4.3 Article

Investigating internal architecture effect in plastic deformation and failure for TPMS-based scaffolds using simulation methods and experimental procedure

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ELSEVIER
DOI: 10.1016/j.msec.2014.07.047

Keywords

Bone tissue engineering; TPMS based scaffolds; Failure mechanism; Deformation procedure

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Rapid prototyping (RP) has been a promising technique for producing tissue engineering scaffolds which mimic the behavior of host tissue as properly as possible. Biodegradability, agreeable feasibility of cell growth, and migration parallel to mechanical properties, such as strength and energy absorption, have to be considered in design procedure. In order to study the effect of internal architecture on the plastic deformation and failure pattern, the architecture of triply periodic minimal surfaces which have been observed in nature were used. P and D surfaces at 30% and 60% of volume fractions were modeled with 3 * 3 * 3 unit cells and imported to Objet EDEN 260 3-D printer. Models were printed by VeroBlue FullCure 840 photopolymer resin. Mechanical compression test was performed to investigate the compressive behavior of scaffolds. Deformation procedure and stress-strain curves were simulated by FEA and exhibited good agreement with the experimental observation. Current approaches for predicting dominant deformation mode under compression containing Maxwell's criteria and scaling laws were also investigated to achieve an understanding of the relationships between deformation pattern and mechanical properties of porous structures. It was observed that effect of stress concentration in TPMS-based scaffolds resultant by heterogeneous mass distribution, particularly at lower volume fractions, led to a different behavior from that of typical cellular materials. As a result, although more parameters are considered for determining dominant deformation in scaling laws, two mentioned approaches could not exclusively be used to compare the mechanical response of cellular materials at the same volume fraction. (C) 2014 Elsevier B.V. All rights reserved.

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