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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 1,423 records · Page 79
All sourcesNASA NTRSDOE OSTI
DOE OSTI2025

Current understanding of Oxidative Coupling of Methane (OCM) reaction over supported Mn-Na 2 WO 4 catalysts

This perspective reviews the current understanding of the Oxidative Coupling of Methane (OCM) reaction over the supported Mn-Na 2 WO 4 /SiO 2 catalyst, with a focus on recent insights gained from state-of-the-art in-situ and operando spectroscopic characterization and chemical probe experiments under controlled environments. The supported Mn-Na 2 WO 4 /SiO 2 catalyst exhibits dynamic structural changes during the OCM reaction, involving multiple reactive lattice and adsorbed oxygen species, each associated with different oxide phases. These oxygen species play distinct roles in various steps of the OCM mechanism. The catalytic active sites for activation of CH 4 are associated with isolated surface Na-WO x sites on the SiO 2 support and the role of surface MnO x sites on SiO 2 is to oxidatively dehydrogenate C 2 H 6 to C 2 H 4 . Furthermore, this paper provides a detailed discussion of these roles and also introduces new experimental data from Temporal Analysis of Products (TAP) studies to clarify the ongoing debate in the literature regarding the contributions of lattice versus adsorbed oxygen species in OCM reaction product formation. Additionally, recommendations are offered for optimizing the performance of supported Mn-Na 2 WO 4 /SiO 2 catalysts to enhance CH 4 activation and C 2 product selectivity.

03 - NATURAL GAS↗
DOE OSTI2021

Coupled uptake and conversion of C 12 H 26 and NO on Pd/SSZ-13: Experiments and modeling

The uptake of NO in the presence of C 12 H 26 (dodecane) and H 2 O over a Pd/SSZ-13 washcoated Passive NOx Adsorber (PNA) monolith is reported. When a co-feed containing C 12 H 26 and NO is supplied to an unsaturated (with C 12 H 26 ) sample, the NO uptake is unaffected but during the subsequent temperature ramp the release of trapped NO is delayed from 175°C to over 220°C. The release delay is beneficial for PNA performance as the primary NO x aftertreatment technology, Selective Catalytic Reduction (SCR), is not operated below 200°C. However, pre-saturation of C 12 H 26 followed by the same NO and C 12 H 26 co-feed results in a decrease in the NO uptake compared to the NO-only feed. We conjecture that C 12 H 26 pre-adsorbed on the exterior surface of the sample blocks NO access to the pores, decreasing the number of available sites for NO uptake. Oxidation of C 12 H 26 leads to the generation of partial oxidation product CO at lower temperatures (<250°C) and deep oxidation product CO 2 at higher temperatures. Carbon monoxide binds strongly to Pd sites with NO and can delay NO release. A Pd/SSZ-13 washcoated monolith model developed in an earlier study [Ambast et al., Appl. Catal. B. Environmental (2021)] is upgraded to include C 12 H 26 storage, release, and conversion. Through a systematic combination of judicious experiments, model tuning, and validation, we provide evidence for the underlying NO uptake and release mechanisms in the presence of C 12 H 26 .

42 ENGINEERING↗
DOE OSTI2025

Cooperative and bifunctional Ga-Ca-Cr 2 O 3 @CaO structured monoliths as versatile platform for reactive capture of CO 2 and its subsequent conversion to ethylene

