Composition, silicate anion structure and morphology of calcium silicate hydrates (C-S-H) synthesised by silica-lime reaction and by controlled hydration of tricalcium silicate (C3S)

被引:101
|
作者
Rodriguez, E. Tajuelo [1 ]
Richardson, I. G. [1 ]
Black, L. [1 ]
Boehm-Courjault, E. [2 ]
Nonat, A. [3 ]
Skibsted, J. [4 ,5 ]
机构
[1] Univ Leeds, Sch Civil Engn, Leeds LS2 9JT, W Yorkshire, England
[2] Ecole Polytech Fed Lausanne, Lab Construct Mat, Lausanne, Switzerland
[3] Univ Bourgogne, CNRS, UMR 6303, Carnot Interdisciplinary Lab, Dijon, France
[4] Aarhus Univ, Dept Chem, DK-8000 Aarhus, Denmark
[5] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, Aarhus, Denmark
关键词
C-S-H; C3S hydration; Morphology; TEM-EDX; Portland cement; Si-29 MAS NMR; PORTLAND-CEMENT; DICALCIUM SILICATE; ROOM-TEMPERATURE; CELL DIMENSIONS; SOLID-SOLUTIONS; X-RAY; NMR; MICROSTRUCTURE; MICROANALYSIS; PASTES;
D O I
10.1179/1743676115Y.0000000038
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The main product of Portland cement hydration is C-S-H. Despite constituting more than half of the volume of hydrated pastes and having an important role in strength development, very little is known about the factors that determine its morphology. To investigate the relationship between the chemical composition, silicate anion structure and morphology of C-S-H, samples were synthesised via silica-lime reactions and by the hydration of C3S under controlled lime concentrations and with/without accelerators. The silicate anion structure of the samples was studied by Si-29 magic angle spinning nuclear magnetic resonance spectroscopy and the morphology and chemical composition by TEM and SEM. All samples prepared via silica-lime reactions with bulk Ca/Si up to 1.5 were foil-like. The hydration of C3S at fixed lime concentration yielded foil-like C-S-H for [CaO] < 22 mmol L-1 and fibrillar C-S-H for [CaO] > 22 mmol L-1. A relationship between the silicate anion structure and the morphology of C-S-H was found for the samples fabricated with accelerators.
引用
收藏
页码:362 / 371
页数:10
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