Search results for "EXCHANGE"

showing 10 items of 2035 documents

Cu-B alloy - analysis of use possibility as fuel cell cathode catalyst

2016

In recent years there has been a development of non-conventional and renewable sources of energy. One such sources of energy are fuel cells. Fuel cells are ecological and high efficiency sources of electric energy. However, the use of fuel cells on a large scale is limited, mainly by the high cost of catalysts. Platinum is most commonly used as the catalyst. But due to the high price of platinum there’s a need for finding other catalysts. Replacement of platinum will contribute to the fast development of green energy sources. This paper presents a study of possibility of using Cu-B alloy as catalyst for oxygen electrode in fuel cells. Researches were done in glass vessel, on a copper electr…

cathodeMaterials scienceenvironmental engineeringAlloyMetallurgyProton exchange membrane fuel cellengineering.materialDirect-ethanol fuel cellCathode catalystfuel cellCu-B alloyoxygen electrodeengineeringFuel cellsrenewable energy sourcesQUAESTI-Virtual Multidisciplinary Conference
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Tri- and tetranuclear heteropivalate complexes with core {Fe2Ni O} (x = 1, 2): Synthesis, structure, magnetic and thermal properties

2019

Abstract The reactions of complex [Fe2Ni(O)(Piv)6(Et2O)(H2O)2] (1) with 1,10-phenanthroline (phen) and 2,2′-bipyridine (bpy) gave the following new coordination compounds: the trinuclear complex [Fe2Ni(O)(Piv)6(phen)H2O]·(C2H5)2O (2), the tetranuclear ones [Fe2Ni2(OH)2(Piv)8(phen)2] (3) and [Fe2Ni2(OH)2(Piv)8(bpy)2] (4), depending on the crystallization conditions. According to single crystal X-ray diffraction data, all the compounds have molecular structures. The Mossbauer spectra of 1–3 correspond to high-spin Fe3+ ions in an octahedral environment consisting of oxygen atoms. The DC magnetic susceptibility studies and quantum-chemical analysis of intra- and intermolecular J pathways using…

chemistry.chemical_classification010405 organic chemistryThermal decomposition010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesCoordination complexInorganic ChemistryCrystallographychemistryOctahedronSuperexchangeMaterials ChemistryAntiferromagnetismDensity functional theoryPhysical and Theoretical ChemistrySingle crystalPolyhedron
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Synthesis and characterization of new coordination compounds by the use of 2-pyridinemethanol and di- or tricarboxylic acids

2021

The development of synthetic approaches towards new coordination polymers has attracted significant interest due to their fascinating physical properties, as well as their use in a wide range of technological, environmental and biomedical applications. Herein, the initial combination of 2-pyridinemethanol (Hhmp) with 1,4-benzenedicarboxylic acid (H2bdc) or 1,3,5-benzenetricarboxylic acid (H3btc) has been proven a fruitful source of such new species providing access to five new coordination compounds, namely [M2(Hbtc)2(Hhmp)4]·DMF (M = CoII, 1·DMF;NiII, 2·DMF), [Ni(bdc)(Hhmp)2]n·4H2O (3·4H2O), [Zn2(bdc)(hmp)2]n·DMF (4·DMF) and [Fe3(bdc)3(Hhmp)2]n (5). 4·DMF and 5 are the first metal–organic …

chemistry.chemical_classification02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMagnetic susceptibilityAntiferromagnetic coupling0104 chemical sciencesCoordination complexCrystallographychemistrySuperexchangeGeneral Materials Science0210 nano-technologyCrystEngComm
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Synthesis, crystal structure and magnetic properties of bis[μ-bis(3-(pyridin-2-yl)-1,2,4-triazole-N′,N1,N2)] bis[triaqua nickel(II)] tetranitrate

