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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Radiation Applications & Instrumentation. Part 38 (1987), S. 263-267 
    ISSN: 0883-2889
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Radiation Applications & Instrumentation. Part 42 (1991), S. 389-393 
    ISSN: 0883-2889
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Letters B 277 (1992), S. 6-12 
    ISSN: 0370-2693
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 130 (1989), S. 399-407 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract A portable tritium sampler was developed for the stepwise collections of water vapour (HTO), hydrogen (HT) and hydrocarbons (CH3T) in the atmosphere. First, water vapour was collected in an electronic cooler and an HTO collection column containing 400 g of molecular sieve. Next, dried air was introduced into an HT collection column containing 150 g of palladium catalyst. Hydrogen was then converted to water by catalytic oxidation at room temperature and the resultant water was immediately adsorbed on the molecular sieve bed supporting the catalyst. The remaining gas was finally introduced into a CH3T collection column containing 100 g of molecular sieve through a platinum catalyst column, in which hydrocarbons were burnt at 400°C. The resultant water was adsorbed in the CH3T collection column. The collection efficiencies of water in the HTO, HT and CH3T collection columns were all estimated to be nearly 100%. This newly developed method was found to be useful for the routine tritium monitoring by applying it to actual air samples.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 239 (1999), S. 527-531 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Atmospheric tritium concentrations of tritiated water vapor (HTO), tritiated hydrogen (HT) and tritiated hydrocarbons (primarily tritiated methane, CH3T) have been measured in Fukuoka prefecture, Japan from 1984 to the present to establish a general database on the behavior of atmospheric tritium. HTO concentrations expressed in Bq/l-H2O vary within a range of 1.19 to 2.45, giving an overall average value of 1.86±0.077. HTO concentrations expressed in-mBq/m3-air vary within a range of 7.8 to 46.1 and have a strong correlation with the atmospheric humidity, being high in the summer and low in winter. In the case of HT and CH3T, no seasonal variations were observed with average monthly values of 23.1 to 61.0 mBq/m3-air and 8.3 to 23.9 mBq/m3-air, respectively. The present HTO concentrations are already close to the tritium level before nuclear testings. However, the present HT and CH3T concentrations are still higher by a factor of about 140 and 30, respectively, than those before the testings. Specific activities are estimated to be 14.6–16.7 TU for HTO, 5.5·105–1.0·106 TU for HT and 3.2·104–4·104 TU for CH3T. The apparent difference in the specific activities suggests a very slow transformation of these species in the atmosphere or a continuous supply of HT and CH3T with high specific activity. Residence time for atmospheric HT was found to be 6.5 years over the period 1988–92 and 10 years for 1988–95. These times are longer than 4.8 years given by Mason and Östlund in the 1970s, and thus indicate a supply to the atmosphere of HT from various tritium sources.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Stability and reproducibility of gel-suspension samples were investigated in order to evaluate the characteristic feature of the gel-suspension method for14C activity measurement. Commercially available gelling agent, N-lauroyl-L-glutamic-α,γ-dibutylamide, was used for the gelformatio of the samples. No change of the counting rate for the gel-suspension sample was observed for more than 2 years after the sample preparation. Four samples used for checking the reproducibility of the sample preparation method. The same values were obtained for the counting rate of14C activity within the counting error. No change of the counting rate was observed for the “re-gelated” sample. These results show that the gel-suspension method is appropriate for the14C activity measurement by the liquid scintillation method and is useful for a long-term preservation of the sample for repeated measurement.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Potted plants were exposed to D2O vapor in a greenhouse and uptake of D2O by leaf and deposition of D2O to pot soil were examined. Atmospheric D2O concentration in the greenhouse increased rapidly after starting the release and reached constant level in a few hours. Although the variation of D2O concentration in leaf followed that in air with showing a time delay, D2O concentration in leaf did not become the same level as that in air and vein showed lower concentration that lamina. D2O concentration in the pot soil increased slowly with diffusing in deeper layer.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 239 (1999), S. 523-526 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Surface seawater and water vapor about 10 m above the sea level were collected in the Pacific and Indian Oceans during the expedition of KH-96-5 to examine tritium concentrations in open sea. The tritium concentration in the water vapor was one order of magnitude higher than that in the surface seawater, attributed to downward movement of naturally occurring tritium from stratosphere to troposphere.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 243 (2000), S. 479-482 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Tritium concentrations were analyzed in organic and water fractions of fresh pine needles, dead and degraded pine needles accumulating on a pine forest floor to examine tritium cycle in a forest ecosystem. Tritium concentration was higher in the organic fraction of dead and degraded pine needles compared to others, suggesting two tritium sources. Rain is responsible for water fractions in the samples, while atmospheric hydrogen and methane are speculated to be responsible for high tritium level in the organic fraction of dead and degraded pine needles.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 242 (1999), S. 173-175 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Variation of tritium concentration was examined for 100 days in the course of degradation of fresh pine needles, which were left on a pine forest floor. No difference was observed on free water tritium (FWT) and organically bound tritium (OBT) concentrations of sterilized samples by gamma-ray irradiation or fumigation and control samples, attributable to incomplete sterilization. The OBT concentrations did not increase within the experimental period as the level of humus collected from the forest floor. The results suggest that a longer degradation time, more than 100 days, is necessary to elevate OBT up to the level, which is observed in the general environment.
    Type of Medium: Electronic Resource
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