Additive manufacturing (AM) fabricates complex geometries inaccessible through other manufacturing techniques. However, each AM platform imposes unique process-induced constraints which are not addressed by traditional polymeric materials. Vat photopolymerization (VP) represents a leading AM platform which yields high geometric resolution, surface finish, and isotropic mechanical properties. However, this process requires low viscosity (<20 Pa·s) photocurable liquids, which generally restricts the molecular weight of suitable VP precursors. This obstacle, in concert with the inability to polymerize high molecular weight polymers in the printer vat, effectively limits the molecular weight of linear network strands between crosslink points (Mc) and diminishes the mechanical and elastic performance of VP printed objects. Polymer colloids (latex) effectively decouple the relationship between viscosity and molecular weight by sequestering large polymer chains within discrete, non-continuous particles dispersed in water, thereby mitigating long-range entanglements throughout the colloid. Incorporation of photocrosslinking chemistry into the continuous, aqueous phase of latex combined photocurability with the rheological advantages of latex and yielded a high molecular weight precursor suitable for VP. Continuous-phase photocrosslinking generated a hydrogel scaffold network which surrounded the particles and yielded a solid "green body" structure. Photorheology elucidated rapid photocuring behavior and tunable green body storage moduli based on scaffold composition. Subsequent water removal and annealing promoted particle coalescence by penetration through the scaffold, demonstrating a novel approach to semiinterpenetrating network (sIPN) formation. The sIPN's retained the geometric shape of the photocured green body yet exhibited mechanical properties dominated by the high molecular weight latex polymer. Dynamic mechanical analysis (DMA) revealed shifting of the latex polymer and photocrosslinked scaffold T_g's to a common value, a well-established phenomenon due phasemixing in (s)IPN's. Tensile analysis confirmed elastic behavior and ultimate strains above 500% for printed styrene-butadiene rubber (SBR) latexes which confirmed the efficacy of this approach to print high performance elastomers. Further investigations probed the versatility of this approach to other polymer compositions and a broader range of latex thermal properties. Semibatch emulsion polymerization generated a systematic series of random copolymer latexes with varied compositional ratios of hexyl methacrylate (HMA) and methyl methacrylate (MMA), and thus established a platform for investigating the effect of latex particle thermal properties on this newly discovered latex photoprocessing approach. Incorporation of scaffold monomer, N-vinyl pyrrolidone (NVP), and crosslinker, N,N'-methylene bisacrylamide (MBAm), into the continuous, aqueous phase of each latex afforded tunable photocurability. Photorheology revealed higher storage moduli for green bodies embedded with glassy latex particles, suggesting a reinforcing effect. Post-cure processing elucidated the necessity to anneal the green bodies above the T_g of the polymer particles to promote flow and particle coalescence, which was evidenced by an optical transition from opaque to transparent upon loss of the light-scattering particle domains. Differential scanning calorimetry (DSC) provided a comparison of the thermal properties of each neat latex polymer with the corresponding sIPN. Another direction investigated the modularity of this approach to 3D print mixtures of dissimilar particles (hybrid colloids). Polymer-inorganic hybrid colloids containing SBR and silica nanoparticles provided a highly tunable route to printing elastomeric nanocomposite sIPN's. The bimodal particle size distribution introduced by the mixture of SBR (150 nm) and silica (12 nm) nanoparticles enabled tuning of colloid behavior to introduce yield-stress behavior at high particle concentrations. High-silica hybrid colloids