Search results for "Standard solution"

showing 10 items of 29 documents

Improved detection limit for ammonium/ammonia achieved by Berthelot's reaction by use of solid-phase extraction coupled to diffuse reflectance spectr…

2005

Abstract The proposed procedure is based on the extraction of the indothylmol blue into C 18 solid-phase extraction (SPE) membranes and direct quantification on the membrane surface by diffuse reflectance spectroscopy. The analytical performance of the proposed method has been evaluated for standard solutions of ammonium using reflectance values, R , as well as the Kubelka–Munk function, F ( R ). The results have been compared with those obtained by the conventional method, which uses UV–vis absorption spectroscopy with a sensor-based method. The described methodology provided satisfactory linearity and reproducibility within the ammonium concentration intervals 25–250 μg L −1 and 25–500 μg…

Detection limitChromatographyDiffuse reflectance infrared fourier transformExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAmmoniachemistry.chemical_compoundchemistryEnvironmental ChemistrySample preparationAmmoniumSolid phase extractionSpectroscopyAnalytica Chimica Acta
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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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A rapid HPLC assay for zearalenone in laboratory cultures ofFusarium graminearum

1993

A high pressure liquid chromatographic (HPLC) method to determine zearalenone in corn contaminated withFusarium graminearum is described. After extraction with methanol-water and solvent partition, samples were cleaned up by applying the extract to a disposable silica cartridge and by eluting the toxin with a mixture of hexane/dry ethyl ether (5/5). Separation was achieved by a reverse phase μBondapak C18 column followed by fluorescence detection using an excitation wavelength at 274 nm and an emission wavelength at 440 nm. Detection limit was about 5 ng. Recoveries ranging from 85.37 to 100.97%, in standard solutions range 30–0.5 µg/ml, were found.

Detection limitChromatographyVeterinary (miscellaneous)Extraction (chemistry)EtherStandard solutionApplied Microbiology and BiotechnologyMicrobiologyHigh-performance liquid chromatographySolventHexanechemistry.chemical_compoundchemistryAgronomy and Crop ScienceZearalenoneMycopathologia
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Flow injection Fourier transform infrared determination of caffeine in coffee

1999

Abstract A fully automatized procedure has been developed for the Fourier transform infrared (FT-IR) spectroscopic determination of caffeine in coffee samples. The method involves the on-line extraction of caffeine with CHCl3. Samples, weighed inside empty PTFE cartridges of 0.5 cm internal diameter (i.d.) and 1.5 ml volume, were humidified with four drops of 0.25 M NH3. The cartridge was installed in a flow manifold, in which samples were extracted in a closed-flow system with 1 ml CHCl3 during 6 min. Four hundred microliters of the extract were introduced in a microflow cell and absorbance measured as a function of time at 1659 cm−1, with a baseline established between 1900 and 830 cm−1, …

Detection limitFlow injection analysisChromatographyAnalytical chemistryStandard solutionAbsorbanceCartridgechemistry.chemical_compoundsymbols.namesakeFourier transformchemistrysymbolsSample preparationCaffeineSpectroscopyVibrational Spectroscopy
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Method development of levoglucosenone analysis by UHPLC-UV-MS in fast pyrolysis samples and aspects of its degradation in aqueous samples

2020

Levoglucosenone ((1S,5R)-6,8-dioxabicyclo[3.2.1]oct-2-en-4-one or LGO; CAS number: 37112-31-5) is an extensively studied biomass based chemical and its potential applications in organic synthesis, as well as in the extraction of various natural substances, have been established; therefore developing dependable, yet fast and simple analytical methods for determining LGO in the products of thermochemical biomass processing is of great importance. In this work different UHPLC methods have been developed and compared for the determination of LGO in wood pyrolysis products. In addition to UV detection, LGO determination conditions by single quadrupole mass spectrometry have been adjusted with an…

ElectrosprayAqueous solutionChromatography010405 organic chemistryGeneral Chemical EngineeringGeneral EngineeringStandard solution010402 general chemistryMass spectrometryFurfural01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistrySample preparationDerivatizationPyrolysisAnalytical Methods
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Assessment of air passive sampling uptakes for volatile organic compounds using VERAM devices

2017

Abstract A calibration chamber has been designed and employed for the simple and easy determination of uptake sampling rate (RS) of volatile organic compounds (VOCs) from air using passive samplers. A flow of clean air was continuously spiked, at a constant VOC concentration, by the microinjection of a standard solution by means of a T-type tube. The developed system allowed the complete evaporation at room temperature of the standard solution in acetone and the air concentration of VOCs was easily controlled by the regulation of the clean air flow, the standard solution concentration and its flow. Active sampling was employed for monitoring the true concentration of the evaluated compounds…

