Search results for "SPECTROSCOPY"

showing 10 items of 10293 documents

FT-IR quantitative analysis of solvent mixtures by the constant ratio method

1999

Abstract An analytical methodology to quantify compounds in complex mixtures by FTIR spectroscopy is proposed and the “Constant Ratio Method” (CRM) was developed. The addition of a standard to the sample allows us to establish a constant KMS characteristic of the Analyte/Standard system which can be employed as a quantification factor of the analyte in different samples . In the proposed method the measurements are independent of optical path length. This method has been successfully applied to quantify butylacetate and toluene in binary and tertiary samples and tertiary mixtures. Butylacetate/toluene/nujol have been resolved employing valeronitrile as standard, obtaining values for relativ…

AnalyteChemistryOrganic ChemistryAnalytical chemistryTolueneAnalytical ChemistryInorganic ChemistrySolventchemistry.chemical_compoundNujolFourier transform infrared spectroscopyConstant (mathematics)Quantitative analysis (chemistry)SpectroscopyOptical path lengthJournal of Molecular Structure
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Automated Photo-Induced Fluorescence Determination of Flumetsulam

2009

The present article deals with a new procedure for determination of the herbicide flumetsulam. The fluorimetric procedure is performed on the basis of photo-increased fluorimetric emission of the pesticide solution and by means of a multicommutation continuous-flow assembly. The alkaline solution containing the analyte is irradiated online and then directly forced through the fluorimeter flow cell. The analysis of different samples is completely automated, as the analyte separation was performed online by including a separation cartridge in the manifold. When dealing with solid samples (such as soil samples), the automation was completed by adding to the manifold the corresponding device fo…

AnalyteChromatographyAqueous solutionChemistryBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Fluorescence spectrometryAnalytical chemistryBiochemistryFluorescenceAnalytical ChemistryCartridgeFluorometerElectrochemistrySample preparationSpectroscopyAnalytical Letters
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Analytical capabilities of high performance liquid chromatography – Atmospheric pressure photoionization – Orbitrap mass spectrometry (HPLC-APPI-Orbi…

2015

A new analytical method was established and validated for the analysis of 27 brominated flame retardants (BFRs), including so called "emerging" and "novel" BFRs (EBFRs and NBFRs) in fish samples. High performance liquid chromatography (HPLC) coupled to Orbitrap mass spectrometry (Orbitrap-MS) employing atmospheric pressure photoionization (APPI) interface operated in negative mode was used for the identification/quantitation of contaminants. HPLC-Orbitrap-MS analysis provided a fast separation of selected analytes within 14 min, thus demonstrating a high throughput processing of samples. The developed methodology was tested by intralaboratory validation in terms of recovery, repeatability, …

AnalyteChromatographyAtmospheric pressureChemistryAnalytical chemistryRepeatabilityMass spectrometryOrbitrapBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionPolybrominated diphenyl ethersCertified reference materialslawEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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In-tube solid phase microextraction coupled to miniaturized liquid chromatography for both, noble metal nanoparticle assessment and sensitive plasmon…

2021

Abstract Colorimetric localized surface plasmon resonance (LSPR) as analytical response is applied for a wide number of chemical sensors and biosensors. However, the dependence of different factors, such as size distribution of nanoparticles (NPs), shape, dielectric environment, inter-particle distance and matrix, among others, can provide non-reliable results by UV–vis spectrometry in complex matrices if NP assessment is not carried out, particularly at low levels of analyte concentrations. Miniaturized liquid chromatography, capillary (CapLC) and nano (NanoLC), coupled on line with in-tube solid phase microextraction (IT-SPME) is proposed for the first time for both, controlling suitabili…

AnalyteChromatographyChemistry010401 analytical chemistryNanoparticle02 engineering and technologyengineering.material021001 nanoscience & nanotechnologyMass spectrometrySolid-phase microextraction01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryMatrix (chemical analysis)engineeringEnvironmental ChemistryNoble metalSurface plasmon resonance0210 nano-technologyBiosensorSpectroscopyAnalytica chimica acta
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Evaluation and elimination of the blank bias error using the H-point standard additions method (HPSAM) in the simultaneous spectrophotometric determi…

1997

Abstract The aim of this report is to demonstrate the usefulness of the HPSAM in all instances where the determination of two analytes requires the use of an absorbent reagent, particularly when it does not present a constant analytical signal because of its consumption. This problem can be treated as a ternary mixture by the HPSAM method and then, the fundamentals of the method for resolving these kind of mixtures can be applied. The method can calculate the concentration of one species from spectral data at two wavelengths where the two other species present the same absorbance relationship. These wavelength pairs are easily found, and can be selected to give the most precise results. The…

AnalyteChromatographyChemistryAnalytical chemistryArsenazo IIIBiochemistrySpectral lineAnalytical ChemistryAbsorbanceStandard additionReagentCalibrationEnvironmental ChemistryTernary operationSpectroscopyAnalytica Chimica Acta
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Procedure for automated background correction in flow systems with infrared spectroscopic detection and changing liquid-phase composition

