59 research outputs found

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

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    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

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    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

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    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 Ā°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

    Fabrication of Porous Anorthite Ceramic Insulation Using Solid Wastes

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    Porous anorthite (CaAl2Si2O8) ceramics, suitable for thermal insulation in buildings, were obtained using waste seashells as a source of CaO, kaolin as a source of Al2O3 and SiO2 and banana peel as a pore former. Changing the volume of banana peel as well as the processing temperature was found to be an effective approach to control the thermo-mechanical properties of the obtained anorthite ceramics. The sintering of powder compacts containing up to 30 wt% banana peel at temperatures ranging from 1100 to 1200 Ā°C resulted in anorthite ceramics possessing up to 45% open porosity, a compressive strength between 13 and 92 MPa, a bulk density between 1.87 and 2.62 g/cm3 and thermal conductivity between 0.097 and 3.5 W/mK. It was shown that waste materials such as seashells and banana peel can be used to obtain cost-effective thermal insulation in buildings

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

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    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 1400Ā°C. It was found that the temperature of 1100Ā°C was sufficiently high to trigger formation of anorthite which stayed stable even at temperature as high as 1400Ā°C. The highest relative density and the lowest open porosity were measured in samples sintered at 1200Ā°C for 3 h. The effect of milling time of Ca-LTA zeolite precursor on density, microstructure and mechanical properties of samples sintered at 1200Ā°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

    Physico-chemical and mechanical properties of geopolymer/zircon composites

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    The effect of zircon (ZrSiO4) on the physico-chemical and mechanical properties of geopolymer/zircon composites was examined in this study. Four geopolymer/zircon composites containing 10, 20, 30 and 40 wt.% zircon were prepared from metakaolin with alkali activators. Characterization of the obtained geopolymers was performed by X-ray diffraction (XRD), Scanning electron microscope (SEM-EDS), Fourier transform infrared spectroscopy (FTIR) and Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF). XRD results did not confirmed the formation of interconnected phases between added zircon, starting aluminum silicates and alkali activators. Compressive strength of prepared geopolymer was examined. The maximum obtained compressive strength of 70.15 MPa was measured in sample containing the smallest fraction of zircon, i.e., 10 wt.%. Addition of larger amount of zircon (20 wt.%) hinders the progress of geopolymerization reaction and consequently decreases compressive strength

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

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    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 Ā°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 Ā°C for 3 h. Heterogeneity of samples obtained at 950 Ā°C was determined using scanning electron microscopy. The pollucite hot-pressed at 950 Ā°C had low linear thermal expansion coefficient of āˆ¼4.67 Ɨ 10āˆ’6 Kāˆ’1 in the temperature range from 100 to 1000 Ā°C. Ā© 201

    High-density ceramics obtained by andesite basalt sintering

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    In the present study, andesite basalt originated from the deposit site ā€œDonje Jarinjeā€, Serbia, was examined as a potential raw material for high-density ceramics production. The production of high-density ceramics included dry milling, homogenization, cold isostatic pressing and sintering in the air. To determine the optimal processing parameters the sintering was conducted at 1040, 1050, 1060, 1070 and 1080Ā°C, and afterwards the sintering duration was varied from 30 to 240min at the optimal sintering temperature of 1060Ā°C. Characterization of the starting and sintered materials included the estimation of particle size distribution, density, hardness and fracture toughness complemented with X-ray diffraction, optical light microscopy, scanning electron microscopy and energy dispersive spectroscopy analysis. Phase transformations did not occur during processing in the investigated temperature range from 1040 to 1080Ā°C. The obtained research results showed that 99.5% of relative density and the highest hardness and fracture toughness values of 6.7GPa and 2.2MPaā€¢m1/2, respectively, were achieved for the andesite basalt sintered at 1060Ā°C for 60min in the air. The results of the present study confirmed that the sintered andesite basalt can be used as a high-density ceramic material for various industrial applications

    Novel basalt-stainless steel composite materials with improved fracture toughness

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    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
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