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Activation analysis nuclear reactions used

Bromine-82 has a half-life of about 36 hours this is not sufficient for the isotope to be used conveniently in tracer work especially if labelled reagents have first to be prepared and purified. Low concentrations of bromine in small specimens of organic materials, such as polymers, can be determined by the method of neutron activation analysis (2). The various substances are prepared using ordinary bromine and then samples are bombarded with thermal neutrons so that the nuclear reaction 81Br(n, y)82Br occurs. Activity is therefore induced in the samples comparison with standards treated similarly permits determination of the bromine contents of the unknowns. For this technique to be applicable, it is necessary to have access to a powerful source of thermal neutrons. Neutron activation analysis can be used for the determination of very low concentrations of many elements and its general features have been fully discussed (3). [Pg.3]

Neutron activation analysis (NAA) making use of the nuclear reaction " N(n,2n) N can be applied for bulk determination of nitrogen. [Pg.3008]

It is probably easiest to classify activation analysis according to the type of nuclear reaction used to generate the analytical signal. As shown in O Fig. 30.1, the commonly used activation... [Pg.1563]

All the techniques discussed here involve the atomic nucleus. Three use neutrons, generated either in nuclear reactors or very high energy proton ajccelerators (spallation sources), as the probe beam. They are Neutron Diffraction, Neutron Reflectivity, NR, and Neutron Activation Analysis, NAA. The fourth. Nuclear Reaction Analysis, NRA, uses charged particles from an ion accelerator to produce nuclear reactions. The nature and energy of the resulting products identify the atoms present. Since NRA is performed in RBS apparatus, it could have been included in Chapter 9. We include it here instead because nuclear reactions are involved. [Pg.645]

In the discussion that follows we refer to nuclear activation detection reactions in lieu of analysis reactions since the signals that are measured are not necessarily always from a radioactive product. Again, we will use standard nuclear physics notation in specifying nuclear reactions, namely ... [Pg.379]

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]

Until it was known that the half-life of Tc is much shorter than 10 years Herr looked for technetiimi-98 in a munber of minerals from Norway and South Africa by neutron activation analysis. This most sensitive method was also used by Alperovitch et al. and Anders et al. to detect this isotope in nature. According to the nuclear reaction... [Pg.112]

The concentration of silver nanoparticles and ions in solntions was determined by neutron activation analysis [15]. Samples were irradiated in the nuclear reactor at the Institute of Nuclear Physics, Tashkent, Uzbekistan. The product of nuclear reaction ° Ag(n,y)" Ag has the half-life Tj j=253 days. The silver concentration was determined by measnring the intensity of gamma radiation with the energy of 0.657 MeV and 0.884 MeV emitted by "" Ag. A Ge(Li) detector with a resolution of about 1.9 keV at 1.33 MeV and a 6,144-channel analyzer were used for recording gamma-ray quanta. [Pg.171]

During the late 1960s and early 1970s, neutron activation analysis provided a new way to measure bulk chemical composition. Neutron activation analysis utilizes (n,y) reactions to identify elements. A sample is placed in a nuclear reactor where thermal neutrons are captured by atoms in the sample and become radioactive. When they decay, the radioactive isotopes emit characteristic y-rays that are measured to determine abundances. Approximately 35 elements are routinely measured by neutron activation analysis. A number of others produce radioactive isotopes that emit y-rays, but their half-lives are too short to be useful. Unfortunately, silicon is one of these elements. Other elements do not produce y-ray-emitting isotopes when irradiated with neutrons. There are two methods of using neutron activation to determine bulk compositions, instrumental neutron activation analysis (INAA) and radiochemical neutron activation analysis (RNAA). [Pg.519]

Radioactivation analysis has been used to measure bromine in polymers (37—39) and recently a novel technique for trace oxygen has been reported (40). Any polymer or other material (e.g. metal alkyl) which is miscible with butyl lithium solutions may be analysed since the procedure involves the intermediate production of triton particles by the nuclear reaction 6Li (n, a) t. The tritons then act as nuclear projectiles for the activation of oxygen 0 (t, n) 18F and the radioactivity due to fluorine-18 is measured. A sensitivity of 1 x 10 g in a 0.5 g sample is claimed. [Pg.136]

