The Distribution of Uranium and Thorium Decay‐Series Radionuclides in the Environment—A Review

放射性核素 沉积岩 地质学 地球化学 铀同位素 铀矿石 放射性衰变 同位素 放射性废物 矿物学 化学 核物理学 核化学 物理
作者
J.B. Cowart,William C. Burnett
出处
期刊:Journal of Environmental Quality [Wiley]
卷期号:23 (4): 651-662 被引量:126
标识
DOI:10.2134/jeq1994.00472425002300040005x
摘要

Abstract Natural radioactivity has played an indispensable role in the development of the earth to the form and shape that we now observe. Energy from radioactivity powers the large‐scale processes that move the continents and cycle the elements. Most of the energy due to radioactivity comes from members of the three decay‐series, two of which are parented by isotopes of uranium, 238 U and 235 U, and one by 232 Th. These decay‐series cascade to produce radioactive offspring such as Ra, Rn, and Po, but the ultimate fate of all members of these series is to end as a stable isotope of Pb. Rocks or minerals that provide sites for the long‐lived decay‐series parents, U and Th, are destined to be associated with the other members of the decay‐series. The rocks that tend to host U and Th include some crystalline rocks such as granite and quartz‐conglomerate metamorphics, and certain sedimentary rocks such as organic shales, sandstones, carbonates, and phosphorites. All materials at the earth's surface eventually are broken down to their constituent parts and then, usually by the agency of water, transported to environments where they again may be geochemically sorted. The sorting processes at or near the surface of the earth operate on radioelements just as they do on other elements. The result is that the various radioelements are not simply dispersed but rather tend to accumulate in certain environments or rock types. Thus, the behavior of the radioelements found in the natural environment is based on their geochemistry, half‐life, and the nature of their surroundings.
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