409.61 m 2 /g at 800 °C, with nZVI particles of mean size 28.2 nm well distributed within the fibrous network of CBC. The stability of nZVI was enhanced by its carbon coating, despite some inevitable oxidation of exposed nZVI. Batch experiments demonstrated that nZVI@CBC exhibited superior removal efficiency compared to bare nZVI and CBC. Under optimal conditions, nZVI@CBC exhibited a high Cr(VI) adsorption capacity of up to 372.42 mg/g. Therefore, nZVI@CBC shows promise as an effective adsorbent for remediating Cr(VI) pollution in water., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Nanoscale zero-valent iron (nZVI) is attracting increasing attention as the most commonly used environmental remediation material. However, given the high surface area and strong reducing capabilities of nZVI, there is a lack of understanding regarding its effects on the complex anaerobic methane production process in flooded soils. To elucidate the mechanism of CH 4 production in soil exposed to nZVI, paddy soil was collected and subjected to anaerobic culture under continuous flooding conditions, with various dosages of nZVI applied. The results showed that the introduction of nZVI into anaerobic flooded rice paddy systems promoted microbial utilization of acetate and carbon dioxide as carbon sources for methane production, ultimately leading to increased methane production. Following the introduction of nZVI into the soil, there was a rapid increase in hydrogen levels in the headspace, surpassing that of the control group. The hydrogen levels in both the experimental and control groups were depleted by the 29th day of culture. These findings suggest that nZVI exposure facilitates the enrichment of hydrogenotrophic methanogens, providing them with a favorable environment for growth. Additionally, it affected soil physicochemical properties by increasing pH and electrical conductivity. The metagenomic analysis further indicates that under exposure to nZVI, hydrogenotrophic methanogens, particularly Methanobacteriaceae and Methanocellaceae, were enriched. The relative abundance of genes such as mcrA and mcrB associated with methane production was increased. This study provides important theoretical insights into the response of key microbes, functional genes, and methane production pathways to nZVI during anaerobic methane production in rice paddy soils, offering fundamental insights into the long-term fate and risks associated with the introduction of nZVI into soils., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

In this study, we synthesized nano zero-valent iron incorporated with a multifunctional molybdenum disulfide film (MoS 2 @nZVI). The material exhibited a 100.00 % removal efficiency for sulfamethoxazole (SMX) and achieved a k obs of 0.4485 min -1 within 10 min. The excellent degradation performance can be attributed to the incorporation of the MoS 2 film, which facilitated Fe 2+ regeneration. Simultaneously, the MoS 2 film assisted in proton accumulation and electron transfer, thereby amplifying the efficiency of SMX degradation across a wide pH range. Comprehensive experimental examinations and characterizations confirmed the selectivity and stability of the MoS 2 @nZVI catalysts, encompassing both degradation efficiency and structural stability. Interestingly, the MoS 2 @nZVI/PMS system for SMX degradation significantly involved a non-radical mechanism ( 1 O 2 ), along with radicals (SO 4 ·- , ·OH, and O 2 ·- ). The direct oxidation of PMS by Fe 2+ not only facilitated the generation of ·OH and SO 4 ·- but also actively engaged in a reaction with O 2 , leading to the production of O 2 ·- . The primary pathway for 1 O 2 production was established through the interplay between Mo 6+ and O 2 ·- , in conjunction with the direct electron transfer (DET) mechanism between PMS and SMX. The contributions of these active species to SMX degradation occurred in the following precedence: SO 4 ·-  >  1 O 2  > ·OH > O 2 ·- . Notably, the primary pathways for radicals and non-radicals were studied during separate reaction periods. This investigation proposed a promising approach for mitigating pharmaceutical pollutants using a transition metal sulfide-modified nZVI catalyst., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Direct electron transfer and the involvement of atomic hydrogen (H ⁎ ) are considered the main mechanisms for reductive dechlorination promoted by nano zero-valent iron (nZVI) supported on highly conductive carbon. It is still unclear how precisely H ⁎ , the specific surface area, and the electrochemical characteristics contribute to biochar supported nano zero-valent iron (BC-nZVI) activity in