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Radioactive uranium

Ernest Rutherford observed that the paths taken by energetic particles emitted by radioactive uranium and thorium responded in three ways to magnetic fields slightly bent, strongly bent, and unaffected. He gave them the designations or, fi, and y. Even though scientists soon identified the particles, they still use these names to emphasize that they are nuclear decay products. [Pg.1566]

The best sealed-in minerals are zircons, zirconium silicate minerals which are formed when melted lava on the flanks of volcanoes solidifies. When the zircons crystallize out, they incorporate radioactive uranium (in particular 238U), which decays in several steps, leading Anally to the lead isotope 208Pb. The rate of decay is very low, as the half-life of uranium-238 is 4.5 x 109 years. Thus, the U-Pb-zircon method for age determination of Precambrian rock is very important. The fossils studied by Schopf were sandwiched between two lava layers (Schopf, 1999). The volcanic layers were dated to 3.458 0.0019 x 109 years and 3.471 0.005 x 109 years the age of the fossil layer (Apex chert) was thus determined to be about 3.465xlO9 years. [Pg.260]

Promethium is not found in nature. Therefore, it is by far the least abundant on Earth none exists on the Earth. AH of it is man-made in nuclear reactors. It is found only in the transmuted decay by-products ( ashes ) from the fission of radioactive uranium. [Pg.286]

The previous four chapters deal with the fractionation of stable trace elements during partial melting. In this chapter, we study the behaviors of radioactive uranium decay series during partial melting. Since quantitative models for uranium-series disequilibria need to include additional parameters in decay constants and are thus more complicated, for simplicity, we assume that the partition coefficients remain constant during partial melting. Thus, we only present modal dynamic melting. [Pg.74]

Joseph Lockyer (1836-1920) was one of the pioneers of solar spectroscopy. In examining the spectra of solar prominences in 1869, Lockyer noticed an absorption line that he could not identify. Reasoning that it represented an element not present on Earth, he proposed a new element - helium, from the Greek word helios for Sun. This idea failed to achieve acceptance from Lockyer s scientific colleagues until a gas having the same mysterious spectral line was found 25 years later in rocks. The helium in terrestrial uranium ore formed as a decay product of radioactive uranium. Thus, this abundant element was first discovered in the Sun, rather than in the laboratory. Lockyer s cosmochemical discovery was recognized by the British government, which created a solar physics laboratory for him. Lockyer also founded the scientific journal Nature, which he edited for 50 years. [Pg.9]

E. Kayser and H. Delaval observed that the presence of a radioactive uranium mineral increased the activity of nitrogen-fixing bacteria. A. W. Bosworth and co-workers observed that ammonia is produced by the human tubercle bacillus. [Pg.360]

One may rightfully raise the question as to why some products of nuclear reactions are radioactive while others are not. The answer concerns the stability of atomic nuclei. Essentially, any radioactive element, whether artificial or natural, can be considered abnormal. A nucleus that undergoes radioactive decay is in an unstable condition, and the process of decay always leads to stable isotopes. This tendency toward the achievement of stability is illustrated by the stepwise decay of naturally radioactive uranium to form a stable isotope of lead and the formation of stable carbon by the decay of artificial radioactive nitrogen. Although the conditions resulting in the instability of atomic nuclei are fairly well understood, further consideration of these factors is beyond the scope of this discussion. [Pg.637]

The fake Vermeers were eventually dated to the 1930s and 40s by Bernard Keisch at the Brookhaven National Laboratories in 1968. He analysed the radioactivity in the paintings and showed that the lead white that van Meegeren had used was relatively new. Lead contains a little radioactive uranium-238 which disintegrates through a series of... [Pg.202]

Appendix C contains the chemical formulae for the minerals used in this book. There are very few minerals that have the ideal crystalline structures discussed above. There are sufficient substitutional impurities, crystal defects, and distortions that make the CBPC structure significantly different from the models discussed above. Several well-established minerals exhibit these features, as are many of those listed in Appendix C. For example, Ca(UO2)2(PO4)2T0H2O is formed by the substitution of Ca in autunite by uranyl (UO2) ions, making the autunite a mineral of radioactive uranium. Similarly, (Ce,Th)P04 is formed by the substitution of the Ce in monazite by Th. Numerous minerals can be formed by substitutions and provide a researcher sufficient degree of freedom to synthesize very complex minerals to produce useful CBPCs. [Pg.94]

