scholarly journals On an Expression of Extraction Constants without the Interfacial Equilibrium-Potential Differences for the Extraction of Univalent and Divalent Metal Picrates by Crown Ethers into 1,2-Dichloroethane and Nitrobenzene

2015 ◽  
Vol 06 (04) ◽  
pp. 350-363 ◽  
Author(s):  
Yoshihiro Kudo ◽  
Shoichi Katsuta
1969 ◽  
Vol 47 (12) ◽  
pp. 2320-2323 ◽  
Author(s):  
Vedula S. Sastri ◽  
Keijo I. Aspila ◽  
Chuni L. Chakrabarti

Studies on the solvent extraction of morpholine dithiocarbamic acid complexes of divalent metal ions Mn, Fe, Co, Ni, Cu, Zn, Pb, Cd, Hg, and Sn were carried out, and the extraction constants and the overall stability constants were determined. The stability constants of complexes of Cu(II) formed with various substituted dithiocarbamic acids, showed a variation of the stability constants with the basicity of the nitrogen and sulfur atoms in the reagents.


2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Yoshihiro Kudo ◽  
Tsubasa Nakamori ◽  
Chiya Numako

Individual distribution constants (KD,A) of picrate ion (Pic−) and extraction constants (Kex±) of NaPic by some crown ethers (L) into benzene (Bz) at 25°C were calculated from data reported previously. These constants were defined asKD,Pic=Pic-o/[Pic-]andKex±=NaL+oPic-o/(Na+Lo[Pic-]), respectively. Here, the subscript “o” denotes an organic (o) phase and practically o = Bz. 15-Crown-5 ether (15C5), 18-crown-6 one (18C6), and their monobenzo (B) derivatives (B15C5 and B18C6) were selected as L. Interfacial equilibrium-potential differences (Δϕeq) at extraction were estimated at 298 K. A plot oflog⁡Kex±versus-Δϕeqfor the four L extraction systems gave a straight line with slope = 84 V−1. This slope was compared with those, reported before, of the dichloromethane (DCM), 1,2-dichloroethane (DCE), and nitrobenzene (NB) extraction systems. The slopes of the regression lines were in the order NB < DCM ≤ DCE < Bz. Also, the individual distribution constants of the complex ionNaL+and an ion-pair complex (NaL+Pic-) into Bz phase were calculated from the above extraction data. At least, a comparison between these values suggests that Bz molecules mainly interact withNaL+moiety ofNaL+Pic-.


1987 ◽  
Vol 65 (4) ◽  
pp. 884-891 ◽  
Author(s):  
Thomas Murray Fyles

A method is described for the estimation of two phase extraction constants from stability constants for complexation of alkali metal cations by crown ethers and cryptands. The total free energy change for extraction of alkali metal salts from water to a non-polar organic solvent is evaluated as a sum of free energy terms for complexation, transfers of cation, anion, and complex between solvents, and ion pairing in the non-polar solvent. The method gives satisfactory agreement with a variety of published extraction constants and can be used predictively. As an example, the influence of extraction constant on transport flux was examined using calculated extraction constants and the rate data of Lamb etal. (J. Am. Chem. Soc. 102, 6820 (1980)); rates are adequately modelled by a simple analysis of diffusion.


2017 ◽  
Vol 9 (4) ◽  
pp. 110 ◽  
Author(s):  
Yoshihiro Kudo ◽  
Tomohiro Amano ◽  
Satoshi Ikeda

Extraction constants (Kex± & Kex) were determined at 298 K for the extraction of sodium picrate (NaPic) by nitrobenzene (NB), 1,2-dichloroethane (DCE) and dichloromethane using 3m-crown-m ethers and their benzo-derivatives (m = 5, 6; abbreviated as L) together with the determination of conditional distribution constants (KD,Pic) of picrate ion, Pic-, into these diluents. The K1,org (= [NaLPic]org/[NaL+]org[Pic-]org) values at the organic (org) phases, such as NB & DCE, were calculated from the relation Kex/Kex± = K1,org. Distribution equilibrium-potential differences (Dfeq) at extraction equilibria were evaluated from the equation Dfeq = -0.05916´(log KD,Pic - constant) at 298 K. Correlations of the above equilibrium constants, particularly Kex±, with Dfeq were examined. Furthermore, the standard formal potentials for Na+ transfers across the interfaces were briefly evaluated from calculated Dfeq, [Na+] and [Pic-]org. The above extraction systems were characterized by K1,org and the complex formation constants of Na+ with L in the org phases.


Inorganics ◽  
2018 ◽  
Vol 6 (3) ◽  
pp. 77 ◽  
Author(s):  
Yoshihiro Kudo ◽  
Tsubasa Nakamori ◽  
Chiya Numako

Extraction of Pb(II) with picrate ion [Pic−] and 0, 0.58, 15, 48, or 97 mmol dm−3 Cd(NO3)2 by benzo-18-crown-6 ether (B18C6; L as its symbol) into benzene (Bz) was studied. Three kinds of extraction constants, Kex, Kex±, and KPb/PbL (or Kex2±), were determined at 298 K: these constants were defined as [PbLPic2]Bz/P, [PbLPic+]Bz[Pic−]Bz/P, and [PbL2+]Bz/[Pb2+][L]Bz (or [PbL2+]Bz([Pic−]Bz)2/P), respectively. The symbol P shows [Pb2+][L]Bz[Pic−]2 and the subscript “Bz” denotes the Bz phase, Bz saturated with water. Simultaneously, conditional distribution constants, KD,Pic (=[Pic−]Bz/[Pic−]), of Pic− with distribution equilibrium-potential differences (dep) were determined. Then, based on the above four constants and others, the component equilibrium constants of K1,Bz (=[PbLPic+]Bz/[PbL2+]Bz[Pic−]Bz), K2,Bz (=[PbLPic2]Bz/[PbLPic+]Bz[Pic−]Bz), and KD,PbL (=[PbL2+]Bz/[PbL2+]) were obtained. Using these constants, the Pb(II) extraction with B18C6 under the co-presence of Cd(II) in the water phase was characterized. In such a characterization, I and IBz dependences on the constants were mainly discussed, where their symbols denote the ionic strength of the water phase and that of the Bz one, respectively.


1991 ◽  
Vol 81 (4) ◽  
pp. 462-466 ◽  
Author(s):  
Maria Fabiana Drincovich ◽  
Alberto A. Iglesias ◽  
Carlos S. Andreo

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