Search results for "Spectroscopy"

showing 10 items of 10293 documents

Catalytic CO oxidation over pumice supported Pd–Ag catalysts

2001

Abstract Results on the catalytic oxidation of CO at 523 K over bimetallic Pd–Ag catalysts supported on pumice are reported and compared with those obtained from the monometallic Pd and Ag catalysts. The catalysts were prepared by organometallic precursors and were characterized by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) after different treatments with air and with hydrogen. The activity of the catalysts decreases with increasing Ag/Pd atomic ratio, the monometallic palladium exhibiting the highest activity. Furthermore, the treatment with air and with hydrogen always results in a better catalytic performance. On the basis of the structural characterization by XRD…

Transition metalHydrogenX-ray photoelectron spectroscopyCatalytic oxidationChemistryProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementAtomic ratioBimetallic stripCatalysisPalladiumCatalysisApplied Catalysis A: General
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A penning trap for studying cluster ions

2008

We propose to use a Penning trap for spectroscopy of stored cluster ions. A similar device has been built for the purpose of mass measurements of short-lived nuclei produced at the on-line isotope separator ISOLDE/CERN. A resolving power of 500,000 in a mass measurement of39K and an accuracy of 2 × 10−7 for the85Rb/39K mass ratio were obtained. An efficiency for in-flight capture as high as 70% was achieved. The method provides very high sensitivity since typically only 10 to 100 ions are stored in the trap. We intend to perform laser spectroscopy on trapped Na clusters as a first application of the trap technique.

Trap (computing)Materials scienceIsotopeCluster (physics)Separator (oil production)Physics::Atomic PhysicsAtomic physicsMass ratioSpectroscopyPenning trapIon
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Experimental studies at JYFLTRAP

2007

JYFLTRAP is a Penning trap system at the accelerator laboratory in Jyvaskyla, Finland that enables high-precision experiments with stored, exotic species that are produced at the IGISOL facility. On one hand, these can be performed within the trap itself, like e.g. mass spectrometry. On the other hand, the trap can be used to provide the highly purified species for further experiments, e.g. for trap-assisted nuclear decay spectroscopy. This contribution focuses on these two possible applications with the presentation of some recent results on superallowed beta decays.

Trap (computing)Nuclear physicsChemistryQ valueMass spectrometryPenning trapSpectroscopyAtomic massRadioactive decay
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Conversion of nadir, narrowband reflectance in red and near-infrared channels to hemispherical surface albedo

1997

Abstract Measured nadir-viewed narrow-band reflectanees in red and near infrared channels simulating AVHRR Channels 1 and 2 are compared with measured integrated solar spectrum hemispherical albedos. Reflectanees and albedos were measured from an aircraft over four widely different vegetation surfaces in southeastern Tasmania (Australia). A linear function is used to simultaneously correct for narrow band to broad band conversion errors and to convert nadir viewed reflectances to hemispherical albedos. While the application of the conversion equation presented is limited to the vegetation types of the study, the equation is independent of vegetation type. Results indicate that the reflectan…

Tree canopybusiness.industryNear-infrared spectroscopySoil ScienceBeer–Lambert lawGeologyVegetationAlbedoMultispectral Scannersymbols.namesakeNarrowbandOpticssymbolsNadirEnvironmental scienceComputers in Earth SciencesbusinessRemote sensingRemote Sensing of Environment
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Lipid phase transition in saccharide-coated cholate-containing liposomes: coupling to the surrounding matrix.

2005

We performed FTIR measurements on cholate-containing liposomes (CCL) embedded in saccharide (trehalose or sucrose) matrixes with different contents of residual water. We obtained information on the CCL phase transition following the thermal evolution (310-70 K) of the IR spectrum of the carbonyl moieties of phospholipids in the frequency range 4225-4550 cm(-1). Furthermore, we simultaneously followed the thermal evolution of the water association band, which gave information on the behavior of the surrounding water-saccharide matrix. The analysis revealed a small sub-band of the water association band present in CCL but not in cholate-free liposomes, the thermal evolution of which is tightl…

Trehalose Liposomes Thermal behaviourSucroseSucroseSurface PropertiesLipid BilayersPhospholipidInfrared spectroscopydigestive systemPermeabilityPhase Transitionchemistry.chemical_compoundDrug Delivery Systemsstomatognathic systemHydrophilySpectroscopy Fourier Transform InfraredElectrochemistryGeneral Materials ScienceLipid bilayer phase behaviorFourier transform infrared spectroscopySpectroscopyPhospholipidsLiposomeChromatographydigestive oral and skin physiologyTemperatureTrehaloseWaterSurfaces and InterfacesCondensed Matter PhysicsTrehaloseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)chemistryLiposomesCholatesHydrophobic and Hydrophilic InteractionsLangmuir : the ACS journal of surfaces and colloids
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Analysis of Diuretics in Urine by Column-Switching Chromatography and Fluorescence Detection

1997

The potential of column-switching chromatography and fluorescence detection for the analysis of diuretics in urine is evaluated. Sample cleanup and chromatographic parameters have been optimized to achieve maximum sensitivity for the detection and quantification of some relevant diuretics. On the basis of these studies, an on-line procedure for the simultaneous determination of amiloride, furosemide, bumetanide and triamterene is presented. The linearity, precision, accuracy and sensitivity of the method are discussed. The utility of the described approach has been tested by analysing urine samples obtained after administration of bumetanide.

