ZrO2 Nanoparticles Research Articles

Densification of hydroxyapatite/zirconia nanocomposites fabricated via low-temperature mineralization sintering process and their mechanical properties

Hydroxyapatite/zirconia (HAP/ZrO2) composites were fabricated via the low-temperature mineralization sintering process (LMSP) at an extremely low temperature of 130 °C to enhance the mechanical properties of HAP and broaden its practical applications. For this purpose, 5–20 vol% calcia-stabilized ZrO2 were introduced into HAP, and HAP/ZrO2 nanoparticles, mixed with simulated body fluid, were densified under a uniaxial pressure of 800 MPa at 130 °C. At 10 vol% ZrO2, the relative density of the HAP/ZrO2 composite was determined to be 88.3 ± 1.1%. Additionally, it exhibited the highest values of mechanical properties such as the Vickers hardness (3.68 ± 0.18 GPa), fracture toughness (1.11 ± 0.10 MPa·m1/2), biaxial flexural strength (63.72 ± 2.35 MPa), and Young’s modulus (83.91 ± 1.93 GPa) among the composite samples. These values were considerably higher than those of the pure HAP matrix due to the adequate reinforcement by ZrO2 nanoparticles. Notably, owing to the low sintering temperature, phase decomposition of HAP, normally observed at high sintering temperatures above 1200 °C, was not observed. These results suggest that LMSP enables the incorporation of reinforcing ceramic materials with high sintering temperatures into bioactive materials at significantly lower temperatures, thereby improving their properties.

Enhanced wear resistance, hydrophobic properties and corrosion resistance of plasma electrolyte oxidation coatings on Ti6Al4V alloys via addition of ZrO2 nanoparticles

Enhanced wear resistance, hydrophobic properties and corrosion resistance of plasma electrolyte oxidation coatings on Ti6Al4V alloys via addition of ZrO2 nanoparticles

Effect of structural evolutions on optical and electronic properties of co-precipitated ZrO2 nanoparticles

Effect of structural evolutions on optical and electronic properties of co-precipitated ZrO2 nanoparticles

Engineered Polystyrene‐Zirconium Dioxide Nanocomposite With Enhanced Optical Properties

ABSTRACTThe demand for transparent polymers with high‐refractive indices (RIs) is increasing due to their versatility; however, low RIs also hold significance. Engineering the RI of polymer nanocomposites is crucial which benefits industry and research. The study investigates the influence of ZrO2 nanoparticles on the optical and surface properties of the polystyrene matrix. UV–Vis spectroscopy confirms that transparency is maintained with a light transmittance of 90 even with a ZrO2 loading of 16 wt%, while ellipsometry shows a steady increase in the RI due to the incorporation of nanoparticles. The RI of composites exceeds that of pure polystyrene (RI: 1.3–1.7) and utilizes the RI of ZrO2 (> 2.00) without altering the sample thickness. The microscopic image shows uniform distribution of particles up to 8 wt%, with slight agglomeration at higher contents. Scanning electron microscopy examination shows that the ZrO2 nanoparticles (20–150 nm) form loose agglomerated structures, while atomic force microscopy examination shows aggregate formation at 16 wt%. The addition of ZrO2 increases the surface roughness and water contact angle up to 4 wt%, which is related to the concentration of the nanofiller and the minimal interaction between ZrO2 and water. The results demonstrate the potential of ZrO2‐loaded nanocomposites for applications requiring high RIs and optical transparency.

Green synthesis of single phase of ZrO2 nanoparticles via Sonchus asper aqueous extract: antibacterial, antioxidant, cytotoxic, and photocatalytic applications

Green synthesis of single phase of ZrO2 nanoparticles via Sonchus asper aqueous extract: antibacterial, antioxidant, cytotoxic, and photocatalytic applications

COMPARISON OF SOME MECHANICAL PROPERTIES OF ADDING ZrO2 NANOPARTICLES TO MICROWAVE-CURED ACRYLIC AND HOT-CURED DENTURE BASE ACRYLIC MATERIALS

