In-situ characterization of dissolved organic matter removal by coagulation using differential UV–Visible absorbance spectroscopy

Abstract Removing dissolved organic matter (DOM) is of great concern due to its adverse effects on water supplies. Great effort has been given to studying DOM removal by coagulation, while the mechanism of DOM removal and the changes in its properties during coagulation have not been clearly illustrated due to the limitations of detection methods under practical environmental conditions. In this paper, the changes in DOM during coagulation were quantified using differential UV–Visible absorbance spectroscopy, and the differential spectra of DOM in the wavelength range of 200–600 nm could be deconvoluted into six Gaussian bands with maxima at approximately 200, 240, 276, 316, 385, and 457 nm after coagulation, respectively. The intensity of these maxima decreased with the type and dosage of coagulants. These observations should reflect the difference in the removability of DOM by coagulation, and this perspective was further confirmed by examining the deprotonation-protonation properties of DOM before and after coagulation. The affinity sites of DOM in coagulated waters, quantified by spectra parameter DlnA400 (differential log-transformed spectra at wavelength 400 nm) in combination with the revised NICA model, increased as the coagulant dosage, which indicates that coagulation is inclined to remove the DOM fraction with fewer functional groups. Polyaluminum chloride (PAC) and Al-aggregate (Al13) were more efficient than Alum for removing DOM due to their high efficiency for removing DOM fractions with fewer functional groups. The residual dissolved Al concentration depended on the total amount of reactive binding sites in DOM, and there was a strong linear correlation between residual dissolved Al and the total amount of reactive binding sites in DOM for Alum, while a weaker correlation was presented for PAC and Al13. This indicates that Ala was the dominant species to bind with the affinity sites in DOM to form residual dissolved Al.