Activation analysis is based on the production of radioactive nuclides by means of induced nuclear reactions on naturally occurring isotopes of the element to be determined in the sample. Although irradiations with charged particles and photons have been used in special cases, irradiation with reactor thermal neutrons or 14 MeV neutrons produced by Cockcroft-Walton type accelerators are most commonly used because of their availability and their high probability of nuclear reaction (cross section). The fundamental equation of activation analysis is given below ... [Pg.50]

It is obvious, therefore, that 14 MeV neutron activation analysis can not compete with thermal neutron activation analysis as a technique for trace element analysis. In simple matrices, however, the rapid and non-destructive nature of the technique recommends its use for routine analysis of large numbers of samples for elemental abundances at the one milligram level, or above. It is unfortunate that the element carbon can not be determined by this technique. The nuclear reaction 12C(n, 2n)1 C which would be of great analytical importance is endoergic to the extent of nearly 19 MeV. This reaction is obviously not energetically possible using the 14.7 MeV neutrons produced by the 2H(3H,w)4He reaction commonly employed in most neutron generators. [Pg.54]

In order to determine the half-life, the decay scheme, and other nuclear characteristics of a radioactive nuclide, it is important to use a sample of very high radiochemical purity. In addition in the measurement of nuclear reaction cross sections, fission yields and in activation analysis, the amounts of the radioactive nuclide produced must be determined. Thus It Is also necessary to determine the yield of... [Pg.9]

Activation by high-energy neutrons is of interest if the cross sections of (n,y) reactions are too low or if the macrocomponents are too highly activated by thermal neutrons. For the purpose of activation analysis, special neutron generators have been developed. In these generators protons or deuterons with energies of the order of 0.1 to 1 MeV are used for the production of neutrons by nuclear reactions. The preferred reactions are... [Pg.342]

In the nuclear reactor the normal reaction used in activation analysis is the (n,y) induced by thermal neutrons but there are several routes by which a nuclide A of atomic number Z and mass M may be produced ... [Pg.331]

Nuclear reactions can be used to help museum directors detect whether an artwork, such as the one shown in Figure 18, is a fake. The process is called neutron activation analysis. A tiny sample from the suspected forgery is placed in a machine. A nuclear reactor in the machine bombards the sample with neutrons. Some of the atoms in the sample absorb neutrons and become radioactive isotopes. These isotopes emit gamma rays as they decay. [Pg.681]

The use of activation methods for the analysis of biological material has been reviewed by Bowen ( 7). In Instrumental Neutron Activation Analysis, the dried sample is placed in the core of a nuclear reactor where it is bombarded with neutrons. Many of the elements present in the sample undergo nuclear reactions of which the most common are the (n, y) type. The products of these reactions are radioactive and decay with the emission of gamma photons of characteristic energy. [Pg.298]

Several investigators have used neutron activation analysis (NAA) to determine the aluminium content of biological specimens both with and without some chemical processing. Instrumental neutron activation analysis involves the bombardment of a sample with neutrons and the measurement of the radioactivity induced by nuclear reactions. No chemical processing is required. Upon activation Al (100% isotopic abundance) forms the radioactive AI nuclide by a (n,y) reaction. There are a number of attractive features in this technique which include excellent sensitivity with relative independence from matrix effects and interferences. Also, there is relative freedom from contamination since the sample is analyzed directly with minimal handling. One major problem is the need to... [Pg.276]

Prompt activation analysis (Erdtmann and Petri, 1986 Alfassi, 1990) uses the prompt radiation accompanying a nuclear reaction for determining elemental or isotopic concentrations. The variety of prompt methods is large because a sample can be irradiated with various particles - neutrons, charged particles or gamma-rays. Prompt activation analysis permits the determination of several elements - about 17 elements in environmental matrices (Germani et al., 1980) - but most analysis are used for the determination of light elements (H, He, Li, B, C, N, Si, S, Cl) as well of Cd and Gd. [Pg.161]


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See also in sourсe #XX -- [ Pg.4 , Pg.385 , Pg.395 , Pg.401 ]




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