Search results for "Chemical ionization"

showing 10 items of 65 documents

Aerosol Chemistry Resolved by Mass Spectrometry: Linking Field Measurements of Cloud Condensation Nuclei Activity to Organic Aerosol Composition.

2016

Aerosol hygroscopic properties were linked to its chemical composition by using complementary online mass spectrometric techniques in a comprehensive chemical characterization study at a rural mountaintop station in central Germany in August 2012. In particular, atmospheric pressure chemical ionization mass spectrometry ((-)APCI-MS) provided measurements of organic acids, organosulfates, and nitrooxy-organosulfates in the particle phase at 1 min time resolution. Offline analysis of filter samples enabled us to determine the molecular composition of signals appearing in the online (-)APCI-MS spectra. Aerosol mass spectrometry (AMS) provided quantitative measurements of total submicrometer or…

010504 meteorology & atmospheric sciencesAnalytical chemistryAtmospheric-pressure chemical ionizationGeneral Chemistry010501 environmental sciencesMass spectrometry01 natural sciencesAerosolchemistry.chemical_compoundchemistryEnvironmental ChemistryAerosol mass spectrometryCloud condensation nucleiSulfateChemical compositionMass fraction0105 earth and related environmental sciencesEnvironmental sciencetechnology
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Aerosol Chemistry Resolved by Mass Spectrometry: Insights into Particle Growth after Ambient New Particle Formation

2016

Atmospheric oxidation of volatile organic compounds (VOCs) yields a large number of different organic molecules which comprise a wide range of volatility. Depending on their volatility, they can be involved in new particle formation and particle growth, thus affecting the number concentration of cloud condensation nuclei in the atmosphere. Here, we identified oxidation products of VOCs in the particle phase during a field study at a rural mountaintop station in central Germany. We used atmospheric pressure chemical ionization mass spectrometry ((-)APCI-MS) and aerosol mass spectrometry for time-resolved measurements of organic species and of the total organic aerosol (OA) mass in the size r…

010504 meteorology & atmospheric sciencesChemistryElectrospray ionizationAnalytical chemistryAtmospheric-pressure chemical ionizationGeneral Chemistry010501 environmental sciencesMass spectrometry01 natural sciencesAerosolParticle growthEnvironmental ChemistryCloud condensation nucleiAerosol mass spectrometryVolatility (chemistry)0105 earth and related environmental sciencesEnvironmental Science & Technology
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Formation of 3-methyl-1,2,3-butanetricarboxylic acid via gas phase oxidation of pinonic acid – a mass spectrometric study of SOA aging

2012

Abstract. This paper presents the results of mass spectrometric investigations of the OH-initiated oxidative aging of α-pinene SOA under simulated tropospheric conditions at the large aerosol chamber facility AIDA, Karlsruhe Institute of Technology. In particular, the OH-initiated oxidation of pure pinic and pinonic acid, two well-known oxidation products of α-pinene, was investigated. Two complementary analytical techniques were used, on-line atmospheric pressure chemical ionization/mass spectrometry (APCI/MS) and filter sampling followed by liquid chromatography/mass spectrometry (LC/ESI-MS). The results show that 3-methyl-1,2,3-butanetricarboxylic acid (MBTCA), a very low volatile α-pine…

540 Chemistry and allied sciencesAtmospheric ScienceChromatographyChemistryAtmospheric-pressure chemical ionizationFraction (chemistry)Mass spectrometryMass spectrometriclcsh:QC1-999JGas phaseAerosollcsh:ChemistryAcid oxidationlcsh:QD1-999540 ChemieYield (chemistry)ddc:550lcsh:PhysicsAtmospheric Chemistry and Physics
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Determination of four parabens and bisphenols A, F and S in human breast milk using QuEChERS and liquid chromatography coupled to mass spectrometry

