Simulations of Electrospray in a Colloid Thruster with a High Resolution Three-dimensional Particle-in-Cell Model

Author(s):  
Pengxiang Wang ◽  
Arnaud Borner ◽  
Zheng Li ◽  
Deborah A. Levin
Symmetry ◽  
2022 ◽  
Vol 14 (1) ◽  
pp. 170
Author(s):  
Panayiotis Vafeas ◽  
Eleftherios Protopapas ◽  
Maria Hadjinicolaou

Modern engineering technology often involves the physical application of heat and mass transfer. These processes are associated with the creeping motion of a relatively homogeneous swarm of small particles, where the spheroidal geometry represents the shape of the embedded particles within such aggregates. Here, the steady Stokes flow of an incompressible, viscous fluid through an assemblage of particles, at low Reynolds numbers, is studied by employing a particle-in-cell model. The mathematical formulation adopts the Kuwabara-type assumption, according to which each spheroidal particle is stationary and it is surrounded by a confocal spheroid that creates a fluid envelope, in which the Newtonian fluid moves with a constant velocity of arbitrary orientation. The boundary value problem in the fluid envelope is solved by imposing non-slip conditions on the surface of the spheroid, which is also considered as non-penetrable, while zero vorticity is assumed on the fictitious spheroidal boundary along with a uniform approaching velocity. The three-dimensional flow fields are calculated analytically for the first time, in the spheroidal geometry, by virtue of the Papkovich–Neuber representation. Through this, the velocity and the total pressure fields are provided in terms of a vector and the scalar spheroidal harmonic potentials, which enables the thorough study of the relevant physical characteristics of the flow fields. The newly obtained analytical expressions generalize to any direction with the existing results holding for the asymmetrical case, which were obtained with the aid of a stream function. These can be employed for the calculation of quantities of physical or engineering interest. Numerical implementation reveals the flow behavior within the fluid envelope for different geometrical cell characteristics and for the arbitrarily-assumed velocity field, thus reflecting the different flow/porous media situations. Sample calculations show the excellent agreement of the obtained results with those available for special geometrical cases. All of these findings demonstrate the usefulness of the proposed method and the powerfulness of the obtained analytical expansions.


2018 ◽  
Vol 25 (6) ◽  
pp. 061208 ◽  
Author(s):  
Francesco Taccogna ◽  
Pierpaolo Minelli

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):  
Kenneth H. Downing ◽  
Hu Meisheng ◽  
Hans-Rudolf Went ◽  
Michael A. O'Keefe

With current advances in electron microscope design, high resolution electron microscopy has become routine, and point resolutions of better than 2Å have been obtained in images of many inorganic crystals. Although this resolution is sufficient to resolve interatomic spacings, interpretation generally requires comparison of experimental images with calculations. Since the images are two-dimensional representations of projections of the full three-dimensional structure, information is invariably lost in the overlapping images of atoms at various heights. The technique of electron crystallography, in which information from several views of a crystal is combined, has been developed to obtain three-dimensional information on proteins. The resolution in images of proteins is severely limited by effects of radiation damage. In principle, atomic-resolution, 3D reconstructions should be obtainable from specimens that are resistant to damage. The most serious problem would appear to be in obtaining high-resolution images from areas that are thin enough that dynamical scattering effects can be ignored.


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