Intrinsic differences in atomic ordering of calcium (alumino)silicate hydrates in conventional and alkali-activated cements

被引:68
作者
White, Claire E. [1 ,2 ,3 ,4 ]
Daemen, Luke L. [3 ]
Hartl, Monika [3 ]
Page, Katharine [3 ]
机构
[1] Princeton Univ, Dept Civil & Environm Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Andlinger Ctr Energy & Environm, Princeton, NJ 08544 USA
[3] Los Alamos Natl Lab, Manuel Lujan Jr Neutron Scattering Ctr, Los Alamos, NM 87545 USA
[4] Los Alamos Natl Lab, Los Alamos, NM USA
关键词
X-ray diffraction (B); Calcium-silicate-hydrate (C-S-H) (B); Amorphous material (B); Alkali-activated cement; Portland cement (D); C-S-H; SODIUM ALUMINOSILICATE; CRYSTAL-STRUCTURE; SILICATE-HYDRATE; LOCAL-STRUCTURE; SLAG; METAKAOLIN; GEOPOLYMER; EVOLUTION; KINETICS;
D O I
10.1016/j.cemconres.2014.08.006
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The atomic structures of calcium silicate hydrate (C-S-H) and calcium (-sodium) aluminosilicate hydrate (C-(N)-A-S-H) gels, and their presence in conventional and blended cement systems, have been the topic of significant debate over recent decades. Previous investigations have revealed that synthetic C-S-H gel is nanocrystalline and due to the chemical similarities between ordinary Portland cement (OPC)-based systems and low-CO2 alkali-activated slags, researchers have inferred that the atomic ordering in alkali-activated slag is the same as in OPC-slag cements. Here, X-ray total scattering is used to determine the local bonding environment and nanostructure of C(-A)-S-H gels present in hydrated tricalcium silicate (C3S), blended C3S-slag and alkali-activated slag, revealing the large intrinsic differences in the extent of nanoscale ordering between C-S-H derived from C3S and alkali-activated slag systems, which may have a significant influence on thermodynamic stability, and material properties at higher length scales, including long term durability of alkali-activated cements. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:66 / 73
页数:8
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