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Ramón Batlle

Publications and source records attributed to Ramón Batlle.

4 recordsLinked to original sources

Subcritical water and dynamic sonication-assisted solvent extraction of fluorescent whitening agents and azo dyes in paper samples.

Two low-volume solvent continuous extraction methods are applied to the extraction of paper matrices. In the methods reported here, a complex mixture of fluorescent whitening agents (FWAs) and azo dyes (AZOs) used in paper materials intended to come into contact with foodstuffs was extracted by using subcritical water extraction (SWE) and dynamic sonication-assisted solvent extraction (DSASE). Rationale for the work is based upon migration concerns of these groups of analytes from the packaging to the packaged items, thus compromising their subjective and/or objective quality. In SWE, sample was extracted in 21 min with 0.5 mL of water, whereas the DSASE method required 11 min and used 7 mL of water. DSASE was further developed by incorporating an organic modifier in order to change water polarity, thus improving extraction of moderately polar analytes. This way, modified-DSASE used a total organic volume of 0.9 mL which represents a reduction of 200 times in organic solvent consumption (200 mL versus approximately 1.0 mL) and 11 times in extraction time (2h versus 11 min) compared to the existing methods. SWE was able to extract only 9 out of 12 test analytes with average recoveries between 10 and 25% whereas modified-DSASE succeed in extracting all the target analytes with an average recovery of 89%. Complete discussion and explanation concerning these differences are provided in the text.

Azo Compounds↗

Application of single-drop microextraction to the determination of dialkyl phthalate esters in food simulants.

A fast and simple method, using static single-drop microextraction (SDME), has been developed to facilitate the identification and quantification of seven dialkyl phthalate esters in the three aqueous food simulants. The simulants were: A, distilled water; B, 3% (w/v) acetic acid/water; and C, 15% (v/v) ethanol/water. The extraction is performed by simply suspending a drop of organic solvent in the aqueous sample using a conventional gas chromatography (GC) microsyringe. Following extraction, the organic phase is withdrawn into the syringe and analyzed by gas chromatography and flame ionization detection (FID). The optimized method yields a linear calibration curve over three orders of magnitude for all the simulants, and method detection limits (MDLs) allowing detection of all the studied compounds at concentrations below migration limits established by the European Union. The accuracy of the SDME method was tested and compared to that of solid-phase microextraction (SPME) by recovery experiments using spiked samples, with results ranging from 85 to 115% in most cases.

Food Analysis↗

Enhanced detection of nitroaromatic explosive vapors combining solid-phase extraction-air sampling, supercritical fluid extraction, and large-volume injection-GC.

A complete method for sampling and analyzing of energetic compounds in the atmosphere is described. The method consists of the hyphenation of several techniques: active air sampling using a solid-phase extraction cartridge to collect the analytes, extraction of the sorbed analytes by toluene/methyl tert-butyl ether modified supercritical fluid extraction (SFE), and analysis of the extract by large-volume injection GC-nitrogen/phosphorus detection. The GC system is equipped with a loop-type injection interface with an early solvent vapor exit, a utilizing concurrent solvent evaporation technique. Chemometric approaches, based on a Plackett-Burman screening design and a central composite design for response surface modeling, were used to determine the optimum SFE conditions. The relative standard deviations of the optimized method were determined to be 4.3 to 7.7%, giving raise to method detection limits ranging from 0.06 to 0.36 ng in the sampling cartridge, equivalent to 6.2-36.4 pg/L in the atmosphere, standard sampling volume 10 L. The analytical method was applied to characterize headspace composition above military grade trinitrotoluene (TNT). Results confirm that 2,4-dinitrotoluene (DNT) and 1,3-dinitrobenzene (DNB) constitute the largest vapor flux, but TNT, 2,6-DNT, and trinitrobenzene TNB were also consistently detected in all the samples.

Journal Article↗

On-line coupling of supercritical fluid extraction with high-performance liquid chromatography for the determination of explosives in vapour phases.

An analytical method for determining nitroaromatic explosives in vapour phases is presented. Samples were collected by pumping air through glass fibre filters and polyurethane foam adsorbents, and an on-line extraction system combining supercritical fluid extraction (SFE) and high-performance liquid chromatography (HPLC) was developed. This allows analytes to be transferred from the adsorbent to the HPLC system via a porous graphitic carbon trap. When using gradient elution with a suitable mobile phase, most of the nitroaromatic isomers tested were separated. The proposed method is fully automated, allows a complete analysis to be processed in less than 30 min, and it is compatible with most of the organic solvents commonly used as SFE modifiers or additives. The method has been applied to the analysis of real samples obtained from headspace sampling of military-grade 2,4,6-trinitrotoluene and has been shown to constitute a promising alternative for assessing whether areas are mined in landmine-clearing operations.

Chromatography, High Pressure Liquid↗