Search results for "acetonitrile"

showing 10 items of 1007 documents

Origin and correction of the deviations in retention times at increasing flow rate with Chromolith columns.

2010

Chromoliths can be used at flow rates beyond those feasible for conventional microparticulate packed columns. Ideally, the plots of the retention time versus the inverse of delivered flow rate should exhibit y-intercept of zero. However, significant positive deviations correlating with the solute polarity were observed for several compounds chromatographed with a Chromolith column, owing to the increased system pressure. Consequently, the dead time marker exhibits a smaller deviation, making the retention factors depend on the flow rate. Chromoliths are made of a silica-based monolith encapsulated within a PEEK tube, and should suffer larger stress with pressure than stainless steel columns…

Monolithic HPLC columnAcetonitrilesPolymersAnalytical chemistryBiochemistryAnalytical ChemistryPolyethylene GlycolsStress (mechanics)PropanolaminesBenzophenonesPeekMonolithChromatography High Pressure Liquidgeographygeography.geographical_feature_categoryChromatographyChemistryOrganic ChemistryGeneral MedicineDead timeKetonesSilicon DioxideVolumetric flow rateVolume (thermodynamics)Linear ModelsBar (unit)Journal of chromatography. A
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The role of water in the photocatalytic degradation of acetonitrile and toluene in gas-solid and liquid-solid regimes

2006

Photocatalytic degradation of acetonitrile and toluene was carried out both in gas-solid and in liquid-solid regimes by using commercialTiO2samples (Merck and Degussa P25). The investigation was mainly aimed to study the influence of water present in the reaction environment on the mechanism and degradation rate of two probe molecules. In gas-solid regime, the reacting mixture consisted of toluene or acetonitrile, oxygen, nitrogen, and water vapour. The main degradation product of toluene wasCO2with small amounts of benzaldehyde. In the presence of water vapour, the activity ofTiO2Merck remained stable but greatly decreased if water was absent.TiO2Degussa P25 continuously deactivated, even …

Muconic acidADSORPTIONBENZENEInorganic chemistrylcsh:TJ807-830lcsh:Renewable energy sourcesHUMIDIFIED AIRANATASE TIO2 CATALYSTOXIDATIONCH3CNBenzaldehydechemistry.chemical_compoundGeneral Materials ScienceFORMALDEHYDEBenzenePhotodegradationAcetonitrileBenzoic acidTITANIUM-DIOXIDERenewable Energy Sustainability and the EnvironmentGeneral ChemistryVAPOR-PHASETolueneAtomic and Molecular Physics and OpticsANATASE TIO2 CATALYST; TITANIUM-DIOXIDE; HUMIDIFIED AIR; VAPOR-PHASE; OXIDATION; ADSORPTION; BENZENE; CH3CN; FORMALDEHYDE; BEHAVIORchemistryBenzyl alcoholBEHAVIORInternational Journal of Photoenergy
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CCDC 705757: Experimental Crystal Structure Determination

2010

Related Article: K.Salorinne, D.P.Weimann, C.A.Schalley, M.Nissinen|2009|Eur.J.Org.Chem.|2009|6151|doi:10.1002/ejoc.200900814

N^1^N^1^'N^1^''N^1^'''-((281420-tetraethyl-6121824-tetramethoxypentacyclo[19.3.1.1^37^.1^913^.1^1519^]octacosa-1(25)3(28)469(27)101215(26)16182123-dodecaene-4101622-tetrayl)tetrakis(oxyethane-21-diyl))tetrabenzene-12-diamine acetonitrile ethanol clathrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Adsorption and photocatalytic degradation of acetonitrile: FT-IR investigation

