A. Pastor

Efficiency of the microwave-assisted extraction of hydrocarbons and pesticides from sediments

Abstract A mixture of toluene and water is proposed for the microwave-assisted extraction of organic pollutants, hydrocarbons and pesticides, from marine sediments. The effect of experimental conditions, such as microwave power and irradiation time, on the extraction of linear, unresolved and polycyclic aromatic hydrocarbons as well as PCBs and DDTs has been evaluated using real marine sediment samples. Values found by Soxhlet and ultrasonic extraction were employed to evaluate the efficiency of the microwave-assisted extraction. Analytical determinations were carried out by gas chromatography using FID, ECD and MS detectors. For 2 g of a dry sediment, an extraction time of 6 min with 10 ml toluene and 1 ml water provides a complete extraction of 15 linear hydrocarbons, 19 polycyclic aromatic hydrocarbons, 4 DDTs and 6 PCBs congeners. Recovery percentage values varies from 107% to 98.5% as compared with the Soxhlet extraction.

Sampling and analysis of pesticides in ambient air.

Developments in the sampling and determination of pesticides in ambient air have been discussed and data on the occurrence of pesticides in atmosphere have been presented. Developments in active sampling methods were reviewed and the different materials used for trapping pesticides from gas and particulate phases were discussed. Likewise, the use and developments of passive air samplers were reviewed. This article pays special attention to the analysis of pesticides trapped from ambient air, and recapitulate the procedures for extraction, clean-up and determination of these substances. Improvements in sampling procedures, analytical methods and monitoring activities are necessary to advance the knowledge of occurrence of currently used pesticides in atmosphere and their impact over environment and humans.

Determination of organic and inorganic mercury species in water and sediment samples by HPLC on-line coupled with ICP-MS

This paper describes a preconcentration method for Hg(2+) and MeHg(+) in water samples using sodium diethyldithiocarbamate immobilized in polyurethane foam (PU-NaDDC) and an extraction method for several mercury species in sediment samples, including MeHg(+), EtHg(+) and PhHg(+), which is simple, rapid, and uses a single organic solvent. Separation and measurement were done by high-performance liquid chromatography on-line with inductively coupled plasma mass spectrometry (HPLC/ICP-MS). Initially, the test of recovery was applied using procedures compatible with HPLC. Under the optimum extraction conditions, recoveries of 96.7, 96.3 and 97.3% were obtained for MeHg(+), EtHg(+), and PhHg(+), respectively, from n=4 spiked sediment samples. This study also demonstrates that the combination of solid-phase extraction on PU-NaDDC with HPLC separation and ICP-MS detection is an effective preconcentration procedure for simultaneous measurement of Hg(2+) and MeHg(+) at ultra-trace levels in water samples. The application of the proposed procedure to the determination of mercury species in drinking water sample was investigated. The proposed method clearly gave satisfactory average recoveries between 93.7 and 101.5%.

Determination of PAHs in airborne particles by accelerated solvent extraction and large-volume injection-gas chromatography-mass spectrometry

A sensitive and automated method is presented for the determination of polycyclic aromatic hydrocarbons (PAHs) in airborne particulate matter. The procedure includes extraction of PM10-bound PAHs by accelerated solvent extraction (ASE) followed by gel permeation chromatography (GPC) clean-up, and large-volume programmable temperature vaporizer (PTV-LV) injection coupled to GC-MS. The limit of detection (LOD) of the whole method, based on a signal-to-noise ratio (S/N) of 3:1, ranged from 0.26pgm(-3) to 3pgm(-3) when air volumes of 760m(3) are collected. The hexane-acetone mixture (1:1, v/v) gave the best recoveries when ASE parameters were fixed at 125 degrees C, 1500psi, and a total time of 10min. The recoveries for all PAHs tested ranged from 96% to 103%, rates similar to those obtained by the Soxhlet reference method. To improve the sensitivity, 70muL were injected. The PTV-LV injection settings were optimized using a statistical design of experiments, including a screening 2(4) full factorial design and a further central composite design. A sensitivity increase from 10 to 50 times was achieved as compared with the conventional 2muL splitless injection. The method was validated with the standard reference material SRM 1649a and applied to real PM10 samples from the monitoring network of the Regional Valencia Government (Spain). The analytical performance of the method shows that it is appropriate to monitor PAHs levels in ambient air according to European Union Directives. In addition, the method can be used when a high sensitivity is required.

