Additive Manufacturing of a 316L Steel Matrix Composite Reinforced with CeO2 Particles: Process Optimization by Adjusting the Laser Scanning Speed

The synthesis of novel materials by additive manufacturing requires the optimization of the processing parameters in order to obtain fully-dense defect-free specimens. This step is particularly important for processing of composite materials, where the addition of a second phase may significantly alter the melting and solidification steps. In this work, a composite consisting of a 316L steel matrix and 5 vol.% CeO2 particles was fabricated by selective laser melting (SLM). The SLM parameters leading to a defect-free 316L matrix are not suitable for the production of 316L/CeO2 composite specimens. However, highly-dense composite samples can be synthesized by carefully adjusting the laser scanning speed, while keeping the other parameters constant. The addition of the CeO2 reinforcement does not alter phase formation, but it affects the microstructure of the composite, which is significantly refined compared with the unreinforced 316L material.


Introduction
Material synthesis by additive manufacturing (AM) has recently emerged as a flexible processing tool for the fabrication of components with intricate geometries and superior properties [1].Among the different AM technologies, selective laser melting (SLM) represents an optimal choice for the production of highly-dense metallic parts because of the use of high-energy laser beams capable to fuse/weld metallic particles layer by layer [2,3].Additionally, SLM processing leads to remarkable differences in terms of microstructures and properties compared with conventional manufacturing processes, like casting [4][5][6].High temperature gradients, fast moving of the laser beam, and rapid solidification are characteristic features of SLM, which can crucially affect microstructures and properties of the SLM parts [2,7].
A wide variety of materials, including Al-based alloys, steels, and metallic glasses [5,7,8], has been fabricated by SLM.In particular, 316L steel synthesized by SLM has been extensively investigated because of its excellent corrosion and oxidation resistance under severe environments [9][10][11].Recent efforts have been focused on the fabrication of stainless steel matrix composites [12,13].For example, AlMangour et al. [14,15] studied the effect of powder preparation as well as of size and volume fraction of TiC reinforcements on the microstructure and mechanical properties of 316L, while Hao et al. [16] and Wei et al. [17] optimized the SLM processing parameters to fabricate a hydroxyapatite/316L composite.The addition of reinforcing particles-such as SiC, TiC, TiB 2 , and Al 2 O 3 -to stainless steel can further enhance mechanical and wear properties at moderate and high temperatures, and expand the range of potential applications of these composites to aerospace and biomedical industries [18,19].
Two main features play a decisive role for determining the final microstructure and the mechanical properties of composites synthesized by SLM: the first is related to the processing parameters, such as laser power, laser scan speed, hatch distance, hatch layer thickness, and laser spot size [20] and the second is associated with the characteristics of the reinforcing particles, including particle size and morphology, and their dispersion within the matrix [21].A uniform distribution of the reinforcing particles in a matrix-reinforcement powder mixture is a prerequisite for its homogeneous distribution in the final bulk composite.Ball milling can be successfully used for the preparation of homogeneous particle mixtures.The uniform distribution of the reinforcement achieved by ball milling, however, it is usually accompanied by a change of the powder morphology resulting from the high energy impacts between particles and milling media [22,23], which in turn may influence the solidification characteristics and the properties of the composite material after SLM [23].
Due to the addition of the second phase and the change of the powder morphology, the SLM processing parameters leading to defect-free specimens of the unreinforced matrix might not be suitable for the synthesis of fully-dense composites and the optimization of the parameters might be necessary [24][25][26].Accordingly, the objective of this work is the optimization of the SLM processing parameters to produce defect-free 316L matrix composites reinforced with 5 vol.%CeO 2 particles.To achieve this aim, different scanning speeds have been employed and the resulting phases, microstructures and densification of the SLM parts have been investigated.The present steel-matrix composite belongs to the family of oxide dispersion strengthened (ODS) alloys, where oxide particles, such as Y 2 O 3 , CeO 2 , Al 2 O 3 , and TiO 2 [27], are dispersed into a metallic matrix in order to achieve elevated temperature strength, creep, and resistance against radiation [28,29].

