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Sample records for hastelloy n

  1. Hemispherical total emissivity of Hastelloy N with different surface conditions

    NASA Astrophysics Data System (ADS)

    Gordon, Andrew J.; Walton, Kyle L.; Ghosh, Tushar K.; Loyalka, Sudarshan K.; Viswanath, Dabir S.; Tompson, Robert V.

    2012-07-01

    The hemispherical total emissivity of Hastelloy N (a candidate structural material for Next Generation Nuclear Plants (NGNPs), particularly for the molten fluoride cooled reactors) was measured using an experimental set-up that was constructed in accordance with the standard ASTM C835-06. The material surface conditions included: (i) 'as received' (original) sample from the supplier; (ii) samples with increased surface roughness through sand blasting; (iii) oxidized surface, and (iv) samples coated with graphite powder. The emissivity of the as received samples varied from around 0.22 to 0.28 in the temperature range of 473 K to 1498 K. The emissivity increased when the roughness of the surface increased compared to an as received sample. When Hastelloy N was oxidized in air at 1153 K or coated with graphite powder, its emissivity increased substantially. The sample sand blasted with 60 grit beads and sprinkled with graphite powder showed an increase of emissivity from 0.2 to 0.60 at 473 K and from 0.25 to 0.67 at 1473 K. The oxidized surface showed a similar behavior: an increase in emissivity compared to an unoxidized sample. This increase in emissivity has strong favorable safety implications in terms of decay heat removal in post-accident environments. The data were compared with another Hastelloy family member, Hastelloy X.

  2. Long-term corrosion behaviors of Hastelloy-N and Hastelloy-B3 in moisture-containing molten FLiNaK salt environments

    NASA Astrophysics Data System (ADS)

    Ouyang, Fan-Yi; Chang, Chi-Hung; Kai, Ji-Jung

    2014-03-01

    This study investigated long-term corrosion behaviors of Ni-based Hastelloy-N and Hastelloy-B3 under moisture-containing molten alkali fluoride salt (LiF-NaF-KF: 46.5-11.5-42%) environment at an ambient temperature of 700 °C. The Hastelloy-N and Hastelloy-B3 experienced similar weight losses for tested duration of 100-1000 h, which was caused by aggregate dissolution of Cr and Mo into FLiNaK salts. The corrosion rate of both alloys was high initially, but then reduced during the course of the test. The alleviated corrosion rate was due to the depletion of Cr and Mo near surface of the alloys and thus the long-term corrosion rate was controlled by diffusion of Cr and Mo outward to the alloy surface. The results of microstructural characterization revealed that the corrosion pattern for both alloys tended to be intergranular corrosion at early stage of corrosion test, and then transferred to general corrosion for longer immersion hours.

  3. Machinability of hastelloy C-276 using Hot-pressed sintered Ti(C7N3)-based cermet cutting tools

    NASA Astrophysics Data System (ADS)

    Xu, Kaitao; Zou, Bin; Huang, Chuanzhen; Yao, Yang; Zhou, Huijun; Liu, Zhanqiang

    2015-05-01

    C-276 nickel-based alloy is a difficult-to-cut material. In high-speed machining of Hastelloy C-276, notching is a prominent failure mode due to high mechanical properties of work piece, which results in the short tool life and low productivity. In this paper, a newly developed Ti(C7N3)-based cermet insert manufactured by a hot-pressing method is used to machine the C-276 nickel-based alloy, and its cutting performances are studied. Based on orthogonal experiment method, the influence of cutting parameters on tool life, material removal rates and surface roughness are investigated. Experimental research results indicate that the optimal cutting condition is a cutting speed of 50 m/min, depth of cut of 0.4 mm and feed rate of 0.15 mm/r if the tool life and material removal rates are considered comprehensively. In this case, the tool life is 32 min and material removal rates are 3000 mm3/min, which is appropriate to the rough machining. If the tool life and surface roughness are considered, the better cutting condition is a cutting speed of 75 m/min, depth of cut of 0.6 mm and feed rate of 0.1 mm/r. In this case, the surface roughness is 0.59μm. Notch wear, flank wear, chipping at the tool nose, built-up edge(BUE) and micro-cracks are found when Ti(C7N3)-based cermet insert turned Hastelloy C-276. Oxidation, adhesive, abrasive and diffusion are the wear mechanisms, which can be investigated by the observations of scanning electron microscope and energy-dispersive spectroscopy. This research will help to guide studies on the evaluation of machining parameters to further advance the productivity of nickel based alloy Hastelloy C-276 machining.

  4. Computational Thermodynamic Modeling of Hot Corrosion of Alloys Haynes 242 and HastelloyTM N for Molten Salt Service in Advanced High Temperature Reactors

    SciTech Connect

    V. Glazoff, Michael; Charit, Indrajt; Sabharwall, Piyush

    2014-09-17

    An evaluation of thermodynamic aspects of hot corrosion of the superalloys Haynes 242 and HastelloyTM N in the eutectic mixtures of KF and ZrF4 is carried out for development of Advanced High Temperature Reactor (AHTR). This work models the behavior of several superalloys, potential candidates for the AHTR, using computational thermodynamics tool (ThermoCalc), leading to the development of thermodynamic description of the molten salt eutectic mixtures, and on that basis, mechanistic prediction of hot corrosion. The results from these studies indicated that the principal mechanism of hot corrosion was associated with chromium leaching for all of the superalloys described above. However, HastelloyTM N displayed the best hot corrosion performance. This was not surprising given it was developed originally to withstand the harsh conditions of molten salt environment. However, the results obtained in this study provided confidence in the employed methods of computational thermodynamics and could be further used for future alloy design efforts. Finally, several potential solutions to mitigate hot corrosion were proposed for further exploration, including coating development and controlled scaling of intermediate compounds in the KF-ZrF4 system.

  5. Crack propagation in Hastelloy X

    SciTech Connect

    Weerasooriya, T.; Strizak, J.P.

    1980-05-01

    The fatigue and creep crack growth rates of Hastelloy X were examined both in air and impure helium. Creep crack growth rate is higher in air and impure helium at 650/sup 0/C. Initial creep crack growth from the original sharp fatigue crack is by an intergranular mode of fracture. As the cracking accelerates at higher stress intensities, growth is by a mixed mode of both intergranular and transgranular fracture. Fatigue crack growth rate increases with increasing temperature and decreasing frequency for the range of stress intensities reported in the literature and is lower in impure helium than in air.

  6. Relation of Engine Turbine-blade Life to Stress-rupture Properties of the Alloys, Stellite 21, Hastelloy B, Cast S-816, Forged S-816, X-40, Nimonic 80, Refractaloy 26, N-155, and Inconel X

    NASA Technical Reports Server (NTRS)

    Garrett, F B; Yaker, C

    1951-01-01

    An investigation was conducted to relate the engine performance of the heat-resistant alloys, Stellite 21, Hastelloy B, cast S-816, forged S-816, X-40, Nimonic 80, Refractory 26, N-155, and Iconel X to their stress-rupture properties. The engine test consisted of the repetition of a 20-minute cycle, 15 minutes at rated speed and approximately 5 minutes at idle. The results of the investigation indicated a direct correlation between stress-rupture life and blade life for the relatively low-strength alloys. The stress-rupture life and blade life for the relatively high-strength alloys did not correlate because of the effects of the vibratory stresses and the corrosive-gas atmosphere.

  7. Effects of room-temperature tensile fatigue on critical current and n-value of IBAD-MOCVD YBa2Cu3O7-x /Hastelloy coated conductor

    NASA Astrophysics Data System (ADS)

    Rogers, Samuel; Kan Chan, Wan; Schwartz, Justin

    2016-08-01

    REBa2Cu3O7-x (REBCO) coated conductors potentially enable a multitude of superconducting applications, over a wide range of operating temperatures and magnetic fields, including high-field magnets, energy storage devices, motors, generators, and power transmission systems (Zhang et al 2013 IEEE Trans. Appl. Supercond. 23 5700704). Many of these are AC applications and thus the fatigue properties may be limiting (Vincent et al 2013 IEEE Trans. Appl. Supercond. 23 5700805). Previous electromechanical studies have determined the performance of REBCO conductors under single cycle loads (Barth et al 2015 Supercond. Sci. Technol. 28 045011), but an understanding of the fatigue properties is lacking. Here the fatigue behavior of commercial ion beam assisted deposition-metal organic chemical vapor deposition REBCO conductors on Hastelloy substrates is reported for axial tensile strains up to 0.5% and up to 100 000 cycles. Failure mechanisms are investigated via microstructural studies. Results show that REBCO conductors retained I c(ɛ)/I c0 = 0.9 for 10 000 cycles at ɛ = 0.35% and ɛ = 0.45% strain, and ɛ = 0.5% for 100 cycles. The main cause of fatigue degradation in REBCO conductors is crack propagation that initiates at the slitting defects that result from the manufacturing process.

  8. Air oxidation and seawater corrosion of Hastelloy S and Hastelloy C-4

    SciTech Connect

    Fullam, H.T.

    1980-03-01

    A program is currently under way at the Pacific Northwest Laboratory (PNL) to develop the data and technology needed to permit the licensing of /sup 90/SrF/sub 2/ as a radioisotope heat source fuel for terrestrial applications. The WESF /sup 90/SrF/sub 2/ storage capsule consists of a Hastelloy C-276 inner capsule (2 in. I.D. x 19 in. long) and a 316L stainless steel outer capsule (2-3/8 in. I.D. x 20 in. long). Preliminary experimental tests and theoretical calculations show that the WESF storage capsule is incapable of meeting current licensing requirements for heat sources that are to be used for terrestrial applications. Therefore, the DOE decision was to develop a new heat source design that would retain the existing WESF Hastelloy C-276 inner capsule and replace the current WESF outer capsule with a new outer capsule capable of meeting current licensing requirements. Based on a number of factors, Hastelloy S was selected as the outer capsule material. Hastelloy C-4 was selected as a backup material in case the Hastelloy S had to be rejected for any reason. This report summarizes the results of studies carried out to determine the effects of both air oxidation at heat source operating temperatures and seawater corrosion on the tensile properties of the outer capsule materials.

  9. Effects of oxidation on the impact energy of Hastelloy S and Hastelloy C-4 Charpy V-notch specimens heated in air at 600 to 800

    SciTech Connect

    Fullam, H.T.

    1981-01-01

    The /sup 90/SrF/sub 2/ heat source being developed at PNL utilizes a Hastelloy S or Hastelloy C-4 outer capsule having a 0.5-in.-thick wall to contain the Hastelloy C-276 inner capsule. The primary objective of the study was to demonstrate that the air oxidation of the outer capsule that could occur during heat-source service would not degrade the ductility and Charpy impact strength of the capsule below the licensing requirements given in Section 1.1. The /sup 90/SrF/sub 2/ heat source under development is intended for general-purpose use. Compatibility considerations limit the interface temperature between the /sup 90/SrF/sub 2/ and Hastelloy C-276 inner capsule to a maximum of 800/sup 0/C. The outer capsule surface temperature will be somewhat less than 800/sup 0/C, and depending on the service, may be substantially lower. The oxidation tests were therefore carried out at 600/sup 0/ to 800/sup 0/C for exposures up to 10,000h to cover the range of temperature the outer capsule might expect to encounter in service. The results showed that the oxidation of Hastelloy S and Hastelloy C-4 in air at 600/sup 0/ to 800/sup 0/C is very slow, and both alloys form adherent oxide layers that serve to protect the underlying metal. Subsurface attack of Hastelloy S and Hastelloy C-4 due to oxidation was greater than expected, considering the slow oxidation rates of the two alloys at 600/sup 0/ to 800/sup 0/C. Estimates of subsurface attack, determined from micrographs of the oxidized specimens, showed erratic results and it was impossible to assign any type of rate equation to the subsurface attack. A conservative estimate of long-term effects can be made using a linear extrapolation of the test results. There were no significant differences between the room-temperature Charpy impact energy of Hastelloy S and Hastelloy C-4 specimens oxidized in air at 600/sup 0/ to 800/sup 0/C and control specimens heated in vacuum.

  10. Influence of temperature, environment, and thermal aging on the continuous cycle fatigue behavior of Hastelloy X and Inconel 617

    SciTech Connect

    Strizak, J.P.; Brinkman, C.R.; Booker, M.K.; Rittenhouse, P.L.

    1982-04-01

    Results are presented for strain-controlled fatigue and tensile tests for two nickel-base, solution-hardened reference structural alloys for use in several High-Temperature Gas-Cooled Reactor (HTGR) concepts. These alloys, Hastelloy X and Inconel 617, were tested from room temperature to 871/sup 0/C in air and impure helium. Materials were tested in both the solution-annealed and the preaged conditios, in which aging consisted of isothermal exposure at one of several temperatures for periods of up to 20,000 h. Comparisons are given between the strain-controlled fatigue lives of these and several other commonly used alloys, all tested at 538/sup 0/C. An analysis is also presented of the continuous cycle fatigue data obtained from room temperature to 427/sup 0/C for Hastelloy G, Hastelloy X, Hastelloy C-276, and Hastelloy C-4, an effort undertaken in support of ASME code development.

  11. Effects of high temperature brazing and thermal cycling on mechanical properties of Hastelloy X.

    NASA Technical Reports Server (NTRS)

    Dicus, D. L.; Buckley, J. D.

    1973-01-01

    Data are presented on the effects of brazing alloy, brazing operation, thermal cycling, and combinations of these on the yield strength, elongation, ultimate tensile strength, and fatigue life of thin gage Hastelloy X. These data show that brazing with a Ni-Pd-Au alloy at 1461 K resulted in reductions of 35 percent in yield strength and elongation, 6 percent in ultimate tensile strength, and 18 percent in fatigue limit of Hastelloy X, as compared with as-received material. Subsequent exposure to 200 thermal cycles between 533 K and 1144 K after brazing caused further losses of 4 percent in yield strength, 8 percent in ultimate tensile strength, and 6 percent in fatigue limit.

  12. Creep-rupture tests of internally pressurized Hastelloy-X tubes

    NASA Technical Reports Server (NTRS)

    Gumto, K. H.; Colantino, G. J.

    1973-01-01

    Seamless Hastelloy-X tubes with 0.375-in. outside diameter and 0.025-in. wall thickness were tested to failure at temperatures from 1400 to 1650 F and internal helium pressures from 800 to 1800 psi. Lifetimes ranged from 58 to 3600 hr. The creep-rupture strength of the tubes was from 20 to 40 percent lower than that of sheet specimens. Larson-Miller correlations and photomicrographs of some specimens are presented.

  13. Permeation of hydrogen in hastelloy C-276 alloy at high temperature

    SciTech Connect

    Zhang, D.; Liu, W.; Qian, Y.; Que, J.

    2015-03-15

    Tritium is generated by the interaction of neutrons with the lithium and beryllium in the molten salt reactors (MSRs), which use FLiBe as one of solvents of fluoride fuel. Tritium as by-product in the MSRs is an important safety issue because it could easily diffuse into environment through high temperature heat exchangers. The experimental technique of gas driven permeation has been used to investigate the transport parameter of hydrogen in Hastelloy C-276 which is considered as one of the candidate for structure materials. The measurements were carried out at the temperature range of 400-800 Celsius degrees with hydrogen loading pressures ranging from 5*10{sup 3} to 4*10{sup 4} Pa. The H diffusive transport parameters for Hastelloy C-276 follow an Arrhenius law in this temperature range. Regarding diffusivity and Sieverts' constant, Hastelloy C-276 has lower values compared with Ni201 alloy. The possible reason may be the trapping effects, which were formed by the alloying elements of Mo and Cr in the matrix. At the same time, the thin oxidation layer formed by the high Cr content could lead to a slower dissociation process of H{sub 2} at the surface. (authors)

  14. Hardening mechanisms in a dynamic strain aging alloy, Hastelloy X, during isothermal and thermomechanical cyclic deformation

    NASA Technical Reports Server (NTRS)

    Miner, R. V.; Castelli, M. G.

    1992-01-01

    The relative contributions of the hardening mechanisms in Hastelloy X during cyclic deformation were investigated by conducting isothermal cyclic deformation tests within a total strain range of +/-0.3 pct and at several temperatures and strain rates, and thermomechanical tests within several different temperature limits. The results of the TEM examinations and special constant structure tests showed that the precipitation on dislocations of Cr23C6 contributed to hardening, but only after sufficient time above 500 C. Solute drag alone produced very considerable cyclic hardening. Heat dislocation densities, peaking around 10 exp 11 per sq cm, were found to develop at temperatures producing the greatest cyclic hardening.

  15. 2G HTS wires made on 30 μm thick Hastelloy substrate

    NASA Astrophysics Data System (ADS)

    Sundaram, A.; Zhang, Y.; Knoll, A. R.; Abraimov, D.; Brownsey, P.; Kasahara, M.; Carota, G. M.; Nakasaki, R.; Cameron, J. B.; Schwab, G.; Hope, L. V.; Schmidt, R. M.; Kuraseko, H.; Fukushima, T.; Hazelton, D. W.

    2016-10-01

    REBCO (RE = rare earth) based high temperature superconducting (HTS) wires are now being utilized for the development of electric and electromagnetic devices for various industrial, scientific and medical applications. In the last several years, the increasing efforts in using the so-called second generation (2G) HTS wires for some of the applications require a further increase in their engineering current density (J e). The applications are those typically related to high magnetic fields where the higher J e of a REBCO wire, in addition to its higher irreversibility fields and higher mechanical strength, is already a major advantage over other superconducting wires. An effective way to increase the J e is to decrease the total thickness of a wire, for which using a thinner substrate becomes an obvious and attractive approach. By using our IBAD-MOCVD (ion beam assisted deposition-metal organic chemical vapor deposition) technology we have successfully made 2G HTS wires using a Hastelloy® C276 substrate that is only 30 μm in thickness. By using this thinner substrate instead of the typical 50 μm thick substrate and with a same critical current (I c), the J e of a wire can be increased by 30% to 45% depending on the copper stabilizer thickness. In this paper, we report the fabrication and characterization of the 2G HTS wires made on the 30 μm thick Hastelloy® C276 substrate. It was shown that with the optimization in the processing protocol, the surface of the thinner Hastelloy® C276 substrate can be readily electropolished to the quality needed for the deposition of the buffer stack. Same in the architecture as that on the standard 50 μm thick substrate, the buffer stack made on the 30 μm thick substrate showed an in-plane texture with a Δϕ of around 6.7° in the LaMnO3 cap layer. Low-temperature in-field transport measurement results suggest that the wires on the thinner substrate had achieved equivalent superconducting performance, most importantly the I

  16. Thermomechanical deformation behavior of a dynamic strain aging alloy, Hastelloy X

    NASA Technical Reports Server (NTRS)

    Castelli, Michael G.; Miner, Robert V.; Robinson, David N.

    1992-01-01

    An experimental study was performed to identify the effects of dynamic strain aging (solute drag) and metallurgical instabilities under thermomechanical loading conditions. The study involved a series of closely controlled thermomechanical deformation tests on the solid-solution-strenghened nickel-base superalloy, Hastelloy X. This alloy exhibits a strong isothermal strain aging peak at approximately 600 C, promoted by the effects of solute drag and precipitation hardening. Macroscopic thermomechanical hardening trends are correlated with microstructural characteristics through the use of transmission electron microscopy. These observations are compared and contrasted with isothermal conditions. Thermomechanical behavior unique to the isothermal database is identified and discussed. The microstructural characteristics were shown to be dominated by effects associated with the highest temperature of the thermomechanical cycle. Results indicate that the deformation behavior of Hastelloy X is thermomechanically path dependent. In addition, guidance is given pertaining to deformation modeling in the context of macroscopic unified theory. An internal state variable is formulated to qualitatively reflect the isotropic hardening trends identified in the TMD experiments.

  17. Thermomechanical cyclic hardening behavior of Hastelloy-X. M.S. Thesis

    NASA Technical Reports Server (NTRS)

    Bartolotta, P. A.

    1985-01-01

    Experimental evidence of thermomechanical history dependence on the cyclic hardening behavior of a representative combustor liner material Hastelloy-X is presented, along with a discussion about the relevant concept of thermomechanical path dependence. Based on the experimental results, a discussion is given on the inadequacy of formulating nonisothermal constitutive equations solely on the basis of isothermal testing. Finally, the essence of a mathematical representation of thermoviscoplasticity is presented that qualitatively accounts for the observed hereditary behavior. This is achieved by formulating the scaler evolutionary equation in an established viscoplastic theory to reflect thermomechanical path dependence. Although the necessary nonisothermal tests for further quantifying the thermoviscoplastic model have been identified, such data are not yet available.

  18. The effects of high-temperature brazing and thermal cycling on the mechanical properties of Hastelloy X

    NASA Technical Reports Server (NTRS)

    Dicus, D. L.; Buckley, J. D.

    1972-01-01

    Data are presented on the effects of brazing alloy, brazing operation, thermal cycling, and combinations of these on the yield strength, elongation, tensile strength, and fatigue life of thin gage Hastelloy X. These data show that brazing at 1461 K (2170 F) with a Ni-Pd-Au alloy and subsequent exposure to 200 service thermal cycles between 533 and 1144 K (500 and 1600 F) result in reduction of as much as 39 percent in yield strength, 33 percent in elongation, 14 percent in tensile strength, and 26 percent in fatigue limit of Hastelloy X, as compared to as-received materials. These property losses are primarily caused by the brazing operation rather than the subsequent service thermal cycles.

  19. Material Data Representation of Hysteresis Loops for Hastelloy X Using Artificial Neural Networks

    NASA Technical Reports Server (NTRS)

    Alam, Javed; Berke, Laszlo; Murthy, Pappu L. N.

    1993-01-01

    The artificial neural network (ANN) model proposed by Rumelhart, Hinton, and Williams is applied to develop a functional approximation of material data in the form of hysteresis loops from a nickel-base superalloy, Hastelloy X. Several different ANN configurations are used to model hysteresis loops at different cycles for this alloy. The ANN models were successful in reproducing the hysteresis loops used for its training. However, because of sharp bends at the two ends of hysteresis loops, a drift occurs at the corners of the loops where loading changes to unloading and vice versa (the sharp bends occurred when the stress-strain curves were reproduced by adding stress increments to the preceding values of the stresses). Therefore, it is possible only to reproduce half of the loading path. The generalization capability of the network was tested by using additional data for two other hysteresis loops at different cycles. The results were in good agreement. Also, the use of ANN led to a data compression ratio of approximately 22:1.

  20. Laser texturing of Hastelloy C276 alloy surface for improved hydrophobicity and friction coefficient

    NASA Astrophysics Data System (ADS)

    Yilbas, B. S.; Ali, H.

    2016-03-01

    Laser treatment of Hastelloy C276 alloy is carried out under the high pressure nitrogen assisting gas environment. Morphological and metallurgical changes in the laser treated layer are examined using the analytical tools including, scanning electron and atomic force microscopes, X-ray diffraction, energy dispersive spectroscopy, and Fourier transform infrared spectroscopy. Microhardness is measured and the residual stress formed in the laser treated surface is determined from the X-ray data. The hydrophibicity of the laser treated surface is assessed using the sessile drop method. Friction coefficient of the laser treated layer is obtained incorporating the micro-tribometer. It is found that closely spaced laser canning tracks create a self-annealing effect in the laser treated layer and lowers the thermal stress levels through modifying the cooling rates at the surface. A dense structure, consisting of fine size grains, enhances the microhardness of the surface. The residual stress formed at the surface is compressive and it is in the order of -800 MPa. Laser treatment improves the surface hydrophobicity significantly because of the formation of surface texture composing of micro/nano-pillars.

  1. Compatibility of aluminide-coated Hastelloy x and Inconel 617 in a simulated gas-cooled reactor environment

    SciTech Connect

    Chin, J.; Johnson, W. R.; Chen, K.

    1982-03-01

    Commercially prepared aluminide coatings on Hastelloy X and Inconel 617 substrates were exposed to controlled-impurity helium at 850/sup 0/ and 950/sup 0/C for 3000 h. Optical and scanning electron (SEM) microscopy, electron microprobe profiles, and SEM X-ray mapping were used to evaluate and compare exposed and unexposed control samples. Four coatings were evaluated: aluminide, aluminide with platinum, aluminide with chromium, and aluminide with rhodium. With extended time at elevated temperature, nickel diffused into the aluminide coatings to form epsilon-phase (Ni/sub 3/Al). This diffusion was the primary cause of porosity formation at the aluminide/alloy interface.

  2. Collect Available Creep-Fatigue Data and Study Existing Creep-Fatigue Evaluation Procedures for Grade 91 and Hastelloy XR

    SciTech Connect

    Tai Asayama; Yukio Tachibana

    2007-09-30

    This report describes the results of investigation on Task 5 of DOE/ASME Materials Project based on a contract between ASME Standards Technology, LLC (ASME ST-LLC) and Japan Atomic Energy Agency (JAEA). Task 5 is to collect available creep-fatigue data and study existing creep-fatigue evaluation procedures for Grade 91 steel and Hastelloy XR. Part I of this report is devoted to Grade 91 steel. Existing creep-fatigue data were collected (Appendix A) and analyzed from the viewpoints of establishing a creep-fatigue procedure for VHTR design. A fair amount of creep-fatigue data has been obtained and creep-fatigue phenomena have been clarified to develop design standards mainly for fast breeder reactors. Following this, existing creep-fatigue procedures were studied and it was clarified that the creep-fatigue evaluation procedure of the ASME-NH has a lot of conservatisms and they were analyzed in detail from the viewpoints of the evaluation of creep damage of material. Based on the above studies, suggestions to improve the ASME-NH procedure along with necessary research and development items were presented. Part II of this report is devoted to Hastelloy XR. Existing creep-fatigue data used for development of the high temperature structural design guideline for High Temperature Gas-cooled Reactor (HTGR) were collected. Creep-fatigue evaluation procedure in the design guideline and its application to design of the intermediate heat exchanger (IHX) for High Temperature Engineering Test Reactor (HTTR) was described. Finally, some necessary research and development items in relation to creep-fatigue evaluation for Gen IV and VHTR reactors were presented.

  3. Low-cycle fatigue of Type 347 stainless steel and Hastelloy alloy X in hydrogen gas and in air at elevated temperatures

    NASA Technical Reports Server (NTRS)

    Jaske, C. E.; Rice, R. C.; Buchheit, R. D.; Roach, D. B.; Porfilio, T. L.

    1976-01-01

    An investigation was conducted to assess the low-cycle fatigue resistance of two alloys, Type 347 stainless steel and Hastelloy Alloy X, that were under consideration for use in nuclear-powered rocket vehicles. Constant-amplitude, strain-controlled fatigue tests were conducted under compressive strain cycling at a constant strain rate of 0.001/sec and at total axial strain ranges of 1.5, 3.0, and 5.0 %, in both laboratory-air and low-pressure hydrogen-gas environments at temperatures from 538 to 871 C. Specimens were obtained from three heats of Type 347 stainless steel bar and two heats of Hastelloy Alloy X. The tensile properties of each heat were determined at 21, 538, 649, and 760 C. The continuous cycling fatigue resistance was determined for each heat at temperatures of 538, 760, and 871 C. The Type 347 stainless steel exhibited equal or superior fatigue resistance to the Hastelloy Alloy X at all conditions of this study.

  4. Chemistry of glass-ceramic to metal bonding for header applications. I. Effect of treatments on Inconel 718 and Hastelloy C-276 metallic surfaces

    SciTech Connect

    Kramer, D P; Craven, S M; Schneider, R E; Moddeman, W E; Brohard, D W

    1984-02-02

    Auger electron spectroscopy and depth Auger profiling were used to study the surfaces of Inconel 718 and Hastelloy C-276. The metal surfaces were processed in the same manner as is presently being used in the manufacturing of glass-ceramic headers. At each step in the process, samples were studied with Auger spectroscopy to determine their resultant elemental surface composition and film thickness. In addition, the effect of a final plasma cleaning operation on the metal surface was examined. The results show that the type and concentration of surface species and the thickness of the surface oxides are dependent on the processing technique.

  5. High-temperature low-cycle fatigue and tensile properties of Hastelloy X and alloy 617 in air and HTGR-helium

    SciTech Connect

    Strizak, J.P.; Brinkman, C.R.; Rittenhouse, P.L.

    1981-01-01

    Results of strain controlled fatigue and tensile tests are presented for two nickel base solution hardened alloys which are reference structural alloys for use in several high temperature gas cooled reactor concepts. These alloys, Hastelloy X Inconel 617, were tested at temperatures ranging from room temperature to 871/sup 0/C in air and impure helium. Materials were tested in the solution annealed as well as in the pre-aged condition where aging consisted of isothermal exposure at one of several temperatures for periods of up to 20,000 h. Comparisons are also given between the strain controlled fatigue lives of these alloys and several other commonly used alloys all tested at 538/sup 0/C.

  6. Dielectric spectroscopy of Pb0.92La0.08Zr0.52Ti0.48O3 films on hastelloy substrates with and without LaNiO3 buffer layers

    NASA Astrophysics Data System (ADS)

    Narayanan, Manoj; Ma, Beihai; Balachandran, U. (Balu); Li, Wei

    2010-01-01

    Pb0.92La0.08Zr0.52Ti0.48O3 (PLZT) films were deposited by sol-gel synthesis on Hastelloy substrates with and without a LaNiO3 buffer. The dielectric properties were measured as a function of temperature and frequency to study the cause of dielectric degradation in PLZT films directly on hastelloy substrates. These measurements indicated an increased charge carrier activity in films without a buffer layer. We propose that a region of the film closer to the substrate surface is more oxygen deficient than the bulk and is responsible for the degradation in properties rather than the presence of a low parasitic secondary-phase interfacial layer such as NiOx.

  7. Spray pyrolysis of MgO templates on Hastelloy C276 and 310-austenitic stainless steel substrates for Y Ba2Cu3O7 (YBCO) deposition by pulsed laser deposition

    NASA Astrophysics Data System (ADS)

    Khateeb, Shadi Al; Button, T. W.; Abell, J. S.

    2010-09-01

    MgO thin films were deposited on Hastelloy C276 (HC) and 310 austenitic stainless steel by the spray pyrolysis technique, using magnesium nitrate and magnesium acetate as precursors. Thermogravimetrical analysis of the decomposition of the precursors was used to provide a guideline temperature for the thin film deposition. It was suggested that an amorphous MgO thin film was deposited on both 310-stainless steel and Hastelloy C-276 when using low concentration of the magnesium nitrate precursor. Higher concentrations were needed to obtain (200) oriented MgO films on C276. However, 310-stainless steel was found to not be a suitable substrate for MgO thin film deposition due to surface instability. A (200) oriented MgO thin film was grown on Hastelloy C276 using a magnesium acetate precursor at a much lower concentration compared to the nitrate precursor. The characterization of the thin films was done using scanning electron microscopy, x-ray photoelectron spectroscopy, atomic force microscopy, x-ray diffraction 2θ-scans, rocking curves (ω-scans), and pole figure measurements. MgO was found to have a very weak in-plane texture.

  8. Effect of Continuous and Pulsed Current Gas Tungsten Arc Welding on Dissimilar Weldments Between Hastelloy C-276/AISI 321 Austenitic Stainless Steel

    NASA Astrophysics Data System (ADS)

    Sharma, Sumitra; Taiwade, Ravindra V.; Vashishtha, Himanshu

    2017-03-01

    In the present investigation, an attempt has been made to join Hastelloy C-276 nickel-based superalloy and AISI 321 austenitic stainless steel using ERNiCrMo-4 filler. The joints were fabricated by continuous and pulsed current gas tungsten arc welding processes. Experimental studies to ascertain the structure-property co-relationship with or without pulsed current mode were carried out using an optical microscope and scanning electron microscope. Further, the energy-dispersive spectroscope was used to evaluate the extent of microsegregation. The microstructure of fusion zone was obtained as finer cellular dendritic structure for pulsed current mode, whereas columnar structure was formed with small amount of cellular structure for continuous current mode. The scanning electron microscope examination witnessed the existence of migrated grain boundaries at the weld interfaces. Moreover, the presence of secondary phases such as P and μ was observed in continuous current weld joints, whereas they were absent in pulsed current weld joints, which needs to be further characterized. Moreover, pulsed current joints resulted in narrower weld bead, refined morphology, reduced elemental segregation and improved strength of the welded joints. The outcomes of the present investigation would help in obtaining good quality dissimilar joints for industrial applications and AISI 321 ASS being cheaper consequently led to cost-effective design also.

  9. Effect of Continuous and Pulsed Current Gas Tungsten Arc Welding on Dissimilar Weldments Between Hastelloy C-276/AISI 321 Austenitic Stainless Steel

    NASA Astrophysics Data System (ADS)

    Sharma, Sumitra; Taiwade, Ravindra V.; Vashishtha, Himanshu

    2017-02-01

    In the present investigation, an attempt has been made to join Hastelloy C-276 nickel-based superalloy and AISI 321 austenitic stainless steel using ERNiCrMo-4 filler. The joints were fabricated by continuous and pulsed current gas tungsten arc welding processes. Experimental studies to ascertain the structure-property co-relationship with or without pulsed current mode were carried out using an optical microscope and scanning electron microscope. Further, the energy-dispersive spectroscope was used to evaluate the extent of microsegregation. The microstructure of fusion zone was obtained as finer cellular dendritic structure for pulsed current mode, whereas columnar structure was formed with small amount of cellular structure for continuous current mode. The scanning electron microscope examination witnessed the existence of migrated grain boundaries at the weld interfaces. Moreover, the presence of secondary phases such as P and μ was observed in continuous current weld joints, whereas they were absent in pulsed current weld joints, which needs to be further characterized. Moreover, pulsed current joints resulted in narrower weld bead, refined morphology, reduced elemental segregation and improved strength of the welded joints. The outcomes of the present investigation would help in obtaining good quality dissimilar joints for industrial applications and AISI 321 ASS being cheaper consequently led to cost-effective design also.

  10. Thermodynamic Assessment of Hot Corrosion Mechanisms of Superalloys Hastelloy N and Haynes 242 in Eutectic Mixture of Molten Salts KF and ZrF4

    SciTech Connect

    Michael V. Glazoff

    2012-02-01

    The KF - ZrF4 system was considered for the application as a heat exchange agent in molten salt nuclear reactors (MSRs) beginning with the work carried out at ORNL in early fifties. Based on a combination of excellent properties such as thermal conductivity, viscosity in the molten state, and other thermo-physical and rheological properties, it was selected as one of possible candidates for the nuclear reactor secondary heat exchanger loop.

  11. Atlas of Formability: Hastelloy C-22

    DTIC Science & Technology

    1992-09-30

    but the twin boundaries show the 8 presence of necklacing. 6 950(1742) 0.50 9 7 950(1742) 1.0 Elongated grains with -10 % of small 10 recrystallized...grains. Some necklacing at the twin boundaries and slip bands are present. 8 950(1742) 5.0 11 9 950(1742) 20.0 Elongated grains with -15 % of small...12 r.zcrystallized grains (-9 gm). Some necklacing around the elongated grains and twin boundaries . Slip bands are also present. 10 1000(1832) 0.001

  12. High-temperature corrosion of UNS N10003 in molten Li2BeF4 (FLiBe) salt

    DOE PAGES

    Zheng, Guiqiu; Kelleher, Brian; He, Lingfeng; ...

    2015-07-30

    Here, corrosion testing of Hastelloy N in molten fluoride salt was performed in purified molten 27LiF-BeF2 (66-34mol%) (FLiBe) salt at 700°C for 1000 hours, in pure nickel and graphite capsules. In the nickel capsule tests, the near-surface region of the alloy exhibited an about 200 nm porous structure, an approximately 3.5 μm chromium depleted region, and MoSi2 precipitates. In tests performed in graphite capsules, the alloy samples gained weight due to the formation of a variety of Cr3C2, Cr7C3, Mo2C and Cr23C6, carbide phases on the surface and in the subsurface regions of the alloy. A Cr depleted region wasmore » observed in the near-surface region where Mo thermally diffused toward either surface or grain boundary, which induced approximately 1.4 μm Ni3Fe alloy layer in this region. The carbide containing layer extended to about 7 μm underneath the Ni3Fe layer. The presence of graphite dramatically changes the mechanisms of corrosion attack in Hastelloy N in molten FLiBe salt. Evaluated by in terms of the depth of attack, graphite clearly accelerates corrosion, but the results appear to indicate that the formation of Cr23C6 phase might stabilize the Cr and mitigate its dissolution in molten FLiBe salt.« less

  13. Thermomechanical characterization of Hastelloy-X under uniaxial cyclic loading

    NASA Technical Reports Server (NTRS)

    Ellis, J. R.; Bartolotta, P. A.; Allen, G. P.; Robinson, D. N.

    1986-01-01

    In most high-temperature engineering applications, components are subjected to complex combinations of thermal and mechanical loading during service. A number of viscoplastic constitutive models were proposed which potentially can provide mathematical descriptions of material response under such conditions. Implementation of these models into large finite element codes such as MARC has already resulted in much improved inelastic analysis capability for hot-section aircraft engine components. However, a number of questions remain regarding the validity of methods adopted in characterizing these constitutive models for particular high-temperature materials. One area of concern is that the majority of experimental data available for this purpose are determined under isothermal conditions. This is in contrast to service conditions which, as noted above, almost always involve some form of thermal cycling. The obvious question arises as to whether a constitutive model characterized using an isothermal data base can adequately predict material response under thermomechanical conditions. An experimental program was initiated within the HOST program to address this particular concern. The results of the most recent isothermal and thermomechanical experiments are described.

  14. High-temperature corrosion of UNS N10003 in molten Li2BeF4 (FLiBe) salt

    SciTech Connect

    Zheng, Guiqiu; Kelleher, Brian; He, Lingfeng; Cao, Guoping; Anderson, Mark; Allen, Todd; Sridharan, Kumar

    2015-07-30

    Here, corrosion testing of Hastelloy N in molten fluoride salt was performed in purified molten 27LiF-BeF2 (66-34mol%) (FLiBe) salt at 700°C for 1000 hours, in pure nickel and graphite capsules. In the nickel capsule tests, the near-surface region of the alloy exhibited an about 200 nm porous structure, an approximately 3.5 μm chromium depleted region, and MoSi2 precipitates. In tests performed in graphite capsules, the alloy samples gained weight due to the formation of a variety of Cr3C2, Cr7C3, Mo2C and Cr23C6, carbide phases on the surface and in the subsurface regions of the alloy. A Cr depleted region was observed in the near-surface region where Mo thermally diffused toward either surface or grain boundary, which induced approximately 1.4 μm Ni3Fe alloy layer in this region. The carbide containing layer extended to about 7 μm underneath the Ni3Fe layer. The presence of graphite dramatically changes the mechanisms of corrosion attack in Hastelloy N in molten FLiBe salt. Evaluated by in terms of the depth of attack, graphite clearly accelerates corrosion, but the results appear to indicate that the formation of Cr23C6 phase might stabilize the Cr and mitigate its dissolution in molten FLiBe salt.

  15. Microscopic study of the structure of the Steel Ni-based Alloy: Hastelloy G35 Alloy

    NASA Astrophysics Data System (ADS)

    Sabir, F.; Ben Lenda, O.; Saissi, S.; Marbouh, K.; Tyouke, B.; Zerrouk, L.; Ibnlfassi, A.; Ouzaouit, K.; Elmadani, S.

    2017-03-01

    The study of the influence of heat treatment on changes of mechanical and structural properties of Steel Ni-based Alloy is a highly interdisciplinary topic at the interface of the physical chemistry of metallic materials, which also helps in environmental and economic protection.After heat treatment, the structural and micro-structural studies for the different transformation temperature led to identify phases formed and the morphology. This work has been carried out using different techniques: X-ray diffraction, optical microscopy and scanning electron microscopy.

  16. Evaluation of a sodium/Hastelloy-X heat pipe for wing leading edge cooling

    SciTech Connect

    Merrigan, M.A.; Sena, J.T.; Glass, D.E.

    1996-12-31

    This report covers assembly of a sodium heat pipe, testing to verify performance during start-up and under steady-state conditions with stagnation point heat loads to about 80 W/cm{sup 2}, performance analysis and evaluation. Evaluation of this leading edge cooling concept is offered and recommendations for further research discussed.

  17. Evaluation of Three Constitutive Models for the Prediction of Hastelloy X Elevated Temperature Cyclic Response

    NASA Technical Reports Server (NTRS)

    Moreno, V.

    1983-01-01

    The approach for the method development assumes that, for a thermally loaded structure, the overall strain history is defined by linear elastic analysis. The local stress history at a fatigue critical location is then determined from a one dimensional material behavior model and the local strain and temperature conditions. Three material models are currently being evaluated to assess their ability to predict relevant high temperature cyclic material response characteristics. They are: a time independent classical plasticity and creep representation, a time dependent viscoplastic model capable of predicting combined creep and plasticity effects, and an approximate elastic analysis approach that uses a series of stress-strain curves and a cyclic hardening model to determine reverse plasticity.

  18. Development of a Mathematical Model of Crevice Corrosion Propagation on Nickel Base Alloys in Natural and Chlorinated Sea Water

    DTIC Science & Technology

    1994-08-30

    then bromamines and chloramines are formed and the processes become even more complicated. [10]. 0 From the point of view of crevice corrosion ... Corrosion Propagation on Nickel Base Alloys in Natural and Chlorinated Sea Water Thi! os 7 -= n %:ý 7e~~r: :-ppcved tor piU&* : e --I . " dcktr!u-,J...Summary Crevice corrosion initiation and propagation of nickel base alloys Inconel 625, Hastelloy C276 and Hastelloy 22 in sea water and chlorinated sea

  19. N,N-Dimethylformamide

    Integrated Risk Information System (IRIS)

    N , N - Dimethylformamide ; CASRN 68 - 12 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarci

  20. N-N-Dimethylaniline

    Integrated Risk Information System (IRIS)

    N - N - Dimethylaniline ; CASRN 121 - 69 - 7 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcin

  1. Preliminary lifetime predictions for 304 stainless steel as the LANL ABC blanket material

    SciTech Connect

    Park, J.J.; Buksa, J.J.; Houts, M.G.; Arthur, E.D.

    1997-11-01

    The prediction of materials lifetime in the preconceptual Los Alamos National Laboratory (LANL) Accelerator-Based Conversion of Plutonium (ABC) is of utmost interest. Because Hastelloy N showed good corrosion resistance to the Oak Ridge National Laboratory Molten Salt Reactor Experiment fuel salt that is similar to the LANL ABC fuel salt, Hastelloy N was originally proposed for the LANL ABC blanket material. In this paper, the possibility of using 304 stainless steel as a replacement for the Hastelloy N is investigated in terms of corrosion issues and fluence-limit considerations. An attempt is made, based on the previous Fast Flux Test Facility design data, to predict the preliminary lifetime estimate of the 304 stainless steel used in the blanket region of the LANL ABC.

  2. N-Nitrosodi-N-propylamine

    Integrated Risk Information System (IRIS)

    N - Nitrosodi - N - propylamine ; CASRN 621 - 64 - 7 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for N

  3. 1/N

    SciTech Connect

    Coleman, S.

    1980-03-01

    There exist families of field theories with symmetry group SO(N) (or SU(N)) that become simpler as N becomes larger. More precisely, the solutions to these theories possess an expansion in powers of 1/N. This expansion is the subject of these lectures. The 1/N expansion can be used to analyze model field theories. The 1/N expansion is developed for phi/sup 4/ theory and applied to two two-dimensional models with similar combinatoric structures, the Gross-Neveu model and the CP/sup N-1/ model. These models display (in the leading 1/N approximation) such interesting phenomena as asymptotic freedom, dynamical symmetry breaking, dimensional transmutation, and non-perturbative confinement. It is possible that the 1/N expansion, with N the number of colors, might fruitfully be applied to quantum chromodynamics. Unfortunately, it is not possible to make a decisive test of the approximation, because no one knows how to compute even the first term in the expansion in closed form. However, it is possible to argue that this first term, whatever its detailed form, has many properties that are also shared by the real world, and which are otherwise underived from field theory. These include the saturation of scattering amplitudes by an infinite number of narrow resonances, the essential feature of dual-resonance models. (RWR)

  4. N-Nitroso-N-methylethylamine

    Integrated Risk Information System (IRIS)

    N - Nitroso - N - methylethylamine ; CASRN 10595 - 95 - 6 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments

  5. Large N

    NASA Astrophysics Data System (ADS)

    't Hooft, Gerard

    2002-09-01

    In the first part of this lecture, the 1/N expansion technique is illustrated for the case of the large-N sigma model. In large-N gauge theories, the 1/N expansion is tantamount to sorting the Feynman diagrams according to their degree of planarity, that is, the minimal genus of the plane onto which the diagram can be mapped without any crossings. This holds both for the usual perturbative expansion with respect to powers of ˜ {g}2 = g2N, as well as for the expansion of lattice theories in positive powers of 1/˜ {g}2. If there were no renormalization effects, the ˜ {g} expansion would have a finite radius of convergence. The zero-dimensional theory can be used for counting planar diagrams. It can be solved explicitly, so that the generating function for the number of diagrams with given 3-vertices and 4-vertices, can be derived exactly. This can be done for various kinds of Feynman diagrams. We end with some remarks about planar renormalization.

  6. .. P .,n

    NASA Website

    t~~ j~te~r~l aoc~~d b~f~r~ lift-off. ~~~~. zero for tni~ mi••ion ~~ 13~,16:~9;OOGmt. Te.i, r~,0rt has b~"n f~era.ea ~$oppl~ment11 to ... h ": r.. ...

  7. Study of metal corrosion using ac impedance techniques in the STS launch environment

    NASA Technical Reports Server (NTRS)

    Calle, Luz M.

    1989-01-01

    AC impedance measurements were performed to investigate the corrosion resistance of 19 alloys under conditions similar to the STS launch environment. The alloys were: Zirconium 702, Hastelloy C-22, Inconel 625, Hastelloy C-276, Hastelloy C-4, Inconel 600, 7Mo + N, Ferralium 255, Inco Alloy G-3, 20Cb-3, SS 904L, Inconel 825, SS 304LN, SS 316L, SS 317L, ES 2205, SS 304L, Hastelloy B-2, and Monel 400. AC impedance data were gathered for each alloy after one hour immersion time in each of the following three electrolyte solutions: 3.55 percent NaCl, 3.55 percent NaCl-0.1N HCl, and 3.55 percent NaCl-1.0N HCl. The data were analyzed qualitatively using the Nyquist plot and quantitatively using the Bode plot. Polarization resistance, Rp, values were obtained using the Bode plot. Zirconium 702 was the most corrosion resistant alloy in the three electrolytes. The ordering of the other alloys according the their resistance to corrosion varied as the concentration of hydrochloric acid in the electrolyte increased. The corrosion resistance of Zirconium 702 and Ferralium 255 increased as the concentration of hydrochloric acid in the electrolyte increased. The corrosion resistance of the other 17 alloys decreased as the concentration of the hyrdochloric acid in the electrolyte increased.

  8. Phenomenology of n - n ¯ oscillations revisited

    DOE PAGES

    Gardner, S.; Jafari, E.

    2015-05-22

    We revisit the phenomenology of n-n¯ oscillations in the presence of external magnetic fields, highlighting the role of spin. We show, contrary to long-held belief, that the n-n¯ transition rate need not be suppressed, opening new opportunities for its empirical study.

  9. Experimental verification of the Neuber relation at room and elevated temperatures. M.S. Thesis; [to predict stress-strain behavior in notched specimens of hastelloy x

    NASA Technical Reports Server (NTRS)

    Lucas, L. J.

    1982-01-01

    The accuracy of the Neuber equation at room temperature and 1,200 F as experimentally determined under cyclic load conditions with hold times. All strains were measured with an interferometric technique at both the local and remote regions of notched specimens. At room temperature, strains were obtained for the initial response at one load level and for cyclically stable conditions at four load levels. Stresses in notched members were simulated by subjecting smooth specimens to he same strains as were recorded on the notched specimen. Local stress-strain response was then predicted with excellent accuracy by subjecting a smooth specimen to limits established by the Neuber equation. Data at 1,200 F were obtained with the same experimental techniques but only in the cyclically stable conditions. The Neuber prediction at this temperature gave relatively accurate results in terms of predicting stress and strain points.

  10. Synthesis of terephthalonitrile N,N-dioxide

    NASA Technical Reports Server (NTRS)

    Vanburen, K. E.

    1973-01-01

    The preparation is described of terephthalonitrile N,N prime-dioxide by the chlorination of terephthalaldehyde dioxime to yield terephthalohydroximol chloride, to which absolute methynol was added to yield the TPNO.

  11. Exact linear admittance of n+-n-n+ semiconductor structures

    NASA Astrophysics Data System (ADS)

    Eranen, S.; Sinkkonen, J.

    1985-10-01

    With the self-consistent solution of the linearized Boltzmann equation in the relaxation-time approximation for a spatially inhomogeneous electron system, the admittance of n+-n-n+ semiconductor structures is studied as a function of the length L of the moderately doped n region. It is shown that a one-dimensional treatment of the velocity space leads to the exact, analytical solution of the problem. In addition to the conventional admittance and the geometric capacitance of the n region, the equivalent circuit of the structure also includes the contact resistance and, as a new feature, the contact capacitance. For the strongly screened cases (L>>LD) the contact capacitance is approximately the permittivity ɛ of the n region divided by the Debye length LD and, further, becomes exactly equal to ɛL/6L2D in the weak-screening regime (LD>>L).

  12. Crystal structure of N,N,N',N',N'',N''-hexa-methyl-guanidinium cyanate 1.5-hydrate.

    PubMed

    Tiritiris, Ioannis; Kantlehner, Willi

    2015-12-01

    The title hydrated salt, C7H18N3 (+)·OCN(-).1.5H2O, was synthesized starting from N,N,N',N',N'',N''-hexa-methyl-guanidinium chloride by a twofold anion-exchange reaction. The asymmetric unit contains two cations, two cyanate anions and three water mol-ecules. One cation shows orientational disorder and two sets of N-atom positions were found related by a 60° rotation, with an occupancy ratio of 0.852 (6):0.148 (6). The C-N bond lengths in both guanidin-ium ions range from 1.329 (2) to 1.358 (10) Å, indicating double-bond character, pointing towards charge delocalization within the NCN planes. Strong O-H⋯N hydrogen bonds between the crystal water mol-ecules and the cyanate ions and strong O-H⋯O hydrogen bonds between the water mol-ecules are present, resulting in a two-dimensional hydrogen bonded network running parallel to the (001) plane. The hexa-methyl-guanidinium ions are packed in between the layers built up by water mol-ecules and cyanate ions.

  13. N-nitroso-N-methyldodecylamine and N-nitroso-N-methyltetradecylamine in hair-care products.

    PubMed

    Hecht, S S; Morrison, J B; Wenninger, J A

    1982-04-01

    N-Nitroso-N-methyldodecylamine and N-nitroso-N-methyltetradecylamine, which cause urinary bladder tumours in experimental animals, were detected in several hair-care products formulated with N,N-dimethyldodecylamine oxide. Quantitative determinations were made using a gas-liquid chromatograph interfaced with a thermal energy analyser and using [1-14C]N-nitroso-N-methyldodecylamine as an internal standard. The presence of the two nitrosamines was confirmed by high-pressure liquid chromatography with a thermal energy analyser as detector, by photolysis of samples and by combined gas chromatography-mass spectometry. To test the reproducibility of the method, a single shampoo was selected for replicate analysis and was found to contain 90 +/- 8 ppb N-nitroso-N-methyldodecylamine and 37 +/- 11 ppb N-nitroso-N-methyltetradecylamine. Levels of N-nitroso-N-methyldodecylamine in other hair-care products ranged from 11 to 873 ppb and those of n-nitroso-N-methyltetradecylamine from 8 to 254 ppb.

  14. Instantons and Large N

    NASA Astrophysics Data System (ADS)

    Mariño, Marcos

    2015-09-01

    Preface; Part I. Instantons: 1. Instantons in quantum mechanics; 2. Unstable vacua in quantum field theory; 3. Large order behavior and Borel summability; 4. Non-perturbative aspects of Yang-Mills theories; 5. Instantons and fermions; Part II. Large N: 6. Sigma models at large N; 7. The 1=N expansion in QCD; 8. Matrix models and matrix quantum mechanics at large N; 9. Large N QCD in two dimensions; 10. Instantons at large N; Appendix A. Harmonic analysis on S3; Appendix B. Heat kernel and zeta functions; Appendix C. Effective action for large N sigma models; References; Author index; Subject index.

  15. N-Nitroso-di-n-butylamine

    Integrated Risk Information System (IRIS)

    N - Nitroso - di - n - butylamine ; CASRN 924 - 16 - 3 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for

  16. First principles study of the ignition mechanism for hypergolic bipropellants: N,N,N',N'-tetramethylethylenediamine (TMEDA) and N,N,N',N'-tetramethylmethylenediamine (TMMDA) with nitric acid.

    PubMed

    Liu, Wei-Guang; Dasgupta, Siddharth; Zybin, Sergey V; Goddard, William A

    2011-05-26

    We report quantum mechanics calculations (B3LYP flavor of density functional theory) to determine the chemical reaction mechanism underlying the hypergolic reaction of pure HNO(3) with N,N,N',N'-tetramethylethylenediamine (TMEDA) and N,N,N',N'-tetramethylmethylenediamine (TMMDA). TMEDA and TMMDA are dimethyl amines linked by two CH(2) groups or one CH(2) group, respectively, but ignite very differently with HNO(3). We explain this dramatic difference in terms of the role that N lone-pair electrons play in activating adjacent chemical bonds. We identify two key atomistic level factors that affect the ignition delay: (1) The exothermicity for formation of the dinitrate salt from TMEDA or TMMDA. With only a single CH(2) group between basic amines, the diprotonation of TMMDA results in much stronger electrostatic repulsion, reducing the heat of dinitrate salt formation by 6.3 kcal/mol. (2) The reaction of NO(2) with TMEDA or TMMDA, which is the step that releases the heat and reactive species required to propagate the reaction. Two factors of TMEDA promote the kinetics by providing routes with low barriers to oxidize the C: (a) formation of a stable intermediate with a C-C double bond and (b) the lower bond energy for breaking the C-C single bond (by 18 kcal/mol comparing to alkane) between two amines. Both factors would decrease the ignition delay for TMEDA versus TMMDA. The same factors also explain the shorter ignition delay of 1,4-dimethylpiperazine (DMPipZ) versus 1,3,5-trimethylhexahydro-1,3,5-triazine (TMTZ). These results indicate that TMEDA and DMPipZ are excellent green replacements for hydrazines as the fuel in bipropellants.

  17. Thermodynamic characteristics of protolytic equilibria of hexamethylenediamine-N,N,N',N'-tetraacetic acid

    NASA Astrophysics Data System (ADS)

    Gridchin, S. N.; Pyreu, D. F.

    2011-04-01

    The heats of dissociation of betaine groups of hexamethylenediamine-N,N,N',N'-tetraacetic acid (H4L) at 298.15 K and the ionic strengths of 0.1, 0.5, and 1.0 (KNO3) were determined by direct calorimetry. The standard thermodynamic characteristics of the ptotolytic equilidria of H4L were calculated using the results from thermochemical and potentiometric measurements made under identical test conditions.

  18. Effect of moisture on corrosion of Ni-based alloys in molten alkali fluoride FLiNaK salt environments

    NASA Astrophysics Data System (ADS)

    Ouyang, Fan-Yi; Chang, Chi-Hung; You, Bo-Chien; Yeh, Tsung-Kuang; Kai, Ji-Jung

    2013-06-01

    We investigated the corrosion characteristics on several selected alloys at 600 and 700 °C in FLiNaK molten salts with different moisture contents. Hastelloys-N and Hastelloys-B3 exhibited better corrosion resistances, while Haynes 263 showed the poorest corrosion resistance. The mass loss of the tested alloys is primarily determined by the purity of FLiNaK salts; however, the effect of temperature becomes more important on the mass loss of the tested alloys in the non-purified FLiNaK salts. When the residual moisture is present in the FLiNaK salts, the mass losses of the tested alloys varied linearly with original Cr content plus one-third of Mo content. The results of structural characterization revealed that the tested alloys in the FLiNaK salts with higher moisture content would aggravate intergranular corrosion and pitting.

  19. 40 CFR 721.10056 - Benzenemethanaminium, N-(3-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...)-N,N-dimethyl-, N-soya acyl derivs., chlorides. 721.10056 Section 721.10056 Protection of Environment...-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides. (a) Chemical substance and significant new uses...-dimethyl-, N-soya acyl derivs., chlorides (PMN P-03-47; CAS No. 90194-13-1) is subject to reporting...

