Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “Ca”

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 343 records · Page 19

Combined Theoretical Analysis of the Parity-Violating Asymmetry for 48 Ca and 208 Pb

The recent experimental determination of the parity violating asymmetry A PV in 48 Ca and 208 Pb at Jefferson Lab is important for our understanding on how neutrons and protons arrange themselves inside the atomic nucleus. To better understand the impact of these measurements, we present a rigorous theoretical investigation of A PV in 48 Ca and 208 Pb and assess the associated uncertainties. Here, we complement our study by inspecting the static electric dipole polarizability in these nuclei. The analysis is carried out within nuclear energy density functional theory with quantified input. We conclude that the simultaneous accurate description of A PV in 48 Ca and 208 Pb cannot be achieved by our models that accommodate a pool of global nuclear properties, such as masses and charge radii, throughout the nuclear chart, and describe—within one standard deviation—the experimental dipole polarizabilities in these nuclei.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Iridium valence variation and carrier sign tuning in ( Ca , Ba ) x La 2 – x CuIrO 6 double perovskites

Here, we report the structure and properties of ( Ca , Ba ) x La 2 – x CuIrO 6 . The rock-salt double perovskite structure goes through a P 1 ¯ to P 2 1 / n phase transition with increasing Ba content but not with Ca content. In both cases, the Ir ion is oxidized from 4 + to 5 + with increasing substitution. Transport and magnetic properties measurements reveal that all compositions are insulating with hysteretic spin-freezing magnetic behavior. Seebeck coefficient measurements reveal a large thermopower change from + 176 μ V /K in La 2 CuIrO 6 to – 223 μ V /K with increasing Ba content in Ba x La 2 – x CuIrO 6 . This behavior is modeled well by the Heikes formula for correlated hopping conduction. ( Ca , Ba ) x La 2 – x CuIrO 6 provides a model system for investigations of other systems with similar carrier sign tuning, with applications toward semiconductors and thermoelectric materials.

36 MATERIALS SCIENCE↗

Metadynamics simulations reveal mechanisms of Na + and Ca 2+ transport in two open states of the channelrhodopsin chimera, C1C2

Cation conducting channelrhodopsins (ChRs) are a popular tool used in optogenetics to control the activity of excitable cells and tissues using light. ChRs with altered ion selectivity are in high demand for use in different cell types and for other specialized applications. However, a detailed mechanism of ion permeation in ChRs is not fully resolved. Here, we use complementary experimental and computational methods to uncover the mechanisms of cation transport and valence selectivity through the channelrhodopsin chimera, C1C2, in the high- and low-conducting open states. Electrophysiology measurements identified a single-residue substitution within the central gate, N297D, that increased Ca 2+ permeability vs. Na + by nearly two-fold at peak current, but less so at stationary current. We then developed molecular models of dimeric wild-type C1C2 and N297D mutant channels in both open states and calculated the PMF profiles for Na + and Ca 2+ permeation through each protein using well-tempered/multiple-walker metadynamics. Results of these studies agree well with experimental measurements and demonstrate that the pore entrance on the extracellular side differs from original predictions and is actually located in a gap between helices I and II. Cation transport occurs via a relay mechanism where cations are passed between flexible carboxylate sidechains lining the full length of the pore by sidechain swinging, like a monkey swinging on vines. In the mutant channel, residue D297 enhances Ca 2+ permeability by mediating the handoff between the central and cytosolic binding sites via direct coordination and sidechain swinging. We also found that altered cation binding affinities at both the extracellular entrance and central binding sites underly the distinct transport properties of the low-conducting open state. This work significantly advances our understanding of ion selectivity and permeation in cation channelrhodopsins and provides the insights needed for successful development of new ion-selective optogenetic tools.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

AmeriFlux FLUXNET-1F CA-DB2 Delta Burns Bog 2

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site CA-DB2 Delta Burns Bog 2. This is the FLUXNET version of the carbon flux data for the site CA-DB2 Delta Burns Bog 2 produced by applying the standard ONEFlux (1F) software. Site Description - The Burns Bog Ecological Conservancy Area (BBECA) in the metro Vancouver area presents a unique opportunity for insight into greenhouse gas dynamics post restoration. The bog was significantly disturbed for peat mining, development and agriculture over the last century, however since 2005 there has been both active restoration and natural regeneration occurring within the bog. Hence areas of bog are at varying stages of ecological recovery. This site is a Pine-Sphagnum low shrub site characteristic of a later successional stage. Conversely, CA-DBB, another AmeriFlux site in BBECA, is a Beakrush-Sphagnum site characteristic of an earlier successional stage.

