Iron Oxide Research Articles

Magnetite Reduced Graphene Oxide/Ordered Mesoporous Carbon Nanocomposite as Effective Adsorbent for Removal of 2-Naphthol in Wastewater

Background: The wastewater released from various industries contains substantial amounts of organic compounds such as dyes and naphthols. However, naphthols are toxic to the environment and human health. So, it is essential to eliminate them, which will contribute to manufacturing and environmental management. Methods: In the work, an eco-friendly method is adapted to synthesize reduced graphene oxide (rGO) using Equisetum arvense plant extract as a strong reducing and stabilizing agent. Then, a hybrid nano adsorbent based on rGO and ordered mesoporous carbon (CMK-3) decorated with iron oxide nanoparticles (Fe3O4@rGO/CMK-3) was prepared as an adsorbent. We investigate the performance of Fe3O4@rGO/CMK-3 to remove 2-naphthol (2-NP). Results: The FE-SEM images exhibited spherical magnetite nanoparticles with sizes ranging from 31 to 47 nm on composite. Efficient removal (90%) of 2-NP from aqueous solution is demonstrated using high surface area Fe3O4@rGO/CMK-3 (initial concentration of 2-NP: 10 mg mL-1, pH: 5.0, time: 30 min, and amount of adsorbent dosage: 3 mg mL-1). The high surface area of Fe3O4@rGO/CMK-3, hydrogen binding, π-π stacking interaction between the benzene rings of 2-NP and graphitic skeleton of hybrid adsorbent facilitate the adsorption of 2-NP on the Fe3O4@rGO/CMK-3. The 2NP removal capacity by (Fe3O4@rGO/CMK-3) showed a significant decrease during five successive cycles. Conclusions: These results promise the potential of high surface area (Fe3O4@rGO/CMK-3) for efficient removal of 2-NP for wastewater treatment.

Modulation of Solid-state Thermal Reaction of Iron(III)Citrate by a Co-precursor Studied using Thermogravimetry: Evaluation of Kinetic and Thermodynamic Parameters and Nucleation Rate

Background:: Solid state reaction of iron(III)citrate leads to a range of ironbased oxides by varying the reaction conditions, e.g., the presence of co-precursor. The influence of reaction conditions on the kinetics of the solid-state reaction of iron(III)citrate needs to be investigated. Objective:: Kinetic analysis of the solid-state reaction of iron(III)citrate in the presence of a co-precursor has been explored to realize the influences of the co-precursor on the reaction process as well as decomposed material. Method:: Non-isothermal thermogravimetry profiles are deconvoluted to individual reaction steps. The model-free kinetic methodology is utilized to estimate step-wise activation energy and, hence, the reaction mechanism along with the reaction rate. Conversiondependent thermodynamic parameters and nucleation rate are estimated. XRD analysis has been used to characterize the decomposed material. Results:: Thermogravimetry profiles obtained for an iron(III)citrate and malonic acid mixture are deconvoluted into six steps. The decomposed nanomaterial is identified as magnetite (size 10 nm). The observed reaction mechanisms associated with each step are different, where the activation/reaction rate is conversion-dependent. A good fit between the experimental and reverse-constructed conversion profiles is obtained. The nucleation rate at higher temperatures is affected by both the extent of conversion and the heating rate. A possible reaction pathway is proposed. The study elucidates the role of malonic acid as a co-precursor in modifying the thermal reaction of iron(III)citrate and product formation. Conclusion:: This investigation proposes the applicability of suitable co-precursors as a potential controlling factor for preparing iron oxides from iron-based compounds.

Activation of Persulphate by a Waste-Extracted Metal–Organic Framework-Derived Iron Oxide as a Photocatalyst for Effective Degradation of Salicylic Acid

Activation of Persulphate by a Waste-Extracted Metal–Organic Framework-Derived Iron Oxide as a Photocatalyst for Effective Degradation of Salicylic Acid

