Zirconia Research Articles

One-pot synthesis of transition metals-doped LiAl-LDHs to improve lithium adsorption performance and stability

Transition metal doping of Li/Al-LDHs can alter the interlayer spacing and surface charge of LDHs, thereby enhancing adsorption performance and stability. To investigate the rules and mechanisms governing the enhancement of stability and adsorption capacity of Li/Al-LDHs through transition metal element doping, several transition metal elements (Co, Zn, Mn, Zr, and Ni) were selected, and the five types of transition metal-doped Li/Al-LDHs and one undoped Li/Al-LDHs were synthesized by a one-pot method. Compared to the original Li/Al-LDHs, the Co-doped Li/Al-LDHs exhibited higher adsorption capacity, lower dissolution loss, and greater stability. Additionally, after Co doping, the lattice constant of Li/Al-LDHs decreases, effectively reducing the intercalation energy and increasing lithium diffusion efficiency. When used for lithium adsorption, Co-Li/Al-LDHs exhibited a Li+ capacity of 12.6 mg/g and reached saturation adsorption within 90 min. Notably, Co-Li/Al-LDHs achieved a high Li+ adsorption capacity (6.46 mg/g) in East Taigener salt-lake brine. After 10 cycles, the adsorption capacity did not show any significant change, and after 336 h adsorption-desorption cycles (200 rmp, oscillation), the total Al dissolution loss was only about 0.035 ‰, demonstrating that Co doping can enhance the interlayer binding force of Li/Al-LDHs, thereby reducing the decomposition of the layered structure in solution, lowering aluminum dissolution loss, and improving structural stability. The results show that doping with transition metals can reduce the Al dissolution rate of LDHs, and Co-Li/Al-LDHs can be used as an efficient adsorbent for lithium extraction from salt lake and have higher stability.

Development of silicone-based phantoms for biomedical optics from 400 to 1550 nm

This work describes the development of silicone-based evaluation phantoms for biomedical optics in the wavelength range from 400 to 1550 nm. The absorption coefficient μa and the reduced scattering coefficient μs′ were determined using an integrating sphere setup. Zirconium dioxide pigments were used as scatterers and carbon black as absorbers. We developed an in-house manufacturing process using a Hauschild SpeedMixer to ensure reproducibility. A set of nine cubic phantoms with three different reduced scattering and absorption coefficients was produced. Prediction of the μa and μs′ was done by using the weighted mass concentrations of the used materials. The average prediction accuracy over all wavelengths and phantoms is 1.0% for the reduced scattering coefficient and 3.5% for the absorption coefficient.

Igniting a greener future by flame synthesized zirconium oxide nanoparticles through dye adsorption

Igniting a greener future by flame synthesized zirconium oxide nanoparticles through dye adsorption

Sublimation and Recrystallization of CsPbBr3 Constructing a Perovskite-Carbon Interface to Facilitate Hole Transfer in Printable All-Inorganic Perovskite Solar Cells.

All-inorganic perovskite solar cells (APSCs) are a promising photovoltaic technology due to their unique physical and optical properties. For printable all-inorganic perovskite solar cells, the key factors limiting their photoelectric conversion performance are the crystallization of perovskite and the hole collection capability at the perovskite-carbon interface. In this study, leveraging the high-temperature tolerance of CsPbBr3 perovskite, the sublimation and recrystallization processes were controlled, significantly improving the crystalline quality of the perovskite and suppressing the generation of the nonphotovoltaic CsPb2Br5 phase. Furthermore, a continuous distribution of high-quality CsPbBr3 crystals was achieved at the interface between the carbon electrode and the zirconium oxide layer, ensuring efficient collection of photogenerated holes. The photoelectric conversion efficiency of the printable mesoscopic all-inorganic perovskite solar cell was increased from 5.04 to 8.34% (with a record value of 10.04%) and achieved an ultrahigh open-circuit voltage of 1.54 V due to the significant improvement in the crystal quality of CsPbBr3. This study proposes a novel strategy to enhance the photovoltaic conversion performance of carbon-based all-inorganic perovskite solar cells by suppressing the presence of nonphotovoltaic phases.

