256 research outputs found

    Changes in psychological state in character disordered and neurotic patients

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    The Cationic Copolymerization of B-Pinene and Styrene

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    The Catatonic polymerization process is least well known of the polymerization mechanisms. Copolymerization by cationic initiation is not well understood. Charles Snyder began investigating the copolymerization of B-pinene and styrene in the fall of 1971, and found some intersting things. He reported, however, that the project was incomplete. This project was based on the work that Snyde began. The products he made, in addition to several others, were completely analyzed in an effort to obtain information about the cationic polymerization process. DSC, GPC, and solvent studies, along with VPO, were the methods of analysis

    Charge Transfer to Solvent Dynamics at the Ambient Water/Air Interface

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    Electron-transfer reactions at ambient aqueous interfaces represent one of the most fundamental and ubiquitous chemical reactions. Here the dynamics of the charge transfer to solvent (CTTS) reaction from iodide was probed at the ambient water/air interface by phase-sensitive transient second-harmonic generation. Using the three allowed polarization combinations, distinctive dynamics assigned to the CTTS state evolution and to the subsequent solvating electron-iodine contact pair have been resolved. The CTTS state is asymmetrically solvated in the plane of the surface, while the subsequent electron solvation dynamics are very similar to those observed in the bulk, although slightly faster. Between 3 and 30 ps, a small phase shift distinguishes an electron bound in a contact pair with iodine and a free hydrated electron at the water/air interface. Our results suggest that the hydrated electron is fully solvated in a region of reduced water density at the interface

    Ground Station Tracking System

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    One of the Eclipse Ballooning Project’s main goals was to stream live video of the eclipse to the internet. To accomplish this task a tracking antenna was built to follow the balloon payload. As an added challenge, the task had to be completed on a budget. The “ground station” is the center for communication between the payload and user. This system utilizes GPS position reports from the payload via the iridium network to determine the balloons position. The computer algorithm takes in additional GPS and IMU data from the ground station to determine a relative heading to orientate the antenna to point at the balloon payload. The heading and pitch are controlled with independent servos. These subsystems all jointly interact to keep the antenna pointed at the balloon to within a few degrees or the communication would be lost

    Band-dependent quasiparticle dynamics in the hole-doped Ba-122 iron pnictides

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    We report on band-dependent quasiparticle dynamics in the hole-doped Ba-122 pnictides measured by ultrafast pump-probe spectroscopy. In the superconducting state of the optimal and over hole-doped samples, we observe two distinct relaxation processes: a fast component whose decay rate increases linearly with excitation density and a slow component whose relaxation is independent of excitation strength. We argue that these two components reflect the recombination of quasiparticles in the two hole bands through intraband and interband processes. We also find that the thermal recombination rate of quasiparticles increases quadratically with temperature in all samples. The temperature and excitation density dependence of the decays indicates fully gapped hole bands and nodal or very anisotropic electron bands.United States. Department of Energy (Grant No. DE-FG02-08ER46521)National Science Foundation (U.S.). Materials Research Science and Engineering Centers (Program) (award number DMR - 0819762

    Professional Decisions and Ethical Values in Medical and Law Students

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    The purpose of this project is to evaluate and compare the values used by medical and law students when dealing with ethical dilemmas in the professional practice of law and medicine. It is assumed that conflict between doctors and lawyers often arises out of the different values that members of each profession apply to similar dilemmas

    Nonequilibrium Quasiparticle Relaxation Dynamics in Single Crystals of Hole and Electron doped BaFe2_2As2_2

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    We report on the nonequilibrium quasiparticle dynamics in BaFe2_2As2_2 on both the hole doped (Ba1x_{1-x}Kx_xFe2_2As2_2) and electron doped (BaFe2y_{2-y}Coy_yAs2_2) sides of the phase diagram using ultrafast pump-probe spectroscopy. Below TcT_c, measurements conducted at low photoinjected quasiparticle densities in the optimally and overdoped Ba1x_{1-x}Kx_xFe2_2As2_2 samples reveal two distinct relaxation processes: a fast component whose decay rate increases linearly with excitation density and a slow component with an excitation density independent decay rate. We argue that these two processes reflect the recombination of quasiparticles in the two hole bands through intraband and interband processes. We also find that the thermal recombination rate of quasiparticles increases quadratically with temperature in these samples. The temperature and excitation density dependence of the decays indicates fully gapped hole bands and nodal or very anisotropic electron bands. At higher excitation densities and lower hole dopings, the dependence of the dynamics on quasiparticle density disappears as the data are more readily understood in terms of a model which accounts for the quasiequilibrium temperature attained by the sample. In the BaFe2y_{2-y}Coy_yAs2_2 samples, dependence of the recombination rate on quasiparticle density at low dopings (i.e., y=0.12y=0.12) is suppressed upon submergence of the inner hole band and quasiparticle relaxation occurs in a slow, density independent manner.Comment: Accepted to Phys. Rev.

    Conservation of the structural and functional architecture of encapsulated ferritins in bacteria and archaea

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    Ferritins are a large family of intracellular proteins that protect the cell from oxidative stress by catalytically converting Fe(II) into less toxic Fe(III) and storing iron minerals within their core. Encapsulated ferritins (EncFtn) are a sub-family of ferritin-like proteins, which are widely distributed in all bacterial and archaeal phyla. The recently characterized Rhodospirillum rubrum EncFtn displays an unusual structure when compared with classical ferritins, with an open decameric structure that is enzymatically active, but unable to store iron. This EncFtn must be associated with an encapsulin nanocage in order to act as an iron store. Given the wide distribution of the EncFtn family in organisms with diverse environmental niches, a question arises as to whether this unusual structure is conserved across the family. Here, we characterize EncFtn proteins from the halophile Haliangium ochraceum and the thermophile Pyrococcus furiosus, which show the conserved annular pentamer of dimers topology. Key structural differences are apparent between the homologues, particularly in the centre of the ring and the secondary metal-binding site, which is not conserved across the homologues. Solution and native mass spectrometry analyses highlight that the stability of the protein quaternary structure differs between EncFtn proteins from different species. The ferroxidase activity of EncFtn proteins was confirmed, and we show that while the quaternary structure around the ferroxidase centre is distinct from classical ferritins, the ferroxidase activity is still inhibited by Zn(II). Our results highlight the common structural organization and activity of EncFtn proteins, despite diverse host environments and contexts within encapsulins
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