Alkali-activated Cement Research Articles

Functionalizing heavy metal contained incinerated sewage sludge ash in recycled glass-based alkali-activated materials for sewer environment

This study evaluates the performance of alkali-activated cement (AAC) mortars in an artificial sewage environment. The mortars, initially prepared with waste glass powder (GP) and ground granulated blast furnace slag (GGBS) in a 50:50 mass ratio, were modified by replacing 10 wt% of GGBS with incinerated sewage sludge ash (ISSA) with the goal of offering a biocidal effect. Comparisons were made with calcium aluminate cement (CAC), metakaolin (MK), and MK combined with zinc ferrite nanoparticles, each at a similar GGBS replacement level. The results showed that only incorporating CAC improved the strength development, achieving compressive and flexural strengths of 62.7 MPa and 7.4 MPa, respectively, at 28 days, while introducing ISSA or MK reduced the compressive strength to 47 MPa and flexural strength to 4.5 MPa. Although heavy metal ions from ISSA or zinc ferrite nanoparticles minimized biofilm thickness, they could not compensate for the reduced strength and increased alkalis leaching. Among all the tested mixtures, the 50GP40GGBS10CAC mixture exhibited superior biogenic acid resistance, possibly due to its Al-rich C-N-A-S-H gel phases (Ca/Si = 0.4, Na/Al = 0.8, Si/Al = 3.4) and refined pore structure (porosity = 3.4 %), making it the most microbial acid-resistant option for sewer rehabilitation.

The formation of CaCO3-based binder by carbonating high-dosage Ca(OH)2 + slag + NaHCO3 (HCHSN) cement paste

Normally, carbonation can cause the decalcification of C-(A)-S-H gel of alkali-activated cement and the degradation of mechanical properties. While, we propose another possibility to form CaCO3-based binder by carbonating the alkali-activated slag cement of high-dosage Ca(OH)2 (30%) + slag (70%) + NaHCO3 (5.11% by weight of Ca(OH)2 and slag) (HCHSN) in this study. The results supported that the compressive strength and volume stability of HCHSN cement paste can be improved by the carbonation curing and the carbonated HCHSN cement paste could reach a maximum compressive strength of 32.4MPa. According to the micro-analysis of XRD, TGA, FTIR, 1H NMR, BSE and SEM, the carbonated HCHSN cement paste was developed into a CaCO3-based binder with a CaCO3 content approaching 60% (based on the mass of the samples heated to 800℃). NaHCO3 played a key role in the formation of the CaCO3-based binder, which not only accelerated the carbonation rate, but also promoted the carbonation of slag. The eco-efficiency assessment showed that compared to the production of 12.5kg CO2 /MPa/t from carbonated ordinary Portland cement, the carbonated HCHSN cement paste only produced 3.5kg CO2 /MPa/t, making it a very green CaCO3-based cementitious materials.

Alkaline activation via in-situ caustification of one-part binders of composite precursors of waste glass and limestone

Mixtures of powders of waste glass (WG), limestone (LS), Na2CO3 and CaO were used to formulate novel one-part in situ alkali-activated cement (WG-AAC). The in-situ interaction Na2CO3-CaO-H2O promoted the formation of CaCO3 and NaOH, which promoted the WG and LS dissolution and influenced the micro- and molecular features of the resulting cementitious products. Pastes and mortars developed 1-year strengths of up to 29 MPa and were stable underwater. Characterization by XRD, SEM, EDS, and 29Si-NMR indicated that a Na2CO3:CaO ratio close to 1:1 resulted in polymerized C-S-H, CaCO3, silica gel, and Ca-modified silica gel, which were intimately intermixed and possibly crosslinked through Q3 bonds. Such phases interacted synergistically improving the underwater stability of the WG-AAC, indicating that in-situ caustification is a suitable and practical alkaline activation for SiO2-rich precursors.

