Modeling Atmospheric Releases of Molecular Tritium 2005 RETS/REMP Workshop Jim Key Key Solutions, Inc. www.keysolutionsinc.com.

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Transcript Modeling Atmospheric Releases of Molecular Tritium 2005 RETS/REMP Workshop Jim Key Key Solutions, Inc. www.keysolutionsinc.com.

Modeling Atmospheric Releases
of Molecular Tritium
2005 RETS/REMP Workshop
Jim Key
Key Solutions, Inc.
www.keysolutionsinc.com
Tritium Woes
• Keep It?
– High Plant Inventories
– Worker Exposure Problem
– Increased Risk of Adverse
Environmental Impact from
Accidental Releases of
High Concentrations
TRITIUM
Tritium Woes
• Release It?
– Via Liquid Effluents?
• Lowest Dose Impact
• High Political Impact for Some Sites
– Via Gaseous Effluents?
• Higher Dose Impact
• Not ALARA
Dosimetric Impact of Liquid vs.
Gaseous Releases of HTO
• Reg. Guide 1.109 and NUREG 0133
Models Indicate Significant Increase in
HTO Dose for Atmospheric vs. Liquid
Releases
• Exact Dose Increase is Site Specific but
Typically 10 Times or Greater
• Significant Risk of Site Contamination
(condensation on build surfaces, etc.)
A Different Idea
• Why Not Release to Atmosphere as
HT?
• Significantly Lower Dose Impact
• Canadian Technology – Electrolytic
Decomposition of HTO to HT and O2
• Canadians Release ~ 10 x More
Tritium to Environment than U.S.
Dosimetric Impact
of HT vs. HTO
• Radiotoxicity of HTO ~ 20,000-25,000
Times that of HT (ICRP-30)
• Only Significant Dose Impact Occurs
Following Oxidation of HT to HTO and
Subsequent Exposure
Why Model Molecular Tritium?
• Need Ability to Predict Environmental
Concentrations for Decision Making.
• If Tritium is Released Atmospherically as
HT, then ODCM Must be Revised to Model
Doses.
• Reg. Guide 1.109 and NUREG 0133
Assume Tritium Released in the Form of
Tritiated Water – HTO
Field Studies of Atmospheric
HT Releases
• AECL – Chalk River Laboratory, Canada
– 1986 – 18.5 Ci of HT Released
– Pure HT Release
• Savannah River Site, USA
– 1974 – 479,000 Ci of HT Released
– 1975 – 182,000 Ci of HT Released
– Estimated 99% HT, 1% HTO
• Short Term Releases
BIOMASS-3
• IAEA Tritium Working Group Report 2003 - “Modeling the Environmental
Transport of Tritium in the Vicinity of Long
Term Atmospheric and Sub-Surface
Sources”
• Provides Comparison of Numerous Tritium
Models Against Field Measurements
BIOMASS-3
• Models Atmospheric Releases of Molecular
Tritium (HT) as well as Tritiated Water
(HTO)
• These are all screening models and as such
result in very conservative estimates of
Tritium exposure.
BIOMASS-3
Examines Models Used By:
•
•
•
•
•
•
AECL – Canada
BEAK – Canada
ANDRA – France
CEA – France
FZK – Germany
ZSR – Germany
•
•
•
•
•
JAERI – Japan
NIPNE – Romania
VNIIEF – Russia
SESAB – Sweden
LLNL – USA
Oxidation of HT to HTO
• Oxidation in
Atmosphere is Very
Slow Process with
Half Life of > 5
Years
• Most Significant
Oxidation Occurs at
the Atmosphere-Soil
Interface
HT
HTO
Oxidation of HT to HTO in Soil
• Result of Bacterial Action in Soil
• Oxidation Efficiency is Highly Dependant
on Organic Content of Soil
– Sterilized Clay Loam ~ 3.4%
– Natural Clay Loam
100%
• Occurs Very Quickly ~ hours
Oxidation of HT in Soil
• Described by “Deposition Velocity” - Vd
• Typical Values: 0.00003 to .00034 m/sec
• Allows Determination of Ground Plane
Concentration (activity/m2) of HTO
Resulting from Oxidation of HT
Atmospheric Dispersion of HT
• HT Has Approximately 6% Density of Air
• Might Seem that HT Would Quickly Diffuse
Out of Plume
• Field Studies Have Shown that HT Remains
Entrapped in Plume in the Near Field
• BIOMASS-3 Models All Model HT
Dispersion Using Standard Gaussian Plume
Model
Effective Ground Plane Deposition


