Search results for "Trace Amounts"

showing 10 items of 16 documents

Colorimetric quantitation of trace amounts of sodium lauryl sulfate in the presence of nucleic acids and proteins

1992

A fast and sensitive procedure for the colorimetric detection of sodium lauryl sulfate (SDS) is presented. The assay is based upon the formation of a chloroform-extractable ion pair between lauryl sulfate and methylene blue that is quantified spectrophotometrically with an estimated detection limit of 150 ng of SDS. The method is suitable for the monitoring of contaminating traces of SDS in protein or nucleic acid samples that have the potential to interfere with enzymatic manipulations such as proteolytic digest, restriction analysis, or reverse transcription. Since the procedure is extremely simple and no special equipment is required it is accessible to every researcher concerned with SD…

1303 BiochemistryTrace AmountsSodiumBiophysicschemistry.chemical_element10050 Institute of Pharmacology and Toxicology610 Medicine & healthBiochemistry1307 Cell Biologychemistry.chemical_compoundNucleic Acids1312 Molecular BiologyAnimalsSulfateColorimetryMolecular BiologyDetection limitChromatographyProteinsSodium Dodecyl SulfateCell BiologyDNAReference StandardsRatsMethylene BluechemistryNucleic acidRNA570 Life sciences; biologyCattleColorimetryQuantitative analysis (chemistry)Methylene blue1304 Biophysics
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Inkjet printing Ag nanoparticles for SERS hot spots

2018

A novel inkjet printing based approach is developed for the fabrication of a customizable platform on glass substrates allowing for surface enhanced Raman spectroscopy (SERS) detection of analytes up to single hot spots generated by the spontaneous aggregation of Ag nanoparticles (Ag NPs) in pL scale droplets. After drying the printed droplets under ambient conditions, trace amounts of the analyte can be detected by SERS given the proximity to NP hot spots. By employing alizarin (10-5M) as a model system and scaling the ink droplet volume from 1 nL to 10 pL, the absolute quantity of hot spots has been derived in the printed droplets allowing detecting up to a few molecules in proximity to i…

AnalyteMaterials scienceFabricationTrace AmountsGeneral Chemical EngineeringAnalytical chemistrysers raman spectroscopy nanoparticles02 engineering and technology010402 general chemistryAlizarin01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundColloidraman spectroscopyEngineering (all)MoleculeChemical Engineering (all)sersInkwellGeneral EngineeringSurface-enhanced Raman spectroscopy021001 nanoscience & nanotechnology0104 chemical scienceschemistrynanoparticles0210 nano-technology
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Identification and quantitation of trace amounts of barbiturates with glass capillary gas chromatography

1979

Pre-chromatographic reactions are no longer a necessary evil. Equipment such as the microrefluxer now allows reproducible 7-μl-reactions to be carried out in a short time. Thus multiple derivatisations can be used together with glass capillary GC for routine identifications. The method has been succesfully applied to barbiturates. Retention data of their methyl-, allyl- and benzyl-derivatives are given. Quantitative blood level determinations are briefly discussed.

Blood levelChromatographyTrace AmountsChemistryCapillary actionGeneral Chemical EngineeringGas chromatographyCapillary gas chromatographyJournal of High Resolution Chromatography
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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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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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Trace determination of volatile polycyclic aromatic hydrocarbons in natural waters by magnetic ionic liquid-based stir bar dispersive liquid microext…

2017

In this work, a novel hybrid approach called stir bar dispersive liquid microextraction (SBDLME) that combines the advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) has been employed for the accurate and sensitive determination of ten polycyclic aromatic hydrocarbons (PAHs) in natural water samples. The extraction is carried out using a neodymium stir bar magnetically coated with a magnetic ionic liquid (MIL) as extraction device, in such a way that the MIL is dispersed into the solution at high stirring rates. Once the stirring is ceased, the MIL is magnetically retrieved onto the stir bar, and subsequently subjected to thermal desorptio…