Chemometric determination of arsenic and lead in untreated powdered red paprika by diffuse reflectance near-infrared spectroscopy.

It has been evaluated the potential of near-infrared (NIR) diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) as a way for non-destructive measurement of trace elements at microg kg(-1) level in foods, with neither physical nor chemical pre-treatment. Predictive models were developed using partial least-square (PLS) multivariate approaches based on first-order derivative spectra. A critical comparison of two spectral pre-treatments, multiplicative signal correction (MSC) and standard normal variate (SNV) was also made. The PLS models built after using SNV provided the best prediction results for the determination of arsenic and lead in powdered red paprika samples. Relative root-mean-square error of prediction (RRMSEP) of 23% for both metals, arsenic and lead, were found in this study using 20 well characterized samples for calibration and 13 additional samples as validation set. Results derived from this study showed that NIR diffuse reflectance spectroscopy combined with the appropriate chemometric tools could be considered as an useful screening tool for a rapid determination of As and Pb at concentration level of the order of hundred microg kg(-1).

Relationships between sediment physico-chemical characteristics and heavy metal bioaccumulation in Mediterranean soft-bottom macrophytes

Abstract Concentrations of Hg, Cd, Pb and Zn in the two seagrasses ( Posidonia oceanica and Cymodocea nodosa ), green alga Caulerpa prolifera and sediment and some physico-chemical characteristics of the sediment (organic matter, fine fraction (particles Significant correlations between the concentrations of metals in the plants and sediment (alone or normalized with respect to the physico-chemical characteristics) were usually found for Hg and Zn. For Pb only C . prolifera fractions were correlated to the Pb content of the sediment. For Cd no significant correlations were obtained between the metal in the plants and sediment. The concentration factors of the metals in the plants with respect to sediment were usually negatively correlated with the fine fraction, organic matter and CEC of the sediment for Hg, Pb and Zn in Posidonia and Cymodocea , and for Hg and Zn in Caulerpa . This suggests that these variables of the sediment increase the retention of these metals in the sediment and reduce their availability to the plants. Stepwise multiple regression analyses yielded only three equations with at least two independent variables in the model: the Hg concentration in leaves and roots of Posidonia oceanica is explained by the Hg concentration of the sediment and organic matter of the sediment. The Hg concentration in the fronds of Caulerpa prolifera is explained by the Hg concentration in the sediment and by the carbonate content of the sediment.

Searching the Most Appropriate Sample Pretreatment for the Elemental Analysis of Wines by Inductively Coupled Plasma-Based Techniques

Different sample preparation methods were evaluated for the simultaneous multielement analysis of wine samples by inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS). Microwave-assisted digestion in closed vessel, thermal digestion in open reactor, and direct sample dilution were considered for the determination of Li, Be, Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Sr, Y, Mo, Cd, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Tl, Pb, and Bi in 12 samples of red wine from Valencia and Utiel-Requena protected designation of origin. ICP-MS allows the determination of 17 elements in most of the samples, and using ICP-OES, a maximum of 15 elements were determined. On comparing the sample pretreatment methodology, it can be concluded that the three assayed procedures provide comparable results for the concentration of Li, Na, Mg, Al, K, Ca, Mn, Fe, Zn, and Sr by ICP-OES. Furthermore, ICP-MS data found for Cu, Pb, and Ba were comparable. Digestion treatment provides comparable values using both total decomposition in open system and microwave-assisted treatment for Cu by ICP-OES and for Cr, Ni, and Zn by ICP-MS. Open vessel total digestion provides excess values for Cr, Mn, Fe, and Zn by ICP-OES and defect values for Se. However, direct measurement of diluted wine samples provided uncomparable results with the digestion treatment for Mn, Cu, Pb, Zn, Ba, and Bi by ICP-OES and for Mg, Cr, Fe, Ni, and Zn by ICP-MS. Therefore, it can be concluded that microwave-assisted digestion is the pretreatment procedure of choice for elemental analysis of wine by ICP-based techniques.

