Search results for "Spectroscopy"

showing 10 items of 10293 documents

Study of interacting bands of silane: Analysis of infrared and Raman spectra

1990

Abstract The ν 1 ν 3 interacting bands of natural silane have been studied by Fourier transform spectroscopy and stimulated Raman spectroscopy, respectively, in the regions 2040–2320 and 2180–2187 cm−1. These data combined with available microwave observations have been analyzed using a reduced effective Hamiltonian developed through the fifth order for 28SiH4 and through the fourth order for 29SiH4 and 30SiH4. The observed infrared and Raman transitions have been very well reproduced with a standard deviation of about 0.0004 cm−1 for 28SiH4. Some anomalies in the Hamiltonian expansion have been found, but they did not perturb the analysis.

chemistry.chemical_classificationMaterials scienceInfraredbusiness.industryMolecular physicsSilaneAtomic and Molecular Physics and OpticsFourier transform spectroscopysymbols.namesakechemistry.chemical_compoundFourier transformOpticschemistrysymbolsPhysical and Theoretical ChemistryRaman spectroscopyHamiltonian (quantum mechanics)businessSpectroscopyInorganic compoundSpectroscopyJournal of Molecular Spectroscopy
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Structure and Chemical Bonds in Black Ti(C, N, O) Thin Films

2010

chemistry.chemical_classificationMaterials scienceMembrane protein interactions020206 networking & telecommunications02 engineering and technologyCrystal structuresymbols.namesakeCrystallographyChemical bondchemistryX-ray crystallography0202 electrical engineering electronic engineering information engineeringsymbols020201 artificial intelligence & image processingCompounds of carbonThin filmRaman spectroscopySpectroscopyAIP Conference Proceedings
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Dye-containing S∗cside-on/end-on copolymers

1995

Abstract Mesomorphic copolysiloxanes, which combine ‘normal’ end-on linked chiral mesogenic units inducing S∗c phases and side-on fixed chromophores were prepared. The interplay of the different orientational tendencies of these moieties, which are perpendicular (end-on linked mesogenic groups) or parallel (side-on fixed chromophores) to the polymer chain, lead to a strong destabilization of the S∗c phase. However, copolymers with up to about 10 mol % of chromophores still show a smectic C∗ phase. FTIR measurements show that both moieties orient parallel to each other and perpendicular to the polymer chains. These copolymers are interesting to consider as coloured guest-host S∗c materials f…

chemistry.chemical_classificationMaterials scienceMesogenGeneral ChemistryPolymerChromophoreCondensed Matter PhysicsCrystallographychemistryLiquid crystalPhase (matter)CopolymerPerpendicularOrganic chemistryGeneral Materials ScienceFourier transform infrared spectroscopyLiquid Crystals
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Covalently attached polymer mono- and multilayers on silanized glass substrates

1996

Abstract Applying grazing incidence FTIR and ellipsometry, the reaction of poly [(1-methyl-vinyl isocyanate)-alt-(maleic anhydride)](IAP) with amino-silanized glass and silicon oxide surfaces has been investigated. A reactive surface containing isocyanate and anhydride groups was formed after the adsorption of the polymer. The layer could be further functionalized using 2-aminoethanol. Multilayers could be built up by adsorbing a second layer of IAP onto an already reacted first layer of IAP.

chemistry.chemical_classificationMaterials scienceMetals and AlloysMaleic anhydrideSurfaces and InterfacesPolymerIsocyanateSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAdsorptionchemistrySilanizationPolymer chemistryMaterials ChemistryFourier transform infrared spectroscopySilicon oxideLayer (electronics)Thin Solid Films
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Structured Nanoparticles from the Self-Assembly of Polymer Blends through Rapid Solvent Exchange

2017

Molecular dynamics simulations were performed to study systematically the rapid mixing of a polymer blend in solution with a miscible nonsolvent. In agreement with experiments, we observe that polymers self-assemble into complex nanoparticles, such as Janus and core-shell particles, when the good solvent is displaced by the poor solvent. The emerging structures can be predicted on the basis of the surface tensions between the polymers as well as between the polymers and the surrounding liquid. Furthermore, the size of the nanoparticles can be independently tuned through the mixing rate and the polymer concentration in the feed stream; meanwhile, the composition of the nanoparticles can be c…

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventMolecular dynamicsChemical engineeringchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceParticle sizePolymer blendJanus0210 nano-technologySpectroscopyLangmuir
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On the Stability of Polymeric Nanoparticles Fabricated through Rapid Solvent Mixing.

