Search NASA⌕ Search

SEARCH · Search NASA

Results for “Assembly”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 217 records · Page 12
All sourcesNASA NTRSDOE OSTI
DOE OSTI2023

Cooling assembly for a turbine assembly

A cooling assembly includes a coolant chamber disposed inside an airfoil of a turbine assembly that directs coolant inside the airfoil. The airfoil extends between a leading edge and a trailing edge along an axial length of the airfoil. Inlet cooling channels are fluidly coupled with the coolant chamber and direct the coolant in a direction toward a trailing edge chamber of the airfoil. The trailing edge chamber is fluidly coupled with at least one inlet cooling channel. The trailing edge chamber is disposed at the trailing edge of the airfoil and includes an inner surface. The inlet cooling channels direct at least a portion of the coolant in a direction toward the inner surface of the trailing edge chamber. One or more outlet cooling channels direct at least a portion of the coolant in one or more directions away from the trailing edge chamber.

Rathay, Nicholas William↗
DOE OSTI2018

Polyethylene-Glycol-Mediated Self-Assembly of Magnetite Nanoparticles at the Liquid/Vapor Interface

It is shown that magnetite nanoparticles (MagNPs) grafted with polyethylene glycol (PEG) self-assemble and short-range-order as 2D films at surfaces of aqueous suspensions by manipulating salt concentrations. Synchrotron X-ray reflectivity and grazing-incidence small angle X-ray scattering studies reveal that K 2 CO 3 induces the migration of the PEG-MagNPs to the liquid/vapor interface to form a Gibbs layer of monoparticle in thickness. As the salt concentration and/or nanoparticle concentration increase, the surface-adsorbed nanoparticles become more organized. And further increase in salt concentration leads to the growth of an additional incomplete nanoparticle layer contiguous to the first one at the vapor/liquid interface that remains intact.

36 MATERIALS SCIENCE↗
DOE OSTI2016

The Key Role of U 28 in the Aqueous Self‐Assembly of Uranyl Peroxide Nanocages

Abstract For 11 years now, the structural diversity and aesthetic beauty of uranyl–peroxide capsules have fascinated researchers from the diverse fields of mineralogy, polyoxometalate chemistry, and nuclear fuel technologies. There is still much to be learned about the mechanisms of the self‐assembly process, and the role of solution parameters including pH, alkali template, temperature, time, and others. Here we have exploited the high solubility of the UO 2 2+ /H 2 O 2 /LiOH aqueous system to address the effect of the hydroxide concentration. Important techniques of this study are single‐crystal X‐ray diffraction, small‐angle X‐ray scattering, and Raman spectroscopy. Three key phases dominate the solution speciation as a function of time and the LiOH/UO 2 2+ ratio: the uranyl–triperoxide monomer [UO 2 (O 2 ) 3 ] 4− and the two capsules [(UO 2 )(O 2 )(OH)] 24 24− (U 24 ) and [(UO 2 )(O 2 ) 1.5 ] 28 28− (U 28 ). When the LiOH/U ratio is around three, U 28 forms rapidly and this cluster can be isolated in high yield and purity. This result was most surprising and challenges the hypothesis that alkali templating is the most important determinant in the cluster geometry. Moreover, analogous experiments with KOH, NH 4 OH, and TEAOH (TEA=tetraethylammonium) also rapidly yield U 28 , which suggests that U 28 is the kinetically favored species. Complete mapping of the pH–time phase space reveals only a narrow window of the U 28 dominance, which is why it was previously overlooked as an important kinetic species in this chemical system, as well as others with different counterions.

Falaise, Clément↗
DOE OSTI2018

Equilibration of Imine-Linked Polymers to Hexagonal Macrocycles Driven by Self-Assembly

Macrocyclesbased on directional bonding and dynamic covalentbond exchange can be design ed with specificpore shapes, sizes, andfunctionality.These sys- tems retain many of the design criteria and desirableas- pects of two-dimensional (2D) covalent organic frame- works (COFs)but are more easily processed. Here we access discrete hexagonal imine-linked macrocycles by condensing atruncated analogueof1,3,5-tris(4-aminophe- nyl)benzene(TAPB) with terephthaldehyde (PDA). The monomers first condense into polymers buteventually convertinto hexagonal macrocycles in high yield. The high selectivity for hexagonal macrocycles is enforcedby their aggregation and crystallization into layered struc- tures with more sluggish imine exchange. Their formation and exchange processes provide new insight into how imine-linked 2D COF simultaneously polymerize and crys- tallize. Solutions of theseassembled macrocycles were cast into oriented, crystalline films, expanding the poten- tial routes to 2D materials.

