Closed Die Upsetting of Aluminum Matrix Composites Reinforced with Molybdenum Disulfide Nanocrystals and Multilayer Graphene, Implemented using the SPS Process—Microstructure Evolution

New methods for producing composite materials such as SPS (Spark Plasma Sintering) are becoming more and more popular due to the ease of implementation in industrial conditions and the versatility of the materials used for processing. In order to fully exploit the potential of this method, modifications were proposed which consisted in the deliberate induction of deformation during the sintering process. The influence of the manufacturing method on the microstructure of aluminum alloy matrix composites reinforced with layered crystals in the form of nanoflakes was investigated. Composites with the addition of 10 vol % of multilayer graphene and molybdenum disulfide were prepared and their density, hardness, and the influence of the deformation ratio on the changes occurring in the microstructure were examined. The potential of the method to shape the properties of the tested composites and the strong dependence of the obtained results on the morphology of the reinforcing phase was indicated. An interesting phenomenon observed for composites with the addition of MoS2 during the process was the reaction of the components leading to in situ formation of the Al12Mo intermetallic phase.


Introduction
A permanent interest in composite materials and the development of a unique group of new materials called two-dimensional (2D) crystals have contributed to an increase in the research and application potential of composites with the addition of those prospective structures. Graphene as the monolayer of carbon atoms-a notorious 2D material-gains a number of interesting properties and a very important application of this material is found in electronics [1]. Its use as a volume component of the composite, although in theory could lead to a significant improvement of properties, in practice is economically unjustified and difficult to implement. Multilayer graphene (MLG) is becoming an increasingly popular form of graphene, which is used to improve the composite's properties [2]. It is easier to obtain and therefore cheaper. Very thin forms of platelets containing several to dozens of layers can also be made for other layered crystals such as MoS 2 and WS 2 [3]. Contemporary research work suggests that the use of nanocrystals in a form similar to a monolayer, as in the case of MLG, proves to be beneficial in view of the possibility of improving the mechanical properties [4][5][6][7]. More often, in addition to structural composites, functional materials are also produced in which nanocrystals similar to 2D structures can improve their thermal [8][9][10], electrical [11], or electromagnetic [12] properties.

Materials and Methods
Two groups of composites based on alloy AA6061 were prepared, firstly with the addition of MLG flakes and secondly with the addition of molybdenum disulfide. In order to obtain the reference material, aluminum sinters without the addition of layered crystals were also made. In each case, aluminum powder AA6061 from the Aluminum Powder Company Ltd. (Minwotrth, UK), Alpoco with the chemical composition shown in Table 1 was used as the matrix material. Larger particles of AA6061 aluminum alloy powder are mostly characterized by an elongated shape and the finer fraction of powder has a spherical shape (Figure 1a). Single large particles with an equivalent diameter exceeding 15 µm can be observed. The mean elongation (α) parameter for the statistical powder particles is 1.3. The MoS 2 nanopowders from Nanostructured and Amorphous Materials, Inc. (Los Alamos, NM, USA) and the multilayer grapheme (MLG powder) trademark "Gn(12)" from Graphene Supermarket were used. In both cases the volume addition of the second phase was 10%. The morphology of the materials used is shown in Figures 1 and 2.
The MLG flakes designation Gn (12) refers to the average thickness of the plates, which according to the producers is 12 nm,. Therefore, one flake comes from an average of about 40 carbon monolayers. The average lateral size of the plates is approximately 4.55 µm (1.5-10 µm). As can be seen from the data presented (Figure 2a), MLG flakes are characterized by a lateral size that is approximately 10 times larger than that of MoS 2 flakes. One can therefore expect a significant difference in their placement already at the stage of the homogenization process. MoS 2 crystals have a similar flake morphology ( Figure 2b). They are characterized by an average lateral dimension of 480 nm and a thickness in the range of 20-40 nm.
Materials 2018, 11, x FOR PEER REVIEW 3 of 18 Considering the facts presented earlier, we decided to discuss the changes in microstructure and basic mechanical properties observed after the modified SPS consolidation processes of AA6061 alloy composites with the participation of MLG and MoS2 layered crystals.