Knox, Sara↗

AmeriFlux FLUXNET-1F CA-SCC Scotty Creek Landscape

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site CA-SCC Scotty Creek Landscape. This is the FLUXNET version of the carbon flux data for the site CA-SCC Scotty Creek Landscape produced by applying the standard ONEFlux (1F) software. Site Description - The Scotty Creek flux tower is located in an organic-rich boreal forest-wetland landscape about 50 km south of Fort Simpson in the Taiga Plains of the Mackenzie watershed. The tower was installed in 2013 and operates an open-path EC system year-round running on solar power only. Flux footprints contain about 50 % forested peat plateaus and 50 % wetlands (i.e., collapse-scar bogs). The forests are underlain by permafrost, while the treeless wetlands are permafrost-free. The tower itself is located on a forested peat plateau. Black spruce tree density on plateaus is sparse and the mean canopy height is ca. 5 m.

Sonnentag, Oliver↗

Uranium (VI) Adsorbate Structures on Portlandite [Ca(OH)2] Type Surfaces Determined by Computational Modelling and X-ray Absorption Spectroscopy

Portlandite [Ca(OH) 2 ] is a potentially dominant solid phase in the high pH fluids expected within the cementitious engineered barriers of Geological Disposal Facilities (GDF). This study combined X-ray Absorption Spectroscopy with computational modelling in order to provide atomic-scale data which improves our understanding of how a critically important radionuclide (U) will be adsorbed onto this phase under conditions relevant to a GDF environment. Such data are fundamental for predicting radionuclide mass transfer. Surface coordination chemistry and speciation of uranium with portlandite [Ca(OH) 2 ] under alkaline groundwater conditions (ca. pH 12) were determined by both in situ and ex situ grazing incidence extended X-ray absorption fine structure analysis (EXAFS) and by computational modelling at the atomic level. Free energies of sorption of aqueous uranyl hydroxides, [UO 2 (OH) n ] 2–n (n = 0–5) with the (001), (100) and (203) or (101) surfaces of portlandite are predicted from the potential of mean force using classical molecular umbrella sampling simulation methods and the structural interactions are further explored using fully periodic density functional theory computations. Although uranyl is predicted to only weakly adsorb to the (001) and (100) clean surfaces, there should be significantly stronger interactions with the (203/101) surface or at hydroxyl vacancies, both prevalent under groundwater conditions. The uranyl surface complex is typically found to include four equatorially coordinated hydroxyl ligands, forming an inner-sphere sorbate by direct interaction of a uranyl oxygen with surface calcium ions in both the (001) and (203/101) cases. In contrast, on the (100) surface, uranyl is sorbed with its axis more parallel to the surface plane. The EXAFS data are largely consistent with a surface structural layer or film similar to calcium uranate, but also show distinct uranyl characteristics, with the uranyl ion exhibiting the classic dioxygenyl oxygens at 1.8 Å and between four and five equatorial oxygen atoms at distances between 2.28 and 2.35 Å from the central U absorber. These experimental data are wholly consistent with the adsorbate configuration predicted by the computational models. These findings suggest that, under the strongly alkaline conditions of a cementitious backfill engineered barrier, there would be significant uptake of uranyl by portlandite to inhibit the mobility of U(VI) from the near field of a geological disposal facility.

36 MATERIALS SCIENCE↗

Electronic structure of Ca, Sr, and Ba under pressure.

Electronic band structure calculations phase of Ca, Sr and Ba over wide range of atomic volumes under pressure electronic band structure calculations for fcc phase of Ca, Sr and Ba over wide range of atomic volumes under pressure electronic band structure calculations for fcc phase of Ca, Sr and Ba over wide range of atomic volumes under pressure

BARIUM↗

Mineralogy of lunar norite 78235 - Second lunar occurrence of P2 sub 1 ca pyroxene from Apollo 17 soils

A thin section of lunar rock 78235 is examined optically as well as with an electron microprobe and is shown to be a highly-shocked coarse norite. The rock is found to consist of approximately 30% low-Ca pyroxene, 55% Ca-rich plagioclase, and 15% glass veins. The composition of the glass veins is analyzed, and it is suggested that they resulted from shock melting of the norite. Comparisons with other noritic rocks indicate that the pyroxene in rock 78235 has P2 sub 1 ca symmetry. Based on this symmetry plus the coarse grain size, it is concluded that rock 78235 was formed under plutonic conditions. The origin of the minor phases in this rock is briefly considered.

