Iron Oxide Research Articles

Size, polyglycerol grafting, and net surface charge of iron oxide nanoparticles determine their interaction and toxicity in Caenorhabditis elegans

The widespread application of engineered nanoparticles (NPs) in environmental remediation has raised public concerns about their toxicity to aquatic organisms. Although appropriate surface modification can mitigate the ecotoxicity of NPs, the lack of polymer coating to inhibit toxicity completely and the insufficient knowledge about charge effect hinder the development of safe nanomaterials. Herein, we explored the potential of polyglycerol (PG) functionalization in alleviating the environmental risks of NPs. Iron oxide NPs (ION) of 20, 100, and 200 nm sizes (IONS, IONM and IONL, respectively) were grafted with PG to afford ION-PG. We examined the interaction of ION and ION-PG with Caenorhabditis elegans (C. elegans) and found that PG suppressed non-specific interaction of ION with C. elegans to reduce their accumulation and to inhibit their translocation. Particularly, IONS-PG was completely excluded from worms of all developmental stages. By covalently introducing sulfate, carboxyl and amino groups onto IONS-PG, we further demonstrated that positively charged IONS-PG-NH3+ induced high intestinal accumulation, cuticle adhesion and distal translocation, whereas the negatively charged IONS-PG-OSO3– and IONS-PG-COO– were excreted out. Consequently, no apparent deleterious effects on brood size and life span were observed in worms treated by IONS-PG and IONS-PG bearing negatively charged groups. This study presents new surface functionalization approaches for developing ecofriendly nanomaterials.

Sodium salt promoted the generation of nano zero valent iron by carbothermal reduction: For activating peroxydisulfate to degrade antibiotic

Carbothermal reduction is a promising method for the industrial preparation of nano-zero-valent iron. Preparing it also involves very high pyrolysis temperatures, which leads to a significant amount of energy consumption. The temperature required for the preparation of nano-zero-valent iron by carbothermal reduction was reduced by 200 °C by the addition of sodium salt. Carbon-loaded nano zero-valent iron (Fe0/CB-Na) was prepared by carbothermal reduction through the addition of sodium salt. The results showed that Fe0/CB-Na@700 had the same activation performance as Fe0/CB@900 and the newly prepared nano-zero-valent iron. The addition of sodium salt promoted the transfer of oxygen from the iron oxide to the carbon structure during the roasting process so that the iron oxide was reduced to as much Fe0 as possible. Thus, sodium salts were optimized for the preparation of nano-zero-valent iron by carbothermal reduction through interfacial amorphization and oxygen transfer, thus reducing the preparation cost.

Investigation of borate glasses reinforced with iron (III) oxide [Fe2O3]: Preparation, physical, UV–Vis properties and γ-ray attenuation efficacy

Five samples of borate glasses reinforced with various ratios of Fe3+ ions with chemical formula (60-X)B2O3–10ZnO–10CdO–5Li2O–15Na2O-XFe2O3: (0.0 (Fe-0.0) ≤ X ≤ 1 (Fe-1.0) mol%) were prepared using the melt-quenching technique. The structure, physical, optical characteristics, and γ-ray attenuation properties of the prepared Fe-X glasses have been investigated. The amorphous state of Fe-X glasses confirmed by XRD observations. Density (ρglass) of the Fe-X glasses increased from 3.21 g cm−3 to 3.91 g cm−3. Molar volume (Vm) gradually reduced from 18.87 cm3/mol to 15.35 cm3/mol with increasing Fe2O3 content in the glass network from 0.0 to 1.0 mol%. The color of Fe-X glasses changed from yellow to brown according to the absorption bands located at around 385–412 nm and 407–429 nm within the visible spectrum. The indirect optical band gap (Eg) decreased from 3.37 eV to 2.78 eV, while the linear refractive index (no) increased from 2.31 to 2.45. Mass- (MAC) and linear- (LAC) attenuation coefficients increased as Fe3+ ions increased in the glass network. The Fe-1.0 sample with highest Fe2O3 content possessed the lowest values of half-value layer (HVL) and mean free path (MFP) shielding parameters. Results revealed that the suggested glass compositions can be applied in optical and radiation protection fields.