covalent organic frameworks↗
DOE OSTI2021

Supramolecular Interactions and Morphology of Self-Assembling Peptide Amphiphile Nanostructures

The morphology of supramolecular peptide nanostructures is difficult to predict given their complex energy landscapes. We investigated peptide amphiphiles containing β-sheet forming domains that form twisted nanoribbons in water. We explained the morphology based on a balance between the energetically favorable packing of molecules in the center of the nanostructures, the unfavorable packing at the edges, and the deformations due to packing of twisted β-sheets. We find that morphological polydispersity of PA nanostructures is determined by peptide sequences, and the twisting of their internal β-sheets. Here, we also observed a change in the supramolecular chirality of the nanostructures as the peptide sequence was modified, although only amino acids with l-configuration were used. Upon increasing charge repulsion between molecules, we observed a change in morphology to long cylinders and then rodlike fragments and spherical micelles. Understanding the self-assembly mechanisms of peptide amphiphiles into nanostructures should be useful to optimize their well-known functions.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Block Copolymers: Synthesis, Self-Assembly, and Applications

Research on block copolymers (BCPs) has played a critical role in the development of polymer chemistry, with numerous pivotal contributions that have advanced our ability to prepare, characterize, theoretically model, and technologically exploit this class of materials in a myriad of ways in the fields of chemistry, physics, material sciences, and biological and medical sciences. The breathtaking progress has been driven by the advancement in experimental techniques enabling the synthesis and characterization of a wide range of block copolymers with tailored composition, architectures, and properties. In this review, we briefly discussed the recent progress in BCP synthesis, followed by a discussion of the fundamentals of self-assembly of BCPs along with their applications.

applications↗
DOE OSTI2020

Evaporative Assembly: Dual-Scale Nanostructures via Evaporative Assembly (Adv. Mater. Interfaces 7/2020)

In article number 1901954, Sunita Srivastava, Surita R. Bhatia, and co-workers demonstrate that evaporative assembly of functionalized nanoparticles can yield striking dual-scale hierarchical structures. Regular microscale stripes of nanoparticle monolayers with hexagonal nanoscale order are obtained on physically and chemically homogeneous substrates through evaporation of a suspension of DNAfunctionalized nanoparticles with a charged shell. The stripe width, spacing and nanoparticle ordering can be controlled by varying nanoparticle concentration and can be described by a simple analytical model. The results indicate that the interplay between “stick-slip” motion of the droplet contact line and Coulombic and steric nanoparticle interactions control the formation of the observed structures. Finally, this work demonstrates a simple cost-effective mask-free method for fabricating nanostructured 2D materials and metasurfaces for applications ranging from energy conversion/storage to optoelectronics and nanophotonics.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2021

Optimizing the self-assembly of conjugated polymers and small molecules through structurally programmed non-covalent control

Organic conjugated polymers and oligomers are key electronic materials for applications such as transistors, photovoltaics, and light emitting devices due to their potential for solution processability, mechanical flexibility, and precise structure-based tuning compared to inorganic materials. In dilute environments, the optoelectronic properties of conjugated polymers are largely governed by their constitutional structure and, to a lesser degree, their solution-state intramolecular configuration. In the solid state, intramolecular conformation and intermolecular electronic coupling impact these properties substantially, especially in relation to device performance. Therefore, an increasingly important area of research concerning conjugated materials is developing design strategies aimed at optimizing the solid-state packing for electronic applications. Programming solid-state packing arrangements through discrete non-covalent interactions is an emerging strategy within the context of conjugated polymers. This review focuses on the use of the two most prevalent discrete and directional interactions used to dictate the self-assembly of conjugated polymers and oligomers—hydrogen bonds and chalcogen bonds. Further, we also discuss how these design motifs can imbue conjugated materials with appealing physical properties while simultaneously retaining or improving electronic capabilities.

36 MATERIALS SCIENCE↗