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At least 1,333 records · Page 74
All sourcesNASA NTRSDOE OSTI
NASA NTRSDate not supplied

Insights Into Reconstructing REE Compositions of Melt From Zircon-Melt Partition Coefficients Using Zircon-Hosted Melt Inclusions From the Yellowstone Volcanic Province

Establishing the major and trace element composition of the Earth’s melts (Hadean to recent) is essential for understanding crustal evolution. Due to its physical-chemical resilience, zircon spans the complete age spectra of Earth’s history, and thus provides the only physical record from the early Earth. However, the petrological context i.e., the melt from which zircon crystallised, is often lost, except for inclusions of melt preserved within zircon. Melt inclusions in zircon (MI) provide a valuable tool to constrain zircon-melt REE partition coefficients (D REE ), which are used with the zircon REE chemistry to reconstruct melt compositions. Such reconstruction requires accurate partition coefficients, which are particularly sensitive to temperature, but also to pressure and melt composition. We determined the major and trace element compositions of 60 co-existing zircon-MI pairs from two ~ 2 Ma age rhyolites (the caldera-forming Huckleberry Ridge Tuff; HRT-C and the post-caldera Blue Creek Flow; BC-1) of the Yellowstone Plateau volcanic field by EPMA and SIMS, and calculated a set of 60 zircon-MI partition coefficients. The MI from both units are glassy with average silica contents of 78.30 ± 0.74 and 77.19 ± 1.11 wt %, and Ti-in-zircon crystallisation temperatures are 839 ± 36 and 835 ± 35 oC. Measured D REE patterns for each population (n = 30) are tightly constrained and exhibit a smooth pattern spanning ~ six orders of magnitude from La to Lu, (with exceptions at Ce and Eu), and for the HRT exhibit greater curvature (i.e., flatter) between the MREE to HREE compared to the BC-1. D REE patterns for the HRT have small to moderate Ce anomalies (Ce/Ce* Di 50 ± 40), whereas those in the BC-1 are larger (98 ± 45), and both units exhibit negligible to positive Eu anomalies (Eu/Eu* Di 1.07 ± 0.89 and 1.80 ± 2.01, respectively). We compare the trace element compositions of the MI to bulk-glass compositions from Yellowstone to assess any differences, which are small, then compare the measured MI compositions to those reconstructed using published partition coefficients (natural, empirical and experimental). The choice of D REE for reconstruction of the melt REE pattern results in differing petrogenetic interpretations.

Laura J. Crisp↗
NASA NTRS2025

Enhancing Nasa Sounding Rocket Capabilities Through Composite Material Adoption

Sounding rockets are a suborbital research platform employed by NASA for heliophysics, astrophysics, and geospace science investigations, and for technology development. They follow semi-parabolic trajectories and are launched using surplus military, and commercial, solid-propellant rocket motors. NASA sounding rocket payloads are comprised of standard, modular subassemblies, designed to perform specific functions critical to achieving mission success criteria. Since the program’s inception, payload length and mass have trended upwards, limiting the capability of the platform to reach exospheric apogees and decreasing the time above critical altitudes to observe solar and celestial targets. To offset this trend, composite materials may be of use in payload and subsystem design to decrease payload mass. This investigation seeks to understand if there is a practical benefit to introducing composite materials on the NSRP by assessing mission specific impacts to those missions conducted in fiscal year 2024. To accurately estimate the mass of a composites-based payload, a standard subsystem (NIACS) underwent structural reconfiguration. Materials were selected that align with NSRP design, manufacturing, and testing standards. NIACS reconfiguration resulted in a mass reduction of 19.6% which was then applied to the payload system in entirety. Using vehicle performance carpet plots, delta apogee and time above the Kármán line were determined. Performance improvements were then evaluated against that mission’s success criteria to determine if that mission would have benefitted from using composite materials. On average, each mission would have gained 59.8 kilometers apogee and 62.9 seconds above the Kármán line. However, only nine of the seventeen missions would have benefitted from these performance improvements. Two of the missions could have used a lower-impulse launch vehicle to achieve mission success. Upleg stability met programmatic criteria; downleg instability and dynamic pressure improved, showing that ballast would not offset the mass reduction of using composite materials. Cost analysis showed that production costs will increase 39%. For the two missions that could have used a lower-impulse launch vehicle, the cost of the launch vehicle would have offset payload production costs. In summary, composite materials are not recommended for universal use on NASA sounding rocket payloads due to unclear programmatic benefits and added cost. However, they are justified for optical astrophysics and heliophysics missions, high-apogee (exosphere) requirements, or when they reduce payload costs versus higher impulse launch vehicles. Reflown, recoverable subsystems should use composites to enhance apogee and observation time.

