Search results for "CHEMICAL FRACTIONATION"

showing 10 items of 54 documents

Aqueous enzymatic process assisted by microwave extraction of oil from yellow horn (Xanthoceras sorbifolia Bunge.) seed kernels and its quality evalu…

2013

Abstract In this study, aqueous enzymatic process (AEP) assisted by microwave extraction (ME) of oil from yellow horn ( Xanthoceras sorbifolia Bunge.) seed kernel was investigated. Central composite design (CCD) and response surface methodology (RSM) were used to optimise an enzyme cocktail (cellulase, hemicellulase, pectinase) for AEP. The main factors of ME were also studied. A maximal oil extraction yield of 55.8% was achieved under optimal conditions. Moreover, scanning electron microscope (SEM) was applied to characterise the extraction process. Analysing chemical composition of the extracted oil by GC–MS showed that the content of unsaturated fatty acids by this emerging method (91.18…

Quality ControlChromatographyAqueous solutionCentral composite designbiologyGlycoside HydrolasesChemistryExtraction (chemistry)General MedicineCellulaseChemical FractionationGas Chromatography-Mass SpectrometryAnalytical ChemistrySapindaceaeYield (chemistry)Seedsbiology.proteinPlant OilsResponse surface methodologyPectinaseMicrowavesChemical compositionFood ScienceFood chemistry
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Characterization of the alcoholic fraction of vegetable oils by derivatization with diphenic anhydride followed by high-performance liquid chromatogr…

2008

Abstract Aliphatic and triterpene alcohols present in vegetable oils have been identified and determined by HPLC using UV–vis and MS detection after previous derivatization with diphenic anhydride. The alcoholic fraction was obtained by saponification, extraction and TLC (according to the European Union official procedure). Derivatization was performed in tetrahydrofuran in the presence of suspended grinded urea, which increases the reaction rate and yield. Derivatized extracts were chromatographed on a C8 column using gradient elution with acetonitrile/water mixtures containing 0.1% acetic acid, with UV–vis followed by negative-ion mode MS detection. Using linear discriminant analysis of t…

Resolution (mass spectrometry)Fraction (chemistry)Chemical FractionationSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryAcetic acidchemistry.chemical_compoundPlant Oilsmedia_common.cataloged_instanceEuropean unionDerivatizationChromatography High Pressure Liquidmedia_commonChromatographyEsterificationOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineModels ChemicalchemistryAlcoholsMultivariate AnalysisDibenzoxepinsSaponificationJournal of Chromatography A
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Tuning the surface of nanoparticles: Impact of poly(2-ethyl-2-oxazoline) on protein adsorption in serum and cellular uptake

2016

Item does not contain fulltext Due to the adsorption of biomolecules, the control of the biodistribution of nanoparticles is still one of the major challenges of nanomedicine. Poly(2-ethyl-2-oxazoline) (PEtOx) for surface modification of nanoparticles is applied and both protein adsorption and cellular uptake of PEtOxylated nanoparticles versus nanoparticles coated with poly(ethylene glycol) (PEG) and non-coated positively and negatively charged nanoparticles are compared. Therefore, fluorescent poly(organosiloxane) nanoparticles of 15 nm radius are synthesized, which are used as a scaffold for surface modification in a grafting onto approach. With multi-angle dynamic light scattering, asym…

SerumTime FactorsPolymers and PlasticsSurface PropertiesNanoparticleBioengineeringProtein Corona02 engineering and technologyChemical Fractionation010402 general chemistry01 natural sciencesCell LineBiomaterialschemistry.chemical_compoundAdsorptionDynamic light scatteringMaterials ChemistryPolyaminesOrganic chemistryHumanspoly(2-ethyl-2-oxazoline)Particle SizeElectrophoresis Agar Gelpoly(ethylene glycol)RhodaminesProteinscellular uptake021001 nanoscience & nanotechnologyprotein adsorptionDynamic Light ScatteringEndocytosis0104 chemical scienceschemistryChemical engineeringSurface modificationNanomedicineInstitut für ChemienanoparticlesAdsorption0210 nano-technologyEthylene glycolNanomedicine Radboud Institute for Molecular Life Sciences [Radboudumc 19]BiotechnologyProtein adsorption
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The organic carbon derived from sewage sludge as a key parameter determining the fate of trace metals.

