Search results for "Detection limit"

showing 10 items of 810 documents

The natural compound chrysosplenol-D is a novel, ultrasensitive optical sensor for detection of Cu(II)

2020

Abstract Herein, we introduce a novel, ultrasensitive optical sensor for determination of Cu(II) ions over the concentration range of 0 to 1 μM Cu(II). The optical sensor is based on the natural molecule chrysosplenol-D (Chp-D) extracted from the flowering plant Chiliadenus montanus (Vahl.) Brullo. Free Chp-D emits fluorescence at 566 nm when excited at 292 nm. Chp-D chelates Cu(II) ions to form a 1:1 (metal:ligand) complex, which quenches the fluorescence emission peak of the free probe at 566 nm. “Turn-off” luminescence could be easily determined and provided distinct proof of the chelation of Cu(II) ions by Chp-D. This novel optical sensor offers a considerable fluorescence mechanism (ch…

Detection limitChemistryAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsCharge-transfer complex01 natural sciencesFluorescenceBinding constantAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialssymbols.namesakeLinear rangeStokes shiftMaterials ChemistrysymbolsMoleculePhysical and Theoretical Chemistry0210 nano-technologyLuminescenceSpectroscopyJournal of Molecular Liquids
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A portable and low cost equipment for flow injection chemiluminescence measurements.

2004

A compact, reliable and low cost flow injection chemiluminescence system is described. The flow system consists of a set of solenoid micro-pumps that can dispense reproductive micro-volumes of solutions. The luminometer was based on a coiled cell constructed from polyethylene tubing that was sandwiched between two large area photodiodes. The whole equipment costs about US$ 750 and weights ca. 3 kg. Equipment performance was evaluated by measuring low concentrations of hydrogen peroxide by oxidation of luminol and for the determination of ammonium, based on its inhibition of the luminescence provided by the reaction of luminol and sodium hypochlorite. Linear responses were achieved within 1.…

Detection limitChemistryAnalytical chemistryHypochloriteAnalytical ChemistryLuminollaw.inventionchemistry.chemical_compoundlawReagentSodium hypochloriteHydrogen peroxideLuminescenceChemiluminescenceTalanta
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Improvement of the detection limit for determination of 129I in sediments by quadrupole inductively coupled plasma mass spectrometer with collision c…

2004

The previously developed sample introduction device for the hot extraction of iodine from environmental samples (soils or sediments) and on-line introduction of analyte via the gas phase in quadrupole inductively coupled plasma mass spectrometry with hexapole collision cell (ICP-CC-QMS) was equipped with a cooling finger, which allowed intermediate iodine enrichment and improved the detection limits for I-129 down to 0.4 pg g(-1) without any additional sample preparation. A mixture of oxygen and helium as reaction gases in the hexapole collision cell was used for reducing the disturbing background intensity of Xe-129(+). Oxygen was also used as the carrier gas for iodine thermal desorption …

Detection limitChemistryAnalytical chemistryThermal desorptionchemistry.chemical_elementMass spectrometryJAnalytical Chemistryddc:540QuadrupoleSample preparationInductively coupled plasmaInductively coupled plasma mass spectrometrySpectroscopyHeliumJournal of Analytical Atomic Spectrometry
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Determination of chromium(III) and chromium(VI) in mineral water by bidirectional electrostacking and electrothermal atomic absorption spectrometry

2001

Abstract A feasibility investigation was carried out on the use of bidirectional electrostacking for simultaneous separation and pre-concentration of Cr(III) and Cr(VI) and their electrothermal atomic absorption spectrometry (ETAAS) determination. The bidirectional electrostacking manifold was improved, and the effects of sample tube cross-section and electrostacking time on the pre-concentration factor were investigated. Results indicate that the sample tube cross-section and electrostacking time are the main influence factors on the electrostacking pre-concentration, as well as the electric field strength and ionic mobility. The method developed was suitable for the simultaneous separatio…

Detection limitChemistryAnalytical chemistrychemistry.chemical_elementConductivityBiochemistryAnalytical Chemistrylaw.inventionChromiumCertified reference materialslawStandard additionCalibrationEnvironmental ChemistryAtomic absorption spectroscopyQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Cr(III)/Cr(VI) speciation in aerosol particles by extractive separation and thermal ionization isotope dilution mass spectrometry

1997

An isotope dilution mass spectrometric (IDMS) method, using the formation of positive thermal ions, was developed for Cr(III) and Cr(VI) speciation in aerosol particles. Cr(III) and Cr(VI) spike species, enriched in 53Cr, were applied for the isotope dilution step. After leaching of filter collected aerosol samples by an alkaline solution at pH 13, species separation was carried out by extraction with a liquid anion exchanger in methyl isobutyl ketone. Cr(VI) in the organic phase was re-extracted into an ammoniacal solution and chromium was then isolated from both fractions of species by electrodeposition. Detection limits of 30 pg/m3 for Cr(III) and of 8 pg/m3 for Cr(VI) were achieved in a…

