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饮用水中痕量碘的离子色谱积分安培测定法 被引量:2

Determination of trace iodide in drinking water by ion chromatography coupled with integrated amperometric detection
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摘要 目的建立水中痕量碘的离子色谱分离积分安培检测法。方法采用IonPacASll亲水性阴离子交换柱,以40mmol/L氢氧化钠为淋洗液,通过向银工作电极上施加对应时间的循环电位进行积分安培检测。水样经0.22μm滤膜过滤,直接进样测定。结果碘离子的保留时间小于6min,在1.0-500μg/L浓度范围内,所得回归方程呈良好的线性关系,r=-0.9997。该方法的检出限为0.3μg/L,定量下量检测。限为1.0μg/L,RSD为1.8%,平均回收率在96.0%-103.5%。结论该方法的灵敏度高,操作简便,线性范围宽,准确可靠。 Objective To establish the method for determination of trace iodide in drinking water by ion chromatography coupled with integrated amperometric detection. Methods An anion exchange column, Ionpac AS11 column, was used, and 40 mmolfL NaOH solution was used as elute, iodide was separated and detected by integrated amperometry on a silver working electrode. After filtration by 0.22 μm filter, water samples could be injected directly. Results The retention time of iodide was less than 6 min. A good linear relationship was achieved in the range of 1.0-500 μg/L, r=0.999 7. The limit of detection was 0.3 μg/L and the limit of quantification was 1.0 μg/L. The relative standard deviation of the method for 10 μg/L iodide was 1.8%.The average recoveries for spiked samples were in the range of 96.0%-103.5%. Conclusion The method reveals several advantages including sensitivity, simplicity, broad linear range and accuracy, and it is applicable to the batch analysis of trace iodide in drinking water samples.
出处 《环境与健康杂志》 CAS CSCD 北大核心 2013年第11期1015-1016,共2页 Journal of Environment and Health
关键词 碘离子 色谱法 离子交换 积分安培 Iodide Chromatography, ion exchange Integrated amperometrie detection
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  • 1张贵珠,张海清,郭薇,何锡文,史慧明.荧光动力学法测定痕量硫氰根离子的研究[J].分析科学学报,1994,10(3):52-54. 被引量:22
  • 2刘崴,杨红霞,李冰,陈登云,张惠娟.高效液相色谱-电感耦合等离子体质谱测定地下水中碘形态稳定性[J].分析化学,2007,35(4):571-574. 被引量:34
  • 3王海燕,刘列钧,李淑华,谷云有,李秀维,王建强,李素梅.适合缺碘及高碘地区水碘检测的方法研究[J].中国地方病学杂志,2007,26(3):333-336. 被引量:130
  • 4[3]Frantisek S,Fréchet JMJ.Modified poly(glycidyl methacrylate-co-ethylene dimethacrylate)continuous rod columns for preparative-scale ion-exchange chromatography of proteins[J].Chromatogr A,1995,702:89-95.
  • 5BURGI H; SCHAFFNER T H, SEILER J P. The toxicology of iodate: A review of the literature[J]. Thyroid, 2001,11(5):449-456.
  • 6GILFEDDER B S, PETRI M, WESSELS M, et al. An iodine mass-balance for Lake constance, germany.. insights into iodine speciation changes and fluxes[J]. Geochimica et Cosmochimica Acta, 2010, 74.. 3090- 3111.
  • 7SCHWEHR K A, SANTSCCHI P H. Sensitive determination of iodine species, including organic-iodine for freshwater and seawater samples using high performance liquid chromatography and spectrophotometric detection[J]. Anal Chim Acta, 2003,482:59-71.
  • 8HONGLAN S, CRAIG A. Rapid IC-ICP-MS method for simultaneous analysis of iodoacetic acids, bromoacetic acids, bromate, and other related halogenated compounds in water[J].Talanta, 2009,79 : 523-527.
  • 9SHAH M, WUILLUID R G, S S, et al. Iodine speciation studies in commercially available seaweed by coupling different chromatographic techniques with UV and ICP-MS detection[J]. JAAS, 2005, 20:176-182.
  • 10CHEN Zu-liang, MEGHARAJ M, NAILDU R. Sepciation of iodate and iodide in seawater by non-suppressed ion chromatography with inductively coupled plasma mass spectrometry [J].Talanta, 2007, 72:1842-1846.

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