Estimation of Critical Submergence at Single Horizontal Intakes Under Asymmetric Flow Conditions

2022 ◽  
Author(s):  
Emre Haspolat ◽  
Mustafa Gogus
Keyword(s):  
Flow Conditions ◽  
Asymmetric Flow ◽  
Critical Submergence

scholarly journals GP approach for critical submergence of intakes in open channel flows

2012 ◽  
Vol 14 (4) ◽  
pp. 937-943 ◽  
Author(s):  
H. Md. Azamathulla ◽  
Z. Ahmad
Keyword(s):  
Reynolds Number ◽  
Weber Number ◽  
Open Channel ◽  
Laboratory Data ◽  
Open Channel Flow ◽  
Flow Conditions ◽  
Open Channel Flows ◽  
Wide Range ◽  
Channel Velocity ◽  
Critical Submergence

This technical paper presents the genetic programming (GP) approach to predict the critical submergence for horizontal intakes in open channel flow for different bottom clearances. Laboratory data from the literature for the critical submergence for a wide range of flow conditions were used for the development and testing of the proposed method. Froude number, Reynolds number, Weber number and ratio of intake velocity and channel velocity were considered dominant parameters affecting the critical submergence. The proposed GP approach produced satisfactory results compared to the existing predictors.

Thrombus formation on artificial surfaces: Correlative microscopy

1990 ◽  
Vol 48 (3) ◽  
pp. 840-841
Author(s):  
Quintin J. Lai ◽  
Stuart L. Cooper ◽  
Ralph M. Albrecht
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Low Voltage ◽  
Thrombus Formation ◽  
Blood Platelets ◽  
Polymer Surfaces ◽  
Flow Conditions ◽  
Transmission Electron ◽  
Adhesion Of Platelets ◽  
Microscopic Techniques

Thrombus formation and embolization are significant problems for blood-contacting biomedical devices. Two major components of thrombi are blood platelets and the plasma protein, fibrinogen. Previous studies have examined interactions of platelets with polymer surfaces, fibrinogen with platelets, and platelets in suspension with spreading platelets attached to surfaces. Correlative microscopic techniques permit light microscopic observations of labeled living platelets, under static or flow conditions, followed by the observation of identical platelets by electron microscopy. Videoenhanced, differential interference contrast (DIC) light microscopy permits high-resolution, real-time imaging of live platelets and their interactions with surfaces. Interference reflection microscopy (IRM) provides information on the focal adhesion of platelets on surfaces. High voltage, transmission electron microscopy (HVEM) allows observation of platelet cytoskeletal structure of whole mount preparations. Low-voltage, high resolution, scanning electron microscopy allows observation of fine surface detail of platelets. Colloidal gold-labeled fibrinogen, used to identify the Gp Ilb/IIIa membrane receptor for fibrinogen, can be detected in all the above microscopies.

Hydrodynamic flow conditions through permeable walls

1992 ◽  
Vol 2 (8) ◽  
pp. 1565-1569
Author(s):  
S. Vollmar ◽  
J. A. M. S. Duarte
Keyword(s):  
Hydrodynamic Flow ◽  
Flow Conditions ◽  
Permeable Walls

Platelet and Shear Rate Promote Tumor Cell Adhesion to Human Endothelial Extracellular Matrix - Absence of a Role for Platelet Cyclooxygenase

1989 ◽  
Vol 61 (03) ◽  
pp. 485-489 ◽  
Author(s):  
Eva Bastida ◽  
Lourdes Almirall ◽  
Antonio Ordinas
Keyword(s):  
Cell Adhesion ◽  
Shear Rate ◽  
Tumor Cell ◽  
Umbilical Vein ◽  
Blood Platelets ◽  
Flow Conditions ◽  
Tumor Cell Adhesion ◽  
Rate Dependent ◽  
Static Conditions

SummaryBlood platelets are thought to be involved in certain aspects of malignant dissemination. To study the role of platelets in tumor cell adherence to vascular endothelium we performed studies under static and flow conditions, measuring tumor cell adhesion in the absence or presence of platelets. We used highly metastatic human adenocarcinoma cells of the lung, cultured human umbilical vein endothelial cells (ECs) and extracellular matrices (ECM) prepared from confluent EC monolayers. Our results indicated that under static conditions platelets do not significantly increase tumor cell adhesion to either intact ECs or to exposed ECM. Conversely, the studies performed under flow conditions using the flat chamber perfusion system indicated that the presence of 2 × 105 pl/μl in the perfusate significantly increased the number of tumor cells adhered to ECM, and that this effect was shear rate dependent. The maximal values of tumor cell adhesion were obtained, in presence of platelets, at a shear rate of 1,300 sec-1. Furthermore, our results with ASA-treated platelets suggest that the role of platelets in enhancing tumor cell adhesion to ECM is independent of the activation of the platelet cyclooxygenase pathway.

Sign in / Sign up

Export Citation Format

Share Document