Iron Redox Research Articles

Effect of Pore Formation on Redox-Driven Phase Transformation.

When solid-state redox-driven phase transformations are associated with mass loss, vacancies are produced that develop into pores. These pores can influence the kinetics of certain redox and phase transformation steps. We investigated the structural and chemical mechanisms in and at pores in a combined experimental-theoretical study, using the reduction of iron oxide by hydrogen as a model system. The redox product (water) accumulates inside the pores and shifts the local equilibrium at the already reduced material back toward reoxidation into cubic Fe_{1-x}O (where x refers to Fe deficiency, space group Fm3[over ¯]m). This effect helps us to understand the sluggish reduction of cubic Fe_{1-x}O by hydrogen, a key process for future sustainable steelmaking.

Reduce methane emission from rice paddies by man-made aerenchymatous tissues

Methane is the second most important greenhouse gas after carbon dioxide, and 8–11% is emitted from paddy fields. Methanogenic microbial processes in water-saturated soils can be alleviated through the oxygenation of soils, which may hamper methane production and emissions in paddies. Here, by mimicking O2 release from rice roots, we report the use of man-made (i.e., silicone tube-based) aerenchymatous tissues (MAT) to continuously release O2 to abate methane emission from paddies. High O2-releasing rates (such as 5 kg O2/ha/d) can be easily achieved by adjusting MAT density (e.g., 0.2 m2 tube/m2 soil) and its inner air pressure (e.g., 25 kPa). Following deployment, MAT significantly increased soil redox potential (from -150 mV to -88.6 mV) and induced active iron redox cycling. This decreased the availability of organic substrates of methanogens and therefore dramatically reduced their abundance (-25.1% active mcrA gene). We quantified the decrease in methane emission both in mesocosms and paddy field trials and found in both setups that ~ 50% of methane emission was reduced. Moreover, we showed that the performance of MAT can be further improved by simply increasing the air pressure in MAT (e.g., -74.2% methane emission at 200 kPa air pressure). This work provides a powerful and sustainable method for mitigating methane emission from rice paddies.Graphical

Magnetic carbon nanocomposites via the graphitization of glucose and their induction heating

Carbon nanocomposites containing iron-based nanoparticles are attractive materials for the catalyst supports used for magnetic (induction) heating catalysis. The metallic, soft-magnetic iron nanoparticles provide local heating of the support in an alternating magnetic field and ensure rapid magnetic separation of the nanocomposite particles from reaction suspensions. In this work, magnetic carbon nanocomposites were prepared by annealing the precursor particles consisting of iron-oxide nanoparticles dispersed in a carbohydrate matrix. The annealing was conducted at 600 °C and 750 °C in an Ar atmosphere. At both temperatures the carbothermal reduction of iron oxide to Fe/Fe3C was observed; however, at the lower temperature the rate of reduction and the growth of the nanoparticles were considerably slower. The Fe3C was formed in negligible amounts only after a prolonged period of annealing at 600 °C. A detailed structural analysis showed that the Fe/Fe3C nanoparticles catalyze the graphitization of the carbonaceous precursor material already at 600 °C, resulting in the formation of a graphitic shell that surrounds them. This shell is tight enough to prevent the areal oxidation of the encapsulated Fe nanoparticles; their magnetic properties remained unchanged even after 1 year of storage under ambient conditions. At the higher annealing temperature, the growth of the Fe/Fe3C nanoparticles caused bursting of the graphitic shell and thus partially exposed their surfaces to the atmosphere. All the nanocomposites exhibited ferromagnetic behavior in accordance with their compositions. The nanocomposite that was predominantly composed of a graphitic shell, encapsulated Fe nanoparticles and a negligible amount of Fe3C, showed the highest specific absorption rate (760 W/gFe at 274 kHz), even at a relatively low AC-field amplitude (88 mT).