  20. 40 CFR 721.10056 - Benzenemethanaminium, N-(3-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...)-N,N-dimethyl-, N-soya acyl derivs., chlorides. 721.10056 Section 721.10056 Protection of Environment...-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides. (a) Chemical substance and significant new uses...-dimethyl-, N-soya acyl derivs., chlorides (PMN P-03-47; CAS No. 90194-13-1) is subject to reporting...

  1. 40 CFR 721.10056 - Benzenemethanaminium, N-(3-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...)-N,N-dimethyl-, N-soya acyl derivs., chlorides. 721.10056 Section 721.10056 Protection of Environment...-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides. (a) Chemical substance and significant new uses...-dimethyl-, N-soya acyl derivs., chlorides (PMN P-03-47; CAS No. 90194-13-1) is subject to reporting...

  2. 40 CFR 721.10056 - Benzenemethanaminium, N-(3-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...)-N,N-dimethyl-, N-soya acyl derivs., chlorides. 721.10056 Section 721.10056 Protection of Environment...-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides. (a) Chemical substance and significant new uses...-dimethyl-, N-soya acyl derivs., chlorides (PMN P-03-47; CAS No. 90194-13-1) is subject to reporting...

  3. 40 CFR 721.10056 - Benzenemethanaminium, N-(3-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...)-N,N-dimethyl-, N-soya acyl derivs., chlorides. 721.10056 Section 721.10056 Protection of Environment...-aminopropyl)-N,N-dimethyl-, N-soya acyl derivs., chlorides. (a) Chemical substance and significant new uses...-dimethyl-, N-soya acyl derivs., chlorides (PMN P-03-47; CAS No. 90194-13-1) is subject to reporting...

  4. "N" is for Now

    ERIC Educational Resources Information Center

    Briggs, Linda L.

    2008-01-01

    The leap in wireless LAN standards to 802.11n is a WiFi upgrade so new it has not yet garnered final approval from the standards committee. Although that approval will not come until next year (vendors are currently building to a "pre-n" standard), there are plenty of notebook computers out there capable of running 802.11n. That means students…

  5. Thermodynamic characteristics of the protolytic equilibria of tetramethylenediamine- N,N,N', N'-tetraacetic acid

    NASA Astrophysics Data System (ADS)

    Gridchin, S. N.; Nikol'skii, V. M.

    2014-04-01

    The stepwise dissociation constants of tetramethylenediamine- N,N,N', N'-tetraacetic acid (H4L) are determined by means of potentiometry at 298.15 K and ionic strength values of 0.1, 0.5, and 1.0 (KNO3). The heat effects of the dissociation of the betaine groups of the complexone are measured by direct calorimetry. The standard thermodynamic characteristics of the protolytic equilibria of H4L are calculated via combined use of the results from thermochemical and potentiometric studies performed under identical experimental conditions. Our results are compared with the corresponding data on relative compounds.

  6. Crystal structure of N-[3-(di-methyl-aza-nium-yl)prop-yl]-N',N',N'',N''-tetra-methyl-N-(N,N,N',N'-tetra-methyl-form-am-id-in-ium-yl)-guanidinium dibromide hydroxide monohydrate.

    PubMed

    Tiritiris, Ioannis; Kantlehner, Willi

    2015-12-01

    The asymmetric unit of the title hydrated salt, C15H37N6 (3+)·2Br(-)·OH(-)·H2O, contains one cation, three partial-occupancy bromide ions, one hydroxide ion and one water mol-ecule. Refinement of the site-occupancy factors of the three disordered bromide ions converges with occupancies 0.701 (2), 0.831 (2) and 0.456 (2) summing to approximately two bromide ions per formula unit. The structure was refined as a two-component inversion twin with volume fractions 0.109 (8):0.891 (8) for the two domains. The central C3N unit of the bis-amidinium ion is linked to the aliphatic propyl chain by a C-N single bond. The other two bonds in this unit have double-bond character as have the four C-N bonds to the outer NMe2 groups. In contrast, the three C-N bonds to the central N atom of the (di-methyl-aza-nium-yl)propyl group have single-bond character. Delocalization of the two positive charges occurs in the N/C/N and C/N/C planes, while the third positive charge is localized on the di-methyl-ammonium group. The crystal structure is stabilized by O-H⋯O, N-H⋯Br, O-H⋯Br and C-H⋯Br hydrogen bonds, forming a three-dimensional network.

  7. 40 CFR 721.9957 - N-Nitroso-N-methylurethane.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false N-Nitroso-N-methylurethane. 721.9957... Substances § 721.9957 N-Nitroso-N-methylurethane. (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance N-nitroso-N-methylurethane (CAS No. 615-53-2) is subject to...

  8. 40 CFR 721.9957 - N-Nitroso-N-methylurethane.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false N-Nitroso-N-methylurethane. 721.9957... Substances § 721.9957 N-Nitroso-N-methylurethane. (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance N-nitroso-N-methylurethane (CAS No. 615-53-2) is subject to...

  9. 40 CFR 721.9957 - N-Nitroso-N-methylurethane.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false N-Nitroso-N-methylurethane. 721.9957... Substances § 721.9957 N-Nitroso-N-methylurethane. (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance N-nitroso-N-methylurethane (CAS No. 615-53-2) is subject to...

  10. 40 CFR 721.9957 - N-Nitroso-N-methylurethane.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false N-Nitroso-N-methylurethane. 721.9957... Substances § 721.9957 N-Nitroso-N-methylurethane. (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance N-nitroso-N-methylurethane (CAS No. 615-53-2) is subject to...

  11. 40 CFR 721.9957 - N-Nitroso-N-methylurethane.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false N-Nitroso-N-methylurethane. 721.9957... Substances § 721.9957 N-Nitroso-N-methylurethane. (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance N-nitroso-N-methylurethane (CAS No. 615-53-2) is subject to...

  12. Radiación

    NASA Video Gallery

    Fuera del capullo protector de la atmósfera terrestre, el universo está plagado de radiación dañina. Los astronautas que viven y trabajan en el espacio están expuestos no sólo a los rayos ultraviol...

  13. Eastman N. Jacobs

    NASA Technical Reports Server (NTRS)

    1945-01-01

    Sylvanus Albert Reed Award: Eastman N. Jacobs: In 1937, Eastman N. Jacobs, one of Langley's most adventurous researchers, received the Sylvanus Albert Reed Award for his contributions to the aerodynamic improvement of airfoils. Published in James R. Hansen, Engineer in Charge, NASA SP- 4305, p. 106.

  14. Neuropharmacology of N,N-dimethyltryptamine.

    PubMed

    Carbonaro, Theresa M; Gatch, Michael B

    2016-09-01

    N,N-dimethyltryptamine (DMT) is an indole alkaloid widely found in plants and animals. It is best known for producing brief and intense psychedelic effects when ingested. Increasing evidence suggests that endogenous DMT plays important roles for a number of processes in the periphery and central nervous system, and may act as a neurotransmitter. This paper reviews the current literature of both the recreational use of DMT and its potential roles as an endogenous neurotransmitter. Pharmacokinetics, mechanisms of action in the periphery and central nervous system, clinical uses and adverse effects are also reviewed. DMT appears to have limited neurotoxicity and other adverse effects except for intense cardiovascular effects when administered intravenously in large doses. Because of its role in nervous system signaling, DMT may be a useful experimental tool in exploring how the brain works, and may also be a useful clinical tool for treatment of anxiety and psychosis.

  15. N Reactor hydrogen control

    SciTech Connect

    Shuford, D.H.; Kripps, L.J.

    1988-08-01

    Following the accident at the Chernobyl nuclear power reactor in the Soviet Union, a number of reviews were conducted of the N Reactor. Hydrogen generation during postulates severe accidents and the possibility of resulting hydrogen deflagrations/detonations that could affect confinement integrity were issues raised in several reviews, along with recommendations for adding hydrogen mitigation features. To respond to these reviews, an N Reactor Safety Enhancement Program and a subsequent Accelerated Safety Enhancement Program were initiated to address all post-Chernobyl N Reactor review findings. The Safety Enhancement Program and Accelerated Safety Enhancement Program efforts involving hydrogen control included the following: Calculate the potential hydrogen source for a range of severe accidents at the N Reactor to establish an acceptable design basis for the hydrogen mitigation system; Analyze the N Reactor confinement hydrogen mixing capability to identify areas of concern and to the verify effectiveness of the hydrogen mitigation system; Select, design, and construct a hydrogen mitigation system to enhance the N Reactor capability to accommodate possible hydrogen generation from postulated severe accidents; Provide post-accident hydrogen monitoring as an operator aid in assessing confinement conditions. In additions, it was necessary to verify that incorporation of the hydrogen mitigation system had no adverse impact N Reactor safety (e.g., radiological consequence analyses). 77 refs., 25 figs., 10 tabs.

  16. Pulsed terahertz emission from GaN/InN heterostructure

    NASA Astrophysics Data System (ADS)

    Reklaitis, Antanas

    2011-11-01

    Dynamics of the electron-hole plasma excited by the femtosecond optical pulse in wurtzite GaN/InN heterostructure is investigated by Monte Carlo simulations. The GaN/InN heterostructure for pulsed terahertz emission is suggested. The results of Monte Carlo simulations show that the power of terahertz emission from the GaN/InN heterostructure exceeds the power of terahertz emission from the surface of InN by one order of magnitude.

  17. Weyl n-Algebras

    NASA Astrophysics Data System (ADS)

    Markarian, Nikita

    2017-03-01

    We introduce Weyl n-algebras and show how their factorization complex may be used to define invariants of manifolds. In the appendix, we heuristically explain why these invariants must be perturbative Chern-Simons invariants.

  18. GaN HEMTs

    NASA Astrophysics Data System (ADS)

    Anderson, Jonathan W.; Lee, Kyoung-Keun; Piner, Edwin L.

    2012-03-01

    Gallium nitride (GaN) has enormous potential for applications in high electron mobility transistors (HEMTs) used in RF and power devices. Intrinsic device properties such as high electron mobility, high breakdown voltage, very high current density, electron confinement in a narrow channel, and high electron velocity in the 2-dimensional electron gas of the HEMT structure are due in large part to the wide band gap of this novel semiconductor material system. This presentation discusses the properties of GaN that make it superior to other semiconductor materials, and outlines the research that will be undertaken in a new program at Texas State University to advance GaN HEMT technology. This program's aim is to further innovate the exceptional performance of GaN through improved material growth processes and epitaxial structure design.

  19. Human psychopharmacology of N,N-dimethyltryptamine.

    PubMed

    Strassman, R J

    1996-01-01

    We generated dose-response data for the endogenous and ultra-short-acting hallucinogen, N,N-dimethyltryptamine (DMT), in a cohort of experienced hallucinogen users, measuring multiple biological and psychological outcome measures. Subjective responses were quantified with a new rating scale, the HRS, which provided better resolution of dose effects than did the biological variables. A tolerance study then was performed, in which volunteers received four closely spaced hallucinogenic doses of DMT. Subjective responses demonstrated no tolerance, while biological measures were inconsistently reduced over the course of the sessions. Thus, DMT remains unique among classic hallucinogens in its inability to induce tolerance to its psychological effects. To assess the role of the 5-HT1A site in mediating DMT's effects, a pindolol pre-treatment study was performed. Pindolol significantly increased psychological responses to DMT, suggesting a buffering effect of 5-HT1A agonism on 5-HT2-mediated psychedelic effects. These data are opposite to those described in lower animal models of hallucinogens' mechanisms of action.

  20. Electron states at electrolyte/n-GaN and electrolyte/n-InGaN interfaces

    SciTech Connect

    Rudinsky, M. E. Gutkin, A. A.; Brunkov, P. N.

    2012-06-15

    The differential capacitance and differential active conductance of rectifying contacts of n-GaN and n-In{sub x}Ga{sub 1-x}N (x Almost-Equal-To 0.15) with an electrolyte (0.2 M aqueous solutions of NaOH, NaCl, or HCl) have been studied. It was found that electron states with energies corresponding to the upper half of the energy gap of a semiconductor exist at the interface between these semiconductors and a NaOH solution. The density and characteristic recharging time of states noticeably contributing to the differential capacitance and differential active conductance at probe-voltage frequencies of 0.3-1 kHz grow with their binding energy and, for states lying at 0.15-0.3 eV below the conduction-band bottom of n-GaN, fall within the ranges 10{sup 12}-2 Multiplication-Sign 10{sup 13} cm{sup -2} eV{sup -1} and 10{sup -4}-10{sup -2} s, respectively. For contacts with NaCl and HCl solutions, there are no states of this kind. It is assumed that the observed states are related to the adsorption of hydroxyl groups.

  1. 40 CFR 721.10174 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. 721.10174 Section 721.10174 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. (a) Chemical substance...-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts (PMN...

  2. 40 CFR 721.10174 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. 721.10174 Section 721.10174 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. (a) Chemical substance...-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts (PMN...

  3. 40 CFR 721.10174 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. 721.10174 Section 721.10174 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. (a) Chemical substance...-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts (PMN...

  4. 40 CFR 721.10174 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. 721.10174 Section 721.10174 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. (a) Chemical substance...-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts (PMN...

  5. 40 CFR 721.7270 - 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl derivs., chloride.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-trimethyl-N-soya acyl derivs., chloride. 721.7270 Section 721.7270 Protection of Environment ENVIRONMENTAL...-soya acyl derivs., chloride. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl...

  6. 40 CFR 721.7270 - 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl derivs., chloride.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-trimethyl-N-soya acyl derivs., chloride. 721.7270 Section 721.7270 Protection of Environment ENVIRONMENTAL...-soya acyl derivs., chloride. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl...

  7. N-methylated tryptamine derivatives in citrus genus plants: identification of N,N,N-trimethyltryptamine in bergamot.

    PubMed

    Servillo, Luigi; Giovane, Alfonso; Balestrieri, Maria Luisa; Cautela, Domenico; Castaldo, Domenico

    2012-09-19

    The occurrence of N-methylated tryptamine derivatives in bergamot plant (Citrus bergamia Risso et Poit) is reported for the first time. Interestingly, the most abundant of these substances is N,N,N-trimethyltryptamine, which has not been previously identified in any citrus plant. The N-methylated tryptamine derivatives were identified and quantitated in leaves, peel, juice, and seeds by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry. N,N,N-Trimethyltryptamine was confirmed by MS(3) and comparison with the synthesized authentic standard. In addition, the study of the distribution of tryptophan, tryptamine, N-methyltryptamine, N,N-dimethyltryptamine, and N,N,N-trimethyltryptamine indicated that these compounds are differently expressed in the various tissues of the bergamot plant. Intriguingly, chemically synthesized N,N,N-trimethyltryptamine was reported to possess nicotine-like activity being a stimulant of parasympathetic ganglia by exerting its action on acetylcholine receptors. On this basis, the identification of N,N,N-trimethyltryptamine at a relatively high level in leaves suggests a possible role in a physiological mechanism of plant defense.

  8. African N Assessment

    NASA Astrophysics Data System (ADS)

    Bekunda, M.; Galford, G. L.; Hickman, J. E.; Palm, C.

    2011-12-01

    Africa's smallholder agricultural systems face unique challenges in planning for reducing poverty, concurrent with adaptation and mitigation to climate change. At continental level, policy seeks to promote a uniquely African Green Revolution to increase crop yields and food production, and improve local livelihoods. However, the consequences on the environment and climate are not clear; these pro-economic development measures should be linked to climate change adaptation and mitigation measures, and research is required to help achieve these policy proposals by identifying options, and testing impacts. In particular, increased nitrogen (N) inputs are essential for increasing food production in Africa, but are accompanied by inevitable increases in losses to the environment. These losses appear to be low at input levels promoted in agricultural development programs, while the increased N inputs both increase current food production and appear to reduce the vulnerability of food production to changes in climate. We present field and remote sensing evidence from Malawi that subsidizing improved seed and fertilizers increases resilience to drought without adding excess N to the environment. In Kenya, field research identified thresholds in N2O losses, where emissions are very low at fertilization rates of less than 200 kg ha-1. Village-scale models have identified potential inefficiencies in the food production process where the largest losses of reactive N occur, and which could be targeted to reduce the amount of N released to the environment. We further review some on-going research activities and progress in Africa that compare different methods of managing resources that target resilience in food production and adaptation to climate change, using nutrient N as an indicator, while evaluating the effects of these resource management practices on ecosystems and the environment.

  9. N-methylated derivatives of tyramine in citrus genus plants: identification of N,N,N-trimethyltyramine (candicine).

    PubMed

    Servillo, Luigi; Giovane, Alfonso; D'Onofrio, Nunzia; Casale, Rosario; Cautela, Domenico; Ferrari, Giovanna; Balestrieri, Maria Luisa; Castaldo, Domenico

    2014-03-26

    The distribution of tyramine and its methylated derivatives, N-methyltyramine and N,N-dimethyltyramine, was investigated in tissue parts (leaves and fruits) of several plants of Citrus genus by liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). In the course of our study we discovered the occurrence of N,N,N-trimethyltyramine in all citrus plants examined. This quaternary ammonium compound, known to act in animals as a neurotoxin, was recognized and characterized by mass spectrometric analysis. The substance, never described before in the Citrus genus, is also known as candicine or maltoxin. Results indicate that N,N,N-trimethyltyramine is consistently expressed in leaves of clementine, bitter orange, and lemon. Conversely, low levels were found in the leaves of orange, mandarin, chinotto (Citrus myrtifolia), bergamot, citron, and pomelo. In the edible part of the fruits, N,N,N-trimethyltyramine was found at trace levels.

  10. (μ-2-Pyridine-aldazine-κN,N':N'',N''')bis-[bis-(N,N-di-n-propyl-dithio-carbamato-κS,S')cadmium(II)].

    PubMed

    Poplaukhin, Pavel; Tiekink, Edward R T

    2008-08-16

    The dinuclear centrosymmetric title compound, [Cd(2)(C(7)H(14)NS(2))(4)(C(12)H(10)N(4))], features a tetra-dentate 2-pyridine-aldazine ligand that chelates two Cd centres. The coordination geometry for Cd is distorted octa-hedral based on a cis-N(2)S(4) donor set. In the crystal structure, mol-ecules are connected into a supra-molecular chain aligned along the a direction via C-H⋯S and C-H⋯π contacts, and by π-π contacts [centroid-to-centroid distance 3.5708 (15) Å]. The n-propyl groups are each disordered, one equally over two sites and the other with a site-occupancy factor of 0.618 (8) for the major component.

  11. 40 CFR 721.10055 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. 721.10055 Section 721.10055 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. (a) Chemical substance and...-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts (PMN P-03-46; CAS No. 136504-87-5) is subject...

  12. 40 CFR 721.10055 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. 721.10055 Section 721.10055 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. (a) Chemical substance and...-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts (PMN P-03-46; CAS No. 136504-87-5) is subject...

  13. n-Butanol

    Integrated Risk Information System (IRIS)

    n - Butanol ; CASRN 71 - 36 - 3 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effect

  14. The "N" Word.

    ERIC Educational Resources Information Center

    Zirkel, Perry A.

    1999-01-01

    In a lawsuit involving classroom and literary racial epithets, the Ninth Circuit Court remanded the racial-harassment claim, not the book-removal claim. The ultimate outcome awaits trial; the court's Solomonic decision needs further testing. Meanwhile, the "N" word is a no-no for teachers and students, but not necessarily for books. (MLH)

  15. n-Hexane

    Integrated Risk Information System (IRIS)

    n - Hexane ; CASRN 110 - 54 - 3 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effect

  16. n-Heptane

    Integrated Risk Information System (IRIS)

    n - Heptane ; CASRN 142 - 82 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effec

  17. N-Nitrosopyrrolidine

    Integrated Risk Information System (IRIS)

    N - Nitrosopyrrolidine ; CASRN 930 - 55 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcino

  18. N-Nitrosodimethylamine

    Integrated Risk Information System (IRIS)

    N - Nitrosodimethylamine ; CASRN 62 - 75 - 9 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcin

  19. N-Nitrosodiethanolamine

    Integrated Risk Information System (IRIS)

    N - Nitrosodiethanolamine ; CASRN 1116 - 54 - 7 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncar

  20. N-Nitrosodiethylamine

    Integrated Risk Information System (IRIS)

    N - Nitrosodiethylamine ; CASRN 55 - 18 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcino

  1. N-Nitrosodiphenylamine

    Integrated Risk Information System (IRIS)

    N - Nitrosodiphenylamine ; CASRN 86 - 30 - 6 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcin

  2. Genotoxicity analysis of N,N-dimethylaniline and N,N-dimethyl-p-toluidine

    SciTech Connect

    Taningher, M. ); Bonatti, S. ); Pasquini, R. )

    1993-01-01

    N,N-Dimethylaniline (DMA, CAS No. 121-69-7) and N,N-dimethyl-p-toluidine (DMPT, CAS No. 99-97-8) belong to the N-dialkylaminoaromatics, a chemical class structurally alerting to DNA reactivity. Their applications may be industrial (dye and pesticide intermediates, polymerizing agents) and surgical (polymerization accelerations for the manufacture of bone cements and prosthetic devices), thus implying heterogeneous types of human exposure. Findings of carcinogenicity in rodents and some nonexhaustive genotoxicity data are available for DMA, but no information is available on DMPT concerning either carcinogenicity or any kind of genetic toxicity. To investigate their mechanism of action and mutagenic/carcinogenic potential, DMA and DMPT were analyzed for complementary genotoxicity endpoints, namely, gene mutation in Salmonella (Ames test), structural and numerical chromosome aberrations in hamster V79 cells (micronucleus test, matched with an immunofluorescent staining for kinetochore proteins), and in vivo DNA damage in mouse and rat liver (alkaline DNA elution test). The results essentially indicate that both chemicals are chromosome damaging agents. Indeed, at the maximum nontoxic doses, they proved nonmutagenic in Salmonella (although their toxicity did not allow concentrations > 70 [mu]g/plate to be tested) and weakly positive in inducing DNA damage (increases in DNA elution rates at most [approximately]2.4 times control value). Conversely, they proved clearly positive in inducing numerical chromosome alterations, with dose-dependent increases up to more than five times the control value for DMPT. At the highest dose tested, both chemicals also showed a significant clastogenic effect. 28 refs., 4 tabs.

  3. Noncompetitive inhibition of indolethylamine-N-methyltransferase by N,N-dimethyltryptamine and N,N-dimethylaminopropyltryptamine.

    PubMed

    Chu, Uyen B; Vorperian, Sevahn K; Satyshur, Kenneth; Eickstaedt, Kelsey; Cozzi, Nicholas V; Mavlyutov, Timur; Hajipour, Abdol R; Ruoho, Arnold E

    2014-05-13

    Indolethylamine-N-methyltransferase (INMT) is a Class 1 transmethylation enzyme known for its production of N,N-dimethyltryptamine (DMT), a hallucinogen with affinity for various serotonergic, adrenergic, histaminergic, dopaminergic, and sigma-1 receptors. DMT is produced via the action of INMT on the endogenous substrates tryptamine and S-adenosyl-l-methionine (SAM). The biological, biochemical, and selective small molecule regulation of INMT enzyme activity remain largely unknown. Kinetic mechanisms for inhibition of rabbit lung INMT (rabINMT) by the product, DMT, and by a new novel tryptamine derivative were determined. After Michaelis-Menten and Lineweaver-Burk analyses had been applied to study inhibition, DMT was found to be a mixed competitive and noncompetitive inhibitor when measured against tryptamine. The novel tryptamine derivative, N-[2-(1H-indol-3-yl)ethyl]-N',N'-dimethylpropane-1,3-diamine (propyl dimethyl amino tryptamine or PDAT), was shown to inhibit rabINMT by a pure noncompetitive mechanism when measured against tryptamine with a Ki of 84 μM. No inhibition by PDAT was observed at 2 mM when it was tested against structurally similar Class 1 methyltransferases, such as human phenylethanolamine-N-methyltransferase (hPNMT) and human nicotinamide-N-methyltransferase (hNNMT), indicating selectivity for INMT. The demonstration of noncompetitive mechanisms for INMT inhibition implies the presence of an inhibitory allosteric site. In silico analyses using the computer modeling software Autodock and the rabINMT sequence threaded onto the human INMT (hINMT) structure (Protein Data Bank entry 2A14 ) identified an N-terminal helix-loop-helix non-active site binding region of the enzyme. The energies for binding of DMT and PDAT to this region of rabINMT, as determined by Autodock, were -6.34 and -7.58 kcal/mol, respectively. Assessment of the allosteric control of INMT may illuminate new biochemical pathway(s) underlying the biology of INMT.

  4. The pK(a) values of N,N,N',N'-tetrakis-(2-hydroxypropyl)ethylenediamine.

    PubMed

    McMahon, R; Brennan, M; Glennon, J D

    1986-11-01

    Aqueous solutions of the industrially important chelating agent N,N,N',N'-tetrakis(2-hydroxypropyl)ethylenediamine exhibit basic properties. The proton dissociation constants were determined to be 8.99 +/- 0.04 (pK(1)) and 4.30 +/- 0.04 (pK(2)) by potentiometric titration at 25 degrees in 0.15M sodium chloride.

  5. InAlN/AlN/GaN heterostructures for high electron mobility transistors

    NASA Astrophysics Data System (ADS)

    Usov, S. O.; Sakharov, A. V.; Tsatsulnikov, A. F.; Lundin, V. W.; Zavarin, E. E.; Nikolaev, A. E.; Yagovkina, M. A.; Zemlyakov, V. E.; Egorkin, V. I.; Ustinov, V. M.

    2016-08-01

    The results of development of InAlN/AlN/GaN heterostructures, grown on sapphire substrates by metal-organic chemical vapour deposition, and high electron mobility transistors (HEMTs) based on them are presented. The dependencies of the InAlN/AlN/GaN heterostructure properties on epitaxial growth conditions were investigated. The optimal indium content and InAlN barrier layer thicknesses of the heterostructures for HEMT s were determined. The possibility to improve the characteristics of HEMTs by in-situ passivation by Si3N4 thin protective layer deposited in the same epitaxial process was demonstrated. The InAlN/AlN/GaN heterostructure grown on sapphire substrate with diameter of 100 mm were obtained with sufficiently uniform distribution of sheet resistance. The HEMTs with saturation current of 1600 mA/mm and transconductance of 230 mS/mm are demonstrated.

  6. Etudes on 1/N

    NASA Astrophysics Data System (ADS)

    Starinets, Andrei Olegovich

    A number of problems in string theory and lattice statistical mechanics is studied using the large N approximation, with N being the dimension of the fundamental representation of the underlying symmetry algebra. As the first problem, the absorption of a minimally coupled massless scalar in the gravitational background created by a stack of near-extremal black three-branes is considered. The low-temperature asymptotic expansion and the high-temperature perturbative expansion are obtained. A field-theoretical calculation of the absorption cross section in the brane's world-volume theory is also performed. As an application, the shear viscosity of a strongly coupled Yang-Mills plasma is computed. In the second problem, we study supergravity solutions with two asymptotically Anti de Sitter regions which are conjectured to describe the renormalization group flow of a four-dimensional field theory from a UV fixed point to an interacting IR fixed point. We show that, in the UV (IR) limit, the two-point function of a minimally-coupled scalar field depends only on the UV (IR) region of the metric, asymptotic to AdS5 thus lending a support to the conjecture. In the third problem, monotonicity and other properties of the canonical c-function in some holographic duals of 4-d quantum field theories are investigated. The canonical c-function and its derivatives are related to the 5-d Green's function of the dual supergravity theory. In the fourth problem, we study solutions of the equations (Δ - λ)φ = 0 and (Δ - λ)2φ = 0 on the covering space C AdSd of the d-dimensional Anti de-Sitter space subject to various boundary conditions, and we analyze their connection to the unitary irreducible representations of SO (d - 1, 2). Finally, as the fifth problem, we compute the phase diagram in the N --> ∞ limit for lattice RPN-1, CPN-1 and QPN-1 σ- models with the quartic action, and more generally for mixed isovector/isotensor models. We show that the N = ∞ limit exhibits

  7. 40 CFR 721.10115 - 1-Hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 1-Hexadecanaminium, N,N-dibutyl-N-(2... New Uses for Specific Chemical Substances § 721.10115 1-Hexadecanaminium, N,N-dibutyl-N-(2... chemical substance identified as 1-hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1) (PMN...

  8. 40 CFR 721.10115 - 1-Hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false 1-Hexadecanaminium, N,N-dibutyl-N-(2... New Uses for Specific Chemical Substances § 721.10115 1-Hexadecanaminium, N,N-dibutyl-N-(2... chemical substance identified as 1-hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1) (PMN...

  9. 40 CFR 721.10595 - Octadecen-1-aminium, N-ethyl-N,N-dimethy-, ethyl sulfate (1:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Octadecen-1-aminium, N-ethyl-N,N... Significant New Uses for Specific Chemical Substances § 721.10595 Octadecen-1-aminium, N-ethyl-N,N-dimethy... chemical substance identified as octadecen-1-aminium, N-ethyl-N,N-dimethy-, ethyl sulfate (1:1) (PMN...

  10. 40 CFR 721.10115 - 1-Hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false 1-Hexadecanaminium, N,N-dibutyl-N-(2... New Uses for Specific Chemical Substances § 721.10115 1-Hexadecanaminium, N,N-dibutyl-N-(2... chemical substance identified as 1-hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1) (PMN...

  11. 40 CFR 721.10115 - 1-Hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false 1-Hexadecanaminium, N,N-dibutyl-N-(2... New Uses for Specific Chemical Substances § 721.10115 1-Hexadecanaminium, N,N-dibutyl-N-(2... chemical substance identified as 1-hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1) (PMN...

  12. 40 CFR 721.10115 - 1-Hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false 1-Hexadecanaminium, N,N-dibutyl-N-(2... New Uses for Specific Chemical Substances § 721.10115 1-Hexadecanaminium, N,N-dibutyl-N-(2... chemical substance identified as 1-hexadecanaminium, N,N-dibutyl-N-(2-hydroxyethyl)-, bromide (1:1) (PMN...

  13. Ethyl N-phenyloxamate.

    PubMed

    García-Báez E, Efrén V; Gómez-Castro, Carlos Z; Höpfl, Herbert; Martínez-Martínez, Francisco J; Padilla-Martínez, Itzia I

    2003-10-01

    The oxamate group in the title compound, C(10)H(11)NO(3), is almost coplanar with the phenyl ring because of intramolecular hydrogen-bonding interactions, and the structure can be described as an anilide single bonded to an ethyl carboxylate group. The supramolecular structure is achieved through intermolecular hard N-H...O and soft C-H...X (X = O and phenyl) hydrogen-bonding interactions.

  14. Heats of Formation for CF(sub n) (n = 1 - 4), CF(sup +, sub n) (n = 1 - 4), and CF(sup -, sub n) (n = 1 - 3)

    NASA Technical Reports Server (NTRS)

    Ricca, Alessandra; Arnold, James (Technical Monitor)

    1998-01-01

    Accurate heats of formation are computed for CF(sub n) (n = 1 - 4), CF(sup +, sub n) (n = 1 - 4), and CF(sup -, sub n) (n = 1 - 3). The geometries and vibrational frequencies are determined at the B3LYP level of theory. The energetics are determined at the CCSD(T) level of theory. Basis set limit values are obtained by extrapolation. In those cases where the CCSD(T) calculations become prohibitively large, the basis set extrapolation is performed at the MP2 level. The temperature dependence of the heat of formation, heat capacity, and entropy are computed for the temperature range 300 to 4000 K and fit to a polynomial.

  15. Noncompetitive Inhibition of Indolethylamine-N-methyltransferase by N,N-Dimethyltryptamine and N,N-Dimethylaminopropyltryptamine

    PubMed Central

    2015-01-01

    Indolethylamine-N-methyltransferase (INMT) is a Class 1 transmethylation enzyme known for its production of N,N-dimethyltryptamine (DMT), a hallucinogen with affinity for various serotonergic, adrenergic, histaminergic, dopaminergic, and sigma-1 receptors. DMT is produced via the action of INMT on the endogenous substrates tryptamine and S-adenosyl-l-methionine (SAM). The biological, biochemical, and selective small molecule regulation of INMT enzyme activity remain largely unknown. Kinetic mechanisms for inhibition of rabbit lung INMT (rabINMT) by the product, DMT, and by a new novel tryptamine derivative were determined. After Michaelis–Menten and Lineweaver–Burk analyses had been applied to study inhibition, DMT was found to be a mixed competitive and noncompetitive inhibitor when measured against tryptamine. The novel tryptamine derivative, N-[2-(1H-indol-3-yl)ethyl]-N′,N′-dimethylpropane-1,3-diamine (propyl dimethyl amino tryptamine or PDAT), was shown to inhibit rabINMT by a pure noncompetitive mechanism when measured against tryptamine with a Ki of 84 μM. No inhibition by PDAT was observed at 2 mM when it was tested against structurally similar Class 1 methyltransferases, such as human phenylethanolamine-N-methyltransferase (hPNMT) and human nicotinamide-N-methyltransferase (hNNMT), indicating selectivity for INMT. The demonstration of noncompetitive mechanisms for INMT inhibition implies the presence of an inhibitory allosteric site. In silico analyses using the computer modeling software Autodock and the rabINMT sequence threaded onto the human INMT (hINMT) structure (Protein Data Bank entry 2A14) identified an N-terminal helix–loop–helix non-active site binding region of the enzyme. The energies for binding of DMT and PDAT to this region of rabINMT, as determined by Autodock, were −6.34 and −7.58 kcal/mol, respectively. Assessment of the allosteric control of INMT may illuminate new biochemical pathway(s) underlying the biology of INMT

  16. Exchange interactions and Curie temperatures of the tetrametal nitrides Cr₄N, Mn₄N, Fe₄N, Co₄N, and Ni₄N.

    PubMed

    Meinert, Markus

    2016-02-10

    The exchange interactions of Cr4N, Mn4N, Fe4N, Co4N, and Ni4N compounds with perovskite structure were calculated to obtain the Curie temperatures for these compounds from Monte Carlo calculations. Contrary to naíve expectation, the exchange interactions vary markedly among these five compounds. In Fe4N, the intra-sublattice interaction of the Fe 3c atoms is strongly negative, leading to a significant reduction of the Curie temperature. The calculated Curie temperatures are 291 K (Cr4N), 710 K (Mn4N), 668 K (Fe4N), 827 K (Co4N), and 121 K (Ni4N), in good agreement with experimental observations where available. The much lower Curie temperature of Ni4N compared to fcc Ni is explained on the basis of the exchange interactions.

  17. 14N15N detectability in Pluto’s atmosphere

    NASA Astrophysics Data System (ADS)

    Jessup, Kandis Lea; Gladstone, G. R.; Heays, A. N.; Gibson, S. T.; Lewis, B. R.; Stark, G.

    2013-11-01

    Based on the vapor pressure behavior of Pluto’s surface ices, Pluto’s atmosphere is expected to be predominantly composed of N2 gas. Measurement of the N2 isotopologue 15N/14N ratio within Pluto’s atmosphere would provide important clues to the evolution of Pluto’s atmosphere from the time of formation to its present state. The most straightforward way of determining the N2 isotopologue 15N/14N ratio in Pluto’s atmosphere is via spectroscopic observation of the 14N15N gas species. Recent calculations of the 80-100 nm absorption behavior of the 14N2 and 14N15N isotopologues by Heays et al. (Heays, A.N. et al. [2011]. J. Chem. Phys. 135, 244301), Lewis et al. (Lewis, B.R., Heays, A.N., Gibson, S.T., Lefebvre-Brion, H., Lefebvre, R. [2008]. J. Chem. Phys. 129, 164306); Lewis et al. (Lewis, B.R., Gibson, S.T., Zhang, W., Lefebvre-Brion, H., Robbe, J.-M. [2005]. J. Chem. Phys. 122, 144302), and Haverd et al. (Haverd, V.E., Lewis, B.R., Gibson, S.T., Stark, G. [2005]. J. Chem. Phys. 123, 214304) show that the peak magnitudes of the 14N2 and 14N15N absorption bandhead cross-sections are similar, but the locations of the bandhead peaks are offset in wavelength by ∼0.05-0.1 nm. These offsets make the segregation of the 14N2 and 14N15N absorption signatures possible. We use the most recent N2 isotopologue absorption cross-section calculations and the atmospheric density profiles resulting from photochemical models developed by Krasnopolsky and Cruickshank (Krasnopolsky, V.A., Cruickshank, D.P. [1999]. J. Geophys. Res. 104, 21979-21996) to predict the level of solar light that will be transmitted through Pluto’s atmosphere as a function of altitude during a Pluto solar occultation. We characterize the detectability of the isotopic absorption signature per altitude assuming 14N15N concentrations ranging from 0.1% to 2% of the 14N2 density and instrumental spectral resolutions ranging from 0.01 to 0.3 nm. Our simulations indicate that optical depth of unity is

  18. Quantitation of N,N,N',N'-tetrakis (2-hydroxypropyl)-ethylenediamine in plasma by gas chromatography.

    PubMed

    Dunphy, M J; Smith, D J

    1989-03-24

    A wide-bore capillary gas chromatographic method with nitrogen-selective thermionic detection is described for the quantitative analysis of N,N,N',N'-tetrakis (2-hydroxypropyl)ethylenediamine (Quadrol) in plasma. N,N,N',N'-tetrakis (2-hydroxybutyl)ethylenediamine is used as an internal standard. Rat or human plasma samples (0.5 ml) are mixed with internal standard, adjusted to alkaline pH and subjected to a single extraction with dichloromethane. Quadrol recovery from plasma typically exceeds 90%. The method is linear over the range 1.0-50 micrograms/ml. The working detection limit is 0.5 microgram/ml and the analysis time is under 7 min. The procedure has been used to obtain plasma concentration versus time data for the evaluation of Quadrol pharmacokinetics in rats.

  19. Impact ionization in N-polar AlGaN/GaN high electron mobility transistors

    SciTech Connect

    Killat, N. E-mail: Martin.Kuball@bristol.ac.uk; Uren, M. J.; Kuball, M. E-mail: Martin.Kuball@bristol.ac.uk; Keller, S.; Kolluri, S.; Mishra, U. K.

    2014-08-11

    The existence of impact ionization as one of the open questions for GaN device reliability was studied in N-polar AlGaN/GaN high electron mobility transistors. Electroluminescence (EL) imaging and spectroscopy from underneath the device gate contact revealed the presence of hot electrons in excess of the GaN bandgap energy even at moderate on-state bias conditions, enabling impact ionization with hole currents up to several hundreds of pA/mm. The detection of high energy luminescence from hot electrons demonstrates that EL analysis is a highly sensitive tool to study degradation mechanisms in GaN devices.

  20. A complex containing three different kinds of Ru-N bonds: ethoxydinitronitrosyl(N,N,N',N'-tetramethylethylenediamine-kappa2N,N')ruthenium(II).

    PubMed

    Albores, Pablo; Chaia, Zulema D; Baraldo, Luis; Castellano, Eduardo E; Piro, Oscar E

    2002-04-01

    The octahedral title compound, [Ru(C(2)H(5)O)(NO)(NO(2))(2)(C(6)H(16)N(2))], crystallizes in the rhombohedral space group P3(1) with an ethoxy ligand axially coordinated trans to the nitrosyl ligand. The RuII ion is equatorially coordinated by a tetramethylethylenediamine group acting as a bidentate ligand, and to two nitro moieties whose planes are tilted with respect to the mean equatorial plane. Each nitrogen ligand bonded to the metallic centre has a different hybridization state.

  1. 40 CFR 180.1130 - N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false N-(n-octyl)-2-pyrrolidone and N-(n... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1130 N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a tolerance....

  2. 40 CFR 721.10174 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. 721.10174 Section 721.10174 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-peanut-oil acyl derivs., inner salts. (a) Chemical...

  3. 40 CFR 180.1130 - N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 24 2014-07-01 2014-07-01 false N-(n-octyl)-2-pyrrolidone and N-(n... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1130 N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a tolerance. (a)...

  4. 40 CFR 721.10055 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. 721.10055 Section 721.10055 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. (a) Chemical substance...

  5. 40 CFR 721.10473 - 1-Propanaminium, 3-amino-N-(2-carboxyethyl)-N,N-dimethyl-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false 1-Propanaminium, 3-amino-N-(2-carboxyethyl)-N,N-dimethyl-, N-coco acyl derivs., inner salts. 721.10473 Section 721.10473 Protection of...-amino-N-(2-carboxyethyl)-N,N-dimethyl-, N-coco acyl derivs., inner salts. (a) Chemical substance...

  6. 40 CFR 180.1130 - N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 25 2012-07-01 2012-07-01 false N-(n-octyl)-2-pyrrolidone and N-(n... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1130 N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a tolerance....

  7. 40 CFR 721.10055 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. 721.10055 Section 721.10055 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. (a) Chemical substance...

  8. 40 CFR 721.10055 - 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false 1-Propanaminium, 3-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. 721.10055 Section 721.10055 Protection of...-amino-N-(carboxymethyl)-N,N-dimethyl-, N-soya acyl derivs., inner salts. (a) Chemical substance...

  9. 40 CFR 721.10473 - 1-Propanaminium, 3-amino-N-(2-carboxyethyl)-N,N-dimethyl-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false 1-Propanaminium, 3-amino-N-(2-carboxyethyl)-N,N-dimethyl-, N-coco acyl derivs., inner salts. 721.10473 Section 721.10473 Protection of...-amino-N-(2-carboxyethyl)-N,N-dimethyl-, N-coco acyl derivs., inner salts. (a) Chemical substance...

  10. 40 CFR 180.1130 - N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 24 2011-07-01 2011-07-01 false N-(n-octyl)-2-pyrrolidone and N-(n... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1130 N-(n-octyl)-2-pyrrolidone and N-(n-dodecyl)-2-pyrrolidone; exemptions from the requirement of a tolerance....

  11. In vitro stimulation of macrophages by quadrol [N,N,N',N'-tetrakis(2-hydroxypropyl)ethylenediamine].

    PubMed

    Bhide, M V; Patel, S; Rowland, E C; Smith, D J

    1985-01-01

    Mouse peritoneal macrophages, when exposed to Quadrol [N,N,N',N'-tetrakis(2-hydroxypropyl)ethylenediamine] in vitro, show a dose dependent enhanced spreading over a four-hour period. In vitro Quadrol induced phagocytosis of polystyrene beads was found to be time and concentration dependent. The rate and extent of the enhancement of phagocytosis was comparable to that observed for lipopolysaccharide and tuftsin.

  12. Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation.

    PubMed

    Criton, Marc; Le Mellay-Hamon, Véronique

    2008-06-15

    A series of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea analogues were prepared and evaluated as inhibitors of tyrosinase and melanin formation. The most active analogue 1 inhibited mushroom tyrosinase with an IC(50) of around 0.29 microM and also retained a substantial potency in cell culture by reducing pigment synthesis by 78%. Therefore, compound 1 could be considered as a promising candidate for preclinical drug development for skin hyperpigmentation application.

  13. Distributed bragg reflector using AIGaN/GaN

    DOEpatents

    Waldrip, Karen E.; Lee, Stephen R.; Han, Jung

    2004-08-10

    A supported distributed Bragg reflector or superlattice structure formed from a substrate, a nucleation layer deposited on the substrate, and an interlayer deposited on the nucleation layer, followed by deposition of (Al,Ga,B)N layers or multiple pairs of (Al,Ga,B)N/(Al,Ga,B)N layers, where the interlayer is a material selected from AlN, Al.sub.x Ga.sub.1-x N, and AlBN with a thickness of approximately 20 to 1000 angstroms. The interlayer functions to reduce or eliminate the initial tensile growth stress, thereby reducing cracking in the structure. Multiple interlayers utilized in an AlGaN/GaN DBR structure can eliminate cracking and produce a structure with a reflectivity value greater than 0.99.

  14. N44C nebula

    NASA Technical Reports Server (NTRS)

    1999-01-01

    Resembling the hair in Botticelli's famous portrait of the birth of Venus, an image from NASA's Hubble Space Telescope has captured softly glowing filaments streaming from hot young stars in a nearby nebula.

    The image, presented by the Hubble Heritage Project, was taken in 1996 by Hubble's Wide Field and Planetary Camera 2, designed and built by NASA's Jet Propulsion Laboratory, Pasadena, Calif. The image is available online at

    http://heritage.stsci.edu , http://oposite.stsci.edu/pubinfo/pr/2002/12 orhttp://www.jpl.nasa.gov/images/wfpc .

    On the top right of the image is a source of its artistic likeness, a network of nebulous filaments surrounding the Wolf-Rayet star. This type of rare star is characterized by an exceptionally vigorous 'wind' of charged particles. The shock of the wind colliding with the surrounding gas causes the gas to glow.

    The Wolf-Rayet star is part of N44C, a nebula of glowing hydrogen gas surrounding young stars in the Large Magellanic Cloud. Visible from the Southern Hemisphere, the Large Magellanic Cloud is a small companion galaxy to the Milky Way.

    What makes N44C peculiar is the temperature of the star that illuminates it. The most massive stars -- those that are 10 to 50 times more massive than the Sun -- have maximum temperatures of 30,000 to 50,000 degrees Celsius (54,000 to 90,000 degrees Fahrenheit). The temperature of this star is about 75,000 degrees Celsius (135,000 degrees Fahrenheit). This unusually high temperature may be due to a neutron star or black hole that occasionally produces X-rays but is now inactive.

    N44C is part of a larger complex that includes young, hot, massive stars, nebulae, and a 'superbubble' blown out by multiple supernova explosions. Part of the superbubble is seen in red at the very bottom left of the Hubble image.

    The Space Telescope Science Institute is operated by the Association of Universities for Research in Astronomy, Inc., for NASA, under contract with the Goddard

  15. Ion irradiation induced disappearance of dislocations in a nickel-based alloy

    NASA Astrophysics Data System (ADS)

    Chen, H. C.; Li, D. H.; Lui, R. D.; Huang, H. F.; Li, J. J.; Lei, G. H.; Huang, Q.; Bao, L. M.; Yan, L.; Zhou, X. T.; Zhu, Z. Y.

    2016-06-01

    Under Xe ion irradiation, the microstructural evolution of a nickel based alloy, Hastelloy N (US N10003), was studied. The intrinsic dislocations are decorated with irradiation induced interstitial loops and/or clusters. Moreover, the intrinsic dislocations density reduces as the irradiation damage increases. The disappearance of the intrinsic dislocations is ascribed to the dislocations climb to the free surface by the absorption of interstitials under the ion irradiation. Moreover, the in situ annealing experiment reveals that the small interstitial loops and/or clusters induced by the ion irradiation are stable below 600 °C.

  16. Applied N=1 Supergravity

    NASA Astrophysics Data System (ADS)

    Nath, Pran

    A review of recent developments in the applications of N=1 Supergravity to the construction of unified models of elementary particle interactions is given. Couplings of N=1 Supergravity with matter consisting of an arbitrary set of l handed multiplets and a gauge multiplet are discussed. General formulation of spontaneous symmetry breaking and the criteria for breaking of internal symmetry and of local supersymmetry are described. Construction of specific Supergrvity GUT models, the gauge heirarchy in GUT models and a deduction of the low energy effective potential are discussed. The phenomena of SU(2)XU(1) electro-weak gauge invariance breakdown by Supergravity in tree models and by radiative corrections using renormalization group methods are described. Model independent formulations of low energy physics which encompass tree and the renormalization group methods of breaking SU(2)XU(1), but also allow more general scenarios are discussed. The particle content of Supergravity unified theories at low energy is given which includes predictions, for a class of supergravity models, of light gauge fermins, i.e. of a charged Dirac fermion, the Wino, with a mass below the W boson mass and a neutral fermion, the Zino, below the mass of the Z boson mass. "Direct" gaugino masses arising from loops for the photino and the gluino, (which are massless at the tree level) are exhibited. Decays of the W and Z into photino. Vino, and Zino modes and their branching ratios into various channels are given. Experimental signals for the supersymmetrie decays are discussed and some prominent signatures such as decays into one and two jets with unbalanced energy and momentum are pointed out. The current status of the ρ-parameter, including supergravity GUT effects is given. Other experimental consequences of supergravity unified theories are also discussed.

  17. Cyclo-hexyl-methyl-ammonium N,N'-dicyclo-hexyl-N,N'-dimethyl-N''-(2,2,2-trifluoro-acet-yl)phospho-nic triamide).

    PubMed

    Yazdanbakhsh, Mohammad; Eshtiagh-Hosseini, Hossein; Sabbaghi, Fahimeh

    2008-12-10

    In the salt, C(7)H(16)N(+)·C(16)H(28)F(3)N(3)O(2)P(-), the P atom shows tetra-hedral coordination. Two ion pairs are linked by N-H⋯O hydrogen bonds across a center of inversion. The phosphoryl and carbonyl groups are staggered [O-P-N-C = 64.8 (3)°].

  18. Relativistic scalar-vector models of the N-N and N-nuclear interactions

    SciTech Connect

    Green, A.E.S.

    1985-01-01

    This paper for the Proceedings of Conference an Anti-Nucleon and Nucleon-Nucleus Interactions summarizes work by the principal investigator and his collaborators on the nucleon-nucleon (N-N) and nucleon-nuclear (N-eta) interactions. It draws heavily on a paper presented at the Many Body Conference in Rome in 1972 but also includes a brief review of our phenomenological N-eta interaction studies. We first summarize our 48-49 generalized scalar-vector meson field theory model of the N-N interactions. This is followed by a brief description of our phenomenological work in the 50's on the N-eta interaction sponsored by the Atomic Energy Commission (the present DOE). This work finally led to strong velocity dependent potentials with spin orbit and isospin terms for shell and optical model applications. This is followed by a section on the Emergence of One-Boson Exchange Models describing developments in the 60's of quantitative generalized one boson exchange potentials (GOBEP) including our purely relativistic N-N analyses. Then follows a section on the application of this meson field model to the N-eta interaction, in particular to spherical closed shell nuclei. This work was sponsored by AFOSR but funding was halted with the Mansfield amendment. We conclude with a discussion of subsequent collateral work by former colleagues and by others who have converged upon scalar-vector relativistic models of N-N, antiN-N, N-eta and antiN-eta interactions and some lessons learned from this extended endeavor. 61 refs.

  19. N abundance of nodules as an indicator of N metabolism in n(2)-fixing plants.

    PubMed

    Shearer, G; Feldman, L; Bryan, B A; Skeeters, J L; Kohl, D H; Amarger, N; Mariotti, F; Mariotti, A

    1982-08-01

    This paper expands upon previous reports of (15)N elevation in nodules (compared to other tissues) of N(2)-fixing plants. N(2)-Fixing nodules of Glycine max (soybeans), Vigna unguiculata (cowpea), Phaseolus vulgaris (common bean), Phaseolus coccineus (scarlet runner bean), Prosopis glandulosa (mesquite), and Olneya tesota (desert ironwood) were enriched in (15)N. Nodules of Vicia faba (fava beans), Arachis hypogaea (peanut), Trifolium pratense (red clover), Pisum sativum (pea), Lathyrus sativus (grass pea), Medicago sativa (alfalfa), and Lupinus mutabilis (South American lupine) were not; nor were the nodules of nine species of N(2)-fixing nonlegumes. The nitrogen of ineffective nodules of soybeans and cowpeas was not enriched in (15)N. Thus, (15)N elevation in nodules of these plants depends on active N(2)-fixation. Results obtained so far on the generality of (15)N enrichment in N(2)-fixing nodules suggest that only the nodules of plants which actively fix N(2) and which transport allantoin or allantoic acid exhibit (15)N enrichment.

  20. Capture cross sections of 15N(n, γ)16N at astrophysical energies

    NASA Astrophysics Data System (ADS)

    Fan, Guang-Wei; Ma, Jun-Bing; Sheng, Zong-Qiang; Shi, Guo-Zhu; Tian, Feng; Wang, Jun; Zhang, Chao

    2016-12-01

    We have reanalyzed reaction cross sections of 16N on a 12C target. The nucleon density distribution of 16N, especially surface density distribution, was extracted using the modified Glauber model. On the basis of dilute surface densities, the 15N(n, γ)16N reaction is discussed within the framework of the direct capture reaction mechanism. The calculations agree quite well with the experimental data. Support given by National Natural Science Foundation of China (11447236, 11505002, 11247001) and Foundation of Anhui University of Science and Technology (11130, 12608)

  1. Terahertz Generation in GaN/AlGaN Superlattices

    DTIC Science & Technology

    2009-02-28

    Morkoc, hmorkoc@vcu.edu Organization: Title: Program manager: Virginia Commonwealth University Terahertz generation in GaN /AlGaN superlattices...Final 3. DATES COVERED (From - To) 08/01/07-11/30/08 4. TITLE AND SUBTITLE THZ-OSCILLATIONS IN GAN /ALUMINUM GAN SUPERLATTICES 5a. CONTRACT NUMBER...that we learned in structures grown on GaN substrates which we believe will give way to tunneling dominated current at resonant states. Once we

  2. Tertiary amine N-oxides as bioreductive drugs: DACA N-oxide, nitracrine N-oxide and AQ4N.

    PubMed Central

    Wilson, W. R.; Denny, W. A.; Pullen, S. M.; Thompson, K. M.; Li, A. E.; Patterson, L. H.; Lee, H. H.

    1996-01-01

    Tertiary amine N-oxides of DNA intercalators with alkylamino sidechains are a new class of bioreductive drugs. N-oxidation masks the cationic charge of the amines, forming prodrugs with low DNA binding affinity and low toxicity which can be activated selectively by metabolic reduction under hypoxic conditions. This study compares three intercalator N-oxides (NC-NO, DACA-NO and AQ4N), which, respectively, give nitracrine (NC), DACA and AQ4 on reduction. In aerobic cell culture all three N-oxide were much less toxic than the corresponding amines, and showed large increases in cytotoxicity under hypoxia. The topoisomerase poisons DACA and AQ4 (and their N-oxides) were less active against non-cycling than cycling cells. However, only AQ4N was active against the mouse mammary tumour MDAH-MCa-4. This dialkylaminoanthraquinone-di-N-oxide has activity at least as great as the reference bioreductive drug RB 6145 against this tumour, both with and without radiation and when combined with the tumour blood flow inhibitor 5,6-dimethylxanthenone-4-acetic acid (DMXAA). It is suggested that the high in vivo activity of AQ4N relative to the other topoisomerase-targeted N-oxide, DACA-NO, may be in part due to release in hypoxic cells of an intracalator with sufficiently high DNA binding affinity that it is retained long enough to kill non-cycling cells when they eventually re-enter the cell cycle. PMID:8763844

  3. Electrochemical fluorination of trichloroethylene and N, N-dimethyltrifluoroacetamide

    NASA Technical Reports Server (NTRS)

    Hsu, L. C.

    1979-01-01

    Fluorination of trichloroethylene and N, N-dimethyltrifluoroacetamide was carried out on a laboratory scale in an advanced Simons type electrochemical apparatus which could be operated automatically from ambient to 50 psi pressure. A variety of fluorine-substituted products are formed, depending upon electrolysis conditions and concentrations of reactant relative to the NaF, KF, HF electrolyte. A new reaction mechanism of electrochemical fluorination of trichloroethylene is proposed. The solvency-to-fluorine content relationship of fluorinated N, N-dimethyltrifluoroacetamide is described.

  4. Electrochemical fluorination of trichloroethylene and N, N-dimethyltrifluoroacetamide

    NASA Technical Reports Server (NTRS)

    Hsu, L.-C.

    1979-01-01

    The paper presents the results of experiments concerning the fluorination of trichloroethylene and N, N-dimethyltrifluoroacetamide carried out on a laboratory scale in an advanced 'Simons' type electrochemical apparatus which could be operated automatically from ambient to 50 psi pressure. It is shown that a variety of fluorine-substituted products are formed, depending upon electrolysis conditions and concentrations of reactant relative to the NaF, KF, HF electrolyte. A new reaction mechanism of electrochemical fluorination of trichloroethylene is proposed. Finally, the solvency-to-fluorine content relationship of fluorinated N, N-dimethyltrifluoroacetamide is described.

  5. Radiation hardness of n-GaN schottky diodes

    SciTech Connect

    Lebedev, A. A. Belov, S. V.; Mynbaeva, M. G.; Strel’chuk, A. M.; Bogdanova, E. V.; Makarov, Yu. N.; Usikov, A. S.; Kurin, S. Yu.; Barash, I. S.; Roenkov, A. D.; Kozlovski, V. V.