Materials and Methods
Two groups of composites based on alloy AA6061 were prepared, firstly with the addition of MLG flakes and secondly with the addition of molybdenum disulfide. In order to obtain the reference material, aluminum sinters without the addition of layered crystals were also made. In each case, aluminum powder AA6061 from the Aluminum Powder Company Ltd. (Minwotrth, UK), Alpoco with the chemical composition shown in Table 1 was used as the matrix material. Larger particles of AA6061 aluminum alloy powder are mostly characterized by an elongated shape and the finer fraction of powder has a spherical shape (Figure 1a). Single large particles with an equivalent diameter exceeding 15 μm can be observed. The mean elongation (α) parameter for the statistical powder particles is 1.3. The MoS2 nanopowders from Nanostructured and Amorphous Materials, Inc. (Los Alamos, NM, USA) and the multilayer grapheme (MLG powder) trademark "Gn(12)" from Graphene Supermarket were used. In both cases the volume addition of the second phase was 10%. The morphology of the materials used is shown in Figures 1 and 2.  The MLG flakes designation Gn (12) refers to the average thickness of the plates, which according to the producers is 12 nm,. Therefore, one flake comes from an average of about 40 carbon monolayers. The average lateral size of the plates is approximately 4.55 μm (1.5-10 μm). As can be seen from the data presented (Figure 2a), MLG flakes are characterized by a lateral size that is approximately 10 times larger than that of MoS2 flakes. One can therefore expect a significant difference in their placement already at the stage of the homogenization process. MoS2 crystals have a similar flake morphology (Figure 2b). They are characterized by an average lateral dimension of 480 nm and a thickness in the range of 20-40 nm.
After weighing, the powders were mixed in a rotary, horizontal mill in the presence of zirconium balls. The mass ratio of balls to powder was 3:1. The process was carried out with isopropyl alcohol for 8 h. The rotational speed was set at 300 rpm, enabling the smallest number of defects to be introduced into the layered crystals. Previous research [28] has shown that during mixing defoliation the formation of much thinner flakes can occur. At the same time, as shown in the Figure 3, bigger aluminum particles experience small deformations (flattening) due to collisions with ZrO2 balls, making a shape similar to a disk. No significant differences were found in the morphology of aluminum particles after the milling process in the presence of various additives. The mixed suspensions were dried and granulated on 0.3 mm mesh screens. The final stage was the powder consolidation, which ran directly in the SPS device (HP D 10, FCT Systeme GmbH, Rauenstein, Germany), realizing a different strain. The process conditions are presented in Table 2. The first option included a classic, one-step process of SPS consolidation in a graphite matrix with a diameter of 20 mm, temperature T = 550 °C, and pressure of 50 MPa. This process was previously optimized to obtain material of the highest density. After weighing, the powders were mixed in a rotary, horizontal mill in the presence of zirconium balls. The mass ratio of balls to powder was 3:1. The process was carried out with isopropyl alcohol for 8 h. The rotational speed was set at 300 rpm, enabling the smallest number of defects to be introduced into the layered crystals. Previous research [28] has shown that during mixing defoliation the formation of much thinner flakes can occur. At the same time, as shown in the Figure 3, bigger aluminum particles experience small deformations (flattening) due to collisions with ZrO 2 balls, making a shape similar to a disk. No significant differences were found in the morphology of aluminum particles after the milling process in the presence of various additives. The mixed suspensions were dried and granulated on 0.3 mm mesh screens. The MLG flakes designation Gn (12) refers to the average thickness of the plates, which according to the producers is 12 nm,. Therefore, one flake comes from an average of about 40 carbon monolayers. The average lateral size of the plates is approximately 4.55 μm (1.5-10 μm). As can be seen from the data presented (Figure 2a), MLG flakes are characterized by a lateral size that is approximately 10 times larger than that of MoS2 flakes. One can therefore expect a significant difference in their placement already at the stage of the homogenization process. MoS2 crystals have a similar flake morphology (Figure 2b). They are characterized by an average lateral dimension of 480 nm and a thickness in the range of 20-40 nm.
After weighing, the powders were mixed in a rotary, horizontal mill in the presence of zirconium balls. The mass ratio of balls to powder was 3:1. The process was carried out with isopropyl alcohol for 8 h. The rotational speed was set at 300 rpm, enabling the smallest number of defects to be introduced into the layered crystals. Previous research [28] has shown that during mixing defoliation the formation of much thinner flakes can occur. At the same time, as shown in the Figure 3, bigger aluminum particles experience small deformations (flattening) due to collisions with ZrO2 balls, making a shape similar to a disk. No significant differences were found in the morphology of aluminum particles after the milling process in the presence of various additives. The mixed suspensions were dried and granulated on 0.3 mm mesh screens. The final stage was the powder consolidation, which ran directly in the SPS device (HP D 10, FCT Systeme GmbH, Rauenstein, Germany), realizing a different strain. The process conditions are presented in Table 2. The first option included a classic, one-step process of SPS consolidation in a graphite matrix with a diameter of 20 mm, temperature T = 550 °C, and pressure of 50 MPa. This process was previously optimized to obtain material of the highest density. The final stage was the powder consolidation, which ran directly in the SPS device (HP D 10, FCT Systeme GmbH, Rauenstein, Germany), realizing a different strain. The process conditions are presented in Table 2. The first option included a classic, one-step process of SPS consolidation in a graphite matrix with a diameter of 20 mm, temperature T = 550 • C, and pressure of 50 MPa. This process was previously optimized to obtain material of the highest density. The second variant was a two-stage SPT process. In the first stage, the powder was pre-sintered into a cylinder with a diameter of 20 mm under the small pressure required for the proper operation of the device and using a lower temperature. In the second stage, the previously prepared compact was subjected to the upsetting process in a larger diameter die, to allow the material to flow freely until it was completely filled. A sample with an initial diameter of 20 mm was pressed in a 30 mm die and a 40 mm die. For matrices of different diameters, a different force was used to ensure a constant pressure of 50 MPa.
For simplicity, in the further part of this article we will use the deformation ratio λ = d/d 0 , meaning the ratio of the final diameter (d) of the die to the initial diameter (d 0 ). For the SPS process, the deformation ratio λ = 1 and for SPT λ = 1.5 or 2. The values of the main parameters of the SPT process are listed in Table 2 and the process is schematically shown in Figure 4. For both compositions, an identical material volume was assumed for the same degree of deformation. The initial heights of the stage I samples were 22 and 30 mm according to the deformation ratio.  The second variant was a two-stage SPT process. In the first stage, the powder was pre-sintered into a cylinder with a diameter of 20 mm under the small pressure required for the proper operation of the device and using a lower temperature. In the second stage, the previously prepared compact was subjected to the upsetting process in a larger diameter die, to allow the material to flow freely until it was completely filled. A sample with an initial diameter of 20 mm was pressed in a 30 mm die and a 40 mm die. For matrices of different diameters, a different force was used to ensure a constant pressure of 50 MPa.
For simplicity, in the further part of this article we will use the deformation ratio λ = d/d0, meaning the ratio of the final diameter (d) of the die to the initial diameter (d0). For the SPS process, the deformation ratio λ = 1 and for SPT λ = 1.5 or 2. The values of the main parameters of the SPT process are listed in Table 2 and the process is schematically shown in Figure 4. For both compositions, an identical material volume was assumed for the same degree of deformation. The initial heights of the stage I samples were 22 and 30 mm according to the deformation ratio. The obtained sinters were mechanically ground and polished first with diamond paste down to a grit size of 1 μm and finally with nanosilica suspension. In order to reveal the microstructure, samples were etched with Dix Keller reagent. The powders morphology and microstructure were observed using scanning electron microscopes (Hitachi S3500 and S5500, Japan) as well as a light microscope (NIKON Eclipse MA200, NIKON, Tokyo, Japan). Microstructures and chemical compositions of the samples were examined with a transmission electron microscope (TEM) (FEI, Hillsboro, Oregon, OR, USA) Tecnai G2 operating at 200 kV, equipped with an energy dispersive Xray (EDX) microanalyzer and a high angle annular dark field detector (HAADF). Stereological methods were used for the precise description of powders and structures based on their planar images. The characterization of powders and grain structures was conducted for individual grains/particles and parameters such as: Equivalent average diameter (grain size): d2, maximal projection: dmax, and minimal projection: dmin. Also, the shape factor α = dmax/d2 and was measured. The obtained sinters were mechanically ground and polished first with diamond paste down to a grit size of 1 µm and finally with nanosilica suspension. In order to reveal the microstructure, samples were etched with Dix Keller reagent. The powders morphology and microstructure were observed using scanning electron microscopes (Hitachi S3500 and S5500, Japan) as well as a light microscope (NIKON Eclipse MA200, NIKON, Tokyo, Japan). Microstructures and chemical compositions of the samples were examined with a transmission electron microscope (TEM) (FEI, Hillsboro, Oregon, OR, USA) Tecnai G2 operating at 200 kV, equipped with an energy dispersive X-ray (EDX) microanalyzer and a high angle annular dark field detector (HAADF). Stereological methods were used for the precise description of powders and structures based on their planar images. The characterization of powders and grain structures was conducted for individual grains/particles and parameters such as: Equivalent average diameter (grain size): d 2 , maximal projection: d max , and minimal projection: d min . Also, the shape factor α = d max /d 2 and was measured. These parameters were determined with the planimetric methods and computer image analysis (NIKON NIS-Elements; Tokyo, Japan). Fundamental properties of the obtained materials such as density (Ultrapycnometer 1000 helium pycnometer Quantachrome Instruments, Boynton Beach, FL, USA) and hardness (Vickers Hardness Tester FV-700e, Future-Tech, Kawasaki, Japan) were measured.

