North Anna's response is similar to San Onofre.  In addition, we utilize our 
waste stream analysis to calculate scaling factors to supplement bioassay gamma 
emitters, isotopic smear results, and air sample results.


Barbara J. Thompson
Supervisor of Exposure Control
Dominion - North  Anna Power Station
Email:  [email protected]
Phone:  540-894-2605
Beeper: #3469
FAX:  540-894-2408



From: [email protected] [mailto:[email protected]] On Behalf Of 
[email protected]
Sent: Thursday, September 30, 2010 7:03 PM
To: [email protected]
Cc: [email protected]; [email protected]
Subject: Re: Powernet: In Vivo and In Vitro Counting Protocols

Greg,

As background, INPO recommends internal dose assessment at about the same level 
that external dose is monitored (10 mrem).  EPRI Alpha guidelines recommends 
the alpha component be included in an dose assessment if an intake is likely to 
exceed 10 mrem CEDE.  The EPRI guidelines describe whole body counting for 
gamma emitters and scaling factors for non-gamma emitters  as the most accurate 
method of internal dose assessment.  Scaling factors are normally based on the 
ratio of cobalt-58/60 and gross alpha activity from a representative air 
sample.  A representative smear may be substituted if an appropriate air 
samples is not available.  The EPRI guideline recommends that bioassay be 
considered if an intake is likely to exceed 5% ALI (250 mrem CEDE).  It's 
expected that sampling containers be available and that a contract for sample 
analysis be in place.

It is very unlikely that the 5% ALI level be reached.  When establishing a 
station practice for sampling at a lower level, the negative impact of sample 
collection on a radiation worker and family should be considered.  Since these 
events rare, each is handled on a case-by-case basis by the radiation safety 
technical staff.  In one case at San Onofre, 24 hour urine was collected.

Best regard,
Mike








To: "[email protected]" <[email protected]>
From: "GOWDY, GREGORY M" <[email protected]>
Sent by: [email protected]
Date: 09/22/2010 06:54PM
Subject: Powernet: In Vivo and In Vitro Counting Protocols

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.

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?

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?

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

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




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