Search results for "deviation"

showing 10 items of 367 documents

Income Differences in Regions of Latvia – Problems and Challenges

2019

Income differences in regions of Latvia is becoming a greater problem for families as there are made decisions for emigration, for municipalities as there are significant reductions in tax (income and property) payers and for entrepreneurs as there are less customers for their products and services: those aspects are on great importance but not enough researched and discussed in academic research. Purpose of the study is to analyse income differences in the regions of Latvia. The tasks of the study: 1 to review theoretical background of income differences in context of regional development; 2 to review existing research of income differences in the regions in EU; 3 to analyse problems of in…

Descriptive statisticsincome differencesContext (language use)regional developmentLatviaStandard deviationEmigrationStandard errorGeographyHousehold income:SOCIAL SCIENCES::Business and economics [Research Subject Categories]Demographic economicsStatistical dispersionArithmetic mean
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Determination of tea tree oil terpenes by headspace gas chromatography mass spectrometry

2016

An alternative procedure was developed for determining quality control of terpenes in tea tree oil commercial samples. The method is based on static headspace gas chromatography mass spectrometry measurements. Absolute limits of detection ranged from 1 ng for p-cymene to 71 ng for terpinen-4-ol. The accuracy of the developed methodology was evaluated by comparing the obtained eucalyptol and terpinen-4-ol concentrations with those provided for a certified sample and by comparing the developed procedure with literature tea tree oil analysis methodology. In the same way, spiked commercial samples provided recovery values ranging between 94% and 100% for all the target analytes with relative st…

Detection limitAnalyteChromatography010405 organic chemistryChemistryGeneral Chemical Engineering010401 analytical chemistryRelative standard deviationGeneral EngineeringTea tree oilMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistryTerpenechemistry.chemical_compoundEucalyptolmedicineGas chromatographymedicine.drugAnalytical Methods
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Selection of calibration set samples in determination of olive oil acidity by partial least squares–attenuated total reflectance–Fourier transform in…

2003

Abstract A chemometric method has been applied for the determination of the free fatty acid (FFA) concentration in commercial olive oil samples of different types an origins by using Fourier transform infrared spectroscopy (FTIR) attenuated total reflectance (ATR) measurements. Different methods for selecting the training set, including hierarchical cluster analysis, were applied and compared. The prediction capabilities of partial least squares (PLS) multivariate calibration methods, net analyte signal (NAS) preprocessing followed by PLS or classical least squares (CLS) regression method of ATR–FTIR data were evaluated. Several aspects, like spectral range to be considered, different prepr…

Detection limitAnalyteMean squared errorChemistryAnalytical chemistryBiochemistryFourier transform spectroscopyStandard deviationAnalytical ChemistryChemometricsPartial least squares regressionCalibrationEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Improvement of the atomic fluorescence determination of mercury by using multicommutation

2002

Atomic fluorescence spectrometry (AFS) determination of Hg has been improved by exploiting the possibilities of the multicommutation approach in order to outline a fully mechanised system which supplies the same sensitivity as the use of continuous measurements, reducing drastically the reagents consumed and waste generation. The use of multicommutation with a simultaneous reduction of the liquid–gas separator volume and the insertion point modification of argon transport gas provides a sensitivity of the AFS measurements of 300 mV ng−1 ml (using a full scale of 1000 mV), a limit of detection (3 s) of 1.3 ng l−1 and relative standard deviation values below 0.1% for 10 independent measuremen…

Detection limitAtomic fluorescenceChromatographyArgonChemistryRelative standard deviationAnalytical chemistrychemistry.chemical_elementSeparator (oil production)Analytical ChemistryMercury (element)Waste generationReagentSpectroscopyJ. Anal. At. Spectrom.
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Preliminary Results on the Use of Leather Chrome Shavings for Air Passive Sampling

2012

A new passive sampler based on low-density polyethylene (LDPE) layflat tube filled with chrome shavings from tannery waste residues was evaluated to determine volatile organic compounds (VOCs) in indoor and outdoor areas. VOCs were directly determined by head space-gas chromatography-mass spectrometry (HS-GC-MS) without any pretreatment of the sampler and avoiding the use of solvents. Limit of detection values ranging from 20 to 75 ng sampler−1and good repeatability values were obtained for VOCs under study with relative standard deviation values from 2.8 to 9.6% except for carbon disulfide for which it was 22.5%. The effect of the amount of chrome shavings per sampler was studied and resul…

