Silica Oxide Research Articles

Invitro Activity of Mineral Trioxide Aggregate Modification from Rice Hull Ash Silica and Calcium Oxide from Clamshells

The impact of SrO particles and hydroxyapatite (HA) on the characteristics of Mineral Trioxide Aggregate (MTA) from silica Rice Husk Ash (RHA) and Precipitated Calcium Carbonate (PCC) from clam shell has been studied in this research. Silica and calcium oxide are used as material to form tricalcium silicate (C3S) and dicalcium silicate (C2S) in MTA. Bi2O3 and SrO were added in MTA with 18% (w/w) total percentage. MTA was made with a sol-gel process and used catalyst NH3. After synthesis, material was calcined at 1000 oC for 3 h. HA was added at percentages of 3, 6, and 9% in 5% SrO modified MTA to see the effect of its addition on the material. The modified MTA (MTA-SrO-HA) were hydrated water using water to powder method with ratio of 3:1. The MTA-SrO5/HA6 showed higher compressive strength and dentine interaction to the commercial MTA (Proroot brand) in days 3 and 7. This material had potential as a root canal filling in dental endodontic treatment.

Facilitating macroscopic superlubricity through graphene oxide nanosheet additives in phosphoric acid

The field of superlubricity is garnering significant global interest amid the ongoing energy crisis. Various liquids can achieve superlubricity under ambient conditions; however, this limits their applications, such as in acidic environments. Consequently, enhancing anti-wear properties and reducing the coefficient of friction (COF) have become pressing challenges. Graphene-based materials are being extensively studied for tribological applications, attributed to their unique molecular structures and lubricating properties, often serving as lubricating additives to significantly reduce COF. In this study, graphene oxide (GO) nanosheets were utilized as lubricating additives in phosphoric acid (H3PO4; pH = 1.5) to explore lubrication enhancement in acidic environments. An ultralow COF of 0.001 was achieved, accompanied by reduced surface roughness and increased contact pressure (by 96.42 %), following the lubrication with GO-H3PO4. The reduction in COF post-lubrication with GO-H3PO4 is ascribed to three primary factors: the formation of a tribofilm via chemical reactions (comprising silica and phosphorus oxide layers), the hydrogen bond effect leading to a hydrated water layer with low shear strength, and the adsorption of GO nanosheets on the friction surface, facilitating friction transfer from Si3N4/Si3N4 to GO/GO.

Biogenic-to-lithogenic handoff of particulate Zn affects the Zn cycle in the Southern Ocean.

Zinc (Zn) is vital to marine organisms. Its active uptake by phytoplankton results in a substantial depletion of dissolved Zn, and Zn bound to particulate organic matter replenishes dissolved Zn in the ocean through remineralization. However, we found that particulate Zn changes from Zn bound to phosphoryls in cells to recalcitrant inorganic pools that include biogenic silica, clays, and iron, manganese, and aluminum oxides in the Southern Ocean water column. The abundances of inorganic pools increase with depth and are the only phases preserved in sediments. Changes in the particulate-Zn speciation influence Zn bioavailability and explain the decoupling of Zn and phosphorus and the correlation of Zn and silicon in the water column. These findings reveal a new dimension to the ocean Zn cycle, implicating an underappreciated role of inorganic Zn particles and their impact on biological productivity.

Synthesis and Optical Properties of a Novel Hybrid Nanosystem Based on Covalently Modified nSiO2 Nanoparticles with a Curcuminoid Molecule.

A new curcuminoid molecule (3) has been designed and synthesized, containing a central -(CH2)2-COOH chain at the α carbon of the keto-enol moiety in the structure. The carboxylic acid group is added to react with exposed amino groups on silica oxide nanoparticles (nSiO2), forming an amide bond to attach the curcuminoid moiety to the nSiO2 covalently. The Kaiser test quantifies the functionalization degree, yielding 222 μmol of curcuminoid per gram of nanoparticles. The synthesized hybrid nanosystem, nSiO2-NHCO-CCM, displays significant emission properties, with a maximum emission at 538 nm in dichloromethane, similar to curcuminoid 1 (without the central chain), which emits at 565 nm in the same solvent. Solvent-induced spectral effects on the absorption and emission bands of the new hybrid nanosystem are confirmed, similar to those observed for the free curcuminoid (1). The new nanosystem is evaluated in the presence of kerosene in water, showing an emission band at 525 nm as a detection response. The ability of nSiO2-NHCO-CCM to change its fluorescence when interacting with kerosene in water is notable, as it overcomes the limitation caused by the insolubility of free curcuminoid 1 in water, allowing for the exploitation of its properties when connected to the water-stable nanosystem for future detection studies.

