1. Introduction
As is known, today a large share in the field of structural materials is occupied by metal alloys and steels, used in various industries, including in the field of nuclear and alternative energy [
1]. However, in view of the latest global trends in the energy sector, associated with the transition to the creation of power plants operating at high temperatures (approximately 1000–1500 °C, and in some cases approximately 2000 °C), the use of traditional metal alloys is impossible due to their low resistance to high-temperature influences [
2,
3]. The most promising solutions in this direction are composite ceramics that are based on oxide and nitride compounds of aluminum, silicon, zirconium, vanadium, tungsten, and other refractory elements [
4,
5,
6]. The use of such samples makes it possible to increase the reliability of the operation of structural materials operating at ultra-high temperatures, as well as to avoid emergency situations associated with the processes of thermal expansion and oxidation. Also, ceramic materials have recently played an important role in the field of creating alternative types of nuclear fuel, due to the need to change the concept of creating a new generation of nuclear reactors, which is based on the need to increase the temperature of the core, as well as the degree of burnup of nuclear fuel, which excludes the possibility of using traditional metal alloys due to their low thermal stability and corrosion resistance [
7,
8]. In turn, composite ceramics based on oxide and nitride compounds have high inertness to degradation processes, associated with both exposure to aggressive environments and temperature influences, and high strength indicators (hardness, wear resistance, and resistance to cracking and fracture) which allow these ceramics to be used under high mechanical and temperature loads [
9,
10]. Moreover, in contrast to single-component ceramics with sufficiently low strength indicators, the proposed solution related to the creation of composite ceramics, the manufacturing principle of which is based on the combination of phase transformations and morphological features in order to improve their properties, is one of the most promising solutions in the field of creating structural materials.
Interest in composite ceramics based on compounds of aluminum oxide and silicon nitride is manifested not only when considering these materials as structural materials with higher thermal conductivity and mechanical strength, but also the possibility of creating filter elements based on them, with the possibility of changing their morphological features when varying the ratio of components [
11]. The technological process of the synthesis of Al
2O
3–Si
3N
4 ceramics, as a rule, is carried out in a nitrogen atmosphere at elevated temperatures, the main purpose of which is to eliminate the oxidation processes, such as Si
3N
4→ Si
3N
4(SiO
2), as well as to preserve the thermophysical properties of silicon nitride. The oxidation process of Si
3N
4→SiO
2 itself is caused by the thermodynamic instability of silicon nitride, which is accompanied by oxidation processes, and, therefore, changes in its thermophysical, corrosion, and strength parameters [
12].
In one of the first works [
13] devoted to the synthesis of Al
2O
3–Si
3N
4 ceramics, it was shown that the use of a stabilizing additive of magnesium oxide at temperatures above 1200 K leads to the formation of glass phases, which subsequently form aluminum-magnesium spinels, as well as the MgSiO
3 phase, which has an adverse effect on the strength properties of ceramics. At the same time, annealing in a nitrogen atmosphere made it possible to preserve the a-, β-Si
3N
4 phases in the composition of the ceramics. It should also be noted that, in most cases, the synthesis of composite ceramics based on Al
2O
3–Si
3N
4 compounds is limited to the substitution range within 0.1–0.3 M, the result of which is the production of ceramics with a substitution-type structure or with the formation of (SiAl)(ON) solid solution phases, which have fairly good strength and thermal conductivity, although the oxygen vacancies and defective inclusions associated with the manufacturing processes of ceramics play a major role in determining the thermophysical properties of composite ceramics. [
14,
15,
16].
The key aim of this study is to determine the influence of phase composition and dimensional factors on the strength and thermophysical properties of composite ceramics based on xAl2O3–(1−x)Si3N4 compounds, as well as maintaining the stability and resistance of the strength and thermophysical parameters to high-temperature influences, accompanied by oxidation processes in the case of prolonged thermal exposure.
