Search results for "Reagent"

showing 10 items of 699 documents

Biobased Epoxy Resin by Electrochemical Modification of Tall Oil Fatty Acids

2019

A biobased epoxy resin was prepared from tall oil fatty acids (TOFAs), a byproduct of the pulping industry. As free carboxylic acids compromise resin stability, TOFA was subjected to non-Kolbe decarboxylation to give alkenes upon loss of CO2. Thereby, the degree of unsaturation is significantly increased. This electrosynthetic protocol using an undivided cell setup and inexpensive graphite electrodes in a galvanostatic operation mode was scaled to a 1.5 L reactor, making use of electric current as a green and waste-free reagent. Simple, cost-efficient epoxidation using oxone subsequently gives an epoxy resin of low viscosity. Curing with anhydrides yields thermoset materials. Dynamic mechan…

Degree of unsaturationMaterials scienceRenewable Energy Sustainability and the EnvironmentTall oilDecarboxylationGeneral Chemical EngineeringThermosetting polymer02 engineering and technologyGeneral ChemistryEpoxy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesChemical engineeringFlexural strengthReagentvisual_artvisual_art.visual_art_mediumEnvironmental Chemistry0210 nano-technologyCuring (chemistry)ACS Sustainable Chemistry & Engineering
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Dynamic chemical devices: photoinduced electron transfer and its ion-triggered switching in nanomechanical butterfly-type bis(porphyrin)terpyridines.

2005

A series of butterfly-type molecular constructs has been prepared in good yield by using a double Stille coupling synthetic protocol. They are composed of a terpyridine (terpy) scaffold and two wings composed of appended porphyrins that are capable of switching from an extended W geometry to a compact U geometry upon cation coordination of the terpy unit. The porphyrin moieties exist in the constructs either as free bases or they can be sequentially metallated, thus giving rise to wings of different "colours". Stationary and time-resolved emission studies of the HZn, ZnAu and Zn2Au constructs show that the electronic properties are strongly dependent on the geometry. In the extended W confo…

DenticityMagnetic Resonance SpectroscopyPorphyrinsChemical PhenomenaPhotochemistryPyridinesMolecular ConformationElectronsPhotochemistryCrystallography X-RayLigandsCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferLigandHydrogen bondChemistry PhysicalOrganic ChemistryTemperatureGeneral ChemistryHydrogen-Ion ConcentrationPorphyrinZincSpectrometry FluorescencechemistryExcited stateSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIndicators and ReagentsSpectrophotometry UltravioletTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
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Tuning the Structure of Galacturonate Hydrogels: External Gelation by Ca, Zn, or Fe Cationic Cross-Linkers

2019

International audience; We show here how the nature of various divalent cations M2+ (Ca2+, Zn2+, or Fe2+) influences the structure and mechanical properties of ionotropic polygalacturonate (polyGal) hydrogels designed by the diffusion of cations along one direction (external gelation). All hydrogels exhibit strong gradients of polyGal and cation concentrations, which are similar for all studied cations with a constant ratio R = [M2+]/[Gal] equal to 0.25, showing that every M2+ cation interacts with four galacturonate (Gal) units all along the gels. The regions of the hydrogels formed in the early stages of the gelation process are also similar for all cations and are homogeneous, with the s…

DenticityPolymers and PlasticsDiffusionIronBioengineering02 engineering and technology010402 general chemistry01 natural sciencesDivalentBiomaterialsCations[SDV.IDA]Life Sciences [q-bio]/Food engineeringMaterials ChemistrypolyGal and cation concentrationsColloidschemistry.chemical_classificationChemistryHexuronic AcidsCationic polymerizationHydrogelsDynamic mechanical analysis021001 nanoscience & nanotechnologySmall-angle neutron scattering0104 chemical sciencesionotropic polygalacturonate (polyGal) hydrogelsCrystallographyZincCross-Linking ReagentsHomogeneousSelf-healing hydrogelsCalcium0210 nano-technology
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2.14 Selected Diastereoselective Reactions: Enolate Alkylation

2012

This chapter discusses processes in which enolates are subjected to reaction with alkylating reagents. In all the processes examined here, at least one of the two reaction components is chiral and the reaction gives rise to one or more diastereomeric compounds. In most cases, the enolate is generated through deprotonation of the corresponding carbonyl precursor with a suitable base, but in several cases, the enolate is generated differently, for example, through Michael addition of a nucleophile to a conjugated carbonyl compound. The various factors that have been found to influence the stereochemical outcome of the alkylation reaction in a measurable way are also discussed. The material ha…

DeprotonationNucleophileChemistryReagentDiastereomerMichael reactionOrganic chemistryAldol condensationConjugated systemAlkylation
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New optical paper sensor for in situ measurement of hydrogen sulphide in waters and atmospheres

2016

A novel and low-cost colorimetric sensor for the determination of hydrogen sulphide in environmental samples has been developed. This sensor is based on the immobilization of the reagent N,N-Dimethyl-p-phenylenediamine and FeCl3 in paper support, in which the H2S is adsorbed in order to give rise to the formation of methylene blue as reaction product. The sensor has been applied to determine H2S in water and air samples. Two different sampling systems for H2S caption from the air have been assayed: active and passive sampling. The analytical properties of the different systems have been obtained and compared. The analytical signals, corresponding to the methylene blue, have been obtained me…

