Search results for "LIMIT"

showing 10 items of 2826 documents

Monodisperse Oligo(2,5-dipropoxy-1,4-phenyleneethynylene)s

2002

Oligo(phenyleneethynylene)s 1 are rod-like compounds with undisturbed conjugation. In supplementation of the previously described members of this series 1a−e, with repeating units of up to n = 5, this work contains the preparation of higher oligomers 1f−i (n = 6, 7, 8, 10) through the use of the Sonogashira−Hagihara reaction. Both the absorption and the fluorescence bands showed convergence for increasing values of n, reaching limiting values at the effective conjugation length of nECL = 10. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

ChemistryOrganic ChemistryDispersityPolymer chemistryLimitingPhysical and Theoretical ChemistryAbsorption (chemistry)Medicinal chemistryFluorescenceEuropean Journal of Organic Chemistry
researchProduct

Assessment of a single-acquisition imaging sequence for oxygen-sensitive (3)He-MRI.

2001

MRI of the lungs using hyperpolarized helium-3 (3He) allows the determination of intrapulmonary oxygen partial pressures (pO2). The need to separate competing processes of signal loss has hitherto required two different imaging series during two different breathing maneuvers. In this work, a new imaging strategy to measure pO2 by a single series of consecutive scans is presented. The feasibility of the method is demonstrated in three healthy human volunteers. Maps and histograms of intrapulmonary pO2 are calculated. Changes in the oxygen concentration of the inhaled gas mixture are well reproduced in the histograms. Monte Carlo (MC) simulations of the temporal evolution of 3He hyperpolariza…

ChemistryPartial PressureMonte Carlo methodHealthy subjectschemistry.chemical_elementrespiratory systemOxygenHeliumMagnetic Resonance ImagingOxygenNuclear magnetic resonanceIsotopesHistogramImage Processing Computer-AssistedHumansRadiology Nuclear Medicine and imagingLimiting oxygen concentrationComputer SimulationHyperpolarization (physics)Inhaled GasPulmonary VentilationLungMonte Carlo MethodLung functionMagnetic resonance in medicine
researchProduct

Physiologische Eigenschaften geblasener Öle

1962

Durch Blasen von polyensaure-reichen Olen bei hoheren Temperaturen erhalt man Praparate, bei denen mit zunehmender Blasintensitat die Toxicitat zunachst zunimmt, ein Maximum erreicht und dann wieder abfallt. Die Toxicitat dieser geblasenen Ole ist wahrscheinlich auf Oxypolymere zuruckzufuhren. Die Grenzdosis, von der auch mit toxischen Wirkungen solcher geblasener Ole zu rechnen ist, wurde an der Ratte zu etwa 0.45 bis 0.90 g je kg Korpergewicht bestimmt. Physiological Properties of Blown Oils By blowing oils, rich in poly-unsaturated-acids, at high temperatures a product is obtained whose toxicity is increased with increase in the intensity of blowing till a certain maximum is reached and …

ChemistryPolymer chemistryLimitingMedicinal chemistryFette, Seifen, Anstrichmittel
researchProduct

Viskosität und durchspülung von cellulosetrinitraten in aceton

1968

Die hohe Persistenzlange der Molekule von Cellulosetrinitrat (CTN) hat eine Reihe von Losungseigenschaften zur Folge, die im Lichte neuerer Theorien gut verstandlich sind: (1) Der statistische Parameter z ist niedrig, und daher ist auch in guten Losungsmitteln der Expansionsfaktor α ≡ r/rΘ nicht weit uber 1. (2) Die Durchspulbarkeit der Knauel ist hoch, das heist, der Faktor Φ = [η]M/r3 ist niedrig und hangt stark vom Molekulargewicht ab, (3) Dieser Effekt bedingt einen hohen Wert des Exponenten a in der [η]-M-Beziehung (a = 0,90 ± 0,05). The large value of the persistence length of cellulose trinitrate molecules (CTN) is responsible for a number of solution properties. A satisfactory inter…

ChemistryPolymer chemistryPhysical chemistryLimitingDie Makromolekulare Chemie
researchProduct

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
researchProduct

An in-tube SPME device for the selective determination of chlorophyll a in aquatic systems.

2010

We report a new device for the estimation of the content of chlorophyll a pigment in water samples as an indicator of water quality. The extraction of the pigment from water was also optimized. 10 mL of water was filtered through a nylon filter (45m pore size and 13 mm of diameter), after the chlorophylls were dissolved by immersing the filter in 1 mL of a low non-hazardous solvent as ethanol. An in-valve in-tube SPME device coupled to capillary liquid chromatography with diode array detection was designed. A capillary column of 70 cm in length (0.32 mm i.d. coated with 5% diphenyl–95% polydimethylsiloxane, 3m coating thickness) was used as the loop of the injection valve for preconcentrati…

Chlorophyll bDetection limitPheophytinChlorophyllQuality ControlChlorophyll aChromatographyExtraction (chemistry)Solid Phase ExtractionAnalytical chemistryPheophytinsSolid-phase microextractionAnalytical Chemistrychemistry.chemical_compoundchemistryLimit of DetectionChlorophyllSolventsSample preparationFiltrationWater Pollutants ChemicalTalanta
researchProduct