2003

Abstract The photocatalytic degradation of acetonitrile was carried out in liquid–solid regime in a batch reactor by using two types of commercial TiO 2 powders (Merck and Degussa P25) as photocatalysts. The concentration of acetonitrile and non-purgeable organic carbon (NPOC) were monitored. The initial rate of acetonitrile conversion was found higher on TiO 2 Merck than on TiO 2 P25. FT-IR spectroscopy was used to investigate the molecular features of the adsorption and photo-oxidation of acetonitrile on the two TiO 2 powders in a fully surface hydrated form. Acetonitrile was found adsorbed on Ti 4+ surface ions and hydroxyl groups for both types of TiO 2 . This interaction appeared fully…

NitrileFF-IR investigationProcess Chemistry and TechnologyInorganic chemistryInfrared spectroscopyCatalysisTiO2; acetonitrile; adsorption; photocatalysis; FF-IR investigationTitanium oxideCatalysisacetonitrilechemistry.chemical_compoundAdsorptionchemistryadsorptionPhotocatalysisTiO2Physical and Theoretical ChemistryFourier transform infrared spectroscopyAcetonitrilephotocatalysis
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Combining poly(dimethyldiphenylsiloxane) and nitrile phases for improving the separation and quantitation of benzalkonium chloride homologues: In-tub…

2013

The retention and separation of four homologues of benzalkonium chloride (alkyl (C12, C14, C16, C18) dimethylbenzylammonium chloride) have been studied in poly(dimethyldiphenylsiloxane) (TRB) and nitrile capillary phases, respectively. Under the optimized conditions (50% acetonitrile in processed samples, 35% of diphenyl content of the TRB, capillary length 43 cm and water:methanol 60:40 as replacing solvent), the extraction efficiency was similar for all the homologues with satisfactory reproducibility and independently of the amount and proportion of homologues. Industrial samples with high viscosity or with complex composition and washes waters have been analyzed without previous treatme…

NitrileSolid-phase microextractionMass spectrometryBiochemistryChlorideMass SpectrometryAnalytical ChemistryBenzalkonium chloridechemistry.chemical_compoundLimit of DetectionNitrilesmedicineDimethylpolysiloxanesAcetonitrileSolid Phase MicroextractionChromatographyChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineSolventLinear Modelslipids (amino acids peptides and proteins)Benzalkonium Compoundsmedicine.drugChromatography LiquidJournal of chromatography. A
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Footprint of carbonyl compounds in hand scent by in-tube solid-phase microextraction coupled to nano-liquid chromatography/diode array detection

2019

Abstract In the present work, the footprint of carbonyl compounds in hand scent was achieved by a miniaturized method consisting of sampling with cotton gauze, extraction and derivatization using 2,4-dinitrophenylhydrazine (DNPH) and preconcentration, separation and detection by in-tube solid-phase microextraction (IT-SPME) coupled to nano-liquid chromatography/Uv–vis diode array detection. The coupling IT-SPME-nanoLC-DAD was solved by using a two-valve system: the first valve for loading the sample and the second one to perform IT-SPME. To this aim, a nanoparticle-based capillary column was employed. Firstly, the transfer time from the load loop to the NP-based capillary column in the IT-S…

NonanalCosmetics010402 general chemistrySolid-phase microextraction01 natural sciencesBiochemistryChemistry Techniques AnalyticalAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionHumansOrganic ChemicalsAcetonitrileDerivatizationSolid Phase MicroextractionDetection limitAldehydesChromatographyChemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)HydrazonesWaterGeneral MedicineDodecanalDecanal0104 chemical sciencesDodecanolOdorantsChromatography LiquidJournal of Chromatography A
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Analysis of a solute polarity parameter in reversed-phase liquid chromatography on a linear solvation relationship basis

2004

Abstract A study was made to correlate an overall solute polarity descriptor ( p ) with several molecular parameters: excess molar refraction ( E ), dipolarity/polarizability ( S ), effective hydrogen-bond acidity ( A ) and basicity ( B ), and McGowan volume ( V ), through the linear solvation model ( p = c + eE + sS + aA + bB + vV ). The achieved values of p were introduced in a retention model developed previously for reversed-phase liquid chromatography (RPLC), which describes the retention according to the polarity contributions of solute, mobile phase and stationary phase. The retention behaviour (log  k ) of a solute in a given chromatographic system (i.e. column/organic solvent) is a…

