Hydrate D-cerous tartrate ferroelectric functional material and preparation method thereof
A technology of tartaric acid and electric function, which is applied in the field of hydrated D-cerium tartrate ferroelectric functional material and its preparation, to achieve the effect of easy industrialization, good ferroelectric characteristics, and less process
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Embodiment 1
[0020] Embodiment 1, take by weighing 1.0mmol cerium nitrate and dissolve in deionized water, stir and dissolve, be made into the cerium nitrate solution that concentration is 0.05~0.1mol / L stand-by, take by weighing 1.5mmol D-tartaric acid, be dissolved in deionized water, Stir to dissolve, add 3.0mmol sodium hydroxide to dissolve, and make a sodium tartrate solution with a concentration of 0.05-0.1mol / L. Under stirring, add the cerium nitrate solution into the sodium tartrate solution, and a white precipitate is formed. After continuing to stir for a period of time, the precipitation is complete, filtered, and the precipitate is washed with distilled water for 3 to 5 times, and then vacuum-dried to obtain white hydrated tartaric acid. Ce powder.
Embodiment 2
[0021] Embodiment 2 is substantially the same as Embodiment 1, except that the D-tartaric acid is 1.0mmol or 2.0mmol.
Embodiment 3
[0022] Example 3. Weigh 1.0 g of cerium oxide and 1.5 g of D-tartaric acid and dissolve them in 40 to 50 mL of ethanol solution with a volume concentration of 85 to 90%, then place them in a polytetrafluoroethylene-lined stainless steel reaction kettle, stir well After dissolving, add oxalic acid to adjust the pH of the solution to 0.3-0.5, seal the stainless steel reactor, and react for 2-5 days at a temperature of 120-200°C. After the reaction is completed, reduce the temperature by 2-5°C per hour. cooling to room temperature to obtain colorless flaky cerium tartrate hydrate crystals; grinding the cerium tartrate hydrate crystals into a powder passing through a 100-mesh sieve to obtain white cerium tartrate hydrate powder.
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