2007

8 pages; International audience; In a sandy agricultural soil of south-west of France, continuously cultivated with maize and amended with sewage-sludge over 20 years, the behavior of three trace metals (Cu, Pb, and Zn) was studied during the sludge applications (1974-1993) and after its cessation (1993-1998). Using the delta13C analysis, the dynamics of different sources of organic matter were followed in order to elucidate the influence of the sludge-derived organic matter on the fate of trace metals in the soil and its particle size fractions. This study revealed that sludge-derived organic matter contributed to the formation of macroaggregates through the binding of preexisting microagg…

Sewage-sludgeHealth Toxicology and Mutagenesis010501 environmental sciencesChemical FractionationMESH : Carbon01 natural sciencesMESH : Soil Pollutants[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryMESH : Particle SizeSoil PollutantsTotal organic carbonchemistry.chemical_classificationCarbon IsotopesParticle-size fractionsSewage04 agricultural and veterinary sciencesGeneral MedicineMESH: Metals HeavyPollutionSoil contamination6. Clean water[ SDE.MCG ] Environmental Sciences/Global ChangesEnvironmental chemistryMESH : Metals HeavyFranceValorisationMESH : Carbon IsotopesMESH: Nitrogen IsotopesMESH : FertilizersEnvironmental Engineering[SDE.MCG]Environmental Sciences/Global Changesd13CAmendment[ SDV.SA.SDS ] Life Sciences [q-bio]/Agricultural sciences/Soil studychemistry.chemical_elementMESH: CarbonZincMESH: Fertilizers[SDV.SA.SDS]Life Sciences [q-bio]/Agricultural sciences/Soil studyMESH: Chemical FractionationTrace metalsMetals HeavyEnvironmental ChemistryOrganic matterMESH: Particle SizeParticle SizeMESH : FranceFertilizersOrganic carbonMESH: Sewage0105 earth and related environmental sciencesMESH : Nitrogen IsotopesMESH: Soil PollutantsNitrogen IsotopesMESH : Chemical FractionationPublic Health Environmental and Occupational HealthEnvironmental engineeringMESH: Carbon IsotopesGeneral ChemistryBiodegradation[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/Geochemistry[SDE.ES]Environmental Sciences/Environmental and SocietyCarbonMESH: FrancechemistryMESH : Sewage040103 agronomy & agriculture0401 agriculture forestry and fisheriesSludge[ SDE.ES ] Environmental Sciences/Environmental and Society
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A Simple Entropic-Driving Separation Procedure of Low-Size Silver Clusters, Through Interaction with DNA

2021

Abstract Synthesis and purification of metal clusters without strong binding agents by wet chemical methods are very attractive for their potential applications in many research areas. However, especially challenging is the separation of uncharged clusters with only a few number of atoms, which renders the usual techniques very difficult to apply. Herein, we report the first efficient separation of Ag2 and Ag3 clusters using the different entropic driving forces when such clusters interact with DNA, into which Ag3 selectively intercalates. After sequential dialysis of the samples and denaturalizing the DNA‐Ag3 complex, pure Ag2 can be found in the dialysate after extensive dialysis. Free Ag…

SilverResearch areasEntropyDna interactionIntercalation (chemistry)silver clustersMetal NanoparticlesChemical Fractionationchemistry.chemical_compoundseparation proceduresQD1-999Strong bindingmass spectrometryChemistryCommunicationentropically-driven processesGeneral ChemistryDNAIntercalating AgentsCommunicationsDNA interactionChemistryChemical physicsSettore CHIM/03 - Chimica Generale E InorganicaDialysis (biochemistry)DNAMetal clustersSeparation procedure
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Determination at low ppm levels of dithiocarbamate residues in foodstuff by vapour phase-liquid phase microextraction-infrared spectroscopy

