Plutonium environment

Plutonium (Pu) is an artificial element of atomic number 94 that has its main radioactive isotopes at 2 °Pu and Pu. The major sources of this element arise from the manufacture and detonation of nuclear weapons and from nuclear reactors. The fallout from detonations and discharges of nuclear waste are the major sources of plutonium contamination of the environment, where it is trapped in soils and plant or animal life. Since the contamination levels are generally very low, a sensitive technique is needed to estimate its concentration. However, not only the total amount can be estimated. Measurement of the isotope ratio provides information about its likely... [Pg.369]

The corrosion behavior of plutonium metal has been summarized (60,61). a-Plutonium oxidizes very slowly in dry air, typically <10 mm/yr. The rate is accelerated by water vapor. Thus, a bright metal surface tarnishes rapidly in normal environments and a powdery surface soon forms. Eventually green PUO2 [12059-95-9] covers the surface. Plutonium is similar to uranium with respect to corrosion characteristics. The stabilization of 5-Pu confers substantial corrosion resistance to Pu in the same way that stabilization of y-U yields a more corrosion-resistant metal. The reaction of Pu metal with Hquid water produces both oxides and oxide-hydrides (62). The reaction with water vapor above 100°C also produces oxides and hydride (63). [Pg.196]

Mixed oxide fuel is not appropriate for all nuclear reactors. Plutonium requires faster neutrons in order to operate in a sustained chain reaction. Light-water reactors operate in a highly moderated environment. [Pg.870]

Other reasons for investigating plutonium photochemistry in the mid-seventies included the widely known uranyl photochemistry and the similarities of the actinyl species, the exciting possibilities of isotope separation or enrichment, the potential for chemical separation or interference in separation processes for nuclear fuel reprocessing, the possible photoredox effects on plutonium in the environment, and the desire to expand the fundamental knowledge of plutonium chemistry. [Pg.263]

The large and widespread production of plutonium in nuclear power stations combined with its high radiotoxicity has caused great public concern about "plutonium poisoning". Consequently, the spread of plutonium in the environment has been extensively studied for several decades. The results have been reported in journals and more recently in a number of monographs and conference proceedings (e.g. L- 7). ... [Pg.275]

All plutonium produced must be prevented from spreading into the environment. It is presently believed that the safest way is to store plutonium waste in deep underground facilities, and several such are now being constructed (8, 9, 12, 13). In the future, however, releases of various sizes must be anticipated, considering the large amounts of plutonium being handled. The hazards associated with such releases must be reliably assessed. [Pg.276]

Table I summarizes some typical distribution coefficients. Sediments become enriched in plutonium with respect to water, usually with a factor of vlO5. Also living organisms enrich plutonium from natural waters, but usually less than sediments a factor of 103 - 101 is common. This indicates that the Kd-value for sediment (and soil) is probably governed by surface sorption phenomena. From the simplest organisms (plankton and plants) to man there is clear evidence of metabolic discrimination against transfer of plutonium. In general, the higher the species is on the trophic level, the smaller is the Kd-value. One may deduce from the Table that the concentration of plutonium accumulated in man in equilibrium with the environment, will not exceed the concentration of plutonium in the ground water, independent of the mode of ingestion.

Research into the aquatic chemistry of plutonium has produced information showing how this radioelement is mobilized and transported in the environment. Field studies revealed that the sorption of plutonium onto sediments is an equilibrium process which influences the concentration in natural waters. This equilibrium process is modified by the oxidation state of the soluble plutonium and by the presence of dissolved organic carbon (DOC). Higher concentrations of fallout plutonium in natural waters are associated with higher DOC. Laboratory experiments confirm the correlation. In waters low in DOC oxidized plutonium, Pu(V), is the dominant oxidation state while reduced plutonium, Pu(III+IV), is more prevalent where high concentrations of DOC exist. Laboratory and field experiments have provided some information on the possible chemical processes which lead to changes in the oxidation state of plutonium and to its complexation by natural ligands. [Pg.296]

The major source of plutonium in natural waters is the atmospheric fallout from nuclear weapons tests. Fallout plutonium is ubiquitous in marine and freshwater environments of the world with higher concentrations in the northern hemisphere where the bulk of nuclear weapons testing occurred(3). Much of the research on the aquatic chemistry of plutonium takes place in marine and freshwater systems where only fallout is present. [Pg.297]

A second source of plutonium, dispersed more locally, is liquid effluent from fuel reprocessing facilities. One such is the fuel reprocessing plant at Windscale, Cumbria in the United Kingdom where liquid waste is released to the Irish Sea(6). Chemical analysis of this effluent shows that about one percent or less of the plutonium is in an oxidized form before it contacts the marine water(7). Approximately 95 percent of the plutonium rapidly adsorbs to particulate matter after discharge and deposits on the seabed while 5 percent is removed from the area as a soluble component ). Because this source provided concentrations that were readily detected, pioneering field research into plutonium oxidation states in the marine environment was conducted at this location. [Pg.297]

These various broad research observations generated questions about the influence of chemical environments in aquatic systems upon plutonium and what chemical species might be present. The oxidation states of plutonium, its associations with DOC, and its complexation by inorganic ions all seemed interrelated and important to the understanding of environmental transport. [Pg.301]

