Ceramic Materials and Components for Energy and by Dongliang Jiang, Yuping Zeng, Mrityunjay Singh, Juergen

By Dongliang Jiang, Yuping Zeng, Mrityunjay Singh, Juergen Heinrich

This quantity of the Ceramic Transactions sequence compiles a couple of papers provided on the ninth overseas convention on Ceramic fabrics and elements for strength and Environmental purposes (9th CMCEE) in Shanghai, China and was once the continuation of a sequence of foreign meetings held around the world during the last 3 many years. This quantity includes chosen peer reviewed papers from greater than three hundred shows from around the world. The papers during this quantity additionally spotlight and emphasize the significance of synergy among complicated fabrics and part designs.

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Additional info for Ceramic Materials and Components for Energy and Environmental Applications: Ceramic Transactions Volume 210 (Ceramic Transactions Series)

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Figure 2. 5)03 ceramics with sintering temperatures of 1300°C ~1375°C are shown in figure 3. The porosity decreased with increasing sintering temperature and no pore was observed at temperatures of 1325°C, but non-uniformity grain were observed, and abnormal grain growth started to appear between the sintering temperatures of 1325°C and 1350°C, These may directly affect the microwave dielectric properties. Figure 3. 5)03 ceramics with sintering temperatures of 1300°C ~1375°C are shown in figure 4.

Prepared powders were dried and calcined at 1100°C for 2h in air. 5)03 with different sintering aids of 10 mol % B2O3, 10 mol % BÍ2O3, and 10 mol % V2O5 additions as sintering aids and re-milled for 12h. The fine powder together with the organic binder was pressed into pellets with dimensions of 11 mm in diameter and 5 mm in thickness was made by pressing at a pressure of 25kg/cm3. These pellets were sintered at temperatures of 1300°C ~ 1375°C for 6 h in air. The heating and cooling rates were both set at 5°C /min.

There is not much difference of covalent bond strength of Al-Al or Ti-Ti, but the covalent bond of Ti-C or Ti-Al in TÍ3AIC2 is obviously stronger than that in T12AIC, which is consistent with the result of experiment that the mechanics property of TÍ3AIC2 is better than that of T12AIC, and TÍ3AIC2 is easier synthesized than Ti2AlC[4]. 1403 face)c face)_A1 In the composite of T12 AIC/T1B2, Ti atoms on the interface connect to C, Al and B of two phases of T12AIC and T1B2. Therefore, the number of copies of Ti atom in TÍ2AIC/T1B2 is less than that in Ti2AlC or TiB2, and the net charge of Ti in Ti2AlC/TiB2 is higher than that in Ti2AlC or TiB2 (Table 1).

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