A fused LASSO operator for fast 3D magnetic particle imaging reconstruction

Objective. Magnetic particle imaging (MPI) is a promising imaging modality that leverages the nonlinear magnetization behavior of superparamagnetic iron oxide nanoparticles to determine their concentration distribution. Previous optimization models with multiple regularization terms have been proposed to achieve high-quality MPI reconstruction, but these models often result in increased computational burden, particularly for dense gridding 3D fields of view. In order to achieve faster reconstruction speeds without compromising reconstruction quality, we have developed a novel fused LASSO operator, total sum-difference (TSD), which effectively captures the sparse and smooth priors of MPI images. Methods. Through an analysis-synthesis equivalence strategy and a constraint smoothing strategy, the TSD regularized model was solved using the fast iterative soft-thresholding algorithm (FISTA). The resulting reconstruction method, TSD-FISTA, boasts low computational complexity and quadratic convergence rate over iterations. Results. Experimental results demonstrated that TSD-FISTA required only 10% and 37% of the time to achieve comparable or superior reconstruction quality compared to commonly used fused LASSO-based alternating direction method of multipliers and Tikhonov-based algebraic reconstruction techniques, respectively. Significance. TSD-FISTA shows promise for enabling real-time 3D MPI reconstruction at high frame rates for large fields of view.

Impact of Iron Species Dispersion on Fe/ZSM‐5 Catalyst Performance for Methane Dehydroaromatization (MDA)

AbstractMethane dehydroaromatization (MDA) is one of the most promising technologies for directly transforming methane into aromatics. Unlike the extensively investigated Mo/ZSM‐5 catalysts, the structure and, consequently, the catalytic activity of Fe/ZSM‐5 are markedly influenced by the method of preparation, as shown here. In this study, we prepared 2 % and 4 % Fe/ZSM‐5 catalysts via wet impregnation (WI) and incipient wetness impregnation (IWI). Characterizations (XRD, STEM, UV‐Vis, NH3‐TPD and H2‐TPR) reveal that 2 %Fe‐WI mainly possesses isolated or low‐polymerized Fe species within zeolite channels, leading to a rapid activation and a higher benzene yield due to the faster reduction to iron suboxides under MDA conditions. In contrast, 2 %Fe‐IWI contains bulk iron oxide aggregates, resulting in a slower activation as these aggregates transform into iron carbide through successive reduction and carbonization. A deactivation kinetic study applied to the 2 % catalysts further demonstrates the quantitative relation between Fe site isolation and catalytic activity. Although both 4 % catalysts inevitably form sizable iron oxide clusters and particles due to the high Fe/Al ratio, similar trends are noted, with the WI catalysts exhibiting a shorter induction/activation period and a higher yield of benzene, paralleling observations made with 2 % catalysts.

Influence of the dietary contribution of terrestrial insects to the condition factor of bleak Alburnus alburnus in a highly polluted lowland river.

Bleak Alburnus alburnus is a highly abundant but understudied fish species, and we know little about the trophic ecology of populations inhabiting rivers in central Europe. From an ecosystem perspective, this fish species is interesting as it is known to feed on surface insects, thereby linking the terrestrial with the aquatic habitat. In a previous study, we demonstrated that this flux is intensified, and dietary contribution of terrestrial insects is higher in fish inhabiting sections of the Spree River, Germany, that are polluted from iron oxides occurring from former lignite mining activities, and thus are characterized by lower abundances of aquatic insects. As terrestrial insects can be considered as food of lower quality (measured as long-chained polyunsaturated fatty acids, n-3 LC-PUFAs) compared to aquatic prey, it is reasonable to assume that the higher contribution of terrestrial insects is related to a lower body condition in fish. In this study, we explore the trophic ecology of riverine A. alburnus and their fitness consequences of feeding on terrestrial insects. We therefore modeled a terrestrial index from stable isotopes of hydrogen (δ2H) measured in the A. alburnus muscle tissue and compared individuals caught in locations upstream of a dam that were greatly influenced by iron oxides, with individuals caught in sections located downstream of a dam where passive remediation technologies are applied. The terrestrial index was significantly higher in A. alburnus caught in locations at high-iron concentrations, characterized by low abundances of aquatic prey, compared to A. alburnus caught in unpolluted habitats at low-iron concentrations. In contradiction to our hypothesis, the terrestrial index had no significant effect on the body condition of A. alburnus (measured as Fulton's condition factor K) in the sections downstream of the dam (i.e., at low-iron concentrations) and a significant positive, albeit weak, effect in sections upstream of the dam (i.e., at high-iron concentrations). However, the condition factor was generally lower in the high-iron section, potentially related to more direct effects of the iron oxide. We conclude that in A. alburnus, terrestrial insects can be considered as the less-favored food, unless the fish occur in environments where the aquatic food is of limited availability. Further research is needed to evaluate the direct and indirect effects, including the internal n-3 LC-PUFA synthesis as an adaption toward low-quality terrestrial prey on the fitness consequences of A. alburnus.

