Radioactive isotopes separation

Uranium oxide [1344-57-6] from mills is converted into uranium hexafluoride [7783-81-5] FJF, for use in gaseous diffusion isotope separation plants (see Diffusion separation methods). The wastes from these operations are only slightly radioactive. Both uranium-235 and uranium-238 have long half-Hves, 7.08 x 10 and 4.46 x 10 yr, respectively. Uranium enriched to around 3 wt % is shipped to a reactor fuel fabrication plant (see Nuclear REACTORS, NUCLEAR FUEL reserves). There conversion to uranium dioxide is foUowed by peUet formation, sintering, and placement in tubes to form fuel rods. The rods are put in bundles to form fuel assembHes. Despite active recycling (qv), some low activity wastes are produced. 

The licensing process consists of two steps construction and operating license that must be completed before fuel loading. Licensing covers radiological safety, environmental protection, and antitru,st considerations. Activities not defined as production or utilization of special nuclear material (SNM), use simple one-step. Materials Licenses, for the possession of radioactive materials. Examples are uranium mills, solution recovery plants, UO fabrication plants, interim spent fuel storage, and isotopic separation plants. 

Until the advent of modem physical methods for surface studies and computer control of experiments, our knowledge of electrode processes was derived mostly from electrochemical measurements (Chapter 12). By clever use of these measurements, together with electrocapillary studies, it was possible to derive considerable information on processes in the inner Helmholtz plane. Other important tools were the use of radioactive isotopes to study adsorption processes and the derivation of mechanisms for hydrogen evolution from isotope separation factors. Early on, extensive use was made of optical microscopy and X-ray diffraction (XRD) in the study of electrocrystallization of metals. In the past 30 years enormous progress has been made in the development and application of new physical methods for study of electrode processes at the molecular and atomic level. 

Radioactive isotopes provide a very convenient way of monitoring the fate or metabolism of compounds that contain the isotopes. When used in this way, the isotope is described as a tracer and compounds into which the radioactive atom has been introduced are said to be labelled or tagged. The labelled molecules need only comprise a very small proportion of the total amount of the unlabelled radioactive substance because they act in the same way as the non-radioactive substance but can be detected very much more easily. The varied applications of tracers in biochemistry range from studies of metabolism in whole animals or isolated organs to sensitive quantitative analytical techniques, such as radioimmunoassay. Phosphorus-32 is used in work with nucleic acids, particularly in DNA sequencing and hybridization techniques. In these instances the isotope is used as a means of visualizing DNA separations by autoradiographic techniques. 

Secondary isotope effects are small. In fact, most of the secondary deuterium KIEs that have been reported are less than 20% and many of them are only a few per cent. In spite of the small size, the same techniques that are used for other kinetic measurements are usually satisfactory for measuring these KIEs. Both competitive methods where both isotopic compounds are present in the same reaction mixture (Westaway and Ali, 1979) and absolute rate measurements, i.e. the separate determination of the rate constant for the single isotopic species (Fang and Westaway, 1991), are employed (Parkin, 1991). Most competitive methods (Melander and Saunders, 1980e) utilize isotope ratio measurements based on mass spectrometry (Shine et al., 1984) or radioactivity measurements by liquid scintillation (Ando et al., 1984 Axelsson et al., 1991). However, some special methods, which are particularly useful for the accurate determination of secondary KIEs, have been developed. These newer methods, which are based on polarimetry, nmr spectroscopy, chromatographic isotopic separation and liquid scintillation, respectively, are described in this section. The accurate measurement of small heavy-atom KIEs is discussed in a recent review by Paneth (1992). 

The same problems of separating radioactive materials occur of course with the fission products of uranium where the task is often to separate a much larger number of different carrier-free radio-elements than occurs in normal targets. The mixture is complex and consists of elements from zinc to terbium and several hundred radioactive isotopes of varying half-life. 

Einsteinium isotopes are separated on an ion exchange column and eluted with a solution of ammonium citrate. Radioactive isotopes are identified by an activity detector. 

The XPS valence band spectra for the dioxides of the transuranium elements (from Np to Bk) have been presented in an extensive and pioneering work that also includes core level spectra and has been for a long time the only photoemission study on highly radioactive compounds. High resolution XPS spectra (AE = 0.55 eV) were recorded on oxidized thin metal films (30 A) deposited on platinum substrates with an isotope separator. (The oxide films for Pu and the heavier actinides may contain some oxides with lower stoichiometry, since starting with Pu, the sesquioxides of the heavier actinides begin to form in high vacuum conditions.)... 

Many radioisotopes exist, but not all radioisotopes are created equal. Radioisotopes break down through three separate decay processes (or decay modes) alpha decay, beta decay, and gamma decay. The following sections show you equations detailing each type of decay. Note The symbols showing the isotope notation for each radioactive isotope cire as follows or 2 Y, where... 

Closely related to tracer analysis is the method of isotopic dilution analysis. Here, instead of checking the effectiveness of a method from known amounts of an element in the sample, and of its radioactive isotope, one knows only the amount of radioactive isotope added, and by precipitating or otherwise separating the total amount of that element present, and then measuring its radioactivity, one determines its amount, and hence the amount present in the original sample. 

Crown ethers and cryptands, either alone or fixed on a polymer support [2.89], have been used in many processes, including selective extraction of metal ions, solubilization, isotope separation [2.90], decorporation of radioactive or toxic metals [2.17, 2.49], and cation-selective analytical methods [2.89, 2.91, 2.92] (see also Sect. 8.2.2 and 8.4.5). A number of patents have been granted for such applications. 

Strontium. Sr at no 38 at wt 87.62 valence 2 two important radioactive isotopes (out of 12), Sr-89 and Sr-90 four stable isotopes, 88 (82.56% abundance), 86 (9.86% abundance), 87 (7.02% abundance), 84 (0.56% abundance) silvery-white metal, face-centered cubic structure brief exposure to air results in the yel oxide mp 752°, 757°, 769° (separate values) bp 1366°, 1384°, 1390° (separate values) d 2.6g/cc. Sol in acids, ethanol and liq ammonia. CA Registry No [7440-24-6]. Occurs in nature as the sulfate celestine or the carbonate strontianite also found in small quantities associated with Ba, Ca, Pb or K minerals. Prepn is by a) electrolysis of molten Sr chloride in a graphite crucible with cooling of the upper cathodic space to isolate the Sr vapors, or b) thermal redd of the oxide... 

Developing an Accelerated Radioactive Beams Facility Using an On-Line Isotope Separator as an Injector... 

High yields of separated, radioactive ions (up to 1010 atoms/sec yA of incident protons at on-line isotope separators (ISOL), e.g. 

---