chlorinated hydrocarbon contaminant removal. In this study, a range of BC-nZVIs were prepared by a liquid-phase reduction process, and the contributions of specific surface area and electrochemical performance to H ⁎ generation and electron transfer have been assessed. The mechanism of trichloroethylene (TCE) dechlorination by BC-nZVIs has been evaluated in terms of removal efficiency and the ultimate degradation products. The results have demonstrated that BC-nZVIs exhibit a higher specific surface area and TCE degradation efficiency compared with the bare nZVI. Ethane, ethylene, and acetylene were the principal TCE degradation products. The elimination of TCE was not significantly affected by differences in BC-nZVI specific surface area, but electron transfer and sustained generation of H ⁎ were dependent on the catalyst electrochemical characteristics. The electrochemical properties of biochar serve to lower the corrosion potential of nZVI, improving electronic transfer capability and reactivity and promoting direct electron transfer for the degradation of TCE. In addition, the enhanced electrochemical properties also facilitate the reaction of nZVI with water and can promote the sustained generation of H ⁎ . Generation of H ⁎ played a key role in reductive dechlorination over BC-nZVIs, which was related to the properties of the biochar support. This study focuses on the role of H ⁎ and electrochemical performance in TCE reductive dechlorination, and provides a theoretical foundation and experimental support for the practical application of BC-nZVIs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

Effective in-situ technology to treat carcinogenic compounds in contaminated areas poses a major challenge. Our objective was to load nano-zero-valent iron (nZVI) onto leonardite char (LNDC), an alternative carbon source from industrial waste, for use as a persulfate (PS) activator for styrene treatment in soil and water. By adding a surfactant during synthesis, cetyltrimethylammonium bromide (CTAB) promotes a flower-like morphology and the nZVI formation in smaller sizes. Results showed that nZVI plays a crucial role in PS activation in both homogeneous and heterogeneous reactions to generate reactive oxygen species (ROS), which can remove 98% of styrene within 20 min. Quenching experiments indicated that singlet oxygen ( 1 O 2 ), superoxide radicals (O 2 •- ), and sulfate radicals (SO 4 •- ) were the main species working together to degrade styrene. XPS analysis also revealed a role of surface oxygen-containing groups (i.e., CO, C-OH) in activating PS for SO 4 •- and 1 O 2 generation. The possible reaction mechanism of PS activation by LNDC-CTAB-nZVI composite and factors affecting treatment efficiency (i.e., PS concentration, catalyst dosage, pH, and humic acid) were illustrated. The molarity/molality ratio of PS to nZVI should be set greater than 1 for effective styrene removal. GC-MS analysis showed that styrene was degraded to a less toxic benzaldehyde intermediate. However, the excessive use of PS and catalysts can harm plant growth, requiring a combining approach to achieve safer use for real applications. Overall results supported the use of the LNDC-CTAB-nZVI/PS system as an efficient in-situ treatment technology for soil and water remediation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

In this study, nano zero-valent iron loaded on biochar (BC-nZVI) was analyzed for its effects on antibiotic resistance genes (ARGs) in composting. The results showed that BC-nZVI increased reactive oxygen species (ROS) production, and the peak values of H 2 O 2 and OH were 22.95 % and 55.30 % higher than those of the control group, respectively. After 65 days, the relative abundances of representative ARGs decreased by 56.12 % in the nZVI group (with BC-nZVI added). An analysis of bacterial communities and networks revealed that Actinobacteria, Proteobacteria, and Firmicutes were the main hosts for ARGs, and BC-nZVI weakened the link between ARGs and host bacteria. Distance-based redundancy analysis showed that BC-nZVI altered the microbial community structure through environmental factors and that most ARGs were negatively correlated with ROS, suggesting that ROS significantly affected the relative abundance of ARGs. According to these results, BC-nZVI showed potential for decreasing the relative abundance of ARGs in composting., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