Hyperthermia/glutathione-triggered ferritin nanoparticles amplify the ferroptosis for synergistic tumor therapy

Breast cancer is the most diagnosed malignancy in women globally, and drug resistance is among the major obstacles to effective breast cancer treatment. Emerging evidence indicates that photothermal therapy and ferroptosis are both promising therapeutic techniques for the treatment of drug-resistant breast tumors. In this study, we proposed a thermal/ferroptosis/magnetic resonance imaging (MRI) triple functional nanoparticle (I@P-ss-FRT) in which ferritin, an iron storage material with excellent cellular uptake capacity, was attached via disulfide bonds onto polydopamine coated iron oxide nanoparticle (I@P) as photothermal transduction agent and MRI probe. I@P-ss-FRT converted the near-infrared light (NIR) into localized heat which accelerated the release of ferrous ions from ferritin accomplished by glutathione reduction and subsequently induced ferroptosis. The drug-resistant cancer cell lines exhibited a more significant uptake of I@P-ss-FRT and sensitivity to PTT/ferroptosis compared with normal cancer cell lines. In vivo, I@P-ss-FRT plus NIR displayed the best tumor-killing potential with inhibitory rate of 83.46%, along with a decline in GSH/GPX-4 content and an increase in lipid peroxides generation at tumor sites. Therefore, I@P-ss-FRT can be applied to combat drug-resistant breast cancer.

HSA, free Radicals, and antibacterial interaction with ferrous oxide nanoparticles synthesized from Amorphophallus paeoniifolius

This work provides a sustainable method for producing iron oxide nanoparticles (FeONPs) using an extract from Amorphophallus paeoniifolius (AP) tubers. The nanoparticles were then thoroughly characterized by TGA/DSC, UV, FTIR, and SEM examination. They demonstrated their strong antibacterial properties against Gram-positive and Gram-negative microbes. The sizes of the ZOI were found to be 19, 25, 16 and 14 at 100 mg/mL as compared to cefoxitin as 18, 23, 8 and 12 mm for Pseudomonas aeruginosa (P. aeruginosa), Escherichia coli (E. coli), Bacillus subtilis (B. subtils) and Staphylococcus aureus (S. aureus) respectively. Their interaction with 2,2-diphenylpicrylhydrazyl (DPPH) revealed their free radical scavenging up to 70 %. NPs at 260 nm (λmax) have shown a hypo-chromic effect in the spectrophotometric approach, suggesting that FeONPs are intercalating in nature. The fluorescence quenching tests indicated the development of a non-fluorescent complex, implying FeONPs interaction with human serum albumin (HSA). As per Scatchard parameters, five binding sites observed in HSA during the interaction with FeONPs, where the Kb value indicated the NPs strong binding strength. The HSA and DPPH interaction nature of FeONPs suggests that they might be helpful in medical applications.

Experimental investigation and thermodynamic analysis of application of hybrid nanofluid in a parabolic solar trough collector.

In this research, thermal modeling has been done to investigate the effect of nanofluid on the performance of the linear parabolic collector. Therminol vapor/liquid phase fluid (VP-1) has been used as a base fluid; iron oxide nanoparticles have been used to produce mono-nanofluid; and iron oxide multi-walled carbon nanotubes nanocomposite has been used as nanoparticles to produce hybrid nanofluid. The fluid flow inside the absorber tube of the collector is assumed to be turbulent. The results show that when hybrid nanofluid and mono-nanofluid are used, the energy and exergy efficiencies of the collector are higher than those for the conditions of using the base fluid, but their amount is slightly lower with the use of hybrid nanofluid than when the working fluid is mono-nanofluid. According to the obtained results, the highest energy efficiency of the linear parabolic collector using nanofluid and mono-nanofluid is 70.2% and 70.4%, respectively, and the highest exergy efficiency is 35.7% and 35.9%, respectively. Despite this, the friction coefficient of mono-nanofluid compared to hybrid nanofluid was obtained on average about 9% higher. The results showed that the criterion for evaluating the performance of the collector (hydrodynamic thermal efficiency) when hybrid nanofluid is used is more than when mono-nanofluid is used.

Cu1-Fe Dual Sites for Superior Neutral Ammonia Electrosynthesis from Nitrate.