The difference of this study is the thermal sintering of xAl
2O
3–(1−x)Si
3N
4 ceramics by varying the ratio of components in an oxygen-containing environment, eliminating the need for procedures associated with the nitriding or thermal annealing of ceramics in a nitrogen atmosphere, which makes it possible to reduce the cost of ceramic manufacturing technology, as well as to obtain composite ceramics that combine the properties of silicon nitride and aluminum oxide, alongside the transitional phases associated with the phase transformation processes. Interest in composite ceramics based on oxide and nitride compounds is due to the possibility of using them as solid oxide fuel cells [
17], as materials for energy applications (in particular, as structural materials for new generation nuclear fuel [
18,
19,
20,
21,
22]), and also as catalysts [
23,
24,
25,
26,
27].
3. Results and Discussion
The results of the influence of variations in the concentration of the components of the xAl
2O
3–(1−x)Si
3N
4 ceramics on the change in grain size (median size) are presented in the form of diagrams of the grain size distribution in
Figure 1. Furthermore, the results regarding the dependence of the change in median size on the concentration of the components are presented in
Figure 1.
Figure 2 reveals the results of a microstructural analysis of the studied xAl
2O
3–(1−x)Si
3N
4 ceramics, contingent upon the variation in the ratio of components, performed using the scanning electron microscopy method. These images reflect changes in the morphology of the resulting ceramics when the ratio of components changes, on the basis of which we can conclude that when the ratio of components varies, there is a change in both the size of the grains and the density of their agglomeration, which consists in the formation of agglomerates of grains united with each other. It is important to highlight that an elevation in the contribution of the Al
2O
3 phase results in enlargement of the grains, the shape of which is characteristic of the Al
2O
3 phase (in comparison with the initial data for samples of single-component Al
2O
3 ceramics).
Figure 3 reveals the results of an X-ray phase analysis of the studied xAl
2O
3–(1−x)Si
3N
4 ceramics depending on the variation of the components. Descriptions of the results of the morphological features that are associated with changes in the median grain size (see the data in
Figure 1a) as well as of the phase transformations caused by changes in the ratio of components are given together to determine the relationship between morphological features and the phase composition of the ceramics. The presence of two or more phases in the composition of the ceramics, depending on the variation of the components having different grain sizes, as well as the dynamics of changes in their contributions, is clearly visible in the presented grain distribution diagrams. According to the diagrams, variation in the concentration of the components in the composition of the ceramics leads to the displacement of fine grains, the sizes of which are in the order of 0.3–2 microns, followed by their subsequent agglomeration into larger grains with sizes in the order of 5–15 microns.
The observed oxidation processes associated with the formation of the SiO
2 phase, in the case of silicon nitride without the addition of aluminum oxide, is due to the effect of the partial decomposition and subsequent replacement of nitrogen with oxygen in the structure of silicon nitride, which leads to the formation of inclusions in the form of SiO
2. This effect is due to the conditions of thermal annealing in an oxygen-containing environment, which leads to the possibility of introducing oxygen into silicon nitride, with the subsequent formation of an impurity phase SiO
2. When 0.05 M Al
2O
3 is added to silicon nitride, the resulting X-ray diffraction patterns do not reveal the presence of reflections that are characteristic of aluminum oxide phases, and the main alterations are associated with changes in the weight contributions of the previously established tetragonal SiO
2 and hexagonal Si
3N
4 phases, which indicates that the phase transformation processes are associated with the formation of the oxide phase SiO
2. At the same time, the analysis of changes in the median grain size (see data in
Figure 1b) indicates a slight increase in size, which can be explained by the effects of agglomeration during the formation of the SiO
2 phase.
The presence of a local maximum in the presented graph of the median grain size in the ceramics at an Al
2O
3 concentration of 0.1 M may be due to the effect associated with the formation of the hexagonal solid solution phase (SiAl)(ON), the formation of which is observed only at this Al
2O
3 concentration, and with a further increase in concentration, the formation of a stable Al
2O
3 phase with an orthorhombic crystal lattice is observed (according to the X-ray phase analysis data). The very formation of this phase of the solid solution (SiAl)(ON) is due to the partial replacement of the Si–N bonds with Al–O bonds in Si
3N
4 [
28]. It should be noted that the presence of this phase, observed only at low concentrations of Al
2O
3, can be explained by the fact that at a low concentration of aluminum oxide, the formation of a stable Al
2O
3 phase in the composition does not occur, and the phase formation process is accompanied not only by transformations of the Si
3N
4 Si
3N
4/SiO
2 type, but also by the partial replacement of bonds, with the subsequent displacement of inclusions from Si
3N
4 in the form of (SiAl)(ON) grains. In turn, anomalous grain growth may be due to the effects of agglomeration and adhesion due to the presence of a transitional phase (SiAl)(ON). The presence of this phase in the synthesis of Al
2O
3–Si
3N
4 ceramics, in the case of adding a low concentration of nanosized Al
2O
3 particles, was shown in [
29]. At the same time, the authors also identified reflections that were characteristic of the Si
2N
2O phase, the formation of which is associated with thermal exposure at a temperature of 1650 °C in a nitrogen atmosphere.
