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Partial replacement and co-hydration of calcium aluminate cement (CAC) with ladle slag was investigated in this study as a pathway in valorizing the slag and reducing the economic cost of CAC. The impact of this replacement on the physical and microstructural properties were analysed using different techniques such as mechanical strength test, freeze-thaw, sulfate attack, XRD, SEM etc. Thermodynamic modelling was used to predict the phase assemblages of the blended cement using the hydration kinetics of the system. Experimental results showed the reference CAC mortar and the substituted mortar exhibited comparable strength gain at 7 and 28 days, and durability as measured by sulfate attack, abrasion, and freeze-thaw resistance. A low water-to-binder ratio (0.35) lessened the effect of conversion on the hydrates, as XRD showed metastable CAH₁₀ and C₂AH7.5 as the hydrates at 7, 28 and 60 days. This however can convert later to the thermodynamically stable phase C₃AH₆. Thermodynamic modelling suggests these two metastable phases as major binding phases, while Si-hydrogarnet and FeOOH appeared a minor trace in the binder. *Cement chemistry notation used, where C = CaO, A = Al₂O₃ and H = H₂O

In this work, we compared the main characteristics of highly porous geopolymer components for water treatment applications manufactured by 3D printing, direct foaming, or granulation. Furthermore, different approaches to impregnate the materials with Ag or Cu were evaluated to obtain filters with disinfecting or catalytic properties. The results revealed that all of the investigated manufacturing methods enabled the fabrication of components that possessed mesoporosity, suitable mechanical strength, and water permeability, even though their morphologies were completely different. Total porosity and compressive strength values were 28 vol% and 16 MPa for 3D-printed, 70–79 vol% and 1 MPa for direct-foamed, and 27 vol% and 10 MPa for granule samples. Both the filter preparation and the metal impregnation method affected the amount, oxidation state, and stability of Ag and Cu in the filters. However, it was possible to prepare filters with low metal leaching between a pH of 3–7, so that the released Ag and Cu concentrations were within drinking water standards.

The upgradation of the ilmenite ore, using a pyrometallurgy method, is performed using a carbothermic reduction of the ilmenite. A high titania slag is obtained which is used as a feedstock for the TiO2 pigment production. The slag is cooled after tapping in big molds and can take ten days to cool. This cooling method has remained the same since the inception of ilmenite smelting and recently rapid cooling through granulation has been utilized. The work presented in this paper focuses on the microstructural study of the slags that were prepared using different techniques and cooled at different cooling rates. Various analytical techniques, such as X-ray powder diffraction (XRD), scanning electron microscopy (SEM), inductively coupled plasma-optical emission spectroscopy (ICP-OES), and X-ray photoelectron spectroscopy (XPS) were used to exhibit the similarity of these synthetic slags to the properties of high titania ilmenite slag. The slag consisted mostly of pseudo-brookite phase with a M3O5 stoichiometry and smaller amounts of silicate and rutile phase. A glassy phase of silica was observed and most of the impurities were found to be present in the silicate phase. These silica phases were observed to be separate from the pseudo-brookite phase and along the phase boundaries. Micro-cracking of the slag surface, which is the characteristic of the M3O5 phase formed in the ilmenite slag, were observed under the SEM analysis. The XPS analysis revealed that faster cooling does result in lower amount of oxidation but the difference in the TiO2 and Ti2O3 composition can have larger impact on oxidation than the cooling speed.

Sol-gel processing allows synthesis of low-energy glasses. In this work, binary magnesium silicate glasses with various MgO contents are synthesized using a modified sol-gel route. TGA and XRD analyses indicate that amorphous glasses with up to 50 mol% MgO can be obtained at 500°C. The reactivity of the glasses is evaluated to assess the use of the sol-gel technique in the large-scale synthesis of alternative cementitious materials. Reactivity tests show that, as MgO content increases, reactivity of glasses increases, reaches an optimum and then declines. This trend doesn’t agree with the theoretical one estimated by NBO/T value, which is generally used for the evaluation of glass reactivity. Mg²⁺ ions play a role as the network modifier when first introduced to silicate glasses. This leads to the depolymerization of the networks, causing an increase in reactivity. Then the magnesium partly behaves as a network former, bonding with oxygens to form MgOₓ polyhedron when there are insufficient primary glass-forming oxide SiO₂, resulting in the polymerization of networks, hence the decrease in reactivity.

