- #1
Chemistlsc
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- TL;DR Summary
- what are the advantages of using the external source for a Quench Indicating Parameter vs without it? And can the internal standard method be applied with the external source? Why must the same cocktail be used for both the quench set and samples?
Good day,
My background is in chemistry but my work now revolves around the liquid scintillation counter and so I have a couple of couple of questions on the usage of an external source like how typical.
I've read that most Quench Indicating Parameters involve the preparation of a quench set which comprises of a known amount of active standard, and varying amounts of quenching agent such as nitromethane. Then by exposing these quenched standards to the external source a measurement of a Quench Indicating Parameter like QPE, tSIE, etc is achieved and plotted against the efficiency (a quench curve). Following this, when we analyze a sample we measure the sample's Quench Indicating Parameter to determine its efficiency. And then calculate its activity by dividing the measured CPM/efficiency.
I have the following queries:
1. Is this form of Quench Indicating Parameter any better than those without an external source? Mostly because this is an additional standard that incurs additional cost, and so I'm not sure if its worth it. For example, for the HIDEX systems I see that I can plot a quench curve suing TDCR, and this does not require any external source.
2. Instead of using these Quench Indicating Parameters with the external source, is it possible to do it with via the "internal standard" method? Whereby a sample is counted, then a known amount of standard (DPM) is spiked into the sample. Then taking the additional counts/DPM we get the efficiency of the sample. Instead of spiking the standard, can we use the external source to "spike" a known amount of electrons into the system?
3. Must the cocktail I use be the same for the quench set and my samples? My logic is that the "quench" measured with the Quench Indicating Parameter is an all encompassing effect so by plotting a quench curve, I don't have to use the same cocktail anymore. However, I've seen tables from PerkinElmer whereby using a different cocktail from the quench set can result in a large deviations in the determined efficiency. I don't really understand why this is the case since I would think that the Quench Indicating Parameter would take all these compositional differences into account, and so long as the Quench Indicating Parameter of the sample is within the quench set's "calibration range" it should be fine.
My background is in chemistry but my work now revolves around the liquid scintillation counter and so I have a couple of couple of questions on the usage of an external source like how typical.
I've read that most Quench Indicating Parameters involve the preparation of a quench set which comprises of a known amount of active standard, and varying amounts of quenching agent such as nitromethane. Then by exposing these quenched standards to the external source a measurement of a Quench Indicating Parameter like QPE, tSIE, etc is achieved and plotted against the efficiency (a quench curve). Following this, when we analyze a sample we measure the sample's Quench Indicating Parameter to determine its efficiency. And then calculate its activity by dividing the measured CPM/efficiency.
I have the following queries:
1. Is this form of Quench Indicating Parameter any better than those without an external source? Mostly because this is an additional standard that incurs additional cost, and so I'm not sure if its worth it. For example, for the HIDEX systems I see that I can plot a quench curve suing TDCR, and this does not require any external source.
2. Instead of using these Quench Indicating Parameters with the external source, is it possible to do it with via the "internal standard" method? Whereby a sample is counted, then a known amount of standard (DPM) is spiked into the sample. Then taking the additional counts/DPM we get the efficiency of the sample. Instead of spiking the standard, can we use the external source to "spike" a known amount of electrons into the system?
3. Must the cocktail I use be the same for the quench set and my samples? My logic is that the "quench" measured with the Quench Indicating Parameter is an all encompassing effect so by plotting a quench curve, I don't have to use the same cocktail anymore. However, I've seen tables from PerkinElmer whereby using a different cocktail from the quench set can result in a large deviations in the determined efficiency. I don't really understand why this is the case since I would think that the Quench Indicating Parameter would take all these compositional differences into account, and so long as the Quench Indicating Parameter of the sample is within the quench set's "calibration range" it should be fine.