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Isotopes, radium

The liquid mine wastes are mainly represented by underground drainage waters (up to 2000 m3/day and even more), as well as low radioactive waste water from uranium treatment plants (from 100 up to 300 m3/day). The uranium isotopes, radium-226, thorium-230, polonium-210, lead-210 are the most dangerous. Their total activity in waste waters reaches often 10-50 Bq/L at the MPC values for natural waters of 0.111 Bq/L. [Pg.226]

Radiums most important use is as a source of radiation in industry, medicine, and laboratories. The isotope radium-226, which is the most abundant of all the 25 isotopes and has a half-life of 1630 years, is the only useful form of the element. It is used in the medical treatment of malignant cancer growth. It kills cancer cells that have spread throughout the body. [Pg.83]

The one-dimensional diffusion-decay equation of the excess radon activity, C c (i.e., the radon activity exceeding the activity of its parent isotope radium-226) is given by ... [Pg.1029]

Some of the radiation from radium is constantly being released into the environment. It is this release of radiation that causes concern about the safety of radium and all other radioactive substances. Each isotope of radium releases radiation at its own rate. One isotope, radium-224 for example, releases half of its radiation in about three and a half days whereas another isotope, radium-226, releases half of its radiation in about 1,600 years. [Pg.10]

Radium may be transported in the atmosphere in association with particulate matter. It exists primarily as a divalent ion in water, and its concentration is usually controlled by adsorption-desorption mechanisms at solid-liquid interfaces and by the solubility of radium-containing minerals. Radium does not degrade in water other than by radioactive decay at rates that are specific to each isotope. Radium may be readily adsorbed by earth materials consequently, it is usually not a mobile constituent in the environment. It may be bioconcentrated and bioaccumulated by plants and animals, and it is transferred in food chains from lower trophic levels to humans. [Pg.55]

Significant concentrations of contaminant radium may be submicromolar. Therefore, radiochemical separations are commonly employed that make use of a carrier, a nonradioactive element with chemical properties similar to those of radium. For radium, barium is the element of choice, and radium is coprecipitated from solution with barium sulfate, BaSCH Correction for losses in the precipitation procedure may be made by adding a tracer consisting of an isotope of radium not expected in the sample and noting its recovery at the end of the analytical procedure. The isotope radium- 223 can be used for this purpose. [Pg.65]

The first example [33] was thorium emanation, Rn (diffusing from thorium compounds now known to contain Ra in approximate equilibrium with the ancestor radiothorium , Th), having exponential decay of its radioactivity with a half-life tjyj close to one minute. The weak point about the three emanations and their radioactive deposit (such as the polonium isotopes radium A , Po, and thorium A , Po) was the fact that their character as elements, rather than some kind of mobile ephemeral contamination, was only firmly established a few years later. [Pg.235]

Radium is the last of the alkafine earth metals comprising the second column of the Periodic Table. While there are twenty-five known isotopes of radium (only four of which are found naturally), all of them are radioactive. Of these isotopes, radium-226 is the most common, with a half-fife of about 1,600 years. [Pg.1084]

Twenty isotopes are known. Radon-22, from radium, has a half-life of 3.823 days and is an alpha emitter Radon-220, emanating naturally from thorium and called thoron, has a half-life of 55.6 s and is also an alpha emitter. Radon-219 emanates from actinium and is called actinon. It has a half-life of 3.96 s and is also an alpha emitter. It is estimated that every square mile of soil to a depth of 6 inches contains about 1 g of radium, which releases radon in tiny amounts into the atmosphere. Radon is present in some spring waters, such as those at Hot Springs, Arkansas. [Pg.152]

Gr. aktis, aktinos, beam or ray). Discovered by Andre Debierne in 1899 and independently by F. Giesel in 1902. Occurs naturally in association with uranium minerals. Actinium-227, a decay product of uranium-235, is a beta emitter with a 21.6-year half-life. Its principal decay products are thorium-227 (18.5-day half-life), radium-223 (11.4-day half-life), and a number of short-lived products including radon, bismuth, polonium, and lead isotopes. In equilibrium with its decay products, it is a powerful source of alpha rays. Actinium metal has been prepared by the reduction of actinium fluoride with lithium vapor at about 1100 to 1300-degrees G. The chemical behavior of actinium is similar to that of the rare earths, particularly lanthanum. Purified actinium comes into equilibrium with its decay products at the end of 185 days, and then decays according to its 21.6-year half-life. It is about 150 times as active as radium, making it of value in the production of neutrons. [Pg.157]

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 historic discovery of radium in 1898 by Marie Curie initiated a remarkable use of this isotope as an early oceanic tracer. Less than 10 years after its discovery,... [Pg.47]