Background: The mechanical properties of denture-base acrylic resin have declined over the past decade, it is imperative to take immediate action to investigate alternative possibilities, such as employing metal oxide nanoparticles, which have shown considerable promise in diverse applications in the fields of nanobiotechnology, specifically in biological and health care fields. Aims: Exploring the effect of incorporating zirconium oxide (ZrO2) nanoparticles into microwave-cured acrylic and hot-cured acrylic denture base materials, on the tensile strength, impact strength and structural chemical changes. Methods: A total of 66 samples were utilized. The manufacturer's instructions have been followed for the production of specimens for each product. The impact of addition 0%, 3% and 5% zirconium oxide (ZrO2) nanoparticles were examined. Results: Addition of 3% and 5% ZrO2 nanoparticles improved the tensile and impact strengths with no chemical alterations changes with the addition of ZrO2 NPs, with 3% ZrO2 showing a greater enhancement than 5%. Conclusions: Incorporating 3% ZrO2 nanoparticles into both microwave-cured and hot-cured acrylic denture base materials enhances tensile and impact strengths more effectively than 5%, with no chemical changes observed.

Modification of blend reverse osmosis membranes using ZrO2 for desalination process purposes

Desalination of water is a crucial step in the process of obtaining potable water. One of the main challenges for the researchers is its efficient application and affordable preparation. It was planned to prepare the flat sheet membranes using cellulose acetate as a base polymer, and polyvinyl alcohol (PVA) as an additive with dosing of (0.1, 0.3, 0.5, and 0.7 wt%) from zirconium oxide (ZrO2) nanoparticle. SEM, TEM, and XRD analyses were used to characterize the generated ZrO2 nanoparticle in order to confirm its nano-size and crystal structure. The surface morphologies and existence of the dense layer, which is the typical property of the RO membrane capable of salt separation, were identified on the manufactured RO membranes by SEM. Membranes prepared by embedding 0.5 wt%ZrO2 with PVA/CA proved efficient as RO membranes using 2000 ppm NaCl and exhibited high salt rejection of 97% and water permeability of 12.5 LMH. Also, there is a decrease in the NaCl removal tendency was observed with the excessive dosages of ZrO2 with 0.7 wt%, which was due to the concentration polarization, which blocks the pores on the surfaces of the membranes. The antifouling behavior of the prepared membranes was tested using bovine serum albumin (BSA), the results indicate the low irreversible resistance, total fouling resistance, and high flux recovery ratio compared to the neat membrane. The prepared membranes have a stable salt rejection and water productivity even after demonstrating with chlorine (25–100 mg l−1 of NaOCl for 120 min).

Study of morphology, phase composition, optical properties, and thermal stability of hydrothermal zirconium dioxide synthesized at low temperatures.

Oxide nanoparticles exhibit unique features such as high surface area, enhanced catalytic activity, and tunable optical and electrical properties, making them valuable to various industry applications as well as for the development of new research projects. Nowadays, ZrO2 nanoparticles are widely used as catalysts and precursors in ceramic technology. Hydrothermal synthesis with metal salts is one of the most common methods for producing stable tetragonal-phase zirconium dioxide nanoparticles. However, hydrothermal synthesis requires relatively high process temperatures (160-200°C) and the use of advanced heat-resistant autoclaves capable of maintaining high pressure. This paper investigates how different precursors (ZrOCl₂·8H₂O and ZrO(NO₃)₂·2H₂O) and synthesis temperatures (110-160°C) affect the phase composition, optical properties, size, and shape of ZrO₂ nanoparticles produced by hydrothermal synthesis without calcination. In addition, the effect of temperature exposure in the range of 100-1000°C on the phase stability of the synthesized nanoparticles was studied. X-ray diffraction and Raman spectroscopy techniques were used to determine the structure and phase composition, while the optical properties were examined through the analysis of transmission and absorption spectra in the visible and UV ranges. It was found that the obtained particles at synthesis temperatures of 110-130°C have predominantly cubic c-ZrO2 phase, which changes to monoclinic phase when heated above 500°C. Analysis of visible and UV spectroscopy data reveals that the experimental samples have pronounced absorption in the middle UV range (200-260nm) and have an energy band gap Eg varying from 4.8 to 5.1eV. The hydrothermal powders synthesized in this study can be used as absorbers in the mid-UV range and as reinforcing additives in the preparation of technical ceramics.

