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Chemical speciation of iron in seawater by cathodic stripping voltammetry with dihydroxynaphthalene

机译:二羟基萘的阴极溶出伏安法测定海水中铁的化学形态

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The chemical speciation of iron in seawater is determined by cathodic stripping voltammetry using 2,3-dihydroxynaphthalene (DHN) as adsorptive and competing ligand. The optimized conditions include a DHN concentration of 0.5-1 mu M, seawater at its original pH of 8, and equilibration overnight. The cc-coefficient for DHN (=-[FeDHN]/[Fe']) was calibrated against EDTA giving values of 166 for 0.5 mu M DHN and 366 at 1 mu M DHN and a value of 8.51 +/- 0.07 for 109 K'(Fe'DHN). The dissociation of the natural iron species FeL was found to have a characteristic reaction time of 50 min, indicating that titrations should be equilibrated overnight rather than the shorter periods sometimes used onboard ship. The method was applied to samples from the Pacific giving ligand concentrations of 1.1 and 1.6 nM for deep and surface waters, respectively, with an average value for 109 K'(FeL) Of 11.9 +/- 0.3 compared to a value of 11.5 for the siderophore deferoxamine. The results are similar to those obtained previously for similar samples, but the new method has much greater sensitivity for iron than previous methods, leading to lower limits of detection and shorter analysis time.
机译:海水中铁的化学形态通过使用2,3-二羟基萘(DHN)作为吸附性和竞争性配体的阴极溶出伏安法测定。优化的条件包括DHN浓度为0.5-1μM,海水在其原始pH值为8且平衡过夜。针对EDTA对DHN的cc系数(=-[FeDHN] / [Fe'])进行校准,给出0.5μM DHN的166值和1μMDHN的366值以及109 K的8.51 +/- 0.07值'(Fe'DHN)。发现天然铁物种FeL的解离具有50分钟的特征性反应时间,这表明滴定应平衡过夜,而不是有时在船上使用的较短时间。该方法适用于太平洋地区的样品,深水和地表水的配体浓度分别为1.1和1.6 nM,109 K'(FeL)的平均值为11.9 +/- 0.3,而水合物的平均值为11.5。铁载体去铁胺。结果与以前从类似样品中获得的结果相似,但是新方法对铁的敏感性比以前的方法高得多,从而导致更低的检测限和更短的分析时间。

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