腐蚀
材料科学
合金
镁合金
电化学
体内
降级(电信)
镁
特里斯
生理盐水
化学工程
冶金
无机化学
化学
生物化学
生物
电极
内分泌学
物理化学
生物技术
工程类
电信
计算机科学
作者
Lingyu Li,Bin Liu,Shuoqi Li,Fen Zhang,Yuhong Zou,Hongwei Jiang,Xiaobo Chen,Shaokang Guan,Qingyun Liu
标识
DOI:10.1007/s11706-018-0424-1
摘要
Biodegradable Mg alloys have generated great interest for biomedical applications. Accurate predictions of in vivo degradation of Mg alloys through cost-effective in vivo evaluations require the latter to be conducted in an environment close to that of physiological scenarios. However, the roles of glucose and buffering agents in regulating the in vivo degradation performance of Mg alloys has not been elucidated. Herein, degradation behavior of AZ31 alloy is investigated by hydrogen evolution measurements, pH monitoring and electrochemical tests. Results indicate that glucose plays a content-dependent role in degradation of AZ31 alloy in buffer-free saline solution. The presence of a low concentration of glucose, i.e. 1.0 g/L, decreases the corrosion rate of Mg alloy AZ31, whereas the presence of 2.0 and 3.0 g/L glucose accelerates the corrosion rate during long term immersion in saline solution. In terms of Tris-buffered saline solution, the addition of glucose increases pH value and promotes pitting corrosion or general corrosion of AZ31 alloy. This study provides a novel perspective to understand the bio-corrosion of Mg alloys in buffering agents and glucose containing solutions.
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