1998

Abstract A new dinuclear nickel(II) coordination compound of formula Ni2(Hpt)2(H2O)6(NO3)4 (Hpt=3-(pyridin-2-yl)-1,2,4-triazole) was synthesized. The structure was solved at 298 K by single-crystal X-ray analysis. Bisμ-bis(3-(pyridin-2-yl)-1,2,4-triazole-N′,N1,N2) bistriaqua nickel(II) tetranitrate (C14H24N12O18Ni2) crystallizes in the triclinic space group P-1, a=7.2266(1), b=9.9144(1), c=11.2647(1) A, α=66.854(1)°, β=74.000(1)°, γ=86.400(2)°, V=712.42(1) A3, Z=1 (dinuclear units), 2823 reflections (1 > 2σ(I)), R1=0.0442, wR2=0.1197. The Ni(II) ions are bridged by two neutral Hpt ligands coordinating via N1 and N2 in the equatorial plane, Ni(1)-Ni(1)′=4.098(1) A. The Hpt bridging mode is a…

chemistry.chemical_classification124-Triazolechemistry.chemical_elementCrystal structureTriclinic crystal systemCoordination complexInorganic Chemistrychemistry.chemical_compoundNickelCrystallographychemistryOctahedronSuperexchangeMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
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Behavior of Actinium, Alkaline, and Rare Earth Elements in Sr-Resin/Mineral Acid Systems

2015

In this work, the interactions between the divalent alkaline earth elements (AEE) (Sr, Ba, Ra), the trivalent rare earth elements (REE) (Ce-Lu, Y), and Ac(III) with Sr-resin were investigated in the presence of HNO3, HCl, HBr, HClO4, and HPF6. Distribution coefficients of these ions on the Sr-resin were determined under batch-loading conditions. Lastly, online column separations were performed to demonstrate the utility of these systems. Substantial differences in the behavior of the ions in solutions comprised of the five different acids were observed. These differences can partly be explained by a combination of ion exchange (primary) and extraction (solvation) mechanisms. From a practica…

chemistry.chemical_classificationAlkaline earth metalIon exchangeGeneral Chemical EngineeringExtraction (chemistry)Inorganic chemistrySolvationchemistry.chemical_elementMineral acidGeneral ChemistryDivalentIonActiniumchemistrySolvent Extraction and Ion Exchange
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Application of a weakly basic dimethylamino-modified silica ion exchanger to the separation of oligonucleotides

1979

Abstract LiChrosorb RP-8, RP-18 and Diol as well as a newly synthesized basic dimethylamino-modified silica ion-exchanger (DMA-silica) were applied for the separation of adenylic acid, cytidylic acid and uridylic acid oligoribonucleotides. On LiChrosorb RP-8 and RP-18, respectively, in aqueous buffered eluents (K 2 HPO 4 - H 3 PO 4 ), the retention of oligonucleotides was increased with decreasing number of nucleotide units in the solute, i.e., with increasing hydrophobic character. The elution behaviour of ologonucleotides on LiChrosorb Diol followed the same order but took place according to a size-exclusion mechanism. The retention of oligonucleotides on DMA-silica is assumed to be based…

chemistry.chemical_classificationChromatographyAqueous solutionIon exchangeElutionOrganic ChemistryDiolIonic bondingSalt (chemistry)General MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryOligoribonucleotidesNucleotideJournal of Chromatography A
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Hydrophobic and cation exchange mechanisms in the retention of basic compounds in a polymeric column.

2004

A cation exchange retention mechanism concomitant with the well-known hydrophobic partition mechanism in a polymeric column has been observed and investigated. This exchange process is attributed to ionization of some acidic sites present in the polymer column at basic mobile phase pH values. Several drugs of different basicity have been chromatographed on a polymeric PLRP-S column with methanol-water and acetonitrile-water mobile phases. The cation exchange between the protonated basic drug and the buffer cations (Na+, K+ and BuNH4+) is observed at the pH range where the protonated drug and the ionized sites of the column coexist. This process produces a shift of the retention versus pH pl…

chemistry.chemical_classificationChromatographyBase (chemistry)ChemistryPolymersOrganic ChemistryProtonationGeneral MedicinePolymerHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectIonizationPhase (matter)Cation Exchange ResinsColumn (data store)Journal of chromatography. A
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The determination of the DNA base composition in 19 species of adriatic sponges with high-pressure liquid cation-exchange chromatography.

