Please use this identifier to cite or link to this item: https://doi.org/10.3390/ma10020131
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dc.titleEffects of incorporating high-volume fly ash into tricalcium silicate on the degree of silicate polymerization and aluminum substitution for silicon in calcium silicate hydrate
dc.contributor.authorBae, S
dc.contributor.authorTaylor, R
dc.contributor.authorKilcoyne, D
dc.contributor.authorMoon, J
dc.contributor.authorMonteiro, P.J.M
dc.date.accessioned2020-10-26T03:01:44Z
dc.date.available2020-10-26T03:01:44Z
dc.date.issued2017
dc.identifier.citationBae, S, Taylor, R, Kilcoyne, D, Moon, J, Monteiro, P.J.M (2017). Effects of incorporating high-volume fly ash into tricalcium silicate on the degree of silicate polymerization and aluminum substitution for silicon in calcium silicate hydrate. Materials 10 (2) : 131. ScholarBank@NUS Repository. https://doi.org/10.3390/ma10020131
dc.identifier.issn1996-1944
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179768
dc.description.abstractThis study assesses the quantitative effects of incorporating high-volume fly ash (HVFA) into tricalcium silicate (C 3 S) paste on the hydration, degree of silicate polymerization, and Al substitution for Si in calcium silicate hydrate (C-S-H). Thermogravimetric analysis and isothermal conduction calorimetry showed that, although the induction period of C 3 S hydration was significantly extended, the degree of hydration of C 3 S after the deceleration period increased due to HVFA incorporation. Synchrotron-sourced soft X-ray spectromicroscopy further showed that most of the C 3 S in the C 3 S-HVFA paste was fully hydrated after 28 days of hydration, while that in the pure C 3 S paste was not. The chemical shifts of the Si K edge peaks in the near-edge X-ray fine structure of C-S-H in the C 3 S-HVFA paste directly indicate that Al substitutes for Si in C-S-H and that the additional silicate provided by the HVFA induces an enhanced degree of silicate polymerization. This new spectromicroscopic approach, supplemented with 27 Al and 29 Si magic-angle spinning nuclear magnetic resonance spectroscopy and transmission electron microscopy, turned out to be a powerful characterization tool for studying a local atomic binding structure of C-S-H in C 3 S-HVFA system and presented results consistent with previous literature. © 2017 by the authors.
dc.publisherMDPI AG
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectAluminum
dc.subjectCalcium
dc.subjectConcrete beams and girders
dc.subjectCrystal atomic structure
dc.subjectFly ash
dc.subjectHigh resolution transmission electron microscopy
dc.subjectHydrates
dc.subjectHydration
dc.subjectMagic angle spinning
dc.subjectMagnetic resonance spectroscopy
dc.subjectNuclear magnetic resonance spectroscopy
dc.subjectPolymerization
dc.subjectSilicate minerals
dc.subjectSilicates
dc.subjectSilicon
dc.subjectThermogravimetric analysis
dc.subjectTransmission electron microscopy
dc.subjectCalcium silicate hydrate
dc.subjectHydration products
dc.subjectIsothermal conduction calorimetries
dc.subjectMagic angle spinning nuclear magnetic resonance spectroscopy
dc.subjectSilicate polymerizations
dc.subjectSoft x-ray spectromicroscopy
dc.subjectTricalcium silicate
dc.subjectX ray microscopy
dc.subjectCalcium silicate
dc.typeArticle
dc.contributor.departmentCIVIL AND ENVIRONMENTAL ENGINEERING
dc.description.doi10.3390/ma10020131
dc.description.sourcetitleMaterials
dc.description.volume10
dc.description.issue2
dc.description.page131
dc.published.statepublished
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