Search results for "solution"

showing 10 items of 5638 documents

Dispersive liquid–liquid microextraction followed by gas chromatography–mass spectrometry for the determination of nitro musks in surface water and w…

2011

A new, simple, fast and high sensitive analytical method based on dispersive liquid-liquid microextraction (DLLME) followed by gas chromatography-mass spectrometry (GC-MS) for the simultaneous determination of nitro musks in surface water and wastewater samples is presented. Different parameters, such as the nature and volume of both the extraction and disperser solvents and the ionic strength and pH of the aqueous donor phase, were optimized. Under the selected conditions (injection of a mixture of 1 mL of acetone as disperser solvent and 50 μL of chloroform as extraction solvent, no salt addition and no pH adjustment) the figures of merit of the proposed DLLME-GC-MS method were evaluated.…

SolventDetection limitChromatographyAqueous solutionWastewaterChemistryExtraction (chemistry)Analytical chemistryWater treatmentGas chromatography–mass spectrometryMass spectrometryAnalytical ChemistryTalanta
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UCST-type behavior of poly[oligo(ethylene glycol) methyl ether methacrylate] (POEGMA) in aliphatic alcohols: solvent, co-solvent, molecular weight, a…

2011

Poly[oligo(ethylene glycol) methyl ether methacrylate] (POEGMA) is shown to possess insoluble–soluble transitions (UCST-type phase behavior) in a large variety of aliphatic alcohols. Samples of different molecular weights ranging from 5 kg mol−1 to 23 kg mol−1 prepared by the RAFT process and featuring different end groups at each end were analyzed by cloud point measurements. Transitions occurred sharply and were fully reversible. The UCST was found to increase with an increasing molecular weight. Hydrophobic (alkyl chain) end groups were found to lower the critical temperature in isopropanol, while rigid aromatic end groups raised the transition temperature. In ternary mixtures of isoprop…

SolventEnd-groupchemistry.chemical_compoundCloud pointChloroformchemistryUpper critical solution temperaturePolymer chemistryDodecanolEtherGeneral ChemistryCondensed Matter PhysicsEthylene glycolSoft Matter
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Intramolecular proton transfer of serine in aqueous solution. Mechanism and energetics

2000

Serine amino acid in aqueous solution is theoretically studied at the B3PW91/6-31+G** level using a dielectric continuum solvent model. Neutral and zwitterionic structures in the gas phase and in solution are described and the proton-transfer mechanism is discussed. A neutral conformation in which the carboxyl hydrogen atom is already oriented toward the amino group seems to be the absolute energy minimum in the gas phase and the most stable neutral form in solution. The absolute energy minimum in solution is a zwitterionic form. The energy barrier for proton transfer is predicted to be very small, in particular when zero-point-energy contributions are added. Our calculations allow the dyna…

SolventSerineQuantitative Biology::BiomoleculesAqueous solutionChemistryComputational chemistryIntramolecular forceIonizationNon-equilibrium thermodynamicsHydrogen atomDielectricPhysical and Theoretical ChemistryTheoretical Chemistry Accounts: Theory, Computation, and Modeling (Theoretica Chimica Acta)
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1983

Solutions of poly (decyl methacrylate) in isooctane (2,2, 4-trimethylpentane) show lower critical solution temperatures (LCST) that lie well below the thermal degradation of the polymer. The corresponding exothermal theta-temperature (from the Shultz-Flory plot) amounts to 210°C. The increase in solvent quality by pressure turns out to be very pronounced (d Tc/dp ≈ +1 K/bar). With solutions of the polymer in motor oils, high temperature demixing is unlikely to occur below their boiling point. The theoretical evaluation of published experimental data for 11 different systems exhibiting LCSTs demonstrates the following: Under the equilibrium vapour pressure of the solution high temperature de…

Solventchemistry.chemical_classificationBoiling pointChemistryVapor pressurePolymer chemistryMixing (process engineering)ThermodynamicsOrganic chemistryPolymerMethacrylateLower critical solution temperatureBar (unit)Die Makromolekulare Chemie
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Phosphatidylcholine-Gramicidin a Interaction Study in Non-Aqueous Solvent with a new HPLC-SEC Column

1985

Abstract A new HPLC-SEC column, Ultrastyragel 500 A, has been assayed in order to check the separation between gramicidin A and phosphatidylcholine in tetrahydrofuran. The good resolution of both compounds has allowed the quantitation of lipid-polypeptide interaction in terms of the binding ratio parameter, BR. A BR value of 3.6 moles of phosphatidylcholine per mole of gramicidin A has been obtained for a 0.1 % (w/v) phosphatidylcholine solution as eluent. The suitability of this support for studies on lipid-polypeptide interactions in non-aqueous solvents is demonstrated.

