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International Slag Valorisation SymposiumLeuven6-7/4/2009 - Third ...

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leaching (mg/kg dry matt er)<br />

3.0<br />

2.5<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

0.0<br />

0 25 50 75 100 125 150 175<br />

carbonation time (h)<br />

1 st <strong>International</strong> <strong>Slag</strong> <strong>Valorisation</strong> Symposium│Leuven│6-7/4/<strong>2009</strong><br />

Sb<br />

3.5<br />

3.0<br />

2.5<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

0.0<br />

Cu<br />

0 25 50 75 100 125 150 175<br />

carbonation time (h)<br />

Figure 7: Leaching of antimony and copper as a function of carbonation time. The<br />

different data points at the same carbonation time indicate different processing<br />

conditions (temperature, CO 2 concentration, moisture content).<br />

In blended waste-cement monoliths the carbonate introduction and pH decrease become<br />

decoupled. 6,9) Because of the presence of Calcium-Silicate-Hydrate, a key component in<br />

hydrated cement with a high pH buffering capacity, progressive carbonation first<br />

introduces carbonate in the pore water without decreasing pH. As a result, calcium<br />

leaching decreases. Only at a more advanced stage of carbonation does the pH decrease<br />

and carbonates are converted into bicarbonates, the salts of which are highly soluble.<br />

Therefore, calcium leaching from almost completely carbonated with mildly acidic<br />

leachant is higher than leaching from partially carbonated samples. Metals for which the<br />

carbonate salt is more soluble than the hydroxide go through a different scheme. Lead,<br />

for example, is soluble at high pH as a lead hydroxide complex. The very limited pH<br />

decrease in the first stage of carbonation shifts the equilibrium to the precipitated lead<br />

hydroxide, thus lowering lead leaching. With more advanced carbonation and<br />

significantly decreasing pH, lead hydroxide is converted into the soluble lead<br />

bicarbonate salt, thereby increasing lead leaching again.<br />

Besides the effects on mineral speciation and pH, carbonation also affects porosity.<br />

Carbonation leads to an average decrease of porosity and a modified particle size<br />

distribution. 10) In blended waste-cement mortars it was found that the relative<br />

importance of small capillary pores ( 0.1 µm) increases. The effect of carbonation-induced porosity<br />

decrease on leaching was shown to be significant for pH independent components such<br />

as sodium and, to a lesser extent, potassium. However, for heavy metals the pH effect of<br />

carbonation will be much more important.<br />

With these studies, significant insights have been gained on the carbonation reaction<br />

mechanism in different materials such as lime mortars, lime-based hydraulic mortars,<br />

alkaline wastes and waste-cement blends. It has been confirmed that the role of water is<br />

one of the key parameters in the carbonation process in a porous system, which requires<br />

leaching (mg/kg dry mat ter)<br />

34

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