...
【24h】

The use of electrochemical hydrogen permeation techniques to detect hydride phase separation in amorphous metallic alloys

机译:使用电化学氢渗透技术检测非晶态金属合金中的氢化物相分离

获取原文
获取原文并翻译 | 示例
           

摘要

Samples of amorphous Fe40Ni38Mo4B18 and Ni81P19 alloys were submitted to electrochemical hydrogen permeation tests, under cathodic charging conditions, which resulted in elevated hydrogen fugacity. Two different permeation techniques were used: the double-potentiostatic and the potentiostatic step methods. The main difference between these techniques is the form of the resulting hydrogen concentration profile across the sample thickness. The hydrogen permeation curves for the Ni81P19 samples, for both techniques, had shapes identical to the theoretical curves. The experimental curves for the Fe40Ni38Mo4B18 samples, however, deviated from the theoretical curves. These deviations are attributed to the formation of a hydride phase due to the high hydrogen fugacity imposed during cathodic charging. The potential use of these electrochemical hydrogen permeation techniques is demonstrated in the study of phase separation through the analysis of the growth of a new phase. The diffusivity of hydrogen in the hydride formed in the Fe40Ni38Mo4B18 amorphous metallic alloy was found to be 5.7 +/- 0.3 x 10(-15) m(2) s(-1) and the thickness of the hydride layer, formed during the double-potentiostatic test, for a cathodic charging level of -2000 mV/SCE saturated calomel electrode (SCE) was found to be 18.9 +/- 0.5 mu m. (C) 1998 Published by Elsevier Science B.V. All rights reserved. [References: 14]
机译:非晶态Fe40Ni38Mo4B18和Ni81P19合金的样品在阴极充电条件下进行了电化学氢渗透测试,导致氢逸度提高。使用了两种不同的渗透技术:双恒电位和恒电位步进法。这些技术之间的主要区别是整个样品厚度上所得氢浓度分布的形式。对于这两种技术,Ni81P19样品的氢渗透曲线均具有与理论曲线相同的形状。但是,Fe40Ni38Mo4B18样品的实验曲线偏离了理论曲线。这些偏差归因于由于在阴极充电期间施加的高氢逸度而形成的氢化物相。通过分析新相的生长,在相分离的研究中证明了这些电化学氢渗透技术的潜在用途。发现在Fe40Ni38Mo4B18非晶态金属合金中形成的氢化物中氢的扩散率为5.7 +/- 0.3 x 10(-15)m(2)s(-1)和在两次加氢过程中形成的氢化物层的厚度-恒电位测试,对于-2000mV / SCE的饱和甘汞电极(SCE)的阴极充电水平为18.9 +/-0.5μm。 (C)1998,Elsevier Science B.V.保留所有权利。 [参考:14]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号