Author(s)

Jörgen Rosenqvist, Caroline M. Jonsson

Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, Sweden.

The dissociation behavior of two dihydroxybenzoic acid isomers, 2,3-DHBA and 3,4-DHBA, at 281 K and 293 K was determined by potentiometric titrations in 0.01 M NaCl and 0.03 M NaCl. Results showed that the dissociation enthalpy for the carboxylic group in DHBA is close to zero, resulting in dissociation constants that do not vary appreciably with temperature, whereas the dissociation constants for the first hydroxyl group vary significantly with temperature. Increasing ionic strength was found to result in increased values for the second dissociation constant, whereas the effect on the first dissociation constant was less clear.

2, 3-Dihydroxybenzoic Acid, 3, 4-Dihydroxybenzoic Acid, Dissociation Constant, pKa, Temperature, Ionic Strength, Surface Water

Rosenqvist, J. and Jonsson, C. (2017) Potentiometric Study of Dissociation Constants of Dihydroxybenzoic Acids at Reduced Ionic Strengths and Temperatures. American Journal of Analytical Chemistry, 8, 142-150. doi: 10.4236/ajac.2017.82011.