scholarly journals Thermodynamics of (1+1) dilatonic black holes in global flat embedding scheme

2005 ◽  
Vol 623 (1-2) ◽  
pp. 135-140 ◽  
Author(s):  
Soon-Tae Hong
Keyword(s):  
Black Holes ◽  
Flat Embedding

scholarly journals Global embeddings and hydrodynamic properties of Kerr black hole

2016 ◽  
Vol 31 (35) ◽  
pp. 1650204
Author(s):  
Soon-Tae Hong
Keyword(s):  
Black Holes ◽  
Black Hole ◽  
Equatorial Plane ◽  
Kerr Black Hole ◽  
Kerr Spacetime ◽  
Stable Circular Orbit ◽  
Massive Particles ◽  
Flat Embedding ◽  
Bound Orbits ◽  
The Impact

In the presence of a rotating Kerr black hole, we investigate hydrodynamics of the massive particles and massless photons to construct relations among number density, pressure and internal energy density of the massive particles and photons around the rotating Kerr black hole and to study an accretion onto the black hole. On equatorial plane of the Kerr black hole, we investigate the bound orbits of the massive particles and photons around the black hole to produce their radial, azimuthal and precession frequencies. With these frequencies, we study the black holes GRO J1655-40 and 4U 1543-47 to explicitly obtain the radial, azimuthal and precession frequencies of the massive particles in the flow of perfect fluid. We next consider the massive particles in the stable circular orbit of radius of 1.0 ly around the supernovas SN 1979C, SN 1987A and SN 2213-1745 in the Kerr curved spacetime, and around the potential supermassive Schwarzschild black holes M87, NGC 3115, NGC 4594, NGC 3377, NGC 4258, M31, M32 and Galatic center, to estimate their radial and azimuthal frequencies, which are shown to be the same results as those in no precession motion. The photon unstable orbit is also discussed in terms of the impact parameter of the photon trajectory. Finally, on the equatorial plane of the Kerr black hole, we construct the global flat embedding structures possessing (9 + 3) dimensionalities outside and inside the event horizon of the rotating Kerr black hole. Moreover, on the plane, we investigate the warp products of the Kerr spacetime.

Ultramicrotomy as a Technique for Materials Specimen Preparation

1990 ◽  
Vol 48 (2) ◽  
pp. 428-429
Author(s):  
S.R. Glanvill
Keyword(s):  
Materials Science ◽  
Structural Information ◽  
Specimen Preparation ◽  
Preparation Technique ◽  
Cross Sectional ◽  
Surfaces And Interfaces ◽  
Beam Analysis ◽  
Flat Embedding ◽  
20 Nm ◽  
Sectional Analysis

This paper summarizes the application of ultramicrotomy as a specimen preparation technique for some of the Materials Science applications encountered over the past two years. Specimens 20 nm thick by hundreds of μm lateral dimension are readily prepared for electron beam analysis. Materials examined include metals, plastics, ceramics, superconductors, glassy carbons and semiconductors. We have obtain chemical and structural information from these materials using HRTEM, CBED, EDX and EELS analysis. This technique has enabled cross-sectional analysis of surfaces and interfaces of engineering materials and solid state electronic devices, as well as interdiffusion studies across adjacent layers.Samples are embedded in flat embedding moulds with Epon 812 epoxy resin / Methyl Nadic Anhydride mixture, using DY064 accelerator to promote the reaction. The embedded material is vacuum processed to remove trapped air bubbles, thereby improving the strength and sectioning qualities of the cured block. The resin mixture is cured at 60 °C for a period of 80 hr and left to equilibrate at room temperature.

Flat embeddment of monolayer cells, tissue sections, and other cellular materials attached onto glass substrate

1990 ◽  
Vol 48 (3) ◽  
pp. 766-767
Author(s):  
Jeffrey P. Chang ◽  
Jaang J. Wang
Keyword(s):  
Present Report ◽  
Cellular Materials ◽  
Cover Glass ◽  
Tissue Sections ◽  
Embedding Technique ◽  
Exfoliated Cells ◽  
Black Paper ◽  
Cell Concentrations ◽  
Flat Embedding

Flat embeddment of certain specimens for electron microscopy is necessary for three classes of biological materials: namely monolayer cells, tissue sections of paraffin or plastics, as well as cell concentrations, exfoliated cells, and cell smears. The present report concerns a flat-embedding technique which can be applied to all these three classes of materials and which is a modified and improved version of Chang's original methodology.Preparation of coverglasses and microslides. Chemically cleaned coverglasses, 11 × 22 mm or other sizes, are laid in rows on black paper. Ink-mark one coner for identifying the spray-side of the glass for growing cells. Lightly spray with Teflon monomer (Heddy/Contact Inductries, Paterson, NO 07524, U.S.A.) from a pressurized can. Bake the sprayed glasses at 500°F for 45 min on Cover-Glass Ceramic Racks (A. Thomas Co. Philadelphia), for Teflon to polymerize.Monolayer Cells. After sterilization, the Teflon-treated coverglasses, with cells attached, are treated or fixed in situ in Columbia staining dishes (A. Thomas Co., Philadelphia) for subsequent processing.

Involvement of nucleus in the maturation of dengue-2 virus in C6/36 cells

1990 ◽  
Vol 48 (3) ◽  
pp. 912-913
Author(s):  
Jaang J. Wang ◽  
Cheng C. Chen ◽  
Men F. Shaio ◽  
Chia T. Liu ◽  
Chung S. Lee ◽  
...  
Keyword(s):  
Culture Medium ◽  
Cytopathic Effect ◽  
Fetal Bovine Serum ◽  
Virus Particles ◽  
Electron Microscopies ◽  
Embedding Technique ◽  
Fetal Bovine ◽  
Flat Embedding ◽  
20 Nm ◽  
Labeling Method

The involvement of nucleus in the maturation processes of Dengue-2 virus in a mosquito cell line, C6/36 cells, has been identified by the electron microscopy and immunocytochemistry. The C6/36 cells were obtained from ATCC and maintained in MEM culture medium containing 10% fetal bovine serum at 28°C. The cell suspensions or cells grown on teflon-coated coverslips were infected with Dengue-2 virus (107/ml) for various time periods of 2 hours, 3, 6, 8, and 10 days. The cells were then fixed in buffered 1.5% glutaraldehyde, and washed in acetone before immunolabeled with monoclonal antibody. An indirect immunocytochemical labeling method of avidin-biotin complex (ABC) conjugated with peroxidase or gold particles (20 nm in diameter) and a flat embedding technique were used to localize the virus particles.At early stages of infections (before 3 days), there were no virion particles detected. After 6 days and on of infections, cytopathic effect (CPE) was observed and showed positive immuno-peroxidase reactions under the light and electron microscopies.

Black holes have ring of truth

Nature ◽  
2002 ◽  
Author(s):  
Philip Ball
Keyword(s):  
Black Holes
Sign in / Sign up

Export Citation Format

Share Document