Detection limitMagnetic ionic liquidChromatographyTrace AmountsChemistry010401 analytical chemistryExtraction (chemistry)Analytical chemistryThermal desorption02 engineering and technology021001 nanoscience & nanotechnologyMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistryTap waterIonic strength0210 nano-technologyTalanta
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Determination of ultraviolet filters in bathing waters by stir bar sorptive–dispersive microextraction coupled to thermal desorption–gas chromatograp…

2015

In this work, a new approach that combines the advantages of stir bar sorptive extraction (SBSE) and dispersive solid phase extraction (DSPE), i.e. stir bar sorptive-dispersive microextraction (SBSDµE), is employed as enrichment and clean-up technique for the sensitive determination of eight lipophilic UV filters in water samples. The extraction is accomplished using a neodymium stir bar magnetically coated with oleic acid-coated cobalt ferrite magnetic nanoparticles (MNPs) as sorbent material, which are detached and dispersed into the solution at high stirring rate. When stirring is stopped, MNPs are magnetically retrieved onto the stir bar, which is subjected to thermal desorption (TD) to…

Detection limitSorbentChromatographyTrace AmountsChemistry010401 analytical chemistryExtraction (chemistry)Analytical chemistryThermal desorption02 engineering and technology021001 nanoscience & nanotechnologyMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistrySolid phase extractionGas chromatography–mass spectrometry0210 nano-technologyTalanta
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Atomic fluorescence spectrometric determination of trace amounts of arsenic and antimony in drinking water by continuous hydride generation

1999

A highly sensitive and simple method has been developed for the determination of As(III), total As, Sb(III) and total Sb in drinking water samples by continuous hydride generation and atomic fluorescence spectrometry (HGAFS). For As determination, water samples aspirated in a carrier of 2 mol l(-1) HCl were merged with a reducing NaBH(4) 3%(m/v) solution, with sample and NaBH(4) flow rates of 12.5 and 1.5 ml min(-1) respectively. The hydride generated in a 170 cm reaction coil was transported to the detector with an Ar flow of 400 ml min(-1), and a limit of detection between 5 and 20 ng l(-1) was obtained. For Sb determination, 2.5 mol l(-1) HCl and 2%(m/v) NaBH(4) were employed, with respe…

Detection limitchemistryAntimonyTrace AmountsHydrideAnalytical chemistrychemistry.chemical_elementIodineAtomic fluorescence spectrometryArsenicAnalytical ChemistryVolumetric flow rateTalanta
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Domain Structures in Langmuir-Blodgett Films Investigated by Atomic Force Microscopy

1993

Investigations of phase-separated Langmuir-Blodgett films by atomic force microscopy reveal that on a scale of 30 to 200 micrometers, these images resemble those observed by fluorescence microscopy. Fine structures (less than 1 micrometer) within the stearic acid domains were observed, which cannot be seen by conventional optical microscopic techniques. By applying the force modulation technique, it was found that the elastic properties of the domains in the liquid condensed phase and grains observed within the liquid expanded phase were comparable. Small soft residues in the domains could also be detected. The influence of trace amounts of a fluorescence dye on the micromorphology of monol…

Micrometrechemistry.chemical_compoundMultidisciplinarychemistryTrace AmountsPhase (matter)MonolayerAnalytical chemistryFluorescence microscopeStearic acidFluorescenceLangmuir–Blodgett filmScience
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Trace element analysis in pre-solar stardust grains via full-field imaging XPS (Nano-ESCA)

2006

An acid-resistant, SiC-rich, residue from the Murchison meteorite was investigated by means of a novel imaging XPS instrument. The micrometer-sized grains were deposited on a Si wafer from an aqueous suspension. Energy filtered ESCA images have been taken in the kinetic energy range from the threshold up to about 400 eV for various photon energies. A lateral resolution of the order of 120 nm along with a high energy resolution in the range of 100 meV provides the basis for chemical trace element analysis with maximum sensitivity. Apart from major (Si, C) and minor (N, Mg, Al, Fe) elements, the energy filtered images and local microspectra revealed the presence of a variety of heavy trace el…

Murchison meteoriteNuclear and High Energy PhysicsMaterials scienceTrace AmountsX-ray photoelectron spectroscopyAnalytical chemistryNatural abundanceSpectroscopyKinetic energyInstrumentationMicroanalysisElectron spectroscopyNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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