quasi-elastic neutron scattering study on the water dynamics and reaction mechanisms in alkali-activated slags
In this study, in situ quasi-elastic neutron scattering (QENS) has been employed to probe the water dynamics and reaction mechanisms occurring during the formation of NaOH- and Na 2 SiO 3 -activated slags, an important class of low-CO 2 cements, in conjunction with isothermal conduction calorimetry...
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Published in | Physical chemistry chemical physics : PCCP Vol. 21; no. 2; pp. 1277 - 1292 |
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Main Authors | , , , |
Format | Journal Article |
Published |
22.05.2019
|
Online Access | Get full text |
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Summary: | In this study,
in situ
quasi-elastic neutron scattering (QENS) has been employed to probe the water dynamics and reaction mechanisms occurring during the formation of NaOH- and Na
2
SiO
3
-activated slags, an important class of low-CO
2
cements, in conjunction with isothermal conduction calorimetry (ICC), Fourier transform infrared spectroscopy (FTIR) analysis and N
2
sorption measurements. We show that the single ICC reaction peak in the NaOH-activated slag is accompanied with a transformation of free water to bound water (from QENS analysis), which directly signals formation of a sodium-containing aluminum-substituted calcium-silicate-hydrate (C-(N)-A-S-H) gel, as confirmed by FTIR. In contrast, the Na
2
SiO
3
-activated slag sample exhibits two distinct reaction peaks in the ICC data, where the first reaction peak is associated with conversion of constrained water to bound and free water, and the second peak is accompanied by conversion of free water to bound and constrained water (from QENS analysis). The second conversion is attributed to formation of the main reaction product (
i.e.
, C-(N)-A-S-H gel) as confirmed by FTIR and N
2
sorption data. Analysis of the QENS, FTIR and N
2
sorption data together with thermodynamic information from the literature explicitly shows that the first reaction peak is associated with the formation of an initial gel (similar to C-(N)-A-S-H gel) that is governed by the Na
+
ions and silicate species in Na
2
SiO
3
solution and the dissolved Ca/Al species from slag. Hence, this study exemplifies the power of
in situ
QENS, when combined with laboratory-based characterization techniques, in elucidating the water dynamics and associated chemical mechanisms occurring in complex materials, and has provided important mechanistic insight on the early-age reactions occurring during formation of two alkali-activated slags.
Determination of key amorphous-amorphous phase transformations in alkali-activated slags by combining
in situ
quasi-elastic neutron scattering and isothermal calorimetry. |
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Bibliography: | 2 3 Electronic supplementary information (ESI) available: Fits of the quasi-elastic neutron scattering data with a single-Lorentzian model; inelastic neutron scattering data: water librational peak; estimation of the average number of H cumulative heat for NaOH-activated slag - initial 2.5 hours; analysis of the FTIR data for NaOH-activated slag; surface area and hydrotalcite formation during the initial hour of reaction in the NaOH-activated slag and their potential impacts on BWI; determination of the enthalpy of generating bound H-atoms; BJH pore size distribution from N 10.1039/c9cp00889f O molecules solvating each ion in alkaline solutions; isothermal conduction calorimetry (ICC) data for a metakaolin-water mixture; BWI/CWI/FWI activated slag. See DOI SiO versus sorption; evolution of CWI and FWI as a function of time for the Na |
ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/c9cp00889f |