Fast and green synthesis of iron oxide using low-power laser sintering on reduced graphene oxide sensor for ammonia gas detection

Oxide materials are important for gas sensing applications. Unfortunately, most of the synthesis methods use many toxic chemicals and need long calcination at high temperatures. Thus, developing simple and green synthesis processes, which can be performed fast and at low temperatures, is imperative for both industrial manufacturers and our environment. Here, our fast and green synthesis method based on low-power laser sintering for producing FeOx (with Fe2O3 as the main composition) is presented. Besides, FeOx particles were decorated on reduced graphene oxide (RGO) to form a resistive sensor. Notably, our FeOx material can reduce the response of RGO toward acidic gas (NO2) but it enhances the RGO response toward the basic NH3 gas. Particularly, our hybrid FeOx/RGO sensor can detect NH3 gas at above 2 ppm under dry and humidified conditions (<85 % RH). That effect of FeOx is found due to the formation of alpha-phase Fe2O3 which acts as a p-type semiconductor, which is explored and explained in the discussion section. Finally, our findings not only reveal the potential of our hybrid sensing materials for practical NH3 sensing applications but also confirm the usefulness of laser-sintering to produce catalytic oxide materials environmentally friendly and at low cost.

Genetic insights and therapeutic potential for colorectal cancer: mutation analysis of KRASgene and efficacy of Oleuropein-conjugated iron oxide nanoparticles.

This study aimed to address the challenges of treating advanced stages of colon cancer (CRC) by exploring potential therapeutic options. The research focused on the genetic aspects of CRC, specifically the mutation rate of the KRAS gene, along with other genes like TTN, APC, MUC16, and TP53, using the TCGA dataset. Additionally, the study investigated the efficacy of Oleuropein, a polyphenolic compound found in olives, in combating CRC by using iron oxide nanoparticles coated with glucose and conjugated with Oleuropein. The study characterized the physicochemical properties of the nanoparticles, and the cytotoxic effects of the nanoparticles were evaluated on CRC and normal fibroblast cell lines, demonstrating significantly higher cytotoxicity against CRC cells compared to normal cells. Furthermore, the study analyzed gene expression changes using the GSE124627 dataset to understand the influence of KRAS alterations. It identified numerous upregulated and downregulated genes in KRAS-overexpressing samples, suggesting their involvement in critical cancer-related pathways. These findings suggest that KRAS-influenced genes could serve as potential therapeutic targets for CRC treatment. The study also examined the expression levels of identified genes in CRC samples compared to normal samples. Among the upregulated genes, 22 showed significant increases in cancer samples, while 14 downregulated genes exhibited decreased expression in both KRAS-influenced and cancer samples. Cox regression analysis identified specific upregulated genes, including ANKZF1, SNAI1, PPFIA4, SIX4, and NOTUM, associated with poor prognosis. Kaplan-Meier analysis further confirmed the correlation between increased expression of these genes and higher patient mortality rates. In conclusion, this study provided valuable insights into the genetic aspects of CRC and potential therapeutic strategies. The use of Oleuropein-conjugated iron oxide nanoparticles showed promising cytotoxic effects on colon cancer cells. These findings contribute to advancing our understanding of CRC and offer potential targets for further investigation and the development of novel therapeutic approaches.

Phosphorus recycling by mineral-catalyzed ribonucleotide cleavage on iron and manganese oxides

AbstractPhosphorus is an essential element influencing both food security via plant fertilization, and water pollution through excessive phosphorus use, yet the phosphorus cycle in ecosystems is poorly known. In particular, beyond adsorption, the role of iron and manganese oxides in catalyzing the abiotic dephosphorylation of biomolecules is debated. Here, we studied the reactions of ribonucleotides, containing different phosphate bonding, with goethite, hematite, and birnessite. We employed both high-resolution mass spectrometry of solution species and molecular modeling simulations of ribonucleotide-mineral complexes. Results disclose an up to fivefold preferential hydrolytic cleavage of a phosphoanhydride bond over a phosphoester bond, indicating that mineral-catalyzed reactions reflect the hierarchy reported for the activity of phosphatase enzymes. The fourfold higher catalytic reactivity of goethite and birnessite versus hematite is explained by mineral-specific binding rather than surface area differences. Corresponding simulated adsorbate conformations at the water–mineral interfaces are proposed. Overall, our findings provide new insights on the catalytic recycling of organic phosphorus species by mineral oxides.

