We have studied the influence of interaction between CaO-SiO2-H(2)Q JC-S-H)
gel and ettringite (AFt) on their dissolution regarding the initial chemic
al feature of degraded cement pore water. In this work, firstly dissolution
experiments were performed in C-S-H gel at Ca/Si=1.0, 1.2 and 1.47 coexist
ing with AFt of which amount was 5% of mol corresponding to each C-S-H gel.
Secondly, assuming the congruent dissolution of AFt, dissolution of the sa
me system was calculated by combining with the dissolution model of C-S-H g
el at 1<Ca/Si<less than or equal to>1.5, considering without interaction be
tween C-S-H gel and AFt. Measured and calculated results of Ca, Si, Al and
S total concentrations and pH values of C-S-H gel coexisting with AFt syste
m were investigated. Discrepancies between experimental and calculated Ca,
Si, Al and S total concentrations and pH values suggested the importance of
interaction phenomena in C-S-H gel coexisting with AFt system. By consider
ing the substitutions of Al(OH)(4)(-) and SO42- with Si tetrahedra in the s
tructure of C-S-H gel, these discrepancies are discussed in this study.