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Electrochemical aspects of metal sulfide bioleaching and biocorrosion.

机译:金属硫化物生物浸出和生物腐蚀的电化学方面。

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摘要

The present study has investigated the electrochemical reactions involved in (a) the biooxidation of metal sulfides, such as pyrite (in relation to desulfurization of coal, extraction of uranium and gold from pyritic ores), copper from a chalcopyrite and zinc from a zinc sulfide flotation concentrate; and (b) the biocorrosion of stainless steel samples. Using cyclic voltammetry and carbon-paste-MS (metal sulfide) working electrodes, it was found that the oxidation of metal sulfides involved a large number of intermediate electrochemical reactions and/or the formation of non-stoichiometric compounds in the presence and absence of bacteria. The bacterial leaching processes were found to be solid-state diffusion controlled as suggested by the chronoamperometric and chronopotentiometric measurements. The activation energies associated with the solid-state diffusion of pyrite, chalcopyrite and zinc sulfide leachings were determined by the Sand's approach to be 22.4 kJ, 20.5 kJ and 21.3 kJ, respectively. These activation energies are in the order of magnitude of energies, which are typical for solid-state diffusion controlled reactions of semiconductor metal sulfides. The reaction mechanism of biooxidation of semiconductor metal sulfides was explained in terms of solid-state properties (energy density states) of metal sulfides and redox leach system.; The biocorrosion of stainless steel samples (304, 316 and 416 SS) indicated that the 416 SS sample containing the highest amount of sulfur (0.32%S) was the most corroded. In terms of initial rest potentials, it was found that the order of bacterial corrosion of SS samples: 416 SS {dollar}>{dollar} 304 SS {dollar}>{dollar} 316 SS was inversely proportional to their rest potentials {dollar}-{dollar}605 mV {dollar}<{dollar} {dollar}-{dollar}404 mV {dollar}<{dollar} {dollar}-{dollar}354 mV, respectively. For the stainless steel weldment samples, the percentage (%) of elongation (strain) and UTS (ultimate tensile strength) were found to be decreased, but their YS (yield strength) increased, as compared with the as received (no weldment) samples. After 5 days of biocorrosion, the 416 SS showed a significant decrease in the elongation, YS, and UTS.
机译:本研究研究了(a)黄铁矿(与煤的脱硫,黄铁矿中铀和金的提取有关),黄铜矿中的铜和硫化锌中的锌等金属硫化物的生物氧化所涉及的电化学反应。浮选精矿(b)不锈钢样品的生物腐蚀。使用循环伏安法和碳糊-MS(金属硫化物)工作电极,发现金属硫化物的氧化涉及大量的中间电化学反应和/或在存在和不存在细菌的情况下形成非化学计量的化合物。如计时安培法和计时电位法测量所表明的,发现细菌浸出过程是固态扩散控制的。通过Sand's方法确定的与黄铁矿,黄铜矿和硫化锌浸出的固态扩散相关的活化能分别为22.4 kJ,20.5 kJ和21.3 kJ。这些活化能为能量的数量级,这对于半导体金属硫化物的固态扩散控制的反应是典型的。用金属硫化物的固态性质(能量密度态)和氧化还原浸出系统解释了半导体金属硫化物的生物氧化反应机理。不锈钢样品(304、316和416 SS)的生物腐蚀表明,含硫量最高(0.32%S)的416 SS样品腐蚀最严重。就初始静止电位而言,发现SS样品的细菌腐蚀顺序为:416 SS {美元}> {美元} 304 SS {美元}> {美元} 316 SS与它们的静止电位成反比{美元} -分别为605 mV {dollar} <{dollar} {dollar}-{dollar} 404 mV {dollar} <{dollar} {dollar}-{dollar} 354 mV。对于不锈钢焊件样品,与不使用焊件的样品相比,伸长率(应变)和UTS(最终抗拉强度)的百分比(%)降低了,但其YS(屈服强度)却增加了。经过5天的生物腐蚀后,416 SS的伸长率,YS和UTS明显降低。

著录项

  • 作者

    Choi, Wan-Kyu.;

  • 作者单位

    New Mexico Institute of Mining and Technology.;

  • 授予单位 New Mexico Institute of Mining and Technology.;
  • 学科 Engineering Metallurgy.
  • 学位 Ph.D.
  • 年度 1990
  • 页码 191 p.
  • 总页数 191
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 冶金工业;
  • 关键词

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