Search results for "REAGENT"

showing 10 items of 699 documents

Selective recovery of phosphorus as AlPO4 from silicon-free CFB-derived fly ash leachate

2018

The prospect of phosphorus (P) recovery from siliceous fly ash was investigated. The phosphorus content in the pristine fly ash was 1.21%. Obtaining pure phosphorus products from fly ash is very challenging because of high concentration of other elements, silicon (Si) at 17.3% being the major contaminant. The fly ash was fractionated with sieve size of 125 μm to concentrate the phosphorus in the small-size fraction, which also facilitated the removal of 78% of silica (Si) in the solid phase. The fractionated fly ash was treated with 8 M HCl in order to remove 98% of Si by aging (5 h) of leachate until precipitation of Si-gel, and a phosphorus-rich solution is obtained. Iron (Fe) is also con…

AlPO4 precipitationpiiSilicon020209 energyphosphorus recoverychemistry.chemical_elementrauta02 engineering and technology010501 environmental sciencesRaw material01 natural sciencescomplex mixturesIndustrial and Manufacturing EngineeringironImpurity0202 electrical engineering electronic engineering information engineeringMaterials Chemistryrecovery (recapture)lentotuhkaLeachatephosphorusta116ta215fosfori0105 earth and related environmental sciencesPrecipitation (chemistry)Fe-EDTA chelationPhosphorusfungiMetals and Alloyssiliconfly ashfly ash utilizationchemistrytalteenottoReagentFly asherottaminen (tekniikka)Nuclear chemistry
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Synthesis of terpenoid unsaturated 1,4-dialdehydes. Pi-facial selectivity in the Diels-Alder reaction of the 1-vinyl-2-methylcyclohexene moiety of po…

2000

AldehydesVinyl CompoundsMolecular StructureChemistryAcetyleneTerpenesOrganic ChemistryMolecular ConformationTerpenoidAlkynesMoietyOrganic chemistryIndicators and ReagentsSelectivityDiels–Alder reactionThe Journal of organic chemistry
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Catalytic Enantioselective Aza-Reformatsky Reaction with Cyclic Imines

2016

A catalytic highly enantioselective aza-Reformatsky reaction with cyclic aldimines and ketimines for the synthesis of chiral b-amino esters with good yields and excellent enantioselectivities is reported.Areadily available diaryl prolinol is used as a chiral ligand, ZnMe2 as a zinc source and ethyl iodoacetate as reagent in the presence of air atmosphere. The reaction with cyclic ketimines generates a quaternary stereocenter with excellent levels of enantioselectivity. Furthermore, five-membered N-sulfonyl ketimines were used as electrophiles with good enantiomeric excesses, under the optimized reaction conditions. Moreover, several chemical transformations were performed with the chiral b-…

AldimineEthyl iodoacetateBeta-amino ester010402 general chemistry01 natural sciencesCatalysisReaccions químiquesStereocenterchemistry.chemical_compoundCatàlisiAsymmetric catalysisOrganic chemistryheterocyclic compoundsReformatsky reactionchemistry.chemical_classification010405 organic chemistryOrganic ChemistryChiral ligandEnantioselective synthesisGeneral Chemistry0104 chemical sciencesProlinolCyclic ketiminesZincchemistryReformatsky reactionFISICA APLICADAReagentQuímica orgànicaChemistry - A European Journal
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Caracterización de barita cubana y su reducción carbotérmica en horno de microondas

2007

The Cuban Barite (BaSO4) is characterized by X ray diffraction, chemical analysis and scanning electron microscopy. The principal components are identified and its characteristic morphology is shown. Its carbothermic reduction under microwave irradiation is carried out with the purpose of to improve the yield of this stage during the mineral transformation process in reagent of barium of diverse applications. La barita cubana (BaSO4) se ha caracterizado por difracción de rayos X, análisis químico y microscopía electrónica de barrido. Se han identificado sus componentes mayoritarios y así mismo se muestra su morfología característica. Se ha realizado su reducción carbotérmica en horno de mic…

Alkaline earth metalChemistryScanning electron microscopeMetals and AlloysBarium sulfidechemistry.chemical_elementMineralogyBariumMicrowave assisted reductionCondensed Matter PhysicsBaritachemistry.chemical_compoundBariteReducción asistida por microondasReagentMicroscopyX-ray crystallographyMicrowave irradiationMaterials ChemistryBarium sulfideReducción carbotérmicaSulfuro de barioCarbothermic reductionPhysical and Theoretical ChemistryNuclear chemistry
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Alkylation at the active site of the D-3-hydroxybutyrate dehydrogenase (BDH), a membrane phospholipid-dependent enzyme, by 3-chloroacetyl pyridine ad…

1997

The structure of the rat liver's D-3-hydroxybutyrate dehydrogenase (BDH) active site has been investigated using an affinity alkylating reagent, the 3-chloroacetyl pyridine adenine dinucleotide (3-CAPAD). This NAD+ analogue reagent strongly inactivates the enzyme following a concentration- and time-dependent process with a stoichiometry of approximately 1. The reagent reacts at the coenzyme binding site as revealed by the efficient protection by NADH. The effect of 3-CAPAD is stronger with the enzyme into its natural membrane environment than with the lipid-free purified apoBDH or with the reconstituted apoBDH-mitochondrial phospholipid complex. The pH-dependent effect on the inactivation p…

AlkylationStereochemistryAffinity labelMitochondria LiverDehydrogenaseBiochemistryHydroxybutyrate DehydrogenaseMembrane LipidsAnimalsCoenzyme bindingCysteineBinding sitePhospholipidsBinding SitesAffinity labelingMolecular StructurebiologyChemistryActive siteAffinity LabelsGeneral MedicineNADRatsReagentLinear Modelsbiology.proteinNAD+ kinaseBiochimie
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P-Chirogenic Phosphines Supported by Calix[4]arene: New Insight into Palladium-Catalyzed Asymmetric Allylic Substitution