At an Al
2O
3 concentration of 0.3 M, thermal annealing leads to the formation of the orthorhombic phase Al
2(SiO
4)O, which adheres to the spatial system of Pbnm(62) (PDF-01-074-0274), the formation of which occurs as a result of the interaction of silicon oxide formed as a result of the phase transformation of Si
3N
4 Si
3N
4/SiO
2 with the aluminum oxide phase (PDF-00-046-1212), stable reflections of which are recorded at an Al
2O
3 concentration of 0.2 M and higher. It should be noted that a change in the ratio of the components associated with a rise in the contribution of Al
2O
3 leads to the preservation of the trend of phase transformations of silicon nitride of the Si
3N
4 Si
3N
4/SiO
2 type, and the trend in the content of the silicon oxide phase in the composition decreases slightly, due to the fact that most of this oxide is involved in the formation of the Al
2(SiO
4)O phase. At Al
2O
3 concentrations above 0.7 M, the contribution of the Si
3N
4 phase in the composition of the ceramics, according to the X-ray phase analysis data, is not observed, nor is the contribution of the SiO
2 phase, which indicates that at low concentrations of Si
3N
4 (no more than 0.3 M), thermal annealing leads to a complete transformation of Si
3N
4→ SiO
2, which in turn participates in the formation of the Al
2(SiO
4)O phase. At the same time, a growth in Al
2O
3 concentration above 0.8 M results in coarsening of the grain sizes (see data presented in
Figure 1a,b), which implies the enlargement of agglomerates due to the displacement of the Al
2(SiO
4)O phase and the dominance of the Al
2O
3 phase in the composition of the ceramics.
Based on a comprehensive analysis of the obtained series of X-ray diffraction patterns, changes in the phase composition were determined in the case of varying the ratio of the components in the composition of the xAl
2O
3–(1−x)Si
3N
4 ceramics, the results of which are presented in
Figure 4. The determination of the weight contributions of each phase was carried out by determining the contribution of the areas of diffraction reflections for each established phase on the X-ray diffraction pattern, followed by recalculation of the contributions, considering the corundum numbers taken from the PDF-2 database. According to the presented diagram, it is possible to determine the main phase changes associated with the processes of phase formation with a variation in the ratio of the components in the composition of the ceramics, as well as to establish the phase transformation dynamics in the ceramics, the general form of which can be presented as follows (1):
Table A1 in
Appendix B shows the crystal lattice parameters for all of the established phases depending on the concentration of the components in the ceramic composition, reflecting changes in the structural parameters associated with phase formation processes.
Figure 5a,b illustrates the assessment results of the changes in material density and porosity, calculated based on data comparing the density of samples obtained by measurements using the Archimedes method and theoretical values of the density of samples. As is evident from the presented dependences of the change in density, the formation of the Al
2(SiO
4)O and Al
2O
3 phases with a change in Al
2O
3 concentrations leads to only small changes in the density of the ceramics from 3.3 to 3.45 g/cm
3, which are caused by a change in the ratio of the phases in the composition. In this case, an increase in the contribution of the Al
2O
3 phase results in an increase in the ceramic density, which is due to a higher density of Al
2O
3 (ρ
Al2O3 = 3.98 g/cm
3).
Figure 5b shows the results of a comparative analysis of the change in the density of the studied samples, obtained using the Archimedes method with the calculated data obtained on the basis of the structural analysis data. As can be seen from the presented data, changes in the phase composition lead to a decrease in the difference in density values, which allows us to judge the convergence of the density results that were obtained using the Archimedes method and the structural analysis data.