Mechanical Properties and Microstructure of Alkali-Activated Cements with Granulated Blast Furnace Slag, Fly Ash and Desert Sand

In this study, desert sand was used as supplementary materials in alkali-activated cements (AAC) with granulated blast furnace slag (GBFS) and fly ash (FA). For the first time, a systematic investigation was conducted on the effects of various treatment methods and contents of desert sand on the strength and microstructure of AAC. This study also analyzed the X-ray diffractometer (XRD), Scanning Electron Microscopy-Energy Dispersive X-ray Microanalysis (SEM-EDX), Mercury Intrusion Porosimetry (MIP), pH values, and Fourier-transform infrared spectroscopy (FT-IR) properties of AAC pastes containing differently treated desert sand to uncover the mechanisms by which these treatments and dosages influence mechanical properties of AAC. Untreated desert sand (DS), temperature-treated desert sand (DS-T), and ground desert sand for two different durations (20 mins and 30 mins) all exhibited some pozzolanic activity but primarily acted as fillers in the AAC pastes. Among the samples, DS-T demonstrated the highest pozzolanic activity, though it was still less than that of fly ash (FA). The optimal dosage for the modified desert sands was determined to be 10%. However, The optimal dosage of different modified desert sands is 10%. The flexural strength of DS-G30-10 reaches 6.62 MPa and the compressive strength reaches 72.3 MPa, showing the best comprehensive mechanical properties.

The Effect of Fiber Type on The Shear Capacity of Beams Manufactured By Using Geopolymer Concrete Based on Fly Ash

Ordinary Portland cement is currently generally used cementitious material in the construction industry. However, it has significant drawbacks as it not only depletes natural resources but also releases a substantial amount of carbon dioxide during its production process. On the other hand, alkali-activated cement is an alternative option that is derived from raw materials like slag, fly ash, and metakaolin, which contain silicon dioxide (SiO2) and aluminum oxide (Al2O3). This study investigates the shear capacity of fibre-reinforced geopolymer concrete (GPC) beams under shear loads. In the study, the shear behavior of beams produced from fly ash-based geopolymer of three different fiber types was determined by applying a three-point shear test. Four beams of 100x100x400 mm dimensions were produced: reference, steel fiber, basalt fiber and glass fiber. The results showed that using steel fiber has the greatest impact on shear capacity. In addition, the shear capacity of fibrous samples is greater than the shear capacity of the reference sample. The steel fiber sample has 203% more shear capacity than the reference sample.

Bond between alkali-activated steel slag/fly ash lightweight mortar and concrete substrates: Strength and microscopic interactions

The fire-retardant lightweight mortar spalling from the tunnel lining substrates can threaten the safety of vehicles. The use of steel slag (SS) in alkali-activated cement can reduce the carbon emission and cost of lightweight mortar. The effects of SS on the bond strength and the microstructure of the interface between alkali-activated SS/fly ash (FA) lightweight mortar (ASFm) and concrete substrates was studied. The SS contents, namely, the mass ratio of SS to the summation of FA and SS, were 0 %, 20 %, 40 %, 60 %, and 80 %. The properties of ASFm, including compressive strength, fire resistance and bond strength, were studied. Results demonstrated that the bond strength of ASFm increases and then decreases with the increase in SS content. The highest bond strength of 0.65 MPa was obtained at 40 % SS content. Bond strength was determined by the pore structure and micromechanical properties of the matrix. When the SS content was increased from 0 % to 40 %, the content of C-A-S-H gel and C-N-A-S-H gel contents increased, and the porosity was reduced; hence, the bond strength of ASFm became larger. When the SS content increased from 40 % to 80 %, SS acted as an inhibitor, which reduced the micromechanical properties and increased the porosity of ASFm; therefore, the bond strength of ASFm decreased. This achievement provides an alternative way for the application of SS in tunnels.

