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Updated: Jul 13, 2026

Quantification of Humic and Fulvic Acids in Humate Ores, DOC, Humified Materials and Humic Substance-Containing Commercial Products
Published on: March 18, 2022
Characterization of noncovalent interactions between 6-propionyl-2-dimethylaminonaphthalene (PRODAN) and dissolved
Praveen Gadad1, Hongxia Lei, Mark A Nanny
1School of Civil Engineering and Environmental Science, College of Engineering, The University of Oklahoma, Norman 73019, USA.
Abstract:
Noncovalent interactions between the fluorescent probe 6-propionyl-2-dimethylaminonaphthalene (PRODAN) and dissolved Norman Landfill leachate fulvic acid, Suwannee River fulvic acid, Suwannee River humic acid, and Leonardite humic acid were examined as a function of pH, fulvic and humic acid (FA and HA) concentration, and solvent polarity using steady-state fluorescence spectroscopy. Static quenching processes, as indicated by linear Stern-Volmer plots and high K(d) values, were positively correlated with the % aromaticity of the FA and HAs, as well as with solution pH. Results illustrate that for FA molecules with relatively low % aromaticity values, solvophobic interactions between PRODAN and FA are the primary interaction mode. For HA molecules with higher % aromaticity, PRODAN engages in both solvophobic interactions and pi-pi interactions, in particular electron donor-acceptor interactions, via condensed aromatic, electron-accepting moieties inherent within HA molecules. Experiments modifying solvent polarity demonstrated that protonation of carboxylic acid functional groups at low pH ( approximately 4) increased the hydrophobicity of the dissolved FA and HA molecules, thereby enhancing noncovalent interactions with PRODAN through increased solvophobic forces.
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