Search results for "Peat"

showing 10 items of 1026 documents

Determination of cyromazine in pesticide commercial formulations by vibrational spectrometric procedures

2004

Two vibrational spectrometry-based methodologies were developed for Cyromazine determination in solid pesticide formulations: a Fourier transform infrared (FTIR) procedure, based on the extraction of Cyromazine by CH3OH and direct determination in the extracts by peak height measurement at 1622 cm−1 corrected using a baseline defined at 1900 cm−1, and a FT-Raman determination, made directly on the powdered solid products using standard chromatographic glass vials as sample cells and measuring the Raman intensity between 633 and 623 cm−1 for a baseline established between 663 and 601 cm−1. The sensitivity obtained was 0.01631 absorbance g−1 mg for FTIR determination and 2.23 area values g−1 …

Detection limitChromatographyExtraction (chemistry)Analytical chemistryRepeatabilityCyromazineBiochemistryFourier transform spectroscopyAnalytical ChemistryAbsorbancechemistry.chemical_compoundchemistryEnvironmental ChemistrySample preparationFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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Mid- and near-infrared determination of metribuzin in agrochemicals

2008

Abstract Two infrared-based methodologies were developed for metribuzin determination in pesticide formulations after extraction with acetonitrile. Fourier transform mid infrared (MIR) procedure was based on peak area measurements between 1692 and 1670 cm −1 corrected with a baseline fixed at 1877 cm −1 . Fourier transform near infrared (NIR) determination was made by measuring the peak area between 6498 and 6332 cm −1 corrected using a two points baseline defined between 6570 and 6212 cm −1 . Repeatability, as relative standard deviation, of 5 independent measurements at mg g −1 concentration level was 0.3% and 0.03% for MIR and NIR, respectively, and limit of detection values of 9 and 17 …

Detection limitChromatographyInfraredChemistryNear-infrared spectroscopyExtraction (chemistry)Analytical chemistryRepeatabilitychemistry.chemical_compoundsymbols.namesakeFourier transformMetribuzinsymbolsAcetonitrileSpectroscopyVibrational Spectroscopy
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry Analysis of Carbosulfan, Carbofuran, 3-Hydroxycarbofuran, and Other Metabolites in …

2007

The potential of liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QqTOF-MS) to identify and confirm carbosulfan and seven of its main metabolites (carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenol carbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran, dibutylamine) at trace levels from food is explored for the first time. The analytical method developed consists of pressurized liquid extraction (PLE) and LC-QqTOF-MS in positive ion mode, which attains unequivocal identification and quantification of the studied compounds in food, at levels well below of those of concern (0.05 mg/kg for the sum of carbosulfan, carbofuran, and 3-hydroxycarbofuran).…

Detection limitChromatographyMolecular StructureMetaboliteRepeatabilityButylaminesMass spectrometrySensitivity and SpecificityAnalytical ChemistryDibutylamineCarbofuranchemistry.chemical_compoundchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCarbosulfanCarbamatesQuantitative analysis (chemistry)CarbofuranFood AnalysisChromatography LiquidAnalytical Chemistry
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An environmentally friendly multicommutated alternative to the reference method for anionic surfactant determination in water

2004

Abstract It has been developed a fully mechanized procedure for the spectrophotometric determination of anionic surfactants in water expressed in terms of SDS concentration. The reference method, based on the reaction of SDS with methylene blue (MB) followed by extraction in chloroform, was mechanized in order to reduce the consumption of organic solvents. The system was based on the multicommutation approach and provided a 35 times reduction of the waste production without sacrificing the figures of merit of the method in terms of sensitivity and repeatability, for a dynamic linear range from 0.2 to 1.7 mg l−1. Results obtained for washing water samples were comparable with those obtained …

Detection limitChromatographymedicine.diagnostic_testChemistryExtraction (chemistry)Analytical chemistryRepeatabilityAnalytical ChemistrySolventPulmonary surfactantLinear rangeSpectrophotometrymedicineSample preparationTalanta
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Determination of n-alkanes, PAHs and hopanes in atmospheric aerosol: evaluation and comparison of thermal desorption GC-MS and solvent extraction GC-…

2019

Organic aerosol (OA) constitutes a large fraction of fine particulate matter (PM) in the urban air. However, the chemical nature and sources of OA are not well constrained. Quantitative analysis of OA is essential for understanding the sources and atmospheric evolution of fine PM, which requires accurate quantification of some organic compounds (e.g., markers). In this study, two analytical approaches, i.e., thermal desorption (TD) gas chromatography-mass spectrometry (GC-MS) and solvent extract (SE) GC-MS were evaluated for the determination of n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and hopanes in ambient aerosol. For the SE approach, the recovery obtained is 89.3–101.5&…

Detection limitEnvironmental chemistryThermal desorptionEnvironmental scienceCoal combustion productsFraction (chemistry)Repeatability010501 environmental sciencesGas chromatography–mass spectrometryMass spectrometry01 natural sciences0105 earth and related environmental sciencesAerosol
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Comparison of different methods for extraction of polycyclic aromatic hydrocarbons (PAHs) from Sicilian (Italy) coastal area sediments.