therefore exhibited both a shear-induced reversible liquid-solid transition (indicated by a modulus crossover) and irreversible photocrosslinking, which established a unique processing window for UV-assisted direct ink write (UV-DIW) AM. Concentric cylinder rheology probed the yield-stress behavior of hybrid colloids at high particle concentrations which facilitated both the extrusion of these materials through the UV-DIW nozzle and the retention of their as-deposited shaped during printing. Photorheology confirmed rapid photocuring of all hybrid colloids to yield increased moduli capable of supporting subsequent layers. Scanning electron microscopy (SEM) confirmed well-dispersed silica aggregates in the nanocomposite sIPN's. DMA and tensile confirmed significant reinforcement of (thermo)mechanical properties as a result of silica incorporation. sIPN's with relative weight ratio of 30:70 silica:SBR achieved maximum strains above 300% and maximum strengths over 10 MPa. In a different approach to enhancing VP part mechanical properties, thiol-ene chemistry provided simultaneous linear chain extension and crosslinking in oligomeric diacrylate systems, providing tunable increases to Mc of the photocured networks. Hydrogenated polybutadiene diacrylate (HPBDA) oligomers provided the first example of hydrocarbon elastomer photopolymers for VP. 1,6-hexanedithiol provided a miscible dithiol chain extender which introduced linear thiol-ene chain extension to compete with acrylate crosslinking. DMA and tensile confirmed a decrease in T_g and increased strain-at-break with decreased crosslink density. Other work investigated the synthesis and characterization of first-ever phosphonium polyzwitterions. Free radical polymerization synthesized air-stable triarylphosphine-containing polymers and random copolymers from the monomer 4-(diphenylphosphino) styrene (DPPS). ³¹P NMR spectroscopy confirmed quantitative post-polymerization alkylation of pendant triarylphosphines to yield phosphonium ionomers and polyzwitterions. Systematic comparison of neutral, ionomer, and polyzwitterions elucidated significant (thermo)mechanical reinforcement by interactions between large phosphonium sulfobetaine dipoles. Broadband dielectric spectroscopy (BDS) confirmed the presence of these dipoles through significant increases in static dielectric content. Small-angle X-ray scattering (SAX) illustrated ionic domain formation for all charged polymers. / Doctor of Philosophy / Additive manufacturing (AM) revolutionizes the fabrication of complex geometries, however the utility of these 3D objects for real world applications remains hindered by characteristically poor mechanical properties. As a primary example, many AM process restrict the maximum viscosity of suitable materials which limits their molecular weight and mechanical properties. This dissertation encompasses the design of new photopolymers to circumvent this restriction and enhance the mechanical performance of printed materials, with an emphasis on elastomers. Primarily, my work investigated the use of latex polymer colloids, polymer particles dispersed in water, as a novel route to provide high molecular weight polymers necessary for elastic properties in a low viscosity, liquid form. The addition of photoreactive molecules into the aqueous phase of latex introduces the necessary photocurability for vat photopolymerization (VP) AM. Photocuring in the printer fabricates a three-dimensional object which comprises a hydrogel embedded with polymer particles. Upon drying, these particles coalesce by penetrating through the hydrogel scaffold without disrupting the printed shape and provide mechanical properties comparable with the high molecular weight latex polymer. As a result, this work introduces high molecular weight, high performance polymers to VP and reimagines latex applications beyond 2D coatings. Further investigations demonstrate the versatility of this approach beyond elastomers with successful implementations with glassy polymers and inorganic (silica) particles which yield nanocomposites.