In this study, novel walnut shell biochar-nano zero-valent iron nanocomposites (WSBC-nZVI) were synthesized using a combined pyrolysis/reduction process. WSBC-nZVI displayed a high removal efficiency (86 %) for carbamazepine (CBZ) compared with walnut shell biochar (70 %) and nano zero-valent iron (76 %) in the presence of persulfate (PS) (0.5 g/L catalyst, 10 mg/L CBZ, 1 mM persulfate). Subsequently, WSBC-nZVI was applied for the fabrication of the membrane using a phase inversion method. The membrane demonstrated an excellent removal efficiency of 91 % for CBZ in a dead-end system (2 mg/L CBZ, 1 mM persulfate). In addition, the effect of various operating conditions on the degradation efficiency in the membrane/persulfate system was investigated. The optimum pH was close to neutral, and an increase in CBZ concentration from 1 mg/L to 10 mg/L led to a drop in removal efficiency from 100 % to 24 %. The degradation mechanisms indicated that oxidative species, including 1 O 2 , OH, SO 4 - , and O 2 - , all contribute to the degradation of CBZ, while the role of 1 O 2 is highlighted. The CBZ degradation products were also investigated, and the possible pathways and the predicted toxicity of intermediates were proposed. Furthermore, the practical use of the membrane was validated by the treatment of real wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Chromium (Cr) accumulating in soil caused serious pollution to cultivated land. At present, nano zero-valent iron (nZVI) is considered to be a promising remediation material for Cr-contaminated soil. However, the nZVI impact on the behavior of Cr in the soil-rice system under high natural geological background value remains unknown. We studied the effects of nZVI on the migration and transformation of Cr in paddy soil-rice by pot experiment. Three different doses of nZVI (0, 0.001 % and 0.1 % (w/w)) treatments and one dose of 0.1 % (w/w) nZVI treatment without plant rice were set up. Under continuous flooding conditions, nZVI significantly increased rice biomass compared with the control. At the same time, nZVI significantly promoted the reduction of Fe in the soil, increased the concentration of oxalate Fe and bioavailable Cr, then facilitated the absorption of Cr in rice roots and the transportation to the aboveground part. In addition, the enrichment of Fe(III)-reducing bacteria and sulfate-reducing bacteria in soil provided electron donors for Cr oxidation, which helps to form bioavailable Cr that is easily absorbed by plants. The results of this study can provide scientific basis and technical support for the remediation of Cr -polluted paddy soil with high geological background., Competing Interests: Declaration of Competing Interest None., (Copyright © 2023 Elsevier B.V. All rights reserved.)

There are increasing concerns about microplastic (MP) pollution in the natural environment. Consequently, numerous physicochemical and toxicological studies have been conducted on the effects of MPs. However, few studies have concerned the potential impact of MPs on contaminated site remediation. We herein investigated the influence of MPs on the temporary and post heavy metal removal by iron nanoparticles, including pristine and sulfurized nano zero-valent irons (nZVI and S-nZVI). MPs inhibited adsorption of most heavy metals during the treatment of iron nanoparticles, and facilitated their desorption, such as Pb (II) from nZVI and Zn (II) from S-nZVI. However, such effects presented by MPs was usually less than those by dissolved oxygen (DO). Most desorption cases are irrelevant to the reduced formats of heavy metals involving redox reactions, such as Cu (I) or Cr (III), suggesting that the influence of MPs on metals are limited to those binding with iron nanoparticles through surface complexation or electrostatic interaction. As another common factor, natural organic matter (NOM) had almost no influence on the heavy metal desorption. These insights shed lights for enhanced remediation of heavy metals by nZVI/S-NZVI in the presence of MPs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Multi-metal contaminated soil has received extensive attention. The biochar and bentonite-supported nano zero-valent iron (nZVI) (BC-BE-nZVI) composite was synthesized in this study by the liquid-phase reduction method. Subsequently, the BC-BE-nZVI composite was applied to immobilize cadmium (Cd), chromium (Cr), and lead (Pb) in simulated contaminated soil. The simultaneous immobilization efficiencies of Cd, Cr(VI), Cr total , and Pb were achieved at 70.95 %, 100 %, 86.21 %, and 100 %, respectively. In addition, mobility and bioavailabilities of Cd, Cr, and Pb were significantly decreased and the risk of iron toxicity was reduced. Stabilized metal species in the contaminated soil (e.g., Cd(OH) 2 , Cd-Fe-(OH) 2 , Cr x Fe 1-x OOH, Cr x Fe 1-x (OH) 3 , PbO, PbCrO 4 , and Pb(OH) 2 ) were formed after