Robert Henry Burth↗
NASA NTRS2026

Extrusion-based Additive Manufacturing of Regolith-Filled Shape Memory Vitrimer Composite for Lunar Construction

The National Aeronautics and Space Administration (NASA) is visiting the moon again. This time, the objective is to explore establishing a permanent lunar base. To achieve both longterm human habitation on the moon and future deep space travel, it is crucial to make the most of the in-situ resources and build autonomous systems on the moon to support the construction of a lunar habitat. NASA’s In-situ Resource Utilization (ISRU) program aims to minimize the need to ship heavy prefabricated structures, reducing cost and enhancing sustainability. Here, we developed an economical extrusion method for printing lunar regolith-based composites using shape memory vitrimer as a binder. A rheological study is conducted to determine the extrudability of the composite with different regolith weight percentages. Several characterizations were conducted on the composites. The as-printed composites exhibited compressive and flexural strengths of 73.32 MPa and 156.59 MPa, respectively, and good impact tolerance. The composite maintained 57.92% of its mechanical properties even after the second crack healing cycle. The composites also exhibit shape fixity ratio of 90.02% and shape recovery ratio of 83.46%. The simple synthesis method, sustainability, and good thermomechanical properties make the 3D printed composite an ideal material for lunar construction applications.

Kingsley Yeboah Gyabaah↗
DOE OSTI2016

3D Representative Volume Element Reconstruction of Fiber Composites via Orientation Tensor and Substructure Features

To provide a seamless integration of manufacturing processing simulation and fiber microstructure modeling, two new stochastic 3D microstructure reconstruction methods are proposed for two types of random fiber composites: random short fiber composites, and Sheet Molding Compounds (SMC) chopped fiber composites. A Random Sequential Adsorption (RSA) algorithm is first developed to embed statistical orientation information into 3D RVE reconstruction of random short fiber composites. For the SMC composites, an optimized Voronoi diagram based approach is developed for capturing the substructure features of SMC chopped fiber composites. The proposed methods are distinguished from other reconstruction works by providing a way of integrating statistical information (fiber orientation tensor) obtained from material processing simulation, as well as capturing the multiscale substructures of the SMC composites.

Li, Yi↗
DOE OSTI2018

Reversible adhesive compositions and related methods

The disclosure relates to reversible bonded structural joints using active adhesive compositions that can allow for dis-assembly, repair, and re-assembly. The disclosure is particularly directed to the adhesive composition material, irrespective of the type of the substrate(s) being joined. The adhesive composition can include any thermoplastic adhesive material that can be remotely activated for targeted heating of just the adhesive composition (e.g., and not the surrounding substrates being joined) via the inclusion of electromagnetically excitable particles in the adhesive composition. The substrates can be any metal material, any composite material, any hybrid material, or otherwise. The disclosed adhesive compositions allow for recyclability of parts at the end of their lifetime and repair/replacement of parts during their lifetime.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Carbon cladded composite flow field plate, bipolar plate and fuel cell

