Iron Oxide Research Articles

Indium-Iron Oxide Nanosized Solid Solutions as Photocatalysts for the Degradation of Pollutants under Visible Radiation.

A series of solid solutions of indium and iron oxides with different In/Fe ratios (InxFeyO3, with x + y = 2) were synthesized in the form of nanoparticles (diameter of ca. 30-40 nm) with the purpose of generating enhanced photocatalysts with an intermediate band gap compared to those of the monometallic oxides, In2O3 and Fe2O3. The materials were prepared by co-precipitation from an aqueous solution of iron and indium nitrates and extensively characterized with a combination of techniques. XRD analysis proved the formation of the desired InxFeyO3 solid solutions for Fe content in the range 5-25 mol%. UV-Vis absorption analysis showed that the substitution of In with Fe in the crystalline structure led to the anticipated gradual decrease of the band gap values compared to In2O3. The obtained semiconductors were tested as photocatalysts for the degradation of model organic pollutants (phenol and methylene blue) in water. Among the InxFeyO3 solid solutions, In1.7Fe0.3O3 displayed the highest photocatalytic activity in the degradation of the selected probe molecules under UV and visible radiation. Remarkably, In1.7Fe0.3O3 showed a significantly enhanced activity under visible light compared to monometallic indium oxide and iron oxide, and to the benchmark TiO2 P25. This demonstrates that our strategy consisting in engineering the band gap by tuning the composition of InxFeyO3 solid solutions was successful in improving the photocatalytic performance under visible light. Additionally, In1.7Fe0.3O3 fully retained its photocatalytic activity upon reuse in four consecutive cycles.

Advanced Nanomaterials for Cancer Therapy: Gold, Silver, and Iron Oxide Nanoparticles in Oncological Applications.

Cancer remains one of the most challenging health issues globally, demanding innovative therapeutic approaches for effective treatment. Nanoparticles, particularly those composed of gold, silver, and iron oxide, have emerged as promising candidates for changing cancer therapy. This comprehensive review demonstrates the landscape of nanoparticle-based oncological interventions, focusing on the remarkable advancements and therapeutic potentials of gold, silver, and iron oxide nanoparticles. Gold nanoparticles have garnered significant attention for their exceptional biocompatibility, tunable surface chemistry, and distinctive optical properties, rendering them ideal candidates for various cancer diagnostic and therapeutic strategies. Silver nanoparticles, renowned for their antimicrobial properties, exhibit remarkable potential in cancer therapy through multiple mechanisms, including apoptosis induction, angiogenesis inhibition, and drug delivery enhancement. With their magnetic properties and biocompatibility, iron oxide nanoparticles offer unique cancer diagnosis and targeted therapy opportunities. This review critically examines the recent advancements in the synthesis, functionalization, and biomedical applications of these nanoparticles in cancer therapy. Moreover, the challenges are discussed, including toxicity concerns, immunogenicity, and translational barriers, and ongoing efforts to overcome these hurdles are highlighted. Finally, insights into the future directions of nanoparticle-based cancer therapy and regulatory considerations, are provided aiming to accelerate the translation of these promising technologies from bench to bedside.

Application of iron oxide and its composites containing carbon nanoparticles to the solution of environmental problems

The radioactive materials and the secondary waste after a nuclear power plant accident pose a big environmental problem. The nontoxic iron oxide and iron oxyhydroxide, and their composites with carbon materials were applied to solve the problem. Coal oxide produced by modified Brodie method using coal, NaOH, and γ-Fe2O3 were treated by a hydrothermal process. When the diluted dispersion mixture was treated with SrCl2, the composite particles were attracted to a magnet. On the other hand, the composite without SrCl2 was not attracted. This means only the SrCl2-adsorbed composite can be recovered by a magnet. Hematite doped with various amounts of Nb was synthesized. Its catalytic activities for photo-Fenton reaction were investigated for degradation of methylene blue (MB) in the presence of H2O2 under visible light. Nb-doped hematite calcined at 600 ºC produced smaller particles and showed higher catalytic activity than those calcined at 700 ºC. It was shown that the sample with higher Nb doping showed a better catalytic activity, i.e., the sample with 40 atomic percent of Nb calcined at 600 ºC has the highest catalytic activity. The hematite with 7.4 atomic percent of Nb calcined at 600 ºC showed unique characteristics since it has rapid decomposition rate of MB as well as ferrimagnetic-like characteristics, which makes it separable by a magnet. The polymorphism of iron(III) oxyhydroxide was controlled by adding acetic acid, ethylenediamine, and citric acid. The lepidocrocite obtained by adding the additive of citric acid resulted in the presence of citric acid in the particles and revealed a large specific surface area and negative Zeta potential, which showed an extremely high catalytic activity of MB decomposition for photo-Fenton reaction.

