Publications by authors named "Pavel Selucky"

Solvent extraction of microamounts of Eu3+ and Am3+ from water into nitrobenzene by means of a mixture of hydrogen dicarbollylcobaltate (H+B-) and N,N,N',N'-tetrabutyl-1,10-phenanthroline-2,9-dicarboxamide (L) was studied. The equilibrium data were explained assuming that the species HL+, H2L2+, HL+2, ML3+2, and ML3+3 (M3+ = Eu3+, Am3+; L = N,N,N',N'-tetrabutyl-1,10-phenanthroline-2,9-dicarboxamide) are extracted into the nitrobenzene phase. Extraction and stability constants of the cationic complex species in nitrobenzene saturated with water were determined and discussed.

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Extraction of microamounts of europium and americium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of dodecaethylene glycol (DDEG, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, H2L2+, ML3+ and MH-1L2+ (M3+ = Eu3+, Am3+; L = DDEG) are extracted into the organic phase. The values of extraction and stability constants of the complex species in nitrobenzene saturated with water have been determined.

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Extraction of microamounts of calcium and strontium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of 1,2-bis(diphenylphosphino)ethane dioxide (DPPEtDO, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL+2, ML2+2 and ML2+3 (M2+ = Ca2+, Sr2+) are extracted into the organic phase. The values of extraction and stability constants of the cationic complexes in nitrobenzene saturated with water have been determined.

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From extraction experiments and g-activity measurements, the exchange extraction constants corresponding to the general equilibrium M2+(aq) + 1•Sr2+(nb) <-> 1•M2+(nb) + Sr2+(aq) taking place in the two-phase water-nitrobenzene system (M2+ = Ca2+, Ba2+, Cu2+, Zn2+, Cd2+, Pb2+, UO22+, Mn2+, Co2+, Ni2+; 1 = p-tert-butylcalix[4]arene-tetrakis(N,N-diethylacetamide); aq = aqueous phase, nb = nitrobenzene phase) were determined. Further, the stability constants of the 1•M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.

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Extraction of microamounts of calcium and strontium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of N,N´-dimethyl-N,N´-diphenyl-2,6-dipicolinamide (MePhDPA, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL+2, ML2+2 and ML2+3 (M2+ = Ca2+, Sr2+) are extracted into the organic phase. The values of extraction and stability constants of the cationic complex species in nitrobenzene saturated with water have been determined.

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Extraction of microamounts of calcium and strontium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of bis(diphenylphosphino)methane dioxide (DPPMDO, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL2+, ML2(2+), ML3(2+) and ML4(2+) (M2+ = Ca2+, Sr2+) are extracted into the organic phase. The values of extraction and stability constants of the cationic complexes in nitrobenzene saturated with water have been determined.

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From extraction experiments and γ-activity measurements, the exchange extraction constantcorresponding to the general equilibrium Ca2+(aq) + 2HL(nb) <-> CaL2(nb) + 2H+(aq) taking place in the two-phase water-nitrobenzene (L- = anionic ligand based on cobalt bis(dicarbollide) anion with covalently bonded CMPO function; aq = aqueous phase, nb = nitrobenzene phase) was evaluated as log Kex (Ca2+, 2HL) = 0.0 ± 0.1.

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Extraction of microamounts of strontium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of N,N,N´,N´-tetracyclohexyl-oxybis(o-phenyleneoxy)diacetamide (abbrev. barium ionophore I, L) has been investigated. The equilibrium date have been explained assuming that the species HL+, SrL2+ and SrL2+2 are extracted into the organic phase.

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Solvent extraction of microamounts of calcium and strontium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of 2,6-(diphenylphosphino)pyridine dioxide (DPPPDO, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL+2, CaL2+2, CaL2+3, SrL2+2, SrL2+3 and SrL2+4 are extracted into the organic phase. The values of extraction and stability constants of the species in nitrobenzene saturated with water have been determined.

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From extraction experiments and g-activity measurements, the extraction constants corresponding to the general equilibrium Cs+(aq) + A- (aq) <-> Cs+(org) + A- (org) taking place in the two-phase water-phenyltrifluoromethyl sulfone (FS 13) system (A-= I-, ClO4-, MnO4-, Br-3, I-3, picrate, tetraphenylborate (BPh-4); aq = aqueous phase, org = FS 13 phase) were evaluated. Furthermore, the individual extraction constants of these 7 anions in the mentioned two-phase system were calculated; they were found to increase in the series of I-< ClO4- < Br-3 < MnO4-, picrate < I-3 < BPh-4.

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Solvent extraction of microamounts of europium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of 2, 6 - (diphenylphosphino)pyridine dioxide (DPPPDO, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL+2, EuL3+3 and EuL3+4 are extracted into the organic phase. The values of extraction and stability constants of the species in nitrobenzene saturated with water have been determined.

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Extraction of microamounts of strontium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of dibenzo-30-crown-10 (DB30C10, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, SrL2+, SrHL3+ and SrHL3+2 are extracted into the organic phase. The values of extraction and stability constants of the cationic complexes in nitrobenzene saturated with water have been determined.

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Extraction of microamounts of barium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of Slovafol 909 (L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL+2, BaL2+ and BaL2+2 are extracted into the organic phase. The values of extraction and stability constants of the complex species in nitrobenzene saturated with water have been determined.

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Solvent extraction of microamounts of calcium and strontium by a phenyltrifluoromethyl sulfone (FS 13) solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of octyl-phenyl-N,N-diisobutylcarbamoylmethyl phosphine oxide ("classical" CMPO, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL2+, ML2+, ML2+2 and ML2+3 (M2+ = Ca2+, Sr2+) are extracted into the organic phase. The values of extraction and stability constants of the cationic complex species in FS 13 saturated with water have been determined.

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Extraction of microamounts of cesium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of 2,3-naphtho-15-crown-5 (N15C5, L) has been investigated. The equilibrium data have been explained assuming that the complexes HL+, HL+2, CsL+ and CsL+2 are extracted into the organic phase. The values of extraction and stability constants of the species in nitrobenzene saturated with water have been determined.

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The covalent attachment of two CMPO-functions and two anionic Cosan groups to the narrow rim of tert-butylcalix[4]arene leads to a dramatic increase of the extraction efficiency for the cone isomer; Am(3+) is removed from 5 x 10(-8) M solution to more than 99% by a single extraction step with a 3 x 10(-6) M solution of the calixarene.

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