Search results for "Detection limit"

showing 10 items of 810 documents

Development of a new method for the separation of vanadium species and chloride interference removal using modified silica capillaries-DIN-ICP-MS

2004

Abstract A new on-line method for the separation of vanadium (IV) and vanadium (V) as well as for the removal of ClO+ mass spectral interference on vanadium determination by quadrupole-ICP-MS has been developed. The sample introduction system consists of a modified fused silica capillary coupled to a direct injection nebuliser (DIN), between the solvent delivery system and the ICP. Fused silica capillaries were treated with different anion and cation exchanger reagents and were tested for the retention of Cl− and the separation of vanadium ions at μg l−1 levels. A suitable strong anion exchanger functional group (3-aminopropyltrimethoxy silane) was selected. Chlorine anions were retained in…

Detection limitIon exchangeAnalytical chemistrychemistry.chemical_elementVanadiumChlorideAnalytical ChemistrySolventchemistryReagentChlorinemedicineInductively coupled plasma mass spectrometrySpectroscopymedicine.drugMicrochemical Journal
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Development of an ICP-IDMS method for accurate routine analyses of toxic heavy metals in polyolefins and comparison with results by TI-IDMS

2000

An inductively coupled plasma isotope dilution mass spectrometric (ICP-IDMS) method was developed as a suitable method - with respect to its sensitivity, precision, accuracy, and time-consumption - for the analysis of toxic heavy metal traces (Pb, Cd, Cr, and Hg) in polyolefins. Results for Pb, Cd, and Cr were compared with those obtained by thermal ionization isotope dilution mass spectrometry (TI-IDMS), which was used as a reference method. Because of its high first ionization potential and its high volatility mercury could not be determined by TI-IDMS. A multi-element spike solution, containing isotopically enriched 206Pb, 116Cd, 53Cr, and 201Hg, was used for the isotope dilution step. D…

Detection limitIsotopeChemistryAnalytical chemistryThermal ionizationchemistry.chemical_elementAlkenesIsotope dilutionMass spectrometrySensitivity and SpecificityBiochemistryHazardous SubstancesMass SpectrometryMercury (element)IsotopesPolyethyleneMetals HeavyInductively coupled plasmaChemical decompositionFresenius' Journal of Analytical Chemistry
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Trace analysis of plutonium in environmental samples by resonance ionization mass spectroscopy (RIMS)

1998

Resonance ionization mass spectroscopy (RIMS) is well suited for trace analysis of long-lived radioisotopes in environmental, biological and technical samples. By multiple resonant laser excitation and ionization of the elemental atoms under investigation, an extremely high element selectivity can be achieved. In addition, isotope selectivity is obtained by subsequent mass analysis. The excellent sensitivity results from the large atomic cross-sections in the excitation–ionization process and the good detection efficiency for ions. The element selectivity of RIMS allows a simplified procedure for the chemical preparation of the samples compared to the requirements of thin sources for α-spec…

Detection limitIsotopeChemistryMechanical EngineeringMetals and AlloysAnalytical chemistrychemistry.chemical_elementMass spectrometryIonPlutoniumMechanics of MaterialsIonizationMaterials ChemistryPhysics::Atomic PhysicsTransuranium elementExcitationJournal of Alloys and Compounds
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Ultratrace analysis and isotope ratio measurements of long-lived radioisotopes by resonance ionization mass spectrometry (RIMS).

2003

Resonance Ionization Mass Spectrometry (RIMS) is a sensitive and selective method for ultratrace analysis of long-lived radioisotopes and isotope ratio measurements. It provides extremely high isobaric suppression and good overall efficiency. The experimental limits of detection are as low as 10(6) atoms per sample and isotopic selectivities of 5x10(12) have been obtained. The widespread potential of RIMS, using different experimental arrangements, is demonstrated for the determination of the radiotoxic isotopes Pu-238 to Pu-244 and Sr-89/Sr-90 in various environmental samples as well as for Ca-41 in nuclear reactor components and biomedical samples.

Detection limitIsotopeChemistryRadiochemistryAnalytical chemistryIsobaric processPlutonium-244Thermal ionization mass spectrometryMass spectrometryBiochemistryStrontium-90Analytical ChemistryPlutonium-238Analytical and bioanalytical chemistry
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Resonance ionization mass spectrometry for ultratrace analysis of plutonium with a new solid state laser system

2004

Abstract Resonance ionization mass spectrometry (RIMS) is well-suited for isotope selective ultratrace analysis of long-lived radioactive isotopes due to its high element and isotope selectivity and good sensitivity. For the analysis of plutonium with a pulsed RIMS apparatus, a powerful, reliable and easy to handle Nd:YAG pumped titanium–sapphire laser system has been developed and combined with a time-of-flight mass spectrometer. Spectroscopic measurements led to an efficient three step excitation and ionization scheme for plutonium with λ1 = 420.76 nm, λ2 = 847.28 nm, and λ3 = 767.53 nm. The isotope shifts in this scheme for the plutonium isotopes 238 Pu through 244 Pu have been determine…

Detection limitIsotopeChemistryRadiochemistryAnalytical chemistrychemistry.chemical_elementThermal ionization mass spectrometryCondensed Matter PhysicsLaserMass spectrometrylaw.inventionPlutoniumSolid-state laserlawIonizationPhysical and Theoretical ChemistryInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Recent developments in isotope ratio measurements by resonance ionization mass spectrometry

2005

Resonance ionization mass spectrometry (RIMS) has become a sensitive and highly selective technique for the determination of extremely low elemental or isotopic abundances, involving isotope ratio measurements with dynamical ranges of 109 and beyond. The experimental detection limits are as low as 106 atoms per sample, and isotopic selectivities of up to 1013 have been achieved under optimal conditions. The potential of RIMS using different experimental systems is outlined in the determination of lowest abundances and isotope ratios of long-lived radioisotopes of general importance like Pu238–244, 41Ca, and 236U for studies in geosciences, environmental, bio-medical or fundamental research.