SODA LIME SILICATE GLASSES CONTAINING IRON OXIDE - IN VITRO EVALUATION

Three glasses with different iron oxide concentrations (between 5 and 8.1 mol %) were obtained in the CaO - Na2O - SiO2 - Fe2O3 system by using conventional melting-quenching technique. The amorphous nature of the synthesized materials is confirmed by X-ray diffraction analysis, XRD. The physico-chemical and structural characterization of the glasses was performed by measuring their density, refractive indices, as well as by calculating the molar volume, oxygen packing density and recording the infrared spectra by Fourier Transformed Infrared Spectroscopy, FT-IR, respectively. The glasses were evaluated in vitro by examining bone-like apatite formation on their surfaces in a simulated body fluid, SBF. The structural changes in the glasses during the in-vitro test were traced by means of FT-IR and Scanning Electron Microscopy, SEM. The solutions were examined by Inductively Coupled Plasma Optical Emission Spectroscopy, ICP-OES to determine the ion exchange between the glasses and the starting SBF and the corresponding effect on the pH was also recorded.

Enhancement of superconducting properties of grown FeTe0.65Se0.35 single crystals through air annealing

Abstract This work investigates the annealing effects on the superconducting properties of FeTe0.65Se0.35 single crystals. We examine the impact of varying annealing times on the magnetotransport, magnetic, and vortex pinning properties of the single crystals. The structural analysis shows the single crystalline growth of crystals along the c-axis. X-ray photoelectron spectroscopy results confirm the presence of iron oxides in the annealed samples. Temperature-dependent resistivity and magnetization measurements confirm the superconductivity in the as-grown and annealed samples. However, the as-grown sample shows a broad superconducting transition and low superconducting volume fraction, but after annealing, significant improvement in both is observed. Moreover, the self-field critical current density at 2 K is enhanced by a factor of ~4.5 for the optimally annealed sample compared to the as-grown sample. Experimental observations have been analyzed with the theoretical models to understand the effects of annealing on the vortex pinning mechanisms. Further, the specific heat study confirms the bulk superconductivity in the annealed sample compared to the as-grown single crystal. Overall, our study indicates that the superconducting properties vary with the annealing time, and the best results are obtained at an optimum annealing time.

Amino Acid Adsorption Onto Magnetic Nanoparticles Reveals Correlations With Physicochemical Parameters

AbstractWe analyze the adsorption of the proteinogenic amino acids (AAs) glutamine, glutamic acid, lysine, tyrosine, proline, and valine onto bare iron oxide nanoparticles (approx. 10 nm). Aiming to identify the governing principles of low molecular weight coronae, which remain underinvestigated, our study covers broad concentration ranges up to the solubility limit of the AAs. Isothermal experiments reveal that the highly soluble AAs valine, proline, and lysine form extensive multilayers on the nanoparticle surface, and infrared measurements indicate intermolecular interactions, particularly with valine and lysine, for higher AA contents. Conversely, the low solubility of tyrosine and glutamic acid restricts their adsorption capacity, despite their higher partitioning on the solid surface. Parameters derived from fitting a classic saturation model seem to align with well‐documented physicochemical properties such as the hydrophobicity and the complexity indices – a promising first step towards formulating design principles. Scaling these parameters by the AA solubility reveals a clear correlation with the adsorption behavior. In adsorption experiments with AA model mixtures, sequential incubation increases the adsorption capacity for valine and proline, whereas simultaneous incubation with these AAs reduces tyrosine's capacity. Future studies should seek to elucidate adsorption patterns to advance our understanding of corona growth and evolution mechanisms.

Magnetic Effects in Textile Fibers Filled with Nanoconstituents Based on Iron Oxides

ABSTRACT The paper proves the possibility of providing magnetic properties in the process of saturation of textile fibers with a nanomixture of divalent and trivalent iron oxides. The mechanisms of interaction of nanostructures with natural and synthetic fibers are analyzed. The peculiarities of the introduction of magnetic components into flax, cotton, polyamide, and polyester fibers are determined. The relative number of particles with nanoscale in the total was statistically proved. To evaluate the macro effects of saturation, the relative amount of the accumulated mixture of divalent and trivalent iron oxides was determined, taking into account the previous fiber weight. Two basic constants characterizing the properties of textile fibers to magnetic interaction are proposed. It is proved that flax fibers exhibit the highest magnetic efficiency. The average size of iron oxide nanoparticles is 80–90 nanometers, which is confirmed by studies using electron microscopy. The final magnetization of the obtained textile materials provides an attractive magnetization of 20–30 mPascal. The magnetic field of magnetic textile fibers acts at a height of up to 6–7 mm. The directions of the use of fibers with magnetic properties are shown as a prospect for the development of textile smart products.

