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  • 1
    ISSN: 1432-2072
    Keywords: Self-Infusion ; Primates ; Secobarbital ; Chlordiazepoxide ; Choice Procedure ; Preference ; Multiple Addiction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Monkeys were exposed to a 24 h continuous experimental procedure which provided a periodic forced choice between the self-infusion of secobarbital versus saline. Preference for secobarbital over saline was readily obtained using choice trials programmed approximately every 2 h at a dose of 9 mg/kg of secobarbital per infusion. Preference for self-infusion of chlordiazepoxide over saline was obtained using choice trials every 3 h, and a dose on the order of 1 mg/kg per infusion. In a subsequent experiment, two of the animals addicted to chlordiazepoxide were given a choice every 3 h between an infusion of chlordiazepoxide or secobarbital. Following a period of intake of both drugs, a gradual shift in preference from chlordiazepoxide to secobarbital was observed over a period of some 60 days. In general, this preference procedure provides a flexible technique with several dependent measures for single or multiple drug addiction studies.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 511-533 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The temperature dependence of x-ray small-angle scattering from fractionated linear polyethylene crystallized from the melt was determined experimentally over a range of temperatures from room temperature to the melting point. It was found in general that only the most intense of the several small-angle peaks exhibited a thermally dependent behavior. Below the crystallization temperature this peak increased in intensity with temperature, at constant peak position. Recrystallization was manifest in a discontinuous shift of the peak. During isothermal crystallization, the peak intensity first increased, then decreased, with time. It is concluded from supplementary electron microscopy and from the behavior of the peak that its position reflects the period of stacking of lamellae and that its intensity is controlled primarily by the thickness of the layer separating lamellae. The reversible peak intensity effect is attributed to an entropydriven growth of the interlamellar layer at the expense of the crystalline lamellae. The intensity effects observed during crystallization are associated with the primary and secondary phases of crystallization. Lamellar surface free energies were computed from melting point observations and were found to increase with molecular weight.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 7 (1985), S. 69-73 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Strong suppression of molecular ions in positive secondary ion mass spectra (SIMS) is achieved by electric isolation of a specimen (SI) with an electrically charged aperture situated immediately above its surface. This technique is also useful for controlling the surface charging on an insulator. The origin of this phenomenon has been explored using metals and semiconductors as models. The strong molecular suppression effect is found to result from the very high ion kinetic energies (〉400 eV) emerging from the surface under SI conditions. The charged aperture is believed to stabilize surface charging by confining it within a small region. SI methods for reducing molecular ions in silicon and mild steel specimens reduce major molecular fragments by 3-4 orders of magnitude.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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