scholarly journals Three-Dimensional Interaction of Viscous Fingering and Gravitational Segregation in Porous Media

Fluids ◽  
2019 ◽  
Vol 4 (3) ◽  
pp. 130 ◽  
Author(s):  
Tetsuya Suekane ◽  
Tomotaka Koe ◽  
Pablo Marin Barbancho

Viscous fingering is fluid dynamics instability induced on the displacement front when a less viscous fluid (LVF) displaces a more viscous fluid (MVF), thereby reducing the displacement efficiency. The displacement of a denser fluid by a less dense fluid produces a gravitational tongue. This gravitational segregation also reduces the displacement efficiency. In this study, the three-dimensional structure of the fingering pattern at the viscous fingering to gravitational segregation boundary was examined using X-ray microtomography on a packed bed of particles. At low gravity numbers, viscous fingering resembled that without gravity characterized by nonlinear interaction including tip-splitting, shielding, and coalescence. At intermediate gravity numbers, viscous fingering is associated with the gravitational tongue due to segregation. At high gravity numbers, a clear gravitational tongue penetrates from the inlet to the outlet. Consequently, the concentration near the injection point decreases and exhibits a flat profile in the flow direction. The displacement efficiency decreases with increasing gravity number, with the highest value achieved without gravity but depends on many factors, including the viscosity ratio and Péclet number.

1976 ◽  
Vol 98 (4) ◽  
pp. 635-643 ◽  
Author(s):  
Y. Furuya ◽  
M. Miyata ◽  
H. Fujita

The flow resistance in a plate roughened by equally spaced wires at right angles to the flow direction was investigated experimentally by measuring the turbulent boundary layer developing along it. Measurements of pressure distribution around a roughness element revealed that the pressure drag accounts for a large portion of the surface resistance and remaining skin frictional part is almost equal to that of a smooth plate. Measurements were also made for plates having three-dimensional roughness. These plates were roughened by short wires in a staggered manner. In this case, the boundary layer was found to have a three-dimensional structure due to accompanying secondary currents.


1988 ◽  
Vol 190 ◽  
pp. 1-37 ◽  
Author(s):  
E. Meiburg ◽  
J. C. Lasheras

The three-dimensional structure of a moderate-Reynolds-number (≈ 100) plane wake behind a flat plate subjected to periodic spanwise perturbations has been studied both experimentally and numerically. Comparisons between experimental interface visualizations and numerical calculations demonstrate that important features of the development of the three-dimensional evolution can be reproduced by numerical inviscid vortex dynamics.It is shown that the redistribution, reorientation and stretching of vorticity leads to the formation of counter-rotating pairs of streamwise vortices which superimpose onto the spanwise Kármán-like vortices. These streamwise vortices exhibit lambdashaped structures and are located in the braids connecting consecutive Kármán vortices of opposite sign.The interaction of the evolving streamwise structure with the spanwise Kármán vortices results in the formation of closed vortex loops. Depending on the orientation of the initial perturbation, the three-dimensional vorticity field of the wake acquires either a symmetric or a non-symmetric configuration. Under the effect of a periodic vertical perturbation, the wake develops a non-symmetric vorticity mode exhibiting a staggered array of closed vortex loops of alternating sign. In contrast, under the effect of a periodic horizontal perturbation, the wake acquires a symmetric vorticity mode with the closed vortex loops of alternating sign aligned in the flow direction.


Author(s):  
Mariya S. Deryabina ◽  
Sergey I. Martynov

In the Stokes approximation, the problem of viscous fluid flow through two-dimensional and three-dimensional periodic structures is solved. A system of thin plates of a finite width is considered as a two-dimensional structure, and a system of thin rods of finite length is considered as a three-dimensional structure. Plates and rods are periodically located in space with certain translation steps along mutually perpendicular axes. On the basis of the procedure developed earlier, the authors constructed an approximate solution of the equations for fluid flow with an arbitrary orientation of structures relative to a given vector of pressure gradient. The solution is sought in a finite region (cells) around inclusions in the class of piecewise smooth functions that are infinitely differentiable in the cell, and at the cell boundaries they satisfy the continuity conditions for velocity, normal and tangential stresses. Since the boundary value problem for the Laplace equation is solved, it is assumed that the solution found is unique. The type of functions allows us to separate the variables and to reduce the problem's solution to the solution of ordinary differential equations. It is found that the change in the flow rate of a fluid through a characteristic cross section is determined mainly by the geometric dimensions of the cells of the free liquid in such structures and is practically independent of the size of the plates or rods.