Determination of arsenic compounds in beverages by high-performance liquid chromatography-inductively coupled plasma mass spectrometry.

Arsenic compounds including arsenous acid (As(III)), arsenic acid (As(V)), dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA) were separated by high-performance liquid chromatography (HPLC) and detected by inductively coupled plasma mass spectrometry (ICP-MS). A Hamilton PRX-100 anionic-exchange column and a pH 8.5 K(2)HPO(4)/KH(2)PO(4) 5.0x10(-3)molL(-1) mobile phase were used to achieve arsenic speciation. The separation of arsenic species provided peaks of As(III) at 2.75min, DMA at 3.33min, MMA at 5.17min and As(V) at 12.5min. The detection limits, defined as three times the standard deviation of the lowest standard measurements, were found to be 0.2, 0.2, 0.3 and 0.5ngmL(-1) for As(III), DMA, MMA and As(V), respectively. The relative standard deviation values for a solution containing 5.0mugL(-1) of As(III), DMA, MMA and As(V) were 1.2, 2.1, 2.5 and 3.0%, respectively. This analytical procedure was applied to the speciation of arsenic compounds in drinking (soft drink, beer, juice) samples. The validation of the procedure was achieved through the analysis of arsenic compounds in water and sediment certified reference materials.

Monitoring programme on cadmium, lead and mercury in fish and seafood from Valencia, Spain: levels and estimated weekly intake.

The study was carried out to determine the current levels of mercury, cadmium, and lead in fish and seafood from the market of Comunitat Valenciana, Spain. Levels of total mercury ranged from 0.02 to 3.15 mg kg−1 w.w. (average = 0.073 mg kg−1 w.w.). Cadmium concentrations ranged from 0.003 to 0.66 mg kg−1 w.w. (average = 0.27 mg kg−1 w.w.) for seafood, and between 0.003 and 0.71 mg kg−1 w.w. (average = 0.01 mg kg−1 w.w.) for marine fish. Concerning lead, concentrations from 0.02 to 0.36 mg kg−1w.w (average = 0.04 mg kg−1 w.w.) were found in fish, and from 0.02 to 1.02 mg kg−1 w.w. in seafood (average = 0.147 mg kg−1 w.w.). The levels found were, in general, lower than maximum levels proposed by European legislation. The estimated weekly intake of mercury, cadmium and lead through fish and seafood consumption was found to be about 43%, 10% and 3% of the established provisional tolerable weekly intake, respectively.

Comprehensive analytical strategy for biomonitoring of pesticides in urine by liquid chromatography–orbitrap high resolution mass spectrometry

In this study we propose an analytical strategy that combines a target approach for the quantitative analysis of contemporary pesticide metabolites with a comprehensive post-target screening for the identification of biomarkers of exposure to environmental contaminants in urine using liquid chromatography coupled to high-resolution mass spectrometry (LC–HRMS). The quantitative method for the target analysis of 29 urinary metabolites of organophosphate (OP) insecticides, synthetic pyrethroids, herbicides and fungicides was validated after a previous statistical optimization of the main factors governing the ion source ionization and a fragmentation study using the high energy collision dissociation (HCD) cell. The full scan accurate mass data were acquired with a resolving power of 50,000 FWHM (scan speed, 2 Hz), in both ESI+ and ESI− modes, and with and without HCD-fragmentation. The method – LOQ was lower than 3.2 μg L−1 for the majority of the analytes. For post-target screening a customized theoretical database was built, for the identification of 60 metabolites including pesticides, PAHs, phenols, and other metabolites of environmental pollutants. For identification purposes, accurate exact mass with less than 5 ppm, and diagnostic ions including isotopes and/or fragments were used. The analytical strategy was applied to 20 urine sample collected from children living in Valencia Region. Eleven target metabolites were detected with concentrations ranging from 1.18 to 131 μg L−1. Likewise, several compounds were tentatively identified in the post-target analysis belonging to the families of phthalates, phenols and parabenes. The proposed strategy is suitable for the determination of target pesticide biomarkers in urine in the framework of biomonitoring studies, and appropriate for the identification of other non-target metabolites.