Radioisotopic analysis

As a result of these inconsistencies, the very same amino acid extracts that had been used to produce the contentious AAR dates were independently dated by the AMS method at the Oxford Radiocarbon Accelerator Unit of the Research Laboratory for Archaeology and the History of Art, University of Oxford (OxA numbers Bada et al., 1984) and the NSF Accelerator Facility for Radioisotope Analysis, University of Arizona, Tucson (AA numbers). 

Table III. Radioisotope Analysis of Second- and Third-Cycle Waste (ICPP)...

Various techniques can be used for quantitative analysis of chemical composition, including (i) optical atomic spectroscopy (atomic absorption, atomic emission, and atomic fluorescence), (ii) X-ray fluorescence spectroscopy, (iii) mass spectrometry, (iv) electrochemistry, and (v) nuclear and radioisotope analysis [41]. Among these, optical atomic spectroscopy, involving atomic absorption (AA) or atomic emission (AE), has been the most widely used for chemical analysis of ceramic powders. It can be used to determine the contents of both major and minor elements, as well as trace elements, because of its high precision and low detection limits. 

Long-lived radioisotope analysis is based on the measurement of a very small isotopic ratio. Usually, small amounts of chemically prepared pure samples (in the form of elements or compounds) rather than the original samples are used in the ion source. The element-preconcentration is performed during the preparation of the AMS sample. Since the natural abundances of long-lived radioisotopes are usually very low in terrestrial materials, the contamination by the radioisotope itself from the environment is not a severe problem. The background may come from interferences of atomic and molecular species, stable isobars and isotopes, which can be discriminated effectively by AMS. Consequently, high sensitivities can be achieved in the AMS measurements of the radioisotopes ( °Be, Al, Si, Cl, Ca, etc.) for tracer studies. The... 

It is not necessary that there be two isotopes in both the sample and the spike. One isotope in the sample needs to be measured, but the spike can have one isotope of the same element that has been produced artificially. The latter is often a long-lived radioisotope. For example, and are radioactive and all occur naturally. The radioactive isotope does not occur naturally but is made artificially by irradiation of Th with neutrons. Since it is commercially available, this last isotope is often used as a spike for isotope-dilution analysis of natural uranium materials by comparison with the most abundant isotope ( U). 

The neutrons in a research reactor can be used for many types of scientific studies, including basic physics, radiological effects, fundamental biology, analysis of trace elements, material damage, and treatment of disease. Neutrons can also be dedicated to the production of nuclear weapons materials such as plutonium-239 from uranium-238 and tritium, H, from lithium-6. Alternatively, neutrons can be used to produce radioisotopes for medical diagnosis and treatment, for gamma irradiation sources, or for heat energy sources in space. 

A large number of radiometric techniques have been developed for Pu analysis on tracer, biochemical, and environmental samples (119,120). In general the a-particles of most Pu isotopes are detected by gas-proportional, surface-barrier, or scintillation detectors. When the level of Pu is lower than 10 g/g sample, radiometric techniques must be enhanced by preliminary extraction of the Pu to concentrate the Pu and separate it from other radioisotopes (121,122). Alternatively, fission—fragment track detection can detect Pu at a level of 10 g/g sample or better (123). Chemical concentration of Pu from urine, neutron irradiation in a research reactor, followed by fission track detection, can achieve a sensitivity for Pu of better than 1 mBq/L (4 X 10 g/g sample) (124). 

Radiochemical tracers, compounds labeled with radioisotopes (qv), have become one of the most powerful tools for detection and analysis in research, and to a limited extent in clinical diagnosis (see Medical IMAGING TECHNOLOGY). A molecule or chemical is labeled using a radioisotope either by substituting a radioactive atom for a corresponding stable atom in the compound, such as substituting for H, for or for P, and for for... 