Materials and Methods
Gas-atomized 316L stainless steel powder (Realizer GmbH) with spherical morphology and average particle size of 36 µm (Figure 1a,b) and CeO 2 powder (chemPUR) with size in the range of 0.5-1 µm were used for the present experiments.Composite powder mixtures consisting of the 316L matrix and 5 vol.%CeO 2 were prepared by ball milling in order to ensure the homogeneous distribution of the reinforcing phase.Ball milling was carried out for 2 h using a Retsch PM 400 (Retsch, Haan, Germany) planetary ball mill with hardened steel vials and balls at a ball-to-powder weight ratio of 6:1 and a milling velocity of 100 rpm.To avoid an excessive temperature rise inside the vial during milling, the rotation was paused for 15 min after every 15 min milling.SLM processing was performed using an SLM 250 HL device (SLM Solutions, Lübeck, Germany) equipped with a Yb-YAG laser.Cylindrical samples with 3.5 mm diameter and 7 mm length were built on a 316L substrate plate using the following parameters: laser power 175 W, layer thickness 30 µm, hatch spacing 120 µm, and hatch style rotation 79 • .The scanning speed was varied in the range of 250-688 mm/s (688 mm/s being the optimized speed for the single-phase 316L).In order to minimize oxygen contamination, SLM processing was carried out under high purity argon atmosphere.Phase analysis was performed by X-ray diffraction (XRD) using a D3290 PANalytical X' PRO diffractometer with Co-Kα radiation (λ = 0.17889 nm).The density of the samples was measured by the Archimedes principle and by X-ray computed tomography (XCT).XCT scans with voxel size of 5 µm were carried out using a General Electric Phoenix Nanotom m device (General Electric, New York, NY, USA).The microstructure of the samples was investigated by scanning electron microscopy (SEM; Leo Gemini 1530, Carl Zeiss, Jena, Germany).Samples for SEM investigations were mechanically polished and chemically etched at room temperature for 7 min using an acidic water solution containing 2% HF and 8% HNO 3 .The size distributions of the particles and cells were evaluated from the SEM micrographs by using the image analysis software ImageJ 1.X.Crystallographic orientation and grain size of the SLM samples were studied by EBSD (Brooker esprit, detector e flash-HR) using the ESPRIT.2.1 CrystAlign software [30].The step size of the EBSD measurement was 1 µm.For EBSD mapping, the unreinforced 316L matrix and composite samples were sectioned along the Y-Z plane (with X building direction).Room temperature quasistatic compression tests (strain rate = 8 × 10 −5 s −1 ) were performed on cylindrical samples (7 mm length and 3.5 mm diameter) of the unreinforced 316L and 316L/CeO 2 composites using an Instron 5869 testing facility.The strain was measured directly on the samples using a Fiedler laser-extensometer.The compression tests for all specimens were intentionally stopped at 15% strain.A total of 10 specimens for unreinforced matrix and composite were tested in order to ensure the reproducibility of the results.(with X building direction).Room temperature quasistatic compression tests (strain rate = 8 × 10 −5 s −1 ) were performed on cylindrical samples (7 mm length and 3.5 mm diameter) of the unreinforced 316L and 316L/CeO2 composites using an Instron 5869 testing facility.The strain was measured directly on the samples using a Fiedler laser-extensometer.The compression tests for all specimens were intentionally stopped at 15% strain.A total of 10 specimens for unreinforced matrix and composite were tested in order to ensure the reproducibility of the results.