Detection limitChemistryAnalytical chemistrychemistry.chemical_elementIsotope dilutionMass spectrometryBiochemistryAerosolMethyl isobutyl ketonechemistry.chemical_compoundChromiummedia_common.cataloged_instanceLeaching (metallurgy)European unionmedia_commonFresenius' Journal of Analytical Chemistry
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Multicommutation Fourier transform infrared determination of benzene in gasoline

2004

A fully mechanized method to determine benzene in motor gasolines has been developed based on the use of Fourier transform infrared spectroscopy (FT-IR) and multicommutation. The flow network comprised a set of three-way solenoid valves and was controlled by means of a microcomputer furnished with an electronic interface and running by a software written in QUICK BASIC 4.5. The flow network and control software were designed to implement the multicommutation approach providing facilities to handle sample and reagent solutions, so that, sample dilution, external calibration and standard addition could be easily performed on-line. The method permits the direct determination of benzene without…

Detection limitChemistryDirect methodAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformStandard additionsymbolsEnvironmental ChemistryGasolineFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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2,4,6-Triphenylpyrylium Ion Encapsulated into Zeolite Y as a Selective Electrode for the Electrochemical Determination of Dopamine in the Presence of…

2002

2,4,6-Triphenylpyrylium ion immobilized inside the supercages of zeolite Y enhances by 1-2 orders of magnitude the response of electrochemical oxidation of dopamine in neutral aqueous media accompanied by a remarkable inhibition of post-electron-transfer reactions. The negative charge of the zeolite framework in which the 2,4,6-triphenylpyrylium ion is incorporated blocks the electrochemical oxidation of the negative ascorbate ion, enabling the determination of micromolar concentrations of dopamine in the presence of a large excess (10(3)-10(4) times) of ascorbate in phosphate buffer (pH 7.4). Under optimized conditions, linear calibration plots were obtained for a differential pulse detect…

Detection limitChemistryDopamineInorganic chemistryAscorbic AcidElectrochemistryAscorbic acidSensitivity and SpecificityOrders of magnitude (mass)Analytical ChemistryIonDopamineCalibrationElectrodeElectrochemistryZeolitesmedicineZeoliteElectrodesOxidation-ReductionPyransmedicine.drugAnalytical Chemistry
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dsDNA, ssDNA, G-quadruplex DNA, and nucleosomal DNA electrochemical screening using canthin-6-one alkaloid-modified electrodes

2014

Abstract Microparticulate films of a canthin-6-one alkaloid ( L ), a natural β-carboline alkaloid presenting a characteristic naphtyridone motif, on glassy carbon electrodes yield different, separate voltammetric signals for dsDNA, ssDNA, G-quadruplex DNA, different degrees of DNA methylation and the biomimetic nucleosomal DNA with detection limit of 10 −5  M. This multiple-signal electrochemical behavior is in contrast with conventional use of DNA intercalators, only discriminating between different DNA forms by variations in the intensity of a unique signal. Complementary photochemical and scanning electrochemical microscopy (SECM) data suggest that the differences in the voltammetric res…

Detection limitChemistryGeneral Chemical EngineeringIntercalation (chemistry)Glassy carbonG-quadruplexElectrochemistrychemistry.chemical_compoundScanning electrochemical microscopyBiochemistryDNA methylationElectrochemistryBiophysicsDNAElectrochimica Acta
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Determination of Concentration Profiles of Methyl Mercury Compounds in Surface Waters of Polar and other Remote Oceans by GC-AFD

1998

Abstract The concentration of monomethyl mercury (MeHg+) and dimethyl mercury (Me2Hg) was determined in surface sea-water samples of the Antarctic and Arctic Ocean as well as of other remote areas (South Atlantic and South Pacific) during expeditions of the German research vessel “Polarstern”. A purge and trap/gas chromatographic system, equipped with an atomic fluorescence detector (AFD), was used. For the analysis of MeHg+ conversion into the volatile methylethyl mercury by reaction with tetraethyloborate prior to the purging process was carried out. The detection limit for both methylated mercury compounds was 5 pg Hg/L, which allowed their determination in most ocean water samples even …

Detection limitChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthSoil Sciencechemistry.chemical_elementPollutionFluorescence spectroscopyAnalytical ChemistryMercury (element)ArcticEnvironmental chemistryEnvironmental ChemistryPolarSeawaterGas chromatographyWater pollutionWaste Management and Disposalgeographic locationsWater Science and TechnologyInternational Journal of Environmental Analytical Chemistry
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Atomic absorption spectrometric determination of molybdenum in lubricating oils with use of emulsions

1985

Abstract Samples (0.1 g) containing molybdenum disulphide are digested with aqua regia or with a (1 + 1) hydrofluoric/nitric acid mixture, without complete destruction of the matrix, and the molybdenum is determined in an air/acetylene flame, after emulsification with a non-ionic surfactant (Nemol K-39). The detection limit is ca. 30 μg Mo g−1, and the r.s.d. is 2.9% for 6 analyses of a sample containing 6.5 mg Mo g−1.

Detection limitChemistryInorganic chemistrychemistry.chemical_elementBiochemistryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundAcetylenePulmonary surfactantNitric acidMolybdenumlawEnvironmental ChemistryAqua regiaAtomic absorption spectroscopySpectroscopyAnalytica Chimica Acta
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