 Q sec m  V
3
HT
d
m sec  D Q1 m 
2
Effective Ground Plane Deposition Rate
 Ci / m 2 
DepHTO 

 sec 
 sec 
 Ci 
HT  m 

  Q  3   Vd    Q HT  
m 
 sec 
 sec 
Physical Transport
Pathways Considered
• Soil Moisture
– Deposition of HT onto ground plane with
subsequent oxidation to HTO.
• Airborne Concentration from Soil
Re-Emission
– Emission of HTO (oxidized HT) into air from
soil moisture.
Methodology Development
• Special Thanks to Ring Peterson at LLNL
– NEWTRIT Model Described in HPS Journal,
Feb. 2002.
• Screening Model – Unrealistically Conservative
– DCART Model (unpublished internal LLNL
report, Sept. 2004).
• Incomplete Model But Rather a General Approach
• More Realistic Assumptions
Methodology Development
• Methodology Presented Here Makes Use of
DCART Strategy for Predicting
Environmental Concentrations of HTO Due
to Atmospheric Releases of HT
• Methodology Designed to be Compatible
with Reg Guide 1.109 and NUREG 0133
Approaches
• Easily Incorporated into Current ODCM
Methodology
Soil Moisture Concentration
CSM ,dep
Where:
CSW,dep
3.15104
fr

Q
HT
Precip

 Q Q
 3.1510  f 
4
Vd
Precip
HT
r
annual mean concentration of HTO in soil water
deposition of HT.
is 3.15107 sec/yr  10-3 m3/L.
fraction of HTO retained in soil for plant root
uptake (0.3).
annual release rate of HT.
annual precipitation [m/yr].
Airborne Concentration Due to
Re-Emission
• Described in terms of HTO in air to HT in air
based on field measurements.
• Specified in units of m3/L (e.g. pCi/L of HTO in
air to pCi/m3 of HT in air)
– Note must multiply by:

AbsoluteHumidity kg m3
WaterDensitykg L
to get pCi/m3 HTO in air

Airborne Concentration Due to
Re-Emission
Defined for two heights above soil surface:
– grVeg
– grInh
20 cm for vegetation uptake
- typical value ~ 6 m3/L
1.5 m for inhalation exposure
- typical value ~ 4 m3/L
Airborne Concentration Due to
Re-Emission – Plant Exposure
CRair
Where:
CR-air
grVeg
HA
Water
 
Veg

  Q QHT  g r  HA Water
concentration of HTO in air due to re-emission of HTO
in soil.
concentration ratio of HTO in air to HT in air at height of
vegetation (20 cm) [m3/L].
absolute atmospheric humidity [kg/m3].
density of water [kg/L]
Concentration in Vegetation
C Veg


 Q Q

HT

 HR g

 HA
Veg
r
Where:
0.75
0.75
f r Vd 
 3.1510 1  H R 

P r ecip 
4
fraction of vegetation what is water [L/Kg].

ratio of vapor pressure of HTO and H2O (1.1).
HR
relative humidity.
Airborne Concentration Due to ReEmission – Inhalation Exposure
C
Inhal
R air
 
HA
Inh

  Q Q HT  g r 
 Water
Where:
CInhal
R air
airborne concentration of HTO in air at 1.5 m due to
re-emission from soil.
grInh
concentration ratio of HTO in air to HT in air due to
re-emission.
Dose Comparison Scenario
/Q =
Q
HA
HR
Precipitation
=
=
=
=
110-6 sec/m3
1000 Ci/yr
8 gm/m3
70%
30 inches/yr
HTO vs. HT Predicted Dose
Dose (mrem)
Pathway
HTO
HT
Inhalation
0.036
0.001
Vegetation
0.157
0.012
Cow Milk
0.050
0.004
Goat Milk
0.136
0.010
Total
0.328
0.023
Liquid Release of HTO of
Atmospheric Release of HT?
• Both Appear to Have the Same Dose Impact
• Exact Comparison Requires Site Specific
Analysis
• Obviously Is Not Cost Beneficial If Liquid
Discharge is an Option
• Possible Option Where Liquid Releases Are
Not Viable