Preparation method of selective adsorbent for magnetic cesium
A cesium selective, adsorbent technology, applied in the field of preparation of magnetic cesium selective adsorbent, can solve the problems of easy hydrolysis, water solubility, poor radiation stability, etc., achieve fewer steps, good radiation resistance, and easy industrialization The effect of production
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[0030] like figure 1 Shown, the preparation method of magnetic cesium selective adsorbent provided by the present invention comprises the steps:
[0031] (1) To Ni powder and K 4 Fe(CN) 6 ·3H 2 Deionized water was added to the O mixture so that the K 4 Fe(CN) 6 ·3H 2 O completely dissolved; Ni powder and K 4 Fe(CN) 6 ·3H 2 The mass ratio of O is 1:5~1:10, the preferred value is 1:7; the amount of deionized water added is K 4 Fe(CN) 6 ·3H 2 20 to 30 times the mass of O, preferably 26 times;
[0032](2) Place the obtained dissolved matter in a constant temperature water bath at 95±5°C, add HCl solution dropwise therein, and keep stirring for 20-40min; the concentration of the added HCl solution is 1.0~3.0mol / L, preferably 2.4mol / L; the mass ratio of added HCl to Ni is 2:1 to 4:1, preferably 3:1; the stirring speed is 600 to 850 rpm, and the preferred value is 750 rpm;
[0033] (3) statically aging the obtained reactant at room temperature for 20 to 40 minutes, unti...
Embodiment 1
[0054] Accurately weigh a certain amount of 0.1g Ni powder and 0.76g K 4 Fe(CN) 3 ·3H 2 O in a 50mL beaker, add 20mL deionized water to dissolve K 4 Fe(CN) 3 ·3H 2 O dissolves completely. Then, 2 mL of 2.4 mol / L HCl solution was slowly added dropwise in a water bath at 95±5°C, and the reaction was stirred continuously for 30 minutes at a stirring speed of 750 rpm, and then aged at room temperature for about 30 minutes. Then, the precipitate was washed continuously with deionized water until the washing liquid was clear and transparent, and the pH remained basically unchanged. Finally, the precipitate was dried at a constant temperature of 100°C for 20 h.
Embodiment 2
[0056] Accurately weigh a certain amount of 0.1g Ni powder and 0.5g K 4 Fe(CN) 3 ·3H 2 O in a 50mL beaker, add 15mL deionized water to dissolve K 4 Fe(CN) 3 ·3H 2 O dissolves completely. Then, 3.2mL of 1.0mol / L HCl solution was slowly added dropwise in a water bath at 95±5°C, and the reaction was stirred continuously for 20min at a stirring speed of 600rpm, and then left at room temperature for about 40min. Then, the precipitate was washed continuously with deionized water until the washing liquid was clear and transparent, and the pH remained basically unchanged. Finally, the precipitate was dried at a constant temperature of 90°C for 24 hours.
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