the BC-BE-nZVI treatment. Thus, the immobilization mechanisms of Cd, Cr, and Pb, including adsorption, reduction, co-precipitation, and complexation co-exist with the metals. More importantly, bacterial richness, bacterial diversity, soil enzyme activities (dehydrogenase, urease, and fluorescein diacetate hydrolase), and microbial activity were enhanced by applying the BC-BE-nZVI composite, thus increasing the soil metabolic function. Over all, this work applied a promising procedure for remediating multi- metal contaminated soil by using the BC-BE-nZVI composite., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Excessive nitrate has been a critical issue in the water environment, originating from the burning of fossil fuels, inefficient use of nitrogen fertilizers, and discharge of domestic and industrial wastewater. Among the effective treatments for nitrate reduction, electrocatalysis has become an advanced technique because it uses electrons as green reducing agents and can achieve high selectivity through cathode potential control. The effectiveness of electrocatalytic nitrate reduction (NO 3 RR) mainly lies in the electrocatalyst. Iron-based catalysts have the advantages of high activity and low cost, which are well-used in the field of electrocatalytic nitrates. A comprehensive overview of the electrocatalytic mechanism and the iron-based materials for NO 3 RR are given in terms of monometallic iron-based materials as well as bimetallic and oxide iron-based materials. A detailed introduction to NO 3 RR on zero valent iron, single-atom iron catalysts, and Cu/Fe-based bimetallic electrocatalysts are provided, as they are essential for the improvement of NO 3 RR performance. Finally, the advantages of iron-based materials for NO 3 RR and the problems in current applications are summarized, and the development prospects of efficient iron-based catalysts are proposed., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

The integrated system of microbial electrosynthesis (MES) coupled with chain elongation has been considered a promising platform for carboxylic acids production. However, this biotechnology is still in its infancy, and many limitations are needed to be transcended, such as low electron transfer efficiency between cathode and microbes. In this study, nano zero-valent iron (NZVI) was employed to improve carboxylic acid production in the integrated system, and the promotion mechanisms were revealed. Results suggested that the highest production concentrations of acetate, butyrate, and caproate were observed at 7.5 g/L optimized NZVI dosage, increasing the total yield and coulomb efficiency by 23.7 % and 40.3 % compared to the control. Mechanism studies indicated that the hydrogen and electron released by the anaerobic corrosion of NZVI could be used as additional reducing equivalents, thereby enhancing the electron transfer performance. Besides, NZVI was also proven to facilitate the formation of electroactive biofilms according to the results of biofilm characterization and total DNA. In functional microbes' respect, the moderate NZVI enriched the chain elongator in biofilm, like Clostridium_sensu-stricto_12, and upregulated the activities of key enzymes of homoacetogenesis and chain elongation metabolic pathways, like carbon-monoxide dehydrogenase and hydroxyacyl-CoA dehydratase. This study provided the evidence and revealed how NZVI assisted carboxylic acid production from CO 2 via chain elongation in MES., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Antibiotic fermentation residue (AFR) has been categorized as hazardous waste in China. Anaerobic biohydrogen fermentation may be a promising technology for handling AFR, which could achieve dual goals of waste treatment and clean energy production at the same time. However, the low hydrogen yield and low removal efficiency of residual antibiotics are two major factors limiting the AFR biohydrogen fermentation process. This work firstly applied gamma radiation (50 kGy) to remove the residual antibiotic in AFR and improve the bioavailability of organic matters, then adding nano zero-valent iron (nZVI) (100-1000 mg/L) to further enhance the AFR biohydrogen fermentation performance. Results showed that residual deacetoxycephalosporin C in AFR was removed with a high efficiency of 98.6%, and hydrogen yield achieved 20.45 mL/g-VS added with the combined approach of gamma radiation pretreatment and 500 mg/L nZVI addition, which was 139.2% higher compared to the control experimental result. The combined approach also promoted the biohydrogen production rate, decreased the lag phase of hydrogen production, and increased the organics