| Autor: |
Ha B; a Department of Chemistry , Jess and Mildred Fisher College of Science and Mathematics, Towson University , Towson , Maryland , USA., Zamini L; a Department of Chemistry , Jess and Mildred Fisher College of Science and Mathematics, Towson University , Towson , Maryland , USA., Monn J; b Center for Geographic Information Systems, Towson University , Towson , Maryland , USA., Njoroge S; c Department of Chemistry , Kenyatta University , Nairobi , Kenya., Thimo L; c Department of Chemistry , Kenyatta University , Nairobi , Kenya., Ondeti M; c Department of Chemistry , Kenyatta University , Nairobi , Kenya., Murungi JI; c Department of Chemistry , Kenyatta University , Nairobi , Kenya., Muhoro CN; a Department of Chemistry , Jess and Mildred Fisher College of Science and Mathematics, Towson University , Towson , Maryland , USA. |
| Abstrakt: |
Water quality assessment was conducted on the Ruiru River, a tributary of an important tropical river system in Kenya, to determine baseline river conditions for studies on the aquatic fate of N-methyl carbamate (NMC) pesticides. Measurements were taken at the end of the long rainy season in early June 2013. Concentrations of copper (0.21-1.51 ppm), nitrates (2.28-4.89 ppm) and phosphates (0.01-0.50 ppm) were detected at higher values than in uncontaminated waters, and attributed to surface runoff from agricultural activity in the surrounding area. Concentrations of dissolved oxygen (8-10 ppm), ammonia (0.02-0.22 ppm) and phenols (0.19-0.83 ppm) were found to lie within normal ranges. The Ruiru River was found to be slightly basic (pH 7.08-7.70) with a temperature of 17.8-21.2°C. The half-life values for hydrolysis of three NMC pesticides (carbofuran, carbaryl and propoxur) used in the area were measured under laboratory conditions, revealing that rates of decay were influenced by the electronic nature of the NMCs. The hydrolysis half-lives at pH 9 and 18°C decreased in the order carbofuran (57.8 h) > propoxur (38.5 h) > carbaryl (19.3 h). In general, a decrease in the electron density of the NMC aromatic ring increases the acidity of the N-bound proton removed in the rate-limiting step of the hydrolysis mechanism. Our results are consistent with this prediction, and the most electron-poor NMC (carbaryl) hydrolyzed fastest, while the most electron-rich NMC (carbofuran) hydrolyzed slowest. Results from this study should provide baseline data for future studies on NMC pesticide chemical fate in the Ruiru River and similar tropical water systems. |