2018

Abstract For the first time, a multiresidue, sensitive and high throughput method for determination of bisphenol A, F and S and 4 parabens (methyl paraben, ethyl paraben, propyl paraben and butyl paraben) in human breast milk was developed. The proposed method includes an extraction and clean-up procedure based on QuEChERS methodology followed by liquid chromatography coupled to triple quadrupole mass spectrometry determination. Negative atmospheric pressure chemical ionization in the selected reaction monitoring mode was used for mass detection. During the method validation the recoveries varied between 83 and 115% with a precision lower than 20% for all analytes using spiked levels from 0…

AdultAnalyteBisphenol AClinical BiochemistryParabensAtmospheric-pressure chemical ionizationMass spectrometryQuechers030226 pharmacology & pharmacy01 natural sciencesBiochemistryMass SpectrometryAnalytical Chemistry03 medical and health scienceschemistry.chemical_compound0302 clinical medicinePhenolsLimit of DetectionLiquid chromatography–mass spectrometryHumansSulfonesBenzhydryl CompoundsChromatographyMilk HumanChemistry010401 analytical chemistrySelected reaction monitoringReproducibility of ResultsCell BiologyGeneral Medicine0104 chemical sciencesParabenLinear ModelsFemaleChromatography LiquidJournal of Chromatography B
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Identification of organic hydroperoxides and hydroperoxy acids in secondary organic aerosol formed during the ozonolysis of different monoterpenes an…

2009

On-line ion trap mass spectrometry (ITMS) enables the real-time characterization of reaction products of secondary organic aerosol (SOA). The analysis was conducted by directly introducing the aerosol particles into the ion source. Positive-ion chemical ionization at atmospheric pressure (APCI(+)) ITMS was used for the characterization of constituents of biogenic SOA produced in reaction-chamber experiments. APCI in the positive-ion mode usually enables the detection of [M+H](+) ions of the individual SOA components. In this paper the identification of organic peroxides from biogenic volatile organic compounds (VOCs) by on-line APCI-ITMS is presented. Organic peroxides containing a hydroper…

AerosolsOrganic peroxideChemical ionizationAir PollutantsSpectrometry Mass Electrospray IonizationOzonolysisAtmospheric pressureOrganic ChemistryAnalytical chemistryCarboxylic AcidsAtmospheric-pressure chemical ionizationHydrogen PeroxideOnline SystemsIon sourceAnalytical ChemistryPeroxideschemistry.chemical_compoundchemistryFunctional groupMonoterpenesPressureVolatilizationHydrogen peroxideSesquiterpenesSpectroscopyRapid communications in mass spectrometry : RCM
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Extraction and Sample Preparation

2015

As everyone knows, the role played by extraction and sample preparation in the analytical sciences cannot be overemphasized. Despite tremendous advances in chromatography, detection, and other aspects of analysis, extraction and sample preparation remain a preanalysis ritual of critical importance. It has been estimated that around 50% to 70% possibly even more of the time and effort that goes into an analytical process comprises extraction and sample preparation. Sample preparation procedure can vary in the degree of selectivity, speed, and convenience, depending on the approach and conditions used, as well as on the geometric configurations of the extraction phase and conditions. Proper d…

AnalyteBioanalysisChromatographylcsh:QD71-142Article SubjectChemistryElectrospray ionizationlcsh:Analytical chemistryAtmospheric-pressure chemical ionizationQuechersMass spectrometryBioinformaticsAnalytical ChemistryEditorialSample preparationSolid phase extractionInternational Journal of Analytical Chemistry
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Analysis of four parabens and bisphenols A, F, S in urine, using dilute and shoot and liquid chromatography coupled to mass spectrometry

2018

Abstract A new strategy for the analysis of 4 parabens (methylparaben, ethyl paraben, propyl paraben and butyl paraben) and 3 bisphenols (A, F and S) in human urine has been developed. Dilute and shoot and liquid chromatography coupled to mass spectrometry (LC-MS/MS) determination was employed. Procedural matched calibration, certified materials and spiked samples were used for validation. The obtained recoveries varied between 85 and 104% with a precision lower than 20% for all analytes. The LOQ was 0.20 ng mL for all analytes. Negative atmospheric pressure chemical ionization in the selected reaction monitoring mode was used for MS detection. The proposed method was successfully applied f…