    2015-10-15

    Schottky-barrier diodes with a diameter of ∼10 µm are fabricated on n-GaN epitaxial films grown by hydride vapor-phase epitaxy (HVPE) on sapphire substrates. The changes in the parameters of the diodes under irradiation with 15 MeV protons are studied. The carrier removal rate was found to be 130–145 cm{sup –1}. The linear nature of the dependence N = f(D) (N is the carrier concentration, and D, the irradiation dose) shows that compensation of the material is associated with transitions of electrons from shallow donors to deep acceptor levels which are related to primary radiation defects.

  6. Light dilaton in the large N tricritical O (N ) model

    NASA Astrophysics Data System (ADS)

    Omid, Hamid; Semenoff, Gordon W.; Wijewardhana, L. C. R.

    2016-12-01

    The leading order of the large N limit of the O (N ) symmetric phi-six theory in three dimensions has a phase which exhibits spontaneous breaking of scale symmetry accompanied by a massless dilaton which is a Goldstone boson. At the next-to-leading order in large N , the phi-six coupling has a beta function of order 1 /N and it is expected that the dilaton acquires a small mass, proportional to the beta function and the condensate. In this article, we show that this "light dilaton" is actually a tachyon. This indicates an instability of the phase of the theory with spontaneously broken approximate scale invariance.

  7. N=1 deformations and RG flows of N=2 SCFTs

    NASA Astrophysics Data System (ADS)

    Maruyoshi, Kazunobu; Song, Jaewon

    2017-02-01

    We study certain N=1 preserving deformations of four-dimensional N=2 superconformal field theories (SCFTs) with non-abelian flavor symmetry. The deformation is described by adding an N=1 chiral multiplet transforming in the adjoint representation of the flavor symmetry with a superpotential coupling, and giving a nilpotent vacuum expectation value to the chiral multiplet which breaks the flavor symmetry. This triggers a renormalization group flow to an infrared SCFT. Remarkably, we find classes of theories flow to enhanced N=2 supersymmetric fixed points in the infrared under the deformation. They include generalized Argyres-Douglas theories and rank-one SCFTs with non-abelian flavor symmetries. Most notably, we find renormalization group flows from the deformed conformal SQCDs to the ( A 1 , A n ) Argyres-Douglas theories. From these "Lagrangian descriptions," we compute the full superconformal indices of the ( A 1 , A n ) theories and find agreements with the previous results. Furthermore, we study the cases, including the T N and R 0, N theories of class S and some of rank-one SCFTs, where the deformation gives genuine N=1 fixed points.

  8. Reverse bias leakage current mechanism of AlGaN/InGaN/GaN heterostructure

    NASA Astrophysics Data System (ADS)

    Chakraborty, Apurba; Ghosh, Saptarsi; Mukhopadhyay, Partha; Jana, Sanjay K.; Dinara, Syed Mukulika; Bag, Ankush; Mahata, Mihir K.; Kumar, Rahul; Das, Subhashis; Das, Palash; Biswas, Dhrubes

    2016-03-01

    The reverse bias leakage current mechanism of AlGaN/InGaN/GaN heterostructure is investigated by current-voltage measurement in temperature range from 298 K to 423 K. The Higher electric field across the AlGaN barrier layer of AlGaN/InGaN/GaN double heterostructure due to higher polarization charge is found to be responsible for strong Fowler-Nordheim (FN) tunnelling in the electric field higher than 3.66 MV/cm. For electric field less than 3.56 MV/cm, the reverse bias leakage current is also found to follow the trap assisted Frenkel-Poole (FP) emission in low negative bias region. Analysis of reverse FP emission yielded the barrier height of trap energy level of 0.34 eV with respect to Fermi level. [Figure not available: see fulltext.

  9. RBS Depth Profiling Analysis of (Ti, Al)N/MoN and CrN/MoN Multilayers

    NASA Astrophysics Data System (ADS)

    Han, Bin; Wang, Zesong; Devi, Neena; Kondamareddy, K. K.; Wang, Zhenguo; Li, Na; Zuo, Wenbin; Fu, Dejun; Liu, Chuansheng

    2017-03-01

    (Ti, Al)N/MoN and CrN/MoN multilayered films were synthesized on Si (100) surface by multi-cathodic arc ion plating system with various bilayer periods. The elemental composition and depth profiling of the films were investigated by Rutherford backscattering spectroscopy (RBS) using 2.42 and 1.52 MeV Li2+ ion beams and different incident angles (0°, 15°, 37°, and 53°). The microstructures of (Ti, Al)N/MoN multilayered films were evaluated by X-ray diffraction. The multilayer periods and thickness of the multilayered films were characterized by scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HR-TEM) and then compared with RBS results.

  10. New N,N,N',N'-tetradentate Pyrazoly Agents: Synthesis and Evaluation of their Antifungal and Antibacterial Activities.

    PubMed

    Abrigach, Farid; Bouchal, Btissam; Riant, Olivier; Macé, Yohan; Takfaoui, Abdelilah; Radi, Smaail; Oussaid, Abdelouahad; Bellaoui, Mohammed; Touzani, Rachid

    2016-01-01

    A new library of N,N,N',N' -tetradentate pyrazoly compounds containing a pyrazole moiety was synthesized by the condensation of (3,5-dimethyl-1H-pyrazol-1-yl)methanol 2a or (1H-pyrazol-1-yl)methanol 2b with a series of primary diamines in refluxed acetonitrile for 6h. The antifungal activity against the budding yeast Saccharomyces cerevisiae, as well as the antibacterial activity against Escherichia coli of these new tetradentate ligands were studied. We found that these tetradentate ligands act specifically as antifungal agents and lack antibacterial activity. Their biological activities depend on the nature of the structure of the compounds.

  11. Update of ENDL U(n,2n), U(n,gamma), U(n,f) Evaluations

    SciTech Connect

    Beck, B; Brown, D A; McNabb, D P

    2004-02-13

    The authors are in the re-evaluating of all the actinide cross section evaluations in LLNL's ENDL database, starting with uranium and focusing on inventory changing reactions. This article describes their first serious pass at updating the uranium cross section data, including estimates of cross section uncertainties. Furthermore, they are developing new tools to automate the re-evaluation and this article contains some preliminary results from these codes, namely the {sup 235}U(n, 2n) and {sup 238}U(n, 2n) evaluations.

  12. Optical characterization of AlN/GaN heterostructures

    NASA Astrophysics Data System (ADS)

    Ursaki, V. V.; Tiginyanu, I. M.; Zalamai, V. V.; Hubbard, S. M.; Pavlidis, D.

    2003-10-01

    AlN/GaN/sapphire heterostructures with AlN gate film thickness of 3-35 nm are characterized using photoreflectivity (PR) and photoluminescence (PL) spectroscopy. Under a critical AlN film thickness, the luminescence from the GaN channel layer near the interface proves to be excitonic. No luminescence related to the recombination of the two-dimensional electron gas (2DEG) is observed, in spite of high 2DEG parameters indicated by Hall-effect measurements. The increase of the AlN gate film thickness beyond a critical value leads to a sharp decrease in exciton resonance in PR and PL spectra as well as to the emergence of a PL band in the 3.40-3.45 eV spectral range. These findings are explained taking into account the formation of defects in the GaN channel layer as a result of strain-induced AlN film cracking. A model of electronic transitions responsible for the emission band involved is proposed.

  13. 4,4\\'-Methylene bis(N,N\\'-dimethyl)aniline

    Integrated Risk Information System (IRIS)

    4,4 ' - Methylene bis ( N , N ' - dimethyl ) aniline ; CASRN 101 - 61 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Haz

  14. Advanced heat exchanger development for molten salts

    DOE PAGES

    Sabharwall, Piyush; Clark, Denis; Glazoff, Michael; ...

    2014-12-01

    This study addresses present work concerned with advanced heat exchanger development for molten salt in nuclear and non nuclear thermal systems. The molten salt systems discussed herein use alloys, such as Hastelloy N and 242, which show corrosion resistance to molten salt at nominal operating temperatures up to 700°C. These alloys were diffusion welded, and the corresponding information is presented. Test specimens were prepared for exposing diffusion welds to molten salt environments. Hastelloy N and 242 were found to be weldable by diffusion welding, with ultimate tensile strengths about 90% of base metal values. Both diffusion welds and sheet materialmore » in Hastelloy N were corrosion tested in?58 mol% KF and 42 mol% ZrF4 at 650, 700, and 850°C for 200, 500, and 1,000 hours. Corrosion rates found were similar between welded and nonwelded materials, typically <10 mils per year. For materials of construction, nickel and alloys with dense nickel coatings are effectively inert to corrosion in fluorides, but not so in chlorides. Hence, additional testing of selected alloys for resistance to intergranular corrosion is needed, as is a determination of corrosion rate as a function of contaminant type and alloy composition with respect to chromium and carbon to better define the optimal chromium and carbon composition, independent of galvanic or differential solubility effects. Also presented is the division of the nuclear reactor and high temperature components per ASME standards, along with design requirements for a subcritical Rankine power cycle heat exchanger that has to overcome pressure difference of about 17 MPa.« less

  15. Advanced heat exchanger development for molten salts

    SciTech Connect

    Sabharwall, Piyush; Clark, Denis; Glazoff, Michael; Zheng, Guiqiu; Sridharan, Kumar; Anderson, Mark

    2014-12-01

    This study addresses present work concerned with advanced heat exchanger development for molten salt in nuclear and non nuclear thermal systems. The molten salt systems discussed herein use alloys, such as Hastelloy N and 242, which show corrosion resistance to molten salt at nominal operating temperatures up to 700°C. These alloys were diffusion welded, and the corresponding information is presented. Test specimens were prepared for exposing diffusion welds to molten salt environments. Hastelloy N and 242 were found to be weldable by diffusion welding, with ultimate tensile strengths about 90% of base metal values. Both diffusion welds and sheet material in Hastelloy N were corrosion tested in?58 mol% KF and 42 mol% ZrF4 at 650, 700, and 850°C for 200, 500, and 1,000 hours. Corrosion rates found were similar between welded and nonwelded materials, typically <10 mils per year. For materials of construction, nickel and alloys with dense nickel coatings are effectively inert to corrosion in fluorides, but not so in chlorides. Hence, additional testing of selected alloys for resistance to intergranular corrosion is needed, as is a determination of corrosion rate as a function of contaminant type and alloy composition with respect to chromium and carbon to better define the optimal chromium and carbon composition, independent of galvanic or differential solubility effects. Also presented is the division of the nuclear reactor and high temperature components per ASME standards, along with design requirements for a subcritical Rankine power cycle heat exchanger that has to overcome pressure difference of about 17 MPa.

  16. Radiative n 14N capture at astrophysical energies

    NASA Astrophysics Data System (ADS)

    Dubovichenko, S. B.

    2013-06-01

    In the potential cluster model with forbidden states and classification of orbital cluster states according to Young's schemes, the possibility is considered of describing the experimental data for the total cross sections of radiative n 14N capture at energies from 25.0 meV (25•10-3 eV) to 1.0 MeV. It is shown that on the whole it is possible to successfully explain the behavior of these cross sections outside the resonant energy region on the basis of the E1 transition from the 2S1/2 scattering wave with zero phase to the bound 2Р1/2 state of the 15N nucleus in the n14N channel.

  17. Proof without Words: (1 + 1/n)[superscript n] less than e less than (1 + 1/n)[superscript n+1

    ERIC Educational Resources Information Center

    Khattri, Sanjay Kumar

    2008-01-01

    We present a pictorial proof of the inequation (1 + 1/n)[superscript n] less than e less than (1 + 1/n)[superscript n+1]. The inequation is also confirmed through the Taylor expansion and alternating series theorem.

  18. 4-Bromo-N-(di-n-propyl-carbamothioyl)-benzamide.

    PubMed

    Binzet, Gün; Flörke, Ulrich; Külcü, Nevzat; Arslan, Hakan

    2009-02-04

    The synthesis of the title compound, C(14)H(19)BrN(2)OS, involves the reaction of 4-bromo-benzoyl chloride with potassium thio-cyanate in acetone followed by condensation of the resulting 4-bromo-benzoyl isothio-cyanate with di-n-propyl-amine. Typical thio-urea carbonyl and thio-carbonyl double bonds, as well as shortened C-N bonds, are observed in the title compound. The short C-N bond lengths in the centre of the mol-ecule reveal the effects of resonance in this part of the mol-ecule. The asymmetric unit of the title compound contains two crystallographically independent mol-ecules, A and B. There is very little difference between the bond lengths and angles of these mol-ecules. In mol-ecule B, one di-n-propyl group is twisted in a -anti-periplanar conformation with C-C-C-H = -179.1 (3)° and the other adopts a -synclinal conformation with C-C-C-H = -56.7 (4)°; in mol-ecule A the two di-n-propyl groups are twisted in + and -anti-periplanar conformations, with C-C-C-H = -179.9 (3) and 178.2 (3)°, respectively. In the crystal, the mol-ecules are linked into dimeric pairs via pairs of N-H⋯S hydrogen bonds.

  19. 40 CFR 721.8100 - Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy-ethyl) tal-lo-wa-mine oxide phos-phate. 721.8100... Substances § 721.8100 Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis...

  20. 40 CFR 721.8100 - Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy-ethyl) tal-lo-wa-mine oxide phos-phate. 721.8100... Substances § 721.8100 Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis...

  1. 40 CFR 721.8100 - Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy-ethyl) tal-lo-wa-mine oxide phos-phate. 721.8100... Substances § 721.8100 Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis...

  2. 40 CFR 721.8100 - Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy-ethyl) tal-lo-wa-mine oxide phos-phate. 721.8100... Substances § 721.8100 Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis...

  3. 40 CFR 721.8100 - Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis (hy-droxy-ethyl) tal-lo-wa-mine oxide phos-phate. 721.8100... Substances § 721.8100 Potassium N,N-bis (hydroxy-ethyl) cocoamine oxide phosphate, and potassium N,N-bis...

  4. 40 CFR 721.10175 - 1-Propanaminium, N-(3-aminopropyl)-2-hydroxy-N,N-dimethyl-3-sulfo-, N-(C12-18 and C18-unsatd...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 1-Propanaminium, N-(3-aminopropyl)-2-hydroxy-N,N-dimethyl-3-sulfo-, N-(C12-18 and C18-unsatd. acyl) derivs., inner salts. 721.10175 Section 721... 1-Propanaminium, N-(3-aminopropyl)-2-hydroxy-N,N-dimethyl-3-sulfo-, N-(C12-18 and C18-unsatd....

  5. 40 CFR 721.10175 - 1-Propanaminium, N-(3-aminopropyl)-2-hydroxy-N,N-dimethyl-3-sulfo-, N-(C12-18 and C18-unsatd...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false 1-Propanaminium, N-(3-aminopropyl)-2-hydroxy-N,N-dimethyl-3-sulfo-, N-(C12-18 and C18-unsatd. acyl) derivs., inner salts. 721.10175 Section 721... 1-Propanaminium, N-(3-aminopropyl)-2-hydroxy-N,N-dimethyl-3-sulfo-, N-(C12-18 and C18-unsatd....

  6. O( N) Random Tensor Models

    NASA Astrophysics Data System (ADS)

    Carrozza, Sylvain; Tanasa, Adrian

    2016-11-01

    We define in this paper a class of three-index tensor models, endowed with {O(N)^{⊗ 3}} invariance ( N being the size of the tensor). This allows to generate, via the usual QFT perturbative expansion, a class of Feynman tensor graphs which is strictly larger than the class of Feynman graphs of both the multi-orientable model (and hence of the colored model) and the U( N) invariant models. We first exhibit the existence of a large N expansion for such a model with general interactions. We then focus on the quartic model and we identify the leading and next-to-leading order (NLO) graphs of the large N expansion. Finally, we prove the existence of a critical regime and we compute the critical exponents, both at leading order and at NLO. This is achieved through the use of various analytic combinatorics techniques.

  7. Strain relaxation in (0001) AlN/GaN heterostructures

    NASA Astrophysics Data System (ADS)

    Bourret, Alain; Adelmann, Christoph; Daudin, Bruno; Rouvière, Jean-Luc; Feuillet, Guy; Mula, Guido

    2001-06-01

    The strain-relaxation phenomena during the early stages of plasma-assisted molecular-beam epitaxy growth of lattice-mismatched wurtzite (0001) AlN/GaN heterostructures have been studied by real-time recording of the in situ reflection high-energy electron diffraction (RHEED), ex situ transmission electron microscopy (TEM), and atomic-force microscopy. A pseudo-two-dimensional layer-by-layer growth is observed at substrate temperatures of 640-660 °C, as evidenced by RHEED and TEM. However, the variation of the in-plane lattice parameter during growth and after growth has been found to be complex. Three steps have been seen during the deposition of lattice-mismatched AlN and GaN layers: they were interpreted as the succession of the formation of flat platelets, 3-6 monolayers high (0.8-1.5 nm) and 10-20 nm in diameter, their partial coalescence, and gradual dislocation introduction. Platelet formation leads to elastic relaxation as high as 1.8%, i.e., a considerable part of the AlN/GaN lattice mismatch of 2.4%, and can be reversible. Platelets are always observed during the initial stages of growth and are almost insensitive to the metal/N ratio. In contrast, platelet coalescence and dislocation introduction are very dependent on the metal/N ratio: no coalescence occurs and the dislocation introduction rate is higher under N-rich conditions. In all cases, the misfit dislocation density, as measured by the irreversible relaxation, is initially of the order of 7×1011 cm-2 and decreases exponentially with the layer thickness. These results are interpreted in the framework of a model that emphasizes the important role of the flat platelets for dislocation nucleation.

  8. Method for homogenizing alloys susceptible to the formation of carbide stringers and alloys prepared thereby

    DOEpatents

    Braski, David N.; Leitnaker, James M.

    1980-01-01

    A novel fabrication procedure prevents or eliminates the reprecipitation of segregated metal carbides such as stringers in Ti-modified Hastelloy N and stainless steels to provide a novel alloy having carbides uniformly dispersed throughout the matrix. The fabrication procedure is applicable to other alloys prone to the formation of carbide stringers. The process comprises first annealing the alloy at a temperature above the single phase temperature for sufficient time to completely dissolve carbides and then annealing the single phase alloy for an additional time to prevent the formation of carbide stringers upon subsequent aging or thermomechanical treatment.

  9. Electrochemical Impedance Spectroscopy Of Metal Alloys

    NASA Technical Reports Server (NTRS)

    Macdowell, L. G.; Calle, L. M.

    1993-01-01

    Report describes use of electrochemical impedance spectroscopy (EIS) to investigate resistances of 19 alloys to corrosion under conditions similar to those of corrosive, chloride-laden seaside environment of Space Transportation System launch site. Alloys investigated: Hastelloy C-4, C-22, C-276, and B-2; Inconel(R) 600, 625, and 825; Inco(R) G-3; Monel 400; Zirconium 702; Stainless Steel 304L, 304LN, 316L, 317L, and 904L; 20Cb-3; 7Mo+N; ES2205; and Ferralium 255. Results suggest electrochemical impedance spectroscopy used to predict corrosion performances of metal alloys.

  10. Interaction of carbon atoms with Fe n, Fe n-, and Fe n+ clusters ( n=1-6)

    NASA Astrophysics Data System (ADS)

    Gutsev, Gennady L.; Bauschlicher, Charles W.

    2003-06-01

    The electronic and geometrical structures of the ground and exited states of Fe nC, Fe nC -, and Fe nC + ( n=1-6) are computed using density functional theory (DFT). Several exchange-correlation functionals are tested on FeC, for which a number of experimental results are available for comparison. Fe 2C and Fe 2C - have triangular high-spin ground states, while the ground state of Fe 2C + is a linear asymmetric Fe-C-Fe doublet whose spins at the iron sites are antiferromagnetically coupled. The natural bond analysis (NBO) allows us to qualitatively describe the nature of super exchange coupling in Fe 2C +. There is a competition between twofold and threefold sites in the Fe 3C species. Carbon is threefold coordinated in the Fe 4C and Fe 6C species, while it is fourfold coordinated in the Fe 5C clusters. Generally, attachment of a carbon atom reduces the number of unpaired electrons of an iron cluster. The maximum reduction of four is found for the largest cluster, Fe 6C. The C-Fe n bond energies in the neutral clusters are rather high, ranging from 5.5 (Fe 2C) to 6.5 eV (Fe 6C). These energies are not significantly affected by attachment or detachment of an electron to/from a Fe nC cluster. Surprisingly, the Fe-Fe n-1 , Fe-Fe n-1 C, and Fe-Fe nC bond energies are found to be nearly the same for given n. The results of our computations are in reasonable agreement with experimental data.

  11. H enhancement of N vacancy migration in GaN.

    SciTech Connect

    Wixom, Ryan R.; Wright, Alan Francis

    2005-06-01

    We have used density functional theory to investigate diffusion of V{sub N}{sup +} in the presence of H{sup +}. Optimal migration pathways were determined using the climbing image nudged elastic band and directed dimer methods. Our calculations indicate that the rate-limiting barrier for VN{sub N}{sup +} migration will be reduced by 0.58 eV by interplay with H{sup +}, which will enhance migration by more than an order of magnitude at typical GaN growth temperatures.

  12. Large N phase transitions in massive N = 2 gauge theories

    SciTech Connect

    Russo, J. G.

    2014-07-23

    Using exact results obtained from localization on S{sup 4}, we explore the large N limit of N = 2 super Yang-Mills theories with massive matter multiplets. In this talk we discuss two cases: N = 2* theory, describing a massive hypermultiplet in the adjoint representation, and super QCD with massive quarks. When the radius of the four-sphere is sent to infinity these theories are described by solvable matrix models, which exhibit a number of interesting phenomena including quantum phase transitions at finite 't Hooft coupling.

  13. Metal-free functionalization of N,N-dialkylanilines via temporary oxidation to N,N-dialkylaniline N-oxides and group transfer.

    PubMed

    Lewis, Robert S; Wisthoff, Michael F; Grissmerson, J; Chain, William J

    2014-07-18

    A simple set of protocols for the controlled elaboration of anilines is reported allowing access to a diverse array of aminophenols, aminoarylsulfonates, alkylated anilines, and aminoanilines in 29-95% yield in a single laboratory operation from easily isolable, bench-stable N,N-dialkylaniline N-oxides. The introduction of new C-O, C-C, and C-N bonds on the aromatic ring is made possible by a temporary increase in oxidation level and excision of a weak N-O bond.

  14. The effect of N-substituted alkyl groups on the anticonvulsant activities ofN-Cbz-alpha-amino-N-alkylsuccinimides.

    PubMed

    Lee, J; Son, K; Jung, K; Choi, J; Park, M

    1997-02-01

    For the purpose of defining the effects of theN-substituted alkyl groups on the anticonvulsant activities ofN-Cbz-alpha-aminosuccinimides, various (R)-and(S)-N-alkyl substitutedN-Cbz-alpha-aminosuccinimides (1 and2) were prepared from the corresponding (R)-and(S)-N-Cbz-aspartic acid by using known reaction and were evaluated the anticonvulsant activies in the MES and PTZ tests, including their neurotoxicities. The most active compound in the MES test was(R)-N-Cbz-alpha-amino-N-methylsuccinimide (1b) (ED(50)=52.5 mg/kg, Pl-3.2). And in case of the PTZ test,(R)-N-Cbz-alpha-amino-N-ethylsuccinimide (1c) was the most active compound (ED(50)=32.5 mg/kg, Pl=3.1). The order of anticonvulsant activities of these compounds against the MES test, as judged from the ED(50) values for theR series (1), wasN-methyl >N-isobutyl > non-substituted >N-ethyl,N-allyl >N-benzyl compound; for theS series (2)N-methyl >N-allyl > non-substituted >N-isobutyl >N-ethyl >N-benzyl compound. The anticonvulsant activities in the PTZ tests of these compounds exhibited somewhat different pattern; for theR series (1)N-ethyl >N-methyl >N-isobutyl> non-substituted >N-allyl >N-benzyl compound in order of decreasing activity; forS series (2)N-ethyl >N-allyl, non-substituted >N-isobutyl >N-methyl >N-benzyl compound in order of decreasing activity.

  15. NpN-GaN/InxGa1-xN/GaN heterojunction bipolar transistor on free-standing GaN substrate

    NASA Astrophysics Data System (ADS)

    Lochner, Zachary; Jin Kim, Hee; Lee, Yi-Che; Zhang, Yun; Choi, Suk; Shen, Shyh-Chiang; Doug Yoder, P.; Ryou, Jae-Hyun; Dupuis, Russell D.

    2011-11-01

    Data and analysis are presented for NpN-GaN/InGaN/GaN double-heterojunction bipolar transistors (HBTs) grown and fabricated on a free-standing GaN (FS-GaN) substrate in comparison to that on a sapphire substrate to investigate the effect of dislocations in III-nitride HBT epitaxial structures. The performance characteristics of HBTs on FS-GaN exhibit a maximum collector current density of ˜12.3 kA/cm2, dc current gain of ˜90, and maximum differential gain of ˜120 without surface passivation, representing a substantial improvement over similar devices grown on sapphire. This is attributed to the reduction in threading dislocation density afforded by using a homoepitaxial growth on a high-crystalline-quality substrate. The minority carrier diffusion length increases significantly owing to not only a mitigated carrier trap effect via fewer dislocations, but also possibly reduced microscopic localized states.

  16. Electron beam induced current profiling of the p-ZnO:N/n-GaN heterojunction

    SciTech Connect

    Przeździecka, E. Stachowicz, M.; Chusnutdinow, S.; Jakieła, R.; Kozanecki, A.

    2015-02-09

    The high quality p-n structures studied consist of nitrogen doped ZnO:N films grown by plasma assisted molecular beam epitaxy on n-type GaN templates. The nitrogen concentration, determined by secondary ion mass spectroscopy, is about 1 × 10{sup 20} cm{sup −3}. Temperature dependent photoluminescence studies confirm the presence of acceptor centers with an energy level lying approximately 130 meV above the valence band. The maximum forward-to-reverse current ratio I{sub F}/I{sub R} in the obtained p-n diodes is about 10{sup 7} at ±5 V, which is 2–5 orders of magnitude higher than previously reported for this type of heterojunctions. Electron-beam-induced current measurements confirm the presence of a p–n junction, located at the p-ZnO/n-GaN interface. The calculated diffusion length and activation energy of minority carriers are presented. The heterostructures exhibit strong absorption in the UV range with a four orders of magnitude high bright-to-dark current ratio.

  17. Blockade involving high- n, n ~ 300 , strontium Rydberg atoms

    NASA Astrophysics Data System (ADS)

    Yoshida, Shuhei; Burgdörfer, Joachim; Zhang, Xinyue; Dunning, F. Barry

    2016-05-01

    The blockade of high- n strontium n1F3 Rydberg states contained in a hot atomic beam is investigated both theoretically and experimentally. One difficulty in such experiments is that, once created, Rydberg atoms move out of the excitation volume reducing blockade effects. While the effects of such motion are apparent, the data provide strong evidence of blockade, consistent with theoretical predictions. Because of their relatively high angular momentum (L = 3) , a pair of n1F3 Rydberg atoms have many degenerate states whose degeneracy is removed by Rydberg-Rydberg interactions yielding a high density of states near the target energy. To evaluate the effect of blockade not only the energy shifts but also the modification of the oscillator strengths for excitation have to be taken into account. The n-scaling of the interactions and the importance of high-order multipoles will also be discussed. Research supported by the NSF and Robert A. Welch Foundation.

  18. Investigation of 110Cd with the (n ,n' γ) reaction

    NASA Astrophysics Data System (ADS)

    Garrett, P. E.; Bangay, J.; Diaz Varela, A.; Green, K. L.; Jigmeddorj, B.; Sumithrarachchi, C.; Jolie, J.; Warr, N.; Hannant, C. D.; Orce, N.; Yates, S. W.

    2013-10-01

    Excited states in 110Cd have been investigated with the (n ,n' γ) reaction using monoenergetic neutrons. Excitation functions, using neutron energies in the range of 2 MeV to 3.4 MeV were collected, and γ-ray angular distributions at neutron energies of 2.6, 2.9, and 3.4 MeV were performed. The (n ,n' γ) results were complemented with γγ coincidences from a 110In β-decay experiment (see contribution by A. Diaz Varela) performed at TRIUMF. This has resulted in a comprehensive level scheme for 110Cd below ~ 3 MeV, including stringent limits on unobserved transitions. Level lifetimes were extracted using the Doppler shift attenuation technique. Comparison of the results with simplified model expectations suggests that the low-lying structure of 110Cd is that of a deformed γ-soft rotor, rather than a spherical vibrator.

  19. AlGaN/GaN plasmonic terahertz electronic devices

    NASA Astrophysics Data System (ADS)

    Shur, Michael

    2014-03-01

    A very large electron sheet density and a relatively long momentum relaxation time of the two-dimensional electron gas in III-N heterostructures makes this materials system to be very attractive for plasmonic electronics applications.

  20. Sustainable development in an N-rich/n-poor world.

    PubMed

    Perrings, Charles; Kinzig, Ann; Halkos, George

    2014-11-01

    Sustainable development requires that per capita inclusive wealth-produced, human, and natural capital-does not decline over time. We investigate the impact of changes in nitrogen on inclusive wealth. There are two sides to the nitrogen problem. Excess use of nitrogen in some places gives rise to N-pollution, which can cause environmental damage. Insufficient replacement of nitrogen in other places gives rise to N-depletion, or loss of nutrient stocks. Neither is explicitly accounted for in current wealth measures, but both affect wealth. We calculate an index of net N-replacement, and investigate its relationship to wealth. In countries with low levels of relative N-loss, we find that the uncompensated loss of soil nitrogen in poorer countries is associated with declining rates of growth of inclusive per capita wealth. What is less intuitive is that increasing fertilizer application in both rich and poor countries can increase per capita inclusive wealth.

  1. Experimental observation of N00N state Bloch oscillations.

    PubMed

    Lebugle, Maxime; Gräfe, Markus; Heilmann, René; Perez-Leija, Armando; Nolte, Stefan; Szameit, Alexander

    2015-09-22

    Bloch oscillations of quantum particles manifest themselves as periodic spreading and relocalization of the associated wave functions when traversing lattice potentials subject to external gradient forces. Albeit this phenomenon is deeply rooted into the very foundations of quantum mechanics, all experimental observations so far have only contemplated dynamics of one and two particles initially prepared in separable local states. Evidently, a more general description of genuinely quantum Bloch oscillations will be achieved on excitation of a Bloch oscillator by nonlocal states. Here we report the observation of Bloch oscillations of two-particle N00N states, and discuss the nonlocality on the ground of Bell-like inequalities. The time evolution of two-photon N00N states in Bloch oscillators, whether symmetric, antisymmetric or partially symmetric, reveals transitions from particle antibunching to bunching. Consequently, the initial states can be tailored to produce spatial correlations akin to those of bosons, fermions and anyons, presenting potential applications in photonic quantum simulation.

  2. Graphene in ohmic contact for both n-GaN and p-GaN

    SciTech Connect

    Zhong, Haijian; Liu, Zhenghui; Shi, Lin; Xu, Gengzhao; Fan, Yingmin; Huang, Zengli; Wang, Jianfeng; Ren, Guoqiang; Xu, Ke

    2014-05-26

    The wrinkles of single layer graphene contacted with either n-GaN or p-GaN were found both forming ohmic contacts investigated by conductive atomic force microscopy. The local I–V results show that some of the graphene wrinkles act as high-conductive channels and exhibiting ohmic behaviors compared with the flat regions with Schottky characteristics. We have studied the effects of the graphene wrinkles using density-functional-theory calculations. It is found that the standing and folded wrinkles with zigzag or armchair directions have a tendency to decrease or increase the local work function, respectively, pushing the local Fermi level towards n- or p-type GaN and thus improving the transport properties. These results can benefit recent topical researches and applications for graphene as electrode material integrated in various semiconductor devices.

  3. New metabolic pathway for N,N-dimethyltryptamine

    SciTech Connect

    Hryhorczuk, L.M.; Rainey, J.M. Jr.; Frohman, C.E.; Novak, E.A.

    1986-01-01

    N,N-Dimethyltryptamine (DMT) undergoes a major structural alteration when added to whole human blood or its red blood cells in vitro. A new high-pressure liquid chromatography (HPLC) peak is present in extracts of these treated tissues. The compound responsible for this peak has been identified by ultraviolet spectrophotometry and by mass spectrometry as dimethylkynuramine (DMK). The enzyme responsible for this appears to be different from tryptophan 2,3-dioxygenase and also from indoleamine 2,3-dioxygenase.

  4. Photoionization studies of (BH3)n (n=1,2)

    NASA Astrophysics Data System (ADS)

    Ruščić, B.; Mayhew, C. A.; Berkowitz, J.

    1988-05-01

    The results of photoionization mass spectrometric studies on B2H6, and BH3 (produced by pyrolysis of B2H6) are presented. The photoion yield curves of B2H+n (n=2-6) and BH+n (n=2-3) from B2H6, as well as BH+n (n=1-3) from BH3 have been obtained. It is shown that the combination of appearance potential measurements for BH+3 (B2H6) and BH+3 (BH3) yields a poor upper limit for -ΔHdimerization, 0 K (BH3) of 52.7 kcal/mol, while the combination of BH+2 (B2H6) and BH+2 (BH3) provides a better upper limit (46.6±0.6 kcal/mol) for this quantity. However, the threshold for BH+ (BH3), combined with auxiliary data, provides the best current experimental value, (34.3-39.1)±2 kcal/mol. This experimental value is in good agreement with a recent ab initio calculation, and is arrived at by using the best current estimate of ΔHf(B2H6), rather than a radically different value proposed in that paper. The ionization potential of BH3, ΔHf (BH+2), and the atomization energy of BH3 obtained experimentally are in excellent agreement with other ab initio calculations. The upper limits on heats of formation for the ionic species B2H+n (n=2-6) are obtained, and plausible structures are discussed for these species, based on the current energetics and various ab initio calculations. Finally, the fragmentation behavior of photoions from diborane is shown to have a more facile explanation by quasiequilibrium theory than by a molecular orbital picture, with the probable exception of BH+3 (B2H6).

  5. [N,N-Bis(diphenyl-phosphino)isopropyl-amine]dibromidonickel(II).

    PubMed

    Hapke, Marko; Wöhl, Anina; Peitz, Stephan; Müller, Bernd H; Spannenberg, Anke; Rosenthal, Uwe

    2009-02-06

    The title compound, [NiBr(2)(C(27)H(27)NP(2))], was synthesized by the reaction of NiBr(2)(dme) (dme is 1,2-dimethoxy-ethane) with N,N-bis-(diphenyl-phosphino)isopropyl-amine in methanol/tetra-hydro-furan. The nickel(II) center is coordinated by two P atoms of the chelating PNP ligand, Ph(2)PN(iPr)PPh(2), and two bromide ions in a distorted square-planar geometry.

  6. Heats of NF(sub n) (n= 1-3) and NF(sub n)(+)(n = 1-3)

    NASA Technical Reports Server (NTRS)

    Ricca, Alessandra; Arnold, James (Technical Monitor)

    1998-01-01

    Accurate heats of formation are computed for NF(sub n) and NF(sub n)(+), for n = 1-3. The geometries and the vibrational frequencies are determined at the B3LYP level of theory. The energetics are determined at the CCSD(T) level of theory. Basis set limit values are obtained by extrapolation. In those cases where the CCSD(T) calculations become prohibitively large, the basis set extrapolation is performed at the MP2 level. The temperature dependence of the heat of formation, heat capacity, and entropy are computed for the temperature range 300 to 4000 K and fit to a polynomial.

  7. InGaN quantum dot formation mechanism on hexagonal GaN/InGaN/GaN pyramids.

    PubMed

    Lundskog, A; Palisaitis, J; Hsu, C W; Eriksson, M; Karlsson, K F; Hultman, L; Persson, P O Å; Forsberg, U; Holtz, P O; Janzén, E

    2012-08-03

    Growing InGaN quantum dots (QDs) at the apex of hexagonal GaN pyramids is an elegant approach to achieve a deterministic positioning of QDs. Despite similar synthesis procedures by metal organic chemical vapor deposition, the optical properties of the QDs reported in the literature vary drastically. The QDs tend to exhibit either narrow or broad emission lines in the micro-photoluminescence spectra. By coupled microstructural and optical investigations, the QDs giving rise to narrow emission lines were concluded to nucleate in association with a (0001) facet at the apex of the GaN pyramid.

  8. [Effects of irrigation mode and N application rate on cotton field fertilizer N use efficiency and N losses].

    PubMed

    Wang, Xiao-Juan; Wei, Chang-Zhou; Zhang, Jun; Dong, Peng; Wang, Juan; Zhu, Qi-Chao; Wang, Jin-Xin

    2012-10-01

    A field experiment was conducted to study the effects of different irrigation modes (drip irrigation and furrow irrigation) and different N application rates (0, 240, 360 and 480 kg N x hm(-2)) on the fertilizer N use efficiency and N losses in a cotton field in Xinjiang, Northwest China. The main N cycling pathways, such as the N uptake by cotton plant, NO3(-)-N residual in soil, NH3 volatilization, NO3(-)-N leaching, and nitrification-denitrification, were quantitatively monitored. Compared with furrow irrigation, drip irrigation increased the seed cotton yield, plant N uptake, and fertilizer N use efficiency significantly. The NO3(-)-N residual in soil was significantly greater under furrow irrigation than under drip irrigation. With the application of fertilizer N, the N loss from NH3 volatilization under drip irrigation occupied 0.06% -0.14% of applied N, and was significantly greater than that under furrow irrigation. The N loss from NO3(-)-N leaching under drip irrigation and furrow irrigation was 4.4% and 8.8% of the applied N, respectively. Compared with furrow irrigation, drip irrigation could significantly decrease the NO3(-)-N leakage rate in leakage water. The nitrification-dinetrification loss under drip irrigation and furrow irrigation was 17.9% and 16.8% of the applied N, respectively. It was suggested that NO3(-)-N leaching and nitrification-denitrification were the main N losses in the cotton fields of Xinjiang.

  9. Laboratory experiments for Titan's ionosphere : the chemistry of N2+, N+, and N2++ nitrogen ions

    NASA Astrophysics Data System (ADS)

    Thissen, R.; Alcaraz, C.; Dutuit, O.; Nicolas, C.; Soldi-Lose, H.; Zabka, J.; Franceschi, P.

    Laboratory experiments for Titan's ionosphere : the chemistry of N+ , N+ , and N2+ nitrogen ions 2 2 R. Thissen (1), C. Alcaraz (1), O. Dutuit (1), C. Nicolas (2), H. Soldi-Lose (3), J. Zabka (4), P. Franceschi (5) (1) LCP, Bât. 350, Centre Universitaire Paris-Sud, F-91405 Orsay Cedex, France, (2) Synchrotron SOLEIL, L'Orme des Merisiers, Saint-Aubin BP 48, 91192 Gif-sur-Yvette, France, (3) Institut für Chemie, Fachgruppe Organische Chemie, Technische Universität Berlin, Straße des 17. Juni 135, D-10623 Berlin, (4) J. Heyrovsky Institute of Physical Chemistry, Dolejskova 3, CZ 18223 Praha 8 - Kobylisy, Czech Republik, (5) Dept. of Physics, University of Trento, Via Sommarive 14, 38050 Povo (TN), Italy (christian.alcaraz@lcp.u-psud.fr) N2 is the major neutral componant of Titan's atmosphere, its ionisation by solar radiation and by magnetospheric electron impact is the most important production of ions in Titan's ionosphere. These primary processes not only lead to N+ molecular 2 monocations but also to N+ atomic ions and to N2+ molecular dications, which can 2 pertain some internal or translational excitation. This contribution will summarize our efforts to caracterize in gaz phase laboratory experiments the reactivity of the nitrogen ions with the most important neutral targets of the Titan's atmosphere [1-3]: • N+ + CH4 , C2 H2 , and C2 H6 2 • N+ (3 P, 1 D) + CH4 , and C2 H4 • N2+ + N2 , CH4 , and C2 H4 2 In this work, particular attention has been paid on the effect of internal and/or translational excitation of the primary nitrogen ions on the rate constant and branching ratio of these ion-molecule reactions. The results from these studies have been compared to the literature values when available and some significant differences have been found. These new values have been used as input data in 1D models of the Titan's ionosphere to show the effect on the final density profiles of the main ions [4] and to demonstrate the existence of a N2+2 dication

  10. In-situ SEM indentation studies of the deformation mechanisms in TiN, CrN and TiN/CrN.

    PubMed

    Rzepiejewska-Malyska, K; Parlinska-Wojtan, M; Wasmer, K; Hejduk, K; Michler, J

    2009-01-01

    In this study, the microstructure and the deformation mechanisms of TiN, CrN and multilayer TiN/CrN thin films on silicon substrates were investigated. Cross-sectional lamellas of nanoindents were prepared by focused ion beam milling to observe by transmission electron microscopy the microstructure of the as-deposited and deformed materials. TiN film exhibits nanocrystalline columns, whereas CrN shows large grains. The TiN/CrN multilayer presents microstructural features typical for both materials. A film hardness of 16.9GPa for CrN, 15.8GPa for TiN and 16.6GPa for TiN/CrN was found by the nanoindentation. Reduced modulus recorded for TiN and CrN reference coatings were 221.54 and 171.1GPa, respectively, and 218.6GPa for the multilayer coating. The deformation mechanisms were observed via in-situ scanning electron microscope nanoindentation. The TiN thin film showed short radial cracks, whereas CrN deformed through pile-up and densification of the material. For TiN/CrN multilayer pile-up and cracks were found. Transmission electron microscopy observations indicated that TiN deforms through grain boundary sliding and CrN via densification and material flow. The deformation mechanism observed in TiN/CrN multilayer was found to be a mixture of both modes.

  11. Magnetic field effect on photocurrent in N,N'-di(naphthalene-l-yl)-N,N'-diphenyl-benzidine (NPB)

    NASA Astrophysics Data System (ADS)

    Li, B. K.; Chen, W. J.; Lam, M. K.; Cheah, K. W.; Wang, J. N.

    2009-11-01

    We studied organic magnetoresistance (OMAR) and magneto-photocurrent (MPC) in ITO/N,N'-di(naphthalene-l-yl)-N,N'-diplienyl-benzidine (NPB)/A1 sandwich devices with NPB thicknesses of 50 nm. Without illumination, no OMAR is observable. While the MPC curves are found to have different line shapes containing a low field and a high field component, depending on excitation photon energy and applied bias. The analysis of experimental results indicate that: (i) the magnetic field effects in NPB is associated with excitonic states, and (ii) the dissociation of singlet excitons is associated to the high field component and triplet-exciton-charge interaction is to the low field component in MPC curves.

  12. Basic studies on N''-ursodeoxycholyldiethylenetriamine-N,N,N'-triacetic acid for the dissolution of calcified gallstones.

    PubMed

    Takahashi, M; Konishi, T; Maeda, Y; Fukuzawa, M; Nishida, T; Ohya, T; Katayama, K; Kakehi, N; Sakakura, H; Takagi, A; Maeda, M; Ohama, H

    1998-06-01

    A novel calcium-chelating agent, N"-ursodeoxycholyldiethylenetriamine-N,N,N'-triacetic acid (UDCA-DTTA), was synthesized to study its ability to dissolve calcified gallstones. The chelating activity of the compound was demonstrated by dissolving calcium carbonate in vitro at a high dissolution rate. In the presence of the agent, sliced human gallstone with a composition of more than 50% calcium bilirubinate was thoroughly dissolved, indicating that calcium bilirubinate was dissolved from the gallstone. The ability to dissolve calcium was comparable to that of EDTA. However, the laminar structure of the sliced gallstone did not disappear in the presence of EDTA, whereas the structure disappeared in the presence of UDCA-DTTA. All these results indicate that UDCA-DTTA is an interesting compound as a parent substance for developing a prodrug for an oral or intravenous agent to dissolve calcium-containing gallstones.

  13. Fabrication of TiN/AlN/TiN tunnel junctions

    NASA Astrophysics Data System (ADS)

    Nakayama, Takeru; Naruse, Masato; Myoren, Hiroaki; Taino, Tohru

    2016-11-01

    We have fabricated TiN/AlN/TiN tunnel junctions with an epitaxial layer. The critical temperature of TiN can be changed in the range from 0.5 to 5.0 K. Therefore, it is easy to set 5.0 K as the target critical temperature. When a Superconducting Tunnel Junction (STJ) is operated as a photon detector, it is necessary to cool it to within 0.1 K of the critical temperature in consideration of the noise of the thermally stimulated currents. Because 0.3 K was desirable, as for the manufacture of general purpose photon detectors, the critical temperature 5.0 K. TiN and AlN films were deposited by dc and rf magnetron sputtering in a load-lock sputtering system at ambient substrate temperatures. The junctions have a gap voltage of Vg = 1.1 mV, and critical current density of Jc = 0.24 A/cm2, and Rsg/Rn of 7.2, and low subgap leakage current (Isub@ 500 μV = 180 nA). We report our experiment system, the manufacture method and the junction properties in this paper.

  14. Fast neutron scattering cross sections for terbium-159 via the (n,n'gamma) and (n,n') techniques

    NASA Astrophysics Data System (ADS)

    Seo, Pil-Neyo

    2001-08-01

    Scattering cross sections for fast neutrons were measured for low-lying levels of 159Tb, a deformed odd-A nucleus. Levels from 400 keV up to 1000 keV in excitation were studied by the (n,n'γ) technique, while elastic and inelastic scattering for the lower lying excited states were studied via the (n,n') technique. For the (n,n'γ) experiment, a Ge detector was used in conjunction with the pulsed beam time-of-flight technique to observe de-excitation gamma decays. A NaI(Tl) annulus was used to suppress signals caused by Compton scattered gamma rays. Gamma-ray production cross sections were measured in the 400- to 1000-keV incident neutron energy range in 50-keV intervals at a scattering angle of 125°. Thirty six gamma-ray transitions from 16 levels of 159.Tb were observed and placed in the decay scheme. Neutron level cross sections were inferred from the differential gamma- ray production cross sections. Neutron elastic and inelastic scattering angular distributions for this nuclide were measured via the time-of-flight technique at incident neutron energies of 575 keV and 995 keV. The neutron detector consisted of a plastic scintillator mounted on a fast photomultiplier tube. Measurements were made at 11 angles from 35° to 135° in 10-degree steps for 995 keV and at 5 angles for 575 keV. Neutrons were produced in a thin lithium target using the 7Li(p,n)7Be reaction with protons generated by the University of Massachusetts Lowell Van de Graaff Accelerator. Level cross section results using the (n,n'γ) technique are compared with the those using the (n,n') technique for lower-lying levels, 241 keV(9/2+), a three-level cluster of 348 keV(5/2+), 363 keV(5/2-), and 388 keV(7/2-), and 428 keV(7/2+) states. The results are also compared with previous work and to the ENDF/B-VI, JEF-2, and JENDL-3 evaluations.

  15. N-Consecutive-Phase Encoder

    NASA Technical Reports Server (NTRS)

    Divsalar, Dariush; Lee, Ho-Kyoung; Weber, Charles

    1995-01-01

    N-consecutive-phase encoder (NCPE) is conceptual encoder for generating alphabet of N consecutive full-response continuous-phase-modulation (CPM) signals. Enables use of binary preencoder of higher rate than used with simple continuous-phase encoder (CPE). NCPE makes possible to achieve power efficiencies and bandwidth efficiencies greater than conventional trellis coders with continuous-phase frequency-shift keying (CPFSK).

  16. More on N=8 attractors

    SciTech Connect

    Ceresole, Anna; Ferrara, Sergio; Gnecchi, Alessandra; Marrani, Alessio

    2009-08-15

    We examine a few simple extremal black hole configurations of N=8, d=4 supergravity. We first elucidate the relation between the BPS Reissner-Noerdstrom black hole and the non-BPS Kaluza-Klein dyonic black hole. Their classical entropy, given by the Bekenstein-Hawking formula, can be reproduced via the attractor mechanism by suitable choices of symplectic frame. Then, we display the embedding of the axion-dilaton black hole into N=8 supergravity.

  17. Plasma chemistries for dry etching GaN, AlN, InGaN and InAlN

    SciTech Connect

    Pearton, S.J.; Vartuli, C.B.; Lee, J.W.; Donovan, S.M.; MacKenzie, J.D.; Abernathy, C.R.; Shul, R.J.; McLane, G.F.; Ren, F.

    1996-04-01

    Etch rates up to 7,000 {angstrom}/min. for GaN are obtained in Cl{sub 2}/H{sub 2}/Ar or BCl{sub 3}/Ar ECR discharges at 1--3mTorr and moderate dc biases. Typical rates with HI/H{sub 2} are about a factor of three lower under the same conditions, while CH{sub 4}/H{sub 2} produces maximum rates of only {approximately}2,000 {angstrom}/min. The role of additives such as SF{sub 6}, N{sub 2}, H{sub 2} or Ar to the basic chlorine, bromine, iodine or methane-hydrogen plasma chemistries are discussed. Their effect can be either chemical (in forming volatile products with N) or physical (in breaking bonds or enhancing desorption of the etch products). The nitrides differ from conventional III-V`s in that bond-breaking to allow formation of the etch products is a critical factor. Threshold ion energies for the onset of etching of GaN, InGaN and InAlN are {ge} 75 eV.

  18. Potential impact of atmospheric N deposition on soil N2O emission varies with different soil N regimes

    NASA Astrophysics Data System (ADS)

    Kim, Y.; Yi, M.; Koike, T.

    2011-12-01

    Future increases in nitrogen (N) deposition has the potential to change belowground nutrient dynamics, especially N cycle, and thereby can alter the soil-atmosphere exchange of nitrous oxide (N2O) which is one of the major greenhouse gases. Moreover, we considered that their effect on soil N2O emission varies with different soil N levels because N2O is a by-product of the biological nitrification process in aerobic soil environments and of the biological denitrification process in anaerobic soil environments. To understand the changes in soil N2O flux under different soil N, we carried out simulated N addition experiment in three-year-old hybrid larch F1 (F1: Larix gmelinii var. japonica × Larix kaempferi) plantation during two growing seasons 2008 - 2009. The hybrid larch F1 was developed to make up for several problems of larch species, e.g. a high susceptibility to disease or grazing damage by insects and fungi, and a large number of this seedlings are planted recently in northern Japan. Based on soil analysis, we selected two sites which have different soil N concentration, i.e. low-N and high-N concentrations. Nitrogen input was initiated at the onset of our experiment, and included four treatments with four replications: Low-N soil + Zero-N control, Low-N soil + 50 kg-N addition, High-N soil + Zero-N control and High-N soil + 50 kg-N addition. The N was added as ammonium nitrate (NH4NO3) solution distributed in four occasions during each growing season. Gas and soil samples were taken from each plot on ten occasions at a time during each growing season. Collected N2O concentrations were determined by a gas chromatograph (GC-14B; Shimadzu, Kyoto, Japan) equipped with an electron capture detector, while total-N and inorganic-N concentrations were obtained by a NC analyzer (Sumigraph NC-1000; Sumica Chemical Analysis Service Ltd., Osaka, Japan) and an auto analyzer (AACS-4; BL-TEC Inc., Osaka, Japan), respectively. Before the N addition, initial total-N in High-N

  19. Preparation and cytotoxicity of N,N,N-trimethyl chitosan/alginate beads containing gold nanoparticles.

    PubMed

    Martins, Alessandro F; Facchi, Suelen P; Monteiro, Johny P; Nocchi, Samara R; Silva, Cleiser T P; Nakamura, Celso V; Girotto, Emerson M; Rubira, Adley F; Muniz, Edvani C

    2015-01-01

    Polyelectrolyte complex beads based on N,N,N-trimethyl chitosan (TMC) and sodium alginate (ALG) were obtained. This biomaterial was characterised by FTIR, TGA/DTG, DSC and SEM analysis. The good properties of polyelectrolyte complex hydrogel beads were associated, for the first time, with gold nanoparticles (AuNPs). Through a straightforward methodology, AuNPs were encapsulated into the beads. The in vitro cytotoxicity assays on the Caco-2 colon cancer cells and healthy VERO cells showed that the beads presented good biocompatibility on both cell lines, whereas the beads loaded with gold nanoparticles (beads/AuNPs) was slightly cytotoxic on the Caco-2 and VERO cells.

  20. Recent research progress on preparation and application of N, N, N-trimethyl chitosan.

    PubMed

    Wu, Meiyan; Long, Zhu; Xiao, Huining; Dong, Cuihua

    2016-11-03

    N,N,N-trimethyl chitosan (TMC) is a quaternized chitosan derivative with excellent solubility in aqueous solutions. It has been extensively studied as an absorption enhancer, antibacterial agent and gene vector due to its ability to form complexes with anionic gels or macromoleculars. However, the research which describes the process of TMC preparation and its new applications has not been fully reviewed. In this paper, recent progress regarding different TMC preparation methods and its characterization and application in different fields is presented. Key findings are compared and summarized and some topics for further study are suggested.

  1. Enhanced sheet carrier densities in polarization controlled AlInN/AlN/GaN/InGaN field-effect transistor on Si (111)

    SciTech Connect

    Hennig, J. Dadgar, A.; Witte, H.; Bläsing, J.; Lesnik, A.; Strittmatter, A.; Krost, A.

    2015-07-15

    We report on GaN based field-effect transistor (FET) structures exhibiting sheet carrier densities of n = 2.9 10{sup 13} cm{sup −2} for high-power transistor applications. By grading the indium-content of InGaN layers grown prior to a conventional GaN/AlN/AlInN FET structure control of the channel width at the GaN/AlN interface is obtained. The composition of the InGaN layer was graded from nominally x{sub In} = 30 % to pure GaN just below the AlN/AlInN interface. Simulations reveal the impact of the additional InGaN layer on the potential well width which controls the sheet carrier density within the channel region of the devices. Benchmarking the In{sub x}Ga{sub 1−x}N/GaN/AlN/Al{sub 0.87}In{sub 0.13}N based FETs against GaN/AlN/AlInN FET reference structures we found increased maximum current densities of I{sub SD} = 1300 mA/mm (560 mA/mm). In addition, the InGaN layer helps to achieve broader transconductance profiles as well as reduced leakage currents.

  2. Study of singlet oxygen equilibrium in dioctadecyldimethylammonium chloride vesicles employing 2-(n-(N,N,N-trimethylamine)-n-alkyl)-5-alkylfuryl halides.

    PubMed

    Zanocco, Antonio L; Meléndrez, Mónica; Günther, Germán; Lemp, Else

    2007-01-01

    Steady state photolysis and time resolved near infrared luminescence detection were employed to study the reaction kinetics of singlet oxygen with three different lipid-soluble probes incorporated in large unilamellar dioctadecyldimethylammonium chloride (DODAC) vesicles. The probes: 2-(4-(N,N,N-trimethylamine)-butyl)-5-dodecylfuryl bromide (DFTA), 2-(12-(N,N,N-trimethylamine)-dodecyl)-5-hexylfuryl bromide (HFDA) and 2-(1-(N,N,N-trimethylamine)-methyl)-5-methylfuryl iodide (MFMA) are useful in studying both singlet oxygen dynamics and its equilibrium in microcompartmentalized systems because they are actinometers in lipidic microphases. These probes contain a reactive furan ring, which will be located at different depths in the bilayer of DODAC vesicles. In the limit of the approximations, the result indicates an inhomogeneous equilibrium distribution of singlet oxygen across the bilayer. The calculated mean partitioning constant of singlet oxygen equals 2.8 and 8.3 at 20 degrees C and 40 degrees C, respectively, in the order of the previously reported constants for other microorganized systems such as sodium dodecylsulfate and cetyltrimethylammonium halide micelles and water/oil microemulsions.

  3. Diffusion technique for 15N and inorganic N analysis of low-N aqueous solutions and Kjeldahl digests.

    PubMed

    Chen, Rui Rui; Dittert, Klaus

    2008-06-01

    Diffusion of ammonia is a common sample preparation method for the stable isotope analysis of inorganic nitrogen in aqueous solution. Classical diffusion methods usually require 6-12 days of diffusion and often focus on (15)N/(14)N analysis only. More recent studies have discussed whether complete N recovery was necessary for the precise analysis of stable N isotope ratios. In this paper we present a newly revised diffusion technique that allows correct and simultaneous determination of total N and (15)N at% from aqueous solutions and Kjeldahl digests, with N concentrations down to sub-0.5-mg N L(-1) levels, and it is tested under different conditions of (15)N isotope labelling. With the modification described, the diffusion time was reduced to 72 h, while the ratios of measured and expected (15)N at% were greater than 99% and the simultaneous recovery of total N was >95%. Analysis of soil microbial biomass N and its (15)N/(14)N ratio is one of the most important applications of this diffusion technique. An experiment with soil extracts spiked with (15)N-labelled yeast showed that predigestion was necessary to prevent serious N loss during Kjeldahl digestion of aqueous samples (i.e. soil extracts). The whole method of soil microbial biomass N preparation for (15)N/(14)N analysis included chloroform fumigation, predigestion, Kjeldahl digestion and diffusion. An experiment with soil spiked with (15)N-labelled yeast was carried out to evaluate the method. Results showed a highly significant correlation of recovered and added N, with the same recovery rate (0.21) of both total N and (15)N. A k(N) value of 0.25 was obtained based on the data. In conclusion, the diffusion method works for soil extracts and microbial biomass N determination and hence could be useful in many types of soil/water studies.