This paper reports on the synthesis and characteristics of a novel aluminosilicate glass-based cementitious binder. We investigated the hydration kinetics, degree of reaction, and phase assemblage of the glass via XRD, DTG, ²⁷Al and ²⁹Si MAS NMR, FTIR, SEM/EDS and thermodynamic modelling. The glass exhibits hydraulic properties in which the binder developed impressive compressive strength at early age. The main hydration products are an intermixed of Na and/or Al incorporated in C–S–H gel. Hydrotalcite precipitated with slower rate and thus may generate crystallization pressure on the binder at late stage. The glass reached a high degree of hydration (ca. 73 % based on quantitative ²⁹Si NMR analysis) without using any activators or co-binding systems. Therefore, the developed glass reported herein has high potential as a new low-carbon cementitious binder since it can be synthesised from naturally occurring carbonate free silicate minerals.

One-part alkali-activated materials prepared with solid-form alkali activator are gaining attention in the construction industry, as they are an easier and safer approach for cast-in-situ applications in comparison with two-part approach (i.e., involving the use of alkali-activator solutions). The present study compares the one-part and conventional two-part mixing methods with two aluminosilicate precursors, metakaolin and ground granulated blast-furnace slag, using identical mix designs (in terms of molar ratios of SiO2, Al2O3, and Na2O) with both preparation methods. The results revealed that using one-part mix delays the setting time, increases the heat of reaction, decreases the shrinkage, and reaches between 80 and 85% of the compressive strength of the two-part mix. In addition, scanning electron microscopy, thermogravimetric analysis, and X-ray diffraction analysis showed no major differences between one- and two-part. However, energy-dispersive X-ray spectroscopy and magic angle spinning nuclear magnetic resonance experiments indicated that the extent of reaction in two-part alkali-activated mixes is higher than for one-part. Graphical Abstract

Ways to reduce cement-related carbon emissions are actively sought. One possible solution is partial substitution of Portland cement by alkali-reactive glass. We report on low-CO2 glass compositions that have high alkali solubility derived from industrial basaltic stone wool compositions. We found that highly alkali-soluble glasses can be formed with glass compositions that in principle can be made using silicate minerals which have no raw material-related CO2 emissions. The reason behind the reactivity of these glasses is thought to be caused by the dilution of the main network-forming species, silicon, which is further enhanced by phase separation, forming phases with high-silicon and low-silicon concentrations. Phase separation in alumina-rich samples is further studied and occurs at moderate cooling rates. The effect of glass-glass phase separation is discussed in the context of reactive glasses in cementitious systems. The results indicate that controlled phase separation could decouple CO2 emissions from the reactivity of glassy supplementary cementitious materials.

There is some ambiguity regarding the fate of Mg during the alkali activation of Mg-rich precursors within the broader field of alkali activated materials (AAMs). The present work addresses this issue by studying the reaction products in AAMs synthesized from (Na-Mg) aluminosilicate glasses. Here, instead of magnesium silicate hydrate (M-S-H) phase, Mg exclusively forms an amorphous magnesium silicate (AMS) phase. Compared to M-S-H, AMS is a more depolymerized phase, which has not previously been well documented. The formation of AMS seems to be driven by the high charge density of the Mg cation which effectively stabilizes the depolymerized silicate species. We also show that the lack of hydrotalcite-group phases is due to aluminum depletion by zeolite formation. This work highlights the need to consider the existence of the AMS phase in Mg-containing AAMs, especially in complex systems, where its identification may be difficult.

This paper focuses on the development of high-strength and eco-friendly one-part (i.e., dry-mix) alkali-activated mortar with ground granulated blast furnace slag as the main precursor. In addition to slag, phyllite dust and silica fume were used as co-binders in binary and ternary blends to improve mechanical properties. Particle packing optimization was employed for the mix proportioning to achieve a compact matrix skeleton. The results revealed that a 10% increase in mortar strength was gained after adjusting the particle packing and an additional 20% increment was observed after blending the slag with other mineral admixtures. Ternary blend with all three binders achieved a mortar compressive strength value of 145 MPa (at 28 d age), which is the highest strength reported in one-part alkali-activated materials. Additionally, ternary blends present potential economic benefits because of their ability to replace slag with lower-cost industrial side streams.