Cooperative and bifunctional materials (BFMs) that integrate adsorbents and catalysts offer a promising strategy for the reactive capture of CO 2 to produce valuable fuels and chemicals. In this study, we developed structured BFMs via 3D printing that combine CaO as an adsorbent with Ga–Ca–Cr 2 O 3 metal oxides as the catalyst for the reactive capture of CO 2 and its subsequent conversion to C 2 H 4 via the oxidative dehydrogenation of C 2 H 6 (CO 2 -ODHE). Three different Ga–Ca compositions were used to modify the catalyst surface characteristics and enhance C 2 H 4 selectivity. In these formulations, Ga ions stabilize the oxygen lattice of the BFM, while Ca ions interact strongly with Cr to form CaCrO 4 , thereby altering the oxygen species and enhancing the material’s basic properties. Under adsorption–reaction conditions at 600–650 °C, the optimal BFM achieved an excellent C 2 H 4 selectivity of 96.4 %, attributed to a balanced redox process and improved basicity that facilitate efficient C 2 H 6 conversion and rapid desorption of C 2 H 4 without excessive oxidation. Overall, this work provides new insights into the formulation of BFMs monoliths and highlights the critical role of catalytic surface modification in enhancing C 2 H 4 selectivity in the CO 2 -ODHE reactive capture process.

C2H4 production↗
DOE OSTI2015

Synthesis of Zn-MOF incorporating titanium-hydrides as active sites binding H{sub 2} molecules

This paper describes the synthetic effort for a Zn-MOF imparting Ti-H as a preferential binding site potentially capturing H{sub 2} molecules via Kubas-type interaction. The formation mechanism of Ti-H innate to the final material was potentially demonstrated to follow a radical dissociation rather than a β-hydrogen elimination and a C-H reductive elimination. - Graphical abstract: This study details the synthesis and the formation mechanism of Zn-MOF adsorbent site-isolating TiH{sub 3} that can potentially capture H{sub 2} molecules via Kubas-binding mechanism. - Highlights: • OH-functionalized Zn-MOF was employed as a reactive template to site-isolate TiH{sub 3}. • This MOF was post-synthetically modified using a tetracyclohexyl titanium (IV). • This intermediate was hydrogenolyzed to change ligand from cyclohexyl to hydride. • Formation mechanism of TiH{sub 3} was investigated via two control GC–MS experiments. • Final Zn-MOF potentially site-isolating TiH{sub 3} species was used as a H{sub 2} adsorbent.

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

o-Vanillin functionalized mesoporous silica – coated magnetite nanoparticles for efficient removal of Pb(II) from water

o-Vanillin functionalized mesoporous silica – coated magnetite (Fe{sub 3}O{sub 4}@MCM-41-N-oVan) was synthesized and fully characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, N{sub 2} adsorption–desorption technique and magnetic measurements. The capacity of Fe{sub 3}O{sub 4}@MCM-41-N-oVan to adsorb Pb(II) from aqueous solutions was evaluated in comparison with raw mesoporous silica – coated magnetite (Fe{sub 3}O{sub 4}@MCM-41) and amino – modified mesoporous silica coated magnetite (Fe{sub 3}O{sub 4}@MCM-41-NH{sub 2}). The effect of adsorption process parameters such us pH, contact time, initial Pb(II) concentration was also investigated. The adsorption data were successfully fitted with the Langmuir model, exhibiting a maximum adsorption capacity of 155.71 mg/g at pH=4.4 and T=298 K. The results revealed that the adsorption rate was very high at the beginning of the adsorption process, 80–90% of the total amount of Pb(II) being removed within the first 60 min, depending on the initial concentration. The results of the present work suggest that Fe{sub 3}O{sub 4}@MCM-41-N-oVan is a suitable candidate for the separation of Pb(II) from contaminated water. - Graphical abstract: A novel magnetic adsorbent based on o-vanillin functionalized mesoporous silica – coated magnetite was synthesized and fully characterized and its adsorption capacity for Pb(II) ions in aqueous solutions was evaluated. The maximum adsorption capacity for Pb(II) ions was determined to be 155.71 mg g{sup −1}. The adsorption rate was very high at the beginning of the adsorption process, 90% of the total amount of Pb(II) being removed within the first 60 min. Display Omitted.