Figure 6 demonstrates the results of Raman spectroscopy of the studied xAl
2O
3–(1−x)Si
3N
4 ceramics depending on the variation in the concentration of the components, which reflect the change in the fundamental modes associated with the formation of phases and their structural ordering. The spectra of Si
3N
4 without the addition of Al
2O
3 contain peaks at 253, 357, and 497 cm
−1, which may belong to the α-Si
3N
4 phase. Peaks at 253 and 497 cm
−1 correspond to the A
1g modes, and a peak at 357 cm
−1 corresponds to the E
g mode [
30]. In addition, low-intensity peaks at 178, 196, and 224 cm
−1 can be associated with the β-Si
3N
4 phase [
31]. The peak in the region of 800 cm
−1 is characteristic of the SiO
2 phase, the formation of which occurs as a result of the oxidation process under the thermal influence associated with the processes of replacing nitrogen with oxygen, with the subsequent formation of inclusions in the form of SiO
2 [
32]. At Al
2O
3 concentrations in the x range from 0.05 M to 0.50 M, the spectra change only slightly; small fluctuations in peak intensity are observed only in the region of 650–950 cm
−1. When the Al
2O
3 concentration reaches x = 0.55, peaks appear at 800 and 880 cm
−1, which can be associated with the Al
4+2xSi
2−2xO
10−x phase, the weight contribution of which increased, according to X-ray phase analysis. At a concentration of x = 0.70 M, fluorescence begins to appear in the region of 1200–1800 cm
−1, which may be due to the high corundum content in the samples. At Al
2O
3 concentration x = 0.90 M, a peak appears at 412 cm
−1 corresponding to the A
1g mode of the α-Al
2O
3 phase [
33].
Thus, analyzing the data from the X-ray phase analysis and Raman spectroscopy, it can be concluded that the observed changes are in good agreement with each other, and that both methods together make it possible to determine with sufficiently high accuracy the dynamics of phase transformations in the ceramic samples, depending on the variation in the ratio of the components in the composition.
Figure 7 illustrates the results of hardness measurements of the studied xAl
2O
3–(1−x)Si
3N
4 ceramics in the case of a change in the ratio of components, and as a consequence, variations in the phase composition of the ceramics. The general view of the presented dependence of the change in hardness of the xAl
2O
3–(1−x)Si
3N
4 ceramics with variation in the ratio of the components has a clear dependence on both the phase transformations that occur in the ceramics and the phase content, the change in which causes the hardening effect in comparison with the hardness data for Si
3N
4. The observed changes in hardness at Al
2O
3 concentrations equal to 0.05–0.1 M are due to small changes in the Si
3N
4/SiO
2 phase ratio, the alteration of which occurs as a result of the thermal decomposition processes of Si
3N
4 Si
3N
4/SiO
2. At the same time, the most significant changes in hardness are observed during the formation of the Al
2(SiO
4)O phase in the ceramics, an increase in the contribution of which leads to the strengthening of the ceramics by more than 1.4 times compared to the hardness data for the Si
3N
4 samples. At the same time, the obtained hardness values for the xAl
2O
3–(1−x)Si
3N
4 ceramics at Al
2O
3 concentrations above 0.4 M are in good agreement with the literature data from [
28,
29,
30], in which hardening is caused by both the dimensional factors that are associated with the presence of fine or nanosized grains and with the phase transformations that are caused by changes in the phase ratio in the composition of the ceramics. Displacement of the Al
2(SiO
4)O phase at low concentrations of Si
3N
4 in the ceramic composition leads to a decrease in hardness, which is due to lower hardness values for the Al
2O
3 phase, which is dominant in the ceramic composition.
Figure 8a reveals the results of the measurements of the thermal conductivity of the xAl
2O
3–(1−x)Si
3N
4 ceramics under study, depending on the variation in the ratio of the components in the composition. To compare the results of the changes in the thermal conductivity coefficient, we selected works in which the thermophysical parameters of similar ceramics that were obtained using the methods of mechanical mixing and thermal annealing were studied [
31,
32,
33,
34,
35,
36,
37].
