Search results for "Enrichment factor"

showing 10 items of 23 documents

Determination of free formaldehyde in cosmetics containing formaldehyde-releasing preservatives by reversed-phase dispersive liquid-liquid microextra…

2017

Abstract An analytical method for the determination of traces of formaldehyde in cosmetic products containing formaldehyde-releasing preservatives has been developed. The method is based on reversed-phase dispersive liquid–liquid microextraction (RP-DLLME), that allows the extraction of highly polar compounds, followed by liquid chromatography–ultraviolet/visible (LC–UV/vis) determination with post-column derivatization. The variables involved in the RP-DLLME process were studied to provide the best enrichment factors. Under the selected conditions, a mixture of 500 μL of acetonitrile (disperser solvent) and 50 μL of water (extraction solvent) was rapidly injected into 5 mL of toluene sampl…

AcetonitrilesLiquid Phase Microextraction02 engineering and technologyCosmetics01 natural sciencesBiochemistryChemistry Techniques AnalyticalAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionFormaldehydeAcetonitrileDerivatizationDetection limitChromatographyElution010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Preservatives PharmaceuticalReproducibility of ResultsWaterGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesSolventchemistryReagentSolvents0210 nano-technologyEnrichment factorChromatography LiquidTolueneJournal of chromatography. A
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Environmental applications (air)

2020

Abstract The use of solid sorbent-based devices for the monitoring of contaminants in the air is a widespread trend due to its versatility, physicochemical stability, and high enrichment factor. Active and passive sampling strategies have been developed for air monitoring using different materials, such as carbon-based organic polymers and inorganic sorbents. It has been updated in the literature regarding the most recent applications of the use of solid sorbent-based samplers for the monitoring of air in different sites such as rural, urban, industrialized, and indoor areas, including workplace environments for the evaluation of occupational exposure risks.

Air monitoringSorbentWaste managementEnvironmental scienceOccupational exposureContaminationEnrichment factorPassive sampling
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Voltammetric Analysis of Platinum in Environmental Matrices

2014

This article will summarize measurement data for Pt in different environmental samples obtained by the authors using a recently developed approach by voltammetric analysis. A fast accumulation of platinum and rhodium in the environmental and biological matrices has been observed in the last few years and concern has arisen about potential environmental and health risks. Voltammetry was used for the determination of Pt and Rh in airborne particulate collected in Palermo, Italy. Possible interferences by other environmental metals have also been evaluated. All samples show concentrations of Pt and Rh above average upper crust values. The Pt and Rh concentrations in particulate samples collect…

Air pollutionchemistry.chemical_elementParticulatesmedicine.disease_causeSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni Culturalilaw.inventionRhodiumchemistrylawEnvironmental chemistryCatalytic convertermedicineEnvironmental scienceSettore CHIM/01 - Chimica AnaliticaVoltammetric Analysis Platinum EnvironmentalDifferential pulse voltammetryPlatinumEnrichment factorVoltammetry
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Polycyclic aromatic hydrocarbons and trace metal contamination of coastal sediment and biota from Togo

2011

The state of contamination of tropical environments, particularly in Africa, remains a relatively under explored subject. Here, we determined polycyclic aromatic hydrocarbon (PAH) and trace metal concentrations in coastal sediment and biota samples (fish and mussels) from Togo (West Africa). In the sediments, the ∑21 PAH concentrations ranged from4 ng g(-1) to 257 ng g(-1), averaging 92 ng g(-1). Concentration ratios of low molecular weight PAHs (2-3 rings) versus high molecular weight PAHs (≥4 rings) were always lower than 1 (ranging from 0.08 to 0.46) indicating that high molecular weight PAHs were dominant in all sediment samples, and that PAHs originated mainly from anthropogenic combus…

Aquatic OrganismsGeologic SedimentsPolycyclic aromatic hydrocarbonManagement Monitoring Policy and LawAnimalsSeawaterTrace metalPolycyclic Aromatic Hydrocarbonschemistry.chemical_classificationChemistryTerrigenous sedimentFishesPublic Health Environmental and Occupational HealthSedimentBiotaGeneral MedicineBiotaBivalviaPhosphoriteMetalsTogoEnvironmental chemistryBioaccumulationEnrichment factorWater Pollutants ChemicalEnvironmental MonitoringJournal of Environmental Monitoring
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Mass levels, crustal component and trace elements in PM10 in Palermo, Italy.

2007

Abstract Results concerning the levels and elemental compositions of daily PM 10 samples collected at four air quality monitoring sites in Palermo (Italy) are presented. The highest mean value of PM 10 concentrations (46 μg m −3 , with a peak value of 158 μg m −3 ) was recorded at the Di Blasi urban station, and the lowest at Boccadifalco station (25 μg m −3 ), considered as a sub-urban background station. Seventeen elements (Al, As, Ba, Co, Cr, Cu, Fe, Li, Mn, Mo, Ni, Pb, Sb, Sr, U, V, Zn) were measured by ICP-MS. Al and Fe showed the highest concentrations, indicating the significant contribution of soil and resuspended mineral particles to atmospheric PM 10 . Ba, Cr, Cu, Mn, Mo, Ni, Pb, …

Atmospheric ScienceChemistryTrace elementAir pollutionMineralogymedicine.disease_causePM10 trace elements urban areaAerosolAir quality monitoringEnvironmental chemistrymedicineMineral particlesPeak valueEnrichment factorRoad trafficGeneral Environmental Science
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Determination of phenoxy acid herbicides in drinking waters by HPLC and solid phase extraction

