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Thorium-234, radioactive decay

There is subterranean production of chlorine-36 and the world average chlorine contents of granite and basalt have been given as around 50 and 200 ppm, respectively. Sedimentary rocks have variable contents ranging from 10 ppm in sandstones to 20,000 ppm in deep-sea limestones. Rock outcrops are exposed to the cosmic neutron flux so that some chlorine-36 results from neutron capture by chlorine-35, but, below a few meters, it is ineffectual. Nonetheless, some chlorine-36 results from an in situ neutron flux in rock matrices caused by (a,n) reactions triggered by alpha particles from uranium and thorium radioactive decay systems. This flux may be of the order of 10 cm s (Kuhn et al. 1984). [Pg.772]

Lead occurs naturally as a mixture of four non-radioactive isotopes, and Pb, as well as the radioactive isotopes ° Pb and Pb. All but Pb arise by radioactive decay of uranium and thorium. Such decay products are known as radiogenic isotopes. [Pg.365]

Argon-40 [7440-37-1] is created by the decay of potassium-40. The various isotopes of radon, all having short half-Hves, are formed by the radioactive decay of radium, actinium, and thorium. Krypton and xenon are products of uranium and plutonium fission, and appreciable quantities of both are evolved during the reprocessing of spent fuel elements from nuclear reactors (qv) (see Radioactive tracers). [Pg.4]

The same chemical separation research was done on thorium ores, leading to the discovery of a completely different set of radioactivities. Although the chemists made fundamental distinctions among the radioactivities based on chemical properties, it was often simpler to distinguish the radiation by the rate at which the radioactivity decayed. For uranium and thorium the level of radioactivity was independent of time. For most of the radioactivities separated from these elements, however, the activity showed an observable decrease with time and it was found that the rate of decrease was characteristic of each radioactive species. Each species had a unique half-life, ie, the time during which the activity was reduced to half of its initial value. [Pg.443]

Polonium, completing the elements of Group 16, is radioactive and one of the rarest naturally occurring elements (about 3 x 10 " % of the Earth s crust). The main natural source of polonium is uranium ores, which contain about lO g of Po per ton. The isotope 210-Po, occurring in uranium (and also thorium) minerals as an intermediate in the radioactive decay series, was discovered by M. S. Curie in 1898. [Pg.4]

As early as 1902, Rutherford and his colleague, the chemist Frederick Soddy, realized that emissions of alpha and beta rays changed the nature of the emitting substance. One example of such a change is the spontaneous radioactive decay of the uranium-238 isotope, which emits an alpha particle and produces thorium ... [Pg.36]

The equations governing the age of secondary carbonate deposits stated above assume that all °Th or Pa present in the mineral is formed in situ by radioactive decay of co-precipitated U. Thorium and Pa content at time of formation can often be considered to be negligible in the pure authigenic phase of calcite or aragonite... [Pg.412]

Many scientists thought that Earth must have formed as long as 3.3 billion years ago, but their evidence was confusing and inconsistent. They knew that some of the lead on Earth was primordial, i.e., it dated from the time the planet formed. But they also understood that some lead had formed later from the radioactive decay of uranium and thorium. Different isotopes of uranium decay at different rates into two distinctive forms or isotopes of lead lead-206 and lead-207. In addition, radioactive thorium decays into lead-208. Thus, far from being static, the isotopic composition of lead on Earth was dynamic and constantly changing, and the various proportions of lead isotopes over hundreds of millions of years in different regions of the planet were keys to dating Earth s past. A comparison of the ratio of various lead isotopes in Earth s crust today with the ratio of lead isotopes in meteorites formed at the same time as the solar system would establish Earth s age. Early twentieth century physicists had worked out the equation for the planet s age, but they could not solve it because they did not know the isotopic composition of Earth s primordial lead. Once that number was measured, it could be inserted into the equation and blip, as Patterson put it, out would come the age of the Earth. ... [Pg.170]

Natural lead, a metallic element, is a mixture of the following four isotopes lead-204, lead-206, lead-207, and lead-208. Only lead-204 is a primordial isotope of nonradiogenic origin all the others are radiogenic, each isotope being the end product of one of the radioactive decay series of isotopes of thorium or uranium, namely, uranium-238, uranium-235, and thorium-232 the decay series of the uranium isotopes are listed in Figure 12 ... [Pg.158]

The four isotopes, as those of any element, have the same chemical properties. The four are not, however, uniformly distributed in the earth s crust the occurrence of three of them, in minerals and rocks, is associated with the radioactive decay of isotopes of thorium and uranium. In most minerals and rocks the relative amounts (or the isotopic ratios) of the isotopes of lead (often expressed relative to the amount of stable lead-204) are generally within well-known ranges, which are independent of the composition of the mineral or rock they are, however, directly related to the amounts of radioactive thorium and uranium isotope impurities in them. [Pg.158]

The rate constant for the radioactive decay of thorium-232 is 5.0 X 10 u/year. Determine the half-life of thorium-232. [Pg.193]

