Si-29 magic-angle spinning nuclear magnetic resonance (MASNMR) nas used to
study the room-temperature hydration of C3S, beta-C2S, and reactive beta-C2
S mixed with different amounts of silica fume (SF) that had been hydrated u
p to nine months and longer, The overall CaO:SiO2 molar ratios of the mixes
were 0.12, 0.20, 0.35, 0.50, and 0.80, NMR spectroscopy was used to quanti
fy the remaining starting materials and the resulting hydration products of
different species. A broad peak assigned to Q(3), appearing in both the fo
urier transform (FT) and the cross-polarization (CP) modes, increased in in
tensity with increased SF content and with age. This Q(3) species was attri
buted to two sources: (1) the surface hydroxylation of SF and (2) the cross
-linking of dreierketten (chains of silicate tetrahedra arranged in a repea
ting three-unit conformation) in the calcium silicate hydrate (C-S-H) struc
ture. A Q(4) species also appeared in the CP spectra of samples with large
SF additions after extended hydration and was attributed to cross-polarizat
ion by adjacent hydroxylated Q(3) species at the surface of amorphous SiO2.