共 46 条
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
相关论文