Evaluation of the Effect of ZrO2 Nanoparticles and Glass Fibers on the Shear Bond of Repaired Heat-Cured PMMA

Evaluation of the Effect of ZrO2 Nanoparticles and Glass Fibers on the Shear Bond of Repaired Heat-Cured PMMA

Effect of Dehydrogenation and Heat Treatments on the Microstructure and Tribological Behavior of Electroless Ni-P Nanocomposite Coatings.

High phosphorus Ni-P coatings, both unreinforced and modified by the addition of alumina (Al2O3) and zirconia (ZrO2) nanoparticles, were manufactured by electroless deposition technique and heat-treated with different temperature and duration schedules. The effect of dehydrogenation (200 °C for 2 h) and its combination with crystallization heat treatment was studied in terms of microstructural changes and wear resistance. The amorphous structure of the coatings was not altered by the introduction of both Al2O3 and ZrO2 nanoparticles, and the addition of 1.5 g/L of ZrO2 yielded the highest microhardness due to better particles dispersion. Dehydrogenation improved hardness because of the early stages of grain growth; however, the greatest improvement in hardness (+120% compared to unreinforced Ni-P) was obtained after annealing at 400 °C for 1 h, because of the microprecipitation of the Ni3P crystalline phase induced by thermal treatment. No detectable differences in hardness and microstructure were detected when annealing at 400 °C for 1 h with or without prior dehydrogenation; however, the dehydrogenated coatings exhibited a lower Young's modulus. ZrO2-reinforced coatings demonstrated improved wear resistance, and wear tests revealed that dehydrogenation is fundamental for lowering the coefficient of friction (-14%) and wear rate (-97%) when performed before annealing at 400 °C for 1 h. The analysis of the wear tracks showed that the non-dehydrogenated samples failed by complete coating delamination from the substrate, with abrasion identified as the predominant wear mechanism. Conversely, the dehydrogenated samples demonstrated better resistance due to the formation of a protective oxide layer, leading to an overall increase in the coating wear resistance.

Assessing the Different Nanoparticle-Reinforced Bonding Agents on the Shear Bond Strength of Orthodontic Brackets

ABSTRACT Background: The strength of the binding between brackets and tooth surfaces has a major impact on how well orthodontic therapy works. The shear bond strength of orthodontic brackets may be strengthened by the invention of bonding agents supplemented with nanoparticles, thanks to recent developments in nanoparticle technology. Materials and Methods: In order to perform a randomized controlled experiment, 90 human premolars were excised for orthodontic purposes. Three groups of 30 teeth were randomly assigned to each group: Group A used a bonding agent augmented with nanoparticles of titanium dioxide (TiO2), Group B used nanoparticles of zirconium dioxide (ZrO2), and Group C used a standard bonding agent as a reference. The appropriate bonding chemicals were used to attach the brackets to the teeth, and a universal testing equipment was used to measure the shear bond strength. Stereomicroscopic analysis was used to evaluate the failure mechanisms. To do statistical analysis, Tukey’s post hoc test and analysis of variance were used. Results: There were significant differences (P < 0.05) in the mean shear bond strength values across the groups. The average shear bond strength for Group A (TiO2) was 18.5 ± 2.3 MPa, that for Group B (ZrO2) was 17.2 ± 2.6 MPa, and that for Group C (control) was 14.8 ± 2.4 MPa. In comparison to Groups B and C, Group A exhibited a statistically greater bond strength, although Group B also showed an improvement over the control. According to the failure mode analysis, the control group had mostly adhesive failures, whereas the nanoparticle groups saw mixed failures. Conclusion: When TiO2 and ZrO2 nanoparticles are added to bonding agents, the shear bond strength of orthodontic brackets is greatly increased in comparison to traditional bonding agents. TiO2-reinforced materials performed better, pointing to possible benefits for orthodontic applications. It is advised that further study be done to examine the long-term impacts and therapeutic implications of these results.

