Studies on the solvent extraction of metal dithiocarbamates

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.

1984 ◽  
Vol 62 (11) ◽  
pp. 2299-2301
Author(s):  
C. Mahalingam ◽  
J. K. Sthapak ◽  
D. D. Sharma ◽  
R. L. Tiwari ◽  
Smita Sthapak

The stability constants of metal complexes of 2-hydroxy-5-methylazobenzene-2′-carboxylic acid have been determined spectrophotometrically. These follow the Irving–Williams sequence: log KOH(H) = 10.67, log K1(Co) = 9.02, log K1(Ni) = 9.68, log K1(Cu) = 13.37, log K1(Zn) = 7.58, and [Formula: see text]The chelates of Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), and [Formula: see text] with the dye have been prepared and characterized on the basis of their ir and reflectance spectra.


2021 ◽  
Vol 14 (1) ◽  
pp. 54-63
Author(s):  
Yusuf Sabo ◽  
W.L.O. Jimoh ◽  
Isa Baba Koki ◽  
Q.O. Sholadoye

Stability constants of complexes of four divalent metal ions viz. Cu2+, Pb2+,Mg2+ and Cd2+  with humic acids (HA) were determined by potentiometric titration of humic acids with the corresponding salt of the divalent metals in aqueous media under non-acid-condition. The log K (logarithm of the stability constant) ranged from 1.0942 to 2.7471 for metal-humic acid complexes were determined using point-wise computational method. The order of stability constants were obtained as follows: Cu >Pb> Cd > Mg for metal -HA complexes respectively, indicating a higher degree of complexation with Cu metal ion. 


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.


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