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Interactions of two sulfonylurea herbicides with organoclays

Published online by Cambridge University Press:  01 January 2024

Maria Jose Carrizosa ,
Maria del Carmen Hermosin ,
William C. Koskinen  and
Juan Cornejo
Maria Jose Carrizosa
Affiliation:
USDA-ARS, Soil and Water Management Research Unit, 1991 Upper Buford Cir. Rm 439, St. Paul, MN 55108, USA
Maria del Carmen Hermosin
Affiliation:
Instituto de Recursos Naturales y Agrobiologia de Sevilla, CSIC, P.O. Box 1052, 41080 Sevilla, Spain
William C. Koskinen*
Affiliation:
USDA-ARS, Soil and Water Management Research Unit, 1991 Upper Buford Cir. Rm 439, St. Paul, MN 55108, USA
Juan Cornejo
Affiliation:
Instituto de Recursos Naturales y Agrobiologia de Sevilla, CSIC, P.O. Box 1052, 41080 Sevilla, Spain
*
*E-mail address of corresponding author: [email protected]
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Abstract

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The sorption of two sulfonylurea herbicides (SU), metsulfuron methyl and nicosulfuron, on pure clays and organoclays was investigated. Three clays (Arizona smectite, SAz-1, Wyoming smectite, SWy-2, and hectorite, SHCa-1), were treated with amounts of octadecylammonium (ODA) or dioctadecyldimethylammonium (DODMA) cations equal to ∼50 and 100% of the clays’ cation exchange capacity (CEC). Sorption isotherms were fitted to the Freundlich equation. While no measurable sorption was found on the pure clays (Kf = 0), organoclays prepared using both primary and quaternary amines were effective as SU sorbents. The metsulfuron methyl Kf values ranged between 196 and 1498 µmol1−1/n kg−1 L1/n, and Kf values for nicosulfuron, which were lower than those of metsulfuron methyl, ranged from 35 to 198 umol1−1/n kg−1 L1/n. As shown by sorption coefficients, Kd and KOC, SWy-2 treated with DODMA at ∼100% of the CEC was the most effective sorbent for metsulfuron, Kd = 684 L kg−1 and KOC = 2138 L kg−1. For nicosulfuron the most effective sorbent was SAz-1 with ODA at ∼ 50% of the CEC (Kd = 147 L kg−1 and KOC = 1233 L kg−1). In contrast to other weak-acid herbicides, such as phenoxy and picolinic acids, no clear relationships were found between sorption and layer charge, organic carbon content, and basal spacing of the organoclays for both sulfonylurea herbicides. Sorption of both herbicides on organoclays was assumed to involve hydrophobic and polar interactions for which the availability of interlayer room between organocations was a very important factor.

Keywords

MetsulfuronNicosulfuronOrganoclaysSorptionSulfonylureas
Type
Research Article
Information
Clays and Clay Minerals , Volume 52 , Issue 5 , October 2004 , pp. 643 - 649
Copyright
Copyright © 2004, The Clay Minerals Society

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