MadSci Network: Other |
I am going to give a general answer to this one, rather than historical detail. The latter can be found in reference books. Radioactive half-lives can be determined in several different ways. It depends mainly on which particular half-life is under consideration. There is an enormous range in the actual time-scale of radioactive decay -- from fractions of a second through to a million times the age of the earth! For half lives in the region of an hour or two to a year or two, the problem is very readily solved: you simply get your radioactive source, and follow the decrease in its decay rate by checking it from time to time with a geiger counter. For shorter half-lives, you must again obtain your data by simply following the decreasing decay rate. But this involves electronic counting with much more sophisticated equipment. Generally speaking, isotopes with very short half lives were produced and investigated much later than those with medium or very long half-lives. For long half-lives, the approach must be quite a different one. U-238 (the dominant isotope of natural uranium) has a half life of about 4 billion years; one could not simply get hold of a uranium sample and wait for its radioactive decay rate to fall to half of the original value! But from geiger counter readings one can infer the actual number of uranium atoms decomposing per minute in a sample, and from a chemical analysis one can measure the total amount of uranium in the sample. These two results together allow the half-life to be calculated. Finally, there is a different method again for isotopes that are intermediates in a long decay series. Ra-226 (radium) is a good example. Ra-226 is formed in radioactive decay of Th-230, which originally comes from U-238. But Ra-226 itself decays to Rn-222 (radon) and eventually to Pb-208 (lead). In a series of decays like this, all of the intermediates eventually reach a steady state, where the rate of radium production exactly equals the rate of its removal; in fact, you can infer equal rates for every reaction down the decay series. So the rate of Ra-226 decay must equal the rate of U-238 decay. This leads to the interesting result that (concentration of Ra-226)/(concentration of U-238) = (half-life of Ra-226)/ (half-life of U-238) That is, if you know the half-life of U-238, you can determine the half- life of Ra-226 simply by doing a chemical assay of the uranium and radium in your sample; there is no need to make any further measurements on the radioactivity! Of course that is not nearly as easy as it sounds, because there is only about 0.3 mg of radium per kg of uranium in uranium ore. But it means that when Marie Curie first isolated radium, she automatically had a pretty good estimate of its half-life along with her radium assay.
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