Microbial reduction and alteration of Fe(III)-containing smectites in the presence of biochar-derived dissolved organic matter

Clay minerals are important components of solid-phase iron pools in soils, and the redox state of structurally-coordinated iron in clay minerals can significantly influence soil physicochemical properties. Due to increasing use of biochar in agriculture, the dissolved organic matter derived from biochar (BDOM) has become an unignorable fraction of dissolved organic carbon in soil systems. However, our knowledge regarding the effect of BDOM on soil biogeochemical processes (particularly on iron redox cycling) is still very limited. To examine the role of BDOM in the microbial reduction of Fe(III) in clays, BDOM was extracted from wheat straw biochar and selectively added to laboratory reactors in which lactate, Fe(III)-containing smectite (montmorillonite SWy-2 or nontronite NAu-2), and a typical iron-reducing bacterium Shewanella oneidensis strain MR-1 were used as the respective electron donor, electron acceptor, and reaction mediator. The results demonstrated that BDOM contained bio-reactive quinone moieties. BDOM amendment increased the initial rate and final extent of Fe(III) bioreduction by strain MR-1. Such promotion effect of BDOM might be ascribed to its quinone moieties functioning as electron shuttles between MR-1 cells and structural Fe(III) in smectite. Structural changes were observed in the bioreduced smectite systems, especially for NAu-2 reactors in which obvious dissolution and illitization occurred. These observations suggest that BDOM is bio-reactive and is able to stimulate the microbial reduction of Fe(III) in clay minerals, and may offer new insights into the effects of biochar application in elemental cycles in soils.

Sulfur_X: A Model of Sulfur Degassing During Magma Ascent

AbstractThe degassing of CO2 and S from arc volcanoes is fundamentally important to global climate, eruption forecasting, ore deposits, and the cycling of volatiles through subduction zones. However, all existing thermodynamic/empirical models have difficulties reproducing CO2‐H2O‐S trends observed in melt inclusions and provide widely conflicting results regarding the relationships between pressure and CO2/SO2 in the vapor. In this study, we develop an open‐source degassing model, Sulfur_X, to track the evolution of S, CO2, H2O, and redox states in melt and vapor in ascending mafic‐intermediate magma. Sulfur_X describes sulfur degassing by parameterizing experimentally derived sulfur partition coefficients for two equilibria: RxnI. FeS (m) + H2O (v) H2S (v) + FeO (m), and RxnII. CaSO4(m) SO2 (v) + O2 (v) + CaO (m), based on the sulfur speciation in the melt (m) and co‐existing vapor (v). Sulfur_X is also the first to track the evolution of fO2 and sulfur and iron redox states accurately in the system using electron balance and equilibrium calculations. Our results show that a typical H2O‐rich (4.5 wt.%) arc magma with high initial S6+/ΣS ratio (>0.5) will degas much more (∼2/3) of its initial sulfur at high pressures (>200 MPa) than H2O‐poor ocean island basalts with low initial S6+/ΣS ratio (<0.1), which will degas very little sulfur until shallow pressures (<50 MPa). The pressure‐S relationship in the melt predicted by Sulfur_X provides new insights into interpreting the CO2/ST ratio measured in high‐T volcanic gases in the run‐up to the eruption.

Reducing Iron Oxide with Ammonia: A Sustainable Path to Green Steel.

Iron making is the biggest single cause of global warming. The reduction of iron ores with carbon generates about 7% of the global carbon dioxide emissions to produce ≈1.85 billion tons of steel per year. This dramatic scenario fuels efforts to re-invent this sector by using renewable and carbon-free reductants and electricity. Here, the authors showhow to make sustainable steel by reducing solid iron oxides with hydrogen released from ammonia. Ammonia is an annually 180 million ton traded chemical energy carrier, with established transcontinental logistics and low liquefaction costs. It can be synthesized with green hydrogen and release hydrogen again through the reduction reaction. This advantage connects it with green iron making, for replacing fossil reductants. the authors show that ammonia-based reduction of iron oxide proceeds through an autocatalytic reaction, is kinetically as effective as hydrogen-based direct reduction, yields the same metallization, and can be industrially realized with existing technologies. The produced iron/iron nitride mixture can be subsequently melted in an electric arc furnace (or co-charged into a converter) to adjust the chemical composition to the target steel grades. A novel approach is thus presented to deploying intermittent renewable energy, mediated by green ammonia, for a disruptive technology transition toward sustainable iron making.

A Review on the Modeling of Direct Reduction of Iron Oxides in Gas‐Based Shaft Furnaces

Although the blast furnace process is the dominant ironmaking route to supply the feedstocks for steelmaking, a number of alternative ironmaking technologies such as the direct reduction process have grown rapidly in recent decades. This development is largely in response to the increasingly stringent emission control policies, rising costs of energy, and the increasing costs and environmental effects of coke usage. In direct reduction processes, iron oxides are reduced to iron at a temperature below its melting point. More than 79% of direct reduced iron is produced by Midrex and Energiron, both of which use gas‐based shaft furnaces. A proper understanding of these processes is required to improve the performance and operation of the plants based on them. Therefore, herein, it is aimed to provide a comprehensive review of research that is carried out over the last several decades to examine the effects of the important phenomena on the performance of the gas‐based shaft furnaces. The review is divided into experimental and mathematical investigations. The main features, limitations, and shortcomings of each study are discussed. Finally, the review concludes with current knowledge gaps and suggestions for further research in this thriving sector of the steel industry.