LHHW/RSM reaction rate modeling for Co-Mn/SiO2 nanocatalyst in Fishcher-Tropsch synthesis

This study aims to assess the kinetics of Fischer–Tropsch (FT) reaction over the cobalt-manganese nanoparticles supported by silica oxide. Nanoparticles were synthesized by the thermal decomposition method using "[Co(NH3)4CO3]MnO4" complex and characterized by XRD, TEM, and BET techniques. The kinetics of the process were evaluated using a combination of Langmuir–Hinshelwood-Hougen-Watson (LHHW) and response surface methodology. Correlation factors of 0.9902 and 0.962 were obtained for the response surface method (RSM) and LHHW, respectively. The two methods were in good agreement, and the results showed that the rate-determining step was the reaction of the adsorbed methylene with the adsorbed hydrogen atom, and only carbon monoxide molecules were the most active species on the catalyst surface. A temperature of 502.53 K and a CO partial pressure of 2.76 bar are proposed as the optimal conditions by RSM analysis. The activation energy of CO consumption reaction was estimated to be 61.06 kJ/mol.

Effect of Curing Time and Variations in Na2SiO3: NaOH Ratio on the Mechanical Properties of Fly Ash-based Geopolymer Artificial Aggregates using the Crushing Method

Burning coal to produce electrical energy in PLTU produces waste in the form of fly ash. This waste must be managed properly so that it does not cause detrimental environmental effects. Fly ash has potential as a building material because it contains silica, aluminum, and other oxides that can react with alkaline solutions to form geopolymer compounds. Geopolymer has good mechanical properties and is resistant to acidic and alkaline environments. The development of the crushing method for aggregate materials, artificial geopolymers, and fly ash is an interesting work direction because it can utilize fly ash waste and reduce the dependence on aggregates. Moreover, this material can be used to help reduce the effects of development construction on the environment. The crushing method is utilized to obtain geopolymer artificial aggregate with the desired size. Aggregates can be destroyed to become small particles by using destruction techniques and mechanical crushing tools, such as hammer mills, jaw crushers, and ball mills. The aggregate impact value (AIV) percentage reaches 13.20% at a Na2SiO3/NaOH ratio of 2, but it decreases to 12.64% at a Na2SiO3/NaOH ratio of 3.5. The AIV percentage reaches 12.82% without the addition of sand, but it decreases to 12.64% when the added amount of sand is 20%. The AIV percentage increases to 12.76% when the added sand is 40%. Moreover, the AIV percentage reaches 12.64% after curing for 24 hours, decreases to 12.46% after 48 hours of curing, and increases to 12.94% after 72 hours of curing.

Assessment of the Effect of Surface Modification of Metal Oxides on Silver Nanoparticles: Optical Properties and Potential Toxicity.

Silver nanoparticles (AgNPs) have garnered significant interest due to their distinctive properties and potential applications. Traditional fabrication methods for nanoparticles often involve high-energy physical conditions and the use of toxic solvents. Various green synthesis approaches have been developed to circumvent these issues and produce environmentally benign nanoparticles. Our study focuses on the green synthesis of AgNPs using L-ascorbic acid and explores the modification of their properties to enhance antibacterial and anticancer effects. This is achieved by coating the nanoparticles with Zinc oxide (ZnO) and Silica oxide (SiO2), which alters their optical properties in the visible spectrum. The synthesized formulations-AgNPs, zinc oxide-silver nanoparticles (Ag@ZnO), and silica oxide-silver nanoparticles (Ag@SiO2) core/shell nanoparticles-were characterized using a suite of physicochemical techniques, including Transmission Electron Microscopy (TEM), Dynamic Light Scattering (DLS), Zeta potential measurement, UV-Vis spectroscopy, Refractive Index Measurements, and Optical Anisotropy Assessment. TEM imaging revealed particle sizes of 11 nm for AgNPs, 8 nm for Ag@ZnO, and 400 nm for Ag@SiO2. The Zeta potential values for Ag@ZnO and Ag@SiO2 were measured at -17.0 ± 5 mV and -65.0 ± 8 mV, respectively. UV-Vis absorption spectra were recorded for all formulations in the 320 nm to 600 nm wavelength range. The refractive index of AgNPs at 404.7 nm was 1.34572, with slight shifts observed for Ag@ZnO and Ag@SiO2 to 1.34326 and 1.37378, respectively. The cytotoxicity of the nanocomposites against breast cancer cell lines (MCF-7) was assessed using the MTT assay. The results indicated that AgNPs and Ag@ZnO exhibited potent therapeutic effects, with IC50 values of 494.00 µg/mL and 430.00 µg/mL, respectively, compared to 4247.20 µg/mL for Ag@SiO2. Additionally, the antibacterial efficacy of AgNPs was significantly enhanced under visible light irradiation. Ag@ZnO demonstrated substantial antibacterial activity both with and without light exposure, while the Ag@SiO2 nanocomposites significantly reduced the inherent antibacterial activity of silver. Conversely, the Ag@ZnO nanocomposites displayed pronounced antibacterial and anticancer activities. The findings suggest that silver-based nanocomposites, particularly Ag@ZnO, could be practical tools in water treatment and the pharmaceutical industry due to their enhanced therapeutic properties.

