Third phase formation behaviour of tris(2-methylbutyl) phosphate and tri-n-alkyl phosphates in the extraction of mineral acids and tetravalent metal ions

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Subramee Sarkar ◽  
A. Suresh ◽  
N. Sivaraman

Abstract The formation of third phase is a detrimental phenomenon witnessed in the nuclear separation processes during the extraction of certain metal salts by an organic solution, which comprises of a neutral extractant, tri-n-butyl phosphate dispersed in a non-polar diluent, n-dodecane (n-C12H26). In the present work, a comparative analysis on the third phase formation behaviour of three trialkyl phosphates, TBP, its linear and branched higher homologues tri-n-amyl phosphate and tris(2-methylbutyl) phosphate (T2MBP), respectively, have been provided which will be useful for the identification of an extractant with minimum third phase formation tendency. The organic phase splitting behaviour during the extraction of three mineral acids (HClO4, HCl and HNO3) and two tetravalent metal nitrates (Th(IV) and Zr(IV)) by trialkyl phosphates has been investigated to understand the influence of anionic and cationic components, respectively, in third phase formation of trialkyl phosphates. The effect of structure of the alkyl groups of trialkyl phosphate and chain length of diluents on third phase formation during Zr(IV) extraction from HNO3 media have also been studied. Overall, the third phase formation behaviour of T2MBP was found to be lower both for the extraction of mineral acid and Zr(IV), thereby indicating its potentiality for applications in various solvent extraction processes.

2008 ◽  
Vol 96 (4-5) ◽  
Author(s):  
Fabienne Testard ◽  
Pierre Bauduin ◽  
L. Martinet ◽  
B. Abécassis ◽  
L. Berthon ◽  
...  

A review of the four microstructures present in oil phases of malonamide extractants used for nuclear fuel reprocessing is presented in relation with the extraction properties and the third phase formation. Due to their surface active properties, extractants can be considered as a weak surfactants and are organised into reverse micelles interacting through an attractive potential. The Van der Waals attractions between the cores of reverse micelles are the key parameters for understanding “third phase” formation. Extractant solutions are similar to reverse microemulsions and the stability rules known in the field of microemulsions can be applied. In some cases, micelles are transformed into a regular molecular solution by modest heating. Apart from micellar and regular solutions, two new modes of association of extractant molecules have been identified. Networks of H-bounds are obtained when “modifiers” such as octanol are added by formulators in order to improve stability range. Microphase separation in a more crystalline phase may be obtained by increasing extractant and/or ion concentrations.


2017 ◽  
Vol 105 (4) ◽  
Author(s):  
Aditi Chandrasekar ◽  
A. Suresh ◽  
N. Sivaraman

AbstractEarlier studies carried out in our laboratory indicated that Tri-sec-butyl phosphate (TsBP) is a potential extractant for U/Th separation. Also, the third phase formation tendency of TsBP is lower compared to its isomers, Tri-


1998 ◽  
Vol 16 (4) ◽  
pp. 1001-1011 ◽  
Author(s):  
T.G. Srinivasan ◽  
S. Vijayasaradhi ◽  
R. Dhamodaran ◽  
A. Suresh ◽  
P.R. Vasudeva Rao

2011 ◽  
Vol 99 (3) ◽  
pp. 179-186 ◽  
Author(s):  
K. V. Lohithakshan ◽  
V. K. Aswal ◽  
S. K. Aggarwal

2007 ◽  
Vol 95 (8) ◽  
Author(s):  
A. Suresh ◽  
R. Deivanayaki ◽  
T. G. Srinivasan ◽  
P. R. Vasudeva Rao

In the above mentioned paper we had reported a non-linear dependence of limiting organic concentration (LOC) with temperature in the case of tri-2-methyl butyl phosphate in n-tetradecane as well as n-hexadecane diluents. Subsequently we extended the studies to other trialkyl phosphates such as TBP, TiBP, TsBP, TAP, TiAP and TsAP in various diluents (n-decane, n-dodecane, n-tetradecane, n-hexadecane and n-octadecane) and found recently that the dependence was always linear, irrespective of the extractant-diluent combination. This behaviour urged us to have a thorough review of the data reported earlier and when we repeated the studies again in the same systems, we found that the dependence was only linear and not as reported earlier.We have critically looked into what went wrong in the earlier studies and at present have concluded that wrong temperature calibration/measurement might have induced the same.We now present the correct data in Tables 1 and 2 and 4. Some parts of the sections “Results and discussion” and “Conclusions” are also modified.


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