Search

This study investigates the relationships between the hydration kinetics of waterglass-activated slag and the development of its physical-mechanical properties, as well as its color change. To modify the calorimetric response of alkali-activated slag, hexylene glycol was selected from various alcohols for in-depth experiments. In presence of hexylene glycol, the formation of initial reaction products was restricted to the slag surface, which drastically slowed down the further consumption of dissolved species and slag dissolution and consequently delayed the bulk hydration of the waterglass-activated slag by several days. This allowed to show that the corresponding calorimetric peak is directly related to the rapid evolution of the microstructure and physical-mechanical parameters and to the onset of a blue/green color change recorded as a time-lapse video. Workability loss was correlated with the first half of the second calorimetric peak, while the most rapid increase in strengths and autogenous shrinkage was related to the third calorimetric peak. Ultrasonic pulse velocity increased considerably during both the second and third calorimetric peak. Despite the modified morphology of the initial reaction products, the prolonged induction period, and the slightly reduced degree of hydration induced by hexylene glycol, the overall mechanism of alkaline activation remained unchanged in the long-term perspective. It was hypothesized that the main issue of the use of organic admixtures in alkali-activated systems is the destabilizing effect of these admixtures on soluble silicates introduced into the system with an activator. [ABSTRACT FROM AUTHOR]

• Lignosulfonate efficient for NaOH activation regardless of the time of addition of paste components. • Calorimetry of alkali-activated slag with low silicate modulus of activator (0; 0.10; 0.25, 0.50). • Effect of lignosulfonate on rheology greatly related to its retarding effect on hydration. • The use and evaluation of strain amplitude sweep tests after different time discussed. • Hump on loss modulus curve for the pastes with significant precipitation of products. One of the crucial issues of alkali-activated materials is the application of conventional plasticizers. Lignosulfonate plasticizer (LS) works well for sodium hydroxide-activated slag but loses its efficiency in sodium waterglass-activated slag because of competitive adsorption with silicates. Therefore, the effects of the timing of LS and activator addition on the structural build-up and breakdown of AAS pastes with low-silicate moduli activator (0 to 0.50) were investigated, particularly by means of non-traditional strain sweep tests, which are thoroughly discussed. The rheological tests were correlated with the Vicat needle test and isothermal calorimetry. The results showed the high efficiency of LS in NaOH-activated slag paste over time, regardless of the order of addition of the components of the paste. It was accompanied by a considerable retardation effect of LS on the hydration of AAS. The beneficial effect of LS on the rheological parameters and hydration kinetics decreased rapidly with an increase of the silicate modulus of the activator. The delayed addition of the concentrated silicate-containing activators completely counteracted the slightly beneficial effect of LS and even accelerated the initial structural build-up. [ABSTRACT FROM AUTHOR]

The aim of this study was to explore the influence of ethylene glycol in a wide range of polymerization degree, i.e. from monomer (EG) up to polyethylene glycol (PEG) with molecular weight of about 35,000, on properties of alkali-activated slag mortars. Changes in molecular weight and dose of all tested glycols had only minor effect on compressive strength, while drying shrinkage was significantly affected by both these factors. EG had negligible impact on drying shrinkage, but other tested glycols reduced it significantly with PEG2000 and PEG10000 being the most effective. Such different shrinkage behavior was attributed to the changes in surface tension and pore structure. All tested glycols reduced the total heat released during the hydration and interestingly modified the heat flow depending on their molecular weight. [ABSTRACT FROM AUTHOR]

In recent years, the use of various nontraditional cements and composites has increased. Alkali-activated materials, especially those based on alkali activation of blast-furnace slag, have considerable potential in construction industry. However, alkali-activated slag binders exhibit significant shrinkage, in some circumstances several times greater than portland cement-based materials, which hinders wider use of these materials in numerous applications. Therefore, the use of specific admixtures suitable for alkaliactivated systems is necessary. This paper is consequently focused on testing the efficiency of shrinkage-reducing additives based on polypropylene glycols, as well as their influence on the hydration mechanism and mechanical properties of prepared alkali-activated materials. [ABSTRACT FROM AUTHOR]