Author(s):  
M. Boublik ◽  
W. Hellmann ◽  
F. Jenkins

The present knowledge of the three-dimensional structure of ribosomes is far too limited to enable a complete understanding of the various roles which ribosomes play in protein biosynthesis. The spatial arrangement of proteins and ribonuclec acids in ribosomes can be analysed in many ways. Determination of binding sites for individual proteins on ribonuclec acid and locations of the mutual positions of proteins on the ribosome using labeling with fluorescent dyes, cross-linking reagents, neutron-diffraction or antibodies against ribosomal proteins seem to be most successful approaches. Structure and function of ribosomes can be correlated be depleting the complete ribosomes of some proteins to the functionally inactive core and by subsequent partial reconstitution in order to regain active ribosomal particles.


Author(s):  
Robert Glaeser ◽  
Thomas Bauer ◽  
David Grano

In transmission electron microscopy, the 3-dimensional structure of an object is usually obtained in one of two ways. For objects which can be included in one specimen, as for example with elements included in freeze- dried whole mounts and examined with a high voltage microscope, stereo pairs can be obtained which exhibit the 3-D structure of the element. For objects which can not be included in one specimen, the 3-D shape is obtained by reconstruction from serial sections. However, without stereo imagery, only detail which remains constant within the thickness of the section can be used in the reconstruction; consequently, the choice is between a low resolution reconstruction using a few thick sections and a better resolution reconstruction using many thin sections, generally a tedious chore. This paper describes an approach to 3-D reconstruction which uses stereo images of serial thick sections to reconstruct an object including detail which changes within the depth of an individual thick section.


Author(s):  
T.D. Pollard ◽  
P. Maupin

In this paper we review some of the contributions that electron microscopy has made to the analysis of actin and myosin from nonmuscle cells. We place particular emphasis upon the limitations of the ultrastructural techniques used to study these cytoplasmic contractile proteins, because it is not widely recognized how difficult it is to preserve these elements of the cytoplasmic matrix for electron microscopy. The structure of actin filaments is well preserved for electron microscope observation by negative staining with uranyl acetate (Figure 1). In fact, to a resolution of about 3nm the three-dimensional structure of actin filaments determined by computer image processing of electron micrographs of negatively stained specimens (Moore et al., 1970) is indistinguishable from the structure revealed by X-ray diffraction of living muscle.


Author(s):  
J.L. Williams ◽  
K. Heathcote ◽  
E.J. Greer

High Voltage Electron Microscope already offers exciting experimental possibilities to Biologists and Materials Scientists because the increased specimen thickness allows direct observation of three dimensional structure and dynamic experiments on effectively bulk specimens. This microscope is designed to give maximum accessibility and space in the specimen region for the special stages which are required. At the same time it provides an ease of operation similar to a conventional instrument.


Author(s):  
G. E. Tyson ◽  
M. J. Song

Natural populations of the brine shrimp, Artemia, may possess spirochete- infected animals in low numbers. The ultrastructure of Artemia's spirochete has been described by conventional transmission electron microscopy. In infected shrimp, spirochetal cells were abundant in the blood and also occurred intra- and extracellularly in the three organs examined, i.e. the maxillary gland (segmental excretory organ), the integument, and certain muscles The efferent-tubule region of the maxillary gland possessed a distinctive lesion comprised of a group of spirochetes, together with numerous small vesicles, situated in a cave-like indentation of the base of the tubule epithelium. in some instances the basal lamina at a lesion site was clearly discontinuous. High-voltage electron microscopy has now been used to study lesions of the efferent tubule, with the aim of understanding better their three-dimensional structure.Tissue from one maxillary gland of an infected, adult, female brine shrimp was used for HVEM study.


Author(s):  
Jerome J. Paulin

Within the past decade it has become apparent that HVEM offers the biologist a means to explore the three-dimensional structure of cells and/or organelles. Stereo-imaging of thick sections (e.g. 0.25-10 μm) not only reveals anatomical features of cellular components, but also reduces errors of interpretation associated with overlap of structures seen in thick sections. Concomitant with stereo-imaging techniques conventional serial Sectioning methods developed with thin sections have been adopted to serial thick sections (≥ 0.25 μm). Three-dimensional reconstructions of the chondriome of several species of trypanosomatid flagellates have been made from tracings of mitochondrial profiles on cellulose acetate sheets. The sheets are flooded with acetone, gluing them together, and the model sawed from the composite and redrawn.The extensive mitochondrial reticulum can be seen in consecutive thick sections of (0.25 μm thick) Crithidia fasciculata (Figs. 1-2). Profiles of the mitochondrion are distinguishable from the anterior apex of the cell (small arrow, Fig. 1) to the posterior pole (small arrow, Fig. 2).


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