The electrochemical nitrate reduction reaction (NO3RR) is able to convert nitrate (NO3-) into reusable ammonia (NH3), offering a green treatment and resource utilization strategy of nitrate wastewater and ammonia synthesis. The conversion of NO3- to NH3 undergoes water dissociation to generate active hydrogen atoms and nitrogen-containing intermediates hydrogenation tandemly. The two relay processes compete for the same active sites, especially under pH-neutral condition, resulting in the suboptimal efficiency and selectivity in the electrosynthesis of NH3 from NO3-. Herein, we constructed a Cu1-Fe dual-site catalyst by anchoring Cu single atoms on amorphous iron oxide shell of nanoscale zero-valent iron (nZVI) for the electrochemical NO3RR, achieving an impressive NO3- removal efficiency of 94.8% and NH3 selectivity of 99.2% under neutral pH and nitrate concentration of 50 mg L-1 NO3--N conditions, greatly surpassing the performance of nZVI counterpart. This superior performance can be attributed to the synergistic effect of enhanced NO3- adsorption on Fe sites and strengthened water activation on single-atom Cu sites, decreasing the energy barrier for the rate-determining step of *NO-to-*NOH. This work develops a novel strategy of fabricating dual-site catalysts to enhance the electrosynthesis of NH3 from NO3-, and presents an environmentally sustainable approach for neutral nitrate wastewater treatment.

Controlling the Magnetic Responsiveness of Cellulose Nanofiber Particles Embedded with Iron Oxide Nanoparticles.

2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofiber (TOCN) particles, an innovative biobased material derived from wood biomass, have garnered significant interest, particularly in the biomedical field, for their distinctive properties as biocompatible particle adsorbents. However, their microscopic size complicates their separation in liquid media, thereby impeding their application in various domains. In this study, superparamagnetic magnetite nanoparticles (NPs), specifically iron oxide Fe3O4 NPs with an average size of 15 nm, were used to enhance the collection efficiency of TOCN-Fe3O4 composite particles synthesized through spray drying. These composite particles exhibited a remarkable ζ-potential (approximately -50 mV), indicating their high stability in water, as well as impressive magnetization properties (up to 47 emu/g), and rapid magnetic responsiveness within 60 s in water (3 wt % Fe3O4 to TOCN, 1 T magnet). Furthermore, the influence of Fe3O4 NP concentrations on the measurement of the speed of magnetic separation was quantitatively discussed. Additionally, the binding affinity of the synthesized particles for proteins was assessed on a streptavidin-biotin binding system, offering crucial insights into their binding capabilities with specific proteins and underscoring their significant potential as functionalized biomedical materials.

Efficient Strategy to Synthesize Tunable pH-Responsive Hybrid Micelles Based on Iron Oxide and Gold Nanoparticles.

The preparation of multifunctional nanomaterials based on inorganic nanoparticles with organic materials has emerged as a promising strategy for the development of new nanomedicines for in vitro and in vivo biomedical applications. Here, we synthesized pH-responsive hybrid inorganic micelles by combining a novel pH-responsive amphiphilic molecule with hydrophobic payloads. This amphiphile was synthesized in a one-pot reaction and self-assembled readily into micelles under acidic pH conditions. In the presence of hydrophobic NP payloads such as AuNPs or IONPs, the amphiphile self-organized around them through hydrophobic interactions, resulting in the formation of colloidally stable hybrid micelles. The size of the hydrophobic NPs determined the pH-response of the inorganic hybrid micelles, which is tuned from pH 7 to 11 for our pH-responsive amphiphilic molecule. This achievement represents a novel approach for the synthesis of tunable pH-responsive hybrid micelles based on inorganic NPs for biomedical imaging, hyperthermia treatment, and also drug delivery nanosystems.

Irradiation-assisted synthesis of smart hydrogels based on nanomagnetic semi-interpenetrating p(HEMA)/PVP networks for the cleaning of cultural heritage artifacts

