Alumina-zirconia (Al2O3-ZrO2) composite ceramics were prepared by means of cross spraying and hydrothermal method under atmospheric pressure with nanometer powders doped with ZrO2 as the raw material. Then, the prepared powders and ceramics were characterized by SEM, XRD and BET methods. The results showed that combining cross spraying with hydrothermal method under atmospheric pressure could improve the dispersity of the ZrO2 composite ceramics nanopowders, while adding Al2O3 accelerated the low temperature sintering for 3Y-ZrO2 and improved the bending strength, fracture toughness and density of ZrO2 composite ceramics. In addition, through optimization the bending strength and fracture toughnessof the obtained ceramic, were 1,150 MPa and 8.2 MPa∙m1/2 respectively.
Micropowder MgCO3 was added into magnesite as raw materials to prepare magnesia using a two-step calcination method. The sample magnesite was characterized use X-ray diffraction (XRD) and scanning electron microscopy (SEM). Experimental results showed that the sample insulated at 1600° C for 3 hours before and after sintering presented a linear change rate of 15.6 % in the case of without adding micropowder MgCO3, the prepared magnesia had a bulk density of 2.31 g/cm3 and apparent porosity of 32.8 %, while MgO grain size was 3.11 μm. In the case of adding 8 % micropowder MgCO3, the sample magnesite before and after sintering showed a linear change rate of 17.9 %. The bulk density, apparent porosity of prepared magnesia were 2.46 g/cm3 and 28.1 % respectively, while the grain size of MgO was 5.15 mm.
The method of anti-hydrated of CaO-MgO was investigated in this paper. Take the magnesium calcium granulated substance as raw material, through studied material granularity, weight and other factors to influence anti-hydration of magnesium calcium. It is discovered that granularity of material influence on the anti-hydration of CaO-MgO, and confirm that this method is reliability and validity.
The bioactive glasses 58S was first prepared using sol-gel technique and the 45S5 bioactive glass was prepared through melting method. The above bioactive glasses were then grounded into fine powders, and each of the glass powders and their mixtures was doped with the porogen in certain ratios respectively. The bioactive porous materials were finally produced through sintering. We investigated the microstructure, surface morphologies, bending strength and bioactivity of the porous materials via in vitro method combined with DTA, SEM and FTIR techniques. The results show that the porous material made from the 58S and 45S5 mixture possesses the best bioactivity and bio-mineralization function among all samples, thus is a very promising bioactive material for bone defects filling or bone tissue engineering scaffolds.
The influence of the light burning temperature on the sintering property of nature dolomite has been investigated by two-step sintering process in the temperature range 1500 °C to 1600 °C. The resulting bulk densities and apparent porosities of the sintered dolomite samples were examined, and analyzing the sintered dolomite by scanning electron microscopy and X-ray diffraction were performed. The results showed light burned at 850 °C for 3 h, the main phases of the dolomite with 3-5 grain size were MgO, CaO and little CaCO3, and then fired at 1600 °C,the density of sintering dolomite reached to 3.38 g/cm3, the apparent property was 1.2 %, the size of MgO grain up to 3.75 μm . However when dolomite light burned at 1050 °C for 3 h, the main phases were MgO and CaO, and then fired at 1600 °C,the density of sintering dolomite only was 3.30 g/cm3, the apparent property was 2.3 %, the size of MgO only was 3.05 μm .
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