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A new metric was developed to quantify the impact of surface-connected defects and internal pores of different morphologies, namely irregular lack of fusion (LoF) pores and spherical keyhole pores, on the mechanical properties and fracture location of AlSi10Mg tensile samples fabricated using laser powder bed fusion additive manufacturing. As defect volume alone has been shown to be insufficient to predict fracture location, the proposed defect impact metric (DIM) incorporates contributions from additional defect features, including proximity to the surface, interaction with neighboring defects, morphology, and reduction in load-bearing cross-sectional area to better assess a defect’s propensity for corresponding to fracture location. The fracture location of keyhole samples was captured by large surface-connected defects with numerous neighboring defects and resulted in increased losses in load-bearing area. In contrast, LoF samples fractured at regions with either large surface-connected defects or large internal pores with many defects in close proximity, high curvatures, and large projected areas. The proposed DIM outperformed existing defect-based frameworks in identifying fracture locations in both LoF and keyhole samples by incorporating surface roughness, defect projected area, and interactions between defects based on distance, volume, and configuration. Additionally, the maximum DIM value within the fracture range was more strongly correlated to strength and ductility than porosity or defect size for LoF samples, demonstrating the potential of the DIM to non-destructively assess the effects of defects on mechanical behavior. The broader applicability of the DIM framework was demonstrated in its ability to capture fracture in both PBF-LB AlSi10Mg and Alloy 718. 

Additively manufactured metals often contain pores, which limit the strength and ductility of resulting components. In this study, a ductile fracture model was developed to describe the effect of pore size, in terms of absolute and relative metrics, on fracture strain under uniaxial tension. The model approximates lack of fusion (LoF) pores as penny-shaped cracks, and damage accumulation was based on the J-integral and secondary Q parameter. The model was calibrated with Ti-6Al-4V samples with intentionally introduced pores fabricated by laser powder bed fusion (PBF-LB) additive manufacturing (AM) in as-built and heat-treated conditions. The model captures the experimentally observed size effect, where for a given pore area fraction, larger samples fracture at smaller strains. By identifying the critical pore size for a single, isolated pore for either load or displacement-controlled applications, the model developed in this study is a crucial step to developing a comprehensive fracture model for establishing confidence in the structural capability of pore-containing additively manufactured components. 

Multicomponent refractory alloys have the potential to operate in high-temperature environments. Alloys with heterogeneous/composite microstructure exhibit an optimal combination of high strength and ductility. The present work generates designed compositions using high-throughput computational and machine-learning (ML) models based on elements Mo-Nb-Ti-V-W-Zr manufactured utilizing vacuum arc melting. The experimentally observed phases were consistent with CALPHAD and Scheil simulations. ML models were used to predict the room temperature mechanical properties of the alloy and were validated with experimental mechanical data obtained from the three-point bending and compression tests. This work collectively showcases a data-driven, inverse design methodology that can effectively identify new promising multicomponent refractory alloys. 

This study investigates the effects of pores on the mechanical properties of metals produced by additive manufacturing, which can limit strength and ductility. This research aims to both measure and model the rate of crack growth emanating from these pores in additively manufactured Ti-6Al-4 V fabricated with laser powder bed fusion. Uniaxial tensile samples containing intentionally embedded penny-shaped pores were mechanically tested to failure, and loading was interrupted by a series of unload steps to measure the stiffness degradation with load. The factors contributing to reduction in stiffness, namely (1) elastic and plastic changes to geometry, (2) the effect of plastic deformation on modulus, and (3) crack growth, were deconvoluted through finite element modeling, and the crack size was estimated at each unloading step. The stiffness-based method was able to detect stable crack growth in samples with large pores (1.6% to 11% of the cross-sectional area). Crack growth as a function of strain was fit to a model where the crack driving force was based on equivalent strain and a model where the crack driving force was based on energy release rate. Significant crack growth occurred only after the onset of necking in samples containing small pores, while samples containing large pores experienced continuous crack growth with strain. 

