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U-238 decay chain

Mr. Petr discussed the source term foimd in mining wastes, as a function of components of the U-238 decay chain and the relative equilibrium between U-238, Ra-226, and the contribution from the Th-232 series. Contaminated items (e.g., scrap metals) can be characterised by using approximate mass to surface specific activity ratios. [Pg.316]

Adsley, I, Backhouse, J.S., Nichols, A.L. and Toole, J. (1998). U-238 Decay Chain Resolution of Observed Anomalies in the Measured Secular Equilibrium Between Th-234 and Daughter Pa-234m, Appl. Radiat. Isotopes, 49, 1337-1344. [Pg.328]

Both decay chains involve a gaseous isotope. Rn-220 in the Th-232 decay chain is short-lived (<1 min) and is unlikely to diffuse from solids Rn-222 in the U-238 decay chain is longer-lived (3.8 d) and diffusion before daughters grow in is more credible. Short-lived daughters after the radon gap will exist for analytical purposes if their radon parents are present. It is noted that Pb-210 at the end of the U-238 chain is long-lived on the time scale of sample analysis (22 y), and will remain after sample collection even if Rn-222 is lost subsequently. [Pg.16]

Results for U-238 Decay Chain. Considering the U-238 chain, Pb-214 was chosen as the reference nuclide for the data review, since it is has the smallest number of results in the dataset below detection (7/1865). The Pb-214 results from all three labs are similar, although those from Lab 3 are typically higher than those from the other two labs and the difference is statistically significant. [Pg.16]

Empirically, a better fit is achieved by increasing the estimated p-emission from the Th-232 and U-238 decay chains by around x3.4. This is unphysical, equating to -10+13 decays, rather than the actual 4+6. The discrepancy is left unexplained here and the factor is treated simply as an empirical calibration term. In summary, there is an effective gross-P activity of around 0.9 Bq/g associated with these nuclides in materials from Dounreay. This is split approximately 0.7 Bq/g from K-40 and 0.2 Bq/g from Th-232 and U-238 daughters. It is less than the typical measured gross-p activity of 1.3 Bq/g (Labs 2 and 3)... [Pg.22]

One-sixteenth will remain after 4 half-lives, so 4 X 30 = 120 years. 71. Eight alpha particles and six beta particles are emitted in the decay chain from U-238 to Pb-206. (The numbers are the same for the alternate routes.)... [Pg.685]

Some of the neutrons released in the controlled chain reaction strike the nuclei of non-fissionable U-238 atoms. In this case, the U-238 captures the neutron and becomes a heavier uranium isotope, U-239, which eventually decays to produce plutonium-239. [Pg.156]

Transmutation-decay chains for U-238 and Th-232. (From Knief, R.A., Nuclear Engineering, Taylor Francis Group, Washington, DC, 1992. With permission.)... [Pg.701]

Reactor isotopic changes occur for two reasons irradiation effects (primarily due to fission and transmutation) and radioactive decay. Figure 21.5 shows the transmutation decay chains for U-238 and Th-232. [Pg.701]

Effect of Fuel Processing on Actinide Decay Chains. Chemical separation of thorium results in material containing Th-232 and Th-228 only. Secular equilibrium of Pb-212 and Bi-212 from Th-228 takes 40 days governed by the half-life of Ra-224. Secular equilibrium of Ac-228 takes around 50 years, governed by the half-life of Ra-228. Chemical separation of uranium results in material containing U-234, U-235 and U-238 only. Subsequent enrichment for fuel increases the proportions of U-235 and inevitably of U-234. Th-234 and Pa-234m achieve secular equilibrium with U-238 within a year, but... [Pg.15]


See other pages where U-238 decay chain is mentioned: [Pg.21]    [Pg.21]    [Pg.1289]    [Pg.571]    [Pg.314]    [Pg.686]    [Pg.686]    [Pg.2903]    [Pg.1018]    [Pg.20]    [Pg.92]    [Pg.330]    [Pg.1414]   
See also in sourсe #XX -- [ Pg.6 ]




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