As is known, polycrystalline Si
3N
4 ceramics obtained by hot pressing under high pressure, which eliminates the processes of oxidation and the formation of oxide inclusions in the composition, as well as oxygen vacancies, have fairly good thermal conductivity, which in turn leads to a pronounced dependence on the concentration of defects and oxygen vacancies in the composition [
34]. In this case, thermal annealing of mechanically deformed Si
3N
4 powders, accompanied by the decomposition of the Si
3N
4 → SiO
2 type, leads to the presence of oxygen and silicon vacancies, the formation of which occur according to the mechanism of maintaining electrical neutrality when oxygen replaces nitrogen atoms, with the subsequent formation of vacancies in the silicon sublattice (2O
2 → 4O
*N + V
Si””) [
35]. As a result, the value of the thermal conductivity coefficient for the Si
3N
4 ceramics is about 1.76 W/(m × K). At the same time, comparing the results of changes in thermal conductivity for Si
3N
4 ceramics from this work and work [
32], it can be concluded that thermal annealing of the samples at a temperature of 1500 °C, in comparison with conventional stirring and pressing, makes it possible to more than triple the thermal conductivity of the ceramics by reducing deformation distortions, which are observed as scattering centers and vacancies. The addition of low Al
2O
3 content ceramics to the Si
3N
4 composition (at concentrations from 0.05 to 0.15 M) does not lead to significant changes in the thermal conductivity coefficient (∆TC~2–6%), which indicates that the absence of any significant changes in the phase composition associated with the formation of replacement phases does not have a significant effect on changes in the thermophysical parameters. The most significant changes in thermal conductivity occur at Al
2O
3 concentrations above 0.15 M, which are characterized by the formation of the Al
2(SiO
4)O phase, the appearance of which in the composition of ceramics leads to an increase in the thermal conductivity coefficient from 1.76–1.79 W/(m × K) to 2.56–2.78 W/(m × K), which is more than a 1.5-fold increase in thermal conductivity. At the same time, a trend of increasing thermal conductivity, depending on the variation in the concentration of the components in the ceramic composition, is observed up to Al
2O
3 concentrations equal to 0.6–0.65 M, for which, according to the X-ray phase analysis, the presence of inclusions in the form of silicon nitride in the composition is observed. This growth in thermal conductivity can be explained by several factors. Firstly, according to the X-ray phase analysis data, a change in the phase composition through the formation of the Al
2(SiO
4)O phase results in a porosity decrease, associated both with a change in the density of the ceramics and with size effects caused by the packing density of the grains in the ceramic composition. Secondly, the stabilization of structural parameters due to phase formation processes reduces the concentration of defective inclusions in the composition of the ceramics and also contributes to a change in the number of vacancies, which in turn provides a smaller number of scattering centers that impede heat transfer.
In the case of the concentration of silicon nitride in the composition of xAl
2O
3–(1−x)Si
3N
4 ceramics being less than 0.35 M, according to the X-ray phase analysis data, the Al
2O
3 phase begins to dominate in the composition, which in turn leads to an increase in porosity (according to the porosity measurements taken using the Archimedes method), as well as an enlargement of grain sizes. It should be noted that the observed changes in thermal conductivity in the case of low Al
2O
3 concentrations are in good agreement with the results of other works, while the proposed method for producing ceramics, which eliminates a large number of technological operations, makes it possible to obtain ceramics with fairly high thermal conductivity in comparison with other oxide ceramics, such as ZrO
2 (0.3–3.2 W/(m × K) depending on density and porosity [
36]) and ZrO
2–Al
2O
3 (approximately 2.5–4.5 W/(m × K) depending on the ratio of components [
37]). Moreover, in a number of works [
33,
38,
39], it was shown that the thermal conductivity of ceramics has a direct dependence not only on the concentration of vacancies and defects in the composition but also on porosity. In the case of high porosity, the observed reduction in thermal conductivity is due to a large number of voids, which interferes with the mechanisms of phonon heat transfer and reduces the rate of heat transfer. Direct confirmation of this is the presented comparative analysis of the porosity values and the efficiency of changing the thermal conductivity coefficient, presented in
Figure 8b.