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

High-performance magnetic carbon materials in dye removal from aqueous solutions

To obtain a novel adsorbent with excellent adsorption capacity and convenient magnetic separation property, magnetic activated semi-coke was prepared by KOH activation method and further modified by FeCl{sub 3}. The surface morphology, physical structure, chemical properties and textural characteristics of unmodified semi-coke, KOH-modified semi-coke and magnetic activated semi-coke were characterized by scanning electron microscopy, X-ray powder diffraction, N{sub 2} adsorption-desorption measurement, and electronic differential system. The adsorption characteristics of the magnetic activated semi-coke were explored for the removal of methyl orang (MO), methylene blue (MB), congo red (CR), acid fuchsin (AF), and rhodamine B (RB) from aqueous solution. The effects of adsorption parameters, including adsorbent dosage, pH and contact time, were investigated by comparing the adsorption properties of the magnetic activated semi-coke to RB. The result showed that the magnetic activated semi-coke displayed excellent dispersion, convenient separation and high adsorption capacity. The adsorption experiment data indicated that the pseudosecond order model and the Langmuir model could well explain the adsorption processes of RB on the magnetic activated semi-coke, and the maximum adsorption capacity (q{sub m}) was 526.32 mg/g. The values of thermodynamic parameters (ΔG°, ΔH° and ΔS°) indicated that the adsorption process depended on the temperature of the aqueous phase, and it was spontaneous and exothermic in nature. As the addition of the magnetic activated semi-coke, the color of the solution significantly faded. Subsequently, fast aggregation of the magnetic activated semi-coke from their homogeneous dispersion in the presence of an external magnetic field could be happened. So, the magnetic activated semi-coke displayed excellent dispersion, convenient separation and high adsorption capacity. - Graphical abstract: As the addition of the magnetic activated semi-coke, the color of the solution significantly faded. Subsequently, fast aggregation of the magnetic activated semi-coke from their homogeneous dispersion in the presence of an external magnetic field could be happened. So, the magnetic activated semi-coke displayed excellent dispersion, convenient separation and high adsorption capacity. Display Omitted.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2013

Phosphate adsorption on aluminum-coordinated functionalized macroporous–mesoporous silica: Surface structure and adsorption behavior

Graphical abstract: - Highlights: • Al-coordinated functionalized macroporous–mesoporous silica for phosphate removal. • It had the maximum adsorption capacity of 23.59 mg P/g. • Over 95% of the final adsorption capacity reached in the first 1 min. - Abstract: In this study, Al(III)-coordinated diamino-functionalized macroporous–mesoporous silica was synthesized and characterized by X-ray diffraction, N{sub 2} adsorption–desorption, Fourier transform infrared spectroscopy, scanning and transmission electron microscopy. Because of well-defined and interconnecting macroporous–mesoporous networks, the resulting adsorbent (MM-SBA) exhibited a significantly better phosphate adsorption performance and faster removal rate, as compared with the mesoporous adsorbent (M-SBA). Based on the Freundlich and Langmuir models, the phosphate adsorption capacity and the maximum adsorption capacity of MM-SBA were 7.99 mg P/g and 23.59 mg P/g, respectively. In the kinetic study of MM-SBA, over 95% of its final adsorption capacity reached in the first 1 min; whereas that of M-SBA was less than 79%.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Mussel-inspired surface modification of untreated wasted husks with stable polydopamine/polyethylenimine for efficient continuous Cr(VI) removal

Highlights: • Functional rice husks with abundant amino groups was firstly modified with PDA/PEI for Cr(VI) removal. • Potentiality of monolithic samples for dynamic continuous adsorption. • Expectable higher adsorption capacity than most of reported similar bio-sorbents. • Excellent mechanical stability, reusability and convenient separation. - Abstract: A cost-effective and chemically modified biological adsorbent based on agricultural wasted husks for heavy metal removal was fabricated by coating with Polydopamine–Polyethylenimine via the mussel inspired chemistry. Batch and fixed bed column adsorption experiments were carried out to explore the sorption capacity and potency of industrial application. The batch results indicated that the maximum adsorption capacity reached 42.8 mg/g which is much larger than most adsorbents based on bioresource and agricultural wastes for Cr(VI) removal in aqueous solution simultaneously with excellent recycling performance. In column adsorption experiments, it exhibited high mechanical stability and applied potential. The equilibrium time was 9130 min under the flow rate of 1 ml/min, and reached the equilibrium adsorption capacity of 47.14 mg/g. The breakthrough curves ploted by the data of fixed bed experiments under different flow rates (1 ml/min & 2 ml/min) fitted the Thomas model with R{sup 2} of 0.9510 and 0.9437 respectively.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2013

