Amin Alaa S, Gouda Ayman A
Chemistry Department, Faculty of Science, Benha University, Benha, Egypt.
Talanta. 2008 Sep 15;76(5):1241-5. doi: 10.1016/j.talanta.2008.05.034. Epub 2008 Jul 7.
A new simple, very sensitive, selective and accurate procedure for the determination of trace amounts of iron(II) by solid-phase spectrophotometry (SPS) has been developed. The procedure is based on fixation of iron(II) as 2,3-dichloro-6-(3-carboxy-2-hydroxy-1-naphthylazo)quinoxaline on a styrene-divinylbenzene anion-exchange resin. The absorbance of resin sorbed iron(II) complex is measured directly at 743 and 830nm. Iron(III) was determined by difference measurements after reduction of iron(III) to iron(II) with hydroxylamine hydrochloride. Calibration is linear over the range 1.0-20 microgL(-1) of Fe(II) with relative standard deviation (R.S.D.) of 1.65% (n=10.0). The detection and quantification limits for 100mL sample system are 280 and 950 ngL(-1) using 0.5 g of the exchanger. The molar absorptivity and Sandell sensitivity are also calculated and found to be 2.86 x 10(6)Lmol(-1)cm(-1) and 0.0196 ngcm(-2), respectively. The proposed procedure has been successfully applied to determine iron(II) and iron(III) in tap, mineral and well water samples.
已开发出一种通过固相分光光度法(SPS)测定痕量铁(II)的新的简单、非常灵敏、选择性好且准确的方法。该方法基于将铁(II)以2,3-二氯-6-(3-羧基-2-羟基-1-萘基偶氮)喹喔啉的形式固定在苯乙烯-二乙烯基苯阴离子交换树脂上。直接在743和830nm处测量树脂吸附的铁(II)络合物的吸光度。用盐酸羟胺将铁(III)还原为铁(II)后,通过差值测量法测定铁(III)。在1.0 - 20 μg L⁻¹的Fe(II)范围内校准呈线性,相对标准偏差(R.S.D.)为1.65%(n = 10.0)。对于100mL样品体系,使用0.5g交换剂时,检测限和定量限分别为280和950 ng L⁻¹。还计算了摩尔吸光系数和桑德尔灵敏度,分别为2.86×10⁶ L mol⁻¹ cm⁻¹和0.0196 ng cm⁻²。所提出的方法已成功应用于测定自来水、矿泉水和井水样品中的铁(II)和铁(III)。