1. Introduction
In recent years, the resource utilization of waste materials has emerged as a critical issue [
1,
2]. By crushing and processing waste concrete, mortar, bricks, tiles, and similar materials into recycled aggregates, these can be used to completely or partially replace natural aggregates in concrete production. This recycled aggregate concrete can then be used to create artificial blocks, such as protective bricks, and can potentially be employed in load-bearing structures like beams, deep beams, and corbels [
3,
4]. Alternatively, lightweight aggregates made from solid waste such as fly ash can be used to prepare lightweight blocks or walls. The incorporation of solid waste into building materials not only consumes a large amount of industrial waste but also reduces the environmental impact, conserves land, lowers project costs, alleviates the shortage and depletion of natural sand and gravel resources, and contributes positively to ecological protection.
In addition, the rapid development of water transportation has led to extensive construction and maintenance of ports and waterways, resulting in significant volumes of dredged soil. China has become a major dredging country worldwide, with an annual production of over 1 billion cubic meters of dredging soil. Traditionally, much of this dredged soil has been discarded in deep channel waters, leading to inefficient utilization. While some dredged soil is used for land reclamation, the methods employed are often simplistic and extensive, causing a waste of soil resources and secondary pollution to the environment [
5]. Therefore, the rational, effective, and environmentally friendly utilization of dredged soil resources to play a positive role has become a new problem that urgently needs to be solved in the water transportation industry. The resource utilization of dredged soil has attracted widespread attention [
6].
The use of dredged soil in construction is primarily divided into two main approaches. The first involves the use of enhanced dredged soil in the restoration and reclamation of abandoned mines and industrial sites through landfill techniques. The second approach utilizes dredged soil as an aggregate in the manufacture of concrete blocks that possess sufficient strength for use in road construction and municipal engineering projects. Through field planting experiments, Dong et al. [
7] confirmed the practical effectiveness of utilizing dredged sediments for waste disposal through mine reclamation. Their results revealed that dredged sediments provided ample organic matter and nitrogen, resulting in enhanced plant growth and increased density of photosynthetic carbon fixation. Furthermore, Chu et al. [
8] explored the combined use of dredged river sediment, iron ore tailings, and calcium carbide slag as fill materials to tackle ground subsidence issues. They found that an optimal mix consisting of a 7:3 mass ratio of dredged river to iron ore tailings along with a cement content of 16.7% yielded the highest flowability. Li et al. [
9] conducted an extensive study on the processing of dredged sediments, which included dehydration, detoxification, and calcination to create ceramic particles. These particles were then used for backfilling and capping in dredged areas, leading to significant enhancements in bed stability and a reduction in sediment erosion by more than 70%. Additionally, the study demonstrated the effective inhibition of phosphorus release from contaminated sediments, with an inhibition efficiency of up to 80%. In another study, Yu et al. [
10] proposed a method for recycling dredged sludge by incorporating ground steel slag into the slurry. The sludge was then subjected to continuous processing through foam drying and carbonization stabilization; the maximum unconfined compressive strength of the modified soil reached 2.01 MPa, which was 8.5 times higher than the strength before carbonization stabilization. Hussain et al. [
11] explored the potential of utilizing harbor and river sediments in the experimental production of soil-cured bricks. The study utilized sediment from Dunkirk harbor in France and replicated the brick-making process on sediments from the Usamazinta River, and they compared the mechanical properties of bricks made from the two types of sediments, including tensile strength, toughness, and fiber distribution. The results indicate that the addition of natural fibers can transform earth blocks into ductile materials, enhancing the toughness of the bricks. Moreover, the tensile strength meets the minimum recommended tensile strength of 0.25 MPa. Meanwhile, Yang et al. [
12] harnessed dredged sediments as lightweight aggregates in the production of non-sintered permeable bricks. Their experiments revealed optimal performance conditions, specifically with a water-to-cement ratio of 0.34, forming pressure of 3 MPa, and porosity level of 15%. Based on the above, it is evident that the resource utilization of dredged soil primarily revolves around methods such as stabilization, solidification, and sintering to improve its properties.