Results and Discussion
The optimized SLM parameters for the unreinforced 316L matrix (scanning speed 688 mm/s, laser power 175 W, layer thickness 30 µm, hatch spacing 120 µm, and hatch style rotation 79°) provide highly-dense specimens with a relative density of 99.9%, as demonstrated by the corresponding results in Figures 2a and Figure 3a.On the other hand, the same parameters are not suitable for SLM processing of the 316L/CeO2 powder mixture: the composite material is highly porous (relative density ~94%) with the CeO2 phase (bright contrast in Figure 3b) mostly located at the interface between matrix and pores.Two main differences, which can explain this behavior, exist in the processing of the unreinforced matrix and 316L/CeO2 powders: (i) the milling step used for the preparation of the homogeneous 316L/CeO2 powder mixture and (ii) the presence of the CeO2 second phase.
Milling can induce a significant change in the size and morphology of the powder, which in turn may influence the melting and solidification steps.Indeed, milling for 2 h drastically increases the size of the unreinforced 316L powder so that defect-free specimens can no longer be synthesized using the optimized parameters (not shown here).On the other hand, milling the 316L/CeO2 powder mixture only slightly reduces the particle size compared to the as-atomized powder (Figure 1c,d).The effect of milling can, therefore, be neglected.

Results and Discussion
The optimized SLM parameters for the unreinforced 316L matrix (scanning speed 688 mm/s, laser power 175 W, layer thickness 30 µm, hatch spacing 120 µm, and hatch style rotation 79 • ) provide highly-dense specimens with a relative density of 99.9%, as demonstrated by the corresponding results in Figures 2a and 3a.On the other hand, the same parameters are not suitable for SLM processing of the 316L/CeO 2 powder mixture: the composite material is highly porous (relative density ~94%) with the CeO 2 phase (bright contrast in Figure 3b) mostly located at the interface between matrix and pores.Two main differences, which can explain this behavior, exist in the processing of the unreinforced matrix and 316L/CeO 2 powders: (i) the milling step used for the preparation of the homogeneous 316L/CeO 2 powder mixture and (ii) the presence of the CeO 2 second phase.
Milling can induce a significant change in the size and morphology of the powder, which in turn may influence the melting and solidification steps.Indeed, milling for 2 h drastically increases the size of the unreinforced 316L powder so that defect-free specimens can no longer be synthesized using the optimized parameters (not shown here).On the other hand, milling the 316L/CeO 2 powder mixture only slightly reduces the particle size compared to the as-atomized powder (Figure 1c,d).The effect of milling can, therefore, be neglected.The addition to the CeO2 second phase most likely has the strongest impact for affecting powder melting and the subsequent solidification process.The presence of the CeO2 particles on the surface of the 316L particles (Figure 3c) may absorb some of the laser energy input, making the energy insufficient to entirely melt the 316L particles.This behavior may preferentially raise the temperature on the particles surface, leading to surface melting, while the particle cores are still solid.Through this mechanism, necks are formed between the particles; however, due to the fast movement of the laser beam, the particles are only partially joined together and pores between solidified metallic agglomerates are left behind [32].
The use of a low laser power or a fast laser scanning speed usually leads to higher porosity during laser processing of 316L stainless steel [32].Under these conditions, the energy input is decreased and the volume of the melt pool becomes smaller, leading to a discontinuous scan track   The addition to the CeO2 second phase most likely has the strongest impact for affecting powder melting and the subsequent solidification process.The presence of the CeO2 particles on the surface of the 316L particles (Figure 3c) may absorb some of the laser energy input, making the energy insufficient to entirely melt the 316L particles.This behavior may preferentially raise the temperature on the particles surface, leading to surface melting, while the particle cores are still solid.Through this mechanism, necks are formed between the particles; however, due to the fast movement of the laser beam, the particles are only partially joined together and pores between solidified metallic agglomerates are left behind [32].
