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Showing 10 results for Zirconia

M. Kasiri Asgarani, A. Saidi, M. H. Abbasi,
Volume 28, Issue 1 (6-2009)
Abstract

The effects of mechanochemical treatment of monoclinic zirconia in high energy planetary ball mill on its phase transformation were investigated. The mechanical treatment in ball mill reduces the grain size, increases microstrain, and causes phase transition to metastable nanostructured tetragonal and cubic phases. XRD and TEM results show considerable amounts of amorphous phase during ball milling. Surface area measurements by BET method over long milling times reveal that ZrO2 particles are agglomerated with an amorphous phase as a binder. The mechanical treatment increases the reactivity of zirconia in chlorine gas. Annealing of ball milled zirconia in the chlorine atmosphere produces oxygen vacancy in zirconia (ZrO2-x) and causes the amorphous phase to be crystallized and to change into cubic and tetragonal phases. The chlorine atmosphere increases the stability temperatures of cubic and tetragonal phases to 800°C and 1000°C, respectively. In this situation, the energy of grain boundary and oxygen vacancy play important roles in the stability of tetragonal and cubic phases.
S. Salehi, M. H. Fathi, K. Raeissi,
Volume 29, Issue 1 (6-2010)
Abstract

The addition of ZrO2 particles to the HA coating has received considerable attention because ZrO2 particles increase the bonding strength between HA coating and substrate. In this study, nanostructured hydroxyapatite (HA)/yttria stabilized zirconia (YSZ) coatings were prepared by a sol–gel method. It was found that at 950ºC, the dominant phases were HA and tetragonal (t)-zirconia in 3YSZ, cubic (c)-zirconia in 8 YSZ and t-c-Zirconia in 5YSZ phases with the small amounts of β-tricalcium phosphate (β-TCP) and CaZrO3. The crystallite size of the coating was about ~20-30 nm for tetragonal and cubic zirconia grain size and 40-80 nm for hydroxyapatite grain size. Crack-free and homogeneous HA/YSZ composite coatings were obtained with no observable defects. In vitro evaluation in 0.9% NaCl showed that Ca2+ dissolution rate of composite coatings was lower than that of pure HA coatings. The decrease in electrochemical performance of these coated samples in comparison with the uncoated type 316L St.St could be associated with chloride ion and water penetration into the coating, transport of ions through the coating, and the subsequent electrochemical reactions at the coating–metal interface.
N. Miadi, H. Sarpoolaky, H. Ghassai,
Volume 32, Issue 1 (6-2013)
Abstract

In this study, mullite– irconia composite samples were prepared by reaction sintering of alumina and zircon powder via gel casting process. Gel casting is a new ceramic forming technique. This process is based on the casting of slurry, containing ceramic powder, dispersant and premix monomer solution. To achieve stabilized, high solid loading (80 wt%) and castable slurry, the rheological properties of slurry were optimized. The monomers polymerized the slurry to form gelled specimens. After gelation, the specimens were unmolded, then dried out under controlled condition. Burning out and sintering of the specimens was carried out in the range of 1400-1700°C. Apparent porosity and bulk density of the sintered samples were measured by soaking in water. Crystalline phase evolution and microstructure were determined by XRD and SEM techniques. Results showed that the reaction sintering and mullite formation was completed at 1700°C due to very slow diffusion of Al3+ ions within amorphous silica formed at the decomposition of zircon. The sintered samples at this temperature also showed the lowest apparent porosity (≈ 4%) and the highest bulk density (≈3.40 gr/cm-3).
R. Jamshidi-Alashti, M. Borouni, B. Niroumand,
Volume 32, Issue 2 (12-2013)
Abstract

Application of ceramic reinforcements is one of the effective and well-known ways to refine the microstructure of brittle metals such as magnesium. In this research, the influence of nano/micro particles of zirconia on the microstructure of cast AZ91 alloy was studied. At the first stage, nano and micro ZrO2 powders were blended through mechanical alloying procedure. In five specimens, the total amount of nano and micro reinforcements in the final mixture was fixed at 5 wt%, whereas their ratio was varied. Two other composites were also produced using 5wt% of nano or micro particles of zirconia. These powder mixtures were then stirred in the molten AZ91 at 650C by vortex method and finally cast in a sand mold at 615C. For comparison, two monolithic castings including a conventionally cast specimen and a super heat-treated sample were also cast. The average grain sizes for all composites were decreased with respect to both monolithic castings. The best results in terms of grain size and microstructure improvement were obtained for AZ91/5wt% nano ZrO2 composite with remarkable improvement in comparison with monolithic castings.
N. Setoudeh,
Volume 32, Issue 2 (12-2013)
Abstract

A powder mixtures of 18.72% wt, 17.67% wt Al2O3 and 63.6% wt zircon were prepared and milled in a planetary ball milled for one up to 10 hours in presence of air. After removal Iron impurity from as-milled samples, they were isothermally heated in temperature range of 1300-1450 0C for one hour in an air atmosphere. After cooling the samples, they were studied using XRD analyses. The XRD and PSA analyses were showed that the size of particles in the mixtures decreased with increasing of milling time and the mixtures became amorphous nature. The isothermal runs observed that pre-milling on the mixtures has great effect, wherever the zircon decomposition temperature and mullite formation temperature decreased to about 1300 0C in a one-hour-milled sample. The amount of tetragonal zirconia increased with increasing in milling time at 1300 0C, however the amount of tetragonal zirconia decreased with increasing of temperature up to 1450 0C. The amount of tetragonal zirconia at 1300 0C in the three hours milled samples was the highest value among all samples.
M. Rahmani, K. Janghorban , S. Otroj,
Volume 33, Issue 1 (7-2014)
Abstract

