3. Results
In this section, mixture compositions for the production of hyperpressed bricks were developed by preparing mixtures with different proportions of marbleized limestone processing waste (MLPW) and white Portland cement (M500). The specimens were manufactured by high-pressure compaction under a pressing load of 200 kN (corresponding to a compaction pressure of 28 MPa). The water-to-cement ratio (w/c) was maintained constant at 0.25 for all mixtures.
Table 1 presents the mixture compositions and the results of the physical and mechanical properties of the specimens after 7 days of curing under moist conditions.
Figure 3 shows photographs of the hyperpressed brick specimens.
As can be seen from
Table 1, the compressive strength values of the specimens are relatively high and correspond to brick grades M350 and M400. When considered as concrete specimens, they correspond to concrete strength classes B25, B27.5, and B30.
An increase in the content of marbleized limestone processing waste (MLPW) in the mixtures, and consequently a decrease in the cement content, resulted in a reduction in compressive strength from 43.1 MPa to 34.1 MPa, while the average density increased from 2108.1 kg/m³ to 2145.1 kg/m³ (Fig. 5). The latter is associated with the higher bulk density of the marbleized limestone processing waste (MLPW) compared with that of cement.
The specimens corresponding to Compositions 2 and 3 exhibited the most favorable strength characteristics. In addition, the MLPW content in these mixtures, excluding the amount of water, was 79–83 wt.%. The compressive strength of these specimens corresponded to brick grades M400 and M350, respectively.
Figure 4.
Average density and compressive strength of the specimens produced with gray Portland cement and molded under a compaction load of 200 kN.
Figure 4.
Average density and compressive strength of the specimens produced with gray Portland cement and molded under a compaction load of 200 kN.
Figure 5 shows the microstructure of a hyperpressed brick specimen manufactured by compaction under a pressing load of 200 kN and fractured during the compressive strength test.
Figure 5.
SEM micrographs of the microstructure of the hyperpressed brick specimen (Composition 2) manufactured by compaction under a pressing load of 200 kN.
Figure 5.
SEM micrographs of the microstructure of the hyperpressed brick specimen (Composition 2) manufactured by compaction under a pressing load of 200 kN.
The SEM image at low magnification (a) (×50, scale bar: 500 μm) shows the overall microstructure of the fractured hyperpressed brick specimen manufactured under a compaction load of 200 kN. The matrix consists of a dense cement stone uniformly surrounding the particles of the marbleized limestone processing waste (MLPW). Despite the high degree of compaction, large and small intergranular pores are observed in several areas (Fig. 5a, b). Their formation is associated with the local incomplete packing of aggregate particles and the non-uniform distribution of cement hydration products. The surface of the large MLPW particles exhibits the characteristic layered fracture morphology of calcite. No cracks typical of materials subjected to compressive failure are observed in the specimen. Overall, the microstructure is highly compact, which is attributed to the intensive compaction pressure providing close contact between the components of the composite.
The SEM image (b) (×200, scale bar: 100 μm) clearly reveals a coarse aggregate particle with a relatively smooth surface, which is typical of carbonate rocks after mechanical fracture. The aggregate surface is almost completely covered by cement hydration products, indicating good bonding between the aggregate and the cementitious matrix. A dense layer of hardened cement paste has formed in the immediate vicinity of the aggregate particle. No visible gaps or signs of debonding are observed at the aggregate–matrix interface, indicating strong interfacial adhesion achieved as a result of the high compaction pressure.
Figure 5c (×2300, scale bar: 10 μm) shows the detailed microstructure of the cement matrix. The high-magnification SEM image reveals a dense cement stone structure composed predominantly of calcium silicate hydrate (C–S–H) gel. The C–S–H phase is uniformly distributed throughout the matrix and interconnects the individual hydration products. Small intergranular spaces remain between the hydration products owing to the incomplete filling of micropores by the hydrated phases. Overall, the microstructure is dense and homogeneous. The hardened calcium silicate hydrate crystals completely bind the aggregate particles into a continuous monolithic structure, which accounts for the high compressive strength of the hyperpressed brick specimen.
Figure 5d (×2700, scale bar: 5 μm) illustrates the hydration products of the white Portland cement. At higher magnification, the principal cement hydration products are clearly distinguishable. The dominant phase is the amorphous gel-like calcium silicate hydrate (C–S–H), which forms a dense three-dimensional network surrounding the aggregate particles. In addition, a relatively small amount of plate-like portlandite (Ca(OH)₂) crystals, a typical product of free CaO hydration, is observed. The C–S–H gel fills the intergranular spaces and binds the individual portlandite crystals into a continuous monolithic structure, indicating the predominance of a fine-dispersed calcium silicate hydrate network that contributes to the high strength of the material.
