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DOE/ORO/2327 Oak Ridge Reservation Annual Site Environmental ...

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<strong>Oak</strong> <strong>Ridge</strong> <strong>Reservation</strong><br />

The charcoal cartridges, particulate filters, and silica-gel traps are collected weekly to biweekly. The<br />

use of charcoal cartridges is a standard method for capturing and quantifying radioactive iodine in<br />

airborne emissions. Gamma spectrometric analysis of the charcoal samples quantifies the adsorbable<br />

gases. Analyses are performed weekly to biweekly. Particulate filters are held for 8 days prior to a weekly<br />

gross alpha and gross beta analysis to minimize the contribution from short-lived isotopes such as 220 Rn<br />

and its daughter products. At Stack 7911, a weekly gamma scan is conducted to better detect short-lived<br />

gamma isotopes. The filters are then composited quarterly and are analyzed for alpha-, beta-, and gammaemitting<br />

isotopes. At Stack 7880, the filters are composited monthly and analyzed for alpha-, beta-, and<br />

gamma-emitting isotopes. The sampling system on Stack 7880 requires no other type of radionuclide<br />

collection media. Compositing provides a better opportunity for quantification of the low-concentration<br />

isotopes. Silica-gel traps are used to capture water vapor that may contain tritium. Analysis is performed<br />

weekly to biweekly. At the end of the year, the sample probes for all of the stacks are rinsed, except for<br />

8915 and 7880, and the rinsate is collected and submitted for isotopic analysis identical to that performed<br />

on the particulate filters. A probe-cleaning program has been determined unnecessary for 8915 because<br />

the sample probe is a scintillator probe used to detect radiation and not to extract a sample of stack<br />

exhaust emissions. It is not anticipated that contaminant deposits would collect on the scintillator probe.<br />

A probe-cleaning program for 7880 has established that rinse analysis has historically shown no<br />

detectable contamination. Therefore, the frequency of probe rinse collection and analysis is no more often<br />

than annually.<br />

The data from the charcoal cartridges, silica gel, probe wash, and the filter composites are compiled<br />

to give the annual emissions for each major source and some minor sources.<br />

5.4.3.2 Results<br />

<strong>Annual</strong> radioactive airborne emissions for ORNL in 2009 are presented in Table 5.12. All data<br />

presented were determined to be statistically different from zero at the 95% confidence level. Any number<br />

not statistically different from zero was not included in the emission calculation. Because measuring a<br />

radionuclide requires counting random radioactive emissions from a sample, the same result may not be<br />

obtained if the sample is analyzed repeatedly. This deviation is referred to as the “counting uncertainty.”<br />

Statistical significance at the 95% confidence level means that there is a 5% chance that the results could<br />

be erroneous.<br />

Historical trends for tritium and 131 I are presented in Figs. 5.13 and 5.14, respectively. The tritium<br />

emissions for 2009 totaled approximately 163.9 Ci (Fig. 5.13), which is an increase from 2008. The 131 I<br />

emissions for 2009 totaled 0.17 Ci (Fig. 5.14), which is a significant increase from the past 5 years.<br />

Increases in 131 I emissions were due to [Please see Pat Scofield].<br />

For 2009, the major offsite dose contributors at ORNL were 138 Cs, 212 Pb, and 41 Ar with dose<br />

contributions of approximately 34%, 32%, and 11%, respectively. Emissions of 41 Ar result from HFIR<br />

operations and research activities and are emitted as a nonadsorbable gas from the 7911 Melton Valley<br />

complex stack. Emissions of 138 Cs result from research activities in the Radiochemical Engineering<br />

Development Center, which also exhausts through the 7911 Melton Valley complex stack. Emissions of<br />

212 Pb result from the radiation decay of legacy material stored onsite and contamination areas containing<br />

isotopes of 228 Th, 232 Th, and 232 U. Emissions of 212 Pb were emitted from the following stacks: 2026, 3020,<br />

3039, 7503, 7856, 7877, 7911, and the Sewage Treatment Plant (STP) Sludge Drier (Fig. 5.15). The<br />

calculated radiation dose to the maximally exposed off-site individual from all radiological airborne<br />

release points at ORNL during 2009 was 0.3 mrem. This dose is well below the NESHAP standard of<br />

10 mrem and is less than 0.10 % of the 300 mrem that the average individual receives from natural<br />

sources of radiation. (See Sect. 7.1.2.1 for an explanation of how the airborne radionuclide dose was<br />

determined.)<br />

5-32 <strong>Oak</strong> <strong>Ridge</strong> National Laboratory

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