氧化薄膜的局部分解由化物
Eirini Lappa1, Kyriaki Saltidou1, Chrysanthi Gkili1
1Department of Chemistry, Aristotle University of Thessaloniki, University Campus, Thessaloniki, 54124, Greece.
Chemistry (Weinheim an der Bergstrasse, Germany)
|May 1, 2025
概括
(Nb) 的被动化在化物溶液中分解,导致孔腐蚀,与化物溶液不同. 这种局部腐蚀与氧化膜内的化物吸收和缺陷凝结有关,正如点缺陷模型所解释的那样.
科学领域:
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
- 腐蚀科学 腐蚀科学
背景情况:
- (Nb) 形成一个被动的氧化膜,对其耐腐蚀性至关重要.
- 了解被动薄膜的稳定性对于在侵略性环境中的材料应用至关重要.
- 局部腐蚀,如坑,仍然是许多金属和合金的一个重大挑战.
研究的目的:
- 在水性化物介质中研究Nb上的阳极氧化物被动薄膜的稳定性和分解机制.
- 为了比较Nb在化物与化物溶液中的行为.
- 用点缺陷模型阐明化物诱导局部腐蚀的物理化学过程.
主要方法:
- 在水性化物溶液中,潜在动力极化高达12VSCE.
- 不同的化物度和潜在的扫描速度.
- 使用点缺陷模型 (PDM) 进行分析.
主要成果:
- 被动Nb在化物介质中表现出局部分解 (转移稳定或稳定插孔),取决于度和扫描速率.
- 在侵略性的化物介质中,Nb保持被动性,对化物表现出不寻常的敏感性.
- 对于化物诱导的孔腐蚀,确定了临界分解潜力 (Eb).
- 实验数据与与胺活性和扫描速率相关的Eb的PDM预测一致.
结论:
- 的被动膜异常容易受到化物诱导的局部分解,与其在化物中的稳定性形成鲜明对比.
- 分解机制涉及氧化物电解质接口的化物吸收和随后的空隙凝结在Nb氧化物接口.
- 点缺陷模型有效地解释了观察到的现象,并预测了故障潜力和环境因素之间的关系.
相关概念视频
Hydroboration-Oxidation of Alkenes
7.6K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
7.6K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
1.7K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.7K
Radical Substitution: Allylic Bromination
4.8K
In organic synthesis, the formation of products can be altered by changing the reaction conditions. For example, a dibromo addition product is formed when propene is treated with bromine at room temperature. In contrast, propene undergoes allylic substitution in non-polar solvents at high temperatures to give 3-bromopropene. In order to avoid the addition reaction, the bromine concentration must be kept as low as possible throughout the reaction. This can be achieved using...
4.8K