Research interest in Additive Manufacturing (AM) as an enabling technology for customizable parts is rapidly expanding. While much AM research focus is on high performance feedstocks and process optimization to obtain parts with improved mechanical properties, interest in the environmental applications of AM has recently increased. The lower cost and greater accessibility AM is leading to novel environmental research solutions in wastewater treatment and toxicity reduction by capitalizing on the increased affordability and accessibility of 3D printing (3DP) technologies for customizable, high surface area structures. The novelty and focus of this dissertation is exploration of Material Extrusion (MatEx) based Fused Filament Fabrication (FFF) of filled polymer composites as a disruptive technology enabler for deployable and retrievable structures in environmental media for adsorption, destruction and toxicity reduction of harmful chemicals. This dissertation addresses research questions that generally answer, "why AM for environmental applications?". The inherent layer-by-layer design provides larger surface area structures for interaction with contaminated media. Polylactic acid (PLA) was selected due to its green sources and biocompatibility relative to synthetic polymers and its wide processing window allowing shear thinning and "printability" despite the elevated viscosity and modulus of highly filled composites. The filler selected for contaminant adsorption was microporous zeolite, which has affinity for ammonia, radionuclides and Per- and Polyfluorinated Substances (PFAS). The filler selected for contaminant destruction was photocatalytic TiO2 nanoparticles which can degrade organic chemicals, harmful algal bloom toxins and PFAS. A preliminary research hurdle was overcome by demonstrating that immobilization of zeolite and TiO2 in a PLA binder matrix did not prevent adsorption or free radical release, respectively. The first major research objective involved investigation of high surface area printed PLA-zeolite geometries with different zeolite loadings and found that while ammonia was reduced, there were diminishing returns with increased loading in terms of mass standardized adsorptive performance due to insufficiently exposed zeolite. The research solution leveraged AM print process parameters to increase the macroporosity of the printed composite structure to create voids and channels allowing water infiltration and chemical adsorption to zeolite. Faster printing of larger roadways generated macrostructural voids that were maintained by extrusion at lower temperature for rapid solidification. The second research objective involved compounding different loadings and dispersion states of TiO2 in PLA to demonstrate immobilization of TiO2 closer to UV-light penetration water improves photocatalysis. Higher 32% w/w TiO2 loadings were heavily agglomerated and more difficult to print process due to high viscosity, rapid liquid-solid transition (G'>G") and particle network recovery during printer retractions, leading to nozzle clogging. Lower 20% w/w loading was more conducive to larger production printing due to lower viscosity, longer viscosity recovery times for retractions and thus generally a wider processing window. While altering twin screw processing parameters reduced TiO2 agglomerates in filaments, leading to increases in crystallinity (due to seeding effects and chain scission) and lower viscosity recovery, photocatalytic performance was not significantly improved. Evidence presented showed that larger particle agglomerates were more toward the inside of printed surfaces and thus less available to UV-light irradiation. This location of larger particles is supported by previous theoretical and empirical investigations showing larger particles migrate at a faster velocity away from the outer walls of confined extrudates within non-Newtonian flow fields due to normal forces, leaving more smaller particles toward outer surfaces. This research provided novel contributions to the environmental and AM research communities and pioneered a convergence of these fields into an interdisciplinary community of practice focused on better characterization and processing in environmental applications to improve structure-environmental property relationships. Future research should build on these findings to enhance performance through multi-functional materials that adsorb and destroy contaminants. The reactive surface area should be further increased through by high surface area designs and print parameter optimized porous structures providing a continuum of meso- to microporosity as confirmed by chemical flux and mass transfer studies for additional AM technologies (e.g., Direct Ink Write). / Doctor of Philosophy / Engineers and hobbies alike have great interest in Additive Manufacturing (AM), or 3D Printing, to customize parts and new designs. More recently, environmental scientists and engineers have turned to 3D printing to solve environmental problems due to the lower cost and user-friendliness of desktop machines. This research dissertation focuses on how 3D printing can allow for iterative improvements in customizable, high surface area structures to reduce chemical concentrations in water by either adsorbing or destroying the chemicals. Water is clearly a critical resource for ecosystems, recreation and drinking supplies as national security, human and ecosystem health are tied to clean water. This research addresses why 3D printing is interesting and effective for environmental solutions. Briefly the layer-by-layer design provides larger surface area structures for interaction with contaminated media. The common 3D printer feedstock Polylactic Acid (PLA) was selected since it is non-toxic and can be relatively easy to print even if modified by adding rigid filler particles for research. Micron-scale (zeolite) and nano-scale (Titanium Dioxide) particles were mixed with the polymer to make printable filaments to adsorb and destroy contaminants, respectively. This research demonstrated the proof-of-concept by removing ammonia, methylene blue dye and a harmful algal toxin from water. The materials produced are also applicable to both conventional organic pollutants and emerging contaminants of concern in the popular news such as Per- and Polyfluorinated Substances (PFAS), which were used as flame retardants and non-stick surfaces. This research ties the material properties of the experimental micro- and nano-composite filaments to how the materials extrude and solidify during 3D printing and how well the resulting printed structures work for reducing contaminant levels in water. Altering the parameters and conditions at which these materials are processed and 3D printed can significantly change their structure, density, porosity and distribution of particles and in turn increase effectiveness. The results provide new contributions to both the environmental and AM research communities and pioneers interdisciplinary collaborative ideas for these different subject matter experts to work together to better understand how handling and processing of these materials can improve their performance in environmental applications. New work should leverage the ideas and principles presented here to further improve performance, ease of production and scale-up of multifunctional material structures for multiple classes of chemicals that are of concern in surface and drinking water.