Steele, I. M.↗

Observations of the Ca/+/ twilight airglow from intermediate layers of ionization

Optical and incoherent scatter radar techniques are applied to detect the presence of Ca(+) in lower thermospheric intermediate layers over Arecibo. The Arecibo 430 MHz radar is used to measure electron densities, and the altitude distribution and density of the calcium ion is inferred from the variation of twilight resonant scattering with solar depression angle. Ca(+) and electron column densities are compared, and results indicate that the composition of low-altitude intermediate layers is 2% Ca(+), which is consistent with rocket mass spectrometer measurements. Fe(+) and Mg(+) ultraviolet resonance lines are not detected from the ground due to ozone absorbing all radiation short of 3000 A, and measurements of the neutral iron resonance line at 3860 A show that an atmospheric continuum may result in overestimations of emission rates at high solar depression angles.

Tepley, C. A.↗

IUE observations of pre-main-sequence stars. I - Mg II and Ca II resonance line fluxes for T Tauri stars

IUE satellite and Lick 3 m reflector image tube scanner measurements of the Mg II and Ca II resonance lines in a sample of T Tauri stars are the basis of a discussion of the Mg II h and k line emission and the Ca II H and K line emission, within the context of stellar chromospheres. Corroborative evidence is presented for the chromospheric origin of these resonance lines, and chromospheric radiative loss rates in the Mg II and Ca II resonance lines are derived. It is found that the degree of nonradiative heating present in the outer atmospheres of T Tauri stars generally exceeds that of the RS CVn systems, as well as the dMe stars and other active chromospheric dwarfs, and it is inferred that the surfaces of such pre-main sequence stars are covered by regions similar to solar plages. The mean chromospheric electron density of T Tauri stars is determined as 10 to the 11th/cu cm.

Giampapa n, M. S.↗

In vitro Ca-45/++/ uptake and exchange by otoconial complexes in high and low K/+/Na/+/ fluids

Recently, data have been accumulating to indicate that saccular and utricular otoconial complexes of the gravity receptor organs are dynamic and interact constantly with their environment. This study investigates the possibility that the ionic composition of the surrounding fluid influences calcium ion binding and release, and explores the importance of the K(+)/Na(+) ratio. Two in-vitro methods were developed, the first of which employed artificial endolymph and perilymph while ionically balanced fluids in which only the K(+)/Na(+) was altered were used in the second. The ability of rat complexes to take up Ca-45(++) during incubation with these fluids was assessed using liquid scintillation spectrometry. In vitro uptake of Ca-45(++) was greater in fluids with a high K(+)/Na(+) ratio than in fluids in which the ratio was low. The ability of the complexes to take up Ca-45(++) appeared to decline with age.

Ross, M. D.↗

Lunar highland rocks - Element partitioning among minerals. II - Electron microprobe analyses of Al, P, Ca, Ti, Cr, Mn and Fe in olivine

Lunar olivines from anorthosites, granulitic impactites, and rocks in the Mg-rich plutonic trend were subjected to electron probe measurements for Al, P, Ca, Ti, Cr and Mn, which show that the FeO/MnO ratio for lunar olivines lies between 80 and 110 with little difference among the rock types. The low values of Ca in lunar olivines indicate slow cooling to subsolidus temperatures, with blocking temperatures of about 750 C for 67667 and 1000 C for 60255,73-alpha determined by the Finnerty and Boyd (1978) experiments. An important paradox is noted in the low Ti content of Fe-rich olivines from anorthosites, although both Ti and Fe tend to become enriched in liquid during fractional distillation. Except for Ca and Mn, olivine from anorthosites has lower minor element values than other rock types. Formation from a chemically distinct system is therefore implied.

Smith, J. V.↗

X-ray observations of the southern cluster CA 0340-538 and the Horologium supercluster

X-ray observations of the Horologium supercluster are examined. Results show that the optically Coma-like cluster CA 0340-538 has a smooth X-ray structure which also resembles that of Coma. The density structure of its X-ray emitting gas, determined in a model-independent way, is found to be remarkably featureless, being consistent with a nearly isothermal polytrope out to approximately 2 Mpc from the cluster center. The total mass of the gas is determined to exceed 10% of the cluster virial mass and may contribute a substantial fraction of the cluster binding mass. Although CA 0329-527 is found to be an X-ray double cluster, its structure appears to be confused. CA 0325-539 is found to show no substantial X-ray emission. An upper limit of 1.3 x 10 to the 44th erg/s is determined for any diffuse 2-10 keV emission from the Horologium supercluster.