Environmental Engineering010401 analytical chemistryAirflowAnalytical chemistryEvaporationBTEX010501 environmental sciencesStandard solution01 natural sciencesPollutionEthylbenzene0104 chemical scienceschemistry.chemical_compoundchemistryDesorptionEnvironmental chemistryCalibrationEnvironmental ChemistryEnvironmental scienceBenzeneWaste Management and Disposal0105 earth and related environmental sciencesScience of The Total Environment
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Extension of the dynamic range of flame atomic absorption spectrometry using flow injection analysis with variable-volume dilution chambers

1996

Abstract A simple and inexpensive procedure is proposed for the extension of the dynamic range of flame atomic absorption spectrometry measurements using on-line dilution. The proposed methodology is based on the use of a manifold with two coupled dilution chambers and a zone injection system. The samples are prediluted in a closed system which includes a variable-volume mixing chamber (10–120 ml) and two injection valves. The samples are injected through one of these valves, and the other is employed to take 100 μl of prediluted samples which are then passed through a new dilution chamber (volume 1–10 ml) and aspirated by the nebulizer of the instrument. A third injection valve mounted in …

Flow injection analysisChemistryInstrumentationAnalytical chemistryStandard solutionAtomic and Molecular Physics and OpticsAnalytical ChemistryDilutionlaw.inventionStandard curveNebulizerVolume (thermodynamics)lawAtomic absorption spectroscopyInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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Flow injection-FTIR determination of dithiocarbamate pesticides

2000

A flow injection Fourier transform infrared spectrometric procedure has been developed for the determination the dithiocarbamate pesticides Ziram and Thiram in solid samples. All the operations involved, such as extraction, filtration and measurement, were integrated in the experimental set-up in order to avoid excessive manipulation of samples and standards. Ultrasonic assisted and mechanical extraction were evaluated for the solubilization of the analytes and, additionally, the effect of carrier flow rate, sample loop volume and the ratio between sample mass and volume of solvent employed were studied. Quantitative extractions with chloroform were obtained for both Ziram and Thiram, after…

Flow injection analysisDetection limitZiramThiramChromatographyChemistryExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAbsorbancechemistry.chemical_compoundElectrochemistryEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyThe Analyst
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On-line coupling of gel electrophoresis and inductively coupled plasma-sector field-mass spectrometry for the determination of dsDNA fragments.

2005

The on-line coupling of gel electrophoresis (GE) and inductively coupled plasma-mass spectrometry (ICPMS) is described for the first time. The new method combines the separation power of GE for large biomolecules and the high sensitivity and elemental selectivity of ICPMS. This coupling has been achieved by means of gels housed in glass tubes (length 2.5-20 cm; i.d. 0.5-5 mm). The gel is fixed by glass frits permeable for the analytes. After the electrophoretic separation at voltages up to 500 V, the analytes are transferred to the nebulizer of the ICPMS by an eluent stream, which is separated from the electrode chamber by a membrane. This filter blocks molecules with molecular masses large…

Gel electrophoresischemistry.chemical_classificationElectrophoresisChromatographyChemistryBiomoleculeAnalytical chemistryDNAStandard solutionMass spectrometryELECTROPHORESIS INSTRUMENTATIONMass SpectrometryAnalytical ChemistryElectrophoresisColumn chromatographyCalibrationInductively coupled plasmaAnalytical chemistry
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Quantitative colorimetric-imaging analysis of nickel in iron meteorites.

2011

A quantitative analytical imaging approach for determining the nickel content of metallic meteorites is proposed. The approach uses a digital image of a series of standard solutions of the nickel-dimethylglyoxime coloured chelate and a meteorite sample solution subjected to the same treatment as the nickel standards for quantitation. The image is processed with suitable software to assign a colour-dependent numerical value (analytical signal) to each standard. Such a value is directly proportional to the analyte concentration, which facilitates construction of a calibration graph where the value for the unknown sample can be interpolated to calculate the nickel content of the meteorite. The…

INGENIERIA DE LA CONSTRUCCIONbusiness.product_categoryCost effectivenessCalibration curveEconomicsAstronomyAnalytical chemistryImaging analysisStandard solutionCalibration graphsAnalytical ChemistryStandard solutionsDigital imageIron meteoritesSpectro-photometric methodSoftwareNickelCost benefit analysisNational Institutes of HealthProcess engineeringDigital cameraChemistryNumerical valuesMeteoroidsCamerasImageJChemistryAnalytical equipmentPublic domain softwaresSpectrophotometryMeteoriteMeasuring instrumentsColorimetrySpectrophotometersStandardsAnalyte concentrationSample (material)IronColorCost effectivenessArticleColorimetric analysisInstrumentation (computer programming)Digital imageCCDbusiness.industryAnalytical signalsColorimetric-imaging analysisDimethylglyoximeSample solutionVisible spectrophotometrybusinessInstrumentsMeteoritesTalanta
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