Search results for "solution"

showing 10 items of 5638 documents

Sun-induced fluorescence - a new probe of photosynthesis: First maps from the imaging spectrometer HyPlant.

2015

Variations in photosynthesis still cause substantial uncertainties in predicting photosynthetic CO2 uptake rates and monitoring plant stress. Changes in actual photosynthesis that are not related to greenness of vegetation are difficult to measure by reflectance based optical remote sensing techniques. Several activities are underway to evaluate the sun-induced fluorescence signal on the ground and on a coarse spatial scale using space-borne imaging spectrometers. Intermediate-scale observations using airborne-based imaging spectroscopy, which are critical to bridge the existing gap between small-scale field studies and global observations, are still insufficient. Here we present the first …

Chlorophyllinduced fluorescencesunImaging spectrometer2306 Global and Planetary ChangeFluorescence2300 General Environmental SciencePhotosynthesiEnvironmental ChemistryAirborne measurement910 Geography & travelSpectral resolutionPhotosynthesisAbsorption (electromagnetic radiation)Spectroscopyairborne measurementsChlorophyll fluorescenceGeneral Environmental ScienceRemote sensingGlobal and Planetary ChangeSpectrometerEcology2300Remote sensingImaging spectroscopyVegetation monitoringFLEXImaging spectroscopy10122 Institute of GeographyGEO/10 - GEOFISICA DELLA TERRA SOLIDASpectrometry FluorescenceSun-induced fluorescence2304 Environmental ChemistryHyPlantRemote Sensing TechnologySunlightEnvironmental scienceSpatial variabilityChlorophyll fluorescence2303 EcologyGlobal change biology
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Cr(VI) sorption by intact and dehydrated Candida utilis cells in the presence of other metals

2002

This study examined the Cr(VI), Cu(II), Zn(II), Cd(II), Pb(II) sorption by intact and dehydrated Candida utilis cells. The anion [Cr2O7]2− and cation Me2+ sorption kinetics was investigated in both single- and dual-metal situations. Uptake of chromate anions occurred much more slowly singularly than with metal cations. A combination of Pb or Cu and chromate anions gave a synergistic effect for Cr(VI) sorption, but not Cd and Zn, which inhibited Cr(VI) sorption by dehydrated cells. The use of alcian blue to occupy maximum vacant adsorption sites on the cell surface unexpectedly did not influence further adsorption of Me2+. Metal uptake by C. utilis was 7 mg (135 μM) Cr, 23 mg (362 μM) Cu, 39…

Chromate conversion coatingChemistryMetal ions in aqueous solutionInorganic chemistrySorption kineticsBioengineeringHeavy metalsSorptionApplied Microbiology and BiotechnologyBiochemistryIonMetalAdsorptionvisual_artvisual_art.visual_art_mediumProcess Biochemistry
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Behavior of Flavor Compounds in Model Food Systems:  a Thermodynamic Study

2003

Physicochemical parameters, such as hydrophobicity, water solubility, and volatility, of four flavor compounds (ethyl acetate, ethyl butyrate, ethyl hexanoate, and 2-pentanone) were determined. The amount of flavor compounds released from different model matrices (mineral water, purified triolein, an oil-in-water emulsion, a carbohydrate matrix, and a complex matrix containing lipids and carbohydrates) into the gaseous phase was determined at thermodynamic equilibrium, at 37 degrees C, by static headspace gas chromatography. The degree of interaction between the flavor compounds and the matrix components was shown by measuring the percentage retention using the water matrix as the reference…

Chromatography GasCarbohydratesEthyl acetateAcetateschemistry.chemical_compoundEthyl butyratePentanonesOrganic chemistryTrioleinCaproatesFlavorAqueous solutionChromatographyViscosityfood and beveragesEthyl hexanoateGeneral Chemistryequipment and suppliesButyratesSolubilitychemistryTasteOdorantsEmulsionThermodynamicsGas chromatographyVolatilizationRheologyGeneral Agricultural and Biological SciencesFood AnalysisJournal of Agricultural and Food Chemistry
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A Method to Quantitatively Trap Volatilized Organoselenides for Stable Selenium Isotope Analysis

