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Neutron activation analysis prompt

Two elemental analyzer systems have been developed, the "Continuous On-line Nuclear Assay of Coal", CONAC, (Science Application, Inc., Palo Alto, CA) and "The Elemental Analyzer" (MDH Industries, Inc., Monrovia, CA). Both of these units are based upon the measurement of prompt gamma rays that are emitted from a nucleus following the capture of a neutron. This technique is commonly known as prompt neutron activation analysis, PNAA. [Pg.268]

This can result in a radioactive product from the A(n, t)A reaction where A is the stable element, n is a thermal neutron, A is the radioactive product of one atomic mass unit greater than A, and y is the prompt gamma ray resulting from the reaction. A is usually a beta and/or gamma emitter of reasonably long half-life. Where access to a nuclear reactor has been convenient, thermal neutron activation analysis has proven to be an extremely valuable nondestructive analytical tool and in many cases, the only method for performing specific analyses at high sensitivities... [Pg.356]

Z.B. Alfassi and C. Chung (eds), Prompt Gamma Neutron Activation Analysis, CRC Press, Boca Raton, FL (1995). [Pg.679]

Figure 2.13 Schematic diagram of the nuclear processes involved in neutron activation analysis. Prompt gamma neutron activation analysis (PGNAA) occurs within the reactor delayed gamma NAA (DGNAA) occurs at some remote site. (After Glascock, 1994 Fig. 1. John Wiley Sons Limited. Reproduced with permission.)... Figure 2.13 Schematic diagram of the nuclear processes involved in neutron activation analysis. Prompt gamma neutron activation analysis (PGNAA) occurs within the reactor delayed gamma NAA (DGNAA) occurs at some remote site. (After Glascock, 1994 Fig. 1. John Wiley Sons Limited. Reproduced with permission.)...
The y particle is emitted virtually instantaneously on the capture of the neutron, and is known as a prompt y - it can be used analytically, in a technique known as prompt gamma neutron activation analysis (PGNAA), but only if such y s can be measured in the reactor during irradiation. Under the conditions normally used it would be lost within the nuclear reactor. In this reaction, no other prompt particle is emitted. The isotope of sodium formed (24Na) is radioactively unstable, decaying by beta emission to the element magnesium (the product nucleus in Figure 2.13), as follows ... [Pg.52]

Prompt gamma neutron activation analysis (PGNAA)... [Pg.128]

Glascock, M.D., Spalding, T. G., Biers, J. C., and Corman, M.F. (1984). Analysis of copper-based metallic artefacts by prompt gamma-ray neutron activation analysis. Archaeometry 26 96-103. [Pg.365]

Since the mid-1960s, a variety of analytical chemistry techniques have been used to characterize obsidian sources and artifacts for provenance research (4, 32-36). The most common of these methods include optical emission spectroscopy (OES), atomic absorption spectroscopy (AAS), particle-induced X-ray emission spectroscopy (PIXE), inductively coupled plasma-mass spectrometry (ICP-MS), laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS), X-ray fluorescence spectroscopy (XRF), and neutron activation analysis (NAA). When selecting a method of analysis for obsidian, one must consider accuracy, precision, cost, promptness of results, existence of comparative data, and availability. Most of the above-mentioned techniques are capable of determining a number of elements, but some of the methods are more labor-intensive, more destructive, and less precise than others. The two methods with the longest and most successful histoty of success for obsidian provenance research are XRF and NAA. [Pg.527]

In PIGE the y-emission is usually prompt. If very low amounts of trace elements have to be detected it can be advantageous to use a delayed decay. In this case, the technique is called charged particle activation (CPA) and is an analogue to neutron activation analysis (NAA). It has the advantage that the prompt background from interfering reactions is completely removed as irradiation and analysis are completely separated in time. This also allows to remove external contaminants in the short time between irradiation and measurement which further improves detection limits. A comprehensive description of the technique can be found in the ion beam analysis handbook [2], For 19F CPA is conceivable in special cases via the 19F(d,dn)18F reaction. However, we have found only one application in the literature [64],... [Pg.226]

