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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.

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At least 595 records · Page 33
All sourcesNASA NTRSDOE OSTI
DOE OSTI2025

Structurally Driven Selective Adsorption of Hydrocarbons by Metal Substitution in Isostructural Rare-Earth Metal–Organic Frameworks

The design and realization of highly selective nanoporous materials are necessary to target critical separations across industries. By leveraging pore size, pore shape, and linker functionalization, the design of nanoporous solid adsorbents will enable the rapid production of energy efficient separation materials for high-value gas mixtures. This study uses a combination of modeling, synthesis, and gas adsorption testing to investigate a new class of small-pore isostructural rare-earth (RE) 2,5-dihydroxyterephthalic acid (DOBDC) metal–organic frameworks (MOFs) (RE: Pr-, Gd-, Er-, Yb; DOBDC = 2,5-dihydroxyterephthalic acid) and their adsorption selectivity for acetylene/ethylene mixtures. Density functional theory simulations identified that selective binding of acetylene over ethylene in the Gd-, Er-, and Yb-DOBDC MOFs was due to hydrogen-bonding between acetylene and the linker hydroxyl. Adsorption experiments validated the computational results by identifying mechanisms that control the acetylene/ethylene adsorption selectivity and high acetylene adsorption. Furthermore, dynamic column breakthrough experiments with the Gd-DOBDC MOF validated the simulations and indicated that ethylene can be separated from acetylene in a mixture containing 1 vol % acetylene and 39 vol % ethylene (balance argon). In conclusion, the results highlight the complexity of gas binding in functional porous materials and how combining modeling and experiment enables a fundamental understanding of gas–framework interactions that can be leveraged for the design of future separation materials.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2021

The quest for efficient oxygenated fuels: Examining interactions between lubricant components and oxygenates

This work empirically evaluated oxygenated blendstock-lubricant compatibility using a novel but simple method. The reactivity or compatibility was evaluated via gas chromatograph equipped with a flame ionization detector (GC-FID) before and after heating for 2h at 150 °C, which would roughly mimic conditions encountered in the combustion chamber of an Spark Ignition (SI) or Compression-Ignition (CI) engine. Five oxygenate blendstocks spanning several functional groups and chain lengths (prenol, isoprenol, butyl acetate, isohexanol, polyoxymethylene dimethyl ethers) were evaluated in a base fuel with nine variations of lubricant components of controlled concentrations, including fully formulated commercial lubricants. Baseline comparative examples were also generated, to decouple the effect of the oxygenate on the mixture, by heating only the base fuel with the lubricant component. Results demonstrate the relative compatibility between noted lubricants and oxygenates in base fuel upon heating. This was illustrated by minimal to no changes in the GC-FID traces. However, reactions of several of the chosen lubricants, especially Molybdenum di (2-ethylhexyl) phosphorodithioate (Molyvan L) and zinc dialkyldithiophosphate (ZDDP), with prenol and polyoxymethylene dimethyl ethers blendstocks showed substantial side reactions compared to corresponding baseline examples. Control experiments without oxygenates but comprising the same lubricant components showed no change in the mixture with heating. We concluded the incompatibility is due to the oxygenate and not the components of the base fuel. This preliminary work is valuable in establishing trends as well as provide useful information when a new component is introduced in the fuel.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
NASA NTRS1986

Origin of life and iron-rich clays

The premise that life began with self-replicating iron-rich clays is explored. In association with these clays and UV light, polar organic molecules, such as oxalic acid, were synthesized. The carbonaceous chondrites have both iron-rich clays and organic molecules. It is convenient to classify meteoritic organic matter into 3 categories: insoluble polymer, hydrocarbons and polar organics (soluble in water). Recent work on the delta D, delta N-15 and delta C-13 has made it clear that these three fractions have been made by three different mechanisms. A significant fraction of the insoluble polymer has a delta-D which suggests that it was made in an interstellar medium. The hydrocarbons seem to have been made on a parent body by a Fischer-Tropsch mechanism. The polar organics were probably synthesized in a mixture of carbonate (NH4)2CO3, Fe(++) ion and liquid water by radiolysis. In a set of experiments the radiolysis of (NH4)2CO3 in the presence and absence of Fe(++) ion has been examined. The synthesis of glycine in the presence of Fe(++) ion is 3-4 times that in the absence of ferrous ion. The effects of the addition of hydrocarbons to this mixture are explored. Iron-rich clays at low temperature and pressure are synthesized. So far the results are not sufficiently crystalline to look for replication. It should be noted that organic chelating agents such as oxalic acid do increase the crystallinity of the clays but not sufficiently. The hydrothermal synthesis of iron-rich clays is being examined.

