3.1. Imaging and Electrical Conductance Measurements
Figure 8 depicts the melt pool width along the deposition length, revealing a monotonic increase with rising preheat temperature. At 25 °C, the melt pool width is at its minimum, averaging 4.7 mm. As the preheat temperature increases, the width expands, reaching its maximum at 800 °C, where the mean value exceeds 6.0 mm.
The observed widening of the melt pool is attributed to the diminishing temperature gradient between the melt pool and the surrounding material at elevated temperatures of the substrate. At lower preheat temperatures, a relatively colder substrate provides an efficient conduction pathway that confines the melt pool. At higher temperatures, this gradient weakens, and the temperature-dependent thermal conductivity decreases, reducing the effectiveness of heat dissipation. Consequently, heat accumulates near the melt pool surface and shifts the liquidus isotherms outward, leading to lateral spreading and an increased melt pool width [
27].
Between 25 °C and 400 °C, the increase in width is moderate. However, beyond 400 °C, the rate of expansion intensifies, particularly between 600 °C and 800 °C. At 600 °C and 800 °C, the melt pool width is 1.14 and 1.33 times greater than at 400 °C, respectively. This suggests the existence of a critical threshold (~400 °C), beyond which the influence of preheating becomes significantly more pronounced, accelerating melt pool expansion. The standard deviation of the melt pool width across different preheat temperatures remains less than 0.11 mm. Notably, the standard deviation decreases slightly at higher temperatures, especially at 600 °C (0.085 mm) and 800 °C (0.086 mm), compared to room temperature (0.11 mm). This reduction suggests that higher preheat temperatures contribute to fewer fluctuations of the melt pool width.
Figure 9 shows the change in electrical conductance observed along the depositions at different substrate preheat temperatures. At lower temperatures, 25 °C to 400 °C, the average conductance remains close to each other, showing only a slight decline from 19.1 mS to 18.4 mS. A significant increase in conductance is observed between 400 °C and 600 °C, where the value jumps to 28.7 mS. The conductance reaches its maximum value of 34.4 mS at 800 °C. This shows that the conductance increases with higher temperatures in the selected range due to a larger cross-sectional contact area in the liquid bridge between the wire and molten metal. The slight decrease in conductance predicted in the range between room temperature and 400 °C is not necessarily caused by any significant change in the processing conditions. The data points in this range are all within the confidence interval of the measurements, such that constant conductance is also likely.
The standard deviation remains relatively low across all temperature conditions, ranging from 0.89 mS to 1.34 mS. The lower standard deviation at higher temperatures (600 °C and 800 °C) indicates a steadier melt pool/steadier metal transfer. Qualitative inspection of side-view image sequences (25 representative images per preheat temperature) provided additional context. At 25 °C, short detachment of the wire from the melt pool and pronounced forward-backward oscillations were observed. At 200 °C and 400 °C, the metal transfer became noticeably steadier, with continuous liquid-bridge and minimal oscillation, consistent with the reduced standard deviation of the conductance and melt-pool width observations. At 800 °C, however, periodic vertical wire motion reappeared, and oxide formation became evident on the bead surface (
Figure 7a), indicating that although the electrical contact was continuous, the thermal environment introduced new sources of disturbance.
The liquid bridge (necking) observed in the experiments describes how the wire deforms as it interacts with the laser beam and melt pool. The length (extension of the liquid bridge) and the width (how much the wire thins compared to its original diameter of 1.14 mm) were analyzed at different preheat temperatures. The results show a clear correlation between the temperature and both the extent of the liquid bridge and the smallest width of the liquid bridge (the thinnest section formed during wire deformation), see
Figure 10. The average length of the liquid bridge decreases as preheat temperature increases. At 25 °C, the liquid bridge extends the most, reaching an average of 1.33 mm. As the temperature increases, the length gradually reduces to 0.78 mm at 800 °C, which is 40% shorter than at 25 °C.
In case no droplet forms to break the liquid bridge, the wire thins as it melts, but the final liquid bridge width increases as the preheat temperature rises. At 25 °C, the wire thins the most, reaching an average of 0.5 mm, 43% of the original width of the wire. The liquid bridge width gradually increases to 0.65 mm as the temperature increases to 800 °C. At 800 °C, the average liquid bridge width is 57% of the original width, meaning the wire retains more of its thickness at high temperatures.