Preservation of our cultural and historical heritage as a testimony to our shared past is a responsibility that demands significant attention. One of the most critical and delicate aspects of conserving such treasures is cleaning them safely and effectively. Chemical hydrogels specifically designed for cleaning cultural heritage artifacts allow for the containment and controlled release of water. Based on a generic approach, a smart nanomagnetic hydrogel was developed using a semi-interpenetrating polymer network (semi-IPN) of polyhydroxyethyl methacrylate (p(HEMA)) and polyvinyl pyrrolidone (PVP). Gamma irradiation was employed to perform simultaneous in-situ polymerization, crosslinking, and also immobilization of iron oxide magnetic nanoparticles (MNPs). The chemical and structural characteristics of the nanomagnetic hydrogel were investigated using gel content, equilibrium water content, field-emission scanning electron microscopy, magnetic properties, compressive strength, dehydration kinetics, and adhesion tests. The optimal formula for smart hydrogel was a ratio of monomer to polymer 50:50, a water content of 60 wt.%, a gamma radiation dose of 20 kGy, and 3 wt.% of MNP. Two cotton canvas case studies demonstrate the versatility and effectiveness of the selected hydrogel in removing dirt and confining the water-based cleaning system. It was found that no color leaching occurred during the cleaning process.

Enhancing anaerobic digestion of actual papermaking wastewater with addition of Fenton sludge

The effect of Fenton sludge on anaerobic digestion of actual papermaking wastewater was investigated in this study. The results showed the iron in the Fenton sludge primarily exists in the form of needle-like iron oxide (FeOOH) and showed high electron transfer capability. Fenton sludge promoted electron transport in anaerobic digestion and electron transport system activity increased by 59 %. Fenton sludge enhanced the metabolic activity of anaerobic microorganisms, especially that of the hydrogenotrophic methanogens, the content of coenzyme F420 increased by 48.9 %. Besides, the microbial community structure in anaerobic digestion was affected by Fenton sludge, the quantity of microorganisms increased significantly. The dissimilatory iron-reducing bacteria (Desulfobacterota) and hydrogenotrophic methanogens (Methanobacterium and Methanolinea) were enriched, which promoted the methane production. As a result, the anaerobic digestion performance of papermaking wastewater was promoted significantly by adding Fenton sludge, the organic matter removal efficiency and methane production increased by 11.17 % and 15.12 %. This study provided an effective solution for the optimisation of anaerobic treatment of actual refractory organic wastewater.

Advanced Electrode Materials based on Brownmillerite Calcium Ferrite for Li‐ion Batteries

Iron‐based materials are considered potential anode materials for lithium‐ion batteries thanks to their low cost, abundancy, non‐flammability, good safety, environmental benignity, and high specific capacity. Here, a series of calcium iron oxides materials having brownmillerite structure (i.e., Ca2Fe2‐xMxO5, where M=Mn, Ni and Cu and x=0 and 0.1) has been extensively studied for their use as conversion anodes in lithium cell. In particular, a mechanochemical approach has been used either to synthesize the samples and to prepare electrodes for the tests in lithium cell. Ca2Fe2O5 based electrodes proved excellent performance in lithium cell, approaching the theoretical capacity and being stable upon prolonged cycling (529 mAh g‐1 at C/10 and a capacity retention of 81 % after 100 cycles). Through the use of ex‐situ diffraction measurements, we have analyzed the conversion mechanism and proved the partial reversibility of its electrochemical reaction. Also, the incorporation of dopants into the structure of calcium iron oxide resulted in further improvement of its electrochemical performance as is the case of Mn doped sample that show a considerable specific capacity of 567 mAh g‐1 and the capacity retention is almost 99 % after 100 cycles.

Investigation of silica coated iron oxide nanoparticles and activated carbon as a potential fluid loss additive and Pakistan shale inhibitor in water-based mud system coupled with advance image processing technique

Investigation of silica coated iron oxide nanoparticles and activated carbon as a potential fluid loss additive and Pakistan shale inhibitor in water-based mud system coupled with advance image processing technique

Innovative Agrowaste Banana Peel Extract-Based Magnetic Iron Oxide Nanoparticles for Eco-Friendly Oxidative Shield and Freshness Fortification

