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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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Rate and Selectivity Control in Thioether and Alkene Oxidation with H 2 O 2 over Phosphonate-Modified Niobium(V)-Silica Catalysts
Supported metal oxide catalysts are versatile materials for liquid-phase oxidations, including alkene epoxidation and thioether sulfoxidation with H2O2. Periodic trends in H2O2 activation was recently demonstrated for alkene epoxidation, highlighting Nb-SiO2 as a more active and selective catalyst than Ti-SiO2. Three representative catalysts are studied consisting of NbV, TiIV, and ZrIV on silica, each made through a molecular precursor approach that yields highly dispersed oxide sites, for thioanisole oxidation by H2O2. Initial rates trend Nb>Ti>>Zr, as for epoxidation, and Nb outperforms Ti for a number of other thioethers. In contrast, selectivity to sulfoxide vs. sulfone trends Ti>Nb>>Zr at all conversions. Modifying the Nb-SiO2 catalyst with phenylphosphonic acid does not completely remove sulfoxidation reactivity, as it did for photooxidation and epoxidation, and results in an unusual material active for sulfoxidation but neither epoxidation nor overoxidation to the sulfone.
Controlling Porosity in Lignin‐Derived Nanoporous Carbon for Supercapacitor Applications
Abstract Invited for this month′s cover is a group of collaborators led by Satish Nune at Pacific Northwest National Laboratory. The image shows the path to renewable energy storage using high surface area carbons derived from low‐cost renewable lignin. The Communication itself is available at 10.1002/cssc.201402621 .
Simulation and 4D seismic studies of pressure management and CO 2 plume control by means of brine extraction and monitoring at the Devine Test Site, South Texas, USA: Original Research Article: Simulation and 4D seismic studies of pressure management and CO 2 plume control
Not provided.
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.
An allosteric model for control of pore opening by substrate binding in the EutL microcompartment shell protein
Abstract not provided
Ultrafast study of phonon transport in isotopically controlled semiconductor nanostructures: Phonons in isotopically controlled multilayers
Isotopically modulated silicon and germanium multilayers are analyzed by means of femtosecond spectroscopy and pulsed X-ray scattering for determining thermal conductivity and phonon modes. Isotopic modulation decreases thermal conductivity stronger than expected from a band bending model in the coherent phonon transport regime, in particular for silicon. Femtosecond spectroscopy and X-ray scattering resolve zone-folded vibration modes, which are located at the edge of the new, smaller Brillouin zone due to the multilayer periodicity. These modes can contribute to the reduction of thermal conductivity by Umklapp processes within the zone-folded mini-bands. Color-coded increase in ultrafast X-ray scattering in vicinity to the mini-zone boundary of a germanium multilayer.
Planetary and synoptic-scale dynamic control of extreme cold wave patterns over the United States
Not Available
Metrics for understanding large-scale controls of multivariate temperature and precipitation variability
Not Available
Valuing the Ozone-Related Health Benefits of Methane Emission Controls
Methane is a greenhouse gas that oxidizes to form ground-level ozone, itself a greenhouse gas and a health-harmful air pollutant. Reducing methane emissions will both slow anthropogenic climate change and reduce ozone-related mortality. We estimate the benefits of reducing methane emissions anywhere in the world for ozone-related premature mortality globally and for eight geographic regions. Our methods are consistent with those used by the U.S. Government to estimate the Social Cost of Carbon (SCC). We find that the global short- and long-term premature mortality benefits due to reduced ozone production from methane mitigation are (2011)$790 and $1775 per tonne methane, respectively. These correspond to approximately 70% and 150% of the valuation of methane’s global climate impacts using the SCC after extrapolating from carbon dioxide to methane using Global Warming Potential (GWP) estimates. Results are most sensitive to the choice of VSL and increase for emission years further in the future. Regionally, most of the global mortality benefits accrue in Asia, but 10% accrue in the United States. This methodology can be used to assess the benefits of methane emission reductions anywhere in the world, including those achieved by national and multinational policies.
Controlled Generation of TiO x –Au Interface Using Titanium Molecular Complex Bearing Pyridyl Anchors: Synthesis, Characterization and Catalysis
Interfacial perimeter sites between metal and support are often important for catalysis. A mononuclear titanium siloxy complex III, Ti(acac) 2 [OSiC 6 H 5 N(OCH 3 ) 2 ] 2 was synthesized to generate TiOx units of different degrees of clustering to decorate Au nanoparticles. Two different methods of preparation were examined; one was to deposit III onto Au/SiO 2 and the other was to form III-covered Au nanoparticle first before deposition onto SiO 2 . The former method generated more highly dispersed TiO x units, while larger domains of TiO 2 were formed with the latter method, as deduced by UV–vis and XAS characterization. A model was proposed to explain how TiO x dispersity could be related to the preparative procedures. These samples were further tested as catalysts in selective oxidation of propane in a stream of O 2 and H 2 . They exhibited different product selectivities. The sample with more dispersed TiO x units were more selective for acetone formation versus propene formation. The results confirmed the important role of both the Au–TiO x interface at the perimeter and the extent of Ti isolation in the TiO x phase in the reaction.
Design and Evaluation of SunSpec-Compliant Smart Grid Controller with an Automated Hardware-in-the-Loop Testbed.
Abstract not provided.
A General Framework for Sensitivity-Based Optimal Control and State Estimation.
Abstract not provided.
Optimal estimation and scheduling in aquifer management using the rapid feedback control method
Not Available