2011

If volatile organoselenides are to be analyzed for their stable Se isotope composition to elucidate sources and formation processes, organoselenides need to be trapped quantitatively to avoid artificial Se isotope fractionation. We developed an efficient trap of organoselenides to be used in microcosms designed to determine the Se isotope fractionation by microbial transformation of inorganic Se to volatile organoselenides. The recoveries of volatilized dimethyldiselenide (DMDSe) from aqueous standard solutions by activated charcoal and alkaline peroxide solution with subsequent freeze-drying and purification via a cation exchange resin were tested. Microcosm experiments with the Se-methyla…

Chromatography GasEnvironmental EngineeringAqueous solutionIsotopeChemistryRadiochemistryAlternariaManagement Monitoring Policy and LawPollutionPeroxidesSeleniumIsotopes of seleniumIsotope fractionationIsotopesActivated charcoalCharcoalOrganoselenium CompoundsComposition (visual arts)VolatilizationMicrocosmIon-exchange resinWaste Management and DisposalEnvironmental MonitoringWater Science and TechnologyJournal of Environmental Quality
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Biogenic synthesis of palladium nanoparticles using Pulicaria glutinosa extract and their catalytic activity towards the Suzuki coupling reaction.

2014

Green synthesis of nanomaterials finds the edge over chemical methods due to its environmental compatibility. Herein, we report a facile and eco-friendly method for the synthesis of palladium (Pd) nanoparticles (NPs) using an aqueous solution of Pulicaria glutinosa, a plant widely found in a large region of Saudi Arabia, as a bioreductant. The as-prepared Pd NPs were characterized using ultraviolet-visible (UV-vis) spectroscopy, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform-infrared spectroscopy (FT-IR). The hydroxyl groups of the plant extract (PE) molecules were found mainly responsible for the red…

Chromatography GasMagnetic Resonance SpectroscopyStereochemistrychemistry.chemical_elementNanoparticleLigandsCatalysisCatalysisNanomaterialsPulicariaInorganic ChemistrySuzuki reactionMicroscopy Electron TransmissionX-Ray DiffractionSpectroscopy Fourier Transform InfraredMoleculeAqueous solutionChemistryPlant ExtractsX-RaysTemperatureGreen Chemistry TechnologyTransmission electron microscopyNanoparticlesSpectrophotometry UltravioletPalladiumNuclear chemistryPalladiumBromobenzenesDalton transactions (Cambridge, England : 2003)
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Determination of 2,3,7,8-tetrachlorodibenzo-p-dioxin in goat milk and tissues by glass capillary gas chromatography and medium resolution mass fragme…

1981

Abstract An analytical method has been developed for the study of the elimination of 2,3,7,8-tetrachlodoribenzo-p-dioxin (TCDD) by lactation and its determination in various tissues of goat. The method is based on the alkaline hydrolysis of milk, liver, fat, muscle, blood, faeces and urine samples, extraction with n-hexane, treatment with sulphuric acid-saturated silica gel, chromatographic clean-up on silica gel and alumina micro-columns, and glass capillary gas chromatography—medium resolution mass fragmenography (resolution 2000). 1,2,3,4-Tetrachlorodibenzo-p-dioxin is used as the internal standard, the concentration of TCDD being determined from the calibration curve calculated from the…

Chromatography GasPolychlorinated DibenzodioxinsResolution (mass spectrometry)Calibration curveUrine010501 environmental sciencesDioxins01 natural sciencesBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundLactationmedicineAnimalsTissue Distributionheterocyclic compounds0105 earth and related environmental sciencesDetection limitReproducibilityChromatographySilica gelGoatsMuscles010401 analytical chemistryOrganic ChemistryExtraction (chemistry)General Medicine0104 chemical sciencesMilkmedicine.anatomical_structureLiverchemistryJournal of Chromatography A
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Pullulan and dextran: uncommon composition dependent Flory-Huggins interaction parameters of their aqueous solutions.

