Iron Oxide Research Articles

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

Active Targeting Hyaluronan Conjugated Nanoprobe for Magnetic Particle Imaging and Near-Infrared Fluorescence Imaging of Breast Cancer and Lung Metastasis.

A major contributing cause to breast cancer related death is metastasis. Moreover, breast cancer metastasis often shows little symptoms until a large area of the organs is occupied by metastatic cancer cells. Breast cancer multimodal imaging is attractive since it integrates advantages from several modalities, enabling more accurate cancer detection. Glycoprotein CD44 is overexpressed on most breast cancer cells and is the primary cell surface receptor for hyaluronan (HA). To facilitate breast cancer diagnosis, we report an indocyanine green (ICG) and HA conjugated iron oxide nanoparticle (NP-ICG-HA), which enabled active targeting to breast cancer by HA-CD44 interaction and detected metastasis with magnetic particle imaging (MPI) and near-infrared fluorescence imaging (NIR-FI). When evaluated in a transgenic breast cancer mouse model, NP-ICG-HA enabled the detection of multiple breast tumors in MPI and NIR-FI, providing more comprehensive images and a diagnosis of breast cancer. Furthermore, NP-ICG-HAs were evaluated in a lung metastasis model. Upon NP-ICG-HA administration, MPI showed clear signals in the lungs, indicating the tumor sites. This is the first time that HA-based NPs have enabled MPI of cancer. NP-ICG-HAs are an attractive platform for noninvasive detection of primary breast cancer and lung metastasis.

Controllable Synthesis of Fe2O3/Nickel Cobaltite Electrocatalyst to Enhance Oxidation of Small Molecules

Nickel-based catalysts have been widely recognized as highly promising electrocatalysts for oxidation. Herein, we designed a catalyst surface based on iron oxide electrodeposited on NiCo2O4 spinel oxide. Nickel foam was used as a support for the prepared catalysts. The modified surface was characterized by different techniques like electron microscopy and X-ray photon spectroscopy. The activity of the modified surface was investigated through the electrochemical oxidation of different organic molecules such as urea, ethanol, and ethylene glycol. Therefore, the modified Fe@ NiCo2O4/NF current in 1.0 M NaOH and 1.0 M fuel concentrations reached 31.4, 27.1, and 17.8 mA cm−2 for urea, ethanol, and ethylene glycol, respectively. Moreover, a range of kinetic characteristics parameters were computed, such as the diffusion coefficient, Tafel slope, and transfer coefficient. Chronoamperometry was employed to assess the electrode’s resistance to long-term oxidation. Consequently, the electrode’s activity exhibited a reduction ranging from 17% to 30% over a continuous oxidation period of 300 min.

Effect of calcination temperature on structure evolution of hematite nanoparticles

The objective of this study is to investigate the transition structure of iron oxide, specifically the change from magnetite to hematite, as well as the influence of calcination temperature on the structural growth of hematite nanoparticles. The magnetite was extracted from the native iron sand in Indonesia using the coprecipitation procedure. To generate hematite, magnetite was calcined at various temperatures (350, 500, 650, and 800 °C). The structural changes resulting from the effect of calcination temperature were investigated by combining a number of characterisation methods. The crystal structure was examined using synchrotron x-ray diffraction (SRD) and the local structure was examined using x-ray absorption spectroscopy (XAS). Crystallite size was calculated using the Debye-Schrerrer equation at the most dominant SRD peak. Surface morphology was investigated using scanning electron microscopy (SEM). SRD data revealed that the sample calcined at 350 °C displayed both the Fe3O4 and α-Fe2O3 phases, while higher temperatures revealed the single-phase α-Fe2O3. Furthermore, an increase in calcination temperature was shown to be associated with an increase in crystallinity and crystallite size. For the samples H350 and H800, the crystallinity increased from 95.56 to 98.17%. In the magnetite, H350, H500, H650, and H800 samples, the crystallite size increased from 9.57 to 29.55, 16.40, 28,48, 29.26, and 29.55 nm. Higher calcination temperatures, on the other hand, increase the interatomic distance while decreasing the Debye–Waller factor, according to XAS fitting data. It can be inferred that around 500 °C, the transition from Fe3O4 to single-phase α-Fe2O3 was observed. While a greater calcination temperature of at least 800 °C would alter the structural parameters, it would not affect the phase.

Evaluation of Pigment-Modified Clear Binders and Asphalts: An Approach towards Sustainable, Heat Harvesting, and Non-Black Pavements

Pavement construction practices have evolved due to increasing environmental impact and urban heat island (UHI) effects, as pavements, covering over 30% of urban areas, contribute to elevated air temperatures. This study introduces heat-reflective pavements, by replacing conventional black bitumen with a clear binder and pigment-modified clear binders. Titanium dioxide white, zinc ferrite yellow, and iron oxide red pigments are used to give asphalt corresponding shades. The asphalt and bitumen specimens were subjected to thermal analysis in heat sinks, under varying solar fluxes. The pigment dosage was maintained at 4%, according to the weight of the total mix, for all pigment types. The samples were heated and cooled for 3 h and 2 h, respectively. Mechanical testing was conducted to ascertain the impact of temperature variations on both the neat clear binder (C.B) and pigmented C.B and asphalt mixture samples. Wheel tracking and dynamic modulus tests were conducted to evaluate their performance under high temperatures. The results indicate that non-black asphalt mixtures exhibit significant temperature reductions, up to 9 °C, which are further enhanced by pigmented binders, up to 11 °C. It was found that asphalt with a clear or transparent binder demonstrated lower temperatures and faster heat dissipation in extreme conditions. Moreover, C.B asphalt mixtures displayed a rut resistance of 15%, with the pigmented C.B asphalt mixture showing a remarkable rut resistance of 73%, outperforming conventional asphalt. Non-black mixtures, especially C.B + zinc ferrite, showed improved resistance to permanent deformation in dynamic modulus tests.

Oxidation Behaviour of Fe-28Al-5Si at.% Alloyed with Ti and Mo

AbstractThe high-temperature oxidation behaviour of Fe-28Al-5Si, Fe-28Al-5Si-2Mo and Fe-28Al-5Si-2Ti (in at.%) was investigated. Cyclic oxidation tests of iron aluminides were performed at 900°C and 1100°C. The oxidation kinetics and oxidation behaviour (by measuring of total weight gain, etc.) were described. The structure of the alloys’ surfaces after oxidation, as well as the composition and morphology of oxide layers, was analysed by optical microscopy, scanning electron microscopy, SEM–EDS and X-ray diffraction. The beneficial effect of alloying with titanium or molybdenum on the oxidation resistance of Fe-Al-Si-based alloys was observed at temperatures of 900°C and 1100°C. Titanium and molybdenum suppress the formation of eutectic regions of the secondary phase in the structure, which preferentially oxidize. Therefore, a thin and compact alumina layer (only minor amounts of iron oxides and ZrO2) formed on the surface of Fe-28Al-5Si-2Mo and Fe-28Al-5Si-2Ti at 900°C. These alloys maintain low weight gains even at a temperature of 1100°C. On the other hand, alloy Fe-28Al-5Si contains a high number of eutectics-like areas, which causes ingress of the oxidation (selective oxidation of eutectic areas) and breakaway oxidation is observed at 900°C and 1100°C, respectively.