The role of composition in the structure and water-binding in alkali-silica reaction sol and gel

被引:7
|
作者
Rashidi, Mehdi [1 ]
Paul, Alvaro [2 ]
Do, Changwoo [3 ]
Kurtis, Kimberly E. [1 ]
机构
[1] Georgia Inst Technol, Sch Civil & Environm Engn, 790 Atlantic Dr, Atlanta, GA 30332 USA
[2] Univ Los Andes, Fac Ingn & Ciencias Aplicadas, Monsenor Alvaro Portillo 12455, Santiago, Chile
[3] Oak Ridge Natl Lab, Neutron Scattering Div, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
Characterization (B); Amorphous material (B); Alkali-aggregate reaction (C); Rheology (A); Small-angle neutron scattering; NUCLEAR-MAGNETIC-RESONANCE; SMALL-ANGLE SCATTERING; C-S-H; ASR GEL; NMR; AGGREGATION; ELECTROLYTE; VISCOSITY; CATIONS; SODIUM;
D O I
10.1016/j.cemconres.2019.105814
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The discrepancy between alkali cation (Na+) used in accelerated assessments of potential alkali-silica reactivity (ASR) and those predominant in portland cements (larger amounts of K+ than Na+) leads to questions regarding the reliability of standardized test methods to predict concrete field performance. To better understand the role of alkali cation type in ASR, this study investigates the influence of alkali cation type on the structure and water-binding ability of ASR sols and gels of varying composition. Results obtained by small-angle neutron scattering, H-1 NMR relaxometry, and rheological measurements indicate the formation of densified agglomerate structures with increasing silica-to-alkali molar mass ratios (S/A). However, Na-based sols exhibit a greater tendency to agglomerate and a higher dynamic viscosity than K-based ones. Furthermore, at high S/A, H-1 NMR relaxometry shows the greater ability of K-based gels to bind water, suggesting the better dispersion of siliceous structures and the development of finer porosities.
引用
收藏
页数:12
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