Search results for "Fluorescence"

showing 10 items of 2463 documents

Determination of inorganic species of Sb and Te in cereals by hydride generation atomic fluorescence spectrometry

2011

A non-chromatographic fast, sensitive and easy method has been developed for the determination of Sb(III), Sb(V), Te(IV) and Te(VI) in cereal samples. The procedure is based on ultrasound assisted extraction and determination by hydride generation atomic fluorescence spectrometry (HG AFS). Preliminary studies were made in order to get the best extraction efficiency using 1 mol L-1 phosphoric acid, 1 mol L-1 nitric acid, aqua regia, 1 mol L-1 sulfuric acid and 6 mol L-1 hydrochloric acid. The extraction with aquaregia showed a clear interconversion of the species during the process, being H2SO4 the best extractant with efficiencies greater than 90% from the total content of Sb and Te quantif…

Detection limitcerealshydride generation atomic fluorescence spectrometryChemistryHydrideantimonyExtraction (chemistry)Hydrochloric acidSulfuric acidGeneral Chemistrychemistry.chemical_compoundspeciationNitric acidtelluriumAqua regiaPhosphoric acidNuclear chemistry
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Atomic fluorescence spectrometric determination of trace amounts of arsenic and antimony in drinking water by continuous hydride generation

1999

A highly sensitive and simple method has been developed for the determination of As(III), total As, Sb(III) and total Sb in drinking water samples by continuous hydride generation and atomic fluorescence spectrometry (HGAFS). For As determination, water samples aspirated in a carrier of 2 mol l(-1) HCl were merged with a reducing NaBH(4) 3%(m/v) solution, with sample and NaBH(4) flow rates of 12.5 and 1.5 ml min(-1) respectively. The hydride generated in a 170 cm reaction coil was transported to the detector with an Ar flow of 400 ml min(-1), and a limit of detection between 5 and 20 ng l(-1) was obtained. For Sb determination, 2.5 mol l(-1) HCl and 2%(m/v) NaBH(4) were employed, with respe…

Detection limitchemistryAntimonyTrace AmountsHydrideAnalytical chemistrychemistry.chemical_elementIodineAtomic fluorescence spectrometryArsenicAnalytical ChemistryVolumetric flow rateTalanta
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Chromatographic Separation of Cresol Isomers by a β‐Cyclodextrin: Application for the Determination of Volatile Phenols in Alcoholic Beverages

2006

Abstract The chromatographic separation of o‐cresol, m‐cresol, and p‐cresol by using β‐cyclodextrin as a chiral reagent has been studied. Conditions for the chromatographic separation of these isomers by using the cyclodextrin in the mobile phase or bonded in the stationary phase were optimized, and both procedures provided good results for the resolution of the chromatographic peaks. The use of fluorimetric detection (λexc 275 nm λem 300 nm) allows detection and quantification limits of the µg/L for eight studied phenols by using both procedures. The determination of volatile phenols in alcoholic beverages must be carried out using the cyclodextrin in the mobile phase because of the co‐elu…

Detection limitchemistry.chemical_classificationChromatographyCyclodextrinElutionBiochemistry (medical)Clinical BiochemistryFluorescence spectrometryCresolBiochemistryAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundchemistryReagentparasitic diseasesElectrochemistrymedicineOrganic chemistryPhenolsSpectroscopymedicine.drugAnalytical Letters
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Non-chromatographic speciation of toxic arsenic in fish

2004

Abstract A rapid, sensitive and economic method has been developed for the direct determination of toxic species of arsenic present in fish and mussel samples. As(III), As(V), dimethylarsinic acid (DMA), and monomethylarsonic acid (MMA) were determined by hydride generation–atomic fluorescence spectrometry using a series of proportional equations without the need of a chromatographic previous separation. The method is based on the extraction of arsenic species from fish through sonication with HNO3 3 mol l−1 and 0.1% (m/v) Triton and washing of the solid phase with 0.1% (m/v) EDTA, followed by direct measurement of the corresponding hydrides in four different experimental conditions. The li…

