Search results for "Chemical engineering"

showing 10 items of 5892 documents

Synthesis, crystal structure and magnetic properties of the helical oxalate-bridged copper(II) chain {[(CH3)4N]2[Cu(C2O4)2] · H2O}n

2012

Abstract The preparation, crystal structure and magnetic properties of a new oxalate-containing copper(II) chain of formula {[(CH3)4N]2[Cu(C2O4)2] · H2O}n (1) [(CH3)4N+ = tetramethylammonium cation] are reported. The structure of 1 consists of anionic oxalate-bridged copper(II) chains, tetramethylammoniun cations and crystallization water molecules. Each copper(II) ion in 1 is surrounded by three oxalate ligands, one being bidentate and the other two exhibiting bis-bidenate coordination modes. Although all the tris-chelated copper(II) units from a given chain exhibit the same helicity, adjacent chains have opposite helicities and then an achiral structure results. Variable-temperature magne…

DenticityChemistryGeneral Chemical Engineeringchemistry.chemical_elementGeneral ChemistryCrystal structureCopperMagnetic susceptibilityOxalatelaw.inventionCrystallographychemistry.chemical_compoundFerromagnetismlawMoleculeCrystallizationComptes Rendus Chimie
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Square wave voltammetric determination of the redox state of a reversibly oxidized/reduced depolarizer in solution and in solid state

2012

Abstract Square wave voltammetric measurements allows for determining the composition of system containing a reversibly reducible/oxidable electroactive species in two oxidation states. The method is based on recording the ratio of reverse to forward peak currents. That ratio can be correlated with the molar fraction of the oxidized (or reduced) form of the depolarizer. The method was compared with cyclic voltammetric methods suggested in literature and it was tested using Fe ( CN ) 6 3 - / Fe ( CN ) 6 4 - in solution phase. Application to solid state systems is illustrated by the dehydroindigo/indigo couple in synthetic Maya Blue-type specimens prepared from indigo plus different clays whe…

DepolarizerChemistryGeneral Chemical EngineeringInorganic chemistrySolid-stateAnalytical chemistrySquare waveMole fractionSolution phaseRedoxIndigoAnalytical ChemistryOxidation stateElectrochemistryJournal of Electroanalytical Chemistry
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Desalination of oilfield produced waters via reverse electrodialysis: A techno-economical assessment

2023

Produced waters (PWs) are oilfield waste streams rich in minerals and hydrocarbons whose production rate is largely increased in last decades following the corresponding increase of energy demand. The high salinity level of PWs inhibits the adoption of cheap biological treatments. Also, desalination techniques based on osmotic membranes would require severe pre-treatments. As an alternative, Reverse ElectroDialysis (RED) and Assisted Reverse ElectroDialysis (ARED) are here proposed for the first time to reduce the salinity level of PWs. RED may also guarantee an operation cost reduction thanks to its energy generation. An ad-hoc model for RED and ARED is here developed in order to deal suit…

DesalinationMechanical EngineeringGeneral Chemical EngineeringReverse electrodialysiGeneral Materials ScienceGeneral ChemistryWastewaterAssisted reverse electrodialysiProduced waterWater Science and TechnologyTechno-economic analysis
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Comparison and improvement of the existing methods for the determination of aflatoxins in human serum by LC-MS/MS

2010

Aflatoxins are toxic metabolites of some Aspergillus flavus, A. parasiticus and A. nomius strains that occur in many foods and feeds. Aflatoxin B1 is the most abundant and toxic member of the family, and it is also the most potent hepatocarcinogen known. In order to estimate the potential human health risk of aflatoxin B1, it is useful to measure its blood concentration. In this work a rapid liquid chromatography coupled to mass spectrometry (LC-MS/MS) method for the simultaneous determination of aflatoxins B1, B2, G1 and G2 and its metabolites, aflatoxins M1 and M2 in human serum, is proposed. Small serum volumes have been used and the extracts have been obtained without any clean-up proce…

Detection limitAflatoxinChromatographybiologyGeneral Chemical EngineeringGeneral Engineeringfood and beveragesAspergillus flavusContaminationbiology.organism_classificationMass spectrometryAnalytical Chemistrychemistry.chemical_compoundBlood serumchemistryLc ms msheterocyclic compoundsMycotoxinAnalytical Methods
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Determination of tea tree oil terpenes by headspace gas chromatography mass spectrometry

2016

An alternative procedure was developed for determining quality control of terpenes in tea tree oil commercial samples. The method is based on static headspace gas chromatography mass spectrometry measurements. Absolute limits of detection ranged from 1 ng for p-cymene to 71 ng for terpinen-4-ol. The accuracy of the developed methodology was evaluated by comparing the obtained eucalyptol and terpinen-4-ol concentrations with those provided for a certified sample and by comparing the developed procedure with literature tea tree oil analysis methodology. In the same way, spiked commercial samples provided recovery values ranging between 94% and 100% for all the target analytes with relative st…

Detection limitAnalyteChromatography010405 organic chemistryChemistryGeneral Chemical Engineering010401 analytical chemistryRelative standard deviationGeneral EngineeringTea tree oilMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistryTerpenechemistry.chemical_compoundEucalyptolmedicineGas chromatographymedicine.drugAnalytical Methods
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Determination of 3-(4′-methylbenzylidene)camphor and its metabolite 3-(4′-carboxybenzylidene)camphor in human semen by solid-phase extraction and liq…