An important factor determining the prospects for using composite heat-resistant ceramics is the assessment of their resistance to high-temperature influences and thermal shocks, as well as maintaining the stability of the strength properties of the ceramics to such influences. For example, in [
40], it was shown that thermal heating leads to a decrease in fracture resistance by more than 400 °C, and the main effect causing such a strong decrease in strength properties is due to the ratio of cations/anions in the composition of the ceramics, the presence of which are associated with the phase composition causing changes in the coefficient of thermal expansion.
Figure 9 illustrates the results of the measurements of the hardness of the ceramic samples, depending on the variation of the components in the composition, obtained during life tests to determine the stability of the strength parameters to long-term thermal effects and the associated oxidation processes. The general trend of the changes in hardness at a test temperature of 700 °C indicates a fairly high resistance of the ceramics to long-term thermal effects, especially for the ceramics that were obtained with an Al
2O
3 content of 0.3–0.6 M. The least stable ceramics were the single-component ceramics, which in turn confirms the applicability of the concept of creating composite ceramics that have higher resistance to external influences compared to single-component ceramics. At a test temperature of 1000 °C, the decrease in hardness during life tests became more pronounced, which in turn may be due to more intense oxidation processes of silicon nitride at high temperatures. A change in hardness, indicating softening and a decrease in resistance to mechanical external influences, in the case of a test temperature of 1000 °C is observed after 400–500 h of successive thermal exposure, which also confirms the fact that with the increase in exposure temperature, the degradation rate of strength properties increases and becomes more pronounced with prolonged exposure.
Figure 10 demonstrates the results of a comparative analysis of the degradation of hardness values as a result of thermal tests associated with oxidation processes. The hardness degradation was determined by comparing hardness values before and after heat resistance tests (after 1000 h) with the subsequent calculation of deviations from the initial value considering measurement error.
As can be seen from the data presented, the formation of the Al2(SiO4)O phase in the composition of the ceramics with a subsequent increase in its content and a decrease in the weight contribution of the Si3N4 phase due to phase transformations leads to a growth in resistance to softening by more than 4–7 times in comparison with the softening data that was established for the single-component ceramics. Such obvious differences in the change in hardness may be associated with the processes of the high-temperature oxidation of silicon nitride, which lead to softening of the ceramics due to a rise in the SiO2 phase, as well as its structural disorder.
The degradation kinetics of the ceramics, contingent upon the temperature of life tests, were determined by the assessment of the phase composition of the ceramics before and after thermal exposure for 1000 h at different temperatures. The results are presented in the form of diagrams in
Figure 11, reflecting the change in the phase ratio associated with oxidation processes.
According to the data obtained, the most significant changes in the phase composition are observed for the ceramics that were subjected to thermal action at a temperature of 1000 °C and are associated with an increase in the contribution of the SiO2 phase. The growth in SiO2 content that was observed for the high-temperature tests is due to the oxidation processes of the Si3N4 phase, which is most pronounced at low contents of the Al2O3 phase, and less pronounced (the change is no more than 1.0–1.5%) for samples in which the formation of the Al2(SiO4)O phase, which has higher resistance to high-temperature corrosion compared to silicon nitride, which is oxidized under the influence of temperature by replacing nitrogen with oxygen with the subsequent formation of silicon dioxide, was observed. Thus, by analyzing the phase changes in the ceramics as a result of thermal effects, we can conclude that the presence of two or more phases in the composition of the ceramics leads to an increase in the stability of the ceramics to oxidation, in particular, a slowdown in the oxidation process of silicon nitride, as well as the maintenance of the stability of the Al2(SiO4)O phase in the case of low silicon nitride contents in the composition of the initial mixture. At the same time, the limiting factor to oxidation and the subsequent degradation of strength properties (reduction of hardness) is the presence of the Al2(SiO4)O phase in the composition of the ceramics, the presence of which also determines higher strength and thermal conductivity. Maintaining the oxidation stability of the composite ceramics at high temperatures, in turn, can be explained by them having higher thermal conductivity, which ensures uniform heat distribution and transfer during prolonged temperature exposure.