Hartman, H. H.↗
NASA NTRS1984

A test to verify the biocompatibility of a method for plant culture in a microgravity environment

We report a pioneering attempt to use the NASA Shuttle Orbiter Middeck locker facility to acquire data on plant growth in near weightlessness. The information was needed to confirm the suitability of a plant culture system to be used in an experiment scheduled for the first Spacelab mission. The test was designed to measure germination and early seedling growth in a series of soil mixtures covering a range of water contents. Empirical determination of growth dependence on moisture content was required because both in theory and from Soviet flight experience it seemed possible that the dependence function in near weightlessness could be critically different from what we had measured on Earth. Such a difference could invalidate the future test in Spacelab 1 of gravity dependence of the differential growth process, circumnutation. After two failed attempts sufficient measurements were obtained from the third Shuttle Orbiter flight test to confirm the biocompatibility of the plant culture system--viz. soil moisture content variations had the same effect in near weightlessness as at 1 g. A number of supplemental observations about middeck locker conditions in Shuttle flight are presented. These may prove helpful to would-be experimenters who will plan to take advantage of future Shuttle flight opportunities for biological research.

Non-NASA Center↗
DOE OSTI2017

Influence of weakening minerals on ensemble strength and slip stability of faults: Influence of Weakening Minerals on Fault

We explore the impact of phyllosilicate (weak but velocity strengthening) in a majority tectosilicate (strong but velocity weakening) matrix on bulk shear strength and slip stability of faults. Numerical simple shear experiments using a distinct element model (DEM) are conducted on both uniform mixtures of quartz and talc analogs and on textured mixtures consisting of a talc layer embedded in a quartz matrix. The mechanical response of particles is represented by a linear elastic contact model with a slip-weakening constitutive relation representing the essence of rate-state friction. The weight percentage of the talc in the uniform mixtures and the relative thickness of the talc layer in the textured mixtures are varied to investigate the transitional behavior of shear strength and slip stability. Specifically, for uniform mixtures, ~50% reduction on bulk shear strength is observed with 25% talc present, and a dominant influence of talc occurs at 50%; for textured mixtures, a noticeable weakening effect is shown at a relative layer thickness of 1 particle, ~50% shear strength reduction is observed with 3-particles, and a dominant influence occurs at 5 particles. In terms of slip stability, a transition from velocity weakening to velocity strengthening is observed with 10% to 25% talc present in the uniform mixtures or with 3 particles to 5 particles in the textured mixtures. In addition, further analysis suggests that quartz has a high tendency toward dilation, potentially promoting permeability; while talc dilates with increased slip rate but compacts rapidly when slip rate is reduced, potentially destroying permeability. The simulation results match well with previous laboratory observations.

58 GEOSCIENCES↗
DOE OSTI2018

Isopiestic Determination of the Osmotic and Activity Coefficients of the { h H 2 SO 4 + (1– h )Al 2 (SO 4 ) 3 }(aq) System at T = 298.15 K. 1. Experimental Results at Stoichiometric Ionic Molality Factions h = (0.85777, 0.71534, 0.57337, 0.42985, 0.28593, and 0.14332)

Here, isopiestic vapor-pressure measurements have been made at 166 compositions of the { h H 2 SO 4 + (1– h )Al 2 (SO 4 ) 3 }(aq) system at the temperature 298.15 K using H 2 SO 4 (aq) as the isopiestic reference standard, where h is the stoichiometric ionic molality fraction of H 2 SO 4 in the mixtures that was calculated by assuming complete dissociation of both solutes. These experiments were performed up to the crystallization limits at values of h = (0.85777, 0.71534, 0.57337, 0.42985, 0.28593, and 0.14332) corresponding approximately to h = (6/7, 5/7, 4/7, 3/7, 2/7 and 1/7); the highest achieved molalities are very slightly above or close to the solubility limits because of the very limited tendency of Al 2 (SO 4 ) 3 to form supersaturated solutions when concentrated isothermally at 298.15 K.

