Search results for "FT-IR"

showing 10 items of 48 documents

FT-IR spectroscopy : A powerful tool for studying the inter- and intraspecific biodiversity of cultivable non-Saccharomyces yeasts isolated from grap…

2016

International audience; The efficiency of the FT-IR technique for studying the inter- and intra biodiversity of cultivable non-Saccharomyces yeasts (NS) present in different must samples was examined. In first, the capacity of the technique FF-IR to study the global diversity of a given sample was compared to the pyrosequencing method, used as a reference technique. Seven different genera (Aureobasidium, Candida, Cryptococcus, Hanseniaspora, Issatchenkia, Metschnikowia and Pichia) were identified by FT-IR and also by pyrosequencing. Thirty-eight other genera were identified by pyrosequencing, but together they represented less than 6% of the average total population of 6 musts. Among the sp…

0301 basic medicineIdentification[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionBiodiversityWineHanseniasporaSaccharomycesMicrobial ecology[ SDV.MP ] Life Sciences [q-bio]/Microbiology and ParasitologyYeastsSpectroscopy Fourier Transform InfraredVitisDNA FungalMycological Typing TechniquesPhylogenyCandidaIntragenomic variationbiologySp-nov.Pyrolysis mass-spectrometryPyrosequencingBiodiversityCandida zemplininaYeast in winemaking[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyFT-IR spectroscopyMetschnikowiaAlcoholic fermentationMicrobiology (medical)food.ingredientWine yeast030106 microbiologyMicrobiologyIntraspecific competitionCandida-zemplininaSaccharomyces03 medical and health sciencesfoodBotanyRNA Ribosomal 18SMolecular BiologyBase SequenceComputational BiologySequence Analysis DNAbiology.organism_classificationGreen lacewingsStrain typingPyrosequencingTransform-infrared-spectroscopy[SDV.AEN]Life Sciences [q-bio]/Food and NutritionBotrytis-affected wine
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Physico-chemical investigation of the state of cyanamide confined in AOT and lecithin reversed micelles

2004

Sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and lecithin reversed micelles containing cyanamide have been investigated by small-angle X-ray scattering, FT-IR, and 1H NMR spectroscopy at various cyanamide-to-surfactant molar ratio (X) and at fixed surfactant concentration (0.1 mol kg-1). Experimental data are consistent with a model of cyanamide molecules confined in reversed micelles, quite uniformly distributed among them and mainly located among surfactant headgroups. SAXS data analysis leads also to hypothesize a unidimensional growth of the reversed micelles with increasing the X value. Moreover, the cyanamide state and the cyanamide/cyanamide interactions in reversed micelles have bee…

1h nmr spectroscopyfood.ingredientSodiumASSEMBLIESchemistry.chemical_elementMicelleLecithinSurfaces Coatings and FilmsFT-IRchemistry.chemical_compoundfoodAEROSOL-OTchemistrySOLVATION DYNAMICSMICROEMULSIONSMaterials ChemistryNANOPARTICLESOrganic chemistryCyanamidePhysical and Theoretical ChemistryACETAMIDENuclear chemistrySettore CHIM/02 - Chimica Fisica
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Preparation and structural characterization of organotin(IV) complexes with ligands containing a hetero {N} atom and a hydroxy group or hydroxy and c…

2005

AbstractTwenty-two n-butyltin(IV) and t-butyltin(IV) complexes of ligands containing an –OH (–C@O) group or –OH and –COOHgroups and an aromatic {N} donor atom were prepared by metathetical reactions. On the basis of the FT-IR and Mo¨ssbauer spec-troscopic data, molecular structures were assigned to these compounds. The binding sites of the ligands were identified by means ofFT-IR spectroscopic measurements, and it was found that in most cases the organotin(IV) moiety reacts with the phenolic form ofthese ligands. In the complexes with –OH and –COOH functions, the –COOH group is coordinated to the organotin(IV) centres in amonodentate manner. The 119 Sn Mo¨ssbauer and the FT-IR studies suppor…

