Decalcification shrinkage of cement paste

被引:312
作者
Chen, Jeffrey J.
Thomas, Jeffrey J. [1 ]
Jennings, Hamlin A.
机构
[1] Northwestern Univ, Dept Civil & Environm Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
calcium silicate hydrate (C-S-H); shrinkage; degradation; carbonation;
D O I
10.1016/j.cemconres.2005.11.003
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Decalcification of cement paste in concrete is associated with several modes of chemical degradation including leaching, carbonation and sulfate attack. The primary aim of the current study was to investigate the effects of decalcification under saturated conditions on the dimensional stability of cement paste. Thin (0.8 mm) specimens of tricalcium silicate (C3S) paste, white portland cement (WPC) paste, and WPC paste blended with 30% silica fume (WPC/30% SF) were decalcified by leaching in concentrated solutions of ammonium nitrate, a method that efficiently removes calcium from the solid while largely preserving silicate and other ions. All pastes were found to shrink significantly and irreversibly as a result of decalcification, particularly when the Ca/Si ratio of the C-S-H gel was reduced below similar to 1.2. Since this composition coincides with the onset of structural changes in C-S-H such as an increase in silicate polymerization and a local densification into sheet-like morphologies, it is proposed that the observed shrinkage, here called decalcification shrinkage, is due initially to these structural changes in C-S-H at Ca/Si similar to 1.2 and eventually to the decomposition of C-S-H into silica gel. In agreement,with this reasoning, the blended cement paste exhibited greater decalcification shrinkage than the pure cement pastes due to its lower initial Ca/Si ratio for C-S-H gel. The similarities in the mechanisms of decalcification shrinkage and carbonation shrinkage are also discussed. (C) 2005 Published by Elsevier Ltd.
引用
收藏
页码:801 / 809
页数:9
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