C–(N)–S–H and N–A–S–H gels: Compositions and solubility data at 25°C and 50°C. Issue 6 (25th March 2017)

• Record Type: Journal Article
• Authors: Gomez‐Zamorano, Lauren; Balonis, Magdalena; Erdemli, Bartu; Neithalath, Narayanan; Sant, Gaurav
• Is Part Of: Journal of the American Ceramic Society. Volume 100:Issue 6(2017)
• Page Start: 2700
• Page End: 2711
• Publication Date: 2017-03-25
• Subjects: calcium silicate hydrate -- cements -- geopolymers -- solubility -- thermodynamics; Ceramics -- Periodicals; 620.1405
• DOI: 10.1111/jace.14715
• Languages: English
• ISSNs: 0002-7820

Abstract

Abstract: Calcium silicate hydrates containing sodium [C–(N)–S–H], and sodium aluminosilicate hydrates [N–A–S–H] are the dominant reaction products that are formed following reaction between a solid aluminosilicate precursor (eg, slags, fly ash, metakaolin) and an alkaline activation agent (eg NaOH) in the presence of water. To gain insights into the thermochemical properties of such compounds, C–(N)–S–H and N–A–S–H gels were synthesized with compositions: 0.8≤Ca/Si≤1.2 for the former, and 0.25≤Al/Si≤0.50 (atomic units) for the latter. The gels were characterized using thermogravimetric analysis (TGA), scanning electron microscopy with energy‐dispersive X‐ray microanalysis (SEM‐EDS), and X‐ray diffraction (XRD). The solubility products (KS 0 ) of the gels were established at 25°C and 50°C. Self‐consistent solubility data of this nature are key inputs required for calculation of mass and volume balances in alkali‐activated binders (AABs), and to determine the impacts of the precursor chemistry on the hydrated phase distributions; in which, C–(N)–S–H and N–A–S–H compounds dominate the hydrated phase assemblages.