Gamma Spectroscopy for Estimating Radiological Risk in Rocks

AI Thread Summary
The discussion focuses on using gamma spectroscopy to estimate the radiological risk from U-238, Th-232, and K-40 in rock samples. The NaI(TI) crystal and associated equipment are used to detect gamma rays, with the user seeking methods to calculate the activity of identified radionuclides. Calibration is crucial for accurate activity measurement, ideally using a source with known activity, though estimates can be made without one, albeit with increased uncertainty. Key concepts such as peak area, efficiency of the detector, and branching ratios are discussed as they relate to activity concentration. A suggestion is made to use potassium chloride (KCl) as a makeshift standard for K-40 to aid in calibration.
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Am currently doing an undergraduate project work on 'estimation of radiological risk pose by U-238, th-232 and K-40 in rock samples' . The instrument I'll use are NaI(TI) crystal for scintilation were the gamma rays from the source(my rock samples) interact with the crystal through photoelectric effect, compton effect & pair production thus releasing photoelectrons, A photomultiplier tube (PMT) optically couple to the detector- to energize the photoelectrons from the detector, multichannel analyzer (MCA) plus an amplify with A-D converter, and a computer with the software winDAS installed to display the spectrum in histogram with count/second on the vertical axis and channel(energy in MeV) on horizontal axis.
The radionuclides present in the sample is identified if you trace it's energy on the spectrum, eg K-40 who's E is 1.460MeV will be traced.
Now, once the spectra corresponding to K-40 energy is identified how do i CALCULATE the ACTIVITY(Bq) of this nuclide and that of others to be identified?.
Thanks in advance!
 
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You (well, your software) can count the number of detected gamma rays.
Together with the geometry of the setup (which fraction of photons reaches your detector?), radiation length calculations (which fraction interacts in your detector?), background rates, effective deadtimes and some additional things I forgot, you can find the activity of the sample.
 
Ok, can you give me the explicit expression that bind this informations as a whole?- that will allow me compute the activity
 
It depends on your setup, there is no way to do this calibration if you do not have access to the setup itself.
Do you have a source with known activity? This will make the calibration easier.
 
Thanks, I'll carry out the experiment tommorow, I do not have a source with known activity, is there no other way to caliberate without a source? And how does finding the activity depends on my set-up?
 
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And how does finding the activity depends on my set-up?
By the effects I mentioned. The geometry, the efficiency of the detector and so on.
is there no other way to caliberate without a source?
It is possible to get an estimate, but it will need a lot of work to do that properly.

If you work with radioactive samples, it should be possible to get a source with known activity.
 
Thanks alot, I'll get back to you when i start the analysis.
 
i've been delaying the experiment because I've got no standard source, can i go on without it?
 
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The activity measurement will get larger uncertainties (and much more work), but it is possible to find some estimate.
 
  • #10
ok, what is peak area?peak intensity?efficiency of detector?branching ratio of the source? Peak centroid?and FWHM? How do they relate with the activity concentration of a nuclide at that peak?..i know my questions are plenty ,i just need your help!
 
  • #11
What do you mean with peak area and peak intensity? Peak with respect to what?

efficiency of detector?
(detected particles) / (particles going though the detector)

branching ratio of the source?
I know branching ratios of particles... the fraction of particles decaying to some specific set of products.

Peak centroid?
Context?

and FWHM?
Wikipedia helps - not only there, but also at the other questions.
 
  • #12
i'll try it, thanks alot
 
  • #13
A good way to create a makeshift standard for K-40 is to get some of the salt substitute (which is KCl). Measure out a known mass, and with the isotopic abundance value you should be able to get the mass of K-40, which will give you the activity. It isn't exact because of impurities, but it's certainly a better estimate than anything else I can think of.
 

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