The use of a low laser power or a fast laser scanning speed usually leads to higher porosity during laser processing of 316L stainless steel [32].Under these conditions, the energy input is decreased and the volume of the melt pool becomes smaller, leading to a discontinuous scan track The addition to the CeO 2 second phase most likely has the strongest impact for affecting powder melting and the subsequent solidification process.The presence of the CeO 2 particles on the surface of the 316L particles (Figure 3c) may absorb some of the laser energy input, making the energy insufficient to entirely melt the 316L particles.This behavior may preferentially raise the temperature on the particles surface, leading to surface melting, while the particle cores are still solid.Through this mechanism, necks are formed between the particles; however, due to the fast movement of the laser beam, the particles are only partially joined together and pores between solidified metallic agglomerates are left behind [31].
The use of a low laser power or a fast laser scanning speed usually leads to higher porosity during laser processing of 316L stainless steel [31].Under these conditions, the energy input is decreased and the volume of the melt pool becomes smaller, leading to a discontinuous scan track smaller than the laser spot and to the occurrence of the balling phenomenon [32][33][34][35], where the laser penetration depth is not deep enough to weld the neighboring layers [36].To overcome this problem, the decrease of the laser scanning speed is recommended to achieve higher densification levels in SLM parts [37].Lower scanning speeds, and thus the increase of the laser energy input, create a large melt pool and more powder particles are melted [38].
The scanning speed should be selected carefully in order to provide sufficient energy input capable to create a continuous track of molten liquid and a fully dense surface after solidification.The density of CeO 2 (7.65 g/m 3 ) is slightly lower than that of 316L (8 g/m 3 ) [39] and, consequently, the scanning speed should be fast enough to shorten the solidification time without giving the reinforcement particles time for floating on the top of the melt pool [17].Decreasing the scanning speed to 350 mm/s, while keeping the other parameters constant, increases the relative density to 98% (Figure 2b); unfortunately, the CeO 2 particles are not homogeneously distributed and are mainly located at the edges of the sample.At such a low scanning speed, a large temperature gradient may exist between the center and the edge of the melt pool [40].This may lead to a higher surface tension at the cooler edge, which may then be accompanied by the outward flow of the 2 particles from the hot liquid to the edge of the pool, explaining the behavior observed in Figure 2b.This adverse effect can be mitigated by increasing the scanning speed to 488 mm/s (Figure 2c).SLM processing using this speed corresponds to sufficient energy density to fully melt the powder particles, avoiding the preferential location of the reinforcement particles along the sample edges.No crack or balling phenomena occur at this optimized speed and the 316L/CeO 2 composite sample shows a very high relative density of 99.9% with rather well-distributed reinforcing particles.
Both the unreinforced 316L matrix and 316L/CeO 2 composite consist of a single-phase austenite structure (Figure 4).The CeO 2 phase cannot be detected in all XRD patterns.This can be due to the melting and dissolution of the CeO 2 phase during SLM or because the small amount of reinforcement is below the detection limit of the instrument.The latter possibility is corroborated by the fact that no diffraction peaks of the CeO 2 phase are detected in the 316L/CeO 2 milled powder.In addition, the CeO 2 particles are visible in the XCT image in Figure 2c, further supporting that the CeO 2 phase is not melted during the process.Because XCT analysis was carried out using a voxel size of 5 µm, which sets the lowest limit for the detection of the second phase, it is surprising to observe the CeO 2 particles considering their small starting size (0.5-1 µm).The CeO 2 particles must, therefore, have been clustered during SLM processing to a size suitable for XCT analysis.This hypothesis is corroborated by the SEM micrographs shown in Figure 5: CeO 2 particles with size in the range of 30-200 µm are indeed formed in the 316L/CeO 2 composite.
Technologies 2018, 6, 25 5 of 10 smaller than the laser spot and to the occurrence of the balling phenomenon [33][34][35][36], where the laser penetration depth is not deep enough to weld the neighboring layers [37].To overcome this problem, the decrease of the laser scanning speed is recommended to achieve higher densification levels in SLM parts [38].Lower scanning speeds, and thus the increase of the laser energy input, create a large melt pool and more powder particles are melted [39].
