Lucia Alarcon-Ruiz

Bio: Lucia Alarcon-Ruiz is an academic researcher. The author has contributed to research in topics: Thermal decomposition & Portlandite. The author has an hindex of 1, co-authored 1 publications receiving 559 citations.

Modification of phase evolution in alkali-activated blast furnace slag by the incorporation of fly ash

Abstract: The microstructural evolution of alkali-activated binders based on blast furnace slag, fly ash and their blends during the first six months of sealed curing is assessed. The nature of the main binding gels in these blends shows distinct characteristics with respect to binder composition. It is evident that the incorporation of fly ash as an additional source of alumina and silica, but not calcium, in activated slag binders affects the mechanism and rate of formation of the main binding gels. The rate of formation of the main binding gel phases depends strongly on fly ash content. Pastes based solely on silicate-activated slag show a structure dominated by a C–A–S–H type gel, while silicate-activated fly ash are dominated by N–A–S–H ‘geopolymer’ gel. Blended slag-fly ash binders can demonstrate the formation of co-existing C–A–S–H and geopolymer gels, which are clearly distinguishable at earlier age when the binder contains no more than 75 wt.% fly ash. The separation in chemistry between different regions of the gel becomes less distinct at longer age. With a slower overall reaction rate, a 1:1 slag:fly ash system shares more microstructural features with a slag-based binder than a fly ash-based binder, indicating the strong influence of calcium on the gel chemistry, particularly with regard to the bound water environments within the gel. However, in systems with similar or lower slag content, a hybrid type gel described as N–(C)–A–S–H is also identified, as part of the Ca released by slag dissolution is incorporated into the N–A–S–H type gel resulting from fly ash activation. Fly ash-based binders exhibit a slower reaction compared to activated-slag pastes, but extended times of curing promote the formation of more cross-linked binding products and a denser microstructure. This mechanism is slower for samples with lower slag content, emphasizing the correct selection of binder proportions in promoting a well-densified, durable solid microstructure.

Development of an eco-friendly Ultra-High Performance Concrete (UHPC) with efficient cement and mineral admixtures uses

Abstract: This paper addresses the development of an eco-friendly Ultra-High Performance Concrete (UHPC) with efficient cement and mineral admixtures uses are investigated. The modified Andreasen & Andersen particle packing model is utilized to achieve a densely compacted cementitious matrix. Fly ash (FA), ground granulated blast-furnace slag (GGBS) and limestone powder (LP) are used to replace cement, and their effects on the properties of the designed UHPC are analyzed. The results show that the influence of FA, GGBS or LP on the early hydration kinetics of the UHPC is very similar during the initial five days, while the hydration rate of the blends with GGBS is mostly accelerated afterwards. Moreover, the mechanical properties of the mixture with GGBS are superior, compared to that with FA or LP at both 28 and 91 days. Due to the very low water amount and relatively large superplasticizer dosage in UHPC, the pozzolanic reaction of FA is significantly retarded. Additionally, the calculations of the embedded CO2 emission demonstrate that the cement and mineral admixtures are efficiently used in the developed UHPC, which reduce its environmental impact compared to other UHPCs found in the literature.

Hydration and properties of nano-TiO2 blended cement composites

Abstract: Two types of nano-TiO2 particles were blended into cement pastes and mortars. Their effects on the hydration and properties of the hydrated cement pastes were investigated. The addition of nano-TiO2 powders significantly accelerated the hydration rate and promoted the hydration degree of the cementitious materials at early ages. It was demonstrated that TiO2 was inert and stable during the cement hydration process. The total porosity of the cement pastes decreased and the pore size distribution were also altered. The acceleration of hydration rate and the change of microstructure also affected the physical and mechanical properties of the cement-based materials. The initial and final setting time was shortened and more water was required to maintain a standard consistence due to the addition of the nano-TiO2. The compressive strength of the mortar was enhanced, practically at early ages. It is concluded that the nano-TiO2 acted as a catalyst in the cement hydration reactions.