1998

Abstract An HPLC procedure for determining phenoxy acid herbicides in waters is described. A LichroSpher RP select B octadecyl-silane analytical column and spectrophotometric detection at 230 nm were used. Adequate retention was achieved with a mobile phase containing MeOH/phosphate buffer 10−2 M pH 2.5/PnOH (50/42/8, v/v). The herbicides were isolated from water samples by using a single solid phase extraction procedure with C18 solid-phase columns. An enrichment factor of 500 is achieved. The coefficients of variation of the method were generally lower than 2.7% at 0.4 μg L−1 herbicide concentration levels. Recoveries ranged between 93 and 118%. The results obtained indicate that the prop…

ChromatographyChemistryClinical BiochemistryPharmaceutical ScienceReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundDicambaSample preparationSolid phase extractionWater pollutionEnrichment factorQuantitative analysis (chemistry)
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Supported liquid membrane extraction with single hollow fiber for the analysis of fluoroquinolones from environmental surface water samples

2010

Abstract In this work, the simple analytical method for the determination of four fluoroquinolone antibiotics: ciprofloxacin, enrofloxacin, norfloxacin and danofloxacin, in environmental surface water samples is described. Sample pretreatment step was performed by the application of a technique based on supported liquid membrane extraction with the configuration of single hollow fiber (HF-SLM). The HPLC system with diode array detection was used for final analysis of studied analytes. Various parameters affecting the extraction efficiency during HF-SLM enrichment, such as type of membrane diluent, pH of donor (sample) and acceptor phases, as well as an enrichment time and salt content of sa…

DanofloxacinAnalytical chemistrySodium ChlorideBiochemistryHigh-performance liquid chromatographyDiluentSensitivity and SpecificityAnalytical ChemistryRiversmedicinehollow fiberenvironmental samplesSample preparationfluoroquinolonesChromatography High Pressure LiquidDetection limitChromatographysample preparationChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsMembranes ArtificialGeneral MedicineHydrogen-Ion ConcentrationAnti-Bacterial Agentssupported liquid membrane extractionWater treatmentHydrochloric AcidEnrichment factorWater Pollutants Chemicalmedicine.drugJournal of Chromatography A
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Development of a sensitive method for determining traces of prohibited acrylamide in cosmetic products based on dispersive liquid-liquid microextract…

2020

Abstract According to the European Regulation on cosmetic products, the presence of acrylamide in these consumer products is not allowed due to its mutagenic and potentially carcinogenic effects. Despite this ban, acrylamide might be present in those cosmetic products containing acrylamide-based polymers. However, there is no analytical method for its determination in this type of matrices. Based on this, the development of analytical methods for the determination of acrylamide in cosmetic products is required to guarantee consumer safety. In this work, an analytical method for determining traces of prohibited acrylamide in cosmetic products is presented for the first time. The method is ba…

Detection limitChromatographyChloroformAqueous solutionChemistry010401 analytical chemistryExtraction (chemistry)02 engineering and technology021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundAcrylamide0210 nano-technologyDerivatizationEnrichment factorSpectroscopyMicrochemical Journal
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Determination of N-nitrosodiethanolamine in cosmetic products by reversed-phase dispersive liquid-liquid microextraction followed by liquid chromatog…

2016

A new analytical method for the determination of N-nitrosodiethanolamine (NDELA), a very harmful compound not allowed in cosmetic products, is presented. The method is based on a new approach of dispersive liquid-liquid microextraction (DLLME) useful for extraction of highly polar compounds, called reversed-phase DLLME (RP-DLLME), followed by liquid chromatography-ultraviolet/visible (LC-UV/Vis) determination. The variables involved in the RP-DLLME process were studied to provide the best enrichment factors. Under the optimized conditions, a mixture of 750µL of acetone (disperser solvent) and 125µL of water (extraction solvent) was rapidly injected into 5mL of toluene sample solution. The e…

Detection limitChromatographyElutionLiquid Phase Microextraction010401 analytical chemistryExtraction (chemistry)02 engineering and technologyCosmetics021001 nanoscience & nanotechnology01 natural sciencesToluene0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundchemistryGriess testLimit of DetectionSolventsDiethylnitrosamine0210 nano-technologyEnrichment factorAmmonium acetateChromatography LiquidTalanta
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Determination of N -nitrosamines in cosmetic products by vortex-assisted reversed-phase dispersive liquid-liquid microextraction and liquid chromatog…

2018

A new analytical method for the simultaneous determination of trace levels of seven prohibited N-nitrosamines (N-nitrosodimethylamine, N-nitrosoethylmethylamine, N-nitrosopyrrolidine, N-nitrosodiethylamine, N-nitrosopiperidine, N-nitrosomorpholine, and N-nitrosodiethanolamine) in cosmetic products has been developed. The method is based on vortex-assisted reversed-phase dispersive liquid-liquid microextraction, which allows the extraction of highly polar compounds, followed by liquid chromatography with mass spectrometry. The variables involved in the extraction process were studied to obtain the highest enrichment factor. Under the selected conditions, 75 μL of water as extraction solvent …

Detection limitNitrosaminesMaterials scienceChromatographyMolecular StructureLiquid Phase Microextraction010401 analytical chemistryExtraction (chemistry)Mixing (process engineering)Filtration and SeparationCosmetics02 engineering and technologyRepeatability021001 nanoscience & nanotechnologyMass spectrometry01 natural sciencesMass Spectrometry0104 chemical sciencesAnalytical ChemistrySolventPhase (matter)0210 nano-technologyEnrichment factorChromatography LiquidJournal of Separation Science
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