E S I L V A . Can. J. Chem. 58, 547 (1980). A model system composed of bentonite, humic acid (HA), polystyrene sulphonic acid (PSSA), methylene blue (MB), and paraquat was used to characterize the possible interactions of organocations in natural waters. The adsorption and desorption studies with bentonite indicated that the clay had a strong preference for the organocations over alkali and alkaline earth cations. Paraquat saturated the bentonite up to the cation exchange capacity whereas methylene blue did not completely saturate the clay but did form methy!ene blue aggregates on the clay surface. The aggregates could be readily removed by washing with distilled water. The organocation interactions with the anionic polyelectrolytes were more susceptible to changes in pH or ionic strength. Paraquat could be completely desorbed from HA and PSSA by raising the solution ionic strength to 0.1. Methyiene blue could not be completely removed from the humic acid bat could be removed from PSSA by raising the ionic strength to 0.1. The studies indicate that a combination of dialysis separations. variation of ionic strength, and spectrophotometric analysis could be used to determine the free paraquat and the bound paraquat susceptible to changes in environmental levels of pH and ionic strength. Can. J. Chem. 58,547 (1980) Nous avons utilise un systeme compose de bentonite, d'acide humique (AH), d'acide polystyrene sulfonique (APSS), de bleu de methylene (BM) et de paraquat afin de caracteriser les interactions possibles des organocations dans les eaux naturelles. Les Ctudes d'adsorption et de desorption avec la bentonite indiquent que I'argile prefere de beaucoup les organocations aux cations des terres alcalines. Le paraquat sature la bentonite jusqu'a la capacite d'ichange des cations alors que le bleu de methylene ne le sature pas completement mais forme des agregats de bleu de methylene Bla surface de I'argile. Les agregats peuvent itre faciiement enlevis par lavage B I'eau distillee. Les interactions entre les organocations et les polyelectrolytes anioniques sont plus susceptibles de varier selon la force ionique ou le pH. Le paraquat peut itre completement desorbe du AM ou du APSS en augmentant la force ionique de la solution a 0.1. Le bleu de methylene ne peut Ctre enleve completement de l'acide humique; dans le cas du AQSS on peut toutefois I'enlever en augmentant la force ionique aO.l. Les etudes indiquent qu'onpeut utiliserune combinaison de separation par dialyse, de variation de la force ionique et d'analyse spectrophotometrique, pour determiner le paraquat sous forme libre ou combinee susceptible de changer dans des milieux de differents pH ou de force ionique.[Traduit par le journal] Introduction soluble, colloidal, and particulate species plays a ~h~ interactions of organic compounds vital role in the toxicity of organic herbicides. Gilin the environment play an important role in the lott et al. (1) have shown that the presence of seditransport and persistence of the chemicals. The ment in test systems si...
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