Water—organic solvent systems in countercurrent chromatography: Liquid stationary phase retention and solvent polarity

Talanta ◽  
1993 ◽  
Vol 40 (10) ◽  
pp. 1489-1498 ◽  
Author(s):  
Alain Berthod ◽  
Nathalie Schmitt
2006 ◽  
Vol 48 (3) ◽  
pp. 284-287
Author(s):  
M. N. Litvina ◽  
D. A. Malikov ◽  
T. A. Maryutina ◽  
Yu. M. Kulyako ◽  
B. F. Myasoedov

2005 ◽  
Vol 93 (1) ◽  
Author(s):  
B. F. Myasoedov ◽  
T. A. Maryutina ◽  
M. N. Litvina ◽  
D. A. Malikov ◽  
Yu. M. Kulyako ◽  
...  

AbstractThe separation of Am(III) and Cm(III) by countercurrent chromatography (CCC) was achieved using the liquid phase systems "diamide–hydrogenated tetrapropylene (TPH)–HNOThe following diamide extractants have been studied: (i) N,N´-dimethyl-N,N´-dibutyltetradecylmalonamide (DMDBTDMA), (ii) N,N´-dimethyl-N,N´-dioctylhexyl-ethoxymalonamide (DMDOHEMA) and (iii) N,N´-dimethyl-N,N´-dibutyldodecylethoxymalonamide (DMDBDDEMA). It is shown that these diamides can be used for the separation of Am(III) and Cm(III) by CCC. Increasing the column length leads to an increase of the stationary phase retention on the column while improving the Am/Cm separation. Increasing the speed of rotation of the centrifuge from 660 to 950 rpm also results in increasing the stationary phase retention but does not influence the resolution of the Am/Cm separation. Decreasing the flow rate of the mobile phase from 1.0 to 0.5 mL/min leads to a better resolution of Am and Cm separation. The best Am/Cm separation was achieved with systems based on DMDBDDEMA and DMDOHEMA in TPH using a two-layer coil column and an isocratic elution mode. The application of CCC makes it possible to separate the elements within 100 min: the Cm fraction contains 99.5% of Cm(III) and 0.6% of Am(III) inventories and the Am fraction contains 99.4% of Am(III) and 0.5% of Cm(III).


2009 ◽  
Vol 81 (2) ◽  
pp. 355-387 ◽  
Author(s):  
Alain Berthod ◽  
Tatyana Maryutina ◽  
Boris Spivakov ◽  
Oleg Shpigun ◽  
Ian A. Sutherland

Countercurrent chromatography (CCC) is a generic term covering all forms of liquid-liquid chromatography that use a support-free liquid stationary phase held in place by a simple centrifugal or complex centrifugal force field. Biphasic liquid systems are used with one liquid phase being the stationary phase and the other being the mobile phase. Although initiated almost 30 years ago, CCC lacked reliable columns. This is changing now, and the newly designed centrifuges appearing on the market make excellent CCC columns. This review focuses on the advantages of a liquid stationary phase and addresses the chromatographic theory of CCC. The main difference with classical liquid chromatography (LC) is the variable volume of the stationary phase. There are mainly two different ways to obtain a liquid stationary phase using centrifugal forces, the hydrostatic way and the hydrodynamic way. These two kinds of CCC columns are described and compared. The reported applications of CCC in analytical chemistry and comparison with other separation and enrichment methods show that the technique can be successfully used in the analysis of plants and other natural products, for the separation of biochemicals and pharmaceuticals, for the separation of alkaloids from medical herbs, in food analysis, etc. On the basis of the studies of the last two decades, recommendations are also given for the application of CCC in trace inorganic analysis and in radioanalytical chemistry.


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