Effect of rolling friction on wall pressure, discharge velocity and outflow of granular material from a flat-bottomed bin

Particuology ◽  
2012 ◽  
Vol 10 (6) ◽  
pp. 672-682 ◽  
Author(s):  
R. Balevičius ◽  
I. Sielamowicz ◽  
Z. Mróz ◽  
R. Kačianauskas
1994 ◽  
Vol 116 (2) ◽  
pp. 370-373 ◽  
Author(s):  
Hui Li ◽  
Yuji Tomita

This paper examines experimentally the decay of swirl, the average dynamic, static and total pressures and the wall pressure in a pipeline 13 m in length and with an inside diameter of 80 mm for two Reynolds numbers and five different inlet swirls. The empirical correlations for the above quantities are derived, and by using these empirical correlations, the decay process and pressure distributions along the pipe for the swirling flow can be successfully computed by giving discharge velocity and a wall static pressure at any axial position.


2020 ◽  
Vol 2020 ◽  
pp. 1-14
Author(s):  
Yong Feng ◽  
Caihua Yu ◽  
Fan Pan

The evolution mechanism of discharge velocity profiles and force chain distribution of maize particles in silos was studied based on the interaction between internal and external rolling friction of particles. Through EDEM, the silo and maize grain models were established for unloading simulation, whose flow pattern was compared with the silo unloading test to verify the rationality of the simulation. By slice observation, we compared and analyzed the time evolution rules of particle mesoscopic parameters under different friction conditions. The results show that the larger the interparticle friction coefficient is, the longer the total discharge time is and the smaller the coefficient of rolling friction between particles, the earlier the particle flow from mass flow to funnel flow. For silos with the funnel, the reduction of interparticle friction will change the limit between the mass flow and the funnel flow, thus increasing the area of the funnel flow. When the coefficient of rolling friction increases, the vertical velocity and angular velocity of the particle near the silo middle increase. However, the effects of internal and external friction coupling on the vertical velocity of the side particle, the horizontal velocity of the whole particle, and the spatial distribution and probability distribution of the force chain are more significant.


Author(s):  
Joachim R. Sommer ◽  
Nancy R. Wallace

After Howell (1) had shown that ruthenium red treatment of fixed frog skeletal muscle caused collapse of the intermediate cisternae of the sarcoplasmic reticulum (SR), forming a pentalaminate structure by obi iterating the SR lumen, we demonstrated that the phenomenon involves the entire SR including the nuclear envelope and that it also occurs after treatment with other cations, including calcium (2,3,4).From these observations we have formulated a hypothesis which states that intracellular calcium taken up by the SR at the end of contraction causes the M rete to collapse at a certain threshold concentration as the first step in a subsequent centrifugal zippering of the free SR toward the junctional SR (JSR). This would cause a) bulk transport of SR contents, such as calcium and granular material (4) into the JSR and, b) electrical isolation of the free SR from the JSR.


Author(s):  
Awtar Krishan ◽  
Dora Hsu

Cells exposed to antitumor plant alkaloids, vinblastine and vincristine sulfate have large proteinacious crystals and complexes of ribosomes, helical polyribosomes and electron-dense granular material (ribosomal complexes) in their cytoplasm, Binding of H3-colchicine by the in vivo crystals shows that they contain microtubular proteins. Association of ribosomal complexes with the crystals suggests that these structures may be interrelated.In the present study cultured human leukemic lymphoblasts (CCRF-CEM), were incubated with protein and RNA-synthesis inhibitors, p. fluorophenylalanine, puromycin, cycloheximide or actinomycin-D before the addition of crystal-inducing doses of vinblastine to the culture medium. None of these compounds could completely prevent the formation of the ribosomal complexes or the crystals. However, in cells pre-incubated with puromycin, cycloheximide, or actinomycin-D, a reduction in the number and size of the ribosomal complexes was seen. Large helical polyribosomes were absent in the ribosomal complexes of cells treated with puromycin, while in cells exposed to cycloheximide, there was an apparent reduction in the number of ribosomes associated with the ribosomal complexes (Fig. 2).


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