Search results for "Absorbance"

showing 10 items of 192 documents

Methodical Studies in the Separation of Chlorophyll-Protein Complexes by Polyacrylamide Gel Electrophoresis

1980

Summary Chlorophyll-protein complexes from thylakoids of Sinapis alba plants were separated, using Tris-HCl and Tris-borate buffer in the sodium dodecyl sulphate acrylamide gel electrophoresis. In the electrophoretogram with Tris-borate buffer, 6 bands could be characterized in the gel pattern. In addition to the three major green zones (P-700-chlorophyll a-protein, light-harvesting chlorophyll a/b-protein, free pigment zone), which were also observed in experiments with the Tris-HC1 buffer, three further bands (LHCP 1 , LHCP 2 , CPa) were electrophoretically separated. An elongation of the electrophoretical period resulted especially in a decrease of the proportion of the light-harvesting …

Chlorophyll bChlorophyll aChromatographyElectrophoretogramAnalytical chemistryGeneral MedicineAbsorbanceElectrophoresischemistry.chemical_compoundPigmentchemistryChlorophyllvisual_artvisual_art.visual_art_mediumPolyacrylamide gel electrophoresisZeitschrift für Pflanzenphysiologie
researchProduct

Gaussian processes retrieval of leaf parameters from a multi-species reflectance, absorbance and fluorescence dataset.

2013

Abstract: Biochemical and structural leaf properties such as chlorophyll content (Chl), nitrogen content (N), leaf water content (LWC), and specific leaf area (SLA) have the benefit to be estimated through nondestructive spectral measurements. Current practices, however, mainly focus on a limited amount of wavelength bands while more information could be extracted from other wavelengths in the full range (400-2500 nm) spectrum. In this research, leaf characteristics were estimated from a field-based multi-species dataset, covering a wide range in leaf structures and Chl concentrations. The dataset contains leaves with extremely high Chl concentrations (>100 mu g cm(-2)), which are seldom es…

ChlorophyllSpecific leaf areaNitrogenBiophysicsRed edgeTreesAbsorbancesymbols.namesakeRadiology Nuclear Medicine and imagingGaussian processWater contentBiologyRemote sensingMathematicsRadiationRadiological and Ultrasound TechnologyPhysicsHyperspectral imagingWaterRegression analysisPlant LeavesChemistrySpectrometry FluorescencesymbolsCurve fittingAlgorithmsJournal of photochemistry and photobiology. B, Biology
researchProduct

The intensification of absorbance changes in leaves by light-dispersion

1979

In dispersive samples, like leaves, the absorbance of pigments is intensified. The intensification is due to a longer optical path through the dispersive sample. However, in chloroplast suspensions the optical path is not much longer than in clear solutions. The factor of intensification β (=the lengthening of the optical path) is calculated by comparing the absorbance of leaves and the absorbance of chloroplast suspensions with equal pigment-content. This method also includes the influence of possible sieve effects which could decrease absorbance. The measurements are carried out with high- and low-light leaves of different thickness and pigment content. The intensification of absorbance w…

ChloroplastAbsorbanceCytochrome fPigmentChromatographyChemistryvisual_artLight dispersionGeneticsAnalytical chemistryvisual_art.visual_art_mediumsense organsPlant SciencePlanta
researchProduct

Determination of critical eluent composition for polyethylenglycols using on-line liquid chromatography-Fourier transform infrared spectrometry.

2008

In this work, it has been extended to methanol:water mobile phases, the use of a background correction method for on-line LC-FTIR measurements named Univariate background correction based on the use of a reference spectra matrix (UBC-RSM) and absorbance ratios. It permits to overcome the problem related to spectral changes occurring during the gradient elution, which in the past limited the on-line coupling of LC and FTIR to isocratic elutions. The combined use of the aforementioned background correction technique in on-line isocratic and gradient LC-FTIR, and partial least squares (PLS) has been applied for the search of the critical conditions for polymers. Polyethylenglycol (PEG) has bee…

ChromatographyChemistryAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical ChemistryMatrix (chemical analysis)AbsorbanceColumn chromatographyPartial least squares regressionEnvironmental ChemistryBackground Correction MethodFourier transform infrared spectroscopySpectroscopy
researchProduct

Flow Injection Fourier Transform Infrared Determination of Caffeine in Soft Drinks

1997

A fully automated procedure has been developed for FT-IR determination of caffeine in soft drinks. Samples are first degasified by filtration and then directly injected into a flow manifold and passed through a 100 mg C18 SPE cartridge, conditioned with methanol and water. After the cartridge has been cleaned with water, the caffeine is eluted with CHCl3 and stabilized with ethanol. The flow injection (FI) recording is obtained by measuring the absorbance at 1658 cm-1 with a baseline established at 1800 cm-1. Area values for the FI recording obtained between 0.4 and 1.4 min after sample injection are interpolated in the calibration graph of a series of aqueous standards of caffeine, which w…

ChromatographyChemistryCalibration curveElutionExtraction (chemistry)Analytical chemistryAnalytical Chemistrylaw.inventionAbsorbanceCartridgechemistry.chemical_compoundlawSolid phase extractionCaffeineFiltrationAnalytical Chemistry
researchProduct

Univariate method for background correction in liquid chromatography–Fourier transform infrared spectrometry