Ku, W. H.-M.↗

Electron microprobe analyses of Ca, S, Mg and P distribution in incisors of Spacelab-3 rats

The distribution of Ca, S, Mg and P was mapped within the incisors of Spacelab-3 rats using an electron microprobe. The data indicate that Flight rats maintained in orbit for 7 days have significantly higher Ca/Mg ratios in dentin due to both higher Ca and lower Mg content than in dentin of ground-based Controls. There is no statistical difference in distribution of either P or S within Fligth animals and Controls, but there is clear indication that, for P at least, the reason is the greater variability of the Control data. These results are consistent with those obtained on a previous NASA/COSMOS flight of 18.5 days duration, although they are not pronounced. The results further suggest that continuously growing rat incisors provide useful records of the effects of weightlessness on Ca metabolism.

Rosenberg, G. D.↗

Temperature and composition dependencies of trace element partitioning - Olivine/melt and low-Ca pyroxene/melt

This paper presents a systematic thermodynamic analysis of the effects of temperature and composition on olivine/melt and low-Ca pyroxene/melt partitioning. Experiments were conducted in several synthetic basalts with a wide range of Fe/Mg, determining partition coefficients for Eu, Ca, Mn, Fe, Ni, Sm, Cd, Y, Yb, Sc, Al, Zr, and Ti and modeling accurately the changes in free energy for trace element exchange between crystal and melt as functions of the trace element size and charge. On the basis of this model, partition coefficients for olivine/melt and low-Ca pyroxene/melt can be predicted for a wide range of elements over a variety of basaltic bulk compositions and temperatures. Moreover, variations in partition coeffeicients during crystallization or melting can be modeled on the basis of changes in temperature and major element chemistry.

Colson, R. O.↗

Integrated-light spectroscopy of globular clusters at the infrared Ca II lines

Integrated-light spectroscopy has been obtained for 27 globular clusters at the Ca II IR triplet. Line strengths and radial velocities have been measured from the spectra. For the well-studied clusters in the sample, the strength of the Ca II lines is very well correlated with previous metallicity estimates. Thus, the triplet is useful as a metallicity indicator in globular cluster integrated-light spectra. The greatly reduced effect of interstellar extinction at these wavelengths (compared to the blue region of the spectrum) has permitted observations of some of the most heavily reddened clusters in the Galaxy. For several such clusters, the Ca II triplet metallicities are in poor agreement with metallicity estimates from IR photometry by Malkan (1981). The strength of an interstellar band at 8621A has been used to estimate the amount of extinction towards these clusters. Using the new metallicity and radial-velocity data, the metallicity distribution, kinematics, and spatial distribution of the disk globular cluster system have been analyzed. Results very similar to those of Zinn (1985) have been found. The relation of the disk globulars to the stellar thick disk is discussed.

Armandroff, Taft E.↗

The magnetic, basal, and radiative-equilibrium components in Mount Wilson Ca II H + K fluxes

Mount Wilson Ca II H + K flux measurements of cool dwarf stars are analyzed and compared with stellar Mg II h + k fluxes, variability amplitudes, rotation rates, and solar data. It is concluded that the Mount Wilson Ca II H + K fluxes comprise three principal parts: (1) a photospheric contribution in the line wings, (2) a basal chromospheric component that appears to be unrelated to stellar magnetic activity and is, therefore, possibly nonmagnetic in origin, and (3) a chromospheric component which is associated with magnetically active regions and the (quiet and active) network. The basal chromosphere appears to cover the entire surface of magnetically inactive stars. The basal Ca II H + K flux density for solar-type stars equals the average emission observed in the centers of solar supergranulation cells, where the magnetic flux density is small.

Schrijver, C. J.↗

PHL 1226 and IC 1746 - A QSO-galaxy pair without Ca II or Na I absorption

Spectroscopic observations of the QSO PHL 1226 show no absorption lines at the expected wavelengths of Ca II H and K and Na I D absorption at the redshift of the nearby galaxy IC 1746 (z = 0.0176). The line of sight to PHL 1226 intercepts IC 1746 near the galaxy major axis at a projected separation from the galaxy nucleus of 28/h50 kpc. The 3-sigma upper limits on equivalent width attained in the spectra are 110 mA for Ca II H or K and 90 mA for either of the Na I D lines. The probable Ca II K line reported by Bergeron et al. (1988) is not confirmed.

Junkkarinen, Vesa T.↗