Alkali-activated materials (AAMs), sometimes called geopolymers, are eco-friendly cementitious materials with reduced carbon emissions when compared to ordinary Portland cement. However, the availability of most precursors used for AAM production may decline in the future because of changes in industrial sectors. Thus, new precursors must be developed. Recently there has been increased interest in synthetic glass precursors. One major concern with using synthetic glasses is ensuring that they react sufficiently under alkaline conditions. Reactivity is a necessary, although not sufficient, requirement for a suitable precursor for AAMs. This work involves the synthesis, characterization, and estimation of alkaline reactivity of Na-Mg aluminosilicate glasses. Structural characterization showed that replacing Na with Mg led to more depolymerization. Alkaline reactivity studies indicated that, as Mg replaced Na, reactivity of glasses increased at first, reached an optimal value, and then declined. This trend in reactivity could not be explained by the conventional parameters used for estimating glass reactivity: the non-bridging oxygen fraction (which predicts similar reactivity for all glasses) and optical basicity (which predicts a decrease in reactivity with an increase in Mg replacement). The reactivity of the studied glasses was found to depend on two main factors: depolymerization (as indicated by structural characterization) and optical basicity. Depolymerization dominated initially, which led to an increase in reactivity, while the effect of optical basicity dominated later, leading to a decrease in reactivity. Hence, while designing reactive synthetic glasses for alkali activation, structural study of glasses should be given due consideration in addition to the conventional factors.

Aluminosilicate glasses are materials with a wide range of technological applications. The field strength of network-modifying cations strongly influences the structure of aluminosilicate glasses and their suitability for various applications. In this work, we study the influence of the field strength of network-modifying cations on the structure of [(Na₂O)1–x(MgO)ₓ(Al₂O₃)0·25(SiO₂)1·25] glasses. Due to the higher cation field strength of magnesium than sodium, magnesium prefers the role of network modifier, while sodium preferentially acts as a charge compensator. When magnesium replaces sodium as network modifier, Q³ silicon species are converted into Q² species. The replacement of sodium with magnesium as charge compensator leads to the following changes: (1) the proportion of aluminum-rich Q⁴ species [Q⁴(4Al) and Q⁴(3Al)] decreases, while the proportion of aluminum-deficient Q⁴ species [Q⁴(2Al) and Q⁴(1Al)] increases; and (2) there is an increased tendency for phase separation between silica-rich and alumina-rich glasses.

The role of organic ligands on the formation of hydrated magnesium carbonates (HMCs) has been remaining unclear. This work reports insights into the effects of Mg-acetate on the carbonation of brucite including the kinetics of reaction, the precipitation of different HMCs, and reaction mechanisms. We found that the organic ligand increases the kinetics of brucite's carbonation and alter the formation and conversion of HMCs. A relatively unknown phase (i.e., giorgiosite) precipitates in the presence of Mg-acetate with nanowire morphology. With the presence of acetate ligand, nucleation sites formed after the breakdown of Mg-acetate complexes and be replaced by the Mg–CO3 bonds. These sites act as a sink for Mg2+ to grow crystals and prevent the passivation layer of HMCs on brucite's surface. Findings reported here can enable an approach to steer pore solution chemistry in the HMC-based binder for better reaction degree, durability, and mechanical properties.

Ladle slag, a by-product of steelmaking process, has shown potential to be used as a cementitious material in construction. However, the stability of the hydration products has not been investigated, and has been found to depend on available water. This paper presents the investigation of ladle slag hydration at different water-to-binder ratios. Hydrates of ladle slag converts from metastable to a stable reaction product over a period of time, thus affecting the mechanical and microstructural properties of the hydrated slag. These hydration products were analyzed using TGA, XRD, 27Al NMR, FTIR and SEM techniques. The water-to-binder ratio primarily contributes to the rate at which the conversion process occurs in the system which consequently has a direct effect on the strength derived over a period of time. Through analytical characterization of the microstructure, these hydrates and the conversion process were confirmed, revealing the initial hydrate product of ladle slag to be a metastable dicalcium aluminate octahydrate (C2AH8) which converts to a stable tricalcium aluminate hexahydrate (C3AH6) over a period of time.

