Search results for "Chemical Analysis"

showing 10 items of 324 documents

Sodium nitrate and tungsten as matrix modifiers for the determination of arsenic in shotgun pellets by electrothermal atomic absorption spectrometry

2001

A method for the determination of arsenic in a complicated sample matrix by Zeeman effect electrothermal atomic absorption spectrometry using tungsten and sodium nitrate as matrix modifiers was developed. The determination of arsenic in SRM C2416 (Bullet Lead) and SRM 2710 (Montana Soil) by ETAAS using a mixture of palladium and magnesium nitrate as a matrix modifier failed to obtain the certified concentrations at the 95% level of confidence using the t-test. Both tungsten and sodium nitrate as matrix modifiers stabilized arsenic so that the certified concentrations of the SRMs were determined with high accuracy and precision (RSD   0.999), with low detection and quantification limits, wer…

ChemistryAnalytical chemistryPelletschemistry.chemical_elementTungstenAnalytical Chemistrylaw.inventionMatrix (chemical analysis)Magnesium nitratechemistry.chemical_compoundlawSodium nitrateStandard additionAtomic absorption spectroscopySpectroscopyArsenicJ. Anal. At. Spectrom.
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Chronological development of element concentrations in grapes during growth and ripeness and during fermentation of must determined by instrumental n…

2014

Abstract The chronological development of element concentrations during growth and ripeness of grapes described in the literature has only been concerned with the macro elements Mg, K, and Ca. Concentrations of trace elements in must are only described as a snapshot at the end of the ripeness. Therefore, the motivation for the present work was to accompany the growth and the ripening process of grapes successively by systematically determining element concentrations in grapes of Riesling and Cabernet Sauvignon by neutron-activation analyses. While for a number of elements, the concentrations in the grapes increased as a function of grape development (e.g., Na, K, Rb, Al), other concentratio…

ChemistryNondestructive analysisFermentationFood scienceRadiochemical analysisPhysical and Theoretical ChemistryNeutron activation analysisRipenessNeutron temperatureNeutron activationRadiochimica Acta
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Using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for the characterization of functionalized carbon nanotubes

2013

RATIONALE Functionalization of carbon nanotubes (CNTs) generates complex systems that require the development of suitable characterization protocols. New techniques have been explored, and existing analytical and spectroscopic methods to characterize functionalized CNTs have been adapted. Presently, chemical characterization of functionalized CNTs (f-CNTs) remains a difficult task. METHODS Matrix-assisted laser desorption/ionization (MALDI) analysis is performed on f-MWCNT samples prepared via grafting or absorption of anti-oxidant (AO) molecules on both MWCNT-COOH and MWCNT-OH. Covalently functionalized MWCNTs were subjected to thermal degradation and/or hydrolysis reaction before analysis…

ChemistryOrganic ChemistryAnalytical chemistryCarbon nanotubeMass spectrometryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)AdsorptionChemical engineeringlawDesorptionSurface modificationMoleculeAbsorption (chemistry)SpectroscopyRapid Communications in Mass Spectrometry
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CsPbCl3 nanocrystals dispersed in the Rb0,8Cs0,2Cl matrix studied by far-infrared spectroscopy

2009

Abstract The comparative far-infrared spectroscopy studies of Rb0.8Cs0.2Cl and Rb0.8Cs0.2Cl containing CsPbCl3 nanocrystals between 170 and 320 K are reported. The effect of cesium lead chloride nanocrystals on the phonon modes of the host matrix, particularly manifested in different temperature behavior of LO–TO splitting and the temperature dependence of high frequency dielectric constant, are demonstrated.

ChemistryPhononLead chlorideAnalytical chemistrychemistry.chemical_elementGeneral ChemistryDielectricCondensed Matter PhysicsMatrix (chemical analysis)NanocrystalCaesiumFar infrared spectroscopyMaterials ChemistrySpectroscopySolid State Communications
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Preparation and characterization of organofunctionalized bentonite clay bearing aminophosphonic groups in heavy metal uptake

2019

Abstract Bentonite (Bnt) with covalently immobilized N-propylaminodi(methylenephosphonic) groups (Bnt-ADPA) was obtained through a two-step synthesis including aminosilanization and phosphorylation of resulting aminobentonite through Moedritzer-Irani reaction. The grafting of an aminosilane layer in the interplanar space of the bentonite was investigated by XRD, and the presence of N and P-containing groups was confirmed by FTIR, 31P and 29Si MAS NMR. The immobilization of the organic functional groups increased the interplanar distance in bentonite matrix at 52% that essentially improved filtration properties compared to raw bentonite. The number of surface acid groups was evaluated to 0.8…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solution02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyGrafting01 natural sciencesPollutionMatrix (chemical analysis)MetalAdsorptionCovalent bondvisual_artBentonitevisual_art.visual_art_mediumChemical Engineering (miscellaneous)Fourier transform infrared spectroscopy0210 nano-technologyWaste Management and Disposal0105 earth and related environmental sciencesNuclear chemistryJournal of Environmental Chemical Engineering
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An overview of the analytical methods for the determination of organic ultraviolet filters in biological fluids and tissues.

