This
study focuses on the investigation of potential calcium-based,
low-cost sorbent materials for post-combustion CO2 capture
via carbonate looping. Mineral limestone, carbide slag, and white
mud were evaluated for their CO2 sorption activity, with
the latter two being industrial wastes retrieved from chlor-alkali
and paper pulp plants, respectively. Mineral magnesite was tested
as a structural promoter in an attempt to improve the cyclic stability
of the sorbents. Different methods consisting of hydration, acetic
acid treatment, and a modified sol–gel autocombustion using
glycerol as the combustion agent were applied to modify the structural
and morphological characteristics of the mineral- and waste- derived
CaO and improve their performance. Preliminary thermogravimetric analysis
(TGA) tests proved the superiority of limestone and carbide slag treated
with glycerol autocombustion over white mud. The addition of magnesite
was considered more beneficial via the acetic acid treatment, since
the promoted limestone and carbide slag presented adequate stability
under 50 sorption/desorption TGA cycles, with a 43.2% and 34.2% deactivation,
respectively. The most promising CaO-based sorbents were further evaluated
in a bench-scale fluidized-bed reactor, with the promoted materials
withstanding sintering more distinctly, even under more severe calcination
conditions (880 °C, 50% CO2 concentration). Magnesite-promoted
limestone exhibited an initial CO2 uptake of ∼11
mol CO2/kg of sorbent, which corresponds to ∼90%
CaO conversion and <35% deactivation after 20 consecutive carbonation
cycles, even under harsh calcination conditions. The superiority of
the limestone promoted with magnesite was attributed to the enhancement
of its pore network due to a reconstruction of its morphology in the
presence of steam during the carbonation/calcination cycles.