Facile constructing ZrO2 nanoparticles equipped with high conductivity carbon networks as pseudocapacitive anodes for removing phosphorus

Phosphorus pollution can seriously disrupt water quality and endanger ecosystem sustainability. Nonetheless, a few typical methods have been employed to remove phosphorus, but there are still challenges in controlling phosphorus from sewage. Capacitive deionization (CDI) displays the merits of having eco-friendliness and low energy consumption when capturing phosphorus. However, traditional carbon electrodes often suffer from the limitation that phosphorus uptake sites are insufficient. Herein, a novel ZrO2 nanoparticle equipped with a highly conductive carbon network (NZrC) was fabricated by a facile co-pyrolysis process. Na2EDTA can provide additional carbon backbones, N species, and metal chelation sites. Zr-MOF was applied as the ZrO2 precursor with abundant phosphorus trapping sites. The results suggested that Na2EDTA favors improving the ZrO2 dispersion, mesoporous channel formation, and pseudocapacitive behavior. NZrC-21 at 1.2 V displays low energy consumption and the optimal phosphorus uptake capacity of 10.99 mg P/g because of its rich mesoporous structure, abundant pyrrolic-N, graphitic-N, and ZrO2 active sites, and outstanding electrochemical properties. Furthermore, several key parameters were investigated for their effect on phosphorus removal performance. The mechanism revealed that hydrogen bonds, ligand exchange, and electrostatic attraction are the main uptake processes. This work presents a novel perspective for the facile construction and utilization of metal oxide nanoparticles equipped with a highly conductive carbon network for removing phosphorus.

Photocatalytic rice bran protein/carboxymethyl cellulose/ZrO2 fiber produced by microfluidics: Formation mechanism, bacteriostasis and strawberry preservation

Developing cost-effective and environmentally sustainable active packaging materials remains an important challenge. We have developed rice bran protein (RBP)-based fibers incorporating carboxymethyl cellulose (CMC) and ZrO2 nanoparticles (ZrO2 NPs, 0 %–7 %, m/m) using microfluidic spinning. The integration of RBP, CMC, and ZrO2 NPs formed a robust hydrogen bond network that enhanced the fibers' thermal stability and crystallinity, reduced surface hydrophobicity, and aligned the molecular orientation. Under the catalysis of visible light (300 W, 12 h), ZrO2 NPs in the fiber produced reactive oxygen species, which inhibited the oxidative stress resistance system of Bacillus subtilis and destroyed its biofilm and DNA, thus showing excellent antibacterial effect. Additionally, during storage, this fiber also showed the ability to scavenge ethylene, thereby reducing the rate of loss of luminance, hardness and weight of strawberries. This study offers a new idea for RBP fiber in food preservation, antibacterial, and value-added utilization of rice bran by-products.

Simultaneous improvement of wear and corrosion resistance of microarc oxidation coatings on ZK61 Mg alloy by doping with ZrO2 nanoparticles

The poor corrosion resistance of magnesium (Mg) and its alloys limits their application in various fields. Micro arc oxidation (MAO) coatings can improve the corrosion resistance, but the pore defects and low surface hardness make them susceptible to wear and accelerated corrosion during usage. In this study, a ZrO2 nanoparticles doped-MAO coating is prepared on the ZK61 Mg alloy by utilizing an MgF2 passivation layer to prevent ablation. The ZrO2 nanoparticles re-melt and precipitate due to local discharging, which produces evenly dispersed nanocrystals in the MAO coating. As a result, the hardness of the MAO coating with the appropriate ZrO2 concentration increases by over 10 times, while the wear rate decreases and corrosion resistance increases. With increasing ZrO2 concentrations, the corrosion potentials increase from −1.528 V of the bare ZK61 Mg alloy to −1.184 V, the corrosion current density decreases from 1.065 × 10–4 A cm–2 to 3.960 × 10–8 A cm–2, and the charge transfer resistance increases from 3.41 × 102 Ω cm2 to 6.782 × 105Ω cm2. Immersion tests conducted in a salt solution for 28 d reveal minimal corrosion in contrast to severe corrosion on the untreated ZK61 Mg alloy. ZrO2 nanoparticles improve the corrosion resistance of MAO coatings by sealing pores and secondary strengthening of the corrosion product layer.

