Search results for "Detection limit"

showing 10 items of 810 documents

2017

Abstract. Hydroxyl (OH) radical reactivity (kOH) has been measured for 18 years with different measurement techniques. In order to compare the performances of instruments deployed in the field, two campaigns were conducted performing experiments in the atmospheric simulation chamber SAPHIR at Forschungszentrum Jülich in October 2015 and April 2016. Chemical conditions were chosen either to be representative of the atmosphere or to test potential limitations of instruments. All types of instruments that are currently used for atmospheric measurements were used in one of the two campaigns. The results of these campaigns demonstrate that OH reactivity can be accurately measured for a wide rang…

Detection limitAtmospheric Science010504 meteorology & atmospheric sciencesChemistryAnalytical chemistry010501 environmental sciences01 natural sciencesAtmospheric simulationAtmosphereAtmospheric measurements13. Climate actionReactivity (chemistry)Nitrogen oxides0105 earth and related environmental sciencesAtmospheric Measurement Techniques
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Determination of n-alkanes, polycyclic aromatic hydrocarbons and hopanes in atmospheric aerosol: evaluation and comparison of thermal desorption GC-M…

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…

Detection limitAtmospheric Science010504 meteorology & atmospheric sciencesCorrelation coefficientlcsh:TA715-787Chemistrylcsh:Earthwork. FoundationsThermal desorptionCoal combustion productsFraction (chemistry)Repeatability010501 environmental sciences01 natural scienceslcsh:Environmental engineeringAerosolEnvironmental chemistrylcsh:TA170-171Gas chromatography–mass spectrometry0105 earth and related environmental sciencesAtmospheric Measurement Techniques
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Bromine speciation in volcanic plumes: new in situ derivatization LC-MS method for the determination of gaseous hydrogen bromide by gas diffusion den…

2020

The chemical characterization of volcanic gas emissions gives insights into the interior of volcanoes. Monitoring of BrO/SO2-ratios has recently been correlated with changes in the activity of a volcano. BrO and SO2 can both be measured autonomously and simultaneously with the same instruments from a safe distance, making their ratio potentially a strong monitoring tool. However, BrO is not a primary emitted volcanic volatile and there exist still uncertainties about the formation of BrO in volcanic plumes, mostly due to the lack of analytical approaches for the accurate speciation of certain key compounds. This study describes a new method for the determination of the BrO precursor, the ga…

Detection limitAtmospheric ScienceBromine010504 meteorology & atmospheric sciencesElectrospray ionizationDiffusionTA715-787Analytical chemistrychemistry.chemical_elementEnvironmental engineeringTA170-17101 natural sciencesPlumechemistry.chemical_compoundchemistryEarthwork. FoundationsBromideGaseous diffusionDerivatization0105 earth and related environmental sciences
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2009

Abstract. Systematic laboratory experiments were performed to investigate quantification of various species with two versions of the Aerodyne Aerosol Mass Spectrometer, a Quadrupole Aerosol Mass Spectrometer (Q-AMS) and a compact Time-of-Flight Aerosol Mass Spectrometer (c-ToF-AMS). Here we present a new method to continuously determine the detection limits of the AMS analyzers during regular measurements, yielding detection limit (DL) information under various measurement conditions. Minimum detection limits range from 0.03 μg m−3 (nitrate, sulfate, and chloride) up to 0.5 μg m−3 (organics) for the Q-AMS. Those of the c-ToF-AMS are found between 0.003 μg m−3 (nitrate, sulfate) and 0.03 μg …

Detection limitAtmospheric Sciencechemistry.chemical_compoundNitratechemistryAnalytical chemistryMass concentration (chemistry)SulfateContaminationMass spectrometryAerosolIonAtmospheric Measurement Techniques
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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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Silver based sensors from CD for chloride ions detection

2021

This preliminary work shows a new and innovative way to produce silver based electrodes from compact discs and its application towards the detection of chloride ions. A complete sensor was obtained from the compact discs with working, reference and counter electrode made of silver. Chloride ions were detected by exploiting the high affinity of silver with this anion to produce silver chloride. This electrochemical oxidation of silver can be monitored by using an electrochemical technique such as linear scan voltammetry. Indeed, during linear scan voltammetry the oxidation of silver to silver chloride lead to a peak current that increases linearly with chloride concentration. Using this tech…

Detection limitAuxiliary electrodevoltammetryMaterials scienceInorganic chemistrycircular economyelectrochemical sensorElectrochemistryChloride ions electrochemical sensor voltammetry circular economyChlorideIonSilver chloridechemistry.chemical_compoundchemistryElectrodemedicineChloride ionsVoltammetrymedicine.drug
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Bioanalysis of digoxin and its metabolites using direct serum injection combined with liquid chromatography and on-line immunochemical detection.

