Search results for " alloy"

showing 10 items of 1757 documents

Grooving by Nd:YAG laser treatment

2000

Abstract The properties of the laser beam have been used to produce deep and thin grooves in metals, melted material being removed with the assistance of a high velocity gas. Preliminary experiments show that the geometry and the location of the gas inlet tube are the main parameters governing the evacuation of the scoria. The influence of the nature of the materials on the depth of the grooves is discussed from examination of the grooves realized on various metals (copper, aluminum, titanium,…). Finally, a statistical study is performed to indicate the parameters that have to be controlled to secure regular grooves. It appears that the groove width is not too much affected by parameter var…

geographyJet (fluid)geography.geographical_feature_categoryMaterials sciencebusiness.industryMetals and Alloyschemistry.chemical_elementInletCopperIndustrial and Manufacturing EngineeringComputer Science ApplicationsOpticschemistryAluminiumModeling and SimulationNd:YAG laserCeramics and CompositesTube (container)ScoriabusinessTitaniumJournal of Materials Processing Technology
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Speciation and interactions of plutonium with humic substances and kaolinite in aquifer systems

2007

Abstract The speciation of plutonium (Pu) in contact with humic substances (HS) and kaolinite has been performed in aquifer systems. Mainly the redox behavior, complexation, and sorption of plutonium are discussed here. The redox behavior of Pu(VI) in contact with HS was studied and it was found that Pu(VI) is reduced to Pu(III) and Pu(IV) within a couple of weeks. The complexation constants (log  β LC ) of Pu(III) and Pu(IV) with HS have been determined by means of the ultrafiltration method. Furthermore, the sorption of Pu(III) and Pu(IV) onto kaolinite has been investigated as a function of pH by batch experiments under aerobic and anaerobic conditions.

geographygeography.geographical_feature_categoryChemistryMechanical Engineeringmedia_common.quotation_subjectMetals and AlloysUltrafiltrationchemistry.chemical_elementAquiferSorptionRedoxPlutoniumSpeciationMechanics of MaterialsMaterials ChemistryKaoliniteNuclear chemistrymedia_commonJournal of Alloys and Compounds
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Very strong −N–X+⋯−O–N+ halogen bonds

2016

A new (-)N-X(+)(-)O-N(+) paradigm for halogen bonding is established by using an oxygen atom as an unusual halogen bond acceptor. The strategy yielded extremely strong halogen bonded complexes with very high association constants characterized in either CDCl3 or acetone-d6 solution by (1)H NMR titrations and in the solid-state by single crystal X-ray analysis. The obtained halogen bond interactions, RXB, in the solid-state are found to be in the order of strong hydrogen bonds, viz. RXB ≈ RHB.

halogen bondsNanotechnologychemistry010402 general chemistry01 natural sciencesCatalysisoxygen atomMaterials Chemistryta116Halogen bond010405 organic chemistryChemistryHydrogen bondMetals and AlloysGeneral ChemistryAcceptor0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyOxygen atomHalogenCeramics and CompositesProton NMRTitrationSingle crystalChemical Communications
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Features of W production in p-p, p-Pb and Pb-Pb collisions

2017

We consider the production of inclusive W bosons in variety of high-energy hadronic collisions: p--p, p--$\overline{\rm p}$, p--Pb, and Pb--Pb. In particular, we focus on the resulting distributions of charged leptons from W decay that can be measured with relatively low backgrounds. The leading-order expressions within the collinearly factorized QCD indicate that the center-of-mass energy dependence at forward/backward rapidities should be well approximated by a simple power law. The scaling exponent is related to the small-$x$ behaviour of the quark distributions, which is largely driven by the parton evolution. An interesting consequence is the simple scaling law for the lepton charge as…