Results and Discussion
Upsetting in a closed die is a quite complex process from a mechanical point of view [29]. Its full understanding will involve the analysis of many process parameters such as stresses and strains present in the material along with the influence of the additive volume. This research focused mainly on microstructural issues. The addition of 10 vol % of layered crystals was chosen because of its improvement of the tribological properties, which was described in earlier works [4,22], mainly consisting of the creation of permanent tribofilm and a decrease in the wear rate. The addition of this amount also allows easy tracking of microstructural changes and comparison of test results for different types of additives with different morphologies.

Physical Properties
As a result of running a number of optimization processes for SPS sinters in the case of pure aluminum and the addition of a small amount of layered crystals up to 2 vol %, a high density exceeding 99% is achieved [4]. The proportion of additives exceeding 5% by volume is associated with the presence of a certain amount of pores at the interface and between the additive particles. Then the density of the composite drastically decreases. In the case analyzed, for the 10 vol % process, optimization allowed the achievement of a relative density near 95%. Density measurements for material subjected to SPT processes indicate an improvement for MLG composites up to 98.1%. However, the increase in the deformation ratio has little effect on further improvement of the density (98.2%).
The addition of molybdenum disulfide completely changes the situation and the SPT process, leading to a reduction in the density of composites from 94.8% to 92.1%. Density changes resulting from the production method are shown in Figure 5. These parameters were determined with the planimetric methods and computer image analysis (NIKON NIS-Elements; Tokyo, Japan). Fundamental properties of the obtained materials such as density (Ultrapycnometer 1000 helium pycnometer Quantachrome Instruments, Boynton Beach, FL, USA) and hardness (Vickers Hardness Tester FV-700e, Future-Tech, Kawasaki, Japan) were measured.

Results and Discussion
Upsetting in a closed die is a quite complex process from a mechanical point of view [29]. Its full understanding will involve the analysis of many process parameters such as stresses and strains present in the material along with the influence of the additive volume. This research focused mainly on microstructural issues. The addition of 10 vol % of layered crystals was chosen because of its improvement of the tribological properties, which was described in earlier works [4,22], mainly consisting of the creation of permanent tribofilm and a decrease in the wear rate. The addition of this amount also allows easy tracking of microstructural changes and comparison of test results for different types of additives with different morphologies.