“Multi-temperature” method for high-pressure sorption measurements on moist shales

A simple and effective experimental approach has been developed and tested to study the temperature dependence of high-pressure methane sorption in moist organic-rich shales. This method, denoted as “multi-temperature” (short “multi-T”) method, enables measuring multiple isotherms at varying temperatures in a single run. The measurement of individual sorption isotherms at different temperatures takes place in a closed system ensuring that the moisture content remains constant. The multi-T method was successfully tested for methane sorption on an organic-rich shale sample. Excess sorption isotherms for methane were measured at pressures of up to 25 MPa and at temperatures of 318.1 K, 338.1 K, and 348.1 K on dry and moisture-equilibrated samples. The measured isotherms were parameterized with a 3-parameter Langmuir-based excess sorption function, from which thermodynamic sorption parameters (enthalpy and entropy of adsorption) were obtained. Using these, we show that by taking explicitly into account water vapor as molecular species in the gas phase with temperature-dependent water vapor pressure during the experiment, more meaningful results are obtained with respect to thermodynamical considerations. The proposed method can be applied to any adsorbent system (coals, shales, industrial adsorbents) and any supercritical gas (e.g., CH{sub 4}, CO{sub 2}) and is particularly suitable for sorption measurements using the manometric (volumetric) method.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2014

Modification of energy band alignment and electric properties of Pt/Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}/Pt thin-film ferroelectric varactors by Ag impurities at interfaces

We report on the effects of Ag impurities at interfaces of parallel-plate Pt/Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}/Pt thin film ferroelectric varactors. Ag impurities occur at the interfaces due to diffusion of Ag from colloidal silver paint used to attach the varactor samples with their back side to the plate heated at 600–750 °C during deposition of Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}. X-ray photoelectron spectroscopy and secondary ion mass spectrometry suggest that amount and distribution of Ag adsorbed at the interfaces depend strongly on the adsorbent surface layer. In particular, Ag preferentially accumulates on top of the Pt bottom electrode. The presence of Ag significantly reduces the barrier height between Pt and Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3} leading to an increased leakage current density and, thus, to a severe degradation of the varactor performance.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Design and Synthesis of Materials with High Capacities for Hydrogen Physisorption

Slit pore or planar geometries are the optimal morphology for adsorbents. Our initial effort was to explore single layer graphene as the ideal platform for adsorbents. As literature processes for graphene synthesis proved unreliable in generating structures of relevance, we concentrated our efforts on metal functionalization in order to enhance the normally modest 4-6 kJ/mole typical of carbons. The results of interest through this effort are the 32-36 g/l volume densities projected for 100 bar pressure for Cu modified material at 77K. Modest material compression would improve these values to densities comparable to 700 bar compressed gas tanks. Thermal Program Desorption (TPD) results from the same metal modified material showed hydrogen release over two temperature ranges. The initial range is 100 to 190 K from normally physisorbed gas while chemisorbed hydrogen from the Cu surface showed desorption starting at 300 K. This work suggests a pathway toward higher temperature utility based on both physisorption and chemisorption phenomena. Chemisorption was validated by observing isotope exchange with deuterium.