2007

An univariate method is proposed for background correction in on-line gradient liquid chromatography-Fourier transform infrared (LC-FTIR) spectrometry using acetonitrile:water as mobile phase components. The method is based on the calculation of the ratio of absorbances (AR) at two characteristic wavenumbers for each spectrum. This parameter is subsequently used to locate the most appropriated eluent spectrum within a reference spectra matrix (RSM) to be subtracted from each spectrum included in the sample chromatogram. To correct minor changes in eluent spectra intensity during the elution of analytes, a correction factor (Kf), defined as the ratio of the absorbance of the sample and the s…

ChromatographyChemistryElutionOrganic ChemistryAnalytical chemistryInfrared spectroscopyGeneral MedicineReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)ChemometricsAbsorbanceDiuronSpectroscopy Fourier Transform InfraredAtrazineFourier transform infrared spectroscopyChromatography LiquidJournal of Chromatography A
researchProduct

Simultaneous determination of acetylsalicylic acid and caffeine in pharmaceuticals by flow injection with fourier transform infrared detection.

1993

Abstract A fast quality control methodology has been developed for the simultaneous determination of acetylsalicylic acid (ASA) and caffeine in pharmaceuticals by flow injection—Fourier Transform Infrared Spectrometry. The method is based on the solubilization of ASA and caffeine in CH2Cl2 and the use of a flow system to introduce samples and standards in the spectrometer. Two solutions, containing 90 and 110% of the reported concentration of the two active principles in the sample, were employed in order to control the extreme tolerance levels accepted by the International Pharmacopeia for the composition of formulations. A 300 μl volume of each solution was injected in turn, into a carrie…

ChromatographyChemistryInfraredInfrared spectroscopyDosage formAnalytical ChemistryAbsorbancesymbols.namesakechemistry.chemical_compoundFourier transformSolubilizationsymbolsCaffeineQuantitative analysis (chemistry)Talanta
researchProduct

The solubilization site of 5,10,15,20-tetrakis-(2,6-dichlorophenyl)-porphyrin-Mn(III) in DPPC vesicles: A spectrophotometric and tensiometric study

2006

Abstract The solubilization site of 5,10,15,20-tetrakis-(2,6-dichlorophenyl)-porphyrin-Mn(III) (MnTDPPC) in l -α-dipalmitoylphosphatidyl choline (DPPC) vesicles was determined in a systematic UV–vis spectrophotometric study. Measurements of the MnTDPPC absorbance have been conducted at constant temperatures (in the interval 30 °C ≤ T ≤ 48 °C) and varying concentrations of phospholipid. In the entire temperature range, the absorption due to MnTDCCP was found to increase with increasing DPPC concentration, until it reaches a plateau value. The data have been analyzed using a pseudo-phase model yielding the binding constant of MnTDCPP to vesicular aggregates. No significant temperature depende…

ChromatographyChemistryVesicletechnology industry and agricultureAqueous two-phase systemAnalytical chemistryPorphyrinBinding constantHydrophobic effectPartition coefficientAbsorbancechemistry.chemical_compoundColloid and Surface ChemistryAbsorption (chemistry)Colloids and Surfaces A: Physicochemical and Engineering Aspects
researchProduct

Filter-based infrared detectors for high temperature size exclusion chromatography analysis of polyolefins: calibration with a small number of standa…

2012

Infrared detection has been shown to be very appropriate for high temperature analysis of polyolefins. After some early reports in which dispersive or single-band filter-based detectors were applied, Fourier transform detectors have been described for this application, in order to improve the method sensitivity. Modern simple filter-based detectors prove, however, comparable sensitivity while providing a number of practical advantages when coupled to chromatographic systems: reduced cell volume, simplified hardware, continuous generation of absorbance chromatograms, as well as simpler data collection and processing. A practical method for calibration, using multiple-band signals obtained wi…

ChromatographyHot TemperatureResolution (mass spectrometry)Spectrophotometry InfraredChemistryOrganic ChemistryDetectorGeneral MedicinePolyenesSignal-To-Noise RatioBiochemistryAnalytical ChemistryAbsorbanceMolecular Weightsymbols.namesakeSignal-to-noise ratioFourier transformFilter (video)CalibrationMultivariate AnalysisCalibrationsymbolsChromatography GelLinear ModelsSensitivity (control systems)Journal of chromatography. A
researchProduct

Kinetic-Spectrophotometric Determination of Primary and Secondary Amines by Reaction with 1-2 Naphthoquinone-4-Sulphonate.

1994

Abstract A kinetic-spectrophotometric method for the determination of primary and secondary amines is described. It is based on the coloured reaction of these amines with sodium 1,2 Naphthoquinone 4-sulphonate (NQS) in the presence of a non-ionic surfactant. For each determination the optimum conditions were studied and found to be as follows: pH 10.5. Carbonate-bicarbonate buffer 0.1M, Triton X-100 0.1%, Temperature 45°C, and NQS 6.4 × 10−3 M and interval of time 45–180s at wavelength 490 nm. The parameters used for the quantitative determinations are the reaction rate and the increase in the absorbance of the kinetic curves. This procedure has been applied to the determination of ephedrin…

Chromatographymedicine.diagnostic_testBiochemistry (medical)Clinical BiochemistryNQSBiochemistryNaphthoquinoneAnalytical ChemistryReaction rateAbsorbancechemistry.chemical_compoundSulfonatechemistrySpectrophotometryElectrochemistrymedicineDerivatizationQuantitative analysis (chemistry)SpectroscopyAnalytical Letters
researchProduct