Performance assessment of longitudinal flow through rod bundle of ETRR-2 Cobalt/Iridium irradiation device

2021 ◽  
Vol 151 ◽  
pp. 107897
Author(s):  
Hesham Elbakhshawangy ◽  
Abdelfatah Abdelmaksoud
1998 ◽  
Vol 120 (4) ◽  
pp. 786-791 ◽  
Author(s):  
Sun Kyu Yang ◽  
Moon Ki Chung

The effects of the spacer grids with mixing vanes in rod bundles on the turbulent structure were investigated experimentally. The detailed hydraulic characteristics in subchannels of a 5 × 5 rod bundle with mixing spacer grids were measured upstream and downstream of the spacer grid by using a one component LDV (Laser Doppler Velocimetry). Axial velocity and turbulent intensity, skewness factor, and flatness factor were measured. The turbulence decay behind spacer grids was obtained from measured data. The trend of turbulence decay behaves in a similar way as turbulent flow through mesh grids or screens. Pressure drop measurements were also performed to evaluate the loss coefficient for the spacer grid and the friction factor for a rod bundle.


2011 ◽  
Vol 32 (11-12) ◽  
pp. 957-967 ◽  
Author(s):  
Smith Eiamsa-Ard ◽  
Vichan Kongkaitpaiboon ◽  
Pongjet Promvonge

In a previous paper an account of certain investigations into the physics of the flow of water through wood has been given. These experiments showed that in the wood of actively transpiring trees the total pressure required to maintain the transpiration rate of flow might amount to a head of water of from five to seven times the height of the tree. The factors which produce this resistance are the friction against the sides of the vessels, the passage through the end walls, and the special highly variable resistance due to the presence of air bubbles in the vessels. Other things being equal, the resistance to flow is strictly proportional to the length of the stem, provided that the conducting tract is approximately similar in character and in sectional area throughout the length of the piece of stem tested. Hence it is difficult to see any reason for Curtis’s statement that the resistance offered by a stem to the flow of water is not proportional to the length of the stem, unless this observer worked with partially blocked stems. This author also states that the same force is required to overcome the resistance to a definite rate of flow, whether applied as a pressure or as a tension. This is, however, only the case when the conducting elements are completely filled with water, and even then the resistance to flow is two or three times greater than would be expected from a viscosity calculation. The latter fact is partly due to the internal thickenings on the vessels, which reduce their effective radius, and partly to the existence of transverse partitions in long pieces of stem, which add to the resistance to longitudinal flow. The average resistance to flow through the side wall of a vessel or through that of a tracheide of a Conifer may be from 2 to 10 or more times the resistance to flow through the entire length of the same vessel when filled with water, although when large numbers of air bubbles are present the tendency to lateral exudation from a given longitudinal path is much increased. In this way water can be transmitted rapidly and with but little lateral exudation through tracts where the supply is abundant and the local demand small, so that the vessels are filled, whereas in a region where the loss by transpiration is excessive, the appearance of air bubbles in the vessels partially blocks the upward flow and increases the lateral exudation until the local needs are supplied. Strasburger attempted to show that the flow of fluids through the vessels of wood was dependent upon their viscosity, by driving such liquids as water, turpentine, alcohol, ether, and benzole through short lengths of stem under similar heads and noting the time of formation of a drop in each case. Strasburger’s method is vitiated by his assumption that the drops of the different liquids were of the same size, which is not the case, and he also forgets that the different densities of the liquids cause the weight of the columns in the vessels to vary. Nevertheless he found that the number of drops passing through in a given time was approximately proportional to the viscosity of the liquids used. As a matter of fact, the values obtained for the viscosity by this method depend largely upon the order in which the different liquids are passed through the stem, even when the actual volume escaping is measured. Thus water preceding turpentine or benzole gives absurdly different results to water following these liquids, and to a less extent the same applies with alcohol and ether. The relation between flow and viscosity can be best shown by comparing the flow of water at different temperatures, as has already been done.


1972 ◽  
Vol 94 (2) ◽  
pp. 169-173 ◽  
Author(s):  
Chia-Jung Hsu

Heat transfer in longitudinal laminar flow through tightly packed rod bundles is analyzed for a rod displaced from its symmetrical position. The influences of the P/D ratio, the magnitude of σ, and the type of thermal boundary condition, etc. on the variation of the coolant temperature field and the rod-average Nusselt number are investigated. Average Nusselt numbers for the displaced rod are calculated for rod bundles with 1.00 ≤ P/D ≤ 2.0 and 0 ≤ σ ≤ 0.8. The results for the special case of σ = 0 (i.e., for symmetrical rod bundle) show excellent agreement with those reported by Dwyer and Berry [1], who analyzed numerically the corresponding problem for symmetrical rod bundles.


1971 ◽  
Vol 49 (5) ◽  
pp. 717-733 ◽  
Author(s):  
J. A. Webb

14C translocation through the node ceases immediately the tissue is chilled (0°) and 14C export from the blade is considerably reduced within the next 5 min, while the assimilation rate remains unchanged. The ratio of 14C distribution among the translocated compounds indicates a uniform deceleration of the entire longitudinal flow through the unchilled length of petiole. Immediately after node chilling an increasing restraint is imposed on the rate of 14C translocation throughout the length of the petiole. This second inhibitory effect of cold treatment is maximally expressed between 30 and 60 min after node chilling and may reflect an accentuated accumulation of translocates within the phloem under these conditions. Translocation through the node resumes immediately the tissue is returned to 25°. Initially the rate is slow but within 90 min of warming the node, when all prechilling restraints on longitudinal movement appear to be removed, the rate of 14C translocation approaches that of control plants. Rapid resumption of transport through the node is matched by a rapid loss of 14C from the blade, again indicating that the entire longitudinal flow moves as a continuum. The longitudinal transport in the phloem and radial movement into the surrounding tissues are both rapidly inhibited at 0 °C. Longitudinal movement will acclimate and within 6 h of continuous cold (1 °C) appreciable transport is resumed through the chilled zone while after 19 to 20 h almost complete recovery of translocation is achieved. There was no evidence for acclimation of the radial movement. If radial movement of 14C reflects cytoplasmic streaming then longitudinal movement likely proceeds by some other mechanism. An evaluation of the extensive cytological observations of phloem tissue produced no clues to explain the mechanism of low temperature inhibition of translocation at the structural level.


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