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Journal of Environmental Quality 32:949-956 (2003)
© 2003 American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America

TECHNICAL REPORTS
Organic Compounds in the Environment

Soil Sorption of Acidic Pesticides

Modeling pH Effects

Claudio A. Spadotto* and Arthur G. Hornsby

Soil and Water Science Dep., Univ. of Florida

* Corresponding author (spadotto{at}cnpma.embrapa.br)

Received for publication December 18, 2000. A model of acidic pesticide sorption in soils was developed from theoretical modeling and experimental data, which initially considered a combination of a strongly acidic pesticide and a variable-charge soil with high clay content. Contribution of 2,4-D [(2,4-dichlorophenoxy) acetic acid] anionic-form sorption was small when compared with molecular sorption. Dissociation of 2,4-D was not sufficient to explain the variation in Kd as a function of pH. Accessibility of soil organic functional groups able to interact with the pesticide (conformational changes) as a function of organic matter dissociation was proposed to explain the observed differences in sorption. Experimental 2,4-D sorption data and Koc values from literature for flumetsulam [N-(2,6-difluorophenyl)-5-methyl [1,2,4] triazolo [1,5-a] pyrimidine-2-sulfonamide] and sulfentrazone [N-[2,4-dichloro-5-[4-(difluromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-y1] phenyl] methanesulfonamide] in several soils fit the model.


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JEQ 2003 32: 745-750. [Full Text]  



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J. Gaultier, A. Farenhorst, J. Cathcart, and T. Goddard
Regional Assessment of Herbicide Sorption and Degradation in Two Sampling Years
J. Environ. Qual., August 8, 2008; 37(5): 1825 - 1836.
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