2008

Vapor pressure measurements were performed for aqueous solutions of pullulan ( M w 280 kg/mol) and dextran ( M w 60 and 2100 kg/mol, respectively) at 25, 37.5, and 50 degrees C. The Flory-Huggins interaction parameters obtained from these measurements, plus information on dilute solutions taken from the literature, show that water is a better solvent for pullulan than for dextran. Furthermore, they evince uncommon composition dependencies, including the concurrent appearance of two extrema, a minimum at moderate polymer concentration and a maximum at high polymer concentration. To model these findings, a previously established approach, subdividing the mixing process into two clearly separa…

Chromatography GasPolymers and PlasticsVapor pressureThermodynamicsBioengineeringFlory–Huggins solution theoryBiomaterialschemistry.chemical_compoundMaterials ChemistryPressureSolubilityGlucanschemistry.chemical_classificationAqueous solutionChromatographyWaterPullulanDextransPolymerSolventMolecular WeightDextranchemistryModels ChemicalSolventsThermodynamicsBiomacromolecules
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Comparison of surfactant-mediated liquid chromatographic modes with sodium dodecyl sulphate for the analysis of basic drugs

2020

In reversed-phase liquid chromatography (RPLC), basic drugs are positively charged at the usual working pH range and interact with free anionic silanols present in conventional silica-based stationary phases. This translates into stronger retention and tailed and broadened peaks. This problem can be resolved by the addition of reagents to the mobile phase that are adsorbed on the stationary phase, avoiding the access of solutes to silanols. Among these additives, surfactants under micellar conditions have provided good silanol suppressing potency through the technique known as micellar liquid chromatography (MLC). The most common example of this is anionic sodium dodecyl sulphate (SDS). Whe…

Chromatography Reverse-PhaseAqueous solutionChromatographyChemistryGeneral Chemical Engineering010401 analytical chemistryGeneral EngineeringSodium Dodecyl Sulfate02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMicelle0104 chemical sciencesAnalytical ChemistrySurface-Active AgentsSilanolchemistry.chemical_compoundPulmonary surfactantMicellar liquid chromatographyReagentPhase (matter)Microemulsion0210 nano-technologyMicellesChromatography LiquidAnalytical Methods
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Approaches to characterise chromatographic column performance based on global parameters accounting for peak broadening and skewness.

2009

Peak broadening and skewness are fundamental parameters in chromatography, since they affect the resolution capability of a chromatographic column. A common practice to characterise chromatographic columns is to estimate the efficiency and asymmetry factor for the peaks of one or more solutes eluted at selected experimental conditions. This has the drawback that the extra-column contributions to the peak variance and skewness make the peak shape parameters depend on the retention time. We propose and discuss here the use of several approaches that allow the estimation of global parameters (non-dependent on the retention time) to describe the column performance. The global parameters arise f…

Chromatography Reverse-PhaseChromatographyAcetonitrilesResolution (mass spectrometry)ChemistryElutionOrganic ChemistryAdrenergic beta-AntagonistsLinear modelNormal DistributionGeneral MedicineReversed-phase chromatographyBiochemistryColumn (database)Standard deviationAnalytical ChemistryNormal distributionModels ChemicalSkewnessBenzene DerivativesLinear ModelsDiureticsJournal of chromatography. A
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Finding the best separation in situations of extremely low chromatographic resolution.

2010

Abstract Samples with a large number of compounds or similarities in their structure and polarity may yield insufficient chromatographic resolution. In such cases, however, finding conditions where the largest number of compounds appears sufficiently resolved can be still worthwhile. A strategy is here reported that optimises the resolution level of chromatograms in cases where conventional global criteria, such as the worst resolved peak pair or the product of elementary resolutions, are not able to detect any separation, even when most peaks are baseline resolved. The strategy applies a function based on the number of “well resolved” peaks, which are those that exceed a given threshold of…

Chromatography Reverse-PhaseChromatographyAcetonitrilesResolution (mass spectrometry)ChemistryLow resolutionOrganic ChemistrySeparation (aeronautics)Analytical chemistryGeneral MedicineFunction (mathematics)Partial resolutionHydrogen-Ion ConcentrationBiochemistryAnalytical ChemistryChromatographic separationModels ChemicalYield (chemistry)Organic ChemicalsJournal of chromatography. A
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