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Yoann Fillâtre David Rondeau Antoine Daguin Alain Jadas-Hecart Pierre-Yves Communal 《Analytical and bioanalytical chemistry》2014,406(5):1541-1550
The determination of 256 multiclass pesticides in lavandin essential oil has been performed by liquid chromatography–electrospray ionization tandem mass spectrometry using the scheduled selected reaction monitoring mode available on a quadrupole-linear ion trap mass spectrometer. With the aim of improving the limits of quantification (LOQs) of the target molecules, a sampling step based on evaporation of the essential oil under a nitrogen flow assisted by controlled heating was tested. The LOQs determined in this case were compared with the values obtained with the classic dilution preparation method. With sampling by dilution, 247 pesticides were detected and quantified at low concentration, with 74 % of the pesticides having LOQs of 10 μg L-1 or less. With the evaporation method, a global improvement of the LOQs was observed, with lower LOQs for 92 active substances and LOQs of 10 μg L-1 or less for 82.8 % of the pesticides. Almost twice as many active substances had an LOQ of 1 μg L-1 or less when the evaporation method was used. Some pesticides exhibited poor recovery or high variance caused by volatilization or degradation during the evaporation step. This behavior was evidenced by the case of thiophanate-methyl, which is degraded to carbendazim. Figure
Sampling method by dilution or evaporation in the multiresidue determination of pesticides in essential oils by LC/MS 相似文献
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Cécile Arbez-Gindre George A. Heropoulos Jean-Edouard Communal Isabelle Ledoux-Rak 《Journal of organometallic chemistry》2005,690(6):1620-1626
A series of triarylmethanol derivatives containing combinations of phenyl, 1-naphthyl, 4-dimethylamino-4′-stilbenyl, ferrocenyl or 4-[2-ferrocenylethenyl]phenyl groups have been prepared by reaction of 4-[4-Me2NC6H4CC]C6H4Li or 4-[FcCC]C6H4Li (Fc = ferrocenyl) with ferrocenecarboxaldehyde, ferrocenyl phenyl ketone, methyl ferrocenecarboxylate, 1-naphthyl phenyl ketone, ethyl benzoate or diethyl carbonate. The carbinols readily form the corresponding intensely coloured carbenium ions in acid solution which have significant electronic absorption in the near infrared. Initial studies indicate that they also possess substantial first hyperpolarisabilities. 相似文献
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Béguin S Jadas-Hécart A Tabet JC Communal PY 《Journal of mass spectrometry : JMS》2006,41(10):1304-1314
The product ion spectrum allows us to achieve very selective detection of pesticides and to eliminate the ambiguities caused by more conventional analytical approaches. Owing to the enhanced capabilities of GC/MS/MS for multiresidue pesticides, the development of a GC/MS/MS pesticides library will be useful. The aim of this study was to develop a sensitive and specific analytical method for the identification and quantification of compounds without the need of a time-consuming procedure. Two methods were studied in order to optimize the nonresonant conditions of dissociation of five pesticides (deltamethrin, metalaxyl, myclobutanil, procymidone, pirimicarb). The first permits a systematic investigation of the influence of the qz trapping parameter on sensitivity in precursor ion detection and on the efficiency of collision-induced dissociation (CID). The second is more suited for analytical laboratories and less time-consuming and allows us to reach similar results: the experiments were conducted step by step at a constant stability parameter. 相似文献
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An analytical method has been developed for the determination of residues of ethephon (2-chloroethyl phosphonic acid) in drinking and surface water. The procedure is based on de-ionisation with an anion/cation-exchange resin, solid phase extraction by means of anion-exchange polystyrene-divinylbenzene extraction disks, elution with a mixture of methanol and 10 M hydrochloric acid (98/2, v/v), redisolution into acetonitrile after evaporation and silylation with N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA). Quantification is performed by gas chromatography with ion-trap cubic mass spectrometric detection in the electron impact mode (GC-EI-MS3). Method validation was conducted using samples of mineral, tap, and river water that were fortified with ethephon at concentration levels ranging from 0.1 to 1.0 microg/L. The mean recovery from all the fortified samples (n = 36) amounted to 88% with a relative standard deviation of 17%. The method, therefore, was shown to allow accurate determination of ethephon residues in drinking and surface water with a limit of quantification of 0.1 microg/L. 相似文献
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