2010

Abstract A methodology based on the vapour phase (VP) generation of carbon disulphide from non-volatile dithiocarbamate compounds has been developed for determination of pesticide residues in foodstuff at low ppm levels. The method involves a selective reaction combined with liquid phase microextraction (LPME) and transmission infrared measurements. The use of a home made transmission cell improved the detection limits (LOD) compared to the use of attenuated total reflectance measurements by a factor of approximately 80. Using the most appropriate experimental conditions for the CS2 generation and LPME preconcentration, the precision of the methodology, expressed as the relative standard de…

ZinebDetection limitchemistry.chemical_classificationResidue (complex analysis)ChromatographySpectrophotometry InfraredChemistryPesticide ResiduesAnalytical chemistryInfrared spectroscopyChemical FractionationMass spectrometryBiochemistryEthylenebis(dithiocarbamates)Gas Chromatography-Mass SpectrometryAnalytical ChemistryLimit of DetectionAttenuated total reflectionManebEnvironmental ChemistryGas chromatographyGas chromatography–mass spectrometryDithiocarbamateFood AnalysisSpectroscopyAnalytica Chimica Acta
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Analytical comparison and sensory representativity of SAFE, SPME, and Purge and Trap extracts of volatile compounds from pea flour

2012

Pisum sativum is of great economic and nutritional interest due to its protein content. Nevertheless, pea products are underused as a protein source in human food because of their strong beany flavour. Therefore, the objective of this study was to select an efficient and representative method to extract volatile molecules of pea flour. In the first step, three extraction methods were chosen: solid phase micro extraction (SPME); Purge and Trap extraction and solvent assisted flavour evaporation (SAFE). The corresponding extracts were analysed by gas chromatography coupled with mass spectrometry. In the second step, the sensory representativity of the extracts was assessed either by direct ga…

[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionFlourFlavourChemical FractionationMass spectrometry01 natural sciencesGas Chromatography-Mass SpectrometryAnalytical ChemistryPurge and trapsafe0404 agricultural biotechnologyHumansSolid Phase Micro Extractiondirect gas chromatography-olfactometrypisum sativum2. Zero hungerVolatile Organic CompoundsChromatographyChemistrySolid Phase Extraction010401 analytical chemistryExtraction (chemistry)Peas04 agricultural and veterinary sciencesGeneral Medicine040401 food science0104 chemical sciencessensory representativitySolventpurge and trapTastespmeGas chromatographyGas chromatography–mass spectrometry[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood ScienceFood Chemistry
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Modelling hydrolysis: Simultaneous versus sequential biodegradation of the hydrolysable fractions

2018

Hydrolysis is considered the limiting step during solid waste anaerobic digestion (including co-digestion of sludge and biosolids). Mechanisms of hydrolysis are mechanistically not well understood with detrimental impact on model predictive capability. The common approach to multiple substrates is to consider simultaneous degradation of the substrates. This may not have the capacity to separate the different kinetics. Sequential degradation of substrates is theoretically supported by microbial capacity and the composite nature of substrates (bioaccessibility concept). However, this has not been experimentally assessed. Sequential chemical fractionation has been successfully used to define i…

[SDV.BIO]Life Sciences [q-bio]/BiotechnologyBiosolidsSEQUENTIAL EXTRACTIONANAEROBIC DIGESTIONBIODEGRADATION02 engineering and technology010501 environmental sciencesTRITICUM AESTIVUM01 natural sciences7. Clean energyNUMERICAL MODELSLUDGE DIGESTIONBioreactorsMETHANEBIOLOGICAL MATERIALSACTIVATED SLUDGE0202 electrical engineering electronic engineering information engineeringAnaerobiosisSequential modelPRIORITY JOURNALWaste Management and DisposalComputingMilieux_MISCELLANEOUSCALIBRATIONSewageCONCENTRATION (PARAMETER)ChemistryFRACTIONATIONACID HYDROLYSISINCUBATION TIMEMODELLINGHYDROLYSISCHEMICAL FRACTIONATIONSEQUENTIAL DEGRADATIONBiodegradation EnvironmentalWASTE TREATMENTORGANIC MATTER[SDE]Environmental SciencesANAEROBIC DIGESTION MODELADM1SOLID WASTE020209 energyMODELSFractionationCAPACITYHydrolysisDIGESTIONISOTOPIC FRACTIONATIONNONHUMANCHEMICAL OXYGEN DEMANDARTICLEMODEL SELECTION0105 earth and related environmental sciencesChromatographyModels TheoreticalSUBSTRATESBiodegradationSIMULTANEOUS DEGRADATIONHOMOGENEOUS MATERIALSAnaerobic digestionWASTE WATER MANAGEMENTActivated sludgeAPPLEDegradation (geology)Waste Management
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Typology of exogenous organic matters based on chemical and biochemical composition to predict potential nitrogen mineralization