utilization. Microbiological analysis revealed that highly efficient hydrogen-producing genera Clostridium sensu stricto were enriched in much higher abundance with the combined approach, which might be the fundamental mechanism for the enhanced AFR fermentation performance., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Periodate (PI)-based advanced oxidation processes have recently received increasing attentions. Herein, PI was readily activated by nano zero-valent iron (nZVI) and subsequently led to the enhanced oxidation of organic contaminants, with the removal performance of sulfadiazine (SDZ) in the nZVI/PI process even higher than that in the nZVI/peroxydisulfate process under identical conditions. Kinetic experiments indicated that the decay of SDZ was susceptible to the dosage of nZVI and PI, but was barely affected by pH values (4.0-7.0) under buffered conditions, suggesting the promising performance of the nZVI/PI process in a relatively wide pH range. Selective degradation of contaminants and 18 O-isotope labeling assays collectively demonstrated that iodate radical ( • IO 3 ), high-valent iron-oxo species (Fe(IV)) and hydroxyl radical ( • OH) were responsible for the abatement of organic contaminants. More importantly, due to the relatively weak steric hindrance effect of PI, PI easily adsorbed on the surface of nZVI and no iron leaching was detected throughout the reaction, implying that PI activation induced by nZVI was a surface-mediated process. Besides, PI was not transformed into harmful reactive iodine species. This study proposed an environmental-friendly approach for PI activation and shed new lights on the PI-based processes., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Prolonged exposure to inorganic arsenic (As) via drinking water is a major concern as it poses significant human health risks. Removal of As is crucial but requires effective and environment-friendly clean-up technology to avoid any additional risk to the environment. In this study, we developed Australian smectite (smec)-supported nano zero-valent iron (nZVI) composite for arsenate i.e., As(V) sorption. We used a range of tools, including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) and energy dispersion X-ray (EDS) spectroscopy to characterise the material. SEM and TEM images and elemental mapping of the composite reflect that the smectite layer was surrounded by a chain of iron nanobeads evenly distributed on clay particles, which is quite exceptional among currently available nZVIs. The maximum As(V) sorption capacity of this composite was 23.12 mg/g in the ambient conditions. Using X-ray photoelectron spectroscopy we unveiled chemical states of As and Fe before and after the sorption process. Additionally, the release of iron nanoparticles from the composite at various pHs (3-10) were found negligible, which demonstrates the effectiveness of smec-nZVI to remove As(V) from contaminated water without posing any secondary pollutant., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Carboxylate chain elongation is a burgeoning research area for producing added value bio-products from organic fraction of municipal solid waste. Effect of nano zero-valent iron (NZVI) on chain elongation and its possible mechanism was investigated. Highest caproate concentration, 28.0 mmol·L -1 was achieved with 2 g·L -1 NZVI amendment, which is about 16.7% higher than the control. Promoted ethanol utilization was considered as the main reason for the increment of caproate production and hydrogen generation. Electron balance analysis shows that NZVI did not improve the total electron recovery efficiency but favoured the electron flow toward longer carboxylate chain product, i.e. caproate. Finally, full-length 16s rRNA sequencing of bacterial community showed NZVI reshaped the bacterial community by exerting reduction selectivity. And Oscillibacter and Clostridium could be the potential functional species for carboxylate chain elongation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