A hybrid MAPbI3/PEDOT-ZrO2 perovskedot composite for enhanced stability and charge transport in photo-batteries

Designing flexible photo-batteries that are capable of charged directly by light is critical for improving off-grid power options. This paper presents a unique photo-battery design that uses a MAPbI3/PEDOT as the effective light-harvesting and hole-transporting layer, and zirconium oxide (ZrO2) as the channel for electrons and hole-blocking layer. The MAPbI3 perovskite material absorbs sunlight and develops charge carriers, while PEDOT helps transport holes to the anode, improving charge separation and minimizing recombination losses. ZrO2, with its strong electron mobility and great chemical stability, provides fast transport of electrons to the cathode. It also efficiently blocks holes, increasing overall charge transfer dynamics. This improved design improves photo-conversion efficiency by up to 0.51 % and has a high capacity retention rate of around 96 % after 500 cycles. This improved MAPbI3/PEDOT/ZrO2 photo-battery could decrease light charging time by three times, enabling adaptable, light-rechargeable batteries more practical for real-world applications.

Development of laser felling modes of gas-thermal coating

The use of copper and its alloys to create parts for metallurgical equipment is associated with an increase in abrasive wear and high-temperature corrosion. In this regard, there is a need to apply a protective coating. In particular, to prevent wear and premature chipping of the metal of copper tuyeres, the surface is hardened with a coating of zirconium dioxide stabilized with yttria oxide by thermal spraying in an air atmosphere. Due to the difference in the coefficient of thermal expansion of copper (at T = 300 K: 16.7 µm/m оС and at T = 750 K: 19.7 µm/m оС) and its low resistance to gas corrosion, the application of zirconium oxide (produced by a preapplied intermediate layer that plays a role in matching the coefficient of thermal expansion (CTE) between the copper base and the ceramic coating. In addition, the intermediate layer protects copper from gas corrosion. In this case, The use of copper and its alloys to create parts for metallurgical equipment is associated with an increase in abrasive wear and high-temperature corrosion. In this regard, there is a need to apply a protective coating. In particular, to prevent wear and premature chipping of the metal of copper tuyeres, the surface is hardened with a coating of zirconium dioxide stabilized with yttria oxide by thermal spraying in an air atmosphere. Due to the difference in the coefficient of thermal expansion of copper (at T = 300 K: 16.7 pm/m °G and at T = 750 K: 19.7 pm/m оG) and its low resistance to gas corrosion, the application of zirconium oxide (produced by a pre-applied intermediate layer that plays a role in matching the coefficient of thermal expansion (CTE) between the copper base and the ceramic coating. In addition, the intermediate layer protects copper from gas corrosion. In this case, nickel-based alloys were used as intermediate layers. The use of nickel as the basis of intermediate layers is due to the fact that copper and nickel form a continuous series of solid solutions, such as cupronickel or monel metal-like structures. This, in turn, assumes a smooth transition of thermophysical properties from copper to nickel alloy. To ensure increased adhesion of the transition layer to copper by increasing the area of mutual contact between copper and the sublayer (dagger penetration) and significantly increasing the homogeneity of the material of the intermediate layer made of a nickel alloy, laser melting of the intermediate sublayer (Ni–B–Si system) was used on a laser complex based on laser LS-5 with a power of 5 kW with a KUKA KR-60HA robot in an argon atmosphere. To test the modes, experiments were carried out on copper samples of a flat shape and a body of rotation. The optimal parameters for the process of melting flat samples were: processing speed 33 mm/s, power from 400 to 3900 W, focal length from 200 to 230 mm, pitch between tracks: 0.25, 0.5 and 1 mm. The optimal parameters for the process of melting rotating samples were: laser radiation power 400–450 W, processing step 0.125; 0.5, focal length from 200 to 210 mm.

The Role of Oxygen Vacancy on the Carbon Dioxide Photoreduction Using Monoclinic and Tetragonal-phase Zirconium Oxide

The Role of Oxygen Vacancy on the Carbon Dioxide Photoreduction Using Monoclinic and Tetragonal-phase Zirconium Oxide

Stabilization of Tetragonal Phase in Hafnium Zirconium Oxide by Cation Doping for High-K Dielectric Insulators.

