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  • 2000-2004  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Water and environment journal 17 (2003), S. 0 
    ISSN: 1747-6593
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: A high microbiological quality of drinking water must be ensured to protect public health. The filtration techniques that are used in treating drinking water play an important role; however, a biofilm can form on granular-media filters and the accumulated bacteria can slough off and enter the filtered water.The aim of this research was to examine (a) the potential for biofilm formation and detachment from filter sand, and (b) the effect of different backwash regimes on biofilm removal. During the operation of the filter, bacteria became attached to the sand media, particularly in the top 30 mm of the filter bed. A water-only backwash at 20% and 40% bed expansion demonstrated poor removal of biofilm throughout the depth of the bed. Collapse-pulsing is a more efficient method and results in a reduction in the number of bacteria in the filtered water.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 107 (2000), S. 903-917 
    ISSN: 1435-1463
    Keywords: Keywords: Serotonin receptors ; β-adrenoceptors ; DOI ; pindolol ; locomotor activity ; rat.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary. [1] We have previously shown that the β-adrenergic/5-HT1 receptor partial agonist (−)-pindolol (2.0–32.0 μmol kg−1) enhances the increase in forward locomotion in rats produced by the 5-HT2 receptor agonist DOI (0.7 μmol kg−1) via net activation of post-synaptic 5-HT2 receptors. [2] It was found that neither the 5-HT1A receptor agonist and partial agonist, (±) 8-OH-DPAT (0.2–2.4 μmol kg−1) and (S)-(−)-UH-301, respectively, nor the 5-HT1A receptor antagonist WAY-100635 (0.09–1.5 μmol kg−1), substituted for (−)-pindolol in this in vivo behavioral model. [3] This also applies to the 5-HT1B receptor agonist and antagonist anpirtoline (0.3–4.0 μmol kg−1) and isamoltane (1.0–64.0 μmol kg−1), respectively. Neither of these compounds mimicked (−)-pindolol in its interactions with DOI. [4] The (−)-pindolol/DOI-induced increase in forward locomotion could be antagonized by the β1 adrenoceptor antagonist betaxolol (24 μmol kg−1). [5] It is suggested that the intrinsic efficacy of (−)-pindolol at β-adrenoceptors is an important aspect of its in vivo pharmacodynamic profile.
    Type of Medium: Electronic Resource
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