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At least 91 records · Page 5

Shell model analysis of the B ( E 2,2 + → 0 + ) values in the A = 70, T = 1 triplet 70 Kr, 70 Br, and 70 Se

The B(E2, 2 + → 0 + ) transition strengths of the T=1 isobaric triplet 70 Kr, 70 Br, 70 Se, recently measured at the RIKEN Radioactive Isotope Beam Factory (RIBF), are discussed in terms of state-of-the-art large scale shell model calculations using the JUN45 and JUN45 + LNPS plus Coulomb interactions. In this Letter we argue that, depending on the effective charges used, the calculations are either in line with the experimental data within statistical uncertainties, or the anomaly happens in 70 Br, rather than 70 Kr. In the latter case, we suggest that it can be due to the presence of a hitherto undetected 1 + T = 0 state below the yrast 2 + T = 1 state. Furthermore, our results do not support a shape change of 70 Kr with respect to the other members of the isobaric multiplet.

59 ≤ A ≤ 89↗

Proton removal from Br 73 , 75 to Se 72 , 74 at intermediate energies

Herein we report new experimental data for excited states of 72,74 Se obtained from proton removal from 73,75 Br secondary beams on a proton target. The experiments were performed with the Ursinus-NSCL Liquid Hydrogen Target and the combined GRETINA+S800 setup at the Coupled Cyclotron Facility of the National Superconducting Cyclotron Laboratory at Michigan State University. Within uncertainties, the inclusive cross sections for proton removal from 73,75 Br on a proton target are identical suggesting that the same single-particle orbitals contribute to the proton-removal reaction. In addition, details of the partial cross section fragmentation are discussed. The data might suggest that l = 1, 2, 3, and 4 angular momentum transfers are important to understand the population of excited states of 72,74 Se in proton removal. Available data for excited states of 74 Ge populated through the 75 As(d, 3 He) 74 Ge proton-removal reaction in normal kinematics suggest indeed that the fp and sd shell as well as the 1g 9/2 orbital contribute. A comparison to data available for odd-A nuclei supports that the bulk of the spectroscopic strengths could be found at lower energies in the even-even Se isotopes than in, for instance, the even-even Ge isotopes. In addition, the population of high-J states seems to indicate that multi-step processes contribute to proton-removal reactions at intermediate energies in these collective nuclei.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Li 7 P 2 S 8 Br 0.5 I 0.5 (LPSBI) solid state electrolyte by XPS

There have been increasing surface characterization studies of battery materials specifically in the context of before and after cell operation to determine any chemical changes. Therefore, providing reliable reference spectra of battery-related materials is important. In this paper, survey and high-energy resolution data are reported for the solid-state electrolyte Li 7 P 2 S 8 Br 0.5 I 0.5 (LPSBI), which has been synthesized and characterized at Pacific Northwest National Laboratory. The current data presents narrow scan regions of I 3d, I 4d, Br 3d, O 1s, P 2p, S 2p, and C 1s core level spectra as well as wide-scan survey data that was obtained using Al K a x-ray source with a Thermo Fisher Nexsa instrument.

25 ENERGY STORAGE↗

E-Field_Log Metadata, BR-Ma2: Manaus, 2016 - 2017

This data package contains the Excel file "E-Field_Log_v1-1_BR-Ma2_20190725_20190910175444," which has metadata for sap velocity, leaf temperature, leaf gas exchange, and soil water content data packages. Each data package is listed in the below field "dataset references." All data was collected from the NGEE Tropics site in Manaus, Brazil (BR-Ma2), between 24 May 2016 and 16 March 2017. This dataset replaces the E-Field metadata file of two retired packages, NGT0019 and NGT0040. This metadata file includes site details, species information, equipment used, and more. For more information about the design and use of the E-Field_Log and accompanying metadata files, see Danielle Christianson, Charuleka Varadharajan, Brad Christoffersen, Matteo Detto, Boris Faybishenko, Val Hendrix, Kolby Jardine, Robinson Negron-Juarez, Bruno Gimenez, Gilberto Pastorello, Thomas Powell, Megha Sandesh, Jeffrey Warren, Brett Wolfe, Jeff Chambers, Lara Kueppers, Nate McDowell, Deb Agarwal(2018). FRAMES Metadata Reporting Templates for Ecohydrological Observations, version 1.1. NGEE Tropics Data Collection. Accessed at http://dx.doi.org/10.15486/ngt/1419956.