In this study, the effect of different amounts of Y2O3 on the properties of mullite-zirconia composites was investigated. For this purpose, these composites were fabricated by reaction-sintering of alumina and zircon as raw materials. Besides, the slip casting method was used for forming these composites, and sintering process was carried out at 1600 °C. Then, the physical and mechanical properties, phase composition and the microstructure of these composites were investigated. The results showed that yittria addition up to 0.5 wt.% has no effect on the properties of these composites. Besides, addition of more than 0.5 wt.% yittria formed solid solution with zirconia grains and led to stabilization of tetragonal zirconia phase and increasing of its amount. Hence, yittria addition increases the hardness and bending strength of composite by stabilizing tetragonal zirconia phase and then, decreasing the micro-crack formation during zirconia phase transformation. As results show, addition of 0.75 wt.% yittria leads to a considerable increase in the bending strength.
M. Rahmani, K.janghorban, S. Otroj,
Volume 33, Issue 2 (3-2015)
Abstract

In this study, the effect of different amounts of Y2O3 on the properties of mullite-zirconia composites was investigated. For this purpose, these composites were fabricated by reaction-sintering of alumina and zircon as raw materials. Besides, the slip casting method was used for forming these composites, and sintering process was carried out at 1600 °C. Then, the physical and mechanical properties, phase composition and the microstructure of these composites were investigated. The results showed that yittria addition up to 0.5 wt.% has no effect on the properties of these composites. Besides, addition of more than 0.5 wt.% yittria formed solid solution with zirconia grains and led to stabilization of tetragonal zirconia phase and increasing of its amount. Hence, yittria addition increases the hardness and bending strength of composite by stabilizing tetragonal zirconia phase and then, decreasing the micro-crack formation during zirconia phase transformation. As results show, addition of 0.75 wt.% yittria leads to a considerable increase in the bending strength
F. Shahriari Nogorani, M. Afari, M. A. Taghipoor, A. Atefi,
Volume 39, Issue 1 (5-2020)
Abstract

Practical applications of thermal barrier coatings with aluminide bond-coats are limited due to oxide scale spallation of the aluminide coating under applied thermal stresses. Considering the positive effects of oxygen-active elements or their oxides on the high temperature oxidation behavior, in this research zirconia was introduced into an aluminide coating. For this purpose, a Watts type bath was used to electroplate a layer of Ni-ZrO2 composite on a Ni-based substrate. Aluminizing was performed using the conventional two-step process at 760 and 1080 °C. Microstructural characterization of coatings in the as-coated conditions and after cyclic oxidation via 5-hour cycles at 1050 °C was performed using electron microscopy, energy dispersive spectroscopy and X-ray diffractometry. The results showed that the general three-zone microstructure of the simple high activity aluminide coatings develops below the pre-deposited nickel-zirconia layer and latter converts to a nearly un-alloyed porous NiAl. In spite of its porous surface layer, the zirconia modified coating has a higher oxidation resistance than the unmodified aluminide coating.

M. Farhadian, K. Raeissi, M. A. Golozar,
Volume 39, Issue 2 (8-2020)
Abstract

This work is focused on the effect of amorphous SiO2 addition on the phase transformation and microstructural evolution of ZrO2 particles. Considering the structural similarities between the amorphous ZrO2 and its tetragonal structure, XRD results showed initial nucleation of metastable tetragonal ZrO2 from its amorphous matrix upon heat treatment. This metastable phase is unstable in pure ZrO2 sample and transforms to a stable monoclinic phase at around 600 oC. However, addition of amorphous SiO2 to ZrO2 structure causes metastable tetragonal phase to remain stable up to around 1100 oC. The temperature range for stability of metastable tetragonal ZrO2 structure increased from about 150 oC in pure ZrO2 particles to around 500 oC in ZrO2-10 mol.% SiO2 composite powders. A further increase in SiO2 content up to 30 mol.% did not change the stabilization temperature range but the average particle size reduced around 1.6 times compared to pure ZrO2 particles. Stabilization of metastable tetragonal ZrO2 explained by constrained effect of SiO2 layer surrounding zirconia nuclei. The thickness of this SiO2 layer enhanced by increasing SiO2 content which limited the growth of ZrO2 nuclei resulting in finer particle sizes.

H. R. Karimi, H. Mansouri, M. R. Loghman Estarki, M. Tavoosi , H. Jamali,
Volume 40, Issue 1 (5-2021)
Abstract

This study aimed to compare the phase changes and morphology of yttria-stabilized zirconium oxide powders (YSZ) synthesized by co-precipitation and molten salt methods. Ammonia precipitating agent was used for the synthesis of YSZ powder by co-precipitation method and a mixture of sodium carbonate and potassium carbonate salts was used as a molten salt in the molten salt method. Samples were characterized by X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared Spectroscopy (FTIR), Thermal Gravimetric Analysis (TGA), and Differential Scanning Calorimetry (DSC) analysis. The results showed that only the sample prepared with zirconium oxychloride and yttrium nitrate by co-precipitation method had a single phase of yttria-stabilized zirconium oxide with tetragonal crystal lattice and particle size distribution in the range of 30 to 55 nm. The powder synthesized by the molten salt method contained a mixture of zirconia with monoclinic crystal lattice and yttria stabilized zirconia with tetragonal crystal lattice and particle size of 200 nm.


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