Extraction agent and adsorbent containing effective functional groups and application of extraction agent and adsorbent containing effective functional groups in extraction purification of thorium metal
A technology of extractant and adsorbent, which is applied in the field of extraction and separation of radioactive elements, and can solve the problems that cannot be completely removed
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[0071] The present invention also provides the preparation method of above-mentioned extractant, according to the type difference of extractant, the preparation method of described extractant is as follows:
[0072] In a preferred embodiment of the present invention, the extractant (E1 ) and (E 2 ) preparation method comprises the steps:
[0073] Compound shown in formula (IV) and R 1 R 2 NH is a raw material, and at a certain temperature, reacts to prepare an extractant (E 1 ) or (E 2 );
[0074]
[0075] Among them, X 1 , R 1 , R 2 is defined as above.
[0076] In a preferred embodiment of the present invention, the extractant (E 1 ) and (E 2 ) preparation method specifically comprises the steps:
[0077] 1) compound shown in formula (IV) and R respectively 1 R 2 NH is dissolved in an organic solvent, where, X 1 , R 1 , R 2 as defined above;
[0078] 2) The above two solutions are mixed and reacted to prepare the extractant (E 1 ) or (E 2 ).
[0079] W...
Embodiment 1
[0162] Embodiment 1 extractant (E 1-1 ) Synthesis of -1
[0163] Weigh 1.52g (13.1mmol) diglycolic anhydride and 2.87g (11.9mmol) R 1 R 2 NH(R 1 , R 2 selected from isooctyl), which were dissolved in 20mL of dichloromethane organic solvent respectively; the two solutions were mixed and reacted at 25°C; during the reaction, the mixed solution gradually became clear, and when it was completely clear, the reaction Complete (about reaction 12h), make extraction agent shown in formula (I) (wherein, X 1 for -O-, R 1 and R 2 The same is isooctyl); the prepared extractant is washed with high-purity deionized water to remove impurities, and then magnesium sulfate is added to the washed product to filter to obtain a water-free product, and the processed product is rotated The organic solvent was removed by evaporating and condensing apparatus, and then dried in a vacuum oven at 75°C for 12 hours, so as to obtain a high-purity extractant. Wash the prepared extractant several time...
Embodiment 2
[0165] Embodiment 2 extractant (E 1-2 ) Synthesis of -2
[0166] Weigh 3.78g (28.2mmol) of diglycolic acid and dissolve in 20ml of acetic anhydride, heat to 140°C on a magnetic heating stirrer and stir to reflux. During the reaction, the solid gradually dissolves and the solution gradually becomes clear, and stops after 4 hours For the reaction, excess acetic anhydride and acetic acid formed by the reaction were removed by a rotary evaporator condenser, and placed in a vacuum oven at 80°C for 24 hours, and the product was diglycolic anhydride. The yield was 93%.
[0167] The above diglycolic anhydride and 2.87g (11.9mmol) R 1 R 2 NH(R 1 , R 2 selected from isooctyl), which were dissolved in 20mL of dichloromethane organic solvent respectively; the two solutions were mixed and reacted at 25°C; during the reaction, the mixed solution gradually became clear, and when it was completely clear, the reaction Complete (about reaction 12h), make extraction agent shown in formula (I...
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