Tetravalent plutonium ion extraction method
An extraction and ion technology, which is applied in the field of extraction of tetravalent plutonium ions, can solve the problems of low efficiency, incomplete reduction of tetravalent plutonium, and complicated extraction process, and achieves fast extraction speed, good application prospects and strong extraction ability. Effect
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Embodiment 1
[0050] Preparation of extractant o-phenanthroline derivative C4-POPhen
[0051] The synthetic route of the present embodiment is as follows:
[0052]
[0053] The synthetic steps of the present embodiment include:
[0054] (1) Put 10mmol 2,9-dichloro-1,10-phenanthroline in 300mL toluene, add 24mmol dibutyl phosphite, 1mmol Pd(OAc) under stirring 2 , 2mmol of 1,1'-bis(diphenylphosphino)ferrocene and 24mmol of triethylamine to form a mixed solution, which was refluxed for 4 hours under the protection of nitrogen, and the reaction was tracked by thin-layer chromatography until the reaction of the raw materials was completely stopped.
[0055] (2) After the reaction is stopped, let it stand for cooling, remove solid impurities by suction filtration, and the filtrate is obtained by rotary evaporation to remove the solvent to obtain a crude product, which is obtained by CH 2 Cl 2 -MeOH system was used as eluent to separate and purify the obtained product by silica gel column c...
Embodiment 2
[0057] The organic phase and aqueous phase preparation of embodiment 2 extraction process
[0058] Preparation of the organic phase: C4-POPhen was dissolved in 3-nitrobenzotrifluorotoluene and mixed uniformly to form an organic phase, wherein the concentration of C4-POPhen was 0.01 mol / L.
[0059] The preparation of aqueous phase: get containing trace amount (about 10 -9 mol / L) radioactive element UO 2 (NO 3 ) 2 , 237 NPO 2 (NO 3 ) 2 and 242 Pu(NO 3 ) 4 The nitric acid aqueous solution is diluted with deionized water and added with quantitative concentrated nitric acid to prepare water phases with different nitric acid concentrations, wherein the nitric acid concentrations are 0.1, 0.5, 1.0, 2.0, 3.0 mol / L.
Embodiment 3-7
[0061] Take 0.5mL of aqueous phases with different concentrations of nitric acid, and carry out extraction reaction with an equal volume of organic phase, fully stir for 2 hours at a temperature of 293K, and perform centrifugal phase separation after reaching the extraction equilibrium. After phase separation, take 0.1mL of the extracted aqueous phase , the concentrations of U(VI), Np(V) and Pu(IV) in the aqueous phase were detected by liquid scintillation method.
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