Because natural uranium produces very little radioactivity per mass of uranium, the renal and respiratory effects from exposure of humans and animals to uranium are usually attributed to the chemical properties of uranium. However, in exposures to more radioactive uranium isotopes (e.g., and and naturally occurring and U), it has been suggested that the chemical and radiological toxicity may be additive or may potentiate in some instances. In these instances, this dual mode of uranium toxicity may not be distinguishable by end point because of the overlap of etiology and manifested effects. The mechanism of this interaction is as yet unclear. [Pg.37]

A sample of radioactive uranium-containing ore exposes photographic film. [Pg.806]

A puzzling observation that led to the discovery of isotopes was the fact that lead obtained from uranium-containing ores had an atomic mass lower by two full atomic mass units than lead obtained from thorium-containing ores. Explain this result, using the fact that decay of radioactive uranium and thorium to stable lead occurs via alpha and beta emission. [Pg.821]

U-235. The chemistry of these isotopes, which is identical, determines the reactions of the isotopes within the environment as well as their transport and reactions within the body. All the isotopes of uranium emit primarily a particles. The U-238 isotope is the longest lived with a half-life of 4.5 billon years and constitutes more than 99% of the mass of natural uranium and half of its radioactivity. Uranium-234, a decay product of U-238, is responsible for nearly all the remainder of the radioactivity of natural uranium. A small amount (0.7% by weight) of fissionable U-235 is present in natural uranium. [Pg.2798]

Radioactive uranium-238 decays spontaneously in a long series of steps, the first of which is an alpha decay. When an alpha particle is emitted from a nucleus of uranium-238, the uranium atom loses two protons and two neutrons. The loss of protons makes the product another element, thorium, as shown in the following equation and in Figure 21.4. [Pg.747]

Well, you think that there may be another process which accounts for that. For example, suppose that a neutron is simply captured by a uranium atom and that the uranium then does not break apart. This process was in fact already known, and the resulting radioactive uranium was found on the piece of paper. But there was also another radioactivity with a different decay period that was not previously known, and that I suspected might belong to a new element, produced by the decay of the radioactive uranium. [Pg.132]

If we take a sample of pitchblende, which contains radioactive uranium, we can measure the amount of uranium and the amount of the ultimate decay product, lead. From the ratio of lead to uranium we can determine the age of the ore and from this information we can deduce the age of the earth. [Pg.217]

There have been two major accidents (Three Mile Island in the United States and Chernobyl in the former Soviet Union) in which control was lost in nuclear power plants, with subsequent rapid increases in fission rates that resulted in steam explosions and releases of radioactivity. The protective shield of reinforced concrete, which surrounded the Three Mile Island Reactor, prevented release of any radioactivity into the environment. In the Russian accident there had been no containment shield, and, when the steam explosion occurred, fission products plus uranium were released to the environment—in the immediate vicinity and then carried over the Northern Hemisphere, in particular over large areas of Eastern Europe. Much was learned from these accidents and the new generations of reactors are being built to be passive safe. In such passive reactors, when the power level increases toward an unsafe level, the reactor turns off automatically to prevent the high-energy release that would cause the explosive release of radioactivity. Such a design is assumed to remove a major factor of safety concern in reactor operation, see also Bohr, Niels Fermi, Enrico AIan-HATTAN Project Plutonium Radioactivity Uranium. [Pg.871]

The greatest health risk from large intakes of uranium is toxic damage to the kidneys, because, in addition to being weakly radioactive, uranium is a toxic metal. Uranium expo.sure also increases your risk of getting cancer due to its radioactivity. Since uranium tends to concentrate in specific locations iti the body, risk of cancer of the bone, liver cancer, and blood diseases (such as leukemia) are increased. Inhaled uranium increases the risk of lung cancer. [Pg.274]