2012

Organic UV filters are chemical compounds added to cosmetic sunscreen products in order to protect users from UV solar radiation. The need of broad-spectrum protection to avoid the deleterious effects of solar radiation has triggered a trend in the cosmetic market of including these compounds not only in those exclusively designed for sun protection but also in all types of cosmetic products. Different studies have shown that organic UV filters can be absorbed through the skin after topical application, further metabolized in the body and eventually excreted or bioaccumulated. These percutaneous absorption processes may result in various adverse health effects, such as genotoxicity caused b…

Chemistrymedicine.disease_causeBiochemistryAnalytical ChemistryBody FluidsMatrix (chemical analysis)Adverse health effectEnvironmental chemistryPercutaneous absorptionmedicineBiological fluidsEnvironmental ChemistryAnimalsHumansSample preparationTissue DistributionOrganic ChemicalsSpectroscopyGenotoxicityUltravioletVolume concentrationAnalytica chimica acta
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On-line gradient liquid chromatography–Fourier transform infrared spectrometry determination of sugars in beverages using chemometric background corr…

2008

Abstract An on-line gradient reversed phase liquid chromatography–Fourier transform infrared spectrometry (LC–FTIR) method was developed for the determination of fructose, glucose, sucrose and maltose in beverages. Improved chromatographic resolution was obtained using a linear gradient from 75 to 55% (v/v) acetonitrile in water in 15 min. Changes in the background spectra were corrected employing “univariate background correction based on the use of a reference spectra matrix” (UBC-RSM) and using the ratio of absorbance (AR) at 2256 and 2253 cm −1 for the identification of the eluent spectra within the RSM. The method provided limits of detection in the order of 0.75 mg ml −1 . The precisi…

ChemometricsMatrix (chemical analysis)Detection limitColumn chromatographyChromatographyResolution (mass spectrometry)ChemistryAnalytical chemistryInfrared spectroscopyReversed-phase chromatographyFourier transform spectroscopyAnalytical ChemistryTalanta
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Atomic Absorption Spectrophotometric Determination of Cobalt in Foods

1985

A method is reported for determination of chromium in foodstuffs. Organic matter is digested with nitric acid, followed by oxidation to Cr(VI) and extraction with methyl isobutyl ketone (MIBK) after HCl addition. Chromium determinations are performed by flame absorption spectroscopy. Absence of interferences is verified and recovery tests are performed on food samples. Quantitation limit (3.8 ng/mL), accuracy (NBS Standard Reference Material 1,573 Tomato Leaves, 4,500 +/- 500 ng/g, found 3,860 +/- 409 ng/g), and precision (CV for vegetable matrix = 9.05%, CV for animal matrix = 14.95%) of the procedure are evaluated.

ChromatographyAbsorption spectroscopymedicine.diagnostic_testChemistryExtraction (chemistry)Analytical chemistrychemistry.chemical_elementGeneral Chemistrylaw.inventionMatrix (chemical analysis)Methyl isobutyl ketonechemistry.chemical_compoundChromiumlawNitric acidSpectrophotometrymedicineAtomic absorption spectroscopyJournal of AOAC INTERNATIONAL
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On-line Chloride Interference Removal for Arsenic Determination in Waste Water and Urine by ICP-MS Using a Modified Capillary

2002

The determination of arsenic in environmental samples like waste waters from industrial effluents and in biological samples like urine is very important due to the toxic nature of some of its species at moderate levels of exposure. The objective of this study was to evaluate the capability of modified anionic capillaries to remove chloride for ICP-MS determination of arsenic, which causes spectral interference due to formation of 40 Ar 35 Cl + . Also high chloride content gives non-spectral interferences. The results indicate that arsenic at a concentration higher than 1 µg L m 1 in a matrix with a chloride content up to 600 mg L m 1 can be accurately determined using a 3-aminopropyltrimeth…

ChromatographyCapillary actionHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthSoil Sciencechemistry.chemical_elementUrinePollutionChlorideAnalytical ChemistryMatrix (chemical analysis)chemistryWastewatermedicineEnvironmental ChemistryWaste Management and DisposalEffluentInductively coupled plasma mass spectrometryArsenicWater Science and Technologymedicine.drugInternational Journal of Environmental Analytical Chemistry
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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
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