Significant drying shrinkage is one of the main limitations for the wider utilization of alkali-activated slag (AAS). Few previous works revealed that it is possible to reduce AAS drying shrinkage by the use of shrinkage-reducing admixtures (SRAs). However, these studies were mainly focused on SRA based on polypropylene glycol, while as it is shown in this paper, the behavior of SRA based on 2-methyl-2,4-pentanediol can be significantly different. While 0.25% and 0.50% had only a minor effect on the AAS properties, 1.0% of this SRA reduced the drying shrinkage of waterglass-activated slag mortar by more than 80%, but it greatly reduced early strengths simultaneously. This feature was further studied by isothermal calorimetry, mercury intrusion porosimetry (MIP) and scanning electron microscopy (SEM). Calorimetric experiments showed that 1% of SRA modified the second peak of the pre-induction period and delayed the maximum of the main hydration peak by several days, which corresponds well with observed strength development as well as with the MIP and SEM results. These observations proved the certain incompatibility of SRA with the studied AAS system, because the drying shrinkage reduction was induced by the strong retardation of hydration, resulting in a coarsening of the pore structure rather than the proper function of the SRA. [ABSTRACT FROM AUTHOR]

Alkali-activated systems (AAS) represent an ecologically and economically sustainable inorganic binder as an alternative to ordinary Portland cement (OPC). One of the main benefits of AAS is their durability in aggressive environments, which can be equal or even better than that of OPC. In this paper, the influence of the type of alkaline activator in alkali-activated blast furnace slag (AAS) in terms of resistance to sulfur dioxide corrosion was investigated. The durability testing process was based on the CSN EN ISO 3231 standard and simultaneously compared with mortar samples prepared by using Blastfurnace cement CEM III/A 32.5R. The degradation progress was evaluated by employing several different methods such as observing the compressive strength development, weight change evaluation, non-destructive testing methods like ultrasound or impact echo technique, or visual phenolphthalein technique. Subsequently, fundamental characterization of samples by the XRD method was performed during the degradation test. The obtained results indicate that none of the testing methods used could be prioritized over others to determine the resistance of AAS against the action of sulfur dioxide. For this reason, the durability testing of AAS remains an issue, and the development of specific standards considering the behavior of AAS seems necessary. [ABSTRACT FROM AUTHOR]

The very early stages of alkaline activation of slag control its rheology and setting, but also affect its hydration, which occurs later. Simultaneously, these parameters are dictated by the nature and dose of the alkaline activator. Therefore, we investigated and compared the changes in slag particles (SEM, BET, laser diffraction), as well as in the pore solution composition (ICP–OES), pH, and conductivity, of alkali-activated slag (AAS) pastes containing the three most common sodium activators (waterglass, hydroxide, and carbonate) and water during the first 24 h of its activation. To ensure the best possible comparability of the pastes, a fairly nontraditional mixture design was adopted, based on the same concentration of Na+ (4 mol/dm3) and the same volume fraction of slag in the paste (0.50). The results were correlated with the pastes' hydration kinetics (isothermal calorimetry), structural build-up (oscillatory rheology), and setting times (Vicat). Great differences were observed in most of these properties, in the formation of hydration products, and in the composition of the pore solution for each activator. The results emphasize the role of the anionic groups in the activators and of the pH, which help predict the sample's behavior based on its calorimetric curve, and offer data for further comparisons and for the modelling of AAS hydration for specific activators. [ABSTRACT FROM AUTHOR]

There are many highly variable approaches to mix proportioning of alkali-activated materials (AAMs), which considerably contribute to their great complexity and often incomparability of the obtained results. Therefore, this paper suggests one specific approach, based on the molarity of the activator and the volume fraction of the precursor. First, an inherently simple calculation procedure is introduced to obtain the weights of the raw materials required to prepare a desired volume of AAM paste and possibly mortar or concrete. Second, the rationale for this approach is demonstrated using calorimetric experiments conducted on alkali-activated slag pastes, activated with sodium and potassium hydroxides, waterglasses, and carbonates in wide ranges of molarities. Third, the applicability and impact of the presented approach are discussed in-depth, considering practical applications. The overall outcome is a complex set of information emphasizing the importance of molarity, precursor volume fraction, and space-filling ability of the reaction products for different activators. • Mix designing of AAM based on activator molarity and precursor volume fraction • Space-filling ability of products for each activator also considered • Reaction kinetics of AAS mapped over the concentrations of six common activators • Molarity of 2 to 4 M Na+ or K+ recommended for slag activation • Impact of the presented approach and data discussed in a wide practical and scientific context [ABSTRACT FROM AUTHOR]