1976

Abstract The (adenine + thymine)/(guanine + cytosine) base ratios of 19 species of adriatic sponges have been determined by high-pressure liquid cation-exchange chromatography. The base ratios vary from 1.49 (Mycale massa) to 0.63 (Hippospongia communis) according to an (A+T) content of 59.7 and 38.6 mol%, respectively. The DNAs of sponges of the order Keratosa showed marked differences in their (A +T) contents (39.5 to 58.8 mol%) whereas those of Tetractinellida and Halichondrina were nearly identical (39.3 to 40.8 and 49.5 to 49.8 mol%, respectively). The 5-methylcytosine (5MC) content was determined in 8 sponge DNAs by a semiquantitative method. The values differed from 0.8 to 2.2 mol% o…

chemistry.chemical_classificationChromatographyBase (chemistry)GuanineIon chromatographyDeoxyribonucleosidesDNABiologybiology.organism_classificationChromatography Ion ExchangeHigh-performance liquid chromatographyGeneral Biochemistry Genetics and Molecular BiologyThyminePoriferachemistry.chemical_compoundSpongechemistryAnimalsComposition (visual arts)CytosineChromatography High Pressure LiquidZeitschrift fur Naturforschung. Section C, Biosciences
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The second component of human complement: Detection of two hemolytic forms in plasma by pH Variation

1988

The second component of human complement (C2) in pseudoglobulin prepared from normal plasma eluted as a single peak at high conductivity (30 mS) and pH 4.5 from the cationic exchangers S-Sepharose or Mono S in the Fast Protein Liquid Chromatography (FPLC) System. The C2 was stable at pH 4.5 and 0 degrees C if enzyme inhibitors were used and the pH was raised to 6.0 after elution from the columns. After rechromatography on Mono S in the FPLC System at the median isoelectric point of 5.5 or pH 6.0, the C2 eluted as two distinct hemolytic forms: the first peaked at 16 mS, the second at 30 mS. The two forms of C2 did not correlate with the allotypic variant of C2 in individual, normal human pla…

chemistry.chemical_classificationChromatographyElutionImmunologySize-exclusion chromatographyComplement C4Enzyme-Linked Immunosorbent AssayFast protein liquid chromatographyHematologyComplement C1 Inactivator ProteinsComplement C2Hydrogen-Ion ConcentrationChromatography Ion ExchangeHemolysisComplement factor Bchemistry.chemical_compoundIsoelectric pointEnzymeBiochemistrychemistryAlternative complement pathwayHumansImmunology and AllergySodium dodecyl sulfateImmunobiology
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Characterization of aquatic humic substances and their metal complexes by immobilized metal-chelate affinity chromatography on iron(III)-loaded ion e…

2001

The analytical fractionation of aquatic humic substances (HS) by means of immobilized metal-chelate affinity chromatography (IMAC) on metal-loaded chelating ion exchangers is described. The cellulose HYPHAN, loaded with different trivalent ions, and the chelate exchanger Chelex 100, loaded to 90% of its capacity with Fe(III), were used. The cellulose HYPHAN, loaded with 2% Fe(III), resulted in HS distribution coefficients Kd of up to 10(3.7) mL/g at pH 4.0 continuously decreasing down to 10(1.5) at pH 12, which were appropriate for HS fractionation by a pH-depending chromatographic procedure. Similar distribution coefficients Kd were obtained for HS sorption onto Fe(III)-loaded Chelex 100. …

chemistry.chemical_classificationChromatographyIon exchangeElutionIronSorptionFractionationReference StandardsChromatography Ion ExchangeBiochemistryChromatography Affinitychemistry.chemical_compoundChelex 100chemistryMetalsSpectroscopy Fourier Transform InfraredHumic acidSpectrophotometry UltravioletChelationCelluloseHumic SubstancesWater Pollutants ChemicalChelating AgentsFresenius' Journal of Analytical Chemistry
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