2000
DOI: 10.4141/s99-071
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Kinetics and equilibria of Metribuzin sorption on model soil components

Abstract: Sha'ato, R., Buncel, E., Gamble, D. G. and vanLoon, G. W. 2000. Kinetics and equilibria of Metribuzin sorption on model soil components. Can. J. Soil Sci. 80: 301-307. Sorption to solid phase materials is known to significantly affect the transport, bioavailability and ultimate fate of organic contaminants in soils and sediments. In order to develop a complete description of the fate of these compounds, it is necessary to understand both equilibrium interactions and rates and mechanisms of the sorption process… Show more

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Cited by 21 publications
(15 citation statements)
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“…Nevertheless, triazines are readily adsorbed on montmorillonites saturated with Ca 27. On the other hand, the affinity of metribuzin is notably lower on kaolinite than on montmorillonite 28. Thus, metribuzin sorption on P44, LM and TM soils is related to the content and type of clay mineral present in the soil (Table 2).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Nevertheless, triazines are readily adsorbed on montmorillonites saturated with Ca 27. On the other hand, the affinity of metribuzin is notably lower on kaolinite than on montmorillonite 28. Thus, metribuzin sorption on P44, LM and TM soils is related to the content and type of clay mineral present in the soil (Table 2).…”
Section: Resultsmentioning
confidence: 99%
“…The highest adsorption of metribuzin was observed on LM soil. This herbicide shows larger sorption kinetics and higher affinity for amorphous oxides of iron and aluminium than clay minerals, even when the latter are saturated with monovalent cations 28. Therefore, the high content of iron and aluminium oxides in LM soil could be responsible for the high metribuzin sorption.…”
Section: Resultsmentioning
confidence: 99%
“…Even in many cases, these compounds have replaced organochlorine pesticides 1–3. Nevertheless, exposure to excess levels of such compounds is very dangerous not only because of human damage (exerts delayed cholinergic toxicity) but also due to environment toxicity 4–11.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4] The reaction of the broad spectrum insecticide fenitrothion, 1, with a variety of oxygen-based nucleophiles has engaged our recent attention. 3,4 In aqueous solution, 1 reacts with a variety of oxygen nucleophiles, to include some alpha-nucleophiles and a series of structurally related phenoxides as well as the highly basic nucleophiles OH -and CF 3 CH 2 O -, exclusively at the P center.…”
Section: Introductionmentioning
confidence: 99%