Aqueous ozone solutions for pesticide removal from potatoes.

The presence of pesticide residues in potatoes is of concern because of the potential impact to human health due to the high consumption of this vegetable. In this study, aqueous solutions with and without ozone saturation as postharvest wash treatment at pH 4.0, 7.0, and 9.0 were tested to remove chlorothalonil from potatoes. The method used for pesticide analysis has been validated, presenting recovery values of 94-103%, with variations in the repeatability coefficients of ≤10.6%, and a quantification limit of 0.05 mg kg-1 Regardless of pH, treatment with aqueous ozone solutions removed 70-76% of the pesticide present in the potato. In the no-ozone treatments, the percentage average removal of chlorothalonil residues in potatoes was only 36%. Over 24 days of storage, the quality of potatoes washed with aqueous ozone solutions was not significantly different from those washed with pure water.

Mobility and persistence of the herbicide fomesafen in soils cultivated with bean plants using SLE/LTP and HPLC/DAD.

A method has been optimized and validated for the determination of fomesafen in soils using solid-liquid extraction with low-temperature partitioning (SLE/LTP) and analysis by liquid chromatography with a high-efficiency diode array detector (HPLC/DAD). The method was used to evaluate the persistence and mobility of this herbicide in different soils cultivated with bean plants. Recovery values were ≥98.9 %, with variations in the repeatability coefficients of ≤15 %, and a detection limit of 7.3 µg kg(-1). Half-life values of fomesafen were between 60 and 71 days in soil cultivated using a no-till system and 99 and 114 days in soil cultivated using a conventional tillage system. The mobility of fomesafen was moderate and mainly influenced by the organic matter content, pH, and soil type. In Red-Yellow Argisol, which has a higher content of organic matter, the leaching of fomesafen was less pronounced. In Red-Yellow Latosol, which has smaller amounts of organic matter and high pH, the leaching of fomesafen was more pronounced.

Direct introduction of water sample in multisegmented flow-injection analysis for sulfide determination.

The present paper describes an inline flow-injection analysis system for the determination of sulfide in water samples, exploiting the Fischer reaction. Water samples were collected and introduced into a reactor of the FIA system. The sulfide released, after sample acidification, was carried out with a nitrogen gas flow and mixed with N,N diethyl-p-phenylenediamine (DEPD) solution in the presence of Fe(III). The blue dye formed was measured in the wavelength range between 672-679 nm. An evaluation of the effects of chemical and flow factors was performed using the factorial design of two levels, while optimization was accomplished by a Doehlert matrix. The system presented two linear-response ranges: the first of 0.433 to 400 µg L(-1) and the second of 400 to 3500 µg L(-1). The detection and quantification limit were found to be 0.130 and 0.433 µg L(-1), respectively, while the sample throughput was 12 h(-1). The precision was evaluated as the relative standard deviation (n = 10); for 50 and 100 µg L(-1) sulfide it was found to be 1.9 and 2.3%, respectively. The method showed satisfactory selectivity regarding the main interference present in environmental samples. The accuracy of the method was successfully evaluated in environmental water samples after a comparison with a literature reference method.