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  • Degradation of bromoxynil and trifluralin in natural water by direct photolysis and UV plus H(2)O(2) advanced oxidation process.

Degradation of bromoxynil and trifluralin in natural water by direct photolysis and UV plus H(2)O(2) advanced oxidation process.

Water research (2010-02-02)
Pamela Chelme-Ayala, Mohamed Gamal El-Din, Daniel W Smith
ABSTRACT

The degradation of two pesticides, bromoxynil and trifluralin, was investigated in ultrapure and natural water solutions under ultraviolet (UV) light and a combination of UV and hydrogen peroxide (H(2)O(2)). The effect of pH on the photooxidation of the pesticides was also studied. The results indicated that under direct photolysis with monochromatic light at 253.7 nm and different conditions, the photochemical rates followed first-order kinetics, with fluence-based rate constants ranging from 9.15 x 10(-4) to 6.37 x 10(-3) cm(2) mJ(-1) and 7.63 x 10(-3) to 1.47 x 10(-2) cm(2) mJ(-1) for bromoxynil and trifluralin, respectively. Quantum yields, in the range of 0.08-0.25 for bromoxynil and 0.12-0.72 for trifluralin, were observed in experiments using ultrapure water. The study also found that the UV/H(2)O(2) process enhanced the oxidation rate in comparison to direct photolysis. A 90% degradation with UV dose of 333 and 188 mJ cm(-2) was achieved for bromoxynil and trifluralin, respectively, in natural water, in presence of 8.8 x 10(-4) M H(2)O(2). To assess the aquatic toxicity, the Microtox 81.9% screening test protocol was used before and after treatment. The test results indicated a decrease in the acute toxicity of the samples after treatment for both pesticides.

MATERIALS
Product Number
Brand
Product Description

Supelco
Trifluralin, PESTANAL®, analytical standard
Supelco
Bromoxynil, PESTANAL®, analytical standard
Supelco
Trifluralin solution, 100 μg/mL in acetonitrile, PESTANAL®, analytical standard