Mine tailings account for most of the environmental incidents related to the extractive industry, with risks increasing due to steadily rising tonnage of low-grade ore and extreme weather events. Recycling of tailings in raw-material-intensive applications presents an interesting alternative to costly tailings management with associated restoration efforts. Chemically bonded ceramics may offer a route to upgrading mine tailings into raw materials for ceramics. In this review such chemically bonded ceramic methods that may be used to recycle mine tailings as raw materials, are reviewed while focusing in particular on two methods: 1) geopolymerization/alkali activation and 2) chemically bonded phosphate ceramics. The aim of the review is not to give exhaustive review on the wide topic, but to scope the required boundary conditions that need to be met for such utilization. According to the findings, alkali activation has been studied for 28 separate silicate minerals in the scientific literature, and presents a viable method, which is already in commercial use in calcium-rich cement-like binder applications. Phosphate bonding literature is more focused on phosphate containing minerals and waste encapsulation. Very little work has been done on low-calcium tailings utilization with either technology, and more knowledge is needed on the effect of different pre-treatment methods to increase reactivity of mine tailings in chemically bonded ceramics.

The present study valorized Finnish mining tailings waste to identify opportunities for the use of ceramics technologies. On the basis of their mineralogical and chemical contents, the five selected tailings wastes represented felsic mining tailings (FMT) rich in quartz and alkali feldspars, mining tailings dominated by Mg- and Fe-bearing minerals (MgFeMT), and mining tailings rich in carbonate minerals (CMT). Preliminary pilot studies indicated that the FMT materials are potential secondary raw materials for mullite-type ceramics. An Al additive was needed, since the Al₂O₃ content of the studied tailings was too low for mullitization. In addition, carbonate-bearing tailings with Ca silicates can be applicable for chemically bonded phosphate ceramic (CBPC) synthesis. Based on a literature review, FMT are viable source materials for the production of geopolymers, but a high initial Si:Al ratio (in quartz-rich FMT) may lead to partial geopolymerization. Preliminary results from the geopolymerization of pre-heated phlogopite mica mixed with metakaolin gave promising findings, with the formation of a geopolymer having good compressive strength. The findings support the viability of MgFeMT materials rich in phlogopite mica for the production of alkali-activated ceramics

Alkali-activated materials (AAMs), sometimes called geopolymers, have wide industrial relevance and are produced through alkaline activation of alumina and silica-rich precursors, including industrial side streams. It has been observed that MgO content in AAMs results in improved mechanical properties. However, most of the suitable MgO sources are either prohibitively expensive or carbonate-based, which leads to higher CO 2 emissions. Phlogopite is an attractive source of MgO as it is carbonate-free and locally abundant. Besides MgO, phlogopite also contains significant quantities of silica and alumina, making it a viable candidate for alkali activation. However, an alkaline solubility test in NaOH revealed phlogopite to be highly inert, with both silicon (Si) and aluminum (Al) solubility at around 1 wt% of the original material. In this work, thermal treatment was considered to improve the alkali activation potential of phlogopite. Thermal treatment was found to be successful; the resulting glassy material showed 45% Si and 33% Al release into the solution, on a par with highly soluble metakaolin (26% Si and 40% Al). During the solubility test, significant quantities of magnesium and iron were also released but they did not stay in the solution. Rather, they formed precipitated products, the main one of which was meixnerite (Mg 6 Al 2 (OH) 18 ·4H 2 O), a hydrotalcite-like compound. The resulting alkali-soluble glass with phlogopite chemical composition can be used as a carbonate-free source of magnesium in alkali activation purposes. However, any commercial application should allow for due consideration of cost.

The main objective of this paper was to investigate the alkali activation of mine tailings (MT) after mechanochemical activation and the effect of metakaolin (MK) addition. Finnish mica-rich tailings from a phosphate mine were studied as precursors for alkali-activated materials (AAM) with a potential application as a substitute for ordinary Portland cement (OPC). The principal physical properties (water absorption, apparent porosity and unconfined compressive strength) were measured for samples containing 30% to 70% tailings. Zeolite phases such as natrolite and cancrinite were observed and the formation of C-(N)-A-S-H1 and N-A-S-H gels was identified by XRD, DRIFT, FESEM-EDS and NMR technologies. A life cycle assessment (LCA) was conducted on specimens in comparison to OPC. This work indicated that phosphate MT can be recycled through alkali activation with lower CO2 emission compared to all-metakaolin geopolymers and that the binder phase formed at the most promising tailings contents (60– 70%) was C-(N)-A-S-H gel. Post-print / Final draft