Binder jetting is an additive manufacturing process that layer by layer builds a 3D model by selectively binding regions of powder using binder deposited though an inkjet printhead. The process offers several advantages over other additive manufacturing processes including fast build rates, vast material selection, decreased cost, and part resolution. The main disadvantage of binder jetting is poor mechanical properties, stemming from a poor understanding of the process physics. Porosity in final parts is not uncommon, but there is little understanding of where the porosity originates. The purpose of this thesis is to report the investigation of increased powder bed cohesion and its effects on part formation, part properties, and printing parameters in binder jetting. The interaction between binder and powder is complex. Binder exiting the printhead impacts the powder bed at speeds up to 10 m/s. The kinetic energy carried by the droplet disperses into the powder bed on impact, causing some powder particles to eject from the bed and other particles to rearrange within the bed. The particle ejection and rearrangement is theorized to be the physical cause of porous regions in binder jetted parts. This work uses a method called pre-wetting to introduce small amounts of moisture into the powder bed to effectively increase the cohesive forces between powder particles. Increased cohesion makes particle ejection and rearrangement during the powder/binder interaction more difficult. A method of accomplishing pre-wetting was developed and achieved successful moisture delivery using water and a water/tri-ethylene glycol mixture. Printed lines were used to characterize moisture content and study its effects on line formation and saturation levels. Low levels of moisture were shown to perform the best. Particle ejection and rearrangement was shown to decrease with moisture addition. Pre-wetting was shown to eliminate the defect known as balling, increasing the parameters known to successfully print lines. Water was identified as a poor substance for pre-wetting due to rapid evaporation, but tri-ethylene glycol/water solutions succeeded in proper moisture delivery. Saturation levels in lines decrease with added moisture and part dimensions increase. high-speed x-ray imaging verified pre-wetting reduction in particle ejection and rearrangement as well as supply some preliminary understanding of void formation during the printing process. The first few layers of the binder jetting process have been shown to increase in surface roughness values when compared to the undisturbed powder bed. This is likely due to a balling-like effect seen in layers. The effects of pre-wetting on layer and multi-layer formation were studied. Pre-wetting reduced the surface roughness levels in printed layers to the levels near the levels seen in undisturbed powder beds. In contrast, saturation levels in layers and multi-layers increased in value above those found in parts printed into dry powder, giving indication that porous regions within bound parts are being eliminated. Layer and multi-layer parts showed increased part dimensions with the addition of moisture. Overall, pre-wetting was shown to greatly reduce the effects of the binder/powder interaction and results strongly suggest that pre-wetting mitigates defect creation during the printing process. Further research should include testing of thicker multi-layer parts to study how saturation trends continue with increased layer numbers. In-process drying should be used in conjunction with pre-wetting in multi-layer parts to determine its effects on saturation levels and part dimensions. Post processing should be done to partially sinter, or infiltrate multi-layer parts created with and without pre-wetting to analyze porosity.