36 MATERIALS SCIENCE↗
DOE OSTI2025

Scaled-up fabrication of durable and porous adsorbent-coated minichannels on aluminum for CO 2 separation

A method was developed to fabricate zeolite 13X adsorbent-coated minichannels on aluminum for CO₂ adsorption applications in this study. It emphasizes the innovative use of aluminum as a substrate, which offers airtight assembly, paving the way for highly efficient adsorption systems. An optimized coating process was developed using a slurry of Zeolite 13X, yeast, sugar, and xanthan gum, resulting in durable and highly porous layers that enhance CO₂ capture performance. A PETG peeler was designed to remove the top layer of the yeast-engineered adsorbent coatings, revealing a super porous and foamy structure. The teeth of the peeler were designed and fabricated for high repeatability and rapid prototyping. Breakthrough experiments were conducted on the scaled-up adsorbent bed using gas mixtures of 80% CO₂, 20% N₂, and 20% CO₂, 80% N₂ to represent different industrial scenarios. The performance of the bed was evaluated at flow rates of 160 and 190 cm³ min -1 using a Raman Laser Gas Analyzer (RLGA), demonstrating stable adsorption without degradation across multiple cycles. Computational modeling of integral transport phenomena under the chosen experimental conditions was pursued using gPROMS ProcessBuilder™, and the modeling results were compared with those from the tests for adsorption time, which resulted in an error margin of 2% to 9% for the breakthrough time, confirming the easy reproducibility of the design through modeling. This research advances CO₂ capture technologies by providing an effective and scalable solution for producing aluminum-based adsorbent coated beds, supporting industrial carbon capture efforts.

CO2 capture↗
DOE OSTI2019

A new Transition Radiation detector based on GEM technology

Transition Radiation Detectors (TRD) have the potential feature of separating particles by their gamma factor. Classical TRDs are based on Multi-Wire Proportional Chambers (MWPC) or straw tubes, using a Xenon based gas mixture to efficiently absorb transition radiation photons. These detectors operate well in experiments with relatively low particle multiplicity. The performance of MWPC-TRD in experiments with luminosity of order 10 34 cm 2 s –1 and above, is significantly deteriorated due to the high particle multiplicity and channel occupancy. Replacing MWPC or straw tubes with a high granularity Micro Pattern Gas Detectors (MPGD) like Gas Electron Multipliers (GEMs), could improve the performance of the TRD. In addition, GEM technology allows one to combine a tracker with TRD identification (GEM-TRD/T). This report presents a new TRD development based on GEM technology for the future Electron Ion Collider (EIC). The first beam test was performed at Jefferson Lab (Hall-D) using 3–6 GeV electrons. A GEM-TRD/T module has been exposed to electrons with and without a fiber radiator. First results of test beam measurements and comparison with Geant4 Monte Carlo are introduced here.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2021

Modeling molybdeneum-99 production in molten salt reactors

Molten salt reactors (MSRs) are being investigated as a possible source of 99 Mo for medical uses. This paper describes computational modeling being performed to determine the feasibility for use of several MSR concepts in 99 Mo production: the Molten Salt Breeder Reactor (MSBR), the Molten Salt Demonstration Reactor (MSDR), and the Molten Salt Reactor Experiment (MSRE). This modeling is accomplished with SCALE/TRITON using a three-mixture system and estimated removal terms. Results showed that the MSBR, MSDR and MSRE were capable of supplying an estimated 35,800,000, 13,700,000, and 132,000 six-day Ci/week of 99 Mo, respectively, which is far more than the global demand. In conclusion, a range of operating parameters has been determined in which each reactor type is expected to have sufficient production capability to meet global demand.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗
DOE OSTI2020

Combustion of Silane-Hydrogen-Nitrous oxide Mixtures: Analysis of Laminar Flame Propagation and Condensed Products

