scholarly journals ELECTRODEPOSITION OF COPPER IN ULTRASONIC FIELD FROM SPENT ETCHING SOLUTIONS

Author(s):  
Maria P. Larionova ◽  
Nina D. Solovieva ◽  
Elena A. Savelieva

It is studied the regeneration and utilization possibility of spent nitric acid solutions for copper and its alloys etching for the creating an environmentally clean closed-cycle production of regenerated electrolytes. It is established that some difficulties arise when using the electrochemical method in the regeneration process of these solutions: during copper electrodeposition from spent copper-containing nitric acid solutions, nitric acid decomposes with vigorous evolution of nitrogen dioxide, which prevents copper ions reduction. In order to suppress the side process, it was proposed to partially neutralize the solution, not reaching the pH of copper hydration (pH 4-5). It is revealed that a decrease in the concentration of metal cations occurs due to partial neutralization of the nitric acid contained in the solution by concentrated alkali solution. The pulsed electrolysis mode was used to increase the efficiency of the metal ions electrodeposition process from dilute solutions. It is established that the using of pulsed electrolysis can reduce diffusion difficulties that arise in a dilute spent nitric acid copper-containing solution, thereby intensify the process of copper electrodeposition. It is showed that the prospects of using ultrasound to increase the rate of the copper electrodeposition process and improve the quality of the resulting coating. It is studied the ultrasound field effect on nucleation during copper electrodeposition in a pulsed mode from a partially neutralized electrolyte simulating the spent nitrate solution of etching copper alloys on various materials by the potentiostatic. It is established an increase in the number of copper nucleus that form on the studied substrates (graphite, copper, steel) at the initial time under the action of an ultrasonic field. It is concluded that the use of ultrasound allows to intensify the process of metal electrodeposition. An increase in current efficiency during copper electrodeposition and an increase in the copper extraction degree using ultrasonic field are achieved at lower cathodic current densities in a pulse. It is substantiated using of graphite foil and steel as cathode materials in the copper extraction from the spent nitric acid etching solution.

2020 ◽  
Vol 108 (9) ◽  
pp. 707-716
Author(s):  
Jarrod M. Gogolski ◽  
Peter R. Zalupski ◽  
Travis S. Grimes ◽  
Mark P. Jensen

AbstractSeparation of neptunium by solvent extraction has been based on tributylphosphate (TBP) for decades, but TBP is not fully incinerable, which adds to the burden of long-lived radioactive waste. Alternatives to TBP for uranium and plutonium extraction, such as the N,N-diakylamides, previously have been explored in the hopes of transitioning to an extractant that is incinerable. Four N,N-diakylamides, N,N-dihexylhexanamide (DHHA), N,N-dihexyloctanamide (DHOA), N,N-di(2-ethylhexyl)butanamide (DEHBA), and N,N-di(2-ethylhexyl)-iso-butanamide (DEHiBA) were considered in this work for their potential to extract millimolar concentrations of Np(IV), Np(V), and Np(VI) from nitric acid solutions into organic solutions containing 1 M extractant in Exxsol D60. Under these conditions the branching of the alkyl substituents affects the extractability of Np(VI) and Np(IV), causing three of the dialkylamides, DHHA, DHOA and DEHBA, to extract neptunium in the expected order Np(VI) > Np(IV) > > Np(V). In contrast, branched DEHiBA is so poor an extractant for Np(IV) that the extraction order becomes Np(VI) > > Np(V) > Np(IV) between 0.1 and 5.6 M HNO3 due to partial oxidation of the Np(V) in nitric acid.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Rajesh B. Gujar ◽  
Parveen K. Verma ◽  
Prasanta K. Mohapatra ◽  
Mudassir Iqbal ◽  
Jurriaan Huskens ◽  
...  

Abstract Neptunium is one of the most important minor actinide elements with some of its isotopes having very long half-lives, therefore necessitating its separation from acidic radioactive wastes. Solvent extraction of Np4+ and NpO2 2+ was studied using three multiple diglycolamide (DGA) extractants with n-propyl, n-octyl and 3-pentyl substituents termed as L I , L II and L III , respectively, in a mixed diluent of 5% isodecanol and 95% n-dodecane. For comparison purpose, the extraction of Pu4+ and UO2 2+ was carried out under identical conditions. The extraction efficiency of the ligands for the tetravalent ions followed the trend: L II  > L I  > L III , which changed to L III  > L II  > L I for the hexavalent ions. While the extraction of the tetravalent ions was reasonably good (ca. 90–98%) with an extremely low (5.0 × 10−5 M) ligand concentration, poor extraction (ca. 5–16%) of the hexavalent ions was seen even with a 20 times higher concentration of the ligand. In general, Pu4+ was better extracted than Np4+, while NpO2 2+ was marginally better extracted then UO2 2+. A ‘solvation’ type extraction mechanism was proposed based on the extraction profiles obtained as a function of the concentrations of the feed nitric acid, extractant as well as nitrate ion. The extracted species were found out to be M(NO3)4·mL and MO2(NO3)2·nL (M = Np or Pu, 1 < m < 2, n ≃ 1).


2020 ◽  
Vol 62 (5) ◽  
pp. 581-586
Author(s):  
Yu. M. Kulyako ◽  
D. A. Malikov ◽  
T. I. Trofimov ◽  
S. A. Perevalov ◽  
K. S. Pilyushenko ◽  
...  

Author(s):  
Joseph L Lapka ◽  
Alena Paulenova ◽  
Mikhail Yu Alyapyshev ◽  
Vasiliy A Babain ◽  
Jack D Law ◽  
...  

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