Role of particle material and geometry in the ballistic performance of nanoparticle-impregnated Kevlar fabric

The possibility of enhancing the ballistic performance of aramid fabrics such as Kevlar through the impregnation of nanoparticles is well established. In this study, the influence of the nanoparticle’s specifications such as size, shape, and material on the underlying mechanisms is investigated. A colloid-based treatment process is used to impregnate dry nanoparticles into Kevlar fabric. Using a customized gas gun rig, neat and treated samples are tested to determine the kinetic energy absorbed. Silica, alumina, and zinc oxide nanoparticles ranging from 10 to 125 nm, with spherical or cylindrical shape are considered. Silica treated samples perform significantly better (83% increase in energy absorbed vs neat fabric) than alumina or zinc oxide treated samples, likely due to greater agglomeration between yarn interfaces leading to enhanced frictional mechanisms. The exit-face damaged zone area acts as a surrogate for energy absorbed as it correlates well across all samples. Compared to samples with three layers treated individually, samples with three layers treated together display a 21% enhancement in the energy absorbed. Specific energy absorbed for three layers treated together with 80-nm silica is nearly 3 times higher than that for the neat fabric. Samples with three layers treated together with 80-nm silica provide the same performance as the neat fabric for a projectile that is nearly 70 m/s faster. Hybrid structural materials such as nanoparticle-fabric composites offer a promising route to enhance ballistic performance without weight penalty, while being amenable to multifunctional applications.

Silica extraction from sodium silicate for wollastonite synthesis at low temperatures

In this study, ceramic wollastonite was prepared at low temperatures by using amorphous silica and calcium oxide powders. The amorphous silica was extracted from sodium silicate, while calcium oxide (CaO) was obtained through the calcination of calcium carbonate (CaCO3) particles. The effect of reaction temperature on the formation of wollastonite was systematically investigated. The synthesized powders were analyzed using various characterization techniques, including X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The results indicate that the synthesized silica nanopowders exhibit a notable surface area, with specific surface area (SSA) values reaching 148 m²/g for samples subjected to calcination at 600°C. Furthermore, based on XRD and differential scanning calorimetry (DSC) analyses, it is evident that β-CaSiO3 forms at approximately 780°C and subsequently undergoes complete transformation into α-CaSiO3 at 1200°C. Notably, this study underscores that the utilization of amorphous silica expedites wollastonite formation at lower temperatures compared to those reported in existing literature.

Influence of Silica Oxide Nanofluid for Different Concentrations on Photovoltaic Cell