54 ENVIRONMENTAL SCIENCES↗

AmeriFlux FLUXNET-1F BR-Npw Northern Pantanal Wetland

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site BR-Npw Northern Pantanal Wetland. This is the FLUXNET version of the carbon flux data for the site BR-Npw Northern Pantanal Wetland produced by applying the standard ONEFlux (1F) software. Site Description - The site is located in the northern Pantanal in central South America. The site is subject to seasonal flooding with distinct wet seasons (November to April) and dry seasons (May to October).

Vourlitis, George↗

AmeriFlux FLUXNET-1F BR-CST Caatinga Serra Talhada

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site BR-CST Caatinga Serra Talhada. This is the FLUXNET version of the carbon flux data for the site BR-CST Caatinga Serra Talhada produced by applying the standard ONEFlux (1F) software. Site Description - This tower is located in a seasonal tropical dry forest (caatinga) in the semi-arid region of Brazil. There is no wood extraction for at least 50 years, and because it is an open area, there is cattle grazing during the wet season.

Antonino, Antonio↗

AmeriFlux BR-Ji3 Ji-Paraná/RO - Reserva Biológica do Jaru (RBJ)

This is the AmeriFlux version of the carbon flux data for the site BR-Ji3 Ji-Paraná/RO - Reserva Biológica do Jaru (RBJ). Site Description - The BR-Ji3, RBJ tower (LBA Network) is deployed in a primary forest in the Reserva Biologica do Jaru, management to ICMBio, at 130 km of Ji-Paraná city, in the road to Vale do Paraíso.

Araujo, Alessandro [Brazilian Agricultural Researc↗

AmeriFlux FLUXNET-1F BR-ITA MataFLUX: Multi-species tree restoration planting

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site BR-ITA MataFLUX: Multi-species tree restoration planting. This is the FLUXNET version of the carbon flux data for the site BR-ITA MataFLUX: Multi-species tree restoration planting produced by applying the standard ONEFlux (1F) software. Site Description - This tower is situated at the Itatinga Research Station (USP-ESALQ), located within the Brazilian Atlantic Forest. The station focuses on promoting forest research and features a landscape consisting of eucalyptus plantations and native species restoration areas.

Guillemot, Joannès [Cirad]↗

AmeriFlux FLUXNET-1F BR-SM1 Cachoeira do Sul Rice Paddy

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site BR-SM1 Cachoeira do Sul Rice Paddy. This is the FLUXNET version of the carbon flux data for the site BR-SM1 Cachoeira do Sul Rice Paddy produced by applying the standard ONEFlux (1F) software. Site Description - The site is a flooded rice paddy located in the Cachoeira do Sul, Rio Grande do Sul State, Brazil (latitude: -30.27°; longitude: -53.14°; altitude 40.5 m). The total cultivation area is approximately 1000 ha, subdivided into 100 mx100m plots. Flooded rice paddies have been used in this area since the 1980s and are a part of a wide lowland area susceptible to flooding by a stream (Pedro Paulo Stream). Channels and artificial reservoirs provide the water used.

Roberti, Debora Regina [Universidade Federal de Sa↗

AmeriFlux FLUXNET-1F BR-Ma2 Manaus - ZF2 K34

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site BR-Ma2 Manaus - ZF2 K34. This is the FLUXNET version of the carbon flux data for the site BR-Ma2 Manaus - ZF2 K34 produced by applying the standard ONEFlux (1F) software. Site Description - The K34 tower is deployed in a medium elevation plateau in the Cuieiras Biological Reserve, a primary forest area, property of INPA, 60Km north of Manaus, in the Km34 of the of the auxiliary road of the ZF2 Reserve.

Araujo, Alessandro [Embrapa Eastern Amazon]↗

AmeriFlux FLUXNET-1F BR-Xpw XomanoFlux

This is the AmeriFlux Management Project (AMP) created FLUXNET-1F version of the carbon flux data for the site BR-Xpw XomanoFlux. This is the FLUXNET version of the carbon flux data for the site BR-Xpw XomanoFlux produced by applying the standard ONEFlux (1F) software. Site Description - The site is located in the northern Pantanal, in central South America. The site is a grazing area used for cattle ranching and is subject to seasonal flooding during rainy seasons (November to April). Dry seasons are typically May to October.

