Abstract
Although faster transport velocities of colloid-associated actinides, bacteria, and virus than nonreactive solutes have been observed in laboratory and field experiments, some questions still need to be answered. To accurately determine the relative velocity (UPu/UT) of 239Pu and tritium representative of the bulk water, a conceptual model of electrostatic interactions coupled with the parabolic water velocity profile in pore channels is developed. Based on the expression for UPu/UT derived from this model, we study the effects of water flow rates and ionic strengths on the UPu/UT. Also, the velocity relationship between Pu, tritium and Sr2+ is explored. The results show that UPu/UT increased fairly linearly with decreasing water flow rates; UPu/UT declined approximately exponentially with increasing Na+ concentrations; the charge properties of colloid-associated Pu (negative), tritium (neutral) and Sr2+ (positive) had a close association with their transport velocities as UPu : UT : USr2+ = 1.41 : 1 : 0.579.
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