Reactions responsible for mass loss during pressure less sintering of Si3N4 ceramics with LiYO2 additive

The reactions were investigated with emphasis on the mass loss during pressureless sintering of Si3N4 ceramics without powder bad. A Si3N4 powder compacts with LiYO2 additive were heat-treated at different temperatures under the pressure of N2 of 0.1 MPa.. The mass loss increased with increasing temperature as well as with increasing additive content. It is expected that the major mass loss should be caused by volatilisation of lithia due to its high vapour pressure. However, the results of the chemical analysis of the samples are in contradiction with this assumption.Physical chemistry 2004 : 7th international conference on fundamental and applied aspects of physical chemistry; Belgrade (Serbia); 21-23 September 200

Kinetics of the alpha-beta Phase Transformation in Seeded Si3N4 Ceramics

The alpha-beta phase transformation in Si3N4 was studied for seeded samples using all Y2O3-Al2O3 mixture as a sintering aid. The concentration of beta-seeds varied from 0 to 5 wt.%. The results showed that alpha-beta phase transformation followed the first-order reaction. The calculated activation energy for seeded samples was in the range from 348 to 3 78 KJ/mol, indicating boundary reaction as the rate limiting step

Synthesis and characterization of biomorphic CeO2 obtained by using egg shell membrane as template

A new technology based on bio-templating approach was proposed in this paper. Egg-shell membrane (ESM) has been employed as a natural biotemplate. Fibrous oxide ceramics was prepared by wet impregnation of biological template with water solution of cerium nitrate. The template was derived from membranes of fresh chicken eggs. Repeated impregnation, pyrolysis and final calcination in the range of 600 to 1200 °C in air resulted in template burnout and consolidation of the oxide layers. At low temperatures, the obtained products had structure which corresponded to the negative replication of biological templates. Unique bio-morphic CeO2 microstructures with interwoven networks were synthesized and characterized by scanning electron microscope (SEM) and X-ray diffraction (XRD), whereas low-temperature nitrogen adsorption (BET) method was used in order to characterize porous properties

Effect of Milling Time on Mechanical Properties of Anorthite Obtained by Thermal Transformation of Ca-LTA Zeolite

Anorthite ceramics was fabricated from calcium exchanged Na-LTA zeolite. The powder compacts of Ca-LTA zeolite were sintered at different temperatures ranging between 1100 and 1400°C. It was found that the temperature of 1100°C was sufficiently high to trigger formation of anorthite which stayed stable even at temperature as high as 1400°C. The highest relative density and the lowest open porosity were measured in samples sintered at 1200°C for 3 h. The effect of milling time of Ca-LTA zeolite precursor on density, microstructure and mechanical properties of samples sintered at 1200°C for 3 h was investigated. The particle size refinement appeared to be beneficial in accelerating densification process and improving mechanical properties. The density, compressive strength and hardness of anorthite ceramics obtained from non-milled precursor were measured to be 70.5 %TD, 64 MPa and 1.45 GPa, respectively. On the other side the anorthite ceramics obtained from 24-hour-long milled zeolite precursor had density of 83.9 %TD, compressive strength of 101 MPa and hardness of 3.44 GPa

Permanent disposal of Cs ions in the form of dense pollucite ceramics having low thermal expansion coefficient

A promising method for removal of Cs ions from water and their incorporation into stable crystal structure ready for safe and permanent disposal was described. Cs-exchanged X zeolite was hot-pressed at temperature ranging from 800 to 950 °C to fabricate dense pollucite ceramics. It was found that the application of external pressure reduced the pollucite formation temperature. The effect of sintering temperature on density, phase composition and mechanical properties was investigated. The highest density of 92.5 %TD and the highest compressive strength of 79 MPa were measured in pollucite hot-pressed at 950 °C for 3 h. Heterogeneity of samples obtained at 950 °C was determined using scanning electron microscopy. The pollucite hot-pressed at 950 °C had low linear thermal expansion coefficient of ∼4.67 × 10−6 K−1 in the temperature range from 100 to 1000 °C. © 201

Novel basalt-stainless steel composite materials with improved fracture toughness

This paper presents the technological process for obtaining basalt-stainless steel composite materials and testing their physical and mechanical properties. The phases of the technological process consist of: milling, homogenization, pressing, and sintering to obtain composite materials with improved fracture toughness. Andesite basalt from the deposit site "Donje Jarinje", Serbia, was used as a matrix in the composites, while commercial austenitic stainless steel 316L in the amount of 0-30 wt.% was used as a reinforcement. Although the increase of 316L amount caused a continuous decrease in the relative density of sintered samples, the relative density of sample containing 30 wt.% of 316L was above 94%. The 316L grains, which possess a larger coefficient of thermal expansion than the basalt matrix, shrinking faster during cooling from sintering temperature resulting in the formation of compressive residual stress in the basalt matrix surrounding the spherical steel grains. The presence of this stress activated toughening mechanisms such as crack deflection and toughening due to compressive residual stress. The addition of 20 wt.% of reinforcing 316L particles increased the fracture toughness of basalt by more than 30%. The relative density of these samples was measured to be 97%, whereas macrohardness was found to be 6.2 GPa

Synthesis and characterization of luminescent Pr3+–doped hydroxyapatite nanopowder as a potential biomaterial for bioimaging applications

Praseodymium doped calcium hydroxyapatite (PrHAP) nanopowder was synthesized by the co-precipitation method and characterized by X-Ray Diffraction, Fourier Transform Infrared, and Fluorescence Spectroscopy. Characterization studies from XRD and FTIR spectra showed that obtained crystals are monophase hydroxyapatites and that the sample particles are of nano size. A fluorescence study has shown that PrHAP particles have fluorescent emission under UV‐ Visible excitation. These results may open new avenues for developing bioactive materials for bone regeneration and fluorescent probes for bio-imaging applications

Synthesis and characterization of luminescent Pr3+ –doped hydroxyapatite nanopowder as a potential biomaterial for bioimaging applications

Praseodymium doped calcium hydroxyapatite (PrHAP) nanopowder was synthesized by the co-precipitation method and characterized by X-Ray Diffraction, Fourier Transform Infrared, and Fluorescence Spectroscopy. Characterization studies from XRD and FTIR spectra showed that obtained crystals are monophase hydroxyapatites and that the sample particles are of nano size. A fluorescence study has shown that PrHAP particles have fluorescent emission under UV‐ Visible excitation. These results may open new avenues for developing bioactive materials for bone regeneration and fluorescent probes for bio-imaging application