2013

The first P-chirogenic mono- and diphosphine ligands supported on the upper rim of a calix[4]arene moiety were synthesized using the ephedrine methodology. The lithiated calix[4]arene mono- and dianions both react with the oxazaphospholidine–borane, prepared from ephedrine, to afford regio- and stereoselectively the corresponding calix[4]arenyl aminophosphine–boranes, by cleavage of the heterocyclic ring at the P–O bond position. Subsequent reactions with HCl and then organolithium reagent and finally decomplexation with DABCO lead to the corresponding calix[4]arenyl mono- or diphosphines. Both enantiomers of the calix[4]arenyl phosphines were obtained either by using (+)- or (−)-ephedrine …

Allylic rearrangementStereochemistryOrganic Chemistrychemistry.chemical_elementDABCOBoraneOrganolithium reagentMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryDiphosphinesMoietyPhysical and Theoretical ChemistryEnantiomerPalladiumOrganometallics
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ChemInform Abstract: Photoinduced Molecular Rearrangements. The Photochemistry of Some 1,2, 4-Oxadiazoles in the Presence of Nitrogen Nucleophiles. F…

2010

The photochemistry of some 3,5-disubstituted 1,2,4-oxadiazoles in the presence of nitrogen nucleophiles [external, such as added amines or hydrazines, or internal, such as an o-aminophenyl moiety at C(3) of the oxadiazole ring] has been investigated. In the irradiation of 5-amino-(or 5-N-substituted amino) 3-phenyl-1,2,4-oxadiazoles in the presence of aliphatic primary amines (or ammonia), photolytic species arising from heterolytic cleavage of the ring O−N bond capture the nucleophilic reagent to give open-chain intermediates, which develop into 1,2,4-triazolin-5-ones. Similarly, irradiations of 3,5-diphenyl-, 3-methoxy-5-phenyl-, and 5-methyl-3-phenyl-1,2,4-oxadiazoles gave 1,2,4-triazole…

Ammoniachemistry.chemical_compoundchemistryNucleophileReagentOxadiazoleMoietyContext (language use)General MedicineRing (chemistry)PhotochemistryHeterolysisChemInform
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High-pressure flow-injection assembly. Indirect determination of glycine by atomic absorption spectrometry.

1991

A procedure for the determination of glycine is described. The method is based on the reaction of the analyte with finely powdered, solid copper(II) carbonate in a continuous-flow assembly. The optimum experimental conditions of pH, temperature, sample volume, flow-rate, column length and internal diameter, and the linear range of calibration, were studied. Interference from foreign substances that accompany this amino acid in pharmaceutical formulations was studied, and the method was applied to the determination of glycine.

AnalyteAnalytical chemistryGlycinechemistry.chemical_elementBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawElectrochemistryCalibrationEnvironmental ChemistrySpectroscopychemistry.chemical_classificationChromatographyChemistrySpectrophotometry AtomicTemperatureHydrogen-Ion ConcentrationCopperAmino acidLinear rangeGlycineCarbonic AcidCarbonateIndicators and ReagentsAtomic absorption spectroscopyThe Analyst
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Selective determination of trimethylamine in air by liquid chromatography using solid phase extraction cartridges for sampling.

2004

Abstract The selective determination of trimethylamine (TMA) in air by liquid chromatography is reported. Sampling is effected by flushing air through C18-packed solid-phase extraction (SPE) cartridges at a flow rate of 15 mL/min for 15 min. Next, TMA is desorbed from the cartridges and injected into the chromatographic system. The analyte is then selectively retained on a precolumn ( 20 mm ×2.1 mm i.d., packed with 30 μm, Hypersil C18 phase), and derivatized on-line by injecting 9-fluorenylmethyl chloroformate (FMOC). Finally, the TMA-FMOC derivative is transferred to the analytical column ( 125 mm ×4 mm i.d., LiChrospher 100 RP18, 5 μm), and monitored at 262 nm. The method was applied to …

AnalyteAnalytical chemistryTrimethylamineChloroformateAir Pollutants OccupationalBuffersBiochemistryAnalytical ChemistryCartridgechemistry.chemical_compoundMethylaminesBoric AcidsSolid phase extractionDetection limitReproducibilityChromatographyOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineReference StandardsSolutionschemistryCalibrationIndicators and ReagentsSpectrophotometry UltravioletChromatography Liquid
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Application of solid-phase microextraction combined with derivatization to the determination of amphetamines by liquid chromatography

2004

This work evaluates the utility of solid-phase microextraction (SPME) in the analysis of amphetamines by liquid chromatography (LC) after chemical derivatization of the analytes. Two approaches have been tested and compared, SPME followed by on-fiber derivatization of the extracted amphetamines, and solution derivatization followed by SPME of the derivatives formed. Both methods have been applied to measure amphetamine (AP), methamphetamine (MA), and 3,4-methylenedioxymethamphetamine (MDMA), using the fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC) and carbowax-templated resin (CW-TR)-coated fibers. Data on the application of the proposed methods for the analysis of different kin…

AnalyteAqueous solutionChromatographyChemistryMicrochemistryAmphetaminesExtraction (chemistry)BiophysicsReproducibility of ResultsCell BiologyChloroformateSolid-phase microextractionSensitivity and SpecificityBiochemistryMatrix (chemical analysis)chemistry.chemical_compoundReference ValuesReagentDerivatizationMolecular BiologyChromatography High Pressure LiquidAnalytical Biochemistry
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