Kinetic Analysis of Molten Oxide Reduction Using Bottom-Blown Hydrogen Injection

Hydrogen-based smelting reduction has received widespread attention as an important technology for realizing low-carbon development in hydrogen metallurgy. In this study, the thermodynamics of smelting reduction was firstly analyzed by using FactSage 8.1 thermodynamic software, on the basis of which smelting reduction experiments of iron oxides by using bottom-blown hydrogen were carried out. The experiments used oxidized pellets as experimental materials, and the effects of the reduction process were analyzed in terms of the reduction temperature, the reduction time, and the hydrogen flow rate. The experimental results show that under the experimental conditions of a temperature of 1550 °C and a hydrogen flow rate of 0.2 Nm3/h, the reduction rate of iron oxides in the process of reducing iron oxides by hydrogen is significantly faster in the first 10 min than after 10 min. The hydrogen utilization rate reached a maximum of 41.87%, then decreased continuously and finally maintained at about 20%. Using the method of model fitting, it was found that the hydrogen-based molten reduction conformed to the phase boundary reaction model (Gα=1−(1−α)1/2), the corresponding mechanism function is fα=2(1−α)1/2, where α stands for the reduction conversion, and the reaction rate constant k(T) is 2.37 × 10−4 s−1 under the experimental conditions.

Ambient Sunlight Driven Photothermal Green Syngas Production at 100 m3 Scale by the Dynamic Structural Reconstruction of Iron Oxides with 38.7% Efficiency

AbstractAmbient sunlight‐driven photothermal green syngas production via reverse water‐gas shift (RWGS) reaction is important for carbon neutrality, which lacks efficient and inexpensive catalysts at low temperatures. This studydemonstrates that the scalable Fe3O4 supported with K atoms modified Ag nanoparticles (AgK/Fe3O4) exhibits a RWGS CO production rate of 1089 mmol g−1 h−1 at 300 °C and 100% CO selectivity through dynamic structural reconstruction, surpassing all reported platinum‐based catalysts. In situ characterization and theoretical simulation indicate that the AgK nanoparticles activate H2 to reduce Fe3O4 as metallic Fe. Subsequently, the metallic Fe spontaneously reacts with CO2 to form CO and Fe3O4, thereby facilitating low‐temperature RWGS. Owing to its superior low‐temperature performance, AgK/Fe3O4 equipped with a homemade photothermal device achieves one sun‐driven photothermal RWGS with a CO production rate of 1925 mmol g−1 h−1 and a 38.7% solar to enthalpy energy conversion efficiency. Furthermore, the enlarged outdoor demonstration yields 100.6 m3day−1 of green syngas with an H2/CO ratio of 3. This work paves the way for designing efficient platinum‐free CO2 hydrogenation catalysts and introduces a new approach for sunlight‐driven scalable green syngas production.

Analysis of Oxide Layer Formation During Oxidation of AISI 4140 Steel at 1000 °C over Exposure Time

The high-temperature shaping of steels is accompanied by the formation of surface scales composed of oxide layers. However, the oxidation kinetics and morphology of these scales remain poorly understood. This study analyses the formation of oxide layers on AISI 4140 steel at varying oxidation times (20, 40 and 60 min) at 1000 °C. The analysis revealed the presence of hematite, magnetite, and transformed wustite in the oxide layers, along with clusters of alloying element oxides, predominantly chromium and iron oxide (FeCr2O4). There was a direct correlation between the duration of the oxidation process and the thickness of the scale and the number of defects observed in the material. The coating layer of alloying element oxides demonstrated insufficient adhesion to the steel substrate. Similarly, the oxides of alloying elements within this layer exhibited low cohesion among themselves. The alloying elements are present in all oxide layers, but in greater quantity in the layer in contact with the steel substrate, where a reduction in their concentrations was observed over time. This indicates that the alloying elements tend to disperse as the thickness of the alloying element oxide layer increases over time.

Looking at the Modern to Better Understand the Ancient: Is It Possible to Differentiate Mars Pigments from Archaeological Ochres?

