The effect of curing regime on the distribution ofAl3＋ coordination in hardened cement pastes within 28 d were investigated by 29Si and 27Al magic angle spinning （MAS） nuclear magnetic resonance（NMR） with deconvo...The effect of curing regime on the distribution ofAl3＋ coordination in hardened cement pastes within 28 d were investigated by 29Si and 27Al magic angle spinning （MAS） nuclear magnetic resonance（NMR） with deconvolution technique. The results indicate that the tetrahedral coordination Al3＋ incorporated in C-S-H structure mainly originate from the AP＋ incorporated in the alite and belite phases in the Portland cement. The curing regime of constant temperature of 20 ℃ is beneficial to the octahedral coordination Al3＋ transforming to tetrahedral coordination AP＋ incorporated in C-S-H structure. However, at curing regime of variable temperature, the temperature rising process is more advantageous to the transformation from ettringite to monosulphate, substitution of Al3＋ for Si4＋ in the C-S-H structure and the formation of the third aluminate hydrate （TAH） than that at constant temperature of 20 ℃. The high temperature of 60 ℃ in the holding temperature process promotes the decomposition of ettringite, and enhances the consumption of the Al3＋ incorporated in C-S-H phases and the Al3＋ in TAH for the monosulphate forming. The temperature decreasing promotes the transformation from monosulphate to ettringite, and increases the consumption of the Al3＋ incorporated in C-S-H phases, and then increases the quantity of the TAH.展开更多
基金Funded by the Major State Basic Research Development Program of China(973 Program)(No.2009CB623201)
文摘The effect of curing regime on the distribution ofAl3＋ coordination in hardened cement pastes within 28 d were investigated by 29Si and 27Al magic angle spinning （MAS） nuclear magnetic resonance（NMR） with deconvolution technique. The results indicate that the tetrahedral coordination Al3＋ incorporated in C-S-H structure mainly originate from the AP＋ incorporated in the alite and belite phases in the Portland cement. The curing regime of constant temperature of 20 ℃ is beneficial to the octahedral coordination Al3＋ transforming to tetrahedral coordination AP＋ incorporated in C-S-H structure. However, at curing regime of variable temperature, the temperature rising process is more advantageous to the transformation from ettringite to monosulphate, substitution of Al3＋ for Si4＋ in the C-S-H structure and the formation of the third aluminate hydrate （TAH） than that at constant temperature of 20 ℃. The high temperature of 60 ℃ in the holding temperature process promotes the decomposition of ettringite, and enhances the consumption of the Al3＋ incorporated in C-S-H phases and the Al3＋ in TAH for the monosulphate forming. The temperature decreasing promotes the transformation from monosulphate to ettringite, and increases the consumption of the Al3＋ incorporated in C-S-H phases, and then increases the quantity of the TAH.
