This research explores the stabilization of clay soil through the application of geopolymer binder derived from silicomanganese slag (SiMnS) and activated by sodium hydroxide (NaOH). This research aims to evaluate the effects of key parameters, including the percentage of slag, the activator-to-stabilizer ratio, and curing conditions (time and temperature), on the mechanical properties of the stabilized soil. Unconfined compressive strength (UCS) tests were conducted to assess improvements in soil strength, while scanning electron microscopy (SEM) was employed to analyze the microstructural changes and stabilization mechanisms. The results demonstrated that clay soil stabilized with SiMnS-based geopolymers exhibited significant strength enhancement. Specifically, the sample stabilized with 20% SiMnS and an activator-to-slag ratio of 1.6, cured at room temperature for 90 days, achieved a UCS of 27.03 kg & frasl;cm2. The uniaxial strength was found to be positively correlated with the SiMnS content, activator ratio, curing time, and temperature. Additionally, the strain at failure remained below 1.5% for all samples, indicating a marked improvement in soil stiffness. SEM analysis revealed that geopolymerization led to the formation of a dense matrix, enhancing soil particle bonding and overall durability. These results emphasize the potential of SiMnS-based geopolymers as a sustainable and effective soil stabilizer for geotechnical applications.
Lunar soil, as an in-situ resource, holds significant potential for constructing bases and habitats on the Moon. However, such constructions face challenges including limited mechanical strength and extreme temperature fluctuations ranging from -170 degrees C to +133 degrees C between lunar day and night. In this study, we developed a 3D-printed geopolymer derived from lunar regolith simulant with an optimized zig-zag structure, exhibiting exceptional mechanical performance and thermal stability. The designed structure achieved remarkable damage tolerance, with a compressive strength exceeding 12.6 MPa at similar to 80 vol% porosity and a fracture strain of 3.8 %. Finite element method (FEM) simulations revealed that the triangular frame and wavy interlayers enhanced both stiffness and toughness. Additionally, by incorporating strategically placed holes and extending the thermal diffusion path, we significantly improved the thermal insulation of the structure, achieving an ultralow thermal conductivity of 0.24 W/(m K). Furthermore, an iron-free geopolymer coating reduced overheating under sunlight by 51.5 degrees C, underscoring the material's potential for space applications.
This study developed a novel geopolymer (RM-SGP) using industrial solid wastes red mud and slag activated by sodium silicate, aiming to remediate composite heavy metal contaminated soil. The effects of aluminosilicate component dosage, alkali equivalent, and heavy metal concentration on the unconfined compressive strength (UCS), toxicity leaching characteristics, resistivity, pH, and electrical conductivity (EC) of RM-SGP solidified composite heavy metal contaminated soil were systematically investigated. Additionally, the chemical composition and microstructural characteristics of solidified soil were analyzed using XRD, FTIR, SEM, and NMR tests to elucidate the solidification mechanisms. The results demonstrated that RM-SGP exhibited excellent solidification efficacy for composite heavy metal contaminated soil. Optimal performance occurred at 15 % aluminosilicate component dosage and 16 % alkali equivalent, achieving UCS >350 kPa and compliant heavy metal leaching (excluding Cd in high-concentration groups). Acid/alkaline leaching tests revealed distinct metal behaviors: Cu/Cd decreased progressively, while Pb initially declined then rebounded. Microstructural analysis indicated that RM-SGP generated abundant hydration products (e.g., C-A-S-H, N-A-S-H gels), which acted as cementitious substances wrapping soil particles and filling and connecting pores, thereby increasing the soil's compactness and improving the solidification effect. Furthermore, heavy metal ions were solidified through adsorption, encapsulation, precipitation, ion exchange, and covalent bond et al., transforming their active states into less bioavailable forms, proving novel insights into the remediation of composite heavy metal contaminated soils and the resource utilization of industrial solid wastes.
The paper investigates the effect of curing conditions on the properties of laterite soil-based geopolymer cement. In the experimental testing, calcined laterite soil was used as a solid precursor in the preparation of geopolymer cement. Standard size prismatic geopolymer specimens were prepared and subjected to four curing methods, including open air curing and courses of combined open-air curing and oven curing. The prisms were tested at 3, 7, and 28 days to determine the effect of curing methods on the flexural and compressive strengths. The crushed prisms were further pulverised and analysed to investigate the microstructure, elemental composition, mineralogical phases, chemical bonding, and thermal behaviour. The findings showed that the highest strength at 28 days was obtained with the air curing method. However, the curing methods involving an oven curing course resulted in the highest early strength at 3(early strength) and 7 days.