Stability of Plant Sterols in Ingredients Used in Functional Foods

2011

The content of plant sterol (PS) and their oxidation products (POPs) in eight ingredients used to enrich functional foods was studied. A gas chromatographic (GC) technique with mass-spectrometric detection was used for identification, while GC with a flame ionization detector (GC-FID) was used for quantification. β-Sitosterol was the most abundant phytosterol, and the main POPs found were derived from this compound (7α/β-hydroxysitosterol, 7-ketositosterol, and sitostanetriol). The total amount of POPs found in the ingredients ranged from 29.03 to 110.02 μg/100 g PS. The β-sitosterol oxidation rates ranged from 10 to 50 μg β-sitosterol oxides/100 g of β-sitosterol. In view of this low rate …

Chromatography GasChromatographyChemistryPhytosterolReproducibility of ResultsGeneral ChemistryPlantsMass spectrometrySterollaw.inventionSterolsIngredientFunctional FoodLimit of DetectionlawFlame ionization detectorGas chromatographyGas chromatography–mass spectrometryGeneral Agricultural and Biological SciencesOxidation-ReductionPlant sterolsJournal of Agricultural and Food Chemistry
researchProduct

Gas chromatographic analysis of resveratrol in plasma, lipoproteins and cells after in vitro incubations

1998

Resveratrol is a trihydroxystilbene present in certain red wines. It may play a role in the inhibition of lipoprotein oxidation and platelet activity. We have developed the first method to measure resveratrol in animal and human samples and to study its incorporation in vitro. After adding epicoprostanol as an internal standard, samples are subjected to lipid extraction in the presence of antioxidant and under dim light to minimize both denaturation and isomerization of the trans-resveratrol to the cis-form. Extracts were purified by cold acetone precipitation and the resveratrol-containing acetone phase was evaporated under nitrogen. The resveratrol was analyzed as a trimethylsilyl derivat…

Chromatography GasErythrocytesAntioxidantendocrine system diseasesmedicine.medical_treatmentResveratrolSensitivity and Specificitychemistry.chemical_compoundStilbenesAcetonemedicineAnimalsHumansPlatelet activationLipoprotein oxidationDetection limitChromatographyorganic chemicalsReproducibility of Resultsfood and beveragesStereoisomerismGeneral ChemistryRatsLipoproteins LDLchemistryResveratrolCalibrationLinear ModelsGas chromatographyQuantitative analysis (chemistry)Platelet Aggregation InhibitorsJournal of Chromatography B: Biomedical Sciences and Applications
researchProduct

Determination of organochlorine pesticide residues in honey from the central zone of Portugal and the Valencian community of Spain

2004

In this study nine organochlorine pesticide residues ([alpha]-, [beta]-, and [gamma]-hexachlorocyclohexane (HCH), hexachlorobenzene (HCB), aldrin, p,p'-DDE, p,p'-DDD, o,p'-DDT, and p,p'-DDT) in forty nine samples of honey collected from markets of Portugal and Spain during 2001 and 2002, respectively, were evaluated. For this evaluation, three analytical procedures were studied. The analytical procedure, based on LLE extraction with ethyl acetate followed by gas chromatography-electron-capture detection (GC-ECD) for quantification, and mass spectrometry (GC-MS) for confirmation, has been selected. Recoveries of spiked samples ranged from 68%, for [beta]-HCH, and 126% for p,p'-DDT, for forti…

Chromatography GasEthyl acetateOrganochlorineBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundElectrochemistryHydrocarbons ChlorinatedAldrinForty NinePesticidesDetection limitChromatographyPortugalPesticide residueOrganic ChemistryPesticide ResiduesReproducibility of ResultsHoneyGeneral MedicineHexachlorobenzeneReference StandardsPesticidechemistrySpainGas chromatography–mass spectrometryJournal of Chromatography A
researchProduct

Determination of 2,3,7,8-tetrachlorodibenzo-p-dioxin in goat milk and tissues by glass capillary gas chromatography and medium resolution mass fragme…

1981

Abstract An analytical method has been developed for the study of the elimination of 2,3,7,8-tetrachlodoribenzo-p-dioxin (TCDD) by lactation and its determination in various tissues of goat. The method is based on the alkaline hydrolysis of milk, liver, fat, muscle, blood, faeces and urine samples, extraction with n-hexane, treatment with sulphuric acid-saturated silica gel, chromatographic clean-up on silica gel and alumina micro-columns, and glass capillary gas chromatography—medium resolution mass fragmenography (resolution 2000). 1,2,3,4-Tetrachlorodibenzo-p-dioxin is used as the internal standard, the concentration of TCDD being determined from the calibration curve calculated from the…

Chromatography GasPolychlorinated DibenzodioxinsResolution (mass spectrometry)Calibration curveUrine010501 environmental sciencesDioxins01 natural sciencesBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundLactationmedicineAnimalsTissue Distributionheterocyclic compounds0105 earth and related environmental sciencesDetection limitReproducibilityChromatographySilica gelGoatsMuscles010401 analytical chemistryOrganic ChemistryExtraction (chemistry)General Medicine0104 chemical sciencesMilkmedicine.anatomical_structureLiverchemistryJournal of Chromatography A
researchProduct