08 HYDROGEN↗
DOE OSTI2021

Development of Passive HC/NOx Trap Catalysts for Low Temperature Gasoline Applications

This project aimed to develop fundamental understanding of the chemistry of NO adsorption and reaction in Pd/zeolites so as to facilitate the rational design of passive NOx adsorber catalysts. The approach adopted combined both experimental and computational methods, which together allow a deeper understanding of the governing chemistry than the use of either method alone. The workflow began with Pd/H-CHA and Pd/H-BEA catalyst synthesis and characterization, in which the Si/Al ratio and Al siting were systematically varied. This was followed by catalyst evaluation using temperature-programed adsorption/desorption methods, as well as in situ spectroscopic measurements to probe the chemistry of NO adsorption. In parallel, the adsorption of NO and other relevant species (H 2 O, CO, HCs) was studied by means of quantum chemical calculations in order to rationalize the experimental data and provide additional insights. Catalyst aging studies were also performed with the aim of elucidating the mechanism of catalyst degradation. Finally, the insights gained in this project were applied to the preparation of an optimized HC/NOx adsorber catalyst, the performance of which was studied using exhaust gas from an engine dynamometer.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
NASA NTRS2019

Dynamic Modeling of Gaseous Multicomponent Trace Contaminant Adsorption

Activated carbon is a porous material in the Trace Contaminant Control (TCC) system that physically adsorbs volatile organic compounds (VOCs) generated within spacecraft and spacesuit environments. Several isotherm models exist to predict adsorption equilibria for processes involving multicomponent systems. This paper investigates the use of Ideal Adsorbed Solution Theory (IAST) for predicting multicomponent trace contaminant adsorption behavior using single-component isotherms based on potential theory. Developing simulations for experimental breakthrough curves will gauge the validity on the sizing and design of TCC architecture. Model results on predicting bed performance and roll-up effects are compared with available multicomponent test data.

Ideal Adsorbed Solution Theory (IAST)↗
DOE OSTI2013

Activities for the remediation of TEPCO's Fukushima Daiichi nuclear power plant

With the aim of fulfilling recovery work for the Fukushima Daiichi NPP, technological efforts have been made for the development of a survey robot system, adequate communication infrastructure technologies, high radiation environment compatible gamma cameras, heavy machinery-type robots (ASTACO-SoRa), remote decontamination devices (AROUNDER), and contaminated waste water treatment system. We have developed a new type of absorbents which remove cesium (Cs) and strontium (Sr) simultaneously at a high removal rate of 99 % or more. We will provide valuable solutions and rational systems for waste water treatment using this developed adsorbent as well as other various adsorbents for the recovery of Fukushima Daiichi NPP.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2015

Decontamination of organic wastes containing radionuclides - 15122

The Arvia Process is being adapted for use in the nuclear industry for the decontamination of oils containing radionuclides. This waste treatment process uses adsorption followed by electrochemical oxidation as an alternative technique to conventional incineration. A study has been carried out on components of the Arvia Process with the aim of understanding the changes in chemistry due to ionizing radiation. Samples of adsorbent in water have been exposed to gamma-rays from a Co-60 irradiator at absorbed doses of 3, 19, and 304 kGy. Preliminary results show that the concentration of inorganic ions and carbon in the water increased as a function of dose. This increase suggests that degradation of the adsorbent may take place at high doses. Further characterization of the microstructure and adsorption studies post-irradiation are planned. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Arvia organics destruction: an innovative treatment approach for dioxins, furans and other problematic (Orphan) organic wastes - 15380