The laminar burning rate, the explosion pressure, and the pressure rise coefficient have been measured for silane-nitrous oxide-argon mixtures using the spherically expanding flame technique in a constant volume combustion chamber. For these three parameters, the values obtained were higher than for hydrogen-nitrous oxide-argon and typical hydrocarbon-based mixtures. As an example, a maximum burning rate of 1800 g/m 2 s was measured at 101 kPa, whereas under similar conditions, a maximum burning rate around 950 g/m 2 s has been reported for hydrogen-nitrous oxide-argon mixtures. Here, the condensed combustion products formed in the silane-nitrous oxide-argon flames were sampled and characterized using electron micrograph, electronic diffraction, energy-dispersive spectroscopy, and X-ray powder diffraction. For all equivalence ratios, silica spherical particles with a mean diameter in the range 200-300 nm were observed. In addition, for mixtures with Φ ≥2.2, silicon nanowires were formed. X-ray diffraction experiments showed that the silicon nanowires are composed of a material referred to as “metal silicon” characterized by a cubic structure (lattice parameter: a = 5.425 Å) with the Fm-3m space group.

42 ENGINEERING↗
DOE OSTI2021

Single Quadrupole Multiple Fragment Ion Monitoring Quantitative Mass Spectrometry

Single quadrupole mass spectrometry (MS) with enhanced in-source multiple fragment ion monitoring was designed to perform high sensitivity quantitative mass analyses. Enhanced in-source fragmentation amplifies fragmentation from traditional soft electrospray ionization producing fragment ions that have been found to be identical to those generated in tandem MS. We have combined enhanced in-source fragmentation data with criteria established by the European Union Commission Directive 2002/657/EC for electron ionization single quadrupole quantitative analysis to perform quantitative analyses. These experiments were performed on multiple types of complex samples that included a mixture of 50 standards, as well as cell and plasma extracts. The dynamic range for these quantitative analyses was comparable to triple quadrupole multiple reaction monitoring (MRM) analyses at up to 5 orders of magnitude with the cell and plasma extracts showing similar matrix effects across both platforms. Amino acid and fatty acid measurements performed from certified NIST 1950 plasma with isotopically labeled standards demonstrated accuracy in the range of 91–110% for the amino acids, 76–129% for the fatty acids, and good precision (coefficient of variation <10%). To enhance specificity, a newly developed correlated ion monitoring algorithm was designed to facilitate these analyses. This algorithm autonomously processes, aligns, filters, and compiles multiple ions within one chromatogram enabling both precursor and in-source fragment ions to be correlated within a single chromatogram, also enabling the detection of coeluting species based on precursor and fragment ion ratios. Single quadrupole instrumentation can provide MRM level quantitative performance by monitoring/correlating precursor and fragment ions facilitating high sensitivity analysis on existing single quadrupole instrumentation that are generally inexpensive, easy to operate, and technically less complex.

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

Liquid Sorption-Enhanced Haber–Bosch Process

The use of a liquid sorbent in a traditional Haber-Bosch process enables significant improvements in energy efficiency and potential cost savings for arguably the most important chemical process on the planet. The approach presented in this report employs an incompressible liquid sorbent that absorbs and releases ammonia (NH 3 ) under specific conditions. To achieve this, we investigate reactions of ammonia and pure phosphoric acid (H 3 PO 4 , PA), which rapidly neutralize to form an equilibrated solution of monoammonium phosphate (MAP) and diammonium phosphate (DAP) that functions as a reversible and regenerable sorbent. Through intimate contact of the gas-phase Haber-Bosch reaction mixture with this liquid absorbent, complete equilibrium uptake may be achieved in an appropriately sized separator, and facile separation occurs through the use of independent liquid and gas phases. Following depressurization and release of the ammonia product, only the incompressible fluid needs to be repressurized and returned to the reactor. This study documents proof-of-concept absorption and desorption experiments carried out in 75 mL batch reactors, predominantly charged with precise MAP and DAP mixtures that equilibrate at process-relevant temperatures and pressures. We then assemble the first thermodynamic relationships that underlie this advantaged separation strategy, validated by reactive force field (ReaxFF) interatomic potential simulations, and benchmarked with traditional separation routes via process modeling and technoeconomic analysis. The scale of energy consumption in the century-old Haber-Bosch process is massive, and the elegant liquid sorption approach reported here offers opportunities to enhance its energy efficiency for the next frontier of ammonia synthesis.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2016

Construction and experimental validation of a simple, compact, resealable, and reliable Vycor{sup ®} superleak assembly for use at low temperatures