Response Surface Design Models to Predict the Strength of Iron Tailings Stabilized with an Alkali-Activated Cement

Tailing storage facilities are very complex structures whose failure generally leads to catastrophic consequences in terms of casualties, serious environmental impacts on local biodiversity, and disruptions in the mineral supply. For this reason, structures at risk must be reinforced or decommissioned. One possible option is its reinforcement with compacted filtered tailings stabilized with binders. Alkali-activated binders provide a more sustainable solution than ordinary Portland cement but require an optimization of the tailing–binder mixture, which, in some cases, can lead to a substantial experimental effort. Statistical models have been used to reduce the number of those experiments, but a rational design methodology is still lacking. This methodology to define the right mixture for a required strength should consider both the mixture components and in situ conditions. In this paper, response surface methods were used to plan and interpret unconfined compression strength test results on an iron tailing stabilized with alkali-activated binders. It was concluded that the fly ash content was the most important parameter, followed by the liquid content and sodium hydroxide concentration. From the obtained results, several statistical models were defined and compared according to the definition of a strength prediction model based on a mixture index parameter. It was interesting to observe that models with the porosity cement index still provide reasonable adjustment even when different tailings’ water contents are considered.

Design and evaluation of alkali-activated slag-calcined coal gangue cement and the shrinkage control by calcium carbonate whisker

The rapid solidification and significant shrinkage of alkali-activated slag cement are key issues that restrict its practical engineering application. This paper explores the composition design of alkali-activated cements (AAC) with slow coagulation and shrinkage reduction. This paper adjusts the proportion of slag (SG) and calcined coal gangue powder (CCGP), regulates the content of Na2O·2.4SiO2-NaOH-Na2CO3 ternary activator components, and uses calcium carbonate whiskers (CW) instead of SG to prepare AAC with slow coagulation and shrinkage reduction. When the activator is composed of (66 %) Na2O·2.4 SiO2-(2 %) NaOH-(32 %) Na2CO3 mixed composition, the CO32- and Ca2+ in the system react preferentially to produce CaCO3. The decrease of Ca2+ concentration delays the formation of C-(A)-S-H, resulting in the initial and final setting time of AAC reaching 334 min and 346 min, respectively. When the CW substitution rate is 3 %, the 28d compressive strength of AAC reaches 102.2 MPa. The 49d drying shrinkage of the AAC is 7020μm/m and the 49d autogenous shrinkage is 2387μm/m. This is attributed to the combined effect of enhancement mechanisms such as whisker bridging, crack deflection, whisker pullout, whisker–matrix coalition pullout and whisker breakage. This study establishes the relationship between the composition and performance of high performance AAC, which is significance for the resource utilization of coal gangue and the practical engineering application of AAC.

Basic oxygen furnace (BOF) slag as an additive in sodium carbonate-activated slag cements

Basic oxygen furnace slag (BOFS) is a high-volume waste resulting from the production of steel from pig iron. Due to its high free lime content, BOFS is difficult to recycle and/or include into conventional cement systems. Alkali-activation technology offers a pathway to transform industrial wastes such as BOFS into low-carbon cements. Alternative precursors for cement systems are needed as the reliance on commonly used materials like ground granulated blast furnace slag (GGBFS) is becoming unsustainable due to decreasing availability. This study investigates alkali-activated cements incorporating 20 and 30 wt.% of naturally weathered BOFS as a replacement for GGBFS, in both sodium silicate- and sodium carbonate-activated systems. A fraction of BOFS subject to mechanical activation is compared against the untreated BOFS in the 20 wt.% systems. It is observed that in naturally weathered BOFS, a significant portion of the free-lime is found to convert to portlandite, which accelerates alkali-activation kinetics. In sodium silicate-activated systems, the high pH of the activator results in incomplete reaction of the portlandite present in BOFS. The sodium carbonate-activated system shows near complete conversion of portlandite, causing an acceleration in the kinetics of reaction, setting, and hardening. These findings confirm the viability of sodium carbonate activated GGBFS-based systems with only a minor loss in strength properties. BOFS can be utilised as a valuable cement additive for the production of sustainable alkali-activated cements utilising sodium carbonate as a less carbon-intensive activator solution than the more commonly used sodium silicate. Mechanical activation of BOFS offers further optimisation potential for alkali-activation.