Master of Science / Material extrusion is a common form of 3D printing that has historically been limited to producing prototypes, models, and low load-bearing parts. This is primarily because parts are manufactured layer-by-layer, resulting in poor adhesion along the build direction, and machines struggle to print with high-strength polymers, which tend to shrink significantly as they cool. However, one way to address these limitations is to use fiber-reinforced materials in combination with multi-axis deposition strategies. In material extrusion, embedded fibers will align themselves along the deposition path, providing structural, thermal, and chemical improvements. Multi-axis toolpathing can enable the deposition of this fiber-filled material in full 3D along a part's expected stress paths. This is possible using a complex kinematic system like an industrial robot arm that can rotate the angle of the tool relative to the part as it is printing. The objective of this work was to develop and test a tool capable of multi-axis continuous carbon fiber reinforcement, which required a dedicated cutting mechanism to shear the fiber at the end of each deposition path, control over the amount of fiber used, and a slender tool profile to avoid collisions during multi-axis printing. The findings of this work revealed that while the use of continuous carbon fiber further reduced the adhesion between deposition paths, it substantially improved the strength of the part along them. To validate the multi-axis capability of the system, a toolpath was generated for a curved tensile bar. The results showed that the continuous carbon fiber multi-axis toolpath resisted a load 820.57% higher than an XY-planar sliced part printed with traditional filament, confirming the effectiveness of the presented approach. Multi-axis motion can also be used for avoiding support material requirements. In traditional 3-axis material extrusion, steep overhanging features often require additional, sacrificial material to be printed underneath. This leads to longer print times, more material waste, and a poor surface finish left behind on the final part. To minimize the amount of support material required, various techniques have been explored, including changing the toolpath, part geometry, or material processing parameters. However, none of these techniques have been successful in eliminating the need for supports entirely. A promising approach to address this issue is multi-axis material extrusion, where the angle of the printing tool and the direction of the layers can be precisely controlled during the printing process. This technique can be used to ensure that the tool is always extruding material onto a well-supported surface, rather than over thin air. However, research to date has not yet fully explored how the range of achievable overhang features changes as the tool is rotated. To address this knowledge gap, this work used an industrial robot arm equipped for material extrusion to investigate the relationship between tool angle, build direction, and achievable overhang threshold. The results showed that the same overhang limitations that exist in the XY plane will rotate with the tool and are unaffected by gravitational forces. These findings provide valuable insights for advancing the use of multi-axis material extrusion in the production of complex and intricate 3D objects without the need of supports.

Doctor of Philosophy / Startups can and do fail. For an entrepreneur, product developer, or researcher with a physical and capital-intensive product idea, this dissertation can serve as a resource to bridge the gaps between business, engineering, and design and reduce the risk of failure when trying to create a startup. The process described in this dissertation describes how to evaluate the key elements of an idea and conduct a series of interviews with potential customers to find evidence that supports pursing that idea further, challenge the startup team to change some aspect of the idea, or drop it altogether. Once the startup team has found a problem, as well as a solution to that problem, this dissertation describes an approach creating that solution. Then this dissertation describes an approach for critically evaluating the foundational elements of the problem and the solution. The goal for a critical evaluation is to identify additional foundational elements which relate to the product that may increase its value or decrease the risk of product failure.

Pure copper is widely employed as the primary metal in thermal management and electromagnetic applications due to its exceptional electrical and thermal conductivity. Laser powder bed fusion (LPBF) is a versatile additive manufacturing technique that utilizes high laser energy to selectively melt and fuse successive layers of metal powder to create metallic components with intricate geometries. Nonetheless, LPBF of pure copper is known as a challenging manufacturing process attributed to low optical absorptivity, rapid dissipation of laser energy, and affinity to oxidation. This thesis focuses on the process development and optimization for LPBF of Cu. Firstly, the Process-structure-property relation was examined by assigning a wide range of process parameters to print Cu-LPBF coupons. The optimum process parameters were defined based on maximum relative density, which was obtained at the full laser power of the EOS M280. The results emphasized the significant impact of laser power and hatch spacing on the part quality. Second, Cu oxide exhibits higher optical absorption than pure copper, as reported in the literature. Therefore, the thin film of oxide that was created either on recycled or intentionally oxidized power particles would be a possible easy way to increase the heat energy absorbed from the laser beam. However, the current work emphasized the adverse effects of oxide presence on part quality, particularly when using a medium laser power machine. In this regard, a new method of in-situ Cu oxide reduction during LPBF was proposed to develop an easy and environment-friendly approach to recover the contaminated powder. Applying laser ablation on the powder surface and the solidified layers results in considerable improvement, where the oxygen content is reduced by 70% in the LPBF samples compared to the initial state of the oxidized powder. Finally, the power density of Cu-LPBF coils was improved by enhancing the filling factor and increasing the electrical conductivity. The dimensional limitation of Cu-LPBF fabricated parts was initially identified. The power of utilizing sample contouring was highlighted to upgrade surface quality. Adjusting beam offset associated with optimum scan track morphology upgraded the minimum feature spacing to 80 um. The electrical impedance of full-size Cu-LPBF coils, newly reported in this study, was measured and compared with solid wire. It can reflect the performance of Cu-LPBF coils (power factor) in high-frequency applications. / Thesis / Doctor of Philosophy (PhD)

