134 Cs and 137 Cs activity ratios give roughly 1066 times higher activity in the leaked water than the reported tank measurement. Elevated activity of water leaked from tank 5 might be due to radionuclides adsorbed on sediment particles. Adsorption by cation-exchange in NaCl dominated solutions is more, or less inversely proportional to pH.
134 Cs and 137 Cs activity ratios give roughly 1066 times higher activity in the leaked water than the reported tank measurement. Elevated activity of water leaked from tank 5 might be due to radionuclides adsorbed on sediment particles. Adsorption by cation-exchange in NaCl dominated solutions is more, or less inversely proportional to pH.
134 Cs and 137 Cs activity ratios give roughly 1066 times higher activity in the leaked water than the reported tank measurement. Elevated activity of water leaked from tank 5 might be due to radionuclides adsorbed on sediment particles. Adsorption by cation-exchange in NaCl dominated solutions is more, or less inversely proportional to pH.
James Crawford, Kemakta Konsult AB, Stockholm, Sweden
From Tepcos homepage we have the following reported measurement data:
134 Cs 137 Cs Cl Ref. Leak water 4.610 4 Bq/L 1.010 5 Bq/L 5 200 mg/L http://bit.ly/157KhyS Tank 5/H4 water 4.410 1 Bq/L 9.210 1 Bq/L 5 200 mg/L http://bit.ly/15zZtbo ratio (Leak/Tank) 1046 1086 1 Taking the average of 134 Cs and 137 Cs activity ratios gives roughly 1066 times higher activity in the leaked water than the reported tank measurement. The same Cl concentration reported in both samples implies that the elevated activity of the leak water is not due to evaporation. It is possible that the elevated activity of water leaked from Tank 5 might be due to radionuclides adsorbed on sediment particles. The measured Cl concentration also implies water roughly 7 times more dilute than an average seawater. If the activity of the leaked water (C total ) is taken to be equal to the sum of dissolved activity (C w ) plus that sorbed on sediment particles (C s ), the mass of sediment per volume of water can be estimated from an activity balance if the partitioning coefficient (K d ) is known for the nuclide in question. The K d is the ratio of adsorbed activity divided by dissolved activity (C s /C w ) at equilibrium, and typically given in units of m 3 /kg (or g/L). In the absence of any additional information it must also be assumed that the activity measured in the tank is representative of sediment free water and the same as the dissolved activity in the leak water. An adsorbent material apparently being used at the cleanup site is IONSIV R9120-B zeolite (http://bit.ly/15mvgcx) which has a reported K d for Cs of ~10 000 m 3 /kg at pH 7.5 in water with salinity (as far as I can tell) of seawater. Adsorption by cation-exchange in NaCl dominated solutions is more, or less inversely proportional to the dissolved Na + concentration. The K d in the diluted seawater should therefore be about 7 times greater, or roughly 70 000 m 3 /kg assuming Na + is dominant cation (all other things being equal). For comparison, a natural geological adsorbent such as bentonite clay (Na-Montmorillonite) has a K d not much greater than about 0.12 m 3 /kg for roughly the same water composition (http://bit.ly/1fuJxJb). The specific mass of sediment per volume of water, m/V (kg/m 3 ) can be calculated from the activity balance: 1 total s w d d w w C C C m m K K C C V V + | | = = + ~ | \ .
From this formula, a C total /C w ratio of ~1066 is consistent with an m/V ratio of 0.15 g/L for the IONSIV adsorbent. If the sediment were a natural geological material like clay (bentonite), we would probably need in excess of 8 kg/L to get the same total activity (i.e. not a realistic amount). The elevated activity of the leak water therefore seems like it could be due to the presence of a small amount of the zeolite adsorbent (equivalent to a fraction of a teaspoon per L) although probably not a natural geological material.