Xiaoyun Du, Zhiyuan Shao, Jun Chang, Kai Cui
Limestone calcined clay cement (LC 3 ) is widely recognized as a sustainable cementitious material. However, the low reactivity of natural limestone often limits the early carbon aluminate reaction and compromises the early compressive strength of LC 3 . This study proposes the preparation of highly active CaCO 3 by carbonating SS, RCP, MS, and CS. The resulting product is then used to replace limestone and activate early carbon aluminate reactions in LC 3 . This strategy aims to develop a sustainable engineering material with high compressive strength and low CO 2 emissions, referred to as carbonated waste calcined clay cement (CWC 3 ). The results showed that compared with LC 3, the compressive strength of CWC 3 at 3 and 28 days increased by 19.7% and 10.8%, respectively, while the CO 2 emissions and CO 2 index decreased by 14.4% and 21.9%, respectively. The mechanism of early activation of the CWC 3 carbon aluminate reaction includes two aspects: the crystallite grain size and crystallinity of CaCO 3 in carbonated waste are much smaller and lower than those of CaCO 3 in natural limestone with a polycrystalline crystal cluster morphology. This structure introduces a higher density of crystal defects, thereby enhancing chemical reactivity. CaCO 3 crystal clusters and silica gel are interlaced in a carbonated waste particle, and the volcanic ash reaction of silica gel disperses the CaCO 3 crystal clusters, thereby inducing more carbon aluminate reaction interfaces. In addition, the nucleation of highly active CaCO 3 accelerates the hydration kinetics of CWC 3, generating more hydration products (such as Hc, Mc, and Ms), inducing denser pores, and ultimately contributing to the improved compressive strength. The carbonated waste exhibits the highest CO 2 sequestration amount of 513.4 g/kg, underscoring the significant environmental sustainability of CWC 3 .