In situ soft X-ray spectromicroscopy of early tricalcium silicate hydration

Sungchul Bae, Manabu Kanematsu, Daniel Hernández-Cruz, Juhyuk Moon, David Kilcoyne, Paulo J.M. Monteiro

Research output: Contribution to journalArticle

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Abstract

The understanding and control of early hydration of tricalcium silicate (C3S) is of great importance to cement science and concrete technology. However, traditional characterization methods are incapable of providing morphological and spectroscopic information about in situ hydration at the nanoscale. Using soft X-ray spectromicroscopy, we report the changes in morphology and molecular structure of C3S at an early stage of hydration. In situ C3S hydration in a wet cell, beginning with induction (~1 h) and acceleration (~4 h) periods of up to ~8 h, was studied and compared with ex situ measurements in the deceleration period after 15 h of curing. Analysis of the near-edge X-ray absorption fine structure showed that the Ca binding energy and energy splitting of C3S changed rapidly in the early age of hydration and exhibited values similar to calcium silicate hydrate (C-S-H). The formation of C-S-H nanoseeds in the C3S solution and the development of a fibrillar C-S-H morphology on the C3S surface were visualized. Following this, silicate polymerization accompanied by C-S-H precipitation produced chemical shifts in the peaks of the main Si K edge and in multiple scattering. However, the silicate polymerization process did not significantly affect the Ca binding energy of C-S-H.

Original languageEnglish
Article number976
JournalMaterials
Volume9
Issue number12
DOIs
StatePublished - 2016 Jan 1

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Silicic Acid
Calcium silicate
Hydration
Silicates
Hydrates
X rays
Binding energy
Polymerization
Multiple scattering
Deceleration
X ray absorption
Chemical shift
Molecular structure
Curing
Cements
tricalcium silicate
Concretes
calcium silicate

Keywords

  • C-S-H
  • Hydration
  • Kinetics
  • Spectromicroscopy
  • Tricalcium silicate

Cite this

Bae, S., Kanematsu, M., Hernández-Cruz, D., Moon, J., Kilcoyne, D., & Monteiro, P. J. M. (2016). In situ soft X-ray spectromicroscopy of early tricalcium silicate hydration. Materials, 9(12), [976]. https://doi.org/10.3390/ma9120976
Bae, Sungchul ; Kanematsu, Manabu ; Hernández-Cruz, Daniel ; Moon, Juhyuk ; Kilcoyne, David ; Monteiro, Paulo J.M. / In situ soft X-ray spectromicroscopy of early tricalcium silicate hydration. In: Materials. 2016 ; Vol. 9, No. 12.
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Bae, S, Kanematsu, M, Hernández-Cruz, D, Moon, J, Kilcoyne, D & Monteiro, PJM 2016, 'In situ soft X-ray spectromicroscopy of early tricalcium silicate hydration', Materials, vol. 9, no. 12, 976. https://doi.org/10.3390/ma9120976

In situ soft X-ray spectromicroscopy of early tricalcium silicate hydration. / Bae, Sungchul; Kanematsu, Manabu; Hernández-Cruz, Daniel; Moon, Juhyuk; Kilcoyne, David; Monteiro, Paulo J.M.

In: Materials, Vol. 9, No. 12, 976, 01.01.2016.

Research output: Contribution to journalArticle

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AU - Bae, Sungchul

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AB - The understanding and control of early hydration of tricalcium silicate (C3S) is of great importance to cement science and concrete technology. However, traditional characterization methods are incapable of providing morphological and spectroscopic information about in situ hydration at the nanoscale. Using soft X-ray spectromicroscopy, we report the changes in morphology and molecular structure of C3S at an early stage of hydration. In situ C3S hydration in a wet cell, beginning with induction (~1 h) and acceleration (~4 h) periods of up to ~8 h, was studied and compared with ex situ measurements in the deceleration period after 15 h of curing. Analysis of the near-edge X-ray absorption fine structure showed that the Ca binding energy and energy splitting of C3S changed rapidly in the early age of hydration and exhibited values similar to calcium silicate hydrate (C-S-H). The formation of C-S-H nanoseeds in the C3S solution and the development of a fibrillar C-S-H morphology on the C3S surface were visualized. Following this, silicate polymerization accompanied by C-S-H precipitation produced chemical shifts in the peaks of the main Si K edge and in multiple scattering. However, the silicate polymerization process did not significantly affect the Ca binding energy of C-S-H.

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Bae S, Kanematsu M, Hernández-Cruz D, Moon J, Kilcoyne D, Monteiro PJM. In situ soft X-ray spectromicroscopy of early tricalcium silicate hydration. Materials. 2016 Jan 1;9(12). 976. https://doi.org/10.3390/ma9120976