Detection limitchemistry.chemical_compoundCertified reference materialsChromatographyChemistryNitric acidSonicationExtraction (chemistry)Fluorescence spectrometrychemistry.chemical_elementSample preparationArsenicAnalytical ChemistryTalanta
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Determination of sertraline in rat plasma by HPLC and fluorescence detection and its application toin vivopharmacokinetic studies

2012

A simple, rapid, and sensitive HPLC method based on 9H-fluoren-9-ylmethyl chloroformate derivatization for the quantification of sertraline in rat plasma has been developed, requiring a plasma sample of only 0.1 mL, which was deproteinized and derivatized for 5 min in two single steps. The obtained derivative was stable at room temperature and was determined by HPLC using a fluorescence detector. The analytical column was a C(18) column and the mobile phase was acetonitrile and water (80:20, v/v). Calibration curves were linear in the range of 10-500 ng/mL. The limit of detection was approximately 3 ng/mL, and the lower limit of quantification was established at 10 ng/mL. The bias of the me…

Detection limitchemistry.chemical_compoundChromatographyPharmacokineticsChemistryCalibration curveFiltration and SeparationDerivativeChloroformateDerivatizationHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical ChemistryJournal of Separation Science
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Determination of As, Sb, Se, Te and Bi in milk by slurry sampling hydride generation atomic fluorescence spectrometry

2003

A simple and fast analytical procedure has been developed for the determination of As, Sb, Se, Te and Bi in milk samples by hydride generation atomic fluorescence spectrometry (HG-AFS). Samples were treated with aqua regia for 10min in an ultrasound water bath and pre-reduced with KBr for total Se and Te determination or with KI and ascorbic acid for total As and Sb, the determination of Bi being possible in all with or without pre-reduction. Slurries of samples, in the presence of antifoam A, were treated with NaBH(4) in HCl medium to obtain the corresponding hydrides, and AFS measurements were processed in front of external calibrations prepared and measured in the same way as samples. Re…

Detection limitchemistry.chemical_compoundchemistryHydrideRelative standard deviationSlurryAnalytical chemistryAqua regiaChemical elementAscorbic acidAtomic fluorescence spectrometryAnalytical ChemistryTalanta
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Klimt artwork: red-pigment material investigation by backscattering Fe-57 Mössbauer spectroscopy, SEM and p-XRF

2017

Material tests were performed on a rediscovered Klimt-artwork "Trompetender Putto". We performed studies on the red colored spots, mainly taken from non-restored parts. MIMOS II Fe-57 Mossbauer spectroscopy (novelty in art-pigment analysis) mainly reveals haematite and crystallized goethite in red colors. Electron microscopy can identify various layers of the original and overpainting of an artwork. The number of layers fluctuates between three and four chemically painted areas. The portable X-ray fluorescence analysis enables to reduce the pigment list to containing mercury (cinnabar), lead, zinc, iron and titanium. Infrared-light-irradiation visualizes the different age of the pigments.

Dewey Decimal Classification::500 | Naturwissenschaften::540 | ChemieArcheologyGoethiteMaterials scienceScanning electron microscopepigmentsAnalytical chemistryinfra-red-light investigationchemistry.chemical_elementZinc01 natural sciencesKlimt: “Trompetender Putto”PigmentMaterialcharakterisierung0103 physical sciencesMössbauer spectroscopy0601 history and archaeologyddc:750lcsh:CC1-960010306 general physics060102 archaeologyTrompetender PuttoMössbauer spectroscopy06 humanities and the artsDewey Decimal Classification::700 | Künste Bildende Kunst allgemein::750 | MalereiOverpaintingKlimt GustavDewey Decimal Classification::700 | Künste Bildende Kunst allgemeinCinnabarchemistryPigmentvisual_artddc:540visual_art.visual_art_mediumddc:660lcsh:ArchaeologyX-ray fluorescence analysisddc:700660 Technische Chemiescanning electron microscopyTitanium
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POLYASPARTAMIDE-POLYLACTIDE GRAFT COPOLYMERS WITH TUNABLE PROPERTIES FOR THE REALIZATION OF FLUORESCENT NANOPARTICLES FOR IMAGING