Physical Properties
As a result of running a number of optimization processes for SPS sinters in the case of pure aluminum and the addition of a small amount of layered crystals up to 2 vol %, a high density exceeding 99% is achieved [4]. The proportion of additives exceeding 5% by volume is associated with the presence of a certain amount of pores at the interface and between the additive particles. Then the density of the composite drastically decreases. In the case analyzed, for the 10 vol % process, optimization allowed the achievement of a relative density near 95%. Density measurements for material subjected to SPT processes indicate an improvement for MLG composites up to 98.1%. However, the increase in the deformation ratio has little effect on further improvement of the density (98.2%).
The addition of molybdenum disulfide completely changes the situation and the SPT process, leading to a reduction in the density of composites from 94.8% to 92.1%. Density changes resulting from the production method are shown in Figure 5. Paradoxically, similar differences resulting from the type of additive occur in the hardness of materials and the observed behavior of the material, especially for the addition of molybdenum disulfide.
For the SPS process, the addition of 10 vol % of MLG flakes slightly reduces the hardness from 54 HV1 for the aluminum alloy sinter to 46 HV1 for the composite. The use of the SPT process with a low deformation ratio (λ = 1.5) has very little effect on hardness and leads to its increase to about 47 HV1. Increasing the deformation ratio slightly reduces the hardness to the level of 44.5 HV1.
Composites with the addition of MoS2 flakes behave differently, and when using the SPT process Paradoxically, similar differences resulting from the type of additive occur in the hardness of materials and the observed behavior of the material, especially for the addition of molybdenum disulfide.
For the SPS process, the addition of 10 vol % of MLG flakes slightly reduces the hardness from 54 HV1 for the aluminum alloy sinter to 46 HV1 for the composite. The use of the SPT process with a low deformation ratio (λ = 1.5) has very little effect on hardness and leads to its increase to about 47 HV1. Increasing the deformation ratio slightly reduces the hardness to the level of 44.5 HV1.
Composites with the addition of MoS 2 flakes behave differently, and when using the SPT process there is an especially strong increase in the hardness of the composite. For the highest deformation ratio, the average hardness reaches 76.4 HV1. In this case there is a large standard deviation, which suggests a dispersion of the test value from the average. The examined hardness increase does not correlate with the density changes and can only be explained by microstructure analysis, which will be shown later in the article. The changes in the hardness of the tested composites are shown in Figure 6. there is an especially strong increase in the hardness of the composite. For the highest deformation ratio, the average hardness reaches 76.4 HV1. In this case there is a large standard deviation, which suggests a dispersion of the test value from the average. The examined hardness increase does not correlate with the density changes and can only be explained by microstructure analysis, which will be shown later in the article. The changes in the hardness of the tested composites are shown in Figure 6. Because in practice such processes guarantee the inhomogeneity of stresses and strains [30] in the volume of the material being processed, one can expect far-reaching structure heterogeneities. Therefore, hardness tests were carried out on a cross-section parallel to the direction of the force acting during the sintering process. The hardness was tested from the central area to the edge of the sample on the long axis of this cross-section.
As can be seen in the Figures 7 and 8, composites with MLG content are characterized by significantly better uniformity of hardness on the cross-section than in the case of composites with MoS2. After the SPS process, the middle part of the sinter is slightly harder, which can be the result of the easy migration of powder particles in this area and a slight decrease in the thickness of MLG agglomerates. These changes are not visible in the microstructure. When the possibility of displacement over long distances is realized, the structure is further homogenized. In molybdenum disulfide composite ( Figure 8), a significant increase in hardness is noted, but only in the middle areas of the sample. As we move away from the center, we observe a decrease in hardness. Interestingly, for composites obtained in the SPS process, this type of heterogeneity does not occur and only reveals itself as a result of the SPT process. Because in practice such processes guarantee the inhomogeneity of stresses and strains [30] in the volume of the material being processed, one can expect far-reaching structure heterogeneities. Therefore, hardness tests were carried out on a cross-section parallel to the direction of the force acting during the sintering process. The hardness was tested from the central area to the edge of the sample on the long axis of this cross-section.
As can be seen in the Figures 7 and 8, composites with MLG content are characterized by significantly better uniformity of hardness on the cross-section than in the case of composites with MoS 2 . After the SPS process, the middle part of the sinter is slightly harder, which can be the result of the easy migration of powder particles in this area and a slight decrease in the thickness of MLG agglomerates. These changes are not visible in the microstructure. When the possibility of displacement over long distances is realized, the structure is further homogenized. there is an especially strong increase in the hardness of the composite. For the highest deformation ratio, the average hardness reaches 76.4 HV1. In this case there is a large standard deviation, which suggests a dispersion of the test value from the average. The examined hardness increase does not correlate with the density changes and can only be explained by microstructure analysis, which will be shown later in the article. The changes in the hardness of the tested composites are shown in Figure 6. Because in practice such processes guarantee the inhomogeneity of stresses and strains [30] in the volume of the material being processed, one can expect far-reaching structure heterogeneities. Therefore, hardness tests were carried out on a cross-section parallel to the direction of the force acting during the sintering process. The hardness was tested from the central area to the edge of the sample on the long axis of this cross-section.
As can be seen in the Figures 7 and 8, composites with MLG content are characterized by significantly better uniformity of hardness on the cross-section than in the case of composites with MoS2. After the SPS process, the middle part of the sinter is slightly harder, which can be the result of the easy migration of powder particles in this area and a slight decrease in the thickness of MLG agglomerates. These changes are not visible in the microstructure. When the possibility of displacement over long distances is realized, the structure is further homogenized. In molybdenum disulfide composite (Figure 8), a significant increase in hardness is noted, but only in the middle areas of the sample. As we move away from the center, we observe a decrease in hardness. Interestingly, for composites obtained in the SPS process, this type of heterogeneity does not occur and only reveals itself as a result of the SPT process. In molybdenum disulfide composite (Figure 8), a significant increase in hardness is noted, but only in the middle areas of the sample. As we move away from the center, we observe a decrease in hardness. Interestingly, for composites obtained in the SPS process, this type of heterogeneity does not occur and only reveals itself as a result of the SPT process.

Processing
The charts below (Figures 9 and 10) show a comparison of the second stage of the SPT process for the processing rate λ = 2. In both cases, the same volume of material was used and the process was carried out with the same parameters (force and heating speed). Time differences resulting from the unequal start of the heating process after filling the chamber with protective gas were eliminated in the diagrams. Figure 9 presents a comparison of three measured values: Temperature, speed of punch, and displacement of punch for composites with various types of reinforcement (continuous and dashed curve). Due to the size of the samples (a small volume of material) differences in the curves are almost imperceptible, but enlarging the area to reflect the displacement ( Figure 10) indicates that the composite with MLG is easier to deform and the punch is moved at a higher speed than the composite with MoS2. Similar relationships were observed for the process with λ = 1.5 and their analysis suggests that the effect is proportional to the deformation ratio.

Processing
The charts below (Figures 9 and 10) show a comparison of the second stage of the SPT process for the processing rate λ = 2. In both cases, the same volume of material was used and the process was carried out with the same parameters (force and heating speed). Time differences resulting from the unequal start of the heating process after filling the chamber with protective gas were eliminated in the diagrams. Figure 9 presents a comparison of three measured values: Temperature, speed of punch, and displacement of punch for composites with various types of reinforcement (continuous and dashed curve). Due to the size of the samples (a small volume of material) differences in the curves are almost imperceptible, but enlarging the area to reflect the displacement ( Figure 10) indicates that the composite with MLG is easier to deform and the punch is moved at a higher speed than the composite with MoS 2 . Similar relationships were observed for the process with λ = 1.5 and their analysis suggests that the effect is proportional to the deformation ratio.

Processing
The charts below (Figures 9 and 10) show a comparison of the second stage of the SPT process for the processing rate λ = 2. In both cases, the same volume of material was used and the process was carried out with the same parameters (force and heating speed). Time differences resulting from the unequal start of the heating process after filling the chamber with protective gas were eliminated in the diagrams. Figure 9 presents a comparison of three measured values: Temperature, speed of punch, and displacement of punch for composites with various types of reinforcement (continuous and dashed curve). Due to the size of the samples (a small volume of material) differences in the curves are almost imperceptible, but enlarging the area to reflect the displacement ( Figure 10) indicates that the composite with MLG is easier to deform and the punch is moved at a higher speed than the composite with MoS2. Similar relationships were observed for the process with λ = 1.5 and their analysis suggests that the effect is proportional to the deformation ratio.

