Search results for "Solid"

showing 10 items of 3575 documents

Quantification of low levels of amorphous content in sucrose by hyperDSC.

2005

A method was developed for the quantification of low levels of amorphous content in sucrose with hyperDSC. The method was based on the fact that the change of specific heat at the glass transition is linearly proportional to the amorphous content. It was found out that as annealing time increased, the glass transition temperature moved to a higher temperature and the change of specific heat increased. DeltaC(p) for annealed totally amorphous sucrose was 0.761+/-0.012 Jg(-1) degrees C(-1). Synthetic mixtures with various proportions of crystalline and amorphous sucrose were prepared. The following linear regression between DeltaC(p) and amorphous content was obtained: DeltaC(p)=0.0075x - 0.0…

Detection limitSucroseSucroseMaterials scienceSpecific heatCalorimetry Differential ScanningAnnealing (metallurgy)Analytical chemistryPharmaceutical ScienceMineralogyReproducibility of ResultsAmorphous solidGrindingchemistry.chemical_compoundchemistryRegression AnalysisThermodynamicsTransition TemperatureGlass transitionCrystallizationInternational journal of pharmaceutics
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Identification of the Biotransformation Products of 2-Ethylhexyl 4-(N,N-Dimethylamino)benzoate

2010

Nowadays, 2-ethylhexyl 4-(N,N-dimethylamino)benzoate (EDP) is one of the most widely used UV filters in sunscreen cosmetics and other cosmetic products. However, undesirable processes such as percutaneous absorption and biological activity have been attributed to this compound. The in vitro metabolism of EDP was elucidated in the present work. First of all, the phase I biotransformation was studied in rat liver microsomes and two metabolites, N,N-dimethyl-p-aminobenzoic acid (DMP) and N-monomethyl-p-aminobenzoic acid (MMP), were identified by GC-MS analysis. Secondly, the phase II metabolism was investigated by means of LC-MS. The investigated reactions were acetylation and glucuronidation …

Detection limitSunscreen cosmeticsChromatographyChemistryOriginalMetaboliteOrganic ChemistryClinical BiochemistryGlucuronidation2-Ethylhexyl 4-(NN-dimethylamino)benzoateHigh-performance liquid chromatographyBiochemistryAnalytical Chemistrychemistry.chemical_compoundBiotransformationLiquid chromatography–mass spectrometryMicrosomeSolid phase extractionLiquid chromatography-mass spectrometryUV filtering
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Simple and sensitive reversed-phase liquid chromatographic assay for analysis of chlorthalidone in urine

1993

Abstract This study describes a rapid method for the determination of chlorthalidone in human urine by reversed-phase liquid chromatography and UV detection at 230 nm, after clean-up over a C8 solid-phase extraction column. Liquid chromatography was carried out on a C18-bonded phase using acetonitrile-phosphate buffer (pH=3) gradient elution. Triamterene was used as internal standard. The system has been applied to the determination of chlorthalidone in the 0.10–10.0 μg/mL concentration interval; the limit of detection was 6 ng/mL.

Detection limitTriamtereneChromatographyChemistryExtraction (chemistry)medicineMolecular MedicineChlorthalidoneSolid phase extractionReversed-phase chromatographyHigh-performance liquid chromatographyQuantitative analysis (chemistry)medicine.drug
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Comparison of different sorbents for on-line liquid-solid extraction followed by high-performance liquid chromatographic determination of nitrogen-co…

1998

Abstract LiChrolut EN [poly(styrene-divinylbenzene), PSDVB], Carbograph (graphitized carbon black, GCB), Isolute CN (cyanopropylsilica), Isolute C 2 (ethylsilica), and LiChrospher RP18 (octadecylsilica) were studied for on-line solid-phase extraction of twelve nitrogen containing pesticides from water. Determination (UV 210 nm) was performed with a Spherisorb C 8 analytical column and an acetonitrile-water gradient. The mean recoveries from 50 ml ranged from 83% for RP18 to 44% for GCB, and decreased in the following order: RP18, CN, LiChrolut EN, C 2 , and GCB. GCB showed poor recoveries due to incomplete desorption with the acetonitrile-water gradient used, and memory effects were detecte…

Detection limitVinyl CompoundsChromatographyNitrogenChemistryElutionOrganic ChemistryExtraction (chemistry)General MedicineReversed-phase chromatographySilicon DioxideBiochemistryHigh-performance liquid chromatographyBackflush accountingCarbonAnalytical ChemistryPolystyrenesIndicators and ReagentsSpectrophotometry UltravioletSample preparationSolid phase extractionPesticidesChromatography High Pressure LiquidJournal of Chromatography A
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Bio-metal-organic frameworks for molecular recognition and sorbent extraction of hydrophilic vitamins followed by their determination using HPLC-UV

2020

A bio-metal-organic framework (bio-MOF) derived from the amino acid L-serine has been prepared in bulk form and evaluated as sorbent for the molecular recognition and extraction of B-vitamins. The functional pores of bio-MOF exhibit high amounts of hydroxyl groups jointly directing other supramolecular host-guest interactions thus providing the recognition of B-vitamins in fruit juices and energy drinks. Single-crystal X-ray diffraction studies reveal the specific B-vitamin binding sites and the existence of multiple hydrogen bonds between these target molecules and the framework. It offered unique snapshots to accomplish an efficient capture of these solutes in complex aqueous matrices. Fo…