  4. Theoretical and experimental studies of electric field distribution in N-polar GaN/AlGaN/GaN heterostructures

    SciTech Connect

    Gladysiewicz, M. Janicki, L.; Kudrawiec, R.; Siekacz, M.; Cywinski, G.

    2015-12-28

    Electric field distribution in N-polar GaN(channel)/AlGaN/GaN(buffer) heterostructures was studied theoretically by solving Schrodinger and Poisson equations in a self-consistent manner for various boundary conditions and comparing results of these calculations with experimental data, i.e., measurements of electric field in GaN(channel) and AlGaN layers by electromodulation spectroscopy. A very good agreement between theoretical calculations and experimental data has been found for the Fermi-level located at ∼0.3 eV below the conduction band at N-polar GaN surface. With this surface boundary condition, the electric field distribution and two dimensional electron gas concentration are determined for GaN(channel)/AlGaN/GaN(buffer) heterostructures of various thicknesses of GaN(channel) and AlGaN layers.

  5. Hepatic microsomal N-oxidation and N-demethylation of N,N-dimethylaniline in red-winged blackbird compared with rat and other birds

    USGS Publications Warehouse

    Pan, H.P.; Fouts, J.R.; Devereux, T.R.

    1975-01-01

    Hepatic microsomes prepared from red-winged blackbirds and albino rats were incubated with N,N-dimethylaniline (DMA)_in complete incubation mixtures at pH 7.9 and 37?C for 10 min. Formaldehyde and N,N-dimethylaniline--oxide produced from DMA were measured. Redwings were found to have significantly lower N-demethylation activities than rats, and redwings had only marginal or no N-oxidation activities. Hepatic microsomes from redwings did not further metabolize the N-oxide. The N-oxidation and N-demethylation activities of brown-headed cowbirds, common grackles, and starlings were similar to those of redwings.

  6. Anomalous DC and RF behavior of virgin AlGaN/AlN/GaN HEMTs

    NASA Astrophysics Data System (ADS)

    Sánchez-Martín, H.; García-Pérez, Ó.; Pérez, S.; Altuntas, P.; Hoel, V.; Rennesson, S.; Cordier, Y.; González, T.; Mateos, J.; Íñiguez-de-la-Torre, I.

    2017-03-01

    The performance of gallium nitride transistors is still limited by technological problems often related to defects and traps. In this work, virgin AlGaN/AlN/GaN HEMTs exhibiting an anomalous DC behavior accompanied by frequency dispersion in the microwave range, both in the transconductance and output conductance, are analyzed. This anomalous response, which is mitigated by high-bias conditions, is attributed to the presence of traps and defects both in the volume of the GaN channel and in the source and drain contacts. A simple equivalent circuit model is proposed to replicate the dispersive response of the transistor, achieving an excellent agreement with the measured S–parameters and thus providing relevant information about its characteristic frequency.

  7. Polarization-induced Zener tunnel diodes in GaN/InGaN/GaN heterojunctions

    SciTech Connect

    Yan, Xiaodong; Li, Wenjun; Islam, S. M.; Pourang, Kasra; Fay, Patrick; Xing, Huili; Jena, Debdeep

    2015-10-19

    By the insertion of thin In{sub x}Ga{sub 1−x}N layers into Nitrogen-polar GaN p-n junctions, polarization-induced Zener tunnel junctions are studied. The reverse-bias interband Zener tunneling current is found to be weakly temperature dependent, as opposed to the strongly temperature-dependent forward bias current. This indicates tunneling as the primary reverse-bias current transport mechanism. The Indium composition in the InGaN layer is systematically varied to demonstrate the increase in the interband tunneling current. Comparing the experimentally measured tunneling currents to a model helps identify the specific challenges in potentially taking such junctions towards nitride-based polarization-induced tunneling field-effect transistors.

  8. GaN High Power Devices

    SciTech Connect

    PEARTON,S.J.; REN,F.; ZHANG,A.P.; DANG,G.; CAO,X.A.; LEE,K.P.; CHO,H.; GILA,B.P.; JOHNSON,J.W.; MONIER,C.; ABERNATHY,C.R.; HAN,JUNG; BACA,ALBERT G.; CHYI,J.-I.; LEE,C.-M.; NEE,T.-E.; CHUO,C.-C.; CHI,G.C.; CHU,S.N.G.

    2000-07-17

    A brief review is given of recent progress in fabrication of high voltage GaN and AlGaN rectifiers, GaN/AlGaN heterojunction bipolar transistors, GaN heterostructure and metal-oxide semiconductor field effect transistors. Improvements in epitaxial layer quality and in fabrication techniques have led to significant advances in device performance.

  9. Dual Infection of Novel Influenza Viruses A/H1N1 and A/H3N2 in a Cluster of Cambodian Patients

    DTIC Science & Technology

    2011-01-01

    Vomiting N N Y Y N Rhinorrhea N N N N Y Medication Amoxicillin and paracetamol Amoxicillin and paracetamol Amoxicillin and paracetamol Amoxicillin and... paracetamol N Epidemiology Recent travel Within country N N N N Animal exposure N N N N N Disposition Recovered Recovered Recovered Recovered

  10. Sturmian function approach and {bar N}N bound states

    SciTech Connect

    Yan, Y.; Tegen, R.; Gutsche, T.; Faessler, A.

    1997-09-01

    A suitable numerical approach based on Sturmian functions is employed to solve the {bar N}N bound state problem for local and nonlocal potentials. The approach accounts for both the strong short-range nuclear potential and the long-range Coulomb force and provides directly the wave function of protonium and {bar N}N deep bound states with complex eigenvalues E=E{sub R}{minus}i({Gamma}/2). The spectrum of {bar N}N bound states has two parts, the atomic states bound by several keV, and the deep bound states which are bound by several hundred MeV. The observed very small hyperfine splitting of the 1s level and the 1s and 2p decay widths are reasonably well reproduced by both the Paris and Bonn potentials (supplemented with a microscopically derived quark annihilation potential), although there are differences in magnitude and level ordering. We present further arguments for the identification of the {sup 13}PF{sub 2} deep bound state with the exotic tensor meson f{sub 2}(1520). Both investigated models can accommodate the f{sub 2}(1520) but differ greatly in the total number of levels and in their ordering. The model based on the Paris potential predicts the {sup 13}P{sub 0} level slightly below 1.1 GeV while the model based on the Bonn potential puts this state below 0.8 GeV. It remains to be seen if this state can be identified with a scalar partner of the f{sub 2}(1520). {copyright} {ital 1997} {ital The American Physical Society}

  11. New data on ({gamma}, n), ({gamma}, 2n), and ({gamma}, 3n) partial photoneutron reactions

    SciTech Connect

    Varlamov, V. V. Ishkhanov, B. S.; Orlin, V. N.; Peskov, N. N.; Stepanov, M. E.

    2013-11-15

    Systematic discrepancies between the results of various experiments devoted to determining cross sections for total and partial photoneutron reactions are analyzed by using objective criteria of reliability of data in terms of the transitional photoneutron-multiplicity function F{sub i} = {sigma}({gamma}, in)/{sigma}({gamma}, xn), whose values for i = 1, 2, 3, ... cannot exceed by definition 1.00, 0.50, 0.33, ..., respectively. It was found that the majority of experimental data on the cross sections obtained for ({gamma}, n), ({gamma}, 2n), and ({gamma}, 3n) reactions with the aid of methods of photoneutron multiplicity sorting do not meet objective criteria (in particular, F{sub 2} > 0.50 for a vast body of data). New data on the cross sections for partial reactions on {sup 181}Ta and {sup 208}Pb nuclei were obtained within a new experimental-theoretical method that was proposed for the evaluation of cross sections for partial reactions and in which the experimental neutron yield cross section {sigma}{sup expt}({gamma}, xn) = {sigma}({gamma}, n) + 2{sigma}({gamma}, 2n) + 3{sigma}({gamma}, 3n) + ..., which is free from problems associated with determining neutron multiplicities, is used simultaneously with the functions F{sub i}{sup theor} calculated within a combined model of photonuclear reactions.

  12. Low temperature properties of spin filter NbN/GdN/NbN Josephson junctions

    NASA Astrophysics Data System (ADS)

    Massarotti, D.; Caruso, R.; Pal, A.; Rotoli, G.; Longobardi, L.; Pepe, G. P.; Blamire, M. G.; Tafuri, F.

    2017-02-01

    A ferromagnetic Josephson junction (JJ) represents a special class of hybrid system where different ordered phases meet and generate novel physics. In this work we report on the transport measurements of underdamped ferromagnetic NbN/GdN/NbN JJs at low temperatures. In these junctions the ferromagnetic insulator gadolinium nitride barrier generates spin-filtering properties and a dominant second harmonic component in the current-phase relation. These features make spin filter junctions quite interesting also in terms of fundamental studies on phase dynamics and dissipation. We discuss the fingerprints of spin filter JJs, through complementary transport measurements, and their implications on the phase dynamics, through standard measurements of switching current distributions. NbN/GdN/NbN JJs, where spin filter properties can be controllably tuned along with the critical current density (Jc), turn to be a very relevant term of reference to understand phase dynamics and dissipation in an enlarged class of JJs, not necessarily falling in the standard tunnel limit characterized by low Jc values.

  13. N,N-dimethylformamide: a multipurpose building block.

    PubMed

    Ding, Shengtao; Jiao, Ning

    2012-09-10

    Often used as a common solvent for chemical reations and utilized widely in industry as a reagent, N,N-dimethylformamide (DMF) has played an important role in organic synthesis for a long time. Numerous highly useful articles and reviews discussing its utilizations have been published. With a focus on the performance of DMF as a multipurpose precursor for various units in numerous reactions, this Minireview summarizes recent developments in the employment of DMF in the fields of formylation, aminocarbonylation, amination, amidation, and cyanation, as well as its reaction with arynes.

  14. BOC(n,n) signal multipath mitigation using MEDLL technology

    NASA Astrophysics Data System (ADS)

    Su, Xuan; Zhang, Yanmei; Su, Lianqing; Guo, Haichao

    2015-11-01

    For satellite navigation and positioning receivers are susceptible to the influence of the multipath, this paper used multipath estimating delay lock loop (MEDLL) technology for BOC (n, n) multipath signal tracking. Through the analysis of multipath signal model, it is concluded that all the multipath signal can be expressed by its amplitude, phase and delay. Then in odor to get the accurate direct signal, this paper applied MEDLL algorithm to estimate the received signal. Finally, the simulation show that this algorithm can realize multipath signal track demodulation and accurate data demodulation under a low signal noise ratio environment (SNR= -20db).

  15. Photodissociation dynamics of IBr(-)(CO(2))(n), n<15.

    PubMed

    Sanford, Todd; Han, Sang-Yun; Thompson, Matthew A; Parson, Robert; Lineberger, W Carl

    2005-02-01

    We report the ionic photoproducts produced following photoexcitation of mass selected IBr(-)(CO(2))(n), n=0-14, cluster ions at 790 and 355 nm. These wavelengths provide single state excitation to two dissociative states, corresponding to the A(') (2)Pi(1/2) and B 2 (2)Sigma(1/2) (+) states of the IBr(-) chromophore. Excitation of these states in IBr(-) leads to production of I(-)+Br and Br(-)+I( *), respectively. Potential energy curves for the six lowest electronic states of IBr(-) are calculated, together with structures for IBr(-)(CO(2))(n), n=1-14. Translational energy release measurements on photodissociated IBr(-) determine the I-Br(-) bond strength to be 1.10+/-0.04 eV; related measurements characterize the A(') (2)Pi(1/2)<--X (2)Sigma(1/2) (+) absorption band. Photodissociation product distributions are measured as a function of cluster size following excitation to the A(') (2)Pi(1/2) and B 2 (2)Sigma(1/2) (+) states. The solvent is shown to drive processes such as spin-orbit relaxation, charge transfer, recombination, and vibrational relaxation on the ground electronic state. Following excitation to the A(') (2)Pi(1/2) electronic state, IBr(-)(CO(2))(n) exhibits size-dependent cage fractions remarkably similar to those observed for I(2) (-)(CO(2))(n). In contrast, excitation to the B 2 (2)Sigma(1/2) (+) state shows extensive trapping in excited states that dominates the recombination behavior for all cluster sizes we investigated. Finally, a pump-probe experiment on IBr(-)(CO(2))(8) determines the time required for recombination on the ground state following excitation to the A(') state. While the photofragmentation experiments establish 100% recombination in the ground electronic state for this and larger IBr(-) cluster ions, the time required for recombination is found to be approximately 5 ns, some three orders of magnitude longer than observed for the analogous I(2) (-) cluster ion. Comparisons are made with similar experiments carried out on I(2

  16. Photodissociation of interstellar N2

    NASA Astrophysics Data System (ADS)

    Li, X.; Heays, A. N.; Visser, R.; Ubachs, W.; Lewis, B. R.; Gibson, S. T.; van Dishoeck, E. F.

    2013-07-01

    Context. Molecular nitrogen is one of the key species in the chemistry of interstellar clouds and protoplanetary disks, but its photodissociation under interstellar conditions has never been properly studied. The partitioning of nitrogen between N and N2 controls the formation of more complex prebiotic nitrogen-containing species. Aims: The aim of this work is to gain a better understanding of the interstellar N2 photodissociation processes based on recent detailed theoretical and experimental work and to provide accurate rates for use in chemical models. Methods: We used an approach similar to that adopted for CO in which we simulated the full high-resolution line-by-line absorption + dissociation spectrum of N2 over the relevant 912-1000 Å wavelength range, by using a quantum-mechanical model which solves the coupled-channels Schrödinger equation. The simulated N2 spectra were compared with the absorption spectra of H2, H, CO, and dust to compute photodissociation rates in various radiation fields and shielding functions. The effects of the new rates in interstellar cloud models were illustrated for diffuse and translucent clouds, a dense photon dominated region and a protoplanetary disk. Results: The unattenuated photodissociation rate in the Draine (1978, ApJS, 36, 595) radiation field assuming an N2 excitation temperature of 50 K is 1.65 × 10-10 s-1, with an uncertainty of only 10%. Most of the photodissociation occurs through bands in the 957-980 Å range. The N2 rate depends slightly on the temperature through the variation of predissociation probabilities with rotational quantum number for some bands. Shielding functions are provided for a range of H2 and H column densities, with H2 being much more effective than H in reducing the N2 rate inside a cloud. Shielding by CO is not effective. The new rates are 28% lower than the previously recommended values. Nevertheless, diffuse cloud models still fail to reproduce the possible detection of interstellar N2

  17. Extent of shielding by counterions determines the bactericidal activity of N,N,N-trimethyl chitosan salts.

    PubMed

    Follmann, Heveline D M; Martins, Alessandro F; Nobre, Thatyane M; Bresolin, Joana D; Cellet, Thelma S P; Valderrama, Patrícia; Correa, Daniel S; Muniz, Edvani C; Oliveira, Osvaldo N

    2016-02-10

    In this study, we show that the bactericidal activity of quaternized chitosans (TMCs) with sulfate, acetate, and halide counterions against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) correlates with the "availability" of N-quaternized groups [-(+)N(CH3)3] in the TMCs backbones. N,N,N-trimethyl chitosan sulfate (TMCS) and N,N,N-trimethyl chitosan acetate (TMCAc) displayed the highest activities, probably due to their delocalized π system. Among TMCs with halide counterions, activity was higher for N,N,N-trimethyl chitosan chloride (TMCCl), whereas N,N,N-trimethyl chitosan iodide (TMCI) and N,N,N-trimethyl chitosan bromide (TMCBr) exhibited lower, similar values to each other. This is consistent with the shielding of -(+)N(CH3)3 groups inferred from chemical shifts for halide counterions in (1)HNMR spectra. We also demonstrate that TMCs with distinct bactericidal activities can be classified according to their vibrational spectra using principal component analysis. Taken together, these physicochemical characterization approaches represent a predictive tool for the bactericidal activity of chitosan derivatives.

  18. Role of nanoscale AlN and InN for the microwave characteristics of AlGaN/(Al,In)N/GaN-based HEMT

    SciTech Connect

    Lenka, T. R. Panda, A. K.

    2011-09-15

    A new AlGaN/GaN-based high electron mobility transistor (HEMT) is proposed and its micro-wave characteristics are discussed by introducing a nanoscale AlN or InN layer to study the potential improvement in their high frequency performance. The 2DEG transport mechanism including various sub-band calculations for both (Al,In) N-based HEMTs are also discussed in the paper. Apart from direct current characteristics of the proposed HEMT, various microwave parameters such as transconductance, unit current gain (h{sub 21} = 1) cut-off frequency (f{sub t}), high power-gain frequency (f{sub max}). Masons available/stable gain and masons unilateral gain are also discussed for both devices to understand its suitable deployment in microwave frequency range.

  19. nEDM at SNS

    SciTech Connect

    Clayton, Steven

    2014-07-30

    This PowerPoint presentation covered the following topics: Overview; participants in the collaboration; the experimental method and Free Precession Method descriptions; and then experimental design elements, ending with a summary. A new nEDM experiment is under development with a goal sensitivity 90% CL σd < (3-5) x 10-28 e-cm in 300 live-days; Free precession method: SQUIDS to read out the 3He precession frequency, Scintillation signal for the n relative precession frequency; Dressed spin method: Strong RF field to match n and 3He effective magnetic moments; Modulation/feedback of dressing parameter based on scintillation signal; and, Ongoing development/demonstration of many aspects of the apparatus (a subset was shown here).

  20. N-(Diphenylselenio)diphenylsulfimidium tetraphenylborate.

    PubMed

    Aucott, Stephen M; Dale, Sophie H; Elsegood, Mark R J; Gilby, Liam M; Holmes, Kathryn E; Kelly, Paul F

    2005-02-01

    The title compound, C24H20NSSe+.C24H20B-, exhibits disorder (S/Se scrambling) of the chalcogen sites within the S-N-Se triad. Similar disorder was observed in the bromide salt [Aucott, Bailey, Elsegood, Gilby, Holmes, Kelly, Papageorgiou & Pedron-Haba (2004). New J. Chem. pp. 959-966]. The S-N and Se-N bond lengths are 1.6735 (15) and 1.8045 (14) A, respectively. Whereas the chalcogens in the bromide salt are involved in S...Br and Se...Br interactions of very similar distances, the scrambled S and Se sites in the title compound are involved in distinct non-bonded interactions. The site predominantly occupied by sulfur is involved in C-H...S/Se interactions, while the site predominantly occupied by selenium is involved in Se/S...pi interactions.

  1. Experimental observation of N00N state Bloch oscillations

    PubMed Central

    Lebugle, Maxime; Gräfe, Markus; Heilmann, René; Perez-Leija, Armando; Nolte, Stefan; Szameit, Alexander

    2015-01-01

    Bloch oscillations of quantum particles manifest themselves as periodic spreading and relocalization of the associated wave functions when traversing lattice potentials subject to external gradient forces. Albeit this phenomenon is deeply rooted into the very foundations of quantum mechanics, all experimental observations so far have only contemplated dynamics of one and two particles initially prepared in separable local states. Evidently, a more general description of genuinely quantum Bloch oscillations will be achieved on excitation of a Bloch oscillator by nonlocal states. Here we report the observation of Bloch oscillations of two-particle N00N states, and discuss the nonlocality on the ground of Bell-like inequalities. The time evolution of two-photon N00N states in Bloch oscillators, whether symmetric, antisymmetric or partially symmetric, reveals transitions from particle antibunching to bunching. Consequently, the initial states can be tailored to produce spatial correlations akin to those of bosons, fermions and anyons, presenting potential applications in photonic quantum simulation. PMID:26391683

  2. High-n immersion lithography

    NASA Astrophysics Data System (ADS)

    Sewell, Harry; Mulkens, Jan; Graeupner, Paul; McCafferty, Diane; Markoya, Louis; Donders, Sjoerd; Cortie, Rogier; Meijers, Ralph; Evangelista, Fabrizio; Samarakone, Nandarisi

    2008-03-01

    A two-year study on the feasibility of High-n Immersion Lithography shows very promising results. This paper reports the findings of the study. The evaluation shows the tremendous progress made in the development of second-generation immersion fluid technology. Candidate fluids from several suppliers have been evaluated. All the commercial fluids evaluated are viable, so there are a number of options. Life tests have been conducted on bench top fluid-handling systems and the results referenced to full-scale systems. Parameters such as Dose per Laser Pulse, Pulse Rate, Fluid Flow Rate, and Fluid Absorbency at 193nm, and Oxygen/Air Contamination Levels were explored. A detailed evaluation of phenomena such as Last Lens Element (LLE) contamination has been conducted. Lens cleaning has been evaluated. A comparison of High-n fluid-based technology and water-based immersion technology shows interesting advantages of High-n fluid in the areas of Defect and Resist Interaction. Droplet Drying tests, Resist Staining evaluations, and Resist Contrast impact studies have all been run. Defect-generating mechanisms have been identified and are being eliminated. The lower evaporation rate of the High-n fluids compared with water shows the advantages of High-n Immersion. The core issue for the technology, the availability of High-n optical material for use as the final lens element, is updated. Samples of LuAG material have been received from development partners and have been evaluated. The latest status of optical materials and the technology timelines are reported. The potential impact of the availability of the technology is discussed. Synergy with technologies such as Double Patterning is discussed. The prospects for <22nm (hp) are evaluated.

  3. Influence of Initial Organic N Reserves and Residual Leaf Area on Growth, N Uptake, N Partitioning and N Storage in Alfalfa (Medicago sativa) during Post-cutting Regrowth

    PubMed Central

    MEURIOT, F.; AVICE, J.-C.; SIMON, J.-C.; LAINE, P.; DECAU, M.-L.; OURRY, A.

    2004-01-01

    • Background and Aims The influence of initial residual leaf area and initial N reserves on N uptake, final N distribution, and yield in alfalfa regrowing after cutting, were studied. • Methods The effects of two levels of initial residual leaf area (plants cut to 15 cm, with (L+) or without (L−) their leaves) and two initial levels of N status [high N (HN) or low N (LN)] on growth, N uptake and N partitioning, allocation and storage after 29 d of post-cutting regrowth were analysed. • Key Results During most of the regrowth period (8–29 d after the initial harvest), HN and L+ plants had higher net N uptake rates than LN and L− plants, respectively, resulting in a greater final mineral N uptake for these treatments. However, the final partitioning of exogenous N to the regrowing shoots was the same for all treatments (67 % of total exogenous N on average). Final shoot growth, total plant N content, and N allocation to the different taproot N pools were significantly lower in plants with reduced initial leaf area and initial N reserve status. • Conclusions Although both initial residual leaf area and initial N reserves influenced alfalfa regrowth, the residual leaf area had a greater effect on final forage production and N composition in the taproot, whereas the N uptake rate and final total N content in plant were more affected by the initial N reserve status than by the residual leaf area. Moreover, N storage as proteins (especially as vegetative storage proteins, rather than nitrate or amino acids) in the taproot allowed nitrate uptake to occur at significant rates. This suggests that protein storage is not only a means of sequestering N in a tissue for further mobilization, utilization for growth or tissue maintenance, but may also indirectly influence both N acquisition and reduction capacities. PMID:15271775

  4. N-Terminal Methionine Processing.

    PubMed

    Wingfield, Paul T

    2017-04-03

    Protein synthesis is initiated by methionine in eukaryotes and by formylmethionine in prokaryotes. N-terminal methionine can be co-translationally cleaved by the enzyme methionine aminopeptidase (MAP). When recombinant proteins are expressed in bacterial and mammalian expression systems, there is a simple universal rule that predicts whether the initiating methionine will be processed by MAP based on the size of the residue adjacent (penultimate) to the N-methionine. In general, if the side chains of the penultimate residues have a radius of gyration of 1.29 Å or less, methionine is cleaved. © 2017 by John Wiley & Sons, Inc.

  5. Interface states at the SiN/AlGaN interface on GaN heterojunctions for Ga and N-polar material

    NASA Astrophysics Data System (ADS)

    Yeluri, Ramya; Swenson, Brian L.; Mishra, Umesh K.

    2012-02-01

    Dielectric passivation is important to improve the stability and reliability of gallium nitride based semiconductor devices. We need to characterize various dielectrics and their interfaces to nitrides accurately to be able to exploit the benefits efficiently. Earlier, B. L. Swenson and U. K. Mishra [J. Appl. Phys. 106, 064902 (2009)] have detailed a photo-assisted high frequency CV characterization technique for the Ga-polar SiN/GaN interface that gives an accurate value of interface state density (Dit) across the bandgap of the dielectric. In this work, we extend the technique to study the interface states at the SiN/AlGaN interface on GaN for Ga and N polar material. This simulates the AlGaN/GaN HEMT structure. A MIS-type structure comprised of a metal on SiN on an AlGaN/GaN heterojunction was used for the study. For a structure with 1 nm AlGaN interlayer, a peak interface state density of 2.8 × 1012 cm-2 eV-1 was measured. For Ga polar devices, the measured Dit decreases with increasing AlGaN thickness. In the N-polar case, the measured Dit increases with increasing AlGaN thickness. The variations of measured Dit with AlGaN thickness, in both cases, can be explained by screening from the accumulation charge at the AlGaN/GaN interface.

  6. Influence of N2 partial pressure on structural and microhardness properties of TiN/ZrN multilayers deposited by Ar/N2 vacuum arc discharge

    NASA Astrophysics Data System (ADS)

    Naddaf, M.; Abdallah, B.; Ahmad, M.; A-Kharroub, M.

    2016-08-01

    The influence of N2 partial pressure on structural, mechanical and wetting properties of multilayered TiN/ZrN thin films deposited on silicon substrates by vacuum arc discharge of (N2 + Ar) gas mixtures is investigated. X-ray diffraction (XRD) results show that the average texturing coefficient of (1 1 1) orientation and the grain size of both TiN and ZrN individual layers increase with increasing the N2 partial pressure. The Rutherford back scattering (RBS) measurements and analysis reveal that incorporation of the nitrogen in the film increases with increasing the N2 partial pressure and both TiN and ZrN individual layers have a nitrogen over-stoichiometry for N2 partial pressure ⩾50%. The change in the film micro-hardness is correlated to the changes in crystallographic texture, grain size, stoichiometry and the residual stress in the film as a function of the N2 partial pressure. In particular, stoichiometry of ZrN and TiN individual is found to play the vital role in determining the multilayer hardness. The multilayer film deposited at N2 partial pressure of 25% has the best stoichiometric ratio of both TiN and ZrN layers and the highest micro-hardness of about 32 GPa. In addition, water contact angle (WCA) measurements and analysis show a decrease in the work of adhesion on increasing the N2 partial pressure.

  7. Crystal structure of 2-carboxy- N,N,N- trimethylethanaminium bromide monohydrate

    NASA Astrophysics Data System (ADS)

    Chen, Xiao-Ming; Mak, Thomas C. W.

    1991-05-01

    A new betaine derivative, 2-carboxy- N,N,N-trimethylethanaminium bromide monohydrate, (Me 3NCH 2CH 2COOH)Br·H 2O, I, has been synthesized and characterized by X-ray crystallography. Compound I crystallizes in space group Pnma (no. 62), with a=10.452(2), b=6.855(2), c=13.737(2)Å, and Z=4. The structure ( RF=0.047 for 881 observed (⋎ FO⋎&>;6⋎ FO⋎) Mo Kα data) features a hydrogen-bonded (BR -·H 2O) ∞zigzag chain running parallel to the a axis. The quaternary ammonium ions, each attaining Cs molecular symmetry, are laterally attached by donor hydrogen bonds to the exposed water molecules of the zigzag chain. The crystal structure consists of layers each having a zipper-like arrangement of the quaternary ammonium "side-chains".

  8. catena-Poly[[(N,N-di-methyl-cyanamide-κN)lithium]-μ3-bromido].

    PubMed

    Xie, Qianwen; Tong, Hongbo; Zhou, Meisu

    2014-02-01

    The title complex, [LiBr(C3H6N2)] n , is the unexpected product of a reaction beteween (Dipp)N(Li)SiMe3 (Dipp = 2,6-diiso-propyl-phen-yl), Me2NCN and CuBr. The compound is a one-dimensional polymer with a step structure derived from the association of inversion dimers, formed by bromido ligands bridging two Li(+) cations, each of which carries a di-methyl-cyanamide ligand. The planar (LiBr)2 unit of the polymer core has a regular rhombic shape [Li-Br-Li 77.55 (16)° and Br-Li-Br 102.45 (16)°]. These (LiBr·NCNMe2)2 dimers represent the repeat unit of a polymer system propagated by additional Br-Li and Li-Br bonds generating an infinite step structure along the a-axis direction.

  9. Early changes of dog esophageal mucosa induced by N-ethyl-N'-nitro-N-nitrosoguanidine.

    PubMed

    Takubo, K; Shisa, H; Futatsuki, K; Sasajima, K

    1981-12-01

    Early changes in the esophageal mucosa of dogs induced by N-ethyl-N'-nitro-N-nitrosoguanidine (ENNG) were studied. Seven one-year-old beagle dogs were given a solution of 250 micrograms ENNG/ml to drink ad libitum for 4 months. Three different kinds of lesions (10 erosive carcinomas, 4 slightly elevated microcarcinomas and 19 leukoplakias) were recognized. These three kinds of lesions were not located adjacent to one another, and were surrounded by almost normal stratified squamous epithelium. The foci of the carcinomas revealed an abrupt transition to normal epithelium and were considered to have arisen abruptly from normal esophageal epithelium. The histogenesis of squamous cell carcinomas of the esophagus in dogs may differ from that in man.

  10. Biomaterials based on N,N,N-trimethyl chitosan fibers in wound dressing applications.

    PubMed

    Zhou, Zhongzheng; Yan, Dong; Cheng, Xiaojie; Kong, Ming; Liu, Ya; Feng, Chao; Chen, Xiguang

    2016-08-01

    In the present work, N,N,N-trimethyl chitosan (TMC) fibers were synthesized successfully and the resulting quaternized materials were characterized by FTIR. The designed TMC fibers with different degree of quaternization achieved high water absorption capability. In antibacterial activity study, TMC fibers showed high antibacterial activity than chitosan fibers against the gram-negative bacteria Escherichia coli (>63%) and gram-positive bacteria Staphylococcus aureus (>99%). TMC fibers exhibited no obvious cytotoxicity to mouse embryo fibroblast cells with low extraction concentrations (<0.05g/mL). In animal wound healing test, TMC2 fibers could significantly enhance wound re-epithelialization and contraction compared with the control (chitosan fibers). In conclusion, TMC fibers have a potential to be used as wound dressing materials.

  11. 40 CFR 721.10159 - 1-Docosanamine, N,N-dimethyl-.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 1-Docosanamine, N,N-dimethyl-. 721... Substances § 721.10159 1-Docosanamine, N,N-dimethyl-. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-docosanamine, N,N-dimethyl- (PMN...

  12. 40 CFR 721.4090 - Ethanaminium, N-[bis(diethylamino)-methylene]-N-ethyl-, bromide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Ethanaminium, N- -N-ethyl-, bromide... Substances § 721.4090 Ethanaminium, N- -N-ethyl-, bromide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as ethanaminium, N- -N-ethyl-, bromide (PMN...

  13. 40 CFR 721.275 - Halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Halogenated-N-(2-propenyl)-N... New Uses for Specific Chemical Substances § 721.275 Halogenated-N-(2-propenyl)-N-(substituted phenyl... identified generically as halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide (P-83-1085) is...

  14. 40 CFR 721.275 - Halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Halogenated-N-(2-propenyl)-N... New Uses for Specific Chemical Substances § 721.275 Halogenated-N-(2-propenyl)-N-(substituted phenyl... identified generically as halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide (P-83-1085) is...

  15. 40 CFR 721.275 - Halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Halogenated-N-(2-propenyl)-N... New Uses for Specific Chemical Substances § 721.275 Halogenated-N-(2-propenyl)-N-(substituted phenyl... identified generically as halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide (P-83-1085) is...

  16. 40 CFR 721.10159 - 1-Docosanamine, N,N-dimethyl-.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false 1-Docosanamine, N,N-dimethyl-. 721... Substances § 721.10159 1-Docosanamine, N,N-dimethyl-. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-docosanamine, N,N-dimethyl- (PMN...

  17. 40 CFR 721.4090 - Ethanaminium, N-[bis(diethylamino)-methylene]-N-ethyl-, bromide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Ethanaminium, N- -N-ethyl-, bromide... Substances § 721.4090 Ethanaminium, N- -N-ethyl-, bromide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as ethanaminium, N- -N-ethyl-, bromide (PMN...

  18. 40 CFR 721.10159 - 1-Docosanamine, N,N-dimethyl-.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false 1-Docosanamine, N,N-dimethyl-. 721... Substances § 721.10159 1-Docosanamine, N,N-dimethyl-. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-docosanamine, N,N-dimethyl- (PMN...

  19. 40 CFR 721.10576 - Polyalkenyl, N,N'-bistriazole (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Polyalkenyl, N,N'-bistriazole (generic... Specific Chemical Substances § 721.10576 Polyalkenyl, N,N'-bistriazole (generic). (a) Chemical substance... polyalkenyl, N,N'-bistriazole (PMN P-09-486) is subject to reporting under this section for the...

  20. 40 CFR 721.10159 - 1-Docosanamine, N,N-dimethyl-.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false 1-Docosanamine, N,N-dimethyl-. 721... Substances § 721.10159 1-Docosanamine, N,N-dimethyl-. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-docosanamine, N,N-dimethyl- (PMN...

  1. 40 CFR 721.4090 - Ethanaminium, N-[bis(diethylamino)-methylene]-N-ethyl-, bromide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Ethanaminium, N- -N-ethyl-, bromide... Substances § 721.4090 Ethanaminium, N- -N-ethyl-, bromide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as ethanaminium, N- -N-ethyl-, bromide (PMN...

  2. 40 CFR 721.10576 - Polyalkenyl, N,N'-bistriazole (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Polyalkenyl, N,N'-bistriazole (generic... Specific Chemical Substances § 721.10576 Polyalkenyl, N,N'-bistriazole (generic). (a) Chemical substance... polyalkenyl, N,N'-bistriazole (PMN P-09-486) is subject to reporting under this section for the...

  3. 40 CFR 721.4090 - Ethanaminium, N-[bis(diethylamino)-methylene]-N-ethyl-, bromide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Ethanaminium, N- -N-ethyl-, bromide... Substances § 721.4090 Ethanaminium, N- -N-ethyl-, bromide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as ethanaminium, N- -N-ethyl-, bromide (PMN...

  4. 40 CFR 721.275 - Halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Halogenated-N-(2-propenyl)-N... New Uses for Specific Chemical Substances § 721.275 Halogenated-N-(2-propenyl)-N-(substituted phenyl... identified generically as halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide (P-83-1085) is...

  5. 40 CFR 721.4090 - Ethanaminium, N-[bis(diethylamino)-methylene]-N-ethyl-, bromide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Ethanaminium, N- -N-ethyl-, bromide... Substances § 721.4090 Ethanaminium, N- -N-ethyl-, bromide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as ethanaminium, N- -N-ethyl-, bromide (PMN...

  6. 40 CFR 721.275 - Halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Halogenated-N-(2-propenyl)-N... New Uses for Specific Chemical Substances § 721.275 Halogenated-N-(2-propenyl)-N-(substituted phenyl... identified generically as halogenated-N-(2-propenyl)-N-(substituted phenyl) acetamide (P-83-1085) is...

  7. 40 CFR 721.10159 - 1-Docosanamine, N,N-dimethyl-.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false 1-Docosanamine, N,N-dimethyl-. 721... Substances § 721.10159 1-Docosanamine, N,N-dimethyl-. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 1-docosanamine, N,N-dimethyl- (PMN...

  8. Polarographic investigation of Cu(II) complexes with N,N,N',N'-tetrakis-(2-hydroxypropyl)-ethylenediamine.

    PubMed

    Norkus, E; Vaskelis, A; Zakaité, I; Reklaitis, J

    1995-11-01

    During investigation of the formation of Cu(2+) ion complexes with N,N,N',N'-tetrakis-(2-hydroxypropyl)-ethylenediamine (Quadrol-Q) by means of constant current polarography (20 degrees C, ionic strength J = 3 mol l(-1)), the possibility of the formation of two complex compounds; CuQ(2+) and CuQ(2+)(2), was shown within the pH range from 6 to 8. The logarithms of the stability constants for these compounds are 10.6 +/- 0.5 and 14.6 +/- 0.4 respectively. Cu(II) complexation increases sharply when the pH increases from 8 to 10. It was shown that the data at a pH of greater than 10 are in accordance with the existence of the hydroxy complexes CuQ(OH)(2) and CuQ(2)(OH)(2), the logarithms of the stability constants being 26.9 +/- 0.5 and 29.1 +/- 0.3.

  9. 40 CFR 721.7270 - 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl derivs., chloride.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-trimethyl-N-soya acyl derivs., chloride. 721.7270 Section 721.7270 Protection of Environment ENVIRONMENTAL...-soya acyl derivs., chloride. (a) Chemical substance and significant new uses subject to reporting. (1...., chloride (PMN P-01-646; CAS No. 391232-99-8) is subject to reporting under this section for the...

  10. 40 CFR 721.7270 - 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl derivs., chloride.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-trimethyl-N-soya acyl derivs., chloride. 721.7270 Section 721.7270 Protection of Environment ENVIRONMENTAL...-soya acyl derivs., chloride. (a) Chemical substance and significant new uses subject to reporting. (1...., chloride (PMN P-01-646; CAS No. 391232-99-8) is subject to reporting under this section for the...

  11. 40 CFR 721.7270 - 1-propanaminium, 3-amino-, N,N,N-trimethyl-N-soya acyl derivs., chloride.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-trimethyl-N-soya acyl derivs., chloride. 721.7270 Section 721.7270 Protection of Environment ENVIRONMENTAL...-soya acyl derivs., chloride. (a) Chemical substance and significant new uses subject to reporting. (1...., chloride (PMN P-01-646; CAS No. 391232-99-8) is subject to reporting under this section for the...

  12. Modeling of the N Cycle

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Simulation models provide a summary of the quantitative understanding of the system being modeled. The objective of this book chapter is to review the wealth of literature and the documented simulation models currently available that deal with the nitrogen (N) cycle. The fast increase in computer p...

  13. N2O FIELD STUDY

    EPA Science Inventory

    The report gives results of measurements of nitrous oxide (N2O) emissions from coal-fired utility boilers at three electric power generating stations. Six units were tested, two at each site, including sizes ranging from 165 to 700 MW. Several manufacturers and boiler firing type...

  14. N2O and NOy

    NASA Technical Reports Server (NTRS)

    Kawa, S. R.; Jackman, C. H.; Douglass, A. R.; Strahan, S. E.

    2003-01-01

    The principal loss processes for ozone in the stratosphere are either directly or indirectly closely coupled to the abundance and distribution of reactive oxides of nitrogen (NOy). The main source of NOy in the stratosphere is N2O, a trace gas that is changing significantly as a result of anthropogenic forcing. Thus diagnosis of the distributions of N2O, NOy, and their coupling is required to evaluate any chemistry-climate model aspiring to accurately simulate ozone change. In the NASA Assessment of the Effects of High-speed Aircraft in the Stratosphere: 1998 we found that the sensitivity of various models ozone to perturbation did correspond consistently with their background NOy distribution. Coordinated NOy and N2O mixing ratio distributions are available from observations: ER-2 aircraft in the lower stratosphere and ATMOS and balloon profiles to higher altitudes at a subset of latitudes and seasons. Although close comparison to these diagnostics is crucial, unfortunately the distributions are due to a combination of transport and chemical processes, and isolating the source of differences is not always simple. However, in combination with other transport and photochemical diagnostics, comparison with N2O and NOy can be very instructive in evaluation of model processes and performance.

  15. Cover crops and N credits

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Cover crops often provide many short- and long-term benefits to cropping systems. Legume cover crops can significantly reduce the N fertilizer requirement of non-legume cash crops that follow. The objectives of this presentation were to: I) educate stakeholders about the potential benefits of cover ...

  16. Concise synthesis of N,N-dimethyltryptamine and 5-methoxy-N,N-dimethyltryptamine starting with bufotenine from Brazilian Anadenanthera ssp..

    PubMed

    Moreira, Leandro A; Murta, Maria M; Gatto, Claudia C; Fagg, Christopher W; dos Santos, Maria L

    2015-04-01

    Bufotenine (1, 5-hydroxy-N,N-dimethyltryptamine) was isolated from seeds of Anadenanthera spp., a tree widespread in the Brazilian cerrado, using an efficient acid-base shakeout protocol. The conversion of bufotenine into N,N-dimethyltryptamine (4) and 5-methoxy-N,N-dimethyltryptamine (5) was accomplished through an innovative and short approach featuring the use of novel bufotenine-aminoborane complex (7). Furthermore, an easy methodology for conversion of bufotenine into 5-hydroxy-N,N,N-trimethyltryptamine (6) was well-established. This is the first study that highlights bufotenine as a resource for the production of N,N-dimethyltryptamines for either pharmacological and toxicological investigations or for synthetic purposes.

  17. [Effect of reduced N application on soil N residue and N loss in maize-soybean relay strip intercropping system].

    PubMed

    Liu, Xiao-Ming; Yong, Tai-Wen; Liu, Wen-Yu; Su, Ben-Ying; Song, Chun; Yang, Feng; Wang, Xiao-Chun; Yang, Wen-Yu

    2014-08-01

    A field experiment was conducted in 2012, including three planting pattern (maize-soybean relay strip intercropping, mono-cultured maize and soybean) and three nitrogen application level [0 kg N x hm(-2), 180 kg N x hm(-2) (reduced N) and 240 kg N x hm(-2) (normal N)]. Fields were assigned to different treatments in a randomized block design with three replicates. The objective of this work was to analyze the effects of planting patterns and nitrogen application rates on plant N uptake, soil N residue and N loss. After fertilization applications, NH4(+)-N and NO3(-)-N levels increased in the soil of intercropped maize but decreased in the soil of intercropped soybean. Compared with mono-crops, the soil N residue and loss of intercropped soybean were reduced, while those of intercropped maize were increased and decreased, respectively. With the reduced rate of N application, N residue rate, N loss rate and ammonia volatilization loss rate of the maize-soybean intercropping relay strip system were decreased by 17.7%, 21.5% and 0.4% compared to mono-cultured maize, but increased by 2.0%, 19.8% and 0.1% compared to mono-cultured soybean, respectively. Likewise, the reduced N application resulted in reductions in N residue, N loss, and the N loss via ammonia volatilization in the maize-soybean relay strip intercropping system compared with the conventional rate of N application adopted by local farmers, and the N residue rate, N loss rate and ammonia volatilization loss rate reduced by 12.0%, 15.4% and 1.2%, respectively.

  18. Descriptions of Kashmira dimorphicauda gen. n., sp. n. and Aphelenchoides hypotris sp. n. from Kashmir Valley, India

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Kashmira dimorphicauda gen. n., sp. n. and Aphelenchoides hypotris sp. n. are described and illustrated from freshwater stream soil in Kashmir Valley, India. Kashmira gen. n. is characterized by having dimorphic tails: coinoid-spicate tail in female and subcylindroid with rounded, non-spicate tip wi...

  19. Influence of internal electric fields on band gaps in short period GaN/GaAlN and InGaN/GaN polar superlattices

    SciTech Connect

    Gorczyca, I. Skrobas, K.; Suski, T.; Christensen, N. E.; Svane, A.

    2015-08-21

    The electronic structures of short period mGaN/nGa{sub y}Al{sub 1−y}N and mIn{sub y}Ga{sub 1-y}N/nGaN superlattices grown along the wurtzite c axis have been calculated for different alloy compositions y and various small numbers m of well- and n of barrier-monolayers. The general trends in gap behavior can, to a large extent, be related to the strength of the internal electric field, E, in the GaN and InGaN quantum wells. In the GaN/GaAlN superlattices, E reaches 4 MV/cm, while in the InGaN/GaN superlattices, values as high as E ≈ 6.5 MV/cm are found. The strong electric fields are caused by spontaneous and piezoelectric polarizations, the latter contribution dominating in InGaN/GaN superlattices. The influence of different arrangements of In atoms (indium clustering) on the band gap values in InGaN/GaN superlattices is examined.

  20. Cosmological N-body Simulation

    NASA Astrophysics Data System (ADS)

    Lake, George

    1994-05-01

    .90ex> }}} The ``N'' in N-body calculations has doubled every year for the last two decades. To continue this trend, the UW N-body group is working on algorithms for the fast evaluation of gravitational forces on parallel computers and establishing rigorous standards for the computations. In these algorithms, the computational cost per time step is ~ 10(3) pairwise forces per particle. A new adaptive time integrator enables us to perform high quality integrations that are fully temporally and spatially adaptive. SPH--smoothed particle hydrodynamics will be added to simulate the effects of dissipating gas and magnetic fields. The importance of these calculations is two-fold. First, they determine the nonlinear consequences of theories for the structure of the Universe. Second, they are essential for the interpretation of observations. Every galaxy has six coordinates of velocity and position. Observations determine two sky coordinates and a line of sight velocity that bundles universal expansion (distance) together with a random velocity created by the mass distribution. Simulations are needed to determine the underlying structure and masses. The importance of simulations has moved from ex post facto explanation to an integral part of planning large observational programs. I will show why high quality simulations with ``large N'' are essential to accomplish our scientific goals. This year, our simulations have N >~ 10(7) . This is sufficient to tackle some niche problems, but well short of our 5 year goal--simulating The Sloan Digital Sky Survey using a few Billion particles (a Teraflop-year simulation). Extrapolating past trends, we would have to ``wait'' 7 years for this hundred-fold improvement. Like past gains, significant changes in the computational methods are required for these advances. I will describe new algorithms, algorithmic hacks and a dedicated computer to perform Billion particle simulations. Finally, I will describe research that can be enabled by

  1. PARTITIONING THE RELATIVE INFLUENCE OF SOIL N, MYCORRHIZAE, AND FOLIAR N UPTAKE ON FOLIAR δ15N PATTERNS: CAN WE DETECT FOLIAR UPTAKE OF REACTIVE N?

    NASA Astrophysics Data System (ADS)

    Vallano, D.; Sparks, J. P.

    2009-12-01

    Vegetation is an important sink for atmospheric reactive N in N-limited systems and may be capable of incorporating reactive N compounds directly into leaves through the foliar uptake pathway. A proxy for atmospheric reactive N entering vegetation would be useful to estimate the impact of direct foliar N uptake on plant metabolism. Natural abundance foliar N isotopic composition (δ15N) is a practical tool for this purpose because plant-available N sources often have different isotopic compositions. Current understanding of foliar δ15N suggests these values primarily represent the integration of soil δ15N, direct foliar N uptake, mycorrhizal fractionation, and within-plant fractionations. Using a potted plant mesocosm system, we estimated the influence of mycorrhizae on foliar δ15N patterns in red maple (Acer rubrum) seedlings along an N deposition gradient in New York State. We found that mycorrhizal associations altered foliar δ15N in red maple seedlings from 0.03 - 1.01‰ across sites. Along the same temporal and spatial scales, we examined the influence of soil δ15N, foliar N uptake, and mycorrhizae on foliar δ15N in adult stands of American beech (Fagus grandifolia), black birch (Betula lenta), red maple (A. rubrum), and red oak (Quercus rubra). Using multiple regression models, atmospheric NO2 concentration explained 0%, 69%, 23%, and 45% of the residual variation in foliar δ15N remaining in American beech, red maple, red oak, and black birch, respectively, after accounting for soil δ15N. Our results suggest that foliar δ15N may be used to estimate pollution-derived atmospheric reactive N entering vegetation via the foliar N uptake pathway.

  2. N-chlorinated poly(N-isopropylacrylamide) microgels.

    PubMed

    Wang, Zuohe; Lam, Wing Yan; Pelton, Robert

    2013-10-22

    The treatment of poly(N-isopropylacrylamide) (PNIPAM) microgels with aqueous bleach (NaClO) at pH 10.5 resulted in the partial conversion of the amide hydrogen to the corresponding chloramide. N-Chlorinated microgels poly(NIPAM-co-NIPAMCl) are more hydrophobic than the parent PNIPAM microgels. Thus, the volume phase transition temperature decreases with increasing chlorination. During chlorination, the microgels coagulate once they undergo a volume phase transition. The chlorination reaction stops once the microgels dehydrate and coagulate, presumably as a result of the decreased diffusion rate of the ClO(-) anion into the microgels. The microgels are reversibly dechlorinated by glutathione (GSH), first giving PNIPAM shell + poly(NIPAM-co-NIPAMCl) core microgels. Because GSH is an important redox actor in biological cells, this work suggests that chlorinated microgels may be employed to deliver active chlorine to targeted cells.

  3. Equilibrium among potassium polytellurides in N,N-dimethylformamide solution

    NASA Astrophysics Data System (ADS)

    McAfee, Jason L.; Andreatta, Jeremy R.; Sevcik, Richard S.; Schultz, Linda D.

    2012-08-01

    Reactions between elemental potassium and tellurium in N,N-dimethylformamide (DMF) are monitored using UV-visible spectroscopy and compared with those in liquid ammonia solution. In liquid ammonia, the elements react together, via a step-wise sequence, to form polytellurides, each of which is characterized by a distinctive color, the highest being potassium tritelluride. However, when the elements are combined in DMF, these distinctive color changes are not observed - the solution develops an initial plum color, which gradually darkens to purple as the reaction progresses. UV-visible and Raman spectroscopic studies indicate that equilibrium exists among the mono-, di-, and tritelluride in DMF. This equilibrium is not seen in liquid ammonia solution due to the insolubility of potassium monotelluride in that solvent. Spectral data also indicate that potassium tetratelluride is formed in DMF solution.

  4. Antigenotoxicity of galangin against N-methyl-N-nitrosourea.

    PubMed

    Sohn, S J; Huh, I H; Au, W W; Heo, M Y

    1998-06-18

    Using the Ames bacterial mutagenicity test and an in vivo micronucleus test, we investigated the antigenotoxic effect of galangin against the genotoxicity of N-methyl-N-nitrosourea (MNU). In the Ames assay, galangin showed an antimutagenic effect towards MNU-induced mutagenicity of Salmonella typhimurium TA 100. In mice, galangin showed an anticlastogenic effect against MNU-induced micronuclei in polychromatic erythrocytes in the MNPCE in mouse bone marrow cells. On the other hand, galangin is neither mutagenic nor clastogenic in both assays. Results from our in vitro and in vivo studies indicate that galangin is capable of suppressing the mutagenicity and clastogenicity of MNU. Therefore, galangin may be a useful chemopreventive agent against potential long-term health effects from genotoxic environmental agents.

  5. Comprehensive extraction study using N,N-dioctyldiglycolamic acid.

    PubMed

    Shimojo, Kojiro; Nakai, Ayaka; Okamura, Hiroyuki; Saito, Takumi; Ohashi, Akira; Naganawa, Hirochika

    2014-01-01

    We report on the acid dissociation constants (Ka) of diglycolamic acid-type ligands together with comprehensive data on the extraction performance of N,N-dioctyldiglycolamic acid (DODGAA) for 54 metal ions. The pKa of the diglycolamic acid framework was determined to be 3.54 ± 0.03 in water (0.1 M LiCl, 25°C) by potentiometric titration, indicating that DODGAA is strongly acidic compared with acetic acid. DODGAA can quantitatively transfer various metal ions among the 54 metal ions through a proton-exchange reaction, and provides excellent extraction performance and separation ability for rare-earth metal ions, In(III), Fe(III), Hg(II), and Pb(II) among the 54 metal ions.

  6. Synthesis of symmetrical and unsymmetrical N,N'-diaryl guanidines via copper/N-methylglycine-catalyzed arylation of guanidine nitrate.

    PubMed

    Xing, Hui; Zhang, Ye; Lai, Yisheng; Jiang, Yongwen; Ma, Dawei

    2012-06-15

    CuI/N-methylglycine-catalyzed coupling reaction of guanidine nitrate with both aryl iodides and bromides takes place at 70-100 °C, affording symmetrical N,N'-diaryl guanidines with good to excellent yields. Unsymmetrical N,N'-diaryl guanidines can be assembled via monoarylation of guanidine nitrate with aryl iodides bearing a strong electron-withdrawing group and subsequent coupling with another aryl iodide.

  7. Neutron capture and (n,2n) measurements on 241Am

    SciTech Connect

    Vieira, D; Jandel, M; Bredeweg, T; Bond, E; Clement, R; Couture, A; Haight, R; O'Donnell, J; Reifarth, R; Ullmann, J; Wilhelmy, J; Wouters, J; Tonchev, A; Hutcheson, A; Angell, C; Crowell, A; Fallin, B; Hammond, S; Howell, C; Karowowski, H; Kelley, J; Pedroni, R; Tornow, W; Macri, R; Agvaanluvsan, U; Becker, J; Dashdorj, D; Stoyer, M; Wu, C

    2007-07-18

    We report on a set of neutron-induced reaction measurements on {sup 241}Am which are important for nuclear forensics and advanced nuclear reactor design. Neutron capture measurements have been performed on the DANCE detector array at the Los Alamos Neutron Scattering CEnter (LANSCE). In general, good agreement is found with the most recent data evaluations up to an incident neutron energy of {approx} 300 keV where background limits the measurement. Using mono-energetic neutrons produced in the {sup 2}H(d,n){sup 3}He reaction at Triangle University Nuclear Laboratory (TUNL), we have measured the {sup 241}Am(n,2n) excitation function from threshold (6.7 MeV) to 14.5 MeV using the activation method. Good agreement is found with previous measurements, with the exception of the three data points reported by Perdikakis et al. around 11 MeV, where we obtain a much lower cross section that is more consistent with theoretical estimates.

  8. A Detailed Chemical Kinetic Reaction Mechanism for n-Alkane Hydrocarbons From n-Octane to n-Hexadecane

    SciTech Connect

    Westbrook, C K; Pitz, W J; Herbinet, O; Curran, H J; Silke, E J

    2008-02-08

    Detailed chemical kinetic reaction mechanisms have been developed to describe the pyrolysis and oxidation of nine n-alkanes larger than n-heptane, including n-octane (n-C{sub 8}H{sub 18}), n-nonane (n-C{sub 9}H{sub 20}), n-decane (n-C{sub 10}H{sub 22}), n-undecane (n-C{sub 11}H{sub 24}), n-dodecane (n-C{sub 12}H{sub 26}), n-tridecane (n-C{sub 13}H{sub 28}), n-tetradecane (n-C{sub 14}H{sub 30}), n-pentadecane (n-C{sub 15}H{sub 32}), and n-hexadecane (n-C{sub 16}H{sub 34}). These mechanisms include both high temperature and low temperature reaction pathways. The mechanisms are based on our previous mechanisms for the primary reference fuels n-heptane and iso-octane, using the reaction class mechanism construction first developed for n-heptane. Individual reaction class rules are as simple as possible in order to focus on the parallelism between all of the n-alkane fuels included in the mechanisms, and these mechanisms will be refined further in the future to incorporate greater levels of accuracy and predictive capability. These mechanisms are validated through extensive comparisons between computed and experimental data from a wide variety of different sources. In addition, numerical experiments are carried out to examine features of n-alkane combustion in which the detailed mechanisms can be used to compare reactivities of different n-alkane fuels. The mechanisms for all of these n-alkanes are presented as a single detailed mechanism, which can be edited to produce efficient mechanisms for any of the n-alkanes included, and the entire mechanism, with supporting thermochemical and transport data, together with an explanatory glossary explaining notations and structural details, will be available for download from our web page.

