Impact of water content on the performance of alkali-activated slag concretes

In this study, we report the effect of varying the water/binder (w/b) ratio on the performance of sodium silicate activated concretes. Compressive strength development and water transport properties of these concretes were assessed, along with their resistance to carbonation. The results demonstrate that varying the water content within a reasonable range induced negligible changes in the compressive strengths of these concretes, when a constant paste content was used. A direct correlation between the w/b ratio and the amount of permeable voids in the concretes was not identified. The carbonation behaviour of these concretes changes prominently depending on the CO2 concentration of exposure, meaning that comparable accelerated carbonation rates were observed at varying w/b ratios, conversely to observations under natural carbonation conditions where w/b was significant in defining the carbonation rate

The Effect of Aggregate Particle Size on Formation of Geopolymeric Gel

Due to enhanced mechanical and chemical properties, geopolymeric materials are a potential alternative to ordinary Portland cement and high-strength cement for the construction industry. The effects of aggregate particle size on the formation and the mechanical properties of geopolymeric materials are investigated in the current work. The addition of soluble silicates to the alkaline activator was found to increase the dissolution of silicate ions from the aggregate into the geopolymer binder phase. The results indicate that the surface area of aggregate influences the strength development of a geopolymer

Phase evolution of C-(N)-A-S-H/N-A-S-H gel blends investigated via alkali-activation of synthetic calcium aluminosilicate precursors

Stoichiometrically-controlled alkali-activated pastes containing calcium-(sodium) aluminosilicate hydrate (C-(N)-A-S-H) and sodium aluminosilicate hydrate (N-A-S-H) gels are produced by alkali-activation of high-purity synthetic calcium aluminosilicate powders. These powders are chemically comparable to the glass in granulated blast furnace slag, but without interference from minor constituents. The physiochemical characteristics of these gels depend on precursor chemical composition. Increased Ca content of the precursor promotes formation of low-Al, high-Ca C-(N)-A-S-H with lower mean chain length as determined by quantification of solid state nuclear magnetic resonance spectra, and less formation of calcium carboaluminate ‘Alumino-ferrite mono’ (AFm) phases. Increased Al content promotes Al inclusion and reduced crosslinking within C-(N)-A-S-H, increased formation of calcium carboaluminate AFm phases, and formation of an additional N-A-S-H gel. Small changes in precursor composition can induce significant changes in phase evolution, nanostructure and physical properties, providing a novel route to understand microstructural development in alkali-activated binders and address key related durability issues

Synthesis of stoichiometrically controlled reactive aluminosilicate and calcium-aluminosilicate powders

Aluminosilicate and calcium-aluminosilicate powders are synthesised via an organic steric entrapment route under conditions permitting strict stoichiometric control, utilising polyvinyl alcohol and polyethylene glycol as polymeric carriers. Polyethylene glycol is superior to polyvinyl alcohol for synthesis of calcium-aluminosilicate powders via this method, producing a more controllable product which generated less fine ash during calcination. This paper presents detailed description of synthesis and characterisation of the powders produced through this approach, including new insight into the nanostructures within the calcined powders. Aluminium environments are a mixture of 4-, 5- and 6-coordinated, while silicon is tetrahedral and shows a broad range of connectivity states. The powders are X-ray amorphous, display a high degree of homogeneity, and thus offer potential for utilisation as precursors for synthesis of hydrous aluminosilicates in the quaternary CaO-Na2O-Al2O3-SiO2 system

MgO content of slag controls phase evolution and structural changes induced by accelerated carbonation in alkali-activated binders

The structural development and carbonation resistance of three silicate-activated slags (AAS) with varying MgO contents ( 5%), hydrotalcite is identified as the main secondary product in addition to C–A–S–H. Higher extent of reaction and reduced Al incorporation in the C–S–H product are observed with higher MgO content in the slag. These gel chemistry effects, and particularly the formation of hydrotalcite, seem to reduce the susceptibility to carbonation of AAS produced with higher MgO contents, as hydrotalcite appears to act as an internal CO2 sorbent. This is evidenced by an inverse relationship between natural carbonation depth and slag MgO content, for paste samples formulated at constant water/binder ratio. Thus, the carbonation performance of AAS can be enhanced by controlling the chemistry of the precursors

Gel nanostructure in alkali-activated binders based on slag and fly ash, and effects of accelerated carbonation

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