289 research outputs found

    Electron Paramagnetic Resonance Imaging of the Spatial Distribution of Free Radicals in PMR-15 Polyimide Resins

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    Prior studies have shown that free radicals generated by heating polyimides above 300 C are stable at room temperature and are involved in thermo-oxidative degradation in the presence of oxygen gas. Electron Paramagnetic Resonance Imaging (EPRI) is a technique to determine the spatial distribution of free radicals. X-band (9.5 GHz) EPR images of PMR-15 polyimide were obtained with a spatial resolution of about 0.18 mm along a 2 mm dimension of the sample. In a polyimide sample that was not thermocycled, the radical distribution was uniform along the 2 mm dimension of the sample. For a polyimide sample that was exposed to thermocycling in air for 300 one-hour cycles at 335 C, one-dimensional EPRI showed a higher concentration of free radicals in the surface layers than in the bulk sample. A spectral-spatial two-dimensional image showed that the EPR lineshape of the surface layer remained the same as that of the bulk. These EPRI results suggest that the thermo-oxidative degradation of PMR-15 resin involves free radicals present in the oxygen-rich surface layer

    Greybody Factors of Charged Dilaton Black Holes in 2 + 1 Dimensions

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    We have studied scalar perturbations of charged dilaton black holes in 2+1 dimensions. The black hole considered here is a solution to the low-energy string theory in 2+1 dimensions. The exact decay rates and the grey body factors for the massless minimally coupled scalar is computed for both the charged and the uncharged dilaton black holes. The charged and the uncharged black hole show similar behavior for grey body factors, reflection coefficients and decay rates.Comment: The equation for the potential and figure:1 are changed. The changes does not effect the result

    Spatiotemporal variations of air pollutants (O-3, NO2, SO2, CO, PM10, and VOCs) with land-use types

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    The spatiotemporal variations of surface air pollutants (O-3, NO2, SO2, CO, and PM10) with four land-use types, residence (R), commerce (C), industry (I) and greenbelt (G), have been investigated at 283 stations in South Korea during 2002-2013, using routinely observed data. The volatile organic compound (VOC) data at nine photochemical pollutant monitoring stations available since 2007 were utilized in order to examine their effect on the ozone chemistry. The land-use types, set by the Korean government, were generally consistent with the satellite-derived land covers and with the previous result showing anti-correlation between O-3 and NO2 in diverse urban areas. The relationship between the two pollutants in the Seoul Metropolitan Area (SMA) residence land-use areas was substantially different from that outside of the SMA, probably due to the local differences in vehicle emissions. The highest concentrations of air pollutants in the diurnal, weekly, and annual cycles were found in industry for SO2 and PMPM10, in commerce for NO2 and CO, and in greenbelt for O-3. The concentrations of air pollutants, except for O-3, were generally higher in big cities during weekdays, while O-3 showed its peak in suburban areas or small cities during weekends. The weekly cycle and trends of O-3 were significantly out of phase with those of NO2, particularly in the residential and commercial areas, suggesting that vehicle emission was a major source in those areas. The ratios of VOCs to NO2 for each of the land-use types were in the order of I (10.2) > C (8.7) > G (3.9) > R (3.6), suggesting that most areas in South Korea were likely to be VOC-limited for ozone chemistry. The pollutants (NO2, SO2, CO, and PMPM10 except for O-3 have decreased, most likely due to the effective government control. The total oxidant values (OX = O-3 + NO2) with the land-use types were analyzed for the local and regional (or background) contributions of O-3, respectively, and the order of OX (ppb) was C (57.4) > R (53.6) > I (50.7) > G (45.4), indicating the greenbelt observation was close to the backgroundopen

    Non-Newtonian Couette-Poiseuille flow of a dilute gas

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    The steady state of a dilute gas enclosed between two infinite parallel plates in relative motion and under the action of a uniform body force parallel to the plates is considered. The Bhatnagar-Gross-Krook model kinetic equation is analytically solved for this Couette-Poiseuille flow to first order in the force and for arbitrary values of the Knudsen number associated with the shear rate. This allows us to investigate the influence of the external force on the non-Newtonian properties of the Couette flow. Moreover, the Couette-Poiseuille flow is analyzed when the shear-rate Knudsen number and the scaled force are of the same order and terms up to second order are retained. In this way, the transition from the bimodal temperature profile characteristic of the pure force-driven Poiseuille flow to the parabolic profile characteristic of the pure Couette flow through several intermediate stages in the Couette-Poiseuille flow are described. A critical comparison with the Navier-Stokes solution of the problem is carried out.Comment: 24 pages, 5 figures; v2: discussion on boundary conditions added; 10 additional references. Published in a special issue of the journal "Kinetic and Related Models" dedicated to the memory of Carlo Cercignan

    Geometry of Polynomials and Root-Finding via Path-Lifting

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    Using the interplay between topological, combinatorial, and geometric properties of polynomials and analytic results (primarily the covering structure and distortion estimates), we analyze a path-lifting method for finding approximate zeros, similar to those studied by Smale, Shub, Kim, and others. Given any polynomial, this simple algorithm always converges to a root, except on a finite set of initial points lying on a circle of a given radius. Specifically, the algorithm we analyze consists of iterating zf(z)tkf(z0)f(z)z - \frac{f(z)-t_kf(z_0)}{f'(z)} where the tkt_k form a decreasing sequence of real numbers and z0z_0 is chosen on a circle containing all the roots. We show that the number of iterates required to locate an approximate zero of a polynomial ff depends only on logf(z0)/ρζ\log|f(z_0)/\rho_\zeta| (where ρζ\rho_\zeta is the radius of convergence of the branch of f1f^{-1} taking 00 to a root ζ\zeta) and the logarithm of the angle between f(z0)f(z_0) and certain critical values. Previous complexity results for related algorithms depend linearly on the reciprocals of these angles. Note that the complexity of the algorithm does not depend directly on the degree of ff, but only on the geometry of the critical values. Furthermore, for any polynomial ff with distinct roots, the average number of steps required over all starting points taken on a circle containing all the roots is bounded by a constant times the average of log(1/ρζ)\log(1/\rho_\zeta). The average of log(1/ρζ)\log(1/\rho_\zeta) over all polynomials ff with dd roots in the unit disk is O(d){\mathcal{O}}({d}). This algorithm readily generalizes to finding all roots of a polynomial (without deflation); doing so increases the complexity by a factor of at most dd.Comment: 44 pages, 12 figure

    Visualizing helicases unwinding DNA at the single molecule level

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    DNA helicases are motor proteins that catalyze the unwinding of double-stranded DNA into single-stranded DNA using the free energy from ATP hydrolysis. Single molecule approaches enable us to address detailed mechanistic questions about how such enzymes move processively along DNA. Here, an optical method has been developed to follow the unwinding of multiple DNA molecules simultaneously in real time. This was achieved by measuring the accumulation of fluorescent single-stranded DNA-binding protein on the single-stranded DNA product of the helicase, using total internal reflection fluorescence microscopy. By immobilizing either the DNA or helicase, localized increase in fluorescence provides information about the rate of unwinding and the processivity of individual enzymes. In addition, it reveals details of the unwinding process, such as pauses and bursts of activity. The generic and versatile nature of the assay makes it applicable to a variety of DNA helicases and DNA templates. The method is an important addition to the single-molecule toolbox available for studying DNA processing enzymes
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