Adsorption of diclofenac on activated carbon and its hypochlorination in the presence of dissolved organic matter

The nonsteroidal anti-inflammatory drug “diclofenac” is the pharmaceutically active ingredient of several medicines. Since the compound is used in many of its water-soluble salt forms, it is one of the most frequently found pollutants in different parts of the water cycle. Its reaction with sodium hypochlorite was investigated in the presence of humic substances and sandy soil extract at neutral pH at 25 and 250 mg/L initial concentrations. In the lower concentration, the reaction follows a pseudo-first-order kinetics, while at the higher concentration, it is described as the sum of two first-order reactions. These kinetic results, together with the organic chlorine content of the residues, indicated that both chlorination and oxidation took place. The chlorination is significantly faster. The colloids present catalyze the reactions: The clay minerals of soil extract accelerated the chlorination, while the humic acids could work as photocatalysts in the oxidation, while these compounds themselves were chlorinated. The adsorption of diclofenac on activated carbon was enhanced by humic substances, and every isotherm had a breaking point near to 3 mg/L equilibrium concentration (c _e) resulting in two steps. According to the measurements of the zeta potential, the system proved to be relatively stable at this c _e value, but at higher diclofenac concentrations the stability retained only in the presence of the hydrophilic fulvic acid. The results supported the adsorption hypothesis that in the first step the charge transfer interaction while in the second step hydrogen bond formation plays the key role.