2015

An analytical method for the determination of the controversial UV filter 3-(4′-methylbenzylidene)camphor (MBC) and its metabolite 3-(4′-carboxybenzylidene)camphor (CBC) in human semen is presented. The method is based on the simultaneous hydrolysis of phase II conjugates and protein precipitation, followed by solid-phase extraction (SPE) and liquid chromatography tandem mass spectrometry (LC-MS/MS) detection. The proposed method was validated by analyzing spiked analyte-free human semen samples. Matrix-matched calibration using an analyte-free semen pool was employed. Satisfactory recoveries (92–114%) were obtained using this calibration methodology, thus showing the accuracy of the propos…

Detection limitAnalyteChromatographyChemistryGeneral Chemical EngineeringMetaboliteGeneral EngineeringMass spectrometryAnalytical Chemistrychemistry.chemical_compoundCamphorLiquid chromatography–mass spectrometryProtein precipitationSolid phase extractionAnalytical Methods
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A solid-phase extraction liquid chromatography-tandem mass spectrometry method for the percutaneous absorption assessment of 3-(4′-methylbenzylidene)…

2013

The UV filter 3-(4′-methylbenzylidene)camphor (MBC) is a common ingredient in sunscreen cosmetic products. However, different in vitro and in vivo studies suggest that MBC can cause endocrine disrupting effects. This report focuses on the development of an analytical method based on solid-phase extraction (SPE) prior to liquid chromatography tandem mass spectrometry (LC-MS/MS) for the determination of MBC and its main phase I metabolite, named 3-(4′-carboxybenzylidene)camphor (CBC), in urine from users of sunscreen cosmetic products containing MBC. The formation of phase II metabolites (i.e., glucuronide and sulphate conjugates) was also considered by carrying out an enzymatic hydrolysis of…

Detection limitAnalyteChromatographyGeneral Chemical EngineeringMetaboliteGeneral EngineeringAnalytical ChemistryCamphorchemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryStandard additionSolid phase extractionGlucuronideAnal. Methods
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Development of a gas chromatography-mass spectrometry method for the determination of ultraviolet filters in beach sand samples

2014

An analytical method for the determination of eight fat-soluble ultraviolet (UV) filters in beach sand samples is presented for the first time. The method is based on a leaching process of the target compounds from sand samples using vortex mixer agitation and further centrifugation, followed by dispersive liquid–liquid microextraction (DLLME) of the supernatant and gas chromatography-mass spectrometry (GC-MS) analysis of the DLLME extract. The variables involved in the leaching and in the DLLME processes were studied to provide the best enrichment factors. In the first case, the leaching solvent type and volume, and the vortex mixer agitation time were studied. In the case of the DLLME, th…

Detection limitAqueous solutionChromatographyChemistryGeneral Chemical EngineeringGeneral EngineeringAnalytical chemistryVortex mixerDisperserRepeatabilityMass spectrometryAnalytical ChemistryLeaching (metallurgy)Gas chromatography–mass spectrometryAnal. Methods
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Immunochromatographic Assay for Quantitation of Milk Progesterone.

1996

We describe a rapid immunochromatographic method for the quantitation of progesterone in bovine milk. The method is based on a 'competitive' assay format using the monoclonal antibody to progesterone and a progesterone-protein conjugate labelled with colloidal gold particles. The monoclonal antibody to progesterone is immobilized as a narrow detection zone on a porous membrane. The sample is mixed with colloidal gold particles coated with progesterone-protein conjugate, and the mixture is allowed to migrate past the detection zone. Migration is facilitated by capillary forces. The amount of labelled progesterone-protein conjugate bound to the detection zone, as detected by photometric scann…

Detection limitBovine milkChromatographymedicine.drug_classCapillary actionChemistryGeneral Chemical EngineeringAntibodies MonoclonalCross ReactionsMonoclonal antibodySensitivity and SpecificityChromatography AffinityMilkColloidal goldPorous membranemedicineAnimalsCattleChromatography Thin LayerProgesteroneConjugateActa Chemica Scandinavica
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Preliminary Results on the Use of Leather Chrome Shavings for Air Passive Sampling

2012

A new passive sampler based on low-density polyethylene (LDPE) layflat tube filled with chrome shavings from tannery waste residues was evaluated to determine volatile organic compounds (VOCs) in indoor and outdoor areas. VOCs were directly determined by head space-gas chromatography-mass spectrometry (HS-GC-MS) without any pretreatment of the sampler and avoiding the use of solvents. Limit of detection values ranging from 20 to 75 ng sampler−1and good repeatability values were obtained for VOCs under study with relative standard deviation values from 2.8 to 9.6% except for carbon disulfide for which it was 22.5%. The effect of the amount of chrome shavings per sampler was studied and resul…

Detection limitCarbon disulfideMaterials sciencelcsh:QD71-142Article SubjectGeneral Chemical EngineeringRelative standard deviationlcsh:Analytical chemistryRepeatabilityPolyethylenePulp and paper industrycomplex mixturesComputer Science ApplicationsAnalytical ChemistryLow-density polyethylenechemistry.chemical_compoundAdsorptionchemistryInstrumentationPassive samplingResearch ArticleJournal of Analytical Methods in Chemistry
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