Search results for "PEST"

showing 10 items of 1124 documents

Analytical strategy photodegradation/chemiluminescence/continuous-flow multicommutation methodology for the determination of the herbicide Propanil

2006

The present paper is dealing with an analytical strategy based on coupling photodegradation, chemiluminescence and multicommutation continuous-flow methodology for the determination of the pesticide Propanil, a common herbicide. The pesticide solution is inserted as small segments sequentially alternated with segments of the solution for adjusting the suitable medium for the photodegradation. Both flow-rates (sample and medium) are adjusted to required time for photodegradation, 2.0 min; and then, the resulting solution is also sequentially inserted as segments alternated with segments of the oxidizing solutions system, 1.00 x 10(-4) mol 1(-1) potassium permanganate in 2.00 mol 1(-1) sulphu…

Detection limitChromatographyChemiluminescenceCorrelation coefficientChemistryAlachlorAnalytical chemistryRepeatabilityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatePhotoreactionlawMulticommutationPropanilQUIMICA ANALITICAPesticidesPhotodegradationChemiluminescence
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On-line preconcentration strategies for analyzing pesticides in fruits and vegetables by micellar electrokinetic chromatography.

2007

Five pesticides (fludioxonil, procymidone, pyriproxyfen, dinoseb and carbendazim) were separated in reversed migration micellar electrokinetic chromatography (RM-MEKC) using 20 mmol l(-1) phosphate buffer at pH 2.3, containing 25 mmol l(-1) sodium dodecylsulfate and 10% methanol. Three on-line concentration strategies, sweeping (SW), normal stacking with reversed migration and a water plug (SRW) and stacking with reverse migration and removal of sample matrix using polarity switching (SRMM), were compared. About 10-, 30- and 50-fold increases in detection sensitivity, compared with standard hydrodynamic injection (5 s at 0.5 psi), were observed with SW, SRW and SRMM, respectively. Limits of…

Detection limitChromatographyChemistryCarbendazimOrganic ChemistryAnalytic Sample Preparation MethodsElectrophoresis CapillaryGeneral MedicineBiochemistryOnline SystemsMicellar electrokinetic chromatographyAnalytical ChemistryFungicides Industrialchemistry.chemical_compoundElectrophoresisFruitDinosebVegetablesSample preparationSolid phase extractionProcymidonePesticidesFood AnalysisChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Solid-Phase Microextraction Liquid Chromatography/Tandem Mass Spectrometry To Determine Postharvest Fungicides in Fruits

2003

A method to determine five postharvest fungicides (dichloran, flutriafol, o-phenylphenol, prochloraz, tolclofos methyl) in fruits (cherries, lemons, oranges, peaches) has been developed using solid-phase microextraction (SPME) coupled to liquid chromatography (LC) with photodiode array (DAD), mass spectrometry (MS), or tandem mass spectrometry (MS/MS) with ion trap detection. Extraction involved sample homogenization with an acetone/water solution (5:1), filtration, and acetone evaporation prior to fiber extraction. The pesticides were isolated with a fused-silica fiber coated with 50-microm Carbowax/template resin. The effects of pH, ion strength, sample volume, and extraction time were in…

Detection limitChromatographyChemistryPesticide ResiduesReference StandardsSolid-phase microextractionMass spectrometryTandem mass spectrometryMass SpectrometryFungicides IndustrialAnalytical ChemistryLiquid chromatography–mass spectrometryFruitDesorptionCalibrationIndicators and ReagentsSpectrophotometry UltravioletSample preparationIon trapChromatography LiquidAnalytical Chemistry
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Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.

2003

A method based on solid-phase microextraction (SPME) and capillary electrophoresis/mass spectrometry (CE/ MS) is described for determining simultaneously five acidic pesticides (o-phenylphenol, ioxynil, haloxyfop, acifluorfen, picloram) in fruits. The CE device is coupled to an electrospray interface by a commercial sheath-flow adapter. Emphasis is placed on fulfillment of the speed and sensitivity requirements. The best separation is achieved using 32 mM ammonium formate/acid formic buffer at pH 3.1, with a working voltage of 25 kV. The MS detection of the five pesticides was performed in negative ionization mode. Full-scan spectra with base peaks corresponding to [M-H]- were obtained exce…

Detection limitChromatographyChemistryPlant ExtractsAnalytical chemistryElectrophoresis CapillaryFood ContaminationAcifluorfenMass spectrometrySolid-phase microextractionCapillary electrophoresis–mass spectrometryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisFruitAmmonium formateSample preparationPesticidesAnalytical chemistry
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Simultaneous quantification of serum phytosterols and cholesterol precursors using a simple gas chromatographic method

2012

Determination of the main phytosterols (Ps, β-sitosterol and campesterol) and cholesterol precursors (desmosterol and lathosterol) in human serum using a simple GC-FID method has been validated. Direct saponification, without lipid extraction, sterols extraction, and further derivatization was applied to samples prior to GC analysis. To evaluate the method, a pool of serum samples from eight healthy women was used. Good linearity (r>0.99) was found in the assay range: β-sitosterol (0.99–17.82 µg/mL), campesterol (0.14–10.8 µg/mL), desmosterol (0.17–2.6 µg/mL), and lathosterol (0.6–5.97 µg/mL). Limits of detection (ng/mL) were: 86 (β-sitosterol), 42 (campesterol), 4 (desmosterol), and 44 (la…