The scanning speed should be selected carefully in order to provide sufficient energy input capable to create a continuous track of molten liquid and a fully dense surface after solidification.The density of CeO2 (7.65 g/m 3 ) is slightly lower than that of 316L (8 g/m 3 ) [40] and, consequently, the scanning speed should be fast enough to shorten the solidification time without giving the reinforcement particles time for floating on the top of the melt pool [18].Decreasing the scanning speed to 350 mm/s, while keeping the other parameters constant, increases the relative density to 98% (Figure 2b); unfortunately, the CeO2 particles are not homogeneously distributed and are mainly located at the edges of the sample.At such a low scanning speed, a large temperature gradient may exist between the center and the edge of the melt pool [41].This may lead to a higher surface tension at the cooler edge, which may then be accompanied by the outward flow of the CeO2 particles from the hot liquid to the edge of the pool, explaining the behavior observed in Figure 2b.This adverse effect can be mitigated by increasing the scanning speed to 488 mm/s (Figure 2c).SLM processing using this speed corresponds to sufficient energy density to fully melt the powder particles, avoiding the preferential location of the reinforcement particles along the sample edges.No crack or balling phenomena occur at this optimized speed and the 316L/CeO2 composite sample shows a very high relative density of 99.9% with rather well-distributed reinforcing particles.
Both the unreinforced 316L matrix and 316L/CeO2 composite consist of a single-phase austenite structure (Figure 4).The CeO2 phase cannot be detected in all XRD patterns.This can be due to the melting and dissolution of the CeO2 phase during SLM or because the small amount of reinforcement is below the detection limit of the instrument.The latter possibility is corroborated by the fact that no diffraction peaks of the CeO2 phase are detected in the 316L/CeO2 milled powder.In addition, the CeO2 particles are visible in the XCT image in Figure 2c, further supporting that the CeO2 phase is not melted during the process.Because XCT analysis was carried out using a voxel size of 5 µm, which sets the lowest limit for the detection of the second phase, it is surprising to observe the CeO2 particles considering their small starting size (0.5-1 µm).The CeO2 particles must, therefore, have been clustered during SLM processing to a size suitable for XCT analysis.This hypothesis is corroborated by the SEM micrographs shown in Figure 5: CeO2 particles with size in the range of 30-200 µm are indeed formed in the 316L/CeO2 composite.Due to the high cooling rate characterizing materials processing by SLM (10 3 -10 6 K/s), metastable phases and microstructures can be formed [6,9,42].The present unreinforced 316L specimen displays a fine cellular microstructure (Figure 6a,b), in agreement with previous reports on 316L fabricated by SLM [43][44][45].The addition of the CeO2 reinforcement does not affect the formation of the cellular microstructure (Figure 6c-e); however, the CeO2 phase induces significant microstructural refinement and decreases the cell size in the composite material with respect to the unreinforced matrix, as demonstrated by the cell size distributions shown in Figure 6f.Grain refinement occurs at a larger length scale as well.EBSD analysis reveals that the average grain size (calculated over more than 2300 grains) of the unreinforced 316L (45 ± 3 µm) is reduced in the 316L/CeO2 composite to about 25 ± 2 µm (Figure 7).The CeO2 particles are thus effective grain refiners, acting as heterogeneous nucleation sites and hindering the growth of both cells and grains [46].The reduced grain size cannot be attributed to the reduced scanning speed used in the 316L/CeO2 composite with respect to the unreinforced 316L.Slower scanning speed would increase the depth and volume of the molten pool, consequently raising the temperature and increasing the time needed for solidification.This, in turn, would give the grains more time to grow, leading to microstructural coarsening rather than refining, in agreement with the work of Dutta Majumdar et al. [47], who Due to the high cooling rate characterizing materials processing by SLM (10 3 -10 6 K/s), metastable phases and microstructures can be formed [6,8,41].The present unreinforced 316L specimen displays a fine cellular microstructure (Figure 