This article offers a discussion of the possibility of distinguishing ochres from Mars pigments. The discussion addresses technological, archaeological, and artistic aspects. Natural earth pigments such as ochres, siennas, and umbers have been widely used from the Paleolithic to the present day and still find wide application despite the development of synthetic iron oxide pigment synthesis processes, called Mars pigments. The potential ability of today’s analytical techniques to distinguish between two classes of pigments of the same color with very similar chemical composition—but perhaps sufficient for reliable recognition—is also discussed. The paper begins by addressing the proper use of the terms “ochres” and “Mars pigments” and their accurate identification in artworks. It reviews the literature on the chemical–mineralogical characterization of yellow and red iron pigments and analyzes pigment catalogs to understand how companies distinguish ochres from Mars pigments. An experimental analysis using External Reflection Infrared Spectroscopy (FTIR-ER) compared painting samples made with natural ochres and Mars pigments, confirming the literature findings and suggesting future research directions. Key differences such as hematite in yellow ochres and specific spectral peaks in red ochres support the potential of FTIR-ER spectroscopy as a noninvasive tool for distinguishing pigments, especially for fragile artifacts and archaeological applications.

Synthesis of Oil-Soluble Polymer-Grafted Carbon Dots with Outstanding Colloidal Stability and Tribological Properties in Polyalphaolefin.

Herein, a series of polylauryl methacrylate-grafted CDs (CDs-PLMA-m, m denotes the reaction time in hours) with core-shell structure were synthesized via surface-initiated atom-transfer radical polymerization (SI-ATRP). Due to the good solubility of PLMA in hydrocarbons, all of the CDs-PLMA-m can be facilely dispersed in polyalphaolefin (PAO) to form pellucid colloidal dispersions. The reciprocating ball-on-plate sliding friction tests proved that the addition of 3.0 wt % CDs-PLMA-1 markedly lessened the wear and friction of PAO by 53.0 and 40.0%, respectively. The tribological performances of the CDs-PLMA-1 (3.0 wt %)/PAO dispersion did not attenuate sharply when the friction duration extended from 20 to 200 min or the applied load increased from 20 to 100 N, revealing the long lifetime and desirable load-carrying effect of CDs-PLMA-1. Based on the friction tests, the antifriction behavior of CDs-PLMA-1 was related to the synergies between the molecular lubrication of PLMA-1 brushes and the nanolubrication of CDs. Furthermore, the wear analyses disclosed the deposition of tribofilm composed of a lot of CDs-PLMA-1 and a spot of iron oxides, which provided oxidation resistance and an antiwear function. This study established a reliable route to the synthesis of oil-soluble polymer-grafted CDs, enabling high-efficiency lubrication of CDs in PAO.

Defect Engineering with Rational Dopants Modulation for High-Temperature Energy Harvesting in Lead-Free Piezoceramics

HighlightsThe solution limit of manganese ion in BiFeO3–BaTiO3 (BF–BT) was determined by combining multiple advanced characterization methods.The defect engineering associated with fine doping can realize the co-modulation of polarization configuration, iron oxidation state and domain orientation.The BF–BT–0.2Mn piezoelectric energy harvester shows excellent power generation capacity at 250 °C, which is an important breakthrough for lead-free piezoelectric devices.

Exploring Multi-Parameter Effects on Iron Oxide Nanoparticle Synthesis by SAXS Analysis

Iron oxide nanoparticles (IONs) are extensively used in biomedical applications due to their unique magnetic properties. This study optimized ION synthesis via the co-precipitation method, exploring the impact of the reactant concentrations (Fe(II) and Fe(III)), NaOH concentration, temperature (30 °C–80 °C), stirring speed (0–1000 rpm), and dosing rate (10–600 s) on particle size and growth. Using small-angle X-ray scattering (SAXS), we observed, for example, that higher temperatures (e.g., 67 °C compared with 53 °C) led to a 50% increase in particle size, while the stirring speed and NaOH concentration also influenced nucleation and aggregation. These results provide comprehensive insights into optimizing synthetic conditions for targeted applications in biomedical fields, such as drug delivery and magnetic resonance imaging (MRI), where precise control over nanoparticle size and properties is crucial.