Detection limitChromatographyCholesterolCampesterolLathosterolGeneral ChemistryIndustrial and Manufacturing Engineeringchemistry.chemical_compoundchemistryDesmosterollipids (amino acids peptides and proteins)Gas chromatographyDerivatizationSaponificationFood ScienceBiotechnologyEuropean Journal of Lipid Science and Technology
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Evaluation of working air quality by using semipermeable membrane devices

2008

Abstract It has been evaluated the use of semipermeable membrane devices (SPMDs) as passive samplers of organophosphorus pesticides from air, in order to determine the contamination of working environments. Additionally, the use of SPMDs as portable samplers has been also considered. The analytical methodology for the determination of diazinon, chlorpyrifos-methyl, pirimiphos-methyl, chlorpyrifos and fenthion in SPMDs exposed to contaminated air was based on microwave-assisted extraction and gas chromatography with mass spectrometry determination. Limit of detection (LOD) values from 2 to 4 ng SPMD−1 and repeatability from 2 to 7% were obtained by using the aforementioned methodology. Theor…

Detection limitChromatographyDiazinonAir pollutionPesticideContaminationmedicine.disease_causeBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryChlorpyrifosEnvironmental chemistrymedicineEnvironmental ChemistryGas chromatographyAir quality indexSpectroscopyAnalytica Chimica Acta
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A chemiluminescence flow-based procedure for determination of carbaryl in natural waters exploiting multicommutation and enzymatic reaction

2007

A chemiluminescence procedure for the determination of carbaryl in natural waters using acetylcholinesterase and choline oxidase is described. The flow system designed to implement multicommutation approach controlled by microcomputer comprised five solenoid valves, two columns with immobilized enzymes on controlled pore glass beads and chemiluminometric flow cell. In the best experimental conditions a linear response ranging from 25 to 700 µg L-1 carbaryl was obtained. Water samples were spiked with carbaryl in order to access the accuracy and recoveries between 95 and 101% were obtained for a concentration level ranging from 25 to 100 µg L-1 carbaryl. Detection limit and variation coeffic…

Detection limitChromatographyImmobilized enzymeChemistryPotassiumchemistry.chemical_elementGeneral ChemistryCholine oxidasechemiluminescenceLuminollaw.inventionpesticide carbarylchemistry.chemical_compoundmulticommutationlawReagentCarbarylflow analysisChemiluminescenceenzymatic reaction
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Uptake and translocation monitoring of imidacloprid to chili and tomato plants by molecularly imprinting extraction - ion mobility spectrometry

2019

Abstract The degradation of imidacloprid in soil and its uptake and translocation to chili and tomato plants was evaluated, as a proof of concept, of the possibilities of the combination of molecularly imprinted polymers (MIPs) and ion mobility spectrometry (IMS) for a fast and sensitive bioprocesses monitoring tool. To do it, a method based on the selective extraction of imidacloprid from soil and plant materials was developed. In the selected conditions, the MIP-IMS procedure provided a recovery of imidacloprid in soil and plant samples from 102 to 114%, for spiked concentration levels from 0.2 to 2.0 μg g−1. Precision of the methodology, expressed as the relative standard deviation (RSD)…

Detection limitChromatographyIon-mobility spectrometryChemistry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymerChromosomal translocation02 engineering and technologyPesticideStandard solution021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundImidacloprid0210 nano-technologySpectroscopyMicrochemical Journal
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Fourier transform infrared determination of imidacloprid in pesticide formulations

2004

A simple method has been developed for Fourier Transform Infrared (FTIR) determination of Imidacloprid in pesticide formulations. Samples were diluted with CHCl3 and the FTIR spectra of samples and standards were obtained at a nominal resolution of 4 cm-1 from 4000 to 900 cm-1 accumulating 25 scans. Imidacloprid determination was based on the measure of either peak area from 1577 to 1567 cm-1 or peak height at 1572 cm-1, both corrected using a horizontal baseline defined at 1900 cm-1. The limits of detection achieved, of the order of 9 µg g-1, were appropriate for the determination of Imidacloprid in commercially available formulations. FTIR results were statistically comparable to those fo…

Detection limitChromatographyMaterials scienceHPLC-UVResolution (mass spectrometry)InfraredImidaclopridGeneral ChemistryHigh-performance liquid chromatographylcsh:Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformchemistrylcsh:QD1-999FTIRImidaclopridsymbolsSample preparationFourier transform infrared spectroscopypesticide formulations
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Determination of amitraz and its transformation products in pears by ethyl acetate extraction and liquid chromatography-tandem mass spectrometry.

2008

A method has been developed for identification and quantification of the acaricide amitraz and its transformation products, 2,4-dimethylaniline (DMA), 2,4-dimethylformamidine (DMF) and N-2,4-dimethylphenyl-N-methylformamidine (DMPF) in pears. The analytes were extracted using ethyl acetate and anhydrous sodium sulphate. Analysis was performed by liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode using a triple quadrupole (QqQ) instrument. Two precursor-product ion transitions were monitored for each compound in the selected reaction monitoring (SRM) mode. The method was validated with pears taken from the orchard before the amitraz treatment …

Detection limitChromatographyMaximum Residue LimitAniline CompoundsToluidinesSulfatesOrganic ChemistrySelected reaction monitoringEthyl acetatePesticide ResiduesReproducibility of ResultsGeneral MedicineAcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerPyruschemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryAmitrazChromatography LiquidJournal of chromatography. A
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