The present invention provides a carbon-cladded composite composition for use as a fuel cell flow field plate or bipolar plate. In one preferred embodiment, the composition comprises a core composite layer sandwiched between two clad layers, wherein (a) the clad layer comprises a conductive carbon or graphite material (e.g., carbon nano-tubes, nano-scaled graphene plates, graphitic nano-fibers, and fine graphite particles); (b) the core composite layer comprises a matrix resin and a conductive filler present in a sufficient quantity to render the composite layer electrically conductive with an electrical conductivity no less than 1 S/cm (preferably no less than 100 S/cm); and (c) the composition has a planar outer surface on each clad side having formed therein a fluid flow channel.

30 DIRECT ENERGY CONVERSION↗
DOE OSTI2020

Polymer composites for fused filament fabrication and methods of making the same

Disclosed are compositions of a fused filament fabrication (FFF) composite filament having embedded functional materials in a thermoplastic matrix. Methods of making the composite filaments are also disclosed. In one example, a FFF composite filament incorporates a MOF, in an amount greater than 10% by mass, dispersed in a matrix polymer. One example of a method of synthesizing FFF composite filaments involves mixing a suspension that has a MOF with a matrix polymer solution to yield a polymer-MOF mixture. The mixture is cast and dried into a solid composite material, which is formed a FFF composite filament having the MOF in an amount greater than 10% by mass.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Development of Composite Adsorbents for LLW Treatment and Their Adsorption Properties for Cs and Sr - 13127

In this study, the composite adsorbents (KCoFC-NM (NM: natural mordenite), KCoFC-SG (SG: porous silica gel), AMP-SG and so on) were prepared by impregnation-precipitation methods. As for the distribution properties, the largest K{sub d,Cs} value of 3.8 x 10{sup 4} cm{sup 3}/g was obtained for KCoFC-SG (Davi.) composite. KCoFC-SG (NH, MB5D) and T-KCFC also had relatively large K{sub d,Cs} values above 1.0 x 10{sup 4} cm{sup 3}/g. The uptake rate of Cs{sup +} ions was examined by batch method. KCoFC-SG (NH, MB5D) and AMP-SG (Davi.) had relatively large uptake rate of Cs{sup +}, and the uptake attained equilibrium within 1 h. The maximum uptake capacity of Cs{sup +} ions was estimated to be above 0.5 mmol/g for KCoFC-NM and KCoFC-CP composites. KCoFC-X composite had a relatively large uptake capacity of Cs{sup +} ions (0.23 mmol/g > 0.17 mmol/g (T-KCFC)) and this composite also had a selectivity towards Sr{sup 2+} ions; KCoFC-X is effective adsorbent for both Cs{sup +} and Sr{sup 2+} ions. The largest value of K{sub d,Sr} was estimated to be 218 cm{sup 3}/g for titanic acid-PAN. Titanic acid-PAN had the largest uptake rate of Sr{sup 2+} ions, and the uptake attained equilibrium within 8 h. Adsorbability of other nuclides was further examined by batch method. All adsorbents had adsorbability for Rb{sup +} and RuNO{sup 3+} ions. KCoFC-SG (NH), KCoFC-CP and T-KCFC had higher selectivity towards Cs{sup +} than other adsorbents; these adsorbents had adsorbability to Cs{sup +} ions even in the presence of Ba{sup 2+}, Ca{sup 2+} and Mg{sup 2+} ions. The separation factor of K{sub d,Sr}/K{sub d,Ba} for titanic acid-PAN was about 1, indicating that the K{sub d,Sr} for titanic acid-PAN tends to decrease with Ba{sup 2+} concentration. As for the breakthrough properties, the largest 5 % breakpoint and 5 % breakthrough capacity of Cs{sup +} ions were estimated to be 47.1 cm{sup 3} and 0.07 mmol/g for the column of KCoFC-SG (NH), respectively. The order of 5 % breakthrough capacity of Cs{sup +} is as follows; KCoFC-SG (NH) > KCoFC-NM > KCoFC-SG (Q-10) > T-KCFC > KCoFC-X > KCoFC-CP. From the results of batch and column experiments, the composite adsorbent of KCoFC-SG (NH) was effective for the uptake of Cs{sup +} ions, and KCoFC-X composite was useful for the uptake of both Cs{sup +} and Sr{sup 2+} ions. The estimation of irradiation stability and the uptake properties using the actual wastes are further essential for the practical operation. (authors)