As electronic circuit integration intensifies, there is a rising demand for dielectric insulators that provide both superior insulation and high dielectric constants. This study focuses on developing high-k dielectric insulators by controlling the phase of the Hf0.5Zr0.5O2 (HZO) film with additional doping, utilizing yttrium (Y), tantalum (Ta), gallium (Ga), silicon (Si), and aluminum (Al) as dopants. Doping changes the ratio of tetragonal to monoclinic phases in doped HZO films, and Y-doped HZO (Y:HZO) films specifically exhibit a high tetragonal phase ratio and a dielectric constant of 40.9, indicating superior insulating properties compared to undoped HZO films. To clarify the fundamental mechanism driving the enhancement in dielectric properties, we have carried out various analyses combined with density functional theory (DFT) calculations. Through the optimization of the post-deposition annealing (PDA) process and the heterojunction structure with Al2O3, an Al2O3/Y:HZO heterojunction with a high dielectric constant and even lower leakage current compared to a single layer was developed. The thin-film transistor (TFT) with the Au/Ti/amorphous InGaZnO4 (a-IGZO)/Al2O3/YHZO/TiN heterojunction structure exhibits low subthreshold swing (SS) values within a narrow gate-source voltage (Vsg) range. This study advances knowledge on how the controlled-phase doped HZO films affect the dielectric constant and leakage current and will contribute to semiconductor technology advancements by overcoming the limitations of conventional high-k dielectric insulators.

Alternative Treatments for Zirconium Oxide to Compare Commonly Used Surface Treatments to Determine Which Has the Least Effect on the Phase Transformation.

Traditional mechanical processing of zirconium leads to an unfavorable transformation, from a metastable tetragonal phase to a monoclinic phase (t→m), which weakens the structure of the material and subsequently leads to damage to the prosthetic restoration. The aim of this research is to compare commonly used surface treatments to determine which has the least effect on t→m. Thirty cylindrical samples made of sintered zirconium were divided into six groups based on the following treatments: polishing, grinding, sandblasting, chemical etching, laser structuring or dry plasma etching. After surface treatment, the samples were subjected to the following tests: X-Ray Diffraction, microscopic examination, surface wettability and surface roughness measurements. Chemical etching, laser structuring and plasma etching significantly reduce the content of the monoclinic phase. All surface treatments significantly reduced the final amount of the monoclinic phase. However, chemical etching did not provide sufficient surface roughness. Both laser and plasma processing offer the advantage of creating structural patterns on the surface of elements. However, as plasma etching requires a mask to obtain the appropriate pattern on the surface, it seems that laser processing offers more and varied structuring possibilities. Laser structuring is easier to control and more economical than the other methods.

Green synthesis of quercetin-coated ecofriendly Zirconium oxide nanoparticles and evaluating its in vitro biological activities

Green synthesis of quercetin-coated ecofriendly Zirconium oxide nanoparticles and evaluating its <i>in vitro</i> biological activities

Analog reservoir computing via ferroelectric mixed phase boundary transistors

Analog reservoir computing (ARC) systems have attracted attention owing to their efficiency in processing temporal information. However, the distinct functionalities of the system components pose challenges for hardware implementation. Herein, we report a fully integrated ARC system that leverages material versatility of the ferroelectric-to-mixed phase boundary (MPB) hafnium zirconium oxides integrated onto indium–gallium–zinc oxide thin-film transistors (TFTs). MPB-based TFTs (MPBTFTs) with nonlinear short-term memory characteristics are utilized for physical reservoirs and artificial neuron, while nonvolatile ferroelectric TFTs mimic synaptic behavior for readout networks. Furthermore, double-gate configuration of MPBTFTs enhances reservoir state differentiation and state expansion for physical reservoir and processes both excitatory and inhibitory pulses for neuronal functionality with minimal hardware burden. The seamless integration of ARC components on a single wafer executes complex real-world time-series predictions with a low normalized root mean squared error of 0.28. The material-device co-optimization proposed in this study paves the way for the development of area- and energy-efficient ARC systems.

Non-Equal Contributions of Different Elements and Atomic Bonds to the Strength and Deformability of a Multicomponent Metallic Glass Zr47Cu46Al7.

Multicomponent metallic glasses (MGs) are a fascinating class of advanced alloys known for their exceptional properties such as limit-approaching strength, high hardness and corrosion resistance, and near-net-shape castability. One important question regarding these materials that remains unanswered is how the different elements and atomic bonds within them control their strength and deformability. Here, we present a detailed visual and statistical analysis of the behaviors of various elements and atomic bonds in the Zr47Cu46Al7 (at%) MG during a uniaxial tensile test (in the z-direction) simulated using molecular dynamics. Specifically, we investigate the identities of atoms undergoing significant shear strain, and the averaged bond lengths, projected z-lengths, and z-angles (angles with respect to the z-direction) of all the atomic bonds as functions of increasing strain. We show that, prior to yielding, the Zr element and the intermediate (Zr-Zr, Cu-Al) and stronger (Zr-Al, Zr-Cu) bonds dominate the elastic deformation and strength, while the Cu and Al elements and the weaker Al-Al and Cu-Cu bonds contribute more to the highly localized shear transformation. The significant reconstruction, as signified by the cessation of bond-length increment and bond-angle decrement, of the intermediate and the stronger bonds triggers yielding of the material. After yielding, all the elements and bonds participate in the plastic deformation while the stronger bonds contribute more to the residual strength and the ultimate (fracture) strain. The results provide new insights into the atomic mechanisms underlying the mechanical behavior of multicomponent MGs, and may assist in the future design of MG compositions towards better combination of strength and deformability.