Numerous studies have been conducted on the mechanical properties and solidification potential of dredged soil when used as fine aggregate in concrete, with various researchers utilizing cementitious materials to enhance its capabilities. Ponnada et al. [
13] experimented with a mixture of dredged sand and quarry dust as a partial replacement for river sand in concrete, finding that a 50% replacement dosage yielded a compressive strength of 38.7 MPa. Concurrently, Bhairappanavar et al. [
14] crafted bricks from dredged materials, assessing their compressive strength, water absorption, and freeze–thaw durability. Results showed compressive strengths ranging from 10.3 to 17.2 MPa, water absorption between 13% and 18%, and minimal weight loss of 0.1% to 0.4% after 50 freeze–thaw cycles. Xu et al. [
15] designed concrete mixtures with different dredged sand contents and subjected them to various numbers of freeze–thaw cycles to study the frost resistance and fracture behavior of dredged sand concrete. The study revealed that an augmented dredged sand content led to an improved pore structure, thereby enhancing the fracture behavior and frost resistance of the concrete. The study revealed that an augmented dredged sand content led to an improved pore structure, thereby enhancing the fracture behavior and frost resistance of the concrete. Vinothkumar et al. [
16] found that dredged marine sand performs well as a substitute for fine aggregate in concrete, improving its physical, mechanical, and mineralogical properties. The presence of calcite and calcium enhances the strength of the concrete, while silica acts as a filler material. In another approach, Huang et al. [
17] prepared high-performance concrete by substituting 25% of ordinary sand with dredged sand, which improved the concrete’s density, reduced its porosity, and enhanced the pore distribution uniformity and interface structure. Meanwhile, Lee et al. [
18] studied the influence of different mix proportions on the shrinkage behavior of lightweight dredged soil concrete at early and long-term ages. The shrinkage strain at 28 d was found to be 39% to 55% of the shrinkage strain at 210 d, indicating that the internal curing effect of lightweight aggregates delayed the onset of the acceleration period.
Despite the existing research, there remains a noticeable gap in the study of high-strength blocks using high-clay-content dredged soil as the primary material. The assurance of quality and reliability necessitates extensive experimentation coupled with effective control measures. While chemical, physical, and mechanical properties of dredged sediment blocks have been studied, the mechanisms behind the mechanical properties and microstructural characteristics, such as phase composition and pore structure, have not been thoroughly revealed. Research on different molding methods (such as compaction molding and vibration molding) and evaluations related to drying shrinkage are still relatively limited. Further research is needed to deepen our understanding of concrete preparation using dredged soil, and it will provide important scientific foundations for addressing related issues.
Dredged silt is a major type of dredged soil, characterized by small pores, poor structure, and weak permeability. Currently, there is no specialized research on the preparation of blocks using silt as a substitute for traditional sand and gravel materials. This study aims to address this gap by utilizing industrial waste materials, such as silicon aluminum compounds (e.g., fly ash) and mineral powder, to partially replace cement. Dredged silt is used as the primary raw material instead of ordinary sand and gravel to prepare artificial blocks. The mechanical properties of the silt blocks under ordinary vibration molding and semi-dry pressing molding are compared and analyzed. The study evaluates the compressive strength, splitting tensile strength, and dry shrinkage performance of the dredged silt blocks with varying cement replacement levels of fly ash and mineral powder (0%, 20%, 30%, 40%, and 50%). Additionally, micro-mechanism research such as SEM, MIP and TG-DSC is carried out, which can provide an effective way for the high-value-added utilization of dredging silt blocks and lay a foundation for the subsequent promotion and application of dredging silt blocks.
3. Results and Discussion
3.1. Influence of Different Molding Methods on Mechanical Properties of Dredged Silt Blocks
Blocks were produced using semi-dry pressing and vibration molding techniques, with a binder composition of 70% cement and 30% ground granulated blast-furnace slag (GGBS). The experimental results for the relevant mechanical properties are depicted in
Figure 4. Compared to the specimens prepared using vibration molding, the specimens prepared using the pressing method exhibits significant improvements in compressive strength and splitting tensile strength. The compressive strength and splitting tensile strength at 28 d reached 64.8 MPa and 5.6 MPa, respectively. These values denote a substantial improvement, registering remarkable increases of 110.5% and 142.8% compared to specimens prepared using vibration molding with identical mix proportions.