6a,b), in agreement with previous reports on 316L fabricated by SLM [42][43][44].The addition of the CeO 2 reinforcement does not affect the formation of the cellular microstructure (Figure 6c-e); however, the CeO 2 phase induces significant microstructural refinement and decreases the cell size in the composite material with respect to the unreinforced matrix, as demonstrated by the cell size distributions shown in Figure 6f.Due to the high cooling rate characterizing materials processing by SLM (10 3 -10 6 K/s), metastable phases and microstructures can be formed [6,9,42].The present unreinforced 316L specimen displays a fine cellular microstructure (Figure 6a,b), in agreement with previous reports on 316L fabricated by SLM [43][44][45].The addition of the CeO2 reinforcement does not affect the formation of the cellular microstructure (Figure 6c-e); however, the CeO2 phase induces significant microstructural refinement and decreases the cell size in the composite material with respect to the unreinforced matrix, as demonstrated by the cell size distributions shown in Figure 6f.Grain refinement occurs at a larger length scale as well.EBSD analysis reveals that the average grain size (calculated over more than 2300 grains) of the unreinforced 316L (45 ± 3 µm) is reduced in the 316L/CeO2 composite to about 25 ± 2 µm (Figure 7).The CeO2 particles are thus effective grain refiners, acting as heterogeneous nucleation sites and hindering the growth of both cells and grains [46].The reduced grain size cannot be attributed to the reduced scanning speed used in the 316L/CeO2 composite with respect to the unreinforced 316L.Slower scanning speed would increase the depth and volume of the molten pool, consequently raising the temperature and increasing the time needed for solidification.This, in turn, would give the grains more time to grow, leading to microstructural coarsening rather than refining, in agreement with the work of Dutta Majumdar et al. [47], who Grain refinement occurs at a larger length scale as well.EBSD analysis reveals that the average grain size (calculated over more than 2300 grains) of the unreinforced 316L (45 ± 3 µm) is reduced in the 316L/CeO 2 composite to about 25 ± 2 µm (Figure 7).The CeO 2 particles are thus effective grain refiners, acting as heterogeneous nucleation sites and hindering the growth of both cells and grains [45].The reduced grain size cannot be attributed to the reduced scanning speed used in the 316L/CeO 2 composite with respect to the unreinforced 316L.Slower scanning speed would increase the depth and volume of the molten pool, consequently raising the temperature and increasing the time needed for solidification.This, in turn, would give the grains more time to grow, leading to microstructural coarsening rather than refining, in agreement with the work of Dutta Majumdar et al. [46], who observed the decrease of the grain size with increasing scanning speed in 316L steel processed by laser assisted rapid fabrication.The addition of the CeO 2 reinforcement has a significant influence on the yield strength (0.2% offset), which increases from 412 ± 7 MPa for the unreinforced 316L to 485 ± 4 MPa for the 316L/CeO 2 composite while retaining appreciable plastic deformation (Figure 8).The observed increase of strength can be ascribed to the load bearing capacity of the CeO 2 reinforcement [47] along with the Hall-Petch strengthening contribution resulting from structural refinement [48].
observed the decrease of the grain size with increasing scanning speed in 316L steel processed by laser assisted rapid fabrication.The addition of the CeO2 reinforcement has a significant influence on the yield strength (0.2% offset), which increases from 412 ± 7 MPa for the unreinforced 316L to 485 ± 4 MPa for the 316L/CeO2 composite while retaining appreciable plastic deformation (Figure 8).The observed increase of strength can be ascribed to the load bearing capacity of the CeO2 reinforcement [48] along with the Hall-Petch strengthening contribution resulting from structural refinement [49].observed the decrease of the grain size with increasing scanning speed in 316L steel processed by laser assisted rapid fabrication.The addition of the CeO2 reinforcement has a significant influence on the yield strength (0.2% offset), which increases from 412 ± 7 MPa for the unreinforced 316L to 485 ± 4 MPa for the 316L/CeO2 composite while retaining appreciable plastic deformation (Figure 8).The observed increase of strength can be ascribed to the load bearing capacity of the CeO2 reinforcement [48] along with the Hall-Petch strengthening contribution resulting from structural refinement [49].

