Difference between revisions of "The NAA Method"

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====== Written and developed by [http://www.mn.uio.no/kjemi/personer/vit/torbjor/index.html Prof. Tor Bjørnstad] (IFE/UiO)   ======
 
====== Written and developed by [http://www.mn.uio.no/kjemi/personer/vit/torbjor/index.html Prof. Tor Bjørnstad] (IFE/UiO)   ======
  
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====== Return to [[Neutron Activation Analysis]] ======
======Return to [[Neutron Activation Analysis]] ======
 
  
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The sequence of events occurring during the most common type of nuclear reaction used for NAA, namely the neutron capture or (n,<span class="texhtml">γ</span>) reaction, is illustrated in the figure below.  
The sequence of events occurring during the most common type of nuclear reaction used for NAA, namely the neutron capture or (n,<math>\gamma</math>) reaction, is illustrated in the figure below.  
 
  
 
[[Image:N activiation NAA method.png]]<br>  
 
[[Image:N activiation NAA method.png]]<br>  
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<br>When a neutron interacts with the target nucleus via a non-elastic collision, a compound nucleus forms in an excited state. The excitation energy of the compound nucleus is due<br>to the binding energy of the neutron within the nucleus. The compound nucleus will almost instantaneously de-excite into a more stable configuration through emission of one or<br>more characteristic prompt gamma rays. In many cases, this new configuration yields a <br>radioactive nucleus which also de-excites (or decays) by emission of one or more characteristic delayed gamma rays, but at a much slower rate according to the unique half-life of the radio-active nucleus. Depending upon the particular radioactive species, half-lives can range from fractions of a second to several years.  
 
<br>When a neutron interacts with the target nucleus via a non-elastic collision, a compound nucleus forms in an excited state. The excitation energy of the compound nucleus is due<br>to the binding energy of the neutron within the nucleus. The compound nucleus will almost instantaneously de-excite into a more stable configuration through emission of one or<br>more characteristic prompt gamma rays. In many cases, this new configuration yields a <br>radioactive nucleus which also de-excites (or decays) by emission of one or more characteristic delayed gamma rays, but at a much slower rate according to the unique half-life of the radio-active nucleus. Depending upon the particular radioactive species, half-lives can range from fractions of a second to several years.  
  
In principle, therefore, with respect to the time of measurement, NAA falls into two categories: (1) prompt gamma-ray neutron activation analysis (PGNAA), where measurements take place during irradiation, or (2) delayed gamma-ray neutron activation analysis (DGNAA), where the measurements follow radioactive decay. The latter operational mode is more common; thus, when one mentions NAA it is generally assumed that measurement of the delayed gamma rays is intended. About 70% of the elements have properties suitable for measurement by NAA. <br><br>
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In principle, therefore, with respect to the time of measurement, NAA falls into two categories: (1) prompt gamma-ray neutron activation analysis (PGNAA), where measurements take place during irradiation, or (2) delayed gamma-ray neutron activation analysis (DGNAA), where the measurements follow radioactive decay. The latter operational mode is more common; thus, when one mentions NAA it is generally assumed that measurement of the delayed gamma rays is intended. About 70% of the elements have properties suitable for measurement by NAA. <br><br>  
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[[Category:Nuclear_Properties]][[Category:Laboratory_exercise]][[Category:Neutron_Activation_Analysis]]

Revision as of 10:24, 28 June 2012

Written and developed by Prof. Tor Bjørnstad (IFE/UiO) 
Return to Neutron Activation Analysis

The sequence of events occurring during the most common type of nuclear reaction used for NAA, namely the neutron capture or (n,γ) reaction, is illustrated in the figure below.

N activiation NAA method.png

Diagram illustrating the process of neutron capture by a target nucleus followed by the emission of gamma rays.


When a neutron interacts with the target nucleus via a non-elastic collision, a compound nucleus forms in an excited state. The excitation energy of the compound nucleus is due
to the binding energy of the neutron within the nucleus. The compound nucleus will almost instantaneously de-excite into a more stable configuration through emission of one or
more characteristic prompt gamma rays. In many cases, this new configuration yields a
radioactive nucleus which also de-excites (or decays) by emission of one or more characteristic delayed gamma rays, but at a much slower rate according to the unique half-life of the radio-active nucleus. Depending upon the particular radioactive species, half-lives can range from fractions of a second to several years.

In principle, therefore, with respect to the time of measurement, NAA falls into two categories: (1) prompt gamma-ray neutron activation analysis (PGNAA), where measurements take place during irradiation, or (2) delayed gamma-ray neutron activation analysis (DGNAA), where the measurements follow radioactive decay. The latter operational mode is more common; thus, when one mentions NAA it is generally assumed that measurement of the delayed gamma rays is intended. About 70% of the elements have properties suitable for measurement by NAA.