Figure 11 shows the average melt pool width of each preheat temperature along with the predicted values by the GPR model. The predicted result shows that melt pool width increases consistently with temperature, ranging from 4.79 mm at 100 °C to 5.68 mm at 700 °C. At higher preheat temperatures, the melt pool volume becomes larger and reaches higher temperatures due to the increased heat. Previous research has shown that preheating the substrate leads to a slower cooling rate, resulting in a larger melt pool volume. Additionally, as the substrate temperature increases, the molten metal remains in a liquid state longer [
18].
Figure 11b presents the wire’s liquid bridge length and width for the preheat temperatures. Data on length and width of the liquid bridge across various substrate temperatures show an inverse relationship. This pattern shows that as the liquid bridge’s length decreases, the liquid bridge’s width increases, indicating a shift in wire necking at different temperatures.
The predictions show that the liquid bridge’s length decreases as the substrate temperature increases, starting at 1.29 mm at 100 °C and reducing to 0.88 mm at 700 °C. The liquid bridge’s width increases as preheat temperature rises, from 0.51 mm at 100 °C to 0.62 mm at 700 °C.
Initially, as the temperature increases from 100 °C to 300 °C, predicted conductance values decrease slightly. However, a significant rise in conductance was noted at 500 °C and further amplified at 700 °C. This sharp increase reflects increased electrical contact between the wire and the melt pool (
Figure 11c). The influence of preheat temperature on electrical conductance, liquid bridge, and the boundary contour width of the melt pool’s top surface can be directly observed through in-process measurements. Conductance measurement and top-view imaging serve as sensing solutions that do not impose constraints on the mechanical flexibility of the processing head relative to the built geometry. Furthermore, these methods can be integrated into the head to shield them from the harsh interaction zone, which emits smoke and heat radiation.
The capability to collect data at varying sampling rates and through two fundamentally distinct sensing modes, scalar data from conductance measurements and field data from top-view imaging, facilitates sensor fusion. This robust in-process data can be leveraged for the automatic control of heat input. Conversely, side-view monitoring of the liquid bridge is less feasible in a general DED-LB/w processing scenario involving arbitrary geometries. This limitation arises from the constraints imposed by the imaging setup. While side-view monitoring provides valuable insights into the process and offers complementary data to the electrical conductance and melt pool width measurements, its utility for automation purposes during DED-LB/w processing is limited.
3.2. Bead Cross-Section Geometries
Figure 12 shows the relationship between substrate preheat temperature and cross-sectional measurements of deposited beads. The measurements include width, height, penetration depth, and total area (added metal plus penetration area). The width showed an increasing trend with the temperature rise, starting from approximately 4876 μm at 25 °C and peaking at 6192 μm at 800 °C (
Figure 12a). The standard deviations were relatively small, except for the 800 °C point, which suggests that there was more variability at the highest temperature. This is likely due to the presence of oxide (
Figure 7a) around the deposited bead that causes uncertainty in cross-sectional width measurements compared to width measurements from top-view images.
The bead height decreased consistently with preheat temperature, starting at 787 μm and reducing to 668 μm at 800 °C, see
Figure 12b. This inverse relationship shows that higher temperatures lead to a flatter bead profile. The standard deviation was low, indicating consistent height measurements across beads. The penetration depth initially decreased slightly but began increasing significantly at higher temperatures, peaking at 1336 μm for 800 °C (
Figure 12c). The increase at higher temperatures resulted in deeper fusion. The higher variability observed at 600 °C and 800 °C suggests inconsistency in penetration depth, caused by the variation in the position of the deepest penetration point across the bead cross-section, at these temperatures. The total cross-sectional area increased sharply with temperature, from approximately 4.5 × 10
6 μm
2 to 9.1 × 10
6 μm
2 (
Figure 12d). The exponential-like growth in total area highlights the pronounced effect of preheat temperature on metal deposition. The trends suggest that higher temperatures promote metal spreading and deeper fusion. The measured total area became less consistent at elevated temperatures. This variability is likely attributed to the uneven penetration area, which influences the overall cross-sectional area of the bead.
