Neutron activation analysis: Difference between revisions
imported>Howard C. Berkowitz No edit summary |
imported>Howard C. Berkowitz (Placeholder for applicability tables) |
||
Line 10: | Line 10: | ||
The above description implies a measurement at a single point in time. Taking multiple measurements, of "prompt" and "delayed" gamma emission, adds another dimension. Two given elements might emit gammas of the same energy, but since the radioactive isotopes have different half-lives, one will stop emitting before the other. | The above description implies a measurement at a single point in time. Taking multiple measurements, of "prompt" and "delayed" gamma emission, adds another dimension. Two given elements might emit gammas of the same energy, but since the radioactive isotopes have different half-lives, one will stop emitting before the other. | ||
==Applicability== | |||
Not all elements absorb neutrons in a manner that makes them detectable by NAA, but approximately 65 do. | |||
Table goes here | |||
Some of these can be further differentiated by prompt and delayed NAA. | |||
Table goes here | |||
==Comparison with other methods== | ==Comparison with other methods== | ||
===Advantages=== | ===Advantages=== | ||
Line 21: | Line 26: | ||
*Time-efficient for analyzing many samples | *Time-efficient for analyzing many samples | ||
===Disadvantages=== | ===Disadvantages=== | ||
There must be a source of neutrons. For some applications, this must be a full-sized [[nuclear reactor]], with all the associated safety and cost consideration. Portable sources, however, work for some applications. | |||
==Major facilities== | ==Major facilities== | ||
One major NAA research facility is the [[High Flux Isotope Reactor]] at [[Oak Ridge National Laboratory]].<ref>{{citation | One major NAA research facility is the [[High Flux Isotope Reactor]] at [[Oak Ridge National Laboratory]].<ref>{{citation |
Revision as of 07:41, 17 May 2010
Neutron activation analysis (NAA) is an extremely sensitive technique of radiochemical analysis used to determine the existence and quantities of major, minor and trace elements in a material sample. As opposed to other methods in analytical chemistry, such as mass spectrometry or chromatography, it focuses entirely on the nuclei of atoms, not their molecular structure. It reports the concentrations of all elements in a sample, down to extremely low levels.
Principles
When samples are irradiated with neutrons, certain of their elements become radioactive, and emit gamma rays of various energies. "This emitted radiation is a 'fingerprint' of the element, and the amount of radiation given off at a certain energy is indicative of the amount of the element present in the sample. A comparison between specific activities induced in the standards and unknowns provides the basis for computation of elemental abundances. From this analysis, a report is issued giving elemental concentrations in the unknown sample."[1]
The above description implies a measurement at a single point in time. Taking multiple measurements, of "prompt" and "delayed" gamma emission, adds another dimension. Two given elements might emit gammas of the same energy, but since the radioactive isotopes have different half-lives, one will stop emitting before the other.
Applicability
Not all elements absorb neutrons in a manner that makes them detectable by NAA, but approximately 65 do.
Table goes here
Some of these can be further differentiated by prompt and delayed NAA.
Table goes here
Comparison with other methods
Advantages
- Inherently nondestructive. "The sample is not permanently damaged by NAA, and in the case case of forensic analysis and analysis of rare samples, such as meteorites or archeological finds, the sample can be saved and even subjected to further analysis at a later time...the sample may become slightly radioactive in NAA, the radiation in the sample decreases with time until it reaches a state similar to which it was before the NAA was performed on it."
- "detects the total elemental content, regardless of oxidation state, chemical form or physical location." [2]
- Simultaneously detects all elements in the sample
- Time-efficient for analyzing many samples
Disadvantages
There must be a source of neutrons. For some applications, this must be a full-sized nuclear reactor, with all the associated safety and cost consideration. Portable sources, however, work for some applications.
Major facilities
One major NAA research facility is the High Flux Isotope Reactor at Oak Ridge National Laboratory.[3]
Applications
Explosives
By examining both ratios of major elements (e.g., carbon, hydrogen, oxygen, nitrogen) as well as the presence of trace elements, NAA, even though explosives are molecules, has been able both to trace the source of explosions after detonation, as well as nondestructively tracing the manufacturer of explosives in situ. [4] NAA has been useful, in like manner, in tracing chemical warfare agents and nuclear materials.
Reference standards are being developed by the National Institute of Standards and Technology. [5], with available samples for RDX, TNT and HMX.
They form part of land mine detection systems, working on the explosive or a plastic casing not sensed by a metal detector.
References
- ↑ Neutron Activation Analysis Description, Nuclear Reactor Laboratory, University of Wisconsin
- ↑ Advantages of NAA over other chemical analyses, Nuclear Reactor Laboratory, University of Wisconsin
- ↑ What is Neutron Activation Analysis?, Neutron Sciences, Oak Ridge National Laboratory
- ↑ Nunes WV, da Silva AX, Crispim VR, Schirru R (2002 Jun), "Explosives detection using prompt-gamma neutron activation and neural networks.", Appl Radiat Isot. 56(6): 937-43.
- ↑ Development of NIST Standard Reference Materials for Trace Explosives Detection, National Institute of Standards and Technology