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Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation

Alterations to the bone structure from cycle loadings can undermine its damage resistance at multiple scales. The accumulation of fatigue damage in a bone is commonly characterized by the reduction in the elastic modulus. In this study, nano-indentation was used for investigating microscopic damage...

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Detalles Bibliográficos
Autores principales: Meng, Xianjia, Qu, Chuanyong, Fu, Donghui, Qu, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231503/
https://www.ncbi.nlm.nih.gov/pubmed/34204688
http://dx.doi.org/10.3390/ma14123252
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author Meng, Xianjia
Qu, Chuanyong
Fu, Donghui
Qu, Chuan
author_facet Meng, Xianjia
Qu, Chuanyong
Fu, Donghui
Qu, Chuan
author_sort Meng, Xianjia
collection PubMed
description Alterations to the bone structure from cycle loadings can undermine its damage resistance at multiple scales. The accumulation of fatigue damage in a bone is commonly characterized by the reduction in the elastic modulus. In this study, nano-indentation was used for investigating microscopic damage evolution of bovine tibia samples subjected to fatigue loading. Indentation tests were conducted in the same 60 μm × 120 μm area with different degrees of damage, including fracture, and the evolution of reduced modulus was observed. The results showed that bone’s reduced modulus decreased significantly during the initial 40% of the life fraction, whereas it proceeded slowly during the remaining period. As the size of the residual indentations was about 4 μm in length, the degradation of bone’s reduced modulus reflected the accumulation of fatigue damage at smaller scales.
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spelling pubmed-82315032021-06-26 Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation Meng, Xianjia Qu, Chuanyong Fu, Donghui Qu, Chuan Materials (Basel) Article Alterations to the bone structure from cycle loadings can undermine its damage resistance at multiple scales. The accumulation of fatigue damage in a bone is commonly characterized by the reduction in the elastic modulus. In this study, nano-indentation was used for investigating microscopic damage evolution of bovine tibia samples subjected to fatigue loading. Indentation tests were conducted in the same 60 μm × 120 μm area with different degrees of damage, including fracture, and the evolution of reduced modulus was observed. The results showed that bone’s reduced modulus decreased significantly during the initial 40% of the life fraction, whereas it proceeded slowly during the remaining period. As the size of the residual indentations was about 4 μm in length, the degradation of bone’s reduced modulus reflected the accumulation of fatigue damage at smaller scales. MDPI 2021-06-12 /pmc/articles/PMC8231503/ /pubmed/34204688 http://dx.doi.org/10.3390/ma14123252 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Meng, Xianjia
Qu, Chuanyong
Fu, Donghui
Qu, Chuan
Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation
title Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation
title_full Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation
title_fullStr Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation
title_full_unstemmed Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation
title_short Effects of Fatigue Damage on the Microscopic Modulus of Cortical Bone Using Nanoindentation
title_sort effects of fatigue damage on the microscopic modulus of cortical bone using nanoindentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231503/
https://www.ncbi.nlm.nih.gov/pubmed/34204688
http://dx.doi.org/10.3390/ma14123252
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