Search results for "bond"

showing 10 items of 3527 documents

Vacuum-ultraviolet absorption of interstitial O2 and H2O molecules in SiO2 glass

2006

Abstract Vacuum-ultraviolet (VUV) absorption of O 2 and H 2 O molecules incorporated in interstitial voids in SiO 2 glass by thermal annealings was examined. Interactions of the interstitial molecules with the surrounding SiO 2 glass network lead to a redshift of the VUV absorption band of interstitial O 2 , while a blueshift of that of interstitial H 2 O, both accompanied by an increase in the intensity of the absorption bands. The Coulomb repulsion, London dispersion, and hydrogen bonding are the main interactions responsible for the modification of the VUV absorption bands.

Absorption spectroscopyHydrogen bondbusiness.industryChemistryCondensed Matter PhysicsPhotochemistryLondon dispersion forceRedshiftElectronic Optical and Magnetic MaterialsBlueshiftOpticsAbsorption bandMaterials ChemistryCeramics and CompositesMoleculeAbsorption (chemistry)businessJournal of Non-Crystalline Solids
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An increased F2-laser damage in ‘wet’ silica glass due to atomic hydrogen: A new hydrogen-related E′-center

2006

Abstract A dramatic increase of F2-laser induced room temperature-stable point defects in ‘wet’ synthetic silica glass occurs when irradiation temperature is lowered to 80 K. Contrary to the predictions based on the established models of defect processes, a large part of defects induced at 80 K remains stable also at the room temperature. The intensities of the laser-induced optical absorption bands of the non-bridging oxygen hole centers (2.0 and 4.8 eV) and E′-centers (5.8 eV) are comparable to those created by neutron irradiation (1018 n/cm2). A growth of infrared absorption peak at 2237 cm−1 indicates creation of silicon hydride (SiH) groups. A study of irradiation dose dependences and …

Absorption spectroscopyHydrogenSiliconHydrideDangling bondAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsChemical bondchemistryExcited stateMaterials ChemistryCeramics and CompositesIrradiationJournal of Non-Crystalline Solids
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Temperature effects on the IR absorption bands of hydroxyl and deuteroxyl groups in silica glass

2009

Abstract In this report we will show the changes of the band shape of the hydroxyl group (SiOH) infrared (IR) absorption band (∼3670 cm −1 ) in silica glass induced by lowering temperature in the range from 290 to 20 K. This band is considered as the overlap of several spectral components associated to the vibrational activity of hydroxyl groups in different bond configurations. By a suitable analysis of the experimental band profile in terms of different sub-bands, we studied the thermal evolution of each component and we reconsidered their assignations. For comparison we examined the SiOD absorption band (∼2710 cm −1 ) as a function of temperature as well. Our data can be interpreted as a…

Absorption spectroscopyInfraredChemistryHydrogen bondFTIR measurements Infrared properties Silica AerogelsAnalytical chemistryInfrared spectroscopyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsExtinction (optical mineralogy)Absorption bandMolecular vibrationThermalMaterials ChemistryCeramics and Composites
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Interactions of amino acids with aluminum octacarboxyphthalocyanine hydroxide. Experimental and DFT studies

2017

The influence of albumin and amino acids (l-serine, glycine, l-histidine, l-tryptophan, l-cysteine) on the properties of aluminum octacarboxyphthalocyanine hydroxide (Al(OH)PcOC) was investigated in a phosphate buffer (pH 8.0). Particular attention was paid to the spectroscopic properties and photostability of Al(OH)PcOC. The effect of albumin or amino acids on the photodegradation of Al(OH)PcOC was examined in water using red light: 685 nm and daylight irradiation. Analysis of kinetic curves indicated that interaction with those molecules increases the photostability of Al(OH)PcOC. The molecular structure of Al(OH)PcOC complexes (in vacuum and in water) with axially or equatorially coordin…

Absorption spectroscopyInorganic chemistry02 engineering and technologyDFT calculations010402 general chemistryDFT01 natural sciencesPhotodynamic therapyCatalysisInorganic ChemistryAluminum octacarboxyphthalocyanine hydroxidechemistry.chemical_compoundMoleculePhysical and Theoretical ChemistryPhotodegradationchemistry.chemical_classificationamino acidsOriginal PaperChemistryHydrogen bondProteinOrganic Chemistry021001 nanoscience & nanotechnologyAmino acid0104 chemical sciencesComputer Science ApplicationsAmino acidTD-DFT spectraCrystallographyComputational Theory and MathematicsPhthalocyanineHydroxideDensity functional theory0210 nano-technologyJournal of Molecular Modeling
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EXAFS and XANES Studies of CoxMg1−xO Solid Solutions Using a Laboratory EXAFS Spectrometer

1993

Studies of the local electronic structure and the short-range order in solid solutions CoxMg1−xO with x varying from 0.02 to 1.00 are carried out on the CoK-edge X-ray absorption spectra using a laboratory EXAFS spectrometer. A non-monotonous change of the CoO distance in the first coordination shell with a bent at about x = 0.5 is established. The second coordination shell of cobalt is formed by cobalt and magnesium atoms with a distribution close to a statistical one. [Russian Text Ignored.]