Detection limitCarbon disulfideMaterials sciencelcsh:QD71-142Article SubjectGeneral Chemical EngineeringRelative standard deviationlcsh:Analytical chemistryRepeatabilityPolyethylenePulp and paper industrycomplex mixturesComputer Science ApplicationsAnalytical ChemistryLow-density polyethylenechemistry.chemical_compoundAdsorptionchemistryInstrumentationPassive samplingResearch ArticleJournal of Analytical Methods in Chemistry
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Selective determination of clenbuterol residues in urine by molecular imprinted polymer—Ion mobility spectrometry

2017

Abstract Clenbuterol is banned for sports use and strictly regulated in livestock industry. In this study, a procedure for the determination of clenbuterol residues in water and urine has been developed using selective supports combined with ion mobility spectrometry (IMS) determination. A molecular imprinted polymer (MIP) was used for efficient clean-up and preconcentration of clenbuterol followed to a dispersive liquid-liquid microextraction (DLLME) in order to improve selectivity and sensitivity of IMS determinations. Quantitative recoveries from 81 to 99% were obtained for water and spiked urine samples using MIP-DLLME-IMS method. A precision of 4.5%, established as the relative standar…

Detection limitChromatographyChemistryIon-mobility spectrometry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymer02 engineering and technologyUrine021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryLiquid chromatography–mass spectrometryClenbuterolmedicine0210 nano-technologySpectroscopymedicine.drugMicrochemical Journal
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Die direkte quantitative auswertung von dünnschichtchromatogrammen durch remissions- und fluoreszenzmessungen

1971

Abstract Direct quantitative evaluation of thin-layer chromatograms by remission- and fluorescence measurements. Part 6. Determination of adrenaline, noradrenaline and dopamine from urine Adrenaline, noradrenalineand dopamine were separated from urine on aluminium oxide columns; after elution they were converted into ther O 3 ,O 4 ,N-triacetyl derivatives and separated using thin-layer chromatography. The triacetyl derivatives were in situ converted to fluorescing compounds using ethylene diamine and quantitatively estimated using the Chromatogram-Spectrophotometer (Carl Zeiss, Oberkochen). The advantage of this method over the conventional fluorometric determination of catecholamines in so…

Detection limitChromatographyEthylene diamineChemistryElutionOrganic ChemistryRelative standard deviationThin layerGeneral MedicineBiochemistryAnalytical ChemistryJournal of Chromatography A
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Fast extraction methodologies for the determination of toxic arsenic in meat

2017

Summary A nonchromatographic analytical procedure has been developed for the determination of arsenic in meat samples including the major toxic arsenic species arsenite, arsenate, monomethylarsonic acid (MMA) and dimetylarsinic acid (DMA). The method is based on the extraction of arsenic species in mild conditions, selective trivalent hydride formation and final determination by hydride generation atomic fluorescence spectroscopy (HG-AFS). Different extractant agents and two different procedures, microwave-assisted extraction (MAE) and ultrasound assisted extraction at room temperature, were evaluated for As species extraction. The method provided a limit of detection of 0.013 ng mL−1 and a…

Detection limitChromatographyHydride010401 analytical chemistryExtraction (chemistry)Relative standard deviationArsenatechemistry.chemical_elementMonomethylarsonic acid010501 environmental sciences01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental chemistryArsenic0105 earth and related environmental sciencesFood ScienceArseniteInternational Journal of Food Science & Technology
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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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Solid glucose biosensor integrated in a multi-well microplate coupled to a camera-based detector: Application to the multiple analysis of human serum…

2018

Abstract In the present work, a biosensor adapted in a 96-well microplate has been coupled with a smartphone-based photometer in order to develop a low-cost colorimetric multi-sample dispositive. The strength of this biosensing system is based on the integration of the biosensor into the 96-well microplate and the use of a smartphone and free image analysis software as a microplate reader. The performance of the proposed biosensor has been demonstrated to determine glucose in several human serum samples. This method is simple, cost-effective, sensitive and selective for the determination of glucose in serum, with detection limits of 1.8 mg/dL and a good linearity over the range 6–88 mg/dL. …

Detection limitChromatographyMaterials scienceDetectorRelative standard deviationMetals and Alloys02 engineering and technologyPhotometer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsSerum samples01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionMicroplate ReaderlawMaterials ChemistryElectrical and Electronic Engineering0210 nano-technologyInstrumentationBiosensorSensors and Actuators B: Chemical
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