Search results for "Onium"

showing 10 items of 2091 documents

Novel water-swellable beads based on an acryloylated polyaspartamide

2001

Spherical polymeric microparticles have been prepared by a reverse-phase suspension polymerization technique. The starting polymer was α,β-poly (N-2-hydroxyethyl)-dl-aspartamide (PHEA) partially functionalised with glycidylmethacrylate (GMA) in order to introduce reactive vinyl groups in the side chain. The PHEA–GMA copolymer obtained (PHG) was cross-linked in a mixture of water/hexane–carbon tetrachloride in the presence of sorbitan trioleate (Span 85) as surfactant and ammonium persulfate/N,N,N′,N′-tetramethylethylenediamine as initiator system. The reaction was also carried out in the presence of N,N′-dimethylacrylamide as comonomer or N,N′-ethylenebisacrylamide as a cross-linking agent.…

Aqueous solutionPolymers and PlasticsComonomerchemistry.chemical_compoundColloid and Surface ChemistryDifferential scanning calorimetrychemistryChemical engineeringPolymer chemistryMaterials ChemistrymedicineCopolymerSide chainAmmonium persulfateSuspension polymerizationPhysical and Theoretical ChemistrySwellingmedicine.symptomColloid & Polymer Science
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Catalytic reduction of nitrates and nitrites in water solution on pumice-supported Pd–Cu catalysts

2000

Abstract Two series of pumice-supported palladium and palladium–copper catalysts, prepared by impregnation with different palladium and copper precursors, were tested for the hydrogenation of aqueous nitrate and nitrite solutions. Measurements were performed in a stirred tank reactor, operating in batch conditions, in buffered water solution at atmospheric pressure and at 293 K. The activities of the catalysts were calculated in terms of nitrate and/or nitrite removal. With the monometallic Pd/pumice, the reduction of nitrite is highly selective; only 0.2% of the initial nitrite content is converted to ammonium ions. The activity in terms of turn over frequency (TOF) is higher as compared t…

Aqueous solutionProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementSelective catalytic reductionCopperCatalysisCatalysischemistry.chemical_compoundchemistryNitrateAmmoniumNitriteGeneral Environmental SciencePalladiumApplied Catalysis B: Environmental
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Dependence of the mobility of tracer ions in aqueous perchlorate solutions on the hydrogen ion concentration

2003

The dependence of the absolute individual ion mobility (AIIM) of the carrier-free radioactive ions [137Cs]Cs+, [201Tl]Tl+ and [57Co]Co2+ on the hydrogen ion concentration in aqueous perchlorate electrolyte mixtures was studied by means of the electromigration technique. The AIIM of the radioactive ions was found to decrease as the hydrogen ion concentration of the electrolyte mixture increases. Above pH > 4 there is a fairly good agreement between experimental and calculated values. Below pH 4 the experimentally observed decrease of the AIIM is not explained by the extended Debye–Huckel–Onsager limiting law. The effect can possibly be explained by a change of the dynamical properties of ele…

Aqueous solutionProtonHydroniumInorganic chemistryAnalytical chemistryGeneral Physics and AstronomyElectrolyteIonPerchloratechemistry.chemical_compoundReaction rate constantchemistryMoleculePhysical and Theoretical ChemistryPhys. Chem. Chem. Phys.
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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Influence of chloride anions on the electrodeposition and electroactivity of the polymer matrix in polypyrrole, poly( N -methylpyrrole) and polypyrro…

2004

We report electrochemical studies on the influence of a small concentration of chloride ions on the electroactivity of the polymer matrix of polypyrrole (PPy), poly(N-methylpyrrole) [p(N-MePy)] and a poly(titanocene-propyl-pyrrole) derivative, p(Tc3Py) [Tc(CH2)3NC4H4; Tc=CpCp′TiCl2; Cp=C5H5; Cp′=C5H4] in acetonitrile (AN), tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). The polymer films were obtained on Pt disc electrodes from AN solutions of the monomers containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6) as the supporting electrolyte and then transferred to the corresponding monomer-free solution. Studies in Cl−-containing solutions have shown that the p(Tc3Py) matrix…

Aqueous solutionSupporting electrolyteInorganic chemistryCondensed Matter PhysicsElectrochemistryPolypyrroleChloridechemistry.chemical_compoundMonomerchemistryTetrabutylammonium hexafluorophosphatePolymer chemistryElectrochemistrymedicineGeneral Materials ScienceElectrical and Electronic EngineeringAcetonitrilemedicine.drugJournal of Solid State Electrochemistry
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A facile microsynthesis of 14C-labelled picene

1984

Microscale Wittig olefination of commercially available [7-14C]-benzal dehyde of high specific radioactivity with aryl bromomethyl phosphonium salt and subsequent oxidative photocyclisation affords pure 14C-labelled picene in efficient yield.