Ceramic colloidal processing routes such as slip casting, gelcasting and direct ink writing provide valuable insight into the role of interaction forces between particles, solvents, and polymeric additives in the rheology, particle packing, and strength of a ceramic green body. For difficult-to-densify ceramics such as the UHTCs, which find their place in extreme environment applications, precise control of each step of the manufacturing process is key. In this work, a fundamental study on the interaction between particles in non-aqueous slip casting is performed comparing the rheological behavior and consolidation with current models for interaction potential within a suspension. The advantages and drawbacks of such a model are discussed in relation to formulating a colloidal process for advanced ceramics such as ZrB2, and a case for a cyclohexane slip casting system resulting in low viscosity, shear-thinning behavior and green density of 64%, is made. The focus on non-aqueous colloidal processing is extended to gelcasting, involving three different sets of chemically curable polymer systems: HEMA+MBAM, TMPTA, and PEGDA. Merits of the gelcasting process including homogeneity, green strength, and processing time reduction are discussed, with the HEMA+MBAM system resulting in nearly an order of magnitude increase in green density from slip casting. Gelcast samples were also sintered to a density of 88% and capable of being processed in a variety of complex shapes with fine feature size on the mm scale. The properties examined in slip casting and gelcasting, as well as others pertaining to the setup of an extrusion-based additive manufacturing system, are carefully considered to design an ink that has been used to print ZrB2. The role of each additive as well as the solvent in creating an ink that is not only within the correct viscosity range for extrusion and shape retention, but also produces a strong and densely packed green body, is discussed. Finally, adjustment of printing parameters, and the method of using a low-cost rheology match to tune the settings of a pneumatic screw-extrusion printing setup, are explained. Each of these processes points to new and practical methods of complex shaping ZrB2 that can provide insight into processing of these challenging materials and create new avenues for their use in extreme environment applications, such as thermal protection systems in atmospheric re-entry vehicles. / Doctor of Philosophy / This work examines the use of ultra-high temperature ceramics (UHTCs), which are materials with some of the highest melting points in existence. These are an intriguing option for extreme environment applications. One such application is the protection of rockets, scramjets, and other hypersonic (speed > Mach 5) vehicles from the high temperatures experienced during flight and re-entry. In this work, the UHTC Zirconium diboride (ZrB2) is used as a reference material. For many of the same reasons UHTCs such as ZrB2 have extreme melting points, they can be difficult to manufacture, particularly in complex shapes. Like many ceramics, UHTCs are not melted and cast as metals are, but rather are processed in powder form to a compact known as a green body. The green body is placed in a high-temperature furnace at 2/3 - 3/4 of the melting point, where the powder undergoes sintering, or consolidation into a dense part. The manufacture of a green body that is versatile in its capacity to be molded into any shape, and allows for close packing of the particles in the powder compact to avoid failure-inducing flaws in the final component under intense loads, remains a challenge for UHTCs. Most UHTCs are hot pressed, where the powder alone is consolidated under intense heat and pressure, but this process offers very little complex shaping capacity or control of the uniformity of the part. In this work, three methods for green body manufacture using colloid-based routes, which all have unique capabilities and challenges, are described. The first process is slip casting, which is a centuries-old process that has been used for the manufacture of pottery, whitewares, and art ceramics. When used effectively, slip casting ensures that the forces between ceramic particles in a suspension, or "slip", are well-controlled such that the ceramic particles will not form clumps, or agglomerates, which create non-uniformities that weaken the final component. With information about the powder, solvent, and additives in a slip, the extent to which this will be effective can be predicted with mathematical models. This work compares the results of these models with slip casting suspensions in different solvent environments to gain knowledge about slip casting as an option for complex shaping of ZrB2. The second colloidal process discussed is gelcasting, in which the suspension of ceramic powder can undergo chemical gelation, or a reaction that transitions the suspension from a liquid to a solid, not unlike that of a natural gel such as gelatin, agarose, or albumin (egg white). The gel, which is loaded with ceramic powder, allows for more versatile shaping than slip casting, and shorter processing time; a gelcast ceramic is generally solidified in less than an hour, while a slip cast typically dries overnight. The presence the gel also provides strength to the green body, which is advantageous in handling as well as any machining to adjust the shape that may be necessary prior to sintering. The final process detailed in this work is direct ink writing, a type of additive manufacturing (or 3D printing). Knowledge gained from slip casting and gelcasting was used to carefully design a ceramic colloid that could be deposited in a layer-by-layer fashion to create a complex shape with high uniformity and control, as well as minimal surface cracking. The printed green bodies were compared in strength and sintering behavior to the gelcasts from previous chapters, and the expansion of shaping capacity for each route as it relates to aerospace applications, is described.