36 MATERIALS SCIENCE↗
DOE OSTI2016

The synthesis and air oxidation behavior of U-Si-Al and U-Si-B compositions

Uranium silicide intermetallic compounds are currently under investigation by the DOE-NE Advanced Fuels Campaign as candidate accident tolerant nuclear fuel concepts for light water reactors. While many U-Si compounds offer benefits compared to reference UO{sub 2} in terms of heavy metal density and thermal conductivity, they have been shown to display poor resistance to oxidizing atmospheres above 400 Celsius degrees. The general oxidation behavior of all U-Si compounds is oxidation of uranium; formation of UO{sub 2} followed by U{sub 3}O{sub 8} leads to rapid pulverization of the material. It is hypothesized that introducing an additional compositional degree of freedom by exploring U-Si-X (X=Al or B) ternary systems may provide the means to design a candidate nuclear fuel which optimizes the benefits of each binary. Phase analysis and preliminary oxidation testing were performed on four compositions containing alloying additions to U{sub 3}Si{sub 2} and U{sub 3}Si{sub 5}. Aluminum additions to U{sub 3}Si{sub 2} were observed to increase the oxidation resistance by delaying the onset of oxidation during synthetic air ramp testing. U{sub 3}Al{sub 2}Si{sub 3} delayed the onset of oxidation to T>650 C. degrees. During a 10 hour isothermal hold at 400 C. degrees in air the compound gained very little mass, indicating that it could be stable at reactor operating temperatures. Further analysis of this material is necessary to determine its oxidation behavior in steam and determine the specific mechanism that is providing the delayed oxidation. Boron additions to U{sub 3}Si{sub 5} do not appear to provide any additional oxidation resistance to the compound as tested in this work. The 1.67 at.% addition of B produced primarily single-phase composition. Melting and sintering studies followed by further compositional and thermal analyses are required to advance this composition as a candidate composite fuel additive. Lastly, the nominally U{sub 3}BSi{sub 4} composition produced a multi-phase system which provided no additional oxidation resistance following either a synthetic air ramp oxidation test or a pre-passivation isothermal hold at 800 C. degrees.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2026

Neutrino Dipole Moments and Radiative Signatures from Partial Compositeness

We investigate composite neutrino models where heavy neutrinos emerge as bound states from a near-conformal strongly coupled sector. Standard Model neutrinos mix with these composite singlets via an inverse seesaw mechanism, where the anomalous scaling dimensions of the composite-sector operators naturally suppress light neutrino masses to sub-eV scales. Matching the conformal dynamics onto low-energy theory yields enhanced electromagnetic transition dipole operators with couplings $d_{μN} \sim 10^{-6}$-$10^{-8}\,\mathrm{GeV}^{-1}$, parametrically larger than the loop-level predictions of minimal Dirac or Majorana models. We carry out a dedicated event-level simulation of the production-and-decay chain $νX \to \mathcal{U} X \to νγX$ and compute the resulting event rates at MiniBooNE and MINERvA within the model, accounting for the composite production cross section and decay kinematics in detail. We further present predictions for the photon energy, angular, and multiplicity distributions. For the benchmark scenarios accessible at these experiments the radiative signal is predominantly single-photon; the composite structure additionally permits fragmentation of the up-scattered state into multiple heavy neutrinos, each decaying as $N\toνγ$, with multi-photon final states emerging for lighter compositeness scales or higher beam energies as a qualitatively new probe of the composite dynamics.