Aerobic Denitrification Enhanced by Immobilized Slow-Released Iron/Activated Carbon Aquagel Treatment of Low C/N Micropolluted Water: Denitrification Performance, Denitrifying Bacterial Community Co-occurrence, and Implications.

The key limiting factors in the treatment of low C/N micropolluted water bodies are deficient essential electron donors for nitrogen removal processes. An iron/activated carbon aquagel (IACA) was synthesized as a slowly released inorganic electron donor to enhance aerobic denitrification performance in low C/N micropolluted water treatment. The denitrification efficiency in IACA reactors was enhanced by more than 56.72% and the highest of 94.12% was accomplished compared with those of the control reactors. Moreover, the CODMn removal efficiency improved by more than 34.32% in IACA reactors. The Illumina MiSeq sequencing consequence explained that the denitrifying bacteria with facultative denitrification, iron oxidation, and iron reduction function were located in the dominant species niches in the IACA reactors (e.g., Pseudomonas, Leptothrix, and Comamonas). The diversity and richness of the denitrifying bacterial communities were enhanced in the IACA reactors. Network analysis indicated that aerobic denitrifying bacterial consortia in IACA reactors presented a more complicated co-occurrence structure. The IACA reactors presented the potential for long-term denitrification operation. This study affords a pathway to utilize IACA, promoting aerobic denitrification during low C/N micropolluted water body treatment.

GSH and H2O2 dynamic correlation in the ferroptosis pathways revealed by engineered probe in tumor and kidney injury

Ferroptosis is a cell death mode of lipid peroxidation caused by iron metabolism disorder and redox imbalance, which is closely associated with the evolution of tumour and ischemia reperfusion injury and other diseases, and it involves the excessive accumulation of reactive oxygen species promoting ferroptosis pathway and thiols-associated anti-ferroptosis pathway. To study the dynamic correlation between reactive oxygen species and active sulfur in the two pathways is of great significance for revealing the precise regulation mechanism of ferroptosis. Hydrogen peroxide (H2O2) and glutathione (GSH), as very active redox species in organisms, participate dynamically in the ferroptosis process. In this study, hemicyanine dye conjugated H2O2 specific response site were coupled with coumarin derivative containing GSH specific response site, realizing distinguishing simultaneous detection of H2O2 and GSH through near-infrared and cyan fluorescence emission after response. At the cellular level, the dynamic correlation between H2O2 and GSH in the ferroptosis pathway was explored, and the synergistic ferroptosis inducer was screened for further application at the tumor level, then monitoring the process of ferroptosis inducer used for tumor ablation and ferroptosis inhibitor used to alleviate kidney ischemia–reperfusion injury by fluorescence imaging.

CFD Modelling of Gas-Solid Reactions: Analysis of Iron and Manganese Oxides Reduction with Hydrogen

Metallurgical processes are characterized by a complex interplay of heat and mass transfer, momentum transfer, and reaction kinetics, and these interactions play a crucial role in reactor performance. Integrating chemistry and transport results in stiff and non-linear equations and longer time and length scales, which ultimately leads to a high computational expense. The current study employs the OpenFOAM solver based on a fictitious domain method to analyze gas-solid reactions in a porous medium using hydrogen as a reducing agent. The reduction of oxides with hydrogen involves the hierarchical phenomena that influence the reaction rates at various temporal and spatial scales; thus, multi-scale models are needed to bridge the length scale from micro-scale to macro-scale accurately. As a first step towards developing such capabilities, the current study analyses OpenFOAM reacting flow methods in cases related to hydrogen reduction of iron and manganese oxides. Since reduction of the oxides of interest with hydrogen requires significant modifications to the current industrial processes, this model can aid in the design and optimization. The model was verified against experimental data and the dynamic features of the porous medium observed as the reaction progresses is well captured by the model.

Conjugative plasmids inhibit extracellular electron transfer in Geobacter sulfurreducens.

