Journal
ENVIRONMENTAL SCIENCE-WATER RESEARCH & TECHNOLOGY
Volume 5, Issue 5, Pages 897-909Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ew00714d
Keywords
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Funding
- University of Minnesota
- NSF Sustainability Research Networks [1444745]
- Environment and Natural Resources Trust Fund
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The first step of an anaerobic ammonia oxidation (anammox) system is typically the formation of nitrite (NO2-) via partial nitritation, which can generate hydroxyl radical (OH) when irradiated with ultraviolet (UV) light. This study demonstrated that the presence of nitrite in buffer and wastewater matrices during medium-pressure UV irradiation (at lambda >= 220 or >= 280 nm) enhanced the degradation of select pharmaceutical compounds of different therapeutic classes (atenolol, carbamazepine, fluoxetine, and trimethoprim). Total pharmaceutical removals in a wastewater matrix irradiated at lambda >= 280 for 120 minutes were 47% for trimethoprim, 50% for carbamazepine, 60% for atenolol, and 57% for fluoxetine at fluences of 58.6 mEi m(-2) (2033.1 mJ cm(-2)). When irradiated at lambda >= 220 for 60 minutes, removals were 52% for trimethoprim, 56% for carbamazepine, 69% for atenolol, and 90% for fluoxetine at fluences of 634.7 mEi m(-2) (23 969.2 mJ cm(-2)). Reaction with OH accounted for similar to 78-90% of pharmaceutical removal at lambda >= 280 nm. Although direct photolysis did contribute to target compound removal for irradiation with lambda >= 220 nm, much of the light was absorbed in the buffer and wastewater matrices, and reaction with OH accounted for similar to 70-93% of pharmaceutical removal. Quencher experiments with isopropanol confirmed the importance of reaction with OH as the main contributor to pharmaceutical removal. para-Chlorobenzoic acid was used as a probe to estimate steady-state OH concentrations, which averaged 8.58 x 10(-15) M for both matrices at lambda >= 280 nm and 3.50 x 10(-14) M for both matrices at lambda >= 220 nm. Nitrosamines were formed and accumulated during the UV treatment step, however, concomitant with their direct photochemical destruction. Presence of the pharmaceutical micro-pollutants studied, such as the secondary-amine containing atenolol and fluoxetine, did not elevate nitrosamine formation.
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