Joly observed elevated "Ra activities in deep-sea sediments that he attributed to water column scavenging and removal processes. This hypothesis was later challenged with the hrst seawater °Th measurements (parent of "Ra), and these new results conhrmed that radium was instead actively migrating across the marine sediment-water interface. This seabed source stimulated much activity to use radium as a tracer for ocean circulation. Unfortunately, the utility of Ra as a deep ocean circulation tracer never came to full fruition as biological cycling has been repeatedly shown to have a strong and unpredictable effect on the vertical distribution of this isotope. [Pg.48]

In the U-Th decay series there are four radium isotopes, Ra (tj j =... [Pg.48]

Radium occurs only in association with uranium (Chapter 31) the observed ratio Ra/U is 1 mg per 3 kg, leading to a terrestrial abundance for Ra of 10 ppm. As uranium ores normally contain only a few hundred ppm of U, it follows that about 10 tonnes of ore must be processed for 1 mg Ra. The total amount of Ra available worldwide is of the order of a few kilograms, but its use in cancer therapy has been superseded by the use of other isotopes, and the... [Pg.109]

Polonium has no stable isotopes, all 27 isotopes being radioactive of these only °Po occurs naturally, as the penultimate member of the radium decay series ... [Pg.748]

Element 86, the final member of the group, is a short-lived, radioactive element, formerly known as radium-emanation or niton or, depending on which radioactive series it originates in (i.e. which isotope) as radon, thoron, or actinon. It was first isolated and studied in 1902 by E. Rutherford and F. Soddy and is now universally known as radon (from radium and the termination-on adopted for the noble gases Latin radius, ray). [Pg.889]

The final member of the group, actinium, was identified in uranium minerals by A. Debieme in 1899, the year after P. and M. Curie had discovered polonium and radium in the same minerals. However, the naturally occurring isotope, Ac, is a emitter with a half-life of 21.77 y and the intense y activity of its decay products makes it difficult to study. [Pg.944]

Radioactivity The ability possessed by some natural and synthetic isotopes to undergo nuclear transformation to other isotopes, 513 applications, 516-518 biological effects, 528-529 bombardment reactions, 514-516 diagnostic uses, 516t discovery of, 517 modes of decay, 513-514 nuclear stability and, 29-30 rate of decay, 518-520,531q Radium, 521-522 Radon, 528 Ramsay, William, 190 Random polymer 613-614 Randomness factor, 452-453 Raoult s law A relation between the vapor pressure (P) of a component of a solution and that of the pure component (P°) at the same temperature P — XP°, where X is the mole fraction, 268... [Pg.695]

The natural occurrence of the group-IIA elements ranges from common to rare e.g., Ca is 5th in the order of atomic abundance of the elements in the earth s crust. Mg is 7th, Ba and Sr are 21st and 22nd, respectively, and Be is 32nd . Radium is of extremely limited availability. It does occur naturally, although it has neither stable nor long-lived radioaetive isotopes it is found in association with U, since ll/2... [Pg.357]

C22-0092. The long-lived isotope of radium, Ra, decays by a emission with a half-life of 1622 years. [Pg.1619]

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. [Pg.25]

Subsequently, a wide array of developments in TIMS methods for uranium-series measurement occurred during the past decade including initiation of methods for measurement of long-lived radium (Volpe et al. 1991 Cohen and O Nions 1991) and protactinium isotopes (Pickett et al. 1994 Bourdon et al. 1999), development of improved sources or ionization methods for TIMS analysis, and introduction of commercially available multi-collector TIMS instruments designed specifically for uranium and thorium isotopic measurement. [Pg.32]

Radium and Protactinium. TIMS protocols for both radium and protactinium currently involve cycling the isotopes Ra and Ra (tracer or normal), and Pa and... [Pg.49]


See other pages where Isotopes, radium is mentioned: [Pg.125]    [Pg.784]    [Pg.201]    [Pg.2200]    [Pg.232]    [Pg.188]    [Pg.107]    [Pg.175]    [Pg.125]    [Pg.784]    [Pg.201]    [Pg.2200]    [Pg.232]    [Pg.188]    [Pg.107]    [Pg.175]    [Pg.14]    [Pg.340]    [Pg.155]    [Pg.206]    [Pg.34]    [Pg.34]    [Pg.38]    [Pg.48]    [Pg.170]    [Pg.110]    [Pg.292]    [Pg.358]    [Pg.27]    [Pg.43]   
See also in sourсe #XX -- [ Pg.48 ]

See also in sourсe #XX -- [ Pg.48 ]

See also in sourсe #XX -- [ Pg.48 ]




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