TY - JOUR
T1 - Hydration of β-dicalcium silicate at high temperatures under hydrothermal conditions
AU - Yanagisawa, Kazumichi
AU - Hu, Xiulan
AU - Onda, Ayumu
AU - Kajiyoshi, Koji
PY - 2006/5
Y1 - 2006/5
N2 - Hydration of β-dicalcium silicate was carried out under hydrothermal conditions at different temperatures from 50 °C to 400 °C up to 5 days by using two methods to start the reactions at room temperature or at a desired reaction temperature. 9 C-S-H phases with the same Ca/Si ratio as precursor (γ-dicalcium silicate hydrate and α-dicalcium silicate hydrate and dellaite), Ca-rich compositions (jaffeite and reinhardbraunsite), Si-rich compositions (Ca8Si5O18, kilchoanite and foshagite), and C-S-H gel were obtained at the initial stage of the hydration of β-dicalcium silicate. The reaction products were different in dependence in the hydrothermal processes. It was found that α-dicalcium silicate hydrate was directly formed from β-dicalcium silicate at low temperatures below 220 °C. The products obtained at above 240 °C were different in dependence in the hydrothermal processes, due to the different decomposition route of γ-dicalcium silicate hydrate, the initial product from β-dicalcium silicate. The room temperature mixing method gave reinhardbraunsite and kilchoanite through Ca8Si5O18. In the case of the high temperature mixing method, γ-dicalcium silicate hydrate decomposed to from Ca8Si5O18 and reinhardbraunsite with jaffeite, then Ca8Si5O18 decomposed to from jaffeite and kilchoanite, and final products at 400 °C were reinhardbraunsite and foshagite which was formed from kilchoanite.
AB - Hydration of β-dicalcium silicate was carried out under hydrothermal conditions at different temperatures from 50 °C to 400 °C up to 5 days by using two methods to start the reactions at room temperature or at a desired reaction temperature. 9 C-S-H phases with the same Ca/Si ratio as precursor (γ-dicalcium silicate hydrate and α-dicalcium silicate hydrate and dellaite), Ca-rich compositions (jaffeite and reinhardbraunsite), Si-rich compositions (Ca8Si5O18, kilchoanite and foshagite), and C-S-H gel were obtained at the initial stage of the hydration of β-dicalcium silicate. The reaction products were different in dependence in the hydrothermal processes. It was found that α-dicalcium silicate hydrate was directly formed from β-dicalcium silicate at low temperatures below 220 °C. The products obtained at above 240 °C were different in dependence in the hydrothermal processes, due to the different decomposition route of γ-dicalcium silicate hydrate, the initial product from β-dicalcium silicate. The room temperature mixing method gave reinhardbraunsite and kilchoanite through Ca8Si5O18. In the case of the high temperature mixing method, γ-dicalcium silicate hydrate decomposed to from Ca8Si5O18 and reinhardbraunsite with jaffeite, then Ca8Si5O18 decomposed to from jaffeite and kilchoanite, and final products at 400 °C were reinhardbraunsite and foshagite which was formed from kilchoanite.
KW - Calcium-silicate-hydrates (C-S-H)
KW - High temperature mixing method
KW - Hydration
KW - Hydrothermal treatment
KW - β-Dicalcium silicate
UR - http://www.scopus.com/inward/record.url?scp=33646080810&partnerID=8YFLogxK
U2 - 10.1016/j.cemconres.2005.12.009
DO - 10.1016/j.cemconres.2005.12.009
M3 - 文章
AN - SCOPUS:33646080810
SN - 0008-8846
VL - 36
SP - 810
EP - 816
JO - Cement and Concrete Research
JF - Cement and Concrete Research
IS - 5
ER -