Soil improved with a hybrid alkali-activated cement from waste stone wool and OPC

The use of OPC as a construction material is currently being reconsidered owing to the generation of greenhouse gases during production. Geopolymers or alkali-activated cement (AAC) have been proposed as partial replacements because of their excellent chemical and mechanical properties, which are equal to or superior to those of OPC. The use of these alkaline types of cement in soil stabilization has also gained significant interest in the academic community because of the possibility of it being derived from industrial waste. In this study, clay soil stabilized with AAC using waste stone wool fiber (SW) as a precursor and stabilized with hybrid alkali-activated cement (HAAC) using SW and OPC was prepared and subsequently evaluated mechanically and chemically after 28 days of curing. The results showed a significant increase in soil strength with both stabilization processes. The maximum achieved unconfined compressive strength (UCS) in the soil stabilized with AAC was 0.9 MPa (15 % SW), while the strength achieved with HAAC was 1.7 MPa (10.5 % SW - 4.5 % OPC). The California Bearing Ratio (CBR) of the latter combination was also determined, finding a value of 133 %, well above that of the soil without treatment (3.32 %). Through XRD, the A-type zeolite was identified as a product of the alkaline reaction, whereas the formation of N-A-S-H and C-A-S-H gels was observed via SEM. EDS mapping showed an increase in the atomic percentages of Si and Al in the soil specimens with HAAC, indicating the formation of Si-O-Si and Si-O-Al bonds. In addition to the potential application of this material in civil infrastructure related to soils (e.g., embankments and wall fillings), a sustainable construction material using industrial waste SW with a lower percentage of OPC is proposed.

Long-term performance: strength and metal encapsulation in alkali-activated iron ore tailings.

Understanding the strength behavior and leaching characteristics of mining tailings stabilized with alkali-activated cements in the short, medium, and long term is crucial for the feasibility of material applications. In this context, this study assessed the stabilization/solidification of iron ore tailings (IOT) using alkali-activated binder (AAB) composed of sugarcane bagasse ash and eggshell lime at curing times of 7, 28, 60, 90, 180, and 365days. Additionally, leaching tests were conducted, along with the examination of possible changes in the chemical and mineralogical composition resulting from exposure to acidic environments. Tests included unconfined compression strength (UCS), leaching, X-ray diffraction, and Fourier-transform infrared spectroscopy for the IOT-AAB mixtures. The highest increase in UCS was observed between 7 and 60days, reaching 6.47MPa, with minimal variation thereafter. The AAB-bonded IOT exhibited no metal toxicity over time. Elements Ba, Mn, Pb, and Zn present in IOT and ash were encapsulated in the cemented matrix, with complete encapsulation of all metals observed from 90days of curing time. The mineralogy of the stabilized/solidified tailings showed no changes resulting from leaching tests. Characteristic bands associated with the presence of N-A-S-H gel were identified in both pre-leaching and post-leaching samples for all curing times analyzed. Exposure to acidic environments altered bands related to carbonate bonds formed in the IOT-AAB mixture.

Investigation of shrinkage mechanism of alkali-activated slag

Slag is a highly active waste product that can be added to alkali-activated cement to improve their mechanical properties, but also creates significant shrinkage, which limits its usefulness. This study examines the reasons behind the shrinkage of alkali-activated slag (AAS). The research uses a comprehensive approach that includes linear shrinkage testing, comparative chemical analysis, microscopic structural characterization, internal relative humidity evaluations, pore size distribution assessments, and nanoindentation testing. The results show that AAS has more chemical shrinkage, self-drying shrinkage, and drying shrinkage than ordinary Portland cement. AAS’s shrinkage deformation increases with variations in the activator modulus. Chemical reactions that produce aluminosilicate gel with smaller particle sizes and lower bound water are the primary factors contributing to chemical shrinkage in AAS. The high self-drying and drying shrinkage of AAS can be attributed to several factors: AAS experiences a more rapid decrease in internal humidity during the early curing stages, AAS materials typically exhibit smaller most probable pore sizes, and hardened AAS products tend to have a lower creep modulus. The addition of oil shale semi-coke (OSS) to AAS can modify the composition and microstructure of the reaction products, resulting in an increase in porous reaction products and ultimately reducing shrinkage. This study's findings are significant for understanding the causes and potential solutions for alkali-activated cement shrinkage issues.