2009

This paper describes a partial least squares (PLS) based automatic procedure to correct for changes in the spectral contribution of the solvent or solvent mixtures from solute spectra recorded in these solvents. The procedure was developed for successful on-line Fourier transform infrared (FT-IR) detection in gradient high-performance liquid chromatography (HPLC) separations. It requires a reference FT-IR data set containing all possible combinations of the expected variation in solvent composition. Furthermore, a spectral region ( A) in these spectra is required where the solvents show absorption but the analytes do not. This is the case for the system ACN:H2O, an often-applied solvent mi…

AnalyteChromatographyChemistryAnalytical chemistryInfrared spectroscopyMass spectrometryHigh-performance liquid chromatographyChemometricssymbols.namesakeFourier transformColumn chromatographysymbolsFourier transform infrared spectroscopyInstrumentationSpectroscopy
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Control of matrix interferences by multiple linear regression models in the determination of arsenic and lead concentrations in fly ashes by inductiv…

2010

A multiple linear regression technique was used to evaluate and correct the matrix interferences in the determination of As and Pb concentrations in fly ashes by inductively coupled plasma optical emission spectrometry. The direct determination of As and Pb in SRM 1633b by ICP-OES failed to obtain the certified concentrations, except in a couple of cases. However, it proved possible to use the multiple linear regression (MLR) technique to correct the determined concentrations to a satisfactory level. This method of correction is based on the multiple regression line obtained from the analysis of 19 synthetic mixtures of matrix and analyte elements (Al, As, Ca, Fe, Pb, and Si) at five concen…

AnalyteChromatographyChemistryAnalytical chemistrychemistry.chemical_elementPlasmaAnalytical ChemistryMatrix (chemical analysis)Fly ashStandard additionLinear regressionInductively coupled plasmaSpectroscopyArsenicJournal of Analytical Atomic Spectrometry
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Identification and determination of synthetic cannabinoids in herbal products by dry film attenuated total reflectance-infrared spectroscopy.

2017

A new procedure has been developed for the identification and quantitative determination of synthetic cannabinoids in illicit herbal preparations. The methodology is based on the use of attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) measurement of sample extracts with 2-propanol drying 5µL of the extracts onto the ATR crystal. The qualitative identification was carried out on the 2-propanol extract after identification of the herbal matrix, followed by its subtraction and using a cut-off criterion of 75%. Quantitative determination was made by univariate calibration using the absorbance of the band located at 1520cm-1 of the spectrum. Four different cannabin…

AnalyteChromatographyChemistryCannabinoidsPlant Extracts010401 analytical chemistryInfrared spectroscopy01 natural sciences0104 chemical sciencesAnalytical ChemistryMatrix (chemical analysis)Absorbance03 medical and health sciences0302 clinical medicineAttenuated total reflectionSynthetic cannabinoidsCalibrationSpectroscopy Fourier Transform InfraredmedicineCalibration030216 legal & forensic medicineFourier transform infrared spectroscopymedicine.drugTalanta
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Flow-injection spectrofluorimetric determination of paracetamol

1990

Abstract A flow-injection spectrofluorimetric determination of paracetamol is reported, based on the oxidation of the analyte with potassium hexacyanoferrate(III) immobilized on an anion-exchange resin, the fluorescence being enhanced with N,N′-dimethylformamide. Concentrations of paracetamol in the range 0.04–17.60 mg l−1 are determined with a relative standard deviation of 1.5%. The injection rate is 25 samples h−1. The influence of foreign species and the determination of paracetamol in several pharamaceutical formulations are also reported.

AnalyteChromatographyChemistryPotassiumdigestive oral and skin physiologyRelative standard deviationFluorescence spectrometrychemistry.chemical_elementInjection rateBiochemistryAnalytical ChemistryEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Determination of aliphatic amines in water by liquid chromatography using solid-phase extraction cartridges for preconcentration and derivatization

2001

Bond Elut C18 solid-phase extraction cartridges were used for preconcentration and pre-column derivatization with 3,5-dinitrobenzoyl chloride (DNB) of aliphatic amines in water. Conditions for analyte preconcentration and derivatization (including the volume of sample, concentration of reagent, time of reaction and pH) were investigated, using ethylamine, isopropylamine and dimethylamine as model compounds. On the basis of these studies, a rapid and sensitive method for the determination of aliphatic amines in water is presented. The analytes are retained and purified on the cartridges and then derivatized and desorbed by drawing in succession the DNB solution and acetonitrile. The collecte…

AnalyteChromatographyElutionReproducibility of ResultsBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochemistryHumansEnvironmental ChemistrySolid phase extractionIsopropylamineAminesEthylamineDerivatizationAliphatic compoundDimethylamineWater Pollutants ChemicalSpectroscopyChromatography LiquidThe Analyst
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