  9. Polyamines. III. Spectroscopic properties of N, N-bis-(phthalimidopropyl)- N-octylamine and supramolecular interactions in its crystals

    NASA Astrophysics Data System (ADS)

    Brycki, Bogumił; Werner, Justyna; Kowalczyk, Iwona; Borowiak, Teresa; Wolska, Irena

    2010-04-01

    A new derivative of polyamine, N, N-bis-(phthalimidopropyl)- N-octylamine has been synthesized and its structure studied by X-ray diffraction, FTIR, 1H and 13C NMR spectroscopy. The B3LYP and DFT calculations have been carried out. The molecular conformation of N, N-bis-(phthalimidopropyl)- N-octylamine is folded and stabilized by an intramolecular C sbnd H⋯O hydrogen bond. A close similarity to the conformation of N, N-bis-(phthalimidopropyl)- N-propylamine has been found. The both molecules differ by the length of the saturated chains on the N-amine atom. The long N-octyl chain substituent gives rise to the supramolecular structure which is different to that one formed by the N-propyl derivative. The supramolecular structure is driven by weak C sbnd H⋯O and π⋯ π interactions. The optimized bond lengths as well as bond angles for N, N-bis-(phthalimidopropyl)- N-octylamine calculated by B3LYP/6-31G(d,p) approach are compared with the X-ray data. The screening constants for 13C and 1H atoms have been calculated by the GIAO/B3LYP/6-31G(d,p) approach and analyzed. Linear correlations between the experimental 1H and 13C chemical shifts and the computed screening constants have been obtained.

  10. 40 CFR 721.10193 - 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts. 721.10193 Section 721.10193 Protection of... CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10193 1-Butanaminium,...

  11. 40 CFR 721.10193 - 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts. 721.10193 Section 721.10193 Protection of... CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10193 1-Butanaminium,...

  12. 40 CFR 721.10193 - 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts. 721.10193 Section 721.10193 Protection of... CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10193 1-Butanaminium,...

  13. Registration of N614, A3N615, N616, and N617 Shattercane Genetic Stocks with cytoplasmic or nuclear male-sterility and juicy or dry midribs

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Four shattercane [Sorghum bicolor subsp. drummondii (Nees ex Steud) de Wet & Harlan] genetic stocks, N614, A3N615, N616, N617 (Reg. No. XXX, PI 665683 to 665686), with A3 cytoplasmic male-sterility or nuclear male-sterility gene ms3 containing either juicy (dd) or dry (DD) culms were developed joint...

  14. 40 CFR 721.10193 - 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts. 721.10193 Section 721.10193 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New...

  15. Photochemical N-demethylation of alkaloids.

    PubMed

    Ripper, J A; Tiekink, E R; Scammells, P J

    2001-02-26

    Certain alkaloids were observed to undergo N-demethylation processes under photochemical conditions. Tropine, acetyltropine, tropinone, and atropine were cleanly N-demethylated upon treatment with tetraphenylporphin, oxygen, and light. Dextromethorphan also underwent a N-demethylation reaction, but reacted further to afford an imine. In contrast, 14-acyloxycodeinones underwent a photochemically induced tandem N-demethylation acyl migration.

  16. 15N Isotopic Crop Exchange Residue Studies Suggest that IPCC N Input Methodologies to Assess N2O-N Emissions Should be Reevaluated

    Technology Transfer Automated Retrieval System (TEKTRAN)

    It is difficult to quantify nitrogen (N) losses from agricultural systems to the environment, however we can use 15N isotopic techniques to conduct site specific studies to increase our knowledge about N management and fate. This manuscript synthesizes the review of two selected 15N isotopic studies...

  17. Reactive N emissions from beef cattle feedlots

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Large amounts of nitrogen (N) are fed to meet the nutritional needs of beef cattle in feedlots. However, only from 10 to 15% of fed N is retained in animals. Most N is excreted. Chemical and biological processes transform manure N into ammonia, nitrous oxide and nitrate. These reactive forms of ...

  18. 40 CFR 721.10193 - 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false 1-Butanaminium, N-(3-aminopropyl)-N-butyl-N-(2-carboxyethyl)-, N-coco acyl derivs., inner salts. 721.10193 Section 721.10193 Protection of... CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10193 1-Butanaminium,...

  19. "N"-2 Repetition Costs Depend on Preparation in Trials "n"-1 and "n"-2

    ERIC Educational Resources Information Center

    Scheil, Juliane; Kleinsorge, Thomas

    2014-01-01

    In task switching, a common result supporting the notion of inhibitory processes as a determinant of switch costs is the occurrence of "n"-2 repetition costs. Evidence suggests that this effect is not affected by preparation. However, the role of preparation on preceding trials has been neglected so far. In this study, evidence for an…

  20. Understanding the acid-base properties of adenosine: the intrinsic basicities of N1, N3 and N7.

    PubMed

    Kapinos, Larisa E; Operschall, Bert P; Larsen, Erik; Sigel, Helmut

    2011-07-11

    Adenosine (Ado) can accept three protons, at N1, N3, and N7, to give H(3) (Ado)(3+) , and thus has three macro acidity constants. Unfortunately, these constants do not reflect the real basicity of the N sites due to internal repulsions, for example, between (N1)H(+) and (N7)H(+). However, these macroconstants are still needed for the evaluations and the first two are taken from our own earlier work, that is, pK(H)(H(3))((Ado)) = -4.02 and pK(H)(H(2))((Ado)) = -1.53; the third one was re-measured as pK(H)(H)((Ado)) = 3.64 ± 0.02 (25 °C; I=0.5 M, NaNO(3)), because it is the main basis for evaluating the intrinsic basicities of N7 and N3. Previously, contradicting results had been published for the micro acidity constant of the (N7)H(+) site; this constant has now been determined in an unequivocal manner, and that of the (N3)H(+) site was obtained for the first time. The micro acidity constants, which describe the release of a proton from an (N)H(+) site under conditions for which the other nitrogen atoms are free and do not carry a proton, decrease in the order pk(N7-N1)(N7(Ado)N1·H)) = 3.63 ± 0.02 > pk(N7-N1)(H·N7(Ado)N1) = 2.15 ± 0.15 > pk(N3-N1,N7)(H·N3(Ado)N1,N7) =1.5 ± 0.3, reflecting the decreasing basicity of the various nitrogen atoms, that is, N1>N7>N3. Application of the above-mentioned microconstants allows one to calculate the percentages (formation degrees) of the tautomers formed for monoprotonated adenosine, H(Ado)(+) , in aqueous solution; the results are 96.1, 3.2, and 0.7% for N7(Ado)N1·H(+), (+)H·N7(Ado)N1, and (+)H·N3(Ado)N1,N7, respectively. These results are in excellent agreement with theoretical DFT calculations. Evidently, H(Ado)(+) exists to the largest part as N7(Ado)N1·H(+) having the proton located at N1; the two other tautomers are minority species, but they still form. These results are not only meaningful for adenosine itself, but are also of relevance for nucleic acids and adenine nucleotides, as they help to understand

  1. 100-N Area underground storage tank closures

    SciTech Connect

    Rowley, C.A.

    1993-08-01

    This report describes the removal/characterization actions concerning underground storage tanks (UST) at the 100-N Area. Included are 105-N-LFT, 182-N-1-DT, 182-N-2-DT, 182-N-3-DT, 100-N-SS-27, and 100-N-SS-28. The text of this report gives a summary of remedial activities. In addition, correspondence relating to UST closures can be found in Appendix B. Appendix C contains copies of Unusual Occurrence Reports, and validated sampling data results comprise Appendix D.

  2. Educación no formal

    NASA Astrophysics Data System (ADS)

    Tignanelli, H.

    Se comentan en esta comunicación, las principales contribuciones realizadas en el campo de la educación en astronomía en los niveles primario, secundario y terciario, como punto de partida para la discusión de la actual inserción de los contenidos astronómicos en los nuevos contenidos curriculares de la EGB - Educación General Básica- y Polimodal, de la Reforma Educativa. En particular, se discuten los alcances de la educación formal y no formal, su importancia para la capacitación de profesores y maestros, y perspectivas a futuro.

  3. A Detailed Chemical Kinetic Reaction Mechanism for n-Alkane Hydrocarbons from n-Octane to n-Hexadecane

    SciTech Connect

    Westbrook, C K; Pitz, W J; Herbinet, O; Silke, E J; Curran, H J

    2007-09-25

    Detailed chemical kinetic reaction mechanisms have been developed to describe the pyrolysis and oxidation of the n-alkanes, including n-octane (n-C{sub 8}H{sub 18}), n-nonane (n-C{sub 9}H{sub 20}), n-decane (n-C{sub 10}H{sub 22}), n-undecane (n-C{sub 11}H{sub 24}), n-dodecane (n-C{sub 12}H{sub 26}), n-tridecane (n-C{sub 13}H{sub 28}), n-tetradecane (n-C{sub 14}H{sub 30}), n-pentadecane (n-C{sub 15}H{sub 32}), and n-hexadecane (n-C{sub 16}H{sub 34}). These mechanisms include both high temperature and low temperature reaction pathways. The mechanisms are based on previous mechanisms for n-heptane, using the same reaction class mechanism construction developed initially for n-heptane. Individual reaction class rules are as simple as possible in order to focus on the parallelism between all of the n-alkane fuels included in the mechanisms, and there is an intent to develop these mechanisms further in the future to incorporate greater levels of accuracy and predictive capability. Several of these areas for improvement are identified and explained in detail. These mechanisms are validated through comparisons between computed and experimental data from as many different sources as possible. In addition, numerical experiments are carried out to examine features of n-alkane combustion in which the detailed mechanisms can be used to compare processes in all of the n-alkane fuels. The mechanisms for all of these n-alkanes are presented as a single detailed mechanism, which can be edited to produce efficient mechanisms for any of the n-alkanes included, and the entire mechanism, with supporting thermochemical and transport data, together with an explanatory glossary explaining notations and structural details, will be available on our web page when the paper is accepted for publication.

  4. Influence of InGaN sub-quantum-well on performance of InAlN/GaN/InAlN resonant tunneling diodes

    SciTech Connect

    Chen, Haoran; Yang, Lin'an Hao, Yue

    2014-08-21

    The resonant tunneling mechanism of the GaN based resonant tunneling diode (RTD) with an InGaN sub-quantum-well has been investigated by means of numerical simulation. At resonant-state, Electrons in the InGaN/InAlN/GaN/InAlN RTD tunnel from the emitter region through the aligned discrete energy levels in the InGaN sub-quantum-well and GaN main-quantum-well into the collector region. The implantation of the InGaN sub-quantum-well alters the dominant transport mechanism, increase the transmission coefficient and give rise to the peak current and peak-to-valley current ratio. We also demonstrate that the most pronounced negative-differential-resistance characteristic can be achieved by choosing appropriately the In composition of In{sub x}Ga{sub 1−x}N at around x = 0.06.

  5. Microcosm N2O emissions wth calibration

    EPA Pesticide Factsheets

    The dataset consists of measurements of soil nitrous oxide emissions from soils under three different amendments: glucose, cellulose, and manure. Data includes the four isotopomers of nitrous oxide (14N15N16O, 15N14N16O, 14N14N18O, 14N14N16O), and the site preference.This dataset is associated with the following publication:Chen , H., D. Williams , P. Deshmukh , F. Birgand, B. Maxwell, and J. Walker. Probing the Biological Sources of Soil N2O Emissions by Quantum Cascade Laser-Based 15N Isotopocule Analysis. SOIL SCIENCE SOCIETY OF AMERICA JOURNAL. Soil Science Society of America, Madison, WI, USA, 100(0): 175-181, (2016).

  6. Reflections on the "N" + "k" Queens Problem

    ERIC Educational Resources Information Center

    Chatham, Doug

    2009-01-01

    The "N" queens problem is a classic puzzle. It asks for an arrangement of "N" mutually non-attacking queens on an "N" x "N" chessboard. We discuss a recent variation called the "N" + "k" queens problem, where pawns are added to the chessboard to allow a greater number of non-attacking queens to be placed on it. We describe some of what is known…

  7. N=1 supersymmetric {beta}-functions

    SciTech Connect

    Jones, D. R. T.

    1997-06-15

    Recent results on three-loop, four-loop and large-N{sub f}{beta}-functions in supersymmetric gauge theories are summarised. It is argued that the O(1/N{sub f})-corrected form of {beta}{sub g} in SQCD is consistent with the existence of the conformal window 3N{sub c}/2<N{sub f}<3N{sub c}.

  8. Effects of GaN/AlGaN/Sputtered AlN nucleation layers on performance of GaN-based ultraviolet light-emitting diodes

    PubMed Central

    Hu, Hongpo; Zhou, Shengjun; Liu, Xingtong; Gao, Yilin; Gui, Chengqun; Liu, Sheng

    2017-01-01

    We report on the demonstration of GaN-based ultraviolet light-emitting diodes (UV LEDs) emitting at 375 nm grown on patterned sapphire substrate (PSS) with in-situ low temperature GaN/AlGaN nucleation layers (NLs) and ex-situ sputtered AlN NL. The threading dislocation (TD) densities in GaN-based UV LEDs with GaN/AlGaN/sputtered AlN NLs were determined by high-resolution X-ray diffraction (XRD) and cross-sectional transmission electron microscopy (TEM), which revealed that the TD density in UV LED with AlGaN NL was the highest, whereas that in UV LED with sputtered AlN NL was the lowest. The light output power (LOP) of UV LED with AlGaN NL was 18.2% higher than that of UV LED with GaN NL owing to a decrease in the absorption of 375 nm UV light in the AlGaN NL with a larger bandgap. Using a sputtered AlN NL instead of the AlGaN NL, the LOP of UV LED was further enhanced by 11.3%, which is attributed to reduced TD density in InGaN/AlInGaN active region. In the sputtered AlN thickness range of 10–25 nm, the LOP of UV LED with 15-nm-thick sputtered AlN NL was the highest, revealing that optimum thickness of the sputtered AlN NL is around 15 nm. PMID:28294166

  9. Effects of GaN/AlGaN/Sputtered AlN nucleation layers on performance of GaN-based ultraviolet light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Hu, Hongpo; Zhou, Shengjun; Liu, Xingtong; Gao, Yilin; Gui, Chengqun; Liu, Sheng

    2017-03-01

    We report on the demonstration of GaN-based ultraviolet light-emitting diodes (UV LEDs) emitting at 375 nm grown on patterned sapphire substrate (PSS) with in-situ low temperature GaN/AlGaN nucleation layers (NLs) and ex-situ sputtered AlN NL. The threading dislocation (TD) densities in GaN-based UV LEDs with GaN/AlGaN/sputtered AlN NLs were determined by high-resolution X-ray diffraction (XRD) and cross-sectional transmission electron microscopy (TEM), which revealed that the TD density in UV LED with AlGaN NL was the highest, whereas that in UV LED with sputtered AlN NL was the lowest. The light output power (LOP) of UV LED with AlGaN NL was 18.2% higher than that of UV LED with GaN NL owing to a decrease in the absorption of 375 nm UV light in the AlGaN NL with a larger bandgap. Using a sputtered AlN NL instead of the AlGaN NL, the LOP of UV LED was further enhanced by 11.3%, which is attributed to reduced TD density in InGaN/AlInGaN active region. In the sputtered AlN thickness range of 10–25 nm, the LOP of UV LED with 15-nm-thick sputtered AlN NL was the highest, revealing that optimum thickness of the sputtered AlN NL is around 15 nm.

  10. Reactions of ions in excited electronic states - Excited N2/+/ ion reacting with N2 to yield N3/+/ and N

    NASA Technical Reports Server (NTRS)

    Bowers, M. T.; Kemper, P. R.; Laudenslager, J. B.

    1974-01-01

    Study of the mechanism of formation of the N3(+) ion from the bimolecular reaction of excited N2(+) ions in gaseous N2. Using ion cyclotron resonance spectroscopy, an attempt is made to inquire more deeply than hitherto into the origin of the N3(+) ions and to determine the rate constant for their formation and the limits on the lifetime of the reactant excited N2(+) ions.

  11. Materials considerations for molten salt accelerator-based plutonium conversion systems

    SciTech Connect

    DeVan, J.H.; DiStefano, J.R.; Eatherly, W.P.; Keiser, J.R.; Klueh, R.L.

    1994-12-31

    A Molten-Salt Reactor Program for power applications was initiated at the Oak Ridge National Laboratory in 1956. In 1965 the Molten Salt Reactor Experiment (MSRE) went critical and was successfully operated for several years. Operation of the MSRE revealed two deficiencies in the Hastelloy N alloy that had been developed specifically for molten-salt systems. The alloy embrittled at elevated temperatures as a result of exposure to thermal neutrons (radiation damage) and grain boundary embrittlement occurred in materials to fuel salt. Intergranular cracking was found to be associated with fission products, viz. tellurium. An improved Hastelloy N composition was subsequently developed that had better resistance to both of these problems. However, the discovery that fission product cracking could be significantly decreased by making the salt sufficiently reducing offers the prospect of improved compatibility with molten salts containing fission products and resistance to radiation damage in ABC applications. Recommendations are made regarding the types of corrosion tests and mechanistic studies needed to qualify materials for operation with PuF{sub 3}-containing molten salts.

  12. Materials corrosion in molten LiF-NaF-KF eutectic salt under different reduction-oxidation conditions

    SciTech Connect

    Sellers, R. S.; Cheng, W. J.; Anderson, M. H.; Sridharan, K.; Wang, C. J.; Allen, T. R.

    2012-07-01

    Molten fluoride salts such as FLiNaK (LiF-NaF-KF: 46.5-11.5-42 mol %) have been proposed for use as secondary reactor coolants, media for transfer of high temperature process heat from nuclear reactors to chemical plants, and for concentrated solar power thermal energy storage. In molten fluoride salts, passive oxide films are chemically unstable, and corrosion is driven largely by the thermodynamically driven dissolution of alloying elements into the molten salt environment. Two alloys, Hastelloy{sup R} N and 316L stainless steel were exposed to molten FLiNaK salt in a 316L stainless steel crucible under argon cover gas for 1000 hours at 850 deg. C. Graphite was present in some of the crucibles with the goal of studying corrosion behavior of relevant reactor material combinations. In addition, a technique to reduce alloy corrosion through modification of the reduction-oxidation state was tested by the inclusion of zirconium to the system. Corrosion of 316L stainless steel was noted to occur primarily through surface depletion of chromium, an effect that was enhanced by the presence of graphite. Hastelloy{sup R} N experienced weight gain through electrochemical plating of corrosion products derived from the 316L stainless steel crucible. In the presence of zirconium, both alloys gained weight through plating of zirconium and as a result formed intermetallic layers. (authors)

  13. N+CPT clock resonance

    SciTech Connect

    Crescimanno, M.; Hohensee, M.

    2008-12-15

    In a typical compact atomic time standard a current modulated semiconductor laser is used to create the optical fields that interrogate the atomic hyperfine transition. A pair of optical sidebands created by modulating the diode laser become the coherent population trapping (CPT) fields. At the same time, other pairs of optical sidebands may contribute to other multiphoton resonances, such as three-photon N-resonance [Phys. Rev. A 65, 043817 (2002)]. We analyze the resulting joint CPT and N-resonance (hereafter N+CPT) analytically and numerically. Analytically we solve a four-level quantum optics model for this joint resonance and perturbatively include the leading ac Stark effects from the five largest optical fields in the laser's modulation comb. Numerically we use a truncated Floquet solving routine that first symbolically develops the optical Bloch equations to a prescribed order of perturbation theory before evaluating. This numerical approach has, as input, the complete physical details of the first two excited-state manifolds of {sup 87}Rb. We test these theoretical approaches with experiments by characterizing the optimal clock operating regimes.

  14. Quantum algebra of N superspace

    SciTech Connect

    Hatcher, Nicolas; Restuccia, A.; Stephany, J.

    2007-08-15

    We identify the quantum algebra of position and momentum operators for a quantum system bearing an irreducible representation of the super Poincare algebra in the N>1 and D=4 superspace, both in the case where there are no central charges in the algebra, and when they are present. This algebra is noncommutative for the position operators. We use the properties of superprojectors acting on the superfields to construct explicit position and momentum operators satisfying the algebra. They act on the projected wave functions associated to the various supermultiplets with defined superspin present in the representation. We show that the quantum algebra associated to the massive superparticle appears in our construction and is described by a supermultiplet of superspin 0. This result generalizes the construction for D=4, N=1 reported recently. For the case N=2 with central charges, we present the equivalent results when the central charge and the mass are different. For the {kappa}-symmetric case when these quantities are equal, we discuss the reduction to the physical degrees of freedom of the corresponding superparticle and the construction of the associated quantum algebra.

  15. Investigation of Gd3N@C2n (40 <= n <= 44) family by Raman and inelastic electron tunneling spectroscopy

    NASA Astrophysics Data System (ADS)

    Burke, Brian; Chan, Jack; Williams, Keith; Ge, Jiechao; Shu, Chunying; Fu, Wujun; Dorn, Harry; Kushmerick, James; Puretzky, Alexander; Geohegan, David

    2010-03-01

    The structure and vibrational spectrum of Gd3N@C80 is studied through Raman and inelastic electron tunneling spectroscopy (IETS) as well as density functional theory (DFT) and universal force field (UFF) calculations. Hindered rotations, shown by both theory and experiment, indicate the formation of a Gd3N-C80 bond which reduces the ideal icosahedral symmetry of the C80 cage. The vibrational modes involving the movement of the encapsulated species are a fingerprint of the interaction between the fullerene cage and the core complex. We present Raman data for the Gd3N@C2n (40 <= n <= 44) family as well as Y3N@C80, Lu3N@C80, and Y3N@C88 for comparison. Conductance measurements have been performed on Gd3N@C80 and reveal a Kondo effect similar to that observed in C60.

  16. Elimination of surface band bending on N-polar InN with thin GaN capping

    SciTech Connect

    Kuzmík, J. Haščík, Š.; Kučera, M.; Kúdela, R.; Dobročka, E.; Adikimenakis, A.; Mičušík, M.; Gregor, M.; Plecenik, A.; Georgakilas, A.

    2015-11-09

    0.5–1 μm thick InN (0001) films grown by molecular-beam epitaxy with N- or In-polarity are investigated for the presence of native oxide, surface energy band bending, and effects introduced by 2 to 4 monolayers of GaN capping. Ex situ angle-resolved x-ray photo-electron spectroscopy is used to construct near-surface (GaN)/InN energy profiles, which is combined with deconvolution of In3d signal to trace the presence of InN native oxide for different types of polarity and capping. Downwards surface energy band bending was observed on bare samples with native oxide, regardless of the polarity. It was found that the In-polar InN surface is most readily oxidized, however, with only slightly less band bending if compared with the N-polar sample. On the other hand, InN surface oxidation was effectively mitigated by GaN capping. Still, as confirmed by ultra-violet photo-electron spectroscopy and by energy band diagram calculations, thin GaN cap layer may provide negative piezoelectric polarization charge at the GaN/InN hetero-interface of the N-polar sample, in addition to the passivation effect. These effects raised the band diagram up by about 0.65 eV, reaching a flat-band profile.

  17. Nitrogen input 15N-signatures are reflected in plant 15N natural abundances of N-rich tropical forest in China

    NASA Astrophysics Data System (ADS)

    Abdisa Gurmesa, Geshere; Lu, Xiankai; Gundersen, Per; Yunting, Fang; Mo, Jiangming

    2016-04-01

    In this study, we tested the measurement of natural abundance of 15N (δ15N) for its ability to assess changes in N cycling due to increased N deposition in two forest types; namely, an old-growth broadleaved forest and a pine forest, in southern China. We measured δ15N values of inorganic N in input and output fluxes under ambient N deposition, and N concentration and δ15N of major ecosystem compartments under ambient and increased N deposition. Our results showed that N deposition to the forests was 15N-depleted, and was dominated by NH4-N. Plants were 15N-depleted due to imprint from the 15N-depleted atmospheric N deposition. The old-growth forest had larger N concentration and was more 15N-enriched than the pine forest. Nitrogen addition did not significantly affect N concentration, but it significantly increased δ15N values of plants, and slightly more so in the pine forest, toward the 15N signature of the added N in both forests. The result indicates that the pine forest may rely more on the 15N-depleted deposition N. Soil δ15N values were slightly decreased by the N addition. Our result suggests that ecosystem δ15N is more sensitive to the changes in ecosystem N status and N cycling than N concentration in N-saturated sub-tropical forests.

  18. Surface donor states distribution post SiN passivation of AlGaN/GaN heterostructures

    SciTech Connect

    Goyal, Nitin; Fjeldly, Tor A.

    2014-07-21

    In this paper, we present a physics based analytical model to describe the effect of SiN passivation on two-dimensional electron gas density and surface barrier height in AlGaN/GaN heterostructures. The model is based on an extraction technique to calculate surface donor density and surface donor level at the SiN/AlGaN interface. The model is in good agreement with the experimental results and promises to become a useful tool in advanced design and characterization of GaN based heterostructures.

  19. [Spatial Variation of Ammonia-N, Nitrate-N and Nitrite-N in Groundwater of Dongshan Island].

    PubMed

    Wiu, Hai-yan; Fu, Shi-feng; Cai, Xiao-qiong; Tang, Kun-xian; Cao, Chao; Chen, Qing-hui; Liang, Xiu-yu

    2015-09-01

    In Dongshan Island, groundwater is the main resource of the local residents' drinking water, domestic water, agriculture irrigation and freshwater aquaculture. This study aimed to investigate the spatial distribution characteristic and its variation pattern of ammonia-N, nitrate-N and nitrite-N in groundwater, as well as its pollution source and influence factors. It is very important to understand the pollution level of ammonia-N, nitrate-N and nitrite-N in groundwater of Dongshan Island, the control and prevention of ammonia-N, nitrate-N and nitrite-N pollution, which is of great significance to the residents' health. In this study, the spatial variability characteristics of ammonia-N, nitrate-N and nitrite-N concentration in groundwater of Dongshan Island was analysed by geo- statistic method, the values of the non-observation points were determined by Kriging method, and the pollution characteristics of ammonia-N, nitrate-N and nitrite-N in groundwater of Dongshan Island was also analyzed. Our results showed that the ammonia-N and nitrite-N concentration in groundwater of Dongshan Island were at low levels, but their spatial variability were high, and their autocorrelation were poor; however, the nitrate-N concentration was general high, its spatial variability was moderate, and the autocorrelation was much good. The distribution characteristics of ammonia-N, nitrate-N and nitrite-N in groundwater of Dongshan Island were similar that the high concentration areas were all located in the coastal land. The domestic pollutants and human and animal wastes from towns and villages were the main sources of nitrogen pollution, which would be the first step to control the nitrogen pollution of Dongshan Island. Land use pattern, soil type, groundwater depth, pH, dissolved oxygen, season, and the existence of Fe2+, were the impact factors that influence the distribution and transformation of ammonia-N, nitrate-N and nitrite-N in groundwater, which could be the considerable

  20. Simultaneous determination of N-hydroxymethyl-N-methylformamide, N-methylformamide and N-acetyl-S-(N-methylcarbamoyl)cystein in urine samples from workers exposed to N,N-dimethylformamide by liquid chromatography-tandem mass spectrometry.

    PubMed

    Sohn, Jae Ho; Han, Min Jeong; Lee, Mi Young; Kang, Seong-Kyu; Yang, Jeong Sun

    2005-02-07

    N-Hydroxymethyl-N-methylformamide (HMMF) and N-methylformamide (NMF) in urine samples from workers exposed to N,N-dimethylformamide (DMF) cannot be distinguished by a gas chromatographic method because HMMF is converted to NMF at the injection port of gas chromatography (GC). Total NMF (HMMF+NMF) has been measured instead. Also, the determination of N-acetyl-S-(N-methylcarbamoyl)cystein (AMCC), which is supposed to be related to the toxicity of DMF, needs multiple treatments to convert to a volatile compound before GC analysis. There is no previous report of a simultaneous determination of three major metabolites of DMF in urine. The aim of this study is to develop a simple and selective method for the determination of DMF metabolite in urine. By using a liquid chromatography-tandem mass spectrometry, we can directly distinguish these three major metabolites of DMF in a single run. The diluted urine samples were analyzed on Capcell Pak MF SG80 column with the mobile phase of methanol in 2mM formic acid (10:90, v/v). The analytes were detected by an electrospray ionization tandem mass spectrometry in the multiple-reaction-monitoring mode. The standard curves were linear (r>0.999) over the concentration ranges of 0.004-8 microg/mL. The precision and accuracy of quality control samples for inter-batch (n=6) analyses were in the range of 1.3-9.8% and 94.7-116.8, respectively. The sum of each HMMF and NMF concentration determined by LC-MS/MS method shows high correlation (r=0.9927 with the slope of 1.0415, p<0.0001) with NMF included HMMF concentration determined by GC method for 13 urine samples taken from workers exposed to DMF. The excretion ratio of HMMF:NMF:AMCC is approximately 4:1:1 in molar concentration.

  1. HVPE-GaN growth on GaN-based Advanced Substrates by Smart Cut™

    NASA Astrophysics Data System (ADS)

    Iwinska, M.; Amilusik, M.; Fijalkowski, M.; Sochacki, T.; Lucznik, B.; Grzanka, E.; Litwin-Staszewska, E.; Weyher, J. L.; Nowakowska-Siwinska, A.; Muziol, G.; Skierbiszewski, C.; Grzegory, I.; Guiot, E.; Caulmilone, R.; Bockowski, M.

    2016-12-01

    Advanced Substrates consist of a thin GaN layer bonded to a carrier wafer. The layer is separated from starting material by Smart Cut™ technology. GaN on sapphire Advanced Substrates were successfully used as seeds for HVPE-GaN growth. Unintentionally doped and silicon-doped thick GaN layers were crystallized. The results were compared to HVPE-GaN grown on standard MOCVD-GaN/sapphire templates. Free-standing HVPE-GaN with high free carrier concentration was obtained. A laser diode was built on the n-type doped HVPE-GaN grown on an Advanced Substrate.

  2. AlGaN-Cladding-Free m-Plane InGaN/GaN Laser Diodes with p-Type AlGaN Etch Stop Layers

    NASA Astrophysics Data System (ADS)

    Farrell, Robert M.; Haeger, Daniel A.; Hsu, Po Shan; Hardy, Matthew T.; Kelchner, Kathryn M.; Fujito, Kenji; Feezell, Daniel F.; Mishra, Umesh K.; DenBaars, Steven P.; Speck, James S.; Nakamura, Shuji

    2011-09-01

    We present a new method of improving the accuracy and reproducibility of dry etching processes for ridge waveguide InGaN/GaN laser diodes (LDs). A GaN:Al0.09Ga0.91N etch rate selectivity of 11:1 was demonstrated for an m-plane LD with a 40 nm p-Al0.09Ga0.91N etch stop layer (ESL) surrounded by Al-free cladding layers, establishing the effectiveness of AlGaN-based ESLs for controlling etch depth in ridge waveguide InGaN/GaN LDs. These results demonstrate the potential for integrating AlGaN ESLs into commercial device designs where accurate control of the etch depth of the ridge waveguide is necessary for stable, kink-free operation at high output powers.

  3. Ntrace a 15N tracing model to analyse gross N transformations and sources of gaseous N emissions

    NASA Astrophysics Data System (ADS)

    Muller, Christoph

    2013-04-01

    Anthropogenically generated reactive nitrogen (N) cascades throughout the global environment ...(Galloway and Cowling, 2002). This reactive N may be lost from ecosystems via leaching, as nitrate (NO3-), or in gaseous forms such as ammonia and nitrous oxide (N2O) and the loss is governed by the N dynamics of the system. Thus, to be rendered environmentally benign NO3- must be reduced to a non-reactive form, dinitrogen (N2) which requires the evaluation of three major biological pathways of NO3- reduction: i) assimilatory NO3- reduction into biomass, ii) dissimilatory NO3- reduction to NH4+ (DNRA) and iii) dissimilatory NO3- reduction to N2 (denitrification) ...(Burger and Jackson, 2004). Advanced techniques based on 15N tracing in combination with suitable model analyses are the method of choice to analyse complex N interactions and simultaneous N transformation process. Techniques are based on dilution - enrichment principles and usually rely on the simultaneous labelling of various N pools. The data sets are then analysed by suitable 15N tracing models which allow the individual N transformation rates to be calculated based on realistic kinetic settings. The 15N tracing model Ntrace has been developed to analyse the simultaneously occurring N transformation rates in soil-plant systems and includes submodels for the evaluation of the processes associated with gaseous N emissions. The 15N tracing model and some typical model results will be presented. Literature cited .Burger, M., and Jackson, L. E. (2004). Plant and microbial use and turnover: rapid conversion of nitrate to ammonium in soil with roots. Plant and Soil 266, 289-301. Galloway, J. N., and Cowling, E. B. (2002). Reactive nitrogen and the world: 200 years of change. Ambio 31, 64-71. .

  4. A taxonomic revision of Neoserica (sensu lato): the species groups N. lubrica, N. obscura, and N. silvestris (Coleoptera, Scarabaeidae, Sericini)

    PubMed Central

    Liu, Wan-Gang; Fabrizi, Silvia; Bai, Ming; Ahrens, Dirk

    2016-01-01

    Abstract The species of the Neoserica lubrica Brenske, 1898, Neoserica obscura (Blanchard, 1850) and Neoserica silvestris Brenske, 1902 species groups are revised. The study resulted in the following new synonymies and combinations: Neoserica obscura (Blanchard, 1850) = Microserica roeri Frey, 1972, syn. n., = Maladera chinensis (Arrow, 1946), syn. n.; Neoserica hainana (Brenske, 1898), comb. n., and Neoserica minor (Arrow, 1946), comb. n. The known species are redescribed. The following nine new species are described from China: Neoserica allobscura Ahrens, Fabrizi & Liu, sp. n., Neoserica dongjiafenensis Ahrens, Fabrizi & Liu, sp. n., Neoserica fugongensis Ahrens, Fabrizi & Liu, sp. n., Neoserica mantillerii Ahrens, Fabrizi & Liu, sp. n., Neoserica menglunensis Ahrens, Fabrizi & Liu, sp. n., Neoserica pseudosilvestris Ahrens, Fabrizi & Liu, sp. n., Neoserica sakoliana Ahrens, Fabrizi & Liu, sp. n., Neoserica shuyongi Ahrens, Fabrizi & Liu, sp. n., and Neoserica tahianensis Ahrens, Fabrizi & Liu, sp. n. A key to the Sericini genera with multilamellate antenna, species groups of Neoserica of mainland Asia, and species of the species groups examined here are provided. Maps of the species distribution are provided, habitus and male genitalia are illustrated. PMID:27917061

  5. Variation in internal N efficiency of maize and impact on yield-goal based N recommendations

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Internal N efficiency (IE) is defined as grain dry matter (DM) produced per unit of N in the above-ground plant at physiological maturity (R6). Internal N efficiency defines the target for plant N content at R6 in yield-goal based N rate recommendations (currently used in 30 U.S. states) and several...

  6. 40 CFR Table 1 to Subpart N of... - General Provisions Applicability to Subpart N

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Subpart N 1 Table 1 to Subpart N of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Electroplating and Chromium Anodizing Tanks Pt. 63, Subpt. N, Table 1 Table 1 to Subpart N of Part 63—General...) No § 63.347(g) and (h) of subpart N specify the frequency of periodic reports of monitoring data...

  7. Eta(') mass and chiral symmetry breaking at large N(c) and N(f).

    PubMed

    Girlanda, L; Stern, J; Talavera, P

    2001-06-25

    We propose a method for implementing the large- N(c), large-N(f) limit of QCD at the effective Lagrangian level. Depending on the value of the ratio N(f)/N(c), different patterns of chiral symmetry breaking can arise, leading in particular to different behaviors of the eta(') mass in the combined large-N limit.

  8. Bioconjugation of quantum-dots with chitosan and N,N,N-trimethyl chitosan.

    PubMed

    Mansur, Herman S; Mansur, Alexandra A P; Curti, Elisabete; De Almeida, Mauro V

    2012-09-01

    Novel carbohydrate-based hybrids combining chitosan and chemically modified chitosan with CdS inorganic nanoparticles were designed and prepared via aqueous route at room temperature. N,N,N-trimethylchitosan (TM-chitosan) was synthesized aiming at substantially improving the water solubility of chitosan for producing stable colloidal systems. UV-vis spectroscopy, photoluminescence spectroscopy, Nuclear magnetic resonance spectroscopy, Raman spectroscopy, and Fourier transform infrared spectroscopy were used to characterize the synthesis and the relative stability of biopolymer-capped CdS nanocrystals. The results have clearly indicated that chitosan and chitosan-derivative (TM-chitosan) were remarkably effective on nucleating and stabilizing CdS nanoparticles in aqueous suspensions. In addition, the CdS nanocrystals were produced in the so-called "quantum-size confinement regime", with the calculated average size below 3.5 nm and fluorescent activity in the visible range of the spectra. Therefore, a new single-step process was developed for the bioconjugation of quantum dots with water soluble chemically functionalized carbohydrates at room temperature for potential biomedical applications.

  9. Is N,N-dimethylglycine N-oxide a choline and betaine metabolite?

    PubMed

    Lever, Michael; McEntyre, Christopher J; George, Peter M; Chambers, Stephen T

    2017-01-13

    Choline metabolism is by oxidation to betaine, which is demethylated to N,N-dimethylglycine; dimethylglycine is oxidatively demethylated to sarcosine. This pathway is important for osmoregulation and as a source of methyl groups. We asked whether another metabolite was involved. We synthesized the N-oxide of dimethylglycine (DMGO) by oxidizing dimethylglycine with peracetic acid, and measured DMGO in human plasma and urine by HPLC-MS/MS with positive ion detection, using two chromatography procedures, based on ion exchange and HILIC separations. The molecular ion DMGOH+ (m/z=120) yielded four significant fragments (m/z=103, 102, 58 and 42). The suspected DMGO peak in human body fluids showed all these fragments, and co-chromatographed with added standard DMGO in both HPLC systems. Typical plasma concentrations of DMGO are under 1 μmol/l. They may be lower in metabolic syndrome patients. Urine concentrations are higher, and DMGO has a higher fractional clearance than dimethylglycine, betaine and choline. It was present in all of over 80 human urine and plasma samples assayed. Plasma DMGO concentrations correlate with plasma DMG concentrations, with betaine and choline concentrations, with the osmolyte myo-inositol, and strongly with urinary DMGO excretion. We conclude that DMGO is probably a normal human metabolite.

  10. Mechanisms of intestinal absorption of the carcinogen MNNG (N-Methyl-N'-nitro-N-nitrosoguanidine)

    SciTech Connect

    Koyama, S.Y.; Hollander, D.; Dadufalza, V.

    1988-06-01

    The authors studied the characteristics and mechanisms of MNNG (N-methyl-N'-nitro-N-nitrosoguanidine) intestinal absorption and the interaction between bile acids and fatty acids and MNNG absorption rat in vivo in male Sprague-Dawley rats. They found that MNNG was absorbed by simple passive diffusion. Transport of MNNG was the highest at pH 6.0. The addition of the bile salt, taurocholate by itself, greatly increased MNNG absorption, while the addition of the long-chain unsaturated fatty acids, oleic and linoleic, decreased the rate of absorption of MNNG. The phospholipid lecithin addition to the perfusate did not change the rate of MNNG absorption. Induction of dietary vitamin A deficiency (serum vitamin A level decreased from 40.9 to 13.7 ..mu..g/dl) did not change the absorption rate of MNNG. These studies demonstrate that bile acids, dietary fatty acids, and the pH of the intestinal content can modify the rate of absorption of this carcinogen by the small intestine. Since initial intestinal absorption determines serum levels and subsequent reabsorption and enterohepatic cycling determines long-term lumenal levels, serum levels, and total body content, factors which modify the rate of intestinal absorption of MNNG could also modify its carcinogenicity.

  11. Controlled synthesis of N,N,N-trimethyl chitosan for modulated bioadhesion and nasal membrane permeability.

    PubMed

    Pardeshi, Chandrakantsing V; Belgamwar, Veena S

    2016-01-01

    In an experiment to explore the bioadhesion, biocompatibility, and membrane permeation properties, the controlled synthesis of N,N,N-trimethyl chitosan (TMC) was carried out by two-step reductive methylation of chitosan (CHT). Methylation was confirmed by (1)H NMR (δ=3.1 ppm) and FTIR analysis (CH stretch at 1,485 cm(-1)). The TMC was further characterized by DSC, TGA, XRD, HR-TEM, SEM, and elemental analysis. Findings revealed improved solubility, enhanced viscosity, increased swelling index and higher molecular weight of TMC over CHT. Comparative evaluation validated increased bioadhesion potential, and improved ex vivo biocompatibility of TMC compared to CHT. Increased bioadhesion of TMC NPs over CHT NPs can be attributed to the strong electrostatic interactions between cationic amino groups with anionic sialic and sulfonic acid moieties contained in the mucin of the nasal mucus. Ex vivo biocompatibility studies suggested that the NP formulations of both biopolymers were biocompatible and could be applied safely on the nasal epithelium. Ex vivo permeation studies executed on excised cattle nasal mucosa illustrated improved permeability of TMC NPs over CHT NPs. In the author's opinion, two-step reductive methylation of CHT could be an attractive strategy to improve its solubility, bioadhesion, and permeation characteristics without affecting biocompatibility across the mucosal surfaces.

  12. PMMA-N,N,N-trimethyl chitosan nanoparticles for fabrication of antibacterial natural rubber latex gloves.

    PubMed

    Arpornwichanop, Thanida; Polpanich, Duangporn; Thiramanas, Raweewan; Suteewong, Teeraporn; Tangboriboonrat, Pramuan

    2014-08-30

    This paper presents one-pot synthesis of N,N,N-trimethyl chitosan (TMC) stabilized poly(methyl methacrylate) (PMMA) latex particles via the miniemulsion polymerization technique. From (1)H NMR, synthesized TMC contains 52% degree of quaternization. Compared to native biopolymer chitosan, TMC possesses permanently positive charges as well as provides greater antibacterial activity. Combining properties of PMMA and TMC, PMMA-TMC latex nanoparticles (hydrodynamic size ≈282 nm) could be used in place of inorganic lubricating powder in fabrication of latex gloves at pH ≥ 7. After immersing sulphur prevulcanized natural rubber (SPNR) film into 3 wt% of PMMA-TMC latex at pH 7, significant amount of nanoparticles uniformly deposited onto SPNR film was observed under SEM. A number of nanoparticles present on film surface would increase surface roughness of the rubber film and potentially inhibit the bacterial (Escherichia coli and Staphylococcus aureus) growth, which would be useful for fabrication of special gloves with antibacterial property.

  13. Systemic modulation by ultraviolet irradiation of cutaneous N-methyl-N'-nitro-N-nitrosoguanidine-induced carcinogenesis.

    PubMed

    Gensler, H L

    1992-01-10

    Ultraviolet irradiation can systemically enhance subsequent skin cancer induction by benzo[a]pyrene, methylcholanthrene, or UV radiation. The present study was designed to determine whether UVB irradiation influences host susceptibility to the alkylating agent N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). Female C3H/HeJ mice were exposed dorsally to UVB radiation from banks of 6 Westinghouse FS40 sun lamps. The mice received a total UV dose of approximately 8.1 x 10(5) J m-2 over a 15-week period. After termination of UVB treatments, ventral tumors were induced by 4 applications of 30 mumol of MNNG at 8-day intervals. At 20 weeks after the first MNNG treatment, UVB-irradiated mice had 7-fold more MNNG-induced, ventral tumors than did the unirradiated control mice (P = 0.026, Wilcoxon rank sum test). Ventral application of MNNG after cessation of dorsal UVB exposure, but before UV tumor appearance, did not influence photocarcinogenesis. These results demonstrate that UV irradiation can systemically decrease host resistance to tumor induction by the methylating agent, MNNG.

  14. Reactive Resonances in N+N2 Exchange Reaction

    NASA Technical Reports Server (NTRS)

    Wang, Dunyou; Huo, Winifred M.; Dateo, Christopher E.; Schwenke, David W.; Stallcop, James R.

    2003-01-01

    Rich reactive resonances are found in a 3D quantum dynamics study of the N + N2 exchange reaction using a recently developed ab initio potential energy surface. This surface is characterized by a feature in the interaction region called Lake Eyring , that is, two symmetric transition states with a shallow minimum between them. An L2 analysis of the quasibound states associated with the shallow minimum confirms that the quasibound states associated with oscillations in all three degrees of freedom in Lake Eyring are responsible for the reactive resonances in the state-to-state reaction probabilities. The quasibound states, mostly the bending motions, give rise to strong reasonance peaks, whereas other motions contribute to the bumps and shoulders in the resonance structure. The initial state reaction probability further proves that the bending motions are the dominating factors of the reaction probability and have longer life times than the stretching motions. This is the first observation of reactive resonances from a "Lake Eyring" feature in a potential energy surface.

  15. AlGaN/InGaN Photocathode Development

    SciTech Connect

    Buckley, J. H.; Leopold, D. J.

    2008-12-24

    An increase in quantum efficiency in photodetectors could result in a proportional reduction in the area of atmospheric Cherenkov telescopes and an even larger reduction in cost. We report on the development of high quantum efficiency, high gain, UV/blue photon-counting detectors based on AlGaN/InGaN photocathode heterostructures grown by molecular beam epitaxy. This research could eventually result in nearly ideal light detectors with a number of distinct advantages over existing technologies for numerous applications in high-energy physics and particle astrophysics. Potential advantages include much lower noise detection, better stability and radiation resistance than other cathode structures, high VUV sensitivity and very low radioactive background levels for deep underground experiments, and high detection efficiency for the detection of individual VUV-visible photons. We are also developing photocathodes with intrinsic gain, initially improving the detection efficiency of hybrid semiconductor-vacuum tube devices and eventually leading to a new type of all-solid-state photomultiplier device.

  16. Quantifying N2O reduction to N2 based on N2O isotopocules - validation with independent methods (helium incubation and 15N gas flux method)

    NASA Astrophysics Data System (ADS)

    Lewicka-Szczebak, Dominika; Augustin, Jürgen; Giesemann, Anette; Well, Reinhard

    2017-02-01

    Stable isotopic analyses of soil-emitted N2O (δ15Nbulk, δ18O and δ15Nsp = 15N site preference within the linear N2O molecule) may help to quantify N2O reduction to N2, an important but rarely quantified process in the soil nitrogen cycle. The N2O residual fraction (remaining unreduced N2O, rN2O) can be theoretically calculated from the measured isotopic enrichment of the residual N2O. However, various N2O-producing pathways may also influence the N2O isotopic signatures, and hence complicate the application of this isotopic fractionation approach. Here this approach was tested based on laboratory soil incubations with two different soil types, applying two reference methods for quantification of rN2O: helium incubation with direct measurement of N2 flux and the 15N gas flux method. This allowed a comparison of the measured rN2O values with the ones calculated based on isotopic enrichment of residual N2O. The results indicate that the performance of the N2O isotopic fractionation approach is related to the accompanying N2O and N2 source processes and the most critical is the determination of the initial isotopic signature of N2O before reduction (δ0). We show that δ0 can be well determined experimentally if stable in time and then successfully applied for determination of rN2O based on δ15Nsp values. Much more problematic to deal with are temporal changes of δ0 values leading to failure of the approach based on δ15Nsp values only. For this case, we propose here a dual N2O isotopocule mapping approach, where calculations are based on the relation between δ18O and δ15Nsp values. This allows for the simultaneous estimation of the N2O-producing pathways' contribution and the rN2O value.

  17. [Effects of urease/nitrification inhibitors on soil available N and microbial biomass N and on N uptake of wheat].

    PubMed

    Jiao, Xiaoguang; Liang, Wenju; Chen, Lijun; Jiang, Yong; Wen, Dazhong

    2004-10-01

    With an aquic brown earth as test soil, this paper studied the effects of urease inhibitor (NBPT), nitrification inhibitor (DCD) and their combinations on the dynamics of soil available N and microbial biomass N. The results showed that the treatments of inhibitors, especially the combined application of NBPT and DCD, could increase soil NH4+-N by 2%-53%, inhibit NH4+ oxidation, decrease soil NO3(-)-N concentration, increase soil total available N by 34%-44%, and increase wheat N uptake by 0.26%-6.79%. The best treatment was urease inhibitor combined with nitrification inhibitor. The application of inhibitors increased soil microbial biomass N immobilization at the early growth stage of wheat, and promoted soil N mineralization at filling stage.

  18. N(7)-protonation-induced conformational flipping in hypermodified nucleic acid base N 6-(N-glycylcarbonyl) adenine

    NASA Astrophysics Data System (ADS)

    Tewari, Ravindra

    1995-06-01

    Protonation-induced conformational changes are studied in the hypermodified nucleic acid base N 6-(N-glycylcarbonyl) adenine, gc 6Ade, using the quantum chemical perturbative configuration interaction using localised orbitals method. Protonation at the N(7) position of adenine in gc 6Ade induces reorientation of the N 6 substituent, so as to allow stabilisation through an intramolecular hydrogen bond involving N(7)H and the carbonyl oxygen in the glycylcarbonyl substituent. The relative orientation of the carboxyl group with respect to the carbonyl group in the ureido HNCONH linkage is predicted to be similar to that in unprotonated gc 6Ade. The theoretically preferred proximal conformation of N(7)-protonated gc 6Ade restores the participation of N(6)H and N(1) in the Watson-Crick base pairing similar to that in unmodified adenine. This unique orientation can be significant for altering the reading frame in codon-anticodon interactions.

  19. Tests of N-85, N-86 and N-87 airfoil sections in the 11-inch high speed wind tunnel

    NASA Technical Reports Server (NTRS)

    Stack, John; Lindsey, W F

    1938-01-01

    Three airfoils, the N-85, the N-86, and the N-87, were tested at the request of the Bureau of Aeronautics, Navy Department, to determine the suitability of these sections for use as propeller-blade sections. Further tests of the NACA 0009-64 airfoil were also made to measure the aerodynamic effect of thickening the trailing edge in accordance with current propeller practice. The N-86 and the N-87 airfoils appear to be nearly equivalent aerodynamically and both are superior to the N-85 airfoil. Comparison of those airfoils with the previously developed NACA 2409-34 airfoils indicate that the NACA 2409-34 is superior, particularly at high speeds. Thickening the trailing edge appears to have a detrimental effect, although the effect may be small if the trailing-edge radius is less than 0.5 percent of the cord. The N-86 and the N-87 airfoils appear to be nearly equivalent.

  20. Physics of gate leakage current in N-polar InAlN/GaN heterojunction field effect transistors

    SciTech Connect

    Goswami, Arunesh; Trew, Robert J.; Bilbro, Griff L.

    2014-10-28

    A physics based model of the gate leakage current in N-polar InAlN/GaN heterojunction field effect transistors is demonstrated. The model is based on the space charge limited current flow dominated by the effects of deep traps in the InAlN surface layer. The model predicts accurately the gate-leakage measurement data of the N-polar InAlN/GaN device with InAlN cap layer. In the pinch-off state, the gate leakage current conduction through the surface of the device in the drain access region dominates the current flow through the two dimensional electron gas channel. One deep trap level and two levels of shallow traps are extracted by fitting the model results with measurement data.

  1. Step-flow growth mode instability of N-polar GaN under N-excess

    SciTech Connect

    Chèze, C.

    2013-08-12

    GaN layers were grown on N-polar GaN substrates by plasma-assisted molecular beam epitaxy under different III/V ratios. Ga-rich conditions assure step-flow growth with atomically flat surface covered by doubly-bunched steps, as for Ga-polar GaN. Growth under N-excess however leads to an unstable step-flow morphology. Particularly, for substrates slightly miscut towards <1010>, interlacing fingers are covered by atomic steps pinned on both sides by small hexagonal pits. In contrast, a three-dimensional island morphology is observed on the Ga-polar equivalent sample. We attribute this result to lower diffusion barriers on N-polar compared to Ga-polar GaN under N-rich conditions.

  2. Bulk ammonothermal GaN

    NASA Astrophysics Data System (ADS)

    Dwiliński, R.; Doradziński, R.; Garczyński, J.; Sierzputowski, L. P.; Puchalski, A.; Kanbara, Y.; Yagi, K.; Minakuchi, H.; Hayashi, H.

    2009-05-01

    In this work, results of structural characterization of high-quality ammonothermal GaN are presented. Besides expected low dislocation density (being of the order of 10 3 cm -2) the most interesting feature seems perfect flatness of the crystal lattice of studied crystals. Regardless the size of crystals, lattice curvature radius exceeds 100 m, whereas better crystals reveal radius of several hundred meters and the best above 1000 m. Excellent crystallinity manifests in very narrow X-ray diffraction peaks of full-width at half-maximum (FWHM) values about 16 arcsec.

  3. Clasificación orbital

    NASA Astrophysics Data System (ADS)

    Carpintero, D. D.; Aguilar, L. A.

    Presentamos un método para clasificar órbitas generales en potenciales de 2 y 3 dimensiones, basado en el concepto de dinámica espectral introducido por Binney y Spergel (ApJ 252, 308, 1982). Este método distingue correctamente órbitas regulares e irregulares, familias de órbitas (cajas, tubos, etc.), y resonancias, aún cuando son de alto orden o de rango mayor que 1. Se propone asimismo una nueva nomenclatura para la clasificación de órbitas.

  4. N2H+ and N15NH+ toward the prestellar core 16293E in L1689N

    NASA Astrophysics Data System (ADS)

    Daniel, F.; Faure, A.; Pagani, L.; Lique, F.; Gérin, M.; Lis, D.; Hily-Blant, P.; Bacmann, A.; Roueff, E.

    2016-07-01

    Context. Understanding the processes that could lead to an enrichment of molecules in 15N atoms is of particular interest because this may shed light on the relatively strong variations observed in the 14N/15N ratio in various solar system environments. Aims: The sample of molecular clouds where 14N/15N ratios have been measured currently is small and has to be enlarged to allow statistically significant studies. In particular, the N2H+ molecule currently shows the broadest spread of 14N/15N ratios in high-mass star-forming regions. However, the 14N/15N ratio in N2H+ was obtained in only two low-mass star-forming regions (L1544 and B1b). We here extend this sample to a third dark cloud. Methods: We targeted the 16293E prestellar core, where the N15NH+J = 1-0 line was detected. Using a model previously developed for the physical structure of the source, we solved the molecular excitation with a nonlocal radiative transfer code. For this purpose, we computed specific collisional rate coefficients for the N15NH+-H2 collisional system. As a first step of the analysis, the N2H+ abundance profile was constrained by reproducing the N2H+J = 1-0 and 3-2 maps. A scaling factor was then applied to this profile to match the N15NH+J = 1-0 spectrum. Results: We derive a column density ratio N2H+/N15NH. Conclusions: We performed a detailed analysis of the excitation of N2H+ and N15NH+ in the direction of the 16293E core with modern models that solve the radiative transfer and with the most accurate collisional rate coefficients available to date. We obtained the third estimate of the N2H+/N15NH+ column density ratio in the direction of a cold prestellar core. The current estimate ~330 agrees with the typical value of the elemental isotopic ratio in the local interstellar medium. It is lower than in some other cores, however, where values as high as 1300 have been reported.

  5. Climate-Dependence of Plant-Soil 15N/14N Interactions Across Tropical Rainforests

    NASA Astrophysics Data System (ADS)

    Houlton, B. Z.; Sigman, D. M.; Hedin, L. O.

    2005-12-01

    In most areas of the world, the 15N/14N of bulk soils is higher than that of plant leaves, and the isotopic signatures of these two ecosystem N pools progressively diverge with increasing rainfall. However, both the cause for this isotopic trend and its implications for understanding interactions between climate and N cycles are largely unknown. We report 15N/14N measurements of nitrate, ammonium, and total dissolved N in soil extracts from a highly constrained rainfall sequence in Hawaii, across which this trend in ecosystem 15N/14N is captured, to examine the competing explanations for plant-soil 15N/14N uncouplings. While the isotopic influences of microbial transfers of N between nitrate and ammonium pools and plant-mycorrhizae interactions have been posited in plant-soil 15N/14N relationships, our data did not support an important role for either of these mechanisms. Instead, preferential regeneration of 14N during the breakdown of DON to ammonium explains why the 15N/14N of plants is lower than that of bulk soils. Fractionation at this step leads to two isotopically distinct N subcycles in each forest, a lower-15N/14N subcycle composed of ammonium, nitrate, and bulk plant biomass N that `spins' rapidly and a higher-15N/14N subcycle composed of bulk soil N and DON that is much less dynamic. The increased difference between soil and plant 15N/14N is due to changes in the impacts of nitrification and denitrification on the 15N/14N of ammonium and nitrate, coupled with a switch from nitrate to ammonium uptake by plants under the wettest conditions. For instance, the particularly large (~6 per mil) 15N/14N difference between plants and soils in the wettest sites is due to the lack of 15N-enrichment of ammonium by nitrification coupled with plant dependence on ammonium uptake only. Our results highlight the importance of interactions between DON breakdown, ecosystem N recycling, and gaseous N losses in the explaining the interactions between the 15N signatures of

  6. Dynamical coupled-channels study of {pi}N {right arrow} {pi pi}N reactions.

    SciTech Connect

    Kamano, H.; Julia-Diaz, B.; Lee, T.-S. H.; Matsuyama, A.; Sato, T.; Physics; Jefferson Lab.; Univ. of Barcelona; Shizuoka Univ.; Osaka Univ.

