Examination of the Conditions of Extraction of Toxic Organic Bases and of Methods of Their Determination. III. Extraction of Ion-Associates of Dibenz[b,f]-1,4-oxazepin

1994 ◽  
Vol 59 (3) ◽  
pp. 582-588
Author(s):  
Jan Souček ◽  
Ladislav Belický ◽  
Josef Havel
Keyword(s):  
Aqueous Phase ◽  
Basic Dye ◽  
Organic Bases ◽  
Safranine T ◽  
Extraction Constants ◽  
Distribution Constants

The protonation and distribution constants of dibenz[b, f]-1,4-oxazepin (CR) were measured. This substance forms stable ion-associates with Acid Red 88, extractable into chloroform. Reextraction with an aqueous phase containing basic fuchsine or safranine T brings about exchange of the CR cation for the basic dye cation. The associates so formed exhibit higher conditional extraction constants and higher molar absorptivities than the initial associates.

Extraction of Selected Organic Bases from Water into Chloroform by Means of the Cobaltacarborane Anion

1998 ◽  
Vol 63 (7) ◽  
pp. 967-976 ◽  
Author(s):  
Oldřich Navrátil ◽  
Zdeněk Skaličan ◽  
Zbyněk Kobliha ◽  
Emil Halámek
Keyword(s):  
Solvent Extraction ◽  
Aqueous Phase ◽  
Organic Nitrogen ◽  
Base Cations ◽  
Photometric Determination ◽  
Nitrogen Base ◽  
Organic Bases ◽  
Quaternary Salts ◽  
Extraction Constants

The cobaltacarborane anion labelled with 60Co was used to study the solvent extraction and stability of its ion associates with a series of organic nitrogen base cations or quaternary salts, some of which are psychoactive. The aqueous phase was 0.1 M HCl, the organic phase was chloroform. The extraction constants of the ion associates were calculated. A method was devised for competitive extraction of ion associates with additional dye anions which are used in the extraction-photometric determination of selected bases.

Extraction of scandium, cerium, promethium, and europium with dibutylphosphoric, bis(2-ethylhexyl)phosphoric, and dioctylphosphoric acids in Freon 113

1987 ◽  
Vol 52 (2) ◽  
pp. 322-328 ◽  
Author(s):  
Petr Linhart ◽  
Oldřich Navrátil ◽  
Josef Havel ◽  
Milan Vrchlabský
Keyword(s):  
Aqueous Solutions ◽  
Aqueous Phase ◽  
Acid Concentration ◽  
Organic Phase ◽  
Hydrogen Ions ◽  
Inorganic Acid ◽  
Extraction Constants ◽  
Distribution Constants ◽  
Phosphoric Acids

The extraction of Sc, Ce, Pm, and Eu from aqueous solutions of HClO4 and HNO3 into organic phases constituted by solutions of dialkylphosphoric acids in Freon 113 was studied. The effects of the kind of inorganic acid, concentration of hydrogen ions in the aqueous phase and concentration of the extracting agent in the organic phase were examined. Based on the dependences of the distribution ratios of the metals on the above variables, the compositions of the extractable complexes were determined and the extraction constants calculated. The dimerization constants and distribution constants of the monomer were also determined for dibutylphosphoric and bis(2-ethylhexyl)phosphoric acids.

Extraction of some metals into solutions of 1-phenyl-3-methyl-4-benzoylpyrazolone-5 in freon 113

1980 ◽  
Vol 45 (4) ◽  
pp. 1221-1226 ◽  
Author(s):  
Oldřich Navrátil ◽  
Pavel Linhart
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Stability Constants ◽  
Aqueous Phase ◽  
Organic Phase ◽  
Extraction Constants ◽  
Distribution Constants ◽  
The Stability

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.

Extraction of hafnium by means of some substituted 1-phenyl-3-methyl-4-benzoyl-pyrazol-5-ones

1981 ◽  
Vol 46 (8) ◽  
pp. 1901-1905 ◽  
Author(s):  
Oldřich Navrátil ◽  
Jiří Smola
Keyword(s):  
Ionic Strength ◽  
Aqueous Phase ◽  
Dissociation Constants ◽  
Parent Substance ◽  
Benzoyl Group ◽  
Extraction Constants ◽  
Extraction Parameters ◽  
Substituted 1

Distribution between aqueous phase and benzene or chloroform was studied for 1-phenyl-3-methyl-4-benzoylpyrazol-5-ones with 2-chloro, 4-methoxy, 3-nitro, and 4-nitro substitution in the benzoyl group (ionic strength of the aqueous phase 0.1) and for hafnium in their presence (ionic strength 2.0). The distribution and dissociation constants of the reagents and the extraction constants of their hafnium complexes were determined. Hafnium was found to be extracted as the HfA4 species. The extraction parameters of the derivatives in question do not differ substantially from those of the parent substance.

Extraction of rare earth metals from trichloroacetate solutions in the presence of linear polyoxonium compounds

1991 ◽  
Vol 56 (8) ◽  
pp. 1585-1592 ◽  
Author(s):  
Petr Vaňura
Keyword(s):  
Rare Earth ◽  
Nonionic Surfactant ◽  
Separation Factor ◽  
Rare Earth Metals ◽  
Extraction Constants ◽  
Distribution Constants ◽  
Factor Α

Extraction of rare earth metals from lithium trichloroacetate solutions ( 1.20-2.88 mol l-1) with solutions of the commercial nonionic surfactant Slovafol 909 (p-nonylphenylnonaethylene glycol) in chloroform and dichloromethane was investigated. The extraction constants as well as the Slovafol 909 distribution constants were determined in the water-dichloromethane and water-chloroform systems. The lanthanide distribution ratios decrease with their atomic numbers first rather rapidly (approximately to Sm): the separation factor αSmLa = 1.54 and 1.87 in dichloromethane and in chloroform, respectively; for lanthanides with higher atomic numbers the drop is less pronounced (αLuLa = 2.42 and 2.85 in the two solvents, respectively).