Solventchemistry.chemical_compoundAqueous solutionChromatographyColumn chromatographyResolution (mass spectrometry)chemistryPhosphatidylcholineMolecular Medicinelipids (amino acids peptides and proteins)Biological membraneHigh-performance liquid chromatographyTetrahydrofuranJournal of Liquid Chromatography
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On the ionizing properties of supercritical carbon dioxide: uncatalyzed electrophilic bromination of aromatics

2014

Supercritical carbon dioxide (scCO2), a solvent with a zero dipole moment, low dielectric constant, and no hydrogen bonding behavior, is a suitable medium to perform the uncatalyzed electrophilic bromination of weakly activated aromatics with no interference of radical pathways. The ability of scCO2 to promote these reactions matches those of strongly ionizing solvents such as aqueous acetic and trifluoroacetic acids. Conversely, carbon tetrachloride, with similar polarity parameters to scCO2, leads exclusively to side chain functionalization. The strong quadrupole moment, and the acidic, but non basic, Lewis character of carbon dioxide, are proposed as key factors for the singular performa…

Solventchemistry.chemical_compoundAqueous solutionSupercritical carbon dioxidechemistryHydrogen bondGeneral Chemical EngineeringCarbon dioxideElectrophileHalogenationIonic bondingGeneral ChemistryPhotochemistryRSC Adv.
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Zur polymerisation und copolymerisation des natriumvinylsulfonats

1959

Natriumvinylsulfonat (VS-Na) zeigt in konzentrierten wasrigen Losungen eine ausgepragte Polymerisationsneigung. Die Polymerisationsgeschwindigkeit und der erreichte Umsatz hangen stark von der Aciditat der Losungen ab. Es wurde gefunden, das mit der Polymerisationsdauer und mit wachsendem Umsatz auch die Molekulargewichte der Polymerisate ansteigen. Wasserunlosliche oder nur begrenzt losliche ungesattigte Verbindungen wie Styrol, Vinylacetat und andere konnen in Dimethylsulfoxyd in homogener Losung mit VS-Na copolymerisiert werden. Sodiumvinylsulphonate (VS-Na) shows a strong tendency for polymerization in concentrated aqueous solutions. The rate of polymerization and the conversion depend …

Solventchemistry.chemical_compoundMonomerAqueous solutionPolymerizationChemistryHomogeneousPolymer chemistryStyreneDie Makromolekulare Chemie
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Design, characterization and evaluation of hydroxyethylcellulose based novel regenerable supersorbent for heavy metal ions uptake and competitive ads…

2017

Abstract Hydroxyethylcellulose succinate-Na (HEC-Suc-Na) was designed and evaluated for removal of some heavy metal ions from aqueous solution. Pristine sorbent HEC-Suc-Na was thoroughly characterized by FTIR and solid-state CP/MAS 13C NMR spectroscopy, SEM-EDS and zero point charge analyses. Langmuir isotherm, pseudo second order kinetic and ion exchange models provided best fit to the experimental data of sorption of metal ions. Maximum sorption capacities of supersorbent HEC-Suc-Na for sorption of heavy metal ions from aqueous solution as calculated by Langmuir isotherm model were found to be 1000, 909.09, 666.6, 588 and 500 mg g−1 for Pb(II), Cr(VI), Co(II), Cu(II) and Ni(II), respectiv…

SorbentMetal ions in aqueous solutionInorganic chemistry02 engineering and technology010501 environmental sciences01 natural sciencesBiochemistryWater Purificationsymbols.namesakeStructural BiologyMetals HeavyGalvanic cellFourier transform infrared spectroscopyCelluloseMolecular Biology0105 earth and related environmental sciencesAqueous solutionIon exchangeChemistryTemperatureLangmuir adsorption modelSorptionGeneral MedicineHydrogen-Ion Concentration021001 nanoscience & nanotechnologyKineticsDrug DesignsymbolsAdsorption0210 nano-technologyWater Pollutants ChemicalInternational Journal of Biological Macromolecules
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Changes in fluid geochemistry and physico-chemical conditions of geothermal systems caused by magmatic input: The recent abrupt outgassing off the is…

2005

Abstract Hydrothermal systems and related vents can exhibit dramatic changes in their physico-chemical conditions over time as a response to varying activity in the feeding magmatic systems. Massive steam condensation and gas scrubbing processes of thermal fluids during their ascent and cooling cause further compositional changes that mask information regarding the conditions evolving at depth in the hydrothermal system. Here we propose a new stability diagram based on the CO2-CH4-CO-H2 concentrations in vapor, which aims at calculating the temperatures and pressures in hydrothermal reservoirs. To filter gas scrubbing effects, we have also developed a model for selective dissolution of CO2-…

Southern EuropeEastern HemisphereWorldPanareaGeochemistryHydrothermal circulationEuropeOutgassingItalyGeochemistry and PetrologyMagmaMessina [Sicily]EurasiaSeawaterSicilyVolatilesGeothermal gradientDissolutionGeologyLipari IslandThermal fluidsGeochimica et Cosmochimica Acta
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Filter multiplexing by use of spatial Code Division Multiple Access approach.

2003

The increasing popularity of optical communication has also brought a demand for a broader bandwidth. The trend, naturally, was to implement methods from traditional electronic communication. One of the most effective traditional methods is Code Division Multiple Access. In this research, we suggest the use of this approach for spatial coding applied to images. The approach is to multiplex several filters into one plane while keeping their mutual orthogonality. It is shown that if the filters are limited by their bandwidth, the output of all the filters can be sampled in the original image resolution and fully recovered through an all-optical setup. The theoretical analysis of such a setup …

Spatial filterbusiness.industryComputer scienceCode division multiple accessMaterials Science (miscellaneous)Bandwidth (signal processing)Optical communicationSpatial codeMultiplexingIndustrial and Manufacturing EngineeringOpticsElectronic engineeringBusiness and International ManagementbusinessOptical filterImage resolutionApplied optics
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