在这项工作中,纯Mg的腐蚀行为,Mg3Ag,Mg6Ag,和MgZnYNd合金在不同的固定剂(乙醇(EA),85%乙醇(85%EA),10%中性缓冲福尔马林(10%NBF),4%戊二醛(4%GD),4%多聚甲醛(4%PFA)的研究,为镁种植体组织学评价中固定剂的选择提供有价值的参考。通过析氢试验,pH测试,和腐蚀形态和产品表征,发现EA和85%EA组中的腐蚀进展最慢,在4%GD中略快,在10%NBF中更快,最快的是4%的PFA。腐蚀后,EA组表面保持不变,而85%的EA组表面出现较小的裂纹和翘曲。4%GD固定剂在Mg基体上形成致密的针状保护层。10%NBF组最初生长均匀一层,但后来由于加速腐蚀而形成不规则的凹坑。相比之下,4%PFA溶液引起更严重的由氯离子引起的腐蚀。EA和85%EA组中的主要腐蚀产物是MgO和Mg(OH)2,而其他包含不同离子的固定剂也产生磷酸盐,例如Mg3(PO4)2和MgHPO4。在4%的PFA中,腐蚀后在Mg6Ag合金表面形成AgCl。因此,在不影响染色质量的情况下最大限度地减少镁合金腐蚀,建议使用EA或85%EA,而4%的PFA由于其显著影响而不推荐。
In this work, the corrosion behavior of pure Mg, Mg3Ag, Mg6Ag, and MgZnYNd alloys in different fixatives (ethyl alcohol (EA), 85 % ethyl alcohol (85 % EA), 10 % neutral buffered formalin (10 % NBF), 4 % glutaric dialdehyde (4 % GD), and 4 % paraformaldehyde (4 % PFA)) was investigated to provide a valuable reference for the selection of fixatives during the histological evaluation of Mg implants. Through the hydrogen evolution test, pH test, and corrosion morphology and product characterization, it was found that corrosion proceeded slowest in the EA and 85 % EA groups, slightly faster in 4 % GD, faster in 10 % NBF, and fastest in 4 % PFA. After corrosion, the EA group surface remained unchanged, while the 85%EA group surface developed minor cracks and warping. The 4%GD fixative formed a dense needle-like protective layer on the Mg substrate. The 10%NBF group initially grew a uniform layer, but later developed irregular pits due to accelerated corrosion. In contrast, the 4%PFA solution caused more severe corrosion attributed to chloride ions. The main corrosion products in the EA and 85%EA groups were MgO and Mg(OH)2, while the other fixatives containing diverse ions also yielded phosphates like Mg3(PO4)2 and MgHPO4. In 4 % PFA, AgCl formed on the surface of Mg6Ag alloy after corrosion. Therefore, to minimize Mg alloy corrosion without compromising staining quality, EA or 85 % EA is recommended, while 4 % PFA is not recommended due to its significant impact.