Speciation of low molecular weight carboxylic ligands in natural fluids: protonation constants and association with major components of seawater of oxydiacetic and citric acids
C. De Stefano et al., Speciation of low molecular weight carboxylic ligands in natural fluids: protonation constants and association with major components of seawater of oxydiacetic and citric acids, ANALYT CHIM, 398(1), 1999, pp. 103-110
The interaction of oxydiacetate and citrate with the major components of se
awater has been studied potentiometrically, at 25 degrees C, in an artifici
al seawater (containing Na+, K+, Ca2+, Mg2+, Cl- and SO42-) at different sa
linities (5-45 parts per thousand). Apparent protonation constants were cal
culated, from potentiometric data, and estimated, using an appropriate comp
lex formation model. Formation constants of complexes formed by oxydiacetat
e and citrate and the cation of seawater (the inorganic content of seawater
being considered as a single 1:1 salt) were determined. The single salt ap
proximation for the major inorganic components of seawater, which is a good
tool in estimating the mean strength of polyanion interaction in seawater,
was applied. The comparison of experimental and estimated results showed t
hat a suitable complexation model can be used with reasonable accuracy to p
redict acid-base properties of carboxylic ligands in seawater. (C) 1999 Els
evier Science B.V. All rights reserved.