In this section, the preparation of the molding mixtures and the proportions of the raw materials were identical to those used for the mixtures described in Section 3.1. The specimens were molded at a constant water-to-cement ratio (w/c) of 0.25 and a compaction load of 300 kN.
Table 2 presents the mixture compositions and the results of the determination of the physical and mechanical properties of the specimens after 7 days of curing under moist conditions.
Figure 6 shows photographs of the hyperpressed brick specimens manufactured by compaction under a 300 kN pressing load.
As can be seen from the data presented in
Table 2 and
Figure 7, increasing the compaction load from 200 kN to 300 kN resulted in a slight increase in the average density and a significant improvement in the compressive strength of the specimens. Specifically, the average density increased by 43.3–61.5 kg/m³ (an increase of 2.02–2.90%) compared with the specimens manufactured under a compaction load of 200 kN.
The average density of the specimens of all compositions exceeded 2100 kg/m³, which makes it possible to classify the obtained products as heavyweight concrete according to [
21].
Compared with the specimens manufactured under a compaction load of 200 kN, the compressive strength increased by 1.6–12.2 MPa, corresponding to an increase of 4.7–28.7%. Only a slight increase in strength was observed for Composition 4. In our opinion, this is associated with the low content of binder in the mixture of this composition.
As noted previously, Compositions 2 and 3 exhibited the most favorable strength characteristics. The MLPW content in these mixtures, excluding the water content, was 75–80 wt.%, and their compressive strength corresponded to brick grades M550 and M400, respectively.
Figure 8 shows the microstructure of a hyperpressed brick specimen manufactured under a compaction load of 300 kN and fractured during the compressive strength test.
The SEM image (a) at low magnification (×45, scale bar: 500 μm) shows the overall microstructure of the fractured hyperpressed brick specimen manufactured under a compaction load of 300 kN. The marble aggregate particles exhibit relatively smooth surfaces and are densely surrounded by cement hydration products. The interfacial transition zone (ITZ) between the aggregate and the cement matrix is weakly pronounced, indicating good mechanical bonding between the components. The specimen is characterized by fracture cracks formed during the compressive strength test. The hydration products almost completely fill the space between the aggregate particles, forming a dense and continuous cementitious matrix. The absence of large pores confirms the high degree of densification achieved under the 300 kN compaction load.
Image (b) (×70, scale bar: 200 μm) shows the interface between a coarse marble aggregate particle and the surrounding cement matrix. The aggregate surface is characterized by a relatively smooth texture resulting from the calcitic nature of the rock. Despite the comparatively low surface roughness of the aggregate, the cement hydration products exhibit good adhesion to its surface, as the applied compressive load did not disrupt the integrity of the interfacial transition zone (ITZ). Furthermore, this indicates that the effective bond was achieved not only through adhesion but also as a result of the high compaction pressure applied during the hyperpressing process. Narrow fracture cracks are observed within the cement matrix, having formed during the compressive strength test of the specimen.
At higher magnification,
Figure 8c (×1000, scale bar: 10 μm) more clearly reveals the microstructure of the interfacial transition zone (ITZ) between the surface of the marbleized limestone processing waste (MLPW) aggregate and the cement stone. The surface of the MLPW particles is covered with a dense layer of hydration products, predominantly consisting of fibrous and gel-like calcium silicate hydrate (C–S–H). The interfacial transition zone exhibits a high degree of integration without pronounced voids, indicating strong mechanical bonding between the aggregate and the cement matrix. A localized microcrack is observed within the cement stone, most likely formed as a result of shrinkage stresses during drying or during specimen preparation for SEM analysis. This crack does not propagate along the phase boundary, indicating the high strength of the contact zone between the aggregate and the cement matrix.
The high-magnification SEM image (d) (×3500, scale bar: 5 μm) illustrates the morphology of the hydration products of white Portland cement (M500). The cement matrix is predominantly composed of amorphous calcium silicate hydrate (C–S–H) gel, which forms a dense three-dimensional network between the hydration products. In addition, plate-like crystals of calcium hydroxide (Ca(OH)₂), characteristic of Portland cement hydration, are observed. Small intergranular spaces remain between the individual hydration products; however, their limited size indicates a high degree of structural densification. The uniform distribution of calcium silicate hydrate (C–S–H) throughout the matrix, on the aggregate surfaces, and within the intergranular spaces produces a dense microstructure and contributes to the high compressive strength of the hyperpressed brick specimen.
Thus, mixture compositions for the production of hyperpressed bricks were developed, and the properties and microstructure of the resulting specimens were investigated. Manufacturing the specimens under a compaction load of 200 kN produced compressive strengths ranging from 34.1 to 43.1 MPa, corresponding to concrete strength classes B25–B30. Increasing the compaction load to 300 kN resulted in compressive strengths of 39.7–51.6 MPa, corresponding to concrete strength classes B27.5–B40. The specimens containing 75–80 wt.% marbleized limestone processing waste (MLPW) exhibited the most favorable performance characteristics (
Table 3 and Table 4). Microstructural analysis showed that compaction under higher pressure produced specimens with a denser microstructure and a stronger contact zone between the aggregate particles and the cement matrix. Consequently, the manufactured products satisfied the performance requirements for hyperpressed bricks.
