scholarly journals The Fluoride Complexes of Hafnium(IV). II. Determination of the Stability Constants by the Cation Exchange Method.

1967 ◽  
Vol 21 ◽  
pp. 2449-2456 ◽  
Author(s):  
Bertil Norén ◽  
Esko Taskinen ◽  
Pentti Salomaa ◽  
Gunnar Bloom ◽  
G. Hagen
2011 ◽  
Vol 76 (9) ◽  
pp. 1325-1336 ◽  
Author(s):  
Ivana Kostic ◽  
Tatjana Andjelkovic ◽  
Ruzica Nikolic ◽  
Aleksandar Bojic ◽  
Milovan Purenovic ◽  
...  

The stability of metal-humate complexes is an important factor determining and predicting speciation, mobility and bioavailability of heavy metals in the environment. A comparative investigation of the complexation of Cu(II) and Pb(II) with humic acid and humic-like ligands, such as benzoic and salicylic acid, was performed. The analysis was realized at pH 4.0, a temperature of 25?C and at an ionic strength of 0.01 (NaCl) using the Schubert ion-exchange method and its modified form. The stability constants were calculated from the experimental data by the Schubert method for complexes with benzoic and humic acid. A modified Schubert method was used for the determination of the stability constants of the complexes with salicylic acid. It was found that Cu(II) and Pb(II) form mononuclear complexes with benzoic and humic acid while with salicylic acid both metals form polynuclear complexes. The results indicate that Pb(II) has a higher binding ability than Cu(II) to all the investigated ligands. The Cu(II)-salicylate and Pb(II)-salicylate complexes showed noticeable higher stability constants compared with their complexes with humic acid, while the stabilities of the complexes with benzoic acid differed less. Salicylic and benzoic acids as humic-like ligands can be used for setting the range of stability constants of humic complexes with Cu(II) and Pb(II).


1971 ◽  
Vol 10 (4) ◽  
pp. 740-743 ◽  
Author(s):  
Leonard Newman ◽  
Paul Klotz ◽  
Anil Mukherji ◽  
Stephen Feldberg

1968 ◽  
Vol 21 (11) ◽  
pp. 2663 ◽  
Author(s):  
FM Hall ◽  
SJ Slater

The stability constants for the fluoride complexes of tin(11) have been determined by e.m.f. measurements, over a range of temperature, using both a tin amalgam electrode and the recently available fluoride ion activity electrode. The significance of the values ΔG -11480 cal/mole, ΔH 10350 cal mole-l, and ΔS 73.2 cal deg-1 mole-1 for the SnF3- complex is discussed and compared with those for the chloro and bromo complexes of tin(11).


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