Photovoltaic (PV) cells, a renewable fuel, are widely employed. A conventional PV cell also loses efficiency as the temperature rises. This research addresses this issue by cooling the PV cell with nanofluid, specifically SiO2 and distilled water. Applying SiO2 nanofluid experimentally using a real experimental setup is hoped to cool the PV cell’s surface as it becomes heated. This research aims to use distilled water and various concentrations of SiO2 nanofluid, such as 0.1 wt%, 0.2 wt%, and 0.3 wt% on Photovoltaic Cell and flow rate of 2 LPM and a radiation rate of 800 W/m2. ANSYS is used to confirm experimental results by using SiO2 as a nanofluid to lower the PV cell’s temperature and boost its thermal efficiency. The experiment’s findings demonstrated that utilizing nanofluid as a coolant boosted the PV cell’s thermal efficiency and decreased its temperature. Results showed that the thermal efficiency increased with the use of nanofluid as a coolant and with increasing mass concentration. Thermal efficiency values for distilled water, 0.1%, 0.2%, and 0.3% SiO2 were 35.56%, 79.91%, 91.04%, and 104.01%, respectively. This study also discovered that SiO2 works better in terms of cooling the PV cell than normal fluid because of its higher thermal conductivity. The experimental and numerical data show the same decline in PV cell surface temperature and thermal efficiency, unlike the computational results.

Heat and mass transfer analysis of Casson-based hybrid nanofluid flow in the presence of an aligned magnetic field: An application toward mechanical engineering

This examination explores the flow of a hybridized nanofluid (HyNf) containing silica and tin oxide nanoparticles mixed with engine oil (EO/SnO2-SiO2). The flowing occurs via a permeable material constrained by a semi-infinite flat plate. The study takes into account various factors such as convective heat and mass transference, chemical reactions, the Dufour effect, the Lorentz force, thermal radiative fluxing, and radiative absorbing. The research involves converting the managing formulas of the flowing model into a dimensionless form and applying the regular perturbation procedure to find solutions for the rate of fluid flow, temperature, and species diffusion. The surface frictional factor, Nusselt quantity, and Sherwood quantity reflect the shearing stress, rates of heat transference, and rates of mass transport at the plate, respectively. An analysis is conducted on the impact of several factors, including the suction variable, magnetic variable, radiation-absorbing factor, Casson parameter, and Dufour number, on the flow and related quantities. This analysis is based on an examination of graphs and tables. The findings suggest that the heat transference rate in the Casson hybridized nanofluid is better than that in the mono nanofluid. It is exposed that the temperature reduces at the plate having improved frequency of oscillation and also fluid velocity declines for improving values of aligned magnetized field [Formula: see text], but it shows the reverse phenomenon with Gr1 and Gc1.

Inorganic nanocarriers based on calcium carbonate and silica oxide for passive breast cancer targeting

Inorganic nanocarriers based on calcium carbonate and silica oxide for passive breast cancer targeting

Optimizing Synergistic Silica–Zinc Oxide Coating for Enhanced Flammability Resistance in Cotton Protective Clothing

This study reports process optimization studies of silica and zinc oxide-based flame-retardant (FR) coatings on cotton fabric for protective clothing and enhanced flammability properties. The experiments were designed by central composite design (CCD) using response surface methodology (RSM) to assess the synergistic protective effects of silica and zinc oxide FR coating. These prepared sols were coated on cotton fabrics by a simple dip dry cure process. The resulting FR-finished fabrics were characterized by SEM, mechanical properties, flame retardancy, and air permeability. SEM results confirmed the homogenous spreading of particles on cotton fabrics. From TGA results, it was noticed that the incorporation of silica and ZnO in the prepared nano-sols results in improved thermal stability of the FR-finished fabrics. These sol–gel-treated FR cotton fabrics showed excellent comfort properties, which shows their suitability for fire-retardant protective clothing. RSM analysis proved that the predicted values are in good agreement with the experimental values since R2 values for time to ignite, flame spread time, and air permeability were greater than 0.90. The optimized concentration of silica and ZnO in FR-finished fabrics was found to be 0.302% and 0.353%, respectively, which was further confirmed by confirmatory experiments. The optimization analysis successfully optimized the process for synergistic coating of silica and zinc oxide nanoparticles for enhanced flammability properties of FR cotton fabric for protective clothing.

Unveiling the Influential Factors and Heavy Industrial Applications of Graphene Hybrid Polymer Composites

Graphene hybrid-filler polymer composites have emerged as prominent materials that revolutionize heavy industries. This review paper encapsulates an in-depth analysis of different influential factors, such as filler/graphene type, aspect ratios, dispersion methods, filler-matrix compatibility, fiber orientation, synergistic effects, different processing techniques, and post-curing conditions, which affect the processing and properties of graphene hybrid polymer composites, as well as their resultant applications. Additionally, it discusses the substantial role of graphene reinforcement with other fillers, such as carbon nanotubes, silica, nano-clays, and metal oxides, to produce functionalized hybrid polymer composites with synergistically enhanced tailored properties, offering solutions for heavy industries, including aerospace, automotive, electronics, and energy harvesting. This review concludes with some suggestions and an outlook on the future of these composite materials by emphasizing the need for continued research to fully optimize their potential.

