Microstructure Evolution Mechanism of Geopolymers with Exposure to High-Temperature Environment

Abstract

The investigation on geopolymers has intrigued broad interests in the past decades, due to the requirements for the recycling of aluminosilicate solid wastes, such as red mud, slags, sludges and demolished concrete. Previous studies have demonstrated the feasibility of reusing this Aluminosilicate as a resource to prepare cementitious materials and indicated their promising properties at ambient temperature. However, when this material was exposed to high temperatures, especially above 1000 °C, the microstructure evolution mechanisms were not systematically investigated. In this study, the microstructural evolution process of metakaolin-based K geopolymer (molar ratio of K:Al:Si was 1:1:4) is investigated. The crystalized leucite originated from the geopolymer precursor was detected above 1000 °C. The SEM results indicate that the microstructure of the geopolymer before heating was composed of non-reacted metakaolin with a typical layered structure and reacted amorphous binder phase. As the geopolymer heated to 1000 °C, the microstructure of the geopolymer changed to a porous structure with an average pore size from 10 to 30 μm. When the heating temperature reached 1100 °C, the pores started to close along with the leucite crystallization process. As the heating temperature reached 1200 °C, most of the pores were closed. The TEM results show that the microstructure of the geopolymer, after being heated to 1400 °C, was composed of an amorphous glassy phase and crystallized leucite phase. The crystallized leucite grains originated from the nano-sized crystal nuclei, with an average size of 2–3 nm. The TEM-EDS results indicate that the chemical composition of the glassy phase was complicated. It varied from area to area because of the movement and uneven distribution of K.