Effect of natural carbonation on the pore structure and elastic modulus of the alkali-activated fly ash and slag pastes

Abstract

The aim of this paper was to investigate the effect of natural carbonation on the pore structure, and elastic modulus (E_m) of alkali-activated fly ash (FA) and ground granulated blast furnace slag (GBFS) pastes after one year of exposure in the natural laboratory conditions. The chemical changes due to carbonation were examined by X-ray diffraction (XRD), scanning electron microscope/energy-dispersive X-ray (SEM−EDX) and attenuated total reflectance Fourier transformed infrared spectroscopy (ATR-FTIR). Subsequently, the pore structure and E_m of the degraded material were tested by mercury intrusion porosimetry (MIP), nitrogen (N₂) adsorption, and nanoindentation. The chemical degradation of alkali-activated pastes due to natural carbonation is showed to be dependent on the GBFS content and their pore structure development. It was found that the pure alkali-activated GBFS paste was not carbonated at all within the tested period due to fine gel pore structure. On the other hand, carbonation of the gel in the pastes consisting FA and GBFS generated significant mineralogical and microstructural changes. The extensive decalcification of the gel was reflected in the increase of nanoporosity. Consequently, the E_m of the carbonated pastes decreased. This study suggests that the degradation of alkali-activated FA and GBFS pastes due to carbonation may be accurately evaluated through micromechanical properties measurements rather than only by testing alkalinity of the pore solution and corrosion of reinforcement such as commonly studied carbonation effect in the ordinary Portland cement (OPC)-based materials.