Dalmagro, Higo [Universidade de Cuiabá - UNIC]↗

Volatile element chemistry in the solar nebula - Na, K, F, Cl, Br, and P

The results of the most extensive set to date of thermodynamic calculations on the equilibrium chemistry of several hundred compounds of the elements Na, K, F, Cl, Br, and P in a solar composition system are reported. Two extreme models of accretion are investigated. In one extreme complete chemical equilibrium between condensates and gases is maintained because the time scale for accretion is long compared to the time scale for cooling or dissipation of the nebula. Condensates formed in this homogeneous accretion model include several phases such as whitlockite, alkali feldspars, and apatite minerals which are found in chondrites. In the other extreme complete isolation of newly formed condensates from prior condensates and gases occurs due to a time scale for accretion that is short relative to the time required for nebular cooling or dissipation. The condensates produced in this heterogeneous accretion model include alkali sulfides, ammonium halides, and ammonium phosphates. None of these phases are found in chondrites. Available observations of the Na, K, F, Cl, Br, and P elemental abundances in the terrestrial planets are found to be compatible with the predictions of the homogeneous accretion model.

Fegley, B., Jr.↗

Rate constant for the reaction SO + BrO yields SO2 + Br

The rate of the radical-radical reaction SO + BrO yields SO2 + Br has been determined at 298 K in a discharge flow system near 1 torr pressure with detection of SO and BrO via collision-free sampling mass spectrometry. The rate constant was determined using two different methods: measuring the decay of SO radicals in the presence of an excess of BrO and measuring the decay of BrO radicals in excess SO. The results from the two methods are in reasonable agreement and the simple mean of the two values gives the recommended rate constant at 298 K, k = (5.7 + or - 2.0) x 10 to the -11th cu cm/s. This represents the first determination of this rate constant and it is consistent with a previously derived lower limit based on SO2 formation. Comparison is made with other radical-radical reactions involving SO or BrO. The reaction SO + BrO yields SO2 + Br is of interest for models of the upper atmosphere of the earth and provides a potential coupling between atmospheric sulfur and bromine chemistry.

Brunning, J.↗

High-resolution continuum and Br (gamma) imaging observations of M82

We report high angular resolution (about 0.6 sec), broad-band imaging at 1.2 microns (J band), 1.6 microns (H band), 2.2 microns (K band), and 3.7 microns (L' band) of the central 110 sec x 21 sec (1.65 kpc x 0.32 kpc) of the nearby starburst galaxy M82. We also present spectral imaging with 90 km/s resolution in the Br (gamma) (2.17 microns) hydrogen recombination line covering the central 16 sec x 16 sec (240 pc x 240 pc) of this edge-on, disk galaxy. The broad-band mosaics reveal two plateaus of emission indicative of an inner disk of stars and perhaps a larger bar structure. Color maps reveal an extinction ridge running along the central kiloparsec which is strongest at the nucleus and on the western side. The dust emission is more symmetric, suggesting that a dust lane is in front of the stellar population to the west of the nucleus, and behind the stars to the east; this is again suggestive of a stellar bar with leading dust lanes. Channel maps and a position-velocity image of the Br (gamma) reveal two lobes and are consistent with the interpretation that the ionized gas, and hence, the young massive stars are distributed in a toroid of H II regions surrounding the nucleus.

Larkin, J. E.↗

Kinetics of the Reactions of Cl((sup 2)P(sub J)) and Br((sup 2)P(sub 3/2)) with O3

A laser flash photolysis-resonance fluorescence technique has been employed to study the kinetics of the important stratospheric reactions Cl((sup 2)P(sub J)) + O3 yields ClO + O2 and Br((sup 2)P(sub 3/2)) + O3 yields BrO + O2 as a function of temperature. The temperature dependence observed for the Cl((sup 2)P(sub J)) + O3 reaction is nonArrhenius, but can be adequately described by the following two Arrhenius expressions (units are cu cm/(molecule.s), errors are 2 sigma and represent precision only): k(sub 1)(T) = (1.19 +/- 0.21) x 10(exp -11) exp[(-33 +/- 37)/T] for T = 189-269 K and k(sub 1)(T) = (2.49 +/- 0.38) x 10(exp -11) exp[(-233 +/- 46)/T] for 269-385 K. At temperatures below 230 K, the rate coefficients determined in this study are faster than any reported previously. Incorporation of our values for k(sub 1)(T) into stratospheric models would increase calculated ClO levels and decrease calculated HCI levels; hence the calculated efficiency of ClO catalyzed ozone destruction would increase. The temperature dependence observed for the Br((sup 2)P(sub 3/2)) + O3 reaction is adequately described by the following Arrhenius expression (units are cu cm/(molecule.s), errors are 2 sigma and represent precision only): k(sub 2)(T) = (1.50 +/- 0.16) x 10(exp -11)exp[(-775 +/- 30)/T for 195-392 K. While not in quantitative agreement with Arrhenius parameters reported in most previous studies, our results almost exactly reproduce the average of all earlier studies and therefore will not affect the choice of k(sub 2)(T) for use in modeling stratospheric BrO2 chemistry.

