scholarly journals MODELING FLUID FLOWS IN DISTENSIBLE TUBES FOR APPLICATIONS IN HEMODYNAMICS

2013 ◽  
Vol 24 (05) ◽  
pp. 1350030 ◽  
Author(s):  
X. DESCOVICH ◽  
G. PONTRELLI ◽  
S. MELCHIONNA ◽  
S. SUCCI ◽  
S. WASSERTHEURER

We present a lattice Boltzmann (LB) model for the simulation of hemodynamic flows in the presence of compliant walls. The new scheme is based on the use of a continuous bounce-back boundary condition, as combined with a dynamic constitutive relation between the flow pressure at the wall and the resulting wall deformation. The method is demonstrated for the case of two-dimensional (axisymmetric) pulsatile flows, showing clear evidence of elastic wave propagation of the wall perturbation in response to the fluid pressure. The extension of the present two-dimensional axisymmetric formulation to more general three-dimensional geometries is currently under investigation.

1992 ◽  
Vol 238 ◽  
pp. 537-577 ◽  
Author(s):  
K. S. Yeo

This paper examines the linear stability of the Blasius boundary layer over compliant walls to three-dimensional (oblique) disturbance wave modes. The formulation of the eigenvalue problem is applicable to compliant walls possessing general material anisotropy. Isotropic-material walls and selected classes of anisotropic-material walls are studied. When the properties of the wall are identical with respect to all oblique wave directions, the stability eigenvalue problem for unstable three-dimensional wave modes may be reduced to an equivalent problem for two-dimensional modes. The results for isotropic-material walls show that three-dimensional Tollmien–Schlichting instability modes are more dominant than their two-dimensional counterparts when the walls are sufficiently compliant. The critical Reynolds number for Tollmien-Schlichting instability may be given by three-dimensional modes. Furthermore, for highly compliant walls, calculations based solely on two-dimensional modes are likely to underestimate the maximum disturbance growth factor needed for transition prediction and correlation. However, because the disturbance growth rates on highly compliant walls are much lower than those on a rigid wall, significant delay of transition may still be possible provided compliance-induced instabilities are properly suppressed. Walls featuring material anisotropy which have reduced stiffness to shear deformation in the transverse and oblique planes are also investigated. Such anisotropy is found to be effective in reducing the growth rates of the three-dimensional modes relative to those of the two-dimensional modes.


2007 ◽  
Vol 37 (9) ◽  
pp. 2331-2344 ◽  
Author(s):  
Sara Dubosq ◽  
Álvaro Viúdez

Abstract Frontal collisions of mesoscale baroclinic dipoles are numerically investigated using a three-dimensional, Boussinesq, and f-plane numerical model that explicitly conserves potential vorticity on isopycnals. The initial conditions, obtained using the potential vorticity initialization approach, consist of twin baroclinic dipoles, balanced (void of waves) and static and inertially stable, moving in opposite directions. The dipoles may collide in a close-to-axial way (cyclone–anticyclone collisions) or nonaxially (cyclone–cyclone or anticyclone–anticyclone collisions). The results show that the interacting vortices may bounce back and interchange partners, may merge reaching a tripole state, or may squeeze between the outer vortices. The formation of a stable tripole from two colliding dipoles is possible but is dependent on diffusion effects. It is found that the nonaxial dipole collisions can be characterized by the interchange between the domain-averaged potential and kinetic energy. Dipole collisions in two-dimensional flow display also a variety of vortex interactions, qualitatively similar to the three-dimensional cases.


Author(s):  
H.A. Cohen ◽  
T.W. Jeng ◽  
W. Chiu

This tutorial will discuss the methodology of low dose electron diffraction and imaging of crystalline biological objects, the problems of data interpretation for two-dimensional projected density maps of glucose embedded protein crystals, the factors to be considered in combining tilt data from three-dimensional crystals, and finally, the prospects of achieving a high resolution three-dimensional density map of a biological crystal. This methodology will be illustrated using two proteins under investigation in our laboratory, the T4 DNA helix destabilizing protein gp32*I and the crotoxin complex crystal.