heavy ion: scatteringHadronPb-Pb collisionsPartonElementary particle02 engineering and technologycomputer.software_genrePower lawHigh Energy Physics - ExperimentHigh Energy Physics - Experiment (hep-ex)background: lowHigh Energy Physics - Phenomenology (hep-ph)0202 electrical engineering electronic engineering information engineering[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]050107 human factorsBosonQuantum chromodynamicsPhysicsDatabasehigher-order: 0Hadronic collisionsCharge asymmetries05 social sciencesscalinghep-phCharged leptonsHigh Energy Physics - PhenomenologyCERN LHC CollParticle Physics - ExperimentQuarkInelastic scatteringParticle physicssmall-xquark: distribution functionp p: scatteringFOS: Physical sciencesW: decay114 Physical sciencesenergy dependence[ PHYS.HEXP ] Physics [physics]/High Energy Physics - Experiment [hep-ex]W: productionquantum chromodynamicsanti-p p: scatteringCollision systems0501 psychology and cognitive sciencesHigh energy physicsp nucleus: scatteringBosonsParticle Physics - Phenomenologyhep-exlepton: charge: asymmetryfactorization: collinearHigh Energy Physics::PhenomenologyElementary particlesScaling exponent Lead alloys020207 software engineeringBinary alloysW bosonsLeading ordersrapidityevolution equation[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph][ PHYS.HPHE ] Physics [physics]/High Energy Physics - Phenomenology [hep-ph]High Energy Physics::Experimentcomputerhigh-energy hadronic collisionsLead Center-of-mass energiesLepton
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Reduction and catalytic behaviour of heterobimetallic copper–lanthanide oxides

2008

Abstract The reduction of the heterobimetallic copper–lanthanide oxides 2CuO·CeO2 and 3CuO·Ln2CuO4 (Ln = La, Pr, Nd) was studied by H2-TG/DTA and H2-TPR. All systems exhibit two main reduction steps accompanied by mass losses in the temperature range 20–1000 °C. The first step was attributed to CuO reduction, whereas the second step is due either to copper reduction in the Ln2CuO4 phase with the concomitant formation of Ln2O3 or to the surface reduction of CeO2. The products were characterized by XRD, SEM, EDX, and BET techniques and are better described as supported copper type materials. They were active for the mesityl oxide (4-methyl-2-penten-2-one) gas phase hydrogenation.

heterobimetallic copper–lanthanide oxidesLanthanideCopper oxideInorganic chemistrychemistry.chemical_element02 engineering and technology[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysischemistry.chemical_compoundmesityl oxide hydrogenationMesityl oxideTransition metalDifferential thermal analysisMaterials ChemistryComputingMilieux_MISCELLANEOUSreduction studiesintermetallic compoundsMechanical EngineeringMetals and Alloys[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry021001 nanoscience & nanotechnologyCopper0104 chemical scienceschemistryMechanics of Materials0210 nano-technologyJournal of Alloys and Compounds
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Pneumococcal histidine triads – involved not only in Zn2+, but also Ni2+ binding?

2018

Polyhistidine triad proteins, which participate in Zn2+ uptake in Streptococcus pneumoniae, contain multiple copies of the HxxHxH (histidine triad motif) sequence. We focus on three such motifs from one of the most common and well-conserved polyhistidine triad proteins, PhtA, in order to understand their bioinorganic chemistry; particular focus is given to (i) understanding which of the PhtA triads binds Zn2+ with the highest affinity (and why) and (ii) explaining whether Ni2+ (also crucial for bacterial survival and virulence) could potentially outcompete Zn2+ at its native binding site. There is no significant difference in the stability of zinc(II) complexes with the three studied protei…

inorganic chemicals0301 basic medicineChemistry030106 microbiologySignificant differenceMetals and AlloysBiophysicsVirulenceBioinorganic chemistrymedicine.disease_causeBiochemistryBiomaterials03 medical and health sciencesBiochemistryChemistry (miscellaneous)Streptococcus pneumoniaemedicineBinding siteHistidineMetallomics
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Asymmetric [N–I–N]+halonium complexes in solution?