Physicochemical, optical and magnetic properties of ZrO2/Fe2O3 nanocomposite and its application in photocatalysis and antibacterial treatment

In this work ZrO2/Fe2O3 nanocomposite was synthesised through hydrothermal method using an innovative approach. X-ray diffraction (XRD) analysis revealed the formation of tetragonal ZrO2 and α-Fe2O3 in the nanocomposite. The FTIR spectra of the prepared samples exhibited characteristic peaks corresponding to ZrO2 and Fe2O3 and UV–Visible spectroscopy reveals that the nanocomposite exhibits a significantly lesser bandgap than the pure nanoparticles as determined by the Kubelka Munk function used for bandgap computation. Photoluminescence analysis substantiates the reduction in the recombination rate in the ZrO2/Fe2O3 nanocomposite as compared to the pure ZrO2 nanoparticles. Reduction in the bandgap as well as the recombination rate makes the nanocomposite favourable in the photocatalytic treatment of organic pollutants. Raman analysis was carried out to study the vibrational characteristics of the samples. Further, the prepared nanocomposite was examined for its applicability in photocatalysis, by analysing its degradation ability on Eosin yellow and Eosin Blue dyes under white light LED irradiation. The composite exhibited significant degradation ability than the pure nanoparticles, which makes it an ideal candidate for the treatment of organic pollutants. The nanocomposite exhibited ferromagnetic behaviour as confirmed through Vibrating sample Magnetometry, so it can be easily retrieved after the treatment. The prepared ZrO2/Fe2O3 nanocomposite was tested for its antibacterial efficacy against two Gram positive bacteria (Enterococcus faecalis, Staphylococcus aureus) and two Gram negative bacteria (Escherichia coli, Pseudomonas aeruginosa). From the antibacterial studies it was validated that the nanocomposite exhibited significant antibacterial efficiencies against the bacteria. Hence the prepared nanocomposite has been proved to be a potential candidate for the treatment of organic pollutants as well as for antibacterial treatment.

Effects of yittria stabilised ZrO2 nanoparticles on the strengthening mechanisms in AlSi10Mg fabricated by LPBF

Effects of yittria stabilised ZrO2 nanoparticles on the strengthening mechanisms in AlSi10Mg fabricated by LPBF

Efficient photocatalytic degradation of Rhodamine B dye by undoped and zinc doped zirconium dioxide NPs

Undoped and Zinc-doped Zirconium Dioxide (ZrO2) nanoparticles (NPs) were synthesized via the co-precipitation method, employing Zirconium (IV) Oxynitrate hydrate (ZrO2N2·xH2O), Zinc Sulfate (ZnSO4·7H2O), and ammonia solution as precursor materials at room temperature. A comprehensive characterization of the structural, morphological, optical, and catalytic properties of the prepared samples was conducted using various techniques. Powder X-ray diffraction (PXRD) analysis revealed that the synthesized NPs exhibited a tetragonal phase structure, with crystallite sizes decreasing as doping concentration increased. Scanning electron microscopy (SEM) images confirmed the spherical shape of the NPs. Energy-dispersive X-ray spectroscopy (EDX) verified the presence of Zr, O, and Zn elements with high purity. Raman spectroscopy corroborated the tetragonal structure of the synthesized ZrO2 NPs. Ultraviolet–visible (UV–Vis) spectroscopy studies determined the cutoff wavelengths, while Tauc plot enabled the calculation of band gap energies. Fourier transform infrared spectroscopy (FTIR) confirmed the functional groups present in the synthesized samples. Photoluminescence spectroscopy provided evidence of defects and charge carrier recombination processes. The catalytic efficacy of the synthesized ZrO2 NPs was demonstrated through the degradation of Rhodamine B dye under visible and UV light.