Extraction of cadmium salicylate with some nitrogen-containing organic bases

1978 ◽  
Vol 56 (23) ◽  
pp. 2922-2926 ◽  
Author(s):  
J. M. Singh ◽  
S. N. Tandon
Keyword(s):  
Synergistic Effect ◽  
Aqueous Solutions ◽  
Experimental Conditions ◽  
Organic Bases ◽  
Distribution Constants ◽  
Coordinated Water

Cd(HSal)2 is extracted from aqueous solutions into n-butanol, but not into non-hydroxylic solvents (such as benzene and chloroform) at pH 4.5 to 6.0. Addition of N bases, which have no effect alone, causes extraction into the latter solvents, apparently by displacement of coordinated water, giving Cd(HSal)2•2B. This synergistic effect varies with B (β-picoline > pyridine > quinoline). Formation and distribution constants are given for the experimental conditions.

Thermodynamics of Solvent Extraction of Perrhenate with N235 at High Concentration

2010 ◽  
Vol 150-151 ◽  
pp. 890-894
Author(s):  
Ke Xu Jiang ◽  
Da Wei Fang ◽  
Han Wang ◽  
Bao Xin Wang ◽  
Ying Xiong ◽  
...  
Keyword(s):  
Solvent Extraction ◽  
Aqueous Phase ◽  
Supporting Electrolyte ◽  
Extraction Process ◽  
Extraction System ◽  
Thermodynamic Quantities ◽  
High Concentration ◽  
Extraction Constants ◽  
Solvent Extraction System

In solvent extraction system of perrhenate with the extractant of N235 at high concentration, the equilibrium molalities of ReO4- were measured at ionic strengths from 0.2 to 2.0 mol.kg-1 in the aqueous phase containing Na2SO4 as the supporting electrolyte from 278.15K to 303.15K. The standard extraction constants K0 at various temperatures were obtained. Thermodynamic quantities for the extraction process were also calculated.

Extraction of iron(III) from the citric medium by the toluene solution of trilaurylamine

1980 ◽  
Vol 45 (11) ◽  
pp. 3116-3129 ◽  
Author(s):  
Petr Vaňura ◽  
Libor Kuča
Keyword(s):  
Citric Acid ◽  
Ionic Strength ◽  
Aqueous Phase ◽  
Organic Phase ◽  
Toluene Solution ◽  
Constant Ionic Strength ◽  
Extraction Constants ◽  
Equilibrium Concentrations

The composition of Fe(III) complexes extracted from the aqueous phase of constant ionic strength (1M-(H3,Na3,Fe)A, where H3A denotes citric acid) by the toluene solution of trilaurylamine (TLA) has been determined and the respective extraction constants have been calculated. In the concentration range cFe < 10-2 mol l-1 FeA(TLA)2 and FeA(TLA)4(H3A)2-4 are the predominant complexes in the organic phase. The abundance of the (FeA)3(TLA)6(H3A)2 complex in the organic phase increases at higher equilibrium concentrations of Fe(III) in the aqueous phase and at higher concentrations of TLA.

Extraction of Selected Lanthanoids and Scandium with Bis(2-ethylhexyl)hydrogenphosphate in 1,1,2,2-Tetrachlorodifluoroethane

1992 ◽  
Vol 57 (8) ◽  
pp. 1647-1654 ◽  
Author(s):  
Petr Sládek ◽  
Oldřich Navrátil ◽  
Petr Linhart
Keyword(s):  
Solid Phase ◽  
Metal Chelates ◽  
Organic Medium ◽  
Extraction Constants ◽  
Distribution Constants ◽  
The Individual

A study was made of the extraction of Ce, Pm, Eu, Tm and Sc(III) from aqueous into organic medium of 1,1,2,2-tetrachlorodifluoroethane (CFC-112) using bis(2-ethylhexyl)hydrogenphosphate (HDEHP) as extracting reagent. On the basis of earlier work which demonstrated the usefulness of using this type of solvent for extractions with dibutylhydrogenphosphate (HDBP) and also the possibility of using CFC-112 for converting the metal chelates formed to the solid phase, the work was concentrated particularly on the dependence of the extraction of selected lanthanoids on the analytical concentration of HDEHP and also on the [H+] concentration. In addition the dimerization and distribution constants were determined for this reagent in a mixture of CFC-112 with benzene and the extraction constants were determined for the individual metals.

Investigation of the Conditions of Extraction of Ion-Associates of 3-Quinuclidinyl Benzilate with Acidic Dyes

1993 ◽  
Vol 58 (2) ◽  
pp. 315-319 ◽  
Author(s):  
Emil Halámek ◽  
Zbyněk Kobliha
Keyword(s):  
Aqueous Phase ◽  
Bromocresol Green ◽  
Limits Of Detection ◽  
Extraction Constants ◽  
Optimum Ph ◽  
Metanil Yellow ◽  
Quinuclidinyl Benzilate

Ion-associates of 3-quinuclidinyl benzilate (BZ) with thirteen acidic dyes were examined after their extraction into chloroform. Based on spectrophotometric measurements, the optimum pH of the aqueous phase was established and the extraction yields, distribution ratios, conditional extraction constants and limits of detection were calculated. Bromocresol green and metanil yellow are suggested as reagents for the analysis of BZ.

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