The preparation of ordinary concrete typically involves vibration molding, a process in which the material is liquefied under high-frequency vibration, allowing it to densely fill the mold under its own weight and external forces. This method effectively expels air between particles, resulting in a material with uniform density and reliable strength. Compression molding is the process of using mechanical force to squeeze out the air wrapped in the mixture, reducing the number and volume of pores, expelling excess water, and eliminating some micro cracks caused by chemical shrinkage of the slurry, thereby improving the compactness and strength of the block. Similarly, semi-dry compression molding utilizes mechanical force to extrude the air enclosed in the mixture, reduce the number and volume of pores, and expel excess moisture, thereby enhancing the density and strength of the block. Due to the high compressibility and difficulty in compacting the dredged mud, compression molding can significantly improve the strength of the block, especially its early strength. Additionally, it allows for immediate demolding, which accelerates the turnover rate of the grinding tool. During the process of pressing molding, applying a significant amount of pressure can result in tighter contact and denser arrangement of the dredged silt particles, increasing both the frictional and cohesive forces between them. Moreover, OPC and GGBS, serving as binders, facilitate the bonding of these particles, further enhancing the block’s integrity. For the dredged silt used in this study, the presence of sand particles within the silt provides a skeletal support during block preparation. Compared to the dredging soil mainly composed of clay particles, it is easier to play a role in particle grading such as particle matching and embedding, thereby improving the strength and durability of the blocks. Consequently, the strength of dredged silt blocks can be significantly improved through the combined effects of mechanical force, particle size distribution, and hydration.
The block pressing production process mainly includes weighing, dry mixing, wet mixing, compression molding, demolding, curing and other processes. The prepared block can be demolded immediately, simplifying the process and accelerating mold turnover. The specific pressing production process of dredging soil blocks is shown in
Figure 5.
3.2. Influence of Different Proportions of Fly Ash and Ground Granulated Blast Furnace Slag, Respectively, on Mechanical Properties
The compressive strength and splitting tensile strength of the dredged silt blocks were systematically examined using the pressing method, as depicted in
Figure 6 and
Figure 7, incorporating partial replacements of OPC with FA and GGBS. Both FA and GBSS addition can lead to a decrease in the early strength of the block. GBSS reduces the strength of the block at 3 d, and after 28 d, the strength can approach that of OPC. Compared with pure cement test blocks, the addition of 50% GBSS reduces the compressive strength by 37.97% and 8.57% at 3 and 28 d, respectively. The graphical representation of the observed trends indicates a consistent increase in compressive strength across various mixtures as the curing period extends, without indication of a strength reverse shrinkage phenomenon during this progressive period of curing.
The compressive strengths of the blocks without SCMs at 3, 28, and 90 d were 51.5 MPa, 62.2 MPa, and 63.7 MPa, respectively. These data indicate that the majority of strength development for blocks with OPC occurs before the 28-day mark, with only modest gains in strength thereafter. In contrast, FA exhibits lower early reactivity, which leads to a significant reduction in the initial compressive strength. As the FA content increases, there is a noticeable decline in strength, particularly at early stages. For instance, blocks with 50% FA content displayed the lowest early compressive strength at 3 d, recording only 19.1 MPa. This reduction is attributed to FA’s slower hydration reaction, which produces fewer hydration products in the initial stages, resulting in weaker bonding. This is because FA produces fewer hydration products in the early stages, resulting in less compact bonding. While the strength development curve of OPC tends to plateau, the inclusion of FA still yields a significant strength increase after the 28-day mark. FA necessitates an extended curing period to fully manifest its reactivity, accounting for the observed lower early strength. However, as hydration reactions proceed, FA generates more hydration products, filling the slurry structure and improving block strength. The early weakness of FA limits its application in OPC, but its strength continues to increase with a significant growth rate, making it suitable for situations with high demands for later-stage strength. Similarly to FA, GGBS reduces early strength (at 3 d), albeit to a lesser extent compared to an equivalent FA content. At 28 d, the strength of the silt blocks containing GGBS is slightly lower than that of the silt blocks comprising only OPC. There is rapid strength development from 3 d to 28 d, indicating the quick hydration reaction of the GGBS. GGBS exhibits high reactivity, and its hydration degree is high at 28 d, with strength close to OPC when used at 50% content. While GGBS decreases strength at 3 d, it gradually approaches the strength of OPC after 28 d, whereas FA reduces strength at all ages. Compared to FA, GGBS contains not only SiO2 and Al2O3 but also a higher amount of CaO, belonging to the calcium–silicon–aluminum system.