Facile synthesis of iron nanoparticles from Camellia Sinensis leaves catalysed for biodiesel synthesis from Azolla filiculoides

Recent years have seen an increase in research on biodiesel, an environmentally benign and renewable fuel alternative for traditional fossil fuels. Biodiesel might become more cost-effective and competitive with diesel if a solid heterogeneous catalyst is used in its production. One way to make biodiesel more affordable and competitive with diesel is to employ a solid heterogeneous catalyst in its manufacturing. Based on X-ray diffraction (XRD) and Fourier Transform infrared spectroscopy (FTIR), the researchers in this study proved their hypothesis that iron oxide core–shell nanoparticles were generated during the green synthesis of iron-based nanoparticles (FeNPs) from Camellia Sinensis leaves. The fabrication of spherical iron nanoparticles was successfully confirmed using scanning electron microscopy (SEM). As a heterogeneous catalyst, the synthesised catalyst has shown potential in facilitating the conversion of algae oil into biodiesel. With the optimal parameters (0.5 weight percent catalytic load, 1:6 oil—methanol ratio, 60 °C reaction temperature, and 1 h and 30 min reaction duration), a 93.33% yield was attained. This may be due to its acid–base property, chemical stability, stronger metal support interaction. Furthermore, the catalyst was employed for transesterification reactions five times after regeneration with n-hexane washing followed by calcination at 650 °C for 3 h.

Characterization, Dielectric Analysis and Thermal Properties of Novel Flexible Polymer Composite Films

In this work, mixtures of polypyrrole (PPy) and iron oxide (Fe2O3) are synthesized using oxidative chemical polymerization process to create a novel flexible PET/(PPy-Fe2O3) composite films. The films were characterized by different methods as FTIR, SEM, XRD and TGA to prove the efficient manufacturing of the composite. The dielectric performance measurements were done at frequency of 20 Hz to 6 MHz for the polymer PET and the composite (PPy-Fe2O3)/PET with varying concentrations of Fe2O3. Moreover, to reveal the characteristics of the fabricated composite, the contact angle, the work of adhesion, surface energy of the composite PET/(PPy-Fe2O3) films were considerably determined. The SEM results support the deposition of PPy-Fe2O3 composite on the PET surface. The water contact angle drops from 78.32° for PET to 40.11° for PET/6%(PPy-Fe2O3), while the dispersive free energy raised from 23.9 mJ m−2 to 43.7 mJ m−2and the polar free energy rises from 8.9 mJ m−2 to 22.3 mJ m−2. The concentration of Fe2O3 increased the surface features of the samples, according to the obtained results. At frequency of 100 Hz, the dielectric constant enhanced from 18 for PET to 923 for the PET/6%(PPy-Fe2O3), and the dielectric loss improved from 24 to 9231, while the energy density improved fromm 7.9 × 10−5 J/m3 for PET to 408 × 10−5 J m−3. The TGA results show marginal modifications in thermal stability after deposition the PPy/Fe2O3 on the PET film. The obtained data showed the dielectric characteristics of the PET/(PPy-Fe2O3) were improved respect to polymer PET, to can be applied the fabricated composite in storage devices and capacitors.

Facile controllable sequential electrochemical in-situ synthesis of Fe3O4/PPY hybrid electrode for supercapacitor

In this work, a facile sequential electrochemical synthesis strategy is employed for the precisely controlled in situ polymerization of pyrrole on an iron oxide substrate in the oxalic acid system. The use of porous iron oxide as a template allows for the modification of polypyrrole to create a large conductive network while preserving the integrity of the substrate. This process improves the poor conductivity of conventional metal oxides, allowing for the synthesis of a Fe3O4/PPY hybrid electrode material. The experiments elucidated the mechanism of pyrrole surface morphology coupled with the deposition amount threshold affecting the electrode performance. This was achieved by elucidating the regulation laws of key deposition process parameters (pyrrole monomer concentration, scanning rate, and number of cycles) on the diffusion and oxidation behaviors of pyrrole during the continuous polymerization process. Furthermore, the electrochemical behaviors of the Fe3O4/PPY hybrid electrode were better resolved. The results demonstrate that the deposition amount of PPY on the Fe3O4/PPY hybrid electrode material is within the optimized threshold (1 × 10−6∼3 × 10−6 g), exhibiting a regular and uniform surface morphology with no agglomeration, which indicates a competitive specific capacitance (215.12 mF cm−2 at 1.1 mA cm−2). This strategy of structure-modulated synergistic functional hybridization offers a new approach for designing efficient binder-free hybridized electrode materials.

Biocompatible Cobalt Oxide Nanoparticles for X-ray Fluorescence Microscopy.

