A method for burning, synthesizing, and casting y3al5o12 ceramics
A technology of y3al5o12 and combustion synthesis, which is applied in the field of combustion synthesis and casting of Y3Al5O12 ceramics, which can solve the problems of sintering cycle and easy generation of impurities for materials with large sizes that are difficult to shape, and achieve the effects of rapid synthesis, low reaction pressure and high efficiency
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specific Embodiment approach 1
[0018] Specific implementation mode 1: a kind of Y in this implementation mode 3 al 5 o 12 The method for the combustion synthesis melting and casting of ceramics is carried out in the following steps:
[0019] 1. Put the nitrate in a drying oven to dry separately to obtain a nitrate reactant;
[0020] Two, the metal powder is placed in a vacuum drying oven for drying treatment to obtain a metal powder reactant; wherein the metal powder reactant is a mixture of Al and Ti, and the molar ratio of Al and Ti is 5:3;
[0021] 3. The diluent is dried in a vacuum drying oven to obtain the diluent; wherein the diluent is made of Al 2 o 3 and Y 2 o 3 Composition, and Al in the system after reaction 2 o 3 and Y 2 o 3 The molar ratio is 5:3;
[0022] 4. Mix the nitrate reactant obtained in step 1, the metal powder reactant obtained in step 2, and the diluent obtained in step 3 by ball milling, then put them into the reaction device, ignite the raw materials, and carry out the ...
specific Embodiment approach 2
[0028] Specific embodiment two: the difference between this embodiment and specific embodiment one is: the nitrate reactant described in step one is Y(NO 3 ) 3 and Al(NO 3 ) 3 one or a mixture of the two. Other steps and parameters are the same as those in Embodiment 1.
[0029] When the nitrate reactant in the present embodiment is a mixture, both are mixed in an arbitrary ratio.
specific Embodiment approach 3
[0030] Embodiment 3: This embodiment differs from Embodiment 1 to Embodiment 2 in that the drying treatment described in step 1 is achieved by drying at a temperature of 70-90° C. for 8 hours to 12 hours. Other steps and parameters are the same as one of the specific implementation modes 1 to 2.
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Abstract
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