2018

We study the stability of polymeric nanoparticles fabricated through the rapid mixing of polymers in a good solvent with a poor solvent that is miscible with the good solvent. In previous experiments where water was used as the poor solvent, a negative surface charge was measured on the precipitated nanoparticles, which led to the long-time stability of the dispersion. It was argued that these charges originate presumably from either water or hydroxide adsorption at the hydrophobic nanoparticle surface or from impurities in the feed streams that preferentially adsorb on the precipitated nanoparticles. To elucidate the origin of this stabilization mechanism, we performed experiments wherein …

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventchemistry.chemical_compoundAdsorptionChemical engineeringchemistryElectrochemistryHydroxideGeneral Materials ScienceSurface charge0210 nano-technologyDispersion (chemistry)SpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Interfacial Tensions from Drop Retraction versus Pendant Drop Data and Polydispersity Effects

2004

Interfacial tensions sigma were measured by means of both methods for the following polymer pair: polyisobutylene (PIB 3) plus poly(dimethylsiloxane) (PDMS 152) and poly(dimethyl-co-methylphenylsiloxane) (CoP26*) plus PDMS 48. The numbers after the abbreviation state the molar masses in kilograms; the homopolymers exhibit polydispersities on the order of 2. The reliability of the method of drop retraction is backed up by systematic measurements, which demonstrate that it is possible to study the time evolution of sigma. Because of the free choice of the phases (drop or matrix) and the possibility to vary the overall composition of the system in a wide range, drop retraction yields more info…

chemistry.chemical_classificationMaterials scienceMolar massDrop (liquid)DispersityTime evolutionThermodynamicsSurfaces and InterfacesPolymerCondensed Matter PhysicsDrop methodSurface tensionchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
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Effect of the supramolecular interactions on the nanostructure of halloysite/biopolymer hybrids: A comprehensive study by SANS, fluorescence correlat…

2020

The structural properties of halloysite/biopolymer aqueous mixtures were firstly investigated by means of combining different techniques, including small-angle neutron scattering (SANS), electric birefringence (EBR) and fluorescence correlation spectroscopy (FCS). Among the biopolymers, non-ionic hydroxypropylcellulose and polyelectrolytes (anionic alginate and cationic chitosan) were selected. On this basis, the specific supramolecular interactions were correlated to the structural behavior of the halloysite/biopolymer mixtures. SANS data were analyzed in order to investigate the influence of the biopolymer adsorption on the halloysite gyration radius. In addition, a morphological descript…

chemistry.chemical_classificationMaterials scienceNanostructureSupramolecular chemistryGeneral Physics and AstronomyFluorescence correlation spectroscopyHalloysite02 engineering and technologyPolymerengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesHalloysitePolyelectrolyte0104 chemical sciencesAdsorptionChemical engineeringchemistryengineeringBiopolymerPhysical and Theoretical Chemistry0210 nano-technology
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Dicyanobenzothiadiazole Derivatives Possessing Switchable Dielectric Permittivities

2017

Benzothiadiazoles are important electron acceptors and are frequently employed as electron-deficient components of donor-acceptor polymers. We report the effect of nitrile functionalities on the reactivity, steric hindrance, optoelectronic properties, and dielectric permittivity in dicyanobenzothioadiazole (DCNBT). Dielectric spectroscopy in the bulk and in solution assisted by DFT-calculations revealed that these molecules can be engineered to engender maximum values of the dipole moment and of dielectric permittivity due to the strong electron-withdrawing effect of the nitrile groups. The self-assembly in the bulk was investigated by X-ray scattering performed on single crystals, fibers (…

chemistry.chemical_classificationMaterials scienceNitrileRelative permittivity02 engineering and technologyPolymerDielectric010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesDielectric spectroscopyDipolechemistry.chemical_compoundchemistryChemical physicsLiquid crystalPhase (matter)Organic chemistryGeneral Materials Science0210 nano-technologyACS Applied Materials & Interfaces
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Dielectric study of orientational disorder in (CO2)1−x(N2O)xmixed crystals

1990

The dipolar relaxation dynamics of solid solutions of carbon dioxide and nitrous oxide has been investigated using dielectric spectroscopy. The temperature dependence of the relaxation rate reveals an ideal Arrhenius behavior for all concentrations, with energy barriers which scale linearly between the two pure compounds. The attempt frequencies are anomalously high. The distribution of relaxation times due to the static random fields as introduced by the substitutional impurity molecules is almost negligible. The melting temperature is determined by a critical relaxation rate of 40 kHz.

chemistry.chemical_classificationMaterials scienceNuclear magnetic resonancechemistryCondensed matter physicsImpurityRelaxation (physics)Dielectric lossDielectricInorganic compoundSolid solutionCole–Cole equationDielectric spectroscopyPhysical Review B
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