2012

This paper describes a work aimed at improving the conditions of an extraction method, coupling GC-MS determination, for the analysis without cleanup phase, of polycyclic aromatic hydrocarbons (PAHs) from sediment samples. The automatic Soxhlet extraction in warm mode (using Extraction System B-811 Standard, Buchi) has demonstrated advantages for automation, reduced extraction time, and lower solvent use than for conventional Soxhlet extraction. Under these conditions, the recoveries are very good as they resulted greater than 85 % and, in most of the cases, near 100 %. The repeatability is also satisfactory (relative standard deviation less than 15 %). The detection limits are also accepta…

Detection limitGeologic SedimentsExtraction (chemistry)SedimentGeneral MedicineRepeatabilityChemical FractionationManagement Monitoring Policy and LawPollutionGas Chromatography-Mass SpectrometrySettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Dry weightEnvironmental chemistryEnvironmental scienceEcotoxicologySeawaterSettore CHIM/01 - Chimica AnaliticaPolycyclic Aromatic HydrocarbonsGas chromatography–mass spectrometryAutomatic extraction .CRM . PAHs . Sediments . GC-MSSicilyWater Pollutants ChemicalEnvironmental MonitoringGeneral Environmental Science
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Introducing a new and rapid microextraction approach based on magnetic ionic liquids: Stir bar dispersive liquid microextraction

2017

With the aim of contributing to the development and improvement of microextraction techniques, a novel approach combining the principles and advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) is presented. This new approach, termed stir bar dispersive liquid microextraction (SBDLME), involves the addition of a magnetic ionic liquid (MIL) and a neodymium-core magnetic stir bar into the sample allowing the MIL coat the stir bar due to physical forces (i.e., magnetism). As long as the stirring rate is maintained at low speed, the MIL resists rotational (centrifugal) forces and remains on the stir bar surface in a manner closely resembling SBS…

Detection limitMagnetic ionic liquidChromatographyChemistryMagnetism010401 analytical chemistryExtraction (chemistry)Analytical chemistryThermal desorption02 engineering and technologyRepeatability021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundIonic liquidEnvironmental Chemistry0210 nano-technologySpectroscopyBar (unit)Analytica Chimica Acta
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Calibration of LA-ICP-MS via standard addition using dried picoliter droplets

2020

A novel microanalytical calibration approach for quantitative spatially resolved analysis of thin layered materials with laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) is presented. This method relies on standard addition via the generation of dried pL-droplet residues. Therefore, a drop on demand dosing device based on a modified commercial ink cartridge and a dosing interface, both accessible via a self-constructed microcontroller, were developed. This dosing device enables the precise deposition of pL-droplets onto solid samples for the generation of residues with dimensions in the low μm-range. The LA-ICP-MS analysis of such residues allows calibration over at l…

Detection limitMaterials scienceThin sectionSample (material)010401 analytical chemistryAnalytical chemistry02 engineering and technologyRepeatability021001 nanoscience & nanotechnologyMass spectrometryLaser01 natural sciences0104 chemical sciencesAnalytical Chemistrylaw.inventionCartridgelawStandard addition0210 nano-technologySpectroscopyJournal of Analytical Atomic Spectrometry
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Determination of N -nitrosamines in cosmetic products by vortex-assisted reversed-phase dispersive liquid-liquid microextraction and liquid chromatog…

2018

A new analytical method for the simultaneous determination of trace levels of seven prohibited N-nitrosamines (N-nitrosodimethylamine, N-nitrosoethylmethylamine, N-nitrosopyrrolidine, N-nitrosodiethylamine, N-nitrosopiperidine, N-nitrosomorpholine, and N-nitrosodiethanolamine) in cosmetic products has been developed. The method is based on vortex-assisted reversed-phase dispersive liquid-liquid microextraction, which allows the extraction of highly polar compounds, followed by liquid chromatography with mass spectrometry. The variables involved in the extraction process were studied to obtain the highest enrichment factor. Under the selected conditions, 75 μL of water as extraction solvent …

Detection limitNitrosaminesMaterials scienceChromatographyMolecular StructureLiquid Phase Microextraction010401 analytical chemistryExtraction (chemistry)Mixing (process engineering)Filtration and SeparationCosmetics02 engineering and technologyRepeatability021001 nanoscience & nanotechnologyMass spectrometry01 natural sciencesMass Spectrometry0104 chemical sciencesAnalytical ChemistrySolventPhase (matter)0210 nano-technologyEnrichment factorChromatography LiquidJournal of Separation Science
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Validating quantitative PCR assays for cell-free DNA detection without DNA extraction: Exercise induced kinetics in systemic lupus erythematosus pati…

2021

ABSTRACTCirculating cell-free DNA (cfDNA) has been investigated as a screening tool for many diseases. To avoid expensive and time-consuming DNA isolation, direct quantification PCR assays can be established. However, rigorous validation is required to provide reliable data in the clinical and non-clinical context. Considering International Organization for Standardization, as well as bioanalytical method validation guidelines we provide a comprehensive procedure to validate assays for cfDNA quantification from unpurified blood plasma. A 90 and 222 bp assay was validated to study the kinetics of cfDNA after exercise in patients with systemic lupus erythematosus. The assays showed ultra-low …

Detection limitOncologymedicine.medical_specialtyBioanalysisbusiness.industryContext (language use)RepeatabilityDNA extractionReal-time polymerase chain reactionCell-free fetal DNAInternal medicineBlood plasmamedicinebusiness
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