    2009-02-24

    As a step toward performing a complete coupled-channels analysis of the world data of {pi}N,{gamma}*N {yields} {pi}N,{eta}N,{pi}{pi}N reactions, the {pi}N {yields} {pi}{pi}N reactions are investigated starting with the dynamical coupled-channels model developed in Phys. Rev. C 76, 065201 (2007). The channels included are {pi}N,{eta}N, and {pi}{pi}N which has {pi}{Delta},{rho}N, and {sigma}N resonant components. The nonresonant amplitudes are generated from solving a set of coupled-channels equations with the meson-baryon potentials defined by effective Lagrangians. The resonant amplitudes are generated from 16 bare excited nucleon (N*) states that are dressed by the nonresonant interactions as constrained by the unitarity condition. The data of total cross sections and {pi}N and {pi}{pi} invariant mass distributions of {pi} + p {yields} {pi} + {pi} + n, {pi} + {pi}0p and {pi} - p {yields} {pi} + {pi} - n, {pi} - {pi}0p,{pi}0{pi}0n reactions from threshold to the invariant mass W = 2 GeV can be described to a very large extent. We show the importance of the coupled-channels effects and the strong interference among the contributions from the {pi}{Delta},{sigma}N, and {rho}N channels. The large interference between the resonant and nonresonant amplitudes is also demonstrated. Possible future developments are discussed.

  7. Energy relaxation of hot electrons in lattice-matched AlInN/AlN/GaN heterostructures

    SciTech Connect

    Zhang, J.-Z.; Dyson, A.; Ridley, B. K.

    2013-12-04

    Using the dielectric continuum model, hot-electron power dissipation and energy relaxation times are calculated for a typical lattice-matched AlInN/AlN/GaN heterostructure, including effects of hot phonons and screening from the mobile electrons. The calculated power dissipation and energy relaxation times are very close to the experimental data.

  8. 15N Abundance of Nodules as an Indicator of N Metabolism in N2-Fixing Plants 1

    PubMed Central

    Shearer, Georgia; Feldman, Lori; Bryan, Barbara A.; Skeeters, Jerri L.; Kohl, Daniel H.; Amarger, Nöelle; Mariotti, Françoise; Mariotti, André

    1982-01-01

    This paper expands upon previous reports of 15N elevation in nodules (compared to other tissues) of N2-fixing plants. N2-Fixing nodules of Glycine max (soybeans), Vigna unguiculata (cowpea), Phaseolus vulgaris (common bean), Phaseolus coccineus (scarlet runner bean), Prosopis glandulosa (mesquite), and Olneya tesota (desert ironwood) were enriched in 15N. Nodules of Vicia faba (fava beans), Arachis hypogaea (peanut), Trifolium pratense (red clover), Pisum sativum (pea), Lathyrus sativus (grass pea), Medicago sativa (alfalfa), and Lupinus mutabilis (South American lupine) were not; nor were the nodules of nine species of N2-fixing nonlegumes. The nitrogen of ineffective nodules of soybeans and cowpeas was not enriched in 15N. Thus, 15N elevation in nodules of these plants depends on active N2-fixation. Results obtained so far on the generality of 15N enrichment in N2-fixing nodules suggest that only the nodules of plants which actively fix N2 and which transport allantoin or allantoic acid exhibit 15N enrichment. PMID:16662517

  9. Large-N solution of the heterotic N=(0,1) two-dimensional O(N) sigma model

    SciTech Connect

    Koroteev, Peter; Monin, Alexander

    2010-05-15

    In this paper we build a family of heterotic deformations of the O(N) sigma model. These deformations break (1,1) supersymmetry down to (0,1) symmetry. We solve this model at large N. We also find an alternative superfield formulation of the heterotic CP{sup N} sigma model, which was discussed in the literature before.

  10. Optical spectra of protected diamine 10-bond-bridged intervalence radical cations related to N,N,N'N'-tetraalkylbenzidine.

    PubMed

    Nelsen, Stephen F; Luo, Yun; Weaver, Michael N; Lockard, Jenny V; Zink, Jeffrey I

    2006-05-26

    The optical absorption spectra of the delocalized intervalence radical cations of seven o,o'-linked benzidine derivatives that have the nitrogens protected as 9-(9-aza-bicyclo[3.3.1]nonan-3-one) derivatives are discussed and compared with that of the p-phenylene radical cation. The linking units are CH2, CH2CH2, NMe, S, SO2, and C=O, and we also studied H,H (the unlinked benzidine). The lowest-energy absorption band is assigned as the transition from the antibonding combination of symmetrical N and aromatic orbitals to the antibonding combination of the antisymmetric N and aromatic orbitals using TD-DFT calculations, and a good correlation between the observed transition energies and those calculated using the simple Koopmans theorem-based "neutral in-cation geometry" calculations on the UB3LYP/6-31G* structures is found. The use of the two-state model that equates the electronic interaction through the bridge between the amino groups with half of the lowest transition energy is seriously incorrect for these and other delocalized intervalence compounds. The problem of extracting the electronic interactions that actually are involved from calculated transition energies is discussed.

  11. Disorder in large- N theories

    NASA Astrophysics Data System (ADS)

    Aharony, Ofer; Komargodski, Zohar; Yankielowicz, Shimon

    2016-04-01

    We consider Euclidean Conformal Field Theories perturbed by quenched disorder, namely by random fluctuations in their couplings. Such theories are relevant for second-order phase transitions in the presence of impurities or other forms of disorder. Theories with quenched disorder often flow to new fixed points of the renormalization group. We begin with disorder in free field theories. Imry and Ma showed that disordered free fields can only exist for d > 4. For d > 4 we show that disorder leads to new fixed points which are not scale-invariant. We then move on to large- N theories (vector models or gauge theories in the `t Hooft limit). We compute exactly the beta function for the disorder, and the correlation functions of the disordered theory. We generalize the results of Imry and Ma by showing that such disordered theories exist only when disorder couples to operators of dimension Δ > d/4. Sometimes the disordered fixed points are not scale-invariant, and in other cases they have unconventional dependence on the disorder, including non-trivial effects due to irrelevant operators. Holography maps disorder in conformal theories to stochastic differential equations in a higher dimensional space. We use this dictionary to reproduce our field theory results. We also study the leading 1 /N corrections, both by field theory methods and by holography. These corrections are particularly important when disorder scales with the number of degrees of freedom.

  12. WH(n) under pressure.

    PubMed

    Zaleski-Ejgierd, Patryk; Labet, Vanessa; Strobel, Timothy A; Hoffmann, Roald; Ashcroft, N W

    2012-04-18

    An initial observation of the formation of WH under pressure from W gaskets surrounding hydrogen in diamond anvil cells led to a theoretical study of tungsten hydride phases. At P = 1 atm no stoichiometry is found to be stable with respect to separation into the elements, but as the pressure is raised WH(n) (n = 1-6, 8) stoichiometries are metastable or stable. WH and WH(4) are calculated to be stable at P > 15 GPa, WH(2) becomes stable at P > 100 GPa and WH(6) at P > 150 GPa. In agreement with experiment, the structure computed for WH is anti-NiAs. WH(2) shares with WH a hexagonal arrangement of tungsten atoms, with hydrogen atoms occupying octahedral and tetrahedral holes. For WH(4) the W atoms are in a distorted fcc arrangement. As the number of hydrogens rises, the coordination of W by H increases correspondingly, leading to a twelve-coordinated W in WH(6). In WH(8) H(2) units also develop. All of the hydrides considered should be metallic at high pressure, though the Fermi levels of WH(4) and WH(6) lie in a deep pseudogap. Prodded by these theoretical studies, experiments were then undertaken to seek phases other than WH, exploring a variety of experimental conditions that would favor further reaction. Though a better preparation and characterization of WH resulted, no higher hydrides have as yet been found.

  13. Twisting the N=2 string

    NASA Astrophysics Data System (ADS)

    Ketov, Sergei V.; Lechtenfeld, Olaf; Parkes, Andrew J.

    1995-03-01

    The most general homogeneous monodromy conditions in N=2 string theory are classified in terms of the conjugacy classes of the global symmetry group U(1,1)⊗openZ2. For classes which generate a discrete subgroup Γ, the corresponding target space backgrounds openC1,1/Γ include half spaces, complex orbifolds, and tori. We propose a generalization of the intercept formula to matrix-valued twists, but find massless physical states only for Γ=open1 (untwisted) and Γ=openZ2 (in the manner of Mathur and Mukhi), as well as for Γ being a parabolic element of U(1,1). In particular, the 16 openZ2-twisted sectors of the N=2 string are investigated, and the corresponding ground states are identified via bosonization and BRST cohomology. We find enough room for an extended multiplet of ``spacetime'' supersymmetry, with the number of supersymmetries being dependent on global ``spacetime'' topology. However, world-sheet locality for the chiral vertex operators does not permit interactions among all massless ``spacetime'' fermions.

  14. Coating MCPs with AlN and GaN

    NASA Technical Reports Server (NTRS)

    Bensaoula, Abdelhakim; Starikov, David; Boney, Chris

    2006-01-01

    A development effort underway at the time of reporting the information for this article is devoted to increasing the sensitivity of microchannel plates (MCPs) as detectors of photons and ions by coating the MCPs with nitrides of elements in period III of the periodic table. Conventional MCPs are relatively insensitive to slowly moving, large-mass ions for example, ions of biomolecules under analysis in mass spectrometers. The idea underlying this development is to coat an MCP to reduce its work function (decrease its electron affinity) in order to increase both (1) the emission of electrons in response to impingement of low-energy, large-mass ions and (2) the multiplying effect of secondary electron emission. Of particular interest as coating materials having appropriately low or even negative electron affinities are gallium nitride, aluminum nitride, and ternary alloys of general composition Al(x)Ga(1-x)N (where 0N and GaN both undoped and doped with Si were deposited on commercial MCPs by radio-frequency molecular-beam epitaxy (also known as plasma-assisted molecular-beam epitaxy) at temperatures <200 C. This deposition technique is particularly suitable because (1) MCPs cannot withstand the higher deposition-substrate temperatures used to decompose constituent compounds in some other deposition techniques and (2) in this technique, the constituent Al, Ga, and N

  15. 40 CFR 721.10173 - Silanamine,1,1,1-triethoxy-N,N-diethyl-.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Silanamine,1,1,1-triethoxy-N,N-diethyl... Specific Chemical Substances § 721.10173 Silanamine,1,1,1-triethoxy-N,N-diethyl-. (a) Chemical substance...,1-triethoxy-N,N-diethyl- (PMN P-03-793; CAS No. 35077-00-0) is subject to reporting under...

  16. 40 CFR 721.10173 - Silanamine,1,1,1-triethoxy-N,N-diethyl-.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Silanamine,1,1,1-triethoxy-N,N-diethyl... Specific Chemical Substances § 721.10173 Silanamine,1,1,1-triethoxy-N,N-diethyl-. (a) Chemical substance...,1-triethoxy-N,N-diethyl- (PMN P-03-793; CAS No. 35077-00-0) is subject to reporting under...

  17. 40 CFR 721.10173 - Silanamine,1,1,1-triethoxy-N,N-diethyl-.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Silanamine,1,1,1-triethoxy-N,N-diethyl... Specific Chemical Substances § 721.10173 Silanamine,1,1,1-triethoxy-N,N-diethyl-. (a) Chemical substance...,1-triethoxy-N,N-diethyl- (PMN P-03-793; CAS No. 35077-00-0) is subject to reporting under...

  18. 40 CFR 721.10173 - Silanamine,1,1,1-triethoxy-N,N-diethyl-.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Silanamine,1,1,1-triethoxy-N,N-diethyl... Specific Chemical Substances § 721.10173 Silanamine,1,1,1-triethoxy-N,N-diethyl-. (a) Chemical substance...,1-triethoxy-N,N-diethyl- (PMN P-03-793; CAS No. 35077-00-0) is subject to reporting under...

  19. Asymmetric Induction by a Nitrogen (14) N/(15) N Isotopomer in Conjunction with Asymmetric Autocatalysis.

    PubMed

    Matsumoto, Arimasa; Ozaki, Hanae; Harada, Shunya; Tada, Kyohei; Ayugase, Tomohiro; Ozawa, Hitomi; Kawasaki, Tsuneomi; Soai, Kenso

    2016-12-05

    Chirality arising from isotope substitution, especially with atoms heavier than the hydrogen isotopes, is usually not considered a source of chirality in a chemical reaction. An N(2) ,N(2) ,N(3) ,N(3) -tetramethyl-2,3-butanediamine containing nitrogen ((14) N/(15) N) isotope chirality was synthesized and it was revealed that this isotopically chiral diamine compound acts as a chiral initiator for asymmetric autocatalysis.

  20. Growth in the global N2 sink attributed to N fertilizer inputs over 1860 to 2000.

    PubMed

    Wang, Chao; Houlton, Benjamin Z; Dai, Weiwei; Bai, Edith

    2017-01-01

    Cropland expansion and fertilizer applications are among the most important substantial effects of human actions on the global nitrogen (N) cycle. However, questions remain over the fate of anthropogenic N inputs, particularly whether a significant fraction of N-based fertilizers have been lost to inert N2 or reactive N forms. Here, we combine natural N isotope constraints on the pre-industrial N cycle with global mass-balance modeling to investigate the role of cropland conversion on gaseous N emissions and hydrological N leaching fluxes. We estimate that cropland expansion has been accompanied by >9-fold increase in N input rates to cropping systems, roughly doubling the baseline N budget of the terrestrial biosphere. As a consequence, approximately 10 times more N is exported from modern croplands to the hydrosphere than in 1860, with a five-fold increase in cropland N gases emission to the atmosphere. Atmospheric NH3, NO, N2O and N2 fluxes increased from 8.6, 16.6, 11.7 and 31.9TgNyr(-1), respectively, in 1860 to 17.7, 23.6, 15.2 and 39.7TgNyr(-1), respectively, by 2000. Thus, the growth in N2 accounted for ~20% of cropland-driven N losses (dissolved plus gaseous pathways), with the remaining 80% exported as reactive N forms. Although the increase in N2 emissions has mitigated some of the unwanted side-effects of N fertilizer applications on human health, the economy, and climate change, this inert sink has been unable to keep pace with the increase in N inputs for enhanced food production. Our results imply that, unless new management steps are taken, an increasing fraction of N fertilizers will mobilize to reactive N forms in the global land, air and water systems, thus further accelerating the negative consequences of human modifications of the N cycle this century.

  1. Asymmetric Induction by a Nitrogen 14N/15N Isotopomer in Conjunction with Asymmetric Autocatalysis

    PubMed Central

    Ozaki, Hanae; Harada, Shunya; Tada, Kyohei; Ayugase, Tomohiro; Ozawa, Hitomi; Kawasaki, Tsuneomi

    2016-01-01

    Abstract Chirality arising from isotope substitution, especially with atoms heavier than the hydrogen isotopes, is usually not considered a source of chirality in a chemical reaction. An N 2 ,N 2 ,N 3 ,N 3‐tetramethyl‐2,3‐butanediamine containing nitrogen (14N/15N) isotope chirality was synthesized and it was revealed that this isotopically chiral diamine compound acts as a chiral initiator for asymmetric autocatalysis. PMID:27754589

  2. Octanol-water partition coefficients of substituted alpha, N-diphenylnitrones and benzonitrile N-oxides

    SciTech Connect

    Kirchner, J.J.; Acree, W.E. Jr.; Leo, A.J.; Gelli, G.

    1985-10-01

    Experimental octanol-water partition coefficients are reported for substituted alpha, N-diphenylnitrones and benzonitrile N-oxides. The results of these measurements are used to calculate the aromatic fragment constants pi HC = N(O)C6H5, pi C = N----O, fHC = N(O), and fC = N----O for the group contribution methods of Hansch and Leo.

  3. Terahertz-frequency InN/GaN heterostructure-barrier varactor diodes.

    PubMed

    Reklaitis, A

    2008-09-24

    Frequency multipliers based on the single-barrier and double-barrier InN/GaN heterostructure varactor diodes are suggested. The DC and large-signal AC vertical electron transport in the InN/GaN diodes are investigated by ensemble Monte Carlo simulations. It is found that InN/GaN heterostructure-barrier varactor diodes are able to operate as efficient frequency multipliers in the frequency range up to 1 THz.

  4. Terahertz-frequency InN/GaN heterostructure-barrier varactor diodes

    NASA Astrophysics Data System (ADS)

    Reklaitis, A.

    2008-09-01

    Frequency multipliers based on the single-barrier and double-barrier InN/GaN heterostructure varactor diodes are suggested. The DC and large-signal AC vertical electron transport in the InN/GaN diodes are investigated by ensemble Monte Carlo simulations. It is found that InN/GaN heterostructure-barrier varactor diodes are able to operate as efficient frequency multipliers in the frequency range up to 1 THz.

  5. 40 CFR 721.10173 - Silanamine,1,1,1-triethoxy-N,N-diethyl-.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Silanamine,1,1,1-triethoxy-N,N-diethyl... Specific Chemical Substances § 721.10173 Silanamine,1,1,1-triethoxy-N,N-diethyl-. (a) Chemical substance...,1-triethoxy-N,N-diethyl- (PMN P-03-793; CAS No. 35077-00-0) is subject to reporting under...

  6. Discriminative Stimulus Effects of N,N-Diisopropyltryptamine

    PubMed Central

    Carbonaro, Theresa M.; Forster, Michael J.; Gatch, Michael B.

    2012-01-01

    Rationale Serotonergic hallucinogens such as (+)-lysergic acid diethylamide (LSD) and dimethyltryptamine (DMT) produce distinctive visual effects, whereas the synthetic hallucinogen N,N-diisopropyltryptamine (DiPT) is known for its production of auditory distortions. Objective: This study compares the discriminative stimulus effects of DiPT to those of visual hallucinogens. Methods Adult male rats were trained to discriminate DiPT (5 mg/kg, 15 min) from saline under a FR10 schedule. A dose-effect and time course of DiPT’s discriminative stimulus effects were established. DMT, (−)-2,5-dimethoxy-4-methylamphetamine (DOM), LSD, (±)-methylenedioxymethamphetamine (MDMA) and (+)-methamphetamine were tested for cross-substitution in DiPT-trained animals. Results Rats learned to discriminate DiPT from saline in an average of 60 training sessions (30 drug and 30 saline). DiPT (0.5 – 5 mg/kg) produced dose-dependent increases in drug-appropriate responding (DAR) to 99% (ED50 = 2.47 mg/kg). Onset of the discriminative stimulus effects was within 5 minutes and the effects dissipated within 4 hours. Full substitution for the discriminative stimulus effects of DiPT occurred with LSD, DOM and MDMA. DMT only partially substituted for DiPT (65% DAR), whereas (+)-methamphetamine failed to substitute for DiPT (29% DAR). Conclusions The discriminative stimulus effects of DiPT were similar those of a number of synthetic hallucinogens, only partially similar to those of DMT, but not similar to (+)-methamphetamine. The putative DiPT-induced auditory distortions do not lead to discriminative stimulus effects distinguishable from other hallucinogens. PMID:23070023

  7. H3N2v and You

    MedlinePlus

    ... Influenza A (H3N2)v in Health Care Settings Interim Information for Clinicians about Human Infections with H3N2v Virus Interim Guidance for Enhanced Influenza Surveillance: Additional Specimen Collection ...

  8. Cone Penetrometer N Factor Determination Testing Results

    SciTech Connect

    Follett, Jordan R.

    2014-03-05

    This document contains the results of testing activities to determine the empirical 'N Factor' for the cone penetrometer in kaolin clay simulant. The N Factor is used to releate resistance measurements taken with the cone penetrometer to shear strength.

  9. Sylvanus Albert Reed Award: Eastman N. Jacobs

    NASA Technical Reports Server (NTRS)

    1937-01-01

    Sylvanus Albert Reed Award - Eastman N. Jacobs: In 1937, Eastman N. Jacobs, one of Langley's most adventurous researchers, received the Sylvanus Albert Reed Award for his contributions to the aerodynamic improvement of airfoils.

  10. A high-performance liquid chromatography method for determination 2-(n-(N,N,N-trimethyl)-n-alkyl)-5-alkylfuryl halides in dipalmitoylphosphatidilcholine liposome solutions.

    PubMed

    Morales, Javier; Zanocco, Antonio L; Günther, Germán; Lemp, Else

    2006-08-25

    A high-performance liquid chromatography (HPLC) method for the determination of 2-(4-(N,N,N-trimethyl)-butyl)-5-dodecylfuryl bromide (DFTA) in dipalmitoylphophatidil-choline (DPPC) liposome solutions has been developed. Lipid-soluble furan derivatives, 2,5-disubstituted with different n-alkyl chains and a terminal trimethylammonium group are useful probes for studying singlet oxygen dynamics and equilibria in microcompartmentalized systems. The actual HPLC method uses a gradient elution and DAD detection. The chromatographic separation of these components is achieved using a C18 analytical column with a 10mM solution of 1-heptanesulfonic acid (PIC-7)-methanol (10:90, v/v) as initial mobile phase. Both DFTA peaks are well resolved and free of interference from matrix components and reaction products. The method has been found to be linear (r > 0.999) over a wide concentration range and reliable to perform kinetic experiments in which the time dependent consumption of a tetraalkylammonium surfactant in a microorganized systems composed by lipidic surfactants is followed.

  11. GaN and AlGaN/GaN heterostructures grown on two dimensional BN templates

    NASA Astrophysics Data System (ADS)

    Snure, Michael; Siegel, Gene; Look, David C.; Paduano, Qing

    2017-04-01

    Two dimension materials, like BN and graphene, have been shown to be excellent templates for the growth and fabrication of freestanding III-nitride materials. In this paper we study the effects of BN morphology on GaN and AlGaN/GaN heterostructures grown on these templates. The crystallinity, transport, and optical properties of the GaN layer are examined and found to be well correlated to the BN template. The self-separation of GaN from the BN/sapphire template is also connected to morphology, resulting in freestanding GaN layers. Transport properties of Si doped GaN and AlGaN/GaN heterostructures were examined for different BN templates. The bulk GaN mobility was closely linked to the morphology of the BN template resulting in room temperature mobility from 395 to 520 cm2/Vs. The range in 3D mobility can be linked to increased dislocation densities in GaN grown on rougher BN templates. High 2DEG mobility ( 2000 cm2/Vs at 300 K) is achieved in AlGaN/GaN grown on atomically smooth BN templates, with a sheet electron density of 1×1013 cm-2, comparable to values obtained on conventional substrates. Samples grown on BN/sapphire showed mobilities (at 9 K) from 33000 cm2/Vs to 15200 cm2/Vs depending on BN roughness. The differences are associated with variations in AlGaN/GaN interface-roughness scattering and dislocation density due to the BN template morphology.

  12. Low-n-6 and low-n-6 plus high-n-3 diets for use in clinical research

    PubMed Central

    MacIntosh, Beth A.; Ramsden, Christopher E.; Faurot, Keturah R.; Zamora, Daisy; Mangan, Margaret; Hibbeln, Joseph R.; Mann, J. Douglas

    2014-01-01

    Few trials have evaluated the metabolic effects and health outcomes of lowering dietary n-6 PUFA. The objectives of the present paper were (1) to report the methods employed to lower dietary n-6 PUFA, while either increasing or maintaining n-3 PUFA intake and (2) to validate our methods with 24 h recalls and erythrocyte fatty acid analyses. A total of sixty-seven subjects were randomised to either (1) an average-n-3 PUFA, low-n-6 PUFA (L6) intervention designed to lower linoleic acid (LA; ≤2·5 % of energy (en%)) and arachidonic acid (≤60 mg/d), while maintaining an average US intake of n-3 PUFA or (2) a high-n-3 PUFA, low-n-6 PUFA (H3-L6) intervention designed to lower n-6 LA, while increasing the n-3 PUFA α-linolenic acid (ALA; ≥1·5 en%) and EPA + DHA (≥1000 mg/d). Pre- and intra-intervention nutrient intakes were estimated with six 24 h dietary recalls per subject. Both groups achieved the targeted reductions in dietary LA to ≤2·5 en% (median LA 2·45 (2·1, 3·1); P<0·001). Intakes of n-3 PUFA did not change for the L6 group. Target increases in n-3 ALA (median 1·6 en%, (1·3, 2·0), P<0·001) and EPA + DHA (1482 mg, (374, 2558), P<0·001) were achieved in the H3-L6 group. Dietary changes were validated by corresponding changes in erythrocyte n-6 and n-3 fatty acid composition. Dietary LA can be lowered to ≤2·5 en%, with or without concurrent increases in dietary n-3 PUFA, in an outpatient clinical trial setting using this integrated diet method. PMID:23328113

  13. Hydration and vibrational dynamics of betaine (N,N,N-trimethylglycine)

    NASA Astrophysics Data System (ADS)

    Li, Tanping; Cui, Yaowen; Mathaga, John; Kumar, Revati; Kuroda, Daniel G.

    2015-06-01

    Zwitterions are naturally occurring molecules that have a positive and a negative charge group in its structure and are of great importance in many areas of science. Here, the vibrational and hydration dynamics of the zwitterionic system betaine (N,N,N-trimethylglycine) is reported. The linear infrared spectrum of aqueous betaine exhibits an asymmetric band in the 1550-1700 cm-1 region of the spectrum. This band is attributed to the carboxylate asymmetric stretch of betaine. The potential of mean force computed from ab initio molecular dynamic simulations confirms that the two observed transitions of the linear spectrum are related to two different betaine conformers present in solution. A model of the experimental data using non-linear response theory agrees very well with a vibrational model comprising of two vibrational transitions. In addition, our modeling shows that spectral parameters such as the slope of the zeroth contour plot and central line slope are both sensitive to the presence of overlapping transitions. The vibrational dynamics of the system reveals an ultrafast decay of the vibrational population relaxation as well as the correlation of frequency-frequency correlation function (FFCF). A decay of ˜0.5 ps is observed for the FFCF correlation time and is attributed to the frequency fluctuations caused by the motions of water molecules in the solvation shell. The comparison of the experimental observations with simulations of the FFCF from ab initio molecular dynamics and a density functional theory frequency map shows a very good agreement corroborating the correct characterization and assignment of the derived parameters.

  14. Hydration and vibrational dynamics of betaine (N,N,N-trimethylglycine)

    PubMed Central

    Li, Tanping; Cui, Yaowen; Mathaga, John; Kumar, Revati; Kuroda, Daniel G.

    2015-01-01

    Zwitterions are naturally occurring molecules that have a positive and a negative charge group in its structure and are of great importance in many areas of science. Here, the vibrational and hydration dynamics of the zwitterionic system betaine (N,N,N-trimethylglycine) is reported. The linear infrared spectrum of aqueous betaine exhibits an asymmetric band in the 1550-1700 cm−1 region of the spectrum. This band is attributed to the carboxylate asymmetric stretch of betaine. The potential of mean force computed from ab initio molecular dynamic simulations confirms that the two observed transitions of the linear spectrum are related to two different betaine conformers present in solution. A model of the experimental data using non-linear response theory agrees very well with a vibrational model comprising of two vibrational transitions. In addition, our modeling shows that spectral parameters such as the slope of the zeroth contour plot and central line slope are both sensitive to the presence of overlapping transitions. The vibrational dynamics of the system reveals an ultrafast decay of the vibrational population relaxation as well as the correlation of frequency-frequency correlation function (FFCF). A decay of ∼0.5 ps is observed for the FFCF correlation time and is attributed to the frequency fluctuations caused by the motions of water molecules in the solvation shell. The comparison of the experimental observations with simulations of the FFCF from ab initio molecular dynamics and a density functional theory frequency map shows a very good agreement corroborating the correct characterization and assignment of the derived parameters. PMID:26049458

  15. Hydration and vibrational dynamics of betaine (N,N,N-trimethylglycine).

    PubMed

    Li, Tanping; Cui, Yaowen; Mathaga, John; Kumar, Revati; Kuroda, Daniel G

    2015-06-07

    Zwitterions are naturally occurring molecules that have a positive and a negative charge group in its structure and are of great importance in many areas of science. Here, the vibrational and hydration dynamics of the zwitterionic system betaine (N,N,N-trimethylglycine) is reported. The linear infrared spectrum of aqueous betaine exhibits an asymmetric band in the 1550-1700 cm(-1) region of the spectrum. This band is attributed to the carboxylate asymmetric stretch of betaine. The potential of mean force computed from ab initio molecular dynamic simulations confirms that the two observed transitions of the linear spectrum are related to two different betaine conformers present in solution. A model of the experimental data using non-linear response theory agrees very well with a vibrational model comprising of two vibrational transitions. In addition, our modeling shows that spectral parameters such as the slope of the zeroth contour plot and central line slope are both sensitive to the presence of overlapping transitions. The vibrational dynamics of the system reveals an ultrafast decay of the vibrational population relaxation as well as the correlation of frequency-frequency correlation function (FFCF). A decay of ∼0.5 ps is observed for the FFCF correlation time and is attributed to the frequency fluctuations caused by the motions of water molecules in the solvation shell. The comparison of the experimental observations with simulations of the FFCF from ab initio molecular dynamics and a density functional theory frequency map shows a very good agreement corroborating the correct characterization and assignment of the derived parameters.

  16. Consolidated Fleet N2Y-1

    NASA Technical Reports Server (NTRS)

    1930-01-01

    Consolidated Fleet N2Y-1: The Consolidated Fleet N2Y-1 aircraft were used as trainers for the pilots who would fly the 'parasite' fighters attached to the airships Akron and Macon. This N2Y-1 was turned over to the NACA for research work. Note that the vertical surfaces are instrumented for NACA work. This N2Y was used for landing gear tests.

  17. Intramolecular N-Glycan/Polypeptide Interactions Observed at Multiple N-Glycan Remodeling Steps through [13C,15N]-N-Acetylglucosamine Labeling of Immunoglobulin G1

    PubMed Central

    2014-01-01

    Asparagine-linked (N) glycosylation is a common eukaryotic protein modification that affects protein folding, function, and stability through intramolecular interactions between N-glycan and polypeptide residues. Attempts to characterize the structure–activity relationship of each N-glycan are hindered by inherent properties of the glycoprotein, including glycan conformational and compositional heterogeneity. These limitations can be addressed by using a combination of nuclear magnetic resonance techniques following enzymatic glycan remodeling to simultaneously generate homogeneous glycoforms. However, widely applicable methods do not yet exist. To address this technological gap, immature glycoforms of the immunoglobulin G1 fragment crystallizable (Fc) were isolated in a homogeneous state and enzymatically remodeled with [13C,15N]-N-acetylglucosamine (GlcNAc). UDP-[13C,15N]GlcNAc was synthesized enzymatically in a one-pot reaction from [13C]glucose and [15N-amido]glutamine. Modifying Fc with recombinantly expressed glycosyltransferases (Gnt1 and Gnt2) and UDP-[13C,15N]GlcNAc resulted in complete glycoform conversion as judged by mass spectrometry. Two-dimensional heteronuclear single-quantum coherence spectra of the Gnt1 product, containing a single [13C,15N]GlcNAc residue on each N-glycan, showed that the N-glycan is stabilized through interactions with polypeptide residues. Similar spectra of homogeneous glycoforms, halted at different points along the N-glycan remodeling pathway, revealed the presence of an increased level of interaction between the N-glycan and polypeptide at each step, including mannose trimming, as the N-glycan was converted to a complex-type, biantennary form. Thus, conformational restriction increases as Fc N-glycan maturation proceeds. Gnt1 and Gnt2 catalyze fundamental reactions in the synthesis of every glycoprotein with a complex-type N-glycan; thus, the strategies presented herein can be applied to a broad range of glycoprotein

  18. Electrochemical impedance spectroscopy of metal alloys in the space transportation system launch environment

    NASA Technical Reports Server (NTRS)

    Calle, Luz

    1990-01-01

    AC impedance measurements were performed to investigate the corrosion resistance of 18 alloys under conditions similar to the Space Transportation System (STS) launch environment. The alloys were: (1) zirconium 702; (2) Hastelloy C-22, C-276, C-4, and B-2; (3) Inconel 600 and 825; (4) Ferralium 255; (5) Inco Alloy G-3; (6) 20Cb-3; (7) SS 904L, 304LN, 316L, 317L, and 304L; (8) ES 2205; and (9) Monel 400. AC impedance data were gathered for each alloy at various immersion times in 3.55 percent NaCl-0.1N HCl. Polarization resistance values were obtained for the Nyguist plots at each immersion time using the EQUIVALENT CIRCUIT software package available with the 388 electrochemical impedance software. Hastelloy C-22 showed the highest overall values for polarization resistance while Monel 400 and Inconel 600 had the lowest overall values. There was good general correlation between the corrosion performance of the alloys at the beach corrosion testing site, and the expected rate of corrosion as predicted based on the polarization resistance values obtained. The data indicate that electrochemical impedance spectroscopy can be used to predict the corrosion performance of metal alloys.

  19. Utilisation of GaN and InGaN/GaN with nanoporous structures for water splitting

    SciTech Connect

    Benton, J.; Bai, J.; Wang, T.

    2014-12-01

    We report a cost-effective approach to the fabrication of GaN based nanoporous structure for applications in renewable hydrogen production. Photoelectrochemical etching in a KOH solution has been employed to fabricate both GaN and InGaN/GaN nanoporous structures with pore sizes ranging from 25 to 60 nm, obtained by controlling both etchant concentration and applied voltage. Compared to as-grown planar devices the nanoporous structures have exhibited a significant increase of photocurrent with a factor of up to four times. An incident photon conversion efficiency of up to 46% around the band edge of GaN has been achieved.

  20. Hydrogen Generation using non-polar coaxial InGaN/GaN Multiple Quantum Well Structure Formed on Hollow n-GaN Nanowires

    PubMed Central

    Park, Ji-Hyeon; Mandal, Arjun; Kang, San; Chatterjee, Uddipta; Kim, Jin Soo; Park, Byung-Guon; Kim, Moon-Deock; Jeong, Kwang-Un; Lee, Cheul-Ro

    2016-01-01

    This article demonstrates for the first time to the best of our knowledge, the merits of InGaN/GaN multiple quantum wells (MQWs) grown on hollow n-GaN nanowires (NWs) as a plausible alternative for stable photoelectrochemical water splitting and efficient hydrogen generation. These hollow nanowires are achieved by a growth method rather not by conventional etching process. Therefore this approach becomes simplistic yet most effective. We believe relatively low Ga flux during the selective area growth (SAG) aids the hollow nanowire to grow. To compare the optoelectronic properties, simultaneously solid nanowires are also studied. In this present communication, we exhibit that lower thermal conductivity of hollow n-GaN NWs affects the material quality of InGaN/GaN MQWs by limiting In diffusion. As a result of this improvement in material quality and structural properties, photocurrent and photosensitivity are enhanced compared to the structures grown on solid n-GaN NWs. An incident photon-to-current efficiency (IPCE) of around ~33.3% is recorded at 365 nm wavelength for hollow NWs. We believe that multiple reflections of incident light inside the hollow n-GaN NWs assists in producing a larger amount of electron hole pairs in the active region. As a result the rate of hydrogen generation is also increased. PMID:27556534

  1. The N-End Rule Pathway

    PubMed Central

    Tasaki, Takafumi; Sriram, Shashikanth M.; Park, Kyong Soo; Kwon, Yong Tae

    2013-01-01

    The N-end rule pathway is a proteolytic system in which N-terminal residues of short-lived proteins are recognized by recognition components (N-recognins) as essential components of degrons, called N-degrons. Known N-recognins in eukaryotes mediate protein ubiquitylation and selective proteolysis by the 26S proteasome. Substrates of N-recognins can be generated when normally embedded destabilizing residues are exposed at the N terminus by proteolytic cleavage. N-degrons can also be generated through modifications of posttranslationally exposed pro-N-degrons of otherwise stable proteins; such modifications include oxidation, arginylation, leucylation, phenylalanylation, and acetylation. Although there are variations in components, degrons, and hierarchical structures, the proteolytic systems based on generation and recognition of N-degrons have been observed in all eukaryotes and prokaryotes examined thus far. The N-end rule pathway regulates homeostasis of various physiological processes, in part, through interaction with small molecules. Here, we review the biochemical mechanisms, structures, physiological functions, and small-molecule-mediated regulation of the N-end rule pathway. PMID:22524314

  2. Hydrogen Generation using non-polar coaxial InGaN/GaN Multiple Quantum Well Structure Formed on Hollow n-GaN Nanowires

    NASA Astrophysics Data System (ADS)

    Park, Ji-Hyeon; Mandal, Arjun; Kang, San; Chatterjee, Uddipta; Kim, Jin Soo; Park, Byung-Guon; Kim, Moon-Deock; Jeong, Kwang-Un; Lee, Cheul-Ro

    2016-08-01

    This article demonstrates for the first time to the best of our knowledge, the merits of InGaN/GaN multiple quantum wells (MQWs) grown on hollow n-GaN nanowires (NWs) as a plausible alternative for stable photoelectrochemical water splitting and efficient hydrogen generation. These hollow nanowires are achieved by a growth method rather not by conventional etching process. Therefore this approach becomes simplistic yet most effective. We believe relatively low Ga flux during the selective area growth (SAG) aids the hollow nanowire to grow. To compare the optoelectronic properties, simultaneously solid nanowires are also studied. In this present communication, we exhibit that lower thermal conductivity of hollow n-GaN NWs affects the material quality of InGaN/GaN MQWs by limiting In diffusion. As a result of this improvement in material quality and structural properties, photocurrent and photosensitivity are enhanced compared to the structures grown on solid n-GaN NWs. An incident photon-to-current efficiency (IPCE) of around ~33.3% is recorded at 365 nm wavelength for hollow NWs. We believe that multiple reflections of incident light inside the hollow n-GaN NWs assists in producing a larger amount of electron hole pairs in the active region. As a result the rate of hydrogen generation is also increased.

  3. Mechanism of stress control for GaN growth on Si using AlN interlayers

    NASA Astrophysics Data System (ADS)

    Suzuki, Michihiro; Nakamura, Akihiro; Nakano, Yoshiaki; Sugiyama, Masakazu

    2017-04-01

    For the purpose of controlling the wafer bow of GaN-on-Si structure, in situ curvature transient during the growth of a GaN layer on an AlN interlayer was investigated systematically by estimating the compressive strain applied to the GaN layer with the progress of the layer growth. The compressive strain was dependent on the morphology of the GaN surface prior to the growth of the AlN interlayer. It was found that the transition sequence from GaN growth to AlN growth induces roughening of the GaN surface and both high NH3 partial pressure and the short transition time were effective for reducing the roughness of the GaN surface beneath the AlN interlayer. The improved transition sequence increased the compressive strain in GaN by a factor of 2.5. The AlN grown at the same temperature as that of GaN was beneficial in both better surface morphology and the reduction of the transition time between GaN growth and AlN growth. With this high-temperature AlN interlayer, its thickness is another important factor governing the compressive strain in GaN. To get AlN relaxed for applying the compressive strain to GaN, the AlN layer should be thicker but too thick layer after relaxation results in surface roughening, which in turn introduces defects to the overlying GaN layer and reduces the compressive strain by partial lattice relaxation of GaN.

  4. Au-free ohmic Ti/Al/TiN contacts to UID n-GaN fabricated by sputter deposition

    NASA Astrophysics Data System (ADS)

    Garbe, V.; Weise, J.; Motylenko, M.; Münchgesang, W.; Schmid, A.; Rafaja, D.; Abendroth, B.; Meyer, D. C.

    2017-02-01

    The fabrication and characterization of an Au-free Ti/Al/TiN (20/100/100 nm) contact stack to unintentionally doped n-GaN with TiN serving as the diffusion barrier is presented. Sputter deposition and lift-off in combination with post deposition annealing at 850 °C are used for contact formation. After annealing, contact shows ohmic behavior to n-GaN and a specific contact resistivity of 1.60 × 10-3 Ω cm2. To understand the contact formation on the microscopic scale, the contact was characterized by current-voltage measurements, linear transmission line method, X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. The results show the formation of Ti-N bonds at the GaN/Ti interface in the as-deposited stack. Annealing leads to diffusion of Ti, Al, Ga, and N, and the remaining metallic Ti is fully consumed by the formation of the intermetallic tetragonal Al3Ti phase. Native oxide from the GaN surface is trapped during annealing and accumulated in the Al interlayer. The TiN capping layer, however, was chemically stable during annealing. It prevented oxidation of the Ti/Al contact bilayer successfully and thus proved to be a well suitable diffusion barrier with ideal compatibility to the Ti/Al contact metallization.

  5. Semiconducting ZnSnN2 thin films for Si/ZnSnN2 p-n junctions

    NASA Astrophysics Data System (ADS)

    Qin, Ruifeng; Cao, Hongtao; Liang, Lingyan; Xie, Yufang; Zhuge, Fei; Zhang, Hongliang; Gao, Junhua; Javaid, Kashif; Liu, Caichi; Sun, Weizhong

    2016-04-01

    ZnSnN2 is regarded as a promising photovoltaic absorber candidate due to earth-abundance, non-toxicity, and high absorption coefficient. However, it is still a great challenge to synthesize ZnSnN2 films with a low electron concentration, in order to promote the applications of ZnSnN2 as the core active layer in optoelectronic devices. In this work, polycrystalline and high resistance ZnSnN2 films were fabricated by magnetron sputtering technique, then semiconducting films were achieved after post-annealing, and finally Si/ZnSnN2 p-n junctions were constructed. The electron concentration and Hall mobility were enhanced from 2.77 × 1017 to 6.78 × 1017 cm-3 and from 0.37 to 2.07 cm2 V-1 s-1, corresponding to the annealing temperature from 200 to 350 °C. After annealing at 300 °C, the p-n junction exhibited the optimum rectifying characteristics, with a forward-to-reverse ratio over 103. The achievement of this ZnSnN2-based p-n junction makes an opening step forward to realize the practical application of the ZnSnN2 material. In addition, the nonideal behaviors of the p-n junctions under both positive and negative voltages are discussed, in hope of suggesting some ideas to further improve the rectifying characteristics.

  6. Current transport property of n-GaN /n-6H-SiC heterojunction: Influence of interface states

    NASA Astrophysics Data System (ADS)

    Huang, Y.; Chen, X. D.; Fung, S.; Beling, C. D.; Ling, C. C.; Dai, X. Q.; Xie, M. H.

    2005-03-01

    Heterostructures of n-GaN /n-6H-SiC grown by hydride vapor phase epitaxy (HVPE) and molecular-beam epitaxy (MBE) are characterized with the current-voltage (I-V), capacitance-voltage (C-V), and deep level transient spectroscopy (DLTS) techniques. Using different contact configurations, the I -V results reveal a rectifying barrier in the n-GaN /n-6H-SiC heterostructures. When GaN is negatively biased, the current is exponentially proportional to the applied voltage with the built-in barrier being 0.4-1.1eV for the HVPE samples and 0.5eV for the MBE sample. DLTS measurements reveal intense band-like deep level states in the interfacial region of the heterostructure, and the Fermi-level pinning by these deep level defects is invoked to account for the interfacial rectifying barrier of the heterostructures.

  7. Epitaxial stabilization of cubic-SiN{sub x} in TiN/SiN{sub x} multilayers

    SciTech Connect

    Soederberg, Hans; Oden, Magnus; Larsson, Tommy; Hultman, Lars; Molina-Aldareguia, Jon M.

    2006-05-08

    The formation of cubic-phase SiN{sub x} is demonstrated in TiN/SiN{sub x} multilayers deposited by reactive dual magnetron sputtering. Transmission electron microscopy examination shows a transition from epitaxially stabilized growth of crystalline SiN{sub x} to amorphous growth as the layer thickness increases from 0.3 to 0.8 nm. The observations are supported by ab initio calculations on different polytypes, which show that the NaCl structure has the best lattice match to TiN. Calculations also reveal a large difference in elastic shear modulus between NaCl-SiN{sub x} and TiN. The results for phase structure and shear modulus offer an explanation for the superhardening effect determined by nanoindentation experiments.

  8. Alloys For Flexible Hoses In A Corrosive Environment

    NASA Technical Reports Server (NTRS)

    Macdowell, Louis G., III; Ontiveros, Cordelia

    1992-01-01

    High-nickel alloy resists pitting corrosion. Report evaluates metal alloys for flexible hoses in corrosive environment. Tested to find alternatives to 304L stainless steel. Nineteen alloys selected for testing on basis of reputation for resistance to corrosion. Top five, in order of decreasing resistance to corrosion: Hastelloy(R) C-22, Inconel(R) 625, Hastelloy(R) C-276, Hastelloy(R) C-4, and Inco(R) alloy G-3. Of these, Hastelloy(R) C-22 found best for flexible-hose application.

  9. 78 FR 42584 - Bureau of International Security and Nonproliferation: Report to Congress Pursuant to Section...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-16

    ..., military, or ballistic missile programs of Iran: aluminum; beryllium; boron; cobalt; copper; copper infiltrated tungsten; copper- beryllium; graphite; hastelloy; inconel; magnesium; molybdenum; nickel;...

  10. Reactions of N-chloramines and N-haloamides with unsaturated compounds

    NASA Astrophysics Data System (ADS)

    Mirskova, Anna N.; Drozdova, Tat'yana I.; Levkovskaya, Galina G.; Voronkov, Mikhail G.

    1989-03-01

    The results obtained from studying the reactions of N-chloramines, N-halocarbamates, and N-haloamides of carboxylic, sulphonic, and phosphoric acids with unsaturated compounds have been correlated and classified. It is shown that the direction of addition of N-haloamines and N-haloamides to alkenes, dienes, alkenynes, and acetylenes, giving saturated adducts, is determined by the conditions of homolytic or heterolytic initiation. The reactions of N-chlorodialkylamines with olefins in the presence of sulphur trioxide are discussed. A new method of activating electrophilic reagents by introducing sulphur trioxide on to the N-Cl bond is identified. An essentially new trend is reported for the reactions of N,N-dihaloamides of sulphonic and carboxylic acids and also N,N-dihalocarbamates with polyhaloethylenes, giving acylimines of polyhaloaldehydes, which are highly reactive syntones for the synthesis of fine organic chemicals. The bibliography includes 216 references.

  11. Infrared spectra of the Ne2-N2O, Ar2-N2O trimers

    NASA Astrophysics Data System (ADS)

    Rezaei, M.; Michaelian, K. H.; McKellar, A. R. W.; Moazzen-Ahmadi, N.

    2012-08-01

    Spectra of the van der Waals trimers Ar2-N2O and Ne2-N2O are studied in the region of the N2O ν1 fundamental (≈2220 cm-1) using a tunable quantum cascade laser to probe a pulsed supersonic expansion from a slit jet nozzle. Improved data are obtained for the dimers Ar-N2O and Ne-N2O, and the Q-branch of Ar3-N2O is tentatively assigned. The vibrational shifts for Nen-N2O are almost exactly linear for n = 0-2. However, for Arn-N2O the n = 2 band origin is slightly blue-shifted compared to the linear prediction, and the n = 3 origin (if correct) is more significantly blue-shifted (by 0.09 cm-1).

  12. Technical Note: Simultaneous measurement of sedimentary N2 and N2O production and new 15N isotope pairing technique

    NASA Astrophysics Data System (ADS)

    Hsu, T.-C.; Kao, S.-J.

    2013-04-01

    Dinitrogen (N2) and/or nitrous oxide (N2O) are produced through denitrification, anaerobic ammonium oxidation (anammox) or nitrification in sediments, of which entangled processes obfuscate the absolute rate estimation of gaseous nitrogen production from individual pathway. Recently, the classical isotope pairing technique (IPT), the most common 15N-nitrate enrichment method to quantify denitrification, has been modified by different researchers to (1) discriminate relative contribution of N2 production by denitrification from anammox or to (2) provide more accurate denitrification rate by considering both N2O and N2 productions. Both modified methods, however, have deficiencies such as overlooking N2O production in case 1 and neglecting anammox in case 2. In this paper, a new method was developed to refine previous methods. We installed cryogenic traps to pre-concentrate N2 and N2O separately, thus, allowing simultaneous measurement for two gases generated by one sample. The precision is better than 2% for N2 (m/z 28, m/z 29 and m/z 30), and 1.5% for N2O (m/z 44, m/z 45 and m/z 46). Based on the six m/z peaks of the two gases, we further revised IPT formulae to truthfully resolve the production rates of N2 and N2O contributed from 3 specific nitrogen removal processes, i.e. N2 and N2O from denitrification, N2 from anammox and N2O from nitrification. To validate the applicability of our new method, incubation experiments were conducted using sediment cores taken from the Danshuei estuary in Taiwan. We successfully determined the rates of aforementioned nitrogen removal processes. Moreover, N2O yield was as high as 66%, which no doubt would significantly bias previous IPT approaches when N2O was not considered. Our new method not only complements the previous IPT but also provides more comprehensive information to advance our understanding of nitrogen dynamics through the water-sediment interface.

  13. N*ews from COSY

    NASA Astrophysics Data System (ADS)

    Ströher, Hans

    2012-04-01

    COSY, a storage and cooler synchrotron, which is fed by an injector cyclotron, is operated at Forschungszentrum Jülich (Germany). It provides phase space cooled polarized or unpolarized beams of protons and deuterons with momenta between 0.3 and 3.7 GeV/c for internal experiments and to external target stations. The major experimental facilities, used for the ongoing physics program, are ANKE and WASA (internal) and TOF (external). A new internal target station to investigate polarization build-up by spin-filtering (PAX) has recently been commissioned. COSY is the machine for hadron spin physics on a world-wide scale, which in recent times is also used for tests in conjunction with plans to build a dedicated storage ring for electric dipole moment (EDM) measurements of proton, deuteron and 3He. In this contribution selected experimental results from the N*-program are presented.

  14. Effect of feeding system and breed on n-3 and n-6 polyunsaturated fatty acid content of lamb muscles

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Katahdin (KK, n=6), Katahdin x Suffolk (KS, n=6), Suffolk x Katahdin (SK, n=6) and Suffolk (SS, n=6) wethers were used to evaluate omega-3 (n-3) and omega-6 (n-6) polyunsaturated fatty acid content, and the ratio of n-6 to n-3 in muscles of these lambs, raised on concentrate or forage diets. Lambs ...

  15. Sweetwater, Texas Large N Experiment

    NASA Astrophysics Data System (ADS)

    Sumy, D. F.; Woodward, R.; Barklage, M.; Hollis, D.; Spriggs, N.; Gridley, J. M.; Parker, T.

    2015-12-01

    From 7 March to 30 April 2014, NodalSeismic, Nanometrics, and IRIS PASSCAL conducted a collaborative, spatially-dense seismic survey with several thousand nodal short-period geophones complemented by a backbone array of broadband sensors near Sweetwater, Texas. This pilot project demonstrates the efficacy of industry and academic partnerships, and leveraged a larger, commercial 3D survey to collect passive source seismic recordings to image the subsurface. This innovative deployment of a large-N mixed-mode array allows industry to explore array geometries and investigate the value of broadband recordings, while affording academics a dense wavefield imaging capability and an operational model for high volume instrument deployment. The broadband array consists of 25 continuously-recording stations from IRIS PASSCAL and Nanometrics, with an array design that maximized recording of horizontal-traveling seismic energy for surface wave analysis over the primary target area with sufficient offset for imaging objectives at depth. In addition, 2639 FairfieldNodal Zland nodes from NodalSeismic were deployed in three sub-arrays: the outlier, backbone, and active source arrays. The backbone array consisted of 292 nodes that covered the entire survey area, while the outlier array consisted of 25 continuously-recording nodes distributed at a ~3 km distance away from the survey perimeter. Both the backbone and outlier array provide valuable constraints for the passive source portion of the analysis. This project serves as a learning platform to develop best practices in the support of large-N arrays with joint industry and academic expertise. Here we investigate lessons learned from a facility perspective, and present examples of data from the various sensors and array geometries. We will explore first-order results from local and teleseismic earthquakes, and show visualizations of the data across the array. Data are archived at the IRIS DMC under stations codes XB and 1B.

  16. TiTaN Reconsidered

    NASA Astrophysics Data System (ADS)

    Natland, J. H.

    2008-12-01

    Strongly positive TiO2, Ta, and Nb (TiTaN) anomalies (1) in a Samoan ankaramite from Ofu Island have been attributed to the presence of refractory yet titanian eclogite in the mantle source. From chemical compositions, however, the anomalies could instead result from concentration of phenocrysts in magmas produced by mixing between a highly differentiated alkalic basalt and a crystal sludge carrying abundant olivine, clinopyroxene and especially titanomagnetite phenocrysts, the latter producing much of the TiTaN anomalies, and behaving much like rutile in eclogite. This is consistent with petrography. The distinctive effects of addition of each mineral are well illustrated on major-oxide variation diagrams. Separation of these minerals from liquids (to concentrate in ankaramites and dunite-wehrlite-pyroxenite cumulates) beginning at about 0.15 GPa in the mantle produces residual felsic differentiates (hawaiites, mugearites) with low TiTan anomalies (<1), exemplified by samples dredged elsewhere in Samoa from Savai'i (2). The Ofu samples have a low EMII signature (high 3He/4He), whereas the Savai'i samples have a high EMII signature (low 3He/4He), the extremes at Samoa. This gives a coincidental positive correlation at Samoa overall between TiTan anomalies and 3He/4He, TiTan anomalies being accentuated at the two places by the contrasting effects of phenocryst addition and subtraction during differentiation. High 3He/4He beneath several eastern Samoan volcanoes appears to be an attribute of near-FOZO mantle sources with minimal EM2 signature. (1) Jackson, M., et al., 2008. G-Cubed 9: doi:1029/2007GC001876 (2) Jackson, M., et al., 2007, Nature 448: 684-687, doi:10.1038/nature060488

  17. HC3N observations of nearby galaxies

    NASA Astrophysics Data System (ADS)

    Jiang, Xue-Jian; Wang, Jun-Zhi; Gao, Yu; Gu, Qiu-Sheng

    2017-03-01

    Aims: We aim to systematically study the properties of the different transitions of the dense molecular gas tracer HC3N in galaxies. Methods: We have conducted single-dish observations of HC3N emission lines towards a sample of nearby gas-rich galaxies. HC3N(J = 2-1) was observed in 20 galaxies with the Effelsberg 100-m telescope. HC3N(J = 24-23) was observed in nine galaxies with the 10-m Submillimeter Telescope (SMT). Results: HC3N 2-1 is detected in three galaxies: IC 342, M 66, and NGC 660 (> 3σ). HC3N 24-23 is detected in three galaxies: IC 342, NGC 1068, and IC 694. These are the first measurements of HC3N 2-1 in a relatively large sample of external galaxies, although the detection rate is low. For the HC3N 2-1 non-detections, upper limits (2σ) are derived for each galaxy, and stacking the non-detections is attempted to recover the weak signal of HC3N. The stacked spectrum, however, does not show any significant signs of HC3N 2-1 emission. The results are also compared with other transitions of HC3N observed in galaxies. Conclusions: The low detection rate of both transitions suggests low abundance of HC3N in galaxies, which is consistent with other observational studies. The comparison between HC3N and HCN or HCO+shows a large diversity in the ratios between HC3N and HCN or HCO+. More observations are needed to interpret the behavior of HC3N in different types of galaxies.

  18. [Determination of Influenza Virus H5N1 and H7N9 Using MASA Technology].

    PubMed

    Yuan, Jing; Bao, Linlin; Wei, Qiang; Qin, Chuan; Xu, Lili

    2015-11-01

    To set up a new rapid method for the rapid determination of influenza virus H5N1 and H7N9 basing on the Multi-Analyte Suspension Array (MASA) technology. Sequence analysis and design of degenerate primers and specific probes were set in the comparison and analysis of H5, N1, H7 and N9 genes. In combination with MASA technology, these primers and probes were used for the determination of samples of H5N1 and H7N9 and other subtypes ( H1N1, PH1N1, H5N2, H3N2 and H9N2). We developed a rapid determination method. This method had high specificity and sensitivity that could detect H5N1 and H7N9 at one time, and could detect samples that containing 10 copies of H5N1 and H7N9. This determination method could be used for rapid determination of influenza virus H5N1 and H7N9 at one time.

