Compositions and Microstructures of Carbonated Geopolymers with Different Precursors

Abstract

It is thought that geopolymers are easy to carbonate, especially when they are cured in ambient temperatures. Matrix gel’s composition and microstructure, and new products of geopolymers (GPs) after carbonation were investigated in this study on the basis of XRD and SEM-EDS measurements and ternary diagram analysis, which were prepared from low-lime fly ash (FA) and ground granulated blast-furnace slag (GGBS) alone or a blend, as a precursor. The specimens were hardened in a 20 °C environment with alkali activator solution (S/N = 1.1 in mole), followed by storage under sealing or accelerated carbonation. XRD patterns show that carbonation products were nahcolite for the sole FA-based GP and calcite for the GPs using GGBS alone or as a blend. The SEM images of carbonated samples show that there were cube-shaped calcite and small calcite particles in the GGBS-based GP, but hail-like particles in the FA/GGBS blend-based GP. The hail-like particles were complexes of calcite and C-A-S-H gels determined by ternary diagram analysis, and were found to plug the top of the pores of the spongy C-A-S-H gels. We also confirmed that combined ternary diagram analysis of S-(C + M + N)-A and A-(C + M)-N are very effective in determining the gel type of a geopolymer, as well as the products and compositional changes after carbonation, in which oxide components of gels are determined by SEM-EDS. In the former diagram, C-A-S-H gels were plotted linearly along the (C + M + N)-albite (Ab) join, while N-A-S-H gels showed a scattered distribution. In the latter diagram, the plots for N-A-S-H and C-A-S-H gels are distributed in different zones. N = Na2O, C = CaO, M = MgO, A = Al2O3, S = SiO2, H = H2O.