Abstract
The purpose of this study is to reveal the role of cupric ions as a natural water contaminant in the H 2O 2/UV oxidation of humic acids. Humic acids are naturally occurring organic matter and exhibit a strong tendency of complexation with some transition metal ions. Chlorination of humic acids causes potential health hazards due to formation of trihalomethane (THM). The removal of THM precursors has become an issue of public concern. The H 2O 2/UV process is capable of mineralizing humic acids due to formation of a strong oxidant, hydroxyl radicals, in reaction solution. Experiments were conducted in a re-circulated photoreactor. Different cupric concentrations (0–3.8 mg/l) and different pH values (4–9) were controlled to determine their effects on the degradation of humic acids, UV light absorbance at 254 nm, and H 2O 2. The presence of cupric ions inhibits humic mineralization and decreases the rate of destruction of humic acids which absorb UV light at 254 nm. On the other hand, the higher the cupric concentration, the lower the H 2O 2 decomposition rate. In the studied pH range, the minimum of total organic carbon (TOC) removal occurs at pH=6 in the presence of 2.6 mg/l of cupric ions; both acidification (pH=4) and alkaline condition (pH=9) lead to a better removal of TOC. It is inferred from this study that the cupric-complexed form of humic acids is more refractory than the non-complexed one.
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