2-MERCAPTOPYRIDINEStereochemistryMossbauer spectroscopyMETAL COMPLEXESchemistry.chemical_elementorganotin(IV)3-HYDROXYPYRIDINEBiochemistryMedicinal chemistryInorganic Chemistry2-HYDROXYPYRIDINEGroup (periodic table)Mössbauer spectroscopyMaterials ChemistryMoietyCRYSTAL-STRUCTURERAMAN-SPECTRAPhysical and Theoretical ChemistryBinding siteFourier transform infrared spectroscopyChemistryOrganic ChemistryX-ray diffraction DICARBOXYLIC-ACIDSFT-IRMODELTrigonal bipyramidal molecular geometryTINSettore CHIM/03 - Chimica Generale E InorganicaX-ray crystallographyTinOrganotin(IV)FT-IRMössbauer spectroscopyX-ray diffractionJournal of Organometallic Chemistry
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Effect of Organic Amendments on the Evolution of Soil Organic Matter in Soils Stressed by Intensive Agricultural Practices

2013

Losses of soil organic carbon often occur because of intensive agricultural practices that lead to removal of organic carbon following harvest production and to insufficient inputs. Organic amendments can be a very appropriate matrix for enhancing organic carbon content in very stressed agricultural soils. In general, they, enhancing soil organic matter, play an important role in environmental matrices due, for example, to their capacity in retaining water, in interacting with organic and inorganic pollutants, and in enhancing nutrient availability to plants. For this reason, the understanding of the mechanisms with which organic amendments interact with other chemicals in the environment i…

AgroforestryChemistrybusiness.industrySoil organic matterSettore AGR/13 - Chimica AgrariaOrganic ChemistryAmendements FFC-NMR relaxometry FT-IR Humic acids NMR soil orgaqnic matterhumic acidNMRFT-IRAgronomyFFC-NMR relaxometryAgriculturesoil organic matterSoil waterAmendmentbusiness
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Photoactivity of Nanostructured TiO2 Catalysts in Aqueous System and their Surface Acid-Base, Bulk and Textural Properties

2007

This work reports on the characterisation and determintion of the photocatalytic activity of some TiO2 catalysts prepared using TiCl4 as precursor. The samples, consisting of suspensions, dispersions or powders of nanonstructured anatase or rutile phases, were obtained in very mild conditions, i.e., by boiling the solution obtained after hydrolysis of TiCl4 at atmospheric pressure: it is worth noting that no calcination was necessary to obtain photoactive phases. The samples were characterised by X-ray diffraction (XRD), determination of the BET specific surface area (SSA), scanning electron microscopy (SEM) observations and diffuse reflectance spectroscopy (DRS). FT-IR spectroscopy was use…

AnataseAqueous solutionMaterials scienceDiffuse reflectance infrared fourier transformScanning electron microscopeAnalytical chemistryFT-IR characterisationGeneral Chemistrylaw.inventionPhotocatalysiChemical engineeringlawSpecific surface areananostructured TiO2PhotocatalysisCalcinationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiephotodegradationPhotodegradation
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Preparation and structural studies on dibutyltin(IV) complexes with pyridine mono- and dicarboxylic acids

2004

Abstract A number of organotin(IV) complexes with pyridine mono- and dicarboxylic acids (containing ligating –COOH group(s) and aromatic {N} atoms) were prepared in the solid state. The bonding sites of the ligands were determined by means of FT-IR spectroscopic measurements. It was found that in most cases the –COO− groups form bridges between two central {Sn} atoms, thereby leading to polymeric (oligomeric) complexes. On this basis, the experimental 119Sn Mossbauer spectroscopic data were treated with partial quadrupole splitting approximations. The calculations predicted the existence of complexes with octahedral (oh) and trigonal-bipyramidal (tbp) structures, but the formation of comple…

ChemistryCrystal structureOrganic ChemistryInorganic chemistrySolid-stateQuadrupole splittingCrystal structureBiochemistryOrganotin(IV) compoundFT-IRM€ossbauerInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronGroup (periodic table)Mössbauer spectroscopyPyridineMaterials ChemistryNMR studiesPhysical and Theoretical ChemistryFourier transform infrared spectroscopyJournal of Organometallic Chemistry
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New Alternative in the Methodology of Extraction and Dyeing with Active Molecules Derived from Vegetal Sources

2016

Abstract The general objective of this study refers to the identification of a sustainable and physical methodology of extraction of active compounds, envisaging the preservation of the high purity active natural dye molecule from nut shell (juglone), even under the conditions of an extraction performed in a mixt solvent medium (water-ethanol). The second major objective of the study consists of the application of these above mentioned dyes onto natural and synthetic substrates, thus making a correlation between their colour attributes and the fibrous composition of the substrates they are applied on. The motivation of this research was given by the identification of an improved extraction …

