Search results for "Partial"

showing 10 items of 1477 documents

Orbital-Resolved Partial Charge Transfer from the Methoxy Groups of Substituted Pyrenes in Complexes with Tetracyanoquinodimethane—A NEXAFS Study

2012

It is demonstrated that the near-edge X-ray absorption fine structure (NEXAFS) provides a powerful local probe of functional groups in novel charge transfer (CT) compounds and their electronic properties. Microcrystals of tetra-/hexamethoxypyrene as donors with the strong acceptor tetracyano-p-quinodimethane (TMP/HMP-TCNQ) were grown by vapor diffusion. The oxygen and nitrogen K-edge spectra are spectroscopic fingerprints of the functional groups in the donor and acceptor moieties, respectively. The orbital selectivity of the NEXAFS pre-edge resonances allows us to precisely elucidate the participation of specific orbitals in the charge transfer process. Upon complex formation, the intensit…

ChemistryResonanceGeneral ChemistryPhotochemistryBiochemistryAcceptorTetracyanoquinodimethaneCatalysisXANESSpectral linechemistry.chemical_compoundPartial chargeColloid and Surface ChemistryAtomic orbitalSelectivityJournal of the American Chemical Society
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Influence of gel composition in the synthesis of MoVTeNb catalysts over their catalytic performance in partial propane and propylene oxidation

2010

[EN] MoVTeNb mixed oxides catalysts have been prepared by a slurry method with different molar compositions (Mo/Te ratio from 2 to 6 and Nb/(V + Nb) ratio from 0 to 0.7) in the synthesis gel leading to different crystalline phases distribution and catalytic behaviour in the partial oxidation of both propane and propylene to acrylic acid. Chemical analysis indicates that the composition of samples before and after the heat-treatment changes, especially the Te-content, since a significant amount of Te is lost during the heat-treatment step when the amount of oxalate (from niobium oxalate) increases in the synthesis gel. Thus, the nature of the crystalline phases and the catalytic performance …

ChemistryStereochemistryOxalic acidAcroleinGeneral ChemistryCatalysisOxalateCatalysisPropeneAcrylic acidMo–V–Te–Nb–O mixed oxideschemistry.chemical_compoundLoss of telluriumChemical engineeringPropaneOxalic acidPartial oxidationSelective propane oxidationAcrylic acid
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Evaluation of infrared spectroscopy as a screening tool for serum analysis

2013

Abstract The application of attenuated total reflectance Fourier transform infrared (ATR-FT-IR) spectroscopy to the determination of clinical parameters in serum using partial least squares (PLS) has been evaluated as a point-of-care diagnostic tool. In this study the effect of using an increased size of the calibration set and the influence of the origin of samples and their interyear variation on the prediction capability of the method were considered. PLS-ATR-FT-IR provides a green, fast and cheap point-of-care tool for the determination of total protein. Albumin, glucose, urea, HDL, LDL and total cholesterol were predicted with relative errors between 15 and 32%. The analytical predicti…

ChemometricsAnalyteStandard errorChemistryCalibration (statistics)Attenuated total reflectionPrincipal component analysisPartial least squares regressionStatisticsSample (statistics)SpectroscopyAnalytical ChemistryMicrochemical Journal
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Quantitative determination of surface area of silica gel particles by near infrared spectroscopy and chemometrics

2008

Abstract Surface areas of silica gel particles have been quantitatively determined by using near infrared spectrometry and chemometrics. Surface areas of six silica gel samples with varying surface area (300–750 m2/g) have been determined by the common Brunauer–Emmett–Teller (BET) method and used in preparing mixtures of silica gel samples with varying surface area in the ranges 300–474 and 500–750 m2/g. The near infrared spectra of the mixtures were measured and the spectral profiles calibrated against the calculated surface area of the mixtures as dependent variable using partial least squares (PLS) technique. The models obtained from the calibrations were then used in predicting the surf…

Chemometricschemistry.chemical_compoundColloid and Surface ChemistryChemistrySilica gelNear-infrared spectroscopyPartial least squares regressionAnalytical chemistryCalibrationParticleInfrared spectroscopyBET theoryColloids and Surfaces A: Physicochemical and Engineering Aspects
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Spatio-temporal dynamics of a planktonic system and chlorophyll distribution in a 2D spatial domain: matching model and data

2017

AbstractField data on chlorophyll distribution are investigated in a two-dimensional spatial domain of the Mediterranean Sea by using for phytoplankton abundances an advection-diffusion-reaction model, which includes real values for physical and biological variables. The study exploits indeed hydrological and nutrients data acquired in situ, and includes intraspecific competition for limiting factors, i.e. light intensity and phosphate concentration. As a result, the model allows to analyze how both the velocity field of marine currents and the two components of turbulent diffusivity affect the spatial distributions of phytoplankton abundances in the Modified Atlantic Water, the upper layer…