2020

Assessment of the solution equilibria of [bis(pyridine)iodine(I)]+ complexes by ESI-MS and NMR reveals the preference of iodine(I) to form complexes with a more basic pyridine. Mixtures of symmetric [bis(pyridine)iodine(I)]+ complexes undergo statistical ligand exchange, with a predominant entropic driving force favoring asymmetric systems. The influence of ligand basicity, concentration, temperature, and ligand composition is evaluated. Our findings are expected to facilitate the investigations, and the supramolecular and synthetic applications of halonium ions’ halogen bonds. peerReviewed

inorganic chemicals2019-20 coronavirus outbreakliuoksetLigandMetals and AlloysSupramolecular chemistrychemistry.chemical_elementliganditkompleksiyhdisteetGeneral ChemistryIodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonjodichemistry.chemical_compoundchemistryPyridineHalogenMaterials ChemistryCeramics and CompositesHalonium ionChemical Communications
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Surfactant-assisted synthesis of Cd1−xCoxS nanocluster alloys and their structural, optical and magnetic properties

2010

We report the synthesis of Co-doped CdS nanoclusters (Cd1−xCoxS) for different doping concentrations (x = 0.10, 0.20 and 0.30) and characterization of their structural, optical, and magnetic properties. The structural properties studied by X-ray diffraction revealed hexagonal-greenockite structure and a decrease of the lattice parameters (a and c) with doping, showing incorporation of Co in the lattice. The morphology of the nanoclusters was studied by scanning electron microscopy. The optical absorption studies, using diffused reflectance spectroscopy, revealed that Co doping modifies the absorption band edge. Ferromagnetic phase was observed in the magnetization measurements at room-tempe…

inorganic chemicalsAbsorption spectroscopyChemistryMechanical EngineeringDopingtechnology industry and agricultureMetals and AlloysAnalytical chemistryMagnetic semiconductorMicrostructureXANESNanoclustersCondensed Matter::Materials ScienceMagnetizationCrystallographyMechanics of MaterialsAbsorption bandMaterials Chemistrylipids (amino acids peptides and proteins)Condensed Matter::Strongly Correlated Electronshuman activitiesJournal of Alloys and Compounds
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Potent affinity material for tracing acetone and related analytes based on molecular recognition by halogen bonds.

2014

Affinity materials based on halogen bonds turned out to be a powerful tool for the molecular recognition of acetone or related carbonyl compounds in the presence of ubiquitous protic molecules. The superior selectivity and sensitivity were found by the gravimetric detection of volatile organic compounds by quartz crystal microbalances.

inorganic chemicalsAnalyteMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystalchemistry.chemical_compoundMolecular recognitionchemistryHalogenMaterials ChemistryCeramics and CompositesAcetoneMoleculeOrganic chemistryGravimetric analysisSelectivityChemical communications (Cambridge, England)
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Inhibitoren der Korrosion 25(1) - Über die Rolle der Kationen in Neutralsalzen bei der Korrosion von Eisenwerkstoffen in Gegenwart von Sauerstoff

1979

Die Geschwindigkeit des Sauerstoffverbrauchs bei der Korrosion von jeweils 500 mg DAB6-Eisenpulver wird in Abhangigkeit von der Art des Kations in Neutralsalzen (Chloriden) unter Standardbedingungen bestimmt. In Gegenwart von Alkali-, Quartaren Ammonium, Quartaren Phosphonium-und Erdalkalichloriden ist die Geschwindigkeit des Sauerstoffverbrauches vergleichbar gros. Mit Zink-, Cadmium-, Nickel-und Kobaltchloriden wird aber im Bereich von pH5 bis pH7 eine uberraschend grose Verzogerung der Sauerstoffaufnahme beobachtet. Es handelt sich mit hoher Wahrscheinlichkeit um eine Blockade der kathodischen Bezirke in der Eisengrenzflache durch Abscheidung der schwerloslichen basischen Hydroxyde von Z…

inorganic chemicalsCadmiumChemistryMechanical EngineeringMetals and Alloyschemistry.chemical_elementGeneral MedicineZincChlorideOxygenSurfaces Coatings and FilmsNickelchemistry.chemical_compoundMechanics of MaterialsMaterials ChemistrymedicineEnvironmental ChemistryAmmoniumPhosphoniumCobaltmedicine.drugNuclear chemistryMaterials and Corrosion/Werkstoffe und Korrosion
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