Palo Verde provides the following response:


1.       V. C. Summer would like to know what kind of in vivo counting 
protocols your nuclear plant has when you have workers with significant (>10 
mrem beta/gamma + alpha) measured internal doses.

For whole body counts that yield >10 mrem (only gamma-emitting radionuclides 
are identified in the air sample results), then the whole body count results 
are considered to provide the most accurate estimate of intake.  If alpha or 
beta-emitting radionuclides and/or low-yield gamma emitters are identified, 
then we use a combination of air sampling, in vitro measurements and whole body 
counting, as appropriate, to calculate the intake estimates.


2.       Do you follow a set counting frequency every time so that the counts 
can be done by HP Techs without input from a Staff Health Physicist or other 
qualified technically-qualified individual?

No, bioassay follow-up measurement periodicity and duration are performed as 
directed by staff HP, Dosimetry or Radiological Engineering Supervisor until 
the intake can be accurately assessed.


3.       If you ever experience significant alpha intakes at your nuclear plant 
that require you to perform in vitro bioassay (fecal and urine sampling), do 
you follow a set collection protocol for each sample type that is set up for 
being run by HP Techs without Staff HP or other technically-qualified 
individual input?

For alpha intakes sampling is done within four days of the intake and is 
typically directed by a Health Physicist on a case by case basis.


4.       Do you have separate protocols for fecal sampling and urine sampling?

Yes. For typical urine samples, see answer to #5, for acute tritium intakes, we 
wait three to four hours after the intake or one hour after the first voiding 
following the intake to allow the tritium to reach equilibrium in the urine. 
For an acute intake, continuous fecal sampling is performed for the first three 
to five days following the intake.



5.       If you use urine sampling for in vitro, do you specify 24-hr urine or 
spot urine?

The preferred method for investigative samples is a composite of voidings over 
a 24 hour period starting immediately after the individual's first voiding 
following the intake.  If this cannot be accomplished we will use the 24 hr 
urine sample.


**********************************************************************
Seth J. Kanter, CHP, RPT
Sr. Health Physicist
Palo Verde Nuclear Generating Station
Mail Sta. 7397
5801 S. Wintersburg Rd.
Tonopah, AZ 85354
Phone (623) 393-3130
Fax (623) 393-2487
Unless otherwise noted, all opinions are my own
Liviu Librescu
**********************************************************************



From: [email protected] [mailto:[email protected]] On Behalf Of 
GOWDY, GREGORY M
Sent: Wednesday, September 22, 2010 3:54 PM
To: [email protected]
Subject: Powernet: In Vivo and In Vitro Counting Protocols


6.       V. C. Summer would like to know what kind of in vivo counting 
protocols your nuclear plant has when you have workers with significant (>10 
mrem beta/gamma + alpha) measured internal doses.

7.       Do you follow a set counting frequency every time so that the counts 
can be done by HP Techs without input from a Staff Health Physicist or other 
qualified technically-qualified individual?

8.       If you ever experience significant alpha intakes at your nuclear plant 
that require you to perform in vitro bioassay (fecal and urine sampling), do 
you follow a set collection protocol for each sample type that is set up for 
being run by HP Techs without Staff HP or other technically-qualified 
individual input?

9.       Do you have separate protocols for fecal sampling and urine sampling?

10.   If you use urine sampling for in vitro, do you specify 24-hr urine or 
spot urine?

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