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The effect of aqueous phase inhibitors on mitigating potential-dependent hydrogen environments assisted cracking of an ultra-high strength steel.

机译:水相抑制剂对缓解依赖于电位的氢环境的影响有助于超高强度钢的开裂。

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摘要

Low alloy ultra-high strength alloy steel (UHSS) suffer from hydrogen environment assisted cracking (HEAC) limiting their use in marine environments. Minimum HEAC susceptibility is observed at intermediate potentials. Models explain this by a reduction in crack tip diffusible hydrogen concentration (CH,diff), enhancing threshold stress intensity (KTH) and reducing stage-II crack growth rate (da/dtII). This research seeks to extend the reduced HEAC susceptibility region by reducing C H,diff using aqueous-phase inhibitors.;A multi-facetted approach was used to quantitatively study the effect of inhibitors on reducing CH,diff. Initial tests were conducted on planar electrodes in molybdate solutions at anodic potentials and in cerium solutions at cathodic potentials; however, rescaled crevices of larger dimensions were used to measure local potential and pH as a function of applied potentials and crevice dimensions. H-uptake models were used to predict local C H,diff as a function of local potential, pH and scaling factor in the anodic and cathodic tests. Micro-mechanical models were used to predict the effects of inhibition on HEAC susceptibility. Results were related to real-size cracks using scaling factors. Last, fracture experiments were undertaken to verify predicted KTH and da/dtII obtained from the integrated investigation approach.;The addition of molybdate reduced da/dtII to 1 nm/s, expanding the reduced HEAC region to more anodic potentials. The enhanced mitigation was possibly due to forming a surface film more resistant to crack tip dissolution in addition to molybdate-induced chemical buffering of acidification both leading to reduced CH,diff. The addition of cerium reduced da/dt II to 9 and 32 nm/s at etaH = -0.35 and -0.47 V, respectively, compared to 50 and 500 nm/s at similar cathodic conditions in uninhibited tests. Cerium chemically forms an insoluble film that can reduce CH,diff by reducing hydrogen absorption, enhancing hydrogen desorption, and/or enhancing hydrogen recombination.;The main scientific contribution is to interpret the effects of different inhibitors through the study of CH,diff and provide a protocol to computationally predict the effects of inhibitors on HEAC susceptibility with limited experiments. The engineering contribution is to identify two inhibitors, one cationic and one anionic, that can be delivered to crack tips from coatings to inhibit HEAC.
机译:低合金超高强度合金钢(UHSS)受氢环境辅助开裂(HEAC)的限制,限制了它们在海洋环境中的使用。在中等电位下观察到最低的HEAC敏感性。模型通过降低裂纹尖端的扩散氢浓度(CH,diff),增强阈值应力强度(KTH)和降低II期裂纹扩展速率(da / dtII)来解释这一点。本研究旨在通过使用水相抑制剂降低C H,diff来扩展降低的HEAC敏感性区域。;采用多方面的方法定量研究抑制剂对降低CH H diff的影响。在平面电极上在阳极电位的钼酸盐溶液中和在阴极电位的铈溶液中进行了初始测试;然而,较大尺寸的缝隙被用来测量局部电势和pH随施加电势和缝隙尺寸的变化。在阳极和阴极测试中,使用H吸收模型来预测局部C H,diff与局部电势,pH和比例因子的关系。使用微机械模型来预测抑制作用对HEAC敏感性的影响。结果与使用比例因子的实际尺寸裂纹有关。最后,进行了断裂实验,以验证通过综合研究方法获得的预测的KTH和da / dtII。钼酸盐的添加将da / dtII降低至1 nm / s,将还原的HEAC区域扩展至更多的阳极电位。缓解的增强可能是由于形成钼酸诱导的化学缓冲酸化作用之外的表面膜,这些表面膜更能抵抗裂纹尖端的溶解,从而降低了CH,diff。铈的添加在etaH = -0.35和-0.47 V时分别将da / dt II降低至9和32 nm / s,而在类似的阴极条件下,铈/铈的da / dt II在相同的阴极条件下分别降低至50和500 nm / s。铈化学形成不溶性膜,可通过减少氢吸收,增强氢解吸和/或增强氢重组来减少CH,diff 。;主要的科学贡献是通过研究CH,diff来解释不同抑制剂的作用并提供一种在有限的实验条件下通过计算预测抑制剂对HEAC敏感性影响的方案。工程上的贡献是确定了两种抑制剂,一种是阳离子型,另一种是阴离子型,可以从涂料中释放到裂纹尖端以抑制HEAC。

著录项

  • 作者

    Al-Ghamdi, Sami M.;

  • 作者单位

    University of Virginia.;

  • 授予单位 University of Virginia.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 348 p.
  • 总页数 348
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:36:56

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