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Magnesia MgO

MgO is has cubic crystal structure, as shown in Fig. 2.10. MgO ceramics have excellent thermal and mechanical properties with a high melting point of 2850 °C and low density of 3.58 g cm. It has an isotropic cubic crystal strucmre, which meets one of the requirements to be transparent. PolycrystaUine infrared-transparent MgO is a potential substitute for sapphire IR windows and protectors for sensors. Due to the high sintering temperature required for full densification of MgO, fabrication of transparent MgO ceramics is stiU a challenge. Almost aU techniques discussed above have been used to prepare transparent MgO ceramics [3]. [Pg.46]

The addition of LiF as sintering aid could reduce the sintering temperature of MgO transparent ceramics [141, 142]. It has been acknowledged that densification [Pg.46]

MgO ceramics. The MgO green bodies were sintered at 1400 for 2 h in ambient atmosphere. The as-sintered MgO ceramics had a relative density of 98.1 % with an average grain size of 6 pm and an average hardness of 6.8 GPa [3]. [Pg.48]

4 Magnesia (MgO) - Magnesia is also a possible support material having a good thermal stability that can be used as washcoat material as well. Hashimoto et al. have described a preparation by vapour oxidation that can lead to a large surface area and ultra-fine single crystal MgO. It is very resistant to thermal treatment and has a surface area above 72 m g after calcination at 1500°C.  [Pg.191]

Magnesium oxide has been reported to be active in methane complete oxidation by Berg and Jaras. The activity was somewhat lower compared with a Ba-substituted hexa-aluminate. The difference between the two catalysts decreased after calcination to 1500 °C. [Pg.191]


Fig. 16.1. Ionic ceramics, (a) The rocksalt, or NoCl, structure, (b) Magnesia, MgO, has the rocksalt structure. It can be thought of as an f.c.c. packing with Mg ions in the octahedral holes. ( ) Cubic zirconia ZrOj an f.c.c. packing of Zr with O in the tetrahedral holes, (d) Alumina, AljOj a c.p.h. packing of oxygen with Al in two-thirds of the octahedral holes. Fig. 16.1. Ionic ceramics, (a) The rocksalt, or NoCl, structure, (b) Magnesia, MgO, has the rocksalt structure. It can be thought of as an f.c.c. packing with Mg ions in the octahedral holes. ( ) Cubic zirconia ZrOj an f.c.c. packing of Zr with O in the tetrahedral holes, (d) Alumina, AljOj a c.p.h. packing of oxygen with Al in two-thirds of the octahedral holes.
Magnesia, MgO, is an example (Fig. 16.1b). It is an engineering ceramic, used as a refractory in furnaces, and its structure is exactly the same as that of rocksalt the atoms pack to maximise the density, with the constraint that like ions are not nearest neighbours. [Pg.168]

Copper (Cu) and zinc (Zn), when mixed, form the alloy brass. Magnesia (MgO) and alumina (AljOj) when mixed in equal proportions form spinel. Iron (Fe) and carbon (C) mix to give carbon steel. [Pg.321]

The result of deviation from unit activity is illustrated by the reduction of magnesia (MgO) with silicon. According to data provided, AG° for... [Pg.257]

Bitartrate of Magnesia—MgO, HO, 0B H, 0W —when excess of acid is employed. Six-sided prisms solublo in fifty-two parts of cold water. [Pg.1054]

Mg-PSZ represents magnesia, MgO, partially stabilized zirconia, Zr02, ceramics. These ceramics are strong and tough structural materials. The main characteristics of Mg-PSZ ceramics are... [Pg.85]

The substrates used in this study were (0001) sapphire (A1203), (001) magnesia (MgO), and amorphous fused silica (Si02). All substrates were obtained with surface finish to 0.025 / m, and were cleaned with isopropylalcohol (IPA) prior to PA A or APS application. The surfaces and interfaces after peel test were characterized using X-ray photoelectron spectroscopy (XPS). The PMDA-ODA PAA was cast from NMP solution. Figure l shows the structure of the PAA and the thermally imidized PMDA-ODA polyimide. [Pg.412]

Magnesia (MgO), used as an insulator for electrical heating devices, has a face-centered cubic structure like that of NaCl. Draw one unit cell of the structure of MgO, and explain why MgO is more brittle than magnesium metal. [Pg.944]

The Bessemer process is relatively less expensive but does not produce a product of high quality. It is not possible to exercise control over the composition of the product because the conversion occurs so quickly. Furthermore, this process does not effect the removal of phosphorus. The phosphorus pentoxide that is formed during the blow is reduced to phosphorus upon addition of carbon and hence remains as an impurity in the final product. Provision for the removal of phosphorus may be made by the use of the so-called basic Bessemer process, which employs a converter lined with magnesia (MgO), but this practice entails other disadvantages. In the United States, the acid Bessemer process is used exclusively and accounts for about 15% of the steel produced in this country. Steel so produced is used largely as structural steel, as reinforcement for concrete, and in the tinplate industries. [Pg.569]

Chlorination of magnesia (MgO) or magnesite (MgC03) in the presence of carbon or carbon monoxide... [Pg.524]

The compounding ingredients for preparation of adhesion test specimens, magnesia (MgO), zinc oxide, Zalba Special (hindered phenol antioxidant from E. I. duPont de Nemours and Co.), and Bakelite-brand t-butylphenolic resin CK-1634 (Union Carbide Corp.) were used as... [Pg.577]

Magnesia Magnesia (MgO) is produced from seawater or brine. In one process, the chloride brine is sprayed into a reactor where hot gasses convert the MgClg solution to MgO and HCl. The hfeO is slurried... [Pg.36]


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