Geobacter sulfurreducens is part of a specialized group of microbes with the unique ability to exchange electrons with insoluble materials, such as iron oxides and electrodes. Therefore, G. sulfurreducens plays an essential role in the biogeochemical iron cycle and microbial electrochemical systems. In G. sulfurreducens this ability is primarily dependent on electrically conductive nanowires that link internal electron flow from metabolism to solid electron acceptors in the extracellular environment. Here we show that when carrying conjugative plasmids, which are self-transmissible plasmids that are ubiquitous in environmental bacteria, G. sulfurreducens reduces insoluble iron oxides at much slower rates. This was the case for all three conjugative plasmids tested (pKJK5, RP4 and pB10). Growth with electron acceptors that do not require expression of nanowires was, on the other hand, unaffected. Furthermore, iron oxide reduction was also inhibited in Geobacter chapellei, but not in Shewanella oneidensis where electron export is nanowire-independent. As determined by transcriptomics, presence of pKJK5 reduces transcription of several genes that have been shown to be implicated in extracellular electron transfer in G. sulfurreducens, including pilA and omcE. These results suggest that conjugative plasmids can in fact be very disadvantageous for the bacterial host by imposing specific phenotypic changes, and that these plasmids may contribute to shaping the microbial composition in electrode-respiring biofilms in microbial electrochemical reactors.

Assessing phosphorus availability in paddy soils: the importance of integrating soil tests and plant responses

Phosphorus (P) cycling in paddy soil is closely related to iron (Fe) redox wheel; its availability to rice has thus generally been ascribed to Fe minerals reductive dissolution. However, the literature aimed to identify the best method for predicting rice available P does not uniformly point to Fe reductants. Rice plants can indeed solubilize and absorb P through many strategies as a function of P supply, modifying the chemical environment. Therefore, this study aims to estimate P availability in paddy soils coupling the redox mechanisms driving P cycling with concurrent plant responses. Soil available P was estimated in three groups of paddy soils with low, medium, or high P content assessing easily desorbable pools (0.01 M calcium chloride, Olsen, Mehlich-III, anion exchanging resins) and Fe-bound P pools (EDTA, citrate-ascorbate, and oxalate). Rice P uptake and responses to P availability were assessed by a mesocosm cultivation trial. Although P released in porewater positively correlated with dissolved Fe(II), it did not with plant P uptake, and readily desorbable P pools were better availability predictors than Fe-bound pools, mainly because of the asynchrony observed between Fe reduction and plant P demand. Moreover, in low P soils, plants showed higher Fe(II) oxidation, enhanced root growth, and up-regulation of P root transporter encoding genes, plant responses being related with changes in P pools. These results indicate the generally assumed direct link between Fe reduction and rice P nutrition in paddy soils as an oversimplification, with rice P nutrition appearing as the result of a complex trade-off between soil redox dynamics, P content, and plant responses.

Ferroptotic mechanisms and therapeutic targeting of iron metabolism and lipid peroxidation in the kidney.

Ferroptosis is a mechanism of regulated necrotic cell death characterized by iron-dependent, lipid peroxidation-driven membrane destruction that can be inhibited by glutathione peroxidase 4. Morphologically, it is characterized by cellular, organelle and cytoplasmic swelling and the loss of plasma membrane integrity, with the release of intracellular components. Ferroptosis is triggered in cells with dysregulated iron and thiol redox metabolism, whereby the initial robust but selective accumulation of hydroperoxy polyunsaturated fatty acid-containing phospholipids is further propagated through enzymatic and non-enzymatic secondary mechanisms, leading to formation of oxidatively truncated electrophilic species and their adducts with proteins. Thus, ferroptosis is dependent on the convergence of iron, thiol and lipid metabolic pathways. The kidney is particularly susceptible to redox imbalance. A growing body of evidence has linked ferroptosis to acute kidney injury in the context of diverse stimuli, such as ischaemia-reperfusion, sepsis or toxins, and to chronic kidney disease, suggesting that ferroptosis may represent a novel therapeutic target for kidney disease. However, further work is needed to address gaps in our understanding of the triggers, execution and spreading mechanisms of ferroptosis.

