Search results for "EXCHANGE"

showing 10 items of 2035 documents

Selective extraction of small proteins from biological samples using a novel restricted access column with cation exchange properties

2000

The determination of proteins utilising a polymer-based restricted access suppor material with ion exchange properties (IERAM) is outlined. Solid phase extraction coupled on-line with a mincrobore reversed phase HPLC system for the quantitation of small marker proteins is demonstrated. The cation-exchange restricted access packings were characterised with respect to their adsorption and desorption kinetics. The IERAM material was also investigated by capacity, selectivity, and biocompatibility determinations when applied to the quantification of small molecular weight proteins such as cytochrome C, Lysozyme, Ribonuclease A, Myoglobin, Insulin, human serum albumin, and a Tryptic inhibitor.

chemistry.chemical_classificationChromatographyIon exchangebiologyChemistryOrganic ChemistryClinical BiochemistryExtraction (chemistry)PolymerReversed-phase chromatographyHuman serum albuminBiochemistryAnalytical ChemistryMatrix-assisted laser desorption/ionizationmedicinebiology.proteinPancreatic ribonucleaseSolid phase extractionmedicine.drug
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Comparative study for separation of aquatic humic-type organic constituents by DAX-8, PVP and DEAE sorbing solids and tangential ultrafiltration: ele…

2005

Aquatic humic-type solutes were separated in parallel from the same fresh water source by four different procedures: non-ionic polymethyl methacrylate (DAX-8) and functional cross-linked polyvinylpyrrolidone (PVP) resins, functional diethylaminoethyl cellulose (DEAE) and tangential ultrafiltration completed with a weakly basic anion exchange resin (IRA-67). The similarity-dissimilarity between the quantities and qualities of the different humic samples is discussed, especially in the light of the original dissolved organic matter (DOM). During the past two decades, a significant progress has occurred in the aquatic humic research due to the so-called hydrophobic-hydrophilic properties posse…

chemistry.chemical_classificationGel permeation chromatographyChromatographychemistrySize-exclusion chromatographyDiethylaminoethyl celluloseDissolved organic carbonUltrafiltrationOrganic matterIon-exchange resinDEAE-CelluloseAnalytical ChemistryTalanta
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RAS proteins and control of the cell cycle inSaccharomyces cerevisiae

1995

Genes related to the mammalian H-, K-, and N-ras oncogenes were identified in S. cerevisiae by DNA hybridization techniques (for reviews, see Tamanoi, 1988; Gibbs and Marshall, 1989; Broach and Deschenes, 1990). According to the rules of yeast genetics (dominant genes are indicated by three capital letters followed by a number), the yeast genes were denominated RAS1 and RAS2 (collectively referred to as RAS). The corresponding RAS1 and RAS2 proteins were 309 and 322 amino acids long, respectively. The sequence similarity between the human and yeast proteins was very high, reaching 90% identity at the level of the N-terminal 80 amino acids. As a consequence, perfect sequence conservation was…

chemistry.chemical_classificationGeranylgeranyl TransferaseBiochemistrybiologychemistryDNA–DNA hybridizationSaccharomyces cerevisiaeGuanine nucleotide exchange factorRas2biology.organism_classificationGeneYeastAmino acid
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Equilibrium and transport properties of ion-exchange membranes

1984

Abstract Specific properties (ion-exchange capacity, water content, pore volume fraction) and transport properties (counterion transport number and electrical conductivity) have been measured in four commercial cation-exchange membranes loaded with a variety of cations of different nature and charge. Not surprisingly, equivalent conductances are lower than in free solution and transport numbers decrease with valency of the counterion. This behavior is explained by taking into account a “tortuosity factor”, due to a lengthening of the pores across the membrane, except for a membrane with a lower water content and for ions of higher charge, in which electrostatic interactions between mobile a…

chemistry.chemical_classificationIon exchangeInorganic chemistryFiltration and SeparationElectrostaticsBiochemistryIonMembranechemistryElectrical resistivity and conductivityChemical physicsVolume fractionGeneral Materials SciencePhysical and Theoretical ChemistryCounterionPorosityJournal of Membrane Science
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Distribution and mobility of phosphates and sodium ions in cheese by solid-state 31 P and double-quantum filtered 23 Na NMR spectroscopy

2010

The feasibility of solid-state magic angle spinning (MAS) (31)P nuclear magnetic resonance (NMR) spectroscopy and (23)Na NMR spectroscopy to investigate both phosphates and Na(+) ions distribution in semi-hard cheeses in a non-destructive way was studied. Two semi-hard cheeses of known composition were made with two different salt contents. (31)P Single-pulse excitation and cross-polarization MAS experiments allowed, for the first time, the identification and quantification of soluble and insoluble phosphates in the cheeses. The presence of a relatively 'mobile' fraction of colloidal phosphates was evidenced. The detection by (23)Na single-quantum NMR experiments of all the sodium ions in t…

chemistry.chemical_classificationIon exchangeSodium0402 animal and dairy scienceAnalytical chemistrychemistry.chemical_elementSalt (chemistry)04 agricultural and veterinary sciencesGeneral ChemistryNuclear magnetic resonance spectroscopy040401 food science040201 dairy & animal scienceIonColloid0404 agricultural biotechnologychemistryMagic angle spinningGeneral Materials ScienceSpectroscopyMagnetic Resonance in Chemistry
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Adsorption of gaseous p-xylene and m-xylene on NaY, KY, and BaY zeolites: Part 1. Adsorption equilibria of pure xylenes