Mechanochemical activation of waste glass in alkaline composite cements with blastfurnace slag: A sustainable approach to recycling

This study investigates alkali-activated cements incorporating blast furnace slag and urban waste glass across varying slag:glass ratios (100:0, 25:75, 75:25, 0:100). Activation with 4 % and 12%Na2Oeq, coupled with two curing regimes (24h at 60 °C, followed by either 60 °C or 20 °C for 28 days), was explored. Prior to each formulation, part of the waste glass underwent mechanochemical ball milling with the required water and alkalis, to enhance the glass reactivity and to pre-dissolve SiO2 and other species to obtain a waterglass-like material in an environmentally friendly manner. Optimal strengths were achieved for slag binders (27 MPa) with 4%Na2O and 20 °C curing, while waste glass binders (48 MPa) required 12%Na2O and 60 °C. Composite formed cementitious products of CaO-(Al2O3)–SiO2–H2O gel, calcite, and hydrotalcite as reaction products, while 100 % waste glass binders displayed cementitious products of CaO–SiO2–H2O intermixed with silica gel. This approach holds promise for reducing environmental impact and promoting the efficient widespread and straightforward reuse of urban waste glass in construction materials.

Rainfall-induced wind erosion in soils stabilized with alkali-activated waste materials

This study evaluates the efficacy of sustainable erosion control using slag-based alkali-activated cement crusts under varying rainfall and wind conditions. The rainfall intensities ranged from 30 mm/h to 120 mm/h, with durations ranging from 15 min to 90 min, and crust slopes of ∼2° (gentle) and 30° (steep). Wind tunnel experiments were conducted at wind velocities of 14 m/s, 21 m/s, and 28 m/s to investigate post-rainfall wind erodibility, along with changes in crust strength and microstructure analysis. The findings show the development of hydrated cementitious phases in alkali-activated material, which form around and between the particles during the alkaline activation process. Alkali-activated cement crusts significantly reduced erosion caused by rainfall and subsequent wind by several orders of magnitude. At the highest rainfall intensity of 120 mm/h, rainfall erosion was measured to be 1654.81 kg/m2 for untreated samples and 0.89 kg/m2 for treated samples, demonstrating a substantial 99.95% reduction in erosion due to the treatment. Similarly, at the highest wind speed tested, wind erosion was 122.75 kg/m2 for untreated samples and 0.095 kg/m2 for treated samples, indicating a significant 99.92% reduction in erosion due to the formation of an alkali-activated cement crust on the soil surface. However, exposure of the samples to 120 mm/h rainfall for 90 min resulted in a 5.2-fold increase in wind erosion compared to pre-rainfall conditions. Similarly, penetrometer results indicated a 37%–54% reduction in post-rainfall surface strength.

Micromechanical and chemical characteristics of interfacial transition zone in alkali-activated slag concrete containing lightweight iron-rich aggregates