The socio-economic growth of a nation depends heavily on the availability of adequate infrastructure, which relies on essential materials like river sand (RS) and cement. However, the rising demand for RS, combined with its excessive extraction causing ecological damage, and its increasing cost, has raised significant concerns. At the same time, the production of cement contributes significantly to environmental damage, especially through CO2 emissions. In this scenario geopolymer technology has emerged as a sustainable alternative to cement, offering environmental benefits and reducing the carbon footprint of construction materials. This study investigates the impact of replacing RS with copper slag (CS) and laterite soil (LS) in geopolymer mortar (GM) on key properties such as setting time, flowability, compressive strength, and microstructure. The results showed that as LS content increased, setting time and flowability decreased considerably, while increasing CS content caused a reduction in these values. Unlike the other observed parameters, the compressive strength values showed no distinct upward or downward trend. Moreover, the microstructural analysis, including SEM, EDS, XRD, FTIR, TGA and BET, provided valuable insights to support the observed results across various mix designs. Overall, the findings highlight that optimised binary blends of CS, LS and RS not only improved the compressive strength but also enhanced the microstructural characteristics of geopolymer mortar, reinforcing their potential as sustainable and high-performance alternatives to conventional fine aggregates.
Geopolymer concrete is a promising alternative to traditional cement due to its lower carbon footprint and enhanced mechanical properties. While carbonatogenic bacteria have been widely studied in Portland cement, their role in geopolymers remains underexplored, particularly in noncalcium precipitation mechanisms. This study screened limestone quarry samples using 16S amplicon sequencing to identify potential carbonatogenic bacteria. Following isolation and precipitation analysis, Lysinibacillus fusiformis JH2 was selected and incorporated into fly ash-bottom ash-based geopolymer paste. XRD and SEM analysis revealed that microbial carbonation led to the formation of aragonite, natrite, and brucite, refining pore structures, enhancing durability, and increasing compressive strength. Incorporating JH2 endospores significantly improved early strength, achieving 17.5 MPa within 7 days, meeting Indonesian structural standards, and increasing strength by up to 166 %. Notably, bacteria remained viable and retained their ability to form endospores, opening possibilities for endospore storage in artificial aggregates for selfhealing and bio-enhanced construction materials. These findings also show a potentially novel microbial pathway for non-calcium precipitation, contributing to the faster, more sustainable enhancement of geopolymer concrete for industrial applications.
Deep soil mixing (DSM) is a widely used ground improvement method to enhance the properties of soft soils by blending them with cementitious materials to reduce settlement and form a load-bearing column within the soil. However, using cement as a binding material significantly contributes to global warming and climatic change. Moreover, there is a need to understand the dynamic behavior of the DSM-stabilized soil under traffic loading conditions. In order to address both of the difficulties, a set of 1-g physical model tests have been conducted to examine the behavior of a single geopolymer-stabilized soil column (GPSC) as a DSM column in soft soil ground treatment under static and cyclic loading. Static loading model tests were performed on the end-bearing (l/h = 1) GPSC stabilized ground with Ar of 9 %, 16 %, 25 %, and 36 % and floating GPSC stabilized ground with l/h ratio of 0.35, 0.5, and 0.75 to understand the load settlement behavior of the model ground. Under cyclic loading, the effect of Ar in end-bearing conditions and cyclic loading amplitude with different CSR was performed. Earth pressure cells were used to measure the stress distribution in the GPSC and the surrounding soil in terms of stress concentration ratio, and pore pressure transducers were used to monitor the excess pore water pressure dissipated in the surrounding soil of the GPSC during static and cyclic loading. The experimental results show that the bearing improvement ratio was 2.28, 3.74, 7.67, and 9.24 for Ar of 9 %, 16 %, 25 %, and 36 %, respectively, and was 1.49, 1.82, and 2.82 for l/h ratios of 0.35, 0.5, and 0.75 respectively. Also, the settlement induced due to cyclic loading was high under the same static and cyclic stress for all the area replacement ratios. Furthermore, the impact of cyclic loading is reduced with an increase in the area replacement ratio. Excess pore water pressure generated from static and cyclic loads was effectively decreased by installing GPSC.
