Oxidative Atmosphere (oxidative + atmosphere)

Distribution by Scientific Domains


Selected Abstracts


Preparation, structure and photoluminescence properties of SiO2,coated ZnS nanowires

CRYSTAL RESEARCH AND TECHNOLOGY, Issue 10 2010
Changhyun Jin
Abstract It is essential to passivate one-dimensional (1D) nanostructures with insulating materials to avoid crosstalking as well as to protect them from contamination and oxidation. The structure and influence of thermal annealing on the photoluminescence properties of ZnS-core/SiO2 -shell nanowires synthesized by the thermal evaporation of ZnS powders followed by the sputter deposition of SiO2 were investigated. Transmission electron microscopy and X-ray diffraction analyses revealed that the cores and shells of the core-shell nanowires were single crystal zinc blende-type ZnO and amorphous SiO2, respectively. Photoluminescence (PL) measurement showed that the core-shell nanowires had a green emission band centered at around 525 nm with a shoulder at around 385 nm. The PL emission of the core-shell nanowires was enhanced in intensity by annealing in an oxidative atmosphere and further enhanced by subsequently annealing in a reducing atmosphere. Also the origin of the enhancement of the green emission by annealing is discussed based on the energy-dispersive X-ray spectroscopy analysis results. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


The Role of Oxidation in the Migration Mechanism of Layered Silicate in Poly(propylene) Nanocomposites

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 9 2006
Mauro Zammarano
Abstract Summary: Evidence of clay migration from the core to the surface of poly(propylene)/montmorillonite nanocomposites is provided. A three- to fivefold increase in the clay concentration of the surface is obtained during isothermal heating in oxidative atmosphere. The mechanism of migration is investigated by means of attenuated total reflectance Fourier transform infrared spectrometry. It is shown that oxygen plays a fundamental role in the migration mechanism. ,Si versus c for the annealed samples. [source]


Physical adsorption vs. chemical binding of undecylenic acid on porous silicon surface: a comparative study of differently functionalized materials

PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 7 2009
E. Pastor
Abstract To imply miscibility to porous silicon (PSi) used for biomedical purposes a number of functionalization methods are employed. In order to distinguish between a non-specific surfactant-like interaction (physical sorption) and chemical binding of unsaturated chemicals (undecylenic acid, UD) to H-terminated PSi surface we studied the two differently treated materials. Differential scanning calorimetry (DSC) and thermogravimetry (TGA), BET and FTIR measurements were performed with the PSi powder samples (n+ doped). Changes in surface area, weight loss, calorific effect and chemical composition that accompanied the thermal treatment have shown that the physisorbed UD molecules undergo a chemical process (binding) with the Si-Hx surface groups at about 150 °C in both, N2 inert atmosphere and in a synthetic air, oxidative atmosphere. Controlled conversion of physically sorbed molecules to the chemically attached ones is discussed with respect to methods of surface modification of PSi materials for increasing their biocompatibility. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Effect of intercalating agents on clay dispersion and thermal properties in polyethylene/montmorillonite nanocomposites

POLYMER ENGINEERING & SCIENCE, Issue 8 2008
Karen Stoeffler
Alkyl pyridinium, 1-vinyl alkyl imidazolium, 1,3-dialkyl imidazolium, and tetraalkyl phosphonium bromides were successfully used as intercalants for the preparation of highly thermally stable organophilic montmorillonites. Nanocomposites of linear low density polyethylene (LLDPE) and linear low density polyethylene grafted with maleic anhydride (LLDPE/LLDPE- g -MAH) were prepared from those organoclays. The micro- and nano-dispersions were analyzed through X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM): intercalation and/or partial exfoliation were found to occur only for formulations based on organoclays having an initial basal distance higher than 20 Å, suggesting the existence of a critical interfoliar distance for the delamination of silicate layers in a noninteracting polymer matrix. The properties of the nanocomposites were analyzed through differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and oscillatory rheometry. The dynamic crystallization of LLDPE was not significantly affected by the presence of clay. TGA in oxidative atmosphere proved to be very sensitive to the dispersion state of the organoclay: the thermal stability was drastically enhanced for intercalated and partially exfoliated formulations. However, the inherent thermal stability of the organoclay did not appear to influence significantly the overall thermal stability of the composite in the range of temperatures investigated (160,230°C). POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers. [source]


Kinetic analysis of thermo-oxidative degradation of PEEK/thermotropic liquid crystalline polymer blends

POLYMER ENGINEERING & SCIENCE, Issue 2 2006
M. Naffakh
The thermal degradation behavior of blends of poly(aryl ether ether ketone), PEEK, with a thermotropic liquid crystalline polymer (TLCP), Vectra®, were investigated in an oxidative atmosphere, using thermogravimetric analysis under dynamic conditions. The theoretical weight loss curves of the blends were compared with the experimental curves in order to explain the effect of blending on the thermal stability of the pure polymers. The thermo-oxidative degradation of PEEK/Vectra® blends of different compositions takes place in various steps and the characteristic degradation temperatures and the kinetic parameters such as activation energy are strongly influenced by blending. Polymer blends based on this TLCP polymer had not been previously studied from kinetic viewpoint. POLYM. ENG. SCI. 46:129,138, 2006. © 2005 Society of Plastics Engineers [source]


From the Linden Flower to Linden Honey , Volatile Constituents of Linden Nectar, the Extract of Bee-Stomach and Ripe Honey

CHEMISTRY & BIODIVERSITY, Issue 12 2004
Regula Naef
Honey is produced by honeybees (Apis mellifera), which collect nectar from flowers, digest it in their bodies, and deposit it in honeycombs, where it develops into ripe honey. We studied the evolution of the volatile constituents from the nectar of linden blossoms (Tilia cordata) to honey via the ,intermediate' honeybee. The sampling of the contents of the honey stomach or honey sack of the bee is unique. Extracts were prepared from nectar, from the liquid of the honey stomach, and from ripe honey. The chemistry is extremely complex, and compounds spanning from monoterpenes (hydrocarbons, ethers, aldehydes, acids, and bifunctional derivatives), isoprenoids, aromatic compounds (phenylpropanoids, phenols), and products degraded from fatty acids to alkaloids, were identified. Some compounds definitely stem from the plants, whereas other interesting constituents can be attributed to animal origin. Two derivatives of decanoic acid, 9-oxodec-2-enoic acid (12) and 9-hydroxydec-2-enoic acid, identified in the honey are known to be constituents of the so-called ,Queen's pheromone'. Two metabolites of these acids were identified in the extract of the honey stomach: 8-oxononanal (10), a new natural product, and 8-oxononanol (11). There structures were confirmed by synthesis. Nectar and honey stomach contain many aldehydes, which, due to the highly oxidative atmosphere in the honeycomb, are found as corresponding acids in the honey. Two acids were newly identified as 4-isopropenylcyclohexa-1,3-diene-1-carboxylic acid (14) and 4-(1-hydroxy-1-methylethyl)-cyclohexa-1,3-diene-1-carboxylic acid (15). [source]