The cross-section width predictions also showed a steady increase from 4906 μm at 100 °C to 5930 μm at 700 °C
Figure 12a. This is consistent with the trend observed in the melt pool top surface boundary contour width. Unlike the width, cross-section height is expected to decrease with temperature, from 774 μm at 100 °C to 690 μm at 700 °C. The most significant increase is observed in penetration depth, which rises dramatically from 532 μm at 100 °C to 1073 μm at 700 °C. Predictions also suggest that as the preheat temperature increased, the higher heat input resulted in a larger melt volume and larger cross-sectional area, which increased fusion in the deposited metal and the substrate. As penetration depth increases, the total area of added material and penetration area increase accordingly. The rate of change in all predicted cross-sectional features became steeper beyond 400 °C, reinforcing the idea that after a critical point, heat input increases. Bead characteristics measurements at higher preheat temperatures have a higher standard deviation, given that they are evaluated manually after solidification and depend on where the cross-section was obtained, making them subject to additional sources of uncertainty.
The in-process results indicate that the process dynamics change significantly at preheating temperatures above 400 °C. Beyond this critical threshold, Joule heating in the wire and melt pool becomes more pronounced (see
Figure 13 showing how the electrical power increases from 400 °C), leading to a substantial rise in heat input. The mechanism behind this change is not trivially explained from the observations made, suggesting further analysis by means of fluid dynamic simulations. This is, however, out of the scope of this study. The practical implications of the observations are, however, that these conditions can be observed from the imaging and conductance measurements and thereby enable process monitoring and automatic control. The results also suggest that to maintain consistent heat and mass transfer, one should avoid a heat accumulation indicated by temperatures above the identified threshold. This can be performed by automatically lowering the heat input either by inter-pass waiting times or by adjusting the input energy through the laser power and travel speed modulation.
While the general thermal trends such as larger melt pools and coarser microstructures with increasing preheat temperature are consistent with previous findings in powder- and arc-based DED systems, the present study reveals a coupling specific to the wire-fed DED-LB/w process. The simultaneous increase in electrical conductance and stabilization of the liquid bridge at elevated substrate temperatures indicates that heat accumulation not only governs the thermal field but also influences mass-transfer stability via changes in electrical and geometric contact between the wire and melt pool. This coupling alters the distribution of Joule heating within the wire-melt region, reinforcing the temperature-dependent expansion of the molten pool and stabilizing metal transfer. Such interaction between heat accumulation and electrical-fluidic dynamics is absent in powder-fed systems, where the feedstock is discontinuous and electrically isolated. Consequently, this study elucidates how substrate preheating in DED-LB/w links heat accumulation to metal-transfer behavior, establishing a distinct interdependence not previously identified in other DED processes.
The post-process observations on the impact of preheat temperature on the melt pool volume and cross-sectional geometries are consistent with the in-process observations, thereby confirming the significant influence of preheat temperature on the deposition process.
It is feasible to establish empirical relationships between the in-process data and the cross-sectional geometries within the specific context of the conducted experiments. However, generalizing such empirical relationships to arbitrary deposition scenarios, different alloys, or varying power density distributions of the laser beam is unlikely to be achievable. To address this limitation, future work could focus on developing physics-informed machine learning models or multi-physics simulations that integrate both thermal and fluid dynamic effects. Such models would enable better generalization across different materials and process configurations by grounding data-driven predictions in fundamental heat transfer and melt pool dynamics. Alternatively, systematic experimental parameter mapping under controlled variations in alloy composition and beam profile could help identify transferable features and scaling laws to extend the applicability of empirical relationships.