AbstractThis study presents the synthesis of agro-waste banana peel extract-based magnetic iron oxide nanoparticles (BPEx-MIONPs), emphasizing antioxidant capacity and food preservation. Using iron (III) chloride hexahydrate (FeCl3 · 6 H2O) as a precursor and a reducing agent from agro-waste peel extract, a precisely controlled process yielded BPEx-MIONPs. Characterization involved X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR). XRD revealed tetragonal Fe2O3, cubic magnetite structure, and monoclinic FexOy-NPs with an average size of 14.8 nm. TEM and SEM revealed diverse morphologies. TEM displayed both spherical and elongated nanoparticles, with some appearing as thin fibrils. In contrast, SEM images depicted an array primarily consisting of spherical nanoparticles, resembling coral reef formations. FTIR confirmed Fe–O bonds (1000 –400 cm-1). The antioxidant assessment showed robust DPPH free radical scavenging; BPEx achieved 100% inhibition at 18 min, and BPEx-MIONPs had an IC50 of ~ 136 µg/mL. BPEx-MIONPs, stabilized with banana-based bioplastic, effectively preserved grapes, reducing weight loss to 6.2% on day 3, compared to the control (19.0%). This pioneering study combines banana peel antioxidants with magnetic iron oxide nanoparticles, providing sustainable solutions for food preservation and nano-packaging. Ongoing research aims to refine conditions and explore broader applications of BPEx-MIONPs. Graphical Abstract

Enhancing iron biogeochemical cycling for canga ecosystem restoration: insights from microbial stimuli

IntroductionThe microbial-induced restoration of ferruginous crusts (canga), which partially cover iron deposits and host unique ecosystems, is a promising alternative for reducing the environmental impacts of the iron mining industry.MethodsTo investigate the potential of microbial action to accelerate the reduction and oxidation of iron in substrates rich in hematite and goethite, four different microbial treatments (water only as a control − W; culture medium only − MO; medium + microbial consortium − MI; medium + microbial consortium + soluble iron − MIC) were periodically applied to induce iron dissolution and subsequent precipitation. Except for W, all the treatments resulted in the formation of biocemented blocks.ResultsMO and MI treatments resulted in significant goethite dissolution, followed by precipitation of iron oxyhydroxides and an iron sulfate phase, due to iron oxidation, in addition to the preservation of microfossils. In the MIC treatment, biofilms were identified, but with few mineralogical changes in the iron-rich particles, indicating less iron cycling compared to the MO or MI treatment. Regarding microbial diversity, iron-reducing families, such as Enterobacteriaceae, were found in all microbially treated substrates.DiscussionHowever, the presence of Bacillaceae indicates the importance of fermentative bacteria in accelerating the dissolution of iron minerals. The acceleration of iron cycling was also promoted by microorganisms that couple nitrate reduction with Fe(II) oxidation. These findings demonstrate a sustainable and streamlined opportunity for restoration in mining areas.

Green Synthesis and Characterization of CuO, Fe2O3 and CuO/Fe2O3 Compounds Investigation

Green chemistry techniques are increasingly being used to produce nanomaterials from easily accessible natural resources. The present study utilized a cost-effective and environmentally sustainable method to separately synthesize copper oxide, iron oxide, and mixed oxide nanoparticles. Copper (II) nitrate trihydrate and iron (III) nitrate nonahydrate were utilized as precursors with the help of fruit peel extracts. The nano-oxides were synthesized from the local fruit peels, specifically orange, cherry, and sidra (Ziziphus jujuba), by a simple procedure that involved heating the peels with distilled water, filtration, adding precursor, and calcination. Experiments were conducted on the resultant powders to evaluate their structural, biological, and physical characteristics. The results of the X-ray diffraction analysis showed that pure crystallite structures of CuO and Fe2O3 were formed, ternary compound CuFeO2 (delafossite), and CuO / Fe2O3 (nanocomposite) were synthesized, and their purity was verified through energy dispersive X-rays (EDX). The findings from scanning electron microscopy (SEM) and particle size analysis (PSA) revealed that the nanoparticles are semi-spherical, with particle sizes ranging from 83.9 to 118.7 nm for CuO, from 95.2 to 119.8 nm for Fe2O3, and from 60.6 to 90.4 nm for mixed oxides extracted from three fruit peels. The conducted experiments on bacterial and fungal resistance revealed that the produced oxides are effective antibacterial and antifungal particles. The synthesized nanoparticles were also analysed through AFM and Toxicity.