Preparation and application of red mud-based heterogeneous Fenton catalyst

The zero-valent iron (ZVI) heterogeneous Fenton catalyst based on red mud (RM) was synthesized by direct reducing iron oxide in RM using H2 at 800 °C (RMH-800). X-ray diffraction analysis showed that Fe2O3 in RM was reduced to Fe0. Brunauer -Emmett-Teller, scanning electron microscopy and high-resolution transmission electron microscopy show that RMH-800 is a ZVI-loaded porous material. The catalysts were characterized by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Under the conditions of 2.86 mM H2O2, 100 mg/L Acid Red G (ARG) and 1 g/L RMH-800, 95 % of ARG was removed within 10 min. The RMH-800/H2O2 system also showed excellent degradability to antibiotics (Sulfamethoxazole, Ibuprofen and Primidone). •OH is the main species responsible for pollutants degradation. RMH-800 showed low iron leaching during the reaction process and excellent catalytic performance even after 6 repeats, indicating it a stable and low-cost material with great potential for wastewater treatment.

CYB5R3 in type II alveolar epithelial cells protects against lung fibrosis by suppressing TGF-β1 signaling.

Type II alveolar epithelial cell (AECII) redox imbalance contributes to the pathogenesis of idiopathic pulmonary fibrosis (IPF), a deadly disease with limited treatment options. Here, we show that expression of membrane-bound cytochrome B5 reductase 3 (CYB5R3), an enzyme critical for maintaining cellular redox homeostasis and soluble guanylate cyclase (sGC) heme iron redox state, is diminished in IPF AECIIs. Deficiency of CYB5R3 in AECIIs led to sustained activation of the pro-fibrotic factor TGF-β1 and increased susceptibility to lung fibrosis. We further show that CYB5R3 is a critical regulator of ERK1/2 phosphorylation and the sGC/cGMP/protein kinase G axis that modulates activation of the TGF-β1 signaling pathway. We demonstrate that sGC agonists (BAY 41-8543 and BAY 54-6544) are effective in reducing the pulmonary fibrotic outcomes of in vivo deficiency of CYB5R3 in AECIIs. Taken together, these results show that CYB5R3 in AECIIs is required to maintain resilience after lung injury and fibrosis and that therapeutic manipulation of the sGC redox state could provide a basis for treating fibrotic conditions in the lung and beyond.

Facet Dependence of Biosynthesis of Vivianite from Iron Oxides by Geobacter sulfurreducens.

Vivianite plays an important role in alleviating the phosphorus crisis and phosphorus pollution. The dissimilatory iron reduction has been found to trigger the biosynthesis of vivianite in soil environments, but the mechanism behind this remains largely unexplored. Herein, by regulating the crystal surfaces of iron oxides, we explored the influence of different crystal surface structures on the synthesis of vivianite driven by microbial dissimilatory iron reduction. The results showed that different crystal faces significantly affect the reduction and dissolution of iron oxides by microorganisms and the subsequent formation of vivianite. In general, goethite is more easily reduced by Geobacter sulfurreducens than hematite. Compared with Hem_{100} and Goe_L{110}, Hem_{001} and Goe_H{110} have higher initial reduction rates (approximately 2.25 and 1.5 times, respectively) and final Fe(II) content (approximately 1.56 and 1.20 times, respectively). In addition, in the presence of sufficient PO43-, Fe(II) combined to produce phosphorus crystal products. The final phosphorus recoveries of Hem_{001} and Goe_H{110} systems were about 5.2 and 13.6%, which were 1.3 and 1.6 times of those of Hem_{100} and Goe_L{110}, respectively. Material characterization analyses indicated that these phosphorous crystal products are vivianite and that different iron oxide crystal surfaces significantly affected the size of the vivianite crystals. This study demonstrates that different crystal faces can affect the biological reduction dissolution of iron oxides and the secondary biological mineralization process driven by dissimilatory iron reduction.

The effect of different carbon reductants on the production of ferrosilicon 75% on an industrial scale in an electric arc furnace

Ferrosilicon production is based on the carbothermal reduction of silica and iron oxide in submerged electric arc furnaces. The reducing process of iron oxide and silicon oxide is carried out by the carbon contained in carbon materials such as coal, charcoal, semi-coke, and all types of coke. Based on its inherent and functional characteristics, the kind of carbon material can be effective in the ferrosilicon production process and furnace energy consumption. Therefore, in this work, which was performed by Iran Ferrosilice company, in a long period of 5 years, the effects of seven combinations of different carbon materials on the electrical and metallurgical performance of the process were investigated. The results showed that the minimum value of energy coefficient per ton (8.46 MWh/ton) was obtained using combination 5 (consisting of 55% coal, 30% semi-coke, 5% charcoal, and wood chips). The use of wood chips reduced the energy consumption by 3.03 MWh/ton. The composition consisting of 50% coal, 35% semi-coke, 15% charcoal, and wood chips had the highest Si% of 73.64% and the lowest Al% of 1.54%. Finally, by evaluating all the results, especially the reduction of energy consumption and recovery of Si, compound 5 was introduced as the optimal compound in the ferrosilicon production process.