3.3. Bead Microstructure and Hardness
Figure 14 shows OM micrographs of as-deposited bead microstructures on substrates with different preheat temperatures. All as-deposited beads mainly exhibit a columnar dendritic structure. The OM images clearly show that the size of these structures changes with the preheat temperature, becoming coarser as the preheat temperature increases. This qualitative observation is confirmed by quantitative measurements of the secondary dendrite arm spacing (SDAS), which progressively increases from approximately 2.5 to 7 µm at higher temperatures (
Figure 15a). The predictions follow the same trend, showing a continued increase at even higher temperatures. This change in SDAS with the preheat temperatures can be explained based on the well-established relationship between the SDAS and cooling, as described in the following equation.
where
is the SDAS,
and
are the material’s constants, and
is the cooling rate. According to Equation (1), a smaller cooling rate leads to a larger SDAS. The cooling rate is determined as the product of solidification velocity (R) and temperature gradient (G). i.e., G × R [
28,
29]. An extensive study by Köhnen et al. [
30], through a simulation coupled with an experiment, showed that increasing the preheat temperature of the substrate before the deposition in the laser-based powder bed fusion (PBF-LB) process reduces both G and R, hence reducing the cooling rate of the melt pool during the solidification, which well-explains the increase in the size of the solidification substructure as the temperature of the substrate increases. The cooling rate in DED-LB/w is typically much slower than in PBF-LB due to the larger heat input and melt volume. However, the same trends in both G and R can be observed.
In addition to the increase in the SDAS, an increase in the substrate’s preheat temperature is also found to coarsen the grain size of the as-deposited bead microstructures.
Figure 16 displays the EBSD inverse pole figure (IPF) colored maps of the microstructures, showing that all beads are primarily composed of columnar grains, and the width gradually increases with the substrate’s preheat temperature. The change in the size of the columnar grain structure is reflected in the gradual increase in the length of the columnar grains, represented by the maximum Feret diameter obtained from the EBSD analysis, as shown in
Figure 15b. The maximum Feret diameter corresponds to the largest chord length across each grain and thus reasonably approximates the grain length in the additively manufactured microstructure. The Gaussian process model results are also depicted alongside the EBSD data, providing predicted values for unseen temperatures. The increase in the average grain size with increasing preheat temperature can also be linked to the decrease in the cooling rate. In solidification processing, it is generally observed that slower cooling rates increase the grain size of the as-solidified alloys, which is also the case for AM processes, as summarized by Murr [
31] and Gorsse [
32]. In AM, according to Zhang et al. [
33], the mechanism of grain refinement caused by increased cooling rate is attributed to higher thermal undercooling, which promotes a higher degree of nucleation. Thus, decreasing the cooling rate by preheating the substrate will reduce the extent of undercooling, hence impeding the nucleation of grains, which ultimately coarsens the grain size. Grain size is well-known as one of the key factors affecting mechanical properties (toughness, fatigue, and yield strength), where the coarsening of the grains generally deteriorates these properties. Thus, from a process control standpoint, it becomes paramount to maintain the preheat temperature below the critical threshold by controlling the interlayer temperature to avoid inhomogeneous grain size throughout the building direction when performing multi-layer deposition.
Apart from forming the γ dendrite, the solidification of Alloy 718 also simultaneously involves a significant Nb microsegregation into the solidifying liquid, which eventually leads to the formation of Nb-rich eutectic secondary phases, i.e., NbC and Laves phase. The Laves phase particles are generally considered detrimental as they can adversely impact the mechanical properties, such as ductility, fracture toughness, tensile strength, and fatigue life, owing to their brittle nature [
34]. The deleterious effect of the Laves phase is reported to be more pronounced in the coarse Laves particles than in the finer ones [
35]. The size of the Laves phase also impacts the dissolution kinetics of the Laves phase during the post-heat treatment, where it takes longer to dissolve the coarser ones [
36]. The size of Nb-rich phases in all samples was then measured using ImageJ software (ImageJ 1.54 g) based on the SEM backscatter electron (BSE) images. Ten images were used for the size and area fraction measurement for each deposited bead condition. The examples of the BSD micrographs of all as-deposited samples used for the measurement are shown in
Figure 17. It can be seen from
Figure 15c that the size of Nb-rich phases, which include both NbC and Laves phase, only slightly increases from 0.9 to 1 μm as the substrate’s preheat temperature increases from 25 to 400 °C. Then, a sharp increase in the size of Nb-rich phases to 1.5 μm occurs when the substrate temperature reaches 800 °C. The reason for this abrupt change in Nb-rich phase size between 600 °C and 800 °C is not yet fully understood. Nonetheless, the general trend of increasing Nb-rich phase size with higher substrate temperatures can also be attributed to the lower cooling rate resulting from the preheating. It has been observed that the dendritic structure becomes coarser as the cooling rate decreases, based on the increase in the measured SDAS with increasing substrate temperature. Hence, as solidification progresses, the residual liquid gets confined within these coarser dendritic structures. Consequently, this leads to the formation of course NbC and Laves phase particles. The increased size of the Laves phase in the bead deposited on the hotter substrate may also require careful consideration during the DED-LB/w of Alloy 718, especially if the interlayer temperature is not strictly controlled and exceeds 800 °C, since it may form an even coarser Laves phase and potentially deteriorate the mechanical properties.