The synthesis of water-soluble nanoparticles is a well-developed field for ferrite-based nanoparticles with the majority consisting of iron oxide or mixed metal iron oxide nanoparticles. However, the synthesis of non-agglomerated non-ferrite metal/metal oxide NPs is not as well established. The synthesis and characterization of uniform 20 nm, biologically compatible cobalt oxide (CoO) nanoparticles (NPs) is described. These nanoparticles have two principle components: 1) a CoO core of suitable size to contain enough cobalt atoms to be visualized by X-ray fluorescence microscopy (XFM) and 2) a robust coating that inhibits NP aggregation as well as renders them water-soluble and biocompatible (i.e. stealth coatings). Stable cobalt oxide NPs are obtained with octadecyl amine coatings as reported by Bhattacharjee. Two strategies for solubilizing these NPs in water were investigated with varying degrees of success. Exchanging the octadecyl amine coating for a nitrodopamine anchored PEG coating yielded the desired water-soluble NPs but in very low yield. Alternately, leaving the octadecyl amine coating on the NP and interdigitating this with a maleic anhydride-vinyl copolymer with different hydrophobic sidechains followed by opening the maleic anhydride ring with amine substituted PEG polymers (the water solubilizing component), yielded the desired water soluble NPS were obtained in good yield. Characterization data for the nanoparticles and the components of the coatings required for bioorthogonal reactions to ligate them with biotargeting agents are also described.

Adsorption Behavior of Co2+, Ni2+, Sr2+, Cs+, and I- by Corrosion Products α-FeOOH from Typical Metal Tanks.

Throughout the nuclear power production process, the disposal of radioactive waste has consistently raised concerns about environmental safety. When the metal tanks used for waste disposal are corroded, radionuclides seep into the groundwater environment and eventually into the biosphere, causing significant damage to the environment. Hence, investigating the adsorption behavior of radionuclides on the corrosion products of metal tanks used for waste disposal is an essential component of safety and evaluation protocols at disposal sites. In order to understand the adsorption behavior of important radionuclides 60Co, 59Ni, 90Sr, 135Cs and 129I on α-FeOOH, the influences of different pH values, contact time, temperature and ion concentration on the adsorption rate were studied. The adsorption mechanism was also discussed. It was revealed that the adsorption of key nuclides onto α-FeOOH is significantly influenced by both pH and temperature. This change in surface charge corresponds to alterations in the morphology of nuclide ions within the system, subsequently impacting the adsorption efficiency. Sodium ions (Na+) and chlorate ions (ClO3-) compete for coordination with nuclide ions, thereby exerting an additional influence on the adsorption process. The XPS analysis results demonstrate the formation of an internal coordination bond (Ni-O bond) between Ni2+ and iron oxide, which is adsorbed onto α-FeOOH.

Remotely Controlled 3D‐Engineered Scaffolds for Biomimetic In Vitro Investigations on Brain Cell Cocultures

Most in vitro studies regarding new anticancer treatments are performed on 2D cultures, despite this approach imposes several limitations in recapitulating the real tumor behavior and in predicting the effects of therapy on both cancer and healthy tissues. Herein, advanced in vitro models based on scaffolds that support the 3D growth of glioma cells, further allowing the cocultures with healthy brain cells, are presented. These scaffolds, doped with superparamagnetic iron oxide nanoparticles and obtained through 2‐photon polymerization, can be remotely manipulated thanks to an external magnet, thus obtaining biomimetic 3D organization recapitulating the brain cancer microenvironment. From a geometric point of view, the structure is functional to both cell culture on individual unit scaffolds and to tailored cocultures fostered by magnetic‐driven unit assembly, also allowing for cell migration thanks to passages/fenestrations on adjacent structures. Leveraging magnetic dragging, for which a mathematical model is introduced, multiple cocultures are achieved, highlighting the high versatility and the user‐friendly character of the proposed platform that can help overcome the current challenges in 3D cocultures handling, and open the way to the construction of increasingly biomimetic artificial systems.

Design and Characterization of a Dual-Protein Strategy for an Early-Stage Assay of Ovarian Cancer Biomarker Lysophosphatidic Acid.

