Search results for "chemical analysis"

showing 10 items of 324 documents

Control of matrix interferences by the multiple linear regression model in the determination of arsenic, antimony and tin in lead pellets by inductiv…

2002

A multiple linear regression technique was used to evaluate the matrix interferences in the determination of hydride-forming elements in lead shotgun pellets by inductively coupled plasma atomic emission spectrometry. The determination of arsenic, antimony, and tin in SRM C2416 (Bullet Lead) by ICP-AES failed to obtain the certified concentrations at the 95% level of confidence using the t-test. However, it proved possible, by using the multiple linear regression technique, to correct the concentrations of all three elements to a statistically acceptable level. This method of correction is based on the multiple regression line obtained from the analysis of 19 synthetic mixtures of matrix el…

RadiochemistryAnalytical chemistrychemistry.chemical_elementequipment and suppliesCopperAnalytical ChemistryBismuthMatrix (chemical analysis)chemistryAntimonyLinear regressionInductively coupled plasmaTinSpectroscopyArsenicJ. Anal. At. Spectrom.
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Electrochemical characterization of mangrove sediments: A proposal of new proxies for organic matter oxidation

2019

Abstract The voltammetric response of microparticulate deposits resulting from solvent evaporation of ethanolic extracts of mangrove sediments in contact with aqueous acetate buffer is hereby described. Dated sediment cores sampled from the Peruvian mangrove system (“Manglares de Tumbes” National Sanctuary) presented voltammetric responses dominated by oxidative signals of organic components that exhibit significant variations depending on the depth. Voltammetric data allowed for the definition of electrochemical indexes representative of the electrochemically oxidable organic matter fraction. These electrochemical indexes were fEAOM (for the total amount of organic matter being electrochem…

Redox state010501 environmental sciences010502 geochemistry & geophysicsElectrochemistryMangrove sediments01 natural sciencesevaporationPeruElectrochemistryChemical analysisInfrared spectroscopyorganic matterchemistry.chemical_classificationAqueous solutionChemistryBiogeochemistryPollutionOrganic matter oxidationEnvironmental chemistryOrganic matter degradationsMangroveoxidationInfrared spectroscopyredox conditionssolventSedimentsVoltammetric responseGeochemistry and PetrologyOrganic compoundsOrganic matter fractionEnvironmental ChemistryOrganic matter14. Life underwaterSpectroscopyOxidation proxies0105 earth and related environmental sciencesparticulate mattermangrove//purl.org/pe-repo/ocde/ford#1.05.00 [https]SedimentBiological materials15. Life on landcoastal sedimentElectrochemical characterizationssediment coreSolvent evaporationVoltammetryethanolacetateaqueous solutionReactive oxygen species
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An effective negative pressure cavitation-microwave assisted extraction for determination of phenolic compounds in P. calliantha H. Andr.

2013

A novel negative pressure and microwave assisted extraction technique (NMAE) was first proposed and applied for extraction of phenolic compounds from pyrola. [C₄MIM]BF₄ aqueous solution was selected as extraction solvent. Optimal extraction conditions were microwave power 700 W, negative pressure -0.07 MPa, temperature 40 °C, liquid-solid ratio 20 : 1, ionic liquid (IL) concentration 0.5 M, extraction time 15 min. The predominance of NMAE was investigated by comparing with microwave-assisted extraction (MAE) and negative pressure cavitation extraction (NPCE) using a first-order kinetics equation. The C∞ values of the target compounds by NMAE were from 0.406 to 5.977 mg g⁻¹ higher than these…

ReproducibilityAqueous solutionChromatographyPlant ExtractsLiquid-Liquid ExtractionExtraction (chemistry)Analytical chemistryRepeatabilityBiochemistryAnalytical ChemistrySolventMatrix (chemical analysis)chemistry.chemical_compoundPhenolschemistryIonic liquidPressureElectrochemistryEnvironmental ChemistrySample preparationMicrowavesPyrolaChromatography High Pressure LiquidSpectroscopyThe Analyst
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Analysis of pesticide residues in fruit and vegetables by matrix solid phase dispersion (MSPD) and different gas chromatography element-selective det…