Construction and Properties of Ultralow Thermal Conductivity and High Strength Zirconia Aerogel Composites by Freeze-Drying.

Zirconia aerogels possess significant applications, including their use catalyst carriers, thermal insulation materials, and thermal barrier coatings. This is due to their ultrahigh temperature resistance, high porosity, and low thermal conductivity. Nonetheless, the inherent challenges associated with ZrO2 aerogels, such as high brittleness, low compressive strength, and inadequate formability, restrict their potential applications. In this paper, with ultralow thermal conductivity and high strength zirconia aerogel composites with inorganic zirconium salt zirconium carbonate as the raw material, acetic acid as the solvent, polyvinylpyrrolidone (PVP) as the viscosity builder to stabilize the structure of the aerogel during the freeze-drying process. Additionally, yttrium nitrate hexahydrate (Y(NO3)3·6H2O) is employed as a phase stabilizer. The sol-gel method, in conjunction with the freeze-drying process, is utilized to fabricate ZrO2 aerogel composites with an optimized microstructure. The findings indicate that optimal process parameters are achieved with a PVP solution concentration of 2.0 wt % and a zirconium carbonate concentration of 20 wt %. The mechanical properties of the resulting composites reach up to 550 kPa, while the thermal insulation performance exhibits a temperature difference of 207 °C/cm and a thermal conductivity of 0.0504 W/(m·K). This advancement addresses the mechanical stability issues commonly associated with traditional ceramic aerogels and widely used elastic insulating materials, thereby enhancing their applicability as thermal insulation and heat preservation materials.

Experimental Research on Basalt Fabric-Based Composites for Protection Against Contact Heat

ABSTRACT The unique properties of basalt fibers, i.e. low thermal conductivity, thermal resistance up to 800°C, biodegradability, resistance to acids and alkalis, corrosion, ultraviolet radiation, and non-flammability, make them increasingly used in personal protective equipment. The design and production of basalt fabric-based composites were performed, and composite layers were directly modified by depositing thin coatings using the magnetron sputtering method. The designing and testing were performed in five stages. For direct basalt fabric modification and basalt fabric-based composites, resistance to contact heat was tested for contact temperatures of 100°C and 250°C. Moreover, the uncertainty budgets of the threshold time measurement results were determined and analyzed for all composites. New basalt fabric-based composites were designed to protect users from contact heat in hot work environments. As a result of the research, it was found that applying composite coatings: aluminum and zirconium dioxide or aluminum and zirconium dioxide and titanium dioxide to both composite layers proved to be effective in obtaining composites that guarantee perfect resistance to contact heat up to 250°C.

The Application of TiO2/ZrO2-Modified Nanocomposite PES Membrane for Improved Permeability of Textile Dye in Water.

This study investigates the modification of polyethersulfone (PES) membranes with 1 wt% titanium dioxide (TiO2), zirconium dioxide (ZrO2) and a nanocomposite of TiO2/ZrO2. The aim was to efficiently remove Rhodamine B (RhB) from water using a threefold approach of adsorption, filtration and photodegradation. Among the modified membranes (TiO2, ZrO2 and TiO2/ZrO2), the TiO2/ZrO2-PES nanocomposite membrane showed a better performance in rejection of RhB than other membranes with the rejection efficiency of 96.5%. The TiO2/ZrO2-PES membrane was found to possess a thicker selective layer and reduced mean pore radius, which contributed to its improved rejection. The TiO2/ZrO2 nanocomposite membrane also showed high bulk porosity and a slightly lower contact angle of 69.88° compared to pristine PES with a value of 73°, indicating an improvement in hydrophilicity. Additionally, the TiO2/ZrO2-PES nanocomposite membrane demonstrated a relatively lower surface roughness (Sa) of 8.53 nm, which offers the membrane antifouling properties. The TiO2/ZrO2-PES membrane showed flux recovery ratio (FRR), total fouling (Rt), reversible fouling (Rr) and irreversible fouling (Rir) of 48.0%, 88.7%, 36,8% and 52.9%, respectively. For the photocatalytic degradation performance, the removal efficiency of RhB followed this order TiO2 > TiO2/ZrO2 > ZrO2 (87.6%, 85.7%, 67.8%). The tensile strength and elongation were found to be compromised with the addition of nanoparticles and nanocomposites. This indicates the necessity to further modify and optimise membrane fabrication to achieve improved mechanical strength of the membranes. At low pressure, the overall findings suggest that the TiO2/ZrO2 nanocomposite has the potential to offer significant improvements in membrane performance (water flux) compared to other modifications.