Nicovich, J. M.↗

The evaporation path of seawater and the coprecipitation of Br- and K+ with halite

Brines and salt were sampled at the Morton Bahamas solar salt production facility on Great Inagua Island in the Bahamas. The brines were analyzed by ion chromatography to define more precisely than heretofore the evaporation path of seawater to the end of the halite facies. At Inagua, calcium carbonate begins to precipitate at a brine concentration factor of 1.8 times that of seawater. Gypsum begins to precipitate at a brine concentration of 3.8 times seawater, and halite at a concentration factor of 10.6. Three of the most concentrated brines from Inagua (40 times seawater) were evaporated further in the laboratory. Magnesium sulfate first precipitated at brine concentrations about 70 times those of seawater, and potassium-bearing phases began to precipitate for these brines at concentrations greater than 90 times those of seawater. The distribution of coefficients of Br- and K+ between brines and halite were determined by combining analytical data for the Inagua brines with measurements of the Br- and K+ content of halites from Inagua and of halite which had precipitated from Inagua brines during storage. The observed average value of DBr- is 0.032, in good agreement with some of the previous measurements. The measured values of DK+ are highly variable (0.001 to 0.021); DK+ for halite precipitated early in the halite facies is in the vicinity of 0.015.

NASA Discipline Exobiology↗

Correlative analysis of CsPbBr2Hal (Hal = Cl, Br, I) meltcrystallization paramete

Abstract — Metal halide perovskites (MHPs) are an exciting research topic as they have the potential to make solar cells that are both more efficient than current siliconbased designs and have a wider range of applications. In this work the crystallization of CsPbBr2Hal (Hal = Cl, Br, I) halide perovskite melts were studied by the differential thermal analysis method. It was established that the crystallization of CsPbBr2Hal (Hal = Cl, Br, I) melts can be “hot” (i.e., at temperatures above the point of the alloy’s start-melting temperature) or with supercooling. The replacement of the bromine atom with another halogen atom leads to a shift of the dwell temperature range, at which “hot” crystallization takes place, from 830-846 K for CsPbBr3 to 807-832 K for CsPbBr2Cl and 741-768 K for CsPbBr2I. The activation energy of “hot” crystallization decreases in the same order. A linear dependence between the pre-exponential factor (ln(𝑽𝑽𝒄𝒄𝒄𝒄𝒄𝒄𝒔𝒔𝒕𝒕 𝟎𝟎 )) and the activation energy (Ea) of the crystallization process is revealed from the experimental data, proving the compensation effect.

Kopach, O.↗

Composition-Dependent Photoluminescence Properties and Anti-Counterfeiting Applications of A 2 AgX 3 (A = Rb, Cs; X = Cl, Br, I)

Copper(I) halides are emerging as attractive alternatives to lead halide perovskites for optical and electronic applications. However, blue-emitting all-inorganic copper(I) halides suffer from poor stability and lack of tunability of their photoluminescence (PL) properties. In this work, the preparation of silver(I) halides A 2 AgX 3 (A = Rb, Cs; X = Cl, Br, I) through solid-state synthesis is reported. In contrast to the Cu(I) analogs, A 2 AgX 3 are broad-band emitters sensitive to A and X site substitutions. First-principle calculations show that defect-bound excitons are responsible for the observed main PL peaks in Rb 2 AgX 3 and that self-trapped excitons (STEs) contribute to a minor PL peak in Rb 2 AgBr 3 . This is in sharp contrast to Rb 2 CuX 3 , in which the PL is dominated by the emission by STEs. Moreover, the replacement of Cu(I) with Ag(I) in A 2 AgX 3 significantly improves photostability and stability in the air under ambient conditions, which enables their consideration for practical applications. Thus, luminescent inks based on A 2 AgX 3 are prepared and successfully used in anti-counterfeiting applications. The excellent light emission properties, significantly improved stability, simple preparation method, and tunable light emission properties demonstrated by A 2 AgX 3 suggest that silver(I) halides may be attractive alternatives to toxic lead halide perovskites and unstable copper(I) halides for optical applications.

36 MATERIALS SCIENCE↗