Duolite™ GT-73 ion exchange resin routinely reduces the mercury content of a waste water stream to less than the permitted level of 10 ppb. Effluent concentrations from the ion exchange facility (IEF) are consistently between 1 to 5 ppb, even though the feed contains a varying concentration of mercury (0.2 to 70 ppm). Two operational problems have been encountered at that facility, however. Firstly, the stated capacity of the resin for mercury was not being achieved. The abnormally low capacity was traced to analytical laboratory waste which was intermittently treated by the resin. That waste contained hydrochloric acid, stannous chloride, and potassium permanganate, among other chemicals, which presumably eluted sorbed mercury from the resin and also oxidized the thiol (SH) functional groups on the resin and rendered them inactive. The net effect was that the resin had to be replaced more frequently than anticipated. Secondly, the IEF was temporarily shut down because the mercury content of the waste water could not be reduced to below the permitted level, even with fresh resin. That problem was caused by slow settling solids composed mainly of iron which apparently adsorbed some of the mercury and allowed it to pass through the resin untreated. The solids were presumably a result of processing waste water abnormally high in iron which may have co-precipitated with mercury and other elements in the feed and caused a residual buildup of solids throughout the IEF. The problem was remedied by installing a 0.2 µm cartridge filter between the feed tank and the columns.
A systematic model-based approach is used for development of an
efficient carousel ion-exchange
process for the selective removal of radioactive
137Cs+ from alkaline nuclear waste
solutions.
Equilibrium data for two resorcinol−formaldehyde (R−F)
cation-exchange resins are correlated
by an empirical equation of the Freundlich−Langmuir type over
cesium/sodium concentration
ratios of 10-9 to
10-2 and sodium concentrations of 1 to 6 N.
The standard deviations are 3.5
and 6.6%, respectively. The data cannot be accurately described
by mass action equations. A
detailed rate model, developed in this study for the periodic
countercurrent multicolumn operation
of carousel systems, is used with the equilibrium correlations to
simulate cesium breakthrough
curves from R−F resin columns. Results show that accuracy of the
predicted breakthrough
curves are directly related to the accuracy of the isotherm data and
correlations. Cesium
breakthrough position is generally predicted to within 5% or less for
10 of 13 runs over linear
superficial velocities of 0.16 to 8.8 cm/min, column lengths of 3.14 to
118.5 cm, and particle
radii of 145 to 200 μm. One run shows later breakthrough than
predicted as a result of a low
potassium concentration in the feed. Two other runs show early
breakthroughs as a result of
channeling in poorly packed columns of a carousel system. Despite
the channeling, strong
thermodynamic self-sharpening effects helped establish constant pattern
waves in the downstream columns. A case study for a pilot-scale carousel unit shows
that 100% utilization of
cesium capacity and maximum throughput can be achieved while containing
the mass transfer
zone within the downstream columns. Since intraparticle diffusion
controls spreading of the
breakthrough curves, reducing the particle radius from 200 to 145 μm
increases throughput by
40%.
When immobilizing into borosilicate glass the radionuclides in the caustic high-level radioactive wastes stored in the USA, the soluble fission product Cs-137 has to be removed from supernates of the wastes. In the current processes zeolites or an organic precipitant will be used to remove the Cs. These are then treated further and mixed with the radioactive sludges and vitrified into a borosilicate glass. This paper describes the vitrification of a mixture resulting from using a new process to remove Cs from the caustic supernate. A resorcinol based organic ion exchange resin is used. This resin was then mixed with sludge and frit and vitrified. Using an organic ion exchange resin rather than zeolite or the organic precipitant has certain advantages. For example, use of the zeolite increases the amount of glass to be made and use of the organic precipitant produces benzene as a secondary waste stream. Results in the paper indicate that a mixture of the resin, sludge and frit can be successfully vitrified in a joule-heated, slurry fed melter. However, when resin is present in the feed, the glass becomes less durable due to the increased amount of Fe(II) caused by reduction of Fe(III) in the melt. Based on the durabilities of other waste glasses, this glass is still suitable as a canistered wasteform.
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