Role of Mo and Zr Additions in Enhancing the Behavior of New Ti–Mo Alloys for Implant Materials

AbstractThe utilization of Ti–Mo alloys in biomedical applications has gained attention for use in biomedical applications owing to their non-toxicity, reasonable cost, and favorable properties. In the present study, Ti–12Mo–6Zr and Ti–15Mo–6Zr alloys were prepared using elemental blend and mechanical alloying techniques. The effect of alloying elements Mo and Zr of Ti–Mo alloy, as well as the effect of fabrication techniques of Ti–Mo–Zr trinary alloys, were investigated. Thermodynamic calculations supported by CALPHAD analysis revealed that the addition of Zr increases lattice distortion, which contributes to enhancing the strength. Conversely, adding Mo decreases the enthalpy, facilitating improved mixing and solid solution formation. The as-sintered samples were characterized by X-ray diffraction, optical microscope, and scanning electron microscopy, and their microhardness, compressive, and corrosion behavior were investigated. Among all the investigated alloys, Ti–15Mo–6Zr alloy prepared by the mechanical alloying technique, milled for six hours at 300 rpm, compacted at 600 MPa, and sintered at 1250 ℃, shows good comprehensive mechanical properties with a preferable compressive strength (− 1710 MPa) and hardness (396 HV5), as well as the lowest wear rate (0.69%) and corrosion rate (0.557 × 10–3 mm/year). This can be related to the solid solution strengthening and relative density, together with dispersion and precipitation strengthening of the α phase. Remarkably, the combination of high mechanical and corrosion properties can be achieved by tailoring the content of the α phase, controlling the density, and providing new fabricating techniques for β Ti alloys. Graphical Abstract

Serpentinised Dunites of the Neoarchean Shimoga Greenstone Belt, Western Dharwar Craton, India: Insights on Ni‐PGE Mineralisation and Genesis

ABSTRACTUltramafic rocks of the Archean greenstone belts worldwide are potential hosts for Cu‐Ni, precious metal deposits like platinum group elements (PGEs) and gold. This study highlights the geochemical evidence and genesis of Ni‐PGE mineralisation in the ultramafic rocks of Shimoga greenstone belt of the Western Dharwar Craton, India. Petrographically, the studied rocks are identified to be serpentinised dunites, while their geochemical signatures indicate komatiitic affinity. Presence of disseminated sulphides and pronounced serpentinisation in these rocks suggest a combination of Type II (disseminated sulphides) and Type IV (post‐magmatic alterations) komatiite‐related Ni–Cu‐PGE deposits. Chondritic Al2O3/TiO2 (9.65–16.38) ratios, superchondritic Gd/YbN (1.3–1.6), depleted high‐field‐strength elements (HFSEs) (Zr, Hf), enrichment of LREE over HREE and negative Nb–Ta anomalies reflect the generation of parental melts from plume‐sourced Al‐depleted komatiites with significant crustal contamination during their emplacement. The major, trace element and PGE relationships (FeO vs. MgO, Cu vs. Pd, Ni/Cu vs. Pd/Ir) infer the origin of sulphur undersaturated primary melts through moderate to higher degrees of partial melting followed by crustal assimilation that led to PGE enrichment. These observations suggest their formation from melts derived from greater depths of the upper mantle (&gt; 400 km) at high pressure (&gt; 10 GPa), wherein, the mantle residue retained majorite garnet. The high Ni (avg. Ni = 6511 ppm) substantiated by high Kambalda ratio ([Ni:Cr] × [Cu:Zn] = 5.6), Ni/Cr ratios (&gt; 1) with high concentration of PGEs (avg. ∑PGE = 3078 ppb) confirm the fertile/mineralised nature of the komatiitic source and potential Ni‐PGE mineralization in the ultramafic rocks of the Shimoga greenstone belt.