ChromatographyChemistryExtraction (chemistry)green walnut shellsjugloneInfrared spectroscopy04 agricultural and veterinary sciences040401 food scienceHigh-performance liquid chromatographySolventchemistry.chemical_compound0404 agricultural biotechnologyFT-RAMAN.FT-IR spectroscopyGeneral Earth and Planetary SciencesOrganic chemistryMoleculeUS extractioncoloristic attributeDyeingNatural dyeJugloneGeneral Environmental ScienceProcedia Technology
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Premature aging in bone of fish from a highly polluted marine area

2015

Fish species have attracted considerable interest in studies assessing biological responses to environmental contaminants. In this study, the attention has been focussed on fishbone of selected fish species from a highly polluted marine area, Augusta Bay (Italy, Central Mediterranean) to evaluate if toxicant elements had an effect on the mineralogical structure of bones, although macroscopic deformations were not evident. In particular, an attempt was made to evaluate if bone mineral features, such as crystallinity, mineral maturity and carbonate/phosphate mineral content, determined by XR-Diffraction and FT-IR Spectroscopy, suffered negative effects due to trace element levels in fishbone,…

ChromiumMediterranean climatePremature agingAugusta Bay (Italy)XRDMineralogyAquatic ScienceOceanographyBone and Boneschemistry.chemical_compoundCalcification PhysiologicX-Ray DiffractionSpectroscopy Fourier Transform InfraredAnimalsBone mineralMaturity (geology)Body WeightWater PollutionFishesTrace elementCrystalline structure fishboneReproducibility of ResultsAging PrematureMercuryContaminationPollutionHydroxylapatiteFT-IRItalychemistryEnvironmental chemistryTrace elementEnvironmental scienceCarbonateBay
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Confinement of chiral molecules in reverse micelles: FT-IR, polarimetric and VCD investigation on the state of dimethyl tartrate in sodium bis(2-ethy…

2008

Abstract The state of d and l -dimethyl tartrate confined within dry sodium bis(2-ethylhexyl) sulfosuccinate (AOT) reverse micelles dispersed in CCl 4 has been investigated by FT-IR spectroscopy, polarimetry, and vibrational circular dichroism (VCD). Measurements have been performed at 25 °C as a function of the solubilizate-to-surfactant molar ratio ( R ) at a fixed AOT concentration (0.158 M). The analysis of experimental data is consistent with the hypothesis that both enantiomers of dimethyl tartrate are mainly entrapped in the reverse micelles and located in proximity to the surfactant head-group region. The formation of this interesting self-organized chiral nanostructure involves som…

Circular dichroismInorganic chemistryInfrared spectroscopyTartrateMicellechemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPulmonary surfactantVibrational circular dichroismPhysical chemistryEnantiomerDimethyl tartrate Sodium bis(2-ethylhexyl) sulfosuccinate Reverse micelles Chiral nanostructures FT-IR spectroscopy Vibrational circular dichroism Optical rotationColloids and Surfaces A: Physicochemical and Engineering Aspects
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Preparation and structural studies on diorganotin(IV) complexes of N-nitroso-N-phenylhydroxylaminates

2007

Abstract Diorganotin(IV)-complexes of the N -nitroso- N -phenylhydroxylaminates (hereinafter cupf), Et 2 Sn(cupf) 2 ( 1 ), Bu 2 Sn(cupf) 2 ( 2 ), {[Bu 2 Sn(cupf)] 2 O} 2 ( 3 ), t -Bu 2 Sn(cupf) 2 ( 4 ) and Oc 2 Sn(cupf) 2 ( 5 , 6 ) were prepared and characterised by FT-IR and Mossbauer spectroscopic measurements. The binding modes of the ligand were identified by FT-IR spectroscopy, and it was found that the ligand is coordinated in chelating or bridging mode to the organotin(IV) center. The 119 Sn Mossbauer and FT-IR studies support the formation of trans -O h ( 1 – 6 ) structures. The X-ray diffraction analysis of 4 revealed that the tin centre is in a skew-trapezoidal geometry defined by…

CupferronChemistryLigand1HOrganic Chemistrychemistry.chemical_elementNitrosoBiochemistryX-ray diffractionFT-IRMossbauerInorganic ChemistryCrystallographychemistry.chemical_compound13C and 119Sn NMR spectroscopyMössbauer spectroscopyX-ray crystallographyMaterials ChemistryCupferronChelationPhysical and Theoretical ChemistryTinSpectroscopyDiorganotin(IV)Journal of Organometallic Chemistry
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