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Magnesium aluminate, MgAl2O4, and other alumina-based spinels are refractory ceramics with high hardness and resistance to chemical attack while also being possible microwave dielectrics. Pure MgAl2O4 can be optically transparent when fully dense. Spinels exhibit inversion, which results in disorder among occupancy of A and B site cations. The goal of this study was to examine the effects of mechanical activation and composition on the temperature required for spinel formation and the site occupancy in the resulting spinel. MgAl2O4 was produced by solid state reaction between MgO and alpha-Al2O3. The starting powders were mixed by ball milling to homogenize the powders without significant particle size reduction. Mechanical activation of mixed powders was performed in a high-energy planetary ball mill in air for 1 h. Powders were compacted at 300 MPa. Heat treatments were performed in air, at temperatures ranging from 1200 to 1500 °C with 2 h dwell time, to determine the amount of spinel formation as a function of temperature. Phase composition and microstructure of initial powders and heated samples were determined by means of X-ray diffraction, particle size analysis, and scanning electron microscopy. The influence of milling and consolidation parameters were studied by electrical measurements and mechanical characterization. The main results of this study were that mechanical activation for 60 minutes initiated a mechano-chemical reaction, and resulted in spinel formation at much lower temperatures than within non-activated powders. Microstructures of ceramics sintered below 1400 oC indicated that final stage sintering started at much lower temperatures for activated samples than for non-activated samples. Changes in microstructure parameters, as a consequence of mechanical treatment and subsequent heating of investigated powder mixtures, strongly affect electrical and mechanical properties of the final ceramics.

Single crystalline phase MgAl2O4 is made from the predetermined composition of MgO-Al2O3 powder mixture by using ball-milling. Mixtures of MgO and Al2O3 are treated in planetary ball mill for 30, 60, 90 and 120 minutes, in air. The aim of this experiment was to examine phase composition, microstructure, and densification behavior of all sintered samples and to find out which sample has the best features for further use. After sintering in dilatometer at 1500 °C, XRD patterns and SEM images were recorded. The results show that mechanical activation is an efficient method to improve the densification behavior of MgAl2O4 sintered specimens. With the prolonged milling time, densities increased, reaching the maximum value of 2.8 g/cm3 for sample activated 120 minutes.

The peculiarities of sinter-crystallization of La2O3 center dot SrO center dot 5B(2)O(3) fine glass powder (below 1 mu m) are investigated and discussed. The sintering was studied by contactless optical dilatometry and porosity measurements. The crystallization process was evaluated by differential scanning calorimetry (DSC) and the crystalline phase formation was analyzed by X-ray diffraction (XRD). Finally the microstructures of the samples sintered at different temperatures were observed by field emission scanning electron microscope (FESEM). The specific aim of this study was to highlight the influence of sintering temperature and heating rate on the densification process and the final structure of glass-ceramic samples. It was shown that zero water adsorption and minimum closed porosity of similar to 3% were obtained at heating rate of 2 degrees C/min and at about 1 h holding at 690 degrees C. The temperature increase accelerated intense foaming process that resulted in formation of total porosity of 35-45%. It was also demonstrated that the foaming depended on the heating rate: the higher the heating rate - the more intensive was the bloating. The observed foaming process was related to intensive crystallization and re-crystallization of La2O3 center dot SrO center dot 5B(2)O(3) crystal phase. The phase formation processes entirely completed after 30-60 min at 730-740 degrees C with the formation of intriguing and unusual crystal structures.

Sintered alumina powder represents suitable material for usage in various industry fields (e.g., as chip carriers in electronics, microwaves, jewelry production), due to convenient physical properties, such as sinterability, electrical and mechanical features. Those properties can be modified by addition of different oxides and/or mechanical treatment. Therefore, in this investigation the alumina was doped with 1 wt. % of Cr2O3, Mn2O3 and NiO, respectively, followed by 1 hour of mechanical activation at 400 rpm in planetary ball mill. Sintering of powder mixtures was tracked by sensitive dilatometer up to 1400 °C. The final density values varied from cca. 2 ̶ 3.2 g/cm3. Changes in microstructure were observed by means of SEM. The influence of additives along with mechanical activation is monitored trough changes in electrical permittivity and loss tangent. Compared to pure alumina, the additives lower the relative permittivity and increase dielectric losses. For a given mixture, the sintering increases the relative permittivity and decreases losses.

Recently, with the huge use of smart gadgets, developing of smart jewelry represents a very interesting segment in material science, as well as in electronic science. Alumina is widely used ceramic in many industrial fields as pigments, catalysis, microelectronics, etc., mostly because of its low cost and appropriate mechanical and electrical properties, high surface area and thermal stability. Also, modified alumina could be applied in production of smart jewelry. Thus, the main objectives of this investigation is to improve features of sintered alumina doped with Mn2O3 along with mechanical treatment, in order to obtain strong ceramic with low values of dielectric loss and low relative dielectric permittivity, as well as esthetic. Commercial alumina powder was doped with 1 wt % of manganese oxide and treated in planetary ball mill for an hour. Characteristic temperatures of both powders (non-activated and activated one) were investigated in detail by DTA and TG analyses. After sintering at 1200, 1300, and 1400 oC for 2 h, XRD patterns and SEM images were recorded. Furthermore, mechanical and electrical properties were examined for all sintered samples.