Green synthesis of sodalite-derived hybrid as iron redox mediator for excellent photo-fenton like reaction

The sluggish kinetics of Fe(II) regeneration and inactive Fe(III) sludge accumulation strongly hampers the scientific progress of Fenton-related reactions toward practical application. Herein, we developed a durable zero-valent iron super dispersed sodalite-graphene oxide hybrid (Z@GO-SOD) via reactive oxidation species (ROSs) route using industrial waste lithium silicon fume (LSF) as raw material, and first applied it as a visible-light-driven photocatalyst to initiate Fenton-like reaction for effective ciprofloxacin (CIP) remediation. The Z@GO-SOD featured a mesoporous structure with iron strongly interaction with GO hybrid zeolite, the GO hybrid zeolite acted as an efficient mediator, facilitating charge separation and transportation to expedite the iron redox cycle. The presence of persulfate could further act as an electron acceptor to boost photogenerated e−/h+ separation, resulting in more OH for fast CIP removal. Over 90 % of CIP was removed within 30 min in the Z@GO-SOD/Vis/PS system with the usage of merely 0.4 g/L catalyst, and as high as 71% CIP was completely mineralized, which outperformed most of the state-of-the-art photo-Fenton catalysts. Meanwhile, Z@GO-SOD also demonstrated excellent reusability and stability. This work indicated the feasibility of utilizing solar energy for both preparation of catalyst and remediation of wastewater, paying the way for a sustainable solution for environmental solid waste pollution and water scarcity issue.

Improving the efficiency of steelmaking slag processing at PJSC “MMK”

This paper assesses the efficiency of metallurgical slag processing at PJSC “MMK” in LLC “Slagservice”, which indicates the need to improve it in terms of increasing the degree of extraction of iron from slag. Proposals for improving the existing technology of steelmaking slag processing and the development of new technologies have been developed. An assessment of the efficiency of the metallurgical slag recycling at LLC “Slakservice” in 2019 is given. Ways to improve the efficiency of steelmaking slag processing in the conditions of existing production are presented. The description of the experimental setup for testing the basic principles of the proposed technology is given. The method of metallurgical slag processing was used in laboratory conditions, it corresponds to the existing technology of metallurgical slag processing in LLC “Slakservice”, including slag crushing, classification by size, metal separation by screening and magnetic separation.It is established that the method of separation of slag-metal conglomerate can be used in industrial conditions. The method of assessing the efficiency of metallurgical slag processing through the degree of extraction of metal-containing components from the slag was used for processing the results. A method of improving the existing technology of steelmaking slag processing is proposed, which includes increasing the content of metallic iron in the current converter slag by means of liquid-phase reduction of iron oxides using coal. The method of increasing the content of metallic iron in the current BOF slag in slag bowls using movable reactors is proposed. This method makes it possible to increase the content of metallic iron in the current BOF slag by about two times, which contributes to increasing the efficiency of magnetic separation at the stage of secondary slag processing.

Synergistic adsorption and oxidation of trivalent antimony from groundwater using biochar supported magnesium ferrite: Performances and mechanisms

Antimony (Sb) pollution is considered an environmental problem, since Sb is toxic and carcinogenic to humans. Here, a novel biochar supported magnesium ferrite (BC@MF) was adopted for Sb(III) removal from groundwater. The maximum adsorption capacity was 77.44 mg g−1. Together with characterization, batch experiments, kinetics, isotherms, and thermodynamic analyses suggested that inner-sphere complexation, H–bonding, and electrostatic interactions were the primary mechanisms. C–C/CC, C–O, and O–CO groups and Fe/Mg oxides might have acted as adsorption sites. The adsorbed Sb(III) was oxidized to Sb(V). The generation of reactive oxygen species, iron redox reaction, and oxidizing functional groups all contributed to Sb(III) oxidation. Furthermore, the fixed-bed column system demonstrated a satisfactory Sb removal performance; BC@MF could treat ∼6060 BV of simulated Sb-polluted groundwater. This research provides a promising approach to sufficiently remove Sb(III) from contaminated groundwater, providing new insights for the development of innovative strategies for heavy metal removal.