Cascade Nanoreactor Employs Mitochondrial-Directed Chemodynamic and δ-ALA-Mediated Photodynamic Synergy for Deep-Seated Oral Cancer Therapy.

The management of oral squamous cell carcinoma (OSCC) poses significant challenges, leading to organ impairment and ineffective treatment of deep-seated tumors, adversely affecting patient prognosis. A cascade nanoreactor that integrates photodynamic therapy (PDT) and chemodynamic therapy (CDT) for comprehensive multimodal OSCC treatment is introduced. Utilizing iron oxide and mesoporous silica, the FMMSH drug delivery system, encapsulating the photosensitizer prodrug δ-aminolevulinic acid (δ-ALA), is developed. Triphenylphosphine (TPP) modification facilitates mitochondrial targeting, while tumor cell membrane (TCM) coating provides homotypic targeting. The dual-targeting δ-ALA@FMMSH-TPP-TCM demonstrate efficacy in eradicating both superficial and deep tumors through synergistic PDT/CDT. Esterase overexpression in OSCC cells triggers δ-ALA release, and excessive hydrogen peroxide in tumor mitochondria undergoes Fenton chemistry for CDT. The synergistic interaction of PDT and CDT increases cytotoxic ROS levels, intensifying oxidative stress and enhancing apoptotic mechanisms, ultimately leading to tumor cell death. PDT/CDT-induced apoptosis generates δ-ALA-containing apoptotic bodies, enhancing antitumor efficacy in deep tumor cells. The anatomical accessibility of oral cancer emphasizes the potential of intratumoral injection for precise and localized treatment delivery, ensuring focused therapeutic agent delivery to maximize efficacy while minimizing side effects. Thus, δ-ALA@FMMSH-TPP-TCM, tailored for intratumoral injection, emerges as a transformative modality in OSCC treatment.

On the high temperature oxidation of MoSi2 particles with boron addition

Boron doped MoSi2 particles have been envisioned as sacrificial particles for self-healing thermal barrier coatings (TBCs) but their oxidation behaviour is yet not well understood. In this work, oxidation of MoSi2 based particle is studied in the temperature range of 1050–1200 °C. The oxidation proceeds from a transient to a steady-state oxidation stage. The kinetics during steady-state oxidation is captured with a thermal diffusion-based model. As compared to the oxidation of pure MoSi2 particles, the addition of boron strongly enhances the silica formation. Also, a finer dispersion of MoBx in the MoSi2 matrix accelerates the formation of silica. The oxide growth rate constant increases proportional with the boron content of the MoSi2 particles. This enhanced oxidation is related to the microstructure of the oxide scale. Upon oxidation, boron yields B2O3, which promptly merge with SiO2 to form amorphous borosilicate, hindering the formation of crystalline SiO2. Consequently, the migration of oxygen in the borosilicate oxide scale is faster than in the silica oxide scale on pure MoSi2 particles.

Geochemical Specifications for Raw Materials Used in Gasin Cement Factory in Kurdistan Region Ne-Iraq

This paper intends to provide background information on the chemically investigated raw materials used in the cement industry at the Gasin Cement Factory. Since it was found that the average carbonate ratio of CaCO3 is 89.84 percent by weight ratio, the sulfide is less than 1 percent by weight ratio, and the magnesium carbonate is less than 3 percent, the raw materials entering the factory, including limestone, clay, iron, sand, and gypsum, were examined. Magnesium carbonate was less than or equal to 3 percent, in the iron with sand mixture, and the overall mixture carbonates were less than or equal to 76.24 percent. The findings of the analysis for silica oxides in the sand were greater than 82 percent. For sulfide oxide less than 1%, as well as for iron, the average value of ferric oxide that was examined in a laboratory was 35.51percent, from local iron ore, and an average reached 50.66% from Iranian iron ore, the percentage of alumina oxide that was tested in a laboratory was 9.37 percent and 3.40 percent from Local iron and Iranian iron respectively, silica oxide is more than 8.3 percent. As well as gypsum analysis, it was discovered that the average percentage of sulfur dioxide is higher than 40.97%. We identified the locations of the models that were evaluated and analyzed, as well as their storage locations.