OctanolElutionPolarity (physics)SolvationAnalytical chemistryReversed-phase chromatographyBiochemistryAnalytical ChemistryPartition coefficientchemistry.chemical_compoundchemistryPhase (matter)Environmental ChemistryAcetonitrileSpectroscopyAnalytica Chimica Acta
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Micellar versus hydro-organic mobile phases for retention-hydrophobicity relationship studies with ionizable diuretics and an anionic surfactant

2004

Abstract Logarithm of retention factors (log  k ) of a group of 14 ionizable diuretics were correlated with the molecular (log  P o/w ) and apparent (log  P app ) octanol–water partition coefficients. The compounds were chromatographed using aqueous–organic (reversed-phase liquid chromatography, RPLC) and micellar–organic mobile phases (micellar liquid chromatography, MLC) with the anionic surfactant sodium dodecyl sulfate (SDS), in the pH range 3–7, and a conventional octadecylsilane column. Acetonitrile was used as the organic modifier in both modes. The quality of the correlations obtained for log  P app at varying ionization degree confirms that this correction is required in the aqueou…

OctanolsChromatographyStatic ElectricityOrganic ChemistryAnalytical chemistryWaterGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPartition coefficientHydrophobic effectSurface-Active Agentschemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographySpectrophotometry UltravioletSodium dodecyl sulfateDiureticsAcetonitrileChromatography High Pressure LiquidMicellesJournal of Chromatography A
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Organometallic nucleophiles.A mechanistic study of halide displacement at saturated carbon by 2- and 4-pyridyl complexes of palladium (II) and platin…

1996

Abstract The reactions of the 2- and 4-pyridyl complexes [MX(C 5 H 4 N C n )(dppe)] and trans -[MX(C 5 H 4 N C n )(PPh 3 ) 2 ] (M  Pd, Pt; X  Cl, Br; n = 2, 4)- involving halide displacement from the organic halides XCH 2 R (X  Cl, Br; R  CN, Ph, CH  CH 2 ) by the pyridyl nitrogen have been studied kinetically by conductivity in acetone or acetonitrile at 25°C. The kinetic data fit the second-order rate law rate k 2 [XCH 2 R][complex], in agreement with an S N 2 process at saturated carbon. The higher rates are displayed by the 2-pyridylplatinum derivatives with X  Br in both the metal complex and the organic halide. The higher nucleophilic power of the 2-pyridyl complexes compare…

Organic ChemistryInorganic chemistrySubstituentchemistry.chemical_elementHalideBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNucleophilechemistryPyridineMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryAcetonitrileCoordination geometryPalladium
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Substituted methyl 5β-cholan-24-oates. I—17O NMR spectral characterization

1994

Methyl esters of four common bile acids, 3α-hydroxy-5-β-cholan-24-oic (lithocholic) acid, 3α, 7α-dihydroxy-5β-cholan-24-oic (chenodeoxycholic) acid, 3α,12α-dihydroxy-5β-cholan-24-oic (deoxycholic) acid and 3α,7α,12α-trihydroxy-5β-cholan-24-oic (cholic) acid, and 14 acetylated, trifluoroacetylated, mesylated and oxo derivatives of methyl 5β-cholan-24-oates were prepared and their 17O NMR spectra recorded. In spite of their relatively high molecular masses and the rigid molecular structure of the steroid skeleton, most of the oxygens included in these structures gave well resolved 17O NMR resonance lines at natural abundance in 0.25–0.5 M acetonitrile solutions at 75°C. In agreement with the …

Oxygen-17NMR spectra databasechemistry.chemical_compoundchemistryStereochemistryAlkane stereochemistryRelaxation (NMR)SubstituentMoleculeGeneral Materials ScienceGeneral ChemistryResonance (chemistry)AcetonitrileMagnetic Resonance in Chemistry
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