Hydroxide products, adsorption behavior

Alternatively, several workers have shown that not only is the soluble, zero-charged hydrolysis product considerably more surface active than the free (aquo) ion but also a polymeric charged or uncharged hydrolysis product may be formed at the solid-liquid interface at conditions well below saturation or precipitation in solution. Hall (5) has considered the coagulation of kaolinite by aluminum (III) and concluded that surface precipitates related to hydrated aluminum hydroxide control the adsorption-coagulation behavior. Similarly Healy and Jellett (6) have postulated that the polymeric, soluble, uncharged Zn(OH)2 polymer can be nucleated catalytically at ZnO-H20 interfaces and will flocculate the colloidal ZnO via a bridging mechanism. 

At the PWR primary coolant pH of 7 to 8, the fission product isotopes of the tri- and tetravalent elements show strong hydrolysis, resulting in very low solubilities. This macrochemical behavior is consistent with the observations made in coolant analyses that these radionuclides can be almost quantitatively isolated together with the suspended corrosion products by filtration. However, this behavior does not necessarily indicate the presence of particular oxides or hydroxides of these fission products, since due to their very low element concentrations in the coolant their solubility limits are probably not exceeded. Presumably, these element traces are attached to the corrosion product oxides either by adsorption onto their surfaces or by formation of mixed crystals. A significant fraction of the longer-lived tri- and tetravalent fission products, as well as of the actinides, is incorporated into the contamination layers which cover the primary circuit surfaces. However, because of the usually very low actiAuty concentrations of these radionuclides in the coolant and, consequently, in the contamination layers, their contribution to the contamination dose rates is negligible. 

---