Cement and Concrete Research, Volume 54, 2013, Pages 143-150.
N. Jambunathan, J.G. Sanjayan, Z. Pan, G. Li, Y. Liu, A.H. Korayem, W.H. Duan, F. Collins.
Department of Civil Engineering, Monash University, Clayton, Victoria 3800, Australia and
Faculty of Engineering & Industrial Sciences, Swinburne University of Technology, Hawthorn, Victoria, Australia and
School of Mechanical and Chemical Engineering, The University of Western Australia, Crawley, WA 6009, Australia and
School of Geosciences and Info-Physics, Central South University, Changsha 410083, China.
Abstract
The strength and microstructural evolution of two alkali-activated slags, with distinct alumina content, exposed to 50 °C have been investigated. These two slags are ground-granulated blast furnace slag (containing 13% (wt.) alumina) and phosphorous slag (containing 3% (wt.) alumina). They were hydrated in the presence of a combination of sodium hydroxide and sodium silicate solution at different ratios. The microstructure of the resultant slag pastes was assessed by X-ray diffraction, differential thermogravimetric analysis, and scanning electron microscopy. The results obtained from these techniques reveal the presence of hexagonal hydrates: CAH10 and C4AH13 in all alkali-activated ground-granulated blast-furnace slag pastes (AAGBS). These hydrates are not observed in pastes formed by alkali-activated ground phosphorous slag (AAGPS). Upon exposure to 50 °C, the aforementioned hydration products of AAGBS pastes convert to C3AH6, leading to a rapid deterioration in the strength of the paste. In contrast, no strength loss was detected in AAGPS pastes following exposure to 50 °C.