Search results for "Plastics"

showing 10 items of 2724 documents

Capillary Imbibition, Crystallization, and Local Dynamics of Hyperbranched Poly(ethylene oxide) Confined to Nanoporous Alumina

2017

The crystallization and dynamics of hyperbranched poly(ethylene oxide) (hbPEO), obtained from the direct random copolymerization of EO and glycidol (PEO-co-PG), are studied both in bulk and within nanoporous alumina (AAO). Copolymerization decreases the degree of crystallinity and lowers the crystallization and melting temperatures as compared to linear PEO. The dynamics of capillary imbibition within AAO followed the t1/2 prediction but is slower than predicted by the classical Lucas–Washburn equation. The most prominent effect of confinement is the change in nucleation mechanism—from heterogeneous nucleation in bulk to homogeneous nucleation inside AAO. The homogeneous nucleation temperat…

Materials sciencePolymers and PlasticsEthylene oxideNanoporousOrganic ChemistryOxideNucleation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistryCrystallinitychemistry.chemical_compoundchemistryChemical engineeringlawPolymer chemistryMaterials ChemistryCopolymerImbibitionCrystallization0210 nano-technologyMacromolecules
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Thermodynamics of Phase Behavior in PEO/P(EO-b-DMS) Homopolymer and Block Co-Oligomer Mixtures under Pressure

2003

The cloud-point temperatures (T-cl's) of poly(ethylene oxide) (PEO) and poly(ethylene oxide)-block-polydimethylsiloxane (P(EO-b-DMS)) homopolymer and block-oligomer mixtures were determined by turbidity measurements over a range of temperatures (105 to 130degrees), pressures (1 to 800 bar), and compositions (10-40 wt.-% PEO). The system phase separates upon cooling and T-cl was found to decrease with an increase in pressure for a constant composition. In the absence of special effects, this finding indicates negative excess volumes. Special attention was paid to the demixing temperatures as a function of the pressure for the different polymer mixtures and the plots in the T-phi plane (where…

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryEnthalpyThermodynamicsFlory–Huggins solution theoryEntropy of mixingCondensed Matter Physicschemistry.chemical_compoundchemistryVolume (thermodynamics)Phase (matter)Polymer chemistryMaterials ChemistryPolymer blendPhysical and Theoretical ChemistryBar (unit)Macromolecular Chemistry and Physics
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Branched Acid-Degradable, Biocompatible Polyether Copolymers via Anionic Ring-Opening Polymerization Using an Epoxide Inimer

2022

The introduction of acid-degradable acetal moieties into a hyperbranched polyether backbone has been achieved by the design of a novel epoxide-based degradable inimer. This new monomer, namely, 1-(glycidyloxy)ethyl ethylene glycol ether (GEGE), has been copolymerized in the anionic ring-opening polymerization (AROP) with ethylene oxide (EO) or glycidol (G), respectively, yielding branched polyethers, that is, P(EO-co-GEGE) and P(G-co-GEGE), that possess an adjustable amount of acid-cleavable acetal units. In addition, a novel class of multiarm star copolymers P(G-co-GEGE-g-EO) with acid-labile polyether core and PEG side chains was synthesized by using the P(G-co-GEGE) copolymers as multifu…

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryGlycidolEpoxideRing-opening polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryEthylene glycolACS Macro Letters
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Hyperbranched PEG by Random Copolymerization of Ethylene Oxide and Glycidol

2010

The synthesis of hyperbranched poly(ethylene glycol) (hbPEG) in one step was realized by random copolymerization of ethylene oxide and glycidol, leading to a biocompatible, amorphous material with multiple hydroxyl functionalities. A series of copolymers with moderate polydispersity ($\overline {M} _{{\rm w}} /\overline {M} _{{\rm n}} $ < 1.8) was obtained with varying glycidol content (3-40 mol-%) and molecular weights up to 49 800 g mol(-1) . The randomly branched structure of the copolymers was confirmed by (1) H and (13) C NMR spectroscopy and thermal analysis (differential scanning calorimetry). MTS assay demonstrated low cell toxicity of the hyperbranched PEG, comparable to the highly…

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryGlycidolchemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymer chemistryContent (measure theory)PEG ratioMaterials ChemistryCopolymerThermal analysisEthylene glycolMacromolecular Rapid Communications
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The poly(propylene oxide-co-ethylene oxide) gradient is controlled by the polymerization method: determination of reactivity ratios by direct compari…

2019

An investigation of the highly relevant copolymerization of ethylene oxide (EO) and propylene oxide (PO) by in situ1H NMR spectroscopy shows striking differences in the copolymerization kinetics, depending on the polymerization method. Examination of the EO/PO copolymerization kinetics using iBu3Al for the monomer-activated anionic ring opening polymerization (AROP) confirmed a strong monomer gradient of the microstructure (rEO = 6.4, rPO = 0.16) in contrast to the known weak gradient in the conventional AROP (rEO = 2.8, rPO = 0.25). The first study via in situ1H-NMR kinetics of the copolymerization of PO and EO under heterogeneous double metal cyanide (DMC) catalysis, a method that produce…

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryKineticsBioengineering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryRing-opening polymerization0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationCopolymerPhysical chemistryReactivity (chemistry)Propylene oxide0210 nano-technologyPolymer Chemistry
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New amphiphilic poly(butadiene)-graft-poly(ethylene oxide)s

1995

Amphiphilic graft copolymers with a poly(butadiene) backbone and poly(ethylene oxide) side chains were synthesized by grafting isocyanateterminated poly(ethylene oxide) on to partially hydroxylated poly(butadiene). The graft copolymers are water soluble if the fraction of hydrophilic poly(ethylene oxide) exceeds 50 wt%. Solutions of graft copolymers in water and tetrahydrofuran were studied by static light scattering and viscosity measurements. By dynamic light scattering in solution it was shown that the graft copolymers form clusters.