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To analyze the impact of different objective functions and additive manufacturing (AM)constraints on structural topology optimization, it is necessary to perform an in-depth comparative study. This analysis should consider specific structural design factors, such as compliance, volume, or stress minimization, and assess their effects on the topology optimization for AM. In addition, the inclusion of AM constraints can have a significant influence on various aspects, including optimal part geometry, part volume, support structure volume, and structural performance. Thus, it is essential to examine and compare these factors to determine the optimal part design for AM. This study focuses on comparing topology optimization results obtained using compliance, stress, or multi-objective minimization, with and without AM constraints. The comparative analysis is conducted in the study, utilizing four structural design examples: cantilever beam, bridge-shaped structure, L-shaped beam and connecting rod. The comparison results provide insights into the effects of build orientation, AM constraints such as overhang, and different design objectives on the structural topology optimization for AM

Thermoelectric generators convert heat energy to electricity and can be used for waste heat recovery, enabling sustainable development. Selective Laser Melting (SLM) based additive manufacturing process is a scalable and flexible method that has shown promising results in manufacturing high ZT Bi2T e3 material and is possible to be extended to other material classes such as M g2Si. The physical phenomena of melting and solidification were investi- gated for SLM-based manufacturing of thermoelectric (M g2Si) powders through comprehen- sive numerical models developed in MATLAB. In this study, Computational Fluid Dynamics (CFD)-based techniques were employed to solve conservation equations, enabling a detailed understanding of thermofluid dynamics, including the temperature evolution and the con- vection currents of the liquid melt within the molten pool. This approach was critical for optimizing processing parameters in our investigation, which were also used for printing the M g2Si powders using SLM. Additionally, a phase field-based model was developed to sim- ulate the directional solidification of the M g2Si in MATLAB. Microstructural parameters like the Secondary and Primary Dendritic Arm Spacing were studied to correlate the effects of processing parameters to the microstructure of M g2Si. / Master of Science / Thermoelectric generators are devices that transform heat energy into electricity, offering a way to capture and utilize waste heat for sustainable purposes. A cutting-edge manufacturing method called Selective Laser Melting (SLM) has shown great potential in creating high-performance materials like Bi2T e3 for thermoelectric applications. Researchers are now exploring the extension of this technique to other materials, such as Mg2Si. This study delves into the intricate process of melting and solidifying Mg2Si powders using SLM. Advanced computer models were created in MATLAB, to simulate these processes in detail. By employing Computational Fluid Dynamics (CFD) techniques, heat and fluid flow within the molten material was also closely examined. These simulations were vital for fine-tuning the printing settings used to fabricate Mg2Si powders via SLM. Moreover, a specialized model based on phase field theory was developed to mimic the solidification of Mg2Si. The effects of changing manufacturing parameters on the microstructure of the final product were examined. Understanding these microstructural aspects is crucial for optimizing the manufacturing process and ultimately enhancing the performance of Mg2Si for thermoelectric applications.