By incorporating FA and GGBS as fine admixtures in the system, a portion of OPC is replaced, leading to the addition of mineral SCMs that fill the small voids between OPC and its hydration products. This results in enhanced compactness of the paste. Furthermore, the introduction of mineral admixtures alters the particle size distribution of the cementitious material system, effectively eliminating existing large-pore voids and promoting a more uniform distribution of pores [
23]. This not only increases the quantity of formed gel but also ensures a more even distribution of hydration products throughout the entire interface transition zone.
3.3. Influence of Different Proportions of Fly Ash and Ground Granulated Blast-Furnace Slag, Respectively, on Dry Shrinkage Performance
The small particle size of dredged silt inherently exacerbates issues related to shrinkage, leading to enhanced water adsorption on the surface of these fine particles. This leads to poor compaction and ineffective reduction in capillary pore water evaporation, resulting in significant drying shrinkage [
18]. Drying shrinkage, a crucial parameter influencing concrete durability, plays a pivotal role in determining the longevity of concrete structures. A smaller drying shrinkage rate corresponds to a reduced degree of volume reduction and diminished formation of microcracks within the concrete matrix. This limited development of microcracks serves to decrease the permeability and permeation parameters of the concrete, ultimately yielding durable concrete materials with enhanced longevity [
24]. Consequently, by reducing the drying shrinkage rate, not only can the overall quality of concrete be enhanced, but its resistance to external factors can also be strengthened, ultimately achieving long-term reliable performance.
Figure 8 shows the drying shrinkage values of dredged silt blocks with different proportions of SCMs. Research results showed that the drying shrinkage curves of dredged silt blocks containing FA and GGBS were essentially the same within the first 10 d, with minimal differences. This indicates that the addition of GGBS and FA can reduce the drying shrinkage of the silt blocks in the later stages. As time progresses, the drying shrinkage of the dredged silt blocks with FA begins to decelerate after 20 d, while the blocks without FA continue to shrink until 40 d before slowing down. The drying shrinkage of the blocks containing FA is lower than that of the blocks without FA. Specifically, at 120 d, the blocks incorporating 20%, 30%, 40%, and 50% FA demonstrated reductions in drying shrinkage values of 12.1%, 16.2%, 27.1%, and 29.7%, respectively. This indicates that a higher FA content exhibits a more pronounced inhibiting effect on drying shrinkage. The primary reason for this behavior is that FA has a slower rate and degree of participation in hydration reactions, thereby slowing down the overall hydration process within the system. This reduction in the rate of water consumption by hydration reactions, combined with the gradual hydration process of FA, acts as a skeletal structure, limiting the shrinkage of the silt blocks. In the early stages, the high elastic modulus of FA particles plays a role in restraining shrinkage. With prolonged time and increased FA content, the effect of restricting drying shrinkage becomes more significant.
The blocks containing 20%, 30%, 40%, and 50% GGBS showed reductions in drying shrinkage values of 8.1%, 14.8%, 21.6%, and 27.1%, respectively, at 120 d. This trend demonstrates that a higher GGBS content enhances the effect on inhibiting drying shrinkage. The main reason is that the addition of GGBS reduces the evaporation of water from the silt blocks under drying conditions. The active components in GGBS react with the hydration products of OPC, forming gel-like substances such as hydrated calcium silicate gel. These gel-like substances have cementitious properties and can fill the microscopic pores within the concrete, reducing the connectivity of the pores. As a result, the loss of moisture and the occurrence of drying shrinkage are reduced.