A new method of constructing a superleak assembly for use in experiments involving {sup 4}He or {sup 3}He-{sup 4}He mixtures at very low temperatures is described. Superleaks are made of a porous medium with very small pores and channels. Superleaks are often incorporated in thermomechanical pumps, superfluid magnetic pumps, dilution refrigerators, and superfluid helium transfer systems. We used several cylindrical pieces of Vycor, a permeable glass with average pore diameter of 40 Å and porosity of 28%, as a candidate to be used in our superleak assembly. Our design is simple and compact. Our superleak assembly can be disassembled and easily reassembled for reuse. We successfully tested and validated this device at temperatures between 1.4 K and 2.7 K. We experienced no superfluid leaks into the surrounding vacuum. We also report that thermal cycling caused no performance degradation. It is our goal to share the design and construction techniques of this new superleak assembly.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2026

The MuFusE large-volume diamond anvil cell for exploring muon-catalyzed fusion at higher pressures and temperatures

A new large-volume diamond anvil cell (DAC) has been developed for the Muon-catalyzed Fusion (μCF) Experiment (MuFusE), enabling the compression and heating of deuterium–tritium (d–t) mixtures to pressures and temperatures needed to advance μCF research. The MuFusE DAC achieves the large sample volumes necessary for high-precision fusion measurements while integrating cryogenic loading, all-metal sealing, and flexible bellows to maintain a secure environment during cell compression. Combined with remote pneumatic actuation and secondary containment, the DAC safely managed a 25 Ci tritium inventory while providing a clear optical path for in situ measurements of sample pressure and composition via laser spectroscopy. Utilizing 5 mm diameter diamond anvils oriented in the path of a high-intensity muon beam, the apparatus achieved a stable sample volume of 19.2 mm 3 at liquid density, pressures up to 933 MPa and temperatures up to 400 K—benchmarks that significantly exceed previously reported limits for static d–t targets.

Kalow, J. D. [Acceleron Fusion, Inc., Cambridge, M↗
DOE OSTI2019

Chemical Kinetic Effects on Detonation Wave Generation in a Semi-Bounded Channel

The coupled effects of mixing and ignition are investigated in a semi-bounded channel that emulates a rotating detonation engine geometry. In previous studies, a robust mechanism of self-excited detonation wave generation was discovered with O 2 /CH 4 reactants in this experiment. The behavior requires symbiosis between the chemical kinetics of the reactant mixture and the dynamics of the reactant injection process. The reactant jet dynamics are controlled principally by the geometry of the system and the pressure differences across the injector. The chemical kinetics are modified by changing the reactant composition to investigate how the combustion behavior changes when the kinetics become the rate-controlling process. Ignition delay timescales are increased by introducing an inert gas, N 2 , to the oxidizer flow; conversely, ignition delay time-scales are decreased by replacing natural gas fuel with hydrogen, H 2 . The effects of the oxidizer modifications to the chemical kinetics for each fuel are studied independently to characterize the amplification process associated with the self-excited instability, and apply this understanding to the sustainability of detonations in a comparable RDE environment.

20 FOSSIL-FUELED POWER PLANTS↗
NASA NTRS1974

Test results on the Viking gas chromatograph-mass spectrometer experiment

The gas chromatograph-mass spectrometer instrument to be utilized in the Viking 1975 Molecular Analysis experiment has undergone preliminary testing in its flight configured version. A synthetic mixture of 24 components as well as a sample of the Murchison meteorite has been used for this purpose. The resulting data not only allowed the identification of most of the organic compounds known to be present, but also revealed the identity of a few unexpected ones. Thus, the sensitivity and reliability of the instrument and data system are satisfactorily demonstrated.

Biemann, K.↗
NASA NTRS1978

Direct nuclear pumping by a volume source of fission fragments

A detailed kinetic model is presented for the analysis of nuclear pumped lasers when the pumping is a result of a volume source of fission fragments. The results of the model are employed to study a He-3 - Xe laser. For the range of pressures, neutron fluxes and mixtures considered, the gain and power calculations are in good agreement with experiment. Moreover, based on these calculations, it appears that the collisional recombination is the dominant pumping mechanism for 7p-7s transitions while direct excitation is the dominant pumping mechanism for the 5d-6p transitions.

Deese, J. E.↗