Detection limitVitaminesSorbentChromatographySurface PropertiesUltraviolet RaysElutionChemistryHydrophilic interaction chromatography010401 analytical chemistryExtraction (chemistry)Supramolecular chemistryQuímica analítica010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryBegudesMolecular recognitionVitamin B ComplexAdsorptionSolid phase extractionParticle SizeHydrophobic and Hydrophilic InteractionsMetal-Organic FrameworksMicrochimica Acta
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Online Solid-Phase Extraction LC-MS/MS: A Rapid and Valid Method for the Determination of Perfluorinated Compounds at Sub ng·L-1Level in Natural Water

2018

In this research paper, we report a method able to detect perfluorinated compound at pg·L−1 levels in superficial and underground water samples. An online solid phase extraction HPLC-MS/MS method was developed for the analysis of 12 perfluoroalkyl acids (PFASs). The method is based on injection of 5000 µL of water sample in SPE online WAX column followed by chromatography separation and mass spectrometry determination. SPE online elution was performed by water + 0.05% NH4OH and methanol + 0.05% NH4OH, while separation of target compounds was achieved within 10 min by Gemini chromatographic column operating from 1 to 12 pH range and using a mixture of water-methanol + 0.05% NH4OH. Sub ng·L−1…

Detection limitWaxChromatographyArticle SubjectElution010401 analytical chemistryChemistry (all)Perfluorinated compoundGeneral Chemistry010501 environmental sciencesMass spectrometry01 natural sciences0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999visual_artLc ms msvisual_art.visual_art_mediumSolid phase extractionQuantitative analysis (chemistry)0105 earth and related environmental sciences
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Determination of carbonyl compounds in particulate matter PM2.5 by in-tube solid-phase microextraction coupled to capillary liquid chromatography/mas…

2013

Abstract In this paper, a new procedure based on in-tube solid phase microextraction (IT-SPME)-capillary liquid chromatography hyphenated to mass spectrometry detection by using microelectrospray ionisation (CapLC–MS), has been reported. The device was proposed to quantify 12 carbonyl compounds (10 aliphatic aldehydes, an unsaturated aldehyde and a ketone) derivatized with 2,4-dinitrophenylhidrazine (DNPH) reagent in aqueous extracts of PM 2.5 . This methodology involves the on-line preconcentration of DNPH-carbonyl compounds derivatives coupled to the CapLC–MS system, efficiently providing appropriate sensitivity for the determination of the target analytes. Detection limits for the analyt…

Detection limitchemistry.chemical_classificationAnalyteAldehydesChromatographyKetoneAnalytical chemistryKetonesMass spectrometrySolid-phase microextractionAldehydeMass SpectrometryAnalytical ChemistryPhenylhydrazineschemistryLiquid chromatography–mass spectrometryLimit of DetectionReagentParticulate MatterSolid Phase MicroextractionWater Pollutants ChemicalChromatography LiquidTalanta
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Comparative study of the determination of trimethylamine in water and air by combining liquid chromatography and solid-phase microextraction with on-…

2005

This work describes a new approach for the determination of trimethylamine (TMA) in water and air by liquid chromatography (LC). The assay is based on the employment of a solid-phase microextraction (SPME) fiber for sampling and for derivatization of the analyte with the fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC). The fiber, with a Carbowax-templated resin -50mum coating, was first immersed into a solution of the reagent. Once loaded with the reagent, the fiber was immersed into the water samples or exposed to the air samples in order to extract and to derivatize the analyte. Finally, the fiber was placed into a HPLC-SPME interface to desorb and transfer the TMA-FMOC derivat…

Detection limitchemistry.chemical_compoundAnalyteChromatographychemistryReagentAnalytical chemistryTrimethylamineFiberChloroformateSolid-phase microextractionDerivatizationAnalytical ChemistryTalanta
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Spectrophotometric determination of carbaryl by on-line elution after its preconcentration onto polyurethane foam.

2000

Abstract An analytical methodology has been developed for the UV-spectrophotometric determination of carbaryl in waters after its preconcentration onto a polyether type polyurethane foam followed by on-line elution. The aforementioned strategy offers an easy way for in-field sampling and to improve the analytical sensitivity. Several chemical and flow variables (mass of sorbent, sample flow rate, sample volume and carrier flow rate) were studied to ensure the best performance of the system. Recovery studies, carried out on natural water samples spiked with known amounts of carbaryl at concentration levels between 250 and 500 μg l−1, provided recovery percentages between 94 and 105%. A detec…

Detection limitchemistry.chemical_compoundSorbentChromatographychemistryElutionCarbarylSorptionSolid phase extractionAnalytical ChemistryPolyurethaneVolumetric flow rateTalanta
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X-ray structures of five variably tert-butoxycarbonyl-substituted adenines and their liquid and solid state NMR investigations

2009

Abstract Adenine reacts selectively with di- tert -butyldicarbonate in THF in the presence of NaOH to give N 9-monoBoc-adenine 1 . The molecular structure and crystal packing of this and four other variably substituted Boc-derivatives of adenine were determined in solid state by means of X-ray diffraction and CP/MAS NMR experiments and characterized in liquid state by 1 H, 13 C, and 15 N NMR spectroscopy as well. Additionally, crystal structure of inclusion compound between N 6 -monoBoc-adenine 5 and CHCl 3 is reported. Tautomeric equilibria of mono- and disubstituted derivatives 4 and 5 in liquid state were studied by VT NMR experiments.

Deuterium NMRCarbon-13 NMR satelliteOrganic ChemistryNuclear magnetic resonance spectroscopy of nucleic acidsNuclear magnetic resonance spectroscopyCrystal structureNuclear magnetic resonance crystallographyAnalytical ChemistryInclusion compoundInorganic ChemistryCrystallographychemistry.chemical_compoundSolid-state nuclear magnetic resonancechemistrySpectroscopyJournal of Molecular Structure
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