ArylOrganic ChemistryPhosphonium saltBiochemistryAnalytical Chemistrychemistry.chemical_compoundPicenechemistryYield (chemistry)Drug DiscoveryWittig reactionOrganic chemistryRadiology Nuclear Medicine and imagingSpectroscopyMicroscale chemistryJournal of Labelled Compounds and Radiopharmaceuticals
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2017

Abstract. Concurrent in situ analyses of interstitial aerosol and cloud droplet residues have been conducted at the Schmücke mountain site during the Hill Cap Cloud Thuringia campaign in central Germany in September and October 2010. Cloud droplets were sampled from warm clouds (temperatures between −3 and +16 °C) by a counterflow virtual impactor and the submicron-sized residues were analyzed by a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS), while the interstitial aerosol composition was measured by an high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). During cloud-free periods, the submicron out-of-cloud aerosol was analyzed using both instruments, all…

Atmospheric Science010504 meteorology & atmospheric sciences010501 environmental sciencescomplex mixtures01 natural sciencesAerosolAmmoniachemistry.chemical_compoundchemistryNitrateNitric acidEnvironmental chemistryAmmoniumsense organsSulfateScavengingMass fraction0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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Study on ambient concentrations of PM10, PM10-2.5, PM2.5 and gaseous pollutants. Trace elements and chemical speciation of atmospheric particulates

2010

Abstract This study provides the first comprehensive report on mass concentrations of particulate matter of various sizes, inorganic and organic gas concentrations monitored at three sampling sites in the city of Palermo (Sicily, Italy). It also provides information on the water-soluble species and trace elements. A total of 2054 PM10 (1333) and PM2.5 (721) daily measurements were collected from November 2006 to February 2008. The highest mass concentrations were observed at the urban stations, average values being about two times higher than those at the suburban (control) site. Time variations in PM10 and also PM10–2.5 were observed at the urban stations, the highest concentrations being …

Atmospheric ScienceAmmonium nitrateair pollution PM10 and PM2.5 secondary airborne particulate BTX trace elementsTrace elementAir pollutionParticulatesmedicine.disease_causeAerosolSettore GEO/08 - Geochimica E Vulcanologiachemistry.chemical_compoundNitratechemistryEnvironmental chemistrymedicineNitrogen dioxideSulfateGeneral Environmental Science
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State of mixing, shape factor, number size distribution, and hygroscopic growth of the Saharan anthropogenic and mineral dust aerosol at Tinfou, Moro…

2009

The Saharan Mineral Dust Experiment (SAMUM) was conducted in May and June 2006 in Tinfou, Morocco. A H-TDMA system and a H-DMA-APS system were used to obtain hygroscopic properties of mineral dust particles at 85% RH. Dynamic shape factors of 1.11, 1.19 and 1.25 were determined for the volume equivalent diameters 720, 840 and 960 nm, respectively. During a dust event, the hydrophobic number fraction of 250 and 350 nm particles increased significantly from 30 and 65% to 53 and 75%, respectively, indicating that mineral dust particles can be as small as 200 nm in diameter. Log-normal functions for mineral dust number size distributions were obtained from total particle number size distributio…

Atmospheric ScienceAmmonium sulfateMaterials science010504 meteorology & atmospheric sciencesParticle numberaerosolhygroscopicityAtmosphärische SpurenstoffeMineralogyFraction (chemistry)010501 environmental sciencesMineral dustcomplex mixtures01 natural sciencesstate of mixingAerosolSAMUMchemistry.chemical_compoundchemistryParticle-size distributionAeolian processesShape factor0105 earth and related environmental sciencesTellus B: Chemical and Physical Meteorology
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2008

Abstract. Sulfur isotope analysis of atmospheric aerosols is a well established tool for identifying sources of sulfur in the atmosphere, estimating emission factors, and tracing the spread of sulfur from anthropogenic sources through ecosystems. Conventional gas mass spectrometry averages the isotopic compositions of several different types of sulfur aerosol particles, and therefore masks the individual isotopic signatures. In contrast, the new single particle technique presented here determines the isotopic signature of the individual particles. Primary aerosol particles retain the original isotopic signature of their source. The isotopic composition of secondary sulfates depends on the i…

Atmospheric ScienceIsotopic signaturechemistry.chemical_compoundAmmonium sulfateIsotope fractionationchemistryEnvironmental chemistryKinetic fractionationchemistry.chemical_elementSulfateSulfurEquilibrium fractionationIsotope analysisAtmospheric Chemistry and Physics
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