Alkali-activated materials (AAMs), and geopolymers as their subgroup, are a valuable addition to the building materials with lower carbon footprints. Porous AAMs have promising performance, unique properties, and their carbon emissions are low due to the use of industrial wastes as raw materials. Porous AAMs can be prepared by several different methods such as direct foaming, sacrificial filler method, and 3D printing. Pore size plays a major role in defining, for instance, mechanical, thermal insulation, acoustic, and permeability properties. Strength improvement with a high-temperature exposure of the AAM makes it an excellent material for fireproofing and refractory linings compared to the conventional foam concrete made of Portland cement. The low thermal conductivity and high sound absorption capacity of the porous material is utilized for its application in insulation purposes. AAMs are now quickly progressing in the construction and environmental applications of the civil engineering sector. The development of foam with precise properties to satisfy the requirement for this specific application will open new market opportunities. This chapter covers the different preparation methods of porous AAMs, their characterization techniques, properties and functional relations, and applications in civil engineering.

Geopolymers have not been extensively employed as catalytic materials despite of their zeolite-resembling Si–Al structure. Geopolymerization offers a novel way for preparation of catalysts and possibility to use waste or industrial side-stream derived raw material as a resource for catalyst manufacturing. This work concentrates on metakaolin-based geopolymer materials that were prepared, characterized and tested as alternative environmentally benign catalyst supports for the oxidation of dichloromethane. The geopolymers with the Si/Al ratio of 1.5 were modified with HCl to increase their specific surface area, which is important in catalytic applications. Significant increase in specific surface areas was achieved via leaching of Na and Al from the geopolymer structure. Highest specific surface areas achieved for calcined geopolymers were over 500 m2g-1. Use of acid concentrations higher than 1 M led to the dehydroxylation of the geopolymer. Dehydroxylation decreased the total acidity of geopolymer through the loss of the Bronsted acid sites, which are responsible for the adsorption of dichloromethane in the beginning of the catalytic reaction. Absence of Bronsted acid sites was observed by the formation of CH2O as the only reaction intermediate. The best result in the dichloromethane oxidation was found with the geopolymer treated with 1 M HCl. Without using any additional active sites, the maximum dichloromethane conversion of 90% was reached at 525 °C with the maximum HCl yield of 83%. This result indicates the good potential of modified geopolymers to be used as catalyst supports in environmental applications.

The retardant effects of citric acid on the properties of ettringite binders are not yet fully understood. This investigation provides insights into the effects of citric acid on both the fresh and hardened state properties of the binder produced from the hydration between ladle slag and gypsum (LSG). The results revealed that LSG's initial setting time could be controlled via different citric acid contents and could range from 20 min to 2 h. Citric acid is effective at relatively high dosages; in its absence, ettringite formed almost immediately directly following exposure to water. The presence of citric acid alters the hydration reactions in LSG. AFm was found to be one of main hydration products; citric acid promoted the conversion from ettringite to monosulfate, detected by using solid-state 27Al magic-angle spinning nuclear magnetic resonance spectroscopy. In addition, citric acid increased the compressive strength of LSG mortars by up to 45%. This work was done as part of the FLOW project (project number 8904/31/2017) funded by Business Finland in the ERA-MIN 2 Innovation program (EU Horizon 2020 program) and industrial partners including SSAB Europe Oy, Saint-Gobain Finland Oy, Kiertokaari Oy, and Destaclean Oy. The authors appreciate support from Prof. Yiannis Pontikes (KU Leuven, Belgium) for in situ XRD measurements and Samppa Hyvarinen for lab work. Hoang Nguyen gratefully acknowledges financial support from the Tauno Tonning Research Foundation. A.M.K. and V.-V.T. acknowledge financial support from the Kvantum Institute (University of Oulu) and the Academy of Finland (grant numbers 289649 and 294027).

