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The use of liquid chromatography for the analysis of metal ions in aqueous solutions and for the determination of water in organic matrices

机译:液相色谱法用于分析水溶液中的金属离子和测定有机基质中的水

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摘要

The value of a p-phenylenediammonium eluent in single-column ion chromatography is demonstrated. It is shown to be particularly useful for separating trivalent aluminum from common divalent metal ion interferences. The aluminum is detected with a conductivity detector;Postcolumn reaction in liquid chromatography is reviewed. The application of disodium 1-(2-thiazolylazo)-2-naphthol-3,6-disulfonate (TAN-3,6-S) to the detection of metal ions in single-column ion chromatography with a visible absorbance detector is explored. TAN-3,6-S is shown to complex a large number of metal ions. It is a particularly useful postcolumn reagent because by the judicious selection of effluent pH, selectivity may be introduced into the detection system;Temperature is shown to affect the retention times of divalent and trivalent metal ions in ion chromatography. Factors contributing to this phenomenon are examined, and enthalpy changes for several ion-exchange reactions are calculated and compared. Several chromatographic separations are improved by operating the system at elevated temperature;Two methods for the determination of water in organic matrices using liquid chromatography and a spectrophotometric detector are presented. Both employ a chromatographic separation by ion-exclusion. The first detection method makes use of solvatochromism, the shift in an organic spectrum which occurs as solvent polarity is changed. This second detection method uses a solid-phase postcolumn reactor containing a cation-exchange resin in the H[superscript]+ form. This reactor acts as catalyst for a reaction occurring between water and two components of the mobile phase, methanol and trans-cinnamaldehyde. In the reactor, an equilibrium is established between cinnamaldehyde and methanol, which form an acetal and water. The presence of water in a sample causes the equilibrium to shift back towards the cinnamaldehyde, causing an increase in absorbance when the spectrophotometric detector is set at a wavelength where cinnamaldehyde absorbs. ftn[superscript]1DOE Report IS-T-1373. This work was performed under contract No. W-7405-Eng-82 with the Department of Energy.
机译:说明了单柱离子色谱法中对苯二甲铵洗脱液的价值。已显示它对于从常见的二价金属离子干扰物中分离三价铝特别有用。用电导检测器检测铝;回顾液相色谱中的柱后反应。探索了1-(2-噻唑基偶氮)-2-萘酚-3,6-二磺酸钠(TAN-3,6-S)在可见光吸收检测器单柱离子色谱法中检测金属离子的应用。 TAN-3,6-S被证明与大量金属离子络合。它是一种特别有用的柱后试剂,因为通过明智地选择流出液pH,可以将选择性引入检测系统中;显示温度会影响离子色谱中二价和三价金属离子的保留时间。检查了导致这种现象的因素,并计算并比较了几种离子交换反应的焓变。通过在高温下操作该系统,可以改善一些色谱分离效果。提出了两种使用液相色谱法和分光光度检测器测定有机基质中水的方法。两者均通过离子排斥色谱分离。第一种检测方法利用溶剂致变色,即随着溶剂极性的改变而发生的有机光谱变化。该第二种检测方法使用包含H +形式的阳离子交换树脂的固相柱后反应器。该反应器充当水与流动相的两种组分甲醇和反肉桂醛之间发生的反应的催化剂。在反应器中,肉桂醛和甲醇之间形成了平衡,形成了乙缩醛和水。样品中水的存在会导致平衡向肉桂醛的方向移动,当分光光度检测器设置为肉桂醛吸收的波长时,吸光度会增加。 ftn [上标] 1DOE报告IS-T-1373。这项工作是根据与能源部签订的W-7405-Eng-82合同进行的。

著录项

  • 作者

    Fortier, Nancy Elaine;

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  • 年度 1988
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  • 原文格式 PDF
  • 正文语种 en
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