2015

Here, the synthesis and the characterization of novel amphiphilic graft copolymers with tunable properties, useful in obtaining polymeric fluorescent nanoparticles for application in imaging, are described. These copolymers are obtained by chemical conjugation of rhodamine B (RhB) moieties, polylactic acid (PLA), and O-(2-aminoethyl)-O'-methyl poly(ethylene glycol) (PEG) on α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA). In particular, PHEA is first functionalized with RhB to obtain PHEA-RhB with a derivatization degree in RhB (DDRhB ) equal to 0.55 mol%. By varying the reaction conditions, different amounts of PLA are grafted on PHEA-RhB to obtain PHEA-RhB-PLA with DDPLA equal to 1.9, 4…

Diagnostic ImagingMaterials sciencePolymers and Plasticspolyethylene glycol (PEG)PolymersPolyestersNanoparticlemacromolecular substancesPolyethylene Glycolschemistry.chemical_compoundstomatognathic systemPolylactic acidAmphiphilePolymer chemistryPEG ratioMaterials ChemistryCopolymerRhodamine BLactic AcidPolyhydroxyethyl Methacrylateαβ-poly-(N-2-hydroxyethyl)-dl-aspartamide (PHEA)polylactic acid (PLA)nanoparticleOrganic Chemistrytechnology industry and agricultureFluorescencechemistryNanoparticlesfluorescenceEthylene glycol
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Expression of P, S, and F1C adhesins by cytotoxic necrotizing factor1-producing Escherichia coli from septicemic and diarrheic pigs

1997

Nineteen papC-positive cytotoxic necrotizing factor 1 (CNF1)-producing Escherichia coli isolates from pigs with septicemia or diarrhea were tested for the presence of pap-, sfa-, and afa-related sequences encoding P/Prs, S/F1C, and Dr/AFA adhesins respectively. Production of adhesins by isolates was tested by mannose-resistant hemagglutination (MRHA), sialidase treatment of erythrocytes and particle agglutination tests. Production of P, S, and F1C fimbriae by isolates was also examined by immunofluorescence. All isolates were pap+ by PCR. Eighteen isolates (95%) were MRHA for ovine and human A erythrocytes and exhibited GalNac-GalNac receptor specificity associated with class III P(Prs) adh…

DiarrheaSerotypeErythrocytesHemagglutinationSwine[SDV]Life Sciences [q-bio]Bacterial ToxinsFimbriaBiologyImmunofluorescencemedicine.disease_causeMicrobiologyMicrobiologyAgglutination TestsSepsisEscherichia coliGeneticsmedicineAnimalsHumansAdhesins BacterialMolecular BiologyEscherichia coliEscherichia coli InfectionsSwine DiseasesAntiserumSheepmedicine.diagnostic_testCytotoxinsEscherichia coli Proteinsbiochemical phenomena metabolism and nutritionBacterial adhesin[SDV] Life Sciences [q-bio]Agglutination (biology)Fimbriae BacterialCattle
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The importance of a highly active and DeltapH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cyc…

2005

The present study focuses on the regulation of diatoxanthin (Dtx) epoxidation in the diadinoxanthin (Ddx) cycle containing algae Phaeodactylum tricornutum, Thalassiosira pseudonana, Cyclotella meneghiniana and Prymnesium parvum and its significance for the control of the photosystem II (PS II) antenna function. Our data show that Dtx epoxidase can exhibit extremely high activities when algal cells are transferred from high light (HL) to low light (LL). Under HL conditions, Dtx epoxidation is strongly inhibited by the light-driven proton gradient. Uncoupling of the cells during HL illumination restores the high epoxidation rates observed during LL. In Ddx cycle containing algae, non-photoche…

DiatomsPhotosystem IIbiologyLightPhysiologyZeaxanthin epoxidaseAlgal ProteinsDiadinoxanthinDiatoxanthinEukaryotaPhotosystem II Protein ComplexPlant ScienceHydrogen-Ion ConcentrationXanthophyllsPhotochemistrychemistry.chemical_compoundchemistryPhotoprotectionbiology.proteinElectrochemical gradientChlorella vulgarisOxidoreductasesAgronomy and Crop ScienceChlorophyll fluorescenceViolaxanthinJournal of plant physiology
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