Method for preparing super high temperature zirconia ceramic fiber
A zirconia ceramic and ultra-high temperature technology, applied in the field of heat preservation and refractory materials, can solve the problems of multi-process, complex and high fiber cost of raw materials, and achieve the effect of simple synthesis process, stable high-temperature performance and single composition
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Embodiment 1
[0029] The preparation method of the fully stable cubic phase zirconia crystal fiber of the present invention adopts the following steps:
[0030] (1) Weighing 40.85g of yttrium nitrate and 100g of zirconium carbonate according to the ratio of yttrium oxide: zirconia molar ratio=10%: 90% and dissolving them in deionized water. 2 times 329.2g; according to the molar ratio of zirconium carbonate: nitric acid = 1:4, measure 183ml of nitric acid (content 65%-68%), and add nitric acid to the mixture of zirconium carbonate and yttrium nitrate at room temperature 30°C under stirring conditions In the solution, continue to stir for 2 hours after the addition to obtain a colorless and transparent reaction solution, which is a composite polymerization solution containing yttrium and zirconium ions.
[0031] (2) The viscosity of the yttrium-zirconium composite sol spinning solution obtained by concentrating under reduced pressure is within the scope of 2~10Pa s;
[0032] (3) Spinning by...
Embodiment 2
[0036] As described in Example 1, the difference is that in the step (1), the consumption of deionized water is changed to 4 times by 2 times of the total mass of yttrium nitrate and zirconium carbonate, that is, changed from 329.2g to 658.4g; zirconium carbonate; The molar ratio of nitric acid is changed from 1:4 to 1:4.5, the amount of nitric acid is changed from 183ml to 206ml, and the concentration of the spinning solution concentrated under reduced pressure in step (2) is changed from 2-10 Pa·s to 10-15Pa·s.
Embodiment 3
[0038] As described in Example 1, the difference is that the consumption of deionized water in step (1) should be 5 times by 2 times of the total mass of yttrium nitrate and zirconium carbonate, that is, change 823g from 329.2g; zirconium carbonate: nitric acid The molar ratio is changed from 1:4 to 1:5, the amount of nitric acid is changed from 183ml to 229ml, and the concentration of the spinning solution concentrated under reduced pressure in step (2) is changed from 2-10 Pa·s to 20-25Pa·s.
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