Processing
The charts below (Figures 9 and 10) show a comparison of the second stage of the SPT process for the processing rate λ = 2. In both cases, the same volume of material was used and the process was carried out with the same parameters (force and heating speed). Time differences resulting from the unequal start of the heating process after filling the chamber with protective gas were eliminated in the diagrams. Figure 9 presents a comparison of three measured values: Temperature, speed of punch, and displacement of punch for composites with various types of reinforcement (continuous and dashed curve). Due to the size of the samples (a small volume of material) differences in the curves are almost imperceptible, but enlarging the area to reflect the displacement ( Figure 10) indicates that the composite with MLG is easier to deform and the punch is moved at a higher speed than the composite with MoS2. Similar relationships were observed for the process with λ = 1.5 and their analysis suggests that the effect is proportional to the deformation ratio.   Differences in the implementation of the SPT process can also be caused by the different ways in which current flows through the material. Depending on the electrical properties of the specimen, the current flow differs drastically and can affect temperature changes in micro-areas. In the group of additives used, we have a carbon material (multilayer graphene) which has much better electrical and thermal conductivity than the MoS2 semiconductor [31]. Although it is not possible to explicitly exclude the influence of the described factors on the formation process, the authors agree that the effective differences in the obtained properties of the composites are the result of the morphology and mechanical properties of the additives used, which will be proved during microstructure analysis. Therefore, the analysis takes into account the degree of processing and cross-sectional areas differing significantly in microstructure. A detailed analysis of microstructure images should also indicate a specific mechanism of the components' movement (matrix and reinforcement) during SPT processes. Differences in the implementation of the SPT process can also be caused by the different ways in which current flows through the material. Depending on the electrical properties of the specimen, the current flow differs drastically and can affect temperature changes in micro-areas. In the group of additives used, we have a carbon material (multilayer graphene) which has much better electrical and thermal conductivity than the MoS2 semiconductor [31]. Although it is not possible to explicitly exclude the influence of the described factors on the formation process, the authors agree that the effective differences in the obtained properties of the composites are the result of the morphology and mechanical properties of the additives used, which will be proved during microstructure analysis. Therefore, the analysis takes into account the degree of processing and cross-sectional areas differing significantly in microstructure. A detailed analysis of microstructure images should also indicate a specific mechanism of the components' movement (matrix and reinforcement) during SPT processes.    Differences in the implementation of the SPT process can also be caused by the different ways in which current flows through the material. Depending on the electrical properties of the specimen, the current flow differs drastically and can affect temperature changes in micro-areas. In the group of additives used, we have a carbon material (multilayer graphene) which has much better electrical and thermal conductivity than the MoS2 semiconductor [31]. Although it is not possible to explicitly exclude the influence of the described factors on the formation process, the authors agree that the effective differences in the obtained properties of the composites are the result of the morphology and mechanical properties of the additives used, which will be proved during microstructure analysis. Therefore, the analysis takes into account the degree of processing and cross-sectional areas differing significantly in microstructure. A detailed analysis of microstructure images should also indicate a specific mechanism of the components' movement (matrix and reinforcement) during SPT processes.    In both cases of the composite materials (Figures 12 and 13), we observe a series of heterogeneities indicating the effects of the homogenization process. Flakes of layered crystals with transverse dimensions of the order of nanometers agglomerate, and the final form of agglomerates in the sinter reaches the order of micrometers. In both cases, there is also a characteristic arrangement or orientation of powder particles. MLG flakes/agglomerates with large lateral dimensions are arranged perpendicularly to the direction of the applied force, while fine MoS2 flakes "coat" the aluminum particles tightly and it is difficult to distinguish the preferred direction of their placement. The stereological analysis indicates that the addition of MLG did not affect the size of the aluminum grain (d2 = 10.3 μm), while the addition of MoS2 caused a reduction in the average grain size in the matrix (d2 = 8.8 μm) in relation to sinters without additions.