AnalyteBisphenol AParabensAtmospheric-pressure chemical ionization02 engineering and technologyUrineMass spectrometry01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundPhenolsTandem Mass SpectrometryHumansSulfonesBenzhydryl CompoundsChromatographyMethylparaben010401 analytical chemistrySelected reaction monitoring021001 nanoscience & nanotechnology0104 chemical sciencesParabenchemistrySpain0210 nano-technologyChromatography LiquidTalanta
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Evaluation of analytical performance of gas chromatography coupled with atmospheric pressure chemical ionization Fourier transform ion cyclotron reso…

2019

Abstract A new analytical method was established and validated for the analysis of eighteen halogenated flame retardants (HFRs)in food products. Gas chromatography (GC) coupled to Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) employing atmospheric pressure chemical ionization (APCI) was used for the identification and quantitation of contaminants. Intra-laboratory validation of the method was performed with respect to recovery, repeatability, linear calibration ranges, instrumental and method limits of quantitation (i-LOQ and m-LOQ), and trueness was verified where possible by analysis of reference materials (RMs). The validation results indicated recoveries of ana…

AnalyteEnvironmental EngineeringMaterials scienceFood SafetyHalogenationHealth Toxicology and Mutagenesis0208 environmental biotechnologyAtmospheric-pressure chemical ionization02 engineering and technology010501 environmental sciences01 natural sciencesFourier transform ion cyclotron resonanceGas Chromatography-Mass SpectrometryMass SpectrometryCalibrationHalogenated Diphenyl EthersEnvironmental ChemistryHumans0105 earth and related environmental sciencesFlame RetardantsDetection limitChromatographyFourier AnalysisPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryRepeatabilityCyclotronsPollution020801 environmental engineeringFoodFood productsGas chromatographyFood AnalysisChemosphere
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High gas-phase mixing ratios of formic and acetic acid in the High Arctic

2018

Abstract. Formic and acetic acid are ubiquitous and abundant in the Earth's atmosphere and are important contributors to cloud water acidity, especially in remote regions. Their global sources are not well understood, as evidenced by the inability of models to reproduce the magnitude of measured mixing ratios, particularly at high northern latitudes. The scarcity of measurements at those latitudes is also a hindrance to understanding these acids and their sources. Here, we present ground-based gas-phase measurements of formic acid (FA) and acetic acid (AA) in the Canadian Arctic collected at 0.5 Hz with a high-resolution chemical ionization time-of-flight mass spectrometer using the iodide …

Atmospheric ScienceChemical ionization010504 meteorology & atmospheric sciencesChemical transport modelChemistryFormic acid010501 environmental sciences01 natural scienceslcsh:QC1-999lcsh:ChemistryAtmosphereAcetic acidchemistry.chemical_compoundOvercastlcsh:QD1-999ArcticReagentEnvironmental chemistrylcsh:Physics0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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Measurement of low-ppm mixing ratios of water vapor in the upper troposphere and lower stratosphere using chemical ionization mass spectrometry

2018

A chemical ionization mass spectrometer (CIMS) instrument has been developed for the fast, precise, and accurate measurement of water vapor (H2O) at low mixing ratios in the upper troposphere and lower stratosphere (UT/LS). A low-pressure flow of sample air passes through an ionization volume containing an α-particle radiation source, resulting in a cascade of ion-molecule reactions that produce hydronium ions (H3O+) from ambient H2O. The production of H3O+ ions from ambient H2O depends on pressure and flow through the ion source, which were tightly controlled in order to maintain the measurement sensitivity independent of changes in the airborne sampling environment. The instrument w…

Atmospheric ScienceChemical ionizationlcsh:TA715-787Chemistrylcsh:Earthwork. FoundationsAnalytical chemistryAtmosphärische SpurenstoffeWater vapourAtmospheric sciencesMass spectrometryIon sourcelcsh:Environmental engineeringTroposphereIonizationlcsh:TA170-171TropopauseStratosphereWater vapormass spectrometryAtmospheric Measurement Techniques
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