The overall 5-year survival rate of ovarian cancer (OC) is generally low as the disease is often diagnosed at an advanced stage of progression. To save lives, OC must be identified in its early stages when treatment is most effective. Early-stage OC causes the upregulation of lysophosphatidic acid (LPA), making the molecule a promising biomarker for early-stage detection. An LPA assay can additionally stage the disease since LPA levels increase with OC progression. This work presents two methods that demonstrate the prospective application for detecting LPA: the electromagnetic piezoelectric acoustic sensor (EMPAS) and a chemiluminescence-based iron oxide nanoparticle (IONP) approach. Both methods incorporate the protein complex gelsolin-actin, which enables testing for detection of the biomarker as the binding of LPA to the complex results in the separation of gelsolin from actin. The EMPAS was characterized with contact angle goniometry and atomic force microscopy, while gelsolin-actin-functionalized IONPs were characterized with transmission electron microscopy and Fourier transform infrared spectroscopy. In addition to characterization, LPA detection was demonstrated as a proof-of-concept in Milli-Q water, buffer, or human serum, highlighting various LPA assays that can be developed for the early-stage detection of OC.

Immobilization of Ficin Enzyme onto Surface-Modified Iron Oxide Nanoparticles: Characterization and Catalytic Activity

Immobilization of Ficin Enzyme onto Surface-Modified Iron Oxide Nanoparticles: Characterization and Catalytic Activity

Anti-blue light and hydrophobic composite film based on iron oxide and FAS-modified SiO2

With the increasing application of display and lighting devices, the potential injury to human eyes due to blue light has been attracting significant attention. While current anti-blue light films are complex, costly and low stability in humid environments. In this work, anti-blue light films were fabricated using iron oxide as blue light absorbent and polyvinylpyrrolidone as surfactant, under various Fe3+ concentrations and annealing temperatures. Particularly, the films annealed at 300 °C exhibited 60 % absorption rate of blue light in 400–450 nm wavelength range on average and still maintained 96 % transmittance to 500–800 nm visible light. Moreover, the films coated with 1H,1H,2H,2H-perfluorodecyltriethoxysilane (FAS)-modified SiO2 hydrophobic layer showed high hydrophobicity and sequential humid-heat stability. Meanwhile, no obvious changes occurred in transmittance spectra after keeping at 85 °C and 85 % relative humidity for 15 days. With the composite film covered, the color rendering index of the display screen decreased only 0.7 %, while the blue light weighted radiance decreased significantly by 37.1 %. Furthermore, cell experiments with composite films demonstrated that human retinal pigment epithelium cells were effectively protected from blue light injury. Overall, the composite films with high stability exhibited desired anti-blue light function.

The First Ground-based White Light Lunar Polarization Imaging: A New Kind of FeO Observation on the Near Side of the Moon

Lunar optical polarization is a fascinating phenomenon that occurs when sunlight reflects off the surface of the Moon and becomes polarized. This study employs a novel split-focus plane polarimetric camera to conduct the initial white light polarimetric observations on the near side of the Moon. We obtained the linear degree of polarization (DOP) parameters of white light by observation from the eastern and western hemispheres of the Moon. The findings indicate that the white light polarization is lower in the lunar highland than in the lunar maria overall. Combining the analysis of lunar soil samples, we noticed and determined that the DOP parameters of white light demonstrate high consistency with iron oxide on the Moon. This study may serve as a new diagnostic tool for the Moon.

Investigation of structural, physical and optical properties of sodium boro-tellurite glasses doped with iron oxide

In this work, we demonstrate systematic studies on the influence of Fe2O3 on the structural and optical properties of transparent B2O3–TeO2–Na2O glasses containing the different concentrations of Fe2O3. The glasses were prepared via the standard melt quenching method, and the prepared glasses were characterized using, XRD, electron paramagnetic resonance (EPR), FTIR, and UV–visible spectroscopic techniques. Furthermore, we evaluated several physical properties of the glasses, including densities, molar volume, boron-boron separation, and oxygen packing density, with respect to the concentration of Fe2O3 in the host glass matrix. It is observed that the density of the glasses and the average boron-boron distance found increase with Fe2O3 concentration due to the modification in the glass network induced by the dopant ions. EPR spectra reveals the presence resonance signals at g ∼2.04 and g ∼4.26, hence it proves the existence of Fe3+ in distorted octahedral coordination and supported by UV–Vis absorption bands. The FTIR spectra revealed an increase in spectral intensity with the concentration of Fe2O3. This was attributed to the formation of non-bridging oxygens through converting BO4 units into BO3 units, which Fe2O3 mediated. The UV–visible spectral analysis showed a decreased energy band gap from 2.26 to 1.51 eV with increased Fe2O3 concentration. Additionally, we determined the Urbach energy, refractive index, optical basicity, and electronegativity, which are presented in detail.