The formation of these Nb-rich phases in the interdendritic region due to Nb microsegregation also typically results in the dendrite core composition being depleted in Nb, which is the essential element to form the γ″ phase during the post-age hardening treatment. The amount of the Nb-rich secondary phases is one of the parameters that can be used to scale the extent of Nb microsegregation during the solidification of Alloy 718 [
36,
37]. A larger area fraction of the phases could indicate a higher degree of microsegregation. In general, it is believed that a higher cooling rate during solidification would result in lower Nb microsegregation and, hence, a lower fraction of Nb-rich phases, as reported by Radhakrishna and Rao [
37] through experiments and Kumara et al. [
38] through phase field modeling. However, it was observed that the area fraction of the Nb-rich phases did not change notably as the substrate preheat temperature increased (
Figure 15c). Note that although the area fraction of the phases in the beads that were deposited on the preheated substrate seems to be marginally lower compared to the one that was not preheated; nevertheless, considering the standard deviations that considerably overlap, the area fraction of the Nb-rich phases is arguably comparable across all samples.
To explain the similarity of the Nb-rich phase area fraction in all samples, the partition coefficient of Nb during solidification was assessed. The partition coefficient of a particular alloying element is an important solidification parameter that describes the extent of elemental microsegregation during solidification. The solidification follows the non-equilibrium mode at a rapid cooling rate, such as in AM processes. In this condition, the back diffusion is assumed to be negligible, and hence, the solute partitioning behavior into the interdendritic liquid is often approximated to follow the Scheil solidification equation.
Here,
Cs is the concentration of a particular element in the solidified solid or dendrite,
C0 is the alloy’s chemical composition,
fs is the solid fraction, and k is the partition coefficient of the element. At the beginning of solidification (
fs = 0), supposing local equilibrium conditions and negligible undercooling at the dendrite tips, the first solid phase to form from the liquid, the dendrite core will contain a composition of
kC0. Consequently, the ratio between the dendrite core’s composition and the alloy’s nominal composition gives the initial
k value at the onset of solidification. It is worth noting that the
k value is not necessarily unchanging throughout the solidification. It, however, still provides valuable insight into the extent of microsegregation of alloying elements. The k value lower than unity shows that the element tends to partition or be rejected into the interdendritic liquid during solidification, whereas the value higher than unity suggests a preferential partitioning into the dendrite. The average concentrations of Nb in the dendrite core in all samples determined by SEM-EDS analysis on 15 points at the dendrite core’s center and the corresponding kNb value are listed in
Table 3. It is shown that kNb values are much less than unity and comparable across all samples with different substrates preheat temperatures, suggesting that the extent of microsegregation of Nb into the liquid in all samples is similar. The comparable k values of Nb could explain the similarities in the Nb-rich phase area fraction across all samples with different substrates’ preheat temperatures.