Comparative transcriptomics revealed neurodevelopmental impairments and ferroptosis induced by extremely small iron oxide nanoparticles

Iron oxide nanoparticles are a type of nanomaterial composed of iron oxide (Fe3O4 or Fe2O3) and have a wide range of applications in magnetic resonance imaging. Compared to iron oxide nanoparticles, extremely small iron oxide nanoparticles (ESIONPs) (∼3 nm in diameter) can improve the imaging performance due to a smaller size. However, there are currently no reports on the potential toxic effects of ESIONPs on the human body. In this study, we applied ESIONPs to a zebrafish model and performed weighted gene co-expression network analysis (WGCNA) on differentially expressed genes (DEGs) in zebrafish embryos of 48 hpf, 72 hpf, 96 hpf, and 120 hpf using RNA-seq technology. The key hub genes related to neurotoxicity and ferroptosis were identified, and further experiments also demonstrated that ESIONPs impaired the neuronal and muscle development of zebrafish, and induced ferroptosis, leading to oxidative stress, cell apoptosis, and inflammatory response. Here, for the first time, we analyzed the potential toxic effects of ESIONPs through WGCNA. Our studies indicate that ESIONPs might have neurotoxicity and could induce ferroptosis, while abnormal accumulation of iron ions might increase the risk of early degenerative neurological diseases.

An Overview Analysis of Current Research Status in Iron Oxides Reduction by Hydrogen

This paper focuses on the study of current knowledge regarding the use of hydrogen as a reducing agent in the metallurgical processes of iron and steel production. This focus is driven by the need to introduce environmentally suitable energy sources and reducing agents in this sector. This theoretical study primarily examines laboratory research on the reduction of Fe-based, metal-bearing materials. The article presents a critical analysis of the reduction in iron oxides using hydrogen, highlighting the advantages and disadvantages of this method. Most experimental facilities worldwide employ their unique original methodologies, with techniques based on Thermogravimetric analysis (TGA) devices, fluidized beds, and reduction retorts being the most common. The analysis indicates that the mineralogical composition of the Fe ores used plays a crucial role in hydrogen reduction. Temperatures during hydrogen reduction typically range from 500 to 900 °C. The reaction rate and degree of reduction increase with higher temperatures, with the transformation of wüstite to iron being the slowest step. Furthermore, the analysis demonstrates that reduction of iron ore with hydrogen occurs more intensively and quickly than with carbon monoxide (CO) or a hydrogen/carbon monoxide (H2/CO) mixture in the temperature range of 500 °C to 900 °C. The study establishes that hydrogen is a superior reducing agent for iron oxides, offering rapid reduction kinetics and a higher degree of reduction compared to traditional carbon-based methods across a broad temperature range. These findings underscore hydrogen’s potential to significantly reduce greenhouse gas emissions in the steel production industry, supporting a shift towards more sustainable manufacturing practices. However, the implementation of hydrogen as a primary reducing agent in industrial settings is constrained by current technological limitations and the need for substantial infrastructural developments to support large-scale hydrogen production and utilization.

Synthesis and characterization of iron oxide nanoparticles from Lawsonia inermis and its effect on the biodegradation of crude oil hydrocarbon.

Crude oil hydrocarbons are considered major environmental pollutants and pose a significant threat to the environment and humans due to having severe carcinogenic and mutagenic effects. Bioremediation is one of the practical and promising technology that can be applied to treat the hydrocarbon-polluted environment. In this present study, rhamnolipid biosurfactant (BS) produced by Pseudomonas aeruginosa PP4 and green synthesized iron nanoparticles (G-FeNPs) from Lawsonia inermis was used to evaluate the biodegradation efficiency (BE) of crude oil. The surface analysis of G-FeNPs was carried out by using FESEM and HRTEM to confirm the size and shape. Further, the average size of the G-FeNPs was observed around 10nm by HRTEM analysis. The XRD and Raman spectra strongly confirm the presence of iron nanoparticles with their respective peaks. The BE (%) of mixed degradation system-V (PP4+BS+G-FeNPs) was obtained about 82%. FTIR spectrum confirms the presence of major functional constituents (C=O, -CH3, C-O, and OH) in the residual oil content. Overall, this study illustrates that integrated nano-based bioremediation could be an efficient approach for hydrocarbon-polluted environments. This study is the first attempt to evaluate the G-FeNPs with rhamnolipid biosurfactant on the biodegradation of crude oil.

The Prevention of Re-dissolution of Unstable Iron Oxides During the Low-Temperature Hematite Process

The Prevention of Re-dissolution of Unstable Iron Oxides During the Low-Temperature Hematite Process