Conclusions
In summary, we have optimized the SLM processing of 316L/CeO 2 composites in order to achieve highly-dense defect-free specimens.This aim can be achieved without the need to explore the effect of the entire set of experimental parameters.Excellent specimens can be synthesized by carefully adjusting the laser scanning speed, while keeping the other parameters constant.The addition of the CeO 2 phase does not change the phase formation during solidification but it affects the microstructure of the composite, which is considerably refined compared with the unreinforced 316L material.The refined microstructure induces significant strengthening in the composite without deteriorating the plastic deformation.These preliminary results not only indicate that highly-dense 316L/CeO 2 composites with enhanced room-temperature strength can be synthesized by SLM, but also they open the possibility to extend the analysis of their properties to high temperatures, enlarging the possible applications of this type of composites.

Figure 1 .
Figure 1.Powder morphology and particle size distribution for: (a,b) as-atomized pure 316L powder and (c,d) 316L/CeO2 powder mixture ball milled for 2 h.

Figure 1 .
Figure 1.Powder morphology and particle size distribution for: (a,b) as-atomized pure 316L powder and (c,d) 316L/CeO 2 powder mixture ball milled for 2 h.

Figure 2 .
Figure 2. XCT images for: (a) an unreinforced 316L specimen synthesized by SLM with a scanning speed of 688 mm/s, (b) a 316L/CeO2 composite synthesized at 350 mm/s, and (c) a 316L/CeO2 composite synthesized at 488 mm/s.Note that the other processing parameters have been kept constant.The small bright particles in (b) and (c) are CeO2 and the black dots in (b) are porosity.

Figure 3 .
Figure 3. SEM micrographs for: (a) an unreinforced 316L specimen synthesized by SLM at 688 mm/s; (b) a 316L/CeO2 composite synthesized at 688 mm/s; and (c) 316L/CeO2 powder mixture ball milled for 2 h.The bright contrast indicated by red arrows in (b) and the small bright particles adhering to the large 316L particles in (c) are the CeO2 phase.

Figure 2 .
Figure 2. XCT images for: (a) an unreinforced 316L specimen synthesized by SLM with a scanning speed of 688 mm/s, (b) a 316L/CeO 2 composite synthesized at 350 mm/s, and (c) a 316L/CeO 2 composite synthesized at 488 mm/s.Note that the other processing parameters have been kept constant.The small bright particles in (b) and (c) are CeO 2 and the black dots in (b) are porosity.

Figure 2 .
Figure 2. XCT images for: (a) an unreinforced 316L specimen synthesized by SLM with a scanning speed of 688 mm/s, (b) a 316L/CeO2 composite synthesized at 350 mm/s, and (c) a 316L/CeO2 composite synthesized at 488 mm/s.Note that the other processing parameters have been kept constant.The small bright particles in (b) and (c) are CeO2 and the black dots in (b) are porosity.

Figure 3 .
Figure 3. SEM micrographs for: (a) an unreinforced 316L specimen synthesized by SLM at 688 mm/s; (b) a 316L/CeO2 composite synthesized at 688 mm/s; and (c) 316L/CeO2 powder mixture ball milled for 2 h.The bright contrast indicated by red arrows in (b) and the small bright particles adhering to the large 316L particles in (c) are the CeO2 phase.

