Influence of the physical and chemical properties of soil on the retention process of isoxaflutole and its two main derivatives

被引:14
作者
Beltran, E
Fenet, H
Cooper, JF
Coste, CM
机构
[1] CNRS, Ctr Phytopharm, UMR 5054, F-66860 Perpignan, France
[2] Fac Pharm Montpellier, Chim Analyt Lab, Montpellier 5, France
关键词
adsorption; desorption; chemical degradation; organic matter content;
D O I
10.1046/j.1365-3180.2002.00299.x
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Isoxaflutole is a new pre-emergence herbicide for use in maize and sugarcane. Its two main derivatives are a diketonitrile derivative, the 2-cyano-3-cyclopropyl-1-(2-methanesulfonyl-4-trifluoromethylphenyl)propan-1,3-dione, named DKN, and a benzoic acid derivative, the 2-methanesulfonyl-4-trifluoromethylbenzoic acid, named BA. The adsorption/desorption processes have never been studied for isoxaflutole (IFT) at high concentrations nor for BA, and the present work aimed at completing the knowledge of the behaviour of these three molecules in conditions close to those encountered in the context of agricultural use. The adsorption/desorption study was conducted on seven soils of different physical and chemical properties, using the batch equilibrium technique. During the experiments, IFT was chemically converted into DKN in a continuous manner. This reaction appeared to be dependent on the pH of the soil and was taken into account in the calculations of the adsorbed and desorbed amounts. The adsorption isotherms obtained were predominantly C-shaped for IFT and DKN and S-shaped for BA, but some differences appeared on a few soils. They fitted well the Freundlich equation, and the values of the Freundlich coefficient K-fa showed that, whatever the soil, IFT was more adsorbed than its two derivatives. The main parameter influencing the adsorption of IFT appeared to be the organic matter content, whereas this effect was not evident for DKN and BA. No correlation was found between the extent of adsorption and either clay content or pH of the soil, for the three molecules.
引用
收藏
页码:385 / 393
页数:9
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