Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 25 (1987), S. 12-17 
    ISSN: 1741-0444
    Keywords: Arteries ; Atherosclerosis ; Bifucations ; Branches ; Haemodynamics ; Marker and cell ; Trunk
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Atherosclerosis is known to be localised in arterial bends, bifurcations and branches. The exact mechanism is not known but it appears that the process starts due to haemodynamic changes. In general, the distribution arteries have relatively symmetrical bifurcations with varying angles and branch trunk area ratios. Several previously studied flow related characteristics were dependent on Reynolds number, angle of bifurcation and area ratios. The time dependence nature of the flow was not included in the above investigations. The equations of continuity and motion for two dimensional, time dependent flow of a homogenous, incompressible fluid through a horizontal, bifurcating rigid channel were therefore solved. The numerical method chosen to solve this problem was the marker and cell (MAC) method, which enabled the two velocity components and the pressure to be obtained directly. According to this system the flow field was divided into cells rather than points according to a prescribed scheme. It was found that a high shear stress zone developed at the daughter’s medial wall while at the lateral wall the fluid tends to follow the pressure gradient and the flow was reversed for part of the cycle. In addition, a high pressure zone which could attain values of twice the input pressure was found on the medial wall.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...