Investigation of the viscoelastic evolution of reactive magnesia cement pastes with accelerated hydration mechanisms

Viscoelasticity of reactive magnesia cement (RMC) pastes containing 3 different hydration agents (HCl, Mg (CH3COO)2 and MgCl2) were investigated. Amplitude sweep, frequency sweep and time sweep of RMC pastes were examined within 3 h of hydration. Time-dependent evolution of storage modulus, loss modulus, phase angle, and shear stress were recorded. Measurements of pH, isothermal calorimetry, XRD, TG-DTG and FTIR were used to analyze hydration reaction and products. Addition of hydration agents (HAs) accelerated the growth rate of storage modulus/loss modulus over time. MgCl2 demonstrated the greatest acceleration influence, also reflected in non-destructive structural build-up and buildability related to 3D printing applications. Addition of MgCl2 and HCl advanced the initial setting time of RMC pastes to 100-110 min, during which yield stress reached maximum, and decreased afterwards. Within 3 h of hydration, pastes containing MgCl2 revealed lowest pH, highest heat release and brucite concentration. HAs inclusion precipitated brucite away from MgO particles in the bulk solution, creating a bridge between MgO particles and enabling denser microscopic network structure.