This study explored the time-varying alkali-activation effects of the lightweight aggregates (LWA) on the interfacial transition zone (ITZ) of the alkali-activated slag concrete with different curing ages, molar ratios, and alkali concentrations from 28 to 300 d. The improved micromechanical performance of the ITZ at 28 d stemmed from the early-age internal curing effect of the porous LWA. However, the post-28 d internal curing effect diminished, with the alkali-activation dominating the performance of the ITZ from 28 to 300 d. Although alkali-activated cement possessed early strength characteristics, the deconvolved phase results illustrated that alkali activation persisted in the ITZ between the LWA and cement from 28 to 300 d, leading to a high proportion of calcium silica aluminate hydrate. As a marker, Fe from the lightweight iron-rich aggregates mitigated into the alkali-activated cement, demonstrating the alkali-activated reaction between the LWA and alkali-activated slag matrix. Molecular dynamics simulations further characterized that the low content of Fe did not decrease the overall strength of the ITZ. The interfacial interaction energy revealed the alkali-activation between the LWA and cement compensated for the weakening of mechanical properties caused by Fe ions on the ITZ.

One-part alkali-activated GGBFS as a cement for enhancing compacted filtered iron ore tailings disposal by stacking

Brazil is one of the top world iron ore producers. However, it implies the generation of millions of tons of iron ore tailings (IOTs). Dewatering technologies now permit the obtainment of a compactable geomaterial rather than the slurry consistency tailings that were commonly stored in impoundments. Thus, this filtered compacted geomaterial can be stacked in piles. In this regard, the incorporation of small amounts of cement into the filtered tailings has the potential to strengthen the geomaterial. By using alkali-activated binders, strengthening the IOTs’ mechanical properties can be achieved with minimum environmental drawbacks. Accordingly, the present study evaluates the strength, mineralogy, and microstructure of compacted iron ore tailings-binder blends. A one-part alkali-activated cement (AAC) composed of ground granulated blast furnace slag (a residue of steel industry), sodium silicate, and sodium hydroxide was used, highlighting the circular economy appeal of this cement. A response surface approach was used in the definition of this cement’s composition. As well, tests using a commercially available high early-strength Portland cement were conducted. The optimized AAC outperformed the early strength Portland cement regardless of the test conditions, associated with the formation of a more developed cementitious matrix (C-S-H and C-A-S-H gel of amorphous structure).

Structuration and yield strength characterization of hybrid alkali-activated cement composites (HACC) for ultra-rapid 3D construction printing

This study investigates the critical time-dependent rheological properties, including structuration rate and yield stress, of hybrid alkali-activated cement composites (HACC). HACC, a blend of geopolymer and cement paste, is examined to evaluate its suitability for ultra-rapid 3D construction printing (3DCP), which refers to a material’s ability to attain rapid structuration and buildability within 5–10 min after mixing, essential for additive manufacturing of 3D structures. The investigation extends to the impact of filler materials like silica sand and PVA fibers on HACC’s rapid structuration. Vicat needle, fast- and slow-penetration resistance measurements indicate that setting time increases with decreasing the Silicon/Aluminum (S/A) molar ratio and the addition of silica sand. Conversely, the addition of fibers reduces setting time while enhancing yield strength. Specifically, HACC mixtures with 0.5% and 1% PVA fiber additions, alongside combined sand (30%, 40%) and fiber (0.5%) mixtures, demonstrate ultra-rapid setting behavior within 3–5 min. Notably, mixtures with 40% silica sand and 0.5% PVA fiber exhibit highest yield strength development, i.e., 14 MPa at 12 min. Remarkably, incorporating 1% fibers into the HACC mixture yields the highest 28-day compressive strength (∼80 MPa) and flexural strength (∼11 MPa). The synergistic interplay between geopolymer and cement facilitates rapid setting time and high early-age strength development in HACC mixtures. The varying effects of silica sand and PVA fiber on setting time and yield strength provide opportunities for designing suitable structuration profiles. These findings underscore the exceptional rapid setting, structuration, and mechanical properties of HACC, positioning it as a promising material for ultra-rapid 3D construction printing.

