Calix[4]arene-crown-5 as a selective extraction reagents for K+/H+, Rb+/H+ and Rb+/Cs+ separations

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Petr Vaňura ◽  
Emanuel Makrlík ◽  
Pavel Selucký

Abstract From extraction experiments, the exchange extraction constants corresponding to the general equilibriums M+ (aq) + NaL+ (org) ⇔ ML+ (org) + Na+ (aq) or M+ (aq) + CsL+ (org) ⇔ ML+ (org) + Cs+ (aq), which take place in the two-phase water–nitrobenzene extraction system (M+ = Li+, H3O+, Ag+, K+, NH4 +, Tl+, Rb+; L = calix[4]arene-bis crown5(1,3-alternate), 26,28-dipropoxycalix[4]arene-crown-5(1,3-alternate), 11,23-dibromo-25,28-dipropoxycalix[4]arene-crown-5 (1,3-alternate) and 1,3-alternate-25,27-dihydroxycalix[4]arene-crown-5; aq = aqueous phase, org = organic phase), were evaluated. The stability constants of the NaL+ and CsL+ complexes were calculated from the extraction of the respective picrates in the system of water–nitrobenzene solution of L. Further, the stability constants of the ML+ complexes in nitrobenzene saturated with water were determined. High selectivities were found in some systems under study.

2006 ◽  
Vol 71 (11) ◽  
pp. 1147-1151 ◽  
Author(s):  
E. Makrlík ◽  
P. Vaňura

From extraction experiments and ?-activity measurements, the exchange extraction constant corresponding to the equilibrium Ba2+(aq) + SrL2 2+(nb) _ BaL 2 2+(nb) + Sr2+(aq) occurring in the two-phase water-nitrobenzene system (L = benzo-15-crown-5; aq = aqueous phase, nb = nitrobenzene phase) was evaluated as log K ex (Ba2+, SrL22+) = 0.3 ? 0.1. Furthermore, the stability constant of the benzo-15-crown-5-barium complex in nitrobenzene saturated with water was calculated for the temperature of 25 ?C: log ?nb (BaL2 2+) = 13.3?0.1.


2009 ◽  
Vol 74 (7) ◽  
pp. 781-787 ◽  
Author(s):  
Emanuel Makrlík ◽  
Petr Vaňura ◽  
Pavel Selucký ◽  
Vasily Babain ◽  
Ivan Smirnov

Extraction of micro-amounts of europium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of N,N'-dimethyl- -N,N'-diphenyl-2,6-dipicolinamide (MePhDPA, L) was investigated. The equilibrium data were explained assuming that the species HL+, + HL2 , 3+ EuL2 and 3+ EuL3 are extracted into the organic phase. The values of the extraction and stability constants of the species in nitrobenzene saturated with water were determined.


2008 ◽  
Vol 73 (12) ◽  
pp. 1181-1186 ◽  
Author(s):  
E. Makrlík ◽  
J. Budka ◽  
P. Vaňura ◽  
P. Selucký

The exchange extraction constants corresponding to the general equilibrium M2+(aq) + SrL2+(nb) ? ?ML2+(nb) + Sr2+(aq) occurring in the two- -phase water-nitrobenzene system (M2+ = Ca2+, Ba2+, Cu2+, Zn2+, Cd2+, Pb2+, UO22+ , Mn2+, Co2+ or Ni2+; L = tetra-tert-butyl p-tert-butylcalix[4]arene tetraacetate; aq = aqueous phase; nb = nitrobenzene phase) were evaluated from extraction experiments and ?-activity measurements. Furthermore, the stability constants of the ML2+ complexes in water saturated nitrobenzene were calculated; they were found to increase in the cation order Ba2+ < Mn2+ < Pb2+, Co2+ < Cu2+, Zn2+ < Cd2+, Ni2+ < UO22+ < Ca2+.


