Preparation method of yttria-stabilized zirconia tetragonal nano powder with high specific surface area
A technology of stable zirconia and high specific surface area, which is applied in the direction of nanotechnology, nanotechnology, nanotechnology, etc. for materials and surface science, can solve the problems of difficult control conditions, high raw material costs, long production cycle, etc., and achieve reduction Lower sintering temperature, improved mechanical properties, and improved densification
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Embodiment 1
[0031] Weigh 3.1283 g ZrOCl 2 ·8H 2 O and 0.0339 gY 2 o 3 , add excess 1:1 nitric acid and heat to dissolve Y 2 o 3 , to form a clear solution of yttrium nitrate, the weighed ZrOCl 2 ·8H 2 O is completely dissolved in it to obtain the mixed salt solution of the metal contained in the target product, then add 1.7532 g NaCl and 1.6936 g glycine to the solution, heat to dissolve completely, then concentrate the mixed solution until it is viscous, and put it into the set temperature It is ignited in a chamber with a constant temperature of 600°C. After the combustion is completed, the product is taken out, washed, filtered, and dried to obtain a specific surface area of 151 m 2 g -1 of (Y 2 o 3 ) 0.015 (ZrO 2 ) 0.97 of white powder.
Embodiment 2
[0033] Weigh 3.1283 g ZrOCl 2 ·8H 2 O and 0.1149 g Y (NO 3 ) 3 ·6H 2 O, add excess 1:1 nitric acid and heat to dissolve Y 2 o 3 , to form a clear solution of yttrium nitrate, the weighed ZrOCl 2 ·8H 2 O is completely dissolved in it to obtain the mixed salt solution of the metal contained in the target product, then add 2.2365 g KCl and 1.6936 g glycine to the solution, heat and dissolve completely, then concentrate the mixed solution to a viscous state, and put it into the set temperature Ignite in a chamber with a constant temperature of 500°C. After the combustion is completed, take out the sample, wash, filter, and dry to obtain a specific surface area of 325 m 2 g -1 of (Y 2 o 3 ) 0.015 (ZrO 2 ) 0.97 of white powder.
Embodiment 3
[0035] Weigh 3.0315g ZrOCl 2 ·8H 2 O and 0.1236 gY 2 (CO 3 ) 3 ·3H 2 O, add excess 1:1 nitric acid and heat to dissolve Y 2 o 3 , to form a clear solution of yttrium nitrate, the weighed ZrOCl 2 ·8H 2 O is completely dissolved in it to obtain the mixed salt solution of the metal contained in the target product, then add 2.9820 g KCl and 1.0312 g urea to the solution, heat and dissolve completely, then concentrate the mixed solution until viscous, and put it into the set temperature Ignition is carried out in a chamber with a constant temperature of 500°C. After the combustion is completed, the sample is taken out, washed, filtered, and dried to obtain a specific surface area of 378 m 2 g -1 of (Y 2 o 3 ) 0.03 (ZrO 2 ) 0.94 of white powder.
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