Martynas Statkauskas, Danutė Vaičiukynienė, Audrius Grinys, Laura Vitola
The cement industry is a major source of global CO2 emissions, driving the development of low-carbon alternatives such as geopolymers. This study examines geopolymer binders produced from ceramic brick waste (CBW) and metakaolin waste (MKW), evaluating their fresh and hardened properties as well as their performance under elevated temperatures. Five binder compositions were formulated by progressively replacing CBW with MKW (25-100 wt.%). The alkaline activator ratio (Na2SiO3/NaOH = 1.5) and NaOH molality (8 M) were kept constant. Fresh-state behavior was evaluated using Suttard viscometry and Vicat testing, while hardened-state performance was assessed through compressive and flexural strength, softening coefficient, and drying shrinkage. Thermal resistance was examined at 200, 400, 600, and 800 °C, supported by XRD, FT IR, and SEM analyses. The present study investigates how waste-derived aluminosilicate precursors with differing crystallinity and reactivity affect geopolymerization mechanisms and high-temperature phase evolution. MKW-rich binders were found to form highly reactive amorphous gels, resulting in superior early mechanical strength, whereas CBW-rich binders retained thermally stable crystalline phases that enhanced resistance to structural degradation at elevated temperatures. The MKW-rich formulation (F5) demonstrated the highest ambient mechanical performance, reaching 82.8 MPa after curing at 200 °C, due to intensified secondary geopolymerization. In contrast, the CBW-only binder (F1) exhibited superior thermal stability, maintaining a compressive strength of 46.4 MPa even after exposure to 800 °C. These findings establish a clear structure-property relationship between precursor mineralogy, gel chemistry, and high-temperature performance, offering valuable insights for the tailored design of waste-derived geopolymers with optimized thermal and mechanical properties.