Laboratório de Resíduos e Contaminantes-Embrapa Meio Ambiente, Jaguariúna, SP, Brazil.
J Environ Sci Health B. 2010 Jan;45(1):89-94. doi: 10.1080/03601230903404598.
Several different Advanced Oxidation Processes (AOPs) including ozonation at pH 6.5 and 10, photolysis and heterogeneous photocatalysis using TiO(2) as semiconductor and dissolved oxygen as electron acceptor were applied to study the degradation of glyphosate (N-phosphonomethyl glycine) in water. The degree of glyphosate degradation, the reactions kinetic and the formation of the major metabolite, aminomethyl phosphonic acid (AMPA), were evaluated. Ozonation at pH 10 resulted in the maximum mineralization of glyphosate. It was observed that under the experimental conditions used in this study the degradation of glyphosate followed the first-order kinetics. The half-life obtained for glyphosate degradation in the O(3)/pH 10 process was 1.8 minutes.
几种不同的高级氧化工艺(AOPs),包括 pH 值为 6.5 和 10 的臭氧氧化、光解和使用 TiO(2) 作为半导体和溶解氧作为电子受体的多相光催化,都被应用于研究水中草甘膦(N-膦酰甲基甘氨酸)的降解。评估了草甘膦的降解程度、反应动力学和主要代谢物氨甲基膦酸(AMPA)的形成。在 pH 值为 10 的臭氧氧化作用下,草甘膦的矿化程度达到最大。研究结果表明,在本研究中使用的实验条件下,草甘膦的降解遵循一级动力学。在 O(3)/pH 10 工艺中,草甘膦降解的半衰期为 1.8 分钟。