Radium, thorium, and other radionuclides accumulate in uranium mill tailings. The potential environmental effects of these radionuclides has become of increasing concern to the public. In the future, it may be necessary to modify existing uranium recovery processes to accommodate removal of radium and perhaps other radioactive decay products of uranium. [Pg.553]

Various radium isotopes are derived through a series of radioactive decay processes. For example, Ra-223 is derived from the decay of actinium. Ra-228 and Ra-224 are the result of the series of thorium decays, and Ra-226 is a result of the decay of the uranium series. [Pg.81]

ISOTOPES There are 41 isotopes of polonium. They range from Po-188 to Po-219. All of them are radioactive with half-lives ranging from a few milliseconds to 102 years, the latter for its most stable isotope Po-209. Polonium is involved with several radioactive decay series, including the actinium series, Po-211 and Po-215 the thorium series, Po-212 and Po-216 and the uranium decay series, Po-210, Po-214, and Po-218. [Pg.241]

While studying radium, Friedrich Ernst Dorn (1848—1916) found that it gave off a radioactive gas that, when studied in more detail, proved to be the sixth noble gas. Dorn was given credit for its discovery in 1900. He called it radon, a variation of the word radium. Sir Wdham Ramsay and R. W. Whytlaw-Gray, who also investigated the properties of radon, called it niton from the Latin word nitens, which means shining. Several other scientists who worked with radon named it thoron because of the transmutation of radon-220 from the decay of thorium. However, since 1923, the gas has been known as radon because it is the radioactive decay gas of the element radium. The name is derived from the Latin word radius, which means ray. ... [Pg.273]

As thorium undergoes natural radioactive decay, a number of products, including gases, are emitted. These decay products are extremely dangerous radioactive poisons if inhaled or ingested. [Pg.311]

Thorium occurs naturally primarily as the very long-lived Th (iii2> 10 years), along with small amounts of other isotopes resulting from the radioactive decay of and It is so weakly radioactive that very few precautions are necessary in its handling. [Pg.17]

Since transport by water is virtually the only available mechanism for escape, we will be predominantly concerned with the chemistry of aqueous solutions at the interface with inorganic solids - mainly oxides. These will be at ordinary to somewhat elevated temperatures, 20-200 C, because of the heating effects of radioactive decay during the first millennium. The elements primarily of interest (Table I) are the more persistent fission products which occur in various parts of the periodic table, and the actinides, particularly uranium and thorium and, most important of all, plutonium. [Pg.337]

French and Polish chemists Pierre and Marie Curie Named for Marie Curie s native Poland formed by the radioactive decay of uranium and thorium has the most identified isotopes of any element. [Pg.249]

French chemist Marguerite Perey Heavy, unstable, alkali metal produced by radioactive decay of uranium and thorium probably less than one ounce is present in the Earth s crust. [Pg.249]

In the environment, thorium and its compounds do not degrade or mineralize like many organic compounds, but instead speciate into different chemical compounds and form radioactive decay products. Analytical methods for the quantification of radioactive decay products, such as radium, radon, polonium and lead are available. However, the decay products of thorium are rarely analyzed in environmental samples. Since radon-220 (thoron, a decay product of thorium-232) is a gas, determination of thoron decay products in some environmental samples may be simpler, and their concentrations may be used as an indirect measure of the parent compound in the environment if a secular equilibrium is reached between thorium-232 and all its decay products. There are few analytical methods that will allow quantification of the speciation products formed as a result of environmental interactions of thorium (e.g., formation of complex). A knowledge of the environmental transformation processes of thorium and the compounds formed as a result is important in the understanding of their transport in environmental media. For example, in aquatic media, formation of soluble complexes will increase thorium mobility, whereas formation of insoluble species will enhance its incorporation into the sediment and limit its mobility. [Pg.122]

In 1900 Rutherford and the English chemist Frederick Soddy, working at McGill University in Montreal, showed that radioactive thorium emits atoms of the noble gas radon. Where did this inert element come from Rutherford and Soddy concluded that thorium was turning into a different element by undergoing radioactive decay. [Pg.95]

One of the most important observations of atoms is the set of relationships between elements that belong to one of the series of radioactive decays. The parent elements of uranium, thorium and actinium decay through many intermediates to the stable element lead. The Nobel Prize in Chemistry for 1921 was awarded in 1922 to Frederick Soddy for his complete characterization of these processes. The story is beautifully told in his Nobel Lecture entitled The origins of the conception of isotopes (25). [Pg.96]

The element lead is composed of four istotopes—208Pb, 207Pb, 206Pb, and 204Pb. The first three are the stable end products of the radioactive decay of uranium and thorium. [Pg.9]


See other pages where Thorium-234, radioactive decay is mentioned: [Pg.443]    [Pg.313]    [Pg.1254]    [Pg.443]    [Pg.366]    [Pg.57]    [Pg.57]    [Pg.305]    [Pg.192]    [Pg.237]    [Pg.464]    [Pg.6]    [Pg.13]    [Pg.305]    [Pg.442]    [Pg.12]    [Pg.165]    [Pg.123]    [Pg.123]    [Pg.11]    [Pg.59]    [Pg.460]    [Pg.400]    [Pg.458]   
See also in sourсe #XX -- [ Pg.552 ]




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