Interactions of Chlorine with Natural Organic Matter and Formation of Intermediates: Evidence by Differential Spectroscopy

This communication describes the use of differential absorbance spectroscopy to explore the intermediates formed during halogenation of natural organic matter (NOM). The differential spectra of chlorinated NOM comprise two contributions. The primary component is negative and has a peak near 270 nm. The shape of this band is independent of chlorine dose, and its intensity increases monotonically with Cl₂ dose. The second component is positive, with a well‐defined peak near 280 nm and another, broader band in the 340...380 nm range. The second component is noticeable at low chlorine concentrations but disappears with increasing Cl₂ dose. We attribute this component to aromatic chlorinated intermediates formed prior to the release of identifiable smaller species such as haloacetic acids. We believe that this component of the differential spectra can be used to probe the identity, formation and breakdown of the halogenated intermediates.