  19. Dynamical coupled-channels study of pi N --> pi pi N reactions

    SciTech Connect

    Kamano, Hiroyuki; Julia Diaz, Bruno; Lee, Tsung-Shung; Matsuyama, Akihiko; Sato, Toru

    2009-01-01

    As a step toward performing a complete coupled-channels analysis of the world data of pi N, gamma^* N --> pi N, eta N, pi pi N reactions, the pi N --> pi pi N reactions are investigated starting with the dynamical coupled-channels model developed in Phys. Rev. C76, 065201 (2007). The channels included are pi N, eta N, and pi pi N which has pi Delta, rho N, and sigma N resonant components. The non-resonant amplitudes are generated from solving a set of coupled-channels equations with the meson-baryon potentials defined by effective Lagrangians. The resonant amplitudes are generated from 16 bare excited nucleon (N^*) states which are dressed by the non-resonant interactions as constrained by the unitarity condition. The available total cross section data of pi^+ p --> pi^+ pi^+ n, pi^+ pi^0 and pi^- p --> pi^+ pi^- n, pi^- pi^0 n, pi^0 pi^0 n can be reproduced to a very large extent both in magnitudes and energy-dependence. Possible improvements of the model are investigated, in p

  20. Amplitude for N-gluon superstring scattering.

    PubMed

    Stieberger, Stephan; Taylor, Tomasz R

    2006-11-24

    We consider scattering processes involving N gluonic massless states of open superstrings with a certain Regge slope alpha'. At the semiclassical level, the string world-sheet sweeps a disk and N gluons are created or annihilated at the boundary. We present exact expressions for the corresponding amplitudes, valid to all orders in alpha', for the so-called maximally helicity violating configurations, with N = 4, 5 and N = 6. We also obtain the leading O(alpha '2) string corrections to the zero-slope N-gluon Yang-Mills amplitudes.

  1. Amplitude for N-Gluon Superstring Scattering

    SciTech Connect

    Stieberger, Stephan; Taylor, Tomasz R.

    2006-11-24

    We consider scattering processes involving N gluonic massless states of open superstrings with a certain Regge slope {alpha}{sup '}. At the semiclassical level, the string world-sheet sweeps a disk and N gluons are created or annihilated at the boundary. We present exact expressions for the corresponding amplitudes, valid to all orders in {alpha}{sup '}, for the so-called maximally helicity violating configurations, with N=4, 5 and N=6. We also obtain the leading O({alpha}{sup '2}) string corrections to the zero-slope N-gluon Yang-Mills amplitudes.

  2. On special classes of n-algebras

    NASA Astrophysics Data System (ADS)

    Vainerman, L.; Kerner, R.

    1996-05-01

    We define n-algebras as linear spaces on which the internal composition law involves n elements: m:V⊗n■V. It is known that such algebraic structures are interesting for their applications to problems of modern mathematical physics. Using the notion of a commutant of two subalgebras of an n-algebra, we distinguish certain classes of n-algebras with reasonable properties: semisimple, Abelian, nilpotent, solvable. We also consider a few examples of n-algebras of different types, and show their properties.

  3. Metal-interconnection-free integration of InGaN/GaN light emitting diodes with AlGaN/GaN high electron mobility transistors

    SciTech Connect

    Liu, Chao; Cai, Yuefei; Liu, Zhaojun; Ma, Jun; Lau, Kei May

    2015-05-04

    We report a metal-interconnection-free integration scheme for InGaN/GaN light emitting diodes (LEDs) and AlGaN/GaN high electron mobility transistors (HEMTs) by combining selective epi removal (SER) and selective epitaxial growth (SEG) techniques. SER of HEMT epi was carried out first to expose the bottom unintentionally doped GaN buffer and the sidewall GaN channel. A LED structure was regrown in the SER region with the bottom n-type GaN layer (n-electrode of the LED) connected to the HEMTs laterally, enabling monolithic integration of the HEMTs and LEDs (HEMT-LED) without metal-interconnection. In addition to saving substrate real estate, minimal interface resistance between the regrown n-type GaN and the HEMT channel is a significant improvement over metal-interconnection. Furthermore, excellent off-state leakage characteristics of the driving transistor can also be guaranteed in such an integration scheme.

  4. Metal-interconnection-free integration of InGaN/GaN light emitting diodes with AlGaN/GaN high electron mobility transistors

    NASA Astrophysics Data System (ADS)

    Liu, Chao; Cai, Yuefei; Liu, Zhaojun; Ma, Jun; Lau, Kei May

    2015-05-01

    We report a metal-interconnection-free integration scheme for InGaN/GaN light emitting diodes (LEDs) and AlGaN/GaN high electron mobility transistors (HEMTs) by combining selective epi removal (SER) and selective epitaxial growth (SEG) techniques. SER of HEMT epi was carried out first to expose the bottom unintentionally doped GaN buffer and the sidewall GaN channel. A LED structure was regrown in the SER region with the bottom n-type GaN layer (n-electrode of the LED) connected to the HEMTs laterally, enabling monolithic integration of the HEMTs and LEDs (HEMT-LED) without metal-interconnection. In addition to saving substrate real estate, minimal interface resistance between the regrown n-type GaN and the HEMT channel is a significant improvement over metal-interconnection. Furthermore, excellent off-state leakage characteristics of the driving transistor can also be guaranteed in such an integration scheme.

  5. Optical properties of GaN pyramids

    SciTech Connect

    Zeng, K.C.; Lin, J.Y.; Jiang, H.X.; Yang, W.

    1999-03-01

    Picosecond time-resolved photoluminescence (PL) spectroscopy has been used to investigate the optical properties of GaN pyramids overgrown on hexagonal-patterned GaN(0001) epilayers on sapphire and silicon substrates with AlN buffer layers. We found that: (i) the release of the biaxial compressive strain in GaN pyramids on GaN/AlN/sapphire substrate led to a 7 meV redshift of the spectral peak position with respect to the strained GaN epilayer grown under identical conditions; (ii) in the GaN pyramids on GaN/AlN/sapphire substrate, strong band edge transitions with much narrower linewidths than those in the GaN epilayer have been observed, indicating the improved crystalline quality of the overgrown pyramids; (iii) PL spectra taken from different parts of the pyramids revealed that the top of the pyramid had the highest crystalline quality; and (iv) the presence of strong band-to-impurity transitions in the pyramids were primarily due to the incorporation of the oxygen and silicon impurities from the SiO{sub 2} mask. {copyright} {ital 1999 American Institute of Physics.}

  6. [Influenza pandemic (H1N1) 2009].

    PubMed

    Oshitani, Hitoshi

    2009-12-01

    In the past, influenza pandemics have been occurring every 20 to 30 years. Highly pathogenic avian influenza A(H5N1) has been causing unprecedented global outbreaks since 2003 and many human cases with a high case fatality rate have also been reported. But the virus that caused a pandemic in 2009 was A(H1N1) that was originated from swine influenza. The same subtype, A(H1N1) has been circulating in human population since 1977. This pandemic (H1N1) 2009 is also not as virulent as A(H5N1) in humans. Many aspects of pandemic (H1N1) 2009 are different from what we had been expecting. We should reconsider the concepts and the strategies for influenza pandemic by reviewing current pandemic (H1N1).

  7. Modern comparative approach for carrier transport in InAlN/AlN superlattice device with characteristics and modelling using nitride (14N,15N) isotopes

    NASA Astrophysics Data System (ADS)

    Mazumdar, Kaushik; Ranjan, Rajeev Kumar; Shankar, Ravi; Priyadarshini, Bindu; Ghosal, Aniruddha

    2017-03-01

    As we all know that, the performance and characteristics of any semiconductor device are effected by change in operating temperature. The temperature dependencies of the transport properties of InAlN/Al14N15N have been investigated using theoretical and mathematical study. Here we have considered the Al14N15N with different ratio of 14N and 15N for the analysis owing to considerable interest in superlattice structures of large band gap semiconductors having various favourable material properties such as very high thermal conductivity, high carrier mobility and wide bandwidth operation. This paper deals with analysis of temperature effect on some of the device modelling parameters like carrier mobility and scattering.

  8. Improved electrical properties of n-n and p-n Si/SiC junctions with thermal annealing treatment

    NASA Astrophysics Data System (ADS)

    Liang, J.; Nishida, S.; Arai, M.; Shigekawa, N.

    2016-07-01

    The effects of annealing process on the electrical properties of n+-Si/n-SiC and p+-Si/n-SiC junctions fabricated by using surface-activated bonding are investigated. It is found by measuring the current-voltage (I-V) characteristics of n+-Si/n-SiC junctions that the reverse-bias current and the ideality factor decreased to 2.0 × 10-5 mA/cm2 and 1.10, respectively, after the junctions annealing at 700 °C. The flat band voltages of n+-Si/n-SiC and p+-Si/n-SiC junctions obtained from capacitance-voltage (C-V) measurements decreased with increasing annealing temperature. Furthermore, their flat band voltages are very close to each other irrespective of the annealing temperature change, which suggests that the Fermi level is still pinned at the bonding interface even for the junctions annealing at high temperature and the interface state density causing Fermi level pinning varies with the junctions annealing. The reverse characteristics of n+-Si/n-SiC junctions are in good agreement with the calculations based on thermionic field emission. In addition, the calculated donor concentration of 4H-SiC epi-layers and flat band voltage is consistent with the values obtained from C-V measurements.

  9. AlGaN/GaN high electron mobility transistors with selective area grown p-GaN gates

    NASA Astrophysics Data System (ADS)

    Yuliang, Huang; Lian, Zhang; Zhe, Cheng; Yun, Zhang; Yujie, Ai; Yongbing, Zhao; Hongxi, Lu; Junxi, Wang; Jinmin, Li

    2016-11-01

    We report a selective area growth (SAG) method to define the p-GaN gate of AlGaN/GaN high electron mobility transistors (HEMTs) by metal-organic chemical vapor deposition. Compared with Schottky gate HEMTs, the SAG p-GaN gate HEMTs show more positive threshold voltage (V th) and better gate control ability. The influence of Cp2Mg flux of SAG p-GaN gate on the AlGaN/GaN HEMTs has also been studied. With the increasing Cp2Mg from 0.16 μmol/min to 0.20 μmol/min, the V th raises from -0.67 V to -0.37 V. The maximum transconductance of the SAG HEMT at a drain voltage of 10 V is 113.9 mS/mm while that value of the Schottky HEMT is 51.6 mS/mm. The SAG method paves a promising way for achieving p-GaN gate normally-off AlGaN/GaN HEMTs without dry etching damage. Project supported by the National Natural Sciences Foundation of China (Nos. 61376090, 61306008) and the National High Technology Program of China (No. 2014AA032606).

  10. Antidepressant Potential of 5-HT3 Receptor Antagonist, N-n- propyl-3-ethoxyquinoxaline-2-carboxamide (6n).

    PubMed

    Mahesh, R; Bhatt, S; Devadoss, T; Jindal, Ak; Gautam, Bk; Pandey, Dk

    2012-10-01

    The present study was designed to evaluate the antidepressant potential of 5-HT3 receptor antagonist N-n-propyl-3-ethoxyquinoxaline-2-carboxamide (6n). The compound '6n' with optimum log P and pA 2 value identified from a series of compounds synthesized in our laboratory was subjected to forced Swim Test (FST) (1, 2, and 4 mg/kg, i.p) and Tail Suspension Test (TST) (1, 2, and 4 mg/kg, i.p.). The compound '6n' significantly reduced the duration of immobility in mice without affecting the baseline locomotion. Moreover, '6n' (2 mg/kg, i.p.) potentiated the 5-hydroxytryptophan (5-HTP)-induced head twitch responses in mice and '6n' at tested dose (1 and 2 mg/kg, i.p.) reversed the reserpine-induced hypothermia in rats. In interaction studies of '6n' with various standard drugs/ligands using FST, '6n' (1 mg/kg, i.p.) potentiated the antidepressant effect of venlafaxine (4 and 8 mg/kg, i.p.) and fluoxetine (10 and 20 mg/kg, i.p.). Additionally, '6n' (1 and 2 mg/kg, i.p.) influenced the effect of harmane (5 mg/ kg, i.p.) as well as reversed the effect of parthenolide (1 mg/kg, i.p.) by reducing the duration of immobility in FST. Furthermore, '6n' (1 mg/kg, i.p.) potentiated the effect of bupropion (10 and 20 mg/kg, i.p.) in TST. Chronic '6n' (1 and 2 mg/kg, i.p.) treatment attenuated the behavioral abnormalities in olfactory bulbectomized rats. In conclusion, these various findings reiterated the antidepressant-like effects of '6n' in behavioral models of depression.

  11. Glacial-Interglacial and Holocene N2O Stable Isotope Changes Constrain Terrestrial N Cycling

    NASA Astrophysics Data System (ADS)

    Schmitt, J.; Spahni, R.; Bock, M.; Seth, B.; Stocker, B. D.; Ri, X.; Schilt, A.; Brook, E.; Otto-Bliesner, B. L.; Liu, Z.; Prentice, I. C.; Fischer, H.; Joos, F.

    2015-12-01

    The land biosphere contributes most to the natural source of the long-lived greenhouse gas nitrous oxide (N2O), with N2O emissions being dependent on the turnover rate of both the terrestrial nitrogen (N) and carbon (C) cycle. The C:N stoichiometry of vegetation and soil organic matter links the cycles intimately. Sustained plant productivity increase must be supported by biological N fixation. Intensified N cycling in turn enhances N loss and thereby N2O emissions. The temporal and spatial dynamics of terrestrial N and C cycles and related terrestrial N2O emissions are poorly constrained over the glacial-interglacial transition and the Holocene. Here we reconstruct increased terrestrial N2O emissions since the Last Glacial Maximum based on N2O concentration and isotope measurements on several ice cores and show that this N2O increase can be explained by N cycle modelling - provided N fixation is allowed to respond dynamically to increasing N demand and turnover. The Ice core reconstructions suggest a deglacial increase of 1.1 ± 0.4 Tg N/yr in terrestrial and 0.6 ± 0.4 Tg/yr in oceanic N2O emissions, but relatively constant terrestrial emissions over the Holocene. Transient simulations with a Dynamic Global Vegetation Model are shown to represent the climate and CO2 induced changes in terrestrial N2O emission, and suggest a deglacial increase in biological N fixation by 20%, independently of its absolute magnitude. Deciphering the response of biological N fixation during climatic changes is an important factor for our understanding of plant growth and the land carbon sink, alongside anthropogenic greenhouse gas emissions.

  12. Ecosystem N distribution and δ15N during a century of forest regrowth after agricultural abandonment

    USGS Publications Warehouse

    Compton, J.E.; Hooker, T.D.; Perakis, S.S.

    2007-01-01

    Stable isotope ratios of terrestrial ecosystem nitrogen (N) pools reflect internal processes and input–output balances. Disturbance generally increases N cycling and loss, yet few studies have examined ecosystem δ15N over a disturbance-recovery sequence. We used a chronosequence approach to examine N distribution and δ15N during forest regrowth after agricultural abandonment. Site ages ranged from 10 to 115 years, with similar soils, climate, land-use history, and overstory vegetation (white pine Pinus strobus). Foliar N and δ15N decreased as stands aged, consistent with a progressive tightening of the N cycle during forest regrowth on agricultural lands. Over time, foliar δ15N became more negative, indicating increased fractionation along the mineralization–mycorrhizal–plant uptake pathway. Total ecosystem N was constant across the chronosequence, but substantial internal N redistribution occurred from the mineral soil to plants and litter over 115 years (>25% of ecosystem N or 1,610 kg ha−1). Temporal trends in soil δ15N generally reflected a redistribution of depleted N from the mineral soil to the developing O horizon. Although plants and soil δ15N are coupled over millennial time scales of ecosystem development, our observed divergence between plants and soil suggests that they can be uncoupled during the disturbance-regrowth sequence. The approximate 2‰ decrease in ecosystem δ15N over the century scale suggests significant incorporation of atmospheric N, which was not detected by traditional ecosystem N accounting. Consideration of temporal trends and disturbance legacies can improve our understanding of the influence of broader factors such as climate or N deposition on ecosystem N balances and δ15N.

  13. 40 CFR 721.3848 - Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-, monosodium salt. 721.3848 Section 721.3848 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3848 Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt. (a... glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt (PMN P-00-469; CAS No. 141321-68-8) is subject...

  14. 40 CFR 721.520 - Alanine, N-(2-carboxyethyl)-N-alkyl-, salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-, salt. 721.520 Section 721.520 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.520 Alanine, N-(2-carboxyethyl)-N-alkyl-, salt. (a) Chemical substance... alanine, N-(2-carboxyethyl)-N- alkyl-, salt (P-89-336) is subject to reporting under this section for...

  15. 40 CFR 721.3848 - Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-, monosodium salt. 721.3848 Section 721.3848 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3848 Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt. (a... glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt (PMN P-00-469; CAS No. 141321-68-8) is subject...

  16. 40 CFR 721.520 - Alanine, N-(2-carboxyethyl)-N-alkyl-, salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-, salt. 721.520 Section 721.520 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.520 Alanine, N-(2-carboxyethyl)-N-alkyl-, salt. (a) Chemical substance... alanine, N-(2-carboxyethyl)-N- alkyl-, salt (P-89-336) is subject to reporting under this section for...

  17. 40 CFR 721.1085 - Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Benzenamine,4,4â²-methylenebis[N-ethyl-N-methyl-. 721.1085 Section 721.1085 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.1085 Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-. (a)...

  18. 40 CFR 721.4080 - MNNG (N-methyl-N′-nitro-N-nitrosoguanidine).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false MNNG (N-methyl-Nâ²-nitro-N... Specific Chemical Substances § 721.4080 MNNG (N-methyl-N′-nitro-N-nitrosoguanidine). (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance MNNG...

  19. 40 CFR 721.225 - 2-Chloro-N-methyl-N-substituted acetamide (generic name).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false 2-Chloro-N-methyl-N-substituted... Specific Chemical Substances § 721.225 2-Chloro-N-methyl-N-substituted acetamide (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance...

  20. 40 CFR 721.1085 - Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Benzenamine,4,4â²-methylenebis[N-ethyl-N-methyl-. 721.1085 Section 721.1085 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.1085 Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-. (a)...

  1. 40 CFR 721.1085 - Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Benzenamine,4,4â²-methylenebis[N-ethyl-N-methyl-. 721.1085 Section 721.1085 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.1085 Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-. (a)...

  2. 40 CFR 721.4080 - MNNG (N-methyl-N′-nitro-N-nitrosoguanidine).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false MNNG (N-methyl-Nâ²-nitro-N... Specific Chemical Substances § 721.4080 MNNG (N-methyl-N′-nitro-N-nitrosoguanidine). (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance MNNG...

  3. 40 CFR 721.4080 - MNNG (N-methyl-N′-nitro-N-nitrosoguanidine).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false MNNG (N-methyl-Nâ²-nitro-N... Specific Chemical Substances § 721.4080 MNNG (N-methyl-N′-nitro-N-nitrosoguanidine). (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance MNNG...

  4. 40 CFR 721.4080 - MNNG (N-methyl-N′-nitro-N-nitrosoguanidine).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false MNNG (N-methyl-Nâ²-nitro-N... Specific Chemical Substances § 721.4080 MNNG (N-methyl-N′-nitro-N-nitrosoguanidine). (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance MNNG...

  5. 40 CFR 721.225 - 2-Chloro-N-methyl-N-substituted acetamide (generic name).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false 2-Chloro-N-methyl-N-substituted... Specific Chemical Substances § 721.225 2-Chloro-N-methyl-N-substituted acetamide (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance...

  6. 40 CFR 721.1085 - Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Benzenamine,4,4â²-methylenebis[N-ethyl-N-methyl-. 721.1085 Section 721.1085 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.1085 Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-. (a)...

  7. 40 CFR 721.225 - 2-Chloro-N-methyl-N-substituted acetamide (generic name).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false 2-Chloro-N-methyl-N-substituted... Specific Chemical Substances § 721.225 2-Chloro-N-methyl-N-substituted acetamide (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance...

  8. Copper-catalyzed aminooxygenation of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives

    PubMed Central

    Li, Yan; Zhou, Xue; Zheng, Guangfan

    2015-01-01

    Summary A copper-catalyzed aminooxygenation reaction of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives has been developed. The aminooxygenation product could be converted into the corresponding alcohol or free amine through the cleavage of the N–O or C–N bond of the N-hydroxyphthalimide moiety. PMID:26877794

  9. 40 CFR 721.3848 - Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-, monosodium salt. 721.3848 Section 721.3848 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3848 Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt. (a... glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt (PMN P-00-469; CAS No. 141321-68-8) is subject...

  10. 40 CFR 721.3848 - Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-, monosodium salt. 721.3848 Section 721.3848 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3848 Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt. (a... glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt (PMN P-00-469; CAS No. 141321-68-8) is subject...

  11. 40 CFR 721.3848 - Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-, monosodium salt. 721.3848 Section 721.3848 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3848 Glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt. (a... glycine, N-(carboxymethyl)-N-dodecyl-, monosodium salt (PMN P-00-469; CAS No. 141321-68-8) is subject...

  12. 40 CFR 721.520 - Alanine, N-(2-carboxyethyl)-N-alkyl-, salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-, salt. 721.520 Section 721.520 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.520 Alanine, N-(2-carboxyethyl)-N-alkyl-, salt. (a) Chemical substance... alanine, N-(2-carboxyethyl)-N- alkyl-, salt (P-89-336) is subject to reporting under this section for...

  13. 40 CFR 721.520 - Alanine, N-(2-carboxyethyl)-N-alkyl-, salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-, salt. 721.520 Section 721.520 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.520 Alanine, N-(2-carboxyethyl)-N-alkyl-, salt. (a) Chemical substance... alanine, N-(2-carboxyethyl)-N- alkyl-, salt (P-89-336) is subject to reporting under this section for...

  14. 40 CFR 721.520 - Alanine, N-(2-carboxyethyl)-N-alkyl-, salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-, salt. 721.520 Section 721.520 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.520 Alanine, N-(2-carboxyethyl)-N-alkyl-, salt. (a) Chemical substance... alanine, N-(2-carboxyethyl)-N- alkyl-, salt (P-89-336) is subject to reporting under this section for...

  15. Microbial Potential for Ecosystem N Loss Is Increased by Experimental N Deposition

    PubMed Central

    Upchurch, Rima A.; Zak, Donald R.

    2016-01-01

    Fossil fuel combustion and fertilizer use has increased the amount of biologically available N entering terrestrial ecosystems. Nonetheless, our understanding of how anthropogenic N may alter the physiological mechanisms by which soil microorganisms cycle N in soil is still developing. Here, we applied shotgun metagenomics to a replicated long-term field experiment to determine how two decades of experimental N deposition, at a rate expected by mid-century, has affected the genetic potential of the soil microbial community to cycle N in soils. Experimental N deposition lead to a significant and persistent increase in functional assemblages mediating N cycle transformations associated with ecosystem N loss (i.e., denitrification and nitrification), whereas functional assemblages associated with N input and retention (i.e., N fixation and microbial N assimilation) were less positively affected. Furthermore, the abundance and composition of microbial taxa, as well as functional assemblages involved in housekeeping functions (i.e., DNA replication) were unaffected by experimental N deposition. Taken together, our results suggest that functional genes and gene pathways associated with ecosystem N loss have been favored by experimental N deposition, which may represent a genetic mechanism fostering increased N loss as anthropogenic N deposition increases in the future. PMID:27737013

  16. 40 CFR 721.1085 - Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Benzenamine,4,4â²-methylenebis[N-ethyl-N-methyl-. 721.1085 Section 721.1085 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.1085 Benzenamine,4,4′-methylenebis[N-ethyl-N-methyl-. (a)...

  17. 40 CFR 721.225 - 2-Chloro-N-methyl-N-substituted acetamide (generic name).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false 2-Chloro-N-methyl-N-substituted... Specific Chemical Substances § 721.225 2-Chloro-N-methyl-N-substituted acetamide (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance...

  18. 40 CFR 721.4080 - MNNG (N-methyl-N′-nitro-N-nitrosoguanidine).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false MNNG (N-methyl-Nâ²-nitro-N... Specific Chemical Substances § 721.4080 MNNG (N-methyl-N′-nitro-N-nitrosoguanidine). (a) Chemical substance and significant new use subject to reporting. (1) The chemical substance MNNG...

  19. The chemical space of PbN-nBin and (PbN-nBin)(+): A systematic study for N = 3-13.

    PubMed

    Seifried, Christian; Longo, Lilla; Pollak, Patrik; Weigend, Florian

    2017-01-21

    A systematic exploration of the energy hypersurfaces of three to 13-atomic neutral and cationic binary lead-bismuth clusters is presented. Global minima for all 99 compositions (N = 3-13, n = 0-N) were obtained by a density functional theory based genetic algorithm, which was applied to every single composition, both for the neutral clusters and for the cations. Within the genetic algorithm, the energetically most favorable assignment of atom types to atom positions was found via aimed swapping of element types, based on first-order perturbation theory in the nuclear charge. Results of the genetic algorithm procedure were refined with high-level density functional treatments including also the effects of spin-orbit coupling. The resulting global minima were analyzed applying various stability criteria, finally yielding the ∼20 overall most stable neutral and cationic clusters in the chemical space of three to 13-atomic mixed lead bismuth clusters. In most cases, they are polyhedrons that obey the Wade-Mingos rules.

  20. The chemical space of PbN-nBin and (PbN-nBin)+: A systematic study for N = 3-13

    NASA Astrophysics Data System (ADS)

    Seifried, Christian; Longo, Lilla; Pollak, Patrik; Weigend, Florian

    2017-01-01

    A systematic exploration of the energy hypersurfaces of three to 13-atomic neutral and cationic binary lead-bismuth clusters is presented. Global minima for all 99 compositions (N = 3-13, n = 0-N) were obtained by a density functional theory based genetic algorithm, which was applied to every single composition, both for the neutral clusters and for the cations. Within the genetic algorithm, the energetically most favorable assignment of atom types to atom positions was found via aimed swapping of element types, based on first-order perturbation theory in the nuclear charge. Results of the genetic algorithm procedure were refined with high-level density functional treatments including also the effects of spin-orbit coupling. The resulting global minima were analyzed applying various stability criteria, finally yielding the ˜20 overall most stable neutral and cationic clusters in the chemical space of three to 13-atomic mixed lead bismuth clusters. In most cases, they are polyhedrons that obey the Wade-Mingos rules.

  1. 49 CFR Appendix - Figures to Subpart N of Part 572

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... Version Test conditions and instrumentation. Pt. 572, Subpt. N, Fig. N1 Figures to Subpart N of Part 572 ER18JY02.000 Pt. 572, Subpt. N, Fig. N2 ER18JY02.001 Pt. 572, Subpt. N, Fig. N3 ER18JY02.002 Pt. 572, Subpt. N, Fig. N4 ER13JA00.005 Pt. 572, Subpt. N, Fig. N5 ER19SE02.000 Pt. 572, Subpt. N, Fig. N6...

  2. 49 CFR Appendix - Figures to Subpart N of Part 572

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... Version Test conditions and instrumentation. Pt. 572, Subpt. N, Fig. N1 Figures to Subpart N of Part 572 ER18JY02.000 Pt. 572, Subpt. N, Fig. N2 ER18JY02.001 Pt. 572, Subpt. N, Fig. N3 ER18JY02.002 Pt. 572, Subpt. N, Fig. N4 ER13JA00.005 Pt. 572, Subpt. N, Fig. N5 ER19SE02.000 Pt. 572, Subpt. N, Fig. N6...

  3. 49 CFR Appendix - Figures to Subpart N of Part 572

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... Version Test conditions and instrumentation. Pt. 572, Subpt. N, Fig. N1 Figures to Subpart N of Part 572 ER18JY02.000 Pt. 572, Subpt. N, Fig. N2 ER18JY02.001 Pt. 572, Subpt. N, Fig. N3 ER18JY02.002 Pt. 572, Subpt. N, Fig. N4 ER13JA00.005 Pt. 572, Subpt. N, Fig. N5 ER19SE02.000 Pt. 572, Subpt. N, Fig. N6...

  4. 49 CFR Appendix - Figures to Subpart N of Part 572

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... Version Test conditions and instrumentation. Pt. 572, Subpt. N, Fig. N1 Figures to Subpart N of Part 572 ER18JY02.000 Pt. 572, Subpt. N, Fig. N2 ER18JY02.001 Pt. 572, Subpt. N, Fig. N3 ER18JY02.002 Pt. 572, Subpt. N, Fig. N4 ER13JA00.005 Pt. 572, Subpt. N, Fig. N5 ER19SE02.000 Pt. 572, Subpt. N, Fig. N6...

  5. An InN/InGaN/GaN nanowire array guided wave photodiode on silicon

    NASA Astrophysics Data System (ADS)

    Hazari, Arnab; Zunaid Baten, Md.; Yan, Lifan; Millunchick, Joanna M.; Bhattacharya, Pallab

    2016-11-01

    The III-nitride nanowire heterostructure arrays with multiple InN disk light absorbing regions have been grown by plasma-assisted molecular beam epitaxy on (001)Si substrates, and guided wave photodiodes have been fabricated and characterized. The spectral photocurrent of the devices has been measured under reverse bias, and the data exhibit distinct shoulders in the range of 0.69-3.2 eV (0.39-1.8 μm). The estimated responsivity at a wavelength of 1.3 μm is 0.2 A/W. The nanowire photodiode response was also measured with an excitation at one facet provided by an edge-emitting laser fabricated with the same nanowire array and emitting at 1.3 μm.

  6. Mössbauer investigation of FeTaN/TaN multilayer systems

    NASA Astrophysics Data System (ADS)

    Rogalski, M. S.; Amado, M. M.; Sousa, J. B.; Freitas, P. P.

    1999-05-01

    The microstructure of the [FeTaN(3200 Å)/TaN(50 Å)] n multilayer system, prepared by DC reactive magnetron sputtering, is studied by transmission and conversion electron Mössbauer spectroscopy, that indicate a predominant α-Fe texture and the presence of iron nitrides. Comparative phase analysis reveals formation of the paramagnetic nitride ɛ-Fe xN(2 < x < 3) in the interfacial region between the FeTaN and TaN spacer layers. This phase, whose relative fraction increases in proportion to the square of N 2 partial pressure during deposition, may account for the relatively large magnetostriction of the multilayer system.

  7. Two-step iron(0)-mediated N-demethylation of N-methyl alkaloids.

    PubMed

    Kok, Gaik B; Pye, Cory C; Singer, Robert D; Scammells, Peter J

    2010-07-16

    A mild and simple two-step Fe(0)-mediated N-demethylation of a number of tertiary N-methyl alkaloids is described. The tertiary N-methylamine is first oxidized to the corresponding N-oxide, which is isolated as the hydrochloride salt. Subsequent treatment of the N-oxide hydrochloride with iron powder readily provides the N-demethylated amine. Representative substrates include a number of opiate and tropane alkaloids. Key intermediates in the synthesis of semisynthetic 14-hydroxy pharmaceutical opiates such as oxycodone and oxymorphone are also readily N-demethylated using this method.

  8. Engineering of electric field distribution in GaN(cap)/AlGaN/GaN heterostructures: theoretical and experimental studies

    NASA Astrophysics Data System (ADS)

    Gladysiewicz, M.; Janicki, L.; Misiewicz, J.; Sobanska, M.; Klosek, K.; Zytkiewicz, Z. R.; Kudrawiec, R.

    2016-09-01

    Polarization engineering of GaN-based heterostructures opens a way to develop advanced transistor heterostructures, although measurement of the electric field in such heterostructures is not a simple task. In this work, contactless electroreflectance (CER) spectroscopy has been applied to measure the electric field in GaN-based heterostructures. For a set of GaN(d  =  0, 5, 15, and 30 nm)/AlGaN(20 nm)/GaN(buffer) heterostructures a decrease of electric field in the GaN(cap) layer from 0.66 MV cm-1 to 0.27 MV cm-1 and an increase of the electric field in the AlGaN layer from 0.57 MV cm-1 to 0.99 MV cm-1 have been observed with the increase in the GaN(cap) thickness from 5-30 nm. For a set of GaN(20 nm)/AlGaN(d  =  10, 20, 30, and 40 nm)/GaN(buffer) heterostructures a decrease of the electric field in the AlGaN layer from 1.77 MV cm-1 to 0.64 MV cm-1 and an increase of the electric field in the GaN layer from 0.57 MV cm-1 to 0.99 MV cm-1 were observed with the increase in the AlGaN thickness from 10-40 nm. To determine the distribution of the electric field in these heterostructures the Schrödinger and Poisson equations are solved in a self-consistent manner and matched with experimental data. It is shown that the built-in electric field in the GaN(cap) and AlGaN layers obtained from measurements does not reach values of electric field resulting only from polarization effects. The measured electric fields are smaller due to a screening of polarization effects by free carriers, which are inhomogeneously distributed across the heterostructure and accumulate at interfaces. The results clearly demonstrate that CER measurements supported by theoretical calculations are able to determine the electric field distribution in GaN-based heterostructures quantitatively, which is very important for polarization engineering in this material system.

  9. Elimination of AlGaN epilayer cracking by spatially patterned AlN mask

    NASA Astrophysics Data System (ADS)

    Sarzyński, Marcin; Kryśko, Marcin; Targowski, Grzegorz; Czernecki, Robert; Sarzyńska, Agnieszka; Libura, Adam; Krupczyński, Wiktor; Perlin, Piotr; Leszczyński, Michał

    2006-03-01

    The inherent problem in III-nitride technology is the cracking of AlGaN layers that results from lattice mismatch between AlGaN and GaN. In case of thin substrates (30-90μm), such as, bulk GaN grown by the high-pressure/high-temperature method, the bowing of AlGaN /GaN strained structures becomes an additional problem. To eliminate cracking and bowing, AlGaN layers were grown on GaN substrates with an AlN mask patterned to form 3-15μm wide windows. In the 3μm window, the AlGaN layer was not cracked, although its thickness and Al composition exceeded critical values for growth on nonpatterned substrates. Dislocation density in the windows was of 5×106/cm2.

  10. Internal quantum efficiency in yellow-amber light emitting AlGaN-InGaN-GaN heterostructures

    SciTech Connect

    Ngo, Thi Huong; Gil, Bernard; Valvin, Pierre; Damilano, Benjamin; Lekhal, Kaddour; De Mierry, Philippe

    2015-09-21

    We determine the internal quantum efficiency of strain-balanced AlGaN-InGaN-GaN hetero-structures designed for yellow-amber light emission, by using a recent model based on the kinetics of the photoluminescence decay initiated by Iwata et al. [J. Appl. Phys. 117, 075701 (2015)]. Our results indicate that low temperature internal quantum efficiencies sit in the 50% range and we measure that adding an AlGaN layer increases the internal quantum efficiency from 50% up to 57% with respect to the GaN-InGaN case. More dramatic, it almost doubles from 2.5% up to 4.3% at room temperature.

  11. Chloridobis(ethyl­enediamine-κ2 N,N′)(n-pentyl­amine-κN)cobalt(III) dichloride monhydrate

    PubMed Central

    Anbalagan, K.; Tamilselvan, M.; Nirmala, S.; Sudha, L.

    2009-01-01

    The title complex, [CoCl(C5H13N)(C2H8N2)2]Cl2·H2O, comprises one chloridobis(ethyl­enediamine)(n-pentyl­amine)cobalt(III) cation, two chloride counter-anions and a water mol­ecule. The CoIII atom of the complex is hexa­coordinated by five N and one Cl atoms. The five N atoms are from two chelating ethyl­enediamine and one n-pentyl­amine ligands. Neighbouring cations and anions are connected by N—H⋯Cl and N—H⋯O hydrogen bonds to each other and also to the water mol­ecule. PMID:21582753

  12. Recombination balance in green-light-emitting GaN/InGaN/AlGaN quantum wells

    NASA Astrophysics Data System (ADS)

    Eliseev, Petr G.; Osin'ski, Marek; Li, Hua; Akimova, Irina V.

    1999-12-01

    Recombination balance parameters for GaN/InGaN/AlGaN single-quantum-well green-lightemitting diodes are extracted from optical power and carrier lifetime measurements. The radiative recombination coefficient B is found to depend on two-dimensional carrier density N, with a low-carrier-density limit of B0=1.2×10-4 cm2/s. Sublinearity of the light-current characteristic at temperatures ⩾300 K is associated with a nonradiative process whose rate is proportional to ˜N4.8. The external quantum efficiency of 5.5% at 20 mA results from the internal quantum yield of 63% and the photon extraction efficiency of 8.7%. At low temperatures, a nonradiative loss term proportional to ˜N9 is also identified.

  13. Geometries and bond energies of GaH n and GaH n+ ( n=1-3)

    NASA Astrophysics Data System (ADS)

    Balasubramanian, K.

    1989-12-01

    Complete active space MCSCF (CASSCF) followed by full second-order configuration interaction (SOCI) calculations are carried out on the low-lying electronic states of GaH n and GaH n+ ( n=1-3). The equilibrium geometries of these species, bond energies D0(H n-1 Ga-H) and ionization potentials (IPs) of GaH n are calculated. The IPs of GaH n exhibit odd-even alternations. The ground state of GaH 2 is found to be bent while GaH 2+ is linear. The ground state of GaH 3 is found to be 1A 1 (triangular-planar) while that of GaH 3+ is a Jahn-Teller distorted 2B 2 (C 2v) state.

  14. Do Humans Really Learn A[superscript n] B[superscript n] Artificial Grammars from Exemplars?

    ERIC Educational Resources Information Center

    Hochmann, Jean-Remy; Azadpour, Mahan; Mehler, Jacques

    2008-01-01

    An important topic in the evolution of language is the kinds of grammars that can be computed by humans and other animals. Fitch and Hauser (F&H; 2004) approached this question by assessing the ability of different species to learn 2 grammars, (AB)[superscript n] and A[superscript n] B[superscript n]. A[superscript n] B[superscript n] was taken to…

  15. Arctocypris fuhrmanni, n. gen., n. sp. (Crustacea, Ostracoda, Eucypridinae) from Spitsbergen (Norway).

    PubMed

    Petkovski, Trajan K; Scharf, Burkhard; Keyser, Dietmar

    2016-01-14

    Material from Spitsbergen (Norway) collected by Spitzenberger (1996) was reinvestigated. A new genus Arctocypris and a new species Arctocypris. fuhrmanni n. gen. n. sp. are described in the present paper. A key to the genera of the subfamily Eucypridinae is provided. At the moment Arctocypris n. gen. comprises four species: Arctocypris arctica (Olofsson, 1918) comb. nov.; A. dulcifons (Diebel & Pietrzeniuk, 1969) comb. nov.; A. foveata (Delorme, 1968) comb. nov. and Arctocypris fuhrmanni n. gen., n. sp.

  16. Investigation of the electrical properties of nCdS-nGaAs heterostructures

    NASA Astrophysics Data System (ADS)

    Akramov, Kh. T.; Aripov, K. Sh.; Teshabaev, A. T.

    An investigation is made of barrier formation in nCdS-nGaAs heterostructures based on n(+)-n GaAs structures and nGaAs single crystals. Attention is given to: (1) the dark volt-ampere characteristics at temperatures ranging from 77 to 300 K; (2) the C-V characteristics at room temperature and liquid-nitrogen temperature; and (3) the frequency dependence of capacitance at 300 K.

  17. Soil N and 15N variation with time in a California annual grassland ecosystem

    USGS Publications Warehouse

    Brenner, D.L.; Amundson, Ronald; Baisden, W. Troy; Kendall, C.; Harden, J.

    2001-01-01

    The %N and ??15N values of soils and plants were measured along a chronosequence spanning 3 to 3000 Ky in a California annual grassland. Total soil N decreased with increasing soil age (1.1 to 0.4 kg N m-2) while the mean ?? 15N values of the soil N increased by several ??? from the youngest to oldest sites (+3.5 to +6.2 ???). The ?? 15N values of plants varied along the gradient, reflecting changing soil N pools and differences in the form of N uptake. The decline in total N storage with time is hypothesized to be due to a shift from N to P limitation with increasing soil age. The general increase in ?? 15N values with time is interpreted using a N mass balance model, and appears to reflect a shift toward an increasing proportional losses of inorganic mineral forms of N (vs. organic forms) with increasing soil age. We develop a quantitative index of this trend (mineral vs. organic forms of N loss) using mass balance considerations and parameters. The %N and ?? 15N values along the California age gradient were compared to the published data for a comparably aged chronosequence in Hawaii. Most striking in this comparison is the observation that the California soil and plant ?? 15N values are several ??? greater than those on comparably aged Hawaiian sites. Multiple explanations are plausible, but assuming the sites have a similar range in ?? 15N values of atmospheric inputs, the isotopic differences suggest that N may be, at least seasonally, in greater excess in the strongly seasonal, semi-arid, California grassland. Copyright ?? 2001 Elsevier Science Ltd.

  18. Development of GaN/AlGaN Terahertz Quantum Cascade Laser

    DTIC Science & Technology

    2008-11-19

    AFOSR-Taiwan Nanoscience Initiative Project Final Report Project Title Development of GaN /AlGaN Terahertz Quantum Cascade Laser...DATES COVERED 14-06-2007 to 13-06-2008 4. TITLE AND SUBTITLE Development of GaN -Based Terahertz Quantum Cascade Laser 5a. CONTRACT NUMBER...the GaN /AlGaN active region for terahertz quantum cascade lasers using MOCVD system based on the quantum cascade structure proposed by Prof. Greg Sun

  19. The Crystal Structures of Mg 3N 2and Zn 3N 2

    NASA Astrophysics Data System (ADS)

    Partin, D. E.; Williams, D. J.; O'Keeffe, M.

    1997-08-01

    The structures of Mg3N2and Zn3N2have been refined from neutron time-of-flight powder diffraction data. These compounds have the antibixbyite structure and are the first such to be fully refined. The space group isIaoverline3,a=9.9528(1) Å (Mg3N2) and 9.7691(1) Å (Zn3N2). A revised bond valence parameter for Mg-N bonds is suggested.

  20. Primes in Fibonacci n-step and Lucas n-step Sequences

    NASA Astrophysics Data System (ADS)

    Noe, Tony D.; Vos Post, Jonathan

    2005-09-01

    We search for primes in the Fibonacci n-step and Lucas n-step sequences, which are the natural generalizations of the Fibonacci and Lucas numbers. While the Fibonacci n-step sequences are nearly devoid of primes, the Lucas n-step sequences are prime-rich. We tabulate the occurrence of primes in the first 10000 terms for n <= 100. We also state two conjectures about Diophantine equations based on these sequences.

  1. 40 CFR 721.3152 - Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates (salts). 721.3152 Section 721... Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates... ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

  2. 40 CFR 721.3152 - Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates (salts). 721.3152 Section 721... Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates... ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

  3. 40 CFR 721.3152 - Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates (salts). 721.3152 Section 721... Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates... ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

  4. 40 CFR 721.3152 - Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates (salts). 721.3152 Section 721... Ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl sulfates... ethanaminium, N-ethyl-2-hydroxy-N,N-bis(2-hydroxyethyl)-, diester with C12-18 fatty acids, ethyl...

  5. Process dependency on threshold voltage of GaN MOSFET on AlGaN/GaN heterostructure

    NASA Astrophysics Data System (ADS)

    Wang, Qingpeng; Jiang, Ying; Miyashita, Takahiro; Motoyama, Shin-ichi; Li, Liuan; Wang, Dejun; Ohno, Yasuo; Ao, Jin-Ping

    2014-09-01

    GaN metal-oxide-semiconductor field-effect transistors (MOSFETs) with recessed gate on AlGaN/GaN heterostructure are reported in which the drain and source ohmic contacts were fabricated on the AlGaN/GaN heterostructure and the electron channel was formed on the GaN buffer layer by removing the AlGaN barrier layer. Negative threshold voltages were commonly observed in all devices. To investigate the reasons of the negative threshold voltages, different oxide thickness, etching gas and bias power of inductively-coupled plasma (ICP) system were utilized in the fabrication process of the GaN MOSFETs. It is found that positive charges of around 1 × 1012 q/cm2 exist near the interface at the just threshold condition in both silane- and tetraethylorthosilicate (TEOS)-based devices. It is also found that the threshold voltages do not obviously change with the different etching gas (SiCl4, BCl3 and two-step etching of SiCl4/Cl2) at the same ICP bias power level (20-25 W) and will become deeper when higher bias power is used in the dry recess process which may be related to the much serious ion bombardment damage. Furthermore, X-ray photoelectron spectroscopy (XPS) experiments were done to investigate the surface conditions. It is found that N 1s peaks become lower with higher bias power of the dry etching process. Also, silicon contamination was found and could be removed by HNO3/HF solution. It indicates that the nitrogen vacancies are mainly responsible for the negative threshold voltages rather than the silicon contamination. It demonstrates that optimization of the ICP recess conditions and improvement of the surface condition are still necessary to realize enhancement-mode GaN MOSFETs on AlGaN/GaN heterostructure.

  6. Induction of esophageal cancer associated with gastric cancer in a dog by N-ethyl-N'-nitro-N-nitrosoguandine.

    PubMed

    Sekizuka, H; Doi, H; Sunagawa, M; Nagai, S; Kojima, S

    1975-12-01

    The experimental induction of gastric cancer was studied in four dogs given oral administration of N-ethyl-N'-nitro-N-nitrosoguanidine (ENNG) in solution. Esophageal cancer with the regional lymph node metastasis was found in one dog at autopsy, with concomitantly existing gastric cancer. This dog, which ingested a total amount of about 38 g of ENNG, died of weakness on the 513th experimental day. Three remaining dogs are still living and under observation.

  7. Impact of AlN Spacer on Analog Performance of Lattice-Matched AlInN/AlN/GaN MOSHEMT

    NASA Astrophysics Data System (ADS)

    Jena, Kanjalochan; Swain, Raghunandan; Lenka, T. R.

    2016-04-01

    In this work, a detailed investigation of the impact of spacer layer thickness on analog performance of an AlInN/AlN/GaN metal oxide semiconductor high electron mobility transistor (MOSHEMT) is carried out. A thorough analysis of the key figure-of-merits such as threshold voltage (V th), two-dimensional electron gas sheet charge density (n s), drain current (I d), transconductance (g m), and gate leakage current are performed for various spacer thicknesses ranging from 0.5 nm to 1.8 nm. From the two-dimensional ATLAS device simulation results, it is observed that the performance of AlInN/AlN/GaN MOSHEMT is affected by the variation of spacer thickness. Also, we have developed mathematical expressions for the evaluation of V th , n s , I d , g m and gate leakage current for the proposed device. The model results and technology computer-aided design simulation results are verified and also found to be satisfactory. Improved sheet charge density and superior analog performance is observed due to the insertion of the AlN spacer. Suppression in the forward gate current is observed due to the insertion of the AlN spacer which made it possible to apply a high gate voltage in the transistor operation. From the fabrication point of view, it is also feasible to utilize the existing complementary metal-oxide-semiconductor process flows to fabricate the proposed device.

  8. Does elevated N make lignin more recalcitrant?

    NASA Astrophysics Data System (ADS)

    Weintraub, M. N.; Rinkes, Z. L.; Grandy, S.; Wickings, K.; Bertrand, I.

    2014-12-01

    Increases in nitrogen (N) availability are often found to reduce decomposition rates of lignin-rich plant litter. However, the biological and chemical mechanisms that cause this inhibitory effect are still unclear. Our goal was to determine why increased N availability inhibits lignin decomposition. We tested two competing hypotheses: 1) decomposers degrade lignin to obtain protected N compounds and stop producing lignin-degrading enzymes if mineral N is available; or 2) chemical reactions between lignin and mineral N make lignin more recalcitrant, thereby limiting the ability of decomposers to break it down. To test these hypotheses, we followed changes in carbon (C) mineralization, microbial biomass and enzyme activities, litter chemistry, and lignin monomer concentrations over a 478-day laboratory incubation of three genotypes of maize stem internodes varying in litter quality. They were factorially combined with either an acidic or neutral pH sandy soil, with and without added N. Adding N reduced C mineralization, microbial biomass, and lignin-degrading enzyme activities in all treatments. Furthermore, our data on litter chemistry and lignin monomers indicate that N addition did not significantly alter the quantity or quality of lignin in any treatment. These results suggest that abiotic interactions between N and lignin compounds did not alter the ability of decomposers to breakdown lignin. Thus, we conclude that mineral N alters microbial enzyme and biomass dynamics, but not lignin chemistry during maize decomposition.

  9. N-acetylgalactosaminyltransferases in cancer

    PubMed Central

    Hussain, Muhammad Ramzan Manwar; Hoessli, Daniel C.; Fang, Min

    2016-01-01

    Aberrant mucin-type O-glycosylation by glycosyltransferases is a well-described hallmark of many cancers and is also associated with additional non-cancerous developmental and metabolic disorders. The current review focuses on N-acetylgalactosaminyltransferase genes (GALNTs) and proteins (GalNAcTs) to illustrate their importance in cancer biology. Aberrant O-glycosylation by GalNAcTs activates a wide range of proteins that carry out interactions of sessile and motile cells affecting organogenesis, responses to agonists and stimulating hyperproliferation and metastatisation of neoplastic cells. As genome-wide analyses have provided abundant clues regarding under- or over-expressed genes that characterize different types of cancers, GALNTs and their transferase products have attracted attention by being unexpected actors in neoplastic contexts. We intend to review the current knowledge on GALNTs and their encoded transferases in cancer and suggest what could be the significance of such information in cancer pathogenesis and management. PMID:27322213

  10. Effect of buffer structures on AlGaN/GaN high electron mobility transistor reliability

    SciTech Connect

    Liu, L.; Xi, Y. Y.; Ren, F.; Pearton, S. J.; Laboutin, O.; Cao, Yu; Johnson, Wayne J.; Kravchenko, Ivan I

    2012-01-01

    AlGaN/GaN high electron mobility transistors (HEMTs) with three different types of buffer layers, including a GaN/AlGaN composite layer, or 1 or 2 lm GaN thick layers, were fabricated and their reliability compared. The HEMTs with the thick GaN buffer layer showed the lowest critical voltage (Vcri) during off-state drain step-stress, but this was increased by around 50% and 100% for devices with the composite AlGaN/GaN buffer layers or thinner GaN buffers, respectively. The Voff - state for HEMTs with thin GaN and composite buffers were 100 V, however, this degraded to 50 60V for devices with thick GaN buffers due to the difference in peak electric field near the gate edge. A similar trend was observed in the isolation breakdown voltage measurements, with the highest Viso achieved based on thin GaN or composite buffer designs (600 700 V), while a much smaller Viso of 200V was measured on HEMTs with the thick GaN buffer layers. These results demonstrate the strong influence of buffer structure and defect density on AlGaN/GaN HEMT performance and reliability.

  11. Microwave transitions from pairs of Rb n d5 /2n d5 /2 atoms

    NASA Astrophysics Data System (ADS)

    Lee, Jeonghun; Gallagher, T. F.

    2016-06-01

    We have observed resonant microwave transitions between pairs of atoms. Specifically, we have observed the processes n d5 /2n d5 /2→(n +1 ) dj(n -2 ) f7 /2 and n d5 /2n d5 /2→(n +2 ) p3 /2(n -1 ) d5 /2 for 35 ≤n ≤44 . These transitions are allowed due to the dipole-dipole-induced configuration interaction between the n d5 /2n d5 /2 state and the energetically nearby (n +2 ) p3 /2(n -2 ) f7 /2 state, which admixes some of the latter into the former. The resulting microwave transitions are analogous to two-photon transitions in which one of the photons has been replaced by the dipole-dipole interaction. We have developed a configuration interaction description of the transitions, which gives a good description of the interaction over the range 35 ≤n ≤42 . Over this range of n the detuning varies from 0.095 to 1.482 GHz, the microwave frequencies vary from 26.970 to 45.916 GHz, and the requisite microwave powers vary by a factor of over 1000.

  12. Efficient carrier relaxation and fast carrier recombination of N-polar InGaN/GaN light emitting diodes

    SciTech Connect

    Feng, Shih-Wei Liao, Po-Hsun; Leung, Benjamin; Han, Jung; Yang, Fann-Wei; Wang, Hsiang-Chen

    2015-07-28

    Based on quantum efficiency and time-resolved electroluminescence measurements, the effects of carrier localization and quantum-confined Stark effect (QCSE) on carrier transport and recombination dynamics of Ga- and N-polar InGaN/GaN light-emitting diodes (LEDs) are reported. The N-polar LED exhibits shorter ns-scale response, rising, delay, and recombination times than the Ga-polar one does. Stronger carrier localization and the combined effects of suppressed QCSE and electric field and lower potential barrier acting upon the forward bias in an N-polar LED provide the advantages of more efficient carrier relaxation and faster carrier recombination. By optimizing growth conditions to enhance the radiative recombination, the advantages of more efficient carrier relaxation and faster carrier recombination in a competitive performance N-polar LED can be realized for applications of high-speed flash LEDs. The research results provide important information for carrier transport and recombination dynamics of an N-polar InGaN/GaN LED.

  13. Tuning emission in violet, blue, green and red in cubic GaN/InGaN/GaN quantum wells

    NASA Astrophysics Data System (ADS)

    Orozco Hinostroza, I. E.; Avalos-Borja, M.; Compeán García, V. D.; Zamora, C. Cuellar; Rodríguez, A. G.; López Luna, E.; Vidal, M. A.

    2016-02-01

    Light emission in the three primary colors was achieved in cubic GaN/InGaN/GaN heterostructures grown by molecular beam epitaxy on MgO substrates in a single growth process. A heterostructure with four quantum wells with a width of 10 nm was grown; this quantum wells width decrease the segregation effect of In. Photoluminescence emission produced four different emission signals: violet, blue, green-yellow and red. Thus, we were able to tune energy transitions in the visible spectrum modifying the In concentration in cubic InxGa1-xN ternary alloy.

  14. Analytical modeling of AlGaN/AlN/GaN heterostructures including effects of distributed surface donor states

    SciTech Connect

    Goyal, Nitin; Fjeldly, Tor A.

    2014-07-14

    In this paper, a physics based analytical model is presented for calculation of the two-dimensional electron gas density and the bare surface barrier height of AlGaN/AlN/GaN material stacks. The presented model is based on the concept of distributed surface donor states and the self-consistent solution of Poisson equation at the different material interfaces. The model shows good agreement with the reported experimental data and can be used for the design and characterization of advanced GaN devices for power and radio frequency applications.

  15. Luminescence Properties of GaN:Tb, GaN/AlGaN:Eu Superlattice, and AlN:Tb and Eu.

    NASA Astrophysics Data System (ADS)

    Lozykowski, H. J.; Jadwisienczak, W. M.; Brown, I. G.

    2001-03-01

    We report on recent progress in the investigation of cathodoluminescence (CL) of GaN doped with Tb, the visible photoluminescence (PL) and CL of GaN and Al_0.14Ga_0.86N /GaN superlattice doped with Eu, and the CL from AlN doped with Eu and Tb. The CL of GaN:Tb shows sharp emission lines corresponding to Tb^3+ ions transitions resolved in the spectral range from 350 nm to 750 nm, and observed over the temperature range of 7 - 330 K. The luminescence exhibits transitions which originate in the ^5D3 and ^5D4 levels and terminate in the ^7F manifolds. The depth resolved CL spectra analysis show a luminescence surface dead layer thickness of ~20 nm. The decay times for ^5D_3-->^7F5 (423.4nm) and ^5D_4-->^7F5 (551.6nm) transitions at 7 K are ~0.7 and ~1.8 ms, with little change with temperature. The visible PL and CL of GaN and Al_0.14Ga_0.86N/GaN superlattice doped with Eu ions, show sharp characteristic emission lines corresponding to Eu^3+ intra-4f^6-shell transitions. The luminescence shows dominant ^5D_0-->^7F_1,2,3 and weaker ^5D_0-->^7F_4,5,6 and ^5D_1-->^7F1 transitions. The intensity of Eu emission from Al_0.14Ga_0.86N/GaN superlattice annealed in N2 is ~58% stronger than from Eu in the GaN epilayer. Strong CL was observed from AlN thin single crystal films doped with Eu^3+ and Tb^3+ ions. The space group symmetry of the wurtzite AlN is C-P6_3mc and the Al cation occupies the site of point group symmetry C_3v. We assume that those implanted RE ions in AlN occupy relaxed substitutional Al-sites with hexagonal C_3v crystal symmetry. Emission lines corresponding to Eu^3+ and Tb^3+ intra-4f^n-shell transitions are resolved in the spectral range from 300 to 900 nm. The CL kinetics for several transitions of Eu^3+ (^5D_0), Tb^3+ (^5D_3,4) were analyzed. (Electronic mail: lozykows/@bobcat.ent.ohiou.edu)

  16. Transport imaging for contact-free measurements of minority carrier diffusion in GaN, GaN/AlGaN, and GaN/InGaN core-shell nanowires

    SciTech Connect

    Baird, Lee; Ong, C. P.; Cole, R. Adam; Haegel, N. M.; Talin, A. Alec; Li, Qiming; Wang, George T.