Microstructure
The details of the platelets' placement are important for the analysis of the SPT process, but also give an overview of the results of density measurements. Figure 14 shows distribution of individual flakes of the second phase. As can be seen, the obtained porosity is mainly the result of insufficient space filling by layered crystals which, through their morphology and the fact of the presence on the boundaries of aluminum powder particles, generate a large amount of nanopores, translating into a fairly high total porosity of 5%. The materials obtained in the SPS process did not show any clear deviations in the microstructure over the entire cross-section. In the case of SPT sinters, a number of areas characterized by specific structural features were found as well as clear differences resulting from the location along the axis of the cross-section parallel to the direction of the pressing. For statistical purposes, in the stereological calculations, typical places from the center and near the edge areas located in cross-section were taken into account and compared. In both cases of the composite materials (Figures 12 and 13), we observe a series of heterogeneities indicating the effects of the homogenization process. Flakes of layered crystals with transverse dimensions of the order of nanometers agglomerate, and the final form of agglomerates in the sinter reaches the order of micrometers. In both cases, there is also a characteristic arrangement or orientation of powder particles. MLG flakes/agglomerates with large lateral dimensions are arranged perpendicularly to the direction of the applied force, while fine MoS 2 flakes "coat" the aluminum particles tightly and it is difficult to distinguish the preferred direction of their placement. The stereological analysis indicates that the addition of MLG did not affect the size of the aluminum grain (d 2 = 10.3 µm), while the addition of MoS 2 caused a reduction in the average grain size in the matrix (d 2 = 8.8 µm) in relation to sinters without additions.
The details of the platelets' placement are important for the analysis of the SPT process, but also give an overview of the results of density measurements. Figure 14 shows distribution of individual flakes of the second phase. As can be seen, the obtained porosity is mainly the result of insufficient space filling by layered crystals which, through their morphology and the fact of the presence on the boundaries of aluminum powder particles, generate a large amount of nanopores, translating into a fairly high total porosity of 5%. In both cases of the composite materials (Figures 12 and 13), we observe a series of heterogeneities indicating the effects of the homogenization process. Flakes of layered crystals with transverse dimensions of the order of nanometers agglomerate, and the final form of agglomerates in the sinter reaches the order of micrometers. In both cases, there is also a characteristic arrangement or orientation of powder particles. MLG flakes/agglomerates with large lateral dimensions are arranged perpendicularly to the direction of the applied force, while fine MoS2 flakes "coat" the aluminum particles tightly and it is difficult to distinguish the preferred direction of their placement. The stereological analysis indicates that the addition of MLG did not affect the size of the aluminum grain (d2 = 10.3 μm), while the addition of MoS2 caused a reduction in the average grain size in the matrix (d2 = 8.8 μm) in relation to sinters without additions.
The details of the platelets' placement are important for the analysis of the SPT process, but also give an overview of the results of density measurements. Figure 14 shows distribution of individual flakes of the second phase. As can be seen, the obtained porosity is mainly the result of insufficient space filling by layered crystals which, through their morphology and the fact of the presence on the boundaries of aluminum powder particles, generate a large amount of nanopores, translating into a fairly high total porosity of 5%. The materials obtained in the SPS process did not show any clear deviations in the microstructure over the entire cross-section. In the case of SPT sinters, a number of areas characterized by specific structural features were found as well as clear differences resulting from the location along the axis of the cross-section parallel to the direction of the pressing. For statistical purposes, in the stereological calculations, typical places from the center and near the edge areas located in cross-section were taken into account and compared. The materials obtained in the SPS process did not show any clear deviations in the microstructure over the entire cross-section. In the case of SPT sinters, a number of areas characterized by specific structural features were found as well as clear differences resulting from the location along the axis of the cross-section parallel to the direction of the pressing. For statistical purposes, in the stereological calculations, typical places from the center and near the edge areas located in cross-section were taken into account and compared.
The deformation of the pre-sintered compact induced in the SPT process causes the displacement of the composite components. Theoretical investigation also showed that the free upsetting mode generated extra shear strain components which could facilitate the mass transport within the porous specimens [27]. Because the second phase has the possibility of easy delamination, this reduces the friction of shifting crystals (particles of metal alloy powder and the layered crystals themselves). The complex state of stress in the bulk specimen means that aluminum powder particles may experience revolutions and displacements in parallel and perpendicular directions to the applied force. Due to the temperature of the process close to the melting temperature of aluminum (T hom ∼ = 0.8), metal powder particles can also easily change their shape during plastic deformation. In the initial phase of deformation, a large amount of layered crystals at the particle boundaries can easily change their positions and the thickness of the agglomerates changes as well.
In the composites with the addition of MLG, the displacement in the direction of tangential stresses to the direction of the force initially prevails. This is evidenced by the microstructure images from the middle areas of the sample (Figure 15a). Areas rich in MLG are characterized by a morphological texture typical of the material after rolling. The band of graphene flakes on the cross-section is arranged perpendicular to the direction of pressure. As a result of delamination, the average thickness of MLG agglomerates decreases when compared to composites produced in the SPS process from 8.6 µm to 3.5 µm. Along with the displacement, the plastic deformation of the matrix begins and the aluminum grains extend in the direction perpendicular to the pressure force, as evidenced by shape factors from the middle areas of the sample (α = 1.7). It can be assumed that reducing the thickness of the MLG agglomerates will contribute to limiting the displacements towards tangential stresses. Meanwhile, in areas distant from the specimen center (Figure 15b), the MLG agglomerates change their position in a direction parallel to the force direction. The shape coefficient of the aluminum grain (α = 1.4) indicates that the particles are more spherical. In these areas the aluminum particles can more easily rotate and the plastic deformation is lower. The deformation of the pre-sintered compact induced in the SPT process causes the displacement of the composite components. Theoretical investigation also showed that the free upsetting mode generated extra shear strain components which could facilitate the mass transport within the porous specimens [27]. Because the second phase has the possibility of easy delamination, this reduces the friction of shifting crystals (particles of metal alloy powder and the layered crystals themselves). The complex state of stress in the bulk specimen means that aluminum powder particles may experience revolutions and displacements in parallel and perpendicular directions to the applied force. Due to the temperature of the process close to the melting temperature of aluminum (Thom ≅ 0.8), metal powder particles can also easily change their shape during plastic deformation. In the initial phase of deformation, a large amount of layered crystals at the particle boundaries can easily change their positions and the thickness of the agglomerates changes as well.
In the composites with the addition of MLG, the displacement in the direction of tangential stresses to the direction of the force initially prevails. This is evidenced by the microstructure images from the middle areas of the sample (Figure 15a). Areas rich in MLG are characterized by a morphological texture typical of the material after rolling. The band of graphene flakes on the crosssection is arranged perpendicular to the direction of pressure. As a result of delamination, the average thickness of MLG agglomerates decreases when compared to composites produced in the SPS process from 8.6 μm to 3.5 μm. Along with the displacement, the plastic deformation of the matrix begins and the aluminum grains extend in the direction perpendicular to the pressure force, as evidenced by shape factors from the middle areas of the sample (α = 1.7). It can be assumed that reducing the thickness of the MLG agglomerates will contribute to limiting the displacements towards tangential stresses. Meanwhile, in areas distant from the specimen center (Figure 15b), the MLG agglomerates change their position in a direction parallel to the force direction. The shape coefficient of the aluminum grain (α = 1.4) indicates that the particles are more spherical. In these areas the aluminum particles can more easily rotate and the plastic deformation is lower.  With a greater degree of processing when λ = 2 in the center areas of the specimen cross-section, we observe a disturbance of the characteristic rolling texture. Although aluminum grains are still elongated (α = 1.6) (Figure 15c), graphene flakes do not show a clear orientation perpendicular to the force direction, and the average grain size of the metallic phase decreases to 7.1 µm. The reason for the reduction of aluminum grains may be a higher value of deformation and related processes of dynamic recrystallization. In areas distant from the center, the direction of the material flow also changes. The general trend is represented by the deviation of the long grain axis from the direction perpendicular to the pressing force (Figure 15d). The stereological parameters quantitatively describing the differences in the microstructure of the tested materials are presented in Table 3. Table 3. Stereological parameters of composite structures after SPS and SPT processes, SD: Standard deviation.  