Parameters controlling the expansive behavior of bentonite-kaolin mixtures stabilized with alkali-activated waste

Expansive soils can cause large-scale damage to the infrastructure. Soil stabilization with Portland cement and lime has been widely utilized as a solution to this problem. However, these stabilizers are non-renewable and energy-intensive. Alkali-activated binders are alternatives with lower carbon dioxide emissions. This research evaluated an expansive soil stabilization with an alkali-activated binder produced from sugarcane bagasse ash (SCBA), hydrated eggshell lime (HEL) and sodium hydroxide (NaOH). Free-swelling tests alongside a statistical analysis evaluated the influence of dry unit weight (12.5 and 14.5 kN/m3), binder (4 and 10%) and moisture content (19.7 and 24.7%) and curing time (0 and 7 days) on the stabilized mixtures. A four factors factorial design with duplicates and central points was outlined. To better understand the NaOH and SCBA influence over the soil expansion additional tests were performed. In general, an increase on the studied factors reduced swelling, especially binder content. However, the alkali-activated cement presented no clear correlation between higher density and higher expansion. Swell reduced from 13.8% (12.5 kN/m3 and 19.7% moisture) and 8.8% (12.5 kN/m3 and 24.7% moisture) to 2.5% and 0%, respectively, after 7 days and 10% binder addition for the alkaline cement. For Portland cement, swell reduced from 13.8% (10.2 kN/m3 and 22.5% moisture) and 12.5% (10.2 kN/m3 and 27.5% moisture) to 1.8% and 1%, respectively, after 7 days and 4% binder addition. Samples containing NaOH expanded less than samples molded with only water. Finally, the alternative binder might be a viable option to replace Portland cement for expansion control.

ПЕРСПЕКТИВЫ ИСПОЛЬЗОВАНИЯ ОТХОДОВ СТРОИТЕЛЬНОЙ КЕРАМИКИ ПРИ ПРОИЗВОДСТВЕ СТРОИТЕЛЬНЫХ МАТЕРИАЛОВ

The main technological aspects of the production of building ceramics are given. Based on the analysis of literary sources, a comprehensive assessment of the feasibility of using construction ceramic waste as a secondary raw material for the production of new building materials was carried out. Based on the research of modern scientists, it has been established that the waste from the scrap of building ceramics is suitable for use as an aggregate, partial replacement of cement and a reactive additive in concretes and mortars. When using scrap of con-struction ceramics as an aggregate, it is recommended to limit the substitution of natural aggregate at the level of 20-30%, together using various additives: plasticizing and improving rheotechnological and physico-mechanical properties of concrete. Finely ground waste from brick scrap has pozzolan activity and, when used as a reactive additive or partial replacement of cement in concretes and mortars, up to 20-25% can improve the structure of cement stone, increase strength, reduce macroporosity and penetration of chloride ions, and increase sul-fate resistance. This kind of binder is prone to a later set of strength compared to Portland cement. In addition, the waste of building ceramics can be used in the production of alkali-activated cements and slag-alkali binders, as well as s raw materials for the production of new bricks or the construction of road surface bases. It has been revealed that the production of building materials and products based on con-struction ceramics waste is a promising direction for the development of construction production. It is possible not only to obtain materials of equal quality to products based on natural raw materials, but also with improved characteristics.

Alkali-activated cements based on limestone-fly ash: Effect of the MgO-NaOH activation, compressive strength and reaction products

This study investigates the effects of alkaline activation with MgO-NaOH on the compressive strength and reaction products of alkali activated cements of limestone powder (PClz) and Class C fly ash (CV). Results showed that substitutions of 25%<PClz<75% allowed 25-76 MPa at 360 days of curing, obtaining the highest strength with 25%PClz-75%CV and 50%PClz-50%CV with 10 and 12% NaOH-MgO, respectively. The results suggest that PCLz participates in hydration reactions as filler and nucleating agent while CV is the main contributor to the advance of the chemical reactions. X-ray diffraction (XRD), Thermal analysis (TA) and Scanning Electron Microscopy (SEM) indicated the formation of M-S-H, and C, N-A-S-H-type products, in addition to carbonate phases such as hydrotalcite, gaylussite, and pirssonite. Traces of unreacted MgO were not observed indicating its whole incorporation into the reaction products.