    2011-03-28

    Minority carrier diffusion lengths Ld are calculated for GaN, GaN/AlGaN, and GaN/InGaN core-shell nanowires using a procedure based on imaging of recombination luminescence. The result of shell material on conveyance properties is recorded. An AlGaN shell produces Ld values in surplus of 1μm and a relative insensitivity to wire diameter. An InGaN shell reduces effective diffusion length, while a dependence of Ld on diameter is observed for unshielded nanowires.

  17. High N2O emission in an N-saturated subtropical forest, southwest China

    NASA Astrophysics Data System (ADS)

    Dörsch, P.; Zhu, J.; Mulder, J.

    2012-04-01

    Nitrogen (N)-saturated forests in subtropical China are significant N sinks, despite low forest growth rates. In a forested headwater catchment at Tieshanping, Chongqing, SW China, with 4 g N m-2a-1 atmogenic deposition (60% of which as NH4+-N) and leaching of only 0.6 g N m-2 a-1 (NO3--N dominated), we applied state-of-the-art field and laboratory methodologies to investigate the nature of the N sinks. The study included the determination of spatiotemporal patterns of N2O emission, a 15N labeling experiment and laboratory incubations to determine nitrification and denitrification characteristics and their gaseous product stoichiometries. Emission of N2O occurred predominantly during the wet season (summer), driven by rain episodes. N2O emission rates were particularly high along a hill slope (HS) with a thin organic surface layer overlaying an argic B horizon causing transient interflow during storm flow conditions. Lower N2O emission rates were observed at the foot slope in a colluvium-derived groundwater discharge zone (GDZ). Laboratory incubation experiments suggested that the difference in N2O emission rate is primarily due to higher N2O/N2 product ratios of denitrification in the HS topsoil being exposed to frequent drying-rewetting. Lower N2O/N2 product ratios in soils of the GDZ, in turn, could be attributed to more stable anoxia, lower NO3- availability and higher pH as compared with the hillslope, all of which favor the expression of N2O reductase. Estimated annual N2O emission for the relatively dry hydrological year 2009-2010 was 0.4 g N m-2, which is equivalent to approximately 10% of the annual input of reactive N. Measurements during summer 2009 indicated that N2O emissions can be even higher during wet years. A 15NO3- labeling experiment conducted on HS soils during summer revealed that between 75 and 86% of the N2O emission derived from denitrification during the first 6 days after label addition, accounting for 8-15% of the applied NO3--N. Our

  18. Mechanism of N2 dissociation and kinetics of N(4S) atoms in pure nitrogen plasma

    NASA Astrophysics Data System (ADS)

    Volynets, A. V.; Lopaev, D. V.; Popov, N. A.

    2016-10-01

    This work deals with kinetics of the ground state nitrogen atoms N(4S) and N2 dissociation mechanism in pure nitrogen plasma. The experiment was carried out in positive column of DC glow discharge at a range of parameters p = 5 - 50 Torr, J = 20 - 100 mA. The use of axial homogeneous glow discharge allowed considering N(4S) balance for spatially uniform conditions controlled by only two terms: source (characterized by effective production rate k diss eff ) and loss (characterized by effective loss time τN l oss ). Analysis of these parameters gains considerably better understanding of N2 dissociation mechanism in pure nitrogen plasma that was the main goal of the given work. So N/N2 dissociation rate as function of discharge parameters was obtained using two independent emission optical methods: actinometry on Ar atoms and N2 2+ band emission decay at discharge modulation. Measurements of N/N2 radial profiles allowed estimating N atom surface loss probability γN l oss and correspondingly τN l oss . It was revealed that γN l oss depends on N(4S) concentration and thereby discharge conditions through the sorption balance of physisorbed N atoms. Simple phenomenological model taking into account basic surface processes provides γN l oss data in good agreement with experiment. Finally, k diss eff was obtained as function of reduced electric field E/N and it was shown that even EEDF self-consistently calculated with accounting for N2 vibrational excitation is unable to provide observed values of k diss eff . Reasons of that fact are discussed in detail.

  19. Luminescent complexes of iridium(III) containing N/\\C/\\N-coordinating terdentate ligands.

    PubMed

    Wilkinson, Andrew J; Puschmann, Horst; Howard, Judith A K; Foster, Clive E; Williams, J A Gareth

    2006-10-16

    A family of bis-terdentate iridium(III) complexes is reported which contain a cyclometalated, N/\\C[wedge]N-coordinating 1,3-di(2-pyridyl)benzene derivative. This coordination mode is favored by blocking competitive cyclometalation at the C4 and C6 positions of the ligand. Thus, 1,3-di(2-pyridyl)-4,6-dimethylbenzene (dpyxH) reacts with IrCl3 x 3H2O to generate a dichlorobridged dimer [Ir(dpyx-N,C,N)Cl(mu-Cl)]2, 1. This dimer is cleaved by DMSO to give [Ir(dpyx)(DMSO)Cl2], the X-ray crystal structure of which is reported here, confirming the N/\\C/\\N coordination mode of dpyx. The dimer 1 can also be cleaved by a variety of other ligands to generate novel classes of mononuclear complexes. These include charge-neutral bis-terdentate complexes of the form [Ir(N/\\C/\\N)(C/\\N/\\C)] and [Ir(N/\\C/\\N)(C/\\N/\\O)], by reaction of 1 with C/\\N/\\C-coordinating ligands (e.g., 2,6-diphenylpyridine and derivatives) and C/\\N/\\O-coordinating ligands (based on 6-phenylpicolinate), respectively. Treatment of 1 with terpyridines leads to dicationic complexes of the type [Ir(N/\\C/\\N)(N/\\N/\\N)]2+, while 2-phenylpyridine gives [Ir(dpyx-N/\\C/\\N)(ppy-C,N)Cl]. All of the charge-neutral complexes are luminescent in fluid solution at room temperature. Assignment of the emission to charge-transfer excited states with significant MLCT character is supported by DFT calculations. In the [Ir(N/\\C/\\N)(C/\\N/\\C)] class, fluorination of the C/\\N/\\C ligand at the phenyl 2' and 4' positions leads to a blue-shift in the emission and to an increase in the quantum yield (lambda(max) = 547 nm, phi = 0.41 in degassed CH(3)CN at 295 K) compared to the nonfluorinated parent complex (lambda(max) = 585 nm, phi = 0.21), as well as to a stabilization of the compound with respect to photodissociation through cleavage of mutually trans Ir-C bonds. [Ir(dpyx-N/\\C/\\N)(ppy-C,N)Cl] is an exceptionally bright emitter: phi = 0.76, lambda(max) = 508 nm, in CH(3)CN at 295 K. In contrast, the [Ir(N/\\C/\\N)(C/\\N

  20. New series of Tc-99m-labeled hepatobiliary tracers: N'-acyl- and N'-sulfonyl ethylenediamine-N,N-diacetic acids

    SciTech Connect

    Karube, Y.; Kono, A.; Maeda, T.; Ohya, M.; Matsushima, Y.

    1981-07-01

    Various Tc-99m-labeled N'-substituted derivatives of ethylenediamine-N,N-diacetic acid (EDDA) are evaluated as hepatobiliary imaging agents. N'-substituted aromatic acyl and aromatic sulfonyl derivatives of EDDA, labeled with Tc-99m, were administered to rabbits and golden hamsters, and the distribution indicated clearance by the hepatobiliary system. N'-aromatic sulfonyl EDDAs were labeled with Tc-99m by the SnCl/sub 2/ method with more than 99% yield. Clearance of Tc-99m-p-toluenesulfonyl EDDA from the blood and the liver was as rapid as that of Tc-99m N-(2,6-diethylphenylcarbamoylmethyl)iminodiacetic acid (Tc-99m diethyl IDA). Substitution of a bulky group at the aromatic ring in Tc-99m benzene-sulfonyl EDDA lowered urinary excretion. It is concluded that the sulfonyl EDDAs provide a fruitful source for Tc-99m-labeled hepatobiliary radiopharmaceuticals.

  1. New series of Tc-99m-labeled hepatobiliary tracers: N'-acyl- and N'-sulfonyl ethylenediamine-N,N-diacetic acids

    SciTech Connect

    Karube, Y.; Kono, A.; Maeda, T.; Ohya, M.; Matsushima, Y.

    1981-07-01

    Various Tc-99m-labeled N'-substituted derivatives of ethylenediamine-N,N-diacetic acid (EDDA) are evaluated as hepatobiliary imaging agents. N-substituted aromatic acyl and aromatic sulfonyl derivatives of EDDA, labeled with Tc-99m, were administered to rabbits and golden hamsters, and the distribution indicated clearance by the hepatobiliary system. N'-aromatic sulfonyl EDDAs were labeled with Tc-99m by the SnCl/sub 2/ method with more than 99% yield. Clearance of Tc-99m-p-toluenesulfonyl EDDA from the blood and the liver was as rapid as that of TC-99m N-(2,6-diethylphenylcarbamoylmethyl)iminodiacetic acid (Tc-99m benzenesulfonyl EDDA lowered urinary excretion. It is concluded that the sulfonyl EDDAs provide a fruitful source for Tc-99m-labeled hepatobiliary radiopharmaceuticals.

  2. Some properties of n-dimensional triangulations

    NASA Technical Reports Server (NTRS)

    Lawson, C. L.

    1985-01-01

    A number of mathematical results relevant to the problem of constructing a triangulation, i.e., a simplicial tessellation, of the convex hull of an arbitrary finite set of points in n-space are described. The principal results achieved are: (1) a set of n+2 points in n-space may be triangulated in at most 2 different ways; (2) the sphere test defined in this report selects a preferred one of these two triangulations; (3) a set of parameters is defined that permits the characterization and enumeration of all sets of n+2 points in n-space that are significantly different from the point of view of their possible triangulation; (4) the local sphere test induces a global sphere test property for a triangulation; and (5) a triangulation satisfying the global sphere property is dual to the n-dimensional Dirichlet tesselation, i.e., it is a Delaunay triangulation.

  3. InGaN-BASED Laser Diodes

    NASA Astrophysics Data System (ADS)

    Nakamura, Shuji

    1998-08-01

    Continuous-wave operation of InGaN multi-quantum-well (MQW) structure laser diodes (LDs) has been demonstrated at room temperature with output power up to 50 mW, operating temperature up to 100oC, emission wavelength of 400-420 nm, and a lifetime up to 300 h. InGaN MQW LDs with a lifetime of more than 1000 h are expected soon. Commercialization will begin in 1998 if research on the bluish-purple InGaN-based laser diodes continues to progress. The stimulated emission of the InGaN-based LDs originates from localized energy states of 100-250 meV depth, which are equivalent to quantum dot energy states, probably arising from from InGaN composition fluctuation in the InGaN well layers.

  4. Nilpotent deformations of N = 2 superspace

    NASA Astrophysics Data System (ADS)

    Ivanov, Evgeny; Zupnik, Boris; Lechtenfeld, Olaf

    2004-02-01

    We investigate deformations of four-dimensional N = (1,1) euclidean superspace induced by nonanticommuting fermionic coordinates. We essentially use the harmonic superspace approach and consider nilpotent bi-differential Poisson operators only. One variant of such deformations (termed chiral nilpotent) directly generalizes the recently studied chiral deformation of N = (1/2,1/2) superspace. It preserves chirality and harmonic analyticity but generically breaks N = (1,1) to N = (1,0) supersymmetry. Yet, for degenerate choices of the constant deformation matrix N = (1,1/2) supersymmetry can be retained, i.e. a fraction of 3/4. An alternative version (termed analytic nilpotent) imposes minimal nonanticommutativity on the analytic coordinates of harmonic superspace. It does not affect the analytic subspace and respects all supersymmetries, at the expense of chirality however. For a chiral nilpotent deformation, we present non(anti)commutative euclidean analogs of N = 2 Maxwell and hypermultiplet off-shell actions.

  5. Pd/GaN(0001) interface properties

    NASA Astrophysics Data System (ADS)

    Grodzicki, M.; Mazur, P.; Zuber, S.; Pers, J.; Ciszewski, A.

    2014-06-01

    This report concerns the properties of an interface formed between Pd films deposited onto the surface of (0001)-oriented n-type GaN at room temperature (RT) under ultrahigh vacuum. The surface of clean substrate and the stages of Pd-film growth were characterized in situ by X-ray photoelectron spectroscopy (XPS), scanning tunneling microscopy (STM), ultraviolet photoelectron spectroscopy (UPS), and low energy electron diffraction (LEED). As-deposited Pd films are grainy, cover the substrate surface uniformly and reproduce its topography. Electron affinity of the clean n-GaN surface amounts to 3.1 eV. The work function of the Pd-film is equal to 5.3 eV. No chemical interaction has been found at the Pd/GaN interface formed at RT. The Schottky barrier height of the Pd/GaN contact is equal to 1.60 eV.

  6. Territory covered by N random walkers.

    PubMed

    Yuste, S B; Acedo, L

    1999-10-01

    The problem of evaluating the number of distinct sites S(N)(t) covered up to time t by N random walkers is revisited. For the nontrivial time regime and for N>1 we show how to get the asymptotic behavior of S(N)(t) and we calculate the main and first two corrective terms. The mth corrective term decays mildly as 1/ln(m) N. For d-dimensional (d=1,2,3) simple cubic lattices, the main term is the volume of the hypersphere of radius [(ln N(2))2Dt/d](1/2), D being the diffusion constant, and the corrective terms account for the roughening of the surface of the set of visited sites.

  7. Asymmetric quantum-well structures for AlGaN/GaN/AlGaN resonant tunneling diodes

    NASA Astrophysics Data System (ADS)

    Yang, Lin'an; Li, Yue; Wang, Ying; Xu, Shengrui; Hao, Yue

    2016-04-01

    Asymmetric quantum-well (QW) structures including the asymmetric potential-barrier and the asymmetric potential-well are proposed for AlGaN/GaN/AlGaN resonant tunneling diodes (RTDs). Theoretical investigation gives that an appropriate decrease in Al composition and thickness for emitter barrier as well as an appropriate increase of both for collector barrier can evidently improve the negative-differential-resistance characteristic of RTD. Numerical simulation shows that RTD with a 1.5-nm-thick GaN well sandwiched by a 1.3-nm-thick Al0.15Ga0.85N emitter barrier and a 1.7-nm-thick Al0.25Ga0.75N collector barrier can yield the I-V characteristic having the peak current (Ip) and the peak-to-valley current ratio (PVCR) of 0.39 A and 3.6, respectively, about double that of RTD with a 1.5-nm-thick Al0.2Ga0.8N for both barriers. It is also found that an introduction of InGaN sub-QW into the diode can change the tunneling mode and achieve higher transmission coefficient of electron. The simulation demonstrates that RTD with a 2.8-nm-thick In0.03Ga0.97N sub-well in front of a 2.0-nm-thick GaN main-well can exhibit the I-V characteristic having Ip and PVCR of 0.07 A and 11.6, about 7 times and double the value of RTD without sub-QW, respectively. The purpose of improving the structure of GaN-based QW is to solve apparent contradiction between the device structure and the device manufacturability of new generation RTDs for sub-millimeter and terahertz applications.

  8. Surface potential measurements on GaN and AlGaN/GaN heterostructures by scanning Kelvin probe microscopy

    SciTech Connect

    Koley, G.; Spencer, M. G.

    2001-07-01

    Surface potentials on GaN epilayers and Al{sub 0.35}Ga{sub 0.65}N/GaN heterostructures have been studied by scanning Kelvin probe microscopy (SKPM) in conjunction with noncontact atomic force microscopy. The dependence of the surface potential on doping in GaN films, as well as the variation of surface potential with Al{sub 0.35}Ga{sub 0.65}N barrier layer thickness has been investigated. The bare surface barrier height (BSBH), as measured by SKPM, is observed to decrease from {similar_to}1. 40{+-}0.1 eV to {similar_to}0.60{+-}0.1 eV with increasing doping in the GaN epilayers. Schottky barrier height calculated from the measurements of BSBH on n-GaN agrees very well with results from previous studies. We have also estimated the surface state density for GaN based on the measured values of BSBH. The semiconductor {open_quotes}work function{close_quotes} at the Al{sub 0.35}Ga{sub 0.65}N surface (in heterostructure samples) is observed to decrease by {similar_to}0.60 eV with increase in barrier layer thickness from {similar_to}50 to {similar_to}440 Aa. A simple model considering the presence of a uniform density of charged acceptors in the Al{sub 0.35}Ga{sub 0.65}N layer is proposed to explain the observed decreasing trend in work function. {copyright} 2001 American Institute of Physics.

  9. Proton Dynamics in N,N,N?,N?-Tetramethyl-Guanidinium Bis(perfluoroethylsulfonyl)imide Protic Ionic Liquid Probed by Quasielastic Neutron Scattering

    SciTech Connect

    Mamontov, Eugene; Luo, Huimin; Dai, Sheng

    2009-01-01

    Using quasielastic neutron scattering, we have investigated diffusion dynamics of protons in the protic ionic liquid, N,N,N ,N -tetramethyl-guanidinium bis(perfluoroethylsulfonyl)imide, a promising new compound for application as an electrolyte in proton-conducting fuel cells. A temperature range of 30 K to 360 K has been studied. The melting temperature of N,N,N ,N -tetramethyl-guanidinium bis(perfluoroethylsulfonyl)imide is about 290 K. We have found four distinct dynamic processes. First, the methyl group rotations exhibit broadly distributed dynamics which, on the nanosecond time scale, become visible above approximately 100 K. Second, there is a localized process with a characteristic confinement radius of about 1.6 , which likely involves protons of the NH2 groups. These two processes take place in both solid and liquid phases, even though the methyl group rotations in the liquid phase are likely too fast to be detected in our experiment. Above the melting temperature, there are two new diffusion processes contributing to the dynamics of the liquid phase. Both of them appear to be of translational character. However, only the slower process represents unrestricted translation diffusion. The faster process is better described as spatially restricted translational diffusion with a characteristic confinement radius of about 8 . It is likely that the long-range proton transfer in N,N,N ,N -tetramethyl-guanidinium bis(perfluoroethylsulfonyl)imide is associated with the unrestricted translational diffusion process, which is characterized by a diffusion coefficient varying from 0.4*10^-10 to 1.4*10^-10 m2/s in the temperature range of 320 to 360 K.

  10. Absolute cross sections of electron attachment to molecular clusters. Part II: Formation of (H2O) N - , (N2O) N - , and (N2) N -

    NASA Astrophysics Data System (ADS)

    Vostrikov, A. A.; Dubov, D. Yu.

    2006-12-01

    Absolute cross sections σ-( E, N) of electron attachment to clusters (H2O) N , (N2O) N , and (N2) N for varying electron energy E and cluster size N are measured by using crossed electron and cluster beams in a vacuum. Continua of σ-( E) are found that correlate well with the functions of electron impact excitation of molecules’ internal degrees of freedom. The electron is attached through its solvation in a cluster. In the formation of (H2O){/N -}, (N2O){/N -}, and (N2){/N -}, the curves σ-( N) have a well-defined threshold because of a rise in the electron thermalization and solvation probability with N. For (H2O)900, (N2O)350, and (N2)260 clusters at E = 0.2 eV, the energy losses by the slow electron in the cluster are estimated as 3.0 × 107, 2.7 × 107, and 6.0 × 105 eV/m, respectively. It is found that the growth of σ- with N is the fastest for (H2O) N and (N2) N clusters at E → 0 as a result of polarization capture of the s-electron. Specifically, at E = 0.1 eV and N = 260, σ- = 3.0 × 10-13 cm2 for H2O clusters, 8.0 × 10-14 cm2 for N2O clusters, and 1.4 × 10-15 cm2 for N2 clusters; at E = 11 eV, σ- = 9.0 × 10-16 cm2 for (H2O)200 clusters, 2.4 × 10-14 cm2 for (N2O)350 clusters, and 5.0 × 10-17 cm2 for (N2)260 clusters; finally, at E = 30 eV, σ- = 3.6 × 10-17 cm2 for (N2O)10 clusters and 3.0 × 10-17 cm2 for (N2)125 clusters.

  11. Growth and Stress-induced Transformation of Zinc blende AlN Layers in Al-AlN-TiN Multilayers

    PubMed Central

    Li, Nan; Yadav, Satyesh K.; Wang, Jian; Liu, Xiang-Yang; Misra, Amit

    2015-01-01

    AlN nanolayers in sputter deposited {111}Al/AlN/TiN multilayers exhibit the metastable zinc-blende-structure (z-AlN). Based on density function theory calculations, the growth of the z-AlN is ascribed to the kinetically and energetically favored nitridation of the deposited aluminium layer. In situ nanoindentation of the as-deposited {111}Al/AlN/TiN multilayers in a high-resolution transmission electron microscope revealed the z-AlN to wurzite AlN phase transformation through collective glide of Shockley partial dislocations on every two {111} planes of the z-AlN. PMID:26681109

  12. Growth and stress-induced transformation of zinc blende AlN layers in Al-AlN-TiN multilayers

    DOE PAGES

    Li, Nan; Yadav, Satyesh K.; Wang, Jian; ...

    2015-12-18

    We report that AlN nanolayers in sputter deposited {111}Al/AlN/TiN multilayers exhibit the metastable zinc-blende-structure (z-AlN). Based on density function theory calculations, the growth of the z-AlN is ascribed to the kinetically and energetically favored nitridation of the deposited aluminium layer. In situ nanoindentation of the as-deposited {111}Al/AlN/TiN multilayers in a high-resolution transmission electron microscope revealed the z-AlN to wurzite AlN phase transformation through collective glide of Shockley partial dislocations on every two {111} planes of the z-AlN.

  13. Stranski-Krastanow growth of (1122)-oriented GaN/AlN quantum dots

    SciTech Connect

    Lahourcade, L.; Monroy, E.; Kehagias, T.; Dimitrakopulos, G. P.; Komninou, P.

    2009-03-16

    Semipolar GaN(1122) deposited on AlN(1122) by plasma-assisted molecular-beam epitaxy can follow the Frank-Van der Merwe or the Stranski-Krastanow growth mode as a function of the Ga/N ratio. N-rich grown GaN relaxes elastically at a critical thickness but the resulting GaN islands present multiple crystallographic orientations. In contrast, after deposition of a few two-dimensional GaN monolayers under Ga-rich conditions, a growth interruption in vacuum induces (1122)-oriented islanding. Applying this latter procedure, we have synthesized GaN/AlN quantum dot superlattices with reduced internal electric field.

  14. Parafoveal load of word N+1 modulates preprocessing effectiveness of word N+2 in Chinese reading.

    PubMed

    Yan, Ming; Kliegl, Reinhold; Shu, Hua; Pan, Jinger; Zhou, Xiaolin

    2010-12-01

    Preview benefits (PBs) from two words to the right of the fixated one (i.e., word N + 2) and associated parafoveal-on-foveal effects are critical for proposals of distributed lexical processing during reading. This experiment examined parafoveal processing during reading of Chinese sentences, using a boundary manipulation of N + 2-word preview with low- and high-frequency words N + 1. The main findings were (a) an identity PB for word N + 2 that was (b) primarily observed when word N + 1 was of high frequency (i.e., an interaction between frequency of word N + 1 and PB for word N + 2), and (c) a parafoveal-on-foveal frequency effect of word N + 1 for fixation durations on word N. We discuss implications for theories of serial attention shifts and parallel distributed processing of words during reading.

  15. AlN/GaN Metal Insulator Semiconductor Field Effect Transistor on Sapphire Substrate

    NASA Astrophysics Data System (ADS)

    Seo, Sanghyun; Ghose, Kaustav; Zhao, Guang Yuan; Pavlidis, Dimitris

    AlN/GaN Metal Insulator Semiconductor Field Effect Transistors (MISFETs) were designed, simulated and fabricated. DC, S-parameter and power measurements were also performed. Drift-diffusion simulations using DESSIS compared AlN/GaN MISFETs and Al32Ga68N/GaN Heterostructure FETs (HFETs) with the same geometries. The simulation results show the advantages of AlN/GaN MISFETs in terms of higher saturation current, lower gate leakage and higher transconductance than AlGaN/GaN HFETs. First results from fabricated AlN/GaN devices with 1μm gate length and 200μm gate width showed a maximum drain current density of ˜380mA/mm and a peak extrinsic transconductance of 85mS/mm. S-parameter measurements showed that currentgain cutoff frequency (fT) and maximum oscillation frequency (fmax) were 5.85GHz and 10.57GHz, respectively. Power characteristics were measured at 2GHz and showed output power density of 850mW/mm with 23.8% PAE at VDS=15V. To the authors knowledge this is the first report of a systematic study of AlN/GaN MISFETs addressing their physical modeling and experimental high-frequency characteristics including the power performance.

  16. Recombination of N4(+) ions with electrons

    NASA Technical Reports Server (NTRS)

    Cao, Y. S.; Johnsen, R.

    1991-01-01

    Using a modified high-pressure-afterglow/mass spectrometer apparatus similar to that described by Lee and Johnsen (1989), spectroscopic observations of afterglow helium plasmas, with N2 as a minor additive, were carried out in order to verify the mechanism suggested by Bates (1991) for dissociative recombination of electrons with N4(+) ions. It was found that dissociative recombination of electrons with N4(+) ions results in the formation of N2 molecules in the C 3Pi(u) (v = 0,1) state, with the recombination rate coefficient of (2.6 +/- 0.3) x 10 exp -6 cu cm/sec at 300 K.

  17. [Cu(N^N)(P^P)]+ complexes with 2,2':6',2''-terpyridine ligands as the N^N domain.

    PubMed

    Murray, Niamh S; Keller, Sarah; Constable, Edwin C; Housecroft, Catherine E; Neuburger, Markus; Prescimone, Alessandro

    2015-04-28

    The first examples of [Cu(N^N)(POP)](+) complexes (POP = bis(2-(diphenylphosphino)phenyl)ether) in which the N^N domain is a 2,2':6',2''-terpyridine (tpy) ligand have been prepared and characterized; N^N = tpy, 5,5''-dimethyl-2,2':6',2''-terpyridine (1), 4′-(4-tolyl)-2,2′:6′,2′′-terpyridine (2), 4′-(4-npropoxyphenyl)-2,2′:6′,2′′-terpyridine (3) and 4′-(4-nbutoxyphenyl)-2,2′:6′,2′′-terpyridine (4). In solution, the tpy domain in each [Cu(N^N)(POP)][PF6] complex is C2-symmetric, consistent with either tridentate coordination or a low energy dynamic process involving bidentate ligands; for [Cu(2)(POP)][PF6] and [Cu(4)(POP)][PF6], the (1)H NMR spectra showed negligible change between 295 and 210 K. The single crystal structures of [Cu(tpy)(POP)][PF6] and [Cu(4)(POP)][PF6] are presented. The asymmetric unit of [Cu(tpy)(POP)][PF6] contains two independent cations; in one the tpy ligand is tridentate and in the other, it is bidentate with the non-coordinated pyridine ring facing the Cu atom (Cu···N = 3.146(1) Å). In contrast, the solid-state structure of [Cu(4)(POP)][PF6] features a [Cu(4)(POP)](+) cation containing a bidentate tpy-domain with the non-coordinated pyridine ring oriented with the N-atom facing away from the Cu atom; this conformation may be associated with inter-cation NHC non-classical hydrogen bonds. The photophysical properties of [Cu(N^N)(POP)][PF6] with N^N = tpy or 1–4 are described. In the solid state at room temperature, the compounds are poorly emissive. In solution, the emission behaviour is consistent with ligand dissociation. This is supported by (1)H and (31)P NMR spectroscopic data which show POP and [Cu(POP)2](+) in solutions of aged samples; mass spectrometric data are consistent with the formation of [Cu(N^N)2](2+) in these samples.

  18. Syntheses, crystal structures, spectral study and DFT calculation of three new copper(II) complexes derived from pyridoxal hydrochloride, N,N-dimethylethylenediamine and N,N-diethylethylenediamine

    NASA Astrophysics Data System (ADS)

    Mandal, Senjuti; Naskar, Barnali; Modak, Ritwik; Sikdar, Yeasin; Chatterjee, Sudipta; Biswas, Sujan; Mondal, Tapan Kumar; Modak, Debadrita; Goswami, Sanchita

    2015-05-01

    Two pyridoxal containing Schiff bases obtained by condensation of pyridoxal hydrochloride with N,N-dimethylethylenediamine (HL1) and N,N-diethylethylenediamine (HL2) are used for the syntheses of three new copper (II) complexes [Cu(HL1)(H2O)Cl]Cl (1), [Cu(L1)Cl] (2) and [Cu(L2)Cl] (3). The single crystal X-ray structures of all the three copper(II) complexes are determined. Redox potentials for the mononuclear complexes are measured by cyclic voltammetry experiments. The DFT and TDDFT results have been used to interpret the experimental properties.

  19. catena-Poly[[[aqua(ethylenediamine-kappa2N,N')(nitrato-kappaO)copper(II)]-mu-4,4'-dithiodipyridine-kappa2N:N'] nitrate monohydrate].

    PubMed

    Seidel, Rüdiger W; Oppel, Iris M

    2009-07-01

    The title compound, {[Cu(NO(3))(C(2)H(4)N(2))(C(10)H(8)N(2)S(2))(H(2)O)]NO(3).H(2)O}(n), is composed of a one-dimensional linear coordination polymer involving cis-protected copper(II) ions and a 4,4'-dithiodipyridine bridging ligand. The polymeric chains run along the c-axis direction. N-H...O and O-H...O hydrogen bonds involving the coordinating amine groups, nitrate ions and water molecules, as well as cocrystallized noncoordinating nitrate ions and water molecules, generate a three-dimensional structure.

  20. N-(Quinoxalin-2-yl)-4-toluidine

    PubMed Central

    Wan Saffiee, Wan Ainna Mardhiah; Idris, Azila; Aiyub, Zaharah; Abdullah, Zanariah; Ng, Seik Weng

    2009-01-01

    The aromatic and the aromatic fused-rings in the title compound, C15H13N3, open the angle at the planar N atom to 130.07 (13) and 129.98 (13)° in the two independent mol­ecules in the asymmetric unit. The amino N atom of one mol­ecule forms a hydrogen bond to the 4-N atom of an adjacent quinoxalinyl ring, generating a supra­molecular chain. PMID:21581731

  1. Previrialization: Perturbative and N-Body Results

    NASA Astrophysics Data System (ADS)

    Lokas, E. L.; Juszkiewicz, R.; Bouchet, F. R.; Hivon, E.

    1996-08-01

    We present a series of N-body experiments which confirm the reality of the previrialization effect. We use also a weakly nonlinear perturbative approach to study the phenomenon. These two approaches agree when the rms density contrast, σ, is small; more surprisingly, they remain in agreement when σ ~ 1. When the slope of the initial power spectrum is n > -1, nonlinear tidal interactions slow down the growth of density fluctuations, and the magnitude of the suppression increases when n (i.e., the relative amount of small-scale power) is increased. For n < -1, we see an opposite effect: the fluctuations grow more rapidly than in linear theory. The transition occurs at n = -1 when the weakly nonlinear correction to σ is close to zero and the growth rate is close to linear. Our results resolve recent controversy between two N- body studies of previrialization. Peebles assumed n = 0 and found strong evidence in support of previrialization, while Evrard & Crone, who assumed n = -1, reached opposite conclusions. As we show here, the initial conditions with n = -1 are rather special because the nonlinear effects nearly cancel out for that particular spectrum. In addition to our calculations for scale-free initial spectra, we show results for a more realistic spectrum of Peacock & Dodds. Its slope near the scale usually adopted for normalization is close to -1, so σ is close to linear. Our results retroactively justify linear normalization at 8 h^-1^ Mpc while also demonstrating the danger and limitations of this practice.

  2. Aqueous complexation of trivalent lanthanide and actinide cations by N,N,N'{sub 2},N'-tetrakis(2-pyridylmethyl)ethylenediamine.

    SciTech Connect

    Beitz, J. V.; Ensor, D. D.; Jensen, M. P.; Morss, L. R.

    1999-06-16

    The aqueous complexation reactions of trivalent lanthanide and actinide cations with the hexadentate ligand N,N,N{prime},N{prime}-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN), have been characterized using potentiometric and spectroscopic techniques in 0.1 M NaClO{sub 4} At 25 C, the stability constant of Am(TPEN){sup 3+} is two orders of magnitude larger than that of Sm(TPEN){sup 3+}, reflecting the stronger interactions of the trivalent actinide cations with softer ligands as compared to lanthanide cations.

  3. First-principles phase diagram calculations for the rocksalt-structure quasibinary systems TiN-ZrN, TiN-HfN and ZrN-HfN

    NASA Astrophysics Data System (ADS)

    Liu, Z. T. Y.; Burton, B. P.; Khare, S. V.; Gall, D.

    2017-01-01

    We have studied the phase equilibria of three ceramic quasibinary systems Ti1-x Zr x N, Ti1-x Hf x N and Zr1-x Hf x N (0  ⩽  x  ⩽  1) with density functional theory, cluster expansion and Monte Carlo simulations. We predict consolute temperatures (T C), at which miscibility gaps close, for Ti1-x Zr x N to be 1400 K, for Ti1-x Hf x N to be 700 K, and below 200 K for Zr1-x Hf x N. The asymmetry of the formation energy ΔE f(x) is greater for Ti1-x Hf x N than Ti1-x Zr x N, with less solubility on the smaller cation TiN-side, and similar asymmetries were predicted for the corresponding phase diagrams. We also analyzed different energetic contributions: ΔE f of the random solid solutions were decomposed into a volume change term, Δ {{E}\\text{vc}} , and a chemical exchange and relaxation term, Δ {{E}\\text{xc\\text{-rlx}}} . These two energies partially cancel one another. We conclude that Δ {{E}\\text{vc}} influences the magnitude of T C and Δ {{E}\\text{xc\\text{-rlx}}} influences the asymmetry of ΔE f(x) and phase boundaries. We also conclude that the absence of experimentally observed phase separation in Ti1-x Zr x N and Ti1-x Hf x N is due to slow kinetics at low temperatures. In addition, elastic constants and mechanical properties of the random solid solutions were studied with the special quasirandom solution approach. Monotonic trends, in the composition dependence, of shear-related mechanical properties, such as Vickers hardness between 18 to 23 GPa, were predicted. Trends for Ti1-x Zr x N and Ti1-x Hf x N exhibit down-bowing (convexity). It shows that mixing nitrides of same group transition metals does not lead to hardness increase from an electronic origin, but through solution hardening mechanism. The mixed thin films show consistency and stability with little phase separation, making them desirable coating choices.

  4. First-principles phase diagram calculations for the rocksalt-structure quasibinary systems TiN-ZrN, TiN-HfN and ZrN-HfN.

    PubMed

    Liu, Z T Y; Burton, B P; Khare, S V; Gall, D

    2017-01-25

    We have studied the phase equilibria of three ceramic quasibinary systems Ti1-x Zr x N, Ti1-x Hf x N and Zr1-x Hf x N (0  ⩽  x  ⩽  1) with density functional theory, cluster expansion and Monte Carlo simulations. We predict consolute temperatures (T C), at which miscibility gaps close, for Ti1-x Zr x N to be 1400 K, for Ti1-x Hf x N to be 700 K, and below 200 K for Zr1-x Hf x N. The asymmetry of the formation energy ΔE f(x) is greater for Ti1-x Hf x N than Ti1-x Zr x N, with less solubility on the smaller cation TiN-side, and similar asymmetries were predicted for the corresponding phase diagrams. We also analyzed different energetic contributions: ΔE f of the random solid solutions were decomposed into a volume change term, [Formula: see text], and a chemical exchange and relaxation term, [Formula: see text]. These two energies partially cancel one another. We conclude that [Formula: see text] influences the magnitude of T C and [Formula: see text] influences the asymmetry of ΔE f(x) and phase boundaries. We also conclude that the absence of experimentally observed phase separation in Ti1-x Zr x N and Ti1-x Hf x N is due to slow kinetics at low temperatures. In addition, elastic constants and mechanical properties of the random solid solutions were studied with the special quasirandom solution approach. Monotonic trends, in the composition dependence, of shear-related mechanical properties, such as Vickers hardness between 18 to 23 GPa, were predicted. Trends for Ti1-x Zr x N and Ti1-x Hf x N exhibit down-bowing (convexity). It shows that mixing nitrides of same group transition metals does not lead to hardness increase from an electronic origin, but through solution hardening mechanism. The mixed thin films show consistency and stability with little phase separation, making them desirable coating choices.

  5. N,N,N-trimethylchitosan modified with well defined multifunctional polymer modules used as pDNA delivery vector.

    PubMed

    Ren, Hongqi; Liu, Shuai; Yang, Jixiang; Zhang, Xian; Zhou, Hao; Chen, Jiatong; Guo, Tianying

    2016-02-10

    A novel non-viral gene carrier based on N,N,N-trimethylchitosan (TMC) has been fabricated. First, well-defined copolymer P(PEGMA-co-DMAEMA) was synthesized through reversible addition fragmentation chain transfer (RAFT) polymerization of poly(ethylene glycol) methyl ether methacrylate (PEGMA) and N,N-(2-dimethylamino)ethyl methacrylamide (DMAEMA). Then allyl group grafting N,N,N-trimethylchitosan (Allyl-TMC) was synthesized via the reaction between allyl bromide and hydroxyl of TMC. Finally, P(PEGMA-co-DMAEMA) and folate were ordinally grafted onto Allyl-TMC to obtain TMC-g-P(PEGMA-co-DMAEMA)-FA. In comparison with pristine chitosan, TMC-g-P(PEGMA-co-DMAEMA)-FA has achieved both better water solubility and stronger pDNA packaging ability, which can contribute to improving gene transfection. Gene delivery efficiency of a series of TMC based functional polymers with different chitosan molecular weights has been tested. The results show that 20k-TMC-g-P(PEGMA-co-DMAEMA)-FA/pDNA complex at the weight ratio of 20 achieve the highest transfection efficiency in 293 T cells. This work presents a new strategy to modify chitosan efficiently as gene carrier material.

  6. Demonstration of isotype GaN/AlN/GaN heterobarrier diodes by NH{sub 3}-molecular beam epitaxy

    SciTech Connect

    Fireman, Micha N.; Browne, David A.; Mazumder, Baishakhi; Speck, James S.; Mishra, Umesh K.

    2015-05-18

    The results of vertical transport through nitride heterobarrier structures grown by ammonia molecular beam epitaxy are presented. Structures are designed with binary layers to avoid the effects of random alloy fluctuations in ternary nitride barriers. The unintentional incorporation of Ga in the AlN growth is investigated by atom probe tomography and is shown to be strongly dependent on both the NH{sub 3} flowrate and substrate temperature growth parameters. Once nominally pure AlN layer growth conditions are achieved, structures consisting of unintentionally doped (UID) GaN spacer layers adjacent to a nominally pure AlN are grown between two layers of n+ GaN, from which isotype diodes are fabricated. Varying the design parameters of AlN layer thickness, UID spacer layer thickness, and threading dislocation density show marked effects on the vertical transport characteristics of these structures. The lack of significant temperature dependence, coupled with Fowler-Nordheim and/or Milliken-Lauritsen analysis, point to a prevalently tunneling field emission mechanism through the AlN barrier. Once flatband conditions in the UID layer are achieved, electrons leave the barrier with significant energy. This transport mechanism is of great interest for applications in hot electron structures.

  7. Continuous formation of N-chloro-N,N-dialkylamine solutions in well-mixed meso-scale flow reactors

    PubMed Central

    Jolley, Katherine E

    2015-01-01

    Summary The continuous flow synthesis of a range of organic solutions of N,N-dialkyl-N-chloramines is described using either a bespoke meso-scale tubular reactor with static mixers or a continuous stirred tank reactor. Both reactors promote the efficient mixing of a biphasic solution of N,N-dialkylamine in organic solvent, and aqueous sodium hypochlorite to achieve near quantitative conversions, in 72–100% in situ yields, and useful productivities of around 0.05 mol/h with residence times from 3 to 20 minutes. Initial calorimetric studies have been carried out to inform on reaction exotherms, rates and safe operation. Amines which partition mainly in the organic phase require longer reaction times, provided by the CSTR, to compensate for low mass transfer rates in the biphasic system. The green metrics of the reaction have been assessed and compared to existing procedures and have shown the continuous process is improved over previous procedures. The organic solutions of N,N-dialkyl-N-chloramines produced continuously will enable their use in tandem flow reactions with a range of nucleophilic substrates. PMID:26734089

  8. Normally-off p-GaN/AlGaN/GaN high electron mobility transistors using hydrogen plasma treatment

    NASA Astrophysics Data System (ADS)

    Hao, Ronghui; Fu, Kai; Yu, Guohao; Li, Weiyi; Yuan, Jie; Song, Liang; Zhang, Zhili; Sun, Shichuang; Li, Xiajun; Cai, Yong; Zhang, Xinping; Zhang, Baoshun

    2016-10-01

    In this letter, we report a method by introducing hydrogen plasma treatment to realize normally-off p-GaN/AlGaN/GaN HEMT devices. Instead of using etching technology, hydrogen plasma was adopted to compensate holes in the p-GaN above the two dimensional electron gas (2DEG) channel to release electrons in the 2DEG channel and form high-resistivity area to reduce leakage current and increase gate control capability. The fabricated p-GaN/AlGaN/GaN HEMT exhibits normally-off operation with a threshold voltage of 1.75 V, a subthreshold swing of 90 mV/dec, a maximum transconductance of 73.1 mS/mm, an ON/OFF ratio of 1 × 107, a breakdown voltage of 393 V, and a maximum drain current density of 188 mA/mm at a gate bias of 6 V. The comparison of the two processes of hydrogen plasma treatment and p-GaN etching has also been made in this work.

  9. N2-fixing red alder indirectly accelerates ecosystem nitrogen cycling

    USGS Publications Warehouse

    Perakis, Steven S.; Matkins, Joselin J.; Hibbs, David E.

    2012-01-01

    Symbiotic N2-fixing tree species can accelerate ecosystem N dynamics through decomposition via direct pathways by producing readily decomposed leaf litter and increasing N supply to decomposers, as well as via indirect pathways by increasing tissue and detrital N in non-fixing vegetation. To evaluate the relative importance of these pathways, we compared three-year decomposition and N dynamics of N2-fixing red alder leaf litter (2.34 %N) to both low-N (0.68 %N) and high-N (1.21 %N) litter of non-fixing Douglas-fir, and decomposed each litter source in four forests dominated by either red alder or Douglas-fir. We also used experimental N fertilization of decomposition plots to assess elevated N availability as a potential mechanism of N2-fixer effects on litter mass loss and N dynamics. Direct effects of N2-fixing red alder on decomposition occurred primarily as faster N release from red alder than Douglas-fir litter, but direct increases in N supply to decomposers via fertilization did not stimulate decomposition of any litter. Fixed N indirectly influenced detrital dynamics by increasing Douglas-fir tissue and litter N concentrations, which accelerated litter N release without accelerating mass loss. By increasing soil N, tissue N, and the rate of N release from litter of non-fixers, we conclude that N2-fixing vegetation can indirectly foster plant-soil feedbacks that contribute to the persistence of elevated N availability in terrestrial ecosystems.

  10. Relative gas diffusivity as a controller of soil N2 and N2O fluxes

    NASA Astrophysics Data System (ADS)

    Clough, Tim; Balaine, Nimlesh; Beare, Mike; Thomas, Steve

    2015-04-01

    Animal grazing may induce soil compaction and has been shown to enhance emissions of the greenhouse gas nitrous oxide (N2O). The dominant substrate for N2O production is urea, supplied to the soil in ruminant urine. While studies have examined the effects of water-filled pore space on N2O emissions there has been less attention paid to the role of soil physical properties, such as relative gas diffusivity (Dp/Do), on N2O emissions and associated emissions of dinitrogen (N2). Three experiments were performed on soil cores maintained at a range of soil bulk densities (1.1 to 1.5 Mg/m3) and soil matric potentials (-10 to -0.2 kPa). These soil cores received urea at 700 kg N/ha to simulate a urine deposition event. Using the 15N tracer technique we measured N2 and N2O fluxes in order to investigate the role of soil Dp/Do as a controlling factor the magnitude of N2 and N2O fluxes and the reduction of N2O. As soil compaction and soil moisture contents increased soil Dp/Do declined. This in turn resulted in slower rates of nitrification. The mean cumulative fluxes of N2O, as a percentage of N applied, ranged from <1 to 16% after 35 days. Cumulative N2 fluxes as a percentage of N applied, ranged from <1 to 60% after 35 days. Soil compaction and soil matric potential interacted to influence Dp/Do which in turn was seen to be a strong determinant of the magnitude of both N2O and N2 fluxes. As Dp/Do values decreased a critical value was reached where N2O fluxes rapidly switched from being at a maximum to a minimum while at the same time N2 production intensified. This was also reflected in the N2:N2O ratios, based on cumulative fluxes, which ranged from <1 to 25. When compared with water-filled pore space the Dp/Do variable proved to be a better predictor of the switch from N2O production to N2 production.

  11. Inhibition of N-acetylneuraminate lyase by N-acetyl-4-oxo-D-neuraminic acid.

    PubMed

    Gross, H J; Brossmer, R

    1988-05-09

    We show that the 4-oxo analogue of N-acetyl-D-neuraminic acid strongly inhibits N-acetylneuraminate lyase (NeuAc aldolase, EC 4.1.3.3) from Clostridum perfringens (Ki = 0.025 mM) and Escherichia coli (Ki = 0.15 mM). In each case the inhibition was competitive. N-Acetyl-D-neuraminic acid; N-Acetylneuraminate lyase; N-Acetyl-D-neuraminic acid analog; 5-Acetamido-3,5-dideoxy-beta-D-manno-non-2,4-diulosonic acid; 2-Deoxy-2,3-didehydro-N-acetyl-4-oxo-neuraminic acid; Competitive inhibitor.

  12. Formation of N-Nitrosoterbuthylazine and N-Nitrosoterbutryn in a Model System of Soil Water.

    PubMed

    Trevisan; Graviani; Del Re AA; Arnoldi; Bassoli; Cova; Rossignoli

    1998-01-19

    The s-triazines terbutryn and terbuthylazine are currently used in Italy for weed control. A possible reaction of these compounds in the environment is N-nitrosation. Experiments performed in 10 mM CaCl(2) as a model of soil water indicated that N-nitrosation is favored only at low pH values and that the N-nitroso derivatives are fairly stable. In the presence of soil either parent compounds or N-nitroso derivatives are strongly adsorbed. These results seem to indicate that the possibility of formation of N-nitrosoterbuthylazine and N-nitrosoterbutryn in common agricultural soil is very remote.

  13. Indium Gallium Nitride/Gallium Nitride (InGaN/GaN) Nanorods Superlattice (SL)

    DTIC Science & Technology

    2006-03-10

    of high-brightness and high-efficiency LEDs using dislocation-free InGaN /GaN SL NRAs by hydride vapor phase epitaxy (HVPE). The benefits of the... InGaN /GaN SL NRA LEDs are examined in this work, and their characteristics are compared to those of conventional broad area(BA) LEDs . The NRs SL were...demonstrates realization of high-brightness and high-efficiency LEDs using dislocation-free InGaN /GaN SL Nano rods arrays (NRAs) by hydride vapor

  14. The transformations and fates of deposited N in an N saturated subtropical forested catchment, SW China

    NASA Astrophysics Data System (ADS)

    Zhu, Jing; Mulder, Jan; Dörsch, Peter

    2015-04-01

    Subtropical forests in south China are receiving long-term elevated nitrogen (N) deposition. Previous field observations in the N-saturated forested headwater catchment at Tieshanping (TSP), Chongqing, SW China, found apparent fast NH4+ disappearance in the top soil on the hillslope, but lab incubation for nitrification potentials did not support such disappearance. Meanwhile, large unaccounted N sinks were suggested by fast NO3- disappearance along the flow path in the groundwater discharge zone (GDZ), possibly due to denitrification and subsequent N2 emission. In this study, we investigated the fates of deposited N (mainly in the forms of NH4+ and NO3-) and the nature of the N transformations using isotopic tracer approach. 15N-labeled NH4+ or NO3- (99 atom% 15N) were amended to repacked surface soil columns from the hillslope and GDZ of TSP. The changes of the N forms of NH4+, NO3-, dissolved organic N, microbial biomass N and bulk N in soil were traced in a period of 15 days, representing transient (0.5 hr, 6 hr and 1 day) and mid-term (5 days and 15 days) N transformations. The soil moistures were kept at the typical field conditions (55% and 95% WFPS for hillslope soil and GDZ soil, respectively). Opposite to the field observations, the amount of added NH4+ decreased gradually on hillslope. 85% and 30% of the added 15N-NH4+ kept in the form of NH4+ after 1 day and 15 days. 15N-NO3- was produced gradually on hillslope, up to 26% of added 15N-NH4+ after 15 days incubation. About half of the added 15N-NH4+ was incorporated to organic N. The added 15N-NO3- showed a similar picture, with 55% left in the soil of hillslope after the whole incubation. Interestingly, although soil in GDZ had much higher WFPS, the nitrification rate of it was much higher than that on hillslope. Apparently the added 15N-NH4+ was incorporated immediately into organic matter in GDZ soil and being denitrified gradually along the time. The incorporation of the added 15N-NO3- into soil

  15. High-power UV InGaN/AlGaN double-heterostructure LEDs

    NASA Astrophysics Data System (ADS)

    Mukai, Takashi; Morita, Daisuke; Nakamura, Shuji

    1998-06-01

    Ultraviolet (UV) InGaN/AlGaN double-heterostructure (DH) light-emitting diodes (LEDs) with an external quantum efficiency of 7.5%, an output power of 5 mW and an emission wavelength of 371 nm were developed. High-power UV LEDs are obtained using an InGaN active layer with a thickness of 400 Å instead of a GaN active layer. The localized energy states caused by In composition fluctuation in the InGaN active layer are related to the high efficiency of the InGaN-based LEDs.

  16. Homoepitaxial growth of catalyst-free GaN wires on N-polar substrates

    NASA Astrophysics Data System (ADS)

    Chen, X. J.; Perillat-Merceroz, G.; Sam-Giao, D.; Durand, C.; Eymery, J.

    2010-10-01

    The shape of c-oriented GaN nanostructures is found to be directly related to the crystal polarity. As evidenced by convergent beam electron diffraction applied to GaN nanostructures grown by metal-organic vapor phase epitaxy on c-sapphire substrates: wires grown on nitridated sapphire have the N-polarity ([0001¯]) whereas pyramidal crystals have Ga-polarity ([0001]). In the case of homoepitaxy, the GaN wires can be directly selected using N-polar GaN freestanding substrates and exhibit good optical properties. A schematic representation of the kinetic Wulff's plot points out the effect of surface polarity.

  17. Ab initio modeling of zincblende AlN layer in Al-AlN-TiN multilayers

    DOE PAGES

    Yadav, S. K.; Wang, J.; Liu, X. -Y.

    2016-06-13

    An unusual growth mechanism of metastable zincblende AlN thin film by diffusion of nitrogen atoms into Al lattice is established. Using first-principles density functional theory, we studied the possibility of thermodynamic stability of AlN as a zincblende phase due to epitaxial strains and interface effect, which fails to explain the formation of zincblende AlN. We then compared the formation energetics of rocksalt and zincblende AlN in fcc Al through direct diffusion of nitrogen atoms to Al octahedral and tetrahedral interstitials. Furthermore, the formation of a zincblende AlN thin film is determined to be a kinetically driven process, not a thermodynamicallymore » driven process.« less

  18. Experimental and theoretical studies of the structural and electronic properties of vanadium-benzene sandwich clusters and their anions: V(n)Bz(n)(0/-) (n = 1-5) and V(n)Bz(n-1)(0/-) (n = 2-5).

    PubMed

    Masubuchi, Tsugunosuke; Iwasa, Takeshi; Nakajima, Atsushi

    2014-12-07

    One end open V(n)Bz(n)(-) (n = 1-5; Bz = benzene) and both ends open V(n)Bz(n-1)(-) (n = 2-5) vanadium-benzene cluster anions were studied using anion photoelectron spectroscopy and density functional calculations. The smaller (n ≤ 3) V(n)Bz(n) and V(n)Bz(n-1) clusters and corresponding anions were found to have structural isomers, whereas full-sandwiched V(n)Bz(n+1) clusters preferred to form multiple-decker sandwich structures. Several isomeric V2Bz2 structures were identified theoretically and the anion photoelectron spectra of V2Bz2(0/-) were explained well by the coexistence of two isomeric structures: (1) a V2-core structure sandwiched between benzene molecules and (2) an alternating sandwich structure with the spin state strongly dependent on the structure. The adiabatic electron affinity of both V(n)Bz(n) and V(n)Bz(n-1) was found to increase with the cluster size at larger sizes (n = 4 or 5) and approaches to that of V(n)Bz(n+1). The evolution of the structural and electronic properties of V(n)Bz(m) and V(n)Bz(m)(-) (m = n and n - 1) with size is discussed in comparison with V(n)Bz(n+1) and V(n)Bz(n+1)(-).

  19. Crystal structure of {(S)-1-phenyl-N,N-bis-[(pyridin-2-yl)meth-yl]ethanamine-κ(3)N,N',N''}bis-(thio-cyanato-κN)zinc from synchrotron data.

    PubMed

    Lee, Dong Won; Shin, Jong Won

    2017-01-01

    The title Zn(II) complex, [Zn(NCS)2(C20H21N3)], has been characterized by synchrotron single-crystal diffraction and FT-IR spectroscopy. The central Zn(II) ion has a distorted square-pyramidal coordination geometry, with three N atoms of the chiral (S) 1-phenyl-N,N-bis-[(pyridin-2-yl)meth-yl]ethanamine (S-ppme) ligand and one N atom of a thio-cyanate anion in the equatorial plane, and one N atom of another thio-cyanate anion at the apical position. The average Zn-N S-ppme and Zn-NNCS bond lengths are 2.183 (2) and 1.986 (2) Å, respectively. In the crystal, inter-molecular C-H⋯S hydrogen bonds and a face-to-face π-π inter-action [centroid-centroid distance = 3.482 (1) Å] link the mol-ecules and give rise to a supra-molecular sheet structure parallel to the ac plane.

  20. Isotopic investigations of dissolved organic N in soils identifies N mineralization as a major sink process

    NASA Astrophysics Data System (ADS)

    Wanek, Wolfgang; Prommer, Judith; Hofhansl, Florian

    2016-04-01

    Dissolved organic nitrogen (DON) is a major component of transfer processes in the global nitrogen (N) cycle, contributing to atmospheric N deposition, terrestrial N losses and aquatic N inputs. In terrestrial ecosystems several sources and sinks contribute to belowground DON pools but yet are hard to quantify. In soils, DON is released by desorption of soil organic N and by microbial lysis. Major losses from the DON pool occur via sorption, hydrological losses and by soil N mineralization. Sorption/desorption, lysis and hydrological losses are expected to exhibit no 15N fractionation therefore allowing to trace different DON sources. Soil N mineralization of DON has been commonly assumed to have no or only a small isotope effect of between 0-4‰, however isotope fractionation by N mineralization has rarely been measured and might be larger than anticipated. Depending on the degree of 15N fractionation by soil N mineralization, we would expect DON to become 15N-enriched relative to bulk soil N, and dissolved inorganic N (DIN; ammonium and nitrate) to become 15N-depleted relative to both, bulk soil N and DON. Isotopic analyses of soil organic N, DON and DIN might therefore provide insights into the relative contributions of different sources and sink processes. This study therefore aimed at a better understanding of the isotopic signatures of DON and its controls in soils. We investigated the concentration and isotopic composition of bulk soil N, DON and DIN in a wide range of sites, covering arable, grassland and forest ecosystems in Austria across an altitudinal transect. Isotopic composition of ammonium, nitrate and DON were measured in soil extracts after chemical conversion to N2O by purge-and-trap isotope ratio mass spectrometry. We found that delta15N values of DON ranged between -0.4 and 7.6‰, closely tracking the delta15N values of bulk soils. However, DON was 15N-enriched relative to bulk soil N by 1.5±1.3‰ (1 SD), and inorganic N was 15N