A slightly different situation is observed for composites with molybdenum disulfide (Figure 16). The deformation of the pre-sintered material causes movement in the MoS 2 flakes relative to each other and the aluminum powder particles, but this movement is not directed. Because the flakes are not oriented in the structure, as in the case of MLG, and form an almost homogeneous barrier around Al particles, their displacement is statistically random. This entails a higher probability of rotation of the aluminum powder particles and leads to the homogenization of large areas containing the agglomerated MoS 2 flakes visible in Figure 13a. The thickness of the MoS 2 agglomerates observed at the grain boundary increases slightly and the boundary formed by them becomes more irregular. This is due to the fact that the platelets moving irregularly generate additional porosity, as detailed in Figure 17. The microstructure confirms the results of the density measurements presented earlier. With a greater degree of processing when λ = 2 in the center areas of the specimen cross-section, we observe a disturbance of the characteristic rolling texture. Although aluminum grains are still elongated (α = 1.6) (Figure 15c), graphene flakes do not show a clear orientation perpendicular to the force direction, and the average grain size of the metallic phase decreases to 7.1 μm. The reason for the reduction of aluminum grains may be a higher value of deformation and related processes of dynamic recrystallization. In areas distant from the center, the direction of the material flow also changes. The general trend is represented by the deviation of the long grain axis from the direction perpendicular to the pressing force (Figure 15d). The stereological parameters quantitatively describing the differences in the microstructure of the tested materials are presented in Table 3. A slightly different situation is observed for composites with molybdenum disulfide (Figure 16). The deformation of the pre-sintered material causes movement in the MoS2 flakes relative to each other and the aluminum powder particles, but this movement is not directed. Because the flakes are not oriented in the structure, as in the case of MLG, and form an almost homogeneous barrier around Al particles, their displacement is statistically random. This entails a higher probability of rotation of the aluminum powder particles and leads to the homogenization of large areas containing the agglomerated MoS2 flakes visible in Figure 13a. The thickness of the MoS2 agglomerates observed at the grain boundary increases slightly and the boundary formed by them becomes more irregular. This is due to the fact that the platelets moving irregularly generate additional porosity, as detailed in Figure 17. The microstructure confirms the results of the density measurements presented earlier.  In the middle areas of the sinters, the grains of the matrix are flattened (Figure 16a) in the direction perpendicular to the force (α = 1.8). The value of the shape coefficient suggests that the ability to displace aluminum particles during the SPT process is more limited and the stresses present in the material in this area cause a greater deformation of the metallic matrix. On the other hand, the aluminum grains on the edge of the sinters are characterized by greater sphericity and have a smaller size (α = 1.4 d2 = 5.8/6.3), according to the deformation ratio (Figure 16b,d). During deformation under conditions of increased friction, smaller particles (with more regular shapes close to the sphere) of aluminum powder are easier to "push" into the edge areas, and are subjected to less deformation at the same time.
The most interesting fact related to the deformation process is the presence of bright places inside the aluminum grains in the central areas ( Figure 17). Chemical analysis indicates that these areas contain elements that do not constitute alloying elements of the aluminum alloy and are characterized by fairly regular shapes in the cross-section, visible as polyhedrons that seem to "grow" from the interface inside the aluminum grain.
The chemical analysis of the described places is shown in Figure 18. Peaks marked as Cu come from the specimen holder. The brightest areas marked 1 represent elements such as Mo and S, which originate from the MoS2 phase located on the borders of the metallic powder particles. However, the presence of aluminum was also found in this place. The area marked 2 is the place inside the grain of the aluminum alloy in which the presence of aluminum was identified. In the area marked 3, also inside the aluminum alloy grain, aluminum and molybdenum were found and this is a clearly different composition compared to the remaining grain part.  In the middle areas of the sinters, the grains of the matrix are flattened (Figure 16a) in the direction perpendicular to the force (α = 1.8). The value of the shape coefficient suggests that the ability to displace aluminum particles during the SPT process is more limited and the stresses present in the material in this area cause a greater deformation of the metallic matrix. On the other hand, the aluminum grains on the edge of the sinters are characterized by greater sphericity and have a smaller size (α = 1.4 d2 = 5.8/6.3), according to the deformation ratio (Figure 16b,d). During deformation under conditions of increased friction, smaller particles (with more regular shapes close to the sphere) of aluminum powder are easier to "push" into the edge areas, and are subjected to less deformation at the same time.
The most interesting fact related to the deformation process is the presence of bright places inside the aluminum grains in the central areas ( Figure 17). Chemical analysis indicates that these areas contain elements that do not constitute alloying elements of the aluminum alloy and are characterized by fairly regular shapes in the cross-section, visible as polyhedrons that seem to "grow" from the interface inside the aluminum grain.
The chemical analysis of the described places is shown in Figure 18. Peaks marked as Cu come from the specimen holder. The brightest areas marked 1 represent elements such as Mo and S, which originate from the MoS2 phase located on the borders of the metallic powder particles. However, the presence of aluminum was also found in this place. The area marked 2 is the place inside the grain of the aluminum alloy in which the presence of aluminum was identified. In the area marked 3, also inside the aluminum alloy grain, aluminum and molybdenum were found and this is a clearly different composition compared to the remaining grain part. In the middle areas of the sinters, the grains of the matrix are flattened (Figure 16a) in the direction perpendicular to the force (α = 1.8). The value of the shape coefficient suggests that the ability to displace aluminum particles during the SPT process is more limited and the stresses present in the material in this area cause a greater deformation of the metallic matrix. On the other hand, the aluminum grains on the edge of the sinters are characterized by greater sphericity and have a smaller size (α = 1.4 d 2 = 5.8/6.3), according to the deformation ratio (Figure 16b,d). During deformation under conditions of increased friction, smaller particles (with more regular shapes close to the sphere) of aluminum powder are easier to "push" into the edge areas, and are subjected to less deformation at the same time.
The most interesting fact related to the deformation process is the presence of bright places inside the aluminum grains in the central areas ( Figure 17). Chemical analysis indicates that these areas contain elements that do not constitute alloying elements of the aluminum alloy and are characterized by fairly regular shapes in the cross-section, visible as polyhedrons that seem to "grow" from the interface inside the aluminum grain.
The chemical analysis of the described places is shown in Figure 18. Peaks marked as Cu come from the specimen holder. The brightest areas marked 1 represent elements such as Mo and S, which originate from the MoS 2 phase located on the borders of the metallic powder particles. However, the presence of aluminum was also found in this place. The area marked 2 is the place inside the grain of the aluminum alloy in which the presence of aluminum was identified. In the area marked 3, also inside the aluminum alloy grain, aluminum and molybdenum were found and this is a clearly different composition compared to the remaining grain part. More precise TEM and electron diffraction studies ( Figure 19) indicate the presence of a new phase in the bright areas. The Al12Mo phase crystallizes in composites in the form of regular areas ranging from a few to over a dozen micrometers. The crystal structure and lattice parameters of Al12Mo, which is the most Al-rich intermetallic phase, were determined by Adam and Rich [32] and Walford [33], as well as confirmed in other works. In equilibrium conditions, its peritectic formation temperature was determined to be 680-700 °C. The inclusions of intermetallic phases such Al12Mo contribute to an increase of hardness in casting Al alloys [34] and rapidly hardened aluminum alloys (RHA) [35]. Clearly, therefore, the increase in hardness observed in composites is the result of the presence of the newly formed phase. Hardness distribution and microstructure observations indicate an increased volume of Al12Mo phase in composites subject to stronger deformation.
At the moment, there are no studies that can confirm the possibility of this phase's formation in composite materials in similar conditions. Although the thermal decomposition of MoS2 takes place at temperatures close to 1200 °C [36], it is possible that the conditions of the sintering process, in particular the high-current electric pulses and state of stress, contribute to significant deviations from the equilibrium state. We cannot exclude the presence of impurities, mainly in the form of moisture adsorbed at the powder preparation stage that affects the course of chemical reactions. There are More precise TEM and electron diffraction studies ( Figure 19) indicate the presence of a new phase in the bright areas. The Al 12 Mo phase crystallizes in composites in the form of regular areas ranging from a few to over a dozen micrometers. The crystal structure and lattice parameters of Al 12 Mo, which is the most Al-rich intermetallic phase, were determined by Adam and Rich [32] and Walford [33], as well as confirmed in other works. In equilibrium conditions, its peritectic formation temperature was determined to be 680-700 • C. The inclusions of intermetallic phases such Al 12 Mo contribute to an increase of hardness in casting Al alloys [34] and rapidly hardened aluminum alloys (RHA) [35]. Clearly, therefore, the increase in hardness observed in composites is the result of the presence of the newly formed phase. Hardness distribution and microstructure observations indicate an increased volume of Al 12 Mo phase in composites subject to stronger deformation.
At the moment, there are no studies that can confirm the possibility of this phase's formation in composite materials in similar conditions. Although the thermal decomposition of MoS 2 takes place at temperatures close to 1200 • C [36], it is possible that the conditions of the sintering process, in particular the high-current electric pulses and state of stress, contribute to significant deviations from the equilibrium state. We cannot exclude the presence of impurities, mainly in the form of moisture adsorbed at the powder preparation stage that affects the course of chemical reactions. There are known literature reports showing the possible reaction and degradation of MoS 2 in the presence of water [37]. The smell of the samples immediately after sintering suggests that small amounts of hydrogen sulfide are released during the process, which are evidence of the MoS 2 decomposition.  [37]. The smell of the samples immediately after sintering suggests that small amounts of hydrogen sulfide are released during the process, which are evidence of the MoS2 decomposition. By analyzing the rich MoS2 area (Figure 19b) in the composites after the SPT process, we can see a significant fragmentation of platelets and the presence of small Al12Mo precipitates in the vicinity of the aluminum grains. The fragmentation of MoS2 is one of the factors influencing the possibility of chemical reaction with aluminum. The second factor is certainly the time of the process sustained for highly deformed composites. The longer processing time allows the diffusion necessary to create a new phase. Taking into account the influence of current pulses and pressure, temperature may rise locally and reach the melting point, which will further affect the observed phenomenon. Consideration of the presence of a new phase will certainly affect the results of relative density, but the estimated calculations indicate changes of no more than 1%.