1995

A comparison between different element selective detectors for the determination of organophosphorus and organochlorine pesticide residues, from fruit and vegetables, was performed by capillary GC with electron capture detector (ECD), nitrogen phosphorus detector (NPD), flame photometric detector (FPD) in the sulphur and phosphorus modes, and mass spectrometry detector (MSD) in selected ion monitoring (SIM) mode. Pesticides were extracted from the different foodstuffs by Matrix Solid Phase Dispersion (MSPD). Recoveries of 41–108 % with relative standard deviation of 2–14 % in the concentration range 0.5–10 μg L−1 were obtained in oranges, lemons, grapefruit, pears, plums, lettuces and tomat…

Residue (complex analysis)ChromatographyNitrogen–phosphorus detectorPesticide residueChemistryOrganic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryAnalytical ChemistryMatrix (chemical analysis)Electron capture detectorSelected ion monitoringGas chromatographySolid phase extractionChromatographia
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Retention and release of taste and aroma compounds from the food matrix during mastication and ingestion

2016

This chapter gives an overview of the physicochemical and sensory properties of aroma and taste compounds from food, their interactions with the food matrix, and their release during food breakdown in the mouth. In order to be perceived by the taste or olfactory receptors, aroma and taste compounds have first to be released in the saliva, which depends on the food matrix composition and structure, and on the masticatory behavior. Aroma compounds have then to be transported from the oral to the nasal cavity. Different mechanistic models have been developed to understand better aroma and taste compounds release in function of both food and individual, however, they are still not able to predi…

SalivaTasteMatrix compositionbiologyChemistry[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritiondigestive oral and skin physiologyfood and beveragesSensory systembiology.organism_classificationMatrix (chemical analysis)IngestionFood science[SDV.AEN]Life Sciences [q-bio]/Food and NutritionMasticationAroma
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Kinetics of particle growth and particle composition of a commercial Al-Li alloy by means of small-angle scattering

1991

Abstract Extending previous work done on a similar alloy, small-angle X-ray scattering measurements are reported for a commercial Al-Cu-Li alloy (2–68% Cu and 1–88% Li by weight). Data have been analysed by means of an ellipsoidal model of precipitate particles using a method previously proposed by some of us which, incorporating interparticle interference effects, reproduces the fuli scattering intensities of the samples studied. Particie dimensions obtained from the fit indicate that the Lifshitz-Slyozov coarsening mechanism holds for ageing at higher temperatures and longer times. The activation energy for volume diffusivity obtained is similar to that of pure binary alloys. The scatteri…

ScatteringGeneral Chemical EngineeringAlloyGeneral Physics and Astronomychemistry.chemical_elementThermodynamicsActivation energyengineering.materialThermal diffusivityMatrix (chemical analysis)CrystallographyVolume (thermodynamics)chemistryengineeringLithiumSmall-angle scattering
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From the Beehives: Identification and Comparison of Physicochemical Properties of Algerian Honey

2021

In this study, the authors aimed at characterizing 11 Algerian kinds of honey taken from various geographical locations (beehives located at Djelfa (Medjbara and Dzaira), Laghouat, Aflou, Medea, Tiaret, Sidi bel-Abbes, Tiaret, Ain-Safra, Mostaganem, El Bayadh, and Ghardïa). The authors investigated the physicochemical parameters of these honey samples, including density, water content, electrical conductivity, ash content, pH, hydroxymethylfurfural (HMF) content, free acidity, and color. The physicochemical parameters obtained were found to be within acceptable ranges according to the international standards (Codex Alimentarius) for 9 out of 11 analyzed samples: density 1.38–1.50 g/cm3 (the…

SciencefoodQphysicochemical parametershydroxymethylfurfuralhoneyManagement Monitoring Policy and LawHoney sampleschemistry.chemical_compoundchemistryqualityAlgeriaFood scienceWater contentHydroxymethylfurfuralphysicochemical analysisNature and Landscape ConservationResources
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Physiological HEPES Buffer Proposed as a Calibrator for pH Measurement in Human Blood