Furthermore, the addition of GGBS refines the pore structure within the concrete mix, making it more challenging for water to migrate under drying conditions. This is supported by Saluja’s research [
25]; introducing extremely fine GGBS as a substitute for OPC in ordinary concrete containing crushed gravel aggregates has been found to generate a denser concrete matrix. This type of concrete exhibits finer capillary pores, resulting in a reduced availability of free water and consequently creating higher capillary pore water pressure, leading to increased shrinkage strain. Similarly, Shariq et al. [
26] also found that as the substitution level of OPC with GGBS increased, the shrinkage strain also increased. The reason for the difference between this article and their research findings is attributed to the utilization of fine dredged clay particles, significant filling of GGBS in the pores, and a notable enhancement in the particle gradation effect of the system.
3.4. Thermogravimetric Analysis
The chemical composition, pozzolanic reactivity, and particle dimensions of FA and GBSS are dissimilar, culminating in distinct hydration byproducts. The secondary pozzolanic reactions of FA and GGBS deplete the calcium hydroxide (CH) present within the paste, concurrently modifying the quantity and constitution of the resultant hydration byproducts.
Figure 9 presents the differential scanning calorimetry (DSC) and thermal gravity analysis (TG) curves of the hydration products of binary cementitious materials containing 50% FA and GGBS at 28 d. The DSC curve shows the main endothermic peaks of different samples occurring at approximately 90 °C, 430 °C, and 670 °C, which correspond to the decomposition processes of CH and calcium carbonate (CaCO
3). The temperature ranges of these peaks are approximately 40 °C to 220 °C, 420 °C to 470 °C, and 620 °C to 700 °C, respectively. These ranges are indicative of the evaporation of water in varying states within the cementitious matrix, the decomposition of CH, and the disintegration of CaCO
3, respectively.
In the paste, water exists in two states: physically bound water and chemically bound water. These two states cannot be easily distinguished during the evaporation process. To facilitate research, a definition is provided: water that is removed above 105 °C is referred to as non-evaporable water, while water removed below 105 °C is referred to as evaporable water.
The TG curve can be divided into six stages based on different weight loss mechanisms. Stage 1 (40 °C to 105 °C) corresponds to the loss of evaporable water, which refers to the moisture absorbed from the air prior to testing and subsequently dried out from the specimen. This weight loss is primarily influenced by the specific surface area of the binary cementitious paste samples.
Stage 2 (105 °C to 420 °C) corresponds to the loss of non-evaporable water, primarily attributed to the dehydration of the hydrates in the paste. The amount of non-evaporable water lost in the paste of OPC and 50% GGBS is similar and significantly higher than that in the paste containing 50% FA. This indicates that the OPC and 50% GGBS paste have a significantly higher amount of hydrated gel products compared to the paste with FA. Furthermore, FA exhibits the slowest hydration rate, with only a small proportion of FA particles undergoing hydration and minimal gel product formation at the 28-day mark. This analysis provides insights into the principal rationale for the pronounced reduction in block strength during the early phases following the substitution of cement with FA.
The thermogravimetric decomposition of pure calcium hydroxide typically occurs within the temperature range of 500 °C to 800 °C. However, when calcium hydroxide is mixed with other hydrated products and substances, its decomposition temperature may be lower than 500 °C. Consequently, Stage 3 (420 °C to 470 °C) primarily involves the weight loss due to the decomposition of CH in the paste. Compared to OPC, the pozzolanic activity of FA significantly consumes the CH content present in the paste. As the temperature continues to rise beyond 500 °C, the residual CH within the paste undergoes further decomposition, resulting in continuous mass loss throughout this stage.
The weight loss caused by water loss in Stage 4 (470 °C to 620 °C) and Stage 6 (700 °C to 950 °C) is much lower than that in Stage 2. The differences among the three types of pastes are not significant, indicating that the dehydration mechanisms of these pastes are similar at high temperatures.
Stage 5 (620 °C to 700 °C) represents the weight loss due to the decomposition of calcium carbonate (CaCO3) in the paste. Compared to OPC, the weight loss caused by the thermal decomposition of CaCO3 is slightly reduced in the pastes with solely FA or solely GGBS. This reduction is likely related to the decrease in CH content and the improved resistance to carbonation in the paste matrix.