2010

Our aim was to develop a typology predicting potential N availability of exogenous organic matters (EOMs) in soil based on their chemical characteristics. A database of 273 EOMs was constructed including analytical data of biochemical fractionation, organic C and N, and results of N mineralization during incubation of soil–EOM mixtures in controlled conditions. Multiple factor analysis and hierarchical classification were performed to gather EOMs with similar composition and N mineralization behavior. A typology was then defined using composition criteria to predict potential N mineralization. Six classes of EOM potential N mineralization in soil were defined, from high potential N minerali…

[SDV.BIO]Life Sciences [q-bio]/Biotechnologygenetic structures010501 environmental sciences01 natural sciencesMinéralisationBiochemical compositionOrganic ChemicalsWaste Management and DisposalHigh potentialhttp://aims.fao.org/aos/agrovoc/c_35657chemistry.chemical_classificationMineralsChemistry04 agricultural and veterinary sciencesGeneral MedicineComposition chimiqueClassificationhierarchical classificationDisponibilité d'élément nutritifCycle de l'azoteEnvironmental chemistryhttp://aims.fao.org/aos/agrovoc/c_5193http://aims.fao.org/aos/agrovoc/c_1794AlgorithmsP33 - Chimie et physique du solBiochemical fractionationEnvironmental EngineeringNitrogenhttp://aims.fao.org/aos/agrovoc/c_7170Mineralogybiochemical fractionationBioengineeringhttp://aims.fao.org/aos/agrovoc/c_27938FractionationTeneur en azoten mineralizationMatière organique du solhttp://aims.fao.org/aos/agrovoc/c_5268Fertilité du solMultiple factor analysisOrganic matterComputer SimulationNitrogen cycle0105 earth and related environmental sciencesRenewable Energy Sustainability and the EnvironmentP35 - Fertilité du sol[ SDV.BIO ] Life Sciences [q-bio]/BiotechnologyMineralization (soil science)eye diseasesAmendement organiqueModels Chemical040103 agronomy & agriculture0401 agriculture forestry and fisheriessense organsexogenous organic mattertypologyhttp://aims.fao.org/aos/agrovoc/c_12965http://aims.fao.org/aos/agrovoc/c_1653http://aims.fao.org/aos/agrovoc/c_15999F04 - Fertilisation
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Isotope Fractionation of Selenium During Fungal Biomethylation by Alternaria alternata

2011

The natural abundance of stable Se isotopes may reflect sources and formation conditions of methylated Se. We aimed at (1) quantifying the degree of methylation of selenate [Se(VI)] and (hydro)selenite [Se(IV)] by the fungus Alternaria alternata at pH 4 and 7 and (2) determining the effects of these different Se sources and pH values on 82Se/76Se ratios (δ82/76Se) in methylselenides. Alternaria alternata was incubated with Se(VI) and Se(IV) in closed microcosms for 11-15 days and additionally with Se(IV) for 3-5 days at 30 °C. We determined Se concentrations and δ82/76Se values in source Se(VI) and Se(IV), media, fungi, and trapped methylselenides. In Se(VI) incubations, methylselenide vola…

biologyIsotopeAlternariachemistry.chemical_elementGeneral ChemistryMethylationFungi imperfectiFractionationChemical Fractionationbiology.organism_classificationMethylationAlternaria alternataSelenateTrace ElementsSeleniumchemistry.chemical_compoundIsotope fractionationIsotopeschemistryEnvironmental chemistryEnvironmental ChemistryBiotransformationSeleniumEnvironmental Science & Technology
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