Synergistic removal of ammonium by monochloramine photolysis

Abstract

The presence of ammonium (NH4+) in drinking water treatment results in inhibition of disinfection efficiency and formation of nitrogenous disinfection by-products. Our previous study found monochloramine (NH2Cl) photolysis under 254 nm UV irradiation can be effective for removal of NH4+; however, the mechanisms of NH4+ degradation in this process were unknown. The kinetics and fundamental radical chemistry responsible for NH4+ removal in the UV/NH2Cl process were investigated in this study. The results showed that the pseudo first-order rate constant for NH4+ degradation in the UV/NH2Cl process ranged between 3.6 × 10-4 to 1.8 × 10-3 s-1. Solution pH affected radical conversion and a higher NH4+ degradation efficiency was achieved under acidic conditions. The effects of chloride were limited; however, the presence of either bicarbonate or natural organic matter scavenged radicals and inhibited NH4+ removal. NH2Cl photolysis generated an aminyl radical (NH2•) and a chlorine radical (Cl•) that further transformed to a chlorine dimer (Cl2•-) and a hydroxyl radical (HO•). The second-order rate constants for Cl• and Cl2•- reacting with NH4+ were estimated as 2.59 × 108 M-1s-1 and 3.45 × 105 M-1s-1 at pH 3.9, respectively. Cl•, Cl2•-, and HO• contributed 95.2%, 3.5%, and 1.3% to NH4+ removal, respectively, at the condition of 3 mM NH2Cl and pH 7.5. Major products included nitrite and nitrate, possibly accompanied by nitrogen-containing gases. This investigation provides insight into the photochemistry of NH4+ degradation in the UV/NH2Cl process and offers an alternative method for drinking water production.