In this study, ground granulated blast-furnace slag (GGBS) and fly ash (FA) were used as binders, while NaOH (NH) and Na2SiO3 (NS) served as alkali activators. Seawater (SW) was used instead of freshwater (FW) to develop a SW-GGBS-FA geopolymer for solidifying sandy soils. Geopolymer mortar specimens were tested for unconfined compressive strength (UCS) after being curing at room temperature. The results showed that the early strength of the seawater group specimens increased slowly less than that of the freshwater group specimens, while the late strength was 1.16 times higher than that of the freshwater group specimens. Factors including seawater salinity (SS), the GGBS/FA ratio, curing agent (CA) content, and the NH/ NS ratio were examined in this experiment. The results showed that the strength of the specimens was higher for SS of 1.2 %, G90:F10, CA content of 15 %, activator content was 15 %, and NH: NS of 50:50. The pore structure of the mortar specimens was analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and computerized tomography (CT), revealing the mechanisms by which various factors influenced the microstructure. XRD indicated that SW-GGBS-FA geopolymer mortar newly produced Friedel salt and calcium silicate sulfate hydrate (C-S-S-H). The microstructures observed by CT and SEM showed that the pore radius of the seawater specimens was mainly less than 10 mu m, and the maximum crack length was 92.55 mu m. The pore radius of freshwater specimens was larger than that of seawater specimens, and the largest crack was 148.44 mu m, which confirmed that Friedel salt and C-S-S-H fill the pores and increase the UCS of the specimens.
Geopolymers are recently recognized as superior sustainable alkali-activated materials (AAMs) for soil stabilization because of their strong bonding capabilities. However, the influence of freeze-thaw cycles (FTCs) on the performance of geopolymer-stabilized soils reinforced with fibers remains largely unexplored. In the current study, for the first time, the durability of polypropylene fiber (PPF) reinforced clayey soil stabilized with fly ash (FA) based geopolymer is investigated under FTCs, evaluating its performance during prolonged seasonal freezing. The effects of repeated FTCs (0, 1, 3, 6, and 12 cycles), different contents of alkali-activated FA (5 %, 10 %, and 15 %), varying PPF percentages (0 %, 0.4 %, 0.8 %, and 1.2 % with a length of 6 mm), and curing time (7 and 28 days) on the properties of stabilized samples have been determined through tests including standard Proctor compaction, unconfined compressive strength (UCS), mass loss, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and Fourier transform infrared spectroscopy (FTIR). The results revealed that a 0.4 % PPF concentration maximized strength in FA-based geopolymer samples by restricting crack propagation, irrespective of FA content, number of FTCs, or curing time. However, higher PPF contents lowered UCS values and Young's modulus due to fiber clustering and increased failure strain, respectively. Generally, an initial increase in UCS, Young's modulus, and resilience modulus (MR) of stabilized samples occurred with more FTCs because of their dense structure, delayed pore formation, and continued geopolymerization process and followed by a constant or decreasing trend in strength after 6 (or 3 in some cases) FTCs due to ice expansion in created air voids. Longer curing time resulted in denser samples with improved resistance to FTCs, especially under 12 FTCs. Moreover, samples with 10 % alkali-activated FA demonstrated the least susceptibility to FTCs. While initial FTCs caused no mass loss, subsequent cycles led to increased mass loss and remained below 2 % for all samples. Microstructural analysis results corroborated UCS test results. Although the primary chemical composition remained unchanged after 12 FTCs, these cycles induced morphological changes such as critical void formation and cracking within the gel structure. The stabilization approach proposed in this study demonstrated sustained UCS after 12 FTCs, promising reduced maintenance costs and extended service life in regions with prevalent freeze-thaw damage.
Due to the detrimental ecological impacts and the exorbitant expenses associated with the cement industry, researchers have sought to find natural, sustainable, low-carbon alternatives to Portland cement for weak soil stabilization. This research used geopolymer based on metakaolin (MK), a natural pozzolanic material with different activator concentrations (NaOH and Na2SiO3), to stabilize loose poorly graded sand soils. The research investigated the effect of different amounts of addition MK (5, 10, and 15 %) on the soil's mechanical properties. Furthermore, the effect of parameters such as the type and concentration of the alkaline solution and curing time (1, 3, and 7 days) on the unconfined compressive strength, failure strain, Young's modulus, California bearing ratio, and direct shear test were evaluated. This research also aims to measure the sub- grade reaction modulus (Ks) by developing and manufacturing a laboratory testing apparatus and steel mold to simulate the natural conditions of sandy subgrade soil obtained from performing nonrepetitive static plate load tests. Additionally, scanning electron microscopy images (SEM) and X-ray diffraction analysis (XRD) were also used to study the microstructural changes and the chemical composition of the stabilized soil samples. The results indicate that the soil samples that were stabilized with MK 10 % and NaOH had notably higher compressive strength (2936 kPa), indicating a denser and less porous structure (improved stiffness stabilized soil) in comparison to the soil samples stabilized with MK 10 % and Na2SiO3 which was (447 kPa). Ultimately, Microstructural analysis showed that, due to the addition of 10 % MK, stabilized soils have a denser and more homogeneous structure.