Assi, Benoît [Cincinnati U.; Fermilab] (ORCID:0000↗
DOE OSTI2019

Preparation of MgCo 2 O 4 /graphite composites as cathode materials for magnesium-ion batteries

Magnesium-ion batteries are fabricated with MgCo 2 O 4 /graphite composites as the cathode material. MgCo 2 O 4 nanoparticles are arranged using a co-precipitation method. A three-dimensional mixing process is utilized to mechanically decorate MgCo 2 O 4 nanoparticles on graphite particles. The MgCo 2 O 4 spinel crystals of size ranging from 20 to 70 nm on micrometer-sized graphite chunks are analyzed by using X-ray diffraction and scanning electron microscopy. The electrochemical properties of the as-prepared composites are well characterized by cyclic voltammetry, charge and discharge cycling, and electrochemical impedance spectroscopy (EIS). Interestingly, the MgCo 2 O 4 /graphite composite with a relatively low proportion of MgCo 2 O 4 , compared with the other as-prepared composites, achieves the highest specific capacity of 180 mAh g –1 at a C rate of 0.05 C. EIS results suggest that the electrical conductivity of the composite material is an increasing function of the graphite proportion. The superior performance of the MgCo 2 O 4 /graphite composite could be ascribed to the decoration of nanosized MgCo 2 O 4 particles as well as to the increased conductivity provided by graphite.

25 ENERGY STORAGE↗
DOE OSTI2019

Particle Strain Analysis of Epoxy-Based Composites Following Quasi-Static and Dynamic Compression

We investigate localized strains in polymer-based composites subjected to varying strain-rates and strains. Research on composites is often focused on their bulk mechanical behavior. However, many material phenomena are influenced by their microstructure, such as the mixing and reaction mechanisms of constituents in structural energetic materials. Therefore, the response of composites at the mesoscale is of clear interest; especially as insight into the micro-deformation and damage, and interaction effects between the constituents at the local level will better inform our understanding of the bulk composite constitutive behavior. To more fully understand the composite mechanical behavior at the mesoscale, uniaxial compression experiments were conducted on epoxy reinforced with aluminum (20 or 40 vol%) and nickel (0 or 10 vol%) particles. Additionally, the particle size of aluminum was either 5 or 50 μm in diameter. Experiments were carried out at quasi-static and dynamic strain rates. Resulting microstructures were analyzed to measure the degree of particle strain and compared to the global material strains for different degrees of strain-rate, strain, and particle size and volume fraction. The aluminum particle strain increased with global strain and had a strong dependency on strain rate. Introducing stiffer nickel particles resulted in larger aluminum particle strains. The nickel particle strain was minimal (< 3%) and showed no dependency with strain rate. This research gives insight into the interactions of particle reinforced composite constituents and their deformation at the mesoscale which is important for understanding phenomena such as preignition mechanisms in structural energetic materials.

36 MATERIALS SCIENCE↗
DOE OSTI2023

Core-shell structured tow-pregs enabled additive manufacturing of continuously reinforced thermoset composites

One of the major challenges in thermally curable polymer composite additive manufacturing is the slow curing time of thermally curable resins, coupled with a significant drop in thermoset viscosity upon heating, making the formation of complex shapes difficult. To tackle these issues, we have introduced a novel rapid composite preformation strategy called Tow-Preg Cladding (TPC). This technique involves the use of a thin and rapidly curable dual-cure resin, which combines a thermally curable resin (such as epoxy) with a fast photo-curable resin. The dual-cure resin is applied as a coating over a thermally curable resin tow-preg, enabling the formation of a rigid cladding that supports and shapes the tow-pregs into the desired geometries and patterns. The key advantage of this approach lies in the sequential formation of an interpenetrating polymer network (IPN) at the interlayer between laminates, resulting from the curing of the photocurable resin and the thermally curable resin sequentially. This IPN formation enhances interlaminar bonding in the composite, contributing to its overall strength and performance. The composites produced using this technique exhibited impressive mechanical properties, including longitudinal tensile strength of 1058.2 MPa, longitudinal tensile modulus of 74.2 GPa, flexural strength of 1080.4 MPa, and flexural modulus of 41.7 GPa. Overall, our Tow-Preg Cladding approach shows great promise in overcoming the challenges associated with thermally curable polymer composite additive manufacturing. It offers a viable solution to creating strong, shape-specific thermoset composites efficiently with enhanced mechanical properties.

