Remarks on Hawking radiation as tunneling from the BTZ black holes

Hawking radiation viewed as a semiclassical tunneling process from the event horizon of the (2 + 1)-dimensional rotating BTZ black hole is carefully reexamined by taking into account not only the energy conservation but also the conservation of angular momentum when the effect of the emitted particle's self-gravitation is incorporated. In contrast to previous analysis of this issue in the literature, our result obtained here fits well to the Kraus-Parikh-Wilczek's universal conclusion without any modification to the Bekenstein-Hawking area-entropy formulae of the BTZ black hole.Comment: 12pages, no figure, use JHEP3.cls. Version better than published one in JHE

Optical properties and radiative forcing of urban aerosols in Nanjing, China

AbstractContinuous measurements of atmospheric aerosols were made in Nanjing, a megacity in China, from 18 January to 18 April, 2011 (Phase 1) and from 22 April 2011 to 21 April 2012 (Phase 2). Aerosol characteristics, optical properties, and direct radiative forcing (DRF) were studied through interpretations of these measurements. We found that during Phase 1, mean PM2.5, black carbon (BC), and aerosol scattering coefficient (Bsp) in Nanjing were 76.1 ± 59.3 μg m−3, 4.1 ± 2.2 μg m−3, and 170.9 ± 105.8 M m−1, respectively. High pollution episodes occurred during Spring and Lantern Festivals when hourly PM2.5 concentrations reached 440 μg m−3, possibly due to significant discharge of fireworks. Temporal variations of PM2.5, BC, and Bsp were similar to each other. It is estimated that inorganic scattering aerosols account for about 49 ± 8.6% of total aerosols while BC only accounted for 6.6 ± 2.9%, and nitrate was larger than sulfate. In Phase 2, optical properties of aerosols show great seasonality. High relative humidity (RH) in summer (June, July, August) likely attributed to large optical depth (AOD) and small Angstrom exponent (AE) of aerosols. Due to dust storms, AE of total aerosols was the smallest in spring (March, April, May). Annual mean 550-nm AOD and 675/440-nm AE were 0.6 ± 0.3 and 1.25 ± 0.29 for total aerosols, 0.04 ± 0.02 and 1.44 ± 0.50 for absorbing aerosols, 0.48 ± 0.29 and 1.64 ± 0.29 for fine aerosols, respectively. Annual single scattering albedo of aerosols ranged from 0.90 to 0.92. Real time wavelength-dependent surface albedo from the Moderate Resolution Imaging Spectroradiometer (MODIS) was used to assess aerosol DRFs. Both total and absorbing aerosol DRFs had significant seasonal variations in Nanjing and they were the strongest in summer. Annual mean clear sky TOA DRF (including daytime and nighttime) of total and absorbing aerosols was about −6.9 and +4.5 W m−2, respectively. Aerosol DRFs were found to be sensitive to surface albedo. Over brighter surfaces, solar radiation was more absorbed by absorbing aerosols and less scattered by scattering aerosols

Fabrication and Properties of Composites of Poly(ethylene oxide) and Functionalized Carbon Nanotubes

Carbon nanotubes (CNTs) [1, 2] have dimensions similar to those of typical polymeric chains, with 1-50nm in diameter and 1-10μm in length. Experimental results on individual carbon nanotubes and nanotube bundles show that they have exceptional electrical and mechanical properties with an elastic modulus of ~1TPa and fracture strain of 5-10%. [3] The thermal conductivity of the nanotubes is expected to be higher than that of the carbon fibers because of their structural perfection. As a result there are considerable interests in utilization of CNTs as fillers for thermal management and structural reinforcement. Although there have been several published studies on polymer-CNT composites [4-9], realization of the expected enhancement in properties, especially mechanical properties, has by and large not been demonstrated. This is in part because of the difficulties in materials processing arising from insolubility of the pristine CNTs

A molecular dynamics simulation of polymer crystallization from oriented amorphous state

Molecular process of crystallization from an oriented amorphous state was reproduced by molecular dynamics simulation for a realistic polyethylene model. Initial oriented amorphous state was obtained by uniaxial drawing an isotropic glassy state at 100 K. By the temperature jump from 100 K to 330 K, there occurred the crystallization into the fiber structure, during the process of which we observed the developments of various order parameters. The real space image and its Fourier transform revealed that a hexagonally ordered domain was initially formed, and then highly ordered crystalline state with stacked lamellae developed after further adjustment of the relative heights of the chains along their axes.Comment: 4 pages, 3 figure