The extracellular polymeric substances coating magnetic powders-supported nano zero-valent iron (nZVI@EPS@Fe 3 O 4 ) was synthesized, using reduction and adsorption to treat Sb(V) wastewater. The adsorption performance and mechanism were investigated under aerobic and anaerobic conditions. The adsorption capacity of nZVI@EPS@Fe 3 O 4 (79.56 mg/g at pH = 5) was improved compared to that of the original materials (60.74 mg/g). The spectral analysis shows that both nZVI and EPS@Fe 3 O 4 in nZVI@EPS@Fe 3 O 4 played an important role in reducing Sb(V) to Sb(III) and adsorbing Sb. The reducibility and adsorption capacity of nZVI@EPS@Fe 3 O 4 towards Sb(V) remained strong under aerobic condition (62% Sb(III), 79.56 mg/g), although they were slightly weaker than those under anaerobic condition (74% Sb(III), 91.78 mg/g). nZVI@EPS@Fe 3 O 4 showed good performance in regeneration experiments. nZVI@EPS@Fe 3 O 4 is promising as a cost-effective and highly efficient material for Sb(V)-contaminated water. This study is meaningful in understanding the redox behaviour of nZVI composites in aerobic and anaerobic conditions., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Nowadays, the problem of heavy metal pollution in vegetables is received wide attention. In this work, attapulgite clay (ATTP), as a cheap and readily available inorganic mineral material, was modified with nano zero-valent iron (nFe 0 @ATTP) for heavy metal immobilization in soil. Batch experiments were employed to evaluate the optimal remediation performance by ATTP before and after modified with nFe 0 through planting Pakchoi (Brassica chinesis L.) in Cd, Cr, and Pb contaminated soil from Changsha. The results showed that amendments can all increase the pH value of soils, and notably decrease the concentration of extractable Cd, Cr, and Pb in soil. The germination rate and root length of Pakchoi were promoted, and the activities of peroxidase (POD), catalase (CAT), and malondialdehyde (MDA) contents were notably reduced besides superoxide dismutase (SOD) activity after treatments with ATTP and nFe 0 @ATTP. Vicia faba-micronucleus test indicated that the application of amendments reduced the toxicity of heavy metals on the genetic material of Vicia faba root tip cells. The nFe 0 @ATTP were found to well convert Cd, Cr, and Pb into less bioavailable state in soil, thus blocking heavy metal uptake by plants. This material could be a promising amendment for heavy metals contaminated soil., (Copyright © 2019. Published by Elsevier B.V.)

As the functional material, iron nanoparticles effectively promote anaerobic digestion (AD) process, including the hydrolysis-acidification process and the biogas production. In this study, nano zero-valent iron (nZVI) and Fe 3 O 4 nanoparticles (Fe 3 O 4 NPs) were added to AD reactors respectively. The AD process was evaluated by the reactors performances, including pH, biogas yields and compositions, as well as the removal ratio of total solids (TS), volatile solids (VS) and soluble chemical oxygen demand (sCOD). Three models (first-order kinetic model, transfer function model and Cone model) were used to explore the kinetics of AD biogas production. The results showed that adding appropriate dose of nZVI or Fe 3 O 4 NPs enhanced anaerobic digestibility of sludge. The highest cumulative biogas yield of 140.34 L with 0.5 g L -1 nZVI and 137.13 L with 1 g L -1 Fe 3 O 4 NPs were obtained by the 80 days of mesophilic operation, respectively. Cumulative biogas productions of these two reactors were significantly enhanced up to 15.70% and 13.44%. TS removal rates reached >70% in all AD reactors with iron nanoparticles, and the highest sCOD removal rates of nZVI and Fe 3 O 4 NPs digesters on the 80th day were 88.22% and 77.63%, respectively. The results of the three-day fermentation experiment and the kinetic parameters showed that the nZVI or Fe 3 O 4 NPs enhanced the hydrolysis-acidification process of the AD, which eventually promoted biogas production. The Cone model was satisfied with the experimental results, which could be used to evaluate the kinetics of AD with iron nanoparticles more reasonably., (Copyright © 2019 Elsevier B.V. All rights reserved.)

In this study, nano zero valent iron (NZVI) modified MCM-41-zeolite A (Fe-MCM-41-A) composite as a novel adsorbent was prepared by precipitation method and applied for tetracycline (TC) removal from aqueous solution. The adsorbent was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and N 2 -BET analysis. Hysteresis loops indicated that the sample has a desirable magnetic property and can be separated quickly. Adsorption studies were carried out to evaluate its potential for TC removal. Results showed that the optimal Fe-MCM-41-A dosage, initial pH and reaction time at initial TC concentration of 100mgL -1 solution are 1gL -1 , pH=5, and 60 min respectively, at which the removal efficiency of TC was 98.7%. The TC adsorption results fitted the Langmuir isotherm model very well and the adsorption process could be described by a pseudo-second-order kinetic model. A maximum TC adsorption capacity of 526.32mgg -1 was achieved. This study demonstrates that Fe-MCM-41-A is a promising and efficient material for TC adsorption from aqueous solution., (Copyright © 2017 Elsevier B.V. All rights reserved.)