Absorption spectroscopySpectrometerExtended X-ray absorption fine structureInorganic chemistryAnalytical chemistrychemistry.chemical_elementElectronic structureCondensed Matter PhysicsXANESElectronic Optical and Magnetic MaterialsBond lengthchemistryCobaltSolid solutionPhysica Status Solidi (a)
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Electronic signature of the instantaneous asymmetry in the first coordination shell of liquid water

2013

Interpretation of the X-ray spectra of water as evidence for its asymmetric structure has challenged the conventional symmetric nearly-tetrahedral model and initiated an intense debate about the order and symmetry of the hydrogen bond network in water. Here, we present new insights into the nature of local interactions in water obtained using a novel energy decomposition method. Our simulations reveal that while a water molecule forms, on average, two strong donor and two strong acceptor bonds, there is a significant asymmetry in the energy of these contacts. We demonstrate that this asymmetry is a result of small instantaneous distortions of hydrogen bonds, which appear as fluctuations on …

Absorption spectroscopymedia_common.quotation_subjectShell (structure)FOS: Physical sciencesGeneral Physics and AstronomyCondensed Matter - Soft Condensed Matter010402 general chemistry01 natural sciencesAsymmetryMolecular physicsGeneral Biochemistry Genetics and Molecular BiologySpectral linePhysics - Chemical Physics0103 physical sciencesMoleculeCondensed Matter - Statistical Mechanicsmedia_commonChemical Physics (physics.chem-ph)PhysicsMultidisciplinaryStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsHydrogen bondGeneral ChemistryComputational Physics (physics.comp-ph)AcceptorSymmetry (physics)0104 chemical sciencesCondensed Matter - Other Condensed MatterSoft Condensed Matter (cond-mat.soft)Physics - Computational PhysicsOther Condensed Matter (cond-mat.other)
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Modelling Aspects in Accumulative Roll Bonding process by Explicit Finite Element Analysis

2013

Accumulative Roll-Bonding (ARB) process is a severe plastic deformation (SPD) process, capable of developing grains below 1 μm in diameter and improving mechanical properties of the material. In this study, the authors compared two different FE-codes with respect of its applicability for numerical analysis of the ARB process. Modelling this process was achieved using the explicit code for Abaqus/CAE both in 2D and 3D. The proposed model was used to assess the impact of ARB cycles on the final material properties. The numerical results in 2D and 3D were compared and contrasted. The research work presented in this paper is focused on the simulation optimization based on CPU time minimization.…

Accumulative Roll Bonding Aluminum alloy Material properties Explicit finite element analysis
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Experimental and robust modeling approach for lead(II) uptake by alginate gel beads: influence of the ionic strength and medium composition.

2014

Abstract Systematic kinetic and equilibrium studies on the lead ions removal ability by Ca-alginate gel beads have been performed by varying several internal parameters, namely, number of gel beads, nature and composition of the ionic medium and pH, which allowed us to model a wastewater in order to closely reproduce the composition of a real sample. Moreover, the effects brought about the different ionic species present in the reacting medium have been evaluated. Differential Pulse Anodic Stripping Voltammetry (DP-ASV), has been systematically used to perform kinetic and equilibrium measurements over continuous time in a wide range of concentration. Kinetic and equilibrium data have been q…

Accuracy and precisionChemistryAnalytical chemistryIonic bondingKinetic energySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonBiomaterialsAnodic stripping voltammetryColloid and Surface ChemistryIonic strengthAlginate gel beads Robust statistics Metal adsorption Wastewater treatment Ionic strength Differential Pulse Anodic Stripping Voltammetry Adsorption isotherms Adsorption kinetics Lead Heavy metalmedicineComposition (visual arts)Settore CHIM/01 - Chimica AnaliticaSwellingmedicine.symptomJournal of colloid and interface science
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The modelling of the cathode sheath of an electrical arc in vacuum

2003

This paper presents a simple model of the fragment in the cathode electrical arc root taking into account the physical phenomena occuring on the cathode surface and the sheath. The goal is the obtainment of characteristics values of the heat flux, the electrons, and atoms density in the sheath. Computation is carried out on a one-dimensional model with a coupling between the equation obtained in the sheath and an enthalpy model of the cathode to describe the temperature evolution. In the modelling, we introduce a friction zone above the sheath edge to characterize the heavy particle interactions. Numerical simulation shows that the ionic friction phenomenon deriving from ion–atom collision …

Acoustics and UltrasonicsvacuumIonic bondingarc rootheat fluxElectroncathode sheatharc01 natural sciences010305 fluids & plasmaslaw.inventionElectric arcCross section (physics)lawPhysics::Plasma Physics[PHYS.PHYS.PHYS-PLASM-PH]Physics [physics]/Physics [physics]/Plasma Physics [physics.plasm-ph]0103 physical sciences010306 general physicsCouplingComputer simulationChemistryMechanics[ PHYS.PHYS.PHYS-PLASM-PH ] Physics [physics]/Physics [physics]/Plasma Physics [physics.plasm-ph]Condensed Matter PhysicsCathodeSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHeat flux
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Amphotropic Ionomers by Attachment of Secondary Amines to a Reactive Ester Polymer

2004

We report on the synthesis of polyacrylamides that were prepared by the reaction of a reactive ester polymer with a mesogen-containing secondary amine and N-methyl-piperazine. As the polymers do not form hydrogen bonds near the amide groups, their mobility is significantly higher than that of poly(N-monoalkylacrylamides). The initially nonionic polymer shows no liquid-crystalline behavior in bulk and in mixture with ethylene glycol. This is due to the low polarity difference between the different side chains. The polarity difference can be increased by protonation or quarter-nization of the tertiary amino groups, and liquid-crystalline behavior is observed. The self-assembly multilayer buil…

Acrylate polymerchemistry.chemical_classificationPolymers and PlasticsHydrogen bondOrganic ChemistryPolymerCondensed Matter PhysicsPolyelectrolytechemistry.chemical_compoundchemistryAmidePolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryEthylene glycolIonomerMacromolecular Chemistry and Physics
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