Pullin M J, Cabaniss S E
Department of Chemistry and Water Resources Research Institute, Kent State University, Kent, OH 44242, USA.
Water Res. 2001 Feb;35(2):363-72. doi: 10.1016/s0043-1354(00)00259-1.
An iron flow-injection analysis system has been optimized for the analysis of iron in waters high in dissolved organic carbon. The method detects either dissolved iron(II) or total dissolved iron with a detection limit of 10 nM, precision of 0.65% at 1 microM, and a dynamic range of four orders of magnitude. There are minimal interferences (< 1%) from other metals at environmental concentrations. The iron(II) method measures iron(II) in the presence of excess iron(III) with less than 1% interference. When used with pre-acidified samples, the total dissolved iron method agrees well with electrothermal atomic absorption spectrometry for a variety of natural waters with a range of dissolved organic carbon (3-36 mg C/L) and iron (1-28 microM) concentrations. When used with samples at their ambient pH, the total dissolved iron method detects dissolved iron, but not colloidal iron (size fraction 0.05-0.45 micron).
一种铁流动注射分析系统已针对溶解有机碳含量高的水中的铁分析进行了优化。该方法可检测溶解态铁(II)或总溶解态铁,检测限为10 nM,在1 microM时精密度为0.65%,动态范围为四个数量级。在环境浓度下,其他金属的干扰极小(<1%)。铁(II)方法在过量铁(III)存在的情况下测量铁(II),干扰小于1%。当与预酸化样品一起使用时,总溶解态铁方法与电热原子吸收光谱法对于各种具有不同溶解有机碳(3 - 36 mg C/L)和铁(1 - 28 microM)浓度的天然水结果吻合良好。当与处于环境pH值的样品一起使用时,总溶解态铁方法可检测溶解态铁,但不能检测胶体铁(粒径范围0.05 - 0.45微米)。