Elements with multiple stable isotopes may produce several radioisotopes that can be measured to assure the accuracy of the analysis. For example, Zn has five stable isotopes. The isotope Zn will produce the radioisotope Zn, and Zn will produce the radioisotope Zn. Both of these radioisotopes can provide an independent measurement of the Zn concentration and therefore can be used to check the consistency and quality of the analysis. On the other hand, Zn will produce Zn, which is nonradioactive and therefore cannot be used in NAA. 

Another application involves the measurement of copper via the radioisotope Cu (12.6-hour half-life). Since Cu decays by electron capture to Ni ( Cu Ni), a necessary consequence is the emission of X rays from Ni at 7.5 keV. By using X-ray spectrometry following irradiation, sensitive Cu analysis can be accomplished. Because of the short range of the low-energy X rays, near-surface analytical data are obtained without chemical etching. A combination of neutron activation with X-ray spectrometry also can be applied to other elements, such as Zn and Ge. 

IEC continues to have numerous applications to the detection and quantification of various inorganic ions.1 1 This is particularly true in water analysis.5-14 Inorganic ions in a variety of other sample types, such as food and beverages,1518 rocks,19-23 biological fluids, (blood, urine, etc.),24-31 pharmaceutical substances,32 33 concentrated acids,34 alcohols,35 and cleanroom air36 have also been analyzed by IEC. IEC has also been employed in isotopic separation of ions,37 including the production of radioisotopes for therapeutic purposes.3839 Typical IEC sample matrices are complex, and may contain substances that interfere with measurement of the ion(s) of interest. The low detection limits required for many IEC separations demand simple extraction procedures and small volumes to avoid over-dilution. Careful choice and manipulation of the eluent(s) may be needed to achieve the desired specificity, especially when multiple ions are to be determined in a single sample. 

H13. Hirono, A., Miwa, S., Fujii, H Ishida, F., Yamada, K., and Kubota, K., Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by non-radioisotopic singlestrand conformation polymorphism (SSCP) analysis. Blood 83,3363-3368 (1994). 

One of the first decisions to be made when designing an experiment is the method of detection to be used with a particular solute. If radiolabeled material is available, a simple method of analysis is to count the radiolabel appearing in the receiver compartment as a function of time. While convenient, this can be a dangerous practice. Depending upon the type of radioisotope, its position in the molecule, and its specific activity, radiolabeled compounds can be subject to a variety of chemical and solution-catalyzed degradation pathways. If the stock solution contains a significant amount of radioactive impurities or generates them as a result of solution instability, then the possibility for preferential transport of... 

A mixture is being assayed by radioisotope dilution analysis. 10 mg of the labelled analyte (0.51 pCi mg-1) was added. 1.5 mg of the pure analyte was separated and its specific activity measured and found to be 0.042 pCi mg1. What was the amount of analyte in the original sample ... 

Dynamic SIMS is used for depth profile analysis of mainly inorganic samples. The objective is to measure the distribution of a certain compound as a function of depth. At best the resolution in this direction is < 1 nm, that is, considerably better than the lateral resolution. Depth profiling of semiconductors is used, for example, to monitor trace level elements or to measure the sharpness of the interface between two layers of different composition. For glass it is of interest to investigate slow processes such as corrosion, and small particle analyses include environmental samples contaminated by radioisotopes and isotope characterization in extraterrestrial dust. 

We have recently modified U7) one of the several radiochemical methods (U5) which have been used for surface electrochemistry investigations in order to characterize adsorption on well-defined, single crystal electrodes. Below, we will describe the technique and identify some challenging issues which we will be able to address. The proposed method is sensitive to a few percent of a monolayer at smooth surfaces, is nondestructive and simple to use. The radiochemical measurements can be made with all compounds which can be labelled with reasonably long-lived, preferably g- emitting radioisotopes. We believe this technique will fulfill the quantitative function in in situ surface analysis as Auger spectroscopy currently does in vacuum, ex situ characterization of electrodes. 

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