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  • Ag/Ce composite catalyst  (1)
  • 550 - Earth sciences
  • ASTROPHYSICS
  • Earthquake
  • Humans
  • 2005-2009
  • 1990-1994  (2)
  • 1994  (2)
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  • 2005-2009
  • 1990-1994  (2)
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  • 1
    ISSN: 1572-879X
    Keywords: Formaldehyde ; oxidative decomposition ; Ag/Ce composite catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Silver-cerium composite oxide was active for low temperature oxidative decomposition of formaldehyde. Its high activity was due partly to the high dispersion of active silver on the CeO2. The surface oxygen of this composite catalyst was removed more easily than those on single component Ag2O or CeC2, which also seemed to contribute to the high activity of this catalyst. IR analysis revealed that formaldehyde was decomposed both on silver-cerium composite catalyst and CeO2 in the presence of oxygen to produce methoxide, dioxymethylene, and/or polyoxymethylene even at room temperature. In addition bi-carbonate was formed on silver-cerium composite catalyst and formate was produced on CeO2. These intermediates suffered further oxidation at higher temperatures (373 and 423 K) easily on silver-cerium composite catalyst, whereas degradation of them was rather difficult on CeO2.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 1994-04-08
    Description: Although beta-amyloid is the main constituent of neurite plaques and may play a role in the pathophysiology of Alzheimer's disease, mechanisms by which soluble beta-amyloid might produce early symptoms such as memory loss before diffuse plaque deposition have not been implicated. Treatment of fibroblasts with beta-amyloid (10 nM) induced the same potassium channel dysfunction previously shown to occur specifically in fibroblasts from patients with Alzheimer's disease--namely, the absence of a 113-picosiemen potassium channel. A tetraethylammonium-induced increase of intracellular concentrations of calcium, [Ca2+]i, a response that depends on functional 113-picosiemen potassium channels, was also eliminated or markedly reduced by 10 nM beta-amyloid. Increased [Ca2+]i induced by high concentrations of extracellular potassium and 166-picosiemen potassium channels were unaffected by 10 nM beta-amyloid. In Alzheimer's disease, then, beta-amyloid might alter potassium channels and thus impair neuronal function to produce symptoms such as memory loss by a means other than plaque formation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Etcheberrigaray, R -- Ito, E -- Kim, C S -- Alkon, D L -- New York, N.Y. -- Science. 1994 Apr 8;264(5156):276-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Adaptive Systems, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8146663" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/*metabolism ; Amyloid beta-Peptides/*pharmacology ; Bombesin/pharmacology ; Calcium/metabolism ; Cell Line ; Cells, Cultured ; Dimethyl Sulfoxide/pharmacology ; Female ; Fibroblasts/*drug effects/metabolism ; Humans ; Male ; Phenotype ; Potassium Channel Blockers ; Potassium Channels/*drug effects/metabolism ; Potassium Chloride/pharmacology ; Solubility ; Tetraethylammonium ; Tetraethylammonium Compounds/pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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