Almtraet --The adsorption of the herbicide imazamethabenz-methyl, a mixture of the two isomers methyl (_+)-2-[4,5-dihydro-4-methyl-4-(1 -methylethyl)-5-oxo-1H-imidazol-2-yl]-4-methylbenzoate (para isomer) and methyl (+_)-2-[4,5-dihydro-4-methyl-4-(1 -methylethyl)-5-oxo-1H-imidazol-2-yl]-5-methylbenzoate (meta isomer), from water onto AP +-, Fe 3+-, Ca 2+ -, K +-and Na+-montmorillonite was studied by analytical (HPLC) methods. The adsorption from an organic solvent was also investigated by spectroscopic (IR) and X-ray diffraction measurements. It was observed that, depending on the acidic properties of the exchangeable cations, two different mechanisms may take #ace. The first one, acting on Fe a+-and AI a+-clays, involves the protonation of the more basic nitrogen atom ofimidazolinone ring of the herbicide because of a proton transfer from the acidic metal-bound water, followed by adsorption on the clay surfaces. In this case, the clay surfaces have greater affinity for the meta than the para isomer, due to the extra-stabilization of the meta protonated form by resonance. The second mechanism, taking place on Ca 2 § -, K +-and Na +-clays, is hydrogen-bond formation between the ester carbonyl group of the herbicide and hydration water metal ions and is not affected by the structure of the isomers.