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Development of a test method to investigate mode II fracture and dissection of arteries.

Authors :
FitzGibbon, Brian
McGarry, Patrick
Source :
Acta Biomaterialia; Feb2021, Vol. 121, p444-460, 17p
Publication Year :
2021

Abstract

The current study presents the development and implementation of a bespoke experimental technique to generate and characterise mode II crack initiation and propagation in arterial tissue. The current study begins with a demonstration that lap-shear testing of arterial tissue results in mixed mode fracture, rather than mode II. We perform a detailed computational design of a bespoke experimental method (which we refer to as a shear fracture ring test (SFRT)) to robustly and repeatably generate mode II crack initiation and propagation in arteries. This method is based on generating a localised region of high shear adjacent to a cylindrical loading bar. Placement of a radial notch in this region of high shear stress is predicted to result in a kinking of the crack during a mode II initiation and propagation of the crack over a long distance in the circumferential (c)- direction along the circumferential-axial (c-a) plane. Fabrication and experimental implementation of the SFRT on excised ovine aorta specimens confirms that the bespoke test method results in pure mode II initiation and propagation. We demonstrate that the mode II fracture strength along the c-a plane is eight times higher than the corresponding mode I strength determined from a standard peel test. We also calibrate the mode II fracture energy based on our measurement of crack propagation rates. The mechanisms of fracture uncovered in the current study, along with our quantification of mode II fracture properties have significant implications for current understanding of the biomechanical conditions underlying aortic dissection. Image, graphical abstract [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17427061
Volume :
121
Database :
Supplemental Index
Journal :
Acta Biomaterialia
Publication Type :
Academic Journal
Accession number :
148334955
Full Text :
https://doi.org/10.1016/j.actbio.2020.11.023