1999

Abstract N-(2-hydroxyethyl)-piperazine-N'-2-ethanesulfonic acid, known as HEPES buffer, with p K in the physiological range was studied for use as an alternative to conventional phosphate buffer for the calibration of pH in modern clinical analyzers. In different series of aqueous equimolar HEPES buffer, pH was measured at 37 °C with a capillary glass electrode standardized previously using phosphate, and variations due to changes in total HEPES buffer concentration (0.025 to 0.320 mol/l), and NaCl (0 to 0.250 mol/l) were monitored. For 0.05 equimolar HEPES buffer without NaCl, the pH of 7.362 ± 0.003 (n = 15) obtained coincided well with the reference pH (7.364) from the National Institute…

SodiumClinical BiochemistryAnalytical chemistrySalt (chemistry)chemistry.chemical_elementBuffersSodium ChlorideBuffer (optical fiber)law.inventionchemistry.chemical_compoundlawProhibitinsHumansHEPESchemistry.chemical_classificationAqueous solutionChromatographyBiochemistry (medical)General MedicineBuffer solutionHydrogen-Ion ConcentrationPhosphateGlass electrodechemistryCalibrationHEPESBlood Chemical Analysiscclm
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Determination of organophosphate flame retardants in soil and fish using ultrasound-assisted extraction, solid-phase clean-up, and liquid chromatogra…

2017

A solid–liquid extraction method in combination with high‐performance liquid chromatography and tandem mass spectrometry was developed and optimized for extraction and analysis of organophosphorus flame retardants in soil and fish. Methanol was chosen as the optimum extraction solvent, not only in terms of extraction efficiency, but also for its broader analyte coverage. The subsequent clean‐up by solid‐phase extraction is required to eliminate matrix coextractives and reduce matrix effects. Recoveries of the optimized method were 50–121% for soil and 47–123% for biota, both with high precision (RSDs <12% in soil and <23% in biota). The method limits of detection ranged from 0.06 to 0.20 ng…

Solid–liquid extractionFood ContaminationFiltration and SeparationLiquid chromatography with tandem mass spectrometry010501 environmental sciencesMass spectrometry01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)SoilTandem Mass SpectrometryAnimalsSoil PollutantsSolid phase extractionChromatography High Pressure LiquidFlame Retardants0105 earth and related environmental sciencesDetection limitChromatographyChemistrySolid Phase Extraction010401 analytical chemistryExtraction (chemistry)FishesSoil classificationSoil contaminationOrganophosphates0104 chemical sciencesFishSeafoodOrganophosphorus flame retardantsJournal of Separation Science
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A statistical design of experiments for optimizing the MALDI-TOF-MS sample preparation of polymers. An application in the assessment of the thermo-me…

2011

[EN] The sample preparation procedure for MALDI-TOF MS of polymers is addressed in this study by the application of a statistical Design of Experiments (DoE). Industrial poly (ethylene terephthalate) (PET) was chosen as model polymer. Different experimental settings (levels) for matrixes, analyte/matrix proportions and concentrations of cationization agent were considered. The quality parameters used for the analysis were signal-to-noise ratio and resolution. A closer inspection of the statistical results provided the study not only with the best combination of factors for the MALDI sample preparation, but also with a better understanding of the influence of the different factors, individua…

Solucions polimèriquesEthylenePolymersAnalytical chemistryDegradation kineticsBiochemistryThermo-mechanical degradationSample preparation procedureAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundDegradationGlycolsMatrix assisted laser desorption ionization time of flight mass spectrometryPolyethylene terephthalateMechanismsCationizationSample preparationRecyclingMechanical recyclingSpectroscopyPriority journalchemistry.chemical_classificationDithranolSignal to noise ratioPolyethylene terephthalateHydrolysisMultiple processingPolymerPoly (ethylene terephthalate)Potential reactionsInjection cyclesMAQUINAS Y MOTORES TERMICOSInductively coupled plasmaSimulationEthersMatrix-assisted laser desorption/ionization time-of-flightQuality parametersDesign of ExperimentsGlycol unitsSample preparationArticleEthyleneEnvironmental ChemistryPolyethylene terephthalatesMALDI TOF MSSignal noise ratioMass spectrometryMatrixTermoplàsticsSignal to noiseTransesterificationDegradation mechanismMatrix-assisted laser desorption/ionizationStatistical design of experimentsTransesterificationchemistryChemical engineeringOligomersDesorptionEthylene glycolControlled studyProcess optimizationAnalytica chimica acta
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