1980 ◽  
Vol 45 (4) ◽  
pp. 1221-1226 ◽  
Author(s):  
Oldřich Navrátil ◽  
Pavel Linhart

The partition of 1-phenyl-3-methyl-4-benzoylpyrazolone-5 (HA) between aqueous solutions of HClO4 and NaClO4, ionic strength 0.1, and Freon 113 or its 2 : 1 mixture with benzene was studied. The logarithms of the HA distribution constants are 2.84 ± 0.10 and 3.39 ± 0.15 for the two organic phases, respectively. The extraction curves of cerium(III) and europium(III) revealed that in dependence on the pH of the aqueous phase, the metals are transferred into the organic phase in the form of the MA3 complexes (M = Ce, Eu). The stability constants of the complexes MAn in the aqueous phase were determined along with their distribution and extraction constants. For cobalt, zinc, and hafnium, a part of the extraction curves could only be studied, only the extraction constants were therefore determined. The sparing solubility of HA in Freon 113 can be circumvented by using a Freon-benzene mixture 2 : 1, which is still practically incombustible.


1985 ◽  
Vol 50 (3) ◽  
pp. 581-599 ◽  
Author(s):  
Petr Vaňura ◽  
Emanuel Makrlík

Extraction of microamounts of Sr2+ and Ba2+ (henceforth M2+) from the aqueous solutions of perchloric acid (0.0125-1.02 mol/l) by means of the nitrobenzene solutions of dicarbolide (0.004-0.05 mol/l of H+{Co(C2B9H11)2}-) was studied in the presence of monoglyme (only Ba2+), diglyme, triglyme, and tetraglyme (CH3O-(CH2-CH2O)nCH3, where n = 1, 2, 3, 4). The distribution of glyme betweeen the aqueous and organic phases, the extraction of the protonized glyme molecule HL+ together with the extraction of M2+ ion and of the glyme complex with the M2+ ion, i.e., ML2+ (where L is the molecule of glyme), were found to be the dominating reactions in the systems under study. In the systems with tri- and tetraglymes the extraction of H+ and M2+ ions solvated with two glyme molecules, i.e., the formation of HL2+ and ML22+ species, can probably play a minor role. The values of the respective equilibrium constants, of the stability constants of complexes formed in the organic phase, and the theoretical separation factors αBa/Sr were determined. The effect of the ligand structure on the values of extraction and stability constants in the organic phase is discussed.


2000 ◽  
Vol 65 (4) ◽  
pp. 275-279
Author(s):  
Marcela Danková ◽  
Emanuel Makrlík ◽  
Petr Vanura

From extraction experiments and g-activity measurements, the extraction constant corresponding to the equilibrium Ca 2+ (aq)+ SrL 2+ (nb) === CaL 2+ (nb) + Sr 2+ (aq) taking place in the two-phase water-nitrobenzene system(L= 18-crown-6, aq = aqueous phase, nb = nitrobenzene phase) was evaluated as log Kex(Ca 2+, SrL 2+) = -1.9 ?0.1. Furthermore, the stability constant of the calcium - 18-crown-6 complex in nitrobenzene saturated with water was calculated for the temperature of 25?C: log bnb (CaL 2+)=10.1?0.1.


2012 ◽  
Vol 10 (5) ◽  
pp. 1495-1499
Author(s):  
Emanuel Makrlík ◽  
Petr Vaňura ◽  
Pavel Selucký

AbstractFrom extraction experiments and γ-activity measurements, the exchange extraction constants corresponding to the general equilibrium C+(aq) + 1·Na+(nb) 1·C+ (nb) + Na+(aq) taking place in the two-phase water-nitrobenzene system (C+ = methylammonium, ethylammonium, propylammonium, ethanolammonium, diethanolammonium, triethanolammonium, cation TRIS+, hydrazinium, hydroxylammonium; 1 = benzo-18-crown-6; aq = aqueous phase, nb = nitrobenzene phase) were evaluated. Furthermore, the stability constants of the 1·C+ cationic complex species in nitrobenzene saturated with water were calculated; they were found to increase in the following cation order: triethanolammonium +


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