2,450 research outputs found

    Stability relationship for water droplet crystallization with the NASA Lewis icing spray

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    In order to produce small droplets for icing cloud simulation, high pressure air atomizing nozzles are used. For certain icing testing applications, median drop sizes as small as 5 mm are needed, which require air atomizing pressures greater than 3000 kPa. Isentropic expansion of the ambient temperature atomizing air to atmospheric pressure can result in air stream temperatures of -160 C which results in ice crystals forming in the cloud. To avoid such low temperatures, it is necessary to heat the air and water to high initial temperatures. An icing spray research program was conducted to map the temperatures below which ice crystals form. A soot slide technique was used to determine the presence of crystals in the spray

    Calculation of kinetic rate constants from thermodynamic data

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    A new scheme for relating the absolute value for the kinetic rate constant k to the thermodynamic constant Kp is developed for gases. In this report the forward and reverse rate constants are individually related to the thermodynamic data. The kinetic rate constants computed from thermodynamics compare well with the current kinetic rate constants. This method is self consistent and does not have extensive rules. It is first demonstrated and calibrated by computing the HBr reaction from H2 and Br2. This method then is used on other reactions

    Simplified Two-Time Step Method for Calculating Combustion and Emission Rates of Jet-A and Methane Fuel With and Without Water Injection

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    A simplified kinetic scheme for Jet-A, and methane fuels with water injection was developed to be used in numerical combustion codes, such as the National Combustor Code (NCC) or even simple FORTRAN codes. The two time step method is either an initial time averaged value (step one) or an instantaneous value (step two). The switch is based on the water concentration in moles/cc of 1x10(exp -20). The results presented here results in a correlation that gives the chemical kinetic time as two separate functions. This two time step method is used as opposed to a one step time averaged method previously developed to determine the chemical kinetic time with increased accuracy. The first time averaged step is used at the initial times for smaller water concentrations. This gives the average chemical kinetic time as a function of initial overall fuel air ratio, initial water to fuel mass ratio, temperature, and pressure. The second instantaneous step, to be used with higher water concentrations, gives the chemical kinetic time as a function of instantaneous fuel and water mole concentration, pressure and temperature (T4). The simple correlations would then be compared to the turbulent mixing times to determine the limiting rates of the reaction. The NASA Glenn GLSENS kinetics code calculates the reaction rates and rate constants for each species in a kinetic scheme for finite kinetic rates. These reaction rates are used to calculate the necessary chemical kinetic times. Chemical kinetic time equations for fuel, carbon monoxide and NOx are obtained for Jet-A fuel and methane with and without water injection to water mass loadings of 2/1 water to fuel. A similar correlation was also developed using data from NASA's Chemical Equilibrium Applications (CEA) code to determine the equilibrium concentrations of carbon monoxide and nitrogen oxide as functions of overall equivalence ratio, water to fuel mass ratio, pressure and temperature (T3). The temperature of the gas entering the turbine (T4) was also correlated as a function of the initial combustor temperature (T3), equivalence ratio, water to fuel mass ratio, and pressure

    Anisotropic intrinsic lattice thermal conductivity of phosphorene from first principles

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    Phosphorene, the single layer counterpart of black phosphorus, is a novel two-dimensional semiconductor with high carrier mobility and a large fundamental direct band gap, which has attracted tremendous interest recently. Its potential applications in nano-electronics and thermoelectrics call for a fundamental study of the phonon transport. Here, we calculate the intrinsic lattice thermal conductivity of phosphorene by solving the phonon Boltzmann transport equation (BTE) based on first-principles calculations. The thermal conductivity of phosphorene at 300 K300\,\mathrm{K} is 30.15 Wm−1K−130.15\,\mathrm{Wm^{-1}K^{-1}} (zigzag) and 13.65 Wm−1K−113.65\,\mathrm{Wm^{-1}K^{-1}} (armchair), showing an obvious anisotropy along different directions. The calculated thermal conductivity fits perfectly to the inverse relation with temperature when the temperature is higher than Debye temperature (ΘD=278.66 K\Theta_D = 278.66\,\mathrm{K}). In comparison to graphene, the minor contribution around 5%5\% of the ZA mode is responsible for the low thermal conductivity of phosphorene. In addition, the representative mean free path (MFP), a critical size for phonon transport, is also obtained.Comment: 5 pages and 6 figures, Supplemental Material available as http://www.rsc.org/suppdata/cp/c4/c4cp04858j/c4cp04858j1.pd

    Arctic rock coast responses under a changing climate

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    It has been widely reported that Arctic sea ice has decreased in both extent and thickness, coupled with steadily rising mean annual temperatures. These trends have been particularly severe along the rock coast of southern Svalbard. Concerns have been raised over the potential for higher energy storms and longer ice-free open water seasons to increase the exposure of Arctic coasts, and consequently the concentration of infrastructure critical to Arctic community survival, to enhanced rates of erosion. Here we present and apply innovative remote sensing, monitoring and process analyses to assess the impact of recent coastal climatic changes. High resolution analyses demonstrate that the small scale (<0.001 m3) changes that are rarely considered quantitatively exhibit geomorphic responses distinct from those of larger, more readily detected cliff failures. We monitor temperature depth profiles in both the shore platform and the cliff face to show rock sensitivity over time to both global and local influences. The results demonstrate the efficacy of thermal processes on Arctic rock cliffs relative to platforms, and may hold implications for understanding strandflat development rates. New three-dimensional thermography (thermal mapping) and process zone characterisation has been used to spatially assess the sensitivity of Arctic rock coast responses to contemporary processes on deglaciating coasts. Through the spatial and temporal analyses of key geomorphic behaviour zones and comparison over a range of sites, the complex and changing interplay between subaerial weathering and cryogenic and intertidal processes has been highlighted. These data challenge long standing assumptions over the future of Arctic rock coasts and identify new, focused lines of enquiry on the decline in cryogenic processes and understanding the sensitivity of Arctic rock coasts to climatic changes
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