The nearly constant
k values observed, regardless of substrate temperature (and thus the cooling rate), did not follow the general understanding of partitionless solidification in rapid solidification [
39]. According to this concept, increasing the cooling rate may lead to higher concentrations of Nb in the dendrite core (thus, a larger kNb value), bringing it closer to the alloy’s bulk composition since the solutes are trapped at the moving solid/liquid interface due to their incomplete partitioning. Zhang et al. [
40] found that the dendrite core in PBF-LB-built Alloy 718 contained the highest Nb concentration, followed by the DED-LB/p and cast counterparts, respectively. The PBF-LB typically results in the fastest cooling rates during solidification, while casting is the slowest. However, it should be noted that these three processes fundamentally differ, resulting in significantly different cooling rates. In this study, even though increasing the substrate temperature before deposition reduces the cooling rate, the process remains DED-LB/w with the same process parameters, which could not be as substantial as the difference in cooling rate due to entirely different processes, e.g., PBF-LB and DED-LB/p or DED-LB and cast. To estimate the cooling rate during solidification of Alloy 718 by PBF-LB, DED-LB/p, and cast, based on the study by Zhang et al. [
40], Equation (1) was used. The SDAS of PBF-LB-built Alloy 718 reported by Zhang et al. [
39] was at least one order and two orders of magnitude finer than the DED-LB/p built and cast counterparts, respectively. Using
and
of 62.9 and 0.407, respectively, for Alloy 718 [
41], the corresponding cooling rates were estimated to differ by approximately two orders of magnitude between the PBF-LB-built and DED-LB/p-built materials, and similarly between the DED-LB/p-built and cast conditions. In contrast, the predicted cooling rates for beads deposited on substrates at 25 °C and 800 °C, based on the measured SDAS values, are approximately 3100 °C/s and 220 °C/s, respectively, representing only about one order of magnitude difference. This significantly smaller difference in cooling rate within the DED-LB/w process in comparison to the cooling rate difference among distinct manufacturing routes, i.e., PBF-LB-built and DED-LB/p, cast, supports the observation that the kNb and Nb-rich phase fraction remain nearly constant despite changes in substrate temperature. As a result, the reduction in cooling rate due to the higher preheat substrate temperatures could not be significant enough to increase the kNb value relative to decreasing the cooling rate by changing the process from PBF-LB to DED-LB/p or DED-LB/p to cast.
It is acknowledged that the highest substrate preheat temperature used in this study (800 °C) exceeds the range typically encountered during multi-layer DED-LB/w, where interlayer temperatures are generally below 600 °C. The inclusion of this extreme condition was deliberate: it was selected to establish the upper bound of thermal exposure and to examine the onset of microstructural degradation mechanisms such as coarsening of Laves phases and grain growth. By extending the preheating range to 800 °C, the experiment captured the transition from beneficial thermal moderation, reducing residual stresses and promoting melt pool stability, to detrimental overheating, where the solidification substructure and Nb-rich phase morphology degrade. In this sense, the 800 °C data does not represent a recommended processing condition but rather defines the process limit beyond which Alloy 718’s microstructural integrity and mechanical performance begin to deteriorate. This boundary is essential for guiding practical process control, as it quantifies the temperature threshold that should not be exceeded to maintain the alloy’s high-performance characteristics.
The hardness of all as-deposited beads with different substrate preheat temperatures revealed no significant difference in the average hardness across all samples, which are about 250 HV and 260 HV. The hardness of the as-deposited beads is very similar to that reported by Segerstark et al. [
42] in their work on DED-LB/p-built Alloy 718. The similar hardness values can be explained by the comparable area fraction of Nb-rich phases, especially the Laves phase, across all the samples, since the Laves phase is a hard-brittle intermetallic constituent that can contribute to the average hardness of the sample. In addition, no evidence of hardening phases, i.e., γ′ and γ″, is found in all samples in the dendrite core or interdendritic region (
Figure 18). Since the indentation diagonal in all samples was about 45 μm, which covers both dendritic core areas and interdendritic regions, the absence of both hardening phases in both regions further explains the similarity in hardness across all as-deposited beads. JMatPro simulation was carried out to calculate the CCT diagram of Alloy 718 based on the composition in the dendrite core and the interdendritic region. The compositions of these two regions were determined by SEM-EDS analysis. The CCT diagram (
Figure 19) shows that even at a cooling rate of 1 °C/s, it does not touch the noses of γ′ and γ″ precipitation. The cooling rate during the DED-LB/w process with different substrate preheating temperatures is estimated to be in the range of 200–3000 °C/s (between the cooling rate of DED-LB/p and casting), which explains the absence of the hardening phases in both regions.
The observations regarding the impact of preheat temperature on the resulting microstructure indicate that heat accumulation in DED-LB/w presents a challenge that must be mitigated through various heat input control strategies. These strategies are essential to ensure the structural integrity of as-built AM components and to minimize the need for time- and energy-intensive post-heat treatments.