SinoGreenTech Academic Portal
Official PDF TranslationSCIENCE CHINA Materials

Advances toward stress-assisted degradation of biomedical Mg alloys

Authors: XU Daoxiang; JIANG Xueqi; DING Junjie; ZHOU Xingxing; QIAN Kun; BA Zhixin; ZHANG Xiaobo; BAI Jing; YAN Kai; DONG Qiangsheng

DOI: 10.1007/s40843-026-4426-yStatus: Verified Translated Edition
Sponsored AdvertisementAd Placement Area
reCAPTCHA Bot Shield Active

Preparing Secure Academic Download

Verifying human reader & generating high-resolution document...

Verifying Document Integrity15s remaining
← Back to Article
Protected by Google reCAPTCHA v3.PrivacyTerms
Sponsored ContentAdSense In-Feed Ad Slot

Key Findings in This Report

• • Corrosion fatigue in 5% NaCl reduces the fatigue strength of extruded AZ80-T5 and AZ31 Mg alloys by 40–70% compared with air, with fatigue limits falling to 40–70 MPa at 10^7 cycles; this premature mechanical failure directly threatens the structural integrity of load-bearing orthopedic implants and cardiovascular stents. • • Flow-induced shear stress exceeding approximately 1 Pa in microfluidic and cardiovascular test systems disrupts the passivation film on Mg alloys, increasing degradation rates by up to 3-fold relative to static immersion; this threshold defines the hydrodynamic condition under which stent struts and flow-exposed implants lose mass at clinically unacceptable rates. • • Phase-field and peridynamic models capture pit-to-crack transitions in biodegradable Mg alloys with damage localization driven by secondary phases, enabling prediction of SCC initiation sites at the micrometer scale; such models reduce reliance on costly and time-consuming in vivo trials during alloy screening. • • Surface treatments including plasma electrolytic oxidation (PEO) on AZ61 Mg alloy alter fatigue performance, with PEO coatings introducing brittle layers that can reduce fatigue life by 20–50% depending on coating thickness and defect density; this trade-off between corrosion protection and fatigue resistance must be resolved for clinical adoption.