The applicability of bentonite-supported nanoscale zero-valent iron (B-nZVI) as a catalyst to activate persulfate (PS) for the simultaneous removal of Cr(VI) and phenol was systematically investigated in this study. Experimental results demonstrated that phenol degradation was significantly enhanced under acidic condition and with oxygen supply, whereas the Cr(VI) reduction was not obviously declined. The removal efficiencies of Cr(VI) and phenol in B-nZVI/PS combined system were 99.8 and 72.3%, respectively. Cr(VI) reduction and phenol oxidation was simultaneously achieved in B-nZVI/PS combined system, which provided a promising environmental treatment for industrial wastewater containing metal ions and organic compounds. An acidic condition was more favorable to the decomposition of persulfate for the production of sulfate radicals. Radical scavenging tests revealed that the predominant reactive oxygen species for phenol degradation was SO4(-), neither HO nor O2(-). A reaction mechanism, which involves the Cr(VI) removal mainly by the reduction of nZVI and the degradation of phenol mainly by the SO4(-) from the decomposition of persulfate, was proposed. These findings revealed that B-nZVI/PS combined system has a potential in the environmental remediation polluted jointly by organic compounds and/or heavy metals., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Composites of nano zero-valent iron (nZVI) and ordered mesoporous carbon (OMC) are prepared by using simultaneous carbothermal reduction methods. The reactivity and stability of nZVI are expected to be enhanced by embedding it in the ordered pore channels. The structure characteristics of nZVI/OMC and the removal pathway for hexavalent chromium (Cr(VI)) by nZVI/OMC are investigated. Results show that nZVI/OMC with a surface area of 715.16 m(2) g(-1) is obtained at 900 °C. nZVI with particle sizes of 20-30 nm is uniformly embedded in the OMC skeleton. The stability of nZVI is enhanced by surrounding it with a broad carbon layer and a little γ-Fe is derived from the passivation of α-Fe. Detection of ferric state (Fe 2p3/2, around 711.2eV) species confirms that part of the nZVI on the outer surface is inevitably oxidized by O2, even when unused. The removal efficiency of Cr(VI) (50 mg L(-1)) by nZVI/OMC is near 99% within 10 min through reduction (dominant mechanism) and adsorption. nZVI/OMC has the advantage in removal efficiency and reusability in comparison to nZVI/C, OMC and nZVI. This study suggests that nZVI/OMC has the potential for remediation of heavy metal pollution in water., (Copyright © 2015 Elsevier B.V. All rights reserved.)

Iron sulphate (FeSO4) and colloidal nano zero-valent iron (nZVI) as reducing agents were compared, with the aim of assessing their effectiveness in hexavalent chromium [Cr(VI)] removal from a contaminated industrial soil. Experiments were performed on soil samples collected from an industrial site where a nickel contamination, caused by a long-term productive activity, was also verified. The influence of reducing agents amount with respect to chromium content and the effectiveness of deoxygenation of the slurry were discussed. The soil was fully characterized before and after each test, and sequential extractions were performed to assess chemico-physical modifications and evaluate metals mobility induced by washing. Results show that both the reducing agents successfully lowered the amount of Cr(VI) in the soil below the threshold allowed by Italian Environmental Regulation for industrial reuse. Cr(VI) reduction by colloidal nZVI proved to be faster and more effective: the civil reuse of soil [Cr(VI)<2mg/kg] was only achieved using colloidal nZVI within 60min adopting a nZVI/Cr(VI) molar ratio of 30. The reducing treatment resulted in an increase in the amount of chromium in the oxide-hydroxide fraction, thus confirming a mechanism of chromium-iron hydroxides precipitation. In addition, a decrease of nickel (Ni) and lead (Pb) content in soil was also observed when acidic conditions were established., (Copyright © 2014 Elsevier B.V. All rights reserved.)