42 ENGINEERING↗
DOE OSTI2016

Study of chloride ion transport of composite by using cement and starch as a binder

This study presents the chemical bonding and the structural properties of composites from accelerator chloride test migration (ACTM). The volume fractions between binder (cement and starch) and charcoal in composites are 20:80 and 60:40. The effect of the binder to the chemical composition, chemical bonding, and structural properties before and after chloride ion passing through the composites was determined by X-ray fluorescence (XRF), by Fourier transform infra-red (FTIR), and x-ray diffraction (XRD), respectively. From the XRD data, XRF data, and the FTIR data shows the amount of chemical composition, the type of binding, and the structure of composites are depending on the type of binder. The amount of chloride migration using starch as binder is higher than that of cement as a binder due to the density effects.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2025

Enhancing Thermal Transport in Polymeric Composites Via Engineered Noncovalent Filler–Polymer Interactions

Understanding thermal transport mechanisms in polymeric composites allows us to expand the boundaries of thermal conductivity in them, either increasing it for more efficient heat dissipation or decreasing it for better thermal insulation. But, these mechanisms are not fully understood. Systematic experimental investigations remain limited. Practical strategies to tune the interfacial thermal resistance (ITR) between fillers and polymers and the thermal conductivity of composites remain elusive. Here, we studied the thermal transport in representative polymer composites, using polyethylene (PE) or polyaniline (PANI) as matrices and graphite as fillers. PANI, with aromatic rings in its backbone, interacts with graphite through strong noncovalent π–π stacking interactions, whereas PE lacks such interactions. We can then quantify how π–π stacking interactions between graphite and polymers enhance thermal transport in composites. PE/graphite and PANI/graphite composites with the same 1.5% filler volume fractions show a ∼22.82% and ∼34.85% enhancement in thermal conductivity compared to pure polymers, respectively. Calculated ITRs in PE/graphite and PANI/graphite are ~6 x 10 -8 m 2 KW -1 and ~1 x 10 -8 m 2 KW -1 , respectively, highlighting how π–π stacking interactions reduce ITR. Molecular dynamics (MD) simulations suggest that π–π stacking interactions between PANI chains and graphite surfaces enhance alignment of PANI's aromatic rings with graphite surfaces. This allows more carbon atoms from PANI chains to interact with graphite surfaces at a shorter distance compared to PE chains. Finally, our work indicates that tuning the π–π stacking interactions between polymers and fillers is an effective approach to reduce the ITR and enhance the thermal conductivity of composites.

atoms↗
DOE OSTI2022

Understanding the Elastic, Plastic, and Damage Features in Fracturing of Self-reinforced Thermoplastic Composites via Non-destructive Digital Imaging Correlation

This work demonstrated the utilization of non-destructive Digital Imaging Correlation (DIC) method to characterize the elastic, plastic, and damage features during the Mode I intra-laminar fracturing process of self-reinforced thermoplastic composites by using a self-reinforced polypropylene (PP) composite as an example. The DIC results clearly showed the development of huge plastic zone (PZ) and non-negligible Fracture Process Zone (FPZ) in front of the notch tip during the fracturing process, and the geometries and sizes of the foregoing zones at the peak load were further quantified. Such an interesting fracturing behavior of self-reinforced thermoplastic composites is way different from brittle materials (e.g., glass, acrylic, etc.), ductile materials (e.g., aluminum, steel, etc.), and even quasi-brittle materials (e.g., concrete, nanoparticle-reinforced composites, tough ceramics, wood, cement, carbon/glass fiber-reinforced polymers, etc.). Thus, understanding the elastic, plastic, and damage features is the first step before better characterizing the material fracture properties of self-reinforced thermoplastic composites through new analytical methods and computational modeling. These efforts are of utmost importance for wide applications of self-reinforced thermoplastic composites in various engineering fields in the future.