The results of this study demonstrate that the production of high-strength hyperpressed products incorporating marbleized limestone processing waste (MLPW) is governed by two principal factors. The first and most important factor is the compaction pressure, which should be at least 300 kN. The second factor is the cement grade, which should be not lower than M450. Under such a high compaction load, the mineral aggregate particles and the cement binder are forced into close contact, effectively filling the voids between them. At the same time, intensive internal friction and interparticle contact are generated, promoting strong bonding between the particles at both the molecular and crystalline levels.
In this section, the properties of hyperpressed brick specimens produced using gray Portland cement (M450) were investigated. To ensure comparable experimental conditions and results, the same mixture compositions previously used for the specimens produced with white Portland cement were adopted (Table 5). As demonstrated by the experimental results, the highest performance of the specimens produced with white cement was achieved at a compaction load of 300 kN. Therefore, the same compaction load was used for manufacturing the specimens with gray Portland cement.
Table 3 presents the mixture compositions and the results of the physical and mechanical properties of the specimens after 7 days of curing under moist conditions.
Figure 9.
Hyperpressed brick specimens produced with gray Portland cement and molded under a compaction load of 300 kN.
Figure 9.
Hyperpressed brick specimens produced with gray Portland cement and molded under a compaction load of 300 kN.
Figure 10.
Average density and compressive strength of the specimens produced with gray Portland cement and molded under a compaction load of 300 kN.
Figure 10.
Average density and compressive strength of the specimens produced with gray Portland cement and molded under a compaction load of 300 kN.
The experimental results presented in Table 6 show that, after 7 days of curing, the specimens achieved compressive strengths corresponding to brick grades M450 and M400, which also represent high strength levels for hyperpressed bricks. The strength characteristics are slightly lower than those of the specimens produced with white Portland cement, which can be attributed to the higher strength grade of the latter. The increase in average density and the decrease in compressive strength follow the same trends as those observed for the specimens produced with white Portland cement.
Figure 11 shows the microstructure of a hyperpressed brick specimen produced with gray Portland cement, manufactured under a compaction load of 300 kN, and fractured during the compressive strength test.
The SEM image (a) (×110, scale bar: 100 μm) shows the contact interface between the surface of the marbleized limestone processing waste (MLPW) aggregate and the cement matrix. The surface of the MLPW particles is covered with cement hydration products, forming a continuous layer around the aggregate. A microcrack is observed within the cement stone, propagating predominantly through the cement matrix rather than along the phase boundary. This indicates that the adhesion between the aggregate and the cement matrix remains satisfactory, whereas the crack is most likely associated with shrinkage deformation or localized stress concentrations generated during the compressive failure of the specimen.
Image (b) (×500, scale bar: 50 μm) illustrates the interfacial transition zone (ITZ) between the marble aggregate and the cement matrix. The MLPW particles are almost completely encapsulated by cement hydration products, forming a continuous three-dimensional structure. The cement matrix exhibits a dense, fine-grained morphology with a minimal amount of open porosity. The hydration products are uniformly distr ibuted around the aggregate surface, providing strong bonding between the two phases. Virtually no evidence of significant debonding between the cement matrix and the aggregate or the development of microcracks is observed, indicating the beneficial effect of the 300 kN compaction load on the formation of a dense microstructure in the hyperpressed brick specimen.
The high-magnification image (c) (×1500, scale bar: 10 μm) reveals the microstructure of the cement matrix. The matrix is predominantly composed of gel-like calcium silicate hydrate (C–S–H), which forms a three-dimensional network interconnecting the individual particles of the material. In addition to C–S–H, plate-like crystals of calcium hydroxide (Ca(OH)₂), characteristic hydration products of Portland cement, are observed. In several localized regions, needle-like crystalline formations are also present, which may be attributed to ettringite, formed during the early stages of cement hydration and retained within the hardened cement matrix. Small pores remain between the hydration products, indicating a slightly less compact cement matrix than that observed in the specimens manufactured under higher compaction pressure.
The high-magnification image (d) (×3000, scale bar: 5 μm) shows the microstructure of the cement hydration products. The cement matrix is predominantly composed of a dense amorphous calcium silicate hydrate (C–S–H) gel, which surrounds the marble aggregate particles. In addition to the C–S–H gel, isolated plate-like hydrated crystals are uniformly distributed throughout the cement matrix. This combination of amorphous gel and plate-like crystalline hydrates contributes to structural densification and reduces capillary porosity. No large voids are observed between the hydration products, indicating a high degree of cement hydration and effective densification of the material.