Detection limitAccuracy and precision010401 analytical chemistryAnalytical chemistry02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesSignal0104 chemical sciencesAnalytical ChemistryAbsorbancechemistry.chemical_compoundchemistrySampling (signal processing)ReagentNaked eye0210 nano-technologyDerivatizationTalanta
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Determination of methamphetamine in urine samples with sodium 1,2-naphthoquinone-4-sulphonate

1994

Optimal conditions have been studied for the determination of methamphetamine in urine samples by an extractive-spectrophotometric method with sodium 1,2-naphthoquinone-4-sulphonate (NQS) as reagent. These conditions are: NaHCO3 pH 10, NQS 6.3 × 10−3 mol/l and heating for 5 min at 45°C. The accuracy and precision of the method were tested. The detection limits were 0.2 mg/l in the standard and 0.9 mg/l when 5 ml of urine sample were taken. The standard deviation of blank urine was evaluated from 12 different samples. The relative errors found in the determination of methamphetamine in urine were lower than 10% if the methamphetamine-amphetamine ratio was higher than 4.

Detection limitAccuracy and precisionChromatographyChemistrySodiumNQSchemistry.chemical_elementUrineMethamphetamineBiochemistryAnalytical ChemistryReagentmedicineQuantitative analysis (chemistry)medicine.drugFresenius' Journal of Analytical Chemistry
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Liquid Chromatographic Analysis of Amphetamine and Related Compounds in Urine Using Solid-Phase Extraction and 3,5-Dinitrobenzoyl Chloride for Deriva…

1997

A chromatographic method for the analysis of amphetamine and related compounds in urine using 3,5-dinitrobenzoyl chloride (3,5-DNB) as a labeling reagent is presented. This assay is based on the employment of solid-phase extraction (SPE) cartridges for sample cleanup and derivatization. Experimental conditions are optimized for the simultaneous derivatization of ephedrine, norephedrine, pseudoephedrine, beta-phenylethylamine, amphetamine, methamphetamine, and 3-phenylpropylamine. The derivatives formed are separated in a LiChrospher 1000 RP18 (125 x 4-mm i.d., 5-microns film thickness) analytical column using a water-acetonitrile gradient elution and detected at 254 nm. Derivatization in C1…

Detection limitAnalyteChromatographyAmphetaminesGeneral MedicinePseudoephedrineHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNitrobenzoatesReagentmedicineIndicators and ReagentsSolid phase extractionEphedrineDerivatizationChromatography High Pressure Liquidmedicine.drugJournal of Chromatographic Science
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Analysis of methylamine by solid-phase microextraction and HPLC after on-fibre derivatization with 9-fluorenylmethyl chloroformate

2004

Abstract A method for the determination of methylamine (MA) in aqueous matrices is reported which uses solid-phase microextraction (SPME) for enrichment and derivatization of the analyte, and high performance liquid chromatography (HPLC). The fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC) has been used for derivatization. The SPME fibres were successively immersed in the samples and in the derivatization solutions to extract MA and FMOC, respectively. After a defined time of reaction, the derivatized analyte was desorbed into the chromatographic system, and chromatographed in a LiChrosphere 100 RP18, 125 mm ×4 mm i.d., 5 μm, column under gradient elution. In order to improve the…

Detection limitAnalyteChromatographyChemistryChloroformateSolid-phase microextractionBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundReagentEnvironmental ChemistrySample preparationDerivatizationSpectroscopyAnalytica Chimica Acta
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High-performance liquid chromatographic determination of spironolactone and its major metabolite canrenone in urine using ultraviolet detection and c…

1994

A rapid and simple column liquid chromatographic method involving a column-switching system for the determination of spironolactone and its main metabolite canrenone in urine is described. Purification and concentration was performed using an Hypersil ODS-C18, 30 microns (20 x 2.1 mm I.D.) pre-column. The most polar urinary compounds were removed by washing the pre-column with water, and the analytes were subsequently switched to a LiChrospher RP C18, 5 microns (125 x 4 mm I.D.) analytical column and separated by means of an acetonitrile-water mobile-phase. Under the proposed conditions, the extraction efficiency was approximately 100% over the 0.5-10.0 micrograms/ml concentration range. Th…

Detection limitAnalyteChromatographyChemistryMetaboliteExtraction (chemistry)General ChemistryUrineSpironolactoneHigh-performance liquid chromatographychemistry.chemical_compoundCanrenonemedicineHumansIndicators and ReagentsSpectrophotometry UltravioletCanrenoneQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical applications
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Automated high-performance liquid chromatographic determination of amphetamine in biological fluids using column-switching and on-column derivatizati…

1999

A rapid and simple liquid-chromatographic method has been developed for on-line quantification of amphetamine in biological fluids. Untreated samples (20 μL) are injected directly into the chromatographic system and purified on a 20 mm×2.1 mm i.d. pre-column packed with 30 μm Hypersil C18 stationary phase. After clean-up the analyte is transferred to the analytical column (125 mm×4 mm i.d., 5 μm LiChrospher 100 RP18) for derivatization and separation using a mixture of acetonitrile and the derivatization reagent (o-phthaldialdehyde andN-acetyl-L-cysteine) as the mobile phase. The experimental conditions for on-line derivatization and resolution of the amphetamine have been optimized, and th…

Detection limitAnalyteChromatographyResolution (mass spectrometry)Organic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundchemistryReagentDerivatizationQuantitative analysis (chemistry)Chromatographia
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