Summary. Dispersive liquid-liquid microextraction in combination with an in situ derivatization is suggested for parabens sampling and preconcentration. The derivatization was carried out with acetic anhydride under alkaline conditions maintained using dipotassium hydrogen phosphate. The effects of an extraction solvent type, extraction and disperser solvents volume, extraction time, and ionic strength of the solution on the extraction efficiency were investigated. Chlorobenzene containing n-hexadecane as internal standard was used as an extracting solvent and acetone was used as a disperser solvent. The calibration graphs were linear up to 10 mg mL −1 , correlation coefficients were 0.997-0.999, enrichment factors were from 70 for methylparaben to 210 for butylparaben, and detection limits were 22, 4.2, 3.3, and 2.5 μg L −1 for methylparaben, ethylparaben, propylparaben, and butylparaben, respectively. Repeatabilities of the results were acceptable with relative standard deviations up to 11%. A possibility to apply the proposed method for parabens determination in water samples was demonstrated.

Dispersive liquid-liquid microextraction in combination with an in situ derivatization is suggested for methyltin compound sampling and preconcentration from water solutions. The derivatization was carried out with sodium tetraethylborate at pH 3. The effects of extraction and disperser solvents type, volume, and extraction time on the extraction efficiency were investigated. 1,2-Dichlorobenzene was used as an extraction solvent and ethanol was used as a disperser solvent. The calibration graphs for all the analytes were linear up to 2 μg (Sn) L(-1), correlation coefficients were 0.998-0.999, LODs were 0.13, 0.05, and 0.06 ng (Sn) L(-1) for trimethyltin, DMT, and monomethyltin, respectively. Repeatabilities of the results were acceptable with RSDs up to 12.1%. A possibility to apply the proposed method for methyltin compound determination in water samples was demonstrated.