Chlorophyll0301 basic medicineChlorophyll aScienceSpatial ecology; Marine ecosystems; Phytoplankton dynamics; Partial differential equationsAtmospheric sciencesArticlePhosphates03 medical and health scienceschemistry.chemical_compoundSpatio-Temporal AnalysisMediterranean seaWater columnPhytoplanktonMediterranean SeaMarine ecosystemSpatial ecologySeawaterTransectPhytoplankton dynamicMultidisciplinaryEcologyChlorophyll AQTemperatureRModels TheoreticalPlanktonPartial differential equationsSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Light intensity030104 developmental biologychemistryChlorophyllPhytoplanktonMedicineEnvironmental scienceSeasonsScientific Reports
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Visible-light driven oxidation of gaseous aliphatic alcohols to the corresponding carbonyls via TiO2 sensitized by a perylene derivative

2013

Sensitized P25 TiO2 was prepared by wet impregnation with a home-prepared perylene dye, i.e., N,N?-bis(2-(1- piperazino)ethyl)-3,4,9,10-perylene-tetracarboxylic acid diimide dichloride (PZPER). Energy levels of PZPER were found to be compatible with those of TiO2 allowing fast electron transfer. The obtained catalyst has been characterized and used in the gas-phase partial oxidation of aliphatic primary and secondary alcohols, i.e., methanol, ethanol, and 2- propanol. The reaction was carried out under cut-off (?> 400 nm) simulated solar radiation in O2 atmosphere. The perylene derivative allowed a good absorbance of visible radiation thanks to its low optical energy gap (2.6 eV) which was …

Chromatography GasLightHealth Toxicology and MutagenesisInorganic chemistryFormaldehydeElectronsPhotochemistry..ImidesCatalysisCatalysischemistry.chemical_compoundDiimideEnvironmental ChemistryReactivity (chemistry)Partial oxidationVisible light photocatalysisPeryleneTitaniumSettore ING-IND/24 - Principi Di Ingegneria ChimicaMolecular StructureMethanolPerylene-sensitized TiO2General MedicinePollutionAliphatic alcohol oxidationchemistryYield (chemistry)MethanolPerylene-sensitized TiO2 Visible light photocatalysis Aliphatic alcohol oxidationOxidation-ReductionPerylene
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Finding the best separation in situations of extremely low chromatographic resolution.

2010

Abstract Samples with a large number of compounds or similarities in their structure and polarity may yield insufficient chromatographic resolution. In such cases, however, finding conditions where the largest number of compounds appears sufficiently resolved can be still worthwhile. A strategy is here reported that optimises the resolution level of chromatograms in cases where conventional global criteria, such as the worst resolved peak pair or the product of elementary resolutions, are not able to detect any separation, even when most peaks are baseline resolved. The strategy applies a function based on the number of “well resolved” peaks, which are those that exceed a given threshold of…

Chromatography Reverse-PhaseChromatographyAcetonitrilesResolution (mass spectrometry)ChemistryLow resolutionOrganic ChemistrySeparation (aeronautics)Analytical chemistryGeneral MedicineFunction (mathematics)Partial resolutionHydrogen-Ion ConcentrationBiochemistryAnalytical ChemistryChromatographic separationModels ChemicalYield (chemistry)Organic ChemicalsJournal of chromatography. A
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Partial least squares attenuated total reflectance IR spectroscopy versus chromatography: the greener method

2012

Method election is a complex task that must be done carefully in order to ensure the capability of analytical methodologies to provide appropriate data for problem solving. This is a real challenge in all fields, but especially with bioanalysis, which in many cases involves the need to do a large number of determinations in complex

ChromatographyBioanalysisChromatographyChemistryClinical BiochemistryInfrared spectroscopyGreen Chemistry TechnologyGeneral MedicineAnalytical ChemistryMedical Laboratory TechnologyAttenuated total reflectionSpectroscopy Fourier Transform InfraredPartial least squares regressionLeast-Squares AnalysisGeneral Pharmacology Toxicology and PharmaceuticsBioanalysis
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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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Direct determination of Mancozeb by photoacoustic spectrometry

2006

Abstract A solvent free, fast and environmentally friendly photoacoustic-infrared-based methodology (PAS-FTIR) was developed for the determination of Mancozeb in agrochemicals. This methodology was based on the direct measurement of the transmittance spectra of solid samples and a multivariate calibration model to determine the active ingredient concentration. The proposed partial least squares (PLS) model was made using nine standards prepared by mixing different amounts of kaolin and Mancozeb, with concentrations between 5.43 and 88.10% (w/w). A hierarchical cluster analysis was made in order to classify the samples in terms of similarity in the PAS-FTIR spectra. From their spectra differ…

ChromatographyChemistryDirect methodAnalytical chemistryPhotoacoustic imaging in biomedicineMass spectrometryBiochemistryAnalytical Chemistrychemistry.chemical_compoundPartial least squares regressionCalibrationEnvironmental ChemistryMancozebSample preparationMetalaxylSpectroscopyAnalytica Chimica Acta
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