Thorium-232, decay

By this time, the Periodic Table of elements was well developed, although it was considered a function of the atomic mass rather than atomic number. Before the discovery of radioactivity, it had been estabUshed that each natural element had a unique mass thus it was assumed that each element was made up of only one type of atom. Some of the radioactivities found in both the uranium and thorium decays had similar chemical properties, but because these had different half-Hves it was assumed that there were different elements. It became clear, however, that if all the different radioactivities from uranium and thorium were separate elements, there would be too many to fit into the Periodic Table. 

The uranium and thorium decay-series contain radioactive isotopes of many elements (in particular, U, Th, Pa, Ra and Rn). The varied geochemical properties of these elements cause nuclides within the chain to be fractionated in different geological environments, while the varied half-lives of the nuclides allows investigation of processes occurring on time scales from days to 10 years. U-series measurements have therefore revolutionized the Earth Sciences by offering some of the only quantitative constraints on time scales applicable to the physical processes that take place on the Earth. 

In this chapter we discuss improvements documented in the literature over the past decade in these areas and others. Chemical procedures, decay-counting spectroscopy, and mass spectrometric techniques published prior to 1992 were previously discussed by Lally (1992), Ivanovich and Murray (1992), and Chen et al. (1992). Because ICPMS methods were not discussed in preceding reviews and have become more commonly used in the past decade, we also include some theoretical discussion of ICPMS techniques and their variants. We also primarily focus our discussion of analytical developments on the longer-lived isotopes of uranium, thorium, protactinium, and radium in the uranium and thorium decay series, as these have been more widely applied in geochemistry and geochronology. 

Olley JM, Roberts RG, Murray AS (1997) A novel method for determining residence times of river and lake sediments based on disequilibriiun in the thorium decay series. Water Resom Res 33 1319-1326 Onac BP, Lauritzen S-E (1996) The climate of the last 150,000 years recorded in speleothems preliminary results from north-western Romania. Theor Appl Karstology 9 9-21 O Neil JR., Clayton RN, Mayeda TK (1969) Oxygen isotope fractionation in divalent metal carbonates. J ChemPhys 51 5547-5558... 

Moore WS (1992) Radionuclides of the uranium and thorium decay series in the estuarine enviromnent. In Uranium-series Disequilibrium Applications to Earth, Marine and Enviromnental Sciences. Ivanovich M, Harmon RS (eds) Clarendon Press, Oxford, p 396-422 Moore WS (1996) Large groundwater inputs to coastal waters revealed by Tla emichments. Nature 380 612-614... 

Soon after this discovery the harnessing of the technique to the measurement of all the U isotopes and all the Th isotopes with great precision immediately opened up the entire field of uranium and thorium decay chain studies. This area of study was formerly the poaching ground for radioactive measurements alone but now became part of the wonderful world of mass spectrometric measurements. (The same transformation took place for radiocarbon from the various radioactive counting schemes to accelerator mass spectrometry.)... 

In this volume, for the first time, all the methods for determining the uranium and thorium decay chain nuclides in Earth materials are discussed. The range of problems solvable with this approach is remarkable—a fitting, tribute to the Curies and the early workers who discovered them for us to use. 

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. ... 

Rn-220 is another isotope of radon and belongs to the thorium decay series. Due to its short half life of 55.6 s, reports on its concentrations in those gases and in natural water are still scant. They are also important for a better estimate of our exposure to natural radioactivity and also for the geochemical study of the forma tion of those radon isotopes and their underground movement. 

FIGURE 3.4. Isotopes of the uranium and thorium decay series. 

At present, there are no widely distributed certified reference materials containing all of the radionuclides in the uranium and thorium decay series. Such reference materials are needed to calibrate instruments that make radionuclide measurements and to compare analytical results from different laboratories. The most critical need is for reference materials in the 235U decay series 231Pa, 227Ac, and 223Ra. 

Two methods to secure very small samples of francium for examination use the decay processes of other radioactive elements. One is to bombard thorium with protons. The second is to start with radium in an accelerator, where, through a series of decay processes, the radium is converted to actinium, which in turn rapidly decays into thorium, and finally, thorium decays naturally into francium. Following is a schematic of the decay process used for the production of small amounts of Fr-223 which, in turn, after several more decay processes ends up as stable lead (Pb) ... 

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. 

The chemistry of neptunium (jjNp) is somewhat similar to that of uranium (gjU) and plutonium (g4Pu), which immediately precede and follow it in the actinide series on the periodic table. The discovery of neptunium provided a solution to a puzzle as to the missing decay products of the thorium decay series, in which all the elements have mass numbers evenly divisible by four the elements in the uranium series have mass numbers divisible by four with a remainder of two. The actinium series elements have mass numbers divisible by four with a remainder of three. It was not until the neptunium series was discovered that a decay series with a mass number divisible by four and a remainder of one was found. The neptunium decay series proceeds as follows, starting with the isotope plutonium-241 Pu-24l—> Am-24l Np-237 Pa-233 U-233 Th-229 Ra-225 Ac-225 Fr-221 At-217 Bi-213 Ti-209 Pb-209 Bi-209. 

When thorium emits alpha particles, it disintegrates into other daughter radionuclides (radioactive materials), such as radium-226 and radon-222 (from thorium-230 in the uranium-238 decay series) or radium-228 and thoron (radon-220 from thorium-232 in the thorium decay series). It eventually decays to stable lead-208 or -206, which is not radioactive. More information about the decay of thorium can be found in Chapter 3. The toxicological characteristics of radon, radium, and lead are the subject of separate ATSDR Toxicological profiles. 

Cochran JK. 1984. The fates of uranium and thorium decay series nuclides in the estuarine environment. Estuary Filter, 179-220. 

X 10 yr) and ends with stable ° Pb, after emission of eight alpha (a) and six beta (jS) particles. The thorium decay series begins with Th (ti/2 = 1.41 X 10 °yr) and ends with stable ° Pb, after emission of six alpha and four beta particles. Two isotopes of radium and Th are important tracer isotopes in the thorium decay chain. The actinium decay series begins with (ti/2 = 7.04 X 10 yr) and ends with stable Pb after emission of seven alpha and four beta particles. The actinium decay series includes important isotopes of actinium and protactinium. These primordial radionuclides, as products of continental weathering, enter the ocean primarily by the discharge of rivers. However, as we shall see, there are notable exceptions to this generality. 

Several organizations (e.g., NIST, NRC-Canada, and IAEA) provide sediment reference materials containing radionuclides, many of which are only certified for artificial radionuclides ( Cs, Sr, Am, and Pu). Certain specific radionuclides have no certified natural matrix materials, including ocean, lake, and river sediments. Although these sediments are certified for a few naturally occurring and artificial radionuclides, the extent of radioactive equilibrium of the uranium and thorium decay series in these environmental materials is not provided. NIST currently offers an ocean sediment Standard Reference Material (SRM 4357) in... 

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