Optoelectronic and gamma ray attenuation properties of ore-based Bi and Sn-doped borosilicate glasses

Progress in glass science has given rise to innovative functional glasses, unlocking significant applications for creating cutting-edge materials such as solid-state batteries, solar cells, optical reinforcement, and medical technologies. In this study, rice husk silica, Bismuth (Bi) and Tin (Sn) oxide ores were used to fabricate a novel glass series. The electrical conductivity (i.e., dielectric constant) of the glasses increased with the dopant's gravimetric levels. The novel glass series also possesses good optical non-linearity with metallisation criteria ranging from 0.35 to 0.40, which points to a novel non-linear optical material. The non-bridging oxygen content in the new glasses exceeds the bridging oxygen, indicating high polarisation. The transmission coefficient decreased with increasing dopant concentration from 0.76 to 0.75, while the reflection loss decreased from 0.37 to 0.38. For the Caesium-137 energy, GS6 has a minimum HVL of ∼5.02 cm, which is ∼20 % lower than that of commercial Pb/Ba glass. For the two energies, GS6 has the least MFP, suggesting that the addition of dopants improved the efficiency of the glass attenuation. Process capability analysis based on Caesium-137 (661.7 keV) and overall performance analysis of the fabricated glass series revealed that GS3 glass (15 wt% dopant) is the optimal material, even outperforming the commercial Pb/Ba glass. Although Cobalt-60 (1253 keV) yielded comparable outcomes, concentrations beyond 15 wt% in GS3 showed marginal enhancements in the photon attenuation parameters of the glasses. Hence, the fabricated GS3 and the circular synthesis method of the glasses are cost-effective for low-energy gamma/X-ray shielding. The percentage deviation between the experimental data for MAC and that of Monte Carlo simulations for Cs-137 and Co-60 energies are both within 10 %, which validates the methods of this paper.

Engineering Waveguide Nonlinear Effective Length via Low Index Thin Films

AbstractNovel photonic nanowires are fabricated using low‐index materials and tested in the near‐infrared spectrum to assess their nonlinear optical properties. In this work, the need to redefine the standard nonlinear figure of merit in terms of nonlinear phase shift and optical transmission for a given propagation distance is argued. According to this new metric, the devices largely outperform all established platforms for optical modules with a linear footprint in the range of 50–500 µm, which is demonstrated to be an outstanding technological gap. For 85 fs pulses, with carrier wavelength at 1480 nm and sub‐µW power levels, a spectral broadening exceeding 80% of the initial bandwidth was recorded over a propagation length of just 50 µm. Leveraging on CMOS‐compatible processes and well‐established materials such as silicon, silica, and indium tin oxide, the devices bring great promise for developing alternative all‐optical devices with unparalleled nonlinear performances within the aforementioned range.

Morphological Characteristics and Mechanical Properties of Quarry Dust Waste as Sand Replacement in Mortar

The generation of industrial waste has been steadily increasing, necessitating sustainable waste management strategies. Quarry dust, a by-product of the aggregate production process obtained from crushing rocks in rubble crusher units, contributes to this waste stream. This study proposes using fine quarry dust waste, ranging from 50 to 100 μm, as an additive or replacement in mortar to mitigate environmental and health hazards caused by this kind of waste. However, studies on the usage of very fine quarry dust waste (about 50-100μm particle sizes) as a partial sand replacement in mortar production is very limited. Therefore, this paper presents an experimental investigation on the effects of incorporating quarry dust waste as a sand replacement, with variations of 0%, 5%, 10%, 15%, 20%, 25%, and 30%, with a water-cement ratio of 0.5 to enhance mortar strength. The micro-structural analysis and compression tests were performed to evaluate the mortar samples. XRF analysis confirmed that silica oxide (SiO2) was the predominant element present in quarry dust waste. The compression tests were conducted on 50 mm x 50 mm x 50 mm mortar cubes. The tests were performed at 3, 7, 14, and 28-day intervals. The results revealed that, incorporating 25% quarry dust waste as a sand replacement produced the highest compressive strength of about 37 MPa on the 28th day curing duration. Hence, using this material asan environment-friendly sand replacement offers a promising solution for producing high-strength mortar. This finding highlights the potential of quarry dust waste as a supplemental cementitious material and emphasizes its viability in reducing the environmental impact associated with industrial waste.