The mechanisms by which Pu(IV) is oxidized in aquatic environments is not entirely clear. At Oak Ridge, laboratory experiments have shown that oxidation occurs when small volumes of unhydrolyzed Pu(IV) species (i.e., Pu(IV) in strong acid solution as a citric acid complex or in 45 percent Na2Coj) are added to large volumes of neutral-to-alkaline solutions(23). In repeated experiments, the ratios of oxidized to reduced species were not reproducible after dilution/hydrolysis, nor did the ratios of the oxidation states come to any equilibrium concentrations after two months of observation. These results indicate that rapid oxidation probably occurs at some step in the hydrolysis of reduced plutonium, but that this oxidation was not experimentally controllable. The subsequent failure of the various experimental solutions to converge to similar high ratios of Pu(V+VI)/Pu(III+IV) demonstrated that the rate of oxidation is extremely slow after Pu(IV) hydrolysis reactions are complete. [Pg.303]

All of the information obtained in this research area depends upon indirect evidence through the use of nonisotopic carriers or normalized data in the form of ratios. These are subject to error but the trends and insights that have been obtained are very useful to the description of the behavior of plutonium in the environment. Better thermodynamic data in the range of environmental concentrations would be helpful in further quantification of chemical species, as would phenomenalogical descriptions of the behavior of plutonium in reasonably good models of the environment. [Pg.312]

Half-lives span a very wide range (Table 17.5). Consider strontium-90, for which the half-life is 28 a. This nuclide is present in nuclear fallout, the fine dust that settles from clouds of airborne particles after the explosion of a nuclear bomb, and may also be present in the accidental release of radioactive materials into the air. Because it is chemically very similar to calcium, strontium may accompany that element through the environment and become incorporated into bones once there, it continues to emit radiation for many years. About 10 half-lives (for strontium-90, 280 a) must pass before the activity of a sample has fallen to 1/1000 of its initial value. Iodine-131, which was released in the accidental fire at the Chernobyl nuclear power plant, has a half-life of only 8.05 d, but it accumulates in the thyroid gland. Several cases of thyroid cancer have been linked to iodine-131 exposure from the accident. Plutonium-239 has a half-life of 24 ka (24000 years). Consequently, very long term storage facilities are required for plutonium waste, and land contaminated with plutonium cannot be inhabited again for thousands of years without expensive remediation efforts. [Pg.832]

Officer CB, Lynch DR (1981) Dynamics of mixing in estuaries. Estuar Coast Shelf Sci 12 525-533 Olsen CR, Thein M, Larsen IL, Lowry PD, Mulholland PJ, Cutshall NH, Byrd JT, Windom HL (1989) Plutonium, 4 b, and caibon isotopes in the Savatmah Estuary - Riverbome versus marine sources. Environ Sci Technol 23 1475-1481... [Pg.604]

Bulman RA, Johnson TE, Ham GJ, et al. 1993. Speciation of plutonium in potato and the gastrointestinal transfer of plutonium and americium from potato. Sci Total Environ 129 267-289. [Pg.229]

Cataldo DA, Garland TR, Wildung RE. 1981. Foliar retention and leachability of submicron plutonium and americium particles. J Environ Qual 10(1) 31-37. [Pg.230]

Ham GJ, Harrison JD, Popplewell DS, et al. 1994. The gastrointestinal absorption of neptunium, plutonium and americium in a primate (C. jacchus). Sci Total Environ 145 1-6. [Pg.239]

Hamilton TF, Fowler SW, LaRosa J, et al. 1991. Comparative study of plutonium and americium bioaccumulation from two marine sediments contaminated in the natural environment. J Environ Radioact 14 211-223. [Pg.239]

Harrison JD, Naylor GPL, Stather JW. 1994. The gastrointestinal absorption of plutonium and americium in rats and guinea pigs after ingestion of dusts from the former nuclear weapons site at Maralinga Implications for human exposure. Sci Total Environ 143 211-220. [Pg.240]

Harrison JD, Smith H, David AF. 1988. Plutonium and americium uptake in rats fed with Cumbrian shellfish - implications for estimates of dose to man. Sci Total Environ 68 187-196. [Pg.240]

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Litaor MI. 1995. Spatial analysis of plutonium-239 + 240 and americium-241 in soils around Rocky Flats, Colorado. J Environ Qual 24 506-516. [Pg.246]

Livens FR, Horrill AD, Singleton DL. 1994. The relationship between concentrations of plutonium and americium in soil interstitial waters and their uptake by plants. Sci Total Environ 155 151-159. [Pg.247]

Markham OD, Puphal KW, Filer TD. 1978. Plutonium and americium contamination near a transuranic storage area in southeastern Idaho. J Environ Qual 7(3) 422-428. [Pg.249]

Naylor GPL, Haines JW, Whysall K, et al. 1993. Measurements of the gastrointestinal absorption and tissue distribution of plutonium, americium and polonium in experimental animals. Sci Total Environ 130 429-435. [Pg.252]

Nyhan JW, Drennon BJ, Abeele WV, et al. 1985. Distribution of plutonium and americium beneath a 33-yr old liquid waste disposal site. J Environ Qual 14(4) 501-509. [Pg.255]

Paatero J, Jaakkola T. 1998. Transfer of plutonium, americium and curium from fallout into reindeer after the Chernobyl accident. Boreal Environment Research 3 181-189. [Pg.255]

Penrose WR, Polzer WL, Essington EH, et al. 1990. Mobility of plutonium and americium through a shallow aquifer in a semiarid region. Environ Sci Technol 24(2) 228-234. [Pg.255]

Popplewell DS, Ham GJ, Johnson TE, et al. 1984. The uptake of plutonium-238, 239, 240, americium-241, strontium-90 and caesium-137 into potatoes. Sci Total Environ 38 173-181. [Pg.256]

Ryan TP, Dowdall AM, Long S, et al. 1999. Plutonium and americium in fish, shellfish and seaweed in the Irish environment and their contribution to dose. J Environ Radioact 44 349-369. [Pg.258]

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