17 resultados para RADIOACTIVE WASTES


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In 1965-1966 R/V Mikhail Lomonosov conducted studies on concentrations of artificial radioactive products in the Northeast Atlantic. Concentration of strontium-90 at the end of 1965 and the beginning of 1966 was higher than the average level for the ocean and reached about 53 dpm/100 l in the surface layer. The most intense transport of artificial radioactive products out of the Irish Sea was detected in the northern and northeastern directions along the Hebrides and the Orkneys. In addition to radioactive fission products from nuclear weapons tests, radioactive wastes of atomic industrial facilities discharged into the ocean are an important source of radioactive contamination of some regions of the world ocean.

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During an expedition aboard R/V Pavel Gordienko (September, 2002) investigations in the Sea of Japan areas, where radioactive wastes were disposed by the former Soviet Union, were carried out in order to assess present level of radioactive contamination of marine environment. Concentration of I37Cs, radioecologically one of the most important radionuclides, in near-bottom sea water and bottom sediments were measured to be low, 2.8-17.2 Bq/m**3 and 3.2-27.2 Bq/kg dry weight, respectively, that did not differ significantly from levels elsewhere in the northwest Pacific Ocean arising from global fallout. Results of measurements were compared with results of the Joint Japanese- Korean -Russian expedition to the Sea of Japan in 1994.

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Gamma-spectrometric analysis was used for six sediment cores from the area occupied by metalliferous sediments in the Southeast Pacific. In five of these cores vertical distribution curves of 230Th enabled positions of equilibrium points to be determined and sediments to be dated. The ionium curve was normalized for one core. Vertical distribution of 230Th in metalliferous sediments resembles its distribution in normal ocean-floor sediments beyond the area of influence of active ridges. Sedimentation rates lay within the range 0.7-12.3 mm/ky.

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The main stages of the sedimentary cycle of uranium in modern marine basins are under consideration in the book. Annually about 18 thousand tons of dissolved and suspended uranium enters the ocean with river runoff. Depending on a type of a marine basin uranium accumulated either in sediments of deep-sea basins, or in sediments of continental shelves and slopes. In the surface layer of marine sediments hydrogenic uranium is predominantly bound with organic matter, and in ocean sediments also with iron, manganese and phosphorus. In diagenetic processes there occurs partial redistribution of uranium in sediments, as well as its concentration in iron-manganese, phosphate and carbonate nodules and biogenic phosphate detritus. Concentration of uranium in marine sediments of various types depending on their composition, as well as on forms of its entering, degree of differentiation and of sedimentation rates, on hydrochemical regime and water circulation, and on intensity of diagenetic processes.

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A description is given of a gamma-ray spectrometer complex consisting of four interchangeable, low-background NaI(Tl) crystals that operate simultaneously. The system is used in determination of concentrations of natural radioactive elements and sedimentation rates of bottom sediments by the ionium method. Three detector sizes are used, depending on amount of material available: 80x80; 100x100, and 150x150. The system is operated clockwise and data are brought out on a punch tape; results are computer-processed. Examples are shown of the complex use in determining sedimentation rates of bottom sediments in the Southeast Pacific and concentrations of natural radioactive elements in DSDP Hole 381.