In this type of extraction, micellar structures are retained by correctly selecting the ultrafiltration (UF) membrane (Scamehorn et al., 1988). Hydrophobic species are solubilized within the micelles, but surfactant monomers in equilibrium with the micelles can penetrate the membrane along with the free solutes in equilibrium with those solubilized in the micelles. Whereas several uses for this technique have been suggested, such as the collection of radioactive uranium and plutonium present in acid wastes during nuclear plant decommissioning, from our point of view its principal use is in enantiomeric separation (Overdevest et al., 1998). [Pg.601]

See also Activation Anaiysis Neutron Activation. Radio-chemicai Methods Natural and Artificial Radioactivity Uranium Radiotracers Radio-Reagent Methods Gamma-Ray Spectrometry. [Pg.4117]

The main passive techniques for locating the particles are based on the natural radiation (alpha, beta, and gamma) emitted from the radioactive uranium nuclei and then-progeny. Devices that are sensitive to radiation, like old-fashioned photographic films or their modern electronic equivalent (Fuji plate), have the advantage of size (large samples with many particles can be measured simultaneously) but their sensitivity is low so that long exposure times are required. [Pg.273]

Through his experiments with radioactive uranium in 1911, Rutherford described a nuclear model. By bombarding particles through thin gold foil, he predicted that atoms had positive cores that were much smaller than the rest of the atom. [Pg.76]

Radioactive decay seems to be a mathematical process. Experimenters have found that protons have the magic numbers of 2, 8, 20, 28, 50, 82, and 114. Neutrons have the same magic numbers as protons, plus the number 126. Radioactive uranium ( U) decays eventually to lead ( Pb). [Pg.153]

Other short-lived isotopes can, however, still be detected in nature. The element number 86, radon (Rn), has several isotopes, the most long-lived of which has a half-life of only 3.8 days. How is it then possible that we have radon problems in our mines and our houses The answer is that radon certainly disintegrates rapidly but is also being formed continuously. Radon is part of the radioactive uranium decay series ... [Pg.1174]

Significant health hazards have resulted from exposure to radioisotopes in the mining of uranium used as nuclear reactor fuel. The main hazards are from inhalation of radioactive uranium decay products. The most significant of these are radium-226 and radon-226. The radium is carried by dust... [Pg.501]

General. Emphasized in this section are sulfide ore bodies and natural solutions which are normally not radioactive. Uranium deposits are not included because they generally do not contain common lead and few data are yet available on other sorts of deposits, such as iron ore and gold. The bearing of lead isotopes on genesis of sulfide ore bodies is considered. [Pg.69]


See other pages where Radioactive uranium is mentioned: [Pg.784]    [Pg.412]    [Pg.387]    [Pg.329]    [Pg.184]    [Pg.199]    [Pg.318]    [Pg.343]    [Pg.300]    [Pg.689]    [Pg.681]    [Pg.106]    [Pg.107]    [Pg.447]    [Pg.729]    [Pg.31]    [Pg.175]    [Pg.27]    [Pg.47]    [Pg.564]    [Pg.669]   
See also in sourсe #XX -- [ Pg.260 ]

See also in sourсe #XX -- [ Pg.84 ]




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Depleted uranium radioactivity

Radioactive isotopes uranium/thorium decay series

Radioactive material, excepted package, articles manufactured from depleted uranium

Radioactive material, excepted package, articles manufactured from natural uranium

Radioactive materials uranium

Radioactive series, actinium uranium

Radioactivity of uranium

Radioactivity uranium-thorium

Radioactivity uranium/lead dating

Tailings from uranium mills radioactivity

Uranium mills radioactivity

Uranium mines, radioactivity

Uranium natural radioactive decay series

Uranium radioactive decay series

Uranium radioactive elements

Uranium radioactive isotopes

Uranium radioactivity

Uranium radioactivity

Uranium refineries radioactivity

Uranium, continued radioactivity

Uranium-235, radioactive decay

Uranium: atomic number radioactive decay

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