The findings delineated in
Section 3.2 and
Section 3.3 of this manuscript demonstrate that the utilization of FA and GGBS as substitutes for cement reduces the initial strength of silty soil blocks, without negatively impacting their ultimate strength. In comparison to FA, the incorporation of GBSS significantly augments the strength of the blocks. Moreover, the concurrent addition of both GBSS and FA ameliorates the desiccation shrinkage of the blocks. Analysis via TG-DSC above unveils variations in the hydration byproducts within a binary cementitious system inclusive of FA and GBSS, facilitating a comprehensive understanding of the principal causations and mechanisms underpinning these outcomes.
3.5. Pore Structure Analysis
Based on the results shown in
Figure 10, the binary cementitious material system with 50% FA and GGBS undergoes changes in pore size distribution after 28 d of hydration. It can be observed that the addition of different GGBS and FA leads to a reduction in pore size and an increase in the number of small pores, resulting in a finer pore structure of the paste. Compared to FA, GGBS demonstrates a better effect in refining the pore size and shows superior pore refinement.
The specific surface area of OPC given in
Table 1 is 350 m
2/kg, while the specific surface area of FA is 375 m
2/kg; the difference between the two is not significant. Furthermore, as depicted in
Figure 11, the majority of FA particles fall within the size range of 0.01 mm to 0.1 mm, indicating that the particle size distribution of FA is of the same magnitude as OPC cement and incapable of filling the smaller interstitial voids. Additionally, due to the low reactivity of FA, it cannot produce a substantial amount of cementitious material to fill the gaps. Moreover, FA contains a considerable proportion of inert (non-reactive) crystalline phases, and the slow hydration reaction leads to the sedimentation of FA particles and inert crystalline materials within the existing pore structure, potentially increasing the heterogeneity of the pore structure [
27,
28]. In contrast, GGBS has a faster hydration rate and undergoes a more complete secondary pozzolanic reaction by 28 d, producing a significant amount of gel. GGBS refines the critical pore throats, which are the smallest continuous channels within the pore structure. The GGBS also alters the chemical composition and growth pattern of C-S-H, which in turn affects the pore structure. These gels can fill more large pores. The size and connectivity of pores play crucial roles in determining the drying shrinkage of the specimens. Larger pore diameters facilitate quicker moisture loss from the interior of the specimens, which in turn increases drying shrinkage. Conversely, a denser pore structure with limited connectivity restricts the movement of water molecules, potentially beneficial in reducing moisture loss, but can also increase capillary stress within the material. An overly dense pore structure increases capillary stress within the system and may lead to the development of internal cracks, thereby reducing the strength of the material.
3.6. Scanning Electron Microscopy Analysis
Figure 12 presents the SEM images of the hydration of a binary cementitious material system at 28 d. In
Figure 12a, the microstructure of the OPC paste at 28 d reveals the presence of abundant CH crystals. However, the C-S-H gel content is insufficient to fill all the pores, resulting in numerous unhydrated micrometer-scale voids. After adequate hydration reaction, the paste exhibits increased compactness, with hydration products nearly filling all the micrometer-scale voids and no apparent defects.
Figure 12b shows the hydration of a paste containing 50% FA, which appears porous and loosely packed. The image reveals the presence of numerous unhydrated FA particles on the surface, along with well-crystallized CH. The interfaces between C-S-H gel, unhydrated FA, and CH particles are clearly defined. At 28 d of hydration, the crystalline CH phase does not show a significant reduction, and the pozzolanic effect of FA is still limited. There is poor bonding between FA particles and the paste, with a large number of exposed, smooth-surfaced FA spheres and semispherical pits resulting from FA detachment. The hydration products exhibit complete crystallinity, and there are large hexagonal plate-shaped CH particles that are stacked and distributed in layers. It can be observed that the hydration of FA at 28 d is minimal, leading to a decrease in early strength of FA-containing pastes and limiting the effectiveness of FA. However, the hydration degree increases significantly in the later stages, resulting in significant strength development. The morphology effect, pozzolanic activity, and micro-aggregate effect of FA all have an impact on the composition, structure, and properties of cement pastes, particularly favoring the development of later-stage strength. Enhancing the early strength of high-volume FA cement pastes is crucial for promoting the widespread application of FA.
