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  • 1995-1999  (5)
  • 1996  (5)
  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Astrocytes exposed to hypoxia (H) or hypoxia/reoxygenation (H/R) maintain cell viability and display changes in protein biosynthesis. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of metabolically labeled astrocytes exposed to H showed induction of an ≈78-kDa polypeptide that demonstrated sequence identity with glucose-regulated protein (GRP) 78. Cell lysates from H/R astrocytes displayed induction of neuroprotective interleukin (IL) 6, which was present in a high-molecular-weight complex also containing GRP78, suggesting that GRP78 might be functioning as a chaperone during cellular stress consequent on H/R. Introduction of anti-sense oligonucleotide to GRP78 into astrocytes prevented expression of the protein and suppressed H/R-induced astrocyte release of IL-6 by ≈50%. These data indicate that modulation of astrocyte properties during oxygen deprivation results, in part, from intracellular glucose depletion and subsequent expression of GRP78, which sustains generation of neuroprotective IL-6 under the stress of H/R.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Amyloid-beta peptide is central to the pathology of Alzheimer's disease, because it is neurotoxic—directly by inducing oxidant stress, and indirectly by activating microglia. A specific cell-surface acceptor site that could focus its effects on target cells has been postulated but not ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 42 (1996), S. 135-137 
    ISSN: 1572-879X
    Keywords: Oxydehydrogenation ; propane ; propylene ; Mg-V-Sb-oxide catalyst ; reaction network
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Magnesium vanadates have been shown by various groups to be active oxydehydrogenation catalysts for the conversion of light paraffins to the corresponding olefins. The olefins produced have significant commercial value in petroleum and petrochemical industry. Recently, we reported that doping of the magnesium vanadates with antimony, antimony-phosphorus, or boron, produces catalysts with significantly better selectivities to olefins than those of the parent undoped catalysts. Among these, the composition Mg4V2SbOx was selected for further study of propane oxydehydrogenation and its reaction network. At 500°C and atmospheric pressure, the selectivity to propylene decreases monotonically from 75% to 5% as propane conversion is increased from 2% to 68%. An analysis of the reaction network reveals, that propylene is the only useful first formed product, that COx is produced largely by sequential oxidation of the in situ formed propylene, but also to a lesser extent direct from propane by a deep oxidation route. The presence of two parallel pathways for COx formation is of interest, as it suggests that partial and deep oxidations may occur at different surface sites or involve different forms of reactive oxygens. Both of these might be amenable to electronic modification by substitution or doping to achieve higher propylene selectivities and yields at higher propane conversions, or their catalytic behavior might be advantageously alterable through site isolation of the paraffin activation centers.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-879X
    Keywords: Oxydehydrogenation ; propane ; propylene ; Mg-V-Sb-oxide catalyst ; reaction kinetics ; mechanism ; site isolation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Recently we reported that Mg4V2Sb2Ox is selective for propane andn-butane Oxydehydrogenation at low hydrocarbon conversion, and that propane is oxidized in parallel reactions to propylene and COx. We report now on the kinetics of propane and propylene oxidations over this catalyst. The partial oxidations of propane and propylene and zero-order in oxygen, whereas deep oxidations of both hydrocarbons are half-order. This difference in reaction order indicates that different forms of reactive oxygen are involved in the partial and deep oxidation reactions. Presumably, nucleophilic lattice oxygen partakes in the partial oxidation, while electrophilic dissociatively adsorbed oxygen is involved in deep oxidation. A single activated surface adsorbed state of the hydrocarbons is thought to be involved in both the partial and deep oxidation reactions. An interpretation of the observed reaction kinetics in context of the Mg4V2Sb2Ox solid state chemistry, and the partial oxidation literature in general, suggests that selective oxydehydrogenation of propane occurs on isolated (Sb-O-V-O-Sb) sites, deep oxidation on multiple vicinal vanadium sites (Sb-O-V-O-V-O-Sb), and partial oxidation of propylene to acrolein on subsurface V-promoted antimony sites (Sb-O-Sb). Therefore, unproved selectivity of desired intermediates (propylene/acrolein) should be achieved by further lowering the vanadium concentration and/or through key solid state positioning of the vanadium in the catalyst lattice. Alternatively, selective doping to electronically decrease the electrophilicity of the waste forming sites and its appended oxygen should also help depress the waste forming reaction channels in favor of the desired partial oxidation channels. Finally it is anticipated that higher useful product yields would be attained with a compositionally optimized Mg-V-Sb-oxide catalyst by opting for a more stable, isolatable intermediate, e.g., acrylonitrile, by reacting propane in the presence of ammonia and oxygen (air) over this catalyst.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 59 (1996), S. 1365-1369 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermal stability of a series of organotellurium compounds was determined by thermogravimetric analysis and the stabilizing capacity of the most heat-resistant compounds assessed in natural rubber, polyethylene, and polypropylene by measurement of the oxidative induction time (OIT). The most active compounds, bis[4-(dimethylamino)phenyl]telluride (5) and bis[2,6-dimethyl-4-(dimethylamino)phenyl]telluride (10) stabilized natural rubber considerably at the 1% level and even more so at the 2% level. A similar stabilizing effect of compound 5 was found in polyethylene and polypropylene at the 0.1% level. © 1996 John Wiley & Sons, Inc.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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