Efficient separation of cerium from rare earth elements and major impurities using low cost manganese ferrites from highly acidic solutions

Sorption of REEs using spinel-ferrite nanoparticles has received great attention in the last decades, because of combining the advantages of iron and manganese metal oxides. Nano-manganese ferrite (MnFe2O4) was successfully synthesized using the co-precipitation method and modified with the addition of zinc to produce (Mn0.8Zn0.2Fe2O4). The synthesized materials were characterized using FTIR, SEM with EDX-mapping, XRD, chemical stability, and surface area. Several process parameters were studied to optimize the efficiency of Ce(III) separation from La(III), Eu(III), Pb(II), and Fe(III) from highly acidic media. The parameters include contact time, solution pH, and metal ion concentration. The sorption process was well fitted to the pseudo-2nd order model, which confirms the chemical nature of the sorption process where equilibrium was achieved after 30 minutes. The pH study's findings demonstrate that Ce(III) was most effectively separated at a very high, acidic pH of 0.5. Both MnFe2O4 and Mn0.8Zn0.2Fe2O4 have high chemical stability in different media where the weight loss was less than 10 %. The correlation coefficient and residual errors analysis confirm that the non-linear extended sips isotherm model more accurately expresses the behavior of the sorption process than the non-linear Freundlich and Langmuir isotherm models. The modified material Mn0.8 Zn0.2Fe2O4 shows higher sorption capacities for all the studied metal ions than MnFe2O4. The maximum sorption capacities of Ce(III), La(III), Eu(III), Pb(II), and Fe(III) in the mixture were 59.2, 6.5, 6.3, 15.4, and 13.7 mg/g, respectively.

Augmenting Protein Degradation Capacity of PROTAC through Energy Metabolism Regulation and Targeted Drug Delivery.

The ubiquitin-proteasome system (UPS) is responsible for degrading over 70-80% of cellular proteins. Consequently, proteolysis-targeting chimeras (PROTACs) are developed to induce the ubiquitination and subsequent degradation of proteins of interest (POIs) by the UPS. To amplify the therapeutic efficacy of PROTACs, energy metabolism regulation is first harnessed to boost UPS function in tumor cells. Proteomic and ubiquitinome analyzes reveal that total ubiquitinated proteins and proteasome activity are significantly increased in 143B and MDA-MB-231 tumor cells following fasting-mimicking diet (FMD) treatment. As a result, the degradation efficiency of PROTACs targeting focal adhesion kinase (FAK-P) or bromodomain-containing protein 4 (BRD4-P) is significantly enhanced in FMD-treated 143B and MDA-MB-231 tumor cells. Then, silica-coated iron oxide nanoparticles are developed modified with tumor cell membranes for targeted delivery of PROTACs. Magnetic resonance imaging (MRI) and fluorescence imaging confirm that nanocarriers significantly improve the delivery efficiency of PROTACs in FMD-treated 143B or MDA-MB-231 tumors. In vivo studies demonstrate that the antitumor efficacy of FAK-P and BRD4-P is greatly augmented when combined with targeted delivery and FMD treatment. Overall, this study presents a strategy to enhance the efficacy of PROTACs in cancer therapy.

Tailoring of magnetite nanocomposite of carboxymethyl chitosan (CMCs) impregnated with iron (III) oxide for enhanced degradation of reactive blue 19 dye and inactivation of harmful microbes in wastewater

The study investigates the fabrication of an innovative nanocomposite composed of carboxymethyl chitosan (CMC) combined with different amounts of iron (III) oxide (Fe₂O₃) to boost dye degradation and antibacterial effectiveness. A top-down ball milling technique formed the nanocomposites and was extensively investigated for their structural, morphological, and functional features. The mean particle size of the 0.3Fe₂O₃/CMC and 0.6Fe₂O₃/CMC nanocomposites was measured at 83.74 nm and 124.5 nm, respectively, with polydispersity index (PdI) values suggesting satisfactory homogeneity. The adsorption effectiveness of Reactive Blue 19 (RB 19) dye was evaluated under different circumstances, with the 0.6Fe₂O₃/CMC nanocomposite exhibiting the maximum adsorption capacity of 140 mg/g at an ideal pH of 5. Kinetic analyses indicated that the adsorption process adhered to a pseudo-second-order kinetic model. The nanocomposites had significant bactericidal performance, with the 0.6Fe₂O₃/CMC nanocomposite exhibiting the most extensive inhibition zones, particularly against E. coli (28.4 mm) and Pseudomonas aeruginosa (23.2 mm). Furthermore, the reusability of the 0.6Fe₂O₃/CMC nanocomposite was validated by five adsorption-desorption cycles, retaining over 90 % efficiency. The results underscore the efficacy of Fe₂O₃/CMC nanocomposites as viable materials for wastewater treatment and antibacterial purposes, offering a promising approach for environmental remediation.

