The
present study investigates the carbonation of slags activated
by NaOH, Na2SiO3, Na2CO3, and Na2SO4. The main hydrates in those activated
with NaOH or Na2SiO3 were C-(N-)A-S-H, strätlingite,
and MgAl-layered double hydroxide phases as observed using different
experimental characterization techniques and thermodynamic modeling.
The use of a Na2CO3 activator led to the formation
of calcium carbonate and monocarbonate instead of strätlingite,
and Na2SO4 to ettringite formation. Carbonation
of the alkali-activated slags in a powdered form at 1 vol % concentration
of the CO2 environment proceeded rapidly, while little
change was observed after 7 d. The main carbonation products commonly
identified were calcium carbonate, carbonate containing-MgAl-layered
double hydroxide, and N-A-S-H. In Na2SiO3- and
Na2SO4-activated slags, M-S-H formation was
predicted, which destabilized the MgAl-layered double hydroxide phases.
Strätlingite and monocarbonate, which were initially present
or formed as a transient phase, were transformed to N-A-S-H during
carbonation, while C-(N-)A-S-H was only partially decalcified and
destabilized.