RESUMO
For geopolymers (usually composed of unreacted precursor and gel), the compressive strength is controlled by two factors. The first is the degree of reaction, or, equivalently, the amount of gel formed, including any calcium silicate hydrate gel in calcium-containing mixtures. The second factor is the gel composition, generally given by the Si/Al ratio. These two parameters are interrelated for typical silicate-activated metakaolin geopolymers. By separating out effects of Si/Al ratio and degree of reaction, this study quantitatively correlates the degree of reaction with the compressive strength of metakaolin-based geopolymers with and without calcium. Solid-state 29Si nuclear magnetic resonance (NMR) aided with chemical extractions was used to determine gel amounts and composition for several geopolymer mixtures. The compressive strength was also measured for each mixture at 7 days. Both the increase of Na/Al ratio in mixtures without calcium and addition of external calcium increased the degree of reaction, and compressive strength correlated linearly (R2 > 0.88) with the degree of reaction.
RESUMO
The microstructural development of mortar bars with silica glass aggregate undergoing alkali-silica reaction (ASR) under the conditions of American Society for Testing and Materials (ASTM) Standard Test C1260 was analyzed using scanning electron microscopy and qualitative X-ray microanalysis. Cracking in the aggregate, the hydrated paste, and the paste-aggregate interface was important in the development of the microstructure. Cracks were characterized according to their location, their relationship to other cracks, and whether they are filled with ASR gel. Expansion of the bars was approximately 1% at 12 days and 2% at 53 days. They fell apart by 63 days. The bars contained two zones, an inner region that was undergoing ASR and an outer and much more highly damaged zone that extended further inward over time. Evidence of ASR was present even during the period when specimens were immersed in water, prior to immersion in NaOH solution.
RESUMO
This work was undertaken to help understand and interpret the ultrasonic wave reflection response of Portland cement paste as it transforms from a fluid-like suspension to a solid in the first hours after mixing. A high impact polystyrene buffer (delay line) was used to measure small changes in the P- and S-wave reflection coefficients. Two materials were studied: a non-hydrating colloidal alumina suspension whose microstructure was manipulated between dispersed and flocculated states by adjusting the pH and a coarse silica suspension that readily sedimented. The S-wave reflection coefficient clearly distinguished between dispersed and flocculated states. Sedimentation of particles in dispersed suspensions was distinguished using the P-wave reflection coefficient. Based on these findings, the observed P- and S-wave responses from hydrating Portland cement paste are interpreted in terms of flocculation and sedimentation processes.
RESUMO
Ultrasonic wave reflection coefficients of aqueous solutions were measured using high-impact polystyrene as a buffer material to provide enhanced sensitivity over metal or ceramic buffer materials. The wave reflection values showed linear reduction when the concentration of chemical species in solution was increased, but a distinct relation between concentration and reflection coefficient was obtained for each solute species tested. However, more unified relationships were observed between reflection coefficient and other solution parameters - solution density, acoustic impedance, and P-wave velocity - that were consistent for all solution species. Based on this behavior an expression to compute solution density solely from reflection coefficient is derived, which can be applied to estimate solution density in solutions of unknown solute species and concentration when other measurements, such as wave velocity, are not possible.