Lightweight Composites, Self-reinforced Thermoplas↗
DOE OSTI2022

Improving the damage tolerance of Si 3 N 4 by forming laminate composites with refractory metals

The objective of this research was to demonstrate that the damage tolerance of Si 3 N 4 could be significantly improved by forming laminate composites with refractory metals, providing materials that undergo graceful failure, rather than the fast-fracture mechanism exhibited by monolithic Si 3 N 4 . A damage tolerant Si 3 N 4 could be used as a ring material in an all-ceramic bearing, decreasing the chance for catastrophic failure if the ring is stressed in tension during operation. The technical approach formed a laminate composite material using alternating Si 3 N 4 -metallic layers, with both outer layers being Si 3 N 4 to take advantage of its greater wear resistance, chemical stability, and thermal stability. The metallic layers are designed to arrest any cracks in the outer layers, thus producing a toughened Si 3 N 4 and avoiding the catastrophic failure behavior exhibited by monolithic ceramics. The laminate composites were fabricated using a combination of tape-casting Si 3 N 4 and metals from slurries, as well as metal foils, followed by hot pressing at 1500°C. The metallic materials employed were chromium, titanium, and tantalum. Analysis confirmed that the interfaces were well formed, and the laminates with chromium and titanium formed intermetallic compounds more readily than the composites with tantalum. The Si 3 N 4 -Ta laminates demonstrated crack deflection and bridging behavior during failure and flexural strength of 800–900 MPa. The hardness and elastic modulus of Si 3 N 4 -Ta laminates measured by nanoindentation were similar to those reported in literature. The hardness across the interface of the Si 3 N 4 -Ta composite varied according to the composition of the interface, which displayed a profile indicative of a diffusion bond.

36 MATERIALS SCIENCE↗
NASA NTRSDate not supplied

Composite Technologies for Science Missions

ASTROLAB, Lunar Geophysical Network, Mars Icebreaker and Mars PLACER Net missions propose use of various types of vehicles – such as rovers, landers and flying probes - to accomplish their scientific objectives. Although designs for such vehicles are myriad, many structural components can be made using composite manufacturing technologies. Composite materials are also myriad, by nature, but carbon fiber reinforced polymers (CFRP) in particular are sought after for their high specific strength and specific stiffness. CFRP components could be especially beneficial in vehicle designs for Moon or Mars missions due to their nearly negligible coefficient of thermal expansion (CTE). CTE is a critical design characteristics in environments where significant thermal swings are prevalent, such as those of atmosphere-less Moon and Mars.MSFC/EM42 houses several relevant composites technologies. Strong and rigid struts can be filament-wound. Shells and platforms can be laid-up using automated fiber placement (for repeatability) or by hand (for small features). Monolithic structures can even be designed to reduce part count and therefore reduce the risk of joint failures. Composites are also tailorable, allowing the incorporation of different material types or formats through the thickness of a part. This includes materials which shield from radiation or electrostatic discharge. Finally, the rigidity of composite parts minimizes overall vibration and compliance within a design.Additionally, missions such as Triton Ocean World Surveyor anticipate use of traditional, metallic fuel tanks. Composite overwrapped pressure vessels (COPVs) are suitable for use in this application as well. The Triton mission even cites a concern for heat retention, for which CFRP also offers improved characteristics over traditional metallic tanks.

Lightweight↗