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryOxidechemistry.chemical_compoundsurgical procedures operativePolybutadienechemistryDynamic light scatteringPolymer chemistryAmphiphileMaterials ChemistryCopolymerSide chainStatic light scatteringPolymer International
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Evidence of nickel ions dimerization in NiWO4 and NiWO4-ZnWO4 solid solutions probed by EXAFS spectroscopy and reverse Monte Carlo simulations

2021

Abstract The existence of exchange-coupled Ni 2 + ions – the so-called magnetic dimers – in wolframite-type NiWO 4 and Zn c Ni 1 − c WO 4 solid solutions with high nickel content was discovered by X-ray absorption spectroscopy combined with reverse Monte Carlo (RMC) simulations. Temperature- (10–300 K) and composition-dependent X-ray absorption spectra were measured at the Ni K-edge, Zn K-edge, and W L 3 -edge of microcrystalline NiWO 4 , Zn c Ni 1 − c WO 4 and ZnWO 4 . Structural models were obtained from simultaneous analysis of the extended X-ray absorption fine structure (EXAFS) spectra at three metal absorption edges using RMC simulations. The obtained radial distribution functions for…

Materials sciencePolymers and PlasticsExtended X-ray absorption fine structureAbsorption spectroscopyMetal ions in aqueous solutionMetals and AlloysAnalytical chemistry02 engineering and technologyReverse Monte CarloAtmospheric temperature range021001 nanoscience & nanotechnologyRadial distribution function01 natural sciencesElectronic Optical and Magnetic Materials0103 physical sciencesCeramics and CompositesAbsorption (chemistry)010306 general physics0210 nano-technologySolid solutionActa Materialia
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Temperature dependence of the local structure and lattice dynamics of wurtzite-type ZnO

2014

Temperature-dependent (10–300 K) Zn K-edge extended X-ray absorption fine structure (EXAFS) spectra of polycrystalline wurtzitetype ZnO were analyzed using ab initio multiple-scattering theory and taking into account anisotropy of the crystallographic structure and thermal disorder. We employed two different simulation approaches: classical molecular dynamics (MD) and reverse Monte Carlo coupled with an evolutionary algorithm (RMC/EA method). The accuracy of several force-field models, which are commonly used in the MD simulations of bulk and nanostructured ZnO, was tested based on a comparison between the experimental and simulated Zn K-edge EXAFS spectra. It was found that available force…

Materials sciencePolymers and PlasticsExtended X-ray absorption fine structureMetals and AlloysAb initio02 engineering and technologyReverse Monte CarloCrystal structure021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsElectronic Optical and Magnetic MaterialsMolecular dynamicsCrystallographyCondensed Matter::Materials Scienceddc:6700103 physical sciencesCeramics and CompositesWyckoff positions010306 general physics0210 nano-technologyAnisotropyWurtzite crystal structure
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Ab initio calculations of indium arsenide in the wurtzite phase: structural, electronic and optical properties

2013

Most III-V semiconductors, which acquire the zinc-blende phase as bulk materials, adopt the metastable wurtzite phase when grown in the form of nanowires. These are new semiconductors with new optical properties, in particular, a different electronic band gap when compared with that grown in the zinc-blende phase. The electronic gap of wurtzite InAs at the Gamma-point of the Brillouin zone (E0 gap) has been recently measured, E0 = 0.46 eV at low temperature. The electronic gap at the A point of the Brillouin zone (equivalent to the L point in the zinc-blende structure, E1) has also been obtained recently based on a resonant Raman scattering experiment. In this work, we calculate the band st…

Materials sciencePolymers and PlasticsFOS: Physical sciencesBiomaterialschemistry.chemical_compoundsymbols.namesakeCondensed Matter::Materials ScienceAb initio quantum chemistry methodsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Electronic band structureWurtzite crystal structureCondensed Matter - Materials ScienceCondensed matter physicsCondensed Matter - Mesoscale and Nanoscale PhysicsCondensed Matter::Otherbusiness.industryMetals and AlloysMaterials Science (cond-mat.mtrl-sci)Condensed Matter::Mesoscopic Systems and Quantum Hall EffectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBrillouin zoneSemiconductorchemistryCrystal field theorysymbolsIndium arsenidebusinessRaman scattering
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Coupling of Nanoparticle Dynamics to Polymer Center-of-Mass Motion in Semidilute Polymer Solutions

2017

We investigate the dynamics of nanoparticles in semidilute polymer solutions when the nanoparticles are comparably sized to the polymer coils using explicit- and implicit-solvent simulation methods. The nanoparticle dynamics are subdiffusive on short time scales before transitioning to diffusive motion on long time scales. The long-time diffusivities scale according to theoretical predictions based on full dynamic coupling to the polymer segmental relaxations. In agreement with our recent experiments, however, we observe that the nanoparticle subdiffusive exponents are significantly larger than predicted by the coupling theory over a broad range of polymer concentrations. We attribute this …

Materials sciencePolymers and PlasticsFOS: Physical sciencesMotion (geometry)Nanoparticle02 engineering and technologyCondensed Matter - Soft Condensed Matter010402 general chemistry01 natural sciencesInorganic ChemistryMaterials ChemistryDiffusion (business)Couplingchemistry.chemical_classificationQuantitative Biology::BiomoleculesRange (particle radiation)Organic ChemistryDynamics (mechanics)Polymer021001 nanoscience & nanotechnology0104 chemical sciencesCondensed Matter::Soft Condensed MatterchemistryChemical physicsSoft Condensed Matter (cond-mat.soft)Center of mass0210 nano-technologyMacromolecules
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