Ultra-high temperature ceramics (UHTCs) are refractory transition-metal carbides, nitrides, and borides with the highest melting temperatures known materials, making them prime candidates for applications in aerospace and hypersonic vehicles. Of the UHTCs, tantalum carbide (TaC) and hafnium carbide (HfC) feature the highest melting temperatures. We investigated the binderless consolidation of HfC/TaC powder blends using Field Assisted Sintering Technology (FAST). Powders consisting of 90/10, 50/50, and 10/90 vol% HfC:TaC were sintered to high densities (>94 %). Bulk and nanomechanical, chemical, and microstructural characterization revealed substantially greater strength, hardness, and stiffness for ternary alloys. Mechanical properties correlated with physiochemical analysis indicated trace oxygen phases, solid-solution strengthening, and nonstoichiometric carbon were the key mechanisms driving the peak property enhancement of the 50 vol% solid-solution sample, despite lower densities. This study provides insight into optimizing the compositional design of HfC-TaC alloys by balancing influences from solid solution strengthening and the thermodynamic effects of oxygen/carbon stoichiometry. 

The microstructure, phase behavior, mechanical properties, and corrosion properties of a series of Al10Cr15(Fe3Mn)75−x(Ni)x medium-entropy alloys (MEAs) spanning 0–20 at% Ni were studied to elucidate the chemistry-structure-property relationship of this system as a function of Ni content. This work demonstrates that from an initial BCC phase Al10Cr15(Fe3Mn)75 MEA, Ni additions of 5 and 10 at% result in the formation of ordered B2-phase precipitates due to interaction of Ni with Al, resulting in high hardness (∼475 HV). Further Ni addition to 15 at% leads to a dual-phase FCC+BCC structure, with B2 phase precipitates distributed in the BCC matrix relatively rich in Al and Ni but depleted in Cr. This dual-phase structure has a high yield strength (YS) of 600 MPa with a total elongation of 15%. Additionally, the B2 precipitates in BCC phase serve as preferential sites for corrosion in 0.6 M NaCl. Increasing Ni content to 20 at% results in lower YS of 300 MPa, but a significant improvement in ductility and corrosion resistance due to the increased FCC phase fraction. 

Molybdenum and its alloys are of interest for applications with extreme thermomechanical requirements such as nuclear energy systems, electronics, aerospace vehicles, and hypersonic vehicles. In the present study, pure molybdenum and samples with added hafnium carbide (HfC) grain refiners were produced using field assisted sintering technology (FAST). The molybdenum and HfC reacted with oxygen to produce MoO2 and HfO2, and increased HfC content from 1 wt% to 5 wt% decreased grain size while the microhardness correspondingly increased. Room temperature three-point bending tests were conducted, and finite element modeling was used to define HfC-dependent bilinear material models. The presence of oxygen most severely affected pure molybdenum, which exhibited little strength and limited ductility, whereas for samples with added HfC, HfO2 was present, resulting in increased toughness hypothesized to be due to microcrack toughening. The samples with 1 wt% added HfC had the greatest energy absorption capability. 

The tunable properties of thermoplastic elastomers (TPEs), through polymer chemistry manipulations, enable these technologically critical materials to be employed in a broad range of applications. The need to “dial-in” the mechanical properties and responses of TPEs generally requires the design and synthesis of new macromolecules. In these designs, TPEs with nonlinear macromolecular architectures outperform the mechanical properties of their linear copolymer counterparts, but the differences in deformation mechanism providing enhanced performance are unknown. Here, in situ small-angle X-ray scattering (SAXS) measurements during uniaxial extension reveal distinct deformation mechanisms between a commercially available linear poly(styrene)-poly(butadiene)-poly(styrene) (SBS) triblock copolymer and the grafted SBS version containing grafted poly(styrene) (PS) chains from the poly(butadiene) (PBD) mid-block. The neat SBS (φSBS = 100%) sample deforms congruently with the macroscopic dimensions with the domain spacing between spheres increasing and decreasing along and traverse to the stretch direction, respectively. At high extensions, end segment pullout from the PS-rich domains is detected, which is indicated by a disordering of SBS. Conversely, the PS-grafted SBS that is 30 vol% SBS and 70% styrene (φSBS = 30%) exhibits a lamellar morphology and in situ SAXS measurements reveal an unexpected deformation mechanism. During deformation there are two simultaneous processes: significant lamellar domain rearrangement to preferentially orient the lamellae planes parallel to the stretch direction and crazing. The samples whiten at high strains as expected for crazing, which corresponds with the emergence of features in the two-dimensional SAXS pattern during stretching consistent with fibril-like structures that bridge the voids in crazes. The significant domain rearrangement in the grafted copolymers is attributed to the new junctions formed across multiple PS domains by the grafts of a single chain. The in situ SAXS measurements provide insights into the enhanced mechanical properties of grafted copolymers that arise through improved physical crosslinking that leads to nanostructured domain reorientation for self-reinforcement and craze formation where fibrils help to strengthen the polymer.