Detection limitIsotopeChemistryStable isotope ratioResonance ionizationAnalytical chemistryPhysical and Theoretical ChemistryThermal ionization mass spectrometryCondensed Matter PhysicsMass spectrometryHighly selectiveInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Optimization of sample preparation conditions for detecting trace amounts of β-tegafur in α- and β-tegafur mixture.

2012

We report a semiquantitative method for determining trace amounts (<1%) of thermodynamically stable forms in polymorphic mixtures, focusing on sample preparation ef- fects on solid phase transitions. Tegafur (5-fluoro-1-(oxolan-2-yl)-1,2,3,4-tetrahydropyrimidine- 2,4-dione) was used as a model material in this study. The amounts of the thermodynamically stable $ tegafur were increased to levels detectable by powder X-ray diffractometry by grind- ing the samples in a ball mill in the presence of water. The limit of detection for this method was as low as 0.0005% of $ tegafur in " and $ tegafur mixtures. The amount of $ tegafur after sample preparation was found to be proportional to the init…

Detection limitLangmuirAntimetabolites AntineoplasticTrace AmountsChemistryAnalytical chemistryPharmaceutical ScienceTegafurPhase TransitionPolymorphism (materials science)IsomerismX-Ray DiffractionLimit of DetectionmedicineThermodynamicsSample preparationBall millMass fractionPowder Diffractionmedicine.drugTegafurJournal of pharmaceutical sciences
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Multi-element trace determinations in pure alkaline earth fluoride powders by high-resolution ICP-MS using wet-chemical sample preparation and laser …

2003

Four alternative analytical procedures for the determination of ten important trace impurities (Mg, Cr, Fe, Cu, Zn, Sr, Zr, Cd, Ba, and Pb) in pure alkaline earth fluoride powders were applied using high-resolution inductively coupled plasma mass spectrometry (ICP-MS). Two procedures are based on a wet-chemical microwave digestion with boric acid and quantification by the standard addition technique and isotope dilution mass spectrometry (IDMS), respectively. In addition, analyses are also performed by laser ablation as a direct solid sampling technique applying matrix-matched external calibration as well as isotope dilution of the powdered sample. For most elements good agreement between t…

Detection limitLaser ablationChemistryStandard additionAnalytical chemistryAnalytical proceduresSample preparationIsotope dilutionMicrowave digestionBiochemistryInductively coupled plasma mass spectrometryAnalytical ChemistryAnalytical and bioanalytical chemistry
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Development of an isotope dilution laser ablation ICP-MS method for multi-element determination in crude and fuel oil samples

2009

An inductively coupled plasma isotope dilution mass spectrometric (ICP-IDMS) method with direct introduction of the isotope-diluted sample into the plasma by laser ablation was developed for accurate, sensitive, fast, and simultaneous determination of trace metals in different oil samples. Metallo-organic solutions of isotope spikes (50V, 53Cr, 65Cu, 57Fe, 62Ni, 68Zn, 113Cd, 117Sn, and 206Pb) were prepared from corresponding aqueous stock solutions by using liquid–liquid extraction of complexed metal ions in isobutyl methyl ketone. The isotope-diluted sample was absorbed by a cellulose material, which was fixed in a special PTFE holder for ablation, using a laser system with high ablation r…

Detection limitLaser ablationChromatographyChemistryAnalytical chemistryVanadiumchemistry.chemical_elementFuel oilFractionationIsotope dilutionAnalytical ChemistryInductively coupled plasmaInductively coupled plasma mass spectrometrySpectroscopyJournal of Analytical Atomic Spectrometry
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A study on the adsorption voltammetry of titanium with various heterocyclic azo-compounds

1994

The voltammetric behaviour of various heterocyclic azo-compounds and their Ti-complexes was investigated at a stationary Hg electrode. In moderately acidic solutions Ti(IV) reacts with pyridylazo-compounds (PAR, 5-Br-PADAP, PAN), thiazolylazo-compounds (TAR, 5-Me-TAR, TAN, 4-Me-TAP) and pyrazolylazo-compounds (MDR, ERB) to form Ti-complexes, which are strongly adsorbed onto the Hg-electrode. These complexes are reduced at potentials more negative than those corresponding to the reduction of their respective ligands. The conditions for determining titanium by adsorption voltammetry using TAR and MDR as complexing agents were investigated in detail, as was the influence of foreign ions on the…

Detection limitMERCUREAzo compoundTrace AmountsChemistryInorganic chemistrychemistry.chemical_elementBiochemistryAnalytical Chemistrychemistry.chemical_compoundAdsorptionElectrodeVoltammetryTitaniumFresenius' Journal of Analytical Chemistry
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