1995

Abstract Isothermal and isobaric adsorptions of p -xylene and m -xylene on NaY, KY, and BaY are studied by thermogravimetry between 25°C and 400°C, and 10 Pa and 1014 Pa. At low filling BaY shows a stronger affinity for xylenes than the other zeolites. At high temperature and low pressure its adsorption capacity is greater than those of NaY and KY. These two zeolites have a similar behavior and adsorb more m -xylene than p -xylene. At low temperature and high pressure KY adsorbs p -xylene like NaY and m -xylene like BaY, and, unlike NaY, the adsorption capacities of KY and BaY are higher for p -xylene than for m -xylene. The substitution of K + or Ba 2+ for Na + decreases the adsorption cap…

chemistry.chemical_classificationIon exchangeXyleneInorganic chemistryAnalytical chemistrym-Xylenep-XyleneThermogravimetrychemistry.chemical_compoundHydrocarbonAdsorptionchemistryZeoliteGeneral Environmental ScienceZeolites
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Structural and magnetic properties of polynuclear oximate copper complexes with different topologies

2017

Abstract Two new copper(II) complexes containing the methyl(2-pyridyl)ketone oxime ligand (mpkoH) [Cu3(OH)(ClO4)2(mpko)3]·CH3OH (1) and [Cu(ClO4)(mpko)(mpkoH)]n (2) have been prepared from Cu(ClO4)2 and mpkoH in different metal-to-ligand molar ratios. In addition, the compound [Cu{(mpko)2BF2}(H2O)](BF4) (3) [(mpko)2BF2 is the fluoroboration product of the oxime] has been obtained when replacing Cu(ClO4)2 by Cu(BF4)2. Compound 1 is an isolated triangle with a {Cu3(µ3-OH)}5+ core, whereas 2 is a chain of CuII ions linked by anionic mpko− bridges. 1 exhibits strong antiferromagnetic competing interactions, as well as antisymmetric exchange. On the other hand, very weak ferromagnetic interactio…

chemistry.chemical_classificationKetoneAntisymmetric exchange010405 organic chemistryLigandInorganic chemistrychemistry.chemical_element010402 general chemistryOxime01 natural sciencesCopper0104 chemical scienceslaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerromagnetismlawMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryElectron paramagnetic resonancePolyhedron
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Design and characterization of bi-functional electrocatalytic layers for application in PEM unitized regenerative fuel cells

2010

Abstract Results concerning the development and characterization of bi-functional electrocatalytic layers for application in unitized regenerative fuel cells (URFCs) based on proton exchange membrane (PEM) technology are reported. Carbon-supported hydrophobic (10 wt.% of PTFE) Pt catalysts (40 wt.% of Pt), and Pt and Ir black powders of large specific areas have been synthesized. Their structure, morphology and electrochemical properties have been investigated using SEM, TEM, XRD analysis, and by measurements of polarization curves and cyclic voltammograms. Current–voltage curves have been recorded during water electrolysis and H 2 /O 2 fuel cell experiments to evaluate their performances a…

chemistry.chemical_classificationMaterials scienceElectrolysis of waterRenewable Energy Sustainability and the EnvironmentAnalytical chemistryEnergy Engineering and Power TechnologyProton exchange membrane fuel cellPolymerCondensed Matter PhysicsElectrochemistryAnodeCatalysisFuel TechnologyMembraneChemical engineeringchemistryPolarization (electrochemistry)International Journal of Hydrogen Energy
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A Self-Assembled 2D Molecule-Based Magnet: The Honeycomb Layered Material {Co3Cl4(H2O)2[Co(Hbbiz)3]2}

2003

Research in the area of molecule-based magnets is rapidly expanding, owing, in part, to numerous breakthroughs in the past decade.[1] The preparation of solid-state architectures of varying dimensionalities from specifically tailored paramagnetic building blocks has proven to be very successful, and also clearly multidisciplinary. Materials science and supramolecular chemistry efforts have joined forces with classical organic and inorganic chemistry in the design of solid-state materials whose magnetic properties rival, and sometimes even exceed, those of classic inorganic solids.[2] The moleculebased strategy allows for the preparation of unusual materials that cannot otherwise be obtained…

chemistry.chemical_classificationMaterials scienceInorganic chemistrySupramolecular chemistryOxideGeneral ChemistryCatalysisCoordination complexchemistry.chemical_compoundParamagnetismchemistryChemical physicsSuperexchangeMagnetMoleculeDicyanamideAngewandte Chemie International Edition
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Proton Conducting Membrane Prepared by Cross-Linking Highly Sulfonated Peek for PEMFC Application

2009

The proton conducting membrane was prepared by cross-linking highly sulfonated and sulfinated poly(etheretherketone) (SsPEEK). The cross-linked membrane is low cost due to its use of non-expensive chemical and simple production procedure. The membrane exhibited high proton conductivity (0.04 S/cm at 60 °C), extremely reduced water uptake, enhanced strength and stability compared with that of non-cross-linked membrane. These results suggested that the cross-linked PEEK membrane is a suitable candidate of proton conducting membranes for polymer electrolyte membrane fuel cell (PEMFC) applications, particularly promising to be used in direct methanol fuel cell (DMFC) due to its lower methanol c…

chemistry.chemical_classificationMaterials scienceProton exchange membrane fuel cellElectrolytePolymerConductivitychemistry.chemical_compoundDirect methanol fuel cellMembranechemistryChemical engineeringPeekMethanolNuclear chemistryASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology
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