Synthesis and characterizations of nanohybrids based on amino silane-graphene oxide decorated by zirconium oxide nanoparticles

This study aims to synthesize graphene oxide using the modified Hummers method and subsequently functionalize the surface of graphene oxide with amino silane N-(b-aminoethyl)-c-aminopropyltrimethoxysilane (AEAPTMS), resulting in silane-graphene oxide (SGO). The surface of SGO is then decorated with zirconium oxide (ZrO2) nanoparticles, generating SGO-ZrO2 nanohybrids. All the synthetized materials GO, SGO and SGO-ZrO2 were subjected to various characterization techniques, including Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Thermogravimetric analysis (TGA), Zeta potential measurement and Scanning electron microscope (SEM). The results revealed that GO nanosheets were decorated with ZrO2 nanoparticles through covalent bonding with AEAPTMS.

Microenvironment-Responsive Hydrogel Enclosed with Bioactive Nanoparticle for Synergistic Postoperative Adhesion Prevention.

Postoperative adhesion (PA) is a severe complication of abdominal surgery caused by the inability of clinical physical barriers to cope with diverse pathological factors in the process of PA formation. Herein, we described a multifunctional hydrogel composed of bioactive nanoparticles (BNs) and dual-responsive hydrogel to serve as a combination of physical and pharmacological therapy for preventing PA. Specifically, BNs with pro-inflammatory cell-targeted aggregation were designed by integrating hyaluronic acid onto the polydopamine (PDA)-coated hollow ZrO2 nanoparticles loaded with antimicrobial peptides and platelet lysates that can eliminate bacterial infection and promote tissue repair. PDA can remove the excessive reactive oxygen species (ROS) and thus suppress the oxidative stress damage and accompanying inflammation in the presence of high ROS. The dynamically cross-linked host hydrogel presents injectable yet microenvironment-responsive properties, which enables complete coverage of the uneven tissue and instantly forms a physical barrier to effectively isolate injured tissues and neighboring organs, and synchronously acts as a niche to deliver the BNs in a controlled way. The hydrogel demonstrates a remarkable antiadhesion effect in a rat cecum-abdominal wall adhesion model. Together, this "all-in-one" composite hydrogel strategy capable of a physical barrier capability and pharmacological effects represents a promising clinical solution to prevent PA.

Enhancing wind turbine blade protection: Solid particle erosion resistant ceramic oxides-reinforced epoxy coatings

In recent days, it is crucial for the globe to shift fossil fuel energies to renewable energies such as hydroelectric, wind, solar, tidal, geothermal, etc. to mitigate global warming issues. Wind energy has been regarded as one of the renewable energy sources to rely on in the future. In this aspect, wind turbine blade maintenance is quite a challenge in tropical areas like India. One of the main reasons why wind turbine blades get damaged and produce less energy is solid particle erosion. In the present work, epoxy nanocomposite coatings reinforced with Al2O3, ZrO2, and CeO2 nanoparticle fillers have been applied on glass fiber reinforced polymer (GFRP) substrates using a simple spray coating method. These nanoparticles have been prepared in-house by solution combustion synthesis (SCS) route using urea, glycine, and oxalyl dihydrazide fuels, respectively. X-ray diffraction, field emission scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy have been used to characterize the materials and coatings. Epoxy coatings with different Al2O3, ZrO2, and CeO2 nanoparticle concentrations have been subjected to solid particle erosion resistance tests at impinging angles of 30°, 60°, and 90°. ZrO2 and CeO2 nanoparticle-reinforced epoxy coatings show much better resistance to solid particle erosion than Al2O3-reinforced coatings. Estimated average erosion rates are 17 and 11.3 × 10−3 mm3 g−1, respectively, for epoxy coatings with 20 and 40 wt% ZrO2 nanoparticles. However, GFRP substrate and neat epoxy (EP) coating show much higher erosion rates with respect to nanoparticles-reinforced epoxy coatings. To ascertain a correlation between H3/E2 and the solid particle erosion rates of the coatings, nanoindentation tests have been carried out. Tensile strength and initial modulus of all the coatings are found to be directly proportional to the average erosion rates, whereas, elongation at break shows an inverse relationship with the average erosion rate. This correlation of mechanical properties with solid particle erosion performance can play a critical role in the development of realistic simulation of protective coatings for wind turbine blades.