Search results for " standard deviation"

showing 10 items of 79 documents

A multi-model assessment of the impact of sea spray geoengineering on cloud droplet number

2012

Artificially increasing the albedo of marine boundary layer clouds by the mechanical emission of sea spray aerosol has been proposed as a geoengineering technique to slow the warming caused by anthropogenic greenhouse gases. A previous global model study (Korhonen et al., 2010) found that only modest increases (< 20%) and sometimes even decreases in cloud drop number (CDN) concentrations would result from emission scenarios calculated using a windspeed dependent geoengineering flux parameterisation. Here we extend that work to examine the conditions under which decreases in CDN can occur, and use three independent global models to quantify maximum achievable CDN changes. We find that dec…

Atmospheric ScienceMeteorologybusiness.industryCloud coverDrop (liquid)Atmospheric sciencesSea spraylcsh:QC1-999Aerosollcsh:Chemistrylcsh:QD1-999Greenhouse gasGeometric standard deviationEnvironmental scienceGeoengineeringParticle sizebusinesslcsh:Physics
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Calcifying phytoplankton standing stocks in the North Pacific from the R/V Kilo Moana cruise KM1712

2022

This dataset compiles the CaCO3 standing stocks of living coccolithophores (mg/m³), of detached coccoliths (mg/m³) and the integrated CaCO3 standing stocks of coccolithophores (mg/m²). The samples were collected in the North Pacific between Hawaii and the Gulf of Alaska during the R/V Kilo Moana cruise KM1712 in August 2017, with rosette Niskin bottles equiped with CTD (Sea-Bird SBE 9) at different depths throughout the photic zone including the deep chlorophyll maximum. To estimate the CaCO3 contribution by coccolithophore assemblages in each sample, we carried out the transformation of coccospheres in number of coccoliths, following the estimates by Yang and Wei (2003), and then we adopte…

Carbonate productionLongitude of eventCoccosphaerales calcium carbonate per area standard deviationwaterRV Kilo MoanaCTD/RosetteLatitude of eventBottle numberKM1712Coccosphaerales calcium carbonate per areaDate/Time of eventCalculatedCoccolithophorespteropodsNorth Pacificcalcium carbonate per volumeDEPTH waterEvent labelDate Time of eventforaminiferaCTD Rosettecalcium carbonate per areaCoccosphaeralesDEPTHStanding stocksEarth System ResearchHeteropodsCoccosphaerales calcium carbonate per volumestandard deviationStation label
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Immobilization of reagents by polymeric materials. Determination of metamizol

1992

Abstract A method for immobilization of inorganic reagents, based on the dispersion of the reagent into an unsaturated polyester solution is applied to immobilization of lead dioxide. The obtained solid is of application in a flow-injection manifold for indirect atomic absorption determination of metamizol in pharmaceutical formulations. The procedure gives a linear calibration graph up to 6 ppm of metamizol with a relative standard deviation of 1.6% (3.0 mg/l) and a sample throughput of 72 hr−1.

ChromatographyCalibration curveChemistryRelative standard deviationUnsaturated polyesterLead dioxideAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawReagentAtomic absorption spectroscopyDispersion (chemistry)Nuclear chemistryTalanta
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Determination of trichothecenes in chicken liver using gas chromatography coupled with triple-quadrupole mass spectrometry

2018

Abstract Chicken meat and edible offal are included in a wide number of preparations in the worldwide cuisine. Among the offal, the liver is one of the most consumed in some countries like Egypt since it is rich in proteins and is an economical source of many essential nutrients for humans. Mycotoxins, secondary toxic metabolites produced by fungi, have the potential to enter human food chain not only with cereal consumption but also through edible tissues from animals fed with mycotoxin-contaminated feed. Accordingly, a rapid method for the determination of eight trichothecenes in chicken liver was developed based on a quick, easy, cheap, effective, rugged and safe (QuEChERS) extraction an…

ChromatographyChemistryExtraction (chemistry)Relative standard deviation04 agricultural and veterinary sciencesQuechersTandem mass spectrometry040401 food sciencechemistry.chemical_compound0404 agricultural biotechnologyChicken LiverTriple quadrupole mass spectrometryGas chromatographyMycotoxinFood ScienceLWT
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Target analysis of primary aromatic amines combined with a comprehensive screening of migrating substances in kitchen utensils by liquid chromatograp…

2015

An analytical strategy including both the quantitative target analysis of 8 regulated primary aromatic amines (PAAs), as well as a comprehensive post-run target screening of 77 migrating substances, was developed for nylon utensils, using liquid chromatography-orbitrap-high resolution mass spectrometry (LC-HRMS) operating in full scan mode. The accurate mass data were acquired with a resolving power of 50,000 FWHM (scan speed, 2 Hz), and by alternating two acquisition events, ESI+ with and without fragmentation. The target method was validated after statistical optimization of the main ionization and fragmentation parameters. The quantitative method presented appropriate performance to be u…

ChromatographyPrimary (chemistry)Food contactChemistryRelative standard deviationAnalytical chemistryTarget analysisFood ContaminationOrbitrapCooking and Eating UtensilsAnalytical Chemistrylaw.inventionMassNylonsKitchen utensilslawTandem Mass SpectrometryAnalytical strategyHumansAminesOrganic ChemicalsChromatography LiquidTalanta
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FIA-Chemiluminescence Determination of Acridine Yellow

2003

Abstract The direct determination of yellow acridine is performed by a FIA assembly on the basis of the oxidation of the acridine. The acridine solution is injected into a pure water stream. This solution merges with the oxidant solution (KMnO4 in sulfuric acid medium) and the resulting chemiluminescence allows the method to be applied over the range 0.01–100 mg L−1 of acridine with a correlation coefficient of 0.9997. The relative standard deviation (%) is 1.6 and the sample throughput 60 h−1. The influence of foreign substances is also tested. The new method is applied to the determination of yellow acridine in waste waters.

ChromatographyStereochemistryBiochemistry (medical)Clinical BiochemistryRelative standard deviationSulfuric acidWater streamBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistryAcridine yellowlawAcridineElectrochemistryQuantitative analysis (chemistry)SpectroscopyChemiluminescenceAnalytical Letters
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Comparison of spectrophotometric and HPLC methods for determining sialic acid in infant formulas

2011

Abstract Two methods for determining sialic acid in infant formulas – spectrophotometry and HPLC with fluorescence detection – have been optimised and validated, the first one allows to determine total sialic acid while the second allows to differentiate the two main forms of sialic acid (N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc)). A common sample preparation procedure (hydrolysis and purification) for both methods has been proposed. The linearity (from 6 to 150 μg of total sialic acid in the assay for spectrophotometry, and from 12.5 to 250 ng and 1 to 5 ng of Neu5Ac and Neu5Gc, respectively, for HPLC) is adequate. The detection and quantification limits (0.29…

Chromatographymedicine.diagnostic_testRelative standard deviationGeneral MedicineHigh-performance liquid chromatographyFluorescenceAnalytical ChemistrySialic acidHydrolysischemistry.chemical_compoundInfant formulachemistrySpectrophotometrymedicineSample preparationFood ScienceFood Chemistry
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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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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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