Search results for "performance"

showing 10 items of 4457 documents

A multinjection strategy for mercury speciation.

2005

Abstract A multiinjection strategy has been developed to increase the sampling throughput of the high-performance liquid chromatography determination of inorganic-mercury, methylmercury, ethylmercury and phenylmercury. The method involves the injection of samples each 3.5 min, in spite of the fact that phenylmercury retention time corresponds to 9.04 min. In the selected conditions, the sampling frequency was 11 h −1 in front of that of 6 h −1 , obtained by conventional injection of each sample after the complete elution of Hg species. Additionally, the analytical reagents consumption was reduced drastically in almost 50%. The main characteristics of the chromatographic separation were main…

ChromatographyElutionAnalytical chemistrychemistry.chemical_elementHigh-performance liquid chromatographyAnalytical ChemistryMercury (element)Ethylmercurychemistry.chemical_compoundChromatographic separationchemistryReagentRetention timeMethylmercuryTalanta
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Comparative study of capillary electroendosmotic chromatography and electrically assisted gradient nano-liquid chromatography for the separation of p…

2000

Capillary electroendoendosmotic chromatography (CEC), being a hybrid of high-performance liquid chromatography (HPLC) and capillary electrophoresis, offers considerable changes to enhance column efficiency, speed of analysis and additional selectivity as compared to the parent methods. The analytes are driven by the electroendosmotic flow (EOF) and separated by surface-solute interactions as well as by differences in electromigration. In this paper on the separation of peptides on C18 reversed-phase and mixed-mode (sulphonic acid-n-alkyl) packings in CEC and electrically assisted reversed-phase gradient nano-LC are investigated. It is shown that mixed mode packings generate a higher EOF tha…

ChromatographyElutionChemistryOrganic ChemistryAnalytical chemistryElectrophoresis CapillaryCytochrome c GroupGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAngiotensin IIAnalytical ChemistryCapillary electrophoresisColumn chromatographyMixed-mode chromatographyElectrochromatographyPeptidesChromatography High Pressure LiquidJournal of chromatography. A
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Microporous hypercrosslinked polystyrene Styrosorb as a restricted access packing in sample clean-up for high performance liquid chromatography. Part…

1993

Styrosorb is a beaded microporous polystyrene with particle sizes between 2 and 4 μm. In spite of hypercrosslinkage the material was seen to swell in organic solvents. The native material is functionalized with Tris-groups at the outer surface of the particles. The average pore diameter was determined as 1.45±0.3 nm from size exclusion data using polystyrene and polyethylene standards in THF. The reversed phase behavior of the restricted access phase Styrosorb was investigated by injection of two test mixtures. Mixture I contained five aromatic amines, mixture II consisted of AmperozideR and four related compounds. The optimum range of mobile phase composition was assessed so that analytes …

ChromatographyElutionChemistryOrganic ChemistryClinical BiochemistrySize-exclusion chromatographyMicroporous materialPolyethyleneBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundPhase (matter)ParticlePolystyreneChromatographia
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Prediction of peak shape as a function of retention in reversed-phase liquid chromatography

2004

Optimisation of the resolution of multicomponent samples in HPLC is usually carried out by changing the elution conditions and considering the variation in retention of the analytes, to which a standard peak shape is assigned. However, the change in peak shape with the composition of the mobile phase can ruin the optimisation process, yielding unexpected overlaps in the experimental chromatograms for the predicted optimum, especially for complex mixtures. The possibility of modelling peak shape, in addition to peak position, is therefore attractive. A simple modified-Gaussian model with a parabolic variance, which is a function of conventional experimental parameters: retention time (tR), p…

ChromatographyElutionChemistryOrganic ChemistryResolution (electron density)Analytical chemistryGeneral MedicineReversed-phase chromatographyFunction (mathematics)Models TheoreticalBiochemistryHigh-performance liquid chromatographyStandard deviationAnalytical ChemistryApproximation errorPhase (matter)Chromatography LiquidJournal of Chromatography A
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BEHAVIOUR OF GRAPHITIZED CARBON BLACK IN THE EXTRACTION OF POLAR NON-IONIC NITROGEN-CONTAINING PESTICIDES. A CHECKING OF HYPOTHESES

2000

Graphitized Carbon Black (GCB) extractive cartridges are evaluated for on-line coupling with a C8 analytical column to determine eleven carbamates and one carboximide pesticide from spiked deionized water at the 1.2 μg/L level. Several experiments were carried out to ascertain whether GCB saturation, pesticide degradation on the surface, existence of by-pass channels, mobility among the bulk cartridge, or strong retention on the surface interfere with the determination of pesticides. Problems in on-line CGB elution are partially solved by modifying the acetonitrile/water gradient to contain a front of 100% acetonitrile for a few seconds. Eluting the same GCB cartridges off-line with dichlor…

ChromatographyElutionClinical BiochemistryPharmaceutical ScienceReversed-phase chromatographyCarbon blackBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPesticide degradationSample preparationSolid phase extractionDichloromethaneJournal of Liquid Chromatography & Related Technologies
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Rapid method for analysis of nicotine and nicotine-related substances in chewing gum formulations

1998

Abstract Based on environmental requirements and demands for a high throughput a rapid method for the analysis of nicotine and nicotine-related substances in chewing gum formulations was developed. The method is based on sample preparation through liquid–liquid extraction followed by reversed-phase HPLC using gradient elution. It allowed up to nine analytes to be determined within 15 min, including the sample preparation, and was considered as accurate and robust.

