Synchrotron X-ray nanotomographic and spectromicroscopic study of the tricalcium aluminate hydration in the presence of gypsum. (September 2018)

• Record Type: Journal Article
• Authors: Geng, Guoqing; Myers, Rupert J.; Yu, Young-Sang; Shapiro, David A.; Winarski, Robert; Levitz, Pierre E.; Kilcoyne, David A.L.; Monteiro, Paulo J.M.
• Is Part Of: Cement and concrete research. Volume 111(2018)
• Page Start: 130
• Page End: 137
• Publication Date: 2018-09
• Subjects: Tricalcium aluminate -- Hydration products -- Characterization -- X-ray diffraction -- Spectromicroscopy; Cement -- Periodicals; Cement -- Research -- Periodicals; Concrete -- Periodicals; Concrete -- Research -- Periodicals; Ciment -- Périodiques; Béton -- Périodiques; Cement; Concrete; Periodicals; 620.135
• DOI: 10.1016/j.cemconres.2018.06.002
• Languages: English
• ISSNs: 0008-8846

Abstract

Abstract: The rheology of modern Portland cement (PC) concrete critically depends on the correct dosage of gypsum (calcium sulfate hydrate) to control the hydration of the most reactive phase - tricalcium aluminate (C3 A). The underlying physio-chemical mechanism, however, remains unsolved mainly due to the lack of high-spatial-resolved and chemistry-sensitive characterization of the C3 A dissolution frontier. Here, we fill this gap by integrating synchrotron-radiation based crystallographic, photon-energy-dependent spectroscopic and high-resolution morphological studies of the C3 A hydration product layer. We propose that ettringite (6CaO·Al2 O3 ·SO3 ·32H2 O) is the only hydration product after the initial reaction period and before complete gypsum dissolution. We quantify the 2D and 3D morphology of the ettringite network, e.g. the packing density of ettringite at various surface locations and the surface dissolution heterogeneity. Our results show no trace of a rate-controlling diffusion barrier. We expect our work to have significant impact on modeling the kinetics and morphological evolution of PC hydration.