Figure 12c,d are the polished surface and cross-section SEM images, respectively, of the hydration of a binary GGBS–cement system at 28 d. From the polished section SEM image in
Figure 12c, it can be seen that there are still some large GGBS particles (above 10 µm) that have not participated in the reaction. Although the content of finer GGBS particles (below 10 µm) in the paste is relatively small, these particles exhibit higher reactivity. Unhydrated GGBS particles show good bonding with the paste interface. Hydration products such as calcium silicate hydrate (C-S-H) gels fill the large pores, reducing defects in the paste and improving the bonding between different phase interfaces. From the cross-section SEM image in
Figure 12d, it is evident that the GGBS–cement paste exhibits good compactness, and intact crystalline calcium hydroxide (CH) is difficult to identify within the paste. This indicates that a secondary pozzolanic reaction occurred, with GGBS and CH reacting to form C-S-H. The physical filling and pozzolanic effect of GGBS optimize and compact the microstructure of the paste.
4. Conclusions
(1) The molding method plays a pivotal role in the mechanical properties of dredged silt blocks. Compared to conventional vibratory molding, the compaction method significantly improves the compressive and splitting tensile strengths of the specimens. For instance, blocks made from silt with 70% cement and 30% GGBS as cementitious materials achieved compressive and splitting tensile strengths of 64.8 MPa and 5.6 MPa, respectively, after 28 days of curing. These represent improvements of 111.07% and 143.48%, respectively, compared to blocks prepared with the same mix ratio using vibratory molding. The presence of sand particles within the dredged silt provides a skeletal support and better particle matching, which contribute to improving properties of block. The properties of the silt blocks can be significantly enhanced through mechanical force, particle gradation, and hydration action.
(2) The addition of FA and GGBS reduces the early strength of the block to a certain extent but without a significant adverse effect on later strength. At 28 d, the compressive strength of blocks containing 50% FA and GGBS reached 54.0 MPa and 60.8 MPa, respectively. Both GGBS and FA exert notable impacts on reducing drying shrinkage. The dry shrinkage values of dredged soil blocks with 20%, 30%, 40%, and 50% FA and GBSS added at 120 d. were reduced by 12.1%, 16.2%, 27.1%, 29.7%, and 8.1%, 14.8%, 21.6%, and 27.1%, respectively, compared to the dredged blocks without FA. The optimal mix ratio that meets the requirements of blocks such as protective tiles and pavement tiles is that the mass ratio of binder: dredged silt = 1:2.5, OPC: GGBS or FA = 5:5, water-to-binder and silt ratio of 0.15 and semi-dry compression molding with a forming pressure of 15 MPa.
(3) TG-DSC analysis reveals that the quantity of gel formed in OPC and 50% GGBS paste is significantly higher than that in the FA paste, with a notable loss of non-evaporable water. GGBS or FA reacting with CH to form C-S-H significantly consumes the CH present in the paste. MIP analysis indicated that GGBS exhibits superior pore structure refinement compared to FA, which restricts water migration, contributing to reduced drying shrinkage. FA slows down hydration reactions and provides a framework to limit block shrinkage. SEM analysis shows that GGBS–cement paste exhibits good compactness, while FA paste appears porous, loosely packed, and has some unhydrated particles on the surface. Physical filling and the volcanic ash effect of FA and GGBS can optimize and compact the microstructure of paste. Hydration products such as C-S-H gels fill the large pores to reduce defects in the paste and improve the bonding between different phase interfaces.
(4) Utilizing discarded dredged soil as a substitute for conventional sand and gravel materials, and employing large quantities of industrial by-products such as GGBS and FA to replace conventional high-energy-consuming cement, high-strength artificial blocks can be fabricated through compaction molding to replace ordinary concrete. These blocks can be used for the production of revetment bricks, pavement bricks, ballast blocks, etc., and applied in proximity to channel regulation projects, roads, or municipal engineering. The preparation of artificial blocks such as road bricks and ballast blocks using dredged soil as the main raw material has been applied in projects such as the Yangtze River waterway regulation in China and Skikda Port in Algeria. Future tests can be conducted to evaluate the water erosion resistance, chloride ion erosion resistance, and the durability performance against freezing and thawing, carbonation, and permeation of the dredged soil blocks. These tests will lay the groundwork for their comprehensive promotion and application in water-related areas, as well as in cold and coastal regions.