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Synthesis of alpha-aluminum oxide and hydrogen fluoride-doped beta-nickel aluminide coatings on single crystal nickel-based superalloy by chemical vapor deposition.

机译:通过化学气相沉积法在单晶镍基高温合金上合成α-氧化铝和氟化氢掺杂的β-镍铝化物涂层。

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Thermal barrier coatings (TBCs) are widely used for air-cooled turbine components in advanced aircraft engines and power generation systems. The dominant failure mode observed in TBCs is progressive fracture of the metal-oxide interface upon oxidation and thermal cycling. Two potential coating methods for improving TBC performance were studied: (1) preparing a high-quality α-Al 2O3 coating layer on the surface of a single crystal Ni-based superalloy (René N5) to extend the oxidative stability of the interface and (2) doping β-NiAl bond coating with a small amount of Hf to improve the adhesion of thermally grown oxide (TGO) at the interface.; In the first coating method, a novel chemical vapor deposition (CVD) procedure was developed using AlCl3, CO2 and H 2 as precursors. A critical part of this procedure was a short-time pre-oxidation step (1 min) with CO2 and H2 in the CVD chamber, prior to introducing the AlCl3, vapor. Without this pre-oxidation step, extensive whisker formation was observed on the alloy surface. Characterization results showed that the pre-oxidation step resulted in the formation of a continuous oxide layer (∼50 nm) on the alloy surface. The outer part of this layer (∼20 nm) appeared to contain mixed oxides whereas the inner part (∼30 nm) consisted of α-Al2O3 as a dominant major phase and &thetas;-Al2O3 as a minor phase. It appeared that the preferential nucleation of β-Al2O3 in the pre-oxidized layer was promoted by: (1) rapid heating (∼10 sec) of the alloy surface to the temperature region, where α-Al 2O3 was expected to nucleate instead of metastable Al 2O3 phases, (2) the low oxygen pressure environment of the pre-oxidation step which kept the rate of oxidation low, and (3) contamination of the CVD chamber with HfCl4. It appeared that the role of HfCl 4 was to enhance the preferential nucleation of α-Al2O 3 in the pre-oxidized layer.; In our second coating method, we utilized the dynamic versatility of CVD as an avenue to proactively control the concentration and distribution of Hf as a beneficial dopant in the aluminide coating matrix. A laboratory-scale, hot-wall CVD reactor was specifically constructed to perform critical Hf doping experiments through “continuous” and “sequential” doping procedures. The continuous doping procedure, in which HfCl4 and AlCl3 were simultaneously introduced with H2, required a relatively high HfCl4 concentration in the gas phase to incorporate an average Hf concentration of ∼0.1 wt% in the β-NiAl coating matrix. (Abstract shortened by UMI.)
机译:隔热涂层(TBC)广泛用于高级飞机发动机和发电系统中的风冷涡轮机部件。在TBC中观察到的主要失效模式是在氧化和热循环时金属-氧化物界面的逐渐断裂。研究了两种改善TBC性能的潜在涂层方法:(1)在单晶Ni-表面上制备高质量的α-Al 2 O 3 涂层基超合金(RenéN5)来扩展界面的氧化稳定性,以及(2)用少量Hf掺杂β-NiAl键合涂层,以改善热生长氧化物(TGO)在界面上的附着力。在第一种涂覆方法中,以AlCl 3 ,CO 2 和H 2 为前体,开发了一种新的化学气相沉积(CVD)工艺。该程序的关键部分是在引入AlCl <2之前,在CVD室中用CO 2 和H 2 进行短时间的预氧化步骤(1分钟)。 sub> 3 ,蒸气。没有该预氧化步骤,在合金表面上观察到大量晶须形成。表征结果表明,预氧化步骤导致在合金表面上形成连续的氧化物层(〜50 nm)。该层的外部(〜20 nm)似乎含有混合氧化物,而内部(〜30 nm)则以α-Al 2 O 3 为主主相和-Al 2 O 3 作为次要相。似乎预氧化层中的β-Al 2 O 3 的优先成核是通过(1)快速加热(〜10秒)合金而促进的表面到温度区域,预期α-Al 2 O 3 会成核,而不是亚稳的Al 2 O 3 sub>相,(2)预氧化步骤的低氧气压力环境使氧化速率保持较低,(3)HfCl 4 污染CVD室。似乎HfCl 4 的作用是增强预氧化层中α-Al 2 O 3 的优先成核。在我们的第二种涂层方法中,我们利用CVD的动态多功能性作为主动控制铝化物涂层基质中作为有益掺杂剂的Hf的浓度和分布的途径。专门建造了实验室规模的热壁CVD反应器,以通过“连续”和“顺序”掺杂程序执行关键的Hf掺杂实验。将HfCl 4 和AlCl 3 与H 2 同时引入的连续掺杂过程需要相对较高的HfCl 4 <在气相中的浓度使β-NiAl涂层基体中的平均Hf浓度达到〜0.1 wt%。 (摘要由UMI缩短。)

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