1994

Abstract An automated dual-column liquid chromatographic assay for digoxin is described. Serum samples are directly injected onto a restricted-access solid-phase extraction support. After liquid chromatographic (LC) separation on a C18 analytical column, antigenic analytes are detected by means of post-column immunochemical detection (ICD) using fluorescein-labelled antibodies against digoxigenin. The detection limit of this assay is 160 pg/ml (preconcentration of 1.0 ml serum). With the present method digoxin and three of its cross-reactive metabolites were determined in serum taken from patients which were orally administered a 1-mg dose of digoxin. The results obtained with LC—ICD were c…

Detection limitBioanalysisAnalyteDigoxinChromatographyDigoxinmedicine.diagnostic_testMetaboliteImmunochemistryFluoroimmunoassayGeneral ChemistryCross Reactionschemistry.chemical_compoundchemistryImmunoassaymedicineDigoxigeninHumansQuantitative analysis (chemistry)DigoxigeninBiomarkersChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical applications
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Immunochromatographic Assay for Quantitation of Milk Progesterone.

1996

We describe a rapid immunochromatographic method for the quantitation of progesterone in bovine milk. The method is based on a 'competitive' assay format using the monoclonal antibody to progesterone and a progesterone-protein conjugate labelled with colloidal gold particles. The monoclonal antibody to progesterone is immobilized as a narrow detection zone on a porous membrane. The sample is mixed with colloidal gold particles coated with progesterone-protein conjugate, and the mixture is allowed to migrate past the detection zone. Migration is facilitated by capillary forces. The amount of labelled progesterone-protein conjugate bound to the detection zone, as detected by photometric scann…

Detection limitBovine milkChromatographymedicine.drug_classCapillary actionChemistryGeneral Chemical EngineeringAntibodies MonoclonalCross ReactionsMonoclonal antibodySensitivity and SpecificityChromatography AffinityMilkColloidal goldPorous membranemedicineAnimalsCattleChromatography Thin LayerProgesteroneConjugateActa Chemica Scandinavica
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The volatile inventory (F, Cl, Br, S, C) of magmatic apatite: An integrated analytical approach

2012

Abstract Apatite is ubiquitous in a wide range of magmatic rocks and its F–Cl–Br–S systematics can be used to decipher e.g., mixing processes within a magmatic complex and may give insights into fluid un-mixing and degassing processes during the emplacement and cooling of plutonic rocks. In this study, we analyzed a F-apatite (Durango, Mexico), a Cl-apatite (Odegarden, Norway) and apatites from five plutonic samples from the alkaline Mt. Saint Hilaire Complex (Canada) by means of Electron Microprobe Analysis (EPMA), Laser Ablation ICP-MS (LA-ICP-MS), Secondary Ion Mass Spectrometry (SIMS), pyrohydrolysis combined with ion chromatography, Fourier Transformed Infrared Spectroscopy (FTIR), Ins…

Detection limitBromineChemistryAnalytical chemistryInfrared spectroscopychemistry.chemical_elementGeologyElectron microprobeApatiteSecondary ion mass spectrometryGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumFourier transform infrared spectroscopyNeutron activation analysisChemical Geology
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Flow injection spectrophotometric determination of boron in ceramic materials.

1998

Abstract A flow injection spectrophotometric method for the determination of boron in ceramic materials is described. The method is based on spectrophotometric measurement of the decrease in the pH produced by the reaction between boric acid and mannitol in the presence of an acid-base indicator. A bichannel FI (flow injection) manifold in which the sample solutions were injected into deionized water (at pH 5.4) and the stream was later merged with the reagent stream (a mannitol solution containing 1×10 −4 mol l −1 bromocresol green at pH 5.4), was used. Transient signals were monitored at 616 nm. A theoretical model which describes the dependence between the absorbance values and boric aci…

Detection limitBromocresol greenmedicine.diagnostic_testPotentiometric titrationAnalytical chemistrychemistry.chemical_elementCeramic materialsAnalytical ChemistryBoric acidAbsorbancechemistry.chemical_compoundchemistrySpectrophotometryReagentmedicineBoronTalanta
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