The most utilized methods include X-ray fluorescence (XRF), atomic absorption spectroscopy (AAS), activation analysis (AA), optical emission spectroscopy (OES) and inductively coupled plasma (ICP), mass spectroscopy (MS). Less frequently used techniques include ion-selective electrode (ISE), proton induced X-ray emission (PIXE), and ion chromatography (IC). In different laboratories each of these methods may be practiced by using one of several optional approaches or techniques. For instance, activation analysis may involve conventional thermal neutron activation analyses, fast neutron activation analysis, photon activation analysis, prompt gamma activation analysis, or activation analysis with radio chemical separations. X-ray fluorescence options include both wave-length and/or energy dispersive techniques. Atomic absorption spectroscopy options include both conventional flame and flameless graphite tube techniques. [Pg.21]

Figure 1. Histogram of detection limits for neutron activation analysis (NAA) and neutron-capture prompt gamma-ray activation analysis (PGAA). Data from Reference 15. Figure 1. Histogram of detection limits for neutron activation analysis (NAA) and neutron-capture prompt gamma-ray activation analysis (PGAA). Data from Reference 15.
Prompt gamma-activation analysis and neutron activation-mass spectrometry techniques have been developed that can accurately measure boron in biomaterials (Anderson et al. 1990, 1994). One major... [Pg.1253]

Anderson DL, Cunningham WC and Mackey EA (1990) Neutron capture prompt-gamma activation analysis of foods. Biol Trace Elem Res 27 613-622. [Pg.1259]

Instrumental neutron activation analysis (thermal, INAA epithermal, EINAA, prompt gamma PGNAA) (INAA)... [Pg.1546]

Some relevant terms for activation analysis are activation analysis, neutron activation analysis (NAA), instrumental neutron activation analysis (INAA), neutron activation analysis with radiochemical separation (RNAA), photon activation, neutron capture prompt gamma activation analysis (PGAA), charged particle activation, autoradiography, liquid scintillation counting, nuclear microprobe analysis, radiocarbon (and other element) dating, radioimmunoassay, nuclear track technique, other nuclear and radiochemical methods. Briefly, the salient features of some of the more popular techniques are as follows ... [Pg.1580]

TNPGAA thermal neutron prompt gamma activation analysis... [Pg.1694]

TNPGNAA thermal neutron prompt gamma neutron activation analysis TOF-MS time of flight mass spectrometry toxicokinetics study of the quantitative action of a poison in an organism over a period of time, especially the processes of absorption, distribution, biotrans formation and excretion... [Pg.1694]

The history of neutron activation analysis goes back to the middle of the 1930s when it was first described by G. Hevesy and H. Levi at the Niels Bohr Institute in Copenhagen. The principle of the technique is that elements can be made radioactive by exposure to neutron irradiation. Two types of physiological processes are associated with this activation one prompt and one delayed. Classically, neutron activation analysis is based on the detection of the delayed event, viz. the characteristic radiation emitted during the decay -with a specific half-life (ti/a) - of the unstable nuclei formed by (n,y) reaction. [Pg.147]

In neutron activation analysis, an activation of a sample material is accomplished by placing the sample in some position within the neutron environment. At the time the sample is exposed to neutrons, a compound nucleus is formed as the result of the interaction of a neutron with the nucleus of a stable isotope of the element being determined. The compound nucleus i.e. the end-product of an excitation process caused by both the kinetic and binding energy of the neutron with the nucleus, instantaneously loses its excess energy by a transformation to a more stable isotope by emitting prompt radiations. As a result of this event, another stable nuclide or a radioactive isotope is formed. This radioisotope then becomes the activation, or isotopic, indicator of the element of interest. [Pg.351]

Neutron-Induced Prompt Gamma Activation Analysis (PGAA). 1565... [Pg.1553]

Molnar GL (ed) (2003) Handbook of prompt gamma activation analysis with neutron beams. Kluwer Acadamic, Dordrecht... [Pg.1615]


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