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Updated: Jul 8, 2025

Characterizing Lewis Pairs Using Titration Coupled with In Situ Infrared Spectroscopy
Published on: February 20, 2020
Determination of the pKa Value of Protonated Mono and Polyamine in Solution Using Fourier Transform Infrared
Martin Müller1,2, Luise Wirth1,2, Birgit Urban1
1Department Functional Colloidal Materials, Leibniz-Institut für Polymerforschung Dresden e.V., Dresden, Germany.
Abstract:
The pKa values of propanolamine hydrochloride (PAMH) and poly(allylamine hydrochloride) (PAAMH) in concentrated solutions were determined by both Fourier transform infrared spectroscopy (FT-IR) titration and classical potentiometric (POT) titration and compared. Starting with the respective fully protonated forms PAMH and PAAMH and increasing the pH value by sodium hydroxide addition in situ attenuated total reflection FT-IR (ATR FT-IR) spectra on PAMH and PAAMH solutions show the variation of diagnostic infrared (IR) bands. From the decrease of the most intense δ(NH3+) band the dissociation process of the NH3+ groups could be followed. Thereby, from the respective normalized band area A the dissociation degree αIR of the ammonium groups could be determined. Plotting pH versus αIR and fitting this curve by a modified Henderson-Hasselbalch function pH = pKa + B log (αIR/1 - αIR) the parameters pKa and cooperativity factor B were obtained. pKa values from FT-IR titration were qualitatively in line with respective pKa values from POT titration. Quantitative systematic pKa deviations between polyelectrolyte (PEL) and respective monoelectrolyte and the tentative effects of PEL molecular weight, ambient ionic strength, and titration concept (FT-IR and POT) are discussed based on classical models of weak PEL.
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