Assessment of surface hardness and impact strength of denture base resins reinforced with silver–titanium dioxide and silver–zirconium dioxide nanoparticles: In vitro study

Abstract Polymethyl methacrylate (PMMA) is frequently utilised for fabricating denture bases due to its perfect qualities. However, a significant issue with this resin is the occurrence of frequent fractures caused by heavy chewing power, resulting in early cracks and fractures during clinical use. This study investigates the influence of silver, titanium dioxide, and silver zirconia nanoparticles on the surface hardness and impact strength of self-cured denture base. The samples were categorised into four categories according to the incorporation of different nanoparticles. The samples were divided into three subgroups based on the nanoparticle content: 0.1, 0.3, and 0.5% of TiO2 and ZrO2. Each group had a set ratio of 0.3% Ag as an antibacterial agent. Except for the fourth group (Group D), a combination of 0.05, 0.15, and 0.25% of TiO2 and ZrO2, along with 0.3% Ag, was utilised to investigate their collective impact. The Shore D hardness and Charpy test were employed to quantify the surface hardness and impact strength, respectively. The samples were subjected to X-ray diffraction analysis and field emission-scanning electron microscopy to characterise nanoparticles and ascertain the structure of acrylic samples. All nanoparticle-modified samples showed a substantial improvement in surface hardness compared to the control group. The maximum hardness value was seen in the samples containing 0.3% Ag–0.3% TiO2 and 0.3% Ag–0.5% ZrO2. The samples treated with 0.3% Ag and 0.3% TiO2 showed the maximum impact strength. The incorporation of Ag and ZrO2 hinders the ability to withstand impact strength. The samples treated with 0.3% Ag, 0.15% TiO2, and 0.15% ZrO2 exhibited an augmentation in impact strength. Modified samples in all groups showed a colour change, which required colour modifiers.

Synthesis of heterogeneous nanocomposite catalyst ZrO2@SBA-15 for formic acid production from hemicelluloses

Heterogeneous nanocomposite ZrO2@SBA-15 catalysts containing 10 wt. % of zirconium oxide were synthesized by two methods: co-condensation and incipient wetness impregnation. The silica support and catalysts were characterized by X-ray diffraction, gas adsorption, FTIR-spectroscopy and other physicochemical methods. As a result of zirconia introduction into the silica wall, the mesostructured of SBA-15 is preserved, but the specific surface area and pore Volume are reduced. It was established that during one-stage co-condensation synthesis, the particle fibers shorten and stick together. The catalysts were tested in the process of catalytic hydrolysis-oxidation of hemicelluloses of aspen wood. The optimal formic acid synthesis conditions were determined: 150°С, 3 h. The highest formic acid yield obtained over the catalyst obtained by co-condensation under best reaction conditions was 28.4 wt. %.

Synthesis of magnetic zirconium oxide-iron oxide nanoparticles composite using chemical precipitation process for Pb (II) adsorption

The exploration and utilization of natural raw zircon minerals in Indonesia, particularly in Central Kalimantan, remain largely untapped in their potential as high-tech and commercially valuable substances with eco-friendly properties, particularly in water and industrial wastewater treatment. The primary objective of this research is to enhance the development and synthesis of natural raw zircon minerals by converting them into zirconium oxide and integrating them with magnetic nanoparticles. The magnetic nanoparticle composite material for zirconium oxide (MNP@ZrO2) was synthesized using the chemical co-precipitation method. Zirconium and its oxides have gained significant application in water and wastewater treatment in recent years. Through chemical co-precipitation processes (MNP@ZrO2), the natural raw zircon minerals were transformed into zirconium oxides and combined with magnetic nanoparticles due to their exceptional potential as effective adsorbents for anions and cations in water and industrial treatment processes. In the utilization of Scanning Electron Microscopy (SEM), magnetic nanoparticles with a diameter of less than 50 nm emerged on the surface of the zirconium crystals within the magnetic nanoparticle composites. X-ray diffraction (X-RD) analysis indicated that the treatment of zirconium minerals resulted in 11.19% decrease in the Crystallinity Index and a significant reduction of 98% in silica content. By maintaining a pH level of approximately 7 ± 0.2 over 360 min with a stirring rate of 150 rpm, and at ambient temperature, the optimal conditions for Pb (II) adsorption were achieved with the adsorption capacity of 68.98 mg/g using MNP@ZrO2 as adsorbent. The successful synthesis of magnetic zirconium oxide-iron oxide nanoparticles at various pH levels using the chemical co-precipitation process has facilitated a comprehensive assessment of their performance in Pb (II) adsorption.