The safe and efficient disposal of radionuclide-contaminated organic wastes is a key component in the life-cycle of a nuclear power plant. Technologies are available for the processing of some of these wastes although there are a number of waste streams for which the disposition path is not clear or does not exist at all. For example, waste streams such as dioxin, furan and PCB-laden oils pose an issue for the US Dept. of Energy complex. These wastes present a challenge as they cannot be readily treated using existing treatment technologies because of legislative and material constraints such as gaseous phase radioactivity discharge limits, waste elemental content, by-product generation and waste resistance to thermal decomposition. Alternate methods of organics destruction can circumvent some of these issues by using different mechanisms of organics oxidation. One such innovative method, known as the Arvia organics destruction process, combines adsorption with electrochemical combustion and offers such an alternative. This technology, based on a patented material, Nyex{sup TM} that is able to act as both an adsorbent and as an electrode, allows the electrochemical combustion of adsorbed organics to occur on the material's surface. The result is the destruction of organics whilst the bulk of inorganic and radionuclide components remain in the aqueous phase. These components can subsequently be treated using existing waste processing technologies. This paper outlines recent work conducted on demonstrating the Arvia process against the destruction of dioxin, furan and PCB-laden wastes that demonstrates that the technology successfully removes these target species to below discharge standards in the aqueous phase. Based on these successful trials a test unit has been designed to demonstrate the process on actual radioactive wastes at the DOE Oak Ridge facility. The successful treatment of F027-coded waste has also been demonstrated and will be reported. The above work showcases the development, scaling and application of an innovative technology, first presented to the industry at the Waste Management Symposia in 2012, as another option for the treatment of challenging wastes with expensive, complex or no current disposal routes. The Arvia process adds to the portfolio of available treatment technologies and will help facilitate the decommissioning and waste disposal responsibilities of the nuclear industry. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Bio-sorption of thorium by bone meal - 15435

In the recent years, there is an increasing interest in the application of biological materials for the removal of heavy metal ions from aqueous solutions. There are a variety of biological materials that have been proven efficient bio-sorbents such as agriculture residues, plants, algae, etc. The use of these materials is attractive and advantageous because they are inexpensive in comparison with commercial adsorbents. Bone meal is a biological material that reunites low cost and efficiency. It is a natural material that contains large amount of calcium phosphate in the form of hydroxyapatite. Studies with hydroxyapatite showed that this material is efficient in removing heavy metals from polluted soils due to their ability to adsorb molecules and can be used to remove radionuclides from liquid aqueous solutions, as liquid radioactive wastes generated in many activities. Bone meal was purchased in local market and chopped and sieved to obtain particle size between 0.297 mm and 0.125 mm. Batch bio-sorption experiments were performed to determine the metal uptake capacity and equilibrium time. Fixed concentrations of thorium solutions were prepared by dissolving thorium nitrate in distillate water. The bone meal was suspended in 5 mL of thorium solutions in a ratio of 0.2% w/v and left in contact during different times. The contact times adopted were 30 min, 1, 2 and 4 hours. After the contact time, the bone meal was removed by filtration and the supernatant, analyzed by inductively coupled plasma optical emission spectrometry (ICP-OES). The results were evaluated using isotherms and kinetics models. The maximum capacity for the bone meal was 11.5 mg/g in 2 h. These results suggest that bio-sorption with bone meal can be applied in the treatment of aqueous solutions and liquid radioactive wastes containing thorium. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Capture of volatile fission products: present status and future perspectives - 15680

The performance of some adsorbent materials for retention of volatile fission products has been assessed. Two different zeolites (Zeolite 4A and silver-coated mordenite) have been chosen owing to their known capacity to entrap cesium and iodine, respectively. To this purpose experiments have been made with a pilot plant termed OGATA (Off-Gas Treatment Apparatus), installed at ENEA laboratories. The tests have been carried out by heating the volatile species at 900 deg. C and passing them through zeolite pellets with the help of argon as carrier gas. The products arising from the interaction with the zeolites have been analyzed mainly by X-rays diffractometry and scanning electron microscopy. The general conclusion from these experiments is that the retention of volatile elements, like cesium and iodine, occurs through a simple adsorption mechanism, which confirms the need to improve the trapping capacity of these materials, especially in view of the final disposal. Moreover, a metal-organic framework (MOF-5), as representative of the new class of materials proposed as adsorbents for volatile radionuclides has been taken into account. The metal-organic frameworks are a sub-family of the nano-porous crystals, characterized by metal-oxygen cages connected by organic bridges which currently attract intensive interest for their excellent potential for storing and separating gases. The synthesis of MOF-5 has been made according to a novel method reported in the literature. FTIR, XRD and Raman spectra, as well as SEM-EDS and thermal gravimetric analysis performed on the synthesized product are perfectly in agreement with current data and reveal the crystal structure of the MOF-5. (authors)

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