碳化作用
粉煤灰
熔渣(焊接)
材料科学
碱度
化学工程
硅酸铝
碱金属
碳化
冶金
化学
复合材料
有机化学
工程类
催化作用
作者
Susan A. Bernal,John L. Provis,Brant Walkley,Rackel San Nicolas,John D. Gehman,David G. Brice,Adam R. Kilcullen,Peter Duxson,J.S.J. van Deventer
标识
DOI:10.1016/j.cemconres.2013.06.007
摘要
Binders formed through alkali-activation of slags and fly ashes, including ‘fly ash geopolymers’, provide appealing properties as binders for low-emissions concrete production. However, the changes in pH and pore solution chemistry induced during accelerated carbonation testing provide unrealistically low predictions of in-service carbonation resistance. The aluminosilicate gel remaining in an alkali-activated slag system after accelerated carbonation is highly polymerised, consistent with a decalcification mechanism, while fly ash-based binders mainly carbonate through precipitation of alkali salts (bicarbonates at elevated CO2 concentrations, or carbonates under natural exposure) from the pore solution, with little change in the binder gel identifiable by nuclear magnetic resonance spectroscopy. In activated fly ash/slag blends, two distinct gels (C–A–S–H and N–A–S–H) are formed; under accelerated carbonation, the N–A–S–H gel behaves comparably to fly ash-based systems, while the C–A–S–H gel is decalcified similarly to alkali-activated slag. This provides new scope for durability optimisation, and for developing appropriate testing methodologies.
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