Accelerated carbonation and structural transformation of blast furnace slag by mechanochemical alkali-activation

Alternative cements and production routes are necessary to offset the considerable global CO2 emissions of Portland cement production. The combination of alkali-activation and mechanochemical milling in a CO2 rich atmosphere is a promising green direction for synthesizing cementitious material as it upcycles hazardous material (slag) while capturing wt% of CO2 during synthesis. We investigate the resulting structural transformations incurred during synthesis and hydration using a suite of characterization techniques including solid-state Al-27, Si-29, and C-13 NMR. The local aluminosilicate network structure of the processed clinker is best described by a melilite-type structure. Upon hydration, the network polymerizes to form a calcium, sodium aluminosilicate hydrate gel. The synthesis route also creates various metastable carbonates and bicarbonates from captured CO2 and alkali-additives that transform into stable carbonate phases like calcite, aragonite, and gaylussite, after hydration. This indicates accelerated carbonation reactions occur during clinker production and demonstrates novelty as a green cement technology.

Automated summary

The combination of alkali-activation and mechanochemical milling in a CO2 rich atmosphere for synthesizing cementitious materials shows promise in upcycling hazardous materials and capturing CO2. Structural transformations during synthesis and hydration were studied using solid-state Al-27, Si-29, and C-13 NMR techniques.