Conclusions
Application of the SPS process to consolidate AA6061 aluminum powder or composites gives very good results in the form of high density material and good mechanical properties, which is confirmed both by literature reports and the authors' own work. The possibility of producing useful composite materials in the powder metallurgy process is very often limited by the use of appropriate consolidation techniques and starting powders with a specific morphology. The SPS method, like other techniques, may be insufficient in the case of a high-volume fraction of the second phase particles where the main problem is to obtain a high density. During the implementation of this work, it was proposed to use a modified SPS process based on the deformation of the pre-sintered samples, By analyzing the rich MoS 2 area (Figure 19b) in the composites after the SPT process, we can see a significant fragmentation of platelets and the presence of small Al 12 Mo precipitates in the vicinity of the aluminum grains. The fragmentation of MoS 2 is one of the factors influencing the possibility of chemical reaction with aluminum. The second factor is certainly the time of the process sustained for highly deformed composites. The longer processing time allows the diffusion necessary to create a new phase. Taking into account the influence of current pulses and pressure, temperature may rise locally and reach the melting point, which will further affect the observed phenomenon. Consideration of the presence of a new phase will certainly affect the results of relative density, but the estimated calculations indicate changes of no more than 1%.

Conclusions
Application of the SPS process to consolidate AA6061 aluminum powder or composites gives very good results in the form of high density material and good mechanical properties, which is confirmed both by literature reports and the authors' own work. The possibility of producing useful composite materials in the powder metallurgy process is very often limited by the use of appropriate consolidation techniques and starting powders with a specific morphology. The SPS method, like other techniques, may be insufficient in the case of a high-volume fraction of the second phase particles where the main problem is to obtain a high density. During the implementation of this work, it was proposed to use a modified SPS process based on the deformation of the pre-sintered samples, similar to upsetting processes. A modified process called SPT was successfully applied.
Conducting the SPT process for composites with multilayer graphene and MoS 2 crystals addition, representing different morphologies, led to extremely different effects. In both cases, a more or less heterogeneous strain led to different arrangements and changes in the morphology of the layered crystals platelets by defoliation and/or fragmentation.
Composites with MLG addition subjected to the SPT process exhibited an increased density and a slightly increased hardness. The microstructure of such composites was quite homogeneous, although there was a characteristic orientation of the flakes which resulted directly from their shape and axial pressure during the formation process. The process in each case led to the reduction of the MLG agglomerates thickness by their mechanical defoliation. It was found that increasing the deformation ratio does not improve the hardness, but disturbs the orientation of graphene flakes which may affect the composite physical properties such as thermal and electrical conductivity.
Composites with MoS 2 flakes subjected to the SPT process reduced their density by the heterogeneous displacement of MoS 2 platelets, which was primarily the result of their shape and arrangement relative to aluminum particles. On a larger scale, homogenization of the structure also occurred. However, due to the displacement of the layered crystal particles, a large porosity was generated at the nanoscale. An increase in the hardness of the sinters resulted from the in situ formation of the intermetallic phase. The intermetallic phase was formed by the reactions of the metallic matrix with the fragmented MoS 2 crystals in the central regions of the sinter. This phenomenon was directly responsible for the increasing hardness of the composite and the variable hardness of the cross-section. Increasing the deformation ratio led to increased volume share of the created Al 12 Mo phase and hardness, but also to increased porosity.
The morphology of additives is crucial in the compaction process of the examined composites. Other factors affecting the final form of composite include the physical properties of layered crystals such as: Friction/cohesion forces within layered crystals and between components, thermal and electrical conductivity, and chemical properties leading to the reaction between components of the composite. Although they may be very important, their impact in the conducted experiment was not explained and requires further work.
Author Contributions: M.K. was responsible for planning the experiments, writing the article, and data analysis. M.P. performed the SPS sintering experiments. T.C. and J.W. contributed material preparation and SEM observations. A.O. was responsible for data analysis and final corrections.

Conflicts of Interest:
The authors declare no conflict of interest.