ChromatographyElutionOrganic ChemistryAnabasineGeneral MedicineBiochemistryHigh-performance liquid chromatographyDosage formAnalytical ChemistryNicotinechemistry.chemical_compoundchemistrymedicineSample preparationMyosmineAnatabinemedicine.drugJournal of Chromatography A
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Micellar liquid chromatography: suitable technique for screening analysis.

2002

The screening capability of micellar liquid chromatography (MLC) is discussed using the reported chromatographic data of several sets of compounds (amino acids, beta-blockers, diuretics, phenethylamines, phenols, polynuclear aromatic hydrocarbons, steroids and sulfonamides) and new results (sulfonamides and steroids). The chromatographic data are treated with an interpretive optimisation resolution procedure to obtain the best separation conditions. Usually, the pH and the concentration of surfactant (sodium dodecyl sulfate, SDS, or cetyltrimethylammonium bromide) for the optimal mobile phase were 2.5-3 and0.12 M, respectively. The nature and concentration of organic solvent depended on the…

ChromatographyElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPropanolPartition coefficientchemistry.chemical_compoundColumn chromatographychemistryPharmaceutical PreparationsMicellar liquid chromatographySodium dodecyl sulfateChromatography LiquidJournal of chromatography. A
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Solid-phase extraction of quaternary ammonium herbicides

2000

This paper highlights recent advances in the solid-phase extraction (SPE) of quaternary ammonium herbicides in water, soil, plant and biological samples. After a brief introduction summarizing the properties of quaternary ammonium herbicides and the difficulties involved in measuring them, attention is paid primarily to solid supports used for isolation and concentration, pre-treatments required for the different matrices, and eluents applied for quantitative desorption of these analytes. The determination techniques used after SPE and applications of the proposed SPE methodology are also briefly discussed.

ChromatographyEnvironmental analysisHerbicidesChemistryOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundAdsorptionDesorptionSample preparationTrace analysisAmmoniumSolid phase extractionChromatography LiquidJournal of Chromatography A
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Effects of thermal processing and storage on available lysine and furfural compounds contents of infant formulas.

2000

The Maillard reaction-related effects that thermal treatments during the manufacturing process and storage (at 20 and 37 degrees C) have on powdered adapted and follow-up milk-based infant formulas were estimated by measuring the available lysine and furfural compounds contents of raw cow milk used in manufacturing, intermediate products and formulas. A fluorimetric method was used to measure the available lysine contents, and free and total furfural compounds were determined by HPLC. Statistically significant losses in available lysine (about 20%) in the infant formulas with respect to raw milk were found. The storage period did not affect the available lysine contents of adapted formulas …

ChromatographyFood HandlingLysineLysineGeneral ChemistryRaw milkFurfuralHigh-performance liquid chromatographyCow milkchemistry.chemical_compoundMaillard reactionsymbols.namesakechemistryMethyl KetonesymbolsFuraldehydeInfant FoodFood scienceGeneral Agricultural and Biological SciencesHydroxymethylfurfuralJournal of agricultural and food chemistry
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Analysis of neuropeptide Y and its metabolites by high-performance liquid chromatography-electrospray ionization mass spectrometry and integrated sam…

2000

A novel restricted access cation exchanger with sulphonic acid groups at the internal surface was proven to be highly suitable in the sample clean up of peptides on-line coupled to HPLC-electrospray ionization (ESI)-MS. Neuropeptide Y (NPY) and several of its fragments in plasma were subjected to the sample clean-up procedure. The peptides were eluted by a step gradient from the restricted access column, applying 10 mM phosphate buffer pH 3.5 from 5 to 20% (v/v) of acetonitrile with 1 M NaCl and transferred to a Micra ODS II column (33x4.6 mm). The separation of the peptides and their fragments was performed by a linear gradient from 20 to 60% (v/v) acetonitrile in water with 0.1% formic ac…

ChromatographyFormic acidElectrospray ionizationOrganic ChemistryMolecular Sequence DataGeneral MedicineReversed-phase chromatographyMass spectrometryBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryTrifluoroacetic acidAnimalsSample preparationNeuropeptide YSolid phase extractionAmino Acid SequenceCation Exchange ResinsSulfonic AcidsChromatography High Pressure LiquidJournal of chromatography. A
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