Use of mine tailings as an aluminosilicate precursor in alkali activation is becoming an interesting alternative to manage the high-volume of waste generated from mining industries. However, very few tailings have so far been studied for their mineralogical properties and alkali activation potential. This study aims at understanding the ability of mine tailings from phosphate, kaolinite and lithium mines for their efficient participation in alkali activation. Biotite, muscovite, kaolinite, albite, and quartz were found to be the major minerals present in them. The impact of variation in mineralogy on silica and alumina solubility of these tailings was analyzed. The solubility was found to be high in impure kaolinite compared to the other two. Effectiveness of thermal treatment (750 °C and 900 °C) on improving the reactivity of these tailings in alkaline condition was also investigated. It was observed from the results that the effect of thermal treatment on the crystalline structure and solubility of an aluminosilicate material mainly depends on the mineral structure of the material, as well as the treatment temperature. Interestingly, thermal treatment reduced the solubility of lithium tailings with albite and quartz mineral. Effort has been made to relate the strength attained by alkali activation of mine tailings to their solubility values. However, despite of the higher solubility offered by impure kaolinite, phosphate tailings gives the maximum strength improvement by 62%. This can be due to the presence of calcium compounds in phosphate tailings that resulted in additional hydration products.

Sodium silicate powders with different SiO2/Na2O (silica modulus) were characterized by solubility rate, pH, and chemical structure (by 29Si MAS-NMR) and compared in the preparation of one-part (or dry-mix) alkali-activated blast furnace slag mortar. The low SiO2/Na2O indicated the beneficial presence of less-polymerized silica (Q1 and Q2 Si environments) and thus faster dissolution. Consequently, using sodium silicates with SiO2/Na2O of 0.9, 2.1, and 3.4 resulted 28 d compressive strengths of 103, 80, and 2 MPa, respectively, with increasing setting time and decreasing heat release in isothermal calorimetry. Adjustment of activator SiO2/Na2O from 2.1 or 3.4 to 0.9 by adding NaOH powder resulted increased or decreased mechanical properties of mortar, respectively, depending on the initial silica modulus. These properties were not, however, similar to those obtained with sodium silicate having SiO2/Na2O of 0.9 originally. Depending on the case, the added NaOH can be consumed for dissolving sodium silicate activator, slag, or the forming (C,N)-(A)-S-H gel.

Gold mining produces hazardous tailings wastes with elevated sulfur content and high levels of heavy metals including oxyanion elements such as V and As. This research investigated activation of these tailings with calcium hydroxide and sodium hydroxide/sodium silicate as a way to stabilize the material and limit leaching of harmful components. The effects of thermal treatment on the reactivity of the tailings and the use of different activating solutions on the physical properties, microstructure and leaching of harmful components are reported. The effect of adding ground granulated blast furnace slag to the tailings is also assessed. The use of 5 wt % Ca(OH)2 activating solution produces optimum performance increasing the immobilization efficiency of sulfates, arsenic and the other harmful elements. Heat-treating mine tailings at 900 °C slightly improves the reactivity but did not improved the immobilization efficiency. Microstructural analysis by TEM and XRD confirmed that stabilization is based on calcium sulfate and/or ettringite formation during alkali-activation. All materials achieved reasonable compressive strength after 28 days of curing and the potential for using alkali activation as a method to treat tailings from mining is discussed.

Geopolymers are emerging construction materials with lower carbon dioxide emissions compared to the conventional cementitious materials. The knowledge of the curing process and the related pore structures are important for optimizing the properties of these materials for different applications. The curing process and final pore structure are sensitive to the amount of used water, however the specifics are unclear. The curing process and pore structures of metakaolin-based geopolymers with a narrow water-to-solid (w/s) ratio (0.59–0.66) were monitored by nuclear magnetic resonance (NMR) relaxometry and cryoporometry. The 14-day curing process was investigated by monitoring the change of T2 and T1 relaxation times and water signal intensity. After the curing, the pore structures were characterized by 2D T1-T2 correlation and T2-T2 exchange measurements of absorbed water. The pore size distributions (PSDs) were measured with NMR cryoporometry and compared to nitrogen physisorption and mercury intrusion porosimetry (MIP) results. We found that the relaxation times decreased as the pore structure of the geopolymers matured during the curing while the dissolution and the condensation periods of the curing were distinguished by the changes in signal amplitude reflecting the proton density. After the curing, three distinct pore sizes and connectivity between pores were identified from T1-T2 and T2-T2 spectra. Their PSDs were measured, and they were found to correspond to two different pore sizes originating from the arrangement of clusters and defective pores. In the narrow w/s ratio (0.59–0.66), the curing times were the same for all samples when cured at 24 °C while the pore sizes were observed to increase as a function of the w/s ratio.