High-performance α-Fe2O3 nano cubes as anode for supercapacitors

Abundant availability, high theoretical specific capacitance and low cost of transition metal oxides such as iron oxides, make them attractive as electrode materials for energy storage. In order to achieve improved performance, high conductivity, shorter ion-diffusion path, and faster ion accessibility, rational design of morphology of electrode material is highly desirable. We have successfully synthesized mesoporous α-Fe2O3 nanocubes to achieve high specific capacitance and better retention. The as-prepared and annealed α-Fe2O3 nanocubes show high reversible redox activity along with good thermodynamic stability. These nanostructure give rise to high specific capacitance and ~90 % of the capacitance can be retained even after 1000 redox cycles, suggesting good cyclic stability. The electrochemical performance of mesoporous α-Fe2O3 nanocubes is attributed to the morphological features, which results in efficient K+ ion transport into the pores. A two electrode α-Fe2O3//NiO device is fabricated, which shows excellent power and energy density of ∼627 W/kg and ∼23.32 Wh/kg, respectively. Our work demonstrates that 3D nanoporous α-Fe2O3 electrodes forms promising material system as anode for improved charge storage performance.

Vertical Variability in morphology, chemistry and optical properties of the transported Saharan air layer measured from Cape Verde and the Caribbean.

The structural properties of the Saharan air layer (SAL) including chemical, morphological and optical properties were measured during the Saharan Aerosol Longrange TRansport and Aerosol Cloud interaction Experiment (SALTRACE- June/July 2013). Flight measurements were done from Cape Verde and the Caribbean. Changes happening with the chemical composition, mixing, shape and absorption of aerosol single particles (particle diameter range 0.5-3.0 µm) inside SAL during its transport are detailed. Dust-dominated SAL (relative number abundance >90%) and generally low mixing (<1% with sea-salt and sulphates) are observed at both locations. The change in shape (determined as aspect ratio (AR)) after transatlantic transport was statistically not significant. The iron oxide fraction, important for light absorption, contributed 6.0-6.8% to SAL dust. A lower amount of Fe oxides was observed in transported SAL, especially for the size range 0.5-1.5 µm. This reduction in Fe oxide content resulted in a 4% decrease (0.0046-0.0044) in dust imaginary refractive index and a 1% decrease in single scattering albedo (0.802-0.809) at 520 nm. Our work suggests including the size distribution of iron oxides and their particular behaviour in future experiment/model studies.

Preliminary investigation on spent garnet as a novel supplementary cementitious material

The escalating global demand for cement, a fundamental material in infrastructure development, has exacerbated environmental challenges, particularly through significant carbon dioxide (CO₂) emissions, which account for approximately 8.3 % of global anthropogenic CO₂ output. This research explores the potential of spent garnet powder, a byproduct of abrasive water jet machining, as a sustainable supplementary cementitious material (SCM) to mitigate these impacts. The spent garnet powder, characterized by a high concentration of silicon dioxide (SiO₂), aluminum oxide (Al₂O₃), and iron oxide (Fe₂O₃), was subjected to rigorous analysis. X-ray Fluorescence (XRF) confirmed its chemical suitability for pozzolanic applications, while laser particle size analysis revealed a finer granulometry relative to Ordinary Portland Cement (OPC), which is advantageous for enhancing pozzolanic reactivity. Scanning Electron Microscopy (SEM) demonstrated the angular and irregular morphology of the garnet particles, which is conducive to improved interfacial bonding within the cement matrix. X-ray Diffraction (XRD) identified active mineral phases that are critical for promoting pozzolanic reactions, and Thermogravimetric Analysis (TGA) demonstrated the material’s superior thermal stability, with minimal decomposition at elevated temperatures. Fourier Transform Infrared Spectroscopy (FTIR) identified strong silicon-oxygen (Si-O) and aluminum-oxygen (Al-O) bond structures, indicative of robust pozzolanic potential. The Strength Activity Index (SAI) and Frattini tests further substantiated the pozzolanic activity, revealing that a 10 % replacement of OPC with SGP not only enhances compressive strength but also meets the stringent requirements of ASTM C618. Additionally, the economic analysis underscores the cost-effectiveness of utilizing spent garnet powder, presenting a viable strategy for reducing both production costs and CO₂ emissions in the cement industry. This study conclusively positions spent garnet powder as a highly promising supplementary cementitious material, with significant implications for advancing sustainable construction practices and reducing the environmental footprint of cement production.