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Anodization Mechanism on SiC Nanoparticle Reinforced Al Matrix Composites Produced by Power Metallurgy

机译:动力冶金生产SiC纳米颗粒增强Al基复合材料的阳极氧化机理

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摘要

Specimens of aluminum-based composites reinforced by silicon carbide nanoparticles (Al/SiCnp) produced by powder metallurgy (PM) were anodized under voltage control in tartaric-sulfuric acid (TSA). In this work, the influence of the amount of SiCnp on the film growth during anodizing was investigated. The current density versus time response and the morphology of the porous alumina film formed at the composite surface are compared to those concerning a commercial aluminum alloy (AA1050) anodized under the same conditions. The processing method of the aluminum alloys influences the efficiency of the anodizing process, leading to a lower thicknesses for the unreinforced Al-PM alloy regarding the AA1050. The current density versus time response is strongly dependent on the amount of SiCnp. The current peaks and the steady-state current density recorded at each voltage step increases with the SiCnp volume fraction due to the oxidation of the SiCnp. The formation mechanism of the anodic film on Al/SiCnp composites is different from that occurring in AA1050, partly due the heterogeneous distribution of the reinforcement particles in the metallic matrix, but also to the entrapment of SiCnp in the anodic film.
机译:在电压控制下,在酒石酸(TSA)中对由粉末冶金(PM)生产的由碳化硅纳米颗粒(Al / SiCnp)增强的铝基复合材料进行阳极氧化。在这项工作中,研究了SiCnp量对阳极氧化过程中膜生长的影响。将在复合表面上形成的多孔氧化铝膜的电流密度随时间变化的响应和形态与在相同条件下阳极氧化的商用铝合金(AA1050)进行了比较。铝合金的加工方法会影响阳极氧化工艺的效率,从而导致AA1050的未增强Al-PM合金的厚度降低。电流密度与时间响应的关系主要取决于SiCnp的数量。由于SiCnp的氧化,每个电压阶跃处记录的电流峰值和稳态电流密度随SiCnp体积分数的增加而增加。 Al / SiCnp复合材料上阳极膜的形成机理与AA1050中的阳极膜形成机理不同,部分原因是增强颗粒在金属基体中的分布不均匀,而且还由于SiCnp截留在阳极膜中。

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