Author(s):  
B. Ralph ◽  
A.R. Jones

In all fields of microscopy there is an increasing interest in the quantification of microstructure. This interest may stem from a desire to establish quality control parameters or may have a more fundamental requirement involving the derivation of parameters which partially or completely define the three dimensional nature of the microstructure. This latter categorey of study may arise from an interest in the evolution of microstructure or from a desire to generate detailed property/microstructure relationships. In the more fundamental studies some convolution of two-dimensional data into the third dimension (stereological analysis) will be necessary.In some cases the two-dimensional data may be acquired relatively easily without recourse to automatic data collection and further, it may prove possible to perform the data reduction and analysis relatively easily. In such cases the only recourse to machines may well be in establishing the statistical confidence of the resultant data. Such relatively straightforward studies tend to result from acquiring data on the whole assemblage of features making up the microstructure. In this field data mode, when parameters such as phase volume fraction, mean size etc. are sought, the main case for resorting to automation is in order to perform repetitive analyses since each analysis is relatively easily performed.


Author(s):  
Yu Liu

The image obtained in a transmission electron microscope is the two-dimensional projection of a three-dimensional (3D) object. The 3D reconstruction of the object can be calculated from a series of projections by back-projection, but this algorithm assumes that the image is linearly related to a line integral of the object function. However, there are two kinds of contrast in electron microscopy, scattering and phase contrast, of which only the latter is linear with the optical density (OD) in the micrograph. Therefore the OD can be used as a measure of the projection only for thin specimens where phase contrast dominates the image. For thick specimens, where scattering contrast predominates, an exponential absorption law holds, and a logarithm of OD must be used. However, for large thicknesses, the simple exponential law might break down due to multiple and inelastic scattering.


Author(s):  
D. E. Johnson

Increased specimen penetration; the principle advantage of high voltage microscopy, is accompanied by an increased need to utilize information on three dimensional specimen structure available in the form of two dimensional projections (i.e. micrographs). We are engaged in a program to develop methods which allow the maximum use of information contained in a through tilt series of micrographs to determine three dimensional speciman structure.In general, we are dealing with structures lacking in symmetry and with projections available from only a limited span of angles (±60°). For these reasons, we must make maximum use of any prior information available about the specimen. To do this in the most efficient manner, we have concentrated on iterative, real space methods rather than Fourier methods of reconstruction. The particular iterative algorithm we have developed is given in detail in ref. 3. A block diagram of the complete reconstruction system is shown in fig. 1.


Author(s):  
A.M. Jones ◽  
A. Max Fiskin

If the tilt of a specimen can be varied either by the strategy of observing identical particles orientated randomly or by use of a eucentric goniometer stage, three dimensional reconstruction procedures are available (l). If the specimens, such as small protein aggregates, lack periodicity, direct space methods compete favorably in ease of implementation with reconstruction by the Fourier (transform) space approach (2). Regardless of method, reconstruction is possible because useful specimen thicknesses are always much less than the depth of field in an electron microscope. Thus electron images record the amount of stain in columns of the object normal to the recording plates. For single particles, practical considerations dictate that the specimen be tilted precisely about a single axis. In so doing a reconstructed image is achieved serially from two-dimensional sections which in turn are generated by a series of back-to-front lines of projection data.


Author(s):  
Douglas L. Dorset ◽  
Andrew K. Massalski

Matrix porin, the ompF gene product of E. coli, has been the object of a electron crystallographic study of its pore geometry in an attempt to understand its function as a membrane molecular sieve. Three polymorphic forms have been found for two-dimensional crystals reconstituted in phospholipid, two hexagonal forms with different lipid content and an orthorhombic form coexisting with and similar to the hexagonal form found after lipid loss. In projection these have been shown to retain the same three-fold pore triplet geometry and analyses of three-dimensional data reveal that the small hexagonal and orthorhombic polymorphs have similar structure as well as unit cell spacings.


Author(s):  
Jeffry A. Reidler ◽  
John P. Robinson

We have prepared two-dimensional (2D) crystals of tetanus toxin using procedures developed by Uzgiris and Kornberg for the directed production of 2D crystals of monoclonal antibodies at an antigen-phospholipid monolayer interface. The tetanus toxin crystals were formed using a small mole fraction of the natural receptor, GT1, incorporated into phosphatidyl choline monolayers. The crystals formed at low concentration overnight. Two dimensional crystals of this type are particularly useful for structure determination using electron microscopy and computer image refinement. Three dimensional (3D) structural information can be derived from these crystals by computer reconstruction of photographs of toxin crystals taken at different tilt angles. Such 3D reconstructions may help elucidate the mechanism of entry of the enzymatic subunit of toxins into cells, particularly since these crystals form directly on a membrane interface at similar concentrations of ganglioside GT1 to the natural cellular receptors.


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