TriamtereneChromatographyChemistrymedicine.drug_classmedicine.medical_treatmentClinical BiochemistryPharmaceutical ScienceUrineBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical ChemistryPotassium-sparing diureticmedicineDiureticQuantitative analysis (chemistry)Bumetanidemedicine.drugJournal of Liquid Chromatography & Related Technologies
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Chromatographic monitoring of diuretics in urine samples using a sodium dodecyl sulphate—propanol micellar eluent

1994

Abstract The effect of a varying pH, in the range 3−7, on the retention of several diuretics eluted with a sodium dodecyl sulphate (SDS) micellar mobile phase and with UV detection was studied. Significant changes in the capacity factors ( K′ of the diuretics bumetanide, ethacrynic acid, furosemide, probenecid and xipamide were observed. The protonation constants of these compounds were calculated from the k′ data. A study was also performed to select the optimum composition of the mobile phase (pH, concentration of SDS and nature and concentration of alcohol) for the separation of the above diuretics and the diuretics amiloride, bendroflumethiazide, chlorthalidone, hydrochlorothiazide, spi…

TriamtereneChromatographySodiummedicine.medical_treatmentchemistry.chemical_elementBiochemistryAnalytical ChemistryAmilorideHydrochlorothiazidechemistryMicellar solutionsmedicineEnvironmental ChemistryBendroflumethiazideXipamideDiureticSpectroscopymedicine.drugAnalytica Chimica Acta
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Determination of triamterene in urine by HPLC using fluorescence detection and column-switching

1994

A liquid chromatographic method incorporating column-switching and fluorimetric detection for the determination of triamterene in untreated urine, is described. The urine samples (5 μL) were directly introduced onto an Hypersil ODS-C18, 30 μm (20 mm×2.1 mm I.D.) pre-column. Polar urinary compounds were removed by flushing the pre-column with water for 1 min, and the analyte was then switched onto an HP-LiChrospher RP C18,5 μm (125 mm×4mm ID) analytical column using an acetonitrile/phosphate buffer gradient elution. Fluorescence detection was performed at 230 nm excitation and 430 nm emission wavelengths. The recovery of drug was 102±2% in the 0.10–20.0 μg/mL concentration range, the limit o…

TriamtereneDetection limitAnalyteChromatographyChemistryOrganic ChemistryClinical BiochemistryUrineBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundmedicineAcetonitrileQuantitative analysis (chemistry)medicine.drugChromatographia
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Chromatographic determination of diuretics in urine samples using hybrid micellar mobile phases with fluorimetric detection

1998

Abstract A rapid and simple chromatographic procedure, that uses hybrid micellar mobile phases of sodium dodecyl sulphate (SDS), propanol and phosphate buffer at pH 3, and fluorimetric detection ( λ exc =270 nm, λ em =430 nm), is reported for the determination of mixtures of seven diuretics of diverse efficacy (amiloride, bendroflumethiazide, bumetanide, furosemide, hydroflumethiazide, piretanide and triamterene), in urine samples. The application of a sequential optimization procedure for the resolution of the mixtures of the diuretics was problematic. However, their separation was achieved through the use of an interpretive optimization procedure based on the accurate description of the r…

TriamtereneDetection limitHydroflumethiazideChromatographyChemistrymedicine.medical_treatmentPiretanideBiochemistryAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographymedicineEnvironmental ChemistryBendroflumethiazideDiureticSpectroscopyBumetanidemedicine.drugAnalytica Chimica Acta
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Synthesis and Characterisation of Chiral Triazole-Based Halogen-Bond Donors: Halogen Bonds in the Solid State and in Solution

2017

A general platform for the synthesis of various chiral halogen-bond (XB) donors based on the triazole core and the characterisation of factors that influence the strength of the halogen bond in the solid state and in solution are reported. The characterisation of XB donors in the solid state by X-ray crystallography and in solution by 1H NMR titration can be used to aid the design of new XB donors. We describe the first example of a XB between iodotriazoles and thioureas in solution. In addition, the enantiodiscrimination of acceptors in solution through halogen-bond participation is described.

TriazoleSolid-state010402 general chemistry01 natural scienceschemical bondsCatalysiskemialliset sidoksetchemistry.chemical_compoundNMR spectroscopyhalogensOrganic chemistryNMR-spektroskopiata116x-ray crystallographykemiallinen synteesiHalogen bondhalogeenit010405 organic chemistryOrganic ChemistryGeneral ChemistryCombinatorial chemistry0104 chemical scienceschemistryHalogenTitrationröntgenkristallografiachemical synthesisChemistry - A European Journal
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