Figure 3 .
Figure 3. SEM micrographs for: (a) an unreinforced 316L specimen synthesized by SLM at 688 mm/s; (b) a 316L/CeO 2 composite synthesized at 688 mm/s; and (c) 316L/CeO 2 powder mixture ball milled for 2 h.The bright contrast indicated by red arrows in (b) and the small bright particles adhering to the large 316L particles in (c) are the CeO 2 phase.

Figure 5 .
Figure 5. SEM micrographs for the 316L/CeO2 composite synthesized by SLM at 488 mm/s: (a) overview showing the distribution of the CeO2 particles; (b) view at higher magnification revealing that clustering of the CeO2 particles occurs during SLM (see also the inset corresponding to the dashed box in (b)).The red arrows indicate the position of the CeO2 particles.

Figure 6 .
Figure 6.SEM images showing the cellular microstructure formed in (a,b) an unreinforced 316L specimen synthesized by SLM at 688 mm/s and (c-e) a 316L/CeO2 composite synthesized at 488 mm/s; (f) Distribution of the cell size in the unreinforced 316L and 316L/CeO2 composite.

Figure 5 .
Figure 5. SEM micrographs for the 316L/CeO 2 composite synthesized by SLM at 488 mm/s: (a) overview showing the distribution of the CeO 2 particles; (b) view at higher magnification revealing that clustering of the CeO 2 particles occurs during SLM (see also the inset corresponding to the dashed box in (b)).The red arrows indicate the position of the CeO 2 particles.

Technologies 2018, 6 , 25 6 of 10 Figure 5 .
Figure 5. SEM micrographs for the 316L/CeO2 composite synthesized by SLM at 488 mm/s: (a) overview showing the distribution of the CeO2 particles; (b) view at higher magnification revealing that clustering of the CeO2 particles occurs during SLM (see also the inset corresponding to the dashed box in (b)).The red arrows indicate the position of the CeO2 particles.

Figure 6 .
Figure 6.SEM images showing the cellular microstructure formed in (a,b) an unreinforced 316L specimen synthesized by SLM at 688 mm/s and (c-e) a 316L/CeO2 composite synthesized at 488 mm/s; (f) Distribution of the cell size in the unreinforced 316L and 316L/CeO2 composite.

Figure 6 .
Figure 6.SEM images showing the cellular microstructure formed in (a,b) an unreinforced 316L specimen synthesized by SLM at 688 mm/s and (c-e) a 316L/CeO 2 composite synthesized at 488 mm/s; (f) Distribution of the cell size in the unreinforced 316L and 316L/CeO 2 composite.

Figure 7 .
Figure 7. EBSD analysis for: (a,b) an unreinforced SLM 316L specimen synthesized at 688 mm/s and (c,d) a SLM 316L/CeO2 composite processed at 488 mm/s.The small yellow particles in (c) are CeO2.

Figure 8 .
Figure 8. Room-temperature compressive stress-strain curves for the unreinforced SLM 316L specimen synthesized at 688 mm/s and SLM 316L/CeO2 composite processed at 488 mm/s.

Figure 7 .
Figure 7. EBSD analysis for: (a,b) an unreinforced SLM 316L specimen synthesized at 688 mm/s and (c,d) a SLM 316L/CeO 2 composite processed at 488 mm/s.The small yellow particles in (c) are CeO 2 .

Figure 7 .
Figure 7. EBSD analysis for: (a,b) an unreinforced SLM 316L specimen synthesized at 688 mm/s and (c,d) a SLM 316L/CeO2 composite processed at 488 mm/s.The small yellow particles in (c) are CeO2.

Figure 8 .
Figure 8. Room-temperature compressive stress-strain curves for the unreinforced SLM 316L specimen synthesized at 688 mm/s and SLM 316L/CeO2 composite processed at 488 mm/s.

Figure 8 .
Figure 8. Room-temperature compressive stress-strain curves for the unreinforced SLM 316L specimen synthesized at 688 mm/s and SLM 316L/CeO 2 composite processed at 488 mm/s.